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1.
本文对白令海北部陆坡B2-9站位沉积物岩芯开展了高分辨率的生物标志物分析,获得了研究区近一万年来陆源长链正构烷烃（简写为烷烃）的输入及其源区植被结构的变化等相关记录。结果表明,nC27是烷烃中最高的主碳峰,对烷烃总量的贡献也最大,这可能与源区木本植物的丰度及其分布有关;nC23的含量也较高,可能主要是来源于北半球沿海地区广泛分布的一类沉水植物。全新世期间,烷烃总量分别在7.8 ka B.P.,6.7 ka B.P.和5.4 ka B.P.经历了三次阶梯状的下降过程,呈现出四个相对稳定的阶段,可能主要受控于早全新世海平面上升以及源区气候环境和植被分布的变化。烷烃的分子组合特征各参数（如CPI、ACL以及nC31/nC27等）的变化则表明,烷烃主要来自陆生高等植物,且全新世期间植被结构较为稳定,木本植物占据优势。此外,在几个较短的时期内,烷烃总量及其分子组合特征等参数的变化具有同步性,表明在这些时期特殊的气候条件下,源区木本植物烷烃对烷烃总量的贡献率的增加可能低于草本植物烷烃和化石烷烃。  相似文献   

2.
为了解自末次间冰期以来这一地区的古海水表层温度变化,应用气相色谱技术对取自冲绳海槽东侧的Z14?6孔的长链(C37)不饱和烯酮进行了分析。结果发现,该孔Uk37在0.83—0.95之间,其变化趋势与两种浮游有孔虫N.dutertrei和G.sacculifer的氧同位素组成一致。根据Uk37重建的SST在24.0—27.5℃之间变化,最高值27.5℃出现在MIS-5,最低值24℃出现在MIS-2(LGM)。从LGM到全新世SST增加约2℃。这与早期在附近地区根据Uk37重建的SST变化趋势一致。根据重建的SST自LGM以来的变化,作者认为现代黑潮洋流系统最晚在约10kaB.P.后已在冲绳海槽重新建立。许多早期研究揭示的黑潮在7.5—7kaB.P.的加强可能与全新世大暖期有关。  相似文献   

3.
The late glacial to Holocene sedimentary record of the northern shelf of the Sea of Marmara (SoM) has been documented by detailed seismo-, chrono-, and biostratigraphic analyses using sub-bottom (Chirp) profiles and sediment cores. During MIS 3 and the main part of MIS 2 (60–15 14C ka b.p.), disconnection from the Mediterranean and Black seas together with a dry climate resulted in a regression in the SoM, when the Sea was transformed into a brackish lake. The river incisions below 105 m water depth along the northern shelf took place during the last glacial maximum, when the lake level was modulated by stillstands at −98 and −93 m. The post-glacial freshwater transgressive stage of the Marmara ‘Lake’ occurred between 15 and 13.5 14C ka b.p., leading to a rise in water level to −85 m by 13.0 14C ka b.p., as evidenced by broad wave-cut terraces along the northern shelf. Since 12 14C ka b.p., high-frequency sea-level fluctuations have been identified at the SoM entrance to the Strait of İstanbul (SoI). Thus, wave-cut terraces have been recorded at water depths of −76 and −71 m that, according to an age model for core MD04-2750, have ages of 11.5 and 10.5 14C ka b.p., respectively. Ancient shoreline at −65 m along the northern shelf presumably formed soon after the Younger Dryas (YD) at ca. 10.1 14C ka b.p. Moreover, there is compelling evidence of Holocene outflow from the Sea of Marmara to the Black Sea. At the SoM entrance to the SoI, the existence of bioherms on the reflector surface together with abundant Brizalina spathulata and Protoglobulimina pupoides in a core suggests a return to higher salinities due to strong Mediterranean water incursion into the SoM at ∼8.8 14C ka b.p. This finding is consistent with earlier suggestions that, after the YD, the Black Sea was flooded by outflow from the SoM as a result of global sea-level rise.  相似文献   

4.
报道了长江口及邻近海域现代沉积物中正构烷烃的浓度及分布特征,通过因子分析法对正构烷烃来源进行了探讨.结果表明,调查站位正构烷烃主要可归纳为3种类型:陆源输入优势型(单峰群)、陆源和海洋内生混合类型(双峰群)和石油类污染类型(单峰型,不具奇偶优势).长江口邻近站位正构烷烃色谱指标的突变,是长江河口区2种不同水团造成沉积物差异的客观反映.除P4外,研究站位总正构烷烃含量(∑n-Alk)与有机碳总量(TOC)相关性良好,且长江口东南-浙江沿岸软泥区正构烷烃的陆源高等植物组分(TER-Alk)、海洋内生组分(PL-1)、奇偶碳优势指数(CPI)等指标与运移距离呈线形关系.在因子分析显示不同来源的4种正购烷烃中,以陆源烷烃输入比重最大(51.5%),在陆源烷烃中又以东海河流物质贡献最大(49.1%);根据因子负荷差异,推测东海北部沉积有机质可能多数来源于苏北沿岸及老黄河口水下三角洲,冲绳海槽区则可能大部分来源于长江及东海内陆架物质,并探讨了其运移机理.  相似文献   

5.
Twelve surface sediments from the southern Okinawa Trough (OT) and nine surface sediments from a nearby river, the Lanyang River (LR), with high sediment discharge were analyzed for comparison of their aliphatic hydrocarbon distributions. Performing cluster analysis on all hydrocarbon data of LR and OT sediments showed that the two areas had a similarity level of only 0.15, meaning that they were quite dissimilar. The average ratio of terrigenous to aquatic n-alkanes was 0.99 for LR sediments and 9.64 for OT sediments, indicating that the concentrations of n-alkanes in LR and OT sediments were quite different. Furthermore, the mean pristane/phytane ratios for LR and OT sediments were 1.01 and 2.57, respectively; the difference between them was significant (Student's t test, at the 99% significance level). The carbon preference index (CPI) of C25–C33 n-alkanes averaged 3.26 (range 2.16–4.59) for LR sediments and 2.92 (range 2.35–5.24) for OT sediments; no significant difference was found between the two CPI averages (Student's t test, at the 99% confidence level). However, higher plant n-alkanes generally maximized at C29 for LR sediments, but maximized at C31 for all OT sediments, strongly indicating significant differences in the origins of the hydrocarbons in these two areas. All present results appear to suggest that LR sediments are not a major hydrocarbon source for OT sediments. In addition, there was no positive, linear correlation between diploptene (hop-22(29)-ene) and terrestrial higher plant n-alkanes for LR and OT sediments.  相似文献   

6.
Elemental (TOC, TN, C/N) and stable carbon isotopic (δ13C) compositions and n-alkane (nC16–38) concentrations were measured for Spartina alterniflora, a C4 marsh grass, Typha latifolia, a C3 marsh grass, and three sediment cores collected from middle and upper estuarine sites from the Plum Island salt marshes. Our results indicated that the organic matter preserved in the sediments was highly affected by the marsh plants that dominated the sampling sites. δ13C values of organic matter preserved in the upper fresh water site sediment were more negative (−23.0±0.3‰) as affected by the C3 plants than the values of organic matter preserved in the sediments of middle (−18.9±0.8‰) and mud flat sites (−19.4±0.1‰) as influenced mainly by the C4 marsh plants. The distribution of n-alkanes measured in all sediments showed similar patterns as those determined in the marsh grasses S. alterniflora and T. latifolia, and nC21 to nC33 long-chain n-alkanes were the major compounds determined in all sediment samples. The strong odd-to-even carbon numbered n-alkane predominance was found in all three sediments and nC29 was the most abundant homologue in all samples measured. Both δ13C compositions of organic matter and n-alkane distributions in these sediments indicate that the marsh plants could contribute significant amount of organic matter preserved in Plum Island salt marsh sediments. This suggests that salt marshes play an important role in the cycling of nutrients and organic carbon in the estuary and adjacent coastal waters.  相似文献   

7.
Rapid shifts in past climate recorded in polar ice sheets have elicited various explanations relating to either thermohaline circulation changes by ice-rafting or natural greenhouse gas concentrations modulated by climatic conditions in the tropics. To compare the tropical paleoclimate record with the polar record, one must choose sediment cores from highly productive ocean regions. Necessarily, such regions reflect the wind records in the tropics, because high productivity is associated with upwelling driven by winds. Comparing tropical precipitation records with high-latitude records is, however, a more difficult task because sediments recording paleoprecipitation usually have low sedimentation rates, and offer coarser resolution relative to polar ice cores. Here, we present δ 18O data of three planktonic species of Foraminifera (a proxy for precipitation) from such a sediment core, spanning the past 35 ka for the equatorial Indian Ocean, which falls under the southwest monsoon (SWM) realm. Results show that minimum SWM precipitation occurred at the Last Glacial Maximum, with a subsequent increase at Termination IA. During the Holocene, SWM precipitation intensified uniformly up to the core top (∼2.2 ka b.p.), as revealed by generally decreasing δ 18O values. Variations in precipitation are consistent with climate changes recorded in polar ice sheets. Although the different resolutions of the two records preclude a rigorous comparison, abrupt cooling/warming events appear to be accompanied by sudden reduction/enhancement in (SWM) rainfall. Thus, mechanisms with time scales much shorter than a millennium, such as natural greenhouse warming (e.g., CH4 concentration), controlled by emissions from the tropics, could have played a major role in high-latitude climate change.  相似文献   

8.
The Storegga Slide complex is a multi-stage slope failure on the Norwegian continental margin where the most recent major event occurred 8.1 ka b.p. (calendar years before present). Its northern flank contains pockmark features that are commonly inferred to be related to the historical and modern venting of methane-bearing fluids. Three jumbo piston cores (JPC), one from a pockmark and two background cores at variable distances from this site (proximal, 5 km, and distal, 15 km) on the northern flank of the slide (806–1,524 m water depths), were sampled at 10 cm resolution to assess the geologic record of methane venting in the Nyegga pockmark field. Six down-core radiocarbon measurements on mixed planktonic foraminifer species reveal ages of 9.4–16.4 ka b.p. Bathymodiolus mussel shell horizons, indicators of methane-rich environments, have been dated at 15.8–17.6 and ~22 ka b.p. in the pockmark core. Stable isotope analyses on planktonic (Neogloboquadrina pachyderma sinistral) and benthic (Islandiella norcrossi, Melonis barleeanum) Foraminifera reveal δ18O values indicative of a clear glacial/deglacial transition (−1.5‰ shift in planktonic species). Both planktonic and benthic δ13C signatures record multiple excursions, interpreted to reflect the influence of methane in the environment; these δ13C excursions occur in the pockmark core and also in the distal background core. While authigenic calcite formation on the seafloor may play an important role in producing such excursions, these data together suggest the influence of methane seepage within the pockmark field over the past 25 ka, whereby seepage was particularly active between 13 and 15 ka. This is consistent with previously inferred regional increases in porewater pressure associated with glacial loading and higher sedimentation rates, which can cause gas hydrate and slope instability.  相似文献   

9.
We investigated marine and terrestrial environmental changes at the northern Japan margin in the northwestern Pacific during the last 23,000 years by analyzing biomarkers (alkenones, long-chain n-alkanes, long-chain n-fatty acids, and lignin-derived materials) in Core GH02-1030. The U 37K′-derived temperature in the last glacial maximum (LGM) centered at 21 ka was ∼10°C, which was 2°C lower than the core-top temperature (∼12°C). This small temperature drop does not agree with pollen evidence of a large air temperature drop (more than 4°C) in the Tokachi area. This disagreement might be attributed to a bias of U 37K′-derived temperature within 2.5°C by a seasonal shift in alkenone production. The U 37K′-derived temperature was significantly low during the last deglaciation. Because this cooling was significant in the Kuroshio-Oyashio transition zone, the temperature drops are attributable to the southward displacement of the Kuroshio-Oyashio boundary. Abundant lignin-derived materials, long-chain n-alkanes and long-chain n-fatty acids indicate a higher contribution of terrigenous organic matter from 17 to 12 ka. This phenomenon might have resulted from an enhanced coastal erosion of terrestrial soils due to marine transgression and/or an efficient inflow of higher plant debris to river waters from 17 to 12 ka.  相似文献   

10.
Woei-Lih Jeng   《Marine Chemistry》2006,102(3-4):242-251
The n-alkane average chain length (ACL) is the weight-averaged number of carbon atoms of the higher plant C25–C33 n-alkanes. The abundance of individual n-alkanes from higher plant sources generally increases with increasing carbon number in coastal marine sediments around Taiwan, but this trend is reversed for petrogenic hydrocarbons. The ACL would potentially be lowered if petrogenic hydrocarbons were added to sediments containing biogenic hydrocarbons alone. To test this idea, a marine environment off southwestern Taiwan known to contain both biogenic and petrogenic hydrocarbons and two nearby rivers were selected for investigating possible difference in ACL values between their sediments. The average CPI of C25–C33 n-alkanes was 4.08 ± 2.04 (range 1.90–8.96, n = 15) for the river sediments and 1.70 ± 0.16 (range 1.43–1.97, n = 15) for the marine sediments. The ACL of C25–C33 n-alkanes for river sediments ranged from 29.2 to 30.5 (average 29.9 ± 0.4), and for marine sediments from 28.4 to 29.3 (average 28.9 ± 0.3). The ACL difference between marine and river sediments was significant (Student's t test at 99% confidence) although it appeared small. It is suggested that the ACL can be an additional indicator for detection of petrogenic hydrocarbons in coastal marine sediments.  相似文献   

11.
Surface sediment samples from a matrix of fifty-five sites covering virtually the entire Bohai Sea (Bohai), China were analyzed for total organic carbon (TOC), total nitrogen (TN), n-alkanes, unresolved complex mixture (UCM), biomarkers and stable carbon isotopic composition (δ13C), and principal component analysis was performed for source identification of organic matter (OM). The distribution of organic carbon correlated well with sediment grain size with the finest sediments having the highest concentration, suggesting the influence of hydrodynamics on the accumulation of sedimentary organic matter (SOM). The corrected TOC/ON (organic nitrogen) ratios and δ13C indicated mixed marine and terrestrial sources of SOM. Results suggested that δ13C could be used as a potential indicator to observe the dispersion of Huanghe-derived sediments in Bohai. Total n-alkane concentrations varied over 10-fold from 0.39 to 4.94 μg g− 1 (dry weight) with the maximum terrigenous/aquatic alkane ratio observed at the Huanghe River Estuary (HRE) due to more higher plant OM from riverine inputs. C12–C22 n-alkanes with even-to-odd predominance were observed in several central-eastern Bohai sites. The HRE and its adjacent area is the main sink for the Huanghe river-derived OC. The ubiquitous presence of UCM, biomarkers (hopanes and steranes) and PCA results indicated the presence of petroleum contamination in Bohai, mainly from offshore oil exploration, discharge of pollutants from rivers, shipping activities and atmospheric deposition.  相似文献   

12.
Based on new and existing data on oxygen isotopes, alkenone-surface seawater temperature trends, planktonic foraminifers, lithology, and clay mineral composition of piston cores, a distinct cooling event has been identified around 8,200 cal a b.p. in the middle Okinawa Trough, northwest Pacific. This corresponds to the 8,200 a b.p. cooling event recorded in many places of the Northern Hemisphere. During this event, the local temperature decreased by 1°C, and the δ18O value increased by 0.6‰. A strengthened Asian winter monsoon is the most probable cause for this event, which thus adds further credibility to the contention that we are dealing here with a global phenomenon.  相似文献   

13.
The optimum conditions were selected for the chromatographic separation of model mixtures of C12–C40 n-alkanes. For one of the samples of hydrothermal deposits, the extraction conditions of the hydrocarbons were studied and a sample preparation procedure was selected. A procedure is proposed to determine the n-alkanes in samples of hydrothermal deposits by means of gas chromatography-mass spectrometry (GC-MS). The detection limit for the n-alkanes amounted to 3 × 10−9 to 10−8% depending on the components. On the basis of the procedure proposed, the composition of the n-alkanes was studied in the samples of hydrothermal deposits collected at the Mid-Atlantic Ridge (the Broken Spur, Lost City, and Rainbow fields). The analysis performed showed that the samples treated contained C14-C35 n-alkanes. The concentrations of the n-alkanes considered were rather low and varied from 0.002 to 0.038 μg/g. Hypotheses concerning the genesis of the n-alkanes identified were formed.  相似文献   

14.
A study on the bulk distributions and molecular structures of n-alkanes and polycyclic aromatic hydrocarbons (PAH) in organic matter of the sediments from the Bay of Bengal and the Eastern and Central Indian Basins was undertaken. The former two regions represent areas characterised by “normal” sedimentation while the third one mainly represents a region of “active tectonism”. Content of the hydrocarbons in the sediments of “normal” sedimentation ranges between 4.6 and 10.5 μg/g and aromatic hydrocarbons ranges between 0 and 0.38 μg/g. n-Alkanes in the sediments of the northern deep part of the Bay of Bengal consist mostly of long-chain structures (total C25–C33 up to 70%) with a high carbon preference index (CPI=3.01–3.43), indicating a large contribution of organic matter from terrigenous sources. The sediments from the Eastern Indian Basin have n-alkane distributions in which the long-chain components did not exceed 52.5% and the CPI was 1.7–1.90, indicating that the hydrocarbons are mostly derived from marine sources. Sharp increases of hydrocarbons are found in the vicinity of the tectonically active region of the Central Indian Basin, particularly in the sediments collected from the fracture zone. The total concentration of hydrocarbons increase to 170 μg/g and the aromatic hydrocarbons fraction to 156.3 μg/g. The proportion of short-chain n-alkanes increases up to 70%, CPI decreases to 0.76–1.12, and high concentrations of n-C16 (16–40%) occur, all of which are absent in the other samples. The molecular content of PAH includes the unsubstituted individual structures: biphenyl, fluorene, pyrene, perylene, benzo(ghi)perylene, and the groups of homologues of naphthalene, benzofluorene, phenanthrene and chrysene. The association of the PAH and composition of paraffin hydrocarbons in the surficial sediments of deformation zone indicate that these are the resultant products of hydrothermal processes. It is, therefore, suggested that the association and composition of the hydrocarbons in sediments can be utilised as a paleoceanographic parameter to decipher the history of tectonism of an area.  相似文献   

15.
The sedimentation rates in the Okinawa Trough during the Late Quaternary   总被引：3，自引：0，他引：3  
On the basis of accelerator mass spectrometer radiocarbon （AMS ^14C） dating, sedimentation rates of 11 cores collected from the northern to southern Okinawa Trough are discussed. The sedimentation rates in the Okinawa Trough roughly range from 11 to 39cm/ka, and the average is 23.0cm/ka. China＇s continental matter is the main sediment source of the middle Okinawa Trough and has important contribution to the northern and southern Okinawa Trough. The sedimentation rates during the marine oxygen isotope （MIS） 2 are uniformly higher than those during MIS 1 in the northern and middle Okinawa Trough while they are on the contrary in the southern Okinawa Trough. Sedimentation rates in the Okinawa Trough can be one of the proxies of sediment source and an indicator of cooling events.  相似文献   

16.
《Marine Geology》1999,153(1-4):303-318
Organic geochemistry and micropaleontology are used to determine the origin of sapropel S1 in the Aegean Sea. Low-molecular-weight (C15, C17 and C19) n-alkane data show that net primary productivity (NPP) increased from ∼14,000 to 10,000 yr BP at the glacial interglacial transition, but the onset of S1 at 9600 yr BP marks a sharp decline in NPP, which remained low until ∼8200 yr BP. The start of sapropel deposition is marked by increased total organic carbon (TOC) and pollen-spore concentrations, together with increased high-molecular-weight (C27, C29, C31 and C33) n-alkanes. Pollen assemblages show large influx of tree pollen from central-northern European forests. Increases in high-molecular-weight n-alkanes suggest greater influx of fresh vascular plant material at the start of S1, although the amount is small compared to other insoluble organic matter. Palynological studies showed that most of this insoluble organic matter are flocks of dark-brown amorphous kerogen, typical of terrigenous humic compounds. From ∼8200 yr BP to the top of S1 at ∼6400 yr BP, there is a decline in high-molecular-weight n-alkanes and terrigenous kerogen, and an increase in low-molecular-weight n-alkanes, suggesting that NPP recovered during the later deposition of S1 in the Aegean Sea. The increase in low-molecular-weight n-alkanes coincides with the recovery of coccolithophores and dinoflagellates, suggesting that these phytoplankton are primarily responsible for the low-molecular-weight n-alkane variations. These data from the Aegean Sea support the model for sapropel deposition resulting from increased influx of TOC during times of stagnant bottom water, but disagree with Mediterranean models prescribing a large increase in marine productivity.  相似文献   

17.
To examine the source and preservation of organic matter in the shelf sediments of the East China Sea (ECS), we measured bulk C/N and isotopes, organic biomarkers (n-alkanes and fatty acids) and compound-specific (fatty acids) stable carbon isotope ratios in three sediment cores collected from two sites near the Changjiang Estuary and one in the ECS shelf. Contrasting chemical and isotopic compositions of organic matter were observed between the estuarine and shelf sediments. The concentrations of total n-alkanes and fatty acids in the shelf surface sediments (0–2 cm) were 5–10 times higher than those in estuarine surface sediments but they all decreased rapidly to comparable levels below the surface layer. The compositions of n-alkanes in the estuarine sediments were dominated by C26-C33 long-chain n-alkanes with a strong odd-to-even carbon number predominance. In contrast, the composition of n-alkanes in the shelf sediment was dominated by nC15 to nC22 compounds. Long-chain (>C20) fatty acids (terrestrial biomarkers) accounted for a significantly higher fraction in the estuarine sediments compared to that in the shelf sediment, while short-chain (<C20) saturated and unsaturated fatty acids were more abundant in the shelf surface sediments than in the estuarine sediments. Stable carbon isotopic ratios of individual fatty acids showed a general positive shift from estuarine to shelf sediments, consistent with the variations in bulk δ 13CTOCTOC. These contrasts between the estuarine and shelf sediments indicate that terrestrial organic matter was mainly deposited within the Changjiang Estuary and inner shelf of ECS. Post-depositional diagenetic processes in the surface sediments rapidly altered the chemical compositions and control the preservation of organic matter in the region.  相似文献   

18.
Organic matter in eolian dusts over the Atlantic Ocean   总被引：1，自引：0，他引：1  
The elemental and mineralogical composition and the microfossil and detritus content of particulate fallout from the lower troposphere over the Atlantic Ocean have been extensively documented in earlier work, and it was possible to ascribe terrigenous source areas to such fallout. A brief review of the organic geochemistry of eolian dust is also presented here. The lipids of eolian dusts sampled from the air mass over the eastern Atlantic from about 35°N to 30°S were analyzed here.These lipids consisted mainly of normal alkanes, carboxylic acids and alcohols. The n-alkanes were found to range from n-C23 to n-C35, with high CPI values and maximizing at n-C27 in the North Atlantic, at n-C29 in the equatorial Atlantic and at n-C31 in the South Atlantic. The n-fatty acids had mostly bimodal distributions, ranging from n-C12 to n-C30 (high CPI), with maxima at n-C16 and in the northern samples at n-C24 and in the southern samples at n-C26. The n-alcohols ranged from n-C12 to n-C32, with high CPI values and maxima mainly at n-C28. The compositions of these lipids indicated that their terrigenous sources were comprised mainly of higher plant vegetation and desiccated lacustrine mud flats on the African continent.  相似文献   

19.
The spatial distributions of δ13C, δ15N, and n-alkanes were investigated to determine the source and transportation of allochthonous organic matter from the mouth of the Seomjin River to the southern inner shelf break of Korea. Total organic carbon (%) ranged from 0.3% to 1.6% (average = 0.80%, n = 81), and the C/N ratio varied from 2.4 to 12.4 (average = 6.76, n = 81). The δ13C values ranged from ?25.86 to ?20.26‰ (average = ?21.47‰, n = 81), and δ15N values ranged from 4.37‰ to 8.57‰ (average = 6.72‰, n = 81). The contribution of the terrestrial fraction of organic matter to the total ranged from 4.4% to 97.7% (average = 24.4%, n = 81), suggesting higher amounts around the catchment area and lower amounts in the offshore area. The concentration of total n-alkanes (nC25 ? nC35) was higher at the boundary between the outer bay and inner shelf break (BOBIS). Average chain length and the carbon preference index both indicated that major leaf wax n-alkanes accounted for the observed distribution of terrestrial organic matter, and were dominant in the inner shelf break (around BOBIS) and outer shelf break. Based on the spatial distribution of the total n-alkanes and the sum of nC27, nC29, and nC31, the terrestrial organic matter distribution was considered to be controlled by local oceanographic conditions, especially at the center of the BOBIS. In addition to enabling the distribution and source of terrestrial organic matter to be identified, the n-alkanes indicated that minor anthropogenic allochthonous organic materials were superimposed on the total organic materials in the central part of Yeosu Bay and the catchment area. The n-alkane indices revealed weathered petroleum contamination, with contamination levels being relatively low at the present time.  相似文献   

20.
Within the framework of the European project EROS 21, a biogeochemical study of particles transported from the Danube Delta to the Northwestern Black Sea whose carbon cycle is dominated by riverine inputs was carried out in spring off the Sulina branch of the Danube Delta. The distribution of particulate organic carbon (POC), chlorophyll a (Chl a), C/N, and δ13C evidenced an omnipresent contribution of terrestrial organic matter throughout the study area together with a dilution of these inputs by freshwater and marine organisms. Four lipid series, n-alkanoic acids, n-alkanes, n-alkanols, and sterols were analyzed by gas chromatography and gas chromatography/mass spectrometry. Several signature compounds were selected to delineate dispersion of terrestrial organic carbon: (1) long-chain n-alkanoic acids in the range C24–C34, long-chain n-alkanes in the range C25–C35, long-chain n-alkanols in the range C22–C30, 24-ethylcholesta-5,22-dien-3β-ol (29Δ5,22) and 24-ethylcholesterol (29Δ5) for vascular plant-derived material and (2) coprostanol (27Δ0,5β) for faecal contamination associated with sewage effluents. A marked decrease was observed between the concentrations of different vascular plant markers characterizing the two end members: riverine at salinity 0.3 and marine at salinity 15.5. The decrease observed for marine/riverine end members (expressed as a function of organic carbon) varied in a large range, from 4% for n-alkanes to 18.6%, 20.4% and 24% for n-fatty acids, n-alkanols and sterols, respectively. These values reflect a combination of various processes: size-selective particle sedimentation, resuspension of different particle pools of different sizes and ages, and/or selective biological utilization. The multi-marker approach also suggested the liberation in the mixing zone of terrestrial moieties, tightly trapped in macromolecular structures of the riverine material. The greatest decrease for marine/riverine end members was observed for coprostanol (0.9%), underlining the efficiency of the mixing zone as a sink for sewage-derived carbon.  相似文献   

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