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Bibliographic Details
Main Author: Thomas, Ellen
Format: Dataset Open Access
Language:en
Published: PANGAEA 2003
Subjects:
113-690; Abyssamina poagi; Abyssamina quadrata; AGE; Alabamina creta; Anomalinoides cf. acutus; Anomalinoides rubiginosus; Anomalinoides spissiformis; Aragonia aragonensis; Aragonia sp.; Astacolus spp.; Bolivinita sp.; Bolivinoides cf. decoratus; Bolivinoides decoratus; Bolivinoides delicatulus; Bulimina kugleri; Bulimina midwayensis; Bulimina simplex; Bulimina thanetensis; Bulimina trinitatensis; Buliminella beaumonti; Calculated; Cibicides variabilis; Clinapertina subplanispira; COMPCORE; Composite Core; Coryphostoma sp.; Counting; Cyclammina sp.; DEPTH, sediment/rock; Dorothia oxycona; DSDP/ODP/IODP sample designation; Eilohedra weddellensis; Fishers alpha index of diversity; Foraminifera, benthic; Foraminifera, benthic, uniserial; Foraminifera, benthic, uniserial lagenids; Fursenkoina pauciloculata; Fursenkoina tegulata; Gaudryina pyramidata; Globobulimina sp.; Gravellina narivaensis; Gyroidinoides acutus; Gyroidinoides beisseli; Gyroidinoides depressus; Gyroidinoides girardana; Gyroidinoides globosus; Gyroidinoides planulatus; Gyroidinoides soldanii; Gyroidinoides subquadratus; Heronallenia lingulata; Joides Resolution; Leg113; Lenticulina macrodisca; Lenticulina spp.; Lingulina sp.; Loxostomum sp.; Marginulina spp.; Myllostomella fijiensis; Neoflabellina semireticulata; Nonionella robusta; Nonion havanense; Number of species; Nuttallides cf. truempyi; Nuttallides sp.; Nuttallides truempyi; Nuttallides umbonifera; Ocean Drilling Program; ODP; Oridorsalis umbonatus; Pullenia coryelli; Pullenia jarvisi; Pullenia quadriloba; Pullenia quinqueloba; Pyramidina rudita; Quadrimorphina allomorphinoides; Quadrimorphina profunda; Ramulina spinulosa; Rectobulimina carpentierae; Recurvoides sp.; Rhizammina spp.; Rzehakina epigona; Sample code/label; Saracenaria italica; Seabrookia rugosa; Siphogenerinoides brevispinosa; Siphogenerinoides cf. brevispinosa; Siphonodosaria hispidula; Siphonodosaria lepidula; South Atlantic Ocean; Spiroplectammina spectabilis; Stensioeina beccariiformis; Stilostomella aculeata; Tappanina selmensis; Turrilina brevispira; Unilocular taxa
Online Access:https://doi.org/10.1594/PANGAEA.724678
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Table of Contents:
  • A mass extinction of deep-sea benthic foraminifera has been documented globally, coeval with the negative carbon isotope excursion (CIE) at the Paleocene-Eocene boundary, which was probably caused by dissociation of methane hydrate. A detailed record of benthic foraminiferal faunal change over ~30 k.y. across the carbon isotopic excursion at the Ocean Drilling Program Site 690 (Southern Ocean) shows that shortly before the CIE absolute benthic foraminiferal abundance at that site started to increase. 'Doomed species' began to decrease in abundance at the CIE by a few thousand years. After the extinction faunas were dominated by small species, which resemble opportunistic taxa under high-productivity regions in the present oceans. Calcareous nannofossils (primary producers), however, show a transition to more oligotrophic nannofloras exactly where the benthic faunas show the opposite. Plankton and benthos is thus decoupled. Possibly, a larger fraction of food particles reached the seafloor after the CIE, so that food for benthos increased although productivity declined. Enhanced organic preservation might have resulted from low-oxygen conditions caused by oxidation of methane. Alternatively, and speculatively, there was a food-source at the ocean floor. Benthic foraminifera dominating the post-extinction fauna resemble living species that symbiotically use chemosynthetic bacteria at cold seeps. During increased, diffuse methane escape from hydrates, sulfate-reducing bacteria could have produced sulfide used by chemosynthetic bacteria, which in turn were used by the benthic foraminifera, causing extinction by a change in food supply.