This dataset gathers isotopic ratios (carbon and nitrogen) and concentrations of both priority (mercury species and polychlorinated biphenyls congeners) and emerging (musks and sunscreens) micropollutants measured in a host-parasite couple (hake Merluccius merluccius muscle and in its parasite Anisakis sp) from the south of Bay of Biscay in 2018. In addition, the hake infection degree measured as the number of Anisakis sp. larvae was added for each hake collected.

Particularly suited to the purpose of measuring the sensitivity of benthic communities to trawling, a trawl disturbance indicator (de Juan and Demestre, 2012, de Juan et al. 2009) was proposed based on benthic species biological traits to evaluate the sensibility of mega- and epifaunal community to fishing pressure known to have a physical impact on the seafloor (such as dredging and bottom trawling). The selected biological traits were chosen as they determine vulnerability to trawling: mobility, fragility, position on substrata, average size and feeding mode that can easily be related to the fragility, recoverability and vulnerability ecological concepts. The five categories retained are functional traits that were selected based on the knowledge of the response of benthic taxa to trawling disturbance (de Juan et al., 2009). They reflect respectively the possibility to avoid direct gear impact, to benefit from trawling for feeding, to escape gear, to get caught by the net and to resist trawling/dredging action, each of these characteristics being either advantageous or sensitive to trawling. To expand this approach to that proposed by Certain et al. (2015), the protection status of certain species was also indicated. To enable quantitative analysis, a score was assigned to each category: from low sensitivity (0) to high sensitivity (3). Biological traits of species have been defined, from the BIOTIC database (MARLIN, 2014) and from information given by Garcia (2010), Le Pape et al. (2007) and Brind’Amour et al. (2009). For missing traits, additional information from literature has been considered. The protection status of each taxa was also scored: Atlantic species listed in OSPAR List of Threatened and/or Declining Species and Habitats (https://www.ospar.org/work-areas/bdc/species-habitats/list-of-threatened-declining-species-habitats) and Mediterranean species listed in Vulnerable Marine Ecosystems (FAO, 2018 and Oceana, 2017) were scored 3 and other species were scored 1. The scores of 1085 taxa commonly found in bottom trawl by-catch in the southern North Sea, English Channel and north-western Mediterranean were described.

In order to better characterize the genetic diversity of Cetaceans and especially the common Dolphin from the Bay of Biscay, sequences from the mitochondrial Cytochrome B region were obtained from water samples acquired close to groups of dolphins.

This dataset provides detections of fronts derived from low resolution optimally interpolated remote sensing microwave SST L4 from REMSS over North Atlantic region. The data are available through HTTP and FTP; access to the data is free and open. In order to be informed about changes and to help us keep track of data usage, we encourage users to register at: https://forms.ifremer.fr/lops-siam/access-to-esa-world-ocean-circulation-project-data/ This dataset was generated by OceanDataLab and is distributed by Ifremer / CERSAT in the frame of the World Ocean Circulation (WOC) project funded by the European Space Agency (ESA).

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).

The SWISCA Level 2S (L2S) product provides along-track colocation of SWIM wave measuring instrument onto SCAT scatterometer grid, over the global ocean. SWIM and SCAT are both instruments onboard CFOSAT. CFOSAT (Chinese French Ocean SATellite) is a french-chinese mission launched in 2018, whose aim is to provide wind (SCAT instrument) and wave (SWIM instrument) measurements over the sea surface. The SWISCA L2S product is broken down into three different subproducts: - L2A containing the sigma0 of both SWIM and SCAT - L2B containing the wave parameters measured by SWIM and wind vectors measured by SCAT - AUX containing additional ancillary fields such as sea ice concentration (from CERSAT/SSMI), ocean currents (from CMEMS/GlobCurrent), SST and Wind (from ECMWF), rain rate (from IMERG), and WaveWatch3 wave spectra. All SWIM and ancillary observations are resampled onto SCAT scatterometer's geometry (wind vector cells, WVC). The SWISCA level 2S product is generated in delayed mode, a few days after acquisition. It is intended to foster cross analysis of SWIM and SCAT observations, and their combination to improve the retrieval of both wind and wave parameters. The SWISCA L2S product is generated and distributed by Ifremer / CERSAT in the frame of the Ifremer Wind and Wave Operation Center (IWWOC) co-funded by Ifremer and CNES and dedicated to the processing of the delayed mode data of CFOSAT mission.

This dataset provides surface Stokes drift as retrieved from the wave energy spectrum computed by the spectral wave model WAVEWATCH-III (r), under NOAA license, discretized in wave numbers and directions and the water depth at each location. It is estimated at the sea surface and expressed in m.s-1. WAVEWATCH-III (r) model solves the random phase spectral action density balance equation for wavenumber-direction spectra. Please refer to the WAVEWATCH-III User Manual for fully detailed description of the wave model equations and numerical approaches. The data are available through HTTP and FTP; access to the data is free and open. In order to be informed about changes and to help us keep track of data usage, we encourage users to register at: https://forms.ifremer.fr/lops-siam/access-to-esa-world-ocean-circulation-project-data/ This dataset was generated by Ifremer / LOPS and is distributed by Ifremer / CERSAT in the frame of the World Ocean Circulation (WOC) project funded by the European Space Agency (ESA).

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 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.

We developed a panel of single nucleotide polymorphism (SNP) markers for thornback ray Raja clavata using a RADSeq protocole. Demultiplexed sequences were aligned to the genome of Leucoraja erinacea which was used as reference genome. From an initial set of 389 483 putative SNPs, 7741 SNPs with the largest minor allele frequency were selected for implementation on an Infinium® XT iSelect-96 SNP-array implemented by LABOGENA DNA. For the array, SNPs [T/C] and [T/G] were replaced by those from the complementary strand [A/G] and [A/C] respectively. For some SNPs, a second SNP was found in the 50 nucleotide bases flanking sequence. In these cases, two SNP probes were developed with each of the two alleles of the second SNP. A SNP probe naming convention was adopted to identify these pairs of probes corresponding to the same SNP locus: “MAJ” or “MIN” followed by the corresponding base was included in the probe name. For some of these pairs, only one of the two markers could be developed, resulting in a total set of 9120 SNP probes, including 6360 single SNP probes, 10 MAJ or MIN probes for which a single probe was successfully developed, and 1375 pairs of probes with MAJ and MIN versions. The 9120 SNP genotypes were then scored using the clustering algorithm implemented in the Illumina® GenomeStudio Genotyping Analysis Module v2.0.3 for 7726 individual samples, including duplicates, mostly from the Bay of Biscay but also from the Mediterranean Sea and West Iberia. Overall, 1643 SNPs failed to be genotyped in all individuals, for 319 markers the minor allele was not found and 7158 markers (including 1974 for 987 MIN-MAJ pairs) produced bi-allelic genotypes. The majority of these SNPs had a minor allele frequency between 0.1 and 0.5. The MIN-MAJ probes can be used for quality checking the genotyping results