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1.
Despite the great extent of the Brazilian coast, there are very few studies on the marine radiocarbon reservoir correction local offset (ΔR) for this region.In the present study, we used marine shells from the malacological collection of the National Museum of Brazil to obtain values of ΔR for different locations on the Brazilian coast. According to the museum records, the mollusks were collected alive from the coasts of Rio de Janeiro, Rio Grande do Sul, São Paulo and Bahia, prior to the 14C bomb-peak. The exact year of collection for each shell is known.The samples were chemically prepared and measured at the Radiocarbon Laboratory of the Universidade Federal Fluminense (LAC-UFF) in Brazil. The conventional ages were calibrated using the Marine13 curve and the ΔR values were calculated using the OxCal software. The values range from 17 ± 56 14C yr in São José do Norte, Rio Grande do Sul to 96 ± 48 14C yr in Cabo Frio, Rio de Janeiro.  相似文献   

2.
Although 1-alkyl-2,3,6-trimethylbenzenes and a high relative amount of 1,2,3,4-tetramethylbenzene have been detected in marine oils and oil asphaltenes from Tabei uplift in the Tarim Basin, their bio-logical sources are not determined. This paper deals with the molecular characteristics of typical ma-rine oil asphaltenes from Tabei and Tazhong uplift in the Tarim Basin and the stable carbon isotopic signatures of individual compounds in the pyrolysates of these asphaltenes using flash pyrolysis-gas chromatograph-mass spectrometer (PY-GC-MS) and gas chromatograph-stable isotope ratio mass spectrometer (GC-C-IRMS), respectively. Relatively abundant 1,2,3,4-tetramethylbenzene is detected in the pyrolysates of these marine oil asphaltenes from the Tarim Basin. δ 13C values of 1,2,3,4-tetrame-thylbenzene in the pyrolysates of oil asphaltenes vary from-19.6‰ to-24.0‰, while those of n-alkanes in the pyrolysates show a range from-33.2‰ to-35.1‰. The 1,2,3,4-tetramethylbenzene in the pyro-lysates of oil asphaltenes proves to be significantly enriched in 13C relative to n-alkanes in the pyro-lysates and oil asphaltenes by 10.8‰―15.2‰ and 8.4‰―13.4‰, respectively. This result indicates a contribution from photosynthetic green sulfur bacteria Chlorobiaceae to relatively abundant 1,2,3,4-tetramethylbenzene in marine oil asphaltenes from the Tarim Basin. Hence, it can be speculated that the source of most marine oil asphaltenes from the Tarim Basin was formed in a strongly reducing water body enriched in H2S under euxinic conditions.  相似文献   

3.
Structural aspects of humic substances (HSs) in marine waters of Engaño Bay (Atlantic Ocean) and water from the Chubut River (Patagonia, Argentina) were compared. The HSs were isolated, purified, and analyzed using a multiple-method approach for structural characterization: elemental analysis, nuclear magnetic resonance (13C and 1H NMR), infrared spectroscopy (FTIR), UV-visible absorption and fluorescence. Similarities between the marine and freshwater components were evaluated on the basis of N and O contents, H/C and C/N atomic ratios, infrared bands from nitrogen-containing and carboxylic groups, percentage of functional groups obtained from NMR spectra, spectral slope coefficient of absorption spectra, absorbance ratios at 250 and 365 nm (E 2/E 3), aromaticity, excitation–emission matrices and fluorescence quantum yield. Both the Engaño Bay and Chubut River waters have HSs that are mainly composed of fulvic acids (FAs); although they are very similar, they may be distinguished from one another. Similarities include the predominance of aliphatic carbon content (low aromatic content); however, the water bodies differed in their content of proteins and carboxylic acids. The Engaño Bay FAs have mainly an aquatic origin; although the Chubut River FAs suggest a similar aquagenic origin, there is also evidence of contributions from pedogenic FAs.  相似文献   

4.
Radiocarbon: A chronological tool for the recent past   总被引：2，自引：2，他引：0  
The past few hundred years have seen large fluctuations in atmospheric 14C concentration. In part, these have been the result of natural factors, including the climatic changes of the Little Ice Age, and the Spörer and Maunder solar activity minima. In addition, however, changes in human activity since the middle of the 19th century have released 14C-free CO2 to the atmosphere. Moreover, between c. 1955 and c. 1963, atmospheric nuclear weapon testing resulted in a dramatic increase in the concentration of 14C in the atmosphere. This was followed by a significant decrease in atmospheric 14C as restrictions on nuclear weapon testing began to take effect and as rapid exchange occurred between the atmosphere and other carbon reservoirs. The large fluctuations in atmospheric 14C that occurred prior to 1955 mean that a single radiocarbon date may yield an imprecise calibrated age consisting of several possible age ranges. This difficulty may be overcome by obtaining a series of 14C dates from a sequence and either wiggle-matching these dates to a radiocarbon calibration curve or using additional information on dated materials and their surrounding environment to narrow the calibrated age ranges associated with each 14C date. For the period since 1955 (the bomb-pulse period), significant differences in atmospheric 14C levels between consecutive years offer the possibility of dating recent samples with a resolution of from one to a few years. These approaches to dating the recent past are illustrated using examples from peats, lake and salt marsh sediments, tree rings, marine organisms and speleothems.  相似文献   

5.
Kinetic experiments of gas generation for typical samples of marine gas precursors including low-maturity kerogen, residual kerogen and oil as well as dispersed liquid hydrocarbon (DLH) in source rocks were performed by closed system, and the evolution trends of molecular and isotopic compositions of natural gases from different precursors against the maturity (R 0%) at laboratory conditions were analyzed. Several diagrams of gas origin were calibrated by using the experimental data. A diagram based on the ratio of normal and isomerous butane and pentane (i/nC4 ? i/nC5) was proposed and used to identify the origins of the typical marine natural gases in the Sichuan Basin and the Tarim Basin, China. And the maturities of natural gases were estimated by using the statistical relationships between the gaseous molecular carbon isotopic data and maturities (δ13C-R 0%) with different origins. The results indicate that the molecular and isotopic compositions of simulated gases from different precursors are different from each other. For example, the dryness index of the oil-cracking gas is the lowest; the dryness indices of gases from DLH and kerogen in closed system are almost the same; and the dryness index of gases from residual kerogen is extremely high, indicating that the kerogen gases are very dry; the contents of non-hydrocarbon gases in kerogen-cracking gases are far higher than those in oil-cracking and DLH-cracking gases. The molecular carbon isotopes of oil-cracking gases are the lightest, those of kerogen in closed system and GLH-cracking gases are the second lightest, and those of cracking gases from residual kerogen are the heaviest. The calibration results indicate that the diagrams of In(C1/C2)-In(C2/C3) and δ4 3C2-δ4 3C3-In(C2/C3) can discriminate primary and secondary cracking gases, but cannot be used to identify gas origin sources, while the diagram of i/nC4 ? i/nC5 can differentiate the gases from different precursors. The application results of these diagrams show that gas mixtures extensively exist in China, which involved the gases from multiple precursors and those from different maturity stages. For example, marine gases in the Sichuan Basin involve the mixture of oil-cracking gases and high-over-maturated kerogen gases, while those in the Tarim Basin involve not only the mixture of gases from multiple precursors, but also those from different maturity gases and post-reservoir alternations such as oxidized degradation and gas intrusion processes.  相似文献   

6.
《Marine pollution bulletin》2009,58(6-12):403-408
Laboratory experiments were carried out to investigate the adsorption behaviour of dibutyl phthalate (DBP) on marine sediments collected from five different sites in Victoria Harbour, Hong Kong. DBP adsorption can be well described by the Langmuir isotherm. The maximum DBP adsorption capacity (Qmax) of the marine sediments ranges from 53 to 79 mg g−1, which has a positive correlation with their organic content. Around 90% of the organic can be removed from the sediments with treatment by H2O2 oxidation, and the Qmax then decreases to a range between 13 and 22 mg g−1. The black carbon content of the sediments has a much greater DBP adsorption capacity than does the natural organic matter of the sediments. The amount of DBP adsorbed on the sediments increases as the salinity of the marine water increases.  相似文献   

7.
Belemnite guards of Cretaceous and Jurassic age were found to contain varying amounts of quartz deposited both on the external surface and inside the rostrum. The oxygen isotopic composition of coexisting carbonate, quartz and phosphate from the same rostrum was measured according to well-established techniques. None of these compounds showed isotopic values in equilibrium with one another. Assuming δ18O values of the diagenetic water within the range of meteoric waters, the δ18O(SiO2) yield temperatures in agreement with the apparent secondary origin of this phase. The δ18O(CO32−) range, with a certain continuity, between −10.8 and +0.97 PDB-1 with most of the intermediate values being within the range of the carbonate isotopic values of Mesozoic fossils. The most positive isotopic results obtained from phosphate are close to +23/+24‰ (V-SMOW). They can hardly be related to a secondary origin of the phosphate, or to the presence of diagenetic effects, since these results are among the most positive ever measured on phosphate. As far as we know there is no widespread diagenetic process determining an 18O enrichment of phosphate. The very low concentration of phosphate did not allow the determination of its mineralogical composition. All the available δ18O(PO43−) values from belemnite and non-belemnite fossils of marine origin of Tertiary and Mesozoic age are reported along with the newly measured belemnites. The following conclusions may be drawn from the data reported: (1) the pristine oxygen isotope composition of fossil marine organisms (either carbonate or phosphate) may easily undergo fairly large changes because of oxygen isotope exchange processes with diagenetic water; this process is apparent even in the case of geologically recent fossils; (2) the δ18O(PO43−) of belemnite rostra seems to be, at least in the case of the most positive results, in isotopic equilibrium with environmental water because of the similarity between the results from Cretaceous belemnites and the results from Cretaceous and Lower Tertiary pelecypods and fish teeth; 3) if so, the only feasible interpretation that can be suggested for the 18O enriched data is the possibility of a relatively large variation of the oxygen isotopic composition of ocean paleowater from Jurassic to recent time.  相似文献   

8.
At two locations in the Atlantic Ocean (DSDP Sites 367 and 530) early to middle Cretaceous organic-carbon-rich beds (“black shales”) were found to have significantly lower δ15N values (lower15N/14N ratios) than adjacent organic-carbon-poor beds (white limestones or green claystones). While these lithologies are of marine origin, the black strata in particular have °15N values that are significantly lower than those previously found in the marine sediment record and most contemporary marine nitrogen pools. In contrast, black, organic-carbon-rich beds at a third site (DSDP Site 603) contain predominantly terrestrial organic matter and have C- and N-isotopic compositions similar to organic matter of modern terrestrial origin.The recurring15N depletion in the marine-derived Cretaceous sequences prove that the nitrogen they contain is the end result of an episodic and atypical biogeochemistry. Existing isotopic and other data indicate that the low15N relative abundance is the consequence of pelagic rather than post-depositional processes. Reduced ocean circulation, increased denitrification, and, hence, reduced euphotic zone nitrate availability may have led to Cretaceous phytoplankton assemblages that were periodically dominated by N2-fixing blue-green algae, a possible source of this sediment15N-depletion. Lack of parallel isotopic shifts in Cretaceous terrestrially-derived nitrogen (Site 603) argues that the above change in nitrogen cycling during this period did not extend beyond the marine environment.  相似文献   

9.
To assess the environmental perturbation induced by the impact event that marks the Cretaceous–Tertiary (K–T) boundary, concentrations and isotopic compositions of bulk organic carbon were determined in sedimentary rocks that span the terrestrial K–T boundary at Dogie Creek, Montana, and Brownie Butte, Wyoming in the Western Interior of the United States. The boundary clays at both sites are not bounded by coals. Although coals consist mainly of organic matter derived from plant tissue, siliceous sedimentary rocks, such as shale and clay, may contain organic matter derived from microbiota as well as plants. Coals record δ13C values of plant-derived organic matter, reflecting the δ13C value of atmospheric CO2, whereas siliceous sedimentary rocks record the δ13C values of organic matter derived from plants and microbiota. The microbiota δ13C value reflects not only the δ13C value of atmospheric CO2, but also biological productivity. Therefore, the siliceous rocks from these sites yields information that differs from that obtained previously from coal beds.Across the freshwater K–T boundary at Brownie Butte, the δ13C values decrease by 2.6‰ (from − 26.15‰ below the boundary clay to − 28.78‰ above the boundary clay), similar to the trend in carbonate at marine K–T sites. This means that the organic δ13C values reflect the variation of δ13C of atmospheric CO2, which is in equilibrium with carbon isotopes at the ocean surface. Although a decrease in δ13C values is observed across the K–T boundary at Dogie Creek (from − 25.32‰ below the boundary clay to − 26.11‰ above the boundary clay), the degree of δ13C-decrease at Dogie Creek is smaller than that at Brownie Butte and that for marine carbonate.About 2‰ decrease in δ13C of atmospheric CO2 was expected from the δ13C variation of marine carbonate at the K–T boundary. This δ13C-decrease of atmospheric CO2 should affect the δ13C values of organic matter derived from plant tissue. As such a decrease in δ13C value was not observed at Dogie Creek, a process that compensates the δ13C-decrease of atmospheric CO2 should be involved. For example, the enhanced contribution of 13C-enriched organic matter derived from algae in a high-productivity environment could be responsible. The δ13C values of algal organic matter become higher than, and thus distinguishable from, those of plant organic matter in situations with high productivity, where dissolved HCO3− becomes an important carbon source, as well as dissolved CO2. As the δ13C-decrease of atmospheric CO2 reflected a reduction of marine productivity, the compensation of the δ13C decrease by the enhanced activity of the terrestrial microbiota means that the microbiota at freshwater environment recovered more rapidly than those in the marine environment.A distinct positive δ13C excursion of 2‰ in the K–T boundary clays is superimposed on the overall decreasing trend at Dogie Creek; this coincides with an increase in the content of organic carbon. We conclude that the K–T boundary clays include 13C-enriched organic matter derived from highly productive algae. Such a high biological productivity was induced by phenomena resulting from the K–T impact, such as nitrogen fertilization and/or eutrophication induced by enhanced sulfide formation. The high productivity recorded in the K–T boundary clays means that the freshwater environments (in contrast to marine environments) recovered rapidly enough to almost immediately (within 10 yr) respond to the impact-related environmental perturbations.  相似文献   

10.
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11.
Luminescence dating has long been used for chronological constraints on marine sediments due to the ubiquitous dating materials (quartz and feldspar grains) and its applicability over a relatively long time range. However, one of the main difficulties in luminescence dating on marine sediments is partial bleaching, which causes age overestimations. Especially, partial bleaching is typically difficult to be detected in the fine grain fraction (FG) of marine sediments. The recently developed feldspar post-IR IRSL (pIRIR) protocol can detect non-fading signals and thus avoid feldspar signal instability. In the current study, fine grains were extracted from a gravity core in the northern Sea of Japan, and the aim is to test the feasibility of using different luminescence signals with various bleaching rates to explore the bleaching conditions of fine grain fraction in marine sediments. The results suggest that the quartz OSL signal and polymineral pIRIR signals at stimulation temperatures of 150 °C and 225 °C (pIRIR150 and pIRIR225) of FG were well bleached prior to deposition. The OSL ages were used to establish a chronology for this sedimentary core and the resulting age-depth relationship is self-consistent and comparable with radiocarbon dates. We conclude that different luminescence signals with various bleaching rates can be used to test the bleaching conditions of fine grain fraction in marine sediments; and the luminescence dating can be applied to marine sediments with great potential.  相似文献   

12.
Non-dispersive infrared(NDIR) and cavity ring-down spectroscopy(CRDS) CO_2 analyzers use 12CO_2 isotopologue absorption lines and are insensitive to all or part of other CO_2-related isotopologues. This may produce biases in CO_2 mole fraction measurements of a sample if its carbon isotopic composition deviates from that of the standard gases being used. To evaluate and compare the effects of carbon isotopic composition on NDIR and CRDS CO_2 analyzers, we prepared three test sample air cylinders with varying carbon isotopic abundances and calibrated them against five standard cylinders with ambient carbon isotopic composition using CRDS and NDIR systems. We found that the CO_2 mole fractions of the sample cylinders measured by G1301(CRDS) were in good agreement with those measured by Lo Flo(NDIR). The CO_2 values measured by both instruments were higher than that of a CO_2 isotope measured by G2201i(CRDS) analyzer for a test cylinder with depleted carbon isotopic composition δ~(13)C =-36.828‰, whereas no obvious difference was found for other two test cylinders with δ~(13)C=-8.630‰ and δ~(13)C=-15.380‰, respectively. According to the theoretical and experimental results, we concluded that the total CO_2 mole fractions of samples with depleted isotopic compositions can be corrected on the basis of their 12CO_2 values calibrated by standard gases using Lo Flo and G1301 if the δ~(13)C and δ18O values are known.  相似文献   

13.
《Continental Shelf Research》2007,27(3-4):560-582
The first part of this paper presents a review of the problems that constrain the reliability of radiocarbon-based age models with particular focus on those used to underpin marine records. The reasons why radiocarbon data-sets need to be much more comprehensive than has been the norm hitherto, and why age models should be based on calibrated data only, are outlined. The complexity of the probability structure of calibrated radiocarbon data and the advantages of a Bayesian statistical approach for constructing calibrated age models are illustrated. The second part of the paper tests the potential for reducing the uncertainties that constrain radiocarbon-based age models using tephrostratigraphy. Fine (distal) ash layers of Holocene age preserved in Adriatic prodelta sediments are analysed geochemically and compared to tephras preserved in the Lago Grande di Monticchio site in southern Italy. The Monticchio tephras have been dated both by radiocarbon and varve chronology. The importance of basing such comparisons on standardised geochemical and robust statistical procedures is stressed. In this instance, both the Adriatic and Monticchio geochemical measurements are based on wavelength dispersive spectrometry, while discriminant function analysis is employed for statistical comparisons. Using this approach, the ages of some of the Adriatic marine ash layers could be estimated in Monticchio varve years, circumventing some of the uncertainty of radiocarbon-based age models introduced by marine reservoir effects. Fine (distal) ash layers are more widespread and better preserved in Mediterranean marine sequences than realised hitherto and may offer much wider potential for refining the dating and correlation of Mediterranean marine sequences as well as marine-land correlations.  相似文献   

14.
The calibration of marine 14C dates requires the incorporation of regionally specific marine reservoir offsets known as ΔR, essential for accurate and meaningful inter-archive comparisons. Revised, regional ΔR (‘ΔRR’) values for the Barents Sea are presented for molluscs and cetaceans for the two latest iterations of the marine calibration curve, based on previously published pre-bomb live-collected and radiocarbon-dated samples (‘ΔRL’; molluscs: n = 16; cetaceans: n = 18). Molluscan ΔRR, determined for four broad regional oceanographic settings, are: western Svalbard (including Bjørnøya), −61 ± 37 14C yrs (Marine20), 94 ± 38 14C yrs (Marine13); Franz Josef Land, −277 ± 57 14C yrs (Marine20), −122 ± 38 14C yrs (Marine13); Novaya Zemlya, −156 ± 73 14C yrs (Marine20), 0 ± 76 14C yrs (Marine13); northern Norway, −86 ± 39 14C yrs (Marine20), 74 ± 24 14C yrs (Marine13). Molluscan ΔRR values are considered applicable to other marine carbonate materials (e.g., foraminifera, ostracods). Cetacean ΔRR are determined for toothed (n = 10) and baleen (n = 8) whales, and a combined toothed-baleen group (n = 18): toothed, −161 ± 41 14C yrs (Marine20), 1 ± 41 14C yrs (Marine13); baleen, −158 ± 43 14C yrs (Marine20), 8 ± 41 14C yrs (Marine13); combined baleen-toothed whales, −160 ± 41 14C yrs (Marine20), 4 ± 49 14C yrs (Marine13). Where identification and separation of baleen and toothed whales is impossible the combined ΔRR term may be used. However, we explicitly discourage the application of existing cetacean ΔRR terms to other marine mammals. Our new ΔRR values are applicable for as long as those broad oceanographic conditions (circulation and ventilation) have persisted, i.e., through the Holocene. We recommend using the latest iteration of the marine calibration curve, Marine20, which seems to better capture the time-variant nature of R compared to Marine13. More ΔRL datapoints for both molluscs and cetaceans would improve the accuracy and precision of ΔRR. In the meantime, our new ΔR terms facilitate the calibration of marine 14C dates across the region, paving the way for meaningful and accurate late Quaternary histories and inter-regional comparisons.  相似文献   

15.
Organic carbon in estuarine sediments can have many different sources. Terrestrial, riverine, estuarine and marine C pools may all contribute to and influence the organic C (Corg) inventory of the estuarine sediments and the differing stable isotope signatures of the sources are reflected in the sediment's overall 13C content. Ecological interpretations of sedimentary isotope data may, however, be limited by the fact the total Corg inventory of a sediment may not be an accurate representation of the fraction that is labile and being actively turned over by the sedimentary community. To gain a better understanding of sedimentary Corg dynamics in estuaries and the relationship between the sedimentary C pool and the Corg undergoing mineralisation, we studied three components of an estuarine system: (1) the sedimentary Corg inventory on a transect from the mouth to the upper end of the estuary, (2) temporal changes of sedimentary Corg at one station throughout a year, and (3) the δ13C of respired CO2 compared to the δ13C of available source material and sedimentary Corg in a novel application of methods developed for soil science. Our experiments demonstrated that material of marine origin dominated the studied estuary. At the time-series station, material of marine origin dominated the sedimentary Corg throughout the 1-yr study period. δ13C values of CO2 released from the sediment differed significantly from the sedimentary Corg inventory at all study sites, but also clearly reflected differences between the main sections of the estuary. These results suggest that δ13C measurements of respired CO2 are promising as a tool to advance our understanding of C cycling in estuaries, and highlight that the sedimentary Corg pool alone may not be a satisfactory indicator of OM utilisation in estuarine sediments.  相似文献   

16.
A comprehensive study of a sandy aquifer of deltaic origin in southern Poland included water chemistry, isotopes, dissolved trace gases and transport modelling. Tritium, sulphur hexafluoride (SF6) and freons (F‐11, F‐12 and F‐113) showed the presence of modern waters in the recharge areas and shallow confined parts of the aquifer. The presence of older Holocene waters farther from the recharge areas was indicated by lack of 3H, SF6 contents ≤0·02 fmol l−1 and relatively low 14C values. The discharge from the system is by upward seepage in the valley of a major river. Pre‐Holocene waters of a cooler climate, identified on the basis of δ18O, δ2H, 14C, Ne and Ar data, were found in some distant wells. Concentrations of N2, Ne and Ar determined by gas chromatography were used for calculating the noble gas temperatures, air excess needed for correction of SF6, and nitrogen content released by denitrification process. The time series of 3H content available for some wells supplied quantitative information on age distributions and the total mean ages of flow through the unsaturated and saturated zones. The derived 3H age distributions turned out to be very wide, with mean values in the range of about 30 to 160 years. For each well with determined 3H age, the SF6 data showed either a lower age range or the possibility of a lower age as expected due to shorter travel times of SF6 through the unsaturated zone, which most probably also resulted in different types of age distributions of these tracers. Freons appeared to be of little use for individual age determinations. A quantitative estimation of two‐component mixing from SF63H relations is not possible unless the travel time of 3H through the unsaturated zone is comparable to that of SF6. The ratio of integrals of the response function over the age range with tracer and the whole response function yields the ratio of water with tracer to total flow of water. That ratio is a tracer‐dependent function of time. Transport modelling of SF6 tracer done with MT3D code yielded initially large discrepancies between calculated and measured tracer concentrations. Some discrepancies remained even after calibration of the transport model with SF6. Simulation of tritium contents with a calibrated transport model yielded reasonable agreement with measured contents in some wells and indicated a need for further investigations, particularly in the eastern part of the aquifer. The existence of distinct hydrochemical zones is consistent with the tracer data; young waters with measurable 3H and SF6 contents are aerobic and of HCO3 Ca or HCO3 SO4 Ca types. Slightly elevated Na and Cl contents, as well as the highest concentrations of SO4 and NO3 within this zone are due to anthropogenic influences. Anaerobic conditions prevail in the far field, under the confining cover, where pre‐bomb era Holocene waters dominate. In that zone, dissolved oxygen, NO3 and U contents are reduced, and Fe, Mn and NH4 contents increase. In the third zone, early Holocene and glacial waters occur. They are of HCO3 Ca Na or HCO3 Na types, with TDS values higher than 1 g l−1 and Na content higher than 200 mg l−1, due to either small admixtures of ascending or diffusing older water or freshening of marine sediments, a process that is probably occurring till the present time. Copyright © 2005 John Wiley & Sons, Ltd.  相似文献   

17.
Revealing of the sources and distributions of sedimentary organic matter in the East China Sea (ECS) is important for understanding its carbon cycle, which has significant temporal and spatial variability due to the influences of recent climate changes and anthropogenic activities. In this study, we report the contents of both terrestrial and marine biomarkers including ∑C27+C29+C31n-alkanes (38.6-580 ng/g), C37 alkenones (5.6-124.6 ng/g), brassicasterol (98-913 ng/g) and dinosterol (125-1521 ng/g) from the surface sediments in the Changjiang River Estuary (CRE) and shelf areas of the ECS. Several indices based on biomarker contents and ratios are calculated to assess the spatial distributions of both terrestrial and marine organic matter in the ECS surface sediments, and these results are compared with organic matter distribution patterns revealed by the δ13C (−20.1‰ to −22.7‰) and C/N ratio (5-7.5) of total organic matter. The contents of terrestrial biomarkers in the ECS surface sediments decrease seaward, controlled mostly by Changjiang River (CR) inputs and surface currents; while higher contents of the two marine biomarkers (brassicasterol and dinosterol) occur in upwelling areas outside the CRE and in the Zhejiang-Fujian coastal zone, controlled mostly by marine productivity. Four proxies, fTerr(δ13C) (the fraction of terrestrial organic matter in TOC estimated by TOC δ13C), odd-alkanes (∑C27+C29+C31n-alkanes), 1/Pmar-aq ((C23+C25+C29+C31)/(C23+C25) n-alkanes) and TMBR (terrestrial and marine biomarker ratio) (C27+C29+C31n-alkanes)/((C27+C29+C31) n-alkanes+(brassicasterol+dinosterol+alkenones)), reveal a consistent pattern showing the relative contribution of terrestrial organic matter (TOM) is higher in the CRE and along the Zhejiang-Fujian coastline, controlled mostly by CR inputs and currents, but the TOM contribution decreases seaward, as the influences of the CR discharge decrease.  相似文献   

18.
Radiocarbon dating of Arctic marine sediment is often challenging due to the low availability of calcareous fossils. Consequently, bulk organic matter dating has at times been used to establish sediment core chronologies. Yet, radiocarbon dates based on bulk organic matter often appear to deviate vastly from dates based on fossils, mainly caused by input of allochthounous carbon, including terrigenous organic matter. In this study, we aim to examine the link between the composition of the bulk organic matter and the age offsets between the bulk radiocarbon dates and those obtained from calcareous foraminiferal tests. All samples are taken from the marine sediment core AMD14-204C from offshore Upernavik (eastern Baffin Bay). The radiocarbon dates for bulk organic matter are on average ∼3000 years older than the radiocarbon dates based on foraminifera, but with changing age offsets throughout the record. To investigate the cause of this age offset and its variations over time, we applied core scanning, X-ray Fluorescence analysis, stable isotopes, organic pyrolysis and microscopic organic petrology to examine the distribution and characterization of the organic matter. The results show that the older organic matter includes clastic input of reworked sedimentary rocks potentially originating from West Greenland and/or the Canadian Arctic Archipelago. Changes in the input of contemporary marine algal produced organic matter versus both terrigenous input and reworked ancient organic matter appear to control the age offsets between the bulk and foraminifera dates. A low Hydrogen Index and low δ13Corg values together with a high Oxygen Index, indicative of high influence of terrigenous organic matter, seem to correspond to samples with the largest age offsets; 1000–2000 years greater than in other samples. To examine the cause of the variations in the age offsets, a new quantification of the autochthonous organic matter as a fraction of the TOC was calculated. This shows that samples with the largest age offsets contained the lowest fraction (as low as ∼12%) of autochthonous organic matter in the TOC.  相似文献   

19.
Global marine vessels emissions are adversely affecting human health particularly in southeast Asia. But health burdens from both ocean- and river-going vessels in Pearl River Delta (PRD) regions are not quantified. We estimated the potential health impacts using pooled relative risks of mortality and hospital admissions in China, and the model derived concentrations of sulfur dioxide (SO2), particulate matter (PM10), nitrogen dioxide (NO2) and ozone (O3) due to vessels emissions. SO2 concentrations due to marine emissions in Hong Kong were 13.6 μgm?3 compared with 0.7 μgm?3 in PRD regions that were far from the marine vessels. In PRD regions, the estimated annual numbers (per million people) of excess deaths from all natural causes and hospital admissions from cardiorespiratory causes attributable to SO2, NO2, O3 and PM10 combined from marine emissions were 45 and 265 respectively. Marine emission control measures could contribute a large reduction in mortality and hospital admissions in PRD regions especially in Hong Kong.  相似文献   

20.
The studies of the oxgen and carbon isotopes of the rainwater in Guilin area, the drip water and the present carbonate deposit in Panlong cave of Guilin show that: (i) as to the general characteristics of the oxygen isotopes of the rainwater within a year and between years, the δ18O values decrease with an increase of air temperature and the rainfall, and the correlation between δ18O values and the mean monthly air temperature is much better than that between δ18O values and the rainfall, and the δ18O values of the rainwater during the summer monsoon are much smaller than those during winter monsoon; (ii) δ18O values of the drip water have a quite good correlation with the δ18O values of the rainwater in the same period; (iii) when the conditions are appropriate, δ13C can be used as an environmental proxy, that is, the smaller δ13C of speleothems is, the larger the proportion of C3 plants is and the more plentiful the rainfall is. On the contrary, C4 plants may be prevailing or the environment may be a stony desert caused by climate changes or human activity.  相似文献   

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