Soil microbial biomass and nitrogen dynamics in a turfgrass chronosequence: A short-term response to turfgrass clipping addition

A mechanistic understanding of soil microbial biomass and N dynamics following turfgrass clipping addition is central to understanding turfgrass ecology. New leaves represent a strong sink for soil and fertilizer N, and when mowed, a significant addition to soil organic N. Understanding the mineralization dynamics of clipping N should help in developing strategies to minimize N losses via leaching and denitrification. We characterized soil microbial biomass and N mineralization and immobilization turnover in response to clipping addition in a turfgrass chronosequence (i.e. 3, 8, 25, and 97 yr old) and the adjacent native pines. Our objectives were (1) to evaluate the impacts of indigenous soil and microbial attributes associated with turf age and land use on the early phase decomposition of turfgrass clippings and (2) to estimate mineralization dynamics of turfgrass clippings and subsequent effects on N mineralization of indigenous soils. We conducted a 28-d laboratory incubation to determine short-term dynamics of soil microbial biomass, C decomposition, N mineralization and nitrification after soil incorporation of turfgrass clippings. Gross rates of N mineralization and immobilization were estimated with ¹⁵N using a numerical model, FLAUZ. Turfgrass clippings decomposed rapidly; decomposition and mineralization equivalent to 20-30% of clipping C and N, respectively, occurred during the incubation. Turfgrass age had little effect on decomposition and net N mineralization. However, the response of potential nitrification to clipping addition was age dependent. In young turfgrass systems having low rates, potential nitrification increased significantly with clipping addition. In contrast, old turfgrass systems having high initial rates of potential nitrification were unaffected by clipping addition. Isotope ¹⁵N modeling showed that gross N mineralization following clipping addition was not affected by turf age but differed between turfgrass and the adjacent native pines. The flush of mineralized N following clipping addition was derived predominantly from the clippings rather than soil organic N. Our data indicate that the response of soil microbial biomass and N mineralization and immobilization to clipping addition was essentially independent of indigenous soil and microbial attributes. Further, increases in microbial biomass and activity following clipping addition did not stimulate the mineralization of indigenous soil organic N.     

Seasonal variations of soil microbial biomass and activity in warm- and cool-season turfgrass systems

Plant growth can be an important factor regulating seasonal variations of soil microbial biomass and activity. We investigated soil microbial biomass, microbial respiration, net N mineralization, and soil enzyme activity in turfgrass systems of three cool-season species (tall fescue, Festuca arundinacea Schreb., Kentucky bluegrass, Poa pratensis L., and creeping bentgrass, Agrostis palustris L.) and three warm-season species (centipedegrass, Eremochloa ophiuroides (Munro.) Hack, zoysiagrass, Zoysia japonica Steud, and bermudagrass, Cynodon dactylon (L.) Pers.). Microbial biomass and respiration were higher in warm- than the cool-season turfgrass systems, but net N mineralization was generally lower in warm-season turfgrass systems. Soil microbial biomass C and N varied seasonally, being lower in September and higher in May and December, independent of turfgrass physiological types. Seasonal variations in microbial respiration, net N mineralization, and cellulase activity were also similar between warm- and cool-season turfgrass systems. The lower microbial biomass and activity in September were associated with lower soil available N, possibly caused by turfgrass competition for this resource. Microbial biomass and activity (i.e., microbial respiration and net N mineralization determined in a laboratory incubation experiment) increased in soil samples collected during late fall and winter when turfgrasses grew slowly and their competition for soil N was weak. These results suggest that N availability rather than climate is the primary determinant of seasonal dynamics of soil microbial biomass and activity in turfgrass systems, located in the humid and warm region.     

Soil microbial biomass, activity and potential nitrogen mineralization in a pasture: Impact of stock camping activity

Grazing animals recycle a large fraction of ingested C and N within a pasture ecosystem, but the redistribution of C and N via animal excreta is often heterogeneous, being highest in stock camping areas, i.e., near shade and watering sources. This non-uniform distribution of animal excreta may modify soil physical and chemical attributes, and likely affect microbial community eco-physiology and soil N cycling. We determined microbial population size, activity, N mineralization, and nitrification in areas of a pasture with different intensity of animal excretal deposits (i.e., stock camping, open grazing and non-grazing areas). The pasture was cropped with coastal bermudagrass (Cynodon dactylon L.) and subjected to grazing by cattle for 4 y. Soil microbial biomass, activity and N transformations were significantly higher at 0-5 cm than at 5-15 cm soil depth, and the impacts of heterogeneous distribution of animal excreta were more pronounced in the uppermost soil layer. Microbial biomass, activity and potential net N mineralization were greater in stock camping areas and were significantly correlated (r²≈0.50, P<0.05) with the associated changes in total soil C and N. However, gross N mineralization and nitrification potential tended to be lower in stock camping areas than in the open grazing areas. The lower gross N mineralization, combined with greater net N mineralization in stock camping areas, implied that microbial N immobilization was lower in those areas than in the other areas. This negative association between microbial N immobilization and soil C is inconsistent with a bulk of publications showing that microbial N immobilization was positively related to the amount of soil C. We hypothesized that the negative correlation was due to microbial direct utilization of soluble organic N and/or changes in microbial community composition towards active fungi dominance in stock camping areas.     

Soil microbial biomass and activity in organic tomato farming systems: Effects of organic inputs and straw mulching

Organic farming is rapidly expanding worldwide. Plant growth in organic systems greatly depends on the functions performed by soil microbes, particularly in nutrient supply. However, the linkages between soil microbes and nutrient availability in organically managed soils are not well understood. We conducted a long-term field experiment to examine microbial biomass and activity, and nutrient availability under four management regimes with different organic inputs. The experiment was initiated in 1997 by employing different practices of organic farming in a coastal sandy soil in Clinton, NC, USA. Organic practices were designed by applying organic substrates with different C and N availability, either in the presence or absence of wheat-straw mulch. The organic substrates used included composted cotton gin trash (CGT), animal manure (AM) and rye/vetch green manure (RV). A commercial synthetic fertilizer (SF) was used as a conventional control. Results obtained in both 2001 and 2002 showed that microbial biomass and microbial activity were generally higher in organically than conventionally managed soils with CGT being most effective. The CGT additions increased soil microbial biomass C and activity by 103-151% and 88-170% over a period of two years, respectively, leading to a 182-285% increase in potentially mineralizable N, compared to the SF control. Straw mulching further enhanced microbial biomass, activity, and potential N availability by 42, 64, and 30%, respectively, relative to non-mulched soils, likely via improving C and water availability for soil microbes. The findings that microbial properties and N availability for plants differed under different organic input regimes suggest the need for effective residue managements in organic tomato farming systems.     

Soil microbial biomass and nitrogen transformations among five tree species of the Catskill Mountains, New York, USA

We measured soil microbial biomass nitrogen (MBN), microbial uptake of ¹⁵N, potential net mineralization and net nitrification in the laboratory to determine the influence of tree species on nitrogen (N) transformations in soils of the Catskills Mountains, New York, USA. Organic horizon soils were taken from single species plots of beech (Fagus grandifolia), hemlock (Tsuga canadensis), red oak (Quercus rubra), sugar maple (Acer saccharum) and yellow birch (Betula alleghaniensis). ¹⁵NH₄Cl was added to the soils and N pools were sampled at 1, 3, 10 and 28 days to examine microbial uptake of ¹⁵N over time. Soil MBN was about 60% lower in red oak and sugar maple soils than in the other three species. Soil pools of NO₃⁻ and rates of net nitrification were significantly greater in soils associated with sugar maple than hemlock, red oak and yellow birch. With the exception of sugar maple soils, microbial recovery of ¹⁵N was significantly greater after 10 and 28 days compared to 60 min and 1 day following ¹⁵N tracer addition. Microbial ¹⁵N recovery declined significantly within sugar maple stands within the first 3 days of incubation. Soil carbon to nitrogen ratio (C:N) was lowest in sugar maple soils and highest in red oak soils. However, correlations between soil C:N and MBN or rates of net mineralization and nitrification were not significant. Soil moisture could account for 22% of the variation in MBN and 36% of the variation in net mineralization. Soil microbial transformations of N vary among tree species stands and may have consequences for forest N retention and loss.     

Effect of bamboo harvest on dynamics of nutrient pools,N mineralization,and microbial biomass in soil

The effect of harvesting bamboo savanna on the dynamics of soil nutrient pools, N mineralization, and microbial biomass was examined. In the unharvested bamboo site NO _inf3 ^sup- -N in soil ranged from 0.37 to 3.11 mg kg^-1 soil and in the harvested site from 0.43 to 3.67 mg kg^-1. NaHCO₃-extractable inorganic P ranged from 0.55 to 3.58 mg kg^-1 in the unharvested site and from 1.01 to 4.22 mg kg^-1 in the harvested site. Over two annual cycles, the N mineralization range in the unharvested and harvested sites was 0–19.28 and 0–24.0 mg kg^-1 soil month^-1, respectively. The microbial C, N, and P ranges were 278–587, 28–64, and 12–26 mg kg^-1 soil, respectively, with the harvested site exhibiting higher values. Bamboo harvesting depleted soil organic C by 13% and total N by 20%. Harvesting increased N mineralization, resulting in 10 kg ha^-1 additional mineral N in the first 1st year and 5 kg ha^-1 in the 2nd year following the harvest. Microbial biomass C, N and P increased respectively by 10, 18, and 5% as a result of bamboo harvesting.     

Responses of microbial biomass and respiration of soil to topography,burning, and nitrogen fertilization in a temperate steppe

Temporal dynamics of microbial biomass and respiration of soil and their responses to topography, burning, N fertilization, and their interactions were determined in a temperate steppe in northern China. Soil microbial indices showed strong temporal variability over the growing season. Soil microbial biomass C (MBC) and N (MBN) were 14.8 and 11.5% greater in the lower than upper slope, respectively. However, the percentage of organic C present as MBC and the percentage of total N present as MBN were 16.9 and 26.2% higher in the upper than lower slope, respectively. Neither microbial respiration (MR) nor metabolic quotient (qCO₂) was affected by topography. Both MBC and MBN were increased by burning, on average, by 29.8 and 14.2% over the growing season, and MR and qCO₂ tended to reduce depending on the sampling date, especially in August. Burning stimulated the percentage of organic C present as MBC and the percentage of total N present as MBN in the upper slope, but did not change these two parameters in the lower slope. No effects of N fertilization on soil microbial indices were observed in the first growing season after the treatment. Further research is needed to study the long-term relationships between changes in soil microbial diversity and activity and plant community in response to burning and N fertilization.     

Effect of glucose amendment on microbial biomass,spelling fertilizer 15N-recovery and distribution in a barley-soil-system

Summary One way to conserve fertilizer N in the plant-soil system is to immobilize it at the time of application by adding a readily available C source and to rely on the microorganisms to remineralize it to meet crop N demand during the season. The present study was conducted to determine the effects of microbial activity due to glucose amendment at the time of fertilization and planting on the distribution of fertilizer ¹⁵N at harvest among various N pools. Glucose C (150 g m^-2) was added to soil at Ellerslie (Black Chernozem) in central Alberta at the time of seeding and fertilization with urea-¹⁵N (7.5 g m^-2). Barley shoot mass, root mass, and root N at harvest in the non-glucose treatment were 1.8-fold, 1.9-fold, and 2.2-fold greater, respectively, than in the glucose treatment. The recovery of ¹⁵N in the soil-plant system was greater in the glucose (82%) than the non-glucose treatment (50%). Likewise, the recovery of ¹⁵N in soil was greater in the glucose treatment (72%) than the non-glucose treatment (22%). In both treatments most soil ¹⁵N remaining at the time of harvest was present as non-microbial organic ¹⁵N, but recovery of ¹⁵N in this pool was 3.4-fold greater in glucose-treated than in non-glucose-treated soil. The microbial response to the glucose addition effectively conserved fertilizer N in the active N phase; however, significant remineralization did not occur to meet plant N demands. Microbial transformations in the soil resulted in a constant ratio of non-microbial organic N formed per unit of microbial N formed and this ratio was not affected by the C amendments.     

Seasonal fluctuation in microbial biomass and activity along a natural nitrogen gradient in a drained peatland

The effects of peat total N on the dissolved N and C concentrations and microbial biomass and activity and their range of seasonal fluctuation were studied in a drained peatland forest in Finland. Seasonal fluctuations in the concentrations of extractable dissolved organic (DON) and inorganic nitrogen (DIN) compounds and extractable dissolved organic carbon (DOC), microbial C and N, ergosterol, net and gross N mineralisation rates were investigated during two growing seasons along a natural peat N gradient in a drained peatland. Significant seasonal fluctuations in NH₄⁺ and DOC concentrations, microbial C and N, but not in ergosterol or microbial C-to-N ratios in the peat, were observed during the 1999 and 2000 growing seasons. The peat total N concentration affected extractable DON and DOC, but not DIN concentrations in the peat. A negative correlation was found between total N concentration in peat and microbial N and C, and a positive correlation between total N and ergosterol, in peat with N concentrations of up to 2%. Gross mineralisation rates did not show any correlation, whereas net mineralisation rates showed a significant positive correlation with the total N concentration of the peat in both 1999 and 2000.     

Soil microbial biomass and activities in a Japanese Andisol as affected by controlled release and application depth of urea

This experiment was conducted in maize field plots to study the effects of controlled release and application depth of urea on soil microbial biomass and activities at two depths of surface soil of a Japanese Andisol from June to September, 2001. Three N amendment treatments and a Control were included in this experiment: deep application (8 cm) of controlled release urea; deep application (8 cm) of conventional urea; surface application of conventional urea; Control, without N application. Prior to this experiment, the field plots received the same N fertilizer treatments for two consecutive years under maize/barley rotation. Soil microbial biomass, dehydrogenase and nitrification activities exhibited great vertical and temporal variations during the maize growth season, and the microbial biomass was significantly correlated to soil water-filled pore space (p<0.01). N fertilization did not significantly affect the microbial biomass, but greatly increased the dehydrogenase and nitrification activities. The increase in the microbial activities following N fertilization was not attributed to the increase in microbial biomass but to the increase in intrinsic microbial activities. Controlled release urea was found to continuously affect the dehydrogenase activity over a shorter distance, while conventional urea could greatly increase the enzyme activity for a shorter period of time. Both controlled release and deep application of urea had potentials to reduce the nitrification activity and suggested that the nitrate production might be decreased in 0–10 cm surface soil. Deep application of urea increased aboveground N uptake by maize and then the recovery rate of N fertilizer, whereas controlled release of urea greatly increased grain yield and N uptake by grain.     

土壤微生物生物氮与植物氮吸收的关系

The contents of the soil microbial biomass nitrogen (SMBN) in the soils sampled from the Loess Plateau of China were determined using chloroform fumigation aerobic incubation method (CFAIM),chloroform fumigation anaerobic incubation method (CFANIM) and chloroform fumigation-extraction method (CFEM). The N taken up by ryegrass on the soils was determined after a galsshouse pot experiment. The flushes of nitrogen (FN) of the soils obtained by the CFAIM and CFANIM were higher than that by the CFEM, and there were significantly positive correlations between the FN obtained by the 3 methods. The N extracted from the fumigated soils by the CFAIM,CFANIM and CFEM were significantly positively correlated with the N uptake by ryegrass. The FN obtained by the 3 methods was also closely positively correlated with the N uptake by ryegrass. The FN obtained by the 3 methods was also closely positively correlated with the plant N uptake. The contributions of the SMBN and mineral N and mineralized N during the incubation period to plant N uptake were evaluated with the multiple regression method. The results showed that the N contained in the soil microbial biomass might play a noticeable role in the N supply of the soils to the plant.     

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     

Earthworms increase soil microbial biomass carrying capacity and nitrogen retention in northern hardwood forests

Earthworms have been shown to produce contrasting effects on soil carbon (C) and nitrogen (N) pools and dynamics. We measured soil C and N pools and processes and traced the flow of ¹³C and ¹⁵N from sugar maple (Acer saccharum Marsh.) litter into soil microbial biomass and respirable C and mineralizable and inorganic N pools in mature northern hardwood forest plots with variable earthworm communities. Previous studies have shown that plots dominated by either Lumbricus rubellus or Lumbricus terrestris have markedly lower total soil C than uncolonized plots. Here we show that total soil N pools in earthworm colonized plots were reduced much less than C, but significantly so in plots dominated by contain L. rubellus. Pools of microbial biomass C and N were higher in earthworm-colonized (especially those dominated by L. rubellus) plots and more ¹³C and ¹⁵N were recovered in microbial biomass and less was recovered in mineralizable and inorganic N pools in these plots. These plots also had lower rates of potential net N mineralization and nitrification than uncolonized reference plots. These results suggest that earthworm stimulation of microbial biomass and activity underlie depletion of soil C and retention and maintenance of soil N pools, at least in northern hardwood forests. Earthworms increase the carrying capacity of soil for microbial biomass and facilitate the flow of N from litter into stable soil organic matter. However, declines in soil C and C:N ratio may increase the potential for hydrologic and gaseous losses in earthworm-colonized sites under changing environmental conditions.     

Effect of novaluron on microbial biomass,respiration, and fluorescein diacetate-hydrolyzing activity in tropical soils

The aim of this study was to assess the potential harmful effects of novaluron on soil microbiological parameters in clay loam alluvial soil (Typic udifluvent) and coastal saline soil (Typic endoaquept) under controlled laboratory tests. The applications of novaluron were made at or above the recommended rates, which includes field rate (FR), two times (2FR), and ten times (10FR) the FR. The laboratory incubation study was carried out at 60% of maximum water holding capacity of soils and at 30°C. Novaluron application rate even up to 10FR resulted in a short-lived and transitory toxic effect on soil microbial biomass C and fluorescein diacetate-hydrolyzing activity. Microbial metabolic quotient changed but for a short period. It can be concluded that novaluron had a transient and negligible harmful effect on the soil microbiological parameters studied at higher rates than those usually used in the field.     

Ratios between estimates of microbial biomass content and microbial activity in soils

The content levels and activities of the microbiota were estimated in topsoils and in one soil profile at agricultural and forest sites of the Bornhöved Lake district in northern Germany. Discrepancies between data achieved by fumigation-extraction (FE) and substrate-induced respiration (SIR), both used for the quantification of microbial biomass, were attributed to the composition of the microbial populations in the soils. In the topsoils, the active, glucose-responsive (SIR) versus the total, chloroform-sensitive microbial (FE) biomass decreased in the order; field maize monoculture (field-MM)>field crop rotation (field-CR) and dry grassland>beech forest. This ratio decreased within the soil profile of the beech forest from the litter horizon down to the topsoil. Differences between microbial biomass and activities suggested varying biomass-specific transformation intensities in the soils. The metabolic quotient (qCO₂), defined as the respiration rate per unit of biomass, indicates the efficiency in acquiring organic C and the intensity of C mineralization, while biomass-specific arginine-ammonification (arginine-ammonification rate related to microbial biomass content) seems to be dependent on N availability. The qCO₂, calculated on the basis of the total microbial biomass, decreased for the topsoils in the same order as did the ratio between the active, glucose-responsive microbial biomass to the total, chloroform-sensitive microbial biomass, in contrast to qCO₂ values based on the glucose-responsive microbial biomass, which did not. There was no difference between the levels of biomass-specific arginine-ammonification in topsoils of the fertilized field-CR, fertilized field-MM, fertilized dry grassland and eutric alder forest, but levels were lower in the beech forest, dystric alder forest, and unfertilized wet grassland topsoils. Ratios between values of different microbiological features are suggested to be more useful than microbiological features related to soil weight when evaluating microbial populations and microbially mediated processes in soils.     

Soil microbial biomass and activity under a potato crop fertilised with N with and without C

Summary A range of soil microbiological parameters were measured at intervals throughout the growing season of a potato crop. Treatments applied to the soil at sowing were zero N fertilisation of N fertilisation at 120 kg N ha^–1, either alone or supplemented with straw or sucrose at 1200 kg C ha^–1. C and N flushes determined by fumigation-incubation and fumigation-extraction, and substrate-induced respiration, were measured as indicators of microbial biomass. Microbial activity was measured as respiration (CO₂ production) and dehydrogenase activity (formazan production). The greatest effects were obtained from the addition of N plus sucrose. Both biomass size and activity were significantly stimulated for up to 25 days after incorporation, with the magnitude of the effects consistently diminishing over time. By 125 days after planting, there was no detectable legacy from any of the treatmentson any of the biomass parameters that were measured, and all values had reverted to those prevalent at planting. There was no consistent effect from adding N, either alone or supplemented with straw, on any of the biomass parameters. There was no evidence for crop-induced stimulation of the biomass. The experiment demonstrates that biomass is only influenced where the quantity, quality, and rate of incorporation of C into the soil is appropriate, in this case, only by adding C as a pulse of sucrose.     

Microbial biomass and C and N transformations in forest floors under European beech, sessile oak, Norway spruce and Douglas-fir at four temperate forest sites

The purpose of this research was to compare soil chemistry, microbially mediated carbon (C) and nitrogen (N) transformations and microbial biomass in forest floors under European beech (Fagus sylvatica L.), sessile oak (Quercus petraea (Mattuschka) Lieblein), Norway spruce (Picea abies (L.) Karst) and Douglas-fir (Pseudotsuga menziesii (Mirbel) Franco) at four study sites. We measured soil chemical characteristics, net N mineralization, potential and relative nitrification, basal respiration, microbial and metabolic quotient and microbial biomass C and N under monoculture stands at all sites (one mixed stand). Tree species affected soil chemistry, microbial activities and biomass, but these effects varied between sites. Our results indicated that the effect of tree species on net N mineralization was likely to be mediated through their effect on soil microbial biomass, reflecting their influence on organic matter content and carbon availability. Differences in potential nitrification and relative nitrification might be related to the presence of ground vegetation through its influence on soil NH₄ and labile C availability. Our findings highlight the need to study the effects of tree species on microbial activities at several sites to elucidate complex N cycle interactions between tree species, ground vegetation, soil characteristics and microbial processes.     

The influence of two agricultural biostimulants on nitrogen transformations, microbial activity, and plant growth in soil microcosms

The influence of two experimental soil treatments, Z93 and W91, on nitrogen transformations, microbial activity and plant growth was investigated in soil microcosms. These compounds are commercially marketed fermentation products (Agspectrum) that are sold to be added to field soils in small amounts to promote nitrogen and other nutrient uptake by crops in USA. In laboratory microcosm experiments, soils were amended with finely ground alfalfa-leaves or wheat straw, or left unamended, in an attempt to alter patterns of soil nitrogen mineralization and immobilization. Soils were treated in the microcosms with Z93 and W91 at rates equivalent to the recommended field application rates, that range from 0.2 to 1.1 l ha⁻¹, (0.005-0.03 μl g⁻¹ soil). We measured their effects on soil microbial activity (substrate-induced respiration (SIR), dehydrogenase activity (DHA) and acid phosphatase activity (PHOS)), soil nitrogen pools (microbial biomass N, mineral N, dissolved organic N), and transformations (net N mineralization and nitrification, ¹⁵N dilution of the mineral N pool, and accumulation of mineral N on ion-exchange resins), and on wheat plant germination and growth (shoot and root biomass, shoot length, N uptake and ¹⁵N enrichment of shoot tissues), for up to 56 days after treatment. To follow the movement of nitrogen from inorganic fertilizer into plant biomass we used a ¹⁵N isotopic tracer. Most of the soil and plant responses to treatment with Z93 or W91 differed according to the type of organic amendment that was used. Soil treatment with either Z93 or W91 influenced phosphatase activity strongly but did not have much effect on SIR or DHA. Both chemicals altered the rates of decomposition and mineralization of organic materials in the soil, which was evidenced by significant increases in the rates of the decomposition of buried wheat straw, and by the acceleration of net, rates of N mineralization, relative to those of the controls. Soil nitrate availability increased at the end of the experiment in response to both chemical treatments. In alfalfa-amended soils, the final plant biomass was decreased significantly by treatment with W91. Increased plant growth and N-use efficiency in straw-amended soil, resulting from treatments with Z93 or W91, was linked to increased rates of N mineralization from indigenous soil organic materials. This supports the marketing of these compounds as promoters of N uptake at these low dosage inputs.     

Effects of fertilizer application and fire regime on soil microbial biomass carbon and nitrogen,and nitrogen mineralization in an Australian subalpine eucalypt forest

The effects of a range of fertilizer applications and of repeated low-intensity prescribed fires on microbial biomass C and N, and in situ N mineralization were studied in an acid soil under subalpine Eucalyptus pauciflora forest near Canberra, Australia. Fertilizer treatments (N, P, N+P, line + P, sucrose + P), and P in particular, tended to lower biomass N. The fertilizer effects were greatest in spring and smaller in summer and late actumn. Low-intensity prescribed fire lowered biomass N at a soil depth of 0–5 cm with the effect being greater in the most frequently burnt soils. No interactions between fire treatments, season, and depth were significant. Only the lime + P and N+P treatments significantly affected soil microbial biomass C contents. The N+P treatment increased biomass C only at 0–2.5 cm in depth, but the soil depth of entire 0–10 cm had much higher (>doubled) biomass C values in the line + P treatment. Frequent (two or three times a year) burning reduced microbial boomass C, but the reverse was true in soils under forest burn at intervals of 7 years. Soil N mineralization was increased by the addition of N and P (alone or in combination), line + P, and sucrose + P to the soil. The same was true for the ratio of N mineralization to biomass N. Soil N mineralization was retarded by repeated fire treatments, especially the more frequent fire treatment where rates were only about half those measured in unburnt soils. There was no relationship between microbial biomass N (kg N ha^-1) and the field rates of soil N mineralization (kg N ha^-1 month^-1). The results suggest that although soil microbial biomass N represents a distinct pool of N, it is not a useful measure of N turnover.     

Impact of land-use types on soil nitrogen net mineralization in the sandstorm and water source area of Beijing,China

Changes of land-use type (LUT) can affect soil nutrient pools and cycling processes that relate long-term sustainability of ecosystem, and can also affect atmospheric CO₂ concentrations and global warming through soil respiration. We conducted a comparative study to determine NH₄⁺ and NO₃⁻ concentrations in soil profiles (0–200 cm) and examined the net nitrogen (N) mineralization and net nitrification in soil surface (0–20 cm) of adjacent naturally regenerated secondary forests (NSF), man-made forests (MMF), grasslands and cropland soils from the windy arid and semi-arid Hebei plateau, the sandstorm and water source area of Beijing, China. Cropland and grassland soils showed significantly higher inorganic N concentrations than forest soils. NO₃⁻-N accounted for 50–90% of inorganic N in cropland and grassland soils, while NH₄⁺-N was the main form of inorganic N in NSF and MMF soils. Average net N-mineralization rates (mg kg⁻¹ d⁻¹) were much higher in native ecosystems (1.51 for NSF soils and 1.24 for grassland soils) than in human disturbed LUT (0.15 for cropland soils and 0.85 for MMF soils). Net ammonification was low in all the LUT while net nitrification was the major process of net N mineralization. For more insight in urea transformation, the increase in NH₄⁺ and, NO₃⁻ concentrations as well as C mineralization after urea addition was analyzed on whole soils. Urea application stimulated the net soil C mineralization and urea transformation pattern was consistent with net soil N mineralization, except that the rate was slightly slower. Land-use conversion from NSF to MMF, or from grassland to cropland decreased soil net N mineralization, but increased net nitrification after 40 years or 70 years, respectively. The observed higher rates of net nitrification suggested that land-use conversions in the Hebei plateau might lead to N losses in the form of nitrate.