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Summary Upper amphibolite facies gneisses in the southern Indian Shield show local transformation into veins, clots and patches of orthopyroxene-bearing dry granulites (incipient charnockites). Depending upon the protolith composition, these desiccated zones are classified into ortho- and para-charnockites and have developed within rocks of distinct mineralogy and chemistry at different time intervals through the structurally-controlled influx of carbon dioxide-rich fluids. Our geochemical investigations at five critical quarry sections indicate that the incipient charnockites have undepleted chemistry and very low K/Rb values. In the paracharnockite localities, where granulite formation is characterized by consumption of garnet, biotite and quartz to produce orthopyroxene, loss of Rb and Ba and enrichment of Ti are observed. In contrast, the orthocharnockite localities show marked LILE enrichment with gain of K, Rb and Ba and loss of CaO, suggesting extensive replacement of plagioclase in the gneisses by K-feldspar in the charnockite through K-Na-Ca exchange reactions with influxing carbonic fluids. The marked depletion in Fe, Mg, Ti and P in these rocks correlates with progressive dissolution of hornblende, biotite, magnetite and accessory apatite. Our study indicates that gneiss to granulite transformation, even if on a local scale, is not an isochemical phenomenon, but attended by distinct element mobilities, although they are contrastingly different from the geochemical trends in some regional high grade terrains.
Geochemie von Gneiss-Granulit-Übergängen in den Incipient Charnockite Zonen von Süd-Indien
Zusammenfassung Gneise der oberen Amphibolit-Fazies im Südteil des Indischen Schildes zeigen lokal Umwandlungen in Adern, and unregelmäßigen Bereichen von orthopyroxen-führenden trockenen Granuliten (Incipient Charnockites). In Abhängigkeit von der Zusammensetzung des Ausgangsgesteins werden diese Zonen in Ortho- und Paracharnockite eingeteilt. Sie entwickelten sich in Gesteinen von charakteristischer mineralogischer und chemischer Zusammensetzung zu verschiedenen Zeit-Intervallen durch die tektonisch kontrollierte Zufuhr von kohlendioxid-reichen Fluiden. Unsere geochemischen Untersuchungen an fünf strategisch ausgewählten Steinbruchen zeigen, daß die Incipient Charnockite eine nicht verarmte chemische Zusammensetzung und sehr niedrige K/Rb Werte haben. In den Paracharnockit-Lokalitäten, wo Granulitbildung charakterisiert wird durch das Verschwinden von Granat, Biotit und Quartz, aus denen Orthopyroxene gebildet werden, ist Verlust von Rb und Ba und Anreicherung an Ti zu beobachten. Im Gegensatz dazu zeigen die Orthocharnockite eindeutige LILE Anreicherung mit Zunahme von K, Rb, und Ba und Verlust von Ca0. Dies weist auf extensiven Ersatz von Plagioklas in den Gneisen durch K-Feldspat in den Charnockiten durch K-Na-Ca Austausch-Reaktionen mit zugeführten C02-Fluiden hin. Die deutliche Verarmung an Fe, Mg, Ti und P in diesen Gesteinen wird mit zunehmender Auflösung von Hornblende, Biotit, Magnetit und akzessorischem Apatit erKlärt. Unsere Untersuchungen zeigen, daß die Gneis-Granulit Transformation auch im lokalen Maßstab nicht ein isochemisches Phänomen ist, sondern durch charakteristische Elementtransporte charakterisiert wird. Diese unterscheiden sich jedoch deutlich von den geochemischen Trends, die in einigen regional-metamorphen high grade terrains zu beobachten sind.[/p]相似文献
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X-ray diffraction (XRD), X-ray Fluorescence (XRF), optical microscopy, Scanning Electron Microscopy coupled with Energy Dispersive Spectrometry (SEM-EDS) and Electron Probe micro-analyser (EPMA) and Wavelength-Dispersive Spectroscopy (WDS) were conducted on charnockite from the Caparaó Suite and its alteration cortex to determine the mineralogical, micromorphological and geochemical transformations resulting from the weathering process. The hydrolysis of the charnockite occurred in different stages, in accordance with the order of stability of the minerals with respect to weathering: andesine/orthopyroxene, pargasite and alkali feldspar. The rock modifications had begun with the formation of a layer of incipient alteration due to the percolation of weathering solutions first in the pressure relief fractures and then in cleavage and mineral edges. The iron exuded from ferromagnesian minerals precipitated in the intermineral and intramineral discontinuities. The layer of incipient alteration evolves into an inner cortex where the plagioclase changes into gibbsite by direct alitisation, the ferromagnesian minerals initiate the formation of goethitic boxworks with kaolinitic cores, and the alkali feldspar initiates indirect transformation into gibbsite, forming an intermediate phase of illite and kaolinite. In the outer cortex, mostly traces of alkali feldspar remain, and they are surrounded by goethite and gibbsite as alteromorphics, characterising the formation of the isalteritic horizon that occurs along the slope and explains the bauxitization process at the Caparaó Range, SE Brazil. 相似文献
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M CHANDRA SEKARAN RAJNEESH BHUTANI S BALAKRISHNAN 《Journal of Earth System Science》2016,125(3):605-622
Pudukkottai region in the northeastern part of the Madurai Block exposes the garnetiferous pink granite that intruded the biotite gneiss. Charnockite patches are associated with both the rock types. Rb–Sr biotite and Sm–Nd whole-rock isochron ages indicate a regional uplift and cooling at ～550 Ma. The initial Nd isotope ratios (\(\varepsilon _{\text {Nd}}^{\mathrm {t}}=-20\) to ?22) and Nd depleted-mantle model ages (TDM = 2.25 to 2.79 Ga) indicate a common crustal source for the pink-granite and associated charnockite, while the biotite gneiss and the charnockite within it represent an older crustal source (\(\varepsilon _{\text {Nd}}^{\mathrm {t}}= -29\) and TDM = > 3.2 Ga). The Rb–Sr whole-rock data and initial Sr–Nd isotope ratios also help demonstrate the partial but systematic equilibration of Sr isotope and Rb/Sr ratios during metamorphic mineral-reactions resulting in an ‘apparent whole-rock isochron’. The available geochronological results from the Madurai Block indicate four major periods of magmatism and metamorphism: Neoarchaean–Paleoproterozoic, Mesoproterozoic, mid-Neoproterozoic and late-Neoproterozoic. We suggest that the high-grade and ultrahigh-temperature metamorphism was preceded by magmatism which ‘prepared’ the residual crust to sustain the high P–T conditions. There also appears to be cyclicity in the tectono-magmatic events and an evolutionary model for the Madurai Block should account for the cyclicity in the preserved records. 相似文献
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钇—5—Br—PADAP—CPC—OP显色反应的研究 总被引：6，自引：0，他引：6
研究了钇(Ⅲ)-5-Br-PADAP-CPC-乳化剂OP混合体系的光度特性,在pH7.5～9.8范围内,显色体系在580nm处有最大吸收峰,空白值低,对比度(Δλ)较高,摩尔吸光系数ε为1.0×10~5。配合物组成Y:5-Br-PADAP:CPC为1:4:3,形成稳定常数(logβ)为9.84。在0—45μg Y/50ml范围内服从比尔定律。该法已成功地应用于测定Fe-Cr-Al合金和矿物中痕量钇。 相似文献
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在ＰＨ４．５的ＨＡｃ－ＮａＡｃ介质中,Ｉｎ－１－苯基－３－甲基－４－苯甲酰基吡唑啉酮－５（ＰＭＢＰ）－安替比林体系于－０．５７Ｖ处产生一良好的极谱波。Ｉｎ在０．０１－０．５ｍｇ／Ｌ与波高呈线性关系。 相似文献
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用抽空石英管法研究以Fe_(0·96) Sb_(2·04) S_(4·12)为投影顶点,8×(PbS-SnS-SnS_2)为投影平面的Pb-Sn-Fe-Sb-S体系的相图表明,由于Pb(?)Sn~(2+)之间互相取代,500℃时辉锑锡铅矿固溶体中Sn~(2+)变化范围(以单位分子式11个金属原子总数为计量)是0—4.8个原子,400℃时则为0—4.0个原子。同时,Sn~(4+)变化范围是1.3—2.3个原子和1.5—2.1个原子。圆柱锡矿固溶体变化范围较小。500℃时Sn~(2+)变化范围是0.4—1.8个原子,400℃时为0.5—1.7。Sn~(+4)变化范围则分别为3.2—4.2个原子和3.3—4.2个原子。变更Fe含量(0.81—1.09)及Sb含量(1.83—2.29)进行的几组合成实验表明,上述两个矿物中Fe、Sb含量变化范围很小,不超过±0.15个原子。辉锑锡铅矿固溶体可与方铅矿、块硫锑铅矿、针硫锑铅矿、硫锡铅矿、硫锡矿、圆柱锡矿等形成平衡结线。而圆柱锡矿不与方铅矿、硫锡矿、硫锡铅矿形成平衡结线,但可与辉锑矿、SnS_2及上述其他矿物形成平衡结线。结合锡的硫化物及氧化物(锡石)热力学稳定场计算表明,在本体系内辉锑锡铅矿在300℃时稳定区的硫活度在lga_(s2)=-20(atm)附近,氧活度小于lga_(o2)=-40(atm),而圆柱锡矿稳定区硫活度大于lga_(s2)=-10(atm)。 相似文献
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4—（2—羟基—4—硝基苯偶氮）—1—苯基—3—甲基吡唑啉酮与钍的显色反应 总被引：4，自引：0，他引：4
在pH为 2～ 3的HAc介质中 ,4 - ( 2 -羟基 - 4 -硝基苯偶氮 ) - 1 -苯基 - 3-甲基吡唑啉酮 (HNAPMP)与钍反应生成 2∶1的稳定络合物 ,λmax=540nm ,ε=4 .96× 1 0 4L·moL- 1·cm- 1,Th质量浓度在 0～ 2 .8mg/L内符合比尔定律。方法用于钍钨合金中钍的测定 ,相对标准偏差 (n =5)小于 1 % ,加标回收率为 97%～ 1 0 2 %。 相似文献
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1—（2—羟基—3,5—二硝基苯）—3—4（4—苯基—2—噻唑）—三氮稀的合成及其与镍的显 总被引：7，自引：0，他引：7
合成了新试剂 1 - (2 -羟基 - 3,5-二硝基苯 ) - 3- (4-苯基 - 2 -噻唑 ) -三氮烯 ,研究了在表面活性剂TritonX - 1 0 0存在下 ,它与Ni2 的显色反应。结果表明 ,在 pH 6.0～ 7.5时 ,Ni2 与该试剂形成配合物 ,其最大吸收峰位于 51 5nm处 ,摩尔吸光系数为 1 .0 8× 1 0 5 L·mol- 1 ·cm- 1 。Ni2 在 0～ 0 .4mg/L内符合比尔定律。方法已用于矿物、合金、钢样中微量镍的测定 ,结果与原子吸收法相符 ,相对标准偏差RSD <5% (n =6) 相似文献
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2—[2‘—（6—甲氧基—苯并噻唑）—偶氮]—1,8—二羟基萘—3,6—二磺酸的合成及？… 总被引：2，自引：0，他引：2
合成了新的杂环偶氮变色酸类试剂--2-[2'-(6-甲氧基-苯并噻唑)-偶氮]-1,8-二羟基萘-3,6-二磺酸,并系统探讨了在pH 4.5的邻苯二甲酸氢钾-NaOH介质中显色试剂与钛的显色反应特性.结果表明,在溴化十六烷基吡啶存在下,试剂与Ti(Ⅳ)形成2:1的络合物,显色反应15 min完全并至少稳定4 h,最大吸收波长为670 nm,表观摩尔吸光系数达1.67×105 L.mol-1.cm-1,钛的质量浓度在0～400 μg/L时符合比尔定律.用拟定的方法测定了硅砖等标准物质中的Ti(Ⅳ),所得结果与标准值的相对误差均小于4%,RSD(n=5)小于3.5%. 相似文献
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吴大清 《中国地球化学学报》1990,9(2):155-160
Phase relations in the system Pb-Sn-Fe-Sb-S were investigated through the diagrams of projecting plane 8x(PbS-SnS-SnS2)from the vertrex point Fe0.96Sb2.04S4.12by vacuum silica tube technique.Experimental results have shown that franckeite has a wide solid solution with substitution of Pb^2 by Sn^2 ,In franckeite s.s.the content of Sn^2 varies from 0 to 4.8 atoms (total metal atoms are 11 atoms per formula) at 500℃ and 0-4.0 atoms at 400℃,respectively,Meanwhile,the content of Sn^4 ranges from 1.3to 2.0 atoms at 500℃ and 1.5-2.1 atoms at 400℃ in franckeite s.s.These results are consistent well with analytic data on natural franckeite.The cylindrite solid solutiopn has a relatively small range with Sn^2 -1.8atoms and Sm^4 =3.2-4.2 atoms per formula at 500℃ and ,Sn^2 =0.5-1.7 atoms and Sm^4 =3.3-4.2 atoms at 400℃ which are comparable with natural cylindrite.The phases coexisting in equilibrium with franckeite s.s. are galena,boulangerite,robinsonite.teallite,SnS,cylindrite.s.s.and synthetic phase Ⅲ ss or I ss.The cylindrite s.s.coexists with SnS2 and the above mentioned phases,but not with galena.teallite and SnS,and probably not with boulangerite in this projecting plane. 相似文献
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乙醇与β-环糊精的协同作用,使1,4-二羟基蒽醌-Be体系荧光强度提高10倍以上,反应选择性有所改善。基于此,本文通过实验确定了1,4-二羟基蒽醌-β-环糊精-乙醇荧光体系测定岩石矿物中痕量Be的最佳条件,并就乙醇在其中的作用进行了探讨。 相似文献