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The isolation and quantification of the various sources of trace levels of hydrocarbons in environmental samples is a difficult analytical task. Based on the hydrocarbon concentrations found in non-polluted surface sediment and an estimate of the amounts of coal particles found in similar areas we conclude that unburned coal can be a significant source of sediment hydrocarbons in the coastal marine environment. 相似文献
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Curie depth determination from aeromagnetic spectra 总被引:6,自引:0,他引:6
R. T. Shuey D. K. Schellinger A. C. Tripp L. B. Al 《Geophysical Journal International》1977,50(1):75-101
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Peacock EE Hampson GR Nelson RK Xu L Frysinger GS Gaines RB Farrington JW Tripp BW Reddy CM 《Marine pollution bulletin》2007,54(2):214-225
Petroleum hydrocarbons persist in salt marsh sediments in Winsor Cove (Buzzards Bay, Massachusetts) impacted from the 1974 spill of No. 2 fuel oil by the barge Bouchard 65. Intertidal sediment cores were collected from 2001 to 2005 and analyzed for total petroleum hydrocarbons (TPHs). TPHs content was greatest (as high as 8.7 mg g(-1) dry weight) in the surface sediments and decreased with distance landward. Select samples were analyzed for polycyclic aromatic hydrocarbons (PAHs) with values as high as 16.7 microg g(-1) for total naphthalenes and phenanthrenes/anthracenes. These remaining PAHs are mainly C(4)-naphthalenes and C(1)-, C(2)-, and C(3)-phenanthrenes/anthracenes revealing preferential loss of almost all of the naphthalenes and the parent compound phenanthrene. Inspection of the data indicates that biodegradation, water-washing and evaporation were major removal processes for many of the petroleum hydrocarbons in the marsh sediments. In addition, historical data and photographs combined with their recent counterparts indicate that erosion has physically removed these contaminants from this site. 相似文献
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William "Tripp" Fischer 《Ground Water Monitoring & Remediation》2003,23(2):56-63
For regulators to develop risk-based screening levels (RBSLs) for a petroleum constituent, a maximum allowable concentration at an exposure point, such as a drinking water action level, must be established. Of particular interest to regulators of leaking underground storage tank (LUST) sites in Delaware is the development of RBSLs for the oxygenated compounds that are added to gasoline to increase octane rating and promote cleaner burning fuel. Whereas methyl-tertiary butyl ether (MTBE) became the first of the oxygenated compounds to gain regulatory attention in Delaware, tertiary-butyl alcohol (TBA) is not far behind. TBA has been detected at LUST sites throughout Delaware and in some cases has been detected in private water supplies. However, Delaware does not currently have a drinking water action level, or maximum allowable exposure concentration, on which to base regulatory decisions regarding TBA.
Toxicological data is inconclusive in classifying TBA as a carcinogen. However, carcinogenic responses are reported in rat and mice studies at extremely high doses. To address TBA in Delaware's Risk-Based Corrective Action Program, the Delaware Division of Public Health must calculate drinking water action levels based on the results of the toxicological data. However, the establishment of TBA action levels could have a tremendous impact on the costs associated with investigating and remediating a LUST site. TBA may add $2000 to $5000 per year in analytical costs alone for an average LUST site in Delaware. 相似文献
Toxicological data is inconclusive in classifying TBA as a carcinogen. However, carcinogenic responses are reported in rat and mice studies at extremely high doses. To address TBA in Delaware's Risk-Based Corrective Action Program, the Delaware Division of Public Health must calculate drinking water action levels based on the results of the toxicological data. However, the establishment of TBA action levels could have a tremendous impact on the costs associated with investigating and remediating a LUST site. TBA may add $2000 to $5000 per year in analytical costs alone for an average LUST site in Delaware. 相似文献
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Far-UV echelle spectroscopy of the radio-quiet QSO H1821+643 (zem=0.297), obtained with the Space Telescope Imaging Spectrograph (STIS) at approximately 7 km s-1 resolution, reveals four definite O vi absorption-line systems and one probable O vi absorber at 0.15相似文献
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Following previous work on bounds for complex dielectrics, bounds on the complex conductivity of a mixture of two isotropic components can be developed which are independent of any special assumption concerning the geometry of the mixture. If certain broad restrictions are assumed, such as isotropy of the mixture, then the bounds can be made more restrictive. These bounds reveal the range of the induced polarization response which can be caused by a mixture of two materials of known complex conductivity. The bounds can also be generalized for spectral responses. The bounds are conservative lithologically in the sense that many of the special models corresponding to boundary responses have lithological counterparts. The chief use for the given bounds is to gain insight into the nature of the induced polarization response. It is also possible to use the bounds to estimate the volume fractions of the components. We illustrate how this is done for the case of a general anisotropic medium. 相似文献