(6) The probability that the arid climate of Peru is in our own time extending northward into Ecuador is pointed out; and from the presence of old coral blocks on the Peruvian beaches it is considered likely that when these corals throve the mangroves extended far down the coast of Peru.

(7) It is shown from the presence of the same species of mangroves on the Pacific and Atlantic coasts of America that there must have been, not long ago, a communication between these two oceans across Central America; but it is at the same time observed that this could not be inferred from shore-plants with buoyant seeds that, like Entada scandens, occur inland, since, although they occur on both sides of the continent, their distribution can be explained by the transport of their seeds by rivers to the Atlantic and Pacific coasts, such as we see in operation on the Panama isthmus in our own day.

(8) Stress is laid on the great development of mangroves in the Gulf of Guayaquil and in the Guayas estuary; and it is pointed out that there are in this locality two varieties of Rhizophora mangle, a large and a small variety, the first approaching in some of its characters the Asiatic species, R. mucronata, and being akin also to the seedless intermediate form of Fiji.

(9) Amongst other matters dealt with in this chapter are the floating seed-drift of the Guayas or Guayaquil River and the shore plants and stranded seed-drift of the Panama isthmus. From the locality last named we learn that rivers bring down from the interior to the Atlantic and Pacific coasts much the same seed-drift, and that from this centre littoral plants with buoyant seeds can be distributed over the whole tropical zone.

CHAPTER XXXIII
SEED-DISPERSAL AND GEOLOGICAL TIME

The shifting of the source of the Polynesian plants from the New to the Old World.—The floral history of Polynesia stated in terms of geological time.—The suspension of the agencies of dispersal in later periods.—Parallel differentiation in the course of ages of climate, bird, and plant.—New Zealand.—Insects and bats as agents in plant-dispersal.—The effective agency of sea-birds in other regions.—The observations of Ekstam.—The Spitzbergen controversy.—The efficacy of ducks as distributors of aquatic plants.—Summary.

In the matter of the dispersal of seeds by birds in the tropical Pacific, there are at least two questions which my readers must have frequently put to themselves. The one would be concerned with the shifting of the source of the Polynesian plants from America to the Old World, which occurred probably near the close of the Tertiary period. The other would be connected with the suspension of the work of dispersal over a large portion of Polynesia, which has become more and more pronounced as we approach our own day.

Suggested Cause of the Shifting of the Source of the Polynesian Plants from the New to the Old World.—In previous chapters we have discussed the various epochs in the plant-stocking of these islands. There was first the age of Coniferæ, in which the islands of the Western Pacific were only concerned, an age prior to the appearance of the volcanic groups of the Tahitian and Hawaiian regions, and placed in the Secondary period. Then followed, in the Tertiary period, after the birth of Hawaii and Tahiti, and when the island-groups of the Western Pacific were mainly submerged, the general dispersion from America of the Compositæ, Lobeliaceæ, and other orders, now represented only by genera peculiar to the Hawaiian and Tahitian islands. Last of all, towards the close of the Tertiary period, when the island-groups of the Western Pacific had re-emerged, a general dispersion of Old World plants, mainly Malayan, took place over all the present archipelagoes of the tropical Pacific.

Since the climate of Hawaii must have, to a great extent, shared in the vicissitudes of the continental climates of the northern hemisphere before, during, and after the Glacial epoch, it is assumed that in the Ice Age no tropical plants reached the group, and that only the plants now represented in its mountain-flora could have then reached there. The area of active dispersion of tropical plants was pushed far south. During the Ice period, Indo-Malayan plants doubtless crowded into the equatorial region of the Western Pacific; but, cramped and confined within this limited area, they were cut off by a climatic barrier from the cool latitudes of Hawaii. As the cold ages passed away, migratory birds, confined during that period to the southern hemisphere, would extend their ranges north, sometimes reaching Hawaii, and transporting to it the seeds of New Zealand and Antarctic genera, now represented by endemic species on its mountain-slopes. The Indo-Malayan plants, with the increasing warmth in the climate of the northern hemisphere, would overrun the Pacific, set free from their prison in the south-west portion of that ocean. Dispersal, we might imagine, would be at first very active over the whole ocean.

My point is, then, that whilst the Malayan era of the plant-stocking began after the Ice Age in the northern hemisphere, the dispersion of the New Zealand and Antarctic genera over the Pacific took place during that period; whilst, as before noticed, the dispersion of the Compositæ, Lobeliaceæ, and other orders, represented now in Hawaii by endemic genera, would be pre-Glacial and well back in the Tertiary epoch. I would, therefore, suggest the following scheme, in illustration of the floral history of the tropical Pacific.