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1.
Shallow surface sediment samples from the Mesopotamian marshlands of Iraq were collected and analyzed to determine the distribution, concentrations and sources of aliphatic lipid compounds (n-alkanes, n-alkanols, n-alkanoic acids, and methyl n-alkanoates) and molecular markers of petroleum in these wetlands. The sediments were collected using a stainless steel sediment corer, dried, extracted with a dichloromethane/methanol mixture and then analyzed by gas chromatography-mass spectrometry (GC–MS). The aliphatic lipid compounds included n-alkanes, n-alkanoic acids, n-alkanols and methyl n-alkanoates with concentrations ranged from 6.8 to 31.1 μg/g, 4.1 to 5.0 μg/g, 5.9 to 7.7 μg/g and from 0.3 to 5.9 μg/g, respectively. The major sources of aliphatic lipids were natural from waxes of higher plants (24–30%) and microbial residues (42–30%), with a significant contribution from anthropogenic sources (27–30%, petroleum), based on the organic geochemical parameters and indices. Further studies are needed to characterize the rate, accumulation and transformation of various organic matter sources before and after re-flooding of these wetlands.  相似文献   

2.
Herein, lipid biomarker analysis is applied to surface sediments from the southeastern Niger Delta region for the quantitative determination of aliphatic lipids, steroids and triterpenoids in order to differentiate between natural (autochthonous vs. allochthonous) and anthropogenic organic matter (OM) inputs to this deltaic environment. This ecosystem, composed of the Cross, Great Kwa and Calabar Rivers, is receiving new attention due to increased human and industrial development activities and the potential effects of these activities impacting its environmental health. While the presence of low molecular weight n-alkanes (<C22) and the fossil biomarkers pristane and phytane in all samples, are indicative of a minor petroleum related input, the total extractable organic component of the surface sediments of these rivers remains predominantly of a natural origin as characterized by the variety and predominance of lipid classes that are mainly derived from the epicuticular waxes of vascular plants and include n-alkanes, n-alkanols, n-alkan-2-ones, n-alkanoic acids, steroids and triterpenoids. In addition, recent OM inputs from microorganisms are indicated by the presence of lower molecular weight n-alkanoic acids (Cmax = 16), while the major triterpenoids of the sediments, taraxerol and friedelin, and the major sterol, sitosterol, indicate recent OM inputs from vascular plants. Plankton-derived sterols, such as fucosterol and dinosterol, are also found in sediments from the Cross and Great Kwa Rivers and likely originate from autochthonous primary productivity. Furthermore, the coprosterols coprostanol and 24-ethylcoprostanol are present in most samples and indicate measurable anthropogenic contributions from domestic untreated sewage inputs and agricultural run-off, respectively. Of the three rivers studied, the Cross River system was excessively influenced by human and industrial development activities, including drivers such as urbanization and population center growth, land-use change to support agricultural production and animal husbandry, and petroleum exploration and production. These influences were found to be regionally specific as controlled by point sources of pollution based on the relative distributions measured and on the fact that the molecular characteristics of sedimentary OM were not distributed smoothly along a gradient.  相似文献   

3.
River runoff and atmospheric fallout (dust and air particulate matter) are major input sources of natural and anthropogenic terrestrial organic and inorganic components to the Arabian seas. In this study, we report on the various lipid tracer compounds that might be transported to the Arabian Gulf by rivers, dust, and air particulate matter. These are based on geochemical analysis of sediment, dust, and particulate samples collected from Iraq, Kuwait, and Saudi Arabia. The samples were extracted with a dichloromethane/methanol mixture and analyzed by gas chromatography-mass spectrometry. The extractable organic compounds (lipids) in the samples include n-alkanes, n-alkanoic acids, n-alkanols, methyl n-alkanoates, steroids, triterpenoids, carbohydrates, and petroleum hydrocarbons. The steroids and triterpenoids were major components in river and wetland samples. The major sources of these lipids were from natural vegetation, microbial (plankton and bacteria) residues in the sediments, sand, and soils, with some contribution from anthropogenic sources. Accordingly, these sources could be major inputs to the Arabian seas besides the autochthonous marine products. Future studies of the organic and inorganic biogeochemistry on river, dust, and coastal areas are needed to characterize the various regional sources, transformation, and diagenetic processes of the organic matter en route to the marine environment.  相似文献   

4.
Soil and sand fine particles, which may be resuspended as fine dust in the atmosphere, contain a variety of anthropogenic and natural organic components. Samples of fine soil and sand particles (sieved to <125 μM) were collected from the Riyadh area in the summer of 2003 and extracted with a mixture of dichloromethane and methanol (3:1, v:v). The derivatized total extracts were analyzed by gas chromatography–mass spectrometry in order to characterize the composition and sources of the organic components. Both anthropogenic and natural biogenic inputs were the major sources of the organic compounds in these extracts. Discarded plastics and vehicular emission products were the major anthropogenic sources in the fine particles from populated areas of the city. Their tracers were plasticizers, UCM, n-alkanes, hopanes and traces of steranes. Vegetation was the major natural source of organic compounds in samples from outside Riyadh and included n-alkanols, n-alkanoic acids, n-alkanes, methyl alkanoates, sterols and triterpenoids. Carbohydrates had high concentrations (42–54%) in all samples and indicate sources from decomposition of cellulose and/or the presence of viable microbiota such as bacteria and fungi. The results were also compared with the data obtained in winter 2002 and showed that anthropogenic inputs were higher in summer than in winter, whereas the opposite trend was observed for natural inputs.  相似文献   

5.
We analyzed speleothem calcite from the Oregon Caves National Monument, southwestern Oregon, to determine the preservation, distribution, concentrations and sources of aliphatic lipid compounds preserved in the calcite. Maximum speleothem growth rate occurs during interglaciations and minimum during glacial intervals. Concentrations of the total lipid compounds range from 0.5 to 12.9 μg g−1. They increase at times of low speleothem growth rate, suggesting dilution, whereas the apparent accumulation rate of lipid compounds tends to be highest during times of fastest speleothem growth rate. Such increased accumulation generally corresponds to times of warm (interglacial) climate, suggesting either a greater source of organic materials during interglacial times and/or greater efficiency of compound capture during more rapid calcite growth. Aliphatic lipid compounds include homologous n-alkanoic acids, n-alkanols and methyl n-alkanoates and sterols with concentrations ranging from 0.3 to 7.8 μg g−1, 0.4 to 1.1 μg g−1, 0.5 to 9.6 μg g−1 and 0.1 to 2.7 μg g−1, respectively. Minor amounts of branched methyl n-alkanoates and dimethyl n-alkanedioates are also present. The high concentrations of methyl n-alkanoates are the result of esterification reactions of free fatty acids in alkaline solutions with high pH values associated with the dripping cave waters. The distribution patterns and geochemical parameters and indices indicate that the major sources of the aliphatic lipids involved leaching from higher plants and microbial residues derived from the soil zone above the cave system. The estimated percentage of microbial inputs ranged from 42 to 90% of the total lipids and also showed an increase in accumulation during warm climates. These well-preserved lipid compounds in speleothem calcite could be used as biomarkers for paleoenvironmental study.  相似文献   

6.
Sediment samples from the coastal zone of the Gulf of Suez contain a variety of organic compounds from anthropogenic and natural sources. A total of 12 surface samples of bottom sediments were collected with an Ekman grab sampler along an off-shore transect south of Ras Abu el-Darag. The samples were extracted with a mixture of dichloromethane and methanol (3:1 v/v) after drying and sieving through 250 μm mesh. The extracts were derivatized and analyzed by gas chromatography–mass spectrometry in order to characterize the chemical composition and sources of the organic components. Marine with minor terrestrial biota were the major natural sources of organic tracers and included n-alkanoic acids, sterols and saccharides (5.7–76.7%). Anthropogenic sources, from petroleum related activities, detergent usage for spill cleaning and littering, are indicated by the presence of n-alkanes with carbon preference index ≤1.0, hopanes, steranes, unresolved complex mixture of branched and cyclic hydrocarbons, alkyl nitriles, alkamides and plasticizers. Their total relative concentrations ranged from 23.3 to 97.3% of the total extracts. Petroleum residues from natural seepage may also be part of these hydrocarbons. The levels of anthropogenic inputs decrease from about 94% in coastal zone sediments to about 20% in sediments from the reef front.  相似文献   

7.
Lipids extracted from lacustrine deposits in the paleolake Qarhan of the Qaidam basin in the northeastern Tibetan Plateau were determined by conventional gas chromatography-mass spectrometry. Several series of biomarkers were identified, mainly including n-alkanes, n-alkan-2-ones, n-alkanoic acids, branched alkanes, triterpenoids and steroids, indicative of various biogenic contributions. On the basis of cluster analysis, the n-C15, n-C17, n-C19 alkanes were proposed to be derived from algae and/or photosynthetic bacteria, the n-C21, n-C23, n-C25 homologues from aquatic plants, and the n-C29, n-C31 homologues from vascular plants. In contrast, the n-C27 alkane is not categorized in the n-C29 and n-C31 group of alkanes, probably due to more complex origins including both aquatic and vascular plants, and/or differential biodegradation. Stratigraphically, layers-2, 4 and 5 were found to show a close relationship in n-alkane distribution, associated with a positive shift in carbon isotope composition of bulk organic matter (δ13Corg), inferring a cold/dry period. Layers-1 and 6 were clustered together in association with a negative δ13Corg, excursion, probably indicating a relatively warm/humid climate. The potential coupling between the n-alkane distributions and δ13Corg, suggests a consequence of vegetation change in response to climate change, with the late MIS3 being shown to be unstable, thought to be the climatic optimum in the Tibetan Plateau. Our results suggest that the cluster analysis used in this study probably provides an effective and authentic method to investigate the n-alkane distribution in paleolake sediments.  相似文献   

8.
The molecular distributions of homologous aliphatic lipid compounds (n-alkanes, n-alkanoic acids, n-alkanols, n-alkanals and n-alkan-2-ones) were investigated in sediments of Lake Bera, Malaysia as well as in plant waxes from the vicinity using gas chromatography-mass spectrometry. In addition, triterpenoids of the oleanane, ursane, lupane and friedelane series, and their diagenetic products were also identified. Using the aquatic proxy Paq, it was found that the n-alkanes present in surface sediments S1, S5 and S6 correspond to an input from emergent macrophytes, whereas in sediments collected from open water (S2, S3 and S4) they correspond to input from submerged/floating macrophytes. The presence of n-alkan-2-ols, a commonly found homologous series in the sediments as well as in the plant wax, is novel here. In addition, the presence of 24-methylcycloart-22-enol and 24-ethylcycloart-22-enol in sediments as well as the plant wax of Pandanus helicopus, a dominant reed around the lake, also supports the input of plant biomarkers to the sediments. The occurrence of 5-membered ring triterpenoid derivatives as major diagenetic products of the triterpenoids identified (e.g. friedelan-2,3-dione) shows that the degradation of the organic matter in the sediments occurs mainly under oxic conditions. Also, the presence of ring-A degraded triterpenoids (dihydroputranjivic acid, 3-nor-2,4-seco-friedelane, 4α- and 4β-3-norfriedelanes, A-norfriedel-10-one, and A-norfriedel-8-en-10-one) and the aromatized triterpenoid hydrocarbons (mono- and triaromatic derivatives) as minor diagenetic products indicates photochemical and microorganism-mediated alteration reactions of natural products in the sediments. Additional novel polyfunctional friedelane derivatives, namely friedelane-2,3-dione, friedelane-1,3-diol-2-one and friedel-1(10)-ene-1,3-diol-2-one were identified for the first time in this study. These novel polyfunctional triterpenoids were inferred to derive from the oxidation of the triterpenoids from higher plants in this oxic tropical environment. For future reference purposes, the mass spectra of the identified polar triterpenoids are also presented here. This study provides important data on the biogeochemistry of organic matter in a tropical lake of SE Asia.  相似文献   

9.
The structural attributes and zonation patterns of mangrove forests in a dry environmental setting were evaluated in relation to gradients of soil resources, soil regulators, and hydroperiod between October 2000 and August 2001 in the Gulf of Fonseca, Honduras. Transects perpendicular to the edge of tidal channels were established at four mangrove sites, each sectioned into three mangrove zones (fringe, transition, and scrub) based upon distinct tree-height gradients. Porewater sulfide concentrations among zones were normally below levels of detection (<0.03 mM) and mean redox values ranged from 163.4±9.9 to −42.4±15.8 mv, indicating slightly reducing conditions in all zones. Mean porewater NOx − and PO4 3− concentrations were not significantly different among zones and ranged from 3.3±0.5 to 4.5±0.4 μM and from 0.05 ±0.02 to 0.18±0.04 μM, respectively. Soil nitrogen concentrations were 1–3 mg g−1 in all zones, and mean nitrogen:phosphorus atomic ratios were <20 (range: 12.9–14.9), indicative of fertile wetland soils. Mean basal areas were significantly different among mangrove zones (fringe > transition) and were coupled with differences in height within species and zones.Avicennia germinans occupied areas with higher elevations associated with higher salinities ranging from 80 to 140 g kg−1 in the dry season.Rhizophora mangle dominated lower elevations where salinities ranged from 38 to 57 g kg−1 in both the dry and wet seasons. Spatial analysis on mangrove seedlings along transects confirmed that seedling distribution along the intertidal profile was statistically correlated with conspecific adults, indicating that survival and growth of seedlings in different intertidal locations are closely matched to canopy membership. The sharp transition (<100 m) in forest structure and distribution of mangrove species along the intertidal zone of subhumid coastal environments demonstrate common zonation patterns where species distribution and species-specific habitat suitability are mediated closely with tolerance to soil regulators (high soil salinity) rather than resource availability.  相似文献   

10.
Lake Kivu is a gas-charged East African rift lake with currently anoxic bottom water. The extractable compounds and residual organic matter of a short sediment core have δ13C values typical of lacustrine microbial detritus. The total extracts consist primarily of polar compounds such as n-alkanoic acids, hydroxyalkanoic acids, triterpenoids, steroids and monosaccharides, with minor amounts of n-alkanes and n-alkanols. These tracer compounds and δ13C values indicate that the organic matter in the surficial and deeper sedimentary record was dominated by bacterial sources. The sapropelic sediment between these horizons contains organic matter from primarily algal with lesser bacterial input. Terrestrial organic markers are minor in all samples. The major fractions of the compounds in the total extracts were oxidized in the upper water column prior to transit through the anoxic bottom water to sedimentary deposition. The sapropelic horizon may reflect lake water turnover with ventilation or hydrothermal activity and consequently increased algal blooms.  相似文献   

11.
With the aim of evaluating temporal changes in sedimentation and organic carbon (Corg) supplied over the last ~100 years, a sediment core was collected at Soledad Lagoon, a costal ecosystem surrounded by mangroves, located in the Cispatá Estuary (Caribbean coast of Colombia). The core sediments were characterized by low concentrations of calcium carbonate (0.2–2.9%), organic matter (3–8%), total nitrogen (0.11–0.38%), and total phosphorus (0.19–0.65 mg g−1). Fe and Al concentrations ranged from 4% to 5%, and Mn from 356 to 1,047 μg g−1. The 210Pb-derived sediment and mass accumulation rates were 1.54 ± 0.18 mm year−1 and 0.08 ± 0.01 g cm−2 year−1, respectively. The sediment core did not provide evidence of human impact, such as enhancement of primary production or nutrient enrichment, which may result from recent land uses changes or climate change. The Corg fluxes estimated for Soledad Lagoon core lay in the higher side of carbon fluxes to coastal ecosystems (314–409 g m−2 year−1) and the relatively high Corg preservation observed (~45%) indicate that these lagoon sediments has been a net and efficient sink of Corg during the last century, which corroborate the importance of mangrove areas as important sites for carbon burial and therefore, long-term sequestration of Corg.  相似文献   

12.
Multi-biomarkers were characterized in surface soils with different vegetation during an annual cycle in Oregon, U.S.A., to study the composition and dynamics of soil organic matter (SOM). The major compound classes identified include saccharides, steroids, terpenoids, and homologous series of aliphatic lipids (n-alkanoic acids, n-alkanols, and n-alkanes). Saccharides, n-alkanoic acids, and sterols were the most dominant compound groups identified in Ryegrass field soils, whereas n-alkanoic acids, n-alkanols, and sterols were dominant in soils under conifer and deciduous vegetation. Plant species, instead of microbial organisms, was found to be the primary source influencing the concentration and distribution of the major biomarker tracers in the studied surface soils. Over an annual cycle, concentrations of higher plant lipids such as monoacyl glycerides, sterols, n-alkanoic acids and total wax were higher during summer (especially June–August). During fall into winter, the concentrations of all compounds decreased to steady state levels due to cessation of de novo synthesis and concomitant biodegradation and remineralization of detritus. Sucrose and glucose reached maximum concentrations during spring (especially March–May), which could be related with plant growth, especially rootlets in the soils. Mycose, the microbial/fungal metabolite, maximized during late summer, suggesting the concomitant increase of microbial/fungal activity with the increasing primary production. The composition and variation of biomarkers observed over an annual cycle improved our understanding of SOM dynamics in temperate soils, which could also be linked to regional and global carbon cycles.  相似文献   

13.
This study provides a reconstruction of the environmental evolution since 128 ka recorded by the lipid biomarkers of the C15–C35 n-alkanes, the C13–C33 n-alkan-2-ones and the C12–C30 n-alkanols isolated from the Tawan loess section, Northwest China. Variations in paleoenvironment are reconstructed from the values of the carbon preference index (CPI), the average chain length (ACL), the L/H (ratio of lower-molecular-weight to higher-molecular-weight homologues), the n-alkane C27/C31 ratios, and the n-alkan-2-one C27/C31 ratio. These parameters indicate the dominance of grasses over the west Chinese Loess Plateau (CLP) during the late Pleistocene. Lower values of the CPI and the ACL values, respectively, indicate stronger microbial reworking of organic matter and changes in plant species, which are both indicative of a warmer-wetter environment. Furthermore, the fluctuations of environment recorded in the Tawan section exhibit ten phases that show obvious cycles between warm periods and cold intervals. This study reveals that changes in the biomarker proxies agree well with changes in the magnetic susceptibility and grain size, and it indicates a huge potential for paleoenvironmental reconstructions by using the n-alkan-2-one and n-alkanol proxies.  相似文献   

14.
Stable carbon (δ13C) and hydrogen (δD) isotopic compositions of n-alkanes, anteiso-alkanes, n-alkanoic acids, n-alkanols, phytol and sterols in raw leaves of Acer argutum and Acer carpinifolium, their fallen leaves, mold and soils from a natural Acer forest were measured in order to: (1) understand isotopic variation of the plant biomarkers in a plant-soil system and (2) evaluate which biomarker is the most effective recorder of soil vegetation. Long-chain (> C24) n-alkanes, n-alkanoic acids and n-alkanols are gradually enriched in 13C up to 12.9‰ (average of 4.3‰) and depleted in D up to 94‰ (average of 55‰) from raw leaves to soils. However, anteiso-alkanes, phytol and sterols show little variation in both δ13C (< ± 1‰) and δD (< ± 2‰) from raw leaves to soils. These isotope signatures in a plant-soil system indicate that isoprenoid plant biomarkers such as sterols in soils faithfully preserve the isotopic compositions of dominant higher plants growing on the soils without a diagenetic effect upon the isotopic compositions. In contrast, long-chain n-alkyl molecules in soils undergo specific isotopic modification during biodegradation associated with early diagenesis and/or a significant contribution from heterotrophic reworking.  相似文献   

15.
Phosphatase activity was measured in sediments from tidal freshwater habitats adjacent to the Cooper River in South Carolina representing different stages of ecological succession. It was found that sediment (0–5 cm) acid phosphatase activity, alkaline phosphatase activity and phosphodiesterase activity increased with increasing successional stage and phytomass. Acid phosphatase activity in creased from 7.5±1.2 (±1 SD) in subtidal sediment from a shallow open water habitat without vegetation to 61.2±4.9 μmol g−1 hr−1 (μmol of p-nitrophenol released per gram of dry sediment per hour) in intertidal sediments colonized by emergent macrophytes, while alkaline phosphatase activity increased from 2.1±0.1 to 19.01±1.5 μmol g−1 hr−1. Phosphodiesterase activity increased from 1.8±0.1 to 20.2±2.0 μmol g−1 hr−1 along the same gradient. Acid phosphatase activity was highly correlated (R2=0.92, P<0.001) with the organic matter content of the sediment. A study of phosphatase kinetics showed that Vmax of all phosphatases also increased along the successional gradient. Trends in phosphatase activity and Vmax correlated positively with plant biomass and negatively with concentrations of soluble reactive phosphorus in porewater, sediment extractable phosphorus, and total phosphourus. The porewater N∶P atom ratio decreased along the succession gradient from 25.3 in an early stage, open water community to 13.0 in a community dominated by emergent vegetation. The data also show that the distribution of the forms of phosphorus changed with successional stage. The change in distribution and the increased biological demand for phosphorus that paralleled succession were mediated by the activity of phosphatase enzymes.  相似文献   

16.
We present a systematic study of chain-length distributions and D/H ratios of n-alkyl lipids (both n-alkanes and n-alkanoic acids) in a wide range of terrestrial and aquatic plants around and in Blood Pond, Massachusetts, USA. The primary goal is to establish a model to quantitatively assess the aquatic plant inputs of the mid-chain length n-alkyl lipids to lake sediments and to determine the average hydrogen isotopic ratios of these lipids in different plants. Our results show that middle-chain n-alkyl lipids (C21-C23n-alkanes and C20-C24n-alkanoic acids) are exceptionally abundant in floating and submerged aquatic plants, in contrast to the dominance of long-chain n-alkyl lipids (C27-C31n-alkanes and C26-C32n-alkanoic acids) in other plant types, which are consistent with previously published data from Mountain Kenya and the Tibetan Plateau. Combining available data in different environmental settings allows us to establish statistically robust model distributions of n-alkyl lipids in floating/submerged macrophytes relative to other plant types. Based on the model distributions, we established a multi-source mixing model using a linear algebra approach, in order to quantify the aquatic inputs of mid-chain n-alkyl lipids in lake sediments. The results show that ∼97% of the mid-chain n-alkyl lipids (C23n-alkane and C22n-acid (behenic acid)) in Blood Pond sediments are derived from floating and submerged macrophytes. In addition, D/H ratios of C22n-acid and C23n-alkane in the floating and submerged plants from Blood Pond display relatively narrow ranges of variation (−161 ± 16‰ and −183 ± 18‰, respectively). Our study demonstrates that mid-chain n-alkyl lipids such as C23n-alkane and C22n-acid could be excellent recorders of past lake water isotopic ratios in lakes with abundant floating and submerged macrophyte inputs.  相似文献   

17.
Peats in a sediment core from Ruoergai bog, which has a cold and moist plateau climate with major source input from herbaceous plants, have been studied by GC–MS in order to understand the composition and diagenetic processes of lipids in this depositional environment. Long chain components (C21–C35) predominate in the n-alkanes, n-alk-1-enes, n-fatty acids, n-alkan-2-ones and n-alkanols with a maximum of C31, C27, C22 or C24, C23 or C25 and C22, respectively. A herbaceous origin for these long chain compounds is suggested, and this is supported by their stable carbon isotopic compositions. Diterpenoid hydrocarbons with abietane, pimarane and kaurane skeletons, some of which have not been reported often in modern sediments, are prominent and are derived from higher plants. Several triterpenoid ketones and alcohols with oleanane or lupane skeletons, and a series of des-A-triterpenoid hydrocarbons which have not been reported often in modern sediments are also present, and are assigned to a higher plant source. Hopanoids, including their alkanes, alkenes, ketones, alcohols and esters, are abundant and of bacterial origin. Steroid ketones and alkanols are dominated by C29 homologues. C28 and C29 steroids are derived mainly from higher plants, whereas the C27 component is assigned to a microbial source. The presence of short-chain n-alkanes with no odd-even carbon predominance, bacterially derived fatty acids (C14, C15, iso- and unsaturated acids), n-alkan-2-ones, des-A-triterpenoid hydrocarbons, hopanoids and some steroid ketones indicate that intense microbial reworking of the organic matter has taken place in this depositional environment. The chemical and biochemical conversions of some cyclic alkenes to alkanes, such as tricyclic diterpenoids, tetracyclic terpenoids and steroid ketones, are also evident with depth. The dominance of C20 components in the diterpenoid hydrocarbons may reflect an oxidizing or reducing depositional condition.  相似文献   

18.
To determine the degree of hydrocarbon contamination and the contribution of local petroleum industries to contaminant loadings in sediments from the Beiluohe River, China, 12 surface sediment samples were collected for geochemical analysis in 2005. Sediment samples were extracted by organic solvents, separated by silica gel column chromatography and the profiles of n-alkanes, biomarkers and polycyclic aromatic hydrocarbons (PAHs) in sediments were analyzed by gas chromatography with flame ionization detector and gas chromatography/mass spectroscopy. Concentrations of total hydrocarbons in the sediments varied from 12.1 to 3,761.5 μg g−1 dry wt, indicating that most sediments in Beiluohe River was only slightly to moderately contaminated by hydrocarbons. Concentrations of PAHs for six samples (sum of 16 isomers) varied from 17.7 to 407.7 ng g−1 dry wt and at present low levels of PAHs did not cause adverse biological effects in Beiluohe River sedimentary environment. PAH compositions, n-alkanes and biomarker profiles all suggested that there were different sources of contaminations in studied areas. n-Alkanes reflect two distinct sources: a fossil n-alkane series from crude oil at sites S40, S43, S87 and plantwax n-alkanes at sites S39 and S45. Judged by their PAH ratios, the sediments at site S15 were pyrolytic, sediments at S17 and S43 were petrogenic, and sediments at S39, S40 and S64 had a mixture source of pyrolytic and petrogenic.  相似文献   

19.
《Applied Geochemistry》2001,16(1):95-108
Bottom sediments and suspended matter from the shelf and slope areas off northeastern Taiwan were analyzed for sterol, n-alkanol and n-alkane compositions. The Σ(algal sterols/cholesterol) ratios (mean±1σ) were 1.00±0.31 (n=7) for the shelf sediments, 3.29±0.61 (n=7) for the slope sediments, and 1.54±0.19 (n=3) for the suspended matter. The much higher proportion of cholesterol in the shelf sediments is most likely derived from mollusks in the relict sediments. An additional sterol source for the shelf sediments probably is suspended matter in the water column although the shelf has no apparent sedimentation. Results from phytol and n-alkanols suggest recent inputs of lipids from the water column to the shelf. The stanol/stenol ratios are lower for the older shelf sediments than for the younger slope sediments.  相似文献   

20.
Lipid biomarkers from a peat plateau profile from the Northeast European Russian Arctic were analyzed. The peat originated as a wet fen ca. 9 ka BP and developed into a peat bog after the onset of permafrost ca. 2.5 ka BP. The distributions and abundances of n-alkanols, n-alkanoic acids, n-alkanes, n-alkan-2-ones and sterols were determined to study the effect of degradation on their paleoclimate proxy information. Plant macrofossil analysis was also used in combination with the lipid distributions. The n-alkanol and n-alkanoic acid distributions in the upper part of the sequence generally correspond to compositions expected from plant macrofossil assemblages. Their carbon preference index (CPI) values increase with depth and age, whereas those of the n-alkanes decrease. The different CPI patterns suggest that n-alkanoic acids and n-alkanols deeper in the sequence may be produced during humification through alteration of other lipids. Excursions in the n-alkanoic acid content also suggest an important contribution of invasive roots to the lipid biomarker composition. The CPIs associated with these compounds show that under permafrost conditions organic material from Sphagnum is better preserved than material from vascular plants. Increasing stanol/stenol ratio values and decreasing n-alkane CPI values indicate progressive degradation of organic matter (OM) with depth. The n-alkan-2-one/n-alkane and n-alkan-2-one/n-alkanoic acid ratios were shown to be useful proxies that can reflect the degree of OM preservation and suggest that both microbial oxidation of n-alkanes and decarboxylation of n-alkanoic acids produce n-alkan-2-ones in this peat sequence.  相似文献   

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