Wide Range Of Morphological Diversity Research Articles

Tentacular diversity in deep-sea deposit-feeding holothurians: implications for biodiversity in the deep sea

The tentacles of deep-sea holothurians show a wide range of morphological diversity. The present paper examines gross tentacle morphology in surface deposit feeding holothurians from a range of bathymetric depths. Species studied included the elasipods: Oneirophanta mutabilis, Psychropotes longicauda and Benthogone rosea and the aspidochirotids: Paroriza prouhoi, Pseudostichopus sp., Bathyplotes natans and Paroriza pallens. The sympatric abyssal species Oneirophanta mutabilis, Psychropotes longicauda and Pseudostichopus sp. show subtle differences in diet and the structure and filling patterns of the gut that suggest differences in feeding strategies which may represent one mechanism to overcome competition for food resources in an environment where nutrient resources are considered to be, at least periodically, limiting. Interspecific differences in tentacle functional morphology and digestive strategies, which reflects taxonomic diversity could be explained in terms of Sanders'; Stability–Time Hypothesis. Since different tentacle types will turn over sediments to different extents, their impact on sedimentary communities will be enormous so that high diversity in meiofaunal communities may be explained most simply by Dayton and Hessler's Biological Disturbance Hypothesis.

Sexual reproduction in Acropora (Isopora) species (Coelenterata: Scleractinia)

Despite the wide range of morphological diversity among the Acropora (Isopora) colonies on Heron Island (Great Barrier Reef, Australia), only two reproductively isolated species were present from 1977 to 1982: A. cuneata (Dana, 1846) and A. palifera (Lamarck, 1816). Both species released planulae lacking zooxanthellae and were simultaneous hermaphrodites with testes and ovaries occurring on separate mesenteries within the same polyp. Oogenesis preceded spermatogenesis. Seasonal cycles of gametogenesis, embryogenesis and planulation occurred in the two species. Colonies of A. cuneata developed two cycles of gametes. One cycle matured near the first quarter moon in April and the other on the same lunar phase in June. Planulae release occurred from about September to December each year and was not correlated with lunar phase. Gametes of A. palifera ripened only once per annum, a few days after the last quarter moon in November, and planulation occurred from about January to March. Embryos were brooded in the coelenteron of the polyps in both species. Ova were fertilized in the mesenteries and embryos were retained within an envelope of mesoglea and gastrodermis, remaining attached to the mesentery by a stalk until the larvae matured and were released. A. palifera and A. cuneata were abundant in the unpredictable reef flat environment. However, their life-history traits, e.g. seasonal reproduction, delayed sexual maturity, large colony size and fairly long life span, were more specialised than had been predicted for this type of environment.