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  • 1985-1989  (21)
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  • 1
    Keywords: Foraminifera, agglutinated ; Cenozoic ; Atlantic Ocean
    Type of Medium: Book
    Pages: XIII, 262 S
    Series Statement: WHOI 88-3
    Language: English
    Note: Massachusetts Inst. of Technology/WHOI, PhD Thesis, 1988
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    International journal of earth sciences 78 (1989), S. 1121-1140 
    ISSN: 1437-3262
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Description / Table of Contents: Abstract The stratigraphic and biogeographic distribution of more than 170 species of deep-water agglutinated benthic foraminifers (DWAF) from the North Atlantic and adjacent marginal seas has been compared with paleoenvironmental data (e.g. paleobathymetry, oxygenation of the bottom waters, amount of terrigenous input and substrate disturbance). Six general types of assemblages, in which deep water agglutinated taxa occur, are defined from the Turonian to Maastrichtian times: 1. High latitude slope assemblages 2. Low to mid latitude slope assemblages 3. Flysch-type assemblages 4. Deep water limestone assemblages (»Scaglia«-type) 5. Abyssal mixed calcareous-agglutinated assemblages 6. Abyssal purely agglutinated assemblages Latitudinal differences in faunal composition are observed, the most important of which is the lack or extreme paucity of calcareous forms in high latitude assemblages. East-to-west differences appear to be of comparatively minor importance. Most DWAF species occur in all studied regions and are thus considered as cosmopolitan. Biostratigraphic turnovers in the taxonomic content of assemblages are observed in the lowermost Turonian, mid- Campanian and in the upper Maastrichtian to lowermost Paleocene. These datum levels correspond to inter-regional and time-constant paleooceanographic events, which probably also affected the deep-water benthic biota. This allows us to use deep-water agglutinated foraminifers for biostratigraphy in the North Atlantic sequences deposited below CCD and to geographically extend the currently used zonal schemes which have been established in the Carpathian and Alpine areas.
    Abstract: Résumé La répartition stratigraphique et biogéographique de plus de cent soixante dix espèces de foraminifères benthiques agglutinants d'eaux profondes de l'Océan Atlantique Nord et des mers adjacentes a été examinée en fonction des paramètres du paléoenvironnement (paléobathymétrie, oxygénation et dynamique des eaux de fond, apports détritiques terrigènes). Sur une période s'étendant du Turonien au Maestrichtien, six types principaux d'associations, comprenant en tout ou partie des taxons agglutinants profonds, ont été définis: 1. associations de talus en haute latitude 2. associations de talus en basse latitude 3. associations de type flysch 4. associations de calcaires pélagiques (type »Scaglia«) 5. associations abyssales de type mixte avec foraminifères à test calcaire et foraminifères agglutinants 6. associations abyssales uniquement composées d'agglutinants. Des différences latitudinales sont apparues dans la composition faunique: la plus importante réside dans l'absence ou la très grande rareté des formes à test calcaire dans les associations de haute latitude. Des différences en longitude, d'est en ouest, apparaissent comparativement d'importance mineure. La plupart des espèces de foraminifères agglutinants d'eaux profondes se rencontrent dans toutes les régions étudiées et peuvent donc être considérées comme ubiquistes. De nettes coupures biostratigraphiques, fondées sur des renouvellements fauniques, sont décelées au Turonien basal, au Campanien moyen et au passage Meastrichtien supérieur-Paléocène basal. Ces niveaux repères correspondent à des événements paléo-océanographiques isochrones et d'extension supra-régionale, qui ont probablement affecté aussi les formes benthiques d'eaux profondes. Ceci nous incite à utiliser les foraminifères benthiques profonds pour la biostratigraphie des séries Nord-Atlantique déposées sous la CCD et par corrélation nous permet d'étendre géographiquement l'usage de zonations initialement définies dans le domaine alpino-carpathique.
    Notes: Zusammenfassung Die stratigraphische und biogeographische Verbreitung von mehr als 170 Arten sandschaliger benthischer Tiefwasser-Foraminiferen wurde im Nordatlantik und seinen Randmeeren untersucht. Hierbei wurden die in den einzelnen Untersuchungsgebieten unterschiedlichen Paläoenvironment- Bedingungen (Wassertiefe, Sauerstoffverhältnisse am Ozeanboden, detritischer Eintrag und Beeinträchtigung des Substrats durch Strömungs- und Sedimentationsprozesse) zu der jeweiligen taxonomischen Zusammensetzung der agglutinierenden Benthos-Fauna in Beziehung gesetzt. Für den Zeitraum vom Turon bis zum Maastricht ließen sich zwölf charakteristische Vergesellschaftungen agglutinierender Tiefwasser-Foraminiferen unterscheiden, die in sechs Hauptgruppen zusammengefaßt werden können: 1. Kontinentalhang-Vergesellschaftungen hoher Breiten 2. Kontinentalhang-Vergesellschaftungen niedriger bis mittlerer Breiten 3. Flysch-Vergesellschaftungen 4. Vergesellschaftungen pelagischer Kalke (»Scaglia«-Typ) 5. Abyssale gemischt kalkschalige und agglutinierende Benthos-Vergesellschaftungen 6. Abyssale rein agglutinierende Vergesellschaftungen Biogeographische Unterschiede in der Faunenzusammensetzung korrelieren vor allem mit der geographischen Breite, wobei besonders das Fehlen kalkschaliger Elemente in Faunen hoher Breiten auffällt. Ost-West-Unterschiede sind von geringerer Bedeutung, die Mehrzahl der Arten tritt in allen untersuchten Gebieten auf und kann als kosmopolitisch angesehen werden. Faunenschnitte können im basalen Turon, im mittleren Campan und an der Kreide/Tertiär-Grenze beobachtet werden. Diese Zeitabschnitte sind durch überregionale paläoozeanographische Events charakterisiert, die wahrscheinlich auch das Tiefsee-Benthos beeinflußt haben. Dieser Zusammenhang zwischen der Evolution agglutinierender Tiefsee- Foraminiferen und globalen, zeitkonstanten Events ermöglicht eine biostratigraphische Gliederung der Sub-CCD Serien des Nordatlantik mit Hilfe sandschaliger Foraminiferen, die sich weitgehend mit den Zonierungen, die in den Flyschzonen der Karpathen und Alpen entwickelt wurden, korrelieren läßt.
    Type of Medium: Electronic Resource
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  • 3
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    Unknown
    PANGAEA
    In:  Supplement to: Kaminski, Michael Anthony; Gradstein, Felix M; Scott, David B; Mackinnon, K D (1989): Neogene benthic foraminifer biostratigraphy and deep-water history of sites 645,646, and 647, Baffin Bay and Labrador Sea. In: Srivastava, SP; Arthur, M; Clement, B; et al. (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 105, 731-756, https://doi.org/10.2973/odp.proc.sr.105.123.1989
    Publication Date: 2024-01-09
    Description: Benthic foraminifers were examined from Neogene sediments of Ocean Drilling Program (ODP) Sites 645, 646, and 647 to determine their biostratigraphy and to place constraints on the paleoceanographic history of Baffin Bay, Eirik Ridge, and the Gloria Drift. At Site 645 in Baffin Bay, a Pleistocene Stetsonia assemblage is similar to the modern Baffin Bay assemblage, but an underlying Epistominella takayanagii assemblage has no modern analog. Miocene assemblages below a barren interval display low diversity and consist mainly of agglutinated species. At Site 646 in the Labrador Sea, benthic faunal turnovers occur near important seismic horizons. A Miocene Nuttallides umbonifera assemblage similar to assemblages at other North Atlantic sites occurs below reflector R3. Above reflector R3, a coarse agglutinated assemblage containing more diversified calcareous benthic foraminifers was found that displays affinity to assemblages in the Norwegian-Greenland Sea. The faunal turnover near reflector R3 was interpreted as reflecting the onset (or renewal) of significant Denmark Straits Overflow Water at Site 646 at ~7.5 Ma, Agglutinated species disappear between reflector R2 and the base of the sediment drift, indicating a change in deep-water properties that occurred at ~ 4.7 Ma. This turnover ultimately may be linked to the reopening of the Mediterranean. The beginning of drift sedimentation at the Eirik Ridge is dated at --4.5 Ma. Drift formation ceased at ~2.5 Ma, concomitant with the appearance of ice-rafted sediments. Pleistocene assemblages containing Stetsonia horvathi display affinity to deep assemblages in high-latitude ocean basins. Upper Pliocene and Pleistocene benthic assemblages at Site 647 contain N. umbonifera, which indicates a continued influence of corrosive deep water at the Gloria Drift.
    Keywords: 105-645B; 105-646A; 105-646B; 105-647B; Baffin Bay; DRILL; Drilling/drill rig; Joides Resolution; Labrador Sea; Leg105; Ocean Drilling Program; ODP; South Atlantic Ocean
    Type: Dataset
    Format: application/zip, 5 datasets
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  • 4
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    Unknown
    PANGAEA
    In:  Supplement to: Baldauf, Jack G; Clement, Bradford M; Aksu, Ali E; de Vernal, Anne; Firth, John V; Hall, Frank R; Head, Martin J; Jarrard, Richard D; Kaminski, Michael Anthony; Lazarus, David B; Monjanel, Anne-Lise; Berggren, William A; Gradstein, Felix M; Knüttel, Stephen; Mudie, Peta J; Russell, Merlin D Jr (1989): Magnetostratigraphic and biostratigraphic synthesis of Ocean Drilling Program Leg 105: Labrador Sea and Baffin Bay. In: Srivastava, SP; Arthur, M; Clement, B; et al. (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 105, 935-956, https://doi.org/10.2973/odp.proc.sr.105.165.1989
    Publication Date: 2024-01-09
    Description: During Ocean Drilling Program (ODP) Leg 105, three sites (Sites 645 through 647) were drilled in Baffin Bay and the Labrador Sea to examine the tectonic evolution and the climatic and oceanic histories of this region. Biostratigraphic and magnetostratigraphic results vary at each site, while stratigraphic resolution depends on the limited abundance of marker species and the completeness of the paleomagnetic record. Because of the paucity of planktonic microfossils and the poor paleomagnetic record signatures, stratigraphic determinations at Site 645 often rely on defining minimum temporal constraints on specific samples or stratigraphic intervals. The completed stratigraphy indicates that the sedimentary sequence recovered at Site 645 is early Miocene to Holocene in age. The magnetostratigraphy and biostratigraphies are better defined at Sites 646 and 647 in the Labrador Sea. Site 646 generally contains a well-developed magnetostratigraphy and calcareous microfossil biostratigraphy. This biostratigraphy is based on calcareous nannofossils and planktonic foraminifers typical of the North Atlantic Ocean. Siliceous microfossils are also present at Site 646, but they are restricted to upper Pliocene through Holocene sediments. The stratigraphic sequence recovered at Site 646 is late Miocene to Holocene in age. Based primarily on the calcareous nannofossil stratigraphy, the sequence recovered at Site 647 consists of lower Eocene to lower Oligocene, lower Miocene, upper Miocene, and upper Pliocene through Holocene sediments. Three hiatuses are present in this sequence: the older hiatus separates lower Oligocene sediments from lower Miocene sediments, another hiatus separates lower Miocene sediments from upper Miocene sediments, and the youngest one separates upper Miocene from upper Pliocene sediments. A magnetostratigraphy is defined for the interval from the Gauss/Matuyama boundary through the Brunhes (Clement et al., this volume). Both planktonic foraminifers and siliceous microfossils have restricted occurrences. Planktonic foraminifers occur in Pliocene and younger sediments, and siliceous microfossils are present in lower Miocene and lower Oligocene sediments. The near-continuous Eocene through lower Oligocene sequence recovered at Site 647 allows the calcareous nannofossils and diatom stratigraphies at this site to act as a Paleogene stratigraphic framework. This framework can be compared with the stratigraphy previously completed for DSDP Site 112.
    Keywords: 105-646; 105-647; 12-112; COMPCORE; Composite Core; Deep Sea Drilling Project; DRILL; Drilling/drill rig; DSDP; Glomar Challenger; Joides Resolution; Labrador Sea; Leg105; Leg12; North Atlantic; Ocean Drilling Program; ODP; South Atlantic Ocean
    Type: Dataset
    Format: application/zip, 3 datasets
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  • 5
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    Unknown
    PANGAEA
    In:  Supplement to: Kuhnt, Wolfgang; Kaminski, Michael Anthony; Moullade, Michel (1989): Late Cretaceous deep-water agglutinated foraminiferal assemblages from the North Atlantic and its marginal seas. Geologische Rundschau, 78(3), 1121-1140, https://doi.org/10.1007/BF01829336
    Publication Date: 2024-01-09
    Description: The stratigraphic and biogeographic distribution of more than 170 species of deep-water agglutinated benthic foraminifers (DWAF) from the North Atlantic and adjacent marginal seas has been compared with paleoenvironmental data (e.g. paleobathymetry, oxygenation of the bottom waters, amount of terrigenous input and substrate disturbance). Six general types of assemblages, in which deep water agglutinated taxa occur, are defined from the Turonian to Maastrichtian times: 1. High latitude slope assemblages 2. Low to mid latitude slope assemblages 3. Flysch-type assemblages 4. Deep water limestone assemblages (,,Scaglia,,-type) 5. Abyssal mixed calcareous-agglutinated assemblages 6. Abyssal purely agglutinated assemblages Latitudinal differences in faunal composition are observed, the most important of which is the lack or extreme paucity of calcareous forms in high latitude assemblages. East-to-west differences appear to be of comparatively minor importance. Most DWAF species occur in all studied regions and are thus considered as cosmopolitan. Biostratigraphic turnovers in the taxonomic content of assemblages are observed in the lowermost Turonian, mid-Campanian and in the upper Maastrichtian to lowermost Paleocene. These datum levels correspond to inter-regional and time-constant paleooceanographic events, which probably also affected the deep-water benthic biota. This allows us to use deep-water agglutinated foraminifers for biostratigraphy in the North Atlantic sequences deposited below CCD and to geographically extend the currently used zonal schemes which have been established in the Carpathian and Alpine areas.
    Keywords: 103-641A; 14-137; 14-141; 41-367; 41-368; 78-543A; 93-603B; Ammobaculites agglutinans; Ammobaculites aubertae; Ammobaculites jarvisi; Ammobaculites sp.; Ammodiscus asperellus; Ammodiscus cf. pennyi; Ammodiscus cretaceus; Ammodiscus glabratus; Ammodiscus infimus; Ammodiscus pennyi; Ammodiscus peruvianus; Ammodiscus planus; Ammodiscus sp.; Ammolagena clavata; Ammosphaeroidina pseudopauciloculata; Arenobulimina dorbignyi; Aschemonella carpathica; Aschemonella ex. gr. A. grandis; Bathysiphon spp.; Bolivinopsis parvissimus; Budashevaella trinitatensis; Clavulinoides aspera; Clavulinoides eggeri; Clavulinoides subparisiensis; Cork Harbour; Cribrostomoides sp.; Cribrostomoides trinitatensis; Deep Sea Drilling Project; Dendrophyra ex. gr. D. exceisa; Dendrophyra latissima; Depth, bottom/max; DEPTH, sediment/rock; Depth, top/min; Dorothia crassa trochoides; Dorothia oxycona; Dorothia retusa; Dorothia sp.; DRILL; Drilling/drill rig; DSDP; Epoch; Event label; Gaudryina ex. gr. G. cretacea; Gaudryina pyramidata; Gaudryina sp.; GIB; Gibralta_arch; Glomar Challenger; Glomospira charoides; Glomospira diffundens; Glomospira gordialis; Glomospira irregularis; Glomospira serpens; Glomospirella gaultina; Glomospirella grzybowskii; Goesella rugosa; Guadiana Estuary; GUB; Gubbio; Haplophragmium problematicus; Haplophragmoides bulloides; Haplophragmoides cf. concavus; Haplophragmoides cf. glabra; Haplophragmoides cf. kirki; Haplophragmoides cf. walteri; Haplophragmoides eggeri; Haplophragmoides ex. gr. H. suborbicularis; Haplophragmoides fraudulentus; Haplophragmoides horridus; Haplophragmoides kirki; Haplophragmoides menitens; Haplophragmoides multicamerus; Haplophragmoides multiformis; Haplophragmoides perexplicatus; Haplophragmoides pseudokirki; Haplophragmoides retroseptus; Haplophragmoides sp.; Hormosina crassa; Hormosina excelsa; Hormosina gigantea; Hormosina ovuloides; Hormosina ovulum; Hormosina trinitatensis; Hormosina velascoensis; Hormosinella distans; Hormosinella sp.; Hyperammina dilatata; Hyperammina elongata; Hyperammina subdiscreta; Indian_Habour; Italy; Joides Resolution; Kalamopsis dubia; Kalamopsis grzybowskii; Karreriella conversa; Karreriella horrida; LAB; Labrador; Labrospira inflata; Labrospira pacifica; Labrospira sp.; Lagenammina sp.; Latitude of event; Leg103; Leg14; Leg41; Leg78; Leg78AB; Leg93; Lituotuba lituiformis; Longitude of event; Matanzia varians; MES; Mesoriff_zone; Moroccan margin; North Atlantic/BASIN; North Atlantic/CONT RISE; North Atlantic/DIAPIR; North Atlantic/HILL; Ocean Drilling Program; ODP; Paratrochamminoides acervulatus; Paratrochamminoides heteromorphus; Paratrochamminoides intricatus; Paratrochamminoides irregularis; Paratrochamminoides semipellucidus; Paratrochamminoides sp.; Paratrochamminoides spp.; PEN; Penibetic_zone; Pertuis Charentais; Phenacophragma elegans; Plectorecurvoides parvus; Plectorecurvoides rotundus; Praecystammina cf. globigeriniformis; Praecystammina globigerinaeformis; Psammosphaera fusca; Psammosphaera scruposa; Pseudobolivina cuneata; Pseudobolivina lagenaria; Pseudobolivina munda; Pseudobolivina sp.; Pseudobolivina spp.; Recurvoides anormis; Recurvoides cf. subturbinatus; Recurvoides deflexiformis; Recurvoides gerochi; Recurvoides spp.; Recurvoides walteri; Reophax aff. dentaliniformis; Reophax cf. subnodulosus; Reophax duplex; Reophax globosus; Reophax pilulifer; Reophax sp.; Reophax subfusiformis; Rhabdammina spp.; Rhizammina cf. algaeformis; Rhizammina grzybowskii; Rhizammina indivisa; Rzehakina epigona; Rzehakina fissistomata; Rzehakina inclusa; Rzehakina minima; Saccammina cf. placenta; Saccammina grzybowskii; Saccammina placenta; Saccammina sphaerica; Saccorhiza ramosa; Sample comment; Scheldt Delta Estuary; Silicosigmoilina perplexa; South Atlantic Ocean; Spain; Sphaerammina gerochi; Spiroplectammina aff. dentata; Spiroplectammina aff. spectabilis; Spiroplectammina cf. israelskyi; Spiroplectammina israelskyi; Spiroplectammina laevis; Spiroplectammina navarroana; Spiroplectammina sp.; Spiroplectammina subhaeringensis; Subreophax guttifer; Subreophax pseudoscalaris; Subreophax scalaris; Subreophax sp.; Subreophax splendidus; Thurammina sp.; Tolypammina sp.; TRIN; Trinidad; Trochammina altiformis; Trochammina bulloidiformis; Trochammina deformis; Trochammina ex gr. T. globigeriniformis; Trochammina gyroidinaeformis; Trochammina sp.; Trochammina spp.; Trochamminoides cf. dubius; Trochamminoides cf. proteus; Trochamminoides dubius; Trochamminoides proteus; Trochamminoides subcoronatus; Turritellella shoneana; Uvigerinammina jankoi; Verneuilina cretacea; Verneuilinoides polystrophus; ZUM; Zumaya_section
    Type: Dataset
    Format: text/tab-separated-values, 878 data points
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  • 6
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    Unknown
    PANGAEA
    In:  Supplement to: Kaminski, Michael Anthony; Gradstein, Felix M; Berggren, William A (1989): Paleogene benthic foraminifer biostratigraphy and paleoecology at Site 647, southern Labrador Sea. In: Srivastava, SP; Arthur, M; Clement, B; et al. (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 105, 705-730, https://doi.org/10.2973/odp.proc.sr.105.124.1989
    Publication Date: 2024-01-09
    Description: Benthic foraminifers were examined from the Paleogene of Ocean Drilling Program (ODP) Site 647 and Deep Sea Drilling Program (DSDP) Site 112 in the southern Labrador Sea. The Paleogene sequence of the deep Labrador Sea can be subdivided into seven assemblages, based on the ranges and relative abundance of characteristic taxa. The first occurrences (FOs) and last occurrences (LOs) of important benthic taxa are calibrated to a standard biochronology, by interpolating from our age model for Site 647. The biostratigraphy of Site 647 is used to improve the age estimates of Site112 cores. Fifteen microfossil events in Site 647 also are found in the sedimentary wedge along the Labrador Margin. A comparison of the probabilistic microfossil sequence from the Labrador Margin with that at Site 647 yields four isochronous benthic foraminifer LOs. Two new species are described from Sites 647 and 112: Hyperammina kenmilleri, Kaminski n.sp., and Ammodiscus nagyi Kaminski n.sp. Significant faunal turnovers are observed at the Ypresian/Lutetian and Eocene/Oligocene boundaries. The Ypresian/Lutetian boundary is characterized by a Glomospira-facies and is attributed to a rise in the CCD (carbonate compensation depth) associated with the NP14 lowstand in sea level. The Eocene/Oligocene boundary is delimited by the LO of Spiroplectammina spectabilis and Reticulophragmium amplectens. The change from an Eocene agglutinated assemblageto a predominantly calcareous assemblage in the early Oligocene took place gradually, over a period of about 4 Ma, but the rate of change accelerated near the boundary. This faunal turnover is attributed to changes in the preservationof agglutinated foraminifers, as delicate species disappeared first. Increasingly poorer preservation of agglutinated foraminifers in the late Eocene to earliest Oligocene reflects the first appearance of cool, nutrient-poor deep water in the southern Labrador Sea. The approximately coeval disappearance of agglutinated assemblages along the Labrador Margin was caused by a regional trend from slope to shelf environments, accentuated by the 'mid'-Oligocene lowstand in sea level.
    Keywords: 105-647; Age, maximum/old; Age, minimum/young; Age model; Ageprofile Datum Description; COMPCORE; Composite Core; DEPTH, sediment/rock; Joides Resolution; Leg105; Ocean Drilling Program; ODP; South Atlantic Ocean
    Type: Dataset
    Format: text/tab-separated-values, 101 data points
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  • 7
    Publication Date: 2024-01-09
    Keywords: 105-647A; Catapsydrax dissimilis; Catapsydrax parvulus; Catapsydrax unicavus; DEPTH, sediment/rock; DRILL; Drilling/drill rig; DSDP/ODP/IODP sample designation; Foraminifera, planktic abundance; Globigerina bulloides; Globigerina praebulloides; Globigerina quinqueloba; Globigerinella aequilateralis; Globigerinita glutinata; Globigerinita uvula; Globigerinoides conglobatus; Globigerinoides ruber; Globigerinoides sacculifer; Globorotalia crassaformis; Globorotalia crassula; Globorotalia hirsuta; Globorotalia inflata; Globorotalia menardii; Globorotalia scitula; Globorotalia tosaensis; Globorotalia truncatulinoides; Globorotalia tumida; Joides Resolution; Leg105; Neogloboquadrina atlantica dextral; Neogloboquadrina atlantica sinistral; Neogloboquadrina dutertrei; Neogloboquadrina pachyderma dextral; Neogloboquadrina pachyderma sinistral; Ocean Drilling Program; ODP; Orbulina universa; Pulleniatina obliquiloculata; Sample code/label; South Atlantic Ocean
    Type: Dataset
    Format: text/tab-separated-values, 1980 data points
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  • 8
    Publication Date: 2024-01-09
    Keywords: 105-647A; Aluminium oxide; Barium; Calcium carbonate; Calcium oxide; Cerium; Chromium; Cobalt; Copper; DEPTH, sediment/rock; DRILL; Drilling/drill rig; Gallium; ICP, Inductively coupled plasma; Iron oxide, Fe2O3; Joides Resolution; Lanthanum; Lead; Leg105; Lithium; Loss on ignition; Magnesium oxide; Manganese oxide; Neodymium; Nickel; Niobium; Ocean Drilling Program; ODP; Phosphorus pentoxide; Potassium oxide; Scandium; Silicon dioxide; Sodium oxide; South Atlantic Ocean; Strontium; Thorium; Titanium dioxide; Vanadium; X-ray fluorescence (XRF); Ytterbium; Yttrium; Zinc
    Type: Dataset
    Format: text/tab-separated-values, 4607 data points
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  • 9
    Publication Date: 2024-01-09
    Keywords: 105-646B; Adercotryma glomeratum; Ammobaculites spp.; Ammodiscus spp.; Ammosphaeroidina sp.; Aschemonella spp.; Brizalina spp.; Buccella frigida; Bulimina alazanensis; Cibicidoides bradyi; Cibicidoides lobatulus; Cibicidoides sp.; Cibicidoides spp.; Cyclammina cancellata; Cyclammina pusilla; Dentalina spp.; DEPTH, sediment/rock; DRILL; Drilling/drill rig; DSDP/ODP/IODP sample designation; Eggerella bradyi; Elphidium spp.; Epistominella exigua; Eponides spp.; Fissurina spp.; Foraminifera, benthic; Frondicularia spp.; Fursenkoina fusiformis; Glandulina sp.; Globobulimina auriculata; Globobulimina pacifica; Globocassidulina subglobosa; Glomospira gordialis; Gyroidina orbicularis; Gyroidinoides spp.; Haplophragmoides sp.; Hoeglundina elegans; Islandiella teretis; Joides Resolution; Karreriella bradyi; Karreriella horrida; Labrador Sea; Lagenammina spp.; Lagena spp.; Laticarinina pauperata; Leg105; Lenticulina spp.; Martinottiella spp.; Megafauna, invertebrata, biomass raw; Melonis barleeanus; Melonis pompilioides; Nodosaria pyrula; Nodosaria sp.; Nodosaria spp.; Nonion spp.; Nuttallides umbonifera; Ocean Drilling Program; ODP; Oolina spp.; Ophthalmidium sp.; Oridorsalis umbonatus; Planulina renzi; Planulina wuellerstorfi; Pleurostomella spp.; Polymorphinid species; Psammosphaera fusca; Pseudopolymorphina sp.; Pullenia bulloides; Pullenia subcarinata; Pyrgo murrhina; Quinqueloculina seminulum; Quinqueloculina sp.; Recurvoides spp.; Reophax pilulifer; Rhizammina spp.; Sample code/label; Saracenaria spp.; Sigmoilopsis schlumbergeri; Siphotextularia spp.; Sphaeroidina bulloides; Stilostomella sp.; Tosaia hanzawai; Triloculina arctica; Triloculina trihedra; Trochammina spp.; Trochamminoides sp.; Uvigerina peregrina; Uvigerina sp.
    Type: Dataset
    Format: text/tab-separated-values, 8295 data points
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  • 10
    Publication Date: 2024-01-09
    Keywords: 105-647A; Comment; DEPTH, sediment/rock; DRILL; Drilling/drill rig; DSDP/ODP/IODP sample designation; Iron oxide, Fe2O3; Joides Resolution; Leg105; Manganese oxide; Mineral name; Ocean Drilling Program; ODP; Phosphorus pentoxide; Sample code/label; South Atlantic Ocean; X-ray diffraction (XRD)
    Type: Dataset
    Format: text/tab-separated-values, 54 data points
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