The Arc Lavas of the Shirahama Group, Japan: Sr and Nd Isotopic Data Indicate Mantle-Derived Bimodal Magmatism

New Sr and Nd isotopic data are presented and integrated withprevious data for the Shirahama Group Mio-Pliocene medium-Kvolcanic are suite of south-central Honshu, Japan. Main resultsare: (1) The Shirahama lavas range in ⁸⁷Sr/⁸⁶Sr from 0.70315to 0.70337 and in ¹⁴³Nd/¹⁴⁴Nd from 0.51298 to 0.51306; the Srand Nd isotopic data cluster tightly within the mantle array,and all lie within an overlapping field of mid-ocean ridge basaltand ocean island basalt; (2) small differences exist among theShirahama tholeiitic series, calc-alkaline series and mixedlavas. The present isotopic data are consistent with a previouslypublished model, which proposes that chemical variations inmagmas of coexisting tholeiitic and calc-alkaline series areproduced through crystal fractionation from mantle-derived magmasof basalt and magnesian andesite, respectively. Moreover, thetholeiitic series and the calc-alkaline series are isotopicallyidentical. Thus, both magma series can be derived from a sourcemantle with the same isotopic composition, supporting the hypothesisof simultaneous generation of basalt and magnesian andesitemagmas from a single diapir rising through the mantle wedgeabove the subduction zone. The differences of water contentand temperature within the diapir are again thought to havebeen produced through dehydration and heating of an isotopicallyhomogeneous hydrous diapir. The isotopic data show that thehigh-SiO₂ lavas have the same isotopic compositions as moremafic lavas. These data and liquid lines of descent of the Shirahamamagmas suggest that even rhyolites can be produced by differentiationfrom mantle-derived magmas without crustal contamination. Analysesfrom 38 other arc volcanoes have been compiled to investigatethe intravolcano variability of ⁸⁷Sr/⁸⁶Sr. Twelve of these displayno intravolcano strontium isotopic variability, as is the casewith the Shirahama Group, but others show greater variationof ⁸⁷Sr/⁸⁶Sr from individual volcanic centers, presumably reflectingcrustal contamination. Most of the latter volcanoes are underlainby thick continental crust. It is noteworthy, however, thatthe greater variations of ⁸⁷Sr/⁸⁶Sr correlate with SiO₂ content;andesites or dacites, not basalts, from the same volcano havethe lowest ⁸⁷Sr/⁸⁶Sr, and these rocks are calc-alkaline in termsof FeO^*/MgO and SiO₂ Theoretically, assimilation of continentalcrust by the isotopically uniform Shirahama magmas could producethese relationships. Given that mantle-derived basalt and magnesianandesite both encounter continental crust on their ascent tothe surface, the hotter basalt magma would assimilate more crustalwallrocks than the cooler andesite, resulting in the basaltbeing more radiogenic. Fractional crystallization, magma mixing,and/or assimilation-fractional crystallization of these magmasin crustal magma chambers could produce large compositionalvariations, but the derivatives of the hotter basaltic magmas(tholeiitic series in the broad sense) would display greatercontamination than those derived from the cooler andesitic magmas(calc-alkaline series). ^*Telephone: 81-858-43-1215. Fax: 81-858-43-2184. e-mail: tamura{at}misasa.okayam-u.ac.jp     

海南岛新生代玄武质熔岩源区中再循环物质及其年龄的限定:来自Hf-Sr-Nd-Pb同位素的制约

再循环洋壳和沉积物在壳.幔循环过程中扮演着重要的角色。前人研究指出板片俯冲与海南地幔柱形成关系密切,然而地幔柱源区中是否存在再循环沉积物仍然不得而知。本文将首次报导海南岛新生代玄武质熔岩的Hf同位素,并将新的Sr-Nd-Pb同位素与前人数据相结合,限定再循环物质的组成及其年龄。与同位素地幔趋势相比,给定εNd时,海南岛玄武质熔岩的εHf值更低;而且Eu/Eu*>1、Sr/Sr*>1,与Al2O3、MgO都不存在相关性,说明Eu和Sr的正异常是继承了源区的特征,指示源区中存在再循环洋壳物质的参与。海南岛玄武质熔岩的Ce/Pb与εNd、εHf呈正相关关系,Nd/Pb与87Sr/86Sr呈负相关关系,它们都指向了沉积物端元。根据εHf-εNd模型和Pb同位素演化模型,推断源区中再循环洋壳和沉积物相对年轻,其年龄应小于1.0Ga。这些再循环洋壳和沉积物将进入深部地幔,并与地幔中的橄榄岩反应形成二阶段辉石岩,随着海南地幔柱不断上升而发生熔融,最终熔体喷发至地表形成海南岛玄武质熔岩。     

Isotopic and Geochemical Investigation of the Chilwa Island Carbonatite Complex, Malawi: Evidence for a Depleted Mantle Source Region, Liquid Immiscibility, and Open-System Behaviour

Initial Nd, Pb, and Sr isotopic data from carbonatites and associatedintrusive silica-undersaturated rocks from the early Jurassic,Chilwa Island complex, located in southern Malawi, central Africa,suggest melt derivation from a Rb/Sr- and Nd/Sm-depleted butTh/Pb- and U/Pb-enriched mantle source. Initial ¹⁴³Nd/¹⁴⁴Nd(0.51265–0.51270) isotope ratios from the Chilwa Islandcarbonatites are relatively constant, but their initial ⁸⁷Sr/⁸⁶Sr(0.70319–0.70361) ratios are variable. The ¹⁸O_smow (9.53–14.15%0)and ¹³C_PDB (–3.27 to –1.50%0) isotope ratios ofthe carbonates are enriched relative to the range of mantlevalues, and there is a negative correlation between ¹⁸O andSr isotope ratios. The variations in Sr, C, and O isotopic ratiosfrom the carbonatites suggest secondary processes, such as interactionwith meteoric groundwater during late-stage carbonatite activity.The initial ¹⁴³Nd/¹⁴⁴Nd (0.51246 0.51269) and initial ⁸⁷Sr/⁸⁶Sr(0.70344–0.70383) isotope ratios from the intrusive silicaterocks are more variable, and the Sr more radiogenic than thosefrom the carbonatites. Most of the Pb isotope data from Chilwa Island plot to the rightof the geochron and close to the oceanic regression line definedby MORBs and OIBs. Initial Pb isotopic ratios from both carbonatites(²⁰⁷Pb/²⁰⁴Pb 15.63–15.71; ²⁰⁶Pb/²⁰⁴Pb 19.13–19.78)and silicate rocks (²⁰⁷Pb/²⁰⁴Pb 15.61–15.72; ²⁰⁶Pb/²⁰⁴Pb18.18–20.12) show pronounced variations, and form twogroups in Pb-Pb plots. The isotopic variations shown by Nd, Pb, and Sr for the ChilwaIsland carbonatites and intrusive silicates suggest that thesemelts underwent different evolutionary histories. The chemicaldata, including isotopic ratios, from the carbonatites and olivinenephelinites are consistent with magmatic differentiation ofa carbonated-nephelinite magma. A model is proposed in whichdifferentiation of the carbonatite magma was accompanied byfenitization (metasomatic alteration) of the country rocks bycarbonatite-derived fluids, and subsequent alteration of thecarbonatite by hydrothermal activity. The chemical and isotopicdata from the non-nephelinitic intrusive silicate rocks reveala more complex evolutionary history, involving either selectivebinary mixing of lower-crustal granulites and a nephelinitemagma, or incremental batch melting of a depleted source andsubsequent crustal contamination.     

The Geochemistry of Lavas from the Gomores Archipelago, Western Indian Ocean: Petrogenesis and Mantle Source Region Characteristics

New mineral and bulk-rock analyses, as well as Nd, Sr and Pbisotope compositions are presented for lavas from Grande Comore,Moheli and Mayotte, thru of the four main islands of the ComoresArchipelago in the western Indian Ocean, and these data an usedto evaluate the petrogenesis, evolution and mantle source regioncharacteristics of Comorean lavas. The typically silica-undersaturated,alkaline lavas from all three islands can be grouped into twodistinct types: La Grille-type (LGT) lavas, which display strongrelative depletions in K, and Karthala-type (KT) lavas, whichdo not. With the exception of the lavas erupted by La Grillevolcano on Grande Comore, which exhibit the petrographic andgeochemical characteristics expected of primary mantle-derivedmagmas, all Comorean lavas analysed have experienced compositionalmodifications after they segregated from their source regions.Much of this variation can be explained quantitatively by fractionalcrystallization processes dominated by the fractionation ofolivineand clinopyroxene. Semi-quantitative modelling shows that theconsistent and fundamental difference in composition betweenK-depleted LGT lavas and normal KT lavas can be attributed topartial melting processes, provided amphibole is a residualmantle phase after extraction of LGT magmas at low degrees ofmelting. Low absolute abundances of the heavy rare earth elementsin LGT magmas are interpreted to reflect partial melting withinthe garnet stability field In contrast, KT magmas, which donot show relative K depletions, are considered to be the productsof somewhat larger degrees of partial melting of an amphibolefreesource at comparatively shallower depths. Whereas the Nd andSr isotopic compositions of Comorean lavas (which show a significantrange: ⁸⁷Sr/⁸⁶Sr = 0.70319–0.70393; ¹⁴³Nd/Nd = 0.51263–0.51288)bear evidence for a time-averaged depletion in incompatibleelements, the high incompatible element abundances of the lavasare interpreted to reflect the effects of a recent mantle enrichmentevent. At depths well within the garnet stability field thismantle enrichment is interpreted to have taken the form of modalmetasomatism with the introduction of amphibole (giving riseto the source of LGT magmas), whereas cryptic metasomatism tookplace at shallower levels (giving rise to the source of KT lavas).The Nd, Sr and Pb isotope signature of the majority of Comoreanlavas (both LGT and KT) is proposed to be the result of predominant4contributions from a somewhat heterogeneous source4 4 4 presentativeof the ambient sub-Comorean mantle, comprising a mixture betweena HIMU component and a component on the depleted portion ofthe mantle array (possibly the source of Indian Ocean MORB),with only limited contributions from an EM I plume component.The lavas erupted by Karthala volcano (the youngest Comoreanlavas), however, have significantly different isotopic compositionsfrom all other Comorean lavas (lower ¹⁴³Nd/¹⁴⁴Nd and higher⁸⁷Sr/⁸⁶Sr), suggesting increased contributions from the EM Icomponent. KEY WORDS: basalt petrogenesis; Comores; mantle geochemistry; ocean island basalts ^*Telephone: 27-21-6502921. Fax: 27-21-6503781 e-mail: alr{at}geology.uct.ac.za.     

The Role of Continental Crust and Lithospheric Mantle in the Genesis of Cameroon Volcanic Line Lavas: Constraints from Isotopic Variations in Lavas and Megacrysts from the Biu and Jos Plateaux

We present a combined Sr, Nd, Pb and Os isotope study of lavasand associated genetically related megacrysts from the Biu andJos Plateaux, northern Cameroon Volcanic Line (CVL). Comparisonof lavas and megacrysts allows us to distinguish between twocontamination paths of the primary magmas. The first is characterizedby both increasing ²⁰⁶Pb/²⁰⁴Pb (19·82–20·33)and ⁸⁷Sr/⁸⁶Sr (0·70290–0·70310), and decreasing_Nd (7·0–6·0), and involves addition of anenriched sub-continental lithospheric mantle-derived melt. Thesecond contamination path is characterized by decreasing ²⁰⁶Pb/²⁰⁴Pb(19·82–19·03), but also increasing ⁸⁷Sr/⁸⁶Sr(0·70290–0·70359), increasing ¹⁸⁷Os/¹⁸⁸Os(0·130–0·245) and decreasing _Nd (7·0–4·6),and involves addition of up to 8% bulk continental crust. Isotopicsystematics of some lavas from the oceanic sector of the CVLalso imply the involvement of a continental crustal component.Assuming that the line as a whole shares a common source, wepropose that the continental signature seen in the oceanic sectorof the CVL is caused by shallow contamination, either by continent-derivedsediments or by rafted crustal blocks that became trapped inthe oceanic lithosphere during continental breakup in the Mesozoic. KEY WORDS: crustal contamination; CVL; megacrysts; ocean floor; osmium isotopes     

滇西上地幔铅同位素演化模式及滇西富碱斑岩铅同位素组成的诠释

大量的Pb同位素数据资料表明,滇西上地幔铅具两阶段演化历史,但又不是很好地吻合Stacey-Kramers的两阶段模式.本文依据Stacey-Kramers建造两阶段模式的基本原理,结合滇西地区上地幔铅同位素组成资料,拟合出了能更好地反映滇西上地幔铅同位素演化历史的二阶段模式并应用此模式对滇西富碱斑岩及其相关岩石的铅同位素组成做出诠释.     

Contributions of Slab Fluid, Mantle Wedge and Crust to the Origin of Quaternary Lavas in the NE Japan Arc

Quaternary lavas from the NE Japan arc show geochemical evidenceof mixing between mantle-derived basalts and crustal melts atthe magmatic front, whereas significant crustal signals arenot detected in the rear-arc lavas. The along-arc chemical variationsin lavas from the magmatic front are attributable almost entirelyto geochemical variations in the crustal melts that were mixedwith a common mantle-derived basalt. The mantle-derived basaltshave slightly enriched Sr–Pb and depleted Nd isotopiccompositions relative to the rear-arc lavas, but the variationis less pronounced if crustal contributions are eliminated.Therefore, the source mantle compositions and slab-derived fluxesare relatively uniform, both across and along the arc. Despitethis, incompatible element concentrations are significantlyhigher in the rear-arc basalts. We examine an open-system, fluid-fluxedmelting model, assuming that depleted mid-ocean ridge basalt(MORB)-source mantle melted by the addition of fluids derivedfrom subducted oceanic crust (MORB) and sediment (SED) hybridsat mixing proportions of 7% and 3% SED in the frontal- and rear-arcsources, respectively. The results reproduce the chemical variationsfound across the NE Japan arc with the conditions: 0·2%fluid flux with degree of melting F = 3% at 2 GPa in the garnetperidotite field for the rear arc, and 0·7% fluid fluxwith F = 20% at 1 GPa in the spinel peridotite field beneaththe magmatic front. The chemical process operating in the mantlewedge requires: (1) various SED–MORB hybrid slab fluidsources; (2) variable amounts of fluid; (3) a common depletedmantle source; (4) different melting parameters to explain across-arcchemical variations. KEY WORDS: arc magma; crustal melt; depleted mantle; NE Japan; Quaternary; slab fluid     

Melt Enrichment of Shallow Depleted Mantle: a Detailed Petrological, Trace Element and Isotopic Study of Mantle-Derived Xenoliths and Megacrysts from the Cameroon Line

Major element, trace element and Sr–Nd–Pb isotopiccompositions of ultramafic xenoliths and megacrysts from thecontinental Cameroon line provide evidence for metasomatismof the upper most lithospheric mantle by enriched melts duringthe Mesozoic The megacrysts probably crystallized within thelower continental crust from melts similar to the host magmas.All the xenoliths originated as depleted residues after theextraction of basaltic melts, but some indicate evidence ofinteraction with enriched partial melts before entrainment.The U–Pb isotopic data on garnet are consistent with coolingthrough >900C at >300 Ma. The Sm–Nd isotope systematicsin constituent phases appear to have been in equilibrium ona xenolith scale at the time of entrainment, indicating derivationfrom mantle that remained at temperatures >600C until eruption.Spinel therzolies that show simple light rare earth element(LREE) depletions are characterized by isotopic compositionsthat are comparable with, but slightly more depleted than AtlanticN-MORB, suggesting that the unmetasomatized sub-continentallithosphere of the Cameroon line may be isotopically similarto that of sub-oceanic lithosphere. The Nd-depleted mantle modelages of these xenoliths are consistent with late Proterozoicdepletion, similar in age to much of the overlying continentalcrust. In contrast, samples that have LREE-enriched clinopyr-oxenes(La/Yb =4.7–9.4) contain trace amounts of amphibole, areenriched in U and have more radiogenic Pb and Sr. These xenolithsyield U–Pb and Sm–Nd model ages consistent withMesozoic enrichment, in agreement with the age of enrichmentof the source regions of the basalts, as deduced from Pb isotopiccompositions. Clinopyroxenes record three orders of magnitudeenrichment in U and LREE accompanied by progressive K depletionassociated with the growth of trace amphibole, with K/U ratiosthat range from 12000 to 1. The ratios of the trace elementsthought to have similar bulk D in mantle melting, Ce/Pb, Ba/Rband Nd/Sr ratios, display regional variations related to thetime integrated history of enrichments indicated by Nd isotopiccompositions. Mass balance calculations suggest that the meltsresponsible for the most recent enrichment of the lithospherehad higher La/Yb and U/Pb than Cameroon line host magmas, andwere probably the product of small degrees of partial meltingassociated with the earliest stages of the breakup of Pangea. KEY WORDS: Cameroon line; mantle xenoliths; megacrysts; REE; isotopic composition; trace element     

Trace Element and Isotopic Variations in Scottish and Irish Dinantian Volcanism: Evidence for an OIB-like Mantle Source

The Dinantian volcanic province of southern Scotland, northernEngland and parts of Ireland is represented by a large volumeof transitional to mildly alkaline rocks. Many (although notall) of its basic members display inter-regional variationsin incompatible element concentrations, particularly LREE, Zr,Nb, K, and Ba. Sr, Nd, and Pb isotopic data also show some minorinter-regional variations, although they are not as well-definedas those observed in the trace elements. Indeed, much of thevariation is intra-regional. Modelling of the basic rocks (4%MgO) using Ce/Y and Zr/Nb ratios reveals that fractional crystallizationand varying degrees of partial melting alone cannot explainthe compositional diversity. Models involving variable-depthmelting in the stability fields of both garnet and spinel, andgarnet exhaustion through progressive melting are equally untenable.The best model to fit the ratios is one involving variable-degreemelting superimposed on slight source region heterogeneity. Investigations of potential magma sources suggest that thisheterogeneity is not related to crustal contamination or toincorporation of relict slab material derived from a pre-existingsubduction zone (c. 50 Ma earlier) in the same region. Instead,the observed trace element and isotopic characteristics showmarked similarities to many modern ocean island basalts (OIB):a feature which suggests that the mantle source region was sub-lithospheric.It is suggested that the variations observed in basic Dinantianvolcanic rocks merely mirror on a local scale the variationsobserved in OIB globally, and that no other source is necessaryto explain the chemical diversity of Dinantian magmas. If thespeed of northward motion (15? of latitude between the LowerCarboniferous and Lower Permian) and the longevity of Dinantianvolcanism (c. 40 Ma) are taken into account, it is hardly surprisingthat such distinct chemical variations are observed: the magmasmay well have sampled an enormous volume of convecting sublithosphericmantle.     

Geochemistry of Lavas from Taal Volcano, Southwestern Luzon, Philippines: Evidence for Multiple Magma Supply Systems and Mantle Source Heterogeneity

Taal Volcano is a highly active center in the southwest Luzonvolcanic field. Recent eruptions are confined to Volcano Island,a plexus of cinder cones and tuff rings surrounding a centralcrater, occupying (and post-dating) a massive volcano-tectonicdepression resulting from multiple phases of collapse. Taallava series can be distinguished from each other by differencesin major and trace element trends and trace element ratios,indicating multiple magmatic systems associated with discretecenters in time and space. On Volcano Island, contemporaneous lava series range from typicallycalc-alkaline to iron-enriched. Major and trace element variationin these series can be modelled by fractionation of similarassemblages, with early fractionation of titano-magnetite inless iron-enriched series. However, phase compositional andpetrographic evidence of mineral-liquid disequilibrium suggeststhat magma mixing played an important role in the evolutionof these series. We interpret this to mean that mixing occurredalong a line of descent defined by fractional crystallization,with mixing occurring over larger compositional intervals inthe less iron-enriched series, consistent with numerical modelling. Between-series incompatible element ratio differences are notexplicable through differential partial melting of a homogeneoussource (also confirmed by variation in Pb isotopic ratios),suggesting a supply system from discrete melt zones in heterogeneousmantle.     

赣南中侏罗世玄武岩的Pb-Nd-Sr同位素地球化学研究：中生代地幔源区特征及构造意义

赣南龙南—寻邬地区余田群菖蒲组底部的玄武岩形成于中侏罗世(172．6～175．6Ma)，其Pb，Nd，Sr同位素组成的特征为：富放射性成因铅((^206Ph／^206Ph)i=17．872～18．653，(^207Pb／^204Pb)i=15．434～16．131，(^208pb／^204pb)i=37．837～39．194)，中等的εNd(t)(-0．4～+1．1，平均值为0．1)及较高的ISr(0．70835～0．71115)。玄武岩在Ph-Ph图解上均投影于NHRL上方，A7／4Pb值为0．19—61．7(平均值为22．1)，AS／4Pb值为59．2～101．5(平均值为71．03)，△Sr值为80．0～111．5(平均值为91．5)，表明存在典型的Dupal同位素异常。根据Sr-Nd，Sr-Ph，Nd-Pb和Pb-Pb相关特征，判明赣南玄武岩是由亏损地幔端元(DMM)和EMⅡ型富集地幔端元在源区混合形成的。按Sr-Nd双变量二元混合模型计算得出源区物质中亏损地幔端元和EMⅡ富集地幔端元所占份额分别为58％～64％和42％～36％。赣南地区呈东西向展布的中侏罗世双峰式火山岩带反映了华南板块内部在燕山早期发生的一起重要伸展构造事件。根据Ph-Nd-Sr同位素地球化学及构造特征，推测赣南中生代地幔源区中的EMⅡ富集地幔端元组分可能源自冈瓦纳古陆。     

The Depleted Mantle Component in Kerguelen Archipelago Basalts: Petrogenesis of Tholeiitic-Transitional Basalts From the Loranchet Peninsula

A geochemical study of 28 Ma tholeiitic to transitional basaltsfrom the Kerguelen Archipelago (Mont des Ruches and Mont Fontaine)indicates that three distinct magma types erupted within     

Isotopic Signatures of Neoproterozoic to Cambrian Ultrapotassic Syenitic Magmas,Northeastern Brazil: Evidence for an Enriched Mantle Source

Neoproterozoic to Cambrian ultrapotassic (K₂O up to 13 wt%) peralkalic alkali-feldspar-rich syenitic plutons were emplaced along the boundary between the Cachoeirinha-Salgueiro and Alto Pajeu tectonostratigraphic terranes of the Borborema structural province, northeastern Brazil. Syenite and alkalic pyroxenitic magmas coexisted in these plutons, which locally carry mica pyroxenite xenoliths. In the Triunfo batholith, the largest peralkalic pluton in the region, syenites and alkalic pyroxenites have high pyroxene-corrected δ¹⁸O values (+8.1 to + 8.5‰_SMOW in the syenite and +7.6 to + 7.7‰ in the alkalic pyroxenite), high δ³⁴S (+12.3‰_CDT in syenite and + 11.2‰_CDT in alkalic pyroxenite), high initial ⁸⁷Sr/⁸⁶Sr ratios (0.7098, syenite and alkalic pyroxenite data lying on the same Rb-Sr isochron), and low εNd (?15.3 to ?17.2 in syenite and ?16.1 in pyroxenite). Whole-rock δ¹⁸O_SMOW for mica pyroxenite xenoliths varies from +7.5 to +8.0‰_SMOW. Syenite, alkalic pyroxenite, and xenoliths all are enriched in large-ion lithophile elements (LILE). These geochemical and isotopic signatures suggest that the magmas were derived from an incompatible-element-enriched mantle source; this protolith probably resulted from hybridization by addition of crustal material via subduction at ～2.4 Ga, as estimated from Nd model ages. Partial melting of metasomatized material and magma emplacement at a late stage of the Brasiliano Orogeny (566 Ma) were controlled by mantle-deep shear zones during the amalgamation of the Cachoeirinha-Salgueiro and Alto Pajeu terranes.     

Similar V/Sc Systematics in MORB and Arc Basalts: Implications for the Oxygen Fugacities of their Mantle Source Regions

V/Sc systematics in peridotites, mid-ocean ridge basalts andarc basalts are investigated to constrain the variation of fO₂in the asthenospheric mantle. V/Sc ratios are used here to ‘seethrough’ those processes that can modify barometric fO₂determinations in mantle rocks and/or magmas: early fractionalcrystallization, degassing, crustal assimilation and mantlemetasomatism. Melting models are combined here with a literaturedatabase on peridotites, arc lavas and mid-ocean ridge basalts,along with new, more precise data on peridotites and selectedarc lavas. V/Sc ratios in primitive arc lavas from the Cascadesmagmatic arc are correlated with fluid-mobile elements (e.g.Ba and K), indicating that fluids may subtly influence fO₂ duringmelting. However, for the most part, the average V/Sc-inferredfO₂s of arc basalts, MORB and peridotites are remarkably similar(–1·25 to +0·5 log units from the FMQ buffer)and disagree with the observation that the barometric fO₂s ofarc lavas are several orders of magnitude higher. These observationssuggest that the upper part of the Earth's mantle may be stronglybuffered in terms of fO₂. The higher barometric fO₂s of arclavas and some arc-related xenoliths may be due respectivelyto magmatic differentiation processes and to exposure to large,time-integrated fluid fluxes incurred during the long-term stabilityof the lithospheric mantle. KEY WORDS: vanadium; scandium; oxygen fugacity; mantle; arcs     

基于PCA-SVM算法对稀土元素与稀土判别指标耦合数据集的铀矿床分类

不同类型铀矿床的沥青铀矿/晶质铀矿具有不同的稀土元素组成,其组成可作为判别铀矿床类型的重要指标。采用基于Python语言的主成分分析（principal component analysis,PCA）与支持向量机（support vector machines,SVM）结合的分类模型,对收集到的全球已知6种类型铀矿床的216组沥青铀矿/晶质铀矿稀土元素数据进行研究。以216组数据为训练集,通过数据清洗、特征缩放、PCA特征提取、网格搜索和交叉验证参数寻优构建SVM分类模型,对24组同变质型胡家峪晶质铀矿进行智能识别。研究结果显示：仅使用稀土元素的14维训练集最优模型判定胡家峪晶质铀矿类型的测试准确率为0.4%;由稀土元素、稀土总量、轻重稀土比、铕异常组成的17维训练集最优模型的测试准确率为75.0%,较14维训练集提高74.6%,模型泛化能力强;而通过传统稀土元素配分曲线、w（ΣREE）-（LREE/HREE）_N图解不能有效判定胡家峪晶质铀矿类型。本次研究表明,PCA-SVM算法对增有传统稀土判别指标数据集进行挖掘可有效厘定铀氧化物成因类型,效果明显优于单纯的稀土元素数据集以及传统的稀土配分曲线、w（ΣREE）-（LREE/HREE）_N图解。     

典型稀土矿区周边土壤中稀土元素含量及赋存形态研究

研究不同类型稀土矿区周边土壤中稀土元素(REE)的含量与形态特征,可为矿区周边污染环境治理提供理论支持与科学建议。本文采用欧盟BCR顺序提取法、电感耦合等离子体质谱测定的方法,对内蒙古白云鄂博稀土尾矿区和江西赣南稀土矿区周边6个土壤样品中15种稀土元素进行了含量及形态分析测定。结果表明:矿区周边土壤中稀土元素总量约为264～15955μg/g,明显高于全国土壤背景值(186μg/g),白云鄂博尾矿区周边土壤富集轻稀土元素,稀土元素主要以残渣态富集,占总含量的64.0%～89.4%,生物有效性较低,对环境影响较小;赣南矿区周边土壤富集重稀土元素,稀土元素的主要存在形式是弱酸提取态和可还原态,占总含量的70%以上,易发生迁移转化及对周边环境造成污染。土壤中稀土元素的形态分布与pH值有显著相关性,随着土壤pH值的降低,稀土元素的弱酸提取态含量不断升高,残渣态含量不断降低。     

济阳坳陷稀土元素特征及其在物源对比中的应用

物源是控制沉积物中REE组成最主要的因素，济阳坳陷区岩石稀土元素特征表明：①济阳坳陷古生界与华北地台其他地区同时代地层岩石的REE分布特征具有极大的相似性，这体现了晚古生代济阳坳陷区所处的整个华北地台区为一稳定的克拉通沉积盆地，地层横向分布稳定，具有一致的物源和构造背景；②济阳坳陷古生界为中生界的物源，反映了济阳坳陷区由古生代稳定地台型沉积到中生代山间盆地沉积的转变，中生代洼陷区的沉积主要来自对附近凸起区古生代地层的剥蚀；③新生界样品与中生界样品的REE分布模式具有很大的相似性，从一个侧面反映了济阳坳陷中生代与新生代的构造格局的转变，中生代接受沉积的部分洼陷区至古近纪成为供给物源的凸起区。     

Mafic Dyke Records of Paleoproterozoic Mantle Plume Activity in the Karelian Craton: U-Pb Baddeleyite/Zircon Geochronology and Sr-Nd Isotopic Data

正Mafic dykes preserved important information on mantle melting regimes in the early Earth history.Despite the fact that a large volume of geochronological data for mafic dykes was recently received,several important issues     

Source and Differentiation of Deccan Trap Lavas: Implications of Geochemical and Mineral Chemical Variations

The basalt stratigraphy of the Deccan Trap between MahabaleshwarGhat and Belgaum over-steps the basement from north to south.Sr-isotope and Zr/Nb ratios, and Sr, Rb, and Ba concentrationscorrelate portions of the post-Poladpur stratigraphy over 250km along the Western Ghats, thereby confirming a southerly componentof dip of 0?06?. At the southwestern margin, the stratigraphyextends upwards from the compositionally uniform Ambenali Formation(Cox & Hawkesworth, 1984) into a sequence of grossly heterogeneousflow units which have been allocated to the Mahabaleshwar andPanhala Formations (Lightfoot & Hawkesworth, 1988). TheMahabaleshwar Formation is represented only by a sequence ofhighly fractionated flows (termed the Kolhapur unit) with similar⁸⁷Sr/⁸⁶Sr₀ to the Mahabaleshwar (0?7045), but with Sr<240ppm and TiO₂>2?25%. Succeeding the Kolhapur unit are a seriesof flows with high ⁸⁷Sr/⁸⁶Sr₀ (0?7045-0?705), Zr/Nb > 13,and low Sr (< 200 ppm), which have been allocated to thePanhala Formation, and a group of flows with high ⁸⁷Sr/⁸⁶Sr₀(0?707–0?708) and Sr (>230), but trace element concentrationssimilar to the Mahabaleshwar Formation; these have been allocatedto the Desur unit of the Panhala. Geochemical variations in flows overlying the Ambenali definetwo distinct trends: one is attributed to gabbro fractionation,and the other to variations in the compositions of the parentalmagmas, and arguably their source regions. There is little evidencefor significant crustal contamination in these flows, and thedegree of fractionation and the composition of the phase extractare shown to vary along strike within the Mahabaleshwar Formation.The high TiO₂ content of Kolhapur unit flows is shown to bethe result of shallow-level gabbro fractionation, rather thanthe presence of a primitive high-Ti magma. Mahabaleshwar Formationbasalts exhibit a broad negative correlation between the degreeof fractionation and Sr-isotopic composition. The endmemberwith lower ⁸⁷Sr/⁸⁶Sr₀ has different Zr/Y from the Ambenali basalts,and would appear to have been generated by lower degrees ofmelting of a similar source. The other endmember has more radiogenicSr, lower Zr/Nb, similar Zr/Y, but higher mg-number. The simplestinterpretation is that these magmas were more primitive andhence hotter and more able to interact with the lithosphereen route to the surface, and that they then mixed to producethe Mahabaleshwar array. The Panhala Formation basalts ploton the Sr-Nd array defined by the Mahabaleshwar Formation, andthe Desur unit basalts plot on an extension of this array; thissuggests that the source characteristics are also lithospheric.The absolute elemental abundances may then be a function ofmelting and fractionation. We are impressed by the apparentswitch from crustal lithospheric contributions to mantle lithosphericcontributions through the stratigraphy, and suggest that this,together with the more protracted fractionation of the magma,reflects a change in the availability of the lithospheric componentsaccompanying the southerly migration of the volcanic edifice. ^* Present address: Geoscience Laboratories, Ontario Geological Survey, 11th Floor, 77, Grenville Street, Toronto, Ontario, M7A 1W4, Canada