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1.
E. Hegner  M. Klbl-Ebert  J. Loeschke 《Lithos》1998,45(1-4):395-411
Subsequent to high-pressure and temperature metamorphism of the axial zone of the Variscan foldbelt in central Europe at ca. 340 to 330 Ma, formation of lamprophyre dikes during transtensional tectonics may be viewed as the beginning of the post-collisional stage of the orogeny. We report the results of 40Ar/39Ar mica dating, major and trace element data, and isotope compositions for lamprophyre and rhyodacite samples from the southern Black Forest. The chemical compositions of these rocks shed light on the upper mantle and crust at the end of the Variscan orogeny. 40Ar/39Ar plateau ages for four phlogopite–biotite separates from lamprophyres indicate emplacement at 332 to 314 Ma. This event coincides with melting of the crust as indicated by 40Ar/39Ar biotite plateau ages of ca. 332 Ma for rhyodacite dikes which are probably related to coeval undeformed granites. Incompatible trace element patterns of the lamprophyre samples reveal the characteristics of evolved continental crust and are interpreted as evidence for melting of sediment in a subduction-modified mantle. Nd, Sr, and Pb isotope compositions indicate an enriched mantle source with Nd-values of −1.5 to −6.8 which is similar to Variscan crust. Significant contamination of the lamprophyric melts by Variscan crust can be ruled out as mantle-derived phlogopite phenocrysts have similar Nd-values as in the whole-rock samples. We propose that the isotope compositions and incompatible trace element characteristics of the lamprophyres were predominantly inherited from melted sediment. The isotope compositions of Variscan lamprophyres from western Europe suggest that enriched upper mantle was only partly delaminated when ascending hot mantle triggered melting of the lower crust, as has been invoked for the origin of post-collisional granites. The isotope compositions of Tertiary basalts and mantle xenoliths indicate a depleted upper mantle under western Europe, implying that the enriched Variscan material was efficiently removed and mixed into the convecting mantle.  相似文献   

2.
Analytical data on major elements and 31 trace elements in olivine nephelinites, nepheline basanites, basanitic alkali olivine basalts and their differentiates (tephrites, hawaiites, mugearites, benmoreites, latites, phonolites and trachytes) from Hegau, Kaiserstuhl, Rhön, Hessian Depression, Vogelsberg, Westerwald, Siebengebirge, E Eifel and Hocheifel are evaluated. They were based on 400 samples with new or unpublished data on about one third of the rocks. The Sr–Nd isotopic compositions for 78 rocks are included. The alkali basaltic volcanism is caused by adiabatic decompression of asthenospheric mantle updomed to a minimum depth of 50 km in connection with the Alpine continent collision. The chemical compositions of the primary basaltic melts from the different areas are similar containing about one hundred-fold enrichment of highly incompatible elements relative to the primitive mantle from partial melting of depleted and secondarily enriched peridotite. The elements Cs, K, Pb and Ti are specifically depleted in the basalts partly because of phlogopite being residual at partial melting. The Tertiary alkali basalts range in Nd-isotopic composition from 0.51288 to 0.51273 and in Sr-isotopic ratios from 0.7032 to 0.7042. These ranges indicate mixtures of HIMU, depleted and enriched mantle components in the metasomatically altered peridotite source which resembles that of certain ocean islands. The Nd-Sr-isotopic compositions of the Quaternary E Eifel are close to bulk Earth ratios. East and W Eifel plots differ distinctly from the Tertiary Hocheifel which is geographically intermediate. This isotopic difference, beside specific K/Na ratios, is probably caused by separate metasomatic pulses that immediately preceded the respective periods of volcanism. The metasomatically altered mantle had partly primitive mantle signatures (Nb/Ta, Zr/Sm and Th/U ratios) and partly ocean island (or MORB) source properties (Rb/Cs). A MORB source can be excluded because of the low K/Rb and high Th/U ratios. A correlation of D with 87Sr/86Sr in amphibole and phlogopite and a slightly larger 18O than in MORB is conformable with a seawater and crustal impact on the source of alkali basalts. Slightly higher than average water concentrations in the source of certain primary basaltic melts (indicated by amphibole phenocrysts in their basalts) are required for differentiation of these basalts in magma chambers of the upper crust. Model calculations are presented to explain compositions of differentiates which range from about 60% to about 20% residual melt. The latter are represented by phonolites and trachytes. The Nd- and Sr-isotopic signatures of the majority of differentiates indicate contamination by a granitic partial melt from the wall rocks of magma chambers. Olivine nephelinite magma was the common source of contaminated differentiates.  相似文献   

3.
本文报道了六合-仪征第三纪大陆碱性玄武岩十八个样品的REE、Rb、Ba、Sr、Nb、Zr、Ni、Cr、V、Sc、Y、Ga、Zn、Cu等痕量元素含量,讨论了该岩套的成因及其地幔源区的特征。石榴石橄榄岩型地幔源区经较小程度部分熔融形成了基性原始岩浆;其后经过橄榄石和单斜辉石为主的结晶分异作用,演化后的岩浆喷出地表形成玄武岩套。本区碱性玄武岩的地幔源区曾受近期富集作用影响,具有富集LREE等不相容元素的特征。  相似文献   

4.
New major and trace element data for the Permo–Triassic basalts from the West Siberian Basin (WSB) indicate that they are strikingly similar to the Nadezhdinsky suite of the Siberian Trap basalts. The WSB basalts exhibit low Ti/Zr (50) and low high-field-strength element abundances combined with other elemental characteristics (e.g., low Mg#, and negative Nb and Ti anomalies on mantle-normalised plots) typical of fractionated, crustally contaminated continental flood basalts (CFBs). The major and trace element data are consistent with a process of fractional crystallisation coupled with assimilation of incompatible-element-enriched lower crust. Relatively low rates of assimilation to fractional crystallisation (0.2) are required to generate the elemental distribution observed in the WSB basalts. The magmas parental to the basalts may have been derived from source regions similar to primitive mantle (OIB source) or to the Ontong Java Plateau source. Trace element modelling suggests that the majority of the analysed WSB basalts were derived by large degrees of partial melting at pressures less than 3 GPa, and therefore within the garnet-spinel transition zone or the spinel stability field.

It seems unlikely that large-scale melting in the WSB was induced through lithospheric extension alone, and additional heating, probably from a mantle plume, would have been required. We argue that the WSB basalts are chemically and therefore genetically related to the Siberian Traps basalts, especially the Nadezhdinsky suite found at Noril'sk. This suite immediately preceded the main pulse of volcanism that extruded lava over large areas of the Siberian Craton. Magma volume and timing constraints strongly suggest that a mantle plume was involved in the formation of the Earth's largest continental flood basalt province.  相似文献   


5.
Understanding the geochemical behavior of chalcophile elements in magmatic processes is hindered by the limited partition coefficients between sulfide phases and silicate melt, in particular at conditions relevant to partial melting of the hydrated, metasomatized upper mantle. In this study, the partitioning of elements Co, Ni, Cu, Zn, As, Mo, Ag, and Pb between sulfide liquid, monosulfide solid solution (MSS), and hydrous mantle melt has been investigated at 1200 °C/1.5 GPa and oxygen fugacity ranging from FMQ−2 to FMQ+1 in a piston-cylinder apparatus. The determined partition coefficients between sulfide liquid and hydrous mantle melt are: 750–1500 for Cu; 600–1200 for Ni; 35–42 for Co; 35–53 for Pb; and 1–2 for Zn, As, and Mo. The partition coefficients between MSS and hydrous mantle melt are: 380–500 for Cu; 520–750 for Ni; ∼50 for Co; <0.5 for Zn; 0.3–6 for Pb; 0.1–2 for As; 1–2 for Mo; and >34 for Ag. The variation of the data is primarily due to differences in oxygen fugacity. These partitioning data in conjunction with previous data are applied to partial melting of the upper mantle and the formation of magmatic-hydrothermal Cu–Au deposits and magmatic sulfide deposits.I show that the metasomatized arc mantle may no longer contain sulfide after >10–14% melt extraction but is still capable of producing the Cu concentrations in the primitive arc basalts, and that the comparable Cu concentrations in primitive arc basalts and in MORB do not necessarily imply similar oxidation states in their source regions.Previous models proposed for producing Cu- and/or Au-rich magmas have been reassessed, with the conclusions summarized as follows. (1) Partial melting of the oxidized (fO2 > FMQ), metasomatized arc mantle with sulfide exhaustion at degrees >10–14% may not generate Cu-rich, primitive arc basalts. (2) Partial melting of sulfide-bearing cumulates in the root of thickened lower continental crust or lithospheric mantle does not typically generate Cu- and/or Au-rich magmas, but they do have equivalent potential as normal arc magmas in forming magmatic-hydrothermal Cu–Au deposits in terms of their Cu–Au contents. (3) It is not clear whether partial melting of subducting metabasalts generates Cu-rich adakitic magmas, however adakitic magmas may extract Cu and Au via interaction with mantle peridotite. Furthermore, partial melting of sulfide-bearing cumulates in the deep oceanic crust may be able to generate Cu- and Au-rich magmas. (4) The stabilization of MSS during partial melting may explain the genetic link between Au-Cu mineralization and the metasomatized lithospheric mantle.The chalcophile element tonnage, ratio, and distribution in magmatic sulfide deposits depend on a series of factors. This study reveals that oxygen fugacity also plays an important role in controlling Cu and Ni tonnage and Cu/Ni ratio in magmatic sulfide deposits. Cobalt, Zn, As, Sn, Sb, Mo, Ag, Pb, and Bi concentrations and their ratios in sulfide, due to their different partitioning behavior between sulfide liquid and MSS, can be useful indices for the distribution of platinum-group elements and Au in magmatic sulfide deposits.  相似文献   

6.
The petrogenesis of the igneous complex in the Spanish Peaks region, Colorado, is reevaluated with Sr isotopic data (published and new) and new trace element data of REE and other transition metals. These data indicate that the diverse rock types ranging from ultrabasic lamprophyres to granitic porphyry of the igneous complex have independent origins.The lamprophyric magmas could be derived from the upper mantle by small degrees of partial melting of garnet peridotite source(s). Limited intra-type crystal fractionation is responsible for the small differences in REE and other elemental abundances. The intermediate syenodiorites were also derived by partial melting of some mantle sources with garnet as a residual phase. However, the major and trace element data suggest that the source for the syenodiorites is distinctly different from that of the lamprophyres. The narrow range of K/Rb ratios observed in minettes (449–464), camptonites (384–450) and syenodiorites (370–460) suggest that amphibole fractionation is not important in the generation of these intra- and intertype rocks.The granitic rocks were derived by melting of a lower crust whose composition varied from that of a granodioritic granulite to an amphibolite. It is suggested that the high alkali contents of the granitic porphyries are due to the introduction of alkalis into the source granulites shortly prior to the melting.  相似文献   

7.
The Ronda high temperature peridotite: Geochemistry and petrogenesis   总被引：2，自引：0，他引：2  
The Ronda peridotite in southern Spain is a large (~300 km2) exposure of upper mantle which provides direct information about mantle processes on a scale much larger than that provided by mantle xenoliths in basalt. Ronda peridotites range from harzburgite to lherzolite, and vary considerably in major element content, e.g., Al2O3 from 0.9 to 4.8%, and trace element abundances, e.g., Sr, Zr and La abundances vary by factors of 20 to 40. These compositional variations are systematic and correlate with (pyroxene + garnet)/olivine ratios and olivine compositions. The data are consistent with formation of residual peridotites by variable degrees of melting (~0 to 30%) of a compositionally homogeneous peridotite. None of the peridotites have geochemical characteristics of residues formed by extensive (?5%) fractional melting and the data can be explained by equilibrium (batch) melting, possibly with incomplete melt segregation in some samples. Based on compositional differences between Ronda peridotites, the segregated melts were picritic (12–22% MgO) with relative rare earth element abundances similar to mid-ocean ridge basalt (MORB). Prior to the melting event the Ronda peridotite body was a suitable source for MORB. The compositional characteristics of Ronda peridotites are consistent with diapiric rise of a fertile mantle peridotite with relatively small degrees of melting near the diapir-wall rock interface yielding residues of garnet iherzolite, and larger degrees of melting in the diapir interior yielding residues of garnet-free peridotite. Subsequently these residual rocks were recrystallized at sub-solidus conditions (Obata, 1980), and emplaced in the crust by thrusting (Lundeen, 1978).  相似文献   

8.
Mafic dike–granite associations are common in extensional tectonic settings and important and pivotal in reconstructing crust–mantle geodynamic processes. We report results of zircon U–Pb and hornblende 40Ar-39Ar ages and major-element and trace-element data for mafic dike–granite association from the northern West Junggar, in order to constrain their ages, petrogenesis, and geodynamic process. The mafic dike–granite association was emplaced in the early Devonian. The Xiemisitai monzogranites have high SiO2 contents and low MgO, Cr, and Ni concentrations, suggesting that they were mainly derived from crustal sources and were probably generated by partial melt of the juvenile mid-lower crust. The mafic dikes have low Mg# and Cr and Ni abundances, suggesting that they have experienced significant fractional crystallization. The Xiemisitai mafic dikes contain hornblende and biotite and display negative Nb–Ta–Ti anomalies, enrichment of LREEs and LILEs, and depletion of HREEs and HFSEs, consistent with an origin from a lithospheric mantle metasomatized by subducted slab-derived fluids. In addition, the Xiemisitai mafic dikes are plotted within melting trends with little to no garnet (Cpx: Grt = 6:1) in their source. The La/Yb versus Tb/Yb plot also indicates the presence of less than 1% residual garnet in the source region for the Xiemisitai mafic dikes. Therefore, it can be inferred that the Xiemisitai mafic dikes were generated at a correspondingly shallow depth, mostly within the spinel stability field. The Xiemisitai mafic dikes were most probably generated by the partial melting of the metasomatized lithospheric mantle at relatively shallow depths (<80 km). The Xiemisitai mafic dike–granite association could have been triggered by asthenospheric upwelling as a result of the rollback of the subducted Irtysh–Zaysan oceanic lithosphere.  相似文献   

9.
Mafic rocks from the Bamenda volcanic province along the Cameroon Volcanic Line have been dated from 17 to 0 Ma. Associated with some trachytes and rhyolites, this volcanism covers a period of more than 25 Ma. The studied rocks are basalts to mugearites. Most of them have been contaminated by continental crust during their transit to the surface. The oldest rocks are the most contaminated. One group of samples shows high Eu, Sr and Ba contents. This characteristic is not due to crustal contamination process, but has a mantle source origin. We argue that these characteristics have been acquired by mixing of melts formed by partial melting of mantle pyroxenites with melts formed in mantle peridotites. Such pyroxenites have been observed as mantle xenoliths in the Adamaoua province, and their chemical and isotopic compositions are consistent with such a model.  相似文献   

10.
The Cenozoic Mormon Mountain Volcanic Field (MMVF) of northern Arizona is situated in the transition zone between the Basin and Range and the Colorado Plateau. It is composed of alkalic to sub-alkalic basalts and calcalkalic andesites, dacites, and rhyodacites. Despite their spatial and temporal association, the basalts and the calcalkalic suite do not seem to be co-genetic. The petrogenesis of primitive MMVF basalts can be explained as the result of different degrees of partial melting of a relatively homogenous, incompatible element-enriched peridotitic source. The variety of evolved basalt types was the result of subsequent fractional crystallization of olivine, spinel, and clinopyroxene from the range of primitive basalts. Crustal contamination seems to have occurred, but affected only the highly incompatible element abundances. The formation of MMVF calcalkalic rocks is most readily explained by small to moderate amounts of partial melting of an amphibolitic lower crust. This source is LREE-enriched but depleted in Rb and relatively unradiogenic Sr (87Sr/86Sr 0.7040). Calcalkalic rhyodacites may also be derived from andesitic parents by fractional crystallization. The overall petrogenesis of the MMVF complex is the result of intra-plate volcanism where mantle-derived magmas intrude and pass through thick continental crust.  相似文献   

11.
K, Rb, Sr, Ba and rare earth elements of some Archean volcanic rocks from the Vermilion greenstone belt, northeast Minnesota, were determined by the isotopic dilution method. The characteristics of trace element abundances, supported by the field occurrences and major element chemistry, suggest that these volcanic rocks were formed in an ancient island arc system. A felsic rock is suggested to be derived by partial melting of a basaltic source, presumably in an ancient subduction zone.It is well known that the distribution coefficients (liquid/source) for the above trace elements are almost invariably greater than one. Continuous extraction of volcanic liquids from the upper mantle through geologic time would result in depletion of these elements in the upper mantle. However, all trace element abundances in many Archean volcanic rocks are almost identical to their modern equivalents. This gross constancy of trace element concentration in rocks of different geologic age raises some important questions as to the evolution of the upper mantle. It is proposed that the trace elements have been repeatedly and fully recycled in a restrictive and closed system of crust and upper mantle during the last three billion years (recycled mantle), or the trace elements have been replenished from the lower part of the mantle by some undefined process (replenished mantle). It is believed that interplay of both recycling and replenishment have been responsible for crust-mantle evolution in geological history.  相似文献   

12.
Archean metavolcanic rocks from three greenstone belts (Suomussalmi,Kuhmo and Tipasjärvi) of eastern Finland have been subjectto a detailed geochemical study which leads to a discussionof their petrogenesis and the problem of compositional heterogeneityin the Archean mantle. Lithostratigraphically, the greenstonebelts are roughly divided into a lower and an upper volcanicsequence. Rocks of komatiitic and tholeiitic compositions arerestricted to the lower sequence, while andesitic tuffs, dacite-rhyodacitelavas and minor basalts of alkaline affinity occur in the uppersequence. All rocks from the greenstone belts have been subjectto regional metamorphism of the upper greenschist facies tothe lower garnet amphibolite facies. Consequently, the geochemicaldistinction of original magma types and the discussion of petrogenesishave relied heavily on the abundances of less mobile elements,such as TiO2, rare earth elements (REE), and some transitionmetals (e.g. Ni and Cr). Using all the possible discriminants of major element compositions,we have concluded that two general magmatic series that existin the lower volcanic sequence might be distinguished by theparameter of TiO2 content: the komatiitic series is characterizedby having TiO2 1.0 per cent and the tholeiitic series by 1.0per cent. The general series do not imply that a cogenetic relationshiplinked only by fractional crystallization exists in each series. Several magmatic types could be distinguished by their characteristicREE distribution patterns. In general, the komatiitic rocksshow flat HREE (heavy REE) and flat or depleted LREE (lightREE) patterns; the tholeiitic rocks show fractionated patternswith some degree of LREE enrichment, whilst the acidic rocksdemonstrate highly fractionated patterns with significant HREEdepletion. Model calculations indicate that: (1) the komatiiticand the tholeiitic series have no clear genetic relationship;(2) some basaltic komatiites (MgO < 12 per cent) could havebeen derived by crystal fractionation from a melt of peridotitickomatiite composition (MgO 30 per cent), but others requirevarious degrees of partial melting from the same or differentsource regions to account for their trace element abundances;(3) both partial melting and fractional crystallization haveinterplayed for the production of various rocks within the tholeiiticseries; (4) three different types of source materials are proposedfor all magmas from the lower volcanic sequence. All three typeshave the same initial HREE (about 2x chondrites) but differentLREE (from very depleted to 2x, flat) abundances; (5) volcanicrocks of the upper volcanic sequence must have originated atgreat depths where garnet remains in the residue after partialmelting and melt segregation. The recognition of the strongly LREE-depleted mantle sources,deduced from the REE patterns of peridotitic komatiites fromFinland, Canada and Rhodesia, may suggest that this depletionis a worldwide phenomenon, and that the Archean upper mantleis as heterogeneous in composition as the modern upper mantle.The causal effect of the depletion might be related to the generationof some contemporaneous LREE-enriched tholeiitic rocks, or morelikely, to contemporaneous or previous continental crust formingevents.  相似文献   

13.
Garnet-facies continental mantle is poorly understood because the vast majority of mantle xenoliths in continental basalts are spinel peridotite. Peridotite xenoliths from Vitim (southern Siberia) and Mongolia provide some of the best samples of garnet and garnet-spinel facies off-craton lithospheric mantle. Garnets in those fertile to moderately depleted lherzolites show a surprisingly broad range of HREE abundances, which poorly correlate with modal and major oxide compositions. Some garnets are zoned and have Lu-rich cores. We argue that these features indicate HREE redistribution after the partial melting, possibly related to spinel-garnet phase transition on isobaric cooling. Most peridotites from Vitim have depleted to ultra-depleted Hf isotope compositions (calculated from mineral analyses: εHf(0) = +17 to +45). HREE-rich garnets have the most radiogenic εHf values and plot above the mantle Hf-Nd isotope array while xenoliths with normal HREE abundances usually fall within or near the depleted end of the MORB field. Model Hf isotope ages for the normal peridotites indicate an origin by ancient partial melt extraction from primitive mantle, most likely in the Proterozoic. By contrast, an HREE-rich peridotite yields a Phanerozoic model age, possibly reflecting overprinting of the ancient partial melting record with that related to a recent enrichment in Lu. Clinopyroxene-garnet Lu-Hf isochron ages (31-84 Ma) are higher than the likely eruption age of the host volcanic rocks (∼16 Ma). Garnet-controlled HREE migration during spinel-garnet and garnet-spinel phase transitions may be one explanation for extremely radiogenic 176Hf/177Hf reported for some mantle peridotites; it may also contribute to Hf isotope variations in sub-lithospheric source regions of mantle-derived magmas.  相似文献   

14.
The Mg numbers [100 Mg/(Mg+Fe) atomic ratios] of the Tertiary Monaro alkaline volcanics in southeastern Australia indicate that many of these alkali basalts, basanites and nephelinites have undergone only limited crystal fractionation, and that a few may represent unmodified, unfractionated primary magmas. Fractionation involves essentially olivine and clinopyroxene; fractionation trends are identified by plotting trace-element abundances against Mg number, and are then extrapolated linearly back into the primary magma field to yield estimates of the primary geochemistry of the three rock types.The nephelinites, basanites and alkali basalts are interpreted as a partial melting series derived from a peridotitic upper mantle. The estimated primary abundances of Pb,Th, Ga, V, Cr and Ni are essentially the same for the three rock types, but the estimated primary abundances of K2O, Rb, Sr, Ba, TiO2, Zr, Nb, P2O5, La Ce, Pr Nd, Y, Cu, and Zn-overlap considerably between the three rock types and the coherence of the incompatible elements as a group is not preserved in the overlaps. These patterns are best accounted for by postulating a patchy distribution of accessory phases such as amphibole, mica and apatite, in the source regions for the Monaro volcanics. Heterogeneities of this kind allow local variation in the volume of partial melt generated at the solidus, and offer a possible solution to magma segregation problems in the upper mantle.  相似文献   

15.
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16.
Volcanism along the northwest boundary of the Arabian Plate found in the Gaziantep Basin, southeast Turkey, is of Miocene age and is of alkaline and calc-alkaline basic composition. The rare earth element data for both compositional series indicates spinel–peridotite source areas. The rare earth and trace elements of the alkaline lavas originate from a highly primitive and slightly contaminated asthenospheric mantle; those of the calc-alkaline lavas originate from a highly heterogeneous, asthenospheric, and lithospheric mantle source. Partial melting and magmatic differentiation processes played a role in the formation of the petrological features of these volcanics. These rocks form two groups on the basis of their ~(87) Sr/~(86) Sr and ~(143) Nd/~(144) Nd isotopic compositions in addition to their classifications based on their chemical compositions(alkaline and calc-alkaline). These isotopic differences indicate a dissimilar parental magma. Therefore, high Nd isotope samples imply a previously formed and highly primitive mantle whereas low Nd isotope samples may indicate comparable partial melting of an enriched heterogeneous shallow mantle. Other isotopic changes that do not conform to the chemical features of these lavas are partly related to the various tectonic events of the region, such as the Dead Sea Fault System and the Bitlis Suture Zone.  相似文献   

17.
Seventeen basalts from Ocean Drilling Program (ODP) Leg 183 to the Kerguelen Plateau (KP) were analyzed for the platinum-group elements (PGEs: Ir, Ru, Rh, Pt, and Pd), and 15 were analyzed for trace elements. Relative concentrations of the PGEs ranged from ∼0.1 (Ir, Ru) to ∼5 (Pt) times primitive mantle. These relatively high PGE abundances and fractionated patterns are not accounted for by the presence of sulfide minerals; there are only trace sulfides present in thin-section. Sulfur saturation models applied to the KP basalts suggest that the parental magmas may have never reached sulfide saturation, despite large degrees of partial melting (∼30%) and fractional crystallization (∼45%).First order approximations of the fractionation required to produce the KP basalts from an ∼30% partial melt of a spinel peridotite were determined using the PELE program. The model was adapted to better fit the physical and chemical observations from the KP basalts, and requires an initial crystal fractionation stage of at least 30% olivine plus Cr-spinel (49:1), followed by magma replenishment and fractional crystallization (RFC) that included clinopyroxene, plagioclase, and titanomagnetite (15:9:1). The low Pd values ([Pd/Pt]pm < 1.7) for these samples are not predicted by currently available Kd values. These Pd values are lowest in samples with relatively higher degrees of alteration as indicated by petrographic observations. Positive anomalies are a function of the behavior of the PGEs; they can be reproduced by Cr-spinel, and titanomagnetite crystallization, followed by titanomagnetite resorption during the final stages of crystallization. Our modeling shows that it is difficult to reproduce the PGE abundances by either depleted upper or even primitive mantle sources. Crustal contamination, while indicated at certain sites by the isotopic compositions of the basalts, appears to have had a minimal affect on the PGEs. The PGE abundances measured in the Kerguelen Plateau basalts are best modeled by melting a primitive mantle source to which was added up to 1% of outer core material, followed by fractional crystallization of the melt produced. This reproduces both the abundances and patterns of the PGEs in the Kerguelen Plateau basalts. An alternative model for outer core PGE abundances requires only 0.3% of outer core material to be mixed into the primitive mantle source. While our results are clearly model dependent, they indicate that an outer core component may be present in the Kerguelen plume source.  相似文献   

18.
The mineralogy of Iherzolite inclusions in Victorian basanites indicates an upper mantle origin, but a range of temperatures from igneous to metamorphic (subsolidus) is indicated by the mineral compositions. Pyroxene textural features exhibit a slow cooling history consistent with isotopic evidence that these inclusions are accidental xenoliths. Clinopyroxene-rich inclusions (10–20 vol. % cpx) have higher abundances of Ca, Na, AI, Sc, V, Cr and heavy REE, lower Mg/Mg + Fe2+, lower Ni abundances, and more fayalitic olivines than clinopyroxene-poor inclusions (<5 vol. % cpx). A surprising result is that the refractory Mg-rich, clinopyroxenepoor inclusions contain the highest abundances of incompatible elements such as P, K, Ti, light REE, Th and U. We believe these inclusions are composed of two components (A and B). Component A determines the major element abundances and primary mineralogy of the inclusions. Based on Ni abundances component A is interpreted as a melting residue rather than a crystallization accumulate. Component B forms a small and varying portion of the inclusions, and it contributes P, K, Ti, light REE, Th and U. This component has the geochemical characteristics of a liquid formed in equilibrium with garnet.The following model is presented for the origin of Iherzolite inclusions. Residual Iherzolite (Component A) is left in the lithosphere after partial fusion, and it is later modified by a melt which has migrated to the top of the low velocity zone. Because this liquid (Component B) results from a small degree ( <6 per cent) of melting (probably limited by water abundance), and has equilibrated with garnet, it will be very enriched in P, K, Ti, light REE, Th and U. Subsequent cooling and recrystallization forms the present mineralogy. Finally, explosive volcanism, characteristic of silica-undersaturated magmas, incorporates mantle fragments (Iherzolite inclusions), and the increasing temperature and decreasing pressure during ascent causes incongruent melting of minor hydrous phases such as phlogopite and amphibole.  相似文献   

19.
Late Carboniferous (300–290 Ma) calc-alkaline basalts, andesites, and rhyolites typical of volcanic arc settings occur in the intermontane Saar-Nahe basin (SW Germany) within the Variscan orogenic belt. The volcanic rock suite was emplaced under a regime of tensional tectonics during orogenic collapse and its origin has been explained by melting of mantle and crust in the course of limited lithospheric rifting. We report major, trace and rare-earth-element data (REE), and Nd-Pb-Sr-O isotope ratios for a representative sample suite, which are fully consistent with an origin closely related to plate subduction. Major and trace element data define continuous melt differentiation trends from a precursor basaltic magma involving fractional crystallization of olivine, pyroxene, plagioclase, and magnetite typical of magma evolution in a volcanic arc. This finding precludes an origin of the andesitic compositions by mixing of mafic and felsic melts as can be expected in anorogenic settings. The mafic samples have high Mg numbers (Mg# = 65–73), and high Cr (up to 330 ppm) and Ni (up to 200 ppm) contents indicating derivation from a primitive parental melt that was formed in equilibrium with mantle peridotite. We interpret the geochemical characteristics of the near-primary basalts as reflecting their mantle source. The volcanic rocks are characterized by enrichment in the large ion lithophile elements (LILE), negative Nb and Ti, and positive Pb anomalies relative to the neighboring REE, suggesting melting of a subduction-modified mantle. Initial Nd values of −0.7 to −4.6, Pb, and 87Sr/86Sr(t) isotope ratios for mafic and felsic volcanics are similar and indicate partial melting of an isotopically heterogeneous and enriched mantle reservoir. The enrichment in incompatible trace elements and radiogenic isotopes of a precursor depleted mantle may be attributed to addition of an old sedimentary component. The geochemical characteristics of the Saar-Nahe volcanic rocks are distinct from typical post-collisional rock suites and they may be interpreted as geochemical evidence for ongoing plate subduction at the margin of the Variscan orogenic belt not obvious from the regional geologic context. Received: 3 August 1998 / Accepted: 2 January 1999  相似文献   

20.
Since Mesozoic time, Java and Bali have formed part of an evolving system of island arcs comprising the Sunda arc of Indonesia. The present tectonic setting is relatively simple with subduction occurring at the Java Trench to the south. A north-dipping Benioff seismic zone delineates an underthrust lithospheric slab to depths of approximately 600 km beneath the Java Sea. Quaternary lavas of the normal island arc association range from tholeiites to high-K calc-alkaline lavas over Benioff zone depths from 120–250 km, respectively. More abundant calc-alkaline lavas lie between these extremes. High-K alkaline lavas are found over Benioff zone depths in excess of 300 km.Both within and between these groups of rocks there are consistent spatial variations in the observed geochemistry. For approximately 200 rocks, incompatible elements such as K, Rb, Cs, Sr, Ba, light REE, U and Th show an increase in abundance of almost an order of magnitude with increasing depth to the seismic zone. Abundances of compatible elements show little consistent variation and trace elements such as Ni, Co, Cr, and Sc are characteristically depleted except in some of the alkaline lavas. Major element abundances in rocks of the normal island arc association show little variation, except for K and P, which both increase in abundance across the arc and Al, which shows a relative decrease.The major and trace element data are inconsistent with the derivation of the analyzed rocks by partial melting of the crustal component of the subducted lithosphere. On the other hand, low Ni abundances (20 ppm) in the basalts suggest that most of the lavas are fractionated and few if any represent primary mantle-derived melts. The spatial variations in the geochemistry of erupted lavas across Java and Bali are best explained by a combination of two processes: melting of a geochemically zoned mantle source and smaller degrees of partial melting of that material at progressively greater depths. Primary tholeiitic magmas could be formed by 20–25% melting at depths of 30–40 km, primary high-K calc-alkaline magmas by 5–15% melting at 40–60 km depth, and primary alkaline magmas by 5% melting at depths of 80–90 km. The geochemical zoning in the mantle, which is also manifested by increasing 87Sr/86Sr ratios in lavas across the arc, is interpreted to result from the addition of a small melt fraction derived from the crustal component of the subducted lithosphere.  相似文献   

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