On the Kuril Islands there are 85 volcanoes, 39 of which are active. Hot springs and mud pots are wide spread in this area and have significant inputs on the chemical composition of the surrounding surface waters and environment. We present results of trace elements as well as data on H, O, S, and He isotope ratios for hydrothermal systems of the Mendeleev Volcano (Kunashir Island) and surrounding surface waters. Water and gas samples were taken from springs and holes as well as creeks and the Lesnaya River. Among the thermal water types, three main groups can be distinguished. The first group includes the waters, in which SO4^- ion predominant. The water temperature on the surface reaches 97℃, and TDS varies from a few g/L to 7 g/L. These waters are acid to superacid with pH values ranging 0.6 to 2.3. The second group is sodium-chloride waters. A maximum TDS is 14.2 g/L. The waters are neutral or alkaline; pH varies from 6.9 to 8.2. The third group is the sodium-chloride-sulfate-bicarbonate water. The Stolbovskie springs, located in the periphery of the Mendeleev Volcano are representative of this type. The pH of these waters is close to neutral. TDS is 1.9 g/L. They are rather the derivatives of sodium-chloride waters arisen from dilution of them by subsurface waters. The Kuslyi Creek and Lesnaya River are located near the Mendeleev Volcano. The most acid springs discharge into the Kislyi Creek as a result pH of this creek being 2.5, and contents of most elements rather high. For example, the contents of dissolved solids of Si, Fe, Al, Mn, Zn, in waters of the Kislaya Creek are 22.1, 8.1, 6.2, 1.29, and 0.28 mg/L, and correspondently. The water of the Lesnaya River, (Before the Kislyi Creek, pH is about 8 with TDS 102 mg/L, but after the Kuslyi Creek, pH decreases and the concentrations of chemical elements increase. Debit of the Kislayi Creek in summer season is about 370 L/sec. It means that every day only this small creek inputs in the Lesnay River about 706 kg of Si; 相似文献
Photodegradation of chrysene, benzo (a) pyrene and benzo (g, h, i) perylene in natural water of the Yellow River was studied using simulation sunlight. The effects of particulates on the photodegradation were explored. Several results arose from this study. (1) The photodegradation of PAHs can be fitted with first-order kinetics when no particulate exists in water system, and the first-order constant increases with decreasing of initial concentration of PAHs. The photodegradation rates of the three PAHs are related to their molecule absorption spectrum. (2) The existence of loess exerts two kinds of effects on the photodegradation of PAHs, including the inner filter effects and the photosensitizing effects of humic substance in loess. These two contrary effects lead to the difference of net effects among different contents of loess. When the loess contents are 0.1 and 5.0 g/L, the existence of loess stimulates the photodegradation of chrysene, benzo (a) pyrene. When the loess content is 5.0 g/L, the existence of loess stimulates the photodegradation of benzo (g, h, i) perylene. In addition, the photodegradation of PAHs can be fitted with the second-order kinetics when there is loess in the water system. (3) The soluble humic substances in loess can accelerate the photodegradation of PAHs while the in soluble part cannot. (4) Since the soluble humic substances in the suspended solids of the river have been dissolved in water, 相似文献
Crystallization under confinement conditions is a very important process in geochemistry and geophysics. Computer simulations of fluids in nanometer scale pore spaces can provide a unique microscopic insight into the structure, dynamics and forces arising from the crystallization process. We discuss in this paper molecular dynamics computer simulations of crystallization in pores of nanometer dimensions. The crystallization pressure due to the freezing of a model of Argon in a nanopore is computed using molecular dynamics simulations. We also investigate the influence of pore geometry in determining the dynamics of confined fluids, as well as mass separation in binary mixtures. It turns out that the pore geometry reveals itself as an important variable, leading to 1) new mechanisms for fast diffusion in confined spaces, and 2) accumulation of solute in specific regions inside the pore. 相似文献
A geoelectrical monitoring activity has been carried out to improve the geological and hydrogeological knowledge about the Varco d'Izzo landslide (Potenza, Basilicata, Southern Apennine, Italy), an active rotational–translational slide evolved in earth-flow. In this work we have focused on the Self-Potential (SP) method by applying three different SP measuring techniques and combining modern technologies for data acquisition and new methods for tomographic inversion. A SP map and three static SP tomographies have been carried out to better analyse the groundwater circulation system and to better reconstruct the geometry of the landslide body. In the accumulation zone, which is the area more exposed to the geomorphological activity, a new SP measuring strategy has been applied. This strategy, based on time-continuous 2D SP tomographies, helps identify water flow changes in subsurface by studying the time series of SP tomographic images. The analysis of time-dependent changes of water infiltration in near surface is the key to better understand the hydrogeological processes underlying the ground instability phenomena. The time-lapse analysis of tomographic images has allowed us not only to investigate the correlation between the temporal changes of SP signals and rainfall events, but also to quantify the range of these changes. The modification of the distribution of the SP source accumulation zones is associated with the dynamics of the groundwater flows. These preliminary results allow us to consider the SP tomographic method as a tool for geophysical monitoring of landslide areas and encourage to develop new measuring systems for near-real time applications. 相似文献
Geochemical analyses and geobarometric determinations have been combined to create a depth vs. radiogenic heat production database for the Sierra Nevada batholith, California. This database shows that mean heat production values first increase, then decrease, with increasing depth. Heat production is 2 μW/m3 within the 3-km-thick volcanic pile at the top of the batholith, below which it increases to an average value of 3.5 μW/m3 at 5.5 km depth, then decreases to 0.5–1 μW/m3 at 15 km depth and remains at these values through the entire crust below 15 km. Below the crust, from depths of 40–125 km, the batholith's root and mantle wedge that coevolved beneath the batholith appears to have an average radiogenic heat production rate of 0.14 μW/m3. This is higher than the rates from most published xenolith studies, but reasonable given the presence of crustal components in the arc root assemblages. The pattern of radiogenic heat production interpreted from the depth vs. heat production database is not consistent with the downward-decreasing exponential distribution predicted from modeling of surface heat flow data. The interpreted distribution predicts a reasonable range of geothermal gradients and shows that essentially all of the present day surface heat flow from the Sierra Nevada could be generated within the 35 km thick crust. This requires a very low heat flux from the mantle, which is consistent with a model of cessation of Sierran magmatism during Laramide flat-slab subduction, followed by conductive cooling of the upper mantle for 70 m.y. The heat production variation with depth is principally due to large variations in uranium and thorium concentration; potassium is less variable in concentration within the Sierran crust, and produces relatively little of the heat in high heat production rocks. Because silica content is relatively constant through the upper 30 km of the Sierran batholith, while U, Th, and K concentrations are highly variable, radiogenic heat production does not vary directly with silica content. 相似文献
The paragenesis of monazite in metapelitic rocks from the contact aureole of the Harney Peak Granite, Black Hills, South Dakota, was investigated using zoning patterns of monazite and garnet, electron microprobe dating of monazite, bulk-rock compositions, and major phase mineral equilibria. The area is characterized by low-pressure and high-temperature metamorphism with metamorphic zones ranging from garnet to sillimanite zones. Garnet porphyroblasts containing euhedral Y annuli are observed from the garnet to sillimanite zones. Although major phase mineral equilibria predict resorption of garnet at the staurolite isograd and regrowth at the andalusite isograd, textural and mass balance analyses suggest that the formation of the Y annuli is not related to the resorption-and-regrowth of garnet having formed instead during garnet growth in the garnet zone. Monazite grains in Black Hills pelites were divided into two generations on the basis of zoning patterns of Y and U: monazite 1 with low-Y and -U and monazite 2 with high-Y and -U. Monazite 1 occurs in the garnet zone and persists into the sillimanite zone as cores shielded by monazite 2 which starts to form in the andalusite zone. Pelites containing garnet porphyroblasts with Y annuli and monazite 1 with patchy Th zoning are more calcic than those with garnet with no Y annuli and monazite with concentric Th zoning. Monazite 1 is attributed to breakdown of allanite in the garnet zone, additionally giving rise to the Y annuli observed in garnet. Monazite 2 grows in the andalusite zone, probably at the expense of garnet and monazite 1 in the andalusite and sillimanite zones. The ages of the two different generations of monazite are within the precision of chemical dating of electron microprobe. The electron microprobe ages of all monazites from the Black Hills show a single ca. 1713 Ma population, close to the intrusion age of the Harney Peak Granite (1715 Ma). This study demonstrates that Y zoning in garnet and monazite are critical to the interpretation of monazite petrogenesis and therefore monazite ages. 相似文献
Ultrahigh-pressure (UHP) metamorphic terranes reflect subduction of continental crust to depths of 90–140 km in Phanerozoic contractional orogens. Rocks are intensely overprinted by lower pressure mineral assemblages; traces of relict UHP phases are preserved only under kinetically inhibiting circumstances. Most UHP complexes present in the upper crust are thin, imbricate sheets consisting chiefly of felsic units ± serpentinites; dense mafic and peridotitic rocks make up less than 10% of each exhumed subduction complex. Roundtrip prograde–retrograde P–T paths are completed in 10–20 Myr, and rates of ascent to mid-crustal levels approximate descent velocities. Late-stage domical uplifts typify many UHP complexes.
Sialic crust may be deeply subducted, reflecting profound underflow of an oceanic plate prior to collisional suturing. Exhumation involves decompression through the P–T stability fields of lower pressure metamorphic facies. Scattered UHP relics are retained in strong, refractory, watertight host minerals (e.g., zircon, pyroxene, garnet) typified by low rates of intracrystalline diffusion. Isolation of such inclusions from the recrystallizing rock matrix impedes back reaction. Thin-aspect ratio, ductile-deformed nappes are formed in the subduction zone; heat is conducted away from UHP complexes as they rise along the subduction channel. The low aggregate density of continental crust is much less than that of the mantle it displaces during underflow; its rapid ascent to mid-crustal levels is driven by buoyancy. Return to shallow levels does not require removal of the overlying mantle wedge. Late-stage underplating, structural contraction, tectonic aneurysms and/or plate shallowing convey mid-crustal UHP décollements surfaceward in domical uplifts where they are exposed by erosion. Unless these situations are mutually satisfied, UHP complexes are completely transformed to low-pressure assemblages, obliterating all evidence of profound subduction. 相似文献