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1.
The anionic structure of magmatic liquids has been estimated at 1 atm and at pressures corresponding to those of the upper mantle. These estimates are based predominantly on spectroscopic data on binary metal oxide-silica and ternary metal oxide-silica-alumina melts. Structural information on melt compositions in aluminate-silica joins has been used to provide detailed information on the role of Al3+ in natural magma at atmospheric and high pressure.Regardless of pressure, andesitic melts may be described as combinations of chain, sheet, and three-dimensional network units. Nearly all Al3+ in the magmatic liquid resides in the three-dimensional network units. This Al3+ is locally charge-balanced with Na+, K+, Ca2+, and Mg2+. In the latter two cases, Al3+ and Si4+ are ordered, whereas for Na+ and K+, Si4+ and Al3+ are randomly mixed. Solution of water in natural magma results in the formation of new nonbridging oxygens in addition to OH groups attached to Si4+ and metal cations.On the basis of determined solution mechanisms of CO2 and H2O in silicate melts, thermodynamic properties of HO+CO2, fluids and hydrous silicate melts and melting phase relations in peridotite-H2O-CO2, systems, it is found that natural andesitic magma in equilibrium with spinel Iherzolite in the upper mantle (10–20 kbar) must contain at least 5–7 wt.% H2O. Andesitic magma with 5–7 wt.% H2O in solution may be described as a mixture of Al-free three-dimensional units, sheets, and chains with a small proportion (less than 10%) of monomers.  相似文献   

2.
The combination of magnetotelluric survey and laboratory measurements of electrical conductivity is a powerful approach for exploring the conditions of Earth’s deep interior. Electrical conductivity of hydrous silicate melts and aqueous fluids is sensitive to composition, temperature, and pressure, making it useful for understanding partial melting and fluid activity at great depths. This study presents a review on the experimental studies of electrical conductivity of silicate melts and aqueous fluids, and introduces some important applications of experimental results. For silicate melts, electrical conductivity increases with increasing temperature but decreases with pressure. With a similar Na+ concentration, along the calc-alkaline series electrical conductivity generally increases from basaltic to rhyolitic melt, accompanied by a decreasing activation enthalpy. Electrical conductivity of silicate melts is strongly enhanced with the incorporation of water due to promoted cation mobility. For aqueous fluids, research is focused on dilute electrolyte solutions. Electrical conductivity typically first increases and then decreases with increasing temperature, and increases with pressure before approaching a plateau value. The dissociation constant of electrolyte can be derived from conductivity data. To develop generally applicable quantitative models of electrical conductivity of melt/fluid addressing the dependences on temperature, pressure, and composition, it requires more electrical conductivity measurements of representative systems to be implemented in an extensive P-T range using up-to-date methods.  相似文献   

3.
Thermal diffusivity (D) was measured using laser-flash analysis on pristine and remelted obsidian samples from Mono Craters, California. These high-silica rhyolites contain between 0.013 and 1.10?wt% H2O and 0 to 2?vol% crystallites. At room temperature, D glass varies from 0.63 to 0.68?mm2?s?1, with more crystalline samples having higher D. As T increases, D glass decreases, approaching a constant value of ??0.55?mm2?s?1 near 700?K. The glass data are fit with a simple model as an exponential function of temperature and a linear function of crystallinity. Dissolved water contents up to 1.1?wt% have no statistically significant effect on the thermal diffusivity of the glass. Upon crossing the glass transition, D decreases rapidly near ??1,000?K for the hydrous melts and ??1,200?K for anhydrous melts. Rhyolitic melts have a D melt of ??0.51?mm2?s?1. Thermal conductivity (k?=?D·??·C P) of rhyolitic glass and melt increases slightly with T because heat capacity (C P) increases with T more strongly than density (??) and D decrease. The thermal conductivity of rhyolitic melts is ??1.5?W?m?1?K?1, and should vary little over the likely range of magmatic temperatures and water contents. These values of D and k are similar to those of major crustal rock types and granitic protoliths at magmatic temperatures, suggesting that changes in thermal properties accompanying partial melting of the crust should be relatively minor. Numerical models of shallow rhyolite intrusions indicate that the key difference in thermal history between bodies that quench to obsidian, and those that crystallize, results from the release of latent heat of crystallization. Latent heat release enables bodies that crystallize to remain at high temperatures for much longer times and cool more slowly than glassy bodies. The time to solidification is similar in both cases, however, because solidification requires cooling through the glass transition in the first case, and cooling only to the solidus in the second.  相似文献   

4.
The groundwater of the Korba plain represents major water resources in Tunisia. The Plio‐Quaternary unconfined aquifer of the Cap‐Bon (north‐east Tunisia) is subject to the intensive agricultural activities and high groundwater pumping rates due to the increasing of the groundwater extraction. The degradation of the groundwater quality is characterized by the salinization phenomena. Groundwater were sampled and analysed for physic‐chemical parameters: Ca2+, Mg2+, Na+, K+, Cl‐, SO42‐, HCO3‐, NO3‐, pH, electrical conductivity (EC), and the temperature (T°). The hydrochemical analysis is coupled with the calculation of the saturation indexes (SI gypsum, SI halite, SI calcite and SI dolomite), ionic derivation and with the ion correlations compared to chloride concentrations: Na+/ Cl‐, Ca2+/ Cl‐ and Mg2+/ Cl‐ ratios. Seawater fractions in the groundwater were calculated using the chloride concentration. Those processes can be used as indicators of seawater intrusion progression. EC methods were also conducted to obtain new informations on the spatial scales and dynamics of the fresh water–seawater interface of coastal groundwater exchange. The mixing zone between freshwater and saltwater was clearly observed from the EC profile in the investigated area where a strong increase in EC with depth was observed, corresponding to the freshwater and saltwater interface. Results of hydrochemical study revealed the presence of direct cation exchange linked to seawater intrusion and dissolution processes associated with cations exchange. These results, together with EC investigation, indicated that the groundwater is affected by seawater intrusion and is still major actor as a source of salinization of the groundwater in Korba coastal plain. Further isotopic and hydrological investigations will be necessary to identify and more understood the underlying mechanisms. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

5.
High-temperature experiments on ferromagnesian compositions have been hampered by the rapid absorption of up to 95% of the original iron by platinum and 40% by silver-palladium capsules. Molybdenum or iron capsule materials can decrease or alleviate iron loss, but restrict oxygen fugacities to values near the iron-wustite buffer. Because Co2+ is stable at fO2 =HM and because the solubility of Co in platinum in this range of fO2 is ～0.05% at temperatures to 1350°C, its use as an analogue for Fe2+ is possible. In addition, experiments simulating various Fe2+ ratios can be easily performed by choosing appropriate Co2+/Fe3+ ratios. The cobalt phases produced possess brilliant and distinctive colors which are valuable aids in optical identification of minute phases. The cobalt analogue hypothesis was tested with atmospheric pressure experiments in air on the cobalt analogue of the 1921 Kilauea basalt at three simulated Fe2+/Fe3+ ratios. The results were compared with those of R.E.T. Hill (1969) for the natural 1921 basalt. The phase relations were the same, with the cobalt system stability fields systematically shifted by about +50°C. Microprobe analysis of olivines and the coexisting glasses indicate that the distribution of Co2+ between olivine and melt is independent of temperature and liquid composition. Although the analogue liquid composition differs from the equilibrium composition of the natural system, it may be corrected be employing distribution coefficients (KD = 0.61 for the Co system; KD = 0.33 for the Fe system) to closely approximate what the natural system would yield if iron loss did not occur.  相似文献   

6.
The electrical conductivity of a single crystal of San Carlos olivine (Fo92, 0.16 wt.% Fe2O3) has been measured as a function of temperature and oxygen fugacity (fO2). After heating to 1338°C at fO2 = 10?12 atm., the conductivity at 950°C was 10?5 (ohm-m)?1, almost 3 orders of magnitude less than that measured in air. This decrease is due to the reduction of Fe3+ to Fe2+. Further heating to 1500°C at fO2 = 10?14 atm., decreased the electrical conductivity at 950°C to 10?6 (ohm-m)?1. When recovered at room temperature, the speciment had Fo96 composition and contained small, opaque blebs distributed throughout the crystal. Derivations of temperature profiles for the earth's mantle from conductivity-depth models must take account of the important role played by iron oxidation state in the electrical conductivity of olivine.  相似文献   

7.
The relative rate constants of O2(b1Σ g + , v= 1–4) production at an inelastic interaction between electronically excited N(2D) atoms and O2(X3Σ g ? , v = 0) oxygen molecules have been calculated. It was shown that an increase in equilibrium distances between oxygen atoms in NO2 quasi-molecule, produced during the interaction, substantially increases the calculated relative production rates of O2(b1Σ g + , v > 1). The obtained coefficients are used to calculate the O2(b1Σ g + , v= 1–4) relative populations at 110 km (T = 250 K) and 150 km (T = 500 K) altitudes of the polar ionosphere. The calculated populations have been compared with the results of the published measurements of the Atmospheric system band luminosity intensities, and satisfactory agreement has been obtained for low altitudes.  相似文献   

8.
The temperature dependence of water diffusivity in rhyolite melts over the range 650–950°C and [PT(H2O] = 700 bars is evaluated from water concentration-distance profiles measured in glass with an ion microprobe. Diffusivities are exponentially dependent on concentration over this temperature range and vary from about 10?8 cm2/s at 650°C to about 10?7 cm2/s at 950°C at 2 wt.% water. Water solubility also varies with temperature at a rate of ?0.14 wt. per 100°C increase. The avtivation energy (Ea) appears to be constant at 19 ± 1kal/mole for 1, 2,and 3 wt.% H2O. Comparison of these data with results for cation diffusion indicates that this value is a minimum Ea for diffusion of any species in a rhyolite melt.Compensation plots of log10D0 (the frequency factor) versus Ea indicate that hydrous rhyolite melts follow the same trend as anhydrous basalts. D0 increases for H2O and Ca2+ [1] as Ea decreases. This suggests that these molecules may diffuse by different mechanisms than do monovalent cations, and that hydration of the melt affects diffusion of Ca2+ and H2O differently than it does monovalent cation diffusion. The results imply that dramatic increases in cation diffusivities by hydration [1] may occur with additions of less than 1 wt.% H2O.  相似文献   

9.
A hierarchical sampling programme (including continuous monitoring, twice-daily sampling and sampling at hourly intervals over selected 24 hour periods) was devised to support hydrochemical and hydrological research programmes on an alpine proglacial stream. The rationale for the research and for the sampling programme are explained and the hydrochemical time series generated over an ablation season are analysed to assess the degree to which they support the study aims. It appears that there is no satisfactory substitute for the chemical analysis of at least two water samples taken at approximately maximum and minimum discharge every day, if seasonal variations in meltwater chemistry are to be effectively characterized. Such time series data can be used to estimate Box-Jenkins transfer function-noise models between particular solutes (SO2−4, Ca2+, Mg2+, Na+ and possibly K+) and either discharge or electrical conductivity, which can then be used to fill any short gaps in the data. This approach is not satisfactory even for filling short gaps in the twice-daily determinations of pH, HCO−3 and NO−3. At the diurnal time-scale (based on hourly determinations over 24 hour periods) electrical conductivity seems to provide a good surrogate for most of the solutes studied. HCO−3, SO2−4, Ca2+ and Mg2+ were found to be particularly strongly related to electrical conductivity and there was little if any significant serial autocorrelation in the residuals from all of the simple linear regression relationships that were estimated between individual species and conductivity. It is concluded that the hierarchical sampling design was suitable for the purposes of the study, and that the continuous monitoring of electrical conductivity provides excellent supporting information to the chemical analysis of water samples if it is used carefully as a means of short term calibration and interpolation of the solute record.  相似文献   

10.
Hydrothermal experiments in the temperature range 750–1020°C have defined the saturation behavior of zircon in crustal anatectic melts as a function of both temperature and composition. The results provide a model of zircon solubility given by: In DZrzircon/melt= ?3.80?[0.85(M?1)]+12900/T where DZrzircon/melt is the concentration ratio of Zr in the stoichiometric zircon to that in the melt, T is the absolute temperature, and M is the cation ratio (Na + K + 2Ca)/(Al · Si). This solubility model is based principally upon experiments at 860°, 930°, and 1020°C, but has also been confirmed at temperatures up to 1500°C for M = 1.3. The lowest temperature experiments (750° and 800°C) yielded relatively imprecise, low solubilities, but the measured values (with assigned errors) are nevertheless in agreement with the predictions of the model.For M = 1.3 (a normal peraluminous granite), these results predict zircon solubilities ranging from ～ 100 ppm dissolved Zr at 750°C to 1330 ppm at 1020°C. Thus, in view of the substantial range of bulk Zr concentrations observed in crustal granitoids (～ 50–350 ppm), it is clear that anatectic magmas can show contrasting behavior toward zircon in the source rock. Those melts containing insufficient Zr for saturation in zircon during melting can have achieved that condition only by consuming all zircon in the source. On the other hand, melts with higher Zr contents (appropriate to saturation in zircon) must be regarded as incapable of dissolving additional zircon, whether it be located in the residual rocks or as crystals entrained in the departing melt fraction. This latter possibility is particularly interesting, inasmuch as the inability of a melt to consume zircon means that critical geochemical “indicators” contained in the undissolved zircon (e.g. heavy rare earths, Hf, U, Th, and radiogenic Pb) can equilibrate with the contacting melt only by solid-state diffusion, which may be slow relative to the time scale of the melting event.  相似文献   

11.
Groundwater quality in Ma’an area was evaluated for its suitability for drinking and agricultural uses by determining the main physical and chemical properties during a 1 year survey study (August 2009 to August 2010). Several samples were collected from ten different wells and analysed for temperature, pH, conductivity, total dissolved solids, total hardness, major cations (Ca2+, Mg2+, Na+ and K+), major anions (HCO3 ?, Cl?, NO3 ?, SO4 2?, F? and Br?) and trace metals (Fe2+, Al3+, Mn2+, Cu2+, Zn2+, Pb2+ and Cd2+). The general chemistry of water samples was typically of alkaline earth waters with prevailing bicarbonate chloride. The results showed great variations among the analyzed samples with respect to their physical and chemical parameters. However, most values were below the maximum permissible levels recommended by Jordanian and WHO drinking water standards. The quality assessment shows that in general, the GW in the study area is not entirely fit for direct drinking with respect to EC, and Pb2+. According to the residual sodium carbonate and sodium adsorption ratio, the water in the studied wells can be used for irrigational purposes.  相似文献   

12.
Sixteen sets of apatite/liquid partition coefficients (Dap/liq) for the rare earth elements (REE; La, Sm, Dy, Lu) and six values for Sr were experimentally determined in natural systems ranging from basanite to granite. The apatite + melt (glass) assemblages were obtained from starting glasses artificially enriched in REE, Sr and fluorapatite components; these were run under dry and hydrous conditions of 7.5–20 kbar and 950–1120°C in a solid-media, piston-cylinder apparatus. An SEM-equipped electron microprobe was used for subsequent measurement of REE and Sr concentrations in coexisting apatites and quenched glasses. The resulting partition coefficient patterns resemble previously determined apatite phenocryst/groundmass concentration ratios in the following respects: (1) the rare earth patterns are uniformly concave downward (i.e., the middle REE are more compatible in apatite than the light and heavy REE); (2) DREEap/liq is much higher for silicic melts than for basic ones; and (3) strontium (and therefore Eu2+) is less concentrated by apatite than are the trivalent REE. The effects of both temperature and melt composition on DREEap/liq are systematic and pronounced. At 950°C, for example, a change in melt SiO2 content from 50 to 68 wt.% causes the average REE partition coefficient to increase from ～7 to ～30. A 130°C increase in temperature, on the other hand, results in a two-fold decrease in DREEap/liq. Partitioning of Sr is insenstitive to changes in melt composition and temperature, and neither the Sr nor the REE partition coefficients appear to be affected by variations in pressure or H2O content of the melt.The experimentally determined partition coefficients can be used not only in trace element modelling, but also to distinguish apatite phenocrysts from xenocrysts in rocks. Reported apatite megacryst/host basalt REE concentration ratios [12], for example, are considerably higher than the equilibrium partition coefficients, which suggest that in this particular case the apatite is actually xenocrystic.A reversal experiment incorporated in our study yielded diffusion profiles of REE in apatite, from which we extracted a REEαCa interdiffusion coefficient of 2–4×10?14 cm2/s at 1120°C. Extrapolated downward to crustal temperatures, this low value suggests that complete REE equilibrium between felsic partial melts and residual apatite is rarely established.  相似文献   

13.
Iwojima volcano, located on the southernmost part of the Izu-Ogasawara arc, is characterized by the extrusion of trachyte or trachy andesite lavas and pyroclastic rocks of Holocene and surface thermal manifestations. Small phreatic explosions have been recorded frequently during the last 100 years with the most recent in 1999 and 2001. In order to elucidate the behavior of volcanic volatiles and to assess the potential activity of this volcano, diffuse CO2 efflux, CO2 content and δ13C–CO2 in soil gas, and soil temperature at 30 cm depth were measured at 272 sites in March 2000, 112 sites in December 2000 and 40 sites in December 2001. We found that high CO2 efflux values, of more than 100 g m−2 day−1, occurred at several locations on Motoyama volcano corresponding with high soil temperatures (more than 60 °C at 30 cm depth) region and with areas where CO2 with magmatic δ13C was observed. Here, the magmatic δ13C determined for fumarolic CO2 data ranged from −2‰ to +3‰, which is clearly higher than magmatic gas values (−8‰ to −2‰) typically found in island arc settings around the world. However, this can be explained in terms of carbon-isotope fractionation between calcite and CO2 under subsurface temperature and pressure conditions at Iwojima. A total efflux of CO2 for Iwojima volcano is estimated to be 760 t day−1, with a magmatic contribution of about 450 t day−1. This value is rather high compared with other volcanoes in island arc settings. Since Iwojima has no visible plume, almost all volcanic CO2 is released as diffuse efflux through the volcanic edifice.  相似文献   

14.
The electrical impedance of a sintered forsterite sample containing 1 mol percent SiO2 in excess has been studied as a function of frequency (1–105 Hz) and temperature (400–900°C). The electrical properties are strongly frequency-dependent, requiring both conduction and displacement current for their interpretation. The electrical conductivity is thermally activated with a mean activation energy of 1.15 eV. It is interpreted as being ionic and caused by migration of magnesium ions via a vacancy mechanism. Dielectric data deduced from impedance measurements vary as ωn?1 (0 < n < 1) at constant temperature. The value of n is different below and above a critical frequency ωc, which is thermally activated and interpreted as the jump frequency of the migrating species.  相似文献   

15.
The main properties of conducting zones in the lithosphere are examined. They are compared with data of the gravitational field, seismology, seismic tomography, and some other geological and geophysical studies. The possible origin of the conducting zones is considered. Their high conductivity is connected with the presence of mineralized solutions and magmatic melts. A rough estimate is given for the concentration of mineralized solutions in these zones. Regions of conducting zones correlating with anomalies of lower P wave velocities are associated with the presence of magmatic melts. An approximate estimate is obtained for the concentration of magmatic melts in the lithospheric zone beneath the Klyuchevskaya group of volcanoes.  相似文献   

16.
The chemical and isotopic compositions (δDH2O, δ18OH2O, δ18OCO2, δ13CCO2, δ34S, and He/N2 and He/Ar ratios) of fumarolic gases from Nisyros, Greece, indicate that both arc-type magmatic water and local seawater feed the hydrothermal system. Isotopic composition of the deep fluid is estimated to be +4.9±0.5‰ for δ18O and ?11±5‰ for δD corresponding to a magmatic water fraction of 0.7. Interpretation of the stable water isotopes was based on liquid–vapor separation conditions obtained through gas geothermometry. The H2–Ar, H2–N2, and H2–H2O geothermometers suggest reservoir temperatures of 345±15 °C, in agreement with temperatures measured in deep geothermal wells, whereas a vapor/liquid separation temperature of 260±30 °C is indicated by gas equilibria in the H2O–H2–CO2–CO–CH4 system. The largest magmatic inputs seem to occur below the Stephanos–Polybotes Micros crater, whereas the marginal fumarolic areas of Phlegeton–Polybotes Megalos craters receive a smaller contribution of magmatic gases.  相似文献   

17.
Revealing of the sources and distributions of sedimentary organic matter in the East China Sea (ECS) is important for understanding its carbon cycle, which has significant temporal and spatial variability due to the influences of recent climate changes and anthropogenic activities. In this study, we report the contents of both terrestrial and marine biomarkers including ∑C27+C29+C31n-alkanes (38.6-580 ng/g), C37 alkenones (5.6-124.6 ng/g), brassicasterol (98-913 ng/g) and dinosterol (125-1521 ng/g) from the surface sediments in the Changjiang River Estuary (CRE) and shelf areas of the ECS. Several indices based on biomarker contents and ratios are calculated to assess the spatial distributions of both terrestrial and marine organic matter in the ECS surface sediments, and these results are compared with organic matter distribution patterns revealed by the δ13C (−20.1‰ to −22.7‰) and C/N ratio (5-7.5) of total organic matter. The contents of terrestrial biomarkers in the ECS surface sediments decrease seaward, controlled mostly by Changjiang River (CR) inputs and surface currents; while higher contents of the two marine biomarkers (brassicasterol and dinosterol) occur in upwelling areas outside the CRE and in the Zhejiang-Fujian coastal zone, controlled mostly by marine productivity. Four proxies, fTerr(δ13C) (the fraction of terrestrial organic matter in TOC estimated by TOC δ13C), odd-alkanes (∑C27+C29+C31n-alkanes), 1/Pmar-aq ((C23+C25+C29+C31)/(C23+C25) n-alkanes) and TMBR (terrestrial and marine biomarker ratio) (C27+C29+C31n-alkanes)/((C27+C29+C31) n-alkanes+(brassicasterol+dinosterol+alkenones)), reveal a consistent pattern showing the relative contribution of terrestrial organic matter (TOM) is higher in the CRE and along the Zhejiang-Fujian coastline, controlled mostly by CR inputs and currents, but the TOM contribution decreases seaward, as the influences of the CR discharge decrease.  相似文献   

18.
We investigated the concentration and site occupation of ferric iron (Fe3+) in (Mg,Fe)O to understand the influence of point defects on transport properties such as atomic diffusion, electrical conductivity and viscosity. We conducted Mössbauer spectroscopy of (Mg0.8Fe0.2)O single crystals synthesized at temperatures from 1673 to 2273 K and pressures from 5 to 15 GPa with Re–ReO2 and Mo–MoO2 oxygen fugacity buffers. The isomer shift of the Mössbauer spectra suggests that Fe3+ occupies mostly the tetrahedral site at reduced conditions and both the octahedral and tetrahedral sites at oxidized conditions. We formulate a thermodynamic model of point defect dissolution in (Mg,Fe)O which suggests that unassociated tetrahedral Fe3+ is more stable than unassociated octahedral Fe3+ at high-pressure and low oxygen fugacity due to the effect of configurational entropy. The pressure dependence of Fe3+ concentration indicates a change in the dominant site occupancy of Fe3+: (1) Fe3+ in the tetrahedral site, (2) Fe3+ in the octahedral site, and (3) defect clusters of Fe3+ and cation vacancy, in the order of increasing oxygen fugacity and decreasing pressure. This is in reasonable agreement with previously reported experiments on Fe3+ concentration, Mg–Fe interdiffusivity and electrical conductivity. We consider it plausible that (Mg,Fe)O accommodates Fe3+ in the tetrahedral site down to the lower mantle. Based on our results and available experimental data, we discuss the solubility competition between Fe3+ and protons (H+), and its implications for transport properties in the lower mantle.  相似文献   

19.
The viscosity of natural rhyolitic melt from Lipari, Aeolian Islands and melt-bubble emulsions (30–50 vol% porosity) generated from Lipari rhyolite have been measured in a concentric cylinder rheometer at temperatures and shear rates in the range 925–1150°C and 10−3–10−1.2 s−1, respectively, in order to better understand the dependence of emulsion shear viscosity on temperature and shear rate in natural systems. Bubble-free melt exhibits Newtonian–Arrhenian behavior in the temperature range 950–1150°C with an activation energy of 395±30 kJ/mol; the shear viscosity is given by log ηm=−8.320+20624/T. Suspensions were prepared from natural rhyolite glass to which small amounts of Na2SO4 were added as a ‘foaming agent’. Reasonably homogeneous magmatic mixtures with an approximate log-normal distribution of bubbles were generated by this technique. Suspension viscosity varied from 106.1 to 108.37 Pa s and systematically correlates with temperature and porosity in the shear stress range (104.26–105.46 Pa) of the experiments. The viscosity of melt-bubble emulsions is described in terms of the relative viscosity, ηr=ηe/ηm where ηe is the emulsion viscosity and ηm is the viscosity of melt of the same composition and temperature. The dependence of relative viscosity on porosity for magmatic emulsions depends on the magnitude of the capillary number Ca≡G/(σrb−1ηm−1), the ratio of viscous forces acting to deform bubbles to interfacial forces resisting bubble deformation. For inviscid bubbles in magmatic flows three regimes may be identified. For Ca<0.1, bubbles are nearly spherical and relative viscosity is an increasing function of porosity. For dilute systems, ηr=1+φ given by the classical result of Taylor [Proc. R. Soc. London A 138 (1932) 41–48]. For Ca in the range 0.1<Ca<10, emulsions behave as power law fluids and the relative viscosity depends on shear rate (or Ca) as well as porosity. At high Ca (Ca>10) an asymptotic regime is reached in which relative viscosity decreases with increasing porosity and is independent of Ca. Our experiments were carried out for 30<Ca<925 in order to quantify the maximal effect of bubbles in reducing the viscosity of magmatic emulsions relative to single-phase melt at identical conditions of shear rate and temperature. The viscosity of a 50 vol% emulsion is a factor of five smaller than that of melt alone. Rheometric measurements obtained in this study are useful in constraining models of magma transport and volcanic eruption mechanics relevant to transport of volatile-saturated magma in the crust and upper mantle.  相似文献   

20.
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