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1.
Polycyclic aromatic hydrocarbon (PAH) compositions were determined in plankton, sediment-trap-collected particulate material and sediment cores from Dabob Bay using a high performance liquid Chromatographie (HPLC)/fluorescence technique. The annual flux of individual PAH measured in a series of sediment traps was compared with the flux of corresponding compounds determined from 210Pb dated bottom sediments. Systematic seasonal variations in the fluxes and concentrations of PAH, Al and organic carbon in the trap-collected particulates and seasonally collected plankton were also investigated to determine whether or not PAH are associated with either terrestrial or marine-derived materials.Concentrations of all PAH studied increased tenfold within the last 80–100 yr of sediment deposition, except for perylene which displayed a reasonably constant concentration profile. This suggests at least two sources contribute to the observed sedimentary PAH compositions in Dabob Bay, i.e., anthropogenic combustion and a natural source. Plankton and sediment trap-collected particulates contained PAH mixtures qualitatively similar to underlying surface sediments. Microscopic examination indicated fecal pellets were the major form of particulate material in the sediment traps. The fecal pellets collected in the sediment trap time series quantitatively account for essentially 100% of the PAH fluxes measured in the 210Pb dated sediments, implying Zooplankton fecal pellets control the removal of PAH to Dabob Bay sediments. These measurements provide clear evidence that the PAH studied are not produced after sediment deposition. The observed seasonal covariations of PAH and Al in both sediment trap and plankton samples further indicate that PAH originate from terrestrially-based sources, are introduced into the marine environment by runoff and erosion or atmospheric deposition and are not produced by marine plankton.  相似文献   

2.
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   

3.
Although recent research has indicated that bacteria may contribute an important fraction of biochemical residues in terrestrial and marine environments, it is difficult for geochemists to identify contributions from these ubiquitous and biochemically diverse organisms. Previous studies have suggested uronic acids and O-methyl sugars may be useful indicators of microbial abundance and activity, but have been limited primarily to analyses of a small number of isolated samples. We report here comparative distributions of O-methyl sugars, uronic acids, and aldoses in sediment trap material and sediments from Dabob Bay, WA and nearby Saanich Inlet, BC, where temporal and spatial trends may be used together with well-established patterns in other biochemicals to identify bacterial contributions against the background of other carbohydrate sources.O-methyl sugars and uronic acids were important contributors to the overall flux and burial of polysaccharide material in Dabob Bay and Saanich Inlet, composing ≤12 wt% of the total carbohydrate yields from sediment trap and sediment samples. O-methyl sugars accounted for an average of 5% of the carbohydrate yields from sediment trap materials and sediments, but were found rarely and only in low abundance in vascular plant tissues, phytoplankton, and kelp. In contrast, uronic acids were abundant products of sediment trap material and sediments, as well as vascular plant tissues, where in some cases they predominated among all carbohydrates. Uronic acid abundance in sediment trap material averaged 3% and ranged to >6% of total carbohydrate yields.The persistence of total minor sugar yields in water column collections from Dabob Bay throughout the seasonal cycle indicated they had a primary source that was not directly related to plankton bloom cycles nor pulsed inputs of vascular plant remains. Subsurface maxima in total minor sugar yields (and several individual components) within sediment cores from both sites indicate in situ sedimentary sources. Taken together, the observed environmental distributions strongly suggest that the minor sugar abundances in Dabob Bay and Saanich Inlet were controlled by in situ microbial production.  相似文献   

4.
The distribution of isoprenoid and branched glycerol dialkyl glycerol tetraether (GDGT) lipids was studied in material from various sources in and around Lake Challa, a crater lake on the southeastern slope of Mt. Kilimanjaro (Tanzania), to examine the provenance of GDGTs in lake sediments and their potential application as palaeoenvironmental and palaeoclimatic proxies. The study material included samples collected at monthly intervals in a sediment trap over one complete annual cycle, particles suspended in the stratified water column, profundal surface sediments, and soils surrounding the lake. The sediment trap time series revealed that crenarchaeol and related isoprenoid GDGTs were predominantly produced in January and February, following the locally prominent short rain season (November-December). The TEX86-inferred temperature derived from sedimenting particles corresponded well with lake surface-water temperature at this time of largest crenarchaeol flux. Molecular ecological analysis showed that Group 1.1a and 1.1b crenarchaeota are the most likely source organisms of these GDGTs. GDGT-0 in the lake sediments does not only originate from lake surface-dwelling crenarchaeota but seems predominantly derived from archaea residing in the deeper, anoxic part of the water column. The main flux of branched GDGTs to the sediment was during the short rain season and is most probably derived from eroded catchment soils in surface run-off. However, a contribution from in-situ production of branched GDGTs in the lake sediment or water, or in groundwater cannot be fully excluded. We conclude that palaeoclimatic reconstruction based on branched GDGT distributions in lake sediments should only be performed when the origin of those branched GDGTs is well constrained.  相似文献   

5.
近海油气藏渗漏烃的检测方法综述   总被引：7，自引：0，他引：7  
主要总结了海域油气藏渗漏烃的航空遥感和地球化学检测方法.遥感测量可以从宏观上圈定海面油膜的分布范围,是海上油气藏勘探前期常用的廉价方法;海底沉积物取芯测量和海水嗅探器现场分析是海域油气藏渗漏烃地球化学检测的主要手段,海水样品的脱气处理是海水介质中渗漏烃地球化学检测的关键环节;海水和海底沉积物取样设备与脱气技术的不断完善,为海域油气藏渗漏烃的检测提供了基本保障;目前,底层水采样分析与海底沉积物取芯分析已成为一种有效且相对经济的海域油气藏渗漏烃检测技术组合,与一些地球物理方法结合应用,可有效地圈定海底下方渗漏源的位置.  相似文献   

6.
Concentrations of dissolved nitrate, silicate, and phosphate in water flooding intertidal sediments at Pecks Cove and along the axis of Cumberland Basin, Bay of Fundy were measured throughout the year. Exchanges of dissolved nutrients between intertidal sediments and overlying water were measured by enclosing water in chambers over undisturbed sediment. Nitrate concentrations in the water usually decreased during incubations while silicate was released by sediments during summer and consumed during fall. Particles which settled in sediment traps exposed during periods of high tide were stirred in filtered seawater to measure nutrient exchange. The flux of nutrients between the intertidal sediments and settled particles and seawater was estimated from incubation experiments and the observed nitrogen content in surface sediments and suspended particulate material. There was a net import of dissolved nitrate and silicate into Cumberland Basin from Chignecto Bay during early summer, at all other times there was a net export. Despite the low primary productivity and rigorous physical environment, biological activity has a measurable impact on dissolved nutrient concentrations in the waters of Cumberland Basin.  相似文献   

7.
Fecal pellets from the pelagic crab Pleuroncodes planipes were a substantial portion of the particulate organic matter in a sediment trap deployed at the bottom of the mixed layer in the eastern tropical North Pacific Ocean. The lipids of fresh P. planipes feces were compared to lipids of the sediment trap material, of mixed zooplankton which may comprise part of the diet of the crab, and of the crab itself in order to elucidate the source of organic compounds found in the trap. Hydrocarbons, wax esters, triacylglycerols, steroidal alcohols, steroidal ketones, and fatty acids were determined by capillary gas chromatography and gas chromatography/mass spectrometry. Significant input of lipids via sedimentation of crab fecal material is indicated, and modification of dietary lipid within the gut of the crab is inferred. Labile dietary fatty acids are depleted and sterols enriched in the fecal pellets and trap material relative to the zooplankton and crab. Nuclear saturated and unsaturated 3-ketosteroids and unsaturated steroidal hydrocarbons were detected in the crab, its feces, and in the sediment trap particulate material.  相似文献   

8.
The vertical flux and free steroid alcohol (sterol) and ketone composition of particulate material was determined using sediment traps deployed at 389, 988, 3755 and 5068 m at a station in the equatorial North Atlantic, PARFLUX E. Cholest-5-en-3β-ol (cholesterol) was found to be the dominant sterol in all the traps. This compound had a maximum flux at 988 m, accounting for more than 90% of the sterols at this depth. Inputs from mesopelagic Zooplankton populations living in or migrating to depths between the 389 and 988 m traps appear to be responsible for this distribution. The deeper two traps exhibited an increased flux of phytosterols relative to cholesterol, probably due to (a) the incorporation of labile phytoplankton remains in fecal pellets and rapid transport into the deep sea and (b) differential dissolution of heterogeneous large particles. A maximum of 5–22% of the sterols produced in the euphotic zone were present in the 389 m trap. This value drops to less than 1% for the 5068 m trap, 200 m above the sediment surface.In general steroid ketone fluxes gradually decreased with depth. Δ4-Stenones were found in greater abundance than their saturated counterparts. Cholest-4-en-3-one was the major steroid ketone detected in all the traps. A five-fold increase with depth in the cholest-4-en-3-one to cholesterol ratio is most likely due to microbial oxidation of sterols to steroid ketones, or higher Δ4-stenone inputs relative to sterols from organisms.  相似文献   

9.
Polycyclic aromatic hydrocarbon (PAH) and aliphatic hydrocarbon concentrations have been determined for sediments and associated pore waters collected at 2 sites (11 stations) in Puget Sound, Washington (northwest U.S.A.). These sediments have been contaminated to varying degrees by hydrocarbons from a creosote plant and from various combustion sources. PAH were not detected in pore waters of sediments whose PAH were primarily derived from combustion and natural sources, even though pore water concentrations predicted from sediment concentrations and two-phase equilibrium partitioning models were above detection limits from most PAH. Equilibrium partition coefficients calculated from field aqueous and solid phase data from an area contaminated with creosote agreed with laboratory-derived coefficients to within a factor of ± 4. Pore water concentrations of creosote-derived aliphatic hydrocarbons increase with increasing concentration in bulk sediments. However, pore water concentrations of natural and contaminant aliphatic hydrocarbons are much higher than predicted by solubility data, possibly due to association with nonfilterable dissolved organic matter and colloids. Other major factors controlling hydrocarbon pore water concentrations include differential hydrocarbon sources, specific particle associations and solubility.  相似文献   

10.
Sediment trap deployments in estuaries provide a method for estimating the amount of organic material transported to the sediments from the euphotic zone. The amino acid composition of suspended particles, benthic sediment, and sediment-trap material collected at 2.4 m, 5.8 m, and 7.9 m depths in the Potomac Estuary was determined in stratified summer waters, and in well-mixed oxygenated waters (DO) in late fall. The total vertical flow, or flux, of material into the top traps ranged from 3 g m?2 d?1 in August to 4.9 g m?2 d?1 in October. The carbon and nitrogen fluxes increased in the deepest traps relative to the surface traps during both sampling periods, along with that of the total material flux (up to 47.3 g m?2 d?1 in the deepest trap), although the actual weight percent of organic carbon and organic nitrogen decreased with depth. Amino acid concentrations ranged from 129 mg g?1 in surface water particulate material to 22 mg g?1 in particulate material in 9-m-deep waters and in the benthic sediment. Amino acid concentrations from 2.4-mg-depth sediment traps averaged 104±29 mg g?1 in stratified waters and 164±81 mg g?1 in well-mixed waters. The deep trap samples averaed, 77.3±4.8 mg g?1 amino acids in summer waters and 37±16 mg g?1 in oxygenated fall waters. Amino acids comprised 13% to 39% of the organic carbon and 12% to 89% of the orgnaic nitrogen in these samples. Analysis of the flux results suggest that resuspension combined with lateral advection from adjacent slopes can account for up to 27% of the material in the deep traps when the estuary was well-mixed and unstratified. When the estuary was stratified in late summer, the amino acid carbon produced by primary productivity in the euphotic zone decreased by 85% (86% for total organic carbon) at the pycnocline at 6 m depth, leaving up to 15% of the vertical organic flux available for benthic sediment deposition.  相似文献   

11.
This study focused on planktic foraminifera in plankton tows and surface sediments from the western Indian sector of Southern Ocean in order to evaluate the potential foraminiferal secondary calcification and/or dissolution in the sediment. It is found that the symbiotic foraminiferal species are abundant in the subtropical region, whereas non-symbiotic species dominate in the sub-Antarctic and polar frontal regions. The distribution of the symbiotic and non-symbiotic foraminiferal species is controlled by temperature, salinity, light, nutrients and phytoplankton biomass. There is also a lateral southern extent in abundance of planktic foraminifera from surface sediments to plankton tows. The shell weights of the planktic foraminifera N. pachyderma, G. bulloides and G. ruber within the surface sediments are on an average heavier by 27%, 34% and 40% respectively than shells of the same size within the plankton tows, indicative of secondary calcification. The planktic foraminiferal isotopes show the presence of heavier isotopes in the surface sediment foraminifera as compared to plankton tows, thus confirming secondary calcification. Secondary calcification in G. ruber occurs in the euphotic zone, whereas in case of N. pachyderma and G. bulloides it is at deeper depths. We also observed a decrease in the shell spines in surface sediment foraminifera as compared to plankton tows, indicative of the morphological changes that foraminifera underwent during gametogenesis.  相似文献   

12.
 The amounts and types of extractable hydrocarbon components in sediment cores from the Rochester Basin of eastern Lake Ontario provide a record of environmental changes that have accompanied the settlement and population growth of the surrounding land areas. Sediments deposited prior to the mid-1800s contain low concentrations of hydrocarbons that are dominated by land-plant wax components. Concentrations begin to rise in the late 1800s as erosion of soil and nutrients from watershed areas accelerated. This pattern continues into modern times. Episodes of enhanced aquatic productivity are sometimes recorded in twentieth-century sediments by the dominance of algal hydrocarbons, but land-plant components typically predominate. Petroleum residues begin to appear in sediments deposited in the late 1800's but remain minor constituents of the hydrocarbon contents of modern sediments in the Rochester Basin. Received: 21 March 1995 · Accepted: 11 August 1995  相似文献   

13.
Biodeposition rates were studied for a fouling community with a biomass of 6–10 kg per m2 dry wt including shells in which the barnacle Balanus eburneus was a dominant species. The fouling community filtered Indian River lagoon water containing 2–15 mg per 1 mud-size particles and deposited them as sand-size fecal pellets. Measurements of the fecal pellet flux by sediment traps indicated seasonal variations between 16.7 and 74.8 g per m2 per day. A significant correlation was found between fecal pellet flux and temperature (r=0.90; p<0.001). The average flux of fecal pellet deposition was four times greater than the average flux of suspended particle settling without biological influence. Suspended sediment concentration did not significantly affect the rate of biodeposition. Annual biodeposition was 18 kg per m2.  相似文献   

14.
The concentration of solvent-extractable (SE) and bound hydrocarbons, ketones, alcohols, sterols, monocarboxylic acids, hydroxyacids and α,ω-dicarboxylic acids of a surface sample (0–2.5 cm) from a recent carbonate tropical sediment taken at 60ft (18m) depth north-west of the Low Isles, North Queensland, are reported in detail. n-Alkanes are a minor constituent in the SE and bound hydrocarbon fractions with the major component being unresolved complex hydrocarbon material which is not an anthropogenic input. 6,10,14-Trimethylpentadecan-2-one derived from chlorophyll, as well as phytol, were identified as major components of the ketone and alcohol constituents. No chlorophyll pigments or pigmented degradation products were present, implying degradation before incorporation into the sediment. This conclusion is consistent with evidence for higher-plant input in which all sensitive lipids have been degraded before incorporation. SE and bound fractions have been studied in detail and show considerable differences probably arising from the importance of viable biomass in the SE fraction. Inputs to the sediment are determined as higher plants, algae, bacteria, fungi and meiofauna in descending order of importance.  相似文献   

15.
A 24-cm long sediment core from an oxic fjord basin in Ranafjord, Northern Norway, was sliced in 2 cm sections and analysed for As, Co, Cu, Ni, Hg, Pb, Zn, Mn, Fe, ignition loss and Pb-210. Partitioning of metals between silicate, non-silicate and non-detrital phases was assessed by leaching experiments, in an attempt to understand the mechanisms of surface metal enrichment in sediments. Relative to metal concentrations in sediments deposited in the 19th century, metals in near surface sediments were enriched in the following order: Pb > Mn > Hg > Zn > Cu > As > Fe. Cobalt and Ni showed no enrichment. The non-detrital fraction of Cu, Pb, Mn and Zn was significantly higher in the upper 10 cm than at greater depth in the core. This corresponds to sediments deposited since 1900, when mining activities started in the area. The enrichment of Cu, Pb and Zn is assumed to be mainly a result of mining, while Mn is apparently enriched in the surface due to migration of dissolved Mn and precipitation in the oxic surface layer. Elevated concentrations of As and Fe in the upper 4 cm are presumably due to discharges from a coke plant and an iron works respectively. The excess Hg present in the near surface sediments is tightly bound, either in coal particles or ore dust introduced by local industry, or via long distance transport of atmospheric particles. Calculations of metal flux to the sediments indicate an anthropogenic flux of Zn equal to its natural flux, while the flux of Pb shows a threefold increase above natural input.  相似文献   

16.
The adsorption of thirteen trace metals from seawater was studied on interfacial sediment from MANOP site H. The adsorption data indicate a long (~20 day) equilibration time for most metals, an increase in adsorption with an increase in pH and particle concentration, a dependence of adsorption on total metal concentration at high adsorption densities, and a lack of correlation between metal binding ability and metal hydrolysis in solution.Apparent equilibrium binding constants normalized to the total number of available sites on the solid were determined for metal binding with the interfacial sediment. The binding constants indicate that the affinity sequence for metal interactions with the interfacial sediment is: Pb > Fe > Sn ? Co≈ Mn > Cu > Be > Sc ? Zn > Ni > Cd ? Ba > Cs at pH 7.82 in seawater.A comparison of the binding constants for suspended particles, interfacial sediment, and surface sediment indicate that the composition of particles influences the binding ability of the particles. Biogenic particles tend to bind most metals more strongly than lithogenic or authigenic particles.Based on limited data, there is a strong positive correlation between the measured binding constants and the observed partitioning of metals between sediment and seawater.  相似文献   

17.
Seasonal sampling and analysis of surface sediments from the Georges Bank region off the northeastern coast of the United States over a year (1977) have revealed a dynamic hydrocarbon geochemical system. Hydrocarbons of a terrigenous origin appear to be in overall steady state, while marine biogenic hydrocarbons are deposited and then eroded from the surface sediments, eventually being redeposited in a silt depositional region to the west of the Bank. Indirect evidence suggests that anthropogenic hydrocarbons are strongly associated with the silt-clay sediment fraction, while terrigenous plant waxes dominate the coarser fractions. Relationships of an odd-even n-alkane predominence index (OEPI) and total organic carbon (TOC) and that of total hydrocarbons (THC) to TOC are explored as interpretive tools. Finally, the implications of the dynamic transport picture are discussed in terms of pollutant inputs to the region.  相似文献   

18.
The concentrations of lipids were determined in atmospheric particle, gas and rain samples collected from the tropical North Pacific to assess lipid sources, transport mechanisms and fluxes to the ocean surface. Four lipid compound classes (aliphatic hydrocarbons, fatty alcohols, fatty acid esters, and salts) all unequivocally show a terrestrial vascular plant source. These aerosol lipids originate from wind erosion of Asian and American soils and direct emission from vegetation. The major fluxes result from rain rather than dry deposition. These fluxes are large enough to have a major potential impact on the inventory of terrestrially derived lipid material found in deep-sea sediments. This has been showm for n-alkanes, fatty alcohols, fatty acids, total lipids and for organic carbon. By comparing atmospheric and sediment trap fluxes with sediment accumulation rates, it is suggested that some biogenic terrestrial material is more protected from degradation than marine-derived material.  相似文献   

19.
The varved sediments that accumulate in the Cariaco Basin provide a detailed archive of the region’s climatic history, including a record of the quantity of fluvial and wind-transported material. In this study, we examine the sedimentological characteristics (clay mineralogy and grain size) of both surface sediments and sinking lithogenic material collected from sediment trap samples over a three-year period from 1997 to 2000. Data from biweekly sediment trap samples show a tri-modal particle size distribution, with prominent peaks at 2, 22 and 80 μm, indicating sediment contributions from both eolian and fluvial sources. The clay mineralogy of the water column samples collected from 1997 to 1999 also shows distinctive characteristics of eolian and fluvial material. An examination of surface sediment samples from the Cariaco Basin indicates that the Unare River is the main source of riverine sediments to the eastern sub-basin. By combining these sedimentological proxies, we estimate that ～10% of the terrigenous material delivered to the Cariaco Basin is eolian, while ～90% is fluvial. This represents an annual dust accumulation rate of ～0.59 mg/cm2/yr. Since aerosols are closely linked to climate variability, the ability to quantify paleo-dust fluxes using sedimentological characteristics will be a useful tool for future paleoclimate studies looking at sub-Saharan aridity and latitudinal migration of the Intertropical Convergence Zone.  相似文献   

20.
海洋浮游动物粪便通量   总被引：4，自引：1，他引：4  
海洋浮游动物粪便颗粒的沉降被认为是碳从海洋表层向海底输送的主要途径之一，对研究碳通量和水层－底栖耦合具有重要意义。综述了有关浮游动物粪便的形态、产生率、分解速度和沉降速度的研究，以及近年来沉积物捕捉器样品的研究。虽然通过粪便产生率和沉降速度估计出的粪便通量很大，但是沉积物中粪便颗粒造成的碳通量所占比例不大。因此，对其它沉积途径的研究不容忽视。  相似文献   

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