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1.
The molecular composition of fossil resins from early to middle Eocene coal from northeast India, has been analyzed for the first time to infer their paleobotanical source. The soluble component of fossil resin was analyzed using gas chromatography–mass spectrometry (GC–MS). The resin extracts are composed of cadalene-based C15 sesquiterpenoids and diagenetically altered triterpenoids. The macromolecular composition was investigated using pyrolysis gas chromatography-mass spectrometry (Py-GC–MS) and Fourier transform infrared (FTIR) spectroscopy. The major pyrolysis products are C15 bicyclic sesquiterpenoids, alkylated naphthalenes, benzenes and a series of C17–C34 n-alkene-n-alkane pairs. Spectroscopic analysis revealed the dominance of aliphatic components. The presence of cadalene-based sequiterpenoids confirms the resin to be Class II or dammar resin, derived from angiosperms of Dipterocarpaceae family. These sesquiterpenoids are often detected in many SE Asian fluvio-deltaic oils. Dipterocarpaceae are characteristic of warm tropical climate suggesting the prevalence of such climate during early Eocene in northeast India.  相似文献   

2.
The terpenoid composition of resins from the Miocene lignite horizons from the Kerala-Konkan Coast, western India was analyzed by Curie-point pyrolysis-gas chromatography-mass spectrometry (Cupy-GC-MS). The major pyrolysates were cadalene-based bicyclic sesquiterpenoids including some C30-C31 bicadinenes and bicadinanes typical of dammar resin from angiosperm plants of Dipterocarpaceae family. These plants are typically supported by tropical climates which the western Indian region was known to have experienced during early Tertiary period. The present study suggests that these palaeoclimatic conditions persisted until at least the Miocene epoch. These sesquiterpenoids which are commonly detected in many SE Asian crude oils may be utilised as useful biomarkers for petroleum exploration in the western Indian region.  相似文献   

3.
Peats in a sediment core from Ruoergai bog, which has a cold and moist plateau climate with major source input from herbaceous plants, have been studied by GC–MS in order to understand the composition and diagenetic processes of lipids in this depositional environment. Long chain components (C21–C35) predominate in the n-alkanes, n-alk-1-enes, n-fatty acids, n-alkan-2-ones and n-alkanols with a maximum of C31, C27, C22 or C24, C23 or C25 and C22, respectively. A herbaceous origin for these long chain compounds is suggested, and this is supported by their stable carbon isotopic compositions. Diterpenoid hydrocarbons with abietane, pimarane and kaurane skeletons, some of which have not been reported often in modern sediments, are prominent and are derived from higher plants. Several triterpenoid ketones and alcohols with oleanane or lupane skeletons, and a series of des-A-triterpenoid hydrocarbons which have not been reported often in modern sediments are also present, and are assigned to a higher plant source. Hopanoids, including their alkanes, alkenes, ketones, alcohols and esters, are abundant and of bacterial origin. Steroid ketones and alkanols are dominated by C29 homologues. C28 and C29 steroids are derived mainly from higher plants, whereas the C27 component is assigned to a microbial source. The presence of short-chain n-alkanes with no odd-even carbon predominance, bacterially derived fatty acids (C14, C15, iso- and unsaturated acids), n-alkan-2-ones, des-A-triterpenoid hydrocarbons, hopanoids and some steroid ketones indicate that intense microbial reworking of the organic matter has taken place in this depositional environment. The chemical and biochemical conversions of some cyclic alkenes to alkanes, such as tricyclic diterpenoids, tetracyclic terpenoids and steroid ketones, are also evident with depth. The dominance of C20 components in the diterpenoid hydrocarbons may reflect an oxidizing or reducing depositional condition.  相似文献   

4.
The chemical structure of the resin from an Australian soft brown coal (Yallourn) has been investigated by cross-polarization nuclear magnetic resonance spectroscopy with magic angle spinning (13C CP MAS NMR). Some additional solution 1H and 13C data were also obtained. Solid-state experiments were performed with and without a delay period before data acquisition. The resulting free induction decays were Fourier transformed with respect to acquisition time and delay period to produce two-dimensional solid-state spectra. Assignments made from the spectra clearly demonstrate that the gross chemical structure of the Yallourn resin is best described as a polymerized diterpenoid with one axial carboxylic group and two double bonds. One double bond is trisubstituted, the other is monosubstituted. After consideration of various mechanisms for polymerization of diterpenoid units during biogenesis and coalification, it was concluded that polymerization occurs at the C15 carbon atoms in the diterpenoids without cyclization of the methylene units at C8.  相似文献   

5.
A new fossil fruit wing of Shorea Roxb. belonging to the family Dipterocarpaceae is described from the Early Miocene sediments of Kachchh, Gujarat. It resembles best the extant species Shorea macroptera Dyer, which is a prominent member of the tropical evergreen forests of the Malayan Peninsula. The present finding, along with the other megafossil records described from the same area, indicates a typical tropical vegetation with a warm and humid climate at the time of deposition in contrast to the present day xeric vegetation in the area. As the family Dipterocarpaceae no longer exists in western India, it is essential to discuss the time of its extinction and possible causes, which may include drastic changes in the climate of the region. The present finding also supports the theory of a Malaysian origin for the family in contrast to the hypothesis of a Gondwanan origin.  相似文献   

6.
The comparison of the fatty acids between aerobic anoxygenic phototrophic bacteria (AAPB) and their phylogenetic relatives has been a fascinating but yet enigmatic topic, enhancing our understanding of physiological variations between these evolutionarily related microorganisms. Two strains of marine bacteria, both phylogenetically falling into Erythrobacter sp., were isolated from the South China Sea, and demonstrated, respectively, to be an aerobic anoxygenic phototrophic bacteria (AAPB) (JL475) which is capable of anoxygenic photosynthesis via BChl a, and an obligate heterotroph (JL316) with a lack of BChl a, on the basis of phylogenetic analysis and pure culture cultivation. Phospholipid fatty acids (PLFA) and glycolipid fatty acids (GLFA) of the two strains were extracted and analyzed by gas chromatographymass spectrometry. The PLFA in JL475 AAPB are characterized by C18:1 C18:2ω7,13 and C18:1, with the C18:2ω7,13 being a specific compound for AAPB and in particular for Erythrobacter longus and some of its phylogenetically closely related relatives. The JL316 strain is characterized in PLFA by the presence of C18:1, C16:1 and C16:0, and in particular C17:1. GLFA do not show any discrimination between the two strains. Four α,ω-dicarboxylic acids, including 1,8-octanedioic acid, 1,9-nonanedioic acid, 1,10-decanedioic acid and 1,11-undecanedioic acid, are present only in JL316 GLFA, presumably derived from metabolic products. C14-C16 2-hydroxy fatty acids were found in the two strains, probably assuming a similar function of their LPS in outer membranes.  相似文献   

7.
With a production of 208.2 m3/d, heavy oil was produced by drill stem test (DST) from three shallow reservoirs in Sand Group Nos. Ⅰ and Ⅲ of the Neogene Guantao Formation (NgⅠ and NgⅢ) and the Eogene Dongying Formation (Ed) in an exploratory well Ban-14-1 within the Qianmiqiao region, Bohai Bay Basin, northern China. Based on the GC and GC-MS data of the NgⅠ and NgⅢ heavy oil samples, all n-alkanes and most isoprenoid hydrocarbons are lost and the GC baseline appears as an evident "hump", implying a large quantity of unresolved complex mixture (UCM), which typically revealed a result of heavy biodegradation. However, there still is a complete series of C14-C73 n-alkanes in the high-temperature gas chromatograms (HTGC) of the heavy oil, among which, the abundance of C30- n-alkanes are drastically reduced. The C35-C55 high molecular weight (HMW) n-alkanes are at high abundance and show a normal distribution pattern with major peak at C43 and an obvious odd-carbon-number predominance with CPI37-55 and  相似文献   

8.
Isotopic and chemical composition of groundwater from wells and springs, and surface water from the basalt-dominated Axum area (northern Ethiopia) provides evidence for the origin of water and dissolved species. Shallow (depth < 40 m) and deep groundwater are distinguished by both chemical and isotopic composition. Deep groundwater is significantly enriched in dissolved inorganic carbon up to 40 mmol l−1 and in concentrations of Ca2+, Mg2+, Na+ and Si(OH)4 compared to the shallow type.The δ2H and δ18O values of all solutions clearly indicate meteoric origin. Shifts from the local meteoric water line are attributed to evaporation of surface and spring water, and to strong water–rock interaction. The δ13CDIC values of shallow groundwater between −12 and −7‰ (VPDB) display the uptake of CO2 from local soil horizons, whereas δ13CDIC of deep groundwater ranges from −5 to +1‰. Considering open system conditions with respect to gaseous CO2, δ13CDIC = +1‰ of the deep groundwater with highest PCO2 = 10−0.9 atm yields δ13CCO2(gas) ≈ −5‰, which is close to the stable carbon isotopic composition of magmatic CO2. Accordingly, stable carbon isotope ratios within the above range are referred to individual proportions of CO2 from soil and magmatic origin. The uptake of magmatic CO2 results in elevated cations and Si(OH)4 concentrations. Weathering of local basalts is documented by 87Sr/86Sr ratios of the groundwater from 0.7038 to 0.7059. Highest values indicate Sr release from the basement rocks. Besides weathering of silicates, neoformation of solids has to be considered, which results in the formation of, e.g., kaolinite and montmorillonite. In several solutions supersaturation with respect to calcite is reached by outgassing of CO2 from the solution leading to secondary calcite formation.  相似文献   

9.
At centennial to millennial timescales, little is known of C3 and C4 plant productivity’s responses to past regional climate changes and the dominant forcing factors during the Holocene, although large-scale changes in glacial-interglacial periods have been attributed to changes in aridity, temperature, and CO2 concentration. We investigated the δ13C of TOC, C/N ratios, and pollen in samples from a wetland on Jeju Island, Korea. The bulk isotopic signal ranging from ?17‰ to ?29‰ was partitioned into C3 and C4 plant signals by using a binary mixing model and calculating separate organic carbon-accumulation rates for C3 and C4 plants (OCAR3 and OCAR4) during the last 6500 years. Pollen data indicated that the temperate deciduous broadleaved trees replaced grassland dominated by Artemisia, dry-tolerant grass, and further expanded in the maar. The long-term decreasing trend of Artemisia-dominated grassland was similar to those of δ13C values and OCAR4. The multi-centennial to millennial variability superimposed on the gradual increasing trend of OCAR3 was inversely correlated with those of the sea surface temperature (SST) in the western tropical Pacific (WTP) and El Niño-Southern Oscillation (ENSO) activity, suggesting that C3 plants have stronger sensitivity to regional climate change driven by oceanic forcing. Our data suggest that vegetation changes in a coastal area in East Asia were affected by monsoonal changes coupled with SST in WTP and ENSO activity. The vegetation change on Jeju Island varied quite differently from change in the westerly pathway, suggesting only a weak influence from high-latitude-driven atmospheric circulation changes. We conclude that centennial- to millennial-scale climate changes in coastal regions of East Asia during the mid- to late-Holocene may have been mainly controlled by low-latitudinal oceanic forcing, including forcing by SST and ENSO activity.  相似文献   

10.
The geological record of the Neoproterozoic to early Palaeozoic Proto-Tethyan Ocean in Southeast Asia is not clear. To better constrain the evolution of the Proto-Tethys, we present new geochronology, geochemistry, and petrology of the late Cambrian to Ordovician Pinghe pluton monzogranite from the Baoshan block, western Yunnan, southwest China. Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) analyses of four zircon samples yield ages of 482–494 and 439–445 Ma for the pluton, interpreted as two episodes within one magmatic event accompanying the whole process of subduction–collision–orogeny between buoyant blocks and oceanic crust of the Proto-Tethys. The monzogranite belongs to the strong peraluminous, high-K, calc-alkaline series and shows characteristics of both I-type and S-type granitic rocks. It is characterized by extremely high Rb/Sr and Rb/Ba but low TiO2, MgO, FeOt, and CaO/Na2O ratios. The monzogranite is also moderately enriched in light rare earth elements (LREEs), depleted in heavy rare earth elements (HREEs), lacks HREE fractionation, and has strongly negative Eu (Eu/Eu* = 0.06–0.49), Ba, Nb, Ta, Sr, and Ti anomalies. Whole-rock εNd(t) and εHf(t) values range from ?8.7 to ?11.6 and ?5.55 to ?9.58, respectively. Nd and Hf two-stage model ages range from 1.66 to 2.06 Ga and 2.14 to 3.00 Ga, respectively, with variable radiogenic 206Pb/204Pb(t) (16.547–18.705), 207Pb/204Pb(t) (15.645–15.765), and 208Pb/204Pb(t) (38.273–38.830). These signatures suggest that the monzogranite magma was derived from partial melting of heterogeneous metapelite, which was generated from Neoarchean to Palaeoproterozoic materials mixed with basaltic magma. The monzogranite magma underwent crystallization differentiation of plagioclase, K-feldspar, and ilmenite. Magmatism to form the Pinghe pluton occurred in a post-collisional setting. Based on the comparison of coeval granites throughout adjacent regions (e.g. Himalayan orogen, Lhasa Terrane, and parts of Gondwana supercontinent), we propose that the Baoshan block was derived from the northern Australian Proto-Tethyan Andean-type active continental margin of Gondwana and experienced subduction of the Proto-Tethyan oceanic crust and accretion of an outboard micro-continent. The Pinghe pluton could have formed when a subducting oceanic slab broke off during collision.  相似文献   

11.
The physical and chemical properties of 8 samples of amber from different localities in Poland (Baltic Coast, Bełchatów Tertiary brown coal, and Jaroszów clay mine) were investigated by N2 sorption at 77 K, positron annihilation spectroscopy for chemical analysis (PASCA) and by organic geochemical methods (FT-IR,1H and13C NMR, GC, and GC-MS). The porosity of the ambers as determined by PASCA consists of narrow micropores with diameters ranging from 0.8 to 0.9 nm and a volume 0.025 cm3 g−1. In the external eroded part of the amber samples (rind) the concentration of pores where positronium atoms can form is lower and consists of approximately12 the concentration as in their interior. Values of pore parameters determined from sorption of N2 are comparable with those found by the PASCA method. The average diameter of pores ranges from 2 to 12 nm, while their volume varies from 0.018 to 0.048 cm3 g−1.. The chemical character of the ambers is similar based on FT-IR spectroscopy. However, noticeable differences in concentrations of ester and hydroxyl groups are observed in both exterior and interior regions, where the abundances of the ester groups are lower in the exterior rind. The proportion of organic material extractable with chloroform-methanol (1:1, v/v) ranges from 15 to 50% and correlates inversely to the average reflectances (Rr) of polished amber surfaces which range from 1.7 to 0.1 %. These variations are attributed to differing concentrations of oxygenated groups in the respective amber samples. The FT-IR spectra of the non-polar fractions (NP) from the extracts resemble the spectra of the source ambers. However, the intensities of the absorbance for the hdroxyl group are much lower, while absorbances for exomethylene groups are not present. The1H and13C NMR data of NP fractions showed a complex diversity of components in mixtures with different relative concentrations but predominantly aliphatic in character for the respective samples.GC and GC-MS analyses of these fractions revealed that they are comprised of a mixture of compounds typical for Baltic amber but with variable relative concentrations. Two groups of compounds are found to be common to all NP fractions. The first is a minor concentration of homologousn-alkanes with a characteristic Gaussian distribution in the range from C22 to C32 and maximizing at C26–C27. In addition C22 is characteristically slightly higher in concentration compared to C23. The second group of compounds is comprised of succinates with methyl, fenchyl, bomyl and isobornyl alcohols. The composition of these diesters revealed the same equilibrium ratio between compounds with fenchyl, bornyl and isobornyl alcohols in all NP fractions. We suggest an early enzymatically controlled (bacterial) process in the formation of succinates during resin diagenesis from the biotic precursors, yielding the same characteristic ratio of the respective succinates in these ambers. These results show that all the ambers analyzed here fall into a common class of fossil resin, succinite (class Ia) independent of the sample location in Poland.  相似文献   

12.
The origin of felsic magmas (>63% SiO2) in intra-oceanic arc settings is still a matter of debate. Two very different processes are currently invoked to explain their origin. These include fractional crystallization of basaltic magma and partial melting of lower crustal amphibolite. Because both fractionation and melting can lead to similar major element, trace element and isotopic characteristics in felsic magmas, such lines of evidence have been generally unsuccessful in discriminating between the two processes. A commonly under-appreciated aspect of rare earth element (REE) solid–liquid partitioning behavior is that D REE for most common igneous minerals (especially hornblende) increase significantly with increasing liquid SiO2 contents. For some minerals (e.g., hornblende and augite), REE partitioning can change from incomptatible (D < 1) at low liquid SiO2 to compatible (D > 1) at high liquid SiO2. When this behavior is incorporated into carefully constrained mass-balance models for mafic (basaltic) amphibolite melting, intermediate (andesitic) amphibolite melting, lower or mid to upper crustal hornblende-present basalt fractionation, and mid to upper crustal hornblende-absent basalt fractionation the following general predictions emerge for felsic magmas (e.g., ∼63 to 76% SiO2). Partial melting of either mafic or intermediate amphibolite should, regardless of the type of melting (equilibrium, fractional, accumulated fractional) yield REE abundances that remain essentially constant and then decrease, or steadily decrease with increasing liquid SiO2 content. At high liquid SiO2 contents LREE abundances should be slightly enriched to slightly depleted (i.e., C l/C o ∼ 2 to 0.2) while HREE abundances should be slightly depleted (C l/C o ∼ 1 to 0.2). Lower crustal hornblende-bearing basalt fractionation should yield roughly constant REE abundances with increasing liquid SiO2 and exhibit only slight enrichment (C l/C o ∼ 1.2). Mid to upper crustal hornblende-bearing basalt fractionation should yield steadily increasing LREE abundances but constant and then decreasing HREE abundances. At high liquid SiO2 contents LREE abundances may range from non-enriched to highly enriched (C l/C o ∼ 1 to 5) while HREE abundances are generally non-enriched to only slightly enriched (C l/C o ∼ 1 to 2). Hornblende-absent basalt fractionation should yield steadily increasing REE abundances with increasing liquid SiO2 contents. At high SiO2 contents both LREE and HREE are highly enriched (C l/C o ∼ 3 to 4). It is proposed that these model predictions constitute a viable test for determining a fractionation or amphibolite melting origin for felsic magmas in intra-oceanic arc environments where continental crust is absent. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.
James G. BrophyEmail:
  相似文献   

13.
Significantly high abundant methyl-MethylTrimethylTridecylChromans (MTTCs) have been detected in aromatic hydrocarbon fractions in crude oils from the Jizhong Depression and Jianghan Basin. The distribution of these compounds is dominated by methyl-MTTC and dimethyl-MTTC series, which indicate diagenetic products of a hypersaline depositional environment in the early stage and show a low degree of methylation. The occurrence of significantly high abundant methyl-MTTC depends mainly on good preservation conditions with a strongly reductive, hypersaline and water-columned depositional environment and subsequent non-intensive diagenetic transformations. The stable carbon isotopic compositions of the methyl-MTTCs and dimethyl-MTTCs in two samples are far different from the stable carbon isotopic composition of C30 hopane of apparent bacteria biogenesis (up to 4.11‰ and 5.75‰, respectively). This obviously demonstrates that the methyl-MTTC and dimethyl-MTTCs cannot be of bacteria origin, which is different from the previous point of view about non-photosynthetic bacteria products or possible bacteria-reworked products. On the contrary, the stable carbon isotopic compositions of methyl-MTTC and dimethyl-MTTCs in the two samples were similar to that of the same carbon-numbered n-alkanes (nC27-nC28-nC29), which indicates that they share the same source origin. Especially in the crude oil from the Zhao61 well, stable carbon isotopic compositions are also similar to that of the same carbon-numbered steranes with ααα-20R isomer (mostly less than 0.4‰). In consideration of the results of previous studies on saline lake ecological sedimentation, the authors hold that the methyl-MTTC and dimethyl-MTTCs in the saline lake sediments should be of algal biogenesis origin.  相似文献   

14.
We review the current knowledge about Southeast Asian volcanoes and their eruption histories, and focus on identifying tephrochronologic markers representing major explosive eruptions in order to further future palaeoclimate and volcanological studies. Forty-one volcanic edifices in Southeast Asia have been classified as large calderas by Whelley et al. (2015) and thus have, or are likely to have, produced large explosive eruptions with a Volcanic Explosivity Index (VEI) of 6–8. Unfortunately, only 20 such eruptions have known ages, spanning from 1.2 Ma to 1991 ad , and fewer have geochemical data that can be used for tephrostratigraphic correlations. Volcanic products from different geodynamic regions and different sources can generally be distinguished on major element plots (e.g. K2O versus CaO) of matrix glass composition. However, the distinction of multiple eruptions from the same source often requires additional data such as trace element compositions of matrix glass and/or mineral compositions. Biotite, but also magnetite compositions (MgO and TiO2 content in particular) appear to be very discriminating. Up to nine tuffs in addition to the three to four Toba tuffs can be utilised as widespread tephrochronologic markers and span a range from 1.2 to 1.6 Ma to recent. As only a few Holocene major eruptions have been well characterised and dated, many large calderas are still unstudied, and many distal tephra layers are still lacking a source, more tephrochronologic markers can certainly be defined in the future.  相似文献   

15.
Hydrocarbon mixtures too complex to resolve by traditional capillary gas chromatography display gas chromatograms with dramatically rising baselines or “humps” of coeluting compounds that are termed unresolved complex mixtures (UCMs). Because the constituents of UCMs are not ordinarily identified, a large amount of geochemical information is never explored. Gas chromatograms of saturated/unsaturated hydrocarbons extracted from Late Archean argillites and greywackes of the southern Abitibi Province of Ontario, Canada contain UCMs with different appearances or “topologies” relating to the intensity and retention time of the compounds comprising the UCMs. These topologies appear to have some level of stratigraphic organization, such that samples collected at any stratigraphic formation collectively are dominated by UCMs that either elute early- (within a window of C15–C20 n-alkanes), early- to mid- (C15–C30 n-alkanes), or have a broad UCM that extends through the entire retention time of the sample (from C15–C42 n-alkanes). Comprehensive two-dimensional gas chromatography time-of-flight mass spectrometry (GC×GC–MS) was used to resolve the constituents forming these various UCMs. Early- to mid-eluting UCMs are dominated by configurational isomers of alkyl-substituted and non-substituted polycyclic compounds that contain up to six rings. Late eluting UCMs are composed of C36–C40 mono-, bi-, and tricyclic archaeal isoprenoid diastereomers. Broad UCMs spanning the retention time of compound elution contain nearly the same compounds observed in the early-, mid-, and late-retention time UCMs. Although the origin of the polycyclic compounds is unclear, the variations in the UCM topology appear to depend on the concentration of initial compound classes that have the potential to become isomerized. Isomerization of these constituents may have resulted from hydrothermal alteration of organic matter.  相似文献   

16.
The geochemical composition of lake bed sediments of a tropical reservoir in Brazil have been investigated. The C, N, P composition showed almost no variation between the different sampling points. All samples contained inorganic phosphorus (IP) ranging from 52 to 70%. The Redfield ratios show that the lake is without significant anthropogenic inputs. Most of the organic matter is composed by higher plants decomposition revealed in the total organic carbon (TOC):nitrogen (N) ratio ranging from 15.4 to 57.2. Also, TOC:organic phosphorus (OP) ranged from 265.3 to 933.6, suggesting that most of the organic matter has terrestrial origin from wood plants. The ratios suggest that most organic matter is influenced by the terrestrial characteristics of the watershed. Furthermore, the relative abundance of n-alkane homologues in the sediments was investigated. All samples have been analyzed for the n-alkanes C8 to C40. The sediments were dominated by n-alkanes C25–C38. It is concluded that n-alkane in sediments mainly come from terrestrial plants, however there is a contribution of submerged aquatic plants, especially in those sites in deeper areas of the lake. On the basis of Paq index the n-alkanes in sediments comes from terrestrial plants, however there is a contribution from emerged/floating plants.The investigated lake seems to be considered as meso to eutrophic. Because of the relatively high primary productivity in the lakes, there is a substantial organic-matter flux to the sediments, which rapidly becomes anoxic. According to the pristine/phytane ratio the sediments represent an anoxic environment with values found between 0.38 and 1.72.  相似文献   

17.
A geochemical study of surface sediments from Pranhita-Godavari Basin, Andhra Pradesh, India was carried out using light hydrocarbon compounds to assess the hydrocarbon potential of the basin. Suite of 80 soil samples were collected from the depth of 2.5 m and analyzed for adsorbed light gaseous hydrocarbons namely methane (CH4), ethane (C2H6) and propane (C3H8) in Gas chromatograph. Compound specific Carbon isotope ratios for CH4 and C2H6 were also determined using GC-C IRMS (Gas Chromatograph Combustion Isotope Mass Spectrometer). The presence of moderate to low concentrations of methane (CCH4 C_{CH_4 } : 1 to 138 ppb), ethane (H4{H_4 }: 1 to 35 ppb) and propane (CC3 H8 C_{C_3 H_8 } : 1 to 20 ppb) was measured in the soil samples. Carbon isotopic composition of d13 CCH4 \delta ^{13} C_{CH_4 } ranges between −27.9 to −47.1 ‰ and d13 CC2 H6 \delta ^{13} C_{C_2 H_6 } ranged between −36.9 to −37.2 ‰ (V-PDB) indicating that these gases are of thermogenic origin. Study of soil samples suggests the area has good potential for hydrocarbon.  相似文献   

18.
《International Geology Review》2012,54(15):1823-1841
ABSTRACT

The Song Ma zone in Northwestern Vietnam is considered as a suture of the South China and Indochina blocks, and plays an important role in understanding the tectonic evolution in Southeast Asia and surrounding areas. Granitic rocks of the Muong Lat complex are distributed in the Song Ma suture, consisting mainly of monzogranite and granodiorite. The rocks are sub-alkaline in affinity with high K contents and characteristics of S-type granite. They have high SiO2, total Na2O + K2O, and Zr contents and high aluminium saturation index values (0.97 to 1.29 with an average of 1.14). All these geochemical signatures, together with high (87Sr/86Sr)i ratios (0.71391 to 0.74568), and low whole rock εNd(t) and zircon εHf(t) values (?13.1 to ?9.4) suggested an origin from partial melting of crustal source rocks. Primitive mantle normalized trace element contents exhibit positive anomalies of Rb, Th, U and Pb, but negative anomalies of Nb, Ta, and Ti, indicating a collision-related environment. The depleted Nd and Hf zircon model ages from investigated samples, in combination with inherited zircon ages, suggest the existence of Precambrian basement in the study region. S-type granites of the late Permian-early Triassic (the Muong Lat, Phia Bioc and Hai Van complexes) in Vietnam were formed by the subduction-collision of the South China and Indochina blocks.  相似文献   

19.
The compositions of sterol, alcohol and ketone fractions from an oxic intertidal surface sediment from Corner Inlet. Victoria, Australia, have been examined by capillary gas chromatographymass spectrometry and related to the lipids of diatoms cultured from the sediment and to lipids of the sea-grass Zostera muelleri. Of the more than thirty sterols in the sediment most appear to derive from diatoms, including the major sterol 24-methylcholesta-5.22E-dien-3β-ol. Small amounts of 24-ethylcholesterol probably derive from Zostera, with a minor diatom contribution. 5α-stanols, both fully saturated and with a side-chain double bond, represented ca. 14% of the total sterols: a significant proportion of these are probably derived from marine invertebrates. These organisms also contribute C26 sterols. most of the cholesterol and possibly small amounts of Δ-sterols. The data suggest that in situ biohydrogenation of stenols was not a major process in sterol transformation in the surface oxic sediment. Alcohols ranged from C12 to C30 and showed an unusual abundance of unsaturated components with Δ9-16:1 being the major constituent. The long-chain alcohols probably originate largely from Zostera but the shorter-chain. C12-C20. alcohols are at least partly derived from wax esters of unknown origin. Diatoms do not contribute significant amounts of alcohols. Ketones were not major constituents of the sediment and consisted mainly of 6.10.14-trimethylpentadecan-2-one and a series of n-alkan-2-ones ranging from C16 to C33. The latter showed a similar distribution to that of the n-alkanes but the correspondence was not sufficient to substantiate a product-precursor relationship. Very long-chain C3- C39 unsaturated methyl and ethyl ketones, which may originate from the marine unicellular alga Emiliania huxleyi. were present in low concentration.  相似文献   

20.
During the Quaternary glacial episodes, when sea level was considerably lower, Asia and North America were linked by large extensions of circumarctic land (Beringia), which remained unglaciated. This land mass served not only as a biogeographical bridge for plants, animals, and humans, but also supported a biome very different from present tundra or boreal coniferous forests, which was dominated by steppes and a rich mammalian megafauna. Carbon stable isotope ratios of Beringian late Pleistocene mummified remains of bison, equids, mammoth, caribou, musk-ox, moose, woolly rhino, and other undetermined species, found preserved in permafrost, indicate that these megaherbivores fed exclusively on C3 plants, and that C4 grasses were not differentially ingested by bison, as previously suggested. Paleoclimatic constraints probably prevented the formation of a warm-season (C4) guild during the later part of the growing season in the steppes of Beringia during the last glaciation.  相似文献   

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