Miocene planktonic foraminifera from the eastern equatorial Pacific

Neogene calcareous sediments were recovered at 11 sites along two north-south transects in the eastern equatorial Pacific Ocean during Ocean Drilling Program (ODP) Leg 138. An overview of planktonic foraminifer distribution in these sediments was presented in Mayer, Pisias, Janecek, et al. (1992) based on a preliminary examination of core-catcher samples. In general, the preservation state of the foraminifers is poor throughout most of the sedimentary sequences, making this microfossil group here of much less value for biostratigraphy than other microfossil groups. Pliocene-Pleistocene planktonic foraminifers from several sites have been analyzed in great detail for their oxygen and carbon isotope composition in various high-resolution studies (Farrell et al., this volume; Mix et al., this volume; Ravello et al., this volume; Shackleton et al., this volume). Planktonic foraminiferal datums of biostratigraphic value have been identified in several of these studies. This report presents planktonic foraminiferal distribution in selected Miocene sediments.

Planktonic foraminifera of sediment core MD01-2390

Sea-surface temperature (SST) estimates in the sediment core MD01-2390 based on planktonic foraminiferal species abundances using five different transfer function techniques suggest nearly unchanged or unusually higher temperatures in the tropical southern South China Sea (SCS) during the Last Glacial Maximum (LGM) relative to modern temperatures. These results are in contrast to substantial cooling of 2-5 °C inferred by geochemical (Uk'37, Mg/Ca ratios) and terrestrial proxies from the western tropical Pacific region. Using multivariate statistics we show that the glacial southern SCS harboured unique planktonic foraminiferal assemblages that have no modern analogs. Analyses of faunal variation through the core reveal that planktonic foraminiferal assemblages responded to temperature changes inferred from Mg/Ca data but that this signal is subdued by superimposed variations in the relative abundance of Pulleniatina obliquiloculata and Neogloboquadrina pachyderma (dextral). These species occur in glacial samples at proportions that are not observed in the calibration data set. The glacial high abundance of N. pachyderma (dextral) are interpreted to reflect a seasonal (winter) inflow of cold surface water from the northeast via the Bashi Strait due to the combined effects of an intensified winter monsoon, a southward shift of the polar front and the eastward migration of the Kuroshio Current. In contrast, processes controlling the high relative abundances of P. obliquiloculata during the LGM may be unique to the southern SCS. We propose a scenario involving a stronger (winter) mixing or enhanced upwelling due to an intensified winter monsoon that prevented shallow-dwelling, warm indicators to establish larger populations during the LGM. Our results indicate that a no-analog behaviour of planktonic foraminifera faunas is responsible for the warm glacial conditions in this part of the western Pacific warm pool as implied by foraminiferal transfer functions and that a more significant surface cooling in the region as implied by terrestrial and geochemical (Mg/Ca ratios; alkenone unsaturation index) marine proxies is a more likely scenario.

Planktonic foraminifera stratigraphy and datums of ODP Site 184-1143 and Hole 184-1146A, South China Sea

The biostratigraphy of Miocene-age sediment samples recovered from Ocean Drilling Program Sites 1143 and 1146, South China Sea, is presented. The preservation of the planktonic foraminifers recovered from both sites varies widely, from poor to very good. The volume of biogenic sediment in the >63-µm size fraction also varies considerably, with many samples being dominated by mud. In comparison to shipboard biostratigraphy, based on core catcher analyses with a depth resolution of ~10 m, we analyzed samples from the two stratigraphic columns every 2-3 m (~45- to 93-k.y. resolution). The placement of planktonic foraminifer zonal boundaries was made at a resolution of ~1.5 m at Site 1146 and ~3.0 m at Site 1143. The higher resolution has resulted in significant changes in biostratigraphic zonal boundary locations compared to shipboard results. For the time interval of 5.54-10.49 Ma, the changes in zonation reveal similar age-depth models at both sites, with three segments of changing sedimentation rate through the upper Miocene, though the differences in sedimentation rates at Site 1146 are subtler than those at Site 1143. The boundary between lithologic Units II and III at Site 1146 corresponds to a sharp change in sedimentation rate (58 to 21 m/m.y.) at 15.1 Ma (the first occurrence of Orbulina suturalis). At this site, the interval from 16.4 to 15.1 Ma is characterized by very high mass accumulation rates in the noncarbonate fraction. Above this interval the carbonate fraction becomes increasingly important in the sediment flux to the South China Sea. At Site 1143, sedimentation rates increase from 8 to 99 m/m.y. at 8.6 Ma. This corresponds to a dramatic increase in both carbonate and noncarbonate mass accumulation rates at the site, but no change in lithology.

Nannofossil and planktic foraminiferal events of ODP Site 166-1006 sediments

Detailed biostratigraphy in Site 1006 based on planktonic foraminifers and nannofossils shows large-scale sedimentation rate variability in the Florida Strait west of the Great Bahama Bank. A 'floating' cyclostratigraphy based mainly on resistivity logs and magnetic susceptibility data has been fixed to the biostratigraphy in the absence of magnetostratigraphy. The strongest orbital cycle present is the precessional beat, which is present in the borehole logs throughout the record. Counting the cycles resulted in an accurate time scale and thus a sedimentation rate time series. Spectral analysis of the sedimentation rate time series shows that the short-term cycle of eccentricity (~125 k.y.) and the long term cycle of eccentricity (~400 k.y.) are pervasive throughout the Miocene record, together with the long-term ~2-m.y. eccentricity cycle. The Great Bahama Bank produced pulses of shallow carbonate input once every precessional (sea level) cycle during the Miocene and perhaps two pulses per cycle in the early Pliocene. The amount of sediment exported in these pulses appears to be controlled by eccentricity modulation of the precessional amplitude and therefore the amplitude of the sea-level rise. Finally, an increase in sedimentation rate just after the Miocene/Pliocene boundary is attributed to a change in the location and strength of sediment drift currents in the Florida Strait due to reorganization of the currents following the closure of the Panama Isthmus.

Occurrence and estimated abundance of planktonic foraminifers at DSDP Leg 85 holes

Tropical planktonic foraminifers occur throughout the sequences at all sites of Leg 85, and the standard planktonic foraminiferal zonation of Blow (1969) is applicable to most of the recovered sequences. However, the abundance and state of preservation of foraminifers decline markedly in certain intervals because of the effects of dissolution. Although siliceous microfossils studied on this leg indicate recovery of nearly complete records for the Pleistocene to Oligocene interval, the planktonic foraminiferal biostratigraphy is interrupted by strongly dissolved sections at all sites. Particularly, faunas assignable to Zone N7 (early Miocene) and Zone N15-16 (early late Miocene) are almost totally unrecognizable throughout the eastern equatorial Pacific. Well-preserved and diverse planktonic foraminifers occur in the lower middle Miocene, where the evolutionary developments of Orbulina universa d'Orbigny and Globorotalia fohsi Cushman and Ellisor are well represented. The Orbulina first appearance datum is observed to be nearly coincident with the last occurrence level of the diatom Annellus californicus Tempère, thus .establishing an age of 15 Ma for this datum by using the paleomagnetic calibration of the diatom datum. Moderately well-preserved late Eocene planktonic foraminifers occur in the carbonate sediments immediately overlying the basalt basement at Sites 573 and 574. The Eocene-Oligocene faunal transition, however, is masked at both sites by an intercalation of metalliferous layers containing no planktonic foraminifers.