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Barnes D.K.A.; Bell, J.J. (2002). Coastal sponge communities of the West Indian Ocean: taxonomic affinities, richness and diversity. African Journal of Ecology. 40: 337-349.
9878
Barnes D.K.A.; Bell, J.J.
2002
Coastal sponge communities of the West Indian Ocean: taxonomic affinities, richness and diversity
African Journal of Ecology
40: 337-349
Publication
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Sponges assemblages were sampled in four coastal study regions (Malindi, Kenya; Quirimba Archipelago, northern Mozambique; Inhaca Island, Southern Mozambique and Anakao, Madagascar) in the west Indian Ocean. Sponge species were counted inmultiple 0.5m2 quadrats at depths of between 0 and 20m at a number of sites within localities within each region. Despite the relatively small areas sampled, sponge samples comprised a total of 130 species and 70 genera of the classes Demospongiae and Calcarea. Sponges are clearly a major taxon in these regions in terms of numbers of species, percentage cover or biomass, although their ecology in the west Indian Ocean is virtually unknown. Nearly half of the genera, e.g. Iotrochota, found were species with a so-called Tethyan distribution. Most of the other genera were cosmopolitan, e.g. Clathria, but some were coldwater (Coelosphaera), Indo-Australian (Ianthella) or circum-African (Crambe). Many of the species encountered in the present study occurred in at least two study regions, many in more and could occupy large areas of substratum. Some of these, e.g. Xestospongia exigua, are commonly found throughout the Indo-west Paci¢c region where they also occupy much space. The endemicity of the shallow water sponge faunas in East Africa (20^25%) seem to be high within the Indo-Pacific realm but are lower than northern Papua New Guinea. The tropical regions (Kenya and Northern Mozambique) were more speciose than subtropical regions (southern Mozambique and Madagascar) but not signi¢cantly more diverse (Shannon H0). Although latitude was not a major in£uence on sponge community patterns, hard substratum assemblages did form a cline from the tropics to Southern Mozambique, linked by Madagascar. Substratum nature (habitat) was most important in in£uencing the suite and number of species present. Sponge assemblages of soft substrata were much more dissimilar, both within and between habitats, than those on hard substrata. There was a predictable variability in species richness between hard substratum habitats: coral reefs being speciose and caves being less so. Our ¢ndings showed that both patterns and in£uences on species richness may be decoupled from those in£uencing diversity. In our data species richness, but not diversity, showed striking regional and bathymetric trends. In addition, sponge species richness mainly split at coral reef vs. non-reef habitats, whilst diversity divided principally into assemblages on hard and soft substrata.We consider this dichotomy of findings between species richness and diversity values to be important, as these are two principal measures used for the interpretation of biodiversity.
Indian Ocean, Western
Spacial and ecological distribution, Zonation, Microdistribution
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2013-01-12 18:30:12Z
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Plakinastrella Schulze, 1880 (additional source)
Anakao for Acanthella Schmidt, 1862 
Anakao for Aplysilla sulfurea Schulze, 1878  (inaccurate)
Anakao for Biemna Gray, 1867 
Anakao for Chondrilla nucula Schmidt, 1862  (inaccurate)
Anakao for Ciocalypta Bowerbank, 1862 
Anakao for Clathria Schmidt, 1862 
Anakao for Discodermia du Bocage, 1869 
Anakao for Dysidea Johnston, 1842 
Anakao for Haliclona Grant, 1841 
Anakao for Jaspis Gray, 1867 
Anakao for Petrosia Vosmaer, 1885 
Cosmopolitan (World Oceans) for Mycale Gray, 1867 
Inhaca Island for Aplysilla sulfurea Schulze, 1878  (inaccurate)
Inhaca Island for Ciocalypta Bowerbank, 1862 
Inhaca Island for Dysidea Johnston, 1842 
Inhaca Island for Haliclona Grant, 1841 
Inhaca Island for Jaspis johnstonii (Schmidt, 1862)  (inaccurate)
Inhaca Island for Petrosia Vosmaer, 1885 
Malindi for Aaptos Gray, 1867 
Malindi for Acanthella Schmidt, 1862 
Malindi for Biemna Gray, 1867 
Malindi for Callyspongia Duchassaing & Michelotti, 1864 
Malindi for Ciocalypta Bowerbank, 1862 
Malindi for Clathria Schmidt, 1862 
Malindi for Dysidea Johnston, 1842 
Malindi for Haliclona Grant, 1841 
Malindi for Iotrochota Ridley, 1884 
Malindi for Jaspis Gray, 1867 
Malindi for Jaspis johnstonii (Schmidt, 1862)  (inaccurate)
Malindi for Petrosia Vosmaer, 1885 
Quirimba Archipelago for Aaptos Gray, 1867 
Quirimba Archipelago for Aplysilla sulfurea Schulze, 1878  (inaccurate)
Quirimba Archipelago for Biemna Gray, 1867 
Quirimba Archipelago for Callyspongia Duchassaing & Michelotti, 1864 
Quirimba Archipelago for Ciocalypta Bowerbank, 1862 
Quirimba Archipelago for Clathria Schmidt, 1862 
Quirimba Archipelago for Dysidea Johnston, 1842 
Quirimba Archipelago for Haliclona Grant, 1841 
Quirimba Archipelago for Iotrochota Ridley, 1884 
Quirimba Archipelago for Jaspis Gray, 1867 
Quirimba Archipelago for Jaspis johnstonii (Schmidt, 1862)  (inaccurate)
Western and Northern Madagascar for Jaspis johnstonii (Schmidt, 1862)  (inaccurate)
World Oceans for Mycale Gray, 1867 
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