Distribution of planktonic foraminifera and other biogenic components in ODP Hole 113-693A (Figure 2)

A planktonic foraminiferal fauna of probable late Aptian age is recorded in Cores 113-693A-47R and -48R, located on the Antarctic continental margin. Moderate to highly productive surface waters and upper bathyal paleodepths are inferred from benthic and planktonic foraminifers, and other biotic and mineral components in the >63 µm size fraction.

Data on multidisciplinary research in the Tajura Rift (Gulf of Aden) during Cruise 7 of R/V Akademik Mstislav Keldysh in winter 1983-1984

In the collective monograph results of geological and geophysical studies in the Tadjura Rift carried out by conventional outboard instruments and from deep/sea manned submersibles "Pisces" in winter 1983-1984 are reported. Main features of rift tectonics, geology, petrology, and geochemistry of basalts from the rift are under consideration. An emphasis is made on lithology, stratigraphy, and geochemistry of bottom sediments. Roles of terrigenous, edafogenic, biogenic, and hydrothermal components in formation of bottom sediments from the rift zone are shown.

Consolidation tests of ODP Leg 113 samples

Examination of the geotechnical characteristics of Weddell Sea, Maud Rise, and South Orkney microcontinental margin sediments recovered during ODP Leg 113 reveals that the reduction in porosity (consolidation) of the siliciclastic, calcareous, and diatomaceous sediments is primarily a process governed by vertical stresses created by overburden. The initial porosity of the sediments in these areas is governed by the amount of diatoms present. The more diatoms, the higher the porosity. Surficial diatom-rich sediments are everywhere overconsolidated. This is attributed to the strong microfabric created by the diatoms, calcareous and clay particles. The deeper diatom-free sediments of Maud Rise range from slightly underconsolidated to normally consolidated. The silty clays and clays of the Weddell Sea and South Orkney margin are underconsolidated. The degree of underconsolidation of these sediments is similar to that determined in a number of different locations throughout the world's oceans. The very low permeability of the Weddell Sea and South Orkney margin sediments appears to account for this underconsolidation.

Oligocene to middle Miocene radiolarians of Maud Rise, Weddell Sea

At Sites 689 and 690, drilled during ODP (Ocean Drilling Program) Leg 113 on the Maud Rise (southeast Weddell Sea), moderately to well preserved radiolarian assemblages were obtained from continuously recovered upper Oligocene and Neogene sequences. Based on radiolarian investigations, a biostratigraphic zonation for a time interval covering the late Oligocene to the middle Miocene is proposed. The radiolarian zonation comprises 10 zones. Five zones are new, and five zones previously defined by Chen (1975) were modified. The zones and the ranges of the nominate species are directly calibrated with a geomagnetic polarity record. This is the first attempt at a direct correlation of late Oligocene to middle Miocene radiolarian zones with the geomagnetic time scale. Six hiatuses were delineated in the studied upper Oligocene to middle Miocene sections. One major hiatus, spanning ca. 6 m.y., is between the upper Oligocene and the lower Miocene sequences. Another important hiatus separates the lower and middle Miocene sediments. As a base for the biostratigraphic investigations, a detailed taxonomic study of the recovered radiolarian taxa is achieved. Three new radiolarian species that occur in upper Oligocene and lower Miocene sediments are described (Cycladophora antiqua, Cyrtocapsella robusta, and Velicucullus altus).

Benthic foraminifera and stable isotope composition in Paleocene-Eocene sediments

In the late Paleocene to early Eocene, deep sea benthic foraminifera suffered their only global extinction of the last 75 million years and diversity decreased worldwide by 30-50% in a few thousand years. At Maud Rise (Weddell Sea, Antarctica; Sites 689 and 690, palaeodepths 1100 m and 1900 m) and Walvis Ridge (Southeastern Atlantic, Sites 525 and 527, palaeodepths 1600 m and 3400 m) post-extinction faunas were low-diversity and high-dominance, but the dominant species differed by geographical location. At Maud Rise, post-extinction faunas were dominated by small, biserial and triserial species, while the large, thick-walled, long-lived deep sea species Nuttallides truempyi was absent. At Walvis Ridge, by contrast, they were dominated by long-lived species such as N. truempyi, with common to abundant small abyssaminid species. The faunal dominance patterns at the two locations thus suggest different post-extinction seafloor environments: increased flux of organic matter and possibly decreased oxygen levels at Maud Rise, decreased flux at Walvis Ridge. The species-richness remained very low for about 50 000 years, then gradually increased. The extinction was synchronous with a large, negative, short-term excursion of carbon and oxygen isotopes in planktonic and benthic foraminifera and bulk carbonate. The isotope excursions reached peak negative values in a few thousand years and values returned to pre-excursion levels in about 50 000 years. The carbon isotope excursion was about -2 per mil for benthic foraminifera at Walvis Ridge and Maud Rise, and about -4 per mil for planktonic foraminifera at Maud Rise. At the latter sites vertical gradients thus decreased, possibly at least partially as a result of upwelling. The oxygen isotope excursion was about -1.5 per mil for benthic foraminifera at Walvis Ridge and Maud Rise, -1 per mil for planktonic foraminifera at Maud Rise. The rapid oxygen isotope excursion at a time when polar ice-sheets were absent or insignificant can be explained by an increase in temperature by 4-6°C of high latitude surface waters and deep waters world wide. The deep ocean temperature increase could have been caused by warming of surface waters at high latitudes and continued formation of the deep waters at these locations, or by a switch from dominant formation of deep waters at high latitudes to formation at lower latitudes. Benthic foraminiferal post-extinction biogeographical patterns favour the latter explanation. The short-term carbon isotope excursion occurred in deep and surface waters, and in soil concretions and mammal teeth in the continental record. It is associated with increased CaC03-dissolution over a wide depth range in the oceans, suggesting that a rapid transfer of isotopically light carbon from lithosphere or biosphere into the ocean-atmosphere system may have been involved. The rapidity of the initiation of the excursion (a few thousand years) and its short duration (50 000 years) suggest that such a transfer was probably not caused by changes in the ratio of organic carbon to carbonate deposition or erosion. Transfer of carbon from the terrestrial biosphere was probably not the cause, because it would require a much larger biosphere destruction than at the end of the Cretaceous, in conflict with the fossil record. It is difficult to explain the large shift by rapid emission into the atmosphere of volcanogenic CO2, although huge subaerial plateau basalt eruptions occurred at the time in the northern Atlantic. Probably a complex combination of processes and feedback was involved, including volcanogenic emission of CO2, changing circulation patterns, changing productivity in the oceans and possibly on land, and changes in the relative size of the oceanic and atmospheric carbon reservoirs.

Paleogene planktonic foraminifera from the southern Kerguelen Plateau

An essentially complete Paleogene record was recovered on the Central and Southern Kerguelen plateaus (55°-59°S) in a calcareous biofacies. Recovery deteriorated in the middle Eocene and down to the upper Paleocene because of the presence of interbedded cherts and chalks. The stratigraphic distribution of about 70 taxa of planktonic foraminifers recovered at Sites 747-749 is reported in this paper. Faunas exhibited fairly high diversity (approximately 20-25 species) in the early Eocene, followed by a gradual reduction in diversity in the middle Eocene. A brief incursion of tropical keeled morozovellids occurred near the Paleocene/Eocene boundary, similar to that recorded on the Maud Rise (ODP Sites 689 and 690). The high-latitude Paleogene zonal scheme developed for ODP Leg 113 sites has been adopted (with minor modifications) for the lower Eocene-Oligocene part of the Kerguelen Plateau record. A representative Oligocene (polarity chronozones 7-13) and late Eocene-late middle Eocene (questionably polarity chronozones 16-18) magnetostratigraphic record has allowed the calibration of several biostratigraphic datum levels to the standard Global Polarity Time Scale (GPTS) and established their essential synchrony between low and high latitudes.

Early Cretaceous palynomorphes from ODP Hole 113-692B

Detailed descriptions of in situ ?Valanginian to Albian Antarctic palynofloras are presented from Weddell Sea claystones with high percentages of organic matter ("black shales") and intercalated volcanic ash layers. The claystones were recovered from two sites (ODP Leg 113, Sites 692 and 693) on the continental margin of Dronning Maud Land. Palynological investigations of these Cretaceous sediments revealed a ?Valanginian-Hauterivian age for the Site 692 sediments and an Aptian-Albian age for Site 693. This paper is focused on the palynomorphs of Site 692. Miospores, dinoflagellate cysts, and acritarchs are listed and compared with early Cretaceous microfloras from the Antarctic Peninsula, Australia, and South America. The dinocyst assemblage of Site 692 seems to be very similar in composition to an assemblage from the South Shetlands (?Valanginian-Hauterivian-Barremian). It also agrees well with associations described from early Early Cretaceous sequences from the Perth Basin, southwestern Australia. According to the Australian miospore zonation schemes, the sporomorph flora from Site 692 belongs to the South Australian Foraminisporis wonthaggiensis Zone (early Valanginian to Hauterivian) or the lower part of the dinocyst Muderongia Superzone (Valanginian to Hauterivian).