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1.
The crystallization sequence of a basaltic andesite from Bezymianny Volcano, Kamchatka, Russia, was simulated experimentally at 100 and 700 MPa at various water activities (aH2O) to investigate the compositional evolution of residual liquids. The temperature (T) range of the experiments was 950–1,150 °C, aH2O varied between 0.1 and 1, and the log of oxygen fugacity (fO2) varied between quartz–fayalite–magnetite (QFM) and QFM + 4.1. The comparison of the experimentally produced liquids and natural samples was used to constrain the pressure (P)–T–aH2O–fO2 conditions of the Bezymianny parental magma in the intra-crustal magma plumbing system. The phase equilibria constraints suggest that parental basaltic andesite magmas should contain ~2–2.5 wt% H2O; they can be stored in upper crustal levels at a depth of ~15 km, and at this depth they start to crystallize at ~1,110 °C. The subsequent chemical evolution of this parental magma most probably proceeded as decompressional crystallization occurred during magma ascent. The final depths at which crystallization products accumulated prior to eruption are not well constrained experimentally but should not be shallower than 3–4 km because amphibole is present in natural magmas (>150 MPa). Thus, the major volume of Bezymianny andesites was produced in a mid-crustal magma chamber as a result of decompressional crystallization of parental basaltic andesites, accompanied by mixing with silicic products from the earlier stages of magma fractionation. In addition, these processes are complicated by the release of volatiles due to magma degassing, which occurs at various stages during magma ascent.  相似文献   

2.
《Comptes Rendus Geoscience》2014,346(7-8):190-199
Melt inclusions (MIs) in quartz from granitoids in the northern Qinling belt were studied using microthermometry and laser Raman spectroscopy. The total homogenization of melt inclusions occurs in a mean range between 1050 and 1100 °C. Laser Raman experiments reveal H2O, C2H6, C4H6 and CH4 as the dominant volatile compounds. Our results provide insights into the temperatures of magma crystallization and the dominantly reducing environment during the early magmatic stage. Based on ore mineralogy, and on the volatile species content in the MIs, we evidence firstly that the Qiushuwan porphyry Cu–Mo deposit in the Qinling–Dabie–Sulu orogenic belt was derived from a reduced magmatic system, emplaced at relatively deep domains more than 10 km deep, and secondly, that the magmas that are responsible for the generation of Qiushuwan were either derived from an inherently reduced source, or reduced during ascent and emplacement. The mechanism might have involved the assimilation of sedimentary material with minimal crustal interaction. The parental magmas likely underwent reduction essentially by loss of all of their SO2 by degassing, as evidenced by the low S content in melt inclusions. These reduced materials provided adequate sulfur source for the formation of the porphyry Cu–Mo deposits with obvious zonation, which plays a key role in the mineralization; finally, we conclude that the reduced environment and the relatively deep domain of magma emplacement probably limited the extent of mineralization, generating only a relatively small Cu–Mo deposit in Qiushuwan, located within the northern Qinling accretionary belt.  相似文献   

3.
Volatiles contribute to magma ascent through the sub-volcanic plumbing system. Here, we investigate melt inclusion compositions in terms of major and trace elements, as well as volatiles (H2O, CO2, SO2, F, Cl, Br, S) for Quaternary Plinian and dome-forming dacite and andesite eruptions in the central and the northern part of Dominica (Lesser Antilles arc). Melt inclusions, hosted in orthopyroxene, clinopyroxene and plagioclase are consistently rhyolitic. Post-entrapment crystallisation effects are limited, and negligible in orthopyroxene-hosted inclusions. Melt inclusions are among the most water-rich yet recorded (≤?8 wt% H2O). CO2 contents are generally low (<?650 ppm), although in general the highest pressure melt inclusion contain the highest CO2. Some low-pressure (<?3 kbars) inclusions have elevated CO2 (up to 1100–1150 ppm), suggestive of fluxing of shallow magmas with CO2-rich fluids. CO2-trace element systematics indicate that melts were volatile-saturated at the time of entrapment and can be used for volatile-saturation barometry. The calculated pressure range (0.8–7.5 kbars) indicates that magmas originate from a vertically-extensive (3–27 km depth) storage zone within the crust that may extend to the sub-Dominica Moho (28 km). The vertically-extensive crustal system is consistent with mush models for sub-volcanic arc crust wherein mantle-derived mafic magmas undergo differentiation over a range of crustal depths. The other volatile range of composition for melt inclusions from the central part is F (75–557 ppm), Cl (1525–3137 ppm), Br (6.1–15.4 ppm) and SO2 (<?140 ppm), and for the northern part it’s F (92–798 ppm), Cl (1506–4428 ppm), Br (not determined) and SO2 (<?569; one value at 1015 ppm). All MIs, regardless of provenance, describe the same Cl/F correlation (8.3?±?2.7), indicating that the magma source at depth is similar. The high H2O content of Dominica magmas has implications for hazard assessment.  相似文献   

4.
Significant zonation in major, minor, trace, and volatile elements has been documented in naturally glassy olivine-hosted melt inclusions from the Siqueiros Fracture Zone and the Galapagos Islands. Components with a higher concentration in the host olivine than in the melt (e.g., MgO, FeO, Cr2O3, and MnO) are depleted at the edges of the zoned melt inclusions relative to their centers, whereas except for CaO, H2O, and F, components with a lower concentration in the host olivine than in the melt (e.g., Al2O3, SiO2, Na2O, K2O, TiO2, S, and Cl) are enriched near the melt inclusion edges. This zonation is due to formation of an olivine-depleted boundary layer in the adjacent melt in response to cooling and crystallization of olivine on the walls of the melt inclusions, concurrent with diffusive propagation of the boundary layer toward the inclusion center. Concentration profiles of some components in the melt inclusions exhibit multicomponent diffusion effects such as uphill diffusion (CaO, FeO) or slowing of the diffusion of typically rapidly diffusing components (Na2O, K2O) by coupling to slow diffusing components such as SiO2 and Al2O3. Concentrations of H2O and F decrease toward the edges of some of the Siqueiros melt inclusions, suggesting either that these components have been lost from the inclusions into the host olivine late in their cooling histories and/or that these components are exhibiting multicomponent diffusion effects. A model has been developed of the time-dependent evolution of MgO concentration profiles in melt inclusions due to simultaneous depletion of MgO at the inclusion walls due to olivine growth and diffusion of MgO in the melt inclusions in response to this depletion. Observed concentration profiles were fit to this model to constrain their thermal histories. Cooling rates determined by a single-stage linear cooling model are 150–13,000 °C h?1 from the liquidus down to ~1,000 °C, consistent with previously determined cooling rates for basaltic glasses; compositional trends with melt inclusion size observed in the Siqueiros melt inclusions are described well by this simple single-stage linear cooling model. Despite the overall success of the modeling of MgO concentration profiles using a single-stage cooling history, MgO concentration profiles in some melt inclusions are better fit by a two-stage cooling history with a slower-cooling first stage followed by a faster-cooling second stage; the inferred total duration of cooling from the liquidus down to ~1,000 °C ranges from 40 s to just over 1 h. Based on our observations and models, compositions of zoned melt inclusions (even if measured at the centers of the inclusions) will typically have been diffusively fractionated relative to the initially trapped melt; for such inclusions, the initial composition cannot be simply reconstructed based on olivine-addition calculations, so caution should be exercised in application of such reconstructions to correct for post-entrapment crystallization of olivine on inclusion walls. Off-center analyses of a melt inclusion can also give results significantly fractionated relative to simple olivine crystallization. All melt inclusions from the Siqueiros and Galapagos sample suites exhibit zoning profiles, and this feature may be nearly universal in glassy, olivine-hosted inclusions. If so, zoning profiles in melt inclusions could be widely useful to constrain late-stage syneruptive processes and as natural diffusion experiments.  相似文献   

5.
The Yangla copper deposit, with Cu reserves of 1.2 Mt, is located between a series of thrust faults in the Jinshajiang–Lancangjiang–Nujiang region, Yunnan, China, and has been mined since 2007. Fluid inclusion trapping conditions ranged from 1.32 to 2.10 kbar at 373–409 °C. Laser Raman spectroscopy confirms that the vapour phase in these inclusions consists of CO2, CH4, N2 and H2O. The gas phases in the inclusions are H2O and CO2, with minor amounts of N2, O2, CO, CH4, C2H2, C2H4, and C2H6. Within the liquid phase, the main cations are Ca2+ and Na+ while the main anions are SO4 2? and Cl?. The oxygen and hydrogen isotope compositions of the ore-forming fluids (?3.05‰?≤?δ18OH2O?≤?2.5‰; ?100‰?≤?δD?≤??120‰) indicate that they were derived from magma and evolved by mixing with local meteoric water. The δ34S values of sulfides range from ?4.20‰ to 1.85‰(average on ?0.85‰), supporting a magmatic origin. Five molybdenite samples taken from the copper deposit yield a well-constrained 187Re–187Os isochron age of 232.8?±?2.4 Ma. Given that the Yangla granodiorite formed between 235.6?±?1.2 Ma and 234.1?±?1.2 Ma, the Cu metallogenesis is slightly younger than the crystallization age of the parent magma. A tectonic model that combines hydrothermal fluid flow and isotope compositions is proposed to explain the formation of the Yangla copper deposit. At first, westward subduction of the Jinshajiang Oceanic Plate in the Early Permian resulted in the development of a series of thrust faults. This was accompanied by fractional melting beneath the overriding plate, triggering magma ascent and extensive volcanism. The thrust faults, which were then placed under tension during a change in tectonic mode from compression to extension in the Late Triassic, formed favorable pathways for the magmatic ore-forming fluids. These fluids precipitated copper-sulfides to form the Yangla deposit.  相似文献   

6.
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   

7.
ABSTRACT

The Xiaohaizi wehrlite intrusion in the early Permian Tarim Large Igneous Province, Northwest China, is characterized by unusual high-An (up to 86) plagioclases. It has been suggested that H2O may have exerted a major control on their formation, but this interpretation requires further direct evidence. Moreover, it remains unclear where the water came from. In order to unravel these questions, we present electron microprobe analyses of minerals and melt inclusions in clinopyroxene macrocrysts in the dikes crosscutting the Xiaohaizi wehrlite intrusion and in situ oxygen isotope data of zircons from the Xiaohaizi wehrlite. The homogenized melt inclusions have restricted SiO2 (45.5–48.7 wt.%) and Na2O + K2O (2.4–3.8 wt.%) contents, displaying sub-alkaline affinity. This is inconsistent with the alkaline characteristic of the parental magma of the clinopyroxenes, suggesting significant modification of melt inclusions by contamination of the host clinopyroxene due to overheating. Nevertheless, the Ca/Na ratios (2.9–4.7) of melt inclusions are the upper limit of the parental magma of the clinopyroxenes due to high CaO (21.5–23.0 wt.%) and very low Na2O (0.22–0.34 wt.%) contents in the host clinopyroxenes. Thermodynamic calculation suggests that under fixed P (2.7 kbar) and T (1000°C), and assumed H2O (~1.5 wt.%) conditions, the Ca/Na ratio of the parental magma cannot generate high-An plagioclase in the wehrlite. The results confirm that H2O exerts a major control. Zircon δ18O (VSMOW) values (2.99–3.71‰) are significantly lower than that of mantle-derived zircon (5.3 ± 0.6‰). Such low zircon δ18O values may be due to incorporation of large amounts of low-δ18O, hydrothermally altered oceanic crust. However, geochemical and Sr-Nd-Pb isotopic data do not support recycled oceanic crust in the mantle source of the Xiaohaizi intrusion. Alternatively this can be explained by incorporation of meteoritic water in the magma chamber. This will increase the H2O content of the liquid that finally crystallize high-An plagioclases.  相似文献   

8.
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   

9.
The conditions under which rear-arc magmas are generated were estimated using primary basalts from the Sannome-gata volcano, located in the rear of the NE Japan arc. Scoriae from the volcano occur with abundant crustal and mantle xenoliths, suggesting that the magma ascended rapidly from the upper mantle. The scoriae show significant variations in their whole-rock compositions (7.9–11.1 wt% MgO). High-MgO scoriae (MgO > ~9.5 wt%) have mostly homogeneous 87Sr/86Sr ratios (0.70318–0.70320), whereas low-MgO scoriae (MgO < ~9 wt%) have higher 87Sr/86Sr ratios (>0.70327); ratios tend to increase with decreasing MgO content. The high-MgO scoriae are aphyric, containing ~5 vol% olivine microphenocrysts with Mg# [100 × Mg/(Mg + Fe2+)] of up to 90. In contrast, the low-MgO scoriae have crustal xenocrysts of plagioclase, alkali feldspar, and quartz, and the mineralogic modes correlate negatively with whole-rock MgO content. On the basis of these observations, it is inferred that the high-MgO scoriae represent primary or near-primary melts, while the low-MgO scoriae underwent considerable interaction with the crust. Using thermodynamic analysis of the observed petrological features of the high-MgO scoriae, the eruption temperature of the magmas was constrained to 1,160–1,220 °C. Given that the source mantle was depleted MORB-source mantle, the primary magma was plausibly generated by ~7 % melting of a garnet-bearing spinel peridotite; taking this into consideration, and considering the constraints of multi-component thermodynamics, we estimated that the primary Sannome-gata magma was generated in the source mantle with 0.5–0.6 wt% H2O at 1,220–1,230 °C and at ~1.8 GPa, and that the H2O content of the primary magma was 6–7 wt%. The rear-arc Sannome-gata magma was generated by a lower degree of melting of the mantle at greater depths and lower temperatures than the frontal-arc magma from the Iwate volcano, which was also estimated to be generated by ~15 % melting of the source mantle with 0.6–0.7 wt% H2O at ~1,250 °C and at ~1.3 GPa.  相似文献   

10.
《International Geology Review》2012,54(10):1179-1190
Andesite magmatism plays a major role in continental crustal growth, but its subduction-zone origin and evolution is still a hotly debated topic. Compared with whole-rock analyses, melt inclusions (MIs) can provide important direct information on the processes of magma evolution. In this article, we synthesize data for melt inclusions hosted by phenocrysts in andesites, extracted from the GEOROC global compilation. These data show that melt inclusions entrapped by different phenocrysts have distinct compositions: olivine-hosted melt inclusions have basalt and basaltic andesite compositions, whereas melt inclusions in clinopyroxene and othopyroxene are mainly dacitic to rhyolitic. Hornblende-hosted melt inclusions have rhyolite composition. The compositions of melt inclusions entrapped by plagioclase are scattered, spanning from andesite to rhyolite. On the basis of the compositional data, we propose a mixing model for the genesis of the andesite, and a two-chamber mechanism to account for the evolution of the andesite. First, andesite melt is generated in the lower chamber by mixing of a basaltic melt derived from the mantle and emplaced in the lower crust with a felsic melt resulting from partial melting of crustal rocks. Olivine and minor plagioclase likely crystallize in the lower magma chamber. Secondly, the andesite melt ascends into the upper chamber where other phenocrysts crystallize. According to SiO2-MgO diagrams of the MIs, evolution of the andesite in the upper chamber can be subdivided into two distinct stages. The early stage (I) is characterized by a phenocrystal assemblage of clinopyroxene + othopyroxene + plagioclase, whereas the late stage (II) is dominated by crystallization of plagioclase + hornblende.  相似文献   

11.
Hydrogen defect saturation in natural pyroxene   总被引：1，自引：0，他引：1  
Dehydration via the redox reaction: OH? + Fe2+ ? O2? + Fe3+ + ½H2 is believed to be a commonly occurring process in pyroxenes and other nominally anhydrous minerals (NAMs) from the upper mantle and appears to be fast enough to allow significant dehydration during magma ascent. Nevertheless, the mobility of hydrogen incorporating defects is controlled by cation diffusion with approximately two orders of magnitude slower reaction kinetics than the iron redox reaction, and host defects have a much higher likelihood to be preserved than the hydrogen itself. Therefore, restoring hydrogen into the structure would be possible by driving the redox reaction backwards, as long as temperature and time are limited so as not to change the defect state of the crystal structure. Here we investigate the re-hydration capacity of megacryst and xenocryst ortho- and clinopyroxene by stepwise thermal annealing of crystallographically oriented samples in 1 atm H2. H concentration was measured by FTIR spectroscopy after each annealing step. Most samples show only a small increase in water content up to a presumed saturation level, after which further heat treatments in H2 resulted in a slight decrease in water contents. However, two of the studied samples, both fairly Fe rich megacrysts, are significantly rehydrated. Some samples or crystal sections exhibit a practically inert behavior, with minor fluctuations around initial water concentrations. Present results indicate that most mantle pyroxenes have not been substantially dehydrated during late stage magma processes, and that restoring water is possible in samples which have lost considerable amounts of water.  相似文献   

12.
Changes in magmatic assemblages and crystal stability as a response of CO2-flushing in basaltic systems have rarely been directly addressed experimentally, making the role of CO2 in magma dynamics still controversial and object of scientific debate. We conducted a series of experiments to understand the response of magmas from Etna volcano to CO2 flushing. We performed a first experiment at 300 MPa to synthesize a starting material composed of crystals of some hundreds of µm and melt pools. This material is representative of an initial magmatic assemblage composed of plagioclase, clinopyroxene and a water-undersaturated melt with 1.6 wt% H2O. In a second step, the initial assemblage was equilibrated at 300 and 100 MPa with fluids having different XCO 2 fl (CO2/(H2O + CO2)). At low XCO 2 fl (< 0.2 to 0.4), plagioclase is completely dissolved and clinopyroxene show dissolution textures. For relatively high XCO 2 fl (0.9 at 300 MPa), the flushing of a CO2-rich fluid phase leads to an increase of the amount of clinopyroxene and a decrease of the abundance of plagioclase at 300 MPa. This decrease of plagioclase proportion is associated with a change in An content. Our experiments demonstrate that flushing basaltic systems with fluids may drastically affect crystal textures and phase equilibria depending on proportions of H2O and CO2 in the fluid phase. Since texture and crystal proportions are among the most important parameters governing the rheology of magmas, fluid flushing will also influence magma ascent to the Earth’s surface. The experimental results open new perspectives to decipher the textural and compositional record of minerals observed in volcanic rocks from Mt. Etna, and at the same time offer the basis for interpreting the information preserved in minerals from other basaltic volcanoes erupting magmas enriched in CO2.  相似文献   

13.
Kinetic and fluid dynamic constraints on deep-seated magma migration rates suggest ascent velocities in the range 10 to 30 m/s, 10–1 to 10 m/s and 10–2 to 5 m/s for kimberlitic, garnet peridotite-bearing and spinel peridotite-bearing alkalic magmas. These rates virtually demand translithospheric magma transport by a fracture as opposed to diapiric mechanism. The hypothesis that volatile exsolution accelerates magma through the deep lithosphere is tested by solution of the appropriate set of conservation, mass balance and volatile component solubility equations governing the steady ascent (decompression) of compressible, two-phase magma (melt+H2O+CO2) in which irreversible phenomena (friction, heat transfer) are accounted for. The results of the numerical experiments were designed to test the importance of melt bulk composition (kimberlite, nephelinite, alkali basalt), initial conditions (mass flux (M), heat transfer coefficient (B), lumped friction factor (C f )), conduit width (D), initial magma volatile content and geothermal gradients. The fractional increase in ascent rate (u/u i ) is rarely greater than approximately 2 during translithospheric migration. The propellant hypothesis is rejected as a first-order mechanism driving magma acceleration during ascent. The most influential parameters governing ascent dynamics are M, C f , D, B and the geotherm. Because of the relatively incompressible nature of the magmatic volatile phase at P>100 MPa, the initial magma volatile content plays a secondary (although demonstrable) role. The main role of volatiles is in controlling the initial magma flux (M) and the magma pressure during ascent. In adiabatic (B=0) simulations, magma ascends nearly isothermally. Generally, however, the assumption of adiabaticity is a poor one especially for flow through narrow (0.5 to 2 m) conduits in old (cold) lithosphere at rates 10–1 m/s. The proposed fluid dynamic model is consistent with and complementary to the magma-driven crack propagation models. The generation of mantle metasomatic fluid is a corollary of the non-adiabatic ascent of volatile-bearing magma through the lithosphere. Magma heat death is an important process for the creation of mantle heterogeneity.  相似文献   

14.
Fourier transform infrared spectrometry (FTIR) analyses of olivines from peridotite xenoliths found in southern African kimberlites indicate 0 to 80 ppm H2O concentrations. OH absorbance profiles across olivine grains show homogeneous H contents from core to edge for most samples. In one sample the olivines are H-free, while another has olivines characterized by lower H contents at the grain edges compared to the cores, indicating H loss during transport of the xenolith to the surface. Flat or near-flat H profiles place severe constraints on the duration of H loss from olivine grains, with implications for kimberlite magma ascent rates. Diffusion equations were used to estimate times of H loss of about 4 h for the sample with heterogeneous olivine H contents. Resulting kimberlite ascent rates are calculated to be 5-37 m s−1 minimum, although these estimates are highly dependent on volatile contents and degassing behavior of the host kimberlite magma. Xenolithic olivines from alkali basalts generally have lower H contents and more pronounced H diffusion profiles than do those from kimberlites. This difference is likely caused by higher magma temperatures and lower ascent rates of alkali basalts compared to kimberlites.  相似文献   

15.
Buoyancy controls the ability of magma to rise, its ascent rate and the style of the eruptions. Geophysical, geological and petrological data have been integrated to evaluate the buoyancy of magmas at Mt Etna. The density difference between host rocks and magmas is mainly related to the amount of H2O dissolved in the magma and to the bubble‐liquid separation processes. In the depth interval 22–2 km b.s.l. highly hydrated (H2O ～ 3%) basaltic magmas or mixtures of bubbles + liquid have positive buoyancy and rise rapidly. Conversely, bubble‐depleted liquids, with an intermediate H2O content (～ 1.5%), having neutral buoyancy, will spread out and form magmatic reservoirs at different depths until cooling/crystallization further modify composition and density. These different processes account for the magma compositions, location of magmatic reservoirs as determined by geophysical methods, and the complex eruptive cycles (slow effusions, fire fountains and Plinian eruptions) that have been observed in the history of the volcano.  相似文献   

16.
Diffusive coarsening (Ostwald ripening) of H2O and H2O-CO2 bubbles in rhyolite and basaltic andesite melts was studied with elevated temperature–pressure experiments to investigate the rates and time spans over which vapor bubbles may enlarge and attain sufficient buoyancy to segregate in magmatic systems. Bubble growth and segregation are also considered in terms of classical steady-state and transient (non-steady-state) ripening theory. Experimental results are consistent with diffusive coarsening as the dominant mechanism of bubble growth. Ripening is faster in experiments saturated with pure H2O than in those with a CO2-rich mixed vapor probably due to faster diffusion of H2O than CO2 through the melt. None of the experimental series followed the time1/3 increase in mean bubble radius and time−1 decrease in bubble number density predicted by classical steady-state ripening theory. Instead, products are interpreted as resulting from transient regime ripening. Application of transient regime theory suggests that bubbly magmas may require from days to 100 years to reach steady-state ripening conditions. Experimental results, as well as theory for steady-state ripening of bubbles that are immobile or undergoing buoyant ascent, indicate that diffusive coarsening efficiently eliminates micron-sized bubbles and would produce mm-sized bubbles in 102–104 years in crustal magma bodies. Once bubbles attain mm-sizes, their calculated ascent rates are sufficient that they could transit multiple kilometers over hundreds to thousands of years through mafic and silicic melt, respectively. These results show that diffusive coarsening can facilitate transfer of volatiles through, and from, magmatic systems by creating bubbles sufficiently large for rapid ascent.  相似文献   

17.
Uturuncu is a dormant volcano in the Altiplano of SW Bolivia. A present day ~70 km diameter interferometric synthetic aperture radar (InSAR) anomaly roughly centred on Uturuncu’s edifice is believed to be a result of magma intrusion into an active crustal pluton. Past activity at the volcano, spanning 0.89 to 0.27 Ma, is exclusively effusive and almost all lavas and domes are dacitic with phenocrysts of plagioclase, orthopyroxene, biotite, ilmenite and Ti-magnetite plus or minus quartz, and microlites of plagioclase and orthopyroxene set in rhyolitic groundmass glass. Plagioclase-hosted melt inclusions (MI) are rhyolitic with major element compositions that are similar to groundmass glasses. H2O concentrations plotted versus incompatible elements for individual samples describe a trend typical of near-isobaric, volatile-saturated crystallisation. At 870 °C, the average magma temperature calculated from Fe–Ti oxides, the average H2O of 3.2 ± 0.7 wt% and CO2 typically <160 ppm equate to MI trapping pressures of 50–120 MPa, approximately 2–4.5 km below surface. Such shallow storage precludes the role of dacite magma emplacement into pre-eruptive storage regions as being the cause of the observed InSAR anomaly. Storage pressures, whole-rock (WR) chemistry and phase assemblage are remarkably consistent across the eruptive history of the volcano, although magmatic temperatures calculated from Fe–Ti oxide geothermometry, zircon saturation thermometry using MI and orthopyroxene-melt thermometry range from 760 to 925 °C at NNO ± 1 log. This large temperature range is similar to that of saturation temperatures of observed phases in experimental data on Uturuncu dacites. The variation in calculated temperatures is attributed to piecemeal construction of the active pluton by successive inputs of new magma into a growing volume of plutonic mush. Fluctuating temperatures within the mush can account for sieve-textured cores and complex zoning in plagioclase phenocrysts, resorption of quartz and biotite phenocrysts and apatite microlites. That Fe–Ti oxide temperatures vary by ~50–100 °C in a single thin section indicates that magmas were not homogenised effectively prior to eruption. Phenocryst contents do not correlate with calculated magmatic temperatures, consistent with crystal entrainment from the mush during magma ascent and eruption. Microlites grew during ascent from the magma storage region. Variability in the proportion of microlites is attributed to differing ascent and effusion rates with faster rates in general for lavas >0.5 Ma compared to those <0.5 Ma. High microlite contents of domes indicate that effusion rates were probably slowest in dome-forming eruptions. Linear trends in WR major and trace element chemistries, highly variable, bimodal mineral compositions, and the presence of mafic enclaves in lavas demonstrate that intrusion of more mafic magmas into the evolving, shallow plutonic mush also occurred further amplifying local temperature fluctuations. Crystallisation and resorption of accessory phases, particularly ilmenite and apatite, can be detected in MI and groundmass glass trace element covariation trends, which are oblique to WRs. Marked variability of Ba, Sr and La in MI can be attributed to temperature-controlled, localised crystallisation of plagioclase, orthopyroxene and biotite within the evolving mush.  相似文献   

18.
We present data on volatile (S, F and Cl) and major element contents in olivine-hosted melt inclusions (MIs) from alkaline basaltic tephras along the Quaternary Payenia backarc volcanic province (~34°S–38°S) of the Andean Southern Volcanic Zone (SVZ). The composition of Cr-spinel inclusions and host olivines in Payenia are also included to constrain any variations in oxygen fugacity. The variation of potassium, fluorine and chlorine in MIs in Payenia can be modelled by partial melting (1–10%) of a variously metasomatised mantle. The high chlorine contents in MIs (up to 3200 ppm) from Northern Payenia require addition of subduction-related fluids to a mantle wedge, whereas volatile signatures in the southern Payenia are consistent with derivation from an enriched OIB source. Cl and Cl/K ratios define positive correlations with host olivine fosterite content (Fo80-90) that cannot be explained by olivine fractionation, degassing and/or degree of mantle melting. Neither can the correlation between SiO2 and TiO2 in the MIs and host olivine Fo-content be explained by magmatic differentiation processes. Instead these correlations essentially require a south to north mantle source transition from a low Mg# pyroxenite (from recycled eclogite) to a high Mg# fluid metasomatised peridotite. The Cl/K and S/K ratios in Payenia MIs extend from enriched OIB-like signatures (south) to Andean SVZ arc like signatures (north). We show that the northward increase in S, Cl and S/K is coupled to a northward increase in melt oxidation states and thus in Fe3+/Fetot ratios in the magmas. The increase in oxidation state also correlates with an increase of Mn/Fe (olivine) ratios. We calculate that 25% of the apparent north–south pyroxenite–peridotite source variation in Payenia (based on olivine Mn/Fe ratios) can be explained by the south to north variation in melt oxidation states.  相似文献   

19.
We have calculated the amounts of CO2 and H2 produced by complete degassing of mid-ocean ridge basalt (MORB) magma, and by degassing during transient diking-eruptive events. Our CO2 calculations are based on a model estimate of an initial CO2 content of 1800 ppm in MORB magma, which is equivalent to 2.2 × 1012 mol CO2 per year for magma production at worldwide ocean ridges. Observations indicate that many MORB magmas are emplaced in numerous small pulses of dikes and associated lava flows with very short emplacement times, which would result in release of relatively large amounts of CO2 over short intervals. For example, a dike injected into the oceanic crust that extends from the top of its magma chamber at 2 km depth to the seafloor would degas 2.3 × 104 mol CO2 per m2 surface area of dike, and produce another 4.0 × 104 mol CO2 per m2 on complete crystallization.

Unlike CO2, which is not strictly governed by crystallization-alteration processes, H2 is produced from MORB by the reduction of H2O by ferrous iron in the magma to form magnetite and H2 as the magma cools and crystallizes. From published paired analyses of MORB glass and crystalline rock, we estimate that the amount of H2 produced from one cubic meter of rock averages 301 mol. We suggest that the oxidizing agent is H2O dissolved in the magma, which results in rapid generation of H2. The amount of pre-alteration oxidation may be limited by the amount of H2O dissolved in the magma; thus relatively water-rich magmas will undergo greater oxidation. For the case of the two-kilometer-high dike reaching the seafloor, the amount of H2 released is 6.2 × 105 moles H2 per m2 surface area of the dike. This is 10 times greater than the total CO2 released by degassing and crystallization of the dike. Assuming that the H2 generation rate for the entire basaltic layer of the oceanic crust is the same as for MORB lavas (312 mol/m3), then the annual global H2 production rate is 6.3 × 1012 mol H2 per year. This amount is about three times greater than our calculated annual CO2 production from MORBs. Given that the annual CO2 production rate from MORBs over 3.3 Ga can account for all CO2 found in the Earth's crust, hydrosphere, and atmosphere, it is likely that the H2 produced at mid-ocean ridges plays a significant role as a reducing agent in the global redox state of the Earth's surface.

In contrast to time-averaged global production rates, the rapid release of CO2 and H2 in diking-eruptive events may locally result in formation of a separate gas phase containing H2-CO2-H2O in that order of abundance. The amounts of CO2 and H2 produced could provide a significant energy source for autotrophic microorganisms. It has been demonstrated that such a CO2-H2-H2O gas mixture yields methanol in magnetite-surface catalyzed reactions at seafloor hydrothermal conditions. Such abiotic synthesis reactions could have been important in early Earth processes.  相似文献   

20.
Quartz crystals from topaz–zinnwaldite–albite granites from Zinnwald (Erzgebirge, Germany) contain, in addition to primary and secondary fluid inclusions (FIs), abundant crystalline silicate-melt inclusions (MIs) with diameters up to 200 m. These MIs represent various stages of evolution of a highly evolved melt system that finally gave rise to granite-related Sn–W mineralization. The combination of special experimental techniques with confocal laser Raman-microprobe spectroscopy and EMPA permits precise measurement of elevated contents of H2O, F, and B in re-homogenized MIs. The contents of H2O and F were observed to increase from 3 to 30 and 1.9 to 6.4 wt%, respectively, during magma differentiation. However, there is a second MI group, very rich in H2O, with values up to 55 wt% H2O and an F concentration of approximately 3 wt%. Ongoing enrichment of volatiles H2O, F, B, and Cl and of Cs and Rb can be explained in terms of magma differentiation triggered by fractional crystallization and thus, is suggested to reflect elemental abundances in natural magmas, and not boundary-layer melts. Partitioning between melt and cogenetic fluids has further modified the magmatic concentrations of some elements, particularly Sn. The coexistence of two types of MIs with primary FIs indicates fluid saturation early in the history of magma crystallization, connected with a continuous sequestration of Sn, F, and B. The results of this study provide additional evidence for the extraordinary importance of the interplay of H2O, F, and B in the enrichment of Sn during magma differentiation by decreasing the viscosity of and increasing the diffusivity in the melts as well as by the formation of various stable fluoride complexes in the melt and coexisting fluid.
Rainer ThomasEmail: Phone: +49-331-2881474
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