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1.
广东天堂矽卡岩型铜铅锌多金属矿床位于钦州—杭州成矿带阳春盆地的东北端边缘。在野外地质观察的基础上,选取该矿床主要金属硫化物开展矿物学特征研究,测定S、Pb同位素组成,探讨其成矿物质来源。电子探针分析发现:黄铁矿中Fe、S含量和S/Fe原子比普遍高于理论值,存在一定量的Cu、Sb、As,Co/Ni比值变化范围为0.21-2.28,一般大于1,指示硫逸度较高的热液环境;闪锌矿中Zn含量比理论值稍低,S/Zn原子比和S含量较理论值偏高,含一定量的Pb、Fe、Co和Se等元素;方铅矿、黄铜矿等硫化物元素间均有类质同象现象的发生。硫化物的δ34S组成范围比较窄,变化范围为-2.1‰-2.6‰,多数集中在-0.8‰-0.4‰,具有明显的塔式分布特征。矿石矿物Pb同位素组成亦比较稳定,208Pb/204Pb、207Pb/204Pb、206Pb/204Pb的变化范围分别为38.765-39.137、15.523-15.751、18.450-18.667,矿石铅既具有下地壳或者上地幔的特征,又具有上地壳的特征,显示混合源特征,表明成矿物质属于壳幔混合型,具有多种物质来源,可能是晚中生代以来华南地区岩石圈伸展作用的产物。 相似文献
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查个勒铅锌钼铜矿床位于念青唐古拉铅锌银铁铜成矿带西段南缘,为查明其成矿物质来源及矿床成因,对该矿床开展了系统的H、O、S、Pb同位素研究,并与念青唐古拉成矿带中-东段典型铅锌(铜钼)矿床进行对比。查个勒矿床石英H、O同位素(δD值介于-189‰～-157‰之间,δ~(18)O_(H_2O)值介于-2.2‰～2.9‰之间)指示其成矿流体主要由岩浆水与大气降水混合组成。矿区北部铅锌矿体硫化物δ~(34)S值为-5.6‰～-0.8‰,均值为-3.7‰,显示岩浆硫和地层硫混合的特征。矿区南部(铜)钼矿体硫化物δ~(34)S值为1.1‰～2.6‰,均值为1.8‰,显示岩浆硫的特征。矿石硫化物和花岗斑岩全岩~(208)Pb/~(204)Pb,~(207)Pb/~(204)Pb,~(206)Pb/~(204)Pb的比值分别为38.988～39.269、39.002～39.559,15.657～15.747、15.643～15.664,18.614～18.688、18.663～19.058。矿石硫化物与花岗斑岩的Pb同位素特征相似,均表现出上地壳Pb源的特征,推测成矿物质主要来自上地壳岩浆源。查个勒矿床H、O、S、Pb同位素特征与中-东段典型铅锌(铜钼)矿床相似,表明念青唐古拉成矿带铅锌(铜钼)矿床成矿流体及成矿物质来源一致。作者认为查个勒矿床是一个受岩浆和构造共同控制的斑岩型(铜)钼+矽卡岩型-热液脉型铜铅锌矿床,在念青唐古拉成矿带,自西向东分布有多处斑岩型(铜)钼矿+矽卡岩型-热液脉型(铜)铅锌矿矿集区。 相似文献
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西藏甲玛铜多金属矿硫同位素地球化学研究 总被引：1，自引：0，他引：1
西藏墨竹工卡县甲玛铜多金属矿床位于冈底斯成矿带东段,Cu、Mo、Pb+Zn、Au、Ag均达大型规模,并伴生Co、Bi、W、Ni等多金属矿化。黄铜矿、斑铜矿、辉钼矿、方铅矿、闪锌矿、黝铜矿、辉铜矿等硫化物为主要的矿石矿物,硫酸盐矿物以硬石膏为主,含矿岩浆岩以花岗斑岩、二长花岗斑岩和花岗闪长斑岩为主。通过对甲玛矿区主要硫化物和硬石膏的硫同位素分析,并结合前人研究,甲玛矿区硫化物的硫同位素δ34S值变化于13.6‰～+12.5‰,平均值1.33‰(样品数86)、硬石膏δ34S值+0.5‰～+1.8‰,平均值+1.13‰(样品数3)、岩浆岩δ34S值0.7‰～0.2‰,平均值0.5‰(样品数3),与岩浆硫δ34S值0±3‰一致。闪锌矿-方铅矿-黄铜矿矿物对的硫同位素地质温度计,显示成矿温度为408～433℃,说明其形成时硫同位素处于平衡状态。冈底斯成矿带上的驱龙等斑岩型矿床中硫化物和岩浆岩硫同位素,均具有δ34S值变化范围小,平均值接近0值,与岩浆硫特征一致的特点,反映了甲玛铜多金属矿床具有矽卡岩-斑岩型矿床硫同位素地球化学特征,硫以岩浆来源为主。 相似文献
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为了示踪德能铜多金属矿床成矿物质来源,本文利用电子探针技术对黄铁矿、黄铜矿、方铅矿和绿泥石进行了矿物化学成分分析,测定了硫化物闪锌矿、方铅矿、黄铁矿的Pb和S同位素组成.结果表明,硫化物中硫含量均低于理论值,其中黄铁矿S/Fe值为1.067~1.094(平均1.083),Co/Ni1,立方体{100}晶形发育,指示其形成于较高温度、较高氧逸度和低硫逸度环境;绿泥石为富铁蠕绿泥石,形成温度为185℃~266℃,反映中低温、酸性、还原条件环境.硫化物铅同位素组成较稳定,208Pb/204Pb比值为38.937~39.217,207Pb/204Pb为15.640~15.718,206Pb/204Pb为18.521~18.601,μ值9.53~9.68,ω值38.29~39.76,指示其铅可能来源于念青唐古拉群基底变质岩;硫化物δ34S值为6.6‰~9.3‰,反映硫可能来自花岗质岩浆. 相似文献
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小土尔根铜矿位于新疆阿尔泰地区诺尔特Au-Pb-Zn(-W-Mo)成矿带北部,成矿条件有利。在详细的野外考察基础上,作者系统分析了矿区的流体包裹体类型、流体成分,结合H-O、Cu同位素地球化学研究,对其成矿流体特征及来源、成矿物质来源和矿床成因进行了探讨。该矿流体包裹体类型比较简单,主要为气液两相包裹体,少量纯液相包裹体,偶见含子晶包裹体。激光拉曼光谱分析表明,成矿流体为H_2O-Na Cl-CO_2-CH_4体系。成矿流体温度介于188~421℃,盐度介于0.71%~15.53%Na Cl_(eqv),主要集中于8.0%~12.0%Na Cl_(eqv),为中?高温、中?低盐度成矿流体。H、O同位素(δD_(SMOW)值介于-72‰~-122‰,δ~(18)O_(fluid)值介于3.7‰~8.1‰)指示,成矿流体主要来源于岩浆水,随着成矿作用的进行,大气降水混入的比例略有增大。黄铜矿的δ~(65)Cu值介于-0.12‰~0.93‰,落入花岗岩δ~(65)Cu值分布范围,且分馏特征与花岗岩相似,说明成矿元素Cu来自花岗岩岩浆。结合前人成果,作者认为小土尔根铜矿应为诺尔特地区首例还原性斑岩铜矿床。 相似文献
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加多捕勒铁铜矿床位于念青唐古拉成矿带西段。综合研究围岩、岩体与矿石的硫、铅同位素组成,发现其矿石硫化物的δ~(34)S值变化范围为-2.1‰～6.2‰,δ~(34)S_(ΣS)值为2.16‰,总体具有岩浆硫的特征。矿石硫化物的δ~(34)S值与石英闪长岩、板岩中硫化物的δ~(34)S值相近,表明矿石的硫源可能部分由板岩与石英闪长岩提供。矿石铅同位素组成比较均一,~(206)Pb/~(204)Pb、~(207)Pb/~(204)Pb和~(208)Pb/~(204)Pb的变化范围分别为18.27～18.842、15.653～15.899和38.793～39.703,与冈底斯成矿带北亚带矿床矿石硫化物的铅同位素组成相近,具有上地壳铅源的特征。矿石铅同位素组成与黑云母二长花岗岩、大理岩的铅同位素组成一致,显示铅可能主要来源于黑云母二长花岗岩和大理岩。综合分析表明,加多捕勒铁铜矿床硫、铅同位素的研究显示其成矿物质可能主要来源于黑云母二长花岗岩,部分来源于中二叠统下拉组岩石,少量由石英闪长岩提供,它们为深入研究该矿床的成矿模式提供了资料。 相似文献
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青海沱沱河地区多才玛铅锌矿床成因:原位S和Pb同位素证据 总被引：2，自引：2，他引：0
青海沱沱河地区多才玛铅锌矿床是西南三江特提斯北段新生代铅锌矿集区的典型矿床之一,本文首次应用飞秒激光剥蚀多接受器等离子体质谱法对多才玛铅锌矿床中金属硫化物的原位S和Pb同位素进行了测定。结果显示:黄铁矿、方铅矿和闪锌矿的原位S同位素的δ~(34)S_(V-CDT)值介于-26.34‰～4.24‰之间,均值-12.15‰(n=20),其中闪锌矿的δ~(34)S_(V-CDT)值介于-10.30‰～-3.52‰,均值-7.39‰(n=9);方铅矿的δ~(34)S_(V-CDT)值为-26.34‰～-11.74‰,均值-20.36‰(n=9);黄铁矿的δ~(34)S_(V-CDT)值分别为2.50‰,4.24‰。矿床δ~(34)S数据范围较宽,总体表现为富集负值硫的特征,说明有机质可能参与成矿。岩浆热液期发育的黄铁矿δ~(34)S值具有深源特征,沉积热液期发育的方铅矿和闪锌矿的δ~(34)S值表明成矿过程存在还原作用,指示盆地地层还原流体的混入,综上可认为多才玛铅锌矿床硫具有混合来源的特征。方铅矿原位Pb同位素结果为~(206)Pb/~(204)Pb=18.866～18.929,~(207)Pb/~(204)Pb=15.674～15.689,~(208)Pb/~(204)Pb=39.052～39.174。方铅矿与地层的Pb同位素组成一致,位于上地壳平均Pb演化线之上,具上地壳和地幔混合俯冲带铅的特征,表明其成矿物质的来源多样。结合矿床学、矿物学及同位素数据,本文认为多才玛铅锌矿床S元素主要来源于赋矿围岩,Pb金属元素主要来源于藏北钾质火山岩,侵入地层岩浆与盆地流体的混合是金属硫化物沉淀的重要机制。 相似文献
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大兴安岭南段多金属成矿带硫、铅同位素组成及其地质意义 总被引：4，自引：0，他引：4
大兴安岭南段是我国北方重要的多金属矿床成矿带,对其成矿物质来源的分析研究有利于区域成矿规律的总结。在前人的工作基础上,对典型矿床的矿石矿物进行了硫、铅同位素研究。结果表明:闪锌矿、方铅矿、毒砂、黄铜矿、辉钼矿等硫化物的δ34S值主要变化范围为-6‰～4‰,平均值为0‰,峰值出现在0‰～2‰,呈塔式分布;无明显的重硫、轻硫富集,说明硫源较单一;矿石矿物及岩石的206 Pb/204 Pb、207Pb/204Pb、208Pb/204Pb值的变化范围主要集中在18.13～18.74、15.38～15.68和37.1～38.93,其平均值分别为18.38、15.54和38.09。同时,数据结果显示:成矿带的东部与西部存在较为明显的铅同位素差异,西部矿床中铅的分布主要集中在造山带演化线附近,而东部矿床中铅主要集中分布在上地幔和造山带演化曲线附近。 相似文献
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德新和轧轧龙铅锌矿是冈底斯西段银铅锌多金属成矿带典型的热液脉型铅锌矿床,关于其成矿物质来源及与纳如松多铅锌矿成因联系的研究鲜有开展。本研究利用单矿物和全岩稳定同位素方法对德新和轧轧龙铅锌矿的主要金属硫化物和含矿花岗斑岩进行了S、Pb同位素组成分析和示踪,结果显示德新铅锌矿硫化物δ34SVCDT为3.5‰～7.4‰,平均值为6.1‰;含矿花岗斑岩δ334SVCDT为4.4‰～6.2‰,平均值为5.7‰;轧轧龙铅锌矿金属硫化物δ334SVCDT为2.7‰～8.3‰,平均值为5.1‰;德新和轧轧龙铅锌矿铅同位素比值比较稳定,变化范围基本一致;铅同位素μ值为9.48～9.82,平均值为9.64;△β、△γ变化范围基本一致,均值相差较小,表明则学地区热液脉型铅锌矿金属硫化物和斑岩具有一致的S、Pb同位素组成,铅同位素具正常铅特征;暗示硫源可能主要由花岗岩类提供,铅源则可能主要来自上地壳物质。综合前人研究认为,德新、轧轧龙热液脉型铅锌矿和纳如松多铅锌矿具有一致的硫、铅同位素组成,三者应存在成因上的联系,可能属于同一成矿系统产物;花岗斑岩为则学地区热液脉状铅锌矿化提供了成矿物质。 相似文献
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Most sulfide-rich magmatic Ni-Cu-(PGE) deposits form in dynamic magmatic systems by partial melting S-bearing wall rocks with variable degrees of assimilation of miscible silicate and volatile components, and generation of barren to weakly-mineralized immiscible Fe sulfide xenomelts into which Ni-Cu-Co-PGE partition from the magma. Some exceptionally-thick magmatic Cr deposits may form by partial melting oxide-bearing wall rocks with variable degrees of assimilation of the miscible silicate and volatile components, and generation of barren Fe ± Ti oxide xenocrysts into which Cr-Mg-V ± Ti partition from the magma. The products of these processes are variably preserved as skarns, residues, xenoliths, xenocrysts, xenomelts, and xenovolatiles, which play important to critical roles in ore genesis, transport, localization, and/or modification. Incorporation of barren xenoliths/autoliths may induce small amounts of sulfide/chromite to segregate, but incorporation of sulfide xenomelts or oxide xenocrysts with dynamic upgrading of metal tenors (PGE > Cu > Ni > Co and Cr > V > Ti, respectively) is required to make significant ore deposits. Silicate xenomelts are only rarely preserved, but will be variably depleted in chalcophile and ferrous metals. Less dense felsic xenoliths may aid upward sulfide transport by increasing the effective viscosity and decreasing the bulk density of the magma. Denser mafic or metamorphosed xenoliths may also increase the effective viscosity of the magma, but may aid downward sulfide transport by increasing the bulk density of the magma. Sulfide wets olivine, so olivine xenocrysts may act as filter beds to collect advected finely dispersed sulfide droplets, but other silicates and xenoliths may not be wetted by sulfides. Xenovolatiles may retard settling of – or in some cases float – dense sulfide droplets. Reactions of sulfide melts with felsic country rocks may generate Fe-rich skarns that may allow sulfide melts to fractionate to more extreme Cu-Ni-rich compositions. Xenoliths, xenocrysts, xenomelts, and xenovolatiles are more likely to be preserved in cooler basaltic magmas than in hotter komatiitic magmas, and are more likely to be preserved in less dynamic (less turbulent) systems/domain/phases than in more dynamic (more turbulent) systems/domains/phases. Massive to semi-massive Ni-Cu-PGE and Cr mineralization and xenoliths are often localized within footwall embayments, dilations/jogs in dikes, throats of magma conduits, and the horizontal segments of dike-chonolith and dike-sill complexes, which represent fluid dynamic traps for both ascending and descending sulfides/oxides. If skarns, residues, xenoliths, xenocrysts, xenomelts, and/or xenovolatiles are present, they provide important constraints on ore genesis and they are valuable exploration indicators, but they must be included in elemental and isotopic mass balance calculations. 相似文献
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Hirokazu Fujimaki 《Contributions to Mineralogy and Petrology》1986,94(1):42-45
Concentration ratios of Hf, Zr, and REE between zircon, apatite, and liquid were determined for three igneous compositions: two andesites and a diorite. The concentration ratios of these elements between zircon and corresponding liquid can approximate the partition coefficient. Although the concentration ratios between apatite and andesite groundmass can be considered as partition coefficients, those for the apatite in the diorite may deviate from the partition coefficients. The HREE partition coefficients between zircon and liquid are very large (100 for Er to 500 for Lu), and the Hf partition coefficient is even larger. The REE partition coefficients between apatite and liquid are convex upward, and large (D=10–100), whereas the Hf and Zr partition coefficients are less than 1. The large differences between partition coefficients of Lu and Hf for zircon-liquid and for apatite-liquid are confirmed. These partition coefficients are useful for petrogenetic models involving zircon and apatite. 相似文献
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《Chemical Geology》2007,236(1-2):13-26
We examined the coprecipitation behavior of Ti, Mo, Sn and Sb in Ca–Al–Mg fluorides under two different fluoride forming conditions: at < 70 °C in an ultrasonic bath (denoted as the ultrasonic method) and at 245 °C using a Teflon bomb (denoted as the bomb method). In the ultrasonic method, small amounts of Ti, Mo and Sn coprecipitation were observed with 100% Ca and 100% Mg fluorides. No coprecipitation of Ti, Mo, Sn and Sb in Ca–Al–Mg fluorides occurred when the sample was decomposed by the bomb method except for 100% Ca fluoride. Based on our coprecipitation observations, we have developed a simultaneous determination method for B, Ti, Zr, Nb, Mo, Sn, Sb, Hf and Ta by Q-pole type ICP-MS (ICP-QMS) and sector field type ICP-MS (ICP-SFMS). 9–50 mg of samples with Zr–Mo–Sn–Sb–Hf spikes were decomposed by HF using the bomb method and the ultrasonic method with B spike. The sample was then evaporated and re-dissolved into 0.5 mol l− 1 HF, followed by the removal of fluorides by centrifuging. B, Zr, Mo, Sn, Sb and Hf were measured by ID method. Nb and Ta were measured by the ID-internal standardization method, based on Nb/Mo and Ta/Mo ratios using ICP-QMS, for which pseudo-FI was developed and applied. When 100% recovery yields of Zr and Hf are expected, Nb/Zr and Ta/Hf ratios may also be used. Ti was determined by the ID-internal standardization method, based on the Ti/Nb ratio from ICP-SFMS. Only 0.053 ml sample solution was required for measurement of all 9 elements. Dilution factors of ≤ 340 were aspirated without matrix effects. To demonstrate the applicability of our method, 4 carbonaceous chondrites (Ivuna, Orgueil, Cold Bokkeveld and Allende) as well as GSJ and USGS silicate reference materials of basalts, andesites and peridotites were analyzed. Our analytical results are consistent with previous studies, and the mean reproducibility of each element is 1.0–4.6% for basalts and andesites, and 6.7–11% for peridotites except for TiO2. 相似文献
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针对兖州煤田下组煤深部开采受奥灰高承压水威胁以及当地大型煤化工企业生产用水量大的现状,在已进行的水文地质勘探及放水试验基础上,评价奥灰富水性,并采用有限差分法进行奥灰疏水降压数值模拟研究,提出水煤共采观点。研究结果表明:兖州煤田深部奥灰水压高,合理布置水煤共采孔,可以实现奥灰水位的有效疏降,疏降中心区水位最大降深可达110 m,突水系数显著下降,提高了下组煤开采的安全性;同时可提供煤化工43200 m3/d的供水量,能达到可持续的、水资源保护性的供水效果,实现下组煤的水煤共采。 相似文献
17.
The distribution of Cu, Co, As and Fe was studied downstream from mines and deposits in the Idaho Cobalt Belt (ICB), the largest Co resource in the USA. To evaluate potential contamination in ecosystems in the ICB, mine waste, stream sediment, soil, and water were collected and analyzed for Cu, Co, As and Fe in this area. Concentrations of Cu in mine waste and stream sediment collected proximal to mines in the ICB ranged from 390 to 19,000 μg/g, exceeding the USEPA target clean-up level and the probable effect concentration (PEC) for Cu of 149 μg/g in sediment; PEC is the concentration above which harmful effects are likely in sediment dwelling organisms. In addition concentrations of Cu in mine runoff and stream water collected proximal to mines were highly elevated in the ICB and exceeded the USEPA chronic criterion for aquatic organisms of 6.3 μg/L (at a water hardness of 50 mg/L) and an LC50 concentration for rainbow trout of 14 μg/L for Cu in water. Concentrations of Co in mine waste and stream sediment collected proximal to mines varied from 14 to 7400 μg/g and were highly elevated above regional background concentrations, and generally exceeded the USEPA target clean-up level of 80 μg/g for Co in sediment. Concentrations of Co in water were as high as in 75,000 μg/L in the ICB, exceeding an LC50 of 346 μg/L for rainbow trout for Co in water by as much as two orders of magnitude, likely indicating an adverse effect on trout. Mine waste and stream sediment collected in the ICB also contained highly elevated As concentrations that varied from 26 to 17,000 μg/g, most of which exceeded the PEC of 33 μg/g and the USEPA target clean-up level of 35 μg/g for As in sediment. Conversely, most water samples had As concentrations that were below the 150 μg/L chronic criterion for protection of aquatic organisms and the USEPA target clean-up level of 14 μg/L. There is abundant Fe oxide in streams in the ICB and several samples of mine runoff and stream water exceeded the chronic criterion for protection of aquatic organisms of 1000 μg/L for Fe. There has been extensive remediation of mined areas in the ICB, but because some mine waste remaining in the area contains highly elevated Cu, Co, As and Fe, inhalation or ingestion of mine waste particulates may lead to human exposure to these elements. 相似文献
18.
Stratiform quartz-sulphide lodes in Ingladhal occur in a typical Precambrian green-stone-belt environment comprising metabasalts, tuff, chert and cherty iron-sulphide formation. Unusually high cobalt contents of metavolcanics and of sulphide minerals in orebodies suggest a consanguinity between ores and rocks. 90% of total nickel, 70% of total cobalt but only 30% of total copper in rocks occur in silicate phases and thus indicate an early separation of copper from cobalt and nickel. Unusually high non-sulphide copper in barren bedded cherts implies availability of Cu-rich solution prior to their lithification. Pyrite in sediments, in volcanics, and in orebodies is characterized by a distinctive pattern of Co-Ni distribution in each case. Partitioning of Co and Ni between coexisting sulphide pairs is complex, but gross equilibrium is indicated. Very high trace metal content of orebody pyrite sharply contrasts with very low such values in pyrite from adjacent sediments and points to a higher temperature of formation of orebodies. 相似文献
19.
A theoretical model was developed to study the chemical speciation of the trace elements Zn, Cd, Cu and Pb aqueous solutions and their responses to variations in ionic strength and complexation. Two mixing solutions were investigated, a freshwater-seawater system and a freshwater-brine system. The brine was a calcium, sodium-chloride solution with a molal ionic strength of two. Trace element associations with the ligands OH?, Cl?, CO2?3, SO2?4, and HCO?3 were considered at pHs from 3.5 to 11.0 at 25°C. In general, the relative importance of the various ligand-trace element complexes can be predicted from a comparison of their stability constants. However, the effect of pH on the importance of a given complex is not readily apparent from the stability constants. Freshwater-seawater mixtures, as might be found in a totally mixed estuary, show that seawater composition is the dominant control on chemical complexing. Chloride complexing is similar for lead and zinc in the freshwater-brine mixtures. This similarity may account in part for the association of lead and zinc in strata-bound ore deposits. 相似文献
20.
The dielectric constants and dielectric loss values of 4 Ca-containing minerals were determined at 1 MHz using a two-terminal method and empirically determined edge corrections. The results are: vesuvianitel κ′ a=9.93 tan δ=0.006 κ′ c=9.79 tan δ=0.005 vesuvianitel κ′ a=10.02 tan δ=0.002 κ′ c=9.85 tan δ=0.003 zoisite1 κ′ a =10.49 tan δ=0.0006 κ′ b =15.31 tan δ=0.0008 κ′ c=9.51 tan δ=0.0008 zoisite2 κ′ a =10.55 tan δ=0.0011 κ′ b =15.45 tan δ=0.0013 κ′ c=9.39 tan δ=0.0008 epidote κ′ 11= 9.52 tan δ=0.0008 κ′ 22=17.1 tan δ=0.0009 κ′ 33= 9.37 tan δ=0.0006 fluorapatite1 κ′ a =10.48 tan δ=0.0008 κ′ c = 8.72 tan δ=0.0114 fluorapatite2 κ′ a =10.40 tan δ=0.0010 κ′ c=8.26 tan δ=0.0178 The deviation (δ) between measured dielectric polarizabilities as determined from the Clausius-Mosotti equation and those calculated from the sum of oxide polarizabilities according to α D (mineral)=∑ α D (oxides) for vesuvianite is ～ 0.5%. The large deviations of epidote and zoisite from the additivity rule with Δ=+ 10.1 and + 11.7%, respectively, are attributed to “rattling” Ca ions. The combined effects of both a large F thermal parameter and possible F-ion conductivity in fluorapatite are believed to be responsible for Δ=+2–3%. Although variation of oxygen polarizability with oxygen molar volume (Vo) is believed to affect the total polarizabilities, the variation of Vo in these Ca minerals is too small to observe the effect. 相似文献