The Elements of Geology, William Harmon Norton [e textbook reader TXT] 📗
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The tapirs are an ancient family which has changed but little since it separated from the other perissodactyl stocks in the early Tertiary. At present, tapirs are found only in South America and southern Asia,—a remarkable distribution which we could not explain were it not that the geological record shows that during Tertiary times tapirs ranged throughout the northern hemisphere, making their way to South America late in that period. During the Pleistocene they became extinct over all the intervening lands between the widely separated regions where now they live. The geographic distribution of animals, as well as their relationships and origins, can be understood only through a study of their geological history.
THE PROBOSCIDIANS. This unique order of hoofed mammals, of which the elephant is the sole survivor, began, so far as known, in the Eocene, in Egypt, with a piglike ancestor the size of a small horse, with cheek teeth like the Mastodon's, but wanting both trunk and tusks. A proboscidian came next with four short tusks, and in the Miocene there followed a Mastodon (Fig. 346) armed with two pairs of long, straight tusks on which rested a flexible proboscis.
The DINOTHERE was a curious offshoot of the line, which developed in the Miocene in Europe. In this immense proboscidian, whose skull was three feet long, the upper pair of tusks had disappeared, and those of the lower jaw were bent down with a backward curve in walrus fashion.
In the true ELEPHANTS, which do not appear until near the close of the Tertiary, the lower jaw loses its tusks and the grinding teeth become exceedingly complex in structure. The grinding teeth of the mastodon had long roots and low crowns crossed by four or five peaked enameled ridges. In the teeth of the true elephants the crown has become deep, and the ridges of enamel have changed to numerous upright, platelike folds, their interspaces filled with cement. The two genera—Mastodon and Elephant—are connected by species whose teeth are intermediate in pattern. The proboscidians culminated in the Pliocene, when some of the giant elephants reached a height of fourteen feet.
THE ARTIODACTYLS comprise the hoofed Mammalia which have an even number of toes, such as cattle, sheep, and swine. Like the perissodactyls, they are descended from the primitive five-toed plantigrade mammals of the lowest Eocene. In their evolution, digit number one was first dropped, and the middle pair became larger and more massive, while the side digits, numbers two and five, became shorter, weaker, and less serviceable. The FOUR-TOED ARTIODACTYLS culminated in the Tertiary; at present they are represented only by the hippopotamus and the hog. Along the main line of the evolution of the artiodactyls the side toes, digits two and five, disappeared, leaving as proof that they once existed the corresponding bones of palm and sole as splints. The TWO-TOED ARTIODACTYLS, such as the camels, deer, cattle, and sheep, are now the leading types of the herbivores.
SWINE AND PECCARIES are two branches of a common stock, the first developing in the Old World and the second in the New. In the Miocene a noticeable offshoot of the line was a gigantic piglike brute, a root eater, with a skull a yard in length, whose remains are now found in Colorado and South Dakota.
CAMELS AND LLAMAS. The line of camels and llamas developed in North America, where the successive changes from an early Eocene ancestor, no larger than a rabbit, are traced step by step to the present forms, as clearly as is the evolution of the horse. In the late Miocene some of the ancestral forms migrated to the Old World by way of a land connection where Bering Strait now is, and there gave rise to the camels and dromedaries. Others migrated into South America, which had now been connected with our own continent, and these developed into the llamas and guanacos, while those of the race which remained in North America became extinct during the Pleistocene.
Some peculiar branches of the camel stem appeared in North America. In the Pliocene arose a llama with the long neck and limbs of a giraffe, whose food was cropped from the leaves and branches of trees. Far more generalized in structure was the Oreodon, an animal related to the camels, but with distinct affinities also with other lines, such as those of the hog and deer. These curious creatures were much like the peccary in appearance, except for their long tails. In the middle Eocene they roamed in vast herds from Oregon to Kansas and Nebraska.
THE RUMINANTS. This division of the artiodactyls includes antelopes, deer, oxen, bison, sheep, and goats,—all of which belong to a common stock which took its rise in Europe in the upper Eocene from ancestral forms akin to those of the camels. In the Miocene the evolution of the two-toed artiodactyl foot was well-nigh completed. Bonelike growths appeared on the head, and the two groups of the ruminants became specialized,—the deer with bony antlers, shed and renewed each year, and the ruminants with hollow horns, whose two bony knobs upon the skull are covered with permanent, pointed, horny sheaths.
The ruminants evolved in the Old World, and it was not until the later Miocene that the ancestors of the antelope and of some deer found their way to North America. Mountain sheep and goats, the bison and most of the deer, did not arrive until after the close of the Tertiary, and sheep and oxen were introduced by man.
The hoofed mammals of the Tertiary included many offshoots from the main lines which we have traced. Among them were a number of genera of clumsy, ponderous brutes, some almost elephantine in their bulk.
THE CARNIVORES. The ancestral lines of the families of the flesh eaters—such as the cats (lions, tigers, etc.), the bears, the hyenas, and the dogs (including wolves and foxes)—converge in the creodonts of the early Eocene,—an order so generalized that it had affinities not only with the carnivores but also with the insect eaters, the marsupials, and the hoofed mammals as well. From these primitive flesh eaters, with small and simple brains, numerous small teeth, and plantigrade tread, the different families of the carnivores of the present have slowly evolved.
DOGS AND BEARS. The dog family diverged from the creodonts late in the Eocene, and divided into two branches, one of which evolved the wolves and the other the foxes. An offshoot gave rise to the family of the bears, and so closely do these two families, now wide apart, approach as we trace them back in Tertiary times that the Amphicyon, a genus doglike in its teeth and bearlike in other structures, is referred by some to the dog and by others to the bear family. The well-known plantigrade tread of bears is a primitive characteristic which has survived from their creodont ancestry.
CATS. The family of the cats, the most highly specialized of all the carnivores, divided in the Tertiary into two main branches. One, the saber-tooth tigers (Fig. 351), which takes its name from their long, saberlike, sharp-edged upper canine teeth, evolved a succession of genera and species, among them some of the most destructive beasts of prey which ever scourged the earth. They were masters of the entire northern hemisphere during the middle Tertiary, but in Europe during the Pliocene they declined, from unknown causes, and gave place to the other branch of cats,—which includes the lions, tigers, and leopards. In the Americas the saber-tooth tigers long survived the epoch.
MARINE MAMMALS. The carnivorous mammals of the sea—whales, seals, walruses, etc.—seem to have been derived from some of the creodonts of the early Tertiary by adaptation to aquatic life. Whales evolved from some land ancestry at a very early date in the Tertiary; in the marine deposits of the Eocene are found the bones of the Zeuglodon, a whalelike creature seventy feet in length.
PRIMATES. This order, which includes lemurs, monkeys, apes, and man, seems to have sprung from a creodont or insectivorous ancestry in the lower Eocene. Lemur-like types, with small, smooth brains, were abundant in the United States in the early Tertiary, but no primates have been found here in the middle Tertiary and later strata. In Europe true monkeys were introduced in the Miocene, and were abundant until the close of the Tertiary, when they were driven from the continent by the increasing cold.
ADVANCE OF THE MAMMALIA DURING THE TERTIARY. During the several millions of years comprised in Tertiary time the mammals evolved from the lowly, simple types which tenanted the earth at the beginning of the period, into the many kinds of highly specialized mammals of the Pleistocene and the present, each with the various structures of the body adapted to its own peculiar mode of life. The swift feet of the horse, the horns of cattle and the antlers of the deer, the lion's claws and teeth, the long incisors of the beaver, the proboscis of the elephant, were all developed in Tertiary times. In especial the brain of the Tertiary mammals constantly grew larger relatively to the size of body, and the higher portion of the brain—the cerebral lobes—increased in size in comparison with the cerebellum. Some of the hoofed mammals now have a brain eight or ten times the size of that of their early Tertiary predecessors of equal bulk. Nor can we doubt that along with the increasing size of brain went a corresponding increase in the keenness of the senses, in activity and vigor, and in intelligence.
CHAPTER XXII THE QUATERNARYThe last period of geological history, the Quaternary, may be said to have begun when all, or nearly all, living species of mollusks and most of the existing mammals had appeared.
It is divided into two great epochs. The first, the Pleistocene or Glacial epoch, is marked off from the Tertiary by the occupation of the northern parts of North America and Europe by vast ice sheets; the second, the Recent epoch, began with the disappearance of the ice sheets from these continents, and merges into the present time.
THE PLEISTOCENE EPOCHWe now come to an episode of unusual interest, so different was it from most of the preceding epochs and from the present, and so largely has it influenced the conditions of man's life.
The records of the Glacial epoch are so plain and full that we are compelled to believe what otherwise would seem almost incredible, —that following the mild climate of the Tertiary came a succession of ages when ice fields, like that of Greenland, shrouded the northern parts of North America and Europe and extended far into temperate latitudes.
THE DRIFT. Our studies of glaciers have prepared us to decipher and interpret the history of the Glacial epoch, as it is recorded in the surface deposits known as the drift. Over most of Canada and the northern states this familiar formation is exposed to view in nearly all cuttings which pass below the surface soil. The drift includes two distinct classes of deposits,—the unstratified drift laid down by glacier ice, and the stratified drift spread by glacier waters.
The materials of the drift are in any given place in part unlike the rock on which it rests. They cannot be derived from the underlying rock by weathering, but have been brought from elsewhere. Thus where a region is underlain by sedimentary rocks, as is the drift-covered area from the Hudson River to the Missouri, the drift contains not only fragments of limestone, sandstone, and shale of local derivation, but also pebbles of many igneous and metamorphic rocks, such as granites, gneisses, schists, dike rocks, quartzites, and the quartz of mineral veins, whose nearest source is the Archean area of Canada and the states of our northern border. The drift received its name when it was supposed that the formation had been drifted by floods and icebergs from outside sources,—a theory long since abandoned.
The distribution also of the drift points clearly to its peculiar origin. Within the limits of the glaciated area it covers the country without regard to the relief, mantling with its debris not only lowlands and valleys but also highlands and mountain slopes.
The boundary of the drift is equally independent of the relief of the land, crossing hills and plains impartially, unlike water-laid deposits, whose margins, unless subsequently deformed, are horizontal. The boundary of the drift is strikingly lobate also, bending outward in broad, convex curves, where there are no natural barriers in the topography of the country to set it such a limit. Under these conditions such a lobate margin cannot belong to deposits of rivers, lakes, or ocean, but is precisely that which would mark the edge of a continental glacier
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