红海及亚丁湾间之海水交换     

陈镇东  吴朝荣 《热带海洋学报》1993,(4)

分析表观耗氧量、滴定碱度及总二氧化碳量等资料来研判红海及亚丁湾间之海水交换。结果显示,红海深层水的方解石及霰石饱和度均比亚丁湾和阿拉伯海深层水的饱和度高。红海全水柱之方解石和霰石都处於过饱和状态,亚丁湾和阿拉伯海中各深度之方解石亦呈过饱和状态,但霰石的饱和探度则大约在500m左右。分析深层水之生物体无机碳与有机碳的分解比值,可以发现此地区深层水中,大约有25％的总二氧化碳增加量是由无机碳酸钙溶解而来。  相似文献   

Impact of Montmorillonite and Calcite on Release and Adsorption of Cyanobacterial Fatty Acids at Ambient Temperature   总被引：1，自引：0，他引：1  

刘邓  杨小芬  王红梅  李继红  苏念 《中国地质大学学报(英文版)》2008,19(5):526-533

Minerals might act as important sorbents of sedimentary organic matter and reduce biodegradation, which favors the formation of hydrocarbon source rocks in the earth's history. Since most organic matter is degraded during the sinking process, at ambient temperature, it is important to investigate the adsorption capacity of different minerals during this process, to assess the organic loss from primary productivity to sedimentary organic matter. In this study, montmorillonite and calcite have been selected to study the impact of different minerals on the release, adsorption, and deposition of cyanobacterial (Synechococcus elonpata) fatty acids (FAs) at ambient temperature. Gas chromatography (GC), gas chromatography-mass spectrometry (GC-MS) have been utilized to detect the variation in fatty acids. Primary results suggest that minerals have a different impact on dissolved organic matter. Montmorillonite can specifically enhance the release of fatty acids from cyanobacterial cells by lowering the pH values of the solution. The adsorption of the dissolved organic matter by montmorillonite will also be enhanced under a lower pH value. Conjunction of fatty acids with montmorillonite to form a complex will favor the sinking and preservation of these organics. Selective adsorption is observed among fatty acids with different carbon numbers. In contrast, calcite does not show any impact on the release and adsorption of organic matter even though it is reportedly capable of acting as a catalyst during the transformation of organic matter at high temperature. The primary data bridge a link between primary productivity and sedimentary organic matter, suggesting the relative importance of claystones in the formation of hydrocarbon source rocks in the earth's history.  相似文献   

利用矿物方解石进行水体除磷实验研究   总被引：4，自引：0，他引：4  

许虹  张静  高一鸣 《地学前缘》2008,15(4):138-141

为探索解决水体富营养化问题的新方法,利用矿物方解石对含磷溶液进行了除磷实验。实验结果表明,方解石晶芽可以促进磷的沉淀,降低溶液磷浓度;其降磷效果与溶液初始磷浓度有关,初始磷浓度为1.2mg/L,除磷率为12.68%,初始磷浓度为3mg/L,除磷率为69.94%,初始磷浓度为5mg/L,除磷率为88.48%;同样,实验温度升高,可使方解石降磷效果明显提高。经透射电子显微镜测试,除磷沉淀物没有明显的晶质体特征。  相似文献   

微生物对碳酸盐岩的风化作用   总被引：7，自引：0，他引：7  

连宾  陈烨  朱立军  杨瑞东 《地学前缘》2008,15(6):90

微生物-矿物相互作用可以促进许多表生生物地球化学反应过程,是表生地球化学研究的重要内容。通过综合岩石表面的微生物类群及其地质作用,分析碳酸盐岩微生物风化的各种现象,特别是微观尺度上的各种形态,阐述碳酸盐岩的微生物风化机制与风化产物,笔者提出微生物对碳酸盐岩风化的4种途径:(1)通过微生物在岩石表面和缝隙中生长,导致岩石表层发生生物溶蚀、生物磨蚀和生物钻孔作用,加速岩石风化进程;(2)微生物群体形成的钻孔网络可以增强岩石化学溶蚀的有效表面积并导致其表面强度减弱而促进机械侵蚀作用,微生物对周围岩石颗粒胶结结构的破坏、疏松作用也会导致岩石矿物颗粒的分解;(3)微生物的持水作用,微生物分泌的有机酸以及微生物呼吸所释放的CO2对岩表水分的酸化过程亦加速岩石矿物的分解;(4)微生物生长过程中从岩石内摄取营养元素和产生复杂的有机配体,能促进矿物元素的释放。文中提出在开展微生物对碳酸盐岩风化过程和机理研究的基础上,有必要引入微生物生物技术来综合开发本地低品位含钾磷矿产资源,加速岩溶地区山地土壤的形成与演化。  相似文献   

Paleohydrology and paleochemistry of Lake Manitoba,Canada: the isotope and ostracode records   总被引：1，自引：1，他引：0  

William M. Last  James T. Teller  Richard M. Forester 《Journal of Paleolimnology》1994,12(3):269-282

Lake Manitoba, the largest lake in the Prairie region of North America, contains a fine-grained sequence of late Pleistocene and Holocene sediment that documents a complex postglacial history. This record indicates that differential isostatic rebound and changing climate have interacted with varying drainage basin size and hydrologic budget to create significant variations in lake level and limnological conditions. During the initial depositional period in the basin, the Lake Agassiz phase (12–9 ka), ¹⁸O of ostracodes ranged from –16 to –5 (PDB), implying the lake was variously dominated by cold, dilute glacial meltwater and warm to cold, slightly saline water.Candona subtriangulata, which prefers cold, dilute water, dominates the most negative ¹⁸O intervals, when the basin was part of proglacial Lake Agassiz. At times during this early phase, the ¹⁸O of the lake abruptly shifted to higher values; euryhaline taxa such asC. rawsoni orLimnocythere ceriotuberosa, and halobiont taxa such asL. staplini orL. sappaensis are dominant in these intervals. This positive covariance of isotope and ostracode records implies that the lake level episodically fell, isolating the Lake Manitoba basin from the main glacial lake.¹⁸O values from inorganic endogenic Mg-calcite in the post-Agassiz phase of Lake Manitoba trend from –4 at 8 ka to –11 at 4.5 ka. We interpret that this trend indicates a gradually increasing influence of isotopically low (–20 SMOW) Paleozoic groundwater inflow, although periods of increased evaporation during this time may account for zones of less negative isotopic values. The ¹⁸O of this inorganic calcite abruptly shifts to higher values (–6) after 4.5 ka due to the combined effects of increased evaporative enrichment in a closed basin lake and the increased contribution of isotopically high surface water inflow on the hydrologic budget. After 2 ka, the ¹⁸O of the Mg-calcite fluctuates between –13 and –7, implying short-term variability in the lake's hydrologic budget, with values indicating the lake varied from outflow-dominated to evaporation-dominated. The ¹³C values of Mg-calcite remain nearly constant from 8 to 4.5 ka and then trend to higher values upward in the section. This pattern suggests primary productivity in the lake was initially constant but gradually increased after 4.5 ka.This is the sixth in a series of papers published in this issue on the paleolimnology of arid regions. These papers were presented at the Sixth International Palaeolimnology Symposium held 19–21 April, 1993 at the Australian National University, Canberra, Australia. Dr A. R. Chivas served as guest editor for these papers.  相似文献   

A continuous and mechanistic representation of calcite reaction-controlled kinetics in dilute solutions at 25°C and 1 atm total pressure     

Takeshi Arakaki  Alfonso Mucci 《Aquatic Geochemistry》1995,1(1):105-130

  相似文献   

Diurnal Variations of Hydrochemistry in a Travertine-depositing Stream at Baishuitai, Yunnan, SW China   总被引：6，自引：0，他引：6  

Zaihua Liu  Qiang Li  Hailong Sun  Changjun Liao  Huaju Li  Jinliang Wang  Kongyun Wu 《Aquatic Geochemistry》2006,12(2):103-121

Diurnal variations of hydrochemistry were monitored at a spring and two pools in a travertine-depositing stream at Baishuitai, Yunnan, SW China. Water temperature, pH and specific conductivity were measured in intervals of 5 and 30 min for periods of 1 to 2 days. From these data the concentrations of Ca²⁺, HCO₃⁻, calcite saturation index, and CO₂ partial pressure were derived. The measurements in the spring of the stream did not show any diurnal variations in the chemical composition of the water. Diurnal variations, however, were observed in the water of the two travertine pools downstream. In one of them, a rise in temperature (thus more CO₂ degassing) during day time and consumption of CO₂ due to photosynthesis of submerged aquatic plants accelerated deposition of calcite, whereas in the other pool, where aquatic plants flourished and grew out of the water (so photosynthesis was taking place in the atmosphere), the authors suggest that temperature-dependent root respiration underwater took place, which dominated until noon. Consequently, due to the release of CO₂ by the root respiration into water, which dominated CO₂ production by degassing induced by temperature increase, the increased dissolution of calcite was observed. This is the first time anywhere at least in China that the effect of root respiration on diurnal hydrochemical variations has been observed. The finding has implications for sampling strategy within travertine-depositing streams and other similar environments with stagnant water bodies such as estuaries, lakes, reservoirs, pools and wetlands, where aquatic plants may flourish and grow out of water.  相似文献   

碳酸盐岩岩溶作用的元素地球化学表征--以塔河1号的S60井为例   总被引：10，自引：4，他引：10  

钱一雄  蔡立国  李国蓉  刘光祥  韩燕英 《沉积学报》2002,20(1):70-74

通过对塔河地区奥陶系碳酸盐岩及其胶结物方解石的化学成分及方解石晶体微形貌研究后认为 :塔河一号S6 0井埋深 5 433.2 0～ 5 435m发育的岩溶角砾灰岩,属于高度大于 2m的大型古岩溶洞穴沉积;而埋深 5 435m中晶洞中的方解石是地表岩溶带的早中期的淡水与海水的混合带的产物。在本文中,作者指出碳酸盐岩矿物学及地球化学可有效地应用于表生岩溶作用中的深度、强度、期次以及成岩序列及古沉积环境判别等项研究中。  相似文献   

曲边冰洲石的发现及其矿床成因的探讨   总被引：2，自引：0，他引：2  

朱成明  金志升 《矿物学报》1996,16(3):253-256,T002

在各类型冰洲石矿床中发现了大量的冰洲石弯晶，通过冰洲石矿床野外考察的归纳总结，联系到晶体生长和材料力学的有关知识，提出冰州石矿床的成因极可能是原矿床中方解石受到的构造运动强烈影响后，在长期的水淋滤改造作用下发生冰洲石化，并由此而形成冰洲石矿床。  相似文献   

Holocene calcrete crust deposits on the moraine of Batura Glacier, northern Pakistan     

Tetsuya  Waragai 《Island Arc》2005,14(4):368-377

Abstract   Calcretes can be observed on the surface of old moraines around Batura Glacier in the upper Hunza Valley, Karakoram Mountains, Pakistan. They develop as a calcareous crust cementing small gravels under boulders. In order to understand the genesis of the calcrete crust, a variety of methods were employed: (i) study of mineralogy and geochemistry of a calcrete crust precipitated on the lateral moraine using X-ray diffractometer and electron probe microanalysis; (ii) analysis of solute chemistry of surface water and ice bodies around the Batura Glacier; and (iii) accelerator mass spectrometry ¹⁴C dating of the crust itself. The results indicate that the calcrete crust has definite laminated layers composed of a fine-grain and compact calcite layer, and a mineral fragment layer. The chemical composition of the calcite layer is approximately 60% CaO and 1% MgO. The mineral fragment layer consists of rounded grain materials up to 0.2 mm in diameter. It shows a graded bedding structure with fine grains of quartz, albite and muscovite. Meanwhile, as the Paleozoic Pasu limestone is distributed around the terminal of Batura Glacier, Ca cations dissolve in the melt water of the glacier. Accordingly, the calcrete crust is precipitated by decreases in CO₂ partial pressure from glacier ice and evaporation of the melt water, including high concentration of Ca²⁺ at ephemeral streams and small ponds stagnating between the moraine and glacial ice. On the basis of the AMS ¹⁴C age, the calcrete is considered to have formed approximately 8200 calibrated years bp under the Batura glacial stage.  相似文献