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雅鲁藏布江蛇绿岩带长1500km以上,分为东段(曲水—墨脱)、中段(昂仁—仁布)和西段(萨嘎以西至中印边境)3部分。西段又进一步分为北亚带(达机翁—萨嘎蛇绿岩带)和南亚带(达巴—休古嘎布蛇绿岩带),以往的研究程度很低。达巴—休古嘎布蛇绿岩带的蛇绿岩体(块)由地幔橄榄岩组成,主要岩石类型是方辉橄榄岩和纯橄榄岩,极少量二辉橄榄岩,缺少典型蛇绿岩剖面中的洋壳单元。带内岩体规模大,岩相分带明显,出现较大面积的纯橄榄岩相。拉昂错、东坡、当穷岩体和休古嘎布岩体群发现有较多的铬铁矿化点,矿体呈透镜状(豆荚状)、短脉状、不规则状,矿石以致密块状为主,少部分为浸染状,Cr2O3含量一般达40%以上。矿化类型属于豆荚状铬铁矿。对比研究显示,该岩带的岩体在构造环境,蛇绿岩的类型,岩体规模,岩石组成,保存部位,部分熔融程度,岩石、矿物地球化学特征,铬铁矿化特征等许多方面与国内外大型豆荚状铬铁矿床的含矿岩体相似,成矿条件好,找矿前景较大。提出区内找矿前景最好的地段是拉昂错岩体西北部的纯橄榄岩相,其次是东坡岩体的纯橄榄岩相、纯橄榄岩-方辉橄榄岩相,以及当穷岩体的方辉橄榄岩-纯橄榄岩相。 相似文献
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错不扎蛇绿岩位于雅鲁藏布江缝合带西段北亚带,岩体呈北西-南东走向带状产出,主要由地幔橄榄岩和辉长岩脉组成。地幔橄榄岩主体为方辉橄榄岩,详细的矿物学及岩石地球化学研究表明,错不扎方辉橄榄岩中橄榄石为镁橄榄石,斜方辉石主要为顽火辉石,而单斜辉石主要为顽透辉石和透辉石,铬尖晶石具有高Al和高Mg(Mg#=60~70)特征。稀土配分图解显示其具有轻稀土亏损而重稀土富集的左倾型亏损地幔源区特征,(La/Yb)N=0.11~0.60,模拟结果显示其为经历了15%~20%部分熔融后的残余,与快速扩张大洋中脊环境下形成的深海橄榄岩的熔融程度(10%~22%)较为一致。此外,错不扎方辉橄榄岩轻稀土含量明显高于部分熔融模型中LREE的含量,而且,在微量元素原始地幔标准化图解中富集大离子亲石元素Rb、Sr和高场强元素Ta、Hf和Ti,这一特征指示错不扎方辉橄榄岩在大洋中脊环境形成后又受到后期俯冲带熔/流体的改造。结合南北两带不同蛇绿岩体构造环境的对比,笔者认为雅鲁藏布江西段南北两带蛇绿岩体具有相似的形成环境,两者在地理位置以及产状方面的差别可能是受到构造侵位的影响。 相似文献
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西藏雅鲁藏布江缝合带西段南北亚带蛇绿岩的成因探讨 总被引：2，自引：2，他引：0
雅鲁藏布江蛇绿岩带自萨嘎以西分为达巴-休古嘎布(南亚带)和萨嘎-达机翁(北亚带)两个亚带,但两者的关系和构造环境还存在争论。本文在实测剖面的基础上,对比南北亚带蛇绿岩产出和岩石组成,以及对比基性岩脉和围岩方辉橄榄岩的地球化学和年代学特征,探讨两个带的关系和构造环境。北带错不扎、加纳崩和巴尔基性岩脉具有高Si、Al,低K、Ti、P特征,属钙碱性玄武质成分,锆石U-Pb年龄为125~128Ma;南亚带东波、普兰、休古嘎布基性岩具有高Mg、Ti,低Si、K特征,为低钾拉斑玄武质成分,锆石U-Pb年龄为120~130Ma。南北带基性岩具有类似产状和年代学,球粒陨石标准化曲线与NMORB一致;N-MORB标准化蛛网图中显示Nb、Ta、Ti负异常,指示洋内俯冲带弧前或弧后环境。此外,两带基性岩围岩方辉橄榄岩中橄榄石、辉石、尖晶石具有类似的矿物成分特征,地球化学成分兼有弧前和深海地幔橄榄岩的特点,指示南北亚带蛇绿岩形成于俯冲带弧前环境。结合区域对比,南亚带蛇绿岩不发育沟-弧-盆体系,具有从北到南的构造侵位特征,南北亚带之间的仲巴微地体具有特提斯喜马拉雅的亲缘性,指示南北蛇绿岩亚带可能为相同大洋岩石圈的不同残余。 相似文献
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达机翁蛇绿岩位于雅鲁藏布江缝合带的西段北亚带,该蛇绿岩主要由地幔橄榄岩、玄武岩以及硅质岩组成,其中地幔橄榄岩以方辉橄榄岩为主,同时含有少量的纯橄榄岩,纯橄岩主要呈不规则透镜状或团块状分布于方辉橄榄岩中。在达机翁地幔橄榄岩中产出有3种不同类型的铬铁矿,分别为块状,豆状以及浸染状铬铁矿。文章主要对达机翁地幔橄榄岩的方辉橄榄岩及豆荚状铬铁矿进行了研究,结合岩石的主量元素和铂族元素,对地幔橄榄岩和豆荚状铬铁矿的成因以及雅鲁藏布江缝合带的找矿远景进行了探讨。达机翁地幔橄榄岩具有较高的Mg O含量以及较低的Al2O3和Ca O等含量,这种亏损的全岩成分指示了达机翁地幔橄榄岩经历了较高的部分熔融作用,同时方辉橄榄岩的PGEs的总量为23.68×10-9~31.02×10-9,高于原始地幔的值,Pd和Cu 2个元素的含量较为分散明显偏离部分熔融曲线,指示了达机翁方辉橄榄岩可能遭受了熔体的改造,在熔体-岩石反应的过程中,导致了富含PPGE的硫化物的加入。达机翁豆荚状铬铁矿为高Cr型铬铁矿,具有IPGE和Rh明显富集以及Pt,Pd明显亏损的特征,不同类型的铬铁矿之间具有一致的PGEs的分配模式。雅鲁藏布江缝合带内大量分布的超镁铁岩体在岩石组合、地球化学特征、成因以及形成时代等方面,均具有相似性,是中国铬铁矿找矿的有利远景区。 相似文献
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雅鲁藏布江蛇绿岩带西段达机翁地幔橄榄岩组成特征及其形成环境分析 总被引：6，自引：5，他引：1
雅鲁藏布江蛇绿岩带自萨嘎以西分成南北两个亚带。对两个亚带蛇绿岩的各自特征及成因联系的研究,是探讨雅鲁藏布江西段的新特提斯洋构造演化的关键。北亚带蛇绿岩呈构造岩块产于冈底斯山前喀喇昆仑断裂带的南侧。其中,位于北亚带西北段的达机翁蛇绿岩,主要由地幔橄榄岩,玄武岩夹硅质岩组成,各单元间断层接触。对达机翁蛇绿岩的地幔橄榄岩开展的组成特征研究表明:(1)地幔橄榄岩主体为方辉橄榄岩,含少量的纯橄岩。方辉橄榄岩内产有豆荚状铬铁矿(呈豆状,块状以及浸染状),铬铁矿有一层纯橄岩的外壳;(2)达机翁方辉橄榄岩单斜辉石含量低,组成矿物以及全岩的地球化学特征均指示了这些样品经历了相对高的部分熔融作用;(3)方辉橄榄岩具有U型的球粒陨石标准化的稀土元素分配模式,Nb相对亏损,Ta,Zr和Hf具有弱的正异常,同时Sr和U具有强烈的正异常,这些特征可能与残余地幔和俯冲带熔/流体之间相互作用导致的轻稀土元素和部分微量元素的选择性富集有关。定量计算表明,达机翁地幔岩中的方辉橄榄岩来源于一个尖晶石相地幔源区的部分熔融,部分熔融程度大于25%,高于深海地幔橄榄岩的部分熔融程度(10%~22%)。这些橄榄岩形成时的氧逸度条件位于FMQ和FMQ+1之间,高于深海地幔橄榄岩(FMQ-1),与俯冲带环境的氧逸度条件一致。因此,我们认为达机翁蛇绿岩中的地幔橄榄岩形成于大洋中脊的环境,随后发生了洋内俯冲作用,位于俯冲带上部的地幔橄榄岩经历了俯冲带流/熔体的交代作用。 相似文献
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雅鲁藏布江缝合带西段北亚带的基性岩成因和构造意义 总被引：5，自引：0，他引：5
雅鲁藏布江蛇绿岩带自萨嘎以西分为达巴—休古嘎布(南亚带)和达机翁—萨嘎(北亚带)两个亚带,但两者的成因和构造背景还不清楚。本文在研究北亚带加纳崩—错不扎基性岩脉的年代学和地球化学及对比南亚带的基础上,探讨了两个带的成因和关系问题。加纳崩辉长岩和错不扎辉绿岩呈脉状或长透镜状产在方辉橄榄岩中,宽1~3 m不等,走向北西。两者的锆石U-Pb年龄分别为(125.8±2.6)Ma和(127.0±0.5)Ma。岩石地球化学均具有高Si、Al、Na、Mg和低Ti、K、P的特征,属钙碱性玄武质成分。球粒陨石标准化曲线与N-MORB一致;N-MORB标准化蛛网图中显示Nb、Ta、Ti负异常,判断两者形成于大洋俯冲的弧前或弧后环境。对比前人研究,南亚带普兰、东波和休古嘎布蛇绿岩中的基性岩具有相同产状和时代(120~130 Ma),地球化学特征也同样显示形成于洋内俯冲带环境。结合两带基性岩的围岩地幔橄榄岩均具有弧前环境特征,初步认为南北蛇绿岩亚带可能是相同构造背景的大洋岩石圈残余。 相似文献
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皖南蛇绿岩带位于江南造山带北东段,该区地幔橄榄岩多已发生蚀变甚至全部蛇纹石化,成为制约该区深部研究工作的一个现实瓶颈.为查明该蛇绿岩及赋存其中的伏川铬铁矿床的成因,本研究通过电子显微镜以及电子探针等手段,对皖南蛇绿岩和不同类型铬铁矿石（Ⅰ类以铬绿泥石为主要脉石矿物和Ⅱ类以异剥辉石为主要脉石矿物）中铬铁矿及其共生矿物进行深入研究,发现铬铁矿为典型的阿尔卑斯型高铝型铬铁矿,大多发育裂隙结构,在颗粒边缘或裂隙处部分蚀变为铁铬铁矿.对铬铁矿核部未蚀变部分进行研究,得出方辉橄榄岩中铬尖晶石Cr#（100×Cr/（Cr+Al））为54.12~65.18,Mg#（100×Mg/（Mg+Fe2+））为42.37~54.84,铬铁矿石中铬铁矿Cr#为53.97~62.29,Mg#为59.49~68.57.铬铁矿母岩浆成分和MORB（mid-ocean ridge basalt）基本一致,表明伏川铬铁矿结晶时母岩浆的成分可能为MORB.对其氧化环境的研究发现其成岩成矿环境为低氧逸度（-0.14至+0.68log（QFM））,并具有从MORB向SSZ（suprasubduction zone）过渡的特征.结合野外地质现象,认为铬铁矿石可能是地幔橄榄岩和洋中脊玄武岩浆反应而形成,而方辉橄榄岩又体现出SSZ特征,说明皖南蛇绿岩应该是地幔橄榄岩部分熔融、岩石-熔体反应和板块俯冲等综合作用的结果,这为研究江南造山带的构造和演化提供重要依据. 相似文献
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丁青蛇绿岩体位于班公湖—怒江缝合带东段,该缝合带与雅鲁藏布江缝合带并列,是寻找我国铬铁矿床的重要地区。该蛇绿岩体呈近南东向展布,总面积近600 km2,主要由地幔橄榄岩、辉石岩、辉长岩、辉绿岩、玄武岩、斜长花岗岩、硅质岩和泥质岩组成。根据空间分布,丁青蛇绿岩分为东、西两个岩体。在前人工作基础上,通过地质填图、实测剖面、探槽和钻孔编录,共发现豆荚状铬铁矿矿点83处,其中东岩体27处,西岩体56处。根据铬铁矿产出和围岩特征,丁青铬铁矿可分为4种产出类型。类型I:矿体呈脉状产出,围岩为条带状或透镜状纯橄榄岩和块状方辉橄榄岩;类型II:矿体呈透镜状、豆荚状或不规则团块状产出,围岩为薄壳状纯橄榄岩和斑杂状或块状方辉橄榄岩;类型III:矿体呈浸染状弥散分布于纯橄榄岩中,围岩为条带状纯橄榄岩和块状或斑杂状方辉橄榄岩;类型IV:矿体呈条带状产出,围岩为条带状或透镜状纯橄榄岩和具定向结构的方辉橄榄岩。根据矿石构造特征,主要分为块状、脉状、浸染状、浸染条带状4种类型。块状和脉状铬铁矿为矿石的主要类型,少量为浸染状和浸染条带状,局部纯橄榄岩中发育极少量瘤状或豆状构造。本研究选择了13处代表性铬铁矿点开展了详细的岩石学、矿相学、矿物学和矿物化学等工作。根据矿石中铬尖晶石的矿物化学特征,可将丁青铬铁矿矿体分为高铬(Cr#=78～86)、中高铬(Cr#=60～74)、中铬(Cr#2=30～51)和低铬(Cr#=9～14)4种类型(Cr#=100×Cr/(Cr+Al))。丁青东岩体赋存有中高铬型和中铬型铬铁矿,缺少高铬型铬铁矿;西岩体赋存有高铬型和中铬型铬铁矿,缺少中高铬型铬铁矿。同时在丁青东、西岩体内均发现存在一种Cr#极低的铬铁矿,暂定为"低铬型铬铁矿"。这些不同类型的铬铁矿体与野外产出有一定的对应关系,也可能后者制约了它们的成因。与罗布莎岩体中的典型高铬型铬铁矿对比,丁青豆荚状铬铁矿在矿物组合和矿物化学成分等方面具有许多相似性,认为存在较大的找矿空间。 相似文献
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Petrology and Geochemistry of the Dangqiong Ophiolite,Western Yarlung-Zangbo Suture Zone,Tibet,China
The Dangqiong ophiolite, the largest in the western segment of the Yarlung-Zangbo Suture Zone(YZSZ)ophiolite belt in southern Tibet, consists of discontinuous mantle peridotite and intrusive mafic rocks. The former is composed dominantly of harzburgite, with minor dunite, locally lherzolite and some dunite containing lenses and veins of chromitite. The latter, mafic dykes(gabbro and diabase dykes), occur mainly in the southern part. This study carried out geochemical analysis on both rocks. The results show that the mantle peridotite has Fo values in olivine from 89.92 to 91.63 and is characterized by low aluminum contents(1.5–4.66 wt%) and high Mg# values(91.06–94.53) of clinopyroxene. Most spinels in the Dangqiong peridotites have typical Mg# values ranging from 61.07 to 72.52, with corresponding Cr# values ranging from 17.67 to 31.66, and have TiO2 contents from 0 to 0.09%, indicating only a low degree of partial melting(10–15%). The olivine-spinel equilibrium and spinel chemistry of the Dangqiong peridotites suggest that they originated deeper mantle(20 kbar). The gabbro dykes show N-MORB-type patterns of REE and trace elements. The presence of amphibole in the Dangqiong gabbro suggests the late-stage alteration of subduction-derived fluids. All the lherzolites and harzburgites in Dangqiong have similar distribution patterns of REE and trace elements, the mineral chemistry in the harzburgites and lherzolites indicates compositions similar to those of abyssal and forearc peridotites, suggesting that the ophiolite in Dangqiong formed in a MOR environment and then was modified by late-stage melts and fluids in a suprasubduction zone(SSZ) setting. This formation process is consistent with that of the Luobusa ophiolite in the eastern Yarlung-Zangbo Suture Zone and Purang ophiolite in the western Yarlung-Zangbo Suture Zone. 相似文献
12.
《International Geology Review》2012,54(9):1105-1123
ABSTRACTA chromite deposit was discovered in the Kudi ophiolite in the Palaeozoic western Kunlun orogenic belt. Chromite forms elongated (<2 m in width) and banded chromitite bodies (<0.1 m in width for each band) in dunite and podiform chromitite bodies (<1.5 m in width) in harzburgite. Dunite is classified into two types. Type I dunite hosting massive and banded chromitites shows low Fo in olivine (88.1–90.9), moderate Cr# [=Cr/(Cr + Al), 0.47–0.56] in chromite, and a positively sloped primitive mantle-normalized platinum group elements (PGE) pattern, suggesting that it is a cumulate of a mafic melt. Harzburgite and type II dunite show olivine with high Fo (>91.1) and chromite with moderate to high Cr# (0.44–0.61), and flat to negatively sloped primitive mantle-normalized PGE patterns, indicating that they are residual mantle peridotite after partial melting. Chromite in all three types of chromitites has relatively uniform moderate values Cr# ranging from 0.43 to 0.56. Massive chromitite contains euhedral chromite with high TiO2 (0.40–0.43 wt.%) and has a positively sloped primitive mantle-normalized PGE pattern, suggesting that it represents a cumulate of a melt. Rocks containing disseminated and banded chromite show overall low total PGE, < 117 ppb, and a negatively sloped primitive mantle-normalized PGE pattern. Chromite grains in these two types of occurrences are irregular in shape and enclose olivine grains, suggesting that chromite formed later than olivine. We suggest that chromite-oversaturated melt penetrated into the pre-existing dunite and crystallized chromite. The oxygen fugacity (fO2 values of chromitites and peridotites are high, ranging from FMQ+0.8 (0.8 logarithmic unit above the fayalite-magnetite-quartz buffer) to FMQ+2.3 for chromitites and from FMQ+0.9 to FMQ+2.8 for peridotites (dunite and harzburgite). The mineral compositions and high fO2 values as well as estimated parental magma compositions of the chromitites suggest that the Kudi ophiolite formed in a sub-arc setting. 相似文献
13.
M. El Ghorfi F. Melcher T. Oberthür A. E. Boukhari L. Maacha A. Maddi M. Mhaili 《Mineralogy and Petrology》2008,92(1-2):59-80
Summary The Neoproterozoic Bou Azzer ophiolite complex hosts numerous, small lenticular bodies of massive and disseminated chromite.
Metallurgical-grade high-Mg and high-Cr spinels (cores with 48–62 wt% Cr2O3) reveal complex alteration patterns of successive Cr and Mn enrichment and loss of Al towards the rims, while the Mg# ratios
[(Mg/(Mg + Fe2+)] remain almost constant. Concentration patterns of platinum-group elements are typical for ophiolitic chromitite poor in
sulfides, with predominance of the IPGE, variable Rh, and low Pt and Pd. The most abundant platinum-group mineral is Rh-bearing
laurite that occurs either included in spinel or in silicate matrix, whereas Os-Ir-Ru alloy is always included in spinel.
Laurite inclusions reveal complex intergrowth textures with Rh-Ru-Pt rich alloy, and with Rh-rich sulfide. Most laurites display
trends to sulfur-poor compositions leading to local formation of very fine-grained Ru-Os-Ir alloy phases. Ni-Co-Fe sulfides,
arsenides and sulfarsenides devoid of PGE are associated with the alteration of chromite. Textural position and chemical composition
of the base metal inclusions, as well as comparison of alteration features between chromite and accessory chromian spinel
in the Co-Ni-As ores of the Bou Azzer ophiolite indicate a close connection. It is suggested that hydrothermal fluids percolated
through the marginal zones of the ophiolite belt during greenschist facies metamorphism and deposited Ni-Co-Fe arsenides,
sulfarsenides and minor sulfides as accessories within altered chromitites, and also in structurally favourable zones as Ni-Co-As
ores.
Author’s address: Dr. Frank Melcher, Federal Institute for Geosciences and Natural Resources, Stilleweg 2, 30655 Hannover, Germany 相似文献
14.
Alteration Mechanisms of Chromian-Spinel during Serpentinization at Wadi Sifein Area, Eastern Desert, Egypt 总被引：1，自引：0，他引：1
Wadi Sifein podiform chromite deposits, Central Eastern Desert of Egypt, are hosted by fully serpentinized peridotite that is a part of the dismembered Pan‐African ophiolite complexes. Relics of primary minerals and the chemical characters indicate that the ophiolitic rocks were derived from depleted mantle peridotite of harzburgite and subordinate dunite compositions. The mantle rocks were initially formed at a mid‐oceanic ridge and subsequently thrust at a supra‐subduction zone. The chromite mineralization at Wadi Sifein area displays either pod‐shaped bodies with massive and lumpy chromitite appearance or dissemination of chromian‐spinel in serpentinite matrix. The podiform chromitite exhibits a very limited compositional range in terms of Cr# [Cr/(Cr + Al) atomic ratio] and Mg# [Mg/(Mg + Fe) atomic ratio]. The chromian‐spinel, however, frequently displays optical and geochemical zoning. Four zones can be identified from core to edge: inner core representing the original composition of the chromian‐spinel; narrow Cr‐rich ferritchromit zone; wide ferritchromit zone; and outer Cr‐magnetite/magnetite zone. The zonation of chromian‐spinel is interpreted to be a result of serpentinization rather than magmatic or metamorphic processes. The geochemical data obtained from the chromitite and chromian‐spinel was statistically processed using discriminant and R‐mode factor analyses. Two trends, minor and major, were achieved considering the formation of ferritchromit. The minor trend is controlled by the redistribution of trivalent cations, where Cr2O3 increased on the expense mainly of Al2O3 and to less extent Fe2O3 to form zone II during the peak of serpentinization. The major trend of alteration, however, is explained by the exchange between Mg‐Fe2+ rather than Cr, Al, and Fe3+ to form zone III. Kammererite formation was accompanied the formation of zones III and IV at a 314°C temperature of formation. 相似文献
15.
The Yarlung Zangbo suture zone (YZSZ) in southern Tibet includes the remnants of Neo‐Tethyan oceanic lithosphere and marks a major suture between the Indian plate to the south and the Lhasa terrane of Tibet to the north. The upper mantle section of the Cuobuzha ophiolite in the northern subbelt of the western YZSZ comprises mainly clinopyroxene (cpx)‐rich and depleted harzburgites. Spinels in the cpx‐harzburgites show lower Cr# values (12.6–15.1) than the spinels in the harzburgites (26.1–34.5), and the cpx‐harzburgites display higher heavy rare earth element concentrations than the depleted harzburgites. The harzburgites have subchondritic Os isotopic compositions (0.11624–0.11699), yielding Re‐depletion model ages (TRD) ages from 1.8 to 1.7 Ga, indicating that the Cubuzha mantle underwent at least one ancient melt extraction event ca. 1.8‐1.7Ga; whereas the cpx‐harzburgites have suprachondritic 187Os/188Os ratios (0.12831–0.13125) with higher Re concentrations (0.380–0.575 ppb), indicating subsequent addition of Re following the last partial melting event that occurred during mid‐ocean ridge melt evolution processes. Although these geochemical and isotopic signatures suggest that both peridotite types in the ophiolite represent mid‐oceanic ridge–type upper mantle units, their melt evolution trends reflect different mantle processes. The cpx‐harzburgites formed from low‐degree partial melting of a primitive mantle source, and they were subsequently modified by melt‐rock interactions in a mid‐oceanic ridge environment. The depleted harzburgites, however, were produced by remelting of the cpx‐harzburgites, which later interacted with mid‐oceanic ridge basalt– or island‐arc tholeiite–like melts, possibly in a trench–distal backarc spreading center. Our new isotopic and geochemical data from the Cuobuzha peridotites confirm that the Neo‐Tethyan upper mantle had highly heterogeneous Os isotopic compositions as a result of multiple melt production and melt extraction events during its seafloor spreading evolution. 相似文献
16.
The Wenquan ultramafic rocks, located in the East Kunlun Orogenic belt in the northeastern part of the Qinghai‐Tibet Plateau, consist of dunite, wehrlite, olivine‐clinopyroxenite and clinopyroxenite, and exhibit cumulate textures. Olivine from dunite has high Fo (forsterite, 90–92) and NiO (0.15–0.42 wt%) contents. Cr‐spinels from all of the rocks in this suite are characterized by high Cr# (100×[Cr/(Cr+Al)], 67–91), low Mg# (100×[Mg/(Mg+Fe2+)], 17–35) and low TiO2 contents (mostly < 0.5 wt%). Clinopyroxenes display high Mg# (92–98) and low TiO2 contents (0.002–0.099 wt%), similar to those in ophiolitic cumulates. Geochemically, the Wenquan ultramafic rocks show enrichment of LILE, Sr, and Ba, and depletion of Nb and Th. Mineral chemistry and geochemistry indicate that the Wenquan cumulates were generated from a depleted mantle and likely evolved from high‐Mg basaltic magmas (Mg#=78) that underwent fractional crystallization and crustal contamination. Zircons from clinopyroxenites yield a U–Pb weighted mean age of 331 ± 2 Ma, which is nearly coeval with the formation age of the Buqingshan and A'nyemaqen Carboniferous ophiolites. The Wenquan Carboniferous ophiolites are confirmed to exist in the Central East Kunlun Fault zone, whereas previous studies have considered them to be the Proterozoic ophiolites. The Wenquan ultramafic rocks might be an arc cumulates of the Paleo‐Tethyan ocean, indicating that there were two cycles of oceanic–continental evolution along the Central East Kunlun Fault zone. Keywords Ultramafic rock, Cumulate, Ophiolite, East Kunlun Orogenic belt. 相似文献
17.
Dunite and serpentinized harzburgite in the Cheshmeh-Bid area, northwest of the Neyriz ophiolite in Iran, host podiform chromitite that occur as schlieren-type, tabular and aligned massive lenses of various sizes. The most important chromitite ore textures in the Cheshmeh-Bid deposit are massive, nodular and disseminated. Massive chromitite, dunite, and harzburgite host rocks were analyzed for trace and platinum-group elements geochemistry. Chromian spinel in chromitite is characterized by high Cr~#(0.72-0.78), high Mg~#(0.62–0.68) and low TiO_2(0.12 wt%-0.2 wt%) content. These data are similar to those of chromitites deposited from high degrees of mantle partial melting. The Cr~# of chromian spinel ranges from 0.73 to 0.8 in dunite, similar to the high-Cr chromitite, whereas it ranges from 0.56 to 0.65 in harzburgite. The calculated melt composition of the high-Cr chromitites of the Cheshmeh-Bid is 11.53 wt%–12.94 wt% Al_2O_3, 0.21 wt%–0.33 wt% TiO_2 with FeO/MgO ratios of 0.69-0.97, which are interpreted as more refractory melts akin to boninitic compositions. The total PGE content of the Cheshmeh-Bid chromitite, dunite and harzburgite are very low(average of 220.4, 34.5 and 47.3 ppb, respectively). The Pd/Ir ratio, which is an indicator of PGE fractionation, is very low(0.05–0.18) in the Cheshmeh-Bid chromitites and show that these rocks derived from a depleted mantle. The chromitites are characterized by high-Cr~#, low Pd + Pt(4–14 ppb) and high IPGE/PPGE ratios(8.2–22.25), resulting in a general negatively patterns, suggesting a high-degree of partial melting is responsible for the formation of the Cheshmeh-Bid chromitites. Therefore parent magma probably experiences a very low fractionation and was derived by an increasing partial melting. These geochemical characteristics show that the Cheshmeh-Bid chromitites have been probably derived from a boninitic melts in a supra-subduction setting that reacted with depleted peridotites. The high-Cr chromitite has relatively uniform mantle-normalized PGE patterns, with a steep slope, positive Ru and negative Pt, Pd anomalies, and enrichment of PGE relative to the chondrite. The dunite(total PGE = 47.25 ppb) and harzburgite(total PGE =3 4.5 ppb) are highly depleted in PGE and show slightly positive slopes PGE spidergrams, accompanied by a small positive Ru, Pt and Pd anomalies and their Pdn/Irn ratio ranges between 1.55–1.7 and 1.36-1.94, respectively. Trace element contents of the Cheshmeh-Bid chromitites, such as Ga, V, Zn, Co, Ni, and Mn, are low and vary between 13–26, 466–842, 22-84, 115–179, 826–-1210, and 697–1136 ppm, respectively. These contents are compatible with other boninitic chromitites worldwide. The chromian spinel and bulk PGE geochemistry for the Cheshmeh-Bid chromitites suggest that high-Cr chromitites were generated from Cr-rich and, Ti-and Al-poor boninitic melts, most probably in a fore-arc tectonic setting related with a supra-subduction zone, similarly to other ophiolites in the outer Zagros ophiolitic belt. 相似文献
18.
西藏雅鲁藏布江缝合带西段发现高铬型和高铝型豆荚状铬铁矿体 总被引：11，自引：5，他引：6
豆英状铬铁矿按其矿物化学组分分为高铝型(Cr#值为20～ 60)和高铬型(Cr#值为60～80)两类(Thayer,1970),在全球已报道的豆英状铬铁矿中普遍为在一岩体内只存一种类型的矿体,而在同一岩体内发现两种类型的铬铁矿体较少见.位于雅鲁藏布江缝合带西段普兰岩体中首次发现同时存在高铬型和高铝型铬铁矿,岩体由地幔橄榄岩、辉长辉绿岩、火山岩等组成.地幔橄榄岩主要为方辉橄榄岩、纯橄岩和少量二辉橄榄岩.在方辉橄榄岩中发现7处透镜状的铬铁矿矿体露头,矿石类型主要有致密块状、稠密浸染状和稀疏浸染状等.矿体长2～6m,厚0.5～2m,矿体的最大延伸方向为北西-南东向,与岩体的展布方向一致,矿石的Cr#=52～88,高铬型铬铁矿包括Cr-2～5矿体,Cr#值为63～89,高铝型铬铁矿有Cr-1和Cr-6矿体,Cr#=52 ～55.矿石中脉石矿物主要为橄榄石、角闪石、蛇纹石等.普兰地幔橄榄岩的矿物结构显示,岩体经历了强烈的部分熔融以及塑性变形作用,地幔橄榄岩的地球化学特征显示岩体形成于MOR,后受到SSZ环境的改造.并且依据铬尖晶石-橄榄石/单斜辉石的矿物化学成分,识别出普兰地幔橄榄岩至少经历了3次不同的部分熔融,包括早期部分熔融(～10％)、晚期部分熔融(20％～30％)和局部的减压部分熔融作用(～15％).对比其他铬铁矿矿体和地幔橄榄岩的矿物组合,矿物化学和地球化学等,显示普兰豆荚状铬铁矿矿体与典型高铬型、高铝型铬铁矿具相似性,并存在较大的找矿空间. 相似文献
19.
泽当蛇绿岩位于雅鲁藏布江缝合带东段,岩体由地幔橄榄岩、辉长辉绿岩、辉石岩、火山岩等组成。地幔橄榄岩主要为方辉橄榄岩、纯橄岩和二辉橄榄岩。在方辉橄榄岩中发现7处豆荚状铬铁矿,矿石类型主要有致密块状和浸染状。出露地表的长度0.5~3m,厚0.2~1m。矿体的延伸方向为北西向,与岩体展布的方向一致,铬铁矿的Cr~#=67.9~88.5,属于高铬型铬铁矿。泽当地幔橄榄岩岩相学特征以及矿物组合、矿物化学成份及岩相学特征,显示岩体至少存在两次的部分熔融过程,即为早期的MOR构造背景,以及后期SSZ环境的改造。铬铁矿的铂族元素(PGE)以富集Os、Rh、Pd,亏损Ir、Ru、Pt的负斜率分布模式,表明其形成过程中经受后期熔体/流体的改造。对比罗布莎岩体的矿物组合,矿物化学和地球化学等特征,显示泽当豆荚状铬铁矿矿体与典型高铬型具相似性,存在较大的找矿空间。 相似文献