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REPHYTOX dataset includes long-term time series on phycotoxins in marine bivalve molluscs, since 1987, along the whole French coast. The dataset covers results on lipophilic toxins, PSP toxins, ASP toxins, and palytoxins. REPHYTOX was a full part of the REPHY network until 2015. The whole dataset is available.
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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
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These data are outputs of a spatio-temporal model inferring fish distribution. The maps are based on high-resolution catch data (VMS-logbook). They have a montly time resolution and a 0.05° spatial resolution. Four demersal species of the Bay of Biscay are available in the dataset: common sole (Solea solea), megrim (Lepidorhombus whiffiagonis), anglerfish (Lophius spp) and thornback ray (Raja clavata). Maps are provided for year 2008 to 2018 ; they were produced in the context of the MACCO project (https://www.macco.fr/en/accueil-english/), an Ifremer project that aims at proposing alternative management strategies for the mixed demersal fisheries of the Bay of Biscay.
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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)
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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).
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Diet and stable isotopes of the European eel (Anguilla anguilla L.) in six northern France estuaries
The diet and stable isotopic (i.e. δ15N and δ13C values) compositions of eels have been studied during each season of 2019 with a fyke net in six estuaries located along the French coast of the eastern English Channel (Slack, Wimereux, Liane, Canche, Authie and Somme estuaries) (10.1371/journal.pone.0270348).
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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)
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The Commission for the Conservation Southern Bluefin Tuna collects a variety of data types from its Members and Cooperating Non-Members, including total catch, catch and effort data, and catch at size data. Catch, size and trade information is also collected through the Commission's Catch Documentation Scheme, Japanese import statistics, and other monitoring programs. Annual catches provided on this page are reported on a calendar year basis. CCSBT Members use quota years (not calendar years) for managing catching limits, but quota years differ between Members, so calendar years are used to provide catches on a common timescale. Relevant subsets and summaries of these data are provided below. All figures are subject to change as improved data or estimates become available. In particular, reviews of SBT data in 2006 indicated that southern bluefin tuna catches may have been substantially under-reported over the previous 10-20 years and the data presented here do not include estimates for this unreported catch. Also, data for the last reported year of catch (2020) are preliminary and are subject to revision. Any latitudes and longitudes presented in these summaries represent the north western corner of the relevant grid, which is a 5*5 grid unless otherwise specified. Other information on Members and Cooperating Non-Members fishing activities appears in the reports of the Extended Scientific Committee, Compliance Committee and Extended Commission.
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Data collected by the Spindrift 2 Sails of Change vessel during its attempt at the round-the-world sailing record, the Jules Verne Trophy. More information at https://spindrift-racing.com/fr/.
Catalogue PIGMA