Determination of Hf–Sr–Nd isotopic ratios by MC-ICP-MS using rapid acid digestion after flux-free fusion in geological materials

In this study, we established a rapid acid digestion for determining Hf-Sr-Nd isotopic ratios of geological samples by using MC-ICP-MS. Conditions of 1600 ℃ for 1 min and 1400 ℃ for 1 min were adopted for fusing intrusive rocks and extrusive rocks, respectively. The rapid acid digestion technique is superior in digestion time compared with high-pressure PTFE bomb method. The procedural blanks of the method were also lower than that flux fusion. Replicate analyses of international certified reference materials （CRMs） indicate that isotopic ratios of ^176Hf/^177Hf, ^87Sr/^86Sr and 143Nd/144Nd agree well with previously published data. The external reproducibility （2SD, n = 5） of ten CRMs are ±0.000030 for ^87Sr/^86Sr, ± 0.000030 for ^143Nd/^144Nd, and ±0.000018 for ^176Hf/^177Hf.

Petrogenesis of Indosinian Granitoids in Middle-Segment of South Qinling Tectonic Belt:Constraints from Sr-Nd Isotopic Systematics

South Qinling Tectonic Belt（SQTB）is located between the Shangzhou-Danfeng and Mianxian-Lueyang sutures.There are a lot of early Mesozoic granitoid plutons in its middle segment, comprising the Dongjiangkou-Zhashui granitoid plutons at the northeast,Huayang-Wulong-Laocheng granitoid plutons at the central part,Xiba granitoid pluton at the northwest and Guangtoushan-Liuba granitoid plutons at the southwest.These Indonisian granitoids contain a mass of various scale mafic enclaves,which show sometimes clear boundaries and sometimes transitional boundaries with their host granitoids.These granitoids also exhibit metaluminous to peraluminous series,commonly higher Mg# and a wide range of petrochemistry from low-K tholeiite series,through mid-K and high-K calc-alkaline series to shoshonite series and predominated samples are attributed to mid-K and high-K calc-alkaline series.Detailed analyses in Sr-Nd isotopic systematics and petrochemistry reveal that there may be regionally initial granitoid magma of the Indonisian granitoid plutons,comprising Dongjiangkou-Zhashui,Huayang-Wulong-Laocheng,Xiba,and Guangtoushan-Liuba granitoid plutons,which were produced by hybrids of magmas in various degrees,and the initial magmas were derived from both the mantle and the lower continental crust（LCC）sources in the SQTB.The initial granitoid magma further did the magma hybrid with the magmas from the LCC,crystallization fractionation,and assimilation with upper crustal materials during their emplacement to produce these granitoid plutons in the SQTB.These magmatism processes are most likely to occur under continent marginal arc and syn-collision to post-collision tectonic backgrounds.

Geochemistry,Geochronology,Sr-Nd Isotopic Compositions of Jiang Tso Ophiolite in the Middle Segment of the Bangong- Nujiang Suture Zone and Their Geological Significance

The Jiang Tso ophiolite, situated in the middle segment of the Bangong- Nujiang Suture Zone, is a part of the easternmost Qieli Lake ophiolite subzone and is close to the south of Pung Lake ophiolite. The rock association of Jiang Tso ophiolite is relatively complete and is mainly composed of metamorphic peridotite, gabbro and diabase. Comparing with N-MORB, the ophiolite is high in Mg and low in Ti, K, Na, P, and is depleted in Nb, Ta, Hf, Th and enriched in Rb, Sr and Ba. Geochemical characteristics of the Jiang Tso ophiolite indicate it is of a supra-subduction zone type formed in the spreading ridge of back arc basin. The SHRIMP U-Pb dating of zircons from the gabbro yielded a weighted average age of 188.1±4.1 Ma （MSWD=1.4）, indicating the Jiang Tso ophiolite was formed in the late stage of early Jurassic. The Sr, Nd isotopic compositions show that the Tethyan mantle domain is the depleted mantle （DM）, with enriched mantle domain II （EMII）. They have the same Sr, Nd isotopic composition with the India Ocean MORB type.

Delineating the Source of Lead in the Urban Atmospheric Dust Based on Stable Isotopic Ratio: A Case Study from Panzhihua City of Southwest China

Atmospheric lead pollution is a global problem.Mining,coal mining,iron and steel smelting,and chemical and coal-fired power plants are major industries in Panzhihua City of southwest China.Many toxic and harmful heavy metals,including Pb,are emitted in production activities.Pb seriously affects human health and natural ecosystems.Thus,Pb source tracing is important for Pb pollution control(Souto-Oliveira et al.,2018;Zhao et al.,2015).

Petrogenesis and Tectonic Implications of A-type Granites in Zhaheba in the East Junggar Region of Xinjiang,China:Evidence from Geochronology,Geochemistry and Sr-Nd Isotopic Compositions

The magma source,petrogenesis,tectonic setting and geochronology of the late Paleozoic A-type granites widely exposed in the Zhaheba area,East Junggar,have thus far not been well-constrained.A better understanding of these issues will help to reveal the magmatic processes and continental growth of Central Asia.The A-type granites in Zhaheba include the Ashutasi alkaline granites and the Yuyitasi syenogranites,which were emplaced at 321.5±4.8 Ma and 321.7±0.6 Ma,respectively.The major rock-forming minerals are orthoclase,perthite,arfvedsonite and quartz,which exhibit the following principal geochemical characteristics of A2-type granites.(1)Their REE distribution curves each exhibit a‘V’-shaped pattern and a marked depletion in Eu.They are rich in large-ion lithophile elements Rb,Th and U as well as high-field-strength elements Nb,Ta,Zr and Hf,but significantly depleted in Ba,Sr,P and Ti.(2)Their(^(87)Sr/^(86)Sr)i values(0.7021-0.7041),εNd(t)values(4.57-5.16)and REE distribution patterns are in basic agreement with those of the Kalamaili A-type granite belt in East Junggar.The T DM2 values of the alkaline granites and syenogranites range from 661 to 709 Ma.The A-type granites may be the products of upwelling asthenosphere-triggered partial melting of immature lower crust.The alkaline granites were late-stage products of crystallization and differentiation.Compared to the syenogranites,the alkaline granites are significantly lower in K_(2)O,Na_(2)O,Al_(2)O 3,FeO,MgO and CaO,but significantly higher in incompatible elements(e.g.,SiO_(2),Rb,and Sr).The magmatic crystallization temperatures of the syenogranites and alkaline granites are 874℃ and 819℃,respectively.As their age gradually decreases(peak ages:322 Ma and 307 Ma,respectively),there is a gradual decrease in the T_(DM2)of the A-type granites and a gradual increase in theεNd(t)value from the Ulungur belt to the Kalamaili belt in East Junggar.The study of A-type granites is therefore one of the keys to understanding the laws and mechanisms of crustal accretion during the Phanerozoic period,as well as also being of great significance for understanding the Paleozoic accretion.

CAUBRATION METHOD IN ISOTOPIC CARBON ANALYSIS

A very simple basic equation for the comparator technique is derived for the determination of 13C/12C ratio in biological samples by proton induced gamma- ray emission. On the basis of this treatments a new series of experiments has been made at a 2×1.7 tandem accelerator that proved conclusion about the method.

Genesis of A-type Granites in the East Junggar, Xinjiang and Growth of Continental Crust——Evidence from Geochronological and Sr-Nd Isotopic Compositions

The magma source,petrogenesis,tectonic setting and its geochronology of the Late Paleozoic A-type granites,which widely exposed in Zhaheba area,East Junggar,have not been well constrained so far(Fig.1 a,b).A better understanding of above issues will help us to reveal the magmatic processes and the continental growth of Central Asia(Xiao et al.,2009).

DOUBLE SUBSTITUTE CALIBRATION FOR THE ISOTOPIC RATIO MEASUREMENT AMONG RARE EARTH ELEMENTS

Abstract: Through the application of the method of double substitute calibration using the true isotopic ratios of cerium and europium of our laboratory standards, the atomic weight of ytterbium has been determined as Ac(Yb) 173. 0428(15) on Zσ basis.

Mafic Dyke Records of Paleoproterozoic Mantle Plume Activity in the Karelian Craton: U-Pb Baddeleyite/Zircon Geochronology and Sr-Nd Isotopic Data

Mafic dykes preserved important information on mantle melting regimes in the early Earth history.Despite the fact that a large volume of geochronological data for mafic dykes was recently received,several important issues

Pb concentrations and isotopic compositions in the soil and sediments around the abandoned mine in southwest of Korea

This study was undertaken to investigate the influence of Pb contaminant dispersal from an abandoned mine. For the study, 23 samples of sediment and soil were collected around the abandoned mine located in southwest of Korea. Pb concentrations and isotope ratios of sediment samples were analyzed through ICP-OES (Optima 5300 DV, Perkin Elmer) and MC-ICP-MS (Plasma II, Nu), respectively. The sediment samples collected in the main stream from the mine entrance showed high Pb concentrations of 139 - 1079 mg/kg, while Pb concentrations of the other sites were 19 - 29 mg/kg. Pb isotope ratios of the main stream sediments were 2.4854 - 2.4883 for 208Pb/207Pb and 1.1693 - 1.1740 for 206Pb/207Pb. On the other hand, the Pb isotopic compositions of sediments collected from the other sites were clearly different from those of ore deposits. The Pb isotope ratios versus inverse concentrations plot showed high linear correlation between the main stream, the tributary stream and one of the downstream sites representing the two end member mixing system between these sites. According to the binary mixing equation, the relative contribution of Pb pollutants from the abandoned mine to the downstream area were approximately 33% - 36%.

Oxygen Stable Isotopic Ratio in Precipitations in Niigata Prefecture, Japan

Time-course of oxygen stable isotopic ratios （i.e., δ^18O） as well as seasonal variation of δ^18O has been examined to investigate the characteristics, sources and the passing route of precipitations in Niigata Prefecture. The precipitation samples have been mainly collected with a filtrating bulk sampler at the rooftop of Niigata University. Furthermore, backward trajectories analyses have been also conducted for these samples taken sequentially for a short period. Consequently, the following features have been mainly clarified for the precipitations in Niigata Prefecture： （1） the δ^18O values varied between -14.57%o and -3.86%0 in the precipitations of Niigata University; （2） as for the comparison among sampling points, the mean value of δ^18O at seaside spots （i.e., Niigata City： -6.93%0） is larger than that of inland spots （Sanjyo City： -8.68%0）; （3） δ^18O value was generally small in the rainy or typhoon season, and relatively large in summer; （4） decreasing δ^18O content with time is a predominant feature of sequentially sampled rainfalls as predicted by Rayleigh models of atmospheric vapor condensation.

Petrogenesis of high-Mg# Cenozoic volcanic rocks of southern Qiangtang area, Tibetan Plateau： geochemical and Sr-Nd isotopic evidence

The Nadingcuo volcanic rock suite is the most volmninous Cenozoic volcanic suite in the southern Qiangtang area of the northern Tibetan Plateau. These high-K calc-alkaline volcanic rocks were formed between 36 and 34 Ma, characterized by high Mg# values, high concentrations of TiO2 and P205, 87Sr/S6Sr ratios of 0. 704682--0. 706 112, and aNd（t） values of - 1.2 to 1.6. There is a lack of reasonable explanations for sour- cing and origin of magmas that formed the rocks with high Mg# values and TiO2 and P2O5 enrichments, which makes the previous research results still controversial. This study reviews the geochemical characteristics of Nadingcuo volcanic rocks and the data we have newly found in our fieldwork. We give some new interpretation to the magmatic evolution of the basaltic magmas in the discussed area dominated by fractional crystallization. The geochemistry of trachyandesite and trachyte units in the studied area is indicative of formation from mantle- derived magmas that mixed with crustal materials. The high values of Mg# and TiO2 and P205 enrichment in these units are evident to show the mixing between mantle-derived magmas with -30-40 wt.% rhyolitic melt or assimilation of a similar amount of felsic rocks. The geochemistry of basaltic rocks in the area also suggests that the Nadingcuo basalts may have been derived from an ocean island basalt （OIB） -type source that contained and was mixed with ancient mantle wedge derived material, indicating that a 36-34 Ma asthenospheric upwelling e- vent in the Qiangtang area may relate to the northward subduction of Indian lithospheric mantle and the south- ward subduction of Asian lithospherie mantle. This upwelling of asthenospherie material was centered in the southern Qiangtang area between 36 and 34 Ma, while the northward movement of the Indian Craton caused this upwelling mantle flow to continuously migrate northward, resulting in the current centering of this upwelling in the Hoh Xil-Kunlun region.

Crustal Composition of China Continent Constrained from Heat Flow Data and Helium Isotope Ratio of Underground Fluid

Based on conservation of energy principle and heat flow data in China continent, the upper limit of 1.3 μW/m3 heat production is obtained for continental crust in China. Furthermore, using the data of heat flow and helium isotope ratio of underground fluid, the heat productions of different tectonic units in China continent are estimated in range of 0.58-1.12 μW/m3 with a median of 0.85 μW/m3. Accordingly, the contents of U, Th and K20 in China crust are in ranges of 0.83-1.76 μg/g, 3.16-6.69 μg/g, and 1.0%-2.12%, respectively. These results indicate that the abundance of radioactive elements in the crust of China continent is much higher than that of Archean crust; and this fact implies China＇s continental crust is much evolved in chemical composition. Meanwhile, significant lateral variation of crustal composition is also exhibited among different tectonic units in China continent. The crust of eastern China is much enriched in incompatible elements such as U, Th and K than that of western China; and the crust of orogenic belts is more enriched than that of platform regions. It can also be inferred that the crusts of eastern China and orogenic belts are much felsic than those of western China and platform regions, respectively, derived from the positive correlation between the heat production and SiO2 content of bulk crust. This deduction is consistent with the results derived from the crustal seismic velocity data in China. According to the facts of the lower seismic velocity of China than the average value of global crust, and the higher heat production of China continent compared with global crust composition models published by previous studies, it is deduced that the average composition models of global continent crust by Rudnick and Fountain （1995）, Rudnick and Gao （2003）, Weaver and Tarney （1984）, Shaw et al. （1986）, and Wedepohl （1995） overestimate the abundance of incompatible elements such as U, Th and K of continental crust.

Geochemistry of trace elements and Sr-Nd isotopes of foraminifera shell from the Okinawa Trough

Trace elemental associations and Sr-Nd isotopic compositions are of important to recognition of biogenic material from mixed marine sediments. The foraminifera shell from the Okinawa Trough strongly enriches Sr,P,Mn and Ba, enriches Li,U,Th,Sc,Co,Cu,Pb,Zn,Cr,Rb,Y,Sb and light rare earth elements,slightly enriches V,Ga,Zr,Nb,Cd and middle rare earth elements,is short of Mo,In,Sn,Cs,Hf,Ta,W,Ti,Bi and heavy rare earth elements. The mechanism of elemental enrichment in forminifera is the concentrations of trace elements in sea water and selective absorption of trace elements during foraminifera living, as well as the geochemical affinity between major elements and trace elements.The REE (rare earth elements)partition pattern of foraminifera shell of the Okinawa Trough shows enrichment of middle rare earth elements with slightly negative Ce anomaly,which are different from those of foraminifera of the Pacific Ocean.The Sr,Nd isotopic ratios of the Okinawa Trough foraminifera are 0 709 769 and 0 512 162,respectively, which are different not only from those of oceanic water, but also from those of river water of China's Mainland, the former is slightly higher than those of oceanic water,but much lower than those of river water;the latter is slightly lower than those of oceanic water,but higher than those of river water,demonstrating that the Okinawa Trough sea water has been influenced by river water of China's Mainland.

Multi-collector ICP-MS Analysis of Pb Isotope Ratios in Rocks: Data, Procedure and Caution

The authors measured Pb isotope compositions of seven USGS rock referencestandards, i.e. AGV-1, AGV-2, BHVO-1, BHVO-2, BCR-2, BIR-1/1 and W-2, together with NBS 981 using amicromass isoprobe multi-collector inductively-coupled plasma mass spectrometer (MC-ICP-MS) at theUniversity of Queensland. ^(203)Tl-^(205)Tl isotopes were used as an internal standard to correctfor mass-dependant isotopic fractionation. The results for both NBS 981 and USGS rock standardsAGV-1 and BHVO-1 are comparable to or better than double- and triple-spike TIMS (thermal ionizationmass spectrometry) data in precision. The data for BHVO-2 and, to a lesser extent, AGV-2 and BCR-2are reproducibly higher for ^(206)Pb/^(204)Pb, ^(207)Pb/^(204)Pb and ^(208)Pb/^(204)Pb thandouble-spike TIMS data in the literature. The authors also obtained the Pb isotope data for BIR- 1/1and W-2, which may be used as reference values in future studies. It is found that linearcorrection for Pb isotopic fractionation is adequate with the results identical to those correctedfollowing an exponential law or a power law. Precise ^(207)Pb/^(206)Pb, ^(208)Pb/^(206)Pb and^(208)Pb/^(207)Pb ratios can be acquired for sample solutions with Pb>=1 ppb. However, Pb isotoperatios involving ^(204)Pb (i.e., ^(206)Pb/^(204)Pb, ^(207)Pb/^(204)Pb and ^(208)Pb/^(204)Pb) arereliable for solutions with Pb>=40 ppb. The errors for Pb isotope ratio analysis using the MC-ICP-MSare dominated by errors in the analysis of ^(204)Pb, which is commonly ascribed to the difficultyand imprecise correction for a ^(204)Hg isobaric interference. It is found however that the majorerrors on ^(204)Pb come from the tailings of mass ^(203)Tl and mass ^(205)Tl These mass tailingslead to over-subtraction of the baseline for ^(204)Pb, which is measured at +-0.5 amu on both sidesof mass-204 (i.e., at amu 203.5 and 204.5 respectively). Such errors are insignificant for Pb-richsample solutions (i.e., high Pb/Tl ratios), but can be severe for low-Pb sample solutions whenover-'spiked' with Tl. Experiments in this study suggest that a minimum concentration ratio ofPb/Tl>5 in Tl-'spiked' solutions be required to ensure reliable ^(206)Pb/^(204)Pb, ^(207)Pb/^(204)Pband ^(208)Pb/^(204)Pb isotopic ratios. The tailings of ^(203)Tl and ^(205)Tl can also lead toover-subtraction of baselines for ^(202)Hg (at amu 202.5) and ^(206)Pb (at amu 205.5). Therefore,the elegance of using ^(203)Tl and ^(205)Tl isotopes for mass fractionation correction becomes asevere problem in low-Pb rock solution-caution is required. Alternative internal standards for massfractionation correction may be considered. Of course, significant instrumental refinement inabundance sensitivity is in demand.

An online method to determine chlorine stable isotope composition by continuous flow isotope ratio mass spectrometry (CF-IRMS) coupled with a Gasbench Ⅱ

An online method using continuous flow isotope ratio mass spectrometry （CF-IRMS） interfaced with a Gasbench Ⅱ was presented to determine chlorine stable isotope composition. Silver chloride （AgCl） was quantitatively derived from chloride by using silver nitrate （AgNO3）, and then was reacted with iodomethane （CH3Ⅰ） to produce methyl chloride （CH3Cl）. A GasBench Ⅱ equipped with a PoraPlot Q column was used to separate CH3Cl from any other gas species. Finally, chlorine stable isotope analysis was carried out on CH3Cl introduced to the IRMS in a helium stream via an active open split. The minimum amount of Cl used in this method is of the order of 1.4 μmol. Inter-laboratory and inter-technique comparisons show that the total uncertainty incorporating both the precision and accuracy of this method is better than 0.007%. Furthermore, ten seawaters sampled from different locations have a narrow δ37Cl value range from -0.008% to 0.010%, with a mean value of （0.000±0.006）%. This supports the assumption that any seawater can be representative of standard mean ocean chloride （SMOC） and used as an international reference material.

Seasonal changes in TC and WSOC and their ^13C isotope ratios in Northeast Asian aerosols： land surface–biosphere–atmosphere interactions

In order to understand the relative importance of anthropogenic and biological sources of carbonaceous aerosols in Northeast Asia,we measured total carbon(TC)and water-soluble organic carbon(WSOC)and their stable carbon isotope ratios(d^(13)C)in total suspended particulates collected from Sapporo,northern Japan(43.07°N,141.36°E)over a 1-year period(during 2 September 2009and 5 October 2010).Temporal variations of TC showed a gradual decrease from mid-autumn to winter followed by a gradual increase to growing season with a peak in early summer.Both d^(13)C_(TC)and d^(13)C_(WSOC)showed very similar temporal trends with a gradual enrichment of^(13)C from mid-autumn to winter followed by a depletion in the^(13)C to early summer and thereafter it remained stable,except for few cases.Based on the results obtained together with the air mass trajectories,we found that biogenic emissions including biological particles(e.g.,pollen)and secondary organic aerosol formation from biogenic volatile organic compounds are the important sources of carbonaceous aerosols in spring/summer whereas fungal spores from soil and biomass burning and enhanced fossil fuel combustion contribute significantly in autumn/winter and in winter,respectively,in Northeast Asia.

Late Paleozoic Mantle Source Nature of Tianshan Orogen, Northwest China: Evidence from the Geochemistry, Zircon U-Pb Dating, Hf and Whole Rock Sr-Nd-Pb Isotopes of the Mafic Dykes

The Tianshan Orogen(TO)is one of the largest typical accretionary orogenic belts in the world.Of which,the late Paleozoic was a critical era to understand the tectonic and geodynamic transition from accretion to collision.However,the late Paleozoic tectonic evolutionary history,especially for the time of the ocean-continent transition,is still debated although the origin and tectonic settings for the Paleozoic volcanic,felsic igneous magmatism in TO and reginal geology have been done in the last decades.In contrast,the researches on the mafic dykes in TO was not systematically carried out till now.Reginal-scale mafic dykes are commonly regarded as the products created in a extensional setting,and used to identify the major tectonic events such as rifting and continental break-up and further trace the mantle natures and geodynamic mechanism(Halls,1982;Bleeker and Ernst,2006;Li et al.,2008;Ernst et al.,2010;Srivastava,2011;Hou,2012;Peng,2015;Peng et al.,2019).There are widespread late Paleozoic mafic dykes beside the huge of intermediate-acid igneous rocks in the TO,being an idea object to reveal the extensional events,tectonic evolution and the mantle nature and geodynamic processes.We present the ICPMS in situ zircon U–Pb dating,Lu-Hf and whole-rock Sr-Nd isotopes as well as the geochemistry data for these mafic dykes to better constraint their petrogenesis and mantle nature.New zircon U-Pb dating for 12 samples from the representative basic dykes and basalts yield three distinct stages of^332 Ma,316–302 Ma and 288–282 Ma,respectively.In which,the first stage of mafic dykes is mainly occurred in both East Tianshan Orogen(ETO)and West Tianshan Orogen(WTO),and composed of dolerite with minor basalts.The second stage of mafic dyke also can be found in both ETO and WTO.However,in contrast to the first stage of mafic dykes,they have relatively variable rock types from the dolerite/or gabbros to gabbroic diorite.The third stage of mafic dykes are slightly intermediate in composition,and chiefly consist of andesitic-basaltic dolerite with some diorites.They are widely developed not only in both ETO and WTO,but also in the Beishan area to the east of the ETO,indicating a large-scale mafic magmatism in Tianshan and adjacent areas.

Evaluation on nitrogen isotopes analysis in high-C/N-ratio plants using elemental analyzer/isotope ratio mass spectrometry

Elemental analyzer/isotope ratio mass spectrometry(EA/TRMS) has been widely applied to analyze the^(15)N/^(14)N isotope composition(δ^(15)N) of plants and soils,but the δ^(15)N results may be inaccurate due to incomplete combustion of the high-C/N-ratio plant samples by EA.Therefore,it is necessary to develop a method to solve the problem of imperfect combustion.In this study,we used two methods:1) adding copper oxide powder to the samples,and 2) increasing the O_2 flow(from 100 mL min^(-1) to 200 mL min^(-1)) for the auto sampler inlet purge line of the EA.The δ^(15)N values of the plant samples became more positive and tended to be stable after complete combustion.Also,the required blank samples for each plant sample decreased with increasing amount of the added CuO powder.However,at 200 mL min^(-1) of the oxygen flow in the EA,complete combustion could not be achieved without adding copper oxide,but this was done with decreased amount of CuO powder.Therefore,mixing cupric oxide into the high-C/N-ratio samples was an efficient,simple and convenient way to solve the problem of imperfect combustion in the EA.

Carbon isotopic fractionation during vaporization of low molecular weight hydrocarbons(C6–C12)

Three series of laboratory vaporization experiments were conducted to investigate the carbon isotope fractionation of low molecular weight hydrocarbons（LMWHs）during their progressive vaporization.In addition to the analysis of a synthetic oil mixture,individual compounds were also studied either as pure single phases or mixed with soil.This allowed influences of mixing effects and diffusion though soil on the fractionation to be elucidated.The LMWHs volatilized in two broad behavior patterns that depended on their molecular weight and boiling point.Vaporization significantly enriched the ^13C present in the remaining components of the C6–C9 fraction,indicating that the vaporization is mainly kinetically controlled;the observed variations could be described with a Rayleigh fractionation model.In contrast,the heavier compounds（n-C10–n-C12）showed less mass loss and almost no significant isotopic fractionation during vaporization,indicating that the isotope characteristics remained sufficiently constant for these hydrocarbons to be used to identify the source of an oil sample,e.g.,the specific oil field or the origin of a spill.Furthermore,comparative studies suggested that matrix effects should be considered when the carbon isotope ratios of hydrocarbons are applied in the field.