Factors Controlling Sulfide Geochemistry in Sub-tropical Estuarine and Bay Sediments     

John W. Morse  Heather Thomson  David W. Finneran 《Aquatic Geochemistry》2007,13(2):143-156

The primary factors that control the concentration of total reduced (inorganic) sulfide in coastal sediments are believed to be the availability of reactive iron, dissolved sulfate and metabolizable organic carbon. We selected nine sites in shallow (<3 m), close to sub-tropical, estuaries and bays along the central Texas coast that represented a range in sediment grain size (a proxy for reactive iron), salinity (a proxy for dissolved sulfate), and total organic carbon (a proxy for metabolizable organic carbon). Based on these parameters a prediction was made of which factor was likely to control total reduced sulfide at each site and what the relative total reduced sulfide concentration was likely to be. To test the prediction, the sediments were analyzed for total reduced sulfide, acid volatile sulfide, and citrate dithionate-extractable, HCl-extractable and total Fe in the solid phase. Using solid-state gold–mercury amalgam microelectrodes and voltammetry, we determined pore water depth profiles of Fe(II) and ΣH₂S and presence or absence of FeS_(aq). At five of the nine sites the calculated degree of sufildization of citrate dithionite-reactive-iron was close to or greater than 1 indicating that rapidly reactive iron was probably the limiting factor for iron sulfide mineral formation. At one site (salinity = 0.9) dissolved Fe(II) was high, ΣH₂S was undetectable and the total reduced sulfide concentration was low indicating sulfate limitation. At the last three sites a low degree of sulfidization and modest total reduced (inorganic) sulfide concentrations appeared to be the result of a limited supply of metabolizable organic carbon. Fe(II)–S(-II) clusters (FeS_(aq)) were undetectable in 10 out of 12 bay sediment profiles where ΣH₂S was close to or below detection limits, but was observed in all other porewater profiles. Acid volatile sulfide, but not total reduced sulfide, was well correlated with total organic carbon and ranged from being undetectable in some cores to representing a major portion of total reduced sulfide in other cores. Although predicted controls on total reduced sulfide were good for very low salinity water or sandy sediments, they were only right about half the time for the other sediments. The likely reasons for the wrong predictions are the poor correlation of total organic carbon with grain size and differing fractions of metabolizable organic carbon in different sedimentary environments. Differences in sediment accumulation rates may also play a role, but these are difficult to determine in this region where hurricanes often resuspend and move sediments. This study demonstrates the need to examine more complex and often difficult to determine parameters in anoxic “normal marine” sediments if we are to understand what controls the concentration and distribution of sulfides.  相似文献   

蓝藻聚铁作用的模拟实验   总被引：3，自引：0，他引：3       下载免费PDF全文

刘志礼  杜汝霖 《地质科学》1993,28(1):79-86

实验模拟前寒武纪大气的高二氧化碳分压(P_CO2),低氧浓度条件下,加入较低浓度(6μg/g)铁的Zarronk培养液培养蓝藻Spirulina platensis,观察铁的沉淀与凝聚。藻在生长过程中不断改变环境的离子平衡系统以及pH,Eh等,造成铁的氧化、还原、络合和Fe³⁺沉淀。实验组与未加蓝藻的对照组有显著差别。实验证实藻在聚铁和铁矿形成中起重要作用。  相似文献   

Photochemical degradation of organic iron complexing ligands in seawater     

Rodney?T.?PowellEmail author  Amy?Wilson-Finelli 《Aquatic Sciences - Research Across Boundaries》2003,65(4):367-374

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The role of coarse colloids as a carrier phase for trace metals in riverine systems   总被引：2，自引：0，他引：2  

Davide Vignati  Janusz Dominik 《Aquatic Sciences - Research Across Boundaries》2003,65(2):129-142

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Sequential extraction procedure in columns—part 2: application of a new method     

F.?WisotzkyEmail author  N.?Cremer 《Environmental Geology》2003,44(7):805-810

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Size Fractionation (Dissolved, Colloidal and Particulate) of Trace Metals in the Thur River, Switzerland     

Laura Sigg  Hanbin Xue  David Kistler  René Sshönenberger 《Aquatic Geochemistry》2000,6(4):413-434

The distribution of some trace metals (Cu, Zn, Ni, Co,Fe, Mn) and of DOC over a particulate (> 1 m),a colloidal (size < 0.45 m and molecular weight > 10 kD) and an ultrafiltered fraction (< 10 kD)was determined at several sites on the Thur River,Switzerland, at various times of the year. Thecomplexation of Cu by strong ligands in theultrafiltrate and in the conventional filtrate (<0.45 m) was compared using a ligand-exchange/CSV method.The <0.45 m concentrations of Cu (from anaverage of 7 nM to 24 nM), Zn (<5–23 nM), Ni (5–13 nM),Co (1.5–3 nM) and Mn (7–92 nM)increased downstream. The major part of Cu, Zn, Niand Co usually occurred in the ultrafiltratefraction at all sites, whereas Fe and Mn were mostlyin the particulate fraction, under conditions of lowsuspended matter content (< 10 mg L^-1) in theriver. The percentage of metal in the colloidalfraction, with respect to the 0.45-m filtrate,decreased in the order: Cu (median 11%) > Zn Ni(median 5–6%) > Mn Co (median < 5%). DOCalso consisted mostly of molecules in the < 10 kDrange.Cu was strongly complexed by natural organic ligandsin all filtrate and ultrafiltrate samples. A largepart of the strong Cu binding ligands consisted ofcompounds in the < 10 kD range, but colloidalligands with similar properties also occurred. Cu wasdistributed among the dissolved and the colloidalligands, roughly in proportion to organic carbon.The colloidal fraction (as defined here) did notincrease in its proportional amount downstream and wasonly of limited significance in transporting traceelements in the Thur River under low discharge conditions.  相似文献   

Reappraisal of the structure of the Western Iron Ore Group, Singhbhum craton, eastern India: Implications for the exploration of BIF-hosted iron ore deposits   总被引：1，自引：0，他引：1  

Gautam Ghosh  Joydip Mukhopadhyay 《Gondwana Research》2007,12(4):525-532

The middle to late Archean Iron Ore Group rocks occurring along the western margin (the Western Iron Ore basin) of the Singhbhum Granite massif in the Singhbhum craton were deformed during Iron Ore orogeny and are disposed in a horseshoe-shaped synclinal structure in the eastern part of the Indian shield. The Western Iron Ore basin hosts almost all the major high-grade iron ore deposits of eastern India. Contrary to the established view, present analysis emphasizes that the horseshoe fold in reality is a synclinorium consisting of a syncline–anticline fold pair which were later cross-folded along an east–west axis.

Structural analysis in the eastern anticline of the ‘horseshoe synclinorium’ suggests that the BIF hosting the high-grade iron ore bodies are disposed in three linear NNE–SSW trending belts, each showing an open synclinal geometry. Later cross folding produced development of widespread dome and basin pattern at the sub-horizontal hinge zones of these synclinal fold belts. The major iron ore deposits in the eastern anticline at the present level of erosion are preferentially localized within shallow elongated basinal structures only. The axis of the adjoining western syncline was similarly uplifted as partial culminations where cross-folded against E–W anticlinal axes. But here, the BIF-iron ore bodies are preferentially localized within elongated domal structures in contrast to the basinal sites in the adjacent eastern anticline. Such an inference based on structural analysis could probably be utilized as a potential tool for all future explorations, reserve estimation and recovery of the iron ore deposits in the terrain.  相似文献   

Solubility of FeO in (Mg,Fe)SiO₃ perovskite and the post-perovskite phase transition     

Shigehiko Tateno  Kei Hirose  Nagayoshi Sata  Yasuo Ohishi 《Physics of the Earth and Planetary Interiors》2007,160(3-4):319-325

Phase relations in Mg_0.5Fe_0.5SiO₃ and Mg_0.25Fe_0.75SiO₃ were investigated in a pressure range from 72 to 123 GPa on the basis of synchrotron X-ray diffraction measurements in situ at high-pressure and -temperature in a laser-heated diamond-anvil cell (LHDAC). Results demonstrate that Mg_0.5Fe_0.5SiO₃ perovskite is formed as a single phase at 85–108 GPa and 1800–2330 K, indicating a high solubility of FeO in (Mg,Fe)SiO₃ perovskite at high pressures. Post-perovskite appears coexisting with perovskite in Mg_0.5Fe_0.5SiO₃ above 106 GPa at 1410 K, the condition very close to the post-perovskite phase transition boundary in pure MgSiO₃. The coexistence of perovskite and post-perovskite was observed to 123 GPa. In addition, post-perovskite was formed coexisting with perovskite also in Mg_0.25Fe_0.75SiO₃ bulk composition at 106–123 GPa. In contrast to earlier experimental and theoretical studies, these results show that incorporation of FeO stabilizes perovskite at higher pressures. This could be due to a larger ionic radius of Fe²⁺ ion, which is incompatible with a small Mg²⁺ site in the post-perovskite phase.  相似文献   

辽宁弓长岭一矿区铁矿石品位分布的地质统计学研究     

李莲花  李卉 《国土资源》1998,(2)

弓长岭铁矿地质条件复杂,使矿山生产长期受到制约。运用地质统计学的方法对该矿区的ＴＦｅ,ＦｅＯ品位分布规律进行了系统研究,确定了品位分布的结构模型,对今后矿山开发和生产提出了建议。  相似文献   

Analytical perspective on trace element species of interest in exploration   总被引：1，自引：0，他引：1  

Gwendy E. M. Hall 《Journal of Geochemical Exploration》1998,61(1-3)

Analysis of soil and sediment samples, using selective extraction methods to distinguish different phases, is of particular interest in exploration geochemistry to locate deeply buried mineral deposits. There are various mechanisms of binding labile elements in the secondary environment, including physical and chemical sorption, precipitation, chelation and complexation. Phases present in soils and sediments which are likely to scavenge ‘free' elements include amorphous Mn and Fe oxides, the humic and fulvic components of humus, and clays. This paper reviews these forms of trace elements and the methods in current use to quantify them. Examples of precision data, both for control and survey samples, are given with respect to trace elements dissolved from the ‘soluble organic' component of humus, Mn oxides and amorphous Fe oxides. The high sensitivity of inductively coupled plasma mass spectrometry (ICP–MS) is required to measure accurately and precisely a large suite of trace elements, especially where only small fractions of elements are dissolved by such leaches as the commercially available Enzyme and MMI (Mobile Metal Ion) extractions. The relative standard deviations (RSD) obtained for 33 elements (e.g. Ag, Cd, In, I) in the standard reference sample (SRM), TILL-2, are in the range 0.5–8% for the hydroxylamine hydrochloride (NH₂OH·HCl) leach designed to extract hydrous Fe and Mn oxides. The corresponding RSDs for elements in the reactive Mn oxide phase extracted by the Enzyme leach are in the range 3–19% except for some trace elements at levels close to detection limit (e.g. Cd, Bi). The RSDs obtained for field duplicates are inferior to those for analytical replicates (i.e. sample splits), probably a reflection of different concentrations of the host phase. In one soil survey, the Fe extracted by a 0.25 M NH₂OH·HCl leach ranged conservatively from 0.2 to 1.7% whereas the Mn extracted by the Enzyme leach varied extensively, from 0.3 to >999 ppm. In contrast, precision, at 1–7% RSD, for field duplicates was found to be comparable with that for both analytical duplicates and the SRM, LKSD-4, for elements associated with the humic and fulvic component of humus samples sieved to <177 μm.  相似文献