This set of data documents the radiocarbon dates (n=19) obtained thanks to the accelerator mass spectrometry method (AMS) at the LMC14/ARTEMIS French national facility on the cores (Multicorer, Kullenberg) retrieved from the West-Gironde mud patch (WGMP) during the JERICObent-7 cruise (10-15 July 2019; NR Côtes de la Manche, https://doi.org/10.17600/18001022). The WGMP registers very high sedimentation rates since the last 600 years (≥ 0.3 cm/yr) and is thus of great interest for palaeoceanographic investigations. At present, this depocenter marks the mid-shelf of the temperate Bay of Biscay off major French rivers from the Aquitaine basin. The fine mud deposits of the WGMP are of 3 to 4 meters thick and lie on palimpsest levels rich in gravels and shells. They cover a V-shaped structure, oriented SW-NE, which is attributed to the incision(s) of a paleovalley in the Cenozoic substrate, mainly linked to the paleo-Gironde routing changes during past glacials/interglacials, and its potential past convergences with the paleo-rivers of the Antioche perthuis (Seudre, Charente paleovalleys?) at that times. Detailed information on each sample is presented with the 14C results obtained by the Artemis AMS facility at LMC14 laboratory (Dumoulin et al. 2017- https://doi.org/10.1017/RDC.2016.116, Beck et al. 2024- https://doi.org/10.1017/RDC.2023.23). Raw ages are indicated together with calibration calculations using the last two versions of the Calib software (http://calib.org/, Calib 7 and 8) to show the dispersion of ages linked to the updating of calibration curves (Marine13, Intcal13, Marine20, Intcal 20). The calibrated ages finally retained for publications (used in the related Seanoe document - https://doi.org/10.17882/104237 - and published in Eynaud et al., 2025 for the ST3c core, https://doi.org/10.1016/j.gloplacha.2025.105039) are those obtained with the last Calib 8.1 version. Raw 14C ages were calibrated and converted to calendar ages using the IntCal20 calibration curve with a reservoir age correction of 400 years deduced from Radionuclide analyses (137Cs and 210Pb) at the top of the studied cores (see Schmidt, 2025, https://www.seanoe.org/data/00968/107979/). 

Sardine physiological measurments from september to november 2020

Survival was recorded at the endpoint for all batches of each group (2n-control, 2n-wild, 2n-commercial, 2nR, 3nR and 3n-commercial). Similarly, initial and final yield were recorded, corresponding to the total weight of the live oysters at deployment and at the endpoint. Finally, shell length and total weight for individually recorded at reception and at the endpoint.

Ifremer conducts numerous fisheries surveys dedicated to benthic and demersal populations (commercial / non-commercial fishes and invertebrates). For several years, in application of the ecosystem approach, all benthic invertebrate fauna collected in fishing gear has been systematically monitored: megabenthic invertebrates captured have been sorted, identified, counted and weighted. All these surveys are based on fixed or random stratified sampling strategy with varying intensity depending on the covered survey area. These data are stored, in historical access-based databases or for the most recent years in the centralised “Harmonie” database held in the Ifremer Fishery Information Systeme (SIH). The species nomenclature used was standardized using WoRMS database. Taxa caught at least once a year are listed for each monitoring area on the basis of already available data series. In order to facilitate the identification of individuals sampled on board vessels and to improve the training of onboard scientists, the present work aims to define the minimum level of identification for each of them. The analysis identifies taxa that appears recurrently on available historical series or gathers them on less precise taxonomic levels if this is not the case, which may indicate potential identification difficulties. The following procedure was used: all taxa expressed at the species level were first aggregated at genus level if they occurred less 90% of the years over the available time series. For MEDITS, EPIBENGOL and ORHAGO, the occurrence threshold was set to 70% and to only 50% for NOURMONT because the datasets were less than 10 years long. Then to be kept at that taxonomic level, a given genus had to be observed over 90% of the time (for example over at least 9 years if the dataset contains 10 years). Otherwise it was iteratively regrouped into a higher taxonomic level (family, order, class, division) following the same criteria (Foveau et al, 2017). For instance, for the NOURSEINE survey, this resulted into the aggregation of the 103 origin taxa into 35 taxonomic groups. The name of the final taxon after data processing represents the minimum level of identification defined by the analysis. However, these results are very theoretical. This is why they were sent to scientists who embark regularly in order to refine the level of taxonomic identification with field experience. The first dataset is composed of 8 tables relevant to the different vessel surveys. The first column of each table represents the permanent code of the taxon in the Ifremer taxonomic referential, the second the systematic number and the third the species abbreviated code. The other columns are the different taxonomic levels of the taxon. The minimum level of identification at sea defined by the data processing appears in blue. The level determined by feedback of scientist’s field experience, which is the one to use at sea, appears in green. The second dataset summaries the results detailed in the first table and indicates directly for each taxon identified to far, the minimum level of identification required for the benthic invertebrates by-catch of each fisheries surveys studied.

Questions: Invasiveness depends in part on the ability of exotic species to either exclude native dominants or to fill an empty niche. Comparisons of niches and effects of closely related native and invasive species enable the investigation of this topic. Does Spartina anglica invade European salt marshes through competitive exclusion of the native Spartina maritima or due to the occurrence of an empty ecological niche in highly anoxic conditions? Location: The Arcachon Bay (France). Methods: At three intertidal levels, we quantified competitive response and effect abilities of the two species through a cross-transplantation removal experiment. We also compared at three intertidal levels the biomass, root/shoot ratio, productivity and environmental conditions (elevation, salinity, potential redox and soil moisture) of salt marsh communities dominated by the exotic Spartina anglica or the native Spartina maritima. Results: Both established species showed similar biotic resistance to the invasion of the other species, but the exotic showed important intraspecific facilitation for growth. Species had similar niches and total biomass along a gradient of anoxic conditions, but the exotic had a much higher root/shoot ratio and productivity than the native. Owing to its rhizome density, the exotic showed a high ability to increase sediment oxygenation, likely to explain its important intraspecific facilitation. Conclusions: Our results showed that the invasion success of S. anglica cannot be explained by the competitive exclusion of the native or by its ability to fill an empty niche along a gradient of anoxia. Its behaviour as a self-facilitator invasive engineer is very likely to explain its rapid spread in the Bay and biotic resistance to the colonization of other congeneric species when established in dense patches. Additionally, we suggest that physical disturbance in the marsh communities dominated by the native S. maritima may disrupt its biotic resistance against the invasion of S. anglica.

Marine microfossils (dinoflagellate cysts and planktonic foraminifera) and geochemical (XRF-Ti/Ca)-based climatic records from a core located off the Fleuve Manche (FM) paleo-mouth (MD13-3438) have revealed that sustained warm summer sea surface temperatures (SSTs) during sub-millennial climate changes within HS1 (~18–14.7 ka) may have played a key role in the FM regime related to the European Ice Sheet (EIS) melting rate. In this study, we have analyzed the MD13-3438 pollen content over the HS1 at a mean resolution of ~50 years to test whether vegetation-based air temperatures were coupled to SSTs face to this rapid climate variability. First, our results highlight two major phases of pollen sources at site MD13-3438, preventing the pollen record to be interpreted as a continuous record of the evolution of vegetation and climate occupying a single watershed across HS1. The first phase, i.e. the HS1-a interval (~18–16.8 ka), is marked by strong occurrences of boreal pollen taxa (especially Picea-Abies). Considering their spatial distribution and the coalescence of the British and Scandinavian ice sheets into the North Sea during the Last Glacial Maximum, these taxa probably originated from the North European Plain, i.e., eastern FM tributaries (east of the Rhine River), where cool-humid conditions generally prevailed. Then, the second phase, i.e. the HS1-b interval (~16.8–14.7 ka BP), is characterized by a deceleration of the EIS retreat and the drop of boreal pollen values at site MD13-3438 further signing a less influence of the upstream FM drainage system and thus a better characterization of pollen sources related with western FM tributaries. Superimposed to these two HS1 main phases, pollen fluctuations are concomitant with sub-millennial variability in the EIS deglaciation intensity. During the early HS1 (HS1-a), we discussed two short-term increases in the ratio between deciduous trees (Quercus-Corylus-Alnus) and herbaceous plants (Plantago-Amaranthaceae-Artemisia). These events were coeval with phases of increasing FM meltwater runoff and SST seasonality (i.e., dinocyst-based summer SST amplification). We associated these events with lower contribution of the upstream FM catchment as well as, possibly, atmospheric warming and regional sea-level positive oscillations. The HS1-b is composed of three main phases that appear more influenced by the downstream FM drainage system. HS1-b1 (16.8–16.3 ka BP) corresponds to the driest and coldest conditions west of the Rhine River. HS1-b2 (16.3–15.6 ka BP) is coeval with large arrivals of iceberg from the Hudson strait in the Bay of Biscay and thus likely to a major sea-level positive oscillation associated with a phase of FM valley reworking. HS1-b3 (15.6–14.7 ka BP) corresponds to persistent arid conditions that preceded the subsequent more humid conditions recorded from 14.7 ka BP at the start of the Bölling-Alleröd.

The West Gironde Mud Patch (WGMP) is a 420-km2 mud belt in the Bay of Biscay, located 25 km off the mouth of the Gironde estuary. This clay-silt feature of 4 m in thickness extends between 30 and 75m water depth, surrounded by the sands and gravels that cover the North Aquitaine continental shelf. Interface cores were collected during JERICOBent-1 cruise (October 2016; Deflandre (2016) doi.org/10.17600/16010400) along two cross-shelf transects for a total of 9 sites. Each sediment core was carefully extruded every 0.5 cm from the top core to 4 cm and every 1 cm below until the core bottom. The sediment layers were used to determine dry bulk density, grain size and selected radioisotope activities (210Pb, 226Ra, 137Cs, 228Th, K).

Key physico-chemical parameters (salinity, temperature, turbidity and dissolved oxygen) were measured in surface water during longitudinal transects in the Loire and Gironde estuaries in summers 2017 and 2018. This objective of this work was to determine the distribution of the dissolved oxygen and to detect potential severe desoxygenation. The transects were scheduled in order to begin the measurements at high tide from a site located upstream of an area where severe deoxygenation have been already been reported. Then, the transect was realised by sailing at low speed downstream with a multiparameter probe SAMBAT, maintained at 0.5 m below the surface, that collected a measurement every 2 minutes.

As part of the European Horizon Europe FOCCUS project (https://foccus-project.eu/), the metadata inventory of European coastal platforms has been extracted. The inventory was based on the following History and Latest products, downloaded from the CMEMS website (https://marine.copernicus.eu/fr/acces-donnees) at: 1) Global Ocean-In-Situ Near-Real-Time Observation, 2) Atlantic Iberian Biscay Irish Ocean-In-Situ Near Real Time Observations, 3) Mediterranean Sea-In-Situ Near Real Time Observations, 4) Atlantic-European North West Shelf-Ocean In-Situ Near Real Time Observations. To carry out this inventory, it was decided to target only coastal platforms, located less than 200km from the coast and at a depth of less than 400m. For mobile platforms, it was also decided to focus only on the first position in the file. This data must be located within 200 km of the coast and at a depth of less than 400 m. In this inventory, FerryBox platforms have all been considered as coastal platforms. The following platforms were extracted from the products: BO (Bottles), CT (CTD), DB (Drifting Buoys), FB (Ferry Box), GL (Gliders), HF (High Frequency Radar), MO (Mooring), PF (Profiling Float), TG (Tide Gauge) and XB (XBT). Once the metadata had been extracted from the files, duplicates were removed (files with the same names). Duplicate platforms of type _TS_ and _WS_ were merged (date and parameters). Latest‘ files have been merged with ’History" files. Missing metadata have been replaced in the Excel file by ‘Missing Data’. Some old dates were also revised by hand because they had been badly extracted, as well as some institution names that included special characters. Platforms located on estuaries/rivers/lakes/ponds have also been removed by hand. This inventory identified a total of 10,479 coastal platforms.

Particularly suited to the purpose of measuring the sensitivity of benthic communities to trawling, a trawl disturbance indicator (de Juan and Demestre, 2012, de Juan et al. 2009) was proposed based on benthic species life history traits to evaluate the sensibility of mega- and epifaunal community to fishing pressure known to have a physical impact on the seafloor (such as dredging and bottom trawling). The selected biological traits were chosen as they determine vulnerability to trawling: mobility, fragility, position on substrata, average size and feeding mode that can easily be related to the fragility, recoverability and vulnerability ecological concepts. Life history traits of species have been defined from the BIOTIC database (MARLIN, 2014) and from information given by Le Pape et al. (2007), Brindamour et al. (2009) and Garcia (2010). For missing life history traits, additional information from literature has been considered. The five categories retained are life history functional traits that were selected based on the knowledge of the response of benthic taxa to trawling disturbance (de Juan and Demestre, 2012). They reflect respectively the possibility to avoid direct gear impact, to benefit from trawling for feeding, to escape gear, to get caught by the net and to resist trawling/dredging action, each of these characteristics being either advantageous or sensitive to trawling. Then, to allow quantitative analysis, a score was assigned to each category: from low vulnerability (0) to high vulnerability (3). The five categories scores were then summed for each taxon (the highly vulnerable taxon could reach the maximum score is 15) and this value may be considered as a species index of sensitivity to trawling disturbance. The scores of 812 taxa commonly found in bottom trawl by-catch in the southern North Sea, English Channel and north-western Mediterranean were described.