Composition and age of bottom sediments from the Southern Ocean

Geomorphology, geology, stratigraphy, lithology and geochemistry of bottom sediments in the South Ocean are under consideration. Regularities of distribution of iron-manganese nodules, features of occurrence of ore components in the nodules, nodule abundance in bottom sediments have been studied.

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.

Benthic foraminifera of ODP Leg 116 holes

Benthic foraminifers were examined from turbiditic sequences at Sites 717, 718, and 719. Three assemblages, 1, 2, 3, were identified and are interpreted as reflecting different bathymetric environments. Based on the distribution patterns of these assemblages, six paleontological intervals (a to f) were distinguished and correlated to the lithostratigraphic units and calcareous nannofossil biostratigraphy and biochronology. This relationship indicated three signals of climatic deterioration, the first in the late Pliocene (around 2.42 Ma) and two others in the Pleistocene (younger than 1.59 Ma and 0.93 Ma).

Benthic foraminifera and stable isotope record of ODP Leg 182 sites

Cores from Sites 1129, 1131, and 1132 (Ocean Drilling Program (ODP) Leg 182) on the uppermost slope at the edge of the continental shelf in the Great Australian Bight reveal the existence of upper Pleistocene bryozoan reef mounds, previously only detected on seismic lines. Benthic foraminiferal oxygen isotope data for the last 450,000 years indicate that bryozoan reef mounds predominantly accumulated during periods of lower sea level and colder climate since stage 8 at Sites 1129 and 1132 and since stage 4 at the deeper Site 1131. During glacials and interstadials (stages 2-8) the combination of lowered sea level, increased upwelling, and absence of the Leeuwin Current probably led to an enhanced carbon flux at the seafloor that favored prolific bryozoan growth and mound formation at Site 1132. At Site 1129, higher temperatures and downwelling appear to have inhibited the full development of bryozoan mounds during stages 2-4. During that time, favorable hydrographic conditions for the growth of bryozoan mounds shifted downslope from Site 1129 to Site 1131. Superimposed on these glacial-interglacial fluctuations is a distinct long-term paleoceanographic change. Prior to stage 8, benthic foraminiferal assemblages indicate low carbon flux to the seafloor, and bryozoan mounds, although present closer inshore, did not accumulate significantly at Sites 1129 and 1132, even during glacials. Our results show that the interplay of sea level change (eustatic and local, linked to platform progradation), glacial-interglacial carbon flux fluctuations (linked to local hydrographic variations), and possibly long-term climatic change strongly influenced the evolution of the Great Australian Bight carbonate margin during the late Pleistocene.

Upper Cretaceous agglutinated foraminifers from the western Pacific Ocean

Abyssal agglutinated foraminifers allow biostratigraphic correlation of Upper Cretaceous brown zeolitic claystones in Deep Sea Drilling Project Holes 196A and 198A and Ocean Drilling Program Holes 800A and 801 A. Three agglutinated foraminiferal zones subdivide the strata overlying the Campanian to Cenomanian cherts. The lower zone is characterized by Hormosina gigantea, which is a Campanian zonal marker in the North Atlantic Ocean and western Tethys. A major correlation level, which was observed in all holes studied, is based on the acme of evolute Haplophragmoides spp. This acme zone was observed in Sample 129-801A-6R-CC, about 9 m above the first occurrence of H. gigantea in Sample 129-801A-7R-1, 62-67 cm (approximately middle Campanian). The uppermost zone is characterized by dominant Paratrochamminoides spp. and in some instances common Bolivinopsis parvissimus (late Campanian to Maestrichtian). The available biostratigraphic data for the Upper Cretaceous of Sites 196, 198, 800, and 801 are correlated with the biochronologic framework of the North Atlantic, western Mediterranean, and Carpathians. Additionally, we use quantitative estimates of the diversity and abundance of agglutinated foraminiferal species to monitor general faunal trends with time in the western Pacific.