全边界层选用相似理论对O3、NOx浓度及沉降的影响

将广泛应用于东亚地区的LLA(Lurmann Lloyd Atkinson)化学机制耦合到欧拉型区域空气质量模式(RAQM),并考虑区域污染物长期模拟研究中降水随时间变化的非均匀性,讨论了湍流参数化过程中相似理论在近地层和全边界层的应用对湍流垂直扩散系数(Kz)与干沉降速度(V),O3与NOx浓度的影响。结果表明,全边界层应用相似理论明显低估了Kz值,近地层50m处Kz值被低估20%以上,750m处其值被低估约70%;O3、NOx的干沉降速度在日本东部与南部海域被低估了10%以上,在朝鲜半岛东部和西部海域模拟值普遍偏高。Kz和干沉降速度的不同直接影响污染物的浓度和沉降量分布。Kz值的被低估对NOx浓度有明显影响,在近地层50m处NOx浓度最大可增加约30%,整个边界层中NOx平均浓度除台湾省东北海域外普遍增加5%~20%。O3浓度则受干沉降作用的影响较大。虽然近地层、全边界层分别应用相似理论都较好地模拟了O3与NOx峰值浓度出现的时间,但相似理论应用于全边界层会引起较大的误差。即使是大区域、长期空气质量模拟研究,也建议相似理论仅应用于近地层,且模式第一层高度应设置在常通量层内。     

华东稻麦轮作农田CH4、N2O和NO排放特征

利用同步自动观测系统对华东稻麦轮作农田的CH4、N2O和NO排放进行了长期连续观测,分析了这3种气体排放的季节特征及决定因素,结果表明,华东稻麦轮作农田的CH4、N2O和NO排放具有完全不同的季节变化形式。CH4的排放发生在水稻生长期,其他阶段排放不明显,土壤水分状况是决定整个轮作周期内CH4排放变化的主要因素。N2O排放具有"冬季无,水田少,旱地多"的季节变化特点,尤其以旱地阶段的排放为主,土壤水分状况和温度共同决定着N2O排放的季节变化形式。NO排放具有"冬季无,水田很少,春季旱地多于秋季旱地"的季节分布特点,轮作周期内97.3%±0.6%的NO排放都发生在除冬季以外的旱地阶段,NO排放的季节变化形式由土壤水分状况和温度共同决定。大多数情况下稻田CH4和N2O排放呈互为消长的关系,但在烤田期间,二者却有时甚至同时出现高排放。在N2O日平均排放通量小于5 mg.m-2.h-1时,稻麦轮作农田的N2O和NO排放呈明显的互为消长关系,但大于5 mg.m-2.h-1时,N2O排放很强,同时NO排放也很强。     

Acceleration of a spherical neutral shell produced by an ionization-shock front in an inhomogeneous interstellar medium

We numerically model the formation and acceleration of a neutral gas shell as an ionization-shock front propagates in a spherical cloud by taking into account the photoionization and radiative heating of the gas, the spectral radiative transfer. We suggest and implement an approximation of the cooling function that allows calculations to be performed in a wide range of gas ionization fractions and temperatures. The total mass, average velocity, and thickness of the shell have been determined. The results are compared with approximate formulas known in the literature. Based on the parameters of the shell found, we estimate its acceleration, characteristic scales, and the growth times of unstable perturbations. We analyze the influence of the cloud particle density, cloud radius, stellar temperature, and radiation spectrum on the integrated characteristics of the neutral gas in the layer between the ionization and shock fronts. The distribution of matter in the shell and its thickness are shown to differ significantly from those used in approximate models.     

Evaluation of oxygen isotopes in carbonate as an indicator of lake evolution in arid areas: The modern Qinghai Lake, Qinghai–Tibet Plateau

The oxygen isotopic composition of carbonate in lakes has been used as a useful indicator in Palaeolimnological research, and has made some important contributions to our understanding of lacustrine systems. For modern lakes in arid or cold areas, however, there are few data available to test the effect of lake salinity and temperature on the oxygen isotopic composition of various carbonate sources such as ostracod, bulk carbonate, and fine-grained carbonate (< 60 μm). Here we examined the oxygen isotopic composition of ostracods, bulk carbonate, and fine-grained carbonates, as well as that of coexisting water from Lake Qinghai and the smaller surrounding lakes and ponds on the Qinghai–Tibet Plateau. Our investigation highlights three key effects. First, the oxygen isotopic composition of ostracods, bulk carbonate, and fine-grained carbonate in the lakes and ponds shows a clear response to lake water δ¹⁸O values, and these vary with water salinity. The relationship between lake water δ¹⁸O and salinity is not only dominated by the evaporation/freshwater input ratios, but is also controlled by the distance to the mouth of the major rivers supplying to the lake. Second, the ostracod, bulk carbonate, and fine-grained carbonate show similar isotopic change trends in the study area, and oxygen isotopic differences between ostracods and authigenic carbonate may be explained by the different water temperatures and very small ‘vital offsets’ of ostracods. Finally, the effect of water depth on temperature leads to increasing δ¹⁸O values in carbonates as water depth increases, both in benthic ostracods living on the lake bottom, as well as in bulk carbonate precipitated at the water surface.For arid, high-altitude Lake Qinghai, our results suggest that variations in the δ¹⁸O values of carbonate in Lake Qinghai are mainly controlled by the oxygen-isotope ratio of the lake water changing with water salinity. As a secondary effect, increasing water depth leads to cooler bottom and surface water, which may result in more positive δ¹⁸O values of ostracod and bulk carbonate.     

Pb-Pb dating of black shales from the Lower Cambrian and Neoproterozoic strata, South China

Black shales occur widely in the Lower Cambrian and Neoproterozoic strata on the Yangtze Platform, South China. In this study, Lower Cambrian black shales from Xiuning section and Late Neoproterozoic black shales from Weng’an section were studied and Pb isotopic compositions were analyzed following a stepwise acid-leaching technique. The ²⁰⁶Pb/²⁰⁴Pb ratios in both sections show large variations, from 18.906 to 43.737 in the Weng’an section and from 24.811 to 38.110 in the Xiuning section. In contrast, the ranges for ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb values in both sections are relatively smaller from 15.649 to 17.126 and 37.744-38.199 in the Weng’an section, and from 16.034 to 16.783 and 38.602-39.391 in the Xiuning section, respectively. These data yielded two Pb isotope isochron ages of 536±39 and 572±36 Ma, respectively. These ages well accord with other published data and we suggest that they represent the depositional ages for the Lower Cambrian Hetang Formation and the upper Neoproterozoic Doushantuo Formation in South China.     

Decompression and H<Subscript>2</Subscript>O exsolution driven crystallization and fractionation: development of a new model for low-pressure fractional crystallization in calc-alkaline magmatic systems

Magma ascent, decompression-induced H₂O exsolution and crystallization is now recognized as an important process in hydrous subduction zone magmas. During the course of such a process calculations suggest that the ascent rate of a degassing and crystallizing mafic magma will be greater than crystal settling velocities. Thus, any crystals formed as a consequence of volatile exsolution will remain suspended in the magma. If the magma erupts before the percentage of suspended crystals reaches the critical crystallinity value for mafic magma (~55 vol.%) it will produce the commonly observed crystal rich island arc basalt lava. If the magma reaches its critical crystallinity before it erupts then it will stall within the crust. Extension of compaction experiments on a 55 vol.% sand-Karo syrup suspension at different temperatures (and liquid viscosities) to the likely viscosities of interstitial andesitic to dacitic liquid within such a stalled magma suggest that small amounts (up to ~10%) can be expelled on a time scale of 1–10 years. The expelled liquid can create a new intermediate to silicic body of magma that is related to the original mafic magma via fractional crystallization. The short time scale for liquid expulsion indicate that decompression-induced H₂O exsolution and crystallization can be an important mechanism for fractional crystallization. Based on this assumption a general model of decompression-induced crystallization and fractionation is proposed that explains many of the compositional, mineralogical and textural features of Aleutian (and other andesites).     

中国东部陆下岩石圈地幔中的再循环地壳流体组分

地幔捕虏体中的流体组分记录了地幔演化的信息,可用来认识地幔中再循环地壳组分的性质和来源。采用分步加热质谱法测定中国东部二辉橄榄岩捕虏体组成矿物中流体挥发份的碳、氢和氧同位素组成,结合化学组成(Zhang et al., 2004)综合分析表明,早期流体包裹体、矿物晶格缺陷和空隙中的流体挥发分主要在高温段(800-1200°C)释出,CO2和CO显示较轻的δ13C值,与世界其它地区地幔捕虏体明显不同;晚期流体包裹体中的流体挥发分主要在低温段(300-600°C)释出。根据中国东部地幔演化事件、地幔矿物性质认为陆下岩石圈地幔中三种类型的流体挥发份中均存在来源不同的再循环地壳组分：（1）地幔初始流体：主要为耐熔矿物橄榄石在800-1200°C释出的流体组分,华北克拉通地幔初始流体的化学组成（主要为CO）与华南克拉通（主要为CO2）明显不同,反映二者拼合前各自演化时期捕获的流体组分。地幔特征的δD、δ13CCH4和δ18OCO2反映初始流体组分可能为元古代克拉通大陆型岩石圈地幔成分,较轻的CO2 和 CO的δ13C值揭示初始流体中存在部分再循环地壳流体,可能在1.9Ga的大陆碰撞过程中混入。（2）地幔交代流体：指斜方辉石和单斜辉石800-1200°C释气峰的流体组分,以H2为主。华北克拉通交代流体主要组分H2含量(80.73 mm3.STP/g) 明显低于华南克拉通(138.91 mm3.STP/g),地幔特征的δDH2和δ13CCH4表明交代流体主体为地幔来源,较轻的δ13CCO2,CO和较重δ18OCO2揭示其中存在再循环陆壳流体,其可能的来源为华北与华南中生代拼合过程中的壳幔相互作用。（3）岩石圈减薄流体：指二辉橄榄岩捕虏体组成矿物在400-600°C释放出的流体,华北与华南克拉通在流体组成方面相似,壳源特征的CO2、CO和CH4的δ13C值,以及较轻的δ18OCO2和δDH2O值指示该流体可能为岩石圈地幔减薄过程中引起的再循环洋壳流体,可能与中国东部转换带中水平俯冲的太平洋岩石圈(或其前身)脱气有关。     

Combined Sr isotope and trace element analysis of melt inclusions at sub-ng levels using micro-milling, TIMS and ICPMS

This paper describes a technique, which allows precise and accurate Sr isotope measurement combined with trace element analysis of individual melt inclusions, of sample sizes  1 ng of Sr. The technique involves sampling by micro-milling, chemical dissolution, micro Sr column chemistry, TIMS, and ICPMS analyses. A 10% aliquot of each sample solution is used for trace element analysis by double focusing magnetic sector field ICPMS, while Sr is chemically separated from the remaining 90% and used for ⁸⁷Sr/⁸⁶Sr determinations by TIMS.During the development of the technique outlined above, we documented in detail the potential sources of blank contributions and their magnitude. The average size and Sr isotope composition of our laboratory total procedural blank during this study was 5.4 pg ± 0.3 pg Sr (n = 21) with an ⁸⁷Sr/⁸⁶Sr of 0.7111 ± 0.0002 (2SE, n = 3). The total procedural Rb blank was 1.9 ± 0.7 pg (n = 21). The total procedural blank was found to have minimal effect (< 150 ppm shift) on the ⁸⁷Sr/⁸⁶Sr of sample material containing down to  250 pg Sr. Applying a blank correction allows ‘in house’ standards of this size to be corrected back to within 175 ppm of their accepted values. By applying blank corrections we can confidently measure the Sr isotope composition on sample sizes down to  25 pg Sr to an accuracy better than 400 ppm.The utility of the technique is illustrated by application to a suite of melt inclusions from NW Iceland and their host olivines. It is shown that the effect of a small amount of entrainment of the host olivine during sampling of 50 μm melt inclusions has a negligible effect on the measured Sr isotope and trace element composition. Furthermore, where melt inclusions are < 50 μm it is possible to obtain Sr isotope and trace element data on multiple melt inclusions hosted in a single olivine. This provides similar information to that of the single melt inclusions.     

Light hydrocarbons geochemistry of surface sediment from petroliferous region of the Mehsana block,North Cambay Basin

A study was carried out to test the usefulness of surface geochemical methods as regional evaluation tools in petroliferous region of the Mehsana block, North Cambay Basin. A suite of 135 soil samples collected from the depth of 2.5 m, were analyzed for adsorbed light gaseous hydrocarbons and carbon isotopes (δ¹³C_methane and δ¹³C_ethane). The light gaseous hydrocarbon analysis show that the concentration ranges 402 ppb, 135 ppb, 70 ppb, 9 ppb and 18 ppb of C₁, C₂, C₃, iC₄ and nC₄, respectively. The value of carbon isotopic ranges of methane −29.5 to −43.0‰ (PDB) and ethane −19.1 to −20.9‰ (PDB). This data, when mapped, indicates patterns coinciding with major known oil and/or gas field of Sobhasan/Linch in this study area. The existence of un-altered petroliferous microseeps of catagenetic origin is observed in the study area. A regional study, such as the one described here, can provide important exploration facts concerning the regional hydrocarbon potential in a block. This method has been confirmed and can be applied successfully in frontier basins.