Age and chemical composition of apatites from five DSDP and ODP Sites in the Pacific, Atlantic and Indian Oceans

Since studies on deep-sea cores were carried out in the early 1990s it has been known that ambient temperature may have a marked affect on apatite fission track annealing. Due to sluggish annealing kinetics, this effect cannot be quantified by laboratory annealing experiments. The unknown amount of low-temperature annealing remains one of the main uncertainties for extracting thermal histories from fission track data, particularly for samples which experienced slow cooling in shallow crustal levels. To further elucidate these uncertainties, we studied volcanogenic sediments from five deep-sea drill cores, that were exposed to maximum temperatures between ~10° and 70°C over geological time scales of ~15-120 Ma. Mean track lengths (MTL) and etch pit diameters (Dpar) of all samples were measured, and the chemical composition of each grain analyzed for age and track length measurements was determined by electron microprobe analysis. Thermal histories of the sampled sites were independently reconstructed, based on vitrinite reflectance measurements and/or 1D numerical modelling. These reconstructions were used to test the most widely used annealing models for their ability to predict low-temperature annealing. Our results show that long-term exposure to temperatures below the temperature range of the nominal apatite fission track partial annealing zone results in track shortening ranging between 4 and 11%. Both chlorine content and Dpar values explain the downhole annealing patterns equally well. Low chlorine apatite from one drill core revealed a systematic relation between Si-content and Dpar value. The question whether Si-substitution in apatite has direct and systematic effects on annealing properties however, cannot be addressed by our data. For samples, which remained at temperatures <30°C, and which are low in chlorine, the Laslett et al. [Laslett G., Green P., Duddy I. and Gleadow A. (1987) Thermal annealing of fission tracks in apatite. Chem. Geol. 65, 1-13] annealing model predicts MTL up to 0.6 µm longer than those actually measured, whereas for apatites with intermediate to high chlorine content, which experienced temperatures >30°C, the predictions of the Laslett et al. (1987) model agree with the measured MTL data within error levels. With few exceptions, predictions by the Ketcham et al. [Ketcham R., Donelick R. and Carlson W. (1999) Variability of apatite fission-track annealing kinetics. III: Extrapolation to geological time scales. Am. Mineral. 84/9, 1235-1255] annealing model are consistent with the measured data for samples which remained at temperatures below ~30°C. For samples which experienced maximum temperatures between ~30 and 70°C, and which are rich in chlorine, the Ketcham et al. (1999) model overestimates track annealing.

Composition of ferromanganese crusts from the Atlantic, Pacific and Indian Oceans

A collection of layered ferromanganese ores (27 samples) from the Atlantic and Pacific oceans was studied. Trace element and PGE contents were determined layer-by-layer (up to 10 microlayers) in 13 of these samples. The trace, rare earth, and platinum group element distributions, including their layer-to-layer variations, were compared in hydrogenic and hydrothermal crusts from different regions. It was found that the main PGE variations (by a factor of 10-50) are related to their layer-to-layer variations within a given ore field. The distributions of PGE and trace elements are strongly heterogeneous, which is related, first, to different contents of the elements in the layers of different age in ferromanganese crusts (FMC) and, second, to the observed regional heterogeneity and influence of hydrothermal fluids. Geochemical data indicate that CFC formation was mainly caused by the hydrochemical precipitation of material from seawater. This process was accompanied by diagenetic phenomena, water-rock interaction, and influence of volcanic and hydrothermal sources.

Abundance of plankton in the upper 200 m layer in tropical oligotrophic regions of the Pacific and Indian Oceans

Quantitative distribution of plankton (mostly mesoplankton) is studied in the upper 200 m layer of oligotrophic waters in tropical anticyclonic gyres of the Pacific and Indian Oceans. Some general features of its trophic and taxonomic structures and vertical distribution are described.

Nutrition of species of the genus Amphiophiura in the Pacific and Indian Oceans

Nutrition of 6 deep-sea ophiuroid species of the genus Amphiophiura in the Pacific and Indian Oceans has been studied. One species is a detritus-feeder while the others are carnivorous. All 6 are widespread in deep-sea eutrophic regions of both oceans. Carnivorous species are also necrophagous, feeding on dead fish, surface pteropods, and crustaceans. Fishes are consumed mainly in the Indian Ocean, pteropods in the Pacific. Thus, as shown by carnivorous Amphtophiura, the rain of dead surface pelagic organisms is one of the most important sources of food for a number of deep-sea bottom-dwelling invertebrates.

(Table 7) Composition of rainwater collected over the Pacific and Indian Oceans in 1955-1960

Devoted to chemical interaction between the ocean and the atmosphere in the Pacific and Indian Oceans measured in 1955-1960.

(Table 1) Positions of the Mesocena elliptica zone in sediment cores from the Pacific and Indian Oceans

The Mesocena elliptica Ehr. zone in deep-sea sediments of the Pacific Ocean is characterized by a short vertical range at the base of the Pleistocene section. Depending on sedimentation rate this zone lies at various depths below the ocean bottom. M. elliptica is unknown in recent oceanic plankton. In fossil state known species indicate that sediments containing them are of Oligocene-Miocene age. New data obtained in early 1960's show that within a short interval, evidently in Early Pleistocene, M. elliptica was abundant in plankton, primarily in tropical regions. Correlation of paleomagnetic data with results of diatom analysis shows that the Mesocena elliptica zone always lies above the Pliocene-Pleistocene boundary, and that maximum contents of M. elliptica coincide with the Jaramillo event (0.85-0.95 million years ago).

(Table 1) Positions of the Mesocena elliptica zone in sediment cores from the Pacific and Indian Oceans

The Mesocena elliptica Ehr. zone in deep-sea sediments of the Pacific Ocean is characterized by a short vertical range at the base of the Pleistocene section. Depending on sedimentation rate this zone lies at various depths below the ocean bottom. M. elliptica is unknown in recent oceanic plankton. In fossil state known species indicate that sediments containing them are of Oligocene-Miocene age. New data obtained in early 1960's show that within a short interval, evidently in Early Pleistocene, M. elliptica was abundant in plankton, primarily in tropical regions. Correlation of paleomagnetic data with results of diatom analysis shows that the Mesocena elliptica zone always lies above the Pliocene-Pleistocene boundary, and that maximum contents of M. elliptica coincide with the Jaramillo event (0.85-0.95 million years ago).

Hydrocarbons in surface waters of the Atlantic and Indian Oceans

Results of investigation of various forms of oil pollution, i.e. oil films, tar, and hydrocarbons in the Northeast Atlantic Ocean and North Indian Ocean during October-December 1980 and February-May 1981 are presented. Oil pollution was found only in regions of the heaviest ship traffic and was somewhat less than in 1976-1977. Background concentration of non-polar hydrocarbons was 8-10 ?g/l in surface waters and 14 ?g/l in the shelf zone. Infrared spectroscopy and gas-liquid chromatography indicate that hydrocarbons occurring at concentrations exceeding 50 ?g/l have composition differing from background hydrocarbons. There is considerable accumulation of hydrocarbons in the thin surface layer, and they exist in different forms close to pollution sources.

(Table 8, page 38) Spectrographic analyses of deep sea manganese nodules from the Pacific and Indian Oceans

In an earlier paper by two of the authors the conclusion was reached that the 33 recognized species of oxides of Mn could be separated into 3 groups: 1) those which appeared to be persistently supergene in origin, 2) those which appeared to be persistently hypogene, and 3) those which were supergene in some localities and hypogene in other localities. When that paper was written, there were available about 250 X-ray diffraction analyses of mineral specimens, also 35 complete and about 150 partial chemical analyses. The conclusions of that paper were based upon the interpretation of the geologic conditions under which these specimens occurred. Late in the preparation of that paper, it seemed worthwhile to make numerous semiquantitative analyses of specimens, largely from 9 western [U.S.A] states, selected carefully from 5 groups of geologic environments, in the hope that the frequency and percentages of some elements might be distinctive of the several geologic groups. For this purpose, 95 specimens were selected from the 5 groups, as follows: 19 specimens interpreted as supergene oxides by the geologists who collected them, 35 specimens of hypogene vein oxides, 22 specimens of Mn-bearing hot spring aprons, 9 specimens of stratified oxides, and 10 specimens of deep-sea nodules. The spectrographic analyses here recorded indicate that a group of elements - W, Ba, Sr, Be, As, Sb, Tl, and Ge - are present more commonly, and largely in higher percentages, in the hypogene oxide than in the supergene oxides and thus serve to indicate different sources of the Mn. Also, the frequency and percentages of some of these elements indicate a genetic relation of the manganese oxides in hypogene veins, hot spring aprons, and stratified deposits. The analyses indicate a declining percentage of some elements from depth to the surface in these 3 related groups and increasing percentages of some other elements. It is concluded that some of the elements in deep-sea nodules indicate that sources other than rocks decomposed on the continents, probably vulcanism on the floors of the seas, have contributed to their formation.