(Table 1) Benthic foraminifera at DSDP Site 72-516

DSDP Site 516 contains a complete middle Eocene to lower Miocene interval with a well-developed Oligocene sequence that is more than 300 m thick. In this paper, the most important and characteristic benthic foraminiferal species from this interval are described and illustrated, and their quantitative and biostratigraphic distribution is given. Middle Eocene benthic assemblages, derived from pelagic intercalations in a partly turbiditic sequence, are low in diversity. Benthic assemblages of fairly high diversity occur in limestones, chalks, and oozes of the upper Eocene to lower Miocene. The consistently high rate of new species appearances at Site 516 during late Eocene and Oligocene contrasted greatly with the very slow rate of change in abyssal faunas at that time; there were no significant faunal changes at the Eocene/Oligocene boundary. The assemblages are dominated by Cibicidoides (mostly C. ungerianus or C. kullenbergi) and Lenticulina. Buliminids were also important during the Eocene and early Oligocene. Faunal comparison with other Atlantic DSDP sites and drill holes in the Gulf of Mexico suggest an approximately mid-bathyal (500-1500 m) depth of deposition during late Eocene and Oligocene.

Benthic foraminiferal denitrification rates and nitrate storage

The discovery that foraminifera are able to use nitrate instead of oxygen as energy source for their metabolism has challenged our understanding of nitrogen cycling in the ocean. It was evident before that only prokaryotes and fungi are able to denitrify. Rate estimates of foraminiferal denitrification were very sparse on a regional scale. Here, we present estimates of benthic foraminiferal denitrification rates from six stations at intermediate water depths in and below the Peruvian oxygen minimum zone (OMZ). Foraminiferal denitrification rates were calculated from abundance and assemblage composition of the total living fauna in both, surface and subsurface sediments, as well as from individual species specific denitrification rates. A comparison with total benthic denitrification rates as inferred by biogeochemical models revealed that benthic foraminifera account for the total denitrification on the shelf between 80 and 250 m water depth. They are still important denitrifiers in the centre of the OMZ around 320 m (29-56% of the benthic denitrification) but play only a minor role at the lower OMZ boundary and below the OMZ between 465 and 700 m (3-7% of total benthic denitrification). Furthermore, foraminiferal denitrification was compared to the total benthic nitrate loss measured during benthic chamber experiments. Foraminiferal denitrification contributes 1 to 50% to the total nitrate loss across a depth transect from 80 to 700 m, respectively. Flux rate estimates ranged from 0.01 to 1.3 mmol m?2 d?1. Furthermore we show that the amount of nitrate stored in living benthic foraminifera (3 to 705 µmol L?1) can be higher by three orders of magnitude as compared to the ambient pore waters in near surface sediments sustaining an important nitrate reservoir in Peruvian OMZ sediments. The substantial contribution of foraminiferal nitrate respiration to total benthic nitrate loss at the Peruvian margin, which is one of the main nitrate sink regions in the world oceans, underpins the importance of previously underestimated role of benthic foraminifera in global biochemical cycles.

Abundance of benthic foraminifera in late Paleocene to eraly Pliocene sediments of DSDP Hole 74-525A on the Walvis Ridge, South Atlantic (Table 1)

Benthic forammifers in the size-fraction greater than 0.073 mm were studied in 88 Paleocene to Pleistocene samples from Deep Sea Drilling Project Site 525 (Hole 525A, Walvis Ridge, eastern south Atlantic). Clustering of the samples on the basis of the 86 most abundant foramimfers (in total, 331 taxa were identified) allowed separating two major assemblage zones: the Paleocene to Eocene interval, and the Oligocene to Pleistocene interval. Each of these, in turn, were subdivided into three minor subzones as follows: lower upper Paleocene (approx. 62.4 to 57 8 Ma); upper upper Paleocene (56.6 to 56 2 Ma), lower and middle Eocene (55.3 to 46 8 Ma); upper Oligocene to middle Miocene (25.3 to 16 Ma), middle Miocene to Pliocene (15.7 to 4.2 Ma), and lower Pleistocene (0.4 to 0.02 Ma), with only minor differences with the previous zone. Some very abundant taxa span most of the column studies (Bolivina huneri, Cassidulina subglobosa, Eponides bradyi, E. weddellensis, Gavelinella micra, Oridorsalis umbonatus, etc.). Several of the faunal breaks recorded coincide with conspicuous minima in the specific diversity curve, thus suggesting that the corresponding turnovers signal the final stages of periods of faunal impoverishment. At least one major bottomwater temperature drop (as derived from delta18O data) is synchronous with a decrease in the forammiferal specific diversity. On the other hand, a specific diversity maximum in the middle Miocene might be associated with a delta13C increase at approx 16 to 12 Ma. Highest foraminiferal abundances (up to 600-800 individuals per gram of dry sediment) occurred in the late Paleocene and in the early Pleistocene, in coincidence with the lowest diversity figures calculated. The magnitude of the most important faunal turnover recorded, between the middle Eocene and the late Oligocene, is magnified in our data set by the large hiatus which separates the middle Eocene from the upper Oligocene sediments. Considerably smaller overturns occurred within the late Paleocene (in coincidence with changes in the specific diversity, absolute abundance of forammiferal tests, and delta13C), and in the middle Miocene (in coincidence with a specific diversity maximum and a delta13C excursion). New reformation on the morphology and the stratigraphic ranges of several species is furnished. For all the taxa recorded the number of occurrences, total number of individuals identified and first and last appearances are listed.