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 703 毫秒
1.
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   

2.
Pollen grains from grasses using the C3 and C4 photosynthetic pathways have distinct ranges of δ13C values that may be used to estimate their relative abundance in paleorecords. We evaluated a spooling-wire microcombustion device interfaced with an isotope-ratio mass spectrometer (SWiM-IRMS) for δ13C analysis of individual grass-pollen grains. Pollen from four C3 and four C4 grass species was isolated through micromanipulation and analyzed as single grains suspended in water. A carbon yield greater than the 2σ range of the carbon content of blanks containing only water was used to distinguish samples containing pollen (“pollen present”) from those not containing pollen. This criterion resulted in the exclusion of ∼45% of the 946 samples applied to the wire. The average δ13C values (±1σ) of the remaining samples were −26.9‰ (±6.3‰) and −11.5‰ (±9.6‰) for C3 grasses and C4 grasses, respectively, after blank-correcting the δ13C data. These results suggest that the SWiM-IRMS system can be used to distinguish C3 from C4 grass pollen. The high variability in measured δ13C values is likely caused by a combination of factors. These include natural isotopic variability among individual pollen grains; the relatively poor precision that can be obtained when determining δ13C values of such small samples; and the uncertainty in the magnitude, isotopic composition, and stability of the analytical blank. Nonetheless, high percentages of individual pollen grains were correctly classified as being of either C3 or C4 origin. On average, 90% (range = 78-100%) of pollen grains from C3 grasses had δ13C values more negative than the cutoff threshold of −19.2‰; while 84% (range = 77-90%) of pollen grains from C4 grasses had δ13C values more positive than −19.2‰. Compared with analysis using an elemental analyzer interfaced with an IRMS (EA-IRMS), the number of pollen grains required for δ13C-based evaluation of C3/C4 grass composition is many times lower with the SWiM-IRMS. Additionally, δ13C data from the SWiM-IRMS does not need to be incorporated into a mixing model to derive estimates of the abundance of C3 and C4 grass pollen. Carbon-isotopic analysis of individual grass-pollen grains using the SWiM-IRMS system may help improve our understanding of the evolutionary and ecological significance of grass taxa in the paleorecord.  相似文献   

3.
Surface sediments from an anoxic marine environment, the Upper Basin of the Pettaquamscutt River, Rhode Island, were analyzed for volatile organic compounds in the C1C7 range. The compounds identified included methane, ethane, alkenes (C2C5), carbon disulfide, cyclopentane, 3-methylpentane, methylfuran, aldehydes and ketones. Ethane, methylfuran, and most of the aldehydes and ketones showed maxima at the sediment water interface. Methane levels were very high-10–100 times greater than observed in most other surface sediments examined in this laboratory.  相似文献   

4.
Agricultural grasses cover a major part of the land surface in temperate agro-ecosystems and contribute significantly to the formation of soil organic matter. Crop-derived lipids are assumed to be responsible for fast carbon turnover in soils. Differences in lipid distribution patterns between crops following C3 and C4 photosynthesis pathways have rarely been described, but could be useful for source apportionment of crop-derived input into soils or sediments. The distribution of long chain n-carboxylic acids (C22, C24, C26) reveals significant differences between crop plants following either the C3 or the C4 photosynthetic carbon fixation pathway. The plant compartments leaves, stems and roots of C4 plants contain relatively large proportions (> 40%) of n-C24 carboxylic acid when compared to C3 plants. These reveal larger relative proportions of n-C22 and n-C26 acids, whose relative abundance is subject to change between different plant compartments and during the growing season. The carboxylic acid ratio [CAR = n-C24/(n-C22 + n-C26) carboxylic acids] provides distinct ratios for C4 (> 0.67) and C3 crops (< 0.67) and can thus be used as a molecular marker for the differentiation of crop plant biomass. In combination with the bulk stable carbon isotopic composition (δ13C) the CAR can be used as a tool for the estimation of the C4 derived carbon proportion in soils or sediments.  相似文献   

5.
A suite of 18 oils from the Barrow Island oilfield, Australia, and a non-biodegraded reference oil have been analysed compositionally in order to detail the effect of minor to moderate biodegradation on C5 to C9 hydrocarbons. Carbon isotopic data for individual low molecular weight hydrocarbons were also obtained for six of the oils. The Barrow Island oils came from different production wells, reservoir horizons, and compartments, but have a common source (the Upper Jurassic Dingo Claystone Formation), with some organo-facies differences. Hydrocarbon ratios based on hopanes, steranes, alkylnaphthalenes and alkylphenanthrenes indicate thermal maturities of about 0.8% Rc for most of the oils. The co-occurrence in all the oils of relatively high amounts of 25-norhopanes with C5 to C9 hydrocarbons, aromatic hydrocarbons and cyclic alkanes implies that the oils are the result of multiple charging, with a heavily biodegraded charge being overprinted by fresher and more pristine oil. The later oil charge was itself variably biodegraded, leading to significant compositional variations across the oilfield, which help delineate compartmentalisation. Biodegradation resulted in strong depletion of n-alkanes (>95%) from most of the oils. Benzene and toluene were partially or completely removed from the Barrow Island oils by water washing. However, hydrocarbons with lower water solubility were either not affected by water washing, or water washing had only a minor effect. There are three main controls on the susceptibility to biodegradation of cyclic, branched and aromatic low molecular weight hydrocarbons: carbon skeleton, degree of alkylation, and position of alkylation. Firstly, ring preference ratios at C6 and C7 show that isoalkanes are retained preferentially relative to alkylcyclohexanes, and to some extent alkylcyclopentanes. Dimethylpentanes are substantially more resistant to biodegradation than most dimethylcyclopentanes, but methylhexanes are depleted faster than methylpentanes and dimethylcyclopentanes. For C8 and C9 hydrocarbons, alkylcyclohexanes are more resistant to biodegradation than linear alkanes. Secondly, there is a trend of lower susceptibility to biodegradation with greater alkyl substitution for isoalkanes, alkylcyclohexanes, alkylcyclopentanes and alkylbenzenes. Thirdly, the position of alkylation has a strong control, with adjacent methyl groups reducing the susceptibility of an isomer to biodegradation. 1,2,3-Trimethylbenzene is the most resistant of the C3 alkylbenzene isomers during moderate biodegradation. 2-Methylalkanes are the most susceptible branched alkanes to biodegradation, 3-methylalkanes are the most resistant and 4-methylalkanes have intermediate resistance. Therefore, terminal methyl groups are more prone to bacterial attack compared to mid-chain isomers, and C3 carbon chains are more readily utilised than C2 carbon chains. 1,1-Dimethylcyclopentane and 1,1-dimethylcyclohexane are the most resistant of the alkylcyclohexanes and alkylcyclopentanes to biodegradation. The straight-chained and branched C5–C9 alkanes are isotopically light (depleted in 13C) relative to cycloalkanes and aromatic hydrocarbons. The effects of biodegradation consistently lead to enrichment in 13C for each remaining hydrocarbon, due to preferential removal of 12C. Differences in the rates of biodegradation of low molecular weight hydrocarbons shown by compositional data are also reflected in the level of enrichment in 13C. The carbon isotopic effects of biodegradation show a decreasing level of isotopic enrichments in 13C with increasing molecular weight. This suggests that the kinetic isotope effect associated with biodegradation is site-specific and often related to a terminal carbon, where its impact on the isotopic composition becomes progressively ‘diluted’ with increasing carbon number.  相似文献   

6.
We studied the distribution of organic carbon in rocks of the Bazhenov horizon, a unique object of predominantly biogenic sedimentation in the West Siberian sedimentary basin. The contents of organic carbon in the rocks were determined using the data from 4094 core analyses and core-log relationships derived from 48,500 radioactive- and electrical-log measurements. For the Bazhenov and Tutleima Formations, both approaches gave the same results. The average content of organic carbon in the rocks is 7.7%. These data were used to compile a detailed map of the distribution of organic carbon contents in sedimentary rocks of the basin. It was shown that the average organic carbon content in the rocks increases from 2-4% on the periphery of the basin to 10-12% in its central, deepest part. The distribution of Corg values in the basin is highly asymmetric. The highest Corg values are observed in the southwestern part of the basin interior, where beds with > 10% Corg range in thickness from 5 to 12-15 m. In sections, the highest Corg values are observed in their middle and upper parts, composed predominantly of silicites and mixtites enriched in biogenic silica.  相似文献   

7.
All of the major deep-water sedimentary provinces of the Gulf of Mexico were sampled with 48 piston cores, representative of the late Quaternary. The amount (per cent) and δ5C13 of the organic carbon in the sediment was measured at intervals within each core.Graphs of δC13 versus depth for each core give an indication of the sedimentological history of the Gulf. They show the extent of terrestrial influence on the Gulf during the late Pleistocene.Changes in δC13 of up to 6.0%.(from ~ ?19%.to ?25%. vs NBS-20) were measured across the Pleistocene-Holocene boundary in cores from the abyssal plain. These changes are consistent with a model wherein varying amounts of land-derived organic carbon were transported to the Gulf basin during glacial periods.By comparing graphs for cores from different areas, it was concluded that the major parameter affecting the δC13 values of organic carbon from marine sediments is the relative amount of terrestrial material present in the sediment. The maximum possible effect of the Pleistocene-Holocene temperature change in the Gulf was determined to be ~1.0%, if such an effect occurs at all.  相似文献   

8.
The δ13C and δ18O values of well-preserved carbonate rhizoliths (CRs) provide detailed insights into changes in the abundance of C3 and C4 plants in response to approximately decadal-scale changes in growing-season climate. We performed stable isotope analyses on 35-40 CRs sampled at 1-cm intervals from an 18-cm-thick paleosol formed in southern Illinois during Wisconsin interstadial 2. Minimum δ13C values show little variation with depth, whereas maximum values vary dramatically, and average values show noticeable variability; maximum δ18O values vary less than the minimum δ18O values. These findings indicate that a diverse and stable C3 flora with a limited number of C4 grass species prevailed during this interval, and suggest that the maximum growing-season temperatures were relatively stable, but minimum growing-season temperatures varied considerably. Two general patterns characterize the relationships between the δ13C and δ18O values obtained from the 1-cm samples. In some cases, low δ13C values correspond to low δ18O values and high δ13C values correspond to high δ18O values, suggesting that cooler growing-season temperatures favored C3 and warmer growing-season temperatures favored C4 plants. In other cases, low δ13C values correspond to high δ18O values, likely suggesting that wetter growing-season conditions were favorable to C3 plants. The high density of well-preserved CRs in this paleosol provides a unique opportunity to study detailed ecological responses to high-resolution variability in growing-season climate.  相似文献   

9.
Carbon isotope compositions of both sedimentary carbonate and organic matter can be used as key proxies of the global carbon cycle and of its evolution through time,as long as they are acquired from waters where the dissolved inorganic carbon(DIC)is in isotope equilibrium with the atmospheric CO2.However,in shallow water platforms and epeiric settings,the influence of local to regional parameters on carbon cycling may lead to DIG isotope variations unrelated to the global carbon cycle.This may be especially true for the terminal Neoproterozoic,when Gondwana assembly isolated waters masses from the global ocean,and extreme positive and negative carbon isotope excursions are recorded,potentially decoupled from global signals.To improve our understanding on the type of information recorded by these excursions,we investigate the pairedδ^13Ccarb andδ^13Corg evolution for an increasingly restricted late Ediacaran-Cambrian foreland system in the West Gondwana interior:the basal Bambui Group.This succession represents a 1~(st)-order sedimentary sequence and records two majorδ^13Ccarb excursions in its two lowermost lower-rank sequences.The basal cap carbonate interval at the base of the first sequence,deposited when the basin was connected to the ocean,hosts antithetical negative and positive excursions forδ^13Ccarb andδ^13Corg,respectively,resulting inΔ^13C values lower than 25‰.From the top of the basal sequence upwards,an extremely positiveδ^13Ccarb excursion is coupled toδ^13Corg,reaching values of+14‰and-14‰,respectively.This positive excursion represents a remarkable basin-wide carbon isotope feature of the Bambui Group that occurs with only minor changes inΔ^13C values,suggesting change in the DIC isotope composition.We argue that this regional isotopic excursion is related to a disconnection between the intrabasinal and the global carbon cycles.This extreme carbon isotope excursion may have been a product of a disequilibria between the basin DIC and atmospheric CO2 induced by an active methanogenesis,favored by the basin restriction.The drawdown of sulfate reservoir by microbial sulfate reduction in a poorly ventilated and dominantly anoxic basin would have triggered methanogenesis and ultimately methane escape to the atmosphere,resulting in a^13C-enriched DIC influenced by methanogenic CO2.Isolated basins in the interior of the Gondwana supercontinent may have represented a significant source of methane inputs to the atmosphere,potentially affecting both the global carbon cycle and the climate.  相似文献   

10.
The δC13 value for sedimentary organic carbon in four estuaries of the Gulf of Mexico increases with radial distance from the river mouth. Mass balance calculations indicate that terrestrial organic carbon is limited to sediments within a relatively short distance from the river mouth. This distance is a function of the discharge rate of the river. For the Mississippi River, terrestrial organic carbon is limited to sediments within 69 km of the mouth of Pass à Loutre and 61 km of South Pass. These data indicate that the low δC13 (< ?22%.) values reported for Pleistocene sediments in the Gulf of Mexico may be the result of factors in addition to the postulated large influx of terrestrial organic carbon.  相似文献   

11.
Orca Basin is a highly reducing basin on the slope of the Gulf of Mexico. Stable carbon isotope ratios and total organic carbon percentages were determined for two cores within the basin and one control core outside the basin. The results show that the organic carbon content of the basin cores is consistently 2–3 times greater than that of the control core. The Pleistocene-Holocene boundary, indicated by a break in the δ13C depth profile, occurs at a greater sediment depth in the basin cores than in the control core. A small sampling interval has made it possible to detect an unexplained fine structure in the δ13C profile not previously observed.  相似文献   

12.
文章利用黄土高原西缘代表性的塬堡剖面有机碳同位素数据,估算了末次冰期以来地表植被中C3/C4植 物的相对丰度,指示出研究区域末次冰期几乎为纯粹的C3植物,而全新世为C3植物占优势的C3和C4混合植被类 型。温度是控制中国黄土高原C4植物是否发生的关键性气候因素,末次冰期向全新世转化过程中存在的某“阈值 温度”控制了两种植被类型的存在。全新世土壤有机碳同位素偏正于末次冰期,符合前人研究得到的认识。末次 冰期间冰段(MIS3)至盛冰期,土壤有机碳同位素为偏正变化趋势,符合现代C3植物本身随气候条件改变的碳同位 素组成变化。研究表明,利用黄土-古土壤有机碳同位素进行古气候变化研究,不能只将有机碳同位素简单的解 释为C3/C4植物相对丰度的变化,在单一植被类型下,还需要考虑植物本身碳同位素组成随气候条件的变化;另外, 研究还说明,我国黄土高原不同地区同时段土壤有机碳同位素值可以不同,其变化可以不具有相同的趋势,因此, 简单将有机碳同位素偏正归因于夏季风增强是值得商榷的。  相似文献   

13.
The carbon stable isotopic value of dissolved inorganic carbon (δ13CDIC) was measured over several years at different depths in the water column in six carbonate-precipitating temperate lakes. δ13CDIC behavior in three of these lakes departed from the conventional model wherein epilimnetic waters are seasonally enriched relative to all hypolimnetic waters, and in general δ13CDIC values in the water column were not readily correlated to parameters such as lake stratification, algal productivity, hydraulic residence time, or water chemistry. Additionally, the processes implicated in generating the δ13CDIC values of individual lakes differ between lakes with similar δ13CDIC compositions. Each lake thus initially appears idiosyncratic, but when the effects of carbonate mineral equilibria, microbial activity, and lake residence time are viewed in terms of the magnitude of distinct DIC pools and fluxes in stratified lakes, generalizations can be made that allow lakes to be grouped by δ13CDIC behavior. We recognize three modes in the relationship between δ13CDIC values and DIC concentration ([DIC]) of individual lakes: (A) δ13CDIC values decreasing with increasing [DIC]; (B) δ13CDIC values increasing with increasing [DIC]; (C) δ13CDIC values decreasing with increasing [DIC] but increasing again at the highest [DIC]. This approach is useful both in understanding δ13CDIC dynamics in modern hardwater lakes and in reconstructing the environmental changes recorded by sedimentary δ13C components in the lacustrine paleorecord.  相似文献   

14.
The Neoproterozoic Doushantuo Formation on the Yangtze Platform, South China, documents a sedimentary succession with different sedimentary facies from carbonate platform to slope and to deep sea basin, and hosts one of the world-class phosphorite deposits. In these strata, exquisitely preserved fossils have been discovered： the Weng＇an biota. This study presents carbon isotope geochemistry which is associated paired carbonate and organic matter from the Weng＇an section of a carbonate platform （shelf of the Yangtze Platform, Guizhou Province） from the Songtao section and Nanming section of a transition belt （slope of the Yangtze Platform, Guizhou Province） and from the Yanwutan section （basin area of the Yangtze Platform, Hunan Province）. Environmental variations and bio-events on the Yangtze Platform during the Late Neoproterozoic and their causal relationship are discussed. Negative carbon isotope values for carbonate and organic carbon （mean δ^13Corg = -35.0‰） from the uppermost Nantuo Formation are followed by an overall increase in δ^13C up-section. Carbon isotope values vary between -9.9‰ and 3.6‰ for carbonate and between -35.6‰ and -21.5‰ for organic carbon, respectively. Heavier δ^13Ccarb values suggest an increase in organic carbon burial, possibly related to increasing productivity （such as the Weng＇an biota）. The δ^13C values of the sediments from the Doushantuo Formation decreased from the platform via the slope to basin, reflecting a reduced environment with minor dissolved inorganic carbon possibly due to a lower primary productivity. It is deduced that the classical upwelling process, the stratification structure and the hydrothermal eruption are principally important mechanisms to interpret the carbon isotopic compositions of the sediments from the Doushantuo Formation.  相似文献   

15.
The distribution of organic carbon in the Bazhenov horizon rocks of the western Siberian sedimentary basin is investigated. The organic carbon concentration in rocks is estimated by the results of core analyses (4094 core analyses) and by the calculations of the core-log data correlations (48 500 measurements) according to the data of radiation and electrical loggings. The average content of organic carbon in the rocks of the Bazhenov and Tutleim (lower subformation) formation is 7.7%. The map of organic carbon concentrations in the sedimentary rocks of the basin is constructed. In the basin, Corg is distributed asymmetrically. The region of maximum Corg concentrations occupies the southwestern part of the internal area of the sedimentary basin. Silicites and biogene silica-enriched mixtites are enriched with organic matter most of all.  相似文献   

16.
In situ carbon flux measurements and calculated burial rates are utilized to construct an organic carbon budget for the upper meter of sediment at a single station in Cape Lookout Bight, a small marine basin located on the Outer Banks of North Carolina, U.S.A. (34°37′N, 76°33′W). Of 149 ± 20 mole · m?2 · yr?1 of total organic carbon deposited, 35.6 ± 5.2 mole · m?2 · yr?1 is recycled to overlying waters, 84 ± 18% as ∑CO2 and 16 ± 8% as CH4. Approximately 68 ± 20% of the upward carbon flux is supported by sulfate reduction while 32 ± 16% takes place as the result of underlying methanogenesis. Measured ∑CO2 and CH4 sediment-water fluxes range seasonally from 1900–6300 and 50–2500 μmole · m?2 · hr?1 respectively.The mean residence time of metabolizable organic carbon in the upper 80 cm of sediment is approximately four months with greater than 98% of the calculated total remineralization taking place within three years. In spite of large upward fluxes of methane, larger molecules derived from metabolizable sedimentary organic carbon appear to be the dominant reductants for dissolved sulfate.  相似文献   

17.
Carbon isotope values of 260 Precambrian limestones and dolomites (most of them being substantially unaltered) have yielded an overall mean of δ 13C = +0.4 ± 2.7‰ vs. PDB; the corresponding oxygen values average at δ 13O = +20.0 ± 4.2‰ vs. SMOW. Like the overall mean, the δ 13C values furnished by individual carbonate occurrences are, as a rule, fairly “modern” and almost constant as from the very beginning of the sedimentary record. A remarkable exception are the “heavy” dolomites of the Middle Precambrian Lomagundi Group, Rhodesia, with δ 13C = +9.4 ± 2.0‰ vs. PDB. As a result of our measurements, the sporadic occurrence in the geological past of anomalously heavy carbonates seems to be established.The approximate constancy around zero per mill of the δ 13C values of marine carbonates through geologic time would imply a corresponding constancy of the relative proportion of organic carbon in the total sedimentary carbon reservoir since about 3.3 · 109 y ago (with Corg/Ctotal ? 0.2). Utilizing this ratio and current models for the accumulation of the sedimentary mass as a function of time, we get a reasonable approximation for the absolute quantity of organic carbon buried in sediments and, accordingly, of photosynthetic oxygen released. Within the constraints of our model (based on a terrestrial degassing constant λ = 1.16 · 10?9 y?1) close to 80% of the amount of oxygen contained in the present oxygen budget should have been released prior to 3 · 109 y ago. Since geological evidence indicates an O2-deficient environment during the Early and most parts of the Middle Precambrian, there is reason to believe that the distribution of this oxygen between the “bound” and the “molecular” reservoir was different from that of today (with effective O2-consuming reactions bringing about an instantaneous transfer to the crust of any molecular oxygen released). Accordingly, the amount of Corg in the ancient sedimentary reservoir as derived from our isotope data is just a measure of the gross amount of photosynthetic oxygen produced, withholding any information as to how this oxygen was partitioned between the principal geochemical reservoirs. As a whole, the carbon isotope data accrued provide evidence of an extremely early origin of life on Earth since the impact of organic carbon on the geochemical carbon cycle can be traced back to almost 3.5 · 109y.  相似文献   

18.
This study investigated the geochemical features of the lower Paleozoic strata of Yaerdang Mountain outcrop along with the core samples from well TD2∈ in the eastern Tarim Basin,NW China.The total organic carbon abundance,hydrocarbon-generating precursor biospecies,and stable isotope ratios of organics and carbonate(δ~(13)C_(ker),δ~(13)C_(carb) and δ~(18)O_(carb)) were comprehensively studied for their possible correlative constraints during sedimentary evolution.The results revealed that the δ~(13)C_(ker)(VPDB) of Cambrian kerogens along the outcrop section varied from-34.6‰ to-28.4‰,indicating an increasing tendency from the lower Cambrian to the upper Cambrian.This was on the whole accompanied by the variation in the δ~(13)C_(carb) and δ~(18)O_(carb) along the profile,which might be associated with the changes in the sea level and also in the compositional variation of benthic and planktonic biomass.The large variation in the stable carbon isotope ratios up to 6‰ along the outcrop section reflected the heterogeneity of the Cambrian source rocks from the eastern Tarim Basin.Hence,the ~(13)C-enriched crude oils from well TD2∈might have been derived from a localized stratum of Cambrian source rocks.The results from this study showed the possibility of multiple source kitchens in the Cambrian-lower Ordovician portion of Tarim Basin.  相似文献   

19.
One hundred and twenty-four carbonate samples from the meta-sedimentary sequence of the 3.7 × 109 yr old Isua supracrustal belt (W-Greenland) have yielded a δ13Ccarb average of ?2.5 ± 1.7%. vs PDB and a δ18Ocarb average of +13.0 ± 2.5%. vs SMOW. The oxygen mean comes fairly close to the averages of other early Precambrian carbonates. The carbon average, however, is some 2%. more negative than those of younger marine carbonates. In terms of a simple terrestrial 13C mass balance, if δ13Ccarb values are original sedimentary values, this more negative δ13C average would imply a considerably smaller CorgCcarb ratio in the sedimentary shell during Isua times, and would thus support the concept of a gradual buildup of a sedimentary reservoir of organic carbon during the early history of the Earth. Since, however, the Isua supracrustal rocks have experienced amphibolite-grade metamorphism, which in other areas has been shown to lower δ13Ccarb values, it is most likely that the original values of these rocks were approx 0%.. This indicates that Corx and Ccarb were present in the ancient carbon reservoir in about ‘modern’ proportions. Unless this early stabilization of the terrestrial carbon cycle in terms of a constant partitioning of carbon between the reduced and oxidized species is shown to have been caused by some inorganic geochemical process, a considerably earlier start of chemical evolution and spontaneous generation of life must be considered than is presently accepted.  相似文献   

20.
Carbon isotope studies have been carried out on marine Phanerozoic sediments of the Williston Basin, North America. Special attention was given to the recognition of systematic variations with age.δ 13C measurements on the carbonate fraction show a 3%0 depletion from the Cambrian to the Mississippian and a 1–2%0 enrichment to the Jurassic. Both the sign of these displacements and a good correlation with the organic carbon content suggest that real variations in the rate of photosynthesis may have been the driving force for these changes with age.Because of the large isotopic heterogeneities in the organic biomass, systematic fluctuations with age in the δ 13C-values of the total organic carbon record are hard to prove. Nevertheless, a significant 3%0 depletion was observed from the Devonian to the end of the Carboniferous. This depletion seems to occur on a worldwide scale. It is therefore proposed that a rise in the rate of photosynthesis as a consequence of the colonization of the continents by higher plants is the global cause of this displacement in the isotope record of the total organic carbon.The bitumen fraction does not show any systematic isotope variations with age.Comparison of coexisting δ 13Corg?δ 13Cbit pairs demonstrates that during the Ordovician-Mississippian time period no significant (> 1%0) differences in the isotope values of these two organic carbon sources can be observed. In contrast the bitumen fraction is depleted in 13C as compared to the total organic carbon in the Cambrian as well as in the Pennsylvanian-Cretaceous time interval. Several parameters, i.e. the depth of burial of these sediments, the 12(pristane/n-C17 + phytane/n-C18) ratio and the n-alkane distribution pattern support the theory that the rank of the organic matter may be responsible for the observed isotopic pattern.  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