Concluding Remarks

Concluding Remarks

Concluding Remarks The bulk of secretory material necessary for the encapsulation of spermatozoa into a spermatophore is commonly derived from the male accessory organs of re­ production. Not surprisingly, the extraordinary diversity in size, shape, and struc­ ture of the spermatophores in different phyla is frequently a reflection of the equally spectacular variations in the anatomy and secretory performance of male reproductive tracts. Less obvious are the reasons why even within a given class or order of animals, only some species employ spermatophores, while others de­ pend on liquid semen as the vehicle for spermatozoa. The most plausible expla­ nation is that the development of methods for sperm transfer must have been in­ fluenced by the environment in which the animals breed, and that adaptation to habitat, rather than phylogeny, has played a decisive role. Reproduction in the giant octopus of the North Pacific, on which our attention has been focussed, pro­ vides an interesting example. During copulation in seawater, which may last 2 h, the sperm mass has to be pushed over the distance of 1 m separating the male and female genital orifices. The metre-long tubular spermatophore inside which the spermatozoa are conveyed offers an obvious advantage over liquid semen, which could hardly be hauled over such a long distance. Apart from acting as a convenient transport vehicle, the spermatophore serves other purposes. Its gustatory and aphrodisiac attributes, the provision of an ef­ fective barrier to reinsemination, and stimulation of oogenesis and oviposition are all of great importance. Absolutely essential is its function as storage organ for spermatozoa, at least as effective as that of the epididymis for mammalian spermatozoa. 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