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1.
ABSTRACT The Bouvet Triple Junction (BTJ) region in the South Atlantic, where the African, South American and Antarctica plates meet, is affected by several topographic/melting anomalies. Causes of these anomalies were investigated through a study of mantle-derived serpentinized peridotites sampled from three sites in the BTJ region: (1) the Inner Corner High at the intersection of the America Antarctic Ridge (AAR) with the Conrad transform; (2) the south wall of the Bouvet transform (South West Indian Ridge, SWIR); and (3) the eastern Bouvet SWIR Transform Intersection. The degree of melting undergone by these rocks was estimated from relic mineral major- and trace-element composition. Geochemical profiles from residual peridotites and associated basalts show a > 1000-km-wide melting anomaly centred on the Bouvet and Spiess topographic anomalies. 相似文献
2.
Trace element and isotope geochemistry of depleted peridotites from an N-MORB type ophiolite (Internal Liguride,N. Italy) 总被引:6,自引:0,他引:6
E. Rampone A. W. Hofmann G. B. Piccardo R. Vannucci P. Bottazzi L. Ottolini 《Contributions to Mineralogy and Petrology》1996,123(1):61-76
Mantle peridotites of the Internal Liguride (IL) units (Northern Apennines) constitute a rare example of the depleted lithosphere
of the Jurassic Ligurian Tethys. Detailed chemical (ICP-MS and SIMS techniques) and isotopic investigations on very fresh
samples have been performed with the major aim to constrain the timing and mechanism of their evolution and to furnish new
data for the geodynamic interpretation. The data are also useful to discuss some general geochemical aspects of oceanic-type
mantle. The studied samples consist of clinopyroxene-poor spinel lherzolites, showing incipient re-equilibration in the plagioclase-facies
stability field. The spinel-facies assemblage records high (asthenospheric) equilibration temperatures (1150–1250° C). Whole
rocks, and constituent clinopyroxenes, show a decoupling between severe depletion in highly incompatible elements [light rare
earth elements (LREE), Sr, Zr, Na, Ti] and less pronounced depletion in moderate incompatible elements (Ca, Al, Sc, V). Bulk
rocks also display a relatively strong M(middle)REE/H(heavy)REE fractionation. These compositional features indicate low-degree
(<10%) fractional melting, which presumably started in the garnet stability field, as the most suitable depletion mechanism.
In this respect, the IL ultramafics show strong similarity to abyssal peridotites. The Sr and Nd isotopic compositions, determined
on carefully handpicked clinopyroxene separates, indicate an extremely depleted signature (87Sr/86Sr=0.702203–0.702285; 143Nd/144Nd=0.513619–0.513775). The Sm/Nd model ages suggest that the IL peridotites melted most likely during Permian times. They
could record, therefore, the early upwelling and melting of mid ocean ridge basalt (MORB) type asthenosphere, in response
to the onset of extensional mechanisms which led to the opening of the Western Tethys. They subsequently cooled and experienced
a composite subsolidus evolution testified by multiple episodes of gabbroic intrusions and HT-LP retrograde metamorphic re-equilibration, prior to their emplacement on the sea floor. The trace element chemistry of IL peridotites
also provides useful information about the composition of oceanic-type mantle. The most important feature concerns the occurrence
of Sr and Zr negative anomalies (relative to “adjacent” REE) in both clinopyroxenes and bulk rocks. We suggest that such anomalies
reflect changes in the relative magnitude of Sr, Zr and REE partition coefficients, depending on the specific melting conditions.
Received: 15 February 1995/Accepted: 4 August 1995 相似文献
3.
A study of melt inclusions at Vulcano (Aeolian Islands, Italy): insights on the primitive magmas and on the volcanic feeding system 总被引:5,自引:0,他引:5
A. Gioncada R. Clocchiatti A. Sbrana P. Bottazzi D. Massare L. Ottolini 《Bulletin of Volcanology》1998,60(4):286-306
This work presents the results of a microthermometric and EPMA-SIMS study of melt inclusions in phenocrysts of rocks of the
shoshonitic eruptive complex of Vulcano (Aeolian Islands, Italy). Different primitive magmas related to two different evolutionary
series, an older one (50–25 ka) and a younger one (15 ka to 1890 A.D.), were identified as melt inclusions in olivine Fo88–91 crystals. Both are characterized by high Ca/Al ratio and present very similar Rb/Sr, B/Be and patterns of trace elements,
with Nb and Ti anomalies typical of a subduction zone. The two basalts present the same temperature of crystallization (1180±20 °C)
and similar volatile abundances. The H2O, S and Cl contents are relatively high, whereas magmatic CO2 concentrations are very low, probably due to CO2 loss before low-pressure crystallization and entrapment of melt inclusions. The mineral chemistry of the basaltic assemblages
and the high Ca/Al ratio of melt inclusions indicate an origin from a depleted, metasomatized clinopyroxene-rich peridotitic
mantle. The younger primitive melt is characterized with respect to the older one by higher K2O and incompatible element abundances, by lower Zr/Nb and La/Nb, and by higher Ba/Rb and LREE enrichment. A different degree
of partial melting of the same source can explain the chemical differences between the two magmas. However, some anomalies
in Sr, Rb and K contents suggest either a slightly different source for the two magmas or differing extents of crustal contamination.
Low-pressure degassing and cooling of the basaltic magmas produce shoshonitic liquids. The melt inclusions indicate evolutionary
paths via fractional crystallization, leading to trachytic compositions during the older activity and to rhyolitic compositions
during the recent one. The bulk-rock compositions record a more complex history than do the melt inclusions, due to the syneruptive
mixing processes commonly affecting the magmas erupted at Vulcano. The composition and temperature data on melt inclusions
suggest that in the older period of activity several shallow magmatic reservoirs existed; in the younger one a relatively
homogeneous feeding system is active. The shallow magmatic reservoir feeding the recent eruptive activity probably has a vertical
configuration, with basaltic magma in the deeper zones and differentiated magmas in shallower, low-volume, dike-like reservoirs.
Received: 11 March 1998 / Accepted: 14 July 1998 相似文献
4.
Vittorio Scribano Marco Viccaro Renato Cristofolini Luisa Ottolini 《Mineralogy and Petrology》2009,95(3-4):235-250
Three types of ultramafic xenoliths from the Hyblean area (Sicily) show prime evidence for mantle metasomatism, namely: 1) Spinel-facies depleted harzburgite veined by phlogopite-bearing clinopyroxenite; 2) Amphibole-bearing harzburgite; and 3) Al-spinel websterite. (2) and (3) exhibit glassy pockets having respectively mugearitic and basanitic compositions, but a little amount of glass with low Ca and very low alkalis in (2). Glasses generally show trace element distributions consistent with the partial melting of pargasite-dominated mineral assemblages. Abundant Ca-Mg-carbonate globules immersed in these glassy pockets testify to immiscibility between silicate and carbonatite melts. Silicate melts and hydrous-silicate supercritical fluids, which underwent phase separation during fluxing throughout the semi-brittle lithospheric mantle, may account for such metasomatizing processes. The nature and abundance of some fluid-mobile elements in glasses and hydrous minerals (especially the Ca-poor glass, with B?=?59 ppm, Li?=?27 ppm, Ba?=?700 ppm and phlogopite, with Ba?=?8,465 ppm, Sr?=?260 ppm, F?=?5,700 ppm) suggest that some hydrous fluids may derive from hydrothermally altered oceanic crust. Conversely, metasomatizing silicate melts probably have a deep-seated origin. These results confirm previous suggestions on the key role of mantle metasomatism in the origin of some alkaline Hyblean magmas. 相似文献
5.
P. Černý R. Chapman J. Staně M. Nová H. Baadsgaard M. Rieder M. Kavalová L. Ottolini 《Mineralogy and Petrology》1995,55(1-3):177-201
Summary The chemistry, structural parameters, polytypism, optical properties and Rb-Sr isotopes were examined in 11 to 60 samples of biotite, muscovite and lepidolite from the pegmatites at Roná (the type locality of lepidolite; 323 ± 4Ma) and Dobrá Voda (306 ± 9Ma) in western Moravia. At both localities, early endocontact biotite is followed inwards by muscovite and lepidolite, which is concentrated in and around the core. At Roná, a 1M lepidolite follows after 2M1 muscovite but all later generations of lepidolite are 2M2, close to Tri50 Ply50 and in part associated with muscovite 2M1. At Dobrá Voda, all lepidolite types are 1M and free of muscovite, and the late varieties approximate Tri30 Ply70. At both localities, a trend of increasing HF is indicated during the progress of mica crystallization, culminating in precipitation of topaz. Polytypism of lepidolite is not correlatable with any compositional or growth feature, or their combination. Throughout the mica crystallization, Rb/Cs decreases but K/Rb becomes reversed after an initial decrease. Boron is partitioned preferentially into muscovite (up to 1.10 wt.% B2O3) but Be, Zn, Mn and Sc are enhanced in lepidolite. A slight increase in Fe, Ba and Cl in the last generation of lepidolite might be possibly due to mixing of residual pegmatite fluids with metamorphic pore solutions.
With 9 Figures 相似文献
Geochemische und strukturelle Entwicklung der Glimmer in den Pegmatiten von Roná und Dobrá Voda, Tschechische Republik
Zusammenfassung In 11 bis 60 Proben von Biotit, Muskovit und Lepidolith aus den Pegmatiten von Roná (Typlokalität des Lepidoliths; 323 ± 9 Ma) in Westmähren wurden Chemie, Struktur-parameter, Polytypie, optische Eigenschaften und Rb-Sr-Isotopie untersucht. An beiden Lokalitäten wird früher Biotit an Endokontakten nach Innen von Muskovit und Lepidolith gefolgt, letzterer ist in und um den Kern konzentriert. In Roná folgt 1M-Lepidolith auf 2M1-Muskovit, aber alle späteren Lepidolithgenerationen sind 2M2, nahe Tri50Ply50 und zum Teil mit 2M1-Muskovit vergesellschaftet. In Dobrá Voda sind alle Lepidolithe vom Typ 1M und frei von Muskovit, die späten Varietäten kommen Tri50Ply50 nahe. An beiden Lokalitäten ist während des Fortschreitens der Glimmerkristallisation eine Tendenz von steigendem HF angezeigt, die in der Ausfällung von Topas ihren Höhepunkt findet. Die Polytypie des Lepidoliths kann nicht mit irgendeiner Eigenheit der Zusammensetzung oder des Wachstums korreliert worden, auch nicht mit einer Kombination von diesen. Während der ganzen Glimmerkristallisation nimmt Rb/Cs ab, aber die Tendenz von K/Rb ändert sich nach anfänglichem Abfall. Das Bor verteilt sich bevorzugt auf den Muskovit (bis zu 1.10 Gew. -% B2O3), aber die Be-, Zn-, Mn- und Sc-Gehalte sind im Lepidolith erhöht. Ein leichter Ansteig von Fe, Ba und Cl in der letzten Lepidolithgeneration könnte vielleicht durch eine Mischung von pegmatitischen Restlösungen mit metamorphen Porenlösungen verursacht sein.
With 9 Figures 相似文献
6.
7.
Fernando Scordari Emanuela Schingaro Gennaro Ventruti Maria Lacalamita Luisa Ottolini 《Physics and Chemistry of Minerals》2008,35(3):163-174
The crystal chemistry of red phlogopites from Mt. Vulture (Italy) ignimbrites has been studied by electron microprobe, secondary
ion mass spectrometry (SIMS), single crystal structural investigation and Fourier transform infrared (FTIR) spectroscopy.
The analysed phlogopite has Fe/(Fe + Mg) ∼ 0.35, TiO2 (wt%): 2.8–5.0 and H2O (wt%): 1.24–3.37. Infrared spectra revealed the presence of bands due to the NH4+ and H2O stretching and bending vibrations. The samples belong to the 1M polytype. The bimodal behaviour of several structural parameters allows red micas to be clustered into two distinct groups:
K+ ↔ NH4+, H2O and M3+-vacancy substitutions dominate in the first group; M3+,4+-oxy, in the second group. It has to be pointed out that quantitative analysis of hydrogen (via SIMS) together with the characterization
of the local environment of the anionic site (via FTIR) are fundamental in assessing the correct structural formula and the
substitution mechanisms in micas.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
8.
Rivalenti Giorgio Mazzucchelli Maurizio Vannucci Riccardo Hofmann Albrecht W. Ottolini Luisa Bottazzi Piero Obermiller Walter 《Contributions to Mineralogy and Petrology》1995,122(3):275-288
Field, mineralogical and petrological data are presented on a newly found carbonatite occurrence associated with “kamafugite”
lava at Cupaello, central Italy. This carbonatite occurrence is part of the Late Pleistocene Umbria-Latium ultra-alkaline
district (ULUD) which extends southwards within the Apennines to Mount Vulture, delineating an important magmatic province
along the most peripheral belt of the Tyrrhenian extensional tectonic system. This province is distinct, but probably related
genetically with the more abundant and common leucite-bearing assemblages of the Roman Comagmatic Region and represents the
first reported occurrence of carbonatite assemblages in the Mediterranean Basin. The Cupaello suite indicates that primary
or near-primary mantle silicate melts of “kamafugitic” composition are transitional with Ca-carbonatite liquid and provides
direct evidence of immiscibility of carbonatite from “kamafugite” magma. It is inferred that a primary mantle origin of Ca-carbonatites
is conditional upon a potential silicate magma that may be coupled with the carbonatite, but may not have reached the surface.
The data indicate a strong genetic link between ULUD Ca-carbonatites and some African analogues, supporting the view that
their genesis depends on similar source and associated tectonic conditions.
Received: 17 January 1995 / Accepted: 14 June 1995 相似文献
9.
E. Rampone G. B. Piccardo R. Vannucci P. Bottazzi L. Ottolini 《Contributions to Mineralogy and Petrology》1993,115(1):1-17
Mantle peridotites of the External Liguride (EL) Units (Northern Apennines) mainly consist of fertile spinel-lherzolites partially recrystallized to plagioclase-facies assemblages, and are consequently appropriate to investigate the interphase element partitioning related to the transition from spinel- to plagioclase-facies stability field. Evidence for the development of the plagioclase-facies assemblage is mainly given by: (1) large exsolution lamellae of orthopyroxene and plagioclase within spinel-facies clinopyroxene; (2) plagioclase rims around spinel; (3) granoblastic domains made up of olivine+plagioclase±clino-and orthopyroxene. In situ major and trace [REE (rare-earth elements), Ti, Sc, V, Cr, Sr, Y, Zr and Ba] element mineral analyses have been performed, by electron and ion probe, on selected samples which show the progressive development of the plagioclase-bearing assemblage. The main compositional variations observed during the change from spinel- to plagioclase-facies minerals are as follows: (1) clinopyroxenes decrease in Al, Na, Sr, Eu/Eu* and increase in Y, V, Sc, Cr, Zr and Ti; (2) amphiboles decrease in Eu/Eu*, Sr, Ba and increase in Zr and V; (3) spinels decrease in Al and increase in Cr and Ti. The most striking feature is the decoupling in the behaviour of similarly incompatible elements (D about 0.1) in clinopyroxene, e.g. Sr decrease is mirrored by Zr increase. Massbalance calculations indicate that the trace element interphase redistribution documented in the EL peridotites occurred in a closed system and in response to the metamorphic reaction governing the transition from the spinel- to the plagioclase-facies stability field. The observed element partitioning reveals, moreover, that subsolidus re-equilibration processes in the upper mantle produce HFSE (high-field-strength element)/REE fractionation in minerals, which must be evaluated for a reliable determination of mineral-melt distribution coefficients. The results of this study furnish evidence for subsolidus metamorphic evolution during decompression, without concomitant partial melting processes. This is consistent with the interpretation that the EL peridotites represent subcontinental lithospheric mantle emplaced at the surface in response to lithospheric thinning and tectonic denudation mechanisms related to the Triassic-Jurassic rifting of the Ligure-Piedmontese basin. 相似文献
10.
The effect of halogens on Zr diffusion and zircon dissolution in hydrous metaluminous granitic melts 总被引:1,自引:0,他引:1
Don R. Baker Aida Conte Carmela Freda Luisa Ottolini 《Contributions to Mineralogy and Petrology》2002,142(6):666-678
Diffusion of Zr and zircon solubility in hydrous, containing approximately 4.5 wt% H2O, metaluminous granitic melts with halogens, either 0.35 wt% Cl (LCl) or 1.2 wt% F (MRF), and in a halogen-free melt (LCO) were measured at 1.0 GPa and temperatures between 1,050 and 1,400 °C in a piston-cylinder apparatus using the zircon dissolution technique. Arrhenius equations for Zr diffusion in each hydrous melt composition are, for LCO with 4.4ǂ.4 wt% H2O: % MathType!MTEF!2!1!+- % feaaeaart1ev0aaatCvAUfKttLearuavP1wzZbItLDhis9wBH5garm % Wu51MyVXgaruWqVvNCPvMCG4uz3bqee0evGueE0jxyaibaieYlf9ir % Veeu0dXdh9vqqj-hEeeu0xXdbba9ev6pc9fs0-rqaqpepmKs4qpepe % I8kaL8kuc9pgc9q8qqaq-dhH6hb9hs0dXdHu6deP0u0-vr0-vr0db8 % meaabaqaciGacaGaaeaabaWaaeaaeaaakeaacqWGebarcqGH9aqpcq % aIYaGmcqGGUaGlcqaI4aaocqaI4aaocqGHXcqScqaIWaamcqGGUaGl % cqaIWaamcqaIZaWmcqWG4baEcqaIXaqmcqaIWaamdaahaaWcbeqaai % abgkHiTiabiIda4aaakiGbcwgaLjabcIha4jabcchaWnaabmaabaWa % aSaaaeaacqGHsislcqaIXaqmcqaI0aancqaIWaamcqGGUaGlcqaIXa % qmcqGHXcqScqaIZaWmcqaIZaWmcqGGUaGlcqaI5aqoaeaacqWGsbGu % cqWGubavaaaacaGLOaGaayzkaaaaaa!571F! D = 2.88 ±0.03x10 - 8 exp( [( - 140.1 ±33.9)/(RT)] )D = 2.88 \pm 0.03x10^{ - 8} \exp \left( {{{ - 140.1 \pm 33.9} \over {RT}}} \right) , for LCl with 4.5ǂ.5 wt% H2O: % MathType!MTEF!2!1!+- % feaaeaart1ev0aaatCvAUfKttLearuavP1wzZbItLDhis9wBH5garm % Wu51MyVXgaruWqVvNCPvMCG4uz3bqee0evGueE0jxyaibaieYlf9ir % Veeu0dXdh9vqqj-hEeeu0xXdbba9ev6pc9fs0-rqaqpepmKs4qpepe % I8kaL8kuc9pgc9q8qqaq-dhH6hb9hs0dXdHu6deP0u0-vr0-vr0db8 % meaabaqaciGacaGaaeaabaWaaeaaeaaakeaacqWGebarcqGH9aqpcq % aIYaGmcqGGUaGlcqaIZaWmcqaIZaWmcqGHXcqScqaIWaamcqGGUaGl % cqaIWaamcqaI1aqncqWG4baEcqaIXaqmcqaIWaamdaahaaWcbeqaai % abgkHiTiabisda0aaakiGbcwgaLjabcIha4jabcchaWnaabmaabaWa % aSaaaeaacqGHsislcqaIYaGmcqaI1aqncqaI0aancqGGUaGlcqaI4a % aocqGHXcqScqaI2aGncqaI0aancqGGUaGlcqaIXaqmaeaacqWGsbGu % cqWGubavaaaacaGLOaGaayzkaaaaaa!5719! D = 2.33 ±0.05x10 - 4 exp( [( - 254.8 ±64.1)/(RT)] )D = 2.33 \pm 0.05x10^{ - 4} \exp \left( {{{ - 254.8 \pm 64.1} \over {RT}}} \right) and for MRF with 4.9ǂ.3 wt% H2O: % MathType!MTEF!2!1!+- % feaaeaart1ev0aaatCvAUfKttLearuavP1wzZbItLDhis9wBH5garm % Wu51MyVXgaruWqVvNCPvMCG4uz3bqee0evGueE0jxyaibaieYlf9ir % Veeu0dXdh9vqqj-hEeeu0xXdbba9ev6pc9fs0-rqaqpepmKs4qpepe % I8kaL8kuc9pgc9q8qqaq-dhH6hb9hs0dXdHu6deP0u0-vr0-vr0db8 % meaabaqaciGacaGaaeaabaWaaeaaeaaakeaacqWGebarcqGH9aqpcq % aIYaGmcqGGUaGlcqaI1aqncqaI0aancqGHXcqScqaIWaamcqGGUaGl % cqaIWaamcqaIZaWmcqWG4baEcqaIXaqmcqaIWaamdaahaaWcbeqaai % abgkHiTiabiwda1aaakiGbcwgaLjabcIha4jabcchaWnaabmaabaWa % aSaaaeaacqGHsislcqaIYaGmcqaIYaGmcqaIZaWmcqGGUaGlcqaI4a % aocqGHXcqScqaIXaqmcqaI1aqncqGGUaGlcqaI1aqnaeaacqWGsbGu % cqWGubavaaaacaGLOaGaayzkaaaaaa!5715! D = 2.54 ±0.03x10 - 5 exp( [( - 223.8 ±15.5)/(RT)] )D = 2.54 \pm 0.03x10^{ - 5} \exp \left( {{{ - 223.8 \pm 15.5} \over {RT}}} \right) . Solubilities determined by the dissolution technique were reversed for LCO +4.5ǂ.5 wt% H2O by crystallization of a Zr-enriched glass of LCO composition at 1,200 and 1,050 °C at 1.0 GPa. The solubility data were used to calculate partition coefficients of Zr between zircon and hydrous melt, which are given by the following expressions: for LCO % MathType!MTEF!2!1!+- % feaaeaart1ev0aaatCvAUfKttLearuavP1wzZbItLDhis9wBH5garm % Wu51MyVXgaruWqVvNCPvMCG4uz3bqee0evGueE0jxyaibaieYlf9ir % Veeu0dXdh9vqqj-hEeeu0xXdbba9ev6pc9fs0-rqaqpepmKs4qpepe % I8kaL8kuc9pgc9q8qqaq-dhH6hb9hs0dXdHu6deP0u0-vr0-vr0db8 % meaabaqaciGacaGaaeaabaWaaeaaeaaakeaacyGGSbaBcqGGUbGBcq % WGebardaqhaaWcbaGaemOwaOLaemOCaihabaGaemOEaONaemyAaKMa % emOCaiNaem4yamMaem4Ba8MaemOBa4Maei4la8IaemyBa0Maemyzau % MaemiBaWMaemiDaqhaaOGaeyypa0JaeGymaeJaeiOla4IaeGOnayJa % eG4mamZaaeWaaeaadaWcaaqaaiabigdaXiabicdaWiabicdaWiabic % daWiabicdaWaqaaiabdsfaubaaaiaawIcacaGLPaaacqGHsislcqaI % 1aqncqGGUaGlcqaI4aaocqaI3aWnaaa!5924! lnDZrzircon/melt = 1.63( [10000/(T)] ) - 5.87\ln D_{Zr}^{zircon/melt} = 1.63\left( {{{10000} \over T}} \right) - 5.87 , for LCl % MathType!MTEF!2!1!+- % feaaeaart1ev0aaatCvAUfKttLearuavP1wzZbItLDhis9wBH5garm % Wu51MyVXgaruWqVvNCPvMCG4uz3bqee0evGueE0jxyaibaieYlf9ir % Veeu0dXdh9vqqj-hEeeu0xXdbba9ev6pc9fs0-rqaqpepmKs4qpepe % I8kaL8kuc9pgc9q8qqaq-dhH6hb9hs0dXdHu6deP0u0-vr0-vr0db8 % meaabaqaciGacaGaaeaabaWaaeaaeaaakeaacyGGSbaBcqGGUbGBcq % WGebardaqhaaWcbaGaemOwaOLaemOCaihabaGaemOEaONaemyAaKMa % emOCaiNaem4yamMaem4Ba8MaemOBa4Maei4la8IaemyBa0Maemyzau % MaemiBaWMaemiDaqhaaOGaeyypa0JaeGymaeJaeiOla4IaeGinaqJa % eG4naCZaaeWaaeaadaWcaaqaaiabigdaXiabicdaWiabicdaWiabic % daWiabicdaWaqaaiabdsfaubaaaiaawIcacaGLPaaacqGHsislcqaI % 0aancqGGUaGlcqaI3aWncqaI1aqnaaa!5920! lnDZrzircon/melt = 1.47( [10000/(T)] ) - 4.75\ln D_{Zr}^{zircon/melt} = 1.47\left( {{{10000} \over T}} \right) - 4.75 and, for MRF by % MathType!MTEF!2!1!+- % feaaeaart1ev0aaatCvAUfKttLearuavP1wzZbItLDhis9wBH5garm % Wu51MyVXgaruWqVvNCPvMCG4uz3bqee0evGueE0jxyaibaieYlf9ir % Veeu0dXdh9vqqj-hEeeu0xXdbba9ev6pc9fs0-rqaqpepmKs4qpepe % I8kaL8kuc9pgc9q8qqaq-dhH6hb9hs0dXdHu6deP0u0-vr0-vr0db8 % meaabaqaciGacaGaaeaabaWaaeaaeaaakeaacyGGSbaBcqGGUbGBcq % WGebardaqhaaWcbaGaemOwaOLaemOCaihabaGaemOEaONaemyAaKMa % emOCaiNaem4yamMaem4Ba8MaemOBa4Maei4la8IaemyBa0Maemyzau % MaemiBaWMaemiDaqhaaOGaeyypa0JaeGymaeJaeiOla4IaeGinaqJa % eG4naCZaaeWaaeaadaWcaaqaaiabigdaXiabicdaWiabicdaWiabic % daWiabicdaWaqaaiabdsfaubaaaiaawIcacaGLPaaacqGHsislcqaI % 0aancqGGUaGlcqaI5aqocqaIXaqmaaa!591C! lnDZrzircon/melt = 1.47( [10000/(T)] ) - 4.91\ln D_{Zr}^{zircon/melt} = 1.47\left( {{{10000} \over T}} \right) - 4.91 . Experiments on the same compositions, but with water contents down to 0.5 wt%, demonstrated reductions in both the diffusion coefficient of Zr and zircon solubility in the melt. The addition of halogens at the concentration levels studied to metaluminous melts has a small effect on either the diffusion of Zr in the melt, or the solubility of zircon at all water concentrations and temperatures investigated. At 800 °C, the calculated diffusion coefficient of Zr is lowest in LCl, 9᎒-17 m2 s-1, and is highest in LCO, 4᎒-15 m2 s-1. Extrapolation of the halogen-free solubility data to a magmatic temperature of 800 °C yields solubilities of approximately one-third of those directly measured in similar compositions, predicted by earlier studies of zircon dissolution and based upon analyses of natural rocks. This discrepancy is attributed to the higher oxygen fugacity of the experiments of this study compared with previous studies and nature, and the effect of oxygen fugacity on the structural role of iron in the melt, which, in turn, affects zircon solubility, but does not significantly affect Zr diffusion. 相似文献