Carbon Isotopic Composition Research Articles

Carbon and nitrogen biogeochemistry of a high-altitude Himalayan lake sediment: Inferences for the late Holocene climate

A study was conducted to decipher changes in paleoenvironmental conditions of the Kashmir Valley (India) using stable isotopic compositions and elemental concentrations of total organic carbon (TOC) and total nitrogen (TN) in a sediment core from the Wular Lake. The Chronology of the core established through radiocarbon dating estimated the age of the core bottom to be 3752 Cal years BP, covering the late Holocene. Using carbon isotopic compositions of TOC (δ13C), nitrogen isotopic compositions of TN (δ15N), and TOC - TN contents, the study identified changes in biology and associated biogeochemical processes in the Wular Lake during the late Holocene. Changes in C and N biogeochemistry of the lake through the last 3752 Cal years BP suggested overall drier condition during 3752–1500 Cal years BP that transitioned into a wetter condition at around 1500 Cal years BP until at least 295 Cal years BP. Evidence for relatively intense drier events were observed within the dry and wet phases at around 2500 and 500 Cal years BP. Changes in δ13C and TOC contents in the sediment core revealed that the inorganic C dynamics and productivity (along with organic C contents) in the lake were largely regulated by variations in respired CO2 and HCO3− availability along with terrestrial matter supply through the Jhelum River. Similarly, variations in δ15N and TN contents showed changes in N dynamics of the lake with varying nitrification and decomposition throughout the studied period. Observed dry and wet phases in the region might be due to the weakening and strengthening of the precipitation, which was linked to negative and positive phases of the North Atlantic Oscillation, respectively.

Using isotope-geochemical criteria for Olympiadinskoye gold deposit gas system genesis diagnosis

The authors studied modern gas manifestations spatially associated with the ore deposits in the Kaitbinskaya lithological-facies zone of the Yenisei Ridge. The purpose of the research is to obtain scientifically based data on the genesis of gaseous and vaporous fluids in various sampling environments of the Vostochny open-pit mine of the Olympiadinskoye gold deposit: rocks, natural waters, free-flowing gases from blastholes and air of the surface atmosphere. It has been conducted a complex of field and analytical works including degassing, gas chromatography, pyrolysis of the organic substance of lithified and metamorphosed deposits, analysis of carbon isotopic composition in carbon dioxide and methane in fluidal systems. In order to study normal gas-geochemical field (natural background) of the work area an atmospheric geochemical survey was carried out at the reference site – an “environmentally friendly” site with the minimal influence of technogenic factors. It has been determined that the surface atmosphere of the site had been formed due to the landscape and geomorphological conditions of the Kaitbinskaya lithological-facies zone as well as fluidal systems of deep horizons. The latter, due to the presence of an extensive network of disruptive disturbances and diffusion-filtration processes of mass transfer reached the zone of exploratory geochemical sounding. The conducted pyrolytic studies of rocks have proved that within the open section of the Vostochny open-pit mine the organic substance of the Kordinskaya series of the lower Riphean deposits has implemented its oil and gas generation potential and cannot serve the formation source of abnormal gas fields of the Olympiadinskoye gold deposit. The studied gas systems are polygenic in nature and, being allochthonous to the host sediments, are formed without the participation of gases from the upper generating (bio) zone. According to isotope-geochemical criteria, these are mainly endogenous and naphthidogenic fluids identical to the gas condensate accumulations of the Yurubcheno-Tokhomskaya oil and gas accumulation zone.

Tracing Oils and Gas Accumulation in Complex Petroleum Systems Based on Biomarkers, Light Hydrocarbons, and Diamondoids from Concomitant Crude Oils: A Case Study in the Shawan Sag of the Junggar Basin, NW China.

The Shawan Sag is one of the most promising blocks in the western Junggar Basin for natural gas and oil exploration. To date, the research and exploration degree here is still low, and there is limited understanding of the origin and migration of natural gas and oils, which seriously restricts future exploration and development. At least three oil charging episodes and one gas charging episode could be confirmed in the reservoirs on the western slope of the Shawan Sag based on the analysis of concentrations and ratios of hopanes and steranes, diamondoids, and light hydrocarbons. The first and second charging oils originated from the peak and late oil generation window stages of Lower Permian Fengcheng Formation (P1f) source rocks, respectively. The third charging oil originated from the late oil generation window stage of source rocks of the Middle Permian lower Wuerhe Formation (P2w). Combining the carbon isotopic compositions and the gas composition, the fourth charging gas was derived from the postmature source rocks of Carboniferous(C) and Lower Permian Jiamuhe Formation (P1j) and the high-postmature source rock of Lower Permian Fengcheng Formation (P1f). The preservation conditions of nature gas in the Mesozoic (T-K) cap rocks in the Shawan Sag, as indicated by methyladamantanes (MAs)/methyldiamantanes (MDs) ratio, are better than those in the Mahu Sag. In this study, the methyladamantane maturity parameters of oils in the reservoirs were proposed to evaluate the maturity and further determine the migration direction of late-charging natural gas. The results suggest that late postmatured natural gases were charged from the southern part to the northwest of the Shawan Sag. Therefore, the southeastern direction of Well SP1 is a favorable area for natural gas exploration in the Shawan Sag. Meanwhile the northern part of the sag is favorable for the exploration of high-mature oil generated from source rocks within the Middle Permian Lower Wuerhe Formation.

The Measurement Reliability of δ13C of Dissolved Organic Carbon: A Validation for Speleothem Samples

The carbon isotopic composition of dissolved organic carbon (δ13CDOC) in speleothems, based on high-precision U-Th ages, has great potential to reconstruct past ecology, microbial activity, and carbon cycling. Identifying the reliability of the pretreatment and measurement of speleothem δ13CDOC is therefore essential to putting it into practice. Actually, we have previously verified the reliability of the method for speleothem δ13CDOC measurements. However, it was only based on the final δ13CDOC values of homogeneous speleothem powder and is unable to evaluate the effects of different experimental conditions and the impacts of adding acid on δ13CDOC if using speleothem as the study samples. In this study, we used an organic reagent (potassium sorbate) as the study sample and designed a conditional experiment that simulates the protocols for speleothem δ13CDOC analysis and presented the resulting data to inspect the effects of the experimental processes on the analysis of δ13CDOC. The results show that the standard deviation of duplicate samples is 0.1‰, which is close to that of the previous work for organic reagents and water samples, and the results were not affected by different experimental conditions and operation steps (such as adding orthophosphoric acid, digestion time, and storage duration of resulting CO2 in storage vessels), suggesting that this method is robust to detect the speleothem δ13CDOC. Considering the range and standard deviation of results, we proposed that the δ13CDOC record could be used in various studies when the amplitudes of the δ13CDOC record are larger than 0.1‰, especially greater than 0.4‰.

The Carbon Isotopic Composition of Archean Kerogen and Its Resilience Through the Rock Cycle

The Archean rock record is limited and there is minimal organic matter available to understand the origin and evolution of life on early Earth. Low carbon isotope ratios have been measured in organic and reduced carbon phases in Archean rocks and have been invoked as biosignatures. However, it can be challenging to distinguish whether these low values reflect biotic formation, abiotic reactions, or post-depositional processes. To re-address this long-standing question, we compiled a comprehensive dataset of carbon isotope ratio measurements from organic carbon phases from Archean units that were analyzed using a variety of geochemical techniques. Our compilation also includes available descriptions and measurements of the stratigraphy, mineralogy, elemental ratios, and metamorphic grade for each data point. Our statistical analyses re-enforce a result that has been noted by prior compilations, that the carbon isotopic composition of Archean organic matter (OM) is broadly more 13C-deplete than the composition of Phanerozoic OM: The median δ13C values ( ±SD) of Archean total organic carbon and kerogen were −30.5±8‰ (n=2421) and −33.7±11.3‰ (n=556; Phanerozoic OM δ13C ±SD = −26.7±4.6‰ with n=449 from a prior compilation). Our study also identifies a previously unrecognized bimodality within the δ13C values of Archean OM that is observed even with subsampling of the data to account for geographic and stratigraphic sampling bias. We describe and model the isotopic and structural changes associated with the transformation of marine Type II kerogen from formation through diagenesis, catagenesis and metagenesis, and metamorphism, as described by trends on a van Krevelin diagram. Empirically, early maturation of organic matter during diagenesis results in shifts up to a few per-mille, which can occur in either direction depending on selective preservation and degradation of compounds. Thermal cracking that occurs during catagenesis can drive increases in δ13C of 5–12‰. At temperatures above greenschist metamorphism, carbon atoms exchange with other reactive carbon pools, driving increases in δ13C of up to 20‰. Together, our analyses suggest that the most metamorphosed graphitic samples from the earliest Archean are likely signatures of alteration, while low and multimodal ranges of δ13C values may preserve records of Archean ecology.

Влияние факторов водной среды на минерализацию цианобактерий и зеленых водорослей (Республика Коми)

This article describes crystallization formed in the exogenous mucous sheath of phototrophic microorganisms living in the surface waters of the south area of the Komi Republic. The mineralization of colonies of cyanobacteria of the Gloeotrichia sp. and green algae Chaetophora elegans was studied. The waters of rivers in the Northern Dvina basin have been studied as habitats for the microorganisms. They have a different composition: HCO3 Ca–Mg, typical for the taiga zone of a temperate continental climate; SO4–HCO3 Ca–Mg and Cl–Na (in the zone of technogenic pollution). Using the example of these neutral — weakly alkaline ultrafresh — salty (0.2—2.8 g/L) waters, it is shown that the geochemistry of the aquatic environment is one of the most important factors influencing the minerogenesis. Calcite, vaterite, quartz and halite were identified in dried colonies of microorganisms within the extracellular polymeric substance using the methods of X-ray diffractometry, electron microscopy, microprobe analysis and IR spectroscopy. The morphological features of microminerals are presented depending on the type of microorganisms. Calcium carbonate crystals and aggregates are formed within the exogenous mucous sheath of algae and cyanophytes. The carbon isotope composition of carbonates (13C –7.5 and –3.8 ‰ PDB) indicates their organic nature. The formation of minerals, morphological features of crystals and the degree of biomineralisation of colonies of phototrophic microorganisms are conditioned by the physicochemical parameters of the aquatic environment. The possibilities of chemogenic precipitation of carbonates from the studied natural waters were assessed.

Stable isotopic composition of Bothrops atrox (common lancehead) in four distinct land covers in eastern Amazonia

AbstractSince consumers reflect the isotopic composition of an assimilated diet, stable isotopes can be a useful tool to address the feeding ecology of tropical snakes. This is the first study reporting carbon and nitrogen stable isotopic composition of Bothrops atrox (Linnaeus, 1758) living in different landscapes located in the lower Amazon river, encompassing four main natural landscapes of the Amazon: old‐growth forests, várzeas (flooded forests), savannas, and pastures. Our null hypothesis is that the δ13C of forest specimens of B.atrox is more negative because forests are dominated by C3 plants, while C4 plants are common in the other landscapes. On the other hand, δ15N of forest specimens should be more positive, since the δ15N of old‐growth forests are higher than plants of savanna, várzea, and pastures. Confirming our hypothesis, the δ13C of B. atrox scales of the Tapajós National Forest was approximate −25‰ to −24‰, increased to approximately −23.5‰ to −23.0‰ in the savanna and pasture, and to −21‰ in the várzea, showing an increased contribution of C4‐derived carbon. Some specimens of B. atrox had δ15N as high as 18‰, which is much higher than the average δ15N of the snake's prey (7‰), confirming the apex position of B. atrox in the Amazon region. The δ15N values of the forest specimens were 5‰ higher than the savanna specimens, and this difference decreased to 3‰ between the forest and the pasture, and the várzea specimens. Finally, there were not large differences between δ15N values of livers and scales in any of the landscapes, suggesting a constant diet through time, and reinforcing the possibility of the use of snake's scale as a less invasive and non‐lethal tissue to analyze.Abstract in Portuguese is available with online material.

Carbon and hydrogen isotopic compositions of C7 hydrocarbons and their geochemical significance in light oils/condensates from the Kuqa Depression, Tarim Basin, NW China

In this study, the geochemical significance of the δ13C and δ2H values of selected C7 light hydrocarbons (nC7 = n-heptane; MCH = methylcyclohexane; Tol = toluene) is investigated in 58 light oil/condensate (LOC) samples from the Kuqa Depression of the Tarim Basin, NW China. For most of the LOCs in the western region, the nC7, MCH, and Tol exhibit systematic differences where δ13CnC7 < δ13CMCH < δ13CTol and δ2HTol < δ2HnC7 < δ2HMCH. LOCs from the eastern area have higher δ13Coil, δ13CTol, and δ13CMCH values than those from the western area and their δ13C values for C7 hydrocarbons are similar and δ2HnC7 < δ2HMCH < δ2HTol. These organic geochemical differences indicate that the LOCs from the western and eastern areas of the Kuqa Depression were mainly derived from lacustrine and coaly parent materials, respectively. The LOC reservoirs generally received a late hydrocarbon charge of the high-maturity natural gas, and the LOCs from the western Kela–Keshen areas subsequently experienced gas leakage. Hierarchical cluster analysis indicates that the most important influencing factor on the LOCs of the Kuqa Depression is the sedimentary facies (coaly and lacustrine), followed by gas leakage and then parent organic type (lacustrine sapropel and humic organic matter). A cross-plot of the Δδ2HTol–MCH versus Tol/MCH can distinguish the origins of continental facies parent materials and gas leakage of the LOCs.

Effects of source facies and maturity on individual carbon isotopic compositions of oil

Carbon isotopes have been used extensively in tracing the sources of oil. However, primary source facies and secondary alteration controls on oil isotopic compositions have not been well resolved, resulting in application uncertainties. A case study was undertaken for an alkaline lacustrine oil system in a lower Permian formation in the Junggar Basin, NW China. Results indicate that increasing maturity causes the carbon isotopic composition to become heavier for only short–middle-chain compounds, whereas source facies-related carbon assimilation controls the compositions of short-, middle-, and long-chain compounds. In particular, light-carbon assimilation during organic-matter degradation makes the isotopic composition lighter, whereas heavy carbon from the water mass makes it heavier. Accordingly, oils in this study area were divided into Type U and Type N oils based on individual compound carbon isotopic compositions, reflecting the difference in source facies in a highly saline and reducing stratified water environment. The results provide a better understanding of the controls on carbon isotopes in oil in sedimentary basins, reducing the uncertainty in oil–source correlation and addressing the origin of oil.

Characterization of carbon and oxygen isotopes of plant on climate and plant physiology at the southeastern margin of Qinghai-Tibet Plateau, China

To investigate the correlation between carbon and oxygen isotope compositions of plant cellulose and climatic factors as well as plant physiological indices on the southeastern margin of the Qinghai-Tibet Plateau, we examined plant species in eight sampling sites with similar latitudes and different longitudes in this region. Through the characteristics of δ13C and δ18O values, fractionation values (Δ13C and Δ18O) in leaf cellulose, we discussed water use efficiency (WUE) and the environmental factors, the variation of carbon and oxygen isotopes in the southeastern margin of the Qinghai-Tibet Plateau with elevation and longitude, and revealed the indication degrees of isotopic signals to different environments and vegetation physiology. By using the semi-quantitative model of carbon and oxygen dual isotopes, we investigated the physiological adaptation mechanisms of plants to varying environmental conditions. The results demonstrated that both Δ13C and Δ18O of cellulose decreased with increasing elevation and longitude, and Δ13C was more influenced by longitude, while Δ18O was more susceptible to elevation variation. Additionally, Δ13C and Δ18O were significantly and positively correlated with temperature (TEM), precipitation (PRE), potential evapotranspiration (PET), and relative humidity (RH). PRE was the dominant meteorological factor driving the variation of Δ13C, while RH was the dominant meteorological factor influencing Δ18O variation. In contrast to Δ13C, WUE showed a stronger correlation with elevation than with longitude, which increased as elevation and longitude increased. According to the carbon-oxygen model, plant stomatal conductance (gs) and photosynthetic capacity (Amax) decreased with increasing precipitation and relative humidity, while the values increased with increasing elevation and longitude. The combined analysis of carbon and oxygen isotopes of organic matters would yield additional environmental and gas exchange information for studies on climate tracing and vegetation physiology studies on the southeastern margin of the Qinghai-Tibet Plateau.

Silicate weathering linked with global climate change along the Mid-Pleistocene transition: A record from the Himalayan foreland Basin, India

Tectonic uplift and climate change play a pivotal role in controlling silicate weathering in the source region. Being adjacent to the hinterland, the sediments of the Himalayan foreland basin (HFB) hold an excellent archive to elucidate weathering link with climate and uplift. In this study, we present geochemical records of major, trace and rare earth elements, clay mineral compositions as well as the environmental magnetic and stable carbon isotope composition (δ13C) of siliciclastic sediments of the HFB over the past 2.0 Ma. These records have been used to link silicate weathering with global climate change along the Mid-Pleistocene Transition (MPT) period. The source rock compositions are characterized by selected elemental ratios, i.e., Cr/Th, Th/Sc, Th/Co and La/Sc as well as other geochemical proxies such as Al2O3/TiO2 and TiO2/Zr, suggesting a felsic source rock composition. The enriched LREE pattern of Chondrite-normalised REE with a negative Europium anomaly also attributes to felsic source rock composition. All these inferences suggest that most of the studied sediments were derived from mixed sources of the Higher Himalayan rocks and the Lesser Himalayan crystalline regions. A declining trend in kaolinite/(illite + chlorite) ratios, decreasing values of geochemical weathering indices (such as Rb/Sr and CIA), a decrease in magnetic susceptibility and gradual depleted value of δ13C indicate a decrease in chemical weathering of the siliciclastic rocks in the source region, which is most probably associated with the global climate change from warm-humid to cold-dry condition along the MPT. This suggests that variation in silicate weathering in the Himalayan region are mainly controlled by global climate and monsoon conditions.

Middle Eocene Climatic Optimum (MECO) and its imprint in the continental Escanilla Formation, Spain

Abstract. The Middle Eocene Climatic Optimum (MECO) is a global warming event mainly recognized in the marine domain and described less in the terrestrial environment. Here we present a comprehensive geochemical record of the MECO from the Escanilla Formation, a fluvial sedimentary succession in the southern Pyrenees, Spain, based on a suite of sampled paleosols, fluvial stromatolites, and pedogenic nodules. Our multiproxy approach involves using carbon and oxygen stable isotope compositions to identify the regional preservation of the MECO, calculate chemical weathering intensity and mean annual precipitation, perform clumped isotopes on carbonates, and identify clay mineralogy assemblages of paleosols. Results indicate that the Middle Eocene interval in the southern Pyrenees was characterized by low weathering rates under warm and arid climatic conditions. This is further supported by the presence of smectite, palygorskite, illite, and chlorite, which suggest seasonal rainfall but under generally dry conditions resulting in weak chemical weathering. Importantly, a negative organic carbon isotopic excursion indicates the regional, terrestrial impact of the MECO, highlighting that fluvial sedimentary successions even in active foreland basins can represent particularly interesting terrestrial archives of past changes in global climate.

Land use changes and edaphic properties control contents and isotopic compositions of soil organic carbon and nitrogen in wetlands

Land use change in wetlands leads to significant losses of soil organic matter (SOM). Stable carbon (C) and nitrogen (N) isotopes offer insights into changes in C3/C4 vegetation, SOM sources, and decomposition processes. Yet, predicting the spatial–temporal dynamics of SOM contents and isotopes under land use changes remains challenging. This study delves into the effects of land use changes on soil organic carbon (SOC), total nitrogen (TN), δ13C and δ15N values, and soil physico-chemical properties and lignin phenols. Our results highlight the significance of soil water content (SWC) in determining the outcomes of land use changes. The conversion of wetland to cropland, forestland and construction land, led to notable reductions in SOC contents (8.71–56.33 %), and TN contents (7.87–37.12 %). Wetland conversion resulted in an enrichment of 13C and 15N abundance, with wetlands exhibiting the lowest δ13C (−25.57 to –22.89 ‰) and δ15N (2.66 to 6.67 ‰) values. A significant correlation occurred between δ13C and δ15N values in wetlands, but underwent considerable changes after wetland conversion. Key parameters, including bulk density (BD), C:N, the acid-to-aldehyde of vanillyl ((Ad/Al)v), lignin content (Λ8), and total phosphorus (TP), were identified as influencing factors for both SOC and TN contents. When evaluating δ13C values, the most influential factors included silt, C:N, SOC, sand, and BD. These indicate the importance of soil chemical group (from 41 % to 21 %) in elucidating δ13C values declined, while lignin group’s (from 9 % to 28 %) importance increased from topsoil to subsoil. The acid-to-aldehyde of syringyl ((Ad/Al)s), Λ8, C:N, BD and the cinnamyl-to-vanillyl ratio (C/V) were identified as the primary factors influencing δ15N values, with chemical group accounting for 36 % and lignin group for 48 % in topsoil, while physical group dominated 42 % in subsoil. Our findings underscore the shifts in SOM sources and distinct mechanisms of degradation/preservation of SOM following land use changes.

Thermocline-level connectivity between the tropical equatorial Pacific and tropical northeast Pacific during deglaciation

The connection of the Southern Ocean and Eastern Equatorial Pacific (EEP) has been used to explain the presence of an old, respired water mass into the Eastern Tropical North Pacific (ETNP) and Eastern North Pacific (ENP) during deglaciation. This water mass and its geochemical properties are transported along the thermocline via subsurface and intermediate circulation. Some questions remain regarding an intermediate water mass with old and less ventilated characteristics in the eastern Pacific because certain sedimentary records of δ13C, δ18O, and Δ14C in benthic foraminifera have failed to prove its presence. The top-down hypothesis has been proposed to explain the absence of this carbon isotopic signal in benthic and its presence in planktonic foraminifera in the EEP. To prove this hypothesis in the ETNP, oxygen and carbon isotopic compositions were determined for Neogloboquadrina dutertrei in a core collected at 700 m depth over the Magdalena margin, Mexico. From these new data, a reconstruction of the water column structure and the change in ocean circulation at the thermocline level during deglaciation was inferred. N. dutertrei δ18O values in the ETNP and those from Globigerina bulloides in the ENP, similar to those of N. dutertrei in the EEP, suggest that the tropical water mass extended as far as 32 °N. Specifically, N. dutertrei δ18O values were more positive in the Heinrich Stadial-1 (HS-1) and Younger Dryas (YD) than the Bolling Allerod-Antarctic Cold Reversal (BA-ACR) and Early Holocene (EH) suggesting the presence of a saline water mass with origin in the EEP. N. dutertrei δ13C depleted values during the HS-1 and YD suggested the presence of a water mass with old and respired carbon. This is consistent with the salinification or “spicy” inferred from δ18O for the ETNP. These isotopic findings in N. dutertrei corroborate the existence of a tropical water mass that probably originated in the Southern Ocean. Additionally, the present data do not support the top-down hypothesis.

Geological characteristics and exploration breakthroughs of coal rock gas in Carboniferous Benxi Formation, Ordos Basin, NW China

To explore the geological characteristics and exploration potential of the Carboniferous Benxi Formation coal rock gas in the Ordos Basin, this paper presents a systematic research on the coal rock distribution, coal rock reservoirs, coal rock quality, and coal rock gas features, resources and enrichment. Coal rock gas is a high-quality resource distinct from coalbed methane, and it has unique features in terms of burial depth, gas source, reservoir, gas content, and carbon isotopic composition. The Benxi Formation coal rocks cover an area of 16×104 km², with thicknesses ranging from 2 m to 25 m, primarily consisting of bright and semi-bright coals with primitive structures and low volatile and ash contents, indicating a good coal quality. The medium-to-high rank coal rocks have the total organic carbon (TOC) content ranging from 33.49% to 86.11%, averaging 75.16%. They have a high degree of thermal evolution (Ro of 1.2%–2.8%), and a high gas-generating capacity. They also have high stable carbon isotopic values (δ13C1 of –37.6‰ to –16‰; δ13C2 of –21.7‰ to –14.3‰). Deep coal rocks develop matrix pores such as gas bubble pores, organic pores, and inorganic mineral pores, which, together with cleats and fractures, form good reservoir spaces. The coal rock reservoirs exhibit the porosity of 0.54%–10.67% (averaging 5.42%) and the permeability of (0.001–14.600)×10−3 μm2 (averaging 2.32×10−3 μm2). Vertically, there are five types of coal rock gas accumulation and dissipation combinations, among which the coal rock-mudstone gas accumulation combination and the coal rock-limestone gas accumulation combination are the most important, with good sealing conditions and high peak values of total hydrocarbon in gas logging. A model of coal rock gas accumulation has been constructed, which includes widespread distribution of medium-to-high rank coal rocks continually generating gas, matrix pores and cleats/fractures in coal rocks acting as large-scale reservoir spaces, tight cap rocks providing sealing, source-reservoir integration, and five types of efficient enrichment patterns (lateral pinchout complex, lenses, low-amplitude structures, nose-like structures, and lithologically self-sealing). According to the geological characteristics of coal rock gas, the Benxi Formation is divided into 8 plays, and the estimated coal rock gas resources with a buried depth of more than 2 000 m are more than 12.33×1012 m3. The above understandings guide the deployment of risk exploration. Two wells drilled accordingly obtained an industrial gas flow, driving the further deployment of exploratory and appraisal wells. Substantial breakthroughs have been achieved, with the possible reserves over a trillion cubic meters and the proved reserves over a hundred billion cubic meters, which is of great significance for the reserves increase and efficient development of natural gas in China.

Characteristics of carbon isotopic composition of alkane gas in large gas fields in China

Exploration and development of large gas fields is an important way for a country to rapidly develop its natural gas industry. From 1991 to 2020, China discovered 68 new large gas fields, boosting its annual gas output to 1 925×108 m3 in 2020, making it the fourth largest gas-producing country in the world. Based on 1696 molecular components and carbon isotopic composition data of alkane gas in 70 large gas fields in China, the characteristics of carbon isotopic composition of alkane gas in large gas fields in China were obtained. The lightest and average values of δ13C1, δ13C2, δ13C3 and δ13C4 become heavier with increasing carbon number, while the heaviest values of δ13C1, δ13C2, δ13C3 and δ13C4 become lighter with increasing carbon number. The δ13C1 values of large gas fields in China range from −71.2‰ to −11.4‰ (specifically, from −71.2‰ to −56.4‰ for bacterial gas, from −54.4‰ to −21.6‰ for oil-related gas, from −49.3‰ to −18.9‰ for coal-derived gas, and from −35.6‰ to −11.4‰ for abiogenic gas). Based on these data, the δ13C1 chart of large gas fields in China was plotted. Moreover, the δ13C1 values of natural gas in China range from −107.1‰ to −8.9‰, specifically, from −107.1‰ to −55.1‰ for bacterial gas, from −54.4‰ to −21.6‰ for oil-related gas, from −49.3‰ to −13.3‰ for coal-derived gas, and from −36.2‰ to −8.9‰ for abiogenic gas. Based on these data, the δ13C1 chart of natural gas in China was plotted.

Constraints on hopanes and brGDGTs as pH proxies in peat

pH is one of the major parameters governing peat functioning, and pH variations in modern peatlands affect carbon and methane production and consumption. Paleo-pH reconstructions have been limited thus far, but they could help to better understand peat functioning in variety of settings and also serve as an indirect proxy for climatic and environmental variations such as precipitation. Bacterial hopanes and branched Glycerol Dialkyl Glycerol Tetraethers (brGDGTs) were investigated in a 10-ka peat record from North-East Cameroon (NGaoundaba, Western Central Africa). Recently developed pH proxies using the hopane ββ/(αβ + ββ) ratio and the brGDGT cyclization ratio (CBTpeat) were applied and compared with previously published bulk organic data from the same core. Different hypotheses are usually proposed to explain the high abundance of the “thermally mature” C31 αβ hopane in peats: acid-catalyzed isomerization of ββ to αβ isomers with or without biological mediation or the direct input of C31 αβ hopanes by bacteria. In the NGaoundaba peat deposit, the opposite variation in the ββ/(αβ + ββ) ratio of C30 and C31 hopanes and the carbon isotopic composition of C31 ββ and αβ hopanes suggest that an eventual transformation of C31 ββ to αβ isomers is not possible without biological mediation. A linear correlation between hopane- and brGDGT-reconstructed pH is observed, suggesting a similar response to environmental changes for these two independent proxies. A large increase in reconstructed pH values coincides with changes in vegetation and precipitation at the end of the African Humid Period (AHP). Lower pH values are observed during the AHP, coinciding with a period of increased precipitation and consistent with bulk organic data and slightly higher C31 ββ hopane δ13C values compared to middle and late Holocene. Bulk organic data indicate an interruption of the AHP by a drier intermission that coincides with a decrease in reconstructed pH values, probably reflecting a decrease in evapotranspiration. Variations in pH values could be interpreted in terms of preservation of peat organic matter and might reflect past changes in methane cycling in the investigated peatland. The present study reinforces the idea that reconstruction of pH in peat deposits represents a promising proxy of environmental change, enabling a better understanding of changes in peat functioning over large timescales and various locations.

Using Multi‐Homolog Plant‐Wax Carbon Isotope Compositions to Reconstruct Tropical Vegetation Types

AbstractThe stable carbon isotope composition (δ13C) of plant components such as plant wax biomarkers is an important tool for reconstructing past vegetation. Plant wax δ13C is mainly controlled by photosynthetic pathways, allowing for the differentiation of C4 tropical grasses and C3 forests. Proxy interpretations are however complicated by additional factors such as aridity, vegetation density, elevation, and the considerable δ13C variability found among C3 plant species. Moreover, studies on plant wax δ13C in tropical soils and plants have focused on Africa, while structurally different South American savannas, shrublands and rainforests remain understudied. Here, we analyze the δ13C composition of long‐chain n‐alkanes and fatty acids from tropical South American soils and leaf litter to assess the isotopic variability in each vegetation type and to investigate the influence of climatic features on δ13C. Rainforests and open vegetation types show distinct values, with rainforests having a narrow range of low δ13C values (n‐C29 alkane: ‰ ; Suess‐effect corrected). This allows for the detection of even minor incursions of savanna (δ13C n‐C29 alkane ‰) into rainforests. While Cerrado savannas and semi‐arid Caatinga shrublands grow under distinctly different climates, they can yield indistinct δ13C values for most compounds. Cerrado soils and litter show pronounced isotopic spreads between the n‐C33 and n‐C29 alkanes, while Caatinga shrublands show consistent values across the two homologs, thereby enabling the differentiation of these vegetation types. The same multi‐homolog isotope analysis can be extended to differentiate African shrublands from savannas.

Multiple enrichment mechanisms of organic matter in the Fengcheng Formation of Mahu Sag, Junggar Basin, NW China

Based on core and thin section data, the source rock samples from the Fengcheng Formation in the Mahu Sag of the Junggar Basin were analyzed in terms of zircon SIMS U-Pb geochronology, organic carbon isotopic composition, major and trace element contents, as well as petrology. Two zircon U-Pb ages of (306.0±5.2) Ma and (303.5±3.7) Ma were obtained from the first member of the Fengcheng Formation. Combined with carbon isotopic stratigraphy, it is inferred that the depositional age of the Fengcheng Formation is about 297–306 Ma, spanning the Carboniferous–Permian boundary and corresponding to the interglacial period between C4 and P1 glacial events. Multiple increases in Hg/TOC ratios and altered volcanic ash were found in the shale rocks of the Fengcheng Formation, indicating that multiple phases of volcanic activity occurred during its deposition. An interval with a high B/Ga ratio was found in the middle of the second member of the Fengcheng Formation, associated with the occurrence of evaporite minerals and reedmergnerite, indicating that the high salinity of the water mass was related to hydrothermal activity. Comprehensive analysis suggests that the warm and humid climate during the deposition of Fengcheng Formation is conducive to the growth of organic matter such as algae and bacteria in the lake, and accelerates the continental weathering, driving the input of nutrients. Volcanic activities supply a large amount of nutrients and stimulate primary productivity. The warm climate and high salinity are conducive to water stratification, leading to water anoxia that benefits organic matter preservation. The above factors interact and jointly control the enrichment of organic matter in the Fengcheng Formation of Mahu Sag.

Tracing of natural gas migration by light hydrocarbons: A case study of the Dongsheng gas field in the Ordos Basin, NW China

Based on the analysis of light hydrocarbon compositions of natural gas and regional comparison in combination with the chemical components and carbon isotopic compositions of methane, the indication of geochemical characteristics of light hydrocarbons on the migration features, dissolution and escape of natural gas from the Dongsheng gas field in the Ordos Basin is revealed, and the effect of migration on specific light hydrocarbon indexes is further discussed. The study indicates that, natural gas from the Lower Shihezi Formation (P1x) in the Dongsheng gas field displays higher iso-C5−7 contents than n-C5−7 contents, and the C6−7 light hydrocarbons are composed of paraffins with extremely low aromatic contents (<0.4%), whereas the C7 light hydrocarbons are dominated by methylcyclohexane, suggesting the characteristics of coal-derived gas with the influence by secondary alterations such as dissolution. The natural gas from the Dongsheng gas field has experienced free-phase migration from south to north and different degrees of dissolution after charging, and the gas in the Shiguhao area to the north of the Borjianghaizi fault has experienced apparent diffusion loss after accumulation. Long-distance migration in free phase results in the decrease of the relative contents of the methylcyclohexane in C7 light hydrocarbons and the toluene/n-heptane ratio, as well as the increase of the n-heptane/methylcyclohexane ratio and heptane values. The dissolution causes the increase of isoheptane values of the light hydrocarbons, whereas the diffusion loss of natural gas in the Shiguhao area results in the increase of n-C5−7 contents compared to the iso-C5−7 contents.