Understanding the dynamics of species interactions for food (prey-predator, competition for resources) and the functioning of trophic networks (dependence on trophic pathways, food chain flows, etc.) has become a thriving ecological research field in recent decades. This empirical knowledge is then used to develop population and ecosystem modelling approaches to support ecosystem-based management. The TrophicCS data set offers spatialized trophic information on a large spatial scale (the entire Celtic Sea continental shelf and upper slope) for a wide range of species. It combines ingested prey (gut content analysis) and a more integrated indicator of food sources (stable isotope analysis). A total of 1337 samples of large epifaunal invertebrates (bivalve mollusks and decapod crustaceans), zooplankton, fish and cephalopods, corresponding to 114 species, were collected and analyzed for stable isotope analysis of their carbon and nitrogen content. Sample size varied between taxa (from 1 to 52), with an average of 11.72 individuals sampled per species, and water depths ranged from 57 to 516 m. The gut contents of 1026 fish belonging to ten commercially important species: black anglerfish (Lophius budegassa), white anglerfish (Lophius piscatorius), blue whiting (Micromesistius poutassou), cod (Gadus morhua), haddock (Melanogrammus aeglefinus), hake (Merluccius merluccius), megrim (Lepidorhombus whiffiagonis), plaice (Pleuronectes platessa), sole (Solea solea) and whiting (Merlangius merlangus) were analyzed. The stomach content data set contains the occurrence of prey in stomach, identified to the lowest taxonomic level possible. To consider potential ontogenetic diet changes, a large size range was sampled. The TrophicCS data set was used to improve understanding of trophic relationships and ecosystem functioning in the Celtic Sea. When you use the data in your publication, we request that you cite this data paper. If you use the present data set (TrophicCS) for the majority of the data analyzed in your study, you may wish to consider inviting at least one author of the core team of this data paper to become a collaborator /coauthor of your paper.

The SARWAVE project is developing a new sea state processor from SAR images to be applied over open ocean, sea ice, and coastal areas, and exploring potential synergy with other microwave and optical EO products.

The SARWAVE project is developing a new sea state processor from SAR images to be applied over open ocean, sea ice, and coastal areas, and exploring potential synergy with other microwave and optical EO products.

The diet and stable isotopic (i.e. δ15N and δ13C values) compositions of eels have been studied during each season of 2019 with a fyke net in six estuaries located along the French coast of the eastern English Channel (Slack, Wimereux, Liane, Canche, Authie and Somme estuaries) (10.1371/journal.pone.0270348).

Phenotypic plasticity, the ability of a single genotype to produce multiple phenotypes, is important for survival when species are faced with novel conditions. Theory predicts that range-edge populations will have greater phenotypic plasticity than core populations, but empirical examples from the wild are rare. The honeycomb worm, Sabellaria alveolata (L.), constructs the largest biogenic reefs in Europe, which support high biodiversity and numerous ecological functions. In order to assess the presence, causes and consequences of intraspecific variation in developmental plasticity and thermal adaptation in the honeycomb worm, we carried out common-garden experiments using the larvae of individuals sampled from along a latitudinal gradient covering the entire range of the species. We exposed larvae to three temperature treatments and measured phenotypic traits throughout development. We found phenotypic plasticity in larval growth rate but local adaptation in terms of larval period. The northern and southern range-edge populations of S. alveolata showed phenotypic plasticity for growth rate: growth rate increased as temperature treatment increased. In contrast, the core range populations showed no evidence of phenotypic plasticity. We present a rare case of range-edge plasticity at both the northern and southern range limit of species, likely caused by evolution of phenotypic plasticity during range expansion and its maintenance in highly heterogeneous environments. This dataset presents the raw image data collected for larval stages of Sabellaria alveolata from 5 populations across Europe and Northern Africa, exposed to 15, 20 and 25 C. Included are also opercular crown measurements used to estimate de size classes of individuals present in each population.  All measurements made with the images collected are presented in an Excel spreadsheet, also available here.

The French Atlantic coast hosts numerous macrotidal and turbid estuaries that flow into the Bay of Biscay that are natural corridors for migratory fishes. The two best known are those of the Gironde and the Loire. However, there are also a dozen estuaries set geographically among them, of a smaller scale. The physico-chemical quality of estuarine waters is a necessary support element for biological life and determines the distribution of species, on which many ecosystem services (e.g. professional or recreational fishing) depend. With rising temperatures and water levels, declining precipitation and population growth projected for the New Aquitaine region by 2030, the question of how the quality and ecological status of estuarine waters will evolve becomes increasingly critical. The MAGEST (Mesures Automatisées pour l’observation et la Gestion des ESTuaires nord aquitains) high-frequency monitoring of key physico-chemical parameters was first developed in the Gironde estuary in 2004 ; the Seudre and Charente estuaries were instrumented late 2020. First based on real-time automated systems, MAGEST is now equipped by autonomous multiparameter sensors. Depending of the stations, an optode is also deployed to secure dissolved oxygen measurement. By the end of 2020, MAGEST had 12 instrumented sites. Portets is a measuring station located in the upper Gironde estuary (Garonne subestuary, about 20 km upstream of the Bordeaux metropolis.

Serveur wms sur les photos anciennes

Global wave hindcast (1961-2020) at 1° resolution using CMIP6 wind and sea-ice forcings for ALL (historical), GHG (historical greenhouse-gas-only), AER (historical Anthropogenic-aerosol-only), NAT (historical natural only) scenario.

The ESA Sea State Climate Change Initiative (CCI) project has produced global multi-sensor time-series of along-track satellite synthetic aperture radar (SAR) integrated sea state parameters (ISSP) data from Sentinel-1 (referred to as SAR WV onboard Sentinel-1 Level 2P (L2P) ISSP data) with a particular focus for use in climate studies. This dataset contains the Sentinel-1 SAR Remote Sensing Integrated Sea State Parameter product (v1.0), which forms part of the ESA Sea State CCI version 3.0 release. This product provides along-track primary significant wave height measurements and secondary sea state parameters, calibrated with CMEMS model data and reference in situ measurements at 20km resolution every 100km, processed using the Pleskachevsky et. al., 2021 emprical model, separated per satellite and pass, including all measurements with flags and uncertainty estimates. These are expert products with rich content and no data loss. The SAR Wave Mode data used in the Sea State CCI SAR WV onboard Sentinel-1 Level 2P (L2P) ISSP v3 dataset come from the Sentinel-1 satellite missions spanning from 2014 to 2021 (Sentinel-1 A, Sentinel-1 B).

We genotyped 1680 thornback ray Raja clavata sampled in the Bay of Biscay using a DNA chip described in Le Cam et al. (2019). After quality control 4604 SNPs were retained for identifying potential sex-linked SNPs using three methods: i) identification of excess of heterozygotes in one sex, ii) FST outlier analysis between the two sexes and iii) neuronal net modelling. Genotype coding: 0 homozygous for major allele, 1 heterozygous, 2 homozygous for minor allele. Flanking DNA sequences of SNPs identified with methods i) and ii) are also provided.