141 [In 1879 Mr. George Francis, of Adelaide, forwarded from the latter place a number of moths (a species of Anapæa) together with their larvæ (in alcohol) and cocoons (Proc. Ent. Soc. 1879, p. xvi), and in an accompanying note he stated that the male larva when living is of “a bright emerald green, with red and pink markings on the back, and yellow, black, and white streaks on the sides.” The male larva is described as being smaller than the female, and as possessing all the brilliant colours, the latter “having no red markings, but only white, yellow, and green, with a little black.” I was at first disposed to think that we might be dealing here with two distinct species having differently marked larvæ; but Mr. Francis this present year (1880) forwarded a large number of the living cocoons of this species, which I separated according to size, and, on the emergence of the moths (August), I found that all those from the small cocoons were males, and those from the larger cocoons females. There can be no doubt, therefore, that we have but one species in this case, the larva of which presents the remarkable phenomenon of sexual difference of coloration. As an analogous fact I may here mention the well-known case of Orgyia Antiqua, the larva of which differs in the colour of the tufts of hair according to sex. R.M.]
142 [I have already given reasons for suspecting that the colour of green caterpillars may be due to the presence of chlorophyll (or some derivative thereof) in their tissues (see Proc. Zoo. Soc. 1873, p. 159). This substance appears to be one of great chemical stability, and, according to Chautard, who has detected it in an unaltered state in the tissues of certain leaf-feeding insects by means of its absorption spectrum (“Comp. Rend.” Jan. 13th, 1873), it resists the animal digestive processes (Ann. Ch. Phys. [5], iii., 1–56). If this view should be established by future observations, we must regard the green colour of caterpillars as having been produced, when protective, from phytophagic variability by the action of natural selection; and the absence of colour in internal feeders, above referred to, is only secondarily due to the exclusion of light, and depends primarily on the absence of chlorophyll in their food. In connection with this I may adduce the fact, that some few species of Nepticula (N. Oxyacanthella, N. Viscerella, &c.) are green, although they live in leaf-galleries where this colour can hardly be of use as a protection; but their food (hawthorn and elm) contains chlorophyll. See also note 130, p. 293. Further investigations in this direction are much needed. R.M.]
143 [The same applies to Pseudoterpna Cytisaria, also feeding on broom at the same time of the year. The most striking cases of adaptive resemblance brought about by longitudinal stripes are to be found among fir and pine feeders, species belonging to the most diverse families (Hyloicus Pinastri, Trachea Piniperda, Fidonia Piniaria, &c., &c.) all being most admirably concealed among the needle-shaped leaves. R.M.]
144 The geographical distribution of the dark form indicates that in the case of this species also, the form referred to is replacing the yellow (green) variety. Whilst in the middle of Europe (Germany, France, Hungary) the dark form is extremely rare, in the south of Spain this variety, as I learn from Dr. Noll, is almost as common as the yellow one. I hear also from Dr. Staudinger that in South Africa (Port Natal) the dark form is somewhat the commoner, although the golden-yellow and, more rarely, the green varieties, occur there. I have seen a caterpillar and several moths from Port Natal, and these all agree exactly with ours. The displacement of the green (yellow) form by the dark soil-adapted variety, appears therefore to proceed more rapidly in a warm than in a temperate climate. [Eng. ed. Dr. Noll writes to me from Frankfort that the caterpillar of Acherontia Atropos in the south of Spain does not, as with us, conceal itself by day in the earth, but on the stems underneath the leaves. “At Cadiz, on the hot, sandy shore, Solanum violaceum grows to a height of three feet, and on a single plant I often found more than a dozen Atropos larvæ resting with the head retracted. It can easily be understood why the lateral stripes are blue when one has seen the south European Solaneæ, on which this larva is at home. Solanum violaceum is scarcely green: violet tints alternate with brown, green, and yellow over the whole plant, and between these appear the yellow-anthered flowers, and golden-yellow berries of the size of a greengage. Thus it happens that the numerous thorns, an inch long, between which the caterpillar rests on the stem, pass from violet into shades of blue, red, green, and yellow.”]
145 [For Mr. J. P. Mansel Weale’s remarks on the habits of certain ocellated S. African Sphinx-larvæ see note 129, p. 290. R.M.]
146 [Some experiments with the caterpillar of C. Elpenor, confirming these results, have been made by Lady Verney. See “Good Words,” Dec. 1877, p. 838. R.M.]
147 [The eye-spots on Ch. Nerii have thus been supposed by some observers to be imitations of the flowers of the periwinkle, one of its food-plants. See, for instance, Sir John Lubbock’s “Scientific Lectures,” p. 51. R.M.]
148 “On Insects and Insectivorous Birds,” Trans. Ent. Soc. 1869, p. 21.
149 Ibid., p. 27.
150 [Messrs. Weir and Butler inform me that they have not experimented with Sphinx-larvæ. R.M.]
151 [It appears that the nauseous character of these last butterflies is to a certain extent retained after death, as I found that in an old collection which had been destroyed by mites, the least mutilated specimens were species of Danais and Euplæa, genera which are known to be distasteful when living, and to serve as models for mimicry. See Proc. Ent. Soc. 1877, p. xii. R.M.]
152 [This bears out the view expressed in a previous note 129, p. 290, that the grotesque attitude and caudal tentacles are more for protection against ichneumons than against larger foes. R.M.]
153 These experiments, as already mentioned above, were not made with the common German lizard (Lacerta Stirpium), but with the large South European Lacerta Viridis.
154 Thus, Boisduval states of this caterpillar, which in Provence lives on Euphorbia esula and allied species:—“Its resemblance to a serpent, and its brilliant colour, permit of its being easily discovered.” This was written in 1843, long before natural selection was thought of.
155 Or some other extinct analogously-marked species.
156 [See Darwin’s remarks on the struggle for life being most severe between individuals and varieties of the same species “Origin of Species,” 6th ed. p. 59. R.M.]
157 [Compare this with Darwin’s remarks on “analogous variations,” “Origin of Species,” 6th ed., p. 125. R.M.]
158 “Zoologische Studien auf Capri. II. Lacerta muralis cærula, ein Beitrag zur Darwin’schen Lehre.” Leipzig, 1874. [The subject of colour-variation in lizards has been much discussed in “Nature” since the publication of the above mentioned essay; see vol. xix., pp. 4, 53, 97, and 122, and vol. xx., pp. 290 and 480. R M.]
159 “Über die Berechtigung der Darwin’schen Theorie.” Leipzig, 1868. See also the previous essay “On the Seasonal Dimorphism of Butterflies,” pp. 112–116.
160 [Mr. A. G. Butler has recently advanced the view that this family is not allied to the Sphingidæ, but is related on the one side to the Pyrales, and on the other to the Gelechiidæ. See his paper “On the Natural Affinities of the Lepidopterous Family Ægeriidæ,” Trans. Ent. Soc. 1878, p. 121. R.M.]
161 I am indebted to my esteemed colleague, Prof. Gestäcker, for the knowledge of this specimen.
164 [The question here also suggests itself as to why the dorsal line should not have been the primary longitudinal stripe, seeing that such a marking is almost naturally produced in many caterpillars by the food in the alimentary canal; or, in other words, why has not natural selection taken advantage of such an obvious means of producing a stripe in cases where it would have been advantageous? In answer to this I may state, that in large numbers of species the dorsal line has thus become utilized; but in the case of large caterpillars resting among foliage, it can be easily seen that light lateral (i.e. subdorsal) stripes, are more effective in breaking the homogeneity of the body than a dorsal line only slightly darker than the general ground-colour. Lateral lines are in fact visible from two directions of space. If a caterpillar thus marked be placed on a twig, these lines are visible when we look at the creature’s back or at either side. That the subdorsal are therefore the primary lines, as shown by Dr. Weismann’s observations of the ontogeny of many of the Sphingidæ, is quite in harmony with the view of their having been produced by natural selection. R.M.]
165 “Die Darwin’sche Theorie. Elf Vorlesungen über die Entstehung der Thiere und Pflanzen durch Naturzüchtung.” 2nd ed., Leipzig, 1875, p. 195.
166 [In the following species, already mentioned in previous notes, the oblique stripes are bounded at their upper extremities by a conspicuous subdorsal line:—Acosmeryx Anceus, Cram.; Sphinx Cingulata, Fabr.; Pachylia Ficus, Linn.; P. Syces, Hübn. In Pseudosphinx Cyrtolophia, Butl., the oblique white stripes, beautifully shaded with pink, run into the white pink-bordered dorsal line, so that when seen from above the markings present the appearance of the midrib and lateral veins of a leaf, and are probably specially adapted for this purpose. R.M.]
167 [The dorsal line as well as the oblique stripes is present in the caterpillar of Smerinthus Tartarinovii, Ménét.; and in Ambulyx Gannascus, Stoll., the oblique stripes are bounded above by a subdorsal line, as in the species named in the preceding note. R.M.]
168 Cat. Lep. East India Co., Pl. XI.
169 [Compare this with Darwin’s “Origin of Species” (1st. ed. p. 440), where it is stated that when an animal, during any part of its embryonic career, is active, and has to provide for itself, “the period of activity may come on earlier or later in life; but whenever it comes on, the adaptation of the larva to its conditions of life is just as perfect and beautiful as in the adult animal. From such special adaptations the similarity of the larvæ or active embryos of allied animals is sometimes much obscured.” R.M.]
170 [For Fritz Müller’s application of this principle to the case of certain groups of Brazilian butterflies see Appendix II. to this Part. R.M.]
171 [The slight variability in the colour of this pupa, opens up the interesting question of the photographic sensitiveness of this and other species, which is stated to cause them to assimilate in colour to the surface on which the larva undergoes its final ecdysis. Some experiments upon this subject have been recorded by Mr. T. W. Wood, Proc. Ent. Soc. 1867, p. xcix, but the field is still almost unexplored. R.M.]
172 “Über den Einfluss der Isolirung auf die Artbildung.” Leipzig, 1872, p. 20.
173 In some instances Deilephila Lineata has also been seen by day hovering over flowers.
174 It is true that I only reared one brood, but from this fifty specimens were obtained. It would be interesting to know whether this variety of the caterpillar is distributed over the whole of Southern Europe.
175 In this sense Lubbock says:—“It is evident that creatures which, like the majority of insects, live during the successive periods of their existence in very different circumstances, may undergo considerable changes in their larval organization in consequence of forces acting on them while in that condition; not, indeed, without affecting, but certainly without affecting to any corresponding extent, their ultimate form.”—“Origin and Metamorphoses of Insects,” London, 1874, p. 39.
176 “Grundzüge der Zoologie,” 1875.
177 [Lepidopterists are of course aware that even these distinctions are not absolute, as no single character can be named which does not also appear in certain moths. The definition in this case, as in that of most other groups of animals and plants, is only a general one. See, for instance, Westwood’s “Introduction to the Classification of Insects,” vol. ii. pp. 330–332. Also some remarks by C. V. Riley in his “Eighth Annual Report” on the insects of Missouri, 1876, p. 170. With reference to the antennæ as a distinguishing character, see Mr. A. G. Butler’s article in “Science for All,” 1880, part xxvii. p. 65. R.M.]
178 The genus of Morphinæ, Discophora, possesses hairs very similar to those of the genus Cnethocampa belonging to the Bombycidæ.
179 [The larvæ of genera 14, Phyciodes, and 35, Crenis, are likewise spiny. See Edwards’ “Butt. of N. Amer.” vol. ii. for figures of the caterpillar of Phyc. Tharos: for notes on the larvæ of Crenis Natalensis and C. Boisduvali see a paper by W. D. Gooch, “Entomologist,” vol. xiv. p. 36. The larvæ of genus 55, Ageronia, are also spiny. (See Burmeister’s figure of A. Arethusa, “Lép. Rép. Arg.” Pl. V. Fig. 4). The larvæ of genus 98, Aganisthos, also appear to be somewhat spiny (see Burmeister’s figure of A. Orion, loc. cit. Pl. V. Fig. 6), and this raises the question as to whether the genus is correctly located in its present position. The larvæ of the following genera figured in Moore’s “Lepidoptera of Ceylon,” parts i. and ii., are all spiny:—6, Cirrochroa (Pl. XXXII.); 7, Cynthia (Pl. XXVI.); 27, Kallima (Pl. XIX.); and 74, Parthenos (Pl. XXIV.). Many species of caterpillars which are spiny when adult appear to be spineless, or only slightly hairy when young. See Edwards’ figures of Melitæa Phaeton, Argynnis Diana, and Phyc. Tharos (loc. cit.) and his description of the larva of Arg. Cybele, “Canad. Entom.” vol. xii. p. 141. The spiny covering thus appears to be a character acquired at a comparatively recent period in the phyletic development. R.M.]
180 [The larvæ of the 110th genus, Paphia, Fabr. (Anæa, Hübn.) are also smoothed-skinned. See Edwards’ figure (loc. cit. vol. i. Pl. XLVI.) of P. Glycerium. Also C. V. Riley’s “Second Annual Report” on the insects of Missouri, 1870, p. 125. Burmeister figures the larva of a species of Prepona (genus 99) which is smooth (P. Demophon, loc. cit. Pl. V. Fig. 1). The horns on the head of Apatura, &c., may possibly be a survival from a former spiny condition. R.M.]
181 “Synopsis of the described Lepidoptera of North America.” Washington, 1862.
182 “Catalog der Lepidopteren des Europäischen Faunengebietes.” Dresden, 1871.
183 This group of moths (“Schwärmer”) is regarded as of very different extents by systematists; when I here comprise under it only the Sphingidæ proper and the Sesiidæ, I by no means ignore the grounds which favour a greater extension of the group; the latter is not rigidly limited. [The affinities of the Sesiidæ (Ægeriidæ) are by no means clearly made out: it appears probable that they are not related to the Sphingidæ. See note 160, p. 370. R.M.]
184 [For Mr. A. G. Butler’s observations on the genus Acronycta, see “Trans. Ent. Soc.” 1879, p. 313; and note 68, p. 169, of the present volume. R.M.]
185 [The following characters are given in Stainton’s “Manual of British Butterflies and Moths,” vol. i. p. 114:—“Larva of very variable form: at one extreme we find the singular Cerura larvæ, with only fourteen legs, and two long projecting tails from the last segment; at the other extreme we have larvæ with sixteen legs and no peculiarity of form, such as Chaonia and Bucephala; most have, however, the peculiarity of holding the hind segment of the body erect when in repose; generally quite naked, though downy in Bucephala and rather hairy in Curtulu; very frequently there are projections on the back of the twelfth segment.” R.M.]
186 Encyl. Meth. ix. p. 310.
187 [The genus Vanessa (in the wide sense) appears to be in a remarkable condition of what may be called phyletic preservation. Thus, the group of species allied to V. C.-album passes by almost insensible steps into the group of butterflies typified by our “Tortoiseshells.” The following is a list of some of the intermediate species in their transitional order:—I.-album, V.-album, Faunus, Comma, California, Dryas, Polychloros, Xanthomelas, Cashmirensis, Urticæ, Milberti, &c. Similarly, our Atalanta and Cardui are connected by a number of intermediate forms, showing a complete transition from the one to the other. The following is the order of the species so far as I am acquainted with them:—Atalanta, Dejeanii, Callirhoë, Tammeamea, Myrinna, Huntera, Terpsichore, Carye, Kershawii, and Cardui. R.M.]
188 “Prodromus Systematis Lepidopterorum.” Regensburg, 1864.
189 [The larva of Acherontia Morta, figured by Butler (see note 121, p. 262), possesses the characteristically recurved horn; that of Ach. Medusa figured by the same author, does not appear to possess this character in any marked degree. R.M.]
191 Loc. cit. Pl. XXV. [This species is referred by Butler to the genus Paonias, Hübn. R.M.]
192 Abbot and Smith, Pl. XXIX. [Placed by Butler in the genus Cressonia, Grote and Robinson. Abbot and Smith state that this larva is sometimes green. According to Mr. Herman Strecker (Lepidop. Rhopal. and Hetero, Reading, Pa. 1874, p. 54) it feeds upon black walnut (Juglans Nigra), hickory (Carya Alba), and ironwood (Ostrya Virginica). Of the North American species of Smerinthus, the following, in addition to Excæcatus, closely resemble our Ocellatus:—S. (Calasymbolus) Geminatus, Say; (C.) Cerisii, Kirby; and Ophthalmicus, Boisd. In addition to S. (Cressonia) Juglandis, S. (Triptogon) Modesta much resembles our Populi. The larva of Geminatus, according to Strecker, is “pale green, lightest above, with yellow lateral granulated stripes; caudal horn violet; stigmata red. It feeds on the willow.” R.M.]
193 Cat. Brit. Mus.
194 [This lengthening of the true legs is mimetic according to Hermann Müller, and causes the anterior portion of the caterpillar to resemble a spider. See note 129, p. 290. R.M.]
195 [Certain butterflies appear to be crepuscular, if not nocturnal in their habits. Thus in his “Notes on the Lepidoptera of Natal,” Mr. W. D. Gooch states that he never saw Melanitis, Leda, or Gnophodes Parmeno on the wing by day, but generally during the hour after sunset. He adds:—“My sugar always attracted them freely, even up to 10 or 11 p.m.” Many species of Hesperidæ are also stated to be of crepuscular habits by this same observer. See “Entomologist,” vol xvi. pp. 38 and 40. R.M.]
196 I only make this assumption for the sake of simplicity, and not because I am convinced that the existing Rhopalocera are actually the oldest Lepidopterous group.
197 Zeitschrift für wissenschaftl. Zoologie, vol. xx. p. 519.
198 [See for instance Lubbock’s “Origin and Metamorphoses of Insects,” chap. iii.; and F. M. Balfour’s “Comparative Embryology,” vol. i., 1880, pp. 327—356. This last work contains an admirable résumé of our knowledge of the embryonic development of insects up to the date of publication. R.M.]
199 Are not the 4th, 11th, and 12th segments destitute of the rudiments of legs as in the larvæ of all existing saw-flies? I might almost infer this from Bütschli’s figures (see for instance Pl. XXV., Fig. 17A).
200 [The grub-formed Hymenopterous larvæ, like the larvæ of all other holometabolous insects, thus represent an acquired degenerative stage in the development, i.e. an adaptation to the conditions of life at that stage. Bearing in mind the above-quoted observations of Bütschli and the caterpillar-like form of the Terebrantiate group of Hymenopterous larvæ, the following remarks of Balfour’s (loc. cit. p. 353), appear highly suggestive:—“While in a general way it is clear that the larval forms of insects cannot be expected to throw much light on the nature of insect ancestors, it does nevertheless appear to me probable that such forms as the caterpillars of the Lepidoptera are not without a meaning in this respect. It is easy to conceive that even a secondary larval form may have been produced by the prolongation of one of the embryonic stages; and the general similarity of a caterpillar to Peripatus, and the retention by it of post-thoracic appendages, are facts which appear to favour this view of the origin of the caterpillar form.” See also Sir John Lubbock, loc. cit., pp. 93 and 95. R.M.]
201 [In the most recent works dealing with this order six groups, based on the character of the imagines are recognized, viz.:—Tubulifera, Terebrantia, Pupivora, Heterogyna Fossores, and Mellifera. (See, for instance, F. P. Pascoe’s “Zoological Classification,” 2nd ed. p. 147.) Of these groups the larvæ of the Terebrantia as thus restricted are all of the caterpillar type (Tenthredinidæ and Siricidæ), whilst those of the other groups are maggot-shaped. For a description of the development of the remarkable aberrant larva of Platygaster, see Ganin in Zeit. f. wissenschaftl. Zool., vol. xix. 1869. R.M.]
202 [For recent investigations on the structure of the thorax in Diptera, see a paper by Mr. A. Hammond, in Journ. Linn. Soc., Zoology, vol xv. p. 9. R.M.]
203 I am familiar with the fact that the two sub-orders of true Diptera, the short-horned (Brachycera), and the long-horned (Nemocera), are not sharply limited; and I am likewise well acquainted with the circumstance that there are forms which connect the two larval types. The connecting forms of the imagines do not, however, always coincide with the intermediate larval forms, so that there here arises a second and very striking incongruence of morphological relationship which depends only upon the circumstance that the one stage has diverged in form more widely than the other through a greater divergence in the conditions of life. The difficulty is in these cases aggravated because an apparent is added to the true form-relationship through convergence, so that without going into exact details the form and genealogical relationships of the Diptera cannot be distinguished. It would be of great interest for other reasons to make this investigation, and I hope to be able to find leisure for this purpose at some future period.
204 “Entwicklung der Dipteren.” Leipzig, 1864.
205 Lubbock concludes from the presence of thoracic legs in the embryonic larva of bees that these have been derived from a larva of the Campodea type, but he overlooks the fact that the rudiments of the abdominal legs are also present; loc. cit., p. 28.
206 “Für Darwin,” Leipzig, 1864, p. 8.
207 Mem. Peabody Acad. of Science, vol. i. No. 3.
208 Verhandl. Wien. Zoolog. Botan. Gesellsch. 1869, p. 310.
209 Über Ontogenie und Phylogenie der Insekten. Eine akademische Preisschrift. Jen. Zeitschrift. Bd. x. Neue Folge, iii. Heft 2. 1876. [Some remarks by F. M. Balfour on the origin of certain larval forms have already been quoted in a previous note (p. 485). This author further states:—“The fact that in a majority of instances it is possible to trace an intimate connection between the surroundings of a larva and its organization proves in the clearest way that the characters of the majority of existing larval forms of insects have owed their origin to secondary adaptations. A few instances will illustrate this point:—In the simplest types of metamorphosis, e.g. those of the Orthoptera genuina, the larva has precisely the same habits as the adult. We find that a caterpillar form is assumed by phytophagous larvæ amongst the Lepidoptera, Hymenoptera, and Coleoptera. Where the larva has not to go in search of its nutriment the grub-like apodous form is assumed. The existence of such an apodous larva is especially striking in the Hymenoptera, in that rudiments of thoracic and abdominal appendages are present in the embryo and disappear again in the larva.... It follows from the above that the development of such forms as the Orthoptera genuina is more primitive than that of the holometabolous forms, &c.” Comparative Embryology, vol. 1, p. 352. R.M.]
210 [The Aphaniptera are now recognized in this country as a sub-order of Diptera. See, for instance, Huxley’s “Anatomy of Invertebrated Animals,” p. 425, and Pascoe’s “Zoological Classification,” 2nd ed. p. 122. R.M.]
211 [This illustration of course only applies to the old arrangement of the Hymenoptera into Terebrantia and Aculeata. See also note 201, p. 488. R.M.]
212 [Eng. ed. This law is perhaps a little too restricted, inasmuch as it is theoretically conceivable that the organism may be able to adapt itself to similar conditions of life in different ways; differences of form could thus depend sometimes upon differences of adaptation and not upon differences in the conditions of life, or, as I have formerly expressed it, it is not necessary to allow always only one best mode of adaptation.]
213 [It must be understood that the word rendered here and elsewhere throughout this work as “transformation” is not to be taken in the narrow sense of metamorphosis, but as having the much broader meaning of a change of any kind incurred by an organism. Metamorphosis is in fact but one phase of transformation. R.M.]
214 By the Editor.
215 Mr. C. V. Riley in his excellent “Annual Reports” already quoted in previous notes, states that the larvæ of Agrotis Inermis, Leucania Unipuncta (Army-worm), and L. Albilinea are all loopers when newly hatched. (See First Report, p. 73; Eighth Report, p. 184; and Ninth Report, p. 53.)
216 The following species not referred to in the previous part of this work are figured by Semper (Beit. zur Entwicklungsgeschichte einiger ostasiat. Schmet.; Verhandl. d. k.k. zoo. bot. Gesell. in Wien, 1867):—Panacra Scapularis, Walk.; Chærocampa Clotho, Drury; and Diludia (Macrosila) Discistriga, Walk. The following are figured by Boisduval and Guenée. (Spéc. Gén. 1874):—Smerinthus Ophthalmicus, Boisd.; Sphinx Jasminearum, Boisd.; S. (Hyloicus) Plebeia, Fabr.; S. (Hyloicus) Cupressi, Boisd.; S. (Pseudosphinx) Catalpæ, Boisd.; Philampelus Jussiuæ, Hübn. (= Sphinx Vitis, Linn.?); and Ceratomia Amyntor, Hübn. As the works of Abbot and Smith, and Horsfield and Moore have been exhausted by Dr. Weismann, it is quite unnecessary to extend this note by giving a list of the species figured by these authors.
217 The same inference has already been drawn with respect to Pterogon (Proserpinus) Œnotheræ, see pp. 257, 258.
218 This would of course be the fourth segment if the head be considered the first, as on the Continent.
219 “Second Annual Report,” 1870, p. 78.
220 “Entomologist,” vol. xiv. p. 7.
221 With reference to the habits of C. Capensis (p. 531), I have since been informed by Mr. Trimen that this species does not conceal itself by day, so that the dimorphism may be regarded as a character retained from an earlier period and adapted to the present life conditions.
222 “Kosmos,” Dec. 1877, p. 218. The paper is here introduced chiefly with a view to illustrate an important case of incongruence among Lepidopterous pupæ.
223 [Maracujá, the local name for the Passiflora. R.M.]
225 Verhandl. Schweiz. Naturforsch. Gesellschaft. Einsiedeln, 1868.