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1.
Associated with the Cretaceous Okorusu carbonatite complex (Namibia) is a hydrothermal fluorite mineralization hosted in Pan-African country rock marbles, which resulted from fluid-rock reaction between the marbles and orthomagmatic, carbonatitic fluids expelled from the carbonatite. Yellow fluorite I was deposited in veins up to 5 cm away from the wallrock contact, followed by purple and colorless fluorite II, smoky quartz and barite, a Mn-rich crust on early calcite, and pure calcite. This clear-cut sequence of mineral growth allows an investigation into fluid-rock interaction processes between the marble and the migrating carbonatitic fluid, and element fractionation patterns between the fluid and subsequent hydrothermal precipitates.Fluorite I shows a progressive change in color from dark yellow to colorless with purple laminations over time of deposition. Subsequent fluorite I precipitates show an increase in Ca, and a continuous decrease in F, Sr, REE, Y, Th, U and Pb contents. The ratios (Eu/Eu*)cn, Th/Pb and U/Pb increase whereas Y/Ho, Th/U and (La/Yb)cn decrease. The Sr-isotopic composition remains constant at 87Sr/86Sr = 0.70456-0.70459, but with varying, highly radiogenic Pb (206Pb/204Pb = 32-190, 238U/204Pb = 7-63). Fluorite II has 87Sr/86Sr = 0.70454-0.70459, 206Pb/204Pb = 18.349, and 207Pb/204Pb = 15.600, and a chemical composition similar to youngest fluorite I. The Mn-rich crust on early calcite accumulated REE, Ba, Pb, Zr, Cs, Th and U, developing into pure calcite with a prominent negative Ce anomaly and successively more radiogenic Sr. The calculated degrees of fluid-rock interaction, f = weight fraction of fluid/(fluid + marble), decrease from fluorite I and most fluorite II (f = 0.5) to calcite (f = 0.2-0.3) and hydrothermal quartz (f ? 0.1). A crush-leach experiment for fluid inclusions in the hydrothermal quartz yielded a Rb-Sr isochron age of 103 ± 12 Ma. Crush-leach analysis for the carbonatitic fluid trapped in the wallrock yielded a trend from the fluid leachate to the host quartz (206Pb/204Pb = 18.224 and 18.602, 207Pb/204Pb = 15.616 and 15.636, respectively) extending from carbonatite towards crustal rocks.Calculated trace element distribution coefficients fluorite/fluid are below unity throughout, and increase from La to Yb. Elements largely excluded from fluorite (Ba, Pb, LREE relative to HREE) were incorporated later into the Mn-rich crust on calcite. The trace element patterns of the hydrothermal minerals are related to changing aCO2 and aF− in the fluid during continued fluid-marble reaction. A predominance of carbonate over fluoride complexing in the fluid as reactions proceeded controlled the Y/Ho, Th/U and REE patterns in the fluid and the crystallizing phases. Deviations from these trends indicate discontinuous processes of fluid-rock reaction. 相似文献
2.
The geochemistry of carbonatites and related rocks from two carbonatite complexes,south Nyanza,Kenya
Christopher Barber 《Lithos》1974,7(1):53-63
Carbonatites, metasomatised country rocks, and carbonatitic calcite and magnetite have been analysed from two carbonatite complexes, Homa and Wasaki, W. Kenya.The carbonatites are all greatly Ce-earth enriched, contain abundant ‘carbonatitic’ trace elements (Sr, Ba, Nb and REE), and generally low concentrations of Cr, Co, Ni, Pb, Ga, Ge, Sn, Bi, Li and Mo. At both complexes early søvite is rich in Sr, and impoverished in other trace elements relative to the alvikites. The late-intruded melacarbonatites contain the greatest concentrations of Ba, REE, Fe and Mn.It is concluded that the accumulation of these elements in the later carbonatites is mainly due to fractionation of carbonates from carbonatite magma which was initially rich in ‘carbonatitic’ trace elements. 相似文献
3.
碳酸岩岩浆作用过程的包裹体研究 总被引：3，自引：0，他引：3
碳酸岩是一种富含碳酸盐矿物(方解石，白云石，铁白云石等＞50％以上)的火成岩。通常以侵入的方式，与超基性岩和碱性岩共生，位于环状侵人体的中心部位；或以喷出的方式，与碱性岩等构成环状杂岩体。碳酸岩在喷出或侵入过程中，与上部地壳围岩发生以富含碱质(钠或钾)为主的蚀变作用，形成特征性的蚀变岩石——霓长岩。通过对碳酸岩中的包裹体研究，可以获得包括成岩成矿时的温度、压力、密度、流体组分、流体演化等大量信息。碳酸岩矿物中包裹体的研究已取得很大进展，并为了解碳酸岩岩浆演化性质和特征提供了许多重要的信息：(1)碳酸岩可以形成于流体和熔体两种介质条件下；(2)碳酸岩矿物中包裹体富含CO2；(3)在碳酸岩的起源和演化过程中伴随有岩浆的不混溶作用发生；(4)碳酸岩岩浆具有的较低的粘度和密度。为了保证对从碳酸岩中获得的包裹体资料的合理解释，在研究过程中必须结合碳酸岩产出的大地构造背景、典型岩石组合、典型蚀变岩石(霓长岩)、赋存的矿产特征等方面的资料。虽然目前在包裹体研究方面尚有许多不足，但作为自然界唯一能够保存有原始成岩成矿流体的地质样品，包裹体的研究具有其他方法不可替代的作用。 相似文献
4.
Tibor Guzmics Roger H. Mitchell Csaba Szabó Márta Berkesi Ralf Milke Rainer Abart 《Contributions to Mineralogy and Petrology》2011,161(2):177-196
Kerimasi calciocarbonatite consists principally of calcite together with lesser apatite, magnetite, and monticellite. Calcite
hosts fluid and S-bearing Na–K–Ca-carbonate inclusions. Carbonatite melt and fluid inclusions occur in apatite and magnetite,
and silicate melt inclusions in magnetite. This study presents statistically significant compositional data for quenched S-
and P-bearing, Ca-alkali-rich carbonatite melt inclusions in magnetite and apatite. Magnetite-hosted silicate melts are peralkaline
with normative sodium-metasilicate. On the basis of our microthermometric results on apatite-hosted melt inclusions and forsterite–monticellite
phase relationships, temperatures of the early stage of magma evolution are estimated to be 900–1,000°C. At this time three
immiscible liquid phases coexisted: (1) a Ca-rich, P-, S- and alkali-bearing carbonatite melt, (2) a Mg- and Fe-rich, peralkaline
silicate melt, and (3) a C–O–H–S-alkali fluid. During the development of coexisting carbonatite and silicate melts, the Si/Al
and Mg/Fe ratio of the silicate melt decreased with contemporaneous increase in alkalis due to olivine fractionation, whereas
the alkali content of the carbonatite melt increased with concomitant decrease in CaO resulting from calcite fractionation.
Overall the peralkalinity of the bulk composition of the immiscible melts increased, resulting in a decrease in the size of
the miscibility gap in the pseudoquaternary system studied. Inclusion data indicate the formation of a carbonatite magma that
is extremely enriched in alkalis with a composition similar to that of Oldoinyo Lengai natrocarbonatite. In contrast to the
bulk compositions of calciocarbonatite rocks, the melt inclusions investigated contain significant amount of alkalis (Na2O + K2O) that is at least 5–10 wt%. The compositions of carbonatite melt inclusions are considered as being better representatives
of parental magma composition than those of any bulk rock. 相似文献
5.
At Oricola (Aquila-Abruzzo, Italy) carbonatite is associated with phonolitic foidite tuff. The Oricola carbonatite contains fresh silicate glass of kamafugitic foidite composition which, compared with carbonate, shows similar trace element patterns but lower concentrations. As a whole, the mineralogy of the Oricola rocks matches that of the neighbouring Grotta del Cervo kamafugitic foidite and carbonatitic foidite and is in the range of the Intramountain Ultralkaline Province (IUP) of melilitites and carbonatites of Italy.
The IUP carbonatites and kamafugitic foidites definitely form intra-outcrop conjugate pairs. All these co-eruptive rocks have parallel trace element patterns, namely REE, which implies a dilution–concentration relationship among them but always with higher contents in primary calcite. Based on current textural and compositional criteria, as well as comparable experimental data, we attribute this feature to liquid immiscibility dominant over crystal fractionation at crustal pressure. This relatively late immiscibility phenomenon is superimposed on co-magmatic features shown by inter-outcrop conjugate rock couples. In fact if we consider San Venanzo kamafugite and Polino Ca-carbonatite, or Grotta del Gervo kamafugite and Oricola Ca-carbonatite, we note couple by couple that they are chemical heteromorphs erupted in isolation in different place. The REE distribution is another distinctive feature of these couples and shows a marked crossover at MREE level. A fact we interpret as produced by near mantle-solidus immiscibility. After this early phenomenon the two members of the couple can erupt in a near primary state carrying mantle xenoliths or undergo some evolution including settling out mantle xenoliths and crystals and fractionation and finally exsolve a carbonatitic residuum by immiscibility. 相似文献
6.
Natrocarbonatite flows in the crater of the volcano Oldoinyo Lengai (Tanzania) are the only carbonatite magmas observed to erupt and have provided strong arguments in favor of a magmatic origin for carbonatite. The currently favored explanation for the genesis of these carbonatites by liquid immiscibility between a silicate and a carbonatite melt is questioned based on the extremely low eruption temperatures of 544-593 °C and compositional and mineralogical characteristics not in agreement with experimental constraints. Experimental investigations of the relationship between Oldoinyo Lengai natrocarbonatite and related silicate rock compositions do indicate that alkali-bearing peralkaline carbonatite with liquidus calcite can form by liquid immiscibility. At the same time, these experiments result in evidence which speaks against a liquid immiscibility origin for the highly alkaline and peralkaline Oldoinyo Lengai natrocarbonatite. On the carbonatite side of the miscibility gap, fractional crystallization cannot account for a liquid evolution from alkali-bearing peralkaline carbonatite to highly alkaline natrocarbonatite. Such an evolution does not seem to be compatible with the liquidus mineral assemblages and the chemistry of Oldoinyo Lengai natrocarbonatite. No natural silicate magma is known to produce natrocarbonatite compositions by liquid immiscibility. The best interpretation of the Oldoinyo Lengai natrocarbonatite flows involves expulsion of a cognate, mobile, alkaline, and CO2-rich fluid condensate. This conclusion is supported by recent studies of silicate and carbonatite melt inclusions in minerals of ultramafic alkaline complexes, trace element partitioning, isotopic constraints, and by experimental data on major element partitioning between coexisting H2O-CO2-rich fluid and carbonatitic melt. In contrast to all other suggested modes of formation, an origin of Oldoinyo Lengai natrocarbonatite from cognate fluid appears best to be in agreement with the field observations, the petrography, mineralogy, and geochemistry of Oldoinyo Lengai natrocarbonatite and the dynamics of the Oldoinyo Lengai natrocarbonatite extrusion. 相似文献
7.
The Huanglongpu carbonatite-related Mo ore field is located in the Lesser Qinling Orogenic belt in the southern margin of the North China block. The ore field is composed of six deposits, Yuantou, Wengongling, Dashigou, Shijiawan, Taoyuan and Erdaohe, all of which are genetically related to carbonatite dykes except for the Shijiawan deposit which is associated with a granitic porphyry. The Yuantou carbonatite dykes intruded into Archean gneiss and other carbonatites emplaced into Mesoproterozoic volcanic and sediment rocks. The carbonatites are mainly composed of calcite and variable amounts of quartz and K-feldspar and minor molybdenite. Re–Os dating of molybdenite from the Yuantou carbonatite yields a weighted average age of 225.0 ± 7.6 Ma, consistent with the molybdenite age (221 Ma) from the Dashigou deposit. The rocks are characterized by high heavy REE (HREE) contents and consistent flat REE distribution patterns with La/Ybcn ~ 1. Quartz in the carbonatites from Yuantou and Dashigou deposits shows consistent O isotopes (8.1–10.2‰) similar to the associated calcite (7.2–9.5‰). The quartz and associated K-feldspar contain lower Zr, Hf and higher HREE abundances and negligible Eu anomaly relative to those from the granite porphyry in Shijiawan. Both minerals are primary products in the carbonatitic liquid, and not captured from the wall-rocks or crustal-derived silicate magmas, or a hydrothermal origin. Thus, the Huanglongpu carbonatitic liquids were enriched in Si and Mo, which may be produced by intensely fractional crystallization of non-silicate minerals. 相似文献
8.
The variant rock types of an Alkaline-Carbonatite Complex (ACC) comprising alkali pyroxenite, nepheline syenite, phoscorite, carbonatite, syenitic fenite and glimmerite along with REE and Nb-mineralization are found at different centres along WNW-ESE trending South Purulia Shear Zone (SPSZ) in parts of Singhbhum Crustal Province. The ACC occurs as intrusions within the Mesoproterozoic Singhbhum Group of rocks. Alkali pyroxenite comprises of aegirine augite, magnesiotaramite, magnesiokatophorite as major constituents. Pyrochlore and eucolite are ubiquitous in nepheline syenite. Phoscorite contains fluorapatite, dahllite, collophane, magnetite, hematite, goethite, phlogopite, calcite, sphene, monazite, pyrochlore, chlorite and quartz. Coarse fluorapatite shows overgrowth of secondary apatite (dahllite). Secondary apatite is derived from primary fluorapatite by solution and reprecipitation. The primary fluorapatite released REE to crystallize monazite grains girdling around primary apatite. Carbonatite is composed dominantly of Srcalcite along with dolomite, tetraferriphlogopite, phlogopitic biotite, aegirine augite, richterite, fluorapatite, altered magnetite, sphene and monazite. The minerals comprising of the carbonatite indicate middle stage of carbonatite development. Fenite is mineralogically syenite. Glimmerite contains 50–60% tetraferriphlogopite. An alkali trend in the evolution of amphiboles (magnesiotaramite-magnesiokatophorite-richterite) and chinopyroxenes (aegirine augite, aegirine) during the crystallization of the suite of rocks is noted. Monazite is the source of REE in phoscorite and carbonatite. Fluorapatite has low contents of REE, PbO, ThO2 and UO2. Pyrochlore reflects Nb-mineralization in nepheline syenite and it is enriched in Na2O, CaO, TiO2, PbO and UO2. Pyrochlore containing UO2 (6.605%) and PbO (0.914%) in nepheline syenite has been chemically dated at 948 ± 24 Ma by EPMA. 相似文献
9.
白云鄂博含矿碱性火山岩建造及其地球化学 总被引：3，自引：1，他引：2
白云鄂博矿床历经几十年的研究,主要集中在矿区H8岩性段矿化白云岩成因的认识,许多研究显示含矿白云岩是岩浆碳酸岩,本文主要从岩石学和地球化学方面进一步分析其属于火山喷发环境形成的火山碳酸熔岩。H8含矿白云岩段和H9板岩段作为一套含矿岩系主要由含矿白云岩、霓闪钠长岩、钾长板岩3类岩石组成,白云岩和霓闪钠长岩都具有的碎屑结构及角砾状构造、条带构造,显示为火山熔岩和火山碎屑岩特征,而钾长板岩则主要显示致密微晶火山熔岩特征。工业矿物主要是磁铁矿、赤铁矿、稀土矿物和铌铁矿物,其重要特征是出现大量原生赤铁矿,反映岩石氧化系数高,与火山喷发环境一致。霓闪钠长岩、钾长板岩岩石化学显示碱性特征,稀土元素与CaO、F相关系数在0.7以上,并与Fe2O3高氧化物相关,而与硅酸盐矿物组分反相关,表示碳酸岩与稀土成矿密切相关,并显示为表生氧化环境形成。稀土地球化学特征显示白云岩∑REE最高,钾长板岩∑REE最低,相应的岩脉∑REE低于喷发岩。各种岩石均表现为明显的轻重稀土分异,但是以白云岩LREE/HREE比值最大,霓闪钠长岩LREE/HREE比值最小,而纯钠长石岩脉和含稀土磁铁矿LREE/HREE明显高于其他岩石。白云岩和霓闪钠长岩均表现出不同的铕、铈负异常,但是碳酸岩脉和钾长板岩则显示弱正铈异常,霓闪钠长岩和钾长板岩铕异常不明显。矿化白云岩和碳酸岩脉的δ18O、δ13C值介于沉积灰岩与已知碳酸岩的δ18O、δ13C值之间,碳酸岩中白云石的δ18O低于方解石的δ18O,而δ13C高于方解石的δ13C,稀土矿物的δ13C、δ18O与碳酸岩脉δ13C、δ18O接近。归纳这些特征,含矿白云岩与霓闪钠长岩、钾长板岩是碱性火山岩组合,与一系列同期的碳酸岩、霓闪钠长岩碱性岩脉一起,构成一套完整碱性火山岩系。 相似文献
10.
岩浆(型)碳酸岩研究进展 总被引：19，自引：0，他引：19
主要从岩石学，矿物学，岩石分类，C，O，Sr同位素，碳酸岩与矿化的关系等各方面对（碱性）碳酸岩的研究进行了较为全面的总结，并结合近20年来实验岩石等，流体包裹体研究，CO2^- H2O－NaCl流体体系的性质的研究，对碳酸岩岩浆的来源及成因，岩浆－热液的演化进行了分析和探讨，碳酸岩形成至少经历了三个阶段，即岩浆阶段，岩浆期后阶段（气相碳酸岩／岩浆热液阶段），交代碳酸岩阶段，而作为与碳酸岩在空间和成因上有密切联系的基性，超基性岩，碱性岩杂岩体，则经历了碳酸岩成岩阶段以前的岩浆不混熔作用，结晶分异作用，岩浆结晶作用以及碳酸岩形成之后的围岩蚀变（霓长岩化）作用。 相似文献
11.
《Journal of Asian Earth Sciences》2002,20(2):127-140
Carbonatites are often of economic importance, which raises the problem of distinguishing carbonatites from limestones when either are metamorphosed to high-grade marbles. They can be of similar appearance, particularly those from the Proterozoic and Archaean of the Indian Subcontinent. This study also contributes to solving the problem of determining the frequency of alkaline and carbonatitic magmatism during the early history of the Earth.The mineral assemblage of apatite–magnetite–phlogopite–calcite is common to marbles of both carbonatite and limestone origin. If pyrochlore is present that identifies the rock as carbonatite; if anorthite, fassaite, scapolite or spinel then it was formerly a limestone. If these minerals are absent, then trace element analysis can supply the critical Sr and REE data, which are both normally high in carbonatitic rocks and low in former limestones. These distinguishing factors are applied to the metamorphic carbonate, pyroxenite, calcite–apatite rock complex at Borra, Eastern Ghats, India, which has been variously interpreted as formerly a carbonatite and as a limestone. The evidence shows that the Borra rocks are meta-sedimentary. 相似文献
12.
本文对白云鄂博地区广泛分布的磷灰石进行了系统的电子探针分析。结果表明,赋矿粗粒白云石大理岩中磷灰石的矿物化学特征与碳酸岩岩墙中的非常相似,它们均属于富含锶和稀土元素的氟磷灰石,具有典型的火成碳酸岩特征。然而,它们在稀土元素分布模式以及轻稀土元素之间的分馏作用方面却存在着差异。造成这些差异的原因是,磷灰石的寄主岩石受富含氟和稀土元素的流体影响的程度不同：粗粒白云石大理岩受流体的影响比碳酸岩岩墙要大。 相似文献
13.
野外调查发现西藏类乌齐地区分布着众多的含镍碳酸岩体,呈十几米至几百米不等的岩株出露。岩体与超基性岩之间具明显的港湾状、枝状侵入接触、岩石不具层理、岩石表现出细粒结晶等粒结构、岩体内见超基性岩捕掳体等特征均表明其为火成碳酸岩岩体。在成分上以菱镁矿为主,岩石中MgO的含量为27.16%~31.75%,为镁质碳酸岩。岩石稀土元素配分曲线呈平缓右倾的轻稀土富集型,轻重稀土元素分馏现象明显,具有明显的Eu正异常和弱的Ce负异常;微量元素显示Rb、Th、Nb、Hf元素相对富集,K、U、Ti元素相对亏损。含镍碳酸岩可能是富CO2的深部流体在中下地壳对超基性岩交代的结果,具备寻找硫化镍矿床的有利条件。 相似文献
14.
《Geochimica et cosmochimica acta》1999,63(3-4):489-508
Lanthanide tetrad effects are often observed in REE patterns of more highly evolved Variscan peraluminous granites of mid-eastern Germany (Central Erzgebirge, Western Erzgebirge, Fichtelgebirge, and Northern Oberpfalz). The degree of the tetrad effect (TE1,3) is estimated and plotted vs. K/Rb, Sr/Eu, Eu/Eu1, Y/Ho, and Zr/Hf. The diagrams reveal that the tetrad effect develops parallel to granite evolution, and significant tetrad effects are strictly confined to highly differentiated samples. Mineral fractionation as a cause for the tetrad effect is not supported by a calculated Rayleigh fractionation, which also could not explain the fractionation trends of Sr/Eu and Eu/Eu1. The strong decrease of Eu concentrations in highly evolved rocks suggests that Eu fractionates between the residual melt and a coexisting aqueous high-temperature fluid. Mineral fractionation as a reason for the tetrad effect is even more unlikely as REE patterns of accessory minerals display similar tetrad effects as the respective host rocks. The accessory minerals inherit the REE signature of the melt and do not contribute to the bulk-rock tetrad effect via mineral fractionation. These results point in summary to significant changes of element fractionation behavior in highly evolved granitic melts: ionic radius and charge, which commonly control the element distribution between mineral and melt, are no longer the exclusive control. The tetrad effect and the highly fractionated trace element ratios of Y/Ho and Zr/Hf indicate a trace element behavior that is similar to that in aqueous systems in which chemical complexation is of significant influence. This distinct trace element behavior and the common features of magmatic-hydrothermal alteration suggest the increasing importance of an aqueous-like fluid system during the final stages of granite crystallization. The positive correlation of TE1,3 with bulk-rock fluorine contents hints at the importance of REE fluorine complexation in generating the tetrad effect. As the evolution of a REE pattern with tetrad effect (M-type) implies the removal of a respective mirroring REE pattern (W-type), the tetrad effect identifies open system conditions during granite crystallization. 相似文献
15.
采取了皖北任楼煤矿太原组灰岩和灰岩水样品进行稀土元素测试分析,结果显示灰岩样品稀土总量较低,平均为36.947×10-6,灰岩样品稀土配分模式表现为轻稀土富集、重稀土亏损型;灰岩水样品稀土总量平均为0.052 6×10-6,灰岩水样品轻、重稀土均富集,轻、重稀土之间分异明显。对灰岩含水层水岩相互作用进行研究,结果表明:轻稀土表现稳定,重稀土分异明显,尤其在Y处有一个明显的峰值;Y元素与Ca元素呈正相关关系,相比石灰岩,灰岩水的Y/Ho、Y/Dy分异更为明显。研究认为,灰岩水中Y元素的峰值效应也可作为灰岩水源识别的依据。 相似文献
16.
The Eocene (ca. 55–38 Ma) Bear Lodge alkaline complex in the northern Black Hills region of northeastern Wyoming (USA) is host to stockwork-style carbonatite dikes and veins with high concentrations of rare earth elements (e.g., La: 4140–21000 ppm, Ce: 9220–35800 ppm, Nd: 4800–13900 ppm). The central carbonatite dike swarm is characterized by zones of variable REE content, with peripheral zones enriched in HREE including yttrium. The principle REE-bearing phases in unoxidized carbonatite are ancylite and carbocernaite, with subordinate monazite, fluorapatite, burbankite, and Ca-REE fluorocarbonates. In oxidized carbonatite, REE are hosted primarily by Ca-REE fluorocarbonates (bastnäsite, parisite, synchysite, and mixed varieties), with lesser REE phosphates (rhabdophane and monazite), fluorapatite, and cerianite. REE abundances were substantially upgraded (e.g., La: 54500–66800 ppm, Ce: 11500–92100 ppm, Nd: 4740–31200 ppm) in carbonatite that was altered by oxidizing hydrothermal and supergene processes. Vertical, near surface increases in REE concentrations correlate with replacement of REE(±Sr,Ca,Na,Ba) carbonate minerals by Ca-REE fluorocarbonate minerals, dissolution of matrix calcite, development of Fe- and Mn-rich gossan, crystallization of cerianite and accompanying negative Ce anomalies in secondary fluorocarbonates and phosphates, and increasing δ18O values. These vertical changes demonstrate the importance of oxidizing meteoric water during the most recent modifications to the carbonatite stockwork. Scanning electron microscopy, energy dispersive spectroscopy, and electron probe microanalysis were used to investigate variations in mineral chemistry controlling the lateral complex-wide geochemical heterogeneity. HREE-enrichment in some peripheral zones can be attributed to an increase in the abundance of secondary REE phosphates (rhabdophane group, monazite, and fluorapatite), while HREE-enrichment in other zones is a result of HREE substitution in the otherwise LREE-selective fluorocarbonate minerals. Microprobe analyses show that HREE substitution is most pronounced in Ca-rich fluorocarbonates (parisite, synchysite, and mixed syntaxial varieties). Peripheral, late-stage HREE-enrichment is attributed to: 1) fractionation during early crystallization of LREE selective minerals, such as ancylite, carbocernaite, and Ca-REE fluorocarbonates in the central Bull Hill dike swarm, 2) REE liberated during breakdown of primary calcite and apatite with higher HREE/LREE ratios, and 3) differential transport of REE in fluids with higher PO43−/CO32− and F−/CO32− ratios, leading to phosphate and pseudomorphic fluorocarbonate mineralization. Supergene weathering processes were important at the stratigraphically highest peripheral REE occurrence, which consists of fine, acicular monazite, jarosite, rutile/pseudorutile, barite, and plumbopyrochlore, an assemblage mineralogically similar to carbonatite laterites in tropical regions. 相似文献
17.
The apatite-bearing carbonate rocks at Eppawala, Sri Lanka occur as massive, discontinuous bodies in a Precambrian, high-grade metamorphic terrain, which weather to form economically important phosphate deposits. The ore bodies at Eppawala contain =42% P 2O 5, and citric acid solubility of different components varies from 4 to 6%. The parent rocks are mainly made up of calcite, dolomite and apatite, with lesser amounts of ilmenite, magnetite, pyrite, forsterite, phlogopite, enstatite, magnesite, diopside, tremolite and spinel. Most of minerals show an euhedral habit, with a wide range of crystal sizes (from a few millimetres to several decimetres). The Eppawala rocks are characterised by low silica (=0.41%), high phosphorous (=10.58%) and high strontium content (2,960–6,819 ppm). Concentrations of light rare-earth elements in these rocks are comparably higher than those of marbles. The REE fractionation of these rocks is pronounced, and La/Yb ratios vary between 14 and 43. Both apatite and calcite show markedly elevated strontium levels (=0.6%). The d 13C PDB and d 18O SMOW values of the carbonates are in the range of –3.4 to –2.2 and 7.7 to 16.4‰ respectively. The euhedral habit, as well as the presence of major quantities of apatite and considerable amounts of iron-bearing minerals suggest that the ore host rock has genetic links to an igneous source rather than to an intensely metamorphosed limestone. The higher light REE contents of the rocks, compared to marbles, also argue against a metamorphic or sedimentary origin. The Sr/Mn and Ce/La ratios in the apatite are ~40 and ~2 respectively, suggesting that they were formed in a carbonatite magma. The markedly increased REE concentrations in the bulk chemistry of the rocks have been shown to be mainly controlled by the content of phosphate minerals. Compared to most carbonatites, the Eppawala rocks are generally depleted in selected trace elements, particularly Ba, Nb, Th, V, U and Zr. This depletion may be due to either a primary infertility of the parent magma with regard to such trace elements, or it is a result of fractional crystallisation during the rock formation. The stable isotope ratios do not plot within the defined "mantle carbonatite box", but still lie within the broader range of carbonatitic rocks. With these data at hand, it can be readily argued that the mode of occurrence, petrography and geochemistry of the Eppawala apatite-bearing carbonates provide conclusive evidence of their carbonatitic origin. 相似文献
18.
L. N. Kogarko 《Geology of Ore Deposits》2014,56(4):230-238
The distribution of radioactive elements in alkaline rocks from Polar Siberia and Ukraine shows that U and Th are markedly concentrated in carbonatite complex and nepheline syenite as final products of magma fractionation. Peralkaline nepheline syenites from Polar Siberia are characterized by very high contents of radioactive elements, which are close to the economic level. Radioactive elements are also concentrated in rocks of the carbonatite complex. For example, some soevites contain up to 294 × 10?4%U and 916 × 10?4% Th. In late dolomite carbonatites, the contents of radioactive elements are appreciably lower. The Th/U ratio in alkaline rocks of Polar Siberia is close to the chondrite value in primary high-Mg rocks and increases in late derivatives: phoscorite, calcite and dolomite carbonatites. The main amount of radioactive elements is contained in rare-metal accessory minerals: perovskite, pyrochlore, calzirtite, and apatite. Rock-forming minerals are distinguished by very low concentrations of radioactive elements. In alkaline series of the Chernigovka massif (Ukraine), U and Th also accumulate in the course of crystal fractionation, especially in phoscorites from the carbonatite complex. Mantle xenoliths and alkaline rocks from Ukraine reveal uranium specialization. Most likely, the discrepancy in fractionation of radioactive elements between Polar Siberia and Ukraine is caused by different geodynamic regimes of these provinces. The Mesozoic alkaline magmatism of Polar Siberia is a part of the Siberian superplume, whereas the Proterozoic alkaline complex in Ukraine is related to subduction of the oceanic crust. 相似文献
19.
白云鄂博碳酸岩墙的稀土和微量元素地球化学及对其成因的启示 总被引：11，自引：1，他引：11
根据矿物组成白云鄂博矿区的碳酸岩岩可墙可分为白云石型、白云石－方解石共存型和方解石型三种类型。REE和微量元素地球化学表明，这三类碳酸岩岩墙为碳酸岩浆演化不同阶段的产物，白云石型和白云石－方解石共存型对应于早期岩浆阶段，其（La/Nd)n、(La/Yb)n比值随稀土总量的增加而增大，方解石型则对应于碳酸岩浆演化的晚期热液阶段，其稀土总量明显富集，但其（La/Nd)n、(La/Y)n和（La/Yb)n比值随稀土总量的增加却有减小的趋势，热液阶段也是白云鄂博稀土矿化的主要阶段。 相似文献
20.
I. L. Nedosekova E. A. Belousova V. V. Sharygin B. V. Belyatsky T. B. Bayanova 《Mineralogy and Petrology》2013,107(1):101-123
The carbonatites of the Ilmeny-Vishnevogorsky Alkaline Complex (IVAC) are specific in geological and geochemical aspects and differ by some characteristics from classic carbonatites of the zoned alkaline-ultramafic complexes. Geological, geochemical and isotopic data and comparison with relevant experimental systems show that the IVAC carbonatites are genetically related to miaskites, and seem to be formed as a result of separation of carbonatite liquid from a miaskitic magma. Appreciable role of a carbonate fluid is established at the later stages of carbonatite formation. The trace element contents in the IVAC carbonatites are similar to carbonatites of the ultramafic-alkaline complexes. The characteristic signatures of the IVAC carbonatites are a high Sr content, a slight depletion in Ba, Nb, Та, Ti, Zr, and Hf, and enrichment in HREE in comparison with carbonatites of ultramafic-alkaline complexes. This testifies a specific nature of the IVAC carbonatites related to the fractionation of a miaskitic magma and to further Late Paleozoic metamorphism. Isotope data suggest a mantle source for IVAC carbonatites and indicate that moderately depleted mantle and enriched EMI-type components participated in magma generation. The lower crust could have been involved in the generation of the IVAC magma. 相似文献