Ifremer Brest

Plouzané, France

Ifremer Brest

Plouzané, France
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Tivey M.A.,Woods Hole Oceanographic Institution | Barriga F.J.A.S.,University of Lisbon | Cherkashov G.,Saint Petersburg State Polytechnic University | Fouquet Y.,Ifremer Brest | And 8 more authors.
OCEANS'11 - MTS/IEEE Kona, Program Book | Year: 2011

The Seafloor Mineralization Working Group (SMWG) of the international non-profit organization InterRidge was formed is 2008 to address the issues surrounding the burgeoning interest in the mineral resources associated with hydrothermal vents found at the midocean ridge system. Following a successful workshop and colloquium on the issues surrounding deep sea mining at vent systems, the working group outlined some of the key science questions needed to better understand this complex system. © 2011 MTS.

Ramirez-Llodra E.,CSIC - Institute of Marine Sciences | Brandt A.,Biocentrum Grindel and Zoological Museum | Danovaro R.,Marche Polytechnic University | De Mol B.,University of Barcelona | And 12 more authors.
Biogeosciences | Year: 2010

The deep sea, the largest biome on Earth, has a series of characteristics that make this environment both distinct from other marine and land ecosystems and unique for the entire planet. This review describes these patterns and processes, from geological settings to biological processes, biodiversity and biogeographical patterns. It concludes with a brief discussion of current threats from anthropogenic activities to deep-sea habitats and their fauna. Investigations of deep-sea habitats and their fauna began in the late 19th century. In the intervening years, technological developments and stimulating discoveries have promoted deep-sea research and changed our way of understanding life on the planet. Nevertheless, the deep sea is still mostly unknown and current discovery rates of both habitats and species remain high. The geological, physical and geochemical settings of the deep-sea floor and the water column form a series of different habitats with unique characteristics that support specific faunal communities. Since 1840, 28 new habitats/ecosystems have been discovered from the shelf break to the deep trenches and discoveries of new habitats are still happening in the early 21st century. However, for most of these habitats the global area covered is unknown or has been only very roughly estimated; an even smaller - indeed, minimal - proportion has actually been sampled and investigated. We currently perceive most of the deep-sea ecosystems as heterotrophic, depending ultimately on the flux on organic matter produced in the overlying surface ocean through photosynthesis. The resulting strong food limitation thus shapes deep-sea biota and communities, with exceptions only in reducing ecosystems such as inter alia hydrothermal vents or cold seeps. Here, chemoautolithotrophic bacteria play the role of primary producers fuelled by chemical energy sources rather than sunlight. Other ecosystems, such as seamounts, canyons or cold-water corals have an increased productivity through specific physical processes, such as topographic modification of currents and enhanced transport of particles and detrital matter. Because of its unique abiotic attributes, the deep sea hosts a specialized fauna. Although there are no phyla unique to deep waters, at lower taxonomic levels the composition of the fauna is distinct from that found in the upper ocean. Amongst other characteristic patterns, deep-sea species may exhibit either gigantism or dwarfism, related to the decrease in food availability with depth. Food limitation on the seafloor and water column is also reflected in the trophic structure of heterotrophic deep-sea communities, which are adapted to low energy availability. In most of these heterotrophic habitats, the dominant megafauna is composed of detritivores, while filter feeders are abundant in habitats with hard substrata (e.g. mid-ocean ridges, seamounts, canyon walls and coral reefs). Chemoautotrophy through symbiotic relationships is dominant in reducing habitats. Deep-sea biodiversity is among of the highest on the planet, mainly composed of macro and meiofauna, with high evenness. This is true for most of the continental margins and abyssal plains with hot spots of diversity such as seamounts or cold-water corals. However, in some ecosystems with particularly "extreme" physicochemical processes (e.g. hydrothermal vents), biodiversity is low but abundance and biomass are high and the communities are dominated by a few species. Two large-scale diversity patterns have been discussed for deep-sea benthic communities. First, a unimodal relationship between diversity and depth is observed, with a peak at intermediate depths (2000-3000 m), although this is not universal and particular abiotic processes can modify the trend. Secondly, a poleward trend of decreasing diversity has been discussed, but this remains controversial and studies with larger and more robust data sets are needed. Because of the paucity in our knowledge of habitat coverage and species composition, biogeographic studies are mostly based on regional data or on specific taxonomic groups. Recently, global biogeographic provinces for the pelagic and benthic deep ocean have been described, using environmental and, where data were available, taxonomic information. This classification described 30 pelagic provinces and 38 benthic provinces divided into 4 depth ranges, as well as 10 hydrothermal vent provinces. One of the major issues faced by deep-sea biodiversity and biogeographical studies is related to the high number of species new to science that are collected regularly, together with the slow description rates for these new species. Taxonomic coordination at the global scale is particularly difficult, but is essential if we are to analyse large diversity and biogeographic trends. Because of their remoteness, anthropogenic impacts on deep-sea ecosystems have not been addressed very thoroughly until recently. The depletion of biological and mineral resources on land and in shallow waters, coupled with technological developments, are promoting the increased interest in services provided by deep-water resources. Although often largely unknown, evidence for the effects of human activities in deep-water ecosystems - such as deep-sea mining, hydrocarbon exploration and exploitation, fishing, dumping and littering - is already accumulating. Because of our limited knowledge of deep-sea biodiversity and ecosystem functioning and because of the specific life-history adaptations of many deep-sea species (e.g. slow growth and delayed maturity), it is essential that the scientific community works closely with industry, conservation organisations and policy makers to develop robust and efficient conservation and management options. © Author(s) 2010.

Etcheber H.,CNRS Laboratory of Oceanic Environments and Paleo-environments (EPOC) | Schmidt S.,CNRS Laboratory of Oceanic Environments and Paleo-environments (EPOC) | Sottolichio A.,University of Bordeaux 1 | Maneux E.,GEO Transfert ADERA | And 9 more authors.
Hydrology and Earth System Sciences | Year: 2011

The Gironde Estuary, one of the largest European ones, presents temporary low dissolved oxygen content in its fluvial section close to the Bordeaux urban area. In a context of population growth and of long-term environmental changes, the development of a high-frequency monitoring programme of the fluvial-estuarine system of the Gironde, called MAGEST (MArel Gironde ESTuary), had appeared essential to address current and future water-quality issues/evaluations. The objectives of the MAGEST survey program are to establish a reference database to improve the knowledge of the Gironde Estuary functioning, encompassing the aspects of hydrology, sediment dynamics and biogeochemistry. Through examples of results from intratidal to seasonal time scales, we demonstrate how such a long-term, high-frequency monitoring of a fluvio-estuarine system is of valuable interest to extract the main trends of its functioning and of the water quality in relation to external forcings (climatology, urban wastes, land use, ...) and to predict the future evolution of an estuary with global and environmental changes.

Bourdaud P.,Ifremer Center Manche Mer du Nord | Gascuel D.,Agrocampus Ouest | Bentorcha A.,Ifremer Brest | Brind'Amour A.,French Research Institute for Exploitation of the Sea
Ecological Indicators | Year: 2016

In the present study, we tested five trophic indicators and we demonstrated their usefulness to assess the environmental status of marine ecosystems and to implement an ecosystem approach to fisheries management (EAFM). The tested indicators include the slope of the biomass spectrum, the mean trophic level (MTL), the marine trophic index (MTI) and two newly developed indicators, the high trophic level indicator (HTI) and the apex predator indicator (API). Indicators are compared between current state and potential reference situations, using as case studies: the Celtic Sea/Bay of Biscay, North Sea and English Channel ecosystems. Trophic spectra are obtained from Ecopath models while reference situations are estimated, simulating with EcoTroph and Ecosim different fishing pressures including three candidate scenarios for an EAFM. Inter-ecosystems assessments are done using Ecopath models, simulations outputs and scientific surveys data to assess the current states of the studied ecosystems, contrast the reference situations and analyze the responses of all indicators. Sensitivity analyses are also conducted on the main simulation parameters to test the robustness of the chosen indicators. Ecosystems specific targets for EAFM are proposed for the five trophic indicators estimated from whole-ecosystem models, while in the Celtic Sea/Bay of Biscay ecosystem targets are proposed for the MTL (=3.85) and HTI (48%) estimated from standard bottom-trawl surveys. The HTI is proposed to be relevant for survey data and the API is recommended using whole-ecosystem models. We conclude that HTI and API show trends in ecosystems health better than MTI. © 2015 Elsevier Ltd.

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