The argument, as we have seen in a previous chapter, for the animal nature of Eozoon depends on our assuming certain parts of this fixity. We suppose that then as now calcium carbonate had been selected as the material for the skeletons of such creatures; that then, as now, minute tubuli and large canals were necessary to enable the soft animal matter to permeate and pass through the skeleton, and that the protoplasmic animal matter of these far back geological periods had the same vital properties of contraction and extension, digestion, etc., that it has to-day. Could any one prove that these determinations of vital and other forces had not been established, or that living protoplasmic matter, with all its wonderful properties, had not been constructed in the Laurentian period, the existence of this ancient animal would be impossible. Yet how much is implied in all this, and though nothing is more unstable chemically or vitally than protoplasm, if it were introduced in the Laurentian, it has continued practically unchanged up to the present time.
If we pass on to the undoubted and varied life of the Cambrian period, we shall find that multitudes of things which might have been otherwise were already settled in a way that has required no change.
In the oldest Trilobites the whole of the mechanical conditions of an external articulated skeleton had been finally settled. The material chitinous or partly calcareous, its microscopic structure, fitted to combine lightness and strength with facility for rapid growth, the subdivision of its several rings, so as to form a protective armour and a mobile skeleton, the arrangement of its spines for defence without interfering with locomotion, the contrivance of hinge joints arranged in different planes in the limbs, all these were already in full perfection, and just as they are found to-day in the skeleton of a king-crab or any other Crustacean. They have, it is true, been modified into a vast number of subordinate forms and uses, but the general principles and main structures all stand. I was much struck with this recently in studying a remarkable specimen now in the National Museum at Washington. It is a large species of Asaphus; the same genus which gave to the late Mr. Billings the limbs of a Trilobite, the first ever described; but in the Washington specimen they are remarkably perfect. Each limb presents a series of joints resembling those of the tarsus of an insect, each joint being of conical form with the narrow proximal end articulated to the enlarged distal end of the previous one, so as to give great facility of movement and accommodation for delicate muscular bands. This tells us of muscular fibre and tendon fitted for flexing and extending these numerous joints, of motor nerves to work that marvellous contractile power of the striated muscle, whose mode of action is still an insoluble mystery, yet one practically solved in the remote Cambrian age for the benefit of these humble inhabitants of the sea. If we could imagine that the inventive power to perfect such machinery was present in the brains of these old Crustaceans or Arachnidans, we might wish that some of them had survived to instruct us in matters which baffle our research.
It is long since the compound eyes of these Trilobites, as illustrated by Burmeister, gave Buckland the opportunity to infer that the laws of light and of vision were the same from the first as now. But what does this imply? Not only that the light of the sun penetrating to the depths of the Cambrian sea, was regulated by the same laws as to-day, but that a series of cameras was perfected to receive the light as reflected from objects, to picture the appearance of these objects on a retinal screen as sensitive as the film of the photographer, and thereby to produce true perceptions of vision in the sensorium of these ancient animals. I have before me a fragment of the eye of a Trilobite (Phacops), in which may be seen the little radiating tubes provided for the several ocelli of the compound eye, just as we see in the modern Limulus; and each of these ocelli must have been a perfect photographic camera, and more than this, since absolutely automatic, and probably having the power to represent colour as well as light and shade. We know also, from the recent experiments of an Austrian physiologist on the eyes of insects, that such compound eyes are so constructed as to present a single picture, just as we can see the whole landscape in looking through the many little panes of a cottage window. In our own time the king-crab and lobster no doubt see just as their predecessors did millions of years ago, and with precisely similar instruments.
But the eyes of the modern Crustaceans have to compete with eyes of a dissimilar type, constructed on the same general optical principles, but quite different in detail. These are the simple or single eyes of the cuttle-fishes and the true fishes. The same rivalry existed in the oldest seas, when the competition of Crustaceans and cuttles was just as keen as now. Though the eyes of the latter have not been preserved, or at least have not yet been found, we have a right to infer that the cuttles of the Cambrian and Silurian seas must have been able to see as well as their Crustacean foes and competitors. If so, the other type of eye must have been perfected for aquatic vision as early as the compound type. In any case we know that a little later, in the Carboniferous period, we have evidence that the eyes of fishes conformed to those of their modern successors. I have myself described[152] a carboniferous fish (Palæoniscus) from the bituminous shales of Albert County, New Brunswick, in which the hard globular lens of the eye had been sufficiently firm and durable to retain its form, and to be replaced by calcite, showing even that like the lens of the eye of a modern fish it had been constructed of concentric laminæ. In the Carboniferous period also, both types of eye, the compound and the single, experienced the further modifications necessary to fit them for vision in air, the compound eye in insects, the simple eye in Batrachians.[153] The original photographic cameras, strange though this may appear to us, were intended for use under water; but at a very early time they were adapted to work in air.
[152] Canadian Naturalist.
[153] See ante, chapter on Air-breathers.
But we must bear in mind that this early solving of advanced problems in mechanics, optics and physiology was in favour of Crustaceans and cuttles, which were lords of creation in their time. There were in those early days humbler creatures whose structures also present wonderful contrivances.
I have already referred, in the chapter on imperfection of the geological record, to the fossil sponges which have been found in so great number and perfection in some of the oldest rocks of Canada, and which have for the first time enabled us to appreciate the forms and structures of the wonderful silicious sponges which preceded those with which the dredgings of the Challenger have made us familiar in the modern seas. Humble sarcodous animals, without distinct muscular or nervous system or external senses, the sponges have at least to live and grow, and to that end they must already, in the dawn of life on our planet,[154] have perfected those arrangements of ciliated cells in chambers and canals which the microscope shows us driving currents of water through the modern sponges, and thereby bringing to them the materials of food and means of respiration. It is true we know as little as the sponges themselves of the modus operandi of those perpetually waving threads which we call cilia or flagella, yet they must have existed with all their powers even before the Cambrian period.[155]