Autobiography and Selected Essays
Chapter 11
What justification is there, then, for the assumption of the existence in the living matter of a something which has no representative, or correlative, in the not living matter which gave rise to it? What better philosophical status has "vitality" than "aquosity"? And why should "vitality" hope for a better fate than the other "itys" which have disappeared since Martinus Scriblerus [107] accounted for the operation of the meat-jack [108] by its inherent "meat-roasting quality," and scorned the "materialism" of those who explained the turning of the spit by a certain mechanism worked by the draught of the chimney.
If scientific language is to possess a definite and constant signification whenever it is employed, it seems to me that we are logically bound to apply to the protoplasm, or physical basis of life, the same conceptions as those which are held to be legitimate elsewhere. If the phaenomena exhibited by water are its properties, so are those presented by protoplasm, living or dead, its properties.
If the properties of water may be properly said to result from the nature and disposition of its component molecules, I can find no intelligible ground for refusing to say that the properties of protoplasm result from the nature and disposition of its molecules.
But I bid you beware that, in accepting these conclusions, you are placing your feet on the first rung of a ladder which, in most people's estimation, is the reverse of Jacob's, and leads to the antipodes of heaven. It may seem a small thing to admit that the dull vital actions of a fungus, or a foraminifer, are the properties of their protoplasm, and are the direct results of the nature of the matter of which they are composed. But if, as I have endeavoured to prove to you, their protoplasm is essentially identical with, and most readily converted into, that of any animal, I can discover no logical halting-place between the admission that such is the case, and the further concession that all vital action may, with equal propriety, be said to be the result of the molecular forces of the protoplasm which displays it. And if so, it must be true, in the same sense and to the same extent, that the thoughts to which I am now giving utterance, and your thoughts regarding them, are the expression of molecular changes in that matter of life which is the source of our other vital phaenomena.[109]
ON CORAL AND CORAL REEFS [110]
The marine productions which are commonly known by the names of "Corals" and "Corallines," were thought by the ancients to be sea-weeds, which had the singular property of becoming hard and solid, when they were fished up from their native depths and came into contact with the air.
"Sic et curalium, quo primum contigit auras Tempore durescit: mollis fuit herba sub undis,"[111]
says Ovid (Metam. xv); and it was not until the seventeenth century that Boccone [112] was emboldened, by personal experience of the facts, to declare that the holders of this belief were no better than "idiots," who had been misled by the softness of the outer coat of the living red coral to imagine that it was soft all through.
Messer Boccone's strong epithet is probably undeserved, as the notion he controverts, in all likelihood, arose merely from the misinterpretation of the strictly true statement which any coral fisherman would make to a curious inquirer; namely, that the outside coat of the red coral is quite soft when it is taken out of the sea. At any rate, he did good service by eliminating this much error from the current notions about coral. But the belief that corals are plants remained, not only in the popular, but in the scientific mind; and it received what appeared to be a striking confirmation from the researches of Marsigli [113] in 1706. For this naturalist, having the opportunity of observing freshly-taken red coral, saw that its branches were beset with what looked like delicate and beautiful flowers each having eight petals. It was true that these "flowers" could protrude and retract themselves, but their motions were hardly more extensive, or more varied, than those of the leaves of the sensitive plant; and therefore they could not be held to militate against the conclusion so strongly suggested by their form and their grouping upon the branches of a tree-like structure.
Twenty years later, a pupil of Marsigli, the young Marseilles physician, Peyssonel, conceived the desire to study these singular sea-plants, and was sent by the French Government on a mission to the Mediterranean for that purpose. The pupil undertook the investigation full of confidence in the ideas of his master, but being able to see and think for himself, he soon discovered that those ideas by no means altogether corresponded with reality. In an essay entitled "Traite du Corail," which was communicated to the French Academy of Science, but which has never been published, Peyssonel writes:--
"Je fis fleurir le corail dans des vases pleins d'eau de mer, et j'observai que ce que nous croyons etre la fleur de cette pretendue plante n'etait au vrai, qu'un insecte semblable a une petite Ortie ou Poulpe. J'avais le plaisir de voir remuer les pattes, ou pieds, de cette Ortie, et ayant mis le vase plein d'eau ou le corail etait a une douce chaleur aupres du feu, tous les petits insectes s'epanouirent.--L'Ortie sortie etend les pieds, et forme ce que M. de Marsigli et moi avions pris pour les petales de la fleur. Le calice de cette pretendue fleur est le corps meme de l'animal avance et sorti hors de la cellule."*[114]
* This extract from Peyssonel's manuscript is given by M. Lacaze Duthiers in his valuable Histoire Naturelle du Corail (1866).
The comparison of the flowers of the coral to a "petite ortie," or "little nettle," is perfectly just, but needs explanation. "Ortie de mer," or "sea-nettle," is, in fact, the French appellation for our "sea-anemone," a creature with which everybody, since the great aquarium mania, must have become familiar, even to the limits of boredom. In 1710, the great naturalist, Reaumur,[115] had written a memoir for the express purpose of demonstrating that these "orties" are animals; and with this important paper Peyssonel must necessarily have been familiar. Therefore, when he declared the "flowers" of the red coral to be little "orties," it was the same thing as saying that they were animals of the same general nature as sea-anemones. But to Peyssonel's contemporaries this was an extremely startling announcement. It was hard to imagine the existence of such a thing as an association of animals into a structure with stem and branches altogether like a plant, and fixed to the soil as a plant is fixed; and the naturalists of that day preferred not to imagine it. Even Reaumur could not bring himself to accept the notion, and France being blessed with Academicians, whose great function (as the late Bishop Wilson [116] and an eminent modern writer [117] have so well shown) is to cause sweetness and light to prevail, and to prevent such unmannerly fellows as Peyssonel from blurting out unedifying truths, they suppressed him; and, as aforesaid, his great work remained in manuscript, and may at this day be consulted by the curious in that state, in the Bibliotheque du Museum d'Histoire Naturelle. Peyssonel, who evidently was a person of savage and untameable disposition, so far from appreciating the kindness of the Academicians in giving him time to reflect upon the unreasonableness, not to say rudeness, of making public statements in opposition to the views of some of the most distinguished of their body, seems bitterly to have resented the treatment he met with. For he sent all further communications to the Royal Society of London, which never had, and it is to be hoped never will have, anything of an academic constitution; and finally he took himself off to Guadaloupe, and became lost to science altogether.
Fifteen or sixteen years after the date of Peyssonel's suppressed paper, the Abbe Trembley [118] published his wonderful researches upon the fresh-water Hydra. Bernard de Jussieu [119] and Guettard [120] followed them up by like inquiries upon the marine sea-anemones and corallines; Reaumur, convinced against his will of the entire justice of Peyssonel's views, adopted them, and made him a half-and-half apology in the preface to the next published volume of the "Memoires pour servir l'Histoire des Insectes;" and, from this time forth, Peyssonel's doctrine that corals are the work of animal organisms has been part of the body of established scientific truth.
Peyssonel, in the extract from his memoir already cited, compares the flower-like animal of the coral to a "poulpe," which is the French form of the name "polypus,"--"the many-footed,"--which the ancient naturalists gave to the soft-bodied cuttlefishes, which, like the coral animal, have eight arms, or tentacles, disposed around a central mouth. Reaumur, admitting the analogy indicated by Peyssonel, gave the name of polypes, not only to the sea-anemone, the coral animal, and the fresh-water Hydra, but to what are now known as the Polyzoa, and he termed the skeleton which they fabricate a "polypier," or "polypidom."
The progress of discovery, since Reaumur's time, has made us very completely acquainted with the structure and habits of all these polypes. We know that, among the sea-anemones and coral-forming animals, each poylpe has a mouth leading to a stomach, which is open at its inner end, and thus communicates freely with the general cavity of the body; that the tentacles placed round the mouth are hollow, and that they perform the part of arms in seizing and capturing prey. It is known that many of these creatures are capable of being multiplied by artificial division, the divided halves growing, after a time, into complete and separate animals; and that many are able to perform a very similar process naturally, in such a manner that one polype may, by repeated incomplete divisions, give rise to a sort of sheet, or turf, formed by innumerable connected, and yet independent, descendants. Or, what is still more common, a polype may throw out buds, which are converted into polypes, or branches bearing polypes, until a tree-like mass, sometimes of very considerable size, is formed.
This is what happens in the case of the red coral of commerce. A minute polype, fixed to the rocky bottom of the deep sea, grows up into a branched trunk. The end of every branch and twig is terminated by a polype; and all the polypes are connected together by a fleshy substance, traversed by innumerable canals which place each polype in communication with every other, and carry nourishment to the substance of the supporting stem. It is a sort of natural cooperative store, every polype helping the whole, at the same time as it helps itself. The interior of the stem, like that of the branches, is solidified by the deposition of carbonate of lime in its tissue, somewhat in the same fashion as our own bones are formed of animal matter impregnated with lime salts; and it is this dense skeleton (usually turned red by a peculiar colouring matter) cleared of the soft animal investment, as the hard wood of a tree might be stripped of its bark, which is the red coral.
In the case of the red coral, the hard skeleton belongs to the interior of the stem and branches only; but in the commoner white corals, each polype has a complete skeleton of its own. These polypes are sometimes solitary, in which case the whole skeleton is represented by a single cup, with partitions radiating from its centre to its circumference. When the polypes formed by budding or division remain associated, the polypidom is sometimes made up of nothing but an aggregation of these cups, while at other times the cups are at once separated and held together, by an intermediate substance, which represents the branches of the red coral. The red coral polype again is a comparatively rare animal, inhabiting a limited area, the skeleton of which has but a very insignificant mass; while the white corals are very common, occur in almost all seas, and form skeletons which are sometimes extremely massive.
With a very few exceptions, both the red and the white coral polypes are, in their adult state, firmly adherent to the sea-bottom; nor do their buds naturally become detached and locomotive. But, in addition to budding and division, these creatures possess the more ordinary methods of multiplication; and, at particular seasons, they give rise to numerous eggs of minute size. Within these eggs the young are formed, and they leave the egg in a condition which has no sort of resemblance to the perfect animal. It is, in fact, a minute oval body, many hundred times smaller than the full grown creature, and it swims about with great activity by the help of multitudes of little hair-like filaments, called cilia, with which its body is covered. These cilia all lash the water in one direction, and so drive the little body along as if it were propelled by thousands of extremely minute paddles. After enjoying its freedom for a longer or shorter time, and being carried either by the force of its own cilia, or by currents which bear it along, the embryo coral settles down to the bottom, loses its cilia, and becomes fixed to the rock, gradually assuming the polype form and growing up to the size of its parent. As the infant polypes of the coral may retain this free and active condition for many hours, or even days, and as a tidal or other current in the sea may easily flow at the speed of two or even more miles in an hour, it is clear that the embryo must often be transported to very considerable distances from the parent. And it is easily understood how a single polype, which may give rise to hundreds, or perhaps thousands, of embryos, may, by this process of partly active and partly passive migration, cover an immense surface with its offspring.
The masses of coral which may be formed by the assemblages of polypes which spring by budding, or by dividing, from a single polype, occasionally attain very considerable dimensions. Such skeletons are sometimes great plates, many feet long and several feet in thickness; or they may form huge half globes, like the brainstone corals, or may reach the magnitude of stout shrubs or even small trees. There is reason to believe that such masses as these take a long time to form, and hence that the age a polype tree, or polype turf, may attain, may be considerable. But, sooner or later, the coral polypes, like all other things, die; the soft flesh decays, while the skeleton is left as a stony mass at the bottom of the sea, where it retains its integrity for a longer or a shorter time, according as its position affords more or less protection from the wear and tear of the waves.
The polypes which give rise to the white coral are found, as has been said, in the seas of all parts of the world; but in the temperate and cold oceans they are scattered and comparatively small in size, so that the skeletons of those which die do not accumulate in any considerable quantity. But it is otherwise in the greater part of the ocean which lies in the warmer parts of the world, comprised within a distance of about eighteen hundred miles on each side of the equator. Within the zone thus bounded, by far the greater part of the ocean is inhabited by coral polypes, which not only form very strong and large skeletons, but associate together into great masses, like the thickets and the meadow turf, or, better still, the accumulations of peat, to which plants give rise on dry land. These masses of stony matter, heaped up beneath the waters of the ocean, become as dangerous to mariners as so much ordinary rock, and to these, as to the common rock ridges, the seaman gives the name of "reefs."
Such coral reefs cover many thousand square miles in the Pacific and in the Indian Oceans. There is one reef, or rather great series of reefs, called the Barrier Reef, which stretches, almost continuously, for more than eleven hundred miles off the east coast of Australia. Multitudes of the islands in the Pacific are either reefs themselves, or are surrounded by reefs. The Red Sea is in many parts almost a maze of such reefs, and they abound no less in the West Indies, along the coast of Florida, and even as far north as the Bahama Islands. But it is a very remarkable circumstance that, within the area of what we may call the "coral zone," there are no coral reefs upon the west coast of America, nor upon the west coast of Africa; and it is a general fact that the reefs are interrupted, or absent, opposite the mouths of great rivers. The causes of this apparent caprice in the distribution of coral reefs are not far to seek. The polypes which fabricate them require for their vigorous growth a temperature which must not fall below 68 degrees Fahrenheit all the year round, and this temperature is only to be found within the distance on each side of the equator which has been mentioned, or thereabouts. But even within the coral zone this degree of warmth is not everywhere to be had. On the west coast of America, and on the corresponding coast of Africa, the currents of cold water from the icy regions which surround the South Pole set northward, and it appears to be due to their cooling influence that the sea in these regions is free from the reef builders. Again, the coral polypes cannot live in water which is rendered brackish by floods from the land, or which is perturbed by mud from the same source, and hence it is that they cease to exist opposite the mouths of rivers, which damage them in both these ways.
Such is the general distribution of the reef-building corals, but there are some very interesting and singular circumstances to be observed in the conformation of the reefs, when we consider them individually. The reefs, in fact, are of three different kinds; some of them stretch out from the shore, almost like a prolongation of the beach, covered only by shallow water, and in the case of an island, surrounding it like a fringe of no considerable breadth. These are termed "fringing reefs." Others are separated by a channel which may attain a width of many miles, and a depth of twenty or thirty fathoms or more, from the nearest land; and when this land is an island, the reef surrounds it like a low wall, and the sea between the reef and the land is, as it were, a moat inside this wall. Such reefs as these are called "encircling" when they surround an island; and "barrier" reefs, when they stretch parallel with the coast of a continent. In both these cases there is ordinary dry land inside the reef, and separated from it only by a narrower or a wider, a shallower or a deeper, space of sea, which is called a "lagoon," or "inner passage." But there is a third kind of reef, of very common occurrence in the Pacific and Indian Oceans, which goes by the name of "atoll." This is, to all intents and purposes, an encircling reef, without anything to encircle; or, in other words, without an island in the middle of its lagoon. The atoll has exactly the appearance of a vast, irregularly oval, or circular, breakwater, enclosing smooth water in its midst. The depth of the water in the lagoon rarely exceeds twenty or thirty fathoms, but, outside the reef, it deepens with great rapidity to two hundred or three hundred fathoms. The depth immediately outside the barrier, or encircling, reefs, may also be very considerable; but, at the outer edge of a fringing reef, it does not amount usually to more than twenty or twenty-five fathoms; in other words, from one hundred and twenty to one hundred and fifty feet.
Thus, if the water of the ocean should be suddenly drained away, we should see the atolls rising from the sea-bed like vast truncated cones, and resembling so many volcanic craters, except that their sides would be steeper than those of an ordinary volcano. In the case of the encircling reefs, the cone, with the enclosed island, would look like Vesuvius with Monte Nuovo within the old crater of Somma;[121] while, finally, the island with a fringing reef would have the appearance of an ordinary hill, or mountain, girded by a vast parapet, within which would lie a shallow moat. And the dry bed of the Pacific might afford grounds for an inhabitant of the moon to speculate upon the extraordinary subterranean activity to which these vast and numerous "craters" bore witness!
When the structure of a fringing reef is investigated, the bottom of the lagoon is found to be covered with fine whitish mud, which results from the breaking up of the dead corals. Upon this muddy floor there lie, here and there, growing corals, or occasionally great blocks of dead coral, which have been torn by storms from the outer edge of the reef, and washed into the lagoon. Shellfish and worms of various kinds abound; and fish, some of which prey upon the coral, sport in the deeper pools. But the corals which are to be seen growing in the shallow waters of the lagoon are of a different kind from those which abound on the outer edge of the reef, and of which the reef is built up. Close to the seaward edge of the reef, over which, even in calm weather, a surf almost always breaks, the coral rock is encrusted with a thick coat of a singular vegetable organism, which contains a great deal of lime--the so-called Nullipora. Beyond this, in the part of the edge of the reef which is always covered by the breaking waves, the living, true, reef-polypes make their appearance; and, in different forms, coat the steep seaward face of the reef to a depth of one hundred or even one hundred and fifty feet. Beyond this depth the sounding-lead rests, not upon the wall-like face of the reef, but on the ordinary shelving sea-bottom. And the distance to which a fringing reef extends from the land corresponds with that at which the sea has a depth of twenty or five-and-twenty fathoms.
If, as we have supposed, the sea could be suddenly withdrawn from around an island provided with a fringing reef, such as the Mauritius,[122] the reef would present the aspect of a terrace, its seaward face, one hundred feet or more high, blooming with the animal flowers of the coral, while its surface would be hollowed out into a shallow and irregular moat-like excavation.