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In the mid-latitudes of the northeast Atlantic, the study of the upper branch of the AMOC is poorly documented. This study provides a complete record of the glacial, deglacial and Holocene dynamics of the easternmost portion of the upper branch of the AMOC, namely the European Slope Current and its glacial equivalent know as the Glacial Eastern Boundary Current (GEBC). To do so, we use core SU81-44 (~1000 m water depth) from the of southern Bay of Biscay (BoB) upper slope, .The aim of this study is to reconstruct paleoenvironmental and hydrodynamic changes using a multiproxy approach (i.e. benthic foraminiferal assemblage, grain size proxies, oxygen and carbon stable isotopes, and foraminiferal εNd). During the glacial period and the onset of the deglaciation, our results show that the grain size proxies together with the relative densities of the high-energy indicator species Trifarina angulosa and the low oxygen tolerant Globobulimina spp. showed significant fluctuations. These were concomitant with the main climate changes recognized over this period and with the glacial slope paleoflow reconstruction from the northern BoB. This highlights a strong climatic/oceanographic forcing on the sedimentary characteristics of the region and a prominent forcing by changes in near-bottom flow speed. Our data also provide a new constraint on the strength of the slope current in the region during the late deglaciation and Holocene periods. We observe a reinvigoration of the upper branch of the AMOC during the Bølling-Allerød warming, preceding the abrupt resumption of the deeper branch of the AMOC in the western North Atlantic. This seems to confirm the crucial role of the European Slope Current in deep water formation, as it is the case today. Finally, our data show a progressive weakening of the ESC during the Holocene and we hypothesize a link with the long-term dynamics of the subpolar gyre.
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The data file present detailed individual congener/compound concentrations for a large variety of hydrophobic organic contaminants including polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs), legacy and alternative brominated flame retardants (BFRs) and per- and polyfluoroalkyl substances (PFASs) in meso- and bathypelagic organisms collected in the Bay of Biscay, northeast Atlantic, in October 2017. The studied species include 3 crustacean species (Pasiphaea sivado, Sergia robusta, Ephyrina figueirai) and 11 fish species (Xenodermichthys copei, Searsia koefoedi, Myctophum punctatum, Notoscopelus kroeyeri, Lampanyctus crocodilus, Argyropelecus olfersii, Arctozenus risso, Stomias boa, Serrivomer beanii, Chauliodus sloani, Aphanopus carbo). The organisms were collected at night during one single trawling using a 25 m vertical opening pelagic trawl in the deep scattering layer (ca 800 m depth in the water column; 1330 m bottom floor). This dataset was used in the article entitled "A large diversity of organohalogen contaminants reach the meso- and bathypelagic organisms in the Bay of Biscay (northeast Atlantic)" published in Marine Pollution Bulletin.
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The ARCHYD dataset, which have been collected since 1988, represents the longest long-term hydrologic data sets in Arcachon Bay. The objectives of this monitoring programme are to assess the influence of oceanic and continental inputs on the water quality of the bay and their implications on biological processes. It also aims to estimate the effectiveness of management policies in the bay by providing information on trends and/or shifts in pressure, state, and impact variables. Sampling is carried on stations spread across the entire bay, but since 1988, the number and location of stations have changed slightly to better take into account the gradient of ocean and continental inputs. In 2005, the ARCHYD network was reduced to 8 stations that are still sampled by Ifremer to date. All the stations are sampled at a weekly frequency, at midday, alternately around the low spring tide and the high neap tide. Data are complementary to REPHY dataset. Physico-chemical measures include temperature, salinity, turbidity, suspended matters (organic, mineral), dissolved oxygen and dissolved inorganic nutrients (ammonium, nitrite+nitrate, phosphate, silicate). Biological measures include pigment proxies of phytoplankton biomass and state (chlorophyll a and phaeopigment).
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Sardine physiological measurments from september to november 2020
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This dataset gathers data used to infer the trophic structure and functioning of fish assemblages in the Eastern English Channel, the Bay of Biscay and the Gulf of Lions : - Biomass data, resulting from accoustic monitoring for pelagic species, or bottom trawling for demersal species, after extrapolation based on stratification scheme - Individual C and N isotopic ratios, length and mass, for all individuals considered - Individual energetic density values
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Since 2004, the Service facility SNAPO-CO2 (Service National d’Analyse des Paramètres Océaniques du CO2) housed by the LOCEAN laboratory (Paris, France) has been in charge for the analysis of Total Alkalinity (AT) and Total dissolved inorganic carbon (CT) of seawater samples on a series of cruises or ships of opportunity conducted in different regions in the frame of French projects. More than 44000 observations are synthetized in this work. Sampling was performed either from CTD-Rosette casts (Niskin bottles) or collected from the ship’s seawater supply (intake at about 5m depth). After completion of each cruise, discrete samples were returned back at LOCEAN laboratory and stored in a dark room at 4 °C before analysis generally within 2-3 months after sampling (sometimes within a week). AT and CT were analyzed simultaneously by potentiometric titration using a closed cell (Edmond, 1970). Certified Reference Materials (CRMs) provided by Pr. A. Dickson (Scripps Institution of Oceanography, San Diego, USA) were used to calibrate the measurements. The same instrumentation was used for underway measurements during OISO cruises (https://doi.org/10.18142/228) and OISO AT-CT data for 1998-2018 in the South Indian Ocean added in this synthesis. The synthesis is organized in two files (one for Global ocean and the Coastal Zones, one for the Mediterranean Sea) with the same format: Cruise name, Ship name, day, month, year, hour, minute, second, latitude, longitude, depth, AT (µmol/kg), Flag-AT, CT (µmol/kg), Flag-CT, Temperature (°C), Flag-Temp, Salinity (PSU), Flag-Salinity, nsample/cruise, nsample on file, sampling method.
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Key physico-chemical parameters (salinity, temperature, turbidity and dissolved oxygen) were measured in surface water during longitudinal transects in the Loire and Gironde estuaries in summers 2017 and 2018. This objective of this work was to determine the distribution of the dissolved oxygen and to detect potential severe desoxygenation. The transects were scheduled in order to begin the measurements at high tide from a site located upstream of an area where severe deoxygenation have been already been reported. Then, the transect was realised by sailing at low speed downstream with a multiparameter probe SAMBAT, maintained at 0.5 m below the surface, that collected a measurement every 2 minutes.
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Ifremer conducts numerous fisheries surveys dedicated to benthic and demersal populations (commercial / non-commercial fishes and invertebrates). For several years, in application of the ecosystem approach, all benthic invertebrate fauna collected in fishing gear has been systematically monitored: megabenthic invertebrates captured have been sorted, identified, counted and weighted. All these surveys are based on fixed or random stratified sampling strategy with varying intensity depending on the covered survey area. These data are stored, in historical access-based databases or for the most recent years in the centralised “Harmonie” database held in the Ifremer Fishery Information Systeme (SIH). The species nomenclature used was standardized using WoRMS database. Taxa caught at least once a year are listed for each monitoring area on the basis of already available data series. In order to facilitate the identification of individuals sampled on board vessels and to improve the training of onboard scientists, the present work aims to define the minimum level of identification for each of them. The analysis identifies taxa that appears recurrently on available historical series or gathers them on less precise taxonomic levels if this is not the case, which may indicate potential identification difficulties. The following procedure was used: all taxa expressed at the species level were first aggregated at genus level if they occurred less 90% of the years over the available time series. For MEDITS, EPIBENGOL and ORHAGO, the occurrence threshold was set to 70% and to only 50% for NOURMONT because the datasets were less than 10 years long. Then to be kept at that taxonomic level, a given genus had to be observed over 90% of the time (for example over at least 9 years if the dataset contains 10 years). Otherwise it was iteratively regrouped into a higher taxonomic level (family, order, class, division) following the same criteria (Foveau et al, 2017). For instance, for the NOURSEINE survey, this resulted into the aggregation of the 103 origin taxa into 35 taxonomic groups. The name of the final taxon after data processing represents the minimum level of identification defined by the analysis. However, these results are very theoretical. This is why they were sent to scientists who embark regularly in order to refine the level of taxonomic identification with field experience. The first dataset is composed of 8 tables relevant to the different vessel surveys. The first column of each table represents the permanent code of the taxon in the Ifremer taxonomic referential, the second the systematic number and the third the species abbreviated code. The other columns are the different taxonomic levels of the taxon. The minimum level of identification at sea defined by the data processing appears in blue. The level determined by feedback of scientist’s field experience, which is the one to use at sea, appears in green. The second dataset summaries the results detailed in the first table and indicates directly for each taxon identified to far, the minimum level of identification required for the benthic invertebrates by-catch of each fisheries surveys studied.
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Questions: Invasiveness depends in part on the ability of exotic species to either exclude native dominants or to fill an empty niche. Comparisons of niches and effects of closely related native and invasive species enable the investigation of this topic. Does Spartina anglica invade European salt marshes through competitive exclusion of the native Spartina maritima or due to the occurrence of an empty ecological niche in highly anoxic conditions? Location: The Arcachon Bay (France). Methods: At three intertidal levels, we quantified competitive response and effect abilities of the two species through a cross-transplantation removal experiment. We also compared at three intertidal levels the biomass, root/shoot ratio, productivity and environmental conditions (elevation, salinity, potential redox and soil moisture) of salt marsh communities dominated by the exotic Spartina anglica or the native Spartina maritima. Results: Both established species showed similar biotic resistance to the invasion of the other species, but the exotic showed important intraspecific facilitation for growth. Species had similar niches and total biomass along a gradient of anoxic conditions, but the exotic had a much higher root/shoot ratio and productivity than the native. Owing to its rhizome density, the exotic showed a high ability to increase sediment oxygenation, likely to explain its important intraspecific facilitation. Conclusions: Our results showed that the invasion success of S. anglica cannot be explained by the competitive exclusion of the native or by its ability to fill an empty niche along a gradient of anoxia. Its behaviour as a self-facilitator invasive engineer is very likely to explain its rapid spread in the Bay and biotic resistance to the colonization of other congeneric species when established in dense patches. Additionally, we suggest that physical disturbance in the marsh communities dominated by the native S. maritima may disrupt its biotic resistance against the invasion of S. anglica.
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The Mediterranean Sea is generally described as an oligotrophic area where primary productivity is limited to a few coastal environments with nutrient-enriched fluvial input. However, several studies have revealed that the hydrology of the western Mediterranean has major seasonal productive patterns linked either to significant riverine input or to seasonal upwelling cells. This study aims to: i) discuss organic microfossils (i.e. pollen and dinoflagellate cyst assemblages, as well as other non-pollen palynomorphs) from two different productive areas of the western Mediterranean Sea, and ii) examine the importance of the interconnections between marine and continental influences responsible for modern palynomorph distributions. Based on 25 samples from the Gulf of Lion (GoL) and Algerian Margin, this study key findings are: i) that GoL marine productivity is driven by the combination of discharges from the Rhône River and seasonal upwelling mechanisms, ii) that the strong productive pattern of the northern African coast is driven by water density front mixings and related upwellings. These two patterns are discussed in the light of major links that provide a better understanding of the signatures of marine and continental bio-indicators. The dinocyst Lingulodinium machaerophorum can be considered as a tracer of Rhône River plume influence in the GoL. Brigantedinium taxa are shown to be upwelling-sensitive in both studied areas. Typical differences in vegetation across the north–south climate gradient in the western Mediterranean Basin are highlighted by the larger ratio of Euro-Siberian to Mediterranean pollen taxa in the northern sector. Synoptic maps also illustrate the complex interactions of environmental drivers determining the distributions of continental and marine palynomorphs in the western Mediterranean Sea.
Catalogue PIGMA