Phosphorus mineralization in subarctic agricultural and forest soils

Summary Potential P and C mineralization rates were determined in a 12-week laboratory incubation study on subarctic forest and agricultural soil samples with and without N fertilizer added. There was no significant difference in net inorganic P produced between N fertilized and unfertilized soils. The forest soil surface horizons had the highest net inorganic P mineralized, 32 mg P kg^-1 soil for the Oie and 17 mg P kg^-1 soil for the Oa. In the cropped soils net inorganic P immobilization started after 4 weeks and lasted through 12 weeks of incubation. Cumulative CO₂–C evolution rates differed significantly among soils, and between fertilizer treatments, with the N-fertilized soils evolving lower rates of CO₂–C than the unfertilized soils. Soils from the surface horizons in the forest evolved the highest rates of CO₂–C (127.6 and 89.4 mg g^-1 soil for the Oie and Oa horizons, respectively) followed by the cleared uncropped soil (42.8 mg g^-1 soil C), and the cropped soils (25.4 and 29.0 mg g^-1 soil C). In vitro soil respiration rates, or potential soil organic matter decomposition rates, decreased with increasing time after clearing and in accord with the degree of disturbance. Only soils with high potential C mineralization rates and high organic P to total P ratios, mineralized P by the end of the study. Mineralizable P appeared to be associated with readily mineralizable organic C.     

Denitrification potential of intermittently saturated floodplain soils from a subtropical perennial stream and an ephemeral tributary

Denitrification has the potential to remove excess nitrogen from groundwater passing through riparian buffers, thus improving water quality downstream. In regions with markedly seasonal precipitation, transient stream flow events may be important in saturating adjacent floodplain soils and intermittently providing the anaerobic conditions necessary for denitrification to occur. In two experiments we characterised the denitrification potential of soils from two contrasting floodplains that experience intermittent saturation. We quantified under controlled laboratory conditions: 1) potential rates of denitrification in these soils with depth and over time, for a typical period of saturation; and 2) the influences on rates of nitrate and organic carbon. Treatments differed between experiments, but in each case soil-water slurries were incubated anaerobically with differing amendments of organic carbon and nitrate; denitrification rates were measured at selected time intervals by the acetylene-block technique; and slurry filtrates were analysed for various chemical constituents. In the first experiment (ephemeral tributary), denitrification was evident in soils from both depths (0-0.3 m; 0.3-1.1 m) within hours of saturation. Before Day 2, mean denitrification rates at each depth were generally comparable, irrespective of added substrates; mean rates (Days 0 and 1) were 5.2 ± 0.3 mg N kg dry soil⁻¹ day⁻¹ (0-0.3 m) and 1.6 ± 0.2 mg N kg dry soil⁻¹ day⁻¹ (0.3-1.1 m). Rates generally peaked on Days 2 or 3. The availability of labile organic carbon was a major constraint on denitrification in these soils. Acetate addition greatly increased rates, reaching a maximum in ephemeral floodplain soils of 17.4 ± 1.8 mg N kg dry soil⁻¹ day⁻¹ on Day 2: in one deep-soil treatment (low nitrate) this overcame differences in rates observed with depth when acetate was not added, although the rate increase in the other deep-soil treatment (high nitrate) was significantly less (P ≤ 0.01). Without acetate, peak denitrification rates in this experiment were 6.9 ± 0.4 and 2.8 ± 0.2 mg N kg dry soil⁻¹ day⁻¹ in surface and deep soils, respectively. Differences in rates were observed with depth on all occasions, despite similar initial concentrations of dissolved organic carbon (DOC) at both depths. Levels of substrate addition in the second experiment (perennial stream) more closely reflected natural conditions at the site. Mean denitrification rates were consistently much higher in surface soil (P ≤ 0.001), while the source of water used in the slurries (surface water or groundwater from the site) had little effect on rates at any depth. Mean rates when all treatments retained nitrate were: 4.5 ± 0.3 mg N kg dry soil⁻¹ day⁻¹ (0-0.3 m depth); 0.8 ± 0.3 mg N kg dry soil⁻¹ day⁻¹ (0.3-1.0 m); and 0.6 ± 0.1 mg N kg dry soil⁻¹ day⁻¹ (1.8-3.5 m). For comparable treatments and soil depths, denitrification potentials at both sites were similar, apart from higher initial rates in the ephemeral floodplain soils, probably associated with their higher DOC content and possibly also their history of more frequent saturation. The rapid onset of denitrification and the rates measured in these soils suggest there may be considerable potential for nitrate removal from groundwater in these floodplain environments during relatively short periods of saturation.     

Changes in aggregate stability,nutrient status,indigenous microbial populations,and seedling emergence,following inoculation of soil withNostoc muscorum

The potential of the N₂-fixing cyanophyteNostoc muscorum for improving the aggregate stability of a poorly structured silt loam soil was studied in a greenhouse experiment. Inoculum rates were 1.61×10⁵ cells g^-1 soil dry weight (low rate) and 4.04×10⁵ cell g^-1 soil dry weight (high rate), approximately equivalent to a field application of 2 and 5 kg ha^-1 cells dry weight, respectively.N. muscorum numbers had increased 8-fold (low rate) and 10-fold (high rate) by 300 days after inoculation, indicating not only survival but proliferation. Increases in soil polysaccharides, determined as soil carbohydrate C, were 2.96–3.49 time the values in the non-inoculated soils and aggregate stability had incrased by an average of 18% on day 300. Inoculation withN. muscorum also had a pronounced effect on soil chemical and biological properties, with total C increasing by 50–63% and total N increasing by 111–120%. Increases in the soil indigenous microbial population were recorded, with numbers of bacteria 500, fungi 16, and actinomycetes 48 times the non-inoculated values on day 300 in the high-rate soil. The emergence of lettuce seedlings (Lactuca sativa var. Saladin) in undisturbed inoculated 300-day soils was 56% (low rate) and 52% (high rate) higher than in non-inoculated soils. However, homogenising soils and irrigating (to smulate ploughing and surface crusting) significantly reduced this increase in both treatments, although emergence in inoculated soils was still greater by 45% (low) and 24% (high). It is recommended that inoculated soils be left undisturbed prior to planting. The effects ofN. muscorum on soil physical, chemical, and biological properties indicate the possible benefits of cyanobacteria as soil inoculants, not only for the improvement of soil aggregate stability but also as a means of improving seedling emergence.     

Transformations of mineral nitrogen applied to peat soil during sequential oxic/anoxic cycling

Shifts in oxic and anoxic conditions in soil are most frequently caused by water table fluctuations, heavy rain, snowmelt or flooding, with potentially significant impacts on microbial processes and the ability of soils to convert mineral nitrogen to nitrogen gases efficiently. The impact of oxic/anoxic cycles on nitrogen transformation rates was therefore explored in the upper layer (0-30 cm) of partially degraded peat soil. We hypothesized that high denitrification potential would be conserved due to the high organic matter content of this soil. Mineral nitrogen was applied to approximately 1-cm deep layers of homogenized soil in microcosms, with no external source of readily degradable carbon. Microcosms were subjected to three cycles, each consisting of an oxic phase of 8-11 days and an anoxic phase of 21-28 days. Approximately 2% of the ammonium load was lost through ammonia volatilization during oxic phases and the remainder was nitrified. The accumulated nitrate decreased soil pH from 8.0 to 6.8 before its transformation through denitrification. Nitrification and denitrification rates during the three oxic/anoxic cycles (approximately three months) were 2.9-3.2 kg N ha⁻¹ d⁻¹ and 1.0-2.3 kg N ha⁻¹ d⁻¹, respectively. Extrapolation of these values to 30-cm deep soil layers gave rates that were sufficient for complete transformation of at least 1700 kg N ha⁻¹ of ammonium to nitrogen gases, which is ten-fold greater than the annual nitrogen application of 170 kg N ha⁻¹ permitted by the European directive. Denitrification rates decreased linearly during the three cycles (from 36 ± 2 to 16 ± 1 μg N g⁻¹ d⁻¹ dry soil), projecting cessation of denitrification activity and CO₂ production during the fifth cycle. Storage of peat soil at 4 °C most probably allowed slow degradation of organic matter that was completely oxidized to CO₂ after the soil was exposed to higher temperature (28 °C). Storage of soil for one year did not affect nitrification rate, but reduced denitrification rate, unless soil was amended with a readily degradable carbon source. The data suggest that, despite the high carbon content of this soil, it cannot sustain transformations of high N loads to nitrogen gases for prolonged periods without amendment with readily available carbon.     

Estimation of sulfur mineralization and relationships with nitrogen and carbon in soils

A 25-week laboratory study was carried out to determine sulfur, carbon, and nitrogen mineralization rates in soil samples obtained from representative soils in France. Their relationship with some of the soil properties was investigated to find a predictor of mineralized S in soils. At 20°C and 80% water-holding capacity, the S mineralization rate ranged from 0.02 to 0.16 mg kg⁻¹ day⁻¹. It was significantly positively related to soil organic C and N and to C and N mineralization rates. It was weakly related to total soil S. The results suggest that the S mineralization is predominantly driven by heterotrophic microbial activity. A predictive equation for S mineralization based on soil C content, soil pH, and clay content is proposed.     

Mineralization and denitrification in upland, nearly saturated and flooded subtropical soil I. Effect of nitrate and ammoniacal nitrogen

 The influence of fertilizer N applied through nitrate and ammoniacal sources on the availability of nitrate, supply of C, and gaseous N losses via denitrification (using acetylene inhibition technique) in a semiarid subtropical soil (Typic Ustochrepts) was investigated in a growth chamber simulating upland [60% water-filled pore space (WFPS)], nearly saturated (90% WFPS), and flooded (120% WFPS) conditions. The rate of denitrification was very low in the upland soil conditions, irrespective of fertilizer N treatments. Increasing water content to nearly saturated and flooded conditions resulted in four- to sixfold higher rates of denitrification within 2 days, suggesting that the denitrifying activity commences quickly. Results of this study reveal that (1) under restricted aeration, these soils could support high rates of denitrification (∼6 mg N kg^–1 day^–1) for short periods when nitrate is present; (2) application of fertilizer N as nitrate enhances N losses via denitrification (∼10 mg N kg^–1 day^–1) – however, the supply of available C determines the intensity and duration of denitrification; (3) when fertilizer N is applied as an ammoniacal form, nitrification proceeds slowly and nitrate availability limits denitrification in flooded soil; (4) the nearly saturated soil, being partially aerobic, supported greater nitrification of applied ammoniacal fertilizer N than flooded soil resulting in higher relative rates of denitrification; and (5) under aerobic soil conditions, 26 mg mineral N kg^–1 accumulated in control soil over a 16-day period, demonstrating a modest capacity of such semiarid subtropical soils, low in organic matter, to supply N to growing plants. Received: 7 June 1999     

Influence of texture on habitable pore space and bacterial-protozoan populations in soil

Summary Soil texture affects pore space, and bacterial and protozoan populations in soil. In the present study we tested the hypothesis that bacteria are more protected from protozoan predation in fine-textured soils than in coarse-textured soils because they have a larger volume of protected pore space available to them. The experiment consisted of three sterilized Orthic Black Chernozemic soils (silty clay, clay loam, and sandy loam) inoculated with bacteria, two treatments (with and without protozoa), and five sampling dates. The soils were amended with glucose and mineral N on day 0. On day 4 bacterial numbers in all three soils were approximately 3×10⁹ g^–1 soil. The greatest reduction in bacteria due to protozoan grazing occurred between day 4 and day 7. Compared to the treatment without protozoa, bacteria in the treatment with protozoa were reduced by 68, 50, and 75% in the silty clay, clay loam, and sandy loam, respectively. On day 4, 2 days after the protozoan inoculation, all protozoa were active. The numbers were 10330, 4760, and 15 380 g^–1 soil for the silty clay, clay loam, and sandy loam, respectively. Between day 4 and day 7, the period of greatest bacterial decline, total protozoa increased greatly to 150480, 96160, and 192100 g^–1 soil for the three soils, respectively. Most protozoa encysted by day 7. In all soils the addition of protozoa significantly increased CO₂–C evolution per g soil relative to the treatment without protozoa. Our results support the hypothesis that bacteria are more protected from protozoan predation in fine-textured soils than in coarse-textured soils.     

Effect of extracellular-enzyme activities on solubilization rate of soil organic nitrogen

In a sandy soil containing ¹⁵N-labeled active (soluble and easily degradable) and non-labelled passive (recalcitrant) fractions of soil organic matter, the rate of net N mineralization (solubilization) was determined during a 55-day incubation at 25°C, 63% water-holding capacity and different levels of soil extracellular-enzyme activities. The active fraction of soil N was labelled by preincubation (at 5°C and 74% water-holding capacity for 6 months) of soil amended with ¹⁵N-labeled plant material. Increases in the activity of extracellular-enzymes in soil were induced by the addition of glucose and KH₂PO₄ at the beginning of the incubation. The results show that the contents of total soluble N (NO ₃ ^– –N+NH ₄ ⁺ –N + soluble organic N) were significantly higher in glucose-amended soil compared to the unamended soil. The increases in soluble N in soil amended with 1 and 2 mg glucose g^-1 dry soil corresponded to a mean rate of net solubilization of 7.9±1.4 and 18.8±0.7 nmol N g^-1 dry soil day^-1, respectively. The mean rate of net N solubilization (3.6±1.0 nmol N g^-1 dry soil day^-1) in unamended soil was significantly lower than those of glucose amended soils. The content of ¹⁵N in total soluble N in soil amended with 2 mg glucose, for example, was diluted from 3.11±0.08 atom% before the incubation to 2.77±0.03 atom% after 55 days. This indicates that 89% of soluble-N accumulated in soil by the end of the incubation originated from the active fraction of soil N and the rest, estimated at 11%, originated from the passive fraction. The activities of soluble and total proteases as well as the rate of N solubilization in the soil increased with the application of glucose. The activity of these extracellular enzymes was highly correlated with the rates of net N solubilization. Thus, increases in extracellular-enzyme activities in glucose-amended soils had a priming effect on the solubilization of ¹⁵N-labeled active and non-labeled passive fractions of soil organic N. It seems that the activity of extracellular-enzymes expressed in terms of total and soluble protease activities could be a rate-limiting factor in the processes of soil organic N solubilization.     

What predicts nitrous oxide emissions and denitrification N-loss from European soils?

N₂0 emissions and denitrification N-losses. precipitation, air temperature, soil moisture, bulk density and content of mineral N were monitored in 9 different agricultural soils in 6 European countries throughout the vegetation period (April to September) 1992 and 1993. N₂O emissions and denitrification N-losses were log-normal distributed, reflecting high temporal changes. While small flux rates (< 2 g N ha^?1 d^?1) were detectable every day, high rates (> 10 g N ha^?1 d^?1) were measured after fertilization. An attempt to relate the emission variables to climate and soil variables was made through the use of correlation analysis. The mean N₂0 emissions from soil were significantly correlated with the soil properties clay, organic C and mineral N content and the amount of applied mineral N fertilizer. The best prediction of the N₂O emission rates (r² = 0.734) was achieved by multiple linear regression using the soil parameter clay and mineral N. Only 50% of the observed variation could be explained by the factors C_org and mineral N, which describe the substrate availability for microbial processes. No successful statistical model was found for the prediction of denitrification N-losses.     

Nitrogen mineralization, nitrification and denitrification potential in contrasting lowland rain forest types in Central Kalimantan, Indonesia

Nitrogen mineralization and denitrification potential in litter were measured during a dry and a wet period in a Bornean Lowland Evergreen Rain Forest (LERF) and two nearby Heath Forests (HF) of contrasting stature. Nitrification was very low or non-existent in all forest types and ammonification was the major constituent of nitrogen (N) mineralization. Rates of net N mineralization in the HFs on infertile sandy soils were lower than in the LERF on a more nutrient-rich clay soil or other LERFs, both during dry and wet conditions. We attribute the differences to the lower litter quality in the HFs compared to LERF. When dissolved organic nitrogen (DON-N) was included, N uptake was the same (15-17 μg g⁻¹ d⁻¹) in all three forest types. We conclude that N availability is the same in all three forest types and that N deficiency is not the reason for the reduced stature of Heath Forests compared to LERF. All three-forest types had denitrifiers present in the ectorganic layers but denitrification will only play a minor role in the N-cycle as nitrification rates were very low.     

Denitrification activity in the root zone of a sludge-amended desert soil

Summary We evaluated potential NO _inf3 ^sup- losses from organic and inorganic N sources applied to improve the growth of cotton (Gossypium hirsutum) on a Pima clay loam soil (Typic Torrifluvent). An initial set of soil cores (April 1989) was collected to a depth of 270 cm from sites in a cotton field previously amended with anaerobically digested sewage sludge or an inorganic N fertilizer. The denitrification potential was estimated in all soil samples by measuring N₂O with gas chromatography. Soils amended with a low or high rate of sludge showed increased denitrification activity over soil samples amended with a low rate or inorganic N fertilizer. All amended samples showed greater denitrification activity than control soils. The denitrification decreased with soil depth in all treatments, and was only evident as deep as 90 cm in the soils treated with the high sludge rate. However, when soils collected from depths greater than 90 cm were amended with a C substrate, significant denitrification activity occurred. These date imply that organisms capable of denitrification were present in all soil samples, even those at depths far beneath the root zone. Hence, denitrification was C-substrate limited. A second series of soil cores taken later in the growing season (July 1989) confirmed these data. Denitrification losses (under laboratory conditions) to a soil depth of 270 cm represented 1–4% of total soil N depending on treatment, when the activity was C-substrate limited. With additional C substrate, the denitrification losses increased to 15–22% of the total soil N.     

Denitrification loss from a grassland soil in the field receiving different rates of nitrogen as ammonium nitrate

Denitrification loss from a loam under a cut ryegrass sward receiving 0, 250 and 500 kg N ha^?1 a^?1 in four equal amounts was measured during 14 months using the acetylene-inhibition technique. The rate of denitrification responded rapidly to changes in soil water content as affected by rain. Mean rates of denitrification exceeded 0.2 kg N ha^?1 day^?1 only when the soil water content was >20% (w/w) and nitrate was >5μ N g^?1 in the upper 20 cm of the profile and when soil temperature at 2 cm was >5–8°C. When the soil dried to a water content <20%, denitrification decreased to <0.05 kg N ha^?1 day^?1. Highest rates (up to 2.0 kg N ha^?1 day^?1) were observed following application of fertilizer to soil at a water content of about 30% (w/w) in early spring. Denitrification in the control plot during this period was generally about a hundredth of that in plots treated with ammonium nitrate. High rates of N₂O loss (up to 0.30 kg N ha^?1 day-1) were invariably associated with high rates of denitrification (> 0.2 kg N ha^?1 day^?1). However, within 2–3 weeks following application of fertilizer to the plot receiving 250 kg N ha^?1 a^?1 the soil acted as a sink for atmospheric N₂O when its water content was >20% and its temperature >5–8°C. Annual N losses arising from denitrification were 1.6, 11.1 and 29.1 kg N ha^?1 for the plots receiving 0, 250 and 500 kg N ha^?1 a^?1, respectively. More than 60% of the annual loss occurred during a period of 8 weeks when fertilizer was applied to soil with a water content >20%.     

Differences in the activity and bacterial community structure of drained grassland and forest peat soils

The microbial activity and bacterial community structure were investigated in two types of peat soil in a temperate marsh. The first, a drained grassland fen soil, has a neutral pH with partially degraded peat in the upper oxic soil horizons (16% soil organic carbon). The second, a bog soil, was sampled in a swampy forest and has a very high soil organic carbon content (45%), a low pH (4.5), and has occasional anoxic conditions in the upper soil horizons due to the high water table level. The microbial activity in the two soils was measured as the basal and substrate-induced respiration (SIR). Unexpectedly, the SIR (μl CO₂ g⁻¹ dry soil) was higher in the bog than in the fen soil, but lower when CO₂ production was expressed per volume of soil. This may be explained by the notable difference in the bulk densities of the two soils. The bacterial communities were assessed by terminal restriction fragment length polymorphism (T-RFLP) profiling of 16S rRNA genes and indicated differences between the two soils. The differences were determined by the soil characteristics rather than the season in which the soil was sampled. The 16S rRNA gene libraries, constructed from the two soils, revealed high proportions of sequences assigned to the Acidobacteria phylum. Each library contained a distinct set of phylogenetic subgroups of this important group of bacteria.     

Mineral-fixed ammonium in clay- and silt-size fractions of soils incubated with 15N-ammonium sulphate for five years

Summary Four soils with 6, 12, 23, and 47% of clay were incubated for 5 years with ¹⁵N-labeled (NH_{4 2}SO₄ and hemicellulose. The incubations took place at 20°C and 55% water-holding capacity. Samples of whole soils, and clay- (<2 m) and silt-(2–20 m) size fractions (isolated by ultrasonic dispersion and gravity sedimentation) were analysed for labeled and native mineral-fixed ammonium. Mineral-fixed ammonium in non-incubated soil samples accounted for 3.4%–8.3% of the total N and showed a close positive correlation with the soil clay content (r ² = 0.997). After 5 years of incubation, the content of mineral-fixed ammonium in the clay fraction was 255–430 g N g^–1, corresponding to 71%–82% of the mineral-fixed ammonium in whole soils. Values for silt were 72–166 g N g^–1 (14%–33% of whole soil content). In the soils with 6% and 12% clay, less than 1 % of the labeled clay N was present as mineral-fixed ammonium. In the soil with 23% clay, 3% of the labeled N in the clay was mineral-fixed ammonium. Labeled mineral-fixed ammonium was not detected in the silt fractions. For whole soils, and clay and silt fractions, the proportion of native N present as mineral-fixed ammonium varied between 3% and 6%. In contrast, the proportion of labeled N found as mineral-fixed ammonium in the soil with 4701o clay was 23%, 38% and 31% for clay, silt, and whole-soil samples, respectively. Corresponding values for native mineral-fixed ammonium were 12%, 16%, and 10%. Consequently, studies based on soil particle-size fractions and addressing the N turnover in clay-rich soils should consider the pool of mineral-fixed ammonium, especially when comparing results from different size fractions with those from fractions isolated from soils of a widely different textural composition.     

Saturated hydraulic conductivity of soils in the Southern Piedmont of Georgia,USA: Field evaluation and relation to horizon and landscape properties

Saturated hydraulic conductivity (K_s) is one of the soil properties used most often to predict soil behavior and suitability for a variety of uses. Because of the difficulty in K_s measurement and its variability with depth and across the landscape, K_s is commonly predicted from other more easily evaluated properties including texture, clay mineralogy, bulk density, pedogenic structure and cementation. Of these, texture and pedogenic structure are most commonly used to estimate K_s, but the reliability of these estimates has not been evaluated for common soils in the Southern Piedmont of Georgia. Thus, the objectives of this study were to evaluate K_s for major horizons in soils and landscapes in the Georgia Piedmont and to relate K_s to morphological properties of these horizons. Ten sites across the region were selected, and 21 pedons arranged in three transects were described from auger holes and pits. For each pedon, K_s was measured in upper Bt horizons, at 140 cm below the surface (Bt, BC, or C horizon), and at a depth intermediate between the shallow and deep measurements (Bt, BC, or C horizon) with a constant head permeameter. The K_s of individual horizons ranged from 1 × 10^− 8 to 2 × 10^− 5 m s^− 1. At six of 10 sites evaluated, clayey upper Bt horizons had higher K_s than deeper horizons with less clay. This difference was attributed to weaker structure in the deeper BC horizons. Structural differences did not explain all variation in K_s with depth, however. Other soil and landscape properties including parent material composition, colluvium on lower slope positions, C horizon cementation, and depth of soil development also affected K_s of horizons in these soils and should be used to better estimate K_s.     

Temporal denitrification patterns in different horizons of two riparian soils

The dynamics of biological denitrification in riparian soil is still poorly understood. We studied the spring‐time pattern of denitrifying enzyme activity (DEA) and the rate of denitrification (DNT) in two hydromorphic riparian soils, one a mollic Gleysol and the other a terric Histosol. The average DEA ranged from 73 to 1232 ng N g^?1 hour^?1, and DNT ranged from 4 to 36 ng N g^?1 hour^?1. Both DEA and DNT diminished with increasing depth in both soil types. This decrease corresponded to a decrease in total and K₂SO₄‐extractable organic carbon and K₂SO₄‐extractable mineral nitrogen. The DEA and DNT differed in their dynamics. The former had no evident pattern in subsurface horizons but increased with temperature at the end of spring in surface and structural horizons. The DNT diminished as the soil dried in the mollic Gleysol when the water table fell. In the terric Histosol, the water table was still too high at the end of spring to affect the DNT. The results suggest that the vertical pattern of denitrification is related to that of organic carbon content. This organic carbon content determines biological activity and the supply of carbon and nitrous oxides. In biologically active horizons temperature drives the dynamics of DEA, whereas soil moisture drives the dynamics of DNT. Our results show the importance of the dynamic soil–water relationship in controlling denitrification within the riparian zone.     

The Effect of Fire on Mercury Cycling in the Soils of Forested Watersheds: Acadia National Park,Maine, U.S.A.

This study compares mercury (Hg) and methylmercury (MeHg) distribution in the soils of two forested stream watersheds at Acadia National Park, Maine, U.S.A. Cadillac Brook watershed, which burned in 1947, has thin soils and predominantly deciduous vegetation. It was compared to the unburned Hadlock Brook watershed, with thicker soil and predominantly coniferous vegetation. Soils in both watersheds were primarily well drained. The fire had a significant impact on the Cadillac watershed, by raising the soil pH, altering the vegetation, and reducing carbon and Hg pools. Total Hg content was significantly higher (P > 0.05) in Hadlock soils (0.18 kg Hg ha^-1) compared to Cadillac soils (0.13 kg Hg ha^-1). Hadlock O horizon had an average Hg concentration of 134±48 ng Hg g^-1 dry weight, compared to 103±23 ng Hg g^-1 dry weight in Cadillac O horizon. Soil pH was significantly higher in all soil horizons at Cadillac compared to Hadlock soils. This difference was especially significant in the O horizon, where Cadillac soils had an average pH of 3.41±0.22 compared to Hadlock soils with an average pH of 2.99±0.13.To study the mobilization potential of Hg in the O horizons of the two watersheds, batch adsorption experiments were conducted, and the results were modeled using surface complexation modeling. The results of Hg adsorption experiments indicated that the dissolved Hg concentration was controlled by the dissolved organic carbon (DOC) concentration. The adsorption isotherms suggest that Hg is more mobile in the O horizon of the unburned Hadlock watershed because of higher solubility of organic carbon resulting in higher DOC concentrations in that watershed.Methylmercury concentrations, however, were consistently higher in the burned Cadillac O horizon (0.20±0.13 ng Hg g^-1 dry weight) than in the unburned Hadlock O horizon (0.07±0.07 ng Hg g^-1 dry weight). Similarly, Cadillac soils possessed a higher MeHg content (0.30 g MeHg ha^-1) than Hadlock soils (0.16 g MeHg ha^-1). The higher MeHg concentrations in Cadillac soils may reflect generally faster rates of microbial metabolism due to more rapid nutrient cycling and higher soil pH in the deciduous forest. In this research, we have shown that the amount of MeHg is not a function of the total pool of Hg in the watershed. Indeed, MeHg was inversely proportional to total Hg, suggesting that landscape factors such as soil pH, vegetation type, or land use history (e.g., fire) may be the determining factors for susceptibility to high Hg in biota.     

Liming effects on some chemical and biological parameters of soil (spodosols and histosols) in a hardwood forest watershed

Acidic lakes and streams can be restored with base application (usually limestone) provided that the base does not wash out before the benefits of alkalization can be realized; liming soils of the adjoining watershed may be an alternative approach. This study was conducted to provide a scientific basis for soil liming. Plots (50 m²) with different limestone dosages (e.g. 0, 5, 10 or 15 Mg CaCO₃ ha^–1) were established on each of two different soils (a Spodosol and a Histosol) in the Woods Lake watershed of the Adirondack Park Region of New York, USA. Six months after soil liming much of the added limestone was still present in both the Spodosol and in the Histosol. Ten months after soil liming results indicated that: (1) soil pH increased (> 1 unit) but mostly in the top 1 cm; (2) net N mineralization increased from 9.6 to ca. 15 µg N g^–1 d ^–1 and nitrification increased from 2.8 to ca. 8 µg N g^–1 d^–1; (3) denitrification was not affected (98 µg N g^–1 d^–1);(4) CO₂ production potential decreased in the surface soil and as a function of limestone dosage (60 to 6 µmol g^–1 d^–1); and (5) soluble SO _inf4 ^sup2– concentrations in the Histosol were not affected (105 µmol L^–1). Liming acidic forest soils with > 5 Mg CaCO₃ ha^–1 may increase the soil's acid neutralizing capacity, which could provide long-term benefits for surface water acidification.     

Enzymatic activities and microbial communities in an Antarctic dry valley soil: Responses to C and N supplementation

The soils of the Antarctic dry valleys are exposed to extremely dry and cold conditions. Nevertheless, they contain small communities of micro-organisms that contribute to the biogeochemical transformations of the bioelements, albeit at slow rates. We have determined the dehydrogenase, β-glucosidase, acid and alkaline phosphatase and arylsulphatase activities and the rates of respiration (CO₂ production) in laboratory assays of soils collected from a field experiment in an Antarctic dry valley. The objective of the field experiment was to test the responses of the soil microbial community to additions of C and N in simple (glucose and NH₄Cl) and complex forms (glycine and lacustrine detritus from the adjacent lake comprising principally cyanobacterial necromass). The soil samples were taken 3 years after the experimental treatments had been applied. In unamended soil, all enzyme activities and respiration were detected indicating that the enzymatic capacity to mineralize organic C, P and S compounds existed in the soil, despite the very low organic matter content. Relative to the control (unamended soil), respiration was significantly increased by all the experimental additions of C and N except the smallest NH₄Cl addition (1 mg N g⁻¹ soil) and the smallest detritus addition (1.5 mg C g⁻¹ soil and 0.13 mg N g⁻¹ soil). The activities of all enzymes except dehydrogenase were increased by C and combined large C (10 mg C g⁻¹ soil) and N additions, but either unchanged or diminished by addition of either N only or N (up to 10 mg N g⁻¹ soil) with only small C (1 mg C g⁻¹ soil) additions in the form of glucose and NH₄Cl. This suggests that in the presence of a large amount of N, the C supply for enzyme biosynthesis was limited. When normalized with respect to soil respiration, only arylsulphatase per unit of respiration showed a significant increase with C and N additions as glucose and NH₄Cl, consistent with S limitation when C and N limitations have been alleviated. Based on the positive responses of enzyme activity, detritus appeared to provide either conditions or resources which led to a larger biological response than a similar amount of C and more N added in the form of defined compounds (glucose, NH₄Cl or glycine). Assessment of the soil microbial community by ester-linked fatty acid (ELFA) analysis provided no evidence of changes in the community structure as a result of the C and N supplementation treatments. Thus the respiration and enzyme activity responses to supplementation occurred in an apparently structurally stable or unresponsive microbial community.     

C and N turnover in structurally intact soils of different texture

The turnover of native and applied C and N in undisturbed soil samples of different texture but similar mineralogical composition, origin and cropping history was evaluated at −10 kPa water potential. Cores of structurally intact soil with 108, 224 and 337 g clay kg⁻¹ were horizontially sliced and ¹⁵N-labelled sheep faeces was placed between the two halves of the intact core. The cores together with unamended treatments were incubated in the dark at 20 °C and the evolution of CO₂-C determined continuously for 177 d. Inorganic and microbial biomass N and ¹⁵N were determined periodically. Net nitrification was less in soil amended with faeces compared with unamended soil. When adjusted for the NO₃-N present in soil before faeces was applied, net nitrification became negative indicating that NO₃-N had been immobilized or denitrified. The soil most rich in clay nitrified least N and ¹⁵N. The amounts of N retained in the microbial biomass in unamended soils increased with clay content. A maximum of 13% of the faeces ¹⁵N was recovered in the microbial biomass in the amended soils. CO₂-C evolution increased with clay content in amended and unamended soils. CO₂-C evolution from the most sandy soil was reduced due to a low content of potentially mineralizable native soil C whereas the rate constant of C mineralization rate peaked in this soil. When the pool of potentially mineralizable native soil C was assumed proportional to volumetric water content, the three soils contained similar proportions of potentially mineralizable native soil C but the rate constant of C mineralization remained highest in the soil with least clay. Thus although a similar availability of water in the three soils was ensured by their identical matric potential, the actual volume of water seemed to determine the proportion of total C that was potentially mineralizable. The proportion of mineralizable C in the faeces was similar in the three soils (70% of total C), again with a higher rate constant of C mineralization in the soil with least clay. It is hypothesized that the pool of potentially mineralizable C and C rate constants fluctuate with the soil water content.