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Volume 21, 1888

II.—Zoology.

Art.. VIII.—On some Birds from the Kermadec Islands.

[Read before the Auckland Institute, 24th September, 1888.]

In my paper on the flora and fauna of the Kermadec Islands, printed in the recently-issued volume of “Transactions of the New Zealand Institute,”* I have given a list of the birds observed during my short stay in the group. Since then Captain Fairchild has made a second visit to the islands, and has obtained some additional specimens, which he has very kindly placed in my hands. Mr. Bell, the resident on Sunday Island, has also forwarded to the Museum a collection of birds' eggs, accompanied with some interesting particulars respecting several of the sea-birds which frequent the island for breeding purposes. From these sources of information I am now able to record the presence of two species new to the New Zealand fauna, and to prove that a third, hitherto only known as an occasional straggler in our waters, breeds regularly in the Kermadec group.

1. Sula cyanops, Sundevall (Masked Gannet).

In my list I briefly alluded to the presence of a fine gannet differing from the species common all round the North Island in wanting the buff-coloured feathers on the head. From the deck of the “Stella” it was noticed to be breeding in some numbers on the top of Curtis Island, but, as bad weather compelled Captain Fairchild to put out to sea before an ascent of the cliffs could be made, I was unable to procure a specimen. During his last visit, however, Captain Fairchild was more fortunate. He reached the summit of the island, and, finding the birds breeding there as before, caused four of them to be taken off their nests and carried on board the steamer. Thanks to his care, all four reached Auckland alive. On examining them it was evident that the species was that known as the masked gannet (Sula cyanops), which has a wide range in tropical seas, but had not been previously found on the coast of New Zealand. As mentioned above, it is at once distinguished from our common gannet (Sula serrator) by the head and neck of the adult bird being perfectly white,

[Footnote] * “Trans. N.Z. Inst.,” vol. xx., art. xxiii., pp. 163–5.

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and presenting no trace of the beautiful buff-yellow so conspicuous in Sula serrator. It is also rather smaller, and the shape and colour of the bare skin at the base of the bill are different. In the masked gannet the bare skin extends a little beyond the corners of the mouth, and then crosses the throat in an almost straight line, while its colour in the adult bird is a deep blackish-blue. This dark colour contrasts vividly with the snow-white feathers of the head and neck, and is doubtless the reason why the bird has received the common name of the “masked gannet.” In Sula serrator the bare skin is continued under the throat for a considerable distance in the shape of a narrow triangular stripe, and its colour is a pale leaden-blue.

Like our species, it forms no true nest. On Curtis Island its single egg was placed in a slight depression among the scanty tufts of short grass which form the chief vegetation on the top of the island. The females are quite exposed while sitting on the nest, and from their white plumage form very conspicuous objects; but, as they are strong and powerful birds, well able to defend themselves from all enemies, their exposed position is probably no real disadvantage to them.

Few birds have a wider geographical range. Drs. Finsch and Hartlaub, in their well-known book on the avifauna of Central Polynesia, state that it has been found in the following localities: The Atlantic Ocean, near Ascension Island; the Red Sea; Cocos Island; the Straits of Sunda; Torres Straits and North Australia; Polynesia, from the Sandwich Islands southwards to Samoa, and westwards from the Paumotu group to the New Hebrides. It seems probable that it also exists on the coasts of both North and South America.

2. Gygis candida (Silky White Tern).

While conversing with Mr. Bell respecting the birds of Sunday Island he alluded to a small white tern which visits the island every November to breed. From his description of the plumage, & c., and account of its breeding-habits, I concluded that it would probably prove to be this species. During the last breeding-season Mr. Bell made further notes on it, and has now sent me these, together with specimens of the egg. As his notes, and the shape, size, and colour of the egg agree exactly with the published accounts of Gygis candida, I have now no hesitation in considering it to be that species. The bird, which is a most beautiful one, is rather smaller than our common tern (Sterna frontalis). It has a slender body, long wings, and deeply-excised tail. The whole of the plumage is pure-white, and of silky softness. The bill is long and curved slightly upwards, dark-blue at the base, shading off into black at the tip. Its breeding-habits are peculiar. Mr.

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Cheeseman.—On Birds from the Kermadec Islands.

Bell writes, “It lays its solitary egg high up on the pohutukawa trees, on a horizontal branch not much thicker than a man's wrist. The bird sticks to the egg and keeps it in its place until it is hatched.” This statement is corroborated by what is known of its habits in some other localities. Mr. Cuming, the well-known conchologist, observed it on Elizabeth Island, and says, “It was breeding on a kind of pandanus, its single egg being deposited on the horizontal branches, in a depression which, although slight, was sufficient to retain it in position despite of the high winds and consequent oscillations to which it was subjected.” Mr. Cuming adds that the old birds were flying about in thousands like swarms of bees, and that he noticed several breeding on the same tree. Several young birds were observed lying dead on the ground, from which it appears that they frequently drop from their dangerous resting-place. However, it does not always breed on trees; for Dr. Graffe, a German collector, found it resting in hollows of the bare rock on one of the islands of the Phænix group.

Gygis candida is found throughout the whole of Polynesia, along the Australian coasts northwards to Torres Straits, and from thence through the Malay Archipelago to India. It has also been recorded from the west coast of Africa.

3. Phaeton rubricauda, Bodd (Red-tailed Tropic Bird).

This beautiful bird, so familiar to all voyagers in the warmer parts of Polynesia, has long been known to breed as near to New Zealand as Norfolk Island, and occasional stragglers are at long intervals captured by the Maoris residing near the North Cape, usually after a succession of heavy northerly gales. Few Europeans, however, have seen it in New Zealand waters, and the only specimen obtained, so far as I know, is one shot by Mr. Henry Mair near the Three Kings Islands, and now in the possession of Sir Walter Buller.

When at the Kermadec Islands last year Mr. Bell informed me that the tropic bird breeds regularly on Sunday Island, arriving in October and remaining until the close of summer. I therefore inserted the species in my list on his authority. I have now received from him several roughly-prepared skins and some eggs which prove that it has been correctly identified. Its appearance, habits, and geographical distribution are too well known to require mention here.

The following record of the temperature at Sunday Island in 1887–88 has been made by Mr. Bell, and forwarded by him to Mr. Percy Smith, Assistant Surveyor-General. As no meteorological observations of any kind have been pre-

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viously taken in the group, it is perhaps worth insertion here:—

I. Mean temperature in the shade, taken from daily observations made at 9 a.m.:—

°
January 77.4
February 74.6
March 74.9
April 69.4
May 68.1
June 65.0
July 62.1
August 64.0
September 68.5
October 68.3
November 72.6
December 75.3
Mean for the year, 70°.

II. Occasional readings of the thermometer taken at noon:—

Shade. Sun.
Jan. 3 85 107
" 5 87 110
" 15 88 104
" 16 89 Cloudy
" 17 91 110
" 18 91 110
" 19 94 111
" 20 94 112
" 22 95 120
" 25 90 114
" 31 88 Cloudy
Feb. 9 85 100
" 11 90 108
" 16 87 104
" 27 86 102
Mar. 16 85 101
" 20 87 100
June 14 70 90
" 22 70 89
July 1 69 87
" 29 67 90
Nov. 14 84 94
" 22 94 104
Dec. 4 85 102
" 12 83 106
" 19 87 102
" 24 84 100
" 28 89 100
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Art. IX.—Notice of the Capture of a Specimen of the Shy Albatross (Diomedea cauta) near Auckland.

[Read before the Auckland Institute, 2nd July, 1888.]

So far as I am aware, only two instances are on record of this rare bird being obtained in New Zealand. Some time in 1876 a specimen was captured in Blueskin Bay, Otago, and came into the possession of Professor Hutton, who was at that time in charge of the Otago Museum. Professor Hutton identified it as the Shy Albatross, or Diomedea cauta; and I believe the specimen still exists in the collections of the Museum. In July, 1887, another example came ashore near the pilot-station, at the entrance to Wellington Harbour. It was secured by some fishermen, and ultimately passed into the hands of Dr. (now Sir Walter) Buller. In the tenth volume of the “Transactions” an account will be found of the circumstance, and a full description of the bird.*

About six weeks ago Mr. D. Bate, of Brighton, Parnell, informed me that he had an albatross differing in plumage from any of the stuffed examples in the Museum. On calling to see it, I found that it was undoubtedly a male, in full plumage, of the Shy Albatross. Mr. Bate informed me that a friend of his, while shooting curlew by the side of the Manukau Harbour, near Penrose, observed the bird in a grasspaddock. Albatrosses are unable to take flight from a level piece of ground, so that there was no difficulty in approaching it; in fact, it could do little more than waddle about in a circle. Concluding that it was injured, an attempt was made to seize it by the neck. This was evidently done in a most incautious manner, for I am informed that the bird retaliated by seizing its assailant by the lower part of the nose, inflicting a severe tear. However, it was at length captured and despatched. Mr. Bate has kindly presented the specimen to the Museum, so that I am able to exhibit it to you this evening.

The Shy Albatross is easily distinguished from all the other species by the beautiful pearl-grey feathers of the face and neck, and by a narrow yellow line at the base of the bill. This latter character can only be observed in living specimens, although conspicuous enough in them; the membrane soon losing its colour after death. Very little is known of its habits. Unlike the other species it is not at all bold, and seldom approaches ships. Nothing is known of its breeding-places, nest, or eggs. Mr. Gould, the author of the “Birds of Aus-

[Footnote] *“Trans. N.Z. Inst.,” vol. x., art. xxv., p. 217.

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tralia conjectures that it may breed on the Mewstone and some other small islands to the south of Tasmania, from the fact that adult birds are commonly seen in the neighbourhood during the spring months; but up to the present time this supposition has not been verified. It will be interesting to ascertain whether the few specimens caught off our shores have come from a breeding-station to the south of New Zealand, or have wandered across from Tasmania.

Art. X.—The Habits and Home of the Wandering Albatross

(Diomedea exulans).

[Read before the Auckland Institute, 2nd July, 1888.]

This noble bird may justly be called the king among the sea-birds. Many times during my sea-voyages have I admired its flight and easy sailing over the waves, as it followed our vessel, hundreds of miles from the nearest land. Its power of flight surpasses that of most birds, and is easily accounted for by the unusual development of the muscles of the breast and wings, the latter being equal to, if not stronger than, those of the eagle. It is worthy of remark that the quills of the wing are spread or brought close together according as the bird is rising or falling in its flight. The steering is done not with the tail alone, but also with the broad webbed feet. These, when a straight course is being followed, are stretched out, and nearly concealed under the tail; but when a quick turn is required their position is altered, and the webs are spread in such a manner as to greatly assist the bird in turning. When there is little wind and the ocean is calm, albatrosses have great difficulty in rising from the water; when there is a swell they run along the water and rise with a wave. When alighting, on nearing the surface they bend the head back, curve the wings upwards, beating the air with numerous laboured strokes, then, straightening their feet, they let themselves fall. They are fast swimmers, but cannot dive. Their food, which consists chiefly of some of the lower forms of marine life found floating on the surface of the ocean, they scoop up with their bill in the same manner as the ducks.

I had long been anxious to visit their breeding-haunts, but had no opportunity of doing this until January, 1888, when I was afforded the privilege of accompanying the Government steamer “Stella” on her yearly cruise among the islands to the south of New Zealand. After visiting Stewart Island and the Snares, the steamer's course was directed towards the

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Auckland Islands, and on the 25th January we anchored in Carnley Harbour. Having ascertained from Captain Fairchild that the vessel would not leave until the following evening, I at once prepared for an expedition to the hills, on which I was informed that albatrosses were then breeding; and at 4 o'clock in the morning the chief officer put me ashore. The first creatures I met were several sea-lions sleeping in the long grass, over which I almost fell. They gave discontented growls at being disturbed and driven from their lair, sitting up on their haunches and gazing at the intruder with their large eyes, showing their white canine teeth all the time. Moving onwards I had a dreadful scramble through dense low scrub interspersed with holes and swampy places, but at last I gained the hills above. My exertions caused me to suffer greatly, being far from well through overwork on the west coast of the South Island. After climbing over hills for about three miles I came to a slope where a colony of albatrosses had established a breeding-place. The birds were scattered about among the tussock-grass, sitting on their nests, and from their white plumage could be easily distinguished from the vegetation at a great distance. I found that their nests are always placed on sloping ground, and always on the most exposed side of the hill. They are composed of earth and grass cemented together, and are built in the form of a cone. They are usually about 2ft. in diameter and about 18in. high. Outside they are surrounded by a shallow drain, intended to carry off the surface-water. Within is placed a single egg. This is white, with a few brown spots on the broad end, and measures about 5·5in. in length by 3·lin. broad. In most cases I found the female on the nest, the male bird standing close to her, and occasionally feeding her. I noticed that sometimes the male relieved the female, but they never both leave the nest until the young one is able to defend itself against the skua gull (Lestris parasiticus). This rapacious bird devours every egg or nestling left unprotected. While taking the measurements of the first nest I came to I laid down the egg beside me, when a skua darted at it and destroyed it. They were so bold that they frequently came close enough for me to hit them with a stick.

On my approaching an albatross's nest the old bird seldom left it, but set up a croaking noise, clapping its mandibles together and biting at the intruder. After turning it off and taking away the egg, it returned and sat on the nest as before. The eggs were quite fresh on the 25th January, and good for eating when fried. There appears to be a difference in the time of laying at the different islands, for at Campbell Island, considerably to the south of the Auckland Islands, their eggs

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were nearly all hatched by the end of January, while at Antipodes Island, a little to the north again, they had hardly begun to lay at the beginning of February. In all these three islands albatrosses are most plentiful.

The albatross takes five years to become fully mature, and in each year there is a slight change of plumage. The young, which are hatched in February, are covered with snow-white down, and a beautiful specimen in this stage exists in the Otago Museum. In the following December they lose their down, and the plumage is of a brown colour, with white under the wings and on the throat. In the second year the plumage is the same except that there is more white on the throat and abdomen. In the third year there is still more white, although mixed with blotches of brown, the under parts, however, being nearly all white. The wings and tail remain dark-brown. In the fourth year they very nearly acquire the full plumage. The male is white with a few very fine dark specks, except the wings, which are dark-brown. In the fifth year they reach their full growth, and the mature plumage is displayed—white, with blackish-brown wings. The measurements are as follows: Total length from the tip of the bill to the end of the tail, 3ft. 3in. Bill, 7in. Tail, 7·25in. Whole wing, from 4ft. 10in. to 5ft. 10in.; primaries, 1ft. 8in. Whole leg, 1ft. 10½in.; tarsus, 4·5in.; middle toe, 7in. The female is much smaller, as can be seen at once from the specimens exhibited.

Notwithstanding the ease and grace of the albatross on the ocean, on the land it is a most clumsy and helpless bird. Its walk is slow and waddling, like that of a duck, and it cannot take flight from a level piece of ground. It is for this reason that these birds have been gifted by nature with the instinct of making their nests on the slopes of mountains, for by running down-hill, and labouring hard with their wings, they can at last acquire momentum sufficient to raise themselves in the air. Once there they exhibit their true power, and are seen to the best advantage.

Art. XI.—On a Specimen of the Brown Gannet (Sula fusca) shot in Napier Harbour, with Notes on other New Zealand Birds.

[Read before the Hawke's Bay Philosophical Institute, 9th July, 1888.]

It is my good fortune to be able to record the occurrence of a bird which to the best of my belief has not yet been observed in New Zealand, although the remarkable part of the

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matter is not the stranger's visit, but that it has not been recorded before this, for the Brown Gannet, or Booby (Sula fusca) has been obtained in nearly all the temperate regions of the globe, in many cases doubtless as a straggler; but now a specimen has been shot here in the bay, and is before you this evening very nicely preserved by Mr. Yuille. Mr. Smith, of the Masonic Hotel, has added the specimen to his collection, which is becoming extremely interesting and valuable. I have had considerable trouble in looking up any description of this species, which is common in the Atlantic, but at last found a good account in a work by Lathom, published in 1785, rather more than a hundred years ago. This I have transcribed, and have added a few particulars from other sources respecting the habits of the bird.

Lathom's “General Synopsis of Birds” (1785), Vol. iii., Pt. 2, p. 612. Common Booby:—

Pelecanus Sula. Lin. Syst., 1, p. 218, 7.

Le Fou. Briss. Orn., vi., p. 495, 1; Buf. Ois., viii., p. 368, pl. 29. Anseri Bassano congener fusca avis. Raü. Syn., p. 191, 6; Sloan, Jam., p. 322., t. 271, fig. 2.

Booby. Brown, Jam., p. 481; Catesby, Car. 1, pl. 87.

Description.—Size of the lesser gannet: length, 2ft. 6in. The bill nearly 4½in. long, toothed on the edges, and of a grey colour; base of it pale-brown; space round the eyes, and the chin, bare of feathers, and covered with a yellowish skin; irides pale-grey; the head, neck, upper parts of the body, wings and tail, cinereous-brown; the greater quills much the darkest; the tail brownish at the end, and in shape greatly cuneiform; the breast, belly, thighs, and vent white; legs pale-yellow; claws grey.

Catesby observes that these vary—some have white bellies, and others not—and that there is no perceivable difference between male and female. The young birds have the head and neck white, with a slight tinge of brown; but may be distinguished from having the feathers of those parts downy and soft, and not the usual texture.

Place.—Inhabits the Bahama Islands; and we believe likewise very common in many other parts of the world. One specimen came from Cayenne. It probably may be the sort mentioned by Dampier as being so plentiful in the Island of Aves, eight or nine leagues east of Buenos Ayres, which is described as a very simple creature, that will hardly go out of a man's way. These are said to build their nests on the ground in places where no trees grow, but make them on the last whenever they can be found. The flesh is black and fishy, yet is often eaten by the privateers. Is also met with in New Guinea.* This has been seen at Kamtschatka; is found in the Faeroe Isles; and has also been met with on our own coasts [England] a few years since.

The term “booby” is applied by navigators more particularly to the Brown Gannet (Sula fusca), which inhabits the desolate islands and coasts where the climate is warm, or even temperate, throughout the greater part of the globe. The apparent

[Footnote] * Bosman. “A New Description of the Coast of Guinea.” 1721.

[Footnote] † Ellis., Nar., ii., p. 189.

[Footnote] ‡ “Arctic Zoology,” by Thos. Pennant. 1784.

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parent stupidity of the boobies is proverbial: calmly waiting to be knocked on the head as they sit on shore, or perching on the yard of a ship till the sailor climbs to their resting-place and takes them off with his hand, they fall a prey to the most artless birdcatcher. Even Byron's shipwrecked wretches, though—

Stagnant on the sea,
They lay like carcasses,

“caught two boobies and a noddy;” and the incident actually did occur in Bligh's celebrated voyage consequent on the mutiny on board the “Bounty,” when he and his boat's crew were in a most deplorable state. “Monday, the 25th,” says Bligh, “at noon, some noddies came so near to us that one of them was caught by hand… In the evening, several boobies flying very near to us, we had the good fortune to catch one of them… I directed the bird to be killed for supper, and the blood to be given to three of the people who were most distressed for food; the body, beak, and feet I divided into eighteen shares… Tuesday, 26th, we caught another booby; so that Providence appeared to be relieving our wants in a most extraordinary manner. The people were overjoyed at this addition to their dinner, which was distributed in the same manner as on the preceding evening, giving the blood to those who were the most in want of food.”

Dampier says that on the Alcranes Islands (Alacranes), on the coast of Yucatan, the crowds of these birds were so great that he could not pass their haunts without being incommoded by their pecking. He observed that they were arranged in pairs, and conjectured that they were male and female. He succeeded in making some fly away by the blows he bestowed on them, but the greater part remained in spite of his efforts to compel them to take flight.

De Gennes, in his voyage to the Straits of Maghellan, says that in the Island of Ascension there were such quantities of boobies that the sailors killed five or six at a time with one blow of a stick.

The Vicomte de Querhoent says that the French soldiers killed an immense quantity on this same island, and that their loud cries when disturbed at night were quite overpowering.

This apparent exception to the general rule of self-preserving instinct is so remarkable that we are led to look for some cause, and perhaps this may be found in the structure of the animal; for, according to many writers whose veracity cannot be doubted, the boobies stay to be taken and killed after they have become familiar with the effect produced by the blows or shots of their persecutors.

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In the case of most animals which, from not knowing his power, have suffered man to approach them to their destruction, alarm has been soon taken, the idea of danger has been speedily associated with his appearance, and safety has been sought in flight; but the wings of the booby are so long and its legs so short that, when once at rest on level ground, the bird has great difficulty in bringing the former into action, and when so surprised it has no resource but to put on a show of resistance with its beak, which is, to be sure, generally despised by its persecutor.

In the cases recorded by Bligh the birds were probably fatigued by wandering too far from the rocky shores which are their ordinary haunts. There they are generally to be seen constantly on the wing over the waves which beat at the foot of the crags, intent on fishing.

Though so well furnished with oars they are said to swim but seldom or never to dive. Their mode of taking their prey is by dashing down from on high with unerring aim upon those fishes which frequent the surface, and instantly rising again in the air. They walk with difficulty, and when at rest on land their attitude is nearly vertical, and they lean on the stiff feathers of the tail, like the cormorants, as a third point of support. The ledges of rocks or cliffs covered with herbage are the places generally selected for the nest, and there in great companies they lay their eggs, each hen bird laying from two to three. The young birds for some days after hatching are covered with a down so long and thick that they resemble powder-puffs made of swan's down.

The boobies seldom wander more than twenty leagues from land, to which they usually return every evening; and their appearance is considered by mariners as a sure token of their vicinity to some island or coast.

The colour of the Sula fusca, or Brown Booby, is blackish-brown or ashy-brown above and whitish beneath; the primaries are black, and the naked skin about the head is reddish; the orbits and base of the bill are yellow, and the point of the bill is brown; the legs are of a straw-colour. In length the brown booby is about 2ft. 5in, the bill measures 4½in. or thereabout, and the tail 10in. The young birds are spotted with white and brown.

It is almost impossible to open the pages of the old voyagers who have fallen in with these boobies without finding some accounts of the constant persecution to which the latter are subjected by the frigate or man-of-war birds.

Lesson, indeed, doubts this. He says, “The boobies have been so named because it has been supposed that the frigates compel them to disgorge the fish which they had taken; but this appears to me to be erroneous. The booby is

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warlike, he lives fearlessly near the frigate, and swallows the fish which he has captured in peace.”

Cuvier, Buffon, and Temminck, on the contrary, give credence to the narratives of the frigate's persecution, and, indeed, it is difficult to believe that so many eye-witnesses should be mistaken.

Feuillée says, “I have had the pleasure of seeing the frigates give chase to the boobies. When they return in bands in the evening from their fishing the frigates are in waiting, and, dashing upon them, compel them all to cry for succour, as it were, and in crying to disgorge some of the fish they are carrying to their young ones. Thus do the frigates profit by the fishing of the boobies, which they then leave to pursue their way home.”

Legnat, in his Voyage, writes thus: “The boobies come to repose at night upon the Island Rodriguez, and the frigates, which are huge birds, so called from their lightness and speed in sailing through the air, wait for the boobies every evening on the tops of the trees. They rise, on the approach of the latter, very high in the air, and dash down upon them like a falcon on his prey, not to kill them, but to make them disgorge. The booby struck in this manner by the frigate gives up his fish, which the frigate catches in the air. The booby often shrieks, and shows his unwillingness to abandon his prey; but the frigate mocks at his cries, and, rising, dashes down upon him anew till he has compelled the booby to obey.”

William Dampier observes that he remarked that the man-of-war birds and the boobies always left sentinels near their young ones, especially while the old birds were gone to sea on their fishing-expeditions, and that there were a great number of sick or crippled man-of-war birds which appeared to be no longer in a state to go out for provisions. They dwelt not with the rest of their species, and, whether they were excluded from their society or had separated themselves voluntarily, they were dispersed in various places, waiting apparently for an opportunity of pillage. He adds that one day he saw more than twenty on one of the islands (the Alcranes), which from time to time made sorties to procure booty. The man-of-war bird that surprised a young booby without its guard gave it a great peck upon the back to make it disgorge—which it instantly did—a fish or two as big as one's wrist, which the old man-of-war bird quickly swallowed. He further speaks of the persecution of the parent boobies by the able-bodied frigate-bird, and says that he himself saw a frigate fly right against a booby, and with one blow of its bill make the booby give up a fish just swallowed, upon which the frigate darted with such celerity that he seized it before it reached the water.

Catesby and others mention seeing similar encounters.

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Nuttall says, “The boobies have a domestic enemy more steady though less sanguine in his persecutions than man: this is the frigate pelican, who, with a keen eye descrying his humble vassal at a distance, pursues him without intermission, and obliges him by blows with his wings and bill to surrender his finny prey, which the pirate instantly seizes and swallows.”

The booby utters a loud cry, something between that of the raven and the goose; and this is heard more particularly when they are pursued or when, assembled together, they are seized with a sudden panic. Their nests, according to Dampier, are built in trees in the Isle of Aves, though they have been observed in other places to nestle on the ground. They always associate in numbers on the same spot, and lay one or two eggs. The young are covered with a very soft down. Nuttall says that they abound on the rocky islets off the coast of Cayenne and along the shores of New Spain and Carraccas, as well as in Brazil and the Bahamas, where they are said to breed almost every month in the year. In summer they are not uncommon on the coast of the Southern States of North America. The flesh he describes as black and unsavoury.

2. Ardea novæ-hollandiæ.

The White-fronted Heron.—This species is not nearly so common as the Common Blue Heron (Ardea sacra), and I have not seen a specimen for many years; but the one now before you was killed at Waipawa in May last. It is now in the collection of Mr. Smith, of the Masonic Hotel in this town.

3. Anthornis melanura.

The Bell-bird has almost disappeared from Hawke's Bay and the Seventy-mile Bush for some years. The specimen before you was procured at Takapau, and the sender informs me that they are once more appearing in that district.

4. Eudynamis.

Amongst a collection of New Zealand bird-skins sent to the Museum I found a skin of what appeared to be Eudynamis with the long tail-feathers imperfect, some not fully grown. On taking up the bird to ticket it, I saw that the breast, instead of the usual brown marks, was distinctly transversely barred with black metallic bars, as in the Bronze Cuckoo (Chrysococcyx). These bars extend from the beak to the vent. The bill is less robust than Eudynamis. The feet are light in colour, like those of an albino specimen. It has certainly the character of Eudynamis when seen from the back; but from the under side it suggests a cross between Eudynamis and Chrysococcyx.

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5. Ocydromus (albino).

We have in the Museum a beautiful specimen of a weka, snow-white with the exception of a few feathers on the back and at the base of the tail: these are of the usual colour. The legs were of a light-pink or flesh-colour, and much thinner in proportion than in ordinary. Caught at Mohaka.

6. Carpophaga novæ-zealandiæ (albino).

A curious variety of the New Zealand Pigeon was sent to me by Mr. Harding from Castle Point. The plumage is of a dirty-white colour, many of the feathers on the neck and shoulders being tipped irregularly with a ferruginous-brown colour.

Art. XII.—On new Species of Araneidea.

[Read before the Auckland Institute, 22nd October, 1888.]

Fam. Theridiidæ.

Genus Linyphia, Latr.

Linyphia purpura-punctata, sp. nov.

Male.—Ceph. th., long, 1·2; broad, 1. Abd., long, 1·8; broad, 1·2. Legs, 1, 2, 4, 3 = 6·8, 5, 4, 2·7 mm.

Cephalothorax yellow - brown, olive - brown dorsal band bifurcates from base of caput, connecting posterior central and lateral eyes; rugulose; oval, slightly compressed forwards; pars cephalica moderately convex, roundly truncated; thoracic fovea somewhat oval, caput and radial striæ moderately defined; profile-contour rises at an angle of about 35° from thoracic junction, somewhat horizontal across pars cephalica, dips forwards from posterior row of eyes; clypeus vertical, height nearly equals diameter of a fore-lateral eye.

Eyes on black spots; posterior row moderately recurved, central pair separated from each other by a space equal to rather more than their diameter, rather less than that interval from side-eyes next to them, two-thirds their space from anterior-centrals; fore-row recurved, median pair, smallest of eight, their diameter from each other, less than their radius from side-eyes; interval between lateral eyes rather exceeds interspace between posterior-centrals; seated obliquely on low eminences.

Legs yellowish, faint annulations on tibiæ and metatarsi; fairly stout; black hairs, long spines, on femoral, genual, tibial, and metatarsal joints, except metatarsi of 1–2.

Palpi, humeral, cubital, and radial joints pale straw-colour,

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former article one-third longer than two latter together; cubital joint somewhat linear, radial rather shorter than cubital, viewed from above somewhat cup-shaped; digital joint large, globose; springing from near articulation of joint is a brownish, irregular, triangular, semi-detached process, at extremity nearly as broad as long, fore-angles prolonged into two apophyses, outer black-brown, stout, pointed; inner longest, membranous, lake-brown, concave within; side-face of bulb spiral, glossy, outer circle broad, pale; inner circle red-mahogany; beneath the dark-brown, membranous, free apex is a black, pointed process; lamina bulbi broad-ovate, placed rather beneath bulbus, hairs rather sparse.

Falces brownish-yellow; conical, project moderately at base in front, directed rather forwards, exceed humeral joint of palpus in length.

Maxillæ yellowish-brown; fore-part broad, rounded, inclined towards labium, which is dark chocolate-brown; oval one-third broader than long, strongly everted.

Sternum cordate; yellow-brown, dark margin.

Abdomen oviform; ground-colour umber-brown, series of pinkish, purple-tinted flecks on either side of dorsal band, which is less defined than females, dark-brown near spinners; ventral surface brownish.

Female.—Geph. th., long, 1; broad, 1. Abd., long, 2·1; broad, 1·8. Legs, 1, 2, 4, 3 = 6·5, 5, 4, 3 mm.

Cephalothorax yellowish-brown, dorsal band and marginal zone olive-brown, former commences at thoracic fovea, bifurcating above junction of caput, to posterior eyes; glabrous; oval, moderately compressed forwards; pars cephalica convex, rounded, lateral index about equal to space between a hind-lateral eye and the hind-central furthest from it; fovea somewhat oval, caput groove and radial striæ moderately defined; profile-line rises slightly across ocular area, somewhat level to limit of caput, slopes moderately to base; clypeus vertical, height rather exceeds diameter of a fore-lateral eye.

Eyes on black eminences, laterals most prominent; posterior row moderately recurved, of about equal size, nearly equidistant, central eyes separated by an interval equal to their diameter and a quarter, about one-third less than their space from fore-centrals; anterior row recurved, median pair about one-third size of laterals, scarcely their breadth apart, about that interval from side-eyes; interspace between laterals rather exceeds that between posterior median pair.

Legs shade lighter than cephalothorax, rather faint annulations on tibiæ and metatarsi; moderately slender; black hairs, long, slender spines.

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Palpi pale yellow-brown; slender, about length of cephalothorax; armature, hairs, and bristles.

Falces and cephalothorax concolorous; conical, directed rather forwards, project somewhat in front at base; fangs small, reddish-brown.

Maxillæ, fore-half broad, convex, rounded, moderately inclined towards labium, yellow-brown. Lip one-third broader than long, recurved; chocolate-brown, margin pale.

Sternum yellowish-brown; cordate.

Abdomen oviform; umber-brown, flecked with large and small pinkish, purple-tinted, somewhat metallic spots; dorsal band brown, sinuate margins, posterior two-thirds narrower and darker; lateral margins dark-brown, few purple streaks and flecks; ventral surface displays a brown purple-margined, shield-shaped mark; abdomen sparsely clothed with short blackish hairs. Corpus vulvæ chestnut-brown; moderately prominent; represents a transverse area divided by a glossy, brown, rather narrow, x-shaped septum, whose base is prolonged, horizontally, on the tumid margins of foveæ.

Several specimens, Wairongomai Gorge, A. T. U.

Linyphia nitidulum, sp. nov.

Female.—Ceph. th., long, 1·6; broad, 1. Abd., long, 2; broad, 1·8. Legs, 1, 2, 4, 3 = 5·9, 4·9, 4·2, 2·2 mm.

Cephalothorax brownish-yellow, median band and marginal zone dark-olive; former broad, bifurcates forwards from base of caput; areolate; oval, moderately compressed forwards, pars cephalica somewhat depressed, roundly truncated; lateral index equal to space from a hind-lateral eye to the hind-central furthest from it; thoracic indentation not clearly defined, caput and radial striæ well marked; contour of profile rises slightly across pars cephalica to hind row of eyes, dips somewhat abruptly backwards; depth of clypeus equals diameter of a fore-lateral eye, directed sensibly inwards.

Eyes on black spots, anterior and posterior rows recurved, latter moderately; hind row about equidistant, central pair scarcely their breadth apart, more than twice their diameter from fore-centrals, which are about their breadth from each other and side-eyes next to them; lateral eyes sensibly larger than posterior-centrals, more than one-third larger than fore-median pair; seated obliquely, their diameter and a half from one another, on tubercular eminences, fore-pair strong.

Legs and cephalothorax concolorous, femora faintly clouded, tibiæ and metatarsi annulated with an olive tint; slender; armature, few black hairs and bristle-like spines.

Palpi colour of legs, moderately strong.

Falces light amber-colour; somewhat conical, directed visibly inwards.

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Maxillæ brownish-yellow; basal half longitudinally indented; fore-end rounded, tumid; inclined outwards; strong fringe of hairs. Labium chocolate-brown; oval, more than twice as broad as long, everted; about one-fourth as long as maxillæ.

Sternum brownish-yellow, margins clouded; coarse black hairs; cordate; slight eminences opposite coxæ.

Abdomen ovoid, fore-end pointed, projects over base of cephalothorax, lateral margins longitudinally corrugated; dorsal field creamy-brown, flecks of a paler hue; median mark broad, yellow margins, irregularly acutely crenate, extends from base to spinners, fore-half numerous pale flecks, few brown, somewhat angular marks on margin; posterior half maroon-colour; sides brownish, longitudinally streaked with dark olive-brown, margins yellow. Ventral surface brownish-yellow; displays a somewhat ovate, olive-coloured mark, two yellow spots. Corpus vulvæ amber-colour, speckled, glossy, somewhat oval, moderately prominent, transverse eminence, centrally produced into a longitudinal costa, at base of latter is a shallow, cuneate depression, with lake-coloured margins; fore-part concave within and prolonged above into a short, rather broad septum, which loops up a long, narrow, transverse membrane, projecting outwards above the rima genitalis; septum and membrane have glossy-brown, beaded margins.

This rather handsome specimen was captured amongst the light bush on the summit of Te Aroha. A. T. U.

Linyphia rufo-lineata, sp. nov.

Male.—Ceph. th., long, 2·8; broad, 2. Abd., long, 3·2; broad, 2. Legs, 1, 2, 4, 3 = 21, 13·1, 9, 7 mm.

Cephalothorax light yellow-brown; on posterior slope of pars cephalica is an olive-brown, lanceolate mark, which bifurcates forwards to posterior-lateral eyes; lateral margin of caput displays a longitudinal streak of similar hue; almost glabrous; rugulose; oval; moderately compressed forwards; caput moderately convex, lateral index nearly equals breadth at posterior row of eyes; median indentation on pars thoracica longitudinal, deep; caput and radial striæ well-defined; profile - contour represents a moderate double arch; clypeus vertical, height equal to more than diameter of a fore-central eye.

Eyes large, of almost equal size; posterior row procurved, centrals visibly the largest of eight, placed on black oval spots, three-fourths their diameter apart, separated by an interval equal to one-third their breadth from side-eyes next to them; anterior row recurved, median pair seated on a moderate black eminence, three-fourths their diameter from each other,

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their breadth and a quarter from hind-centrals; separated by a space equal to one-fourth their diameter from side-eyes; laterals seated obliquely, close together, on separate, black, tubercular eminences.

Legs and cephalothorax concolorous; red-chestnut annuli on all joints; light hairs; long, slender spines on femoral, genual, tibial, and metatarsal joints.

Palpi colour of legs; long; humeral joint rather exceeds cubital and radial in length; cubital joint about one-fourth shorter than radial, fore-third angular, furnished with a long bristle; fore-third of radial joint sharply constricted, margin tumid, brownish; projects two long, moderately - strong bristles; clava large; projecting from beneath the lip-like margin of the radial joint is a large yellow-brown, hairy process, terminal half compressed, somewhat quadrilateral, margin blackish; above latter process a long, stout, tapering, amber-coloured apophysis, furnished with short hairs, projects forwards from beneath a black-brown, acute-crenate, membranous fringe; projecting upwards and outwards from between the two latter organs is a short, stout, curved, pale amber-coloured process, concave beneath; bulbus genitalis somewhat spiral, apex membranous, broad, linear, rounded, concave, reddish-brown; projecting outwards at a right angle from base of contracted apex is a broad, acutely-pointed, reddish, membranous process; projecting from within concavity at bulbus are two stout, glossy-black apophyses; base of outer one broad, depressed in centre, fore-part compressed and rounded; lamina bulbi beneath bulb, apex pointed; moderately hairy.

Falces light mahogany-brown; transversely rugose; vertical; fore-third remarkably concave on outer side; equal in length to humeral joint of palpus.

Maxillæ broadest and slightly rounded at extremity; moderately inclined towards each other; brownish-yellow, base suffused with brown. Labium somewhat oval, short, everted; base chocolate-brown, margin yellowish.

Sternum brownish; somewhat cordate; eminences opposite coxæ.

Abdomen oviform, indentation above pedicel; yellowish-olive, numerous yellowish flecks; folium ovate, base dark-olive; a pale ⊥-shaped mark extends backwards from cleft; nearly in centre of abdomen are two closely-connected, somewhat oval, creamy-white transverse marks; margins red, less pronounced on posterior side, with an outer border of dark olive-brown; prolonged margins terminate with white spots; between oval marks and basal ⊥-shaped mark are two whitish sinuating lines; on posterior half of dorsal line is a not-well-defined, yellow-flecked, tapering streak, bifurcating forwards

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to oval marks; between latter marks and spinners are a series of three transverse, oblique, more or less pronounced, dark bars, fore-pair terminate with a white spot. Ventral surface yellowish; shield brown.

Female.—Ceph. th., long, 2·8; broad, 2. Abd., long, 4; broad, 3·2. Legs, 1, 2, 4, 3=14, 10, 8, 6 mm.

Cephalothorax brownish-yellow; dorsal mark olive-brown; somewhat fan-shaped on base of pars cephalica, compressed across pars thoracica; rugulose; almost glabrous; oval, moderately compressed forwards, lateral index exceeds breadth of eye-area; normal grooves fairly marked, fovea deep, somewhat circular; profile-line represents a moderate double arch; clypeus in height rather exceeds diameter and a half of a fore-central eye.

Posterior row of eyes procurved, sensibly exceed fore-row in size; centrals on black, oval spots, separated by an interval scarcely equal to their diameter, half that space from laterals next to them, their breadth and a half from fore-centrals; anterior row recurved; median pair seated on slight prominences, interspace rather exceeds their breadth, separated by scarcely their diameter from side-eyes; laterals seated obliquely, one-fourth their breadth apart, on dark, tubercular eminences.

Legs brownish-yellow, more or less defined brown annulations; slender; yellowish hairs, spine armature similar to males; superior tarsal claws—1st pair, slightly curved, 14 close teeth, increasing a little in length; inferior claw long, 2 teeth.

Palpi resemble legs in colour and armature; length 4mm. Palpal claw moderately curved, long, 7 teeth.

Falces yellowish, glossy; vertical, conical, tumid and projecting forwards at base.

Maxillæ rather longer than broad, apex wide, slightly rounded; yellowish. Labium less than one-half length of maxillæ, somewhat oval, broader than long, everted; olive-brown.

Sternum cordate; eminences opposite coxæ; yellow-brown, margin brownish.

Abdomen oviform, projects moderately over base of cephalothorax; light stone-colour; folium sinuate, olive-brown, stone-coloured flecks; on fore-third are a series of undulating angular marks—apices directed forwards, of a light stone-colour, except the largest and posterior one, which has a creamy-white hue, anterior margin reddish-pink; from the latter mark a narrow subulate light stone-coloured mark extends half-way to spinners; on dorsal line, intersecting the pattern, is an olive-brown streak, which takes a hastate form on the creamy angular bar; a series of brownish oblique broad

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streaks, interrupted by median pattern, extend length of folium; lateral margin yellowish-olive, white next to folium, flecks yellowish; on ventral surface is a semi-oval olive-brown mark, margined with light flecks; spinners short; light mahogany-brown. Vulva amber-colour, one - third broader than long, transversely rugose, projects over rima genitalis; displays two circular, moderately deep, brownish foveæ, divided by a slightly-elevated septum, whose breadth perceptibly exceeds their diameter, and nearly equals width of outer margin; facing septum is a somewhat concave depression, equalling it in breadth; margins of corpus vulvæ terminate, on either side of concavity, in slight, somewhat conical, brown eminences.

Several examples, summit of Te Aroha, A. T. U.

Linyphia nemoralis, sp. nov.

Female.—Ceph. th., long, 1. Abd., long, 1·5. Legs, 1, 2, 4, 3 = 7·4, 4, 3, 2·5 mm.

Cephalothorax dark olive-brown, suffused with black-brown; rugose; ovate lateral marginal compression at pars cephalica very slight; caput convex, viewed from front broad ovate; indentation below eyes; thoracic fovea longitudinal, normal grooves slight; profile-contour nearly semicircular, crown of arch at limit of caput; clypeus convex, projects moderately forwards, height equals about two-thirds depth of ocular area.

Eyes of tolerable and nearly equal size; posterior row procurved, median-pair three-fourths their diameter from each other, separated by scarcely twice that interval from side-eyes; anterior row recurved; centrals dark, smallest of eight, seated on a prominence, their radius apart, further from laterals of same row than they are from posterior median pair; form a trapezoid with hind-centrals, longer than broad; lateral eyes have the pearl-grey lustre of posterior-centrals, placed obliquely on dark, moderately prominent eminences, contiguous.

Legs brownish-yellow, rather faint-brown annulations, most pronounced on 3–4; in some examples, except base of femora, 1–2 have a reddish tinge, with little or no trace of annuli; slender; fine hairs, few bristle-like spines on genual and tibial joints.

Palpi straw-colour, except digital joint which has a brownish hue; latter article rather longer than humeral, more than twice length of pars radialis; no claw; black hairs.

Falces brownish-yellow, basal half suffused with reddish-brown; stout, length exceeds digital joint of palpus by one-fourth, project forwards at base, directed outwards, superior margin somewhat concave at extremity; outer row of teeth strong, two central longest; fangs long.

Maxillæ yellowish, basal half suffused with chocolate-brown;

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linear-oval, curve over labium, which is somewhat oval, rather broader than long, everted, more than half length of maxillæ; chocolate-brown, apex pale.

Sternum dark chocolate-brown; covered with small papillæ; cordate, nearly as broad as long.

Abdomen oviform, profile-line represents a semicircle, rising abruptly from base of cephalothorax; stone-colour; folium terminates a little above spinners, its dark-brown, coarse, irregular, somewhat acute-crenate margins enclose a stone-coloured leaf-like space, which has in some examples two angular brown bars on posterior half, apices directed forwards; fore-part of pale area and margins of folium widen out on base; ventral surface brown, margin dark. Corpus vulvæ moderately tumid, inferior (anterior) margin prolonged into a short, broad scape, fore-end circular, concave on upper side; superior margin curves inwards, forming a short septum, beneath the scapus vulvæ, which intersects two ovate foveæ; beneath the superior tumid margin is a narrow, transverse, lip-like projection.

Male.—Ceph. th., long, 1. Abd., long, 1. Legs, 1, 2, 4, 3 = 8, 5, 3·5, 3 mm.

Cephalothorax mahogany-brown; rugose; oval, lateral marginal constrictions at caput slight, contour of profile resembles female's; height of clypeus rather less than one-half depth of facial space.

Eyes, posterior row procurved, central pair their radius apart, rather more than their diameter from laterals; anterior row recurved, median pair placed on a dark, moderate prominence, separated by an interval equal to one-third of an eye's diameter, scarcely their breadth and a half from posterior-centrals, visibly more than their diameter from side-eyes of same row; laterals seated obliquely on moderate tubercular eminences, nearly contiguous.

Legs reddish-brown, except basal half of femora and coxæ, which have a dull straw-colour; 3–4 brown annuli at articulations of tibiæ and fore-end of metatarsi; armature, sparse, fine hairs; one long bristle-like spine on genual, two on tibial joints.

Palpi pale straw-colour; humeral joint about one-fourth longer than cubital and radial together; cubital joint rather narrow at base, slightly exceeds penultimate article in length; latter joint cyathiform, furnished with black bristles; pars digitalis reddish-brown; large, globose; laminæ moderately hairy, directed towards each other, circular, convex, project in front, a dark, stout, curved process, directed forwards and downwards; laminæ indented beneath processes, display above, on outer side, a remarkable lunulate indentation; bulbus genitalis complex, viewed laterally, circular, somewhat

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what (plane) spiral, rugose; margin black-brown, bulbus yellowish, circular margins reddish-brown; near centre of the somewhat depressed lobe are two yellowish, short, tooth-like processes, directed downwards; beneath them the dark, membranous margin is produced into a long, fine, black apophysis, curving forwards and upwards, central third ciliate.

Falces reddish-brown, basal half suffused with olive-brown, somewhat conical, directed visibly forwards, terminal half outwards.

Maxillæ brownish-yellow, base suffused with olive-brown; linear-oval curve over labium; latter oval, chocolate-brown.

Sternum dark chocolate-brown; cordate.

Abdomen oviform; stone-colour; folium nearly length of dorsal line; black-brown, coarse, acute - crenate margins enclose a stone-coloured leaf-like space. Ventral surface brownish.

Three specimens taken on the summit of Te Aroha, A. T. U.

Genus Theridium, Walck.

Theridium brunnea-folium, sp. nov.

Female.—Ceph. th., long, 2; broad, 1·2. Abd., long, 3; broad, 2·5. Legs, 1, 4, 2, 3 = 10·5, 8, 6·5, 5 mm.

Cephalothorax pale-brown, whitish radial streaks; caput, broad median band, and lateral margins suffused with brown; areolate; glabrous; oval, moderately compressed forwards, pars cephalica rather depressed, lateral index about equal to space at hind-central eyes; fovea large, deep, somewhat circular; radial striæ and caput-grooves moderately defined; contour of profile arched, dips slightly at median indentation; clypeus projects forwards, height visibly exceeds depth of ocular area.

Posterior row of eyes procurved; median pair—which are sensibly the largest of eight—separated by rather more than their diameter; interval between them and laterals exceeds latter space by one-third; anterior row recurved; central eyes slightly further from one another than they are from posterior median pair, with which they nearly form a square, anterior side widest; centrals rather less than their breadth from side-eyes; laterals placed obliquely on dark tubercular eminences, nearly contiguous.

Legs brownish-yellow, reddish-brown annulations on tibial and metatarsal joints; armature sparse, dark hairs, slender bristles.

Palpi yellowish, radial and digital joints reddish; length of cephalothorax.

Falces glossy, amber-colour; somewhat linear, directed slightly forwards, equal to pars digitalis of palpus in length.

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Maxillæ yellowish; long, somewhat acutely pointed, inclined over labium, which has an olive tinge; somewhat semicircular, nearly as long as broad, about one-half length of maxillæ.

Sternum yellowish, dark margins; cordate; areolate; slight eminences opposite coxæ.

Abdomen oviform, peduncle rather exposed; folium covers dorsal surface, runcinate, well-defined; light chocolates-brown, pale flecks, margins picked out with dark-brown; median band creamy-white; narrow, throws off few short transverse bars, fore-third lanceolate; lateral margins and ventral surface creamy-brown, numerous pale flecks; few brownish, transverse, somewhat ill-defined bars beneath; spinners short, brown. Vulva dark-brown; projects over rima genitalis, somewhat oval concavity above, fore-margin of latter tumid, notched.

Single specimen, summit of Te Aroha, A. T. U.

Theridium niger-punctillum, sp. nov.

Female.—Ceph. th., long, 2; broad, 1·5. Abd., long, 3; broad, 2·7. Legs, 1, 4, 2, 3 = 11, 8·2, 6·8, 4·8 mm.

Cephalothorax pale reddish-brown, caput and median band lightly clouded with olive; areolate; oval, laterally constricted forwards; pars cephalica moderately convex, lateral index equal to space from a hind-lateral eye to hind-central next to it; thoracic fovea circular, deep; normal grooves rather faint; profile-contour rises a little from occiput, represents a low arch across pars thoracica; clypeus directed perceptibly forwards, height equal to depth of eye-area.

Eyes tolerably small, do not differ much in size; posterior row procurved, median pair largest of eight, sensibly less than their diameter from each other, rather more than that space from side-eyes; anterior row recurved, centrals further from one another than they are from hind pair, with which they nearly form a square; lateral eyes have the pearl-grey lustre of posterior-centrals, placed obliquely on dark, moderately prominent, tubercular eminences, contiguous.

Legs yellowish, red-brown annulations at articulation of joints; femora of one pair speckled; long, slender; hairs and bristles sparse.

Palpi yellowish, hairs sparse, bristle on cubital joint; length, 2mm.

Falces yellowish, reddish about apex; linear, vertical.

Maxillæ pale, dull, brownish-yellow; stout, spathulate, inclined towards labium, which is semicircular, less than half length of maxillæ; slightly everted; orange-brown.

Sternum colour of legs; areolate; cordate.

Abdomen oviform, very convex above, pointed at spinners, moderately so at base; pale, olive-tinted stone-colour, thickly

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spotted with creamy-white flecks, oblique streaks of normal hue, remarkable irregular black mark between second and last oblique streaks; hairs short, light, sparse. Vulva glossy, reddish-black; represents two somewhat circular connected projections; on upper surface are two foveæ, intersected by a longitudinal groove; reddish-brown fan-shaped marks radiate from each concavity.

Single specimen captured at the base of Te Aroha, A. T. U.

Theridium porphyreticum, sp. nov.

Female.—Ceph. th., long, 2; broad, 1·5. Abd., long, 3; broad, 2. Legs, 1, 2, 4, 3 = 9, 6, 5·4, 4 mm.

Cephalothorax pale, brownish straw-colour; areolate; oval, slightly compressed forwards; pars cephalica moderately convex; lateral index equal to space from a fore-lateral eye to the hind-central next to it; thoracic fovea somewhat oval, normal grooves deep; contour of profile represents a moderate arch; clypeus nearly vertical, height scarcely equals depth of eye-area.

Posterior row of eyes sensibly procurved, median pair ovate, pearl-grey, black margins, separated by an interval perceptibly exceeding their breadth, their diameter and a half from laterals next to them; anterior row recurved, centrals brownish, placed on moderate black eminences, nearly form a square with posterior pair; lateral eyes have the brownish hue of fore-centrals, seated obliquely on black tubercular eminences, contiguous.

Legs and cephalothorax concolorous; moderately slender; armature very sparse.

Palpi colour and armature of legs.

Falces brownish straw-colour; vertical, somewhat linear and aplanate, double row of small teeth.

Maxillæ long, ronndly truncated on superior side, single row of short bristles on margins, inclined towards labium, which is about as long as broad, rounded; organs pale-brown.

Sternum yellowish, cordate.

Abdomen oviform, basal end rather the widest and most pointed; dorsal field—except base, which is light-brown—clouded with black-brown, has a pinkish tint graduating into a pale yellow-brown, thickly flecked with a lighter hue, about marginal zone and ventral surface; posterior three-fourths of dorsal field clouded with reddish-purple, deepening in shades towards spinners; on median line are two creamy-white marks; basal lanceolate, forms a disconnected petiole to the doubly serrate leaf-shaped posterior mark, which extends to spinners; across the constriction, below the central im-

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pressed spots, is a dash of red. The abdomen in the vicinity of the vulva had shrunk somewhat when the specimen was described. Branchial opercula long, linear; pale-lemon colour. Corpus vulvæ moderately prominent; above the rima genitalis is a large circular orifice.

Single example, Wairongomai Gorge, A. T. U.

Theridium gracilipes, sp. nov.

Female.—Ceph. th., long, 1·1; broad, 1. Abd., long, 2; broad, 1·6. Legs, 1, 4, 2, 3 = 11·5, 7·5, 7·3, 6 mm.

Cephalothorax light-brown clouded with olive-brown, except fore-part of pars cephalica and lanceolate median streak; areolate; ovate, base broad; caput moderately convex, roundly truncated; eminence of fore-central eyes projects a little forwards; thoracic indentation somewhat triangular, normal grooves fairly defined; contour of profile represents a low arch; clypeus directed forwards, height nearly equals depth of ocular area.

Fore and hind row of eyes recurved, curvature of posterior row nearly equals that of anterior; eyes of hind row of equal size, centrals are separated from one another by an interval equal to their diameter, and from laterals by about their radius; anterior-centrals dark, seated on a moderate blackish prominence, less than their diameter apart, about one-third smaller than hind-median pair, with which they form a trapezoid, whose posterior side is widest; lateral eyes have the pearly lustre of posterior-centrals, placed obliquely on strong, dark-lake rings, nearly contiguous.

Legs yellow-brown; short, stiff hairs, apparently no bristles; long, slender.

Palpi resemble legs in colour; dark hairs, fine bristle on cubital and radial joints; slender.

Falces yellowish; vertical, somewhat conical, fore-third directed outwards.

Maxillæ yellowish-brown; spathulate, inclined towards labium, which is semicircular, margins very tumid; yellowish-brown, base dark.

Sternum yellow-brown, margins olive-brown; cordate, numerous small mammiform eminences.

Abdomen, profile oviform, posterior end obtuse, viewed from above pointed somewhat sharply at either extremity; integument olive-brown, posterior end dark, on dorsal field and lateral margins are about 15 irregularly-shaped light stone-coloured patches; ventral surface olive-brown; hairs short, sparse. Corpus vulvæ moderately prominent, dark amber-colour; within a rather large circular area, defined by a narrow membrane, are three moderately prominent lobes enclosing a cordate space, apex directed towards spinners,

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rather exceeding the upper and largest lobe in size; lateral lobes mussel-shaped, superior reniform.

Single specimen, colour affected by spirit. Te Aroha, A. T. U.

Fam. Epeiridæ.

Genus Epeira, Walck.

Epeira dumicola, sp. nov.

Female.—Ceph. th., long, 2·5; broad, 2·2; facial index, 1. Abd., long, 5·2; broad, 4·2. Legs, 1, 2, 4, 3 = 8·7, 8·1, 7·5, 4·5 mm.

Cephalothorax dull raw-sienna; few pale hairs on pars thoracica; clathrate; length equals that of the genual and tibial joints of a leg of 4th pair; sides well-rounded, lateral constrictions at caput tolerably sharp; pars cephalica convex, ocular eminence rather low, lateral index equals space between posterior-lateral eyes; thoracic indentation and radial striæ not well-defined, caput-grooves more pronounced; profile-contour rises from thoracic junction at an angle of 30°, slopes forwards across three-fourths of caput; clypeus nearly equals diameter of a fore-central eye in depth.

Posterior row of eyes sensibly procurved, median pair separated by an interval which perceptibly exceeds their diameter; their space and a quarter from side-eyes; anterior row moderately recurved, centrals visibly smaller than posterior pair, have their lake-brown tinge and rings, interspace equal to about twice their diameter, rather less than that interval from hind-median eyes; about twice their space from side-eyes; laterals nearly equal hind-centrals in size, seated obliquely, visibly more than their radius from each other, on separate lake-brown tubercular eminences.

Legs moderately slender; reddish-chestnut colour; faint annuli; hairs light, sparse; spines slight, yellowish, moderately numerous; superior tarsal claws—1st pair, 10 teeth; inferior claw, 2 short close teeth.

Palpi and legs concolorous; slender, equal to cephalothorax in length; armature slight spines and hairs; palpal claw, curvature moderate, 8 teeth directed forwards.

Falces yellowish, apices and fangs dark; conical, vertical, project at base in front; length equal to breadth of anterior row of eyes.

Maxillæ strong, obtusely pointed, inclined towards labium: latter oval, about as broad as maxillæ, three-fourths their length; organs, base red-chestnut, apices yellowish.

Sternum colour of coxæ; shield-shape; clathrate.

Abdomen projects over base of cephalothorax; broadest between moderately pronounced tubercles, base obtusely pointed, tapers towards spinners; aplanate; hairs fine,

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sparse; ground-colour creamy-brown; a moderately angular brown mark intersects anterior pair of impressed spots, which are in line with tubercles at its apex, which is directed forwards, is an oval yellowish spot, with orange-red margins; between central pair of impressed spots, which are also well defined, is a brown Y-shaped mark; few faint angular bars towards spinners. Vulva yellowish; convex, transversely rugulose; scapus large, somewhat conical, about as broad at base as long, lateral margins of basal half membranous, red-chestnut colour, prolonged margins curve inwards, forming somewhat triangular concavities beneath scapus vulvæ.

Single example, captured on summit of Te Aroha, A. T. U.

Epeira mulleola, sp. nov.

Male.—Ceph. th., long, 4·5; broad, 3·8. Abd., long, 4·5; broad, 3. Legs, 1, 2, 4, 3 = 15·5, 13·5, 12·4, 8·5 mm.

Cephalothorax, sides olive-brown, graduating to a reddish-brown on median line; moderately clothed with white hairs; sides well-rounded, laterally compressed forwards; pars cephalica somewhat depressed, shallow central indentation; lateral index slightly exceeds one-half facial index; ocular eminence prominent; pars thoracica moderately convex, indentation large, somewhat circular.

Posterior-central eyes separated from each other by a space equal to their diameter and a half; their breadth from fore-centrals; anterior median eyes perceptibly the largest, interval between them equals their diameter and a half; laterals seated on moderately strong, black, tubercular eminences, their radius apart; fore-pair visibly the largest.

Legs light-brown, tinted—especially 1–2—with light olive-green, fore-part of femora clouded with dark olive-brown; tibial, metatarsal, and tarsal joints annulated with olive-brown, less defined on tibiæ of 1–2; genual joints rather more than half length of tibial; latter articles equal metatarsal in length; tibia of a leg of 1st pair equal to cephalothorax in length; curved process on coxæ of 1; hairs yellowish, short, tolerably sparse; spines yellowish, base dark; several long spines on femora of 1–2; 3–4, superior and inferior row of about 4 or 5 spines, mostly exceeding former in length and strength; spines on genual joints; fairly numerous and strong on tibiæ, especially of 1–2; 10 to 15 spines on metatarsal joints; superior tarsal claws—1st pair, 11 open comb teeth; inferior claw sharply bent, 2 close teeth.

Palpi, hairs pale-yellow; humeral joint yellow - brown; short, fore-end somewhat dilated, furnished with a long, stout bristle; cubital joint yellowish; broad cordate, base constricted, more than half length of pars humeralis, projects at apex a long, strong, yellowish-brown bristle; radial joint

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tinted with olive-brown; one-third length of former article, produced on outer side into a large, pale straw-coloured, oval process, directed outwards and slightly downwards; pars digitalis large, oval; laminæ bulbi yellowish, clouded with olive-brown; ovate, apices curved; directed towards each other; base prolonged on outer side into a reddish curved process, directed outwards; bulbus genitalis complex; crown light reddish-brown, clouded; somewhat oval, convex, horizontally rugose, on summit is a dark-reddish circular bead; bulb displays several curved, obtusely-pointed convolutions, yellowish-brown, blackish-red margins; most remarkable projections—view laterally, fore-lobe somewhat vertical in front, upper margin developed into a bright red-mahogany, semi-detached, broad, cylindrical, horizontal process, curving backwards, about its diameter below upper disc; projecting downwards from margin of disc is a large, bright mahogany-red, flattish, somewhat cordate lobe, apex curved forwards, in contact with apex of cylindrical process; between cordate lobe and a semipellucid black-marked membrane at articulation of bulb is a broad, blackish, longitudinally-wrinkled appendage, fore-end concave, hind limb claw-like, directed backwards; beneath cordate lobe is a large, brownish-lake, curved process, projecting outwards and somewhat forwards, nearly as broad as long, concave above, apex truncated, somewhat U-shaped.

Falces yellow-brown, basal two-thirds yellow, streaked with olive-green; vertical, moderately slender, outer contour concave, inner convex, fore-third directed outwards; fangs lake-colour.

Maxillæ, fore-end dilated, rather broader than lip, obtusely pointed, inclined towards each other. Labium rather broader than long, lateral margins abrupt, slope perceptibly outwards, obtusely pointed, everted; organs, base dark-brown, fore-end pale olive-brown.

Sternum blackish-brown; white hairs; ovate, transversely rugose.

Abdomen oviform, moderately prominent across greatest diameter; posterior end rounded, two well-developed tubercles, one above the other, lower perceptibly the largest; eight impressed spots; anterior pair of four central, well defined, placed at case of transverse ridge; ground-colour light slaty stone-colour; folium trilobate, margins black-brown, resembles females in form and marks; lateral margins tabby-grey; ventral surface brownish-yellow, shield blackish.

Female described in vol. xx. “Trans. N.Z. Inst.”* This species is by no means rare, commences pairing in October: cocoon globose, composed of dark-green silk, of loose texture;

[Footnote] *“Trans. N.Z. Inst.,” vol. xx., p. 118, and pl. xi., fig. 6.

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comprised within are about 360 pinkish eggs, agglutinated together.

Tairoa, T. Brown; Te Karaka, A. T. U.

Fam. Thlaosomidæ.

Genus Thlaosoma, Cambr.

Thlaosoma tuberosa, sp. nov.

Female.—Ceph. th., long, 2; broad, 2·7. Abd., long, 3·1; broad, 5. Legs, 1, 2, 4, 3 = 8·2, 8, 6, 5 mm.

Cephalothorx pale stone-colour, olive-tinge, base and lateral margins semi-pellucid, striæ defined by interruped dark-brown streaks; pars cephalica brownish, light olive-brown oblique bars; median streak yellowish-brown, acute; eye-area reddish, cross yellow; hairs papillæform, white and reddish; pars thoracica somewhat reniform, raised into two abrupt ridges, terminating in prominent sub-conical points above thoracic junction; fore-part of pars cephalica somewhat conical, has the normal upturn; height of clypeus nearly equals depth of ocular area.

Four central eyes form a quadrilateral figure broader than long, of about equal size; laterals rather smaller than median eyes, their radius apart.

Legs brownish-yellow, broad, somewhat flecked, brown annuli on femora; two broad annulations on tibiæ; single one at fore-end of metatarsi; 1–2 and 3–4 of about equal strength, two fore-pairs stoutest; femoral joints armed beneath with double row of moderately short and strong tubercular spines, numerous smaller spines between rows; similar rows, composed of smaller spines, beneath tibiæ of 1–2; hairs sparse; outer superior tarsal claw—1st pair, much the longest and strongest, 4 close teeth; inner claw 5; inferior claw sharply bent, 2 short teeth.

Palpi and legs concolorous; palpal claw sharply curved, 3 teeth increasing in length and strength.

Falces clouded with blackish-olive, fangs red; long, somewhat linear, directed inwards.

Maxillæ rather longer than broad, roundly pointed, inclined over labium, which is large, broader than long, somewhat pointed; organs chocolate-brown, apices light.

Sternum olive-brown, clouded with dark-brown; cordate.

Abdomen, base and lateral margins have a pinkish tint; in centre of concave depression above thoracic junction is a linear-oval, red-brown mark; dorsal surface, except posterior third, which represents a creamy-white triangular area, is black-brown; tubercular eminences mostly yellowish-brown; hairs papillæform, numerous, reddish and white; the apices of the two lateral and leading protuberances are nipple-like;

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these protuberances are shorter and more sharply constricted than in T. olivacea; on the darker portions are numerous fair-sized rounded humps; spinners stout, dark. Corpus vulvæ pale stone-colour, somewhat triangular, about twice as long as broad, centrally produced above the rima genitalis into a brownish lip, about as broad as long, concave above.

Fam. Attidæ.

Genus Plexippus, C. Koch.

Plexippus herbigradus, sp. nov.

Male.—Ceph. th., long, 4; broad, 2·5. Abd., long, 4; broad, 2·1. Legs, 1, 4, 2, 3 = 8, 6·3, 5·6, 5·5 mm.

Cephalothorax, caput brownish, more or less suffused with bright orange-red, mottled with a creamy-brown penetrative tint; two dark spots in line with second row of eyes; thorax reddish-mahogany colour; few pale hairs, sparse yellowish fringe on frontal margin; broad oval, pars thoracica slightly exceeds pars cephalica in length, latter aplanate, limited by a somewhat diamond-shaped indentation; profile-contour rises at an angle of 45°, slopes perceptibly across caput; clypeus vertical, equal in height to radius of a fore-lateral eye.

Anterior row of eyes slightly recurved; laterals separated from central pair by nearly their diameter, latter pair rather less than that interval from each other; interspace between posterior eyes, which are visibly larger than anterior-laterals, perceptibly exceeds space dividing latter pair; eye-area about one-fourth broader than long; angles somewhat prominent, black-brown.

Legs brownish-yellow, genual and tibial joints of 1st pair reddish-mahogany, penultimate and terminal joints darkish-brown; 1st pair stoutest; genua and tibia together equal cephalothorax in length; tibial joint one-third longer than genual; metatarsal and tarsal joints thinner than tibial, one-fourth longer than that article; 2 slightly exceed 3–4 in strength, latter of about equal stoutness; hair light, sparse; about 5 spines on femora of 1–2; 6 or 7 on femora of 3–4; spine on inner side of genual joints of 1; tibiæ and metatarsi of 1–2,—3–3, 2–2; tibiæ of 3–4 have 4 spines; metatarsi 2, with rings of 5; outer claw, one strong tooth near bend of claw; inner, about 10 short close teeth; claws well curved, claw-tuft long.

Palpi, humeral and cubital joints resemble legs in colour; former article equals three terminal joints in length; pars cubitalis somewhat linear, rather stouter than humeral joint; pars radialis darker, slimmer, and about one-half length of

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pars cubitalis, projects on outer side a stoutish process, apex fine, curved upwards; lamina bulbi mahogany-colour, moderately hairy; rather longer than two former articles together, apex obliquely truncated, slope directed outwards, somewhat depressed; bulbus genitalis chocolàte-brown, nearly two-thirds length of lamina; viewed beneath, from inner side, somewhat triangular; projecting from apex are two moderately-long, fine, curved apophyses, inner black, outer pellucid; beneath lamina, on outer side, is a yellowish tumid bulb, whose free end extends backwards to radial joint.

Falces purple-chocolate; conical, vertical, transversely rugose; length equal to posterior breadth of ocular area.

Maxillæ red-mahogany colour; fore-end broad, rounded.

Labitim linear-oval; colour of maxillæ.

Sternum reddish-brown; oval.

Abdomen linear-oviform; olive-tinted stone-colour, numerous light flecks on lateral margins and dorsal line; folium brownish, coarsely serrate, encloses a linear-oval, light olive-green mark, with few brown spots; series of three oblique brown streaks on lateral margins; ventral surface brownish; hairs sparse.

Female.—Ceph. th., long, 3; broad, 2. Abd., long, 4; broad, 2. Legs, 1st pair, 5mm.

Cephalothorax yellowish - mahogany, caput mottled with creamy-brown, fore-half clouded with a darkish-brown; few hairs on margin of eye-area; pars cephalica aplanate, sides moderately abrupt, limited by a somewhat diamond-shaped depression, scarcely equals length of pars thoracica; profile-line rises from thoracic junction at an angle of 45°, dips slightly forwards across caput; clypeus vertical, equals radius of a fore-lateral eye in depth; fringe of light hairs.

Angles of eye-area less prominent than males.

Legs brownish-yellow, anterior pair shade darker, especially four terminal joints; genual and tibial joints of 1 more than three-fourths length of cephalothorax; hairs sparse; few spines on femora; single spine on inner side of genua of 1; tibiæ of 1–2, as a rule, 3–4; metatarsi, 2–2; tibiæ of 3–4, about 4 or 5; metatarsi 2, rings of 5 spines.

Palpi and hind-legs concolorous; sparsely furnished with hairs; slender; length, 2·4mm.

Falces reddish-mahogany; broad conical, less pointed and shorter than males, vertical, transversely rugose.

Maxillæ brown; extremity broad, rounded. Labium brown; linear-oval, about half length of maxillæ.

Sternum oval; yellowish.

Abdomen linear-oviform; ground-colour deep stone-colour, numerous pale flecks; folium coarsely serrate, olive-brown, encloses a pale, mottled, lanceolate figure, with serrate mar-

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gins, and about five dark spots; on lateral margins are a series of three oblique darkish streaks, converging towards spinners; ventral shield linear-ovate; normal dark hue. Abdomen sparsely clothed with hairs. Vulva red-mahogany; moderately prominent; displays above, two circular foveæ, divided by a longitudinal septum, whose breadth about equals their diameter; on the tumid margin, above the rima genitalis, are two bright reddish-mahogany circular convexities, connected by a broad ligament, whose breadth equals their diameter.

Examples of this species were captured on the summit of Te Aroha; were numerous—especially males—amongst the ferns up the Wairongomai Gorge. Individually they varied both in coloration and distinctness of pattern. A. T. U.

Art. XIII.—On a new Species of Gasteracantha, from Norfolk Island.

[Read before the Auckland Institute, 22nd October, 1888.]

Plate VII.
Fam. Epeiridæ.

Genus Gasteracantha, Sund.

Gasteracantha ocillatum, sp. nov. Plate VII., figs. 1–3.

Female.—Ceph. th., long, 3·2; broad, 2. Abd., long, 6·5; broad, 16; to apex of posterior spines, 21·5. Legs, 4, 1–2, 3 = 10, 9, 7 mm.

Cephalothorax brown, clouded, more especially on caput and sides, with black; hairs sparse, short, yellowish; broad oval, slightly compressed forwards, pars cephalica squarely truncated, frontal contour between ocular eminence, which is low, and fore-lateral eyes perceptibly convex; caput limited by a rather deep transverse groove, which takes a procurved lunulate form on median line; base rises, somewhat abruptly, into two sub-conical prominences, divided by a longitudinal cleft nearly equal to base of prominences in width, connected with ocular eminence by two rather faint lateral striæ; pars thoracica somewhat depressed, radial striæ well defined; profile-contour of pars cephalica conical, slight slope across thorax; height of clypeus visibly exceeds diameter of an anterior central eye.

Four median, eyes represent a trapezoid, whose anterior side is shortest; posterior pair sensibly the largest, more than twice their space from side-eyes of same row, separated from each other by rather more than twice their diameter,

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scarcely that interval from anterior pair, which are visibly more than an eye's breadth and a half from one another; lateral eye's perceptibly smaller than centrals, seated obliquely, their radius apart, on a stout tubercular eminence.

Legs reddish - mahogany colour (brown - mahogany in second example); hairs black, few fine bristles; 1–2 of nearly equal length and strength; 4 exceeds 3 in length and somewhat in stoutness; superior tarsal claws—1st pair, moderately curved (apparently), 8 rather strong, open teeth; inferior claw long, bent, teeth (?); auxiliary claws.

Palpi tolerably slender, colour and armature of legs; palpal claw slightly curved, 7 open teeth, centrals longest.

Falces dull-black, lake tinge; stout, somewhat pyriform, directed moderately forwards, nearly equal, in length radial and digital joints of palpus; double row of strong teeth, outer row 7.

Maxillæ stout, about as broad as long, somewhat semicircular, base constricted, slightly inclined towards labium, which is about as long as broad, somewhat conical, everted, rather more than one-half length of maxillæ; base of organs chocolate-brown, margins olive tinted yellow-brown.

Sternum elongate-cordate, well-defined eminences oppoisite coxæ, base tapers off to a tail-like point from posterior pair; brownish-black; large, circular, brownish-yellow spot between anterior pair of eminences.

Abdomen light-yellowish stone-colour, area enclosed by sigilla, from first pair slightly suffused with a dull olivegreen (less defined in second example); fore and hind margins have a pale-olive hue, sparsely clouded with streaks of lake; lateral extremities, fore-spine, and base of hind-spine, black; fore-part of latter spine red-lake, apex dark; posterior spine-like tubercles lake-black; sigilla black, tinted more or less with brown-lake; centre and extremities of ventral surface greenish-black, intermediate longitudinal bands, which equal central in breadth, have a yellowish hue, suffused with lake; irregularly-shaped yellowish-coloured spots, base of two largest partially encircle spinners, tapering off round posterior margins of branchial opercula; few short black hairs on margins and posterior tubercles; horny; rather more than twice as broad as long, aplanate, lateral wing-like projections rise to an angle of 25°, terminate with stout spines directed outwards; anterior pair 1mm. in length, inclined slightly forwards; posterior pair, 4mm., curve moderately backwards; viewed from above, profile-contour of central third represents a visibly-depressed segment of a circle projecting over base of cephalothorax; extremities of line slope perceptibly backwards to anterior spines; from apex of posterior spines to base of tubercles profile-line forms a slight and even concavity; tuber-

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cles, 2mm. long, directed backwards and visibly outwards; on dorsal margins are a series of sigilla, ten in each row (in one specimen eleven are represented in anterior row, the second outer sigillum on left side having a double form, probably abnormal); anterior row—central pair circular, smallest of series; outer sigillum large, ovate; between latter and inner sigillum are intermediate forms decreasing in size; in posterior row outer pairs of sigilla are smaller and of a linear-oval form; in centre of abdomen are four small linear-oval sigilla representing a trapezoid, whose posterior side is widest; from the tumid posterior margin abdomen dips abruptly, 4mm., to spinners; this area has, including the marginal, five well-developed transverse corrugations, first connects base of posterior lateral spines, second projects backwards, and bears the spine-like tubercles; three corrugations on ventral surface; in all grooves are small sigilla, ten in first row; at extremity of each wing-like projection is a large, blackish, ovate sigillum, equal to dorsal one in size. Vulva black; large, somewhat conical, apex rounded; viewed from posterior end displays a membranous ridge, terminating beyond base.

This species is closely allied to Gasteracantha westringii, from New Holland, described and figured by Koch in “Die Arachniden Australiens.” Two examples were captured by Miss Lodge at Norfolk Island. I am indebted to Mr. T. F. Cheeseman, F.L.S., for the specimens which he handed over to me for determination.

Description of Plate VII.

Gasteracantha ocillatum.

Fig. 1. Female.

Fig. 2. Maxillæ, lip, and sternum.

Fig. 3. Posterior view.

Art. XIV.—Descriptions of New Zealand Micro-Lepidoptera.

[Read before the Philosophical Institute of Canterbury, 1st Nov., 1888.]

The following descriptions include all the material remaining undescribed in my hands of these groups. It is for resident collectors to obtain fresh material and information on the habits of described species, and I shall at all times welcome any communication from those who have the opportunity of doing so, and will gladly determine any species sent to me.

Picture icon

Gasteracantha Ocellatum.

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Botydidæ.
Mnesictena, Meyr.

1. Mnes. daiclealis, Walk.

(Scopula daiclesalis (rect. daiclealis), Walk., 1017.)

[The section below cannot be correctly rendered as it contains complex formatting. See the image of the page for a more accurate rendering.]

♂. 22mm. Head and thorax deep ferruginous. Palpi 4, deep ferruginous, sprinkled with dark grey; base white beneath. Antennæ pale ochreous. Abdomen light ochreous-yellowish. Legs pale ochreous, anterior tarsi and middle tibiæ white. Forewings triangular, costa slightly sinuate in middle, strongly arched on posterior half, apex tolerably rectangular, hindmargin rather bowed, oblique; ferruginous-brown, irrorated with dark grey; inner margin rather broadly suffused with ochreous-orange from base to ¾; a narrow ochreous-orange streak along costa from base to ¾, enclosing a very slender snow-white costal streak from ¼ to ⅔; lines thick, cloudy, dark grey, very indistinctly defined; first about ¼, oblique, not reaching either margin; second from 2/4 of costa to ⅔ of inner margin, upper ⅔ moderately curved outwards; reniform obscurely outlined with dark grey, very indistinct: cilia ferruginous-brown suffused with grey. Hindwings light ochreous-yellowish; a dark-grey dot in centre of disc; partial indications of a slender, greyish line at ⅔; cilia pale whitish-yellowish, reddish-tinged.

“Wellington and Dunedin. I am indebted, for the opportunity of describing this species to the liberality of Mr. G. V. Hudson, who states that it is attracted by fight, and is scarce.

Scopariadæ.
Scoparia, Hw.

2. Scop. hemiplaca, n. sp.

♂. 18mm. Head, palpi, antennæ, and thorax dark fuscous; palpi 2¼, base white beneath; antennal ciliations ⅓. Abdomen light grey, and tuft whitish-ochreous. Legs dark fuscous, apex of joints and posterior tibiæ whitish. Forewings elongate, moderately dilated posteriorly, costa slightly arched, apex obtuse, hindmargin almost straight, rather oblique, rounded beneath; dark fuscous, with purplish reflections; first, line obscurely indicated on lower half only, slightly paler than ground-colour; a suboblong white blotch, sprinkled with fuscous, extending along inner margin from middle to hindmargin, reaching half across wing, its upper anterior angle rounded off, upper side shortly indented in middle; this blotch is sharply defined, and margined in front and above by a thick black suffusion, in which the lower half of reniform is indicated by an obscure spot of ground-colour;

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second line slightly paler than ground-colour, darker-margined, forming a whitish dot on costa, becoming obsolete on the white blotch, but its margins partially indicated by fuscous scales; an erect wedge-shaped white subapical spot; a white entire hindmarginal line: cilia ochreons-whitish, with an interrupted dark-grey line, and on upper half of hindmargin with obscure light-grey bars. Hindwings 1¼; pale grey; indications of a faint paler postmedian line; cilia ochreous-whitish, with an interrupted grey line.

Wellington; one specimen received from Mr. G. V. Hudson, who bred it from a larva feeding on moss. It is a conspicuously-distinct species, at once recognised by the peculiar white blotch; its nearest known ally is S. minusculalis.

Tortricidæ.
Cacœcia, Hb.

3. Cac. astrologana, n. sp.

♂. 16–22mm. Head, palpi, antennæ, thorax, abdomen, and legs pale whitish-ochreous; palpi long; anterior legs infuscated. Forewings elongate-triangular; costa strongly arched, apex obtuse, hindmargin slightly sinuate, somewhat oblique, costal fold short; whitish-ochreous, with a few fine scattered black scales; a small black dot in dise before middle, a second in disc at ⅔ (in Tasmanian specimen absent), a third beneath costa at ⅔, a fourth in disc at ⅚, and a fifth towards inner margin at ⅔: cilia pale whitish-ochreous. Hindwings whitish, with a few scattered light-grey speckles; cilia whitish.

Wellington; one specimen received from Mr. G. V. Hudson. I took a specimen also at Deloraine, Tasmania, in November; the species is very distinct, and I have no doubt of their identity.

Proselena, Meyr.

4. Pros. eribola, n. sp.

♂. 14–15mm. Head, palpi, and thorax dark reddish-ochreous-brown. Antennæ brownish-ochreous, ringed with dark fascous. Abdomen dark fuscous. Legs dark fuscous, apex of joints pale yellowish, posterior tibiæ pale greyish-ochreous. Forewings oblong, posteriorly scarcely dilated, costa on basal half rather strongly arched, then straight, apex obtuse, hindmargin slightly sinuate, somewhat oblique; dark reddish-ochreous-brown; a somewhat darker but very ill-defined central fascia from before middle of costa to inner margin before anal angle, narrow on costa, suddenly dilated above middle, thence to inner margin rather broad: cilia dark reddish-ochreous-brown, terminal half pale reddish-ochreous, on costa barred with dark brown. Hindwings and cilia dark

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fuscous; tips of cilia shortly below apex sometimes pale reddish-ochreous.

Otira River (3,000ft.), amongst forest, in January; four specimens. A distinct species, perhaps nearest P. zatrophana.

Glyphipterygidæ.
Heliostibes, Z.

5. Hel. electrica, n. sp.

♀. 16–17mm. Head, palpi, thorax, and abdomen dark fuscous, slightly sprinkled with yellowish. Antennæ and legs dark fuscous, posterior tibiæ yellow-whitish. Forewings elongate, moderate, costa gently arched, apex rounded, hind-margin obliquely rounded; dark fuscous, strewn with ochreous-yellow hair-scales in irregular patches; a leaden-metallic line from ⅓ of costa to ⅖ of inner margin, angulated outwards in middle; a sinuate leaden-metallic line from above middle of disc to anal angle; a leaden-metallic line from middle of costa-obliquely outwards more than half across wing, thence curved round to touch a whitish dot on costa at ¾, and continued in a strong curve near and parallel to costa and hindmargins to anal angle; space between first and second lines, and within first curve of third line, less strewn with yellow scales and therefore darker than rest of wing: cilia light grey, rather shining. Hindwings rather dark fuscous, somewhat bronzy; cilia light shining grey.

Mount Arthur (4,700ft.), in January; two specimens. Very distinct.

Plutellidæ.

Eutorna, n. g.

Head smooth, sidetufts projecting over forehead; ocelli absent; tongue well-developed. Antennæ ⅘, in male serrate, shortly ciliated (¼–⅓), basal joint moderately long, without pecten. Labial palpi long, curved, ascending, second joint thickened with dense appressed scales, terminal joint shorter than second, slender, acute. Maxillary palpi very short, drooping. Posterior tibiæ clothed with hairs above. Forewings with vein 1 furcate, 2 from very near angle, 6 to apex, 7 and 8 stalked, 11 from before middle. Hindwings almost or quite as broad as forewings, elongate-ovate or broadly lanceolate, cilia 1⅓; all veins separate, 5 bent.

Approaches most nearly to Compsistis, from which it differs mainly in the antennæ not being as long as forewings, and in veins 3 and 4 of the hindwings being separate. Besides the two following species I have several Australian, which are closely allied to them:—

Ground-colour of forewings ferruginous-brown caryochroa.
" " " ochreous symmorpha.
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6. Eut. caryochroa, n. sp.

♂ ♀. 11–12mm. Head ferruginous-brown, face whitish-ochreous. Palpi ochreous - white, apex of second joint ochreous, terminal joint almost as long as second, dark fuscous. Antennæ fuscous, ringed with black. Thorax ferruginous-brown, shoulders pale ochreous. Abdomen fuscous. Legs dark fuscous, ringed with ochreous-whitish. Forewings elongate, narrow, costa moderately arched, more strongly towards base, apex round-pointed, hindmargin extremely obliquely rounded; rather dark ferruginous-brown; an upwards-curved yellowish-white streak from middle of base to ⅖ of disc, margined beneath with blackish, above with bright yellow-ochreous, which extends to costa towards base; a slender white oblique streak from ⅖ of costa to middle of disc, margining a triangular costal suffused patch of purplish-grey and whitish scales, beneath which is sometimes a longitudinal blackish suffusion; a black dot in disc at ⅔, surrounded by a yellowish-white ring; some purplish-grey scales towards posterior half of inner margin; a small white spot on costa at ⅘, beyond which is a blackish suffusion; an obscure irregular whitish streak along hindmargin, followed by some black scales: cilia ochreous, towards anal angle greyish-tinged, round apex with a white median line preceded and followed by fuscous shades. Hindwings rather dark bronzy-fuscous; cilia fuscous-grey.

Castle Hill (2,500ft.), Dunedin, Lake Wakatipu, and Invercargill; in December and January, rather common.

7. Eut. symmorpha, n. sp.

♂ ♀. 12–14mm. Head and thorax yellow-ochreous, face whitish-ochreous, Palpi yellow-ochreous, terminal joint much shorter than second, whitish. Antennæ ochreous-whitish, ringed with pale fuscous, towards base ochreous. Abdomen whitish-ochreous. Legs whitish-ochreous, tarsi and anterior tibiæ more or less infuscated. Forewings elongate, narrow, costa moderately arched, more strongly near base, apex round-pointed, hindmargin extremely obliquely rounded; yellow-ochreous, sometimes obscurely streaked with whitish-ochreous between veins, veins more reddish-ochreous or brownish-ochreous; a straight, slender, reddish-brown streak from middle of base to disc at ⅖, terminating in a small blackish spot, cloudy beneath, above sharply-defined and sometimes margined with an ochreous-whitish streak; a more or less distinct reddish-brown streak from disc before middle to costa before apex, terminating in some black scales; two black dots transversely placed in disc at ⅔; some black scales on hindmargin: cilia pale ochreous, round apex with an ochreous-brown line. Hindwings and cilia light grey.

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Whangarei, Hamilton, Palmerston, Napier, Christchurch, Dunedin, and Invercargill; from December to March, common.

Hyponomeutidæ.

Archyala, n. g.

Head with loosely-appressed hairs; ocelli present; tongue developed. Antennæ ¾, in male serrate, pubescent, basal joint moderate, without pecten. Labial palpi moderately long, curved, ascending, second joint with rough projecting scales towards apex beneath and two or three apical bristles above, terminal joint shorter than second, somewhat loosely scaled, laterally compressed, obtuse. Maxillary palpi rather short, appressed to face. Posterior tibiæ clothed with long hairs above and beneath. Forewings with vein 1 furcate, 2 from angle of cell, 7 and 8 stalked, 7 to costa, 11 from middle. Hindwings 1, elongate-oblong, apex round-pointed, hind-margin very oblique, cilia 1; with an ill-defined hyaline patch towards base; veins 2, 3, 4 remote and parallel, 5 and 6 stalked, 6 to close below apex, 7 approximated to 6 at base.

Nearly allied to Lysiphragama, but separable by the stalking of veins 7 and 8 of forewings, absence of scaletufts on surface, and hyaline patch of hindwings.

8. Arch. paraglypta, n. sp.

♂ 16mm. Head fuscous-whitish, more fuscous between, antennas. Palpi dark fuscous, terminal joint whitish. Antennæ fuscous. Thorax fuscous, posteriorly mixed with whitish. Abdomen fuscous. Anterior legs dark fuscous ringed with whitish, middle legs ochreous-white banded with black, posterior legs ochreous-whitish banded with fuscous. Forewings very elongate, narrow, costa moderately arched, apex round-pointed, hindmargin extremely obliquely rounded; white, irregularly transversely strigulated with grey, and more or less suffused with pale brownish-ochreous except towards inner margin and base, and on costal edge; numerous irregular incomplete transverse dark fuscous strigulæ, tending to partially coalesce in pairs: cilia grey-whitish, base white, round apex with a black median line and barred with fuscous. Hindwings-bronzy-fuscous; cilia whitish-grey.

Christchurch; one specimen amongst bush, in January.

Endrosis, Hb.

Head smooth; ocelli present; tongue developed. Antennæ ⅘, in male strongly ciliated (2½), basal joint moderate, with pecten. Labial palpi long, curved, ascending, with appressed scales, terminal joint somewhat shorter than second, acute. Maxillary palpi very short, appressed to tongue.

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Posterior tibiæ clothed with long hairs above. Forewings with vein 1 furcate, 2 from ¾ of cell, 4 and 5 approximated at base, 7 and 8 stalked, 7 to costa, 11 from before middle. Hindwings somewhat narrower than forewings, elongate, long-pointed, tolerably acute, cilia 29; with an ill-defined hyaline patch towards base; veins 3 and 4 stalked, 5 absent, 6 and 7 parallel.

Only the one species is known. Stainton and Wocke both state the ocelli to be absent; they are, however, distinct, but placed close beneath the root of the antennæ, and therefore easy to be overlooked. A more singular and unaccountable error is that both these writers describe the antennæ as not ciliated, whereas the ciliations are unusually long for this group.

9. Endr. lacteella, Schiff.

(Gelechia subditella, Walk., 657; (?) G. adapertella, ib., 653.)

♂ ♀. 13–18mm. Head and thorax white. Palpi white, terminal joint with base and a subapical band black. Forewings elongate, narrow, pointed; pale greyish-ochreous, sprinkled with dark fuscous and a few white scales; a white basal dot; a basal patch enclosing this, a patch along costa towards middle, a small cloud on middle of inner margin, one at anal angle, and another at apex fuscous; a black dot beneath costa at ¼, a second, longitudinally elongate, rather obliquely beyond it on fold, a third beneath middle of costa, and a fourth in disc at ⅗: cilia pale whitish-ochreous, basal half sprinkled with dark fuscous. Hindwings whitish-grey; cilia pale whitish-ochreous.

Whangarei, Napier, Taranaki, Palmerston, Wellington, Christchurch, Bealey River, and Invercargill, probably therefore universally distributed; in houses, from October to March. Accidentally introduced from Europe, and common in Australia also; the larva feeds on seeds, dried foods, &c. Walker's type of Gelechia adapertella is much damaged, and its identification not quite certain.

Butalis, Tr.

Head smooth; ocelli present; tongue well-developed. Antennæ ⅘, in male filiform, shortly ciliated (½–1), basal joint moderate, without pecten. Labial palpi moderately long, curved, ascending, with appressed scales, terminal joint shorter than second, pointed. Maxillary palpi very short, slender, drooping. Posterior tibiæ clothed with long hairs above. Forewings with vein 1 simple or rarely shortly furcate, 2 from angle of cell, 3 absent, 7 and 8 stalked, 7 to hindmargin, 11 from about middle. Hindwings ½ to almost 1, lanceolate, cilia 1–4; veins all separate, and tolerably parallel.

A genus of considerable extent; it is cosmopolitan, but

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apparently most developed in Europe. The single New Zealand species approaches most to some of the Australian.

10. But. epistrota, n. sp.

♂ ♀. 10–11mm. Head, palpi, antennæ, thorax, abdomen, and legs rather dark grey, slightly bronzy-tinged, generally somewhat sprinkled with whitish; antennal ciliations ½; abdomen in female whitish beneath. Forewings lanceolate; rather dark bronzy-grey, more or less densely strewn with whitish scales; in paler specimens there are indications of two very ill-defined inwardly oblique darker streaks on anterior half, more distinctly spotted with darker on fold, and two less perceptible outwardly oblique streaks on posterior half; an obscure round dark fuscous dot in disc at ¾: cilia pale bronzy-grey. Hindwings ⅔ grey; cilia 2, pale bronzy-grey.

Christchurch (on the Lyttelton volcanic hills) and Mount Arthur (4,500ft.), in January; locally common.

Tineidæ.

Habrophila, n. g.

Head shortly rough-haired; ocelli present; tongue short. Antennæ in male—(?), filiform, basal joint moderately long, with strong pecten. Labial palpi long, slightly curved, somewhat ascending, second joint beneath with short, dense, rough, projecting tuft of scales towards apex; terminal joint much shorter than second, somewhat loosely scaled, tolerably obtuse. Maxillary palpi moderate, loosely scaled, folded. Posterior tibiæ with a few hairs beneath. Forewings with vein 1 simple, 2 from ¾ of cell, 5 and 6 approximated at base, 7 and 8 approximated at base, 7 to costa, 11 from before middle. Hindwings ⅔, lanceolate, cilia 2½; veins 2, 3, 4, remote and parallel, 5 and 6 stalked, 6 to hindmargin, 7 remote.

Allied to Endophthora. The single specimen has the apex of both antennæ broken, and their length is uncertain.

11. Habr. compseuta, n. sp.

♀. 11mm. Head, palpi, antennæ, and thorax whitish-ochreous, with a few dark fuscous scales. Abdomen ochreous-whitish. Legs pale whitish-ochreous, anterior pair infuscated. Forewings very elongate, narrow, parallel-sided, short-pointed; whitish-ochreous, suffusedly irrorated with dark fuscous, less towards base; costa marked with blackish-fuscous; a blackish dot on inner margin almost at base; an irregular series of blackish scales along fold; a small whitish spot on costa at ⅕; a large oblique subquadrate white spot on costa slightly before middle, reaching nearly half across wing; a small round black spot in disc before ¾, preceded by some blue-metallic scales;

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posterior half of wing suffused with golden-fuscous, crossed posteriorly by two slender angulated leaden-blue-metallic fasciæ, margined by series of white dots; hindmargin dotted with blackish and white: cilia ochreous-grey-whitish. Hindwings whitish-grey; cilia grey-whitish.

Mount Arthur (4,000ft.), in January; one specimen.

Argyresthiadæ.

Head more or less rough on crown, face smooth. Antennæ in male simple. Maxillary palpi obsolete. Forewings usually with a rough space on costa between veins 11 and 12.

The family is fairly well represented in Australia. I have only five New Zealand species, of which perhaps three are scarcely indigenous, but of Australian or exotic origin.

1. Forewings with vein 5 absent 3.
" " present 2.
2. Forewings with veins 7 and 8 stalked Circostola.
" " " separate Hofmannia.
3. Forewings with vein 10 absent Cateristis.
" " present Bedellia.

Hofmannia, Wk.

Head rough on crown, face smooth; ocelli present; tongue developed. Antennæ ¾, in male simple, subserrate, basal joint moderate, with pecten. Labial palpi moderately long, slightly curved, drooping, filiform, somewhat loosely scaled beneath, terminal joint shorter than second, sometimes more loosely scaled, tolerably pointed. Maxillary palpi obsolete. Posterior tibiæ smooth-scaled. Forewings with vein 1 furcate, 2 from near angle of cell, 7 to hindmargin, 9 and 10 sometimes from a point, 11 from about middle. Hindwings 1, lanceolate, cilia 2; vein 4 absent, 5 and 6 rather approximated, 6 to hindmargin.

A small genus, occurring in Europe and Australia.

12. Hofm. sphenota, n. sp.

♂. 13mm. Head and antennæ light ochreous-grey. Palpi grey. Thorax light ochreous. Abdomen whitish-ochreous. Legs fuscous, posterior pair ochreous-whitish. Forewings very elongate, very narrow, parallel-sided, long-pointed, acute; pale ochreous, thinly and irregularly sprinkled with dark fuscous and whitish; basal half of costa dotted with black; a moderately-broad ill-defined cloudy-white streak along inner margin from base to anal angle, pointed at extremities, interrupted at ⅔ by a small spot of ground-colour; a cloudy inwardly-oblique dark fuscous mark at ⅓ from near costa to near inner margin: cilia ochreous-grey-whitish, round apex ochreous, with base white, a grey line, and three cloudy dark grey bars. Hindwings pale whitish-grey; cilia ochreous-grey-whitish.

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Christchurch; one specimen amongst bush, in August. This species closely approaches an Australian form, and, my material being scanty, I am not sure that they are not to be regarded as local races only; however, at present I am disposed to consider them as distinct.

Circostola, n. g.

Head loosely scaled, rather rough behind, face smooth; ocelli present; tongue developed. Antennæ ¾, in male simple, filiform, basal joint moderate, with pecten of two or three fugitive scales. Labial palpi moderately long, curved, somewhat ascending, second joint with loose rough scales beneath towards apex, terminal joint somewhat shorter than second, loosely rough-scaled anteriorly, pointed. Maxillary palpi obsolete. Posterior tibiæ smooth-scaled. Forewings with vein 1 simple, 2 from ⅘ of cell, 7 and 8 stalked, 7 to hind-margin, 11 from ⅓. Hindwings 1, lanceolate, hindmargin sinuate beneath apex, cilia 1⅔; vein 4 absent, 5 and 6 rather approximated, 6 to hindmargin.

Intermediate in some respects between Zelleria and Argyresthia. The head is less rough than in any other genus of the family. Only the one species is known to me.

13. Circ. copidota, n. sp.

♂ ♀. 15–16mm. Head white, face ochreous-tinged. Palpi reddish-fuscous, terminal joint suffused with whitish. Antennæ ochreous-whitish, ringed with dark fuscous. Thorax white, shoulders ochreous-tinged. Abdomen ochreous-whitish. Legs whitish, anterior and middle pair irrorated and suffusedly tinged with dark fuscous. Forewings very elongate, narrow, costa strongly arched, apex very acute, produced, hindmargin obsolete; pale brownish-ochreous, with a few dark fuscous and whitish scales; a broad whitish streak along inner margin from base to middle, posteriorly attenuated to a point, and sometimes suffused, margined above by an irregular slender streak of black scales from base not reaching its apex; from extremity of this a slender irregular darker ochreous-brown suffused streak to apex of wing, marked with indications of blackish dots at ⅔ and apex: cilia pale whitish-ochreous, nearly white on costa at ¾, above apex brownish-ochreous, with a suffused blackish apical bar. Hindwings and cilia ochreous-grey-whitish.

Nelson, Wellington, Otira River (1,500ft.), and Lake Wakatipu (1,200ft.), in December and January; rather common amongst forest.

Cateristis, n. g.

Head rough on crown, face smooth; ocelli present; tongue developed. Antennæ ⅘, in male simple, serrate, basal joint

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moderately elongate, with large, dense, strong pecten. Labial palpi very short, filiform, drooping. Maxillary palpi obsolete. Posterior tibiæ densely clothed with very long hairs above and beneath. Forewings with vein 1 simple, 2, 3, and 4 almost from a point, 5 and 6 absent, cell open between 4 and 7, 7 and 8 stalked, 7 to hindmargin, 10 absent, 11 from middle. Hindwings ⅔, lanceolate, cilia 3; veins 3, 4, 5 absent, cell open between 2 and 6, 6 and 7 stalked, 6 to hindmargin.

The natural group to which this and the following genus belong I formerly regarded as a distinct family (Bedelliadæ), separable from the Argyresthiadæ proper by the hairy posterior tibiæ and degraded neuration of hindwings; but from a study of more extensive material I think it better to unite them. The structure of the head is characteristic and identical, and the change of neuration is gradual.

14.Cat. eustyla, n. sp.

♂. 10–11mm. Head and thorax white, face grey. Palpi dark fuscous. Antennæ whitish-grey. Abdomen grey. Legs dark grey, tarsi ringed with white, middle and posterior tibiæ grey-whitish. Forewings lanceolate; snow-white; costa slenderly dark fuscous from about ¼ to ¾: cilia light grey, towards base whiter, round apex wholly white or ochreous-white, with a grey dot. Hindwings and cilia light grey.

Christchuruch; one specimen amongst bush, in December. Also from Tasmania; the specimens from these two localities are absolutely similar.

Bedellia, Stt.

Head densely rough-haired above, face smooth; ocelli present; tongue short. Antennæ 1, in male filiform, simple, basal joint rather stout, with large dense pecten. Labial palpi short, porrected, slender, pointed. Maxillary palpi obsolete. Posterior tibiæ clothed with hairs above. Forewings with vein 1 simple, 2 from angle of cell, 3 from point with 2 or absent, 4 and 5 absent, 6 out of 8 or absent, 7 out of 8, running to hindmargin, 9 from point with 8, 11 from middle of cell. Hindwings ½, linear-lanceolate, cilia 6; no cell, veins 2, 3, 4 on a common stalk, 4 to apex, 5, 6, 7 absent.

15. Bed. somnulentella, Z.

♂ ♀. 8–9mm. Head whitish-ochreous, somewhat mixed with fuscous. Thorax whitish ochreous, in front fuscous. Forewings lanceolate; vein 3 absent, 6 out of 8; pale greyish-ochreous, suffusedly irrorated with fuscous except on a streak along inner margin: cilia light ochreous-grey, on costa ochreous-whitish. Hindwings grey; cilia light ochreous-grey.

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Larva mining blotches in leaves of Convolvulus and Ipomœa; pupa naked, suspended.

Dunedin; bred freely from the larva by Mr. A. Purdie. Occurs usually from September to November. Probably an introduced species, found in Europe, North America, and throughout Australia.

16. Bed. psamminella, n. sp.

♂ ♀. 9–10mm. Head light ochreous, crown mixed with dark fuscous. Palpi fuscous. Antennæ fuscous-whitish. Thorax and abdomen pale ochreous. Legs whitish-ochreous, anterior and middle pair infuscated. Forewings lanceolate; vein 3 present, 6 absent; pale brownish-ochreous, with a few minute black irrorations towards costa posteriorly; a small black dot on inner margin at ⅓ of wing: cilia pale brownish-ochreous. Hindwings light grey; cilia pale ochreous-grey.

Taranaki, Christchurch, and Dunedin, in September, and from December to February; common.

Elachistidæ.

Head smooth. Labial palpi curved, ascending, pointed. Maxillary palpi rudimentary. Hindwings lanceolate or linear.

In this family, as in the preceding, there is a strong tendency to degradation in the neuration. Where this exists, the neuration must not in all instances be considered of equal importance; in some cases the disappearance of one or two veins must be regarded as insufficient to warrant generic separation, where no variations appear in the other structure. The New Zealand indigenous species seem to be entirely of an Australian or South Pacific character.

1. Basal joint of antennæ dilated into a large eyecap 2.
Basal joint of antennæ not dilated 3.
2. Antennæ in ♂ with very long ciliations Vanicela.
" " naked Calicotis.
3. Antennæ in ♂ with very long ciliations Stathmopoda.
" " shortly ciliated or naked 4.
4. Terminal joint of palpi longer than second 5.
" " " not longer than second 6.
5. Antennæ in ♂ ciliated Limnæcia.
" " not ciliated Proterocosma.
6. Forewings with all veins present 7.
" " one or more veins absent 8.
7. Forewings with veins 7 and 8 stalked Syntomactics.
" " " " separate Thylacosceles.
8. Forewings with vein 11 absent Zapyrastra.
" " " present, from middle of cell 9.
9. Terminal joint of palpi somewhat roughened anteriorly Batrachedra.
Terminal joint of palpi smooth, slender Elachista.
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Head smooth; ocelli present; tongue developed. Antennæ almost 1, in male serrate, with very long fine ciliations (4), basal joint very broadly dilated and excavated beneath to form a large eyecap, with small pecten. Labial palpi long, curved, ascending, second joint smooth-scaled, terminal joint somewhat roughened above, as long as second, acute. Maxillary palpi very short, drooping. Anterior tibiæ and tarsi rather dilated with scales; posterior tibiæ and basal joint of tarsi clothed with stiff rough spines above, inner middle-spur spinose above on basal half, two basal joints of tarsi with short apical spines. Forewings with vein 1 furcate, 2 from ⅔ of cell, 7 to costa, 7 and 8 approximated at base, 11 from ⅔ of cell. Hindwings ½, linear, cilia 6; veins 2, 3, 4 parallel, 5, 6, 7 approximated at base.

A curious genus, allied to Stathmopoda, but very distinct. In repose the dilated anterior legs are extended in front; the posterior legs are not erected, but appear to be usually appressed to the abdomen, without touching the surface on which the insect rests. Only the two species are known to me.

17. Van. disjunctella, Walk.
(Vanicela disjunctella, Walk., 1,039.)

♂ ♀. 13–15mm. Head, palpi, antennæ, and abdomen white. Thorax white, posterior half dark bronzy-fuscous. Legs white, base of tarsal joints spotted with dark fuscous. Forewings linear, long-pointed; shining white, slightly yellowish-tinged; a dark bronzy-fuscous streak occupying dorsal half of wing, its upper margin notched at ¼, with a short oblique indentation in middle, opposite which is a white dot on inner margin, and with a short projection at ¾; beyond ¾ are one or two very fine dark fuscous longitudinal lines; apex irrorated or spotted with dark fuscous: cilia grey, with a black apical hook. Hindwings and cilia grey.

Whangarei, Auckland, Taranaki, Palmerston, Nelson, Masterton, and Wellington; apparently, therefore, universal throughout the North Island, but not yet met with in the South: common from December to March, amongst forest. The following undoubtedly distinct Australian species is so extremely similar that I describe it here for purposes of comparison.

18. Van. xenadelpha, n. sp.

♂ ♀. 12–15mm. Head, palpi, antennæ, and abdomen white. Thorax white, posterior half dark bronzy-fuscous. Legs white, base of tarsal joints obliquely streaked with dark fuscous. Forewings linear, long - pointed; shining white, faintly yellowish-tinged; a dark bronzy-fuscous streak occupying

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dorsal half of wing, its upper margin not notched, cut in middle by a slender inwards-angulated white line reaching inner margin, and with a very minute projection at ¾; a white dot on inner margin at ¼; a fine black longitudinal line in disc towards apex: cilia grey, with a black apical hook. Hindwings and cilia grey.

Sydney, New South Wales; only on the fence of the Botanical Gardens, where it is common from September to December. Readily distinguished from the preceding by the white dot on inner margin of forewings at ¼, the absence of the notch on dorsal streak, the junction of the central indentation and dot into an angulated line, and the minuteness of the projection at ¾; these, differences are entirely constant.

Stathmopoda, Stt.

Head smooth; ocelli present; tongue developed. Antennæ ¾, in male with very long fine ciliations (4–5), basal joint elongate, without pecten. Labial palpi very long, recurved, slender, smooth-scaled, terminal joint as long as second, acute. Maxillary palpi very short, drooping. Posterior tibiæ clothed with rough hairs above, posterior tarsi with projecting bristles at apex of two basal joints. Forewings with vein 1 furcate, 2 from near angle of cell, 2 and 3 sometimes partially obsolete, 7 and 8 stalked, 7 to costa, 11 from beyond ¾. Hindwings ½, linear-lanceolate, cilia 6; veins 2, 3, 4, 5 tolerably parallel, cell open between 5 and 6, 6 and 7 from a point.

This genus (of which the neuration is incorrectly given both by Stainton and Wocke) is represented in Europe by only one species (for the so-called Stathmopoda guerinii is generically quite distinct); but from Australia and New Zealand I have over thirty species, though the genus does not seem to have been identified elsewhere. It forms the type of a group, generally recognisable by the recurved palpi being directed sideways instead of forwards, the apical bristles of the tarsal joints, and the exceptional posture of the hindlegs in repose. In Stathmopoda the hindlegs are erected more or less perpendicularly over the back, the tarsi usually bent more sideways; but in some Australian species the insect does not always assume this posture, and sometimes does it with one leg only. Probably this attitude may be designed to deceive enemies by its unnatural appearance; it does not seem to imitate anything in particular. The occasional obsolescence of veins 2 and 3 of the forewings is an interesting phenomenon; from the examination of a good many denuded specimens I find no stress is to be laid on it; the obsolescence begins at the base of the veins, and appears in various degrees, sometimes only the extreme tips of the veins remaining. The genus differs from all others of the family, except Vanicela, by the very long

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antennal ciliations of the male. I may add that the European and North American genus Schreckensteinia, Hb. (Chrysocorys, Curt.), belongs to this group.

1. Forewings without markings holochra.
" with markings 2.
2. Forewings deep ochreous-yellow phlegyra.
" whitish-ochreous or whitish 3.
3. Forewings with a dark fuscous V-shaped anterior mark campylocha.
" without a dark fuscous V-shaped anterior mark 4.
4. Posterior tibiæ with conspicuous black apical ring of scales epichlora.
" " without conspicuous black apical ring of scales skelloni.

19. Stath. holochra, n. sp.

♀. 14mm. Head, palpi, antennæ, and abdomen pale whitish-ochreous. Thorax whitish-ochreous, slightly reddish-tinged. Legs pale whitish-ochreous. Forewings elongate, very narrow, broadest near base, long-pointed; pale reddish-ochreous, unicolorous: cilia pale whitish-ochreous-grey. Hindwings pale whitish-grey, posteriorly ochreous-tinged; cilia pale whitish-ochreous-grey.

Wellington; one specimen in December.

20. Stath. phlegyra, n. sp.

♂ ♀. 12–16mm. Head, palpi, and antennæ whitish-ochreous. Thorax ochreous-yellowish, shoulders and a central spot sometimes greyish-tinged. Abdomen pale whitish-ochreous, greyish-tinged. Legs pale whitish-ochreous, anterior pair dark fuscous. Forewings elongate, very narrow, broadest near base, long-pointed; deep ochreous-yellow; a rather broad ashy-grey streak along costa from base to near apex; a short indistinct streak on fold at ⅓, an irregular spot in disc before middle, and a short irregular longitudinal streak in disc about ⅔, fuscous or grey, tending to be variously suffused together or with costal streak, or frequently more or less wholly obsolete: cilia light grey. Hindwings and cilia light grey.

Auckland, Taranaki, Palmerston, and Wellington; common amongst forest, from January to March. It is a variable species, but always recognisable by the deep ochreous-yellow ground-colour.

21. Stath. campylocha, n. sp.

♂ ♀. 12–14mm. Head and thorax whitish-ochreous, somewhat metallic-shining. Palpi and antennæ pale whitish-ochreous. Abdomen grey. Legs whitish-ochreous, greyish-tinged, anterior pair dark grey, posterior tibiæ with dark-grey scales at origin of spurs. Forewings elongate, very narrow,

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broadest near base, long-pointed; whitish-ochreous; an ochreous-fuscous or dark fuscous streak along costa from base to ¾, sometimes almost obsolete; an ochreous-fuscous or dark fuscous broadly V-shaped mark before middle, more or less suffused, variable in thickness, its angle resting on inner margin, extremities nearly reaching costa; a longitudinal line in posterior half of disc, a spot at apex, and an elongate spot at anal angle ochreous-fuscous or ochreous, sometimes partially connected: cilia grey. Hindwings rather dark grey; cilia grey.

Wellington and Dunedin; five specimens in January and February, amongst forest. Also variable; in addition to the conspicuous dark V-shaped mark of the forewings, the darker grey hindwings and grey abdomen are good distinguishing characters.

22. Stath. skelloni, Butl.
(Boocara skelloni, Butl., “Cist. Ent.,” ii., 562.)

♂ ♀. 12–15mm. Head, palpi, and antennæ pale whitish-ochreous. Thorax whitish-ochreous. Abdomen pale whitish-ochreous, greyish-tinged. Legs pale whitish-ochreous, anterior pair infuscated, apex of posterior tibiæ grey. Forewings elongate, very narrow, broadest near base, long-pointed; whitish-ochreous, sometimes yellowish-tinged; markings grey, very variable, sometimes partially margined by an ochreous suffusion; normally an elongate spot on inner margin at ⅓, a second beneath costa in middle, a third in disc at ⅔, a fourth before apex, and a slender subcostal line from second spot to costa near apex, but these tend to be variously connected and confused; sometimes a streak along fold, or along anterior part of costa; rarely a dark ochreous-fuscous suffusion towards base of inner margin: cilia light grey, sometimes ochreous-tinged. Hindwings and cilia light grey.

Taranaki, Wellington, Blenheim, Nelson, Christchurch, Dunedin, Lake Wakatipu, and Invercargill; common amongst bush, from December to March, but seeming to disappear towards the north. Butler failed to recognise the genus; but it is fortunately unnecessary to consider how to treat his grotesquely solecistic generic name.

23. Stath. epichlora, n. sp.

♀. 9–11mm. Head, palpi, antennæ, thorax, abdomen, and legs whitish; anterior legs blackish in front, posterior tibiæ with a sharp black apical ring of scales, preceded above by some grey hairs. Forewings elongate, very narrow, broadest near base, long-pointed; whitish, more or less mixed with ochreous or grey in disc; markings rather dark fuscous, but cloudy and ill-defined; a small spot oil inner margin at ⅓, a second more conspicuous on inner margin beyond middle, and

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an angulated fascia-like spot towards apex: cilia whitish-grey. Eindwings and cilia whitish-grey.

Auckland, Wellington, and the Otira River (1,500ft.); six specimens amongst forest, in December and January. A distinct but inconspicuous species.

Calicotis, n. g.

Head smooth; ocelli present; tongue rudimentary. Antennæ ¾, in male rather stout, filiform, basal joint broadly dilated, excavated beneath to form an eyecap, rough-scaled on posterior edge, without pecten. Labial palpi long, curved, ascending, smooth-scaled, terminal joint shorter than second, acute. Maxillary palpi obsolete. Middle tarsi with long projecting spines at apex of two basal joints; posterior tibiæ clothed with dense long rough hairs above and beneath, posterior tarsi with whorls of long projecting spines at apex of all joints. Forewings with vein 1 simple, 2 and 3 absent, 4 from angle of cell, 7 and 8 stalked, 7 to costa, 11 from ⅚ of cell. Hindwings ½, linear, cilia 7; vein 4 absent, cell open between 3 and 6, 5 free rising from base, 6 and 7 from a point.

Allied to Stathmopoda, but differing especially by the greatly dilated and excavated basal joint of antennæ, and by the entire absence of the long antennal ciliations. In repose the imago bends the posterior legs to form an angular arch, and extends them horizontally at right angles to the body. The habits of the larva are known, and interesting.

24. Cal. crucifera, n. sp.

♂ ♀. 9–12mm. Head, palpi, antennæ, thorax, abdomen, and legs very pale whitish-ochreous; terminal joint of palpi with a dark fuscous line on outer edge; anterior legs suffused with blackish in front, posterior legs spotted with black on apex of joints. Forewings elongate, very narrow, broadest near base, long-pointed; ochreous-whitish, more or less irregularly suffused or blotched with ochreous; a small cloudy dark fuscous spot on inner margin near base, and another on costa slightly before middle, both in female sometimes almost obsolete; an apical black dot: cilia grey-whitish. Hindwings whitish-grey; cilia grey-whitish.

Larva 16-legged, moderately stout, cylindrical, active; whitish flesh-colour, or whitish; head pale whitish-brown. Feeds on Platycerium grande (a large parasitic fern, growing on tree-trunks), burrowing amongst the ripe fructification beneath the fronds, forming galleries of loose refuse; found in March,

Taranaki and Palmerston, in February and March; common amongst its food. The species occurs also plentifully in the Botanical Gardens at Sydney, but I have not yet met

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with it in native forest in Australia, and it is therefore at least possible that it was introduced into Sydney with ferns from New Zealand. The food-plant is, however, considered native in both countries.

Thylacosceles, n. g.

Head smooth; ocelli present; tongue developed. Antennæ ⅚, in male stout, very shortly ciliated (½), basal joint moderate, without pecten. Labial palpi very long, slender, recurved, smooth-scaled, terminal joint as long as second, acute. Maxillary palpi obsolete. Posterior tibiæ with long hairs above, with a large dense triangular tuft of long scales covering terminal half above, tarsi with long projecting spines at apex of two basal joints. Forewings with vein 1 furcate, 2 from ⅔ of cell, 3 from angle, 7 to costa, 11 from ¾ of cell. Hindwings ½, linear-lanceolate, cilia 6; veins 2, 3, 4, 5 tolerrably parallel, 6 and 7 approximated at base.

Allied to Stathmpoda; sufficiently distinguished by the very short antennal ciliations, and peculiar tuft of tibiæ, apart from the neuration; the latter, I believe, I have made out correctly, but cannot be sure on my single specimen, which proved difficult of examination. In repose the imago holds the posterior legs so as to project behind and rest on the surface, but with the tibiæ and tarsi bent so as to form an erect triangle with the surface on which it rests; hence with much the superficial appearance of the hindlegs of a grasshopper.

25. Thyl. acridomima, n. sp.

♂. 11mm. Head and palpi light yellowish-ochreous. Antennæ whitish-fuscous, base yellowish. Thorax fuscous. Abdomen grey. Anterior legs dark fuscous; middle legs ochreous-yellowish; posterior legs ochreous-whitish, tibiæ with a black apical ring, and tuft of posterior half dark grey. Forewings elongate, very narrow, broadest near base, long-pointed; fuscous, somewhat unevenly shaded, but without markings: cilia light fuscous. Hindwings fuscous-grey; cilia light fuscous.

Wellington; one specimen in January.

Zapyrastra, n. g.

Head smooth; ocelli present; tongue developed. Antennæ ⅘, in male subserrate, slightly thickened towards apex, basal joint elongate, obconical, without pecten. Labial palpi moderate, curved, ascending, slender, smooth, terminal joint shorter than second, acute. Maxillary palpi rudimentary. Posterior tibiæ thinly haired above on basal half and at apex. Forewings with vein 1 furcate, 2 from rather near angle of

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cell, 7 and 8 stalked, 7 to costa, 10 from near angle, 11 absent. Hindwings ½, linear-lanceolate, cilia 5; veins 2, 3, 4 parallel, cell open between 4 and 5, 5 and 6 stalked, 6 to close below apex, 7 approximated to 6 at base.

Allied to the European genus Chrysoclista, from which it differs principally in the neuration of forewings. The group of Laverna, to which it belongs, although extensively represented in Australia, has probably no truly indigenous representatives in New Zealand; the present species, common to both countries, is in all probability really Australian, and has found its way over within comparatively recent times.

26. Zap. calliphana, n. sp.

♂ ♀. 5–8mm. Head, palpi, antennæ, thorax, abdomen, and legs dark shining bronze, face whitish-bronze, legs spotted with white. Forewings lanceolate; bright dark golden-bronze; markings pale violet-golden-metallic; a fascia near base, often ill-defined; a nearly perpendicular fascia before middle; a dot in disc beyond middle, beneath which is a black dot or small spot on fold; an inwardly-oblique fascia at ¾; a small spot on anal angle; a streak along hindmargin from apex; a triangular snow-white spot on costa near apex: cilia fuscous-grey, round apex with two blackish lines, and a minute white dot above apex. Hindwings dark fuscous; cilia fuscous-grey.

Christchurch and the Bealey River; rather common from December to February, frequenting Leptospermum, on which the larva must certainly feed. The species is common also in New South Wales and Tasmania, frequenting the same plant, from September to April.

Limnœcia, Stt.

Head smooth; ocelli absent; tongue developed. Antennæ ¾, in male serrate, moderately ciliated (1), basal joint very elongate, dilated towards apex, with one or two hair-scales at base. Labial palpi very long, recurved, second joint thickened with appressed scales, terminal joint longer than second, acute. Maxillary palpi rudimentary. Thorax in male with a long fine curved pencil of hairs from each side beneath, directed backwards. Posterior tibiæ clothed with long hairs above. Forewings with vein 1 furcate, 2 from ⅔ of cell, 7 and 8 stalked, 7 to costa, 11 from before middle of cell. Hindwings ⅔, elongate-lanceolate, cilia 2; veins all separate and tolerably parallel.

Stainton was undoubtedly mistaken in reuniting this genus to Laverna, to which it is by no means closely allied, differing in several essential points.

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27. Limn. phragmitella, Stt.

♂ ♀. 15–21mm. Head and thorax pale ochreous. Palpi whitish-ochreous, terminal joint with a longitudinal dark fuscous line. Forewings elongate, very narrow, long-pointed; whitish-ochreous, brownish-tinged; a round dark fuscous dot in disc before middle, and a second at ⅔, tending to be ringed with ochreous-whitish, and connected by an obscure streak of ochreous-whitish scales somewhat mixed with fuscous; beyond the second dot is generally a small fuscous spot: cilia whitish-ochreous. Hindwings pale grey, ochreous - tinged; cilia whitish-ochreous.

Larva yellow-whitish, with five brownish longitudinal lines; feeding in seedheads of Typha angustifolia, burrowing amongst the seeds, and causing the down to hang out in loose masses, exactly in the manner of Scieropepla typhicola.

Hamilton; one specimen in January, amongst the swamps of the Waikato. I have also taken it in New South Wales. The species occurs in Central Europe, but is not very widely known, probably owing to the retired habits of the imago. My specimens are the only ones taken outside Europe; yet, as it is hardly conceivable that the species should have been artificially introduced, and as the Typha is thought to be indigenous in suitable localities all round the world, I conjecture that the insect may be truly cosmopolitan. The light down of the seedheads, carrying the seeds of the plant and the ova of the insect, must be exceedingly susceptible of dissemination by the wind.

Syntomactis, n. g.

Head smooth; ocelli absent; tongue developed. Antennæ ¾, in male serrate, pubescent, basal joint very elongate, with pecten. Labial palpi moderately long, curved, ascending, second joint with loose rough scales beneath towards apex, terminal joint as long as second, slightly roughened anteriorly, acute. Maxillary palpi very short, appressed to tongue. Thorax in male with some very long fine hairs beneath from posterior extremity. Posterior tibiæ clothed with long hairs above. Forewings with vein 1 furcate, 2 from angle of cell, 5 and 6 out of 7, 7 to costa, 8 out of 7 before 6, 11 from middle. Hindwings ½, linear-lanceolate, cilia 6; veins 2, 3, 4 parallel, 5 from a point with 6, 6 and 7 stalked.

Allied to the group of Laverna, but not very closely approaching any particular genus.

28. Synt. deamatella, Walk.

(Gelechia deamatella, Walk., 654.)

♂ ♀. 11–12mm. Head ochreous-white. Palpi white, second joint with basal half black, and apical and subapical ochreous rings, terminal joint with basal half black. Antennæ whitish,

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obscurely ringed with blackish. Thorax white, or whitish-ochreous. Abdomen pale yellowish - ochreous, posteriorly greyer. Legs blackish, ringed with ochreous-white. Forewings very elongate, narrow, long-pointed; greyish-ochreous, coarsely and irregularly irrorated with dark fuscous; markings white, tending to be margined by a black suffusion; a triangular spot on costa before ¼, its apex sometimes almost reaching inner margin; an irregular somewhat oblique blotch beyond middle, touching costa anteriorly, and almost reaching inner margin; a small ill-defined, irregular, transverse spot near apex, most distinct on costa: cilia pale ochreous-greyish, round apex somewhat mixed with fuscous. Hindwings grey; cilia pale ochreous-grey.

Christchurch and Invercargill in December, February, and March; six specimens, amongst bush.

Proterocosma, Meyr.

Head smooth; ocelli present or absent; tongue developed. Antennæ ⅘ to 1, in male serrate, pubescent or simple; basal joint elongate, with pecten. Labial palpi very long, recurved, smooth, slender, terminal joint longer than second, acute. Maxillary palpi rudimentary. Posterior tibiæ clothed with hairs above. Forewings with vein 1 furcate, 2 from ⅘ of cell, 5 sometimes out of 7, 6 out of 7 or absent, 7 to costa, 8 out of 7, 11 from before middle. Hindwings about ½, linear-lanceolate, cilia 3 to 6; veins 2, 3, 4 parallel, 5 approximated to 4, 6 and 7 from a point, or stalked, or rarely coincident.

This interesting genus, which is rather an old type of the family, and indicates the origin of some more widely-distributed forms, is rather extensively distributed in Australia, and I have also described several species from the South Pacific islands. Of the three New Zealand species, the first two are endemic, but markedly allied to Australian forms, the third is widely distributed in Australia.

1. Forewings with clear white lines apparitella.
" without clear white lines 2.
2. Forewings with irregular white markings, irrorated with black aëllotricha.
Forewings with defined round black dots anarithma.

29. Prot. apparitella, Walk.

(Gelechia apparitella, Walk., 1,027.)

♂ ♀. 9–13mm. Head and thorax golden-ochreous, face white, eyes crimson. Palpi ochreous, more or less suffused with white, terminal joint white with anterior edge and often apex black. Antennæ white, ringed with black. Abdomen whitish-ochreous. Legs whitish, banded with dark fuscous, posterior pair pale whitish-ochreous. Forewings elongate, very narrow, long-pointed; vein 5 separate, 6 present; golden-

– 175 –

ochreous, paler towards costa posteriorly; markings snow-white, finely black-margined; a very slender median line from base to ¼; a slender oblique line from costa at ⅕, terminating in a moderate triangular spot on inner margin before, middle, which is either wholly white, or white with an ochreous centre; or wholly ochreous and scarcely paler than ground-colour; a line from ⅖ of costa almost perpendicularly half across wing, thence abruptly rectangularly bent outwards to middle of disc, and again rectangularly bent to inner margin; a fine, extremely oblique line from middle of costa to disc at ¾, thence acutely angulated to anal angle, sinuate inwards beneath costa, connected with preceding line on costa by a fine white line, and on inner margin by a streak which is either white, or ochreous hardly paler than ground-colour; a whitish-ochreous or white, posteriorly black-margined, mark on costa at ⅘, whence proceeds a black sometimes ill-defined line to apex; sometimes an irregular short white streak along hindmargin to apex: cilia light greyish-ochreous, round apex more golden-ochreous, with a black dot at base on apex. Hindwings with veins 6 and 7 stalked; costa in male with long loose hairs at base; grey; cilia light ochreous-greyish.

Auckland and Wellington; common amongst forest, in December and January.

30. Prot. aëllotricha, n. sp.

♂ ♀. 10–12mm. Head and thorax reddish - ochreous; face ochreous-whitish. Palpi white, second joint with three ochreous rings, terminal joint with three black rings. Antennæ white, ringed with black. Abdomen grey, towards base pale-ochreous. Legs whitish, banded with blackish. Forewings elongate, very narrow, long-pointed; vein 5 separate, 6 present; reddish-ochreous, tending to become whitish-ochreous round markings and towards base of inner margin; markings ochreous-white, closely irrorated with black; an irregular oblique fascia from ¼ of costa, not reaching inner margin, emitting a short streak from posterior edge above middle; an irregular somewhat 8-shaped spot in middle of disc, from upper part of which proceeds an irregular streak to costa before apex; an irregular ochreous-whitish streak along hindmargin from apex to anal angle; a black apical dot: cilia light ochreous-greyish, round apex reddish-ochreous, with a blackish basal line and two blackish apical hooks. Hindwings with veins 6 and 7 stalked; grey; cilia pale-grey, ochreous-tinged.

Hamilton; two specimens in January.

31. Prot. anarithma, n. sp.

♂ ♀, 7–10mm. Head and thorax brownish-ochreous, face ochreous-whitish. Palpi ochreous-whitish, second joint with

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basal half and a subapical ring suffusedly irrorated with black, terminal joint irrorated with dark fuscous. Antennæ whitish-ochreous, ringed with dark fuscous. Abdomen grey-whitish, or grey. Legs dark grey, suffusedly ringed with whitish. Forewings lanceolate; vein 5 separate, 6 present; brownish-ochreous, sometimes more or less sprinkled with dark fuscous; a black dot on base of costa, sometimes obsolete, a second on costa near base, a third in disc beneath second, a fourth on base of inner margin, often obsolete, a fifth in disc before middle, a sixth on fold rather obliquely beyond fifth, and a seventh in disc at ⅔; generally two small indistinct whitish-ochreous spots on costa and inner margin opposite seventh dot: cilia light grey, darker round apex. Hindwings with veins 6 and 7 from a point; grey; cilia light-grey.

Taranaki, Palmerston, Napier, and Masterton; from January to March, in some places exceedingly plentiful, but apparently not found everywhere. Around Taranaki I found it swarming in grassy places; it has quite the habits of an Elachista, and is probably a grass-feeder. It is very widely-distributed through Australia from east to west, but there also is local, and abundant in some places only.

Elachista, Stt.

Head smooth; ocelli present; tongue developed. Antennæ ¾, in male simple, filiform or serrulate, basal joint moderate, with or without pecten. Labial palpi long, recurved, slender, smooth-scaled, terminal joint shorter than second, acute. Maxillary palpi obsolete. Posterior tibiæ clothed with long hairs above and beneath. Forewings with vein 1 simple, 2 from angle of cell, 4 sometimes absent, 5 absent, 6 out of 7, 7 to costa, 8 out of 7 or absent, 9 approximated to or from point with or out of 7, 11 from middle. Hindwings about ½, narrow lanceolate, cilia 3 to 5; vein 4 sometimes absent, 5 absent, cell sometimes open below 6, 6 and 7 stalked.

A genus of considerable extent, and probably cosmopolitan, but from the obscurity of the species hitherto not much noticed outside Europe. Besides the seven New Zealand species, I have about fifteen Australian. All known larvæ of the genus mine in leaves of grasses or sedges. Wocke separates the species in which vein 4 of both wings is absent (it appears to change in both wings simultaneously) as a distinct genus, under the name Pæciloptilia; but, after careful consideration, this appears to me unnecessary: there is no other difference whatever, and, as I have remarked above, in this family the disappearance of a vein is not of great importance, and the neuration of many of its genera is liable to vary to that extent. I have therefore retained all in one genus, but used the character to separate it into sections.

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1. Palpi wholly white or whitish 2.
" partly grey 4.
2. Forewings irrorated with grey exaula.
" not irrorated with grey 3.
3. Head and thorax striped with brown and white thallophora.
" not striped with brown and white helonoma.
4. Terminal joint of palpi wholly white or whitish 5.
" " not wholly white or whitish 6.
5. Forewings with obscure dark fuscous streaks in disc ombrodoca.
Forewings without obscure dark fuscous streaks in disc gerasmia.
6. Forewings dark grey archæonoma.
" whitish-grey melanura.

§ A. Vein 4 of both wings present.

32. Elach. melanura, n. sp.

♂. 13mm. Head, palpi, antennæ, and thorax whitish-grey. Abdomen ochreous-whitish, with a dense black apical exsertible tuft. Legs dark fuscous, posterior pair ochreous-whitish. Forewings lanceolate; whitish-grey, somewhat irrorated with darker; an elongate black dot on fold before middle, a second in disc above middle, and a third in disc at ⅔: cilia grey-whitish, with a spot of black scales at base round apex, and tips sprinkled with black. Hindwings and cilia pale whitish-grey.

Hamilton; one specimen in January. I have two specimens from Australia which closely resemble this, and which agree in possessing the characteristic and highly peculiar black anal tuft; but, as they differ considerably from the New Zealand specimen, and also from one another, in the position of the black dots on the forewings, I have not felt justified at present in uniting them, although I think it very probable that a longer series of specimens may prove this character to be variable.

33. Elach. gerasmia, n. sp.

♂ ♀. 9–14mm. Head whitish. Palpi grey, terminal joint and apex of second white. Antennæ grey. Thorax whitish-grey. Abdomen grey-whitish, anal tuft in male more or less ochreous-tinged. Legs dark grey, posterior pair grey-whitish. Forewings lanceolate; light grey or rarely grey-whitish; a black dot on fold in middle, and an elongate black dot in disc at ⅔: cilia grey, with indications of two black lines for a short distance below apex. Hindwings and cilia grey.

Hamilton, Makatoku, and Invercargill; common in swampy places, in December, January, and March.

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34. Elach. thallophora, n. sp.

♂ ♀. 8–15mm. Head ochreous-whitish, with a central longitudinal ochreous-brown stripe. Palpi white. Antennæ whitish-fuscous. Thorax brown, with an ochreous-white stripe on each side of back. Abdomen grey, anal tuft ochreous-whitish. Legs dark fuscous, posterior pair whitish. Forewings lanceolate; pearly white; an ochreous-brown longitudinal streak from base of costa, and another from base in middle, converging to a point in disc at ⅘, where they terminate; an ochreous-brown streak along inner margin from base to anal angle; in male these markings are thicker, darker, and more suffused, and posterior half of costa is also suffused with brown: cilia in male whitish-fuscous, in female ochreous-whitish, beneath anal angle fuscous-tinged. Hindwings grey; cilialight grey.

Christchurch (on sandhills) and Mount Arthur (4,000ft.), in January and March; locally abundant. The variation in size is noteworthy, some of the largest females being twice as large as the males. The species is a remarkably distinct one, but recalls E. rufocinerea, to which it has probably some real relationship.

§ B. Vein 4 of both wings absent.

35. Elach. helonoma, n. sp.

♂ ♀. 8–10mm. Head and thorax ochreous-whitish, sprinkled with ochreous. Palpi white. Antennæ fuscous. Abdomen grey-whitish, anal tuft ochreous-whitish. Legs dark fuscous, posterior pair ochreous-whitish. Forewings lanceolate; whitish, more or less irrorated with ochreous, especially on dorsal half; a slender ochreous-fuscous median longitudinal streak from near base to middle, and a second from above extremity of first to near apex; a fuscous dot beneath apex of first streak, sometimes obsolete; inner margin more or less obscurely brownish towards base: cilia grey-whitish. Hindwings pale grey; cilia grey-whitish.

Christchurch, on the Port Hills; in January and March, abundant amongst the tussock-grass, to which it appears attached.

36. Elach. exaula, n. sp.

♂. 9–10mm. Head and palpi ochreous-whitish. Antennæ fuscous. Thorax whitish-ochreous irrorated with grey. Abdomen grey, anal tuft whitish-ochreous. Legs dark grey, ringed with whitish, posterior tibiæ whitish. Forewings lanceolate; pale whitish-ochreous, irrorated with grey, more closely and suffusedly on costa, more yellowish-tinged in disc; a slender black median streak from near base to before middle; a black elongate dot in disc above middle, and a second, larger

– 179 –

and more distinctly elongate, below it; a slender black median streak from ⅔ to near apex: cilia light grey, round apex ochreous-whitish with a fine black line. Hindwings grey; cilia light grey.

Mount Arthur (4,000ft.); three specimens in January.

37. Elach. ombrodoca, n. sp.

♂ ♀. 6–9mm. Head grey-whitish, in male irrorated with dark grey. Palpi dark grey, terminal joint and apex of second whitish. Antennæ grey. Thorax grey-whitish, irrorated with dark grey. Abdomen grey, anal tuft ochreous-whitish. Legs dark grey, apex of joints whitish, posterior tibiæ ochreous-whitish. Forewings lanceolate; ochreous-whitish, in male densely irrorated throughout with dark grey, in female more sparsely; an indistinct slender dark fuscous streak along fold from near base to ⅓; a cloudy dark-grey spot beneath costa slightly before middle, and another larger and more blackish obliquely beyond it near inner margin; preceding these are faint indications of an oblique paler fascia, more distinct in female; an indistinct short longitudinal dark fuscous streak in disc about ⅔; slightly beyond this are very faint indications of two paler marginal spots, appearing to form an angulated fascia: cilia whitish-grey, ochreous-tinged, round apex more ochreous-whitish with a fine black line. Hindwings grey; cilia light grey.

Christchurch, Dunedin, and Invercargill; in August and September, and from February to April, very common in waste grassy places, as by roadsides.

38. Elach. archæonoma, n. sp.

♂ ♀. 6–8mm. Head, palpi, and thorax whitish irrorated with dark grey. Antennæ grey. Abdomen grey, anal tuft in male grey, in female ochreous-whitish. Legs dark grey, ringed with whitish. Forewings lanceolate; dark grey, irrorated with whitish; basal area in female distinctly paler; an oblique pale fascia before the middle, in male very obscure and indistinct, in female white and conspicuous; beyond this is a more or less defined blackish suffusion, tending to form two separate spots, lower more marked; indications of a short longitudinal dark fuscous streak in disc about ⅔; in female two conspicuous white opposite almost connected spots beyond ⅔, in male not traceable: cilia grey, with a fine black line round apex, in female with a distinct white apical spot. Hindwings and cilia grey.

Auckland, Nelson, Wellington, and Dunedin; common in grassy places by roadsides, in December and January. The very considerable dissimilarity between the sexes is the same as occurs in some European species, as E. obscurella.

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Batrachedra, Stt.

Head smooth; ocelli present; tongue developed. Antennæ ⅚, in male filiform, simple, basal joint short, without pecten. Labial palpi moderately long, recurved, second joint with scales more or less slightly projecting angularly in front at apex, sometimes produced into a short dense tuft, terminal joint shorter than second, somewhat roughened with scales anteriorly, acute. Maxillary palpi very short, drooping. Posterior tibiæ with short tolerably-appressed hairs above. Forewings with vein 1 obsoletely furcate, 2 from near angle of cell, 3 absent, 6 and 7 sometimes stalked, 7 to costa, 8 absent, 11 from near middle. Hindwings ½, linear-lanceolate or linear, cilia 5–8; 2 and 3 sometimes absent, cell open between 4 and 5, 5 approximated to or out of 6 or absent, 6 and 7 approximated.

A genus containing at present two European species, probably two or three North American, about twenty Australian, and three from New Zealand. There is considerable variation in the scaling of the second joint of palpi, which sometimes forms a well-marked projecting tuft in front, whilst more commonly it appears only as a very slight projection, but these are essentially modifications of the same type, and are connected by such intermediate gradations that no separation is possible; and also in the neuration of the hindwings, where some of the veins are liable to disappear, but here also every gradation is found. The species are very similar in appearance and habit; probably most of the larvæ feed on the seeds of rush (Juncus).

1. Forewings white psithyra.
" pale ochreous 2.
2. Palpi with second joint tufted in front eucola.
" " not tufted in front arenosella.

39. Batr. eucola, n. sp.

♂. 19mm. Head and antennæ whitish-ochreous. Palpi whitish-ochreous, terminal joint and apex of second more brownish, second joint with scales projecting in front into an angular tuft. Thorax pale brownish-ochreous. Abdomen whitish-ochreous. Legs dark fuscous, apex of joints whitish-ochreous. Forewings elongate, very narrow, parallel-sided, long-pointed; veins 6 and 7 stalked; whitish-ochreous, somewhat sprinkled with brownish-ochreous, towards costa broadly suffused with brownish-ochreous, costal edge fuscous towards base; a dark fuscous dot in disc before middle, a second on fold obliquely before first, and a third, larger and somewhat transverse, in disc before ¾: cilia whitish-ochreous, beneath anal angle greyish-tinged, on costa marked with three dark fuscous dots, with indications of two dark fuscous lines at

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apex only. Hindwings with all veins present; grey, slightly ochreous-tinged; cilia light grey, slightly ochreous-tinged, on costa whitish-ochreous.

Bealey River; one specimen in January. This is the largest species of the whole genus known, with the most pronounced tuft of palpi, and the full neuration of hindwings.

40. Batr. arenosella, Walk.
(Gracilaria arenosella, Walk., 857.)

♂ ♀. 11–14mm. Head and thorax whitish-ochreous. Palpi whitish-ochreous, apex of second joint blackish, scales slightly projecting, terminal joint more whitish, with sub-median and apical black rings. Antennæ whitish-ochreous, indistinctly ringed with fuscous, towards apex with three or four broader fuscous bands. Abdomen ochreous-grey-whitish. Legs dark fuscous, ringed with, whitish, posterior tibiæ ochreous-whitish irrorated with dark fuscous. Forewings elongate, very narrow, long-pointed; veins 6 and 7 separate; pale yellow-ochreous, finely sprinkled with dark fuscous; a dark fuscous dot in disc before ⅖, and another at ⅘, occasionally obsolete: cilia pale grey, on costa whitish-ochreous, sharply divided at apex. Hindwings with veins 2, 3, and 5 absent; pale grey; cilia pale grey.

Larva feeds amongst seeds of Juncus, joining them together with a slight web, in August: pupa very slender, in a cocoon amongst the seeds.

Palmerston, Wellington, and Christchurch; common from January to March. Also, generally distributed in east and south Australia, which is doubtless its place of origin. The species is closely allied in every way to the European B. pinicolella.

41. Batr. psithyra, n. sp.

♂. 7–10mm. Head, thorax, and abdomen pearly white. Palpi white, second joint with a blackish sub-apical ring, scales slightly projecting, terminal joint with a blackish basal ring. Antennæ white, indistinctly ringed with pale fuscous. Legs white, indistinctly banded with fuscous. Forewings elongate, very narrow, long-pointed; veins 6 and 7 stalked; white, more or less sprinkled with fuscous; a dark fuscous elongate dot in disc before middle, a second very obliquely before it on fold, and a third in disc beyond ⅔; a sharply-marked black apical dot: cilia whitish, with a black line opposite apex only. Hindwings with veins 2, 3, and 5 absent; whitish; cilia whitish.

Auckland, Hamilton, Wellington, Nelson, and Invercargill; ten specimens, in December and January.

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Gracilaridæ.

Head smooth, or rough on crown (not in New Zealand genera). Antennæ nearly as long as forewings or longer, simple. Maxillary palpi developed. Labial palpi slender, ascending. Forewings with vein 1 simple, 11 from before middle of cell. Hindwings lanceolate or linear, cell open. Larva 14-legged.

The New Zealand species of this family have apparently no near specific relationship to the Australian; possibly they have more affinity with the South American, which are insufficiently known.

1. Palpi with second joint tufted beneath Coriscium.
" " not tufted beneath 2.
2. Posterior tibiæ rough-haired above Conopomorpha.
" " smooth above Gracilaria.

Gracilaria, Z.

Head smooth; ocelli absent or rarely present; tongue developed. Antennæ 1 or over 1, in male filiform, slender, basal joint moderate, without pecten. Labial palpi long, curved, ascending, smooth-scaled, second joint sometimes loosely scaled beneath towards apex, terminal joint almost as long as second, acute. Maxillary palpi moderately long, filiform, porrected. Middle tibiæ sometimes dilated with scales, posterior tibiæ smooth-scaled. Forewings with vein 1 simple, 2 from ⅚, 3 sometimes absent, 4 and 5 often approximated, 7 to costa, 11 from before middle or near base, secondary cell sometimes well defined. Hindwings about ½, lanceolate or linear-lanceolate, cilia 4–5; 3 sometimes absent, cell open between 4 and 5, 5 and 6 stalked, their stalk sometimes continued to base of wing, 7 from angle of cell, or rarely out of 6.

The larvæ are usually leaf-miners, or less commonly roll leaves into a peculiar conical chamber; but the only known New Zealand larva is exceptional in the genus, living in spun-up shoots like an ordinary Tortrix or Gelechia.

1. Forewings with costal half yellow chrysitis.
" " " not yellow 2.
2. Forewings obliquely streaked with white and fuscous 3.
Forewings not obliquely streaked with white and fuscous 4.
3. Palpi wholly white leucocyma.
" with two black rings aëllomacha.
4. Palpi with two black rings æthalota.
" without two black rings 5.
5. Palpi with second joint whitish linearis.
" " reddish-ochreous chalcodelta.
– 183 –

§ A. Vein 7 of hindwings from angle of cell.

42. Grac. chrysitis, Feld.

(Gracilaria chrysitis, Feld., pl. cxl.; G. adelina, Meyr., “Proc. Linn. Soc. N.S.W.,” 1880, 142; G. rutilans, Butl., “Cist. Ent.,” ii., 561.)

♂ ♀. 12–13mm. Head and thorax deep reddish-ochreous, violet-shining, face snow-white. Palpi reddish-ochreous, towards base white, terminal joint dark purplish-fuscous. Forewings deep reddish-ochreous, with coppery-violet reflections; a very broad pale metallic yellow costal band, its lower edge indented by a conical projection of ground-colour before middle, and a shorter one midway between this and base, both suffused with deep cobalt-blue; dorsal reddish-ochreous area marked on lower ⅔ with regular transverse strigulæ of deep cobalt-blue, appearing black in some lights. Hindwings rather dark grey.

Hamilton, Palmerston, and Christchurch; rather common amongst forest, in September, January, and March. This and the next two species are nearly related together.

43. Grac. chalcodelta, n. sp.

♂ ♀. 11–13mm. Head whitish-yellowish, more or less reddish-ochreous on crown. Palpi reddish-ochreous mixed with dark fuscous. Antennæ dark fuscous, ringed with whitish. Thorax reddish-ochreous. Abdomen whitish-grey. Legs purple-blackish, banded with white, middle tibiæ with large tuft of rough scales beneath, posterior tibiæ white. Forewings elongate, very narrow, long-pointed; reddish-ochreous, with purple gloss, with scattered blackish and yellow-whitish scales forming indications of obscure transverse strigulæ; costa and inner margin distinctly strigulated with black and pale yellowish; a pale brassy-yellow well-defined triangular patch on costa before middle, reaching about half across wing: cilia light grey, on costa and round apex reddish-ochreous, round apex mixed with blackish in several ill-defined lines. Hindwings and cilia light grey.

Whangarei, Auckland, Taranaki, Makatoku, Masterton; in December, February, and March, six specimens.

44. Grac. linearis, Butl.
(Gracilaria linearis, Butl., “Proc. Zool. Soc. Lond.,” 1877, 406, pl. xliii., 16.)

♂ ♀. 13–14mm. Head and thorax reddish-ochreous, sometimes with a brassy gloss. Palpi whitish, terminal joint dark reddish-fuscous. Antennæ fuscous annulated with whitish. Abdomen ochreous-whitish or grey. Legs dark purplish-fuscous, banded with white, posterior tibiæ white. Forewings elongate, very narrow, long-pointed; more or less deep reddish-ochreous, with a brassy gloss; a hardly perceptibly paler

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triangular patch on costa before middle; some scattered irregular blackish dots, mostly on posterior ⅔ of fold, and in a longitudinal series in posterior half of disc: cilia light grey or ochreous-grey-whitish, round apex and on costa reddish-ochreous. Hindwings and cilia grey or ochreous-grey-whitish.

Var. a. Forewings suffused with dark purplish - fuscous, with a bright reddish-ochreous streak along inner margin.

Larva 14-legged, moderate, cylindrical, tapering at both ends; dull grey-greenish or grey-yellowish; dorsal darker; subdorsal broad, grey, or obsolete; head and plate on second segment dark fuscous. Feeds between spun-together shoots or leaves of Coriaria ruscifolia, C. thymifolia, and C. angustissima, in January.

Napier, Wellington, Arthur's Pass (3,000ft.), Christchurch, and Invercargill; from December to February, common. I bred the species in abundance from the larvæ; otherwise I could scarcely have credited the unusual larval habit.

45. Grac. leucocyma, n. sp.

♀. 9mm. Head and palpi white. Antennæ fuscous, beneath white. Thorax light grey. Abdomen whitish. Legs dark grey, ringed with white, posterior tibiæ white. Forewings elongate, very narrow, pointed; grey; markings snow-white; a rather broad irregular streak along inner margin from base to apex, interrupted before middle by a very oblique indistinct line of ground-colour; eight short more or less wedge-shaped streaks from costa, first from ¼, slenderly produced on costa towards base, first four outwardly oblique, remainder inwardly oblique, second and fourth reaching half across wing, the rest mach shorter; a small irregular blackish apical dot, preceded by a white dot: cilia ochreous-grey-whitish, round apex whiter, with indications of two dark fuscous lines. Hindwings whitish-grey; cilia ochreous-grey-whitish.

Auckland, in December; one specimen. Although superficially resembling the following species, it is not really closely allied.

§ B. Vein 7 of hindwings out of 6.

46. Grac. aëllomacha, Meyr.
(Gracilaria aëllomacha, Meyr., “Proc. Linn. Soc. N.S.W.,” 1880, 158.)

♂ ♀. 7–9mm. Head and palpi snow-white, palpi with apex of second joint and a subapical ring of terminal joint black. Thorax snow-white, with a small black spot on shoulder. Forewings snow-white; markings fuscous, irrorated with dark fuscous; a cloudy central longitudinal streak from near base to disc above anal angle, more or less obsolete towards base, connecting obscurely with about seven oblique

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costal and about four oblique dorsal streaks (these vary somewhat); costal streaks usually alternately slender and thick; a fuscous apical spot: cilia grey, round apex white, with two dark fuscous lines and a black apical hook. Hindwings fuscous-grey, cilia paler.

Wellington and Christchurch, in September, January, and February; four specimens.

47. Grac. æthalota, Meyr.

(Gracilaria æthalota, Meyr., “Proc. Linn. Soc. N.S.W.,” 1880, 143.)

♂. 9mm. Head and thorax fuscous-grey, face grey-whitish. Palpi whitish, apex of second joint and a subapical ring of terminal joint black. Forewings purplish-grey; margins faintly dotted with ochreous-whitish posteriorly: cilia grey, with obscure darker lines, and a white apical hook. Hind-wings fuscous-grey, cilia paler.

Dunedin, in January; one specimen. Notwithstanding the different superficial appearance, this species is nearly allied to the preceding.

Coriscium, Z.

Characters of Gracilaria, but palpi with a loose projecting tuft of scales towards apex of second joint beneath, terminal joint usually longer than second.

48. Cor. miniellum, Feld.

(Coriscium miniellum, Feld., pl. cxl.; Gracilaria ethela, Meyr., “Proc. Linn. Soc. N.S.W.,” 1880, 152.)

♂ ♀. 11–13mm. Head yellow on crown, crimson behind, face snow-white with two pale crimson spots. Palpi white, second joint crimson. Thorax yellow, anterior margin and a posterior spot crimson. Forewings pale yellow, deeper towards inner margin; a bright crimson undulating central streak from base to apex, sometimes margined with dark fuscous above, connected with inner margin by perpendicular bars near base and at ¼, ½, and ¾, and connected with costa at and near base; a round crimson apical spot, containing a blackish spot towards costa, and a white triangular spot on inner margin: cilia yellow round apex, with a dark fuscous hook, crimson below apical spot, thence very pale crimson. Hindwings light crimson, cilia very pale crimson, on costa grey.

Var. a. All crimson colouring replaced by ochreous-brown, margined with dark fuscous.

Hamilton, Taranaki, and Palmerston; from January to March, locally plentiful, frequenting the depths of the forest. The variety occurs with the type, but much more scantily, in the proportion of about one in fifteen. I can offer no explanation of the magnificent colouring of this species, which would

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be extraordinary anywhere, but is singularly different from the usually sombre insects of New Zealand.

Conopomorpha, Meyr.

Vein 11 of forewings should have been given as present, from near base of cell. The generic characters have been given previously, and need not be repeated. The genus is distinguished from Gracilaria by the rough hairs of posterior tibiæ, the rough scaling of palpi, and the stalking of veins 3 and 4 of forewings.

49. Con. cyanospila, Meyr.

(Conopomorpha cyanospila, Meyr., “Trans. N.Z.Inst.,” 1885, 183.)

I need not repeat here the details given under the above reference, to which I have nothing to add.

Nepticulidæ.

Head rough-haired all over. Antennæ shorter than forewings, basal joint dilated to form an eyecap. Maxillary palpi developed. Hindwings lanceolate, cell open.

Probably this family should be included in the Tineidæ, to which it is closely allied, and from which it differs essentially only by the eyecap of the antennæ, not a very important point. At present I place them separate, until further consideration. The neuration of the known genera is of a very degraded type, and the species are amongst the smallest known Lepidoptera.

Nepticula, Z.

Head densely rough-haired; no ocelli; tongue absent. Antennæ ⅔–¾, in male simple, filiform, basal joint dilated and excavated beneath to form an eyecap. Labial palpi short, porrected, filiform or loosely scaled. Maxillary palpi moderately long, folded, filiform. Posterior tibiæ clothed with rough hairs above. Forewings with vein 1 obsoletely furcate, cell open between 2 and 6, 3, 4, 5 absent, 8 out of 7 or absent, 7 to costa, 9 absent, 11 from before middle. Hindwings ½–¾, lanceolate, cilia 3–4; veins 3, 4, 5 absent, cell open between 2 and 6, 6 and 7 apparently from a point.

The genus is probably cosmopolitan. In Europe and North America it is extensively developed, and I am acquainted with about twenty Australian species, some of which are very similar to the European. The larvæ have 18 rudimentary legs, and mine blotches or galleries in leaves; the Australian larvæ have the same habits as the European, but I have not observed signs of the larvæ in New Zealand. I have not properly examined the neuration of the following species, owing to the small size of the insects and the possession of only single specimens, but it appears normal.

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1. Forewings with ground-colour whitish-ochreous propalæa.
" " " pale grey 2.
2. Forewings with a pale suffused spot on costa posteriorly ogygia.
" without pale spots tricentra.

50. Nept. tricentra, n. sp.

♀. 6mm. Head and palpi grey-whitish. Antennæ, thorax, and abdomen grey. Legs dark grey, apex of joints whitish. Forewings lanceolate; pale grey, irrorated with darker; two or three small round black dots in an irregular longitudinal series towards middle of disc: cilia light grey. Hindwings and cilia light grey.

Christchurch, in March; one specimen.

51. Nept. ogygia, n. sp.

♂. 7mm. Head and palpi pale whitish-ochreous. Antennæ grey. Thorax and abdomen grey, sprinkled with ochreous-whitish. Legs dark grey, apex of joints whitish. Forewings lanceolate; pale grey, coarsely irrorated with black; an obscure cloudy ochreous-whitish suffusion towards costa at ⅔; an obscurely-indicated pale spot in disc before middle: cilia whitish-ochreous-grey, with an obscure line of dark scales round apex. Hindwings and cilia light grey.

Dunedin, in January; one specimen.

52. Nept. propalæa, n. sp.

♀. 7mm. Head, palpi, antennæ, and thorax whitish-ochreous. Abdomen light grey. Legs whitish-ochreous, anterior pair infuscated. Forewings lanceolate; whitish-ochreous, obscurely irrorated with brownish; a dark fuscous dot on fold at ¼, a second in disc before middle, and a third immediately before apex: cilia whitish-ochreous. Hindwings light grey; cilia whitish-ochreous-grey.

Arthur's Pass (3,000ft.), in January; one specimen.

The following additional notes on described species are made from specimens and information kindly sent to me by Mr. G. V. Hudson:-

Sceliodes cordalis, Dbld. Bred by Mr. Hudson from larvæ feeding in the berries of Solanum aviculare. This is a very interesting observation: the insect occurs in Celebes and Australia as well as in New Zealand, and its attachment to the widely-distributed genus Solanum explains the possibility of this.

Œcophora scholæa, Meyr. Bred by Mr. Hudson from a larva living in a silken tube underground beneath the roots of an old tree.

Œcophora politis, Meyr. Mr. Hudson informs me that this species rapidly becomes worn, and is difficult to obtain in

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good condition; but he has sent me a fresh female, from which it is evident that the specimen I originally described is so much bleached that the description can hardly be applied to the fresh insect: I therefore redescribe it.

♀. 18–21mm. Head ochreous-yellowish. Palpi pale yellowish, second joint irrorated with fuscous on lower half. Antennæ fuscous. Thorax fuscous, apex of patagia and a posterior spot yellowish. Abdomen grey. Legs grey, posterior pair whitish-yellowish. Forewings elongate, slightly dilated, costa gently arched, apex round-pointed, hindmargin rather strongly oblique, slightly rounded; pale ochreous-yellowish, suffused with reddish-fuscous except towards costa anteriorly; a moderate well-defined clear ochreous-yellowish streak along inner margin from base to near anal angle, attenuated posteriorly, its upper margin triangularly indented before middle and edged by a darker reddish-fuscous suffusion; an obscure darker dot in disc at ⅖, and a second at ⅗, connected by an obscure pale line; faint indications of an angulated posterior darker line, indented above middle: cilia reddish-fuscous, irrorated with yellow-whitish. Hindwings and cilia grey.

It would not surprise me much to find that this was the other sex of Œc. phegophylla.

Mecyna deprivalis, Walk. I found the larva of this species commonly near Nelson, feeding on Sophthora (Leguminosæ), and give the description in full detail, to allow of comparison with the larvæ of closely-allied exotic species. Larva 16-legged, elongate, cylindrical, slightly tapering towards ends, with very long scattered whitish hairs; dull light bluish-green, segmental incisions more yellowish; an irregular raised white line above spiracles, becoming yellowish towards incisions, and obscurely margined with yellowish elsewhere above; segments 3–4 with one, 5–12 with two large raised black spots on each side of back, each spot marked with a white dot on each side, posterior spot of 12th segment white, black-centred and with a black rim; beneath anterior of these spots a large raised black spot on each segment; beneath this on segments 3–4 two moderate raised black spots, on segments 5–12 a black dot surrounded with whitish; on 12th segment a black dot on supraspiracular line, beneath which is another black dot surrounded with whitish, and enclosed beneath by a semicircular black rim; spiracles black, surrounded by a circular whitish spot enclosed with a black rim; head testaceous; second segment grey-whitish, irregularly streaked and spotted with black; anal segment grey-whitish, dotted with black.

This larva is therefore conspicuously distinct from that of the Australian M. polygonalis.

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Art. XV.—On the Natural History of three Species of Micro-Lepidoptera.

[Read before the Wellington Philosophical Society, 25th July, 1888.]

Plate VIII.

In most of the openings in the bush round Wellington may be seen a conspicuous-looking shrub, with very dark-green leaves and purple flowers, which in the autumn are replaced by large quantities of bright orange-coloured berries. Its popular name is, I believe, the New Zealand night-shade, and it is scientifically known as Solanum aviculare. About January a large number of these berries are full grown, although as yet quite green and unripe. It is in these that we must look for the larva of Sceliodes cordalis, Dbld., one of our most beautiful Pyrales, whose presence is readily detected by the large holes which it drills in the sides of the berries. When extracted from its burrow, this caterpillar is found to be very robust and of a light-reddish colour, paler beneath (pl. viii., fig. 2). Like most internal-feeding larvæ it is very sluggish, and seems quite helpless in the open.

The infected berries can easily be placed in a caterpillarcage, and the enclosed larvæ will emerge when they are full grown and spin their small white cocoons on the sides of the cage, in which they are transformed into pupæ, the moths appearing about a month later.

This species is very partial to light, and hence frequently enters houses, but the best and most interesting method of procuring it is to rear it from the berries.

Our next species (Heliostibes atychioides, Meyr.) belongs to the Tinidæ, and its larva is found on the manuka (Lepto-spermum), twisting up the terminal shoots and devouring the leaves. It lives in a kind of tube which runs along one of the twigs, and is constructed of a mixture of leaves and silk. In colour this larva is dark brown, with the head and two first segments corneous, the rest of the body being ornamented with two black spots on the sides of each segment. The subdorsal and lateral lines are whitish, the former with an interrupted central black line (fig. 4). These caterpillars are rather difficult to extract from their habitations, as they are extremely active, darting either backwards or forwards with equal rapidity whichever end we happen to attack. When full grown, the insect closes up both ends of its tube, and constructs a small cocoon within, where it changes into a pupa from which the moth emerges in about three weeks' time, when it may be seen in great abundance, flying round the

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manuka bushes towards evening during December and January. Specimens for the cabinet should always be reared from the larva, as the extreme activity of the perfect insect causes those captured in the open to be nearly always more or less injured (fig. 3).

Another species of Tortricidæ attached to the manuka is Cacæcia excessana, Walker. Its larva is very different from that of the preceding species, being of a light-green colour with a conspicuous yellow lateral line (fig. 6). During the spring months it joins one or two leaves together, feeding within, and is very active, leaving its retreat immediately when detected and lowering itself by a silken thread to the ground. The pupa is enclosed in a slight silken cocoon between two manuka leaves, and the moth appears about the end of November (fig. 5).

Description of Plate VIII.

Fig. 1. Sceliodes cordalis.

Fig. 2. " larva.

Fig. 3. Heliostibes atychioides.

Fig. 4. " larva.

Fig. 5. Cacæcia excessana.

Fig. 6. " larva.

Art. XVI.—On the Varieties of a common Moth (Declana floccosa).

[Read before the Wellington Philosophical Society, 13th June, 1888.]

Plate IX.

Seeing that the variation of Lepidoptera is attracting so much attention in England at the present time, more especially in its relation to the origin of species, it occurred to me that perhaps a few remarks on one of our moths (Declana floccosa) might be of some interest, especially as it seems not unlikely that we are here actually witnessing the gradual evolution of several distinct species from a single one of a very unstable character. I must, however, begin my remarks by stating that my information on the subject is at present very limited, the varieties of this insect which actually exist being doubtlessly very much more numerous than those which I have here figured and described. My chief object in writing this paper is not so much to give information, as to arouse a more active interest in a subject which I feel is far too comprehensive to be dealt with by myself alone.

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To illustrate Paper by G.V.Hudson.

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With respect to the normal type of Declana floccosa, it is extremely hard to say much, as the several varieties do not contain any characters common to all of them, although, in many instances, the same markings can be recognised in several different forms. Thus we have nothing definite which can be said to form the basis of the species; our only course, therefore, is to take the simplest form, and regard that as the type. Pl. ix., figs. 7 and 8, represent this form. The following is a brief description: Front wings pale greyish white covered with numerous brownish-black streaks, exhibiting a slight concentration towards the tip of the wing, but varying much in intensity (compare figs. 7 and 8). Hindwings buff-coloured, shaded with pale brown towards their exterior margins. Next in order to this most simple form is the variety depicted at fig. 1, which exhibits several large round spots on the disc of the front wing, the minute streaks being decidedly concentrated on the hindmargin, and leaving the central portion of the wing considerably paler in colour than in the usual type. From this form we will now pass to an insect which was long known as Declana nigrosparsa, from the numerous black spots ornamenting its frontwings. It is a tolerably common and easily recognised variety (fig. 4).

Pl. ix., fig. 2, represents another very characteristic form of D. floccosa, distinguished from the type by the two conspicuous stripes which cross the forewings from the costa to the inner margin; one being situated near the thorax, and the other at about two-thirds of the distance towards the hindmargin, this latter being doubly curved. A further development of this form is drawn at fig. 5, where these two stripes are joined together, near the middle, by two lines running parallel with the hindmargin and costa of the wing. These two varieties were described under the name of Declana junctilinea, Mr. Meyrick having subsequently shown in his paper on the New Zealand Geometrina,* that they were inadmissible as species. A form combining the characters of nigrosparsa and junctilinea is shown at fig. 3, where we have both the curved lines and numerous black spots. Finally, we have a most conspicuous form (fig. 6), showing the greatest deviation from the original type, where the frontwings are entirely suffused with dark greyish-black, except two broad bands of the original light colour extending from the costa to the inner margin. The base and hindmargin of the posterior wings are also much suffused with dark-grey, leaving a broad ill-defined band of lighter colour across the middle of the wing.

Taking now a general view of these varieties it is manifestly impossible to regard them as constituting more than a

[Footnote] *“Trans. N.Z. Inst.,” vol. xvi., p. 49.

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single species, the numerous intermediate forms between the most marked of them rendering any attempts at subdivision completely futile. At the same time, I am led to believe that the larvæ of two of the most distinct types of variation—namely, nigrosparsa and junctilinea, exhibit considerable differences, although I have not yet reared a sufficient number to form any decided opinion on the subject. The larvæ of figs. 1, 4, 7, and 8, including the type and two varieties, feed on the New Zealand “currant” or “wineberry” (Aristotelia racemosa), and are of a dark reddish-brown colour, sometimes marbled with grey, closely resembling the twigs of the trees, and thus affording the caterpillars the usual protection from enemies. On the other hand, the larvæ of the vars. figs. 2 and 5 are light yellowish-brown with irregular darker markings, approximating closely to the stems of the manuka (Leptospermum), on which I have always found them. To any one interested in the development of species and inheritance of parental peculiarities, I think that this insect would be a most useful object for investigation. The fact that none of the varieties I have mentioned are confined to any particular sex would be most advantageous, as the experimentor could readily select a male and female of each conspicuous form from which he could obtain ova, and thus ascertain whether the well-marked peculiarities of the parents were inherited, or, in other words, whether there was any tendency to establish a permanent or specific character. Should it be found feasible to carry the observations through several generations of moths, I feel sure that the result obtained would have an important bearing on that much-vexed question, the origin of species.

Before concluding, I should like to point out how eminently suitable insects are for investigations of this character. In the first place their brief life enables the industrious observer to watch the same family of insects for several generations, an impossibility in the case of most other animals, while the conspicuous characters which distinguish the majority of the species, especially of the Lepidoptera, render any departure from the normal type at once perceptible. It is consequently somewhat surprising that they have been so little made use of, and it can only be attributed to that prejudice which unfortunately exists against the study of entomology even in the present day. Workers in most of the other branches of science are allowed to push their investigations far beyond the limits of direct usefulness, and are encouraged for their zeal and perseverance in so doing, whereas, in the case of the entomologist, unless the insects he is investigating are connected with agriculture or some other matter of equal importance, his labours are regarded as a mere waste of time. With respect to this idea, I can only say that, if the same utilitarian argu-

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Declana Floccosa. Vate.

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ment, which is applied so unsparingly to the entomologist, was used in every instance, I think that we should soon find that the majority of our most cherished studies and recreations might be readily dispensed with, and our lives consequently reduced to a condition of miserable monotony.

In England, I am happy to say, entomology is being more appreciated every day, the number of entomologists having increased enormously during the last twenty years. The Entomological Society of London alone consists of over three hundred members, while there are at least three other larger societies in London devoted almost exclusively to the same science. Surely a few inquiring minds in New Zealand will turn their attention to a study which offers a boundless field for investigation, coupled with inexpensiveness and plenty of out-of-door recreation.

Description of Plate IX.

Figs. 1–8. Varieties of Declana floccosa.

Art. XVII.—A Description of a new and large Species of Orthopterous Insect of the Genus Hemideina, Walker.

[Read before the Hawke's Bay Philosophical Institute, 12th Nov. 1888.]

Insecta.
Order. Orthoptera.
Section. Saltatoria.
Fam. Locustidæ.

Genus Hemideina.

1. H. nitens, sp. nov., Col.

Female.—Piceous slightly convex, very glossy. Head small, dark (almost black), smooth with a stout keel between the eyes which is forked between antennæ; eyes very prominent, almond-shaped broad end above horns; antennæ (tips broken off) 1¾in. long, sub-moniliform, thickly pubescent, less so at base; clypeus blackish with a transverse brown band; labrum brown; labium black; palpi brown, fifth joint pubescent (also fourth, but less so), tip oval-spathulate; labial palpi slightly hairy, tip broadly-oblong. Prothorax (thoracic shield) much curved, 8 lines long, 4 lines wide, sub-rugulose, margined, anterior margin minutely ciliate, tawny brown with deeply indented rather coarse black markings (somewhat like

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a broad full face with spreading horns); pronotum thickish; shield-like, margined, both it and mesothorax very dark; abdomen slightly compressed, clouded; abdominal segments darker below, increasing in hue towards tip; oviduct large, very thick at base; 10 lines long, curved, brown almost piceous. Legs stout; femora with 2 (sub 3) rows of black coarse oblong spots on each side; hind femora with a row of large black spines on lower margin (which is also black), and 2 minute ones inside of the row; the 4 anterior femora smooth; 4 anterior tibiæ with 5 black spines on each side; hind tibiæ very stout, black, with 4 long black spines on the outer side and 5 on the inner side, the third and fourth of the inner ones very long (⅛in.) and sharp, and 2 small spines distant on the upper ridge; the posterior femora and tibiæ of about equal length—11 lines long; the anterior tibiæ with a pair of spines at the lower joint, upper side; the middle tibiæ with a single spine there; the posterior tibiæ with 2 pairs of spines ditto; tarsi piceous, almost black, slightly hairy; hairs short, patent; pulvilli thick, tumid, blackish, shining. Length of body 16 lines.

Hab. Found in firewood obtained from Forty-mile Bush, County of Waipawa, 1888; per Mr. A. Hamilton.

Obs. A peculiar species, differing from other described ones in its general very dark colour, extreme glossiness, having also a sub-metallic cupreous glow in several places, peculiar broad and coarse femoral markings, extra spines, remarkably thick and smooth tumid pulvilli, and hairy antennæ. I regret much the upper portions of the antennæ being wanting.

Art. XVIII.—Notes on a peculiar Chrysalis of an unknown Species of Butterfly.

[Read before the Hawke's Bay Philosophical Institute, 8th October, 1888.]

Lepidoptera.
Section Rhopalocera.
Fam. Nymphalidæ.

In the summer of 1887 (February), while botanising in the secluded forests and glens south of Dannevirke, I came upon a curious living chrysalis of a form hitherto unnoticed by me. It was attached to a branch of a species of Galium,* a large

[Footnote] * Galium triloba, Col., sp. nov., “Trans. N.Z. Institute,” vol. xx., p. 192. (I have since detected this curious species growing profusely prostrate in large beds.)

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prostrate plant, and, believing it to be new, I carefully secured it and brought it to Napier. As I expected it would shortly emerge in its imago state, I took accurate notes of this chrysalis in its fresh and living state, also a drawing of it, which I now give. I failed, however, in seeing the perfect insect, as the chrysalis never developed, but lost its original colours and decayed. I suppose it must have received some bruising in carriage, &c., although I took every possible care, having also formerly reared perfect insects of Pyrameis gonerilla, Danais berenice, Dasypoda selenophora, and others. It may be, however, only the pupa state of one of our known New Zealand butterflies, and also known to our colonial lepidopterists, who will in that case immediately recognise it from my description. It was certainly both very peculiar in shape and richly adorned in colours.

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[The section below cannot be correctly rendered as it contains complex formatting. See the image of the page for a more accurate rendering.]

1. Side view. 2. Front view. Chrysalis 10/12 inch long; slightly enlarged.

Description.—Chrysalis: Suspended by a stout web from its tail (none around the body), oblong (outline form), 10 lines long, 4 lines broad; somewhat sub-angular and rough, with many small muricate projections; colour olivaceous, smooth yet finely corrugated, glossy, with minute short wavy transverse black veins; the thorax and head having a semi-metallic glistening appearance, as if finely powdered with gold dust, with 6–8 large and more defined bright gold-like round spots on underside of thorax and head. Head broad, truncate and retuse almost bifid, acutely 2-horned at outer angles; sternum largely produced and very acute; tail produced, tip blackish, ½ line long, curved with a stout silken band 3 lines long; back flattish, with 4 small sharp points (2 pairs) near the centre and 2 larger on each side (edge of wings) nearly in the same lateral line, and 1 smaller on edge near fourth abdominal ring, and 5 blackish spiracle-like slits in a curved line from fourth abdominal ring to tip of tail; several fine longitudinal black lines running from each side of horn to the fifth and largest ring of abdomen, the outer pair of lines regularly studded their whole length with minute raised points; 3 large posterior black rings and 4 sub-obsolete anterior ones on abdomen underside; 8 pairs of acute points (feet) in 2 longitudinal lines, with 6 smaller central ones in a longitudinal line on abdominal rings; and a shining blackish disc with raised margin in centre of thorax under sternum.

Obs. This chrysalis somewhat resembles in form that of Vanessa io. Viewed in front its prominent sternum, &c., bears a likeness of the human face in ludicrous miniature. I

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have ventured to classify it under the family of Nymphalidæ, from the fact of its only suspending itself by its tail. I am aware that the sub-family of Libythæinæ (Fam. Erycinidæ) does the same, but hitherto (as far as I know) none of this sub-family has been found in New Zealand.

Should any of our colonial lepidopterists, who may see this notice, be already acquainted with this form of pupa, and also with its perfect insect, I will thank him to inform me of it.

Art. XIX.—A few Notes on the Economy and Habits of one of our largest and handsomest New Zealand Butterflies (Pyrameis gonerilla).

[Read before the Hawke's Bay Philosophical Institute, 8th October, 1888.]

A Few years ago, during my visits to our inland forests, I often had to pass close to a large shrubby Urtica,* and I invariably saw several of our large and handsome butterfly, Pyrameis gonerilla, hovering over it or settled on it. The shrub itself was in a sheltered sunny nook; and on one day in particular in early spring I counted no less than seventeen of these beautiful creatures at one time so engaged about that shrub, which none of them seemed desirous of leaving. It was a truly lovely scene which I well remember. Spring's woodland harbinger, the large-flowered clematis (C. indivisa) was pretty well-developed overhead, swinging and displaying its long wreaths of peerless and pendulous virgin-white tresses from the lofty trees up which it had climbed when young; around were the many beautiful and stately tree-ferns, while below the ground was thickly carpeted with that neat close-growing bedding plant, with small and regularly - formed emerald foliage, Pratia angulata, expanding thankfully its myriads of white and blue star-like blossoms to the morning sun, and so drinking in life. The sun, too, was shining brightly down from the deep concave of the dark-blue sky, rarely flecked by a passing cloud; while the melodious tuis (Prosthemadera novæ-zealandiæ—parson-bird of the colonists), having had their breakfast of honey and nectar, were singing away joyfully and with good courage from their tiptop perches on the highest sprays, their dark and lustrous metallic plumage reflecting the rays of the sun. It is worthy of notice that this handsome and highly melodious bird always selects the highest and bare spray of a tall tree for its music-stool,

[Footnote] * U. ferox, Forst., or a closely allied and undescribed species: U. pungens, MSS.

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whence to pour forth its gushing notes; and this habit is more particularly observed by them soon after sunrise and at sunset, when to hear them of a fine summer's evening, when all is calm above and still below, is really ravishing. At such times the song by Capern, called “The Old Grey Thrush,” has come forcibly to mind. As some of you may not know it, permit me to give part of the first stanza:—

Of all the birds of tuneful note
That warble o'er field and flood,
O, give me the thrush with the speckled throat,
The king of the singing wood!
For see, he sits on the topmost twig
To carol forth his glee,
And none can dance a merrier jig,
Or laugh more loud than he.

The whole of that song is apt (for the tui), and well worth repeating. To return, however:—altogether it was a pleasant time; all nature seemed in harmony; even the murmur of the rippling waters of the neighbouring brawling stream joined in unison, and conveyed a more soothing cadence than usual to the ear; and the briskly flitting butterflies above all appeared to be revelling in luxury, enjoying themselves and making the most of it. At such seasons snatches from the once popular song of fifty or sixty years ago, and long forgotten, “I'd be a butterfly, born in a bower,” &c., would come rushing rapidly along through the dark lanes of encumbered memory into broad daylight. I remember well, standing entranced, as it were, for several minutes, contemplating and admiring the scene before me ere I could bring myself to resume my journey, and dive into the deeper and gloomy recesses of the forest.

That is a faint and brief description of what I saw there at that grand butterflies' ball and feast, in the early spring.

On a subsequent visit to that spot, one day in the autumn (28th April), on examining the Urtica shrub, I found 3 larvæ and 2 chrysalides of the Pyrameis on it: the larvæ feeding on its leaves, the pupæ hanging from it. The pupæ were suspended by a few tiny threads under a leaf, or within a leaf (or sometimes two leaves), the edges being very slightly drawn together with threads, but not closed up, remaining more than half open. In taking these rudimental insects, and gathering some of the leaves of the Urtica for the larvæ to feed on, I somehow got stung rather severely, in spite of all my care. I well remember the sharp permanent pain from the sting of that nettle, which lasted four days,* and was always increased through washing or wetting my hands.

[Footnote] * Since writing the above I find the same fact already recorded—“Fl. N.Z.,” vol. i., p. 225, and “Handbook Fl. N.Z.,” p. 252—I having forty years before experienced the same discomfort.

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Four days after I again visited that spot and Urtica shrub for the last time that season (as I was to return to Napier the next day), and found 3 more larvæ and 2 chrysalides, and brought them all away. Arriving at Napier on the 2nd May, I placed the larvæ, with a quantity of fresh leaves, in a large white glass bottle; on the 4th, one of the larvæ had suspended itself to the (bored) cork of the bottle; on the 6th it cast its larva-skin and partly took up the chrysalis appearance, but was very wet at first; and on the 7th it assumed the true chrysalis aspect. On the 9th another of the larvæ hung itself to the cork, head downwards, and commenced its transformation. On the 11th one of the chrysalides dropped off from the cork; I had noticed that this one was smaller and of a lighter colour. On the 18th another of the larvæ entered into its chrysalis state, also attaching itself to the cork of the bottle.

On the 19th one of the chrysalides I had brought in that state from the forest burst, and the perfect insect emerged; but, owing to the shallowness of the glass in which these forest chrysalides were confined, one wing had got stuck fast to the side of the bottle in the process of emerging, and so became contracted and rigid when dry, like a little plaited epaulette; while the other wing, being free, had attained to its full size and shape; but the poor creature was sadly lopsided. On the 21st another of the forest chrysalides split open, and the imago emerged—a beautiful sight,* once seen, never to be forgotten.

A thing of beauty is a joy for ever.

This was a fine and perfect specimen of this butterfly.

I regretted much those larvæ that entered into their pupa state here in Napier not emerging therefrom as perfect insects. I suspect this was owing either to their not having been fully fed down to the time of their entering into that state, or that they assumed it too early, and perhaps in an unhealthy state. As larvæ they were very voracious; it seemed as if they were always eating, night and day; so that my stock of Urtica leaves that had cost me so dearly were soon disposed of. On their being used up I tried the hungry creatures with several other leaves of Maori plants, but none would they touch. That shrub itself, though a large bushy and spreading one (about 5ft. high and several feet round), with several others, smaller ones, close by, almost always presented a sorry sight from their leaves being so gnawed and stripped; hence I had always some difficulty in procuring good specimens of it for drying and preserving. Those Urtica plants, however, recovered themselves throughout the winter, and were fully

[Footnote] * See the full description of similar emergence of Danais berenice, as witnessed by me (“Trans. N.Z. Inst.,” vol. x., p. 279).

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foliaged in early spring. I may also mention that, though the plant was said to be well known in that locality, I only met with it in one other spot, and that a single small specimen.

Seeing that the larvæ in their purely natural state always either suspend themselves to a twig or enwrap themselves in a leaf of the Urtica, it seemed strange that in no case did one of them so suspend itself to a stem in the bottle, but only and always to the cork (of course there were no leaves left). Was this done on account of more moving air there through the holes—such being requisite to dry their wings quickly when emerging—or to be in a position of more free space?

As I suppose both larva and pupa of this butterfly to be, like the perfect insect, well known, I do not attempt to describe them. The larva is a curious-looking object, from its being so very hairy; the hairs, too, are rather long, rigid, patent, dark-coloured, and produced in little bunches of irregular lengths.

Notwithstanding my partial failure in the rearing of them, a few plain facts in the natural economy of this butterfly seem to be substantiated: (1) That its larvæ feed on the leaves of Urtica ?pungens, Col., and are very voracious; (2) that on their entering into the chrysalis state they wrap themselves loosely in a leaf of the same plant, to which they are also fastened, or suspend beneath a leaf from its petiole or branchlet; (3) that the time occupied by the embryo insect in its chrysalis state is more than three weeks; (4) and that if it has not ample room for unfolding its wings on emerging from the chrysalis state they become stunted and useless, and then of course the insect is destitute of flight.

Addendum.

I may here mention a similar case, as to contraction of wings under similar circumstances, that occurred a few years ago. In 1884, in a case of apples received from America (? California), I found a fine butterfly; one quite as large as our New Zealand Pyrameis gonerilla, if not much larger. It was but recently dead, and had evidently died in the case during the voyage; both of its wings were much crumpled and contracted, and its back chafed. Its prevailing colours were yellow and black (bluish-black) in broad streaks, the body the same, with broad yellow longitudinal stripes; very hairy at edges of wings in some parts; hairs long, yellow; and two large red spots on the wings; antennæ very dark, slender, naked; tips slightly clubbed; eyes very large and prominent. Being much crumpled, an only specimen, and tender, I only give its more striking aspect, as it requires to be softened and carefully laid out, before a strictly accurate description could be given. It is wholly unknown to me.

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Art. XX.—A few stray Notes on the New Zealand Owl, Athene novæ-zealandiæ, Gml.—Ruru and Koukou of the Maoris, and Morepork of the Settlers.

[Read before the Hawke's Bay Philosophical Institute, 8th October, 1888.]

When he heard the owls at midnight
Hooting, laughing in the forest,
“What is that?” he cried in terror;
“What is that,” he said, “Nokomis?”
And the good Nokomis answered:
“That is but the owl and owlet,
Talking in their native language,
Talking, scolding at each other.”
Hiawatha, Canto III.

Sevebal years ago—from 1844 to 1853—it was my lot to be often travelling on duty in the Wairarapa district. On one of those occasions I wished to reach the Maori village at the mouth of the Pahawa River on the east coast from the upper part of the Wairarapa Valley. In travelling thither we brought up for the night at the edge of a thicket, where my tent was pitched under a tree. My travelling companions and baggage-bearers, being weary with a long day's journey, were soon asleep, while I sat up reading, enjoying the stillness of the night, for it was a beautiful calm and moonlight one. Presently I heard a strange noise, or rather a succession of strange and peculiar unusual noises, such as I had never heard before. These were repeated over and over, in different and strange keys and semi-discordant tones, mixed with shrill hissing, and seemed as if coming from some creatures over my head; and at last, as I could not stand it any longer, I unlaced the door of my tent and got out. Keeping quiet, and concealing myself and looking up, I saw two owls on a rather bare extended horizontal branch of the tree only a few feet above me, and these were a pair, male and female, carrying on their courtship in the most strange manner imaginable. Such a grotesque sight I never saw before or since. The manner in which they acted; their pantomimic movements—half sedate and half funny—the gentleman owl advancing from his end of the branch with his head-feathers trimmed and set up cap-à-pie, and his wings let down, making with them a jarring noise as if he were a little turkey-cock, and at the same time uttering all manner of strange wooing sounds, high and low, short and long; and then the lady owl, on her part, retreating to the further end of the branch with measured step and slow, turning round, bridling herself up, hissing, and scornfully resenting the behaviour of the other; also, at times, uttering

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strange noises, and adjusting her feathers to suit her scornful affected prude demeanour. Then the disappointed beau would slowly retire, making other peculiar sounds, to his end of the branch; when the lady would again come forward, very slowly and coquettingly, to her old position, and in a short time the gentleman owl would re-enact the solemn fun as before, only to be again served in the same kind of way. Such a mixture of strange sounds and grimaces, of pure bird persiflage, was unique and unusual. Words fail me fully to describe them; it was most ludicrous to behold them. The usual solemn gravity of the bird seems to have been abandoned or burlesqued. I watched them for about half an hour, when, as their play was still being carried on without alteration, I returned to my tent. I could not help thinking, from observing the extreme suitableness of that long horizontal half-denuded branch, with its bunch of leafy sprays at both ends, for their wooing and serenading,—and bearing in mind how confined the owl naturally is in its short flights, and prone to return to its haunts and perches,—that that branch was used as an old trysting-place by owls. I did laugh most heartily, though quietly, at this serio-comic performance; and whenever I have thought thereon, during these many subsequent years, it has always caused me to laugh outright.

I dare say some of my audience are acquainted with that charming book of Natural History, Gilbert White's “History of Selborne,” so highly prized at home by our fathers. To those who know it, I need not say anything about it; but to those who do not, I would say—it is a most interesting book, written by an accomplished and loving naturalist, a keen and attentive observer of Nature in her manifold forms, but especially at home in his many and diverse observations on birds, as well as other animals: it is not a “dry” book. Mr. White was born at Selborne, in Hampshire, England, where, after his return from the University of Oxford, he quietly resided all his days, so spending an amiable, unambitious, and useful life, and died at an advanced age, much regretted. He steadily refused all church preferment, and during the last few years of his life officiated as curate of Selborne. His standard work has gone through several editions, and has always been highly esteemed by all lovers of Nature. Here I may be allowed to give a short sentence from its preface, written by himself exactly a hundred years ago (1788): “If the writer should at all appear to have induced any of his readers to pay a more ready attention to the wonders of the creation, too frequently overlooked as common occurrences, his purpose will be fully answered. But if he should not have been successful in any of these his intentions, yet there remains this consolation behind—that these his pursuits, by keeping

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the body and mind employed, have, under Providence, contributed to much health and cheerfulness of spirits, even to old age.”

Among his numerous scientific correspondents, one, who then stood prominently, was the celebrated working British naturalist Pennant, who was himself a correspondent of Linnæus. (Some of thé works of Pennant are on our libraryshelves: and his name is maintained and recorded among us in this country as that of a botanical genus, in our curious New Zealand forest-tree, Pennantia, so named by Forster.) And in an early letter from White to Pennant he makes a very similar complaint to that which I also drew your attention to in my “Presidential Address” four months ago. White says: “It has been my misfortune never to have had any neighbours whose studies have led them towards the pursuit of natural knowledge; so that, for want of a companion to quicken my industry and sharpen my attention, I have made but slender progress in a kind of information to which I have been attached from my childhood.”

To return. On this subject of the variations in the hooting of owls, White has some shrewd remarks, bearing, I think, on this part of owl-conduct I have just narrated; though it does not appear that White, or his correspondents, had known the reason or cause of the variations they had noticed in the owldialect. White says: “A friend remarks that most of his owls hoot in B flat; but that one went almost half a note below A. The pipe he tried their notes by was a common half-crown pitch-pipe, such as masters use for the tuning of harpsichords; it was the common London pitch.” And, again, White remarks: “A neighbour of mine, who is said to have a nice ear, remarks that the owls about this village hoot in three different keys—in G flat or F sharp, in B flat, and A flat. He heard two hooting to each other, the one in A flat and the other in B flat. Query: Do these different notes proceed from different species, or only from various individuals?” (loc. cit., pp. 234, 235.)

Other and very interesting remarks by White, on owls, are to be found in his letters. An extract from one in particular I will give you. It is contained in a letter to the Hon. Daines Barrington, whom you may remember hearing of as taking a long journey (in those days) to Mousehole, at the extreme end of Cornwall (close to my native place, and not far from the Land's End), to see and converse with the celebrated old fisherwoman, Dolly Pentreath—said to have been the last person who spoke the ancient Cornish language. White says: “We have had ever since I can remember a pair of white owls that constantly bred under the eaves of this church. As I have paid good attention to the manner of life of these

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birds during their season of breeding, which lasts the summer through, the following remarks may not be unacceptable: About an hour before sunset (for then the mice begin to run) they sally forth in quest of prey, and hunt all round the hedges of meadows and small enclosures for them, which seem to be their only food. In this irregular country we can stand on an eminence and see them beat the fields over like a setting-dog, and often drop down in the grass or corn. I have minuted these birds by my watch for an hour together, and have found that they return to their nest, the one or the other of them, about once in five minutes; reflecting at the same time on the adroitness that every animal is possessed of as far as regards the well-being of itself and offspring. But a piece of address, which they show when they return loaded, should not, I think, be passed over in silence. As they take their prey with their claws, so they carry it in their claws to their nest: but, as their feet are necessary in their ascent under the tiles, they constantly perch first on the roof of the chancel, and shift the mouse from their claws to their bill, that their feet may be at liberty to take hold of the plate on the wall as they are rising under the eaves… The plumage of the remiges of the wings of every species of owl that I have yet examined is remarkably soft and pliant. Perhaps it may be necessary that the wings of these birds should not make much resistance or rushing, that they may be enabled to steal through the air unheard upon a nimble and watchful quarry… When brown owls hoot their throats swell as big as a hen's egg. I have known an owl of this species live a full year without any water. Perhaps the case may be the same with all birds of prey. When owls fly they stretch out their legs behind them as a balance to their heavy heads; for as most nocturnal birds have large eyes and ears they must have large heads to contain them. Large eyes, I presume, are necessary to collect every ray of light, and large concave ears to command the smallest degree of sound or noise” (l.c., pp. 245, 246).

And all these apt quotations naturally bring me back to the main subject of this paper—our little New Zealand owl.

Probably none of you present have ever been in an unfrequented New Zealand forest many years ago—say, half a century, or forty years. Then those woods teemed with bird-life, so widely different to what has obtained of later years. Then our little New Zealand owl was to be often seen snugly ensconced in some sheltered umbrageous nook, and not unfrequently nestling close under the fronds of the tree-fern (Cyathea dealbata). There, for me, such would have ever remained unmolested, but not so by the smaller birds—denizens of the forest; for, as soon as his retreat

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was discovered by them, the battle, or rather the mobbing, began. The incessant noise the little fellows made brought up their friends from all quarters, and I have been sometimes astonished to see the great number—the cloud—of those small birds so quickly got together; and then, too, their apparent fearlessness or carelessness of my presence, of which they seemed to take no notice, so filled with rage were they and so very intent on insulting their common enemy. But while they would often fly up quite close to him, yet they never laid hold of him or touched him with their beaks; not a feather flew. Still the owl did not like it, and tried hard to get at them without removing from his perch, by thrusting forth his head and fiercely snapping his beak; and while I could see the difference in the dilation of the pupils of his eyes, which sometimes glared on the disturbers of his sleep and peace, yet I doubted if he clearly saw them, although he must have heard them plainly enough. I have never known the owl at such times to make any sound. Occasionally I have seen the so-persecuted bird fly away to some other neighbouring tree or bush; but in so doing he would generally make a woeful mistake, sometimes by coming abruptly against a branch, or between the close-growing canes of supplejacks (Rhipogonum), and sometimes by lighting in a less secure place, where the enemy could surround him, and then another fly-away would take place, and I have watched him to fly back to his old quarters; but it always seemed as if there would be no rest, no peace, for him while day-light lasted; and then, no doubt, the tables were turned upon his persecutors with heavy interest.

There being formerly no mice in this country, and I suppose our little New Zealand owl was far too diminutive to attack the now extinct New Zealand rat, and the small birds of the woods being then so exceedingly plentiful, these no doubt formed its chief articles of food, and this the little aerial legions well knew, and so naturally united to persecute him. I have good reasons, however, for knowing that some of our larger insects, especially of the Orthopterous order, as the big grasshoppers in the plains, and the wetas (Deinacrida and Hemideina) in the forests, formed a portion of the food of our owl; and now since mice have been introduced and become so numerous, and the indigenous small birds on the other hand have become so scarce, our owl does his share in the economy of nature to keep their number down, and therefore should never be wantonly destroyed as if he were an enemy and invader of the “rights of man.”

Before I close I would briefly refer to that exquisitely conceived and highly natural legendary fable of the ancient Maoris—viz., the great fixed “battle between the land and

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sea birds,”*—which has always served to remind me of Homer's battle between the frogs and mice—in which our little owl, who could not join the great united army of land birds in the long day's sanguinary conflict, owing to his being a nocturnal bird; yet, at the close of that prolonged fight, when the sea birds were utterly routed, distinguished himself by acting as a brave herald-trumpeter, and so added to their fear by joining in the pursuit with his insulting discordant note of ironical derision—toä koë! toä koë!—thou (art) brave! thou (art) victor! These words are ludicrously Maorified from the owls' common note of koū koū! koū koū! by a kind of onomatopeia—so common among the Maoris, and which a Maori, by a slight twist in the pronunciation, and more particularly when made in the mimicking tone, would cause them to pretty nearly resemble.

Having referred to that ancient Maori fable of the battle of the land and sea birds, in which nearly all our indigenous land birds are brought to the fore to repel the invaders, to fight and to perform prodigies of valour, even to the including of the piwakawaka, Rhipidura flabellifera, Gml.—the pied fantail-flycatcher—I would just call your attention to the grave fact of the total omission of the gigantic moa (Dinornis, sps.), and of all allusion to it, as a further proof of what some of you have already more than once heard from me, that the ancient Maori did not know of its living existence as a bird; for, if they did, they would have assuredly brought it prominently forward on that occasion as their great hero and redoubted champion, and the dreadful foe of the sea-birds, to whom, as giants in the battle-field, Goliath of Gath, or Og of Bashan, would have been but puny comparisons. That one plain and striking list of negative evidence, re the age in which the moa existed, has ever seemed to me to be of far greater value than all the loud and fussy statements of modern Maoris, made to suit the times and the wishes and questions of zealous European inquirers.

Art. XXI.—On the Birds of Lake Brunner District.

[Read before the Otago Institute, 10th July, 1888.]

Since the colonisation of New Zealand, less than forty years ago, the flora and fauna of some parts of the country have undergone many changes. This is most marked in the whole

[Footnote] * Translated briefly—together with some other of their ancient fables—by me, in Trans. N.Z. Inst., vol. xi., p. 102.

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country east of the central or dividing range, as it has been longer colonised and more adapted to agriculture and the depasturing of sheep and cattle than the bush lands west of the Alps. In the more settled or gold-mining centres of the west coast the same changes—disastrous to the flora and fauna alike—are now proceeding, but nowhere so rapidly as they have done on the east coast. A record of the modification and extinction among the fauna alone since the settlement of the colony would form a volume of great value. But as this is now impossible, it will be well to urge workers in all branches of zoology in New Zealand to collect all available material without delay, and record their researches from time to time. Following this method, I desire to place before this society tonight some observations on the ornithology of the Lake Brunner region of Grey County, West Coast. I am induced to offer a paper on the birds inhabiting the lake district, as the bush remains in its primeval state, and many of the anomalous and more specialised forms, formerly existing, but now extinct, east of the Alps, enjoy in it a fairly genial home. This, however, is destined soon to change, as the new Midland Railway when constructed will extend through part of the valley and near the shores of the lake for half its length. As the country becomes cleared and settled, only a few years will suffice to modify and extinguish much of the rich flora and fauna now existing in these beautiful and stern solitudes.

Very few writers on the zoology of New Zealand have dealt with this subject, yet the ordinary observer cannot fail to have detected the many changes proceeding continuously among various groups of animals. In the orders Lepidoptera, Cole-optera, Diptera, Orthoptera, and especially the Hymenoptera, a vast number of species have become locally extinct. Some are slowly diminishing, while others remain almost stationary, or continue to increase. In these several orders it will be found that the most specialised forms are the first to succumb. Although many have become locally extinct, or have been driven from their former haunts, some are still found where the features of the country remain unchanged, or the flora less modified. As the land is put under cultivation, or sheep and cattle are put to depasture on the native vegetation, the flora and fauna are soon more or less modified and become partly extinct.

There can be no doubt that the same causes affecting the extinction of our plants and insects can be shown to act in turn on the species of birds now fast dying out. The causes in New Zealand are clearing and cultivation, modification of climate, and the introduction of injurious and predatory forms. As many of our plants and insects are wholly dependent on each other for existence, any cause affecting the one affects the

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other. As the supply of insect-food lessens, some species of birds chiefly depending on it decrease according to the supply and rate of reduction. From peculiar habits in the economy of such species, they appear incapable of changing their food, habits, or environment, and ultimately become extinct. The extirpation of other species again is due to the ravages of introduced predaceous animals.

The cold winter of 1883, followed in the spring by severe late frosts, and the continuous cold wet summer of 1883–84, produced a wide-spread failure of the food of many species of birds. In the winter and spring followed the irruption of parakeets, extending over the whole of the east coast of the South Island, and the irruption or “plague” of rats on the west coast, which swarmed into some of the towns and villages. The tui and korimako left their home in the bush and migrated across the open country to procure food. All were in miserable condition and on the verge of starvation. They daily visited the flower-borders, and eagerly probed with their brushtongues the scarlet and yellow tube-flowers of Tritomia uvaria. The same season the wood-pigeon was miserably lean, being compelled to feed on the leaves of the kowhai and other trees, which cannot nourish and fatten like the fleshy nutritious-berries of the miro and others. The bush-rats (Mus rattus), which depend for food during a part of the year on the ripe berries falling from the trees, were likewise compelled to migrate in search of food. In the same year the habits of the kaka (Nestor meridionalis) and the silver-eye (Zosterops lateralis) were affected in a similar manner and from the same cause. I collected several specimens of the former in a plantation of English trees near Oamaru, all in a wretchedly weak and lean condition. Their presence was a rare occurrence in the district, which is about thirty-five miles from the nearest native bush. The silver-eye or “blight bird” frequented the gardens in the settled districts in unusual numbers, and attacked the ripe fruits, nothing coming amiss to them. All the species affected were in wretched plumage, and their bodies were infested with a species of Acarus.

The New Zealand quail (Coturnias novæ-zealandiæ) is often cited as showing how rapidly a species will become extinct. Frequently we hear the old colonists speaking of the great numbers of quail inhabiting the grassy plains in the early days of Canterbury. In a few years, however, without any apparent cause, they vanished, until at the present time not a single living quail exists in the islands. Their disappearance is generally attributed by ornithologists to the burning of sheep-runs or native-grass lands. Probably this is the principal cause which has effected the extirpation of this useful and beautiful gallinaceous bird.

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In the early days of the colony, when the species flourished on the plains, vast swarms of caterpillars infested the open grassy country, living in the dense tussock (Poa). In a few years after the annual burning of the sheep-runs commenced, the caterpillars disappeared from the plains and attacked the cereal crops, working great destruction among them. Some years after the introduction of the house-sparrow, which increased at an unprecedented rate, the caterpillars were soon reduced in numbers, and are now no more trouble to the agriculturist. They were the larva of the yellow underwing moth, still to be obtained feeding on the introduced Cape broom.

The moth (Botys polygonalis) is double-brooded, the first brood appearing in August and September, the second in January and February. The larva is abundant every year, often to such an extent as to cause the complete defoliation of the food-plant. The species would unquestionably increase, and probably again become troublesome to farmers, but for the presence of the house-sparrow, which hunts vigorously in the hedges for the larvæ, and keeps them in check. As the plant is not indigenous, the moth has apparently acquired a special taste in selecting it as the food of the larva, the colours of both assimilate closely, which affords some protection to the species.

On good land, where the tussock-grass is thick and allowed to remain unburned for a number of years, the ground is soon covered with a considerable thickness of dead grass. In this, many species of Coleoptera and the chrysalis of moths can, at all seasons, be found. Such were precisely the natural conditions of the plains in the days of the quail, excepting that they were on a superior scale, and the food-supply at all times more abundant. A fire sweeping over a large area of such country* would effectually annihilate all insect life in its course, and leave the country black and bare. Frequently the fires raged for several days and nights

[Footnote] * Some authors, writing on the moa age, maintain that fires were kindled for the purpose of driving the huge birds on to the sea-shore to enable the hunters to capture them more easily. Supposing such a theory to be tenable, it may be asked, “Why did not the quail become extinct with the moas?” In answer, it may be said that, if ever fire was used as an agent to destroy the moa, its ravages would be confined to small limits, and its progress intercepted by the rivers of the plains. I, however, am not a believer in the fire-theory put forth to account for the extinction of the Dinornis. To my mind, the thick grass would be a great protection to the hunters, and would be used by them as an ambush when tracking or surrounding the moas. If the quail existed in New Zealand along with the moas, the burning of portions of the grassy plains occasionally would scarcely affect the economy of the species. It is the annual and wholesale burning of the lands, and the clearing and cultivation that followed, which completed the work of extermination.

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together, and spread for many miles across the then open country.

Apart from the utter destruction of the food, the dense tussock afforded the natural warmth and shelter for the birds during inclement weather and chiefly inclement nights; the sudden removal of both would, therefore, act powerfully on the economy and habits of the quail. The species, like other birds in their respective orders now becoming extinct in New Zealand, was a highly specialised form among gallinaceous birds, and depended on special conditions, such as I have pointed out, for its existence. The effects of the fires and of clearing and cultivation on the climate, though perhaps at the time inappreciable to man, would aid likewise in exterminating the species.

No more interesting or profitable district could be visited by the botanist or ornithologist in New Zealand than around the shores of Lake Brunner. The magnificent primeval forest is due to the greater humidity of the lake valley as compared with many other parts of the west coast, and to the great depth of vegetable mould, or rich virgin soil, which covered the whole face of the country before the forest spread over it. I have seen most of the great bush-lands of New Zealand, but nowhere can the vegetation of the bush be seen in such profusion and perfection, rivalling in luxuriance the tropical American forests so fully recorded in the admirable works of Bates on the Amazons, and Belt on Nicaragua.

Among the rich groves of tree-ferns the kakapo (Stringops) and the kiwi (Apteryx) have their home. In the saplings of taller growth and among the branches of the towering timbertrees many birds revel and enliven the bush through the day with their rich and varied notes. As evening comes on, the calls of nocturnal and semi-nocturnal species are heard. In the dwarf ferns, the weka moves stealthily about, silently peering into the tent, ready to pick up any bright object and carry it off, to be left and lost in the bush. In the branches of decaying trees the kaka is busy searching in the bark and hollows for insects, uttering, as it flies from tree to tree, a hoarse discordant scream. The little owl (Spiloglaux) answers from all directions the call of “morepork.” The croaking of the kakapo, busily, among the ferns and lower branches, consuming the leaves, and the shrill night-cry of the kiwi, are the only sounds which nightly disturb the serene silence of the forest.

In my paper to-night it will be impossible to treat the subject so fully as I would wish in the limited time; I will, therefore, confine myself to a few remarks on each species in the list here appended. It is possible, however, that other species omitted from the list may exist in the lake region

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If so, they must be of rarer occurrence than any I have enumerated, and were never observed there by me. I may add that my object in writing this paper is to illustrate the ornithology of Lake Brunner as it is in 1888, and before the physical features of the country are changed and many of the birds become extinct in the district—a result which will inevitably follow the construction of the Midland Railway and the subsequent clearing and settlement.

Appended is the list of birds inhabiting the lake district.

Hieracidea brunnea (Bush-hawk).

It is intensely interesting to watch a pair of these falcons hovering and circling high above the bush, poising motionless for some seconds, and darting forward at intervals to perform their graceful circling flight, meanwhile uttering their “loud petulant scream.” Sir Walter Buller, in his great work on the birds of New Zealand, has described the vehement screaming of this hawk when flying high as an excellent indication of changes in the barometer. As there is more bad weather on the west coast than on the east, and the bird is common, I had good opportunities in the vicinity of the lake of noting the screaming of the bush-hawk in relation to the weather, and invariably found it to be succeeded by bad weather. The days on which they perform their high screaming flights is followed by nights of continuous and loud calling of the wekas and kiwis, both of which are equally good indicators of bad weather approaching.

The nest of this little falcon is placed on the top of some old dead tree-stem, broken off some distance from the ground, or in a hanging mass of climbers. It boldly assails any intruder near its eyrie, and screams vociferously while assailing him. As the food-supply is abundant around the lake, and the birds are rarely molested, they will remain common for some years to come.

Circus gouldi (New Zealand Harrier).

I observed the harrier occasionally circling around the mouth of the Ahuna River, an influent near the top of the lake, but it rarely enters the bush in search of prey. Judging from the direct line of flight I have observed them taking, I am of opinion that they pass up the Arnold River from the coast, and cross the open lake as a near route to the open country at the head waters of the Teremakau River, where the species is common. Owing to the dense bush it cannot procure food in the lake valley.

Spiloglaux novæ-zealandiæ (Morepork Owl).

Common around the lake and the whole course of the Arnold River.

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Stringops habroptilus (Owl Parrot, or Kakapo).

This remarkable bird is now becoming rare at Lake Brunner. It was exceedingly plentiful at the time of the Kangaroo gold-rush in the district over twenty years ago. Since then it has diminished in numbers, and bids fair to be numbered with other species now rapidly becoming extinct. Being nocturnal in their habits, they emerge from their hiding-places in the evening to feed, and climb among the lower branches, consuming the soft vegetation. When several are feeding together, they continue throughout the night to answer each other's calls, or hoarse mutterings, uttered while masticating their food. On very dark nights it is pleasing to steal as near them as possible and listen to them nibbling at the tender leaves, while they croak and mutter continuously. By the morning their crops are enlarged to their full extent with the nutritious green food consumed during the night. On moonlight nights their sight is clearer, and they take advantage of this to roam farther from their hiding-places to feed. On the outskirts of the bush several may be seen together waddling leisurely along towards some favourite feeding-grounds, returning, when their hunger is appeased, to their usual hiding-place. The latter is generally in or about the decayed roots of old trees or hollow prostrate trunks. It is sometimes easy to find their homes by the presence of little trodden paths leading to them.

Nestor meridionalis (Kaka Parrot).

The kaka parrot is very common in the lake valley. Belonging to the family of honey-sucking parrots, they repair in the spring to the blooming kowhai trees, and regale themselves on the flowers. While thus engaged, they allow a near approach. It is then most interesting to observe them climbing among the pale-green foliage and seizing a bunch of the yellow flowers, carefully and gently pressing the receptacle of the flowers between the tongue and softly-lined overlapping upper beak, and sucking the honey. The structure of the flower is peculiarly adapted to the process, which is performed without any injury to it. The kaka's repast is not, however, obtained without some effort. Naturally somewhat clumsy in their movements, they sometimes experience difficulties in reaching the masses of flowers on the tips of the branches owing to the very brittle nature of the twigs. They, however, fully realise this, and instinctively select the flowers on the stronger branches. When within reach, they hold firmly to the branch and, stretching the neck to its full length, seize and draw the flowers towards them with the beak. One foot is then used to hold the flowers, while the other holds firmly to the branch and steadies the bird when sucking the honey. The weight

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of the bird will sometimes cause the branch to bend down to the lower ones, which affords a slight support.

The kaka's habit of breaking twigs with its powerful beak when searching for food is simply to clear its course and to allow more scope and freedom to its movements.

Nestor notabilis (Kea, or Mountain Parrot).

Although the kea is not, as far as I know, an inhabitant of the naked mountain-tops overlooking Lake Brunner, I may here mention that the range of the species continues to extend farther north every year, and may soon extend to the higher ranges in Westland. When Sir Walter Buller published his last paper on the kea five years ago, he gave the ranges on the upper reaches of the Rakaia as its extreme northern limit. During the last three winters it has visited the ranges above the Otira Gorge, thus showing its range to be extending northwards.

Platycercus novæ-zealandiæ (Red-fronted Parrakeet).

P. auriceps (Yellow-fronted Parrakeet).

Both species are abundant in the bush around the lake, the first-named being the most numerous. In fruitful seasons the food-supply of the parrakeets in this district must be prodigious, the berry-bearing trees being both robust and plentiful. The two great irruptions during the last ten years must have considerably lessened their numbers. Severe, late, or early frosts are probably the chief cause of the failure of their food-supply, compelling them to cross over the ranges and devastate the orchards in the eastern districts. During the two irruptions they perished in thousands, as every possible method was tried to trap and destroy them; yet they compensated the settlers to a great extent by consuming the seeds of many noxious weeds, which they attacked when the green fruit in the orchards had been destroyed by them. I often observed them in large flights, consuming the seeds of Chenopodium urbicum, an introduced weed, which grows to the height of 4ft. and 5ft., and spreads rapidly. They vigorously attacked the seeds of the various species of Sonchus, or sow-thistles; the dock (Rumex obtusifolius), which grows in large masses on the bottom of sluggish watercourses; the Yorkshire fog (Holcus mollis); and many other injurious plants.

The present year has been an unprecedentedly cold and wet one on the west coast, the result of which will be worth noting, as bearing on the economy of the parrakeets and other species.

Eudynamis taitensis (Long-tailed Cuckoo).

Chrysococcyx lucidus (Shining Cuckoo).

Both species of migratory cuckoos; they visit the bush in

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the Grey Valley and Lake District annually in great numbers. They arrive in the first week in October and depart in the middle of March, the large Polynesian species being the first to depart, followed in a week or ten days by the smaller Australian form. After their arrival the long-tailed cuckoo is an object of almost continual persecution by the tuis, which boldly assail and pursue it through the bush, at the same time uttering their wild alarm-call. The superior and dashing flight of the cuckoo, however, soon places it out of danger for a time, and is its only mode of escape, as it is able to offer only a feeble resistance against a number of angry tuis.

Prosthemadera novæ-zealandiæ (Tui, or Parson-bird).

Anthournis melanura (Korimako, or Bell-bird).

In fine weather the bush along the south shores of Lake Brunner re-echoes with the rich notes of the tui and korimako, busy in their season among the blooms of the kowhai (Sophora tetraptera) and rata (Metrosideros robusta). There is no picture more beautiful in nature than the sight of these two charming songsters, clinging and swinging in grotesque postures in the sunshine on the brilliant crimson blooms of the rata, sipping the nectar, and flying every few minutes to some bough, and uttering their rich song. When suspended, the deep metallic lustre of the tui's plumage contrasts beautifully with the masses of crimson flowers during the season of rata blooms (March and April) so plentiful at the lake. The tui and korimako come to the trees and remain there so long as the blooms support them. They then disperse among the warmer valleys of the bush, and subsist during the wet winter months chiefly on insects, until the return of spring, when the melliferous blooms of the kowhai again supply them with the necessary food. Although both species have disappeared from, or have become rare in, many former haunts east of the Alps, they still exist in great numbers in the Grey Valley and throughout the Westland bush. The tui is much more numerous than the korimako.

Zosterops lateralis (Silver-eye).

This species is exceedingly common in the bush. As the colder weather sets in they congregate in flocks of several hundreds, and leave the higher bush-lands for the lower valleys, visiting the huts and villages of the diggers, voraciously devouring all suitable food which they meet with in their course. Like the kea (Nestor notabilis) they have acquired a stong penchant for fresh meat, especially raw fat. They eagerly attack the meat in the butchers' shops, fluttering over and hustling each other in their eagerness to obtain food. While thus engaged they utter shrill excited notes, which are pleasing to hear.

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Orthonyx ochrocephala (Yellow-head).

Commonest on the south shores of the lake. In some seasons it is more numerous thán in others. Some notes are given on this species, associated with the saddleback.

Gerygone flaviventris (Grey Warbler).

The grey warbler is plentiful in all the forests in Westland. As the chief foster-parent of the two species of parasitic cuckoos, the latter will never, under ordinary circumstances, become rare while the rearing of their young is intrusted to the care of this cheerful and industrious little bird. The warbler's merry song is heard throughout the day, as it actively flits through the undergrowth in search of food. It is exceedingly lively in all its actions. While warbling, the white-tipped tail is often spread to form a fan, and its whole motions are full of life and activity. The beautiful pensile nest it constructs is an interesting object in bird-architecture, the site selected being generally on the outer branches of the manuka (Leptospermum scoparium) or other dense small-leaved tree or shrub, where it is safe from the attacks of enemies. Although the grey warbler does not decrease in numbers, it cannot be classed with many otherwise favoured species, owing to its having a “double debt to pay”—namely, the rearing of its own brood and the young of the parasitic cuckoos; but nature has fully compensated for this by endowing the species with a life the most active, cheerful, and diligent of all our native birds, and thus enabling it to perform the onerous duties perfectly.

Acanthisitta chloris (Rifleman).

The feeble note of this diminutive bird is oftener heard in the bush than the bird is seen. It is more common near the summits of the lower bush-covered mountains near the lake than in the valleys. It is a very timid species, and has a habit of keeping on the opposite side of the tree-trunks to that on which the observer is moving, which explains the cause of it being very seldom seen.

Xenicus longipes (Bush Wren).

Common some distance up the bushy slopes, where the vegetation is not so dense as near the lake. It delights to climb the moss-covered saplings, searching for minute insects secreted among the moss. When disturbed it utters alarm-notes, which are answered by others near; at the same time it endeavours to conceal itself in the thickest scrub, or, hopping and climbing up the trees, it disappears among the higher branches.

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Miro albifrons (South Island Robin).

The wood-robin is an almost constant attendant when roaming in the bush or about the tents. Its habits are in some respects similar to the yellow-breasted tit (Myiomoira macrocephala)—jealously chasing each other round the tents, and disputing their rights to crumbs of bread or other food thrown to them. When seated outside the tent they will frequently settle on the boots, darting off to pick up crumbs, returning again and again, and becoming very familiar. They are encouraged and protected by the gold-diggers, who allow them to enter their tents and huts and to hop on the table to share their own meals. The song of the wood-robin in the lonely bush is in all seasons enjoyable. It is the first astir with the earliest streak of dawn, and, with the fantails, is the last to retire in the evening, when the gloomy twilight silently closes over the bush.

Halcyon vagans (Kingfisher).

The kingfisher is abundant about the lake, frequenting the mouths of the streams flowing slowly into it. The food-supply is enormous, as the shallow edges of the streams teem with the small bull-trout.

In autumn, when the grayling ascends the Arnold River, large numbers of kingfishers withdraw from the lake and subsist on the smaller-sized fish of this beautiful and useful species. When the colder months set in many descend the Arnold to the more open and sunny flats on the Grey River, subsisting on insects and small bull-trout “or bullys” until the arrival of the whitebait.

In the Grey during the whitebait season (September and October) the birds are very numerous, and can be seen sunning themselves on dead trees or old naked stumps all along the lower Grey Valley.

Myiomoira macrocephala (Yellow-breasted Tit).

Among the undergrowth of the bush the sprightly yellow-breasted tits flit gracefully about, and sportingly chase each other through the branches, gently fluttering their wings, erecting their crests, and uttering a suppressed twitter as they sit eyeing each other on the boughs or clinging to the stems of the trees, and exhibiting the peculiar jealousy of the wood-robin about the tents. They are plentiful in the district, and more wary than many other species. In the bush near old settled districts on the west coast they are still abundant. Their food, which consists of worms, larvæ, chrysalides, and insects, is plentiful in all seasons in the bush.

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Rhipidura flabellifera (Pied Fantail).

R. fuliginosa (Black Fantail).

On the outskirts of the bush the pied and black fantails are daily on the wing, eagerly consuming the sandflies so troublesome in the bush. In dull or wet weather these birds are busy on the shores of the lake, flitting lightly over the water beneath the overhanging branches, and performing graceful evolutions in the air in pursuit of their prey. Both species are abundant around the lake. Their food, the common sandfly (Limulia australiensis), is abundant—a fact which is well known to visitors or dwellers in the West Coast bush.

Turnagra crassirostris (South Island Thrush).

The South Island or thick-billed thrush is still fairly numerous at the lake, but has disappeared from the lower gullies of the Arnold, between Stillwater (now named Richardson) and the Arnold gold-diggings. Fifteen or twenty years ago this species existed in great numbers on the Maori Gully goldfield, and fed around the huts and tents of the diggers, frequently entering and hopping on the floors picking crumbs, but gradually their numbers diminished until at the present time not a single thrush exists on the goldfield. Like the British species (Turdus musicus), the early morning or evening is the best time to hear its splendid notes and call, or to study its habits, it being then most active. A few hours after sunrise they cease to sing or to answer each other's notes, and generally remain silent in fine weather during the day among the tree-ferns and lower branches of the trees. In dull or wet weather they move about among the higher branches in search of food, and avoid the heavy drip of the thick undergrowth. Like other species, as the wood-robin, the yellow-breasted tit, the crow, and weka, it is easily attracted to the spot where any unusual noise is produced in the bush near its haunts, often coming almost within reach of the individual attracting it, spreading its beautiful rich brown tail, moving sideways along the branch, and turning its body right and left, meanwhile examining the stranger closely. It is, however, a powerful flier, and flies with great precision through the tangled vegetation. I have observed it several times performing such flights; resting almost motionless for some minutes on a high limb of a tree, it would suddenly ruffle its feathers, and, dropping from the limb, fly with great force through the thick undergrowth, reappearing again on a high limb some distance away. One bird I watched uttered a wild jubilant note as it dropped from its perch to repeat its flights from tree to tree. It is probably a habit peculiar to the

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pairing season, as I never observed them performing such flights at other times of the year.

Glaucopis cinerea (Yellow-wattled Crow).

This is another remarkable and beautiful species now rapidly approaching extinction. Like other ground-feeders it is exceedingly tame, and falls an easy prey to dogs and cats, large numbers perishing annually from this cause alone. The nest, which is generally placed in some low scrub, is easily reached by cats and rats, and in some localities where both are numerous the parent birds rarely succeed in rearing a brood. While staying at Lake Brunner for fourteen months, and travelling great distances in all directions every day, excepting in wet or windy weather, we never obtained or observed a single young crow. Occasionally an adult bird came around the tents, moving spiritedly, and hopping tamely about the tent-door, picking crumbs or other suitable morsels of food, but only once did we observe a pair together. This occurred two miles up the Ahuna River from the lake, being at the end of October. They were probably paired for the season, and both were in perfect condition, the orange-coloured wattles being most conspicuous. One bird was slightly longer than the other, which, no doubt, was the male. We watched them silently for over an hour to ascertain if they were nesting. They, however, moved on through the bush towards the lake, when we left them, and returned on our course up the river.

Like the preceding species, the South Island crow is a beautiful object in its native haunts, its exceeding tameness allowing a close and perfect study of its habits. When observed clinging to the pale lichen-covered trunk of some old tree, or swinging on the large fronds of tree-ferns, it supplies a picture of bird-life only to be realised by studying birds in their native haunts.

An intelligent workman employed in the Land Survey Department informs me that the species is still plentiful in some of the south-west sounds.

Carpophaga novæ-zealandiæ (Wood-pigeon).

The wood-pigeon is exceedingly common in the Lake District. In fine weather large flights change quarters daily, flying from shore to shore or from one part of the bush to another to visit some favourite or seasonable berry-bearing trees. The presence of numbers of this splendid pigeon in March and April among the graceful foliage of the miro trees (Podocarpus ferruginea), moving through the branches and plucking the large fleshy scarlet berries, is another charming picture of bird-life in the New Zealand bush. A plentiful season of miro berries is invariably followed by a season of fat

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pigeons. The berries are much relished by the birds, and are exceptionally nutritious and fattening. The nest of this species is placed in the thickest branches of the white and silver pines. As little wind blows in the spring in the forests of the west coast, they experience few difficulties in rearing a good brood annually.

The plumage of the wood-pigeon high among the branches is striking, the bronze-burnished pectus and white abdomen contrast beautifully with the green forest around.

Creadion carunculatus (Saddleback).

This species is sometimes gregarious, and moves through the bush during the colder months of the year in flights of from a dozen to fifty or more together. Several of the old gold-diggers on the River Arnold informed me that they have frequently observed flights of the saddleback following the flights of canaries (Orthonyx ochrocephala) as they fed through the bush. Probably no scene in bird-life is more attractive or beautiful than to observe a flock of yellowheads followed by a flock of saddlebacks. On the 2nd June, 1887, I rambled up Stoney Creek, a small stream which flows into the lake a little above the outlet of the Arnold. I had travelled on the banks and bed of the creek about a mile when I turned to the right, up a small narrow gully, in search of ferns or other botanical rarities. On reaching nearly the top of the gully, I heard the shrill, ringing notes of a flock of yellowheads. As I noticed them crossing the gully some distance above me, I moved on gently until I was under the branches on which the birds were passing over the gully. They numbered about two hundred, and were in rich plumage. They fed eagerly for some minutes among the branches of the trees; then, simultaneously uttering their call, they flew forward some yards and began to feed, until they again sounded the signal to advance, repeating it at short intervals, and passed on through the bush in this order.

Before the yellowheads had quite disappeared I heard the rich flute-notes of a flock of saddlebacks advancing. I climbed up the side of the gully and stood on the edge. Two males were the first to appear, followed by the remainder of the flock. They advanced in the line of the yellowheads; not so high among the branches as the latter, but more among the tree-ferns, while some fed among the ferns and mosses covering the ground. When they noticed me some approached closely, twittering, and elevating their tails. They moved about in a sprightly manner on the lower branches, within a few feet of my face, scanning me carefully, and wondering, perhaps, at the intruder on their solitary domain. They were exceedingly tame, and moved with great activity, halting at

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intervals, and resting their breasts for a few seconds on the boughs, and again proceeded, searching eagerly for food among the ferns and mosses covering the ground. They were in the perfection of plumage. The saddle-shaped patch of rich brown extending over the back and shoulders, on the lustrous black ground, contrasted well with the deep green fronds of the tree-ferns. The sexes were about equal, and the plumage of some paler than others, which were young birds. They remained hopping on the branches and ferns near me for about seven minutes, and disappeared slowly in the track of the yellowheads.

The purpose served in the saddlebacks' economy in following the flocks of yellowheads is unquestionably to obtain food. The latter, in moving through the bush, will disturb numerous large insects, which they reject, and which are consumed by the saddlebacks following them. The rich insect fauna in some parts of the bush in Westland at certain seasons will account for the appearance of flocks of the native insectivorous birds in these districts. The flights of yellowheads must be entirely regulated by, or restricted to, the supply of food. Where the bush remains in its primeval state they remain numerous; where it is partly cleared or disturbed, this species and many others diminish in numbers and ultimately vanish from the locality. Although the saddlebacks are not dependent on the flights of yellowheads for food, they are able to obtain such by following them, and do not always travel in flocks, as they are occasionally seen singly and in pairs, in some of the gullies of the Arnold and around the lakes, but are now very rare compared to the numbers which inhabited the banks of the Arnold fifteen or twenty years ago.

I was attracted early one morning in March towards some old fallen and decayed timber, where I heard some peculiar tapping sounds. On cautiously reaching the place I found a saddleback busily digging in the decayed timber for the larvæ of the huhu beetle (Prionoplus reticularis). The tappings and actions of the bird resembled much those of the green woodpecker (Picea viridis) of Britain in its mode of procuring food.

Ocydromus australis (South Island Weka).

Common on the bushy slopes of the mountains on the north side of the lake. It is more common in the valley of the Crooked River than near the shores. They are exceedingly tame and inquisitive, and come about the tents, often remaining around the camp for weeks, picking up crumbs of bread or scraps of meat thrown out. When a number collect near the camp it is almost impossible to sleep, owing to their loud calls through the night. They give much trouble

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in camp by entering the tents and pulling or tossing over all movable objects, unless all is left secure.

Ocydromus fuscus (Black Weka).

This darker species or variety is not so plentiful as the preceding one. It inhabits the slopes of the lower bush-clad mountains bounding the lake on the south. It is also a more timid form. But there is no appreciable difference in their call, excepting that this species is slightly the shriller of the two.

Ortygometra tabuensis (Swamp-crake).

The swamp-crake is uncommon about the lake. It frequents the shallow lagoons, concealing itself in patches of Carex growing around them.

Porphyrio melanotus (Swamp-hen).

Common in the more open places. They appear to obtain good food, as all I observed were exceptionally fine birds, in perfect plumage.

Himantopus leucocephala (White-headed Stilt).

H. novæ-zealandiæ (Black Stilt).

Both species frequent the shores of the lake and the narrow sandy flats on the Ahuna and Crooked Rivers, the former being the most numerous. It is interesting to stand among the thick vegetation, or behind some tree, and watch them stalking gracefully along the shallow shores in search of food, suddenly taking flight and flying some distance, to recommence the search in fresh places.

Strepsilas interpres (Turnstone).

Occurs among the rough beds of boulders on the Ahuna River, but never at any time numerous.

Hæmatopus longirostris (Pied Oyster-catcher).

H. unicolor (Black Oyster-catcher).

I observed three specimens only of the first-named species at the lake, but I occasionally heard them flying over the district seawards at a great height. The black species inhabits the sands near the mouth of the Ahuna River, but is never very plentiful.

Ardea alba (White Heron).

This magnificent bird—the white, crane of the Europeans, the kotuku of the Maoris—still lingers among the secluded lagoons on the bush-flats in the vicinity of Lake Brunner. They are beautiful objects when seen sitting leisurely on the edge of the water. When alarmed they rise, flapping somewhat clumsily, ascending spirally in the air until a considerable height is reached; then, taking some more direct course, the legs are drawn up close to the tail, and they sail away

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lightly through the air. I regret that time will not allow of my adding a few more remarks on this splendid species.

Ardea sacra (Blue Heron).

Common in the summer and autumn, when eels and grayling are plentiful in the Arnold and the lake.

Ardea maculata (Little Bittern).

I lately sent a note to the Ibis announcing the capture of two specimens of the little bittern on the west coast within the last four years. One was taken at Lake Brunner four years ago; the other was shot last year in a lagoon north of Okarita, and is now in a private collection at Ross. In a rough country like the west coast, still imperfectly explored by ornithologists, it is probable the species may exist in good numbers among the remote lagoons. Naturally an exceedingly shy form, it would readily escape notice, as it is difficult for dogs to work or flush game out of the thick grass and sedges which generally cover the water in a dense mass. I have no doubt that other specimens will be collected as the country becomes cleared.

Botaurus pæciloptilus (Bittern).

Not uncommon among lagoons formed by small arms of the lake, or in the small bays choked with weeds. Also a shy species.

Anas superciliosa (Grey Duck).

During the shooting-season they appear in immense flocks on the lake. They are probably driven thither or take refuge on its waters from the guns of sportsmen in the Grey Valley and other localities. The food-supply is abundant in the weedy creeks and bays of the lake. All the birds we procured were in good condition.

Hymenolæmus malacorhynchus (Blue Duck).

More common on the Arnold River below the lake than elsewhere, where they rest on the stones jutting out of the rapid stream. They ascend the creeks in the bush where they find an ample supply of food. When wounded they are expert divers, diving in the rapid waters and reappearing long distances down stream.

Querquedula gibberifrons (Little Teal).

Common in some parts of the lake, about the sluggish creeks entering it.

Fuligula novæ-zealandiæ (New Zealand Scaup).

Not uncommon in the smaller bays, where it takes refuge among the beds of Carex and raupo.

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Casarca variegata (Sheldrake or Paradise Duck).

This beautiful species is the largest and handsomest form in the order Anseres in New Zealand. It delights to live in the open country near broad river-beds composed of shingle and sand, or on grassy flats near lakes or pools of clear water. It is generally met with in pairs, but can often be seen flying in flocks, changing quarters from one district to another. Occasionally they reach Lake Brunner and disperse along the shores to feed for several days. Reassembling in a flock, they again take flight and leave the lake. Some years they are common in the valleys of the Grey and Teremakau Rivers, frequenting the sandy flats. Owing to the periodical flooding of these two great rivers they are compelled to seek fresh feeding-grounds, and during these short migrations they visit the lake.

C. variegata (Shoveller Duck).

The shoveller or spoonbill duck frequents the larger bays on the west side of the lake. I have detected them among the flocks of grey ducks resting in clear weather on the open lake, but never numerous. They are beautiful objects on the water in spring followed by a brood, and allow a near approach, gliding gently along the shore or into some sluggish creek to nibble among the weeds, or macerating vegetation to procure food for their young. On the west coast their food must differ considerably from that on the east, where they generally inhabit the estuaries of rivers.

Larus dominicanus (Southern Black-backed Gull).

L. scopulinus (Mackerel Gull).

The former is very common during the summer; the latter is an occasional visitant at the lake.

Sterna antarctica (Grey Tern).

Common in the nesting-season in the lake valley.

Podiceps cristatus (Crested Grebe).

The crested grebe has here a safe retreat from the ravages of sportsmen or collectors. No eye can equal the grebe's in its quickness of vision, nor can any bird compare with it for rapid diving. When feeding unobserved along the shore they are gentle and graceful, yet wary, in their movements. When alarmed they draw off into the open lake and are soon lost in the expanse of water.

Podiceps rufipectus (Dabchick).

Not uncommon on the lake; likewise expert divers. They frequent the bays on the north-west shore more than elsewhere, and are generally met with in pairs.

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Phalacrocorax novæ-zealandiæ (Black Shag).

P. varius (Pied Shag).

P. brevirostris (White-throated Shag).

All these species inhabit Lake Brunner and the rivers of the lake valley, the pied and white-throated species being most plentiful. There is an ample supply of food at all seasons in the form of eels, grayling, and the two species of bull-trout. There are two shaggeries of varius on the Arnold, one on each side of the river below the lake, having about sixty nests in each, placed on trees all more or less overhanging the river. In fine weather they delight to rest in groups of young and old together on gnarled leaning stumps along the shore, some leisurely picking and oiling their feathers, others in easy natural positions, with the head under the wing or drawn close into the body, the plumage of the white-throated shag reflecting brilliantly in the sunshine. Like the blue duck, they rest frequently on the projecting boulders in mid stream, enjoying the spray of the surging waters.

Apteryx australis (South Island Kiwi).

The South Island kiwi exists in considerable numbers in the bush around the lake. It is most numerous on the east and north-east sides, where large patches of Sphagnum moss (S. cymbifolium) cover the damp bottom of the bush, in the places where the trees and undergrowth are thinnest. They generally live in pairs, and during the night visit the beds of Sphagnum moss, probing carefully through it with their long sensitive bill in search of minute larvæ, chrysalides, and worms. They affect the beds of leaf-mould, and probe vigorously through it procuring the large worms existing in the mould. They ramble through the night among the dense beds of ferns, consuming nocturnal insects. Their shrill call is heard loudest on dark and drizzly nights, or before rain, and is answered by other kiwis in every direction.

After examining some of the secluded habitats of the rarer species of birds on the west coast, I have no doubt that an ornithological ramble through the Westland bush, accompanied with one or two good dogs, would yet reveal the existence of Notornis mantelli, as the species is of shy and retiring habits. It would in all probability be found in the swampy parts of the bush, or about the sedgy lagoons some distance inland on the southern rivers of Westland. The country is difficult to explore, being composed for the most part of dense and trackless forest. The capture of a single specimen of this rara avis would, however, amply repay for all patience and toil expended in exploring the bush. If the Notornis still lingers in the South Island, the district I have mentioned is

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one of the most favourable where a search may be made for this much prized bird.

The roaroa, or great kiwi (Apteryx haasti), is captured occasionally by survey-parties in southern Westland; and this, along with other valuable species, would probably reward the ornithologist for a trip through the west coast bush.

Art. XXII.—On Apteryx bulleri.

[Read before the Wellington Philosophical Society, 13th June, 1888.]

During a recent examination of some skins of Apteryges, in company with Sir Walter Buller, I became firmly convinced that the ordinary brown Apteryx of the North Island is certainly specifically distinct from the Apteryx australis of the South Island; and I was a little surprised to find, on going over the literature of the subject, that, notwithstanding a similar verdict on the part of such excellent naturalists as Sir James Hector, Sir Julius von Haast, Professor Hutton, Mr. Potts, and others, the North Island bird has not yet received a distinctive name. It has generally been called by naturalists Apteryx mantelli of Bartlett, under which name it appeared in the first edition of Buller's “Birds of New Zealand;” and it is the Apteryx australis var. mantelli, of Finsch's paper in the “Journal für Ornithologie,” 1873, p. 263. The characters given by Mr. Bartlett for his Apteryx mantelli are founded on the natural variations in Apteryx australis, of which A. mantelli is a pure synonym; and the North Island Apteryx awaits a title. The pair of adult birds in Sir Walter Buller's collection are relatively much smaller than the corresponding sexes of A. australis, and the colour is of a blackish brown instead of a tawny tint; while the curious harsh structure of the plumage, especially of the feathers of the rump and nape, is a further character of importance.

It gives me great pleasure to adopt a suggestion of my friend Dr. Finsch that the North Island Apteryx should be called Apteryx bulleri, after the learned author of the “Birds of New Zealand,” a work which in its first edition seemed to me to be as complete as it was possible to make a history of the birds of any single area, until I saw the magnificent new edition on which Sir Walter Buller is now engaged, and on the completion of which I should think any one would find it difficult to write anything more about the birds of New Zealand.

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Art. XXIII.—Notes on the Decrease of Pheasants on the West Coast of the North Island.

[Read before the Wellington Philosophical Society, 17th October, 1888.]

That the pheasant has to a great extent disappeared from the more settled portions of the Wanganui district, where it was formerly plentiful, is an admitted fact; but the causes of that fact are a matter that may be well considered open for discussion. The primary cause is, I think, the great increase of the weka, and the predilection these birds have acquired for eggs. When the pheasants were first introduced into the district they soon increased, and in a few years large bags could be obtained. But at that time the natives lived at many small settlements interspersed, as it were, among the whites; these natives kept a large number of dogs, which were scantily fed, and which, being driven to forage for themselves, lived principally on the weka. The dogs disappeared with the Natives: and to this cause, and also to the large increase of furze hedges, may be attributed the abnormal number of wekas that may be seen any dusky evening in the country; for the furze hedges swarm with them. Now, it is well known that wekas are very fond of eggs, and during the last ten years it is the experience of many farmers' wives that they can get no eggs at all unless the fowls are kept shut up until they have laid; for all nests that were made even quite close to the homestead were and are speedily destroyed, the eggs being eaten by the weka. Wherever the natives are settled it is noticed that there are plenty of pheasants. The habit of keeping a lot of dogs and hardly feeding them at all, thus forcing the dogs to hunt for themselves, and there being generally less furze at native settlements, the wekas cannot so readily escape, and they are thus kept from unduly increasing. When the wekas first acquired a taste for eggs is a matter for conjecture. Is it in their case as with the kea's penchant for kidney-fat, and the Nelson parra-keet's proclivity for cherries? I am rather inclined to think it is, but I have no proof. Certainly hens' eggs were not destroyed twenty years ago as they are now, for fowls were allowed to run and breed anywhere. And here it might be asked, how do the wekas discriminate between the eggs of their own tribe and those of other birds? Is it because they cover them? or do they distinguish?

Then there are other reasons: hawks attack the young and sometimes the adult pheasant ; rats no doubt assist in eating the eggs; and in those districts where poisoned grain is used it goes without saying the pheasant soon disappears. And in

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addition to all these causes there is the fact that the settlers' sons, who were children when the pheasant was first plentiful, are now grown up, and where one gun was carried, now two or more are added; but I think the weka the principal cause. For, at the Maori clearing on the Wanganui River pheasants are plentiful, as also on the Waitotara River ; and they are also to be found, though not so numerous as at Maori settlements, in the newer bush-country opened up during the last four or five years in the Wangaehu Valley. But it may be noticed that as Maori dogs disappear and furze hedges increase the pheasant decreases, and it is very hard to suggest a remedy. The Acclimatization Society for years spent a considerable sum in buying wekas' heads, and thousands were paid for each year, but no perceptible decrease has been noticed, and at last the society have discontinued the practice.

Art. XXIV.—The Takahe (Notornis mantelli) in Western Otago.

[Read before the Wellington Philosophical Society, 17th October, 1888.]

Up to the present time only three specimens of this remarkable bird have been secured, and, as the opinion has been expressed by some naturalists that it is now quite extinct, I have prepared the following notes, collected during the progress of various explorations in Otago, as tending to show that it not only exists, but is probably as numerous now as when the colony was first settled by Europeans.

I may mention at the outset that the genus Notornis was founded by Professor Owen in the year 1848, upon portions of a skull and other parts of the skeleton of a large rail discovered at Waingongoro by the Hon. Walter Mantell, while exploring at that place for moa-bones. These fossils are all that now remain to testify the existence of the Notornis in the North Island, where it was known to the natives as the moho.

By a strange and, at the same time, most fitting coincidence, the first two specimens of the Notornis, or takahe as it was called in the South Island, were secured by Mr. Mantell in 1849. The first of these was captured by a party of sealers at Duck Cove, Resolution Island, in Dusky Sound ; and the second by the Maoris on Secretary Island, opposite to Deas Cove, in Thompson Sound. Both of these were forwarded to England, and are now in the British Museum in London.

After a lapse of over thirty years the third specimen was

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captured by a party of rabbiters about the beginning of 1880, on the Maruroa Flat, on the east side of Lake Te Anau. This bird was also sent to England, and at the present time probably adorns the shelf of some foreign museum. Since the above date no fresh example of the Notornis has been secured, although much time has been spent in the search around Lake Te Anau.

My first acquaintance with this bird dates back to 1881. During the months of January and February of that year I was engaged, with Mr. A. McKay and Mr. John Buchanan, on a geological and botanical exploration of the Wanaka country. On the 20th of January we struck our camp at the forks of the Matukituki, opposite Mount Aspiring, and proceeded up the south branch of that river to Cascade Creek, a distance of eight or ten miles. Here we pitched our tents, at an altitude of 2,000ft. above the sea, in the shelter of the Fagus bush which covers all the slopes of the surrounding mountains and the greater portion of the river-flats.

Shortly after dusk our attention was attracted by the call of a strange bird which approached within a few chains of our camp, uttering at short intervals a loud booming note. Now, we were all pretty familiar with the calls of the different birds usually met with in the high lands of Otago, but the call of this bird was quite unlike any of them. We knew also the booming note of the bittern, which, although like this in kind, was left far behind both in volume and intensity. Besides, this was a high, mountainous, bush-covered country, ill adapted for this bird, which usually frequents raupo-swamps and creek-banks. After some deliberation we arrived at the conclusion that this was the Notornis, a determination subsequently borne out by facts which came under my own observation.

The next evening, with Mr. McKay's assistance, I lit a large bright fire in the bush, about four chains from the camp, knowing from experience that birds of nocturnal habits were often attracted by the light of a camp-fire. Retiring a short distance from the fire, we awaited the result. As we anticipated, in less than half an hour our friend of the previous evening approached, uttering his booming note as he walked about. We now crawled towards the fire, making as little noise as possible in passing over the dry twigs and leaves lying upon the ground. When we drew near, the bird retreated from the opposite side of the fire, and when we withdrew it again approached. This manæuvre was repeated several times without any success on our part; but at the same time it should be mentioned that the bird, by its movements, exhibited no signs of haste or alarm.

On several occasions we were probably within four yards

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of it, and at these times when it uttered its note we could distinctly feel the ground vibrate beneath us. We, however, failed to catch a glimpse of it, as in the intense darkness of the forest this was quite impossible, excepting it chanced to get between us and the fire, which it carefully avoided doing.

The next day I examined the scene of the previous night's adventures, and found that the clear space below the matted branches of the scrub under which the bird had eluded us was about 20in. high, thus affording a means of approximately determining its height.

The Notornis remained in the vicinity of the camp during our stay at this place, being evidently more curious than alarmed at our presence. He generally sallied forth at dusk and retired at daybreak, his deep note completely dwarfing the cries of the kiwi and noisy kakapo.

On the 29th January we struck our tents and returned to our old camping-ground near the forks of the Matukituki. Shortly after dusk of this evening we heard the note of a Notornis, and, proceeding up the south branch to the upper end of the gorge, I disturbed the bird under a sandbank close to the river. On examining this spot I found that it had scraped a shallow hole in the dry sand, after the same manner, and probably for the same purpose, as the common barn-door fowl.

The river-flats at this place, situated about 1,700ft. above the sea, are covered with a scanty mixed bush, affording but little cover; the ground, however, is thickly strewn with large masses of rock which have fallen from the steep cliffs on the south side of the river, and below which the Notornis no doubt found shelter during the day-time.

The next evening I again proceeded to the upper end of the gorge, where the Notornis announced his arrival by his loud note. Knowing where to look for it, I approached the bank as cautiously as possible, but, just as I looked over, it scampered away as fast as it could run.

On this occasion I was fortunate enough to catch a passing view of it, although in the uncertain starlight I could only make out its general outline. It must be remembered that it was only in sight a few seconds; but the impression it left upon my mind at the time was that its colour was very dark, and its height about that of a full-grown turkey. An important fact to be noted here is that, although I got within a few feet of it, the bird made no attempt to fly, but ran away very swiftly, and without making any sound or cry of alarm. There can be little doubt that with a sharp dog I could easily have caught it ; but, unfortunately, we had no dog attached to our camp at this time.

Seven years now elapsed before the Notornis again came

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under my observation. At the beginning of this year I visited Dusky Sound for the purpose of examining the mineral deposits discovered there by Mr. William Docherty, the well-known prospector. On the day after my arrival—the 5th January—I accompanied Docherty to his pyrrhotine lode on the lower slopes of Mount Hodge, situated about a mile from the beach. Shortly after commencing the steep ascent we heard the deep booming call of a bird, which I at once recognised as similar to that of the strange bird I had heard in the Matukituki Valley in 1881. After listening for awhile I expressed my belief that this was the Notornis. Docherty, however, stoutly denied this, stating that he had often heard the same sound, which was what he called in his own words “a volcanic noise in the bowels of the earth.” Without stopping to argue the point, I pressed along, hoping to see the bird, which appeared to be somewhere on our path. The ascent at this point was very steep, our track being along the right bank of a precipitous rocky stream. In a few minutes we got so close to the bird that there could be no doubt whatever as to the organic origin, so to speak, of the sound, which seemed to proceed from the crop of the bird. I now told Docherty to keep quiet for a little, and he would soon see the cause of the booming, at which he became very excited, and shouted loudly that nothing would convince him it was not “a volcanic noise.” I need hardly state that we heard nothing more of this bird that day.

On returning to the hut in the evening my field-hand informed me that when he was fishing off the point close by he had heard a takahe in the bush in the direction in which I had been during the day. On asking him what he knew of that bird he said he was one of the party of rabbiters who caught the takahe near Lake Te Anau in 1880 ; and, as he had often heard the call of that bird and its mate, which, by the way, was never captured, he was quite sure the booming note which he had heard during the day was that of a takahe. In view of the determination I had previously arrived at, I considered this evidence conclusive that this was indeed the Notornis. I may mention that this was the first occasion on which I heard the Notornis spoken of as the takahe, the only name by which it was known to my field-hand.

That same evening, and every successive evening afterwards during my stay at Dusky Sound, I heard two takahes in the bush at no great distance from the hut. In the course of my various excursions in this sound I heard the takahe at the following places, not including those already mentioned : In the left-hand branch of Docherty's Creek, not far from the open country ; at the north end of Cooper's Island; in a gully on the southern slopes of Mount Pender, apparently not far

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from the beach ; and on the south side of the sound, about opposite the upper end of Cooper's Island.

It will be remembered that the first specimen of Notornis, secured by Mr. Mantell, was captured at Duck Cove, Resolution Island, a distance of some seven miles from Cooper's Island ; and the second at Secretary Island, in Thompson Sound, about thirty miles further up the coast. After a lapse of over thirty years a third specimen was captured in 1880, near Lake Te Anau; and the following year it was heard in the Upper Matukituki Valley, behind Mount Aspiring, by myself and others of an exploring party ; and now, again, in the beginning of the present year, at Dusky Sound, by myself and others. When passing through Wellington some four months ago Docherty informed the Hon. Mr. Mantell that he had recently seen a Notornis at Dusky Sound. He said he came upon it in the bush close to the beach, and that it flew some distance on to the water, and then made back to the shore.

I think I have said enough to show that the Notornis still exists in the lonely sounds and mountain-recesses of Western Otago, in places far removed from the ordinary haunts of men. That it is gradually becoming extinct is no doubt quite true, but, whatever the cause, it can hardly be said to be on account of the inroads of man. Its extinction is, possibly, partly due to scarcity of food, and partly to a process of natural decay which is no doubt in a measure induced by the effects of the first.

So recluse and retiring in its habits, it is probable that few if any further additions will be made to the three specimens of this bird already secured, unless special efforts be made in this direction; and, though this may entail a considerable expenditure of time and energy, the object is one deserving the support of every true naturalis.

Art. XXV.—Notes on some New Zealand Birds.

[Read before the Wellington Philosophical Society, 13th February, 1889.]

1. Rhipidura Fuliginosa (Black Fantail, Tiwakawaka).

This bird is generally believed to be confined to the South Island. There are, however, several well-authenticated records of its capture in the North. A specimen was quite recently shot at Levin, a new township on the Wellington and Manawatu Railway Company's land, and presented to the Colonial Museum by Mr. Charles Gillespie.

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I have been informed by a settler in the Manawatu district that the season before last a pair of them nested in the bush at the back of his property, and successfully reared their brood. He is positive as to the species. This would seem to show that they are not quite so scarce in the North Island as is usually supposed, even if they are not to be doomed indigenous.

2. Carpophaga novæ-zealandiæ (Wood-pigeon, Kuku, Kereru).

I have yet another instance of abnormal colouring of this magnificent bird to record. The specimen was shot at Kaikoura in June, 1887, and presented to the Colonial Museum by Mr. H. Inglis. The following is a description of it : Head, neck, and breast, normal colour, but of a duller shade. Hind-neck and front portion of scapulars and wing-covers rich brown, profusely interspersed with white (the body of each feather is quite white, but broadly tipped with rich chocolate-brown, which gives the colour to those parts); hind portions of scapulars, and wing-covers, white, the feathers in some places tinged and edged with slaty-grey; shafts of feathers deep-brown, almost black. Wings slaty-grey, much blotched with white, the feathers in most instances edged with coppery-green, shafts normal colour. Rump white, but bluish-grey feathers are profusely mixed. Tail-feathers white, but margined all round with bluish-black, shafts black ; below these feathers are white, but so thickly spotted with brown as to appear of that colour; the two outer shafts are nearly white. Abdomen and lower tail-cover white. Sides and lining of wings pale silvery-grey, in places almost white. Beak and feet normal colour.

3. Lobivanellus lobatus (Wattled Plover).

In a previous volume* I recorded the occurrence of the masked plover (L. personatus), in New Zealand. The identification was made from a drawing and description supplied to me, but I have since had an opportunity of examining the specimen, which Mr. Drew, in whose possession it is, kindly brought to Wellington for my inspection.

I find that the previous identification was incorrect—that the species is really L. lobata, the wattled plover; I therefore hasten to correct the mistake. The two species are very similar, the most striking difference being the amount of black on the neck, which was not sufficiently shown in the sketch.

This species is called the “alarm-bird” by the settlers in some parts of New South Wales, on account of its habit, when disturbed, of rising in the air, flying about excitedly, and

[Footnote] * “Trans. N.Z. Inst.,” vol. xx., p. 33.

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screaming so loudly that every creature within reach of its cry is on the alert.

4. Chætura caudacuta (Spine-tailed Swift, Needle-tailed Swallow).

Mr. Drew also brought with him a very good specimen of this bird. It was shot at Manaia, Hawera County, in March, 1888, and was given to the present owner by Mr. Budge. This latest visitor is a female, as proved by dissection, the only difference between the sexes being that the male is rather larger than his mate. This species has a wide range—it is said to breed under the snow-line in the Himalayas, it was found by Von Schrenck in Amoorland, it has been captured in England, is common in Australia, and now has visited New Zealand. Large flocks visit the eastern parts of Australia and Tasmania in the summer, but only stay a short time. It is probable that our specimen was merely an exhausted straggler from one of these flocks. It agrees well with the description given by Gould: “Crown of head, back of neck, and ear-coverts, deep shining-green, strongly tinged with brown; a small space immediately before the eye, deep velvety-black; band across the forehead, throat, inner webs of the secondaries nearest the back, a patch on the lower part of the flanks, and the under tail-coverts, white; wings and tail deep shining-green, with purple reflections; centre of the back greyish-brown, becoming darker towards the rump; chest and abdomen dark clove-brown.”

Mr. Gould makes the following remarks with regard to the enormous powers of flight possessed by this bird:—

“The keel or breastbone of this species is more than ordinarily deep, and the pectoral muscles more developed than in any bird of its weight with which I am acquainted. Its whole form is especially and beautifully adapted for extended flights; hence it readily passes from one part of the world to another, and, if so disposed, may be engaged in hawking for flies on the continent of Australia at one hour, and in the next be similarly employed in Tasmania.

“So exclusively is this bird a tenant of the air that I never in any instance saw it perch, and but rarely sufficiently near the earth to admit of a successful shot; it is only late in the evening, and during lowery weather that such an object can be accomplished. With the exception of the crane, it is certainly the most lofty as well as the most vigorous flier of the Australian birds. I have frequently observed in the middle of the hottest days, while lying prostrate on the ground, with my eyes directed upwards, the cloudless blue sky peopled at an immense elevation by hundreds of these birds, performing extensive curves and sweeping flights, doubtless

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attracted thither by the insects that soar aloft during serene weather.”

5. Phalacrocorax Punctatus (Spotted Shag).

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I have already published a description by Mr. McLean of the nesting of this species, as observed near Cape Kidnappers. He has since forwarded me an egg, taken from the nest by himself. It measures 28/20in. in length, by 18/20in. greatest diameter.

Art. XXVI.—The Mole-cricket (Gryllotalpa vulgaris) in New Zealand.

[Read before the Wellington Philosophical Society, 25th July, 1888.]

It is generally believed that New Zealand has no native mole-cricket: this belief is probably correct—at any rate, its existence has yet to be proved; though it is stated, on the authority of Mr. Churton and Major Parry, that one species (Gryllotalpa africana) has been found here. This species has, however, a wide range, being found in South Africa, India, and Australia. It is probable that the specimens referred to were introduced from the last-mentioned country; and Professor Hutton, who compiled the “Catalogue of New Zealand Orthoptera” published by the Colonial Museum and Geological Survey Department in 1881, states that he has never seen New Zealand specimens.

I have on previous occasions had to bring under the notice of the society the occurrence of European butterflies and of the scaly lizard in this country, and pointed out that as cultivation extended, and the importation of plants increased, so the introduction and spread of noxious insects would increase, and their depredations become more serious.

The most recent addition of this kind is the English mole-cricket. Some years ago a specimen was brought to me by a son of the late Rev. Mr. Harvey, and I was assured that it had been captured in New Zealand. I, however, took little notice of the matter at that time, and neither saw nor heard anything of further specimens till a short time ago, when I observed some children with the two specimens I now exhibit. The youngsters stated that they had dug them out of a bank on the Tinakori Road, near the Botanical Gardens. Both specimens are immature, but undoubtedly belong to the European species.

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In England and on the Continent—especially the latter—the mole-cricket is a terrible trouble, doing incalculable damage in the cornfields, pastures, and gardens. Germany and the south of France suffer most extensively, but the pest is gradually and surely working its way northwards, and is also common in many parts of England, especially in moist districts.

In Germany they have been known to destroy as much as one-fourth of the young corn-crop. They are also very fond of peas, beans, cabbage, and lettuce. Should they find their way into a kitchen-garden they will sometimes destroy whole beds of young plants in a single night. They burrow in the ground and eat the roots, so that the destruction is complete.

One species has of late years caused enormous damage amongst the pastures and sugar-cane plantations in the island of St. Vincent.

They live underground, are large and very powerful, and are said to be capable of propelling a 61b. weight on a smooth surface. Their fore feet are like those of a mole, and are peculiarly adapted for burrowing. During the day they remain in their burrows, along which they can move backwards or forwards with equal facility, being provided with two filaments at the end of the abdomen, which are used when a backward movement is desired.

These insects are probably familiar to some of you, and I have here specimens and drawings which may be examined, so that it is not necessary I should inflict on you a description of their personal appearance.

At the beginning of summer the female excavates, near her burrow, a cavity shaped somewhat like a lemonade-bottle, with a long neck, which is turned up and communicates with the surface and with her burrow. In this chamber she deposits some three or four hundred eggs. She then carefully seals up the entrance. In about a month or five weeks these eggs, which are about the size of small peas, hatch out, and the young at once commence to feed upon the tender roots of the surrounding plants.

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When first hatched they measure only from 1/12in. to ⅛in., and are destitute of wings, but when adult they measure nearly 2in., and have wings.

They pass the winter months in the earth, coming forth as spring advances. Their presence may be traced by the little mounds of earth like miniature molehills, and by the yellow withered patches which disfigure pastures and gardens.

I have now seen three specimens captured in New Zealand; it is therefore reasonable to suppose that they have, to some extent at least, established themselves here, and it is probable, in consequence of the rapid progress new pests

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always make in this country, that in time, unless great care is taken, we may find the mole-crickets as troublesome as they are in Europe.

Luckily, there are numerous ways of getting rid of them, and nature helps considerably, for the mother herself frequently eats large numbers of her children. Their sense of smell is very acute, and it has been found a good plan to bury a dead crab in the ground infested by them, or pour water with a little oil or turpentine down their burrows, when those not killed will at once vacate.

The mole-cricket, though feeding principally upon vegetation, is really omnivorous, and will take raw beef, grubs, &c., with zest. It has been stated that they are really useful because they do this, but the best authorities give them an unqualified condemnation.

Like their relations, the field-crickets, they are very war-like, and have cannibalistic tendencies, for when an enemy has been vanquished he is sure to be eaten.

Addendum.—Since this paper was read the author has been informed that Mr. Robinson, of Makara, near Wellington, is familiar with the mole cricket, but does not think it has increased in his district during the last two or three years.

Art. XXVII.—On the Cause of the Disappearance of Young Trout from our Streams.

[Read before the Wellington Philosophical Society, 9th January, 1889.]

During the past fifteen years trout-fry have frequently been put into the streams in this district (Palmerston North), but, so far as I am aware, they have never been seen afterwards. Some thought they had been devoured by eels, and others that they had been washed out of the streams by freshes. As it is a subject in which I take considerable interest, and one which has cost many a pound to no purpose, I set myself some twelve months ago to discover, if possible, what was really the matter. It occurred to me that there was little use in examining the streams, or in speculating on the cause of the mischief, and that something more practical would require to

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be done. I had a tank erected, 12ft. long by 30in. wide and 24in. deep, divided into three compartments with movable partitions. The front of this tank or aquarium is of glass, so that I can observe all the movements of the fish; and, although I have not a constant flow of water, there is sufficient to answer my purpose. I observed that in all the streams in this district there are large numbers of minnows (Galaxias attenuatus), which are pretty to look at, and apparently innocent and timid; but, as they take the worm freely, I thought they might just as readily take the young trout. I placed seven of them in the tank, and gave them worms nearly as long as themselves. These they ate greedily. I then gave them dead whitebait, which they ate as freely. My next experiment was with twenty-five live trout six weeks old; and within twelve hours they had all disappeared except one, which may have been hidden among the plants, and so escaped their observation. By this time I was satisfied that they were at least one cause of the mischief, but to make certain I tried once more. I placed two minnows in the tank with fifteen trout nine weeks old; and within half an hour three of the latter had disappeared. I then dissected one of the minnows, and took from it one of the trout, which had been swallowed whole. I may add that the minnows had been well fed before they were placed with the trout; and if they will devour them under these circumstances, we may well understand how readily they will attack them in the streams. There may be other reasons for our want of success in stocking the streams; but, apart from all others, this of itself is sufficient to account for it.

Experience has proved that it will not do to place the young fry in the streams and leave them to take care of themselves, and an important question would be, at what age will they be old enough and strong enough. This I cannot answer definitely. I have had the trout with the minnows when they (the trout) were seven months old, and they seemed to live in harmony. Whether they would do so at an earlier stage I cannot say.

I think if the following plan were adopted we might reasonably look for success: Let the fry be brought from the breeding-ponds, as formerly, when they are, say, four or five weeks old, before they have lost the umbilical sac, for reasons which will be apparent to any one at all acquainted with the subject. Place them in a pond through which there is a constant flow of water, and where other fish cannot get at them. Let them be kept there until they are, say, twelve months old, after which it will be quite safe to turn them into the stream. The pond could be cut out close to the stream from which the water-supply would be taken, and the overflow could go back

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to its former channel. I would have a number of large stones in the bottom of the pond to provide hiding-places, as the trout of all ages seem inclined to lie quiet during the day, and come out at dusk to rove about. While kept in the pond they should be fed regularly.

I have pleasure in adding that I have been greatly indebted to Mr. Ayson, of the Wellington Acclimatization Society, at Masterton, from whom I have received much valuable information, and small parcels of trout for experimental purposes.

Art. XXVIII.—The Distribution and Varieties of the Fresh water Crayfish of New Zealand.

[Read before the Otago Institute, 11th September, 1888.]

Plate X.

For some years past I have been engaged, whenever opportunity offered, in forming a collection of freshwater crayfish from the various parts of New Zealand, with a view of determining exactly how many species were represented, and what varieties of these species, if any, existed. By the assistance of several friends I have succeeded in getting a fairly representative collection from both islands, and I now give the somewhat meagre results that I have arrived at from the examination and comparison of specimens from the various localities.

It will be well first to state briefly what has been previously written on the subject.

Miers, in his catalogue of the stalk- and sessile-eyed Crustacea of New Zealand (pp. 72, 73), published in 1876, gives three species of freshwater crayfish as inhabiting New Zealand—viz., (1) Paranephrops planifrons, White (including under this P. tenuicornis, Dana), (2) P. setosus, Hutton, and (3) P. zealandicus, White.

P. planifrons is well known from many parts of the North Island, and P. setosus from the Avon, in North Canterbury, and from other localities in the South Island; but P. zealandicus does not seem to have been with certainty recognised since it was originally described by White. It was described in 1847, and as I have already stated in a previous paper,* Professor Hutton, who described his P.

[Footnote] * “Trans. N. Z. Inst.,” vol. xv., p. 151.

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setosus in 1873, was not then able to consult White's description of P. zealandicus, or he would probably, he tells me, not have described his as a new species. I have, in my paper already referred to, discussed to some extent the probability of the identity of these two species, but at that time I was unable to give a decisive opinion on the matter, owing to the want of a sufficiently large collection to examine; and it was chiefly with a view of finally settling the question that I undertook the present investigation.

It is somewhat difficult to compare the descriptions of P. setosus and P. zealandicus, as they do not run exactly parallel; the differences, however, have been clearly stated by Miers,* who was able to examine the type-specimens of P. zealandicus in the British Museum, and to compare them with a specimen of P. setosus, Hutton. In speaking of P. zealandicus he says, “This species is certainly distinct from P. setosus, Hutton. In P. zealandicus, of which the type-specimens are in the British Museum collection, the hands are clothed externally with tufts of hair, arranged in longitudinal series, and are armed with spines only on the superior margins; and the sides of the carapace are smooth. In P. setosus there are spines arranged seriately upon the external surface as well as the upper margin of the hand, and the branchial and hepatic regions of the carapace are armed with numerous unequal conical spines.”

I have specimens, from streams at Dunedin, that agree fairly well with the description of P. zealandicus as given in Miers's catalogue; and, though they differ to some extent from typical specimens of P. setosus, the characters in which they differ vary, as I shall show in detail further on, to a large extent according to size and age, even in specimens taken from the same stream, and such a complete series of transitional forms is found that it will, I think, be necessary to combine the two species under the name P. zealandicus, which has priority over P. setosus by many years: but, in accordance with the rule suggested by Professor von Martens, and adopted by Professor Hutton, and by Mr. G. M. Thomson and myself, the name must be written Paranephrops neo-zelanicus.

The differences between specimens of P. planifrons of different ages and localities are quite as great as those between different forms of P. neo-zelanicus; so that, if the latter species were divided, it would be necessary to divide the former also.

The only other reference to two species of Paranephrops from New Zealand besides P. planifrons that I can find is an

[Footnote] * “Ann. and Mag. N. H.,” ser. 4, vol. xv., p. 412.

[Footnote] † See “Trans. N.Z. Inst.,” vol. xvi., p. 187, and vol. xviii., p. 141.

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incidental one by Wood-Mason. Speaking of the parasite (Temnocephala)* found on these crayfish he says, “I have since received from my friend Mr. W. Guise Brittan, of Christchurch, New Zealand, an abundant supply of each of two species of crayfish from the rivers Avon and Waimakariri respectively.” (The italics are mine.)

In consequence of this notice I was exceedingly anxious to get specimens from the Waimakariri to compare with the Avon species, to see whether they differed or not; but for a long time I was unsuccessful. However, in September, 1885, one of my pupils brought me specimens, not, indeed, from the River Waimakariri itself, but from a creek at Rangiora that empties into one of its branches. These specimens, though differing in some respects from the typical specimens of P. setosus, and therein approaching the Dunedin specimens, are not sufficiently distinct to be considered a separate species. I have therefore no doubt that Wood-Mason's specimens all belonged to the one variable species—P. neo-zelanicus.

While examining into the identity of P. setosus and P. zealandicus I have at the same time examined and compared with them specimens of P. planifrons from various localities, and find that most of the points of difference hitherto given break down when a large number of specimens is examined, and that it is exceedingly difficult to find constant characters by which to separate them. At one time I was almost tempted to combine the two species (P. planifrons and P. neo-zelanicus) into one; but, in consideration of the distinctness between extreme forms, I have thought it best to keep them as two species, though with some intermediate specimens it is sometimes hard to decide which species they should be referred to. The various differences will be given in the detailed description further on, but for the sake of greater clearness I will briefly mention some of them here. The squame of the antenna is generally larger in P. planifrons than in P. neo-zelanicus, usually reaching slightly beyond the extremities of the rostrum and of the peduncles of the antennules and antennæ; but this character fails us in some specimens from Wellington and Pelorus Valley, &c. The sides of the carapace in P. planifrons do not, as a rule, bear so many or such well-developed spines as in P. neo-zelanicus; but the general arrangement is much the same, and some specimens of P. planifrons (as, for

[Footnote] * See below, Art. xxix.

[Footnote] † “Ann. and Mag. N. H.,” ser. 4, vol. xv., p. 336.

[Footnote] ‡ He gives the name of one species only, however—viz, Astacoides zealandicus=Paranephrops setosus, Hutton.

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instance, those from Nelson) are very spiny, while many of P. neo-zelanicus have the carapace almost smooth. In P. planifrons, again, the infero-posterior corner of the pleura of the abdominal segments is usually distinctly angular, while it is more or less rounded in P. neo-zelanicus; but this character, again, varies considerably in both species. The character that I have found most useful in distinguishing the two species is in the form, &c., of the great claws. In P. planifrons these are long, and have the basal portion of the propodos (without the fixed finger, that is) usually fully twice as long as the carpus, and generally more than twice as long as broad; and, though it sometimes bears a few scattered hairs, these are never abundant and are not arranged in tufts. In P. neo-zelanicus the propodos is usually somewhat compressed, it is generally less than twice as long as the carpus, and not more than twice as long as broad, and it is always abundantly covered with hairs arranged in tufts. The relative sizes of the different joints vary to a considerable extent; but I have found the abundant hairs in all my specimens of P. neo-zelanicus, and this forms the only character that I have been able to rely upon in all cases to distinguish this species from P. planifrons.

It has generally been stated hitherto that P. planifrons is confined to the North Island and is not found in the South, but is represented there by P. neo-zelanicus. In August, 1883, however, I received from the late Mr. J. C. Gully two very fine specimens of P. planifrons from a stream—the Maitai—at Nelson. It would hence appear that Cook Strait has not proved so great, or, rather, so old a barrier to these crayfish as the mountains in Nelson forming the northern continuation of the Southern Alps. As this point seemed to be of some importance in connection with the geographical distribution of the fauna of New Zealand, and as I was ignorant of the configuration of that part of the South Island, I applied to Professor Hutton for information. With his characteristic kindness and promptness he at once told me that there was no great division (by mountains, that is) between Nelson and Greymouth, but that the first great division would be along the Kaikoura Mountains and across westerly to Mount Franklin, and then down the Spencer Mountains and the Southern Alps; though the part between the Kaikoura Mountains and Mount Franklin is much broken by rivers, some running north and some south. He also told me that several North Island plants extend to Nelson and down the west coast to Westport and Greymouth. Another fact pointing in the same direction is found in the distribution of Armadillo speciosus, a terres-trial isopod. This is known from the North Island (Bay of Islands, Dana, and Wellington, Hutton), and I have specimens

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from Nelson; but I have never heard of it occurring in the southern part of the South Island.

It was therefore to be anticipated that specimens of Paranephrops found north of the dividing-line mentioned by Professor Hutton would, like those from Nelson, belong to P. planifrons rather than to P. neo-zelanicus. To test this I applied to Mr. J. Rutland and Mr. R. Helms, and these gentlemen very kindly supplied me with specimens from Pelorus River and Greymouth respectively. These specimens, though to some extent intermediate, like those from Nelson, are without the characteristic tuft of hairs found in P. neo-zelanicus, and therefore belong, as I had anticipated, to P. planifrons, the North Island species.

The crayfish seem to be very widely distributed over all the different parts of New Zealand. Of P. planifrons I have specimens from Karaka, Manukau Harbour; Puriri Creek, Thames; Lake Roto-iti; Napier; Wellington; Nelson; Pelorus River; and Greymouth: and of P. neo-zelanicus from various streams in North Canterbury, from Oamaru, and from Dunedin. I have also heard of it from Southland and various portions of the interior of Otago, and Mr. G. M. Thomson has taken it in Stewart Island and in the western tributaries of the Waiau, in the south-west part of Otago.

A freshwater crayfish belonging to the same genus as those of New Zealand—Paranephrops—is said to be found in Fiji, and is mentioned by Professor Huxley in “The Crayfish,” p. 313, and also in his paper in the “Proceedings of the Zoological Society,” 1878, p. 770. In “The Crayfish,” p. 313, he states that “considering their wide separation by sea, the amount of resemblance between the New Zealand and the Fiji specimens is very remarkable.” As this fact is of some importance in connection with the question of the origin of the New Zealand fauna, I have in several ways endeavoured to get specimens from Fiji for comparison with those of New Zealand, but as yet I have been unable to hear of any one in Fiji who would collect them for me. It appears that the statement that Paranephrops is found in Fiji rests on two specimens in the British Museum, and I notice that Professor W. Faxon suggests that the locality-labels are perhaps erroneous.*

Before proceeding to give detailed descriptions of P. planifrons and P. neo-zelanicus, I desire to take this opportunity of thanking those friends who have kindly provided me with material—viz., Mr. T. F. Cheeseman, Auckland; Mr. A. Hamilton, Napier; Mr. T. W. Kirk, Wellington; the late Mr. J. C. Gully, Nelson; Mr. J. P. Grossman, Christ-

[Footnote] * “Revision of the Astacidæ,” part i., p. 2 (footnote).

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church; Professor Parker and Mr. T. Butement, Dunedin; Mr. J. Rutland, Pelorus Valley; and Mr, R. Helms, Grey-mouth.

I shall now give a somewhat detailed description of the external characters of P. planifrons, taking one of the Napier specimens as a fairly typical one, and then briefly pointing out the variations found in other specimens. I shall do the same with P. neo-zelanicus, taking a specimen from the River Avon as the type. Further detailed information will also be given in a tabular form in an appendix, and brief diagnoses of the two species are also added. I may explain that I have examined only those external characters that are usually taken for the purpose of distinguishing different species of crayfish, and I have only concerned myself with the New Zealand species of Paranephrop's, and have not compared the genus with other genera of the Potamobiidæ—this comparison will, I hope, be made by Professor Walter Faxon (to whom specimens have been sent) in the second part of his “Revision of the Astacidæ.

Description of Napier Specimen of P. planifrons.

[The section below cannot be correctly rendered as it contains complex formatting. See the image of the page for a more accurate rendering.]

The specimen is a male, 5·26in. in length from the tip of the rostrum to the end of the telson; the greatest breadth is 1·2in.; the length of the antennæ is about 4in., and of the great claws 4·5in. The rostrum is elongate triangular, with raised margins bearing four spines on each side; it is keeled below, and on the keel bears two median spines, which can be seen from below just between the peduncles of the antennules. It will be convenient to represent the spines on the rostrum by the formula 4–4/2, the figures above the line giving the number of spines on the right and left sides respectively, the figure below the line indicating the median spines on the keel below. The carapace is nearly circular in transverse section, the surface somewhat scabrous, most parts covered with very fine hairs placed singly; the spines and tubercles are mentioned below. The short median ridge behind the rostrum begins slightly in front of the posterior termination of the two lateral ridges of the rostrum; it is clearly marked in front, but becomes less distinct posteriorly, and disappears about half-way between its anterior extremity and the cervical groove. At the base of the rostrum on each side are two spines behind the eyes; there is a row of hairs between them and a tuft in front of the anterior spine; from the posterior spine a slight ridge extends backwards about as far as the posterior end of the median ridge. The spines on the carapace may for the sake of convenience of reference be divided into the following arbitrary groups (see Plate X., fig. 2):—

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Paranephrops Palnifrons.—

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(1.)

On the portion of the carapace in front of the cervical groove:

  • Group A, containing the two spines at base of the rostrum on each side.

  • Group B, two spines behind the eyes and below A.

  • Group C, three or four spines on anterior margin of the carapace, near the bases of the antennæ.

  • Group D, two or more spines on the part of the carapace posterior to C, and in front of the cervical groove.

  • Group E, one or two spines below D, and usually on a slight projection of the carapace.

(2.)

On the portion of the carapace behind the cervical groove:

  • Group F, two spines immediately behind the cervical groove, and between it and the branchio-cardiac grooves, which here extend forwards and outwards towards the cervical groove.

  • Group G, four spines close behind the vertical portion of cervical groove below and in front of F.

  • Group H, six or seven spines along the cervical groove where it curves horizontally forwards (below group E).

  • Group J, includes the spines and tubercles on the branchiostegites, excluding those bordering the cervical groove and already enumerated. About six of the more anterior are distinctly spinous, the others gradually degenerate posteriorly into mere tubercles.

The peduncles of the antennæ and antennules both reach about to the end of the rostrum; that of the antenna bears several spines on the under surface of the different joints. The squame of the antenna is large, and reaches rather beyond the end of the rostrum; it is triangular, narrowing anteriorly, and at the end narrowing abruptly to a sharp point; the inner edge is fringed with long setæ, and there is a deep longitudinal groove above. The anterior part of the epistoma, between the bases of the antennules, is broad, triangular, and flat, ending anteriorly in a sharp spine. The great claws are large and long, being about six-sevenths the length of the body. The propodos is not compressed, and its length (excluding the fixed finger) is about twice as great as that of the carpus, and about three times its own width; it widens slightly towards the distal

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end. The whole limb is densely spined: the basos has one spine on the inner margin; the ischios has a few on the inner margin, and one or two indistinctly marked on the outer margin; the meros has two irregular rows on the inner margin, and one row on the outer margin, and one spine on each side of the hinge; the carpus is spined all round, with a slight groove above, between two longitudinal rows; the propodos is densely spined in longitudinal rows, the largest spines being on the upper surface and the inner margin, and in one row of about six on the lower surface; there are two very regular rows on the outer margin, extending right to the end of the fixed finger. Both fingers are very spinous, inner margins with rounded teeth and a few hairs, the fingers ending in incurving spines. The pleura of the abdominal segments have the infero-posterior corner distinctly angled, the anterior edge being longer and more convex than the posterior, which, though slightly sinuous, scarcely curves forward; the anterior edge alone fringed with setæ.

The specimen I have described is the largest of P. planifrons that I have seen. I have two others from Nelson, 4·8in. long, and others from Lake Roto-iti, 4·15in. and 4in. long. On the other hand we may have mature specimens very much smaller: thus I have a female bearing eggs, from the Thames, only 2·4in. long, and another, from Wellington, 2·5in. From the measurements given in the table below it will be seen that the proportion of the greatest breadth of the carapace to the length varies to some extent, but is almost always less than one-fourth the length. When seen in dorsal view the sides of the branchiostegites are nearly parallel, so that the carapace is about the same width throughout the whole length of the branchiostegites. The sides, however, sometimes bulge slightly in the centre, but not to so great an extent as the Avon and Heathcote specimens of P. neo-zelanicus. (See Plate X., fig. 1, and compare it with fig. 1a.) The number of teeth on the rostrum varies very greatly, and very often differs on the two sides; the median teeth below are sometimes entirely absent, as in the Pelorus River specimens, where they are present in one specimen only. The spines, too, vary in distinctness, being very sharp and distinct in the Nelson and Greymouth specimens, but blunt and more or less rounded at the end in those from Lake Roto-iti. The rostrum is frequently depressed, as in the Napier specimen, but, again, is often quite horizontal, or only very slightly depressed. The median ridge on the carapace, behind the rostrum, varies much in length and distinctness, but usually does not extend so far back as in P. neo-zelanicus. With regard to the spines on the carapace, it must be remembered that the groups into which I have divided them, though useful

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for easy reference, are purely arbitrary, and may not always be clearly distinguished. The spines often vary both in number and position on the two sides of the same specimen. In some specimens the spines are almost entirely absent, so that the whole of the carapace is nearly smooth; but usually some of the groups are represented, if not by spines, by small tubercles corresponding in position to the spines in other specimens. I have tabulated the number of spines of each group found in various specimens, and, though I need not give the tables, I can summarise some of the results here. Group A contains only two spines, and is invariably present; group B is frequently altogether absent, but may contain several spines, as in the Nelson specimens, extending into group D and group K, mentioned below; group C is usually represented, but often only by very small spines; group D is often absent in small specimens, but may contain as many as six spines, extending right back to the cervical groove; group E is seldom entirely absent, and never contains more than two spines; group F is often absent, and the spines in it are never large; group G is one of the most constant, and contains some of the largest spines, it is seldom entirely absent; group H, again, is also usually represented, though the number of spines varies very much, and they are sometimes very small and close together, so as to form only a row of more or less spinous tubercles; group J, including the spines and tubercles on the branchiostegites, is very variable—sometimes the spines are entirely absent, so that this part of the carapace is quite smooth, at other times the spines are represented by slight roughness only, but, again, as in the Nelson specimen, the whole of the branchiostegite may be thickly covered with well-developed spines. In the specimen from Nelson, two other groups, present in many specimens of P. neo-zelanicus, but not represented in other specimens of P. planifrons, are noticeable: they are, group K, containing 4–5 spines in front of the cervical groove and behind group B; and group L, containing two or three small spines on the cardiac portion of the carapace, usually by the sides of the branchio-cardiac grooves. (See Plate X. fig. 2a.) In this Nelson specimen the number of spines in each group is much greater than usual, and they run into one another so much that, as in some specimens of P. neo-zelanicus, it is difficult to distinguish them into the different groups. In the Lake Roto-iti specimens the spines are usually more or less blunt, and often degenerate into tubercles.

The squame of the antenna sometimes reaches only as far as the extremity of the rostrum, instead of beyond it as in the Napier specimen. The inner edge is generally straight in the centre, or even slightly concave; but sometimes more convex, as it usually is in P. neo-zelanicus. Towards the end it often

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narrows somewhat abruptly, so that a portion of the margin here is very convex; I have never, however, seen it produced into a distinct point, as shown in Dana's figure of P. tenuicornis, and think this must be due to an exaggeration on the part of the artist. (Compare figs. 3 and 4 of Plate X.) The spines on the under surface of the joints of the peduncle of the antenna are often entirely absent in small specimens, even though sexually mature. The length of the antenna varies considerably (see table below): it may sometimes, as in Nelson specimens, be greater than that of the body itself. The great claws, again, vary very greatly, both in proportion to the body and in the shape and relative size of the different joints. Large, well-developed forms have the propodos long and thick (i.e., not compressed), and are easily distinguished from those of P. neo-zelanious; but in others the propodos is somewhat compressed, and is not so long in proportion to its breadth, thus approximating in appearance to those of P. neo-zelanicus. In the large specimens the propodos is often fully three times as long as broad, but in some specimens from the Thames, Greymouth, &c., it is not more than twice as long as broad, and in these it does not widen distally as it usually does in the others. In the same way the spines on the great claws vary to quite as great an extent as those on the carapace, but it would be tedious to enter into detail. In the Lake Roto-iti specimens those on the propodos are nearly all more or less tubercular, instead of being distinctly spinous, as is usually the case. The propodos, especially in the smaller specimens, often bears a few scattered hairs, but these are never arranged in tufts as in P. neo-zelanicus.

The distinctness of the infero-posterior angle of the abdominal pleura also varies very considerably, and it is sometimes quite rounded, as in P. neo-zelanicus.

Description of Avon Specimen of P. neo-zelanicus.

[The section below cannot be correctly rendered as it contains complex formatting. See the image of the page for a more accurate rendering.]

As this specimen agrees in many respects with the one of P. planifrons already described, I shall only give those points in which it differs. The length of the body is 4·85in., greatest breadth 1·2in., length of antennæ 3·5in., of great claws 3·5in. The branchiostegites bulge considerably in the centre, so that the breadth here is much greater than in front of the cervical groove. The rostrum has 4–4/1 as the formula for its spines, and is only slightly depressed. The median ridge behind the rostrum begins on a level with the anterior of the two spines at the side, and extends about three-fourths of the way back to the cervical groove. The spines on the carapace are very numerous, several of the groups running into one another. They may be briefly described as follows, using the same

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groups as in P. planifrons: Group A, two, as usual; B, three or four, irregularly placed; C, five, but not arranged so regularly on the margin of the carapace as in P. planifrons; D, six, extending right back to the cervical groove, and running anteriorly into C; E, one, situated on slight prominence; F, two; G, four or five, very strong, extending into H; H, a row of about seven, extending along the under margin of the groove; J, the whole branchiostegite covered with well-developed spines, all sharp and distinct except those on the lower portions, which are rubbed by the legs and are rounded at the end—the spines extend much further up than is usual in P. planifrons, reaching almost to the branchio - cardiac grooves; K, a group of about eight well-marked spines; L, two or three small spines along the branchio-cardiac groove on each side. The squame of the antenna scarcely reaches beyond the extremity of the rostrum, and has its inner margin more convex than is usually the case in P. planifrons. The anterior portion of the epistoma is quite narrow, and ends anteriorly in a sharp spine. The great claws are much shorter and stouter than in extreme forms of P. planifrons, and have the propodos and the fingers thiekly covered with dense tufts of hairs, chiefly arranged in longitudinal rows. The ischios and meros are somewhat laterally compressed, so that it will be convenient in describing the spines on them to speak of the upper and under edges and the outer and inner sides; the carpus and propodos are more or less vertically compressed, so that we can distinguish here the outer and inner edges and the upper and under sides. The spines on the great claws are then arranged as follows:—

Ischios—Upper edge, two blunt spines.

Under edge, two sharp spines.

MerosUpper edge, one row dividing into two at the end, where there are also a few spines irregularly placed.

Under edge, two diverging rows, containing four to six spines each; one large spine at distal end between the two rows, and others placed irregularly.

The outer and inner sides of these joints without spines.

Carpus—Spined all round, the largest on the outer and inner edges; on the upper side the central portion is flat and free from spines.

Propodos—Inner edge, a row of four strong spines.

Outer edge, two rows, containing about twelve spines each, extending right along to the end of the fixed finger.

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Upper side, various spines, chiefly arranged in two longitudinal rows.

Under side, spines chiefly arranged in two longitudinal rows; strong spines in the centre.

The fingers end in strong incurved spines, inner margins with three or four rounded prominences. The propodos (without the fixed finger) is one and a half times as long as the carpus, and about twice as long as broad. The pleura of the abdominal segments is quite rounded below, and has setæ both on anterior and posterior margins. (See Plate X., fig. 2a.)

All the parts I have thus described are subject to much variation, as in P. planifrons, and I need not go over each in detail, but only mention those in which this species sometimes differs from P. planifrons. The bulging of the branchiostegites is only found in the specimens from the Avon and Heathcote; the others have the sides straight as in P. planifrons. The epistoma is often narrow, but is sometimes broad, flat, and triangular, as in P. planifrons. The spines on the sides of the carapace vary very greatly: in large specimens, especially those from the Avon and Heathcote, they are very numerous and prominent; but in others, from Rangiora and Dunedin, only a few are represented, and the greater part is quite smooth. Some of these specimens would correspond fairly well with the description of P. zealandicus, White, as given in Miers's catalogue. The relative lengths of the joints of the great claws vary a good deal, as in P. planifrons; but these limbs are usually shorter and broader than in that species. The pleura of the abdominal segments often have the infero-posterior angle more pointed than in the Avon specimens, thus approaching P. planifrons. The large specimen in the Otago Museum, labelled P. setosus in Professor Hutton's handwriting, is the largest I have seen, being 6·3in. long; the sides of the branchiostegites are quite straight; the spines on the carapace, though numerous and well marked, are all rounded at the end, so as to be almost tuberculiform; the propodos of the great claws is very little compressed, and somewhat resembles that of P. planifrons, though stouter; and the upper margin bears very few spines, the tufts of hairs arising out of small tubercles instead.

In both species the females, especially when bearing eggs, have the abdomen wider than it is in the male, but beyond this I have noticed no other differences between the sexes.

I append brief diagnoses of the two species, with the synonymy so far as it is known to me.

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Paranephrops Planifrons.

Paranephrops planifrons.

White, “Zool. Miscel.,” p. 79 (1842).

Dieffenb., “Voy. New Zealand,” ii., p. 267 (1843).

Miers, “Zool. ‘Erebus’ and ‘Terror,’” Crust.,” p. 4, pl. iii., fig. 1 (1874); “Cat. N.Z. Crust.,” p. 72 (1876).

Huxley, “Proc. Zool. Soc.,” 1878, p. 770.

Paranephrops tenuicornis.

Dana, “U.S. Exped.,” xiii., Crust., part i., p. 527, pl. xxxiii., fig. 4 (1852).

Basal scale of antennæ large, narrowing abruptly anteriorly, with deep groove above, reaching, as far as or beyond the extremities of the rostrum and of the peduncles of the antennæ and antennules. Carapace nearly cylindrical, of same width throughout whole length of the branchiostegites, being a little less than one-fourth the total length of body; smooth, or with small tubercles on sides of branchiostegites, and spines along the cervical groove and elsewhere; two spines on each side of the base of the rostrum. Bostrum elongate, triangular, sometimes depressed, margins raised and usually with four teeth on each side, under surface keeled and usually with two teeth. Median ridge behind the rostrum clearly marked in front, arising slightly in front of the two lateral ridges of the rostrum, and reaching about half-way from its anterior extremity to the cervical groove, disappearing gradually. Anterior portion of the epistoma triangular, flat, narrowing anteriorly, and ending in a sharp spine. Great claws long, slender, propodos (without fixed finger) about twice as long as the carpus and about two and a half times as long as broad, whole limb densely spined; spines on propodos arranged more or less regularly in longitudinal rows, and with occasionally a few scattered hairs. Pleura of abdominal segments rather pointed at the infero-posterior angle, anterior edge longer and more convex than the posterior and fringed with setæ, posterior edge sinuous and scarcely curving forwards.

Length of largest specimen, 5·25in.

Habitat. North Island generally, and the north-western portion of the South Island as far south as Greymouth.

Paranephrops neo-zelanicus.

Astacus zealandicus.

White, “Proc. Zool. Soc.,” p. 123 (1847); “Ann. and Mag. Nat. Hist.” (ser. 2), i., p. 225 (1848).

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Paranephrops zealandicus.

Miers, “Zool. ‘Erebus’ and ‘Terror,’” Crust., p. 4, pl. ii., fig. 2 (1874); “Cat. N.Z. Crust.,” p. 73 (1876); “Ann. and Mag. Nat. Hist.” (ser. 4), xv., p. 412 (1876); “Trans. N.Z. Inst.,” ix., p. 475 (1877).

Chilton, “Trans. N.Z. Inst.,” xv., p. 151 (1883).

Astacoides zealandicus.

Wood-Mason, “Ann. and Mag. Nat. Hist.” (ser. 4), xv., p. 336 (1876).

Paranephrops setosus.

Hutton, “Ann. and Mag. Nat. Hist.” (ser. 4), xii., p. 402 (1873).

Miers, “Cat. N.Z. Crust.,” p. 72 (1876); “Ann. and Mag. Nat. Hist.” (ser. 4), xv., p. 412 (1876); “Trans. N.Z. Inst.,” ix., p. 475 (1877).

Chilton, “Trans. N.Z. Inst.,” xv., p. 150 (1883).

Basal scale of antennæ like that of P. planifrons, but not narrowing so abruptly, and extending only to the end of the rostrum. Carapace nearly cylindrical, greatest breadth generally a little less than one-fourth the length, of the same width throughout whole length of the branchiostegite, or bulging in centre; carapace nearly smooth, or with spines along the cervical groove and on the branchiostegite and elsewhere, spines usually more numerous than in P. planifrons; two spines on each side of the base of the rostrum. Rostrum elongate, triangular, sometimes depressed, margins raised and usually with four teeth on each side, under surface keeled and usually with two teeth. Median ridge behind rostrum arising on level with the first of the two spines at the base of the rostrum and extending backwards three-fourths of the distance to the cervical groove. Anterior portion of epistoma flat and triangular, or narrow, ending anteriorly in a sharp spine. Great claws stout, propodos usually compressed, one and a half times as long as the carpus and nearly twice as long as broad, both sides covered with small tufts of hair and with stout spines arranged chiefly in longitudinal rows. Pleura of abdominal segments usually rounded below, anterior edge longer than the posterior, which curves forward, both edges fringed with setæ.

Length of largest specimen, 6·3in.

Habitat. South Island generally, excepting north-western portion; Stewart Island.

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Table Of Measurements, etc., of Different Specimens.
Description of Specimen. Length in Inches. Greatest Breadth in Inches. Length of Antennæ in Inches. Length of Great Claws in Inches. Spines on Rostrum.
Paranephrops planifrons.
Napier specimen No. 1, ♂ 5.25 1.2 4 4.5 4—4/2
" " No. 2, ♀ 4.7 1.1 Broken 3.2 5—4/3
Roto-iti " No. 1, ♂ 4.15 1 2.75 3 4—4/1
" " No. 2, ♂ 4 1 3.5 3 3—3/2
Manukau " No. 1, ♀ 3.25 0.7 3 2.25 3—3/2
" " No. 2, ♂ 2.85 0.55 2.4 2 4—4/2
Nelson " No. 1, ♂ 4.8 1.1 5.3 4.1 4—5/1
" " No. 2, ♂ 4.8 1.1 4.6 4.1 Broken
Thames " No. 1, ♂ 3 0.6 2.75 2.4 3—2/1
" " No. 2, ♀ 2.4 0.5 1.9 1.6 3—3/1
Wellington specimen No. 1, ♀ 2.5 0.5 1.7 Wanting 6—5/2
Greymouth specimen No. 1, ♀ 3.5 0.8 3.2 2.4 4—4/2
Pelorus Valley specimen No. 1, ♀ 3 0.6 2.5 2 5—4/0
Paranephrops neo-zelanicus.
River Avon specimen No. 1, ♂ 4.85 1.2 3.5 3.5 4—4/1
River Avon specimen No. 2, ♂ 5.8 1.5 4 4.25 5—5/3
River Avon specimen No. 3, young ♀ 2.2 0.45 1.7 1.35 6—3/1
River Heathcote specimen No. 1, ♀ 3.6 0.85 2.75 2.25 4—5/2
Rangiora specimen No. 1, ♂ 3.9 0.9 3 2.8 4—4/1
Oamaru specimen No. 1, young ♂ 2.5 0.5 1.6 1.7 5—6/1
Dunedin specimen No. 1, ♀ 2.3 0.5 1.9 1.7 5—4/0
Dunedin specimen No. 2 6.3 1.5 4.5 5 5—6/2
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In the above tables I have given only a small selection of the specimens that I have examined and measured.

Description of Plate X.

Fig. 1. Parancphrops planifrons (Napier spécimen); carapace from above.

Fig. 2. The same; side view, to show arrangement of spines, &c., on carapace.

Fig. 3. The same; squame of antenna.

Fig. 4. Squame of antenna of Paranephrops tenuicornis, Dana (after Dana).*

Fig. 1a. Paranephrops neo-zelanicus (Avon specimen); carapace from above.

Fig. 2a. The same; side view, to show arrangement of the spines, &c., on carapace.

Note.—All the drawings are semi-diagrammatic.

Art. XXIX.—Note on the Parasite (Temnocephala) found on the Freshwater Crayfish of New Zealand.

[Read before the Otago Institute, 11th September, 1888.]

On both species of Paranephrops inhabiting New Zealand an ecto-parasite is found belonging to the genus Temnocephala, an aberrant monogenetic trematode. This has been mentioned by Wood-Mason, who referred it to the typical species T. chilensis, Gay. Specimens were afterwards sent to Dr. W. A. Haswell, of Sydney, who has lately published a paper on the genus, and he has given it the name T. novæ-zealandiæ. Similar species are found on other freshwater crayfish of Australia and Tasmania, each having its peculiar species of parasite, viz.,—

T. fasciata, on Astacopsis serratus; streams of New South Wales.

T. quadricornis, on Astacopsis franklinii; northern rivers of Tasmania.

T. minor, on Astacopsis bicarinatus; streams of New South Wales.

[Footnote] * This is taken from a tracing kindly made for me by Professor Hutton from Dana's “Atlas,” in the Canterbury Museum.

[Footnote] † “Ann and Mag. N.H.,” ser. 4, xv., p. 336.

[Footnote] ‡“Q. J. of Micr. Science,” xxviii., part 2, p. 279.

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The New Zealand species I have found most abundant on specimens of Paranephrops neo-zelanicus from the Avon and Heathcote; but I have also found it on P. planifrons from Nelson, and I have seen its egg-cases on specimens of the same species from Napier and Greymouth. It is also found on Dunedin specimens of P. neo-zelanicus, but I have not noticed it on specimens of P. planifrons from Roto-iti, the Thames, and Manukau Harbour.

It should perhaps rather be called a commensal than a parasite, for it can scarcely derive any direct nourishment from the hard exoskeleton of its host: according to Haswell, it lives on small Amphipoda, and it is certainly capable of living for months away from the host, as is shown by the following fact: On the 14th September, 1885, some specimens of Paranephrops neo-zelanicus were brought to me with numerous specimens of Temnocephala novæ-zealandiæ adhering to them. I kept the crayfish alive in a glass jar till the 16th, when I put them in spirit, and during this time some of the Temnocephala detached themselves and moved on to some watercress and river-weed in the jar, and here some of them continued to live until the 16th January, 1886, just four months after they had left the crayfish. The specimen seen on this date appeared quite healthy and vigorous; but I lost sight of it, and did not see it again after that day.

Art. XXX.—On some Gall-producing Insects in New Zealand.

[Read before the Wellington Philosophical Society, 17th November, 1888.]

Plates XI. and XII.

A Common plant in gardens in this country is a native shrub—Olearia furfuracea—usually known to settlers by the name of aké-aké, though the true Maori name is aké-piro. It is a somewhat straggling bush with light-green leaves, the under sides of which are whitish; the leaves much “crimped.” The flowers are small, yellowish, appearing in autumn, and have a faint scent resembling that of the lilac. The plant has no particular pretensions to beauty, but it grows fast to some ten or twelve feet in height, and is useful enough as shelter in a garden.

This Olearia is much subject to the attacks of a couple of minute insects, which, though they belong to two quite

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different families of the class Insecta, the Hymenoptera, and the Diptera, seem to have made common cause against the plant, and live in close alliance at its expense. A good deal of the straggling nature and ungraceful appearance of the shrub is due to their attacks, and doubtless if one could insure freedom from them the Olearia, might be made much more ornamental than it is. Of these two insects, one, the hymenopter, preys apparently only on the buds and young shoots; the other infests both buds and leaves.

The “galls” produced on the plant are of two kinds. The one affecting the young shoots and buds has the appearance of large excrescences formed round the axils of the twigs, as if in those spots an abnormally large number of shoots had begun to grow out, and, having their growth suddenly arrested, had coalesced in an irregular mass, their stunted leaves crushed up and crowded together. Examples of these are shown in Plate XI., fig. 1, and Plate XII., fig. 1. It will be observed that there is a slight difference between these two, the leaflets in one being much smaller and more crowded than in the other. My experience has been that in the larger one (Plate XII.) only the dipterous insect lives; in the smaller one (Plate XI.) mostly the hymenopterous, but frequently, together with it, the dipteron also. A section of either of these galls will show (as in Plate XI., fig.2) a colony of insects, in the pupa or in the larva stages, living in cells within it. The differences between the two insects may be easily seen by the larger size of the dipteron and therefore of its cell, independently of the differences of colour given below.

The other kind of gall is exclusively the work of the dipteron, and takes the form of blisters on the leaves, as shown in Plate XII., fig. 1, and in section, fig. 1a. When the perfect insect is ready to emerge it breaks a hole through the leaf, and the pupa thrusts itself out for about half its length before the fly emerges, as shown in the figure.

Of these two galls the last, on the leaves, would not probably be hurtful; the other, which arrests and deforms the growth of the young shoots, must exercise a baneful effect upon the vigour of the plant.

The two insects appear to go through their transformations and perform their work at the same periods of the year. The eggs are laid about October, and the larvæ emerge from them in a week or ten days. The larvæ seem to change to pupæ at different intervals—sometimes in early summer, sometimes not until the following spring. The perfect flies emerge about October, and probably, on any particular shrub, all about the same time. Procreation takes place immediately. I have seen a male and a female emerge from a gall almost at the same moment, and five minutes afterwards copulate.

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The following descriptions of these insects are offered:—

Order. Hymenoptera.
Sub-order. Terebrantia.
Family. Chalcididæ
Genus Eurytoma.

Eurytoma oleariæ (Gall-fly of Ake-piro). Plate XI., figs. 116.

Insects inhabiting in the larval and pupal states, in colonies, excrescences and abnormal growths (galls) (figs. 1, 2) on the twigs of Olearia furfuracea. The galls are probably not produced by themselves, but by a dipterous insect. (See below.)

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Larva (fig. 3) about 1/18in. in length, grub-like, fleshy, yellowish; no true legs, but a number of very obscure tubercles; the head (fig. 4) exhibits a convoluted ring with two conical processes within it. On each joint of the body there are two minute circular spiracles (fig. 4).

Pupa (fig. 5) black, exhibiting the immature organs of the imago. The pupa is enclosed in a hard, grey case (fig. 5a), which has all the appearance of the dried larval skin. As coarctate pupæ are not, seemingly, found amongst the Hymenoptera, this case must be taken as an exceedingly closely-woven hard cocoon.

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The perfect fly (fig. 6) is about 1/14in. long; colour black, covered with short, fine, grey hairs; antennæ black; legs yellow; wings dark-grey. The head is transverse; eyes large; palpi short; thorax thick; mesothorax large and somewhat elevated; scutellum small. Abdomen (fig. 13) apparently composed of three parts—a short peduncle, a median cylindrical portion, and an oval hinder region with six or seven segments. The ovipositor of the female and the penis of the male are not usually exserted. Antennæ of both sexes (fig. 7, female; fig. 8, male) with twelve joints, of which the first two are very short, the third much the longest, the remaining nine sub-equal, each slightly dilated at the tip; all the joints except the two first hairy. The antennæ of both sexes are very similar: that of the female may be distinguished, perhaps, by being proportionately shorter than that of the male, and the joints after the third rounder. Feet (fig. 9) slender; the femur only moderately thick; the tibia dilated at the tip and bearing a spur; tarsus of five joints. The spur of the tibia on the two front legs (fig. 10) is peculiarly large, apparently cleft in the middle, with serrated edges; and the first joint of the tarsus has a distinct comb of stiff bristles on its inner side. The spur on the tibiæ of the other pairs of legs is a simple spine (fig. 11), and the tarsus bears no comb. Forewings (fig. 12) hairy, with very few veins; the sub-costal and anal

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diverge almost at once, and extend a little within the margins for about half the length of the wing; at rather more than half their own length a conspicuous cross-vein unites them, and forms thus a triangular basal cell. The hind-wing has only one vein on the surface, the sub-costal extending for half its length and terminating at the two hooks on the edge. Both wings have faint patches of dark-grey on the surface. The exserted female ovipositor (fig. 14) has a somewhat thick cylindrical base, with a long, slender, curved tube, ending in a slightly-dilated bulb with three or four spines. The penis of the male (fig. 15) is long, cylindrical, with an oval terminal bulb, at the base of which is a ring of spines. The spermatozoa, (fig. 16) are about 1/6000in. long; they are wonderfully agile in their motions, and in the specimens observed retained their vitality for more than half an hour after extraction from the male insect.

This insect has been placed here in the genus Eurytoma of the family Chalcididæ, as it seems to agree better with that than any other, although not entirely satisfying the conditions. The veining of the wings appears to be more like that of some Cynipidæ, especially in the triangular basal cell; but the simple form of the abdomen removes it from that family, and the presence of the distinct segment between the peduncle and the true abdominal region approaches somewhat to the Ichneumonidæ. Eurytama and its allied genera seem, indeed, to hold an intermediate position between the two families, and on this account the present insect has been assigned to that genus.

A point of importance remains to be considered. The Chalcididæ are not usually phytophagous, gall-producing insects, but parasitic on other flies; and it has always been a matter of doubt whether any of them depart from the rule. A species of Eurytoma is found to do much damage to wheat in America, producing on the stems galls which weaken and destroy the plant; yet it is not certain whether this fly (Eurytoma hordei) may perhaps not be only parasitic on a larva of Cecidomyia, and that this last larva may not be the real gall-producer. In the present case the galls of Olearia contain, as above stated, dipterous flies (described below), and these are Cecidomyia. Our Eurytoma may thus be merely a “messmate,” to use Van Beneden's term, the dipteron being the real plant-enemy. That it is not a true “parasite” seems certain, as, although its larvæ and pupæ are found mixed indiscriminately with those of the Cecidomyia, they are in separate cells, and the Diptera in the leaf-blisters are never infested by them. On the whole, I incline to the belief that the Cecidomyia produces the galls on the twigs, and the Eurytoma takes advantage of them as a residence.

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Order. Diptera.
Sub-Order. Ovipara.
Family. Cecidomyidæ
Genus Cecidomyia.

Cecidomyia olearæ (Blister-fly of Ake-piro). Plate XII., figs. 113.

Insects inhabiting, in colonies, excrescences produced by the larvæ on the young shoots of Olearia furfuracea; or, singly, blisters produced by the larvæ in the leaves of the same plant (figs. 1, 1a, 1b).

The eggs (figs. 2, 3) are elongated, pointed, red in colour, laid in bundles on the young shoots, usually in or near an axil.

Larva (fig. 4) white, becoming yellow before transformation; elongated, sluglike, footless; the head (fig. 5) has a simple flattish front with two curved claw-like processes, and two others, conical (perhaps rudimentary antennæ). There are only two spiracles, simple orifices, placed on the last segment of the body.

Pupa (fig. 6) naked; head-region black, abdomen red with blackish bands; immature wings and feet noticeable. On the head are four or five shortish bristles.

The perfect fly (fig. 7) is elongated and slender; head and thorax dark-red with large black patches; abdomen dark-red with black spots; legs dark-brown. The whole body and legs are covered with short hairs and with a number of black scales (fig. 13), pedunculate, something like those of Lepidoptera; these scales give the appearance of black bands to the abdomen—they are exceedingly-loose, and apt to fall off at the least touch. The head is transverse; eyes conspicuous, almost covering the head; palpi long, four- (or five-?) jointed. Antennæ (fig. 11) in both sexes of fourteen joints, of which the first two are very short, the rest ovate and sub-equal, with hairs on each; in the female the last twelve joints are separated by short peduncles, which are not apparent in the male. Legs very long and slender (figs. 7, .12); the tarsi, five-jointed, the first joint being very small. Wings (fig. 10) grey, with many short hairs on the surface and a fringe of long hairs on the edge; veins few and not anastomosed; the costal vein extends to the tip and meets the second longitudinal, the subcostal extending to about two-thirds of the length of the wing; the third longitudinal reaches the posterior margin at about half its length, and sends off a branch which extends nearly to the margin between it and the second longitudinal, Haltere (fig. 10) conspicuously long, with a large head. Abdomen of female ending in several short lobes, slightly turned

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upwards (fig. 7); at rest, these are folded together (fig. 8); when opened (fig. 8a) two are long, cornute with sharp ends, and four others, shorter and tubercular, enclose a short cylindrical ovipositor. Abdomen of male ending (fig. 9) in two lobes; when exserted (fig. 9a) the penis is thick, cylindrical, somewhat dilated at the tip.

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Length of the body about 1/9in.; length of legs about ⅕in.

In the venation of the wings this insect belongs to the true genus Cecidomyia, as defined by Osten-Sacken. In the genus Diplosis, which is near it, the second longitudinal vein curves downwards and reaches the margin of the wing below the tip. As regards specific distinctions, I have not sufficient material for complete comparison: possibly the presence of the curious and very loosely-attached black scales on the body may be a differentiating character.

Index to Plates XI. and XII.
Plate XI.—Eurytoma oleariæ.
Fig. 1. Gall on twig of Olearia furfuracea Reduced
Fig. 2. Section of ditto, showing enclosed insects.
Fig. 3. Larva × 12
Fig. 4. Head of ditto × 40
Fig. 5. Pupa extracted from case × 10
Fig. 5a. Pupa-case.
Fig. 6. Perfect fly × 10
Fig. 7. Antenna of male × 40
Fig. 8. Antenna of female × 40
Fig. 9. Foot × 40
Fig. 10. Spur on tibia and first joint of tarsus of front legs × 40
Fig. 11. Spur of tibia and first joint of tarsus of hind legs × 40
Fig. 12. Wings × 15
Fig. 13. Abdomen × 15
Fig. 14. Ovipositor of female × 30
Fig. 15. Penis of male × 30
Fig. 16. Spermatozoa of male × 1,000
Plate XII.—Cecidomyia oleariæ.
Fig. 1. Gall on twig and blisters on leaf Natural size
Fig. 1a. Section of leaf-blister.
Fig. 1b Section of gall.
Fig. 2. Bundle of eggs on young shoot Slightly enlarged
Fig. 3. Eggs × 10
Fig. 4. Larva × 10
Fig. 5. Head of larva × 40
Fig. 6. Pupa × 10
Fig. 7. Perfect fly, female × 10
Fig. 8. End of abdomen of female, at rest × 20
Fig. 8a. Ditto, open × 20
Fig. 9. End of abdomen of male, at rest × 20
Fig. 9a. Ditto, penis exserted × 20
Fig. 10. Wing and haltere × 10
Fig. 11. Antenna of female × 25
Fig. 12. Foot × 10
Fig. 13. Scales × 350
Picture icon

Eurytoma Oleariæ.

Picture icon

Cecidomyia Oleariæ.

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Art. XXXI.—Notes on, and recent Additions to, the New Zealand Crustacean Fauna.

[Read before the Otago Institute, 8th November, 1887.]

Plates XIII. and XIV.

The notes in this paper serve partly to extend the range of many species hitherto recorded from only one or two localities in the colony; partly to call attention to descriptions of species new to our lists, but which have been described in foreign publications since the issue of the “critical list”* drawn up b