Cold‐seep assemblages on a giant pockmark off West Africa: spatial patterns and environmental control

Marine Ecology - Tập 28 Số 1 - Trang 115-130 - 2007
Karine Olu1, Jean‐Claude Caprais1, A. Fifis1, Marie-Claire Fabri1, Joëlle Galéron1, Hélène Budzinsky2, Karyn Le Ménach2, Alexis Khripounoff1, Hélène Ondréas3, Myriam Sibuet1
1 Département Etude des Ecosystèmes Profonds (DEEP) IFREMER Centre de Brest, Plouzane, France
2 LPTC – UMR 5472 CNRS, Université Bordeaux I, 351, crs de la Libération, Talence, France
3 Département Geosciences Marines, Ifremer Centre de Brest, Plouzane, France

Tóm tắt

AbstractA giant pockmark colonised by dense cold‐seep assemblages near 3160 m depth along the Congo‐Angola margin has been surveyed by the ROV Victor 6000. The quantitative distribution of chemosynthetic communities was mapped along the dive tracks from a video study using GIS and image mosaicking. Several types of faunal assemblages, either dominated by bivalves of the families Mytilidae (Bathymodiolus sp.) or Vesicomyidae (Calyptogena sp., ‘Vesicomya’ aff. chuni), or by Siboglinidae polychaetes (Escarpia southwardae) were mapped over the 800‐m diameter pockmark area and sampled for fauna, water and sediment. The isotopic analyses (δ13C) of tissues from symbiont‐bearing species were within the range typical of nutrition via symbiosis using methane for mussels and sulphide for vesicomyids and siboglinids. The living chemosynthetic communities were distributed on a SW‐NE axis, corresponding to the expression at the sediment surface of a main buried channel providing fluids to the pockmark. The site was characterised by a more active central part in a depression with abundant carbonate concretions where high‐density clusters of siboglinids and mytilids dominate. Large fields of dead and live vesicomyids with a lower mean density were observed in the external areas. The mean coverage of each of the three symbiotic taxa in these two contrasted areas was estimated from mosaic analysis and was up to 30% in the central area dominated by E. southwardae bushes (23%). Symbiont‐bearing species distribution was consistent with methane concentrations in seawater that were generally higher in mytilid beds than in the vicinity of siboglinids and vesicomyids. A Principal Component Analysis performed on environmental factors at the ten sampling sites revealed that 37% of the observed variance in the distribution of symbiont‐bearing species may be explained by variation in both methane and oxygen concentrations, while a Canonical Redundancy Analysis selected methane concentration as the only variable which explains symbiont‐bearing species densities. This spatial distribution of chemosynthetic species at the pockmark scale may reflect temporal patterns of succession of both substrate and fauna, and may be related to different individual pockmarks visible on the microbathymetry mapped using ROV data.

Từ khóa


Tài liệu tham khảo

10.1007/BF01203716

Allais A‐G., 2004, Seabed Video Mosaicking with MATISSE: A Technical Overview and Cruise Results, 417

10.1139/z04-049

Barber A.J., 1986, Mud volcanoes, shale diapirs, wrench faults, and melanges in accretionary complexes, Eastern Indonesia, American Association of Petroleum Geologists Bulletin, 70, 1729

10.4319/lo.1997.42.2.0318

10.4319/lo.2006.51.3.1315

10.3354/meps241089

10.1016/S0022-0981(03)00046-7

10.3354/meps293099

10.1038/35036572

10.1016/j.chemgeo.2003.12.033

10.1016/S0967-0637(01)00060-7

Conway N.M., 1994, Stable Isotopes in the Study of Marine Chemosynthetic‐Based Ecosystems

Cosel Rv, 2002, A new species of bathymodioline mussel (Mollusca, Bivalvia, Mytilidae) from Mauritania (West Africa), with comments on the genus Bathymodiolus Kenk & Wilson, 1985, Zoosystema, 24, 259

10.3354/meps070049

10.1128/AEM.71.4.1694-1700.2005

Fonselius S, 1983, Methods of Seawater Analysis, 73

10.1144/GSL.SP.2003.216.01.12

10.1016/j.margeo.2005.09.011

10.1080/00364820310003190

10.1016/0012-821X(92)90098-G

Hovland M., 1988, Seabed Pockmarks and Seepages. Impact on Geology, Biology and the Marine Environment

Julian D., 1999, Roots as a site of hydrogen sulfide uptake in the hydrocarbon seep vestimentiferan Lamellibrachia sp, The Journal of Experimental Biology, 202, 2245, 10.1242/jeb.202.17.2245

Kasten S., 2001, Gas Hydrates in Surface Sediments of the Northern Congo Fan‐Geochemical and Microbiological Characterization of the Top of the Gas Hydrate Stability Zone, 1855

Kennicutt M.C., 1992, Stable isotope partitioning in seep and vent organisims: chemical and ecological significance, Chemical Geology, 101, 293

10.1080/00222930400002499

10.1201/9781420037449.ch1

10.3354/meps265123

10.3354/meps292051

10.1007/BF02431071

10.1016/S0025-3227(03)00098-7

10.1016/j.margeo.2005.09.007

10.1007/s003670050091

MoulinM. ContrucciI. OlivetJ.L. AslanianD. GéliL. SibuetJ. NouzeH. RéhaultJ. UnternehrP.(2002)Deep structures of the Angola margin. 27th European Geophysical Society Conference Nice France: 21–26 April.

Nadalig T., 2002, Structure and Diversity of Microbial Communities at Two Methane Seep Sites (Gulf of Guinea) 12th Annual Goldschmitt Conference

10.1007/BF01203723

10.1038/nature05227

10.1016/S0079-6611(97)00006-2

10.1016/S0967-0637(96)00123-9

10.1016/j.margeo.2005.09.011

10.1016/j.dsr.2004.07.004

Olu‐Le Roy K., 2005, Spatial Distribution and Nutritional Patterns of Megafauna on a Giant Pockmark in the Gulf of Guinea Third International Symposium on Hydrothermal Vent and Seep Biology

10.1007/s00367-005-0213-6

The R Development Core Team, 2004, The R Reference Manual – Base Package – Volumes 1 & 2

10.3354/meps231121

10.1039/ac9963300371

10.1007/BF01203722

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

10.4319/lo.1999.44.2.0334