南海北部油气缓释环境沉积物脂类化合物组成特征

认识沉积环境有机碳留存状况是阐述油气形成过程中有机碳早期成岩的关键内容。以南海珠江口盆地及其邻近海域为背景,通过研究表层沉积物中脂类化合物的形态组成,认识脂类有机碳的来源和留存状态,阐述特征脂类分子的早期成岩特征。结果表明,研究区域表层沉积物有机碳含量为0.22%～0.66%,有机碳稳定同位素分布在-20.88‰～-22.93‰之间,表现为显著的海源特征。沉积物中共检测出21种脂肪酸、6种脂肪醇、8种甾醇和植醇;总脂肪酸、脂肪醇、甾醇和植醇含量分别为12.57～40.27μg/g、5.35～8.98μg/g、0.15～3.75μg/g和0.01～3.99μg/g干重,总体表现为靠近珠江口和台湾海峡略高。脂类化合物的存在形态以游离态(FR)和碱性水解态(BH)为主,酸性水解态(AH)贡献较低;其中植醇和甾醇呈现显著的BH优势,植醇中未检出AH组分的贡献。脂类化合物主要来自于海洋现场生产,海洋微藻和细菌的相对贡献率分别为21.18%～33.78%和11.02%～15.64%,陆源高等植物贡献低于5%。来源于硫酸盐还原菌的支链脂肪酸在靠近珠江口海域高达1.79～2.62μg/g,占总脂肪酸的5.14%～6.50%,并与硫酸盐还原过程相关的古菌分布相一致。     

From land to sea: provenance,composition, and preservation of organic matter in a marine sediment record from the North-East Greenland shelf spanning the Younger Dryas–Holocene

The organic matter content of marine sediments is often used to infer past changes in ocean conditions. However, the organic carbon pool preserved in coastal sediments is a complex mixture derived from different sources and may not reflect in situ processes. In this study, we combine taxonomic identification of reworked palynomorphs with pyrolysis organic geochemistry and reflected-light organic petrographic microscopy to investigate the provenance, composition and preservation of organic matter in a marine sediment core retrieved from the NE Greenland shelf. Our study reveals continuous yet variable input of land-derived organic carbon to the marine environment throughout the late Younger Dryas–Holocene, with the highest input of inert carbon in the late Younger Dryas. Although the sediments contain some recent marine palynomorphs, there is no other evidence of fresh marine organic carbon. In contrast, our results indicate that these shelf sediments represent a significant sink of recycled organic carbon. The results of pyrolysis geochemistry revealed that ~90% of the total organic carbon in the sediments is inert. The organic petrography analyses revealed that >70–84% of the organic carbon in the sediment core is terrigenous. Reworked dinoflagellate cysts showed a continuous provenance of Cretaceous land-derived material, most likely from the nearby Clavering Island. Our study points to the importance of constraining the organic matter origin, composition and preservation in marine sediments to achieve more accurate palaeoenvironmental reconstructions based on organic proxies.     

Geological environment of a methane-rich Recent sedimentary basin in the Gulf of St. Lawrence

Two sediment cores collected in Chaleur Trough, Gulf of St. Lawrence are compared in terms of organic geochemistry, sediment texture and foraminifera. One of the cores was collected from a depression and contained methane in the range of 5,970–14,230 ppm, in comparison to 42–106 ppm in the core of open environment. The sediments of the methanerich core are finer, higher in organic carbon, extractable organic matter, plant pigments and contained more diverse foraminiferal assemblages. The results of these geological investigations tend to suggest a relatively fast rate of sedimentation in the depression. This results in the preservation of organic compounds and development of anaerobic subsurface conditions, consequently giving rise to high concentrations of methane through fermentative processes. No other gaseous hydrocarbons were detected hence the possibility of seepage of petroleum gases appears to be remote.     

Sterol geochemistry of sediments from the western North Atlantic Ocean and adjacent coastal areas

Core sections from coastal bay, continental slope, and continental rise surface sediments of the western North Atlantic were analyzed for sterols. Changing rate or type of sediment input, bioturbation, and chemical conversion appear to be processes important in controlling the distribution of sterols in these sediments. Comparisons of individual sterol distributions and variations in the ratio of Soxhlet-extractable to non-extractable saponified sterols indicate that for the western North Atlantic, the extent to which each process is dominant varies with proximity to shore. Evidence is presented to show that sterols in the deep sea may be at least partially terrigenous in origin and not all biogenically derived in the surface waters. These sterols, and by analogy other labile organic compounds, may serve as a source of carbon for benthic organism metabolism.     

http://www.sciencedirect.com/science/article/pii/S1674987111001307

South China Sea(SCS) is the largest Western Pacific marginal sea.However,microbial studies have never been performed in the cold seep sediments in the SCS.In 2004."SONNE" 177 cruise found two cold seep areas with different water depth in the northern SCS.Haiyang 4 area,where the water depth is around 3000 m.has already been confirmed for active seeping on the seafloor.such as microbial mats,authigenic carbonate crusts and bivalves.We investigated microbial abundance and diversity in a 5.55-111 sediment core collected from this cold seep area.An integrated approach was employed including geochemistry and 16S rRNA gene phylogenetic analyses.Here,we show that microbial abundance and diversity along with geochemistry profiles of the sediment core revealed a coupled reaction between sulphate reduction and methane oxidation.Acridine orange direct count results showed that microbial abundance ranges from 10~5 to 10~6 cells/g sediment(wet weight).The depth-related variation of the abundance showed the same trend as the methane concentration profile.Phylogenetic analysis indicated the presence of sulphate-reducing bacteria and anaerobic methane-oxidizing archaea.The diversity was much higher at the surface,but decreased sharply with depth in response to changes in the geochemical conditions of the sediments,such as methane,sulphate concentration and total organic carbon.Marine Benthic Group B.Chloroflexi and JSl were predominant phylotypes of the archaeal and bacterial libraries,respectively.     

Petroleum Geology in Deepwater Settings in a Passive Continental Margin of a Marginal Sea: A Case Study from the South China Sea

Deepwater oil and gas exploration has become a global hotspot in recent years and the study of the deep waters of marginal seas is an important frontier research area.The South China Sea(SCS)is a typical marginal sea that includes Paleo SCS and New SCS tectonic cycles.The latter includes continental marginal rifting,intercontinental oceanic expansion and oceanic shrinking,which controlled the evolution of basins,and the generation,migration and accumulation of hydrocarbons in the deepwater basins on the continental margin of the northern SCS.In the Paleogene,the basins rifted along the margin of the continent and were filled mainly with sediments in marine-continental transitional environments.In the Neogene–Quaternary,due to thermal subsidence,neritic-abyssal facies sediments from the passive continental margin of the SCS mainly filled the basins.The source rocks include mainly Oligocene coal-bearing deltaic and marine mudstones,which were heated by multiple events with high geothermal temperature and terrestrial heat flow,resulting in the generation of gas and oil.The faults,diapirs and sandstones controlled the migration of hydrocarbons that accumulated principally in a large canyon channel,a continental deepwater fan,and a shelf-margin delta.     

Bacterial hopanoids as tracers of organic carbon sources and processing across the western Arctic continental shelf

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

CN ratios in Pacific deep-sea sediments: Effect of inorganic ammonium and organic nitrogen compounds sorbed by clays

Analyses of organic carbon, total nitrogen, and inorganically bound ammonium (exchangeable and fixed ammonium) in two oxic deep-sea sediment cores from the Central Pacific Ocean revealed insufficiently high inorganic ammonium contents of these sediments to explain the low C/N ratios, although representing 20–45% of the total nitrogen.Both, organic carbon/total nitrogen ratios (ranging from 3.9?1.3) and organic carbon/organic nitrogen ratios (5.6?1.9) decrease with increasing sediment depth, the latter indicating a real enrichment of organic nitrogen compounds during diagenesis relative to total organic matter.Organic matter/alumina relationships indicate that this unusual preservation of organic nitrogen compounds is probably caused by sorption to clay minerals protecting them against bacterial attack.     

Spectroscopic and Chromatographic studies of organic carbon in Recent marine sediments from the Peruvian Upwelling Zone

Early diagenesis of organic matter in sediments from two sites in the Peruvian Upwelling Zone (12°05′S, 77°39′W; 15°17′S, 75°24′W) has been studied by observing changes in the total organic carbon and lipid and humin fractions with depth. Transformations of the total carbon and humin fraction have been characterized by conventional and time-dependent solid state NMR techniques, while lipid diagenesis was monitored by measuring the concentration of sterols in the same sedimentary horizons. Both the quantity of total sterols and the relative abundances of individual sterols vary with sampling location, suggesting a difference in the input of biomass to the sediments at the two sites. Total sterol concentrations decrease with depth at both sites, but the loss of sterols occurs much more slowly at the more anoxic northern site, where sedimentation rates and organic carbon contents are approximately twice those at the southern site. ¹³C-NMR spectra of the total organic carbon and the humin fraction suggest that humin-like compounds are an original component of the sedimentary biomass, and dipolar-dephased spectra of the humin residue indicate that diagenetic alterations of the humin fraction are occurring even in these very young sediments. Conventional and time-dependent spectroscopic data support the hypothesis that humin formation results from selective preservation of microbially-resistant biopolymers which are an original component of the sedimentary biomass combined with loss of certain labile compounds.     

南海表层沉积物中放射虫的组合特征与海洋环境

南海拥有较齐全的边缘海地理地貌与生态环境, 沉积物中保存的放射虫种类繁多, 个体丰富.本文采用数理统计与聚类分析方法, 对表层沉积物中放射虫的组合特征进行了较为详细的定量分析, 以期获得可靠的放射虫组合与分布的特征.聚类分析结果显示, 放射虫组合在南海表层沉积物中的分布大致可区分为5种类型: 陆架浅水区型、陆坡珊瑚礁区型、中央海盆区型、南部富营养区型和夏季上升流区型, 它们分别对应于特有的海洋环境, 并由含有某些优势种类的放射虫群落所组成.进一步分析还表明, 南海的北部、中部和南部分别表现为3个不同生态环境的海区: 北部海区受陆源影响较为明显; 中部海区被中央水团、海底火山活动和夏季上升流活动所控制; 南部海区总体上属于典型的珊瑚礁海洋环境, 生态与沉积环境明显优越于北部海区.南海表层沉积物中放射虫的组合分布特征较好地响应和反映了所在海区的生态环境与沉积条件, 是探讨古海洋环境的重要依据.      

Role of a strong oxygen-deficient zone in the preservation and degradation of organic matter: a carbon budget for the continental margins of northwest Mexico and Washington State

Rates of organic carbon oxidation in marine sediments were determined for the continental margins of northwest Mexico and Washington State, with the goal of assessing the role of oxygen in the preservation of organic matter on a margin with a strong oxygen-deficient zone and on a typical western continental margin. Total carbon oxidation rates (including rates for individual electron acceptors: O₂, NO₃⁻, and SO₄⁼) were determined at depths ranging from 100 to 3000 m on both margins. Carbon oxidation rates were generally higher on the Washington margin than on the Mexican margin. The relative importance of the different electron acceptors varied across the two margins and was related primarily to the availability of O₂ and NO₃⁻ from the overlying water. The relative contribution of O₂ consumption increased in deeper sediments (>2000 m) as aerobic processes began to dominate the total carbon oxidation rate. Denitrification rates were highest in Washington sediments; however, denitrification represented a larger fraction of the total carbon oxidation rate in the Mexican sediments (∼40% for Mexico vs. ∼30% for Washington). Sulfate reduction accounted for as much as 79% of the total carbon oxidation rate in shallow sediments and less than 20% in deep sediments on both margins. The offshore trends in carbon oxidation rate appeared to be related to the organic carbon input rate. Pore-water O₂ and NO₃⁻ penetration depths were shallowest in nearshore stations and increased offshore. Regeneration ratios of C:N:P reveal “non-Redfield” behavior on both margins. Carbon budgets for the two margins demonstrate that off Mexico, a much greater percentage of the organic matter produced in the surface ocean reached the sediments (>15% vs. <8% for Mexico and Washington, respectively). On the Mexican margin, ∼8% of the primary production escaped oxidation in the surface sediments to be permanently buried, as compared with only ∼1.2% of the primary production on the Washington margin. This suggests that oxygen-deficient conditions on Mexican margin are linked to enhanced carbon preservation.     

Fecal Sterols in Estuarine Sediments as Markers of Sewage Contamination in the Cubat?o Area, S?o Paulo, Brazil

Sterol biomarkers serve as an alternative method for detecting sewage pollution. Sterols were extracted from samples of surface sediment collected in Cubat?o (the Vila dos Pescadores and Vila Esperan?a communities) and quantified using GC–MS after Soxhlet extraction, cleanup, and derivatization. Fecal contamination was evaluated based on the concentration of coprostanol and the ratio of the selected sterols. The most abundant sterol was cholestanol, followed by coprostanol. The concentrations of coprostanol in surface sediments ranged from a minimum of 4.21?μg?g^?1 dry sediment (Vila dos Pescadores station) to a maximum of 8.32?μg?g^?1 dry sediment (Vila Esperan?a station). A coprostanol concentration of about 10?μg?g^?1 was found, indicating areas of high sewage contamination. Coprostanol levels at sewage stations were higher than in other Brazilian coastal areas, which may be attributed to the fraction of the population without sanitation services.     

Geochemical insights into contribution of petroleum hydrocarbons to the formation of hydrates in the Taixinan Basin,the South China Sea

Methane hydrate in the South China Sea(SCS)has extensively been considered to be biogenic on the basis of itsδ13C and δD values.Although previous efforts have greatly been made,the contribution of thermogenic oil/gas has still been underestimated.In this study,biomarkers and porewater geochemical parameters in hydrate-free and hydrate-bearing sediments in the Taixinan Basin,the SCS have been measured for evaluating the contribu-tion of petroleum hydrocarbons to the formation of hydrate deposits via a comparative study of their source inputs of organic matters,environmental conditions,and microbial activities.The results reveal the occurrence of C14-C16 branched saturated fatty acids(bSFAs)with relatively high concentrations from sulfate-reducing bacteria(SRBs)in hydrate-bearing sediments in comparison with hydrate-free sediments,which is in accord with the positive δ13C values of dissolved inorganic carbon(DIC),increasing methane concentrations,decreasing alka-linity,and concentration fluctuation of ions(Cl-,Br,SO2-,Ca2+,and Mg2+).These data indicate the relatively active microbial activities in hydrate-bearing sediments and coincident variations of environmental conditions.Carbon isotope compositions of bSFAs(-34.0％o to-21.2％o),n-alkanes(-34.5％o to-29.3％o),and methane(-70.7％o to-69.9％o)jointly demonstrate that SRBs might thrive on a different type of organic carbon rather than methane.Combining with numerous gas/oil reservoirs and hydrocarbon migration channels in the SCS,the occurrence of unresolved complex mixtures(UCMs),odd-even predominance(OEP)values(about 1.0),and biomarker patterns suggest that petroleum hydrocarbons from deep oil/gas reservoirs are the most probable carbon source.Our new results provide significant evidence that the deep oil/gas reservoirs may make a contribution to the formation of methane hydrate deposits in the SCS.     

The geochemical significance in early sedimentation of geolipids obtained by saponification of lacustrine sediments

Significant quantities of solvent-inextractable geolipids, obtained by saponification of solvent extracted sediments, were found in various sedimentary samples including soils, river inlet sediment and lake sediments from Lake Suwa.The carbon isotopic composition ($\text{δ}{}^{13}\text{C}$) of extractable and inextractable geolipids from the same sediment sample were similar. Moreover, the carbon number distributions of sterols in the two geolipid fractions from the same sediment were also similar.Whereas the ratios of both lipids and sterols to total organic carbon for the extractable geolipids in the lake sediments decreased with depth, the former ratio for inextractable giolipids tends to increase with depth and the latter remains fairly constant. On the other hand, the stanol to stenol ratio of the extractable fraction increased with depth but that of the inextractable fraction was lower than that of the extractable fraction and was fairly constant irrespective of sediment depth.The transformation of extractable sterols into inextractable ones was not observed during incubation for 1200 days of sterols with Suwa sediments.Thus, the following conclusions were made: (1) the extractable and inextractable geolipids have similar origins, (2) some constituents of the latter may be protected from chemical or microbiological degradation and transformation in the sediments, and (3) the transformation of some constituents of the former into the inextractable ones virtually does not occur after incorporation into Suwa sediments.These results suggest that some constituents of the inextractable geolipid fraction may provide fundamental information on early diagenetic alteration of geolipids in lake sediments and on the relatively recent paleoenvironment.     

Environmental changes in Saginaw Bay,Lake Huron recorded by geolipid contents of sediments deposited since 1800

Changes in organic materials preserved within sediments of Saginaw Bay deposited over the past two centuries record corresponding periods in the environmental history of this part of Lake Huron and its watershed. Sediments deposited since 1940 show an increasingly greater input of aquatic organic matter in response to accelerating cultural eutrophication of Saginaw Bay. Concentrations of fatty acids, sterols, fatty alcohols, and aliphatic hydrocarbons are higher in these modern sediments than in deeper ones. Molecular distributions of these geolipids reflect less aquatic material deeper in the sediments. Prior to 1875, sediment organic matter appears to be diluted by mineral matter from enhanced erosion caused by clearing of the watershed for farming and settlement. During this period there is better preservation of carbonate minerals due to quicker burial. Since 1875, petroleum components comprise over 90% of the total aliphatic hydrocarbon content of these sediments, reflecting the advent and continued existence of chronic, low-level petroleum contamination of this part of the Great Lakes.     

Marine and terrigenous lipids in coastal sediments from the Peru upwelling region at 15°S: Sterols and triterpene alcohols

The distributions of free 4-desmethyl sterols in sediments from the Peru coastal zone at 15°S have been determined. Major free sterols in the surface sediments include cholesterol, which is mainly derived from zooplankton, and two C₂₈ sterols: 24-methylcholesta-5,24(28)-dien-3β-ol and 24-methylcholesta-5,22E-dien-3β-ol both of which are derived fro diatoms. Their concentrations decrease by almost an order of magnitude in the top 20 cm of sediment depth, indicating that free sterols are rapidly degraded in this sedimentary environment. Lipids from higher plants were also detected: long chain fatty acids and alcohols and various triterpenoid alcohols, including taraxerol, lupeol and α- and β-amyrin. The concentrations of most terrigenous lipids varied by less than a factor of 3 over the same depth, and these changes were not correlated with changes in the concentrations of total organic carbon. Below 3 cm, lipids from higher plants predominated in the extractable lipid distributions due to the more rapid degradation of marine lipids. We postulate that there are significant marine sources of the higher plant sterols 24-ethylcholesterol, 24-ethylcholesta-5,22E-dien-3β-ol and 24-methylcholesterol in these sediments. A high proportion of many of the terrigenous lipids in these sediments are probably transported into the coastal zone by rivers, rather than from the atmosphere, and then redistributed by bottom currents.     

Carbon–sulfur–iron relationships in sedimentary rocks from southwestern Taiwan: influence of geochemical environment on greigite and pyrrhotite formation

The importance of the magnetic iron sulfide minerals, greigite (Fe₃S₄) and pyrrhotite (Fe₇S₈), is often underappreciated in geochemical studies because they are metastable with respect to pyrite (FeS₂). Based on magnetic properties and X-ray diffraction analysis, previous studies have reported widespread occurrences of these magnetic minerals along with magnetite (Fe₃O₄) in two thick Plio-Pleistocene marine sedimentary sequences from southwestern Taiwan. Different stratigraphic zones were classified according to the dominant magnetic mineral assemblages (greigite-, pyrrhotite-, and magnetite-dominated zones). Greigite and pyrrhotite are intimately associated with fine-grained sediments, whereas magnetite is more abundant in coarse-grained sediments. We measured total organic carbon (TOC), total sulfur (TS), total iron (Fe_T), 1N HCl extractable iron (Fe_A), and bulk sediment grain size for different stratigraphic zones in order to understand the factors governing the formation and preservation of the two magnetic iron sulfide minerals. The studied sediments have low TS/Fe_A weight ratios (0.03–0.2), far below that of pyrite (1.15), which indicates that an excess of reactive iron was available for pyritization. Observed low TS (0.05–0.27%) is attributed to the low organic carbon contents (TOC=0.25–0.55%), which resulted from dilution by rapid terrigenous sedimentation. The fine-grained sediments also have the highest Fe_T and Fe_A values. We suggest that under conditions of low organic carbon provision, the high iron activity in the fine-grained sediments may have removed reduced sulfur so effectively that pyritization was arrested or retarded, which, in turn, favored preservation of the intermediate magnetic iron sulfides. The relative abundances of reactive iron and labile organic carbon appear to have controlled the transformation pathway of amorphous FeS into greigite or into pyrrhotite. Compared to pyrrhotite-dominated sediments, greigite-dominated sediments are finer-grained and have higher Fe_A but lower TS. We suggest that diagenetic environments with higher supply of reactive iron, lower supply of labile organic matter, and, consequently, lower sulfide concentration result in relatively high Eh conditions, which favor formation of greigite relative to pyrrhotite.     

青海湖底沉积物的矿物物相及有机质保存研究

盐湖沉积环境是烃源岩发育的重要地质环境。本文以青海湖湖底沉积物为例，根据有机质与粘土矿物含最及矿物表面积的关系，分析了矿物学因素对盐湖相富有机质沉积物中有机质保存的影响。研究发现：湖底沉积物中有机质丰富，为上层水中的浮游生物和南河流携带束的陆地高等植物两种来源。矿物物相分析发现沉积物中粘土矿物含量达到32．4％，以伊利石为主。沉积物经密度分离后测试发现，有机碳含量与粘土矿物含量及矿物表面积之间具有很好的正相关性，说明粘土矿物吸附是青海湖底沉积物中有机质的主要赋存形式。     

Matrix protected organic matter in a river dominated margin: A possible mechanism to sequester terrestrial organic matter?

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

Sources and distributions of tetraether lipids in surface sediments across a large river-dominated continental margin

Glycerol dialkyl glycerol tetraether (GDGT)-based proxies are increasingly used in modern carbon cycling and palaeoenvironmental investigations. It is therefore crucial to examine the robustness (sources, transport and degradation) of all GDGT-based proxies in continental margins, where sedimentation rates and extent of carbon cycling are high. We have analyzed the distributions of GDGTs in surface sediments from the Lower Yangtze River and East China Sea (ECS) shelf. The results revealed multiple sources and complex shelf processes that govern the distributions. The isoprenoid GDGT-inferred sea surface temperatures (SSTs) are robust and reflect the satellite-derived annual mean SSTs on the shallow ECS shelf, confirming an origin from surface water column-dwelling crenarchaeota. The input from methanogen-sourced, isoprenoid GDGTs is significant in the river surface sediments but they are almost absent from the ECS shelf. Branched GDGTs are also abundant in the river sediments, but ca. 95% are degraded in the Yangtze estuary, a much greater extent than observed for other terrigenous organic matter (OM) proxies. There is also evidence for production of branched GDGTs in the oxic ECS shelf water column and the anoxic sediments/waters of the Lower Yangtze River. As a result, branched GDGT-based proxies in the lower river and ECS surface sediments do not reflect the catchment environmental conditions. The effective degradation in the estuary and widespread aquatic contributions of branched GDGTs improves our understanding of how to use branched GDGT-based proxies in marginal seas.