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1.
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   

2.
Tracer diffusion coefficients for Li in glasses of albite, orthoclase, and obsidian composition have been determined by a method involving deposition of a thin source on polished glass wafers, anneal under controlled temperature conditions (300–900°C), and ion-microprobe determination of the concentration profile. All results conform to an Arrhenius-type relationship,D = D0exp(?Q/RT), whereQ is 23, 17, and 22 kcal mol?1;D0 is 0.2, 0.003, and 0.03 cm2s?1 for albite and orthoclase glasses, and obsidian respectively. Lithium is thus a fast diffusing ion and behaves similarly to sodium in the same glasses. A mechanism involving jumps of the diffusing ions through oxygen hexagonal rings is suggested by consideration of ionic radii ratio of alkali (H, Li, Na, K, Rb, and Cs) ions to the oxygen anions.  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.
A semiempirical mathematical model of iron and manganese migration from bottom sediments into the water mass of water bodies has been proposed based on some basic regularities in the geochemistry of those elements. The entry of dissolved forms of iron and manganese under aeration conditions is assumed negligible. When dissolved-oxygen concentration is <0.5 mg/L, the elements start releasing from bottom sediments, their release rate reaching its maximum under anoxic conditions. The fluxes of dissolved iron and manganese (Me) from bottom sediments into the water mass (J Me) are governed by the gradients of their concentrations in diffusion water sublayer adjacent to sediment surface and having an average thickness of h = 0.025 cm: \({J_{Me}} = - {D_{Me}}\frac{{{C_{Me\left( {ss} \right)}} - {C_{Me\left( w \right)}}}}{h}\) (D Me ≈ 1 × 10–9 m2/s is molecular diffusion coefficient of component Me in solution; C Me(ss) and C Me(w) ≈ 0 are Me concentrations on sediment surface, i.e., on the bottom boundary of the diffusion water sublayer, and in the water mass, i.e., on the upper boundary of the diffusion water sublayer). The value of depends on water saturation with dissolved oxygen (\({\eta _{{O_2}}}\)) in accordance with the empiric relationship \({C_{Me\left( {ss} \right)}} = \frac{{C_{_{Me\left( {ss} \right)}}^{\max }}}{{1 + k{\eta _{{O_2}}}}}\) (k is a constant factor equal to 300 for iron and 100 for manganese; C Me(ss) max is the maximal concentration of Me on the bottom boundary of the diffusion water sublayer with C Fe(ss) max ≈ 200 μM (11 mg/L), and C Mn(ss) max ≈ 100 μM (5.5 mg/L).  相似文献   

5.
Hudson River sediment microcosms from Piles Creek (PC), Piermont Marsh (PM), and Iona Island (II) were amended with ∼100 mM nitrate or sulfate to stimulate anaerobic bioremediation. Nitrate and sulfate decreased over two years of field incubation and the fraction of these losses due to diffusion to the water column was predicted using Fick’s law. Apparent diffusion (Dapp) values of 1-4 × 10−10 m2 s−1 predicted the majority of loss/gain from/to the sediments by 700 d, but not at all times. Effective diffusion (Deff) values predicted by the porosity function (Deff = Dmol ε4/3) were larger than those observed in the field, and field data indicates a cube power relationship: Deff = Dmol ε3. Dapp greatly increased in surficial layers at PM and PC in year two, suggesting that bioadvection caused by bioturbating organisms had occurred. The effects of bioturbation on transport to/from the sediments are modeled, and results can be applied to various sediment treatment scenarios such as capping.  相似文献   

6.
The content of K, Th and U in the continental crust is estimated based on the assumption that the concentration of these elements decreases with depth asAx = A0e?x/D [11], withAx andA0 the heat production rates at depthx and at the surface, respectively. Taking the weighted mean heat production rate of the intrusive rocks of the upper crust asA0 = 2.33 μWm?3, that of the granulites representing the lower crust asAx = 0.72 μWm?3, and the mean scale heightD= 9.5km [1] the average vertical distancex = b between these intrusives and granulites is 11.2 km. Withb known and the average concentrations of K, Th and U in granulites and intrusive rocks of the upper crust the scale heights of the vertical distribution of these elements areDK = 71km,DTh = 9.5km,DU = 5.8km. The knowledge of these parameters permits to calculate the average concentrations of these elements in a 33.3 km thick crust:K= 2.19%,Th= 4.43ppm,U= 0.66ppm; Th/U = 6.7 and K/U = 3.3 × 104. The resulting heat flow is 23.0 mW m?2 which is practically identical with the value deduced from heat flow measurements. Assuming that the Th/U ratio of the entire crust—including the sediments—is 3.9, the high ratio of 6.7 in the crystalline crust indicates that about 7.2 × 1012 t U were extracted from it. All rocks with Th/U ratios <3.9 are possible sinks of this U. About half that amount is deposited in sedimentary rocks, mainly in black shales. The second important sink are the volcanic rocks of the continental margins.  相似文献   

7.
Tidal current and elevation data were collected from five oceanographic moorings during October 2004 in Torres Strait, northern Australia, to assess the effects of large bedforms (i.e., sand banks) on the drag coefficient (CD) used for estimating bed shear stress in complex shallow shelf environments. Ten minute averages of tidal current speed and elevation data were collected for 18 days at an on-bank site (<7 m water depth) and an off-bank site (<10 m). These data were compared to data collected simultaneously from two shelf locations (<11 m) occupied to measure regional tidal behaviour. Overall CD estimates at the on- and off-bank sites attained 7.0±0.1×10−3 and 6.6±0.1×10−3, respectively. On-bank CD estimates also differed between the predominant east–west tidal streams, with easterly directed flows experiencing CD=7.8±0.18×10−3 and westerly directed flows CD=6.4±0.12×10−3. Statistically significant differences between the off-bank and on-bank sites are attributed to the large form drag exerted by the sand banks on the regional tidal currents, and statistically significant differences between the westward and eastward flows is ascribed to bedform asymmetry. Form drag from the large bedforms in Torres Strait comprises up to 65% of the total drag coefficient. When constructing sediment transport models, different CD estimates must therefore be applied to shelf regions containing steep bedforms compared to regions that do not. Our results extend the limited inventory of seabed drag coefficients for shallow shelf environments, and can be used to improve existing regional seabed mobilisation models, which have direct application to environmental management in Torres Strait.  相似文献   

8.
Abstract

Abstract Recently, substantial progress has been made in detection and observation of non-aqueous phase liquids (NAPLs) in the subsurface using different experimental techniques. However, there is still a lack of appropriate direct methods to measure the saturation of NAPL (θNAPL). This paper provides a guide for estimating θNAPL and water content (θ w ) in unsaturated and saturated sand based on direct measurements of soil dielectric constant (Ka ) and electrical conductivity (σ a ) using time domain reflectometry (TDR). The results show that the previously used dielectric mixing model fails to predict θNAPL in the case of a four-phase system. A new methodology is suggested and exemplified by showing that the measured Ka gives accurate estimation of θNAPL for a three-phase system while in a four-phase system, both θ a and Ka need to be measured. The results show that using the suggested methodology, accurate predictions of θ w (R 2 = 0.9998) and θNAPL lower than 0.20 m3 m-3 (average R 2 = 0.9756) are possible.  相似文献   

9.
Fe-Mg interdiffusivities in (Fe,Mg)O magnesiowüstite have been measured in experiments conducted at pressures of 7-35 GPa and temperatures of 1573-1973 K using a Kawai-type high-pressure apparatus. The diffusion profiles were measured across the interface between MgO and (Fe0.5,Mg0.5)O samples by electron microprobe analysis, and the Fe-Mg interdiffusivities were determined as DFe-Mg=D0exp{−E*(1+PV*Mg/E*Mg)/RT}, where D0=4.1(+16.1−3.3)×10−7 m2/s, E*=(1−CMg)E*Fe+CMgE*Mg (activation energy for the concentration of Mg, where E*Fe=113(±74) kJ/mol and E*Mg=226(±32) kJ/mol), the activation volume V*Mg=1.8(±1.2)×10−6 m3/mol. By extrapolating these results to the P-T conditions of the core-mantle boundary, we conclude that the interdiffusivity of Fe-Mg in magnesiowüstite at the bottom of the lower mantle is at least one order of magnitude larger than that at the top of the lower mantle.  相似文献   

10.
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   

11.
Absolute18O content of standard mean ocean water   总被引：1，自引：0，他引：1  
The absolute values of the18O/16O ratio (Rs) and the relative18O content (Xs) in SMOW have been determined by comparing SMOW mass spectrometrically with well-defined synthetic mixtures of pure D218O and H216O. The results are:RS = (2005.20 ± 0.45) × 10?6, XS = (2000.45 ± 0.45) × 10?6  相似文献   

12.
In this paper, we discussed the influence of the initial tectonic stress on the relative measurement value of the ground stress when a long cylindrical straingauge is used in the viscoelastic media. We simulate the whole system consisting of the stratum, cement ring and the straingauge cylinder with a three-layer-medium model and obtain the solution of radial displacement on the inner wall of the straingauge under the action of initial tectonic stress by using the correspondence principle. The result showes: 1) The influence of initial stress making of the radial displacement on the inner wall of the straingauge increases gradually with time at a gradually reduced rate and tends to a certain value eventually; 2) The principal stress with a magnitude of [C 0+C 1 exp (?ω 1t)+C 2 exp (?w 2 t]σ 10 in the opposite direction of initial stress will be superimposed to the measuring result of stress change without considering the initial stress. whereC 0,C 1,C 2 andω 1,ω 2 are related only to the mechanical property of the stratum,σ i0 (i=1, 2) are the two principal components of the initial tectonic stress. It is pointed out that the initial tectonic stress affects obviously on the measurement of the relative change of ground stress in the cases of soft strata and high initial stress.  相似文献   

13.
The complexity of the relationships between Alexandrium minutum (A.m.) concentration in the water ([A.m.]w), Paralytic Shellfish Poisoning contamination in the digestive gland ([PSP]dg) and valve behavior was explored in oysters Crassostrea gigas. Two experiments were conducted, during which oysters’ valve behaviour were analyzed. Oysters, first acclimated for 10-days with the non harmful microalgae Heterocapsa triquetra (H.t.), were exposed to four microalgae mixtures at constant total concentrations of 10 × 103 cells ml−1 (experiment-1) and 5 × 103 cells ml−1 (experiment-2): 100% A.m.; 50% A.m.-50% H.t.; 25% A.m.-75% H.t.; 100% H.t. At the end of experiment-2, [PSP]dg were measured.At 10 × 103 cells ml−1, the microalgal ingestion decreased (p < 0.05) with increasing [A.m.]w but not at 5 × 103 cells ml−1 (p > 0.05). The frequency of microclosures specifically increased with [A.m.]w (p < 0.05) and the opening duration with [PSP]dg (p < 0.0001). Oysters exhibiting the maximum increase in opening duration also exhibited the highest [PSP]dg. The results are discussed in terms of oyster physiology and origin of the behavioral response.  相似文献   

14.
Partitioning resistance to overland flow on rough mobile beds   总被引：1，自引：0，他引：1  
For overland flows transporting predominantly bed load over rough mobile beds without rainfall, resistance to flow f may be divided into four components: surface resistance fs, form resistance ff, wave resistance fw, and bed‐mobility resistance fm. In this study it is assumed that f = fs + ff + fw + fm, and an equation is developed for each component. The equations for fs and ff are borrowed from the literature, while those for fw and fm are developed from two series of flume experiments in which the beds are covered with various concentrations of large‐scale roughness elements. The first series consists of 65 experiments on fixed beds, while the second series contains 194 experiments on mobile beds. All experiments were performed on the same slope (S = 0·114) and with the same size of sediment (D = 0·00074 m). The equations for fw and fm are derived by a combination of dimensional analysis and regression analysis. The analyses reveal that the major controls of fw and fm are the Froude number F and the concentration of the roughness elements Cr. When the equations for fw and fm are summed, the Cr terms cancel out, leaving fw+m = 0·63F?2. An equation is developed that predicts total f, and the contributions of fs, ff, fw and fm to f are computed from the series 1 and 2 experiments. An analysis of the first series reveals that in clear‐water flows over fixed beds, fw accounts for 52 per cent of f. A similar analysis of the second series indicates that in sediment‐laden flows over mobile beds fw comprises 37 per cent and fm 32 per cent of f, so that together fw and fm account for almost 70 per cent of f. Finally, regression analyses indicate that where F > 0·5, fw and fm each vary with F?2 and fw/fm = 1·18. The equation developed here for predicting total f applies only to the range of hydraulic, sediment, and bed roughness conditions represented by the experimental data. With additional data from a broader range of conditions the same methodology as employed here could be used to develop a more general equation. Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   

15.
Three physical quantities define the essentials of the cosmic ray exposure history of a sample of an iron meteorite: (1) the cosmic ray exposure age T, (2) the pre-atmospheric “size” S of the irradiated body, and (3) the location, i.e. the “depth” D, of the samples within the body. To establish these quantities for a given sample three independent quantities must be determined experimentally. In the present work T is ascertained by the 41K/40K method and the 4He and 21Ne concentrations (C4 and C21) are measured by the isotope dilution method. Signer and Nier's evaluation of the rare gas distribution in the meteorite Grant and the measured exposure age for this meteorite provide the relationships allowing to ascertain for any meteorite the quantities S and D from the 21Ne production rate (P21 = C21/T) and the 4He/21Ne ratio.Earlier measurements have provided data on the isotopic composition of potassium in 74 different iron meteorites. New rare gas measurements are reported for some 40 samples. Results on the age, size and depth are obtained for almost 60 samples. These data suggest that Signer and Nier's model is well suited for describing not only the rare gas distribution in a single selected meteorite (Grant) but also the exposure histories of the great majority of all irons. For a few samples, however, secondary breakups of the meteoroid and a two- or multiple-stage irradiation must be invoked. Further measurements are proposed for testing and, possibly, refining the still somewhat uncertain relationships between the abundances of cosmogenic nuclides and the quantities T, S, and D in very large meteorites.Histograms are presented showing the age distributions for irons of different chemical groups and of different size ranges.The feasibility and the relative merits of other methods for the determination of T, S, and D are discussed.  相似文献   

16.
The quality of earthquake prediction is usually characterized by a two-dimensional diagram n versus τ, where n is the rate of failures-to-predict and τ is a characteristic of space–time alarm. Unlike the time prediction case, the quantity τ is not defined uniquely. We start from the case in which τ is a vector with components related to the local alarm times and find a simple structure of the space–time diagram in terms of local time diagrams. This key result is used to analyze the usual 2-d error sets {n, τ w } in which τ w is a weighted mean of the τ components and w is the weight vector. We suggest a simple algorithm to find the (n, τ w ) representation of all random guess strategies, the set D, and prove that there exists the unique case of w when D degenerates to the diagonal n + τ w  = 1. We find also a confidence zone of D on the (n, τ w ) plane when the local target rates are known roughly. These facts are important for correct interpretation of (n, τ w ) diagrams when we discuss the prediction capability of the data or prediction methods.  相似文献   

17.
The water retention curve (θ(ψ)), which defines the relationship between soil volumetric water content (θ) and matric potential (ψ), is of paramount importance in characterizing the hydraulic behaviour of soils. However, few methods are so far available for estimating θ(ψ) in undisturbed soil samples. We present a new design of TDR‐pressure cell (TDR‐Cell) for estimating θ(ψ) in undisturbed soil samples. The TDR‐Cell consists of a 50‐mm‐long and 50‐mm internal diameter stainless steel cylinder (which constitutes the outer frame of a coaxial line) attached to a porous ceramic disc and closed at the ends with two aluminium lids. A 49‐mm‐long and 3‐mm‐diameter stainless steel rod, which runs longitudinally through the centre of the cylinder, constitutes the inner rod of a coaxial TDR probe. The TDR‐Cell was used to determine the θ(ψ) curves of a packed sand and seven undisturbed soil samples from three profiles of agricultural soils. These θ(ψ) curves were subsequently compared to those obtained from the corresponding 2‐mm sieved soils using the pressure plate method. Measurements of bulk electrical conductivity, σa, as a function of the water content, σa(θ), of the undisturbed soil samples were also performed. An excellent correlation (R2 = 0·988) was found between the θ values measured by TDR on the different undisturbed soils and the corresponding θ obtained from the soil gravimetric water content. A typical bimodal θ(ψ) function was found for most of the undisturbed soil samples. Comparison between the θ(ψ) curves measured with the TDR‐Cell and those obtained from the 2‐mm sieved soils showed that the pressure plate method overestimates θ at low ψ values. The σa(θ) relationship was well described by a simple power expression (R2 > 0·95), in which the power factor, defined as tortuosity, ranged between 1·18 and 3·75. Copyright © 2011 John Wiley & Sons, Ltd.  相似文献   

18.
Tholeiitic basalt glasses from the FAMOUS area of the Mid-Atlantic Ridge are among the most primitive basaltic liquids reported from the ocean basins. One of the more primitive of these[Mg/(Mg+Fe2+) = 0.68;Ni= 232ppm;TiO2 = 0.61] glasses (572-1-1) was selected for an experimental investigation. This study found olivine to be the liquidus phase from 1 atm to 10.5 kbar where it is replaced by clinopyroxene. The sequence of appearance of phases at 1 atm pressure is olivine (1268°C), plagioclase (1235°C) and clinopyroxene (1135°C). The sample is multiply saturated at 10.5 kbar with olivine (Fo88), clinopyroxene (Wo32En60Fs9), and orthopyroxene (Wo5En83Fs12). From the 1-atm data we have measured (FeO/MgO) olivine/(FeO*/MgO) liquid (K′D) for olivine-melt pairs equilibrated at 12 temperatures in the range 1268–1205°C.K′D varies from 0.30 at 1205°C to 0.27 at 1268°C. Analysis of high-pressure olivine melt pairs indicates a systematic increase inK′D with pressure.Evaluation of the 1-atm experiments reveals that fractionation of olivine followed by olivine + plagioclase can generate much of the variation in major element chemistry observed in the FAMOUS basalt glasses. However, it cannot account for the entire spectrum of glass compositions — particularly with respect to TiO2 and Na2O. The variations in these components are such as to require different primary liquids.Comparison of clinopyroxene microphenocrysts/xenocrysts found in oceanic tholeiites with experimental clinopyroxenes reveal that the majority of those in the tholeiites may have crystallized from the magma at pressures greater than ～ 10 kbar and are not accidental xenocrysts. Clinopyroxene fractionation at high pressures may be a viable mechanism for fractionating basaltic magmas.The major and minor element mineral/meltK′d's from our experiments have been used to model the source region residual mineralogy for given percentages of partial melting. These data suggest that ～20% partial melting of a lherzolite source containing 0–10% clinopyroxene can generate the major and minor element concentrations in the parental magmas of the Project FAMOUS basalt glasses.  相似文献   

19.
Discrete Quaternary (<400 ka) tephra fallout layers (mostly <1 cm thick) within the siliceous oozes of the central Mariana Trough at 18°N are characterized by medium-K to high-K subalkalic volcanic glasses (K2O=0.8–3.2 wt.%) with high large-ion lithophile elements (LILE)/high-field-strength elements (HFSE) ratios and Nb depletion (Ba/La35; Ba/Zr3.5; La/Nb4) typical for convergent margin volcanic rocks. Compositional zoning within layers ranges from basaltic to dacitic (SiO2=48–71 wt.%; MgO=0.7–6.5 wt.%); all layers contain basaltic andesites. The tephra layers are interpreted as single explosive eruptive events tapping chemically zoned reservoirs, the sources being the Mariana arc volcanoes (MAV) due to their proximity (100–400 km) and similar element ratios (MAV: Ba/La=36±7; Ba/Zr=3.5±0.9). The glasses investigated, however, contrast with the contemporaneous basaltic to dacitic lavas of the MAV by being more enriched in TiO2 (1.2 wt.%; MAV0.8 wt.%), FeO* (10 wt.%, MAV8–9 wt.%), K2O (1.1 wt.%; MAV0.8 wt.%) and P2O5 (0.4 wt.%; MAV0.2 wt.%). (Semi-)Incompatible trace elements (including Rare Earth Elements (REE)) of the basaltic-andesitic and dacitic glasses match those of the dacitic MAV lavas, which became enriched by fractional crystallization. Moreover, the glasses follow a tholeiitic trend of fractionation in contrast to MAV transitional trends and have a characteristic P2O5 trend that reaches a maximum of 0.6 wt.% P2O5 at 57 wt.% SiO2, whereas MAV lavas increase linearly in P2O5 from 0.1 to 0.3 wt.% with increasing silica. Both explosive and effusive series are interpreted to have evolved in common magma reservoirs by convective fractionation. Similar parental magmas are suggested to have separated into coexisting Si-andesitic to dacitic and basaltic melts by in situ crystallization. The differentiated melt is interstitial in an apatite-saturated crystalline mush of plag+px±ox±ol at the cooler chamber margins in contrast to the less differentiated basaltic to basaltic-andesitic magmas, which are not yet saturated in apatite and occupy the chamber interior. Reinjection of interstitial melt into the chamber interior and mixing with larger melt fractions of the interior liquid (mixing ratios about 1: 8–9) can explain the paradoxical behavior of apatite-controlled P and MREE variation in the basaltic andesite glasses and their MAV dacite-like fractionation patterns. The process may also account for the exclusively tholeiitic trend of fractionation of the glass shard series, but in situ crystallization alone cannot cause their absolute enrichment in (semi-)incompatible elements. The newly mixed melt is suggested to form the basaltic end member of the glass shard series. However, it must have become physically separated from the main MAV magma body (possibly by density-driven convective fractionation) in order to allow for further evolution of the contrasting geochemical paths as well as differentiation.  相似文献   

20.
We present the main seismological results of our study of the Campania-Lucania earthquake of 23 November 1980. A complete set of far field and local data has been analysed. From long-period body waves data we determine the fault plane solution (φ1 = 140°,δ1 = 60°,φ2 = 75°,δ2 = 54°), a depth of 15 km and calculate a seismic moment of 6 × 1025 dyne cm and a source duration of 6 s. From data of a local network deployed immediately after the event we determine aftershock locations: they are aligned in a direction NW-SE that fit extremely well with the focal solution determined above. We can choose as fault plane the plane striking 140° and dipping at 60° and the event is a normal event with a large component of left-lateral strike slip. The source area evaluated from this aftershock distribution 14 km × 40 km is quite suitable for an earthquake of a seismic moment of 6 × 1025 dyne cm.  相似文献   

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