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.

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.

This dataset consists of metatranscriptomic sequencing reads corresponding to coastal micro-eukaryote communities sampled in Western Europe in 2018 and 2019.

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.

Wave impact is the primary cause of coastal structure failure. While wave impact is widely studied in controlled environments, in situ measurements of wave impact pressure are rare. The results of a campaign to measure wave impact pressure in situ are summarised here. Data were collected from 2016 to 2019 from anchored pressure gauges on the wall of the Artha breakwater in southwestern France. The acquisition frequency is 10 kHz and 10-minute bursts are recorded every hour. Two databases are published, one by burst and one by impact. The burst database summarises the main parameters describing the 10-minute record, while the impact database contains a list of parameters describing each impact.

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.

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.  

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

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.

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.