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1.
We have investigated the loss of H2O from olivine-hosted melt inclusions (MIs) by designing an experiment using tephra samples that cooled at different rates owing to their different sizes: ash, lapilli, and bomb samples that were deposited on the same day (10/17/74) of the sub-Plinian eruption of Volcán de Fuego in Guatemala. Ion microprobe, laser ablation-ICPMS, and electron probe analyses show that MIs from ash and lapilli record the highest H2O contents, up to 4.4 wt%. On the other hand, MIs from bombs indicate up to 30 % lower H2O contents (loss of ~1 wt% H2O) and 10 % post-entrapment crystallization of olivine. This evidence is consistent with the longer cooling time available for a bomb-sized clast, up to 10 min for a 3–4-cm radius bomb, assuming conductive cooling and the fastest H diffusivities measured in olivine (D~10?9 to 10?10 m2/s). On the other hand, several lines of evidence point to some water loss prior to eruption, during magma ascent and degassing in the conduit. Thus, results point to both slower post-eruptive cooling and slower magma ascent affecting MIs from bombs, leading to H2O loss over the timescale of minutes to hours. The important implication of this study is that a significant portion of the published data on H2O concentrations in olivine-hosted MIs may reflect unrecognized H2O loss via diffusion. This work highlights the importance of reporting clast and MI sizes in order to assess diffusive effects and the potential benefit of using water loss as a chronometer of magma ascent.  相似文献   

2.
Melt inclusions in olivine Fo83–72 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.  相似文献   

3.
In volatile-saturated magmas, degassing and crystallisation are interrelated processes which influence the eruption style. Melt inclusions provide critical information on volatile and melt evolution, but this information can be compromised significantly by post-entrapment modification of the inclusions. We assess the reliability and significance of pyroxene-hosted melt inclusion analyses to document the volatile contents (particularly H2O) and evolution of intermediate arc magmas at Volcán de Colima, Mexico. The melt inclusions have maximal H2O contents (≤4 wt%) consistent with petrological estimates and the constraint that the magmas crystallised outside the amphibole stability field, demonstrating that pyroxene-hosted melt inclusions can preserve H2O contents close to their entrapment values even in effusive eruptions with low effusion rates (0.6 m3 s?1). The absence of noticeable H2O loss in some of the inclusions requires post-entrapment diffusion coefficients (≤1 × 10?13 m2 s?1) at least several order of magnitude smaller than experimentally determined H+ diffusion coefficient in pyroxenes. The H2O content distribution is, however, not uniform, and several peaks in the data, interpreted to result from diffusive H2O reequilibration, are observed around 1 and 0.2 wt%. H2O diffusive loss is also consistent with the manifest lack of correlations between H2O and CO2 or S contents. The absence of textural evidence supporting post-entrapment H2O loss suggests that diffusion most likely occurred via melt channels prior to sealing of the inclusions, rather than through the host crystals. Good correlation between the melt inclusion sealing and volcano-tectonic seismic swarm depths further indicate that, taken as a whole, the melt inclusion population accurately records the pre-eruptive conditions of the magmatic system. Our data demonstrate that H2O diffusive loss is a second-order process and that pyroxene-hosted melt inclusions can effectively record the volatile contents and decompression-induced crystallisation paths of vapour-saturated magmas.  相似文献   

4.
The mobility of H2O and D2O by diffusion through quartz is illustrated with H2O-rich fluid inclusions synthesized at 600 °C and 337 MPa, within the α-quartz stability field. Inclusions are re-equilibrated at the same experimental conditions within a pure D2O fluid environment. Consequently, a gradient in volatile fugacities is the only driving force for diffusion, in the absence of pressure gradients and deformation processes. Up to 100 individual inclusions are analyzed in each experiment before and after re-equilibration by microscopic investigation, microthermometry, and Raman spectroscopy. Changes in fluid inclusion composition are obtained from the ice-melting temperatures, and density changes are obtained from total homogenization temperatures. After 1-day re-equilibration, inclusions already contain up to 11 mol % D2O. A maximum concentration of 63 mol % D2O is obtained after 40-day re-equilibration. D2O concentration profiles in quartz are determined from the concentration in inclusions as a function of their distance to the quartz surface. These profiles illustrate that deep inclusions contain less D2O than shallow inclusions. At equal depths, a variety of D2O concentration is observed as a function of fluid inclusion size: Small inclusions are stronger effected compared with large inclusions. A series of 19-day re-equilibration experiments are performed at 300, 400, 500, and 600 °C (at 337 MPa), at the same conditions as the original synthesis. The threshold temperature of diffusion is estimated around 450 °C at 337 MPa, because D2O is not detected in inclusions from re-equilibration experiments at 300 and 400 °C, whereas maximally 26 mol % D2O is detected at 500 °C. Our study indicates that the isotopic composition of natural fluid inclusions may be easily modified by re-equilibration processes, according to the experimental conditions at 600 °C and 337 MPa.  相似文献   

5.
Melt inclusions were investigated in olivine phenocrysts from the New Caledonia boninites depleted in CaO and TiO2 and enriched in SiO2 and MgO. The rocks are composed of olivine and pyroxene phenocrysts in a glassy groundmass. The olivine phenocrysts contain melt inclusions consisting of glass, a fluid vesicle, and daughter olivine and orthopyroxene crystals. The daughter minerals are completely resorbed in the melt at 1200?C1300°C, whereas the complete dissolution of the fluid phase was not attained in our heating experiments. The compositions of reheated and naturally quenched melt inclusions, as well as groundmass glasses were determined by electron microprobe analysis and secondary ion mass spectrometry. Partly homogenized melts (with gas) contain 12?C16 wt % MgO. The glasses of inclusions and groundmass are significantly different in H2O content: up to 2 wt % in the glasses of reheated inclusions, up to 4 wt % in naturally quenched inclusions, and 6?C8 wt % in groundmass glasses. A detailed investigation revealed a peculiar zoning in olivine: its Mg/(Mg + Fe) ratio increased in a zone directly adjacent to the glass of inclusions. This effect is probably related to partial water (hydrogen) loss and Fe oxidation after inclusion entrapment. The numerical modeling of such a process showed that the water loss was no higher than a few tenths of percent and could not be responsible for the considerable difference between the compositions of inclusions and groundmass glasses. It is suggested that the latter were enriched in H2O after the complete solidification of the rock owing to interaction with seawater. Based on the obtained data, the compositions of primary boninite magmas were estimated, and it was supposed that variations in melt composition were related not only to olivine and pyroxene fractionation from a single primary melt but also to different degrees and (or) depths of magma derivation.  相似文献   

6.
The products of the 1974 eruption of Fuego, a subduction zone volcano in Guatemala, have been investigated through study of silicate melt inclusions in olivine. The melt inclusions sampled liquids in regions where olivine, plagioclase, magnetite, and augite were precipitating. Comparisons of the erupted ash, groundmass, and melt inclusion compositions suggest that the inclusions represent samples of liquids present in a thermal boundary layer of the magma body. The concentrations of H2O and CO2 in glass inclusions were determined by a vacuum fusion manometric technique using individual olivine crystals (Fo77 to Fo71) with glass inclusion compositions that ranged from high-alumina basalt to basaltic andesite. Water, Cl, and K2O concentrations increased by a factor of two as the olivine crystals became more iron-rich (Fo77 to Fo71) and as the glass inclusions increased in SiO2 from 51 to 54 wt.% SiO2. The concentration of H2O in the melt increased from 1.6 wt.% in the least differentiated liquid to about 3.5% in a more differentiated liquid. Carbon dioxide is about an order of magnitude less abundant than H2O in these inclusions. The gas saturation pressures for pure H2O in equilibrium with the melt inclusions, which were calculated from the glass inclusion compositions using the solubility model of Burnham (1979), are given approximately by P(H2O)(Pa)=(SiO2−48.5 wt.%) × 1.45 × 107. The concentrations of water in the melt and the gas saturation pressures increased from about 1.5% to 3.5% and from 300 to 850 bars, respectively, during pre-eruption crystallization.  相似文献   

7.
We describe and model a potential re-equilibration process that can affect compositions of melt inclusions in magnesian olivine phenocrysts. This process, referred to as “Fe-loss”, can operate during natural pre-eruptive cooling of host magma and results in lower FeOt and higher MgO contents within the initially trapped volume of inclusion. The extent of Fe-loss is enhanced by large temperature intervals of magma cooling before eruption. The compositions of homogenised melt inclusions in olivine phenocrysts from several subduction-related suites demonstrate that (1) Fe-loss is a common process, (2) the maximum observed degree of re-equilibration varies between suites, and (3) within a single sample, variable degrees of re-equilibration can be recorded by melt inclusions trapped in olivine phenocrysts of identical composition. Our modelling also demonstrates that the re-equilibration process is fast going to completion, in the largest inclusions in the most magnesian phenocrysts it is completed within 2 years. The results we obtained indicate that the possibility of Fe-loss must be considered when estimating compositions of parental subduction-related magmas from naturally quenched glassy melt inclusions in magnesian olivine phenocrysts. Compositions calculated from glassy inclusions affected by Fe-loss will inherit not only erroneously low FeOt contents, but also low MgO due to the inherited higher Mg##of the residual melt in re-equilibrated inclusions. We also demonstrate that due to the higher MgO contents of homogenised melt inclusions affected by Fe-loss, homogenisation temperatures achieved in heating experiments will be higher than original trapping temperatures. The extent of overheating will increase depending on the degree of re-equilibration, and can reach up to 50 °C in cases where complete re-equilibration occurs over a cooling interval of 200 °C. Received: 2 November 1998 / Accepted: 27 September 1999  相似文献   

8.
The chemical compositions of melt inclusions in a primitive and an evolved basalt recovered from the mid-Atlantic ridge south of the Kane Fracture Zone (23°–24°N) are determined. The melt inclusions are primitive in composition (0.633–0.747 molar Mg/(Mg+Fe2+), 1.01–0.68 wt% TiO2) and are comparable to other proposed parental magmas except in having higher Al2O3 and lower CaO. The primitive melt inclusion compositions indicate that the most primitive magmas erupted in this region are not near primary magma compositions. Olivine and plagioclase microphenocrysts are close to exchange equilibrium with their respective basalt glasses, whose compositions are displaced toward olivine from 1 atm three phase saturation. The most primitive melt inclusion compositions are close to exchange equilibrium with the anorthitic cores of zoned plagioclases (An78.3-An83.1; the hosts for the melt inclusions in plagioclase) and with olivines more forsteritic (Fo89-Fo91) than the olivine microphenocrysts (the hosts for the melt inclusions in olivine). Xenocrystic olivine analyzed is Fo89 but contains no melt inclusions. These observations indicate that olivines have exchanged components with the melt after melt inclusion entrapment, whereas plagioclase compositions have remained the same since melt inclusion entrapment. Common denominator element ratio diagrams and oxide versus oxide variation diagrams show that the melt inclusion compositions, which represent liquids higher along the liquid line of descent, are related to the glass compositions by the fractionation of olivine, plagioclase and clinopyroxene (absent from the mincral assemblage), probably occurring at elevated pressures. A model is proposed whereby clinopyroxene segregates from the melt at elevated pressures (to account for its absence in the erupted lavas that have the chemical imprint of clinopyroxene fractionation). Zoned plagioclases in the erupted lavas are thought to be survivors of decompressional melting during magma ascent. Since similar primitive melt inclusions occur in olivine microphenocrysts and in the cores of zoned plagioclases, any model must account for all phases present.  相似文献   

9.
The compositions of approximately 70 naturally quenched melt inclusions in olivine, clinopyroxene, orthopyroxene, and plagioclase phenocrysts from tephra of the soil–pyroclastic cover of Simushir Island (Central Kuril Islands) were studied. The concentrations of the major rock-forming components, H2O, S, and Cl were analyzed in inclusions. The reconstructed melts contain 48.6–78.4 wt % SiO2, 0.3–8.26 wt % MgO, and 0.12–1.72 wt % K2O. The concentration of S and Cl in the melts changes regularly with increasing SiO2 content: from 0.14 to ~0.02 wt % S and from ~0.05 to ~0.28 wt % Cl. The content of H2O in parental melts is 4.2–4.5 wt %.  相似文献   

10.
The results of a complex study of melt inclusions in olivine phenocrysts contained in unaltered kimberlites from the Udachnaya-East pipe indicate that the inclusions were captured late during the magmatic stage, perhaps, under a pressure of <1 kbar and a temperature of ≤800°C. The inclusions consist of fine crystalline aggregates (carbonates + sulfates + chlorides) + gas ± crystalline phases. Minerals identified among the transparent daughter phases of the inclusions are silicates (tetraferriphlogopite, olivine, humite or clinohumite, diopside, and monticellite), carbonates (calcite, dolomite, siderite, northupite, and Na-Ca carbonates), Na and K chlorides, and alkali sulfates. The ore phases are magnetite, djerfisherite, and monosulfide solid solution. The inclusions are derivatives of the kimberlite melt. The complex silicate-carbonate-salt composition of the secondary melt inclusions in olivine from the kimberlite suggests that the composition of the kimberlite melt near the surface differed from that of the initial melt composition in having higher contents of CaO, FeO, alkalis, and volatiles (CO2, H2O, F, Cl, and S) at lower concentrations of SiO2, MgO, Al2O3, Cr2O3, and TiO2. Hence, when crystallizing, the kimberlite melt evolved toward carbonatite compositions. The last derivatives of the kimberlite melt had an alkaline carbonatite composition.  相似文献   

11.
As the water concentration in magma decreases during magma ascent, olivine-hosted melt inclusions will reequilibrate with the host magma through hydrogen diffusion in olivine. Previous models showed that for a single spherical melt inclusion in the center of a spherical olivine, the rate of diffusive reequilibration depends on the partition coefficient and diffusivity of hydrogen in olivine, the radius of the melt inclusion, and the radius of the olivine. This process occurs within a few hours and must be considered when interpreting water concentration in olivine-hosted melt inclusions. A correlation is expected between water concentration and melt inclusion radius, because small melt inclusions are more rapidly reequilibrated than large ones when the other conditions are the same. This study investigates the effect of diffusive water loss in natural samples by exploring such a correlation between water concentration and melt inclusion radius, and shows that the correlation can be used to infer the initial water concentration and magma ascent rate. Raman and Fourier transform infrared spectroscopy measurements show that 31 melt inclusions (3.6–63.9 μm in radius) in six olivines from la Sommata, Vulcano Island, Aeolian Islands, have 0.93–5.28 wt% water, and the host glass has 0.17 wt% water. The water concentration in the melt inclusions shows larger variation than the data in previous studies (1.8–4.52 wt%). It correlates positively with the melt inclusion radius, but does not correlate with the major element concentrations in the melt inclusions, which is consistent with the hypothesis that the water concentration has been affected by diffusive water loss. In a simplified hypothetical scenario of magma ascent, the initial water concentration and magma ascent rate are inferred by numerical modeling of the diffusive water loss process. The melt inclusions in each olivine are assumed to have the same initial water concentration and magma ascent rate. The melt inclusions are assumed to be quenched after eruption (i.e., the diffusive water loss after eruption is not considered). The model results show that the melt inclusions initially had 3.9–5.9 wt% water and ascended at 0.002–0.021 MPa/s before eruption. The overall range of ascent rate is close to the lower limit of previous estimates on the ascent rate of basalts.  相似文献   

12.
Geochemical data from melt inclusions in olivine phenocrysts in a picritic basalt from the Siqueiros Transform Fault on the northern East Pacific Rise provide insights into the petrogenesis of mid-ocean ridge basalts (MORB). The fresh lava contains ~10% of olivine phenocrysts (Fo89.3-91.2) and rare, small (<1 mm) plagioclase phenocrysts with subhedral to irregular shapes with a range of compositions (An80-90, An57-63). Melt inclusions in olivine phenocrysts are glassy, generally rounded in shape and vary in size from a few to ~200 µm. Although most of the inclusions have compositions that are generally consistent with being representative of parental melts for the pillow-rim glasses, several inclusions are clearly different. One inclusion, which contains a euhedral grain of high-Al, low-Ti spinel, has a composition unlike any melt inclusions previously described from primitive phenocrysts in MORB. It has a very high Al2O3 (~20 wt%), very low TiO2 (~0.04 wt%) and Na2O (~1 wt%) contents, and a very high CaO/Na2O value (~14). The glass inclusion is strongly depleted in all incompatible elements (La =0.052 ppm; Yb =0.34; La/Sm(n) ~0.27), but it has large positive Sr and Eu anomalies (Sr/Sr* ~30; Eu/Eu* ~3) and a negative Zr anomaly. It also has low S (0.015 wt%) and relatively high Cl (180 ppm). We suggest that this unusual composition is a consequence of olivine trapping plagioclase in a hot, strongly plagioclase-undersaturated magma and subsequent reaction between plagioclase and the host olivine producing melt and residual spinel. Two other melt inclusions in a different olivine phenocryst have compositions that are generally intermediate between 'normal' inclusions and the aluminous inclusion, but have even higher CaO and Sr contents. They are also depleted in incompatible elements, but to a lesser degree than the aluminous inclusion, and have smaller Sr and Eu anomalies. Similar inclusions have also been described in high-Fo olivine phenocrysts from Iceland and northern Mid-Atlantic Ridge. We suggest that the compositions of these inclusions represent assimilation of gabbroic material into the hot primitive magma. The localised nature of this assimilation is consistent with it occurring within a crystal mush zone where the porosity is high as primitive magmas pass through earlier formed gabbroic 'cumulates'. In such an environment the contaminants are expected to have quite diverse compositions. Although the interaction of primitive melts with gabbroic material may not affect the compositions of erupted MORB melts on a large scale, this process may be important in some MORB suites and should be accounted for in petrogenetic models. Another important implication is that the observed variability in melt inclusion compositions in primitive MORB phenocrysts need not always to reflect processes occurring in the mantle. In particular, inferences on fractional melting processes based on geochemistry of ultra-depleted melt inclusions may not always be valid.  相似文献   

13.
Reequilibration of chromite within Kilauea Iki lava lake,Hawaii   总被引：11，自引：0，他引：11  
Chromite mainly occurs as tiny inclusions within or at the edges of olivine phenocrysts in the 1959 Kilauea Iki lava lake. Liquilus chromite compositions are only preserved in scoria that was rapidly quenched from eruption temperatures. Analyses of drill core taken from the lava lake in 1960, 1961, 1975, 1979, and 1981 show that chromite becomes richer in Fe+2, Fe+3, Ti and poorer in Mg, Al, Cr than the liquidus chromite. The amount of compositional change depends on the time elapsed since eruption, the cooling history of the sample, the extent of differentiation of the interstitial melt, and the position of the chromite inclusion within the olivine phenocryst. Compositional changes of the chromite inclusions are thought to be a result of reequilibration with the residual melt by cationic diffusion (Mg, Al, Cr outwards and Fe+2, Fe+3, Ti inwards) through olivine. The changing chemical potential gradients produced as the residual melt cools, crystallizes and differentiates drives the reequilibration process. Major and minor element zoning profiles in olivine phenocrysts suggest that volume diffusion through olivine may have been the major mechanism of cationic transport through olivine. The dramatic compositional changes observed in chromite over the 22 years between eruption and 1981 has major implications for othe molten bodies.  相似文献   

14.
In order to characterize the composition of the parental melts of intracontinental alkali-basalts, we have undertaken a study of melt and fluid inclusions in olivine crystals in basaltic scoria and associated upper mantle nodules from Puy Beaunit, a volcano from the Chaîne des Puys volcanic province of the French Massif Central (West-European Rift system). Certain melt inclusions were experimentally homogenised by heating-stage experiments and analysed to obtain major- and trace-element compositions. In basaltic scoria, olivine-hosted melt inclusions occur as primary isolated inclusions formed during growth of the host phase. Some melt inclusions contain both glass and daughter minerals that formed during closed-system crystallisation of the inclusion and consist mainly of clinopyroxene, plagioclase and rhönite crystals. Experimentally rehomogenised and naturally quenched, glassy inclusions have alkali-basalt compositions (with SiO2 content as low as 42 wt%, MgO>6 wt%, Na2O+K2O>5 wt%, Cl~1,000–3,000 ppm and S~400–2,000 ppm), which are consistent with those expected for the parental magmas of the Chaîne des Puys magmatic suites. Their trace-element signature is characterized by high concentration(s) of LILE and high LREE/HREE ratios, implying an enriched source likely to have incorporated small amounts of recycled sediments. In olivine porphyroclasts of the spinel peridotite nodules, silicate melt inclusions are secondary in nature and form trails along fracture planes. They are generally associated with secondary CO2 fluid inclusions containing coexisting vapour and liquid phases in the same trail. This observation and the existence of multiphase inclusions consisting of silicate glass and CO2-rich fluid suggest the former existence of a CO2-rich silicate melt phase. Unheated glass inclusions have silicic major-element compositions, with normative nepheline and olivine components, ~58 wt% SiO2, ~9 wt% total alkali oxides, <3 wt% FeO and MgO. They also have high chlorine levels (>3,000 ppm) but their sulphur concentrations are low (<200 ppm). Comparison with experimental isobaric trends for peridotite indicates that they represent high-pressure (~1.0 GPa) trapped aliquots of near-solidus partial melts of spinel peridotite. Following this hypothesis, their silica-rich compositions would reflect the effect of alkali oxides on the silica activity coefficient of the melt during the melting process. Indeed, the silica activity coefficient decreases with addition of alkalis around 1.0 GPa. For mantle melts coexisting with an olivine-orthopyroxene-bearing mineral assemblage buffering SiO2 activity, this decrease is therefore compensated by an increase in the SiO2 content of the melt. Because of their high viscosity and the low permeability of their matrix, these near-solidus peridotite melts show limited ability to segregate and migrate, which can explain the absence of a chemical relationship between the olivine-hosted melt inclusions in the nodules and in basaltic scoria.  相似文献   

15.
Melt inclusions in olivine and pyroxene phenocrysts in kersantite and camptonite at Chhaktalao in Madhya Pradesh, India are mainly of the evolved type forming daughter minerals of olivine, pyroxene, plagioclase, spinel, mica, titanomagnetite and sulphides. Heating studies exhibit a temperature range from 1215° to 1245°C for the melt inclusions in olivine in camptonite and 1220–1245°C for olivine in kersantite. The temperature for melt inclusions in pyroxene ranged from 1000° to 1150°C in camptonite and 850–1100°C for pyroxene in kersantite. The bubble inside these melt inclusions is mainly CO2. The Th°C of CO2 into liquid phase occurred between 26° and 31°C in olivine and 25–30°C in pyroxene from kersantite and camptonite. The maximum density estimated is 0.72 g/cm3 and the minimum is 0.45 g/cm3. The depth of entrapment of the melt inclusion is estimated between 10–15 km. The pressure of entrapment of melt inclusion in olvine is 4.6 kbar where as that in pyroxene is 3.7 kbar. The lamprophyres in the Chhaktalao area are considered to be derived from low depth and low pressure region, possibly within spinel lherzolite zone.  相似文献   

16.
《Chemical Geology》2007,236(3-4):303-322
In order to better understand what controls sulfur speciation in melt inclusions, and how that pertains to the original basalt composition, we have conducted a series of heating experiments on naturally quenched and crystalline olivine-hosted melt inclusions. Sulfur speciation was determined from S Kα peak shift measurements by electron microprobe on the experimentally heated inclusions as well as a series of naturally quenched inclusions, and matrix glasses.Naturally quenched olivine-hosted melt inclusions record a similar but more variable sulfur speciation relative to matrix glasses, (up to 45–50% variation in S6+/Stotal). Much of this range can be attributed to the effect of degassing which may either increase or decrease the S6+/Stotal. In addition, olivine melt re equilibration and H diffusion out of the inclusion both potentially result in the oxidation of melt inclusions. Heating of melt inclusions can have different effects on the sulfur speciation under different conditions. A slight decrease in S6+/Stotal and oxygen fugacity (∼0.1 log units) can occur from overheating of inclusions (above the temperature of entrapment), resulting from excess ferrous iron in the melt. An increase in heating times should result in an oxidation of the inclusion generated by increased H diffusion out of the inclusion. However, results of heating experiments on melt inclusions from an Izu backarc basalt for less than 30  min do not show a significant increase in sulfur oxidation. In addition, experiments conducted at both IW and FMQ have measured sulfur speciation consistent with naturally quenched inclusions suggesting that at experimental temperatures near that of olivine crystallization the furnace atmosphere does not exert significant control on the melt fO2. By taking these parameters into account, sulfur speciation and oxidation state of basaltic melt trapped within inclusions can be accurately determined from both naturally quenched and heated olivine hosted melt inclusions.  相似文献   

17.
This study presents a new experimental approach for determining H2O solubility in basaltic melt at upper mantle conditions. Traditional solubility experiments are limited to pressures of ~600 MPa or less because it is difficult to reliably quench silicate melts containing greater than ~10 wt% dissolved H2O. To overcome this limitation, our approach relies on the use of secondary ion mass spectrometry to measure the concentration of H dissolved in olivine and on using the measured H in olivine as a proxy for the concentration of H2O in the co-existing basaltic melt. The solubility of H2O in the melt is determined by performing a series of experiments at a single pressure and temperature with increasing amounts of liquid H2O added to each charge. The point at which the concentration of H in the olivine first becomes independent of the amount of initial H2O content of the charge (added + adsorbed H2O) indicates its solubility in the melt. Experiments were conducted by packing basalt powder into a capsule fabricated from San Carlos olivine, which was then pressure-sealed inside a Ni outer capsule. Our experimental results indicate that at 1000 MPa and 1200 °C, the solubility of H2O in basaltic melt is 20.6 ± 0.9 wt% (2 × standard deviation). This concentration is considerably higher than predicted by most solubility models but defines a linear relationship between H2O fugacity and the square of molar H2O solubility when combined with solubility data from lower pressure experiments. Further, our solubility determination agrees with melting point depression determined experimentally by Grove et al. (2006) for the H2O-saturated peridotite solidus at 1000 MPa. Melting point depression calculations were used to estimate H2O solubility in basalt along the experimentally determined H2O-saturated peridotite solidus. The results suggest that a linear relationship between H2O fugacity and the square of molar solubility exists up to ~1300 MPa, where there is an inflection point and solubility begins to increase less strongly with increasing H2O fugacity.  相似文献   

18.
The rate of water loss from olivine-hosted melt inclusions   总被引：1，自引：1，他引：0  
Diffusive water loss from olivine-hosted melt inclusions has been reported previously. This process must be considered when interpreting melt inclusion data. This study measured the rate of water loss from olivine-hosted melt inclusions during heating-stage experiments to test a previous diffusive reequilibration model and the hydrogen diffusion mechanism that controls the rate. Olivine-hosted melt inclusions were heated to a constant temperature in reduced Ar gas in a heating stage for a few hours, and unpolarized Fourier transform infrared spectra were repeatedly measured through the inclusions. Water loss occurred rapidly in the experiments. Within a few hours, the water absorbance at 3,500 cm−1 wavenumber decreased by half. The observed water loss rate can be explained by the diffusive reequilibration model and hydrogen diffusion in olivine coupled with metal vacancy. The beginning of water loss was different in the low- and high-temperature experiments. At low temperatures (1,423 and 1,437 K), water loss did not occur in the initial 1 or 2 h. At high temperatures (1,471–1,561 K), water loss began immediately. The initial time period without water loss at low temperatures may be explained by a hydrogen fugacity barrier in the host olivine. At low temperatures, the internal pressure may be lower than the equilibrium pressure of melt inclusion and olivine, causing lower hydrogen fugacity in the melt inclusion than in the olivine, which will delay the water loss from the melt inclusion. The tested model and diffusivity were used to estimate the rate of water loss during homogenization experiments and magma eruption and cooling. For 1-h homogenization experiment, the model shows that large inclusions (50 μm radius) in large olivines (500 μm radius) are robust against water loss, while large or small inclusions (50–10 μm radius) in small olivines (150 μm radius) may suffer 30–100% water loss. For natural samples, the correlation between water concentration and melt inclusion and olivine sizes may be helpful to infer the initial water concentration, degree of diffusive reequilibration, and magma cooling rate.  相似文献   

19.
Melt inclusion and host glass compositions from the easternend of the Southwest Indian Ridge show a progressive depletionin light rare earth elements (LREE), Na8 and (La/Sm)n, but anincrease in Fe8, from the NE (64°E) towards the SW (49°E).These changes indicate an increase in the degree of mantle meltingtowards the SW and correlate with a shallowing of the ridgeaxial depth and increase in crustal thickness. In addition,LREE enrichment in both melt inclusions and host glasses fromthe NE end of the ridge are compatible with re-fertilizationof a depleted mantle source. The large compositional variations(e.g. P2O5 and K2O) of the melt inclusions from the NE end ofthe ridge (64°E), coupled with low Fe8 values, suggest thatmelts from the NE correspond to a variety of different batchesof melts generated at shallow levels in the mantle melting column.In contrast, the progressively more depleted compositions andhigher Fe8 values of the olivine- and plagioclase-hosted meltinclusions at the SW end of the studied region (49°E), suggestthat these melt inclusions represent batches of melt generatedby higher degrees of melting at greater mean depths in the mantlemelting column. Systematic differences in Fe8 values betweenthe plagioclase- and the olivine-hosted melt inclusions in theSW end (49°E) of the studied ridge area, suggest that theplagioclase-hosted melt inclusions represent final batches ofmelt generated at the top of the mantle melting column, whereasthe olivine-hosted melt inclusions correspond to melts generatedfrom less depleted, more fertile mantle at greater depths. KEY WORDS: basalt; melt inclusions; olivine; plagioclase; Southwest Indian Ridge  相似文献   

20.
Melt and fluid inclusions have been studied in olivine phenocrysts (Fo 81–79) from trachybasalts of the Southern Baikal volcanic area, Dzhida field. The melt inclusions were homogenized, quenched, and analyzed on an electron and ion microprobe. The study of homogenized glasses of nine inclusions showed that basaltic melts (SiO2 = 47.1–50.3 wt %, MgO = 5.0–7.7 wt %, CaO = 7.1–11.1 wt %) have high contents of Al2O3 (17.1–19.6 wt %), Na2O (4.1–6.2 wt %), K2O (2.2–3.3 wt %), and P2O5 (0.6–1.1 wt %). The volatile contents are low (in wt %): 0.24–0.31 H2O, 0.08 F, 0.03 Cl, and 0.02 S. Primary fluid inclusions in olivines from four trachybasalt samples contain high-density CO2 (0.73–0.87 g/cm3), indicating a CO2 fluid pressure of 4.3–6.6 kbar at 1200–1300°C and olivine crystallization depths of 16–24 km. Ion microprobe analyses of 20 glasses from melt inclusions for trace elements showed that the magmas of the Baikal rift were enriched in incompatible elements, thus differing from oceanic rift basalts and resembling oceanic island basalts. A comparison of our data on melt and fluid inclusions in olivine from trachybasalts of the Dzhida field with preexisting data on the Eastern Tuva volcanic highland in the Southern Baikal volcanic area showed that they had similar contents of volatiles, major, and trace elements.  相似文献   

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