
Genus Cœlostoma, Maskell.
Cœlostoma pilosum, sp. nov. Plate VII., figs. 1–10.
Adult female dark-red in colour. At first naked; then with a thin covering of white meal, which gradually becomes thicker and more solid, until it assumes the appearance of a hard, granular shell, looking like a coating of lime: at gestation this increases to a snow-white mass of closely-felted cotton covering the insect and the eggs. Length of insect variable, some specimens attaining a length of ½ in., shrivelling at gestation. Form elliptical, convex, distinctly segmented. Antennæ of eleven sub-equal joints, each joint except the last very slightly dilated towards the tip, the last joint ovate; all the joints bear hairs, and on the last are two stronger than the rest. Feet strong and thick; on the trochanter a long seta; all the joints bear several hairs, but there seems to be no distinct comb of spines on the inner edge of the tibia and tarsus; the claw has a minute tooth. Upper digitules absent; lower pair fine hairs. Epidermis thickly covered with longish hairs interspersed with small, simple, circular spinneret-orifices. Anogenital ring simple: at the extremity of the abdomen are two very small tubercles, with a shortish seta on each. Rostrum and mentum entirely absent, being replaced by a small orifice between the first pair of feet.
Female of second stage dark-red in colour, covered partially or wholly with a hard, white coating, like lime, which frequently at last exhibits marginal tuberosities forming a kind of thick fringe. Length variable, reaching sometimes ⅛in. when extracted from the shell. Form elliptical, slightly convex, segmented. Antennæ atrophied: they may have six or eight joints, but these are so confused that it is difficult to determine the number; at the tip are several spiny hairs. Feet also atrophied, the joints apparently reduced to two, with a very small hook-like claw at the end. Rostrum and mentum very large: mentum conical, triarticulate. Epidermis very thickly clothed with longish rather thick hairs, interspersed with small, simple, circular spinneret-orifices. Anal extremity not exhibiting a brown patch; the anal ring simple, with the tubular internal organ usual in the genus, and frequently a long, slender, white, waxy filament.
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Larva red, active, naked or with thin white cotton; elliptical, flattish, segmented; length about 1/40in. Antennæ of six

joints—the third, fourth, and fifth the shortest, the sixth very large, ovate, with a small projection at the tip. Feet rather thick; digitules four, all fine hairs. Mentum large, conical, triarticulate; setæ very long. Abdominal extremity bearing two small tubercles, each with a long seta, and two or three spines; between the tubercles protrude two rather thick pencils of white cotton. Epidermis not thickly clothed with hairs, but on each segment is a single transverse row of small spiny hairs with some small simple circular spinnerets.
Male unknown.
Hab. On various trees in forests, Reefton district, New Zealand. The second stage mostly on Podocarpus totara or various species of Fagus.
This insect is easily distinguished from C. zealandicum by the snow-white shelly covering both in the adult and the second stage, and by the thick coating of hairs on the epidermis. The larva is much smaller than that of C. zealandicum, and, curiously, it differs also in being much less hairy, quite the contrary of the second stage. I do not think that this can be the female form of C. wairoense, because the peculiar brush of digitules which distinguishes the male of that species has no counterpart in C. pilosum; and as far as my experience goes such a character would in all likelihood be shared by both sexes. The female of C. wairoense and the male of C. pilosum may both be discovered some day.
Cœlostoma assimile, Maskell. N.Z. Trans., vol. xxii., p. 153. Plate VII., figs. 11–17.
In my paper of last year I gave a brief description of the second female stage of this insect; I am able now to complete it, and to add also the adult female and the larva.
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Adult female reddish-brown, occupying a deep pit in the twig it lives on (mostly in the axils), the mouth of the pit being covered, with the mass of thick yellow wax, of irregularly globular shape, already formed by the second-stage female. The cavity burrowed out is frequently quite deep in the bark, and even seems sometimes to extend into the wood. The dimensions vary: some of the waxy coverings are only about 1/15in. across; others observed reach ⅛in. The wax is very hard. The adult female at first, after discarding the pupal skin, occupies the whole space, and is globular, with a diameter of about 1/16in., obscurely segmented; but at gestation it shrivels up into an extremely small shapeless mass, filling the cavity with red oval eggs, and becoming at last so shrivelled that it is extremely difficult to find her. Antennæ short, thick, atrophied; the joints apparently only five, but the fifth may be made up of several, so that the normal antenna would have

eleven joints, as usual in the genus: the third and fourth joints are very short; the fifth long, sub-conical, with three or four, spiny hairs at the tip: as the third and fourth joints are the thickest, the antenna is somewhat elliptical. Feet absent. Rostrum and mentum entirely wanting. Epidermis covered with very slender hairs, which are sparse on the cephalic and thoracic regions but very numerous on the abdomén, and also with many small, simple, circular spinneret-orifices. Spiracles sixteen, four of which, on the cephalic region, are very large. Anogenital ring simple, with a tubular organ leading to it, as usual in the genus; at each side of the ring is a sub-circular scar or orifice of the same dimensions.
Female of the second stage as described in my last paper (vol. xxii., p. 153). I omitted, however, then to state that from the anogenital ring and tubular organ there springs a long, white, slender filament. This filament is sometimes more than an inch long: it protrudes through the waxy covering, and at the extremity there is often seen a minute bubble of honey dew. The filament is excessively brittle, and pieces broken off are frequently observed on the adjacent twig. At the metamorphosis the exuviæ of this second stage remain in the cavity, and become flattened and disc-like: on breaking open the waxy test in late autumn, when the eggs have been laid, this pupal skin is usually the first object visible, covering the eggs, and, as the adult female (as stated above) has shrivelled up, the skin may be at first mistaken for the adult, but the presence of the very large rostrum and mentum at once shows the real state of the case. The filament already mentioned frequently remains protruding, and is found to be attached to this pupal skin.
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Larva red, elongated, sub-elliptical, tapering somewhat posteriorly, active, sparsely covered with thin white cotton; length about 1/35in. Antennæ of six joints—the first five cylindrical, sub-equal; the sixth very large, ovate. Feet with rather thick femora and tibiæ; tibia shorter than tarsus; claw slender, with a tooth on the inner margin; no tarsal digitules, the lower pair long, fine, with a slightly-dilated tip. Mentum large, conical, triarticulate, with a few hairs at the tip. Epidermis bearing many simple circular spinneret-orifices, which are most numerous in a circular patch at the abdominal extremity, with the usual tubular organ bearing three rings of glands; at the extremity are two very small anal tubercles, each bearing a long seta, and from the tubular organ there protrudes between the tubercles a thickish pencil of white cotton.
Male unknown.
Hab. On Fagus menziesii, Phyllocladus trichomanoides, and Fagus fusca, Reefton district. It appears to be not

uncommon in that region. The waxy tests are very small and inconspicuous.
The finding of the adult female enclosed in the waxy mass formed by the female of the second stage was a surprise to me, being a distinct departure from the normal condition of things, especially in the group Monophlebidæ. It affords a good instance of the necessity, as I take it, of thorough examination of all stages before any absolute certainty can be arrived at, even as to the generic position of an insect. Whatever may be the rule amongst other orders and families of insects, Coccids present this difficulty to students: that one must be prepared at any time to find very distinct departures from generic, or even group, types, and to consider any character whatsoever as elastic and variable. Thus, for example, in the Dactylopidæ, the insect described in my last paper under the name D. obtectus departs entirely from the generic type in employing a portion of the plant it lives on as a shelter or “scale” for the adult female. So, again, in the Monophlebidæ, no genus or species has been reported hitherto in which the adult female is not, at least before gestation, free and active, or only covered with loose cotton. Cœlostoma assimile departs altogether from the types of the group and the genus in remaining under the thick waxy test in its adult state; and the variation is emphasized, so to speak, by the absence of the feet. The characters, however, of the larva and of the second stage being so clearly those of the genus Cœlostoma, and the rostrum and mentum of the adult being entirely absent, I have no hesitation in retaining the insect in that genus despite the form of the antenna; and, indeed, this may be looked on as merely atrophied.
The deep cavity made by this species in the wood of its tree, and its usual position in the axils of the twigs, make it resemble Xylococcus filiferus, Löw (Verh. der zool.-bot. Gesellschaft, Wien, 1882), which insect also has a small covering of wax, and a very long slender filament protruding from the abdominal extremity. But the presence in Xylococcus of a very distinct rostrum (which, indeed, seems to be the only member preserved by the adult female) clearly distinguishes that genus from Cœlostoma; and, indeed, the forms of the larva and of the second stage are also quite different.
The late Dr. Löw, whose death a few months ago deprived entomology of one of its brightest ornaments, devoted some remarks in his description of Xylococcus filiferus to the question of the manner in which that Coccid managed to produce a deep cavity in the wood of its food-plant, Tilia europæa. He was, however, unable to give any other explanation than that it proceeded “by a most peculiar kind of suction, and besides by a certain influence which these insects exercise on

the plant-growth.” In fact, when it is considered how entirely devoid Coccids of all genera are of any organs for piercing or cutting, except the rostral suckers, it is difficult to understand how they manage to burrow into plants. Here in New Zealand we have such species as Ctenochiton viridis, which does not indeed form a deep cavity, but produces a decided and conspicuous depression beneath its body in the leaf it lives on. Rhizococcus fossor forms a peculiarly deep pit in its leaf, pressing out the opposite surface in a distinct sweelling, and at last almost disappears sometimes in the pit. Cœlostoma assimile burrows a deep hole through the bark of the tree, and even into the wood, fashioning for itself a complete little cavern. How is all this done? In the case of Ctenochiton and Rhizococcus, living as they do on soft leaves, one might imagine that they use their feet and claws to press out the plant-cells and make the cavities; but Cœlostoma assimile loses its feet almost in its infancy, and the explanation would therefore not suffice in this case. I do not think, moreover, that any mechanical action would altogether account for the phenomenon; for in specimens of leaves and (as far as I could) of wood examined I do not see any traces of such pressure on the cells as would render them misshapen. Whatever may be the real action of the Coccid, it seems to me that it must be at the same time mechanical and chemical. There must be some chemical reason why certain species form on plants large galls, which are exactly the opposite of cavities; and in the same way some chemical action must, I think, be exerted to produce the cavities and depressions. But I can offer no plausible explanation myself; and I do not forget that, as far as is known at present, Coccids do not exude any acrid or acid fluid likely to exert active influence on plant-cells.
It may be observed that purely “passive” pressure would not sufficiently account for the phenomenon—that is, I do not think that the cavities can be produced merely by the insect lying motionless on the bark or leaf, and permitting the plant-cells to grow round and over it. Such a proceeding would necessarily, I take it, induce some kind of distortion; but I see no signs of this in the cases referred to. Moreover, in the case of C. assimile and R. fossor, passive obstruction (as it might be called) is not at all sufficient to produce in so short a time the deep pits observed. Further, such insects as Lecanium hesperidum, Mytilaspis pomorum, and scores of others, are just as closely attached to plants as any others, and yet produce no cavities in either leaves or bark, or even in the very soft substance of fruit.

