中国区域气溶胶对东亚夏季风的可能影响(Ⅱ)：黑碳气溶胶及其与硫酸盐气溶胶的综合影响   总被引：8，自引：0，他引：8  

孙家仁  刘煜 《气候变化研究进展》2008,4(3):161-166

 利用NCAR的新一代GCM CAM3.0模式耦合一个气溶胶同化系统,研究了中国区域黑碳气溶胶的直接气候效应。结果显示,中国区域黑碳气溶胶引起全球平均辐射强迫为0.13 W/m2,导致除了青藏高原和广西以外的中国大部分地区降温,其中东北、四川和内蒙古中北部降温最显著。由此造成海陆温差缩小,气压差降低,从而总体上使东亚夏季风减弱。但与硫酸盐气溶胶的影响相比,黑碳气溶胶使季风减弱的程度较小,长江中下游地区的降水有所增加。黑碳气溶胶加强了中国东南部地区的对流活动,这与硫酸盐气溶胶的作用相反。同时,探讨了中国区域硫酸盐和黑碳气溶胶的综合直接气候效应。结果表明,硫酸盐和黑碳气溶胶的综合作用与仅有硫酸盐气溶胶的情形十分相似,降水变化的区域也和硫酸盐的保持一致。  相似文献   

Multiple sulfur isotope chemostratigraphy across the Permian–Triassic boundary at Chaotian,China: Implications for a shoaling model of toxic deep-waters     

Masafumi Saitoh  Yuichiro Ueno  Yukio Isozaki  Naohiro Yoshida 《Island Arc》2021,30(1):e12398

Previous studies on multiple sulfur isotopes (³²S, ³³S, and ³⁴S) in sedimentary pyrite at the end-Permian suggested a shoaling of anoxic/sulfidic deep-water contributing to the extinction. This scenario is based on an assumption that the sedimentary sulfur cycle was largely controlled by benthos activity, though a stratigraphic correlation between the sulfur records and ichnofabrics of the sediments at the end-Permian has not yet been examined. We report the multiple sulfur isotopic composition of pyrite in the Permian–Triassic boundary interval at Chaotian, South China. Our data can be generally explained by a mixing of sulfur in sulfide from two different sources: one produced via sulfate reduction in an open system with respect to sulfate and the other produced in a closed system. In particular, the former with the substantially low δ³⁴S (<−40 ‰) and high ∆³³S (up to +0.100 ‰) values was likely produced via water-mass sulfate reduction or via sulfate reduction in oxic sediments with common burrows. The frequent occurrence of small pyrite framboids (mostly <5 μm in diameter) in the Lopingian (Late Permian) Dalong Formation of deep-water facies supports the enhanced water-mass sulfate reduction in an anoxic deep-water mass. The negative ∆³³S values are observed only in the oxic limestones, and no substantial ∆³³S change is observed across the extinction horizon despite of the disappearance of bioturbation. Our results are apparently inconsistent with the previous shoaling model. We expand the model and infer that, when the deep-water was sulfidic and its shoaling rate was high, a substantial amount of hydrogen sulfide (H₂S) was supplied onto the shelf via the shoaling; that resulted in the positive ∆³³S value of the bulk sediments. The observed ∆³³S variation on a global scale suggests a substantial variation in H₂S concentration and/or in upwelling rate of shoaling deep-waters during the Permian–Triassic transition.  相似文献   

钾含量对白云母X射线衍射特征的影响   总被引：5，自引：1，他引：4  

王德强  王辅亚  王冠鑫  张惠芬 《大地构造与成矿学》2004,28(1):69-73

对白云母X射线衍射峰强度的理论计算,发现其衍射峰的强度随钾含量呈规律性变化;对白云母活化释钾后不同钾含量样品进行X射线衍射实验,发现实测的衍射峰强度值与计算值变化趋势一致。计算与实测的白云母特征衍射峰强度比值曲线也有相同的变化趋势。这些结果表明白云母中钾含量是其X射线衍射特征变化的主要原因。  相似文献   

云贵高原斜坡地带典型地下水富硫酸盐地区“越层找水”模式及其机理研究          下载免费PDF全文

曹建文  夏日元  方尚武  赵良杰  王喆  王若凡  易瑞 《中国地质》2019,46(2):235-243

地下水是中国西南云贵高原斜坡地带重要的饮用水源,其中黔中镇宁县北部存在大面积地下水中硫酸盐超标地区,导致了当地出现水质性缺水问题。本次研究通过岩相古地理分析、水化学分析、D、18O、34S同位素测试、岩样测试、岩心观察等技术手段,查明了研究区内地下水的补给源主要为大气降水,地下水中硫酸盐(SO_4~(2-))浓度在30～1100 mg/L,平均值为221.78 mg/L,呈现高度富集SO_4~(2-)的特点;在区域相对隔水层以上,不同类型地下水中SO_4~(2-)浓度大体具有机井上升泉下降泉溶潭地下河出口基岩裂隙泉表层岩溶泉的规律;探讨了地表水、地下水中SO_4~(2-)的来源,表层岩溶泉中硫酸根的来源主要为大气降水,高硫酸盐样品中硫酸根的来源主要为石膏溶解。在此基础上,结合钻井资料,掌握了研究区膏岩层分布及含水层结构特征,通过建立"越层找水"模式,采取下层低硫酸盐含水层,获取合格饮用水源,可有效解决当地水质性缺水问题。  相似文献   

伊犁蒙其古尔铀矿床含矿层砂岩中黄铁矿形成机制及对铀成矿的指示意义     

丁波  刘红旭  张宾  李平  蒋宏  张虎军  谢希良  郭春杰 《矿床地质》2019,38(6):1379-1391

蒙其古尔铀矿床为伊犁盆地南缘大型层间氧化带砂岩型铀矿床,为查明该矿床含矿层中黄铁矿成因及其形成机制,探讨微生物参与铀成矿过程。文章对含矿层砂岩中黄铁矿与铀矿物矿物学特征、黄铁矿S同位素与碳酸盐胶结物的C-O同位素开展细致研究。研究表明:①蒙其古尔铀矿床中铀主要以铀矿物与吸附铀形式存在,吸附铀主要为有机质吸附铀,铀矿物以沥青铀矿为主,多与黄铁矿、炭屑共生;②蒙其古尔铀矿床含矿层砂岩中黄铁矿主要以自形晶、草莓状和不规则状集合体产出,多与沥青铀矿、碳酸盐胶结物共生,其中黄铁矿S同位素(δ~(34)S_(V-CDT)=-68.4‰～22.1‰)与碳酸盐胶结物的C-O同位素(δ~(13)C_(V-PDB)=-10.2‰～-7.4‰,δ~(18)O_(V-PDB)=-9.6‰～-5.8‰)分析表明黄铁矿具有细菌硫酸盐还原(BSR)与有机物热解2种成因,并探讨了这2种不同成因黄铁矿的形成机制。③结合前人研究成果,认为硫酸盐还原菌(SRB)参与蒙其古尔铀矿床铀成矿过程,以间接还原方式为主,在有机质、黏土矿物与颗粒表面吸附U(Ⅵ)的基础上,通过硫酸盐还原菌(SRB)还原SO_4~(2-)产生的H_2S将U(Ⅵ)被还原成U(Ⅳ),形成铀矿物。  相似文献   

Chloride source delineation in an urban-agricultural watershed: Deicing agents versus agricultural contributions     

Andrew Oberhelman  Eric W. Peterson 《水文研究》2020,34(20):4017-4029

Analyses (n = 525) of chloride (Cl⁻), bromide (Br⁻), nitrate as nitrogen (NO₃-N), sodium (Na⁺), calcium (Ca²⁺) and potassium (K⁺) in stream water, tile-drain water and groundwater were conducted in an urban-agricultural watershed (10% urban/impervious, 87% agriculture) to explore potential differences in the signature of Cl⁻ originating from an urban source as compared with an agricultural source. Only during winter recharge events did measured Cl⁻ concentrations exceed the 230 mg/L chronic threshold. At base flow, nearly all surface water and tile water samples had Cl⁻ concentrations above the calculated background threshold of 18 mg/L. Mann–Whitney U tests revealed ratios of Cl⁻ to Br⁻ (p = .045), to NO₃-N (p < .0001), to Ca²⁺ (p < .0001), and to Na⁺ (p < .0001) to be significantly different between urban and agricultural waters. While Cl⁻ ratios indicate that road salt was the dominant source of Cl⁻ in the watershed, potassium chloride fertilizer contributed as an important secondary source. Deicing in watersheds where urban land use is minimal had a profound impact on Cl⁻ dynamics; however, agricultural practices contributed Cl⁻ year-round, elevating stream base flow Cl⁻ concentrations above the background level.  相似文献   

Geochemistry of Flooded Underground Mine Workings Influenced by Bacterial Sulfate Reduction     

Amber J. Roesler  Christopher H. Gammons  Gregory K. Druschel  Harry Oduro  Simon R. Poulson 《Aquatic Geochemistry》2007,13(3):211-235

Unlike the majority of the water in the flooded mine complex of Butte Montana, which includes the highly acidic Berkeley pit lake, groundwater in the flooded West Camp underground mine workings has a circum-neutral pH and contains at least 8 μM aqueous sulfide. This article examines the geochemistry and stable isotope composition of this unusual H₂S-rich mine water, and also discusses problems related to the colorimetric analysis of sulfide in waters that contain FeS_(aq) cluster compounds. The West Camp mine pool is maintained at a constant elevation by continuous pumping, with discharge water that contains elevated Mn (90 μM), Fe (16 μM), and As (1.3 μM) but otherwise low metal concentrations. Dissolved inorganic carbon in the mine water is in chemical and isotopic equilibrium with rhodochrosite in the mineralized veins. The mine water is under-saturated with mackinawite and amorphous FeS, but is supersaturated with Cu- and Zn-sulfides. However, voltammetry studies show that much of the dissolved sulfide and ferrous iron are present as FeS_(aq) cluster molecules: as a result, the free concentration of the West Camp water is poorly constrained. Concentrations of dissolved sulfide determined by colorimetry were lower than gravimetric assays obtained by AgNO₃ addition, implying that the FeS_(aq) clusters are not completely extracted by the Methylene Blue reagent. In contrast, the clusters are quantitatively extracted as Ag₂S after addition of AgNO₃. Isotopic analysis of co-existing aqueous sulfide and sulfate confirms that the sulfide was produced by sulfate-reducing bacteria (SRB). The H₂S-rich mine water is not confined to the immediate vicinity of the extraction well, but is also present in flooded mine shafts up to 3 km away, and in samples bailed from mine shafts at depths up to 300 m below static water level. This illustrates that SRB are well established throughout the southwestern portion of the extensive (>15 km³) Butte flooded mine complex.  相似文献   

作物生长岩-土环境中不同存在形态钾素含量动态变化   总被引：1，自引：0，他引：1  

朱立新  马生明 《物探与化探》1999,23(2):97-103

以较系统的观测资料,对土壤环境中的缓效态、速效态、水溶态钾素含量的动态变化进行探索.结果表明,缓效态钾的季节性动态变化制约着速效态、水溶态钾的季节性动态变化,但是后两者变化幅度较缓效态钾的大;这种动态变化同时受土壤类型和深度的影响.  相似文献   

陆相咸化湖泊沉积硫酸盐岩硫同位素组成及其地质意义   总被引：1，自引：0，他引：1  

彭立才  杨平  濮人龙 《矿物岩石地球化学通报》1999,(2)

现代海洋中的硫酸盐矿物和海水硫酸盐本身常有相似的硫同位素组成,因而可根据现代蒸发岩的硫酸盐同位素来判断古环境。据李任伟［１］引用Ｈｏｌｓｅｒ和Ｋａｐｌａｎ及格里年科的资料报道,海相蒸发岩及其所反映的古海洋硫酸盐的硫同位素组成只在较狭窄的范围内变化,现...  相似文献   

Metamorphic charnockite in contact aureoles around intrusive enderbite from Natal, South Africa     

Alfons M. van den Kerkhof  Geoffrey H. Grantham 《Contributions to Mineralogy and Petrology》1999,137(1-2):115-132

In the Port Edward area of southern Kwa-Zulu Natal, South Africa, charnockitic aureoles up to 10 m in width in the normally garnetiferous Nicholson's Point Granite, are developed adjacent to intrusive contacts with the Port Edward Enderbite and anhydrous pegmatitic veins. Mineralogical differences between the country rock and charnockitic aureole suggest that the dehydration reaction Bt + Qtz → Opx + Kfs + H₂O and the reaction of Grt + Qtz → Opx + Pl were responsible for the charnockitization. The compositions of fluid inclusions show systematic variation with: (1) the Port Edward Enderbite being dominated by CO₂ and N₂ fluid inclusions; (2) the non-charnockitized granite by saline aqueous inclusions with 18–23 EqWt% NaCl; (3) the charnockitic aureoles by low-salinity and pure water inclusions (<7 EqWt% NaCl); (4) the pegmatites by aqueous inclusions of various salinity with minor CO₂. As a result of the thermal event the homogenization temperatures of the inclusions in charnockite show a much larger range (up to 390 °C) compared to the fluid inclusions in granite (mostly <250 °C). Contrary to fluid-controlled charnockitization (brines, CO₂) which may have taken place along shear zones away from the intrusive body, the present “proximal” charnockitized granite formed directly at the contact with enderbite. The inclusions indicate contact metamorphism induced by the intrusion of “dry” enderbitic magma into “wet” granite resulting in local dehydration. This was confirmed by cathodoluminescence microscopy showing textures indicative for the local reduction of structural water in the charnockite quartz. Two-pyroxene thermometry on the Port Edward Enderbite suggests intrusion at temperatures of ∼1000–1050 °C into country rock with temperature of <700 °C. The temperature of aureole formation must have been between ∼700 °C (breakdown of pyrite to form pyrrhotite) and ∼1000 °C. Charnockitization was probably controlled largely by heat related to anhydrous intrusions causing dehydration reactions and resulting in the release and subsequent trapping of dehydration fluids. The salinity of the metamorphic fluid in the contact zones is supposed to have been higher at an early stage of contact metamorphism, but it has lost its salt content by K-metasomatic reactions and/or the preferential migration of the saline fluids out of the contact zones towards the enderbite. The low water activity inhibited the localized melting of the granite. Mineral thermobarometry suggests that after charnockite aureole genesis, an isobaric cooling path was followed during which reequilibration of most of the aqueous inclusions occurred. Received: 8 November 1998 / Accepted: 21 June 1999  相似文献