首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 31 毫秒
1.
A simple weighing method using carbon tetrachloride as solvent was used to survey the dissolved hydrocarbon and tarball levels in the area of the Egyptian Red Sea coast. The area of investigation covers the coastal area from Ras-Gharib down to the port of Qosier during the period from September 1979 to February 1981. This survey confirms the presence of extensive oil pollution in the area, especially at Ras-Gharib and Ras-Shukhair. Minimum concentrations were obtained at Ghardaqa where no dissolved hydrocarbons were detected (i.e. less than 10 μg l?1) in 1979–1980 but an increase to 20 μg l?1 in 1981 was recorded. The high levels of pollution recorded in the southern part of the Gulf of Suez are related to the presence of the offshore oil fields, most of which are located at Ras-Gharib.  相似文献   

2.
Aliphatic (AHs) and polycyclic aromatic hydrocarbons (PAHs) were analyzed in dissolved and particulate material from surface microlayer (SML) and subsurface water (SSW) sampled at nearshore observation stations, sewage effluents and harbour sites from Marseilles coastal area (Northwestern Mediterranean) in 2009 and 2010. Dissolved and particulate AH concentrations ranged 0.05–0.41 and 0.04–4.3 μg l−1 in the SSW, peaking up to 38 and 1366 μg l−1 in the SML, respectively. Dissolved and particulate PAHs ranged 1.9–98 and 1.9–21 ng l−1 in the SSW, amounting up 217 and 1597 ng l−1 in the SML, respectively. In harbours, hydrocarbons were concentrated in the SML, with enrichment factors reaching 1138 for particulate AHs. Besides episodic dominance of biogenic and pyrogenic inputs, a moderate anthropisation from petrogenic sources dominated suggesting the impact of shipping traffic and surface runoffs on this urbanised area. Rainfalls increased hydrocarbon concentrations by a factor 1.9–11.5 in the dissolved phase.  相似文献   

3.
The concentration levels of Cd (25 ng l?1), Cu (0.45 μg l?1), Ni (0.48 μg l?1), Fe (0.2–7.0 μg l?1), Pb (40 ng l?1) and Zn (0.80 μg l?1) have been determined in the Danish Sounds and in the Kattegat. Different sampling techniques have been used and analyses have been carried out separately by two different investigators, both using freon-extraction followed by determination by atomic absorption spectrometry (a.a.s.). Except for iron, found mainly in the particulate phase, the metals are found predominantly in a dissolved and labile (extractable) form. The results are compared with trace metal levels found in the two main water masses entering the Kattegat—the North Sea and the Baltic Sea.  相似文献   

4.
The study aimed to determine the spatial distribution of n-alkanes and polycyclic aromatic hydrocarbons (PAHs) in surface sediments of the Segara Anakan nature reserve and their potential origins using gas chromatography–mass spectrometry. Total alkane concentrations ranged from 3755 to 129,027 μg kg−1, and the concentrations of 16 PAHs ranged from 375 to 29,517 μg kg−1. The ratios of specific n-alkanes (e.g., CPI24–34, WaxCn, and Paq), including a new proposed index, terrestrial–marine discriminant (TMD), as well as the ratios of selected PAHs (e.g., Ant/∑178, Fl/∑202, BaAnt/∑228, and IPyr/∑276), showed that the sources of hydrocarbons in the sediments were generally biogenic, including both terrigenous and marine, with an anthropogenic pyrolytic contribution (petrogenic and biogenic combustion). For the environmental risk assessment, a sediment quality guideline (SQGs) comparison indicated that the station risk levels ranged from low to medium-low, except for R6, which has a greater impact on the ecological risk for marine organisms.  相似文献   

5.
Bulk hydrocarbon deposition rates have been measured over a 15 month period at four stations in south-eastern Virginia surrounding the lower Chesapeake Bay. A nearly linear trend of atmospheric particulate deposition was recorded. Deposition rates at the urban station (195 μg m?2 day?1) were aproximately three times greater than those recorded for nonurban and coastal locations (mean value 69 μg m?2 day?1). The increased levels at the urban location were attributed to localized source inputs. Anthropogenic hydrocarbons accounted for approximately 50% of the total deposition at all stations. Significant biogenic inputs were indicated by the odd/even n-alkane distribution. A minimum flux to the water surface, based on mean nonurban deposition rates (24 mg yr?1), indicated an annual particulate hydrocarbon flux of +275 metric tons. Little information is available for the comparison of additional source inputs; however, the data reported here indicate that the aerial deposition of hydrocarbons is of the same order of magnitude as the input from municipal wastewater facilities and accidental discharge and is a potentially significant source of hydrocarbon pollution to the Chesapeake Bay Estuary.  相似文献   

6.
Petroleum hydrocarbons in the sediments of the Bothnian Bay, Baltic proper, Öresund, Kattegatt and Skagerrak were analysed in a survey of oil pollution along the Swedish coast in 1974 and 1975. Sixty-one of these sediment stations were revisited in 1982 and analysed with the methods used in the first survey. The mean content of petroleum hydrocarbons (paraffin-naphthene fraction) in the sediment surface showed a statistically significant increase from 199 to 252 μg g?1 dry wt. The main increase had taken place in the coastal areas. Within 0–20 km distance of urbanized areas (>20 000 inhabitants) petroleum hydrocarbons had increased from 371 to 447 μg g?1. Sediment levels increased from 76 to 117 μg g?1, 20–50 km from urbanized areas. The increase in these areas was equivalent to 0.119 g m?2 yr?1.  相似文献   

7.
The composition characteristics of light hydrocarbons from crude oil, chloroform bitumen A, saturated hydrocarbon fraction, aromatic hydrocarbon fraction, and asphaltene fraction during cracking have been studied systematically. The results revealed that the content of n-alkanes, branched alkanes and cycloalkanes in light hydrocarbons from the samples gradually decreased as the simulation temperature increased, and finally almost depleted completely, while the abundance of methane, benzene and its homologues increased obviously and became the main products. The ratios of benzene/ n-hexane and toluene/n-heptane can be used as measures for oil cracking levels. Variation characteristics of maturity parameters of light hydrocarbons, for example, iC4/nC4, iC5/nC5, isoheptane value, 2,2-DMC4/nC6, and 2-MC6+3-MC6/nC7 for different samples with increasing pyrolysis temperature, are consistent with those in petroleum reservoirs, indicating that these parameters may be efficient maturity index.  相似文献   

8.
The higher boiling point range of saturated aliphatic hydrocarbon fractions extracted from North Sea water have been re-investigated in detail with improved high resolution glass capillary columns suitable for high temperature gas-chromatography. The resulting chromatograms reveal hydrocarbon patterns, most of which have the same common feature: a smooth distribution of the long-chain n-alkanes combined with a lack of the branched alkanes normally expected for fossil fuel oil. Instead, two homologous series of iso- and anteiso-alkanes could be detected. Since this finding is always associated with traces of present or past fossil fuel oil contamination of the upper water column, these environmental n-, iso and anteisoalkanes are considered to be recently ‘bio-converted’ from fossil fuel oil hydrocarbons. They form a third group beside recent biogenic and fossil petrogenic hydrocarbons in the marine environment. Oil pollution records of the marine environment will have to take into account this group of microbial hydrocarbons.  相似文献   

9.
The molecular distribution and compound specific stable carbon and hydrogen isotope ratios were measured on solvent extractable hydrocarbons from the Late Paleoproterozoic McArthur River, or “Here's Your Chance” (HYC) Pb/Zn/Ag ore deposit in the Northern Territory of Australia. Five samples were collected from the McArthur River mine on a northeast–southwest transect in order to sample a gradient of hydrothermal alteration. One sample was taken from the unmineralized W-Fold Shale unit immediately below the HYC ore deposit. δD of n-alkanes, branched alkanes and bulk aromatic fractions were measured, and δ13C of n-alkanes, polynuclear aromatic hydrocarbons (PAHs) and bulk kerogen were measured to assess the isotopic effects of a varying degree of hydrothermal alteration on different components of HYC organic matter (OM). Relative to n-alkanes in Barney Creek Formation sediments that did not undergo mineralization, HYC n-alkanes are enriched in deuterium (D) by 50–60‰. This is likely to be a result of equilibrium hydrogen exchange during ore genesis with a highly D-enriched fluid that originated in an evaporitic basin. Trends with distance along the sample transect are ambiguous, but from the northernmost to southernmost point, n-alkanes are less D-enriched, and PAHs are less abundant and less 13C-enriched. This could be due to decreasing hydrothermal alteration effects, decreasing delivery of highly altered OM by the mineralizing fluid, or both. The carbon isotopic composition of HYC PAHs is inconsistent with a Barney Creek Fm source, but consistent with an origin in the underlying Wollogorang Formation. PAHs are 13C-depleted relative to n-alkanes, reflecting a kerogen source that was 13C-depleted compared to n-alkanes, typical for Precambrian sediments. PAHs are more 13C-depleted with increasing molecular weight and aromaticity, strengthening the case for a negative isotopic effect associated with aromatization in ancient sediments. Together, these data are consistent with a an ore deposition model in which fluids originated in an evaporitic deposit lower in the basin and interacted with metals and OM in the Tawallah Group at temperatures above 250 °C and a depth of ~ 6 km before ascending along a flower structure associated with the Emu Fault and cooling to 200 ± 20 °C before reaching Barney Creek sediments.  相似文献   

10.
Petroleum mainly comprises carbon and hydrogen elements. The stable carbon isotopic analysis for whole oil was undertaken as early as the 1930s. After decades, the stable carbon isotopic analytical methods have been developed from analysis for whole oil and oil fractions (e.g., saturated, aromatic and polar frac-tions) into compound-specific isotopic analysis with the emergence of the newly developed GC-C-IRMS analytical technique. Especially, by using com-pound-specific isotopic analytical…  相似文献   

11.
Near-bottom currents, light transmission and scattering, and bottom pressure were measured with GEOPROBE tripods and vector-averaging current meters during June 1979 to April 1980 on the central shelf 10 km west of the Russian River, California. The instruments were located on the mid-shelf mud belt composed of bimodal sandy clayey silts contributed principally by the Russian River. During the summer season of persistent northwesterly, upwelling-favorable winds, the average and maximum current speeds 5 m above the bottom were 11 and 31 cm s?1, respectively. The mean (subtidal) flow at 5 m above bottom was poleward and slightly offshore at about 6 cm s?1. The strongest wave-generated bottom currents were about 10 cm s?1, but oscillatory velocities > 5 cm s?1 were infrequent. Suspended-matter concentrations, derived from the optical data at 1.9 m above the bottom, ranged from 1 to 6 mg l?1. The optical data show that the currents and waves were generally below threshold levels for sediment erosion through the summer. In contrast, during the autumn and, particularly, the winter months, the average and maximum concentrations of suspended matter increased substantially. The increases were primarily caused by larger waves from distant storms and short intervals of strong currents associated with local storms and, secondarily, by the large seasonal flow of the Russian River. Wind-driven and wave-generated bottom currents were as large as 37 and 45 cm s?1, respectively, during local storms in December 1979 and February 1980. Suspended-matter concentrations averaged about 7 mg l?1 during non-storm winter periods, but increased to nearly 150 mg l?1 during a December storm. Estimates of suspended-matter flux near the bottom show that the local winter storms, which had a combined duration of about 12 days, could account for 30 to 50% of the total annual suspended-sediment transport at the mid-shelf site. Although intervals of large swell were at times superimposed on southward advective currents, the major sediment-transport events were caused by strong southerly winds that produced poleward bottom currents with a significant offshore component. The primary aspects of the distribution of modern sediments on this shelf are in good agreement with the observed poleward transport.  相似文献   

12.
The levels of selected organic markers, including 17 polycyclic aromatic hydrocarbons (PAHs), 16 of which are classified as priority pollutants by the US-EPA and perylene, aliphatic hydrocarbons (total and linear alkanes) and petroleum biomarkers (hopanes and steranes), were measured in suspended particulate matter (SPM) of the Mundaú-Manguaba estuarine-lagoon system (MMELS) in northeastern Brazil and the Paraíba do Sul River (PSR) estuary in southeastern Brazil, both of which are affected by sugarcane agriculture and urbanization. A total of 33 surface water samples of SPM were collected (22 from the MMELS and 11 from the PSR). The ∑16PAH ranged from 221 to 1243 ng g−1 in the MMELS and from 228 to 1814 ng g−1 in the PSR. Hopane and sterane concentrations in the PSR were higher than in the MMELS due to the input from petrogenic sources in PSR. The contributions of higher plants were also observed by n-alkane analyses. The PAH isomeric ratios indicated that the SPM from MMELS showed characteristics of combustion from biomass or petroleum and PSR was associated to petrogenic input, either from combustion or from unburned petroleum. Three sampling sites located near to the sugarcane plant and mouth of the rivers showed higher PAH concentrations and may largely be considered as highly contaminated. However, levels of n-alkanes and petroleum biomarkers in both study areas were relatively low.  相似文献   

13.
The rigin and fate of six phthalate esters (dimethyl phthalate (DMP), diethyl phthalate (DEP), di‐n‐butyl phthalate (DnBP), butyl benzyl phthalate (BBP), di (2‐ethylhexyl) phthalate (DEHP) and di‐n‐octyl phthalate (DnOP)), were investigated during 2005 and 2006 in the densely populated Seine river estuary. Four compounds, DMP, DEP, DnBP and DEHP were detected at all the stations with DEHP (160–314 ng L?1), followed by DEP (71–181 ng L?1) and next DnBP (67–319 ng L?1), except at la Bouille, where DnBP was the second most important compound. BBP and DnOP concentrations remained low and were not found at all the stations. Considering all six phthalates, Caudebec‐en‐Caux (beginning of the salinity gradient) was the least polluted station (464 ng L?1), whereas Honfleur (771 ng L?1) and La Bouille (716 ng L?1) displayed the highest contamination levels, probably related to important industrial plants. From Caudebec‐en‐Caux to Honfleur (maximum turbidity), variation of DEHP concentration was related to that of suspended matter. In addition, the salinity rise in that area might have facilitated DEHP sorption upon particles. A significant correlation between flow magnitude and DEHP concentration was found (P < 0·01, n = 12), supporting the influence of the hydrological cycle upon contamination. Runoff contribution (56·9 kg d?1) to river contamination was confirmed by the annual evolution of phthalate concentrations in the Seine river at Poses. Concentrations of DEHP in the tributaries were in the same range as those of the Seine River (100–350 ng L?1), except for two in densely populated and industrialized areas: Robec (800 ng L?1) and Cailly (970 ng L?1). The treatment plant discharge fluxes were in the same range as those of tributaries (30·4–250 g d?1). During high flow periods, the influence of tributaries and of treatment plants seemed to play a minor part in the contamination level of the Seine river estuary. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   

14.
Based on kerogen-generated hydrocarbon model, a new method to calculate hydrocarbon yields for coals and coaly samples was put forward by means of pyrolysis technique. At the same time, the empirical criteria suggested by Powell were revised. The threshold value was preliminarily defined as HC yields >30 mg HC per gram TOC for effective gas source rocks and >60 mg HC per gram TOC for effective oil source rocks. Additionally, it was also confirmed that the relative compositions of the three ranges of C1-C5 total hydrocarbons, C6-C14n-alkanes plusn-alkenes and C15+ n-alkanes plusn-alkenes from pyrolysates can be effectively used to distinguish the coal-generated hydrocarbon types.  相似文献   

15.
Danube river water samples were saturated with mineral oil, and then the primary production (gross) was determined by means of the light-dark bottle method (oxygen) in situ at depths of 0.1… 1.5 m in comparison with untreated samples. Samples were exposed for half a solar day alternately during the first and second half-days. Investigations carried out between March and October for periods of 14 days showed a mean production of 2.56 g · m?2d?1 O2, which was reduced by 36% due to 12.6 mg/l hydrocarbons. Production decreases with the water depth from 6.2 to 0.9 mg · l?1d?1 02, whereas the inhibition by hydrocarbons increases from 31 to 41%.  相似文献   

16.
The concentration of dissolved mercury in sea water has been determined in a number of areas in the northern and southern hemispheres and an attempt has been made to correlate the values found for certain areas with natural physical phenomena. The average concentrations found ranged from 11.2 ng l?1 in the southern hemisphere to 33.5 ng l?1 for the northern hemisphere; an increase suspected to be the result of dispersion of industrial pollution by jet streams. Local effects including upwelling, volcanic action, land run-off and heavy suspended matter loads are also discussed.  相似文献   

17.
Between January 1978 and September 1979 samples of subsurface (1 m) water and surface sediment were collected from sites in the North Sea, English Channel, Irish Sea and a number of estuarine areas. These have been analysed by fluorescence spectroscopy (UVF) in order to provide information on the levels of hydrocarbons generally present in UK marine waters.Total hydrocarbon concentrations (THCs) of water samples ranged from 1.1–74 μg l.?1 Ekofisk crude oil equivalents, all values greater than 3.5 μg l.?1 occurring inshore. In offshore areas the mean THCs were: 1.3 μg l.?1 in the northern North Sea, 1.5 μg l.?1 in the western Channel, 2.5 μg l.?1 in the eastern Channel and southern North Sea, and 2.6 μg l.?1 in the Irish Sea.THCs of sediment samples ranged from 0.27–340 μ g?1 dry weight Ekofisk crude oil equivalents, the highest concentration being in the Queen's Channel, the main entrance to the River Mersey.  相似文献   

18.
Laboratory reared veliger larvae of the common mussel Mytilus edulis were grown for 15 days in filtered seawater containing 10 μg l?1, 1 μg l?1 and 0.1 μg l?1 tributyltin oxide (TBTO), the biocide in recent antifouling paint formulations. No larvae survived longer than 5 days in 10 μg l?1 TBTO or 10 days in 1 μg l?1 TBTO. Approximately half the larvae subjected to 0.1 μg l?1 TBTO were dead by day 15 (approximate 15 day LC50 = 0.1 μg l?1 TBTO) and most of the surviving larvae were moribund and had grown significantly more slowly than controls. It is noted that current recorded levels of TBT at several UK estuarine sites are higher than 0.1 μg l?1 and there has therefore probably been a high mortality of mussel larvae at such sites. The results are discussed in relation to the reported short-term toxicity of organotins to other marine organisms and the value of carrying out longer-term tests at low levels of TBT is pointed out.  相似文献   

19.
The concentration of petroleum hydrocarbons in Arctic surface water under the ice north of Svalbard has been determined by fluorescence spectrofluorometry using three different excitation/emission wavelength combinations. With Kuwait crude oil as a reference, the concentration range is 0.1–0.6 μg l?1 crude oil equivalents with respect to light molecular weight components and 0.05–0.2 μg l?1 heavy molecular weight components.  相似文献   

20.
Seven short sediment cores from the southern Okinawa Trough were collected and analyzed for the aliphatic hydrocarbon concentrations by capillary gas chromatography to explore the deposition of hydrocarbons to this area. For all cores studied, ratios of Σhydrocarbons/TOC, (nC27+nC29+nC31)/TOC, terrigenous/aquatic, and diploptene/ΣC25–33n-alkanes fluctuated around a mean value with coefficients of variation ranging from 9.0% to 19.7%, 4.9% to 20.0%, 27.3% to 129%, and 3.8% to 163%, respectively. For the nC31/(nC27+nC29+nC31) ratio, only station 21 showed fluctuation. Moreover, the carbon preference indexes in the C25–C33n-alkane range also exhibited fluctuating values with coefficients of variation of 1.9–14.4%. These results indicate that concentrations of hydrocarbon inputs to the sampling sites vary with time; this may result from complex current flow and sediment transport, leading to variable lipid deposition. In addition, significant correlation between diploptene (hop-22(29)-ene) and higher plant n-alkanes was found for cores 21, 42 and 46, indicating that diploptene was predominantly from higher plant sources. However, no correlation between diploptene and higher plant n-alkanes was found for cores 20, 36, 43 and 44; autochthonous sources of diploptene in these cores were quite probable.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号