Influence of nitrogen on atrazine and 2, 4 dichlorophenoxyacetic acid mineralization in blackwater and redwater forested wetland soils

 Microcosms were used to determine the influence of N additions on active bacterial and fungal biomass, atrazine and dichlorophenoxyacetic acid (2,4-D) mineralization at 5, 10 and 15 weeks in soils from blackwater and redwater wetland forest ecosystems in the northern Florida Panhandle. Active bacterial and fungal biomass was determined by staining techniques combined with direct microscopy. Atrazine and 2,4-D mineralization were measured radiometrically. Treatments were: soil type, (blackwater or redwater forested wetland soils) and N additions (soils amended with the equivalent of 0, 200 or 400 kg N ha^–1 as NH₄NO₃). Redwater soils contained higher concentrations of C, total N, P, K, Ca, Mn, Fe, B and Zn than blackwater soils. After N addition and 15 weeks of incubation, active bacterial biomass in redwater soils was lower when N was added. Active bacterial biomass in blackwater soils was lower when 400 kg N ha^–1, but not when 200 kg N ha^–1, was added. Active fungal biomass in blackwater soils was higher when 400 kg N ha^–1, but not when 200 kg N ha^–1, was added. Active fungal biomass in redwater soils was lower when 200 kg N ha^–1, but not when 400 kg N ha^–1, was added. After 15 weeks of incubation 2,4-D degradation was higher in redwater wetland soils than in blackwater soils. After 10 and 15 weeks of incubation the addition of 200 or 400 kg N ha^–1 decreased both atrazine and 2,4-D degradation in redwater soils. The addition of 400 kg N ha^–1 decreased 2,4-D degradation but not atrazine degradation in blackwater soils after 10 and 15 weeks of incubation. High concentrations of N in surface runoff and groundwater resulting from agricultural operations may have resulted in the accumulation of N in many wetland soils. Large amounts of N accumulating in wetlands may decrease mineralization of toxic agricultural pesticides. Received: 26 June 1998     

Influence of ectomycorrhizal mat soils on lignin and cellulose degradation

Summary The ectomycorrhizal fungus Hysterangium setchellii (Fisher) forms extensive hyphal mats at the soillitter interface with the roots of the host tree Douglas fir Pseudotsuga menziesii [(Mirb.) Franco]. Microbial biomass, and lignin and cellulose decomposition rates were measured seasonally for 1 year, using ¹⁴C techniques in ectomycorrhizal mat soils and adjacent non-mat soils in a second-growth Douglas fir forest. The microbial biomass and cellulose degradation rates were 3–6 times higher in ectomycorrhizal mat soils than in adjacent nonmat soils. Lignin degradation rates were higher in ectomycorrhizal mat soils than adjacent non-mat soils. Our data suggest that the ectomycorrhizal fungus H. setchellii provides a microenvironment with increased microbiological activity which results in faster lignin and cellulose decomposition.     

The role of lignin and cellulose in the carbon-cycling of degraded soils under semiarid climate and their relation to microbial biomass

A high level of biological degradation is usually observed in soils under semiarid climate where the low inputs of vegetal debris constraint the development of microbiota. Among vegetal inputs, cellulose and lignin are dominant substrates but their assimilation by the microbial community of semiarid soils is yet not understood. In the present study, ¹³C-labeled cellulose and ¹³C-labeled lignin (75 μg ¹³C g⁻¹ soil) were added to two semiarid soils with different properties and degradation level. Abanilla soil is a bare, highly degraded soil without plant cover growing on it and a total organic C content of 5.0 g kg⁻¹; Santomera soil is covered by plants (20% coverage) based on xerophytic shrubs and has a total organic C content of 12.0 g kg⁻¹. The fate of added carbon was evaluated by analysis of the carbon isotope signature of bulk soil-derived carbon and extractable carbon fractions (water and sodium-pyrophosphate extracts). At long-term (120 days), we observed that the stability of cellulose- and lignin-derived carbon was dependent on their chemical nature. The contribution of lignin-derived carbon to the pool of humic substances was higher than that of cellulose. However, at short-term (30 days), the mineralization of the added substrates was more related to the degradation level of soils (i.e. microbial biomass). Stable isotope probing (SIP) of phospholipid fatty acids (PLFA-SIP) analysis revealed that just a minor part of the microbial community assimilated the carbon derived from cellulose and lignin. Moreover, the relative contribution of each microbial group to the assimilation of lignin-derived carbon was different in each soil.     

Nitrogen mineralization and microbial activity in permanent pastures amended with nitrogen fertilizer or dung

 Gross rates of soil processes and microbial activity were measured in two grazed permanent pasture soils which had recently been amended with N fertilizer or dung. ¹⁵N studies of rates of soil organic matter turnover showed gross N mineralization was higher, and gross N immobilization was lower, in a long-term fertilized soil than in a soil which had never received fertilizer N. Net mineralization was also found to be higher in the fertilized soil: a consequence of the difference between the opposing N turnover processes of N mineralization and immobilization. In both soils without amendments the soil microbial biomass contents were similar, but biomass activity (specific respiration) was higher in the fertilized soil. Short-term manipulation of fertilizer N input, i.e. adding N to unfertilized soil, or witholding N from previously fertilized soil, for one growing season, did not affect gross mineralization, immobilization or biomass size and activity. Amendments of dung had little effect on gross mineralization, but there was an increase in immobilization in both soils. Total biomass also increased under dung in the unfertilized soil, but specific respiration was reduced, suggesting changes in the composition of the biomass. Dung had a direct effect on the microbial biomass by temporarily increasing available soil C. Prolonged input of fertilizer N increases soil C indirectly as a result of enhanced plant growth, the effect of which may not become evident within one seasonal cycle. Received: 18 December 1998     

Carbon additions increase nitrogen availability in northern hardwood forest soils

 The effects of acetate additions to northern hardwood forest soils on microbial biomass carbon (C) and nitrogen (N) content, soil inorganic N levels, respirable C and potential net N mineralization and nitrification were evaluated. The experiment was relevant to a potential watershed-scale calcium (Ca) addition that aims to replace Ca depleted by long-term exposure to acid rain. One option for this addition is to use calcium-magnesium (Mg) acetate, a compound that is inexpensive and much more readily soluble than the Ca carbonate that is generally used for large-scale liming. Field plots were treated with sodium (NA) acetate, Na bicarbonate or water (control) and were sampled (forest floor – Oe and Oa combined) 2, 10 and 58 days following application. It was expected that the addition of C would lead to an increase in biomass C and N and a decrease in inorganic N. Instead, we observed no effect on biomass C, a decline in biomass N and an increase in N availability. One possible explanation for our surprising results is that the C addition stimulated microbial activity but not growth. A second, and more likely, explanation for our results is that the C addition did stimulate microbial growth and activity, but there was no increase in microbial biomass due to predation of the new biomass by soil fauna. The results confirm the emerging realization that the effects of increases in the flow of C to soils, either by deliberate addition or from changes in atmospheric CO₂, are more complex than would be expected from a simple C : N ratio analysis. Evaluations of large-scale manipulations of forest soils to ameliorate effects of atmospheric deposition or to dispose of wastes should consider microbial and faunal dynamics in considerable detail. Received: 13 March 1998     

The influence of nitrogen on atrazine and 2,4-dichlorophenoxyacetic acid mineralization in grassland soils

The influence of fertilizer N on the mineralization of atrazine [2-chloro-4(ethylamino)-6(isopropylamino)-s-triazine] and 2,4-D (2,4-dichlorophenoxyacetic acid) in soils was assessed in microcosms using radiometric techniques. N equivalent to 0, 250, and 500 kg N as NH₄NO₃ ha^-1 was added to three grassland soils. Compared to the control, the 250- and 500-kg treatments suppressed mineralization of atrazine by 75 and 54%, respectively, and inhibited mineralization of 2,4-D by 89 and 30%, respectively. Active fungal biomass responded to the N treatments in an opposite manner to herbicide mineralization. Compared to the control, the 250- and 500-kg treatments increased the active fungal biomass by more than 300 and 30%, respectively. These results agree with other observations that N can suppress the decomposition of resistant compounds but stimulate the primary growth of fungi. The degree of suppression was not related to the amount of N added nor to the inherent soil N levels before treatment. The interaction between the N additions and the active fungal biomass in affecting herbicide mineralization suggests that N may alter microbial processes and their use of C sources and thus influence rates of herbicide degradation in the field.     

Effect of cropping systems on nitrogen mineralization in soils

 Understanding the effect of cropping systems on N mineralization in soils is crucial for a better assessment of N fertilizer requirements of crops in order to minimize nitrate contamination of surface and groundwater resources. The effects of crop rotations and N fertilization on N mineralization were studied in soils from two long-term field experiments at the Northeast Research Center and the Clarion-Webster Research Center in Iowa that were initiated in 1979 and 1954, respectively. Surface soil samples were taken in 1996 from plots of corn (Zea mays L.), soybean (Glycine max (L.) Merr.), oats (Avena sativa L.), or meadow (alfalfa) (Medicago sativa L.) that had received 0 or 180 kg N ha^–1 before corn and an annual application of 20 kg P and 56 kg K ha^–1. N mineralization was studied in leaching columns under aerobic conditions at 30  °C for 24 weeks. The results showed that N mineralization was affected by cover crop at the time of sampling. Continuous soybean decreased, whereas inclusion of meadow increased, the amount of cumulative N mineralized. The mineralizable N pool (N _o) varied considerably among the soil samples studied, ranging from 137 mg N kg^–1 soil under continuous soybean to >500 mg N kg^–1 soil under meadow-based rotations, sampled in meadow. The results suggest that the N _o and/or organic N in soils under meadow-based cropping systems contained a higher proportion of active N fractions. Received: 10 February 1999     

Short- and long-term effects of nitrogen fertilization on methane oxidation in three Swedish forest soils

 Under normal conditions, CH₄, one of the most important greenhouse gases, is subject to biological oxidation in forest soils. However, this process can be negatively affected by N amendment. The reported experiment was conducted in order to study the short- and long-term effects of N amendment on CH₄ oxidation in pine (Pinus sylvestris L.) forest soils. Soil samples were taken from three experimental sites, two of which had been amended with N once, over 20 years earlier, while the third had been amended 3 weeks earlier. The soil samples were incubated fresh at 15  °C at ambient CH₄ concentrations (ca. 1.8 ppmv CH₄). The variation in CH₄-turnover rates was high within the treatments: CH₄ was produced [up to 22.6 pmol CH₄ g dry wt. soil^–1 h^–1] in samples from the recently amended site, whereas it was consumed at high rates (up to 431 pmol CH₄ g dry wt. soil^–1 h^–1) in samples from the plot that had received the highest N amendment 27 years before sampling. Although no significant differences were found between N treatments, in the oldest plots there was a correlation between consumption of atmospheric CH₄ and the total C content at a depth of 7.5–15 cm in the mineral soil (r ²=0.74). This indicates that in the long-term, increased C retention in forest soils following N amendment could lead to increased CH₄ oxidation. Received: 3 September 1997     

Soluble organic nitrogen in agricultural soils

 The existence of soluble organic forms of N in rain and drainage waters has been known for many years, but these have not been generally regarded as significant pools of N in agricultural soils. We review the size and function of both soluble organic N extracted from soils (SON) and dissolved organic N present in soil solution and drainage waters (DON) in arable agricultural soils. SON is of the same order of magnitude as mineral N and of equal size in many cases; 20–30 kg SON-N ha^–1 is present in a wide range of arable agricultural soils from England. Its dynamics are affected by mineralisation, immobilisation, leaching and plant uptake in the same way as those of mineral N, but its pool size is more constant than that of mineral N. DON can be sampled from soil solution using suction cups and collected in drainage waters. Significant amounts of DON are leached, but this comprises only about one-tenth of the SON extracted from the same soil. Leached DON may take with it nutrients, chelated or complexed metals and pesticides. SON/DON is clearly an important pool in N transformations and plant uptake, but there are still many gaps in our understanding. Received: 10 June 1999     

Short-term effects of nitrogen on methane oxidation in soils

 The short-term effects of N addition on CH₄ oxidation were studied in two soils. Both sites are unfertilized, one has been under long-term arable rotation, the other is a grassland that has been cut for hay for the past 125 years. The sites showed clear differences in their capacity to oxidise CH₄, the arable soil oxidised CH₄ at a rate of 0.013 μg CH₄ kg^–1 h^–1 and the grassland soil approximately an order of magnitude quicker. In both sites the addition of (NH₄)₂SO₄ caused an immediate reduction in the rate of atmospheric CH₄ oxidation approximately in inverse proportion to the amount of NH₄ ⁺ added. The addition of KNO₃ caused no change in the rate of CH₄ oxidation in the arable soil, but in the grassland soil after 9 days the rate of CH₄ oxidation had decreased from 0.22 μg CH₄ kg^–1 h^–1 to 0.13 μg CH₄ kg^–1 h^–1 in soil treated with the equivalent of 192 kg N ha^–1. A ¹⁵N isotopic dilution technique was used to investigate the role of nitrifiers in regulating CH₄ oxidation. The arable soil showed a low rate of gross N mineralisation (0.67 mg N kg^–1 day^–1), but a relatively high proportion of the mineralised N was nitrified. The grassland soil had a high rate of gross N mineralisation (18.28 mg N kg^–1 day^–1), but negligible nitrification activity. It is hypothesised that since there was virtually no nitrification in the grassland soil then CH₄ oxidation at this site must be methanotroph mediated. Received: 31 October 1997     

Influence of the presence of nitrite and nitrate in soil on maize biomass production, nitrogen immobilization and nitrogen recovery

 When comparing nitrite (NO₂ ^–) and nitrate (NO₃ ^–) toxicity to maize (Zea mays L.) growth, it is important to know the fate of applied nitrogen (N). A pot experiment, using potassium nitrite (K¹⁵NO₂) and potassium nitrate (K¹⁵NO₃) was conducted to determine the fate of N (0, 75, 150, and 225 mg N kg^–1 soil) applied to a sandy loam soil collected from Gistel (Belgium). The total dry weight of the plants treated with NO₂ ^– was lower than that of the plants treated with NO₃ ^– at 15 and 26 days after N application (harvest 1 and harvest 2, respectively). Shoot and root biomass reduction started at a relatively low NO₂ ^– application rate (75 mg NO₂ ^–-N kg^–1). Biomass reduction increased, at both harvests with increasing amounts of NO₂ ^– to more than 55% at the highest application rate (225 mg NO₃ ^–-N kg^–1). In the NO₃ ^– treatment, a reduction of 16% in total plant dry biomass was recorded only at the highest application rate (225 mg NO₂ ^–-N kg^–1), at both harvest times. The ¹⁵N plant uptake (shoots plus roots) at harvest 1 decreased with increasing N application rates of both N forms (KNO₂ and KNO₃). Twenty-six days after the N application, the total ¹⁵N taken up by the plant increased in all treatments in comparison with 15 days after the N application. However, only at higher rates of N application (150 and 225 mg N kg^–1) was the ¹⁵N uptake by the NO₂ ^– fed plants significantly lower than by the NO₃ ^– fed plants. The percentage of immobilized N from the applied N was low (0–17.7%) at both harvests, irrespective of the N source. However, with relatively low N application rates (75 mg N kg^–1), the immobilized N in the soil decreased with time. This may be due to the re-mineralization of the applied N. The percentage of inorganic ¹⁵N in the soil in NO₂ ^– treatments was slightly lower than in equivalent doses of NO₃ ^–. This might be due to higher losses of N as N-oxides. Unaccounted for N from the applied N ranged from 21% to 52% for the NO₂ ^– treatments and from 3% to 38% for the NO₃ ^– treatments. Received: 17 July 1997     

Gross nitrogen mineralization and nitrification rates and their relationships to enzyme activities and the soil microbial biomass in soils treated with dairy shed effluent and ammonium fertilizer at different water potentials

 Gross N mineralization and nitrification rates and their relationships to microbial biomass C and N and enzyme (protease, deaminase and urease) activities were determined in soils treated with dairy shed effluent (DSE) or NH₄ ⁺ fertilizer (NH₄Cl) at a rate equivalent to 200 kg N ha^–1 at three water potentials (0, –10 and –80 kPa) at 20  °C using a closed incubation technique. After 8, 16, 30, 45, 60 and 90 days of incubation, sub-samples of soil were removed to determine gross N mineralization and nitrification rates, enzyme activities, microbial biomass C and N, and NH₄ ⁺ and NO₃ ^– concentrations. The addition of DSE to the soil resulted in significantly higher gross N mineralization rates (7.0–1.7 μg N g^–1 soil day^–1) than in the control (3.8–1.2 μg N g^–1 soil day^–1), particularly during the first 16 days of incubation. This increase in gross mineralization rate occurred because of the presence of readily mineralizable organic substrates with low C : N ratios, and stimulated soil microbial and enzymatic activities by the organic C and nutrients in the DSE. The addition of NH₄Cl did not increase the gross N mineralization rate, probably because of the lack of readily available organic C and/or a possible adverse effect of the high NH₄ ⁺ concentration on microbial activity. However, nitrification rates were highest in the NH₄Cl-treated soil, followed by DSE-treated soil and then the control. Soil microbial biomass, protease, deaminase and urease activities were significantly increased immediately after the addition of DSE and then declined gradually with time. The increased soil microbial biomass was probably due to the increased available C substrate and nutrients stimulating soil microbial growth, and this in turn resulted in higher enzyme activities. NH₄Cl had a minimal impact on the soil microbial biomass and enzyme activities, possibly because of the lack of readily available C substrates. The optimum soil water potential for gross N mineralization and nitrification rates, microbial and enzyme activities was –10 kPa compared with –80 kPa and 0 kPa. Gross N mineralization rates were positively correlated with soil microbial biomass N and protease and urease activities in the DSE-treated soil, but no such correlations were found in the NH₄Cl-treated soil. The enzyme activities were also positively correlated with each other and with soil microbial biomass C and N. The forms of N and the different water potentials had a significant effect on the correlation coefficients. Stepwise regression analysis showed that protease was the variable that most frequently accounted for the variations of gross N mineralization rate when included in the equation, and has the potential to be used as one of the predictors for N mineralization. Received: 10 March 1998     

Plant lignin and nitrogen contents control carbon dioxide production and nitrogen mineralization in soils incubated with Bt and non-Bt corn residues

Bt (Bacillus thuringiensis) corn is reported to produce lignin-rich residues, compared to non-Bt (NBt) corn, suggesting it is more resistant to decomposition. As the Bt gene is expressed selectively in stem and leaf tissue, it could affect lignin distribution in corn, which naturally has greater lignin content in roots than in stems and leaves. Our objective was to evaluate the effects of corn plant components, the Bt gene and elevated-lignin inputs on decomposition. Roots, stems and leaves from Bt corn and NBt corn isolines enriched with ¹³C and ¹⁵N were finely ground and mixed separately with soil, then incubated at 20 °C for 36 weeks. The effect of elevated lignin on decomposition was tested by adding a commercial lignin source (indulin lignin) to half of the samples. In addition to weekly CO₂ analysis and regular measurement of N mineralization, the degree of lignin degradation was evaluated at 1 and 36 weeks from the acid to aldehyde ratio (Ad/Al) of vanillyl and syringyl lignin-derived phenols. The CO₂ production and N mineralization was lower in root-amended soils than stem- and leaf-amended soils. The Bt genetic modification increased CO₂ production from stem-amended soils (P < 0.05) and decreased N mineralization in root-amended soils. The ¹³C and ¹⁵N results also showed more residue-C and -N retained in soils mixed with NBt stem residues. After 36 weeks leaf- and stem-amended soils with indulin lignin had a lower Ad/Al ratio and were less degraded than soils without exogenous lignin. In conclusion, plant lignin and nitrogen contents were good predictors of CO₂ production and N mineralization potential. Corn roots decomposed more slowly than aboveground components emphasizing the importance of recalcitrant root residues in sustaining the organic matter content of soil.     

Influence of soil compaction on carbon and nitrogen mineralization of soil organic matter and crop residues

 We studied the influence of soil compaction in a loamy sand soil on C and N mineralization and nitrification of soil organic matter and added crop residues. Samples of unamended soil, and soil amended with leek residues, at six bulk densities ranging from 1.2 to 1.6 Mg m^–3 and 75% field capacity, were incubated. In the unamended soil, bulk density within the range studied did not influence any measure of microbial activity significantly. A small (but insignificant) decrease in nitrification rate at the highest bulk density was the only evidence for possible effects of compaction on microbial activity. In the amended soil the amounts of mineralized N at the end of the incubation were equal at all bulk densities, but first-order N mineralization rates tended to increase with increasing compaction, although the increase was not significant. Nitrification in the amended soils was more affected by compaction, and NO₃ ^–-N contents after 3 weeks of incubation at bulk densities of 1.5 and 1.6 Mg m^–3 were significantly lower (by about 8% and 16% of total added N, respectively), than those of the less compacted treatments. The C mineralization rate was strongly depressed at a bulk density of 1.6 Mg m^–3, compared with the other treatments. The depression of C mineralization in compacted soils can lead to higher organic matter accumulation. Since N mineralization was not affected by compaction (within the range used here) the accumulated organic matter would have had higher C : N ratios than in the uncompacted soils, and hence would have been of a lower quality. In general, increasing soil compaction in this soil, starting at a bulk density of 1.5 Mg m^–3, will affect some microbially driven processes. Received: 10 June 1999     

Influence of soil phosphorus status and nitrogen addition on carbon mineralization from 14C-labelled glucose in pasture soils

 This study examines the effect of soil P status and N addition on the decomposition of ¹⁴C-labelled glucose to assess the consequences of reduced fertilizer inputs on the functioning of pastoral systems. A contrast in soil P fertility was obtained by selecting two hill pasture soils with different fertilizer history. At the two selected sites, representing low (LF) and high (HF) fertility status, total P concentrations were 640 and 820 mg kg^–1 and annual pasture production was 4,868 and 14,120 kg DM ha^–1 respectively. Soils were amended with ¹⁴C-labelled glucose (2,076 mg C kg^–1 soil), with and without the addition of N (207 mg kg^–1 soil), and incubated for 168 days. During incubation, the amounts of ¹⁴CO₂ respired, microbial biomass C and ¹⁴C, microbial biomass P, extractable inorganic P (P_i) and net N mineralization were determined periodically. Carbon turnover was greatly influenced by nutrient P availability. The amount of glucose-derived ¹⁴CO₂ production was high (72%) in the HF and low (67%) in the LF soil, as were microbial biomass C and P concentrations. The ¹⁴C that remained in the microbial biomass at the end of the 6-month incubation was higher in the LF soil (15%) than in the HF soil (11%). Fluctuations in P_i in the LF soil during incubation were small compared with those in HF soil, suggesting that P was cycling through microbial biomass. The concentrations of P_i were significantly greater in the HF samples throughout the incubation than in the LF samples. Net N mineralization and nitrification rates were also low in the LF soils, indicating a slow turnover of microorganisms under limited nutrient supply. Addition of N had little effect on biomass ¹⁴C and glucose utilization. This suggests that, at limiting P fertility, C turnover is retarded because microbial biomass becomes less efficient in the utilization of substrates. Received: 18 October 1999     

Soil microbial biomass and mineralization of carbon and nitrogen in ecological, integrated and conventional forage and arable cropping systems

 In a cropping systems experiment in southeastern Norway, ecological (ECO), integrated (INT) and conventional (CON) forage (FORAGE) and arable (ARABLE) model farms were compared. After 5 experimental years, topsoil was sampled in spring from spring grain plots and incubated for 449 days at controlled temperature (15  °C) and moisture content (50% water-holding capacity). There were no detectable differences between model farms in terms of total soil C or N. For INT and CON, however, values of microbial biomass C and N, microbial quotient (C_mic/C_org), and C and N mineralization were, or tended to be, higher for FORAGE than for ARABLE. For the ECO treatment, values were similar for FORAGE and ARABLE and did not differ significantly from that of CON-FORAGE. For INT and CON, the metabolic quotient (qCO₂) was lower for FORAGE than for ARABLE. Again, for the ECO treatment, values were similar for FORAGE and ARABLE and did not differ significantly from that of CON-FORAGE. We estimated the sizes of conceptual soil organic matter pools by fitting a decomposition model to biomass and mineralization data. This resulted in a 48% larger estimate for CON-FORAGE than for CON-ARABLE of physically protected biomass C. For physically protected organic C the difference was 42%. Moreover, the stability of soil aggregates against artificial rainfall was substantially greater for CON-FORAGE than for CON-ARABLE. On this basis, we hypothesized that the lower qCO₂ values in the FORAGE soils were mainly caused by a smaller proportion of active biomass due to enclosure of microorganisms within aggregates. Altogether, our results indicated a poorer inherent soil fertility in ARABLE than in FORAGE rotations, but the difference was small or absent in the ECO system, probably owing to the use of animal and green manures and reduced tillage intensity in the ECO-ARABLE rotation. Received: 28 October 1998     

Influence of N and non-N salts on atmospheric methane oxidation by upland boreal forest and tundra soils

 The short-term (24 h) and medium-term (30 day) influence of N salts (NH₄Cl, NaNO₃ and NaNO₂) and a non-N salt (NaCl) on first-order rate constants, k (h^–1) and thresholds (C_Th) for atmospheric CH₄ oxidation by homogenized composites of upland boreal forest and tundra soils was assessed at salt additions ranging to 20 μmol g^–1 dry weight (dw) soil. Additions of NH₄Cl, NaNO₃ and NaCl to 0.5 μmol g^–1 dw soil did not significantly decrease k relative to watered controls in the short term. Higher concentrations significantly reduced k, with the degree of inhibition increasing with increasing dose. Similar doses of NH₄Cl and NaCl gave comparable decreases in k relative to controls and both soils showed low native concentrations of NH₄ ⁺-N (≤1 μmol g^–1dw soil), suggesting that the reduction in k was due primarily to a salt influence rather than competitive inhibition of CH₄ oxidation by exogenous NH₄ ⁺-N or NH₄ ⁺-N released through cation exchange. The decrease in k was consistently less for NaNO₃ than for NH₄Cl and NaCl at similar doses, pointing to a strong inhibitory effect of the Cl^– counter-anion. Thresholds for CH₄ oxidation were less sensitive to salt addition than k for these three salts, as significant increases in C_Th relative to controls were only observed at concentrations ≥1.0 μmol g^–1 dw soil. Both soils were more sensitive to NaNO₂ than to other salts in the short term, showing a significant decrease in k at an addition of 0.25 μmol NaNO₂ g^–1 dw soil that was clearly attributable to NO₂ ^–. Soils showed no recovery from NaCl, NH₄ ⁺-N or NaNO₃ addition with respect to atmospheric CH₄ oxidation after 30 days. However, soils amended with NaNO₂ to 1.0 μmol NaNO₂ g^–1 dw showed values of k that were not significantly different from controls. Recovery of CH₄-oxidizing ability was due to complete oxidation of NO₂ ^–-N to NO₃ ^–-N. Analysis of soil concentrations of N salts necessary to inhibit atmospheric CH₄ oxidation and regional rates of N deposition suggest that N deposition will not decrease the future sink strength of upland high-latitude soils in the atmospheric CH₄ budget. Received: 30 April 1999     

Effect of microbial nitrogen immobilization during the growth period on the availability of nitrogen fertilizer for winter cereals

 Pot and field experiments were conducted to determine microbial immobilization of N fertilizer during growth periods of winter wheat and winter barley. In a pot experiment with winter wheat, Ca(¹⁵NO₃)₂ was applied at tillering [Zadok's growth stage (GS) 25)], stem elongation (GS 31) and ear emergence (GS 49). Rates of 100 mg N pot^–1, 200 mg N pot^–1 or 300 mg N pot^–1 were applied at each N application date. At crop maturity, ¹⁵N-labelled fertilizer N immobilization was highest at the highest N rate (3×300 mg N pot^–1). For each N-rate treatment about 50% of the total immobilized fertilizer N was immobilized from the first N dressing, and 30% and 20% of the total ¹⁵N immobilized was derived from the second and third applications, respectively. In field trials with winter wheat (three sites) and winter barley (one site) N was applied at the same growth stages as for the pot trial. N was also applied to fallow plots, but only at GS 25. N which was not recovered (neither in crops nor in soil mineral N pools) was considered to represent net immobilized N. A clear effect of N rate (51–255 kg N ha^–1) on net N immobilization was not found. The highest net N immobilization was found for the period between GS 25 (March) and GS 31 (late April) which amounted to 54–97% of the total net N immobilized at harvest (July/August). At GS 31, non-recovered N was found to be of similar magnitude for cropped and fallow plots, indicating that C from roots did not affect net N immobilization. Microbial biomass N (N_mic) was determined for cropped plots at GS 31. Although N_mic tended to be higher in fertilized than in unfertilized plots, fertilizer-induced increases in N_mic and net N immobilization were poorly correlated. It can be concluded that microbial immobilization of fertilizer N is particularly high after the first N application when crop growth and N uptake are low. Received: 6 July 1999     

Effects of fungal inocula on the decomposition of lignin and structural polysaccharides in Pinus sylvestris litter

 Litter bags containing sterile Scots pine (Pinus sylvestris) needles (19.8% lignin, 26.5% cellulose and 0.34% N) were inoculated with two species of fungi in the laboratory and then placed in the litter layer of a pine plantation. Marasmius androsaceus, which can degrade lignocellulose, was initially displaced by other fungal colonisers and was not detected in the litter after 2–3 months; but was re-isolated from the needles after 12 months. Trichoderma viride, which is a cellulolytic species and also antagonistic to other fungi, dominated the litter throughout the experiment. The control litter was naturally colonised by litter fungi. After 12 months, mass losses were similar at 52% for M. androsaceus and 48% for T. viride, compared with 36% for the control litter colonised by a more complex fungal community. Lignin concentrations increased with time in control litter and with T. viride because mass losses of carbohydrates were greater than those of lignin. Litter inoculated with M. androsaceus showed significant lignin decomposition throughout the experiment but cellulose concentrations showed a proportional increase in the first 6 months, suggesting that the fungus was preferentially exploiting hemicellulose and non-structural carbohydrates. Analysis of TFA-extractable sugars (mainly from hemicellulose) and CuO-derived phenylpropanoid moieties from lignin confirmed the differential patterns of resource decomposition which were not evident from total mass losses. During the initial stages of decomposition, T. viride was as effective in utilising structural polysaccharides as the complex fungal community in the control litter. Furthermore, M. androsaceus not only exhibited unexpectedly low cellulolytic activity but also facilitated lignin depolymerisation after the fungus was no longer detectable in the litter. The pre-inoculation of litter with these two fungal species therefore affected the overall dynamics of decomposition at a biochemical level. This study illustrates the importance of understanding the effects and interactions of specific fungi, rather than assumptions about the functional competence of diverse communities, on the processes of litter decomposition. Received: 5 July 2000     

Mineralization of nitrogen from decomposing leaves of multipurpose trees as affected by their chemical composition

 Nitrogen release patterns from seven leguminous trees were determined from 8-week laboratory incubations. The quantities of extractable NH₄ ⁺-N and NO₃ ^– released to the soil to which the leaves had been applied was determined at weekly intervals and was related to the initial N, polyphenol, and lignin concentration of the leaves. Cumulative N mineralized was not correlated to initial N, soluble polyphenol and insoluble tannin concentrations, but was correlated to lignin and neutral detergent fibre N (NDF-N) concentrations. The ratios of NDF-N : N (r=0.68 at P<0.05), soluble polyphenol : N (r=0.70 at P<0.05) and (lignin+polyphenol) : N (r=0.75 at P<0.05) were negatively correlated with N release. Total polyphenol content was not a useful predictor of N release, but the reactivity of the polyphenols as measured by their protein-binding capacity can be a useful predictor. In addition to measuring the concentration of polyphenols, their reactivity with proteins must be measured, in order to assess their role in regulating N release. The (lignin+polyphenol) : N ratio could be used to screen leguminous tree leaves for their potential to release N in short-term experiments. This would allow for rapid screening of a large number of trees without detailed and expensive field experimentation. Received: 30 June 1997