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1.
Geochemistry of the Hawi lavas,Kohala Volcano,Hawaii   总被引：1，自引：0，他引：1  
Hawi lavas form the late stage alkalic cap on Kohala Volcano and range in composition from hawaiite to trachyte. New, detailed field mapping of Kohala and reinterpretation of previously published age data suggest that there was no significant eruption hiatus between the Hawi and underlying Pololu shield lavas as was previously suggested. Mineral and whole-rock chemical data are consistent with a crystal fractionation origin for the hawaiite to trachyte compositional variation observed within the Hawi lavas. Plagioclase, clinopyroxene, Ti-magnetite, olivine and apatite fractionation are needed to explain this variation. The clinopyroxene fractionation may have occurred at moderate pressure because it is virtually absent in these lavas and is not a near liquidus phase at pressures of less than 8 Kb. Plagioclase would be buoyant in the Hawi hawaiite magmas so a mechanism like dynamic flow crystallization is needed for its fractionation and to account for the virtual absence of phenocrysts in the lavas. Hawi lavas are distinct in Sr and Nd isotopic ratios and/or incompatible element ratios from the Pololu lavas. Thus they were derived from compositionally distinct sources. Compared to other suites of Hawaiian alkalic cap lavas, Hawi lavas have anomalously high concentrations of phosphorus and rare earth elements. These differences could be due to greater apatite content in the source for the Hawi lavas.  相似文献   

2.
As technical advances have dramatically increased our ability to analyze trace elements, the need for more reliable data on the compositional dependence of trace element partitioning between minerals and melt has become increasingly important. The late-Cretaceous Carmacks Group of south central Yukon comprises a succession of primitive high-Mg ankaramitic lavas characterized by shoshonitic chemical affinities and containing large complexly zoned clinopyroxene phenocrysts. The compositional zonation of the clinopyroxene phenocrysts is characterized by relatively Fe-rich (Mg# = Mg/(Mg + Fe) = 0.85), but mottled, cores surrounded by mantles of cyclically-zoned clinopyroxene whose Mg# varies repeatedly between 0.9 and 0.80. These cyclically zoned clinopyroxene mantles appear to record the repeated influx and mixing of batches of primitive with more evolved magma in a deep sub-crustal (∼1.2 GPa) magma chamber(s). Laser ablation ICP-MS was used to analyze the trace element variation in these zoned clinopyroxenes. The results indicate more than a threefold variation in the absolute concentrations of Th, Zr, rare earth elements (REE), and Y within individual clinopyroxene phenocrysts, with no apparent change in the degree of REE or high field strength element (HFSE) fractionation. The variation in absolute abundances of trace elements correlates closely with the major element composition of the clinopyroxene, with the most enriched clinopyroxene having the lowest Mg# and highest Al contents. The problem is that the amount of crystal fractionation required to explain the major element variation (∼20%) in these clinopyroxene phenocrysts cannot explain the increase in the abundance of the incompatible trace elements, which would require more than 70% crystal fractionation, if constant partition coefficients are assumed. The anomalous increase in incompatible trace elements appears to reflect an increase in their partition coefficients with increasing AlIV in the clinopyroxene; with an increase in Al2O3 from 1.5 to 4.0 wt.% during ∼20% crystal fractionation over a temperature decrease of ∼100°C being associated with more that a threefold increase in the partition coefficients of Th, Zr, REE, and Y. The magnitude of these increases may indicate that the substitution of these trace elements into clinopyroxene is better modeled in some natural systems by a local charge balance model, rather than the distributed charge model that better replicates the results of annealed experiments. These findings indicate that the effect of Al on the partition coefficients of incompatible trace elements in clinopyroxene may be under appreciated in natural magmatic systems and that the application of experimentally determined clinopyroxene partition coefficients to natural systems must be done with caution.  相似文献   

3.
Mineralogical, major and trace element, and isotopic data are presented for leucite basanite and leucite tephrite eruptives and dykes from the Batu Tara volcano, eastern Sunda arc. In general, the eruptives are markedly porphyritic with phenocrysts of clinopyroxene, olivine, leucite ±plagioclase±biotite set in similar groundmass assemblages. These K-rich alkaline volcanics have high concentrations of large-ion-lithophile (LIL), light rare earth (LRE) and most incompatible trace elements, and are characterized by high 87Sr/86Sr (0.70571–0.70706) and low 143Nd/ 144Nd (0.512609–0.512450) compared with less alkaline volcanics from the Sunda arc. They also display the relative depletion of Ti and Nb in chondrite-normalized plots which is a feature of subalkaline volcanics from the eastern Sunda arc and arc volcanics in general. Chemical and mineralogical data for the Batu Tara K-rich rocks indicate that they were formed by the accumulation of variable amounts of phenocrysts in several melts with different major and trace element compositions. The compositions of one of these melts estimated from glass inclusions in phenocrysts is relatively Fe-rich (100 Mg/(Mg + Fe2+)=48–51) and is inferred to have been derived from a more primitive magma by low-pressure crystal fractionation involving olivine, clinopyroxene and spinel. Mg-rich (mg 90) and Cr-rich (up to 1.7 wt. % Cr2O3) zones in complex oscillatory-zoned clinopyroxene phenocrysts probably also crystallized from such a magma. The marked oscillatory zoning in the clinopyroxene phenocrysts is considered to be the result of limited mixing of relatively evolved with more primitive magmas, together with their phenocrysts, along interfaces between discrete convecting magma bodies.  相似文献   

4.
Iron isotope and major- and minor-element compositions of coexisting olivine, clinopyroxene, and orthopyroxene from eight spinel peridotite mantle xenoliths; olivine, magnetite, amphibole, and biotite from four andesitic volcanic rocks; and garnet and clinopyroxene from seven garnet peridotite and eclogites have been measured to evaluate if inter-mineral Fe isotope fractionation occurs in high-temperature igneous and metamorphic minerals and if isotopic fractionation is related to equilibrium Fe isotope partitioning or a result of open-system behavior. There is no measurable fractionation between silicate minerals and magnetite in andesitic volcanic rocks, nor between olivine and orthopyroxene in spinel peridotite mantle xenoliths. There are some inter-mineral differences (up to 0.2‰ in 56Fe/54Fe) in the Fe isotope composition of coexisting olivine and clinopyroxene in spinel peridotites. The Fe isotope fractionation observed between clinopyroxene and olivine appears to be a result of open-system behavior based on a positive correlation between the Δ56Feclinopyroxene-olivine fractionation and the δ56Fe value of clinopyroxene and olivine. There is also a significant difference in the isotopic compositions of garnet and clinopyroxene in garnet peridotites and eclogites, where the average Δ56Feclinopyroxene-garnet fractionation is +0.32 ± 0.07‰ for six of the seven samples. The one sample that has a lower Δ56Feclinopyroxene-garnet fractionation of 0.08‰ has a low Ca content in garnet, which may reflect some crystal chemical control on Fe isotope fractionation. The Fe isotope variability in mantle-derived minerals is interpreted to reflect subduction of isotopically variable oceanic crust, followed by transport through metasomatic fluids. Isotopic variability in the mantle might also occur during crystal fractionation of basaltic magmas within the mantle if garnet is a liquidus phase. The isotopic variations in the mantle are apparently homogenized during melting processes, producing homogenous Fe isotope compositions during crust formation.  相似文献   

5.
刘鑫  汤艳杰 《岩石学报》2018,34(11):3315-3326
冀西北姚家庄存在一套晚三叠世的超镁铁岩-正长岩杂岩体,岩体内发育具有环带特征的单斜辉石。辉石的环带有两种:简单环带和复杂环带。简单环带一般为正环带,辉石核部的MgO和Cr2O3含量高,Si O2、Fe O和Na2O含量低;边部的主要氧化物含量与核部刚好相反。简单正环带可以分为两类,其中核边接触带平滑、由核到边化学成分具有渐变特征的正环带辉石可能是岩浆在分离结晶或地壳混染过程中形成。而核边接触带有熔蚀结构、由核到边化学成分突变的正环带辉石可能是早期结晶的辉石颗粒受到晚期低镁岩浆的溶蚀改造而成的。复杂环带具有核-幔-边结构,其中,核部低镁高铁、幔部高镁低铁、边部与核部相似,但其Mg#更低,这些特征暗示了岩浆混合作用的存在,形成辉石核部的母岩浆可能来自富集的岩石圈地幔,幔部高Mg#的特征指示了软流圈地幔物质的贡献,其边部低Mg#的特征则指示了地壳物质的加入。具有韵律环带的复杂辉石是在岩浆多期侵入的过程中形成的。辉石环带的组成特征表明,姚家庄杂岩体是由岩浆多期侵位形成的,后期侵入的岩浆与前期就位的岩浆不断反应,形成了具有多种不同环带特征的辉石,并最终形成了空间上由外到内依次为辉石岩、辉石正长岩和正长岩的环状杂岩体。结合前人的研究成果,推测形成姚家庄岩体的岩浆主要来源于富集的岩石圈地幔,并由少量地壳组分和软流圈物质的贡献。  相似文献   

6.
Detailed chemical and mineralogical data are given for three sequences of basalts and picrite basalts from bore-holes in Western India. The picrite basalts show bulk compositional variation generated by the fractionation of olivine and chromite. Evolved picrite basalt magma appears to have given rise to basalt by the fractionation of olivine+clinopyroxene, despite the presence of abundant plagioclase phenocrysts. It is suggested that a slow settling rate for plagioclase relative to clinopyroxene and olivine is sufficient to account for this feature. The high degree of equilibrium crystallisation which many of the lavas have apparently undergone is interpreted in terms of the mechanism of compensated crystal settling (Cox and Bell, 1972). Experimentally determined atmospheric pressure phase relations are used to model dyke-like magma chambers in some detail. Finally volumetric and age relationships are used to argue that the picrite basalts, despite their porphyritic nature, crystallised from ultramafic liquids containing in some cases at least 16% MgO.  相似文献   

7.
Andesites of the calc-alkaline volcanic series associated with the circum-Pacific orogenic zone commonly contain crystal clots consisting essentially of plagioclase, clinopyroxene, orthopyroxene, and magnetite. It is proposed that these crystal clots represent the breakdown products of an amphibole as it enters the low-pressure environment of the upper crust. The bulk chemical composition of the clots compares favorably to that of the high-Al amphibole, pargasitic hornblende. The crystal clots support the hypothesis of the formation of andesitic magma by fractionation of early formed amphibole from a basaltic magma at total pressures less than 18 kbars and temperatures less than 1000° C. The origin of these clots has previously been attributed to random accumulation of phenocrysts. Some features of clot-bearing andesites from Crater Lake, Oregon, U.S.A., cannot be explained by this mechanism. First, in some andesites, certain minerals occur as phenocrysts but are not constituents of the clots, and conversely, certain minerals occurring as accessories in the clots are rarely found as phenocrysts. Second, the minerals comprising the clots occur in a fixed ratio that is significantly different than the ratio of the same minerals as phenocrysts. Crystal clots may form up to 10% by volume of the andesite, imparting a glomeroporphyritic texture to the rock. Crystal clots can be distinguished from xenoliths of similar mineralogy by the presence in the latter of abundant glass, both as interstitial material and as inclusions in the plagioclase grains, giving the plagioclase a “spongy” appearance.  相似文献   

8.
Melting experiments carried out at 1-atm and at 2 kbar on mid-ocean ridge basalts dredged from the mid-Atlantic ridge near the Kane Fracture Zone (KFZ, 22° to 25° N. latitude) provide a basis for evaluating the role of crystal fractionation in generating compositional variability observed in normal mid-ocean ridge basalt. The 1-atm olivine-plagioclase-clinopyroxene saturation boundary for KFZ lavas defines a path in mineral projection schemes and in oxide-oxide diagrams that is displaced from the same experimentally determined boundaries in FAMOUS (Grove and Bryan 1983) and Oceanographer Fracture Zone (Walker et al. 1979) basalts. The glass margins of sparsely phyric KFZ lavas record small amounts of near surface, low pressure fractional crystallization, and their glass and bulk rock compositions are similar. An important signature of low pressure differentiation is recorded in the quenched glass margins of moderately phyric KFZ lavas compared to their bulk rock compositions, and the glass has evolved along low-pressure fractionation paths that are similar to those produced in the 1-atm experiments. Many of the lavas have retained phenocrysts in equilibrium proportions, so that their bulk rock compositions represent liquid compositions. When the effects of near-surface differentiation and crystal accumulation are removed from the Kane data set, and only liquid compositions are considered, a suite of basalt magmas can be identified that forms a trend in mineral component projection schemes parallel to the 1-atm oliv-plag-cpx multiple saturation boundary, but displaced from it toward olivine. These basalts have only olivine and plagioclase as phenocrysts, and are well removed from clinopyroxene saturation at low pressure. The compositional variation can not be generated by mixing any primary liquid composition with a low pressure liquid that has evolved along the oliv-plag-cpx multiple saturation boundary. Major and trace element models of this trend using olivine, plagioclase and clinopyroxene as fractionating phases match the compositional variability. This compositional trend is generated by fractionation at pressures greater than 2 kbar, but within the plagioclase stability field. A review of the data for other normal MORB suites from this part of the mid-Atlantic ridge reveals a similar elevated pressure fractionation signature which persists when the effects of low pressure magma mixing are removed from the data set.  相似文献   

9.
Mid-ocean ridge basalts (MORBs) from East Pacific Rise (EPR) 13°N are analysed for major and trace elements, both of which show a continuous evolving trend. Positive MgO-Al2O3 and negative MgO-Sc relationships manifest the cotectic crystallization of plagioclase and olivine, which exist with the presence of plagioclase and olivine phenocrysts and the absence of clinopyroxene phenocrysts. However, the fractionation of clinopyroxene is proven by the positive correlation of MgO and CaO. Thus, MORB samples are believed to show a "clinopyroxene paradox". The highest magnesium.bearing MORB sample E13-3B (MGO=9.52%) is modelled for isobaric crystallization with COMAGMAT at different pressures. Observed CaO/Al2O3 ratios can be derived from E13-3B only by fractional crystallization at pressure >4±1 kbar, which necessitates clinopyroxene crystallization and is not consistent with cotectic crystallization of olivine plus plagioclase in the magma chamber (at pressure～1 kbar). The initial compositions of the melt inclusions, which could represent potential parental magmas, are reconstructed by correcting for post-entrapment crystallization (PEC). The simulated crystallization of initial melt inclusions also produce observed CaO/Al2O3 ratios only at >4±1 kbar, in which clinopyroxene takes part in crystallization. It is suggested that MORB magmas have experienced clinopyroxene fractionation in the lower crust, in and below the Moho transition zone. The MORB magmas have experienced transition from clinopyroxene+plagioclase+olivine crystallization at >4±1 kbar to mainly olivine+plagioclase crystallization at <1 kbar, which contributes to the explanation of the "clinopyroxene paradox".  相似文献   

10.
Conclusion In summary, there are no existing clinopyroxene-liquid REE distribution data obtained under appropriate conditions to permit numerical modeling of trace elements to constitute a critical test of the pyroxene fractionation process. There are, however, numerous clinopyroxeneliquid partitioning data in the literature that give qualitatively similar patterns to those observed in grospydites. Further, the high pressure fractionation model accounts for the major-element and exsolution phenomena in a manner directly consistent with experimental petrologic studies, and can qualitatively account for the trace element and isotopic characteristics of the rocks in a manner consistent with the crystal chemistry of the phases. We therefore continue to prefer the high-pressure clinopyroxene fractionation model over a low-pressure plagioclase fractionation model for the origin of the grospydites.  相似文献   

11.
Petrographic, mineral chemical and whole-rock major oxide data are presented for the lavas of the Main Volcanic Series of Patmos, Dodecanesos, Greece. These lavas were erupted about 7 m.y. ago and range in composition from ne-trachybasalts through hy-trachybasalts and trachyandesites to Q-trachytes. To some extent, the ne-trachybasalts are intermediate in composition to the alkaline lavas found on oceanic islands and the calc-alkaline lavas of destructive plate margins. Major oxide variation is largely explicable in terms of fractional crystallization involving removal of the observed phenocryst and microphenocryst phases viz. olivine, plagioclase, clinopyroxene and Ti-magnetite in the mafic lavas, plagioclase, clinopyroxene, mica and Ti-magnetite in the evolved lavas. Apatite, which occurs as an inclusion in other phenocrysts or as microphenocrysts must also have been removed. However, mass balance calculations indicate that the chemistry of the hy-trachybasalts is inconsistent with an origin via fractional crystallization alone and the complex zoning patterns and resorbtion phenomena shown by phenocrysts in these lavas show that they are hybrids formed by the mixing of 80-77% ne-trachybasalt with 20–23% trachyandesite. It is estimated that the mixing event preceded eruption by a period of 12 h-2 weeks suggesting that mixing triggered eruption. Combined fractionation and mixing cannot explain the relatively low MgO contents of the hy-trachybasalts and it is concluded that assimilation also occurred. Assimilation, and especially addition of volatiles to the magmas, may be responsible for the evolutionary trend from ne-normative to hy-normative magmas and was probably facilitated by intensified convection resulting from mixing. A model is presented whereby primitive magma undergoes fractionation in an intracrustal magma chamber to yield more evolved liquids. Influx of hot primitive magma into the base of the chamber facilitates assimilation, but eventually mixing yields the hy-trachybasalts and finally the ne-trachybasalts are erupted.  相似文献   

12.
The Talasea Peninsula is composed of a chain of Quaternary volcanoes whose lavas range from basalt to rhyolite. The peninsula is situated in an orogenic environment and the lavas, while essentially calc-alkaline, show some differences from other orogenic suites on the Pacific rim. The most distinctive feature of the Talasea series is absolute iron enrichment in some lavas. Mineralogically, the andesites are characterized by phenocrysts of plagioclase, orthopyroxene, clinopyroxene and titanomagnetite, while the basalts lack titanomagnetite phenocrysts but contain olivine. The acid rocks have a mineralogy similar to that of the andesites, but also contain quartz, amphibole, biotite and ilmenite. The compositions of coexisting titanomagnetite and ilmenite in the acid lavas indicate equilibration temperatures in the range 920° to 860° C and oxygen fugacities ( ) above those of the fayalitemagnetite-quartz buffer assemblage. The mineralogical evidence supports the hypothesis of a crystal fractionation origin for this series and there is a possibility that the was more or less constant during the early stages of its evolution. The iron enriched lavas may be an offshoot from the main line of descent, resulting from near-surface fractionation, with the dominance of plagioclase in the crystal residuum producing an iron-rich liquid.  相似文献   

13.
Compositional relations among natural glasses in basalts recovered by Legs 45 and 46 (DSDP) provide powerful constraints on their differentiation histories. Residual glass compositions in the moderately evolved aphyric and abundantly phyric basalts within each site demonstrate that none of the units is mutually related to any other or to a common parent by simple fractional crystallization. At Site 396, where clinopyroxene phenocrysts are absent, progressively more evolved liquids (lower Mg/ (Mg+Fe) and higher TiO2) are characterized by lower calcium-aluminum ratios, which can only be generated by clinopyroxene fractionation. This paradox is amplified by some melt inclusions in olivine phenocrysts that have higher CaO/Al2O3 and lower TiO2 than any residual glasses. The occurrences of these distinctive compositions are correlated with the highly magnesian character of the host olivines (Fo90–89), and the melts are interpreted as trapped primitive liquids, parental to the more fractionated derivatives.Melt inclusions intermediate in composition between the residual glasses and the most primitive olivine melt inclusions are present in the cores of some plagioclase phenocrysts that have had a history of resorption. On the basis of a petrographic and microprobe analysis of the zoning relations in these phenocrysts, the inclusions are inferred to be melts entrapped at the time of extensive corrosion of the host crystals.Interpreted in conjunction with other mineral and geochemical data, the compositional trends in the glasses indicate that magma mixing has played a major role in the genesis of the Leg 45 and 46 basalts. The reality of mixing is demonstrated by extensive disequilibrium textures in the plagioclase phenocrysts and the presence in evolved lavas of refractory plagioclase and olivine phenocrysts bearing primitive melt inclusions. The chemical imprint of clinopyroxene fractionation despite the absence of clinopyroxene phenocrysts is believed to be accomplished by plating of gabbro on to the upper walls of the subvolcanic magma chamber as it evolves between mixing events. Repeated influxes of primitive magma batches will move the resultant hybrids alway from clinopyroxene saturation and generate olivine-plagioclase cotectic magmas. This model provides a physical buffering mechanism that accounts for the volumetric dominance of moderately evolved basalts among ocean floor tholeiites. Major and trace element models based on the combination of mixing and fractional crystallization also explain heretofore enigmatic geochemical characteristics of MORB.Lunar and Planetary Institute Contribution no. 326After August 1, 1978: Department of Geological Sciences, Southern Methodist University, Dallas, TX 75275, USAThe Lunar and Planetary Institute is operated by the Universities Space Research Association under Contract No. NSR 09-051-001 with the National Aeronautics and Space Administration  相似文献   

14.
A petrological and geochemical study of an olivine and of a clinipyroxene spinifex textured flow, from Alexo, indicates that the initial liquid in both flows probably came from the same mantle melting event and that the source was incompatible element depleted. The starting liquid of the clinopyroxene flow had experienced more olivine fractionation (10%) prior to its emplacement at Alexo, than the initial liquid of the olivine spinifex flow. The development of each of the textural and compositional zones in the flows can be modelled by means of crystal fractionation. In the case of the clinopyroxene flow the B-zone is formed by the fractionation of olivine, low-Ca pyroxene and chromite. An unusual feature of the Alexo clinopyroxene flow is presence of a peridotitic komatiite above the pyroxene cumulate layer, where a basaltic komatiite would usually be present. The presence of the peridotitic komatiite suggests an influx of new magma and hence a dynamic model for the flow. The composition of the clinopyroxene spinifex zone represents a mixture of clinopyroxene plus liquid, rather than simply a frozen liquid. This could happen if the clinopyroxene needles grew stalactitelike from the chilled upper surface of the flow into a flowing basaltic liquid. In the olivine spinifex flow the zones can be modelled as frozen liquids in the A2-zone, as initial liquid which has fractionated 30% olivine in the A3-zone and as liquid plus 50% olivine in the B-zone. But, if the clinopyroxene spinifex developed by stalactite growth of clinopyroxene needles into the a flowing liquid, the possibility that the olivine spinifex represent fractionated liquid plus stalactite olivines arises.  相似文献   

15.
Mid-ocean ridge basalts (MORBs) from East Pacific Rise (EPR) 13°N are analysed for major and trace elements, both of which show a continuous evolving trend. Positive MgO–Al2O3 and negative MgO–Sc relationships manifest the cotectic crystallization of plagioclase and olivine, which exist with the presence of plagioclase and olivine phenocrysts and the absence of clinopyroxene phenocrysts. However, the fractionation of clinopyroxene is proven by the positive correlation of MgO and CaO. Thus, MORB samples are believed to show a “clinopyroxene paradox”. The highest magnesium-bearing MORB sample E13-3B (MgO=9.52%) is modelled for isobaric crystallization with COMAGMAT at different pressures. Observed CaO/Al2O3 ratios can be derived from E13-3B only by fractional crystallization at pressure >4 ±1 kbar, which necessitates clinopyroxene crystallization and is not consistent with cotectic crystallization of olivine plus plagioclase in the magma chamber (at pressure ~1 kbar). The initial compositions of the melt inclusions, which could represent potential parental magmas, are reconstructed by correcting for post-entrapment crystallization (PEC). The simulated crystallization of initial melt inclusions also produce observed CaO/Al2O3 ratios only at >4±1 kbar, in which clinopyroxene takes part in crystallization. It is suggested that MORB magmas have experienced clinopyroxene fractionation in the lower crust, in and below the Moho transition zone. The MORB magmas have experienced transition from clinopyroxene+plagioclase+olivine crystallization at >4±1 kbar to mainly olivine+plagioclase crystallization at <1 kbar, which contributes to the explanation of the “clinopyroxene paradox”.  相似文献   

16.
Petrographic, trace element and isotopic evidence demonstrates that magma mixing preceded the eruption of the Garner Mountain andesite. The flow contains reversely zoned plagioclase phenocrysts and amphibole pseudomorphs composed of plagioclase, clinopyroxene, orthopyroxene and opaque oxides. Partially resorbed quartz grains are also present. In contrast to the isotopically uniform matrix, plagioclase phenocrysts have 87Sr/86Sr ratios that correlate negatively with matrix Sr and positively with matrix Rb abundances. These observations demonstrate increasing isotopic disequilibrium between the plagioclase and matrix in the more evolved varieties of the flow.Plagioclase phenocrysts and matrix are assumed to record fractionation-assimilation events in different parts of the magma chamber. Early formed plagioclase phenocrysts crystallized under AFC conditions close to the roof of the chamber and were subsequently entrained in a liquid mixture composed of evolved interstitial liquid held in the partly crystallized roof zone and newly injected parental magma.  相似文献   

17.
The Bonin archipelago represents an uplifted fore-arc terrainwhich exposes the products of Eocene supra-subduction zone magmatism.Chichijima, at the centre of the chain, represents the typelocality for the high-Mg andesitic lava termed boninite. Therange of extrusives which constitute the boninite series volcanicsare present on Chichijima, and are disposed in the sequenceboninite-andesite-dacite with increasing height in the volcano-stratigraphy.Progression to evolved compositions within the Chichijima boniniteseries is controlled by crystal fractionation from a boniniteparental magma containing 15% MgO. Olivine and clinoenstatiteare the initial liquidus phases, but extraction of enstatiticorthopyroxene, followed by clinopyroxene and plagioclase, isresponsible for the general evolution from boninite, throughandesite, to dacite. Some andesites within the overlying MikazukiyamaFormation are petrographically distinct from the main boniniteseries in containing magnetite phenocrysts and a high proportionof plagioclase. As such, these andesites have affinities withthe calc-alkaline series. Major and trace element data for 74 boninitic series rocks fromChichijima are presented. Although major element variation isdominantly controlled by high-level crystal fractionation, thelarge variations in incompatiable trace element concentrationsat high MgO compositions cannot be explained by this mechanism.Nd, Pb, and Sr isotopic data indicate the following: (1) a strongoverprint on 87Sr/86Sr by seawater alteration; (2) Pb isotopeslie above the northern hemisphere reference line (NHRL) andare thus similar to the <30-Ma are and basin lavas of theIzu—Bonin system, and (3) Nd(40 Ma) ranges between 2.8and 6.8 within the boninite series volcanics. Differences inrare-earth elements (REE), Zr, Ti, and 143Nd/144Nd at similardegrees of fractionation can be explained by the addition ofa component of fixed composition from the down-going oceaniccrustal slab to a variably depleted source region within theoverlying wedge. Data presented for Sm/Zr and Ti/Zr indicatethat boninite series volcanics are characterized by low valuesfor both of these ratios. In particular, boninites appear tohave uniquely low Sm/Zr ratios. These characteristics may bethe result of slab melting in the presence of residual amphibole;the resultant melt could combine with typical slab dehydrationfluids and infiltrate the overlying mantle wedge. Such a fluid—meltcomponent could mix either with shallow mantle or directly withprimitive melts from depleted mantle. Trace elements, REE, andisotope data thus point to a model for boninite genesis whichrequires tightly constrained pressure—temperature conditionsin the slab combined with melting of a variably depleted sourcein the overlying wedge. Such constraints are rarely met exceptduring the subduction of juvenile oceanic crust beneath a young,hot overriding plate.  相似文献   

18.
Rare-earth-element, radiogenic and oxygen isotope, and mineral chemical data are presented for tholeiitic and alkaline Quaternary volcanism from Karasu Valley (Hatay, southeastern Turkey). Karasu Valley is the northern segment of the Dead Sea transform fault and is filled with flood-basalt type volcanics of Quaternary age. This valley is an active fault zone that is known as “Karasu fault,” extending in a NE-SW direction. The Karasu Valley basaltic volcanics (KVBV) are subaphyric to porphyritic, with variable amounts of olivine, clinopyroxene, and plagioclase phenocrysts. Alkali basalts are generally characterized by high contents of olivine, clinopyroxene, and plagioclase phenocrysts. Their groundmass contains olivine, clinopyroxene, plagioclase, and Fe-Ti oxides. Tholeiitic basalts are subaphyric to porphyritic (high contents of olivine, clinopyroxene, and plagioclase). Their groundmass is similar to that of alkali basalts. The range of olivine phenocryst and microlite compositions for all analyzed samples is Fo81 to Fo43. Plagioclase compositions in both tholeiitic and alkali basalts range from andesine, An38 to bytownite, An72. Clinopyroxene compositions range from diopside to calcic augite. Most of the olivine, plagioclase, and clinopyroxene phenocrysts are normally zoned and/or unzoned. Fe-Ti oxides in both series are titanomagnetite and ilmenite.

Based on normative and geochemical data, the Karasu Valley basaltic volcanics are mostly olivine and quartz-tholeiites, and relatively lesser amount of alkali olivine-basalts. KVBV have low K2O/Na2O ratios, typically between 0.25 and 0.45. Olivine- and quartz-tholeiites are older than alkali olivine-basalts. Olivine tholeiites have Zr/Nb and Y/Nb ratios similar to alkaline rocks, but their Ba/Nb, Ba/La, and La/Nb ratios are slightly higher than alkali olivine-basalts. In contrast, quartz-tholeiites have the highest Ba/Nb, Ba/La, Zr/Nb, and Y/Nb and the lowest Nb/La ratios among the KVBV. Alkali basalts have 87Sr/86Sr and 143Nd/144Nd ratios ranging from 0.703353 to 0.704410 and 0.512860 to 0.512910, respectively. In contrast, quartz-tholeiites have higher 87Sr/86Sr and lower 143Nd/144Nd ratios, which vary from 0.704410 to 0.705490 and 0.512628 to 0.512640, respectively. Olivine tholeiites have intermediate isotopic compositions ranging from 0.703490 to 0.704780 and 0.512699 to 0.512780, respectively. 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb isotopic ratios of KVBV range from 18.817 to 19.325, 15.640 to 15.718, and 39.054 to 39.223, respectively. The range of O isotope values is between +5.84 and +7.97‰. The higher O and Sr isotopes in olivine- and quartz-tholeiites relative to alkali olivine-basalts can be explained by contamination of magmas by crustal materials.

The KVBV have intraplate chemistry similar to that of other tholeiitic and alkaline basalts in other within-plate environments, and isotopes range from isotopically depleted mantle to enriched isotope compositions similar to some enriched ocean islands. Trace-element and isotope data indicate that the KVBV are derived from a common OIB-like asthenospheric mantle source, but they have experienced different degrees of crustal contamination during their ascent to the surface, contemporaneous with little fractional crystallization. Although quartz-tholeiites display significant effects of crustal contamination, alkali olivine-basalts appear to have negligible or no crustal contamination in their geesis.  相似文献   

19.
Summary The mineral chemistry of several Pliocene alkali basaltic rocks from Burgenland and Styria (Eastern Austria) have been investigated in order to determine the evolution path of the basalt magmas prior to eruption. With their wide range of substitutions, clinopyroxenes provide the best records of the evolution history of rocks. Pyroxene phenocrysts of the investigated basalts show both concentric and sector zoning. The investigation of sector zoned crystals shows, that not only Ti, Al and Fe contents are different in different sectors but there can be significant differences also in their Cr content. This fact apparently suggests that the distribution of Cr between clinopyroxene and melt could be influenced by crystallization kinetics.The depth of crystallization and differentiation of the basalts can be estimated from Ti and Al contents of clinopyroxene phenocrysts. From a combination of data on clinopyroxene composition, compatible trace element contents and mg-values of the rocks, it is concluded, that the alkali basalts of Pauliberg and Steinberg underwent slight olivine and clinopyroxene fractionation in shallow magma chambers prior to eruption, while the nephelinite of Stradnerkogel evolved mainly through clinopyroxene fractionation under high pressure conditions, probably in the upper mantle.
Chemie der Pyroxene und Entwicklung von Alkalibasalten aus dem Burgenland und der Steiermark, Österreich
Zusammenfassung Einige pliozäne alkalibasaltische Gesteine aus dem Burgenland und der Steiermark wurden mineral-chemisch untersucht, um Aufschluß über ihre Evolution vor der Eruption zu erhalten. Klinopyroxene mit ihren vielfältigen Subtitutionsmöglichkeiten erlauben am besten eine Abschätzung der Evolution der Basalte. Pyroxen-Einsprenglinge der Basalte zeigen sowohl konzentrischen als auch sektoralen Zonarbau. Die von uns untersuchten Einsprenglinge zeigen in den verschiedenen Sektoren nicht nur unterschiedliche Gehalte an Ti, Al und Fe, sondern vielfach auch unterschiedliche Cr-Gehalte. Dies macht es wahrscheinlich, daß die Verteilung von Cr zwischen Klinopyroxen und Schmelze von der Kristallisations-Kinetik beeinflußt wird.Die Tiefe in der die Basalte kristallisierten und differenzierten kann von den Ti- und Al-Gehalten der Klinopyroxen- Einsprenglinge abgeschätzt werden. Die Zusammensetzung der Klinopyroxene im Verein mit den Gehalten an kompatiblen Spurenelementen und denmg-Werten der Gesteine erlauben den Schluß, daß die Alkalibasalte von Pauliberg und Steinberg vor ihrer Eruption eine geringfügige Olivinund Klinopyroxen-Fraktionierung in einer seichten Magmakammer erlebten. Der Nephelinit vorn Stradnerkogel hingegen erfuhr hauptsächlich eine Klinopyroxen Fraktionierung unter Hochdruck-Bedingungen, möglicherweise im oberen Erdmantel.

With 8 Figures  相似文献   

20.
Reunion Island consists of an olivine-basalt shield capped by a series of flows and intrusives ranging from hawaiite through trachyte. Eleven rocks representing the total compositional sequence have been analyzed for U, Th and REE.Eight of the rocks (group 1) have positive-slope, parallel, chondrite-normalized REE fractionation patterns. Using a computer model, the major element compositions of group 1 whole rocks and observed phenocrysts were used to predict the crystallization histories of increasingly residual liquids, and allowed semi-quantitative verification of origin by fractional crystallization of the olivine-basalt parent magma. Results were combined with mineral-liquid distribution coefficient data to predict trace element abundances, and existing data on Cr, Ni, Sr and Ba were also successfully incorporated in the model.The remaining three rocks (group 2) have nonuniform positive-slope REE fractionation patterns not parallel to group 1 patterns. Rare earth fractionation in a syenite is explained by partial melting of a source rich in clinopyroxene and/or hornblende. The other two rocks of group 2 are explained as hybrids resulting from mixing of syenite and magmas of group 1.  相似文献   

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