Glancing at instincts, marvellous as some are, they offer no greater difficulty than do corporeal structures on the theory of the natural selection of successive, slight, but profitable modifications. We can thus understand why nature moves by graduated steps in endowing different animals of the same class with their several instincts. I have attempted to show how much light the principle of gradation throws on the admirable architectural powers of the hive-bee. Habit no doubt often comes into play in modifying instincts; but it certainly is not indispensable, as we see in the case of neuter insects, which leave no progeny to inherit the effects of long-continued habit. On the view of all the species of the same genus having descended from a common parent, and having inherited much in common, we can understand how it is that allied species, when placed under widely different conditions of life, yet follow nearly the same instincts; why the thrushes of tropical and temperate South America, for instance, line their nests with mud like our British species. On the view of instincts having been slowly acquired through natural selection, we need not marvel at some instincts being not perfect and liable to mistakes, and at many instincts causing other animals to suffer.

If species be only well-marked and permanent varieties, we can at once see why their crossed offspring should follow the same complex laws in their degrees and kinds of resemblance to their parents--in being absorbed into each other by successive crosses, and in other such points--as do the crossed offspring of acknowledged varieties. This similarity would be a strange fact, if species had been independently created and varieties had been produced through secondary laws.

If we admit that the geological record is imperfect to an extreme degree, then the facts, which the record does give, strongly support the theory of descent with modification. New species have come on the stage slowly and at successive intervals; and the amount of change after equal intervals of time, is widely different in different groups. The extinction of species and of whole groups of species, which has played so conspicuous a part in the history of the organic world, almost inevitably follows from the principle of natural selection; for old forms are supplanted by new and improved forms. Neither single species nor groups of species reappear when the chain of ordinary generation is once broken. The gradual diffusion of dominant forms, with the slow modification of their descendants, causes the forms of life, after long intervals of time, to appear as if they had changed simultaneously throughout the world. The fact of the fossil remains of each formation being in some degree intermediate in character between the fossils in the formations above and below, is simply explained by their intermediate position in the chain of descent. The grand fact that all extinct beings can be classed with all recent beings, naturally follows from the living and the extinct being the offspring of common parents. As species have generally diverged in character during their long course of descent and modification, we can understand why it is that the more ancient forms, or early progenitors of each group, so often occupy a position in some degree intermediate between existing groups. Recent forms are generally looked upon as being, on the whole, higher in the scale of organisation than ancient forms; and they must be higher, in so far as the later and more improved forms have conquered the older and less improved forms in the struggle for life; they have also generally had their organs more specialised for different functions. This fact is perfectly compatible with numerous beings still retaining simple and but little improved structures, fitted for simple conditions of life; it is likewise compatible with some forms having retrograded in organisation, by having become at each stage of descent better fitted for new and degraded habits of life. Lastly, the wonderful law of the long endurance of allied forms on the same continent--of marsupials in Australia, of edentata in America, and other such cases--is intelligible, for within the same country the existing and the extinct will be closely allied by descent.

Looking to geographical distribution, if we admit that there has been during the long course of ages much migration from one part of the world to another, owing to former climatical and geographical changes and to the many occasional and unknown means of dispersal, then we can understand, on the theory of descent with modification, most of the great leading facts in Distribution. We can see why there should be so striking a parallelism in the distribution of organic beings throughout space, and in their geological succession throughout time; for in both cases the beings have been connected by the bond of ordinary generation, and the means of modification have been the same. We see the full meaning of the wonderful fact, which has struck every traveller, namely, that on the same continent, under the most diverse conditions, under heat and cold, on mountain and lowland, on deserts and marshes, most of the inhabitants within each great class are plainly related; for they are the descendants of the same progenitors and early colonists. On this same principle of former migration, combined in most cases with modification, we can understand, by the aid of the Glacial period, the identity of some few plants, and the close alliance of many others, on the most distant mountains, and in the northern and southern temperate zones; and likewise the close alliance of some of the inhabitants of the sea in the northern and southern temperate latitudes, though separated by the whole intertropical ocean. Although two countries may present physical conditions as closely similar as the same species ever require, we need feel no surprise at their inhabitants being widely different, if they have been for a long period completely sundered from each other; for as the relation of organism to organism is the most important of all relations, and as the two countries will have received colonists at various periods and in different proportions, from some other country or from each other, the course of modification in the two areas will inevitably have been different.

On this view of migration, with subsequent modification, we see why oceanic islands are inhabited by only few species, but of these, why many are peculiar or endemic forms. We clearly see why species belonging to those groups of animals which cannot cross wide spaces of the ocean, as frogs and terrestrial mammals, do not inhabit oceanic islands; and why, on the other hand, new and peculiar species of bats, animals which can traverse the ocean, are often found on islands far distant from any continent. Such cases as the presence of peculiar species of bats on oceanic islands and the absence of all other terrestrial mammals, are facts utterly inexplicable on the theory of independent acts of creation.

The existence of closely allied representative species in any two areas, implies, on the theory of descent with modification, that the same parent- forms formerly inhabited both areas; and we almost invariably find that wherever many closely allied species inhabit two areas, some identical species are still common to both. Wherever many closely allied yet distinct species occur, doubtful forms and varieties belonging to the same groups likewise occur. It is a rule of high generality that the inhabitants of each area are related to the inhabitants of the nearest source whence immigrants might have been derived. We see this in the striking relation of nearly all the plants and animals of the Galapagos Archipelago, of Juan Fernandez, and of the other American islands, to the plants and animals of the neighbouring American mainland; and of those of the Cape de Verde Archipelago, and of the other African islands to the African mainland. It must be admitted that these facts receive no explanation on the theory of creation.

The fact, as we have seen, that all past and present organic beings can be arranged within a few great classes, in groups subordinate to groups, and with the extinct groups often falling in between the recent groups, is intelligible on the theory of natural selection with its contingencies of extinction and divergence of character. On these same principles we see how it is that the mutual affinities of the forms within each class are so complex and circuitous. We see why certain characters are far more serviceable than others for classification; why adaptive characters, though of paramount importance to the beings, are of hardly any importance in classification; why characters derived from rudimentary parts, though of no service to the beings, are often of high classificatory value; and why embryological characters are often the most valuable of all. The real affinities of all organic beings, in contradistinction to their adaptive resemblances, are due to inheritance or community of descent. The Natural System is a genealogical arrangement, with the acquired grades of difference, marked by the terms, varieties, species, genera, families, etc.; and we have to discover the lines of descent by the most permanent characters, whatever they may be, and of however slight vital importance.

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