This is a brief review of the facts, more detailed in some cases than in others. It remains to review and compare the results arrived at.
The first general statement that may be made is that this faculty of extending their range beyond the limits assigned by nature is not confined to any one family. For all the chief sub-divisions of the terrestrial Oligochaeta seem to possess it, though in unequal degrees. But the inequality may be more apparent than real. For if it be recollected that the species of the family Megascolecidae are very much more numerous than those of the Eudrilidae or even the Geoscolecidae, the fact that there are more peregrine Megascolecidae will lose some of its importance. With the Lumbricidae the case seems to me to be different. Here the preponderance, not only in species (relatively speaking) but in individuals, is much above that of other families. This preponderance I should be disposed to assign to the newness of the family coupled with the vigour seen in new races. That this is a possible explanation is borne out by the fact that the 'Perichaetidae' (i.e. the genus Pheretima) is the most salient race of peregrine Megascolecidae, and it is now generally held that this group is the most modern of that enormous family.
Another general statement may be made with even more confidence, viz. that it appears to be an undoubted fact that some species are more capable of extending themselves than others. Thus Eudrilus eugeniae occurs everywhere on the great land masses of the globe, except in Europe; it is in fact circummundane in the tropical zone, as is also Pontoscolex. Dichogaster bolavi is again a trifle more restricted in its range, having been recorded from tropical Africa, South America, West Indies, Madagascar, and India. Its occurrence near Hamburg in Europe is also to be noted. A little more restricted still is Nematogenia panamaensis whose range is in Central America, tropical West Africa, and Ceylon. Lastly there are cases such as Pheretima taprobanae which, a native of Ceylon, is also found in Madagascar.
It may be asserted in the third place that there are no peculiarities of structure shared by all of these peregrine forms which might account for their physiological similarity, except indeed the somewhat negative feature which they have in common, that is of being of small or moderate size. Eudrilus and Pontoscolex are not isolated types in their respective families; nor do they seem to approach each other in any respect. Nor can it fairly be said that these peregrine species are marked by any great variability of structure as compared with other forms, which might allow for their suiting themselves to various climates and conditions. It is true that Eudrilus eugeniae has received many names which might at first argue some variability. But these names have been perhaps given by persons rather under the influence of the idea that remote habitat implied specific difference, and who were thus inclined to see minute differences, and who perhaps were furthermore led astray in the matter by imperfectly accurate descriptions on the part of others. Certainly some of the peregrine species of Pheretima are subject to some variation, particularly in the number and arrangement of their genital pupillae. But this feature is by no means confined to those species and cannot be utilised as in any way an adaptation to wide distribution.
But while we can lay down no general explanation of the phenomenon, it is possible to furnish some explanation of particular cases. Thus the genus Microscolex is the only exotic genus which appears to have established itself in Europe, from which country indeed it was early known as an apparently indigenous inhabitant. We must put this and some similar cases down to ability to do without great heat. It is probable in fact that the original home of Microscolex is the antarctic half of the globe; and this of itself would allow of its establishing a new home in the northern hemisphere, did other circumstances allow of it.
It might be urged that this genus has been able to establish itself in Europe because it has in fact had the chance denied to other species. There are a good many, however, which would in that case be in the same category. Some years ago I received from time to time a very large number of earthworms from the Royal Gardens at Kew which had been accidentally imported thither from many quarters of the globe, among which I described some eighteen or twenty new species including, for instance, the African genus Gordiodrilus. There are plenty of facts of a similar nature and Dr Michaelsen has pointed out that botanical gardens act as centres of dispersion for accidentally introduced Oligochaeta. We must therefore come to the conclusion that temperature is at least one of the causes of a difference in the capability of extending their range shown by the Oligochaeta, a cause which doubtless operates as a check upon extension of range in non-peregrine forms also, and prevents for instance the dispersion of the tropical African Eudrilidae into the region of the Cape.
We may, as it appears to me, confidently look upon indifference to varying temperature as a condition of ability to colonise new countries. But it is obvious that this is not of itself a sufficient cause to explain the facts. Otherwise this country and N. Europe would contain many antarctic earthworms; the only one that has been recorded to my knowledge is Microscolex.
Though an inability to endure a temperate climate may have rendered the movements of peregrine species more limited, the same or rather the exactly opposite cause does not seem to have played any important part in this direction. For it is above all the Lumbricidae, normally dwellers in temperate climates, that are so remarkable for their wide range over the world. Nor can it be convincingly asserted that the extra-Palaearctic Lumbricids are real indigenes of those—often tropical—countries. For if so we should expect them to be at least of different species. Lumbricids however from South America, Australia, etc., are specifically identical with European forms.
There is no doubt that wherever land has been at all long under cultivation in any part of the world that land will be found to produce species of the European genera Lumbricus, Helodrilus, Eisenia, etc. More than this the recently imported European forms will be found to have largely or almost entirely driven out the native species, which have retired more into the interior of the country. There is thus here no barrier placed by temperature. It should be remarked, however, that while these earthworms are most abundant in the less tropical regions, they occur in such tropical districts as Peru, though in less striking numbers. Whether those of North America are really indigenes or not remains perhaps a matter for discussion; but it is at least noteworthy that the vast preponderance of species occurring there are also European and even British. In this particular case, which is on the whole the most emphatic of all the cases of peregrine earthworms, some explanations are possible, or at least have been offered. In the first place it would appear that earthworms are more abundant as individuals in northern countries where the soil is rarely dry for prolonged periods. And as has been already pointed out there is a close relation between earthworms and agriculture. Dunghills are fertile gathering grounds for some species, and ploughed fields and gardens always swarm with several species. In the tropics these animals are not so evident; and the strong rays of the sun appear to drive them further underground and into marshes; this obviously lessens the chance of their accidental transference by man. Furthermore Dr Eisen has pointed out that the European species are apt to have clitella and to be fertile all the year round, which is not always the case with other genera. That naturalist has added to this observation the fact that in rich cultivated soils in California it is impossible to find anything but imported European species, since cultivation itself appears actually to drive away the native forms.