The Argo program provides an unprecedented volume of oceanographic data, yet the complexity of its dataset — involving multiple data modes, quality control flags, and metadata conventions — often hinders its direct usage. The EasyOneArgo initiative addresses this challenge by delivering simplified, high-quality subsets of Argo data, specifically designed to streamline user access and integration. The EasyOneArgo data product is comprised of 4 datasets: - EasyOneArgoTS – A curated selection of temperature-salinity profiles filtered by strict quality criteria and optimized across raw, real-time adjusted, and delayed-mode status. - EasyOneArgoTSLite – The vertically interpolated counterpart of EasyOneArgoTS, with standardized pressure levels between 2 and 6000 dbar. - EasyOneArgoBGC – A curated selection of biogeochemical profiles filtered by strict quality criteria. The BGC parameters include DOXY, NITRATE, PH, CHLA, BBP, and various radiometry parameters. All BGC data are adjusted either in real-time or in delayed-mode. Accompanying TS measurements are also included. - EasyOneArgoBGCLite – The vertically interpolated counterpart of EasyOneArgoBGC, with the same standardized pressure levels as EasyOneArgoTSLite. Note: The BGC vertical interpolation process involves pre-filtering the original data before interpolation. Hence the magnitudes of some of the features are modulated in the BGCLite dataset. Each profile in EasyOneArgo is packaged as a standalone CSV file, with metadata and indexes for seamless retrieval. This work represents a user-centric shift in Argo data delivery: no QC flags, no data modes, no data manuals — just good, clean, structured ocean data ready for immediate scientific application. The EasyOneArgo data product is publicly available through monthly FAIR-compliant releases. We invite community feedback for continued refinement. Please send any comments to Annie Wong (apsw.uw@gmail.com) or Thierry Carval (Thierry.Carval@ifremer.fr).

Three saltmarshes, Aiguillon, Brouage, Fier d'Ars, located in the Pertuis-Charentais Sea along the south-west coast of France, were studied to evaluate their sediment and mass accumulation rates (SAR; MAR) based on 210Pb and 137Cs profiles in sediments. Coastal saltmarshes play indeed an essential role in providing services such as coastal protection and supporting biodiversity. Saltmarshes are also critical environments for the accumulation of sedimentary organic carbon (blue carbon). However, the number of studies on saltmarshes remains underrepresented compared to studies on mangroves and seagrass. This work is a contribution to the effort to document sediment and mass accumulation rates of saltmarshes.A total of 16 1m sediment cores were collected in the three saltmarshes (Aiguillon, Brouage, Fier d'Ars) in 2021 and 2022 using an Eijkelkamp stainless steel peat sampler. Each sediment core was sampled 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 (210Pb, 226Ra, 137Cs, 228Th, 137Cs). Combining excess 210Pb and 137Cs has allowed to establish a reliable chronology of sediment deposition on a multidecadal timescale.

The dataset dcm_dtb.txt contains bio-optical measurements and environmental parameters associated with  Deep Chlorophyll Maxima (DCM) acquired by BGC-Argo profiling floats. For each BGC-Argo profile the data files includes the World Meteorological Organization (WMO) and profile numbers, the Data Assembly Center (DAC), the geographical position (LON and LAT), the date of the profile in Julian Day (JULD) and in YYYY-MM-DD format; the region of the profile (REGION, acronyms detailed in the region.txt file), the DCM zonal attribution (ZONE, acronyms detailed in the zone.txt file), the vertical resolution of measurements of the concentration of the chlorophyll a [Chla] and of the backscattering coefficient (bbp) within the 250 first meters, the Mixed Layer Depth (MLD, m), the qualification of the vertical profile (DCM_TYPE) as Deep Biomass Maximum (3), Deep photoAcclimation Maximum (2), or presenting no DCM (1); the depth of the DCM (DCM_DEPTH); the chlorophyll a concentration (CHLA_DCM, mg chla m-3 ) the backscattering coefficient (BBP_DCM, m-1), and the Brunt-Vaisala frequency (N2_DCM) at the DCM depth; the nitracline depth (NCLINE_DEPTH, m) and steepness (NCLINE_STEEP, µmol NO3 m-3 m-1), the mean nitrate concentration within the Mixed Layer (NO3_MEAN_MLD, µmol NO3 m-3), the mean daily Photosynthetically Available Radiation in the Mixed Layer (MEAN_IPAR_MLD, E m -1 d -1), the daily Photosynthetically Available Radiation at the nitracline depth (IPAR_NCLINE, E m-2 d-1);  and the [Chla] measured by satellite (CHLA_SAT, mg chla m-3). The dataset shape_NASTG_ASEW.txt contains the seasonal median, the first and third quartiles of the [Chla] and of the bbp profiles for the North Atlantic Subtropical Gyre and Atlantic SubEquatorial Waters regions. The dataset climato_NASTG_ASEW.txt contains the monthly mean and standard deviations of the DCM depth (DCM_depth), the isolume depth of daily Photosynthetically Available Radiation of 20 E m-2 d-1 (iPAR_20), the nitracline depth, and the Mixed Layer Depth (MLD) for the profiles within the North Atlantic Subtropical Gyre and Atlantic SubEquatorial Waters regions.  The qualification and processing of the BGC-Argo profiles, as well as the DCM detection (DCM_TYPE) and the estimation of the environmental parameters, were applied as described from Cornec, M., Claustre, H., Mignot, A., Guidi, L., Lacour, L., Poteau, A., D’Ortenzio, F.,Gentili, B., Schmechtig, C., (to be updated.) Deep Chlorophyll Maxima in the global ocean: occurrences, drivers and characteristics. Global Biogeochemical Cycles, to be updated The [Chla] satellite variable was obtained by the match of each BGC-Argo profile with a L3S [Chla] product from the Ocean Colour-Climate Change Initiative v4.0 database merging observations from MERIS, MODIS, VIIRS and SeaWiFs, at a monthly and 4x4-km-pixel resolution, up to December 31, 2019 (ftp://oc-cci-data:ELaiWai8ae@oceancolour.org/occci-v4.2/).

The network was initiated by IFREMER from 1993 to 2009 (under the acronym REMORA) to study the rearing performance of the Pacific oyster Crassostrea gigas at a national scale. To do so, the network monitored annually the mortality and growth of standardized batches of 18-month-old oysters. Starting in 1995, the monitoring of the rearing performance of 6-month-old oyster spat was integrated into this network. These sentinel batches were distributed simultaneously each year on 43 sites and were monitored quarterly. These sites were distributed over the main French oyster farming areas and allowed a national coverage of the multiannual evolution of oyster farming performances. Most of the sites were located on the foreshore at comparable levels of immersion. Field studies were carried out by the "Laboratoires Environnement Ressources" (LER) for the sites included in their geographical area of investigation. Following the increase in spat mortality in 2008, the network evolved in 2009 (under the acronym RESCO). From this date, the network selected 13 sites among the 43 sites previously monitored in order to increase the frequency of visits (twice a month) and the number of sentinel batches. More precisely, sentinel batches of oysters corresponding to different origins (wild or hatchery, diploid or triploid) and to two rearing age classes (spat or 18-month-old adults) were selected. The monitoring of environmental variables (temperature, salinity) associated with the 13 sites was also implemented. The actions of the network have thus contributed to disentangle the biotic and abiotic parameters involved in mortality phenomena, taking into account the different compartments (environment / host / infectious agents) likely to interact with the evolution of oyster rearing performance. Finally, since 2015, the network has merged the RESCO and VELYGER networks to adopt the acronym ECOSCOPA. The general objective of this current network is to analyze the causes of spatio-temporal variability of the main life traits (Larval stage - Recruitment - Reproduction - Growth - Survival - Cytogenetic abnormalities) of the cupped oyster in France and to follow their evolution on the long term in the context of climate change. To do this, the network proposes a regular spatio-temporal monitoring of the major proxies of the life cycle of the oyster, organized in three major thematic groups: (1) proxies related to growth, physiological tolerance and survival of experimental sentinel populations over 3 age classes: (2) proxies related to reproduction, larval phase and recruitment of the species throughout its natural range in France, and: (3) proxies related to environmental parameters essential to the species (weather conditions, temperature, salinity, pH, turbidity, chlorophyll a and phytoplankton) at daily or sub-hourly frequencies. Working in a geographical network associating several laboratories, ECOSCOPA provide these monitoring within 8 sites selected among the previous ones to ensure the continuity of the data acquisition. Today, these 8 sites are considered as ecosystems of common interest, contrasted, namely : - The Thau lagoon - The Arcachon basin - The Marennes Oléron basin - The Bourgneuf Bay - The bay of Vilaine - The bay of Brest - The bay of Mont Saint Michel - The bay of Veys The ECOSCOPA network is therefore one of the relevant monitoring tools on a national scale, allowing to objectively measure through different proxies the general state of health of cultivated and wild oyster populations, and this for the different sensitive phases of their life cycle. This network aims at allowing a better evaluation, on the long term, of the biological risks incurred by the sector but also by the ecosystems, in particular under the increasing constraint of climatic and anthropic changes. Figure : Sites monitored by the ECOSCOPA network  

LOCEAN has been in charge of analyzing the isotopic composition of the dissolved inorganic carbon (DIC) in sea water collected during a series of cruises or ships of opportunity mostly in the southern Indian Ocean , the North Atlantic, and the equatorial Atlantic, but also in the Mediterranean Sea and in the equatorial Pacific. The LOCEAN sea-water samples for δ13CDIC were collected in 125/25 ml glass bottles until 2022/since then and poisoned with HgCl2 (1 ml of saturated solution) before storage in a dark room à 4°C until their measurement. The DIC was extracted from the seawater by acidification with phosphoric acid (H3PO4 85%) and CO2 gas that was produced was collected in a vacuum system following the procedure described by Kroopnick (1974). The isotopic composition of CO2 was determined using a dual inlet-isotopic ratio mass spectrometer (SIRA9-VG) by comparing the 13C/12C ratio of the sample to the 13C/12C ratio of a reference material, the Vienna-Pee Dee Belemnite (V-PDB). The isotopic composition is expressed in the δ-unit defined by Craig (1957)(method type 2).  Experience showed that samples older than 3-4 years are likely to have experienced conservation issues and have been dismissed. The mass spectrometer has worked very well until 2014-2015. Afterwards, its aging as well as the aging of the preparation line resulted in more data loss, and often less accurate results. The preparation line was renovated in 2019, and analyses in 2020 were run manually, often repeating the measurement a second time for each sample. Up to 2007-2008, δ13CDIC values have a precision of±0.01 ‰ (Vangriesheim et al.,2009) and a reproducibility of±0.02 ‰. After an interlaboratory comparison exercise led by Claire Normandeau (Dalhousie  University),  results  suggest  that  recent  LOCEAN  samples have a slightly poorer reproducibility (±0.04 ‰ ) as well as an offset of -0.13‰ (details available in Reverdin et al., ESSD 2018) that is confirmed by Becker et al. 2016 work by comparison with other cruises after removing the anthropogenic signal. Recent comparisons in early May 2021 with Orsay GEOPS facility samples suggest that the current offset is much smaller and might be +0.03‰. LOCEAN has installed in 2021 a new measurement device by coupling a Picarro G2131-I cavity ring down spectrometer (CRDS) with a CO2 extractor (Apollo SciTech) that will measure at the same time DIC (method type 3) (Leseurre, 2022). Since then, all water samples have been analyzed on this device. Part of the data set, as well as a scientific context and publications are also presented on the WEB site https://www.locean-ipsl.upmc.fr/oceans13c. Individual files correspond to regional subsets of the whole dataset. The file names are based on two letters for the region followed by (-) the cruise or project name (see below) followed by –DICisotopes, followed by either -s (surface data) or -b (subsurface data), and a version number (-V0, …): example SI-OISO-DICisotopes-s-V0; the highest version number corresponds to the latest update of the cruise/project data set, and can be directly downloaded. Earlier versions can be obtained on request, but are not recommended. The region two letters are the followings:   - SI: station and surface data in the Southern Indian Ocean that include cruises : INDIGO I (1985 – stn) (https://doi.org/10.17600/85000111) CIVA I (1993 – stn & surf) (https://doi.org/10.17600/93000870) (Archambeau et al., JMS 1998) ANTARES (1993 – stn & surf) (https://doi.org/10.17600/93000600) OISO (*) (since 1998 – stn & surf) (https://doi.org/10.18142/228) (Racapé et al., Tellus 2010, Leseurre, 2022)   - EA: station and surface data in the Tropical Atlantic Ocean that include cruises : EQUALANT (1999 & 2000 – surf) (https://doi.org/10.18142/98) EGEE (2005 to 2007 – stn & surf) (https://doi.org/10.18142/95) PIRATA (since 2013 – stn & surf) (https://doi.org/10.18142/14) EUMELI 2 (1991 – stn) (https://doi.org/10.17600/91004011)  (Pierre et al., JMS 1994) BIOZAIRE 3 (2003 – stn & surf ) (https://doi.org/10.17600/3010120) (Vangriesheim et al., DSRII, 2009) TARA-Microbiomes (2021 - stn & surf)   - NA : station and surface data in the North Atlantic Subpolar gyre that include cruises : OVIDE (**) (since 2002 – stn & surf) (https://doi.org/10.17882/46448) (Racapé et al., 2013) RREX (2017 – stn & surf) (https://doi.org/10.17600/17001400) SURATLANT (since 2010 - surf) (https://doi.org/10.17882/54517) (Racapé et al., BG 2014 ; Reverdin et al., ESSD 2018, Leseurre, 2022) NUKATUKUMA (since 2017- surf)   - MS: station data in the Mediterranean sea that include cruises : ALMOFRONT 1 (1991 – stn) (https://doi.org/10.17600/91004211) VICOMED 3 (1990 – stn) (https://doi.org/10.17600/90000711)   - PO: tropical Pacific that include cruises : PANDORA (2012 – stn) (https://doi.org/10.17600/12010050) ALIZE2 (1991 – stn & surf) (https://doi.org/10.17600/91002711) (Laube-Lenfant and Pierre, Oceanologica Acta 1994)   - SO: station and surface data in the Southern Ocean (except OISO) that include cruises: TARA-Microbiomes (2021-2022, stn & surf) AGULHASII-072022 (2022, stn) CONFLUENCE (1993-1994, stn)   - AO: station and surface data in the Arctic Ocean and nearby seas that include cruises: GREENFEEDBACK (2024, stn&surf) TCA (2024, stn) REFUGE ARCTIC (2024, stn) (*) The values for cruises OISO19, 21 and 22 are doubtful (for some, too low) and will require further investigation to find whether adjusted values can be proposed. (**) Some of the OVIDE cruises are also referred to as or GEOVIDE (in 2014), and BOCATS (in 2016). CATARINA, BOCATS1 and BOCATS2 (PID2019-104279GB-C21/AEI/10.13039/501100011033) cruises were funded by the Spanish Research Agency  The values of the OVIDE 2010 stations are doubtful (too low), but no particular error was found, and they have been left in the files.   Data The files are in csv format reported as: - Cruise name, station id, (bottle number), day, month, year, hour, minute, longitude, latitude, pressure (db), depth (m), temperature (°C), temperature qc, salinity (pss-78), salinity qc, d13CDIC, d13CDIC qc, method type - Temperature is an in situ temperature - Salinity is a practical salinity - Method type (1) acid CO2 extraction from helium stripping technique coupled to mass spectrometer, (2) acid CO2 extraction in a vacuum system coupled to mass spectrometer,(3) CO2 extractor (Apollo SciTech) coupled to CRDS measurements. Temperature qc, salinity qc, d13CDIC qc are quality indices equal to: - 0 no quality check (but presumably good data) - 1 probably good data - 2 good data - 3 probably bad data - 4 certainly bad data - 9 missing data (and the missing data are reported with an unlikely missing value)

Worldwide, shellfish aquaculture and fisheries in coastal ecosystems represent crucial activities for human feeding. But these biological productions are under the pressure of climate variability and global change. Anticipating the biological processes affected by climate hazards remains a vital objective for species conservation strategies and human activities that rely on. Within marine species, filter feeders like oysters are real key species in coastal ecosystems due to their economic and societal value (fishing and aquaculture) but also due to their ecological importance. Indeed oysters populations in good health play the role of ecosystem engineers that can give many ecosystem services at several scales: building reef habitats that contribute to biodiversity, benthic-pelagic coupling and phytoplankton bloom control through water filtration, living shorelines against coastal erosion… The Pacific oyster, Crassostrea gigas (Thunberg, 1793), which is currently widespread worldwide, was introduced into the Atlantic European coasts at the end of the 19th century for shellfish culture purposes and becomes the main marine species farmed in France (around 100 000 tons) despite severe mortalities crisis. But in the same time and because of warming, natural oysters beds has spread significantly along the French coast and are supposed to have reach approximately 500 000 tons. In that context, Pacific oyster populations (natural and cultivated) in France are the subjects of many scientific projects. Among them, a specific long-term biological monitoring focuses on the reproduction of these populations at a national scale: the VELYGER national program. With more than 8 years of weekly data at many stations in France, this field-monitoring program offers a valuable dataset for studying processes underpinning reproduction cycle of this key-species in relation to environmental parameters, water quality and climate change.   Database content: Larval concentration (number of individuals per 1.5 m3) monitored, since 2008, at several stations in six bays of the French coast (from south to north): Thau Lagoon and bays of Arcachon, Marennes Oléron, Bourgneuf, Vilaine and Brest (see map below).   Methods used to monitor larval concentration: An important volume of seawater (1.5 m3) is pumped twice a week throughout the spawning season (june-september), at one meter below the surface at high tide (+/- 2h) in several sites within each VELYGER ecosystem. Water is filtered trough plankton net fitted with 40 µm mesh. After a proper rinsing of the net, the retained material is transferred into a polyethylene bottle (1 liter) and fixed with alcohol. At laboratory, sample is then gently filtered and rinse again and transferred into eprouvette. Two sub-samples of 1 mL are then taken using a pipette and examined on a graticule slide for microscope. The microscopic examination is made with a conventional binocular optical microscope with micrometer stage at a magnification of 10 X (or above). During the counting, a special care is necessary as larvae of other bivalves are also collected and confusion is possible. Larvae of C. gigas are also classified into four stage of development: - Stage I = D-shaped straight hinge larvae (shell length <105 µm) - Stage II = Early umbo evolved larvae (shell length between 105 and 150 µm) - Stage III = Medium umbo larvae (shell length between 150 and 235 µm) - Stage IV*= Large umbo eyed pediveliger larvae (shell length > 235 µm) * Larvae that are very closed to settle are sometimes identified into a separated 5th stage, but generally this stage is included in stage IV.   Illustrations: Location of the different Velyger sites along the French coast. From south to north: Thau Lagoon and bays of Arcachon, Marennes Oléron, Bourgneuf, Vilaine and Brest.   Legend: Pacific Oyster Larvae (left side) and Natural oyster bed (right side). Photos : © S. Pouvreau/Ifremer

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). 

This dataset gathers isotopic ratios (carbon and nitrogen) and concentrations of both priority (mercury species and polychlorinated biphenyls congeners) and emerging (musks and sunscreens) micropollutants measured in a host-parasite couple (hake Merluccius merluccius muscle and in its parasite Anisakis sp) from the south of Bay of Biscay in 2018. In addition, the hake infection degree measured as the number of Anisakis sp. larvae was added for each hake collected.

This dataset contains bio-optical measurements and environmental parameters associated with  Deep Chlorophyll Maxima acquired by BGC-Argo profiling floats and matched with mesoscale eddies location from the Ocean Eddy Detection and Tracking Algorithms (TOEeddies) Atlas. For each BGC-Argo profile the data files includes the World Meteorological Organistion (WMO) and profile numbers, geographical position (LON and LAT), the date of the profile in Julian Day (JULD); the qualification of the vertical profile (CARAC_BIO) as Deep Biomass Maximum (DBM), Deep photoAcclimation Maximum (DAM), or presenting no DCM (NO); at the depth of the maximum (DCM_DEPTH), the chlorophyll a concentration (CHLA_DCM, mg chla m-3 ) and the backscattering coefficient (BBP_DCM, m-1); the Mixed Layer Depth (MLD, m), the nitracline depth (NCLINE, m), the mean daily Available PAR in the Mixed Layer Depth (MIPAR_MLD, E m -1 d -1), the daily Available PAR at the nitracline depth (IPAR_NCLINE, E m-2 d-1); the location of the profile (CARAC_EDDY) as being inside the core/periphery (IN/_EN) of a cyclonic/anticyclonic eddy (DEP_/P_), or outside eddy influence (OUT); the processing level (MODE) of the ADT maps used for the TOEddies detection, either Near Real Time (-1), or Delayed Mode (1). The qualification and processing of the BGC-Argo profiles, as well as the DCM detection (DAM/DBM/NO) and the estimation of the environmental parameters, were applied as described from Cornec, M., Claustre, H., Mignot, A., Guidi, L., Lacour, L., Poteau, A., D'Ortenzio, F., Gentili, B., Schmechtig, C.  (2021). Deep chlorophyll maxima in the global ocean: Occurrences, drivers and characteristics. Global Biogeochem Cycles 35. https://doi.org/10.1029/2020GB006759 Data relative to mesoscale eddies were produced by processing daily 0.25°x0.25° AVISO Absolute Dynamical Topography (maps produced by Ssalto/Duacs and distributed by Copernicus-Marine Environment Services) with the TOEddies algorithm (Laxenaire, R., Speich, S., Blanke, B., Chaigneau, A., Pegliasco, C., & Stegner, A. (2018). Anticyclonic Eddies Connecting the Western Boundaries of Indian and Atlantic Oceans. Journal of Geophysical Research: Oceans, 123(11), 7651–7677. https://doi.org/10.1029/2018JC014270)