A one-year survey of amphipods and tanaidaceans associated with monospecific sea grass meadows and a bare sand substratum, under similar physical-chemical conditions, showed that the magnozosterid Thalassia testudinum supported higher numbers of peracarids per square meter than the parvozosterid Halodule wrightii and the bare sand substratum as predicted by Kikuchi and Peres (1977). However, when examined in terms of numbers of individuals per unit sea grass biomass or surface area, Thalassia and Halodule supported nearly equal numbers ofepifauna. Syringodiumfiliforme, a syringodiid, consistently supported highest surface area-standardized abundances of epifauna. The previously reported significance of sea grass biomass in structuring crustacean assemblages held within, but not across, sea grass species. Although the amphipods and tanaids showed no species-specific association with sea grasses, the relative abundance of crustaceans was a function of both sea grass species and biomass. Relative abundance of infaunal types decreased from bare sand to Halodule to Syringodium to Thalassia sites and from low to high biomass sites. The abundance of peracarid crustaceans on sea grass meadows is a complex function of sea grass growth form and biomass which appear to mediate the distribution and foraging behavior of important predators. Despite evidence for strong parallelism among the animal communities of sea grass beds in different geographic regions (Ledoyer, 1964, 1969; Kikuchi, 1966, 1974; Nagle, 1968), Kikuchi and Peres (1977) pointed out that different sea grass species take distinct growth forms which affect the quality and nature of the habitat for small animals. Using the classification system of den Hartog (1967), the abundant sea grasses of the eastern United States are divided into magnozosterids (Zostera marina and Thalassia testudinum) with long, wide blades, parvozosterids (Halodule wrightil) with narrow blades, and syringodiids (Syringodium filiforme) with subulate blades. Because of high microhabitat diversity created by the wide blades, Kikuchi and Peres hypothesized that magnozosterids would support animal communities with higher biomass and species diversity than parvozosterids. Few studies have been designed to test for the role of sea grass species in the organization of associated fauna. Such a study requires closely spaced sites in monotypic beds of different sea grass species, all of which are characterized by similar physical-chemical conditions. In cases where conditions of station similarity have been met, significant differences were found in abundance, species composition, and species richness ofpolychaetes (Santos and Simon, 1974), crustaceans (Lewis, 1982), and fishes (Young, 1981; Stoner, in press) associated with different sea grass species. To test the hypothesis that various sea grass growth forms support different abundance and diversity of resident epifaunal organisms, peracaridan crustaceans were collected at seven closely spaced stations in Indian River lagoon, Florida. Three species of sea grass, Thalassia testudinum, Syringodiumfiliforme, and Halodule wrightii, represent the primary growth forms and are abundant in large beds in the lagoon. With care, it was possible to sample monospecific beds and bare sand substrata with similar depth and water conditions. Seasonal collections at the sites allowed an analysis of differences in species composition, faunal abun
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