Microbial response of an acid forest soil to experimental soil warming

 Effects of increased soil temperature on soil microbial biomass and dehydrogenase activity were examined on organic (O) horizon material in a low-elevation spruce-fir ecosystem. Soil temperature was maintained at 5  °C above ambient during the growing season in the experimental plots, and soil temperature, moisture, microbial biomass, and dehydrogenase activity were measured during the experiment. An incubation study was also conducted under three temperature regimes, 5, 15, and 25  °C, and under four moisture regimes of 20, 120, 220, and 320% to further evaluate these environmental factors on dehydrogenase activity and microbial biomass. Soil moisture content and microbial biomass controls were significantly lower (30% and 2 μg g^–1 soil, respectively) in the heated plots during the treatment period, suggesting that moisture content was important in controlling microbial biomass. In the incubation study, temperature appeared more important than moisture in controlling microbial biomass and dehydrogenase activity. Increasing temperature between 5  °C and 25  °C resulted in significant decreases in microbial biomass and dehydrogenase activity. Received: 7 August 1998     

Relationship between changes of soil microbial biomass content and imazamox and benfluralin degradation

The present research was carried out to determine the relationship between the soil microbial biomass content and the persistence of imazamox and benfluralin in three different soils, incubated in the laboratory under different conditions. The half-life values varied between 17.1 and 92.4 days for imazamox and 11.4 and 37.9 days for benfluralin depending on initial concentration, temperature, soil moisture and soil type. Significant decreases in microbial biomass-C content compared to untreated soil were observed initially, not exceeding 25.0% for imazamox and reaching 64.7% for benfluralin. The microbial biomass-C content then returned to initial values at varying times depending on incubation conditions. The relationship between herbicide persistence and microbial biomass-C content gave parabolic curves (P<0.001 in all cases) under all conditions tested. At the time of maximum microbial biomass decrease, the concentration of imazamox was generally about 50% of the initial dose (except for at 10°C for imazamox, when the biomass began to recover as early as the point when the pesticide concentration was at 60-65% of its initial dose). The final equation proposed could be useful to deduce the decrease in soil microbial biomass in relation to the herbicide level.     

Seasonal changes of microbial biomass carbon related to climatic factors in soils from karst areas of southwest China

 The seasonal responses of soil microbial biomass C to changes in atmospheric temperature, soil moisture and soluble organic C were studied in soils from the karst areas of southwest China. These soils are relatively weathered, leached and impoverished, and have a low input of plant residues. Over 1 year, an inverse relationship between soil microbial biomass C and atmospheric temperature was found. The highest microbial biomass C occurred in winter and the lowest in summer, and ranged from 231–723 μg g^–1 dry soil. Although there was no obvious relationship between microbial biomass C and soil moisture, a negative correlation existed between microbial biomass C and soluble organic C. In the ecosystem studied, the marked changes in soil microbial biomass C at above 20  °C were ascribed to fluctuations of soil moisture, which were controlled by climatic factors and geomorphic conditions. The patterns of soluble organic C turnover were similar to those of soluble carbohydrate C, both of which were controlled by soil drying-rewetting cycles. It was concluded that the lowest amounts of soil microbial biomass C, measured in the summer, resulted in increases in soluble organic C due to higher turnover rates of the former at warmer air temperatures. Thus, there was a marked seasonal change in soil microbial biomass C. Received: 1 November 1998     

Soil moisture and the rates of biodegradation of diallate and triallate

Degradation experiments were combined with biomass measurements and adsorption tests to determine how soil moisture content influences the rates of degradation of ⁴¹C-labelled diallate and triallate. In soils treated with 1 μg^?1 herbicide and incubated at constant temperature and moisture, degradation rates were regulated by two variables: the quantity of microbial biomass in the soil; and the quantity of herbicide dissolved in the soil solution. The quantity of biomass was influenced by soil water content and the duration of incubation. The amounts of herbicide in solution were determined by the amount of water present and the total quantity of herbicide in the soil. In all soil samples, the rates of degradation increased with increasing water content but decreased with prolonged incubation. The factors responsible for decrease with time were the loss of biomass during incubation and the decline in herbicide concentration in the soils as degradation proceeded.     

Effects of organic amendment and herbicide treatment on soil microbial biomass

 The interactive effects of vermi-compost from sewage sludge and either the sulfonylurea herbicide, rimsulfuron, or the imidazolinone herbicide, imazethapyr, on some soil biochemical and microbiological properties were investigated. The herbicides were applied at field and 10-fold field rates. Both herbicides exerted a detrimental effect on soil microbial biomass and its biochemical properties. Even though the effect of both herbicides on soil microbial biomass was not detectable at the field rate, some significant influences on acid and alkaline phosphatase were observed. The higher rate of herbicide application impaired the observed microbial parameters to a greater degree. The detrimental effects seemed to be reduced by organic amendments. Among the studied microbial characteristics, the specific respiration quotient was particularly reliable and sensitive in determining the influence of herbicides on the soil microbial biomass. In this paper a new synthetic index, specific hydrolytic activity (qFDA), for assessing microbial activity in reply to xenobiotic treatments is proposed. Received: 31 May 1999     

Impact of land-use change on nitrogen mineralization in subalpine grasslands in the Southern Alps

 A field study was conducted to investigate the effect of abandonment of management on net N mineralization (NNM) in subalpine meadows. NNM, soil microbial biomass N (SMBN), fungal biomass and physicochemical characteristics (total C, total N, dissolved organic carbon (DOC) and pH) were determined in surface (0–10 cm) soil from May to October 1997 in an intensively managed and an abandoned meadow at 1770 m a.s.l.. The cumulative NNM was lower in the abandoned area and ranged from 150 to 373 and from 25 to 85 μg N g^–1 soil in the intensively managed and the abandoned areas, respectively. The total organic C increased in the abandoned area, while total N showed no difference between abandoned and managed meadow. SMBN showed no difference between the investigated sites, whereas ergosterol, a measure of fungal biomass, increased significantly at the abandoned site. The cumulative NNM was negatively correlated with total organic C, C : N ratio, DOC and ergosterol content, and positively correlated with the NH₄ ⁺-N content of soil. The decrease in NNM at the abandoned site may be explained by the lower availability of N in substrates characterized by a high C : N ratio which, together with a decrease in pH in the litter layer, may have increased fungal biomass. Received: 8 January 1999     

Interaction of biochemical quality and particle size of crop residues and its effect on the microbial biomass and nitrogen dynamics following incorporation into soil

 Mineralization of N from organic materials added to soil depends on the quality of the substrate as a carbon, energy and nutrient source for the saprophytic microflora. Quality reflects a combination of biochemical and physical attributes. We investigated how biochemical composition interacts with particle size to affect the soil microflora and N dynamics following incorporation of crop residues into soil. Four fresh shoot and root crop residues were cut into coarse and fine particle sizes, and incorporated into sandy-loam soil which was incubated under controlled environment conditions for 6 months. In the case of the highest biochemical quality material, potato shoot (C/N ratio of 10 : 1), particle size had no effect on microbial respiration or net N mineralization. For lower biochemical quality Brussels sprout shoot (C/N ratio of 15 : 1), reducing particle size caused microbial respiration to peak earlier and increased net mineralization of N during the early stages of decomposition, but reduced net N mineralization at later stages. However, for the lowest biochemical quality residues, rye grass roots (C/N ratio of 38 : 1) and straw (C/N ratio of 91 : 1) reducing particle size caused microbial respiration to peak later and increased net immobilization of N. For Brussels sprout shoot, reducing particle size decreased the C content and the C/N ratio of residue-derived light fraction organic matter (LFOM) 2 months following incorporation. However C and N content of LFOM derived from the other materials was not affected by particle size. For materials of all qualities, particle size had little effect on biomass N. We conclude that the impact of particle size on soil microbial activities, and the protection of senescent microbial tissues from microbial attack, is dependant on the biochemical quality of the substrate. Received: 3 July 1998     

Response of the soil microbial biomass and nematode population to a wetting event in nitrogen-amended Negev desert plots

 Water and N availability are the major limiting factors of primary production in desert ecosystems, and the response of soil biota to these two factors is of great importance. We examined the immediate response of soil nematodes and the microbial biomass to a single pulse of water amendment in N-treated plots in the Israeli Negev desert. Plots were treated with 0, 50 and 100 kg NH₄NO₃ ha^–1 in December 1992, and at the end of the summer period (August 1993) the plots were exposed to a 15 mm water. Soil samples from the 0–10 cm layer were collected daily and analysed soil moisture, total soluble N, nematode populations and microbial biomass. Soil moisture increased to 8.5%, then gradually decreased to 2% during the 11 days of the study. Microbial biomass, soil respiration and metabolic quotient values did not exhibit any significant correlation with soil N levels. Free-living nematode population levels in the different plots were found to increase from a mean level of 45 500 to a mean level of 92 300 individuals m^–2. N treatment was found to affect the patterns of free-living nematode population dynamics. The results of this study demonstrated the importance of moisture availability levels and the ability to mobilize previous N inputs into available N which, occurring in pulses, can affect the microbial ecophysiological status, nematode population dynamics and the interrelationship between these two important components in the desert soil milieu. Received: 5 November 1998     

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     

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     

Soil characteristics,belowground diversity and rates of simazine mineralisation of a New Zealand Gley Soil in a chronosequence under horticultural use

The chemical, physical and biological conditions of a New Zealand Gley Soil was examined on matched sites under long-term permanent pasture or used to grow blackcurrants (Ribes nigrum) for 2, 8, 10 or 20 years. The chemical and physical conditions of topsoils (0–10 cm) were assessed by soil pH, Olsen P, total C, total N, mineralisable N, cation exchange, bulk density, porosity and moisture release characteristics. The biological conditions were assessed from the microbial biomass, soil respiration, catabolic evenness and numbers and diversity of the soil nematode populations. The ability of the soil populations to degrade the triazine herbicide simazine was tested. The particle size distribution confirmed all the sites were very well matched, within 2%, in terms of percentage clay, silt and sand contents, which were 36.5–40.5% clay and 59.5–62.5% silt. Compared with the soil under pasture, that under horticultural use for 2, 8, 10 and 20 years had lower total C and N, lower mineralisable N, lower cation exchange and lower porosity but higher bulk density and particle density. The differences were greater the longer the plots had been under blackcurrant production. Olsen P content was greatest (58 μg P cm⁻³) under the 20-year blackcurrant plots. Changes in biological characteristics were greater than in physical or chemical characteristics. Microbial biomass was 1.73 mg C cm⁻³ under pasture and decreased to 0.87 mg C cm⁻³ after 20 years of blackcurrants. Total nematode populations deceased from 3.89 million m⁻² under pasture to 0.36 million m⁻² after 2 years of blackcurrant production and to 108 000 m⁻² after 20 years. There were similar proportional decreases in bacterial-feeding, fungal-feeding, plant-feeding and omnivore nematodes; however, there was comparatively little change in nematode diversity (Shannon–Weiner) or in microbial catabolic diversity or soil respiration. Despite the decreased microbial biomass, the microbial community under blackcurrant production had enhanced capacity to degrade simazine, as compared with the pasture soil. That capacity to degrade simazine was similar in soils that had grown blackcurrants for 2, 8, 10 or 20 years. Yield of blackcurrants had been maintained in the longer-term sites, despite the marked changes in soil chemical, physical and biological conditions.     

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     

Relationships between microbial biomass and dissipation of 2,4-D and dicamba in soil

A study was conducted to evaluate relationships between microbial biomass and the dissipation of 2,4-D (2,4-dichlorophenoxy acetic acid) and dicamba (2-methoxy-3,6-dichlorobenzoic acid) in soil. We hypothesized that the size of the microbial biomass should be a strong predictor of the pesticide degradation capacity of a particular soil. Soils with a high microbial biomass should have relatively high levels of general microbial activity and should support a diversity of degradation pathways. In this study, we quantified the degradation of 2,4-D and dicamba in a range of soils with different concentrations of microbial biomass. The herbicides 2,4-D and dicamba were added to similar soils collected from five different land use types (home lawn, cornfield, upland hardwood forest, wetland forest, and aquifer material) and incubated for 80 days under laboratory conditions. Herbicide residue and microbial biomass (C and N) analyses were performed 5, 10, 20, 40, and 80 days following herbicide application. Microbial biomass-C and -N and soil organic matter content were positively correlated with dissipation of 2,4-D and dicamba. The results suggest that there are relationships between the size of the soil microbial biomass and the herbicide degradation capacity of an ecosystem. These relationships may be useful for developing approaches for evaluating and predicting the fate of pesticides in different ecosystems.     

Interactions between 14C-labelled atrazine and the soil microbial biomass in relation to herbicide degradation

A laboratory incubation experiment was set up to determine the effects of atrazine herbicide on the size and activity of the soil microbial biomass. This experiment was of a factorial design (0, 5, and 50 g g^–1 soil of non-labelled atrazine and 6.6×10³ Bq g^–1 soil of ¹⁴C-labelled atrazine) x (0, 20, and 100 g g^–1 soil of urea-N) x (pasture or arable soil with a previous history of atrazine application). Microbial biomass, measured by substrate-induced respiration and the fumigation-incubation method, basal respiration, incorporation of ¹⁴C into the microbial biomass, degradation of atrazine, and ¹⁴C remaining in soil were monitored over 81 days. The amount of microbial biomass was unaffected by atrazine although atrazine caused a significant enhancement of CO₂ release in the non-fumigated controls. Generally, the amounts of atrazine incorporated into the microbial biomass were negligible, indicating that microbial incorporation of C from atrazine is not an important mechanism of herbicide breakdown. Depending on the type of soil and the rate of atrazine application, 18–65% of atrazine was degraded by the end of the experiment. Although the pasture soil had twice the amount of microbial biomass as the arable soil, and the addition of urea approximately doubled the microbial biomass, this did not significantly enhance the degradation of atrazine. This suggests that degradation of atrazine is largely independent of the size of the microbial biomass and suggests that other factors (e.g., solubility, chemical hydrolysis) regulate atrazine breakdown. A separate experiment conducted to determine total amounts of ¹⁴C-labelled atrazine converted into CO₂ by pasture and arable soils showed that less than 25% of the added ¹⁴C-labelled atrazine was oxidised to ¹⁴CO₂ during a 15-week period. The rate of degradation was significantly greater in the arable soil at 24%, compared to 18% in the pasture soil. This indicates that soil microbes with previous exposure to atrazine can degrade the applied atrazine at a faster rate.     

Relationships between microbial biomass and dissipation of 2,4-D and dicamba in soil

A study was conducted to evaluate relationships between microbial biomass and the dissipation of 2,4-D (2,4-dichlorophenoxy acetic acid) and dicamba (2-methoxy-3,6-dichlorobenzoic acid) in soil. We hypothesized that the size of the microbial biomass should be a strong predictor of the pesticide degradation capacity of a particular soil. Soils with a high microbial biomass should have relatively high levels of general microbial activity and should support a diversity of degradation pathways. In this study, we quantified the degradation of 2,4-D and dicamba in a range of soils with different concentrations of microbial biomass. The herbicides 2,4-D and dicamba were added to similar soils collected from five different land use types (home lawn, cornfield, upland hardwood forest, wetland forest, and aquifer material) and incubated for 80 days under laboratory conditions. Herbicide residue and microbial biomass (C and N) analyses were performed 5, 10, 20, 40, and 80 days following herbicide application. Microbial biomass-C and -N and soil organic matter content were positively correlated with dissipation of 2,4-D and dicamba. The results suggest that there are relationships between the size of the soil microbial biomass and the herbicide degradation capacity of an ecosystem. These relationships may be useful for developing approaches for evaluating and predicting the fate of pesticides in different ecosystems.     

Isoproturon mineralization in an agricultural soil

The impact of soil moisture content and temperature on isoproturon (3-(4-isopropylphenyl)-1,1-dimethyl-urea [IPU]) mineralization activity was assessed on an agricultural soil regularly exposed to this herbicide. Mineralization of ¹⁴C-IPU was monitored on soil microcosms incubated at different temperatures (10°C, 20°C, 28°C) and soil moisture contents (9%, 12%, 15, 18%, 21%, 24%). An increase in temperature and/or soil moisture significantly enhanced the maximum rate and percentage of IPU mineralization while it decreased the lag time before mineralization. The maximum rate and percentage of IPU mineralization respectively ranged from 0.18% day⁻¹ and 9% for the lowest temperature and soil moisture content pair (10°C–9%) to 1.51% day⁻¹ and 27.1% for the highest pair (28°C–24%). Statistics revealed a cross interaction of temperature and soil moisture content on the maximum rate of IPU mineralization. The optimum conditions for IPU mineralization, estimated from the double Gaussian model, were 25.8°C and 24% soil moisture content. The influence of fluctuations in soil moisture content on IPU-mineralization was investigated by subjecting the soil microcosms to drought stress. When IPU was added at the end of the drought stress, it had no statistical effect on IPU mineralization. However, when it was added before the drought stress, two mineralization phases were observed: (1) one corresponding to the drought stress for which mineralization was low and (2) another one observed after restoration of soil moisture content characterized by higher mineralization rate. It can be concluded that climatic fluctuations affect the activity of IPU mineralizing microbial community, and may lead to an increase in IPU persistence.     

Influence of microbial activity and soil moisture on herbicide immobilization in soils

Mobility, extractability, and disappearance of the herbicides diuron, terbuthylazine, metolachlor, and pendimethalin were examined in incubation experiments with two topsoil samples of different natural microbial activity and after sterilization. Soil moisture was held constant at 10, 40, and 60 % WHC. In other variants, the soil water content was changed during the incubation. The four herbicides reveal a fairly different extent of microbial and chemical degradation and immobilization. The herbicide mobility – expressed by coefficients of partition between adsorbed and dissolved herbicide amounts – decreases at a lower rate and extent, when the microbial activity is low or the soil is sterile. With increasing initial soil moisture, also herbicide mobility and extractability increase; but in the course of time, abiotic immobilization occurs to a higher extent. When soil moisture changes during the incubation, formerly non‐extractable herbicide fractions (up to 40 % of the applied amounts) become extractable. Kinetics of herbicide immobilization follow an empirical sigmoidal function, which describes three periods of immobilization. The three‐period shape of the curve and its possible reasons are discussed for the data of the incubation experiments as well as for the results of a long‐term field trial with diuron.     

How increasing availabilities of carbon and nitrogen affect atrazine behaviour in soils

 The effect of increasing amounts of glucose and mineral N on the behaviour of atrazine was studied in two soils. One had been exposed to atrazine under field conditions (adapted soil), the other had not (non-adapted soil), resulting, respectively, in an accelerated degradation of atrazine in the adapted soil and in a slow degradation of the herbicide in the non-adapted soil. The dissipation of ¹⁴C-atrazine via degradation and formation of non-extractable "bound" residues was followed during laboratory incubations in soils supplemented or not with increasing amounts of glucose and mineral N. In both soils, glucose added at rates of up to 16 g C kg^–1 soil did not modify atrazine mineralization but increased the formation of bound residues; this was probably due to the retention of atrazine by the growing microbial biomass. Atrazine dealkylation was enhanced when a large amount of glucose was added. In both soils, the addition of the largest dose of mineral N (2.5 g N kg^–1 soil) decreased atrazine mineralization. The simultaneous addition of glucose and mineral N enhanced their effects. When the largest doses of mineral N and glucose were added, atrazine mineralization stopped in both soils, and the proportion of bound residues increased. Glucose and mineral N additions influenced atrazine mineralization to a greater extent in the adapted soil than in the non-adapted one, as revealed by ANOVA, although glucose addition had a greater effect than N. The competition for space and nutrients between atrazine-degrading microorganisms and the total heterotrophic microflora probably contributed to the decrease in atrazine mineralization. Received: 9 June 1998     

Relationship between soil neutral sugar composition and the amount of labile soil organic matter in Andisol treated with bark compost or leaf litter

 The effect of short-term bark compost (Ba) and leaf litter (Li) applications on the labile soil organic matter (SOM) status was investigated. The SOM status studied in this paper includes soil microbial biomass, soil available N, hot water extractable C (HwC) and N (HwN) and soil neutral sugar-C composition. The soil microbial biomass C (MBC) and N (MBN), soil available N, HwC and HwN increased upon application of Ba and Li. No quantitative relationship was observed between application of organic material and MBC, MBN or soil available N. A positive linear correlation was observed between MBN and HwC but not between MBN and soil available N. Among the various soil neutral sugar C, xylose C (Xyl) content in Ba plots showed a remarkable increase but mannose C (Man) did not differ among Fer (fertilizer), Ba or Li plots. Soil neutral sugar C had a positive linear correlation with soil available N, MBN and HwC. The proportion of MBN : TN is positively correlated with the Xyl/Man ratio. The increase in the proportion of MBN in SOM seems to occur with the increase of SOM derived from plant debris. Received: 20 October 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