Geochemistry of Kauai volcanics and a mixing model for the origin of Hawaiian alkali basalts

A comprehensive model is developed to explain the major, trace element and strontium and neodymium isotopic characteristics of alkali basalts from Hawaii. The model is similar to that of Chen and Frey (1983) in that it requires mixing of a small melt fraction of MORB-source material with another component to generate the alkalic suite of a particular Hawaiian volcano. It differs from the Chen and Frey model in that the other end-member must be different from primitive mantle if it is to be consistent with both trace element and isotopic data. Alkali basalts and tholeiites from Kauai analyzed in this study show a nearly complete transition in Sr and Nd isotopes. There is a relatively well-constrained array on a Nd-Sr isotope correlation plot that can be explained by two-component mixing of Kauai tholeiite magma and a small amount of melt of East Pacific Rise source rock. After corrections are made for fractional crystallization (involving primarily clinopyroxene and olivine), the Sr and Ba concentrations of Kauai lavas plot along mixing curves defined by the above sources, providing positive tests of the mixing hypothesis. Implications of this model are: (1) the main source of Hawaiian shield-building tholeiites is a mixture of subducted crust, primitive mantle and depleted asthenosphere that has been homogenized prior to melting, (2) early alkalic volcanism (as at Loihi seamount) will be characterized by greater isotopic heterogeneity than will late-stage alkali basalt production, and (3) there are two fundamentally distinct types of alkalic lavas erupted towards the end of magmatism at a given Hawaiian volcano. One represents smaller degrees of melting of the same source that generated shield-building tholeiites (Kohala-type); the other derives from the mixed source discussed in this paper (Haleakala-, Kauai-type).     

Tholeiitic and alkali basalts from the Mid-Atlantic Ridge at 43 ° N

Tholeiitic basalts dredged from the Mid-Atlantic Ridge (MAR) axis at 43 ° N are enriched in incompatible trace elements compared to the ‘ normal’ incompatible element depleted tholeiites found from 49 ° N to 59 ° N and south of 33 ° N on the MAR. The most primitive 43 ° N glasses have MgO/FeO*= 1.2 and coexist with olivine (Fo_90–91) and chrome-rich spinel. The tholeiitic basalts from the MAR 43 ° N are distinct from the strongly incompatible trace element depleted tholeiities found elsewhere in the Atlantic, and have trace element features typical of island tholeiities and MAR axis tholeiites from 45 ° N. Petrographic, major, and compatible trace element trends of the axial valley tholeiites at 43 ° N are consistent with shallow-level fractionation; in particular, evolution from primitive liquids with forsteritic olivine plus chrome spinel as liquidus phases to fractionated liquids with plagioclase plus clinopyroxene as major crystallizing phases. However, each dredge haul has distinctive incompatible trace element abundances. These trace element characteristics require a hetrogeneous mantle or complex processes such as open system fractional crystallization and magma mixing. Alkali basalts (～5% normative nepheline) were dredged from a prominent fracture zone at 43 ° N. Typical of alkali basalts they are strongly enriched (compared to tholeiites) in incompatible elements. Their highly fractionated rare-earth element (REE) abundances require residual garnet during partial melting. The 43 ° N tholeiites and alkali basalts could be derived from a garnet peridotite source with REE contents equal to 2 × chondrites by ～5% and 1% melting, respectively. Alternatively, they could be derived from a moderately light REE enriched source by ～25% and 9.5% melting, respectively.     

Residual glasses and melt inclusions in basalts from DSDP Legs 45 and 46: Evidence for magma mixing

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 (Fo_90–89), 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     

Anhydrous P-T phase relations of near-primary high-alumina basalt from the South Sandwich Islands

Anhydrous P-T phase relations, including phase compositions and modes, are reported from 10–31 kbar for a near-primary high-alumina basalt from the South Sandwich Islands in the Scotia Arc. The water content of natural subduction-related basalt is probably <0.5 wt.% and thus, these results are relevant to the generation of primary basaltic magmas in subduction zones. At high pressures (>27 kbar) garnet is the liquidus phase followed by clinopyroxene, then quartz/coesite at lower temperatures. At intermediate pressures (17–27 kbar), clinopyroxene is the liquidus phase followed by either garnet, quartz, plagioclase, then orthopyroxene or plagioclase, quartz, garnet, then orthopyroxene depending on the pressure within this interval. At all lower pressures, plagioclase is the liquidus phase followed at much lower temperatures (100° C at 5 kbar) by clinopyroxene. The absence of olivine from the liquidus suggests that the composition studied here could not have been derived from a more mafic parent by olivine fractionation at any pressure investigated, and supports the interpretation that it is primary. If so, these results also preclude an origin for this melt by partial melting of olivine-rich mantle periddotite and suggest instead that it was generated by partial melting of the descending slab (quartz eclogite) leaving clinopyroxene, garnet, or both in the residue. The generally flat REE patterns for low-K series subduction related basalts argue against any significant role for garnet, however, and it is thus concluded that the composition studied here was extracted at 20–27 kbar after sufficiently high degrees of partial melting (50%) to totally consume garnet in the eclogite source. Melting experiments on three MORB composition, although not conclusive, are in agreement with this mechanism. Results at 30 kbar support an origin for tonalite/trondhjemite series rocks by lower degrees of melting (15–30%), leaving both garnet and clinopyroxene in the residue.     

Migration and accumulation of ultra-depleted subduction-related melts in the Massif du Sud ophiolite (New Caledonia)

The Massif du Sud is a large ophiolitic complex that crops out in the southern region of New Caledonia (SW Pacific). It is dominated by harzburgite tectonite that locally shows a transitional gradation to massive dunite up section. Clinopyroxene, orthopyroxene and plagioclase progressively appear in dunite up to the transition to layered wehrlite and orthopyroxene–gabbro. The dunite–wehrlite and wehrlite–gabbro contacts are parallel and the latter defines the paleo-Moho.Highly depleted modal, mineral and bulk rock compositions indicate that harzburgites are residues after high degrees (20–30%) of partial melting mainly in the spinel-stability field. Their relative enrichment in HFSE, LREE and MREE is due to re-equilibration of melting residues with percolating melts. Dunite formed in the Moho transition zone by reaction between residual mantle harzburgite and olivine-saturated melts that led to pyroxene dissolution and olivine precipitation. Rare clinopyroxene and plagioclase crystallized in interstitial melt pores of dunite from primitive, low-TiO₂, ultra-depleted liquids with a geochemical signature transitional between those of island arc tholeiites and boninites.Ascending batches of relatively high-SiO₂, ultra-depleted melts migrated through the Moho transition zone and generated wehrlite by olivine dissolution and crystallization of clinopyroxene, orthopyroxene and plagioclase in variable amounts. These liquids were more evolved and were produced by higher degrees of melting or from a more depleted source compared with melts that locally crystallized clinopyroxene in dunite. Ultra-depleted magmas, non-cogenetic with those that formed the Moho transition zone, ascended to the lower crust and generated gabbroic cumulates with subduction-related affinity. Thus, the ultramafic and mafic rocks in the Moho transition zone and lower crust of the Massif du Sud ophiolite are not products of fractional crystallization from a single magma-type but are the result of migration and accumulation of different melts in a multi-stage evolution.The record of high partial melting in the mantle section, and migration and accumulation of ultra-depleted subduction-related melts in the Moho transition zone and lower crust support that the Massif du Sud ophiolite is a portion of forearc lithosphere generated in an extensional regime during the early phases of the subduction zone evolution. Our results show the existence of different types of ultra-depleted melt compositions arriving at the Moho transition zone and lower crust of an infant intraoceanic paleo-arc. Ultra-depleted melts may thus be a significant component of the melt budget generated in oceanic spreading forearcs prior to aggregation and mixing of a large range of melt compositions in the crust.     

Sur la présence de tholéiites à l'île Saint-Paul (Océan Indien)

The basalts and dolerites from Saint-Paul island, located on the east section of the Indian ridge, are reinvestigated. New chemical rock analysis show that they are caracterized by high Fe, low Mg, and various Al contents; they belong to quartz tholeiites and olivine tholeiites of Yoder and Tilley's classification. Two clinopyroxene analysis allow to confirm this tholeiitic relationship. Compared with abyssal tholeiites, those of Saint-Paul are dissimilar in respect to Al₂O₃/CaO and FeO/MgO ratios, Sr and Rb contents (231–308 ppm and 6 to 29 ppm respectively) and 87 Sr/86 Sr values (0,7041–0,7065). Bearing in mind the structural position of the island, this differences are discussed in light of experimental data. Saint-Paul's basalts and dolerites are products a magma fractionated according to a Fernner trend and probably issued from deeper part of the upper mantle than abyssal tholeiites.     

Constraints from melt inclusions and their host olivines on the petrogenesis of Oligocene-Early Miocene Xindian basalts, Chifeng area, North China Craton

The geochemical characteristics of melt inclusions and their host olivines provide important information on the processes that create magmas and the nature of their mantle and crustal source regions. We report chemical compositions of melt inclusions, their host olivines and bulk rocks of Xindian basalts in Chifeng area, North China Craton. Compositions of both bulk rocks and melt inclusions are tholeiitic. Based on petrographic observations and compositional variation of melt inclusions, the crystallizing sequence of Xindian basalts is as follows: olivine (at MgO > ~5.5 wt%), plagioclase (beginning at MgO = ~5.5 wt%), clinopyroxene and ilmenite (at MgO < 5.0 wt%). High Ni contents and Fe/Mn ratios, and low Ca and Mn contents in olivine phenocrysts, combining with low CaO contents of relatively high MgO melt inclusions (MgO > 6 wt%), indicate that Xindian basalts are possibly derived from a pyroxenite source rather than a peridotite source. In the CS-MS-A diagram, all the high MgO melt inclusions (MgO > 6.0 wt%) project in the field between garnet + clinopyroxene + liquid and garnet + clinopyroxene + orthopyroxene + liquid near 3.0 GPa, further suggesting that residual minerals are mainly garnet and clinopyroxene, with possible presence of orthopyroxene, but without olivine. Modeling calculations using MELTS show that the water content of Xindian basalts is 0.3–0.7 wt% at MgO = 8.13 wt%. Using 20–25 % of partial melting estimated by moderately incompatible element ratios, the water content in the source of Xindian basalts is inferred to be ≥450 ppm, much higher than 6–85 ppm in dry lithospheric mantle. The melting depth is inferred to be ~3.0 GPa, much deeper than that of tholeiitic lavas (<2.0 GPa), assuming a peridotite source with a normal mantle potential temperature. Such melting depth is virtually equal to the thickness of lithosphere beneath Chifeng area (~100 km), suggesting that Xindian basalts are derived from the asthenospheric mantle, if the lithospheric lid effect model is assumed.     

华北晚中生代和新生代玄武岩中单斜辉石巨晶来源及其对寄主岩岩浆过程的制约:以莒南和鹤壁为例

本文对华北克拉通晚中生代和新生代碱性玄武质岩石中的单斜辉石巨晶进行了主、微量元素和Sr-Nd同位素的综合研究,发现晚中生代和新生代单斜辉石巨晶存在明显的主、微量元素和同位素组成上的差异。新生代单斜辉石巨晶有Al-普通辉石和次透辉石两类;而中生代单斜辉石巨晶只有Al-普通辉石。新生代单斜辉石SiO_2含量高、REE配分型式为上凸型、LILE和放射性元素含量高,并具有比寄主碱性玄武岩更亏损的Sr和Nd同位素组成;而中生代单斜辉石SiO_2含量低、REE配分型式为LREE富集型、LILE和部分HFSE以及放射性元素含量低,并具有比寄主碱性玄武岩稍富集的Sr和Nd同位素组成;巨晶的结构、矿物成分和地球化学特征,以及Mg-Fe在熔体与单斜辉石间的分配状况皆说明,新生代碱性玄武岩中单斜辉石巨晶是碱性玄武岩浆在高压下结晶的,因此二者是同源的;而中生代单斜辉石巨晶是被寄主岩浆偶然捕获的捕虏晶,是不同源的。华北新生代单斜辉石巨晶存在于碱性玄武岩和拉斑玄武岩中,它们具有比寄主碱性玄武岩更亏损的Sr和Nd同位素组成,说明即使是碱性玄武岩也不能完全代表软流圈来源的原始岩浆,其在上升过程中或多或少存在同位素组成富集的物质的混入。同时,拉斑玄武岩不是碱性玄武质岩浆直接结晶分异的产物,亦不是完全由部分熔融程度的不同造成的。拉斑玄武岩中存在岩石圈地幔物质的贡献或是岩浆房内碱性玄武质岩浆受地壳混染作用的结果。     

Origin of some magmas in oceanic and circum-oceanic regions

Partial melting experiments on spinel-lherzolite, a rock which probably occurs in relatively shallow parts of the oceanic upper mantle, demonstrate that alkali basaltic melt is formed at depths of at least 20 kbar whereas tholeiitic melt is formed at lower pressures (< 15 kbar) under anhydrous conditions. The specimen studied was a relatively iron-rich natural spinel-lherzolite (Fe/Mg+Fe=0.15) and the melts produced have ratios comparable to those obtained in basalts. Slight increase of degree of partial melting produces picritic melt over a wide pressure range. Under hydrous (water-excess) conditions, andesitic melt is produced by partial melting of the same natural spinel-lherzolite and a synthetic lherzolite. The melting experiments on two different abyssal tholeiites from the Mid-Atlantic Ridge suggest that the derivation of olivine tholeiite from a more mafic magma or a mantle peridotite (lherzolite) is possible, but is limited to depths shallower than 25 km under essentially anhydrous conditions, whereas plagioclase tholeiite may have been formed by fractional crystallization at depths of about 20 km in the presence of a small amount (～ 2 wt.%) of water.It is suggested that under mid-ocean ridges, partial melting of spinel-lherzolite at depths shallower than 60 km would produce olivine-tholeiitic magma, which differentiates at shallower levels (20–25 km) under either essentially anhydrous or hydrous (but vapor-absent) conditions to produce abyssal tholeiites of olivine-tholeiite type or plagioclase-tholeiite type. It may be also possible that the former olivine-tholeiite is generated by direct partial melting of plagioclase-lherzolite. Alkali basalts in the oceanic region may be generated at depths greater than 50 km by relatively small degree of partial melting. Along island arcs and continental margins, where the subduction zones probably exist, partial melting of lherzolite would take place in the presence of water that may be supplied by breakdown of hydrous minerals in the subducted oceanic crust, thereby producing andesitic magmas. High-alumina basalt magma could be produced by partial melting of the dehydrated oceanic crust in the subduction zone at depths between 40 and 60 km, where garnet is unstable above the solidus.     

Plume dynamics beneath the African plate inferred from the geochemistry of the Tertiary basalts of southern Ethiopia

Southern Ethiopian flood basalts erupted in two episodes: the pre-rift Amaro and Gamo transitional tholeiites (45-35 million years) followed by the syn-extensional Getra-Kele alkali basalts (19-11 million years). These two volcanic episodes are distinct in both trace element and isotope ratios (Zr/Nb ratios in Amaro/Gamo lavas fall between 7 and 14, and 3-4.7 in the Getra-Kele lavas whereas ²⁰⁶Pb/²⁰⁴Pb ratios fall between 18-19 and 18.9-20, respectively). The distinctive chemistries of the two eruptive phases record the tapping of two distinct source regions: a mantle plume source for the Amaro/Gamo phase and an enriched continental mantle lithosphere source for the Getra-Kele phase. Isotope and trace element variations within the Amaro/Gamo lavas reflect polybaric fractional crystallisation initiated at high pressures accompanied by limited crustal contamination. We show that clinopyroxene removal at high (0.5 GPa) crustal pressures provides an explanation for the common occurrence of transitional tholeiites in Ethiopia relative to other, typically tholeiitic flood basalt provinces. The mantle plume signature inferred from the most primitive Amaro basalts is isotopically distinct from that contributing to melt generation in central Ethiopian and Afar. This, combined with Early Tertiary plate reconstructions and similarities with Kenyan basalts farther south, lends credence to derivation of these melts from the Kenyan plume rather than the Afar mantle plume. The break in magmatism between 35 and 19 Ma is consistent with the northward movement away from the Kenya plume predicted from plate tectonic reconstructions. In this model the Getra-Kele magmatism is a response to heating of carbonatitically metasomatised lithosphere by the Afar mantle plume beneath southern Ethiopia at this time.     

雷琼地区晚新生代玄武岩地球化学：EM2成分来源及大陆岩石圈地幔的贡献

对雷琼地区21个晚新生代玄武岩样品的主量、微量元素和Sr、Nd、Pb同位素分别用湿化学法、ICP-MS和MC-ICPMS进行了测定.这些玄武岩主要为石英拉斑玄武岩,其次为橄榄拉斑玄武岩和碱性玄武岩.大多数样品的微量元素和同位素成分与洋岛玄武岩(OIBs)相似,而且随着SiO_2不饱和度增加,不相容元素含量也增加.除R4-1可能受到地壳混染外,其他样品相对均一的Nd同位素(ε_(Nd)=2.5-6.0)以及变化明显但范围有限的Sr同位素(0.703106～0.704481),可能继承了地幔源区的特征.~(87)Sr/~(86)Sr与~(206)Pb/~(204)Pb的正相关和~(143)Nd/~(144)Nd与~(206)Pb/~(204)Pb的负相关特征暗示DM(软流圈地幔)与EM2(岩石圈地幔)的混合.地幔捕虏体的同位素特征暗示EM2成分不可能存在于尖晶石橄榄岩地幔,而La/Yb和Sm/Yb系统表明岩浆由石榴石橄榄岩部分熔融产生,这意味着EM2成分可能存在于石榴石橄榄岩地幔.雷琼地区玄武岩的地球化学变化可以用软流圈地幔为主的熔体加入不同比例石榴石橄榄岩地幔不同程度熔融产生的熔体来解释:碱性玄武岩和橄榄拉斑玄武岩是软流圈熔体与石榴石橄榄岩地幔较低程度(7%～9%)熔融体混合,而石英拉斑玄武岩是软流圈熔体与石榴石橄榄岩地幔较高程度(10%～20%)熔融体的混合.     

Deep Fractionation of Clinopyroxene in the East Pacific Rise 13°N: Evidence from High MgO MORB and Melt Inclusions

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”.     

The composition and formation of Miocene tholeiites in the Central European Cenozoic plume volcanism (CECV)

Tholeiites accompanying a majority of alkali basalts are restricted to the highly productive central part of the CECV plume activity in Vogelsberg and Hessian Depression. They mainly occur as quartz tholeiites which according to experiments of partial melting and material balances are products of olivine tholeiitic primary melts. The differentiation from olivine to quartz tholeiitic melts took place in lower crustal magma chambers where olivine tholeiitic melt intruded due to a density comparable with that of the country rocks. The fractionation due to separation of olivine and some clinopyroxene caused contamination of tholeiite magmas by tonalitic partial melts from the wall rocks of the magma chambers. The latter process is indicated by relatively high Rb, K and Pb and low Nb concentrations and by Nd, Sr and Pb isotopes. Contaminating crustal melts, which roughly attained a proportion of 10%, contained very low ¹⁴³Nd/¹⁴⁴Nd ratios from a Nd/Sm fractionation as old as 2.6 Ga. This is the first evidence from mafic rocks of this high age in the lower crust beneath Central Europe. Modelling with incompatible elements allows to recognize olivine tholeiites as products of about 1% partial melting of plume rocks consisting of 35% primitive and 65% depleted mantle materials. The production of tholeiites other than alkali basalts is restricted to the highest plume activity and the largest fraction of MORB type source rocks. Received: 10 December 1999 / Accepted: 23 June 2000     

Crystallization processes beneath the southern Mid-Atlantic Ridge (40–55°S), evidence for high-pressure initiation of crystallization

New major and trace element data are reported for a suite of basalts dredge sampled from the southern MAR (40.6-52.5°S) during cruise 9309 of the R/V Maurice Ewing and cruise 32 of the S.A. Agulhas (51-54.5°S). Samples range from aphyric to moderately porphyritic with plagioclase and olivine the dominant phenocryst and microphenocryst phases. Clinopyroxene occurs rarely as a phenocryst phase. Bulk rock and quench glass samples have major element compositions ranging from moderately primitive (Mg#=68.5) to evolved (Mg#=41.1), with a comparable range in incompatible (Zr=54-232 ppm; Nb=0.8-21 ppm) and highly compatible trace element (Ni=51-289 ppm; Cr=39-949 ppm) abundances. Incompatible trace element ratios (e.g., Zr/Nb=5.9-69; Y/Nb=0.88-29; (La/Sm)_N=0.48-2.9) indicate both enriched and depleted MORB occurring along this section of the MAR, agreeing with along-ridge radiogenic isotope ratio variations delineating compositional influences of the off-axis Discovery, and a so-called LOMU-component, and ridge-centered Shona mantle plumes (Douglass et al. 1999; Douglass and Schilling 2000). Major- and trace-element variations, particularly decreasing CaO/Al₂O₃ ratios and relatively constant Sc abundances with decreasing Mg# suggest crystallization of olivine, plagioclase, and clinopyroxene in most of these basalts prior to eruption. Liquid-lines-of-descent, derived from forward modeling of various reasonable parental magma compositions at pressures between 1 atm-8 kbar, confirm clinopyroxene as an early crystallizing phase, along with olivine and plagioclase, and its pivotal role in the compositional evolution of these basalts. Pressures deduced using algorithms of Grove et al. 1992 and Michael and Cornell 1998 indicate crystallization beneath ridge segments unaffected by mantle plumes occurred predominately at depths of 3-6 kbar (10-20 km). Crystallization beneath ridge segments affected by the Discovery and Shona mantle plumes occurred over a larger pressure range (1 atm-~7 kbar), but predominantly at crustal depths (1 atm-3 kbar), possibly due to more constant magma fluxes and higher temperatures in the crust and lithosphere in these regions favoring the existence and longevity of subaxial magma chambers.     

The Cenozoic Basaltic Rocks of Eastern China: Petrology and Chemical Composition

The Cenozoic volcanicity of eastern China is entirely basalticand occurred as relatively small eruptions widely dispersedin space and time, closely associated with graben basins andtheir regional bounding faults. Samples (157) from over 30 sitesin eastern China have been studied. They are predominantly alkalinebasalts, but vary in composition from olivine nephelinites andleucitites to quartz tholeiites. The majority are aphyric butsome contain olivine and clinopyroxene phenocrysts. Whole-rockanalyses (X-ray fluorescence) of all samples for the major and13 trace elements are used, as are the compositions of all themajor mineral phases determined by electron microprobe. It is argued that the most primitive basanites, alkali olivinebasalts, and olivine tholeiites represent primary or near-primarymagmas which were formed by different degrees of partial meltingof the upper mantle at different depths. The olivine tholeiitesrepresent larger degrees of partial melting (8–9%) ofa spinel peridotite at depths of <66 km. The alkalic basaltscarry xenoliths of spinel and garnet peridotite and appear tohave been derived by 1–7% partial melting of a garnetlherzolite (50% ol, 25% opx, 15% cpx, 10% garnet) at depths> 79 km. The olivine nephelinite may have formed by evensmaller degrees of partial melting. Most flows are not primary; the variations in their compositionsare consistent with fractional crystallization from the spectrumof primary parents created by varying degrees of partial meltingof a mineralogically heterogeneous source. The tholeiites havefractionated by the removal of clinopyroxene and some olivine;the alkali basalts by the removal of clinopyroxene with a smallerproportion of olivine. The incompatible behavior of Sr impliesthe absence of plagioclase from any of the fractionating assemblagesand, together with the high Al content of the pyroxene phenocrysts,suggests that much of the fractionation occurred at mantle depthsand pressures. The Cenozoic magmatism of eastern China is seen as a typicalexample of volcanism associated with continental extension.That is, small volumes of predominantly alkalic basalts andolivine tholeiites erupted over a prolonged period and associatedwith extensional basins and their bounding faults. As such,the province is distinct from continental flood basalt provinces.     

Alkaline-ultrabasic mantle-derived magmas, their sources, and crystallization features: Data of melt inclusion studies

To find out the reasons responsible for the diversity of igneous rocks forming the alkaline-ultrabasic carbonatite Krestovskiy massif (the Maimecha–Kotui province, Russia) we have studied melt inclusions in clinopyroxene of trachydolerites, porphyric melanephelinites, and tholeiites. It was established that the homogenization temperatures of inclusions in these rocks are rather close: 1140–1180 °C, 1190–1230 °C, and 1150–1210 °C, respectively. Compositions of melt inclusions in clinopyroxenes from different rocks are significantly different. The chemical composition of clinopyroxene of trachydolerites corresponds to that of trachybasalts and their derivatives. The inclusions are enriched in Sr, Ba, P, and S and their total sum of alkalies (at K ≥ Na) is never less than 5–6 wt.%. Inclusions from the rims of clinopyroxene phenocrysts in porphyric melanephelinites are similar in composition also to inclusions in trachydolerites. But in the cores of clinopyroxene phenocrysts the composition of inclusions corresponds to nephelinite melt. The composition of some melt inclusions in the intermediate and cores zones of clinopyroxene from porphyric melanephelinite has high SiO₂ (53–55 wt.%), MgO (8–9 wt.%) and a low (1–2 wt.%) total sum of alkalies (at Na ≥ K) and is depleted in Al₂O₃ (6–7 wt.%), which is similar to the composition of basaltic komatiites. The composition of inclusions in tholeiites is also basic, highly magnesian, and low-alkaline, Sr and Ba are rare to absent. Compared to the inclusions of basaltic komatiite composition, the inclusions in tholeiites are enriched in Al and depleted in Ca, Ti, and P. The melts trapped in clinopyroxenes from different rocks contain low (0.014–0.018 wt.%) water but they are enriched in F: from 0.37 wt.% in nephelinite melts to 0.1–0.06 wt.% in tholeiite and basaltic komatiite melts. Inclusions in all the rocks under study, host clinopyroxene, and the rocks themselves are significantly enriched in incompatible elements (1–2 orders of magnitude relative to the mantle norm). In tholeiites, the partitioning of these elements is rather uniform, while in trachydolerites and especially in melanephelinites it is contrasting with a drastic depletion in HREE relative to LREE, MREE, and HFSE. A conclusion is made that the Krestovskiy massif was formed by no less than three mantle-derived magmas: melanephelinite, tholeiite and basaltic komatiite. Magmas were generated in different magma sources at different depths with various degrees of enrichment in incompatible elements. These magmas were, most likely, dominated by melanephelinite magma. In intermediate chambers this magma differentiated to form derivative melts of nephelinite, trachydolerite–trachyandesite–trachyte compositions. Komatiite-basalt melts were, most likely, derivatives of primitive meimechite magmas.     

The melting relationships of a madupite from the Leucite Hills,Wyoming, to 30 Kb

The water-undersaturated melting relationships of a mafic, peralkaline, potassic madupite (with about 3% H₂O as shown by chemical analysis) from the Leucite Hills, Wyoming, have been studied at pressures up to 30 kb. At low pressures (<5 kb) leucite is the dominant liquidus phase, but it is replaced at higher pressures by clinopyroxene plus olivine (<5–7 kb), clinopyroxene (7–12.5 kb), clinopyroxene plus minor spinel (12.5–17.5 kb), and clinopyroxene alone (17.5–> 30 kb). At all pressures there is a reaction relationship with falling temperature between melt, olivine and probably clinopyroxene to yield phlogopite. Apatite is stable within the melting interval to pressures above 25 kb. Electron microprobe analyses demonstrate that the clinopyroxene is diopsidic, with low aluminium and titanium contents. Pressure has relatively little effect on the composition of the pyroxene. Phlogopite is also aluminium-poor and has only a moderate titanium content. The experimental results indicate that madupite is not the partial melting product of hydrous lherzolite or garnet lherzolite in the upper mantle and it seems improbable that it is derived by melting of mantle peridotite with a mixed H₂O-CO₂ volatile component. Madupite could, however, be the partial melting product of mica-pyroxenite or mica-olivine-pyroxenite in the upper mantle. It is pointed out that the chemistry of some potassium-rich volcanics may have been affected by volatile transfer and other such processes during eruption and that experimental studies of material affected in this way have little bearing upon the genesis of potassic magmas. Finally, the experimental results enable constraints to be placed upon the P-T conditions of the formation of richterite-bearing mica nodules found in kimberlites and associated rocks. Maximum conditions are 25 kb and 1,100 ° C.     

Porosity of the melting zone and variations in the solid mantle upwelling rate beneath Hawaii: inferences from 238U-230Th-226Ra and 235U-231Pa disequilibria

Measurements of ²³⁸U-²³⁰Th-²²⁶Ra and ²³⁵U-²³¹Pa disequilibria in a suite of tholeiitic-to-basanitic lavas provide estimates of porosity, solid mantle upwelling rate and melt transport times beneath Hawaii. The observation that (²³⁰Th/²³⁸U) > 1 indicates that garnet is required as a residual phase in the magma sources for all of the lavas. Both chromatographic porous flow and dynamic melting of a garnet peridotite source can adequately explain the combined U-Th-Ra and U-Pa data for these Hawaiian basalts. For chromatographic porous flow, the calculated maximum porosity in the melting zone ranges from 0.3–3% for tholeiites and 0.1–1% for alkali basalts and basanites, and solid mantle upwelling rates range from 40 to 100 cm yr⁻¹ for tholeiites and from 1 to 3 cm yr⁻¹ for basanites. For dynamic melting, the escape or threshold porosity is 0.5–2% for tholeiites and 0.1–0.8% for alkali basalts and basanites, and solid mantle upwelling rates range from 10 to 30 cm yr⁻¹ for tholeiites and from 0.1 to 1 cm yr⁻¹ for basanites. Assuming a constant melt productivity, calculated total melt fractions range from 15% for the tholeiitic basalts to 3% for alkali basalts and basanites.     

Comparative Study of Magmatism in East Pacific Rise Versus Nearby Seamounts: Constraints on Magma Supply and Thermal Structure Beneath Mid‐ocean Ridge

Major elements of 2202 basalts from the East Pacific Rise (EPR) and 888 basalts from near-EPR seamounts are used to investigate their differences in magma crystallization pressures and mantle melting conditions. Crystallization pressure calculation from basalts with 5.0wt%相似文献   

Crystal fractionation and partial melting in the petrogenesis of a Proterozoic high-MgO volcanic suite,Ungava, Québec

There is little concensus on the relative importance of crystal fractionation and differential partial melting to the chemical diversity observed within most types of volcanic suites. A resolution to this controversy is best sought in suites containing high MgO lavas such as the Chukotat volcanics of the Proterozoic Cape Smith foldbelt, Ungava, Quebec. The succession of this volcanic suite consists of repetitive sequences, each beginning with olivine-phyric basalt (19-12 wt% MgO), grading upwards to pyroxene-phyric basalt (12-8 wt% MgO) and then, in later sequences, to plagioclase-phyric basalt (7-4 wt% MgO). Only the olivine-phyric basalts have compositions capable of equilibrating with the upper mantle and are believed to represent parental magmas for the suite. The pyroxene-phyric and plagioclase-phyric basalts represent magmas derived from these parents by the crystal fractionation of olivine, with minor chromite, clinopyroxene and plagioclase. The order of extrusion in each volcanic sequence is interpreted to reflect a density effect in which successively lighter, more evolved magmas are erupted as hydrostatic pressure wanes. The pyroxene-phyric basalts appear to have evolved at high levels in the active part of the conduit system as the eruption of their parents was in progress. The plagioclase-phyric basalts may represent residual liquids expelled from isolated reservoirs along the crust-mantle interface during the late stages of volcanic activity.A positive correlation between FeO and MgO in the early, most basic olivine-phyric basalts is interpreted to reflect progressive adiabatic partial melting in the upper mantle. Although this complicates the chemistry, it is not a significant factor in the compositional diversification of the volcanic suite. The preservation of such compositional melting effects, however, suggests that the most basic olivine-phyric basalts represent primitive magmas. The trace element characteristics of these magmas, and their derivatives, indicate that the mantle source for the Chukotat volcanics had experienced a previous melting event.