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  • 1
    Publication Date: 2023-07-11
    Description: The stations were sampled along the French Mediterranean coast in spring (March-April) 2015 onboard the RV Europe. Bottom sediment at 28 stations (11 to 64 m water depth) was sampled using a Reineck box-corer. Three replicates (“a”, “b”, “c”; different box-corer launches) were done at each station. Each box-corer was sub-cored with a 7.4 cm diameter tube. Only the first top centimetre was preserved in 96% ethanol and stained with 2 g/L Rose Bengal. At the laboratory, after minimum two weeks each sample was washed through four sieves of 63, 125, 150, and 500 µm mesh sizes. Living (stained) benthic foraminifera from the 125-150 µm and 150-500 µm were collected under stereomicroscope and preserved in micropaleontological slides. Taxonomical recognition was done to the species level. The presented data in the table indicate the raw densities of foraminifera sorted per sample. The exact volume of sampled sediment was measured for each sample. Some samples were treated with Sodium Polytungstate (SPT) to separate benthic foraminifera from the sediment. The SPT density is indicated for each treated sample.
    Keywords: according to Parent et al., 2018; Adelosina elegans; Adelosina ferussaci; Adelosina longirostra; Adelosina mediterranensis; Adelosina sp.; Agde Ouest; Aléria (Tavignano); Ammodiscus planus; Ammodiscus sp.; Ammoglobigerina globigeriniformis; Ammoglobigerina sp.; Ammolagena clavata; Ammonia beccarii forma beccarii; Ammonia beccarii forma inflata; Ammonia parkinsoniana forma parkinsoniana; Ammonia parkinsoniana forma tepida; Ammonia perlucida; Ammonia sp.; Ammoscalaria pseudospiralis; Ammoscalaria sp.; Ammoscalaria tenuimargo; Amphicoryna scalaris; Amphicoryna sp.; Antibes Nord; Antibes Sud; Astacolus insolitus; Asterigerinata adriatica; Asterigerinata mamilla; Astrononion stelligerum; BCR; Beauduc; Benthic foraminifera; Benthic foraminifera assemblages; Bigenerina nodosaria; Biloculinella irregularis; Biloculinella labiata; Bolivina dilatata; Bolivina pseudoplicata; Bolivina pygmaea; Bolivina sp.; Bolivina spathulata; Bolivina striatula; Bolivina subaenariensis; Bolivina variabilis; Bonifacio; Box corer (Reineck); Buccella granulata; Buccella sp.; Bulimina aculeata forma aculeata; Bulimina aculeata forma elongata; Bulimina aculeata forma gibba; Bulimina costata; Bulimina marginata; Bulimina sp.; Buliminella elegantissima; Calvi (Revellata); Cancris auriculus; Cap Canaille; Cargèse; Carry; Cassidulina carinata; Cassidulina oblonga; Cassidulinoides bradyi; Chilostomella ovoidea; Cibicidella variabilis; Cibicides lobatulus; Cibicides refulgens; Cibicides sp.; Cibicidoides pseudoungerianus; Clavulina cylindrica; Collioure; Core diameter; Cornuspira involvens; Cornuspira sp.; Cornuspiroides striolata; Cribrostomoides jeffreysii; Cribrostomoides sp.; Cribrostomoides subglobosum; Cycloforina sp.; Cycloforina tenuicollis; Date/Time of event; DCE_4-1; DCE_4-1_Agde_Ouest; DCE_4-1_Aleria; DCE_4-1_Antibes_Nord; DCE_4-1_Antibes_Sud; DCE_4-1_Beauduc; DCE_4-1_Bonifacio; DCE_4-1_Calvi; DCE_4-1_Cap_Canaille; DCE_4-1_Cargese; DCE_4-1_Carry; DCE_4-1_Collioure; DCE_4-1_Faraman; DCE_4-1_Figari_Bruzzi; DCE_4-1_Fos; DCE_4-1_Frejus; DCE_4-1_Grau_du_Roi; DCE_4-1_Gruissan; DCE_4-1_Ile_Embiez; DCE_4-1_Ile_Maire; DCE_4-1_Leucate; DCE_4-1_Marseille_Grande_Rade; DCE_4-1_Menton; DCE_4-1_Nice_Ville; DCE_4-1_Pampelonne; DCE_4-1_Porquerolles; DCE_4-1_Santa_Giulia; DCE_4-1_Toulon_Grande_Rade_2; DCE_4-1_Villefranche; Dentalina bradyensis; Dentalina sp.; Dentalina subsoluta; Depth, bottom/max; DEPTH, sediment/rock; Depth, top/min; Deuterammina dublinensis; Deuterammina sp.; Discorbinella bertheloti; Discorbinella sp.; Discorbis sp.; Eggerella scabra; Eggerella sp.; Elevation of event; Elphidium advenum; Elphidium bartletti; Elphidium complanatum; Elphidium crispum; Elphidium gerthi; Elphidium granosum; Elphidium incertum; Elphidium macellum; Elphidium poeyanum forma decipiens; Elphidium sp.; Elphidium williamsoni; Eponides sp.; Europe; Event label; Faraman; Figari Bruzzi; Fissurina lucida; Fissurina orbignyana; Fissurina quadrata; Fissurina sp.; Fissurina staphyllearia; Foraminifera, benthic agglutinated indeterminata; Foraminifera, benthic hyaline, indeterminata; Foraminifera, benthic porcelaneous indeterminata; Foraminiferal abundance; Fos; Fréjus (St Raphael); Fursenkoina acuta; Fursenkoina complanata; Fursenkoina sp.; Gavelinopsis praegeri; Gavelinopsis sp.; Glandulina laevigata; Glandulina ovula; Glandulina sp.; Globobulimina affinis; Globobulimina sp.; Globocassidulina subglobosa; Globulina myristiformis; Glomospira gordialis; Glomospira sp.; Grau du Roi; Gruissan; Guttulina sp.; Gyroidina sp.; Gyroidina umbonata; Hanzawaia boueana; Hanzawaia sp.; Haplophragmoides canariensis; Haplophragmoides sp.; Haynesina germanica; Haynesina sp.; Hoeglundina elegans; Hormosinella cf. distans; Hormosinella guttifera; Hormosinella sp.; Hyalinonetrion gracillimum; Ile Embiez; Ile Maire; Labrospira kosterensis; Labrospira sp.; Lachlanella undulata; Lagena elongata; Lagena hexagona; Lagenammina atlantica; Lagenammina difflugiformis; Lagenammina sp.; Lagena semistriata; Lagena sp.; Lagena striata; Lagena strumosa; Lagena sulcata; Lagnea sp.; Latitude of event; Lenticulina cf. calcar; Lenticulina orbicularis; Lenticulina peregrina; Lenticulina sp.; Lenticulina vortex; Leptohalysis scotti; Leucate; Living compartment; Longitude of event; Marseille Grande Rade; Mediterranean; Mediterranean Sea France; Melonis barleeanus; Melonis sp.; Menton; Method comment; Miliammina fusca; Miliolida; Miliolinella cf. hybrida; Miliolinella dilatata; Miliolinella elongata; Miliolinella semicostata; Miliolinella sp.; Miliolinella subrotunda; Miliolinella webbiana; Neoconorbina sp.; Neoconorbina terquemi; Nice Ville; Nodosaria sp.; Nonion depressulum; Nonionella cf. turgida; Nonionella sp.; Nonionella stella; Nonionella turgida; Nonionoides grateloupii; Nonion scaphum; Nonion sp.; Nouria cf. polymorphinoides; Nouria polymorphinoides; Nummoloculina sp.; Oolina acuticosta; Oolina sp.; Optional event label; Pampelonne; Parafissurina lateralis forma carinata; Patellina corrugata; Peneroplis pertusus; Planorbulina mediterranensis; Polymorphina sp.; Porosononion sp.; Porquerolles; Psammosphaera fusca; Psammosphaera sp.; Pseudobolivina sp.; Pseudoeponides falsobeccarii; Pseudotriloculina cyclostoma; Pyrgo anomala; Pyrgo depressa; Pyrgo elongata; Quinqueloculina aspera; Quinqueloculina bosciana; Quinqueloculina cf. laevigata; Quinqueloculina costata; Quinqueloculina eburnea; Quinqueloculina laevigata; Quinqueloculina lamarckiana; Quinqueloculina parvula; Quinqueloculina pygmaea; Quinqueloculina seminulum; Quinqueloculina seminulum forma longa; Quinqueloculina sp.; Quinqueloculina spp.; Quinqueloculina stalkeri; Quinqueloculina stelligera; Rectuvigerina phlegeri; Recurvoides sp.; Reophax bilocularis; Reophax cf. scorpiurus; Reophax fusiformis; Reophax fusiformis forma calcareus; Reophax micaceus; Reophax nana; Reophax scorpiurus; Reophax sp.; Reophax spp.; Reophax subfusiformis; Replicate; Reussella spinulosa; Robertinoides bradyi; Rosalina bradyi; Rosalina globularis; Rosalina sp.; Rosalina vilardeboana; Rose Bengal-stained; Saidovina karreriana; Sample volume; Santa Giulia; Scutuloris sp.; Sigmavirgulina tortuosa; Sigmoilina grata; Sigmoilina sp.; Sigmoilinita sp.; Siphonaperta agglutinans; Siphonaperta horrida; Siphonaperta sp.; Siphonina reticulata; Siphotextularia concava; Siphotextularia sp.; Size fraction; Spirillina sp.; Spirillina vivipara; Spiroloculina corrugata; Spiroloculina elevata; Spiroloculina excavata; Spiroloculina grateloupi; Spiroloculina sp.; Spiroloculina tenuiseptata; Spiroplectammina earlandi; Stainforthia fusiformis; Stainforthia sp.; Stereomicroscopy; Stomatorbina concentrica; Technitella legumen; Textularia agglutinans; Textularia conica; Textularia porrecta; Textularia sagittula; Textularia sp.; Tortoplectella rhomboidalis; Toulon Grande Rade 2; Tretomphalus concinnus; Trifarina angulosa; Trifarina carinata; Triloculina oblonga; Triloculina plicata; Triloculina sp.; Triloculina tricarinata; Triloculina trigonula; Triloculinella sp.; Tritaxis sp.; Trochammina sp.; Trochamminula sp.; Usbekistania charoides; Uvigerina mediterranea; Uvigerina peregrina; Valvulineria bradyana; Valvulineria minuta; Vertebralina sp.; Villefranche; Webbinella hemisphaerica; Wellmanellinella striata; Wiesnerella auriculata
    Type: Dataset
    Format: text/tab-separated-values, 53592 data points
    Location Call Number Limitation Availability
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  • 2
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    Unknown
    PANGAEA
    In:  Supplement to: Wary, Mélanie; Eynaud, Frédérique; Sabine, Christopher L; Zaragosi, Sebastien; Rossignol, Pascale E; Malaizé, Bruno; Palis, Edouard; Zumaque, Jena; Caulle, Clémence; Penaud, Aurélie; Michel, Elisabeth; Charlier, Karine (2015): Stratification of surface waters during the last glacial millennial climatic events: a key factor in subsurface and deep-water mass dynamics. Climate of the Past, 11(11), 1507-1525, https://doi.org/10.5194/cp-11-1507-2015
    Publication Date: 2023-10-21
    Description: The last glacial period was punctuated by abrupt climatic events with extrema known as Heinrich and Dansgaard-Oeschger events. These millennial events have been the subject of many paleoreconstructions and model experiments in the past decades, but yet the hydrological processes involved remain elusive. In the present work, high-resolution analyses were conducted on the 12-42 ka BP section of core MD99-2281 retrieved southwest of the Faeroe Islands, and combined with analyses conducted in two previous studies (Zumaque et al., 2012; Caulle et al., 2013). Such a multiproxy approach, coupling micropaleontological, geochemical and sedimentological analyses, allows us to track surface, subsurface, and deep hydrological processes occurring during these rapid climatic changes. Records indicate that the coldest episodes of the studied period (Greenland stadials and Heinrich stadials) were characterized by a strong stratification of surface waters. This surface stratification seems to have played a key role in the dynamics of subsurface and deep-water masses. Indeed, periods of high surface stratification are marked by a coupling of subsurface and deep circulations which sharply weaken at the beginning of stadials, while surface conditions progressively deteriorate throughout these cold episodes; conversely, periods of decreasing surface stratification (Greenland interstadials) are characterized by a coupling of surface and deep hydrological processes, with progressively milder surface conditions and gradual intensification of the deep circulation, while the vigor of the subsurface northward Atlantic flow remains constantly high. Our results also reveal different and atypical hydrological signatures during Heinrich stadials (HSs): while HS1 and HS4 exhibit a "usual" scheme with reduced overturning circulation, a relatively active North Atlantic circulation seems to have prevailed during HS2, and HS3 seems to have experienced a re-intensification of this circulation during the middle of the event. Our findings thus bring valuable information to better understand hydrological processes occurring in a key area during the abrupt climatic shifts of the last glacial period.
    Keywords: 63F/NL; AGE; CALYPSO; Calypso Corer; Counting 〈150 µm; Counting 〉150 µm fraction; DEPTH, sediment/rock; Dinoflagellate cyst per volume; Faeroes Bank; Foraminifera, benthic; Foraminifera, planktic; Grain size, Mastersizer S, Malvern Instrument Inc.; Grain size, mean; IMAGES V; Lithic grains; Marion Dufresne (1995); Mass spectrometer Optima Micromass; MD114; MD99-2281; Modern analog technique (MAT); Neogloboquadrina pachyderma sinistral; Neogloboquadrina pachyderma sinistral, δ18O; Percentile 10; Percentile 50; Percentile 90; Ratio; Sea surface salinity, summer; Sea surface salinity, winter; Sea surface temperature, summer; Sea surface temperature, winter; Sub-surface temperature, summer; Sub-surface temperature, winter
    Type: Dataset
    Format: text/tab-separated-values, 4046 data points
    Location Call Number Limitation Availability
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  • 3
    Publication Date: 2024-02-07
    Description: Highlights • All known observations for Area of Particular Environmental Interest 6 presented. • Assess morphology, sediments, nodules, oceanography, biogeochemistry and ecology. • APEI-6 partially representative of nearby exploration areas yet clear differences. • Present scientific synthesis and management implications for Clarion Clipperton Zone. To protect the range of habitats, species, and ecosystem functions in the Clarion Clipperton Zone (CCZ), a region of interest for deep-sea polymetallic nodule mining in the Pacific, nine Areas of Particular Environmental Interest (APEIs) have been designated by the International Seabed Authority (ISA). The APEIs are remote, rarely visited and poorly understood. Here we present and synthesise all available observations made at APEI-6, the most north eastern APEI in the network, and assess its representativity of mining contract areas in the eastern CCZ. The two studied regions of APEI-6 have a variable morphology, typical of the CCZ, with hills, plains and occasional seamounts. The seafloor is predominantly covered by fine-grained sediments, and includes small but abundant polymetallic nodules, as well as exposed bedrock. The oceanographic parameters investigated appear broadly similar across the region although some differences in deep-water mass separation were evident between APEI-6 and some contract areas. Sediment biogeochemistry is broadly similar across the area in the parameters investigated, except for oxygen penetration depth, which reached 〉2 m at the study sites within APEI-6, deeper than that found at UK1 and GSR contract areas. The ecology of study sites in APEI-6 differs from that reported from UK1 and TOML-D contract areas, with differences in community composition of microbes, macrofauna, xenophyophores and metazoan megafauna. Some species were shared between areas although connectivity appears limited. We show that, from the available information, APEI-6 is partially representative of the exploration areas to the south yet is distinctly different in several key characteristics. As a result, additional APEIs may be warranted and caution may need to be taken in relying on the APEI network alone for conservation, with other management activities required to help mitigate the impacts of mining in the CCZ.
    Type: Article , PeerReviewed , info:eu-repo/semantics/article
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