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东海季节性低氧海区柱状沉积物中氧化还原敏感元素对沉积环境变化的响应 总被引：3，自引：1，他引：2
氧化还原敏感元素(Redox Sensitive Elements，RSE)如V、Cr、Mo、U等，通常在氧化条件下呈溶解态，在还原沉积环境中除Fe、Mn外，RSE被还原成低价态转移至沉积物中富集积累，因此可以利用氧化还原敏感元素在沉积物中的富集情况反演沉积环境的氧化还原状况。本文通过研究东海内陆架季节性低氧海区Zb7沉积柱中氧化还原敏感元素V、Cr、Ni、Cu、Zn、Mo、U的垂直分布、富集特征和比值，探究沉积环境氧化还原状况；发现RSE/Al和富集系数自1978年以来呈增加的趋势，但自2009年开始有所降低，整体RSE富集系数均小于3，未见明显富集。RSE比值V/Cr<2、Ni/Co<5、U/Th<0.75、0.25<(Cu+Mo)/Zn<0.55，以及MoEF/UEF比值主要分布在0.08～0.3倍海水Mo/U值之间，均指示氧化的沉积环境。RSE/Al与Fe/Al、Mn/Al具有显著的相关性，表明RSE在剔除陆源碎屑输入后，主要通过与Fe、Mn氧化物结合进入沉积物，也指示氧化的沉积环境。研究结果与该区域溶解氧历史数据反映的季节性低氧结果不一致，可能与RSE在夏季季节性低氧时，沉积物中的富集信号在秋冬季溶氧水平恢复后缺失有关。尽管RSE不能有效指示东海季节性低氧环境，但Zb7沉积柱RSE在1978年后富集程度的增加以及2011年后的降低，在一定程度上反映了该区域自1978年后季节性低氧程度加重，2009年后又有所缓解的变化趋势。 相似文献
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Two sediment cores, ABP-32/GC-01R and ABP-32/GC-03 were collected at a water depth of 642 m and 1086 m off Goa from the present day Oxygen Minimum Zone (OMZ) of eastern Arabian Sea (EAS) cover time span of last 18 ka and 32 ka respectively were analysed for multi-proxy redox-sensitive elements to understand the variation in the redox conditions and factors responsible for its development.Redox-sensitive elements concentration and their normalized ratios (Mn/Al, U/Th, Mo/Al and Ce/Ce*) suggest that sediment core ABP-32/GC-01R is under more reducing conditions due to its location within the centre of OMZ compared to core ABP-32/GC-03 which is at the base of OMZ. Sediments from the EAS are of non-euxinic environments where dissolved sulfide is present but restricted to the sediment pore-waters. Lack of significant correlation (r=< 0.1) of organic carbon with U and Mo suggest that productivity may not have control on the development of reducing conditions. The lowest Mn/Al ratio, strong negative Ce/Ce* anomaly and remarkable enrichment of U/Th and Mo/Al ratios during the last deglaciation, and Heinrich events (H1, H2, H3) indicate intense reducing conditions probably due to poor ventilation by oxygen depleted bottom waters from Subantarctic Mode Waters (SAMW) - Antarctic Intermediate waters (AAIW). There is a distinct lathanide fractionation in the sediment cores where, La(n)/Yb(n) ratio is <1, ≈1 and >1 during the last 10 ka (Holocene), 14–10 ka (includes-Younger Dryas and Bǿlling-Allerǿd), 18–14 ka (last deglaciation) and Heinrich events suggesting less reducing, terrigenous dominated and intense reducing condition respectively. 相似文献
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Authigenic barite nodules associated with modestly 13C-depleted calcium carbonate concretions and 34S-enriched pyrite at the bottom of the Upper Devonian Hanover Shale of western New York provide evidence of sulfate reduction coupled with anaerobic oxidation of methane (AOM). The methane, much of it biogenic in origin, may have diffused upward from Middle Devonian Marcellus Shale and perhaps the Upper Ordovician Utica Shale. Strong 34S enrichment and high δ34S/δ18O values of the barite nodules reflect: (1) substantial kinetic fractionation induced by microbial sulfate reduction perhaps intensified by a low seawater sulfate recharge rate and (2) upward delivery of Ba2+- and CH4- bearing pore fluid sourced within underlying sulfate-depleted deposits. However, the association of authigenic calcium carbonate and barite in the same stratigraphic interval, especially the presence of barite overgrowths on carbonate concretions, is not consistent with what is known of AOM-related mineralization of a sediment column passing downward through the sulfate–methane transition (SMT). The documented early formation of authigenic carbonate followed by barite observed relations may reflect a diminished rate of methanogenesis and/or CH4 supply. The tempered methane flux would have induced the SMT to descend the sediment column enabling barite to form within the same stratigraphic horizon that 13C-depleted calcium carbonate had most recently precipitated. Diminished methane flux may have been caused by burial-related passage of the organic-rich Marcellus Shale below the depth of peak biogenic methane generation and its replacement at that depth interval by organic-lean deposits of the upper part of the Hamilton Group. Subsidence of the SMT would have increased the preservation potential of authigenic barite. However, continued survival of the labile barite as it eventually moved through the SMT suggests that the underlying sulfate-depleted zone was strongly enriched in Ba2+. 相似文献
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The trace and rare earth elements (REE) analyses were conducted on samples collected from a 30 m core of the Marcellus Shale obtained from Greene County, southwestern Pennsylvania. Our results suggest that organic matter enrichment trends in the Marcellus Shale can be directly linked with the Acadian Orogeny. The Acadian Orogeny has been recognized as a main sediment source for the Marcellus Shale. Synthesis of tectonic history and recent ash bed geochronology, reveals that deposition of the organic carbon-rich (OR) zone (characterized by TOC >4%; located between 2393 m and 2406.5 m core depth) in the studied Marcellus Shale core was coincident with tectonically active and magmatic quiescent period of the Acadian orogeny (ca. 395–380 Ma). This time period also corresponds to the highest rate of mountain building in the Acadian Orogeny. The light rare earth (LREE) and selected trace elemental (e.g., Ta, Cs) composition of the OR zone sediments is similar to that of the bulk continental crust, supporting the lack of magmatic activity in the source area (i.e. Acadian Orogeny). In contrast, subsequent deposition of the organic carbon-poor (OP) sediments (characterized by TOC <4%; located between 2376 m and 2393 m core depth) in the upper Marcellus Shale occurred synchronously with a magmatic active phase (ca. 380–370 Ma) during the Acadian orogeny. The OP zone sediments have LREE and trace elemental composition similar to the average of the upper continental crust, suggesting intrusion of granodiorite rocks during a magmatic active period of Acadian Orogeny. The temporal and geochemical correlation between the Acadian orogenesis and the Marcellus deposition provide evidence for the role of tectonism in the enrichment of organic matter in the Marcellus Shale. 相似文献
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The Middle Triassic Botneheia Formation of eastern Svalbard (Edgeøya and Barentsøya) comprises an organic carbon-rich, fine-grained clastic succession (∼100 m thick) that makes the best petroleum source rock horizon in the NW Barents Sea shelf. The succession records a transgressive–regressive interplay between the prodelta depositional system sourced in the southern Barents Sea shelf (black shale facies of the lower and middle parts of the Muen Member) and the open shelf phosphogenic system related to upwelling and nutrient supply from the Panthalassic Ocean (phosphogenic black shale facies of the upper part of the Muen Member and the Blanknuten Member). The relationships between organic matter, authigenic apatite, and pyrite in these facies allow to characterize the relative roles of redox conditions and oceanic productivity in the organic carbon preservation. The accumulation of terrestrial and autochthonous marine organic matter in the black shale facies occurred under dominating oxic conditions and increasing-upward productivity related to early transgressive phase and retrogradation of the prodelta system. The phosphogenic black shale facies deposited in an oxygen-minimum zone (OMZ) of the open shelf environment during the late transgressive to regressive phases under conditions of high biological productivity, suppressed sedimentation rates, and changing bottom redox. The phosphatic black shales occurring in the lower and upper parts of the phosphogenic succession reveal depositional conditions indicative of the shallower part of OMZ, including high input of autochthonous organic matter into sediment, oxic-to-dysoxic (episodically suboxic and/or anoxic) conditions, intense phosphogenesis, and recurrent reworking of the seabed. The massive phosphatic mudstone occurring in the middle of the phosphogenic succession reflects the development of euxinia in the deeper part of OMZ during high-stand of the sea. High input of autochthonous organic matter in this environment was coupled with mineral starvation and intermittent phosphogenesis. In mature sections in eastern Svalbard, the petroleum potential of the Botneheia Formation rises from moderate to good in the black shale facies, and from good to very good in the phosphogenic black shale facies, attaining maximum in the massive phosphatic mudstone. 相似文献
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《Deep Sea Research Part II: Topical Studies in Oceanography》2009,56(16):1124-1135
We study fish scales as a proxy of fish abundance and preservation biases together with phosphorus from fish remains (Pfish) in a sediment core retrieved off Callao, Peru (12°1′S, 77°42′W; water depth=179 m; core length=52 cm). We interpret our results as a function of changing redox conditions based on ratios of redox-sensitive trace elements (Cu/Al, Mo/Al, Ni/Al, Zn/Al, V/Al), terrigenous indicators (Fe in clays, Ti, Al), and biogenic proxies (CaCO3, biogenic opal, total nitrogen, organic carbon, barite Ba). The core covers roughly 700 years of deposition, based on 210Pb activities extrapolated downcore and 14C dating at selected intervals. Our fish-scale record is dominated by anchovy (Engraulis ringens) scales followed by hake (Merluccius gayii) scales.The core presented an abrupt lithological change at 17 cm (corresponding to the early 19th century). Above that depth, it was laminated and was more organic-rich (10–15% organic carbon) than below, where the core was partly laminated and less organic-rich (<10%). The lithological shift coincides with abrupt changes in dry bulk density and in the contents of terrigenous and redox-sensitive trace elements, biogenic proxies, and fish scales. The remarkable increase in redox-sensitive trace elements in the upper 17 cm of the core suggests more reducing conditions when compared with deeper and older horizons, and is interpreted as an intensification of the oxygen minimum zone off Peru beginning in the early 19th century. Higher fish-scale contents and higher Pfish/Ptotal ratios were also observed within the upper 17 cm of the core. The behavior of biogenic proxies and redox-sensitive trace elements was similar; more reduced conditions corresponded to higher contents of CaCO3, Corg, total nitrogen and fish scales, suggesting that these proxies might convey an important preservation signal. 相似文献
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Sedimentary record of redox-sensitive elements (U, Mn, Mo) in a transitory anoxic basin (the Thau lagoon, France) 总被引：4，自引：0，他引：4
Franoise Elbaz-Poulichet Jean Luc Seidel Didier Jzquel Edouard Metzger Franois Prvot Caroline Simonucci Grard Sarazin Eric Viollier Henri Etcheber Jean-Marie Jouanneau Olivier Weber Olivier Radakovitch 《Marine Chemistry》2005,95(3-4):271-281
In order to further document the relation between redox conditions and the sedimentary record of Mn, U and Mo in a transitory anoxic water basin, their distribution has been studied along two profiles in the Thau lagoon (France). Sediments and pore-water have been sampled at two contrasting sites located, respectively, in the shellfish-farming area and in the centre of the lagoon. In the shellfish-farming area, the particulate organic carbon (POC) data indicate a more rapid organic matter mineralisation compared to the centre of the lagoon. This results in a sharper redox gradient characterized by the appearance of H2S in pore-water a few millimetres below the sediment–water interface. In the centre of the lagoon, H2S appears at a depth of 35 cm.In both cores, sedimentary Mn is relatively depleted through out the whole sedimentary column and varies with the proportion of clay minerals. After an initial release into solution at the sediment–water interface in relation to Mn-oxide reductive dissolution, authigenic U is immobilized when sulphides appear. Despite the occurrence of anoxic conditions at the sediment–water interface at the site influenced by shellfish farming, the burial of U is reduced by bioturbation, which raises reducing sediments to the surface. In the centre of the lagoon, Mo profiles reflect continuous diffusion into pore water and immobilization at 15 cm probably in anoxic microenvironments. At shellfish farms, dissolved Mo undergoes removal with sulphides but contrary to U, sedimentary Mo does not appear to be strongly affected by bioturbation. The profile indicates an increase in the frequency of anoxia crises during the second half of the 20th century. 相似文献
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A. Sifeddine D. Gutirrez L. Ortlieb H. Boucher F. Velazco D. Field G. Vargas M. Boussafir R. Salvatteci V. Ferreira M. García J. Valds S. Caquineau M. Mandeng Yogo F. Cetin J. Solis P. Soler T. Baumgartner 《Progress in Oceanography》2008,79(2-4):190
Sedimentological studies including X-ray digital analyses, mineralogy, inorganic contents, and organic geochemistry on cores of laminated sediments accumulated in the oxygen minimum zone of the central Peruvian margin reveal variable oceanographic and climate conditions during the last 500 yr. Coherent upcore variations in sedimentological and geochemical markers in box cores taken off Pisco (B0405-6) and Callao (B0405-13) indicate that variability in the climate proxies examined has regional significance. Most noteworthy is a large shift in proxies at 1820 AD, as determined by 210Pb and 14C radiometric dating. This shift is characterized by an increase in total organic carbon (TOC) in parallel with an abrupt increase in the enrichment factor for molybdenum Mo indicating a regional intensification of redox conditions, at least at the sediment water interface. In addition there was lower terrestrial input of quartz, feldspar and clays to the margin. Based on these results, we interpret that during several centuries prior to 1820, which corresponds to the little ice age (LIA), the northern Humboldt current region was less productive and experienced higher terrestrial input related to more humid conditions on the continent. These conditions were probably caused by a southward displacement of the inter-tropical convergence zone and the subtropical high pressure cell during the LIA. Since 1870, increases in TOC and terrigenous mineral fluxes suggest an increase of wind-driven upwelling and higher productivity. These conditions continued to intensify during the late 20th century, as shown by instrumental records of wind forcing. 相似文献
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南沙海槽表层沉积自生石膏-黄铁矿组合的成因及其对天然气渗漏的指示意义 总被引：9，自引：0，他引：9
南海海槽是潜在的天然气水合物发育区，在表层沉积物中分布有石膏-黄铁矿组合。通过对石膏、黄铁矿的形貌特征、矿物组成、化学元素、硫同位素等的分析，讨论和揭示了石膏-黄铁矿组合的成岩环境、形成机理及其与天然气渗漏的关系。石膏集合体为土块状和多孔状、玫瑰状，表面分布有孔洞或微孔，黄铁矿为莓球状、球粒结块状和虫管状。不同形状的石膏、黄铁矿的化学成分没有明显差别。石膏-黄铁矿的形成机理是海底渗漏的天然气与硫酸盐发生缺氧甲烷氧化反应，产物HS^-与沉积物中的Fe^2＋反应产生FeS并转变为黄铁矿，在形成FeS的过程中产生的H^＋促进碳酸盐溶解，Ca^2＋与SO4^2-达到过饱和沉淀出重。^34S的石膏。因此，石膏-黄铁矿组合是海底存在天然气渗漏的证据，这一发现对开展南沙海槽潜在天然气水舍物的调查以及对天然气渗漏事件的研究具有一定的科学意义。 相似文献
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南海东北部晚更新世以来沉积环境演变的矿物-地球化学记录 总被引：5，自引：6，他引：5
对南海东北部69柱(20°07.10'N,118°49.0'E)沉积物岩心进行碎屑矿物-地球化学特征研究,结果表明,以孔深165cm为界可划分出晚更新世末次冰期沉积和全新世冰后期沉积,这一地层划分结果与根据浮游有孔虫氧、碳同位素分析得出的结果是一致的.末次冰期时自生黄铁矿和硫元素高度富集,钠与铝、镁与铝和钠与钾的比值均较高,重矿物和SiO2含量较高,CaCO3含量较低,反映当时是一种相对闭塞的缺氧环境,气候干寒,化学风化作用较弱,以机械风化作用为主;研究区主要接受粒径较粗的硅质沉积;陆源物质的稀释作用可能是造成碳酸盐含量相对较低的主要原因.冰后期褐铁矿出现高含量,钠与铝、镁与铝和钠与钾的比值均降低,Al2O3和CaCO3含量增高,反映沉积环境渐变为开放的氧化环境,气候转变为化学风化作用较强的湿热气候;研究区以接受较细粒的铝硅酸盐沉积为主,冰消期时还出现了碳酸盐保存高峰事件. 相似文献
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Paola Ridge, along the NW Calabrian margin (southern Tyrrhenian Sea), is one of the few reported deep sea sites of precipitation of authigenic carbonates in the Tyrrhenian Sea. Here, the changing composition of the seeping fluids and the dynamic nature of the seepage induced the precipitation of pyrite, siderite and other carbonate phases. The occurrence of this array of authigenic precipitates is thought to be related to fluctuation of the sulfate-methane transition zone (SMTZ).Concretions of authigenic minerals formed in the near sub-bottom sediments of the Paola Ridge were investigated for their geochemical and isotopic composition. These concretions were collected in an area characterized by the presence of two alleged mud volcanoes and three mud diapirs. The mud diapirs are dotted by pockmarks and dissected by normal faults, and are known for having been a site of fluid seepage for at least the past 40 kyrs. Present-day venting activity occurs alongside the two alleged mud volcanoes and is dominated by CO2-rich discharging fluids. This discover led us to question the hypothesis of the mud volcanoes and investigate the origin of the fluids in each different domed structure of the study area.In this study, we used stable isotopes (carbon and oxygen) of carbonates coupled with rare earth element (REE) composition of different carbonate and non-carbonate phases for tracing fluid composition and early diagenesis of authigenic precipitates. The analyses on authigenic precipitates were coupled with chemical investigation of venting gas and sea-water.Authigenic calcite/aragonite concretions, from surficial sediments on diapiric structures, have depleted 13C isotopic composition and slightly positive δ18O values. By contrast, siderite concretions, generally found within the first 6 m of sediments on the alleged mud volcanoes, yielded positive δ13C and δ18O values. The siderite REE pattern shows consistent LREE (light REE) fractionation, MREE (medium REE) enrichment and positive Gd and La anomalies. As shown by the REE distribution, the 13C-depleted composition and their association with chemosymbiotic fauna, calcite/aragonite precipitated at time of moderate to high methane flux close to the seafloor, under the influence of bottom seawater. Authigenic siderite, on the other hand, formed in the subseafloor, during periods of lower gas discharges under prolonged anoxic conditions within sediments in equilibrium with 13C-rich dissolved inorganic carbon (DIC) and 18O-rich water, likely related to methanogenesis and intermittent venting of deep-sourced CO2. 相似文献
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《Deep Sea Research Part I: Oceanographic Research Papers》1999,46(5):733-755
We analyzed the REE, Mn and Al concentrations and Nd isotopic ratios in marine suspensions collected on filters (0.65 μm porosity) with in situ pumping systems in the tropical northeastern Atlantic (20°N, 18–31°W). Previously we reported the same parameters on large sinking particles collected with moored sediment traps at the sites. Shale-normalized REE patterns of the filtered suspensions are characterized by a larger light REE (LREE) to heavy REE (HREE) enrichment compared to the trapped material and a Ce anomaly that evolves positively with depth. Depth profiles of REE/Al show maximum values at 50–100 m, where the Mn/Al ratio also reaches a maximum. The profile of the Nd isotopic ratios of the filtered suspensions shows variations similar to those of the seawater. These results suggest that the filtered suspensions preferentially scavenge the LREE, especially Ce, and that the particulate Mn oxides are potential REE carriers. The relationship between the Ce anomaly and the Ce/Al ratio demonstrates that the particulate Ce anomaly is formed by (1) the LREE adsorption onto the particulate Mn oxides in the surface water, (2) Ce(III) oxidation to insoluble Ce(IV)O2 and (3) preferential desorption of strict trivalent REE from the Mn oxides in deep water. Estimated authigenic Nd contents, using Nd isotopic ratios, decrease with depth. This is consistent with the adsorption of the REE in surface water and their desorption in deep water, suggested by the Ce anomaly formation. All the results show that the suspended particles record more clearly the authigenic REE contribution than the trapped material does. The suspended matter plays a key role in the scavenging of particle-reactive elements. 相似文献
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The early diagenesis of trace elements (V, Cr, Co, Cu, Zn, As, Cd, Ba, U) in anoxic sediments of the Achterwasser, a shallow lagoon in the non-tidal Oder estuary in the Baltic Sea, was investigated in the context of pyrite formation. The dissolved major redox parameters show a two-tier distribution with transient signals in the occasionally re-suspended fluid mud layer (FM) and a permanently established diagenetic sequence in the sediment below. Intense microbial respiration leads to rapid depletion of O2 within the uppermost mm of the FM. The reduction zones of Mn, Fe and sulfate overlap in the FM and in the permanently anoxic sediment section which appears to be a typical feature of estuarine sediments, under low-sulfate conditions. Degrees of pyritization (DOP) range from 50% in the FM to remarkably high values > 90% at 50 cm depth. Pyrite formation at the sediment surface is attributed to the reaction of Fe-monosulfides with intermediate sulfur species via the polysulfide pathway. By contrast, intense pyritization in the permanently anoxic sediment below is attributed to mineral growth via adsorption of aqueous Fe-sulfide complexes onto pyrite crystals which had originally formed in the surface layer.The studied trace elements show differential behavior patterns which are closely coupled to the diagenetic processes described above: (i) Zn, Cu and Cd are liberated from organic matter in the thin oxic layer of the sediment and diffuse both upwards across the sediment/water boundary and downwards to be trapped as monosulfides, (ii) V, Cr, Co and As are released during reductive dissolution of Mn- and Fe-oxyhydroxides, (iii) U removal from pore water occurs concomitantly to Fe reduction in the FM and is attributed to reduction of U(VI) to U(IV), (iv) the Ba distribution is controlled by reductive dissolution of authigenic barite in the sulfate reduction zone coupled with upward diffusion and re-precipitation. The incorporation of trace elements into pyrite is most intense for Co, Mn and As, intermediate for Cu and Cr and little to negligible for U, Zn, Cd, V and Ba. The observed trend is largely in agreement with previous studies and may be explained with differing rates for ligand exchange. Slow and fast ligand exchange and thus precipitation kinetics are also displayed by downcore increasing (Mn, Cr, Co and As) or constantly low (Zn, Cu, Cd) pore water concentrations. The downward increasing degrees of trace metal pyritization (DTMP) for Co, Cu, Zn and As are, in analogy to pyrite growth, assigned to adsorption of sulfide complexes or As oxyanions onto preexisting pyrite minerals. 相似文献
16.
The concentrations of dissolved aluminum (Al) in the upper St. Lawrence Estuary were determined during periods of high and intermediate river-discharge. Laboratory experiments simulating estuarine processes were also conducted in order to examine possible mechanisms controlling the Al distribution. During the high river-discharge, the Al concentration at river end-member was 1.63 µM and decreased exponentially with increasing salinity. An almost complete removal of dissolved Al was observed in the low salinity area up to 10 with an intensive removal in the turbidity maximum zone. Principal mechanisms responsible for the Al removal inferred from the laboratory experiments were flocculation and adsorption onto suspended particulate matter (SPM). During the intermediate river-discharge, the Al concentration was 0.72 µM at the river end-member and again decreased with increasing salinity. However, the removal was less pronounced, being only about 25%. Good fits with model predictions and laboratory experiments suggest that principal removal mechanisms were authigenic aluminosilicate formation and adsorption onto SPM. In the upper St. Lawrence Estuary, Al distribution is controlled by a combination of three removal mechanisms: flocculation, authigenic aluminosilicate formation, and adsorption. Each mechanism can become a dominant factor depending on the concentration level and speciation of dissolved Al in the river water. 相似文献
17.
The variations in CaCO3 and organic carbon and their inter-relationship in a core from the southeastern Arabian Sea (water depth 2,212 m) have been
used to demarcate the Holocene/Pleistocene boundary; an increased terrigenous deposition during Late Pleistocene has been
inferred. The higher contents of organic carbon and sulfide sulfur and their negative relationship clearly establish the existence
of a reducing environment below 65 cm subbottom depth. The occurrence of pyrite framboids and crystals, present only on the
surface of fecal pellets (80–85 cm), has been discussed in terms of significance of reducing microenvironment. 相似文献
18.
对南海北部陆坡柱状沉积物样品总有机碳、总硫含量,以及其中的自生黄铁矿形貌、含量进行分析．结果显示,沉积物中黄铁矿（FeS2）、总有机碳（TOC）、总硫（TS）的质量分数分别为0～0,71％、0．37％～1．18％、0．04％～0．81％;黄铁矿和总有机碳、总硫的含量随深度加深逐渐增大,达到峰值后不断减少,三者的分布趋势基本一致;扫描电镜下观察到黄铁矿主要以莓球状集合体和八面体微晶形貌产出,局部层位亦发现管状、生物内膜状和立方体状黄铁矿晶体．表明该区浅表层环境为缺氧环境,硫化物主要以黄铁矿形式产出,其成因与有机质的厌氧氧化作用有关,而甲烷的厌氧氧化作用也可能促使自生黄铁矿的加速形成．莓球状黄铁矿占主导亦指示一种强还原性的缺氧微环境．黄铁矿富集的缺氧环境与下伏地层中天然气水合物分解释放的甲烷有关,为天然气水合物在该区的勘探提供一定的科荤依据． 相似文献
19.
Two genetically different types of authigenic carbonate mounds are studied: those within an active hydrothermal field related to serpentinite protrusions in the zone of intersection of a transform fracture zone and the Mid-Atlantic Ridge, and those in an active field of methane seepings in the Dnieper canyon of the Black sea. The general geochemical conditions under which authigenic carbonate formation occurs in the two fields considered were found. They include the presence of reduced H2S, H2, and CH4 gases at the absence of free oxygen; the high alkalinity of the waters participating in the carbonate formation; the similarity of the textural and structural features of authigenic aragonite, which represents the initial mineral of the carbonate matter of the mounds; the paragenesis of aragonite with sulfide minerals; and the close relation of carbonate mounds with communities of sulfate-reducing and methane-oxidizing microorganisms. A new mechanism of formation of hydrothermal authigenic carbonates is suggested; it implies their microbial sulfate reduction over the hydrogen of the fluid in the subsurface zone (biosphere) of mixing between the hydrothermal solution and the adjacent seawater. 相似文献
20.
The lacustrine black shales in the Chang7 Member from the Upper Triassic Yanchang Formation of the Ordos Basin in Central China are considered one of the most important hydrocarbon source rocks. However, the mechanism of organic accumulation in the black shales remains controversial. To resolve the controversy, with the former paleontological data of Yanchang Formation and sedimentation rate data of the Chang7 black shales, we investigated the typical intervals of the Chang7 black shales (TICBS) which were obtained by drilling in Yaowan at the southern margin of the Ordos Basin and performed various sedimentary, isotopic and geochemical analysis, including the sedimentary petrography, pyrite morphology, total organic carbon (TOC) and total sulfur (TS), the ratio of pyritic Fe to total Fe (DOPT), major and trace elements, together with pyritic sulfur isotopes (δ34Spy). The high sulfur content, enrichment of redox-sensitive trace metals, and the lower sedimentation rate of the TICBS in addition to the presence of marine spined acritarchs and coelacanth fossils indicate that the TICBS were deposited in a lacustrine environment possibly influenced by seawater. The petrographic observations show a thick layer of black shale with interlayers of thin layered siltstone (silty mudstone) and laminated tuff, which were related to the turbidity currents and volcanism, respectively. The U/Th, C-S, and Mo-U covariations, pyrite morphology, DOPT, combined with the δ34Spy, suggest that the deposition occurred beneath the anoxic-sulfidic bottom waters, which was intermittently influenced by the oxygen-containing turbidity. The Ni/Al and Cu/Al possibly show extremely high to high primary productivity in the water column, which might be connected with the substantial nutrients input from seawater or frequently erupted volcanic ash entering the lake. In addition, the coincidence of an increased abundance of TOC with increased P/Al, Ni/Al, Cu/Al and U/Th, as well as relatively consistent Ti/Al suggest that the accumulation of the organic matter might be irrelevant to the clastic influx, and was mainly controlled by the high primary productivity and anoxic-sulfidic conditions. Further, the covariations of TOC vs. P/Al and TOC vs. Ba/Al indicate that the high primary productivity led to the elevated accumulation and burial of organic matter, while the anoxic to sulfidic conditions were likely resulted from an intense degradation of the organic matter during the early diagenesis. In summary, the organic matter accumulation is ultimately attributed to the high primary productivity possibly resulted from seawater or volcanic ash entering the lake. 相似文献