The Arcachon Bay is a unique and ecologically important meso-tidal lagoon on the Atlantic coast of south-west France. The Arcachon Bay has the largest area of dwarf seagrass (Z. noltei) in Europe, the extent of which was stable in their extent between the 1950s and 1990s, but a decline in seagrass was observed in mid-2000. The decline of Zostera (seagrass) may have a significant impact on sedimentation in this coastal ecosystem rich in marine life. Interface cores were collected in September 2022 to determine sediment and mass accumulation rates (SAR, MAR) in the Arcachon Bay. Ten study areas were selected, distributed over most of the areas where seagrass meadows are actually observed. Two sites were visited each time, one with the presence of Zostera noltei in good condition (Healthy) and the other where the sediment was bare (Bare). Maximum water heights during spring tides range from 3.44 m for the deepest site (Garrèche) to 2.09 m for the shallowest site (Fontaines). A total of 20 sediment cores were sampled and carefully extruded every 1 cm from the top to the bottom of the core. The sediment layers were used to determine dry bulk density and selected radioisotope activities: DBD, 210Pb, 226Ra, 137Cs, 228Th and 40K expressed as %K). 

The BioSWOT-Med campaign (Doglioli et al., 2023) was conducted aboard R/V L’Atalante from April 20 to May 15, 2023 in the Northwestern Mediterranean Sea, in the region of the North Balearic Front (NBF) to study interactions between fine-scale oceanic circulation and biogeochemical processes.  Three water masses were sampled across the NBF, northern ('A'), southern ('B'), and frontal ('F'). Each Lagrangian station consisted of a 24-hour sampling period following the displacement of a water parcel (Doglioli et al., 2024). Vertical profiles down to 500 m were collected every 6 hours at 06:00 ('T1'), 12:00 ('T2'), 18:00 ('T3'), and 00:00 ('T4') UTC, for a total of 28 Lagrangian stations: first between April~24-28 (A1, F1, B1), and again between May~4-7 (B2, F2, A2), with a final station in southern waters (B3) on May~12-13. B2 and B3 stations were located inside an anticyclonic eddy. Hydrological profiles were obtained using a Sea-Bird CTD, with data averaged to a 1~m vertical resolution, they include potential temperature (°C), practical salinity, fluorescence-derived chlorophyll-a (µg/L) and oxygen (µmol/kg).  Samples for nitrate + nitrite and phosphate (µM) were collected from Niskin bottles and analyzed onboard within 2-12~hours using a segmented flow analyzer (AAIII HR Seal Analytical) following (Aminot et al., 2007). Quantification limits (QL) were 0.05 µM for nitrate and 0.02 µM for phosphate. Phosphate concentrations at a nanomolar level analyses were performed in the laboratory using a high-sensitivity method combining a 1 m Liquid Waveguide Capillary Cell (LWCC) and an auto-analyzer (Zhang et al. 2002), achieving a detection limit of 0.002µM.  A BGC-Argo float (WMO: 1902605 - Provor CTS4 SUNA) equipped with a CTD and SUNA nitrate sensor was deployed near station B2 and sampled the anticyclonic eddy. To better resolve the photic and nutricline layers, the standard sampling cycle was modified to a 6-hour frequency, reaching depths of 300-400~m. The BGC-Argo float nitrate dataset spans May~2-16 and includes 55~profiles, with a 0.5 µM limit of quantification. It passed through a nitrate calibration procedure against 8 ship-made  profiles at B2 and B3. Data export in NetCDF format - Dataset at the 7 Lagrangian stations (28 vertical profiles for each variable, 4 at each station):  ‘BioSWOT-Med_LS_Date_Time.nc’ (with day, time, longitude and latitude);  ‘BioSWOT-Med_LS_Nutrients.nc’ (with nitrate, phosphate and phosphate at nanomolar level concentrations and depths);  'BioSWOT-Med_LS_CTD.nc' (with temperature in situ, practical salinity, chlorophyll-a and oxygen concentrations, photosynthetically active radiations and depth). - Dataset of the BGC-Argo float including 55 vertical profiles recorded between May 2 and 16:  'BioSWOT-Med_BGC-Argo' (with day and time, longitude, latitude; nitrate concentrations with associated depth; temperature in situ and practical salinity associated depth; chlorophyll-a concentrations with associated predepthssure; and oxygen concentrations with associated depth). Contact list  Aude Joël (aude.joel@mio.osupytheas.fr), Sandra Nunige (sandra.nunige@mio.osupytheas.fr, for ship-made nutrient dataset), Riccardo Martellucci (rmartellucci@ogs.it, for the BGC-Argo float dataset) and Andrea Doglioli (andrea.doglioli@mio.osupytheas.fr, for the BioSWOT-Med cruise). References Aminot, A., & Kérouel, R. 2007. Dosage automatique des nutriments dans les eaux marines: méthodes en flux continu. Méthodes d’analyse en milieu marin. Ifremer. Doglioli, A.M., & Gregori, G. 2023. BioSWOT-Med cruise, RV L’Atalante. doi:10.17600/18002392. Doglioli, A., Grégori, G., D’Ovidio, F., Bosse, P. E., A., Carlotti, F., Lescot, M.,. . . Waggonet, E. (2024). Bioswot med. biological applicati.ons of the satellite surface water and ocean topography in the mediterranean. ref. rapport de campagne. université aix-marseille. (doi:10.13155/100060) Zhang, J.Z., & Chi, J. 2002. Automated analysis of nanomolar concentrations of phosphate in natural waters with liquid waveguide. Environ Sci Technol., 1;36(5), 1048–53. doi: 10.1021/es011094v.  

In October 2019 we chose 15 sites from the 2019 EVHOE survey for environmental DNA (eDNA) sampling. The French international EVHOE bottom trawl survey is carried out annually during autumn in the BoB to monitor demersal fish resources. At each site, we sampled seawater using Niskin bottles deployed with a circular rosette. There were nine bottles on the rosette, each of them able to hold ∼5 l of water. At each site, we first cleaned the circular rosette and bottles with freshwater, then lowered the rosette (with bottles open) to 5 m above the sea bottom, and finally closed the bottles remotely from the boat. The 45 l of sampled water was transferred to four disposable and sterilized plastic bags of 11.25 l each to perform the filtration on-board in a laboratory dedicated to the processing of eDNA samples. To speed up the filtration process, we used two identical filtration devices, each composed of an Athena® peristaltic pump (Proactive Environmental Products LLC, Bradenton, Florida, USA; nominal flow of 1.0 l min–1 ), a VigiDNA 0.20 μm filtration capsule (SPYGEN, le Bourget du Lac, France), and disposable sterile tubing. Each filtration device filtered the water contained in two plastic bags (22.5 l), which represent two replicates per sampling site. We followed a rigorous protocol to avoid contamination during fieldwork, using disposable gloves and single-use filtration equipment and plastic bags to process each water sample. At the end of each filtration, we emptied the water inside the capsule that we replaced by 80 ml of CL1 conservation buffer and stored the samples at room temperature following the specifications of the manufacturer (SPYGEN, Le Bourget du Lac, France). We processed the eDNA capsules at SPYGEN, following the protocol proposed by Polanco-Fernández et al., (2020). Half of the extracted DNA was processed by Sinsoma using newly developped ddPCR assays for European seabass (Dicentrachus labrax), European hake (Merluccius merluccius) and blackspot seabream (Pagellus bogaraveo).  The other half of the extracted DNA was analysed using metabarcoding with teleo primer. The raw metabarcoding data set is available at https://www.doi.org/10.16904/envidat.442 Bottom trawling using a GOV trawl was carried out before or after water sampling. The catch was sorted by species and catches in numbers and weight were recorded. No blackspot seabream individuals were caught.   Data content: * ddPCR/: contains the ddPCR counts and DNA concentrations for each sample and species. * SampleInfo/: contains the filter volume for each eDNA sample. * StationInfo/: contains metadata related to the data collected in the field for each filter. * Metabarcoding/: contains metabarcoding results for teleoprimer. * Trawldata/: contains catch data in numbers and weight (kg).      

The ARCHYD dataset, which have been collected since 1988, represents the longest long-term hydrologic data sets in Arcachon Bay. The objectives of this monitoring programme are to assess the influence of oceanic and continental inputs on the water quality of the bay and their implications on biological processes. It also aims to estimate the effectiveness of management policies in the bay by providing information on trends and/or shifts in pressure, state, and impact variables. Sampling is carried on stations spread across the entire bay, but since 1988, the number and location of stations have changed slightly to better take into account the gradient of ocean and continental inputs. In 2005, the ARCHYD network was reduced to 8 stations that are still sampled by Ifremer to date. All the stations are sampled at a weekly frequency, at midday, alternately around the low spring tide and the high neap tide. Data are complementary to REPHY dataset. Physico-chemical measures include temperature, salinity, turbidity, suspended matters (organic, mineral), dissolved oxygen and dissolved inorganic nutrients (ammonium, nitrite+nitrate, phosphate, silicate). Biological measures include pigment proxies of phytoplankton biomass and state (chlorophyll a and phaeopigment).

This daily High-Resolution (HR) Level 3 gridded wind product is derived from Copernicus Sentinel-1 SAR (Synthetic Aperture Radar) observations, over the Mediterranean Sea ("MED" area). It is based on the European Space Agency (ESA) Level-2 OCN products at the highest available resolution. Although L2-OCN products already contain wind vectors, those are calculated using the CMOD5.n Geophysical Model Function (GMF) applied to the co-polarized (co-pol) VV channel (emitting in Vertical polarization and receiving in Vertical polarization). This VV GMF was mapped from scatterometer sensors (Hersbach et al., 2007) which are only able to use co-pol measurements. However, these co-pol GMF are known to lose sensitivity for wind above 20 m/s. Therefore, wind based on such GMF alone, are known to under-estimate wind speed (Polverari et al., 2022). For the L3 products winds based on SAR, we take advantage of the available cross-polarized (cross-pol) VH channel (emitting in Vertical polarization and receiving in Horizontal polarization) for which GMF were specifically derived based on C-Band SAR (Mouche et al., 2017, Mouche et al., 2019). Winds estimated from the combination of both the co-pol and cross-pol channels are referred to as dual-polarization (or dual-pol) winds. As shown in Mouche et al. (2019), taking advantage of the dual polarization strongly improves the wind estimation for high wind conditions thanks to the much greater VH channel sensitivity compared to VV. These new wind estimations are then gridded with a 0.012 degree resolution (between 0.5 and 1.2 km in zonal direction depending on the latitude and 1.3 km in meridional direction) using a cylindrical equidistant projection, independently for ascending and descending satellite passes and for each satellite (so 4 wind fields are available per day for two satellites). This dataset is generated over all Sentinel-1 mission time series starting from March 2018 and updated in delayed mode with a 4-months delay. It is also produced for 4 other different European areas. This dataset is produced and disseminated in the frame of Copernicus Marine Service.

This dataset contains the biological outputs of a global ocean simulation coupling dynamics and biogeochemistry at ¼° over the year 2019. The simulation has been performed using the coupled circulation/ecosystem model NEMO/PISCES (https://www.nemo-ocean.eu/), which is here enhanced to perform an ensemble simulation with explicit simulation of modeling uncertainties in the physics and in the biogeochemistry. This dataset is one of the 40 members of the ensemble simulation. This study was part of the Horizon Europe project SEAMLESS (https://seamlessproject.org/Home.html), with the general objective of improving the analysis and forecast of ecosystem indicators.   See Popov et al. (https://os.copernicus.org/articles/20/155/2024/) for more details on the study.

This dataset contains the dynamical outputs of a global ocean simulation coupling dynamics and biogeochemistry at ¼° over the year 2019. The simulation has been performed using the coupled circulation/ecosystem model NEMO/PISCES (https://www.nemo-ocean.eu/), which is here enhanced to perform an ensemble simulation with explicit simulation of modeling uncertainties in the physics and in the biogeochemistry. This dataset is one of the 40 members of the ensemble simulation. This study was part of the Horizon Europe project SEAMLESS (https://seamlessproject.org/Home.html), with the general objective of improving the analysis and forecast of ecosystem indicators.   See Popov et al. (https://os.copernicus.org/articles/20/155/2024/) for more details on the study.

Numerous reef-forming species have declined dramatically over the last century. Many of these declines have been insufficiently documented due to anecdotal or hard-to-access information. The Ross worm Sabellaria spinulosa (L.) is a tube-building polychaete that can form large mostly subtidal reefs, providing important ecosystem services such as coastal protection and habitat provision. It ranges from Scotland to Morocco and into the Mediterranean as far as the Adriatic, yet little is known about its distribution outside of the North & Wadden Seas, where it is protected under the OSPAR & HELCOM regional sea conventions respectively. As a result, online marine biodiversity information systems currently contain haphazardly distributed records of S. spinulosa. One of the objectives of the REEHAB project (http://www.honeycombworms.org) was to combine historical records with contemporary data to document changes in the distribution and abundance of the two Sabellaria species found in Europe, S. alveolata and S. spinulosa. Here we publish the result of the curation of 555 S. spinulosa sources, gathered from literature, targeted surveys, local conservation reports, museum specimens, personal communications by authors  their research teams, national biodiversity information systems (i.e. the UK National Biodiversity Network (NBN), www.nbn.org.uk) and validated citizen science observations (i.e. https://www.inaturalist.org). 56% of these records were not previously referenced in any online information system. Additionally, historic samples from Gustave Gilson were scanned for S. spinulosa information and manually entered.   The original taxonomic identification of the 40,261 S. spinulosa records has been kept. Some identification errors may however be present, particularly in the English Channel and Mediterranean where intertidal and shallow subtidal records can be mistaken for Sabellaria alveolata. A further 229 observations (16 sources) are recorded as ‘Sabellaria spp.’ as the available information did not provide an identification down to species level. Many sources reported abundances based on the semi-quantitative SACFOR scale whilst others simply noted its presence, and others still verified both its absence and presence. The result is a curated and comprehensive dataset spanning over two centuries on the past and present global distribution and abundance of S. spinulosa. Sabellaria spinulosa records projected onto a 50km grid. When SACFOR scale abundance scores were given to occurrence records, the highest abundance value per grid cell was retained.

Rapid changes in ocean circulation and climate have been observed in marine-sediment and ice cores over the last glacial period and deglaciation, highlighting the non-linear character of the climate system and underlining the possibility of rapid climate shifts in response to anthropogenic greenhouse gas forcing. To date, these rapid changes in climate and ocean circulation are still not fully explained. One obstacle hindering progress in our understanding of the interactions between past ocean circulation and climate changes is the difficulty of accurately dating marine cores. Here, we present a set of 92 marine sediment cores from the Atlantic Ocean for which we have established age-depth models that are consistent with the Greenland GICC05 ice core chronology, and computed the associated dating uncertainties, using a new deposition modeling technique. This is the first set of consistently dated marine sediment cores enabling paleoclimate scientists to evaluate leads/lags between circulation and climate changes over vast regions of the Atlantic Ocean. Moreover, this data set is of direct use in paleoclimate modeling studies.