Trace element and isotopic variations in a zoned pluton and associated volcanic rocks,Unalaska Island,Alaska: A model for fractionation in the Aleutian calcalkaline suite

Trace elements, including rare earth elements (REE), exhibit systematic variations in plutonic rocks from the Captains Bay pluton which is zoned from a narrow gabbroic rim to a core of quartz monzodiorite and granodiorite. The chemical variations parallel those in the associated Aleutian calcalkaline volcanic suite. Concentrations of Rb, Y, Zr and Ba increase as Sr and Ti decrease with progressive differentiation. Intermediate plutonic rocks are slightly enriched in light REE (La/Yb=3.45–9.22), and show increasing light REE fractionation and negative Eu anomalies (Eu/Eu^*=1.03–0.584). Two border-zone gabbros have similar REE patterns but are relatively depleted in total REE and have positive Eu anomalies; indicative of their cumulate nature. Initial ⁸⁷Sr/⁸⁶Sr ratios in 8 samples (0.70299 to 0.70377) are comparable to those of volcanic rocks throughout the arc and suggest a mantle source for the magmas. Oxygen isotopic ratios indicate that many of the intermediate plutonic rocks have undergone oxygen isotopic exchange with large volumes of meteoric water during the late stages of crystallization; however no trace element or Sr isotopic alteration is evident.Major and trace element variations are consistent with a model of inward fractional crystallization of a parental high-alumina basaltic magma at low pressures (6 kb). Least-squares approximations and trace element fractionation calculations suggest that differentiation in the plutonic suite was initially controlled by the removal of calcic plagioclase, lesser pyroxene, olivine and Fe-Ti oxides but that with increasing differentiation and water fugacity the removal of sub-equal amounts of sodic plagioclase and hornblende with lesser Fe-Ti oxides effectively drove residual liquids toward dacitic compositions. Major and trace element compositions of aplites which intrude the pluton are not adequately explained by fractional crystallization. They may represent partial melts derived from the island arc crust. Similarities in Sr isotopes, chemical compositions and differentiation trends between the plutonic series and some Aleutian volcanic suites indicates that shallow-level fractional crystallization is a viable mechanism for generating the Aleutian calcalkaline rock series.LDGO Contribution no. 2964     

Geochemistry of tholeiites from Lanai,Hawaii

Lanai is the third smallest of the fifteen principal subaerial shield volcanoes of the Hawaiian hotspot. This volcano apparently became extinct during the shield-building stage of volcanism, as shown by the absence of both alkalic cap and post-erosional lavas. Major and trace element analyses of 22 new samples collected primarily from 3 stratigraphic sections show that Lanai tholeiites span a large range in composition. Some Lanai lavas are unique geochemically among Hawaiian tholeiites in having the lowest abundances of incompatible trace elements of any Hawaiian lavas and well-developed positive Eu anomalies. The geochemical characteristics of these low-abundance Lanai tholeiites are not the result of alteration, differences in mantle source modal mineralogy, the presence of residual accessory mantle phases or fractional crystallization of such phases, assimilation of depleted [MORB] wall-rock, or accumulation/resorption of phenocrysts or xenocrysts. Incompatible trace element ratios (e.g., Nb/La, Nb/Th, La/Th, La/Hf, Ce/Pb) in Lanai tholeiites span considerable ranges and form coherent trends with each other and with absolute abundances of these elements. Large variations in La/Sm, La/Yb, and absolute REE abundances at constant MgO suggest that Lanai tholeiites formed by variable amounts of partial melting. However, large ranges in incompatible element ratios cannot be explained solely by variations in partial melting of a geochemically homogeneous source, but must reflect geochemical heterogeneities in the Lanai source. Partial melting modeling indicates that the mixed Lanai source is probably LREE-enriched [i.e., (La/Yb)_CN>1]. One component in the Lanai source, exemplified by the low-abundance tholeiites, has markedly lower REE/HFSE, Th/HFSE, alkali/HFSE, and Ce/Pb ratios than other Lanai or Hawaiian tholeiites and may indicate the presence of recycled residual subduction zone materials in the Hawaiian plume source. The positive Eu anomalies that characterize the low-abundance Lanai tholeiites are not the result of plagioclase accumulation or assimilation but are a feature of this source component. Progressive temporal geochemical variations in Lanai tholeiites from 2 stratigraphic sections indicate that the source composition of these lavas probably evolved over time. This change could have resulted from a progressive decrease in the extent of partial melting of the Lanai source. The compositional variability of Lanai tholeiites suggests that geochemical heterogeneities in their source are larger than the scale of partial melting. Lanai tholeiites could not have formed by smaller degrees of partial melting of plume material than did the larger-volume Hawaiian shields. Therefore, volume differences between Hawaiian shields must be controlled primarily by differences in the volume of supplied plume material rather than by differences in the degree of partial melting. The premature cessation of eruptive activity at Lanai may be attributed to relatively large degrees of partial melting of a small plume.     

Young bimodal volcanism at Medicine Lake volcanic center,northern California

The last 10,000 years of activity at the Medicine Lake volcanic center in northern California is characterized by bimodal mafic and siliceous volcanism. Interflow element variations are complex and exhibit a discontinuity for most elements between 57 and 62 per cent SiO₂. No simple linear or curvilinear element trends exist between the mafic (Modoc) and siliceous (glass) volcanics.The geochemical variation patterns exhibited by volcanic rocks from the Medicine Lake volcanic center preclude any simple model for magma origin involving either varying degrees of melting or of fractional crystallization. A model is tentatively invoked for the andesites and basalts involving ? 35 per cent melting of eclogite (of altered rise tholeiite composition) in a descending slab followed by varying amounts of fractional crystallization and perhaps magma mixing. Up to 20 per cent of shallow fractional crystallization of plagioclase and minor Ti-magnetite seems to be required by the Sr, Eu anomaly, and TiO₂ distributions.Compositional variation and high δO¹⁸ values in most dacite glass flows are best interpreted in terms of a crustal origin involving up to 50 per cent partial melting of average continental crust. Rhyolite glasses may have formed by small degrees of melting (20–30 per cent) of this crust followed by 5–10 per cent of shallow fractional crystallization (removing dominantly plagioclase) or by 40–50 per cent fractional crystallization of a dacite parent (~63 per cent SiO₂) produced in the crust. The shallow fractional crystallization is necessary to explain the low Sr contents and large negative Eu anomalies in the rhyolites. Dacites from the Composite Flow are tentatively interpreted to have formed by shallow mixing of a hybrid magma (composed of varying amounts of andesite and dacite) with rhyolite prior to and during eruption.     

Dokhan volcanics of Gabal Monqul area,North Eastern Desert,Egypt: geochemistry and petrogenesis

The Dokhan volcanics are represented by a thick stratified lava flows succession of basalt, andesite, imperial porphyry, dacite, rhyodacite, rhyolite, ignimbrites, and tuffs. These lavas are interbanded with their pyroclastics in some places including banded ash flow tuffs, lithic tuffs, crystal lapilli tuffs, and agglomerates. They are typical calc–alkaline and developed within volcanic arc environment. All rocks show moderate enrichment of most large ion lithophile elements relative to high field strength elements (HFSE). The incompatible trace elements increase from basalt through andesite to rhyolite. The felsic volcanics are characterized by moderate total rare earth elements (REE) contents (162 to 392 ppm), less fractionated patterns {(Ce/Yb)_N = (1.24 to 10.93)}, and large negative Eu anomaly {(Eu/Eu*) = (0.15 to 0.92)}. The mafic volcanics have the lowest REE contents (61 to 192 ppm) and are relatively steep {(Ce/Yb)_N = (3.2 to 8.5)}, with no negative Eu anomalies {(Eu/Eu*) = (0.88 to 1)}. The rhyolite displays larger negative Eu anomaly (Eu/Eu* = 0.28) than those of other varieties, indicating that the plagioclase was an early major fractionating phase. The mineralogical and chemical variations within volcanics are consistent with their evolution by fractional crystallization of plagioclase and clinopyroxene.     

Case studies on the origin of basalt

The simplified model of basalt genesis described in Part I of this series, equilibrium partial melting followed by Rayleigh-type fractional crystallization, is applied to a stratigraphically controlled sequence of basalt flows from Kohala volcano. Major-element compositions were determined for 52 samples and show a time-stratigraphic progression from tholeiites through transitional basalts to alkali basalts. Twenty-six of these samples were analyzed by isotope dilution for K, Rb, Cs, Sr, Ba and the REE, 13 for⁸⁷Sr/⁸⁶Sr, and 19 for Co, Cr, Ni and V by atomic absorption. After a simple, first-order correction for the effects of fractional crystallization (involving mostly olivine and aluminous clinopyroxene), the major element concentrations cluster tightly, and the incompatible trace elements show monotonic increases in concentration as a function of stratigraphic height. The process identification plot shows that all the (fractionation corrected) melt compositions can be explained by equilibrium partial melting of compositionally identical batches of source material. The REE and Sr are fractionated because of the presence of residual clinopyroxene. Garnet may also be present but in much smaller amounts. In this respect our results differ significantly from those of Leeman et al. (1980). The calculated chondrite-normalized REE patterns of the source are nearly flat to slightly convex upward. Therefore there is no need to invoke special mechanisms, such as metasomatic REE preenrichment of the source, in order to explain the petrogenesis of the suite of lavas. Specifically, Ce concentrations ranging from 20 to 250 times chondritic are all explained by the same calculated source pattern having a chondrite-normalized ratio of Ce/Sm=0.9±0.2. However, the normalized ratio Ce/Ba?2 shows that the source is not simply primitive mantle.     

新疆克拉玛依百口泉蛇绿混杂岩中辉长岩岩石学和地球化学研究

克拉玛依蛇绿混杂岩带百口泉剖面由尖晶石蛇纹岩、辉长岩、玄武岩和硅质岩组成。岩相学研究表明,百口泉辉长岩分为堆晶岩(具堆晶结构)和辉长岩(具辉长结构)两类,且均经历了低-中级变质改造。微量元素地球化学显示其岩浆起源于亏损地幔,强烈的Sr异常和Eu异常表明强烈的斜长石堆晶过程。根据其稀土配分模式推测其源区为尖晶石相的地幔橄榄岩。结合野外地质关系和地球化学特征,白碱滩尖晶石二辉橄榄岩能够代表其源区成分,利用微量元素模拟其岩浆演化过程显示:尖晶石二辉橄榄岩发生2.5%部分熔融所形成的熔体,通过10%～20%分离结晶可以形成堆晶辉长岩,经过80%～90%分离结晶则可以形成具辉长结构的辉长岩。因此,蛇绿混杂岩中零星分布的堆晶岩和辉长岩团块是同源岩浆演化的产物。对分离结晶过程中Nb元素地球化学行为的研究表明,岩浆的结晶分异能够导致辉长岩明显亏损Nb。     

Rare earth element distribution in lavas and ultramafic xenoliths from the Comores Archipelago,Western Indian Ocean

Lavas and included xenoliths from the Comores Archipelago have been analysed for the rare earth elements (REE) La-Lu. Among basaltic lava types fractionation of REE rock/chondrite distribution patterns is more extreme with greater SiO₂ undersaturation and contents of incompatible elements. Enrichment and slight fractionation of REE in the rock series basanite-phonolite is considered compatible with a model of fractional crystallisation at low pressures involving mainly olivine and clinopyroxene, and to a much lesser extent, plagioclase. Apatite is probably effective in curtailing further enrichment of REE. High level fractional crystallisation and eclogite fractionation at depth appear unlikely causes for the relative enrichment of light REE (La-Eu) in the undersaturated basalts. This effect is more probably due to mineralogical control during partial melting in the upper mantle. Lherzolite xenoliths are poor in REE, exhibiting a slight relative depletion in the light REE. These patterns are interpreted as those of possible mantle material subjected to small degrees of partial melting, although not necessarily related to those melts erupted as lava flows at the surface.     

Rare earth element concentrations in a suite of basanitoids and alkali olivine basalts from Grenada,Lesser Antilles

A suite of basanitoids and alkali olivine basalts from Grenada, Lesser Antilles were analyzed for rare earth elements. The REE concentrations of these rocks are characterized by a small variation in the heavy REE (7 to 9 times chondrite) and a large variation in the light REE (17 to 93 times chondrite). Among the possible mechanisms to account for the REE variations, fractional crystallization processes at low and high pressures, and partial melting processes (both batch melting and fractional melting) were examined, using the partition relationships of REE among silicate minerals and melts. It is suggested that the observed REE variations are best explained by variable degrees of batch partial melting, in which garnet is present as one of the solid phases through 2 to 17% melting of a garnet lherzolite parent rock.     

藏北羌塘中西部红脊山地区早二叠世埃达克质岩石的发现及其地质意义

近期在羌塘中西部红脊山地区一套二叠纪蛇绿岩中首次发现了埃达克质岩石,呈脉状侵入到蛇绿岩中。对该套岩石进行了详细的岩石学、锆石U-Pb年龄和地球化学研究,重点讨论岩石成因及地质意义。埃达克质岩石岩性为白云母花岗岩,岩石中锆石晶形较完整,具典型的岩浆生长环带,结合Th/U值(0.22~0.63),表明其为典型的岩浆锆石。锆石LA-ICP-MS定年结果为271.7Ma±2.3Ma,表明其形成时代为早二叠世。岩石具有较高的Si O2、Al2O3含量和较低的K2O/Na2O值,为弱过铝质岩石。稀土元素配分模式呈右倾的曲线,重稀土元素分馏中等,Eu异常变化较小;微量元素Y、Yb含量较低,Sr含量中等,在微量元素蛛网图上表现出Rb、U、K正异常和Nb、Ta、P、Ti负异常。这与俯冲洋壳熔融形成的埃达克质岩石特征相似。红脊山埃达克质岩石是俯冲的古特提斯洋在角闪岩相—榴辉岩相条件下部分熔融形成的,残留相主要为石榴子石+角闪石。较早产生的熔体与地幔橄榄岩充分发生交代作用,后产生的熔体与地幔橄榄岩交代作用较弱,向上运移过程中斜长石发生分离结晶。红脊山埃达克质岩石的发现,表明古特提斯洋在早二叠世开始俯冲消减,大洋进入消退阶段。     

Geochemistry and origin of massif-type anorthosites

Samples of Proterozoic anorthosite complexes from the Adirondack Mountains of New York, Burwash Area of Ontario, and the Nain Complex of Labrador, ranging in composition from anorthosite to anorthositic gabbro, have been analyzed for major elements, Rb, Sr, Ba and nine rare-earth elements (REE), in order to set limits on the compositions and origins of their parent magmas. Similar rock types from the different areas have similar major and trace element compositions. The anorthosites have high Sr/Ba ratios, low REE abundances (Ce about 10, Yb about 0.5–1.5 times chondrites) and large positive Eu anomalies. The associated anorthositic gabbros have lower Sr/Ba ratios, REE abundances nearly an order of magnitude higher than the anorthosites, and small to negligible positive Eu anomalies.Model calculations using the adcumulate rocks with the lowest REE abundances and published distribution coefficients yield parent liquids having REE abundances and patterns similar to those of the associated anorthositic gabbros with the highest REE abundances. Rocks with intermediate REE abundances are the result of incorporation of a liquid component by a plagioclase-rich cumulate similar to the adcumulate samples. The analytical data and model calculations both suggest parent liquids having compositions of 50–54% SiO₂, greater than 20% Al₂O₃, about 1% K₂O, atomic Mg/(Mg+Fe²⁺) ratios (Mg No.'s) of less than 0.4, 15–30 ppm Rb, 400–600 ppm Sr and 400–600 ppm Ba, 40–50 times chondrites for Ce and 8–10 times chondrites for Yb.The low atomic Mg/(Mg+Fe²⁺) values for these rocks combined with geophysical evidence suggesting there are not large quantities of ferromagnesian material at depth, indicate that the anorthositic masses are not products of fractional crystallization of mafic melt derived from melting of the mantle. Rather, it is suggested that they are a result of partial melting of tholeiitic compositions at depths shallower than the basalt-eclogite transformation, leaving a pyroxene-dominated residue.     

哈拉达拉辉长岩以及其中磁铁矿-辉石脉的岩石学和地球化学研究

西南天山哈拉达拉杂岩体主要由橄长岩、橄榄辉长岩和辉长岩组成,岩浆通过早期橄榄石和斜长石结晶分离后,残余岩浆侵位形成了辉长岩.辉长岩中单斜辉石(Cpx-Ⅰ)的稀土元素含量低(REE ＜51 × 10-6),Eu负异常不明显,其他微量元素(如Sc、Cr)的含量和Mg#值(80～ 95)变化大(透辉石-普通辉石).磁铁矿-辉石脉穿切辉长岩,其中单斜辉石(Cpx-Ⅱ)的成分比较均一(透辉石).与Cpx-Ⅰ相比,Cpx-Ⅱ的稀土元素含量明显高(REE＞ 100× 10-6),且Eu负异常非常显著.与晚期富Fe基性岩浆的快速侵位不同,辉长岩的形成经历了复杂的演化过程.Cpx-Ⅰ和Cpx-Ⅱ均发育出溶结构,表明晚期富Fe基性岩浆快速侵位形成磁铁矿-辉石脉之后,哈拉达拉岩体或者经历了快速抬升(或者快速降温)的过程.岩浆过程结束后,低温热演活动形成了含金方解石-磁铁矿脉.研究这种热液脉,对本地区开展金矿找矿勘探有重要意义.     

Origin of ureilites inferred from a SIMS oxygen isotopic and trace element study of clasts in the Dar al Gani 319 polymict ureilite

Secondary ion mass spectrometer (SIMS) oxygen isotope analyses were performed on 24 clasts, representing 9 clast types, in the Dar al Gani (DaG) 319 polymict ureilite with precisions better than 1‰. Olivine-rich clasts with typical ureilitic textures and mineral compositions have oxygen isotopic compositions that are identical to those of the monomict ureilites and plot along the CCAM (Carbonaceous Chondrite Anhydrous Mineral) line. Other igneous clasts, including plagioclase-bearing clasts, also plot along the CCAM line, indicating that they were derived from the ureilite parent body (UPB). Thus, we suggest that some of the plagioclase-bearing clasts in the polymict ureilites represent the “missing basaltic component” produced by partial melting on the UPB.Trace element concentrations (Mg, K, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Rb, Sr and Ba) in ureilitic plagioclase and glass from 13 clasts were obtained by using the SIMS high mass resolution method. The trace element contents of the plagioclase generally show monotonic variations with anorthite content (mol%) that are consistent with partial melting and fractional crystallization. Incompatible trace element concentrations (K, Ti, and Ba) are low and variable for plagioclase with An > 40, indicating that the parental magmas for some clasts were derived from a depleted source. We performed partial melt modeling for CI and CM precursor compositions and compared the results to the observed trace element (K, Ba, and Sr) abundances in the plagioclase. Our results indicate that (1) the UPB evolved from a alkali-rich carbonaceous chondritic precursor, (2) parent melts of porphyritic clasts could have formed by 5-20% equilibrium partial melting and subsequent fractional crystallization, and (3) parent melts of the incompatible trace element-depleted clasts could be derived from fractional melting, where low degree (<10%) partial melts were repeatedly extracted from their solid sources.Thus, both the oxygen isotopic and trace element compositions of the plagioclase bearing clasts in DaG-319 suggest that the UPB underwent localized low degree-partial melting events. The partial melts could have been repeatedly extracted from the precursor, resulting in the formation of the olivine-pigeonite monomict ureilites as the final residue.     

The Role of Partial Melting and Fractional Crystallization in Determining Discordant Migmatite Leucosome Compositions

Anatectic migmatite leucosomes in the Quetico MetasedimentaryBelt (Superior Province) are discordant to the host rock layering.Two morphological varieties within the anatectic leucosome suiteare distinguished. The first type show little compositionalor textural variation either across, or along, the leucosomes.In contrast, the second variety exhibits both compositionaland textural variations in a single leucosome, typically withinternal cross-cutting relationships. Major-oxide contents varycomparatively little in the Quetico anatectic leucosome suite,but there is a considerable range in the incompatible element(REE, Hf, Zr, Y and Th) concentrations. In particular La contentsrange from 1.8 to 78.1 p.p.m. and the La/Yb ratios from 9.1to 101.9. Samples with high REE contents have negative Eu anomalies,whereas those with low total REE abundances have positive Euanomalies, which indicate that feldspar fractionation was importantin their petrogenesis. Three samples which have no Eu anomalies,and which are taken not to have experienced significant feldsparfractionation, are regarded as the closest approximation toa primary melt composition. Petrographic evidence indicates that only the most aluminousbulk compositions in the host rocks have melted, with cordieriteand biotite as the principal residual phases. Batch partialmelting models indicate that the three leucosomes without Euanomalies could have been derived from 40–80 per centpartial melting of the aluminous metasediments, but garnet musthave been a residual phase. Since the residuum from 40 per centpartial melting is more mafic than any of the rocks currentlyexposed in the area, it is concluded that the melting whichgave rise to the leucosomes occurred at greater depth. Crystallization models indicate that the observed range of leucosomecompositions can be derived by crystal fractionation of meltcompositions similar to the three leucosomes lacking Eu anomalies(i.e. the assumed primary melts). Samples with high abundancesof incompatible elements and negative Eu anomalies representfractionated melts, whereas those with low levels of REE andpositive Eu anomalies represent cumulates. Leucosome composition,morphology and texture can be related to crystallization history,notably the timing of crystallization with respect to leucosomeintrusion. In particular, those leucosomes that exhibit compositionaland textural zoning are interpreted to have undergone crystalfractionation during intrusion. Although a suite of migmatite leucosomes may be derived by partialmelting, it is concluded that the trace-element compositionof any particular leucosome depends, to a great extent, uponits segregation and crystallization history. Indeed, the primarymelt composition may not be preserved.     

Late Ediacaran post-collisional A-type syenites with shoshonitic affinities,northern Arabian-Nubian Shield: a possible mantle-derived A-type magma

The Abu Rumeil syenitic rocks represent the inner ring dyke of the Katherina Ring complex, southern Sinai, Egypt. They are divided petrologically into two types, alkali feldspar syenite and quartz syenite. The mineralogy and geochemistry of the syenites indicate an alkaline nature with a shoshonitic affinity. Although rare mafic xenocrysts overgrown by primary K-feldspars and overlapping rare earth element (REE) patterns indicate some role for crustal contamination, the trace element chemistry shows a dominant mantle contribution. The geochronology and field relations imply that the Abu Rumeil syenites were emplaced in a post-collisional, within-plate tectonic setting, yet they express the enrichments in large-ion lithophile elements relative to high field strength elements generally characteristic of subduction influence. We suggest that this signature is inherited from partial melting of a lithospheric mantle source previously affected by subduction during assembly of the Arabian-Nubian Shield. Little evidence of the early evolution of the suite is preserved; there are no associated mafic rocks. We therefore restrict our attention to a petrogenetic model that can explain the relations among the observed felsic composition. The REE patterns of all samples are enriched in light REE and fractionated, but it is notable that there are small positive Eu anomalies in the alkali-feldspar syenites contrasting with small negative Eu anomalies in the quartz syenites. Positive Eu anomalies suggest a cumulate nature for the alkali-feldspar syenites; there are also breaks in the slopes of most variation trends between the alkali-feldspar syenites and the quartz syenites. The general trends in all major oxides and trace elements within the suite can be modeled by fractional crystallization of feldspars—with smaller roles for pyroxene, biotite, apatite, and Fe-Ti oxides—from an intermediate liquid to form the quartz syenites and by assimilation of the near-liquidus phases into the same starting liquid to form the alkali feldspar syenites. The geothermobarometry of pyroxenes and amphiboles suggests shallow emplacement (<10 km depth) and crystallization temperatures ranging from 1100 °C down to 800 °C.     

Neoproterozoic magmatism in NW Sinai,Egypt: magma source and evolution of collision-related intracrustal anatectic leucogranite

The present study deals with tectonomagmatic evolution of the collision-related leucogranite located near the northwest corner of exposed basement in Sinai, Egypt. The area is composed of: (1) a gabbroic complex; (2) amphibolite; (3) post-orogenic leucogranite; (4) Feiran gneisses. The amphibolite and gabbroic suites, generated in an island arc environment, have a high Fe-tholeiitic affinity and were derived from two independent magmas. On the basis of rare earth element (REE) patterns, the gabbroic melts could have been generated from a garnet- and amphibole-bearing, enriched mantle, and were subsequently modified by fractional crystallization of pyroxene and amphibole with minor plagioclase, whereas the amphibolite melts could be derived from garnet-free depleted mantle.The leucogranite has high Al₂O₃ content (>13 wt%), alumina saturation index (ASI) mostly >1, and normative corundum, indicating a peraluminous nature. Chondrite-normalized REE patterns for the leucogranite show light REE enrichment (La/Sm_N=2.7–4.86), general flattening of the heavy REE (Gd/Lu_N=1.2–2), and negative europium (Eu) anomalies (Eu/Eu*=0.24–0.47). The peraluminous nature and enrichment of the incompatible elements (K, Rb, Ba and Th) in the leucogranite strongly suggest derivation from a crustal source. The most probable source for the leucogranite magmas is represented by the adjacent Feiran gneisses, which could have generated the leucogranite by dehydration melting under water-undersaturated conditions. It appears likely that the restite unmixing model is responsible for the chemical variations within the leucogranite. In accordance with this model, the chemical variation of the leucogranite can be attributed to varying degrees of separation of restitic material from the melt during its emplacement and solidification and fractional crystallization could have played a minor role during magma ascent through the crust.     

Abundance and distribution of the rare-earth elements and yttrium in the rocks and minerals of the Oka carbonatite complex,Quebec

are-earth (REE) and yttrium abundances were determined, by an ion-exchange-X-ray fluorescence procedure, for whole-rock (14) and mineral (87) samples from the Oka carbonatite complex. Whole-rock and mineral data indicate a trend of total REE + Y enrichment, and relative enrichment in light REE, in the order: ultrafenites < ijolites < okaites. The sövites may show wide variations in total REE + Y concentrations, but relative REE abundance patterns will be similar. The greatest REE and Y concentrations occur in apatite, niocalite, perovskite and pyrochlore. Many of the minerals show europium anomalies (both positive and negative), and these are believed to be the result of closed system competition between the various minerals for divalent Eu. The partition coefficients for mineral pairs are quite variable, indicating that the Oka rocks were emplaced through a wide-range of physicochemical and/or nonequilibrium conditions. A reasonable model for the origin of the complex involves a limited partial melting of mantle material, emplacement of the melt in a magma chamber, crystallization of mafic minerals resulting in a residual liquid which produced ijolite and subsequently okaite, and crystallization of the carbonatites from a volatile-rich, possibly immiscible, phase.     

云南龙陵地区苏帕河花岗岩形成时代与地球化学特征:泛非运动的岩浆响应

泛非期中酸性岩浆事件影响的时间和空间是国内外地质学家用来确定冈瓦纳范围的重要依据和重要标志之一,也是泛非运动在青藏高原的重要表现形式,发育于云南龙陵地区的苏帕河花岗岩就是其中的酸性岩之一.产于龙陵-瑞丽断裂(简称龙瑞断裂)南东侧的苏帕河花岗岩,其主体岩性为花岗闪长岩、二长花岗岩,岩体除了发育一系列北东向狭窄的片理化带之...     

Trace Element Geochemical Effects of Integrated Melt Extraction and 'Shaped' Melting Regimes

The mixing (integration) of liquids obtained as different massfractions of partial melting from source material of the samebulk composition, travelling along different mantle flow-linesthrough a melting regime, can result in deficiencies in therelative concentrations of those incompatible elements whosebulk distribution coefficients are numerically approximatelyequal to the average mass fraction of melt extracted from thetotal source material involved in the provision of the mixedmelts. These deficiencies can be very substantial, exceeding50% of the concentration which would have been expected to bepresent in the liquid if that same average mass fraction ofmelt had been extracted from the whole melting regime by simpleequilibrium or accumulated perfect fractional partial melting.The size of the deficit varies with the shape and plan-formof the melting region, and can be greatly reduced by subsequentperfect fractional crystallization of that liquid. Discriminationis increased between all elements whose distribution coefficientsare numerically smaller than the average mass fraction of partialmelt extracted from the whole region. These effects can leadto steepening of chondrite-normalized REE patterns and to apparentselective light rare earth enrichment in liquid and source. KEY WORDS: melt integration; shaped melting regimes; trace elements; numerical modelling     

西藏芒康盆地新生代高钾火山岩的主元素和同位素地球化学研究

元素和Pb-Sr-Nd同位素地球化学示踪结果表明,西藏芒康盆地内拉屋乡组高钾火山岩是在转换压缩引起的陆内俯冲背景下产生的,其可能源区为EMII型富集地幔端元。高场强元素Nb和Ta出现明显的负异常,表明在该火山岩源区内有陆壳物质的加入。稀土元素模拟结果显示岩浆源区成岩过程中有单斜辉石、斜长石和石榴子石的分离结晶。     

Geochemistry of the Chakradharpur granite—Gneiss complex—A Precambrian trondhjemite body from West Singhbhum,Eastern India

The Chakradharpur Granite—Gneiss complex (CKPG) is exposed as an elliptical body within the arcuate metamorphic belt sandwiched between the Singhbhum Granite in the south and the Chotonagpur Granite—Gneiss to the north. It consists of an older bimodal suite of grey gneiss and amphibolites, intruded by a younger unit of pegmatitic granite. The bimodal suite represents the basement to the enveloping metasediments.The average major-element chemistry of the grey gneiss conforms to the definition of trondhjemite and includes both low-Al₂O₃ and high-Al₂O₃ types. The amphibolites can be grouped into a low-MgO and a high-MgO type. Rocks of the younger unit range in composition from granodiorite to quartz monzonite. The two granitic units also differ significantly in their Rb, Sr and Ba contents, and in the REE distribution pattern. The grey gneiss shows a highly fractionated REE pattern and a distinct positive Eu anomaly, with Eu/Eu^* values increasing with increase in SiO₂ %. In samples of the younger granite, the REE pattern is less fractionated, with higher HREE abundance relative to the grey gneiss and usually shows a negative Eu anomaly. The two types of REE patterns in amphibolites are interpreted to represent the two broad groups identified on the basis of major element chemistry.On the basis of chemical data, a two-stage partial melting model for the genesis of grey gneiss is suggested, involving separation of hornblende and varying amounts of plagioclase in the residual phase. Varying amounts of plagioclase in the residuum result in the wide range of Al₂O₃ content of the partial melt from which the trondhjemites crystallised. Residual hornblende produces the highly fractionated REE pattern, but a relatively higher HREE content of the trondhjemites compared to those produced by separation of garnet in the residual phase. The high level of Ba together with moderate levels of Sr in the trondhjemites can also be explained by plagioclase in the residue, whose effectiveness in partitioning Ba compared to Sr is lower. Of the two groups of amphibolites, the low-MgO type shows relative depletion of LREE compared to the high-MgO type. It contains varying amounts of plagioclase and is tentatively suggested to represent the residue. The other group, with a slightly fractionated REE pattern (Ce_N/ Yb_N = 2.01), is generally considered to represent the source material for the trondhjemites. This may have been generated by 5–15% partial melting of mantle peridotites, containing higher concentrations of LIL elements than those which produced average Precambrian tholeiites. This first phase of partial melting resulted in the slightly fractionated REE pattern of these amphibolites. Derivation of the younger granitic unit from the trondhjemites can be ruled out on the basis of REE data alone. REE data suggest partial melting of metasediments to be the origin of these rocks. It is also possible that deeply buried volcanic rocks, similar to calc-alkaline components of greenstone belts, are the parent for this component.