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1.
内蒙古查干诺尔盐湖晚更新世至全新世孢粉植物群与古气候 总被引：1，自引：0，他引：1
本文基于内蒙古二连盆地查干诺尔盐湖８３－ＣＫ１井岩芯样品孢粉分析结果，将孢粉谱划分为Ⅰ，Ⅱ，Ⅲ，Ⅳ四个孢粉带；根据孢粉组合特征讨论了晚更新世晚期以来研究区植被发展和气候演变以及盐湖沉积形成环境等问题。８３－ＣＫ１井沉积剖面年龄根据＾１４Ｃ测定。研究结果表明，晚更新世晚期和全新世早期气候相对温暖湿润，为盐类矿床形成的预备阶段；晚更新世末期和全新世晚期气候干燥寒冷，是内蒙古盐湖的主要成盐期。 相似文献
2.
天目山姚砂岭地区第四纪沉积环境研究 总被引：7，自引：1，他引：7
根据对天目山姚砂岭剖面样品的分析得出下述结论：１．粒度参数和ＣＭ图象反映该处沉积物Ｃ值均在０Φ以上，多属于滚动悬浮搬运，应属于洪积和冲积相。２．Ｆｅ＾３＋／Ｆｅ＾２＋测定表明，该区和第四纪期间最低年均气温并未低于０℃，因此不具备冰川发育的条件。３．该剖面样品氧化物有以ＡＬ２Ｏ３和Ｆｅ２Ｏ３为主的富铝铁化现象，表明本区第四纪主要经历了温暖湿润的化学风环境。４．重矿和扫描电镜分析发现，锆石具有气、液包 相似文献
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催化动力学光度法测定痕量铁的研究 总被引：2，自引：0，他引：2
研究了在ｐＨ８．５的Ｎａ２Ｂ４Ｏ７－ＨＣｌ介质中,Ｆｅ＾３＋催化Ｈ２Ｏ２氧化茜素红褪色,建立了动力学光度法测定痕量Ｆｅ＾３＋的方法。方法检出限０．０４３μｇ／ｍｌ,线性范围０￣０．１７μｇ／ｍｌ,除Ｍｎ＾２＋、Ｃｏ＾２＋等离子外,其余共存离子基本无干扰,实测了天然水和化学试剂中痕量Ｆｅ＾３＋,结果满意。 相似文献
5.
苏州澄湖SC1孔晚更新世晚期以来的古环境演变研究 总被引：1，自引：1，他引：0
通过对苏州澄湖SC1孔沉积物的粒度、磁化率、孢粉和有孔虫等的实验分析,并结合沉积物的岩性构造特征以及AMS 14C测年数据,探讨了晚更新世晚期以来苏州澄湖地区的气候波动特征以及海侵、海退沉积巡回序列。研究发现该区域气候与世界气候波动性一致,具有温暖湿润-冷而略干-温暖湿润-暖热潮湿-温凉略干-温暖湿润的波动变化特征;晚更新世晚期以来具有两个海相沉积地层,一为晚更新世晚期海侵(约为34 kaBP),另一为全新世中期海侵(（6 955±50）aBP);整个剖面缺失硬粘土层,与之对应的则是两海相地层之间的泥砂互层;沉积环境经历了晚更新世晚期海侵期河床、河漫滩相-末次冰期干冷期河流湖沼相-全新世早期河口湾亚相-全新世中期滨浅海相-全新世晚期淡水湖沼相的演变过程。 相似文献
6.
氢化物—原子荧光法测定岩石中痕量硒的干扰及消除 总被引：12，自引：10，他引：12
用ＨＦ－ＨＣｌＯ４－ＨＮＯ３混合酸分解样品，采用Ｆｅ＾３＋作释放剂，研究了不同量的Ｆｅ＾３＋与ＨＣｌ酸度对Ｓｅ荧光强度的影响和干扰离子消除的效果，以及Ｆｅ＾３＋存在Ｔｅ存在下对Ｓｅ测定的影响。方法的检出限为０．０１μｇ／ｇ．样品中Ｓｅ量为０．１μｇ／ｇ的相对标准偏差（ｎ＝１１）是５．４％。用于岩石标样中痕量Ｓｅ的测定，结果较好。 相似文献
7.
对江汉盆地Ｔ油田主要的工业储层－下第三系新光沟嘴组沉积岩石的成岩流体进行了热力学研究。实测的成岩矿物流体包裹体的均一温度为１１０－１３９℃，属于该区中成岩阶段的温度范围（６７－１５５℃）。成岩流体的压力为１０．２－５６ＭＰａ。成岩流体中阳离子的活度出现Ｃａ＾２＋＞Ｍｇ＾２＋＞Ｎａ＾＋＞Ｋ＾＋＞Ｆｅ＾３＋＞Ｆｅ＾２＋；阴离子的活离出现ＨＣＯ３＾－＞ＳＯ４＾２－＞Ｆ＾－＞Ｃｌ＾－＞ＣＯ３＾２－；气相成 相似文献
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含铁绿柱石的改色机制研究 总被引：7，自引：0，他引：7
含铁绿柱石经γ射线辐照或特定温度热处理,可因铁价态的改变引起颜色发生相应变化。处理前后的吸收光谱和顺磁共振谱研究表明,辐作用使隧道位的Ｆｅ＾２＋氧化Ｆｅ％３＋,八一位上的Ｆｅ＾３＋还原为Ｆｅ＾２＋,热处理使隧道位及八面体位Ｆｅ＾３＋均还原为Ｆｅ＾２＋。 相似文献
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A comparative study of blue and green beryl crystals (from the region of Governador Valadares, Minas Gerais, Brazil) using electron paramagnetic resonance (EPR) and optical absorption (OA) spectroscopy is reported. The EPR spectra show that Fe3+ in blue beryl occupies a substitutional Al3+ site and in green beryl is localized in the structural channels between two O6 planes. On the other hand the infrared spectra show that the alkali content in the blue beryl is mostly at substitutional and/or interstitial sites and in green beryl is mostly in the structural channels. The OA spectra show two types of Fe2+. Thermal treatments above 200° C in green beryl cause the reduction of Fe3+ into Fe2+ accompanied by a change of color to blue. The blue beryl color does not change on heating. The kinetics of the thermal conversion of Fe3+ into Fe2+ is composed of two first order processes; the first one has an activation energy ΔE 1=0.30 eV and the second one has an activation energy ΔE 2=0.46 eV. 相似文献
12.
X-ray absorption spectroscopy, including extended X-ray absorption fine structure (EXAFS) and X-ray absorption near-edge structure (XANES) techniques, have been used to determine the structure and speciation of complexes for Fe2+ and Fe3+ chloride solutions at a variety of pH's, ionic strengths, and chloride/iron ratios.Low intensity K-edge transition features and analysis of modified pair correlation functions, derived from Fourier transformation of EXAFS spectra, show a regular octahedral coordination of Fe(II) by water molecules with a first-shell Fe2+-O bond distance, closely matching octahedral Fe2+-O bonds obtained from solid oxide model compounds. Solution Fe2+-O bond distances decrease with chloride/iron ratio, pH, and total FeCl2 concentration. A slight intensification of the transition with increasing FeCl2 concentration suggests that chloride may begin to mix with water as a nearest-neighbor octahedral ligand. Fe3+ solutions show a pronounced increase in the transition intensities between 1.0 M FeCl3/7.8 M Cl? to 1.0 M FeCl3/ 15 M Cl?, indicating a coordination change from octahedral to tetrahedral complexes. EXAFS analyses of these solutions show an increase in first-shell Fe3+-ligand distances despite this apparent reduction in coordination number. This can be best explained by a change from regular octahedral complexes of ferric iron (either Fe(H2O)63+ or trans-Fe(H2O)4Cl2 or both; Fe3+-O bond distances of 2.10 Å) to tetra-chloro complexes [Fe3+-Cl bond distances of 2.25 Å]. 相似文献
13.
Fernando Barra Fernando Gervilla Elkin Hernández Martin Reich José Alberto Padrón-Navarta José Maria González-Jiménez 《Mineralogy and Petrology》2014,108(6):819-836
La Cabaña peridotite is part of a dismembered ophiolite complex located within the metamorphic basement of the Coastal Cordillera of south-central Chile, and is the only location in Chile were Cr-spinels have been described so far. The La Cabaña peridotite is part of the Western Series unit, which comprises meta-sedimentary rocks, metabasites, and serpentinized ultramafic rocks. This unit has been affected by greenschist-facies metamorphism with reported peak PT conditions of 7.0–9.3 kbar and 380°–420 °C. Within La Cabaña peridotite Cr-spinels are present in two localities: Lavanderos and Centinela Bajo. In Lavanderos, Cr-spinel occurs in small chromitite pods and as accessory/disseminated grains with a porous or spongy texture in serpentinite, whereas in Centinela Bajo Cr-spinel is present as accessory zoned grains in partly serpentinized dunites, and in chromitite blocks. All Cr-spinels display variable degrees of alteration to Fe2+-rich chromite with a variation trend of major elements from chromite to Fe2+-rich chromite similar to those observed in other locations, i.e., an increase in Fe2O3 and FeO, a decrease in Al2O3 and MgO. Cr2O3 content increases from chromite to Fe2+-rich chromite in chromitite pods from Lavanderos and chromitite blocks from Centinela Bajo, but decreases in ferrian chromite zones in accessory grains from Centinela Bajo. The minor element (Ti, V, Zn, Ni) content is mostly low and does not exceed 0.4 wt.%, with the exception of MnO (<0.9 wt.%), which shows a correspondence with increasing degree of alteration. Cr# (Cr/Cr?+?Al) versus Mg# (Mg/Mg?+?Fe2+) and Fe3+/Fe3++Fe2+ versus Mg# plots are used to illustrate the Cr-spinel alteration process. Overall, the Cr-spinels from Lavanderos (chromitite pods and disseminated grains) exhibit Cr# values ranging from 0.6 to 1.0, Mg# (Mg/Mg?+?Fe2+) below 0.5, and (Fe3+/Fe3++Fe2+) <0.4. Cr-spinels from chromitites in Centinela Bajo have Cr# and Mg# values that range from 0.65 to 1.0, and 0.7-0.3, respectively, and (Fe3+/Fe3++Fe2+)?3+/Fe3++Fe2+) ratio is less than 0.4 in chromite cores and Fe2+-rich chromite, and >0.5 in ferrian chromite and Cr-magnetite. Interpretation of the data obtained and Cr-spinel textures indicate that the alteration of Cr-spinel is a progressive process that involves in its initial stages the reaction of chromite with olivine under water-saturated conditions to produce clinochlore and Fe2+-rich chromite. During this stage the chromite can also incorporate Ni, Mn, and/or Zn from the serpentinization fluids. As alteration progresses, Fe2+-rich chromite loses mass resulting in the development of a spongy texture. In a later stage and under more oxidizing conditions Fe3+ is incorporated in chromite/Fe2+-rich chromite shifting its composition to an Fe3+-rich chromite (i.e., ferrian chromite). Depending on the fluid/rock and Cr-spinel/silicate ratios, Cr-magnetite can also form over Fe2+-rich chromite and/or ferrian chromite as a secondary overgrowth. The compositional changes observed in Cr-spinels from La Cabaña reflect the initial stages of alteration under serpentinization conditions. Results from this study show that the alteration of Cr-spinels is dependent on temperature. The degree and extent of alteration (formation of Fe2+-rich and/or ferrian chromite) are controlled by the redox nature of the fluids, the Cr-spinel/silicate and the fluid/rock ratios. 相似文献
14.
I. A. Baksheev O. Yu. Plotinskaya V. O. Yapaskurt M. F. Vigasina I. A. Bryzgalov E. O. Groznova L. I. Marushchenko 《Geology of Ore Deposits》2012,54(6):458-473
Tourmalines from the Kalinovka porphyry copper deposit with epithermal bismuth-gold-basemetal mineralization and the Michurino gold-silver-base-metal prospect have been studied in the South Urals. Tourmaline from the Kalinovka deposit occurs as pockets and veinlets in quartz-sericite metasomatic rock and propylite. The early schorl-“oxy-schorl” [Fetot/(Fetot + Mg) = 0.66?0.81] enriched in Fe3+ is characterized by the homovalent isomorphic substitution of Fe3+ for Al typical of propylites at porphyry copper deposits. The overgrowing tourmalines of the second and third generations from propylite and quartz-sericite metasomatic rock are intermediate members of the dravite-magnesio-foitite solid solution series [Fetot/(Fetot + Mg) = 0.05?0.46] with homovalent substitution of Mg for Fe2+ and coupled substitution of X ? + YAl for XNa + YMg. These substitutions differ from the coupled substitution of YAl + WO2? for YFe2+ + WOH? in tourmaline from quartz-sericite rocks at porphyry copper deposits. At the Michurino prospect, the tourmaline hosted in the chlorite-pyrite-quartz veins and veinlets with Ag-Au-Cu-Pb-Zn mineralization is an intermediate member of the dravite-magnesio-foitite solid solution series [Fetot/(Fetot + Mg) = 0.20?0.31] with homovalent substitution of Mg for Fe2+ and coupled substitutions of X ? + YAl for XNa + YMg identical to that of late tourmaline at the Kalinovka deposit. Thus, tourmalines of the porphyry and epithermal stages are different in isomorphic substitutions, which allow us to consider tourmaline as an indicator of super- or juxtaposed mineralization. 相似文献
15.
Crystal chemistry of Fe-containing sphalerites 总被引：2，自引：0，他引：2
Cell dimensions and solvus properties of Fe-containing sphalerites, depending on temperature and sulfur fugacity, were investigated
using equilibrated powdered materials synthesized from elements and binary sulfides under vacuum. The Fe solvus in sphalerite,
determined by optical microscopy and microprobe analysis, are directly correlated with increasing temperature and decreasing
sulfur fugacity controlled by solid-state buffers. The increase of lattice parameters with Fe correlates with an increase
of FeS independent of sulfur fugacity up to 10 mol% FeS within ZnS. Above about 10 mol% the lattice parameters are strongly
depending on the sulfur fugacity controlled Fe3+/Fe2+ ratios. The Fe3+/Fe2+ ratios determined by Moessbauer spectroscopy and involving metal vacancies depend on the sulfur fugacity. The critical Fe2+ content determined by experimental simulations as well as the minimal Fe3+/ Fe2+ ratios agree with the required minimal Fe content for CuFeS2-DIS in sphalerite. The critical Fe2+ content also agrees with the change of Moessbauer signal from a singlet to a doublet for Fe2+ containing sphalerite. Pyrrhotite exsolutions in sphalerite caused by higher sulfur fugacity show orientationally intergrown
with the sphalerite matrix. Density data calculated from lattice parameters and composition are compared with experimental
density measurements.
Received: 25 April 2001 / Accepted: 14 February 2003 相似文献
16.
The analysis of available data on the Fe3+/Fe2+ ratio of impact-produced glasses showed that tektites and some other types of impact glasses are reduced compared with the precursor target material. Possible reasons for the change in the degree of iron oxidation in the impact process are still debatable. Based on the analysis of redox reactions in relatively simple systems with iron in different oxidation states (Fe-O and SiO2-FeO-Fe2O3) and the available data on the influence of temperature, oxygen partial pressure (pO2), and total pressure (P tot) on the Fe3+/Fe2+ ratio of silicate melts, a model was proposed suggesting that the lower Fe3+/Fe2+ values of tektites formed in the impact process compared with the initial target material could be related to the characteristics of oxygen regime during the decompression stage following shock compression. One of the main prerequisites for the occurrence of reduction reactions involving iron and other elements is the attainment of high temperatures (>1800–2000°C) at a certain stage of decompression, providing the complete melting and partial evaporation of the material. When the vapor pressure in the system becomes equal to the total pressure during adiabatic decompression, a further decrease in P tot will be inevitably accompanied by a decrease in pO2 and, correspondingly, partial reduction of Fe3+ to Fe2+ in the melt. The reactions of decompression reduction occur under closed-system conditions and do not require oxygen removal from the system. The higher the temperature and Fe3+/Fe2+ ratio of the melt, the more extensive iron reduction can be observed during the final stages of decompression. If the temperatures attained during decompression after an impact event are sufficient (>2500–3000°C) for the complete evaporation of the material, the melt produced during subsequent condensation must be significantly more reduced than the initial material. The final stage of the impact process is characterized by a catastrophic expansion of the explosion cloud, condensation, and rapid cooling. During this stage, the system is already not closed. The quenched glasses of this stage record the redox state of earlier melts. In addition, they can contain microinclusions of the products of nonequilibrium vapor condensation with iron compounds of different oxidation states, including metallic iron and iron oxides (wüstite, magnetite, and hematite). 相似文献
17.
Ilvaite samples from six different localities in Japan are found to be members of a solid-solution series varying from Ca(Fe2+,Fe3+)2Fe2+(OH)O Si2O7 to approaximately Ca(Fe2+,Fe3+)2Fe 0.5 2+ Mn 0.5 2+ (OH)O Si2O7, and have been studied by Mössbauer spectrometry and magnetic measurements. The variation in intensity of Mössbauer doublets confirms that Mn substitutes for Fe2+ in the M(B) cation site. An temperatures decreasing from 300 K to 4K, an abrupt change in the reciprocal mass magnetic susceptibility, 1/x g, occurs about 120 K; 1/x g depends linearly upon temperature above 120 K. This change, which is characterized by an unusual mode of decrease in 1/x g, has been interpreted based on Mössbauer spectra at 80 K: the spectra of Fe2+ and Fe3+ in the M(A) site show Zeeman splitting, whereas those of Fe2+ in the M(B) site do not show the effect. This Mössbauer evidence suggests that magnetic spins of Fe in M(A) are in an ordered state, very likely of antiparallel coupling, whereas those of Fe in M(B) are randomly oriented, showing that below 120 K ilvaite has two different magnetic states for Fe ions. As there is a line of evidence that the spins of Fe in M(B) would take an ordered state at extremely low temperatures, ilvaite magnetism may be regarded as basically antiferromagnetic. The magnetic spins of Fe in M(A) and M(B) undergo magnetic transitions at different specific temperatures, thus giving as a whole unusual features of magnetism. 相似文献
18.
Metasomatic oxidation of upper mantle periodotite 总被引：1，自引：0，他引：1
Anne V. McGuire M. Darby Dyar Jane E. Nielson 《Contributions to Mineralogy and Petrology》1991,109(2):252-264
Examination of Fe3+ in metasomatized spinel peridotite xenoliths reveals new information about metasomatic redox processes. Composite xenoliths from Dish Hill, California possess remnants of magmatic dikes which were the sources of the silicate fluids responsible for metasomatism of the peridotite part of the same xenoliths. Mössbauer spectra of mineral separates taken at several distances from the dike remnants provide data on Fe3+ contents of minerals in the metasomatized peridotite. Clinopyroxenes contain 33% of total iron (FeT) as Fe3+ (Fe3+/FeT=0.33); orthopyroxenes contain 0.06–0.09 Fe3+/FeT; spinels contain 0.30–0.40 Fe3+/FeT; olivines contain 0.01–0.06 Fe3+/FeT; and metasomatic amphibole in the peridotite contains 0.85–0.90 Fe3+/FeT. In each mineral, Fe3+ and Fe2+ cations per formula unit (p.f.u.) decrease with distance from the dike, but the Fe3+/FeT ratios of each mineral do not vary. Clinopyroxene, spinel, and olivine Fe3+/FeT ratios are significantly higher than in unmetasomatized spinel peridotites. Metasomatic changes in Fe3+/FeT ratios in each mineral are controlled by the oxygen fugacity of the system, but the mechanism by which each phase accommodates this ratio is affected by crystal chemistry, kinetics, rock mode, fluid composition, fluid/rock ratio, and fluid-mineral partition coefficients. Ratio increases in pyroxene and spinel occur by exchange reactions involving diffusion of Fe3+ into existing mineral grains rather than by oxidation of existing Fe2+ in peridotite mineral grains. The very high Fe3+/FeT ratio in the metasomatic amphibole may be a function of the high Fe3+/FeT of the metasomatic fluid, crystal chemical limitations on the amount of Fe3+ that could be accommodated by the pyroxene, spinel, and olivine of the peridotite, and the ability of the amphibole structure to accommodate large amounts of 3 + valence cations. In the samples studied, metasomatic amphibole accounts for half of the bulk-rock Fe2O3. This suggests that patent metasomatism may produce a greater change in the redox state of mantle peridotite than cryptic metasomatism. Comparison of the metasomatized samples with unmetasomatized peridotites reveals that both Fe2+ and Fe3+ cations p.f.u. were increased during metasomatism and 50% or more of iron added was Fe3+. With increasing distance from the dike, the ratio of added Fe3+ to added Fe2+ increases. The high Fe3+/FeT of amphibole and phlogopite in the dikes and in the peridotite, and the high ratios of added Fe3+/added Fe2+ in pyroxenes and spinel suggest that the Fe3+/FeT ratio of the metasomatic silicate fluid was high. As the fluid perolated through and reacted with the peridotite, Fe3+ and C–O–H volatile species were concentrated in the fluid, increasing the fluid Fe3+/FeT. 相似文献
19.
Red Fe3+-rich and black Fe3+, Fe2+-rich tourmalines have been studied by optical and Mössbauer spectroscopies to determine the optical characteristics of Fe3+ in tourmaline. Prominent optical absorption features at 485 and 540 nm are assigned to transitions of multiple exchange-coupled Fe3+ pairs in several site combinations. These transitions are more intense than those of isolated Fe3+ and are polarized along the vector between the interacting ions, thus permitting site assignments. The 485 nm band occurs at an unusually low energy for Fe3+ in silicate minerals. Similar behavior has been observed in the spectrum of coalingite, Mg10Fe 2 3+ (OH)24CO3·2H2O, in which Fe3+ occurs in related pairs in edge-shared sheets. These lower energies are proposed to result from magnetic exchange in edge-shared geometries. Antiferromagnetic exchange has been confirmed by a variable temperature magnetic susceptibility study of a Kenyan dravite with 3.36 wt percent Fe. The Mössbauer spectrum of this sample is unusual in that it shows a pronounced decrease in width of component peaks from 298 K to 5 K. 相似文献
20.
《Applied Geochemistry》2001,16(9-10):1201-1213
In a core of sub-aquatic sediment from Erhai Lake, southwestern China, 4 Fe species were identified as paramagnetic Fe3+, superparamagnetic Fe3+, hematite Fe3+, and paramagnetic high-spin Fe2+ using Mössbauer spectroscopy. The 120 cm core has a distinct lithological boundary at a depth of about 70 cm. Each Fe species has a distinctive distribution with depth. These results represent the redox conditions within the sediment, and also probably reflect the primary sedimentary environments. With increasing burial depth, hematite (Fe2O3) decreased, especially below depths greater than 25 cm, and finally disappeared at around 95 cm. The summed paramagnetic Fe3+ (superparamagnetic Fe3++paramagnetic Fe3+) did not change as much, only exhibiting a slight decrease at depths greater than 75 cm, about 5 cm beneath the lithological boundary within the core. The intensity of paramagnetic high-spin Fe2+ increased with depth. These vertical variations were in harmony with organic geochemical parameters such as TOC concentration, H-index and O-index, indicating that reducing conditions are strongly intensified in the sediment below 70 cm. The geological, organic geochemical and 14C data combined with the present Mössbauer spectroscopic study give a strong indication that the redox environment of Erhai Lake probably shifted rather rapidly from a deep reducing to a shallow oxic state at about 2 ka ago. 相似文献