In the same way it has been recently supposed that those extinct flying saurians, the pterodactyles, had an affinity with birds more marked than any other known animals. Now, however, as has been said earlier, it is contended that not only had they no such close affinity, but that other extinct reptiles had a far closer one.
The amphibia (i.e. frogs, toads, and efts) were long considered (and are so still by some) to be reptiles, showing an affinity to fishes. It now appears that they form with the latter one great group—the ichthyopsida of Professor Huxley—which differs widely from reptiles; while its two component classes (fishes and amphibians) are difficult to separate from each other in a thoroughly satisfactory manner.
If we admit the hypothesis of gradual and minute modification, the succession of organisms on this planet must have been a progress from the more general to the more special, and no doubt this has been the case in the majority of instances. Yet it cannot be denied that some of the most recently formed fossils show a structure singularly more generalized than any exhibited by older forms; while others are more specialized than are any allied creatures of the existing creation.
A notable example of the former circumstance is offered by macrauchenia—a hoofed animal, which was at first supposed to be a kind of great llama (whence its name)—the llama being a ruminant, which, like all the rest, has two toes to each foot. Now hoofed animals are divisible into two very distinct series, according as the number of functional toes on each hind foot is odd or even. And many other characters are found to go with this obvious one. Even the very earliest Ungulata show this distinction, which is completely developed and marked even in the Eocene palæotherium and anoplotherium found in Paris by Cuvier. The former of these has the toes odd (perissodactyle), the other has them even (artiodactyle).
Now, the macrauchenia, from the first relics of it which were
found, was thought to belong, as has been said, to the even-toed division. Subsequent discoveries, however, seemed to give it an equal claim to rank amongst the perissodactyle forms. Others again inclined the balance of probability towards the artiodactyle. Finally, it appears that this very recently extinct beast presents a highly generalized type of structure, uniting in one organic form both artiodactyle and perissodactyle characters, and that in a manner not similarly found in any other known creature living, or fossil. At the same time the differentiation of artiodactyle and perissodactyle forms existed as long ago as in the period of the Eocene ungulata, and that in a marked degree, as has been before observed.
Again, no armadillo now living presents nearly so remarkable a speciality of structure as was possessed by the extinct glyptodon. In that singular animal the spinal column had most of its joints fused together, forming a rigid cylindrical rod, a modification, as far as yet known, absolutely peculiar to it.
In a similar way the extinct machairodus, or sabre-toothed tiger, is characterized by a more highly differentiated and specially carnivorous dentition than is shown by any predacious beast of
the present day. The specialization is of this kind. The grinding teeth (or molars) of beasts are divided into premolars and true molars. The premolars are molars which have deciduous vertical predecessors (or milk teeth), and any which are in front of such, i.e. between such and the canine tooth. The true molars are those placed behind the molars having deciduous vertical predecessors. Now, as a dentition becomes more distinctly carnivorous, so the hindmost molars and the foremost premolars disappear. In the existing cats this process is carried so far that in the upper jaw only one true molar is left on each side. In the machairodus there is no upper true molar at all, while the premolars are reduced to two, there being only these two teeth above, on each side, behind the canine.