The GEBCO_2022 Grid is a global continuous terrain model for ocean and land with a spatial resolution of 15 arc seconds. In regions outside of the Arctic Ocean area, the grid uses as a base Version 2.4 of the SRTM15_plus data set (Tozer, B. et al, 2019). This data set is a fusion of land topography with measured and estimated seafloor topography. Included on top of this base grid are gridded bathymetric data sets developed by the four Regional Centers of The Nippon Foundation-GEBCO Seabed 2030 Project. The GEBCO_2022 Grid represents all data within the 2022 compilation. The compilation of the GEBCO_2022 Grid was carried out at the Seabed 2030 Global Center, hosted at the National Oceanography Centre, UK, with the aim of producing a seamless global terrain model. Outside of Polar regions, the Regional Centers provide their data sets as sparse grids i.e. only grid cells that contain data are populated. These data sets were included on to the base using a remove-restore blending procedure. This is a two-stage process of computing the difference between the new data and the base grid and then gridding the difference and adding the difference back to the existing base grid. The aim is to achieve a smooth transition between the new and base data sets with the minimum of perturbation of the existing base data set. The data sets supplied in the form of complete grids (primarily areas north of 60N and south of 50S) were included using feather blending techniques from GlobalMapper software. The GEBCO_2022 Grid has been developed through the Nippon Foundation-GEBCO Seabed 2030 Project. This is a collaborative project between the Nippon Foundation of Japan and the General Bathymetric Chart of the Oceans (GEBCO). It aims to bring together all available bathymetric data to produce the definitive map of the world ocean floor by 2030 and make it available to all. Funded by the Nippon Foundation, the four Seabed 2030 Regional Centers include the Southern Ocean - hosted at the Alfred Wegener Institute, Germany; South and West Pacific Ocean - hosted at the National Institute of Water and Atmospheric Research, New Zealand; Atlantic and Indian Oceans - hosted at the Lamont-Doherty Earth Observatory, Columbia University, USA; Arctic and North Pacific Oceans - hosted at Stockholm University, Sweden and the Center for Coastal and Ocean Mapping at the University of New Hampshire, USA.

The ESA Sea State Climate Change Initiative (CCI) project has produced global daily merged multi-sensor time-series of along-track satellite altimeter significant wave height data (referred to as Level 3 (L3) data) with a particular focus for use in climate studies. This dataset contains the Version 3 Remote Sensing Significant Wave Height product, which provides along-track data at approximately 6 km spatial resolution. It has been generated from upstream Sea State CCI L2P products, edited and merged into daily products, retaining only valid and good quality measurements from all altimeters over one day, with simplified content (only a few key parameters). This is close to what is delivered in Near-Real Time by the CMEMS (Copernicus - Marine Environment Monitoring Service) project. It covers the date range from 2002-2021. The altimeter data used in the Sea State CCI dataset v3 come from multiple satellite missions (Envisat, CryoSat-2, Jason-1, Jason-2, Jason-3, SARAL, Sentinel-3A), therefore spanning over a shorter time range than version 1.1. Unlike version 1.1, this version 3 involved a complete and consistent retracking of all the included altimeters. Many altimeters are bi-frequency (Ku-C or Ku-S) and only measurements in Ku band were used, for consistency reasons, being available on each altimeter but SARAL (Ka band).

Raw reads for the assembly of Gambusia holbrooki genome.

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.

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.

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 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.

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.

WGS for Iatlantic projet ( ) for assessing past and present connectivity