Accumulation of copper in the Permian Kupferschiefer: A result of post-depositional redox reactions     

W. Püttmann  H. Heppenheimer  R. Diedel   《Organic Geochemistry》1990,16(4-6)

Within the Central European Zechstein Basin the Permian Kupferschiefer has been deposited under anoxic conditions. In most parts of the basin, the metal content does not exceed values commonly observed in black shales. However, in areas near to the Zechstein sea-shore which are simultaneously related to rift zones a significant base metal enrichment is observed. Organic geochemical analyses of the copper-mineralized sections in the Kupferschiefer from Southwest Poland show that significant changes in the composition of organic matter are associated with the metal enrichment processes. Porphyrins, commonly abundant constituents of the shale, have been decomposed by oxidizing fluids. Additionally, aliphatic hydrocarbons have been largely removed from the bitumen and alkylated aromatic systems were affected by side-chain degradation. This particular type of alteration is explained by ascending oxidizing solutions which transported high amounts of base metals from Lower Permian red beds into the Kupferschiefer horizon acting as a geochemical trap. The metal precipitation is suggested to be a result of thermochemical sulphide production with organic matter acting as hydrogen source. In areas such as the Lower Rhine Basin in the bottom section of the Kupferschiefer the base metals lead and zinc as well as barium have been accumulated from basinal Carboniferous formation waters. Copper enrichment is not observed because potential source rocks are missing in this area. However, the observed compositional changes of the organic matter do not point towards thermochemical redox processes.  相似文献   

Ambient biogenic hydrocarbons and isoprene emissions from a mixed deciduous forest     

J. D. Fuentes  D. Wang  H. H. Neumann  T. J. Gillespie  G. Den Hartog  T. F. Dann 《Journal of Atmospheric Chemistry》1996,25(1):67-95

Experiments were conducted during the growing season of 1993 at a mixed deciduous forest in southern Ontario, Canada to investigate the atmospheric abundance of hydrocarbons from phytogenic origins, and to measure emission rates from foliage of deciduous trees. The most abundant phytogenic chemical species found in the ambient air were isoprene and the monoterpenes -pinene and -pinene. Prior to leaf-bud break during spring, ambient hydrocarbon mixing ratios above the forest remained barely above instrument detection limit (20 parts per trillion), but they became abundant during the latter part of the growing season. Peak isoprene mixing ratios reached nearly 10 parts per billion (ppbv) during mid-growing season while maximum monoterpene mixing ratios were close to 2 ppbv. Both isoprene and monoterpene mixing ratios exhibited marked diurnal variations. Typical isoprene mixing ratios were highest during mid-afternoon and were lowest during nighttime. Peak isoprene mixing ratios coincided with maximum canopy temperature. The diurnal pattern of ambient isoprene mixing ratio was closely linked to the local emissions from foliage. Isoprene emission rates from foliage were measured by enclosing branches of trees inside environment-controlled cuvette systems and measuring the gas mixing ratio difference between cuvette inlet and outlet airstream. Isoprene emissions depended on tree species, foliage ontogeny, and environmental factors such as foliage temperature and intercepted photosynthetically active radiation (PAR). For instance, young (<1 month old) aspen leaves released approximately 80 times less isoprene than mature (>3 months old) leaves. During the latter part of the growing season the amount of carbon released back to the atmosphere as isoprene by big-tooth and trembling aspen leaves accounted for approximately 2% of the photosynthetically fixed carbon. Significant isoprene mixing ratio gradients existed between the forest crown and at twice canopy height above the ground. The gradient diffusion approach coupled with similarity theory was used to estimate canopy isoprene flux densities. These canopy fluxes compared favorably with values obtained from a multilayered canopy model that utilized locally measured plant microclimate, biomass distribution and leaf isoprene emission rate data. Modeled isoprene fluxes were approximately 30% higher compared to measured fluxes. Further comparisons between measured and modeled canopy biogenic hydrocarbon flux densities are required to assess uncertainties in modeling systems that provide inventories of biogenic hydrocarbons.  相似文献   

Organic geochemistry of Cuban oils—I. The northern geological province     

P.G. Campos  J.O. Grimalt  L. Berdie  J.O. Lopez-Quintero  L.E. Navarrete-Reyes 《Organic Geochemistry》1996,25(8):475-488

The isoprenoid, hopanoid and steroid compositions of 15 oils from the most productive oil fields in Cuba were studied to determine source-rock depositional environments and organic matter sources. The oils, which are from the northern geological province of Cuba and can be defined by the position with respect to the overthrust belt, can be grouped into two families: those from the Remedios (1) and those from the Placetas (2) tectonostratigraphic units.Remedios oils contain 17α(H)-diahopane, high relative amounts of 18α(H)-22,29,30-trisnorneohopane and diasteranes, which is indicative of generation from clay-rich source rocks. The crude oils of the Placetas Unit exhibit a sterane/hopane composition consistent with a carbonate origin. Nevertheless, these polycyclic hydrocarbons exhibit significant changes in composition, indicating that several organic matter sources, e.g. a carbonate/evaporitic origin of Varadero and Varadero Sur oils, have contributed to the oils from this Unit. The Remedios oils are more mature [evaluated from the and sterane indices] than the Placetas oils.A wide range of biodegradation levels are encountered in these oils (from 0 to 7–8 using the scale derived by Volkman et al. (1983). The high relative abundance of 25-norhopanes is a distinctive feature of Remedios oils. The presence of these compounds in lightly biodegraded or nondegraded oils corresponds to a mixing of paleobiodegraded oil with more recently sourced nondegraded oil in the reservoir. The most biodegraded oil, Cantel, exhibits and sterane ratios, and hopane ratios that have been altered by microbial attack.  相似文献   

Hydrocarbons in Washington coastal sediments     

Fredrick G. Prahl  Roy Carpenter 《Estuarine, Coastal and Shelf Science》1984,18(6):703-720

The sources and distributions of polycyclic aromatic hydrocarbons (PAH) and aliphatic hydrocarbons are characterized in seventeen sediments from a highly river-influenced sedimentary environment off the southwestern coast of Washington. The major hydrocarbons are land-derived, introduced as preformed compounds and display long-term stability in sediment cores. A series of PAH of anthropogenic origin and two naturally derived compounds, retene and perylene, dominate the PAH composition in these sediments. Plantwax n-alkanes are the major aliphatic hydrocarbon constituents. Aliphatic hydrocarbons of marine origin, pristane and a series of four acyclic, multibranched C₂₅ polyolefins, are also observed in many sediments. The concentrations of these marine-derived hydrocarbons decrease to negligible levels rapidly with sediment depth from the sea-sediment interface, suggesting degradation.In general, the major land-derived hydrocarbons are concentrated in the midshelf silt deposit which extends northwestward along the continental shelf from the Columbia River mouth. A quantitatively more minor, natural series of phenanthrene homologs, also of terrestrial origin, is preferentially advected further offshore and deposited in continental slope sediments. These distributions are consistent with recognized particle associations for these compounds and sediment dispersal processes in this coastal environment. Sediment core records suggest the present pattern of dispersal has persisted for at least the past century and possibly since the Late Pleistocene.  相似文献   

厦门西海域表层水中PAHs污染与PAHs降解菌分布的关系   总被引：12，自引：0，他引：12  

田蕴  郑天凌  王新红  肖清江  张勇 《热带海洋学报》2003,22(6):15-21

在厦门西海域设置6个站位，于2001年7月和10月两个航次对各站位表层水中多环芳烃(polycyclic aromatic hydrocarbons，PAHs)的含量及几种常见PAHs的降解菌的数量进行调查，结果表明：表层水中PAHs的含量很不稳定，存在明显的时间变化。在7月的调查中，表层水中能检测到的PAHs以2—3环的为主，而在10月以46环的为主。低分子量的PAHs——芴和菲的含量与其降解菌的数量之间具有明显的正相关，而高分子量的PAHs—荧蒽和芘的含量与其降解菌的数量之间没有表现出相关性。  相似文献   

Sources and Transport of Particulate Hydrocarbons in the Meso-tidal Changjiang Estuary     

M-A. Sicre  I. Broyelle  A. Lorre  A. Saliot 《Estuarine, Coastal and Shelf Science》1993,37(6)

n-Alkanes and polyaromatic hydrocarbons (PAHs) were analysed on suspended particles from surface waters of the Changjiang Estuary to assess the sources and fate of river-borne material in a meso-tidal riverine system. The n -alkane and PAH assemblages indicated prevailing terrestrial and anthropogenic inputs. Measurements performed at several stations within the estuary showed lower concentrations in the North than in the South Channel. These observations were in agreement with the dynamics and flow pattern of the Changjiang in this part of the estuary. Concentrations measured at a tidal series station over two tidal cycles exhibited a significant increase in flooding of more saline waters. Total suspended particles were also higher, reaching their maximum value (1·9 g l^-1) at high tide during the first flood. These findings were attributed to the landwards transport of the turbidity maximum zone from the outer estuary, as the Taiwan Warm Current funnels into the Changjiang River mouth. Saltier and less turbid waters with a more pronounced marine character could reach the tidal series site at the final stage of the second flood. During the ebb, suspended n-alkane and PAH concentrations were lower but their compositional features remained similar to those during the flood. A high total suspended particle concentration was observed during the ebb, presumably due to the Huang Pu waters flushing. The n -alkane and PAH content of the particles during such an event pointed out stronger contamination of the waters after crossing the highly populated and industrialized area of Shanghai. Flux calculations based on current meter data indicated significant differences between flood and ebb transports.  相似文献   

Retrospective analysis: bile hydrocarbons and histopathology of demersal rockfish in Prince William Sound,Alaska, after the Exxon Valdez oil spill     

Marty GD  Hoffmann A  Okihiro MS  Hepler K  Hanes D 《Marine environmental research》2003,56(5):569-584

Demersal rockfish are the only fish species that have been found dead in significant numbers after major oil spills, but the link between oil exposure and effect has not been well established. After the 1989 Exxon Valdez oil spill in Prince William Sound, Alaska, several species of rockfish (Sebastes spp.) from oiled and reference sites were analyzed for hydrocarbon metabolites in bile (1989-1991) and for microscopic lesions (1990 and 1991). Biliary hydrocarbons consistent with exposure to Exxon Valdez oil were elevated in 1989, but not in 1990 or 1991. Significant microscopic findings included pigmented macrophage aggregates and hepatic megalocytosis, fibrosis, and lipid accumulation. Site differences in microscopic findings were significant with respect to previous oil exposure in 1991 (P=0.038), but not in 1990. However, differences in microscopic findings were highly significant with respect to age and species in both years (P<0.001). We conclude that demersal rockfish were exposed to Exxon Valdez oil in 1989, but differences in microscopic changes in 1990 and 1991 were related more to age and species differences than to previous oil exposure.  相似文献   

The North Cape oil spill: hydrocarbons in Rhode Island coastal waters and Point Judith Pond.     

C M Reddy  J G Quinn 《Marine environmental research》2001,52(5):445-461

On 19 January 1996, the North Cape oil barge ran aground near Moonstone Beach, RI, and spilled over 2700 metric tons of No. 2 fuel oil during a severe winter storm. High winds and rough seas drove the oil into the water column, and the oil spread throughout Block Island Sound and into several coastal salt ponds. Over 50 water samples were collected from Point Judith Pond (PJP) and the southern coast of Rhode Island for four months after the spill and analyzed for polycyclic aromatic hydrocarbons (PAHs) and total petroleum hydrocarbons (TPHs). These analyses revealed that at least 60 km2 of coastal waters were impacted from the spill. Maximum concentrations of sigmaPAHs and TPHs were 115 and 3940 microg l(-1), respectively. The percentage of sigmaPAHs relative to the TPHs for all samples varied from 0.2 to 43%, showing that there was no clear relationship between sigmaPAHs and TPHs for the whole dataset and likely resulting from spatial and temporal partitioning over the course of the spill. However, within the dataset, there were stronger correlations for distinct samples collected at similar locations and times. In PJP, water column concentrations of individual PAHs decreased at rates of 0.08-0.24 day(-1) and lower-molecular weight PAHs were removed faster than higher-molecular weight PAHs.  相似文献   

广东沿海近江牡蛎氯代烃和石油烃含量分布与变化趋势   总被引：5，自引：0，他引：5  

甘居利  林钦  蔡文贵  贾晓平 《热带海洋学报》2006,25(1):47-50

根据历史调查资料和近年的观测数据,比较了广东沿海近江牡蛎Crassostrearivularis体中氯代烃和石油烃含量的地理分布与时间变化。2003年牡蛎体中六六六、滴滴涕、多氯联苯平均含量(湿重)分别为0.469、3.40和45.1ng·g-1,地理分布为粤东岸段>粤西岸段>珠江口。1989年以来六六六、多氯联苯含量呈持续下降趋势,滴滴涕含量在1989—1993年呈下降趋势,但在2003年明显反弹。牡蛎体中石油烃年平均含量1989年以来有一定的波动,2003年为4.75μg·g-1(湿重,大港原油当量),地理分布为珠江口>粤东岸段>粤西岸段。  相似文献   

Hydrocarbon evolution for a north-south section of the South Caspian Basin     

E. Bagirov  R. Nadirov  I. Lerche 《Marine and Petroleum Geology》1997,14(7-8)

A 150 km length, 6-second deep, seismic line across the west central and north parts of the South Caspian Basin was used to construct quantitative dynamical, thermal and hydrocarbon evolution patterns. The depth of the west part of the 2-D section of the South Caspian Basin is almost 30 km. The computer program GEOPETII was used to provide quantitative evolution models. The procedure provided an opportunity to investigate the development dynamics of: excess fluid pressure, porosity retention, rock fracturing, compaction, heat transfer, maturity, generation pressure, kinetic hydrocarbon generation, migration and accumulation, together with solubility effects on hydrocarbon transport. The results suggest that: (i) Temperature is 350–400°C in the deepest part of the section at a depth of 26–29 km; (ii) The highest values of excess pressure nearly twice hydrostatic fluid pressure are in Jurassic and Cretaceous formations in the west part of the section, which has now subsided to a depth of about 20–27 km; (iii) Major oil and gas generation began in the last 10-5 MYBP, the migration in free-phase and in water solution occurring dominantly in the last few million years; (iv) Trapping of hydrocarbons took place mainly, but not exclusively, in the 3–9 km depth interval in the sands of the Productive Series of the Pilocene, embedded in a shale sequence; (v) Oil and gas filling of the shallow reservoirs by oil and gas is on-going today, indicating an extremely high productivity for any reservoir found in the offshore area; (vi) There is overlap with depth of oil and gas reservoirs, and the total amount of hydrocarbons estimated to be trapped is considerable; (vii) The high overpressure expected makes for a drilling hazard, but one which it is worthwhile to overcome if the anticipated oil and gas accumulations are encountered.  相似文献