云南白水台钙华水池中水化学日变化及其生物控制的发现   总被引：11，自引：0，他引：11  

刘再华  李强  孙海龙  汪进良  吴孔运 《水文地质工程地质》2005,32(6):10-15

为弄清云南白水台泉及其下游钙华水池中水化学的日变化,选取1号泉及其流经的两个钙华水池(6号和10号)作为研究对象并对其水温、pH值和电导率进行了自动监测。根据Ca2 、HCO3-与电导率存在的线性关系,用WATSPAC软件计算了水中方解石的饱和指数和PCO2。监测发现:泉水不存在显著的水化学日动态变化,而两个钙华水池表现出显著的日动态变化。其中10号钙华水池在白天温度较高时水中的CO2大量逸出并通过水下水生植物的光合作用加速了水中碳酸钙的沉积。6号钙华水池水生植物生长茂盛,其叶片和部分枝干露出水面,因而光合作用主要发生在空中,所以此处水化学表现为白天pH值降低和电导率升高的反常现象,即由温度主导的根呼吸作用,在白天释放更多的CO2进入水体而使沉积下来的碳酸钙重新溶解。  相似文献   

方解石脉双晶纹方法在工程勘察中的应用   总被引：1，自引：1，他引：1  

蒋建平  章杨松  罗国煜  储同庆  阎长虹 《岩土力学》2002,23(2):184-190

在工程区基岩被第四纪土、江水等覆盖的情况下，如何充分利用好获得的钻孔岩芯来分析断层的发育和活动性情况就显得非常重要。为此，地基勘察中引入一种显微构造分析方法，即方解石脉双晶纹分析方法。方解石脉双晶纹能解决断层的活动期次、每一期次的强度、断层应力场、断层性质、断层活动时的环境条件和最后一次活动的时代等问题。由于方解石脉双晶纹发育的广泛性，使之具有推广价值。  相似文献   

重质碳酸钙干法超细与改性一体化工艺研究          下载免费PDF全文

王林江  苏达谋等 《地质与勘探》2001,37(2):72-73

在气流粉碎机中对重质碳酸钙进行干法超细与改性一体化工艺研究，通过控制改性剂种类，改性剂用量，给料粒度，给料速度，产品活化率达97％，吸油率16．20％，20天吸水率7．01％，白度91．5，粒度（d50)8.0um，碳酸钙的吸水和吸油率的均降低，对超细与改性一体化机理进行了讨论。  相似文献   

白云鄂博碳酸岩墙碳氧同位素地球化学   总被引：7，自引：3，他引：7  

舒勇  郑永飞  魏春生  周建波  杨学明  杨晓勇 《地球化学》2001,30(2):169-176

对内蒙古白云鄂博 REE- Fe- Nb矿床周围碳酸岩墙中共存的方解石和白云石进行了 C和 O同位素分析。结果表明，方解石和白云石的δ 13C值变化范围一致，均为－ 3.5‰～－ 7.3‰，落在正常地幔δ 13C值范围 (－ 5‰± 2‰ )内；而它们的δ 18O值可分为两组，第Ⅰ 组为 9.5‰～ 18.0‰，第Ⅱ 组为 20.6‰～ 22.6‰，均远大于正常地幔δ 18O值范围 (5.7‰± 1.0‰ )。第Ⅰ 组低δ 18O值样品中共存白云石与方解石之间的 C和 O同位素分馏均为负值，因此处于热力学不平衡状态，指示它们自形成后受到过后期热液蚀变，与先前的岩石学观察一致。相反，第Ⅱ 组高δ 18O值样品中白云石与方解石之间的 C和 O同位素分馏均为正值，处于热力学平衡状态，指示它们自形成后未受到后期热液蚀变，因此可能沉淀于晚期低温高δ 18O值流体。第Ⅰ 组碳酸岩墙中白云石的 C和 O同位素组成不呈线性分布，指示碳酸岩浆并非由幔源碳酸盐与沉积碳酸盐混合形成。应用水-岩交换模型计算得到，第Ⅰ 组碳酸岩在侵位后经历了碳酸岩浆期后热液的不均一蚀变，蚀变温度约在 220～ 800℃之间，蚀变流体的 CO2/H2O比值较小 (1/500)，但水 /岩比值变化较大 (10～ 400)。由于低温下方解石与热液之间的碳氧同位素交换速率大于白云石，导致这部分碳酸  相似文献   

An Overview of Dissolved and Suspended Matter Fluxes in the Loire River Basin: Natural and Anthropogenic Inputs   总被引：7，自引：0，他引：7  

Cécile Grosbois  Philippe Négrel  Daniel Grimaud  Christian Fouillac 《Aquatic Geochemistry》2001,7(2):81-105

The spatial and temporal distributions of major elements were investigated in the surface waters and in associated suspended matter at two sites of the upper Loire basin (Orleans and Brehemont) between 1995 and 1998.According to geochemical and isotopic patterns, the dissolved load appears to result from a process of mixing rainwater inputs, weathering processes of carbonate and silicate bedrock, and agricultural and urban inputs. Natural inputs influence 60% of water chemical composition at both sites. Annual dissolved fluxes were estimated to be 1300 10³ t/y at Orleans and 1620 10³ t/y at Brehemont. Major elements are transported mainly in the dissolved fraction. After correcting for atmospheric and anthropogenic inputs, the silicate specific export rate was calculated to be 11 t/y/km² throughout the basin and the carbonate specific export rate to be from 47 t/y/km² at Orleans to 23 t/y/km² at Brehemont.The suspended load appears to result from at least two particle reservoirs: a silicate reservoir and a carbonate reservoir. The silicate reservoir has a detrital origin, mainly during periods of high flow, while the carbonate reservoir has a detrital origin during periods of high flow and an authigenic origin during periods of low flow. Of the total annual flow of suspended matter, this authigenic material represents 16% at Orleans, 25% at Brehemont and 37% in the fluvial part of the estuary. After correcting authigenic inputs, the specific export rate due to mechanical weathering was estimated to be 8 t/y/km² throughout the Loire basin.  相似文献   

Oxygen and Carbon Isotope Study of Calcite and Dolomite in the Disseminated Au-Ag Telluride Bulawan Deposit, Negros Island, Philippines     

Victor B. MAGLAMBAYAN  Daizo ISHIYAMA  Toshio MIZUTA  Osamu MATSUBAYA  Yohei ISHIKAWA 《Resource Geology》2001,51(2):107-116

Abstract: The disseminated Au‐Ag telluride Bulawan deposit, Negros island, Philippines, is hosted by dacite porphyry breccia pipes which formed in a Middle Miocene dacite porphyry stock. Electrum and Au‐Ag tellurides occur mostly as grains intergrown with or filling voids between sphalerite, pyrite, chalcopyrite, galena and tennantite. Calcite, quartz and rare dolomite are the principal gangue minerals. Four types of alteration were recognized in the deposit, namely; propylitic, K‐feldspar‐sericitic, sericitic and carbonate alteration. Carbonate alteration is correlatable to the gold deposition stage and occurs mostly along fault zones. The δ¹⁸O and δ¹³C compositions of calcite and dolomite in propylite zone and ore‐stage dacite porphyry breccia were determined. The δ¹⁸O values of calcite in propylitized andesite range from +12.2 to +14.7%, and their δ¹³C values range from ‐6.1 to ‐1.0%. The δ¹⁸O values of calcite and dolomite in sericite‐ and carbonate‐altered, mineralized dacite porphyry breccia and dacite porphyry rocks range from +15.1 to +23.1%, and the δ¹³C values of calcite and dolomite range from ‐3.9 to +0.9%. The δ¹⁸O and δ¹³C values of the hydrothermal fluids were estimated from inferred temperatures of formation on the basis of fluid inclusion microthermometry. The δ¹⁸O values of hydrothermal fluid for the propylitic alteration were calculated to be +8.5 ‐ +9.5%, assuming 375°C. On the other hand, the δ¹⁸O values of ore solutions for base metal and Au mineralization were computed to be +13.6 ‐ +14.6%, assuming 270°C. The hydrothermal fluids that formed the Bulawan deposit are dilute and ¹⁸O‐enriched fluids which reacted with ¹⁸O‐ and ¹³C‐rich wallrocks such as limestone.  相似文献   

An 8.1Ma calcite record of Asian summer monsoon evolution on the Chinese central Loess Plateau   总被引：5，自引：0，他引：5  

Chen XiuLing  Fang XiaoMin  An ZhiSheng  Han WenXia  Wang Xin  Bai Yan  Hong Ye 《中国科学D辑(英文版)》2007,50(3):392-403

Carbonates in loess-red clay sequences consist mainly of calcite and dolomite. The EDTA analysis of carbonates in different size fractions and magnetic susceptibility reveal that calcite is a sensitive index of summer monsoon. The chemical analysis of carbonates and calcite from an 8.1 Ma loess-red clay sequence at Chaona on the Chinese central Loess Plateau shows that the evolution of the Asian summer monsoon experienced four stages, namely 8.1―5.5 Ma, 5.5―2.8 Ma, 2.8―1.5 Ma and 1.5―0 Ma, with increasing intensification and fluctuation, suggesting a possible combining impacts of uplift of the Tibetan Plateau and global changes on the Asian summer monsoon.  相似文献   

Flotation Separation of Trace Elements from Alkaline-Earth Matrices by Co(III) Hexamethylenedithiocarbamate before ICP-AES Determination     

Vesna Zajkova Paneva  Katarina Cundeva  Trajce Stafilov 《Geostandards and Geoanalytical Research》2007,31(1):51-60

A method for the selective separation of Ag, Cd, Cr, Cu, Ni, Pb and Zn in traces from solutions of calcite (CaCO₃), dolomite (CaMg(CO₃)₂) and gypsum (CaSO₄.2H₂O) before their determination by inductively coupled plasma-atomic emission spectrometry (ICP-AES) is presented. The expected interferences of Ca and Mg on intensities of trace analytes were removed by collecting the elements of interest with cobalt(III) hexamethylenedithiocar-bamate, Co(HMDTC)₃. The flotation of aqueous solutions (1 l) of calcite, dolomite and gypsum was performed at pH 6.0, by 1.5 mg l⁻¹ Co and 0.6 mmol l⁻¹ HMDTC⁻. To minimise the effect of the reaction between Ca/Mg, which restrains the function of the surfactant, careful selection of the most suitable foaming reagent was necessary. The accuracy of the method was established by analysing natural alkaline-earth minerals by the standard addition method as well as using the dolomite reference materials GBW 07114 and GSJ JDo-1. The ICP-AES limits of detection following flotation on different minerals were found to be 0.080 μg g⁻¹ for Cd, 0.105 μg g⁻¹ for Ag, 0.142 μg g⁻¹ for Cu, 0.195 μg g⁻¹ for Cr, 0.212 μg g⁻¹ for Ni, 0.235 μg g⁻¹ for Zn and 0.450 μg g⁻¹ for Pb.  相似文献   

清江高坝洲地区古岩溶角砾岩特征及形成条件   总被引：5，自引：0，他引：5  

王增银  沈继方 《地球科学》1998,23(5):524-528

古岩溶角砾岩是在特定的地质和水文地质条件下形成的沉积岩,是记录岩溶发育环境和形成时代的“化石”通过对高坝洲地区古岩溶角砾岩发育特征及取样分析测试研究,查明该类岩角砾岩属于岩溶崩塌角砾岩,胶结物方解石晶体是中低温热水溶液中ＣａＣＯ３沉淀形成的,形成时间是上新世。  相似文献   

不同阻垢剂对方解石和磷酸钙表面电位的影响   总被引：7，自引：0，他引：7  

王京  陆婉珍 《岩矿测试》1998,17(4):241-248

采用微电泳法考察了１５种阻垢剂对方解石和磷酸钙颗粒表面电位的影响。实验结果表明,在各种药剂中,丙烯酸／２丙烯酰胺基２甲基丙磺酸／次磷酸调聚物对难溶盐表面电位影响最大,乙二胺四乙酸二钠盐的影响最小。乙二胺四甲叉膦酸的溶垢能力和对表面电位的影响都较强。各种药剂对两种难溶盐表面电位影响的排序差异不显著。根据配位化学和表面化学原理解释了实验结果。  相似文献