江苏金湖凹陷古近系奇碳优势和偶碳优势共存的正构烷烃

苏北盆地金湖凹陷古近纪阜宁组二段暗色泥岩及其生成的原油中,正构烷烃系列存在着偶碳优势、奇碳优势以及二者共存的3种分布型式。本文重点探讨正构烷烃奇碳优势和偶碳优势共存的形成原因。在这类暗色泥岩与原油中,正构烷烃通常低碳数部分呈nC15、nC17优势,中碳数具有nC20、nC22优势,高碳数为nC25、nC27、nC29、nC31优势;并且具有强烈的植烷优势、较高的伽玛蜡烷指数、含有一定量β胡萝卜烷和C24四环萜烷。分析认为沉积水体环境和有机质来源的变化决定了正构烷烃的分布形式,该类正构烷烃形成于湖盆水体盐度分层的沉积环境,主要来源于湖盆内藻类和湖盆外高等植物蜡。      

Biogenic Volatile Organic Compounds (VOC): An Overview on Emission, Physiology and Ecology

This overview compiles the actual knowledge of the biogenic emissions of some volatile organic compounds (VOCs), i.e., isoprene, terpenes, alkanes, alkenes, alcohols, esters, carbonyls, and acids. We discuss VOC biosynthesis, emission inventories, relations between emission and plant physiology as well as temperature and radiation, and ecophysiological functions. For isoprene and monoterpenes, an extended summary of standard emission factors, with data related to the plant genus and species, is included. The data compilation shows that we have quite a substantial knowledge of the emission of isoprene and monoterpenes, including emission rates, emission regulation, and biosynthesis. The situation is worse in the case of numerous other compounds (other VOCs or OVOCs) being emitted by the biosphere. This is reflected in the insufficient knowledge of emission rates and biological functions. Except for the terpenoids, only a limited number of studies of OVOCs are available; data are summarized for alkanes, alkenes, carbonyls, alcohols, acids, and esters. In addition to closing these gaps of knowledge, one of the major objectives for future VOC research is improving our knowledge of the fate of organic carbon in the atmosphere, ending up in oxidation products and/or as aerosol particles.     

Normal Alkane Distributions in Soil Samples along a Lhasa-Bharatpur Transect

We present n-alkane distributions in the soil samples along a transect from Lhasa on the Tibetan Plateau to Bharatpur in Nepal, which covers a large geographical area and a wide range of climatic conditions. These data allow us to assess the significance of n-alkane distributions in different vegetation types and their relationships to temperature and precipitation. In the tropical rainforest and broadleaved forest zones, n-alkanes exhibit a bimodal distribution pattern with dominant homologues around n-C_(31) and n-C_(23). The bimodal distribution of tropical rainforest n-alkanes may be a general pattern because of the presence of many lianas, epiphytic plants, algae and the strong microbial activity and degradation involved in the postdepositional process. In the warm-temperate mixed forest and needle-leaved forest zones, the long-chain alkanes have a pattern of n-C_(31) n-C_(33) n-C_(27). In the alpine shrub and grassland zone, although the most abundant homologue is n-C_(31) , relatively high n-C_(23) concentrations have also been observed in some samples. The statistical results show a good correlation between n-alkane proxies and climatic factors. The average chain length(ACL) values are positively correlated with precipitation and temperature across the transect. The carbon preference index(CPI) values show a negative correlation with temperature and precipitation along a Lhasa–Bharatpur transect. Although there is a positive relationship between ACL and temperature, it is difficult to separate the two climatic variables(temperature and precipitation) because they are well coupled in the monsoon region.     

Origin and analysis of aliphatic and cyclic hydrocarbons in northeast United Kingdom coastal marine sediments

Sediment samples from multiple sites in the North Sea Coast of England were solvent extracted and analysed by a quadruple gas chromatograph equipped with a mass spectrometer detector in order to determine the concentration and distribution of aliphatic and alicyclic n-alkanes. Results indicate that most of the organic species present in the sediment samples consisted of anthropogenically derived long chain aliphatic and alicyclic n-alkanes (_nC_{10-15, 17, 19-21, 24, 26, 27, 29, 30, 33, 35, 36, 43}), n-alkanols, n-alkanals, n-alkanones, esters as well as many volatile organic compounds (VOCs). Chemical composition of samples and relative concentration were found to vary both spatially and temporally on all scales. These variations are mainly attributable to spatial and temporal variations in source but also parameters such as rainfall, turbulence and micro-organism activity also account for the observed trends.     

塔里木盆地原油的成因研究

对塔里木盆地原油和生油岩饱和烃进行ＧＣ－Ｃ－ＭＳ和ＧＣ－ＭＳ分析，利用单个正构烷烃碳同位素组成和三环萜烷分布特征进行油源对比，研究了塔里木盆地原油的油源问题；根据寒武—奥陶系富含菌藻有机质生油岩饱和烃色谱分析结果，对塔里木盆地海相原油含蜡较高的成因进行了探讨     

Origin of organic sulphur compounds and sulphur-containing high molecular weight substances in sediments and immature crude oils

The distribution patterns of Organic Sulphur Compounds (OSC), occurring in certain sediments and immature crude oils, were compared with those of the corresponding hydrocarbons. Because of the complexity of the OSC mixtures, they were desulphurized to hydrocarbons (n-alkanes, isoprenoid alkanes, steranes, triterpanes and branched alkanes). The hydrocarbons produced by desulphurization of the OSC exhibited distribution patterns different from those of the hydrocarbons originally present. Therefore reaction of elemental sulphur with these hydrocarbons at elevated temperatures must be considered as an unlikely origin for these OSC. Sulphur incorporation reactions on an intramolecular basis with suitable functionalized precursors at the early stages of diagenesis are probably the major origin for these OSc. Desulphurization of high molecular weight fractions also produced hydrocarbons, dominated by n-alkanes up to C₄₀. Therefore it is assumed that these substances contain n-alkanes, 2,5-dialkyl-thiophenes and -thiolanes linked to each other by sulphur briddges. These findings stronly suggest that sulphur-containing high molecular weight substances are formed by the same sulphur incorporation reactions as OSC, but in an intermolecular fashion.     

The chemical structure of a pronounced series of iso-alkanes in South Oman crudes

Gas chromatograms of the saturated hydrocarbon fractions of the South Oman crudes are characterised by a striking series of peaks (called X-peaks throughout this paper) eluting between the n-alkanes mainly in the C₂₀–C₂₆ range. A GS-MS study, combined with optimised GC resolution shows that each peak is a superposition of subpeaks which correspond to a complex series of monomethylalkanes. The X₂₀ peak in the chromatogram, for instance, is found to be composed of virtually co-eluting peaks corresponding to 5-, 6-, 7-, 8-, 9- and 10-methylnonadecane. The larger X₂₂, X₂₃ and X₂₄ peaks are superpositions of a similar set of monomethylalkanes and in addition a series of (presumably) dimethylalkanes of which the structures are only partly solved. The large abundance of these iso-alkanes is very specific for South Oman crudes and may be caused by their (pre-) Cambrian origin or a specific source material.     

Monocyclic alkanes in Ordovician organic matter

The major compounds in the C₁₅₊ branched/cyclic alkane fractions of two Ordovician oils (Pine Unit and Midland Farms oils) and an immature Ordovician rock (Guttenberg Oil Rock) are monocyclics. One series of these compounds was identified as n-alkylcyclohexanes and another tentatively identified as methyl-n-alkylcyclohexanes. The carbon number distribution of these compounds resembled those of the n-alkanes found in these samples with an odd carbon number predominance. It is suggested that the monocyclic alkanes, in these Ordovician samples, may be principally derived from the cyclisation of straight-chain algal fatty acids, by mechanisms that involve decarboxylation. However, there is evidence from the m/z 97 fragmentograms of these samples, to indicate that methyl-n-alkylcyclohexanes can also be derived from fatty acids by a less preferred mechanism that does not involve decarboxylation or from other precursors.In addition, a sample of kerogen from the Guttenberg Oil Rock was hydrously pyrolysed. The saturated hydrocarbon products of this experiment showed very similar distributions (including monocyclics) to those observed in the Ordovician oils. This suggests that although the oils and the Guttenberg Oil Rock come from widely differing geographical locations, their precursor (algal derived) organic matter was very similar.     

Aliphatic components of Victorian brown coal lithotypes

Victorian brown coal occurs in five major lithotypes distinguishable by colour index, petrography and bulk chemical analyses. The distributions of solvent extractable (free) and base hydrolysable (bound) n-alkanes, n-monocar?ylic acids, n-?,ω-dicar?ylic acids, n-ω-hydroxycar?ylic acids and n-alcohols were determined for samples of each of the five lithotypes (lithotype profile) and for seven samples of identical lithotype classification spanning a 100 m interval (depth profile) taken from a continuous bore core. The distributions of free molecular components in all classes are indicative of the predominant higher plant origin of this immature coal and provide strong support for the view that different lithotypes have derived from different, yet fairly specific paleobotanical communities. Despite an overall similarity in the distributions of aliphatic components from samples of identical lithotype classification, changes in the absolute concentrations and carbon preference indices (CPIs) of specific functional classes are observed in response to catagenetic influences even across the very small rank interval of the depth profile samples. Molecular distributions of bound components are similar to those of their free counterparts except that CPIs are generally lower and the relative contributions of lower molecular weight homologues (i.e. <C₂₂) are higher. Thedistributions of bound dicar?ylic acids and hydroxycar?ylic acids appear to reflect variations in the oxic/anoxic nature of the depositional paleoenvironments.     

Comparison of lipid character of sediments from the Great Lakes and the Northwestern Atlantic

Geolipid compositions of surficial sediments from Lake Michigan, Lake Huron, and from three locations in the Northwestern Atlantic were determined to compare source inputs and alteration processes in different sedimentary environments. Fatty acids, sterols, fatty alcohols, and alkanes were examined in both unbound and bound extracts of these samples. Significant amounts of long chain fatty acids, alcohols, and hydrocarbons are present in the deep ocean station, yet this location contains a proportionally larger amount of short chain geolipids than do marine stations closer to shore. Larger proportions of long chain lipids present in the Lake Michigan, Lake Huron, and Gulf of Maine samples relative to the open ocean samples reflect larger inputs of land-derived lipids to sediments closer to terrigenous sources. Marine samples contain a more complex mixture of sterols than is found in lake sediments, suggesting that sterol inputs and alteration processes in the marine environment are more complex than in lacustrine settings. Ratios of 16:1/16:0 and 18:1/18:0 fatty acids decrease with increasing distance from land, which suggests that fatty acid degradation before and during deposition becomes more extensive in the open deeper ocean stations.