Petroleum source rocks of the Tarfaya Basin and adjacent areas, Morocco

This work characterizes the source rock potential of the Tarfaya Basin and enabled us to reconstruct its geochemical history. Outcrop samples covering different stratigraphic intervals, plus the northwestern part of the Zag/Tindouf Basin (Bas Draa area), were analyzed for total organic carbon (C_org) and total inorganic carbon contents and total sulfur content. Rock-Eval analysis and vitrinite reflectance measurements were performed on 56 samples chosen on the basis C_org content. A set of 45 samples were extracted and non-aromatic hydrocarbons were analyzed by way of gas chromatography-flame ionization detection (GC-FID) and GC-mass spectrometry (GC-MS). Non-isothermal open system pyrolysis at different heating rates was applied to obtain kinetic parameters for modelling petroleum generation from four different source rocks.High quality petroleum source rocks with high C_org content and hydrogen index (HI) values were found for samples of Eocene, Coniacian, Turonian and Cenomanian age. Most samples were carbonate rich and organic/sulfur values were high to moderate. Various maturity parameters indicated immature or possibly early mature organic matter. Based on organic geochemical and petrological data, the organic matter is of marine/aquatic origin (Cenomanian) or a mixture of aquatic and terrigenous material (Eocene). The Early Cretaceous interval did not contain high quality source rocks, but indications of petroleum impregnation were found.     

Soil quality changes in land degradation as indicated by soil chemical, biochemical and microbiological properties in a karst area of southwest Guizhou, China

Not only the nutritional status and biological activity but also the soil ecological functioning or soil health has been impacted profoundly by land degradation in the karst area of southwest China where the karst ecosystems are generally considered as extremely vulnerable to land degradation under intensified land-use changes. The objectives of this study are to elucidate the changes in overall soil quality by a holistic approach of soil nutritional, biological activity, and soil health indicators in the karst area as impacted by intense cultivation and vegetation degradation. Topsoil samples were collected on selected eco-tesserae in a sequence of land degradation in a karst area of southwest Guizhou in 2004. The soil nutrient pools of organic carbon (C_org), extractable extracellular carbon (C_ext), total soil nitrogen (N_t), alkali-hydrolyzable nitrogen (N_ah), total phosphorus (P_t), available phosphorus (P_a) were analyzed by wet soil chemistry. The soil biological properties were studied by means of measurements of microbial biomass carbon (both by fumigation–extraction, FE-C_mic, and by calculation from substrate-incubation respiration, SIR-C_mic) of respiration [respiration without addition of substrates, basal respiration (BR), and potential respiration (PR) with substrate-incubation] and of soil enzyme activities (invertase, urease, and alkaline phosphatase). Soil health status was assessed by simple indices of C_mic/C_org and BR/C_mic in conjunction with bacterial community structures determined by polymerase chain reaction and denaturing gradient gel electrophoresis. While the nutritional pool parameters, such as C_org and C_ext, described basically the changes in soil life-supporting capacity with cultivation interference and vegetation declined, those parameters of biological activity such as FE-C_mic, SIR, and SIR-C_mic as well as bacterial community structures measured by molecular method evidenced well the changes in soil functioning for ecosystem health with the land degradation.     

Organic fraction of the total carbon burial flux deduced from carbon isotopes across the Permo-Triassic boundary at Meishan,Zhejiang Province,China

By combining the carbon cycle model with the records of carbonate and organic (kerogen) carbon isotope, this paper presents the calculation of the fraction of organic carbon burial (f _org) of beds 23–40 at the global boundary stratotype section and point (GSSP) of the Permian-Triassic boundary at Meishan, Zhejiang Province. The resulting calculation produces two episodes of f _org maxima observed to occur at beds 23–24 and 27–29, which respectively corresponds to the two episodic anoxic events indicated by the flourish of green sulfur bacteria. Two episodic f _org minima occurred at beds 25–26 and 32–34, generally coincident with the flourish of cyanobacteria (bed 26 and upper part of beds 29 to 34) as shown by the high value of 2-melthyhopnoanes. It appears that the f _org is related to the redox conditions, with greater f _org values observed under the reductive condition. The relationship between f _org and the total organic carbon (TOC) content was complex. The f _org value was low at some beds with a high TOC content (such as bed 26), while high observed at some beds with a low TOC content (e.g. bed 27). This association infers the important contribution of primary productivity to the TOC content. The original organic burial could be thus calculated through the configuration of the function of the primary productivity and f _org, which can be used to correct the residual TOC measured today. This investigation indicates that compiling the organic-inorganic carbon isotopes with the carbon cycle model favors to understand the fraction of organic carbon burial, providing information for the reconstruction of the coupling among biota, environments and organic burial. Journal of China University of Geosciences, 2007, 32(6): 767–773 [译自: 地球科学—中国地质大学学报]     

Identical carbon isotope trends of carbonate and organic carbon and their environmental significance from the Changhsingian (end-Permian), Meishan,South China

High resolution carbon isotope analyses of carbonate and organic carbon from Meishan, South China showed that the variation of δ13Ccarb is marked by three large positive excursions during the Changhsingian (end-Permian). Carbon isotope stratigraphy during this stage shows three cyclic intervals in δ13Ccarb, with two cycles corresponding to the lower (Paleofusulinid minima Zone) and one corresponding to the upper Changhsingian (P. sinensis Zone). The large positive δ13Ccarb excursions indicate episodes of enhanced burial of isotopically light or-ganic carbon, presumably in response to deep-water anoxia episodically extending into shallow water with the rise of sea level. The organic carbon during the Changhsingian is distinguished into two groups, and the δ13Corg of each group parallels (separately) the more detailed profile of δ13Ccarb, strongly showing that the values of fractionation Δ13Ccab-org remain relatively constant, with only two intervals with anomaly. The enhanced fractionation Δ13Ccab-org with large negative δ13Corg excursions apparently indicates significant inputs from sulfide-oxidizing bacteria and green sulfur bacteria, notably at bed 24 just predating mass extinction. Our evidence appears to support that the ex-tended euxinic water is possible for the main pulse of mass extinction at the end-Permian.     

C-S-Fe relationships and the isotopic composition of pyrite in the New Albany Shale of the Illinois Basin,U.S.A.

The relationship between pyritic sulfur content (S_pyr) and organic carbon content (C_org) of shales analyzed from the New Albany Group depends upon C_org. For samples of <6 wt.% C_org, S_pyt, and C_org are strongly correlated (r = 0.85). For C_org-“rich” shales (>6 wt.%), no S_pty-C_org, correlation is apparent. The degree of Fe pyritization (DOP) shows similar relationships to C_org. These C-S-Fe relationships suggest that pyrite formation was limited by the availability of metabolizable organic carbon in samples where C_org < 6 wt.% and by the availability of reactive Fe for samples where C_org > 6 wt.%. Apparent sulfur isotope fractionations relative to contemporaneous seawater sulfate (Δ³⁴S) for pyrite formation average −40% for non-calcareous shales and −25%. for calcareous shales. Δ³⁴S values become smaller with increasing C_org, S_pyt, and DOP for all C_org-“poar” (<6 wt%) and some C_org-“nch” (<6 wt.%) shales. These trends suggest that pyrite formation occurred in a closed system or that instantaneous bacterial fractionation for sulfate reduction decreased in magnitude with increasing organic carbon content. The isotopic trends observed in the New Albany Group are not necessarily representative of other shales having a comparable range of organic carbon content, e.g. Cretaceous shales and mudstones from the western interior of North America (GAUTIER, 1986). Δ³⁴S values in the remainder of the C_org-rich New Albany Group shales are relatively large (−38 to −47%.) and independent of C_org, S_pyr, and DOP, which suggests that pyrite in these shales formed mostly at or above the sediment-water interface by precipitation from an isotopically uniform reservoir of dissolved H₂S.     

The Determination of Total Hydrogen, Carbon, Nitrogen and Sulfur in Silicates, Silicate Rocks, Soils and Sediments

Determinations of the volatile elements carbon, hydrogen, sulfur and nitrogen in many geological RM, performed with the LECO CHN and SC analysers, are presented. The method allowed the determination of S in concentrations from a few % m/m to 0.001% m/m or less, of C from % m/m to 0.01% m/m and of H from % m/m to 0.004% m/m. Accuracy was usually better than the XRF method (for S). All obtained values passed the Sutarno-Steger test, which establishes that |(mean_analysed - mean_certified)|/ S_certified < 2, for the cases with an appropriate number of determinations (n > 10 for each element). It was possible to perform routine determination of C, H and S with the instrumentation, coupled with the determination of major and minor elements in geological materials. Determination of nitrogen could also be performed on an exploratory basis, with improvements in the method dependent on the future availability of more reference materials with reliable composition of this element.     

A Lateglacial and Holocene organic carbon isotope record of lacustrine palaeoproductivity and climatic change derived from varved lake sediments of Lake Holzmaar,Germany

A composite varve-dated 11.4 m long sediment sequence from Lake Holzmaar, situated in the Eifel region of western Germany, was investigated for total organic matter content, total nitrogen content and stable organic carbon isotopes. Mean time resolution is 75 years for TN and 14 years for δ¹³C_org. On millennial time scales primary production of lacustrine algae strongly depends on the delivery of nutrients from the catchment. The respective carbon isotope record is characterized by marked variations of δ¹³C_org ranging from −36.0‰ to −27.0‰ and includes a number of pronounced shifts. Reactions of the lacustrine system and the catchment to changes of environmental parameters, e.g. runoff, solar radiation and temperature, induce changes of algal associations and of lacustrine primary production which are reflected in the sediments as carbon isotope variations. Clear evidence of ecosystem reorganizations is detected by the carbon isotope record around 14,200, 10,400, 9600, 5500, 2700, 1700 and 900 varve years BP. In particular, the Holocene events of 9600, around 5500 and 2700 are interpreted as the expression of massive changes of the climate system. The steady rise of δ¹³C_org values during the mid-Holocene is interpreted as a continuous climatic amelioration reaching an optimum around 6500 varve years BP. Rapid and large changes of δ¹³C_org values from 2700 varve years BP to the present indicate major disturbances in the catchment area. These are most probably related to deforestation or reforestation and runoff changes, presumably in conjunction with human impact. Carbon isotopes, thus, characterize the Holzmaar ecosystem in time revealing lacustrine palaeoproductivity as well as providing palaeoenvironmental and palaeoclimatic information.     

Paired δ13Ccarb and δ13Corg records of the Ordovician on the Yangtze platform,South China

During the Ordovician, huge biological revolutions and environmental changes happened in Earth’s history, including the Great Ordovician Biodiversification Event, global cooling and so on, but the cause of these events remains controversial. Herein, we conducted a paired carbon isotopic analysis of carbonate (δ¹³C_carb) and organic matter (δ¹³C_org) through the Ordovician in the Qiliao section on the Yangtze platform of South China. Our results showed that the δ¹³C_carb trend of the Qiliao section can be correlated with local and global curves. The δ¹³C_org trend seems is less clear than the δ¹³C_carb trend for stratigraphic correlations, but some δ¹³C_org positive excursions in the Middle and Upper Ordovician may be used for correlation studies. These carbon isotopic records may have global significance rather than local significance, revealing several fluctuations to the global carbon cycle during the Ordovician. Several known δ¹³C_carb and δ¹³C_org negative and positive excursions have been recognised in this study, including the early Floian Negative Inorganic Carbon (δ¹³C_carb) Excursion (EFNICE), as well as the early Floian Positive Organic Carbon (δ¹³C_carb) Excursion, the mid-Darriwilian Inorganic Carbon (δ¹³C_carb and δ¹³C_org) Excursion (MDICE), and the early Katian Guttenberg Inorganic Carbon (δ¹³C_carb and δ¹³C_org) Excursion (GICE). These positive excursions and a smooth decline trend of δ¹³C_org values during the early to mid-Floian may imply multiple episodes of enhanced organic carbon burial that began at the early Floian stage, probably resulting in further decline in atmospheric pCO₂ and then global cooling.     

Atmospheric weathering of Scandinavian alum shales and the fractionation of C,N and S isotopes

Subaerial exposure and oxidation of organic carbon (C_org)-rich rocks is believed to be a key mechanism for the recycling of buried C and S back to Earth's surface. Importantly, processes coupled to microbial C_org oxidation are expected to shift new biomass δ¹³C_org composition towards more negative values relative to source. However, there is scarcity of information directly relating rock chemistry to oxidative weathering and shifting δ¹³C_org at the rock-atmosphere interface. This is particularly pertinent to the sulfidic, C_org-rich alum shale units of the Baltoscandian Basin believed to constitute a strong source of metal contaminants to the natural environment, following subaerial exposure and weathering. Consistent with independent support, we show that atmospheric oxidation of the sulfidic, C_org-rich alum shale sequence of the Cambrian-Devonian Baltoscandian Basin induces intense acid rock drainage at the expense of progressive oxidation of Fe sulfides. Sulfide oxidation takes priority over microbial organic matter decomposition, enabling quantitative massive erosion of C_org without producing a δ¹³C shift between acid rock drainage precipitates and shale. Moreover, ¹³C enrichment in inorganic carbon of precipitates does not support microbial C_org oxidation as the predominant mechanism of rock weathering upon exposure. Instead, a Δ³⁴S = δ³⁴S_shale − δ³⁴S_precipitates ≈ 0, accompanied by elevated S levels and the ubiquitous deposition of acid rock drainage sulfate minerals in deposited efflorescent precipitates relative to shales, provide strong evidence for quantitative mass oxidation of shale sulfide minerals as the source of acidity for chemical weathering. Slight δ¹⁵N depletion in the new surface precipitates relative to shale, coincides with dramatic loss of N from shales. Collectively, the results point to pyrite oxidation as a major driver of alum black shale weathering at the rock-atmosphere interface, indicating that quantitative mass release of C_org, N, S, and key metals to the environment is a response to intense sulfide oxidation. Consequently, large-scale acidic weathering of the sulfide-rich alum shale units is suggested to influence the fate and redistribution of the isotopes of C, N, and S from shale to the immediate environment.     

The effects of surface area, grain size and mineralogy on organic matter sedimentation and preservation across the modern Squamish Delta, British Columbia: the potential role of sediment surface area in the formation of petroleum source rocks

Surface sediment samples were collected from the Squamish River Delta, British Columbia, in order to determine the role of sediment surface area in the preservation of organic matter (OM) in a paralic sedimentary environment. The Squamish Delta is an actively prograding delta, located at the head of Howe Sound.Bulk total organic carbon (TOC) values across the Squamish Delta are low, ranging from 0.1 to 1.0 wt.%. The carbon/total nitrogen ratio (C_org/N) ranges from 6 to 17, which is attributed to changes in OM type and facies variations. The <25-μm fraction has TOC concentrations up to 2.0 wt.%, and a C_org/N ratio that ranges from 14 to 16. The 53–106-μm fraction has higher TOC concentrations and C_org/N ratios relative to the 25–53-μm fraction. The C_org/N ratio ranges from 9 to 18 in the 53–106-μm fraction and 5.5–10.5 in the 25–53-μm fraction. Surface area values for bulk sediments are low (0.5–3.0 m²/g) due to the large proportion of silt size material. Good correlation between surface area and TOC in bulk samples suggests that OM is adsorbed to mineral surfaces. Similar relationships between surface area and TOC were observed in size-fractionated samples. Mineralogy and elemental composition did not correlate with TOC concentration.The relationships between surface area, TOC and total nitrogen (TN) can be linked to the hydrodynamic and sedimentological conditions of the Squamish Delta. As a result, the Squamish Delta is a useful modern analogue for the formation of petroleum source rocks in ancient deltaic environments, where TOC concentrations are often significantly lower than those in source rocks formed in other geological settings.     

Organic nitrogen chemistry during low-grade metamorphism

Most of the organic nitrogen (N_org) on Earth is disseminated in crustal sediments and rocks in the form of fossil nitrogen-containing organic matter. The chemical speciation of fossil N_org within the overall molecular structure of organic matter changes with time and heating during burial. Progressive thermal evolution of organic matter involves phases of enhanced elimination of N_org and ultimately produces graphite containing only traces of nitrogen. Long-term chemical and thermal instability makes the chemical speciation of N_org a valuable tracer to constrain the history of sub-surface metamorphism and to shed light on the subsurface biogeochemical nitrogen cycle and its participating organic and inorganic nitrogen pools. This study documents the evolutionary path of N_org speciation, transformation and elimination before and during metamorphism and advocates the use of X-ray photoelectron spectroscopy (XPS) to monitor changes in N_org speciation as a diagnostic tool for organic metamorphism. Our multidisciplinary evidence from XPS, stable isotopes, traditional quantitative coal analyses, and other analytical approaches shows that at the metamorphic onset N_org is dominantly present as pyrrolic and pyridinic nitrogen. The relative abundance of nitrogen substituting for carbon in condensed, partially aromatic systems (where N is covalently bonded to three C atoms) increases exponentially with increasing metamorphic grade, at the expense of pyridinic and pyrrolic nitrogen. At the same time, much N_org is eliminated without significant nitrogen isotope fractionation. The apparent absence of Rayleigh-type nitrogen isotopic fractionation suggests that direct thermal loss of nitrogen from an organic matrix does not serve as a major pathway for N_org elimination. Instead, we propose that hot H, O-containing fluids or some of their components gradually penetrate into the carbonaceous matrix and eliminate N_org along a progressing reaction front, without causing nitrogen isotope fractionation in the residual N_org in the unreacted core of the carbonaceous matrix. Before the reaction front can reach the core, an increasing part of core N_org chemically stabilizes in the form of nitrogen atoms substituting for carbon in condensed, partially aromatic systems forming graphite-like structural domains with delocalized π-electron systems (nitrogen atoms substituting for “graphitic” carbon in natural metamorphic organic matter). Thus, this nitrogen species with a conservative isotopic composition is the dominant form of residual nitrogen at higher metamorphic grade.     

Seagrass Organic Carbon Stocks Show Minimal Variation Over Short Time Scales in a Heterogeneous Subtropical Seascape

Blue carbon initiatives require accurate monitoring of carbon stocks. We examined sources of variability in seagrass organic carbon (C_org) stocks, contrasting spatial with short temporal scales. Seagrass morphology and sediment C_org stocks were measured from biomass and shallow sediment cores collected in Moreton Bay, Australia. Samples were collected between 2012 and 2013, from a total of 77 sites that spanned a gradient of water turbidity. Environmental measures of water quality between 2000 and 2013 revealed strong seasonal fluctuations from summer to winter, yet seagrass biomass exhibited no temporal variation. There was no temporal variability in C_org stocks, other than below ground biomass stocks were slightly higher in June 2013. Seagrass locations were grouped into riverine, coastal, and seagrass loss locations and short temporal variability of C_org stocks was analysed within these categories to provide clearer insights into temporal patterns. Above ground C_org stocks were similar between coastal and riverine meadows. Below ground C_org stocks were highest in coastal meadows, followed by riverine meadows. Sediment C_org stocks within riverine meadows were much higher than at coastal meadows and areas of seagrass loss, with no difference in sediment C_org stocks between these last two categories. Riverine seagrass meadows, of higher turbidity, had greater total C_org stocks than meadows in offshore areas irrespective of time. We suggest that C_org stock assessment should prioritise sampling over spatial gradients, but repeated monitoring over short time scales is less likely to be warranted if environmental conditions remain stable.     

新疆罗北洼地湖相沉积物有机碳同位素的变化序列及其古环境意义

测定了新疆罗布泊地区湖相沉积物CK-2钻孔样品的总有机碳含量（TOC）及其同位素组成、碳酸盐含量和C/N比值等环境代用指标,以及石膏矿物的质谱-铀系年龄。测试结果表明,20～9kaB.P.期间沉积物δ¹³C_org.在-23.4‰～-16.1‰之间波动且阶段性明显,与TOC呈现良好的相关关系,整体变化趋势同南极Dome C冰芯中记录的全球大气CO₂浓度一致;C/N比值表明有机碳来源主要是陆生高等植物。因此大气CO₂浓度变化是影响20～9kaB.P.期间罗布泊湖相沉积物δ¹³C_org.值变化的主导因素,周围山体上C₃/C₄植物相对生物量的变化则是另一重要因素。依据δ¹³C_org.的变化序列将此时间段湖区古环境的演化分成6个阶段:20.0～14.1kaB.P.期间受到末次盛冰期的影响,气温偏低,湖水丰沛;14.1～13.3kaB.P.是一个气候不稳定期,冷暖波动较频繁,但以暖为趋势;13.3～12.8kaB.P.期间经历了一段冷期,于12.8kaB.P.结束了末次冰期,随后气候开始转暖至11.8kaB.P.;其后气温再次变冷并维持到10kaB.P.;最后从10kaB.P.进入全新世暖期。δ¹³C_org.序列明显向偏负方向变化,表明该地区变暖的趋势相当明显。罗布泊地区日益干旱化是全球气候变化的结果,尤其是受到全球CO₂浓度的不断升高所制约。     

Organic Carbon Isotope Geochemistry of the Neoproterozoic Doushantuo Formation, South China

The Neoproterozoic Doushantuo Formation on the Yangtze Platform, South China, documents a sedimentary succession with different sedimentary facies from carbonate platform to slope and to deep sea basin, and hosts one of the world-class phosphorite deposits. In these strata, exquisitely preserved fossils have been discovered： the Weng＇an biota. This study presents carbon isotope geochemistry which is associated paired carbonate and organic matter from the Weng＇an section of a carbonate platform （shelf of the Yangtze Platform, Guizhou Province） from the Songtao section and Nanming section of a transition belt （slope of the Yangtze Platform, Guizhou Province） and from the Yanwutan section （basin area of the Yangtze Platform, Hunan Province）. Environmental variations and bio-events on the Yangtze Platform during the Late Neoproterozoic and their causal relationship are discussed. Negative carbon isotope values for carbonate and organic carbon （mean δ^13Corg = -35.0‰） from the uppermost Nantuo Formation are followed by an overall increase in δ^13C up-section. Carbon isotope values vary between -9.9‰ and 3.6‰ for carbonate and between -35.6‰ and -21.5‰ for organic carbon, respectively. Heavier δ^13Ccarb values suggest an increase in organic carbon burial, possibly related to increasing productivity （such as the Weng＇an biota）. The δ^13C values of the sediments from the Doushantuo Formation decreased from the platform via the slope to basin, reflecting a reduced environment with minor dissolved inorganic carbon possibly due to a lower primary productivity. It is deduced that the classical upwelling process, the stratification structure and the hydrothermal eruption are principally important mechanisms to interpret the carbon isotopic compositions of the sediments from the Doushantuo Formation.     

Assessment of the pseudo total metal content in alluvial sediments from Danube River,Serbia

We used elemental carbon, nitrogen, hydrogen and sulfur as well as ratios of hydrogen and nitrogen with total organic carbon for investigation of source and conditions of organic matter in alluvial Danube sediments. We also determined the pseudo total concentrations of metals presented as a sum of extracted concentration after five sequential extraction steps. The pseudo total metal concentrations were found to be (mg kg⁻¹) for Mn, 666; Fe, 25,852; Mg, 16,193; K, 2,063; Ni, 32.4; Zn, 72.2; Pb, 15.0; Cu, 26.0 and for Cr, 15.9. Correlation analysis and two multivariate analysis methods (principal component and cluster analysis) were helpful in determining the associations between the pseudo total extracted fractions of metals and with elemental carbon, hydrogen, nitrogen, sulfur, total inorganic and organic carbon. These correlations will help us to identify substrates of trace metals in different oxic/anoxic conditions. The correlation results of the trace metals and Fe, K, Mg and Mn suggest their adsorption, mainly onto Fe and Mn (hydro)oxides and K alumosilicates, whereas correlations of metals with sulfur indicate that they were precipitated as Fe-sulfides.     

Variation and paleoclimatic significance of organic carbon isotopes of Ili loess in arid Central Asia

As an indicator for terrestrial paleovegetation, the stable isotopic composition of total organic matter (δ¹³C_org) in loess sediments has been widely used for paleoclimatic reconstruction in western Europe, the Great Plains of North America and the Chinese Loess Plateau (CLP). However, little is known about the variation and paleoclimatic significance of the loess δ¹³C_org in arid Central Asia (ACA). We report δ¹³C_org data from an Axike (AXK) loess/paleosol profile from the eastern Ili Basin, eastern Central Asia. Along the profile, the δ¹³C_org values were more negative in the paleosol layers observed in the field and were confirmed by environmental magnetic proxies and a higher concentration of total organic carbon (TOC), consistent with results for western Europe and the northwestern CLP. Our results demonstrate that the loess δ¹³C_org in this region documents mainly the response of δ¹³C of locally predominant C₃ plants to paleoclimatic variation, especially paleoprecipitation. Our results also suggest that the loess δ¹³C_org values in the area have the potential for quantitative paleoprecipitation reconstruction on the basis of detailed δ¹³C_org results from modern plants and surface soils in the future.     

Studies on gas biogeochemistry in the near-bottom environment of aquatic areas

An integrated methodology developed by the authors for studies on marine gas biogeochemistry was used. The new data are presented for a wide variety of gas biogeochemical parameters measured synchronously in the near-bottom environment (in water and sediments). As the background, abnormally high values were found for gaseous components (hydrocarbons, helium, hydrogen, carbon dioxide, permanent gases) and for biochemical parameters (adenosine triphosphate (ATP), biomass of active living microorganisms by ATP (ALMB), various enzymatic activities, dissolved organic carbon (C_org), carbamide nitrogen, etc.). The new data set obtained allowed us to discover the effect of chemolite autotrophy in local near-bottom ecosystems. The appearance of chemolite autotrophy in the upper layer of sediment points to the occurrence of this effect in deeper layers of the sediment mass as well, as a result of deep gas fluxes. It is shown that the effect of chemolite autotrophy must be taken into account in estimating the oil and gas resources, especially in view of their continual replenishment.     

Masses of carbon in the Earth’s hydrosphere

Recent data were summarized on the concentration and mass of inorganic and organic carbon in reservoirs of the Earth’s hydrosphere. We compared carbon masses and accumulation conditions in the surface hydrosphere and waters of the sedimentary shell and proportions between carbonate, dissolved, and suspended particulate organic carbon. It was shown that the total masses of carbon in the surface hydrosphere and in the waters of the sedimentary shell are approximately equal to 80 × 10¹⁸ g C at an organic to carbonate carbon ratio of 1 : 36 and 1 : 43, respectively. Three main forms of organic compounds in the ocean (living organisms, suspended particles, and dissolved species) occur in the proportion 1 : 13 : 250 and form the pyramid of masses 4 × 10¹⁵ g, 50 × 10¹⁵ g, and 1000 × 10¹⁵ g C_org. The descending sequence of the organic to carbonate carbon ratio in water, ocean (1 : 36) > glaciers (1 : 8) > lakes (1 : 2) > rivers (1 : 0.6) > wetlands (1 : 0.3), is in general consistent with an increase in the same direction in the mean concentrations of organic matter: 0.77 mg C_org/L in the ocean, 0.7 mg C_org/L in glaciers, 6–30 mg C_org/L in lakes, 15 mg C_org/L in rivers, and 75 mg C_org/L in wetlands. Both the mean concentrations and masses of dissolved organic matter in the pore waters of oceanic sediments and in the waters of the sedimentary shell are similar: 36–37 mg/L and 5 × 10¹⁸ and 5.6 × 10¹⁸ g, respectively. The mass of carbonate carbon in the pore waters of the ocean, (19–33) × 10¹⁸ g, is comparable with its mass in the water column, 38.1 × 10¹⁸ g.     

Paleoceanographic Indicators for Early Cambrian Black Shales from the Yangtze Platform,South China: Evidence from Biomarkers and Carbon Isotopes

The lower Cambrian Niutitang Formation, a widespread black shale deposition, is of geological interest because of its polymetallic beds, Cambrian explosion, depositional ages, dramatic environmental changes and so on. Previous study focused mainly on inorganic geochemistry and few studies have investigated the organic fractions of upper Neoproterozoic-lower Cambrian strata in South China. Here we report a study of biomarkers plus organic carbon isotopes for black shales from Ganziping, Hunan Province (China). All the saturated hydrocarbon fractions have a unimodal distribution of n-alkanes, a high content of short-chain alkanes and maximize at C 19 or C 20 (C 23 for sample Gzh00-1). The C 27 /C 29 sterane ratio ranges from 0.77 to 1.20 and 4-methylsteranes are in low abundance. These parameters indicate that algae and bacteria are the important primary producers. Furthermore, biomarker maturity proxies show the samples to be higher maturity. The low Pr/Ph values (<0.7) suggest that the samples were deposited under anoxic conditions and, likely, under stratified water columns. In addition, 25-norhopanes and gammacerane are present as diagnostic indicators of normal marine salinity and dysoxic to anoxic conditions. During the Early Tommotian, known to coincide with a transgression event, small shelly fossils increased in abundance and diversity. Moreover, positive δ 13 C org excursions close to 1.4‰ occur at the base of the Tommotian stage. In summary, the Early Cambrian black shales were deposited under dramatic paleoenvironmental changes, including oceanic anoxia, higher primary productivity and sea-level rise.     

Organic Carbon versus Major Elements Relationship in Rocks of the Bazhenov Formation,Western Siberia

A close relation of the organic carbon (C_org) content with major has been established for rocks of the Upper Jurassic–Lower Cretaceous Bazhenov Formation. Applying the method of multiple linear regression, it has been demonstrated that the C_orgcontent in rocks of the Bazhenov Formation is stringently controlled by its bulk chemical composition. This inference is consistent with the existing ideas regarding a close interrelation between the following main components of rocks: organic carbon and authigenic quartz formed on remains of Radiolaria; pyrite formed in a highly reducing medium of C_org-rich sediments; and terrigenous clayey material diluting the authigenic siliceous–carbonaceous–pyritic matrix. These components chiefly determine the spectrum of major elements in the Bazhenov Formation. The establishment of the close relation between the C_orgcontent and the group of major elements refutes the suggestion of some authors that siliceous material was supplied to nonlithified sediments of the Bazhenov sea by hydrothermal solutions, because this mechanism would have inevitably upset geochemical relations between elements in the studied rocks.