Spatial heterogeneity of macrofaunal communities in and near a giant pockmark area in the deep Gulf of Guinea

Marine Ecology - Tập 31 Số 1 - Trang 78-93 - 2010
Lénaïck Menot1,2, Joëlle Galéron1, Karine Olu1, Jean‐Claude Caprais1, Philippe Crassous1, Alexis Khripounoff1, Myriam Sibuet2
1Ifremer, Département DEEP/LEP, Centre de Brest, Plouzané, France
2Institut Océanographique, Rue Saint Jacques, Paris, France

Tóm tắt

AbstractThe structure and familial‐level composition of macrofaunal communities were examined within and at distance from the giant pockmark Regab in the Southern Gulf of Guinea, at 3200 m depth. The two main questions addressed in this study were (i) does habitat partitioning by large symbiont‐bearing taxa influence macrofaunal assemblages and their environment? and (ii) to what extent does the chemosynthesis‐based ecosystem influence the structure and the composition of nearby macrobenthic communities? Along two radials, at sites from 250 to 1000 m away from the active centre of the cold seep, the abundance and composition of the macrofauna were typical of a deep‐sea community at that depth. Except for a few cores sampled in or near dead vesicomyid fields at the border of the pockmark area, the chemosynthetic ecosystem had no significant influence on macrofaunal communities beyond the edge of the giant pockmark. In seep sediments, the macrofauna had higher densities, reaching over 22,000 ind·m−2, but lower taxonomic richness than in background sediments. The polychaete assemblages associated with siboglinid tubeworms differed in their composition and vertical distribution from communities associated with vesicomyids or found at the border between vesicomyids and mytilids. The siboglinid habitat was dominated by surface‐feeders (ampharetids) or small carnivores (dorvilleids, hesionids and syllids) concentrated in the top sediment layer, while the vesicomyid beds were dominated by deep‐dwelling, subsurface feeders (capitellids and cossurids). This pattern may be related to bioturbation by the vesicomyids that allows an oxygenation of surface sediments while deepening down and enhancing the anaerobic oxidation of methane. Although alpha diversity of polychaete families is low in seep sediments, the variability of faunal assemblages and potentially high level of speciation in cold‐seep environments point to high beta diversity. Comparable numbers of polychaete families coexist in a quarter square meter of seep or non‐seep sediments, although the number of ecological niches that were sampled might be higher at seeps. Further integrative and comparative studies of the diversity and functioning of seep and non‐seep communities would certainly provide clues to understanding both ecosystems and their interactions.

Từ khóa


Tài liệu tham khảo

10.1139/z04-049

10.1016/S0022-0981(03)00046-7

10.3354/meps293099

10.1016/0967-0645(94)90051-5

10.1038/35036572

10.1016/j.dsr2.2009.04.007

10.1016/j.jembe.2006.07.017

10.1016/j.dsr.2007.01.001

10.1111/j.1439-0485.2009.00334.x

Cosel R. von, 2008, A new genus and new species of Vesicomyidae (Mollusca, Bivalvia) from cold seeps on the Barbados accretionary prism, with comments on other species, Zoosystema, 30, 929

Cosel R.V., 2009, Large Vesicomyidae (Mollusca: Bivalvia) from cold seeps in the Gulf of Guinea off the coasts of Gabon, Congo and northern Angola, Deep-Sea Research. Part II, Topical Studies in Oceanography

10.3354/meps165173

10.1016/j.gca.2008.02.016

Dinet A., 1985, Peuplements profonds du golfe de Gascogne: campagnes BIOGAS, 121

10.1016/S0967-0637(03)00052-9

10.1128/AEM.71.4.1694-1700.2005

10.1002/iroh.19950800212

10.1016/j.dsr2.2009.04.011

Gotelli N.J., 2009, Ecosim: Null Models Software for Ecology. Version 7

10.1086/285329

Hessler R.R., 1974, Abyssal community analysis from replicate box cores in the central North Pacific, Deep-Sea Research, 21, 185

10.3354/meps118187

10.1007/BF00390748

Jumars P.A., 1976, Deep‐sea species diversity: does it have a characteristic scale?, Journal of Marine Research, 34, 217

Jumars P.A., 1982, The Environment of the Deep‐Sea, 217

10.1007/s004420100716

Levin L.A., 2003, Oxygen minimum zone benthos: adaptation and community response to hypoxia, Oceanography and Marine Biology: an Annual Review, 41, 1

10.1201/9781420037449.ch1

10.1111/j.1439-0485.2006.00131.x

10.3354/meps208021

10.3354/meps265123

10.1016/j.jembe.2005.12.022

10.1111/j.1439-0485.2009.00335.x

10.3354/meps225065

10.1016/j.dsr2.2009.04.012

10.3354/meps257059

Oksanen J., 2008, Vegan: Community Ecology Package

10.1023/A:1022800405253

10.1111/j.1439-0485.2006.00145.x

10.1016/j.dsr2.2009.04.017

10.1007/s00367-005-0213-6

10.1016/0967-0637(95)00041-4

Pearson T.H., 1978, Macrobenthic succession in relation to organic enrichment and pollution of the marine environment, Oceanography and Marine Biology: an Annual Review, 16, 229

10.1111/j.1439-0485.2004.00034.x

10.3354/meps231121

10.1016/j.dsr.2003.08.004

10.1016/S0967-0645(97)00074-X

10.1007/978-3-662-05127-6_15

10.1016/j.dsr2.2009.04.015

Snelgrove P.V.R., 2002, A riot of species in an environmental calm; the paradox of the species‐rich deep sea, Oceanography and Marine Biology: an Annual Review, 40, 311

10.3354/meps059305

10.1023/A:1018513530268

10.3354/meps264001

10.1016/j.dsr2.2009.04.008