USE OF TAPHONOMIC DATA ALONG WITH SPECIES COMPOSITION AS PROXIES FOR GRASS-BED CHARACTERISTICS: LARGE BENTHIC FORAMINIFERA, SAN SALVADOR, BAHAMAS
Six localities having a range of vegetation densities, water depths, and water-energies were selected. Grass-bed densities were measured by counting individual sea grasses and algae in 50x50cm grids. One hundred individuals of each of the major genera were collected from each locality, and the top 1cm of sediment was collected. Foraminifera were picked from the collected vegetation and from the 2.0-0.5mm sediment fractions. Live and dead foraminifera were counted from vegetation and sediment samples, and total foraminiferal density was recorded. Dead foraminifera were categorized by taphonomic condition. Cluster analysis was used to group sites according to foraminiferal data and by vegetation type.
Cornuspiramia, Sorites, and Planorbulina were the dominant live foraminifera found on the favored substrates, Thalassia and Halimeda. Sediment assemblages from the same sites were dominated by (dead) Archaias, Quinqueloculina/ Triloculina, and Valvulina. Cluster analysis showed that the sediment foraminiferal assemblages do not separate according to vegetation type. The density of tests in the sediment corresponds to vegetation density to some degree, but factors such as nutrient supply may play major roles. Thus the species composition and density of foraminifera alone do not accurately reflect the taxonomic composition and density of sea-grass beds.
In contrast, taphonomic condition is a consistent indicator of the presence and density of sea-grass beds. Lush stands of Thalassia protect delicate tests on the seafloor. Here altered tests are frequently encrusted, whereas breakage and abrasion are more common in higher energy, sand-dominated sparse beds. For these reasons, we suggest that taphonomic state be included in carbonate-platform foraminiferal studies.