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

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").

(Table 1) Minerals of bulk sediment at DSDP Holes 64-480 and 64-481

This paper provides a brief, descriptive, sedimentological background for the chapters on hydraulic piston core Site 480 in this symposium, and supplements data given in the site chapter for Sites 479-480 (this volume, Pt. 1). Sediments are composed primarily of planktonic diatoms, with minor numbers of silicoflagellates, radiolarians, and varying amounts of both benthic and planktonic foraminifers, along with a large terrigenous component of olive brown, silty clay. The section contains meter-thick intervals of finely laminated facies alternating with nonlaminated zones. A few paleoenvironmental events are documented within the generally uniform sequence by sporadic occurrences of thin turbidites, phosphatic concretions, fish debris concentrations, an ash layer, and a thin layer of diagenetic dolomite. The distribution of nonlaminated and laminated zones is attributed to fluctuations of bottom-water oxygen content caused by variations in circulation, fertility, and productivity. Homogeneous sections are interpreted as coinciding with cooler climatic periods, whereas laminated sections seem to correspond to upwelling conditions during drier periods.

Planktonic foraminifera stratigraphy of ODP Holes 198-1209C and 198-1211C

During Leg 198, the Cretaceous/Paleocene (K/P) boundary was recovered in a remarkable set of cores in nine separate holes at Sites 1209, 1210, 1211, and 1212 on the Southern High of Shatsky Rise. The boundary succession includes an uppermost Maastrichtian white to very pale orange, slightly indurated nannofossil ooze overlain by lowermost Paleocene grayish orange foraminiferal ooze. The boundary between the uppermost Maastrichtian and the lowermost Paleocene is clearly bioturbated. The contact surface is irregular, and pale orange burrows extend 10 cm into the white Maastrichtian ooze. Preliminary investigations conducted on board revealed that the deepest sections of these burrows yielded highly abundant, minute planktonic foraminiferal assemblages dominated by Guembelitria with rare Hedbergella holmdelensis and Hedbergella monmouthensis, possibly attributable to the lowermost Paleocene Zone P0. The substantial thickness of the uppermost Maastrichtian Micula prinsii (CC26) nannofossil Zone and the lowermost Danian Parvularugoglobigerina eugubina (Palpha) foraminiferal Zone suggested that the K/P boundary was rather expanded compared to the majority of deep-sea sites (see Bralower, Premoli Silva, Malone, et al., 2002, doi:10.2973/odp.proc.ir.198.2002). This data report concerns the planktonic foraminiferal biostratigraphy across the K/P boundary in Hole 1209C, the shallowest site (2387 m water depth), and in Hole 1211C, the deepest site (2907 m water depth), where the foraminiferal record across the boundary appeared to be best preserved.

Sediment descriptions, stage, calcium carbonate, organic carbon, delta 13C and geolipids at DSDP Hole 93-603B

Organic matter contents of black shales from the Cretaceous Hatteras and Blake-Bahama formations have been compared to those from surrounding organic-poor strata using C/N ratios, d13C values, and distributions of extractable and nonsolvent-extractable, long-chain hydrocarbons, acids, and alcohols. The proportion of marine and land-derived organic matter varies considerably among all samples, although terrigenous components generally dominate. Most black shales are hydrocarbon-poor relative to their organic-carbon concentrations. Deposition of the black shales in Hole 603B evidently occurred through turbiditic relocation from shallower landward sites and rapid reburial at this outer continental rise location under generally oxygenated bottom-water conditions.