31 resultados para MPC

em Publishing Network for Geoscientific


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It is found that hydrocarbons are constantly accumulated on the main geochemical barriers: water-atmosphere, river-sea, water-suspended matter, and water-bottom sediment interfaces. Degree of hydrocarbon accumulation reaches 13.5-17.6 in the surface microlayer and exceeds 1000 in bottom sediments. Hydrocarbon composition changes in this process. Local pollutant loads result in accumulation of polycyclic aromatic hydrocarbons by bottom sediments and benzo(a)pyrene concentration sometimes exceeds MPC. Content of hydrocarbon migratory forms is calculated.

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With the exception of a brief (2 m.y.) late Miocene-early Pliocene hiatus, an essentially complete Neogene record was recovered on the Kerguelen Plateau in a calcareous biofacies. The stratigraphic distribution of about 30 taxa of Neogene planktonic foraminifers recovered at Sites 747, 748,and 751 (Central and Southern Kerguelen plateaus; approximately 54°-58°S) is recorded. Faunas are characterized by low diversity and high dominance and exhibit a gradual decline in species numbers (reflecting a concomitant increase in biosiliceous forms, particularly diatoms) from about 10 in the early Miocene to 5-8 in the middle Miocene, 3-4 in the late Miocene, to essentially a lone (Neogloboquadrina pachyderma) form in the Pliocene-Pleistocene. A provisional sevenfold biostratigraphic zonation has been formulated that, together with the recovery of a representative Neogene magnetostratigraphic record, may ultimately lead to a correlation with low-latitude magnetobiostratigraphies. The initial appearance of Neogloboquadrina pachyderma is associated with magnetic polarity Chron (MPC) 4 (~7 Ma) and MPC 4A (>8 Ma) at Sites 747 and 751, respectively.

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By means of spectrographic analysis 96 samples of marine sediments were analyzed quantitatively for V, Ti, Zr, Co, Ni, Sc, Cr, and La, and semi-quantitatively for Ba and Sr. Ca has been estimated by visual comparison of spectrographic plates, and several Fe values have also been determined in the same way. Geographically 40 of these samples are from the Pacific Ocean basin, one of which is a manganese nodule, 21 from the Gulf of Mexico, 11 from Atchafalaya Bay, 8 from American Devonian to Miocene sedimentary rocks, 4 from the Mississippi Delta, 3 from the San Diego trough, 3 from off Grand Isle, 3 from Lake Pontchartrain, from Bay Rambour, 1 from Laguna Madre off the Texas coast, and 1 from the Guadalupe River, Texas. The afore-mentioned elements were sought using PdCl2 as an internal standard, after the method developed by Ahrens (1950) and his co-workers. Samples were run in duplicate, and standard deviations varied from 5 to 14 percent. Working curves, from which final values were obtained, were constructed with the use of standard granite, G1, and the standard diabase, W1, as standards. See Fairbairn and others (1951). An experiment was carried out to determine the effect of matrix change, involving CaCO3, on the spectral line intensities of the quantitatively analyzed elements. The distribution of each of the elements is discussed separately, and particular emphasis is given to oceanic "red clay", in which many elements are enriched. A general discussion is given to mineralogy of the sediments, cation exchange in its bearing on this thesis, and a brief recount of the two hypotheses of origin of oceanic "red clay". An application of the findings of this thesis to aid in the choice of the more likely hypothesis is made.

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Average quantitative spectrographic data are presented for V, Ti, Zr, Ni, Co, Sc, Cr and La in the following Pacific deep-sea cores: siliceous ooze (3), red clay (6), volcanic mud (3), calcareous ooze (3) and one manganese nodule, and in 23 near-shore cores, mostly from the Gulf of Mexico.

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The cores described in this report were taken on MIDPAC (Middle Pacific) Expedition in August-September 1950 by Scripps Institution of Oceanography from, the R/V Horizon. A total of 106 cores and dredges were recovered and are available at Scripps for sampling and study. The coring sites, all in the tropical central Pacific.