Hongxiang Guan

Coupled carbon and sulfur isotope behaviors and other geochemical perspectives into marine methane seepage

Methane seepage is the signal of the deep hydrocarbon reservoir. The determination of seepage is significant to the exploration of petroleum, gas and gas hydrate. The seepage habits microbial and macrofaunal life which is fueled by the hydrocarbons, the metabolic byproducts facilitate the precipitation of authigenic minerals. The study of methane seepage is also important to understand the oceanographic condition and local ecosystem. The seepage could be active or quiescent at different times. The geophysical surveys and the geochemical determinations reveal the existence of seepage. Among these methods, only geochemical determination could expose message of the dormant seepages. The active seepage demonstrates high porewater methane concentration with rapid SO42– depleted, low H2S and dissolved inorganic carbon (DIC), higher rates of sulfate reduction (SR) and anaerobic oxidation of methane (AOM). The quiescent seepage typically develops authigenic carbonates with specific biomarkers, with extremely depleted 13C in gas, DIC and carbonates and with enriched 34S sulfate and depleted 34S pyrite. The origin of methane, minerals precipitation, the scenario of seepage and the possible method of immigration could be determined by the integration of solutes concentration, mineral composition and isotopic fractionation of carbon, sulfur. Numerical models with the integrated results provide useful insight into the nature and intensity of methane seepage occurring in the sediment and paleooceanographic conditions. Unfortunately, the intensive investigation of a specific area with dormant seep is still limit. Most seepage and modeling studies are site-specific and little attempt has been made to extrapolate the results to larger scales. Further research is thus needed to foster our understanding of the methane seepage.

Methane seepage in the Shenhu area of the northern South China Sea: constraints from carbonate chimneys

Two authigenic carbonate chimneys were recovered from the Shenhu area in the northern South China Sea at approximately 400 m water depth. The chimneys’ mineralogy, isotopic composition, and lipid biomarkers were studied to examine the biogeochemical process that induced the formation of the chimneys. The two chimneys are composed mostly of dolomite, whereas the internal conduits and semi-consolidated surrounding sediments are dominated by aragonite and calcite. The specific biomarker patterns (distribution of lipids and their depleted δ13C values) indicate the low occurrence of methanotrophic archaea ANME-1 responsible for the chimneys’ formation via anaerobic oxidation of methane. A significant input of bacteria/planktonic algae and cyanobacteria to the carbon pool during the precipitation of the carbonate chimneys is suggested by the high contributions of short-chain n-alkanes (69% of total hydrocarbons) and long-chain n-alcohols (on average 56% of total alcohols). The oxygen isotopic compositions of the carbonate mixtures vary from 3.1‰ to 4.4‰ in the dolomite-rich chimneys, and from 2.1‰ to 2.5‰ in the internal conduits, which indicates that they were precipitated from seawater-derived pore waters during a long period covering the last glacial and interglacial cycles. In addition, the mixture of methane and bottom seawater dissolved inorganic carbon could be the carbon sources of the carbonate chimneys.

Early Diagenesis Records and Pore Water Composition of Methane-Seep Sediments from the Southeast Hainan Basin, South China Sea

Several authigenic minerals were identified by XRD and SEM analyses in shallow sediments from the Southeast Hainan Basin, on the northern slope of South China Sea. These minerals include miscellaneous carbonates, sulphates, and framboidal pyrite, and this mineral assemblage indicates the existence of gas hydrates and a methane seep. The assemblage and fabric features of the minerals are similar to those identified in cold-seep sediments, which are thought to be related to microorganisms fostered by dissolved methane. Chemical composition of pore water shows that the concentrations of SO42-, Ca2

Methane seepage intensities traced by sulfur isotopes of pyrite and gypsum in sediment from the Shenhu area, South China Sea

The northern slope of the South China Sea is a gas-hydrate-bearing region related to a high deposition rate of organic-rich sediments co-occurring with intense methanogenesis in subseafloor environments. Anaerobic oxidation of methane (AOM) coupled with bacterial sulfate reduction results in the precipitation of solid phase minerals in seepage sediment, including pyrite and gypsum. Abundant aggregates of pyrites and gypsums are observed between the depth of 667 and 850 cm below the seafloor (cmbsf) in the entire core sediment of HS328 from the northern South China Sea. Most pyrites are tubes consisting of framboidal cores and outer crusts. Gypsum aggregates occur as rosettes and spheroids consisting of plates. Some of them grow over pyrite, indicating that gypsum precipitation postdates pyrite formation. The sulfur isotopic values (δ34S) of pyrite vary greatly (from–46.6‰ to–12.3‰ V-CDT) and increase with depth. Thus, the pyrite in the shallow sediments resulted from organoclastic sulfate reduction (OSR) and is influenced by AOM with depth. The relative high abundance and δ34S values of pyrite in sediments at depths from 580 to 810 cmbsf indicate that this interval is the location of a paleo-sulfate methane transition zone (SMTZ). The sulfur isotopic composition of gypsum (from–25‰ to–20.7‰) is much lower than that of the seawater sulfate, indicating the existence of a 34S-depletion source of sulfur species that most likely are products of the oxidation of pyrites formed in OSR. Pyrite oxidation is controlled by ambient electron acceptors such as MnO2, iron (III) and oxygen driven by the SMTZ location shift to great depths. The δ34S values of gypsum at greater depth are lower than those of the associated pyrite, revealing downward diffusion of 34S-depleted sulfate from the mixture of oxidation of pyrite derived by OSR and the seawater sulfate. These sulfates also lead to an increase of calcium ions from the dissolution of calcium carbonate mineral, which will be favor to the formation of gypsum. Overall, the mineralogy and sulfur isotopic composition of the pyrite and gypsum suggest variable redox conditions caused by reduced seepage intensities, and the pyrite and gypsum can be a recorder of the intensity evolution of methane seepage.

Alcohol compounds in Azolla imbricata and potential source implication for marine sediments

This study investigated the composition of long-chain alkyl diols, triols, sec-alcohols, hydroxyl acids, and other hydroxylated compounds in Azolla imbricata and compared the organic alcohol components of Azolla filiculoides, Azolla microphylla, and South China Sea (SCS) sediments in order to investigate the possible indication of Azolla being the biological source of diols and triols in SCS sediment. Large amounts of diols, monohydroxy acids, and sec-alcohols with internal hydroxy groups at ω20 were detected in the three types of Azolla. Among these, 1,ω20-diol and ω20-hydroxy acid exhibited strong even-odd predominance distribution, whereas ω20-sec-alcohol exhibited strong odd-even predominance distribution. In addition, small amounts of diols, triols, and dihydroxy acids with internal hydroxy groups at 9, 10 or ω9, ω10 were detected, among which the chain length of C29 was predominate. Compounds having similar structures as those in Azolla reflected a similar biosynthetic pathway: ω20-hydroxy acid exhibiting even-odd predominance distribution is decarboxylated to ω20-sec-alcohol exhibiting odd-even predominance distribution and converted to 1, ω20-diol with even-odd predominance distribution by acyl reduction; ω9, ω10-hydroxy acid is converted to 1,20,21(1, ω9, ω10)-triol by acyl reduction, and then converted to 9,10-diol by hydrogenation and dehydration. The alcohol components in A. imbricata were clearly not the biological source of 1,13/1,14/1,15-C28, 30, 32 diols and 1,3,4-C27-29 triols in the SCS sediment. Certain marine diatoms might be the source of 1,14-C28, 30 diol in inshore sediment, but the biological source of diols and triols in the SCS sediment requires further investigation.