Ore fluid of the Tieluping silver deposit of Henan Province and its illustration of the tectonic model for collisional petrogenesis,metallogenesis and fluidization

The Tieluping silver deposit, located in the NE-trending faults within the metamorphic basement of the Xiong'er Mountain, is a typical altered fracture type deposit. Its ore-forming process includes three stages with temperatures concentrated at 373°C, 223°C and 165°C respectively. With δD=90‰,\(\delta ^{13} C_{CO_2 } \)=2.0‰ and δ{si18}O=8094‰, the early stage fluid was generated from reworking and metamorphism of the carbonate rich formation; the late one, with δD=?70‰,\(\delta ^{13} C_{CO_2 } \)=-1.2‰, δ¹⁸O=1.89‰, was meteoric hydrothermal solution; and the middle. δD=?109‰,\(\delta ^{13} C_{CO_2 } \)=0.1‰, δ¹⁸O=1.79‰, might be a hybrid mixed by reworking-metamorphic fluid and meteoric hydrothermal solution. Crystallized rapidly in the condition of fluid-boiling and fluid-mixing, the middle stage minerals have far more fluid inclusions with higher content of ions, higher ratios of H₂O/CO₂ and KN/MC. Consequently, they have much more ore elements such as gold compared with those of the early and late stages. It was the northward intracontinental subduction along the Machaoying fault during the Mesozoic collision between the South China and North China paleocontinents that intrigued large-scale fluidization and magmatism and led to the appearance of more than 10 large and medium hydrothermal deposits, including the Tieluping silver deposit. The study on ore-forming fluidization of the Tieluping silver deposit proves the CPMF model.     

Evaluation of the carbon isotopic effects of NDIR and CRDS analyzers on atmospheric CO2 measurements

Non-dispersive infrared(NDIR) and cavity ring-down spectroscopy(CRDS) CO_2 analyzers use 12CO_2 isotopologue absorption lines and are insensitive to all or part of other CO_2-related isotopologues. This may produce biases in CO_2 mole fraction measurements of a sample if its carbon isotopic composition deviates from that of the standard gases being used. To evaluate and compare the effects of carbon isotopic composition on NDIR and CRDS CO_2 analyzers, we prepared three test sample air cylinders with varying carbon isotopic abundances and calibrated them against five standard cylinders with ambient carbon isotopic composition using CRDS and NDIR systems. We found that the CO_2 mole fractions of the sample cylinders measured by G1301(CRDS) were in good agreement with those measured by Lo Flo(NDIR). The CO_2 values measured by both instruments were higher than that of a CO_2 isotope measured by G2201i(CRDS) analyzer for a test cylinder with depleted carbon isotopic composition δ~(13)C =-36.828‰, whereas no obvious difference was found for other two test cylinders with δ~(13)C=-8.630‰ and δ~(13)C=-15.380‰, respectively. According to the theoretical and experimental results, we concluded that the total CO_2 mole fractions of samples with depleted isotopic compositions can be corrected on the basis of their 12CO_2 values calibrated by standard gases using Lo Flo and G1301 if the δ~(13)C and δ18O values are known.     

Ore fluid of the Tieluping silver deposit of Henan Province and its illustration of the tectonic model for collisional petrogenesis,metallogenesis and fluidization

The Tieluping silver deposit, located in the NE-trending faults within the metamorphic basement of the Xiong'er Mountain, is a typical altered fracture type deposit. Its ore-forming process includes three stages with temperatures concentrated at 373°C, 223°C and 165°C respectively. With δD=90‰,\(\delta ^{13} C_{CO_2 } \)=2.0‰ and δ{si18}O=8094‰, the early stage fluid was generated from reworking and metamorphism of the carbonate rich formation; the late one, with δD=−70‰,\(\delta ^{13} C_{CO_2 } \)=-1.2‰, δ¹⁸O=1.89‰, was meteoric hydrothermal solution; and the middle. δD=−109‰,\(\delta ^{13} C_{CO_2 } \)=0.1‰, δ¹⁸O=1.79‰, might be a hybrid mixed by reworking-metamorphic fluid and meteoric hydrothermal solution. Crystallized rapidly in the condition of fluid-boiling and fluid-mixing, the middle stage minerals have far more fluid inclusions with higher content of ions, higher ratios of H₂O/CO₂ and KN/MC. Consequently, they have much more ore elements such as gold compared with those of the early and late stages. It was the northward intracontinental subduction along the Machaoying fault during the Mesozoic collision between the South China and North China paleocontinents that intrigued large-scale fluidization and magmatism and led to the appearance of more than 10 large and medium hydrothermal deposits, including the Tieluping silver deposit. The study on ore-forming fluidization of the Tieluping silver deposit proves the CPMF model.

     

Influence of aquatic plants on the hydrogen isotope composition of sedimentary long-chain n-alkanes in the Lake Qinghai region,Qinghai-Tibet Plateau

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.     

Preliminary study on the origin identification of natural gas by the parameters of light hydrocarbon

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 ¹³C_benzene> ?24‰, δ ¹³C_toluene >?23‰, δ ¹³C_cyclohexane > ?24‰ and δ ¹³C_{methyl cyclohexane}> ?24‰, while the sapropelic-sourced gas has the distribution of δ ¹³C_benzene <?24‰, δ ¹³C_toluene< ?24‰, δ ¹³C_cyclohexane< ?24‰ and δ ¹³C_{methyl 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 C_5–7 aliphatics, the gas with relative content of C_5–7 normal alkane of more than 30% is sapropelic-sourced gas, while the gas with relative content of C_5–7 normal alkane of less than 30% is humic-sourced gas. These paremeters have been suggested to identify humic-sourced gas and sapropelic-sourced gas.     

The distribution characteristic and its significance of compound specific isotopic composition of aromatic hydrocarbon from marine source rock and oil in the Tarim Basin,western China

Aromatic hydrocarbons are generally main distillation of crude oil and organic extract of source rocks. Bicyclic and tricyclic aromatic hydrocarbons can be purified by two-step method of chromatography on alumina. Carbon isotopic composition of individual aromatic hydrocarbons is affected not only by thermal maturity, but also by organic matter input, depositional environment, and hydrocarbon generation process based on the GC-IRMS analysis of Upper Ordovician, Lower Ordovician, and Cambrian source rocks in different areas in the Tarim Basin, western China. The subgroups of aromatic hydrocarbons as well as individual aromatic compound, such as 1-MP, 9-MP, and 2,6-DMP from Cambrian-Lower Ordovician section show more depleted 13 C distribution. The 13 C value difference between Cambrian-Lower Ordovician section and Upper Ordovician source rocks is up to 16.1‰ for subgroups and 14‰ for individual compounds. It can provide strong evidence for oil source correlation by combing the 13 C value and biomarker distribution of different oil and source rocks from different strata in the Tarim Basin. Most oils from Tazhong area have geochemical characteristics such as more negative 13C9-MP value, poor gammacerane, and abundant homohopanes, which indicate that Upper Ordovician source rock is the main source rock. In contrast, oils from Tadong area and some oils from Tazhong area have geochemical characteristics such as high 13C9-MP value, abundant gammacerane, and poor homohopanes, which suggest that the major contributor is Cambrian-Lower Ordovician source rock.     

Hard X-ray generation in the turbulent plasma of solar flares

The influence of scattering of accelerated electrons in the turbulent plasma on the transformation of their distribution function is studied. The turbulence is connected with the emergence of magnetic inhomogeneities and ion-sound mode. The level of ion-sound turbulence is specified by the ratio W ^s/nk _B T _e = 10^?3, while the value of magnetic fluctuations is δB/B = 10^–3. Different initial angular distributions of the function of accelerated-electron source are regarded: from isotropic to narrow directional distributions. For the chosen energy-density values of the ion-sound turbulence and the level of magnetic fluctuations, it is shown that both types of turbulence lead to a qualitative change in the hard X-ray brightness along the loop, moreover their influence was found to be different. Models with magnetic fluctuations and the ion sound can be distinguished not only by the difference in the hard X-ray distribution along the loop but also by the photon spectrum.     

On the timing of the East Asian summer monsoon maximum during the Holocene—Does the speleothem oxygen isotope record reflect monsoon rainfall variability?

The evolution of the East Asian summer monsoon(EASM) during the Holocene has long been of significant interest.Knowledge of past EASM variability not only increases our understanding of monsoon dynamics on a long timescale,but it also provides an environmental and climatic background for research into Chinese cultural development.However,the timing of the EASM maximum remains controversial.The popular concept of an "early Holocene maximum" is mainly based on speleothemδ~(18)O(δ~(18)O_c) records from caves in southern China;however,the interpretation of δ~(18)O_C as a reliable proxy for EASM intensity is being increasingly challenged.The present paper is a critical review of the climatic significance of the δ~(18)O_C record from China.Firstly,we suggest that precipitation in northern China is an appropriate index of EASM intensity,the variation of which clearly indicates a mid-Holocene monsoon maximum.Secondly,an interregional comparison demonstrates that the precipitation record in northern China is quite different from that in southern China on a range of timescales,and is inconsistent with the spatial similarity exhibited by speleothem oxygen isotope records.Furthermore,both modeling and observational data show that the δ~(18)O_C records from southern China indeed reflect changes in precipitation δ~(18)O(δ~(18)O_P) rather than precipitation amount,and therefore that their use as an EASM proxy is inappropriate.Finally,we address several significant monsoon-related issues-including the driving mechanism of the EASM on an orbital timescale,the climatic significance of speleothem oxygen isotopes,and the relationship between atmospheric circulation and precipitation in monsoonal regions.     

Characterization of the Tail of the Distribution of Earthquake Magnitudes by Combining the GEV and GPD Descriptions of Extreme Value Theory

The present work is a continuation and improvement of the method suggested in Pisarenko et al. (Pure Appl Geophys 165:1–42, 2008) for the statistical estimation of the tail of the distribution of earthquake sizes. The chief innovation is to combine the two main limit theorems of Extreme Value Theory (EVT) that allow us to derive the distribution of T-maxima (maximum magnitude occurring in sequential time intervals of duration T) for arbitrary T. This distribution enables one to derive any desired statistical characteristic of the future T-maximum. We propose a method for the estimation of the unknown parameters involved in the two limit theorems corresponding to the Generalized Extreme Value distribution (GEV) and to the Generalized Pareto Distribution (GPD). We establish the direct relations between the parameters of these distributions, which permit to evaluate the distribution of the T-maxima for arbitrary T. The duality between the GEV and GPD provides a new way to check the consistency of the estimation of the tail characteristics of the distribution of earthquake magnitudes for earthquake occurring over an arbitrary time interval. We develop several procedures and check points to decrease the scatter of the estimates and to verify their consistency. We test our full procedure on the global Harvard catalog (1977–2006) and on the Fennoscandia catalog (1900–2005). For the global catalog, we obtain the following estimates: \( \hat{M}_{{\rm max} } \)  = 9.53 ± 0.52 and \( \hat{Q}_{10} (0.97) \)  = 9.21 ± 0.20. For Fennoscandia, we obtain \( \hat{M}_{{\rm max} } \)  = 5.76 ± 0.165 and \( \hat{Q}_{10} (0.97) \)  = 5.44 ± 0.073. The estimates of all related parameters for the GEV and GPD, including the most important form parameter, are also provided. We demonstrate again the absence of robustness of the generally accepted parameter characterizing the tail of the magnitude-frequency law, the maximum possible magnitude M _max, and study the more stable parameter Q _T (q), defined as the q-quantile of the distribution of T-maxima on a future interval of duration T.     

Altitudinal effect of soil <Emphasis Type="Italic">n</Emphasis>-alkane <Emphasis Type="Italic">δ</Emphasis>D values on the eastern Tibetan Plateau and their increasing isotopic fractionation with altitude

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., _δD_wax values, and abundance-weighted average δD values of C₂₉ and C₃₁) in surface soils, as well as the δD values of soil water (δD_sw) 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 _δD_wax 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 _δD_wax 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 _δD_wax 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 _δD_wax corresponding to δD_rw, δD_p and δD_sw) 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 _δD_wax, δD_p, δD_rw(δD_springw) and δD_sw, 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 paleowaterδD_p values are going to be more depleted than the actual δD values, and any paleoaltitude would therefore be overestimated.     

Modeling of Physical Processes by Analysis of Hard X-Ray and Microwave Radiations in the Solar Flare of November 10, 2002

For electron acceleration during solar flares, it is very important to determine the pitch-angle and energy dependences of the electron distribution function. At present, this cannot be done directly from observations. Therefore, it is necessary to perform a numerical simulation of the propagation of accelerated electrons in the magnetic field of the flare loop (loops) and calculate the X-ray and radio emissions. For the solar flare of November 10, 2002, we have obtained qualitative and quantitative agreements of modeled X-ray and radio maps with the RHESSI satellite and Nobeyama Radioheliograph data. We have determined the flare model parameters that agree with observations. The pitch-angle anisotropy of electrons determined by highly directional functions of the S(α) = cos⁸(α) type, the energy spectrum consist of two electron populations, the low-energy part of the spectrum up to an energy of break of 350 keV is characterized by a power law with the exponent δ₁ = 2.7–2.9, and the energy spectrum is more rigid above 420 keV (δ₂ = 2–2.3).     

The linear relation between temperatures based on the silica content of groundwater and regional heat flow: A new heat flow map of the United States

Application of the silica geothermometer to over 70,000 non-thermal groundwaters from the United States has shown that there is a correlation between the average silica geotemperatures for a region (T SiO₂ in °C) and the known regional heat flow (q in mW m^?2) of the form: 1 $$TSiO_2 = mq + b$$ wherem andb are constants determined to be 0.67°C m² mW^?1 and 13.2°C respectively. The physical significance of ‘b’ is the mean annual air temperature. The slope ‘m’ is related to the minimum average depth to which the groundwaters may circulate. This minimum depth is estimated to be between 1.4 and 2.0 km depending on the rock type. A preliminary heat flow map based on equation (1) is presented using theT SiO₂ for new estimates of regional heat flow where conventional data are lacking. Anomalously high localT SiO₂ values indicate potential geothermal areas.     

Volcan ceboruco: A major composite volcano of the mexican volcanic belt

Ceboruco is a major composite volcano at the western end of the Mexican Volcanic Belt, near the junction between the North American and Pacific plates. The volcano is built from successive eruptions of andesite lavas and pyroclastic rocks, and major eruptions during its history have resulted in the formation of two concentric calderas. The youngest volcanic activity has included the extrusion of dacites within the inner caldera and a voluminous flank eruption of andesite during 1870–72. Fumarolic activity persists to the present day. Chemical analyses show that the lavas are of cale-alkaline type and rangs from andesite (SiO₂=58–61%) to acid dacite (SiO₂=68%) in composition. The rate of increase of K₂O relative to SiO is greater than that in volcanic rocks from the Mexican Volcanic Belt as a whole. This indicates that simple models based on the application of such relationships may not be adequate to explain the petrogenesis of calc-alkaline lavas.     

Geochemical characteristics and origin of gases from the Upper,Lower Paleozoic and the Mesozoic reservoirs in the Ordos Basin,China

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.     

Stable isotopic compositions and controlling factors of precipitation and atmospheric vapour in the headwaters of the Shule River

Stable isotopic compositions of precipitation (δ¹⁸O_p, δ²H_p and d-excess_p) and atmospheric vapour (δ¹⁸O_v, δ²H_v and d-excess_v) with high spatial–temporal resolution are crucial in revealing hydrologic cycle. Based on the variation characteristics of δ¹⁸O_p/δ¹⁸O_v, δ²H_p/δ²H_v and d-excess_p/d-excess_v in the headwaters of the Shule River (HSR) on hourly and daily scales from June to September 2018, this study analysed the relationships between δ¹⁸O_p/δ²H_p and δ¹⁸O_v/δ²H_v combined with the equilibrium fractionation model, as well as δ¹⁸O_p/δ¹⁸O_v and meteorological factors. The slopes of local meteoric water line (LMWL) and the δ²H_v-δ¹⁸O_v fitting equation were similar (7.96 and 7.94) with both intercepts exceeding 10, reflecting the great contribution of recycling moisture. The values of δ¹⁸O_v/δ²H_v were lower than δ¹⁸O_p/δ²H_p but with consistent variation patterns throughout the period. The equilibrium simulation results suggested that precipitation and atmospheric vapour almost approached isotopic equilibrium state, especially during monsoon intrusion period. Affected by monsoon intrusion, the slopes and intercepts of the LMWLs and the δ²H_v-δ¹⁸O_v fitting equations were smaller than those during non-monsoon period and d-excess and δ¹⁸O were negatively correlated. Relative humidity had significant negative correlations with δ¹⁸O_p and δ¹⁸O_v in the whole period, however, the positive correlations between δ¹⁸O_p/δ¹⁸O_v and temperature were observed during non-monsoon and monsoon intrusion period, respectively. Our results demonstrated that precipitation and atmospheric vapour isotopic compositions exhibited consistency under the influence of diverse moisture sources, while more complex relationships were found between δ¹⁸O_p/δ¹⁸O_v and meteorological factors. This research provided evidence for using the isotopic compositions of atmospheric vapour to indicate moisture sources, and can improve understanding of the water cycle and eco-hydrological process from the perspective of the interaction between water and gas phases of the inland river basin in northwest China.     

Geochemical characteristics of pyrolysis gas from epimetamorphic rocks in the northern basement of Songliao Basin,Northeast China

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.     

Major-element petrochemistry of some extrusive rocks from the volcanically active Mariana Islands

Volcanic rocks from six of the currently or recently active volcances of the Mariana Island are show little variation in major element abundances. SiO₂ content averages 51.5 wt.%. The flows are high in Al₂O (mean 17.7 wt.%) and Fe oxides (mean 10.1 wt.% calculated as FeO only), and moderate in MgO content (mean 4.7 wt.%), Na₂O (mean 2.7 wt.%), and K₂O (mean 0.7 wt.%). Only the rocks from Farallon de Pajaros, the northernmost of the Mariana Islands, deviate slightly from the average of the analyses. Three analyses from this island are slightly higher in SiO₂ (about 54 wt.%) and Al₂O₃, and are lower in total Fe oxides and MgO. According to preferred classification, the lavas of the Mariana Islands can be termed mela-andesites, high-alumina basalts, or calc-alkaline (orogenic) basalts. The K₂O values (mean 0.7 wt.%) obtained from lavas of the Mariana Islands are significantly higher than the K₂O values (about 0.33 wt.%) from volcanics of the Izu chain to the north. Inasmuch as the substantial scatter in location of earthquake foci beneath both arcs prevents accurate delineation of the upper boundary of the Benioff zone, it presently cannot be determined whether this discrepancy in K₂O values reflects a difference in depth from the volcanic are to the dipping seismic zone or relates to other phenomena. The older volcanic islands within the Mariana-Bonin island chain apparently defined an island arc system during Eocene to Miocene time. This indicates that the present plane of convergence between the Pacific plate and the Philippine Sea plate has defined the convergence between these plates since Eocene time.     

Catchment environmental change over the 20th Century recorded by sedimentary leaf wax n-alkane δ~(13)C off the Pearl River estuary

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.     

Characterization of the negative carbon isotope shift in segment C2, its global implications as a harbinger of OAE1a

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 ¹³C_org and δ ¹³C_carb 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 ¹³C_org, 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.