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1.
Numerous isotope and trace element studies of mantle rocks and oceanic basalts show that the Earth’s mantle is heterogeneous. The isotopic variability in oceanic basalts indicates that most mantle sources consist of complex assemblages of two or more components with isolated long-term chemical evolution, on both global and local scales. The range in isotope and highly incompatible element ratios observed in oceanic basalts is commonly assumed to directly reflect that of their mantle sources. Accordingly, the end-points of isotope arrays are taken to represent the isotopic composition of the different components in the underlying mantle, which is then used to deduce the origin of mantle heterogeneity. Here, a melting model for heterogeneous mantle sources is presented that investigates how and to what extent isotope and trace element signatures are conveyed from source to melt. We model melting of a pyroxenite-bearing peridotite using recent experimental constrains for melting and partitioning of pyroxenite and peridotite. Identification of specific pyroxenite melting signatures allows finger-printing of pyroxenite melts and confirm the importance of lithological heterogeneity in the Earth’s mantle. The model results and the comparison of the calculated and observed trace element-isotope systematics in selected MORB and OIB suites (e.g. from the East Pacific Rise, Iceland, Tristan da Cunha, Gough and St.Helena) further show that factors such as the relative abundance of different source components, their difference in solidus temperature, and especially the extent, style and depth range of melt aggregation fundamentally influence the relationship between key trace element and isotope ratios (e.g. Ba/Th, La/Nb, Sr/Nd, La/Sm, Sm/Yb, 143Nd/144Nd). The reason for this is that any heterogeneity present in the mantle is averaged or, depending on the effectiveness of the melt mixing process, even homogenized during melting and melt extraction. Hence to what degree mantle heterogeneity is reflected in the erupted melts is not only a function of source and melting-induced variability. It also depends on the extent of mixing during melting and melt extraction and thus strongly on the relative incompatibility of the elements considered. The observed trace element variation in erupted melts can be greater or smaller than that of their mantle sources, depending on the incompatibility of the elements investigated. The isotopic variability in erupted melts, on the other hand, is generally smaller than that of their mantle source. Melt mixing during melt extraction consequently has an important influence on the relative extent of variation, and hence the degree of correlation between the isotope and trace element ratios. Overall fewer correlations between trace element and isotope ratios are expected whenever melts are extracted from a restricted depth range, as is the case for ocean island basalts, than for cases where melts are extracted over a larger depth interval (mid ocean ridges and especially ridge centered hotspots like Iceland). While the isotopic composition of the most enriched melts may correspond closely to those of the enriched source component, even the most depleted mid ocean ridge basalts are likely to underestimate the isotopic depletion of the depleted mantle component. These observations imply that using the chemical and isotopic range observed in oceanic basalts as directly representative of that in the corresponding mantle source can be misleading, since this assumption is strictly true only for homogeneous mantle sources. In addition to identifying source or partitioning-related differences in melts from different mantle sources, inferring the true composition, origin, and distribution of heterogeneous components in the Earth’s mantle therefore requires detailed knowledge about the mechanisms of melting and melt mixing during the melt extraction process. Only if these processes and their influence on the isotope-trace element relationship are understood, can the composition and origin of the different source components, and thus mantle heterogeneity, be accurately constrained. 相似文献
2.
R. Vollmer P. Ogden J. -G. Schilling R. H. Kingsley D. G. Waggoner 《Contributions to Mineralogy and Petrology》1984,87(4):359-368
Nd and Sr isotopic compositions and Rb, Sr, Sm and Nd concentrations are reported for madupites, wyomingites and orendites from the Pleistocene volcanic field of the Leucite Hills, Wyoming. All Leucite Hills rocks have negative εNd signatures, indicating derivation or contribution from an old light rare earth element (LREE) enriched source. In this respect they are similar to all occurrences of high potassium magmas so far investigated. But Sr isotopic variations are comparatively small and 87Sr/ 86Sr ratios are unusually low for high-K magmas (0.7053–0.7061, one sample excluded). These values suggest that the light REE enrichment of the source was not accompanied by a strong increase in Rb/Sr. Wyomingites and orendites are isotopically indistinguishable which is consistent with chemical and petrographic evidence for their derivation from a common magma series depending on emplacement conditions. Basic to ultrabasic madupites and more silicic wyomingites/orendites are distinct in their Nd isotopic variations (madupites: εNd= ?10.5 to ?12.3; wyomingites/orendites: εNd= ?13.7 to ?17.0) despite similar Sm/Nd ratios and complete overlap in 87Sr/86Sr. Selective or bulk assimilation of crustal material is unlikely to have significantly affected the Nd and Sr isotopic compositions of the magmas. The measured isotopic ratios are considered to reflect source values. The distinct isotopic characteristics of madupite and wyomingite/orendite magmas preclude their derivation by fractional crystallization, from a common primary magma, by liquid immiscibility or by partial melting of a homogeneous source. Two isotopically distinct, LREE enriched and slightly heterogeneous sources are required. Heterogeneities were most pronounced between magma sources from each volcanic centre (butte or mesa). The relationship between the madupite and wyomingite/orendite sources and their evolution is discussed on the basis of two simple alternative sets of models:
- a two-stage evolution model with an old enrichment event (a metasomatic event?) perhaps taking place during the stabilization of the Wyoming Craton 3.2 to 2.5 Gyr ago but not later than 1.2 Gyr ago or
- a mixing model involving mixing between one endmember with εNd near zero and another end-member with a strong negative εNd signature.
3.
The trace element compositions of S-type granites: evidence for disequilibrium melting and accessory phase entrainment in the source 总被引：4，自引：2，他引：2
Arnaud Villaros Gary Stevens Jean-François Moyen Ian S. Buick 《Contributions to Mineralogy and Petrology》2009,158(4):543-561
Within individual plutons, the trace element concentrations in S-type granites generally increase with maficity (total iron
and magnesium content and expressed as atomic Fe + Mg in this study); the degree of variability in trace element concentration
also expands markedly with the same parameter. The strongly peraluminous, high-level S-type granites of the Peninsular Pluton
(Cape Granite Suite, South Africa) are the product of biotite incongruent melting of a metasedimentary source near the base
of the crust. Leucogranites within the suite represent close to pure melts from the anatectic source and more mafic varieties
represent mixtures of melt and peritectic garnet and ilmenite. Trace elements such as Rb, Ba, Sr and Eu, that are concentrated
in reactant minerals in the melting process, show considerable scatter within the granites. This is interpreted to reflect
compositional variation in the source. In contrast, elements such as LREE, Zr and Hf, which are concentrated within refractory
accessory phases (zircon and monazite), show well-defined negative correlations with increasing SiO2 and increase linearly with increasing maficity. This is interpreted to reflect coupled co-entrainment of accessory minerals
and peritectic phases to the melt: leucocratic rocks cannot have evolved from the more mafic compositions in the suite by
a process of fractional crystallisation because in this case they would have inherited the zircon-saturated character of this
hypothetical earlier magma. Trace element behaviour of granites from the Peninsular Pluton has been modelled via both equilibrium
and disequilibrium trace element melting. In the disequilibrium case, melts are modelled as leaving the source with variable
proportions of entrained peritectic phases and accessory minerals, but before the melt has dissolved any accessory minerals.
Thus, the trace element signature of the melt is largely inherited from the reactants in the melting reaction, with no contribution
from zircon and monazite dissolution. In the equilibrium case, melt leaves the source with entrained crystals, after reaching
zircon and monazite saturation. A significant proportion of the rocks of the Peninsular Pluton have trace element concentrations
below those predicted by zircon and monazite saturation. In the case of the most leucocratic rocks all compositions are zircon
undersaturated; whilst the majority of the most mafic compositions are zircon oversaturated. However, in both cases, zircon
is commonly xenocrystic. Thus, the leucocratic rocks represent close to pure melts, which escaped their sources rapidly enough
that some very closely match the trace element disequilibrium melting model applied in this study. Zircon dissolution rates
allow the residency time for the melt in the source to be conservatively estimated at less than 500 years. 相似文献
4.
Bor-ming Jahn 《Contributions to Mineralogy and Petrology》1973,41(3):241-258
Twenty representative rocks ranging from lamprophyric to granitic composition, from the Spanish Peaks igneous Complex, south-central Colorado, were analyzed for Sr isotopic compositions and their concentrations of K, Rb, Sr and Ba. The various igneous rocks from this Cenozoic complex do not have a comagmatic relationship from the evidence of their Sr isotopic compositions. Due to the generally low Sr87/Sr86 isotopic ratios, the possibility of the highly radiogenic underlying Precambrian basement as the source of magma generation can be ruled out. The sources for the magmas of this igneous complex must be in the upper mantle or the lower crust. Model calculations using elemental distribution coefficients and assumed mantle materials suggest that the abundant lamprophyric magmas in this region could be derived from a phlogopite-bearing hornblende peridotite by a small degree of partial melting (<5%) at lower pressure environment (<50 km). Other possibilities for lamprophyric magma generation were also examined. The slightly higher Sr87/Sr86 ratios observed in the granitic rocks are interpreted as reflecting the nature of this source-the lower crust. Alternatively, they may suggest a limited contamination of the original liquid by upper crustal material. For the entire igneous complex, mixing of two independent magmas, lymprophyric and granitic, is suggested to be the mechanism responsible for the complicated and diverse chemical characteristics. 相似文献
5.
对华北克拉通南缘豫西燕山期具类似于板块俯冲带花岗岩成分变化规律（成分极性）的八宝山、柳关、后瑶峪花岗斑岩类的Pb、Sr、Nd同位素地球化学特征的研究,揭示了这些斑岩的主要物质来源是新太古代的太华群斜长角闪岩部分熔融产生的熔浆与地幔来源物质混合形成的产物。稀土元素含量非常低的八宝山花岗斑岩在岩石形成过程中有流体与其发生交代作用,由于交代及混合作用造成花岗斑岩类的Rb—Sr等时线多为假等时线;柳关花岗斑岩基本上完全由太华群的斜长角闪岩提供物质,豫西地区燕山期的花岗岩岩基其物质来源更为复杂,可能有宽坪群为其提供物质。 相似文献
6.
The Saldanha eruption centre, on the West Coast of South Africa, consists of 542 Ma, intracaldera, S-type, rhyolite ignimbrites divided into the basal Saldanha Ignimbrite and the partly overlying Jacob’s Bay Ignimbrite. Depleted-mantle Nd model ages suggest magma sources younger than the Early Mesoproterozoic, and located within the Neoproterozoic Malmesbury Group and Swartland complex metasedimentary and metavolcanic rocks that form the regional basement. The Sr isotope systematics suggest that the dominant source rocks were metavolcaniclastic rocks and metagreywackes, and that the magmas formed from separate batches extracted from the same heterogeneous source. No apparent magma mixing trends relate the Saldanha to the Jacob’s Bay Ignimbrites, or either of these to the magmas that formed the Plankiesbaai or Tsaarsbank Ignimbrites in the neighbouring Postberg eruption centre. The magmas were extracted from their source rocks carrying small but significant proportions of peritectic and restitic accessory minerals. Variations in the content of this entrained crystal cargo were responsible for most of the chemical variations in the magmas. Although we cannot construct a cogent crystal fractionation model to relate these groups of magmas, at least some crystal fractionation occurred, as an overlay on the primary signal due to peritectic assemblage entrainment (PAE). Thus, the causes of the cryptic chemical variation among the ignimbrite magmas of the Saldanha centre are variable, but dominated by the compositions of the parent melts and PAE. The preservation of clear, source-inherited chemical signatures, in individual samples, calls into question the common interpretation of silicic calderas as having been formed in large magma reservoirs, with magma compositions shaped by magma mingling, mixing, and fractional crystallization. The Saldanha rocks suggest a more intimate connection between source and erupted magma, and perhaps indicate that silicic magmas are too viscous to be significantly modified by magma-chamber processes. 相似文献
7.
G. Christofides D. Perugini A. Koroneos T. Soldatos G. Poli G. Eleftheriadis A. Del Moro A.M. Neiva 《Lithos》2007,95(3-4):243-266
Orogenic granitoids often display mineralogical and geochemical features suggesting that open-system magmatic processes played a key role in their evolution. This is testified by the presence of enclaves of more mafic magmas dispersed into the granitoid mass, the occurrence of strong disequilibrium textures in mineralogical phases, and/or extreme geochemical and isotopic variability.
In this contribution, intrusive rocks constituting the Sithonia Plutonic Complex (Northern Greece) are studied on the basis of mineral chemistry, whole-rock major, trace element geochemistry, and Sr and Nd isotopic composition. Sithonia rocks can be divided into a basic group bearing macroscopic (mafic enclaves), microscopic (disequilibrium textures), geochemical, and isotopic evidence of magma interaction, and an acid group in which most geochemical and isotopic features are consistent with a magma mixing process, but macroscopic and microscopic features are lacking.
A two-step Mixing plus Fractional Crystallization (MFC) process is considered responsible for the evolution of the basic group. The first step explains the chemical variation in the mafic enclave group: a basic magma, represented by the least evolved enclaves, interacted with an acid magma, represented by the most evolved granitoid rocks, to give the most evolved enclaves. The second step explains the geochemical variations of the remaining rocks of the basic group: most evolved enclaves interacted with the same acid magma to give the spectrum of rock compositions with intermediate geochemical signatures. A convection–diffusion process is envisaged to explain the geochemical and isotopic variability and the lack of macroscopic and petrographic evidence of magma interaction in the acid group.
The mafic magma is presumably the result of melting of a mantle, repeatedly metasomatized and enriched in LILE due to subduction events, whereas the acid magma is considered the product of partial melting of lower crustal rocks of intermediate to basaltic composition.
It is shown that Sithonia Plutonic Complex offers the opportunity to investigate in detail the complex interplay between geochemistry and magma dynamics during magma interaction processes between mantle and crustal derived magmas. 相似文献
8.
R. W. Carlson S. Esperança D. P. Svisero 《Contributions to Mineralogy and Petrology》1996,125(4):393-405
During the late Mesozoic, an unusually broad range of alkalic magma compositions was erupted along the southern border of the São Francisco craton of Brazil. This magmatic activity includes carbonatite, kimberlite, lamprophyre, lamproite, syenite and the largest known example of extrusive kamafugite, the Mata da Corda formation. To determine the nature of the sources of this magmatism, and their geochemical history, an Os isotope study along with major and trace element and Sr, Nd and Pb isotope analyses of kimberlitic, lamproitic and kamafugitic rocks from the Alto Paranaíba province of Brazil was undertaken. This complements recent geochemical and isotopic studies of these magmas. The Os isotope data for Alto Paranaíba samples point to a peridotitic lithospheric mantle source for the kimberlites and lamproites that was variably depleted in Re, presumably by melt removal at some time between the late Archean and mid-Proterozoic. These lithospheric peridotites experienced LIL-element enrichment by fluid/melt metasomatism at roughly 1 Ga, most likely during mobile belt formation along the western border of the São Francisco craton. Kamafugitic samples have very radiogenic Os, suggestive of mafic (e.g. pyroxenite, websterite, eclogite) source materials that again appear to have been stabilized in the lithospheric mantle of Brazil in the mid to late Proterozoic. The Os isotope evidence for lithospheric sources for the Alto Paranaíba activity, coupled with Sr, Nd and Pb isotopic characteristics that overlap those of the Walvis Ridge hot-spot trace indicate that the EM1 component in South Atlantic ocean island basalts most likely represents the influence of delaminated Brazilian lithospheric mantle mixed into mantle circulation beneath the South Atlantic and is not related to the plume(s) commonly associated with this ocean island magmatism. 相似文献
9.
双凤山基性侵入岩体位于松嫩-张广才岭地块南缘,其岩石组成主要为橄榄辉长岩.锆石LA-ICP-MS U-Pb定年显示该岩体形成于279±4 Ma.岩石矿物组成主要为橄榄石、单斜辉石、斜方辉石、高An值（80.1~87.9）斜长石以及以反应边形式存在的角闪石,矿物学特征指示其母岩浆为经历过充分流体交代的富水岩浆.全岩主微量元素组成揭示其源区物质组成为石榴子石二辉橄榄岩,部分熔融程度约20%,岩浆演化过程中经历了斜长石堆晶作用以及斜方辉石的结晶分异作用.全岩Sr-Nd同位素及锆石Hf同位素研究显示其（87Sr/86Sr）i=0.705 2~0.706 1,并具有正的εNd（t）值（0.9~1.3）和εHf（t）值（0~10.2）,表明其来源于亏损的地幔源区,并且岩浆上升过程中没有经历明显的地壳混染.微量元素和同位素特征综合反映岩浆源区经历了古亚洲洋俯冲沉积物熔体和流体交代作用的改造,但起主导作用的是流体.其地球化学特征总体显示MORB以及弧型玄武岩过渡的特征,暗示其形成于弧后伸展环境.研究区基性侵入岩地幔源区的不均一性主要受到古亚洲洋多期次俯冲作用析出熔/流体对上覆地幔楔不同程度的改造. 相似文献
10.
New Sr isotopic data on lavas and xenoliths from Somma-Vesuvius and other nearby volcanic areas (Phlegrean Fields and Ischia) are presented. Chemical and isotopic evidences show that not all the Phlegrean Fields rocks belong to the low K series, but some of them may be interpreted as low pressure differentiates of Somma magmas, i.e. as a part of the high K series. Two rock groups are defined in the Ischia low K series, which are well identified both in time and in chemical and isotopic features, and cannot be derived from the same magma source. The low K series in the studied area generally has lower Sr isotopic values than the high K series.Historical Vesuvian lavas show two distinct linear trends with negative slopes when87Sr/86Sr ratios are plotted against their ages of eruption. Such trends are interpreted to result from mixing of magmas in two separate reservoirs. Evidence from the Vesuvian ejecta shows that Somma-Vesuvius magmas underwent high or low pressure fractionation, in connection with different events of the Vesuvian activity. Distinct magma reservoirs developed episodically at different depths. Isotopic and geochemical evidences do not favour large scale assimilation of crustal materials by Somma-Vesuvius magmas, but instead appear to reflect mantle characteristics.A minimum of three different (inhomogeneous) source regions is necessary to account for the isotopic features of the studied rocks. 相似文献
11.
德兴斑岩铜矿成矿过程的氧、锶、钕同位素证据 总被引：10，自引：0，他引：10
为探讨德兴铜厂斑岩铜矿床成矿热液流体的来源、作用范围、时空演化及Cu在热液流体中的行为和迁移方向等重要问题，对采集于该矿床南部不同蚀变程度的岩石进行了氧、锶、钕同位素分析，结果表明，虽然与铜三斑岩铜矿成矿过程有关的热液流体至少有3种，包括高温岩浆流体、来自深部围岩的非岩浆流体和大气降水，但是起主导作用的是岩浆流体，钕、锶同位素在空间上的变化表明，在成矿流体形成及演化过程中，锶同位素值由斑岩体内部向围岩接触带有规律地升高（0.705→0.711），指示了矿床是因热液流体将成矿元素从岩体内部迁移到接触带附近富集而成的，它符合斑岩铜矿的正岩浆模式，而钕同位素则相对稳定，可作为蚀变侵入体岩浆起源的示踪剂。 相似文献
12.
We present a comprehensive geochemical data set for a suite of back-arc alkaline volcanic rocks from James Ross Island Volcanic Group (JRIVG), Antarctic Peninsula. The elemental and isotopic (Sr, Nd, Pb and Li) composition of these Cenozoic basalts emplaced east of the Antarctic Peninsula is different from the compositions of the fore-arc alkaline volcanic rocks in Southern Shetlands and nearby Bransfield Strait. The variability in elemental and isotopic composition is not consistent with the JRIVG derivation from a single mantle source but rather it suggests that the magma was mainly derived from a depleted mantle with subordinate OIB-like enriched mantle component (EM II). The isotopic data are consistent with mantle melting during extension and possible roll-back of the subducted lithosphere of the Antarctic plate. Magma contamination by Triassic–Early Tertiary clastic sediments deposited in the back-arc basin was only localized and affected Li isotopic composition in two of the samples, while most of the basalts show very little variation in δ7Li values, as anticipated for “mantle-driven” Li isotopic composition. These variations are difficult to resolve with radiogenic isotope systematics but Li isotopes may prove sensitive in tracking complex geochemical processes acting through the oceanic crust pile, including hydrothermal leaching and seawater equilibration. 相似文献
13.
Models of continental crustal magmagenesis commonly invoke theinteraction of mafic mantle-derived magma and continental crustto explain geochemical and petrologic characteristics of crustalvolcanic and plutonic rocks. This interaction and the specificmechanisms of crustal contamination associated with it are poorlyunderstood. An excellent opportunity to study the progressiveeffects of crustal contamination is offered by the compositeplutons of the Alaska Range, a series of nine early Tertiary,multiply intruded, compositionally zoned (Peridotite to granite)plutons. Large initial Sr and Nd isotopic contrasts betweenthe crustal country rock and likely parental magmas allow evaluationof the mechanisms and extents of crustal contamination thataccompanied the crystallization of these ultra-mafic throughgranitic rocks. Three contamination processes are distinguishedin these plutons. The most obvious of these is assimilationof crustal country rock concurrent with magmatic fractionalcrystallization (AFC), as indicated by a general trend towardcrustal-like isotopic signatures with increasing differentiation.Second, many ultramafic and mafic rocks have late-stage phenocrystreaction and orthocumulate textures that suggest interactionwith felsic melt. These rocks also have variable and enrichedisotopic compositions that suggest that this felsic melt wasisotopically enriched and probably derived from crustal countryrock. Partial melt from the flysch country rock may have reactedwith and contaminated these partly crystalline magmas followingthe precipitation and accumulation of the cumulus phenocrystsbut before complete solidification of the magma. This suggeststhat in magmatic mush (especially of ultramafic composition)crystallizing in continental crust, a second distinct processof crustal contamination may be super imposed on AFC or magmamixing involving the main magma body. Finally, nearly all rocks,including mafic and ultramafic rocks, have (87Sr/86Sr)i thatare too high, and (T) Nd that are too low, to represent theexpected isotopic composition of typical depleted mantle. However,gabbro xenoliths with typical depicted-mantle isotopic compositionsare found in the plutons. This situation requires either anadditional enriched mantle component to provide the parentalmagma for these plutons, or some mechanism of crustal contaminationof the parent magma that did not cause significant crystallizationand differentiation of the magma to more felsic compositions.Thermodynamic modeling indicates that assimilation of alkali-andwater-rich partial melt of the metapelite country rock by fractionating,near-liquidus basaltic magma could cause significant contaminationwhile suppressing significant crystallization and differentiation. KEY WORDS: crustal contamination; Alaska Range; isotope geochemistry; zoned plutons; assimilation
*Corresponding author. e-mail: preiners{at}u.washington.edu; fax: (206) 543-3836. 相似文献
14.
Subduction-related Quaternary volcanic rocks from Solander and Little Solander Islands, south of mainland New Zealand, are porphyritic trachyandesites and andesites (58.20–62.19 wt% SiO2) with phenocrysts of amphibole, plagioclase and biotite. The Solander and Little Solander rocks are incompatible element enriched (e.g. Sr ~931–2,270 ppm, Ba ~619–798 ppm, Th ~8.7–21.4 ppm and La ~24.3–97.2 ppm) with MORB-like Sr and Nd isotopic signatures. Isotopically similar quench-textured enclaves reflect mixing with intermediate (basaltic-andesite) magmas. The Solander rocks have geochemical affinities with adakites (e.g. high Sr/Y and low Y), whose origin is often attributed to partial melting of subducted oceanic crust. Solander sits on isotopically distinct continental crust, thus excluding partial melting of the lower crust in the genesis of the magmas. Furthermore, the incompatible element enrichments of the Solander rocks are inconsistent with partial melting of newly underplated mafic lower crust; reproduction of their major element compositions would require unrealistically high degrees of partial melting. A similar argument precludes partial melting of the subducting oceanic crust and the inability to match the observed trace element patterns in the presence of residual garnet or plagioclase. Alternatively, an enriched end member of depleted MORB mantle source is inferred from Sr, Nd and Pb isotopic compositions, trace element enrichments and εHf ? 0 CHUR in detrital zircons, sourced from the volcanics. 10Be and Sr, Nd and Pb isotopic systematics are inconsistent with significant sediment involvement in the source region. The trace element enrichments and MORB-like Sr and Nd isotopic characteristics of the Solander rocks require a strong fractionation mechanism to impart the high incompatible element concentrations and subduction-related (e.g. high LILE/HFSE) geochemical signatures of the Solander magmas. Trace element modelling shows that this can be achieved by very low degrees of melting of a peridotitic source enriched by the addition of a slab-derived melt. Subsequent open-system fractionation, involving a key role for mafic magma recharge, resulted in the evolved andesitic adakites. 相似文献
15.
江西会昌盆地晚白垩世站塘高钠埃达克质岩石的地球化学特征及岩石成因 总被引：5，自引：3，他引：2
江西会昌盆地晚白垩世喷发的站塘安山岩,其形成与晚中生代岩石圈伸展和玄武质岩浆的底侵作用有关。这些岩石是高Na(6.59%～8.46%Na2O)、高Al的奥长花岗质岩石,具有与埃达克岩相似的高Sr和Ba、低Y和HREE、高Sr/Y和La/Yb比等特点。与埃达克岩相比,它们的Na2O较高而CaO较低,其εNd(t)值-2.3～-3.8和87Sr/86Sr初始比值0.707～0.708也与具大洋同位素组成特征的埃达克岩有明显区别。这些化学的和同位素特征,表明它们并非消减板片部分熔融的产物。站塘埃达克质岩浆可能源自底侵玄武质下地壳,其异常的高Na和低Ca特点反映其源岩成分的特殊性。因其成分与由实验产生的富碱玄武岩部分熔融体组成相当,因此,我们认为站塘高钠安山质岩浆可能是富碱玄武质岩石部分熔融的产物。 相似文献
16.
The Rhön area as part of the Central European Volcanic Province (CEVP) hosts an unusual suite of Tertiary 24-Ma old hornblende-bearing alkaline basalts that provide insights into melting and fractionation processes within the lithospheric mantle. These chemically primitive to slightly evolved and isotopically (Sr, Nd, Pb) depleted basalts have slightly lower Hf isotopic compositions than respective other CEVP basalts and Os isotope compositions more radiogenic than commonly observed for continental intraplate alkaline basalts. These highly radiogenic initial 187Os/188Os ratios (0.268–0.892) together with their respective Sr–Nd–Pb isotopic compositions are unlikely to result from crustal contamination alone, although a lack of Os data for lower crustal rocks from the area and limited data for CEVP basalts or mantle xenoliths preclude a detailed evaluation. Similarly, melting of the same metasomatized subcontinental lithospheric mantle as inferred for other CEVP basalts alone is also unlikely, based on only moderately radiogenic Os isotope compositions obtained for upper mantle xenoliths from elsewhere in the province. Another explanation for the combined Nd, Sr and Os isotope data is that the lavas gained their highly radiogenic Os isotope composition through a mantle “hybridization”, metasomatism process. This model involves a mafic lithospheric component, such as an intrusion of a sublithospheric primary alkaline melt or a melt derived from subducted oceanic material, sometime in the past into the lithospheric mantle where it metasomatized the ambient mantle. Later at 24 Ma, thermal perturbations during rifting forced the isotopically evolved parts of the mantle together with the peridotitic ambient mantle to melt. This yielded a package of melts with highly correlated Re/Os ratios and radiogenic Os isotope compositions. Subsequent movement through the crust may have further altered the Os isotope composition although this effect is probably minor for the majority of the samples based on radiogenic Nd and unradiogenic Sr isotope composition of the lavas. If the radiogenic Os isotope composition can be explained by a mantle-hybridization and metasomatism model, the isotopic compositions of the hornblende basalts can be satisfied by ca. 5–25% addition of the mafic lithospheric component to an asthenospheric alkaline magma. Although a lack of isotope data for all required endmembers make this model somewhat speculative, the results show that the Re–Os isotope system in continental basalts is able to distinguish between crustal contamination and derivation of continental alkaline lavas from isotopically evolved peridotitic lithosphere that was contaminated by mafic material in the past and later remelted during rifting. The Hf isotopic compositions are slightly less radiogenic than in other alkaline basalts from the province and indicate the derivation of the lavas from low Lu–Hf parts of the lithospheric mantle. The new Os and Hf isotope data constrain a new light of the nature of such metasomatizing agents, at least for these particular rocks, which represent within the particular volcanic complex the first product of the volcanism. 相似文献
17.
本文报道了浙江省21个中生代火成岩的Nd-Sr同位素组成,其中火山岩的εNd值为-12.6——4.9,ISr值为0.70613-0.71079,tDM年龄为1945-1296Ma;花岗岩类的εNd值为-12.9——5.8,ISr值为0.70533-0.71208,tDM年龄为1900-1230Ma,表明两者具有相似的同位素组成。这种相似性在同一火山-侵入杂岩体中表现更为明显,意味着两者在时、空、源方面具有同一性。与扬子地块的相比,华夏地块的中生代火成岩具有较低的εNd值,较高的ISr值和较古老的Nd模式年龄,这种差异可能主要同这两个区域内基底变质岩在形成时代和成分上的差异有关。通过Sm-Nd同位素组成的对比研究,笔者认为,浙江境内的中生代火成岩可能主要是由基底变质沉积岩衍生的。原始岩浆的形成可能同中、下地壳岩石的熔融有关。 相似文献
18.
Sandro Conticelli Riccardo Avanzinelli Sara Marchionni Simone Tommasini Leone Melluso 《Mineralogy and Petrology》2011,103(1-4):123-148
The Radicofani Volcano is characterised by few lava flows, a cinder cone and a denudated neck, and is part of the Tuscan Magmatic Province, the northernmost volcanic region of the Italian peninsula. In spite of the short time span of activity, a large time-dependant chemical and isotopic variability is observed. Most of the rocks of the Radicofani volcano are ultrapotassic shoshonites associated to younger basaltic andesites, found at the bottom of the neck. K2O contents are positively correlated with trace element and isotopic variations. Shoshonitic and high-K calc-alkaline rocks of the Radicofani volcano are significantly different from shoshonites occurring in association with leucite-bearing ultrapotassic rocks in the southernmost portion of the Roman Magmatic Province. The studied rocks are characterised by high, but variable, levels of incompatible trace elements with a subduction-related signature, with troughs at Ba, Ta, Nb, and Ti, and peaks at Cs, K, Th, U, and Pb. Initial values of 87Sr/86Sr range from 0.71333 to 0.71588, 143Nd/144Nd ranges from 0.512050 to 0.512183, while the lead isotope ratios vary between 18.672 and 18.716 for 206Pb/204Pb, 15.665 to 15.696 for 207Pb/204Pb, and 39.981 to 39.081 for 208Pb/204Pb. Ultrapotassic shoshonites show the highest incompatible trace element contents coupled with the highest 87Sr/86Sr and the lowest 143Nd/144Nd. On the basis of geochemical and isotopic signatures it is argued that magmas were generated in a modified lithospheric peridotitic source containing metasomatic veins generated by K-rich melts from recycled sediments within the mantle via subduction. A further metasomatic event generated by slab-derived fluids pervasively enriched the peridotitic source. Partial melting of the veins produced leucite-free ultrapotassic magmas (i.e. lamproite), and was triggered by rising of the isotherms after the orogenic front migrated eastward in the Italian Peninsula. Further rise of the isotherms induced larger degrees of partial melting inducing melting of the surrounding wall peridotite. The variation of the degree of partial melting of such a heterogeneous peridotitic source produced a wide spectrum of magma compositions, which mimic a mixing line between two components: ultrapotassic magma from partial melting of the metasomatic vein and a basaltic andesitic magma from partial melting of the surrounding peridotite. 相似文献
19.
汉诺坝玄武岩中地幔岩捕掳体REE和Sr,Nd同位素地球化学 总被引：20，自引：3，他引：20
本文报道汉诺坝玄武岩中地幔岩捕掳体的ＲＥＥ丰度和Ｓｒ、Ｎｄ同位素组成。不同岩石类型的ＲＥＥ配分模式和同位素组成反映地幔部分熔融程度和交代作用过程。二辉橄榄岩亏损轻稀土，是原始地幔经不同程度部分熔融的残留体。方辉橄榄岩具Ｕ型ＲＥＥ配分模式，是强烈亏损的地幔岩被熔体非化学平衡交代的结果。二辉岩脉状体富轻、中稀土，它同与脉状体接触的二辉橄榄岩可达化学平衡或近于化学平衡，而二辉岩脉状体的形成与玄武岩岩浆无成因关系。据对二辉岩脉状体和不含脉状体橄榄岩的Ｓｍ－Ｎｄ同位素定年，这种脉状体形成于３００Ｍａ左右。 相似文献
20.
John Maclennan 《Geochimica et cosmochimica acta》2008,72(16):4159-4176
The lead isotope and trace element compositions of a suite of olivine-hosted melt inclusions in primitive lava flows from the Reykjanes Peninsula in Iceland show extreme variability. Much of this variability is present in the composition of inclusions from one hand specimen of Háleyjabunga, a depleted picrite lava shield that erupted 13 ka. 208Pb/206Pb compositions in this sample span 50-90% of the total range found in Atlantic MORB, indicating that high-amplitude compositional heterogeneity is present in the mantle source of melts that aggregated to form a single eruption. The trace element and isotopic trends in the melt inclusions are coincident with those in whole rock samples from young lava flows of the Reykjanes Peninsula, and extend the total range of variation towards more depleted compositions. The incompatible trace element and lead isotope compositions of the inclusions are strongly coupled and lie close to binary mixing trends between the extreme melt inclusion compositions. These relationships indicate that the trace element variation in the melt inclusions reflects heterogeneity in the composition of the mantle source entering the melting region under the Reykjanes Peninsula. Large positive Sr concentration anomalies are present in three of the inclusions, but do not correlate with indicators of mantle melting or source variations and are likely to arise by reaction with plagioclase during crustal storage. Fractional melting of heterogeneous mantle is predicted to generate melts with a wide range of compositions, filling a large volume in trace element-isotope space. However, the compositional variations observed in the melt inclusions lie close to binary mixing curves. These observations may be accounted for by a two-stage model of melt mixing. The first stage occurs in porous channels that transport melt in the mantle and takes place before inclusion entrapment. This mixing stage generates a bimodal distribution of melt compositions that is supplied from the channels to sub-Moho and lower crustal magma lenses. The second stage of mixing occurs in these chambers, producing the binary mixing trends recorded in the inclusion compositions. The distribution of isotopic compositions observed in the melt inclusions and whole rock samples from the Reykjanes Peninsula is therefore controlled by melt mixing. These results have important implications for the interpretation of basalt composition in terms of distinct compositional entities within the upwelling solid mantle under mid-ocean ridges and ocean islands. 相似文献