海水中超低含量活性磷酸盐的Mg(OH)₂共沉淀法测定研究   总被引：1，自引：0，他引：1       下载免费PDF全文

朱赖民  李犇 《海洋学报》2008,30(3):148-152

活性磷(正磷酸盐)是海洋浮游植物生长所必需的物质基础[1-8],磷的生物可利用性直接影响全球的初级生产力水平.磷在特定的海洋环境中还可能限制固氮作用,成为限制海洋初级生产力的重要因素[1,3,6].海水中磷酸盐含量的测定也是海洋污染调查的重要指标之一[4,9].农业和工业废水中磷的过度排放导致河口和近岸海水富营养化,引起浮游植物异常繁殖,造成“赤潮”现象[4].因此,海水中磷的准确测定对深入理解生物地球化学过程及海洋环境保护具有重要理论和实际意义[4-6,9].磷钼蓝分光光度法是海水中活性磷的经典测定方法,检测限为324 nmo1/dm3[5],但在一些寡营养盐海域,例如在南海、地中海  相似文献   

镁同位素地球化学研究新进展及其应用   总被引：7，自引：3，他引：4  

柯珊  刘盛遨  李王晔  杨蔚  滕方振 《岩石学报》2011,27(2):383-397

作为一种新兴的地质示踪剂,Mg同位素正受到国际地学界日益广泛的关注。Mg同位素地球化学研究已取得了巨大的进展,近期研究工作主要包括两个方面。首先,调查了地球各主要储库和陨石的Mg同位素组成特征,结果表明陨石和地球地幔具有均一并且相似的Mg同位素组成,平均δ²⁶Mg值分别为-0.28±0.06‰和-0.25±0.07‰;相反,上地壳和水圈的Mg同位素组成很不均一,δ²⁶Mg值变化范围分别为-4.84‰~+0.92‰和-2.93‰~+1.13‰。其次,对一些地质和物理化学过程中Mg同位素的分馏行为进行研究,结果表明:(1)地表风化作用可以造成大的Mg同位素分馏,导致重Mg同位素残留在风化产物中而轻Mg同位素进入水圈;(2)岩浆分异过程中Mg同位素平衡分馏很小;(3)高温化学扩散和热扩散过程中Mg同位素会发生显著的动力学分馏。基于这些研究成果,Mg同位素体系已经被初步应用于示踪早期地球形成和壳内物质再循环等过程,并有望在不久的将来应用于示踪大陆地壳的化学演化和地质温度计等研究领域。  相似文献   

How well known are the thermodynamics of Fe–Mg–Ca garnet? Evidence from experimentally determined exchange equilibria     

M. GUIRAUD  R. POWELL 《Journal of Metamorphic Geology》1996,14(1):75-84

ABSTRACT Many thermodynamic calculations relating to metamorphic rocks hinge on the thermodynamic parameters of garnet. Though some models are widely used, it is not clear whether their underlying premise is correct: that a single set of equations can be written for the activities of the end-members of garnet covering the whole compositional range. A voluminous body of data can be used to constrain the thermodynamics of garnet, namely Fe–Mg exchange experimental data involving garnet and another mineral, particularly clinopyroxene, orthopyroxene and olivine. However, examination of these data reveals inconsistencies, apparently stemming from differences between the thermodynamics of low-Ca and high-Ca garnets, with a boundary of about X^g_Ca= 0.15. In the two regions, for the high P–T of the experimental data, the thermodynamics follow the regular model, with values for the interaction parameters in the low Ca region of about w^g_FeMg= 50R and w_aFe–w^g_MgCa=– 1300R, in which R is the gas constant, and in the high Ca region of about w^g_FeMg= 1100R and w^g_CaFe–w^g_MgCa=– 2200R. Using the subregular, rather than the regular, model does not remove the discrepancy. The cause of the discrepancy needs to be identified if reliable calculations on rocks are to be made.  相似文献   

南海北部冷泉碳酸盐岩中钙质生物壳体和自生碳酸盐矿物的Mg/Ca、Sr/Ca及其环境指示     

杨克红  初凤友  朱继浩  马维林  董彦辉 《海洋学报》2014,36(8):39-48

南海北部冷泉碳酸盐岩具有包裹结构和孔洞结构,并且含有丰富的生物遗迹。利用电子探针对位于不同结构单元(包裹结构和基质)的自生碳酸盐矿物和钙质生物壳体进行了Mg/Ca和Sr/Ca分析,结果显示:自生碳酸盐矿物Mg/Ca变化范围为0.50~39.19mmol/mol,平均为12.50mmol/mol,Sr/Ca变化范围为0.06~2.90mmol/mol,平均为0.53mmol/mol;钙质生物壳体Mg/Ca变化范围为1.14~84.57mmol/mol,平均为24.57mmol/mol,Sr/Ca变化范围为0.77~1.84mmol/mol,平均为1.08mmol/mol。Mg/Ca和Sr/Ca的关系显示自生碳酸盐矿物均具有低到中等的Mg/Ca、低Sr/Ca的特征,没有明显分组现象;但是钙质生物壳体却根据其在岩石中的结构位置呈现明显的分组现象,基质钙质生物壳体具有高Mg/Ca、中等Sr/Ca的特征,包裹的钙质生物壳体具有低Mg/Ca、中等Sr/Ca的特征。根据碳酸盐矿物和钙质生物壳体的Mg/Ca特征,认为基质钙质生物壳体是在甲烷渗漏环境下钙化的,无机碳酸盐矿物的出现影响了其Mg/Ca;而包裹的钙质生物壳体是在非甲烷渗漏环境下钙化的,由于生物扰动、灌洗等作用以包裹团块的形式保存在碳酸盐岩中。依据Sr/Ca在成岩过程中的变化特点推测最初形成的基质钙质生物壳体可能具有较现在高的Sr/Ca。研究结果在甲烷渗漏信息地球化学指标提取方面具有一定意义。  相似文献   

Reactivity of dolomitizing fluids and Mg source evaluation of fault-controlled dolomitization at the Benicàssim outcrop analogue (Maestrat basin,E Spain)     

《Marine and Petroleum Geology》2014

The mechanisms responsible for the formation of huge volumes of dolomitized rocks associated with faults are not well understood. We present a case study for high-temperature dolomitization of an Early Cretaceous (Aptian–Albian) ramp in Benicàssim (Maestrat basin, E Spain). In this area, seismic-scale fault-controlled stratabound dolostone bodies extend over several kilometres away from large-scale faults. This work aims at evaluating different Mg sources for dolomitization, estimating the reactivity of dolomitizing fluids at variable temperature and quantifying the required versus available fluid volumes to account for the Benicàssim dolostones. Field relationships, stable ¹³C and ¹⁸O isotopes, as well as radiogenic ⁸⁷Sr/⁸⁶Sr isotopes, indicate that dolomitization at Benicàssim was produced by a high-temperature fluid (>80 °C). ¹³C and ¹⁸O isotopic compositions for dolomite vary from +0.5 to +2.9‰ V-PDB and from +21.1 to +24.3 V-SMOW, respectively. A Mg source analysis reveals that the most likely dolomitizing fluid was seawater-derived brine that interacted with underlying Triassic red beds and the Paleozoic basement. Geochemical models suggest that evolved seawater can be considerably more reactive than high-salinity brines, and the maximum reactivity occurs at about 100 °C. Mass-balance calculations indicate that interstitial fluids with high pressure and/or high temperature relative to the normal geothermal gradient cannot account for the volume of dolomite at Benicàssim. Instead a pervasive fluid circulation mechanism, like thermal convection, is required to provide a sufficient volume of dolomitizing fluid, which most likely occurred during the Late Cretaceous post-rift stage of the Maestrat basin. This study illustrates the importance of fluid budget quantification to critically evaluate genetic models for dolomitization and other diagenetic processes.  相似文献   

印-太暖池区全新世Mg/Ca温度转换中的盐度因素          下载免费PDF全文

王文洁  徐建 《热带海洋学报》2014,33(2):94-100

有孔虫Mg/Ca温度计是古海洋学研究中恢复古温度的重要手段之一。然而,越来越多的研究表明,Mg/Ca温度计的准确性受多种因素的影响,特别是盐度的控制十分重要。文章实测并搜集整理了印-太暖池地区全新世(大约11kaB.P.以来)1000余个浮游有孔虫Mg/Ca比值数据,分别利用包含和不包含盐度信息的两个常用转换方程求取了古海水温度,并将二者进行了对比,旨在探讨盐度因素对Mg/Ca温度计的影响。结果显示,在表层水温大约28℃以下,两个方程获得的结果几乎一致,平均差异为0.07℃;在表层水温28℃以上,二者平均相差大约1℃。此外,表层海水盐度越低,包含盐度信息的转换方程获得的古海水氧同位素的值越大。上述结果揭示盐度对该地区有孔虫Mg/Ca比值的影响效应不明显。  相似文献   

白令海底栖有孔虫壳体镁钙比值对水团温度的响应     

叶黎明  邱中炎  雷吉江 《海洋地质与第四纪地质》2012,(4):165-170

底栖有孔虫壳体Mg/Ca是重建深层水团古温度的主要指标。通过分析表层沉积物样品中底栖有孔虫Uvigerina peregrina壳体的Mg/Ca和δ18 O,探讨了"Mg/Ca古温度重建方法"在白令海低温水体中的可行性及其转换函数。结果表明,利用U.peregrina壳体δ18 O换算的"结壳温度"明显低于"现代水团温度",不能客观反映温度对Mg/Ca的控制作用;可能受季节性变化的影响,水深小于150m样品中U.peregrina壳体的Mg/Ca与"现代水团温度"之间并没有表现出明显的相关性,但是,在深海区两者之间却呈现出良好的指数关系:Mg/Ca=0.69*e0.43*T。该公式指出白令海低温水体中Mg/Ca对温度的敏感性约为43%℃-1,由其估算的温度误差约为0.2℃。  相似文献   

广西横县六景中泥盆统Mg、Ca、Na、Sr、δ13C和δ18O化学地层学特征     

刘疆  白志强 《物探与化探》2009,33(4)

广西横县六景中泥盆统的Mg、Ca、Sr、Na、δ13C和δ18O化学地层特征清晰地量化了该剖面的岩相及其变化规律,并在生物地层框架内,使该剖面的高精度划分和高精度区域性对比成为可能.化学地层数据与该剖面的沉积相和生物相之间存在良好的对应关系,显示那叫期的中泥盆统段为滩后泻湖与蒸发滩3次交替沉积环境;民塘期至谷闭初期为碳酸盐礁滩后斜坡沉积环境.那叫组白云岩的化学地层数据显示不能简单排除白云岩的化学地层学研究价值,可以对成岩作用较弱的细晶、粉晶白云岩,尤其薄层、纹层白云岩开展适度的化学地层学研究.  相似文献   

The local structure of Ca-Na pyroxenes. II. XANES studies at the Mg and Al K edges     

A. Mottana  T. Murata  A. Marcelli  Z. Y. Wu  G. Cibin  E. Paris  G. Giuli 《Physics and Chemistry of Minerals》1999,27(1):20-33

X-ray absorption spectra at the Mg and Al K edges have been recorded using synchrotron radiation on synthetic end member diopside (Di) and jadeite (Jd) and on a series of natural Fe-poor Ca-Na clinopyroxenes compositionally straddling the Jd-Di join. The spectra of C2/c end members and intermediate members of the solid solution series (C-omphacites) are different from those of the intermediate members having P2/n symmetry (P-omphacites). Differences can be interpreted and explained by comparing the experimental spectra with theoretical spectra calculated via the full multiple-scattering formalism, starting from the atomic positional parameters determined by single-crystal X-ray diffraction structure refinement on the same samples. Atomic clusters with at least 89 atoms, extending to more than 0.60 nm away from the Mg or Al absorbers, are needed to reproduce the experimental spectra. This shows that in the clinopyroxene systems XANES detects medium- rather than short-range order-disorder relationships. Theoretical spectra match the experimental ones well for all features in the regions from 16 to 60 eV above threshold. Experimental near-edge features in the first 16 eV are also reproduced, albeit less accurately. Certain near-edge features of C-omphacites reflect the octahedral arrangement of the back-scattering six O atoms nearest neighbours of the probed atom (Mg or Al) located at site M1 of the crystal structure, thus being indicators of short-range order. Others arise again from medium-range order. P-omphacites show more complicated spectra than C-omphacites. Their additional features reflect the increased complexity of the structure and the greater local disorder around the probed atom induced by the two alternative M1, M11 configurations of the six O atoms forming the first coordination shells. Mg and Al are confirmed to be preferentially partitioned in the M1 and M11 site of the P-omphacite crystal structure, however with a certain degree of local disorder. The relative heights of certain prominent features are directly related to sample composition in terms of Di:Jd ratio in the Al K-edge spectra, whereas they show abrupt variations in the Mg K-edge spectra. They demonstrate that XANES is directly related to composition and may be used to distinguish C- from P-omphacites. Received: 24 November 1998 / Revised, accepted: 10 June 1999  相似文献   

Geochemical fingerprints of dolomitization in Bahamian carbonates: Evidence from sulphur,calcium, magnesium and clumped isotopes     

Sean T. Murray  John A. Higgins  Chris Holmden  Chaojin Lu  Peter K. Swart 《Sedimentology》2021,68(1):1-29

In an effort to constrain the mechanism of dolomitization in Neogene dolomites in the Bahamas and improve understanding of the use of chemostratigraphic tracers in shallow‐water carbonate sediments the δ³⁴S, Δ₄₇, δ¹³C, δ¹⁸O, δ^44/40Ca and δ²⁶Mg values and Sr concentrations have been measured in dolomitized intervals from the Clino core, drilled on the margin of Great Bahama Bank and two other cores (Unda and San Salvador) in the Bahamas. The Unda and San Salvador cores have massively dolomitized intervals that have carbonate associated sulphate δ³⁴S values similar to those found in contemporaneous seawater and δ^44/40Ca, δ²⁶Mg values, Sr contents and Δ₄₇ temperatures (25 to 30°C) indicating relatively shallow dolomitization in a fluid‐buffered system. In contrast, dolomitized intervals in the Clino core have elevated values of carbonate associated sulphate δ³⁴S values indicating dolomitization in a more sediment‐buffered diagenetic system where bacterial sulphate reduction enriches the residual in ³⁴S, consistent with high sediment Sr concentrations and low δ^44/40Ca and high δ²⁶Mg values. Only dolomites associated with hardgrounds in the Clino core have carbonate associated δ³⁴S values similar to seawater, indicating continuous flushing of the upper layers of the sediment by seawater during sedimentary hiatuses. This interpretation is supported by changes to more positive δ^44/40Ca values at hardground surfaces. All dolomites, whether they formed in an open fluid‐buffered or closed sediment‐buffered diagenetic system have similar δ²⁶Mg values suggesting that the HMC transformed to dolomite. The clumped isotope derived temperatures in the dolomitized intervals in Clino yield temperatures that are higher than normal, possibly indicating a kinetic isotope effect on dolomite Δ₄₇ values associated with carbonate formation through bacterial sulphate reduction. The findings of this study highlight the utility of applying multiple geochemical proxies to disentangle the diagenetic history of shallow‐water carbonate sediments and caution against simple interpretations of stratigraphic variability in these geochemical proxies as indicating changes in the global geochemical cycling of these elements in seawater.  相似文献