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 15 毫秒
1.
The distributions of hydrocarbons in sediment cores dated by 210Pb (1845–1977) from San Pedro and San Nicolas Basins in the Southern California Bight have been determined by gas Chromatographic and combined gas chromatographic-mass spectrometric analysis. The chromatograms of the hydrocarbons contain peaks of resolved alkanes and cycloalkanes, as well as an unresolved complex mixture which decrease in content with increasing depth in both of the cores. The concentrations of o,p' andp,p'-DDE are highest in the top 50 mm of the San Pedro core section. The 45–50 mm segment of this core was deposited in the 1945–1950 period when DDT (the precursor of DDE compounds) came into common use. The relatively high content of hydrocarbons and DDE in this core is attributable to the proximity of the site to the San Pedro Harbor which receives petroleum residues from shipping, sewage outfalls and industrial effluents. The presence of only traces of DDE throughout the San Nicolas core, and the low hydrocarbon content are explainable by the greater distance of this basin from anthropogenic inputs and probably a greater rate of degradation of deposited organic matter during bioturbation. δ13C, δ15N and electron-spin resonance analyses of kerogens and humic substances in these cores, indicate that most of this organic matter in these sediments is of a marine origin.  相似文献   

2.
The burial characteristics and toxicity risks associated with n-alkanes and polycyclic aromatic hydrocarbons (PAHs) in the riverine and estuarine sediments of the Daliao River watershed were investigated based on three sediment cores. The sum of the n-alkane and PAH concentrations, normalized to organic carbon (OC), ranged from 0.27 to 63.09 μg g?1OC?1 and 6.60 to 366.20 μg g?1OC?1, respectively. The features and the history of industrial activities, such as the oil and chemical industries and port activities near the river and estuary, resulted in different distributions and sources of hydrocarbons. The sources of pollution were identified based on n-alkane indexes and on diagnostic ratios of PAHs. The diagnostic ratios indicated that the n-alkanes were derived from both biogenic and petrogenic sources in different proportions and that the PAHs were derived primarily from petrogenic combustion sources. A hierarchical cluster analysis grouped the core samples into two clusters. The first cluster, river sediments, corresponded to industrial activities; the second cluster, estuarine sediments, corresponded to port shipping activities. The toxic potency of the PAHs in the cores was assessed in terms of toxic equivalents (TEQs) of dibenzo[a,h]anthracene and benzo[a]pyrene. The top layer of the sediment in the cores had a relatively high toxicity. The TEQ values for benzo(a)pyrene (TEQBaP) and dioxins (TEQTCDD) furnished a consistent assessment of the PAHs in the sediment cores.  相似文献   

3.
《Applied Geochemistry》1998,13(3):293-304
Distributions of 15 elements with depth in two sediment cores from Puck Bay in the Gulf of Gdansk show that Ag, Cd, Pb, Zn and possibly Cu and Ni are anthropogenically enriched in the sediments there. The concentrations of these elements decrease sharply with depth in the sediment column and the elements are preferentially enriched in the <2 μm size fraction of the sediment. The sequence of element enrichment depends on whether the enrichment factor (EF) and the anthropogenic factor (AF) are used to calculate the element enrichment. By contrast, the anthropogenic elements show no systematic decrease in concentration with depth in a sediment core taken from near the mouth of the Vistula River. This reflects the higher sedimentation rate there such that the entire upper 20 cm of the core was deposited during the major, post-war period of industrialization in Poland. In addition, these elements are enriched in the 2–63 μm fraction compared to the <2 μm fraction in these sediments. This suggests that the heavy metals are mainly adsorbed on Fe oxyhydroxide particles with diameters greater than 2 μm at the hydrological front where Vistula river water mixes with brackish Baltic water. It appears that heavy-metal pollution of sediments in parts of Puck Bay may be greater than that near the mouth of the Vistula River which may reflect, in part, the higher sedimentation rate near the mouth of the Vistula River. The mode of incorporation of heavy-metals into the sediments in the two areas may also be different.  相似文献   

4.
The Tunisian environmental legislation that follows the EC Directives requires monitoring of persistent, toxic and bio-accumulated substances commonly considered as hazardous substances. In order to comply with this requirement, samples of sea water, sediment and biota from the urbanized and industrialized coast line of Sfax city are investigated. This study presents the results of petroleum hydrocarbon content, distribution and probable origin (anthropogenic and/or biogenic) in 16 intertidal sediments of Sfax coastal area. Alkane distribution indices and hydrocarbon distribution patterns are used to identify natural and anthropogenic input. Non-aromatic hydrocarbons present a high concentration with a range varying from 180 to 1,400 μg/g of dry sediment. The total concentrations of polycyclic aromatic hydrocarbons (PAHs) varied from 0.41 to 5.6 μg/g dry weight. These concentrations are comparable to other marine areas that receive important inputs. n-Alkanes with carbon number ranging from 15 to 35 are identified to be derived from both biogenic and anthropogenic sources in varying proportions. Pristane/phytane ratio shows values lower than 1.4 suggesting the presence of petroleum contamination. This is confirmed by the presence of a large group of unresolved complex mixture and the identification of hopanes with predominant C29 and C30 compounds and steranes with predominance of C27 over C28 and C29 compounds. Ratios of selected PAH concentrations indicate petrogenic and pyrolytic origin of hydrocarbons. Anthropogenic hydrocarbon inputs were more apparent at sites associated with industrial discharges, shipping activities and sewage outfalls.  相似文献   

5.
The distributions of a series of structurally related C25 and C30 biogenic alkenes in sediments of the Narragansett Bay estuary have been determined. The suite of alkenes detected differs both quantitatively and qualitatively from those previously reported in other estuanne and coastal regions. Four C25 mono- and dienes and one C30 diene comprise 73–91% of the total alkenes in all surface (upper 2.5–5 cm) sediments analyzed. However, significant geographic variations exist in the relative abundance of these five compounds throughout the estuary. A comparison of alkene concentrations with δ13C of the bulk sedimentary organic matter has shown that the geographic variations of some alkenes reflect the distribution of marine organic matter, suggesting a marine source for these compounds. The distributions of other alkenes are not similarly correlated. In particular, concentrations of the C30 diene are relatively constant and exhibit no dependence on the origin of organic matter in these sediments. This distribution implies an in situ production of this alkene throughout the estuary. Analysis of several sediment cores reveals that alkene concentrations are generally highest at the surface and decrease to low, constant values within the upper 25 cm. An exception is the subsurface concentration of one C25 diene, which exhibits an increase at the same depth in two separate upper bay cores.  相似文献   

6.
Sediment cores from two locations in Green Bay and two in lake Michigan were analyzed for 12 polycyclic aromatic hydrocarbons (PAHs), loss-on-ignition (LOI),210Pb,137Cs, and7Be to study differences in deposition patterns between the freshwater estuary Green Bay, with several local sources, and the open Lake Michigan, dominated by atmospheric inputs. We found that the remote sites receive relatively less high-molecular weight PAHs such as ideno(1,2,3-cd)pyrene and dibenz(ah)anthracene and are more depleted in anthracene and pyrene. This may be related to a low Henry’s law constant for the high molecular compounds and to selective photo-oxidation of anthracene and pyrene during transport. While sedimentation rates are higher in Green Bay than in the open lake, the PAH levels are generally comparable (0.3–8.5 μg g?1) in the two areas. However, the highest PAH levels are found in a core from Green Bay (GB88G). The two Green Bay cores have total PAH concentration maxima in 1985, which appear to be related to the combustion of petroleum. Also, one Green Bay core (GB88G) and the two from Lake Michigan exhibit PAH maxima in the early 1950s in agreement with observations from other study areas. There is a significant correlation between total PAH and LOI, and thus total organic carbon, for the Green Bay cores, but little or no such correlation for the Lake Michigan cores. This may indicate that PAHs in Green Bay are effectively scavenged by settling detritus.  相似文献   

7.
Weather and water-quality data from 1980 to 1989 were correlated with fluctuations in submersed macrophyte populations in the tidal Potomac River near Washington, D.C., to elucidate causal relationships and explain population dynamics. Both reaches were unvegetated in 1980 when mean growing-season Secchi depths were <0.60 m. Macrophyte resurgence in the upper tidal river in 1983 was associated with a growing-season Secchi depth of 0.86 m, total suspended solids (TSS) of 17.7 mg l?1, chlorophyll a concentrations of 15.2 μg l?1, significantly higher than average percent available sunshine, and significantly lower than average wind speed. From 1983 to 1989, mean seasonal Secchi depths <0.65 m were associated with decrease in plant coverage and mean seasonal Secchi depths >0.65 were associated with increases in plant coverage. Changes in mean seasonal Secchi depth were related to changes in mean seasonal TSS and chlorophyll a concentration; mean Secchi depths >0.65 generally occur when seasonal mean TSS is <19 mg l?1 and seasonal mean chlorophyll a concentration is ≤15 μg l?1. Secchi depth is highly correlated with plant growth in the upper tidal river and chlorophyll a and TSS with plant growth in the lower tidal river. Wind speed is an important influence on plant growth in both reaches.  相似文献   

8.
  相似文献   

9.
《Applied Geochemistry》2000,15(4):425-438
The dissolution of silica and diffusion of reactive dissolved Si in the porewaters of river sediments are investigated using sediments of different physical and chemical properties. Three sediments are considered: (a) from sectioned cores taken from a river-bed, (b) fine organic-rich surface sediment (<5 cm depth) installed in a fluvarium channel and, (c) coarse river sediment of low organic matter content also installed in a fluvarium channel. Dissolution rates of silica are measured at 10°C using batches of suspended material. The derived dissolution rate constants show large differences between the sediments. The river bed-sediment cores had vertical concentration profiles of dissolved Si that are consistent with the diffusion and dissolution of biogenic silica. Experiments in a fluvarium channel enabled Si fluxes to be calculated from a mass-balance of the overlying solution. The results are consistent with the attainment of a steady-state concentration profile of dissolved Si in the sediment. There are no discernible effects of water velocity over the sediment between 5 and 11 cm s−1. However, at 20 cm s−1, the flux increases as a result of either entrainment of fine particles at the surface or advective effects in the surface sediment. A fluvarium experiment with the fine sediment (<125 μm) over 61 days, produced a concentration profile with the highest concentration of 1025 μmol dm−3 at a depth of 4–5 cm in the sediment. A FORTRAN program is used to model the results of the increase in dissolved Si in the overlying water and development of a concentration profile in the porewater. This leads to a sediment diffusion coefficient of 1.21×10−9 m2 s−1 at 8.8°C at the beginning of the experiment and rate constant k=13.1×10−7 s−1 at pH=7.82 and average temperature of 7.6°C for the entire experiment. Fluxes measured at the sediment–surface interface and calculated assuming steady-state profiles had developed are typically 0.01–0.04 μmol m−2 (of river bed) s−1. The approach enables the efflux of dissolved Si from bottom-sediments to be estimated from dissolution rates measured using suspensions of bed-sediment.  相似文献   

10.
In order to test the assumption that accretion rates of intertidal salt marshes are approximately equal to rates of sea-level rise along the Rhode Island coast,210Pb analyses were carried out and accretion rates calculated using constant flux and constant activity models applied to sediment cores collected from lowSpartina alterniflora marshes at four sites from the head to the mouth of Narragansett Bay. A core was also collected from a highSpartina patens marsh at one site. Additional low marsh cores from a tidal river entering the bay and a coastal lagoon on Block Island Sound were also analyzed. Accretion rates for all cores were also calculated from copper concentration data assuming that anthropogenic copper increases began at all sites between 1865 and 1885. Bulk density and weight-loss-on-ignition of the sediments were measured in order to assess the relative importance of inorganic and organic accumulation. During the past 60 yr, accretion rates at the eight low marsh sites averaged 0.43±0.13 cm yr?1 (0.25 to 0.60 cm yr?1) based on the constant flux model, 0.40±0.15 cm yr?1 (0.15 to 0.58 cm yr?1) based on the constant activity model, and 0.44±0.11 cm yr?1 (0.30 to 0.59 cm yr?1) based on copper concentration data, with no apparent trend down-bay. High marsh rates were 0.24±0.02 (constant flux), 0.25±0.01 (constant activity), and 0.47±0.04 (copper concentration data). The cores showing closest agreement between the three methods are those for which the excess210Pb inventories are consistent with atmospheric inputs. These rates compare to a tide gauge record from the mouth of the bay that shows an average sea-level rise of 0.26±0.02 cm yr?1 from 1931 to 1986. Low marshes in this area appear to accrete at rates 1.5–1.7 times greater than local relative sea-level rise, while the high marsh accretion rate is equal to the rise in sea level. The variability among the low marsh sites suggests that marshes may not be poised at mean water level to within better than ±several cm on time scales of decades. Inorganic and organic dry solids each contributed about 9% by volume to low marsh accretion, while organic dry solids contributed 11% and inorganic 4% to high marsh accretion. Water/pore space accounted for the majority of accretion in both low and high marshes. If water associated with the organic component is considered, organic matter accounts for an average of 91% of low marsh and 96% of high marsh accretion. A dramatic increase in the organic content at a depth of 60 to 90 cm in the cores from Narragansett Bay appears to mark the start of marsh development on prograding sand flats.  相似文献   

11.
The biodegradability of polycyclic aromatic hydrocarbons such as naphthalene, fluorene, anthracene and phenanthrene by a halotolerant bacterial consortium isolated from marine environment was investigated. The polycyclic aromatic hydrocarbons degrading bacterial consortium was enriched from mixture saline water samples collected from Chennai (Port of Chennai, salt pan), India. The consortium potently degraded polycyclic aromatic hydrocarbons (> 95%) at 30g/L of sodium chloride concentration in 4 days. The consortium was able to degrade 39 to 45% of different polycyclic hydrocarbons at 60 g/L NaCl concentration. Due to increase in salinity, the percent degradation decreased. To enhance polycyclic aromatic hydrocarbons degradation, yeast extract was added as an additional substrate at 60g/L NaCl concentration. After the addition of yeast extract, the consortium degraded > 74 % of polycyclic aromatic hydrocarbons at 60 g/L NaCl concentration in 4 days. The consortium was also able to degrade PAHs at different concentrations (5, 10, 20, 50 and 100 ppm) with 30 g/L of NaCl concentration. The polycyclic aromatic hydrocarbons degrading halotolerant bacterial consortium consists of three bacterial strains, namely Ochrobactrum sp., Enterobacter cloacae and Stenotrophomonas maltophilia.  相似文献   

12.
Estuaries located in the northern Gulf of Mexico are expected to experience reduced river discharge due to increasing demand for freshwater and predicted periods of declining precipitation. Changes in freshwater and nutrient input might impact estuarine higher trophic level productivity through changes in phytoplankton quantity and quality. Phytoplankton biomass and composition were examined in Apalachicola Bay, Florida during two summers of contrasting river discharge. The <20 μm autotrophs were the main component (92?±?3 %; n?=?14) of phytoplankton biomass in lower (<25 psu) salinity waters. In these lower salinity waters containing higher dissolved inorganic nutrients, phycocyanin containing cyanobacteria made the greatest contribution to phytoplankton biomass (69?±?3 %; n?=?14) followed by <20 μm eukaryotes (19?±?1 %; n?=?14), and phycoerythrin containing cyanobacteria (4?±?1 %; n?=?14). In waters with salinity from 25 to 35 psu that were located within or in close proximity to the estuary, >20 μm diatoms were an increasingly (20 to 70 %) larger component of phytoplankton biomass. Lower summer river discharges that lead to an areal contraction of lower (5–25 psu) salinity waters composed of higher phytoplankton biomass dominated by small (<20 μm) autotrophs will lead to a concomitant areal expansion of higher (>25 psu) salinity waters composed of relatively lower phytoplankton biomass and a higher percent contribution by >20 μm diatoms. A reduction in summer river discharge that leads to such a change in quantity and quality of estuarine phytoplankton available will result in a reduction in estuarine zooplankton productivity and possibly the productivity of higher trophic levels.  相似文献   

13.
This study aimed to evaluate the total concentration of polycyclic aromatic hydrocarbons in sediments of Iguassu River in Southern Brazil. Alongside the concentration, the amount of such compounds bioavailable was also evaluated. This is accomplished by comparing its total amount present in sediments and the amount extracted by n-butanol. The results showed that the total concentration of polycyclic aromatic hydrocarbons presented in sediment ranged from 4.49 to 58.75???g/g. The total amount of polycyclic aromatic hydrocarbons extracted by n-butanol ranged from 1.22 to 17.07???g/g. The use of n-butanol represents the mimetic conditions that hydrocarbons, derived from oil, could be taken up by organisms. Most of the hydrocarbons extracted by n-butanol were those with lower octanol?Cwater partition constant, usually those with three and four rings. Compounds with more than four rings were extracted in lower or insignificant amounts. Even the hydrocarbons with lower molecular weight available may be degraded or eliminated by organisms, when accumulated. Estimating bioavailability of hydrocarbons represents what specific hydrocarbons could be available to be taken up by organisms.  相似文献   

14.
Aluminium has received great attention in the second half of the 20th century, mainly in the context of the acid rain problem mostly in forest soils. In this research the effect of land use and depth of the groundwater on Al, pH and DOC concentration in groundwater under Dutch sandy soils has been studied. Both pH and DOC concentration play a major role in the speciation of Al in solution. Furthermore, the equilibrium with mineral phases like gibbsite, amorphous Al(OH)3 and imogolite, has been considered. Agricultural and natural land use were expected to have different effects on the pH and DOC concentration, which in turn could influence the total Al concentration and the speciation of Al in groundwater at different depths (phreatic, shallow and deep). An extensive dataset (n = 2181) from the national and some provincial monitoring networks on soil and groundwater quality was used. Land use type and groundwater depth did influence the pH, and Al and DOC concentrations in groundwater samples. The Al concentration ranged from <0.4 μmol L−1 at pH > 7 to 1941 μmol L−1 at pH < 4; highest Al concentrations were found for natural-phreatic groundwater. The DOC concentration decreased and the median pH increased with depth of the groundwater. Natural-phreatic groundwater showed lower pH than the agricultural-phreatic groundwater. Highest DOC concentrations were found for the agricultural-phreatic groundwater, induced by the application of organic fertilizers. Besides inorganic complexation, the NICA-Donnan model was used to calculate Al3+ concentrations for complexation with DOC. Below pH 4.5 groundwater samples were mainly in disequilibrium with a mineral phase. This disequilibrium is considered to be the result of kinetic constraints or equilibrium with organic matter. Log K values were derived by linear regression and were close to theoretical values for Al(OH)3 minerals (e.g. gibbsite or amorphous Al(OH)3), except for natural-phreatic groundwater for which lower log K values were found. Complexation of Al with DOC is shown to be an important factor for the Al concentrations, especially at high DOC concentrations as was found for agricultural-phreatic groundwater.  相似文献   

15.
This study investigates the extent of post-depositional alteration of δD values of n-alkyl lipids, isoprenoids, and kerogen isolated from a continuous 450 m core that covers the transition from thermally immature to early mature sediments in the lacustrine Kissenda Formation, Lower Cretaceous, Gabon Basin. Large variations in δD values (up to 40‰ for nC17 and up to 30‰ for nC29 alkanes as well as up to 10‰ for kerogen) in closely spaced samples are evident throughout the core and remain preserved even at the bottom of the section. δD values of individual n-alkanes show a slight overall D-enrichment with depth, and a general trend of increasing δD values with increasing n-alkane chain length characterizes all samples, particularly in those below 600 m depth. Hydrogen isotopic compositions of kerogen samples overlap with those of n-alkanes throughout the section. δD values of pristane and phytane are more negative than those of nC17 alkane by as much as 120‰ at shallow depths but increase dramatically and approach δD values of nC17 alkane in the samples closest to the oil window. Integration of analytical and computational results indicates that: (1) n-alkanes and isoprenoids have the potential to preserve the original biological signal before the onset of oil generation; (2) isomeric and structural rearrangements taking place at the beginning stages of oil generation do not influence significantly the δD values of n-alkanes and kerogen. However, these processes have a major effect on the isotopic composition of isoprenoids, causing isotopic D-enrichment up to 90‰.  相似文献   

16.
The concentrations and isotopic compositions of the various forms of nitrogen in silty clay sediments from the Bay of Quinte (Lake Ontario) have been determined. The total organic-N content is high throughout the sediment profiles and generally decreases with depth. On the contrary, exchangeable NH+4-N concentration is quite low and tends to increase with depth in two out of three sediment cores examined. The concentration of non-exchangeable NH+4-N and the 6 N HCl hydrolyzable NH+4-N are relatively constant with depth. Among the N fractions analyzed, the exchangeable NH+4-is most enriched in 15N. In most cases, the δ 15 N values of the N fractions remain relatively constant with sediment depth. There is no apparent correlation of δ 15 N values with the N concentration for any of the individual N fractions. The observed ranges in the δ 15 N values are: exchangeable NH+4, + 5–+10‰; 6 N HCl hydrolyzable total N and 6 N HCl hydrolyzable NH+4-N, + 3.5–+5.5‰.  相似文献   

17.
Aliphatic and aromatic hydrocarbons in sediments of the middle and lower Mississippi Fan and two intraslope basins in the Gulf of Mexico are derived from terrestrial organic matter and thermogenic, mature hydrocarbons. The terrestrial hydrocarbon component consists primarily of terrigenous, plant biowaxes (n-alkanes with 21 to 33 carbons). The occurrence of thermogenic hydrocarbons in immature near-surface sediments, their molecular distributions and concentration variations with depth suggest that the majority of these mature hydrocarbons have migrated from a source much deeper in the sediment column. A portion of the thermogenic hydrocarbons may be derived from recycled material and includes phenanthrene, methyl phenanthrenes, chrysene and benzopyrenes. The migrated, thermogenic hydrocarbons include normal and isoprenoid alkanes with less than 21 carbons, naphthalene, methyl naphthalenes, ethyl naphthalenes and other aromatics of similar volatility (i.e., biphenyl, acenaphthene and fluorene). Triterpane, sterane and aromatized sterane distributions suggest that the thermogenic hydrocarbons at both sites have a common source and are overprinted with immature sediment hydrocarbons. The biomarker distributions and carbon isotopic compositions of the thermogenic hydrocarbons are atypical for petroleum produced in the Gulf of Mexico. Molecular distributions of the hydrocarbons are constant, regardless of the present depth of occurrence, suggesting that they have migrated in a separate phase. The upward migration of hydrocarbons from deeper sources is a wide-spread phenomenon in the Gulf of Mexico with several documented cases of massive seepage (visible oil) as well as the more diffuse permeation of Pleistocene sediments of the Mississippi Fan and two intraslopes reported here.  相似文献   

18.
Aliphatic hydrocarbon compositions were quantitatively characterized in plankton, sediment trap-collected particulate materials and sediments from Dabob Bay using high resolution glass capillary gas chromatography. The average net accumulation of individual hydrocarbons measured in a 1-yr series of sediment traps was compared with the net accumulation of corresponding compounds measured in three depth intervals of 210Pb-dated bottom sediments. Systematic and rapid decreases in the net accumulation of individual hydrocarbons were observed from the sediment traps to the sediments. Most pronounced decreases were measured for planktonically derived hydrocarbon constituents (e.g. pristane and two unsaturated compounds) which are rapidly remineralized at or near the sediment-water interface. Consequently, the amount of each compound measured in deposited sediments is not necessarily a quantitative indication of its initial flux to the sediments. The n-alkanes (C25,27,29,31). characteristic of terrestrial plant waxes, are the predominant hydrocarbons measured by 4–6 cm depth in these sediments and show reasonably constant net accumulation below this interval.Significant diagenetic alteration of the bulk organic matter contained in the average sediment trap particulate material is also noted through comparison with bottom sediments on the basis of organic C/N and δ13C measurements. Organic matter elementally similar to marine plankton is preferentially remineralized upon deposition of the sedimentary particulates. The residual organic matter remaining and buried in the bottom sediments closely resembles terrestrial organic matter.  相似文献   

19.
This work reports the historical trends and sources of aliphatic hydrocarbons (AHs) and polycyclic aromatic hydrocarbons (PAHs) in two 210Pb dated sediment cores extracted from the central mud areas of Bohai Sea (Bohai). The TOC/TN ratio of the bulk organic matter (OM) and the composition of the n-alkanes suggest that the sedimentary organic matter was of mixed marine and terrigenous sources. The coarser sediment grain size and decreasing C/N ratios since ∼1976 could be attributed to the relocation of the Yellow River mouth causing a decreased influence of Yellow River derived sediments and associated OM into the central Bohai. The concentration of total 16 PAHs in the two cores ranged from 34.2-202 ng/g (mean, 91.5) for BC1, and from 53.3-186 ng/g (mean, 103) for BC2, with a high abundance of 2-3 ring PAHs. Perylene in the two cores mainly originated from terrigenous sources via riverine discharge and thus could be potentially related to changes in the sediment load from the Yellow River into the Bohai over time. Petroleum inputs could be revealed by ratios of methylphenanthrenes to phenanthrene (MP/P) and the patterns of more stable geochemical biomarkers (hopanes and steranes) along the two cores, in addition to the presence of unresolved complex mixtures (UCM) in the surface layers. Source diagnostic ratios of PAHs indicated a pyrogenic origin from biomass and coal combustion with a minor petroleum contribution. Downcore trends of compositional PAHs profiles were in agreement with the socio-economic development in China in the past decades. This temporal variation of sedimentary PAHs can also reflect a different evolution stage of energy structure in China as compared with those of the western developed countries.  相似文献   

20.
The dissolution kinetics of shallow water marine carbonates (low-Mg calcite, aragonite and Mg-calcites) were investigated in seawater (S = 35) at 25°C and a PCO2 of 10?2.5 atm. using the pH-stat method. Carbonate dissoluton rates (μmoles g?1 hr?1) fit the empirical kinetic expression, R = k(1 - Ω)n, where R = dissolution rate, k = rate constant, Ω = saturation state, and n = order of reaction. Reaction orders were near 2.9 for low-Mg calcites, 2.5 for aragonites and 3.4 for Mg-calcites.The rate constant, k, expressed as μmoles g?1 hr?1, varied by nearly a factor of ten for the different samples, reflecting differences in amount of reactive surface area. Reactive surface area of the biogenic phases ranged from 0.3% to 66% of the total surface area determined by the BET gas adsorption method. The discrepancy between reactive and total surface area was greatest for samples with high BET surface areas (> 1 m2 g?1) and delicate microstructures.Relative dissolution rates of the various biogenic carbonates as a function of seawater calcium carbonate ion molal product (IMP) were related to both mineral stability and grain microstructure. In seawater undersaturated with respect to aragonite, finely crystalline aragonites dissolved more rapidly than thermodynamically less stable high Mg-calcites (15–18 mole% MgCO3) with lower reactive surface areas. Therefore, under certain conditions, differences in grain microstructural complexity can override thermodynamic constraints and lead to selective dissolution of a thermodynamically more stable mineral phase.  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