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Why and How Would a Welladapted Aquatic Plant Invade the Lan...

The answer seems to lie in the realization that for freshwater algae--the green algae are the most common freshwater forms--their habitat, when it consists of shallow ponds or streams, often, and even annually, dries out. Adaptations for surviving desiccation would be advantageous, and such adaptations would be preadaptations for living on land. When we consider the evolution of green algae in such terms, it is not improbable that terrestrial forms evolved. But we have no fossil evidence or other data to document that evolutionary breakthrough. There is a gap. It could well be another case of tachytelic evolution, wherein a form adapted to one adaptive zone invades a new zone, evolutionary changes are rapid, and no fossils are found. Furthermore the intermediates are not really successful aquatic plants nor are they successful land plants. They lose out in competition to both. Hence, no intermediates survive. But we cannot, from present information, document Lignier's hypothesis.

This again illustrates the frustrations of phylogenetic research: the concept of evolution encourages us to look for phyletic series, but the action of natural selection tells us we must both expect and accept gaps. Perhaps the most disconcerting aspect of such a gap is our lack of insight into how the primitive transport tissue--the stele--of Rhynia arose. It is disconcerting for two reasons. First, despite the relative simplicity of the rhyniophyte stele (it is a thin strand of long, slender cells in the middle of the stem), it makes a rather sud-den or genuinely neosemic appearance. It cannot be homologized with any green algae cells. Such apparently sudden and discontinuous changes, as we have emphasized, are inconsistent with the known process of evolutionary change. We can only hope that new data from living or fossil plants that represent a useful missing fink here will become available. The second reason is the origin of the nonvascular plants.

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