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1.
A total of 17 alkali basalts (alkali olivine basalt, limburgite, olivine nephelinite) and quartz tholeiites, and of 10 peridotite xenoliths (or their clinopyroxenes) were analyzed for Nd and Sr isotopes. 143Nd/144Nd ratios and 87Sr/86Sr ratios of all basalts and of the majority of ultramafic xenoliths plot below the mantle array with a large variation in Nd isotopes and a smaller variation in Sr isotopes. The tholeiites were less radiogenic in Nd than the alkali basalts. Volcanics from the Eifel and Massif Central regions contain Nd and Sr, which is more radiogenic than that of the basalts from the Hessian Depression. Nd and Sr isotopic compositions of all rocks from the latter area, with the exception of one tholeiite and one peridotite plot in the same field of isotope ratios as the Ronda ultramafic tectonite (SW Spain), which ranges in composition from garnet to plagioclase peridotite. The alkali basaltic rocks are products of smaller degrees of partial melting of depleted peridotite, which has undergone a larger metasomatic alteration compared with the source rock of tholeiitic magmas. For the peridotite xenoliths such metasomatic alteration is indicated by the correlation of their K contents and isotopic compositions. We assume that the upper mantle locally can acquire isotopic signatures low in radiogenic Nd and Sr from the introduction of delaminated crust. Such granulites low in radiogenic Nd and Sr are products of early REE fractionation and granite (Rb) separation.  相似文献   

2.
Tholeiites accompanying a majority of alkali basalts are restricted to the highly productive central part of the CECV plume activity in Vogelsberg and Hessian Depression. They mainly occur as quartz tholeiites which according to experiments of partial melting and material balances are products of olivine tholeiitic primary melts. The differentiation from olivine to quartz tholeiitic melts took place in lower crustal magma chambers where olivine tholeiitic melt intruded due to a density comparable with that of the country rocks. The fractionation due to separation of olivine and some clinopyroxene caused contamination of tholeiite magmas by tonalitic partial melts from the wall rocks of the magma chambers. The latter process is indicated by relatively high Rb, K and Pb and low Nb concentrations and by Nd, Sr and Pb isotopes. Contaminating crustal melts, which roughly attained a proportion of 10%, contained very low 143Nd/144Nd ratios from a Nd/Sm fractionation as old as 2.6 Ga. This is the first evidence from mafic rocks of this high age in the lower crust beneath Central Europe. Modelling with incompatible elements allows to recognize olivine tholeiites as products of about 1% partial melting of plume rocks consisting of 35% primitive and 65% depleted mantle materials. The production of tholeiites other than alkali basalts is restricted to the highest plume activity and the largest fraction of MORB type source rocks. Received: 10 December 1999 / Accepted: 23 June 2000  相似文献   

3.
Island chains off western Kyushu are the surface exposure in the northern margin of the Taiwan–Sinzi Folded Zone that spreads along the arc–trench system in the back-arc side from SW Japan to Taiwan. Intermittent igneous activity between the Middle Miocene and Holocene occurred on these islands and widely covered or intruded sedimentary rocks of Early–Middle Miocene. Geochemistry of the volcanic rocks from the Hirado, Ikitsuki and Takushima islands believed to relate to the back-arc opening along the East China and Japan Seas shows a temporal change in source material. Submarine to sub-aerial volcanism occurred on Hirado Island at 15 Ma during the final opening stage of the East China Sea producing tholeiitic basalt and associated andesite–dacite. These eruptives show low incompatible element contents and high FeO*/MgO ratios and reflect a tholeiitic differentiation trend. High Sr and Pb and low Nd isotopic ratios suggest the involvement of EM2-like lithospheric mantle and crustal material in the formation of these syn-opening volcanic rocks. Post-opening alkali basalt volcanism occurred at 9–6 Ma on the islands is characterized by OIB-like higher large ionic lithophile elements (LILE) and high field strength elements (HFSE) compared to 15 Ma basalts in this region and Quaternary basalts along the volcanic front. They have variable range of incompatible element concentrations and ratios along with variable Sr, Pb and Nd isotopic ratios suggesting the involvement of both lithospheric and asthenospheric sources at variable melting degrees (from 4% to less than 15%). The observation that the isotopic compositions of Quaternary alkali basalts south of the studied area are even more depleted suggests an increase in the involvement of asthenospheric source with time.  相似文献   

4.
碳酸岩Sr、Nd、Pb 同位素地球化学研究评述   总被引：3，自引：0，他引：3  
碳酸岩是出露相对较少的幔源岩石，其中Sr与Nd是研究地幔物质组成的主要对象之一。本文统计了世界上主要碳酸岩的锶、钕、铅同位素组成特征；研究显示，碳酸岩源区主要是洋岛玄武岩高U／Pb的HIMU端员和富集端员(EM1或EM2)的混合作用；此外大部分碳酸岩的锶、钕同位素落在大洋玄武岩范围内；这些均表明其成因与地慢柱有密切联系。碳酸岩及与之共生的硅酸岩的同源或独立源区模式部很难充分解释两者同位素组成特征，逭反映碳酸岩的演化模式涉及更复杂的过程。可能是俯冲作用使碳酸岩源区经历不同时间和程度的富集、亏损过程导致地幔源区成分不均一。  相似文献   

5.
Cretaceous-Paleogene granitoid rocks and contemporaneous volcanic rocks are widely distributed in the Inner Zone of Southwest Japan. This intense intermediate to felsic magmatism is considered to have taken place on the eastern margin of the Eurasian Continent, before the Southwest Japan Arc drifted away from the continent in the middle Miocene, resulting in the opening of the Japan Sea. The granitoid rocks show regional variations in terms of their radiometric age, petrography, Sr, Nd and O isotope ratios. Based on Sr and Nd isotope ratios, granitoid rocks can be divided into three zones (South, Transitional and North) between the Median Tectonic Line and the Japan Sea. Granitoid rocks and associated gabbros of the North Zone have low initial Sr isotope ratios (0.7048 to 0.7068) and high initial Nd values (+3 to-2.2), whereas granitoid rocks and gabbros from the South Zone have high initial Sr isotope ratios (0.7070 to 0.7088) and low initial Nd values (-3.0to-8.0). Most granitoid rocks from the Transitional Zone have Sr and Nd isotope ratios that lie between those of the North and South Zones, although there is some overlap. Contamination of magmas by upper crust cannot explain this geographical variation in Sr and Nd isotopes. Instead, the regional variation is attributed to compositionally different, magma sources (probably upper mantle and lower crust), beneath the North and South Zones. This is supported by the Sr and Nd isotopic ratios of upper mantle and lower crustal xenoliths included in Cenozoic volcanic rocks in the North and South Zones. These ratios are similar to those of the granitoid rocks in the respective zones. It is suggested that a micro-continent or island arc consisting of continental crust was underthrust beneath the South Zone before or during the Cretaceous, resulting in compositionally distinct sources for granitoid rocks of the North and South Zones. The large variation observed in Sr and Nd isotope ratios for Transitional Zone granitoid rocks is explained by variable proportions of the two different crustal and upper mantle components.  相似文献   

6.
The Mt. Erciyes stratovolcano was built up in an intraplate tectonic environment as a consequence of Eurasian and Afro-Arabian continental collision. However, the volcanic products generally exhibit a calc-alkaline character; minor amounts of tholeiitic basalts are also present. Tholeiitic basalts show high Fe2O3, MgO, CaO, low K2O, and depleted Ba, Nb, and especially Rb (2.3-5.97 ppm) contents, low 87Sr/86Sr (0.703344-0.703964), and high 143Nd/144Nd (0.512920-0.512780) isotopic ratios. These compositional features show that they were derived from a depleted asthenospheric mantle source, possibly a MORB-like source component. In contrast, calc-alkaline basaltic rocks exhibit relatively high large-ion-lithophile and high-field-strength elements, high 87Sr/86Sr (0.704591-0.70507) and low 143Nd/144Nd (0.51272-0.512394) isotopic ratios.

The bulk-rock chemistry of the tholeiitic basalts reflects the chemical composition of the extracted source component. Furthermore, trace-element concentrations may be calculated from an accepted mantle source component (starting composition) for different degrees of partial melting. These calculations also provide a sensitive approach to the origin of tholeiitic basalts. Modeled trace-element compositions of tholeiitic basalts are calculated from a primitive mantle composition. Calculated trace-element compositions imply that tholeiitic basalts are derived by minor fractional melting (1-1.5 %), in the absence of assimilation or deep-crustal melting. The calc-alkaline basalts were subsequently produced from initially tholeiitic basalts by the way of an AFC (assimilation-fractional crystallization) process, with a crustal assimilation of 10-15 %.

The geochemical data, partial melting, and AFC modeling all indicate that basaltic products have a complex evolutionary history involving partial melting from a MORB-like mantle source. The assimilation and fractional crystallization processes are considered as providing an example for the chemical evolution of basaltic products, from tholeiitic to calc-alkaline, in an intraplate environment.  相似文献   

7.
The reasons for the isotopic heterogeneity of the mantle are analyzed in this paper on the basis of published isotopic data. It was shown that the observed variations in the Sr, Nd, Hf, and Pb isotopic compositions of oceanic basalts cannot be explained by mixing of a finite number of homogeneous reservoirs (components). The considerable variations in the contents of Rb, Sr, Sm, Nd, Lu, Hf, U, Th, and Pb and ratios of these and other trace elements in tholeiitic basalts indicate that the chemical heterogeneity of mantle-derived rocks is inherited in part from their sources. Oceanic tholeiitic basalts show a tight correlation between the variances of Nd, Hf, Sr, and Pb isotopic ratios and the variances of respective radiogenic additions that could be accumulated in these rocks over a time period of 〈t〉 = 1.8 Gyr. This paradox clearly indicates that variations in all the mentioned isotopic systems in the mantle cannot be understood without the analysis of the geochemical heterogeneity of rocks.The close to lognormal distributions of lithophile trace elements in oceanic tholeiitic basalts and the character of correlations between them suggest that magmatic differentiation was the major mechanism of the formation of chemical heterogeneity in the mantle. The role of metasomatism in the global transport of trace elements and formation of the geochemically heterogeneous mantle is probably rather limited. Intrusive processes within the mantle could result in the development of chemical and, after a period of time, isotopic anomalies in the mantle. Simple calculations show that long-lived geochemical anomalies related to alkaline magmatism could be responsible for EM-I type isotopic anomalies, and geochemical anomalies produced in the mantle by enriched tholeiitic melts could be sources of EM-II type isotopic anomalies. The analysis of the distribution of the isotopic compositions of mantle-derived igneous rocks in various “isochron” coordinates suggested that the formation of geochemical anomalies in the mantle is a long-term process lasting for hundreds of millions of years. Nonetheless, trends approaching 4.5 Ga were never observed in such diagrams, i.e., the mantle is in general rejuvenated in all isotopic systems. Both on global and local scales, there are no mantle domains that have remained geochemically closed and isolated since the Earth’s formation. The entire mantle is involved in material exchange processes.The development of isotopic systems in the mantle was explored by means of statistical modeling accounting for the tendency of a continuous increase in the chemical heterogeneity of the mantle source and the tendency of obliteration of the isotopic heterogeneity owing to the convective mixing in the mantle. The modeling demonstrated that the character of the isotopic heterogeneity of the mantle is statistically consistent with the character of its chemical heterogeneity. The mantle isotopic anomalies HIMU, EM-I, and EM-II were generated by two simultaneous processes: the magmatic differentiation of mantle material and its not very efficient mixing.  相似文献   

8.
Subduction related basalts display wide ranges in large ion lithophile element ratios (e.g., Rb/Ba and Rb/ Sr) which are unlikely to result from mixing, but suggest a role for small degree partial melting of a relatively Rb-poor mantle wedge source. However, these variations do not correlate with other trace element criteria, such as the depletions of high field strength elements (HFSE) and light rare earth elements (LREE) relative to the LILE, which characterise subduction related magmatism. Integration of radiogenic isotope and trace element data demonstrates that the elemental enrichment cannot be simply related to two component mixtures inferred from isotopic variations. Thus a minimum of three components is required to describe the geochemistry of subduction zone basalts. Two are subduction related: high Sr/Nd material is derived from the dehydration of subducted basaltic ocean crust, and a low Sr/Nd component is thought to be from subducted terrigenous sediment. The third component is in the mantle wedge, it is usually similar to the source of MORB, particularly in its isotopic composition. However, in some cases, notably continental areas, more enriched mantle wedge material with relatively high 87Sr/86Sr, low 143Nd/144Nd and elevated incompatible trace element contents may be involved Mixing of these three components is capable of producing both the entire range of Sr, Nd and Pb isotope signatures observed in destructive margin basalts, and their distinctive trace element compositions. The isotope differences between Atlantic and Pacific island arc basalts are attributed to the isotope compositions of sediments in the two oceans.  相似文献   

9.
夏甸金矿是胶东金矿集区中一处大型焦家式矿床。文章在详尽的岩相学和矿相学研究基础上,对该矿床进一步开展 了H-O同位素并首次开展了He-Ar和Sr-Nd-Pb同位素示踪研究,为该矿床成矿流体及成矿物质来源提供了新的制约。石 英中流体包裹体的H-O同位素（δDV-SMOW=-102.3‰~-93.9‰,δ18OH2O=-0.2‰~1.6‰） 揭示出成矿流体主要为富集地幔流体, 并有少许大气降水加入;黄铁矿中He-Ar同位素[3He/4/He=0.58×10− 6~1.90×10− 6 （0.42~1.36 Ra）,40Ar/36Ar=724.7~1358.4]同样 表明成矿流体以富集地幔流体为主导;矿石及蚀变岩的Nd-Pb同位素既不同于围岩花岗岩,也不同于基底变质岩,与胶东 地区中生代软流圈地幔起源的玄武岩也相差甚远,而与胶东地区中生代富集岩石圈地幔起源的煌斑岩相一致,但它们的初 始87Sr/86Sr比值明显高于煌斑岩,甚至高于围岩花岗岩。Sr-Nd-Pb同位素特征表明成矿流体及成矿物质来源于富集岩石圈地 幔,并在其上升过程中与基底变质岩发生了相互作用。  相似文献   

10.
Based on detailed petrological, geochemical, and isotope-geochemical study, fragments of fresh pillow lavas with chilled glass margins dredged at the Sierra-Leone test site in the axial MAR rift zone between 5° and 7°N correspond to MORB tholeiites, which are not primitive mantle melts but were differentiated in intermediate magmatic (intrusive) chambers. Small-scale geochemical and Sr-Nd isotope heterogeneities were established for the first time in the basalts and their glasses. It was shown that some samples show significant nonsystematic differences in the 87Sr/86Sr ratio between the basalts and their chilled glasses and less significant difference in ?Nd; higher Sr ratios can be observed both in the glasses and basalts of the same lava fragments. No significant correlation is observed between the isotope characteristics of the samples and their geochemistry; it was also shown that seawater did not affect the Sr and Nd isotope composition of the chilled glasses of the studied pillow lavas. It is suggested that such differences in isotope ratios are related to a small-scale heterogeneity of the melts owing to incomplete homogenization during their rapid ascent to the surface. The heterogeneity of the basaltic melts is explained by their partial contamination by the older plutonic rocks (especially gabbroids) of the lower oceanic crust, through which they ascended to the ocean floor surface. The wider scatter of the Sr isotopic ratios relative to Nd is related to the presence of xenocrysts of calcic plagioclase; correspondingly, the absence of a Nd mineral carrier in the rocks results in less distinct Nd isotope variations. It was shown that all of the studied basalts define a single trend along the mantle correlation array in the Sr-Nd isotope diagram. The causes of this phenomenon remain unclear.  相似文献   

11.
夏甸金矿是胶东金矿集区中一处大型焦家式矿床。文章在详尽的岩相学和矿相学研究基础上，对该矿床进一步开展 了H-O同位素并首次开展了He-Ar和Sr-Nd-Pb同位素示踪研究，为该矿床成矿流体及成矿物质来源提供了新的制约。石 英中流体包裹体的H-O同位素（δDV-SMOW=-102.3‰~-93.9‰，δ18OH2O=-0.2‰~1.6‰） 揭示出成矿流体主要为富集地幔流体， 并有少许大气降水加入；黄铁矿中He-Ar同位素[3He/4/He=0.58×10− 6~1.90×10− 6 （0.42~1.36 Ra），40Ar/36Ar=724.7~1358.4]同样 表明成矿流体以富集地幔流体为主导；矿石及蚀变岩的Nd-Pb同位素既不同于围岩花岗岩，也不同于基底变质岩，与胶东 地区中生代软流圈地幔起源的玄武岩也相差甚远，而与胶东地区中生代富集岩石圈地幔起源的煌斑岩相一致，但它们的初 始87Sr/86Sr比值明显高于煌斑岩，甚至高于围岩花岗岩。Sr-Nd-Pb同位素特征表明成矿流体及成矿物质来源于富集岩石圈地 幔，并在其上升过程中与基底变质岩发生了相互作用。  相似文献   

12.
Mumbai City, situated on the western Indian coast, is well known for exposures of late-stage Deccan pillow basalts and spilites, pyroclastic rocks, rhyolite lavas, and trachyte intrusions. These rock units, and a little-studied sequence of tholeiitic flows and dykes in the eastern part of Mumbai City, constitute the west-dipping limb of a regional tectonic structure called the Panvel flexure. Here we present field, petrographic, major and trace element and Sr–Nd isotopic data on these tholeiitic flows and dykes, best exposed in the Ghatkopar–Powai area. The flows closely resemble the Mahabaleshwar Formation of the thick Western Ghats sequence to the east, in Sr–Nd isotopic ratios and multielement patterns, but have other geochemical characteristics (e.g., incompatible trace element ratios) unlike the Mahabaleshwar or any other Formation. The flows may have originated from a nearby eruptive center, possibly offshore of Mumbai. Two dykes resemble the Ambenali Formation of the Western Ghats in all geochemical characteristics, though they may not represent feeders of the Ambenali Formation lavas. Most dykes are distinct from any of the Western Ghats stratigraphic units. Some show partial (e.g., Sr–Nd isotopic) similarities to the Mahabaleshwar Formation, and these include several dykes with unusual, concave-downward REE patterns suggesting residual amphibole and thus a lithospheric source. The flows and dykes are inferred to have undergone little or no contamination, by lower continental crust. Most dykes are almost vertical, suggesting emplacement after the formation of the Panvel flexure, and indicate considerable east–west lithospheric extension during this late but magmatically vigorous stage of Deccan volcanism.  相似文献   

13.
罗迪柯  陈靖  姚仲友  匡福祥  姚春彦 《地质通报》2017,36(12):2197-2207
圭亚那地盾位于南美洲亚马孙克拉通的北部,其北部广泛发育太古宙典型的花岗岩-绿岩带,主要岩石组成为花岗岩、片麻岩和英云闪长岩,古元古代变质超基性-基性火山岩-侵入岩、其他变质火山岩等。由于独特的地质构造位置和复杂的构造演化历史,形成了良好的绿岩型金成矿地质背景,产生了大量的金矿床。通过总结圭亚那地盾北部绿岩带的岩石特征、成岩时代和构造演化历史,对委内瑞拉埃尔卡劳金矿、圭亚那欧迈金矿和苏里南罗瑟贝尔金矿进行典型矿床剖析,系统研究了该区绿岩带型金矿的成矿地质背景、成矿流体及成矿年代学特征,建立了区域绿岩带型金矿成矿模型,并在分析找矿要素的基础上,提出圭亚那地盾北部的金矿找矿方向。  相似文献   

14.
The Central African Copperbelt lies within the Lufilian orogenic belt, in the border region between the Democratic Republic of Congo (DRC) and Zambia. A Sr and Nd isotope study was performed on gangue carbonates associated with multiphase mineralisation at the Zambian Konkola and Nkana deposits. Comparison with isotopic signatures of basement rocks provides new insights into the likely metal source(s) for the Cu–Co mineralisation. At least three mineralisation phases can be identified with respect to the Lufilian orogeny. Gangue carbonates of the first, pre- to syn-kinematic mineralisation phase in both deposits have Sr and Nd isotopic compositions that correspond to felsic rocks of the Domes Region, a tectonic zone in the Zambian part of the Lufilian Belt where basement rocks crop out. However, the isotopic signatures from both deposits differ. This can be attributed to local variation in isotopic composition of the basement below the deposits. Radiogenic isotope ratios suggest that subsequent, syn-kinematic mineralisation at both sites occurred due to the remobilisation of precursor ore. Petrographic evidence indicates that the third, late-kinematic mineralisation phase at Nkana resulted from a renewed input of metals with a mafic affinity (e.g. Co, Ni). However, Sr and Nd isotope ratios resemble those of the earlier mineralisation phases and do not reflect a change in source composition. Nonetheless, comparison with the isotopic signatures of the Co-poor Konkola deposit and Co-rich stratiform deposits in the DRC might indicate a mafic component in the Nkana metal source. Calculated mixed isotopic compositions support such a mafic component.  相似文献   

15.
Rare-earth-element, radiogenic and oxygen isotope, and mineral chemical data are presented for tholeiitic and alkaline Quaternary volcanism from Karasu Valley (Hatay, southeastern Turkey). Karasu Valley is the northern segment of the Dead Sea transform fault and is filled with flood-basalt type volcanics of Quaternary age. This valley is an active fault zone that is known as “Karasu fault,” extending in a NE-SW direction. The Karasu Valley basaltic volcanics (KVBV) are subaphyric to porphyritic, with variable amounts of olivine, clinopyroxene, and plagioclase phenocrysts. Alkali basalts are generally characterized by high contents of olivine, clinopyroxene, and plagioclase phenocrysts. Their groundmass contains olivine, clinopyroxene, plagioclase, and Fe-Ti oxides. Tholeiitic basalts are subaphyric to porphyritic (high contents of olivine, clinopyroxene, and plagioclase). Their groundmass is similar to that of alkali basalts. The range of olivine phenocryst and microlite compositions for all analyzed samples is Fo81 to Fo43. Plagioclase compositions in both tholeiitic and alkali basalts range from andesine, An38 to bytownite, An72. Clinopyroxene compositions range from diopside to calcic augite. Most of the olivine, plagioclase, and clinopyroxene phenocrysts are normally zoned and/or unzoned. Fe-Ti oxides in both series are titanomagnetite and ilmenite.

Based on normative and geochemical data, the Karasu Valley basaltic volcanics are mostly olivine and quartz-tholeiites, and relatively lesser amount of alkali olivine-basalts. KVBV have low K2O/Na2O ratios, typically between 0.25 and 0.45. Olivine- and quartz-tholeiites are older than alkali olivine-basalts. Olivine tholeiites have Zr/Nb and Y/Nb ratios similar to alkaline rocks, but their Ba/Nb, Ba/La, and La/Nb ratios are slightly higher than alkali olivine-basalts. In contrast, quartz-tholeiites have the highest Ba/Nb, Ba/La, Zr/Nb, and Y/Nb and the lowest Nb/La ratios among the KVBV. Alkali basalts have 87Sr/86Sr and 143Nd/144Nd ratios ranging from 0.703353 to 0.704410 and 0.512860 to 0.512910, respectively. In contrast, quartz-tholeiites have higher 87Sr/86Sr and lower 143Nd/144Nd ratios, which vary from 0.704410 to 0.705490 and 0.512628 to 0.512640, respectively. Olivine tholeiites have intermediate isotopic compositions ranging from 0.703490 to 0.704780 and 0.512699 to 0.512780, respectively. 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb isotopic ratios of KVBV range from 18.817 to 19.325, 15.640 to 15.718, and 39.054 to 39.223, respectively. The range of O isotope values is between +5.84 and +7.97‰. The higher O and Sr isotopes in olivine- and quartz-tholeiites relative to alkali olivine-basalts can be explained by contamination of magmas by crustal materials.

The KVBV have intraplate chemistry similar to that of other tholeiitic and alkaline basalts in other within-plate environments, and isotopes range from isotopically depleted mantle to enriched isotope compositions similar to some enriched ocean islands. Trace-element and isotope data indicate that the KVBV are derived from a common OIB-like asthenospheric mantle source, but they have experienced different degrees of crustal contamination during their ascent to the surface, contemporaneous with little fractional crystallization. Although quartz-tholeiites display significant effects of crustal contamination, alkali olivine-basalts appear to have negligible or no crustal contamination in their geesis.  相似文献   

16.
Broken Hill ore deposition occurred during the highest geothermal gradient coeval with an event of bimodal basic-rhydacitic volcanism. The depositional environment is interpreted as an ensialic rift on the basis of the sedimentary facies, ferro- and low-K tholeiitic basalts, and bimodal basic-calc alkaline (rhyolite, rhyodacite) volcanism. The orebody is of unusual composition characterised by abundant carbonate, fluorite and fluorapatite, abundant LIL-, K- and Rb-rich premetamorphic alteration assemblages, primordial S and Pb isotopic values, Sr isotopes possibly indicating a heterogeneous source, S : Se in the magmatic range, and zoning suggestive of cooling of the ore fluid.It is suggested that in the mature stage of rifting, propagation of deep fractures suddenly devolatilized the mantle, released CO2 and other fluids which, together with basalts, ascended and caused crustal melting to form acid magmas. The resultant ore fluid exhalation and basaltic and rhyodacitic volcanism were therefore coeval. Rapid deposition of ore from a fluid of unusual composition in a basin or graben within the rift formed a deposit which is not too dissimilar in composition from a carbonatite.The composition of the associated basic rocks and younger alkaline rocks, the premetamorphic alteration assemblage, and the orebody chemistry all suggest that the Lower Proterozoic source area for the ore fluids was metasomatized mantle.  相似文献   

17.
行洛坑钨矿位于武夷山成矿带中部,是该带目前规模最大的钨矿床。钨矿体主要产于强烈蚀变的似斑状黑云母花岗岩岩株顶部,发育细脉浸染状、网脉状及大脉状多种矿化类型,黑钨矿与白钨矿含量近1∶1。关于矿床的流体演化过程与成矿机制目前仍不清楚,成因存在较大争议。本文在详细成矿阶段划分的基础上,对不同阶段产出的不同世代白钨矿开展了系统的原位LA-ICP-MS微量元素和Sr同位素、以及流体包裹体和H-O同位素的研究工作。行洛坑钨矿由早至晚可以划分为3个成矿阶段:细脉浸染状白钨矿-辉钼矿阶段(阶段Ⅰ)、钾长石-白钨矿-黑钨矿-绿柱石阶段(阶段Ⅱ)及硫化物-黑钨矿-白钨矿-碳酸盐阶段(阶段Ⅲ)。流体包裹体研究显示成矿流体为中高温、低盐度的Na Cl-H_2O-CO_2体系。H-O与Sr同位素表明成矿流体主要为岩浆流体,仅成矿晚期阶段有少量的大气降水加入。阶段I白钨矿相对富REE、Mo、Na和Nb,贫Sr;而随着流体演化,白钨矿REE、Mo、Na、Nb含量逐渐降低,Sr含量显著升高。阶段I白钨矿呈自形-半自形粒状,CL图像显示细密的、均匀的震荡环带,稀土元素主要与Na和Nb结合进入白钨矿晶格;阶段Ⅱ、阶段Ⅲ白钨矿呈半自形-他形,不发育或仅发育宽缓的、不规则震荡环带,稀土元素与Ca(Ca的离子空位)结合置换白钨矿中的Ca。结合蚀变与矿化特征,认为阶段I白钨矿形成于低水岩比环境,由初始岩浆流体沿微小裂隙渗透交代而形成;而阶段Ⅱ、Ⅲ白钨矿形成于高水岩比环境,CO_2的不混溶作用伴随强烈的水岩反应导致了钨的富集沉淀。结合矿床地质特征,认为行洛坑钨矿属于广义的斑岩型钨矿,细脉浸染状矿化构成了钨成矿的基础,而网脉状、大脉状矿化的叠加是钨进一步富集的关键。  相似文献   

18.
Jifeng Ying  Xinhua Zhou  Hongfu Zhang 《Lithos》2004,75(3-4):413-426
Major and trace element and Nd–Sr isotope data of the Mesozoic Laiwu–Zibo carbonatites (LZCs) from western Shandong Province, China, provide clues to the petrogenesis and the nature of their mantle source. The Laiwu–Zibo carbonatites can be petrologically classified as calcio-, magnesio- and ferro-carbonatites. All these carbonatites show a similarity in geochemistry. On the one hand, they are extremely enriched in Ba, Sr and LREE and markedly low in K, Rb and Ti, which are similar to those global carbonatites, on the other hand, they have extremely high initial 87Sr/86Sr (0.7095–0.7106) and very low Nd (−18.2 to −14.3), a character completely different from those global carbonatites. The small variations in Sr and Nd isotopic ratios suggest that crustal contamination can not modify the primary isotopic compositions of LZC magmas and those values are representatives of their mantle source. The Nd–Sr isotopic compositions of LZCs and their similarity to those of Mesozoic Fangcheng basalts imply that they derived from an enriched lithospheric mantle. The formation of such enriched lithospheric mantle is connected with the major collision between the North China Craton (NCC) and the Yangtze Craton. Crustal materials from the Yangtze Craton were subducted beneath the NCC and melts derived from the subducted crust of the Yangtze Craton produced an enriched Mesozoic mantle, which is the source for the LZCs and Fangcheng basalts. The absence of alkaline silicate rocks, which are usually associated with carbonatites suggest that the LZCs originated from the mantle by directly partial melting.  相似文献   

19.
The Rhön area as part of the Central European Volcanic Province (CEVP) hosts an unusual suite of Tertiary 24-Ma old hornblende-bearing alkaline basalts that provide insights into melting and fractionation processes within the lithospheric mantle. These chemically primitive to slightly evolved and isotopically (Sr, Nd, Pb) depleted basalts have slightly lower Hf isotopic compositions than respective other CEVP basalts and Os isotope compositions more radiogenic than commonly observed for continental intraplate alkaline basalts. These highly radiogenic initial 187Os/188Os ratios (0.268–0.892) together with their respective Sr–Nd–Pb isotopic compositions are unlikely to result from crustal contamination alone, although a lack of Os data for lower crustal rocks from the area and limited data for CEVP basalts or mantle xenoliths preclude a detailed evaluation. Similarly, melting of the same metasomatized subcontinental lithospheric mantle as inferred for other CEVP basalts alone is also unlikely, based on only moderately radiogenic Os isotope compositions obtained for upper mantle xenoliths from elsewhere in the province. Another explanation for the combined Nd, Sr and Os isotope data is that the lavas gained their highly radiogenic Os isotope composition through a mantle “hybridization”, metasomatism process. This model involves a mafic lithospheric component, such as an intrusion of a sublithospheric primary alkaline melt or a melt derived from subducted oceanic material, sometime in the past into the lithospheric mantle where it metasomatized the ambient mantle. Later at 24 Ma, thermal perturbations during rifting forced the isotopically evolved parts of the mantle together with the peridotitic ambient mantle to melt. This yielded a package of melts with highly correlated Re/Os ratios and radiogenic Os isotope compositions. Subsequent movement through the crust may have further altered the Os isotope composition although this effect is probably minor for the majority of the samples based on radiogenic Nd and unradiogenic Sr isotope composition of the lavas. If the radiogenic Os isotope composition can be explained by a mantle-hybridization and metasomatism model, the isotopic compositions of the hornblende basalts can be satisfied by ca. 5–25% addition of the mafic lithospheric component to an asthenospheric alkaline magma. Although a lack of isotope data for all required endmembers make this model somewhat speculative, the results show that the Re–Os isotope system in continental basalts is able to distinguish between crustal contamination and derivation of continental alkaline lavas from isotopically evolved peridotitic lithosphere that was contaminated by mafic material in the past and later remelted during rifting. The Hf isotopic compositions are slightly less radiogenic than in other alkaline basalts from the province and indicate the derivation of the lavas from low Lu–Hf parts of the lithospheric mantle. The new Os and Hf isotope data constrain a new light of the nature of such metasomatizing agents, at least for these particular rocks, which represent within the particular volcanic complex the first product of the volcanism.  相似文献   

20.
Strontium, Nd, Pb, Hf, Os, and O isotope compositions for 30 Quaternary lava flows from the Mount Adams stratovolcano and its basaltic periphery in the Cascade arc, southern Washington, USA indicate a major component from intraplate mantle sources, a relatively small subduction component, and interaction with young mafic crust at depth. Major- and trace-element patterns for Mount Adams lavas are distinct from the rear-arc Simcoe volcanic field and other nearby volcanic centers in the Cascade arc such as Mount St. Helens. Radiogenic isotope (Sr, Nd, Pb, and Hf) compositions do not correlate with geochemical indicators of slab-fluids such as (Sr/P) n and Ba/Nb. Mass-balance modeling calculations, coupled with trace-element and isotopic data, indicate that although the mantle source for the calc-alkaline Adams basalts has been modified with a fluid derived from subducted sediment, the extent of modification is significantly less than what is documented in the southern Cascades. The isotopic and trace-element compositions of most Mount Adams lavas require the presence of enriched and depleted mantle sources, and based on volume-weighted chemical and isotopic compositions for Mount Adams lavas through time, an intraplate mantle source contributed the major magmatic mass of the system. Generation of basaltic andesites to dacites at Mount Adams occurred by assimilation and fractional crystallization in the lower crust, but wholesale crustal melting did not occur. Most lavas have Tb/Yb ratios that are significantly higher than those of MORB, which is consistent with partial melting of the mantle in the presence of residual garnet. δ 18O values for olivine phenocrysts in Mount Adams lavas are within the range of typical upper mantle peridotites, precluding involvement of upper crustal sedimentary material or accreted terrane during magma ascent. The restricted Nd and Hf isotope compositions of Mount Adams lavas indicate that these isotope systems are insensitive to crustal interaction in this juvenile arc, in stark contrast to Os isotopes, which are highly sensitive to interaction with young, mafic material in the lower crust.  相似文献   

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