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.

French Zostera Marina et Zostera Noltei abundance data are collected during monitoring surveys on the English Channel / Bay of Biscay coasts. Protocols are impletmented in the Water Framework Directive. Data are transmitted in a Seadatanet format (CDI + ODV) to EMODnet Biology european database. 35 ODV files have been generated from period 01/01/2004 to 31/12/2021 for Z. Marina and from 01/01/2011 to 31/12/2021 for Z. Noltei.  

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

This dataset provides detections of fronts derived from high resolution remote sensing SST observations by SEVIRI L3C from OSISAF over Western Europe 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).

French benthic invertebrates composition and abundance taxa data are collected during monitoring surveys on the English Channel / Bay of Biscay coasts and Mediterranean coast (Quadrige program code : REBENT_FAU, RSL_FAU). Protocols are implemented in the Water Framework Directive.  Data are transmitted in a Seadatanet format (CDI + ODV) to EMODnet Biology european database. 498 ODV files have been generated from period 01/01/2003 to 31/12/2021.

French intertidal and subtidal Macroalgae taxa data are collected during monitoring surveys on the English Channel / Bay of Biscay coasts.  Protocols are implemented in the Water Framework Directive. Data are transmitted in a Seadatanet format (CDI + ODV) to EMODnet Biology european database. 131 ODV files have been generated from period 01/01/2006 to 31/12/2021.

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.  

Reef-building species are recognized as having an important ecological role and as generally enhancing the diversity of benthic organisms in marine habitats.  However, although these ecosystem engineers have a facilitating role for some species, they may exclude or compete with others. The honeycomb worm Sabellaria alveolata (Linnaeus, 1767) is an important foundation species, commonly found from northwest Ireland to northern Mauritania (Curd et al., 2020), whose reef structures increase the physical complexity of the marine benthos, supporting high levels of biodiversity. Local patterns and regional differences in taxonomic and functional diversity were examined in honeycomb worm reefs from ten sites along the northeastern Atlantic to explore variation in diversity across biogeographic regions and the potential effects of environmental drivers. To characterize the functional diversity at each site, a biological trait analysis (BTA) was conducted (Statzner et al., 1994). Here we present the functional trait database used for the benthic macrofauna found to live in association with honeycomb worm reefs. Eight biological traits (divided into 32 modalities) were selected (Table 1), providing information linked to the ecological functions performed by the associated macrofauna. The selected traits provide information on: (i) resource use and availability (by the trophic group of species, e.g. Thrush et al. 2006); (ii) secondary production and the amount of energy and organic matter (OM) produced based on the life cycle of the organisms (including longevity, maximum size and mode of reproduction, e.g. (Cusson and Bourget, 2005; Thrush et al., 2006) and; (iii) the behavior of the species in general [i.e. how these species occupy the environment and contribute to biogeochemical fluxes through habitat, movement, and bioturbation activity at different bathymetric levels, e.g. (Solan et al., 2004; Thrush et al., 2006; Queirós et al., 2013). Species were scored for each trait modality based on their affinity using a fuzzy coding approach (Chevenet et al., 1994), where multiple modalities can be attributed to a species if appropriate, and allowed for the incorporation of intraspecific variability in trait expression. The information concerning polychaetes was derived primarily from Fauchald et al (1979) and Jumars et al (2015). Information on other taxonomic groups was obtained either from databases of biological traits (www.marlin.ac.uk/biotic) or publications (Naylor, 1972; King, 1974; Caine, 1977; Lincoln, 1979; Holdich and Jones, 1983; Smaldon et al., 1993; Ingle, 1996; San Martín, 2003; Southward, 2008; Gil, 2011; Leblanc et al., 2011; Rumbold et al., 2012; San Martín and Worsfold, 2015; Jones et al., 2018). Map indicating the locations of the 10 study sites in the UK, France and Portugal within the four biogeographic provinces defined by Dinter (2001). (All sites were sampled in 8 different stations, except for UK4 where 5 stations were sampled).

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.

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