Ordering and exsolution processes in Or-rich alkali feldspar megacrysts from the Eldzhurtinskiy granite (Caucasus)

 The extremely young (2.5 Ma) I-type Eldzhurtinskiy granite complex (Central Caucasus) is uniform with respect to modal composition, major and trace element chemistries of bulk rocks and mineral phases. In contrast, it reveals two types of alkali feldspar megacrysts differing in tetrahedral Al-content (2t₁) and exsolution microtextures: 1. Alkali feldspar megacrysts (Or₇₀An₂Ab₂₈) from the top of the body consist of ideally coherent intergrowths of fine-scale regular Or- and Ab-rich lamellae. The exsolved K-feldspar host is monoclinic (2t₁=0.7), the exsolved Na-rich phase consists of Albite- and/or Pericline-twinned albite. 2. Megacrysts from greater depths have the same bulk composition, but the exsolved Ab-rich phase occurs in the form of optically visible, broad lamellae and patches of low albite. In addition, the K-rich host yields a higher degree of (Al, Si) ordering (2t₁=0.8). The evolution of the distinct types of megacrysts reflects differences in the cooling history within the upper and lower part of the granite body. The occurrence of the coherent lamellae in the megacrysts from the top of the body is attributed to exsolution under dry conditions during fast cooling, whereas coarsening of lamellae and formation of albite patches in the megacrysts from the lower part are caused by fluid-feldspar interaction. The transition zone in the body between the two types of megacrysts is sharp (in a depth interval of 100–200 m) and not related to shear zones. Received: 12 June 1995 / Accepted: 29 January 1996     

Solubility of Ca and Al in orthopyroxene from spinel peridotite: an improved version of an empirical geothermometer

Geothermometric equations for spinel peridotites by Fujii (1976), Gasparik and Newton (1984), and Chatterjee, and Terhart (1985) based on the reaction enstatite (en)+spinel (sp)Mg–Tschermaks (mats)+forsterite (fo) were tested using a nearly isothermal suite of mantle xenoliths from the Eifel, West Germany. In spite of using activities of MgAl₂O₄, en, and mats to allow for the non-ideal solution behaviour of the constituent phases, temperatures calculated from these equations systematically change as a function of Cr/(Cr+AL+Fe³⁺) in spinel. We propose an improved version of the empirical geothermometer for spinel peridotites of Sachtleben and Seck (1981) derived from the evaluation of the solubilities of Ca and Al in orthopyroxene from more than 100 spinel peridotites from the Rhenish Volcanic Province. A least squares regression yielded a smooth correlation between

The origin of glasses in hydrous mantle xenoliths from the West Eifel,Germany: incongruent break down of amphibole

Patches of glass with a second generation of small crystals of olivine, clinopyroxene, and spinel are abundant in hydrous peridotite mantle xenoliths with tabular equigranular textures from two maar-type volcanoes, Meerfelder Maar and Dreiser Weiher (West Eifel, Germany). The patches are similar in size to the main phases of the hosting peridotite. Their central part is often occupied by relics of pargasitic amphibole. Mass-balance calculations show that the patches were formed by surface controlled incongruent thermal breakdown of amphibole according to the reaction: amphibole olivine + clinopyroxene + spinel + melt. Simultaneously with the decomposition of amphibole, small crystals of olivine, clinopyroxene, and spinel grew radially from the patch/peridotite interface toward the centre of the patch. Apart from sector zoning of clinopyroxene, the crystals are virtually homogeneous and are separated from the amphibole by a seam of melt (glass). Secondary olivines reveal higher Mg-numbers, secondary clinopyroxenes higher Cr₂O₃ concentrations than olivines and clinopyroxenes, respectively, of the host peridotite. The silica contents of melts produced by the above breakdown reaction range from 48 to 52% SiO₂ as a function of the composition of the parent amphiboles. Patches surrounded by primary olivines only reveal no reaction with the host peridotite. The variation of SiO₂, MgO and CaO in melts from these patches is the result of minor precipitation of olivine and clinopyroxene during fast cooling. If patches are in contact with primary olivine and orthopyroxene, melts are additionally modified by the reaction liquid 1 + orthopyroxene liquid 2 + olivine + clinopyroxene resulting in more silica-rich compositions between 54 and 58%. For the rare glasses richer in silica, a more complex formation is required. Veinlets along grain boundaries are filled with glasses which are chemically identical to those from nearby patches. This suggests that the veinlets were filled by melts formed by amphibole breakdown during entrainment of the xenoliths to the host magmas.     

Infiltration of refractory melts into the lowermost oceanic crust: evidence from dunite- and gabbro-hosted clinopyroxenes in the Bay of Islands Ophiolite

Up to 3 km of dunitic rocks occur below crustal gabbro in the Blow Me Down massif (Bay of Islands Ophiolite, Newfoundland). Analyses of dunite- and gabbro-hosted clinopyroxene grains (cpx) for rare earth elements (REE), Zr, and Ti reveal three types of chondrite-normalized patterns: N-group patterns are similar to cpx grains as they would form by fractionation from a range of mid ocean ridge basalts (MORB). They are typical for a few higher level dunitic samples as well as mafic cumulates. F-group patterns show light REE depletion, very strong middle REE fractionation and a positive Zr anomaly and occur in dunites only. R-group patterns are severely depleted in both light and heavy REEs relative to MORB-like cpx and two samples of the group display a positive Ti anomaly. They are also restricted to dunitic rocks. The patterns are explained in a two stage model in which an established dunite sequence, dominated by MORB-type cumulate signatures (N-group), was infiltrated by extremely refractory melts. During infiltration of the refractory melt chromatographic fractionation occurred, transforming N-group dunites into F-group and R-group dunites. The F-group patterns are composite patterns: heavy REE, Ti ± Zr reflect the original MORB-like cumulate dunite host, light REEs indicate equilibrium with the infiltrating, refractory melts. Steep slopes in the middle REEs reflect the position of the chromatographic front. For more intense percolation of refractory melts, R-group patterns with a positive Ti anomaly will form by the same process. The rest of the R-group patterns displaying no positive Ti anomaly may represent either the most intensely reacted host rocks or these dunites derive directly as cumulates from refractory melts. Only small volumes of refractory melt (a 5 m column) are required to imprint the observed trace element pattern on the thick original dunite sequence. One of several possible origins for the refractory melts is transformation of original MORB-type melts by way of chromatographic fractionation within the highly depleted, residual uppermost mantle. In the framework of an oceanic spreading centre, the migrating, refractory liquids are considered a late event following the main constructive stage dominated by aggregated melts. The study demonstrates that highly refractory melts can exist under oceanic spreading centres dominated by a MORB-like cumulate and volcanic sequence. Received: 2 September 1996 / Accepted: 20 November 1997     

Accelerated industrialization and employment opportunities in Malaysia

Malaysia is emerging as one of the most rapidly developing newly industrialized countries in the 1980s, mainly because it has pursued a strategy that is based on highly capital-intensive and export-oriented types of industries, financed by foreign capital and supported by a wide range of fiscal incentives. There has been, however, very little concern for the types and range of employment opportunities available. Based on unskilled labour, low wages and slow rates of employment absorption, this form of “industrialization-by-invitation” will in turn speed up processes or urbanization through rural-urban migration and create socio-economic problems of large city growth in the country.     

Partial fusion of basic granulites at 5 to 15 kbar: implications for the origin of TTG magmas

Partial fusion experiments with basic granulites (S6, S37) believed to represent the lower crust beneath the Eifel region (Germany) were performed at pressures from 5 to 15 kbar. Water-undersaturated experiments were carried out in the presence of 1 wt% H₂O plus 2.44 or 0.81 wt% CO₂ equivalent to mole fractions of H₂O/(H₂O + CO₂) of 0.5 and 0.75, respectively, of the volatile components added. At temperatures from 850 to 1100 °C the weight proportions of melt range from 7 to 30 %. Melt compositions change from trondhjemitic over tonalitic to dioritic with increasing degree of partial melting. Crystalline residua are plagioclase/pyroxene dominated at 5 kbar to garnet/pyroxene dominated at 15␣kbar. Dehydration melting was studied in granulite S35 similar in composition to S6. The magmatic precursors of the granulite xenoliths used in this study had geochemical characteristics of cumulate gabbro (metagabbro S37) and evolved melts (metabasalts S6, S35), respectively. Melts from granulite S37 match the major element compositions of natural trondhjemites and tonalites. At 5 kbar, their Al₂O₃ is relatively low, similar to tonalites from ophiolites. At 15 kbar, Al₂O₃ in the melts is high due to the near absence of plagioclase in the crystalline residua. The Al₂O₃ concentrations in 15 kbar melts from S6 (˜20 wt%) are higher than in natural tonalites. Depth constraints on the formation of tonalitic magmas in the continental crust are provided by REE (rare earth element) patterns of the synthetic melts calculated from the known REE abundances in metagabbro S37 and metabasalt S6 assuming batch melting and using partition coefficients from the literature. The REE patterns of tonalites from active continental margins and Archean trondhjemite-tonalite-granodiorite␣associations low in REE with La_N (chondrite normalised) from 10 to 30 and Yb_N from 1 to 2 are reproduced at pressures of 10 and 12.5 kbar from metagabbro S37 which displays a slightly L(light)REE enriched pattern with La_N = 8 and Yb_N = 3. Natural tonalites with La_N from 30 to 100 require a source richer in REE than granulite S37. At 15 kbar, H(heavy)REE_N in melts from granulite S37 are depressed below the level observed in natural tonalites due to the high proportion of garnet (>30 wt%) in the residue. Melts from metabasalt S6 (enriched in REE with La_N = 38 and Yb_N = 16) do not match the REE characteristics of natural tonalites under any conditions. Received: 1 July 1994 / Accepted: 11 September 1996     

Granulite facies lower crustal xenoliths from the Eifel,West Germany: petrological and geochemical aspects

Petrographic, petrological and geochemical data for 16 mafic meta-igneous, granulite facies lower crustal xenoliths from the East Eifel were collected in order to develop a model for the lower crustal history for this region. The xenoliths consist of plagioclase±amphibole±clinopyroxene±garnet±orthopyroxene±scapolite + opaque minerals±apatite±rutile±zircon. Garnet has reacted to a variable extent with plagioclase and clinopyroxene to form a corona of plagioclase_II+ amphibole + orthopyroxene_II. Pyroxenes and plagioclases show complex zoning patterns with regard to Al and Ca which can be interpreted in terms of P, T history. Decreasing temperature and pressure conditions are recorded by decreasing Al in clinopyroxene rims coexisting with increasing anorthite contents in plagioclase rims and the breakdown of garnet. In addition, a young heating event that affected the granulites to different degrees is inferred from the complementary Ca-zoning patterns in clino- and orthopyroxenes. Rare earth element (REE) patterns of whole rocks together with the trends displayed and fractionated liquids. REE analyses of the mineral separates display equilibrium partitioning patterns for amphibole and clinopyroxene, although isotopic data show that amphibole contains externally-derived Sr and Nd components not recognized in other minerals. At least a 4-stage history for the granulites is recorded: (1) intrusion and crystal fractionation of basaltic magmas in the lower crust, probably accompanied by crustal assimilation, (2) granulite facies metamorphism, (3) a decrease in temperature and pressure, and (4) a later heating event. The complicated thermal history is reflected in Sm–Nd mineral isochron ages which range from about 170 Ma down to about 100 Ma and cannot be assigned to distinct geological events. These ages correlate with inferred temperatures; the low ages are measured for xenoliths with the highest temperatures. In some cases the young heating event is likely to be responsible for partial resetting of the mineral isochrons.     

Chemical control of Al-solubility in orthopyroxene and its implications on pyroxene geothermometry

Two suites of spinel peridotites of the Westeifel/West Germany were found to have equilibrated in a narrow temperature interval each. Temperatures calculated from the CaO-solubility in orthopyroxene using experimental data of Lindsley and Dixon (1976) are 945° C to 980° C for the amphibole bearing Ia-suite and 1,150° C to 1,165° C for the Ib-suite. From the study of phase equilibria in both series it appears that Al-solubility in orthopyroxene is controlled by the composition of the coexisting spinel. Temperatures calculated from Al-solubility in orthopyroxene using an equation of Fujii (1976) derived from the univariant reaction en+spfo+Al-en in the MgO-Al₂O₃-SiO₂ system show a clear dependence on the FeCr₂O₄ component in the spinel phase, although ideal solution correction allowing for additional components was made. Temperatures obtained for the most chromite rich spinel — orthopyroxene pairs are 1,370° C and 1,240° C, respectively. These temperatures are by 220° C higher than those from Cr-poor pairs and those obtained from Ca solution in orthopyroxene.For practical purposes of geothermometry in spinel peridotites, an empirical equation allowing for the mole fraction of FeCr₂O₄ in spinel has been derived by a linear least squares fit to the orthopyroxene — spinel compositional data and temperatures calculated from the CaO-solubility of orthopyroxene in the present paper.     

Spinel peridotite xenoliths from the Tariat Depression, Mongolia. I: Major element chemistry and mineralogy of a primitive mantle xenolith suite

For mantle peridotite xenoliths from the Tariat Depression in central Mongolia an origin as partial melt residues has been inferred from the systematic change of bulk chemical compositions with mineral chemistries and modal compositions. The suite is dominated by primitive to slightly depleted lherzolites ranging from 15.7 to 7.9 wt.% of modal clinopyroxene, whereas harzburgites are rare. An increase of clinopyroxene to more than 20% in three samples is unrelated to liquid/crystal equilibria and is concluded to be the result of metamorphic differentiation. Leaving this enrichment of clinopyroxene aside, seven out of the twelve xenoliths studied come close to pyrolite in terms of mode and bulk chemistry. The primitive nature of these xenoliths is further emphazised by the low ratios of Cr/(Cr + Al + Fe) in their spinels, ranging from 0.075 to 0.087.

In the majority of the samples studied orthopyroxene is chemically zoned with Al and Cr decreasing from core to rim. Temperatures of about 1050°C and about 950°C are derived for cores and rims, respectively. No zoning is observed for Ca in orthopyroxene and temperatures obtained from the solubility of CaO in orthopyroxene are close to 950°C, which shows that with respect to Ca the orthopyroxenes had already reequilibrated to the lower temperature. This and the zoning of Al and Cr may be related to cooling after some initial thermal perturbation or to cooling in a diapir.     

Rhönit aus einem Melaphonolith vom Puy de Saint-Sandoux (Auvergne)

Zusammenfassung Mineralbestand, Chemismus und Erstarrungsbedingungen eines rhönitreichen melaphonolithischen Differentiates der Olivinnephelinitplatte des Puy de Saint-Sandoux (Auvergne) werden beschrieben. Von dem Rhönit aus dem Melaphonolith und einem weiteren aus dem Nephelindolerit vom Löbauer Berg (Sachsen) werden die Ergebnisse der chemischen Analysen sowie die optischen Konstanten mitgeteilt. Es wird versucht, im Verein mit in der Literatur enthaltenen Beobachtungen und experimentellen Untersuchungen, die Bildungsbedingungen des Rhönits abzuleiten.

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Rhoenite from a metaphonolite of Puy de Saint-Sandoux (Auvergne)

Summary Modal and chemical composition of a melaphonolithic differentiate in an olivine-nephelinite layer of the Puy de Saint-Sandoux (Auvergne) are given together with a discussion of the conditions of crystallization. The chemical composition and the optical data of the rhoenite in this rock and of another rhoenite from Löbauer Berg (Saxony) are presented. The conditions of rhoenite-formation are discussed on the basis of observations made in this and previous studies, as well as on experimental data.

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