Effects of repeated manure and fertilizer phosphorus additions on soil phosphorus dynamics under a soybean-wheat rotation

 Soil P availability and efficiency of applied P may be improved through an understanding of soil P dynamics in relation to management practices in a cropping system. Our objectives in this study were to evaluate changes in plant-available (Olsen) P and in different inorganic P (P_i) and organic P (P₀) fractions in soil as related to repeated additions of manure and fertilizer P under a soybean-wheat rotation. A field experiment on a Typic Haplustert was conducted from 1992 to 1995 wherein the annual treatments included four rates of fertilizer P (0, 11, 22 and 44 kg ha^–1 applied to both soybean and wheat) in the absence and presence of 16 t ha^–1 of manure (applied to soybean only). With regular application of fertilizer P to each crop the level of Olsen P increased significantly and linearly through the years in both manured and unmanured plots. The mean P balance required to raise Olsen P by 1 mg kg^–1 was 17.9 kg ha^–1 of fertilizer P in unmanured plots and 5.6 kg ha^–1 of manure plus fertilizer P in manured plots. The relative sizes of labile [NaHCO₃-extractable P_i (NaHCO₃-P_i) and NaHCO₃-extractable P₀ (NaHCO₃-P₀)], moderately labile [NaOH-extractable P_i (NaOH-P_i) and NaOH-extractable P₀ (NaOH-P₀)] and stable [HCl-extractable P (HCl-P) and H₂SO₄/H₂O₂-extractable P (resisual-P)] P pools were in a 1 : 2.9 : 7.6 ratio. Application of fertilizer P and manure significantly increased NaHCO₃-P_i and -P₀ and NaOH-P_i, and -P₀ fractions and also total P. However, HCl-P and residual-P were not affected. The changes in NaHCO₃-P_i, NaOH-P_i and NaOH-P₀ fractions were significantly correlated with the apparent P balance and were thought to represent biologically dynamic soil P and act as major sources and sinks of plant-available P. Received: 23 October 1997     

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     

Quantifying microbial biomass phosphorus in acid soils

 This study aimed to validate the fumigation-extraction method for measuring microbial biomass P in acid soils. Extractions with the Olsen (0.5 M NaHCO₃, pH 8.5) and Bray-1 (0.03 M NH₄F–0.025 M HCl) extractants at two soil:solution ratios (1 : 20 and 1 : 4, w/v) were compared using eight acid soils (pH 3.6–5.9). The data indicated that the flushes (increases following CHCl₃-fumigation) of total P (P_t) and inorganic P (P_i) determined by Olsen extraction provided little useful information for estimating the amount of microbial biomass P in the soils. Using the Bray-1 extractant at a soil:solution ratio of 1 : 4, and analysing P_i instead of P_t, improves the reproducibility (statistical significance and CV) of the P flush in these soils. In all the approaches studied, the P_i flush determined using the Bray-1 extractant at 1 : 4 provided the best estimate of soil microbial biomass P. Furthermore, the recovery of cultured bacterial and fungal biomass P added to the soils and extracted using the Bray-1 extractant at 1 : 4 was relatively constant (24.1–36.7% and 15.7–25.7%, respectively) with only one exception, and showed no relationship with soil pH, indicating that it behaved differently from added P_i (recovery decreased from 86% at pH 4.6 to 13% at pH 3.6). Thus, correcting for the incomplete recovery of biomass P using added P_i is inappropriate for acid soils. Although microbial biomass P in soil is generally estimated using the P_i flush and a conversion factor (k _P) of 0.4, more reliable estimates require that k _P values are best determined independently for each soil. Received: 3 February 2000     

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     

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     

Phosphorus mineralization and microbial biomass in a Florida Spodosol: effects of water potential, temperature and fertilizer application

 Phosphorus mineralization and microbial biomass were measured in the surface 5 cm of a Spodosol (sandy, siliceous hyperthermic Ultic Alaquod) from north-central Florida. Soils from fertilized and unfertilized plantations of loblolly pine (Pinus taeda L.) were incubated at a range of water potentials (∼0, –3, –8, –10 and –1500 kPa) and temperatures (15  °C, 25  °C and 38  °C) for 14 days and 42 days. Increasing water potential and temperature increased specific P mineralization (mineralization expressed as a percentage of total P) regardless of fertilizer treatment. An increase in water potential from –10 kPa to –0.1 kPa resulted in an increase of between 38% and 239% in the concentration of KCl-extractable inorganic P, depending on incubation temperature and time. An increase in incubation temperature from 15  °C to 38  °C resulted in an increase of between 13% and 53% in KCl-extractable inorganic P. Changes in specific P mineralization with change in water potential or temperature were not affected by fertilizer application. This suggests that, although specific P mineralization was greater in the fertilized soils, environmental control of P mineralization was the same for both treatments. Specific P mineralization was most sensitive when soils were at higher water potentials, and decreased logarithmically to water potentials of between –3 kPa and –8 kPa. Specific P mineralization was relatively insensitive to changes in water potential when water potential was lower than –8 kPa. Microbial biomass C showed no consistent responses to changes of temperature or water potential and was not significantly correlated with specific P mineralization. Our results suggest that field estimates of P mineralization in these Spodosols may be improved by accounting for changes in soil water potential and temperature. Received: 30 October 1997     

Effects of deforestation on phosphorus pools in mountain soils of the Alay Range, Khyrgyzia

 The amount, quality and turnover of soil P is heavily influenced by changes in soil management. The objective of this study was to investigate the effects of deforestation and pasture establishment on the concentrations, forms and turnover rate of soil P in mountain soils of the Alay Range, Khyrgyzia. A sequential extraction was applied to distinguish soil P pools. We used particle-size fractionation to follow the dynamics of different P pools in soils under forest and pasture and ³¹P-NMR spectroscopy to investigate the structure of alkali-soluble P forms. In the A horizons of the forest soils, total soil P concentration was 1093 mg kg^–1, organic P (P_o) representing 46% of the total P. Deforestation followed by pasture establishment not only increased significantly (P<0.01) the total P concentration (1560 mg kg^–1) but also the contribution of P_o to total P was increased by 17%. Pasture soils had significantly higher P pools than forest soils except highly labile inorganic P (P_i NaHCO₃) and primary P_i (P_i HCl_dil). Both in forest and pasture soils stable P increased with decreasing particle size (coarse sand 50%, clay 80% of total P) and primary P decreased with decreasing particle size. Phosphate monoesters and diesters represented 80% of P identified by ³¹P NMR. Low monoester to diester ratios in the alkali extracts of forest and pasture soils indicate low microbial activity. This is consistent with high C/P_o ratios and high stable P_o concentrations in the fine earth of forest and pasture. Received: 10 March 1999     

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     

Influence of nitrogen on cellulose and lignin mineralization in blackwater and redwater forested wetland soils

 Microcosms were used to determine the influence of N additions on active bacterial and active fungal biomass, cellulose degradation and lignin degradation at 5, 10 and 15 weeks in soils from blackwater and redwater wetlands in the northern Florida panhandle. Blackwater streams contain a high dissolved organic C concentration which imparts a dark color to the water and contain low concentrations of nutrients. Redwater streams contain high concentrations of suspended clays and inorganic nutrients, such as N and P, compared to blackwater streams. Active bacterial and fungal biomass was determined by direct microscopy; cellulose and lignin degradation were measured radiometrically. The experimental design was a randomized block. Treatments were: soil type (blackwater or redwater forested wetlands) 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, the active bacterial biomass in redwater soils was lower than in blackwater soils; the active bacterial biomass in blackwater soils was lower when 400 kg N ha^–1, but not when 200 kg N ha^–1, was added. The active fungal biomass in blackwater soils was higher when 400 kg N ha^–1, but not when 200 kg N ha^–1, was added. The active fungal biomass in redwater wetland soils was lower when 200 kg N ha^–1, but not when 400 kg N ha^–1, was added. Cellulose and lignin degradation was higher in redwater than in blackwater soils. After 10 and 15 weeks of incubation, the addition of 200 or 400 kg N as NH₄NO₃ ha^–1 decreased cellulose and lignin degradation in both wetland soils to similar levels. This study indicated that the addition of N may slow organic matter degradation and nutrient mineralization, thereby creating deficiencies of other plant-essential nutrients in wetland forest soils. Received: 7 April 1999     

Mineralization of organic sulfur and its importance as a reservoir of plant-available sulfur in upland soils of north China

 An open incubation technique was used to measure S mineralization in a range of upland soils of north China. Six mineralization patterns were examined, and a soil S-exhaustion experiment with ryegrass (Lolium multiflorum L.) was conducted to investigate the availability of various organic S pools to plants. For all of the 12 soils tested, the release of S as SO₄ ^2– was curvilinear with time, and during a 28-week incubation at 30  °C the amount of S mineralized ranged from 14.0 mg S kg^–1 soil to 37.4 mg S kg^–1 soil. A first-order model and Gompertz model appeared to best describe S mineralization. Examination of the soils after incubation revealed the bulk of the mineralized S was mainly derived from the C-bonded S pool, while the majority of mineralized S under soil S exhaustion by ryegrass was derived from the HI-reducible S pool. Received: 9 July 1998     

Microwave irradiation of soil for routine measurement of microbial biomass carbon

 Microwave irradiation was evaluated as a non-toxic alternate to chloroform fumigation for routine measurement of soil microbial biomass C. Microwave energy was applied to moist soil to disrupt microbial cells. The flush of C released was then measured after extraction or incubation. Microwave irradiation at 800 J g^–1 soil was optimal because this level resulted in an almost instantaneous rise in soil temperature (≥80  °C), an abrupt reduction in microbial activity, maximal release of biomass C, and minimal solubilization of humic substances. Both incubation-CO₂ titration and extraction-colorimetry methods were used on separate 20-g subsamples to compare the labile C in the microwave-treated and untreated soil samples. The incubation-titration method was also used to measure C in chloroform-fumigated soil samples. Averaged across soils, the chloroform fumigation yielded 123.3±5.1 mg CO₂-C kg^–1. Microwave irradiation yielded 93.6±3.9 mg CO₂-C kg^–1 soil determined by incubation and 52.4±2.4 mg C kg^–1 soil determined by extraction, accounting for 76% and 42% of the net flush of C measured by the chloroform fumigation. Microwave-stimulated net flushes of C were correlated closely (r ²=0.974 for incubation or 0.908 for extraction) with microbial biomass C measured by the chloroform fumigation. Little correlation was found with the total soil organic C (r ²=0.241 for incubation or for 0.166 extraction). Mean efficiency factors for incubation (K _MI) or extraction (K _ME) were used to calculate microbial biomass C from net flushes of C between microwaved and unmicrowaved soils. Values of K _MI and K _ME were not affected by soil pH, bulk density or clay contents. Extraction of microwaved soil by 0.5M K₂SO₄ proved to be a simple, fast, precise, reliable, and safe method to measure soil microbial biomass C. Received: 12 September 1997     

Critical sulphur concentration and sulphur requirement of microbial biomass in a glucose and cellulose-amended regosol

 The critical S concentration and S requirement of the soil microbial biomass of a granitic regosol was examined. S was applied at the rate of 0, 5, 10, 20, 30 and 50 μg S as MgSO₄·7H₂O, together with either 3000 μg glucose-C or 3333 μg cellulose-C, 400 μg N, and 200 μg P g ^–1 soil and 200 μg K g^–1 soil. Microbial biomass, inorganic SO₄ ^2–-S, and CO₂ emission were monitored over 30 days during incubation at 25  °C. Both glucose and cellulose decomposition rates responded positively to the S made available for microbial cell synthesis. The amounts of microbial biomass C and S increased with the level of applied S up to 10 μg S g^–1 soil and 30 μg S g^–1 soil in the glucose- and cellulose-amended soil, respectively, and then declined. Incorporated S was found to be concentrated within the microbial biomass or partially transformed into soil organic matter. The concentration of S in the microbial biomass was higher in the cellulose- (4.8–14.2 mg g^–1) than in the glucose-amended soil (3.7–10.9 mg g^–1). The microbial biomass C:S ratio was higher in the glucose- (46–142 : 1) than in the cellulose-amended soil (36–115 : 1). The critical S concentration in the microbial biomass (defined as that required to achieve 80% of the maximum synthesis of microbial biomass C) was estimated to be 5.1 mg g^–1 in the glucose- and 10.9 mg g^–1 in the cellulose-amended soil. The minimum requirement of SO₄ ^2–-S for microbial biomass formation was estimated to be 11 μg S g^–1 soil and 21 μg S g^–1 soil for glucose- and cellulose-amended soil, respectively. The highest levels of activity of the microbial biomass were observed at the SO₄ ^2–-S concentrations of 14 μg S g^–1 soil and 17 μg S g^–1 soil, for the glucose and cellulose amendments, respectively, and were approximately 31–54% higher during glucose than cellulose decomposition. Received: 20 October 1999     

Organic residues affect phosphorus availability and maize yields in a Nitisol of western Kenya

 The effects of organic residues and inorganic fertilizers on P availability and maize yield were compared in a Nitisol of western Kenya. Leaf biomass of Calliandra calothyrsus, Senna spectabilis, Croton megalocarpus, Lantana camara, Sesbania sesban, and Tithonia diversifolia were incorporated into the soil at 5 Mg ha^–1 for six consecutive seasons in 3 years and responses compared with those following the application of 120 kg N ha^–1, 0 kg P ha^–1 (0P); 120 kg N ha^–1, 10 kg P ha^–1; and 120 kg N ha^–1 25 kg P ha^–1 as urea and triple superphosphate (TSP); K was supplied in all treatments. Addition of Tithonia, Lantana and Croton increased soil resin-extractable P over that of fertilizer-amended soil throughout the first crop, but the amounts in the former treatments became similar to those for soils amended with inorganic fertilizers for subsequent crops. Addition of Sesbania, Calliandra and Senna had a similar effect on resin P as inorganic fertilizers. Total maize yields after six seasons were tripled by the application of Tithonia compared to 0P, and were higher than those of the Calliandra, Senna, Sesbania and Lantana treatments, and similar only to that of the Croton treatment. P recovered in the above-ground biomass and resin P, immediately after the implementation of the treatments, was higher in the Senna, Sesbania, Croton, Lantana and Tithonia (35–77%) treatments than in the inorganic fertilizer treatments (21–27%). The P content of organic residues, and the soluble C:total P ratio, were the main residue parameters predicting soil P availability and maize yield. All organic residues used in this study can replace inorganic fertilizers for the enhancement of P availability and maize production, while an additional benefit could be obtained from the use of Croton, Lantana and Tithonia. Received: 19 January 2000     

Effect of temperature on reduction of iron and production of carbon dioxide and methane in anoxic wetland rice soils

 Wetland rice soils from Italy (Pavia) and the Philippines (Bugallon, Luisiana, Maligaya) were incubated under anoxic conditions at 31 different temperatures ranging from 4.7  °C to 49.5  °C. Production of CO₂ was most intensive at the beginning of the incubation (0–4 days) and was predominantly coupled to the reduction of free Fe(III). The optimum temperature for these processes was between 32  °C and 41  °C. After 9–16 days, CO₂ production rates had decreased and the available Fe(III) had been completely reduced at the optimum temperatures. However, Fe(III) was still available at temperatures below and above the optimum. Maximum CH₄ production rates were observed after 4–16 days (except in soil from Maligaya) with temperature optima between 32  °C and 41  °C, similar to those for CO₂ production and Fe reduction. Since ongoing Fe reduction is known to suppress CH₄ production, the temperature range of optimum CH₄ production was restricted to those temperatures at which Fe(III) had already been depleted. Nevertheless, the temperature characteristics of both CO₂ and CH₄ production often exhibited two temperature optima at some time during the incubation, suggesting a complex pattern of adaptation of the methanogenic microbial community to temperature. When available Fe(III) was completely depleted by anoxic pre-incubation at 30  °C, CH₄ was produced at a constant rate (steady state conditions) which increased with increasing temperature. Steady state CH₄ production reached a first maximum at about 40  °C, but increased further up to at least 50  °C, suggesting the presence of thermophilic microorganisms whose activity was apparently masked when Fe had not been completely reduced. The apparent activation energy of CH₄ production at steady state ranged between 48 kJ mol^–1 and 65 kJ mol^–1. Received: 26 August 1999     

Microbial biomass and C mineralization in agricultural soils as affected by atrazine addition

This study examines the effects of atrazine on both microbial biomass C and C mineralization dynamics in two contrasting agricultural soils (organic C, texture, and atrazine application history) located at Galicia (NW Spain). Atrazine was added to soils, a Humic Cambisol (H) and a Gleyic Cambisol (G), at a recommended agronomic dose and C mineralization (CO₂ evolved), and microbial biomass measurements were made in non-treated and atrazine-treated samples at different time intervals during a 12-week aerobic incubation. The cumulative curves of CO₂–C evolved over time fit the simple first-order kinetic model [Ct = Co (1 − e ^−kt )], whose kinetic parameters were quantified. Differences in these parameters were observed between the two soils studied; the G soil, with a higher content in organic matter and microbial biomass C and lower atrazine application history, exhibited higher values of the total C mineralization and the potentially mineralizable labile C pool than those for the H soil. The addition of atrazine modified the kinetic parameters and increased notably the C mineralized; by the end of the incubation the cumulative CO₂–C values were 33–41% higher than those in the corresponding non-added soils. In contrast, a variable effect or even no effect was observed on the soil microbial biomass following atrazine addition. The data clearly showed that atrazine application at normal agricultural rates may have important implications in the C cycling of these two contrasting acid soils.     

Effects of long-term mineral fertilization on microbial biomass,microbial activity,and the presence of <Emphasis Type="Italic">r</Emphasis>- and <Emphasis Type="Italic">K</Emphasis>-strategists in soil

Long-term effects of mineral fertilization on microbial biomass C (MBC), basal respiration (R _B), substrate-induced respiration (R _S), β-glucosidase activity, and the r–K-growth strategy of soil microflora were investigated using a field trial on grassland established in 1969. The experimental plots were fertilized at three rates of mineral N (0, 80, and 160 kg ha⁻¹ year⁻¹) with 32 kg P ha⁻¹ year⁻¹ and 100 kg K ha⁻¹ year⁻¹. No fertilizer was applied on the control plots (C). The application of a mineral fertilizer led to lower values of the MBC and R _B, probably as a result of fast mineralization of available substrate after an input of the mineral fertilizer. The application of mineral N decreased the content of C extracted by 0.5 M K₂SO₄ (C _ex). A positive correlation was found between pH and the proportion of active microflora (R _S/MBC). The specific growth rate (μ) of soil heterotrophs was higher in the fertilized than in unfertilized soils, suggesting the stimulation of r-strategists, probably as the result of the presence of available P and rhizodepositions. The cessation of fertilization with 320 kg N ha⁻¹ year⁻¹ (NF) in 1989 also stimulated r-strategists compared to C soil, probably as the result of the higher content of available P in the NF soil than in the C soil.     

Nitrous oxide emissions from a fallow and wheat field as affected by increased soil temperatures

 In order to determine the effects of increased soil temperature resulting from global warming on microbiological reactions, a 21-month field experiment was carried out in the Bavarian tertiary hills. The major objective was to focus on N₂O releases as either a positive or negative feedback in response to global warming. The soils of a fallow field and a wheat field were heated 3  °C above ambient temperature and N₂O fluxes were measured weekly from June 1994 to March 1996. During the experimental period, measured temperature differences between the control plots and the heated plots were 2.9±0.3  °C at a depth of 0.01 m and 1.0–1.8  °C at a depth of 1 m. Soil moisture decreased with the elevated soil temperatures of the heated plots. The mean differences in soil moisture between the treatments were 6.4% (fallow field) and 5.2%_DW (wheat field dry weight, DW), respectively. Overall N₂O releases during the experimental period from the fallow field were 4.8 kg N₂O–N ha^–1 in the control plot against 5.0 kg N₂O–N ha^–1 in the heated plot, and releases from the wheat field were 8.0 N₂O–N ha^–1 in the control plot and 7.6 N₂O–N kg ha^–1 in the heated plot. However, on a seasonal basis, cumulated N₂O emissions differed between the plots. During the summer months (May–October), releases from the heated fallow plot were 3 times the rates from the control plot. In the winter months, N₂O releases increased in both the fallow and wheat fields and were related to the number of freezing and thawing cycles. Received: 1 December 1997     

Factors influencing nitrous oxide and methane emissions from minerotrophic fens in northeast Germany

 At two field sites representing northeastern German minerotrophic fens (Rhin-Havelluch, a shallow peat site; Gumnitz, a partially drained peat site) the influence of different factors (N fertilization, groundwater table, temperature) on N₂O and CH₄ emissions was investigated. The degraded fens were sources or sinks of the radiatively active trace gases investigated. The gas fluxes measured were much higher than those found in other terrestrical ecosystems such as forests. Lowering the groundwater table increased the release of N₂O and the oxidation of CH₄. High CH₄ emission rates occurred when the groundwater tables and soil temperatures were high (>12  °C). N fertilization stimulated the release of N₂O only when application rates were very high (480 kg N ha^–1). A moderate N supply (60 or 120 kg N ha^–1) hardly increased the release of N₂O in spite of high soluble soil NO₃ ^– contents. Received: 31 October 1997     

Nitrous oxide emission from Swedish forest soils in relation to liming and simulated increased N-deposition

Fluxes of N₂O were studied in a Norway spruce forest in the southwest of Sweden. Three differently treated catchments were compared: Limed (6 t dolomite ha^–1), Nitrex (additional N-deposition corresponding to 35 kg ha^–1 year^–1, in small doses) and Control (used as control site). The N-retention was still high (95%) after 2years of N-addition at the Nitrex site when the flux measurements were performed. Each catchment contained both well-drained and poorly drained soils (covered with Sphagnum sp.). The emissions of N₂O were in general low with both a high spatial and temporal variation for all three sites. The measured emissions were 25, 71 and 96 (gN₂O-N ha^–1 year^–1) for the well-drained Limed, Control and Nitrex sites, respectively. The average emissions of N₂O from the wet areas were significantly higher than the well-drained areas within the catchments. For the wet areas the measured emissions were larger: 90, 118 and 254 (g N₂O-N ha^–1 year^–1) for the Limed, Control and Nitrex sites, respectively. Comparison between treatments showed the wet Nitrex site to have a significantly higher emission than all other sites. The increased N-deposition at the Nitrex site increased the N₂O emissions by 0.2% of the added N for the well-drained soils and about 1% for the wet areas, compared with the control site. Since the wet areas represented only a small part of the forest, their larger emissions did not contribute significantly to the overall emission of the forest. Neither temperature nor water content of the soil was well correlated with the N₂O emissions. Soil gas samples showed that most of the N₂O was produced below a 0.3-m depth in the soil. Received: 27 September 1996     

Changes in soil microbial biomass, metabolic quotient, and organic matter turnover under Hieracium (H. pilosella L.)

 In New Zealand Hieracium is an opportunistic plant that invades high country sites more or less depleted of indigenous vegetation. To understand the invasive nature of this weed we assessed the changes in soil C, N and P, soil microbial biomass C, N and P contents, microbial C : N and C : P ratios, the metabolic quotient, and turnover of organic matter in soils beneath Hieracium and its adjacent herbfield resulting from the depletion of tussock vegetation. The amounts of soil organic C and total N were higher under Hieracium by 25 and 11%, respectively, compared to soil under herbfield. This change reflects an improvement in both the quantity and quality of organic matter input to mineral soil under Hieracium, with higher percentage organic C and a lower C : N ratio. The microbial biomass C, N and P contents were also higher under Hieracium. The amount of C respired during the 34-week incubation indicated differences in the nature of soil organic matter under Hieracium, the unvegetated "halo" zone surrounding Hieracium patches, and herbfield (depleted tussock grassland). Decomposition of organic matter in these zones showed that the Hieracium soil had the greatest rate of CO₂ respired, and the halo soil had the lowest. We relate the enhanced organic C turnover to the invasive nature of Hieracium. Net N mineralization was significantly lower from the Hieracium soil (57 mg N g^–1 soil N) than from herbfield and halo soils (74 and 71 mg N g^–1 soil N, respectively), confirming that the nature of organic N in Hieracium soil is different from adjoining halo and herbfield soils. It seems plausible that specific compounds such as polyphenols and lignins released by Hieracium are not only responsible for increased organic N, but also control the form and amount of N released during organic matter transformations. We conclude that the key to the success of Hieracium in the N-deficient South Island high country of New Zealand lies in its ability to control and sequester N supply through modifying the soil organic matter cycle. Received: 1 December 1998