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1.
夏日哈木铜镍矿是在东昆仑造山带首次被发现的岩浆熔离型矿床,该类型矿床是青海省铜镍矿勘查研究方向之一.笔者通过夏日哈木镍矿成矿特征研究认为:碰撞伸展环境是夏日哈木超大型镍-钴硫化物矿形成的基本条件,成岩成矿年龄集中于早泥盆世,岩体侵位于古元古代金水口白沙河组,参与后期混染成矿作用.对柴达木南北缘岩浆熔离型镍矿的成矿条件分析发现:泥盆纪热事件显示柴达木盆地南、北缘在该期均发生了碰撞伸展作用和成矿作用,镁铁质-超镁铁质岩均侵入古老地层,地层硫参与成矿作用;成矿镁铁质-超镁铁质岩体与物探磁异常,Ni、Co、Cu组合异常相对应.综合分析,柴达木南北缘岩浆熔离型镍矿的找矿潜力大,提出了今后柴达木南北缘岩浆熔离型镍矿勘查重点是柴达木南缘的昆中岩浆弧带、柴达木北缘高压变质岩带、欧龙布鲁克陆块. 相似文献
2.
红旗岭铜镍硫化物矿床位于兴-蒙造山带东部。矿区出露30多个镁铁-超镁铁质侵入体,主要由橄榄岩、辉石岩和辉(苏)长岩组成。本文通过对红旗岭含矿镁铁-超镁铁质岩体的主、微量及铂族元素(PGE)的研究,探讨了红旗岭岩体成矿母岩浆性质、PGE亏损的原因以及岩体形成的构造环境。全岩主、微量元素地球化学分析表明,红旗岭岩体具有高MgO(平均28.75%)、低TiO2(平均0.44%),富集轻稀土元素(LREE)、亏损高场强元素(HFSE),极低ΣPGE(平均2.08×10~(-9))和高Cu/Pd(平均2916×10~3)的特征。岩石样品显示相似的微量和PGE配分模式,表明其来源于相同的岩浆源区。根据橄榄石-熔体平衡及质量平衡原理估算出红旗岭母岩浆为高镁玄武质岩浆(MgO=10.74%、FeO=7.78%)。红旗岭母岩浆在早期演化过程中发生硫化物熔离作用导致了红旗岭含矿岩体PGE的极度亏损。结合中亚造山带东段构造演化历史,本文认为红旗岭岩体形成于晚三叠世碰撞后伸展环境,矿床的形成受到了古亚洲洋俯冲结束后板片断离的影响。 相似文献
3.
内蒙古西乌旗格尔楚鲁晚三叠世流纹岩年代学、地球化学特征及其地质意义 总被引：1，自引：0，他引：1
为确定西乌旗格尔楚鲁地区的一套浅色流纹岩的形成时代及其成岩构造环境,进而为探讨古亚洲洋闭合时间提供新的证据,本文对其开展了锆石U-Pb年代学、岩石学和地球化学研究。结果表明,流纹岩形成于221±1Ma;岩石富硅碱、贫钙镁、高Ga/Al值,A/CNK1;轻、重稀土元素分馏不明显,具有显著的Eu负异常;强烈亏损Sr、P、Ti,富集Zr,具有A2型花岗岩的特征,其成因可能是造山后伸展环境下幔源岩浆的底侵和地壳减薄,暗示研究区在三叠纪已经处于伸展背景,古亚洲洋在三叠纪之前已经闭合。研究区三叠纪伸展背景之下的岩浆活动始于早三叠世并一直持续到晚三叠世。 相似文献
4.
陕西略阳煎茶岭镍矿床酸性侵入岩形成时代及成矿意义 总被引：2，自引：0，他引：2
煎茶岭镍矿是一个与镁质超基性岩和酸性侵入岩有关的镍矿床。矿床地质研究发现,矿体主要赋存于花岗斑岩北侧超基性岩体内,矿石中交代状、浸染状、网脉状结构发育,显示热液改造成因矿床的典型结构、构造特征。岩、矿石地球化学及同位素分析表明,煎茶岭镍矿床与典型的镁铁质岩浆硫化物矿床不同,镍矿床在成矿过程中虽继承了超基性岩中的成矿物质,但受到花岗斑岩强烈改造有关,矿床成因类型为岩浆热液改造型。花岗斑岩和钠长斑岩中锆石U-Pb测年表明,花岗斑岩U-Pb年龄为859±26 Ma,钠长斑岩U-Pb年龄为844±26 Ma,认为煎茶岭镍矿成岩成矿时代为新元古代晋宁期,非前人所认为的海西期或印支期,是全球Rodinia超大陆裂解事件在扬子板块西北缘的重要响应。 相似文献
5.
中国镍矿成矿规律初探 总被引：12，自引：0，他引：12
我国镍矿可分为岩浆型、海相沉积型和风化壳型3种预测类型.矿床形成时代较为连续,最早形成于中—新元古代,最晚形成于新生代,其中中—新元古代和晚古生代是形成矿床的两个高峰期;中—新元古代矿床主要分布在华北地块和扬子地块周缘,晚古生代镍矿主要分布在中亚造山带、峨眉山和塔里木大火成岩省范围内.岩浆型镍矿主要形成于大陆边缘裂解、造山带后碰撞伸展以及地幔柱3种构造背景,根据不同构造背景并结合主要岩浆作用特点,将与幔源基性—超基性岩有关的镍-铜-钴-铂族元素矿床成矿系列类型划分出与大陆裂解边缘幔源基性—超基性岩浆作用有关的镍-铜-钴-铂族元素矿床成矿亚类型、与地幔柱基性—超基性岩浆作用有关的镍-铜-钴-铂族元素矿床成矿亚类型、与造山带俯冲作用下幔源基性—超基性岩有关的镍-铜-钴-铂族元素矿床成矿亚类型、与造山带后碰撞伸展背景下幔源基性—超基性岩有关的镍-铜-钴-铂族元素矿床成矿亚类型等4种亚类型.分别对中—新元古代与大陆边缘裂解有关的镍铜(铂)矿床、寒武纪与黑色页岩有关的海相沉积型镍钼钒矿床、早二叠世与造山带伸展背景有关的镍铜矿床、晚二叠世与大火成岩省有关的镍铜(铂)矿床、新生代与风化壳有关的镍金矿床及其对应的典型矿床特征和成矿模式进行了叙述;认为大陆裂解边缘、地幔柱、造山带后碰撞伸展是我国镍矿形成的有利成矿地质背景,与邻近深大断裂、镁铁—超镁铁岩体、高MgO的原生岩浆(高镁玄武质岩浆)、深部岩浆作用、硫饱和与硫化物熔离共同组成岩浆型镍矿的6个重要地质条件. 相似文献
6.
滇东南八布地区发育一套晚古生代超镁铁质-镁铁质杂岩,是认识古特提斯分支洋构造演化的重要窗口,而其中以火山岩为赋矿围岩的杨万铜矿床,被视作区域找矿的突破点。目前,对这套超镁铁质-镁铁质杂岩的构造属性及赋存铜矿床的成矿时代及成因联系还存在争议。通过对杨万铜矿床中黄铜矿和黄铁矿进行Re-Os同位素定年,获得Re-Os等时线年龄为269±3 Ma,表明该矿床形成于早中二叠世,与火山岩(～270 Ma)大致同时;而初始187Os/188Os值为0.31±0.17,暗示成矿时存在热液流体与古海水的相互作用。区内玄武岩围岩和其它超镁铁质-镁铁质岩石的地球化学特征对比分析显示,八布超镁铁质-镁铁质杂岩为一套N-MORB型蛇绿岩组合,代表了古特提斯分支洋盆的洋壳残片。杨万铜矿床应划归为与古特提斯分支洋裂解有关的火山成因块状硫化物(VMS)矿床,其周边地区具有较好的找矿潜力。 相似文献
7.
吉林红旗岭铜镍硫化物矿床的成矿时代讨论 总被引：14，自引：2，他引：12
通过对红旗岭铜镍硫化物矿床1号含矿超镁铁质岩体和8号不含矿镁铁-超镁铁质岩体进行单矿物40Ar-39Ar法测年,得到与铜镍硫化物矿床相关的角闪石与黑云母结晶年龄分别为250 Ma和225 Ma,这一结果与前人所报道的K-Ar法年龄有明显的差异.结合与热液矿化相关的斜长伟晶岩锆石SHRIMP法年龄216 Ma,认为镁铁-超镁铁质岩形成于250 Ma左右的印支早期,铜镍硫化物矿床的形成时间晚于含矿岩体,大约为225 Ma前后的印支中期.216 Ma前后的岩浆期后热液叠加对成矿具有积极作用. 相似文献
8.
寄主岩浆硫化物和氧化物矿床的镁铁质-超镁铁质岩体对比分析与成矿过程评述 总被引：4，自引：2，他引：2
镁铁质-超镁铁质岩体是世界上岩浆硫化物(Ni-Cu-PGE)和氧化物(Fe-Ti-V-P)矿床的主要载体.全球主要岩浆硫化物和氧化物矿床均可以产于大火成岩省、克拉通区的裂谷带或伸展环境、褶皱带内的后碰撞伸展环境.寄主岩浆硫化物矿床的岩体规模相差甚大(从6×104km2到＜0.1km2),既有超镁铁质岩石组合也有镁铁质岩石组合,但其原生岩浆主要为拉斑玄武质岩浆.含镍铜的铂族元素矿床主要赋存于规模很大的层状岩体中,而镍铜硫化物矿床主要赋存于小岩体中.寄主钒钛磁铁矿或磁铁矿矿床的岩体主要是以辉长岩为主的层状杂岩体.寄主钛铁矿-磷灰石矿床的岩体均为层状的斜长岩-纹长二长岩-紫苏花岗岩岩体.尽管其岩石组合相差很大,但其原生岩浆均属拉斑玄武质.寄主硫化物矿床的岩体相对富Si、Mg、Cr、Ni,而寄主氧化物矿床的岩体相对富Fe-Ti-P-V,造岩矿物晶体化学也反映了这种差异.对全球主要含矿岩体的对比分析表明,导致这种反差的主要控制因素应该是岩浆生成时的压力状态,源区性质和熔融程度的差异可能只在局部范围内起作用.对岩浆硫化物矿床成矿过程的认识集中体现在金川模式和岩浆通道模式上,对岩浆氧化物矿床成矿过程的认识体现在氧化物和磷灰石是堆晶相还是从不混溶的矿浆中结晶的.对比分析表明,成矿过程具有多样性,试图用一种模式概括所有同类矿床成矿过程的想法未必可取.毫无疑问,适宜的氧化还原环境是形成岩浆矿床的必要务件,伴随岩浆演化及成矿过程的氧速度变化及其诱因问题尚待进一步探索. 相似文献
9.
内蒙古中部地区横跨中亚造山带与华北克拉通北缘,区内岩浆铜镍硫化物矿床(点)广泛发育。克布矿床位于该区白云鄂博裂谷西南侧,是近年来新发现的品位较高的铜镍化物矿床。因此,准确厘定克布镁铁-超镁铁质岩体的形成时代,查明岩石成因与矿床成矿过程对于进一步指导克布矿床深部铜镍找矿突破以及区域类似镁铁-超镁铁质岩体含矿性评价具有重要意义。克布岩体主要岩相由主体辉长岩相与赋矿橄榄岩相组成,其中辉长岩相属于主体岩相而橄榄岩相则是主要赋矿岩相。岩石地球化学分析结果表明,克布镁铁-超镁铁质岩体各岩相具有轻稀土富集、重稀土亏损的右倾型稀土配分模式,富集Rb、Sr和Ba等元素,亏损Nb和Ta等元素。本次研究获得克布岩体橄榄辉长岩的LA-ICP-MS锆石U-Pb年龄为267.5±1.8Ma,为中二叠世岩浆作用的产物,形成于古亚洲洋闭合后的碰撞后伸展环境。同位素组成研究结果表明,克布岩体锆石εHf(t)值为-4.67～2.84,(87Sr/86Sr)i值为0.7062～0.7071,εNd(t)值为为-10... 相似文献
10.
西北地区是中国岩浆铜镍硫化物矿床最为发育的地区,主要有3个重要成矿期,其地质特点、成矿条件、形成标志等存在明显不同。笔者梳理了目前诸多学者对岩浆铜镍硫化物矿床的研究工作,并结合野外实际,发现大陆裂谷是形成巨型-超大型岩浆铜镍硫化物矿床的构造背景条件,铁质系列的镁铁-超镁铁质岩体才可能形成有经济价值的岩浆铜镍硫化物矿体。超壳深大断裂为地幔岩浆上涌提供了有利条件。分异良好的超基性岩体更具有成铜镍矿的潜力。结晶分异促进了硫化物饱和,地壳混染是成矿的关键。橄榄石和单斜辉石具有低的CaO和FeO含量的岩体,更有利于形成规模较大的岩浆铜镍硫化物矿体。这些研究认识与发现为理解西北地区镁铁-超镁铁质岩浆成矿作用过程、找矿潜力预测及找矿方向和找矿空间提供了技术支撑与资料基础。 相似文献
11.
E. M. Prasolov S. A. Sergeev B. V. Belyatsky E. S. Bogomolov K. A. Gruzdov I. N. Kapitonov R. Sh. Krymsky V. O. Khalenev 《Geochemistry International》2018,56(1):46-64
This paper reports the first results of a study of 11 isotope systems (3He/4He, 40Ar/36Ar, 34S/32S, 65Cu/63Cu, 62Ni/60Ni, 87Sr/86Sr, 143Nd/144Nd, 206–208Pb/204Pb, Hf–Nd, U–Pb, and Re–Os) in the rocks and ores of the Cu–Ni–PGE deposits of the Norilsk ore district. Almost all the results were obtained at the Center of Isotopic Research of the Karpinskii All-Russia Research Institute of Geology. The use of a number of independent genetic isotopic signatures and comprehensive isotopic knowledge provided a methodic basis for the interpretation of approximately 5000 isotopic analyses of various elements. The presence of materials from two sources, crust and mantle, was detected in the composition of the rocks and ores. The contribution of the crustal source is especially significant in the paleofluids (gas–liquid microinclusions) of the ore-forming medium. Crustal solutions were probably a transport medium during ore formation. Air argon is dominant in the ores, which indicates a connection between the paleofluids and the atmosphere. This suggests intense groundwater circulation during the crystallization of ore minerals. The age of the rocks and ores of the Norilsk deposits was determined. The stage of orebody formation is restricted to a narrow age interval of 250 ± 10 Ma. An isotopic criterion was proposed for the ore-bearing potential of mafic intrusions in the Norilsk–Taimyr region. It includes several interrelated isotopic ratios of various elements: He, Ar, S, and others. 相似文献
12.
奥地利安东帕有限公司 《岩矿测试》2009,28(3):306-306
最新的流行病学研究表明,空气中较高浓度的悬浮细颗粒可能对人类的健康有不利的影响。根据该项研究显示,由于心脏病、慢性呼吸问题和肺功能指标恶化而导致死亡率的升高与细尘粒子有关。这些研究结果已经促使欧盟于1999年4月出台了限制空气中二氧化硫、二氧化氮、氧化氮、铅和颗粒物含量的法案(1999/30/EC),对各项指标包括对可吸入PM10颗粒的浓度提出了新的限制性指标。PM10颗粒是指可以通过预分级器分离采集的气体动力学直径小于10μm的细颗粒。目前研究的兴趣重点逐步偏向PM2.5这些更细微颗粒物,PM2.5这种颗粒物对健康有明显的不利影响。在欧盟指令2008/50/EC中,对PM10和PM2.5都提 相似文献
13.
S. Viswanathan K. Surya Prakash Rao B. Mahabaleswar 《Journal of the Geological Society of India》2013,82(6):621-627
Komatiites are mantle-derived ultramafic volcanic rocks. Komatiites have been discovered in several States of India, notably in Karnataka. Studies on the distribution of trace-elements in the komatiites of India are very few. This paper proposes a simple, accurate, precise, rapid, and non-destructive wavelength-dispersive x-ray fluorescence (WDXRF) spectrometric technique for determining Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th in komatiites, and discusses the accuracy, precision, limits of detection, x-ray spectral-line interferences, inter-element effects, speed, advantages, and limitations of the technique. The accuracy of the technique is excellent (within 3%) for Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Zr, Nb, Ba, Pb, and Th and very good (within 4%) for Y. The precision is also excellent (within 3%) for Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th. The limits of detection are: 1 ppm for Sc and V; 2 ppm for Cr, Co, and Ni; 3 ppm for Cu, Zn, Rb, and Sr; 4 ppm for Y and Zr; 6 ppm for Nb; 10 ppm for Ba; 13 ppm for Pb; and 14 ppm for Th. The time taken for determining Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th in a batch of 24 samples of komatiites, for a replication of four analyses per sample, by one operator, using a manual WDXRF spectrometer, is only 60 hours. 相似文献
14.
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
15.
《Applied Geochemistry》2001,16(2):137-159
Five hundred and ninety-eight samples of terrestrial moss (Hylocomium splendens and Pleurozium schreberi) collected from a 188,000 km2 area of the central Barents region (NE Norway, N Finland, NW Russia) were analysed by ICP-AES and ICP-MS. Analytical results for Al, B, Ba, Ca, K, La, Mg, Mn, Na, P, Rb, Si, Sr, Th, U and Y concentrations are reported here. Graphical methods of data analysis, such as geochemical maps, cumulative frequency diagrams, boxplots and scatterplots, are used to interpret the origin of the patterns for these elements. None of the elements reported here are emitted in significant amounts from the smelting industry on the Kola Peninsula. Despite the conventional view that moss chemistry reflects atmospheric element input, the nature of the underlying mineral substrate (regolith or bedrock) is found to have a considerable influence on moss composition for several elements. This influence of the chemistry of the mineral substrate can take place in a variety of ways. (1) It can be completely natural, reflecting the ability of higher plants to take up elements from deep soil horizons and shed them with litterfall onto the surface. (2) It can result from naturally increased soil dust input where vegetation is scarce due to harsh climatic conditions for instance. Alternatively, substrate influence can be enhanced by human activity, such as open-cast mining, creation of ‘technogenic deserts’, or handling, transport and storage of ore and ore products, all of which magnify the natural elemental flux from bedrock to ground vegetation. Seaspray is another natural process affecting moss composition in the area (Mg, Na), and this is most visible in the Norwegian part of the study area. Presence or absence of some plant species, e.g., lichens, seems to influence moss chemistry. This is shown by the low concentrations of B or K in moss on the Finnish and Norwegian side of the (fenced) border with Russia, contrasting with high concentrations on the other side (intensive reindeer husbandry west of the border has selectively depleted the lichen population). 相似文献
16.
Mercury,arsenic, antimony,and selenium contents of sediment from the Kuskokwim River,Bethel, Alaska,USA 总被引：1，自引：0，他引：1
The Kuskokwim River at Bethel, Alaska, drains a major mercury-antimony metallogenic province in its upper reaches and tributaries. Bethel (population 4000) is situated on the Kuskokwim floodplain and also draws its water supply from wells located in river-deposited sediment. A boring through overbank and floodplain sediment has provided material to establish a baseline datum for sediment-hosted heavy metals. Mercury (total), arsenic, antimony, and selenium contents were determined; aluminum was also determined and used as normalizing factor. The contents of the heavy metals were relatively constant with depth and do not reflect any potential enrichment from upstream contaminant sources. 相似文献
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19.
《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
20.
The Samchampi-Samteran alkaline igneous complex (SAC) is a near circular, plug-like body approximately 12 km2 area and is emplaced into the Precambrian gneissic terrain of the Karbi Anglong district of Assam. The host rocks, which
are exposed in immediate vicinity of the intrusion, comprise granite gneiss, migmatite, granodiorite, amphibolite, pegmatite
and quartz veins.
The SAC is composed of a wide variety of lithologies identified as syenitic fenite, magnetite ± perovskite ± apatite rock,
alkali pyroxenite, ijolite-melteigite, carbonatite, nepheline syenite with leucocratic and mesocratic variants, phonolite,
volcanic tuff, phosphatic rock and chert breccia.
The magnetite ± perovskite ± apatite rock was generated as a cumulus phase owing to the partitioning of Ti, Fe at a shallow
level magma chamber (not evolved DI = O1). The highly alkaline hydrous fluid activity indicated by the presence of strongly
alkalic minerals in carbonatites and associated alkaline rocks suggests that the composition of original melt was more alkalic
than those now found and represent a silica undersaturated ultramafic rock of carbonated olivine-poor nephelinite which splits
with falling temperature into two immiscible fractions—one ultimately crystallises as alkali pyroxenite/ijolite and the other
as carbonatite. The spatial distribution of varied lithotypes of SAC and their genetic relationships suggests that the silicate
and carbonate melts, produced through liquid immiscibility, during ascent generated into an array of lithotypes and also reaction
with the country rocks by alkali emanations produced fenitic aureoles (nephelinisation process). Isotopic studies (δ18O and δ13C) on carbonatites of Samchampi have indicated that the δ13C of the source magma is related to contamination from recycled carbon. 相似文献