Among the bones, however, respecting the authenticity of which there seems no doubt, may be mentioned those of the elephant, horse, pig, deer, and the jaws and teeth of field mice (fig. 141.). I have seen the tusk of an elephant from Bramerton near Norwich, to which, many serpulæ were attached, showing that it had lain for some time at the bottom of the sea of the Norwich Crag.

At Thorpe, near Aldborough, and at Southwold, in Suffolk, this fluvio-marine formation is well exposed in the sea-cliffs, consisting of sand, shingle, loam, and laminated clay. Some of the strata there bear the marks of tranquil deposition, and in one section a thickness of 40 feet is sometimes exposed to view. Some of the lamellibranchiate shells have both valves united, although mixed with land and freshwater testacea, and with the bones and teeth of elephant, rhinoceros, horse, and deer. Captain Alexander, with whom I examined these strata in 1835, showed me a bed rich in marine shells, in which he had found a large specimen of the Fusus striatus, filled with sand, and in the interior of which was the tooth of a horse.

Among the freshwater shells I obtained the Cyrena consobrina (fig. 26. p. 28.), before mentioned, supposed to agree with a species now living in the Nile.

I formerly classed the Norwich Crag as older Pliocene, conceiving that more than a third of the fossil testacea were extinct; but there now seems good reason for believing that several of the rarer shells obtained from these strata do not really belong to a contemporary fauna, but have been washed out of the older beds of the "Red Crag;" while other species, once supposed to have died out, have lately been met with living in the British seas. According to Mr. Searles Wood, the total number of marine species does not exceed seventy-six, of which one tenth only are extinct. Of the fourteen associated freshwater shells, all the species appear to be living. Strata containing the same shells as those near Norwich have been found by Mr. Bean, at Bridlington, in Yorkshire.

Newer Pliocene strata of Sicily.—In no part of Europe are the Newer Pliocene formations seen to enter so largely into the structure of the earth's crust, or to rise to such heights above the level of the sea, as in Sicily. They cover nearly half the island, and near its centre, at Castrogiovanni, they reach an elevation of 3000 feet. They consist principally of two divisions, the upper calcareous, the lower argillaceous, both of which may be seen at Syracuse, Girgenti, and Castrogiovanni.

According to Philippi, to whom we are indebted for the best account of the tertiary shells of this island, thirty-five species out of one hundred and twenty-four obtained from the beds in central Sicily are extinct. Of the remainder, which still live, five species are no longer inhabitants of the Mediterranean. When I visited Sicily in 1828 I estimated the proportion of living species as somewhat greater, partly because I confounded with the tertiary formation of central Sicily the strata at the base of Etna, and some other localities, where the fossils are now proved to agree entirely with the present Mediterranean fauna.

Philippi came to the conclusion, that in Sicily there is a gradual passage from beds containing 70 per cent. of recent shells, to those in which the whole of the fossils are identical with recent species; but his tables appear scarcely to bear out so important a generalization, several of the places cited by him in confirmation having as yet furnished no more than twenty or thirty species of testacea. The Sicilian beds in question probably belong to about the same period as the Norwich Crag, although a geologist, accustomed to see nearly all the Pleistocene formations in the north of Europe occupying low grounds and very incoherent in texture, is naturally surprised to behold formations of the same age so solid and stony, of such thickness, and attaining so great an elevation above the level of the sea.

The upper or calcareous member of this group in Sicily consists in some places of a yellowish-white stone, like the calcaire grossier of Paris, in others, of a rock nearly as compact as marble. Its aggregate thickness amounts sometimes to 700 or 800 feet. It usually occurs in regular horizontal beds, and is occasionally intersected by deep valleys, such as those of Sortino and Pentalica, in which are numerous caverns. The fossils are in every stage of preservation, from shells retaining portions of their animal matter and colour, to others which are mere casts.

The limestone passes downwards into a sandstone and conglomerate, below which is clay and blue marl, like that of the Subapennine hills, from which perfect shells and corals may be disengaged. The clay sometimes alternates with yellow sand.

South of the plain of Catania is a region in which the tertiary beds are intermixed with volcanic matter, which has been for the most part the product of submarine eruptions. It appears that, while the clay, sand, and yellow limestone before mentioned were in course of deposition at the bottom of the sea, volcanos burst out beneath the waters, like that of Graham Island, in 1831, and these explosions recurred again and again at distant intervals of time. Volcanic ashes and sand were showered down and spread by the waves and currents so as to form strata of tuff, which are found intercalated between beds of limestone and clay containing marine shells, the thickness of the whole mass exceeding 2000 feet. The fissures through which the lava rose may be seen in many places forming what are called dikes.

In part of the region above alluded to, as, for example, near Lentini, a conglomerate occurs in which I observed many pebbles of volcanic rocks covered by full grown serpulæ. We may explain the origin of these by supposing that there were some small volcanic islands which may have been destroyed from time to time by the waves, as Graham Island has been swept away since 1831. The rounded blocks and pebbles of solid volcanic matter, after being rolled for a time on the beach of such temporary islands, were carried at length into some tranquil part of the sea, where they lay for years, while the marine serpulæ adhered to them, their shells growing and covering their surface, as they are seen adhering to the shell figured in p. 22. Finally, the bed of pebbles was itself covered with strata of shelly limestone. At Vizzini, a town not many miles distant to the S.W., I remarked another striking proof of the gradual manner in which these modern rocks were formed, and the long intervals of time which elapsed between the pouring out of distinct sheets of lava. A bed of oysters no less than 20 feet in thickness rests upon a current of basaltic lava. The oysters are perfectly identifiable with our common eatable species. Upon the oyster bed, again, is superimposed a second mass of lava, together with tuff or peperino. In the midst of the same alternating igneous and aqueous formations is seen near Galieri, not far from Vizzini, a horizontal bed, about a foot and a half in thickness, composed entirely of a common Mediterranean coral (Caryophyllia cæspitosa, Lam.). These corals stand erect as they grew; and, after being traced for hundreds of yards, are again found at a corresponding height on the opposite side of the valley.

The corals are usually branched, but not by the division of the animals as some have supposed, but by the attachment of young individuals to the sides of the older ones; and we must understand this mode of increase, in order to appreciate the time which was required for the building up of the whole bed of coral during the growth of many successive generations.[152-A]

Among the other fossil shells met with in these Sicilian strata, which still continue to abound in the Mediterranean, no shell is more conspicuous, from its size and frequent occurrence, than the great scallop, Pecten jacobæus (see fig. 124.), now so common in the neighbouring seas. We see this shell in the calcareous beds at Palermo in great numbers, in the limestone at Girgenti, and in that which alternates with volcanic rocks in the country between Syracuse and Vizzini, often at great heights above the sea.

The more we reflect on the preponderating number of these recent shells, the more we are surprised at the great thickness, solidity, and height above the sea of the rocky masses in which they are entombed, and the vast amount of geographical change which has taken place since their origin. It must be remembered that, before they began to emerge, the uppermost strata of the whole must have been deposited under water. In order, therefore, to form a just conception of their antiquity, we must first examine singly the innumerable minute parts of which the whole is made up, the successive beds of shells, corals, volcanic ashes, conglomerates, and sheets of lava; and we must afterwards contemplate the time required for the gradual upheaval of the rocks, and the excavation of the valleys. The historical period seems scarcely to form an appreciable unit in this computation, for we find ancient Greek temples, like those of Girgenti (Agrigentum), built of the modern limestone of which we are speaking, and resting on a hill composed of the same; the site having remained to all appearance unaltered since the Greeks first colonised the island.

The modern geological date of the rocks in this region leads to another singular and unexpected conclusion, namely, that the fauna and flora of a large part of Sicily are of higher antiquity than the country itself, having not only flourished before the lands were raised from the deep, but even before their materials were brought together beneath the waters. The chain of reasoning which conducts us to this opinion may be stated in a few words. The larger part of the island has been converted from sea into land since the Mediterranean was peopled with nearly all the living species of testacea and zoophytes. We may therefore presume that, before this region emerged, the same land and river shells, and almost all the same animals and plants, were in existence which now people Sicily; for the terrestrial fauna and flora of this island are precisely the same as that of other lands surrounding the Mediterranean. There appear to be no peculiar or indigenous species, and those which are now established there must be supposed to have migrated from pre-existing lands, just as the plants and animals of the Neapolitan territory have colonised Monte Nuovo, since that volcanic cone was thrown up in the sixteenth century.

Such conclusions throw a new light on the adaptation of the attributes and migratory habits of animals and plants to the changes which are unceasingly in progress in the physical geography of the globe. It is clear that the duration of species is so great, that they are destined to outlive many important revolutions in the configuration of the earth's surface; and hence those innumerable contrivances for enabling the subjects of the animal and vegetable creation to extend their range; the inhabitants of the land being often carried across the ocean, and the aquatic tribes over great continental spaces. It is obviously expedient that the terrestrial and fluviatile species should not only be fitted for the rivers, valleys, plains, and mountains which exist at the era of their creation, but for others that are destined to be formed before the species shall become extinct; and, in like manner, the marine species are not only made for the deep and shallow regions of the ocean existing at the time when they are called into being, but for tracts that may be submerged or variously altered in depth during the time that is allotted for their continuance on the globe.

OSSEOUS BRECCIAS AND DEPOSITS IN CAVES OF THE PLIOCENE PERIOD.

Sicily.—Caverns filled with marine breccias, at the base of ancient sea-cliffs, have been already mentioned in the sixth chapter; and it was noticed, respecting the cave of San Ciro, near Palermo (p. 75.), that upon a bed of sand filled with sea-shells, almost all of recent species, rests a breccia (b, fig. 93.), composed of fragments of calcareous rock, and the bones of animals. In the sand at the bottom of that cave, Dr. Philippi found about forty-five marine shells, all clearly identical with recent species, except two or three. The bones in the incumbent breccia are chiefly those of the mammoth (E. primigenius), with some belonging to an hippopotamus, distinct from the recent species, and smaller than that usually found fossil. (See fig. 132.) Several species of deer also, and, according to some accounts, the remains of a bear, were discovered. These mammalia are probably referable to the Post-Pliocene period.

The Newer Pliocene tertiary limestone of the south of Sicily, already described, is sometimes full of caverns; and the student will at once perceive that all the quadrupeds of which the remains are found in the stalactite of these caverns, being of later origin than the rocks, must be referable to the close of the tertiary epoch, if not of still later date. The situation of one of these caves, in the valley of Sortino, is represented in the annexed section.

No less than thirty-seven species of mammalia are enumerated by Professor Owen as having been discovered in the caves of the British islands, of which eighteen appear to be extinct, while the others still survive in Europe. They were not washed to the spots where the fossils now occur by a great flood; but lived and died, one generation after another, in the places where they lie buried. Among other arguments in favour of this conclusion may be mentioned the great numbers of the shed antlers of deer discovered in caves and in freshwater strata throughout England.[155-A]

Examples also occur of fissures into which animals have fallen from time to time, or have been washed in from above, together with alluvial matter and fragments of rock detached by frost, forming a mass which may be united into a bony breccia by stalagmitic infiltrations. Frequently we discover a long suite of caverns connected by narrow and irregular galleries, which hold a tortuous course through the interior of mountains, and seem to have served as the subterranean channels of springs and engulphed rivers. Many streams in the Morea are now carrying bones, pebbles, and mud into underground passages of this kind.[155-B] If, at some future period, the form of that country should be wholly altered by subterranean movements and new valleys shaped out by denudation, many portions of the former channels of these engulphed streams may communicate with the surface, and become the dens of wild beasts, or the recesses to which quadrupeds retreat to die. Certain caves of France, Germany, and Belgium, may have passed successively through these different conditions, and in their last state may have remained open to the day for several tertiary periods. It is nevertheless remarkable, that on the continent of Europe, as in England, the fossil remains of mammalia belong almost exclusively to those of the Newer Pliocene and Post-Pliocene periods, and not to the Miocene or Eocene epochs, and when they are accompanied by land or river shells, these agree in great part, or entirely, with recent species.

As the preservation of the fossil bones is due to a slow and constant supply of stalactite, brought into the caverns by water dropping from the roof, the source and origin of this deposit has been a subject of curious inquiry. The following explanation of the phenomenon has been recently suggested by the eminent chemist Liebig. On the surface of Franconia, where the limestone abounds in caverns, is a fertile soil, in which vegetable matter is continually decaying. This mould or humus, being acted on by moisture and air, evolves carbonic acid which is dissolved by rain. The rain water, thus impregnated, permeates the porous limestone, dissolves a portion of it, and afterwards, when the excess of carbonic acid evaporates in the caverns, parts with the calcareous matter, and forms stalactite.

Australian cave-breccias.—Ossiferous breccias are not confined to Europe, but occur in all parts of the globe; and those lately discovered in fissures and caverns in Australia correspond closely in character with what has been called the bony breccia of the Mediterranean, in which the fragments of bone and rock are firmly bound together by a red ochreous cement.

Some of these caves have been examined by Sir T. Mitchell in the Wellington Valley, about 210 miles west of Sidney, on the river Bell, one of the principal sources of the Macquarie, and on the Macquarie itself. The caverns often branch off in different directions through the rock, widening and contracting their dimensions, and the roofs and floors are covered with stalactite. The bones are often broken, but do not seem to be water-worn. In some places they lie imbedded in loose earth, but they are usually included in a breccia.

The remains found most abundantly are those of the kangaroo, of which there are four species, besides which the genera Hypsiprymnus, Phalangista, Phascolomys, and Dasyurus, occur. There are also bones, formerly conjectured by some osteologists to belong to the hippopotamus, and by others to the dugong, but which are now referred by Mr. Owen to a marsupial genus, allied to the Wombat.

In the fossils above enumerated, several species are larger than the largest living ones of the same genera now known in Australia. The annexed figure of the right side of a lower jaw of a kangaroo (Macropus atlas, Owen) will at once be seen to exceed in magnitude the corresponding part of the largest living kangaroo, which is represented in fig. 127. In both these specimens part of the substance of the jaw has been broken open, so as to show the permanent false molar (a. fig. 126.) concealed in the socket. From the fact of this molar not having been cut, we learn that the individual was young, and had not shed its first teeth. In fig. 128. a front tooth of the same species of kangaroo is represented.

There are indeed some cosmopolite genera, such as the Mastodon (a genus of the elephant family), and the horse, which were simultaneously represented by different fossil species in Europe, North America, and South America; but these few exceptions can by no means invalidate the rule which has been thus expressed by Professor Owen, "that in the highest organized class of animals the same forms were restricted to the same great provinces at the Pliocene periods as they are at the present day."

However modern, in a geological point of view, we may consider the Pleistocene epoch, it is evident that causes more general and powerful than the intervention of man have occasioned the disappearance of the ancient fauna from so many extensive regions. Not a few of the species had a wide range; the same Megatherium, for instance, extended from Patagonia and the river Plata in South America, between latitudes 31° and 39° south, to corresponding latitudes in North America, the same animal being also an inhabitant of the intermediate country of Brazil, where its fossil remains have been met with in caves. The extinct elephant, likewise, of Georgia (Elephas primigenius) has been traced in a fossil state northward from the river Alatamaha, in lat. 33° 50' N. to the polar regions, and then again in the eastern hemisphere from Siberia to the south of Europe. If it be objected that, notwithstanding the adaptation of such quadrupeds to a variety of climates and geographical conditions, their great size exposed them to extermination by the first hunter tribes, we may observe that the investigations of Lund and Clausen in the ossiferous limestone caves of Brazil have demonstrated that these large mammalia were associated with a great many smaller quadrupeds, some of them as diminutive as field mice, which have all died out together, while the land shells formerly their contemporaries still continue to exist in the same countries. As we may feel assured that these minute quadrupeds could never have been extirpated by man, so we may conclude that all the species, small and great, have been annihilated one after the other, in the course of indefinite ages, by those changes of circumstances in the organic and inorganic world which are always in progress, and are capable in the course of time of greatly modifying the physical geography, climate, and all other conditions on which the continuance upon the earth of any living being must depend.[158-A]

The law of geographical relationship above alluded to, between the living vertebrata of every great zoological province and the fossils of the period immediately antecedent, even where the fossil species are extinct, is by no means confined to the mammalia. New Zealand, when first examined by Europeans, was found to contain no indigenous land quadrupeds, no kangaroos, or opossums, like Australia; but a wingless bird abounded there, the smallest living representative of the ostrich family, called the Xivi, by the natives (Apteryx). In the fossils of the Post-Pliocene and Pleistocene period in this same island, there is the like absence of kangaroos, opossums, wombats, and the rest; but in their place a prodigious number of well preserved specimens of gigantic birds of the struthious order, called by Owen Dinornis and Palapteryx, which are entombed in superficial deposits. These genera comprehended many species, some of which were 4, some 7, others 9, and others 11 feet in height! It seems doubtful whether any contemporary mammalia shared the land with this population of gigantic feathered bipeds.

To those who have never studied comparative anatomy it may seem scarcely credible, that a single bone taken from any part of the skeleton may enable a skilful osteologist to distinguish, in many cases, the genus, and sometimes the species, of quadruped to which it belonged. Although few geologists can aspire to such knowledge, which must be the result of long practice and study, they will nevertheless derive great advantage from learning what is comparatively an easy task, to distinguish the principal divisions of the mammalia by the forms and characters of their teeth. The annexed figures, all taken from original specimens, may be useful in assisting the student to recognize the teeth of many genera most frequently found fossil in Europe:—

CHAPTER XIV.

OLDER PLIOCENE AND MIOCENE FORMATIONS.

The older Pliocene strata, which next claim our attention, are chiefly confined, in Great Britain, to the eastern part of the county of Suffolk, where, like the Norwich beds already described, they are called "Crag," a provincial name given particularly to those masses of shelly sand which have been used from very ancient times in agriculture, to fertilize soils deficient in calcareous matter. The relative position of the "red crag" in Essex to the London clay, may be understood by reference to the accompanying diagram (fig. 142.).

The Suffolk crag is divisible into two masses, the upper of which has been termed the Red, and the lower the Coralline Crag.[162-A] The upper deposit consists chiefly of quartzose sand, with an occasional intermixture of shells, for the most part rolled, and sometimes comminuted. The lower or Coralline crag is of very limited extent, ranging over an area about 20 miles in length, and 3 or 4 in breadth, between the rivers Alde and Stour. It is generally calcareous and marly—a mass of shells and small corals, passing occasionally into a soft building stone. At Sudbourn, near Orford, where it assumes this character, are large quarries, in which the bottom of it has not been reached at the depth of 50 feet. At some places in the neighbourhood, the softer mass is divided by thin flags of hard limestone, and corals placed in the upright position in which they grew.

The Red crag is distinguished by the deep ferruginous or ochreous colour of its sands and fossils, the Coralline by its white colour. Both formations are of moderate thickness; the red crag rarely exceeding 40, and the coralline seldom amounting to 20, feet. But their importance is not to be estimated by the density of the mass of strata or its geographical extent, but by the extraordinary richness of its organic remains, belonging to a very peculiar type, which seems to characterize the state of the living creation in the north of Europe during the older Pliocene era.

For a large collection of the fish, echinoderms, shells, and corals of the deposits in Suffolk, we are indebted to the labours of Mr. Searles Wood. Of testacea alone he has obtained from 230 species from the Red, and 345 from the Coralline crag, about 150 being common to each. The proportion of recent species in the new group is considered by Mr. Wood to be about 70[162-B] per cent., and that in the older or coralline about 60. When I examined these shells of Suffolk in 1835, with the assistance of Dr. Beck, Mr. George Sowerby, Mr. Searles Wood, and other eminent conchologists, I came to the opinion that the extinct species predominated very decidedly in number over the living. Recent investigations, however, have thrown much new light on the conchology of the Arctic, Scandinavian, British, and Mediterranean Seas. Many of the species formerly known only as fossils of the Crag, and supposed to have died out, have been dredged up in a living state from depths not previously explored. Other recent species, before regarded as distinct from the nearest allied Crag fossils, have been observed, when numerous individuals were procured, to be liable to much greater variation, both in size and form, than had been suspected, and thus have been identified. Consequently, the Crag fauna has been found to approach much more nearly to the recent fauna of the Northern, British, and Mediterranean Seas than had been imagined. The analogy of the whole group of testacea to the European type is very marked, whether we refer to the large development of certain genera in number of species or to their size, or to the suppression or feeble representation of others. The indication also afforded by the entire fauna of a climate not much warmer than that now prevailing in corresponding latitudes, prepares us to believe that they are not of higher antiquity than the Older Pliocene era.[163-A]

The position of the red crag in Essex to the subjacent London clay and chalk has been already pointed out (fig. 142.). Whenever the two divisions are met with in the same district, the red crag lies uppermost; and, in some cases, as in the section represented in fig. 143., it is observed that the older or coralline mass b had suffered denudation before the newer formation a was thrown down upon it. At D there is not only a distinct cliff, 8 or 10 feet high, of coralline crag, running in a direction N.E. and S.W., against which the red crag abuts with its horizontal layers; but this cliff occasionally overhangs. The rock composing it is drilled everywhere by Pholades, the holes which they perforated having been afterwards filled with sand and covered over when the newer beds were thrown down. As the older formation is shown by its fossils to have accumulated in a deeper sea (15, and sometimes 25, fathoms deep or more), there must no doubt have been an upheaval of the sea-bottom before the cliff here alluded to was shaped out. We may also conclude that so great an amount of denudation could scarcely take place, in such incoherent materials, without many of the fossils of the inferior beds becoming mixed up with the overlying crag, so that considerable difficulty must be occasionally experienced by the palæontologist in deciding which species belong severally to each group. The red crag being formed in a shallower sea, often resembles in structure a shifting sand bank, its layers being inclined diagonally, and the planes of stratification being sometimes directed in the same quarry to the four cardinal points of the compass, as at Butley. That in this and many other localities, such a structure is not deceptive or due to any subsequent concretionary re-arrangement of particles, or to mere lines of colour, is proved by each bed being made up of flat pieces of shell which lie parallel to the planes of the smaller strata.

Some fossils, which are very abundant in the red crag, have never been found in the white or coralline division; as, for example, the Fusus contrarius (fig. 144.), and several species of Buccinum (or Nassa) and Murex (see figs. 145, 146.), which two genera seem wanting in the lower crag.