Part 2 — CHAPTER XXIV (continued 2)
Reading edition
The reason of the theoretical increase of summer heat being greater than the decrease of winter cold is because we are now nearest the sun in winter and farthest in summer, whereas we calculate the temperatures of the glacial epoch for the phase of precession when the aphelion was in winter. A large part of the increase of temperature would no doubt be used up in melting ice and evaporating water, so that there would be a much less increase of sensible heat; while only a portion of the theoretical lowering of temperature in winter would be actually produced owing to equalising effect of winds and currents, and the storing up of heat by the earth and ocean.
[46] Dr. Croll says this "is one of the most widespread and fundamental errors within the whole range of geological climatology." The temperature of the snow itself is, he says, one of the main factors. (Climate and Cosmology, p. 85.) But surely the temperature of the snow must depend on the temperature of the air through which it falls.
[47] In an account of Prof. Nordenskjöld's recent expedition round the northern coast of Asia, given in Nature, November 20th, 1879, we have the following passage, fully supporting the statement in the text. "Along the whole coast, from the White Sea to Behring's Straits, no glacier was seen. During autumn the Siberian coast is nearly free of ice and snow. There are no mountains covered all the year round with snow, although some of them rise to a height of more than 2,000 feet." It must be remembered that the north coast of Eastern Siberia is in the area of supposed greatest winter cold on the globe.
[48] Dr. Croll objects to this argument on the ground that Greenland and the Antarctic continent are probably lowlands or groups of islands. (Climate and Cosmology, Chap. V.)
[49] "On the Glacial Epoch," by James Croll. Geol. Mag. July, August, 1874.
[50] "The general absence of recent marks of glacial action in Eastern Europe is well known; and the series of changes which have been so well traced and described by Prof. Szabó as occurring in those districts seems to leave no room for those periodical extensions of 'ice-caps' with which some authors in this country have amused themselves and their readers. Mr. Campbell, whose ability to recognise the physical evidence of glaciers will scarcely be questioned, finds quite the same absence of the proof of extensive ice-action in North America, westward of the meridian of Chicago." (Prof. J. W. Judd in Geol. Mag. 1876, p. 535.)
The same author notes the diminution of marks of ice-action on going eastward in the Alps; and the Altai Mountains far in Central Asia show no signs of having been largely glaciated. West of the Rocky Mountains, however, in the Sierra Nevada and the coast ranges further north, signs of extensive old glaciers again appear; all which phenomena are strikingly in accordance with the theory here advocated, of the absolute dependence of glaciation on abundant rainfall and elevated snow-condensers and accumulators.
[51] I have somewhat modified this whole passage in the endeavour to represent more accurately the difference between the views of Dr. Croll and Sir Charles Lyell.
[52] For numerous details and illustrations see the paper—"On Ocean Currents in Relation to the Physical Theory of Secular Changes of Climate"—in the Philosophical Magazine, 1870.
[53] See Darwin's Naturalist's Voyage Round the World, 2nd Edition, pp. 244-251.
[54] The influence of geographical changes on climate is now held by many geologists who oppose what they consider the extravagant hypotheses of Dr. Croll. Thus, Prof. Dana imputes the glacial epoch chiefly, if not wholly, to elevation of the land caused by the lateral pressure due to shrinking of the earth's crust that has caused all other elevations and depressions. He says: "Now, that elevation of the land over the higher latitudes which brought on the glacial era is a natural result of the same agency, and a natural, and almost necessary, counterpart of the coral-island subsidence which must have been then in progress. The accumulating, folding, solidification, and crystallisation of rocks attending all the rock-making and mountain-making through the Palæozoic, Mesozoic, and Cenozoic eras, had greatly stiffened the crust in these parts; and hence in after times, the continental movements resulting from the lateral pressure necessarily appeared over the more northern portions of the continent, where the accumulations and other changes had been relatively small. To the subsidence which followed the elevation the weight of the ice-cap may have contributed in some small degree. But the great balancing movements of the crust of the continental and oceanic areas then going forward must have had a greatly preponderating effect in the oscillating agency of all time—lateral pressure within the crust." (American Journal of Science and Arts, 3rd Series, Vol. IX. p. 318.)
"In the 2nd edition of his Manual of Geology, Professor Dana suggests elevation of Arctic lands sufficient to exclude the Gulf Stream, as a source of cold during glacial epochs. This, he thinks, would have made an epoch of cold at any era of the globe. A deep submergence of Behring's Strait, letting in the Pacific warm current to the polar area, would have produced a mild Arctic climate like that of the Miocene period. When the warm current was shut out from the polar area it would yet reach near to it, and bring with it that abundant moisture necessary for glaciation." (Manual of Geology, 2nd Edition, pp. 541-755, 756.)
[55] Dana's Manual of Geology, 2nd Edition, p. 540.
[56] Dr. Croll says that I here assume an impossible state of things. He maintains "that the change from the distant sun in winter, and near sun in summer to the near sun in winter and distant sun in summer, aided by the change in the physical causes which this would necessarily bring about, would certainly be sufficient to cause the snow and ice to disappear." (Climate and Cosmology, p. 106.) But I demur to his "necessarily." It is not the direct effect of the nearer sun in winter that is supposed to melt the snow and ice, but the "physical causes," such as absence of fogs and increase of warm equatorial currents. But the near sun in winter acting on an ice-clad surface would only increase the fogs and snow, while the currents could only change if a large portion of the ice were first melted, in which case they would no doubt be modified so as to cause a further melting of the ice. Dr. Croll says: "The warm and equable conditions of climate which would then prevail, and the enormous quantity of intertropical water carried into the Southern Ocean, would soon produce a melting of the ice." (Loc. cit. p. 111.) This seems to me to be assuming the very point at issue. He has himself shown that the presence of large quantities of ice prevents "a warm and equable climate" however great may be the sun-heat; the ice therefore would not be melted, and there would be no increased flow of intertropical water to the Southern Ocean. The ocean currents are mainly due to the difference of temperature of the polar and equatorial areas combined with the peculiar form and position of the continents, and some one or more of these factors must be altered before the ocean currents towards the north pole can be increased. The only factor available is the Antarctic ice, and if this were largely increased, the northward-flowing currents might be so increased as to melt some of the Arctic ice. But the very same argument applies to both poles. Without some geographical change the Antarctic ice could not materially diminish during its winter in perihelion, nor increase to any important extent during the opposite phase. We therefore seem to have no available agency by which to get rid of the ice over a glaciated hemisphere, so long as the geographical conditions remained unchanged and the excentricity continued high.
[57] In the Geological Magazine, April, 1880, Mr. Searles V. Wood adduces what he considers to be the "conclusive objection" to Dr. Croll's excentricity theory, which is, that during the last glacial epoch Europe and North America were glaciated very much in proportion to their respective climates now, which are generally admitted to be due to the distribution of oceanic currents. But Dr. Croll admits his theory "to be baseless unless there was a complete diversion of the warm ocean currents from the hemisphere glaciated," in which case there ought to be no difference in the extent of glaciation in Europe and North America. Whether or not this is a correct statement of Dr. Croll's theory, the above objection certainly does not apply to the views here advocated; but as I also hold the "excentricity theory" in a modified form, it may be as well to show why it does not apply. In the first place I do not believe that the Gulf Stream was "completely diverted" during the glacial epoch, but that it was diminished in force, and (as described at p. 144) partly diverted southward. A portion of its influence would, however, still remain to cause a difference between the climates of the two sides of the Atlantic; and to this must be added two other causes—the far greater penetration of warm sea-water into the European than into the North American continent, and the proximity to America of the enormous ice-producing mass of Greenland. We have thus three distinct causes, all combining to produce a more severe winter climate on the west than on the east of the Atlantic during the glacial epoch, and though the first of these—the Gulf Stream—was not nearly so powerful as it is now, neither is the difference indicated by the ice-extension in the two countries so great as the present difference of winter-temperature, which is the essential point to be considered. The ice-sheet of the United States is usually supposed to have extended about ten, or, at most, twelve, degrees further south than it did in Western Europe, whereas we must go twenty degrees further south in the former country to obtain the same mean winter-temperature we find in the latter, as may be seen by examining any map of winter isothermals. This difference very fairly corresponds to the difference of conditions existing during the glacial epoch and the present time, so far as we are able to estimate them, and it certainly affords no grounds of objection to the theory by which the glaciation is here explained.
[58] Dr. Croll objects to this argument, and adduces the case of Greenland as showing that ice may accumulate far from sea. But the width of Greenland is small compared with that of the supposed Antarctic ice-cap. (Climate and Cosmology, p. 78.)
[59] The recent extensive glaciation of New Zealand is generally imputed by the local geologists to a greater elevation of the land; but I cannot help believing that the high phase of excentricity which caused our own glacial epoch was at all events an assisting cause. This is rendered more probable if taken in connection with the following very definite statement of glacial markings in South Africa. Captain Aylward in his Transvaal of To-day (p. 171) says:—"It will be interesting to geologists and others to learn that the entire country, from the summits of the Quathlamba to the junction of the Vaal and Orange rivers, shows marks of having been swept over, and that at no very distant period, by vast masses of ice from east to west. The striations are plainly visible, scarring the older rocks, and marking the hill-sides—getting lower and lower and less visible as, descending from the mountains, the kopjies (small hills) stand wider apart; but wherever the hills narrow towards each other, again showing how the vast ice-fields were checked, thrown up, and raised against their Eastern extremities."
This passage is evidently written by a person familiar with the phenomena of glaciation, and as Captain Aylward's preface is dated from Edinburgh, he has probably seen similar markings in Scotland. The country described consists of the most extensive and lofty plateau in South Africa, rising to a mountain knot with peaks more than 10,000 feet high, thus offering an appropriate area for the condensation of vapour and the accumulation of snow. At present, however, the mountains do not reach the snow-line, and there is no proof that they have been much higher in recent times, since the coast of Natal is now said to be rising. It is evident that no slight elevation would now lead to the accumulation of snow and ice in these mountains, situated as they are between 27° and 30° S. Lat.; since the Andes, which in 32° S. Lat. reach 23,300 feet high, and in 28° S. Lat. 20,000, with far more extensive plateaus, produce no ice-fields. We cannot, therefore, believe that a few thousand feet of additional elevation, even if it occurred so recently as indicated by the presence of striations, would have produced the remarkable amount of glaciation above described; while from the analogy of the northern hemisphere, we may well believe that it was mainly due to the same high excentricity that led to the glaciation of Western and Central Europe, and Eastern North America.
These observations confirm those of Mr. G. W. Stow, who, in a paper published in the Quarterly Journal of the Geological Society (Vol. XXVII. p. 539), describes similar phenomena in the same mountains, and also mounds and ridges of unstratified clay packed with angular boulders; while further south the Stormberg mountains are said to be similarly glaciated, with immense accumulations of morainic matter in all the valleys. We have here most of the surface phenomena characteristic of a glaciated country, only a few degrees south of the tropic; and taken in connection with the indications of recent glaciation in New Zealand, and those discovered by Dr. R. von Lendenfeld in the Australian Alps between 6,000 and 7,000 feet elevation (Nature, Vol. XXXII. p. 69), we can hardly doubt the occurrence of some general and wide-spread cause of glaciation in the southern hemisphere at a period so recent that the superficial phenomena are almost as well preserved as in Europe. Other geologists however deny that there are any distinct indications of glacial action in South Africa; but the recent discovery by Dr. J. W. Gregory, F.G.S., of the former extension of glaciers on Mount Kenya 5,000 feet below their present limits, renders probable the former glaciation of the South African Highlands.
[60] The astronomical facts connected with the motions and appearance of the planet are taken from a paper by Mr. Edward Carpenter, M.A., in the Geological Magazine of March, 1877, entitled, "Evidence Afforded by Mars on the Subject of Glacial Periods," but I arrive at somewhat different conclusions from those of the writer of the paper.
[61] In an article in Nature of Jan. 1, 1880, the Rev. T. W. Webb states that in 1877 the pole of Mars (? the south pole) was, according to Schiaparelli, entirely free of snow. He remarks also on the regular contour of the supposed snows of Mars as offering a great contrast to ours, and also the strongly marked dark border which has often been observed. On the whole Mr. Webb seems to be of opinion that there can be no really close resemblance between the physical condition of the Earth and Mars, and that any arguments founded on such supposed similarity are therefore untrustworthy.
[62] London, Edinburgh and Dublin Philosophical Magazine, Vol. XXXVI., pp. 144-150 (1868).
[63] Climate and Time in their Geological Relations, p. 341.
[64] Nature, Vol. XXI., p. 345, "The Interior of Greenland."
[65] Prof. J. W. Judd says: "In the case of the Alps I know of no glacial phenomena which are not capable of being explained, like those of New Zealand, by a great extension of the area of the tracts above the snow-line which would collect more ample supplies for the glaciers protruded into surrounding plains. And when we survey the grand panoramas of ridges, pinnacles, and peaks produced for the most part by sub-aërial action, we may well be prepared to admit that before the intervening ravines and valleys were excavated, the glaciers shed from the elevated plateaux must have been of vastly greater magnitude than at present." (Contributions to the Study of Volcanoes, Geological Magazine, 1876, p. 536.) Professor Judd applies these remarks to the last as well as to previous glacial periods in the Alps; but surely there has been no such extensive alteration and lowering of the surface of the country since the erratic blocks were deposited on the Jura and the great moraines formed in North Italy, as this theory would imply. We can hardly suppose wide areas to have been lowered thousands of feet by denudation, and yet have left other adjacent areas apparently untouched; and it is even very doubtful whether such an extension of the snow-fields would alone suffice for the effects which were certainly produced.
[66] Geological Magazine, 1876, p. 392.
[67] Colonel Fielden thinks that these trees have all been brought down by rivers, and have been stranded on shores which have been recently elevated. See Trans. of Norfolk Nat. Hist. Soc., Vol. III., 1880.
[68] Geological Magazine, 1876, "Geology of Spitzbergen," p. 267.
[69] The preceding account is mostly derived from Professor Heer's great work Flora Fossilis Arctica.
[70] Geological Magazine, 1875, p. 531.
[71] Geological Magazine, 1876, p. 266. In his recent work—Climate and Cosmology (pp. 164, 172)—the late Dr. Croll has appealed to the imperfection of the geological record as a reply to these arguments; in this case, as it appears to me, a very unsuccessful one.
[72] It is interesting to observe that the Cretaceous flora of the United States (that of the Dakota group), indicates a somewhat cooler climate than that of the following Eocene period. Mr. De Rance (in the geological appendix to Capt. Sir G. Nares's Narrative of a Voyage to the Polar Sea) remarks as follows: "In the overlying American Eocenes occur types of plants occurring in the European Miocenes and still living, proving the truth of Professor Lesquereux's postulate, that the plant types appear in America a stage in advance of their advent in Europe. These plants point to a far higher mean temperature than those of the Dakota group, to a dense atmosphere of vapour, and a luxuriance of ferns and palms." This is very important as adding further proof to the view that the climates of former periods are not due to any general refrigeration, but to causes which were subject to change and alternation in former ages as now.
[73] Mr. S. B. J. Skertchley informs me that he has himself observed thick Tertiary deposits, consisting of clays and anhydrous gypsum, at Berenice on the borders of Egypt and Nubia, at a height of about 600 feet above the sea-level; but these may have been of fresh-water origin.
[74] By referring to our map of the Indian Ocean showing the submarine banks indicating ancient islands (Chap. XIX.), it will be evident that the south-east trade-winds—then exceptionally powerful—would cause a vast body of water to enter the deep Arabian Sea.
[75] In his recently published Lectures on Physical Geography, Professor Haughton calculates, that more than half the solar heat of the torrid zone is carried to the temperate zones by ocean currents. The Gulf Stream itself carries one-twelfth of the total amount, but it is probable that a very small fraction of this quantity of heat reaches the polar seas owing to the wide area over which the current spreads in the North Atlantic. The corresponding stream of the Indian Ocean in Miocene times would have been fully equal to the Gulf Stream in heating power, while, owing to its being so much more concentrated, a large proportion of its heat may have reached the polar area. But the Arctic Ocean occupies less than one-tenth of the area of the tropical seas; so that, whatever proportion of the heat of the tropical zone was conveyed to it, would, by being concentrated into one-tenth of the surface, produce an enormously increased effect. Taking this into consideration, we can hardly doubt that the opening of a sufficient passage from the Indian Ocean to the Arctic seas would produce the effects above indicated.
[76] For an account of the resemblances and differences of the mammalia of the two continents during the Tertiary epoch, see my Geographical Distribution of Animals, Vol. I. pp. 140-156.
[77] Professor Haughton has made an elaborate calculation of the difference between existing climates and those of Miocene times, for all the places where a Miocene flora has been discovered, by means of the actual range of corresponding species and genera of plants. Although this method is open to the objection that the ranges of plants and animals are not determined by temperature only, yet the results may be approximately correct, and are very interesting. The following table which summarizes these results is taken from his Lectures on Physical Geography (p. 344):—
Latitude. Present Temperature. Miocene Temperature. Difference.
1. Switzerland 47°.00 53°.6 F 69°.8 F 16°.2 F
2. Dantzig 54°.21 45°.7 ,, 62°.6 ,, 16°.9 ,,
3. Iceland 65°.30 35°.6 ,, 48°.2 ,, 12°.6 ,,
4. Mackenzie River 65°.00 19°.4 ,, 48°.2 ,, 28°.8 ,,
5. Disco (Greenland) 70°.00 19°.6 ,, 55°.6 ,, 36°.0 ,,
6. Spitzbergen 78°.00 16°.5 ,, 51°.8 ,, 35°.3 ,,
7. Grinnell Land 81°.44 1°.7 ,, 42°.3 ,, 44°.0 ,,
It is interesting to note that Iceland, which is now exposed to the full influence of the Gulf Stream, was only 12°.6 F. warmer in Miocene times, while Mackenzie River, now totally removed from its influence was 28° warmer. This, as well as, the greater increase of temperature as we go northward and the polar area becomes more limited, is quite in accordance with the view of the causes which brought about the Miocene climate which is here advocated.
[78] The objection has been made, that the long polar night would of itself be fatal to the existence of such a luxuriant vegetation as we know to have existed as far as 80° N. Lat., and that there must have been some alteration of the position of the pole, or diminution of the obliquity of the ecliptic, to permit such plants as magnolias and large-leaved maples to flourish. But there appears to be really no valid grounds for such an objection. Not only are numbers of Alpine and Arctic evergreens deeply buried in the snow for many months without injury, but a variety of tropical and sub-tropical plants are preserved in the hot-houses of St. Petersburg and other northern cities, which are closely matted during winter, and are thus exposed to as much darkness as the night of the Arctic regions. We have besides no proof that any of the Arctic trees or large shrubs were evergreens, and the darkness would certainly not be prejudical to deciduous plants. With a suitable temperature there is nothing to prevent a luxuriant vegetation up to the pole, and the long continued day is known to be highly favourable to the development of foliage, which in the same species is larger and better developed in Norway than in the south of England.
[79] Geological Magazine, 1873, p. 320.
[80] Geological Magazine, 1877, p. 137.
[81] Manual of Geology, 2nd Ed. p. 525. See also letter in Nature, Vol. XXIII. p. 410.
[82] Nature, Vol. XVIII. (July, 1878), p. 268.
[83] "On the Comparative Value of certain Geological Ages considered as items of Geological Time." (Proceedings of the Royal Society, 1874, p. 334.)
[84] Trans. Royal Society of Edinburgh, Vol. XXIII. p. 161. Quarterly Journal of Science, 1877. (Croll on the "Probable Origin and Age of the Sun.")
[85] Philosophical Magazine, April, 1853.
[86] It has usually been the practice to take the amount of denudation in the Mississippi valley, or one foot in six thousand years, as a measure of the rate of denudation in Europe, from an idea apparently of being on the "safe side," and of not over-estimating the rate of change. But this appears to me a most unphilosophical mode of proceeding and unworthy of scientific inquiry. What should we think of astronomers if they always took the lowest estimates of planetary or stellar distances, instead of the mean results of observation, "in order to be on the safe side!"? As if error in one direction were any worse than error in another. Yet this is what geologists do systematically. Whenever any calculations are made involving the antiquity of man, it is those that give the lowest results that are always taken, for no reason apparently except that there was, for so long a time, a prejudice, both popular and scientific, against the great antiquity of man; and now that a means has been found of measuring the rate of denudation, they take the slowest rate instead of the mean rate, apparently only because there is now a scientific prejudice in favour of extremely slow geological change. I take the mean of the whole; and as this is almost exactly the same as the mean of the three great European rivers—the Rhone, Danube, and Po—I cannot believe that this will not be nearer the truth for Europe than taking one North American river as the standard.
[87] "On the Height of the Land and the Depth of the Ocean," in the Scottish Geographical Magazine, 1888.
[88] These figures are merely used to give an idea of the rate at which denudation is actually going on now; but if no elevatory forces were at work, the rate of denudation would certainly diminish as the mountains were lowered and the slope of the ground everywhere rendered flatter. This would follow not only from the diminished power of rain and rivers, but because the climate would become more uniform, the rainfall probably less, and no rocky peaks would be left to be fractured and broken up by the action of frosts. It is certain, however, that no continent has ever remained long subject to the influences of denudation alone, for, as we have seen in our sixth chapter, elevation and depression have always been going on in one part or other of the surface.
[89] The following statement of the depths at which the Palæozoic formations have been reached in various localities in and round London was given by Mr. H. B. Woodward in his address to the Norwich Geological Society in 1879:—
Deep Wells through the Tertiary and Cretaceous Formations.
Harwich at 1,022 feet reached Carboniferous Rock.
Kentish Town ,, 1,114 ,, ,, Old Red Sandstone.
Tottenham Court Road ,, 1,064 ,, ,, Devonian.
Blackwall ,, 1,004 ,, ,, Devonian or Old Red Sandstone.
Ware ,, 800 ,, ,, Silurian (Wenlock Shale).
We thus find that over a wide area, extending from London to Ware and Harwich, the whole of the formations from the Oolite to the Permian are wanting, the Cretaceous resting on the Carboniferous or older Palæozoic rocks; and the same deficiency extends across to Belgium, where the Tertiary beds are found resting on Carboniferous at a depth of less than 400 feet.
[90] Geological Magazine, Vol. VIII., March, 1871.
[91] Mr. C. Lloyd Morgan has well illustrated this point by comparing the generally tilted-up strata denuded on their edges, to a library in which a fire had acted on the exposed edges of the books, destroying a great mass of literature but leaving a portion of each book in its place, which portion represents the thickness but not the size of the book. (Geological Magazine, 1878, p. 161.)
[92] Professor J. Young thinks it highly probable that—"the Lower Greensand is contemporaneous with part of the Chalk, so were parts of the Wealden; nay, even of the Purbeck a portion must have been forming while the Cretaceous sea was gradually deepening southward and westward." Yet these deposits are always arranged successively, and their several thicknesses added together to obtain the total thickness of the formations of the country. (See Presidential Address, Sect. C. British Association, 1876.)
[93] Mr. John Murray in his more careful estimate makes it about 51½ millions.
[94] As by far the larger portion of the denuded matter of the globe passes to the sea through comparatively few great rivers, the deposits must often be confined to very limited areas. Thus the denudation of the vast Mississippi basin must be almost all deposited in a limited portion of the Gulf of Mexico, that of the Nile within a small area of the Eastern Mediterranean, and that of the great rivers of China—the Hoang Ho and Yang-tse-kiang, in a small portion of the Eastern Sea. Enormous lengths of coast, like those of Western America and Eastern Africa, receive very scanty deposits; so that thirty miles in width along the whole of the coasts of the globe will probably give an area greater than that of the area of average deposit, and certainly greater than that of maximum deposit, which is the basis on which I have here made my estimates. In the case of the Mississippi, it is stated by Count Pourtales that along the plateau between the mouth of the river and the southern extremity of Florida for two hundred and fifty miles in width the bottom consists of clay with some sand and but few Rhizopods; but beyond this distance the soundings brought up either Rhizopod shells alone, or these mixed with coral sand, Nullipores, and other calcareous organisms (Dana's Manual of Geology, 2nd Ed. p. 671). It is probable, therefore, that a large proportion of the entire mass of sediment brought down by the Mississippi is deposited on the limited area above indicated.
Professor Dana further remarks: "Over interior oceanic basins as well as off a coast in quiet depths, fifteen or twenty fathoms and beyond, the deposits are mostly of fine silt, fitted for making fine argillaceous rocks, as shales or slates. When, however, the depth of the ocean falls off below a hundred fathoms, the deposition of silt in our existing oceans mostly ceases, unless in the case of a great bank along the border of a continent."
[95] From the same data Professor Haughton estimates a minimum of 200 million years for the duration of geological time; but he arrives at this conclusion by supposing the products of denudation to be uniformly spread over the whole sea-bottom instead of over a narrow belt near the coasts, a supposition entirely opposed to all the known facts, and which had been shown by Dr. Croll, five years previously, to be altogether erroneous. (See Nature, Vol. XVIII., p. 268, where Professor Haughton's paper is given as read before the Royal Society.)
[96] See Geological Magazine for 1877, p. 1.
[97] In his reply to Sir W. Thomson, Professor Huxley assumed one foot in a thousand years as a not improbable rate of deposition. The above estimate indicates a far higher rate; and this follows from the well-ascertained fact, that the area of deposition is many times smaller than the area of denudation.
[98] Dr. Croll and Sir Archibald Geikie have shown that marine denudation is very small in amount as compared with sub-aërial, since it acts only locally on the edge of the land, whereas the latter acts over every foot of the surface. Mr. W. T. Blanford argues that the difference is still greater in tropical than in temperate latitudes, and arrives at the conclusion that—"If over British India the effects of marine to those of fresh-water denudation in removing the rocks of the country be estimated at 1 to 100, I believe that the result of marine action will be greatly overstated" (Geology and Zoology of Abyssinia, p. 158, note). Now, as our estimate of the rate of sub-aërial denudation cannot pretend to any precise accuracy, we are justified in neglecting marine denudation altogether, especially as we have no method of estimating it for the whole earth with any approach to correctness.
[99] Agassiz appears to have been the first to suggest that the principal epochs of life extermination were epochs of cold; and Dana thinks that two at least such epochs may be recognised, at the close of the Palæozoic and of the Cretaceous periods—to which we may add the last glacial epoch.
[100] This view was, I believe, first put forth by myself in a paper read before the Geological Section of the British Association in 1869, and subsequently in an article in Nature, Vol. I. p. 454. It was also stated by Mr. S. B. J. Skertchley in his Physical System of the Universe, p. 363 (1878); but we both founded it on what I now consider the erroneous doctrine that actual glacial epochs recurred each 10,500 years during periods of high excentricity.
[101] Explication d'une seconde édition de la Carte Géologique de la Terre (1875), p. 64.
[102] For most of the facts as to the zoology and botany of these islands, I am indebted to Mr. Godman's valuable work—Natural History of the Azores or Western Islands, by Frederick Du Cane Godman, F.L.S., F.Z.S., &c., London, 1870.
[103] See Chap. V. p. 78.
[104] Some of Mr. Darwin's experiments are very interesting and suggestive. Ripe hazel-nuts sank immediately, but when dried they floated for ninety days, and afterwards germinated. An asparagus-plant with ripe berries, when dried, floated for eighty-five days, and the seeds afterwards germinated. Out of ninety-four dried plants experimented with, eighteen floated for more than a month, and some for three months, and their powers of germination seem never to have been wholly destroyed. Now, as oceanic currents vary from thirty to sixty miles a day, such plants under the most favourable conditions might be carried 90 X 60 = 5,400 miles! But even half of this is ample to enable them to reach any oceanic island, and we must remember that till completely water-logged they might be driven along at a much greater rate by the wind. Mr. Darwin calculates the distance by the average time of flotation to be 924 miles; but in such a case as this we are entitled to take the extreme cases, because such countless thousands of plants and seeds must be carried out to sea annually that the extreme cases in a single experiment with only ninety-four plants, must happen hundreds or thousands of times and with hundreds or thousands of species, naturally, and thus afford ample opportunities for successful migration. (See Origin of Species, 6th Edition, p. 325.)
[105] The following remarks, kindly communicated to me by Mr. H. N. Moseley, naturalist to the Challenger, throw much light on the agency of birds in the distribution of plants:—"Grisebach (Veg. der Erde, Vol. II. p. 496) lays much stress on the wide ranging of the albatross (Diomedea) across the equator from Cape Horn to the Kurile Islands, and thinks that the presence of the same plants in Arctic and Antarctic regions may be accounted for, possibly, by this fact. I was much struck at Marion Island of the Prince Edward group, by observing that the great albatross breeds in the midst of a dense, low herbage, and constructs its nest of a mound of turf and herbage. Some of the indigenous plants, e.g. Acæna, have flower-heads which stick like burrs to feathers, &c., and seem specially adapted for transposition by birds. Besides the albatrosses, various species of Procellaria and Puffinus, birds which range over immense distances may, I think, have played a great part in the distribution of plants, and especially account, in some measure, for the otherwise difficult fact (when occurring in the tropics), that widely distant islands have similar mountain plants. The Procellaria and Puffinus in nesting, burrow in the ground, as far as I have seen choosing often places where the vegetation is the thickest. The birds in burrowing get their feathers covered with vegetable mould, which must include spores, and often seeds. In high latitudes the birds often burrow near the sea-level, as at Tristan d'Acunha or Kerguelen's Land, but in the tropics they choose the mountains for their nesting-place (Finsch and Hartlaub, Orn. der Viti- und Tonga-Inseln, 1867, Einleitung, p. xviii.). Thus, Puffinus megasi nests at the top of the Korobasa basaga mountain, Viti Levu, fifty miles from the sea. A Procellaria breeds in like manner in the high mountains of Jamaica, I believe at 7,000 feet. Peale describes the same habit of Procellaria rostrata at Tahiti, and I saw the burrows myself amidst a dense growth of fern, &c., at 4,400 feet elevation in that island. Phaethon has a similar habit. It nests at the crater of Kilauea, Hawaii, at 4,000 feet elevation, and also high up in Tahiti. In order to account for the transportation of the plants, it is not of course necessary that the same species of Procellaria or Diomedea should now range between the distant points where the plants occur. The ancestor of the now differing species might have carried the seeds. The range of the genus is sufficient."
[106] Nature, Vol. VI. p. 262, "Recent Observations in the Bermudas," by Mr. J. Matthew Jones.
[107] "The late Sir C. Wyville Thomson was of opinion that the 'red earth' which largely forms the soil of Bermuda had an organic origin, as well as the 'red clay' which the Challenger discovered in all the greater depths of the ocean basins. He regarded the red earth and red clay as an ash left behind after the gradual removal of the lime by water charged with carbonic acid. This ash he regarded as a constituent part of the shells of Foraminifera, skeletons of Corals, and Molluscs, [vide Voyage of the Challenger, Atlantic, Vol. I. p. 316]. This theory does not seem to be in any way tenable. Analysis of carefully selected shells of Foraminifera, Heteropods, and Pteropods, did not show the slightest trace of alumina, and none has as yet been discovered in coral skeletons. It is most probable that a large part of the clayey matter found in red clay and the red earth of Bermuda is derived from the disintegration of pumice, which is continually found floating on the surface of the sea. [See Murray, "On the Distribution of Volcanic Débris Over the Floor of the Ocean;" Proc. Roy. Soc. Edin. Vol. IX. pp. 247-261. 1876-1877.] The naturalists of the Challenger found it among the floating masses of gulf weed, and it is frequently picked up on the reefs of Bermuda and other coral islands. The red earth contains a good many fragments of magnetite, augite, felspar, and glassy fragments, and when a large quantity of the rock of Bermuda is dissolved away with acid, a small number of fragments are also met with. These mineral particles most probably came originally from the pumice which had been cast up on the island for long ages (for it is known that these minerals are present in pumice), although possibly some of them may have come from the volcanic rock, which is believed to form the nucleus of the island." The Voyage of H.M.S. Challenger, Narrative of the Cruise, Vol. I. 1885, pp. 141-142.
[108] Four bats occur rarely, two being N. American, and two West Indian Species. The Bermuda Islands, by Angelo Heilprin, Philadelphia, 1889.
[109] Fourteen species of Spiders were collected by Prof. A. Heilprin, all American or cosmopolitan species except one, Lycosa atlantica, which Dr. Marx of Washington describes as new and as peculiar to the islands. (Heilprin's The Bermudas, p. 93.)
[110] Mr. Theo. D. A. Cockerell informs me that there are two slugs in Bermuda of which specimens exist in the British Museum,—Amalia gagates Drap. common in Europe, and Agriolimax campestris of the United States. Both may therefore have been introduced by human agency. Also Vaginulus Morelete var. schivelyæ which seems to be a variety of a Mexican species; perhaps imported.
[111] "Notes on the Vegetation of Bermuda," by H. N. Moseley. (Journal of the Linnean Society, Vol. XIV., Botany, p. 317.)
[112] Gigantic Land Tortoises Living and Extinct in the Collection of the British Museum. By A. C. L. G. Günther, F.R.S. 1877.
[113] The following list of the beetles yet known from the Galapagos shows their scanty proportions and accidental character; the forty species belonging to thirty-three genera and eighteen families. It is taken from Mr. Waterhouse's enumeration in the Proceedings of the Zoological Society for 1877 (p. 81), with a few additions collected by the U. S. Fish Commission Steamer Albatross, and published by the U. S. National Museum in 1889.
Carabidæ. Feronia calathoides. ,, insularis. ,, galapagoensis. Amblygnathus obscuricornis. Solenophorus galapagoensis. Notaphus galapagoensis. Dytiscidæ. Eunectes occidentalis. Acilius incisus. Copelatus galapagoensis. Palpicornes. Tropisternus lateralis. Philhydrus sp. Staphylinidæ. Creophilus villosus. Necrophaga. Acribis serrativentris. Phalacrus darwinii. Dermestes vulpinus. Malacoderms. Ablechrus darwinii. Corynetes rufipes. Bostrichus unciniatus. Tetrapriocerca sp. Lamellicornes. Copris lugubris. Oryctes galapagoensis. Elateridæ. Physorhinus galapagoensis Heteromera. Allecula n. s. Stomion helopoides. ,, lævigatum. Ammophorus obscurus. ,, cooksoni. ,, bifoveatus. Pedonœces galapagoensis. ,, pubescens. Phaleria manicata. Curculionidæ. Otiorhynchus cuneiformis. Anchonus galapagoensis. Longicornia. Mallodou sp. Eburia amabilis. Anthribidæ. Ormiscus variegatus. Phytophaga. Diabrotica limbata. Docema galapagoensis. Longitarsus lunatus. Securipalpes. Scymuns galapagoensis.
[114] Mr. H. O. Forbes, who visited these islands in 1878, increased the number of wild plants to thirty-six, and these belonged to twenty-six natural orders.
[115] Juan Fernandez is a good example of a small island which, with time and favourable conditions, has acquired a tolerably rich and highly peculiar flora and fauna. It is situated in 34° S. Lat., 400 miles from the coast of Chile, and so far as facilities for the transport of living organisms are concerned is by no means in a favourable position, for the ocean-currents come from the south-west in a direction where there is no land but the Antarctic continent, and the prevalent winds are also westerly. No doubt, however, there are occasional storms, and there may have been intermediate islands, but its chief advantages are its antiquity, its varied surface, and its favourable soil and climate, offering many chances for the preservation and increase of whatever plants and animals have chanced to reach it. The island consists of basalt, greenstone, and other ancient rocks, and though only about twelve miles long its mountains are three thousand feet high. Enjoying a moist and temperate climate it is especially adapted to the growth of ferns, which are very abundant; and as the spores of these plants are as fine as dust, and very easily carried for enormous distances by winds, it is not surprising that there are nearly fifty species on the island, while the remote period when it first received its vegetation may be indicated by the fact that nearly half the species are quite peculiar; while of 102 species of flowering plants seventy are peculiar, and there are ten peculiar genera. The same general character pervades the fauna. For so small an island it is rich, containing four true land-birds, about fifty species of insects, and twenty of land-shells. Almost all these belong to South American genera, and a large proportion are South American species; but several of the insects, half the birds, and the whole of the land-shells are peculiar. This seems to indicate that the means of transmission were formerly greater than they are now, and that in the case of land-shells none have been introduced for so long a period that all have become modified into distinct forms, or have been preserved on the island while they have become extinct on the continent. For a detailed examination of the causes which have led to the modification of the humming birds of Juan Fernandez see the chapter on Humming Birds in the author's Natural Selection and Tropical Nature, p. 324; while a general account of the fauna of the island is given in his Geographical Distribution of Animals, Vol. II. p. 49.
[116] No additions appear to have been made to this flora down to 1885, when Mr. Hemsley published his Report on the Present State of our Knowledge of Insular Floras.
[117] Journal of the Linnean Society, Vol. XIII., "Botany," p. 556.
[118] Geographical Distribution of Animals, Vol. II. p. 81.
[119] St. Helena: a Physical, Historical, and Topographical Description of the Island, &c. By John Charles Melliss, F.G.S., &c. London: 1875.
[120] Mr. Marsh in his interesting work entitled The Earth as Modified by Human Action (p. 51), thus remarks on the effect of browsing quadrupeds in destroying and checking woody vegetation.—"I am convinced that forests would soon cover many parts of the Arabian and African deserts if man and domestic animals, especially the goat and the camel, were banished from them. The hard palate and tongue, and strong teeth and jaws of this latter quadruped enable him to break off and masticate tough and thorny branches as large as the finger. He is particularly fond of the smaller twigs, leaves, and seed-pods of the Sont and other acacias, which, like the American robinia, thrive well on dry and sandy soils, and he spares no tree the branches of which are within his reach, except, if I remember right, the tamarisk that produces manna. Young trees sprout plentifully around the springs and along the winter water-courses of the desert, and these are just the halting stations of the caravans and their routes of travel. In the shade of these trees annual grasses and perennial shrubs shoot up, but are mown down by the hungry cattle of the Bedouin as fast as they grow. A few years of undisturbed vegetation would suffice to cover such points with groves, and these would gradually extend themselves over soils where now scarcely any green thing but the bitter colocynth and the poisonous foxglove is ever seen."
[121] Coleoptera Sanctæ Helenæ, 1877; Testacea Atlantica, 1878.
[122] On Petermann's map of Africa, in Stieler's Hand-Atlas (1879), the Island of Ascension is shown as seated on a much larger and shallower submarine bank than St. Helena. The 1,000 fathom line round Ascension encloses an oval space 170 miles long by 70 wide, and even the 300 fathom line, one over 60 miles long; and it is therefore probable that a much larger island once occupied this site. Now Ascension is nearly equidistant between St. Helena and Liberia, and such an island might have served as an intermediate station through which many of the immigrants to St. Helena passed. As the distances are hardly greater than in the case of the Azores, this removes whatever difficulty may have been felt of the possibility of any organisms reaching so remote an island. The present island of Ascension is probably only the summit of a huge volcanic mass, and any remnant of the original fauna and flora it might have preserved may have been destroyed by great volcanic eruptions. Mr. Darwin collected some masses of tufa which were found to be mainly organic, containing, besides remains of fresh-water infusoria, the siliceous tissue of plants! In the light of the great extent of the submarine bank on which the island stands, Mr. Darwin's remark, that—"we may feel sure, that at some former epoch, the climate and productions of Ascension were very different from what they are now,"—has received a striking confirmation. (See Naturalist's Voyage Round the World, p. 495.)
[123] "Notes on the Classification, History, and Geographical Distribution of Compositæ."—Journal of the Linnean Society, Vol. XIII. p. 563 (1873).
[124] The Melhaniæ comprise the two finest timber trees of St. Helena, now almost extinct, the redwood and native ebony.
[125] Journal of the Linnean Society, 1873, p. 496. "On Diversity of Evolution under one set of External Conditions." Proceedings of the Zoological Society of London, 1873, p. 80. "On the Classification of the Achitinellidæ."
[126] "Memoirs on the Coleoptera of the Hawaiian Islands." By the Rev. T. Blackburn, B.A., and Dr. D. Sharp. Scientific Transactions of the Royal Dublin Society. Vol. III. Series II. 1885.
[127] See Hildebrand's Flora of the Hawaiian Islands, Introduction, p. xiv.
[128] Flora of the Hawaiian Islands, by W. Hildebrand, M.D., annotated and published after the author's death by W. F. Hildebrand, 1888.
[129] These are obtained from Hildebrand's Flora supplemented by Mr. Bentham's paper in the Journal of the Linnean Society.
[130] Among the curious features of the Hawaiian flora is the extraordinary development of what are usually herbaceous plants into shrubs or trees. Three species of Viola are shrubs from three to five feet high. A shrubby Silene is nearly as tall; and an allied endemic genus, Schiedea, has numerous shrubby species. Geranium arboreum is sometimes twelve feet high. The endemic Compositæ are mostly shrubs, while several are trees reaching twenty or thirty feet in height. The numerous Lobeliaceæ, all endemic, are mostly shrubs or trees, often resembling palms or yuccas in habit, and sometimes twenty-five or thirty feet high. The only native genus of Primulaceæ—Lysimachia—consists mainly of shrubs; and even a plantain has a woody stem sometimes six feet high.
[131] Geological Magazine, 1870, p. 155.
[132] Transactions of the Edinburgh Geological Society, Vol. I. p. 330.
[133] Quarterly Journal of Geological Society, 1850, p. 96.
[134] British Association Report, Dundee, 1867, p. 431.
[135] The list of names was furnished to me by Dr. Günther, and I have added the localities from the papers containing the original descriptions, and from Dr. Haughton's British Freshwater Fishes.
[136] See "The Virginia Colony of Helix nemoralis," T. D. A. Cockerell, in The Nautilus, Vol. III. No. 7, p. 73.
[137] I am indebted to Mr. Mitten for this curious fact.
[138] The following remarks by Dr. Richard Spruce, who has made a special study of mosses and especially of hepaticæ, are of interest. "From what precedes, I conclude that no existing agency is capable of transporting the germs of our hepatics of tropical type from the torrid zone to Britain, and I venture to suppose that their existence at Killarney dates from the remote period when the vegetation of the whole northern hemisphere partook of a tropical character. If I am challenged to account for their survival through the last glacial period, I reply that, granting even the existence of a universal ice-cap down to the latitude of 40° in America and 50° in Europe, it is not to be assumed that the whole extent, even of land, was perennially entombed 'in thrilling regions of thick-ribbed ice.' Towards the southern margin of the ice the climate was probably very similar to that of Greenland and the northern part of Norway at the present day. The summer sun would have great power, and on the borders of sheltered fjords the frozen snow would disappear completely, if only for a very short period, and I ask only for a month or two, not doubting the capacity of our hepatics to survive in a dormant state under the snow for at least ten months in the year. I have gathered mosses in the Pyrenees where the snow had barely left them on August 2nd; by September 25th they were re-covered with snow, and would not be again uncovered till the following year. The mosses of Killarney might even enjoy a longer summer than this; for the gulf-stream laves both sides of the south-western angle of Ireland, and its tepid waters would exert great melting power on the ice-bound coast, preventing at the same time any formation of ice in the sea itself." This passage is the conclusion of a very interesting discussion on the distribution of hepaticæ in a paper on "A New Hepatic from Killarney," in the Journal of Botany, vol. 25, (Feb. 1887), pp. 33-82, in which many curious facts are given as to the habits and distribution of these curious and beautiful little plants.
[139] While these pages are passing through the press I am informed by my friend Mr. W. H. Beeby that in the Shetland Isles, where he has been collecting for five summers, he has found several plants new to the British flora, and a few altogether undescribed. Among these latter is a very distinct species of Hieracium (H. Zetlandicum), which is quite unknown in Scandinavia, and is almost certainly peculiar to the British Islands. Here we have another proof that entirely new species are still to be discovered in the remoter portions of our country.
[140] In the first edition of this work the numbers were 400 and 340, showing the great increase of our knowledge during the last ten years, chiefly owing to the researches of Mr. A. H. Everett in Sarawak and Mr. John Whitehead in North Borneo and the great mountain Kini Balu.
[141] These are Allocotops, Chlorocharis, Androphilus, and Ptilopyga, among the Timeliidæ; Tricophoropsis and Oreoctistes among the Brachypodidæ; Chlamydochœra among the Campophagidæ.
[142] In a letter from Darwin he says:—"Hooker writes to me, 'Miguel has been telling me that the flora of Sumatra and Borneo are identical, and that of Java quite different.'"
[143] "On the Geology of Sumatra," by M. R. D. M. Verbeck. Geological Magazine, 1877.
[144] Pitta megarhynchus (Banca) allied to P. brachyurus (Borneo, Sumatra, Malacca); and Pitta bangkanus (Banca) allied to P. sordidus (Borneo and Sumatra).
[145] The following list of the mammalia of the Philippines and the Sulu Islands has been kindly furnished me by Mr. Everett.
Quadrumana. 1. Macacus cynomolgus. 2. Tarsius spectrum. Carnivora. 3. Viverra tangalunga. 4. Paradoxurus philippinensis. Also in Palawan. 5. Felis bengalensis. In Negros Island. Ungulata. 6. Bubalus mindorensis. Peculiar species. 7. Cervus philippinus. Peculiar species. 8. ,, alfredi. Peculiar species. 9. ,, nigricans. Peculiar species. 10. ,, pseudaxis. Sulu only. Probably introduced. 11. Sus marchesi. Peculiar species. Rodentia. 12. Sciurus philippinensis. Peculiar species. 13. ,, cagos. Peculiar species. 14. ,, concinnus. Peculiar. Mindanao and Basilan. 15. Phlæomys cummingi. Peculiar genus. 16. Mus ephippium. 17. ,, everetti. Peculiar species. Insectivora. 18. Crocidura luzoniensis. Peculiar species. 19. ,, edwardsiana. Peculiar species. 20. Dendrogale sp. 21. Galeopithecus philippinensis. Peculiar species. Chiroptera. 22. Pteropus leucopterus. 23. ,, edulis. 24. ,, hypomelanus. 25. ,, jubatus. 26. Xantharpyia amplexicaule. 27. Cynopterus marginatus. 28. ,, jagorii. Peculiar species. 29. Carponycteris australis. 30. Rhinolophus luctus. 31. ,, philippinensis. Peculiar species. 32. ,, rufus. Peculiar species. 33. Hipposideros diadema. 34. ,, pygmæus. Peculiar species. 35. ,, larvatus. 36. ,, obscurus. Peculiar species. 37. ,, coronatus. Peculiar species. 38. ,, bicolor. 39. Megaderma spasma. 40. Vesperugo pachypus. 41. ,, tenuis. 42. ,, abramus. 43. Nycticejus kuhlii. 44. Vespertilio macrotarsus. Peculiar species. 45. ,, capaccinii. 46. Harpiocephalus cyclotis. 47. Kerivoula hardwickii. 48. ,, pellucida. Peculiar species. 49. ,, jagorii. Peculiar species. 50. Miniopterus schreibersii. 51. ,, tristis. Peculiar species. 52. Emballonura monticola. 53. Taphyzous melanopogon. 54. Nyctinomus plicatus.
[146] Extracted from Messrs. Blakiston and Pryer's Catalogue of Birds of Japan (Ibis, 1878, p. 209), with Mr. Seebohm's additions and corrections in his Birds of the Japanese Empire 1890. Accidental stragglers are not reckoned as British birds.
[147] Mr. Swinhoe died in October, 1877, at the early age of forty-two. His writings on natural history are chiefly scattered through the volumes of the Proceedings of the Zoological Society and The Ibis; the whole being summarised in his Catalogue of the Mammals of South China and Formosa (P. Z. S., 1870, p. 615), and his Catalogue of the Birds of China and its Islands (P. Z. S., 1871, p. 337).
[148] Captain Blakiston has shown that the northern island—Yezo—is much more temperate and less peculiar in its zoology than the central and southern islands. This is no doubt dependent chiefly on the considerable change of climate that occurs on passing the Tsu-garu strait.
[149] See Dr. J. E. Gray's "Revision of the Viverridæ," in Proc. Zool. Soc. 1864, p. 507.
[150] Some of the Bats of Madagascar and East Africa are said to have their nearest allies in Australia. (See Dobson in Nature, Vol. XXX. p. 575.)
[151] This view was, I believe, first advanced by Professor Huxley in his "Anniversary Address to the Geological Society," in 1870. He says:—"In fact the Miocene mammalian fauna of Europe and the Himalayan regions contain, associated together, the types which are at present separately located in the South African and Indian provinces of Arctogæa. Now there is every reason to believe, on other grounds, that both Hindostan south of the Ganges, and Africa south of the Sahara, were separated by a wide sea from Europe and North Asia during the Middle and Upper Eocene epochs. Hence it becomes highly probable that the well-known similarities, and no less remarkable differences, between the present faunæ of India and South Africa have arisen in some such fashion as the following: Some time during the Miocene epoch, the bottom of the nummulitic sea was upheaved and converted into dry land in the direction of a line extending from Abyssinia to the mouth of the Ganges. By this means the Dekkan on the one hand and South Africa on the other, became connected with the Miocene dry land and with one another. The Miocene mammals spread gradually over this intermediate dry land; and if the condition of its eastern and western ends offered as wide contrasts as the valleys of the Ganges and Arabia do now, many forms which made their way into Africa must have been different from those which reached the Dekkan, while others might pass into both these sub-provinces."
This question is fully discussed in my Geographical Distribution of Animals (Vol. I., p. 285), where I expressed views somewhat different from those of Professor Huxley, and made some slight errors which are corrected in the present work. As I did not then refer to Professor Huxley's prior statement of the theory of Miocene immigration into Africa (which I had read but the reference to which I could not recall) I am happy to give his views here.
[152] The total number of Madagascar birds is 238, of which 129 are absolutely peculiar to the island, as are thirty-five of the genera. All the peculiar birds but two are land birds. These are the numbers given in M. Grandidier's great work on Madagascar.
[153] The Ibis, 1877, p. 334.
[154] In a paper read before the Geological Society in 1874, Mr. H. F. Blanford, from the similarity of the fossil plants and reptiles, supposed that India and South Africa had been connected by a continent, "and remained so connected with some short intervals from the Permian up to the end of the Miocene period," and Mr. Woodward expressed his satisfaction with "this further evidence derived from the fossil flora of the Mesozoic series of India in corroboration of the former existence of an old submerged continent—Lemuria."
Those who have read the preceding chapters of the present work will not need to have pointed out to them how utterly inconclusive is the fragmentary evidence derived from such remote periods (even if there were no evidence on the other side) as indicating geographical changes. The notion that a similarity in the productions of widely separated continents at any past epoch is only to be explained by the existence of a direct land-connection, is entirely opposed to all that we know of the wide and varying distribution of all types at different periods, as well as to the great powers of dispersal over moderate widths of ocean possessed by all animals except mammalia. It is no less opposed to what is now known of the general permanency of the great continental and oceanic areas; while in this particular case it is totally inconsistent (as has been shown above) with the actual facts of the distribution of animals.
[155] Geographical Distribution of Animals, Vol. I., pp. 272-292.
[156] The term "Mascarene" is used here in an extended sense, to include all the islands near Madagascar which resemble it in their animal and vegetable productions.
[157] For the birds of the Comoro Islands see Proc. Zool. Soc., 1877, p. 295, and 1879, p. 673.
[158] The following is a list of these peculiar birds. (See the Ibis, for 1867, p. 359; and 1879, p. 97.)
Passeres. Ellisia seychelensis. Copsychus seychellarum. Hypsipetes crassirostris. Tchitrea corvina. Nectarinia dussumieri. Zosterops modesta. " semiflava. Foudia seychellarum. Psittaci. Coracopsis barklyi. Palæornis wardi. Columbæ. Alectorænas pulcherrimus. Turtur rostratus. Accipitres. Tinnunculus gracilis.
[159] Specimens are recorded from West Africa in the Proceedings of the Academy of Natural Science, Philadelphia, 1857, p. 72, while specimens in the Paris Museum were brought by D'Orbigny from S. America. Dr. Wright's specimens from the Seychelles have, as he informs me, been determined to be the same species by Dr. Peters of Berlin.
[160] "Additional Notes on the Land-shells of the Seychelles Islands." By Geoffrey Nevill, C.M.Z.S. Proc. Zool. Soc. 1869, p. 61.
[161] In Maillard's Notes sur l'Isle de Réunion, a considerable number of mammalia are given as "wild," such as Lemur mongoz and Centetes setosus, both Madagascar species, with such undoubtedly introduced animals as a wild cat, a hare, and several rats and mice. He also gives two species of frogs, seven lizards, and two snakes. The latter are both Indian species and certainly imported, as are most probably the frogs. Legouat, who resided some years in the island nearly two centuries ago, and who was a closer observer of nature, mentions numerous birds, large bats, land-tortoises, and lizards, but no other reptiles or venomous animals except scorpions. We may be pretty sure, therefore, that the land-mammalia, snakes, and frogs, now found wild, have all been introduced. Of lizards, on the other hand, there are several species, some peculiar to the island, others common to Africa and the other Mascarene Islands. The following list by Prof. Dumeril is given in Maillard's work:—
Platydactylus cepedianus. " ocellatus. Hemidactylus peronii. " mutilatus. Hemidactylus frenatus. Gongylus bojerii. Ablepharus peronii.
Four species of chameleon are now recorded from Bourbon and one from Mauritius (J. Reay Greene, M.D., in Pop. Science Rev. April, 1880), but as they are not mentioned by the old writers, it is pretty certain that these creatures are recent introductions, and this is the more probable as they are favourite domestic pets.
Darwin informed me that in a work entitled Voyage à l'Isle de France, par un Officier du Roi, published in 1770, it is stated that a fresh-water fish had been introduced from Batavia and had multiplied. The writer also says (p. 170): "On a essayé, mais sans succcès, d'y transporter des grenouilles qui mangent les œufs que les moustigues deposent sur les eaux stagnantes." It thus appears that there were then no frogs on the island.
[162] That the dodo is really an abortion from a more perfect type, and not a direct development from some lower form of wingless bird, is shown by its possessing a keeled sternum, though the keel is exceedingly reduced, being only three-quarters of an inch deep in a length of seven inches. The most terrestrial pigeon—the Didunculus of the Samoan Islands, has a far deeper and better developed keel, showing that in the case of the dodo the degradation has been extreme. We have also analogous examples in other extinct birds of the same group of islands, such as the flightless Rails—Aphanapteryx of Mauritius and Erythromachus of Rodriguez, as well as the large parrot—Lophopsittacus of Mauritius, and the Night Heron, Nycticorax megacephala of Rodriguez, the last two birds probably having been able to fly a little. The commencement of the same process is to be seen in the peculiar dove of the Seychelles, Turtur rostratus, which, as Mr. Edward Newton has shown, has much shorter wings than its close ally, T. picturatus, of Madagascar. For a full and interesting account of these and other recently extinct birds see Professor Newton's article on "Fossil Birds" in the Encyclopædia Britannica, ninth edition, vol. iii., p. 732; and that on "The Extinct Birds of Rodriguez," by Dr. A. Günther and Mr. E. Newton, in the Royal Society's volume on the Transit of Venus Expedition.
[163] See Ibis, 1877, p. 334.
[164] A common Indian and Malayan toad (Bufo melanostictus) has been introduced into Mauritius and also some European toads, as I am informed by Dr. Günther.
[165] This brief account of the Madagascar flora has been taken from a very interesting paper by the Rev. Richard Baron, F.L.S., F.G.S., in the Journal of the Linnean Society, Vol. XXV., p. 246; where much information is given on the distribution of the flora within the island.
[166] It may be interesting to botanists and to students of geographical distribution to give here an enumeration of the endemic genera of the Flora of the Mauritius and the Seychelles, as they are nowhere separately tabulated in that work.
Aphloia (Bixaceæ) 1 sp., a shrub, Maur., Rod., Sey., also Madagascar.
Medusagyne (Ternströmiaceæ) 1 sp., a shrub, Seychelles.
Astiria (Sterculiaceæ) 1 sp., a shrub, Mauritius.
Quivisia (Meliaceæ) 3 sp., shrubs, Mauritius (2 sp.), Rodriguez (1 sp.), also Bourbon.
Cossignya (Sapindaceæ) 1 sp., a shrub, Mauritius, also Bourbon.
Hornea ,, 1 sp., a shrub, Mauritius.
Stadtmannia ,, 1 sp., a shrub, Mauritius.
Doratoxylon ,, 1 sp., a shrub, Mauritius and Bourbon.
Gagnebina (Leguminosæ) 1 sp., a shrub, Mauritius, also Madagascar.
Roussea (Saxifragaceæ) 1 sp., a climbing shrub, Mauritius and Bourbon.
Tetrataxis (Lythraceæ) 1 sp., a shrub, Mauritius.
Psiloxylon ,, 1 sp., a shrub, Mauritius and Bourbon.
Mathurina (Turneraceæ) 1 sp., a shrub, Rodriguez.
Fœtidia (Myrtaceæ) 1 sp., a tree, Mauritius.
Danais (Rubiaceæ) 4 sp., climbing shrubs, Maur. (1 sp.), Rodr. (1 sp.), also Bourbon and Madagascar.
Fernelia (Rubiaceæ) 1 sp., a shrub, Mauritius and Rodriguez.
Pyrostria ,, 6 sp., shrubs, Mauritius (3 sp.), also Bourbon and Madagascar.
Scyphochlamys (Rubiaceæ) 1 sp., a shrub, Rodriguez.
Myonima ,, 3 sp., shrubs, Mauritius, also Bourbon.
Cylindrocline (Compositæ) 1 sp., a shrub, Mauritius.
Monarrhenus ,, 2 sp., shrubs, Mauritius, also Bourbon and Madagascar.
Faujasia (Compositæ) 3 sp., shrubs, Mauritius, also Bourbon and Madagascar.
Heterochænia (Campanulaceæ) 1 sp., a shrub, Mauritius, also Bourbon.
Tanulepis (Asclepiadaceæ) 1 sp., a climber, Rodriguez.
Decanema ,, 1 sp., a climber, Mauritius, also Madagascar.
Nicodemia (Loganiaceæ) 2 sp., shrubs, Mauritius (1 sp.), also Comoro Islands and Madagascar.
Bryodes (Scrophulariaceæ) 1 sp., herb, Mauritius.
Radamæa ,, 2 sp., herb, Seychelles (1 sp.), and Madagascar.
Colea (Bignoniaceæ) 10 sp., Mauritius (1 sp.), Seychelles (1 sp.), also Bourbon and Madagascar. (Shrubs, trees, or climbers.)
Obetia (Urticaceæ) 2 sp., shrubs, Mauritius, Seychelles, and Madagascar.
Bosquiea (Moreæ) 3 sp., trees, Seychelles (1 sp.), also Madagascar.
Monimia (Monimiaceæ) 3 sp., trees, Mauritius (2 sp.), also Bourbon.
Cynorchis (Orchideæ) 3 sp., herb, ter., Mauritius.
Amphorchis ,, 1 sp., herb, ter., Mauritius, also Bourbon.
Arnottia ,, 2 sp., herb, ter., Mauritius, also Bourbon.
Aplostellis ,, 1 sp., herb, ter., Mauritius.
Cryptopus ,, 1 sp., herb, Epiphyte, Mauritius, also Bourbon and Madagascar.
Lomatophyllum (Liliaceæ) 3 sp., shrubs (succulent), Mauritius, also Bourbon.
Lodoicea (Palmæ) 1 sp., tree, Seychelles.
Latania ,, 3 sp., trees, Mauritius (2 sp.), Rodriguez, also Bourbon.
Hyophorbe ,, 3 sp., trees, Mauritius (2 sp.), Rodriguez, also Bourbon.
Dictyosperma ,, 1 sp., tree, Mauritius, Rodriguez, also Bourbon.
Acanthophænix ,, 2 sp., trees, Mauritius, also Bourbon.
Deckenia ,, 1 sp., tree, Seychelles.
Nephrosperma ,, 1 sp., tree, Seychelles.
Roscheria ,, 1 sp., tree, Seychelles.
Verschaffeltia ,, 1 sp., tree, Seychelles.
Stevensonia ,, 1 sp., tree, Seychelles.
Ochropteris (Filices) 1 sp., herb, Mauritius, also Bourbon and Madagascar.
Among the curious features in this list are the great number of endemic shrubs in Mauritius, and the remarkable assemblage of five endemic genera of palms in the Seychelles Islands. We may also notice that one palm (Latania loddigesii) is confined to Round Island and two other adjacent islets offering a singular analogy to the peculiar snake also found there.
[167]
Families of Malayan Birds not found in islands East of Celebes. Families of Moluccan Birds not found in islands West of Celebes.
Troglodytidæ. Sittidæ. Paridæ. Liotrichidæ. Phyllornithidæ. Eurylæmidæ. Picidæ. Indicatoridæ. Megalænidæ. Trogonidæ. Phasianidæ. Paradiseidæ. Meliphagidæ. Cacatuidæ. Platycercidæ. Trichoglossidæ. Nestoridæ.
[168] For outline figures of the chief types of these butterflies, see my Malay Archipelago, Vol. I. p. 441, or p. 216 of the tenth edition.
[169] Dobson on the Classification of Chiroptera (Ann. and Mag. of Nat. Hist. Nov. 1875).
[170] See Buller, "On the New Zealand Rat," Trans. of the N. Z. Institute (1870), Vol. III. p. 1, and Vol. IX. p. 348; and Hutton, "On the Geographical Relations of the New Zealand Fauna," Trans. N. Z. Instit. 1872, p. 229.
[171] Hochstetter's New Zealand, p. 161, note.
[172] The animal described by Captain Cook as having been seen at Pickersgill Harbour in Dusky Bay (Cook's 2nd Voyage, Vol. I. p. 98) may have been the same creature. He says, "A four-footed animal was seen by three or four of our people, but as no two gave the same description of it, I cannot say what kind it is. All, however, agreed that it was about the size of a cat, with short legs, and of a mouse colour. One of the seamen, and he who had the best view of it, said it had a bushy tail, and was the most like a jackal of any animal he knew." It is suggestive that, so far as the points on which "all agreed"—the size and the dark colour—this description would answer well to the animal so recently seen, while the "short legs" correspond to the otter-like tracks, and the thick tail of an otter-like animal may well have appeared "bushy" when the fur was dry. It has been suggested that it was only one of the native dogs; but as none of those who saw it took it for a dog, and the points on which they all agreed are not dog-like, we can hardly accept this explanation; while the actual existence of an unknown animal in New Zealand of corresponding size and colour is confirmed by this account of a similar animal having been seen about a century ago.
[173] Owen, "On the Genus Dinornis," Trans. Zool. Soc. Vol. X. p. 184. Mivart, "On the Axial Skeleton of the Struthionidæ," Trans. Zool. Soc. Vol. X. p. 51.
[174] The recent existence of the Moa and its having been exterminated by the Maoris appears to be at length set at rest by the statement of Mr. John White, a gentleman who has been collecting materials for a history of the natives for thirty-five years, who has been initiated by their priests into all their mysteries, and is said to "know more about the history, habits, and customs of the Maoris than they do themselves." His information on this subject was obtained from old natives long before the controversy on the subject arose. He says that the histories and songs of the Maoris abound in allusions to the Moa, and that they were able to give full accounts of "its habits, food, the season of the year it was killed, its appearance, strength, and all the numerous ceremonies which were enacted by the natives before they began the hunt, the mode of hunting, how cut up, how cooked, and what wood was used in the cooking, with an account of its nest, and how the nest was made, where it usually lived, &c." Two pages are occupied by these details, but they are only given from memory, and Mr. White promises a full account from his MSS. Many of the details given correspond with facts ascertained from the discovery of native cooking places with Moas' bones; and it seems quite incredible that such an elaborate and detailed account should be all invention. (See Transactions of the New Zealand Institute, Vol. VIII. p. 79.)
[175] See fig. in Trans. of N. Z. Institute, Vol. III., plate 12b. fig. 2.
[176] Geographical Distribution of Animals, Vol. I., p. 450.
[177] In my Geographical Distribution of Animals (I. p. 541) I have given two peculiar Australian genera (Orthonyx and Tribonyx) as occurring in New Zealand. But the former has been found in New Guinea, while the New Zealand bird is considered to form a distinct genus, Clitonyx; and the latter inhabits Tasmania, and was recorded from New Zealand through an error. (See Ibis, 1873, p. 427.)
[178] The peculiar genera of Australian lizards according to Boulenger's British Museum Catalogue, are as follows:—Family Geckonidæ: Nephrurus, Rhynchœdura, Heteronota, Diplodactylus, Œdura. Family Pygopodidæ (peculiar): Pygopus, Cryptodelma, Delma, Pletholax, Aprasia. Family Agamidæ: Chelosania, Amphibolurus, Tympanocryptis, Diporophora, Chlamydosaurus, Moloch, Oreodeira. Family Scincidæ: Egerina, Trachysaurus, Hemisphænodon. Family doubtful: Ophiopsiseps.
[179] These figures are taken from Mr. G. M. Thomson's address "On the Origin of the New Zealand Flora," Trans. N. Z. Institute, XIV. (1881), being the latest that I can obtain. They differ somewhat from those given in the first edition, but not so as to affect the conclusions drawn from them.
[180] This accords with the general scarcity of Leguminosæ in Oceanic Islands, due probably to their usually dry and heavy seeds, not adapted to any of the forms of aërial transmission; and it would indicate either that New Zealand was never absolutely united with Australia, or that the union was at a very remote period when Leguminosæ were either not differentiated or comparatively rare.
[181] Sir Joseph Hooker informs me that the number of tropical Australian plants discovered within the last twenty years is very great, and that the statement as above made may have to be modified. Looking, however, at the enormous disproportion of the figures given in the "Introductory Essay" in 1859 (2,200 tropical to 5,800 temperate species) it seems hardly possible that a great difference should not still exist, at all events as regards species. In Baron von Müeller's latest summary of the Australian Flora (Second Systematic Census of Australian Plants, 1889), he gives the total species at 8,839, of which 3,560 occur in West Australia, and 3,251 in New South Wales. On counting the species common to these two colonies in fifty pages of the Census taken at random, I find them to be about one-tenth of the total species in both. This would give the number of distinct species in these areas as about 6,130. Adding to these the species peculiar to Victoria and South Australia, we shall have a flora of near 6,500 in the temperate parts of Australia. It is true that West Australia extends far into the tropics, but an overwhelming majority of the species have been discovered in the south-western portion of the colony, while the species that may be exclusively tropical will be more than balanced by those of temperate Queensland, which have not been taken account of, as that colony is half temperate and half tropical. It thus appears probable that full three fourths of the species of Australian plants occur in the temperate regions, and are mainly characteristic of it. Sir Joseph Hooker also doubts the generally greater richness of tropical over temperate floras which I have taken as almost an axiom. He says: "Taking similar areas to Australia in the Western World, e.g., tropical Africa north of 20° S. Lat. as against temperate Africa and Europe up to 47°—I suspect that the latter would present more genera and species than the former." This, however, appears to me to be hardly a case in point, because Europe is a distinct continent from Africa and has had a very different past history, and it is not a fair comparison to take the tropical area in one continent while the temperate is made up of widely separated areas in two continents. A closer parallel may perhaps be found in equal areas of Brazil and south temperate America, or of Mexico and the Southern United States, in both of which cases I suppose there can be little doubt that the tropical areas are far the richest. Temperate South Africa is, no doubt, always quoted as richer than an equal area of tropical Africa or perhaps than any part of the world of equal extent, but this is admitted to be an exceptional case.
[182] Sir Joseph Hooker thinks that later discoveries in the Australian Alps and other parts of East and South Australia may have greatly modified or perhaps reversed the above estimate, and the figures given in the preceding note indicate that this is so. But still, the small area of South-west Australia will be, proportionally, far the richer of the two. It is much to be desired that the enormous mass of facts contained in Mr. Bentham's Flora Australiensis and Baron von Müeller's Census should be tabulated and compared by some competent botanist, so as to exhibit the various relations of its wonderful vegetation in the same manner as was done by Sir Joseph Hooker with the materials available twenty-one years ago.
[183] From an examination of the fossil corals of the South-west of Victoria, Professor P. M. Duncan concludes—"that, at the time of the formation of these deposits the central area of Australia was occupied by sea, having open water to the north, with reefs in the neighbourhood of Java." The age of these fossils is not known, but as almost all are extinct species, and some are almost identical with European Pliocene and Miocene species, they are supposed to belong to a corresponding period. (Journal of Geol. Soc., 1870.)
[184] "On the Origin of the Fauna and Flora of New Zealand," by Captain F. W. Hutton, in Annals and Mag. of Nat. Hist. Fifth series, p. 427 (June, 1884).
[185] To these must now be added the genera Sequoia, Myrica, Aralia, and Acer, described by Baron von Ettingshausen. (Trans. N.Z. Institute, xix., p. 449.)
[186] The large collection of fossil plants from the Tertiary beds of New Zealand which have been recently described by Baron von Ettingshausen (Trans. N. Z. Inst., vol. xxiii., pp. 237-310), prove that a change in the vegetation has occurred similar to that which has taken place in Eastern Australia, and that the plants of the two countries once resembled each other more than they do now. We have, first, a series of groups now living in Australia, but which have become extinct in New Zealand, as Cassia, Dalbergia, Eucalyptus, Diospyros, Dryandra, Casuarina, and Ficus; and also such northern genera as Acer, Planera, Ulmus, Quercus, Alnus, Myrica, and Sequoia. All these latter, except Ulmus and Planera, have been found also in the Eastern-Australian Tertiaries, and we may therefore consider that at this period the northern temperate element in both floras was identical. If this flora entered both countries from the south, and was really Antarctic, its extinction in New Zealand may have been due to the submergence of the country to the south, and its elevation and extension towards the tropics, admitting of the incursion of the large number of Polynesian and tropical Australian types now found there; while the Australian portion of the same flora may have succumbed at a somewhat later period, when the elevation of the Cretaceous and Tertiary sea united it with Western Australia, and allowed the rich typical Australian flora to overrun the country. Of course we are assuming that the identification of these genera is for the most part correct, though almost entirely founded on leaves only. Fuller knowledge, both of the extinct flora itself and of the geological age of the several deposits, is requisite before any trustworthy explanation of the phenomena can be arrived at.
[187] The following are the tropical genera common to New Zealand and Australia:—
1. Melicope. Queensland, Pacific Islands. 2. Eugenia. Eastern and Tropical Australia, Asia, and America. 3. Passiflora. N.S.W. and Queensland, Tropics of Old World and America. 4. Myrsine. Tropical and Temperate Australia, Tropical and Sub-tropical regions. 5. Sapota. Australia, Norfolk Islands, Tropics. 6. Cyathodes. Australia and Pacific Islands. 7. Parsonsia. Tropical Australia and Asia. 8. Geniostoma. Queensland, Polynesia, Asia. 9. Mitrasacme. Tropical and Temperate Australia, India. 10. Ipomœa. Tropical Australia, Tropics. 11. Mazus. Temperate Australia, India, China. 12. Vitex. Tropical Australia, Tropical and Sub-tropical. 13. Pisonia. Tropical Australia, Tropical and Sub-tropical. 14. Alternanthera. Tropical Australia, India, and S. America. 15. Tetranthera. Tropical Australia, Tropics. 16. Santalum. Tropical and Sub-tropical Australia, Pacific, Malay Islands. 17. Carumbium. Tropical and Sub-tropical Australia, Pacific Islands. 18. Elatostemma. Sub-tropical Australia, Asia, Pacific Islands. 19. Peperomia. Tropical and Sub-tropical Australia, Tropics. 20. Piper. Tropical and Sub-tropical Australia, Tropics. 21. Dacrydium. Tasmania, Malay, and Pacific Islands. 22. Dammara. Tropical Australia, Malay, and Pacific Islands. 23. Dendrobium. Tropical Australia, Eastern Tropics. 24. Bolbophyllum. Tropical and Sub-tropical Australia, Tropics. 25. Sarcochilus. Tropical and Sub-tropical Australia, Fiji, and Malay Islands. 26. Freycinetia. Tropical Australia, Tropical Asia. 27. Cordyline. Tropical Australia, Pacific Islands. 28. Dianella. Australia, India, Madagascar, Pacific Islands. 29. Cyperus. Australia, Tropical regions mainly. 30. Fimbristylis. Tropical Australia, Tropical regions. 31. Paspalum. Tropical and Sub-tropical grasses. 32. Isachne. Tropical and Sub-tropical grasses. 33. Sporobolus. Tropical and Sub-tropical grasses.
[188] Insects are tolerably abundant in the open mountain regions, but very scarce in the forests. Mr. Meyrick says that these are "strangely deficient in insects, the same species occurring throughout the islands;" and Mr. Pascoe remarked that "the forests of New Zealand were the most barren country, entomologically, he had ever visited." (Proc. Ent. Soc., 1883. p. xxix.)
[189] Introductory Essay On the Flora of Australia, p. 130.
[190] Hooker, On the Flora of Australia, p. 95.—H. C. Watson, in Godman's Azores, pp. 278-286.
[191] As this is a point of great interest in its bearing on the dispersal of plants by means of mountain ranges, I have endeavoured to obtain a few illustrative facts:—
1. Mr. William Mitten, of Hurstpierpoint, Sussex, informs me that when the London and Brighton railway was in progress in his neighbourhood, Melilotus vulgaris made its appearance on the banks, remained for several years, and then altogether disappeared. Another case is that of Diplotaxis muralis, which formerly occurred only near the sea-coast of Sussex, and at Lewes; but since the railway was made has spread along it, and still maintains itself abundantly on the railway banks though rarely found anywhere else.
2. A correspondent in Tasmania informs me that whenever the virgin forest is cleared in that island there invariably comes up a thick crop of a plant locally known as fire-weed—a species of Senecio, probably S. Australis. It never grows except where the fire has gone over the ground, and is unknown except in such places. My correspondent adds:—"This autumn I went back about thirty-five miles through a dense forest, along a track marked by some prospectors the year before, and in one spot where they had camped, and the fire had burnt the fallen logs, &c., there was a fine crop of 'fire-weed.' All around for many miles was a forest of the largest trees and dense scrub." Here we have a case in which burnt soil and ashes favour the germination of a particular plant, whose seeds are easily carried by the wind, and it is not difficult to see how this peculiarity might favour the dispersal of the species for enormous distances, by enabling it temporarily to grow and produce seeds on burnt spots.
3. In answer to an inquiry on this subject, Mr. H. C. Watson has been kind enough to send me a detailed account of the progress of vegetation on the railway banks and cuttings about Thames Ditton. This account is written from memory, but as Mr. Watson states that he took a great interest in watching the process year by year, there can be no reason to doubt the accuracy of his memory. I give a few extracts which bear especially on the subject we are discussing.
"One rather remarkable biennial plant appeared early (the second year, as I recollect) and renewed itself either two or three years, namely, Isatis tinctoria—a species usually supposed, to be one of our introduced, but pretty well naturalised, plants. The nearest stations then or since known to me for this Isatis are on chalk about Guildford, twenty miles distant. There were two or three plants of it at first, never more than half a dozen. Once since I saw a plant of Isatis on the railway bank near Vauxhall.
"Close by Ditton Station three species appeared which may be called interlopers. The biennial Barbarea precox, one of these, is the least remarkable, because it might have come as seed in the earth from some garden, or possibly in the Thames gravel (used as ballast). At first it increased to several plants, then became less numerous, and will soon, in all probability, become extinct, crowded out by other plants. The biennial Petroselinum segetum was at first one very luxuriant plant on the slope of the embankment. It increased by seed into a dozen or a score, and is now nearly if not quite extinct. The third species is Linaria purpurea, not strictly a British plant, but one established in some places on old walls. A single root of it appeared on the chalk facing of the embankment by Ditton Station. It has remained there several years and grown into a vigorous specimen. Two or three smaller examples are now seen by it, doubtless sprung from some of the hundreds or thousands of seeds shed by the original one plant. The species is not included in Salmon and Brewer's Flora of Surrey.
"The main line of the railway has introduced into Ditton parish the perennial Arabis hirsuta, likely to become a permanent inhabitant. The species is found on the chalk and greensand miles away from Thames Ditton; but neither in this parish nor in any adjacent parish, so far as known to myself or to the authors of the flora of the county, does it occur. Some years after the railway was made a single root of this Arabis was observed in the brickwork of an arch by which the railway is carried over a public road. A year or two afterwards there were three or four plants. In some later year I laid some of the ripened seed-pods between the bricks in places where the mortar had partly crumbled out. Now there are several scores of specimens in the brickwork of the arch. It is presumable that the first seed may have been brought from Guildford. But how could it get on to the perpendicular face of the brickwork?
"The Bee Orchis (Ophrys apifera), plentiful on some of the chalk lands in Surrey, is not a species of Thames Ditton, or (as I presume) of any adjacent parish. Thus, I was greatly surprised some years back to see about a hundred examples of it in flower in one clayey field either on the outskirts of Thames Ditton or just within the limits of the adjoining parish of Cobham. I had crossed this same field in a former year without observing the Ophrys there. And on finding it in the one field I closely searched the surrounding fields and copses, without finding it anywhere else. Gradually the plants became fewer and fewer in that one field, and some six or eight years after its first discovery there the species had quite disappeared again. I guessed it had been introduced with chalk, but could obtain no evidence to show this."
4. Mr. A. Bennett, of Croydon, has kindly furnished me with some information on the temporary vegetation of the banks and cuttings on the railway from Yarmouth to Caistor in Norfolk, where it passes over extensive sandy Denes with a sparse vegetation. The first year after the railway was made the banks produced abundance of Œnothera odorata and Delphinium Ajacis (the latter only known thirty miles off in cornfields in Cambridgeshire), with Atriplex patula and A. deltoidea. Gradually the native sand plants—Carices, Grasses, Galium verum, &c., established themselves, and year by year covered more ground till the new introductions almost completely disappeared. The same phenomenon was observed in Cambridgeshire between Chesterton and Newmarket, where, the soil being different, Stellaria media and other annuals appeared in large patches; but these soon gave way to a permanent vegetation of grasses, composites, &c., so that in the third year no Stellaria was to be seen.
5. Mr. T. Kirk (writing in 1878) states that—"in Auckland, where a dense sward of grass is soon formed, single specimens of the European milk Thistle (Carduus marianus) have been known for the past fifteen years; but although they seeded freely, the seeds had no opportunity of germinating, so that the thistle did not spread. A remarkable exception to this rule occurred during the formation of the Onehunga railway, where a few seeds fell on disturbed soil, grew up and flowered. The railway works being suspended, the plant increased rapidly, and spread wherever it could find disturbed soil."
Again:—"The fiddle-dock (Rumex pulcher) occurs in great abundance on the formation of new streets, &c., but soon becomes comparatively rare. It seems probable that it was one of the earliest plants naturalised here, but that it partially died out, its buried seeds retaining their vitality."
Medicago sativa and Apium graveolens, are also noted as escapes from cultivation which maintain themselves for a time but soon die out. (Transactions of the New Zealand Institute, Vol. X. p. 367.)
The preceding examples of the temporary establishment of plants on newly exposed soil, often at considerable distances from the localities they usually inhabit, might, no doubt, by further inquiry be greatly multiplied; but, unfortunately, the phenomenon has received little attention, and is not even referred to in the elaborate work of De Candolle (Géographie Botanique Raisonnée) in which almost every other aspect of the dispersion and distribution of plants is fully discussed. Enough has been advanced, however, to show that it is of constant occurrence, and from the point of view here advocated it becomes of great importance in explaining the almost world-wide distribution of many common plants of the north temperate zone.
[192] Sir Joseph Hooker informs me that he considers these identifications worthless, and Mr. Bentham has also written very strongly against the value of similar identifications by Heer and Unger. Giving due weight to the opinions of these eminent botanists we must admit that Australian genera have not yet been demonstrated to have existed in Europe during the Tertiary period; but, on the other hand, the evidence that they did so appears to have some weight, on account of the improbability that the numerous resemblances to Australian plants which have been noticed by different observers should all be illusory; while the well established fact of the former wide distribution of many tropical or now restricted types of plants and animals, so frequently illustrated in the present volume, removes the antecedent improbability which is supposed to attach to such identifications. I am myself the more inclined to accept them, because, according to the views here advocated, such migrations must have taken place at remote as well as at recent epochs; and the preservation of some of these types in Australia while they have become extinct in Europe, is exactly paralleled by numerous facts in the distribution of animals which have been already referred to in Chapter XIX., and elsewhere in this volume, and also repeatedly in my larger work.
[193] Out of forty-two genera from the Eocene of Sheppey enumerated by Dr. Ettingshausen in the Geological Magazine for January 1880, only two or three appear to be extinct, while there is a most extraordinary intermixture of tropical and temperate forms—Musa, Nipa, and Victoria, with Corylus, Prunus, Acer, &c. The rich Miocene flora of Switzerland, described by Professor Heer, presents a still larger proportion of living genera.
[194] The recent discovery by Lieutenant Jensen of a rich flora on rocky peaks rising out of the continental ice of Greenland, as well as the abundant vegetation of the highest northern latitudes, renders it possible that even now the Antarctic continent may not be wholly destitute of vegetation, although its climate and physical condition are far less favourable than those of the Arctic lands. (See Nature, Vol. XXI. p. 345.)
[195] Dr. Hector notes the occurrence of the genus Dammara in Triassic deposits, while in the Jurassic period New Zealand possessed the genera Palæozamia, Oleandrium, Alethopteris, Camptopteris, Cycadites, Echinostrobus, &c., all Indian forms of the same age. Neocomian beds contain a true dicotyledonous leaf with Dammara and Araucaria. The Cretaceous deposits have produced a rich flora of dicotyledonous plants, many of which are of the same genera as the existing flora; while the Miocene and other Tertiary deposits produce plants almost identical with those now inhabiting the country, together with many North Temperate genera which have since become extinct. (See p. 499, footnote, and Trans. New Zealand Inst., Vol. XI. 1879, p. 536.)
[196] The fact stated in the last edition of the Origin of Species (p. 340) on the authority of Sir Joseph Hooker, that Australian plants are rapidly sowing themselves and becoming naturalised on the Neilgherrie mountains in the southern part of the Indian Peninsula, though an exception to the rule of the inability of Australian plants to become naturalised in the Northern Hemisphere, is yet quite in harmony with the hypothesis here advocated. For not only is the climate of the Neilgherries more favourable to Australian plants than any part of the North Temperate zone, but the entire Indian Peninsula has existed for unknown ages as an island and thus possesses the "insular" characteristic of a comparatively poor and less developed flora and fauna as compared with the truly "continental" Malayan and Himalayan regions. Australian plants are thus enabled to compete with those of the Indian Peninsula highlands with a fair chance of success.