Chloride cycling in two forested lake watersheds in the west-central adirondack mountains,New York,U.S.A.

The chemistry of precipitation, throughfall, soil water, ground water, and surface water was evaluated in two forested lake-watersheds over a 4-yr period to assess factors controlling Cl^? cycling. Results indicate that Cl^? cycling in these watersheds is more complex than the generally held view of the rapid transport of atmospherically derived Cl^? through the excosystem. The annual throughfall Cl^? flux for individual species in the northern hardwood forest was 2 to 5 times that of precipitation (56 eq ha^?1), whereas the Na⁺ throughfall flux, in general, was similar to the precipitation flux. Concentrations of soil-water Cl^? sampled from ceramic tension lysimeters at 20 cm below land surface generally exceeded the Na⁺ concentrations and averaged 31 μeq L^?1, the highest of any waters sampled in the watersheds, except throughfall under red spruce which averaged 34 μeq L^?1. Chloride was concentrated prior to storms and mobilized rapidly during storms as suggested by increases in streamwater Cl^? concentrations with increasing flow. Major sources of Cl^? in both watersheds are the forest floor and hornblende weathering in the soils and till. In the Panther Lake watershed, which contains mainly thick deposits of till (>3 m), hornblende weathering results in a net Cl^? flux 3 times greater than that in the Woods Lake watershed, which contains mainly thin deposits of till. The estimated accumulation rate of Cl^? in the biomass of the two watersheds was comparable to the precipitation Cl^? flux.     

Trends of bulk precipitation and Streamwater Chemistry in a Small Mountainous Watershed on the Shikoku Island of Japan

For this study, characteristics and trends of the chemical constituents in bulk precipitation and streamwater were observed in a small mountainous watershed on the Shikoku Island of Japan, which covered an area of 27.4 hectares. Bulk precipitation and streamwater chemistry data spans from May 1997 to October 2004, and January 1996 to October 2004, respectively. The data were tested for two types of trends: (1) a monotonic trend to determine if concentrations of the chemical constituents were generally decreasing, increasing, or stable during the study period, and (2) a step trend to determine if a change occurred following the December 1999-January 2000 forest thinning. Both parametric and non-parametric statistical analyses were carried out in this study. Although the study area is only 35 km away from the Pacific Ocean, bulk precipitation chemistry was also influenced by terrestrial sources to a large extent. Streamwater chemistry was influenced by bedrock weathering, which was dominated by Ca²⁺ and HCO_3?, and was not strongly related top recipitation chemistry.Non?parametric Seasonal Kendall Test(SKT)showedadeceasingtr end of Ca ₂₊ and anincreasing tr end of K ₊ in bulk precipitation.Despite the decreasing trend of Mg ₂₊, an increasing trend of pH was found in the stream water.Non?paramet ric Mann?Whit ney?Wilcoxon Rank Sum test showed statistically sign if icantin creases of NO _3? and Ca ₂₊ in stream water followed by a moderate thinning operation.     

Effects of Nitrogen Fertilization on Stream Chemistry of Japanese Forested Watersheds

Steam chemistry was investigated from May 1991 through April 1992 for 13 Japanese forested watersheds and from May 1990 through August 1994 for two of these watersheds. Nine watersheds were treated over different periods (1983–1991) with different amounts of N (nitrogen) fertilizer as urea and ammonium salts. Total N additions ranged from 20 to 375 kg ha^-1. There were no distinct seasonal differences in stream NO₃ ^- concentrations in either the treated or untreated watersheds, but concentrations tended to be somewhat higher during periods of high discharge. The annual average NO₃ ^- concentrations in streams had a significant, positive (p < 0.001, r = 0.84) relationship to the total amount of N applied from 1985–1991. The application of 330 kg N ha^-1 raised annual average stream NO₃ ^- concentration to about 300 μeq L^-1 compared to less than 160 μeq L^-1 in untreated watersheds. The concentrations of K⁺, Ca²⁺, and Mg2+ in stream water also increased in those watersheds with high rates of N fertilizer as a result of nitrification that increased the generation of the mobile nitrate anion. The lack of seasonality in stream NO₃ ^- concentrations and the large rates of N loss with N addition both suggest that these watersheds were ‘nitrogen saturated’     

Examination of the Dissolved Inorganic Nitrogen Budget in Three Experimental Microbasins with Contrasting Land Cover—A Mass Balance Approach

A long-term hydrological and water chemistry research was conducted in three experimental microbasins differing in land cover: (1) a purely agricultural fertilized microbasin, (2) a forested microbasin dominated by Carpinus betulus (European hornbeam), and (3) a forested microbasin dominated by Picea abies (L.) (Norway spruce). The dissolved inorganic nitrogen (DIN: NH ₄ ⁺ , NO ₂ ^? , NO ₃ ^? ) budget was examined for a period of 3 years (1991–1993). Mean annual loads of DIN along with sulfate SO ₄ ^2? and base cations Ca²⁺, Mg²⁺, Na⁺, K⁺, and HCO ₃ ^? were calculated from ion concentrations measured in stream water, open-area rainfall, throughfall (under tree canopy), and streamwater at the outlets from the microbasins. Comparison of the net imported/exported loads showed that the amount of NO ₃ ^? leached from the agricultural microbasin is ～3.7 times higher (43.57 kg ha^?1?a^?1) than that from the spruce dominated microbasin (11.86 kg ha^?1?a^?1), which is a markedly higher export of NO ₃ ^? compared to the hornbeam dominated site. Our analyses showed that land cover (tree species) and land use practices (fertilization in agriculture) may actively affect the retention and export of nutrients from the microbasins, and have a pronounce impact on the quality of streamwater. Sulfate export exceeded atmospheric rainfall inputs (measured as wet deposition) in all three microbasins, suggesting an additional dry depositions of SO ₄ ^2? and geologic weathering.     

Input-Output Budgets of Inorganic Nitrogen for 24 Forest Watersheds in the Northeastern United States: A Review

Input-output budgets for dissolved inorganic nitrogen (DIN) are summarized for 24 small watersheds at 15 locations in the northeasternUnited States. The study watersheds are completely forested, free of recent physical disturbances, and span a geographical region bounded by West Virginia on the south and west, and Maine on the north and east. Total N budgets are not presented; however, fluxes of inorganic N in precipitation and streamwater dominate inputs and outputs of N at these watersheds. The range in inputs of DIN in wet-only precipitation from nearby National Atmospheric Deposition Program (NADP) sites was 2.7 to 8.1 kg N ha^-1 yr^-1 (mean = 6.4 kg N ha^-1 yr^-1; median = 7.0 kg N ha^-1 yr^-1). Outputs of DIN in streamwater ranged from 0.1 to 5.7 kg N ha^-1 yr^-1 (mean = 2.0 kg N ha^-1 yr^-1; median = 1.7 kg N ha^-1 yr^-1). Precipitation inputs of DIN exceeded outputs in streamwater at all watersheds, with net retention of DIN ranging from 1.2 to 7.3 kg N ha^-1 yr^-1 (mean = 4.4 kg N ha^-1 yr^-1; median = 4.6 kg N ha^-1 yr^-1). Outputs of DIN in streamwater were predominantly NO₃-N (mean = 89%; median = 94%). Wet deposition of DIN was not significantly related to DIN outputs in streamwater for these watersheds. Watershed characteristics such as hydrology, vegetation type, and land-use history affect DIN losses and may mask any relationship between inputs and outputs. Consequently, these factors need to be included in the development of indices and simulation models for predicting 'nitrogen saturation' and other ecological processes.     

Trends of Major Inorganic Species at the Small Watershed Ecosystem in Northern Tama Hills, the Western Tokyo Metropolitan Area, Japan

Acid rain impacts on the small forested watershed in northern Tama Hills in the western Tokyo metropolitan area Japan were investigated by surveying the trends of major inorganic species in rain and spring water during the years from 1991 to 1997. The ecosystem had been stressed by the annual H⁺-deposition of around 0.43 kmol/ha. The spring water outflow corresponded to ca. 27% of the precipitation. Budgets for the precipitation input and spring water output gave good balance for Cl^?,?0.01 ±0.09 kmol/ha, net gains for H⁺, NO₃ ^? and SO₄ ^2?, and to the contrary, relatively large net losses for Na⁺, Mg²⁺, Ca²⁺, Si(as H₄SiO₄) and HCO₃ ^?, thus suggesting the dissolution of chemical weathered products of silicate minerals. Further, in spring water, some concentration relationships were found: CNa⁺ = 376.5?2.05CCl^? (R²=0.748), CNa⁺=12.69+0.5556CHCO₃ ^? (R²=0.872) and CH₄SiO₄=130.0 + 1.108CHCO₃ ^? (R²=0.816). Evidently, the spring water chemistry reflected probable geochemical changes in the soil layer of the watershed. Mass balance in the ecosystem and estimation of the spring water output of chemical weathered products were investigated     

Biotic and abiotic processes controlling water chemistry during snowmelt at rabbit ears pass,Rocky Mountains,Colorado, U.S.A.

The chemical composition of snowmelt, groundwater, and streamwater was monitored during the spring of 1991 and 1992 in a 200-ha subalpine catchment on the western flank of the Rocky Mountains near Steamboat Springs, Colorado. Most of the snowmelt occurred during a one-month period annually that began in mid-May 1991 and mid-April 1992. The average water quality characteristics of individual sampling sites (meltwater, streamwater, and groundwater) were similar in 1991 and 1992. The major ions in meltwater were differentially eluted from the snowpack, and meltwater was dominated by Ca²⁺, SO ₄ ^2? , and NO ₃ ^? . Groundwater and streamwater were dominated by weathering products, including Ca²⁺, HCO ₃ ^? (measured as alkalinity), and SiO₂, and their concentrations decreased as snowmelt progressed. One well had extremely high NO ₃ ^? . concentrations, which were balanced by Ca²⁺ concentrations. For this well, hydrogen ion was hypothesized to be generated from nitrification in overlying soils, and subsequently exchanged with other cations, particularly Ca²⁺. Solute concentrations in streamwater also decreased as snowmelt progressed. Variations in groundwater levels and solute concentrations indicate that most of the meltwater traveled through the surficial materials. A mass balance for 1992 indicated that the watershed retained H⁺, NH ₄ ⁺ , NO ₃ ^? , SO ₄ ^2? and Cl^? and was the primary source of base cations and other weathering products. Proportionally more SO ₄ ^2? was deposited with the unusually high summer rainfall in 1992 compared to that released from snowmelt, whereas NO ₃ ^? was higher in snowmelt and Cl^? was the same. The sum of snowmelt and rainfall could account for greater than 90% of the H⁺ and NH ₄ ⁺ retained by the watershed and greater than 50% of the NO ₃ ^? .     

Three-component model of runoff generation,Lysina catchment,Czech Republic

The forested Lysina catchment is situated in an area very susceptible to acid deposition. The stream water is characterized by extremely high concentrations of total dissolved Al (volume weighted mean 66 Μmol L^?1) and H⁺ (average pH=3.87). In a simple two-component model, the surface runoff component contributes only 6% of runoff in winter and 4% of runoff in summer. During flood episodes, the direct runoff contributes up to 20% of streamflow. There is a strong positive correlation between stream acidity and stream discharge. The observed exponential increase in streamwater acidity with discharge during high flow periods cannot be explained by the simple two-component model. A three-component model used for hydrograph separation is based on chemical and¹⁸O analysis of precipitation, soil water and runoff. It incorporates a soil water component along with groundwater and rainfall components in streamwater generation. Dissociated organic acids leached during the flow of water through the uppermost soil horizon help to balance an apparent anion deficit. The apparent anion deficit was found to increase exponentially with flow rate. Low variability in streamwaterδ ¹⁸O corresponds to a high contribution of indirect components (i.e., soil and ground water) in the runoff. The soil water contribution to indirect runoff calculated from the apparent anion deficit of streamwater, varied from 0 at base flow up to 80% during floods. On average, 40% of the streamwater is derived from soil water (from 31 to 39% in winter and from 47 to 54% in summer).     

Seasonal mass balance of major ions in three small watersheds in a maritime environment

Three watersheds (16.4, 544, and 83 ha) at distances of 0.5, 20, and 40 km from the Atlantic coast have been monitored for major ion chemistry of precipitation input and streamflow from May 1977 to November 1978. More than 200 precipitation and stramflow samples were analyzed for Na, K, Ca, Mg, chloride and sulphate, as well as pH, conductivity, alkalinity, and compared to similar studies at Hubbard Brook, New Hampshire, U.S.A., and Kejimkujik National Park, Nova Scotia. Major ion chemistry reflects proximity to Atlantic and Bay of Fundy coastal sources of marine aerosols. Evidence is presented implying biological reduction of H ⁺ and S04 to H₂S during summer months for two consecutive growing seasons. Weighted mean annual pH values of precipitation for the three watersheds in Nova Scotia range from 4.11 to 4.63. More than 50% of the H ⁺ in precipitation is retained in the watersheds (with the exception of the ombrotrophic Fink Cove ecosystem), principally at the expense of basic cations being leached from the watersheds. Acidic deposition of Nova Scotian precipitation is predominantly as sulphuric acid, in contrast to ammonium sulphate, characteristic of continental precipitation.     

Acid-base chemistry of high-elevation streams in the great smoky mountains

Longitudinal and temporal variations in water chemistry were measured in several low-order, high-elevation streams in the Great Smoky Mountains to evaluate the processes responsible for the acid-base chemistry. The streams ranged in average base flow ANC from ?30 to 28 μeq L^?1 and in pH from 4.54 to 6.40. Low-ANC streams had lower base cation concentrations and higher acid anion concentrations than did the high-ANC streams. NO₃ ^? and SO₄ ^2? were the dominant acid anions. NO₃ ^? was derived from a combination of high leaching of nitrogen from old-growth forests and from high rates of atmospheric deposition. Streamwater SO₄ ^2? was attributed to atmospheric deposition and an internal bedrock source of sulfur (pyrite). Although dissolved Al concentrations increased with decreasing pH in the study streams, the concentrations of inorganic monomeric Al did not follow the pattern expected from equilibrium with aluminum trihydroxide or aluminum silicate phases. During storm events, pH and ANC declined by as much as 0.5 units and 15 μeq L^?1, respectively, at the downstream sites. The causes of the episodic acidification were increases in SO₄ ^2? and DOC.     

Chemical composition of precipitation in a forest area of Chongqing,Southwest China

Experiments were carried.out in Chongging-a city seriously damaged by acid precipitation in southwest China — to explore chemical compositions of open bulk precipitation, throughfall and stemflow in a Masson pine (Pinus massoniana) forest. The results showed that annual mean pH values of and annual ion depositions in the three types of rain water were 4.47 and 50.6 g m^?2, 3.82 and 69.7 g m^?2, and 2.92 and 0.215 g m^?2 respectively. pH values demonstrated an obvious seasonal variation; they were lower in winter than in the rest of the year. Ca²⁺ and NH _inf4 ^sup+ together made up more than 80% of the total cation, while SO _in4 ^sup2? alone contributed over 90% to the total anion. This high level of SO _in4 ^sup2? in rain water in Chongqing, which outran those found in other cities in China, was closely related to the combustion of locally produced coal that contains 3 to 5% sulphur. Thus, acid precipitation in Chongqing is of a typical sulphuric-acid type.     

Comparative Evaluation on Nitrogen Saturation of Forest Catchments in Japan and Northeastern United States

To analyze the differences in the status and processes of nitrogen saturation in Japan and northeastern United States, we examined the hydrobiogeochemistry of nitrogen of forested watersheds in these regions. Two distinct differences were found between watersheds in Japan compared with those in US. 1) In Japanese watersheds, marked decreases of NO₃ ^? concentration in surface waters during the summer growing season were not found and NO₃ ^? concentrations sometimes increased especially in the summer at nitrogen saturated sites. This contrast with watersheds in US where decreases in NO₃ ^? concentration during the summer are commonly observed except those watersheds in advanced stages of nitrogen saturation. These differences in NO₃ ^? concentration relationships can be attributed to climatic differences, with Japan having high precipitation and high discharge during the summer, while in many regions of North America lowest discharges are found in the summer. The climatic regime in Japan leads to high rates of mineralization and the rapid transport of NO₃ ^? to streams in summer. 2) Japanese watersheds, even those with high NO₃ ^? concentrations in surface waters, show little evidence of acidification. This is in contrast to sites in US where increased NO₃ ^? concentrations, especially during episodic events, result in surface water acidification.     

Niederschlags-Chemismus und atmosphärische Element-Deposition in einem an der Nordseeküste von Schleswig-Holstein gelegenen Agrarökosystem

Precipitation chemistry and atmospheric element-deposition in an agroecosystem at the North-Sea Coast of Schleswig-Holstein The objective of this study was to examine the chemistry of bulk precipitation and atmospheric element inputs in an arable soil near the North Sea coast of Schleswig-Holstein, North Germany. Bulk precipitation was collected at weekly intervals from November 1989 to October 1991. Precipitation amount, pH, electrical conductivity, and concentrations of Na⁺, K⁺, NH₄⁺, Mg²⁺, Ca²⁺, Cl^?, NO₃^?, and SO₄^2? were recorded. The average volume-weighted pH was 5.5 and the average EC was 92 μS cm^?1. Sodium and Cl^? were with 64% and 76% the dominant ions (equivalent concentration) in bulk precipitation indicating the influence of the North Sea. The contribution of marine alkalinity to neutralization reactions of bulk precipitation was negligible (1%). The neutralizing substances NH₃ (63%) and Carbonate (36%) were more important. Deposition rates were in 1990 and 1991 97.0 and 51.7 kg Na⁺ ha^?1, 6.2 and 4.0 kg K⁺ ha^?1, 15.0 and 8.4 kg Mg²⁺ ha^?1, 13.2 and 10.4 kg Ca²⁺ ha^?1, 12.3 and 9.5 kg NH₄⁺-N ha^?1, 8.0 and 5.9 kg NO₃^?-N ha^?1, 168 and 83.1 kg Cl^? ha^?1 and 19.1 and 12.7 kg SO₄^2?-S ha^?1. In 1990 both more westerly winds and stronger wind-forces occurred than in 1991 and resulted in higher inputs of marine origin. Calculated on Cl^? basis 93% of Na⁺, 55% of K⁺, 74% of Mg²⁺, 24% of Ca²⁺, and 36% of SO₄^2? were of marine origin. Atmospheric input of marine origin supplied 39–72% of Mg and 21–37% of S requirement for crop production. The North Sea is an important source providing significant amounts of these elements to agricultural crops.     

Fog and Precipitation Chemistry at Mt. Rokko in Kobe, April 1997-March 1998

Fog water and precipitation were collected and analyzed to study fog and precipitation chemistry. The research was carried out through one year from April 1997 to March 1998 at Mt. Rokko in Kobe. Higher fog occurrence and larger volume of fog water were observed in summer, corresponding to the trend of seasonal variation in precipitation amount. The annual mean pH value of fog water (3.80) was lower by ca. one pH unit than that of precipitation (4.74). The concentration of chemical species in fog water was ca. 7 times that in precipitation. The highest anion and cation concentrations were SO₄ ^2? and NH₄ ⁺ in fog water and Cl^? and Na⁺ in precipitation, although the Cl^?/Na⁺ equivalent ratio in both fog water and precipitation was almost the same value as that in sea water. It is considered that in the longest fog event, NH₄ ⁺ and nss-SO₄ ^2? in fog water mainly scavenged as (NH₄)₂SO₄, mainly derived from (NH₄)₂SO₄ (aerosol) in the atmosphere, NH₃ was scavenged at the growing stage, and SO₂ was also scavenged after the mature stage. NO₃ ^? in this fog event was mainly absorbed as HNO₃.     

Chemical Composition of Precipitation, Throughfall and Soil Solutions at Two Forested Sites in Guangzhou, South China

Rain water at two forested sites in Guangzhou (south China) show high concentrations of SO₄ ^2?, NO₃ ^? and Ca²⁺ and display a remarkable seasonal variation, with acid rain being more important during the spring and summer than during the autumn and winter. The amount of acid rain represents about 95% of total precipitation. The sources of pollutants from which acid rain developed includes both locally derived and long-middle distance transferred atmosphere pollutants. The seasonal variation in precipitation chemistry was largely related to the increasing neutralizing capacity of base cations in rainwater in winter. Soil acidification is highlighted by high H⁺ and Al³⁺ concentrations in soil solutions. The variation in elemental concentration in soil solution was related to nitrification (H⁺, NH₄ ⁺ and NO₃ ^?) and cation exchange reaction (H⁺, Al³⁺) in soil. The negative effect of soil acidification is partly dampened by substantial deposition of base cations (Ca²⁺, Mg²⁺ and K⁺) in this area.     

Patterns of nitrate loss from a chronosequence of clear-cut watersheds

Three clear-cuts at the Hubbard Brook Experimental Forest (NH) have resulted in a chronosequence of forest watersheds in close proximity. Following clear-cutting, the stands, now 12, 21, 27, and 78 years old, have different species composition, nutrient capital, and biogeochemistry. In this study, we compared seasonal patterns of NO₃ ^– in streamwater, changes in N capital, and N retention in watersheds of differing stand age. All of the watersheds showed elevated losses of NO₃ ^–, H⁺ and nutrient cations (Ca²⁺, Mg²⁺, K⁺) during the first few years following clear-cutting. Increased retention of N occurred during vegetation regrowth compared to the reference watershed (W6). Nitrate concentrations were low during the summer growing season, increased in the late fall and peaked in March during spring snowmelt. Concentrations of NO₃ ^– were lower in the regrowing watersheds than in W6 during all months. In W6, there was considerable year-to-year variability in N retention, which was not initially observed in the manipulated watersheds. However, two cut watersheds exhibited higher export of NO₃ ^– in 1989 and 1990, corresponding to a 10-year high value in annual NO₃ ^– loss in W6. These results demonstrate the importance of land use and cutting history in assessments of N saturation and loss from forest watersheds.     

Fog- and Rainwater Chemistry in the Tropical Seasonal Rain Forest of Xishuangbanna, Southwest China

Fogwater, fog drip and rainwater chemistry were examined at a tropical seasonal rain forest in Xishuangbanna, southwest China between November 2001 and October 2002. During the period of observation, 204 days with the occurrence of radiation fog were observed and the total duration of fog was 1949 h, of which 1618 h occurred in the dry season (November to April), accounting for 37.0% of the time during the season. The mean pH of fogwater, fog drip and rainwater were 6.78, 7.30, and 6.13, respectively. The ion with the highest concentration for fog- and rainwater was HCO₃ ^?, which amounted to 85.2 and 37.3 μeq l^?1, followed by Ca²⁺, Mg²⁺ and NH₄ ⁺. Concentrations of NO₃ ^?, HCO₃ ^?, NH₄ ⁺, Ca²⁺, and K⁺ in fogwater samples collected in the dry season were significantly greater when compared to those collected in the rainy season. It was found that the ionic concentrations in fog drip were higher than those in fogwater, except for NH₄ ⁺ and H⁺, which was attributed to the washout of the soil- and ash-oriented ions deposited on the leaves and the alkaline ionic emissions by the leaves, since biomass burns are very common in the region and nearby road was widening.     

Hydrogen ion input to the hubbard brook experimental forest,New Hampshire,during the last decade

Being downwind of eastern and midwestern industrial centers, the Hubbard Brook Experimental Forest offers a prime location to monitor long-term trends in atmospheric chemistry. Continuous measurements of precipitation chemistry during the last 10 yr provide a measure of recent changes in precipitation inputs of H ion. The weighted average pH of precipitation during 1964–65 to 1973–74 was 4.14, with a minimum annual value of 4.03 in 1970–71 and a maximum annual value of 4.21 in 1973–74. The sum of all cations except H ion decreased from 51 μeq 1^?1 in 1964–65 to 23 μeq 1^?1 in 1973–74 providing a significant drop in neutralizing capacity during this period. Based upon regression analysis, the input in equivalents of H ion and nitrate increased by 1.4-fold and 2.3-fold respectively, from 1964–65 to 1973–74. Input of all other ions either decreased or showed no trend. Based upon a stoichiometric formation process in which a sea-salt, anionic component is subtracted from the total anions in precipitation, SO₄ ⁼, contribution to acidity dropped from 83% to 66%, whereas NO₃ ^? increased from 15% to 30% during 1964–65 to 1973–74. The increased annual input of H ion at Hubbard Brook during the past 10 yr is highly correlated with the increased input of nitrate in precipitation.     

新疆伊犁察南灌区土壤盐分特征

以察南灌区土壤为研究对象,对不同含盐量土壤进行盐化程度分级,并对该地区土壤盐分特征进行相关分析和主成分分析,以及对土壤盐分因子区域影响因素进行探讨。结果表明:察南灌区以碱性土壤为主,HCO_3~–是影响该灌区土壤p H最强的因子;对灌区0~100 cm土体土壤的分析表明,灌区盐化土面积约为总灌溉面积的1/4,盐渍化风险较大;相关性分析显示,HCO–3、Cl~–、SO_4~(2-)、Ca~(2~+)、Mg~(2~+)、Na~+、K~+为盐分主要组成离子,总盐分与各离子之间均呈正相关关系,与总盐分相关性最强的阴离子为SO_4~(2-),相关性最强的阳离子为Mg~(2~+);主成分分析显示,HCO_3~–、Cl~–、K~+为影响该灌区土壤盐分特征的主导因子;通过盐分因子区域影响因素定性分析可知,除HCO_3~–和pH是由河流以及地下水综合作用影响外,其他盐分因子均主要受河流影响。     

Contribution of dissolved organic nitrogen deposition to nitrogen saturation in a forested mountainous watershed in Tsukui, Central Japan

Nitrogen (N) budget was estimated with dissolved inorganic N (DIN) and dissolved organic N (DON) in a forested mountainous watershed in Tsukui, Kanagawa Prefecture, about 50 km west of Tokyo in Central Japan. The forest vegetation in the watershed was dominant by Konara oak (Quercus serrata) and Korean hornbeam (Carpinus tschonoskii), and Japanese cedar (Cryptomeria japonica). Nitrate (NO₃ ^?) concentration in the watershed streamwater was averagely high (98.0 ±± 19 (±± SD, n = 36) μmol L^?1) during 2001–2003. There was no seasonal and annual changes in the stream NO^? ₃ concentration even though the highest N uptake rate presumably occurred during the spring of plant growing season, a fact indicating that N availability was in excess of biotic demands. The DON deposition rates (DON input rates) in open area and forest area were estimated as one of the main N sources, accounting for about 32% of total dissolved N (TDN). It was estimated that a part of the DON input rate contributed to the excessive stream NO^? ₃ output rate under the condition of the rapid mineralization and nitrification rates, which annual DON deposition rates were positively correlated with the stream NO₃ ^? output rates. The DON retention rate in the DON budget had a potential capacity, which contributed to the excessive stream NO^? ₃ output rate without other N contributions (e.g. forest floor N or soil N).