Studies in the Theory of Descent, Volume II

That this secondary variability is to a certain extent brought about by the conflict between the old and new characters, the latter striving to suppress the former, is shown by the caterpillar of Saturnia Carpini which I have observed for many years from this point of view, and than which I do not know a more beautiful illustration.

When these larvæ leave the egg they are black, but in the adult state are almost bright green – this at least being the case in a local form which, from the district in the vicinity of Genoa where it is found, I will designate as the var. Ligurica. Now whilst these two extreme stages of development are relatively constant, the intermediate stages show a variability which becomes greater the nearer the last stage is approached, this variation in the marking depending simply on the struggle between the green colour and the more anciently inherited black. In this manner there arises, especially in the fourth stage of the German local form, an incredible mixture of the most diverse markings, all of which can, however, be very easily explained from the foregoing point of view.

The simpler and, as I am inclined to believe, the older form of the transformation is presented to us in the local variety Ligurica. In the last stage, when 7.5 centimeters long, this form is of a beautiful bright green colour without any trace of black marking[4 - 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.] (Pl. VIII (#Plate_VIII)., Fig. 77). The colour of the six orange warts which are situated on each segment is also similar in all specimens, so that this stage is perfectly constant.

Our German S. Carpini shows different characters in the fifth stage. It is true that individual specimens occur which are entirely green without any black, but these are rare; the majority possess a more or less broad black ring encircling the middle of each segment (Pl. VIII (#Plate_VIII)., Figs. 78 and 79). Those specimens in which the black ring has become broken up into large or small spots surrounding the base of the warts constitute intermediate forms (Fig. 80 (#Plate_VIII)). The last stage of the German local form, unlike that of the Genoese local form, is therefore very variable.

The two forms, moreover, do not simply differ in being more or less advanced in phyletic development, but also in several other points. As it is of great theoretical interest to show that a species can develop local differences only in the stage of larva, I will here subjoin the plain facts.

The differences consist in that the Genoese local form goes through five moults whilst the German local form, like most caterpillars, has only four moults. Further, in the Genoese form the light green, which is also possessed by the German form in the fourth stage, when it once appears, is retained to the end of the larval development, whilst in the fifth stage of the German form this colour is replaced by a dull greyish-green (compare Figs. 77 and 78 (#Plate_VIII)). There is further a very considerable difference in the earlier stages which shows that the phyletic transforming process has taken a quite independent course in the two forms. Since the struggle between the green and black – retaining this idea – appears to be quite finished in the last stage of the Genoese form, we should expect that the new colour, green, would now also have encroached further upon the younger stages than in the German form. Nevertheless, this is not the case, but quite the reverse happens, the black maintaining its ground longer in the Italian than in the German form.

In the Genoese form the two first stages are completely black, and in the third stage an orange-yellow lateral stripe first appears. In the German form this stripe appears in the second stage, and there is not subsequently added, at least on the middle segments, a yellow border surrounding some of the warts of the median series. In the third stage, however, the yellow (which is but the precursor of the later green colour) becomes further extended, so that the caterpillars often appear of an orange colour, some or all of the warts and certain spots and stripes only being black (Figs. 66 and 68 (#Plate_VII)). The warts are also often yellow while the ground remains in most part black – in brief, the bright colour is in full struggle with the black, and an endless series of variations is the result of this conflict, whilst in the corresponding stage of the Genoese form almost complete constancy prevails.

This constancy remains also in the following (fourth) stage, the caterpillar still being deep black, only the yellow (sulphur-coloured) lateral stripe, which has now become brighter, indicating the impending change (Fig. 67 (#Plate_VII)). This takes place in the fifth stage, in which the ground-colour suddenly becomes bright green, the black remaining at most only in traces on the anterior edges of the segments.

This is the same marking as is shown by the fourth stage of the German form, only in this case individuals quite destitute of black do not occur. In many specimens indeed black forms the ground-colour, the green only appearing in certain spots (Figs. 71 to 75 (#Plate_VIII)); in others the green predominates, and these two extremes are connected by innumerable intermediate forms, so that this stage must be regarded as the most variable of all.

The sixth stage of the Genoese and the fifth of the German form have already been compared together. The results may be thus tabulated: —

A. German form.B. Genoese form.

Stage I. 9 days. Black; constant. 9 days. Black; constant.

Stage II. 8 days. Black, with orange-yellow lateral stripe; variable. Black, with yellow; very variable. 11 days. Black; constant.

Stage III. 5 days (in some cases as much as 16 days). 12 days. Black, with orange-yellow lateral stripes; constant.

Stage IV. 16 days (in some cases only 5 days). Bright green and black mixed; very variable. 6 days. Black, with bright yellowish lateral stripe; constant.

Stage V. 6 days (frequently longer). Dark green, with or without black bands; variable. 6 days. Bright green, small traces of black; variable.

Stage VI. Pupation. 18 days. Bright green, without any black; constant.

Stage VII. Pupation.

From this comparison we perceive that the process of transformation has at least become preliminarily concluded in the Genoese form. Why the backward transference of the newly-acquired character to the young stages has not yet occurred, or, at least, why it is not in progress, does not appear; neither can it be stated whether this will take place later, although we may venture to suppose that such will be the case. At first sight but a relatively short time appears necessary for the single stage V., which is still in a state of fluctuation (variable), to become constant by continued crossing, like all the other stages.

That the transformation is still in full progress in the German form, is shown by the fact that in this case all the stages are variable with the exception of the first – the second stage being only variable to a small extent, the third to a much greater extent, and the fourth to the highest degree conceivable, whilst the fifth and last stage is again less variable – so that the greatest struggle between the old and new characters takes place in the fourth stage.

Among the innumerable variations presented by this last stage a complete series of transitional forms can be arranged so as to show the gradual conquest of the black by the green, and thus indicating, step by step, the course which the latter colour has taken.

In the blackest specimens there is nothing green but the lateral (infra-spiracular) line which was yellow in the preceding stage, and a crescent-shaped streak at the base of the middle warts together with a still smaller crescent at the base of the upper warts (Figs. 71 and 81 (#Plate_VIII)). These spots become extended in lighter specimens and approximate so as to leave only narrow black bridges, a third spot being added at the posterior edge of the warts (Figs. 72 and 82 (#Plate_VIII)). The three spots then extend on all sides, still leaving for a long period narrow black lines at the boundaries where their growth has caused them to abut. In this manner there frequently arises on the green ground a true hieroglyphic-like marking (Figs. 85 and 86 (#Plate_VIII)). Finally the black disappears from the anterior edge and diminishes on the middle line of the back where it still partly remains as a T-shaped figure (Figs. 73 and 74 (#Plate_VIII)), although generally replaced elsewhere by the green with the exception of small residues.

One point remained for a long time inexplicable to me, viz., the change of the light green into dark grey-green which appeared in the last stage in connection with a total change of the black marking.

Supposing that new characters are actually acquired only in the last stage, and that from this they are transferred to the younger stages, we should expect to find completely developed in the last stage the same colouring and markings as are possessed more or less incompletely in the fourth stage. Now since the developmental tendency to the removal of black and to the predominance of green – if we may thus venture to express it – is obvious in the fourth stage, we may expect to find in the fifth stage a bright green ground-colour, either without any mixture of black or with such black spots and streaks as were retained in the fourth stage as residues of the original ground-colour. But instead of this the fifth stage shows a dark green colour, and a more or less developed black marking which cannot in any way be derived from that of the fourth stage.

The Genoese local form observed last year first gave me an explanation to the extent that in this form the last stage is actually only the potential penultimate stage, or, more correctly expressed, that the same characters which at present distinguish the last stage of this form, are already more or less completely transferred to the penultimate stage.

The apparently paradoxical behaviour of the German form can be explained by supposing that before the pure bright green had become completely transferred to the penultimate stage a further change appeared in the last stage, the green ground-colour becoming darker, and black transverse bands being formed. The marking of the last stage would then be regarded as the reverse of that of the preceding stage; the absence of black would be the older, simple black spots at the base of the warts the next in succession, and a connected black transverse band the most advanced state of the development.

Whether this explanation is correct, and if so, what causes have produced the second change, may perhaps be learnt at some future time by a comparison with the ontogeny of other Saturniidæ; in the meantime this explanation receives support from another side by the behaviour of the Genoese local form. If the last stage of the German form has actually commenced to be again re-modelled, then this variety is further advanced in phyletic development than the Genoese form; and this corresponds entirely with the theory that in the former the light colour (the orange considered as preliminary to the transformation into green) has already been carried down into the second stage, whilst in the Genoese variety even in the fourth stage only the first rudiments of the colour-transformation show themselves.

The Genoese form is to a certain extent intermediate between the German form of Saturnia Carpini and the nearly related S. Spini, a species inhabiting East Germany. In this latter the larvæ, even in the adult state, are completely black with yellow warts. This form of caterpillar must therefore be regarded as phyletically the oldest, and this very well agrees with the character of the moth, which differs essentially from S. Carpini only in not being sexually dimorphic. In Carpini the male possesses a far more brilliant colouring than the female, the latter agreeing so completely with the female of Spini that it can hardly be distinguished therefrom, especially in the case of the somewhat larger South European specimens of the last species. Now as the more simple colouring of the female must in any case be regarded as the original form, we must consider Spini, both sexes of which possess this colouring, to be phyletically the older form, and Carpini, the male of which has become differently coloured, must be considered as the younger type. This completely accords with the characters of the larvæ.

I must here mention that I have also asked myself the question whether the variations of the different larval stages are connected together as cause and effect – whether the lightest specimens of the fifth stage may perhaps not also have been the lightest individuals of the third and fourth stages.

Such relationship is only apparent between the third and fourth stages; the darkest larvæ of the third stage become the darker varieties of the fourth stage, although it is true that the lighter forms of the third sometimes also become dark varieties in the fourth stage. Between the fourth and fifth stages there is scarcely any connection of this kind to be recognized. Thus, the darkest varieties of the fourth stage sometimes become the lightest forms of the fifth stage, whilst in other cases from the lightest individuals of the fourth stage there arise all the possible modifications of the fifth stage. Further details may be omitted: the negative result cannot cause any surprise, as it is a necessary consequence of the continued crossing that must take place.

We thus see that the three chief stages of development (larva, pupa, and imago) actually change in colour independently of each other, the single stages of the larval development being however in greater dependence upon one another, and being connected indeed in such a manner that a new character cannot be added to the last stage without being transferred in the course of time to the preceding stage, and at a later period from this again even to the youngest stage, supposing it not to be previously delayed in the course of its transference by unknown opposing forces. On this last point, however, the facts at present available do not admit of any certain decision.

But why do the individual larval stages behave in this respect so very differently to the chief stages of the whole development? why are the former so exactly correlated whilst the latter are not? If new characters have a general tendency to become transferred to the younger ontogenetic stages, why are not new imaginal characters first transferred to the pupa, and finally to the larva?

The answer to these questions is not far to find. The wider two stages of a species differ in structure, the less does correlation become possible; the nearer the two stages are morphologically related, the more powerful does the action of correlation become. It is readily conceivable that the more widely two succeeding stages deviate in structure and mode of life, the less possible does it become for characters to be transferred from one to the other. How is it possible, for example, that a new character in the proboscis or on the wings of a butterfly can be transferred to the caterpillar? If such correlation existed it could only manifest itself by some other part of the caterpillar changing in correspondence with the change of the proboscis or wings of the butterfly. That this is not the case has, in my opinion, been conclusively shown by all the foregoing considerations respecting the independent variability of the chief stages of the metamorphosis.

There are, moreover, an endless number of facts which prove the independence of the individual stages of development – I refer to the multitudinous phenomena presented by metamorphosis itself. The existence of that form of development which we designate as metamorphosis is alone sufficient to prove incontestably that the single stages are able to change independently of one another to a most remarkable extent.

If we now ask the question: how has the so-called “complete” metamorphosis of insects arisen? the answer can only be: through the gradual adaptation of the different stages of development to conditions of life which have continually deviated more and more widely from each other.[5 - 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.]

But if individual stages of the post-embryonic development can finally attain to such complete diversity of structure as that of the larva and imago through gradual adaptations to continually diverging conditions of life, this shows that the characters acquired by the single stages are always only transferred to the same stages of the following generation, whilst the other stages remain uninfluenced thereby. This depends upon that form of heredity designated by Darwin “inheritance at corresponding periods of life,” and by Haeckel “homochronic heredity.”

II. Does the Form-relationship of the Larva coincide with that of the Imago?

Having thus established the independence in the variability of the individual stages of metamorphosis, I will now turn to the consideration of the question as to how far a parallelism is displayed in the phyletic development of these stages. Is there a complete congruence of form-relationship between larvæ on the one hand and imagines on the other? does the classification founded on the morphology of the imagines agree with that based on the morphology of the larvæ or not?

If, according to Claus,[6 - “Grundzüge der Zoologie,” 1875.] we divide the order Lepidoptera into six great groups of families, it is at once seen that these groups, which were originally founded exclusively on imaginal characters, cannot by any means be so clearly and sharply defined by the larval characters.

This is certainly the case with the Geometræ, of which the larvæ possess only ten legs, and on this account progress with that peculiar “looping” movement which strikes even the uninitiated. This group, which is very small, is however the only one which can be founded on the morphology of the larvæ; it comprises only two nearly related families (Phytometridæ and Dendrometridæ), and it is not yet decided whether these should not be united into one group comprising the family characters of the whole of the “loopers.”

Neither the group of Micro-lepidoptera, nor those of the Noctuina, Bombycina, Sphingina, and Rhopalocera, can be based systematically on larval characters. Several of these groups are indeed but indistinctly defined, and even the imagines present no common characteristics by which the groups can be sharply distinguished.

This is well shown by the Rhopalocera or butterflies. These insects, in their large and generally brilliantly coloured wings, which are usually held erect when at rest, and in their clubbed antennæ, possess characters which are nowhere else found associated together, and which thus serve to constitute them a sharply defined group.[7 - [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.]] The caterpillars, however, show a quite different state of affairs. Although the larval structure is so characteristic in the individual families of butterflies, these “larval-families” cannot be united into a larger group by any common characters, and the “Rhopalocera” would never have been established if only the larvæ had been known. It is true that they all have sixteen legs, that they never possess a Sphinx-like horn, and that they are seldom hairy, as is the case with many Bombycidæ,[8 - The genus of Morphinæ, Discophora, possesses hairs very similar to those of the genus Cnethocampa belonging to the Bombycidæ.] but these common negative characters occur also in quite distinct groups.

In the butterflies, therefore, a perfect congruence of form-relationship does not exist, inasmuch as the imagines constitute one large group of higher order whilst the larvæ can only be formed into families. If it be admitted that the common characters of butterflies depend on their derivation from a common ancestor, the imagines must have retained certain common characters which enable them to be recognized as allies, whilst the larvæ have preserved no such characters from the period at which the families diverged.

Without going at present into the causes of these phenomena I will pass on to the consideration of further facts, and will now proceed to investigate both the form-relationships within the families. Here there can be no doubt that in an overwhelmingly large majority of cases the phyletic development has proceeded with very close parallelism in both stages; larval and imaginal families agree almost completely.

Thus, under the group Rhopalocera there is a series of families which equally well permit of their being founded on the structure of the larva or on that of the imago, and in which the larvæ and imagines therefore deviate from one another to the same extent. This is the case, for instance, with the families of the Pieridæ, Papilionidæ, Danaidæ, and Lycænidæ.

But there are also families of which the limits would be very different if the larvæ were made the basis of the classification instead of the butterflies as heretofore. To this category belongs the sub-family Nymphalinæ. Here also a very characteristic form of caterpillar indeed prevails, but it does not occur in all the genera, being replaced in some by a quite different form of larva.

In the latest catalogue of Diurnal Lepidoptera, that of Kirby (1871), 112 genera are comprised under this family. Of these most of the larvæ possess one or several rows of spines on most or on all the segments, a character which, as thus disposed, is not met with in any other family.

This character is noticeable in genera 1 to 90, if, from those genera of which the larvæ are known, we may draw a conclusion with reference to their allies. I am acquainted with larvæ of genus 2, Agraulis, Boisd. (Dione, Hübn.); of genus 3, Cethosia, Fabr.; 10, Atella, Doubl.; 12, Argynnis, Fabr.; 13, Melitæa,[9 - [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.]] Fabr.; 19, Araschnia, Hübn.; 22, Vanessa, Fabr.; 23, Pyrameis, Hübn.; 24, Junonia, Hübn.; 31, Ergolis, Boisd.; 65, Hypolimnas, Hübn. (Diadema, Boisd.); 77, Limenitis, Fabr.; 81, Neptis, Fabr.; 82, Athyma, Westw.; and finally with those of genus 90, Euthalia, Hübn. – which, according to Horsfield’s figures, possess only two rows of spines, these being remarkably long and curved, and fringing both sides. It may be safely assumed that the intermediate genera would agree in possessing this important character of the Nymphalideous larvæ, viz., spines.

After the genus 90 there are 22 more genera, and these are spineless, at least in the case of the two chief genera, 93, Apatura, and 104, Nymphalis. Of the remainder I know neither figures nor descriptions.[10 - [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.]] In the two genera named the larvæ are provided with two or more spine-like tentacles on the head, and the last segment ends in a fork-like process directed backwards. The body is otherwise smooth, and differs also in form from that of the larvæ of the other Nymphalinæ, being thickest in the middle, and tapering anteriorly and posteriorly; neither is the form cylindrical, but somewhat flattened and slug-shaped. If therefore we were to arrange these butterflies by the larvæ instead of by the imagines, these two genera and their allies would form a distinct family, and could not remain associated with the 90 other Nymphalideous genera.

We have here a case of incongruence; the imagines of the genera 1–90 and 91–112 are more closely allied than their larvæ.