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991.
992.
Observation of clouds and solar radiation over the Pacific Ocean as relation to global climate
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Farn Parungo Clarence Nagamoto Cecilia M. I. R. Girz Jeff Torgerson Zhou Mingyu 《海洋学报(英文版)》1995,14(2):201-207
ObservationofcloudsandsolarradiationoverthePacificOceanasrelationtoglobalclimate¥FarnParungo;ClarenceNagamoto;CeciliaM.I.R.Gi... 相似文献
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Seismic stratigraphic and main lithological features of the sedimentary cover overlying the basement of the Alboran Sea were established via the analysis of commercial multichannel seismic surveys, geophysical well logs, and well data. Six seismic stratigraphics units (VI to I), bounded by unconformities, form the marine sediments that range in age from early Miocene to Quaternary. They are dated by extrapolation of commercial drilling results from the northern Alboran Sea. Volcanic activity is recorded within sedimentary sequences of units V to II. Undercompaction features are detected in the two basal units. 相似文献
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The flux and compositions of solvent-extractable lipid fractions were measured in particulate matter collected periodically by moored sediment traps in the Santa Monica Basin from 1985–1988. The purpose was to assess the compositional changes during settling, the carbon dynamics in the basin and to estimate the impacts of energy-related by-products on the surface sediments. Sediment traps recorded consistently high lipid fluxes in the eastern slope relative to the central basin, reflecting elevated terrigenous carbon inputs possibly from land-based human activities. Generally, lipid fluxes decrease offshore but increase vertically with water depth below 500m, implying lateral transport of particles. The steep decline of flux in the top 500m of the water is related to the rapid decomposition and mineralization of the marine-derived cellular carbon compounds. Less than 5% of the marine lipid components reach the seabed. In contrast, preferential preservation of terrigenous lipid is clearly evident from the chemistry of deeper traps and surface sediments.The lateral transport of particles is reflected in the presence of higher plant-derived lignin phenols and sewage-derived coprostanol and epicoprostanol in the deep trap material as well as in surface sediment throughout the basin. Petroleum triterpanes characteristic of natural seepage also permeates through the entire basin. Based on the data collected from both the trap particulte matter and surface sediments, a carbon budget for the Santa Monica Basin has been constructed. 相似文献
998.
Freshly prepared homogenates were used to assess the relative ability of winter flounder (Pseudopleuronectes americanus) liver and intestinal mucosal cells to metabolize the polycyclic aromatic hydrocarbon (PAH) benzo[a]pyrene (BaP) and its proximate carcinogenic metabolite, BaP-7,8-dihydrodiol (7,8-Diol). Data obtained from homogenates prepared from fish previously fed β-naphthoflavone (BNF) indicated that both tissues had similar abilities to metabolize either BaP or 7,8-Diol on a per gram of protein basis. Metabolite profiles produced indicate that water-soluble metabolite formation is favored at low doses. These findings support the hypothesis that the intestine plays an important role in first-pass metabolism of dietary carcinogens in the winter flounder. 相似文献
999.
The concentration of carbon disulfide (CS2) in surface water and relevant hydrographic parameters were determined in coastal waters of the eastern USA (Delaware Bay and Chesapeake Bay, including the Potomac River; 7–11 September 1986). The CS2 concentration varied extensively along the cruise track, from 4 to 510 pmol S(CS2) l−1 (n = 103). The average values in estuarine, shelf, and oceanic waters were found to be 118 ± 100 pmol S(CS2) l−1 (n = 54), 51 ± 34 pmol S(CS2) l−1 (n = 14), and 28 ± 12 pmol S(CS2) l−1 (n = 35), respectively. To help interpret the geochemical behavior of CS2, we analyzed the depth distribution of CS2 in the North Atlantic Ocean during an earlier cruise (23 April–2 May 1986). In most cases, these depth profiles show a near-surface maximum at about 10–20 m depth and a relatively steep gradient below this maximum. Based on the distribution pattern in the water column and evidence provided by earlier workers, we propose that diffusion of CS2 from bottom sediments may contribute to CS2 levels in surface seawater. The atmospheric concentration of CS2 was also investigated at some locations during the September cruise. Except during periods when there was a significant anthropogenic input, the concentration of CS2 in air was generally in the range of 4–15 pptv (parts per trillion by volume) with a mean of 10.4 ± 4.0 pptv (n = 10). The calculated sea-to-air emission rates of CS2 at each of our sampling stations show a decreasing trend across estuarine, shelf, and oceanic areas, in agreement with the trend in surface water concentrations. 相似文献
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