Geochemical and mineralogical evidence for the occurrence of at least three distinct magma types in the ‘famous’ region

Bulk rock major and trace element variations in selected basalts from the Famous area, in conjunction with a detailed study of the chemical compositions of phenocryst minerals and associated melt inclusions are used to place constraints on the genetic relationship among the various lava types. The distribution of NiO in olivine and Cr-spinel phenocrysts distinguishes the picritic basalts, plagioclase phyric basalts and plagioclase-pyroxene basalts from the olivine basalts. For a given Mg/Mg+Fe²⁺ atomic ratio of the mineral, the NiO content of these phenocrysts in the former three basalt types is low relative to that in the phenocrysts in the olivine basalts. The Zr/Nb ratio of the lavas similarly distinguishes the olivine basalts from the plagioclase phyric and plagioclase pyroxene basalts and, in addition, distinguishes the picritic basalts from the other basalt types. These differences indicate that the different magma groups could not have been processed through the same magma chamber, and preclude any direct inter-relationship via open or closed system fractional crystallization.The Fe-Mg partitioning between olivine and host rock suggests that the picritic basalts represent olivine (±Cr-spinel) enriched magmas, derived from a less MgO rich parental magma. The partitioning of Fe and Mg between olivine, Cr-spinel and coexisting liquid is used to predict a primary magma composition parental to the picritic basalts. This magma is characterized by relatively high MgO (12.3%) and CaO (12.6%) and low FeO^* (7.96%) and TiO₂ (0.63%).Least squares calculations indicate that the plagioclase phyric basalts are related to the plagioclase-pyroxene basalts by plagioclase and minor clinopyroxene and olivine accumulation. The compositional variations within the olivine basalts can be accounted for by fractionation of plagioclase, clinopyroxene and olivine in an open system, steady state, magma chamber in the average proportions 453223. It is suggested that the most primitive olivine basalts can be derived from a pristine mantle composition by approximately 17% equilibrium partial melting. Although distinguished by its higher Zr/Nb ratio and lower NiO content of phenocryst phases, the magma parental to the picritic basalts can be derived from a similar source composition by approximately 27% equilibrium partial melting. It is suggested that the parental magma to the plagioclase-pyroxene and plagioclase phyric basalts might have been derived from greater depth resulting in the fractionation of the Zr/Nb ratio by equilibration with residual garnet.C.O.B. Contribution No. 722     

Petrology,volume and age relations of alkaline and saturated peralkaline volcanics from Terceira,Azores

Four volcanoes form Terceira, one of the islands of the Azores group; three contain both basaltic and peralkaline and one only peralkaline rocks. A recently active basaltic fissure zone trends NW-SE across the island.The rocks fall into the alkaline olivine basalt suite although some young basalts are of transitional affinity. The geochemistry shows two general basaltic series: 1) undersaturated, found in lavas of the oldest volcano and in some recent fissure zone basalts and hawaiites; 2) saturated, found in the younger basaltic lavas.Since the emergence of Terceira there has been a contemporaneity of basalt and salic peralkaline lavas. The younger rocks show a bimodal composition distribution, the most voluminous compositions being alkali olivine basalt and comendite with negligible volume in the benmoreite-trachyte range. Two processes appear viable for the derivation of voluminous oversaturated peralkaline rocks: 1) partial melting of upper mantle material giving small magma batches of contrasting composition or 2) fractionation from a transitional basaltic parental magma.Now at Department of Geology, Victoria University of Wellington, New Zealand.     

汉诺坝玄武岩化学及其演化趋势

汉诺坝玄武岩于中新世喷出。除了碱性玄武岩以外,夏威夷岩广泛分布,还有苦橄玄武岩和马盖尔岩。有三个岩浆演化趋势:地壳岩浆房内橄榄石和单斜辉石斑晶组合的分离作用产生了从夏威夷岩到马盖尔岩的肯尼迪分异趋势;莫霍面附近的岩浆房内石榴石、普通辉石、歪长石和钛铁矿巨晶组合的分离作用导致了由原生夏威夷岩和碱性玄武岩经过进化的夏威夷岩和碱性玄武岩到拉斑玄武岩的跨式B型分异趋势;原生岩浆演化趋势。     

The genesis of basaltic magmas

This paper reports the results of a detailed experimental investigation of fractionation of natural basaltic compositions under conditions of high pressure and high temperature. A single stage, piston-cylinder apparatus has been used in the pressure range up to 27 kb and at temperatures up to 1500° C to study the melting behaviour of several basaltic compositions. The compositions chosen are olivine-rich (20% or more normative olivine) and include olivine tholeiite (12% normative hypersthene), olivine basalt (1% normative hypersthene) alkali olivine basalt (2% normative nepheline) and picrite (3% normative hypersthene). The liquidus phases of the olivine tholeiite and olivine basalt are olivine at 1 Atmosphere, 4.5 kb and 9 kb, orthopyroxene at 13.5 and 18 kb, clinopyroxene at 22.5 kb and garnet at 27 kb. In the alkali olivine basalt composition, the liquidus phases are olivine at 1 Atmosphere and 9 kb, orthopyroxene with clinopyroxene at 13.5 kb, clinopyroxene at 18 kb and garnet at 27 kb. The sequence of appearance of phases below the liquidus has also been studied in detail. The electron probe micro-analyser has been used to make partial quantitative analyses of olivines, orthopyroxenes, clinopyroxenes and garnets which have crystallized at high pressure.These experimental and analytical results are used to determine the directions of fractionation of basaltic magmas during crystallization over a wide range of pressures. At pressures corresponding to depths of 35–70 km separation of aluminous enstatite from olivine tholeiite magma produces a direct fractionation trend from olivine tholeiites through olivine basalts to alkali olivine basalts. Co-precipitation of sub-calcic, aluminous clinopyroxene with the orthopyroxene in the more undersaturated compositions of this sequence produces derivative liquids of basanite type. Magmas of alkali olivine basalt and basanite type represent the lower temperature liquids derived by approximately 30% crystallization of olivine-rich tholeiite at 35–70 km depth. At depths of about 30 km, fractionation of olivine-rich tholeiite with separation of both olivine and low-alumina enstatite, joined at lower temperatures by sub-calcic clinopyroxene, leads to derivative liquids with relatively constant SiO₂ (48 to 50%) increasingly high Al₂O₃ (15–17%) contents and retaining olivine + hypersthene normative chemistry (5–15% normative olivine). These have the composition of typical high-alumina olivine tholeiites. The effects of low pressure fractionation may be superimposed on magma compositions derived from various depths within the mantle. These lead to divergence of the alkali olivine basalt and tholeiitic series but convergence of both the low-alumina and high-alumina tholeiites towards quartz tholeiite derivative liquids.The general problem of derivation of basaltic magmas from a mantle of peridotitic composition is discussed in some detail. Magmas are considered to be a consequence of partial melting but the composition of a magma is determined not by the depth of partial melting but by the depth at which magma segregation from residual crystals occurs. Magma generation from parental peridotite (pyrolite) at depths up to 100 km involves liquid-crystal equilibria between basaltic liquids and olivine + aluminous pyroxenes and does not involve garnet. At 35–70 km depth, basaltic liquids segregating from a pyrolite mantle will be of alkali olivine basalt type with about 20% partial melting but with increasing degrees of partial melting, liquids will change to olivine-rich tholeiite type with about 30% melting. If the depth of magma segregation is about 30 km, then magmas produced by 20–25% partial melting will be of high-alumina olivine tholeiite type, similar to the oceanic tholeiites occurring on the sea floor along the mid-oceanic ridges.Hypotheses of magma fractionation and generation by partial melting are considered in relation to the abundances and ratios of trace elements and in relation to isotopic abundance data on natural basalts. It is shown that there is a group of elements (including K, Ti, P, U, Th, Ba, Rb, Sr, Cs, Zr, Hf and the rare-earth elements) which show enrichment factors in alkali olivine basalts and in some tholeiites, which are inconsistent with simple crystal fractionation relationships between the magma types. This group of elements has been called incompatible elements referring to their inability to substitute to any appreciable extent in the major minerals of the upper mantle (olivine, aluminous pyroxenes). Because of the lack of temperature contrast between magma and wall-rock for a body of magma near to its depth of segregation in the mantle, cooling of the magma involves complementary processes of reaction with the wall-rook, including selective melting and extraction of the lowest melting fraction. The incompatible elements are probably highly concentrated in the lowest melting fraction of the pyrolite. The production of large overall enrichments in incompatible elements in a magma by reaction with and highly selective sampling of large volumes of mantle wall-rock during slow ascent of a magma is considered to be a normal, complementary process to crystal fractionation in the mantle. This process has been called wall-rock reaction. Magma generation in the mantle is rarely a simple, closed-system partial melting process and the isotopic abundances and incompatible element abundances of a basalt as observed at the earth's surface may be largely determined by the degree of reaction with the mantle or lower crustal wall-rocks and bear little relation to the abundances and ratios of the original parental mantle material (pyrolite).Occurrences of cognate xenoliths and xenocrysts in basalts are considered in relation to the experimental data on liquid-crystal equilibria at high pressure. It is inferred that the lherzolite nodules largely represent residual material after extraction of alkali olivine basalt from mantle pyrolite or pyrolite which has been selectively depleted in incompatible elements by wall-rock reaction processes. Lherzolite nodules included in tholeiitic magmas would melt to a relatively large extent and disintegrate, but would have a largely refractory character if included in alkali olivine basalt magma. Other examples of xenocrystal material in basalts are shown to be probable liquidus crystals or accumulates at high pressure from basaltic magma and provide a useful link between the experimental study and natural processes.     

Trace element geochemistry of high alumina basalt - Andesite - Dacite - Rhyodacite lavas of the Main Volcanic Series of Santorini Volcano,Greece

Trace element systematics throughout the cal-calkaline high alumina basalt — basaltic andesite — andesite — dacite — rhyodacite lavas and dyke rocks of the Main Volcanic Series of Santorini volcano, Greece are consistent with the crystal fractionation of observed phenocryst phases from a parental basaltic magma as the dominant mechanism involved in generating the range of magmatic compositions. Marked inflection points in several variation trends correspond to changes in phenocryst mineralogy and divide the Main Series into two distinct crystallisation intervals — an early basalt to andesite stage characterised by calcic plagioclase+augite+olivine separation and a later andesite to rhyodacite stage generated by plagioclase augite+hypersthene+magnetite+apatite crystallisation. Percent solidification values derived from ratios of highly incompatible trace elements agree with previous values derived from major element data using addition-subtraction diagrams and indicate that basaltic andesites represent 47–69%; andesites 70–76%; dacites ca. 80% and rhyodacite ca. 84% crystallisation of the initial basalt magma. Least squares major element mixing calculations also confirm that crystal fractionation of the least fractionated basalts could generate derivative Main Series lavas, though the details of the least squares solutions differ significantly from those derived from highly incompatible element and addition-subtraction techniques. Main Series basalts may result from partial melting of the mantle asthenosphere wedge followed by limited olivine+pyroxene+Cr-spinel crystallisation on ascent through the sub-Aegean mantle and may fractionate to more evolved compositions at pressures close to the base of the Aegean crust. Residual andesitic to rhyodacite magmas may stagnate within the upper regions of the sialic Aegean crust and form relatively high level magma chambers beneath the southern volcanic centres of Santorini. The eruption of large volumes of basic lavas and silicic pyroclastics from Santorini may have a volcanological rather than petrological explanation.     

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     

The Petrology of the Lavas of Grande Comore

The four volcanic islands comprising the Comores archipelagoform a linear rise across the northern end of the MozambiqueChannel. Volcanism migrated westward from the now deeply dissectedand partially submerged Mayotte to the active Kartala volcanoon Grande Comore. The volcanic rocks on all the islands consistof silica–undersaturated basalts and their derivatives. Grande Comore is formed of two coaleseing shield volcanoes,La Grille in the north and Kartala in the south. The lavas ofKartala are entirely alkali basalts, with abundant ankaramiticand oceanitic varieties, containing an average of 3.7 wt percent normative nepheline. They represent a series resultingfrom low–pressure (< 8kb) fractional crystallizationof alkali basalt parent magma. The formation of this parentmagma can be explained as resulting from more than 10 per centpartial melting of garnet lherzolite upper mantle at pressuresaround 30 kb, with some high–pressure (> 25 kb) fractionationof harzburgite, garnet harzburgite, and either garnet wehrliteor ecogite, followed by polybaric fractionation of olivine±clinopyroxene during ascent. They La Grille lavas are basanitie, with an average of 11–5wt per cent normative nepheline and some normative leucite,and contain only olivine as an important phenocryst phase. Theyare explicable as originating from less than 10 per cent partialmelting of garnet I herzolite upper mantle, with substantialhigh–pressure (> 25 kb) fractionation of garnet wehrliteor eclogite. Interuption of this high–pressure(> 25kb) fractionation at different stages resulted in one trendof chemical variation, on which was superimposed a second trendby polybaric fractionation of lherzolite, wehrlite, and dunite,now found as inclusions in the lavas.     

鲁西青山组火山岩形成的构造背景及其成因探讨:主元素和微量元素证据

研究区内火山岩从基性—中性—中酸性都有出露，包括橄榄玄武岩、安山岩和英安岩，且都属于非碱性系列。通过对主元素和微量元素的研究，认为本区火山岩为滞后型弧(陆缘弧)火山作用的产物。源区由于存在大量的因俯冲作用进入地幔的陆壳物质以及流体的交代作用，从而出现富含金云母和不相容元素的交代富集型地幔源，并具有壳源的元素组成特征。火山岩的形成是富集地幔部分熔融的结果，但在成岩过程中可能存在单斜辉石、斜长石、橄榄石和Ti—Fe氧化物等矿物的分离结晶作用，以及橄榄石的堆晶作用。     

扬子地块北缘新元古代望江山层状岩体矿物成分和铂族元素特征:对岩浆演化过程和构造环境的制约

望江山层状岩体位于扬子地块北缘新元古代汉南杂岩带中,岩体从底部到顶部由超镁铁质岩过渡为中性岩:底部主要由辉石岩和橄长岩组成;中部为辉长苏长岩和辉长岩;上部为辉长岩和闪长岩。研究以中部岩相带橄榄辉长苏长岩、辉长苏长岩和辉长岩为对象,通过主要矿物的主微量元素和全岩主微量元素的分析,查明望江山岩体来源于尖晶石二辉橄榄岩组成的大陆下岩石圈地幔,并且地幔源区受到了来自俯冲板片流体的交代,岩体中部带的母岩浆为拉斑玄武质岩浆。钛铁矿—磁铁矿矿物对成分计算表明,母岩浆在形成时具有较高氧逸度。通过单斜辉石压力计得到岩体的侵位深度约为12.9~18 km。对岩体母岩浆橄榄石分离结晶过程的模拟计算表明,中部带橄榄石为母岩浆经过~28%分离结晶的产物。此外,铂族元素（PGE）组成暗示岩体并未经历过大规模的硫化物熔离,可能与缺乏地壳物质混染有关。岩体中单斜辉石与岛弧环境堆晶岩中单斜辉石成分相似,不同于裂谷环境中堆晶单斜辉石的成分;同时,全岩Th/Yb和Nb/Yb比值也与岛弧玄武岩比值相似,因此矿物和全岩成分均说明望江山层状岩体应形成于岛弧环境。研究认为扬子北缘在新元古代长期的俯冲过程中,大洋板片断离导致软流圈上涌,提供热源使交代大陆下岩石圈地幔部分熔融形成具有岛弧特征的镁铁质岩浆,在局部伸展环境中上升侵位形成汉南杂岩带中镁铁—超镁铁质层状岩体。      

大兴安岭哈拉哈河-绰尔河第四纪火山岩地幔源区与岩浆成因

哈拉哈河-绰尔河第四纪火山地处重力梯度带上的大兴安岭中段。火山岩主要类型为钠质系列碱性橄榄玄武岩。火山岩大离子亲石元素和轻稀土元素相对富集,轻重稀土分异程度弱((La/Yb)N=8～12),稀土元素和微量元素配分曲线与大同碱性玄武岩平行,总体上表现出与OIB相似的特征。在Sr-Nd-Pb同位素组成特征上表现出亏损地幔的特点(εNd=4.8～5.9),接近MORB的源区范围。哈拉哈河-绰尔河第四纪火山岩岩浆由轻稀土富集的石榴子石二辉橄榄岩低程度(8%～15%)部分熔融产生,火山岩高MgO(>9%)、Ni(>200×10-6)和Mg#(60～70),表明它们是较原始的岩浆,岩浆上升过程经历了橄榄石和辉石为主的弱分离结晶作用,没有受到地壳物质明显混染。区域伸展作用引发软流圈地幔上涌是哈拉哈河-绰尔河第四纪火山的岩浆成因。     

Geochemistry and tectonic setting of mafic rocks from the Othris Ophiolite,Greece

We present new geochemical analyses of minerals and whole rocks for a suite of mafic rocks from the crustal section of the Othris Ophiolite in central Greece. The mafic rocks form three chemically distinct groups. Group 1 is characterized by N-MORB-type basalt and basaltic andesite with Na- and Ti-rich clinopyroxenes. These rocks show mild LREE depletion and no HFSE anomalies, consistent with moderate degrees (~15%) of anhydrous partial melting of depleted mantle followed by 30–50% crystal fractionation. Group 2 is represented by E-MORB-type basalt with clinopyroxenes with higher Ti contents than Group 1 basalts. Group 2 basalts also have higher concentrations of incompatible trace elements with slightly lower HREE contents than Group 1 basalts. These chemical features can be explained by ~10% partial melting of an enriched mantle source. Group 3 includes high MgO cumulates with Na- and Ti-poor clinopyroxene, forsteritic olivine, and Cr-rich spinel. The cumulates show strong depletion of HFSE, low HREE contents, and LREE enrichments. These rocks may have formed by olivine accumulation from boninitic magmas. The petrogenesis of the N-MORB-type basalts and basaltic andesites is in excellent agreement with the melting conditions inferred from the MOR-type peridotites in Othris. The occurrence of both N- and E-MORB-type lavas suggests that the mantle generating the lavas of the Othris Ophiolite must have been heterogeneous on a comparatively fine scale. Furthermore, the inferred parental magmas of the SSZ-type cumulates are broadly complementary to the SSZ-type peridotites found in Othris. These results suggest that the crustal section may be genetically related to the mantle section. In the Othris Ophiolite mafic rocks recording magmatic processes characteristic both of mid-ocean ridges and subduction zones occur within close spatial association. These observations are consistent with the formation of the Othris Ophiolite in the upper plate of a newly created intra-oceanic subduction zone. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Evidence for the role of phlogopite in the genesis of alkali basalts

Evaluation of available experimental and petrochemical evidence suggests that variations of potassium, titanium and aluminium in basalts can be explained by the melting of titaniferous phlogopite at depths exceeding about 60 km in the upper mantle. For tholeiitic basalts, an inverse covariance is recognised between titanium and aluminium which is probably controlled by the depth of magma segregation. The relative effects of pressure and phlogopite breakdown have been estimated for selected suites of alkali basalt.     

The geochemistry and petrogenesis of dolerites and gabbros from the Tertiary central volcanic complex of Slieve Gullion,North East Ireland

Basaltic magmas emplaced into the root zone of the Slieve Gullion volcano have crystallised to rocks varying in texture from dolerite to gabbro. A mineralogical variation from olivine bearing to quartz bearing varieties has been recorded and with the presence of coexisting Ca-rich and Ca-poor pyroxenes, a tholeiitic assemblage is indicated.Geochemical data confirm this prognosis and a continuous spread of compositions from basalt to tholeiitic andesite are interpreted in terms of fractional crystallisation. Modelling of the fractional crystallisation processes indicate an approach to cotectic conditions with fractionation at low pressures involving olivine, plagioclase, clinopyroxene and Ti-magnetite. Primitive magma compositions, indicated by low values of D.I. and 100 Mg/Mg + Fe²⁺ (atomic)>61, show low concentrations of the large ion lithophile elements such as Rb, Ba, Zr, Y, and K. The relatively high CaO content (>11 %) of these rocks invite comparison with high-calcium low-alkali tholeiitic liquids recognised in extrusive and intrusive magmas elsewhere in the North Atlantic Tertiary volcanic province and with magmas currently erupted at active spreading ridges.In north west Britain the field and stratigraphic distribution of these high-calcium low-alkali magmas suggests that they occupy a distinct chronological niche towards the top of the Palaeocene-Eocene volcanic succession succeeding eruption of mildly alkali and transitional basalts. As such, the refractory (high CaO, MgO, etc.) and large ion lithophile depleted geochemistry can be explained either by differential partial melting in the upper mantle source region or melting of a depleted and refractory mantle source which has already contributed to basalt genesis.     

Nickel content of basaltic magmas: identification of primary magmas and a measure of the degree of olivine fractionation

Available NiO analyses of olivine in peridotites of probable mantle origin are consistent in giving values around 0.40 weight per cent. Assuming that basaltic magma forming from the mantle was in equilibrium with such peridotitic olivine, the NiO content of primary basaltic magmas is estimated to be about 0.030–0.050 weight per cent. The fractionation behaviour of nickel in basaltic magma due to the crystallization of olivine has been calculated using constant NiMg and FeMg exchange partition coefficients between olivine and magma. It is shown that the NiO content of both magma and olivine decreases by 50 per cent after fractional crystallization of 6–12 per cent of olivine. The nickel distribution in some basaltic rocks and olivines is examined in the light of these results, and it is suggested that basaltic magmas, such as some of the ocean-floor basalt and the Hawaiian tholeiite and alkali basalts, represent primary magmas from mantle peridotites.     

Geochemistry,petrogenesis and tectonic significance of the basic volcanic units of the Zildat ophiolitic mélange,Indus suture zone,eastern Ladakh (India)

Abstract

Basic volcanic rocks within the Zildat ophiolitic mélange of Indus suture zone in eastern Ladakh are medium to fine grained with partially preserved primary texture and mineralogy. These rocks are predominantly alkaline basalt with high Nb/Y and enriched incompatible trace element characteristics, similar to those of the oceanic island basalt (OIB). The minor sub-alkaline basaltic rocks resemble N-type mid ocean ridge basalt (N-MORB) but with much lower abundances of incompatible trace element including REE. The alkaline rocks probably generated through variable, but low degrees of partial melting of enriched mantle source and evolved through high pressure olivine and clinopyroxene fractionation. Low pressure plagioclase and Fe- Ti oxide do not appear to be major fractionating phases. Limited data on the sub-alkaline rocks suggest that their parental melts were derived from mantle sources some what similar to that of N- MORB. Significant role of added cumulates of olivine, clinopyroxene and Fe- Ti oxides is also indicated in their genesis. Ophiolitic mélanges all along the Indus suture zone appear to have formed due to the accumulation of mélange material in the upper part of the subduction zone where they suffered glaucophanitic (blueschist) metamorphism and retrograded partially to greenschist grade as these were subsequently obducted to its present position probably during the Cenozoic Himalayan orogeny due to collision of Indian and Eurasian plates.     

Picrite basalts and related lavas from the Deccan Traps of Western India

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.     

西南暗色岩铜镍硫化物矿化岩体与峨眉山玄武岩的关系--以云南金宝山岩体为例

内容提要本文以金宝山为典型实例,根据元素地球化学特征探讨了西南暗色岩铜镍硫化物矿化岩体与峨眉山玄武岩的关系。分析表明,金宝山超镁铁岩与低钛峨眉山玄武岩在元素地球化学特征上具有一致的岩浆成因属性,两者在成岩机制上互补,低钛峨眉山玄武岩普遍经历了橄榄石结晶分异和硫化物熔离亏损作用,金宝山成矿岩体则与低钛峨眉山玄武岩同源岩浆深部分异的堆晶相相对应,由堆晶橄榄石及熔离硫化物和部分残余熔体构成的“晶-糊”侵位形成,因此认为铜镍硫化物矿床成矿岩体与低钛峨眉山玄武岩为同源异相产物。     

广东三水盆地火山岩: 地球化学特征及成因--兼论火山岩性质的时空演化和南海形成的深部过程

位于中国东南部的三水盆地、珠江口盆地、雷琼半岛和北部湾地区广泛分布新生代火山岩。火山岩的形成时间具有从内陆向沿海变新的特点,早第三纪三水和珠江口盆地火山岩具有由玄武岩与粗面岩-流纹岩构成的双峰式特点。其中玄武岩和粗面岩的微量元素和稀土元素的配分形式相似,富集大离子亲石元素并且有相似的εNd(T)同位素组成(2.34～6.4),说明它们来自相同的地幔源区,为同源岩浆演化的产物。玄武岩和粗面岩经历了不同的结晶分异过程,其中玄武岩在较深部岩浆房中经历橄榄石和单斜辉石为主的分离结晶作用,而粗面岩则是在浅部岩浆房中由玄武岩浆分异形成的过渡性岩浆再经过强烈的钾长石和斜长石、以及磷灰石的结晶分异形成的。晚第三纪珠江口盆地和北部湾火山岩、雷琼半岛第四纪火山岩则由碱性和拉斑玄武岩构成。这些火山岩的形成时间和地球化学和同位素特征表明它们经历了连续的软流圈地幔上涌和部分熔融过程,受控于自晚中生代以来的地幔柱构造。南海的形成是地幔柱活动引起的地幔上涌和大陆裂解作用的结果。     

Geochemistry and petrogenesis of a basalt-benmoreite-trachyte suite from the southern part of the Gregory Rift,Kenya

In the southern Gregory Rift valley a series of transitional basalt, ferrobasalt, and benmoreite flows (1.65–1.4 Myr) is overlain by flood trachyte lavas (1.3–0.9 Myr). Mass balance calculations for major element compositions of rocks of this suite and their phenocrysts and microphenocrysts suggest that the ferrobasalts and benmoreites formed from magma resembling the most primitive basalt by closed system fractionation of plagioclase, clinopyroxene, olivine, titanomagnetite, and apatite. The trachytes formed from evolved magmas largely by alkali feldspar fractionation. Estimates of phenocryst and liquid densities and Rayleigh-law modelling of trace element contents support these conclusions. From Rayleigh-law modelling, we derived a set of effective distribution coefficients. Partial melting of crustal rocks or volatile transfer processes had no significant effect on the petrogenesis of this suite. The duration of the eruptive cycle, cooling time calculations, and mass balance calculations suggest that fractionation occurred in a magma reservoir with volume of at least 3 × 10⁴ km³ during an interval of about 0.8 Myr. Temperatures during fractionation probably ranged from about 1200 °C to 900 °C, and pressures may have been roughly 5 to 8 Kb. We suggest that rift development was accompanied by large-scale injection of basaltic magma and dilation of the crust, extensive fractionation, preferential eruption of low-density and fluid trachytic flood lavas, and by several episodes of normal faulting.     

河北汉诺坝碱性玄武岩的源区和成因

我国华北北部新近纪喷发的汉诺坝玄武岩,岩层出露比较完整,普遍含有超镁铁岩包体和各种高压巨晶。大麻坪代黄沟剖面出露较好,主要岩性为玄武岩,从上到下可分为上三、二、一层和底层。岩相学观察显示这些玄武岩含有1%~5%的捕虏晶且斑晶数量很少。橄榄岩包体为尖晶石二辉橄榄岩,轻稀土略微亏损,轻重稀土无分馏,显示这是只经过少量部分熔融后的原始地幔包体。通过对代黄沟碱性玄武岩中橄榄石、辉石和斜长石等斑晶或捕虏晶的矿物学分析,得出它们的成分变化是玄武岩混合了分解的地幔橄榄岩快速上升造成的。玄武岩的主量元素与二辉橄榄岩相平衡的原生熔体相比,Mg#(52.0~62.7)以及CaO(7.3%~8.5%)、Ni((82~192)×10-6)和Cr((65~192)×10-6)含量都较低。玄武岩的稀土分配模式为轻稀土富集的右倾型,δEu=1.01~1.05,δCe=0.95~1.02,富集高场强元素Nb、Ta、Zr及大离子亲石元素Ba、Sr。玄武岩痕量元素Ba/Rb和Rb/Sr的比值显示源区可能遭受过流体的交代作用。同时,痕量元素显示这一系列玄武岩主要受到部分熔融的控制,大量的结晶分异并未发生,且源区残留石榴子石。分析认为玄武岩岩浆应该是原生岩浆,而不是演化岩浆,影响整个岩浆的形成的过程可能是部分熔融而不是分离结晶。基于目前已发表的实验岩石学结果和理论分析认为汉诺坝玄武岩与辉石岩类相平衡,源区主要矿物相为单斜辉石和石榴子石,可能存在少量的橄榄石。