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1.
Tracing the inputs of bacterial organic carbon to marine systems has been constrained by the lack of distinguishing geochemical tracers and limited contribution in sediments compared to other sources of organic matter. Bacteriohopanepolyols (BHPs) provide a direct means to identify bacterial inputs which also reflect potential bacterial groups and their activities in aquatic systems. We applied recent analytical approaches to identify and quantify bacterial derived carbon contributions to surface sediments from the western Arctic Ocean using BHPs. The abundance and distribution of BHPs resemble trends of water column primary production and suggest active heterotrophic recycling of in situ production with some component of long term preservation. BHPs proposed as terrestrial derived signatures (i.e. adenosylhopanes) were also abundant in western Arctic sediments and reflect offshore trends of other terrigenous lipid signatures with a fraction representing their degradative products. Analysis of BHPs in organic rich peat and surface sediments from two Arctic rivers showed the highest inputs of adenosylhopanes, implying active bacterial recycling of recalcitrant terrigenous material. BHPs observed in western Arctic surface sediments reveal significant contributions of bacteria associated with organic carbon from multiple sources.  相似文献   

2.
A 20 kyr long sediment sequence from the Congo deep sea fan (core GeoB 6518-1), one of the world’s largest deep sea river fans, has been analysed for bulk and molecular proxies in order to reconstruct the marine, soil and plant organic carbon (OC) contributions to these sediments since the last glacial maximum. The bulk proxies applied, C/N ratio and δ13Corg, ranged from 10 to 12.5 and from −24.5 to −21‰ VPDB, respectively. As molecular proxies, concentrations of marine derived alkenones and terrestrial derived odd-numbered n-alkanes were used, which varied between 0.2 and 4 μg/g dry weight sediment. In addition, the branched vs. isoprenoid tetraether (BIT) index, a proxy for soil organic matter input, was used, which varied from 0.3 to 0.5 in this core.Application of binary mixing models, based on the different individual proxies, showed estimates for terrestrial OC input varying by up to 50% due to the heterogeneous nature of the OC. Application of a three end-member mixing model using the δ13Corg content, the C/N ratio and the BIT index, enabled the distinction of soil and plant organic matter as separate contributors to the sedimentary OC pool. The results show that marine OC accounts for 20% to 40% of the total OC present in the deep sea fan sediments over the last 20 kyr and that soil OC accounts for about half (∼45% on average) of the OC present. This suggests that soil OC represents the majority of the terrestrial OC delivered to the fan sediments.Accumulation rates of the plant and soil OC fractions over the last 20 kyr varied by a factor of up to 5, and are strongly related to sediment accumulation rates. They showed an increase starting at ca. 17 kyr BP, a decline during the Younger Dryas, peak values during the early Holocene and lower values in the late Holocene. This pattern matches with reconstructions of past central African humidity and Congo River discharge from the same core and revealed that central African precipitation patterns exert a dominant control on terrestrial OC deposition in the Congo deep sea fan. Marine OC accumulation rates are only weakly related to sediment accumulation rates and vary only little over time compared to the terrigenous fractions. These variations are likely a result of enhanced preservation during times of higher sedimentation rates and of relative small fluctuations in primary production due to wind-driven upwelling.  相似文献   

3.
通过对中国第3次和第4次北极考察在白令海和西北冰洋采集的65个表层样沉积物中生物标记物四醚膜类脂物(GDGTs)的研究,发现西北冰洋表层沉积物中类异戊二烯和支链GDGTs的浓度分布大致以楚科奇海和波弗特海的陆坡为界线,呈现南高北低的特征,这一特征主要与水体生产力和陆源有机质的输入量有关.基于GDGTs的陆源输入指数BIT显示,从楚科奇海北部到高纬度区的阿尔法脊,陆源有机质的相对比例明显增加,与有机碳稳定同位素等结果一致,表明BIT可以用来指示北极陆源有机质输入量的变化.应用前人TEXL86-SST方程估算的研究区表面海水温度SST与现代年均SST和夏季平均SST的相关性较差,原因可能与陆源输入的类异戊二烯GDGTs干扰以及低的古菌生产力有关.从季节性海冰覆盖区到永久性海冰覆盖区,基于支链GDGTs的环化指数CBT明显升高,可能反映了CBT对海冰覆盖状况的响应,但其响应机制还不清楚.基于支链GDGTs的环化指数CBT和甲基化指数MBT估算的北极陆地年均大气温度和土壤pH差异较大,可能是由表层沉积物的来源复杂以及混合作用造成的.  相似文献   

4.
《Quaternary Science Reviews》2004,23(3-4):261-281
The organic carbon content of marine sediments is commonly used as a proxy for export production. However, in continental margin sediments a large fraction of the organic matter may be of terrestrial origin, and it is necessary to correct the total organic carbon data accordingly. Radiocarbon dating of bulk organic carbon, organic geochemistry and isotope data (δ13C and δ15N) are used here to characterize the type of organic matter present in Core JT96-09 collected at a water depth of 920 m on the slope off Western Canada. The quantities of marine and terrestrial organic carbon are then estimated using the δ13C data. The 16 kyr record obtained from Core JT96-09 suggests that accumulation of total organic carbon was highest during the late glacial and deglacial, but geochemical data indicate that as much as 70% of this carbon is terrestrial in origin. When the palaeo-record is corrected for this terrigenous input it is observed that accumulation of marine organic matter, and presumably marine export production, increased at the end of the last glacial contemporaneous with the Bølling, and that it peaked during the Allerød. Data from other palaeoproductivity proxies (i.e., bio-barium, opal and alkenones) also indicate relatively high productivity during the deglacial. These results indicate a return to modern upwelling conditions and high marine export production at ∼14.3 calendar kyr BP and a period of enhanced upwelling, relative to the present, during the Allerød.  相似文献   

5.
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   

6.
Representative samples of crude oils from Cusiana, Cupiagua, Apiay, Castilla and Chichimene fields in the Eastern Llanos Basin of Colombia were analyzed to determine its compound-specific stable carbon isotope composition (CSIA) using gas chromatography–isotopic ratio–mass spectrometry (GC–IRMS). GC–IRMS analyses of n-alkanes allowed differentiating between Cretaceous and Cretaceous/Tertiary oil samples. Cretaceous sourced samples have δ13C-enriched values than Cretaceous/Tertiary sourced samples; the heavier isotope composition of these samples is due to their major terrigenous organic matter input. Their isotope distribution patterns suggest significant algal and/or bacterial contribution (marine origin). The analysis of the n-alkane fractions by GC–IRMS confirms that the organic matter has marine origin in those samples from Cusiana, Cupiagua and Apiay while Castilla and Chichimene have marine origin with terrestrial inputs. The results were confirmed by gas chromatography/FID and gas chromatography/mass spectrometry (GC/MS). Basic geochemical composition show that samples from Cupiagua/Cusiana fields and Apiay/Castilla/Chichimene fields in the Llanos basin, Colombia present different characteristics reflecting a specific for each depositional environment.  相似文献   

7.
With this study, I suggest that changes in biogeochemical processes in northern Norwegian fjords during the last glacial/interglacial transition (14.3 to 6.3 ka B.P.) are predominantly climate induced. Variable strength in Atlantic water inflow, intrusion of Arctic waters and sea-ice coverage, various nutrient supply, as well as several re-advances of continental ice-sheets are recorded by both bulk organic and selected biomarkers in sediments of the Andfjord. Stable isotope (δ13Corg, δ15N) and Rock-Eval pyrolysis data indicate a strong supply of terrestrial organic matter during stadials (e.g., Younger Dryas, Older Dryas) whereas enhanced input of marine organic matter prevailed during the interstadials (Bølling/Allerød). Profiles of selected biomarkers of marine origin show a characteristic climate-induced variation during the whole time interval, where relatively low concentrations of dinosterols and C37 alkenones may indicate—similar to today—a minor contribution of their respective plankton groups (coccolithophorids, dinoflagellates). The prevalence of Arctic waters and seasonal sea-ice coverage during the Younger Dryas is indicated by a single maximum of 24-methylenecholesterol probably indicating the dominance of sea-ice diatoms and/or the prevalence of diatoms of Thalassiosiraceae in surface waters. The sediments of the Allerød, in contrast, show a pronounced maximum in dinosterols, indicating a better adaptation of dinoflagellates to an oceanic regime that is characterized by incipient intrusion of Atlantic water, highly variable sea surface temperatures, and well stratified water masses. The concentration of higher-molecular-weight n-alkanes, however, follows the deglacial-early Holocene trend of climate amelioration from the last deglaciation to the middle Holocene, with maxima during ice advances (stadials) and minima during the middle Holocene warm period.These new results significantly improve the understanding of climate-induced response on organic matter supply in fjords and provide a better knowledge of past variations of biogeochemical processes in high-latitude coastal environments.  相似文献   

8.
Molar organic carbon to total nitrogen to organic phosphorus (OC:TN:OP) ratios are used in tandem with carbon isotopic values to constrain sources of organic matter (OM) to marine sediments in a tropical coastal embayment. Analysis of end-members specific to the study site indicates that the bulk OM pool cannot be modeled as a simple mixture of two end-members (terrestrial vs. marine OM), but rather reflects a more complex, multicomponent mixture. Mangrove, coral reef ecosystems, and bacterial biomass contribute OM to tropical coastal marine sediments that is compositionally distinct from traditional marine and terrestrial end-members and thus preclude the application of a classical two end-member mixing model of the sort that has been used traditionally in sediments from temperate environments. A survey of elemental ratios and carbon isotopic values of potential OM end-members reported in the literature, as well as depth profiles before and after whole-core incubation experiments conducted as part of this study, were used to evaluate the strength of OC:TN versus OC:OP ratios as OM source indices. Our study suggests that OC:TN ratios are a weaker indicator of OM source than OC:OP ratios, because: (1) the more restricted dynamic range of OC:TN ratios prevents clear distinction of terrestrial-from marine-derived OM, and (2) post-depositional changes in OC:TN ratios occur during diagenesis, obscuring the source signature of initially deposited OM. The fidelity of OM indices during early diagenesis underscores the importance of quantifying OP in sediments to assess sedimentary OM source.  相似文献   

9.
Burial of organic carbon (OC) in ocean sediments acts as the ultimate long-term sink for both terrestrial and marine carbon, however, the mechanisms controlling the preservation of this carbon are poorly understood. To better understand these mechanisms, we applied solid-state 13C nuclear magnetic resonance (NMR) spectroscopy, along with elemental, stable carbon isotopic (δ13C) and lignin phenol analyses, to size and density fractions of sediments influenced by either mixed terrestrial and marine OC inputs (Washington Coast slope) or dominantly marine inputs (Mexican Margin). Elemental, isotopic and lignin analyses all reveal that within the Washington Coast sediment, the OC mixes linearly between nitrogen-poor and 13C-depleted, lignin-rich OC in the large and light fractions and nitrogen-rich and 13C-enriched, lignin-poor OC in the small and dense fractions, suggesting that this sediment contains a two-component mixture of terrestrial vascular plant- and marine-derived OC. The integral areas of each of seven NMR spectral regions in the different samples trend linearly when plotted versus δ13C signature, with most R2 values of 0.78 or greater, demonstrating that the NMR spectra of the two sources of carbon also mix linearly between the two endmembers. The terrestrial endmember in this sediment appears to be dominated by lignin and black carbon whereas the source of the marine endmember is less clear from the NMR spectra. In contrast, all of the analyses indicate that OC in the Mexican Margin sediment fractions is homogenous and derives almost exclusively from marine sources. It appears that selective preservation of (bio)chemically recalcitrant lignin and black carbon is the primary mechanism of preservation of terrestrial OC, whereas mineral-protection is the dominant mechanism preserving marine OC in the Washington coast sediment. There is little evidence showing that either preservation mechanism functions in the Mexican Margin sediments.  相似文献   

10.
Glycerol dialkyl glycerol tetraethers (GDGTs) and bulk organic geochemical parameters were examined for a short core from the Bohai Sea, a Yellow River-dominated continental margin. A three end member mixing model using branched/isoprenoid tetraethers (BIT) index, δ13C and C/N shows that the average fractions of soil, marine and plant organic matter (OM) during the period of 1933–2011 are 67.7% (38–92%), 26.1% (0–58%) and 6.2% (0–23%), respectively. Abrupt changes of sedimentary OM compositions around 1953, 1976 and 1996 are synchronous with the Yellow River mouth relocations. The BIT index values (0.33–0.80) present a stronger correlation with crenarchaeol abundance (R2 = 0.88) than branched GDGTs abundance (R2 = 0.27), suggesting that variations of marine Thaumarchaeota abundance rather than soil OM inputs is the first order factor controlling the BIT index values, although this proxy has been widely used for soil OM. The comparison between the BIT index, nutrient status and historical Yellow River sediment load indicates that the high sensitivity of the BIT index to the Yellow River channel shifts cannot be explained by a nutrient stimulation mechanism, but instead is likely caused by the restriction of Thaumarchaeota growth in highly turbid water due to the enormous sediment inputs from Yellow River. Our study demonstrates that local conditions should be considered when applying the BIT index as an environmental proxy.  相似文献   

11.
Analysis of 3-m sediment cores revealed that profiles of carbon (C), sulfur (S), and iron (Fe) varied with relative distance from marine and terrestrial sediment sources in Tomales Bay California. Despite relatively high sedimentation rates throughout the bay (historically 3–30 mm yr−1), sulfate reduction of deposited organic matter led to free-sulfide accumulation in sediments only at the location farthest from terrestrial runoff, the source of reactive iron. Acid-volatile sulfide concentrations in all sediments (<10 μmol g−1) were low relative to concentrations of chromiumreducible sulfide (up to 400 μmol g−1 farthest from the reactive iron source). A calculated index of iron availability, used to describe sediment resistance to build-up of free sulfide, was lowest at this location. Recent, upward shifts in reactive Fe concentration and in the relative contribution of terrestrial orgnic carbon (measured as a shift in δ13C of bulk sediment organic matter) in all cores indicated that erosion and transport of sediments from the watershed surrounding Tomales Bay increased after European settlement in the 1850s.  相似文献   

12.
We measured molecular distributions and compound-specific hydrogen (δD) and stable carbon isotopic ratios (δ13C) of mid- and long-chain n-alkanes in forest soils, wetland peats and lake sediments within the Dorokawa watershed, Hokkaido, Japan, to better understand sources and processes associate with delivery of terrestrial organic matter into the lake sediments. δ13C values of odd carbon numbered C23-C33n-alkanes ranged from −37.2‰ to −31.5‰, while δD values of these alkanes showed a large degree of variability that ranged from −244‰ to −180‰. Molecular distributions in combination with stable carbon isotopic compositions indicate a large contribution of C3 trees as the main source of n-alkanes in forested soils whereas n-alkanes in wetland soil are exclusively derived from marsh grass and/or moss. We found that the n-alkane δD values are much higher in forest soils than wetland peat. The higher δD values in forest samples could be explained by the enrichment of deuterium in leaf and soil waters due to increased evapotranspiration in the forest or differences in physiology of source plants between wetland and forest. A δ13C vs. δD diagram of n-alkanes among forest, wetland and lake samples showed that C25-C31n-alkanes deposited in lake sediments are mainly derived from tree leaves due to the preferential transport of the forest soil organic matter over the wetland or an increased contribution of atmospheric input of tree leaf wax in the offshore sites. This study demonstrates that compound-specific δD analysis provides a useful approach for better understanding source and transport of terrestrial biomarkers in a C3 plant-dominated catchment.  相似文献   

13.
The provenance of organic matter in surface sediments from the northern Gulf of Mexico was investigated by analyzing the compositions of lipid biomarkers (n-alkanes, fatty acids, sterols) liberated after a series of chemical treatments designed to remove different organo-mineral matrix associations (i.e. freely extractable, base-hydrolyzable, unhydrolyzable). Bulk analyses of the organic matter (carbon content, carbon:nitrogen ratios, stable and radiocarbon isotopic analyses) were also performed on the intact sediments and their non-hydrolyzable, demineralized residue. We found recognizable lipids from distinct sources, including terrestrial vascular plants, bacteria and marine algae and zooplankton, within each of the isolated fractions. Based on the lipid signatures and bulk compositions, the organic matter within the unhydrolyzable fractions appeared to be the most diagenetically altered, was the oldest in age, and had the highest abundance of terrigenous lipids. In contrast, the base-hydrolyzable fraction was the most diagentically unaltered, had the youngest ages and was most enriched in N and marine lipids. Our results indicate that fresh, autochthonous organic matter is the most important contributor to base-hydrolyzable lipids, whereas highly altered allochthonous sources appear to be predominant source of unhydrolyzable lipids in the surface sediments from the Atchafalaya River shelf. Overall, the lipid biomarker signatures of intact sediments were biased towards the autochthonous source because many of the organic compounds indicative of degraded, terrigenous sources were protected from extraction and saponification by organo-mineral matrices. It is only after these protective matrices were removed by treatment with HCl and HF that these compounds became evident.  相似文献   

14.
Lignin oxidation products and 13C/12C ratios were compared as indicators of land-derived organic matter in surface sediments from the western Gulf of Mexico. Whole sediments were reacted with cupric oxide to yield phenolic oxidation products that indicated the types and relative amounts of the lignins that were present.Measurements of lignin concentration and carbon isotope abundances both indicated a sharp offshore decrease of land-derived organic matter in most areas of the western Gulf. This decrease results primarily from mixing of terrestrial and marine organic matter. The terrestrially derived material in these sediments has a lignin content similar to that of grasses and tree leaves. Flowering plants contribute most of the sedimented lignin compounds. These lignins apparently occur in the form of well-mixed plant fragments that are transported to sea by rivers and deposited primarily on the inner continental shelf.  相似文献   

15.
We investigated the latitudinal changes in atmospheric transport of organic matter to the western Pacific and Southern Ocean (27.58°N-64.70°S). Molecular distributions of lipid compound classes (homologous series of C15 to C35n-alkanes, C8 to C34n-alkanoic acids, C12 to C30n-alkanols) and compound-specific stable isotopes (δ13C of C29 and C31n-alkanes) were measured in marine aerosol filter samples collected during a cruise by the R/V Hakuho Maru. The geographical source areas for each sample were estimated from air-mass back-trajectory computations. Concentrations of TC and lipid compound classes were several orders of magnitude lower than observations from urban sites in Asia. A stronger signature of terrestrial higher plant inputs was apparent in three samples collected under conditions of strong terrestrial winds. Unresolved complex mixtures (UCM) showed increasing values in the North Pacific, highlighting the influence of the plume of polluted air exported from East Asia. n-Alkane average chain length (ACL) distribution had two clusters, with samples showing a relation to latitude between 28°N and 47°S (highest ACL values in the tropics), whilst a subset of southern samples had anomalously high ACL values. Compound-specific carbon isotopic analysis of the C29 (−25.6‰ to −34.5‰) and C31n-alkanes (−28.3‰ to −37‰) revealed heavier δ13C values in the northern latitudes with a transition to lighter values in the Southern Ocean. By comparing the isotopic measurements with back-trajectory analysis it was generally possible to discriminate between different source areas. The terrestrial vegetation source for a subset of the southernmost Southern Ocean is enigmatic; the back-trajectories indicate eastern Antarctica as the only intercepted terrestrial source area. These samples may represent a southern hemisphere background of well mixed and very long range transported higher plant organic material.  相似文献   

16.
The Maikop Formation, deposited in eastern Azerbaijan during Oligocene and Early Miocene times, contains prolific source rocks with primarily Type II organic matter. Paleontological analyses of dinoflagellate cysts revealed a Lower to Upper Oligocene age for the investigated succession near Angeharan. A major contribution of aquatic organisms (diatoms, green algae, dinoflagellates, chrysophyte algae) and minor inputs from macrophytes and land plants to organic matter accumulation is indicated by n-alkane distribution patterns, composition of steroids and δ13C of hydrocarbon biomarkers. Microbial communities included heterotrophic bacteria, cyanobacteria, chemoautotrophic bacteria, as well as green sulfur bacteria. Higher inputs of terrigenous organic matter occurred during deposition of the Upper Oligocene units of the Maikop Formation from Angeharan mountains. The terpenoid hydrocarbon composition argues for angiosperm dominated vegetation in the Shamakhy–Gobustan area.High primary bioproductivity resulted in a stratified water column and the accumulation of organic matter rich sediments in the Lower Oligocene units of the Maikop Formation. Organic carbon accumulation during this period occurred in a permanently (salinity-) stratified, mesohaline environment with free H2S in the water column. This is indicated by low pristane/phytane ratios of all sediments (varying from 0.37–0.69), lower methylated-(trimethyltridecyl)chromans ratio in the lower units and their higher contents of aryl isoprenoids and highly branched isoprenoid thiophenes. Subsequently, the depositional environment changed to normal marine conditions with oxygen deficient bottom water. The retreat of the chemocline towards the sediment–water interface and enhanced oxic respiration of OM during deposition of the Upper Oligocene Maikop sediments is proposed.Parallel depth trends in δ13C of total OM, n-alkanes, isoprenoids and steranes argue for changes in the regional carbon cycle, associated with the changing environmental conditions. Increased remineralisation of OM in a more oxygenated water column is suggested to result in low TOC and hydrocarbon contents, as well as 15N enriched total nitrogen of the Upper Oligocene units.  相似文献   

17.
《Organic Geochemistry》1987,11(1):41-51
Carbon isotopic composition, carbon to nitrogen ratios, carbon preference (n-C23 to n-C32), and microscopic examination of selected samples were compared and contrasted as organic matter source indicators. The Orinoco, Nile, and Changjiang deltas were sampled and analyzed. The δ 13C of organic matter increased with distance offshore at all three locations. Organic carbon content decreased seaward on the Orinoco and Changjiang deltas but increased on the Nile delta. C/N ratios decreased regularly with distance offshore on the Orinoco delta, ranged from 10 to 25, and correlated positively with δ 13COM. Estimations of the relative input of marine versus terrestrial organic matter to the sediments was dependent on the parameter analyzed. These discrepancies were primarily due to the definition of end-member compositions and the fraction of the total organic matter that is measured by a given parameter. Multiple-source indicators must be measured and integrated and end-members must be properly defined in order to obtain realistic input estimates.  相似文献   

18.
The geochemical composition of lake bed sediments of a tropical reservoir in Brazil have been investigated. The C, N, P composition showed almost no variation between the different sampling points. All samples contained inorganic phosphorus (IP) ranging from 52 to 70%. The Redfield ratios show that the lake is without significant anthropogenic inputs. Most of the organic matter is composed by higher plants decomposition revealed in the total organic carbon (TOC):nitrogen (N) ratio ranging from 15.4 to 57.2. Also, TOC:organic phosphorus (OP) ranged from 265.3 to 933.6, suggesting that most of the organic matter has terrestrial origin from wood plants. The ratios suggest that most organic matter is influenced by the terrestrial characteristics of the watershed. Furthermore, the relative abundance of n-alkane homologues in the sediments was investigated. All samples have been analyzed for the n-alkanes C8 to C40. The sediments were dominated by n-alkanes C25–C38. It is concluded that n-alkane in sediments mainly come from terrestrial plants, however there is a contribution of submerged aquatic plants, especially in those sites in deeper areas of the lake. On the basis of Paq index the n-alkanes in sediments comes from terrestrial plants, however there is a contribution from emerged/floating plants.The investigated lake seems to be considered as meso to eutrophic. Because of the relatively high primary productivity in the lakes, there is a substantial organic-matter flux to the sediments, which rapidly becomes anoxic. According to the pristine/phytane ratio the sediments represent an anoxic environment with values found between 0.38 and 1.72.  相似文献   

19.
Hydrocarbons and bulk organic matter of two sediment cores (No. 84 and 126, CHAIN 61 cruise) located within the Atlantis II Deep have been analyzed. Although the brines overlying the coring areas were reported to be sterile, microbial inputs and minor terrestrial sources represent the major sedimentary organic material. This input is derived from the upper water column above the brines.Both steroid and triterpenoid hydrocarbons show that extensive acid-catalyzed reactions are occurring in the sediments. In comparison with other hydrothermal (Guaymas Basin) or intrusive systems (Cape Verde Rise), the Atlantis II Deep exhibits a lower degree of thermal maturation. This is easily deduced from the elemental composition of the kerogens and the absence of polynuclear aromatic hydrocarbons of a pyrolytic origin in the bitumen.The lack of carbon number preference among the n-alkanes suggests, especially in the case of the long chain homologs, that the organic matter of Atlantis II Deep sediments has undergone some degree of catagenesis. However, the yields of hydrocarbons are much lower than those observed in other hydrothermal areas. The effect of lower temperature and poor source-rock characteristics appear to be responsible for the differences.  相似文献   

20.
Extractable biomarkers can help elucidate the environment and biota of ancient glaciations, although the method must be applied with care, as glacial sediments have a potential for incorporation of older detrital carbon. In Phanerozoic glacial sediments, the distinct elemental, molecular and isotopic compositions of the terrestrial and marine biomass allow discrimination between primary marine and redeposited terrestrial organic matter. However, as the Proterozoic biosphere was largely microbial and marine, biomarker and isotopic analyses are insufficient for distinguishing primary organic matter from secondary reworked organic matter. Here, we report the combined application of Raman spectroscopy and biomarker analysis to Precambrian glacial sediments, which, together, allows discrimination between mixed pools of organic carbon and provides a promising new approach for rapidly screening Precambrian sediments for immature organic matter amenable to biomarker analysis.  相似文献   

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