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1.
Abstract Geochemical data on Baegryeong Island spinel peridotites found in Miocene alkali basalt provide the information for lithosphere composition, chemical processes, equilibrium pressure and temperature conditions. Spinel peridotite xenoliths, showing transitional textures between protogranular and porpyroclastic textures, were accidentally trapped by the ascending alkali basalt magma. The xenoliths originate at depths from 50 to 70 km with a temperature range from 800 to 1100°C. The variations of modal and mineral compositions of the spinel peridotite xenoliths indicate that the xenoliths have undergone 1–10% fractional melting. The spinel peridotites from Baegryeong Island have undergone cryptic mantle metasomatism subsequent to melt extraction. Metasomatic agent of enriched spinel peridotite xenoliths was carbonatite melt. 相似文献
2.
Csaba Szabó Károly Hidas Enik&#; Bali Zoltán Zajacz István Kovács Kyounghee Yang Tibor Guzmics Kálmán Török 《Island Arc》2009,18(2):375-400
In this paper we present a detailed textural and geochemical study of two equigranular textured amphibole-bearing spinel lherzolite xenoliths from Szigliget, Bakony–Balaton Highland Volcanic Field (BBHVF, western Hungary) containing abundant primary silicate melt inclusions (SMIs) in clinopyroxene rims and secondary SMIs in orthopyroxene (and rarely spinel) along healed fractures. The SMIs are dominantly composed of silicate glass and CO2 -rich bubbles. Clinopyroxene and orthopyroxene are zoned in both studied xenoliths, especially with respect to Fe, Mg, Na, and Al contents. Cores of clinopyroxenes in both xenoliths show trace element distribution close to primitive mantle. Rims of clinopyroxenes are enriched in Th, U, light rare earth elements (LREEs) and medium REEs (MREEs). Amphiboles in the Szg08 xenolith exhibit elevated Rb, Ba, Nb, Ta, LREE, and MREE contents. The composition of silicate glass in the SMIs covers a wide range from the basaltic trachyandesite and andesite to phonolitic compositions. The glasses are particularly rich in P2 O5 . Both primary and secondary SMIs are strongly enriched in incompatible trace elements (mostly U, Th, La, Zr) and display a slight negative Hf anomaly. The development of zoned pyroxenes, as well as the entrapment of primary SMIs in the clinopyroxene rims, happened after partial melting and subsequent crystallization of clinopyroxenes, most probably due to an interaction between hot volatile-bearing evolved melt and mantle wall-rocks. This silicate melt filled microfractures in orthopyroxenes (and rarely spinels) resulting in secondary SMIs. 相似文献
3.
A correlary of sea floor spreading is that the production rate of ocean ridge basalts exceeds that of all other volcanic rocks on the earth combined. Basalts of the ocean ridges bring with them a continuous record in space and time of the chemical characteristics of the underlying mantle. The chemical record is once removed, due to chemical fractionation during partial melting. Chemical fractionations can be evaluated by assuming that peridotite melting has proceeded to an olivine-orthopyroxene stage, in which case the ratios of a number of magmaphile elements in the extracted melt closely match the ratios in the mantle. Comparison of ocean ridge basalts and chondritic meteorites reveals systematic patterns of element fractionation, and what is probably a double depletion in some elements. The first depletion is in volatile elements and is due to high accretion temperatures of a large percentage of the earth from the solar nebula. The second depletion is in the largest, most highly charged lithophile elements (“incompatible elements”), probably because the mantle source of the basalts was melted previously, and the melt, enriched in these elements, was removed. Migration of melt relative to solid under ocean ridges and oceanic plates, element fractionation at subduction zones, and fractional melting of amphibolite in the Precambrian are possible mechanisms for depleting the mantle in incompatible elements. Ratios of transition metals in the mantle source of ocean ridge basalts are close to chondritic, and contrast to the extreme depletion of refractory siderophile elements, the reason for which remains uncertain. Variation of ocean ridge basalt chemistry along the length of the ridge has been correlated with ridge elevation. Thus chemically anomalous ridge segments up to 1000 km long appear to broadly coincide with regions of high magma production (plumes, hot spots). Basalt heterogeneity at a single location indicates mantle heterogeneity on a smaller scale. Variation of ocean ridge basalt chemistry with time has not been established, in fact, criteria for recognizing old oceanic crust in ophiolite terrains are currently under debate. The similarity of rare earth element patterns in basalt from ocean ridges, back-arc basins, some young island arcs, and some continental flood basalts illustrates the dangers of tectonic labeling by rare earth element pattern. 相似文献
4.
J. D. Blundy J. A. C. Robinson B. J. Wood 《Earth and Planetary Science Letters》1998,160(3-4):493-504
Trace element partitioning between clinopyroxene and melt was investigated experimentally under conditions appropriate to near-solidus melting of spinel lherzolite in the upper mantle. Starting material was a high-Na, Al basalt glass previously shown to be a very low degree (1%) partial melt of spinel lherzolite at 1.5 GPa, 1269°C [Robinson et al., Earth Planet. Sci. Lett., in press]. The experiment was run with a spinel seed under sub-liquidus conditions (1255°C) to ensure clinopyroxene crystallisation. The experimental clinopyroxene composition is consistent with equilibrium close to the solidus of fertile mantle lherzolite, most notably in its high contents of Ca-Tschermak's (CaTs) molecule (22 mol %) and Na2O (1.4 wt%). Clinopyroxene–melt partition coefficients (D) for a wide range of trace elements, determined by SIMS analysis of run products, differ markedly from those reported in other studies under conditions less appropriate to mantle melting. In particular partition coefficients for the heavy rare earth elements (Gd–Lu) are greater than unity (e.g. DLu=1.45), and the critical partitioning parameter, (DSm/DNd)×(DHf/DLu), is 0.68. These features, which arise due to the high CaTs content of the clinopyroxene, dramatically reduce the required involvement of garnet in the melting region beneath mid-ocean ridges. 相似文献
5.
Temporal evolution of the Mariana arc during rifting of the Mariana Trough traced through the volcaniclastic record 总被引：1，自引：0，他引：1
The sedimentary sequences that accumulate around volcanic arcs may be used to reconstruct the history of volcanism provided the degree of along-margin sediment transport is modest, and that reworking of old sedimentary or volcanic sequences does not contribute substantially to the sediment record. In the Mariana arc, the rare earth and trace element compositions of ash layers sampled by Deep Sea Drilling Project (DSDP) site 451 on the West Mariana Ridge, and sites 458 and 459 on the Mariana Forearc, were used to reconstruct the evolution of the arc volcanic front during rifting of the Mariana Trough. Ion microprobe analysis of individual glass shards from the sediments shows that the glasses have slightly light rare earth element (LREE)-enriched compositions, and trace element compositions typical of arc tholeiites. The B/Be ratio is a measure of the involvement of subducted sediment in petrogenesis, and is unaffected by fractional crystallization. This ratio is variable over the period of rifting, increasing up-section at site 451 and reaching a maximum in sediments dated at 3–4 Ma, ∼ 3–4 million years after rifting began. This may reflect increased sediment subduction during early rifting and roll-back of the Pacific lithosphere. Parallel trends are not seen in the enrichment of incompatible high field strength (HFSE), large ion lithophile (LILE) or rare earth elements (REE), suggesting that flux from the subducting slab alone does not control the degree of melting. Re-establishment of arc volcanism on the trench side of the basin at ca 3 Ma resulted in volcanism with relative enrichment in incompatible REE, HFSE and LILE, although these became more depleted with time, possibly due to melt extraction from the mantle source as it passed under the developing back-arc spreading axis, prior to melting under the volcanic front. 相似文献
6.
Abstract Spinel lherzolite is a minor component of the deep-seated xenolith suite in the Oki-Dogo alkaline basalts, whereas other types of ultramafic (e.g. pyroxenite and dunite) and mafic (e.g. granulite and gabbro) xenoliths are abundant. All spinel lherzolite xenoliths have spinel with a low Cr number (Cr#; < 0.26). They are anhydrous and are free of modal metasomatism. Their mineral assemblages and microtextures, combined with the high NiO content in olivine, suggest that they are of residual origin. But the Mg numbers of silicate minerals are lower (e.g. down to Fo86 ) in some spinel lherzolites than in typical upper mantle residual peridotites. The clinopyroxene in the spinel lherzolite shows U-shaped chondrite-normalized rare-earth element (REE) patterns. The abundance of Fe-rich ultramafic and mafic cumulate xenoliths in Oki-Dogo alkali basalts suggests that the later formation of those Fe-rich cumulates from alkaline magma was the cause of Fe- and light REE (LREE)-enrichment in residual peridotite. The similar REE patterns are observed in spinel peridotite xenoliths from Kurose and also in those from the South-west Japan arc, which are non-metasomatized in terms of major-element chemistry (e.g. Fo > 89), and are rarely associated with Fe-rich cumulus mafic and ultramafic xenoliths. This indicates that the LREE-enrichment in mantle rocks has been more prominent and prevalent than Fe and other major-element enrichment during the metasomatism. 相似文献
7.
The Oligocene alkaline basalts of Toveireh area (southwest of Jandaq, Central Iran) exhibit northwest–southeast to west–east exposure in northwest of the central‐east Iranian microcontinent (CEIM). These basalts are composed of olivine (Fo70–90), clinopyroxene (diopside, augite), plagioclase (labradorite), spinel, and titanomagnetite as primary minerals and serpentine and zeolite as secondary ones. They are enriched in alkalis, TiO2 and light rare earth elements (La/Yb = 9.64–12.68) and are characterized by enrichment in large ion lithophile elements (Cs, Rb, Ba) and high field strength elements (Nb, Ta). The geochemical features of the rocks suggest that the Toveireh alkaline basalts are derived from a moderate degree partial melting (10–20%) of a previously enriched garnet lherzolite of asthenospheric mantle. Subduction of the CEIM confining oceanic crust from the Triassic to Eocene is the reason of mantle enrichment. The studied basalts contain mafic‐ultramafic and aluminous granulitic xenoliths. The rock‐forming minerals of the mafic‐ultramafic xenoliths are Cr‐free/poor spinel, olivine, Al‐rich pyroxene, and feldspar. The aluminous granulitic xenoliths consist of an assemblage of hercynitic spinel + plagioclase (andesine–labradorite) ± corundum ± sillimanite. They show interstitial texture, which is consistent with granulite facies. They are enriched in high field strength elements (Ti, Nb and Ta), light rare earth elements (La/Yb = 37–193) and exhibit a positive Eu anomaly. These granulitic xenoliths may be Al‐saturated but Si‐undersaturated feldspar bearing restitic materials of the lower crust. The Oligocene Toveireh basaltic magma passed and entrained these xenoliths from the lower crust to the surface. 相似文献
8.
《Acta Geochimica》2017,(1)
Harrat Al-Birk volcanics are products of the Red Sea rift in southwest Saudi Arabia that started in the Tertiary and reached its climax at ~ 5 Ma.This volcanic field is almost monotonous and is dominated by basalts that include mafic-ultramafic mantle xenoliths(gabbro,websterite,and garnet-clinopyroxenite).The present work presents the first detailed petrographic and geochemical notes about the basalts.They comprise vesicular basalt,porphyritic basalt,and flow-textured basalt,in addition to red and black scoria.Geochemically,the volcanic rock varieties of the Harrat Al-Birk are low- to medium-Ti,sodic-alkaline olivine basalts with an enriched oceanic island signature but extruded in a within-plate environment.There is evidence of formation by partial melting with a sort of crystal fractionation dominated by clinopyroxene and Fe-Ti oxides.The latter have abundant titanomagnetite and lesser ilmenite.There is a remarkable enrichment of light rare earth elements and depletion in Ba,Th and K,Ta,and Ti.The geochemical data in this work suggest Harrat Al-Birk basalts represent products of watersaturated melt that was silica undersaturated.This melt was brought to the surface through partial melting of asthenospheric upper mantle that produced enriched oceanic island basalts.Such partial melting is the result of subducted continental mantle lithosphere with considerable mantle metasomatism of subducted oceanic lithosphere that might contain hydrous phases in its peridotites.The fractional crystallization process was controlled by significant separation of clinopyroxene followed by amphiboles and Fe-Ti oxides,particularly ilmenite.Accordingly,the Harrat Al-Birk alkali basalts underwent crystal fractionation that is completely absent in the exotic mantle xenoliths(e.g.Nemeth et al.in The Pleistocene Jabal Akwa A1 Yamaniah maar/tuff ring-scoria cone complex as an analogy for future phreatomagmatic to magmatic explosive eruption scenarios in the Jizan Region,SW Saudi Arabia 2014). 相似文献
9.
Abstract The Isabela ophiolite, the Philippines, is characterized by a lherzolite‐dominant mantle section, which was probably formed beneath a slow‐spreading mid‐ocean ridge. Several podiform chromitites occur in the mantle section and grade into harzburgite to lherzolite. The chromitites show massive, nodular, layered and disseminated textures. Clinopyroxene (±orthopyroxene/amphibole) inclusions within chromian spinel (chromite hereafter) are commonly found in the massive‐type chromitites. Large chromitites are found in relatively depleted harzburgite hosts having high‐Cr? (Cr/(Cr + Al) atomic ratio = ～0.5) chromite. Light rare earth element (LREE) contents of clinopyroxenes in harzburgites near the chromitites are higher than those in lherzolite with low‐Cr? chromite, whereas heavy REE (HREE) contents of clinopyroxenes are lower in harzburgite than in lherzolite. The harzburgite near the chromitites is not a residual peridotite after simple melt extraction from lherzolite but is formed by open‐system melting (partial melting associated with influx of primitive basaltic melt of deeper origin). Clinopyroxene inclusions within chromite in chromitites exhibit convex‐shaped REE patterns with low HREE and high LREE (+Sr) abundances compared to the host peridotites. The chromitites were formed from a hybridized melt enriched with Cr, Si and incompatible elements (Na, LREE, Sr and H2O). The melt was produced by mixing of secondary melts after melt–rock interaction and the primitive basaltic melts in large melt conduits, probably coupled with a zone‐refining effect. The Cr? of chromites in the chromitites ranges from 0.65 to 0.75 and is similar to those of arc‐related magmas. The upper mantle section of the Isabela ophiolite was initially formed beneath a slow‐spreading mid‐ocean ridge, later introduced by arc‐related magmatisms in response to a switch in tectonic setting during its obduction at a convergent margin. 相似文献
10.
Petrogenesis of basalts from the FAMOUS area: Mid-Atlantic Ridge 总被引：1，自引：0，他引：1
C.H. Langmuir J.F. Bender A.E. Bence G.N. Hanson S.R. Taylor 《Earth and Planetary Science Letters》1977,36(1):133-156
Fresh basalt glasses most of which have Mg/(Mg + Fe2+) of 0.66–0.72 from outcrops within 3 km of one other in the rift valley at the Project FAMOUS locality have been analyzed for major, minor and trace elements in order to determine their petrogenesis.Transition metal abundances of the FAMOUS samples are similar to a wide variety of continental and oceanic basalts with high MgO and Ni, all of which show remarkably little variation, with the exception of Cu, Zn and Ti, on a chondrite-normalized plot. Modelling of these data suggests that the mantle beneath both continents and oceans is systematically fractionated relative to chondrites. This fractionation provides a constraint for models of earth formation and subsequent evolution.The abundances of the rare earth and the incompatible elements, Ba, La, Th, U, and Nb, vary by more than a factor of three and the La/Yb and La/Sm ratios vary by factors of 3.1 and 1.6, respectively, in samples with similar, high Mg/(Mg + Fe2+). There is no correlation between the degree of light-REE enrichment and the heavy-REE abundance. Furthermore, the trace element variations do not appear correlated with respect to location in the rift valley or to time of eruption. These trace element features demonstrate that successive eruptions in one small area of the rift valley can show wide variations in trace element chemistry over a short span of time; they preclude the derivation of these basalt glasses from a single magma chamber.Despite the heterogeneities in REE and the variable trace element abundances, a homogeneous mantle source is suggested by the similarities among the samples in the incompatible element ratios of La/Ce, Ba/Th, Zr/Nb and K/Ba and the small range in87Sr/86Sr isotope ratios observed in other samples from the FAMOUS region (White and Bryan, 1977). Thus, trace element heterogeneities appear to be generated by processes in the mantle during melting. However, processes such as batch partial melting, fractional fusion, fractional crystallization, zone refining, or mixing of magmas or sources acting alone are incapable of explaining the lack of correlation between the light and heavy REE.It is suggested that the observed variations are a consequence of dynamic partial melting of a homogeneous mantle source region. This process includes varying degrees of partial melting of an uprising mantle source with continuous but incomplete removal of melt as melting proceeds, varying extents of batch partial melting, and zone refining. Dynamic melting can produce different melts from a homogeneous source which have different degrees of light-REE enrichment and crossing REE patterns. The variable trace element abundances which may be produced through dynamic melting may be the cause of the apparent decoupling of major and trace elements (Bryan et al., 1976) which previously has been suggested for the FAMOUS region (Bryan and Moore, 1977). 相似文献
11.
Geothermal gradient of the upper mantle beneath Jeju Island, Korea: Evidence from mantle xenoliths 总被引：2，自引：0，他引：2
Abstract Ultramafic xenoliths found in alkali basalts from Jeju Island, Korea are mostly spinel lherzolites accompanied by subordinate amount of spinel harzburgites and pyroxenites. The combination of results from a two-pyroxene geothermometer and Ca-in-olivine geobarometer yields temperature–pressure (T–P) estimates for spinel peridotites that fall in experimentally determined spinel lherzolite field in CaO-Fe-MgO-Al2 O3 -SiO2 -Cr2 O3 (CFMASCr) system. These T–P data sets have been used to construct the Quaternary Jeju Island geotherm, which defines a locus from about 13 kbar at 880°C to 26 kbar at 1040°C. The geothermal gradient of Jeju Island is greater than that of the conventional conductive models, and may be as a result of a thermal perturbation by the heat input into the lithospheric mantle via the passage and emplacement of magma. Spinel–lherzolite is the main constituent rock-type of the lithospheric mantle beneath Jeju Island. Pyroxenites may be intercalated in peridotites at similar depth and temperature as re-equilibrated veins or lenses. 相似文献
12.
Clinopyroxenes separated from two hydrous and four anhydrous ultramafic nodules, selected from a suit of xenoliths from Dreiser Weiher (DW), West Germany, have been studied for Nd and Sr isotopic composition. Nd exhibits a range of εJUV(T) from 0 to +12.4 and 87Sr/86Sr varies between 0.70185 and 0.70400. TICE model ages for anhydrous nodules indicate that the mantle underlying DW was originally depleted ?2 AE ago. Correlation of 143Nd/144Nd with Sm/Nd in this group of samples suggests that a second partial melting event occurred about 560 m.y. ago resulting in LREE enrichment of at least part of the anhydrous mantle. During a later episode, probably contemporaneous with the eruption of the host basalt in Quaternary times, most of the spinel peridotitic upper mantle below DW was modified. This metasomatism led to hydration and incompatible element enrichment of originally anhydrous mantle. The isotopic data for the anhydrous nodules again demonstrate that oceanic-type mantle underlies at least some continental areas. It is apparent that the separation of subcontinental mantle regions from an initially chondritic reservoir may occur in several discrete episodes. However, differing histories of depletion and/or enrichment will produce isotopically distinct mantle reservoirs. Therefore, basalts extracted from these mantle reservoirs will scatter about an average Nd-Sr trend line reflecting the nature of the differentiation in their source regions. 相似文献
13.
Alexey Y. Martynov Jun-Ichi Kimura Yuri A. Martynov Alexsander V. Rybin 《Island Arc》2010,19(1):86-104
Middle Miocene to Quaternary lavas on Kunashir Island in the southern zone of the Kurile Arc were examined for major, trace, and Sr–Nd–Pb isotope compositions. The lavas range from basalt through to rhyolite and the mafic lavas show typical oceanic island arc signatures without significant crustal or sub-continental lithosphere contamination. The lavas exhibit across-arc variation, with increasingly greater fluid-immobile incompatible element contents from the volcanic front to the rear-arc; this pattern, however, does not apply to some other incompatible elements such as B, Sb, and halogens. All Sr–Nd–Pb isotope compositions reflect a depleted source with Indian Ocean mantle domain characteristics. The Nd and Pb isotope ratios are radiogenic in the volcanic front, whereas Sr isotope ratios are less radiogenic. These Nd isotope ratios covary with incompatible element ratios such as Th/Nd and Nb/Zr, indicating involvement of a slab-derived sediment component by addition of melt or supercritical fluid capable of mobilizing these high field-strength elements and rare earth elements from the slab. Fluid mobile elements, such as Ba, are also elevated in all basalt suites, suggesting involvement of slab fluid derived from altered oceanic crust. The Kurile Arc lavas are thus affected both by slab sediment and altered basaltic crust components. This magma plumbing system has been continuously active from the Middle Miocene to the present. 相似文献
14.
Petrogenesis of diabase from accretionary prism in the southern Qiangtang terrane,central Tibet: Evidence from U–Pb geochronology,petrochemistry and Sr–Nd–Hf–O isotope characteristics 
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下载免费PDF全文 The Bangong–Nujiang suture (BNS) between the Lhasa and Qiangtang terranes is an important boundary and its petrogenesis is controversial. Diabase from the accretionary prism in the southern Qiangtang terrane yields a zircon U–Pb age of 181.3 ± 1.4 Ma. All the diabases show tholeiitic basalt compositions, gentle enrichment patters of light rare earth elements (REE), variable enrichment in incompatible element concentrations (e.g. Th and Rb), and no anomaly in high field strength elements (e.g. Nb and Ta), similar to that of enriched mid‐ocean ridge basalt (E‐MORB). They have relatively homogeneous whole rock Nd (εNd(t) = 7.3–9.1) and zircon Hf–O isotopic compositions (εHf(t) = 14.8–16.1, and δ18O = 4.57–6.12‰), possibly indicating melting of the depleted mantle and no significant crustal contamination during the petrogenesis. The element variations suggest that the diabases were formed by plume–ridge interaction at a mid‐ocean ridge within the Bangong–Nujiang ocean. 相似文献
15.
Selected basalts from a suite of dredged and drilled samples (IPOD sites 525, 527, 528 and 530) from the Walvis Ridge have been analysed to determine their rare earth element (REE) contents in order to investigate the origin and evolution of this major structural feature in the South Atlantic Ocean. All of the samples show a high degree of light rare earth element (LREE) enrichment, quite unlike the flat or depleted patterns normally observed for normal mid-ocean ridge basalts (MORBs). Basalts from Sites 527, 528 and 530 show REE patterns characterised by an arcuate shape and relatively low (Ce/Yb)N ratios (1.46–5.22), and the ratios show a positive linear relationship to Nb content. A different trend is exhibited by the dredged basalts and the basalts from Site 525, and their REE patterns have a fairly constant slope, and higher (Ce/Yb)N ratios (4.31–8.50).These differences are further reflected in the ratios of incompatible trace elements, which also indicate considerable variations within the groups. Mixing hyperbolae for these ratios suggest that simple magma mixing between a “hot spot” type of magma, similar to present-day volcanics of Tristan da Cunha, and a depleted source, possibly similar to that for magmas being erupted at the Mid-Atlantic Ridge, was an important process in the origin of parts of the Walvis Ridge, as exemplified by Sites 527, 528 and 530. Site 525 and dredged basalts cannot be explained by this mixing process, and their incompatible element ratios suggest either a mantle source of a different composition or some complexity to the mixing process. In addition, the occurrence of different types of basalt at the same location suggests there is vertical zonation within the volcanic pile, with the later erupted basalts becoming more alkaline and more enriched in incompatible elements.The model proposed for the origin and evolution of the Walvis Ridge involves an initial stage of eruption in which the magma was essentially a mixture of enriched and depleted end-member sources, with the N-MORB component being small. The dredged basalts and Site 525, which represent either later-stage eruptives or those close to the hot spot plume, probably result from mixing of the enriched mantle source with variable amounts and variable low degrees of partial melting of the depleted mantle source. As the volcano leaves the hot spot, these late-stage eruptives continue for some time. The change from tholeiitic to alkalic volcanism is probably related either to evolution in the plumbing system and magma chamber of the individual volcano, or to changes in the depth of origin of the enriched mantle source melt, similar to processes in Hawaiian volcanoes. 相似文献
16.
Huronian basalts from central Ontario, Canada, dated at about 2450 Ma and associated with an early rifting episode, are classified as siliceous, low-TiNb tholeiites. They display strong enrichment in large-ion lithophile (LILE) and light rare earth (LREE) elements compared to modern oceanic lavas. The tectonic setting and geochemistry resemble Mesozoic rift-related low-Ti flood basalts, including the Ferrar Group of Antarctica, and the Parana and equivalent Etendeka volcanics of south Brazil and Namibia, respectively. High LILE/LREE ratios are also similar to subduction-related island arc tholeiites, and it is suggested that enrichment of the Huronian lithospheric mantle source occurred through ancient subduction of crustal material, probably during formation and consolidation of the Archean continental crust.Melting models suggest that Huronian subcontinental mantle source compositions, derived from least contaminated, aphyric, mafic end-members, had already undergone a complex evolution, including withdrawal of Archean basalts and hydrous enrichment in incompatible components. Despite several subsequent melting episodes and a second, probably magmatic, enrichment event, however, many aspects of the Huronian source signature were preserved, and appeared in later basaltic products of this mantle mass. Keweenawan volcanics, for example, dated at about 1100 Ma, preserve low P, Zr, Ti and HREE abundances. 相似文献
17.
Y S O’Reilly 《中国科学D辑(英文版)》2006,49(9):926-937
The partial melting and metasomatism are two most important geological processes of changing chemical compositions of mantle. Extracting partial melt from primitive mantle leads residual mantle to deplete in- compatible elements, whereas the metasomatism … 相似文献
18.
Abstract The mantle-derived xenoliths entrained in the Pliocene basanite from Baengnyeong Island, South Korea, are spinel lherzolites and spinel harzburgites. The overall compositional range of the Baengnyeong xenoliths matches that of the post-Archean xenoliths of lithospheric mantle origin from eastern China, but without any compositional evidence for a refractory Archean mantle root. Mineral compositions of the xenoliths have been used to estimate the equilibrium temperatures and pressures, and to construct a paleogeothermal gradient of the source region. The xenolith-derived paleogeotherm is constrained from about 820°C at 7.3 kbar to 1000°C at 20.6 kbar. Like those from the post-Archean Chinese xenoliths of lithospheric mantle origin, the Baengnyeong geotherm is considerably elevated relative to the conductive models at the depth of the crust–mantle boundary, reflecting a thermal perturbation probably related to lithospheric thinning. There is no significant P / T difference between harzburgite and lherzolite, which suggests that the harzburgites are interlayered with lherzolites within the depth interval beneath Baengnyeong Island. 相似文献
19.
Peter B. Kelemen Nobumichi Shimizu Todd Dunn 《Earth and Planetary Science Letters》1993,120(3-4):111-134
Depletion of Nb relative to K and La is characteristic of lavas in subduction-related magmatic arcs, as distinct from mid-ocean ridge basalts. Nb depletion is also characteristic of the continental crust. This and other geochemical similarities between the continental crust and high-Mg# andesite magmas found in arcs suggests that the continental crust may have formed by accretion of andesites. Previous studies have shown that the major element characteristics of high-Mg# andesites may be produced by melt/rock reaction in the upper mantle. In this paper, new data on partitioning of K, Nb, La and Ce between garnet, orthopyroxene and clinopyroxene in mantle xenoliths, and on partitioning of Nb and La between orthopyroxene and liquid, show that garnet and orthopyroxene have Nb crystal/liquid distribution coefficients which are much larger than those of K and La. Similar fractionations of Nb from K and La are expected in spinel and olivine. For this reason, reactions between migrating melt and large masses of mantle peridotite can produce substantial depletion of Nb in derivative liquids. Modeling shows that reaction between ascending, mantle-derived melts and mantle peridotite is a viable mechanism for producing the trace element characteristics of high-Mg# andesite magmas and the continental crust.
Alternatively, small-degree melts of metabasalt and/or metasediment in the subducting slab may leave rutile in their residue, and will thus have large Nb depletions relative to K and La [1]. Slab melts are too rich in light rare earth elements and other incompatible elements, and too poor in compatible elements, to be parental to arc magmas. However, ascending slab melts may be modified by reaction with the mantle. Our new data permit modeling of the trace element effects of reaction between small-degree melts of the slab and mantle peridotite. Modeling shows that this type of reaction is also a viable mechanism for producing the trace element characteristics of high-Mg# andesites and the continental crust. These findings, in combination with previous results, suggest that melt/rock reaction in the upper mantle has been an important process in forming the continental crust and mantle lithosphere. 相似文献
20.
Os isotope ratios of mantle peridotites have been considered to be largely immune to recent melt-rock interaction. However, Os isotope ratios and PGE (Platinum group elements) concentrations of the Yong’an xenoliths have been significantly modified by melt percolation, and are not suitable for determining the formation age of lithosphere mantle in Yong’an. In this study, the Yong’an spinel peridotite xenoliths are divided into two groups: N-Type and E-Type. The N-Type group including cpx (clinopyroxene)-poor lherzolite and harzburgite, shows a large variation of Cr#(sp) (13.2-48) and sulfur contents (from 171 ppm to below detection limit), whereas the E-Type peridotites are mainly refractory harzburgites and are characterized by high Cr#(sp) (35.3-42.2) and overall low sulfur contents (below 51 ppm). Both types show similar major and REE (rare earth element) patterns. Furthermore, the N-Type peridotites display a restricted range of iridium-group PGE (IPGE), Os/Ir and Ru/Ir ratios (Os/Ir = 0.64-1.12, Ru/Ir = 1.52-1.79) and variable palladium-group PGE (PPGE) contents (3.4-14.9 ppb), whereas the E-Type peridotites show a large variation of Os/Ir and Ru/Ir ratios (Os/Ir = 0.33-0.84, Ru/Ir = 0.94-1.6), and a restricted range of PPGE (4.3-6.9 ppb). 187Os/188Os ratios of E-Type peridotites are higher than those of N-Type peridotites at comparable fertility levels. These results suggest that N-Type peridotites may have been overprinted by metasomatism via small melt fractions, in which the percolation of the volatile-rich, small melt fractions only resulted in LILE (large ion lithophile element) enrichment of clinopyroxene, and their whole rock PGE contents and Re-Os isotope values were little changed. Moreover, E-Type peridotites may have been modified by melt-rock reaction involving relatively large melt fractions, which may result in the formation of secondary cpx and olivine and the removal of IPGE-bearing minerals such as Ru-Os-(Ir) alloys or laurite, followed by precipitation of secondary sulfides from melt with radiogenic isotopic signature. 相似文献