Effects of a clearcut on the net rates of nitrification and N mineralization in a northern hardwood forest,Catskill Mountains,New York,USA

The Catskill Mountains of southeastern New York receive among the highest rates of atmospheric nitrogen (N) deposition in eastern North America, and ecosystems in the region may be sensitive to human disturbances that affect the N cycle. We studied the effects of a clearcut in a northern hardwood forest within a 24-ha Catskill watershed on the net rates of N mineralization and nitrification in soil plots during 6 years (1994–1999) that encompassed 3-year pre- and post-harvesting periods. Despite stream NO₃^– concentrations that increased by more than 1400 mol l^–1 within 5 months after the clearcut, and three measures of NO₃^– availability in soil that increased 6- to 8-fold during the 1^st year after harvest, the net rates of N mineralization and nitrification as measured by in situ incubation in the soil remained unchanged. The net N-mineralization rate in O-horizon soil was 1– 2 mg N kg^–1 day^–1 and the net nitrification rate was about 1 mg N kg^–1 day^–1, and rates in B-horizon soil were only one-fifth to one-tenth those of the O-horizon. These rates were obtained in single 625 m² plots in the clearcut watershed and reference area, and were confirmed by rate measurements at 6 plots in 1999 that showed little difference in N-mineralization and nitrification rates between the treatment and reference areas. Soil temperature increased 1 ± 0.8 °C in a clearcut study plot relative to a reference plot during the post-harvest period, and soil moisture in the clearcut plot was indistinguishable from that in the reference plot. These results are contrary to the initial hypothesis that the clearcut would cause net rates of these N-cycling processes to increase sharply. The in situ incubation method used in this study isolated the samples from ambient roots and thereby prevented plant N uptake; therefore, the increases in stream NO₃^– concentrations and export following harvest largely reflect diminished uptake. Changes in temperature and moisture after the clearcut were insufficient to measurably affect the net rates of N mineralization and nitrification in the absence of plant uptake. Soil acidification resulting from the harvest may have acted in part to inhibit the rates of these processes. The US Governments right to retain a non-exclusive, royalty-free license in and to any copyright is acknowledged.     

Effects of forest clear-cutting on the sulphur, phosphorus and base cations fluxes through podzolic soil horizons

Clear-cutting considerably alters the flow of nutrients through the forest ecosystem. These changes are reflected in soil solution concentrations and fluxes. The effects of clear-cutting (stems only) on the fluxes of water soluble phosphorus (P), sulphur (S) and base cations (Ca, Mg and K) through a podzolic soil were studied in a Norway spruce dominated mixed boreal forest in eastern Finland. Bulk deposition, total throughfall (throughfall + stemflow) and soil percolate from below the organic (O), eluvial (E) and illuvial (B) horizons were collected for 4 years before and for 3 years after cutting. Annual deposition loads (kg ha^–1) to the forest floor were less after clear-cutting, averaging 1.7 S, 0.84 Ca, 0.14 Mg, 0.64 K and 0.10 P. Before cutting, the loads were 4.6 S, 2.7 Ca, 0.70 Mg, 6.2 K and 0.20 P. Annual fluxes of total S and sulphate (SO ₄ ^2– ) from below the O-horizon were also lower (33%) after clear-cutting, total S averaging 2.0 kg ha^–1, the flux from below the B-horizon also diminished after clear-cutting. The flux of total P (mainly inorganic) from below the O-horizon increased threefold (6.9 kg ha^–1; sum over the 3-year period) compared to period before cutting. The fluxes of base cations from below the O-horizon increased twofold. The flux of K⁺ from below the O- and E-horizons was most strongly correlated with that of phosphate (PO ₄ ^3– ) and those of Ca²⁺ and Mg²⁺ with the DOC flux. Increased fluxes of P and base cations to the mineral soil generated only slightly increased fluxes from below the B-horizon. The retention of base cations and P in the mineral soil indicates there was little change in leaching to ground and surface waters after clear-cutting.     

Spatial variability of throughfall chemistry and selected soil properties as influenced by stem distance in a mature Norway spruce (Picea abies,Karst.) stand

Our aims were to investigate the spatial variability of throughfall chemistry and soil parameters as influenced by stem distance and to evaluate the implication of the observed systematic and random patterns for the sampling strategy.One hundred throughfall samplers with a sampling area of 106 cm² each were established in a systematic grid around 5 trees in a mature Norway spruce; site of the Fichtelgebirge (Germany). One hundred soil cores were taken with an auger of 50 cm² next to the throughfall samplers. Soil samples were stratified according to genetic soil horizons and analysed for pH, exchangeable NH₄ ⁺, SO₄ ^2– and total-S. Throughfall samples were collected over a period of 6 months. For each sampler an aliquod sample was mixed over the observation period and analysed for major ions.The spatial variability of the element concentrations in throughfall, expressed by the coefficient of variance, was 21–164%, depending on the element considered. For precipitation volume, the coefficient of variance was only 3%. The distance to the stem influenced most element concentrations in throughfall with increasing concentrations approaching the stem. Steepest gradients were observed in case of SO₄ ^2– and H⁺.The spatial variability of the investigated soil parameters was also very high with the exception of pH. The SO₄ ^2– content of the forest floor reflected the gradients observed in throughfall, while for the other investigated soil parameters and soil horizons no significant relations to stem distance were found.To determine site representative throughfall concentrations and soil properties with the sample volumes and time intervals we used, the number of samples required to get a statistical error of less than 10% (with 95% probability) can be very high. In case of throughfall, more than 100, and in case of the soil parameters, more than 300 replicates would be required.     

Solution chemistry profiles of mixed-conifer forests before and after fire

Solution chemistry profiles of mixed-conifer forests in granitic catchments of the Sierra Nevada were measured for three years before (1987–1990) and three years after (1990–1993) prescribed fire. Wet deposition, throughfall and soil solution samplers were installed in both white-fir and giant-sequoia dominated forest stands underlain by poorly developed inceptisols. Stream water chemistry was monitored as part of an ongoing study of catchment outputs. Calcium, NO ₃ ^– and Cl^– were the major ions in precipitation. Canopy leaching increased mean concentrations of all major ions, especially K⁺ and Ca²⁺. Water flux through the soil occurred largely during spring snowmelt. Forest floor leachate represented the most concentrated solutions of major ions. Interaction with the mineral soil decreased mean concentrations of most species and the average composition of soil solutions closely resembled stream water at baseflow. Bicarbonate alkalinity, Ca²⁺, Mg²⁺, and Na⁺ were enriched in stream water relative to precipitation whereas inputs of H⁺, NH ₄ ⁺ , NO ₃ ^– and SO ₄ ^2– were retained within the catchments.Burning of the forest understory and litter layer increased solute concentrations in soil solution and stream water. Mean soil solution Ca²⁺, Mg²⁺ and K⁺ concentrations increased more than 10 fold, but the relative predominance of these cations was not affected by burning. Sulfate concentration, which was very low in soil solutions of undisturbed stands (<25 mmol_c m^–3), increased more than 100 times following fire. Ammonium concentration exhibited a rapid, short-term increase and then a decrease below pre-burn levels. Changes in soil solution chemistry were reflected in catchment outputs.Corresponding author.     

Longitudinal and seasonal patterns of stream acidity in a headwater catchment on the Appalachian Plateau, West Virginia, U.S.A.

The chemical composition during baseflow was used to elucidate the fundamental processes controlling longitudinal and seasonal patterns of stream acidity in Yellow Creek, a chronically acidic headwater (pH range 3.7--4.2) on the Appalachian Plateau in northeastern West Virginia. Sulfate concentrations controlled the variability of stream acidity within the Yellow Creek catchment. Decreases in stream free H⁺ acidity with decreasing elevation likely resulted from SO ₄ ^2– retention in riparian wetland areas as well as spatial variation in dominant tree species. Seasonal variations in free H⁺ and inorganic monomeric aluminum (Alⁿ⁺) concentrations appeared related to seasonal fluctuations in baseflow discharge which was controlled by vegetative activity. Baseflow stream discharge, as well as H⁺ and Alⁿ⁺ acidity, gradually declined during the growing season (June through October), likely reflecting microbial SO ₄ ^2– > reduction in saturated anaerobic environments within riparian wetlands. A marked pulse of stream H⁺, Alⁿ⁺, and SO ₄ ^2– coincided with an abrupt increase in baseflow discharge resulting from the cessation of transpiration after leaf-fall in November. This seasonal pattern suggests that autumn may be a critical period for eastern brook trout in streams draining wetlands on the Appalachian Plateau.     

The biogeochemistry of potassium at Hubbard Brook

A synthesis of the biogeochemistry of K was conducted during 1963–1992 in the reference and human-manipulated watershed-ecosystems of the Hubbard Brook Experimental Forest (HBEF), NH. Results showed that during the first two years of the study (1963–65), which coincided with a drought period, the reference watershed was a net sink for atmospheric inputs of K. During the remaining years, this watershed has been a net source of K for downstream ecosystems. There have been long-term declines in volume-weighted concentration and flux of K at the HBEF; however, this pattern appears to be controlled by the relatively large inputs during the initial drought years. Net ecosystem loss (atmospheric deposition minus stream outflow) showed an increasing trend of net loss, peaking during the mid-1970s and declining thereafter. This pattern of net K loss coincides with trends in the drainage efflux of SO₄ ^2– and NO₃ ^–, indicating that concentrations of strong acid anions may be important controls of dissolved K loss from the site. There were no long-term trends in streamwater concentration or flux of K. A distinct pattern in pools and fluxes of K was evident based on biotic controls in the upper ecosystem strata (canopy, boles, forest floor) and abiotic controls in lower strata of the ecosystem (mineral soil, glacial till). This biological control was manifested through higher concentrations and fluxes of K in vegetation, aboveground litter, throughfall and forest floor pools and soil water in the northern hardwood vegetation within the lower reaches of the watershedecosystem, when compared with patterns in the high-elevation spruce-fir zone. Abiotic control mechanisms were evident through longitudinal variations in soil cation exchange capacity (related to soil organic matter) and soil/till depth, and temporal and disturbance-related variations in inputs of strong-acid anions. Marked differences in the K cycle were evident at the HBEF for the periods 1964–69 and 1987–92. These changes included decreases in biomass storage, net mineralization and throughfall fluxes and increased resorption in the latter period. These patterns seem to reflect an ecosystem response to decreasing rates of biomass accretion during the study. Clearcutting disturbance resulted in large losses of K in stream water and from the removal of harvest products. Stream losses occur from release from slash, decomposition of soil organic matter and displacement from cation exchange sites. Elevated concentrations of K persist in stream water for many years after clearcutting. Of the major elements, K shows the slowest recovery from clearcutting disturbance.     

Change in water quality during the passage through a tropical montane rain forest in Ecuador

We studied five 20-m transects onthe lower slope under tropical lower montanerain forest at 1900–2200 m above sea level. We collectedsamples of soil and of weekly rainfall,throughfall, litter leachate, and stream waterbetween 14 March 1998 and 30 April 1999 anddetermined the concentrations of Al, totalorganic C (TOC), Ca, Cl^–, Cu, K, Mg, Mn,NH₄ ⁺-N, NO₃ ^–-N, total N (TN), Na, P, S, and Zn. The soils were shallowInceptisols; pH ranged 4.4–6.3 in the Ohorizons and 3.9–5.3 in the A horizons, totalCa (6.3–19.3 mg kg^–1) and Mgconcentrations (1.4–5.4) in the O horizon weresignificantly different between the transects.Annual rainfall was 2193 mm; throughfall variedbetween 43 and 91% of rainfall, cloud waterinputs were 3.3 mm a^–1 except forone transect (203). The volume-weighted mean pHwas 5.3 in rainfall and 6.1–6.7 in throughfall.The median of the pH of litter leachate andstream water was 4.8–6.8 and 6.8, respectively.The concentrations of Ca and Mg in litterleachate and throughfall correlatedsignificantly with those in the soil (r =0.76–0.95). Element concentrations inthroughfall were larger than in rainfallbecause of leaching from the leaves (Al, TOC,Ca, K, Mg), particulate dry deposition (TOC,Cu, Cl^–, NH₄ ⁺-N), and gaseousdry deposition (NO₃ ^–-N, total N, S).Net throughfall (= throughfall-rainfalldeposition) was positive for most elementsexcept for Mn, Na, and Zn. High-flow eventswere associated with elevated Al, TOC, Cu, Mn,and Zn concentrations.     

Mineral nitrogen and microbial dynamics in the forest floor of clearcut or partially harvested successional boreal forest stands

The effects of clearcut and partial harvesting of early-seral trembling aspen plots were compared to conventional clearcut harvesting in mid-seral mixedwood and late-seral conifer plots. Twice a year, for three consecutive years, we assessed mineral N and microbial dynamics in the forest floor of these plots to test three hypotheses related to the higher litter quality of aspen leaves and to the sustained inputs of available C on partially harvested plots: (1) the post-clearcutting mineral N flush and the net [(NO₃^–): (NO₃^– + NH₄⁺)] production ratio (RNI) are higher in aspen plots than in black spruce plots, with intermediate values occurring in mixedwood plots; (2) net N mineralization rates in aspen plots are higher in spring than in autumn; and (3) compared to clearcutting, partial harvesting reduces potential ammonification and nitrification rates. Initial NH₄⁺ and NO₃^– concentrations respectively ranged between 1.7–4.4 and 0.2–1.5 g N kg^–1 N_total, net ammonification and nitrification rates (30 d incubations) respectively ranged between 5.3–17.8 and 0.1–27.6 g N kg^–1 N_total, basal respiration ranged between 20.9–38.9 mg CO₂-C kg^–1 h^–1, and microbial biomass ranged between 6.1–8.7 g C_mic kg^–1. Although clearcutting increased NO₃^– concentrations in aspen plots, the balance of our results did not support our first hypothesis, because NH₄⁺ concentrations increased in conifer plots only, potential ammonification was unaffected by clearcutting, potential nitrification increased in mixedwood plots only, and RNI increased in all plots. In each seral stage, basal respiration, microbial biomass, and metabolic quotient either increased or were unaffected by clearcutting, suggesting that increases in RNI after disturbance were not related to lower microbial immobilisation of NO₃^– due to lower available C. Forest floors in mid-seral mixedwood plots exhibited a distinct combination of mineral N and microbial properties, suggesting that the functional richness of the forest is enhanced not only by the number of species, but also by the diversity of assemblages that are present. Results supported our second hypothesis and showed, furthermore, that net N mineralization in conifer stands is greater in autumn than in spring. Partial harvesting in aspen stands resulted in lower potential mineralization of N and lower RNI, compared to clearcutting. Further lysimetry studies are needed to confirm whether partial harvesting mitigates NO₃^– leaching following disturbance.     

Processes regulating temporal and longitudinal variations in the chemistry of a low-order woodland stream in the Adirondack region of New York

Watershed processes influence the acid neutralizing capacity of surface waters by mediating changes in concentration of ionic solutes. Acidification of surface waters by atmospheric deposition of mineral acids and the extent to which ecosystem transformations neutralize this acidity are of particular concern. Seasonal variations in flow paths of water through soil and biological processes result in short-term changes in chemistry that may be critical to surface water ecology. In this study, we assessed longitudinal and temporal variations in the chemistry of a low-order stream, Pancake-Hall Creek, located in the west-central Adirondack region of New York. By quantifying changes in ionic solute concentration (e.g. Ca²⁺, Al^a+, SO ₄ ^2– , NO ₃ ^– ) we were able to evaluate processes responsible for short-term fluctuations in acid/base chemistry.In the headwater sites, stream water was acidic; changes in pH, acid neutralizing capacity (ANC) and Al were primarily due to seasonal variations in basic cation and NO ₃ ^– concentrations. At the downstream sites, water migrated through a large beaver impoundment and thick till resulting in higher pH, acid neutralizing capacity and basic cation concentrations, and lower concentrations of Al. Neutralization of acidity was particularly evident during the low flow summer period and coincided with retention of SO ₄ ^2– in the beaver impoundment. During the high flow non-summer (October to June) period, depressed pH and ANC, and elevated Al concentrations were observed in the downstream sites. Acidic conditions during the non-summer period were not due to the oxidation of reduced sulfur deposits (e.g. SO ₄ ^2– events) but rather the resumption of conservative SO ₄ ^2– transport through the beaver impoundment (e.g. minimal SO ₄ ^2– retention) coupled with increases in NO ₃ ^– .     

Patterns of stable S isotopes in a forested catchment as indicators for biological S turnover

Despite intensive biogeochemical research during the last thirty years, the relative importance of biological S turnover for the overall SO ₄ ^2– budget of forested catchments remains uncertain. The objective of the present study was (i) to gain new insight into the S cycle of theLehstenbach catchment (Northeastern Bavaria, Germany) through the analysis of stable isotopes of S and (ii) to differentiate between sites which are hot spots for SO ₄ ^2– reduction and sites where mineralization and adsorption/desorption processes are more important. The ³⁴S values and SO ₄ ^2– concentrations of soil solutions, throughfall and groundwater at four different sites as well as runoff of the catchment were measured. The relatively low variability of ³⁴S in throughfall and bulk precipitation was in contrast to the high temporal and spatial variability of ³⁴S in the soil solution. Sulfate in the soil solution of upland sites was slightly depleted in³⁴S compared to input values. This was most likely due to S mineralization. Sulfate in the soil solution from wetland soils was clearly enriched in³⁴S, indicating dissimilatory SO ₄ ^2– reduction. The observed spatial and temporal patterns of³⁴S turnover and SO ₄ ^2– concentrations might explain the overall balanced S budget of the catchment. At a time of decreasing anthropogenic deposition SO ₄ ^2– is currently released from upland soils. Furthermore, mineralization of organic S may contribute to SO ₄ ^2– release. Wetland soils in the catchment represent a sink for SO ₄ ^2– due to dissimilatory SO ₄ ^2– reduction.     

The effects of liming an Adirondack lake watershed on downstream water chemistry

Calcite treatment of chronically acidic lakes has improved fish habitat, but the effects on downstream water quality have not previously been examined. In this study, the spatial and temporal effects of watershed CaCO₃ treatment on the chemistry of a lake outlet stream in the Adirondack Mountains of New York were examined. Before CaCO₃ treatment, the stream was chronically acidic. During spring snowmelt before treatment, pH and acid-neutralizing capacity (ANC) in the outlet stream declined, and NO ₃ ^– and inorganic monomeric aluminum (Al_IM) concentrations increased sharply. During that summer, SO ₄ ^– and NO ₃ ^– concentrations decreased downstream, and dissolved organic carbon (DOC) concentrations and ANC increased, in association with the seasonal increase in decomposition of organic matter and the attendant SO ₄ ^– -reduction process. A charge-balance ANC calculation closely matched measured downstream changes in ANC in the summer and indicated that SO ₄ ^– reduction was the major process contributing to summer increases in ANC. Increases in Ca²⁺ concentration and ANC began immediately after CaCO₃ application, and within 3 months, exceeded their pretreatment values by more than 130 eq/L. Within 2 months after treatment, downstream decreases in Ca²⁺ concentration, ANC, and pH, were noted. Stream mass balances between the lake and the sampling site 1.5 km downstream revealed that the transport of all chemical constituents was dominated by conservative mixing with tributaries and ground water; however, non-conservative processes resulted in significant Ca²⁺ losses during the 13-month period after CaCO₃ treatment. Comparison of substrate samples from the buffered outlet stream with those from its untreated tributaries showed that the percentage of cation-exchange sites occupied by Ca²⁺ as well as non-exchangeable Ca, were higher in the outlet-stream substrate than in tributary-stream substrate. Mass-balance data for Ca²⁺ H⁺, Al_IM, and DOC revealed net downstream losses of these constituents and indicated that a reasonable set of hypothesized reactions involving Al_IM, HCO ₃ ^– , Ca²⁺, SO ₄ ^– NO ₃ ^– , and DOC could have caused the measured changes in stream acid/base chemistry. In the summer, the sharp decrease in ANC continued despite significant downstream decreases in SO₄ ^2– concentrations. After CaCO₃ treatment, reduction of SO ₄ ^– was only a minor contributor to ANC changes relative to those caused by Ca²⁺ dilution from acidic tributaries and acidic ground water, and Ca²⁺ interactions with stream substrate.     

Sources and sinks of dissolved organic carbon in a forested swamp catchment

Concentrations of dissolved organic carbon (DOC) were measured in precipitation, throughfall, stemflow, and soil, peat and stream water in a 50 ha catchment with a central 5 ha swamp at Mont St. Hilaire, Quebec. DOC concentrations in precipitation were low (2.0 mg L^–1), but increased in passage through the tree canopies as throughfall (9.1–14.6 mg L^–1) and stemflow (23.1–30.1 mg L^–1). For the period July 1–November 15, 1987, 0.5 g DOC m^–2 was imported as precipitation, and forest canopies contributed a further 1.4–1.7 g m^–2 2 to the soil surface. DOC concentrations were higher (46.0 and 67.6 mg L^–1) in upland soil organic horizons, but decreased with depth because subsoil mineral horizons acted as a major sink of DOC. A laboratory experiment using leaf leachate revealed that subsoil horizons were able to adsorb DOC, with equilibrium DOC concentrations ranging from 3 to 19 mg L^–1. Soil organic carbon appeared to be an important determinant of equilibrium DOC concentrations. The swamp was a major source of DOC, with an overall average DOC concentration of 58.6 mg L^–1 and showed strong spatial and temporal variations related to hydrologic and thermal regimes. During base flow periods, stream DOC concentrations were small (< 3 mg L^–1), dominated by water fed from springs draining upland soils. During high flows, stream DOC concentrations increased through the contribution of DOC-rich water originating in the swamp. Sources, sinks and transport of DOC are thus a function of a complex set of inter-related biotic and abiotic process.     

Nitrogen dynamics of storm runoff in the riparian zone of a forested watershed

The influence of storm runoff processes on stream nitrogen dynamics was investigated in a headwater riparian swamp on the Oak Ridges moraine in southern Ontario. Hydrologic data were combined with analysis of an isotopic tracer (¹⁸0) and nitrogen (NH ₄ ⁺ , NO ₃ ^– ) concentrations in saturation overland flow and stream discharge. Storm runoff was separated into its event and pre-event components using¹⁸O in order to examine the effect of water source on nitrogen chemistry. Laboratory experiments were also used to study nitrogen transformation associated with storm runoff-surface substrate interactions in the swamp. In most storms N0₃-N and NH₄-N concentrations in the initial 3–4 mm throughfall increment were 10–20x and 20–100x higher respectively than stream base flow concentrations. Maximum stream N0₃-N concentrations were < 2x to 6x higher than base flow concentrations and preceded or coincided with peak stream discharge. Storm-to-storm variations in stream N0₃-N behaviour also occurred during the hydrograph recession phase. NH₄-N concentrations attained an initial peak on the rising hydrograph limb, or at peak stream discharge. A second NH₄-N increase occurred during the late recession phase 3–5 h after maximum stream discharge. Inorganic-N concentrations in surface runoff were similar to peak streamflow.The close agreement between observed N0₃-N concentrations and values predicted from a chemical mixing model indicate that stream N0₃-N variations were controlled mainly by the mixture of throughfall and groundwater in surface stormflow from the swamp. Laboratory experiments also indicated that N0₃-N in surface runoff behaved conservatively when mixed with swamp substrates. With the exception of the late hydrograph recession phase, observed stream NH₄-N concentrations were much lower than concentrations predicted by the chemical mixing model. The rapid loss of NH₄-N from mixtures of surface stormflow and swamp substrates in laboratory experiments and the absence of uptake in sterilized substrates indicated that NH₄-N retention in surface storm runoff was due to biotic processes.     

Forest soil solutions: Acid/base chemistry and response to calcite treatment

Soil solution chemistry was investigated at a forested watershed draining into Woods Lake. N.Y. as part of the Experimental Watershed Liming Study (EWLS). The objective of this study was to assess the response of soil water to watershed treatment of calcite (CaCO₃). This material was applied in an effort to mitigate the effects of acidic atmospheric deposition. Soil solutions draining Oa and Bs horizons in reference subcatchments were characterized by low pH and acid neutralizing capacity (ANC) due to elevated concentrations of SO ₄ ^2– , NO ₃ ^– and organic anions relative to the sum of base cation (C_B Ca²⁺, Mg²⁺, Na⁺, K⁺) concentrations. Seasonal and spatial variation of pH andANC in soil solutions appeared to belargely controlled by variations in the concentrations of dissolved organic acids which, in turn, were regulated by reactions of Al with soil organic matter. Nitrate was positively correlated and SO²⁺ was negatively correlated with Ca²⁺ and Al concentrations in reference soil solutions, indicating that changes in NO ₃ ^– influences spatial and seasonal variations in Ca²⁺ and Al concentrations. On this basis, NO ₃ ^– appears to be important in soil acidification and the dynamics of drainage water acidity. Comparison of our results with historical data for the site showed declines in concentrations of SO ₄ ^2– , which are consistent with decreases in emissions of SO₄, in the eastern U.S. and atmospheric deposition of SO ₄ ^2– , to the Adirondack region. Mineral soil solutions have shown large increases in concentrations of NO ₃ ^– . Declines in concentrations of C_B and increases in concentrations of Al have occurred over the last ten years, suggesting depletion of soil pools of exchangeable basic cations and increased sensitivity to acidic deposition. Calcite (CaCO₃) treatment of 6.89 Mg/ha resulted in a significant increase of Ca²⁺, ANC and pH in both Oa and Bs horizon soil solutions. Soil water response to CaCO₃ addition was most evident during the first year after treatment, apparently due to macropore transport of particulate and dissolved CaCO₃ However, increases in ANC and pH in the mineral soil waters were not sustained and appeared insufficient to result in substantial improvement in surface water quality over the 43 month study period.     

Controls on the dynamics of dissolved organic carbon and nitrogen in a Central European deciduous forest

Despite growing attention concerning therole of dissolved organic matter (DOM) inelement cycling of forest ecosystems, thecontrols of concentrations and fluxes of bothdissolved organic carbon (DOC) and nitrogen(DON) under field conditions in forest soilsremain only poorly understood. The goal ofthis project is to measure the concentrations and fluxes of DON, NH₄ ⁺, NO₃ ^–and DOC in bulkprecipitation, throughfall, forest floorleachates and soil solutions of a deciduousstand in the Steigerwald region (northernBavaria, Germany). The DOC and DONconcentrations and fluxes were highest inleachates originating from the Oa layer of theforest floor (73 mg C L^–1, 2.3 mg NL^–1 and about 200–350 kg C, 8–10 kg Nha^–1 yr^–1). They were observed to behighly variable over time and decreased in themineral topsoil (17 mg C L^–1, 0.6 mg NL^–1 and about 50–90 kg C, 2.0 to 2.4 kg Nha^–1 yr^–1). The annual variability ofDOC and DON concentrations and subsequentialDOC/DON ratios was substantial in allsolutions. The DOC and DON concentrations inthroughfall were positively correlated withtemperature. The DOC and DON concentrationsdid not show seasonality in the forest floorand mineral soil. Concentrations were notrelated to litterfall dynamics but didcorrespond in part to the input of DOC and DONfrom throughfall. The throughfall contributionto the overall element fluxes was higher forDON than for DOC. Concentrations and fluxes ofDON were significantly correlated to DOC inthroughfall and the Oi layer. However, thecorrelation was weak in Oa leachates. Inaddition, seasonal and annual variation ofDOC/DON ratios indicated different mechanismsand release rates from the forest floor forboth components. The concentrations of DOC andDON in forest floor leachates were in mostcases dependent neither on the pH value orionic strength of the solution, nor on thewater flux or temperature changes. As aconsequence, the DOC and DON fluxes from theforest floor into the mineral soil werelargely dependent on the water flux if annualand biweekly time scales are considered.     

Factors controlling soil water and stream water aluminum concentrations after a clearcut in a forested watershed with calcium-poor soils

The 24 ha Dry Creek watershed in the Catskill Mountains of southeastern New York State USA was clearcut during the winter of 1996–1997. The interactions among acidity, nitrate (NO₃⁻), aluminum (Al), and calcium (Ca²⁺) in streamwater, soil water, and groundwater were evaluated to determine how they affected the speciation, solubility, and concentrations of Al after the harvest. Watershed soils were characterized by low base saturation, high exchangeable Al concentrations, and low exchangeable base cation concentrations prior to the harvest. Mean streamwater NO₃⁻ concentration was about 20 μmol l⁻¹ for the 3 years before the harvest, increased sharply after the harvest, and peaked at 1,309 μmol l⁻¹ about 5 months after the harvest. Nitrate and inorganic monomeric aluminum (Al_im) export increased by 4−fold during the first year after the harvest. Al_im mobilization is of concern because it is toxic to some fish species and can inhibit the uptake of Ca²⁺ by tree roots. Organic complexation appeared to control Al solubility in the O horizon while ion exchange and possibly equilibrium with imogolite appeared to control Al solubility in the B horizon. Al_im and NO₃⁻ concentrations were strongly correlated in B-horizon soil water after the clearcut (r ² = 0.96), especially at NO₃⁻ concentrations greater than 100 μmol l⁻¹. Groundwater entering the stream from perennial springs contained high concentrations of base cations and low concentrations of NO₃⁻ which mixed with acidic, high Al_im soil water and decreased the concentration of Al_im in streamwater after the harvest. Five years after the harvest soil water NO₃⁻ concentrations had dropped below preharvest levels as the demand for nitrogen by regenerating vegetation increased, but groundwater NO₃⁻ concentrations remained elevated because groundwater has a longer residence time. As a result streamwater NO₃⁻ concentrations had not fallen below preharvest levels, even during the growing season, 5 years after the harvest because of the contribution of groundwater to the stream. Streamwater NO₃⁻ and Al_im concentrations increased more than reported in previous forest harvesting studies and the recovery was slower likely because the watershed has experienced several decades of acid deposition that has depleted initially base-poor soils of exchangeable base cations and caused long-term acidification of the soil.     

Composition and deposition of throughfall in a flooded forest archipelago

The sources of spatial and temporal variation and rates of nutrient deposition via throughfall were studied for 9 months in the Anavilhanas archipelago of the Negro River, Brazil. A total of 30 events was sampled individually for rain and throughfall chemistry in a 1-ha plot of flooded forest. Throughfall samples were collected in 40 collectors distributed in five parallel transects in the study plot, while rain was collected in 4 collectors in an adjacent channel. Volume-weighted mean (VWM) concentrations of solutes in rain were consistently lower than in throughfall, except for H⁺, NO ₃ ^– and NH ₄ ⁺ . Ratios of VWM concentrations of rain to throughfall indicated that K⁺, followed by Mg²⁺ and PO ₄ ^3– , were the most enhanced solutes as rain passed through the forest canopy. The deposition of solutes varied significantly among transects, except for Na⁺ and Ca²⁺, and was significantly correlated with maximum flooding depth, foliar nutrient content, soil fertility and canopy closure for most solutes. The concentrations of PO ₄ ^3– and most major ions were higher in throughfall compared to those in rain due to canopy exchange and dry deposition. In contrast, NO ₃ ^– , NH ₄ ⁺ and H⁺ were retained due to immobilization by leafy canopy and ion exchange processes. Solute inputs via throughfall (not including stemflow) to a floodplain lake (Lake Prato) of the archipelago accounted for 30 to 64% of the total for most solutes in the lake at high water, which indicates that throughfall is an important source of nutrients to the aquatic ecosystem of the Anavilhanas archipelago.     

Effect of whole catchment liming on the episodic acidification of two adirondack streams

During the fall of 1989 7.7Mg/ha of calcium carbonate was applied on two tributary catchments (40 ha and 60 ha) to Woods Lake, a small (25 ha) acidic headwater lake in the western Adirondack region of New York. Stream-water chemistry in both catchment tributaries responded immediately. Acid-neutralizing capacity (ANC) increased by more than 200 eq/L in one of the streams and more than 1000 eq/L in the other, from pre-liming values which ranged from –25 to +40 eq/L. The increase in ANC was primarily due to increases in dissolved Ca²⁺ concentrations. Most of the initial response of the streams was due to the dissolution of calcite that fell directly into the stream channels and adjacent wetlands. A small beaver impoundment and associated wetlands were probably responsible for the greater response observed in one of the streams.After the liming of subcatchmentIV (60 ha), Ca²⁺ concentrations increased with increasing stream discharge in the stream during fall rain events, suggesting a contribution from calcite dissolved within the soil and transported to the stream by surface runoff or shallow interflow. Concentrations of other ions not associated with the calcite (e.g. Na⁺) decreased during fall rain events, presumably due to mixing of solute-rich base flow with more dilute shallow interflow. The strong relation between changes in Ca²⁺ and changes in NO ₃ ^– concentrations during spring snowmelt, (r² = 0.93, slope = 0.96, on an equivalent basis) suggests that both solutes had a common source in the organic horizon of the soil. Increases in NO ₃ ^– concentrations during snowmelt were balanced by increases in Ca²⁺ that was released either directly from the calcite or from exchange sites, mitigating episodic acidification of the stream. However, high ambient NO ₃ ^– concentrations and relatively low ambient Ca²⁺ concentrations in the stream during the spring caused the stream to become acidic despite the CaCO₃ treatment.In stream WO2 (40ha), Ca²⁺ concentrations were much higher than in stream WO4 because of the dissolution of calcite which fell directly into the upstream beaver pond and its associated wetlands. Calcium concentrations decreased as both NO ₃ ^– concentrations and stream discharge increased, due to the dilution of Ca-enriched beaver pond water by shallow interflow. Despite this dilution, Ca²⁺ concentrations were high enough to more than balance strong acid anion (SO ₄ ^– , NO ₃ ^– , Cl^–) concentrations, resulting in a positive ANC in this stream throughout the year. These data indicate that liming of wetlands and beaver ponds is more effective than whole catchment liming in neutralizing acidic surface waters.     

Chemical composition of throughfall,soil water,leaves and leaf litter in a beech forest receiving long term application of ammonium sulphate

Nitrogen deposition in the range of 10–40 kg N ha^-1 a^-1 is common in large parts of Europe. Substancial amounts are deposited as NH ₄ ⁺ having fertilization and acidification effects in ecosystems. In a long term experiment the reactions of different compartments of a forest ecosystem were studied when the system became N saturated by continuously applying (NH₄)₂SO₄. The experiment was conducted in a beech forest and the application of 10 kmol_c N ha^-1 a^-1 lasted 11 yr from 1983 till 1993.The results revealed that despite the high soil acidity, the applied NH ₄ ⁺ was quickly oxidized to NO ₃ ^- in the surface 10 cm soil layer and leached to deeper depths. The amount of NO ₃ ^- leached from the surface soil increased during the initial three years and remained constant on a high level for the rest of the experimental period. Nitrification was associated with acidification of the soil solution, causing high concentrations of Al and Mn²⁺ in soil solutions. More than 50% of total Al in solution occurred in non-phytotoxic form (Al–SO₄ complexes). Moreover, concentration of base cations and dissolved organic carbon increased. Concentrations of SO ₄ ^2- in soil solutions increased during the first few years approaching more or less constant values in the surface 40 cm depth, whereas in 40–100 cm depth it took about 10 yr to reach those levels of sulphate concentrations in soils, indicating its retention in the deeper soil layers. No significant change in the chemistry of throughfall water and leaves was observed, indicating to N-saturation of the trees.     

Atmospheric deposition and sulphur cycling in chalk grasslandA mechanistic model simulating field observations

Sulphate fluxes in bulk deposition, throughfall and soil solution were monitored during two years, and integrated within a model describing the cycling of S in a chalk grassland ecosystem. Throughfall fluxes were strongly determined by interceptive properties of the grassland canopy. Seasonal variation in Leaf Area Index resulted in dry deposition velocities for SO₂ varying between 0.1 cm.s^–1 (snow cover, almost no aerodynamic resistance) to 0.9–1.8 cm.s^–1 in periods with a fully developed canopy. On an annual basis net canopy exchange (assimilation of SO₂ minus foliar leaching) was estimated to be –15% of net throughfall. Simulated soil solution concentrations, being the result of throughfall input, leaching, adsorption, biomass uptake and mineralization, closely fitted actual values (r > 0.92; p > 0.001). Actual and simulated leaching were 1.74 ± 0.03 and 2.00 keq.-ha^–1.yr^–1, respectively. Sulphur budgets for the soil showed net accumulation from April to October and net losses from October to April. Annual budgets for the ecosystem showed atmospheric input (2.02keq.ha^–1.yr^–1) and actual output (2.05keq.ha^–1.yr^–1) to be almost balanced. Apart from increased soil solution concentrations, additional input of sulphate (3.55 keq.ha^–1.yr^–1) to experimental plots resulted in additional accumulation in the ecosystem of 0.62 keq.ha^–1.yr^–1