Trace element modelling of pelite-derived granites

The presence or absence of a vapour phase during incongruent-melt reactions of muscovite and biotite together with the composition of the protolith determines the trace-element characteristics of the resulting melt, provided that equilibrium melting occurs for those phases that host the tracc elements of interest. For granitic melts, Rb, Sr and Ba provide critical constraints on the conditions that prevailed during melting, whereas REE are primarily controlled by accessory phase behaviour. Mass-balance constraints for eutectic granites that are formed by the incongruent melting of muscovite in pelites indicate that melting in the presence of a vapour phase will result in a large melt fraction, and deplete the restite in feldspar. Hence the melt will be characterized by low Rb/Sr and high Sr/Ba ratios. In contrast, vapour-absent melting will result in a smaller melt fraction, and an increase in the restitic feldspar. Consequently high Rb/Sr and low Sr/Ba ratios are predicted. Vapour-absent melting will also enhance the negative Eu anomaly in the melt. Granites that result from the incongruent melting of biotite in the source will be characterized by higher Rb concentrations than those that result from the incongruent melting of muscovite. The Himalayan leucogranites provide an example of unfractionated, crustally derived eutectic melts that are enriched in Rb but depleted in Sr and Ba relative to their metasedimentary protoliths. These compositions may be generated by the incongruent melting of muscovite as a low melt fraction (F0.1) from a pelitic source under vapour-absent conditions.     

Trace element modelling of the origin and evolution of the Oyaca‐Boyalik volcanic rocks (NE of Haymana,Ankara, Turkey)

Lower Miocene Boyalik volcanic rocks, situated approximately 80 km south of Ankara, exhibit both alkaline and calc‐alkaline characteristics. Alkaline products are trachybasaltic and trachyandesitic, whereas calc‐alkaline products are dacitic. The phenocrysts in the dacites consist primarily of plagioclase and hornblende, with lesser amounts of biotite. The groundmass contains plagioclase and quartz microcrysts. Trachyandesites are mainly composed of plagioclase and biotite phenocrysts with a groundmass of alkali feldspar microlites and minor clinopyroxene microcrysts. Trachybasalts are mainly composed of olivine and plagioclase phenocrysts, with minor clinopyroxene phenocrysts associated with alkali feldspar, plagioclase and clinopyroxene microlites and microcrysts in the groundmass. Oxides are common accessory phases in all products. Boyalik volcanic rocks have essentially homogeneous incompatible trace element patterns with variable Nb and Th anomalies, enrichment in Rb, Ba, K, La, Ce and Nd, and positive Sr anomalies. Some trace element ratios (e.g. Ba/Ta, Ba/Nb, Th/U and Ce/Pb) are variable among the series. For instance, dacites and trachyandesites have higher Ba/Ta (724–2509), Ba/Nb (45–173) and Th/U (3.5–8.7) and lower Ce/Pb (7.1–3.9) values than the trachybasalts. Trace element data indicate that the series are chemically distinct but probably were derived from a common lithospheric mantle source via variable degrees of partial melting. The magmas then underwent a process of evolution involving assimilation and fractional crystallization (AFC) during ascent to the surface. Although trachyandesites and dacites were generated from a lithospheric mantle source via ～1% and ～1.5% to ～5% degrees of partial melting, respectively, trachybasalts were derived from the same source via higher degrees of partial melting (～20%) with neglegible crustal contamination. Boyalik volcanism is linked to an intracontinental transpressional setting. However, the overall geochemical features are consistent with derivation from a mantle source that records earlier Eocene subduction between the Sakarya continental fragment and the K?r?ehir block during time.     

Geochemical constraints on crustal anatexis: a case study from the Pan-African Damara granitoids of Namibia

 Major and trace element models of recently published vapour-absent mica dehydration melting experiments are used to identify granitoids generated by muscovite and biotite dehydration melting, and to distinguish between plagioclase-limited and biotite-limited, biotite dehydration melting. In the case of granitoids from the Pan-African Damara mobile belt (Namibia), many of the leucogranites and Salem-type granitoids may be modelled by biotite dehydration melting. The low Rb/Sr granitoids (e.g. Donkerhuk Onanis, Salem Onanis, Donkerhuk Nomatsaus, Salem Goas) probably reflect feldspar-limited, biotite dehydration melting (a pelitic source) whereas the high Rb/Sr suites (e.g. Bloedkoppie leucogranite, Stinkbank leucogranite, Salem Swakopmund, Leucocratic Stink bank granite) reflect biotite-limited, biotite dehydration melting (a greywacke source). Alaskites from the Damara belt have major element compositions which are consistent with muscovite dehydration melting, and their positive Eu anomalies are linked to high K₂O reflecting K-feldspar entrainment. Combined Zr and LREE (light rare earth element) solubility models indicate that insufficient time (probably less than 10⁴ years) had elapsed between melt generation and melt extraction to ensure that the alaskite melts attained their equilibrium concentrations of Zr and the LREEs. In contrast, the leucogranites and Salem-type granites have attained their equilibrium inventories of these trace elements. Combined Fe₂O₃ and MgO contents in some samples from two granitoids (the Salem Goas and Donkerhuk Onanis intrusions) are higher than those readily attainable by biotite dehydration melting indicating either: (1) that they contain a contribution from melts generated by incipient garnet breakdown or; (2) that they contain small amounts of an entrained ferromagnesian phase. Received: 24 April 1995/Accepted: 11 December 1995     

The Petrology of Some Vitrophyric Calc-Alkaline Volcanics from the Carboniferous of New South Wales

The paper deals with the petrography, mineralogy, chemistry,and genesis of selected calcalkaline volcanics from the Carboniferousof New South Wales. The investigated rocks, mainly vitrophyrictypes, range in composition from hypersthene basalt throughhypersthene-augite dacite and ignimbritic hypersthene-hornblendedacite to ignimbrific biotite rhyodacite. Chemical and opticaldata are provided for the principal phenocryst phases whichinclude hypersthene, augite, iron-titanium oxides (cation-deficientspinels and ilmenite), hornblende, biotite, plagioclase, and,more rarely, alkali feldspar. The available data do not favourthe derivation of the dacites from basaltic magma by low pressurefractional crystallization, sialic contamination, or mixingof magmas. The origin of these rocks, particularly the hypersthene-augitedacites, has been referred to the Green-Ring wood model of drypartial melting of high-alumina quartz ecologite in the uppermantle. The chemistry of whole rock groundmass pairs indicatesthat some of the more salic eruptives can be interpreted aslow pressure differentiates of dacitic parental melts. A characteristicfeature of the more mafic volcanics is their pronounced modaland normative excess of hypersthene over augite. The early andextensive precipitation of orthopyroxene from strongtly hypersthenenormativemafic and intermediate liquids relatively low in Fe and Mg playedan important role in maintaining the calc-alkaline characterof derivative liquids.     

Coupling of anatectic reactions and dissolution of accessory phases and the Sr and Nd isotope systematics of anatectic melts from a metasedimentary source

Advances in field observations and experimental petrology on anatectic products have motivated us to investigate the geochemical consequences of accessory mineral dissolution and nonmodal partial melting processes. Incorporation of apatite and monazite dissolution into a muscovite dehydration melting model allows us to examine the coupling of the Rb-Sr and Sm-Nd isotope systems in anatectic melts from a muscovite-bearing metasedimentary source. Modeling results show that (1) the Sm/Nd ratios and Nd isotopic compositions of the melts depend on the amount of apatite and monazite dissolved into the melt, and (2) the relative proportion of micas (muscovite and biotite) and feldspars (plagioclase and K-feldspar) that enter the melt is a key parameter determining the Rb/Sr and ⁸⁷Sr/⁸⁶Sr ratios of the melt. Furthermore, these two factors are not, in practice, independent. In general, nonmodal partial melting of a pelitic source results in melts following one of two paths in ε_Nd-⁸⁷Sr/⁸⁶Sr ratio space. A higher temperature, fluid-absent path (Path 1) represents those partial melting reactions in which muscovite/biotite dehydration and apatite but not monazite dissolution play a significant role; the melt will have elevated Rb/Sr, ⁸⁷Sr/⁸⁶Sr, Sm/Nd, and ε_Nd values. In contrast, a lower temperature, fluid-fluxed path (Path 2) represents those partial melting reactions in which muscovite/biotite dehydration plays an insignificant role and apatite but not monazite stays in the residue; the melt will have lower Rb/Sr, ⁸⁷Sr/⁸⁶Sr, Sm/Nd, and ε_Nd values than its source. The master variables controlling both accessory phase dissolution (and hence the Sm-Nd system), and melting reaction (and hence the Rb-Sr systematics) are temperature and water content. The complexity in Sr-Nd isotope systematics in metasediment-derived melts, as suggested in this study, will help us to better understand the petrogenesis for those granitic plutons that have a significant crustal source component.     

The petrogenesis of topaz rhyolites from the western United States

High-silica topaz-bearing rhyolites of Cenozoic age are widely distributed across the western USA and Mexico. They are characteristically enriched in fluorine (>0.2 wt.%) and incompatible lithophile elements (e.g. Li, Rb, Cs, U, Th, Be). In addition to topaz, the rhyolites contain garnet, bixbyite, pseudobrookite, hematite and fluorite in cavities or in their devitrified groundmasses. Magmatic phases include sanidine, quartz, oligoclase and Fe-rich biotite. Allanite, fluorite, zircon, apatite and magnetite occur in most; pyroxene, hornblende, ilmenite and titanite occur in some. The rhyolites crystallized over a wide temperature interval (850° to 600° C) at \(f_{0_2 } \) that ranges from QFM to NNO. The REE patterns of most topaz rhyolites are almost flat (La/Yb_N=1 to 3) and have deep Eu anomalies (Eu/Eu^*=0.01 to 0.02). Both parameters decrease with differentiation. Titanite-bearing rhyolites have prominent middle REE depletions. Topaz rhyolites appear to have evolved from partial melts of a residual granulitic source in the Precambrian lower crust. According to the proposed model, the passage of hot mafic magmas through the crust produced partial melts as a result of the decomposition of F-rich biotite or amphibole. An extensional tectonic setting allowed these small batches of magma to rise without substantial mixing with contemporaneous mafic magmas. Some of the compositional differences between topaz rhyolites and peralkaline rhyolites may be attributed to the accumulation of fluorine and fluorphile elements (Al, Be, Li, Rb, U, Th, HREE) in melts which give rise to topaz rhyolites and chlorine and chlorophile elements (Ti, Fe, Mn, Zn, Zr, Nb and LREE) in melts which yield peralkaline rhyolites. Hence the F/Cl ratio of the melt or its source may determine the alumina saturation of the magma series. Topaz rhyolites are distinguishable from calc-alkaline rhyolites by lower Sr, Ba, Eu and higher F, Rb, U and Th. The usually low La/Yb ratios of topaz rhyolites distinguish them from both peralkaline and calc-alkaline rhyolite suites.     

碳酸岩岩浆演化的指示性矿物—环带金云母——以山东西部雪野碳酸岩为例

山东西部莱芜－淄博地区的中生代雪野碳酸岩中发育有大量罕见的反环带云母，云母的电子探针分析表明，云母斑晶的核心为黑云母，过渡带和边缘是金云母，基质中云母为金云母，核心黑云母与过渡带的金云母界限清晰，成分突变以及核心黑云母的溶蚀结构表明，核心黑云母和过渡带与边缘带金云母不是同一岩浆体系结晶的产物，核心黑云母可能是碳酸岩岩浆捕获的外来黑云母，过渡带与边缘带金云母同基质中金云母具有相似的化学成分，从过渡带到边缘带，金云母的Mg(Mg Fe)逐渐降低，反映了碳酸岩岩浆的不断结晶演化过程，TiO2的不断降低，一方面是由于岩浆的分异结晶，另一方面则是岩浆上升期间去气作用导致岩浆内CO2／H2O值降低所致。云母斑晶从过渡带向边缘带Al2O3含量逐渐减少，表明碳酸岩浆自过渡带云母结晶后没有富Al的圈岩物质加入。     

Large-ion lithophile element characteristics of an amphibolite facies to granulite facies transition at Gruinard Bay, North-west Scotland

Abstract Lewisian grey gneisses from Gruinard Bay, North-west Scotland retain mineralogical and geochemical evidence for Scourian horn-blende-granulite facies metamorphism, and they may be used to assess current models of elemental depletion at granulite grade. Their 'immobile'major and trace element geochemistry is indistinguishable from that of Lewisian amphibolite and pyroxene-granulite facies counterparts. The K, Rb, Th and U contents of the Gruinard Bay gneisses are depleted relative to amphibolite facies gneisses, but generally the abundances of these elements are above those of comparable pyroxene granulites. U and Th have reached an advanced stage of depletion, but allanite appears to be crucial in maintaining significantly higher U and Th abundances at Gruinard Bay than in pyroxene granulites. K and Rb loss is less extreme, and depends on the stability of the rock-forming minerals: K-feldspar; biotite; and, amphibole. Early removal of K and Rb has resulted in a small rise in K/Rb, but further preferential Rb loss would have been required to generate the characteristically high K/Rb ratios of Lewisian pyroxene granulites.
The residence of U and Th in the accessory minerals of granulite facies gneisses, which are often correlated with the residua of intracrustal partial melting, renders unlikely their extreme incompatibility required by such models. Even if such phases are ignored, high mineral-melt partition coefficients for silicic melts argue against partial fusion as an efficient depletion mechanism. On the other hand, the advanced stage of U and Th depletion reached in Gruinard Bay gneisses, which were still partly hydrous, severely restricts the role played by CO₂-dominated fluids and a hydrous medium is preferred.     

Age and strontium‐isotope geochemistry of differentiated rocks from the newer Volcanics,MT Macedon Area,Victoria, Australia

The Newer Volcanics Province of Victoria and South Australia consists of a major region of mainly alkaline basalts within which are two restricted areas containing strongly differentiated flow‐rocks. Typical alkalic basalts from this widespread province have K‐Ar ages from 4.5 to 0.5 m.y. and initial ⁸⁷Sr/⁸⁶Sr ratios from 0.7038 to 0.7045. Contrastingly, in the Macedon area of differentiated lavas, flow compositions range from limburgite to soda trachyte, with K‐Ar ages from 6.8 to 4.6 m.y. and initial ⁸⁷Sr/⁸⁶Sr ratios from 0.7052 to 0.7127. These differentiated rocks therefore are older, and some of them may have been contaminated by reaction with more radiogenic basement rocks during differentiation. Alternatively, the variation in initial Sr‐isotope composition may have resulted from varying isotopic composition of partial melts from the immediate source rocks. The most felsic of the differentiated rocks, soda trachyte, is extremely enriched with Rb relative to Sr; one of the three restricted outcrops of this rock (Camel's Hump) yields a total‐rock Rb‐Sr isochron age of 6.3 ± 0.6 m.y. with an initial ⁸⁷Sr/⁸⁶Sr ratio of 0.7127. K‐Ar sanidine ages reported for the three outcrops of trachyte are identical to each other and to the Rb‐Sr isochron result.     

Chemical interrelationships in a low-pressure granulite terrain in Namaqualand. South Africa,and their bearing on granite genesis and the composition of the lower crust

The results of a chemical study of a suite of low-pressure granulite facies rocks in Namaqualand, South Africa, are reported. The area is underlain by augen gneisses and quartzites, which contain interlayered granular quartz-feldspar rocks (termed ‘granulites’) derived by extensive partial melting of the gneiss. The K/Rb ratio of the gneiss increases from 140 to 250 over a melting interval of 70%: the rate of increase being influenced by the presence of biotite. Simultaneously K/Ba and Rb/Sr decrease from 80 to 25 and from 4 to 0.3, respectively. The partial melts (granulites), which reflect, in part, a cumulate character, have similar K/Rb ratios to the parent gneiss (175) but larger K/Ba (238) and Rb/Sr (5) ratios, due to the retention of Ba and Sr in the residue.Three granites intrude the gneisses. One of these was produced by very advanced partial melting of the gneiss. Continuity of chemical composition suggests that the remaining two granites, although spatially separate, are comagmatic, and evolved by feldspar fractionation during ascent. Lower Sr⁸⁷/Sr⁸⁶ ratio coupled with enrichment of Ba, Sr and Rb in the parent magma of these granites relative to the country rocks precludes local derivation and indicates a lower crustal source rock of intermediate composition.The progressive increase in cafemic character of the gneisses, which is similar to that observed in world granulite terrains as a whole, coupled with intrusive granite which reflects reworking of the lower crust in the area studied, supports a partial melting model for the development of a lower crust of progressively more cafemic composition.     

Distribution and petrogenetic behaviour of trace elements in granitic pegmatite quartz from South Norway

The present study documents that the trace-element distribution in granitic quartz is highly sensitive to CAFC processes in granitic melts. Igneous quartz efficiently records both the origin and the evolution of the granitic pegmatites. Aluminium, P, Li, Ti, Ge and Na in that order of abundance, comprises >95% of the trace elements. Most samples feature >1 ppm of any of these elements. The remnant 5% includes K, Fe, Be, B, Ba and Sr whereas the other elements are present at concentrations lower than the detection limit. Potassium, Fe, Be and Ti are relatively compatible hence obtain the highest concentrations in early formed quartz. Phosphorous, Ge, Li and Al are relatively incompatible and generally obtain the highest concentrations in quartz that formed at lower temperatures from more evolved granitic melts. The Ge/Ti, the Ge/Be, the P/Ge and the P/Be ratios of quartz are strongly sensitive to the origin and evolution of the granitic melts and similarly the Rb/Sr and the Rb/K ratios of K-feldspars may be utilised in petrogenetic interpretations. However, the quartz trace element ratios are better at distinguishing similarities and differences in the origin and evolution of granitic melts. After evaluating the different trace element ratios, the Ge/Ti ratio appears to be most robust during subsolidus processes in the igneous systems, hence probably should be the preferred ratio for analysing and understanding petrogenetic processes in granitic igneous rocks.Editorial responsibility: J. Hoefs     

Contributions to the mineral chemistry of Hawaiian rocks

Feldspar phenocrysts, microphenocrysts, groundmass feldspar, interstitial material of feldspar composition, and residual SiO₂-K₂O-rich glass in 24 rocks of the tholeiitic, alkalic, and nephelinic suites from Haleakala and West Maui volcanoes, Maui, Hawaii, were analyzed quantitatively with the electron microprobe. Rocks studied include tholeiite, olivine tholeiite, oceanite, alkalic olivine basalt, alkalic basalt, hawaiite, mugearite, trachyte, basanite, and basanitoid. Results and conclusions: i) In all rocks studied, An decreases and Or increases from phenocrysts to microphenocrysts to groundmass feldspar to interstitial material of feldspar composition. ii) Phenocrysts occur in rocks of the tholeiitic and alkalic suites and, in spite of differences in bulk rock compositions, overlap in composition. iii) Groundmass feldspar in rocks of the tholeiitic suite are nearly identical in composition; the same is true for rocks of the nephelinic suite. However, in the highly differentiated alkalic suite, groundmass feldspar composition ranges from labradorite to sanidine; i.e. the higher the bulk rock CaO, the higher is the An content, and the higher the bulk K₂O, the higher is the Or content. iv) In general, rocks with phenocrysts have groundmass feldspar less An-rich than those without phenocrysts. v) In rocks of the tholeiitic suite, normative feldspar approaches modal feldspar. However, in rocks of the alkalic and nephelinic suites, normative feldspar, because of the presence of highly alkalic interstitial material and the absence of nepheline in the mode but its presence in the norm, is drastically different from modal feldspar. vi) Hawaiites contain labradorite and not andesine, as per definition, and mugearite contains andesine and not oligoclase, as groundmass feldspar. In fact, when considering phenocrysts and interstitial material of feldspar composition, hawaiites range from bytownite to sanidine and mugearite from andesine to sodic sanidine, but normative feldspar plots in the andesine field for hawaiites and the oligoclase field for mugearite. vii) Rocks of the three suites can be distinguished on the basis of Or and An in groundmass feldspar, the presence of thin rims of groundmass composition of phenocrysts of rocks of the alkalic suite, and the presence of interstitial material of anorthoclase to sanidine composition in rocks of the alkalic and nephelinic suites. iix) Rocks transitional between the tholeiitic and alkalic suites are observed and are characterized by transitional mineral compositions.This paper was first presented as a talk before the 68. Annual Meeting of the Cordilleran Section of the Geological Society of America, Honolulu, Hawaii, March 29–April 1, 1972.     

The metamorphic geology of the Windmill Islands,Antarctica: A preliminary account

Rocks of the Windmill Islands, Antarctica (Lat. 66°S, Long. 110°E) consist of a layered sequence of schists, gneisses, and migmatites (the Windmill Metamorphics) intruded by a charnockite (the Ardery Charnockite) and a porphyritic granite (the Ford Granite), and cut by two swarms of easterly‐trending dolerite dykes.

The rocks have undergone four deformations. The first two produced tight isoclinal folds, the third developed broader less appressed concentric folds, and the last deformation produced gentle warps which plunge steeply southwards.

The metamorphic grade of the Windmill Metamorphics ranges from (i) upper amphibolite facies (sillimanite‐biotite‐orthoclase) in the north, through (ii) biotite‐cordierite‐almandine granulite to (iii) hornblende‐orthopyroxene‐granulite in the south. The boundary between (i) and (ii) above is marked by the incoming ortho‐pyroxene and also the outgoing of sphene, and that between (ii) and (iii) by the outgoing of cordierite. Other metamorphic variations, apparent in the field are (i), the southward colour change of biotite (sepia—>red‐brown) and hornblende (blue‐green—>brown‐green) and (ii) the greater abundance of migmatites and pegmatites in the north of the area.

Major‐element rock chemistry suggests that the pre‐metamorphic nature of the schists and gneisses probably consisted of acid and basic volcanics interbedded with sediments ranging from greywacke‐type sandstones to shales. Partial melting of these rocks is thought to have produced some of the more acidic gneisses of the area.

The abundances of the elements K, Rb, and Th are lower than those of terrains of similar grade elsewhere. This is regarded as reflecting original rock composition. The ratios K/Rb, Th/K, and K/(Rb/Sr), however, are comparable with those from similar terrains elsewhere where K, Rb, and Th enrichment by crustal fractionation has been suggested. This suggests that the Windmill Metamorphics were not derived by retrogression from upper granulite‐facies rocks.     

Leucitites from Gaussberg,Antarctica

Leucitities of probable late Pleistocene age from the extinct volcano of Gaussberg on the coast of East Antarctica consist of microphenocrysts of olivine, diopside, and leucite in a largely glassy groundmass. Their extreme K contents and K/Na ratios, as well as high Rb, Ba, and possibly Ti, are compatible with an origin by small degrees of partial melting of phlogopite-rich mantle below the level of amphibole stability, whereas their enrichment in P, Sr, Zr, Nb, La, Ce, Pb, and Th indicates the presence of minor phases such as apatite in the source material. Although the Mg/(Mg+Fe) values (0.70) and relatively high Ni and Cr contents suggest that the Gaussberg lavas represent near-primary melts, some degree of fractionation involving an aluminous phase (probably garnet) may be necessary to produce liquids with atomic K>Al. Alternatively, an as yet poorly understood process such as wall-rock reaction, liquid immiscibility, or mantle metasomatism may have been a critical factor in the genesis of these unusual rocks.Gaussberg is situated on a passive continental margin and does not appear to be related to any other known area of Cainozoic volcanic activity.     

Crystallization paths of leucite-bearing lavas: Examples from Italy

The salic phases found in leucite-basanites, -trachytes, and -phonolites may be used to portray crystallization in the system NaAlSiO₄-KAlSiO₄-CaAl₂Si₂O₈-SiO₂, the phonolite pentahedron. Only two lavas have been found that contain the assemblage leucite-nepheline-plagioclase-sanidine and liquid, a natural pseudo-invariant assemblage (at 900° C±100) equivalent to the isobaric invariant point of the four component system. The diversity of phases in this group of lavas illustrates the role of halogens in controlling their crystallization paths. Thus the presence of F in the leucite-basanites has stabilized magnesian biotite and suppressed sanidine, as has been found in other basanitic lavas (Brown and Carmichael 1969). The presence of Cl in these same lavas has induced the crystallization of sodalite, which takes the place of nepheline in the groundmass. However in the leucite-trachytes, biotite has suppressed olivine and coexists with sanidine and leucite. The presence of S may produce haüyne at the expense of nepheline, and in general sulphate minerals, which include apatite, have the role in lavas of low silica activity that pyrrhotite plays in liquids of high silica activity. Both pyroxenes and titaniferous magnetites in this suite of lavas are very aluminous. Groundmass crystals of pyroxene may have one-fifth of Si replaced by Al. Other phases which occur occasionally are melanite garnet and a potassium-rich hastingsite, but neither ilmenite nor a sulphide mineral has been found. Phenocryst equilibration temperatures, derived from olivine and Sr-rich plagioclase, are generally in the range from 1,050° C to 1,150° C. The high content of incompatible elements (e.g., K, Ba, Rb, F, Sr, P) in these lavas suggests that they represent a small liquid fraction from a mantle source which possibly contains phlogopite.     

Na,Rb and T1 distributions between phlogopite and sanidine by direct synthesis in a common vapour phase

Using a double-capsule technique, phlogopite and sanidine were equilibrated directly in a common aqueous vapour phase to study the distributions of Na, Rb and T1 at 700°C and 1.5 Kbar. Behaviour of these elements approaches ideality for wt.% concentrations of up to Na = 0.18, Rb = 0.55 and T1 = 0.065 in phlogopite and 0.19, 0.33 and 0.063 respectively in sanidine. The following partition coefficients and K_D values for phlogopite/sanidine were obtained: D (Na) = 0.83, D (Rb) = 2.3 rmand D (T1) = 1.3; K_D(Na/K) = 1.2, K_D(Rb/K) = 3.2 and K_D(T1/K) = 1.8. Although these results are preliminary and in some cases marred by analytical uncertainty, they nevertheless demonstrate the feasibility of the technique as applied to studies of multielement distribution between two or more coexisting solid phases.     

Commingling and mixing of S-type peraluminous, ultrapotassic and basaltic magmas in the Cayconi volcanic field, Cordillera de Carabaya, SE Peru

The Cayconi district of the Cordillera de Carabaya, SE Peru, exposes a remnant of an upper Oligocene–Lower Miocene (22.2–24.4 Ma) volcanic field, comprising a diverse assemblage of S-type silicic and calc-alkaline basaltic to andesitic flows, members of the Picotani Group of the Central Andean Inner Arc. Basaltic flows containing olivine, plagioclase, clinopyroxene, ilmenite and glass, and glassy rhyolitic agglutinates with phenocrystic quartz, cordierite, plagioclase, sanidine, ilmenite and apatite, respectively exhibit mineralogical and geochemical features characteristic of medium-K mafic and Lachlan S-type silicic lavas. Cordierite-bearing dacitic agglomerates and lavas, however, are characterized by dispersed, melanocratic micro-enclaves and phenocrysts set in a fine-grained quartzo-feldspathic matrix. They contain a bimodal mica population, comprising phlogopite and biotite, as well as complexly zoned, sieve-textured plagioclase grains, sector-zoned cordierite, sanidine, quartz, irregular patches of replaced olivine, clinopyroxene and orthopyroxene and accessory phases including zircon, monazite, ilmenite and chromite. The coexistence of minerals not in mutual equilibrium and the growth/dissolution textures exhibited by plagioclase are features indicative of magmatic commingling and mixing. Trachytic-textured andesite flows interlayered with olivine+plagioclase–glomerophyric, calc-alkaline basalts have a phenocrystic assemblage of resorbed orthopyroxene and plagioclase and exhibit melanocratic groundmass patches of microphenocrystic phlogopite, Ca-rich sanidine, ilmenite and aluminous spinel. The mineralogical and mineral chemical relationships in both the dacites and the trachytic-textured andesites imply subvolcanic mixing between distinct ultrapotassic mafic melts, not represented by exposed rock types, and both the S-type silicic and calc-alkaline mafic magmas. Such mixing relationships are commonly observed in the Oligo-Miocene rocks of the Cordillera de Carabaya, suggesting that the S-type rocks in this area and, by extension, elsewhere derive their unusually high K₂O, Ba, Sr, Cr and Ni concentrations from commingling and mixing with diverse, mantle-derived potassic mafic magmas.     

中昆仑造山带钾玄岩质火山岩的地质、地球化学和时代

本文论述了中昆仑(北坡)4个地区第四纪火山岩的地质产状、岩石学、地球化学特征及时代。这一套岩石以安粗岩类为主,普遍含有普通辉石和斜长石斑晶,少数还有橄榄石、紫苏辉石或石英、透长石、黑云母斑晶。在化学上以富碱尤其富钾为突出特点,K₂O/Na₂O≥1,而且 Rb、Sr、Ba 等低场强元素和 LREE 也强烈富集,构成一个连续的钾玄岩系列(Shoshoaite Serics)。区域构造,地球化学和深源捕虏体的证据表明,本区钾玄质岩浆来自于上地幔的低度部分熔融,并受到地壳的同化和污染。火山活动大致从晚第三纪开始一直延续到第四纪,特别是中、晚更新世最为剧烈,是昆仑山及青藏高原快速隆升的新构造运动表现形式之一。     

Trace element behaviour during migmatization. Evidence for a complex melt-residuum-fluid interaction in the St. Malo migmatitic dome (France)

The St. Malo migmatitic dome represents an interesting example wherein migmatites arise from the anatexis of the surrounding gneisses. Petrographical and chemical data suggest that leucosome compositions are compatible with partial melting of the quartzo-feldsphathic fraction of the parent gneiss. The contribution of the incongruent melting of biotite to the melt does not exceed 5% of the parent rock.Petrogenetic modelling based on experimental data and assuming non modal batch melting show that the K, Rb, Ca, Sr, U and Th chemical patterns of these migmatites result in fact from the interaction of several mechanisms, namely: equilibrium partial melting, mixing between melts and refractory minerals (biotite and accessories), melt removal and late hydrothermal alteration. Zr, Y and Th which are mostly hosted in accessory minerals are significantly withheld from the melts and remain stored in melanosomes (metatexites) except when leucosomes are affected by mixing (diatexites). U is frequently enriched in the leucosomes as well as in some melanosomes suggesting external supply.     

中昆仑造山带钾玄岩质火山岩的地质、地球化学和时代

 本文论述了中昆仑(北坡)4个地区第四纪火山岩的地质产状、岩石学、地球化学特征及时代。这一套岩石以安粗岩类为主,普遍含有普通辉石和斜长石斑晶,少数还有橄榄石、紫苏辉石或石英、透长石、黑云母斑晶。在化学上以富碱尤其富钾为突出特点,K₂O/Na₂O≥1,而且 Rb、Sr、Ba 等低场强元素和 LREE 也强烈富集,构成一个连续的钾玄岩系列(Shoshoaite Serics)。区域构造,地球化学和深源捕虏体的证据表明,本区钾玄质岩浆来自于上地幔的低度部分熔融,并受到地壳的同化和污染。火山活动大致从晚第三纪开始一直延续到第四纪,特别是中、晚更新世最为剧烈,是昆仑山及青藏高原快速隆升的新构造运动表现形式之一。