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1.
Micro-X-ray absorption near-edge structure (XANES) analysis was employed to determine the content of ferric iron in minerals formed in ultrahigh-pressure (UHP) eclogites. It is observed that omphacite and phengite contain significant amounts of Fe3+/Fetot (0.2–0.6), whereas only very low contents are present in garnet (Fe3+/Fetot=0.0–0.03), the latter being consistent with results from stoichiometric charge-balance calculations. Furthermore, considerable variations in the Fe3+/Fetot ratios of omphacite and phengite are observed depending on the textural sites and local bulk chemistry (eclogite and calc-silicate matrix) within one thin section. The oxidation state of isofacial minerals is thus likely to depend on the local fluid composition, which, in the studied case, is controlled by calcareous and meta-basic mineral compositions. These first in-situ measurements of ferric iron in an eclogite sample from the Dabie Shan, E China, are used to recalculate geothermobarometric data. Calculations demonstrate that the temperature during UHP metamorphism was as high as 780 °C, about 80–100 °C higher than previously estimated. Temperatures based on charge balance calculations often give erroneous results. Pressure estimates are in good agreement with former results and confirm metamorphism in the stability field of diamond (43.7 kbar at 750 °C). These P–T data result in a geothermal gradient of ca. 6 °C/km during UHP metamorphism in the Dabie Shan. However, accounting for ferric iron contents in geothermobarometry creates new difficulties inasmuch as calibrations of geothermometers may not be correctable for Fe3+ and the actual effect on Mg–Fe2+ partitioning is unknown. The present study further shows that micro-XANES is a promising technique for the in situ determination of ferric iron contents without destroying the textural context of the sample: a clear advantage compared to bulk methods.  相似文献   

2.
Anders Lindh 《Lithos》1972,5(4):325-343
Phase relations in the system FeO---Fe2O3---TiO2, at temperatures ranging between 300°C and 700°C, have been investigated experimentally with special refference to the reaction Fe3O4 + TiO2 = Fe2O3 + FeTiO3. Pressure was varied between 500 and 2000 bars but its effect was negligible. Magnetite and rutile are the stable assemblage at temperatures above 550 dgC, and hematite and ilmenite are stable for lower temperatures. The equilibrium oxygen fugacity is estimated to be 10−17.5 bars at equilibrium temperature. It is suggested that intermediate hematite-ilmenite solid solutions are inhomogeneous, consisting of ‘domains’ of hematite and ilmenite. The ‘domains’ are too small to be resolved by X-ray diffraction techniques. The top of the solvus curve in the hematite-ilmenite solution corresponds to a temperature of 660°C. Regular solution theory is not applicable to the solid solution.  相似文献   

3.
青海省东昆仑造山带洪水河铁矿床为一中型铁矿床,其含铁建造产于狼牙山组千枚岩中,矿石类型主要为块状磁铁石英岩型,少量为条带状磁铁石英岩型,前人一般认为其属于沉积变质型铁矿床。本文在前人研究基础上,对洪水河铁矿区含铁建造中块状铁矿石进行了铁同位素、主量元素、稀土元素和微量元素分析。结果显示：除1件样品外,其余含铁建造样品的铁同位素δ56FeIRMM014均介于0.97‰~1.97‰之间,和全球典型新元古代含铁建造的Fe同位素特征基本一致;铁矿石的SiO2+Fe2O3质量分数高达78.56%~98.06%,具有极低的Al/(Al+Fe+Mn)值（0.00~0.06）,为典型的化学沉积岩;总稀土元素（w (∑REE)）变化范围为(16.49~80.89)×10-6,没有明显的Ce异常(Ce/Ce*为0.93~1.05),轻稀土元素轻微亏损,显示出类似新元古代含铁建造型的特点。综合对比洪水河铁矿区含铁建造的Fe同位素组成、沉积时代和地球化学特征,推断洪水河铁矿区含铁建造的沉积环境为新元古代柴达木—东昆北陆块的被动大陆边缘构造环境,铁等成矿物质主要来源于海相热液流体;富含Fe2+的海相热液流体上涌并逐渐演变为低温热液后在亚氧化水体环境中与含氧海水混合,最后导致Fe2+被部分氧化并形成氢氧化铁,氢氧化铁逐渐沉积在大陆斜坡上最终形成含铁建造。洪水河铁矿的成因类型可划归为拉皮坦型新元古代含铁建造。  相似文献   

4.
Stephan Klemme   《Lithos》2004,77(1-4):639-646
The position of the transition from spinel peridotite to garnet peridotite in a simplified chemical composition has been determined experimentally at high pressures and high temperatures. The univariant reaction MgCr2O4+2Mg2Si2O6=Mg3Cr2Si3O12+Mg2SiO4, has a negative slope in P–T space between 1200 °C and 1600 °C. The experimental results, combined with assessed thermodynamic data for MgCr2O4, MgSiO3 and Mg2SiO4 give the entropy and enthalpy of formation of knorringite garnet (Mg3Cr2Si3O12). Thermodynamic calculations in simplified chemical compositions indicate that Cr shifts the garnet-in reaction to much higher pressures than previously anticipated. Moreover, in Cr-bearing systems a pressure–temperature field exists where garnet and spinel coexist. The width of this divariant field strongly depends on the Cr/(Cr+Al) of the system.  相似文献   

5.
Takashi Nakajima 《Lithos》1982,15(4):267-280
Sanbagawa metabasites metamorphosed at conditions near the upper limit of the pumpellytic-actinolite facies were examined in terms of phase equilibria in the five component system Al2O3---Fe2O3---CaO---MgO---FeO. The Fe3+ content of epidote measured as XEpFe (=Fe/(Fe + Al) of epidote) in the assemblage epidote-chlorite-actinolite-pumpellyite decreases gradually towards the higher-grade, pumpellyite-free areas. The progressive change in XFeEp can be detected within one metabasite bed 200 meters thick near the upper limit of the pumpellyite-actinolite facies. The Mg---Fe2+ substitution, as expressed by variation of Fe/(Fe + Mg) in chlorite (0.40–0.55) has little effect on the Fe3+ + Al) ratios of epidote and pumpellyite in the above-mentioned assemblage. The lowet XFeEp in the pumpellite-bearing assemblage is 0.15 and hence the upper limit of the pumpellyite-actinolite facies is defined by the appearance of an epidote-chlorite-actinolite assemblage with XEpFc = C.15  相似文献   

6.
The quantitative determination of the main compounds Al (OH)3 (gibbsite) as Al2O3 and hydrated Fe-oxides as Fe2O3 in natural and beneficiated ferruginous bauxites (low-grade bauxites) by X-ray diffraction (XRD) is presented employing the external standard method. The calibration parameters for the analysis by XRD were ascertained by using ten synthetic mixtures of the pure oxides Al2O3 and Fe2O3 which were calcined at 1200°C. The concentration ranges for Fe2O3 were 10–70 wt.% and those for alumina 30–90 wt.%. The standard deviation for the calibrations of the two oxides was 3.33 wt.%. The results obtained by XRD for both oxides were compared with those attained by X-ray fluorescence. The precision of the determinations by XRD was ascertained by analysing a natural sample consecutively 5 times. The accuracy was verified by the analysis of two international standard reference materials with low silica contents.  相似文献   

7.
郭文琳  苏文博 《现代地质》2014,28(2):243-255
最近在河北涞水紫石口剖面的中元古界铁岭组-下马岭组界线(~1400 Ma)附近,发现了一套保存完好的碳酸盐岩古风化壳。野外观测和岩石矿物学研究显示,该古风化壳的岩性以含褐铁矿的铁质泥岩和伊利石粘土岩为主。相对上地壳平均化学组分来说,古风化壳的主量元素氧化物中Al2O3、TiO2、Fe2O3和K2O富集,SiO2轻微亏损,CaO、MgO和Na2O强烈亏损;微量元素中Sc、Cu、Ga、Zr、Hf、Nb、Ta、In、Th、Li、V、Zn、Rb、Cs、W、Pb、U、Mo和Bi等化学性质稳定或易吸附于粘土中的元素含量接近上地壳平均化学组分值或呈不同程度富集,易溶元素Cr、Sr和Cd相对亏损;稀土元素全部富集,轻稀土元素与重稀土元素分异程度大,Ce正异常,Eu负异常。U/Th、Fe3+/Fe2+、Ce的正异常、化学蚀变指数与风化淋滤指数等多种指标都指示该古风化壳是在强氧化的中等到强烈的风化淋滤程度条件下形成。上述研究表明,在中元古代盖层纪(Calymmian Period,1600~1400 Ma)与延展纪(Ectasian Period,1400~1200 Ma)之交,剖面所在的华北克拉通北部应属于温暖湿润的热带-亚热带气候。  相似文献   

8.
A series of granitoids from Proterozoic to Cenozoic age occurred in the western Kunlun orogenic belt, Xinjiang, northwestern China. Several intrusions such as the West Datong (Middle Caledonian age), North Kuda (Late Caledonian age) and Kuzigan, Karibasheng, Zankan (Himalayan age) plutons have shoshonitic affinity. Their rock assemblages include (quartz) monzodiorite–(quartz) monzonite–quartz syenite (Middle Caledonian) or monzonitic granite–granite (Late Caledonian) or biotite (monzonitic) granite–diopside granite–diopside syenite (Himalayan). Generally, biotite is iron–phlogopite, with some eastonite and high Mg/(Mg+FeT) and Fe3+/Fe2+ ratio. Amphibole is mainly edenitic hornblende and magnesian hastingsitic hornblende, with some edenite and higher Mg/(Mg+FeT) and Fe3+/Fe2+ ratio. The rocks show SiO2 contents of 52.77–71.85% and high K2O+Na2O (mostly >8%, average 9.14%), K2O/Na2O (mostly >1, average 1.50) and Fe2O3/FeO (0.85–1.51, average 1.01) and low TiO2 contents (0.15–1.12%, average 0.57%). Al2O3 contents (13.01–19.20%) are high but variable. The granitoids are prominently enriched in LILE, LREE and volatiles such as F. However, the studied shoshonitic granitoids among the three intrusive periods also show differences in isotopic compositions and trace element concentrations, suggesting their different geneses: the origin of the West Datong pluton is probably related to the involvement of subducted oceanic crust sediments into the mantle source; the North Kuda and Himalayan plutons could have been generated by partial melting of subducted oceanic crust sediments or metasediments of thickened continental lower crust in the process of late-orogenic slab break-off or lithospheric thinning.  相似文献   

9.
The effect of Fe-oxidizing bacteria on Fe-silicate mineral dissolution   总被引：11，自引：0，他引：11  
Acidithiobacillus ferrooxidans are commonly present in acid mine drainage (AMD). A. ferrooxidans derive metabolic energy from oxidation of Fe2+ present in natural acid solutions and also may be able to utilize Fe2+ released by dissolution of silicate minerals during acid neutralization reactions. Natural and synthetic fayalites were reacted in solutions with initial pH values of 2.0, 3.0 and 4.0 in the presence of A. ferrooxidans and in abiotic solutions in order to determine whether these chemolithotrophic bacteria can be sustained by acid-promoted fayalite dissolution and to measure the impact of their metabolism on acid neutralization rates. The production of almost the maximum Fe3+ from the available Fe in solution in microbial experiments (compared to no production of Fe3+ in abiotic controls) confirms A. ferrooxidans metabolism. Furthermore, cell division was detected and the total cell numbers increased over the duration of experiments. Thus, over the pH range 2–4, fayalite dissolution can sustain growth of A. ferrooxidans. However, ferric iron released by A. ferrooxidans metabolism dramatically inhibited dissolution rates by 50–98% compared to the abiotic controls.

Two sets of abiotic experiments were conducted to determine why microbial iron oxidation suppressed fayalite dissolution. Firstly, fayalite was dissolved at pH 2 in fully oxygenated and anoxic solutions. No significant difference was observed between rates in these experiments, as expected, due to extremely slow inorganic ferrous iron oxidation rates at pH 2. Experiments were also carried out to determine the effects of the concentrations of Fe2+, Mg2+ and Fe3+ on fayalite dissolution. Neither Fe2+ nor Mg2+ had an effect on the dissolution reaction. However, Fe3+, in the solution, inhibited both silica and iron release in the control, very similar to the biologically mediated fayalite dissolution reaction. Because ferric iron produced in microbial experiments was partitioned into nanocrystalline goethite (with very low Si) that was loosely associated with fayalite surfaces or coated the A. ferrooxidans cells, the decreased rates of accumulation of Fe and Si in solution cannot be attributed to diffusion inhibition by goethite or to precipitation of Fe–Si-rich minerals. The magnitude of the effect of Fe3+ addition (or enzymatic iron oxidation) on fayalite dissolution rates, especially at low extents of fayalite reaction, is most consistent with suppression of dissolution by interaction between Fe3+ and surface sites. These results suggest that microorganisms can significantly reduce the rate at which silicate hydrolysis reactions can neutralize acidic solutions in the environment.  相似文献   


10.
Cordierite samples from pegmatites and metamorphic rocks have been analysed for major [electron microprobe analysis (EMPA)] and trace elements [inductively coupled plasma mass spectrometry (ICP-MS), secondary ion mass spectrometry analyses (SIMS)] as well as for H2O and CO2 (coulometric titration), and the results evaluated in conjunction with published data in order to determine which exchange mechanisms are significant. Apart from the homovalent substitutions FeMg−1 and MnMg−1 on the octahedral site, some minor KNa−1 on the Ch0 channel site, and Fe3+Al−1 on the T11 tetrahedral site, the three most important substitution mechanisms are those for the incorporation of Li on the octahedral sites (NaLi□−1Mg−1), and of Be and other divalent cations on the tetrahedral T11 site (NaBe□−1Al−1 and Na(Mg,Fe2+)□−1Al−1). The dominant role of the last vector is clearly demonstrated. We propose a new generalized formula for cordierite: Ch(Na,K)0–1 VI(Mg,Fe2+,Mn,Li)2 IVSi5 IVAl3 IV(Al, Be, Mg, Fe2+, Fe3+)O18 *xCh(H2O, CO2…). Our results show that the population of (Mg, Fe2+) on the T11-site is limited to about 0.08 a.p.f.u. Other exchange mechanisms that were encountered in experiments operate only under P–T conditions or in bulk compositions that are rarely realized in nature. Routine analyses by electron microprobe in which Li and Be are not determined can be plotted as (Mg+Fe+Mn) versus (Si+Al) to assess whether significant amounts of Li and Be could be present. These amounts can be calculated as Li (a.p.f.u.)=Al+Na–4 and Be (a.p.f.u.)=10–2Al–M2+–Na.  相似文献   

11.
Dag Eigil Ormaasen 《Lithos》1977,10(4):291-310
The Hopen massif, intrusive age 1900 m.y., exposed area 15 km2, in the Lofoten-Vesterålen granulite facies province has the mineral assemblages: (1) mesoperthite+plagioclase (An7–20)+quartz+clinopyroxene (Di20–25)+orthopyroxene En15–25+opaques±minor amphibole±minor biotite; (2) mesoperthite+plagioclase (An <2)+quartz+clinopyroxene (Di <10)+olivine Fe lt;5)+opaques. By using mineral and whole rock analyses, the crystallization conditions were estimated to be 1000°C, 12 kb load pressure and an oxygen fugacity approximately corresponding to the WM buffer. Rocks with the assemblage of type (2) contain secondary orthoferrosilite (Fe0.90–0.95Mn0.04–0.07Mg0.01Ca0.01)2Si2O6, generated by reactions involving fayalite, magnetite and quartz at 800°C, 10kb load pressure and at oxygen fugacities approaching QFM buffer conditions. Subsequent to a crustal thickening, the mangeritic rocks in Lofoten-Vesterålen were emplaced in a tensional environment comparable with modern continental rifts. A ‘gabbro pillow’ magma chamber at the crustal base is proposed as parental magma for the mangeritic rocks, of which the Hopen massif represents a late differentiation.  相似文献   

12.
The exchange of Fe2+ and Mg2+ between orthopyroxene and sapphirine has been investigated at pressures 7-16 kbar and temperatures 850-1300°C using a piston cylinder apparatus for the synthetic and natural systems. This reaction is temperature-dependent and would be a good geothermometer. The equilibration temperature T is approximately expressed by the distribution coefficient as follows: T(°C)=1515/(ln KD+0.943)-273.

This empirical equation was applied to some Antarctic granulites and associated rocks. The new orthopyroxene-sapphirine geothermometer gives consistent results with those estimated from the Fe-Mg orthopyroxene-garnet geothermometer.  相似文献   


13.
T. Agata 《Lithos》1994,33(4):241-263
The Asama igneous complex comprises layered mafic and ultramafic plutonic rocks exposed over about 500×6000 m in the Mikabu greenstone belt, Sambagawa metamorphic terrain of Mie Prefecture; its margins terminate by faults, and there is no trace of chilled rocks. The exposed layered sequence is about 460 m thick, and includes dunite, plagioclase wehrlite, olivine gabbro and two-pyroxene gabbro. The crystallization sequence of essential cumulus minerals is olivine, followed by plagioclase and clinopyroxene together, and finally the appearance of orthopyroxene. Olivine systematically varies in composition from Fo89 to Fo78 with stratigraphic height in the lower to middle portion of the layered sequence. The composition of clinopyroxene changes from Ca49Mg46Fe5 to Ca40Mg47Fe13 upward in the layered sequence; cumulus orthopyroxene, which occurs at the top of the exposed layered sequence, has a composition of Ca2Mg74Fe24. Cumulus chromite occurs as disseminated grains in peridotitic rocks, and tends to increase its Fe3+/(Cr+Al+Fe3+) ratio with stratigraphic height. The most aluminous chromite [Cr/(Cr+Al) = 0.48] occurs in dunite that crystallized shortly before plagioclase began to separate as an essential phase. The Cr/(Cr+Al) ratio of the most aluminous chromite, coupled with the crystallization order of essential minerals, suggests that the Asama parental magma was moderately enriched in plagioclase and clinopyroxene components in the normative mineral diagram plagioclase-clinopyroxene-orthopyroxene. It was similar to a Hawaiian tholeiite and different from the Bushveld and Great “Dyke” parental magmas that were more enriched in orthopyroxene component; it also differed from mid-oceanic ridge basalts that are more depleted in the orthopyroxene component. The Asama clinopyroxene and chromite show characteristically high TiO2 contents and are also similar to those in Hawaiian tholeiites. The Asama igneous complex probably resulted from the crystallization of a magma of a Hawaiian (oceanic-island) tholeiite composition and formed in an oceanic island regime.  相似文献   

14.
We report here for the first time, the occurrence of sapphirine+quartz assemblage in textural equilibrium from quartzo-feldspathic and pelitic granulites from southern India. The sapphirine-bearing rocks occur as layered gneisses associated with pink granite within massive charnockite in Rajapalaiyam area in the southern part of Madurai Block. Sapphirine occurs in three associations: (i) fine-grained subhedral mineral associated with quartz enclosed in garnet, (ii) intergrowth with Al-rich orthopyroxene (up to 9.7 wt.% Al2O3), and (iii) in symplectitic intergrowth with orthopyroxene (Al2O3= 5.9–6.7 wt.%) and cordierite surrounding garnet. The sapphirine in association with quartz is slightly magnesian (XMg = 0.79–0.80) and low in Si content (1.55–1.56 pfu) as compared with those associated with orthopyroxene and cordierite (XMg= 0.77–0.79, Si = 1.59–1.63 pfu). The sapphirine+quartz assemblage suggests that the granulites underwent T>1050 °C peak metamorphism. Cores of porphyroblastic orthopyroxene in the sapphirine-bearing rocks shows high-Al2O3 content of up to 9.7 wt.%, suggesting T = 1040–1060°C and P = 8 kbar. FMAS reaction of sapphirine+quartz→garnet+sillimanite+cordierite indicates a cooling from sapphirine+quartz stability field after the peak ultrahigh-temperature metamorphism. Slightly lower temperature estimates from ternary feldspar and sapphirine-spinel geothermometers (T = 950–1000°C) also support a post-peak isobaric cooling. Corona textures of orthopyroxene+cordierite (±sapphirine), orthopyroxene+sapphirine, and cordierite+spinel around garnet suggest subsequent decompression. The sapphirine-quartz association and related textures reported in this study have important bearing on the ultrahigh-temperature metamorphism and exhumation history of the Madurai Block as well as on the tectonic evolution of the continental deep crust in southern India.  相似文献   

15.
杨松林 《古地理学报》2020,22(2):321-332
钱家店砂岩型铀矿床是松辽盆地发现的特大型铀矿床,目前已发现的铀矿主要赋存在上白垩统姚家组下段,矿体呈板状、透镜状,主要受层间氧化带控制。通过对钱家店砂岩型铀矿层间氧化带各带(氧化带、过渡带及还原带)的主量元素、微量元素、稀土元素进行测试分析,结果表明各带地球化学特征存在较大的差异,其中依据Fe2O3、FeO、Al2O3、SiO2、Na2O及K2O可对层间氧化带进行较准确的分带,MgO、CaO具有一定的分带指示意义。从氧化带到过渡带,趋于富集的微量元素主要为放射性元素(U)、大离子亲石元素(Li、Ba)、亲硫元素(Ni)、高场强元素(Nb、Ta)和性质活跃的变价元素(Mo)等,且 LREE、MREE和HREE均有不同程度富集,反映了水—岩作用时间较长、强度较大。有机碳、S全、ωFe3+/ωFe2+还原性指标在不同分带的显著差异表明,随着含氧含铀水在姚家组地层中迁移,还原性组分变化强烈,具有明显的分带指示意义。  相似文献   

16.
Marcasite precipitation from hydrothermal solutions   总被引：3，自引：0，他引：3  
Pyrite and marcasite were precipitated by both slow addition of aqueous Fe2+ and SiO32− to an H2S solution and by mixing aqueous Fe2+ and Na2S4 solutions at 75°C. H2S2 or HS2− and H2S4 or HS4− were formed in the S2O32− and Na2S4 experiments, respectively. Marcasite formed at pH < pK1 of the polysulfide species present (for H2S2, pK1 = 5.0; for H2S4, pK1 = 3.8 at 25°C). Marcasite forms when the neutral sulfane is the dominant polysulfide, whereas pyrite forms when mono-or divalent polysulfides are dominant. In natural solutions where H2S2 and HS2 are likely to be the dominant polysulfides, marcasite will form only below pH 5 at all temperatures.

The pH-dependent precipitation of pyrite and marcasite may be caused by electrostatic interactions between polysulfide species and pyrite or marcasite growth surfaces: the protonated ends of H2S2 and HS2 are repelled from pyrite growth sites but not from marcasite growth sites. The negative ions HS2 and S22− are strongly attracted to the positive pyrite growth sites. Masking of 1πg* electrons in the S2 group by the protons makes HS2 and H2S2 isoelectronic with AsS2− and As22−, respectively ( et al., 1981). Thus, the loellingitederivative structure (marcasite) results when both ends of the polysulfide are protonated.

Marcasite occurs abundantly only for conditions below pH 5 and where H2S2 was formed near the site of deposition by either partial oxidation of aqueous H2S by O2 or by the reaction of higher oxidation state sulfur species that are reactive with H2S at the conditions of formation e.g., S2O32− but not SO42−. The temperature of formation of natural marcasite may be as high as 240°C ( and , 1985), but preservation on a multimillion-year scale seems to require post-depositional temperatures of below about 160°C ( , 1973; and , 1985).  相似文献   


17.
The redox state of subduction zones: insights from arc-peridotites   总被引：23，自引：0，他引：23  
Spinel peridotites from a variety of island arcs have been utilised to calculate the redox state of the mantle wedge above subduction zones. Oxygen fugacities (fO2 values) calculated from the ferric iron content of spinels, measured by Electron Microprobe (EMP) using secondary standards [Wood, B.J., Virgo, D., 1989. Upper mantle oxidation state: ferric iron contents of lherzolite spinels by 57Fe Mössbauer spectroscopy and resultant oxygen fugacities. Geochim. Cosmochim. Acta, 53, 1277–1291.], yield values which range from 0.3 to 2.0 above the fayalite–magnetite–quartz (FMQ) buffer. These data provide further evidence that the mantle wedge is ubiquitously oxidised relative to oceanic and ancient cratonic mantle. There is no correlation between fO2 values and the presence of hydrous phases and, in fact, the most oxidised samples contain no hydrous phases. Within individual suites there is no correlation between fO2 and degree of depletion as indicated by spinel Cr#, except for a suite of reacted forearc-peridotites. However, when the data is viewed as a whole there is broad a positive correlation between fO2 and spinel Cr# suggesting that partial melting processes may influence the redox state of the mantle wedge. We suggest that the ultimate source of the oxygen which oxidises the mantle wedge is from the subducted slab. It is not clear whether this oxidising agent is a solute-rich hydrous fluid or a water-bearing silicate melt. However, our data does indicate that silicate melts are effective oxidisers of the depleted shallow upper mantle. Simple mass balance calculations based on the ferric iron content of primitive subduction zone magmas indicates that the source region must contain 0.6–1.0 wt.% Fe2O3. This amount of Fe2O3 in a fertile spinel peridotite yields an oxygen fugacity of 0.5–1.7 log units above FMQ in the IAB source. If water is the sole oxidising agent in the mantle wedge then 0.030–0.075 wt.% H2O is required which is considerably less than the 0.25% H2O envisaged by Stolper and Newman [Stolper, E.M., Newman, S., 1994. The role of water in the petrogenesis of Mariana trough magmas. Earth Planet. Sci. Lett., 121, 293–325.], suggesting water is not necessarily an efficient oxidising agent. Alternatively, ferric iron may be added to the mantle wedge by addition of a ferric iron-rich sediment melt or more likely as a solute-rich hydrous fluid. This model would produce spinel, orthopyroxene or amphibole in the wedge with only a slight increase in fO2 of the source region. Although it is unclear which model is correct the maximum fO2 of the fertile mantle wedge is unlikely to be above FMQ+2 and therefore some decompression melting in the mantle wedge is required to explain the higher fO2 values of primitive arc lavas than arc-peridotites.  相似文献   

18.
The Qianjiadian sandstone-type uranium deposits is a large uranium deposits discovered in the Songliao Basin. The uranium deposits discovered mainly occur in the Lower Member of the Upper Cretaceous Yaojia Formation. The ore body is tabular and lenticular,mainly controlled by the interlayer oxidation zone. By testing and analyzing the main elements,trace elements and rare earth elements in the oxidation zone of the Qianjiadian sandstone-type uranium deposits(oxidation zone,transition zone and reduction zone),the results show that the geochemical characteristics of each zone vary greatly,where the interlayer oxidation zone can be zoned relatively accurately by Fe2O3,FeO,Al2O3,SiO2,Na2O and K2O and MgO and CaO have certain indication significance for zoning. From the oxidation zone to the transition zone,the trace elements that tend to be enriched are mainly radioactive elements(U),large ion lithophile elements(Li,Ba),chalcophile elements(Ni),high field strength elements(Nb,Ta),active variable valence elements(Mo),etc.,and LREE,MREE and HREE have different degrees of enrichment,reflecting the long water-rock interaction with large intensity. The significant difference of reducing indexes of organic carbon,St,and ωFe3+/ωFe2+ in different zones indicates that with the migration of oxygen-uranium containing water in the Yaojia Formation,the reducing components change sharply and have obvious significance of zoning indication.  相似文献   

19.
Status report on stability of K-rich phases at mantle conditions   总被引：1，自引：0，他引：1  
George E. Harlow  Rondi Davies 《Lithos》2004,77(1-4):647-653
Experimental research on K-rich phases and observations from diamond inclusions, UHP metamorphic rocks, and xenoliths provide insights about the hosts for potassium at mantle conditions. K-rich clinopyroxene (Kcpx–KM3+Si2O6) can be an important component in clinopyroxenes at P>4 GPa, dependent upon coexisting K-bearing phases (solid or liquid) but not, apparently, upon temperature. Maximum Kcpx content can reach 25 mol%, with 17 mol% the highest reported in nature. Partitioning (K)D(cpx/liquid) above 7 GPa=0.1–0.2 require ultrapotassic liquids to form highly potassic cpx or critical solid reactions, e.g., between Kspar and Di. Phlogopite can be stable to about 8 GPa at 1250 °C where either amphibole or liquid forms. When fluorine is present, it generally increases in Phl upon increasing P (and probably T) to about 6 GPa, but reactions forming amphibole and/or KMgF3 limit F content between 6 and 8 GPa. The perovskite KMgF3 is stable up to 10 GPa and 1400 °C as subsolidus breakdown products of phlogopite upon increasing P. (M4)K-substituted potassic richterite (ideally K(KCa)Mg5Si8O22(OH,F)2) is produced in K-rich peridotites above 6 GPa and in Di+Phl from 6 to 13 GPa. K content of amphibole is positively correlated with P; Al and F content decrease with P. In the system 1Kspar+1H2O K-cymrite (hydrous hexasanidine–KAlSi3O8·nH2O–Kcym) is stable from 2.5 GPa at 400 to 1200 °C and 9 GPa; Kcym can be a supersolidus phase. Formation of Kcym is sensitive to water content, not forming within experiments with H2O2O>Kspar. Phase X, a potassium di-magnesium acid disilicate ((K1−x−n)2(Mg1−nMn3+)2Si2O7H2x), forms in mafic compositions at T=1150–1400 °C and P=9–17 GPa and is a potential host for K and H2O at mantle conditions with a low-T geotherm or in subducting slabs. The composition of phase-X is not fixed but actually represents a solid solution in the stoichiometries □2Mg2Si2O7H2–(K□)Mg2Si2O7H–K2Mg2Si2O7 (□=vacancy), apparently stable only near the central composition. K-hollandite, KAlSi3O8, is possibly the most important K-rich phase at very high pressure, as it appears to be stable to conditions near the core–mantle boundary, 95 GPa and 2300 °C. Other K-rich phases are considered.  相似文献   

20.
断裂构造中元素的迁移变化规律是构造地球化学研究的主要内容.白山市板石沟铁矿断裂构造发育,是开展断裂构造地球化学研究的有利地区.通过对板石沟铁矿17矿组和赵家沟矿组典型逆断层剖面测量,采集构造岩和周围岩石,分析常量元素和微量元素,利用构造地球化学剖面法、质量等比线法和特征元素比值来反映元素在逆断层中分布特征和迁移变化规律.通过分析认为在逆断层中常量元素SiO2、Fe2O3、CaO、Na2O亏损,Al2O3、K2O富集,微量元素中Rb、Sr等离子半径较大元素富集,离子半径较小元素Co、Cr、Ni亏损,K2O/Na2O、V/Cr、Rb/（Ni+Co）在逆断层中呈现出高值,SiO2/Al2O3、（Fe2O3+CaO+MgO）/Al2O3呈现出低值.依据这些构造地球化学特征可以用来判断断裂构造的存在,为断裂构造地球化学研究和板石沟铁矿勘查提供构造地球化学依据.  相似文献   

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