Benthic foraminifera across the Cretaceous/Paleogene boundary in ODP Hole 198-1210A


Autoria(s): Alegret, Laia; Thomas, Ellen
Cobertura

MEDIAN LATITUDE: 32.622772 * MEDIAN LONGITUDE: 163.424270 * SOUTH-BOUND LATITUDE: 32.223530 * WEST-BOUND LONGITUDE: 158.259360 * NORTH-BOUND LATITUDE: 33.820500 * EAST-BOUND LONGITUDE: 178.919000 * DATE/TIME START: 1978-08-23T00:00:00 * DATE/TIME END: 2001-09-24T14:15:00

Data(s)

12/01/2009

Resumo

Deep-sea benthic foraminifera show important but transient assemblage changes at the Cretaceous/Paleogene (K/Pg) boundary, when many biota suffered severe extinction. We quantitatively analyzed benthic foraminiferal assemblages from lower bathyal-upper abyssal (1500-2000 m) northwest Pacific ODP Site 1210 (Shatsky Rise) and compared the results with published data on assemblages at lower bathyal (~ 1500 m) Pacific DSDP Site 465 (Hess Rise) to gain insight in paleoecological and paleoenvironmental changes at that time. At both sites, diversity and heterogeneity rapidly decreased across the K/Pg boundary, then recovered. Species assemblages at both sites show a similar pattern of turnover from the uppermost Maastrichtian into the lowermost Danian: 1) The relative abundance of buliminids (indicative of a generally high food supply) increases towards the uppermost Cretaceous, and peaks rapidly just above the K/Pg boundary, coeval with a peak in benthic foraminiferal accumulation rate (BFAR), a proxy for food supply. 2) A peak in relative abundance of Stensioeina beccariiformis, a cosmopolitan form generally more common at the middle than at the lower bathyal sites, occurs just above the buliminid peak. 3) The relative abundance of Nuttallides truempyi, a more oligotrophic form, decreases at the boundary, then increases above the peak in Stensioeina beccariiformis. The food supply to the deep sea in the Pacific Ocean thus apparently increased rather than decreased in the earliest Danian. The low benthic diversity during a time of high food supply indicates a stressed environment. This stress might have been caused by reorganization of the planktic ecosystem: primary producer niches vacated by the mass extinction of calcifying nannoplankton may have been rapidly (<10 kyr) filled by other, possibly opportunistic, primary producers, leading to delivery of another type of food, and/or irregular food delivery through a succession of opportunistic blooms. The deep-sea benthic foraminiferal data thus are in strong disagreement with the widely accepted hypothesis that the global deep-sea floor became severely food-depleted following the K/Pg extinction due to the mass extinction of primary producers ("Strangelove Ocean Model") or to the collapse of the biotic pump ("Living Ocean Model").

Formato

application/zip, 2 datasets

Identificador

https://doi.pangaea.de/10.1594/PANGAEA.773872

doi:10.1594/PANGAEA.773872

Idioma(s)

en

Publicador

PANGAEA

Direitos

CC-BY: Creative Commons Attribution 3.0 Unported

Access constraints: unrestricted

Fonte

Supplement to: Alegret, Laia; Thomas, Ellen (2009): Food supply to the seafloor in the Pacific Ocean after the Cretaceous/Paleogene boundary event. Marine Micropaleontology, 73(1-2), 105-116, doi:10.1016/j.marmicro.2009.07.005

Palavras-Chave #198-1210A; 62-465A; A. affinis; A. ammonoides; A. aragonensis; A. cf. A. acutus; A. kuhnti; A. latus; A. velascoensis; Adercotryma kuhnti; Age model; Ammodiscus latus; Ammodiscus sp.; Anomalinoides affinis; Anomalinoides ammonoides; Anomalinoides cf. acutus; Anomalinoides sp.; Anomalinoides spp.; Aragonia aragonensis; Aragonia velascoensis; Astacolus spp.; B. beaumonti; B. decoratus; B. huneri; B. kugleri; B. midwayensis; B. paleocenica; B. simplex; B. velascoensis; Bolivina huneri; Bolivina sp.; Bolivinoides decoratus; Bolivinoides sp.; Bulimina kugleri; Bulimina midwayensis; Bulimina paleocenica; Bulimina simplex; Bulimina spp.; Bulimina velascoensis; Buliminella beaumonti; Buliminella sp.; C. cf. amorpha; C. cf. naranjoensis; C. cf. westi; C. howelli; C. hyphalus; C. incrassata; C. trilatera; Calculated; Cibicidoides cf. naranjoensis; Cibicidoides cf. westi; Cibicidoides howelli; Cibicidoides hyphalus; Cibicidoides sp.; Clavulinoides cf. amorpha; Clavulinoides sp.; Clavulinoides trilatera; Coryphostoma incrassata; Coryphostoma spp.; Counting >63 µm fraction; D. crassa; Deep Sea Drilling Project; Depth; Depth, composite revised; DEPTH, sediment/rock; Depth cr; Dorothia crassa; Dorothia spp.; DRILL; Drilling/drill rig; DSDP; Ellipsoglandulina sp.; Ellipsopolymorphina sp.; Eouvigerina sp.; Event; F. tegulata; FAI; Fishers alpha index of diversity; Fissurina spp.; Foram bent; Foraminifera, benthic; Fursenkoina sp.; Fursenkoina tegulata; G. beisseli; G. depressus; G. girardana; G. globosus; G. pyramidata; G. quadratus; Gaudryina pyramidata; Gaudryina spp.; Glandulina sp.; Globorotalites sp.; Globulina spp.; Glomar Challenger; Gyroidinoides beisseli; Gyroidinoides depressus; Gyroidinoides girardana; Gyroidinoides globosus; Gyroidinoides quadratus; Gyroidinoides sp.; H. lingulata; Heronallenia lingulata; Intercore correlation; Joides Resolution; juvenile; L. rotulata; L. velascoensis; Label; Laevidentalina spp.; Lagena spp.; Leg198; Leg62; Lenticulina rotulata; Lenticulina spp.; Lenticulina velascoensis; M. oxycona; Marssonella oxycona; mbsf; N. cretacea; N. florealis; N. havanense; N. ripleyensis; N. robusta; N. truempyi; Neoflabellina sp.; Nonionella cretacea; Nonionella robusta; Nonionella sp.; Nonion havanense; North Pacific/CONT RISE; North Pacific Ocean; Nuttallides spp.; Nuttallides truempyi; Nuttallinella florealis; Nuttallinella ripleyensis; Nuttallinella sp.; O. plummerae; O. umbonatus; O. velascoensis; Ocean Drilling Program; ODP; ODP sample designation; Oridorsalis plummerae; Oridorsalis umbonatus; Osangularia spp.; Osangularia velascoensis; P. acuminata; P. cretacea; P. hillebrandti; P. jarvisi; P. lunata; P. reussi; P. rudita; Paliolatella sp.; Paralabamina hillebrandti; Paralabamina lunata; Paralabamina sp.; Pleurostomella acuminata; Praebulimina reussi; Praebulimina sp.; Pseudopolymorphina sp.; Pullenia cretacea; Pullenia jarvisi; Pullenia sp.; Pyramidina rudita; Pyrulina spp.; Q. pyramidalis; Quadratobuliminella pyramidalis; Quadrimorphina spp.; R. szajnochae; Reussella szajnochae; S. beccariiformis; S. cretacea; S. hispidula; S. spectabilis; Sample code/label; Scheibnerova sp.; Seabrookia cretacea; Sililoculinina sp.; Siphonodosaria hispidula; sp. 1; sp. A; Spiroplectammina spectabilis; Spiroplectammina spp.; Stensioeina beccariiformis; Stilostomella spp.; T. selmensis; Tappanina selmensis; total specimens counted; Uvigerina sp.; V. lenticula; Valvalabamina lenticula; Westerhold et al., 2008
Tipo

Dataset