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Volume 25, 1892

II.—Botany.

Art. XXXI.—On Heterostyled Trimorphic Flowers in the New Zealand Fuchsias, with Notes on the Distinctive Characters of the Species.

[Read before the Wellington Philosophical Society, 18th January, 1893.]

Plate XIX.

Exactly a century ago it was observed by Sprengel that the European water-violet (Hottonia palustris, Linn.) produced flowers of different forms on different plants; in one form the pistil was more than twice the length of the pistil of the other. Although convinced that the phenomenon was not accidental, he was unable to discover any reason for its occurrence, and nearly seventy years elapsed before light was thrown on the subject. It is now well known to be a contrivance to insure fertilisation by means of pollen obtained from flowers of another plant, and it has been proved by experiment that the number of perfect seeds in each capsule thus fertilised is much greater than when pollen is applied from the same plant, or from the same form of flower. Pollen from the anthers of either form of flower must be applied to the stigma of the other in order to obtain the most advantageous results.

Flowers of this kind are said to be “heterostyled”: but, inasmuch as the difference in the length of the style is often correlated with differences in the length of the stamens, the size of the pollen-grains, and the size of the flower, &c., the late Professor Asa Gray suggested that the term was not sufficiently expressive, and proposed to substitute “heterogone” or “heterogonous”; but, notwithstanding the greater comprehensiveness of the latter term, it has not been generally adopted.

Mere difference in the length of the style or stamens, or both, is not of itself sufficient to render a plant heterostyled; there must be a reciprocal relationship between the pollen of one form of flower and the stigma of the other: this may or may not be accompanied by a difference in the pollen and

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sometimes in the stigma. On the other hand, heterostyled flowers may not exhibit any great difference in the length of either style or stamens.

Hottonia palustris exhibits only two forms of flowers, and therefore belongs to the group of heterostyled dimorphic plants. In Lythrum, Oxalis, and one or two other genera heterostyled trimorphic flowers are developed: in each form there are two sets of stamens, and the style varies in length reciprocally with the stamens, the long-styled form having the shortest stamens, and the short-styled form the longest stamens; one set of stamens in each form is of the same length as a set in one of the other forms. No pistil can be fully fertilised except by pollen from stamens corresponding to the length of its style, but the pistil of either form may be fertilised by pollen from one or both the other forms.

The arrangements for cross-fertilisation in the New Zealand species of Fuchsia are much less complicated than in Lythrum or Oxalis, and combine with heterostyled trimorphism a marked tendency to unisexuality, the long-styled form in each species being practically a female flower, although in some instances capable of self-fertilisation.*

The variation in the form of the flowers of the New Zealand fuchsias has been long recognised, although even yet it can scarcely be said to be fully understood. Sir Joseph Hooker, under the description of Fuchsia excorticata, in the “Flora Nov.-Zel.,” volume i., page 56 (1853), remarks, “The stamens vary much in length, being sometimes quite included”; and was so much impressed by the short-styled form of F. procumbens that he was led to consider it a distinct species, and described it as such under the name of F. kirkii. After pointing out that it was impossible to distinguish the two plants by the leaves alone, he adds, “In the flowers they differ widely…. At first I was inclined to think that these differences might be sexual; but I should rather regard them as diagnostic of two representative species that possibly had a comparatively recent origin.”†dagger Mr. G. M. Thomson detected two forms of flowers, one of which he rightly stated to be hermaphrodite in structure but pistillate in function.Tdagger Unfortunately, with other southern botanists, he failed to distinguish between F. colensoi and F. procumbens, and consequently has no distinct reference to the heterostyled flowers of the latter.

All the New Zealand species agree in having alternate leaves and axillary solitary flowers, although in F.excorti-

[Footnote] * It it were not for the two forms of hermaphrodite flowers, the New Zealand fuchsias might be termed gynodiœcious.

[Footnote] † Ic. Pl., 3rd ser., i., 67.

[Footnote] † Trans. N.Z. Inst., vol. xiii. (1880), p. 264.

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cata the flowers are sometimes aggregated on very short branchlets, with undeveloped internodes. They further agree in having deep-blue dry pollen, bound together with extremely delicate threads, which are slightly viscid,* and penetrate the mass in all directions, so that the pollen-grains readily adhere to the feathers of birds which frequent the trees for the sake of the honey afforded by the flowers.†dagger

It will now be convenient to describe the general structure of the different forms of flowers produced by each species.

Fuchsia excorticata, L. fil.

In this species the flowers are pendulous, and at first of a deep-purple colour blotched with green; ultimately they assume a dull-red tint. Immediately above the ovary the calyx-tube is dilated in a globular form, then suddenly constricted, when it becomes funnel-shaped; the limb is divided into four acute spreading lobes; the tube is marked externally by eight more or less elevated ridges, caused by the insertion of the filaments; the deep violet-coloured petals are very small, and alternate with the segments of the calyx. The introrse anthers are carried on rigid but very delicate filaments, which vary in length even in the same flower, and are attached to the anthers in an obliquely-peltate manner. The stigma is globose, minutely papillose, and obscurely four-lobed on the upper surface.

Three principal forms of flower may be observed, but each plant produces a single form only. The different forms may be described as under:—

1. The Long-styled Form.—In this form the flower is slightly smaller than either the mid- or short-styled forms. The style is fully twice the length of the calyx-tube, but the filaments are so extremely short that at first sight the anthers appear to be sessile, and in some instances are partially included in the calyx-tube. The pollen-grains when present are yellow, and almost invariably abortive. The petals are very small, and often contorted.

2. The Mid-styled Form.—The style is much shorter than in the previous form, being about one and a half times the

[Footnote] * This character is exhibited by several South American species—probably by all.

[Footnote] † The chief agents in effecting fertilisation in F. excorticata, are the tui (Prosthemadera novœ-zealandiœ), the bell-bird (Anthornis melanura), and, in the extreme north, the stitch-bird (Pogonornis cincta). I suspect that the parrakeets Platycercus novœ-zealandiœ and P. auriceps assist in the process; the white-eye (Zosterops lateralis), and in some cases the naturalised sparrow, although not honey-feeders, certainly render assistance, as the blue pollen-grains are frequently found on their feathers: they doubtless frequent the tree in search of insects, while the tui, the bell-bird, and the stitch-bird are attracted by the honey.

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length of the calyx-tube; the anthers are carried on long filaments, which are shorter than the style and of nearly equal length, although showing a slight tendency to form two sets. The pollen is of a deep mazarine-blue and well developed, the grains differing but slightly from those of the short-styled form. Petals larger than in the long-styled form, never contorted.

3. The Short-styled Form.—In this form the style is shorter than in either of the preceding, while the stamens are longer and of unequal length, the longer alternating with the shorter and nearly equalling the style, or in some cases exceeding it. Petals rather smaller than those of the mid-styled form, but never contorted.

Fuchsia colensoi, Hook. f.

1. The Long-styled Form.—This closely resembles the long-styled-form of F. excorticata, but the filaments are rather longer; the pollen is usually abortive. Petals minute.

2. The Mid-styled Form.—This also corresponds to the mid-styled form of F. excorticata, but the filaments are of equal length and more slender. The pollen is of a deep-blue colour. Petals minute.

I have not seen the short-styled form of this species, but entertain no doubt of its existence. As a rule this species does not produce flowers so freely as F. excorticata, and my opportunities of examining it during the flowering-season have been comparatively few.

Fuchsia procumbens, R. Cunn.

The flowers of this species are invariably erect and apetalous; the calyx-tube is neither inflated at the base nor marked by raised longitudinal ridges, while the segments are always refracted and never spreading. The stamens are exserted and of uniform length.

1. The Long-styled Form.—In this form the style greatly exceeds the stamens, and the stigma is distinctly four-lobed; the anthers are small, and the pollen, although of the same deep-blue colour as the perfect pollen in the preceding species, is probably abortive, but the material at my command is not sufficient to allow this point to be determined. Flowers smaller than in the mid- or short-styled forms. I have not seen this form in a growing condition.

2. The Mid-styled Form.—In this form the style exactly equals the stamens, but the flower differs from the preceding in no other particular, except its larger size.

3. The Short-styled Form.—The style of this form is shorter than the calyx-tube, in which it is wholly included. Pollen bright-blue.

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Flowers of N. Z. Fuchsias

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In F. excorticata the three forms grow intermixed, usually in about the same proportion; although the flowers of each tree are uniform, there is a considerable amount of variation in the flowers on different trees, so that it would not be difficult to find intermediate forms, as in Lythrum grœfferi and L. salicaria.

The long-styled form of F. excorticata is practically a female flower, as the anthers are almost invariably abortive, and it is especially worthy of note that it produces a larger quantity of fruit than either the mid- or short-styled forms. As the three forms are usually found together wherever the plant is plentiful, it may fairly be assumed that this profusion of fruit is largely due to the application of pollen from both the mid- and short-styled forms; but this point can only be determined by an exhaustive series of experiments. The assumption receives a certain amount of support from the fact that, in a few observed cases where the mid-styled form appeared to be absent, the quantity of fruit produced by the long-styled form was greatly reduced. The same result has been observed in the absence of the short-styled form, and it may well be that the paucity or entire absence of fruit on many trees, even after flowers have been produced in profusion, is at least partially due to the absence of one form or the other.

So far as known to me, F. colensoi produces fruit but sparingly, especially in the North Island. May not this be partially due to the absence or comparative rarity of the short-styled form?

No instance is known, so far as I am aware, of the different forms of F. procumbens growing intermixed. I have never seen or heard of more than a single form occurring in any one locality. This may well account for the fact that the handsome fruit of this species has not been seen in the wild state. At Tryphena Bay Professor Hutton and myself examined hundreds of flowers, but saw no trace of fruit; subsequently I had the same experience at Mine Bay, and again at Whangaruru. Its original discoverer saw no trace of fruit at Matauri, where he collected the plant during the autumn months, when fruit should have been plentiful.

Although the mid- and short-styled forms are often cultivated, I have never seen both forms in the same garden. At present the long-styled form has not found its way into cultivation in the colony, although it appears to have been cultivated in England for fifty years, and the short-styled form for twenty years. Cultivated plants of the mid- and short-styled forms grown separately, although most frequently sterile, produce fruits occasionally; sometimes only a single berry becomes mature, rarely more than two or three. On one

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occasion I saw a specimen in a greenhouse bearing nearly a dozen berries, but this was a solitary instance. The seeds are numerous, but possess a low power of germination. Of the total number of seeds contained in two large fruits from a short-styled plant only two germinated; both came true to the parent, and produced short-styled flowers. The rarity of fruit on cultivated plants and its absence on wild plants is surprising when it is remembered that the flowers are erect, and that the anthers and stigma of the mid-and short-styled forms are in such a position that the transfer of pollen by minute insects could scarcely be avoided; moreover, there is no evident tendency to dichogamy.

F. procumbens is an extremely rare and local plant; it is far from abundant in any of the few localities in which it is found. From the absence of fruit in the wild state, in which only a single form of flower is present, and its rare occurrence in cultivation under the same condition, it must be inferred that each form of flower is sterile with its own pollen, or, at least, that it is not capable of fertilisation in any appreciable degree. The same cause doubtless accounts both for the rarity of the plant and its restricted distribution, as well as for its remarkable uniformity in habit and foliage when compared with F. colensoi and F. excorticata.

The following conclusions appear to be warranted by what has been already stated:—

1. Self-fertilisation occurs but rarely, and, so far as evidence is available, the number of perfect seeds produced by self-fertilised flowers is extremely small.

2. The long-styled flowers of F. excorticata and F. colensoi are practically female flowers, but produce fruit more abundantly than either of the hermaphrodite forms.

3. The hermaphrodite forms are reciprocally related, and have a special relationship with the long-styled form.

The precise amount of advantage derived from the fertilisation of the long-styled form of F. excorticata with pollen from both mid- and short-styled forms can only be determined by a long and careful series of experiments. Some advantages must be obtained by the reduced demands upon the vital energy of the plant arising from the non-development of pollen.

As the mid- and short-styled forms of F. procumbens are not unfrequent under cultivation, it would be comparatively easy to ascertain the effects of intercrossing between these forms. The long-styled form is rare, and not easily obtained. It is most desirable that this form should be placed in the hands of the cultivator, since the species is unable to extend itself in a state of nature, and is gradually dying out; while

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its extinction is hastened by the progress of settlement. I have been informed that it has already become extinct in Tryphena Bay.

It is remarkable that the differential characters of F. colensoi and F. procumbens have not been more fully defined: the original drawing of the long-styled form of F. procumbens was published in 1842, and the short-styled form (F.kirkii) in 1871. In the original “Flora Novæ-Zelandiæ,” volume i., page 57, F. colensoi is evidently included under F. procumbens, although the flowers are said to be apetalous; and in the “Handbook of the New Zealand Flora,” page 76, the flowers of F. procumbens are said to be “as in F. excorticata, but smaller.” At page 728 F. colensoi is for the first time described as a distinct species, but very briefly. The Otago botanists have usually mistaken forms of F. colensoi for F. procumbens, although the erect flowers of the latter are alone sufficient to distinguish it from any other species. I venture, therefore, to give the following amended descriptions of the New Zealand species from the MSS. of the “Students’ Flora of New Zealand,” now in course of preparation:—

Fuchsia excorticata, Linné, Supp. 217.

A shrub or small tree 10ft.–45ft. high; trunk 6in.–3ft. in diameter, clothed with brown papery bark. Leaves alternate, ½in.–4in. long, lanceolate or ovate-lanceolate, acute or acuminate, entire or obscurely toothed, membranous, silvery beneath; petioles short. Flowers axillary, solitary, ¾in.–lin. long, trimorphic, on filiform drooping peduncles; calyx globose at the base, then suddenly constricted and expanded into a funnel-shaped tube, with longitudinal ridges, segments 4, acuminate, spreading; petals very small; stamens exserted and, like the style, varying in length. Fruit a pendulous purple or black berry. Link et Otto, Abb., t. 46; Lindl. in Bot. Reg., t. 857; D. C., Prodr., iii., 39; A. Cunn., Precurs., n. 533; Raoul, Enum. Pl. Nov. Zel., 49; Hook. f., Fl. N.Z., i., 56; Handbk. N.Z. Fl., 75; T. Kirk, Forest Fl. N.Z., t. 36 and 36A. Skinnera excorticata, R. and G. Forster, Char. Gen., t. 29; A. Rich., Fl. Nov. Zel., 331. Agapanthus calyciflorus, Banks and Sol., MSS. Kotukutuku, konini (the fruit only).

Hab. On the margins of woods, c., from the North Cape to Stewart Island. Ascends to 3,000ft. Flowers August to December.

In exposed or elevated situations this species is reduced to a dwarf bush. The branchlets are rather stout and very brittle. The petioles and peduncles vary greatly in length.

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F. colensoi, Hook, f., Handbk. N.Z. Flora, 728.

A small erect or prostrate shrub with slender branchlets. Leaves alternate, ovate or orbicular-ovate, rounded or cordate at the base, acute, very membranous when dry, obscurely toothed, rarely silvery beneath; petioles very slender, longer or shorter than the leaves. Flowers as in F. excorticata, but the calyx-tube rather wider at the mouth, and the petals minute.

Hab. Lower Waikato, southward to Stewart Island; more frequent in the South. Ascends to 1,500ft. Flowers October to February.

This species is local in many districts, and always less abundant than the preceding; the flowers are never produced in such profusion. In some places the unbranched flexuous shoots are 8ft. or 9ft. long and subscandent; in others the entire plant scarcely exceeds a foot in height.

F. procumbens, R. Cunn., MSS. in A. Cunn., Precurs., n. 534.

Stems extremely slender, prostrate, 6in.—18in. long. Leaves alternate, rounded - ovate or cordate, obscurely toothed, ¼in.–½in. in length, shorter than the slender petioles. Flowers axillary, solitary, ½in.–¾in. long, on erect peduncles; calyx-tube funnel-shaped, without raised ridges, not dilated at the base; segments oblong, acute, recurved. Petals O. Stamens equal; style varying in length, stigma capitate, four-lobed. Berry large, clavate, glaucous, bright-red. Hook., Ic. Pl., t. 421; Raoul, Enum. Pl. N.Z., 49; Hook. f., Fl. N.Z., i., 57; Handbk. N.Z. Fl., 76. F. kirkii, Hook. f., Ic. Pl., t. 1083.

Hab. North Island. In sandy or rocky places near high-water mark; rare and local. Matauri; Whangaruru; Cape Colville Peninsula; Great Barrier Island. November to February.

This appears to be the only species with erect flowers, and the only apetalous species with the calyx-tube destitute of external longitudinal ridges.

Explanation Of Plate XIX.

Fuchsia excorticata, L. f.

1. Long-styled form. 2. Mid-styled form. 3. Short-styled form.

Fuchsia colensoi, Hook. f.

4. Long-styled form. 5. Mid-styled form.

Fuchsia procumbens, R. Cunnc.

6. Long-styled form. 7. Mid-styled form. 8. Short-styled form.

9. The same in longitudinal section.

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Art. XXXII.—Description of a New Genus and of New Species of Native Plants.

[Read before the Otago Institute, 12th July, 1892.]

Plate XX.

Natural Order Boragineæ

Tetrachondra,* genus novum.

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Flores parvi, tetrameri. Calyx persistens alte 4-fidus, segmentis ovatis obtusis; fructifer immutatus. Corolla subrotata calycem paullo superans, limbi segmentis ovatis, fauce esquamata, æstivatione imbricata. Stamina 4, sinubus corollæ inserta; filamentis brevibus antheræ subæquilongis; antheræ parvæ rotundatæ dorsifixæ, biloculares, inappendiculatæ. Ovarium 4-partitum; stylus inter lobos erectus ovario 2-plo longior; stigma parvum. Nuculœ sæpius 4 erectæ areola parva basilari affixæ, dorso et apice rotundatæ, setulosæ, inferne triangulares, calycem persistentem stylumque subduplo superantes. Semina erecta, albuminosa; embryo teres albumini subæquilongus, cotyledonibus radiculæ æquilongis. Herba depressa, repens, glabra v. subglabra. Folia omnia oppsita, parva, 1/12–1/10 poll. longa, elliptica, obtusa v. obtusiuscula, integra, carnosula, obscure punctata; petioli latiusculi, plani, interdum, parce setuloso-ciliolati, connati. Flores ramulos breves axillares foliiferos terminantes, sœpius solitarii.

Tetrachondra hamiltonii, sp. un. Plate XX., figs. 8–11.

A slender, perennial, matted and creeping herb. Leaves gland-dotted, small, elliptic, obtuse, entire, glabrous, subsessile, in opposite pairs; petioles connate and shortly sheathing the stem.

Flowers axillary, minute, subsessile, solitary, the slender peduncle elongated and decurved in fruit. Other characters as in genus.

Hab. Wet clay hollows in fields at Waipahi; and wet grounds at Hindon and Sutton Creek (Strath Taieri). This remarkable plant clearly belongs to the order Boragineœ; but its position in the order must for the present remain uncertain. Mr. N. E. Brown, A.L.S., and Professor Oliver, of Kew, think

[Footnote] *Through the courtesy of the Secretary to the Institute I have been able to include the generic character, as published by Professor Oliver in the “Icones Plantarum.” An excellent plate (No. 2250, Fourth Series, vol. iii.) accompanies the character.

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it should be placed in the tribe Borageœ, next to Eritrichium, Schrad.; but its abundant albumen separates it sharply from the genera of this tribe, which are all ex-albuminous. I have a very slight acquaintance with this natural order, which is represented in New Zealand only by Myosotis, Linn., Exarrhena, Br., and Myosotidium, Hook., in addition to the genus here described, and I shall therefore offer no opinion as to its position in the order. Mr. Brown informs me that my plant is identical with Tillœa hamiltonii, T. Kirk, noticed in a paper by Mr. W. S. Hamilton in volume xvii., page 292, of the Transactions of the New Zealand Institute, specimens of which Mr. T. Kirk, F.L.S., had sent to the Kew Herbarium. Mr. Kirk's specimens were very imperfect; otherwise I should not have had the opportunity of bringing this interesting new genus under your notice. To avoid useless synonymy I have retained the specific name proposed by Mr. Kirk.

Tillœa novœ-zelandiœ, sp. nov.

A short, slender, matted species, with the stems erect and lin. long, or prostrate and rooting when they reach a length of 2in. or more. Leaves linear, acute, opposite, connate at the base. Flowers axillary, solitary, small, shortly peduncled, 4-merous. Sepals coherent at the base. Petals ovate, acute, longer than the calyx. Stamens alternate with the petals. Scales linear, thin, flat. Style long, reflexed. Seeds, two or three in each carpel.

Hab. Waipahi, Lake Waihola, Lake Te Anau.

The specimens from Waipahi are taken as the type. Those from Lake Waihola are more robust and creeping. The Te Anau ones are very slender, and have fewer, shorter, and narrower leaves. Mr. N. E. Brown, A.L.S., of Kew, informs me that he cannot detect scales in the specimens I forwarded to the Royal Herbarium; but they are constantly present, and can be readily found in the bud and in newly-opened flowers. They are not so easy to detect in older, and especially in dried, flowers, in which they may be readily overlooked or mistaken for parts of the filaments. In some respects the present species resembles Tillœa debilis, Colenso, but the scales and the much longer petals readily distinguish it from that species. It is not so slender or densely matted as Tillœa sinclairii, Hook. f.

Azorella nitens, sp. nov.

A small, creeping, matted, glossy-green plant, the scapes and petioles usually buried in the soil for quite half their length. Leaves broadly-cuneate in outline; usually three-partite to the base, rarely shortly three-lobed; the segments

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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.]

½3/16in. long, ovate-oblong, obtuse, entire, thickened at the margin; petiole slender, 1in. to 2in. long.

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Scapes as long as the leaves, bearing one to three leaf-like petiolate bracts at the middle, where they usually subdivide into two or three branches. Umbels few-flowered (flowers 2 or 3); involucral bracts short, linear, acute; pedicels as long as the fruits or shorter. Fruits turgid, rounded at the back, broader than thick, deeply grooved between the mericarps, ½1/16in. long; ribs absent or very indistinct.

Hab. Shores of Lake Te Anau and banks of Clinton River (700ft.—1,000ft.). The small number of flowers in the umbel, the turgid almost ribless carpels, and the leaves three-partite to the base, mark this species off from all its congeners in New Zealand. In habit it much resembles Hydrocotyle muscosa, Br.

Lagenophora linearis, sp. nov.

A minute plant, with numerous entire, flat, glabrous, narrow-linear leaves, ½¼in. to ½¾in. long.

Scapes very slender, solitary or several, about twice as long as the leaves, elongating in fruit to nearly thrice their length.

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Involucral scales broadly-oblong with dark-purple tips; flowers as long as the involucre. Heads broader than long, minute, ½1/16in. in length; receptacle flat, rather broad. Achenes compressed, linear, tapering at both ends.

Hab. Grassy flats on the shores of Lake Te Anau. A very inconspicuous plant, easily overlooked if not in flower.

Carmichœlia curta, sp. nov.

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A slender, sparingly-branched shrub about 2ft. high; branches dichotomous, subcompressed, grooved and striate, glabrous; leaves not seen. Flower-clusters alternate on the shoots, erect, racemose, 8–10-flowered, with pilose peduncles and pedicels; flowers ½1/6in. long, on pedicels as long as the calyx. Calyx more or less pilose, campanulate, shortly toothed, usually with two small bracts at the base. Corolla rather large, creamy-yellow striped with purple; the the standard longer than the wings, broad, very obtuse. Ovary more or less pilose.

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Ripe pods almost or quite glabrous, when immature generally pilose, ½1/6in. long; beak half the length of the pod, subconical, sharply curved towards the tip; pods thin, two or three-seeded; seeds subreniform, usually pale-green with dark spots and blotches.

Hab. Waitaki River, at Duntroon and Kurow. The present species is most closely allied to C.juncea, Colenso. The flowers are, however, twice as large as in that species, the racemes

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more pilose, the young pods generally pilose, and the pods and seeds nearly twice as large. In C. juncea, Col., the seeds are smaller, rounder, and more elongated. Flowering and fruiting specimens were gathered in the month of March.

Carmichœlia diffusa, sp. nov.

A low, slender, semi-erect, branched shrub.

Branches slender, grooved and striate, narrow, compressed, glabrous.

Racemes short, of 6 or fewer flowers, springing from the axil of a prominent white scale. Flowers ½⅛in. long, on short pilose pedicels. Calyx glabrous, undulate and jagged or ciliate at the margin which is hardly toothed; ovary glabrous; pedicels not longer than the flowers.

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Pods four or fewer in each raceme, ½1/6in. long, ½1/10in. wide, bluntly and broadly obovate, abruptly narrowed into a very short, straight, subulate beak continuous with the upper half of the pod; inner surface of pod puberulous, not cottony; replum strong; sides thick, slightly wrinkled, at length falling away, leaving the seed attached to the replum as in C. australis, Br. Seeds usually solitary, rarely two in a pod, large (½1/11in. long, ½1/15in. broad), subterete, stouter at one end, yellow-brown with dark-green or blackish spots.

Hab. East coast of Otago, near the mouth of the Otepopo River. The pod of this species is very characteristic. It resembles that of C. corymbosa Colenso, and some states of C. flagelliformis, Col., but is shorter, smaller, and broader at the apex. The seeds are much larger than in C. flagelliformis, and are not detached when the sides of the pod fall away.

Ourisia prorepens, sp. nov.

Stems slender, creeping and rooting, more or less branched, 4in. long or less.

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Leaves loosely bifariously imbricate, ½½in. long, ½¼in. to ½1/3in. broad, obovate, crenate, obtusely rounded at the apex, contracted into a broad thin petiole one-third the length of the blade, densely glandular-pilose above, slightly glandular-pilose below, not recurved at the margin; veins distinct on the undersurface.

Scapes slender, 4in. high or less, slightly glandular-pubescent; bracts in pairs, leaf-like, crenate or shortly lobed, nearly glabrous; flowers 3 to 6, solitary, on slender petioles lin. to 1.½in. long. Calyx ½¼in. long, divided to the middle into five oblong, obtuse, glandular-pubescent, and finelyciliate lobes. Corolla large, ½¾in. long and broad, the tube nearly twice as long as the calyx. Style very slender, twice as long as the calyx. Ripe fruit not seen.

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To illustrate paper by D. Petrie

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Hab. Mount Bonpland, 4,000ft. The present species is somewhat closely allied to O. glandulosa, Hook. f., differing in the larger crenate leaves, the longer and more slender scape and peduncles, the larger and longer flowers, the crenate or shortly-lobed bracts, and the slight pubescence of the scape, bracts, and flowers.

Carex novœ-zelandiœ, sp. nov.

A short reddish-brown species, forming small tufts with stiff erect leaves that are curled at the tips. Culms, 4in. high or less, leafy, slender, terete, smooth. Leaves, always as long as, and usually longer than, the culms, very narrow, plano-convex, or concave above and convex below, smooth above, striate on lower surface, stiff, rather obtuse, curled and twisted at the tip.

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

Spikelets 4 or 5, ½1/5in. long, rather stout, erect, the lowermost usually distant, the others crowded, sessile or shortly-peduncled; uppermost spikelet male only, the rest female with a few male flowers at the base; bracts as long as the leaves, leaf-like.

Glumes membranous, broadly-ovate, entire, rather obtuse, nerved and apiculate.

Utricle biconvex, smooth or faintly ribbed, gradually and equally narrowed at either end, red-brown; beak smooth, hardly bifid.

Style-branches, two.

Hab. Boggy ground at the edge of Lake Te Anau. Gathered February, 1892.

This plant has much the same appearance as Carex petriei, Cheeseman; the twisted and curled tips of the leaves readily mark it off from all the other native species. From C. petriei it differs in having two style-branches, much shorter spikelets, narrower and more rigid leaves, and less turgid utricles.

Gastrodia minor, sp. nov. Plate XX., figs. 5—7.

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

A much smaller and more slender plant than Gastrodia cunninghamii, Hooker fil. Stems 8in. to 15in. high, terete, polished, ½1/12in. to ½1/16in. in diameter near the base; scales few, forming short oblique subacute sheaths round the stem, the upper ones distant; the whole plant except the tips of the flowers of a uniform umber-brown colour, not spotted.

Racemes lin. to 3in. long, of 1 to 9 pendulous flowers (usually 3 to 5). Bracts short, rather broad, scarious. Pedicels slender, 2 lines long; ovary as long as the pedicel, ribbed, slightly tuberculate. Perianth 5 lines long, ventricose, 5-fid, the very narrow division behind the labellum extending to about one-third the length of the tube, the others

– 274 –

very shallow (less than 1 line deep); the sepals and two inferior petals rounded, undulate, crumpled and incurved along the thickened margin; tips and inner surface of the perianth-lobes dirty-white.

Labellum, included, oblong, dull-yellow, sometimes slightly expanded at the base, with two subpapillose narrow more or less confluent medial ridges, incurved and thickened at the undulating and crumpled margin; the upper third free, the lower half adnate to the tube and with or without obscure ridge-like wings at the sides.

Column short, with straight very short lateral appendages that are either acute or obtuse.

Hab. Town Belt, Dunedin, in shady manuka bush. Flowers first weeks of January.

The present species differs from G. cunninghamii, H. f., in its small size, short racemes, smaller flowers, and umber-brown colour, but most of all in the structure and attachment of the labellum. Mr. A. Hamilton has kindly drawn for me the flowers of both species, and his drawings show the points of difference plainly enough. In G. cunninghamii (Plate XX., figs. 1—4) the free part of the labellum is trowel-shaped and much thinner at the sides than in my plant, and it has a distinct claw which is wanting in G. minor. The curiously-twisted wing of the lower part of the labellum of the former is wholly absent in the present species, in which, moreover, all the divisions of the flower except the labellum are of equal length. The lateral appendages of the column in G. cunninghamii are slender, curved, and horn-like; in G. minor they are short, erect, and straight. I had the good fortune to find both plants in flower in the neighbourhood of Dunedin at the same time, so that a very complete comparison of the two species was practicable. The flowers of the present species open but very slightly, and the groove behind the labellum cannot be seen without pushing apart the sepals which the latter separates.

Gunnera ovata, sp. nov.

Rhizome creeping, tufted.

Leaves broadly-ovate, obtusely rounded at the tip and cordate or subcordate at the base, finely crenately toothed all round the margin, nearly glabrous or with short scattered pale hairs, about lin. long and ½¾in. broad. Petiole slender, glabrous or more or less clothed with short pale hairs, twice as long as the blade.

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

Flowers on peduncles about ½in. long, lengthening in fruit to 1.½in. Male flowers in a slender interrupted spike 2in. to 3in. long; female flowers forming a dense oblong spike about 1/3in. long; Fruiting spike ¾in. long, rather slender; drupes

– 275 –

⅛in. long, sessile, turbinate, dark-red, placed at right angles to the peduncle, not pendulous.

Hab. South Island—Lake Te Anau; Catlin's River; mouth of the Clutha; Hindon; and Kaikorai (Dunedin). North Island—Near Erehwon (Upper Rangitikei). I hear from Mr. N. E. Brown, of Kew, that this species is the plant, gathered near the base of Tongariro by Colenso, and in the South Island by Dr. Lyall, to which Sir Joseph Hooker refers at page 68 of the Handbook as a probable fourth species of Gunnera. It grows only in ground saturated for most of the year with water, and is generally accompanied by masses of Sphagnum.

Agrostis multicaulis, Hook. f.

This species was gathered by me in January of the present year at the head of the Clinton Valley (Te Anau). It is a native of Campbell Island, and has now been met with for the first time on the mainland of New Zealand. I am not sure that there are sufficient grounds for merging this species in A. antarctica, Hook. f., as Sir Joseph Hooker has done in the “Handbook of the New Zealand Flora.” At any rate, the plant from the Clinton Valley differs widely from that figured as A. antarctica, Hook. f., in vol. ii. of the “Flora Antarctica.”

Explanation of Plate XX.

1.

Flower of Gastrodia cunninghamii, Hook. fil.

2.

Column and labellum of ditto.

3.

Column and appendages of ditto (enlarged).

4.

Perianth of ditto laid open.

5.

Part of spike of Gastrodia minor.

6.

Column of ditto.

7.

Perianth of ditto laid open.

8.

Flowering branch of Tetrachondra hamiltonii (enlarged).

9.

Corolla of ditto laid open.

10.

Flower of ditto, the corolla and front lobes of the calyx removed.

11.

Fruit of ditto.

– 276 –

Art. XXXIII.—Notes on the New Zealand Species of the Genus Andreæa, together with Descriptions of some New Species.

[Read before the Philosophical Institute of Canterbury, 2nd November, 1892.]

Plates XXI.-XXXI. (in Part).

The following account of the genus Andreœa as it occurs in New Zealand is a portion of the results of ten years’ work, studying and collecting the Musci of New Zealand in their native habitats, and figuring the various species and varieties with the camera lucida. All the plants described have been collected by myself, many of them in localities previously unbotanized, notably the Clinton Pass, Sutherland Falls, South Fjord of Lake Te Anau, in Otago; Moa Creek, Walker's Pass, the Craigieburn and Puketeraki Mountains, in Canterbury; and the western slopes of the Southern Alps in Westland; together with Mount Thompson and the Ruggedy Mountains in Stewart Island. I am with reluctance approaching this subject prematurely, much remaining yet to do, but from circumstances which have recently transpired I am forced to do so in order to protect my own rights; for, acting on the suggestion of the late Sir Julius von Haast, I presented nearly all my specimens and camera-lucida drawings to the Christchurch Museum, where they remain for any one to describe who may think fit to rob me of my hard-earned rights.

The genus Andreœa in New Zealand, as in other countries, comprises species of an alpine or subalpine character, only growing under an elevation of 2,000ft. when exposed to a constant stream of moist air in exceptionally cold localities. They are found in rocky situations, often growing under great difficulties, their roots fixed in rocky depressions, which after rain retain a few drops of moisture, exposed at the same time to the full heat of the sun, and to periods of drought which would utterly destroy them were they not possessed of the power to extract moisture from the air. I have often, when collecting these plants in dry weather, had to moisten them with saliva, whereupon the apparently dead plant, owing to its hygrometric leaves, would revive. With regard to the leaves, those found about the middle of the stem have in many of the species much resemblance to each other, varying principally in breadth and obliqueness. This is very perplexing, so I have adopted the plan of figuring all the leaves from base to apex of the plant, including the perichætial,

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these latter being of the greatest importance in the determination of species. following this plan, a graduated series is found in the shape of the leaves, beginning with those at the base and running up to the perichætial. Thus, I do not think there should be any difficulty in recognising the new species here described.

All the Andreæas described in the Handbook are figured in the “Flora Antarctica” except Andreœa petrophila, and are there available for reference. To complete the series, I have added drawings of A. petrophila, taken from a Swedish specimen (Pl. XXXI.). The perichætial leaves are large in all the New Zealand species except A. subulata, in which they are described in the Handbook as small and inconspicuous. This plant I have never seen. These leaves play an important part in protecting the young capsule from being destroyed by great extremes of temperature. In three of the species the vaginula has been found sessile and the spores appeared to have matured, while on the same plants were found the remains of the previous year's capsule with a stalked vaginula, showing that this stalk had been subsequently developed. With regard to distribution, some of the species are very common, while others are extremely local, A. aquaticus and A. aquatilis having been found in one locality only.

The following arrangement of the species of this genus in its enlarged state is that adopted by Sir J. D. Hooker in the Handbook, and is intended to place the plants in the position they relatively hold. In the present condition of the genus it is perhaps the best, as it is not known how many of the species are diœcious:—

Nerveless.

  • acutifolia, Hook. and Wils.

  • gibbosa, sp. nov.

  • petrophila, Ehrk.

  • dioica, sp. nov.

  • minuta, sp. nov..

  • novæ-zelandiæ,sp. nov.

  • wrightii, sp. nov.

  • mutabilis, Hook, f.

  • flexuosa, sp. nov.

  • huttoni, sp. nov.

  • nitida, Hook. and Wils.

  • aquatica, sp. nov.

Nerved.

  • subulata, Harv.

  • dicranioides, sp. nov.

  • ovalifolia, sp. nov.

– 278 –
  • apiculata, sp. nov.

  • cockaynei, sp. nov.

  • jonesii, sp. nov.

  • clintoniensis, sp. nov.

  • lanceolata, sp. nov.

  • aquatilis, sp. nov.

Andreæa gibbosa, sp. nov. Plate XXI.

Plants small, densely tufted, about ¼in. high, fastigiately branched. Leaves dark reddish-brown, small, densely imbricating, erecto-patent, slightly incurved towards the tips, subulate-lanceolate, acute, concave, sheathing and gibbous at the base, margins entire, nerveless; perichætial large, erect, not gibbous at base, inner pair elliptic-lanceolate, acute, convolute, sheathing, outer pair lanceolate, acute, nerveless, minutely papillose.

Hab. Moa Creek, on rocks; June, 1885. Port Hills; 1883.

Andreæa dioica, sp. nov. Plate XXI.

Plants very small and densely tufted. Stem from ⅛in. to ½in. long, fastigiately branched. Leaves brownish-green, lower extremely small, deltoid, acute, becoming larger immediately below the perichætial leaves, then ovate-subulate, acute, very concave, margins entire, nerveless, minutely papillose on the back, appressed when dry; perichætial large, erect, ovate-lanceolate, obtuse, slightly cucullate, semi-convolute, margins incurved. Capsule subrotund, apiculate. Diœcious.

Hab. On rocks, Moa Creek; June, 1885.

Andreæa minuta, sp. nov. Plate XXI.

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

Plants very small, densely tufted. Stem 1/16in. long or more, fastigiately branched. Leaves brown, erecto-patent, imbricating, ovate-subulate, acute, oblique, margins entire or minutely papillose near the apex, nerveless, concave, papillose on the back, appressed when dry; perichætial larger, erect, outer pair larger than the inner, semi-convolute, broadly oblong-lanceolate, acute, inner pair ovate-lanceolate, acute, nerveless, papillose.

Hab. On rocks, Moa Creek; June, 1885.

Andreæa novæ-zelandiæ, sp. nov. Plate XXII.

Plants small, densely tufted. Stem from ¼in. to ½in. long, fastigiately branched. Leaves dark red-brown, erecto-patent, slightly incurved, lower subulate-lanceolate, acute, upper narrow ovate-lanceolate, acuminate, concave, margins entire, nerveless, appressed when dry; perichætial large, erect, broadly-ovate or oblong-acuminate, slightly incurved near the apex, outer pair convolute, inner pair narrower, concave.

Hab. On rocks, Moa Creek; 1885.

– 279 –

Andreæa wrightii, sp. nov. Plate XXII.

Plants small, densely tufted, ¼in. long, nearly naked below, fastigiately branched. Leaves closely imbricating, erecto-patent, lower scale-like, middle small, varying from subulate-lanceolate to narrow ovate-lanceolate, acute, upper larger, concave, nerveless, papillose, margins entire; perichætial large, erect, semi-convolute, outer and inner pair sheathing two-thirds of their length, oblong-lanceolate and narrowed into an obtuse cucullate apex, nerveless, appressed when dry. Capsule ovate-apiculate.

Hab. Rocks, Moa Creek; June, 1885. Dedicated to Mr. Thomas G. Wright, of Christchurch, an earnest cryptogamic botanist.

Andreæa mutabilis, Hook. f. and Wils. (Enlarged and revised description.) Plate XXII.

Plants densely tufted. Stem ¼in. to 1in. high, branched. Leaves dark red-brown, erecto-patent, lower deltoid-subulate, acute, middle ovate-lanceolate, tapering into an acute point, upper ovate-subulate, acute, concave, margins entire, nerveless, papillose on the back, often falcate, appressed when dry; perichætial larger, erect, sheathing, convolute, ovate-lanceolate, acuminate, nerveless, incurving near the apex.

Var. β. All the upper-stem leaves hamulose.

Hob. Port Hills; Craigieburn Range, Arthur's Pass, Moa Creek. Var. β. Clinton Valley, Otago.

Andreæa flexuosa, sp. nov. Plate XXIII.

Plants densely tufted. Stem from ¼in. to ¾in. long, fastigiately branched. Branches short. Leaves erecto-patent, imbricating, dark-brown, flexuous, sheathing near the base, linear-lanceolate, acute, concave, margins entire, nerveless, appressed when dry; perichætial erect, sheathing, convolute, obliquely ovate-subulate, obtuse, slightly cucullate at the apex, nerveless.

Hab. Arthur's Pass, on rocks; June, 1884. Moa Creek; June, 1885.

Andreæa huttoni, sp. nov. Plate XXIII.

Plants growing in small loose tufts. Stems from ¼in. to ½in. long, branched. Leaves red-brown, closely imbricating, erecto-patent, lower small, ovate - subulate, obtuse, oblique, middle ovate-lanceolate, obtuse, oblique margin incurved above the middle, cucullate at the apex, upper larger, nerveless, margins entire, concave; perichætial erect, large, sheathing nearly three-fourths of their length, convolute, narrowed into an obtuse cucullate apex, nerveless, closely appressed when dry. Capsule small.

– 280 –

Hob. Rocks, Moa Creek; 1885. Named in honour of Professor Hutton, of Christchurch.

Andreæa aquatica, sp. nov. Plates XXIII. and XXIV.

Plants growing in large loose tufts from 1in. to 4in. long. Branches flexuous, long. Leaves large, spreading, very crisp, brownish - green, glossy, middle broadly-ovate or subrotund, upper broadly ovate-acuminate, concave, margins entire, nerveless, scarcely altered when dry; perichætial very large, erect, outer lanceolate, acuminate, concave, inner sheathing, convolute, oblong-lanceolate, acuminate, incurved from the middle, nerveless. Capsule very large.

Hab. Growing submerged in water on stones in a small stream on Kelly's Hill, Westland, at an altitude of 3,500ft.; November, 1889.

The most beautiful of all the New Zealand Andreæas, being finely crisped, and of a shining brown and green colour.

Andreæa dicranioides, sp. nov. Plate XXV.

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

Plants growing in dense tufts, fastigiate, 1/3in. to ¾in. long. Leaves red-brown, imbricating, secund, strongly falcate, base concave, narrowly-ovate or linear, tapering rapidly into a long slender point four-fifths of the length of the leaves, nerve slender, sometimes nearly absent. Specimen not in fruit.

Hab. Rocks on side of small tarn below Lake Mintaro, Clinton Valley; 1889.

Andreæa ovalifolia. sp. nov. Plate XXV.

Plants growing in dense tufts from ¼in. to 2in. long. Stems slightly fastigiately branched. Leaves spreading, large, darkbrown, scale-like at the base, middle oval, upper oval, shortly acute or broadly ovate-acute, concave, nerve broad ending about middle, margins entire, appressed when dry; perichætial large, erect, broadly-ovate, ending in a small point, margins entire, nerveless.

Hab. Port Hills, on rocks; October, 1883. Mount Torlesse; January, 1886. Waimakariri glaciers; 1890. Mount Bosquet; 1888.

Andreæa apiculata, sp. nov. Plate XXVI.

Plant loosely tufted, from 1in. to 1.½in. long, slightly branched. Branches slender, fastigiate. Leaves erectopatent, brownish-green, shining, lower scale-like, middle ovateoblong or obovate, rounded into a short acute point, concave, nerve disappearing near the middle, margins entire, upper very large, broadly-lanceolate, acute, nerve disappearing at the middle, margins entire, very concave, appressed when dry;

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Andreœa. gibbosa sp.nov.

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Andreœa. novœ. Zealandiœ sp.nov.

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Andreœa flexuosa sp.nov.

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Andreœa aquatica sp.nov.

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Andreœa dicranioides sp.nov.

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Andreœa apiculata sp.nov.

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Andreœa Cockaynei sp.nov.

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Andreœa Jonesii sp.nov.

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Andreœa Jonesii sp.nov.+

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Andreœa lanceolata sp.nov

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Andreœa petrophila Ehrhart

– 281 –

perichætial erect, large, sheathing, convolute, cucullate at apex. Capsule large.

Hab. Precipitous rocks forming one side of a small tarn below Lake Mintaro, Clinton Valley; January, 1890.

Andreæa cockaynei, sp. nov. Plate XXVII.

Plants growing in dense tufts. From ½in. to 1in. long, fastigiately branched. Leaves erecto-patent, densely imbricating, yellow-brown at the tips of the branches, dark-brown below, lower minute, ovate-subulate or ovate-cordate, falcate, nerved to the apex, concave, margin entire, middle and upper leaves oblong-lanceolate, tapering rapidly into a long slender point, slightly falcate, concave, nerveless. Immediately outside the perichætial are a few large leaves, oblong-ovate, rounded into a short or long point, concave, nerveless, appressed when dry; perichætial leaves erect, sheathing, oblong or elliptic-lanceolate, acuminate, convolute, nerveless. Capsule small.

Hab. Rocks side of small tarn below Lake Mintaro, Clinton Valley, Otago. Named in honour of Mr. L. Cockayne, my botanical companion in many rough journeys among the mountains.

Andreæa jonesii, sp. nov. Plates XXVIII. and XXIX.

Plants densely tufted, from ¼in. to ½in. long. Stems flexuous, simple or slightly branched, fastigiate. Leaves erecto-patent, red-brown, closely imbricating, middle ovatelanceolate, rapidly tapering into a long slender point for about two-thirds the length of the leaf, upper large, broadly oblonglanceolate, rapidly tapering into a long point for one-third the length of the leaf, straight or slightly falcate, margin entire, concave, nerved; perichætial, inner pair elliptic-lanceolate, gradually tapering into a slender point, convolute, sheathing, outer larger, oblong-lanceolate, rapidly constricted into a slender point, convolute. Diœcious, leaves of male plant strongly falcate.

Hob. On rocks, Moa Creek; June, 1885.

Var. β. Upper leaves shorter in the blade and the point longer in proportion; perichætial larger and the capsule smaller than in the type.

Hab. Rocks on Mount Torlesse; January, 1886. Rocks above Robinson's Bay, Banks Peninsula. Named after the late F. Jones, Esq., M.H.R.

Andreæa clintoniensis, sp. nov. Plate XXIX.

Plant densely tufted, from ½in. to lin. long. Stems simple or sparingly branched, fastigiate. Leaves yellow-brown near apex of branch, dark-brown below, erecto-patent, slightly incurved, lower linear-lanceolate, acute, upper ovate or oblong-

– 282 –

lanceolate, acute, margins recurved, nerved to apex, appressed when dry; perichætial about same length as upper leaves, semiconvolute, ovate-lanceolate, acuminate, nerved to apex. Capsule ovate.

Hab. Rocks on side of tarn below Lake Mintaro, Clinton Valley, Otago; 1889.

Andreæa lanceolata, sp. nov. Plate XXX.

Plants growing in dense tufts about 1in. high. Stems simple or fastigiately branched. Leaves brownish-green, large, spreading, appressed when dry, incurved towards the apex, loosely imbricating, oblong-lanceolate, acute, nerved to the apex, margin recurved, concave, smaller towards base; perichætial large, erect, concave, inner smaller, apex of leaves inflexed over the capsule. Capsule ovate.

Hab. Moa Creek, on rocks; June, 1885.

Andreæa aquatilis, sp. nov. Plate XXX.

Plants large, loosely tufted, from 2in. to 5in. long. Stem flexuous, sparingly branched. Leaves very dark - brown, spreading, incurved from the middle towards the apex, lower small, lanceolate, acute, upper shortly ovate-lanceolate, acute, concave, margin entire, nerved to the apex, loosely appressed, shrivelled when dry; perichætial large, erect, outer broadly lanceolate-acuminate, concave, nerved to the apex, inner smaller. Capsule very large, broadly ovate.

Hab. On stones in a small tarn, submerged in the water, towards summit of Kelly's Hill, Westland.

Description of Plates XXI.–XXXI. (in Part).

Plate XXI.

Andreœa gibbosa, sp. nov.
  • Figs.

  • 1, 2. Lower stem leaves.

  • 3, 4, 5. Middle and upper stem leaves.

  • 6. Tip of a branch.

  • 7, 8. Outer pair of perichætial leaves.

  • 9, 10. Inner pair of perichætial leaves.

Andreœa dioica, sp. nov.
  • 1, 2. Lower stem leaves.

  • 3, 4. Middle stem leaves.

  • 5. Upper stem leaf.

  • 6. Outer perichætial leaf.

  • 7. Inner perichætial leaf and capsule.

Andreœa, minuta, sp. nov.
  • 1, 2. Lower stem leaves.

  • 3, 4. Middle and upper stem leaves.

  • 5, 6. Outer pair of perichætial leaves.

  • 7, 8. Inner pair of perichætial leaves.

– 283 –

Plate XXII.

  • Figs. Andreœa novœ-zelandiœ, sp. nov.

  • 1, 2. Lower stem leaves.

  • 3, 4. Middle and upper stem leaves.

  • 5, 6. Outer pair of perichætial leaves.

  • 7, 8. Inner pair of perichætial leaves.

Andreœa wrightii, sp. nov.

  • 1, 2, 3. Lower stem leaves.

  • 4, 5, 6. Middle and upper stem leaves.

  • 7. Outer pair of perichætial leaves.

  • 8, 9. Inner pair of perichætial leaves and capsule.

Andreœa mutabilis, Hook. f.

  • 1, 2. Lower stem leaves.

  • 3. Middle stem leaf.

  • 5. Upper stem leaf.

  • 4, 6. Outer pair of perichætial leaves.

  • 7, 8. Inner pair of perichætial leaves.

Plate XXIII.

  • Figs. Andreœa flexuosa, sp. nov.

  • 1, 2, 3, 4. Middle stem leaves.

  • 5. Upper stem leaf.

  • 6. Outer perichætial leaf.

  • 7. Inner perichætial leaf and capsule.

Andreœa huttoni, sp. nov.

  • 1. Lower stem leaf.

  • 2. Middle stem leaf.

  • 3. Upper stem leaf.

  • 4. Outer perichætial leaf.

  • 5. Inner perichætial leaf.

  • 6. Capsule.

Andreœa aquatica, sp. nov.

  • 1. Lower stem leaf.

  • 2. Middle stem leaf.

  • 3. Upper stem leaf.

Plate XXIV.

  • Figs. Andreœa aquatica, sp. nov.

  • 1. Outer perichætial leaf.

  • 2. Inner perichætial leaf.

  • 3. Capsule.

Plate XXV.

  • Figs. Andreœa dicranioides, sp. nov.

  • 1, 2. Lower stem leaves.

  • 3, 4, 5. Middle stem leaves.

  • 6. Upper stem leaf.

  • 7. Tip of a branch.

Andreœa ovalifolia, sp. nov.

  • 1, 2. Lower stem leaves.

  • 3, 4. Middle and upper stem leaves.

  • 5. Outer perichætial leaves.

  • 6. Inner perichætial leaves.

– 284 –

Plate XXVI.

  • Figs. Andreœa apiculata, sp. nov.

  • 1, 2. Middle stem leaves.

  • 3. Upper stem leaf.

  • 4. Outer perichætial leaf.

  • 5. Inner perichætial leaf and capsule.

Plate XXVII.

  • Figs. Andreœa cockaynei, sp. nov.

  • 1, 2. Lower stem leaves.

  • 3, 4. Middle stem leaves.

  • 5, 6. Upper stem leaves.

  • 7, 8. Leaves immediately outside the perichætial.

  • 9. One of outer pair of perichætial leaves.

  • 10. Inner pair of perichætial leaves and capsule.

Plate XXVIII.

  • Figs. Andreœa jonesii, sp. nov.

  • 1, 2. Middle stem leaves.

  • 3. Upper stem leaf.

  • 4, 5. Outer pair of perichætial leaves.

  • 6, 7. Inner pair of perichætial leaves.

  • 8. Capsule.

Plate XXIX.

  • Figs. Andreœa jonesii, sp. nov., var. β.

  • 1, 2. Middle stem leaves.

  • 3. Upper stem leaves.

  • 4. Inner perichætial leaf.

  • 5. Outer perichætial leaf.

  • 6. Capsule.

Andreœa clintoniensis, sp. nov.

  • 1, 2. Middle stem leaves.

  • 3. Upper stem leaf.

  • 4. Outer perichætial leaf.

  • 5. Inner perichætial leaf and capsule.

Plate XXX.

  • Figs. Andreœa lanceolata, sp. nov.

  • 1. Lower stem leaf.

  • 2, 3. Middle stem leaves.

  • 4. Upper stem leaf.

  • 6. Outer perichætial leaf.

  • 5. Inner perichætial leaf.

  • 7. Capsule.

Andreœa aquatilis, sp. nov.

  • 1, 2. Lower stem leaves.

  • 3. Upper stem leaf.

  • 4. Middle stem leaf.

  • 5. Outer perichætial leaf.

  • 6. Inner perichætial leaf.

  • 7. Capsule.

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Kennedia in termedia sp.nov.

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Hennedia microphylla sp.nov.

– 285 –
Plate XXXI. (in Part).
  • Figs. Andreœa petrophila, Ehrhart.

  • 1, 2. Middle stem leaves.

  • 3, 4. Upper stem leaves.

  • 5. Inner perichætial leaf.

Art. XXXIV.—Notes on a Proposed New Genus of New Zealand Mosses; together with a Description of Three New Species.

[Read before the Philosophical Institute of Canterbury, 7th September, 1892.]

Plates XXXI. (in Part) to XXXIII.

During the year 1882, having been engaged in botanizing on the Port Hills, from the lighthouse at the Heads to Cooper's Nob at the opposite end of the harbour, and on the plains round Christchurch as far as the banks of the River Waimakariri, amongst a number of new mosses then discovered by me were three which could not be placed in any of the existing genera, they, however, being most nearly related to Encalypta, yet differing from that genus in their having a short, stout, straight beak, instead of a long, slender, straight beak, while the calyptra, instead of being inflated as in that genus, closely encloses the capsule, and is confluent at the base. Since these two generic characters are the very opposite to those of Encalypta, these plants cannot be very well placed in that genus without seriously disturbing the accepted generic characters; consequently it becomes necessary that a new genus should be created to receive these mosses. Acting on the advice of a friend, I took no steps in this matter at the time for creating a new genus, fearing that the above-mentioned mosses might prove to be examples of some foreign genus not represented in the New Zealand flora; however, since this has proved to be not the case, I have brought this subject before the Institute to-night, and propose to name the new genus after the late Rodger Hennedy, Professor of Botany at the Andersonian University, Glasgow, my late admirable teacher and esteemed friend.

Hennedia, Gen. Nov.

Annual or perennial plants. Capsule erect or inclined, ovate or ovate-oblong, symmetrical, narrowed towards the mouth. Operculum short, stout, conic, straight. Calyptra

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mitriform, large, covering the whole capsule, confluent at the base, commonly ruptured at the middle by the lateral growth of the capsule, when maturing very persistent. Peristome none.

Hennedia macrophylla, sp. nov. Plate XXXI.

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

A densely-tufted pale-green perennial moss, about ½in. high. Stem short, fastigiately branched. Leaves nearly erect, oblong-lanceolate, apiculate, slightly narrowed in the middle, concave, slightly recurved near the apex, margined with a subpellucid border of long quadrate cells, serrated towards the apex, from 3/16in. to ¼in. long, upper leaves longest, crisp when dry. Nerve keeled, excurrent. Areola, upper half dense, round; lower half quadrate, pellucid. Perichætial leaves similar to the other leaves. Capsule immersed, hidden by the upper leaves, broadly-ovate, narrowed into the mouth. Operculum short, conic, straight. Calyptra mitriform, large, tightly covering the whole capsule, confluent at the base, and very persistent.

Hab. Banks of the River Avon, near Christchurch. Fruiting from August to November.

Hennedia intermedia, sp. nov. Plate XXXII.

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

Plants growing in small patches, dark-green, about ¼in. high. Stem short, 1/16in. or less, branched near the base. Leaves spreading, lower ovate-lanceolate, apiculate; upper larger, oblong-lanceolate, acute or acuminate, apiculate, serrated towards the apex, as long as or longer than the fruitstalk. Margin with a narrow border of pellucid quadrate cells, nerve percurrent. Areolæ—at the base, large quadrate, membranous; upper roundish. Perichætial leaves longer, otherwise similar. Fruitstalk ⅛in., inclined, thickened upwards. Capsule exserted, ovate-oblong, narrowed into the mouth. Operculum short, straight, conic. Calyptra mitriform, large, closely enclosing the capsule and confluent at the base, very persistent.

Hab. Damp banks, Port Hills, and plantations round the River Avon.

Hennedia microphylla, sp. nov. Plate XXXIII.

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

A small, annual, pale-green moss, whole plant from 2/16in. to 5/16in. high. Simple or branched near the base. Leaves spreading, concave, oblong-lanceolate, acuminate. Margin entire or slightly toothed near the apex. Nerve vanishing or excurrent. Margin with a narrow border of quadrate cells. Perichætial leaves similar to stem-leaves, but slightly longer. Fruitstalk longer than the leaves, thickened upwards. Capsule inclined, ovate-oblong, narrowing towards the mouth. Operculum

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conic, straight, short. Calyptra mitriform, closely enclosing the capsule and confluent at the base, very persistent.

Hab. Damp banks in the neighbourhood of Christchurch. Common; fruiting from September to December.

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

With regard to the determination of these three species, H. macrophylla is quite distinct; but the similarity between H. intermedia and H. microphylla is so marked that I was very reluctant to make the latter anything but a variety of the former. But, after observing these plants for several years in their habitats, I have never found them growing intermingled, nor observed intermediate forms. H. microphylla, moreover, is extremely common, and variable in size, ranging as it does from a plant 1/16in. to 5/16in. in length; yet, however small the plant, it retains all the appearance of the larger ones. The fruitstalk, too, is always longer than the leaves. I may point out that Hennedia is in much the same position with regard to the leaves of its species as that occupied by Dicranum and Campylopus, in which the leaves of many species are almost identical. In conclusion, I may state that I have presented specimens of these species to the Christchurch Museum, so that any one interested in the matter can examine them.

Description of Plates XXXI. (in Past) to XXXIII.

Plate XXXI. (in Part).

Hennedia macrophylla, sp. nov.

Plate XXXII.

Hennedia intermedia, sp. nov.

Plate XXXIII.

Hennedia microphylla, sp. nov.

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Art. XXXV.—Note on Splachnidium rugosum, Grev.

[Read before the Philosophical Institute of Canterbury, 2nd November, 1892.]

This interesting plant is a brown seaweed common on the coasts of both Islands, and growing a foot or two above lowwater mark. It seems to be an annual, as specimens of it are very scarce during the winter months. It occurs at the Cape of Good Hope, and on the Australian coast, as well as in New Zealand. It was first described by Linnæus as Ulva rugosa; but the genus Splachnidium was afterwards founded for its reception by Greville, and it still remains the only species of the genus.

It has hitherto been included in the order Fucaceœ, because of its general external resemblance to them, and because it has conceptacles which were supposed to contain oogonia (v. “Phycologica Australica,” plate xiv., Harvey). However, in May, 1890, I was examining some specimens of this plant which were lying in a saucer exposed to direct sunlight, when I noticed a number of what I took to be oospheres entangled amongst the hairs of a conceptacle near the top of the stem. I mounted them on a slide with sea-water, and burst them by a slight pressure. A large number of zoospores filled with colouring-matter were at once extruded, showing that the bodies in question were sporangia, and that previous observers had been wrong in imagining them to be oospheres. The zoospores were actively swimming in the water, and cilia were distinctly visible on many. Most were egg-shaped, a few were approximately circular, and an eye-spot was frequently discernible. On another slide I obtained some which had come to rest and thrown off their cilia—whether after conjugation or not I cannot say.

Since making these observations I have received a paper entitled, “On Splachnidium rugosum, the Type of a New Order of Algæ,”* by Margaret O. Mitchell and Frances G. Whitting, both of Newnham College. This contains an exhaustive description of the minute structure of the thallus and of the mode of growth; but the special feature of the paper is that the authors have arrived by indirect evidence at the conclusion that the bodies hitherto regarded as oogonia must be sporangia. Their examination of the plant shows that in its vegetative structure it is allied to some extent with the Fucaceœ (e.g., in the possession of a conceptacle), but that on the other hand

[Footnote] * Dulau and Co., Soho Square, London; 1892.

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in its reproduction it is connected with the Laminariaceœ. The sum of its characters, however, is such as to expressly exclude it from any existing natural order. They therefore propose to establish the order Splachnidiaceœ for its reception.

It must be very satisfactory to the authors of this excellent paper to find that the conclusion they have arrived at by theoretical considerations as to the reproduction of this plant is shown by observation to be justifiable and accurate. My own investigations, as far as they go, are quite in accord with theirs as to the minute structure of the thallus. Unfortunately, however, I have not been able as yet to examine the apical cell.

It may be worth mentioning that I have invariably found a particular diatom in the mucilage of this plant. It is spindleshaped, and has a long elastic acicular process at each end. These processes are sometimes straight, sometimes curved or even hooked, and slightly clubbed. This diatom has been found in Splachnidium obtained near Wellington, and also in plants taken from Lyttelton Harbour. It may occasionally be found in the scrapings taken from the surface of the thallus. Those so obtained are more highly coloured with a characteristic brown pigment than those found in the interior, and appear (in some cases, at any rate) to escape through the ostiole. They may often be seen in slow motion, and are certainly worthy of further investigation.

Art. XXXVI.—Description of New Species of Musci.

[Read before the Philosophical Institute of Canterbury, 5th October, 1892.]

Plates XXXIV.–XLIV.

Early in the present year I sent a small collection of New Zealand mosses to Dr. Karl Müller, of Halle. He has very kindly examined them for me, and in a letter I lately received from him, giving me the results of his examination, he tells me that, of the seventy species sent, forty-eight are new. Some of these, I think, will prove to be but varieties of species already described. As Dr. Müller is unable to devote the time necessary to work out the new species, he has suggested that I should describe them, and publish them in the Transactions of the New Zealand Institute. He writes, “Should’ you make known in New Zealand the results of your collecting, and the mosses named by me, and should you feel disposed

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to describe the new species, I very cordially agree with such a course.” The names are those given by Dr. Karl Müller, but for any errors or inaccuracies in the descriptions I am alone responsible. In this paper I have described and figured a few of the most interesting of the new species, and I hope in a future paper to publish some more.

Blindia chrysea, sp. nov. Plate XXXIV.

Autoicous. Densely cæspitose in large tufts, erect, branched, golden-yellow above, dull olive-green below. Leaves densely imbricated, falcate, glossy, when dry the apices spirally twisted, oblong-lanceolate produced into a long narrow point, margin flat, quite entire; nerve green, thin, well defined, occupying the greater part of the subulate apex. Alar cells dark rufous-brown, large and inflated, cells of lower part of leaf long, narrow, becoming shorter and more quadrate towards the apex. Perichætial leaves, outer with a broad base suddenly contracted into a long narrow point, innermost lanceolate, amplexicaul, all nerved to apex. Seta thin, ferruginous, length ¼in.–1in. Capsule leptodermous, erect, symmetrical, oval, exannulate, ferruginous. Operculum and calyptra not seen. Peristome of 16 teeth, short, papillose, thin, indistinctly barred, the lower part yellow, hyaline above. Male inflorescence gemmaceous, axillary below the perichætial leaves, bracts concave, ovate - acuminate, antheridia long, mixed with numerous paraphyses.

Hab. On rocks. A very distinct and beautiful species, belonging to a genus not hitherto recorded in New Zealand.

Log. Kaikoura; No. 263 (named by Dr. Müller). Benmore, 4,000ft.; No. 295. On the ground, Kowai; T. W. N. B. Mount Earnslaw; W. Bell.

Pottia marginata, sp. nov. Plate XXXV.

Synoicous. Cæspitose, minute, simple or dichotomous, olivegreen, leaves, lower ovate-lanceolate, upper elongato-lingulate, acuminate, carinate, not narrowed below; nerve brown, stout, tapering at the apex and excurrent in a point; margin flat, bordered by four rows of long clear yellow cells, vanishing before reaching the apex, which is coarsely and irregularly dentate. Cells at the base and of one-third of leaf oblongohexagonal, hyaline, gradually merging into small, roundish, hexagonal, opaque, densely chlorophyllose cells. Seta stout, short; capsule gymnostomous, erect or slightly inclined, long-oval, gradually tapering into the seta, chestnut-brown, smooth, contracted at the mouth when dry; operculum conicorostrate; calyptra covering the whole of the capsule, campanulate, base closely clasping the seta until near maturity, when

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by the growth of the capsule it splits and becomes cucullate, cartilaginous, smooth. Inflorescence: ♂ and ♀ mixed together in the same inflorescence.

Hab. On clay banks.

Loc. Cachmere Road, Lyttelton Hills; October, 1887; No. 57. On dead “nigger-heads,” Wairarapa Stream, Fendalton; July, 1889; T. W. N. B. Christchurch Domain Garden; T. G. Wright. Mungatui; September, 1887; W. Bell. Pine Hill, near Dunedin; January, 1890, No. 275 (named by Dr. Müller); W. Bell.

In an immature state the calyptra covers the entire capsule and tightly clasps the seta, as in the genus Calymperes, but on nearing maturity the growth of the fruit ruptures the very cartilaginous calyptra, when it becomes truly cucullate, and is pushed upward, covering only two-thirds of the capsule. The plant is therefore a true Pottia.

Orthotrichum graphiomitrium, sp. nov. Plate XXXVI.

Autoicous. Stems subrepent or laxly pulvinate; branches erect, 1in.–1.¾in. long, more or less branched. Leaves laxly imbricated, patent, when dry appressed but not much altered; stem-leaves oblong-lanceolate, gradually acuminate, comal leaves larger, perichætial leaves longer and narrower than the comal ones. Nerve stout, carinate, vanishing within the apex; margins quite flat. Cells at the base long, yellow, above round, distinct, papillose. Capsule on a very short seta, hardly visible above the leaves, ovate, smooth, striæ very indistinct, narrowed gradually below. Stomata on lower part of capsule superficial, large. Operculum conic, rostellate, with a red line round the base. Calyptra conic, golden-yellow, darker at the apex and base, covered with long, jointed, pale-yellow hairs, plicate, base lobed. Peristome, outer of 8 teeth bigemmate, greyish-orange, obtuse, cilia 8, nearly as long as the outer teeth, broad, consisting of two rows of cells, palegrey. Male inflorescence gemmiform, axillary in the lower leaves of fertile branches, bracts ovate-obtuse, nerved threequarters, cells of lower half brown, antheridia about 12, paraphyses few or 0.

Hab. On the stems and branches of small trees at high elevations.

Loc. Arthur's Pass, 3,013ft.; No. 176 (named by Dr. Müller). On “ribbonwood” trees, Benmore; T. W. N. B.

This very handsome and distinct moss, often of a brightgolden colour, is extremely local, but very abundant in places where it is found. The subrepent mode of growth is unusual in Orthotrichum. It creeps along branches with quite the habit of Macromitrium, and forms patches 7in. or 8in. long.

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Zygodon integrifolius, sp. nov. Plate XXXVII.

Autoicous. In soft, dense, green cushions, dark-brown below, sparingly branched. Leaves patent and recurved, curled and contorted when dry, linear, very acuminate, keeled; margins plane, quite entire, nerve stout, concolorous, vanishing within the apex. Cells at the base rectangular, not hyaline, gradually merging into minute, square, somewhat obscure cells. Perichætial leaves long, ovate, tapering gradually to a fine point, cells rectangular, uniform over the whole leaf. Seta short, curved. Capsule gymnostomous, just showing above the leaves, oval-pyriform, brown, marked with 8 darker striæ, when dry contracted below the mouth, grooved, urceolate. Operculum flat, with a blunt oblique beak. Calyptra small, cucullate, only covering the top of the capsule, fugaceous. Male inflorescence gemmaceous, axillary below the perichætial leaves, bracts 3—4 ovate-acuminate, nerved, antheridia few, paraphyses none.

Hab. In crevices and fissures of rocks in sheltered situations.

Loc. Benmore, Canterbury; alt., 4,000ft.; November, 1890; No. 297 (named by Dr. K. Müller). Thirteen-mile Bush; September, 1892. Studholme Bush, Waimate; April, 1892; T. W. N. B. Glenorchy, Lake Wakatipu; January, 1890; W. Bell.

Nearly allied to the European Zygodon lapponicus, B. and S.

Climacium novæ-seelandiæ, sp. nov. Plate XXXVIII.

Primary stem creeping, sending up erect dendroid stems, which are densely covered with matted roots and broad closely-appressed leaves. Branches generally simple, sometimes slightly pinnate, growing on all sides round the top of the stem, the lower branches longest. Leaves thickly inserted all round the branches, plicate, margins flat. Leaves of stem broad, cordate at base, the apex rounded, very concave, quite entire, nerved three-quarters of their length. Branch-leaves from a cordate base, broadly ovate, concave, tapering towards the apex, obtusely pointed, almost entire, nerve vanishing within the apex. Leaves towards the ends of the branches and of branchlets narrower ovate-lanceolate, apex obtuse and very coarsely toothed, nerve vanishing within the apex. Cells slightly enlarged at the basal angles; the cells at the base of the leaf bright yellow-brown; cells of leaf long, ends pointed. Fruit not seen.

Loc. Castle Hill, North Canterbury; T. Kirk.

This handsome moss has the habit and appearance of the European Climacium dendroides. The leaves are, however, different.

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Andreæa cochlearifolia, sp. nov. Plate XXXIX.

Dioicous (?). In dense blackish-brown tufts. Stems 1.½in. long, 1 line in diameter, sparingly branched, lower parts denuded. Leaves loosely imbricated, inflated, cochleariform, oval or ovate, margins flat in the upper half and not concave, entire, apex minutely apiculate, dull olive-green, nerve broad, vanishing about the middle of the leaf. Perichætial leaves long-ovate, convolute. Cells at the base long, yellow, rather opaque, forming a circular patch not extending to the margins; cells of leaf small, quadrate, becoming roundish towards the apex, not papillose. Capsule entirely exserted, cleft from base to apex into 4 or 6 valves, dark-purple male inflorescence, bracts 3, antheridia about 5, paraphyses 0.

Hab. Wet rocks, under dripping water.

Loc. Mount Bonpland; alt., 4,000ft.; Otago; No. 353; W. Bell (named by Dr. Müller).

Quite distinct from any hitherto-described New Zealand Andreœa, and growing in situations—in water—very unusual for species of this genus. The nerve is not of greater thickness than the leaf, and is composed of a number of rows (from 10 to 20) of long opaque cells, which branch off in a fan-shaped manner about the middle of the leaf, and are lost amongst the leaf-cells. The margin of the upper part of leaf is flattened out like the edge of a plate.

Andreæa pulvinata, sp. nov. Plate XL.

Dioicous. Densely pulvinate in large hemispherical masses, purplish-red, dichotomously branched. Stem 1.¼in. to 1.½in. long. Leaves distant, patent, small, ovate-lanceolate gradually tapering to a blunt point, nerveless; comal leaves larger, more or less falcato-secund; perichætial leaves large, broad, ovate, tapering to an obtuse point, convolute. Cells at the base, in the centre, but not extending to the margins, long, squareended, of a rich orange-purple, leaf-cells regular, dot-like, and strongly papillose at the back. Male inflorescence in a round bud, bracts 3, very concave, orbicular, pointed, antheridia 2 or 3, paraphyses none.

Hab. On south-east faces of rocks.

Loc. Rockwood, North Canterbury; November, 1890; No. 359 (named by Dr. Müller).

A very distinct species. The male plant shows the inflorescence of past years like beads upon a string. The inflorescence is truly terminal, though apparently lateral through being pushed aside by the new shoot which is developed im mediately below the bracts.

Andreæa arctoæoides, sp. nov. Plate XLI.

Dioicous. In fragile dark-green or brownish tufts. Stems 4 to 9 lines long, simple or fastigate. Leaves spreading,

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crowded, orange-yellow, apices darker, appressed when dry, oval, suddenly attenuated and tapering into a long point, which is sometimes slightly falcate; nerve indistinct, darker coloured, vanishing in the narrowed part; perichætial leaves 3 or 4, large oval, suddenly contracted into a narrow point one-third the length of the whole leaf, faintly nerved half-way; cells of centre of the leaf at base and on each side of nerve long and narrow, leaf-cells oval, small. Capsule 4-valved, oval, not exserted beyond the apex of leaves. Male inflorescence—bracts ovate, narrowed into a small point, antheridia few, paraphyses numerous, long, thin, smooth, the joints very inconspicuous, dark-orange.

Hab. On rocks.

Loc. Rockwood, North Canterbury; November, 1890; No. 371 (named by Dr. Müller). Mount Torlesse; April, 1892; No. 412; T. W. N. B.

Quite distinct from A. pulvinata in its mode of growth and form of leaves.

Hypnum (Heterophyllum) kirkii, sp. nov. Plate XLII.

Minute, growing in dense close cushions, stems irregularly branched. Leaves greyish-green, not much altered when dry, linear, lanceolate, gradually attenuated from the base to a slender point, apex minutely serrated, nerveless, base of leaf concave, with flat hyaline alæ with large hyaline cells, cells at centre of base distinct bright yellow, cells of leaf long, distinct, slightly sygmoid; perichætial leaves much larger, erect, outer ovate-acuminate entire, inner ovate-lanceolate gradually tapering to a fine point very slightly denticulate at the apex, lower half of all bright yellow. Seta smooth, 5 lines long, brownish-red, vaginula large, turbinate. Capsule slightly inclined, oval. Operculum conic, with a long attenuated beak. Peristome, teeth pale yellow, lanceolate, subulate, inner surface very trabeculate, endostome consisting of 16 carinate imperforate processes without intermediate cilia.

Hab. Growing on trees and decayed bark.

Loc. The Snares; No. 370; T. Kirk; 1890 (named by Dr. Müller). Paterson's Inlet, Stewart Island; T. Kirk; 1890.

Fissidens (Heterocaulon) ramiger, sp. nov. Plate XLIII.

Rhizantoicous, solitary or gregarious, minute. Fertile stems very short; leaves few, two inner ones convolute round the seta, apex produced into a long point; lower ones (2 or 3) smaller, diminishing in size; the vaginant laminæ occupying nearly the whole of the leaf, the superior lamina very short and narrow, and curved into a beak. Barren stems—leaves 8–10-jugous, lower smaller shorter and ovate, ovate-lanceolate

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towards the upper part of stem; vaginant laminæ two-thirds the length of leaf; inferior lamina narrow, vanishing before the base, nerve thick, vanishing in the apex, immarginate, entire. Cells large, irregular, hexagonal. Seta short, stout, yellow, three times the length of capsule. Vaginula very wide. Capsule oval, symmetrical, erect or very nearly so. Operculum not quite half the length of capsule, conic, apiculate. Peristome red, teeth cleft to the middle into two long filiform legs, undivided part strongly trabeculate. Male inflorescence gemmiform, situated at the base of the fertile stems, amongst the roots.

Hab. On clay.

Loc. Lyttelton Hills; No. 376 (named by Dr. Müller). On sod-banks, Malvern Hills; September, 1892.

In some specimens the margin of the vaginant laminæ has a slight border of long cells. In several instances I have observed twin setæ in one inflorescence.

Fissidens (Bryoidium) campyloneurus, sp. nov. Plate XLIV.

Dioicous(?). Densely gregarious. Very small, simple, leaves pale yellowish-green, crisped when dry, lanceolate, very acute, vaginant laminæ half the length of leaf, inferior lamina narrowed below and vanishing towards the base; nerve stout, with a considerable bend where it passes below the vaginant laminæ, which it encircles on the inner side, continued to the apex, where it unites with the border, which is continuous round the whole of the leaf; border composed of two or more rows of long paler cells; leaf-cells rounded-hexagonal, distinct. Barren shoot 7–9-jugous. Fertile stems, 3–plurijugous, procumbent, causing the erect seta to have a bend close to the vaginula; leaves linear-lanceolate, longer and narrower than on the barren shoots, the two perichætial leaves longest. Seta pale-red, slender, flexuous. Capsule short, oval, erect or slightly inclined, contracted below the mouth when dry. Operculum conic, with a straight blunt beak. Peristome deep brownish-red, not inserted below the mouth, teeth cleft two-thirds into two slender legs, the lower undivided portion closely and strongly trabeculate, the bars on the legs placed diagonally, giving them a spirally-twisted appearance.

Hab. On damp clay.

Loc. Waimate, South Canterbury; No. 150 (named by Dr. Müller). Mount Fife, Kaikoura; No. 267. Benmore; alt., 4,000ft. Patterson's Creek, Mount Torlesse; T. W. N. B. Pine Hill, Dunedin; W. Bell.

In the apical leaves of barren plants the border and nerve vanish towards the apex, though in the lower leaves

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on the same branch they are well defined to the extreme point. Resembling F. viridulus, Wähleub, from which it is distinguished by the peristome, which in viridulus arises from below the mouth of the capsule. The peculiar twist in the nerve, which is a very constant character, also separates the two species.

Explanation of Plates XXXIV.–XLIV.

Plate XXXIV.—Blindia chrysea.

  • Fig. 1. Plant, natural size.

  • " 2. Leaf, X 32.

  • " 3. Cells near base, X 270.

  • " 4. Cells from centre of leaf, X 270.

  • " 5. Cells from apex, X 270.

  • Fig. 6. Perichætial leaf, X 32.

  • " 7. Ripe capsule, X 37.

  • " 8. Peristome, X 270.

  • " 9. Male inflorescence, X 32.

  • " 10. Antheridia and paraphyses, X 70.

Plate XXXV.—Pottia marginata.

  • Fig. 1. Plant, natural size.

  • " 2. Leaf, X 32.

  • " 3. Marginal cells, X 270.

  • " 4. Apex of leaf, X 270.

  • " 5. Cells from base of leaf, X 270.

  • " 6. Cells, transitional from hyaline to chlorophyllose, X 270.

  • Fig. 7. Immature capsule, showing the calyptra covering the whole fruit and clasping the seta, X 12.

  • " 8. Ripe capsule with calyptra, X 32.

  • " 9. Operculum, X 32.

Plate XXXVI.—Orthotrichum graphiomitrium.

  • Fig. 1. Stem-leaf in profile, X 32.

  • " 2. Comal leaf, X 32.

  • " 3. Apex of leaf, X 70.

  • " 4. Cells at base, X 270.

  • " 5. Leaf-cells, X 270.

  • " 6. Capsule, X 12.

  • Fig. 7. Calyptra, X 12.

  • " 8. Base of calyptra, X 70.

  • " 9. Stomata, X 270.

  • " 10. Peristome, X 70.

  • " 11. Operculum, X 32.

  • " 12. Male inflorescence, X 32.

Plate XXXVII.—Zygodon integrifolius.

  • Fig. 1. Plant, natural size.

  • " 2. Leaf, X 32.

  • " 3. Apex of leaf, X 270.

  • " 4. Basal cells, X 270.

  • " 5. Leaf-cells, X 270.

  • " 6. Perichætial leaf, X 32.

  • Fig. 7. Capsule, X 32.

  • " 8. Old and dry capsule, X 32.

  • " 9. Operculum, X 32.

  • " 10. Male inflorescence, X 70.

  • " 11. Bract and antheridia, X 70.

Plate XXXVIII.—Climacium novœ-seelandiœ.

  • Fig. 1. Plant, natural size.

  • " 2. Stem-leaf, X 32.

  • " 3. Leaf from main branches, X 32.

  • Fig. 4. Alar cells, X 270.

  • " 5. Leaf-cells, X 270.

  • " 6. Leaf from branchlet, X 32.

  • " 7. Apex of same, X 70.

Plate XXXIX.—Andreœa cochlearifolia.

  • Fig. 1. Plant, natural size.

  • " 2. Comal leaf, X 32.

  • " 3. Stem-leaf, X 32.

  • " 4. Apex of leaf, X 70.

  • " 5. Cells at apex of leaf, X 270.

  • Fig. 6. Leaf-cells, X 270.

  • " 7. Capsule, X 12.

  • " 8. Male bract and antheridia, X 70.

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Blindia chrysea. sp. nov

.

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Pottia marginata. sp. nov.

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Orthotrichum graphimitrium. sp. nov.

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Zygodon integrifolius. sp. nov.

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Climacium Novœ-Seelandiœ sp. nov.

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Andreœa cochlearifolia. sp. nov.

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Andreœa pulvinata. sp. nov.

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Andreœa arctoœoides. sp. nov.

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Hypnum Kirkii sp. nov.

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Fissidens ramiger sp. nov.

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Fissidens campyloneurus. sp. nov.

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Plate XL.—Andreœa pulvinata.
  • Fig. 1. Plants, natural size.

  • " 2. Leaves, X 32.

  • " 3. Comal leaf, X 32.

  • " 4. Perichætial leaf, X 32.

  • " 5. Cells from base of leaf, X 270.

  • Fig. 6. Leaf-cells, X 270.

  • " 7. Papillæ from back of leaf, X 270.

  • " 8. Male inflorescence, X 70.

  • " 9. Bract and antheridia, X 70.

Plates XLI.—Andreœa arctoæoides.
  • Fig. 1. Plants, natural size.

  • " 2. Leaves, X 32.

  • " 3. Perichætial leaf, X 32.

  • " 4. Part of nerve and adjacent cells, X 270.

  • Fig. 5. Leaf-cells, X 270.

  • " 6. Male bract, X 32.

  • " 7. Paraphyses, X 270.

Plate XLII.—Hypnum kirkii.
  • Fig. 1. Plant, natural size.

  • " 2. Leaf, X 32.

  • " 3. Leaves, X 70.

  • " 4. Apex of leaf, X 270.

  • " 5. Base of leaf, X 270.

  • " 6. Outer perichætial leaves, X 32.

  • Fig. 7. Capsule and operculum, X 32.

  • " 8. Vaginula, X 32.

  • " 9. Peristome, X 70.

  • " 10. Endostome, X 70.

Plate XLIII.—Fissidens ramiger.
  • Fig. 1. Plants, natural size.

  • " 2. Barren plant, X 32.

  • " 3. Fertile plant, X 32.

  • " 4. Male inflorescence, X 32.

  • " 5. Perichætial leaf, X 32.

  • Fig. 6. Leaf, X 32.

  • " 7. Apex of leaf, X 270.

  • " 8. Leaf, X 70.

  • " 9 and 10. Capsule and operculum, X 32.

Plate XLIV.—Fissidens campyloneurus.
  • Fig. 1. Plants, natural size.

  • " 2. Leaves, X 32.

  • " 3. Apex, X 270.

  • " 4. Perichætial leaf, X 32.

  • " 5. Leaf from middle of barren stem, X 270.

  • Fig. 6. Leaf from apex of the same stem, X 270.

  • " 7, 8, 9. Capsules, X 32.

  • " 10. Tooth of peristome, X 270.

Art. XXXVII.—On some Little-known New Zealand Mosses.

[Read before the Philosophical Institute of Canterbury, 2nd November, 1892.]

Since the publication of the “Handbook of the New Zealand Flora” in 1867 many additions have been made to our mossflora; and it is the object of this paper to put on record as having been found in New Zealand species which have already been published from other countries.

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In 1889 Mr. William Bell, of Pine Hill, Dunedin, sent a collection of mosses, chiefly belonging to the family Orthotricheœ, to Mr. Mitten for identification. Mr. Bell has kindly placed Mr. Mitten's letter and notes at my disposal, and supplied me with type specimens of the mosses. Mr. T. Kirk has lately allowed me to examine an interesting collection of seventy-nine Westland mosses, made by Mr. R. Helms, of Greymouth, in 1882. They were sent that year to Dr. Karl Müller for determination, and he decided that thirty-six were new to science. These he has named; but he tells me, in a letter which I have recently received from him, that they have not yet been described, and have not been published.

With the material these collections afforded me, and a few mosses derived from other sources, I am enabled to enumerate fourteen mosses not hitherto included in the New Zealand flora.

Blindia robusta, Hampe.

“Cæspitosa, robusta, sesquiuncialis parce ramosa, folia maxime falcata integerrima, nervo plano evanescente, cellulis linearibus versus apicem densioribus flavescentibus, echlorophyllosis, alaribus grandibus subquadratis hyalinis; seta crassa semiuncialis flavescens, theca subrotundo-ovalis, coriacea fusco-rubra suberecta, operculo conico-obliquo crasso subulto thecam dimidiam æquante pallidiore, dentibus peristomii latioribus membranaceis inflexis plus minusve regulariter divisis. Hab. In Alpibus Austr., Mount Munyang.”—“Linnæa,” 1859–60, p. 627. F. von Müller's “Analytical Drawings of Australian Mosses,” tab. 7.

Autoicous. Male inflorescence bud-like, terminal in a branch below the female inflorescence, bracts obovate abruptly contracted into a lanceolate point, antheridia numerous (23).

Hab. On old moraine at the base of the Waimakariri Glacier; 1889; R. Brown.

I have authentic specimens of B. robusta from Mr. Sullivan, collected in snowy watercourses, Mount Kosciusko, New South Wales, which enabled me to identify this moss.

Grimmia leucophæa, Greville, in Trans. Werner Soc., iv., f. 6. Grimmia leiocarpa, Taylor.

Readily known from the other New Zealand species of Grimmia by its very rough hair-points. A cosmopolitan species.

Hab. On boulders, Dyer's Pass, Lyttelton Hills; No. 114; 1888; T. W. N. B. Banks of the Clutha, Otago; 1891; W. Bell.

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I have this moss also from the Barossa Range, South Australia, Tepper; and from Queensland, Bailey.

Anomodon huttonii, Mitten.

“Caulis procumbens, ramis ascendentibus subpinnatim divisus; folia caulina patentia, ovata, acumine lato apice acutiusculo, nervo indistincto supra medium evanido, ramea subcompressa, basi subovata, ligulata, acutiuscula, omnia inferne canaliculato-concava, apicem versus plana, cellulis rotundis obscuris papillosis, margineque crenulata. Hab. New Zealand, Great Barrier Island; Hutton et Kirk.” —Mitten, Journ. Linn. Soc., vol. xiii., p. 309.

As Mr. Mitten's description of this interesting moss was published in his paper on Ceylon Musci, and may be overlooked, I reproduce it here.

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

The branches are extremely filiform, 4—6 lines long; when dry julaceous and not more than 8/1000in. in diameter, with the leaves closely appressed. When moist the leaves are patent. The cells are large, roundish-hexagonal, and very uniform in size over the whole of the leaf. There are a few long cells on each side of the nerve at its base. The nerve, from a broad base, tapers, and vanishes above the middle of the leaf. Each individual cell projects at the edge of the leaf, causing the margin to be minutely crenulate.

Mr. Kirk, to whom I am indebted for this moss, informs me that he found it but sparingly on the Great Barrier, but freely at Omaha and Matakana, and other places in Auckland.

In “Herb. Bell,” identified by Mr. William Mitten.

Tortula muralis, Hedwig.

A very cosmopolitan plant, but not before recorded as found in Australasia. On chimney, Pine Hill, near Dunedin; W. Bell; No. 649.

Orthotrichum rupestre, Schleich.

On rocks, Mount Earnslaw; 1890; W. Bell. Mount Benger, 4,000ft.-5,000ft., and Pine Hill; W. Bell; No. 265; 1887. Mount Fife, Kaikoura; T. Kirk; 1889. Benmore, alt. 4,000ft.; T. W. N. B.; 1890.

Orthotrichum tasmanicum, H. f. and W. (London Journ. Bot., vii., 1848, p. 27.) Flora Tasm., ii., 184.

On twigs of bushes (especially Discaria toumatou); not uncommon. Lake Wakatipu and Pine Hill; W. Bell; Nos. 438, 646; 1888. Mount Torlesse, 1892; Hunter's Hills, Waimate; Little River, Akaroa, 1887; T. W. N. B.

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Zygodon minutus, Hampe and C. Müll. (“Linnæa,” 1856, p. 209). Flora Tasm., ii., 186.

Found in Australia and Tasmania. Paterson's Inlet, Stewart Island; W. Bell; No. 674a; 1889. On the bark of ngaio trees (Myoporum lœtum), Maungamana Bay, Kaikoura; 1889; T.W. N.B.

Eucamptodon inflatus, Mitten. Hypnum inflatum, H. f. and W. Fl. N.Z., ii., tab. 90, fig. 5.

“I send a stem of the Hypnum inflatum of Fl. N.Z. No fruit has been seen. I keep it as a species of Eucamptodon which is almost the same as Dicnemon: but Eucomptodon has an erect capsule; in the other genera it is curved and unequal. These are dicranoid mosses, having no affinity with Hypna of any kind. Eucamptodon inflatus is the finest species yet discovered. In both genera, Dicnemon and Eucamptodon, the primary stem is creeping, from which fertile branches arise.”—W. Mitten in litt.

Great Barrier Island; T. Kirk. Near Auckland; T. F. Cheeseman.

In “Herb. Helms,” identified by Dr. Karl Müller.

Hypnum (Hypnodendron) deflexum, Wilson.

This is Isothecium arbusculum, var. β deflexum, Fl. N.Z., ii., 104; Hypnum deflexum, C. Müll., Syn. ii., p. 680. Mr. Mitten considers this moss distinct from Isothecium arbusculum,” Australian Mosses,”.p. 35.

Found in New South Wales and Tasmania. “Herb. Helms,” No. 3.

Hypnum (Rhynchostegium) huttoni, Hampe.

Nearly allied to Rhynchostegium tenuifolium, Hed. Autoicous, male inflorescence bud-like in the axils of leaves below the female inflorescence.

Westland, “Herb. Helms,” No. 16. Pine Hill, Dunedin; W. Bell; No. 657; 1888. Greymouth; W. J. Gulliver. Barry's Pass, Akaroa; T. W. N. B.; No. 55; 1887.

Pilotrichella billardieri, Hampe (“Linnæa,” 1859, Neckera).

Meteorium billardieri, Mitten, “Australian Mosses,” p. 34.

Found in Gippsland: F. v. M. It very much resembles a large form of M. molle. “Herb. Helms,” No. 41. Kaikoura, No. 13b, identified for me by Dr. Müller. Oxford Bush, North Canterbury; T. W. N. B. Nelson; D. Grant.

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Rhizogonium aristatum, Hampe.

“Gracillimum, laxe cæspitosum, unciale, adscendens. Caulis filiformis basi nudus vel foliis parvis remotis ovatis cuspidatis munitus, superne foliis approxumatis, anguste plumiformis flavescens. Folia disticha, oblique inserta, unolatere patenti concava, e basi parce obovata late lanceolata, planiuscula, margine flavescenti limbata, versus apicem remote dentata, nervo lutescente solido aristata, cellulis angulatorotundatis parce incrassatis, pallide diaphanis. Folia perichætialia lanceolato-subulata elongata subintegerrima vel parce denticulata erecta, apice pallida, nervo percursa longius aristata. Seta basilaris erecta sesquiuncialis caulem superans, apice incrassata rubra. Theca læsa horizontalis oblonga annulata peristomio? Lake Pedder, Tasmaniæ; parcissime legit Schuster. Rhizogonio novœ-hollandiœ simillimum, sed foliis limbatis primo visu discernendum.”—“Linnæa,” xl., 1876, p. 314.

Greymouth, in “Herb. Helms,” No. 49. Westland; T. Kirk. Stewart Island, on stems of tree-ferns; W. Bell; No. 715.

Dicranum (Campylopus) capillatus, H. f. and W. Flora Tasm., ii., 172.

A Tasmanian moss nearly allied to Campylopus appressifolius. Westland, in “Herb. Helms,” No. 64.

Dicranum (Campylopus) leptocephalum, C. Müll. (“Linnæa,” 1855, p. 206).

Mitten, in “Musci Austro-Americani,” Jour. Lin. Soc., xii., p. 84, gives this as a synonym of Campylopus introflexus, Hed., and remarks, “C.introflexus is very variable in external appearance—in the colour of the leaves, and in the length and curvature of their white points.” “Herb. Helms,” No. 73.

Bartramia commutata, Hampe.

“Dioica, robusta, vage ramosa, decumbens. Caulis fere ubique rufo-tomentosus, fructifer adscendens, superne radiatus, flavescens, ramis teretibus acutis, caulis masculus subsimplex, apice stellatus. Folia caulina sicca accumbentia humido erecto-patula, e basi contracta concava pluries plicata, late ovato-lanceolata subintegerrima, nervo percursa setaceo-aristata, margine toto revoluto, cellulis abbreviato-parallelogrammicis, nodulis minimis interrupto-punctatis, basi latere velo tenero latiore reflexo, cellulis quadratis reticulato pellucido aucta. Radiorum folia minora, magis pellucida, tenerrime reticulata, evidenter scabra, nervo tereti lutescente in subulam

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denticulatam excedente. Folia perichætialia interiora parva, ovato-lanceolata nervosa, brevius aristata, profunde plicata, hyalina, cellulis rectangulis lævibus reticulata. Seta vix uncialis adscendens rubens apice inclinata. Theca junior sphærica, deinde nutans, oblonga, sicca paulisper striata; operculo breve conico obtuso. Peristomium inflexum parvulum sanguineum, dentibus exter. anguste lanceolatis acuminatis dense trabeculatis; intern. cruribus ovato-acuminatis, ciliis brevissimis.

“Mount Grampians; leg. W. Sullivan.

“Syn. Bartramia affinis, Schwæg., tab. 237, mala; nec Hooker, tab. 176. In Tasmania, in montosis versus lacum Pedder, 1875, legit Schuster formam minorem vix biuncialem.”—“Linnæa,” 1876, p. 307.

Nearly allied to B. affinis. Mitten, in “Australian Mosses,” p. 21, considers it a distinct species. Westland, in “Herb. Helms,” No. 68.

Art. XXXVIII.—On a New Insectivorous Plant in New Zealand.

[Read before the Wellington Philosophical Society, 7th December, 1892.]

As is probably well known to all present, we possess in New Zealand several species of Drosera, a group of plants which not only catch insects by means of their tentacles and the viscid matter secreted from their glands, but which, as Darwin has conclusively shown, have likewise the power of dissolving animal matter by the aid of this secretion, which contains an acid, together with a ferment almost identical in nature with pepsin, the matter thus digested being afterwards absorbed into the system of the plant as a means of nourishment. Darwin has fully described other insect-catching plants—Drosophyllum, Roridula, and Byblis effecting the capture by means of their viscid secretion alone, and Dionœa and Aldrovanda through the rapid closing of their leaves. All these carnivorous plants belong to a recognised family known as the Droseraceœ, comprising six well-determined genera.

The New Zealand plant which I desire to bring under your notice to-night is something entirely different. It is a species of fungus belonging to the genus Aseroe, described thus in Hooker's Handbook (vol. ii., p. 616): “A curious genus, the arms of whose pileus somewhat resemble a starfish. Found in New Zealand, Ceylon, and Australia. Volva globose, gela-

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tinous within; pileus stalked, divided at the summit into long radiating simple entire or forked horizontal arms; hymenium at the base of the arms.” The species to which I am about to refer is thus described by the same distinguished botanist:—

Aseroe rubra, Labill., Fl. N. Holl., ii.; Berk., in Fl. N.Z., ii., 187. Two to four inches high; stem as thick as the thumb, even. Rays of the pileus about 8, bright-red, long, subulate, lin.–2in. long, split to the base, continuous with the stem, not divided from them by a deep groove.”

Another species of the same genus, discovered by Mr. Colenso at the Bay of Islands, has been described, and named Aseroe hookeri; but I have never seen it.

There is an excellent coloured drawing of Aseroe rubra in the appendix to the Rev. Richard Taylor's “New Zealand and its Inhabitants” (pl. v., fig. 3).

I have met with this plant in various parts of New Zealand, always in the depth of the woods, its star-like form and bright colour attracting immediate notice. But what I desire to call attention to now is the singular fact (hitherto unrecorded) that this fungus appears to be insectivorous in its habit of life. Its presence is always indicated by a peculiar fœtid smell, like decomposing animal matter, and so pungent in its nature that on handling the plant this very disagreeable odour communicates itself to the fingers, and can only be got rid of by washing the hands in water.

On a recent occasion I found several of them growing in the woods near the Papaitonga Lake; and Mr. Morgan Carkeek, the District Surveyor, who happened to be with me at the time, drew my attention to the fact that each of them had the surface-cup, if I may so term it, completely filled up with the partially-dissolved bodies of dead insects. Mr. Carkeek assured me that during the many years he has spent in the New Zealand forests he has invariably found this plant garnished in a similar manner.

From the interior of the stem a viscid foul-smelling fluid is secreted, and this rises into the cup and mixes with the bodies of moths, flies, beetles, and other small insects collected there, which appear to undergo a process of gradual dissolution and absorption. Now, the question arises, Is this fungus, like the Drosera, a carnivorous plant, and is it endowed with its pungent odour, added to its flower-like brilliancy, for the purpose of attracting its insect-food? And is the fluid itself a solvent, with the acid constituent for aiding the process of digestion? My answer is in the affirmative.

I dissected one of the stems, and found that it was hollow, or nearly so, with what appeared to be a membranous sac at the bottom containing fluid matter; but the examination,

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made on the spot, was necessarily a very hasty and imperfect one.

Since the above was written I have received a letter from Mr. J. Brough, of Nelson (a very observant settler), forwarding me a pressed specimen of the star-like portion of the plant, which I now exhibit, and accompanied by the following note:—

“I wish to bring under your notice a rare fungus I met with some time ago in the locality of Rotoiti Lake. I have never noticed anything of the kind in my travels before. There were six of them, forming a sort of circle. They had the appearance when growing of a flesh-and-blood colour, and several insects and spiders were sticking about each of them. I preserved three of them, and I send you one herewith. Of course it is now dried up, and you merely get the outline, but no doubt this will be sufficient to enable you to send me its botanical name.”

Art. XXXIX.—Botanical Notes from Takaka District.

[Read before the Nelson Philosophical Society, 28th March, 1892.]

The ferns which I exhibit this evening are a portion of those I collected during a recent trip to the Takaka district in company with Mr. W. H. Bryant, of Brightwater.

We carried our tents and provisions ourselves without the aid of a horse, and could therefore stop where and when we chose. For real enjoyment and effective work this method, although somewhat laborious, has many advantages over the customary trap or pack-horse.

On our trip we touched at the Tata Islands, and walked from Waitapu by Rangihaeata Point and Anahau to Puramahoi, thence back to Motupipi, thence up the Takaka Valley over the range to Motueka.

The following are the most rare specimens collected or noted on the trip:—

Schizea bifida. Between Takaka and Puramahoi. This has not been hitherto recorded as found in this part of New Zealand.

S. fistulosa. Very plentiful near Takaka.

Lycopodium laterale. Near Takaka; not very common.

Hymenophyllum tunbridgense. Fine examples on Takaka Ranges.

H. tunbridgense, var. unilaterale. Also on Takaka Ranges.

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H. malingii. This beautiful fern is fairly plentiful on the top of the range.

H. rufescens. Also growing on the top of the range.

H. demissum and subtilissimum. Of these, exceedingly large and fine specimens were collected.

Trichomanes strictum and rigidum. Both forms were growing luxuriantly near Puramahoi; so also was

T. colensoi, near the same locality.

Cystopteris fragilis. Good specimens of this beautiful fern were obtained on the limestone, Takaka Ranges.

Lindsaya linearis, trichomanoides var. lessoni, Pteris scaberula, tremula, incisa, and macilenta, were also fairly plentiful.

Lomaria nigra and fraseri. Some remarkably fine specimens were collected at Puramahoi.

Gleichenia flabellata. Growing near Takaka. This is quite new to this Island.

Asplenium trichomanes, obtusatum, var. lyalli, and umbrosum. Also noticed the latter abundant in Takaka Valley.

Todea superba and Botrychium ternatum. Very fine specimens of both between Takaka and Riwaka.

Lycopodium billardieri between 5ft. and 6ft. long, and Tmesipteris forsteri over 4ft. long, were collected, and I now exhibit specimens.

Mr. Bryant also found Senecio laxifolia and Arthropodium cirrhatum in flower, although so late in the season.

In conclusion, I should like to add that the district appears to be a perfect paradise for a botanist. The people are kind and hospitable, and the weather we experienced was almost perfect. The bush scenery is quite charming—that is, where the axe of the settler has not yet destroyed it, or the fire-loving vandals of these colonies have not desecrated it. One thing afforded great pleasure, and that was the presence of many little native birds; whereas in the neighbourhood of Nelson one rarely sees any, in consequence of the supineness of the authorities to the wilful destruction by guns and catapults in the hands of boys, who at every opportunity sally forth to gratify their bloodthirsty proclivities by taking the lives of those confiding insectivorous birds, designed by Nature to restrain the increase of insect pests. The destruction of these birds in the near future, I am convinced, will be looked upon as an irreparable calamity.

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Art. XL.—On a Remarkable Variation in Lomaria lanceolata.

[Read before the Nelson Philosophical Society, 28th March, 1892.]

The plant which forms the subject of this short paper (and of which I exhibit specimens) was collected by Mr. W. H. Bryant and myself on the north-western slope of “Little Ben,” a hill whose altitude is about 2,884ft., and situate some seven or eight miles up the Wairoa River.

Our visit was a very short one. We ascended the hill on the morning of the 1st January last, and stayed one night only, and this short stay was further limited by rain on the forenoon of the 1st. Nevertheless we saw much of interest, and the trip was thoroughly enjoyable.

In a well-wooded gully we found a number of plants of Lomaria lanceolata, and in one spot, for a distance of about three or four yards, we found the greater portion of them showing a tendency to vary: some showed a bifurcate tendency, others trifurcate, and in two cases a quadrifurcate variation. We did not in any plant find every frond furcated, but in one specimen I noticed eight fronds, both fertile and sterile, which had varied in one direction or another.

It was curious to notice that nowhere else could we discover any tendency to vary, although this species of Lomaria was abundant.

I communicated the fact to Mr. Kirk, and furnished him with specimens, and he informs me that he has no previous record of a tendency to vary in Lomaria lanceolata.

Mr. W. H. Bryant is attempting to propagate this variety from the spores.

In the Wairoa Valley I also noticed a remarkable case of reversion in Pseudopanax ferox. At about 12ft. from the ground, in a tree whose diameter was over a foot, there is a tuft of those peculiar and strikingly ornamental leaves of the young-plant type.

On the side of Little Ben I gathered a specimen of fungus which Mr. Kirk tells me is new to New Zealand flora, and has no near-allied species.

The new Asplenium, A. tenuifolium, is also found growing in the Wairoa Gorge. It was originally discovered at Takaka (vide Trans. N.Z. Inst., vol. xxiii., p. 424).

Some very large manuka trees were also observed on Little Ben, from 2ft. to 3ft. in diameter, the finest I ever saw. I do not know if this is an unusual size.

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Art. XLI.—Bush Jottings: No. 2 (Botanical).

[Read before the Hawke's Bay Philosophical Institute, 12th September, 1892.]

The harvest of a quiet eye.

That broods and sleeps on his own heart.

Wordsworth.

Having been called on by our Honorary Secretary to furnish a paper (or a “forfeit”*) for our branch Institute for this session of 1892, and having again spent a large portion of this year in this high inland wooded district (commonly called “the bush”), I think I cannot do better than to jot down a few of the more interesting botanical sights I have witnessed with more or less of delight, especially when considered in connection with the many pleasurable feelings they evoked. And these I would divide into three groups,—

I. Curious, scarce, and unique.

II. Peculiar and pleasing.

III. Striking, though common.

I. Curious, Scarce, and Unique.

1. And first of a fern, Polypodium pennigerum, Forst. While walking in a wood near Dannevirke, I was suddenly surprised on noticing a tall subarborescent fern of this species; its main caudex or stem was about 12in. high, rather slender, with six regular branch-stems (one of them being forked) issuing from around it, each about 1ft. long, and all upright, presenting a neat candelabrum-like appearance. Unfortunately the upper leafy portions of their fronds had been either cut off or eaten by cattle, leaving only their stems (stipites). These, with the branches and upper part of the main stem, were all lately dead, but the plant was springing vigorously afresh from near its base. Very likely, had the plant been uninjured and flourishing, with its large and numerous leafy and drooping fronds (in its usual state), I should not have seen its peculiar manner of growth, as it grew in a flat part of the forest. I had not unfrequently noticed this fern, when growing undisturbed on low alluvial ground by the sides of streams, to possess a short coalescent trunk of a foot or more long, but never before saw one branched; and so I thought it worthy of being recorded.

[Footnote] * This refers to a sentence in my Presidential Address of 1888—viz., “that every member should contribute annually at least one original paper, or five good specimens to the Museum, or two suitable books to the Library” (p. 19).

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2. Of an orchid, Gastrodia leucopetala, Col. In another part of the same wood I was much pleased on finding no less than eleven specimens of this (now rare) terrestrial orchid, all growing together within a small semi-enclosed spot of about 2ft. in diameter; and just beyond were two more. This was at the end of January, and of course they were all past flowering, as this curious plant flowers about Christmas; their upright reed-like stems were nearly alike in size, each being about 2½ft. high, and full-flowered. The eleven specimens were growing close to the base of a large living rimu tree (Dacrydium cupressinum), and nearly surrounded by its high and naked roots, projecting like ridges from its trunk, which no doubt had been the means of preserving the roots of these plants, which are tolerably large and fleshy, and are edible both by man (the old Maoris) and pigs. In fact, I have long been of opinion that the main cause of this orchid now being so rarely met with in its forest habitat is owing to its root being eagerly sought after and eaten by the wild pigs. For a full description of this fine species see Transactions N.Z. Institute, vol. xviii., p. 268. I may further remark that those specimens there described were also obtained from another part of this same wood.

While mentioning a species of the order Orchideœ, I may further observe that several of the indigenous epiphytal ones are well represented in the forests here—viz., Dendrobium lessonii, Col.; Earina autumnalis, Hook.; E. mucronata, Lindl.; E. quadrilobata, Col.; E. alba, Col.; also, but more sparingly, that curious and rare one Sarcochilus breviscapa, Col.: all these usually grow high up on the larger timber-trees, in the forks of their main upper branches, which makes it to be so difficult to get good specimens of them; but now that those trees are being felled for timber, specimens of those orchids are more easily obtainable.

These plants certainly add largely to the beauty of our New Zealand forests in their flowering-season, about midsummer, when gracefully pendent producing their numerous flowers at the tips of their long lithe branchlets swinging in the wind. Indeed, the curiously-marked long woody polished ringed stems of the Dendrobium are a pleasant object of contemplation and study, as such are sure to remind the beholder of the regularly-ringed and shining stems of the malacca and other walking-canes.

3. A fungus, Ileodictyon cibarium, Tulasne, var. giganteum, Col. Of this highly-curious fungus I have met with a remarkable fine specimen, which I have (for the present) termed a variety, but which may prove to be another species of that strange and singular genus. It is not only twice or three times the size of the largest I have ever yet seen, but it

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has other peculiarities. Unfortunately, the description of I. cibarium in Hooker's “Flora of New Zealand” is very insufficient. This species is pure-white, of an oblong shape, somewhat resembling that of a large inflated bladder of open network, being 14in. long and 9in. wide, possessing twenty-two large pentangular irregular-size meshes, the largest being about 4in. by 2in.; their ribs very wide, 6–8 lines, and much corrugated and pitted, with peculiar triangular holes in the middle of the rib at each outer angle: its volva, originally before bursting about the size of a pigeon's egg, is thickish, gelatinous, and strongly marked internally with white cross-lines corresponding with the more prominent net-like ribs of the pileus when closely compressed within.

But its curious history has yet to be told. It was late in the autumn (May), when I was in a grassy spot on the confines of a small retired wood (whither I had often been in former years), when on seating myself on a dead prostrate tree I noticed two or three common specimens of I. cibarium showing themselves among the low herbage; I collected them. On looking more closely I saw an olive-coloured egg-shaped fungoid substance peering up from the ground underneath a thick branch of the tree on which I was sitting, apparently as if it were pressed down by the branch. I broke the branch off carefully, when the egg-like substance rapidly burst open, and up sprang this fine specimen as if forcibly ejected by a spring, unfolding itself immediately to its full size. Its sudden and unexpected movement startled me; but after admiring this wondrous production of Nature, and its astonishing internal powers,—seeing, too, it was but a weak and flimsy tender substance without nerves,—I brought it carefully away in my handkerchief, and, after washing it with a feather in repeated waters (to remove its copious brownish slime of a most disagreeable odour, which is common to them all, including the closely-allied and handsome genus Aseroe), I dried it, and its volva or case, as a good specimen.

In former years (in the forties), before the introduction of cattle, specimens of I. cibarium were not unfrequently to be met with in open fern-lands, and generally fully expanded, usually from 3in. to 4in. diameter, and nearly globular; but I never before witnessed the bursting of a volva. The apparent strength, or power, shown by this small, soft, and tender fungus reminded me strongly of what we have read as recorded of some of the mushroom-like genus (Agaricus) in their displacing and forcing up the flat stones in city pavements.

As before stated by me in former papers read here, these fungi while in their young, unbroken egg-like condition were formerly eaten by the Maoris; in that state they have none of that offensive ill-odour that pertains only to the fully-expanded

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pileus, and which is confined to the thick brownish slime with which it is covered: the difference is just that between a fresh-laid and an addled egg.

4. Gentiana montana, Forst. Another plant which I think should be included in this group as being both very rare and strange in this low wooded district is a species of Gentiana, and, as I believe, G. montana.

The natural home of this pretty little flowering-plant is on the open grassy tops of the neighbouring high Ruahine mountain-range, where it embellishes the small herbage of its sub-alpine locality with its numerous pale and neat flowers, which are large for such a small plant. I have only met with it in one small open spot on Tahoraiti Plain, where several plants of it grew; but I do not think it is to be found anywhere else in all the lower and wooded grounds. My detecting it there very much surprised me; indeed, as it was so long back since I last saw it growing on the mountains (in 1852), at first sight I supposed it to be a new species. Now, seeing that the seeds of the Gentiana are neither minute nor light (feathery), the question arises, How should it be found here on the plains so far away from its natural mountain-home?

5. Another fern, Lomaria elongata, Blume (L. colensoi, Hook.; L. heterophylla, Col.). The same reason which led me to bring forward the preceding plant causes me also to note here this fine and peculiar fern. Its original habitat, where I first detected it (in 1842), was on the banks of a brawling mountain-stream in the deep forests in the interior to the north-west of Lake Waikare, in the celebrated Urewera country, where, on those alluvial flats, it formed large and continuous strange-looking beds, through which it was difficult to force one's way, there being no path or track: this, however, was partly owing to the small driftwood and trees carried thither by heavy floods being concealed among its thickly-growing large fronds, so that one stumbled at every step, often getting ugly and painful knocks on one's shins. And here I may remark that, in travelling in those early times, and always on foot, in those places along the sides of streams in the wooded interior, the plan was to cross and recross the stream continually to the more open bank, there being no track whatever, the only guide for direction of one's course being the stream itself.

Here, however, in this Hawke's Bay bush district, I only know of one small isolated spot on the side of a mountain streamlet where it is found, and it grows there luxuriantly. I have never before met with it save in the interior. A few years ago, however, a settler at Woodville (an old Hawke's Bay resident), in clearing his section of land, found this fern there growing, and, being much surprised on seeing it, from its

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novelty and size, and thinking it was new, sent me a specimen. It is a very striking fern, both from its large size and its strange appearance, and its equally curious manner of growth or disparity of form; and that not merely from its great difference in the barren and the fertile fronds (as obtains in other species of the Lomaria genus), but in its barren fronds, for, while its large fronds are usually very broad and coarsely pinnatifid, some of them are merely narrow, oblong, and simple (in this diform respect not unlike large specimens of Polypodium billardieri).

For my part, having given this fern much study, I am not inclined to believe it to be identical with L. elongata, Blume (a Javanese and Indian fern), as that species is largely drawn and fully described by Beddome in his “Ferns of Southern India.” Sir W. J. Hooker, on my sending him specimens of this New Zealand fern, and finding I had published it with a description in the “Tasmanian Journal of Natural Science,” in 1844, as L. heterophylla, immediately republished it with good drawings in his “Icones Plantarum,” naming it L. colensoi, there being already a L. heterophylla described at Home, but unknown to me here in New Zealand.

II. Peculiar and Pleasing.

In this group I would place a few of our local ferns and some other plants, but only such as are not commonly met with, and, when found growing in undisturbed spots, serve to entrance the beholder, rivet his attention, and fill him with admiration—that is, if he possesses an eye to see, and a mind to understand. I will begin with that newly-detected neat little maidenhair, Adiantum polymorphum, Col.,* which, since I first made its acquaintance in 1887, I have found in three different secluded spots in these umbrageous forests, and in each place forming small continuous and closely-growing beds, flourishing beautifully, and presenting a delightful appearance, from their elegant form, graceful drooping habit, and uniformity of colour and of cutting, which is further increased on gathering a specimen and noticing more closely its slender glossy ebon stems.

Two other species of this genus—A. hispidulum, Sw., and A. fulvum, Raoul—I have also noticed in forests at the North (Bay of Islands), possessing a similar habit, growing closely in beds forming large patches, like this species; but those are much larger and coarser ferns, though fine specimens of A. hispidulum are very handsome.

Here I will briefly mention another newly-discovered and very fine fern (some specimens are truly beautiful), Pteris

[Footnote] * Trans. N.Z. Inst., vol. xx., p. 215.

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(Litobrochia) pendula, Col.,* and this I also notice because I have detected it in two other localities in this neighbourhood, but, as before (originally), hanging thickly down from shaded cliffy spots, sides of streamlets difficult of access. Some of the plants were very fine, of most luxurious growth, and looking tempting, so healthy and charming.

In three dry spots in particular, far apart from each other, in the deep forests between Dannevirke and the River Manawatu, I have often gazed with delight on thick-growing patches or beds of that extremely neat and graceful tender fern Asplenium flabellifolium, Cav., one of the most elegant of its genus. This wood variety (as I deem it) has much smaller pinnæ than this fern commonly has when growing in open places, and they are more finely and sharply cut, and its narrow linear fronds, being also much longer, give it a still more graceful appearance; its colour, too, is that of a most refreshing light emerald-green. All this, however, may naturally arise from its moist shady home in the forests. It forms compact and healthy beds by overlying itself considerably (stratum super stratum), the long and delicate fronds emitting at their extreme circinnate tips minute rootlets, which adhere to the soil when they touch it, when they again send out fresh stems, and so form new plants. This fern, however, is well known among us, and that deservedly, from its beauty as a living fern - decoration when suspended in a light wire basket, as well as from its being so easy of culture; and therefore I should not care to mention it here were it not that it is rapidly becoming very scarce, and those three spots in the dry and ancient woods were so exceedingly lovely that they have left their natural and truthful images deeply impressed on my mind; so true it is, “A thing of beauty is a joy for ever.”

Having briefly noticed some of our smaller handsome local and rarer ferns, I will now say a few words respecting the bigger ones—the giants of the fern order—although many of them are generally very commonly distributed throughout the colony, and more particularly in the wooded districts.

Come on then, my hearers! Come with me into a secluded calm and quiet dell, in a deep-shaded forest, far away from the haunts of man! Let us go to a sacred spot well known to me, and still remaining free from the incursions of the ruthless invader, both quadruped and biped! May such concealment long continue!

Here, at the level bottom of this dell, down whose stony sides we have been scrambling, through which a small purling streamlet of clear water winds its tortuous way, stand a

[Footnote] * Trans. N.Z. Inst., vol. xx., p. 218.

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group of majestic-looking tree-ferns, species of Dicksonia; they are about, say, 20ft.–25ft. high, and stand pretty far apart from each other, so that one can walk easily between them, and sit down, if so disposed, on the low and soft grassy herbage at their bases. Above, at top, their perennial crowns of large spreading green fronds extend, meeting and crossing each other—some horizontally, some gracefully drooping—while their stout upright stems are thickly clothed with their own dead and grey-brown fronds, hanging closely and not ungracefully down, wrapping them, as it were, in tolerably regular rows or layers from the base to the top, as if to protect their trunks, or even to keep them warm. Those dead hanging fronds are from their natural and regular yearly decay, and evidently not a single frond has ever fallen off or been displaced. They greatly add to the solemn and still beauty of the scene. If gently lifted their clean stems will be seen in all their rich brown colour and fibrous comeliness, without any small ferns, mosses, or other plants growing on them.

Such a spectacle, when undisturbed and deeply embowered and surrounded by ancient timber-trees,—

Those green-robed senators of mighty woods,
Tall oaks, branch-charmed by the earnest stars,
Dream, and so dream all night without a stir.

Keats, “Hyperion.”

—is to me a most pleasing one, causing me to behold it with bated breath, with a kind of feeling approaching to sentimental awe, better felt than expressed in those deep secluded forests—such a feeling as one might reasonably suppose would arise within the bosom of the wary and discreet visitor to the ancient oracle of Apollo at Delphos three thousand years ago. In such a place, and with such feelings in this retired solitude in the grand temple of Nature, the suitable words of Bishop Heber, so descriptive of “majestic silence,” are likely to be vividly recalled to mind,—

No hammers fell, no ponderous axes rung;
Like some tall palm the mystic fabric sprung.
Majestic silence!

*

Heber, “Palestine.”

But there is yet another and a very different sight to be seen and admired among my groups of big living tree-ferns—

[Footnote] * This quotation from Bishop Heber's poem was altered in later editions to—

No workman steel, no ponderous axes rung,
Like some tall palm the noiseless fabric sprung.
Silently as a dream the fabric rose,
No sound of hammer or of saw was there.

[Footnote] I may here observe that these two last lines are also in Cowper's “Task,” the Winter Morning Walk, book v.

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one sure to evoke feelings of an opposite character in the bosom of the beholder, for, if the former were of the “Penseroso” class, these would as surely pertain to the converse or the “Allegro” one.

Here, then, in another umbrageous solitude, is a similar lot or small natural secluded grove of tall tree-ferns, generally of the genus Cyathea; but their stout stems are entirely without that solemn-looking dead grey-brown wrapping, and, instead, they possess a most beautiful and elegant closely-compacted light-green and glossy dress, composed of very small living creeping ferns, pendulous and thickly imbricated like tiles on the roof of a house, often delightfully glistening when visited by a passing ray of sunshine. These small ferns are mostly composed of two species only—Trichomanes venosum, Br., and Hymenophyllum flabellatum, Labill.—and they do dwell together apparently in the most pleasing harmony, as if enjoying life. They often completely enwrap the whole large and tall trunk of the tree-fern from base to apex, all green and flourishing, without showing the smallest spot of intervening open space, evidently the perennial and steady growth of many years. These little ferns are something more than of epiphytal development, pertaining rather to that of quasi-parasitical, for their creeping rhizomes and roots penetrate deeply into or among the outer dead matted stipites and fibres of the tree-ferns on which they flourish.

Perhaps I had better end here respecting the tree-ferns. But then you, my audience, “dwellers at home at ease,” would only know half,—and that of my woodland joys: so it is but fair you should also know a little of my sorrows, otherwise you would remain in happy ignorance of them. These, however, I shall only briefly touch on, owing to the extreme disagreeableness of the theme.

And first of my majestic venerable-looking group. On my return on one occasion to one of those dear old haunts, I found, to my horror, that some Goth or churl had recently been there, and had set fire, separately, to each one of those eight or ten big tree-ferns! just to burn off their thick dry wrappings, the undisturbed growth of many years, and so to make a blaze; and there their blackened and half-charred stems stood, with their once lovely elastic crowns of fronds sadly scorched and stiffened above them—a piteous sight! I could fancy they even reproved me, and I could have wept.

I had long had good reasons for believing that my visits to that unfrequented part of that old forest, so difficult of access, were watched by one or more of the underlings or stockmen of the neighbouring sheep-station, who, I suppose, on his going thither after me, and not discovering what it was that could have induced me so frequently to visit that place (for the old

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belief was that in such spots I was fossicking for gold), vented his disappointment in that way—by striking a match or matches and setting fire to those tree-ferns out of mere wantonness. Several such instances had occurred in former years during my sojournings at Norsewood, some of them having been caused by so-called “picnic” parties, and some by teetotallers—judging from the labels on the bottles left behind!

Before, however, that I quit this pre-eminently pleasing and loved subject of our New Zealand ferns, I would call your attention, and especially that of the young-lady portion of my audience, to an interesting, novel, and elegant sight I have several times seen and admired while residing in the bush; this, too, being an artificial and neat method of preserving them. To me, indeed, it was unique, never having before noticed anything of the kind.

A bunch or small bundle (I might almost term it a bouquet-de-plumes) of an assorted few of our larger ferns—viz., Polypodium pennigerum, Lomuria fluviatilis, Asplenium lucidum, Adiantum cunninghamii (the handsome species of maidenhair), Hymenophyllum dilatatum and H. demissum, and Pteris (Litobrochia) pendula (my new fern)—were loosely bound together much after the fashion of a sheaf of wheat, with the tips of the longer specimens gracefully drooping, and placed so as to stand erect on a black stand under a tall cylindrical glass with closed dome-shaped top. These were all perfect, pure-white—dead or frosted white like silver or tissue-paper, with every tiny leaflet fully expanded, and with the veins and seed-receptacles and capsules clearly and beautifully shown. The leaves, moreover, of some of them are thickish and obscure in their living state (as of Asplenium lucidum), but now they were equally thin and semi-transparent like those of the others.

I saw this elegant and peculiar specimen of art-decoration—so chaste and simple and yet so strikingly lovely—at the Club Hotel, in Woodville, in the larger parlour upstairs; I often admired it. There it stood, conspicuous among other ornaments, on the top of a high dark-coloured piano. I do not know how the remarkable change, which seems to be permanent, was effected; I made inquiries of the proprietor, but he being newly entered did not know. I am aware that very great alteration can be caused by bleaching vegetable fabrics with the fumes of burning sulphur, and this may have been so effected. Be that as it may, it seemed to me to be a new and easy mode of admirably and more completely displaying the hidden natural beauties of our lovely New Zealand ferns, and so I bring it to your notice.

One other little-known plant must, not be omitted from

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this list—namely, Metrosideros tenuifolia, Col.,* and this from its very peculiar manner of growth, its pleasing colour, and its strange homes. I only first detected this plant about a year ago, and then (like many others) it was confined to one spot, where, however, it grew abundantly. Since then I have noticed it growing in several places, but all similar—that is, on the sides of steep cliffs, all the better if somewhat concave. In such spots it revels, repeatedly overrunning itself, flourishing luxuriantly. It adheres very closely to the soil, like small-leaved ivy, in England, to trees. The great regularity of its little round and glossy leaves, and its numerous slender red branchlets, afford a charming picture. What an elegant plant for rock-work, and for a permanent stone or clay alcove or bower! But words fail to describe this lowly-living ever-green beauty.

There are yet some other peculiar plants, which, though small singly in themselves, and of no striking beauty to arrest the eye of the beholder, should not be overlooked, as they often impart, from their curious appearance and situation on the dead and dry overhanging branches of trees, additional solemnity to the shaded and secluded woodland scenery.

Of these are some of our larger and foliaceous tree-lichens, such as several species of the genus Sticta, viz.: S. fossulata, Dufour; S. freycinetii, Delise; S. argyracea and S. carpoloma, Delise; and Usnea barbata, Fries (“old-man's beard”), several varieties.

It is well known that lichens live to a very great age; they retain their vegetative and productive powers uninjured throughout the hottest and driest seasons on the highest and most exposed dead branches: although, on gathering them at such times, they crumble to fine powder in the act, yet, on their becoming wetted from rain or dew, they are soft and flaccid, and may be folded up without breakage or injury.

I have seen very large specimens of the above-mentioned lichens, some specimens of the Usnea (fitly termed “old-man's beard,” being thread-like, bushy, and pendent), 1ft.–2ft. long; and some specimens of Sticta extending from 1ft. to 18in. in diameter, and very fully and complexedly branched, their branches flat and bearing much fruit, which is often curiously and regularly placed like little shields or saucers on their margins.

They are all very numerous, and grow to perfection in damp gullies, especially on overhanging trees and shrubs in their sides in sheltered declivities; and often, when they are of a large size, and sombre lurid leathery appearance, hanging from the bare and dead branches, they give an uncanny,

[Footnote] * Trans. N.Z. Inst., vol. xxiv., p. 387.

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weird-like aspect to the solitary scene. At such times, pictures from Goethe's “Faust”—particularly of Faustus and Mephistopheles ascending through the dry mountain-woods to the witches meeting on the Brocken—have been forcibly called to my mind, and I have thought how such pictures might be further improved by the addition of some of those large, flapping, strange-looking lichens to the naked and dead branches of those gnarled mountain-trees, even more so than by the artist's introduction of flitting bats into such a scene, as bats do not fly by night.

Furthermore, in those dry and stony hill-sides, when the soughing winds sweep fitfully over the arid barren plains around and above, and blow among the stiff and hardened thin-edged lichens hanging from their denuded branches, not unfrequently sharpish, shrilly, stridulous, and low wailing sounds are heard, which are not, however, unpleasant, and serve to increase one's strange thoughts and mournful feelings, especially if alone—much as Wordsworth has it,—

In that sweet mood when pleasant thoughts
Bring sad thoughts to the mind.

III. Striking, though Common.

A few plants that are very frequent on the sides of the railway-line between Dannevirke and Woodville, and almost sure to arrest the eyes of some of the passengers, from the oddness and singularity of their appearance, may here be briefly mentioned, and that because very often certain questions are sure to be asked concerning them, especially at this, the winter-cum-spring season of the year.

And first I would take two that are often seen growing together close to the railway-lines, upright, single-stemmed, and pretty nearly of the same height (3ft.–6ft. or so), one a small young tree-fern (probably a Dicksonia or a Cyathea), and the other a young “cabbage-tree” of the settlers (Cordyline australis). These, with all the herbage and small ever-green shrubs that grow thickly around them, have been lately set on fire (I suppose, to clear the sides of the railway-line); and while the herbage and shrubs have been thus destroyed—burnt up—these two plants are still living, and fast shooting their large bright-green leaves and fronds from their tips and so forming living crowns, while their stems present a hideous black appearance, as if not only scorched but thoroughly burnt and killed, the whole of their bark and outer woody layers having been destroyed; increased, if possible, by the great contrast in colours, shown in their long dry and pale faded leaves hanging irregularly down from their tops; these leaves having been scorched and killed by the fire, but being thick and green were not completely burnt up. And the question

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is almost sure to arise from some one observant person in the carriage, “Why is it so? Why are these two plants alone so salamander-like as to live through the terrible ordeal of raging fire?” And mark, this inquiry arises from only one, who may be laughed at for it by the company—the many,

With the loud laugh that spoke the vacant mind.

For to the many there is nothing to be seen, nothing to be noticed, nothing worthy of observation in the whole scenery through which we are passing on both sides, whether botanical in charming variety and profusion, or geological as revealed by the varied horizontal strata in the sides of the deep cuttings through which we frequently thread our way. Such unobservant travellers and tourists too often remind one of Words-worth's “Peter Bell”:—

A primrose by a river's brim
A yellow primrose was to him,
And it was nothing more.

Of course, the answer to that question is an easy one, though the cause may not be known to all: these two plants belong to the endogenous class, whose living woody system is internal and central, and not on the outside, under the external bark, like those others of the exogenous class around, that have at the same time been burnt and so perished. Large tree-ferns 20ft. to 25ft. high are frequently to be seen on the edge of or a little way within a burnt forest—that is, their blackened burnt stems standing like charred and sooty pillars, while from their tops large crowns of young bright-green fronds are springing and spreading, and so presenting a curious and strange contrast. At the same time, not a single tree or shrub of that forest has escaped the ravages of the fire; all besides is dreary desolation, vegetable death.

There is yet another plant that is very common in the woods near the railway-lines which, from the great singularity of its appearance, deserves notice. It grows only on the upper large branches of trees, where it forms round ragged bunches of rather long grass or leek-like leaves, and sometimes several of such bunches are together, forming quite a big mass. It shows itself more conspicuously and strangely when growing on dead burnt and still standing trees, which is very frequently the case, and has often astonished me from its tenacity of life. How those small and feeble and exposed plants escaped the fiery doom which destroyed the big and stout trees root and branch on which they are still living and flourishing is a mystery to me. Further, the bark of many of those burnt trees has peeled off, leaving only their pale, bleached, denuded limbs, on which those plants still adhere

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and grow and live, which serves to make their appearance the more singular.

This plant is a species of Astelia, and probably A. spicata, Col.,* which species, as far as I know, is confined to this wooded district. There are several species of this genus known to inhabit New Zealand, and some of them are of a very large size, especially in the northern woods, where, high up in the lofty trees, they resemble huge crows' nests.

And now, my audience, I have done. Believe me,—

There is a pleasure in the pathless woods;
There is a rapture on the lonely shore;
There is society where none intrudes,
By the deep Sea, and music in its roar:
I love not Man the less, but Nature more.

Byron, “Childe Harold.”

Art. XLII.—Cryptogams: A Description of a few Lately-discovered Rare Indigenous Ferns; also, Notice of a Fine and Peculiar Fungus, Ileodictyon, Tulasne, = Clathrus, Cooke.

[Read before the Hawke's Bay Philosophical Institute, 28th November, 1892.]

Order I. Filices.
Genus 11. Adiantum, Linn.

1. A. pullum, sp. nov.

Rhizome as stout as a goose-quill, creeping, densely hairy and scaly; hairs reddish-black; scales black, large, acuminate, glossy. Plant 6in.–8in. (sometimes 10in.–11in.) high, suberect and drooping, ovate and subpedate; several fronds springing close together from rhizome, 6–8 within lin.; stipes (and rhachises) very slender, almost filiform, black, glossy, mostly curved or irregular not straight, 4in.–5in. long, rarely 6in.–7in., channelled on upper surface, slightly scaly below and semi-muricatulate; frond 3in.–4in. (sometimes 5in.–5½in.) long, always more or less dark-coloured on both

[Footnote] * Trans. N.Z. Inst., vol. xiv., p. 335, for m., and vol. xv., p. 340, for f. plant.

[Footnote] † The numbers attached to orders and genera are those of them in “Handbook of the Flora of New Zealand.”

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surfaces, some pinnæ are nearly black, glaucescent below, usually bipinnate and tripinnate, generally 3 sometimes 4 rarely 5–6 branches long curved pinnate; pinnules alternate, rather distant, patent on long filiform petioles, mostly small, of various shapes and sizes on the same plant, broadly cuneate, parallelogrammiform, roundish-oblong, suborbicular and subrhomboid, 2–3 lines long rarely 4–5, gradually decreasing in size to tips, the upper pinnules close and very small, the ultimate one rhomboidal obtuse; the lower margin (or sometimes 2 margins) being the continuation of petiole always thickened straight even glossy and coloured; the upper margins cartilaginous laciniate and serrate, teeth large white hard and sharp; veins numerous, close, free, much dichotomously and flabellately branched, several pairs rising and spreading from a single basal vein, and all subradiating from the petiole or lower basal angle. Sori few but of a large size and very prominent far beyond margin of involucre, on the lobules and not in the notches of the pinnules. Involucres brown shining (black in age), rather large, their margins gaping elevated, generally 5–7, sometimes 9, on the larger pinnules, on the upper margin and partly extending round the outer or tip; smaller and very close together on the small, and only 1, 2, or 3 on the smallest pinnules; sinus deep; when young, however, they are very thin white and crisp, or crumpled.

Hab. Open land, damp shaded spots rocky places, between Dannevirke and the East Coast, County of Waipawa; 1892: Mr. H. Hill.

Obs. I. This fern has given me much extra labour, from its possessing some of the common characters of A. cunninghamii, Hook. (A. affine of some modern writers on ferns; but quœ.), and of other allied species (particularly A. heterophyllum, Col., Trans. N.Z. Inst., vol. xx., p. 218); but (as I fortunately possess a large number of specimens of all sizes, through the liberality of its kind discoverer) I believe it to be very distinct as a species. Those “common characters” pertain more or less to all that sub-family of Adiantum, most of the species also being exotic. Of this fern, its manner of growth, its black filiform stipes (indeed, the almost general blackish colour of the whole plant), its large black and shining scales, its small and variously-shaped pinnules, and, above all, their laciniate and sharply serrate margins, with compound and radiating veins and venules, afford good and constant characters.

II. I have not infrequently met with, and possess, dwarf specimens of A. cunninghamii (some being little pigmies), as well as extra-large ones, but these do not contain the peculiar and distinctive characters of this fern.

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Genus 13. Cheilanthes, Swartz.

1. C. venosa, sp. nov.

Plant slightly tufted. Stipe suberect and curved, 3in.–3½in. long, very slender almost filiform, terete, lightly furrowed on upper surface near base, glabrous, light-red and glossy (as, also, rhachis and subrhachises), with a few small weak scales scattered throughout. Frond 2in.–3in. long, sub-deltoid-ovate, 1½in.–in. wide at base, apical lobe very large (for plant), deeply incised obtuse; bipinnate light-green, glabrous, with a few distant scattered fine weak and rather long white hairs on both surfaces; pinnæ 4–5 jugæ; 3 lower pairs opposite, distant ¾in.–1in. on rhachis, sub-deltoid-ovate, 1in.–1½in. long, about 1in. wide at base, petiolate; uppermost pairs subsessile and pinnatifid; pinnules ovate, obtuse, pinnatifid, deeply incised, lobed; lobes oblong; tips of lobes and lobules irregularly bluntly toothed, much veined; veins pinnate, free, regularly branching from midrib, largely dichotomous, each lobe and lobule containing many straight venules and veinlets, extending to margin. Sori loosely scattered, generally on tips of pinnæ and of lobes in irregular little batches, mostly very small, sometimes mere dots. Involucre green from the incurved margin of frond, small and (sometimes) 1–2–3-cleft and toothed, rarely covering sori.

Hab. Dry hills, among low shrubs and undisturbed indigenous herbage, in various localities in the County of Hawke's Bay; rather rare, nowhere common.

Obs. I. This is a very neat little fern; its fresh and charming green colour alike on both sides (which it also retains in drying), and its light-red glossy filiform stipe and rhachises, give it an elegant appearance, which is also increased on examination and observing the curious disposition of its sori and involucres, and its remarkably regular and curved numerous venation.

II. I have known this fern for a considerable time, but only during this year (1892) have I succeeded in obtaining really good specimens. I think its fronds are annual or biennial. Old states, more or less dried up, are difficult to examine closely and satisfactorily, and much resemble those of C. tenuifolia, Swartz, to which species (and also to C. sieberi, Kunze) it is pretty closely allied. But from C. tenuifolia it differs in several particulars (vide descript.), and most especially in its peculiar and striking venation, which does not vary, and forms a good specific character. Sir W. J. Hooker has given a drawing with dissections of C. tenuifolia (likewise of C. sieberi) in his “Species Filicum,” of which he also says, in his description of that fern, “Our figure will give a better idea of the plant than whole pages of description can do”

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(l.c., vol. ii., p. 83): there the venation of the pinnules is shown as extremely simple and distant and not extending to margins. And just so it also is shown in the larger drawings with dissections of C. tenuifolia given by Beddome in his “Ferns of Southern India,” plate 188 (also referred to by Baker in his description of that fern in his “Synopsis Filicum”). There the veins in the lobes are simple and common, showing the midrib from the rhachis with 3–4 single veins on each side that do not reach the margin in each lobule; also the involucre continuously extending over 3 lateral and 4 apical veins, with its margin even. Moreover, C. tenuifolia is shown to be a much larger and coarser fern, tripinnate with 5–6 pairs of pinnæ, its lower pinnæ compound (or tripinnate) with longer petioles, their tips, with that also of the frond, being subacute; and in his description of this fern he also says, “Stipe and rhachis purple-black; the main rhachis is winged above, and the secondary and tertiary rhachises are all narrow-winged” (l.c., p. 64); and Sir W. J. Hooker says the same in “Species Filicum,” p. 82—characters that are not found in this fern, C. venosa.

Genus 16. Lomaria, Willdenow.

1. L. pygmœa, sp. nov.

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

Plant very small, tufted, 2in.–3in. high; subcaudex an erect thick bunch of old stipites ¾in.–1in. long, with numerous long black scales, acuminate, acute, glossy; roots long, spreading, terete, glabrous. Barren frond spreading linear-lanceolate, 1½in.–2½in. long, 2–3 lines wide at middle, pinnatifid, sub-membranous, pea-green, glabrous, glossy above, rhachis channelled; pinnules 13–15 on each side, alternate, regular, semi-orbicular or hippocrepiform, very small at base, apical lobe subacute with pinnate veins; margins slightly uneven, sub-cartilaginous, whitish; veins few, 3–4 pair in each pinnule, simple and forked, extending to margin, tips clavate; stipe slender, short, sub ½in. long. Fertile frond shorter, suberect, very slender and narrow, linear, 2in. long, 1/10;in. wide, pinnate; pinnæ alternate, orbicular, about ½ line diameter, sessile, about 13 pinnæ on each side of rhachis, the lower and middle ones distant, the lower most minute, apical lobe 4 lines long. Sori numerous, spreading, close, compacted, covering pinna, dark-brown. Involucre narrow, dark - coloured, reverted, margins entire.

Hab. Open lands, damp spots rocky places, between Dannevirke and the East Coast, County of Waipawa; 1892: Mr. H. Hill.

Obs. A peculiar little species: its very small size, venation, and minute orbicular fertile pinnæ distinguish it readily from all others of the genus.

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2. L. procera, var. gracilis, Col.

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

Plant tufted, erect, very slender; roots numerous, bushy, densely and finely hairy; hairs red. Barren fronds suberect and drooping, 9 in number from 1 rootstock, of various lengths, 4in.–8in. long, 1 ½in.–2in. wide, linear-lanceolate, pinnate; stipe 2in., almost filiform, pale-reddish, dry, sulcate above, very slightly scaly; pinnæ very thin, pale-green, alternate, few, 7 on each side of rhachis in longest specimen and 4 on short ones, sub-linear-elliptic, the longest 1in. long and 4 lines wide, patent and slightly falcate, subacute and obtuse, midrib very narrow, deeply channelled above with raised edges, margins sharply serrulate the teeth curved upwards and long, and close at tips, dimidiate, base truncate, the upper half more so, petiolate, petioles short very slender, ¾in.–1in. distant on rhachis, upper pinnæ subsessile, acute, the lower half decurrent, apical lobe linear-ovate acuminate, 1½in. long, the lowermost pinnæ very small, suborbicular, 3–4 lines diameter; veins simple, rarely forked. Fertile frond erect, pinnate, 10in. long, 2½in. wide; stipe 6in., much stouter than in the barren fronds but not 1 line wide, red, glabrous; pinnæ alternate distant, 6 on each side of rhachis, very narrow-linear, 1in. long, 1/10;in. wide, sessile and decurrent, the lower pinnæ 1½in. distant on rhachis, the upper 3 pairs closer, apical lobe 1½in. long, the lower fruiting pair of pinnæ subsessile, and the lowermost pair of pinnæ barren very small 4 lines long broadly ovate tips rounded. Sori numerous, compact, dark-brown, not extending to tips of pinnæ, which are leafy 1–2 lines long, and so also the lower fruiting pair at their bases. Involucre dark-brown, subinvolute and adhering, very finely fringed throughout.

Hab. Open margin of low wood, edge of great plain south of Dannevirke, County of Waipawa; 1892; scarce: W.C.

Obs. I again visited that spot with difficulty, on recovering slowly from illness, in the autumn of 1892, and managed to bring away one entire and perfect plant, which looked surpassingly graceful in its sheltered home; and, although primâ facie it seems so very different from all the (known) varieties of L. procera, yet, on careful examination and comparison, I am obliged to consider it to be but another variety of that variable species.* Its striking points of difference are—its slender, graceful, and neat appearance; its few, thin, small, distant, obtuse pinnæ, with their finely-serrulate margins; its filiform and long stipes; and its densely-hairy and red roots.

[Footnote] * Sir J. D. Hooker, in his “Handbook of New Zealand Flora,” (published thirty years ago), gives four varieties, of which he says, “The varieties enumerated keep their characters under cultivation.” Some of them both Cunningham and myself had considered to be good and valid species, and to that number others have been added since.

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Order VIII. Fungi.
Genus 24. Ileodictyon, Tulasne.

1. I. (Clathrus) giganteum; Col.

Receptacle pyriform, 14in. long, 9in. wide, white; interstices very large (some 4in. by 2in.), pentangular; ribs 6–8 lines wide, much and finely crumpled, with small triangular apertures in the middle of the rib at each outer angle. Volva ovoid, white, thick, skinny, gelatinous within, with long white rootlets.

Hab. On ground, edge of forest south of Dannevirke; 1892: W. C.

Obs. I. For a more particular account of this fine and highly curious fungus, including its peculiar manner of unfolding from its volva, see my paper, “Bush Jottings” (supra, Art. XLI.).

II. Since writing that paper I have received a copy of Dr. Cooke's “Handbook Australian Fungi” (lately published), and I find that he has removed I. cibarium, our more common New Zealand species, into the allied old Linnean genus of Clathrus; and also given a drawing of I. cibarium, with its description (loc. cit., p. 215), and this serves to settle my doubt as to the validity of this species.

Art. XLIII.—Phænogams: A Description of some Newly-discovered Indigenous Plants; being a Further Contribution towards the making known the Botany of New Zealand.

[Read before the Hawke's Bay Philosophical Institute, 28th November, 1892.]

Class I. Dicotyledons.

Order I. Ranunculaceæ.
Genus 3.* Ranunculus, Linn.

1. R. sychnopetala, sp. nov.

Plant large, tufted; radical leaf suborbicular, 3in. long, 3⅓in. wide, apex slightly produced rounded and subtrilobed, base truncate and in a small degree turned up over lamina close to petiole, thickish, soft, upper surface green slightly hairy, the under-surface paler and more hairy; hairs weak

[Footnote] * The numbers of the orders and genera given here are those of them in the “Handbook of the New Zealand Flora.”

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wavy reddish, thicker longer and subciliate at margins; 9–10-veined; veins pale, sunk in the upper surface, slightly conspicuous beneath; veinlets closely anastomosing, forming long narrow angular areoles; margins coarsely and irregularly crenate-serrate; petiole 1¾in. long, 2 lines wide, stoutish, brown, hairy; hairs long appressed strigillose reddish; stipules at base small narrow. Flowering-stems 9in. high, solid, stout below nearly ¼in. diameter, two springing together from a single basal leaf; leaf subovate acuminate, stout, lamina 3½in. long 1¼in. wide many-nerved (9); veinlets anastomosing; tip very obtuse; lateral margins coarsely serrate with 6–7 broad teeth, gradually tapering to base; petiole 1in. long, very broad flattish and thick, nerves continued down petiole; small stipules at base; each flower-stem trichotomous 4in. from base, surrounded by a pair of bract-like sessile oblong leaves 1½in. long; pedicels 1-flowered, stout, sub 6in. long, with (in one specimen) a whorl of three leafy bracts about the middle, subovate sessile, irregular in size and in cutting, the largest having a pair of large lateral teeth almost trifid, the others entire, hairy, margins ciliate; hairs wavy reddish; and in the other specimen with a single trifid bract. Flowers: Calyx pale greenish-yellow; sepals 5, linear obovate, ½in. long, sub 2 lines wide, tip obtuse, concave, distant, hairy, margins ciliate, much veined; vein single at base, 5-branched at middle and united at top. Corolla pale-yellow glistening, 1in. diameter; petals numerous (40–45) in 3 rows, recurved, cuneate, 8 lines long 2½ lines wide, much veined, more so than sepal; tip rounded very obtuse entire; base tapering, claw long; gland small orbicular, about 1 line above base. Anthers numerous, stout, before bursting broadly elliptic, afterwards elongated and much narrower, deeply channelled on back, very glossy, same colour as petals; stamens broad flattish as wide as anthers, 2-nerved. Carpels 0, but instead a few small greenish petaloid leaves, much incurved and forming a small green ball.

Hab. Ruahine Mountain-range, east side, near summits of lateral spurs; 1891: Mr. A. Olsen, Norsewood.

Obs. Of this fine and very peculiar plant I have only received two flowering specimens, both, however, in good condition. At first I thought it to be a “monster” flower of R. insignis, Hook., or of R. ruahinicus, Col.; but after a very close and patient examination and comparison I find it to be distinct, though, from its not possessing any carpels, but numerous small petals in their place, it may prove to be a “monster” (or double) flower.

2. R. longipetiolatus, sp. nov.

Plant erect, glabrous, stolons few, short. Roots numerous long wiry very slender; sometimes rooting at lower nodes of

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flowering-stem. Leaves few, single, on tops of long petioles, spreading, in circumscription subreniform and narrow hemispherical, 1½in.–2in. long, 2½in.–3in. broad, trifoliolate, each lobe largely petiolulate subflabelliform and broadly cuneate, trilobulate, sinuses deep obtuse and very wide, lateral margins always entire, lobules trifid (and variously lacimate), generally with 1 large central and 2 small teeth their tips obtuse; petiolules slender sometimes 1in. long, veined; lamina thin largely veined, with numerous compound anastomosing veinlets and venules; petioles fistular, 7in.–10in. long, stout when fresh, with a long narrow stipule at base. Flowers few small, single on long erect peduncles, some directly from the rootstock 9in. long, others (and generally 1–3) distant on flowering-stem, axillary from a single cauline leaf and twice the length of its long petiole—sometimes 4in. long, occasionally 2 flowers springing together axillary on separate pedicels. Sepals 5, much shorter than petals, concave, inflated, tawny, glabrescent, 2½ lines long, broadly-ovate or oblong-rounded, tips very obtuse, 3-nerved, nerves flexuous, margin very membranous, white, pellucid. Petals 6, flat, narrow linear-spathulate, 4½ lines long, sub 1 line wide, tips obtuse and emarginate, tapering to base, pale-yellow glabrous, 5-nerved; nerves straight branching above not extending to tip; gland near base small, reaching across petal, hollow, depressed. Stamens short, sub 24; anthers elliptic slightly subapiculate. Achenia orbicular, turgid, sub 1 line diameter, slightly rugulose-muricatulate; styles same length, curved, slightly puberulous; stigma capitate, subpenicillate. Receptacle small elongated oblong subclavate, coarsely hairy at base.

Hab. In watercourses, forests near South Norsewood, County of Waipawa; 1882: W. C.

Obs. This species is certainly near to R. macropus, Hook., but on a close examination and comparison there will be found several grave differential characters. Indeed, it was owing to my having supposed it to be that species, or a variety of it, that I have so long delayed describing it; and to this opinion I was in great measure led through merely reading the specific description of that species as given in the Handbook. Besides, I had intended to revisit Norsewood and to obtain more and fresh specimens—which also caused me to put it off—which I have never since done. Now, however, on referring to the full and particular specific description of R. macropus (the type specimens found by me at Poverty Bay in 1839), as originally given by Sir Joseph Hooker in the “Icones Plantarum,” accompanied by a drawing and dissections (vol. vii., tab. DCXXXIV.), the differences are plain and great, and clearly shown in the drawing. That species has much larger sepals than petals, which peculiar character also caused Sir Joseph

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Hooker there to observe, “A very remarkable plant … from the smallness of its petals as compared with the sepals.” Besides this there are several other differential characters in its leaves, flowers, and fruit.

Order VI. Caryophylleæ.

Genus Cerastium,* Linn.

1. C. truncatulum, sp. nov.

Plant annual, small, erect, 1in.–2in. high, simple, some-times slightly branched, very hairy; hairs patent not viscid. leaves, radical subrosulate linear-spathulate, smaller than those on stem; stem-leaves linear-oblong obtuse, 3–5 lines long, sessile, dark-green, margins purple, ciliate; hairs jointed, white. Flowers 2–4, axillary near top, and 1 terminal, rather large for plant, open, 2 springing on long pedicels from one of pair of opposite leaves, pedicel ½in. long, slender, bibracteate at middle. Calyx shorter than petals, 2½ lines long, lobes subacute, green, purple-tipped, with large white membranous margins. Petals longer than calyx, bifid half-way down, lobes acute; styles 5, long, hairy; capsule twice as long as calyx, stout, slightly curved, shining with 10 teeth; teeth short, very broad, tips truncate and notched. Seeds numerous, orbicular, muricated, ochraceous.

Hab. Open grassy plains south of Dannevirke, County of Waipawa; 1887–91: W. C.

Obs. I have long known this little plant, and have often slightly noticed it, supposing it to be an introduced British species (two or three of them being now common here, imported among grass- and clover-seeds), but during this spring (1891) I was led from its humble beauty to gather and closely examine it, and believe it to be a new and undescribed species, the teeth of its capsule being so very different from those of all other species known to me, and so affording a good differential character. The plant has some general resemblance to C. semidecandrum; it is an early spring flower.

Order XVIII. Rhamneæ.

Genus 1. Pomaderris, Labill.

1. P. mollis, sp. nov.

Shrub 9ft. high, upright handsome growth, branched from base; branchlets densely stellate pubescent, also petioles under-surface of leaves flowering-stems and calyx on outside. Leaves alternate distant softish, usually 1in.–2in. apart, ovate,

[Footnote] * This genus is not inserted in the “Handbook of the New Zealand Flora,” although those others very near it are—Stellaria, Spergularia, &c.

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3in.–4¼in. long, 1¾in.–2⅛in. wide, tip obtuse, base rounded; also, often irregular in size and shape, some being much smaller, 1in.–1½in. long, elliptic, tip much rounded, on same branchlet with the large ones and generally below them; margins denticulate sub-crenate-serrate, dark-green, deeply rugulose, glabrous and shining above with sunken nerves, pale dull-green and stellate-hairy below, the hairs white and regularly scattered (not crowded) on lamina, but reddish and densely close on midrib and veins; veins few, regular, much produced, diagonal, parallel 4 lines apart, their tips branched on the posterior side; petioles stout, soft, ¾in. long, terete, slightly sulcate on the upper surface, closely hairy. Flowers in large loose compound terminal (and subterminal) panicles, 5in.–6in. long, 7in.–8in. broad at base, subpanicles 4in.–5in. long, with a small leaf at base, their branches loose distant slender spreading. Flowers close, soft, subfascicled 3–6 together; pedicels about 1 line long; calyx pale-green, 1½ lines diameter, 5-parted, sepals ovate recurved, keeled above, densely stellate-hairy on outside, tube very short; petals 0; anthers subobovoid, obtuse, orange-coloured, filaments flattish erect a little longer than style; style stout furrowed, top 3-cleft one-third of its length; stigmas large, capitate, rough. Ovary hairy, with scattered adpressed stellate hairs and also other hairs simple erect acute as long as style. Capsule rounded, the exserted part as long as the adnate tube, dark-brown. Cocci whitish-brown, elliptic subapiculate, submembranous, convex keeled on inner face and opening by a basal slit extending half-way up, minutely puberulous.

Hab. Dry hills near Puketapu, west of Napier, Hawke's Bay; rare; 1890–92; flowering 10th November: W. C.

Obs. This shrub is certainly very near to P. tainui, Hector,* differing, however, in size of plant, form, &c., of leaf, and wanting its gland to anthers, &c.; and as I have already noticed and described how closely two (at least) of our northern species of this genus approach each other until they are fully examined, just so it may be with these two plants. At all events, if this plant should prove to be identical with that species, then another legendary Maori support and witness (!) of their wild, mythical canoe-arrival on these shores will again have to be abandoned—with regret, not only by themselves, but also by their European supporters.

[Footnote] * See Trans. N.Z. Inst., vol. xi., p. 428. Sir James Hector says, “flowering 5th December,” “capsule not seen.” His specific description of the plant is consequently imperfect, but his account of its discovery, &c., is interesting and worthy of perusal.

[Footnote] † See Trans. N.Z. Inst., vol. xviii., p. 258: P. amœna, Col., and P. phylicifolia, Lodd.

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Order XXII. Leguminosæ.

Genus 1. Carmichælia, Br.

1. C. multicaule, sp. nov.

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

Shrub about 10ft. high erect, many stems close together from one rootstock, the thicker ones being about 3in. diameter and very irregularly grooved and corrugated, bark smooth; stems below for 3ft.–4ft. from ground bare of branches; above the branches are very numerous suberect and dependent; the smaller branches long slender terete sub 1 line diameter, slightly geniculate; branchlets very numerous, alternate about 1in. apart, the ultimate ones simple straight 7in.–10in. long, very narrow 1/20;in. broad, dark-green, striate, with small scarious marginal bracts ½in.–¾in. apart. Leaves 0. Flowers not numerous, on some large branches none, alternate in small panicles containing 7–11 flowers ½in.–1in. apart; peduncle with 1 deltoid brown bract at base slightly cut; pedicels 1–2 lines long, slender, much pilose, margins densely ciliate, hairs pure-white, striking, with many small scattered brown bracteoles. Calyx rather large, free, inflated, green, glabrous, submembranous, margins toothed; teeth black very prominent. Corolla small open variegated; standard oblate-orbicular 2 lines broad, largely retuse, much recurved, dark blue-purple with white margin, veined; wings linear-oblong thin white, longer than keel, their tips broad rounded, reddish; keel subreniform 1½ lines long, whitish, tip rounded pale-reddish. Filaments very slender capillary, pellucid membranous, flexuous; anthers small, elliptic, fawn-coloured; style very long, curved, persistent; stigma rather large, capitate, thickly puberulous. Pod narrow-oblong 4 lines long including long stout beak, glabrous, dark-green young; beak very stout subulate, 1–1¼ lines long, sublanceolate contracted at apex of pod.

Hab. Open grassy flats in gullies south of Dannevirke, County of Waipawa; 1889–92: W. C.

Obs. This shrub is peculiar from its habit and manner of growth; its main stems are curious objects, being so close together and numerously and largely furrowed with their bark unbroken. I have long known the plant, and have often visited them seeking flowers or fruit, but have always been disappointed until this year, 1892, when, in November, I was gladdened on seeing many healthy young flowering buds showing themselves; fortunately I secured some specimens, though very young, and when I visited again before Christmas (almost purposely) I found but very few flowers and immature pods, and these only on one of the many branches. Of all the others I had seen the month before, there was now no trace. It is evidently allied to C. corymbosa, Col. (Trans. N.Z. Inst.,

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vol. xxi., p. 80), but differs in several characters. Sheep rest under its shade, and cattle browse on its young drooping branches, often without biting them off, owing to their toughness, leaving an unsightly chewed mass of dead hanging fibres; just as they do with chewed Phormium leaves, and the young flowering-culms of Arundo conspicua.

Order XXXIX. Compositæ.

Genus 1. Olearia, Mænch.

1. O. fasciculifolia, sp. nov.

A low bushy shrub, 4ft.–5ft. high. My single specimen, top of a branch 6in. long, contains many close subdecussate branchlets, from 5in. to 1in. in length, the longer ones being again branched. Branchlets erect and suberect, slender, straight, opposite, semi-whorled, angled; bark reddish-brown, striate, with more or less of orange-coloured dry waxy exudation, which is also scattered on leaves and more largely on involucre. Leaves few, distant, fascicled in 3 and 4, opposite, erect and patent, linear-oblong or sub-linear-spathulate, 1½–2 (rarely 3) lines long, less than 1 line wide, thickish, tip rounded, base tapering, margins entire narrowly revolute and appressed, dark-green glabrous above, greyish-white below with closely-appressed hairs; lower half of midrib prominent below; petiole short, stout. Heads single, scattered, axillary on lower half of branchlets, sometimes 2 together subfascicled, campanulate, 2 lines diameter; pedicels short, sub 1 line, stout. Involucral scales many, imbricate in 6–7 rows, orange-coloured with blackish dark-green central stripe, the lowermost small, obtuse; middle much larger, ovate, acute; innermost row very narrow acuminate, 2–2½ lines long. Florets few, produced beyond pappus, black when dry, very slender, weak, subreflexed. Pappus scanty, straight, glossy, nearly equal, scabrid, white, tips acute. Achene semi-terete, linear, 1 line long, grooved, thickest at top, pale, glabrous, shining. Disc smoothish, shining, pitted.

Hab. Open lands between Dannevirke and Weber, County of Waipawa; 1892: Mr. H. Hill. Flowering late in May.

Genus 17. Senecio, Linn.

1. S. multinerve, sp. nov.

“A low spreading shrub, about 4ft. high.” My specimen, a branch 9in. long (torn off from a larger one), shortly spreading into 3 slender erect branches, glabrous (and slightly-scattered puberulent whitish hairs), bark furrowed reddish-brown. Leaves few, distant, scattered, thin, spreading, oblong-lanceolate and linear-elliptic, 1in.–1¾in. long, 4–6 lines broad, tips very obtuse subtruncate, base tapering, glabrous above,

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slightly scabrid-puberulous below; margins thickened, coarsely and closely toothed, teeth knobbed; veins below very reticulate and dark; petioles slender, 4–8 lines long, grooved above, puberulent. Flowers bright-yellow, close, showy, in terminal corymbs beyond leaves; peduncles 1in.–1¼in. long, filiform 3-flowered, with a long narrow leafy bract at base; pedicels spreading, slender, 4–5 lines long, a long bract at the base and 2 linear bracteoles above the middle. Heads rather small, campanulate, 4 lines long. Involucral scales 5, oblong, slightly puberulent above, the 2 inner very broad 4-nerved, with, large membranous margins, their tips rounded and ciliolate, the 3 outer narrower. Florets few 7–8, 2–3 ray, 5 disc; lamina of ray broad for size of flower, 7-nerved, tips revolute. Pappus numerous, a little shorter than florets, rather harsh, glossy, white, scabrid, unequal. Achene linear, glabrous, obsoletely ribbed dark-brown. Disc alveolate, edges raised rough.

Hab. In a valley near Tolaga Bay, East Coast; rare; 1892: Mr. H. Hill.

Obs. This plant is certainly closely allied to S. perdicioides, Hook. f., also a very rare plant from that same locality, discovered by Banks and Solander on Cook's first visit to New Zealand. I have been in doubt about describing it as being distinct; but there seem to me to be certain grave characters pertaining to it, which, if in S. perdicioides, could not have been unnoticed by Hooker, as—its margined and knobbed leaves (which are also of a different form), its peculiar and handsome inner scales of the involucre, and its long bracts and bracteoles.

Order XLII. Ericeæ.

Genus 8. Dracophyllum, Labill.

1. D. imbricatum, sp. nov.

(My single specimen) a branch 17in. long, simple, straight, stout, as thick as a goosequill at base, base there for 3in.–4in. with dark-brown bark, light-reddish and ringed above where denuded under leaves—apparently a strong, healthy, vigorous young branch. Leaves numerous, close, erect and squarrosely spreading, linear, 4in.–5in. long, 4 lines wide, rather thin yet opaque, smooth, dry, concave, pale-green, glabrous, margins slightly and closely serrulate, tapering to apex, tip long, very narrow and acute, bases dilated ½in. wide, reddish, imbricate and largely amplexicaul; the upper leaves erect extending as high as panicle. Flowers terminal in a narrow contracted erect raceme-like panicle, 2in.–2½in. long, sub ½in. wide; bark glabrous, dark-brown, much grooved; few flowers, 3–4 on short branchlets, each branchlet with a long linear bract at

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base, keeled and submucronate; pedicels about 1 line long; calycine bracts half as long as corolla, ovate, concave, finely serrulate, tips produced, acute. Corolla 4 lines long, narrow campanulate, reddish-orange, lobes shorter than tube, subdeltoid-ovate, lateral margins much incurved, whitish, tips narrow revolute. Anthers linear-elliptic, 2-lobed, included; filaments free twice as long as style; style 1 line long, slightly puberulent, stoutish, cylindrical, simple; hypogenous scales sub-linear-ovate (or lingulate), broadest at base, truncate and notched at tip. Ovary very small, scarcely 1 line diameter, with 5 minute rounded protuberances at top.

Hab. Open lands near Cape Runaway, east coast, North Island; 1892: Mr. H. Hill.

Obs. Apparently this striking species is allied to D. strictum, Hook. My specimen is a large one, though sadly crushed in long carriage in a saddle-bag, especially its more tender flowering part; sufficient, however, remained to enable me to describe it. Better flowering and fruiting specimens are wanted; also to know more about the size and shape of the shrub.

Order LIII. Scrophularineæ.

Genus 7. Veronica, Linn.

1. V. darwiniana, sp. nov.

A small neat glabrous shrub, with short spreading opposite simple branchlets, their bark light-brownish-green, with a narrow longitudinal pubescent line decurrent from bases of each pair of leaves to the next pair. Leaves subdecussate, distant, regular, subconcave, thickish, glaucous-green, minutely and thickly dotted with whitish specks on both surfaces, broadly-lanceolate, 8–9 lines long, 2.½–3 lines broad, not keeled, sessile, tips acute, blunt, margins entire lighter green (or yellowish-green). Flowers subterminal in 2–4 opposite axillary racemes, having a subcorymbose appearance; racemes short sub 1 in. long, the flowers very thickly set; peduncle 6–7 lines long, pubescent, as also are pedicels and bracts; pedicels sub 1 line long; bracts ovate acute submembranous, adpressed, longer than pedicel. Calyx glabrous, lobes broadlyovate, green with white membranaceous margins, tips ciliolate. Corolla white, 3 lines diameter, lobes incurved obtuse, the 3 larger oblong, the upper solitary, the lower lobe very small; tube 1 line long, throat puberulous; anthers largely exserted; purple; style slender, patent, 4 lines long; stigma small, penicillate. Capsule dorsally compressed, 3 times as long as calyx, broadly-ovoid turgid, red-brown, veined; valves 2-fid, gaping; seeds numerous, orbicular and broadly-elliptic, disc form thickest in the middle, light-brown, glabrous, shining.

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Hab. On hills in the interior, Hawke's Bay; 1890–92: W. C.

Obs. I. A species primâ facie near to V. colensoi, Hook., but differing in several particulars—as, leaves smaller, subconcave and of another form; flowers pedicelled, bracts thin and longer than pedicels; lobes of calyx thin and ciliolate; corolla lobes very different, with puberulous throat; capsule larger, &c.

II. Named in honour of the illustrious Darwin who visited New Zealand, with Captain Fitzroy, in H.M.S. “Beagle,” in 1835, and with whom I had the honour and pleasure of spending Christmas Day in that year.

2. V. oligantha, sp. nov.

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

Plant small herbaceous slender simple glabrous, suberect and decumbent, 3in.–6in. high, sometimes with a very few small branches, main stems and pedicels closely and finely puberulent. Leaves few rather distant, pale-green, broadlyovate and broadly-elliptic almost suborbicular, 2.½–3.½ lines long, 2–2.½ lines broad, margins cut-crenate, and those of the upper and calycine leaves finely ciliolate, tips obtuse rounded; midrib below keeled prominent; 3-nerved, largely veined, veins compoundly-anastomosing; petiolate, petioles sub 1 line long. Flowers very few, distant, small, single, axillary in cauline leaves in the upper part of the stem and terminal, usually 3–4 pairs, the lowest pair opposite, the upper ones alternate, pedicelled, pedicels erect stout nearly 2 lines long. Calyx 4-cleft to base, segments oblong, obtuse, 1-nerved, shorter than corolla. Corolla pale, small, 1.½ lines long, tube very short scarcely any, segments all rounded the upper one the largest; much veined, veins forked. Stamens long curved; anthers large exserted, orbicular, claret-coloured; style very long, longer than capsule, filiform, persistent; stigma large capitate. Capsule fawn-coloured, sub-reniform-orbicular 1/10in. broad, compressed, notch shallow with a few erect glandular hairs on upper margin. Seeds very minute, 50 and upwards in each capsule, oblong, thickish, centrally attached, palefawn colour.

Hab. Among grasses and other low herbage, banks of streams, edges of woods, south of Dannevirke, County of Waipawa; 1892: W. C.

Obs. Another small herbaceous species of this genus to be added to those already lately described by me (Trans. N.Z. Inst., vol. xxiv., pp. 391–393), and, though pretty closely related to them, distinct from all; perhaps V. macrocalyx is its nearest ally. This little plant is somewhat striking at first sight ffom its very pale-green leaves, and also, on examination, from the great regularity of its few flowers 3–4 pairs, of which, how-

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ever, only a single corolla may be found on each stem at one time; no doubt owing to the extreme shortness of its tube, which causes it to fall quickly off on the enlargement of its ovary.

Class II. Monocotyledons.

Order VII. Liliaceæ.
Genus 3. Cordyline, Commerson.

1. C. hectori, sp. nov.

Trunk arboreous, simple, erect, from 6ft. to 30ft. high. Leaves numerous erect and spreading all round, linear- lanceolate, 4ft. 10in. long, 6.½in. wide at middle, gradually contracted to 4in. wide at 7in. above base, and again expanding to 5.½in. at base, acute not acuminate, rather thin for size (chartaceous), somewhat softish (not harsh, as in Phormium and in C. australis), but very thick at base, closely striated, margins entire, red thin and slightly recurved, glabrous, greenish-purple above with a reddish hue, and glaucous below with red veins; veins very numerous, above 100 on either side of midrib, parallel, slightly and regularly diagonal, extending nearly the whole length of lamina, and of three kinds—viz., (1) stout red prominent shining, distant about ¼in. from each other; (2) smaller and finer, intermediate and reddish; (3) obsolete again intermediate and glaucous; the midrib red glabrous and glossy, very stout and large at base and for some distance above, but decreasing regularly towards apex and there vanishing, striate-veined on the under-surface for two-thirds length from base. Panicle pendulous, obovate, thick compressed, 16in. long and 17in. girth over all; peduncle (or main stem) 4in. long,* thick 3.½in. girth; subpanicles (simple racemes) numerous, straight, obfastigiate, imbricate, each 7in. long, linear-acuminate, 2.¾in. girth, a single bract at base 1.¾in. long, 4 lines wide at base, many-nerved, subulate, acuminate, acute. Flowers very numerous and close together; pedicels stoutish, thickened at top, 2 lines long, with 2 bracteoles on each, the outer one the longer, 3 lines long, sub-linear-ovate, 1-nerved, tip subacute, the inner one broader, irregularly shaped, semi-amplexicaul, apex sometimes retuse, and 2–3-fid, acute, acuminate, very membranous. Perianth small, sub ½in. diameter; segments narrow-oblong, split to base, subequal, much recurved, 3-nerved, nerves prominent. Stamens broad and flat at bases, adhering to lobes one-third of length from base, shorter than style, slightly incurved over ovary; anthers linear-elliptic. Style sub 2 lines long, stout, grooved. Berry globose nearly 2 lines diameter, glabrous,

[Footnote] * But I have not got the whole of it, only that portion which forms part of the panicle, and where the pedicels with flowers begin.

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blue; about 16 seeds in each; seeds black, shining, usually 3-sided, flat on two sides and rounded on the third, but when fewer in number gibbous.

Hob. “On the spurs and in the gullies of the Ruahine, Kaweka, and Kaimanawa Mountain-ranges, County of Hawke's Bay; alt. 2,000ft.–4,000ft. Sometimes growing in the woods, and sometimes in the open lands, but more generally along the edges of woods, and among scattered shrubs.”—Mr. Thomas Hallett, in lit., August, 1892.

Obs. I. Mr. Hallett also says in his interesting letter, “These trees vary in height from 6ft. to 30ft. but are generally about 12ft. high in open lands, and 20ft. in woods. The flowering - stem hangs down beside the trunk of the tree. The leaves sent were cut from a tree growing at 2,100ft. alt. above sea-level, and at about 7ft. above ground; there were 60 of them besides the small unfolded central ones; the diameter of the trunk was 6in. Each leaf in falling off leaves a ring on the stem, which becomes very indistinct after a few years; and, as several leaves grow every year, there are many rings formed, so that the age of the plant cannot be determined by them.”

II. I have long known this plant–from my first seeing it in its native habitat in the 30s, and often afterwards in the 40s, when travelling in the mountainous interior of this North Island, and also in following years occasionally cultivated in gardens* —but had never seen its flowers; and from the description of Forster's plant, C. indivisa, obtained by him in the South Island (as given by Hooker), I always had a doubt of it being the same species as this one, which doubt was also further increased through my certain knowledge that Forster had never been in this North Island. And when I read “the valuable communication regarding the Cordylines” made by Sir James Hector to Sir Joseph Hooker, † I felt pretty well confirmed in my opinion. Sir James Hector wrote,—

“5. C. indivisa. This is the broad-leaved deep-green ti, with red veins, a single head, and long elegant flowers, that Forster found in Dusky Bay. The leaf has a slight resemblace to the true toii of Colenso, which has led to the confusion, no doubt.

[Footnote] * I had for several years fine plants of it growing well in my garden at Waitangi (Hawke's Bay), with other mountain plants, as Ranunculus insignis, Aciphylla colensoi, Calceolaria repens, Cordyline banksii, Anthericum hookeri, &c. All these flourished and flowered there until a very severe and long continued flood, which overflowed my garden and deposited a large amount of silt, which destroyed them all.

[Footnote] † “Handbook of the New Zealand Flora,” p. 743.

[Footnote] ‡ Ti is the Maori name for the Cordylines; it may be called their generic one.

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“6. C. sp.? Toii. A large tree, with many heads, and huge broad massive leaves, yellowish, with yellow and red veins, and ponderous inflorescence with long bracts and black shiny seeds. This is the ti that the Natives use for mats, &c. The portion of the description of the Handbook which refers to C. indivisa, and which you got from Colenso, applies to this plant.”

To this Sir J. Hooker adds, “I have no Dusky Bay specimens of Forster's plant, but Colenso's agrees well with Forster's figure in the British Museum” (loc. cit.). And in my fully describing this northern species of Cordyline I have also, with very great pleasure, named it in honour of our wellknown scientific naturalist, Sir James Hector, K.C.M.G., M.D., F.R.S., &c., who had not only seen both species growing in their native habitats in his travels in the North and South Islands of New Zealand, but had at an early date (prior to 1864) called Sir Joseph Hooker's particular attention to their specific differences.

III. From time to time of late years I have made several endeavours to obtain both flowering and fruiting specimens of our northern subalpine Cordyline, but have always failed until this present year (1892), when, through Mr. Hallett's kindness and care, I obtained what I had so long sought; I having long known him, and he being a resident settler far away in the hilly interior, and pretty near the home of these plants, and well acquainted with them. To him I feel much indebted for the several packages of specimens in various states he so readily obtained and sent me, though at no small trouble and labour to himself, as well as for his interesting notes and letters concerning the plant. And, not being satisfied with the specific description of C. indivisa as given by Hooker, both in his “Flora Novæ-Zelandiæ” and in the Handbook, and not possessing the fifth volume of Kunth's “Enumeration” (though I have vols. 1–4), and finding, on inquiry, the said fifth volume was not here in the colony, I got a kind naturalist friend to write to Berlin to get a verbatim copy made from Kunth's work, and this I received a few months back, which with me settled the question concerning the specific differences of the two plants.

IV. In conclusion, I may observe that several striking primâ facie characters in this species here described do not accord with those of C. indivisa (vera), Kunth: e.g., Sir James Hector mentions its “long elegant flowers” (loc. cit.), and Sir Joseph Hooker also calls them “the large flowers,” with “its excessively thick and coriaceous leaves” (Handbook, p. 282), which leaves, however, are really smaller, as described by Kunth, who says of them, “2–4 pedes longa, medio 4–5 polli-caris, supra basin 1.½–2 poll. lata, rigide, coriacea”; and, further,

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the panicle as being much larger—“3–4 pedalis”—with other differences, as “ovula in loculo 5–6,” and the plant to be “10–20 pedalis.” (“Enum.,” v., 30.)

Genus 6. Arthropodium, Brown.

1. A. ramulosum, sp. nov.

Plant small, slender, glabrous. Leaves 10, prostrate, spreading around stem subrosulate, linear-lanceolate, 9in.–10in. long, 3 lines wide, 3 innermost widest, concave, very acuminate tip acute, base half-clasping, membranaceous, flaccid, somewhat curved or subfalcate, dark-green, much parallel-nerved and striate on under-surface and so the cauline leaves. Stem single, erect, 18in. high, purple, slightly geniclate at nodes, 12-branched, base 1.½ lines diameter, apex flowering; branches green, striate, alternate, distant, the lower ones 7in. long, decreasing gradually in size upwards, the uppermost 3.½in. long at 4in. from tip of stem, spreading horizontally; the lower branches. 2in. apart on stem, the upper ones sub 1in.; no branch at lowest node 1.½in. from base, but a simple very long cauline leaf or bract 7in. long; at the lowest node of the basal branch a branchlet 1.½in. long 2–3-flowered, and at 2 nodes next above on same branch 2 flowers from each (this peculiarity also occurs at the lowest node of the apical portion); at the base of each branch are 2 leaf-like cauline sessile linear-acuminate bracts, the longer one 5in. long 3 lines wide, with a minute lilac-coloured membranaceous bracteole in the axil between branch and stem (also in the axils of all the branches), 2-nerved, tip acute and bifid. Flowers scattered, generally 12 on the longer branches each ¾in.—½in. apart; pedicels ½in. long, slender, jointed above middle, all bracteolate with long green bracteoles. Perianth small white, segments 2 lines long, narrow-oblong nearly alike, reflexed, each having 3 faint longitudinal medial lines (or nerves) parallel and close, the 3 outer segments stouter margins entire, tips subacute and thickened, the 3 inner very membranous margins slightly denticulate-erose, tips truncate; filaments white shorter than perianth 1.½lines long erect spreading, their upper two-thirds densely hairy bushy throughout, extending close up to anther; hairs white stout, glistening, tips obtuse; anthers small ½4in. long, pale, linear; style erect a little longer than anthers; stigma simple, capitate, flat, spreading; ovarium green glabrous scarcely 1 line long rounded-oblong.

Hab. In a rocky spot near Mangatoro, south of Dannevirke, County of Waipawa; 1892: W. C.

Obs. I. This is a striking and graceful species, having

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affinity with A. candidum, Raoul, and A. reflexum, Col.,* but widely different from both in habit and in general appearance and in several important characters. Its leaves (both radical and cauline) are larger and differently shaped and coloured (not like common grass leaves); stem much taller and 12-branched; branches very long and patent (and sometimes again branched); flowers smaller with different perianth-segments and anthers. But while the differences are many and great they are difficult to accurately describe in words, though soon apparent on examination and comparison with the above-named two species. This plant is also allied to a New Caledonian one—A. neocaledonicum, Baker. It also possesses in a a striking degree that peculiar quality I had noticed in A. reflexum (l.c.), of only one flower (on a branch) opening at one time, and this in early morning, and so remaining until evening, when the perianth falls down, resuming its former position, and closely enwraps the ovarium, as in the other plant.

II. I have only seen this one specimen here described, and the peculiar (almost unique) manner of my getting it deserves a brief notice. In June, 1892 (during a long wet winter season), I received a dripping muddy parcel of small ferns and other low herbaceous plants, roots and all, in tufts, as torn up from their low and wet habitat (the friend who sent them was there on a geological visit). It took me some considerable time to wash and clean them, and while so engaged I found a very small unequally semi-fascicled or trilobed root (less than a shilling in circumference), without any traces of leaves, stem, &c., and apparently half-dead: this, however, I kept and planted, and this neat plant has been evolved from it. So I am rewarded.

Art. XLIV.—A List of Fungi recently detected and collected in the Bush District, County of Hawke's Bay; being a Further Contribution to the Indigenous Flora of New Zealand.

[Read before the Hawke's Bay Philosophical Institute, 28th November, 1892.]

In January last I despatched to the Director of the Royal Botanic Gardens, Kew, London, another lot of Fungi that I had gathered at various times during the preceding year in the forest country around Dannevirke. This parcel contained

[Footnote] * Trans. N.Z. Inst., vol. xviii., p. 275.

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about two hundred separate packets. The Director, Mr. Thiselton-Dyer, soon put them into the hands of Dr. Cooke, the eminent fungologist, for examination and determination, as he had also done on former occasions.* I have recently received from Kew the list of the same, as kindly named by Dr. Cooke; from which it appears that most of them were duplicates of those I had formerly transmitted, several, however, being better specimens, and also in different states of age and growth. These that are new to our New Zealand flora are here given; few of them I take to be really species novœ.

1.† Agaricus, Linn.

  • (Pleurotus) bursæformis, B.

  • (Pleurotus) diversipes, B.

  • (Pleurotus) sordulentus, Fr.

  • (Collybia) laceratus, Lasch.

  • (Pluteus) cervinus, Fr.

  • (Pholiota) unicolor, Fr.

  • (Pholiota) pumilus, Fr.

  • (Flammula) vinosus, Fr.

  • (Flammula) crociphyllus, C. and M.

  • (Flammula) purpureo-nitens, C. and M.

  • (Lepiota) imperfect.

  • (Leptoma) æthiops, Fr.

  • (Clitocybe) laccatus, Fr.

  • (Psathyrella) disseminatus, Fr.

  • (Leptonia) placidus, Fr.

  • (Stropharia) semiglobatus, Fr.

4. Marasmius, Fries.

M.

hematocephalus, M.

10. Polyporus, Fries.

P.

isidioides, B.

16. Stereum, Fries.

  • amænum, Kal.

  • obliquum, B.

27. Geaster, Micheli.

G.

subiculosum, C. and M.

30. Lycoperdon, Tournefort.

  • australe, B.

  • perlatum, Fr.

  • constellatum.

[Footnote] * See lists, Trans., N.Z. Inst., vol. xvii., p. 265; vol. xix., p. 301; and vol. xxii., p. 391.

[Footnote] † The numbers attached to the genera are those of the same in the “Handbook of the New Zealand Flora.”

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50. Æcidium, Persoon.

  • Æ. gallii, P.

60. Peziza, Dill.

P.

campylospora, B.

68. Hypocrea, Fries.

H.

rufa, Fr.

73. Nectria, Fries.

N.

ditissima, Tul.

Tremella, Fries.

T.

fuciformis, B.

Trichia, Hall.

T.

affinis, R.

Polystictus.

  • decipiens, Schw.

  • hirsutus, Fr.

  • drummondii, B.

Fomes.

  • zealandicus, Cke.

  • annosus, Fr.

Poria.

P.

nitida, Fr.

Actinonema.

A.

rosse, Fr.

Patellea.

P.

adamsoni, B.

Helvella.

H.

monachella, Fr.

Synchytrium

S.

melicopidis, C. and M.

Xerotus.

X.

glaucophyllum, C. and M.

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Art. XLV.—Memorandum of a few New Species of Hepaticæ lately detected in the Seventy-mile Bush District; as kindly determined by Dr. F. Stephani, of Berlin.

[Read before the Hawke's Bay Philosophical Institute, 28th November, 1892.]

In forwarding to Kew the Fungi mentioned in the preceding paper, I also sent a lot of Hepaticœ that I had collected at various times and seasons with them. These were put by the Director at Kew into Dr. Stephani's hands for examination and determination, as on a former occasion;* and I have recently received from Kew a list of them (but without description), and also a long enumeration of many others sent with them that have been already described in the “Handbook of the New Zealand Flora,” in several volumes of the Transactions of the New Zealand Institute, and also in some modern European works.

The species really new to science are only four, while five others that were known have now been found in New Zealand; there were also a few others that were barren or too imperfect to be named, and many that (according to Dr. Stephani) were very fine and interesting.

Moreover, Dr. Stephani's remarks (of several species)—“There have been two forms sent of very different appearance, the normal one growing in places exposed to sunlight, stout and tough very dark, in a dry state almost black and horny, lobules large; while a common variety growing in dark forests is flaccid quite green, lobules small,” &c.—are worthy of being copied here.

I.Species novœ:–

  • Symphyogyna subpetiolata.

  • Aneura papulosa.

  • Anthoceros arachnoideus.

  • Lophocolea erectifolia.

II.Species already known, but hitherto not from New Zealand:–

  • Metzgeria crassicostata, St.

  • Lepidozia quadrifida, Ldbg.

  • Bazzania mittenii, St.

  • Balantiopsis diplophylla, Mitt.

  • Porella stangeri, L. et G.

[Footnote] * See Trans. N.Z. Inst., vol. xxiv., p. 398.

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III. Species also in the same lot, already described by me (in the Transactions of the New Zealand Institute), and now confirmed by Dr. Stephani as valid species novœ:–

  • Symphyogyna undulata.

  • Aneura bipinnatifida.

A.alba.

  • Fossombronia perpusilla.

  • Bazzania elegans.

B.nitens.

Also, my Symphyogyna connivens has been altered to Pallavicinia connivens, St., and my Zoopsis tenuicaulis to Zoopsis leitgebii, Carr et Pears.—very likely from specimens I had early sent them.