The existence of a whole series of species of Amblystoma, as already mentioned, at once shows that species of Siredon can become elevated into the salamander form, and can propagate regularly in this state, and further, that this phyletic advance has already actually taken place in many species.
That degeneration may also occur from this high stage to a lower stage of development, is shown by many observations on our water-salamanders. It is known that under certain circumstances Tritons, as it is generally expressed, become “sexually mature in the larval condition.”
In the year 1864 De Filippi[244] found fifty Tritons in a pool at Andermatten, in the neighbourhood of Puneigen, and of these only two showed the structure of the adult water-salamander; all the others still possessed gills, but notwithstanding this, they agreed in both sexes, in size and in the development of the sexual organs, with mature animals. De Filippi established that these “sexually mature larvæ” not only resembled larvæ externally through the possession of gills, but that they also possessed all the other anatomical characters of the larvæ, i.e. the characteristic bunches of palatine teeth situated on both sides in the position of the subsequent single rows, and a vertebral column represented throughout its whole length by the chorda dorsalis.
According to my view this would be a case of the reversion of the Triton to the immediately anterior phyletic stage, i.e. to the perennibranchiate stage, and in the present instance the majority of zoologists who take their stand by the theory of descent, would certainly concur in this view. I should at least consider it to be a useless play upon words did we here speak of larval reproduction, and thereby believe that we had explained something. The animal certainly becomes sexually mature in the same condition as that in which it first appears as a larva, but we first get an insight into the nature of this process by considering that this so-called “sexually mature larva” has the precise structure which must have been possessed by the preceding phyletic stage of the species, and that an individual reversion to the older phyletic stage of the species is consequently before us. I maintain that Duméril is in error in regarding this case of the Triton as parallel with the true larval reproduction of Wagner’s Cecidomyia larva. In this last case it is certainly not reversion to an older phyletic stage that confers the power of reproduction upon the larvæ, since the latter do not represent an older phyletic stage of the species, but must have arisen contemporaneously with this last stage. The enormous structural difference between the larvæ and the imagines is not explained by the latter having arisen from the former supplementarily as a finished production, but by both having been contemporaneously adapted to continually diverging conditions of life.[245] Considered phyletically, these larvæ are by no means necessarily transitional to the origination of the flies. They could have been quite different without the form of the imagines having been thereby modified, since the stages of insect metamorphosis vary independently of each other in accordance with the conditions of life to which they are subjected, and exert scarcely any, or only a very small form-determining influence upon each other, as has been amply proved in the preceding essay. In any case the power of these larvæ (the Cecidomyiæ) to propagate themselves asexually was first acquired as a secondary character, as appears from the fact that there exist numerous species of the same genus which do not “nurse.” In the form which they now possess they could never have played the part of the final stage of the ontogeny, nor could they formerly have possessed the power of sexual reproduction.[246] In brief, we are here concerned with true larval reproduction, whilst in Triton we have reversion to an older phyletic stage.[247]
I cannot agree with my friend Professor Haeckel when he occasionally designates the reversion of the Tritons as an “adaptation” to a purely aqueous existence.[248] We could here only speak of “adaptation” if we took the word in a quite different sense to that in which it was first introduced into science by Darwin and Wallace. These naturalists thereby designate a gradual bodily transformation appearing in the course of generations in correspondence with the new requirements of altered conditions of life or, in other words, the action of natural selection, and not the result of a suddenly and direct acting transforming cause exerted but once on a generation.
Just because the word “adaptation” can be used in ordinary language in many senses, it is desirable that it should have only one precise signification, and above all that we should not speak of adaptation where scarcely any morphological change occurs, but only a kind of functional change in the sense used by Dohrn.[249] This is the case for example, when Forel[250] shows that fresh water Pulmonifera, the organization of which is attributed to the direct respiration of air, can nevertheless become settled in the greatest depths of mountain lakes through their lungs being again employed as gills. That not the least change in the lungs hereby takes place is shown by the observations of Von Siebold,[251] who saw the shallow water Pulmonifera using their lungs alternately for direct aërial and aquatic respiration, according to the amount of air contained in the water. If with Von Siebold we merely apply the word “adaptation” to such cases, this expression would lose the special sense which it originally conveyed, and the word would have to be abandoned as a terminus technicus; still, such cases may perhaps be spoken of as physiological adaptation.
In any case the reproductive “larvæ” of the Tritons as little present a case of true adaptation as the Axolotl, which occasionally becomes transformed into an Amblystoma. In both cases the transformation referred to is by no means indispensable to the life of the individual. Mature Tritons (devoid of gills) can exist, as I have myself seen, for many months, and probably also for a year in deep water, although adapted for purely pulmonary respiration; whilst Axolotls, as I have already mentioned, can live well for a year in shallow water poor in air. If their gills by this means become shrivelled up or completely disappear, even this is not adaptation in the Darwinian sense, but the effect of directly acting external influences, and chiefly of diminished use.
A case entirely analagous to that of Filippi’s was observed by Jullien in 1869. Four female larvæ of Lissotriton Punctatus (Bell)—(synonymous with Triton Tæniatus, Schnd.), taken from a pool, proved to be sexually mature. They contained mature eggs in their ovaria ready for laying, and two of them actually deposited eggs. Four male larvæ found in the same pool, appeared to be equally developed with respect to size, but their testicles contained no free spermatozoa, but only sperm-cells.[252]