The effects of wildfire on the water chemistry of dilute,acidic lakes in southern Norway

Changes in lake water chemistry were studied for >4 years following a large wildfire in a boreal forest area in Mykland, southern Norway, an area characterized by thin and patchy, base-poor and slow-weathering soils and bedrock. Accordingly, the lakes have low acid neutralizing capacity (ANC), calculated as the difference between the total concentration of base cations ([ΣBC]) and strong acid anions ([SAA]). During the initial post-fire period, and peaking about two months after the fire, the mobilization of SAA from terrestrial to aquatic systems caused a dramatic drop in ANC. In one of the lakes, ANC dropped from about 20 to ?80 μeq L^?1, while [H⁺] and inorganic aluminum ([Al_i]) increased to 38 μeq L^?1 (pH 4.42) and 326 μg Al L^?1 (36.2 μeq L^?1 as Al³⁺), respectively. Sulfate and chloride were the predominant anions responsible for this decline in ANC, as the nitrate increase was small. After the severe chemical episode, [SAA] in the lakes declined faster than [ΣBC], and within about one year after the wildfire, ANC was back to almost pre-fire values. However, despite the fact that [SAA] also continued to decline faster than [ΣBC] the following years, no further increase in ANC was documented. The strong ionic strength decline and the increase in TOC during the same period have likely counteracted for the potential ANC increase. There were large lake-to-lake variations in water chemistry of the wildfire affected lakes. Hydrology, geology, lake residence time and the catchment area to lake area ratio are important explanatory factors.     

Factors controlling long-term changes in soil pools of exchangeable basic cations and stream acid neutralizing capacity in a northern hardwood forest ecosystem

Understanding the factors regulating the concentrations of basic cations in soils and surface waters is critical if rates of recovery are to be predicted in response to decreases in acidic deposition. Using a dynamic simulation model (PnET-BGC), we evaluated the extent to which atmospheric deposition of strong acids and associated leaching by strong anions, atmospheric deposition of basic cations through changes in emissions of particulate matter, and historical forest cutting have influenced soil pools of exchangeable basic cations and the acid-base status of stream water at the Hubbard Brook Experimental Forest (HBEF) in New Hampshire. Historical deposition of basic cations was reconstructed from regression relationships with particulate matter emissions. Simulation results indicate that the combination of these factors has resulted in changes in the percent soil base saturation, and stream pH and acid neutralizing capacity (ANC) from pre-industrial estimates of 20%, 6.3 and 45 eq L^–1, respectively, to current values of 10%, 5.0 and –5 eq L^–1, respectively. These current values fall within the critical thresholds at which forest vegetation and aquatic biotic are at risk from soil and surface water acidification due to acidic deposition. While the deposition of strong acid anions had the largest impact on the acid-base status of soil and stream water, the reduction in deposition of basic cations associated with reductions in particulate emissions was estimated to have contributed about 27% of the depletion in soil Ca²⁺ exchange pool and 15% of the decreases in stream water concentrations of basic cations. Decline in stream water concentrations of basic cation occurred under both increasing and decreasing exchangeable pools, depending on the process controlling the acid base status of the ecosystem. Model calculations suggest that historical forest cutting has resulted in only slight decreases in soil pools of exchangeable basic cations, and has had a limited effect on stream ANC over the long-term.     

Effects of prescribed burning and drought on the solute chemistry of mixed-conifer forest streams of the Sierra Nevada, California

Solute concentrations in atmospheric depositionand stream water were measured in two mixed-conifercatchments (Tharps and Log creeks) in the SierraNevada of California from 1984 through 1995, a periodincluding a 6-year drought and a prescribed burn inone catchment. The effects of prescribed burning inthe Tharps Creek catchment significantly increasedthe concentrations of most solutes in stream water. In the first year after prescribed burning, the VWM(volume-weighted mean) concentrations of acid anionsin stream water increased proportionally more thanthose of the base cations, and ANC (acid neutralizingcapacity) more than doubled. Sulfate and NO ₃ ^- increased proportionally more in streamwater than any other ions after the fire, but pre- andpost-burn VWM pH were not significantlydifferent. VWM SO ₄ ^2- and NO ₃ ^- concentrations the first year after burning occurredwere about 16- and 2,000-fold above pre-burnbaselines, respectively, while that of Cl^-increased 4-fold. Net retention (precipitationinputs minus streamwater outputs) of H⁺,NO ₃ ^- , NH ₃ ⁺ , SO ₄ ^2- and Cl^- occurred in both catchments, except afterprescribed burning of the Tharps Creek catchment inthe fall of 1990, which caused a net export ofSO ₄ ^2- , Cl^- and K⁺ thefirst year after the burn. Most solutes remained abovepre-disturbance concentrations by the end of the thirdyear after burning, whereas H⁺ and SiO₂remained below. Periodic increases in theconcentrations of Na⁺, Ca²⁺ and SO ₄ ^2- , and decreases in ANC and SiO₂occurred during a 6-year drought monitored in theadjacent undisturbed catchment of Log Creek.     

Chemical recovery of acidified Bohemian lakes between 1984 and 2012: the role of acid deposition and bark beetle induced forest disturbance

Assessment of temporal trends and rates of change in hydrochemical parameters and forest cover has been conducted to elucidate key drivers of surface water acidification in glacial lakes in the Czech Republic. Since 1984, the key driver in acidification reversal was sulphate (SO₄) concentration (median decrease of ?3.58 μeq L^?1 yr^?1) which fell in line with reductions in sulphur (S) deposition. Reduction of nitrogen (N) deposition was followed by proportional reduction in nitrate (NO₃) leaching although decline in NO₃ concentrations was more pronounced at two sites, the ?ertovo Lake (CT) and Prá?ilské Lake (PR) until 2006; only ??árské pond showed effective catchment N immobilization. Coherent decline of chloride concentration was detected across all sites. The decrease of strong mineral acids was partly compensated by decrease of inorganic aluminium (Al_in), especially at sites most acidified in the beginning of observations (ANC_1984–1986 between ?160 and ?90 μeq L^?1 at CT, ?erné Lake—CN and Ple?né lake—PL) and by reductions of base cations and increases of pH. All lakes (CN, CT, PL, PR and LK) moved to the ANC range between ?29 and 30 μeq L^?1 (2010–2012) where sensitivity of pH to further reductions in acid anions may be expected. Concurrently, charge of weak organic acids (OAs) increased and partly balanced the strong mineral acid decrease as a consequence of (i) significant DOC (dissolved organic carbon) increase (median change of 0.13 mgC L^?1 yr^?1 since 1993) and (ii) deprotonation of weak OAs caused by pH rise. Since 2000s, bark beetle induced forest decline accelerated NO₃ leaching at most of the catchments (by 200 % at LK, PL and PR). However, elevated N leaching was effectively neutralized by base cations (K, Mg, Ca) originating from decaying fresh litter, thus acidification recovery was not reversed, but slowed down. After cessation of NO₃ leaching we hypothesise that collapsed tree canopy across catchments (from 12 to 87 % compared to 1984) will cause lower total acid input in precipitation (S + N) and regrowth of vegetation may stimulate higher N immobilization (in biomass and soil); processes which could lead to further increase of ANC and pH, key indicators for biological recovery.     

Longitudinal and temporal trends in the water chemistry of the North Branch of the Moose River

Surface water acidification is potentially a problem in regions with low ionic strength drainage waters. Atmospheric deposition of sulfuric acid has generally been implicated as the causative agent of this problem, although other sources of acidity may contribute. The Adirondack region of New York State is an area with acid-sensitive surface waters and an abundance of acidic lakes. The intent of this study was to evaluate the processes regulating the acid/base chemistry of a series of lakes draining a large heterogeneous watershed in the Adirondack region of New York.The study site, the North Branch of the Moose River, is heterogeneous in its soil and geological characteristics. This variability was reflected through differences in water chemistry that occurred within the basin. The northern headwaters generally drain subcatchments with shallow, acidic soils. The resulting water chemistry was acidic (equivalence of acidic anions exceeded equivalence of basic cations) with high concentrations of Al and dissolved organic carbon (DOC). As this water migrated through a large lake (Big Moose Lake) with a moderate hydrologic retention time (0.5 yr), considerable loss of DOC was evident.As acidic water was transported through the drainage area, it mixed with waters that were enriched in concentrations of basic cations from the eastern subbasins. As a result, there was a successive increase in the acid neutralizing capacity (ANC) and a decrease in Al concentrations as water migrated from the northern reaches to the outlet of the watershed.In addition to these general trends, short-term changes in water chemistry were evident. During low flow summer periods concentrations of basic cations were elevated, while concentrations of SO ₄ ^2– and NO ₃ ^– were relatively low. These conditions resulted in less acidic waters (higher ANC) with relatively low concentrations of Al. During high flow winter/spring conditions, elevated concentrations of SO ₄ ^2– and NO ₃ ^– were evident, while concentrations of basic cations were reduced resulting in low pH (low ANC) waters with high concentrations of Al.Variability in the processes regulating the pH buffering of waters was apparent through these short-term changes in water chemistry. In the northern subbasin short-term fluctuations in ANC were minimal because of the buffering of Al under low pH conditions. Seasonal changes in the ANC were more pronounced in the eastern subbasin because of the predominance of inorganic carbon buffering in the circumneutral pH waters.Lakes in the west-central Adirondacks have characteristically short hydraulic residence times and elevated nitric acid inputs. As a result these waters may be more susceptible to surface water acidification than other acid-sensitive lake districts in eastern North America. Given the apparent interregional differences, extrapolation of chemical trends in the Adirondacks to other areas may be tenuous.     

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.     

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.     

Limestone Treatment of Whetstone Brook, Massachusetts. I. Treatment Methodology and Water-Chemistry Changes during Treatment

Whetstone Brook is a trout stream located in north-central Massachusetts that is degraded by acid precipitation. The stream was treated with 56 tonnes of powdered limestone by a prototype, water-powered doser as part of the U.S. Fish and Wildlife Service's Acid Precipitation Mitigation Program. The goal of liming Whetstone Brook was to raise the pH to 6.5 and acid neutralizing capacity (ANC) to at least 50 μeq/1 in a 3.2-km reach. This goal was achieved despite the fact that during the 31 months of treatment stream flow was 37% higher than during the pretreatment period. During the treatment period, pH averaged 6.54 and ANC averaged 69.75. During the pretreatment period average pH was 5.97 and average ANC was 20.26. In the control section of Whetstone Brook, both pH and ANC were lower during the treatment period than during the pretreatment period. During treatment, monomeric aluminum, a form toxic to fish, declined in the treated section and increased in the control section. Total calcium, sediment calcium, and pore-water calcium increased in the treated section during treatment but declined in the control section. The other base anions and cations, nutrients, and physical parameters were not significantly affected by liming.     

Acid-base chemistry and aluminum transport in an acidic watershed and pond in New Hampshire

Cone Pond is one of the few acidic, clear-water ponds in the White Mountains of New Hampshire, a region dominated by high inputs of strong acids from atmospheric deposition and low base content of bedrock. Monitoring was conducted for 13 months to compare and contrast the acid-base chemistry of the terrestrial and aquatic portions of the watershed. Variations in Al concentration and speciation in drainage waters were correlated with changes in the supply of naturally occurring organic ligands. During the study period, the pond retained 28% of Al inputs, including nearly half of the inputs of organically complexed Al. Chemical equilibrium calculations indicated that the entire water-column was oversaturated with respect to the solubility of synthetic gibbsite during summer, as was the hypolimnion during winter. Retention of Al resulted from an increase in pH in the hypolimnion concomitant with SO₄ ^2– reduction, and from loss of organic anions in epilimnetic waters. Acid neutralizing capacity (ANC) generated in the pond primarily through SO₄ ^2– reduction and base cation (C _B ) release was balanced by ANC consumed as a result of Al retention.     

Porewater acid/base chemistry in near-shore regions of an acidic lake

Sediment porewaters in the near-shore region (within 1 m of the shoreline) of an acidic lake (Dart's Lake) were monitored during the summer of 1983 to investigate whether spatial variations in porewater acid/base chemistry were significant in this region of the lake. Previous investigations of Dart's Lake porewaters have indicated that within deeper waters (>2m depth), sediment porewaters are elevated in alkalinity relative to overlying lake water. Within the near-shore region, porewaters both considerably more and less acidic than the lake water were observed. Both reduction of strong acid anions (SO₄ ^2–, NO₃ ^–) and the mobilization of base cations were significant mechanisms of alkalinity production in porewaters exhibiting reducing conditions. In sediments reflecting oxic conditions, porewaters were generally more acidic than the lakewater. Measurement of groundwater seepage into the lake at the near-shore sites indicated that oxic sites exhibited elevated inputs of groundwater when compared to sites where reducing conditions existed. The acidic porewaters associated with high groundwater flows suggests that groundwater inputs to the lake may be a source of acidity (not alkalinity) on a whole-lake basis.     

The biogeochemistry of basic cations in two forest catchments with contrasting lithology in the Czech Republic

The biogeochemistry of Ca, Mg, K, and Nawere investigated in two forested catchments in theCzech Republic, one underlain by leucogranite, theother by serpentinite. High weathering rates at theserpentinite site at Pluhv Bor resultedin Mg²⁺ as the dominant cation on the soilexchange complex and in drainage water. Other basiccations (Ca²⁺, K⁺, Na⁺) showedrelatively low concentrations and outflow instreamwater. The catchment exhibited high basesaturation in mineral soils (>70%), and nearneutral soil and stream pH, despite elevated inputsof acidic deposition. Slow growth of Norway spruceat Pluhv Bor may be caused by K deficiency, Mgoversupply and/or Ni toxicity. In contrast, thegranitic site at Lysina showed low concentrations ofbasic cations on the soil exchange complex and instreamwater. Soil and drainage water at Lysina werehighly impacted by acidic deposition. Soil pH wasextremely acidic (<4.5) throughout the soilprofile, and the base saturation of the mineral soilwas very low (<5%). Supplies of basic cationsfrom atmospheric deposition and soil processes wereless than inputs of SO^2- ₄ on anequivalence basis, resulting in low pH and highconcentrations of total Al in drainage water. Needle yellowing in Norway spruce was possibly theresult of Mg deficiency at Lysina. Because of theirextremely different lithologies, these catchmentsserve as valuable end-members of ecosystemsensitivity to elevated levels of acidicdeposition.     

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.     

Forest regrowth as the controlling factor of soil nutrient availability 75 years after fire in a deciduous forest of Southern Quebec

The effects of secondary succession on soil nutrient availability following fire in the 1920s was investigated in a hardwood forest of southern Quebec by correlation analyses between soil and solution chemistry, tree species composition, tree growth, litterfall nutrient fluxes and presence of charcoal monitored in six 300 m² plots between 1994 and 1998. The results suggests that the pioneer stand of largetooth aspen, paper birch and yellow birch that followed fire enriched the forest floor and upper mineral soil with its K-rich litter, but lowered solution NH₄, NO₃ and Mg concentrations through its high nutrient demand. High woody biomass primarily observed in the maple-dominated stands was associated with low exchangeable base cation concentrations in the forest floor, suggesting that nutrient immobilisation in trees is also a significant process leading to spatial variation in base cation availability in the forest floor. Finally, charcoal was positively correlated with exchangeable base cations in the forest floor which leads to believe that charcoal has a high affinity for base cations and that it can increase base cation availability decades after forest fire disturbance.     

DIATOM COMMUNITY DYNAMICS IN STREAMS OF CHRONIC AND EPISODIC ACIDIFICATION: THE ROLES OF ENVIRONMENT AND TIME1

Community dynamics of epiphytic diatoms were studied for 3 years in a chronically and an episodically acidified tributary of Buck Creek, Adirondacks. Both streams experienced pulses of acidity during hydrologic events but these pulses were more pronounced in the episodically acidified stream, where pH decreased over two units (between 4.53 and 6.62) and the acid‐neutralizing capacity (ANC) became negative. In the chronically acidified stream, pH was below 4.9 and the ANC was negative 94% of the time. In this stream, high inorganic acidity following SO₄^2? enrichment from snowmelt or rainstorms alternated with high organic acidity derived from a headwaters wetland during base flow. The fluctuating water chemistry generated shifts in diatom community composition: from exclusive dominance of Eunotia bilunaris (Ehrenberg) Mills during periods of high inorganic acidity to proliferation of several subdominant species during periods of high organic acidity. In the episodically acidified stream, the pulses of acidity were associated with high NO₃^? concentrations and the corresponding high ratios of inorganic monomeric Al (Al_im) to organic monomeric Al (Al_om). Diatom communities there were dominated exclusively by E. exigua (Brébisson) Rabenhorst year round; however, this species peaked during periods of low acidity. Periods of high acidity and Al_im:Al_om ratios were marked by a decline in E. exigua and a concomitant increase in the subdominant species. Variance partitioning into terms of environmental and temporal variance, and their covariance, suggested that diatom communities in the chronically acidic stream were governed primarily by environmental factors while in the episodically acidic stream environmental and temporal factors had equal contributions.     

Processes controlling DOC in pore water during simulated drought cycles in six different UK peats

The effect of episodic drought on dissolved organic carbon (DOC) dynamics in peatlands has been the subject of considerable debate, as decomposition and DOC production is thought to increase under aerobic conditions, yet decreased DOC concentrations have been observed during drought periods. Decreased DOC solubility due to drought-induced acidification driven by sulphur (S) redox reactions has been proposed as a causal mechanism; however evidence is based on a limited number of studies carried out at a few sites. To test this hypothesis on a range of different peats, we carried out controlled drought simulation experiments on peat cores collected from six sites across Great Britain. Our data show a concurrent increase in sulphate (SO₄) and a decrease in DOC across all sites during simulated water table draw-down, although the magnitude of the relationship between SO₄ and DOC differed between sites. Instead, we found a consistent relationship across all sites between DOC decrease and acidification measured by the pore water acid neutralising capacity (ANC). ANC provided a more consistent measure of drought-induced acidification than SO₄ alone because it accounts for differences in base cation and acid anions concentrations between sites. Rewetting resulted in rapid DOC increases without a concurrent increase in soil respiration, suggesting DOC changes were primarily controlled by soil acidity not soil biota. These results highlight the need for an integrated analysis of hydrologically driven chemical and biological processes in peatlands to improve our understanding and ability to predict the interaction between atmospheric pollution and changing climatic conditions from plot to regional and global scales.     

Chemical composition of forest floor and consequences for nutrient availability after wildfire and harvesting in the boreal forest

In boreal forests of eastern Canada, wildfire has gradually been replaced by clearcut harvesting as the most extensive form of disturbance. Such a shift in disturbance may influence the chemical properties of the forest floor and its capacity to cycle and supply nutrients, with possible implications for forest productivity. We compared the effects of stem-only harvesting (SOH), whole-tree harvesting (WTH) and wildfire on the chemical composition of forest floor organic matter and nutrient availability for plants, 15–20 years after disturbance in boreal coniferous stands in Quebec (Canada). The forest floor on plots of wildfire origin was significantly enriched in aromatic forms of C with low solubility, whereas the forest floor from SOH and WTH plots was enriched with more soluble and labile C compounds. The forest floor of wildfire plots was also characterized by higher N concentration, but its high C:N and high concentration of ¹⁵N suggest that its N content could be recalcitrant and have a slow turnover rate. Total and exchangeable K were associated with easily degradable organic structures, whereas total and exchangeable Ca and Mg were positively correlated with the more recalcitrant forms of C. We suggest that the bulk of Ca and Mg cycling in the soil–plant system is inherited from the influx of exchangeable cations in the forest floor following disturbance. The buildup of Ca and Mg exchangeable reserves should be greater with wildfire than with harvesting, due to the sudden pulse of cation-rich ash and to the deposition of charred materials with high exchange capacity. This raises uncertainties about the long-term availability of Ca and Mg for plant uptake on harvested sites. In contrast, K availability should not be compromised by either harvesting or wildfire since it could be recycled rapidly through vegetation, litter and labile organic compounds.     

Wildfire potential evaluation during a drought event with a regional climate model and NDVI

Regional climate modeling is a technique for simulating high-resolution physical processes in the atmosphere, soil and vegetation. It can be used to evaluate wildfire potential by either providing meteorological conditions for computation of fire indices or predicting soil moisture as a direct measure of fire potential. This study examines these roles using a regional climate model (RCM) for the drought and wildfire events in 1988 in the northern United States. The National Center for Atmospheric Research regional climate model (RegCM) was used to conduct simulations of a summer month in each year from 1988 to 1995. The simulated precipitation and maximum surface air temperature were used to calculate the Keetch–Byram Drought Index (KBDI), which is a popular fire potential index. We found that the KBDI increased significantly under the simulated drought condition. The corresponding fire potential was upgraded from moderate for a normal year to high level for the drought year. High fire potential is often an indicator for occurrence of intense and extensive wildfires. Fire potential changed in the opposite direction for the 1993 flood event, indicating little possibility of severe wildfires. The soil moisture and KBDI evaluations under the drought and flood conditions are in agreement with satellite remotely sensed vegetation conditions and the actual wildfire activity. The precipitation anomaly was a more important contributor to the KBDI changes than temperature anomaly. The small magnitude of the simulated soil moisture anomalies during the drought event did not provide sufficient evidence for the role of simulated soil moisture as a direct measure of wildfire potential.     

Long-term trends in soil solution and stream water chemistry at the Hubbard Brook Experimental Forest: relationship with landscape position

In acid-sensitive watersheds of the northeastern US, decreases in SO₂ emissions and atmospheric deposition of sulfur have not been accompanied by marked changes in pH and acid neutralizing capacity (ANC). To better understand this phenomenon, we investigated the long-term trends in soil solution (1984–1998) and stream water (1982–2000) chemistry along a natural soil catena at the Hubbard Brook Experimental Forest, New Hampshire, USA. Significant declines in strong acid anion concentrations were accompanied by declines in base cation concentrations in soil solutions draining the Oa and Bs soil horizons at all elevations. The magnitude of change varied with position in the landscape. Recovery, as indicated by increasing ANC (mean 2.38µEqL^–1year^–1) and decreasing concentrations of inorganic monomeric Al (mean 1.03µmolL^–1year^–1), was confined to solutions draining the Bs horizon at mid-to-higher elevations. However, persistently low Ca²⁺/Al_i ratios (<1) in Bs soil solutions at these sites may be evidence of continuing Al stress to trees. In Bs soil solution at a lower elevation site and in Oa soil solutions at all sites, declines in base cations (mean 3.71µEqL^–1year^–1) were either similar to or exceeded declines in strong acid anions (mean 3.25µEqL^–1year^–1) resulting in no change in ANC. Changes in the chemistry of stream water reflected changes in soil solutions, with the greatest improvement in ANC occurring at high elevation and the rate of increase decreasing with decreases in elevation. The pH of soil solutions and stream waters either declined or did not change significantly. Therefore pH-buffering processes, including hydrolysis of Al and possibly the deprotonation of organic acids, have prevented increases in drainage water pH despite considerable reductions in inputs of strong acids.     

Soil nitrogen dynamics three years after a severe Araucaria–Nothofagus forest fire

Wildfires have shaped the biogeography of south Chilean Araucaria–Nothofagus rainforest vegetation patterns, but their impact on soil properties and associated nutrient cycling remains unclear. Nitrogen (N) availability shows a site‐specific response to wildfire events indicating the need for an increased understanding of underlying mechanisms that drive changes in soil N cycling. In this study, we selected unburned and burned sites in a large area of the National Park Tolhuaca that was affected by a stand‐replacing wildfire in February 2002. We conducted net N cycling flux measurements (net ammonification, net nitrification and net N mineralization assays) on soils sampled 3 years after fire. In addition, samples were physically fractionated and natural abundance of C and N, and ¹³C‐NMR analyses were performed. Results indicated that standing inorganic N pools were greater in the burned soil, but that no main differences in net N cycling fluxes were observed between unburned and burned sites. In both sites, net ammonification and net nitrification fluxes were low or negative, indicating N immobilization. Multiple linear regression analyses indicated that soil N cycling could largely be explained by two parameters: light fraction (LF) soil organic matter N content and aromatic Chemical Oxidation Resistant Carbon (COREC_arom), a relative measure for char. The LF fraction, a strong NH₄⁺ sink, decreased as a result of fire, while COREC_arom increased in the burned soil profile and stimulated NO₃^‐ production. The absence of increased total net nitrification might relate to a decrease in heterotrophic nitrification after wildfire. We conclude that (i) wildfire induced a shift in N transformation pathways, but not in total net N mineralization, and (ii) stable isotope measurements are a useful tool to assess post‐fire soil organic matter dynamics.     

Impact of faunal complexity on nutrient supply in field mesocosms from a spruce forest soil

A field study in an acidic spruce forest soil using soil mesocosms was conducted to investigate the effects of mesofauna and macrofauna on exchangeable cations, organic matter content, base saturation, and Ca-lactate extractable nutrients. In the field, intact soil monoliths were taken from the ground, defaunated by deep-freezing and wrapped in nets of various mesh-sizes to control immigration of different faunal size classes. The monoliths were then replanted in the field. Three types of treatments for the mesocosms were prepared: (1) microbiota only, (2) microbiota and mesofauna, (3) microbiota, mesofauna, and macrofauna (=complex fauna). After eight months the mesocosms and unmanipulated control plots (treatment 4) were destructively sampled and submitted to chemical analysis. Generally, the exchangeable base cations and Mn²⁺ showed higher contents with increasing faunal complexity, whereas the exchangeable acidic cations of Fe³⁺ and Al³⁺ decreased in the monoliths with complex fauna. These effects were significant for K⁺, Mg²⁺ and Mn²⁺ in the L/F-layer and for Ca²⁺, Mn²⁺, Al³⁺ and Fe³⁺ in the H-layer. As a possible explanation a rise of ion-binding sites in the course of enhanced humification processes is discussed.In the L/F-layer base cations showed higher concentrations in the monoliths with complex fauna as compared to the control plot, which contained intact roots. This might be due to nutrient uptake by roots in the control plot or enhanced mineralization in the monoliths with complex fauna, where roots had been cut.