Plagioclase buoyancy in oceanic basalts: Chemical effects

Certain petrological features of oceanic volcanic and plutonic rocks are not completely consistent with previously proposed models of crystal fractionation or magma mixing. For example, Sr is often higher in the differentiated basalts of a suite of aphyric rocks than in the relatively primitive basalts even though the differentiated basalts have apparently been produced by crystallization of large amounts of plagioclase with olivine and clinopyroxene. Additionally, oceanic basalts and gabbroic rocks often contain plagioclase crystals in excess of the appropriate cotectic proportions. Certain differentiated oceanic basaltic glasses and aphyric rocks crystallize plagioclase as the liquidus mineral, which would seem inconsistent with the strongly cotectic nature of the olivine + plagioclase + liquid surface.It is proposed here that plagioclase in mid-ocean ridge magma chambers separates from the basaltic liquid that it crystallizes in at a slower rate than does co-crystallizing olivine or pyroxene. Magma mixing in which a portion of the plagioclase remains suspended in the liquid during crystallization results in much more complex liquid lines of descent in mixed magmas and appears to resolve the apparent discrepancies noted above.     

Crystallization Orders and Phase Chemistry of Glassy Lavas from the Pillow Sequences, Troodos Ophiolite, Cyprus

Three genetically unrelated magma suites are found in the extrusivesequences of the Troodos ophiolite, Cyprus. A stratigraphicallylower pillow lava suite contains andesite and dacite glassesand shows the crystallization order plagioclase; augite, orthopyroxene;titanomagnetite (with the pyroxenes appearing almost simultaneously).These lavas can in part be correlated chemically and mineralogicallywith the sheeted dikes and the upper part of the gabbro complexof the ophiolite. The second magma suite is represented in astratigraphically upper extrusive suite and contains basalticandesite and andesite glasses with the crystallizaton orderchromite; olivine; Ca-rich pyroxene; plagioclase. This magmasuite can be correlated chemically and mineralogically withparts of the ophiolitic ultramafic and mafic cumulate sequence,which has the crystallization order olivine; Ca-rich pyroxene;orthopyroxene; plagioclase. The third magma suite is representedby basaltic andesite lavas along the Arakapas fault zone andshows a boninitic crystallization order olivine; orthopyroxene;Ca-rich pyroxene; plagioclase. One-atmosphere, anhydrous phaseequilibria experiments on a lava from the second suite indicateplagioclase crystallization from 1225?C, pigeonite from 1200?C,and augite from 1165?C. These experimental data contrast withthe crystallization order suggested by the lavas and the associatedcumulates. The observed crystallization orders and the presenceof magmatic water in the fresh glasses of all suites are consistentwith evolution under relatively high partial water pressures.In particular, high P_H2O (1–3 kb) can explain the lateappearances of plagioclase and Ca-poor pyroxene in the majorityof the basaltic andesite lavas as the effects of suppressedcrystallization temperatures and shifting of cotectic relations.The detailed crystallization orders are probably controlledby relatively minor differences in the normative compositionsof the parental magmas. The basaltic andesite lavas are likelyto reach augite saturation before Ca-poor pyroxene saturation,whereas the Arakapas fault zone lavas, which have relativelyless normative diopside and more quartz, reached the Ca-poorpyroxene-olivine reaction surface and crystallized Ca-poor pyroxeneafter olivine.     

Crystal Accumulation and Magma Mixing in the Petrogenesis of Tholeiitic Andesites from Fukujin Seamount, Northern Mariana Island Arc

Fukujin Seamount is a large, active, submarine volcano on thevolcanic front in the northernseamount province (NSP) of theMariana island arc (MIA). Five dredge hauls from the summitand upper flanks of Fukujin recovered mainly highly porphyriticbasaltic andesites. A few nearly aphyric samples are medium-Ksiliceous andesites (SiO₂ = 62%, K₂O = 1•5%). Fukujin andmost other large arc-front volcanoes of the northern MIA havetholeiitic (iron-enrichment) fractionation trends. This contrastswith the calc-alkaline trends of many smaller seamounts. A negativecorrelation of modal plagioclase content with bulk-rock SiO₂,as well as bulk-rock major and trace element variation trends,and glass analyses, suggests that lavas with >30 vol.% phenocrystsand <55 wt.% SiO₂ are partial cumulates. The presence ofbimodal phenocryst populations along with reversed to normalzoning of phenocrysts is explained by magma mixing of andesiticand basaltic liquids. Hybrid basaltic andesites probably formedby the accumulation of plagioclase in a tholeiitic magma chamberundergoing replenishment and mixing at a shallow crustal level.A petrogenetic model is presented for the origin of basalticandesite by combined magma mixing and fractional crystallization.Aphyric siliceous andesites can be modelled by simple fractionationof basaltic andesite. The early fractionating assemblage consistedmainly of plagioclase and clinopyroxene, with lesser olivineand minor magnetite, but plagioclase remained suspended in themelt. The later fractionating assemblage was dominated by plagioclasewith orthopyroxene instead of olivine. ^*Present address: 2260 rue Panet, Montreal, Quebec, H2L 3A6, Canada.     

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     

Mineral chemistry of submarine lavas from Hilo Ridge, Hawaii: implications for magmatic processes within Hawaiian rift zones

The crustal history of volcanic rocks can be inferred from the mineralogy and compositions of their phenocrysts which record episodes of magma mixing as well as the pressures and temperatures when magmas cooled. Submarine lavas erupted on the Hilo Ridge, a rift zone directly east of Mauna Kea volcano, contain olivine, plagioclase, augite ±orthopyroxene phenocrysts. The compositions of these phenocryst phases provide constraints on the magmatic processes beneath Hawaiian rift zones. In these samples, olivine phenocrysts are normally zoned with homogeneous cores ranging from ∼ Fo₈₁ to Fo₉₁. In contrast, plagioclase, augite and orthopyroxene phenocrysts display more than one episode of reverse zoning. Within each sample, plagioclase, augite and orthopyroxene phenocrysts have similar zoning profiles. However, there are significant differences between samples. In three samples these phases exhibit large compositional contrasts, e.g., Mg# [100 × Mg/(Mg+Fe⁺²)] of augite varies from 71 in cores to 82 in rims. Some submarine lavas from the Puna Ridge (Kilauea volcano) contain phenocrysts with similar reverse zonation. The compositional variations of these phenocrysts can be explained by mixing of a multiphase (plagioclase, augite and orthopyroxene) saturated, evolved magma with more mafic magma saturated only with olivine. The differences in the compositional ranges of plagioclase, augite and orthopyroxene crystals between samples indicate that these samples were derived from isolated magma chambers which had undergone distinct fractionation and mixing histories. The samples containing plagioclase and pyroxene with small compositional variations reflect magmas that were buffered near the olivine + melt ⇒Low-Ca pyroxene + augite + plagioclase reaction point by frequent intrusions of mafic olivine-bearing magmas. Samples containing plagioclase and pyroxene phenocrysts with large compositional ranges reflect magmas that evolved beyond this reaction point when there was no replenishment with olivine-saturated magma. Two of these samples contain augite cores with Mg# of ∼71, corresponding to Mg# of 36–40 in equilibrium melts, and augite in another sample has Mg# of 63–65 which is in equilibrium with a very evolved melt with a Mg# of ∼30. Such highly evolved magmas also exist beneath the Puna Ridge of Kilauea volcano. They are rarely erupted during the shield building stage, but may commonly form in ephemeral magma pockets in the rift zones. The compositions of clinopyroxene phenocryst rims and associated glass rinds indicate that most of the samples were last equilibrated at 2–3 kbar and 1130–1160 °C. However, in one sample, augite and glass rind compositions reflect crystallization at higher pressures (4–5 kbar). This sample provides evidence for magma mixing at relatively high pressures and perhaps transport of magma from the summit conduits to the rift zone along the oceanic crust-mantle boundary. Received: 8 July 1998 / Accepted: 2 January 1999     

Petrology of middle proterozoic diabases and picrites from Lake Nipigon,Canada

Mafic rocks at Lake Nipigon provide a record of rift-related continental basaltic magmatism during the Keweenawan event at 1109 Ma. The mafic rocks consist of an early, volumetrically minor suite of picritic intrusions varying in composition from olivine gabbro to peridotite and a later suite of tholeiitic diabase dikes, sheets and sills. The diabase occurs primarily as two 150 to 200 m thick sills with a textural stratigraphy indicating that the sills represent single cooling units. Compositional variation in the sills indicates that they crystallized from several magma pulses.The diabases are similar in chemistry to olivine tholeiite flood basalts of the adjacent Keweenawan rift, particularly with respect to low TiO₂, K₂O and P₂O₅. The picrites have higher TiO₂, K₂O and P₂O₅ than the diabases and are similar to, but more primitive than, high Fe-Ti basalts which erupted early in the Keweenawan volcanic sequence.All of the rocks crystallized from fractionated liquids. The picrites are cumulate rocks derived at shallow crustal depths from a magma controlled predominantly by olivine fractionation. Picritic chills are in equilibrium with olivine phenocrysts of composition Fo₈₀ and are interpreted to represent the least evolved liquids observed. The parental magma of the picrites was probably Fe rich relative to the parental magma of the diabase. The diabase sills crystallized from an evolved basaltic liquid controlled by cotectic crystallization of plagioclase and lesser olivine and pyroxene.The emplacement of dense olivine phyric picritic magmas early in the sequence, followed by later voluminous compositionally evolved magmas of lower density suggests the development of a crustal density filter effect as the igneous event reached a peak. Delamination of the crust-mantle interface may have resulted in the transition from olivine controlled primitive magma to fractionated magma through the development of crustal underplating.     

准噶尔盆地老山沟火山岩晶体粒度分布及其结晶动力学意义

摘　 要　 阐述了火山岩晶体粒度分布的基本原理和研究方法‚分析了老山沟火山岩斜长石、 辉石、橄榄石、铁钛氧化物的晶体粒度分布。前3种矿物在中间粒度处发生了有意义的弯折‚ 原因是岩浆上升时过冷度增大。估算了岩浆房中斜长石、橄榄石的成核速率、结晶时间及上 升过程中处于结晶带的时间。研究表明‚在岩浆的演化过程中‚晶体的分离和累积作用及岩 浆的混合和对围岩的同化作用可以忽略。     

Petrology of the Treknattan intrusion in the Fongen-Hyllingen complex, Trondheim region, Norway: a late intrusion into an evolved layered complex

The basic-ultrabasic Treknattan intrusion is an important example of a late intrusion in a solidified, evolved, layered complex and sheds light on possible mechanisms by which such associations may develop. The Treknattan intrusion, emplaced into the basic Fongen-Hyllingen intrusion shortly after the latter had solidified, consists mainly of massive or weakly layered peridotite (olivine ± Cr-spinel cumulate) and troctolite (plagioclase + olivine ± Cr-spinel cumulate). The mineral compositional range partially overlaps the most primitive end of the much larger variation-interval in the Fongen-Hyllingen intrusion. The margin of the Treknattan intrusion is sometimes outlined by massive feldspathic websterite which appears to have formed by reaction between magma and melts of gabbroic country rock. The parental magma appears to have been a relatively water-rich picritic basalt with a possible genetic relationship to the magma parental to the enveloping Fongen-Hyllingen intrusion, both displaying tholeiitic relationship between olivine and Ca-poor pyroxene, and having crystallized from relatively water-rich magmas with an early crystallization order of olivine ± Cr-spinel-plagioclase-Ca-rich pyroxene. The recognition of the Treknattan intrusion as a separate body suggests that the bulk composition of the Fongen-Hyllingen intrusion is dioritic rather than gabbroic as previously thought.     

Cyclicity in the Main and Upper Zones of the Bushveld Complex, South Africa: Crystallization from a Zoned Magma Sheet

The major element composition of plagioclase, pyroxene, olivine,and magnetite, and whole-rock ⁸⁷Sr/⁸⁶Sr data are presented forthe uppermost 2·1 km of the layered mafic rocks (upperMain Zone and Upper Zone) at Bierkraal in the western BushveldComplex. Initial ⁸⁷Sr/⁸⁶Sr ratios are near-constant (0·7073± 0·0001) for 24 samples and imply crystallizationfrom a homogeneous magma sheet without major magma rechargeor assimilation. The 2125 m thick section investigated in drillcore comprises 26 magnetitite and six nelsonite (magnetite–ilmenite–apatite)layers and changes up-section from gabbronorite (An₇₂ plagioclase;Mg# 74 clinopyroxene) to magnetite–ilmenite–apatite–fayaliteferrodiorite (An₄₃; Mg# 5 clinopyroxene; Fo₁ olivine). The overallfractionation trend is, however, interrupted by reversals characterizedby higher An% of plagioclase, higher Mg# of pyroxene and olivine,and higher V₂O₅ of magnetite. In the upper half of the successionthere is also the intermittent presence of cumulus olivine andapatite. These reversals in normal fractionation trends definethe bases of at least nine major cycles. We have calculateda plausible composition for the magma from which this entiresuccession formed. Forward fractional crystallization modelingof this composition predicts an initial increase in total iron,near-constant SiO₂ and an increasing density of the residualmagma before magnetite crystallizes. After magnetite beginsto crystallize the residual magma shows a near-constant totaliron, an increase in SiO₂ and decrease in density. We explainthe observed cyclicity by bottom crystallization. Initiallymagma stratification developed during crystallization of thebasal gabbronorites. Once magnetite began to crystallize, periodicdensity inversion led to mixing with the overlying magma layer,producing mineralogical breaks between fractionation cycles.The magnetitite and nelsonite layers mainly occur within fractionationcycles, not at their bases. In at least two cases, crystallizationof thick magnetitite layers may have lowered the density ofthe basal layer of melt dramatically, and triggered the proposeddensity inversion, resulting in close, but not perfect, coincidenceof mineralogical breaks and packages of magnetitite layers. KEY WORDS: layered intrusion; mineral chemistry; isotopes; magma; convection; differentiation     

Abyssal tholeiites from the Oceanographer Fracture Zone

Unusual effects have been discovered in the major element phase relations of basalts from the Oceanographer Fracture Zone (OFZ) which suggest that magma mixing of primitive basalt with the differentiation residue of a previous batch of primitive magma has occurred. These effects include a reversal in mineral crystallization sequence which cannot happen during normal differentiation processes or be explained by any plausible change in physical conditions. This unusual effect is encountered as a result of curvature in composition space of the liquid-line-of-descent equilibria involving olivine, plagioclase, and high-calcium clinopyroxene. Mixing of magmas at different stages of their evolution produces mixtures that do not lie on the curved liquid-line-of-descent. Observation of such anomalous compositions in the OFZ suite supplements accumulating petrographic and trace-element geochemistry evidence that magma mixing is an important petrogenetic process. Mixing of fractionated residual liquids can produce mixtures which are either superheated or supercooled depending on the sense of ‘thermal curvature’ of the liquid-line-of-descent. Both senses are encountered in the tholeiitic system, and this effect may exert a qualitative control on the crystallization texture of the mixture. A comparison of approximately 2,000 abyssal tholeiite compositions to the experimental liquid-line-of-descent reveals that erupted differentiates which would be expected from advanced fractionation are scarce. Just this sort of phenomenon (the ‘perched’ steady state) was proposed by O'Hara (1977) as an earmark of the operation of a continuously fractionating magma chamber into which fresh magma is periodically remixed.     

Textural and compositional evidence for magma mixing and its mechanism,Abu volcano group,southwestern Japan

Quaternary basalts, andesites and dacites from the Abu monogenetic volcano group, SW Japan, (composed of more than 40 monogenetic volcanoes) show two distinct chemical trends especially on the FeO^*/MgO vs SiO₂ diagram. One trend is characterized by FeO^*/MgO-enrichment with a slight increase in SiO₂ content (Fe-type trend), whereas the other shows a marked SiO₂-enrichment with relatively constant FeO^*/MgO ratios (Si-type trend). The Fe-type trend is explained by fractional crystallization with subtraction of olivine and augite from a primitive alkali basalt magma. Rocks of the Si-type trend are characterized by partially melted or resorbed quartz and sodic plagioclase phenocrysts and/or fine-grained basaltic inclusions. They are most likely products of mixing of a primitive alkali basalt magma containing olivine phenocrysts with a dacite magma containing quartz, sodic plagioclase and hornblende phenocrysts. Petrographic variation as well as chemical variation from basalt to dacite of the Si-type trend is accounted for by various mixing ratios of basalt and dacite magmas. Pargasitic hornblende and clinopyroxene phenocrysts in andesite and dacite may have crystallized from basaltic magma during magma mixing. Olivine and spinel, and quartz, sodic plagioclase and common hornblende had crystallized in basaltic and dacitic magmas, respectively, before the mixing. Within a lava flow, the abundance of basaltic inclusions decreases from the area near the eruptive vent towards the perimeter of the flow, and the number of resorbed phenocrysts varies inversely, suggesting zonation in the magma chamber.The mode of mixing changes depending on the mixing ratio. In the mafic mixture, basalt and dacite magmas can mix in the liquid state (liquid-liquid mixing). In the silicic mixture, on the other hand, the basalt magma was quenched and formed inclusions (liquid-solid mixing). During mixing, the disaggregated basalt magma and the host dacite magma soon reached thermal equilibrium. Compositional homogenization of the mixed magma can occur only when the equilibrium temperature is sufficiently above the solidus of the basalt magma. The Si-type trend is chemically and petrographically similar to the calc-alkalic trend. Therefore, a calc-alkalic trend which is distinguished from a fractional crystallization trend (e.g. Fe-type trend) may be a product of magma mixing.     

Petrographic and Geochemical Evidence for Magma Mixing and Crustal Contamination in the Post-Collisional Calc-Alkaline Yozgat Volcanics,Central Anatolia,Turkey

Petrographic, major-oxide, and trace-element data are presented for the Yozgat volcanics. These rocks range in composition from basalts through basaltic andesites and andesites to dacites. Major-oxide variations are largely explicable in terms of fractional crystallization, involving removal of observed phenocrysts and microphenocrysts. However, complex zoning patterns and resorbtion phenomena shown by phenocrysts in these lavas, and observed epitaxitic pyroxene growth around quartz xenocrysts imply that they are hybrids formed by a mixing process. In addition, observed enrichments in crustal elements such as K, Rb, Ba, Sr, and P provide clear evidence for the crustal assimilation of granitoid and metasedimentary xenoliths. The following model is suggested for the evolution of the Yozgat volcanics. The primitive magma underwent fractionation in an intracrustal magma chamber to yield more evolved liquids. Influx of hot, primitive magma into the magma chamber promoted vigorous convection-crustal assimilation and eruption of the volcanic rocks in the study area.     

Contrasting compositional trends of rocks and olivine-hosted melt inclusions from Cerro Negro volcano (Central America): implications for decompression-driven fractionation of hydrous magmas

Melt inclusions in olivine Fo_83–72 from tephras of 1867, 1971 and 1992 eruptions of Cerro Negro volcano represent a series of basaltic to andesitic melts of narrow range of MgO (5.6–8 wt %) formed by ~46 wt % fractional crystallization of olivine (~6 wt %), plagioclase (~27 wt %), pyroxene (~13 wt %) and magnetite (<1 wt %) from primitive basaltic melt (average SiO₂ = 49 wt %, MgO = 7.6 wt %, H₂O = 6 wt %) as it ascended to the surface from the depth of about 14 km. The crystallization occurred at increasing liquidus temperature from 1,050 to 1,090 °C in the pressure range from 400 to 50 MPa and was induced by release of mixed H₂O–CO₂ fluid from the melt at decreasing pressure. Matrix glass compositions fall at the high-Si end of the melt inclusion trend and represent the final stage of melt crystallization during and after eruption. The bulk compositions of erupted Cerro Negro magmas (tephras and lavas) range from high- to low-MgO (3–10 wt %) basalts, which form a compositional array crossing the trend of melt inclusions so that virtually no rock from Cerro Negro has composition akin to true melt represented by the inclusions. The variations of the bulk magma (rocks) and melt (melt inclusions) compositions can be generated in a dyke connecting a deep primitive magma reservoir with the Cerro Negro edifice. While the melt inclusions represent the compositional trend of instantaneous melts along the magma pathway at decreasing pressure and H₂O content, occurrence of low-Mg to high-Mg basalts reflects the process of phenocryst re-distribution in progressively evolving melt. The crystallization scenario is anticipated to operate everywhere in dykes feeding basaltic volcanoes and can explain the predominance of plagioclase-rich high-Al basalts in island arc as well as typical compositional variations of magmas during single eruptions.     

Petrology and petrogenesis of a tertiary bimodal dolerite-peralkaline/subalkaline trachyte/rhyolite dyke association from Lundy,Bristol Channel,UK

The island of Lundy forms the southernmost igneous complex of the British Tertiary Volcanic Province (BTVP) and consists of granite (≈ 90%) emplaced into deformed Devonian sedimentary rocks (Pilton Shale) and associated with a swarm of dykes of dolerite/basalt, minor trachyte and rhyolite composition. The dolerites are of varied olivine basalt composition and are associated with peralkaline trachyte and subalkaline/peralkaline rhyolite with alkali feldspar and quartz ± alkali amphibole ± pyroxene mineralogy. The dyke swarm is therefore an anorogenic bimodal dolerite/basalt–trachyte/rhyolite BTVP association. Although the dyke association is bimodal in major element terms between dolerite/basalt and minor trachyte/rhyolite, the mineralogy and trace element geochemistry indicate that the dykes may be regarded as a cogenetic dolerite—peralkaline trachyte/rhyolite association with minor subalkaline rhyolites. Sr and Nd isotope data indicate derivation of these magmas from a similar BTVP mantle source (with or without minor contamination by Pilton Shale, or possibly Lundy granite). The petrogenesis of the Lundy dyke association is therefore interpreted in terms of extensive fractional crystallization of basaltic magma in a magma chamber of complex geometry below the (exposed) Lundy granite. Fractional crystallization of a representative dolerite magma (olivine ± clinopyroxene ± plagioclase) yields trachyte magma from which the crystallization of alkali feldspar (anorthoclase) ± plagioclase (oligoclase) + Fe–Ti oxide + apatite results in peralkaline rhyolite. Rarer subalkaline rhyolites result from fractionation from a similar dolerite source which did not achieve a peralkaline composition so allowing the crystallization and fractionation of zircon. The basalt–(minor trachyte)/rhyolite bimodality reflects rapid crystallization of basalt magma to trachyte (and rhyolite) over a relatively small temperature interval (mass fraction of melt, F = ≈ 0.15). The rapid high level emplacement of basalt, trachyte and rhyolite dyke magmas is likely to have been associated with the development of a substantial composite bimodal basalt–(minor trachytel)/rhyolite volcano above the BTVP Lundy granite in the Bristol Channel.     

吉林红旗岭1号和7号岩体中含矿超镁铁质岩的矿物化学特征:对岩浆演化过程以及铜镍硫化物矿床形成机制的约束

本文对吉林红旗岭1号和7号岩体中含矿超镁铁质岩的主要造岩矿物进行了详细研究。两岩体的主要造岩矿物为贵橄榄石、古铜辉石、单斜辉石、斜长石、角闪石和金云母。岩浆的暗色矿物结晶顺序为:橄榄石→斜方辉石→单斜辉石→角闪石→黑云母,与镜下实际观察一致,是岩浆在不同深度结晶的产物。原始岩浆来自上地幔,两岩体进入高位岩浆房中的熔体的MgO含量分别13.98%和14.22%、Mg#值分别为72.22和71.05,为含水的高镁的苦橄质玄武岩浆。深部岩浆房深度距地表约26～27km,岩浆房内的结晶温度介于1280～1379℃之间,即结晶于下地壳中。岩浆由深部上升到高位(浅部)岩浆房中的过程是近绝热的,也是快速完成的。岩浆可能经历了两次岩浆房的演化过程,岩浆在上升到高位岩浆房之前,在深部曾经历了较短时间的橄榄石和少量辉石的分离结晶作用;但在高位岩浆房中混染了地壳物质,与此同时,还经历了同源岩浆混合作用以及岩浆过冷却作用,这些都有利于岩浆体系中成矿元素含量增高以及硫达到饱和状态,使金属硫化物熔离并晶出,从而使岩体发生铜镍矿化作用。     

西昆仑普鲁新生代火山岩的矿物化学特征及其对岩浆演化过程的约束

对西昆仑普鲁新生代火山岩的矿物学进行了系统的研究。结果表明：该地区火山岩主要由橄榄石、单斜辉石和斜长石组成,并有少量的斜方辉石、黑云母、角闪石、碱性长石和铁钛氧化物。其矿物学特征指示了岩浆的性质有点类似于碱性岩浆,但与典型的碱性玄武岩又有明显的区别,属于橄榄安粗岩系列。利用橄榄石-熔体平衡原理估算了进入高位岩浆房中的熔体的MgO含量约为6．2％,Mg^#为0．57,说明其不是地幔熔融形成的原始岩浆,而是经历了深部岩浆房的分离结晶过程。由单斜辉石估算的高位岩浆房的深度约7～9km。岩浆在高位岩浆房中发生了较长时间的强烈分离结晶作用,分离结晶相主要为橄榄石、单斜辉石和斜长石以及少量的斜方辉石、黑云母、角闪石、碱性长石和铁钛氧化物。不同时期形成的铁钛氧化物指示了分离结晶过程由相对高温高氧逸度向相对低温低氧逸度演化。与此相对照的是岩浆在深部岩浆房中可能只发生了橄榄石和辉石等铁镁矿物的分离结晶作用,且分异作用时间较短。深部岩浆房可能存在于岩石圈地幔或壳幔过渡带中,岩浆由深部岩浆房上升到高位岩浆房中的过程是近绝热的,从浅部岩浆房到地表是快速上升的过程。     

Enrichment of basalt and mixing of dacite in the rootzone of a large rhyolite chamber: inclusions and pumices from the Rattlesnake Tuff, Oregon

 A variety of cognate basalt to basaltic andesite inclusions and dacite pumices occur in the 7-Ma Rattlesnake Tuff of eastern Oregon. The tuff represents ∼280 km³ of high-silica rhyolite magma zoned from highly differentiated rhyolite near the roof to less evolved rhyolite at deeper levels. The mafic inclusions provide a window into the processes acting beneath a large silicic chamber. Quenched basaltic andesite inclusions are substantially enriched in incompatible trace elements compared to regional primitive high-alumina olivine tholeiite (HAOT) lavas, but continuous chemical and mineralogical trends indicate a genetic relationship between them. Basaltic andesite evolved from primitive basalt mainly through protracted crystal fractionation and multiple cycles (≥10) of mafic recharge, which enriched incompatible elements while maintaining a mafic bulk composition. The crystal fractionation history is partially preserved in the mineralogy of crystal-rich inclusions (olivine, plagioclase ± clinopyroxene) and the recharge history is supported by the presence of mafic inclusions containing olivines of Fo₈₀. Small amounts of assimilation (∼2%) of high-silica rhyolite magma improves the calculated fit between observed and modeled enrichments in basaltic andesite and reduces the number of fractionation and recharge cycles needed. The composition of dacite pumices is consistent with mixing of equal proportions of basaltic andesite and least-evolved, high-silica rhyolite. In support of the mixing model, most dacite pumices have a bimodal mineral assemblage with crystals of rhyolitic and basaltic parentage. Equilibrium dacite phenocrysts are rare. Dacites are mainly the product of mingling of basaltic andesite and rhyolite before or during eruption and to a lesser extent of equilibration between the two. The Rattlesnake magma column illustrates the feedback between mafic and silicic magmas that drives differentiation in both. Low-density rhyolite traps basalts and induces extensive fractionation and recharge that causes incompatible element enrichment relative to the primitive input. The basaltic root zone, in turn, thermally maintains the rhyolitic magma chamber and promotes compositional zonation. Received: 1 June 1998 / Accepted: 5 February 1999     

Magma influx and mixing in the Bjerkreim-Sokndal layered intrusion, South Norway: evidence from the boundary between two megacyclic units at Storeknuten

The Bjerkreim-Sokndal layered intrusion belongs to the Proterozoic anorthositic province in the Rogaland area of southern Norway. The northwestern part of the intrusion comprises a ca. 6 km-thick Layered Series made up of megacyclic units (MCU) arranged in a syncline; each megacyclic unit reflects the influx of fresh magma into the chamber. The boundary between megacyclic units III and IV has been studied in detail at Storeknuten on the southern flank of the syncline. The megacyclic units can be subdivided into a series of cumulate stratigraphic zones; the interval from the top of zone IIIe to the base of zone IVd is exposed in the Storeknuten area. Modally layered plagioclase-hypersthene-ilmenite-magnetite-augite-apatite cumulates belonging to zone IIIe are overlain by 30 m of massive plagioclase-rich rocks (commonly containing ilmenite and/or hypersthene) constituting zone IVa. The entry of cumulus olivine defines the base of zone IVb (dominantly plagioclase-olivine-ilmenite cumulates) which is about 100 m thick. Many of the olivines are partly or completely replaced by Ca-poor pyroxene/Fe---Ti oxide symplectites. This massive leucotroctolitic zone is overlain by modally layered, laminated plagioclase-hypersthene-ilmenite cumulates of zone IVc. The successive entry of magnetite, apatite (accompanied by Ca-rich pyroxene) and inverted pigeonite defines zones IVd, e and f respectively. The entry of K-feldspar (accompanied by Fe-rich olivine) defines the base of a jotunitic transition zone which passes upwards into mangerites and quartz mangerites.

There is a compositional regression through zone IVa. The upper part of zone IIIe has Ca-poor pyroxene with about En68, plagioclase with An44–48 and a Sr-isotope ratio of about 0.7062, while the base of zone IVb has olivine with Fo75 together with En78, An53 and 0.7050 respectively. Similar reversals are shown by the minor element compositions of plagioclase and Fe---Ti oxides. Sr-isotope ratios increase systematically up through zone IVb (reaching 0.7058 in zone IVd) while An% and Sr in plagioclase and Ni and Cr in Fe---Ti oxides decrease. Olivine compositions vary unsystematically and are believed to have changed their Fe:Mg ratios as a result of trapped liquid shift.

The magma residing in the chamber when the influx at the base of megacyclic unit IV took place was compositionally zoned, and assimilation of gneissic country rock at the roof had resulted in the Sr-isotope ratio increasing up through the magma column. The new magma had a Sr-isotope ratio of about 0.7050 while the resident magma had a ratio of 0.7062 at the floor, increasing upwards. The new magma mixed with the basal layer(s) of the compositionally zoned resident magma and crystallization of this hybrid magma during influx and mixing produced the compositional regression in zone IVa. When magma influx ceased, olivine-bearing rocks began to crystallize at the base of zone IVb. The leucotroctolites at the base of this zone are the most primitive rocks in the entire intrusion. The systematic increase in Sr-isotope ratios up through zone IVb resulted from progressive mixing between new and resident magma. This mixing either took place during magma influx or by the progressive mixing of overlying resident magma layers during crystallization.

Calculations based on geochemical modelling, the thickness of cumulate stratigraphy repeated and Sr-isotope ratios indicate that the new magma influx had a thickness of 350–500 m in the Storeknuten section and that the leucotroctolites of zone IVb represent about 20–30% crystallization of this influx.     

金川Ⅰ号岩体橄榄石Ni-MgO相互关系及其地质意义

金川超镁铁质岩体赋存着仅次于加拿大Sudbury和俄罗斯Noril'sk-Talnakh的世界第三大在采铜镍硫化物矿床,岩体以一系列的NE向断层为界分成四个小岩体,由西至东依次为:Ⅲ、Ⅰ、Ⅱ、Ⅳ岩体.Ⅰ号岩体主要由二辉橄榄岩、含辉橄榄岩和橄榄二辉岩构成,橄榄石在各岩相中均为保存较好的主要造岩矿物.本文研究得到金川Ⅰ号岩体上部二辉橄榄岩和含辉橄榄岩中橄榄石的镁橄榄石F_o值介于83.9～85.7,而其Ni含量为1396×10~(-6)～2043×10~(-6),大多低于从S不饱和玄武岩浆中结晶出来的橄榄石的Ni含量.模拟计算结果表明橄榄石较低的Ni含量是因为橄榄石结晶的同时,发生了强烈的硫化物熔离;橄榄石的Fo-Ni关系还因与晶间硅酸盐熔浆的物质交换而发生改变.模拟计算还证明大约有30%的晶间硅酸盐岩浆与橄榄石发生Fe-Mg物质交换反应,导致早结晶橄榄石的Fo值减少了1～1.5.同时,橄榄石较小的Fo值变化表明,在橄榄石结晶和硫化物熔离过程中,不断有新的岩浆贯入和补充.