The ESA Sea State Climate Change Initiative (CCI) project has produced global multi-sensor time-series of along-track satellite altimeter significant wave height data (referred to as Level 4 (L4) data) with a particular focus for use in climate studies. This dataset contains the Version 3 Remote Sensing Significant Wave Height product, gridded over a global regular cylindrical projection (1°x1° resolution), averaging valid and good measurements from all available altimeters on a monthly basis (using the L2P products also available). These L4 products are meant for statistics and visualization. The altimeter data used in the Sea State CCI dataset v3 come from multiple satellite missions spanning from 2002 to 2021 ( 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).

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The ClimateFish database collates abundance data of 15 fish species proposed as candidate indicators of climate change in the Mediterranean Sea. An initial group of eight Mediterranean indigenous species (Epinephelus marginatus, Thalassoma pavo, Sparisoma cretense, Coris julis, Sarpa salpa, Serranus scriba, Serranus cabrilla and Caranx crysos) with wide distribution, responsiveness to temperature conditions and easy identification were selected by a network of Mediterranean scientists joined under the CIESM programme ‘Tropical Signals’ (https://www.ciesm.org/marine/programs/tropicalization.htm; Azzurro et al. 2010). Soon after, and thanks to the discussion with other expert groups and projects, C. crysos was no longer considered, and Lessepsian fishes (Red Sea species entering the Mediterranean through the Suez Canal) were included, namely: Fistularia commersonii, Siganus luridus, Siganus rivulatus, Pterois miles, Stephanolopis diaspros, Parupeneus forskali, Pempheris rhomboidea and Torquigener flavimaculosus. Considering the trend of increase of these species in the Mediterranean Sea (Golani et al. 2021) and their projected distribution according to climate change scenarios (D’Amen and Azzurro, 2020), more data on these tropical invaders are expected to come in the future implementation of the study. Data were collected according to a simplified visual census methodology (Garrabou et al. 2019) along standard transects of five minutes performed at a constant speed of 10m/min, corresponding approximately to an area of 50x5m. Four different depth layers were surveyed:  0-3m, 5-10 m, 11-20 m, 21-30 m. So far, the ClimateFish database includes fish counts collected along 3142 transects carried out in seven Mediterranean countries between 2009 and 2021, for a total number of 101'771 observed individuals belonging to the 15 fish species. Data were collected by a large team of researchers which joined in a common monitoring strategy supported by different international projects, which are acknowledged below. This database, when associated with climate data, offers new opportunities to investigate spatio-temporal effects of climate change in the Mediterranean Sea and test the effectiveness of each species as a possible climate change indicator.   Contacts: ernesto.azzurro(at)cnr.it   References: Azzurro E., Maynou F., Moschella P. (2010). A simplified visual census methodology to detect variability trends of coastal mediterranean fishes under climate change scenarios. Rapp. Comm. int. Mer Médit., 39. D’Amen, M. and Azzurro, E. (2020). Lessepsian fish invasion in Mediterranean marine protected areas: a risk assessment under climate change scenarios. ICES Journal of Marine Science, 77(1), pp.388-397. Garrabou, J., Bensoussan, N., Azzurro, E. (2019). Monitoring climate-related responses in Mediterranean marine protected areas and beyond: five standard protocols. Golani D.,  Azzurro E.,  Dulčić J.,  Massutí E., Orsi-Relini L.  (2021).  Atlas of Exotic Fishes in the Mediterranean Sea.  2nd edition  [F. Briand, Ed.]  365 pages.  CIESM Publishers, Paris, Monaco. ISBN number  978-92-990003-5-9   

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.

The CDR-derived Wet Tropospheric Correction (WTC) Product V2 is generated from the Level-2+ along-track altimetry products version 2024 (L2P 2024) distributed by AVISO+ (www.aviso.altimetry.fr). It provides a long-term, homogenized estimation of the wet tropospheric correction based on Climate Data Records (CDRs) of atmospheric water vapour combined with high frequencies MWR data. Two independent CDRs datasets are used: - REMSS V7R2 (coverage until 2022) https://www.remss.com/measurements/atmospheric-water-vapor/tpw-1-deg-product/ - HOAPS V5 precursor CDR from EUMETSAT CM SAF (coverage until 2020) HOAPS V4/V5 data available via https://wui.cmsaf.eu Note: the HOAPS V5 precursor is not yet an official CM SAF product; full validation and public release are pending. The MWR/CDR WTC V2 estimates is derived using spatially varying but temporally constant polynomial coefficients (ai). 1. WTC V2 – Along-track L2P Product Data format: The WTC V2 product is delivered in Level-2+ (L2P) format, along the satellite ground track. Each mission is distributed as a compressed archive (.tar.gz) containing one NetCDF4 CF-1.8 file per mission cycle. Archive naming convention: <mission>_WTC_from_WV_CDR_<version>.tar.gz mission: TP (TOPEX/Poseidon), J1, J2, J3 version: product version (currently V2) File naming convention inside archives: <mission>_C<cycle>.nc cycle: 4-digit cycle index (e.g., C0001) Each NetCDF file contains: 1/ Along-track WTC estimate; 2/ Ancillary information; 3/ Space–time coordinates 2. WTC CDR Uncertainties – Gridded Product: A complementary product is provided, delivering regional trend estimates and associated uncertainties from the WTC Climate Data Record. The uncertainty product is distributed as a single NetCDF4 file: wtc_trend_uncertainties.nc . This file contains global gridded fields of WTC CDR trend and uncertainty parameters. Product content: This is the first dedicated version providing both: WTC CDR (HOAPS) linear trends, and Uncertainty estimates on these trends. Uncertainties are expressed as 1-sigma confidence intervals, and propagated using the methodology described in Section 2.3 of the Product User Manual. The product includes: - Total uncertainty on the WTC trend, propagated from all identified uncertainty sources in the WTC–TCWV regression. - Individual contributions of uncertainty sources (Uncertainties on regression coefficients: a0, a1 and their standard deviations; Uncertainties inherited from the HOAPS TCWV CDR) These fields enable users to assess the relative importance of each uncertainty component and recompute uncertainty propagation with alternative methods. Included regression input variables: To ensure transparency and reproducibility, the product provides: 1/ regression coefficients a0, a1; 2/ their associated uncertainties (std of a0, std of a1); 3/additional diagnostic fields required to recompute uncertainties if needed.

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 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.

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

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).

Serveur wms du projet CHARM III