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1.
Stemflow of beech (Fagus sylvatica L.) represents a significant input of water and elements to the soil and might influence the spatial patterns and the rate of seepage fluxes at the stand scale. We investigated the soil solution chemistry at different depths and distances from the stem and the element fluxes with stemflow, throughfall and seepage in proximal and distal stem areas of a 130‐year‐old beech/oak forest in Steigerwald (northern Bavaria, Germany). The proximal stem area (in total 286 m2 ha−1) was defined as a 1 m2, 60 cm deep cylinder around the beech stem. Seepage fluxes were calculated by a soil hydrological model for 1996 using measured soil matrix potentials and tree xylem flow data for calibration. Stemflow represented 6·6% of the annual soil water input. With the exception of H+ fluxes, less than 10% of the total element fluxes with throughfall and stemflow reached the soil via stemflow. The volume‐weighted concentrations of H+, K+ and SO42− in stemflow were higher than those in throughfall, while other elements had similar concentrations. Soil solution K+ concentrations decreased with stem distance, but the Na+, Mg2+, Cl− and SO42− concentrations increased. Gradients for other elements were not statistically significant. Stemflow had a strong influence on the spatial patterns of element fluxes with seepage. The water fluxes through the soil of the proximal stem areas at a depth of 60 cm contributed 13·5% to the total seepage at the stand scale. Proximal to the stems about 20% of total seepage for K+, Mn2+, Aln+, dissolved organic N and dissolved organic C were concentrated, but only 8–10% for Na+, Mg2+ and Ca2+. The loss of acid‐neutralizing capacity calculated from the flux balance was about four times higher proximal to the stems compared with distal areas, indicating high rates of soil acidification proximal to the stems. Our results confirm the concept of a microsite around beech stems, characterized by high element and water fluxes in comparison with distal stem areas. Calculations of seepage fluxes and element budgets in beech stands have to consider the spatial heterogeneity of fluxes induced by stemflow. Copyright © 2000 John Wiley & Sons, Ltd. 相似文献
2.
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
3.
Water and nutrient fluxes were studied during a 12-month period in an alerce (Fitzroya cupressoides) forest, located in a remote site at the Cordillera de la Costa (40°05′S) in southern Chile. Measurements of precipitation, throughfall, stemflow, effective precipitation, soil infiltration and stream flow were carried out in an experimental, small watershed. Simultaneously, monthly water samples were collected to determine the concentrations and transport of organic-N, NO3-N, total-P, K+, Ca2+, Na+ and Mg2+ in all levels of forest. Concentration of organic-N, NO3-N, total-P and K+ showed a clear pattern of enrichment in the throughfall, stemflow, effective precipitation and soil infiltration. For Ca2+ and Mg2+, enrichment was observed in the effective precipitation, soil infiltration and stream flow. Annual transport of K+, Na+, Ca2+ and Mg2+ showed that the amounts exported from the forest via stream flow (K+=0·95, Na+=32·44, Ca2+=8·76 and Mg2+=7·16 kg ha−1 yr−1) are less than the inputs via precipitation (K+=6·39, Na+=40·99, Ca2+=15·13 and Mg2+=7·61 kg ha−1 yr−1). The amounts of organic-N and NO3-N exported via stream flow (organic-N=1·04 and No3-N=3·06 kg ha−1 yr−1) were relatively small; however, they represented greater amounts than the inputs via precipitation (organic-N=0·74 and NO3-N=0·97 kg ha−1 yr−1), because of the great contribution of this element in the superficial soil horizon, where the processes of decomposition of organic material, mineralization and immobilization of the nutrients occurs. © 1998 John Wiley & Sons, Ltd. 相似文献
4.
A. V. Pavlov 《Surveys in Geophysics》2012,33(5):1133-1172
The current state of knowledge of E- and F-region ion chemistry is reviewed. Considerable attention is given to the progress in the chemistry of unexcited N2 +, O2 +, NO+, O+(4S), N+, H+, He+, Fe+, Mg+, Na+, Ca+, and K+ ions and electronically excited O+(2D), O+(2P), O+(4P), and $ {\text{O}}^{ + } (^{2} {\text{P}}^{*} ) $ ions. Achievements in our understanding of the role of vibrationally excited N2 +, O2 +, and NO+ ions in the ionosphere are discussed. 相似文献
5.
Salinity in Soils and Tsunami Deposits in Areas Affected by the 2010 Chile and 2011 Japan Tsunamis 总被引：1，自引：0，他引：1
Takumi Yoshii Masahiro Imamura Masafumi Matsuyama Syunichi Koshimura Masashi Matsuoka Erick Mas Cesar Jimenez 《Pure and Applied Geophysics》2013,170(6-8):1047-1066
The accumulation of data sets of past tsunamis is the most basic but reliable way to prepare for future tsunamis because the frequency of tsunami occurrence and their magnitude can be estimated by historical records of tsunamis. Investigation of tsunami deposits preserved in geological layers is an effective measure to understand ancient tsunamis that occurred before historical records began. However, the areas containing tsunami deposits can be narrower than the area of tsunami inundation, thus resulting in underestimation of the magnitude of past tsunamis. A field survey was conducted after the 2010 Chile tsunami and 2011 Japan tsunami to investigate the chemical properties of the tsunami-inundated soil to examine the applicability of tsunami inundation surveys considering water-soluble salts in soil. The soil and tsunami deposits collected in the tsunami-inundated areas are rich in water-soluble ions (Na+, Mg2+, Cl?, Br? and SO 4 2? ) compared with the samples collected in the non-inundated areas. The analytical result that the ratios of Na+, Mg2+, Br? and SO 4 2? to Cl? are nearly the same in the tsunami deposits and in the tsunami-inundated soil suggests that the deposition of these ions resulting from the tsunami inundation does not depend on whether or not tsunami deposits exist. Discriminant analysis of the tsunami-inundated areas using the ion contents shows the high applicability of these ions to the detection of tsunami inundation during periods when the amount of rainfall is limited. To examine the applicability of this method to palaeotsunamis, the continuous monitoring of water-soluble ions in tsunami-inundated soil is needed as a future study. 相似文献
6.
This study examined the stream chemistry changes in Staunton River (a second‐order headwater stream with an average annual discharge 704 m3 ha?1 yr?1, Shenandoah National Park, Virginia) resulting from a catastrophic flood in June 1995. This flood, which followed after 800 mm of rain in a 4‐day period, caused large‐scale debris flows and complete scouring of riparian soils down to bedrock in the lower 2 km of the stream, and has been estimated to be a 1000‐year flood. The flood affected stream chemistry on both short‐ and long‐term time scales. The primary short‐term response was elevations in stream concentration of Ca2+, Mg2+, and K+ by 59%, 87%, and 49%, respectively, for 6 months immediately following the flood. The long‐term impact of decreased concentration of all base cations and SiO2 during summer months (8% average) lasted about 2 years. At the episodic time scale, Ca2+, Mg2+, and K+ flushed from soil sources during pre‐flood storms while Na+ and SiO2 diluted; these trends generally reversed during post‐flood storms for 2 years. Short‐term effects are attributed to the leaching of unconsolidated soil and upturned organic matter that clogged the streambed after the flood. The long‐term and superimposed episodic impacts may have resulted from the loss of riparian soils and vegetation in the flood. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
7.
A. V. Pavlov 《Surveys in Geophysics》2014,35(2):259-334
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
8.
Anita Lakhani Ravindra Singh Parmar Satya Prakash 《Pure and Applied Geophysics》2012,169(5-6):859-871
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.
A. V. Pavlov 《Surveys in Geophysics》2016,37(4):811-844
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
10.
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
11.
Thermokarst lakes play a key role in the hydrological and biogeochemical cycles of permafrost regions. Current knowledge regarding the changes caused by permafrost degradation to the hydrochemistry of lakes in the Qinghai-Tibet Plateau (QTP) is limited. To address this gap, a systematic investigation of thermokarst lake water, suprapermafrost water, ground ice, and precipitation was conducted in the hinterland of the QTP. The thermokarst lake water in the QTP was identified to be of the Na-HCO3-Cl type. The mean concentrations of HCO3− and Na+ were 281.8 mg L−1 (146.0–546.2 mg L−1) and 73.3 mg L−1 (9.2–345.8 mg L−1), respectively. The concentrations of Li+, NH4+, K+, F−, NO2−, and NO3− were relatively low. Freeze-out fractionation concentrated the dissolved solids within the lake water during winter, which was deeply deepened on lake depth and lake ice thickness. Owing to solute enrichment, the ground ice was characterized by high salinity. Conversely, repeated replenishment via precipitation led to lower solute concentrations in the ground ice near the permafrost table compared to that within the permafrost. Although lower solute concentration existed in precipitation, the soil leaching and saline ground ice melting processes enhanced the solute load in suprapermafrost water, which is considered an important water and solute resource in thermokarst lakes. The influencing mechanism of permafrost degradation on thermokarst lake hydrochemistry is presumably linked to: (1) the liberation of soluble materials sequestered in ground ice; (2) the increase of solutes in suprapermafrost water and soil pore water; and (3) the changes in lake morphometry. These results have major implications on the understanding of the effects of ground ice melting on ecosystem functions, biogeochemical processes, and energy balance in a rapidly changing climate. 相似文献
12.
Groundwater salinization has become a crucial environmental problem worldwide and is considered the most widespread form of groundwater contamination in the coastal zone. In this study, a hydrochemical investigation was conducted in the eastern coastal shallow aquifer of Laizhou Bay to identify the hydrochemical characteristics and the salinity of groundwater using ionic ratios, deficit or excess of each ions, saturation indices and factor analysis. The results indicate that groundwater in the study area showed wide ranges and high standard deviations for most of hydrochemical parameters and can be classified into two hydrochemical facies, Ca2+‐Mg2+‐Cl‐ facies and Na+‐Cl‐ facies. The ionic ratio, deficit or excess of each ions and SI were applied to evaluate hydrochemical processes. The results obtained indicate that the salinization processes in the coastal zones were inverse cation exchange, dissolution of calcite and dolomite, and intensive agricultural practices. Factor analysis shows that three factors were determined (Factor 1: TDS, EC, Cl‐, Mg2+, Na+, K+, Ca2+ and SO42‐; Factor 2: HCO3‐ and pH; Factor 3: NO3‐ and pH), representing the signature of seawater intrusion in the coastal zone, weathering of water–soil/rock interaction, and nitrate contamination, respectively. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
13.
This paper aims to identify the spatial distribution of exchangeable base cations in soils on an acid hillslope and to investigate possible cation release processes from slope soils to the stream. The basic assumption underlying this research is that the amount of exchangeable cations in soils reflects the nutrient stores and cation leaching processes across the slope where vegetation and parent materials are similar. The distribution of exchangeable Ca2+, Mg2+, K+ and Na+ has been investigated on a three-dimensional hillslope on the Quantock Hills, Somerset, UK. A two-way ANOVA shows that soil depth is predominant in explaining the total variance of exchangeable bases, despite the steep slope gradient and clear podzolic catena development. Major nutrient base cations, such as Ca2+, Mg2+ and K+, display homogeneous topsoil storage right across the slope. This spatial pattern may indicate that the spatial distribution of major nutrient cations is tightly controlled by the soil–vegetation system in nutrient-poor heathland environments. Na+ is an exception to this vegetation-controlled spatial distribution, because of its small involvement in the soil–vegetation and soil exchangeable systems. In subsurface soils, cations liberated from the soil–vegetation system are subject to redistribution over the slope according to the hydrological flowpaths operating on the slope, with some eventually released into the stream. The saturated wedge developed at the base of the slope plays a key role in the storage and release processes of base cations from slope soils to the stream. Ca2+, Mg2+ and Na+ carried by throughflow are stored in the saturated wedge and gradually released into the stream at times of high flow. K+, however, shows an apparently different spatial behaviour, being deficient in the saturated wedge. Copyright © 1999 John Wiley & Sons, Ltd. 相似文献
14.
Acid‐neutralizing capacity (ANC) is an important index for streamwater acidification caused by external factors (i.e. chronic acid deposition) and internal factors such as soil acidification due to nitrification. In this study, the influence of forest clear‐cutting and subsequent regrowth on internal acidification was investigated in central Japan, where stream pH (near 7·0) and ANC (above 0·1 meq L?1) are high. pH, the concentrations of major cations (Na+, K+, Mg2+ and Ca2+), major anions (NO3?, Cl? and SO42?) and dissolved silica (Si), and ANC were measured in 33 watersheds of various stand ages, during 2002 to 2004. Only NO3? concentration decreased with stand age, whereas pH, ANC, and concentrations of the sum of base cations (BC) and Si were negatively correlated with the minimum elevation of the watershed. The correlation between the BC/Si ratio and minimum elevation suggested that factors contributing to acid neutralization changed at 1100 m above sea level. In watersheds at lower elevations (?1100 m), the relatively high contribution of soil water with longer soil contact times should result in higher ANC, and cation exchange reactions should be the dominant process for acid neutralization due to deposition of colluvial soils on the lower slope. In contrast, in higher‐elevation watersheds (≥1100 m), weathered residual soils are thin and the small contribution of deeper groundwater results in lower ANC. These results suggest that the local acid sensitivity is determined by the hydrological and geomorphologic factors generated by steep topography. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
15.
对柴达木盆地察尔汗盐湖区外围沙下盐湖的卤水及沉积进行了综合研究。沙下盐湖卤水化学组成与地表径流和开放性盐湖卤水之间存在明显的差异性,具有高Na++Cl-、低Mg2++Ca2++SO42-、贫K++CO32-+HCO3-等特征。沙下盐湖析盐层位含有新生矿物并夹带碎屑矿物,其盐类矿物组合为:石盐+羟氯镁铝石+光卤石。25℃等温蒸发相图表明,其卤水演化方向往光卤石析出区迁移,在穿越上覆盖层通道中卤水发生的物理化学反应与独特的沉积特征,可以作为继续寻找沙下盐湖的指导。 相似文献
16.
A mathematical model of the middle and high latitude ionosphere 总被引：5，自引：0，他引：5
R. W. Schunk 《Pure and Applied Geophysics》1988,127(2-3):255-303
17.
This paper presents a numerical model and results for the mid-latitude ionospheric profile below the peak of the F2-layer. The basis of the model is the solving of equations for four ionic species O+, NO+, O+2 and N+2, as well as the meta-stable O+(2D) and O+(2P). Diffusion and wind-induced drifts and 21 photo-chemical reactions are also taken into account. Neutral atmospheric density and temperature are derived from the MSIS86 model and solar extreme ultraviolate irradiance from the EUV91 model. In an effort to obtain a more realistic ionospheric profile, the key point at foF2 and hmF2 is fitted from the simulation to observations. The model also utilizes the vertical drifts derived from ionosonde data with the help of the Servo model. It is shown that the ionospheric height of peak can be reproduced more accurately under the derived vertical drifts from the Servo theory than with the HWM90 model. Results from the simulation are given for Wuchang (30.5°N, 114.4°E) and Wakkanai (45.6°N, 141.7°E), showing the profile changes with season and solar activity, and the E-F valley structure (the depth and the width). This simulation also reveals the importance of meta-stable ions and dynamical transport processes on the formation of the F1-ledge and F1-F2 valley. 相似文献
18.
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
19.
《Journal of Atmospheric and Solar》2007,69(16):2028-2047
It has been clearly established that there is a substantial outflow of ionospheric plasma from the Earth's ionosphere in both the northern and southern polar regions. The outflow consists of both light thermal ions (H+ and He+) and an array of energized ions (NO+, O2+, N2+, O+, N+, He+, and H+). If the outflow is driven by thermal pressure gradients in the ionosphere, the outflow is called the “classical” polar wind. On the other hand, if the outflow is driven by energization processes either in the auroral oval or at high altitudes in the polar cap, the outflow is called the “generalized” polar wind. In both cases, the field-aligned outflow occurs in conjunction with magnetospheric convection, which causes the plasma to drift into and out of the sunlit hemisphere, cusp, polar cap, nocturnal auroral oval, and main trough. Because the field-aligned and horizontal motion are both important, three-dimensional (3-D) time-dependent models of the ionosphere–polar wind system are needed to properly describe the flow. Also, as the plasma executes field-aligned and horizontal motion, charge exchange reactions of H+ and O+ with the background neutrals (H and O) act to produce low-energy neutrals that flow in all directions (the neutral polar wind). This review presents recent simulations of the “global” ionosphere–polar wind system, including the classical, generalized, and neutral polar winds. The emphasis is on displaying the 3-D and dynamical character of the polar wind. 相似文献
20.
Concentrations of major ions in surface waters of the rivers of Khara-Murin and Snezhnaya are compared based on data of many-year observations carried out in the 1950s and 2000s. The concentrations of HCO 3 ? , Cl?, Ca2+, Mg2+, Na+ + K+ are shown to be stable. A considerable increase in SO 4 ?2 concentration was revealed. 相似文献