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1.
Photochemistry of Ions at D-region Altitudes of the Ionosphere: A Review   总被引：2，自引：2，他引：0  
The current state of knowledge of the D-region ion photochemistry is reviewed. Equations determining production rates of electrons and positive ions by photoionization of atmospheric neutral species are presented and briefly discussed. Considerable attention is given to the progress in the chemistry of O+(4S), O+(2D), O+(2P), N+, N2 +, O2 +, NO+, N4 +, O4 +, NO+(N2), NO+(CO2), NO+(CO2)2, NO+(H2O) n for n = 1–3, NO+(H2O)(N2), NO+(H2O)2(N2), NO+(H2O)(CO2), NO+(H2O)2(CO2), O2 +(H2O), H3O+(OH), H+(H2O) n for n = 1–8, O?, O2 ?, O3 ?, O4 ?, OH?, CO3 ?, CO4 ?, NO2 ?, NO3 ?, ONOO?, Cl?, Cl?(H2O), Cl?(CO2), HCO3 ?, CO3 ?(H2O), CO3 ?(H2O)2, NO3 ?(H2O), NO3 ?(H2O)2, OH?(H2O), and OH?(H2O)2 ions. The analysis of the D-region rocket ion mass spectrometer measurements shows that, among these ions, O2 +, NO+, NO+(H2O), and H+(H2O) n for n = 1–7 can make the main contribution to the total positive ion number density, and O?, O2 ?, Cl?, OH?(H2O), CO3 ?, HCO3 ?, NO3 ?, ONOO?, CO4 ?, NO3 ?(H2O), NO3 ?(H2O)2, and 35Cl?(CO2) ions can be responsible for the main contribution to the total negative ion number density. Photodetachment of electrons from O?, Cl?, O2 ?, O3 ?, OH?, NO2 ?, and NO3 ?, dissociative electron photodetachment of O4 ? and OH?(H2O), and photodissociation of O3 ?, O4 ?, CO3 ?, CO4 ?, ONOO?, HCO3 ?, CO3 ?(H2O), NO3 ?(H2O), O2 +(H2O), O4 +, N4 +, NO+(H2O), NO+(H2O)2, H+(H2O) n for n = 2–4, NO+(N2), and NO+(CO2) are studied, and the photodetachment and photodissociation rate coefficients are calculated using the current state of knowledge on the cross sections of these processes and fluxes of solar radiation.  相似文献   

2.
The flow of carbon and nitrogen in sediments of the far northern and northern sections of the Great Barrier Reef continental shelf was examined. Most of the organic carbon (81–94%) and total nitrogen (74–92%) depositing to the seabed was mineralized, with burial of carbon (6–19%) and nitrogen (8–20%) being proportionally less on this tropical shelf compared with other non-deltaic shelves. Differences in carbon and nitrogen mineralization among stations related best to water depth and proximity to river basins, with rates of mineralization based on net ∑CO2 production ranging from 17 to 39 ( mean=23) mmol C m−2 d−1. The overall ratio of O2:CO2 flux was 1.3, close to the Redfield ratio, implying that most organic matter mineralized was algal. Sulfate reduction was estimated to account for ≈30% (range: 6–62%), and denitrification for ≈5% (range: 2–13%), of total C mineralization; there was no measurable CH4 production. Discrepancies between ∑CO2 production across the sediment–water interface and sediment incubations suggest that as much as 5 mmol m−2 d−1 (≈25% of ∑CO2 flux) was involved in carbonate mineral formation. Most microbial activity was in the upper 20 cm of sediment. Rates of net NH4+ production ranged from 1.6 to 2.7 mmol N m−2 d−1, with highly variable N2 fixation rates contributing little to total N input. Ammonification and nitrification rates were sufficient to support rapid rates of denitrification (range: 0.1–12.4 mmol N m−2 d−1). On average, nearly 50% of total N input to the shelf sediment was denitrified. The average rates of sedimentation, mineralization, and burial of C and N were greater in the northern section of the shelf than in the far northern section, presumably due to higher rainfall and river discharge, as plankton production was similar between regions. The relative proportion of plankton primary production remineralized at the seafloor was in the range of 30–50% which is at the high end of the range found on other shelves. The highly reactive nature of these sediments is attributed to the deposition of high-quality organic material as well as to the shallowness of the shelf, warm temperatures year-round, and a variety of physical disturbances (cyclones, trawling) fostering physicochemical conditions favorable for maintaining rapid rates of microbial metabolism. The rapid and highly efficient recycling of nutrients on the inner and middle shelf may help to explain why the coral reefs on the outer shelf have remained unscathed from increased sediment delivery since European settlement.  相似文献   

3.
Soils release more carbon, primarily as carbon dioxide (CO2), per annum than current global anthropogenic emissions. Soils emit CO2 through mineralization and decomposition of organic matter and respiration of roots and soil organisms. Given this, the evaluation of the effects of abiotic factors on microbial activity is of major importance when considering the mitigation of greenhouse gases emissions. Previous studies demonstrate that soil CO2 emission is significantly affected by temperature and soil water content. A limited number of studies have illustrated the importance of bulk density and soil surface characteristics as a result of exposure to rain on CO2 emission, however, none examine their relative importance. Therefore, this study investigated the effects of soil compaction and exposure of the soil surface to rainfall and their interaction on CO2 release. We conducted a factorial laboratory experiment with three soil types after sieving (clay, silt and sand soil), three different bulk densities (1·1 g cm–3, 1·3 g cm–3, 1·5 g cm–3) and three different exposures to rainfall (no rain, 30 minutes and 90 minutes of rainfall). The results demonstrated CO2 release varied significantly with bulk density, exposure to rain and time. The relationship between rain exposure and CO2 is positive: CO2 emission was 53% and 42% greater for the 90 minutes and 30 minutes rainfall exposure, respectively, compared to those not exposed to rain. Bulk density exhibited a negative relationship with CO2 emission: soil compacted to a bulk density of 1·1 g cm–3 emitted 32% more CO2 than soil compacted to 1·5 g cm–3. Furthermore we found that the magnitude of CO2 effluxes depended on the interaction of these two abiotic factors. Given these results, understanding the influence of soil compaction and raindrop impact on CO2 emission could lead to modified soil management practices which promote carbon sequestration. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

4.
The influence of atmospheric solar radiation absorption on the photodetachment, dissociative photodetachment, and photodissociation rate coefficients (photodestruction rate coefficients) of O?, Cl?, O2 ?, O3 ?, OH?, NO2 ?, NO3 ?, O4 ?, OH?(H2O), CO3 ?, CO4 ?, ONOO?, HCO3 ?, CO3 ?(H2O), NO3 ?(H2O), O2 +(H2O), O4 +, N4 +, NO+(H2O), NO+(H2O)2, H+(H2O) n for n = 2–4, NO+(N2), and NO+(CO2) at D-region altitudes of the ionosphere is studied. A numerical one-dimensional time-dependent neutral atmospheric composition model has been developed to estimate this influence. The model simulations are carried out for the geomagnetically quiet time period of 15 October 1998 at moderate solar activity over the Boulder ozonesonde. If the solar zenith angle is not more than 90° then the strongest influence of atmospheric solar radiation absorption on photodestruction of ions is found for photodissociation of CO4 ? ions when CO3 ? ions are formed. It follows from the calculations that decreases in the photodestruction rate coefficients of ions under consideration caused by this influence are less than 2 % at 70 km altitude and above this altitude if the solar zenith angle does not exceed 90°.  相似文献   

5.
Abstract

The deposition of chemical elements in a catchment occurs through three different processes: wet, dry and cloud deposition. Total deposition cannot be inferred from measurements made with open-field raingauges, and still constitutes a challenge to scientific method. The chemical composition of samples from an open-field raingauge (bulk precipitation) was analysed over a period of several years in a small Mediterranean catchment in the Maures Massif, France. The input of chloride measured in this way was two times lower than the output, despite the fact that this element is reputed to be conservative, which means input and output should roughly balance. This implies that input has previously been underestimated. Analysis of the bulk precipitation data was carried out taking into account both the history of rain events and of sampling. This study allowed the relative parts of the different deposition processes to be quantified. Dry deposition can provide from 20% to more than 80% of the anthropogenic and terrigenic elements (Ca2+, Mg2+, K+, NO3 ?, SO4 2-, SiO2) to the rain samples. The occult deposition of marine elements on the catchment area (50% of total deposition) was found to be mostly due to cloud deposition during wet periods.  相似文献   

6.
为揭示太湖流域降雨和湖水酸根阴离子长期变化特征及环境意义,通过历史数据收集和采样分析,对太湖流域降雨和湖水中的SO42-、NO3-变化特征和来源进行了研究.结果表明：自1990s以来太湖流域降雨中SO42-呈显著下降趋势,年平均下降率为0.28 mg/（L·a）;NO3-浓度却呈显著上升趋势,年平均增长率为0.05 mg/（L·a）,降雨中氮污染呈现加重的趋势.与之相反,湖水中SO42-呈显著上升趋势,年平均增长率为1.24 mg/（L·a）;NO3-浓度却呈显著下降趋势,年平均下降率为0.02 mg/（L·a）.30年以来,太湖水体SO42-/NO3-比值不断升高,远高于降水SO42-/NO3-比值.研究认为：流域SO2排放引起的酸沉降是湖水SO42-浓度增长的最重要原因,但氮氧化物排放并未引起湖水NO3-浓度升高,说明太湖流域对大气沉降的氮氧化物有滞留作用,而太湖水体是流域大气沉降硫酸盐的重要汇.综合治理太湖流域酸性物质排放对防止太湖水体酸化和治理富营养化都具有重要意义.  相似文献   

7.
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   

8.
Dew samples were collected between October 2007 and February 2008 from a suburban site in Agra. pH, conductivity, major inorganic ions (F?, Cl?, NO 3 ? , SO 4 2? , Na+, K+, Ca2+, Mg2+, and NH 4 + ), and some trace metals (Cr, Sn, Zn, Pb, Cd, Ni, Mn, Fe, Si, Al, V, and Cu) were determined to study the chemistry of dew water. The mean pH was 7.3, and the samples exhibited high ionic concentrations. Dew chemistry suggested both natural and anthropogenic influences, with acidity being neutralized by atmospheric ammonia and soil constituents. Ion deposition flux varied from 0.25 to 3.0?neq?m?2?s?1, with maximum values for Ca2+ followed by NH 4 + , Mg2+, SO 4 2? , Cl?, NO 3 ? , Na+, K+, and F?. Concentrations of trace metals varied from 0.13 to 48?μg?l?1 with maximum concentrations of Si and minimum concentration of Cd. Correlation analysis suggested their contributions from both crustal and anthropogenic sources.  相似文献   

9.
Noncondensible gases from hot springs, fumaroles, and deep wells within the Valles caldera geothermal system (210–300°C) consist of roughly 98.5 mol% CO2, 0.5 mol% H2S, and 1 mol% other components. 3He/4He ratios indicate a deep magmatic source (R/Ra up to 6) whereas δ13C–CO2 values (−3 to −5‰) do not discriminate between a mantle/magmatic source and a source from subjacent, hydrothermally altered Paleozoic carbonate rocks. Regional gases from sites within a 50-km radius beyond Valles caldera are relatively enriched in CO2 and He, but depleted in H2S compared to Valles gases. Regional gases have R/Ra values ≤1.2 due to more interaction with the crust and/or less contribution from the mantle. Carbon sources for regional CO2 are varied. During 1982–1998, repeat analyses of gases from intracaldera sites at Sulphur Springs showed relatively constant CH4, H2, and H2S contents. The only exception was gas from Footbath Spring (1987–1993), which experienced increases in these three components during drilling and testing of scientific wells VC-2a and VC-2b. Present-day Valles gases contain substantially less N2 than fluid inclusion gases trapped in deep, early-stage, post-caldera vein minerals. This suggests that the long-lived Valles hydrothermal system (ca. 1 Myr) has depleted subsurface Paleozoic sedimentary rocks of nitrogen. When compared with gases from many other geothermal systems, Valles caldera gases are relatively enriched in He but depleted in CH4, N2 and Ar. In this respect, Valles gases resemble end-member hydrothermal and magmatic gases discharged at hot spots (Galapagos, Kilauea, and Yellowstone).  相似文献   

10.
Diffuse CO<Subscript>2</Subscript> degassing at Vesuvio,Italy   总被引：1，自引：0，他引：1  
At Vesuvio, a significant fraction of the rising hydrothermal–volcanic fluids is subjected to a condensation and separation process producing a CO2–rich gas phase, mainly expulsed through soil diffuse degassing from well defined areas called diffuse degassing structures (DDS), and a liquid phase that flows towards the outer part of the volcanic cone. A large amount of thermal energy is associated with the steam condensation process and subsequent cooling of the liquid phase. The total amount of volcanic–hydrothermal CO2 discharged through diffuse degassing has been computed through a sequential Gaussian simulation (sGs) approach based on several hundred accumulation chamber measurements and, at the time of the survey, amounted to 151 t d–1. The steam associated with the CO2 output, computed assuming that the original H2O/CO2 ratio of hydrothermal fluids is preserved in fumarolic effluents, is 553 t d–1, and the energy produced by the steam condensation and cooling of the liquid phase is 1.47×1012 J d–1 (17 MW). The location of the CO2 and temperature anomalies show that most of the gas is discharged from the inner part of the crater and suggests that crater morphology and local stratigraphy exert strong control on CO2 degassing and subsurface steam condensation. The amounts of gas and energy released by Vesuvio are comparable to those released by other volcanic degassing areas of the world and their estimates, through periodic surveys of soil CO2 flux, can constitute a useful tool to monitor volcanic activity.Editorial responsibility: H. Shinohara  相似文献   

11.
Ni-rich spinels have been found throughhout the world at the Cretaceous-Tertiary boundary. These minerals have no counterparts in terrestrial rocks but have been observed in meteoroid ablation material and impact debris, suggesting that the Cretaceous-Tertiary boundary spinels result from an extraterrestrial event. Their stratigraphic distribution, which has been observed at the Cretaceous-Tertiary boundary sites of El Kef (Tunisia), Caravaca (Spain) and Hole 761C (ODP Leg 122, Indian Ocean), are markedly different from site to site and are all much less extended than the Ir anomalies. Regional differences in Ni-rich spinel distibution are entirely explained by a brief event recorded under different bioturbation conditions. The wider stratigraphic dispersion of Ir is attributed to postdepositional chemical processes. At El Kef, the site which appears to be the least affected by bioturbation and which has the highest sedimentation rate, the 1–2 mm thick Ni-rich spinel spike indicates that the deposition time did not exceed an upper limit of 100 years. This upper limit is consistent only with the collision of an asteroid or a comet at the close of the Cretaceous.  相似文献   

12.
Ion composition measurements on board the ACTIVE satellite during the recovery phase of a strong geomagnetic storm of 10–12 April 1990 revealed extremely high concentrations (up to 103 cm−3) of the NO+, O+2, N+2 molecular ions in the topside F2-region of the European high-latitude zone. Concentrations of O+, N+, He+, H+ light ions were slightly decreased relative to prestorm quite conditions. Theoretical calculations were used to analyze the observed variations in ion concentration. Increased neutral temperature and [O2], [N2] are shown to be the main reasons for the observed ion concentration variations.  相似文献   

13.
The Yangyi geothermal field, located 72 km northwest to Lhasa City, capital of Tibet, has a high reservoir temperature up to at least 207.2 °C. The geothermal waters from both geothermal wells and hot springs belong to the HCO3 (+CO3)–Na type. Factor analysis of all the chemical constituents shows that they can be divided into two factors: F1 factor receives the contributions of SO42−, Cl−, SiO2, As, B, Na+, K+, and Li+; whereas F2 factor is explained by HCO3−, F−, CO32−, Ca2+, and Sr2+. The F1 factor can be regarded as an indicator of the reservoir temperature distribution at Yangyi, but its variable correlation with the results of different geothermometers (Na–K, quartz and K–Mg) does not allow one to draw further inferences. Different from F1, the F2 factor is an indicator of a group of hydrogeochemical processes resulting from the CO2 pressure decrease in geothermal water during its ascent from the deep underground, including transformation of HCO3− to CO32−, precipitation of Ca2+ and Sr2+, and release of F− from some fluoride-bearing minerals of reservoir rocks. The plot of enthalpy vs. chloride, prepared on the basis of Na–K equilibrium temperatures, suggests that a parent geothermal liquid (PGL) with Cl− concentration of 185 mg/L (that of sample YYT-8) and enthalpy of 1020 J/g (corresponding to a temperature of 236–237 °C, i.e., somewhat higher than that of sample YYT-6) is present in the geothermal reservoir of the Yangyi area, below both the Qialagai valley and the Bujiemu valley, although the samples less affected by mixing and cooling (YYT-6 and YYT-7) come from the second site. The discharge of geothermal waters with high contents of toxic elements such as B, As and F into the Luolang River, the only drinking water source for local residents, has caused slight pollution of the river water. Great care should therefore be taken in the geothermal water resource management at Yangyi.  相似文献   

14.
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   

15.
Ambient concentrations of sulfur dioxide (SO2), nitrogen dioxide (NO2), and ozone (O3) were measured at 51 sampling points by passive sampling technique in Kocaeli, an important industrial city in Turkey. Samples were analyzed by UV‐spectrophotometry for NO2 and O3 and by ion chromatography for SO2, respectively. Concentrations of SO2, NO2, and O3 were determined to investigate their spatial distribution and source characterization. The sampling campaigns revealed an average concentration of 8 µg/m3 (max. 82 µg/m3) for SO2, and 14 µg/m3 (max. 40 µg/m3) for NO2, in summer; while average winter concentrations were 25 µg/m3 (max. 61 µg/m3) for SO2, and 50 µg/m3 (max. 100 µg/m3) for NO2. The maximum ozone concentrations were determined to be 86 µg/m3 in summer and 61 µg/m3 in winter downwind of the source areas of the precursor pollutant emissions. The results showed that NO2 and SO2 concentrations in industrial and urban areas were two to four times higher compared with rural areas in the summer and winter. In the light of the information obtained from the spatial interpolation of the pollutant concentrations, a selection of appropriate locations for continuous monitoring was suggested according to the European Community (EU) directives.  相似文献   

16.
18O/16O data from the 200-m-thick, 0.76 Ma Bishop Tuff outflow sheet provide evidence for a vigorous, short-lived (≈10 years), high-temperature, fumarolic meteoric–hydrothermal event. This is proved by: (1) the juxtaposition in the upper, partially welded Bishop Tuff of low-18O groundmass/glass (δ18O=−5 to +3) with coexisting quartz and feldspar phenocrysts having magmatic δ18O values (+8.7±0.3; +7.5±0.3); and (2) the fact that these kinds of 18O/16O signatures correlate very well with morphological features and mapped zones of fumarolic activity. Profiles of δ18O with depth in the Bishop Tuff within the fumarole area define a 40- to 50-m-thick, low-18O, stratigraphic zone that is sandwiched between the essentially unwelded near-surface portion of the tuff and an underlying, densely welded black tuff that displays magmatic 18O/16O values. Shallow-dipping columnar joints and other fumarolic features (i.e., subhorizontal tubular conduits and steep fissures) correlate very well with these pervasively devitrified, low-18O zones. The base of the low-18O zone is extremely sharp (3‰ per meter) and is located directly above the transition from partially welded tuff to densely welded black tuff. The observed average whole-rock 18O-depletions within this low-18O zone are about 6–7‰, requiring meteoric water/rock ratios in excess of 0.24 in mass units. Rainfall on the surface of the tuff would not have been high enough to supply this much H2O in the short lifetime of fumarolic activity, suggesting that some recharge must have been from groundwater flow through the upper part of the tuff, above the sloping (1°–5°) top of the impermeable lower zone. This is compatible with the observation that the fumarolic areas roughly correlate with the preeruptive regional drainage pattern. Some of this recharge may in part have been from the lake that filled Long Valley caldera, which was dammed by the Bishop Tuff up to the level of this boundary between the partially and densely welded zones (≈7000 ft, the elevation of the highest Long Valley Lake shorelines). Gazis et al. had previously shown that the 2.8-Ma intracaldera Chegem Tuff from the Caucasus Mountains exhibits exactly the same kind of 18O-signature that we have correlated with fossil fumaroles in the Bishop Tuff outflow sheet. Although not recognized as such by McConnell et al.; 18O/16O data from drill-hole samples from the intracaldera Bishop Tuff in Long Valley also display this characteristic 18O signature (i.e., analogous δ18O-depth profiles, as well as low-18O groundmass coexisting with high-18O feldspar phenocrysts). This fumarolic 18O/16O signature is observed to much greater depths (≈650–750 m) in the intracaldera tuffs (≈1500 m thick) than it is in the ≈200-m-thick Bishop Tuff outflow sheet (≈80 m depth).  相似文献   

17.
Although riparian zones are well known to reduce nitrogen (N) and phosphorus (P) runoff to streams, they also have the potential to affect greenhouse gas (CO2, N2O, and CH4) fluxes to the atmosphere. Following large storms, soil biogeochemical conditions often become more reduced, especially in oxbow depressions and side channels, which can lead to hot moments of greenhouse gas production. Here, we investigate the impact of the remnants of Hurricane Irene and Tropical Storm Lee on riparian zone hydrology (water table: WT), and biogeochemistry (oxidation‐reduction potential [ORP], dissolved oxygen [DO], NO3?, PO43?, CO2, N2O, CH4). Results indicate that large storms have the potential to reset WT levels for weeks to months. Overbank flooding at our site following Irene and Lee led to the infiltration of well‐oxygenated water at depth (higher DO and ORP) while promoting the development of anoxic conditions within soil aggregates near the soil surface (increased N2O and CH4 fluxes). A short‐term increase in CO2 emission was observed following Irene at our site where aerobic respiration was water‐limited. Over a 2‐year period, an oxbow depression exhibited higher WT, higher N2O and CH4 fluxes (hot moment), higher CO2 fluxes (seasonal), and lower NO3? concentrations (seasonal) than the rest of the riparian zone. However, neither Irene, nor Lee, nor the oxbow depression significantly impacted PO43?. Dissolved organic carbon, ORP, and DO data illustrate the time‐lag (>20 years) between the creation of an oxbow depression and the development of reducing conditions despite clear differences in riparian zone and oxbow WT dynamics.  相似文献   

18.
Several kinds of geochemical anomaly before strong earthquakes have been observed in China since 1966. They include changes in groundwater radon levels, ion content of water (Ca+2, Mg+2, Cl–, SO 4 –2 , F–), dissolved gases (H2, CO2), and gases escaping from the aeration zone through abandoned dry wells (Ar, N2, CO2). The radon anomalies may be grouped as long-term and short-term anomalies. Most of the geochemical anomalies observed are characterized by a pattern of increase. The largest amplitude recorded was 37 times the base level. Preliminary study indicates that the types of seismogeochemical anomaly observed prior to strong earthquakes depend on tectonic, geologic, lithologic, and hydrogeological conditions at the monitoring station. Results obtained from modelling experiments on the mechanisms of some anomalies are given.  相似文献   

19.
Three techniques for obtaining soil water solutions (gravitational and matrical waters extracted using both in situ tension lysimeters and in vitro pressure chambers) and their later chemical analysis were performed in order to know the evolution of the soil‐solution composition when water moves down through the soil, from the Ah soil horizon to the BwC‐ or C‐horizons of forest soils located in western Spain. Additionally, ion concentrations and water volumes of input waters to soil (canopy washout) and exported waters (drainage solutions from C‐horizons) were determined to establish the net balance of solutes in order to determine the rates of leaching or retention of ions. A generalized process of sorption or retention of most components (even Cl?) was observed, from the soil surface to the C‐horizon, in both gravitational and matrical waters, with H4SiO4, Mn2+, Na+, and SO42? being the net exported components from the soil through the groundwater. These results enhance the role of the recycling effect in these forest soils. The net percentages of elements retained in these forest soils, considering the inputs and the outputs balance, were 68% K+, 85% Ca2+, 58% Mg2+, 7% Al3+, 5% Fe3+, 34% Zn2+, 57% Cl?, and 20% NO3?, and about 75% of dissolved organic carbon was mineralized. Copyright © 2007 John Wiley & Sons, Ltd.  相似文献   

20.
This study uses stable isotopes and major ions to examine the seasonal evolution of penitentes on the surface of Tapado Glacier, in the Norte Chico region of the Chilean Andes. A snow pit was sampled in November 2011, and penitentes were sampled during the summer (December 2011 and January 2012). The major ion load of the winter snowpack is dominated by Ca2+ (60%), SO42? (16%) and NO3? (13%), and there is little influence from marine air masses at the site, with most SO42?, Mg2+, Ca2+ and Na+, derived from non‐sea salt sources. During the early ablation season we observe increases in stable isotope ratios and major ion concentrations (particularly lithic ions Na+, Mg2+ and Ca2+) in the upper reaches of penitentes, which is attributed to sublimation and the aeolian deposition of dust particles. In the late‐summer, melt replaces sublimation as the dominant ablation process and results in smoothing of the stable isotope profile and the elution of major ions within the penitente snow and ice matrix. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

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