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.

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).

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.

The Level 4 merged microwave wind product is a complete set of hourly global 10-m wind maps on a 0.25x0.25 degree latitude-longitude grid, spanning 1 Jan 2010 through the end of 2020. The product combines background neutral equivalent wind fields from ERA5, daily surface current fields from CMEMS, and stress equivalent winds obtained from several microwave passive and active sensors to produce hourly surface current relative stress equivalent wind analyses. The satellite winds include those from recently launched L-band passive sensors capable of measuring extreme winds in tropical cyclones, with little or no degradation from precipitation. All satellite winds used in the analyses have been recalibrated using a large set of collocated satellite-SFMR wind data in storm-centric coordinates. To maximize the use of the satellite microwave data, winds within a 24-hour window centered on the analysis time have been incorporated into each analysis. To accomodate the large time window, satellite wind speeds are transformed into deviations from ERA5 background wind speeds interpolated to the measurement times, and then an optical flow-based morphing technique is applied to these wind speed increments to propagate them from measurement to analysis time. These morphed wind speed increments are then added to the background wind speed at the analysis time to yield a set of total wind speeds fields for each sensor at the analysis time. These individual sensor wind speed fields are then combined with the background 10-m wind direction to yield vorticity and divergence fields for the individual sensor winds. From these, merged vorticity and divergence fields are computed as a weighted average of the individual vorticity and divergence fields. The final vector wind field is then obtained directly from these merged vorticity and divergence fields. Note that one consequence of producing the analyses in terms of vorticity and divergence is that there are no discontinuities in the wind speed fields at the (morphed) swath edges. There are two important points to be noted: the background ERA5 wind speed fields have been rescaled to be globally consistent with the recalibrated AMSR2 wind speeds. This rescaling involves a large increase in the ERA5 background winds beyond about 17 m/s. For example, an ERA5 10 m wind speed of 30 m/s is transformed into a wind speed of 41 m/s, and a wind speed of 34 m/s is transformed into a wind speed of about 48 m/s. Besides the current version of the product is calibrated for use within tropical cyclones and is not appropriate for use elsewhere. This dataset was produced in the frame of ESA MAXSS project. The primary objective of the ESA Marine Atmosphere eXtreme Satellite Synergy (MAXSS) project is to provide guidance and innovative methodologies to maximize the synergetic use of available Earth Observation data (satellite, in situ) to improve understanding about the multi-scale dynamical characteristics of extreme air-sea interaction.

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.

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.

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.

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

This dataset provides the meridional and zonal components of both the stress-equivalent wind (U10S) and wind stress (Tau) vectors. The ERA* product is a correction of the ECMWF Fifth Reanalysis (ERA5) output by means of geo-located scatterometer-ERA5 differences over a 15-day temporal window. The product also contains ERA5 U10S and Tau. 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 ICM (Institute of Marine Sciences) / CSIC (Consejo Superior de Investigaciones Científicas) 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.