210Pb, 226Ra and 137Cs were measured by non-destructive gamma spectrometry on marine sediment cores, collected during RIKEAU 2002 cruise on board r/v Thalia, on the shelf of the Bay of Biscay

In October 2019 we chose 15 sites from the 2019 EVHOE survey for environmental DNA (eDNA) sampling. The French international EVHOE bottom trawl survey is carried out annually during autumn in the BoB to monitor demersal fish resources. At each site, we sampled seawater using Niskin bottles deployed with a circular rosette. There were nine bottles on the rosette, each of them able to hold ∼5 l of water. At each site, we first cleaned the circular rosette and bottles with freshwater, then lowered the rosette (with bottles open) to 5 m above the sea bottom, and finally closed the bottles remotely from the boat. The 45 l of sampled water was transferred to four disposable and sterilized plastic bags of 11.25 l each to perform the filtration on-board in a laboratory dedicated to the processing of eDNA samples. To speed up the filtration process, we used two identical filtration devices, each composed of an Athena® peristaltic pump (Proactive Environmental Products LLC, Bradenton, Florida, USA; nominal flow of 1.0 l min–1 ), a VigiDNA 0.20 μm filtration capsule (SPYGEN, le Bourget du Lac, France), and disposable sterile tubing. Each filtration device filtered the water contained in two plastic bags (22.5 l), which represent two replicates per sampling site. We followed a rigorous protocol to avoid contamination during fieldwork, using disposable gloves and single-use filtration equipment and plastic bags to process each water sample. At the end of each filtration, we emptied the water inside the capsule that we replaced by 80 ml of CL1 conservation buffer and stored the samples at room temperature following the specifications of the manufacturer (SPYGEN, Le Bourget du Lac, France). We processed the eDNA capsules at SPYGEN, following the protocol proposed by Polanco-Fernández et al., (2020). Half of the extracted DNA was processed by Sinsoma using newly developped ddPCR assays for European seabass (Dicentrachus labrax), European hake (Merluccius merluccius) and blackspot seabream (Pagellus bogaraveo).  The other half of the extracted DNA was analysed using metabarcoding with teleo primer. The raw metabarcoding data set is available at https://www.doi.org/10.16904/envidat.442 Bottom trawling using a GOV trawl was carried out before or after water sampling. The catch was sorted by species and catches in numbers and weight were recorded. No blackspot seabream individuals were caught.   Data content: * ddPCR/: contains the ddPCR counts and DNA concentrations for each sample and species. * SampleInfo/: contains the filter volume for each eDNA sample. * StationInfo/: contains metadata related to the data collected in the field for each filter. * Metabarcoding/: contains metabarcoding results for teleoprimer. * Trawldata/: contains catch data in numbers and weight (kg).      

Aires géographiques des appellations d'origine contrôlées (AOC)/protégées (AOP). Le fichier liste pour chaque commune, identifiée par son département, son nom et son code INSEE, les aires géographiques des appellations AOC/AOP qui se situent sur la commune

The Commission for the Conservation Southern Bluefin Tuna collects a variety of data types from its Members and Cooperating Non-Members, including total catch, catch and effort data, and catch at size data. Catch, size and trade information is also collected through the Commission's Catch Documentation Scheme, Japanese import statistics, and other monitoring programs. Annual catches provided on this page are reported on a calendar year basis. CCSBT Members use quota years (not calendar years) for managing catching limits, but quota years differ between Members, so calendar years are used to provide catches on a common timescale. Relevant subsets and summaries of these data are provided below. All figures are subject to change as improved data or estimates become available. In particular, reviews of SBT data in 2006 indicated that southern bluefin tuna catches may have been substantially under-reported over the previous 10-20 years and the data presented here do not include estimates for this unreported catch. Also, data for the last reported year of catch (2020) are preliminary and are subject to revision. Any latitudes and longitudes presented in these summaries represent the north western corner of the relevant grid, which is a 5*5 grid unless otherwise specified. Other information on Members and Cooperating Non-Members fishing activities appears in the reports of the Extended Scientific Committee, Compliance Committee and Extended Commission.

This dataset gather isotopic ratios (carbon and nitrogen) and concentrations of mercury species (methyl and inorganic mercury) measured in several tissues (muscle, liver and gonad) for three commonly consumed fish species from the south Bay of Biscay (France) in 2017 and 2018.

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.  

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.

Global Fishing Watch is working across the globe to provide governments and authorities with actionable reports and capacity building to help strengthen fisheries monitoring and compliance. Our global team of experts produce analyses to inform monitoring, control and surveillance of fisheries in five key areas: - Illegal, unreported and unregulated fishing - Transshipment - Port controls - Marine protected areas - Operation support Collaboration and information sharing are integral to achieving well-managed fisheries. By working with stakeholders and making analyses available to national, regional and intergovernmental partners, Global Fishing Watch is enabling fisheries agencies to make more informed and cost-efficient decisions. Topics: - Commercial fishing, Global Fishing Watch is harnessing innovative technology to turn transparent data into actionable information and drive tangible change in the way that fisheries are governed. - Transshipment, Through publicly sharing map visualisations and creating data and analysis tools, we seek to inform management and policy efforts and provide a more complete picture of transshipment at sea. - Marine protected areas, Global Fishing Watch is harnessing the data and technology revolution to support the effective design, management and monitoring of marine protected areas.

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.