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1.
The Ordos Basin, the second largest sedimentary basin in China, contains the broad distribution of natural gas types. So far, several giant gas fields have been discovered in the Upper and Lower Paleozoic in this basin, each having over 1000×108m3 of proven gas reserves, and several gas pools have also been discovered in the Mesozoic. This paper collected the data of natural gases and elucidated the geochemical characteristics of gases from different reservoirs, and then discussed their origin. For hydrocarbons preserved in the Upper Paleozoic, the elevated δ 13C values of methane, ethane and propane indicate that the gases would be mainly coal-formed gases; the singular reversal in the stable carbon isotopes of gaseous alkanes suggests the mixed gases from humic sources with different maturity. In the Lower Paleozoic, the δ 13C1 values are mostly similar with those in the Upper Paleozoic, but the δ 13C2 and δ 13C3 values are slightly lighter, suggesting that the gases would be mixing of coal-type gases as a main member and oil-type gases. There are multiple reversals in carbon isotopes for gaseous alkanes, especially abnormal reversal for methane and ethane (i.e. δ 13C1>δ 13C2), inferring that gases would be mixed between high-mature coal-formed gases and oil-type gases. In the Mesozoic, the δ 13C values for gaseous alkanes are enriched in 12C, indicating that the gases are mainly derived from sapropelic sources; the carbon isotopic reversal for propane and butane in the Mesozoic is caused by microbial oxidation and mixing of gases from sapropelic sources with different maturity. In contrast to the Upper Paleozoic gases, the Mesozoic gases are characterized by heavier carbon isotopes of iso-butane than normal butane, which may be caused by gases generated from different kerogen types. Finally, according to δ 13C1-R 0 relationship and extremely low total organic carbon contents, the Low Paleozoic gases would not be generated from the Ordovician source as a main gas source, bycontrast, the Upper Paleozoic source as a main gas source is contributed to the Lower Paleozoic gases.  相似文献   

2.
Oils, condensates and natural gases in the Kekeya Field, southeast depression of the Tarim Basin were studied for their geochemical characteristics. According to the distribution analysis of the C2/C3 values with C1/C2 values, C2/C3 values with C1/C3 values, as well as C2/C3 values with dryness index, there are two different types of natural gases in the studied field, which are spatially regularly distributed. One is the oil cracking gas, located on shallow reservoirs over X 5 2 reservoir, namely Upper oil legs; the other is kerogen cracking gas, located on X 7 2 reservoirs, X8 reservoirs and E2 k reservoirs, namely Lower oil legs. In addition, the distribution patterns of molar concentration of oils and condensates with different carbon numbers of the n-alkanes in the Kekeya Field indicate that the crude oils have experienced several kinds of secondary alterations, which were closely related to the charging of gaseous hydrocarbons after petroleum accumulation. These results indicate that, based on the research of δ 13C values of individual hydrocarbons, heptane values and isoheptane values of light hydrocarbons and aromatic maturity parameters for oils, condensates and natural gases, oils and gases were charged at different geological time in the Kekeya Field.  相似文献   

3.
According to gas compositional and carbon isotopic measurement of 114 gas samples from the Kuqa depression, accumulation of the natural gases in the depression is dominated by hydrocarbon gases, with high gas dryness (C1/C1–4) at the middle and northern parts of the depression and low one towards east and west sides and southern part. The carbon isotopes of methane and its homologues are relatively enriched in 13C, and the distributive range of δ 13C1, δ 13C2 and δ 13C3 is ?32‰–?36‰, ?22‰–?24‰ and ?20‰–?22‰, respectively. In general, the carbon isotopes of gaseous alkanes become less negative with the increase of carbon numbers. The δ 13 \(C_{CO_2 } \) value is less than ?10‰ in the Kuqa depression, indicating its organogenic origin. The distributive range of 3He/4He ratio is within n × 10?8 and a decrease in 3He/4He ratio from north to south in the depression is observed. Based on the geochemical parameters of natural gas above, natural gas in the Kuqa depression is of characteristics of coal-type gas origin. The possible reasons for the partial reversal of stable carbon isotopes of gaseous alkanes involve the mixing of gases from one common source rock with different thermal maturity or from two separated source rock intervals of similar kerogen type, multistages accumulation of natural gas under high-temperature and over-pressure conditions, and sufficiency and diffusion of natural gas.  相似文献   

4.
The Xushen gas field, located in the north of Songliao Basin, is a potential giant gas area for China in the future. Its proved reserves have exceeded 1000×108 m3 by the end of 2005. But, the origin of natural gases from the deep strata is still in debating. Epimetamorphic rocks as a potential gas source are widely spreading in the northern basement of Songliao Basin. According to pyrolysis experiments for these rocks in the semi-confined system, gas production and geochemistry of alkane gases are discussed in this paper. The Carboniferous-Permian epimetamorphic rocks were heated from 300°C to 550°C, with temperature interval of 50°C. The gas production was quantified and measured for chemical and carbon isotopic compositions. Results show that δ 13C1 is less than ?20‰, carbon isotope trend of alkane gas is δ 13C1<δ 13C2<δ 13C3 or δ 13C1<δ 13C2>δ 13C3, these features suggest that the gas would be coal-type gas at high-over maturity, not be inorganic gas with reversal trend of gaseous alkanes (δ 13C1>δ 13C2>δ 13C3). These characteristics of carbon isotopes are similar with the natural gas from the basin basement, but disagree with gas from the Xingcheng reservoir. Thus, the mixing gases from the pyrolysis gas with coal-typed gases at high-over maturity or oil-typed gases do not cause the reversal trend of carbon isotopes. The gas generation intensity for epimetamorphic rocks is 3.0×108–23.8×108 m3/km2, corresponding to R o from 2.0% to 3.5% for organic matter.  相似文献   

5.
Natural gases discovered up to now in Lishui Sag, the East China Sea Basin, differ greatly in gaseous compositions, of which hydrocarbon gases amount to 2%–94% while non-hydrocarbon gases are dominated by CO2. Their hydrocarbon gases, without exception, contain less than 90% of methane and over 10% of C2 + heavier hydrocarbons, indicating a wet gas. Carbon isotopic analyses on these hydrocarbon gases showed that δ 13C1, δ 13C2 and δ 13C3 are basically lighter than ?44‰, ?29‰ and ?26‰, respectively. The difference in carbon isotopic values between methane and ethane is great, suggesting a biogenic oil-type gas produced by the mixed organic matter at peak generation. δ 13 \(C_{CO_2 } \) values of nonhydrocarbon gases are all heavier than ?10‰, indicating a typical abiogenic gas. The simulation experiment on hydrocarbon generation of organic matter in a closed gold-tube system showed that the proportion of methane in natural gases produced by terrigenous organic matter in the Lingfeng Formation marine deposit is obviously higher than that in natural gases derived from the aquatic and terrigenous mixed organic matter in the Yueguifeng Formation lacustrine deposit, consequently the proportion of heavier hydrocarbons of the former is remarkably lower than that of the latter. Moreover, δ 13C1 values of natural gases produced by terrigenous organic matter in the Lingfeng Formation marine deposit are about 5‰ heavier than those of natural gases derived from the aquatic and terrigenous mixed organic matter in the Yueguifeng Formation lacustrine deposit while δ 13C2 and δ 13C3 values of the former are over 9‰ heavier than those of the latter. Currently the LS36-1 oil-gas pool is the only commercial oil-gas reservoir in Lishui Sag, where carbon isotopic compositions of various hydrocarbon components differ greatly from those of natural gases produced by the Lingfeng Formation organic matter but are very similar to those of natural gases derived from the Yueguifeng Formation organic matter, therefore, natural gases in the LS36-1 oil-gas pool are mainly derived from the Yueguifeng Formation lacustrine source rock rather than the Lingfeng Formation marine or Mingyuefeng Formation coal-measures source rocks.  相似文献   

6.
The light hydrocarbon composition of 209 natural gas samples and individual light hydrocarbon carbon isotopes of 53 natural gas samples from typical humic-sourced gas and sapropelic-sourced gas in the four basins of China have been determined and analyzed. Some identification parameters for humic-sourced gas and sapropelic-sourced gas are proposed or corrected. The differences of compound-specific δ 13C value of individual light hydrocarbon between humic-sourced gas and sapropelic-sourced gas have been founded. The humic-sourced gas has the distribution of δ 13Cbenzene> ?24‰, δ 13Ctoluene >?23‰, δ 13Ccyclohexane > ?24‰ and δ 13Cmethyl cyclohexane> ?24‰, while the sapropelic-sourced gas has the distribution of δ 13Cbenzene <?24‰, δ 13Ctoluene< ?24‰, δ 13Ccyclohexane< ?24‰ and δ 13Cmethyl cyclohexane< ?24‰. Among the components of C7 light hydrocarbon compound, such as normal heptane (nC7), methyl cyclohexane (MCH) and dimethyl cyclopentane (ΣDMCP), etc, relative contents of nC7 and MCH are influenced mainly by the source organic matter type of natural gas. Therefore, it is suggested that the gas with relative content of nC7 of more than 30% and relative content of MCH of less than 70% is sapropelic-sourced gas, while gas with relative content of nC7 of less than 35% and relative content of MCH of more than 50% is humic-sourced gas. Among components of C5–7 aliphatics, the gas with relative content of C5–7 normal alkane of more than 30% is sapropelic-sourced gas, while the gas with relative content of C5–7 normal alkane of less than 30% is humic-sourced gas. These paremeters have been suggested to identify humic-sourced gas and sapropelic-sourced gas.  相似文献   

7.
Lower Cretaceous C-isotope records show intermittent negative/positive spikes, and consistent patterns of coeval chemostratigraphic curves thus document shifts that signal simultaneous responses of temporal changes in the global carbon reservoir. The standard pattern registered by the δ 13Corg and δ 13Ccarb in Lower Aptian sediments includes distinct isotope segments C1 to C8 (Menegatti et al., 1998). In the El Pui section, Organyà Basin, Spain, C-isotope segment C2 is the longest interval preceding segments C3–C6 associated with oceanic anoxic event 1a (OAE 1a), and reveals a distinct negative shift of ~1.8‰ to ~2.23‰ defining the C-isotope pattern within that interval. Total inorganic carbon (TIC), total organic carbon (TOC), δ 13Corg, microfacies, n-alkanes show no difference before, during, or after the negative inflection. The biomarkers indicate that organic matter (OM) mainly originates from algal/microbial sources because short-chain length homologues (≤nC19) dominate. nC20 through nC25 indicate some contribution from aquatic vegetation, but little from higher plants (>nC25), as also suggested by the terrestrial/aquatic ratio of n-alkanes or (TAR) = [(nC27+nC29+nC31)/(nC15+nC17+nC19)] (averages 0.085). We suggest that conjoint pulses of contemporaneous LIPs (Ontong Java) and massive explosive volcanism in northeast Asia, the Songliao Basin (SB-V), best conform to plausible causes of the negative intra-C2 carbon isotopic excursion (CIE) at that time. Because of its apparent common occurrence the intra-C2 inflection could be a useful marker harbinger to the more pronounced CIE C3, the hallmark of OAE1a.  相似文献   

8.
In the processes of discrimination between oil-cracked gases and kerogen-cracked gases, Behar and Pinzgofer et al.’s results were adopted in the former researches, in which the ratio of C2/C3 is basically a constant while the ratio of C1/C2 gradually increases in the course of primary cracking of kerogen. Otherwise in the course of secondary cracking of oil, the ratio of C2/C3 increases rapidly while C1/C2 keeps relatively stable. Our study on analogue experiment shows that, whether it is oil or kerogen, in its process of gas generating by cracking, the ratios of C2/C3, C1/C2 or C1/C3 will all be increased with the growth of thermal conditions. In comparison, the ratio of C2/C3, which is affected by genetic type to some comparatively less extent, mainly responds to the maturity of gases, while the value of C2/C3 is about 2, and that of C2/iC4 is about 10, and the corresponding value of R o is about 1.5%–1.6%. The influence of gas source on C2/C3 is less than that of gas maturity, otherwise C1/C2 (or C1/C3) is obviously affected by cracking matrices. The ratios of C1/C2, C1/C3 of oil-cracked gases are less than that of kerogen-cracked gases, under the condition that the ratios of C2/C3 are similar in value, so are the value of dryness indexes. There exists wide diffidence between this view and the former discrimination method in theory. The analysis of the spot sample indicates that we can apply the above basic view to dealing efficiently with the problem of the discrimination between oil-cracked gas and kerogen-cracked gas.  相似文献   

9.
Abundant natural gas inclusions were found in calcite veins filled in fractures of Central Fault Belt across the centre of Ordos Basin. Time of the calcite veins and characteristics of natural gas fluid inclusion were investigated by means of dating of thermolum luminescence (TL) and analyzing stable isotope of fluid inclusion. Results show that natural gas inclusion formed at 130–140°C with salinity of 5.5 wt%–6.0 wt% NaCl. It indicates that natural gas inclusion is a kind of thermal hydrocarbon fluid formed within the basin. Method of opening inclusion by heating was used to analyze composition of fluid inclusion online, of which the maximal hydrocarbon gas content of fluid inclusion contained in veins is 2.4219 m3/t rock and the maximal C1/ΣC i ratio is 91%. Laser Raman spectroscopy (LRS) was used to analyze chemistry of individual fluid inclusion in which the maximal hydrocarbon gas content is 91.6% compared with little inorganic composition. Isotope analysis results of calcite veins show that they were deposited in fresh water, in which the δ 13CPDB of calcite veins is from ?5.75‰ to 15.23‰ and δ 18OSMOW of calcite veins is from 21.33‰ to 21.67‰. Isotope results show that δ 13C1 PDB of natural gas fluid inclusion is from ?21.36‰ to ?29.06‰ and δDSMOW of that is from ?70.89‰ to ?111.03‰. It indicates that the gas of fluid inclusion formed from coal source rocks and it is the same as that of natural gas of Mizhi gas reservoir. Results of TL dating show that time of calcite vein is (32.4±3.42)×104 a, which is thought to be formation time of gas inclusion. It indicated that natural gas inclusion contained in calcite veins recorded natural gas leakage from Mizhi gas reservoir through the Central Fault Belt due to Himalayan tectonic movement.  相似文献   

10.
The compound-specific stable carbon isotope compositions(δ~(13)C) of leaf wax n-alkanes from two short sediment cores recovered off the Pearl River estuary(PRE) were analyzed to check for their capability of indicating decadal scale catchment environmental change. Sedimentary long-chain n-alkanes exhibited an odd-over-even predominance, with a maximum at n-C_(29) or n-C_(31), indicating their leaf wax origin was from vascular plants. The δ~(13)C values of C_(29) and C_(31) n-alkane in all the sediment samples were in the range of -28.8‰ to -31.2‰, consistent with the C_3 plant-dominated vegetation in the Pearl River catchments. The time series of δ~(13)C records from the two cores were comparable and displayed a decreasing trend from the early 20 th century to the end of the 1970s, followed by a reversal in that change leading to continued increase for ca. 15 years. After being corrected for the effect of atmospheric CO_2 rise and δ~(13)C_(atm) decline, the δ~(13)C_(29) records largely retained their raw changing pattern; the post-1980 increase being more conspicuous. The slightly decreasing trend in corrected δ~(13)C records before around 1980 may have been caused by an increase in precipitation, whereas the subsequent increase of δ~(13)C is likely associated with the observed dry climate and/or intensive anthropogenic deforestation. Our results thus demonstrate that leaf wax n-alkanes buried in the sediments off the PRE may well reflect change in the regional climate and/or human activity in the river catchments over the past century.  相似文献   

11.

Oils, condensates and natural gases in the Kekeya Field, southeast depression of the Tarim Basin were studied for their geochemical characteristics. According to the distribution analysis of the C2/C3 values with C1/C2 values, C2/C3 values with C1/C3 values, as well as C2/C3 values with dryness index, there are two different types of natural gases in the studied field, which are spatially regularly distributed. One is the oil cracking gas, located on shallow reservoirs over X 25 reservoir, namely Upper oil legs; the other is kerogen cracking gas, located on X 27 reservoirs, X8 reservoirs and E2 k reservoirs, namely Lower oil legs. In addition, the distribution patterns of molar concentration of oils and condensates with different carbon numbers of the n-alkanes in the Kekeya Field indicate that the crude oils have experienced several kinds of secondary alterations, which were closely related to the charging of gaseous hydrocarbons after petroleum accumulation. These results indicate that, based on the research of δ 13C values of individual hydrocarbons, heptane values and isoheptane values of light hydrocarbons and aromatic maturity parameters for oils, condensates and natural gases, oils and gases were charged at different geological time in the Kekeya Field.

  相似文献   

12.
Two rock samples with different structures and materials were deformed under a biaxial loading system, and multipoint strain measurements were performed for each sample. The distribution of strain anomalies during the deformation and the instability process were analyzed by using C v value put forward by WANG Xiao-qing and CHEN Xue-zhong, et al, a parameter to describe the heterogeneous distribution of earthquake precursors, so as to examine the method of C v value and to explore its physical meaning experimentally. The result shows that the change of C v value is correlated to the change of deformation characteristics and is an effective parameter to describe the heterogeneity of precursor distribution. C v value increases firstly and then decreases before the instability, and the instability occurs when C v value decreases to the level before increasing. This indicates that C v value may be a useful parameter for earthquake prediction.  相似文献   

13.
In the Tarim Basin, black shale series at the bottom of Cambrian is one of the important marine facies hydrocarbon source rocks. This research focuses on the analysis of the isotope of noble gas of 11 cherts. The R/R a ratio of chert in the Keping area is 0.032–0.319, and 40Ar/36Ar is 338–430. In Quruqtagh the R/R a ratio is 0.44–10.21, and 40Ar/36Ar is 360–765. The R/R a ratio of chert increases with 40Ar/36Ar from the west to the east accordingly. They have evolved from the crust source area to the mantle source area in a direct proportion. Surplus argon 40ArE in chert is in direct proportion to the R/R a ratio, indicating that it has the same origin of excess argon as in fluid and mantle source helium. Comparison of the R/R a ratios between the west and the east shows that the chert in the eastern part formed from the activity system of the bottom hydrothermal venting driven by the mantle source, where the material and energy of crust and mantle had a strong interaction in exchange; whereas in the western part, chert deposited from the floating of hydrothermal plume undersea bottom, which is far away from the centre of activities of the hydrothermal fluid of ocean bottom. In addition, from noble gas isotope composition of chert, it is suggested that the ocean anoxia incident happened at the black shale of the Cambrian bottom probably because of the large-scaled ocean volcanoes and the following hydrothermal activities.  相似文献   

14.
A semiempirical mathematical model of iron and manganese migration from bottom sediments into the water mass of water bodies has been proposed based on some basic regularities in the geochemistry of those elements. The entry of dissolved forms of iron and manganese under aeration conditions is assumed negligible. When dissolved-oxygen concentration is <0.5 mg/L, the elements start releasing from bottom sediments, their release rate reaching its maximum under anoxic conditions. The fluxes of dissolved iron and manganese (Me) from bottom sediments into the water mass (J Me) are governed by the gradients of their concentrations in diffusion water sublayer adjacent to sediment surface and having an average thickness of h = 0.025 cm: \({J_{Me}} = - {D_{Me}}\frac{{{C_{Me\left( {ss} \right)}} - {C_{Me\left( w \right)}}}}{h}\) (D Me ≈ 1 × 10–9 m2/s is molecular diffusion coefficient of component Me in solution; C Me(ss) and C Me(w) ≈ 0 are Me concentrations on sediment surface, i.e., on the bottom boundary of the diffusion water sublayer, and in the water mass, i.e., on the upper boundary of the diffusion water sublayer). The value of depends on water saturation with dissolved oxygen (\({\eta _{{O_2}}}\)) in accordance with the empiric relationship \({C_{Me\left( {ss} \right)}} = \frac{{C_{_{Me\left( {ss} \right)}}^{\max }}}{{1 + k{\eta _{{O_2}}}}}\) (k is a constant factor equal to 300 for iron and 100 for manganese; C Me(ss) max is the maximal concentration of Me on the bottom boundary of the diffusion water sublayer with C Fe(ss) max ≈ 200 μM (11 mg/L), and C Mn(ss) max ≈ 100 μM (5.5 mg/L).  相似文献   

15.
Stable isotope paleoaltimetry has provided unprecedented insights into the topographic histories of many of the world’s highest mountain ranges. However, on the Tibetan Plateau (TP), stable isotopes from paleosols generally yield much higher paleoaltitudes than those based on fossils. It is therefore essential when attempting to interpret accurately this region’s paleoaltitudes that the empirical calibrations of local stable isotopes and the relations between them are established. Additionally, it is vital that careful estimations be made when estimate how different isotopes sourced from different areas may have been influenced by different controls. We present here 29 hydrogen isotopic values for leaf wax-derived n-alkanes (i.e., δDwax values, and abundance-weighted average δD values of C29 and C31) in surface soils, as well as the δD values of soil water (δDsw) samples (totaling 22) from Mount Longmen (LM), on the eastern TP (altitude ~0.8–4.0 km above sea level (asl), a region climatically affected by the East Asian Monsoon (EAM). We compared our results with published data from Mount Gongga (GG). In addition, 47 river water samples, 55 spring water samples, and the daily and monthly summer precipitation records (from May to October, 2015) from two precipitation observation stations were collected along the GG transect for δD analysis. LM soil δDwax values showed regional differences and responded strongly to altitude, varying from?160‰ to?219‰, with an altitudinal lapse rate (ALR) of?18‰ km?1 (R 2=0.83; p<0.0001; n=29). These δDwax values appeared more enriched than those from the GG transect by ~40‰. We found that both the climate and moisture sources led to the differences observed in soil δDwax values between the LM and GG transects. We found that, as a general rule, ε wax/rw, ε wax/p and ε wax/sw values (i.e., the isotopic fractionation of δDwax corresponding to δDrw, δDp and δDsw) increased with increasing altitude along both the LM and GG transects (up to 34‰and 50‰, respectively). Basing its research on a comparative study of δDwax, δDp, δDrw(δDspringw) and δDsw, this paper discusses the effects of moisture recycling, glacier-fed meltwater, relative humidity (RH), evapotranspiration (ET), vegetation cover, latitude, topography and/or other factors on ε wax/p values. Clearly, if ε wax-p values at higher altitudes are calculated using smaller ε wax-p values from lower altitudes, the calculated paleowaterδDp values are going to be more depleted than the actual δD values, and any paleoaltitude would therefore be overestimated.  相似文献   

16.
The hydrogen isotopic composition(δD) of leaf wax long-chain n-alkanes(C27, C29, and C31) from lacustrine sediments has been widely applied to reconstruct terrestrial paleoclimatic and paleohydrological changes. However, few studies have addressed whether the aquatic-derived n-alkanes can affect the δD values of lake sedimentary long-chain n-alkanes, which are usually regarded as a recorder of the terrestrial hydrological signals. Here we systematically investigated δD values of long-chain n-alkanes from modern aquatic plants, both near-shore and off-shore surface sediments, surrounding terrestrial plant litters, as well as river water and lake water in Lake Qinghai and its satellite lakes on the northeastern Qinghai-Tibet Plateau. Our data showed that(i) δD values of long-chain n-alkanes from aquatic plants varied from-184‰ to-132‰ for n-C27, from-183‰ to-138‰ for n-C29, and from-189‰ to-130‰ for n-C31, respectively, with no significant differences among the three n-alkanes homologues;(ii) δD values of long-chain n-alkanes from aquatic plants were generally more positive than those from surrounding terrestrial plants, possibly because that they recorded the D-enrichment of lake water in this semi-arid region;(iii) δD values of long-chain n-alkanes from surface sediments showed significant differences among the three n-alkanes homologues, due to the larger aquatic input of n-C27 to the sedimentary lipid pool than that of n-C31, and(iv) n-C27 δD values of near-shore aquatic plants and near-shore sediments are more negative than those from off-shore as a result of lower δD values of near-shore lake water. Our findings indicate that in this region(i) the offset between sedimentary n-C27 and n-C31 δD values(ΔδDC27-C31) could potentially be used to evaluate if sedimentary long-chain n-alkanes are derived from a single source;(ii) while δD values of n-C27 may be influenced by lake water hydrological changes, sedimentary n-C31 is derived predominantly from terrestrial plants and thus its δD can serve as a relatively reliable indicator for terrestrial paleoclimatic and paleohydrological reconstructions.  相似文献   

17.
The composition characteristics of light hydrocarbons from crude oil, chloroform bitumen A, saturated hydrocarbon fraction, aromatic hydrocarbon fraction, and asphaltene fraction during cracking have been studied systematically. The results revealed that the content of n-alkanes, branched alkanes and cycloalkanes in light hydrocarbons from the samples gradually decreased as the simulation temperature increased, and finally almost depleted completely, while the abundance of methane, benzene and its homologues increased obviously and became the main products. The ratios of benzene/ n-hexane and toluene/n-heptane can be used as measures for oil cracking levels. Variation characteristics of maturity parameters of light hydrocarbons, for example, iC4/nC4, iC5/nC5, isoheptane value, 2,2-DMC4/nC6, and 2-MC6+3-MC6/nC7 for different samples with increasing pyrolysis temperature, are consistent with those in petroleum reservoirs, indicating that these parameters may be efficient maturity index.  相似文献   

18.
A recently proposed model of foam impact on the air–sea drag coefficient C d has been employed for the estimation of the effective foam-bubble radius R b variation with wind speed U10 in hurricane conditions. The model relates C d (U10) with the effective roughness length Z eff (U10) represented as a sum of aerodynamic roughness lengths of the foam-free and foam-covered sea surfaces Z w (U10) and Z f (U10) weighted with the foam coverage coefficient α f (U10). This relation is treated for known phenomenological distributions C d (U10), Z w (U10), and α f (U10) at strong wind speeds as an inverse problem for the effective roughness parameter of foam-covered sea surface Z f (U10). The present study is aimed at the estimation of the effective roughness of the sea surface assuming that the measurement data for the effective drag coefficient are known. The effective foam-bubble size is found as a function of the wind speed.  相似文献   

19.
Recent estimates of fracture energy G ′ in earthquakes show a power-law dependence with slip u which can be summarized as G ′ ∝ u a where a is a positive real slightly larger than one. For cracks with sliding friction, fracture energy can be equated to G f : the post-failure integral of the dynamic weakening curve. If the dominant dissipative process in earthquakes is friction, G ′ and G f should be comparable and show a similar scaling with slip. We test this hypothesis by analyzing experiments performed on various cohesive and non-cohesive rock types, under wet and dry conditions, with imposed deformation typical of seismic slip (normal stress of tens of MPa, target slip velocity > 1 m/s and fast accelerations ≈ 6.5 m/s2). The resulting fracture energy G f is similar to the seismological estimates, with G f and G ′ being comparable over most of the slip range. However, G f appears to saturate after several meters of slip, while in most of the reported earthquake sequences, G ′ appears to increase further and surpasses G f at large magnitudes. We analyze several possible causes of such discrepancy, in particular, additional off-fault damage in large natural earthquakes.  相似文献   

20.
Six species of more than 20-year-old desert woody plants in the oasis-desert ecotone were selected for study. The results showed that: (1) in different growing seasons δ13C values of assimilating organ varied between -14%. and -16%. for Haloxylon ammodendron (HA),-14%. - -15%. for Calligonum mongolicum (CM) and -25%. - -28%. for Caragana korshinskii (CK), Nitraria sphaerocarpa (NS) and Hedysarum scoparium (HS). (2) The net photosynthetic rate (Pn) of HA and CM was significantly higher than those of the other species. With the decrease in Pn for the six species, their intercellular CO2 concentration increased, but stomatal limitation value decreased under the intensive light. At the same time, the photochemical efficiency of PS II dropped to different degrees. (3) The CO2 enrichment experiment demonstrated that, Pn of HA and CM increased to different extent under 450 μmol/mol, but their Pn reduced or approximated to the current condition under 650 μmol/mol. Under 450 μmol/mol the efficiency for solar energy utilization of CK and HS significantly reduced and under 650 μmol/mol their respiration rate exceeded photosynthesis rate. It can be concluded that HA and CM have some function of pathway for C4 but the other three species have the function for C3. The decline in their Pn is mainly caused by non-stomatal factors. HA, CM, CK and HS exhibited photoinhibition, which disappeared in a short time. This is a kind of positive readjustment to adapting to the desert environment. HA and CM can adapt to the high CO2 environment, but CK and HS cannot. With the rise in atmospheric CO2 concentration and climate warming, the latter two species in the oasis-desert ecotone may be gradually degraded or even disappear.  相似文献   

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