Differential and successive effects of residue quality and soil mineral N on water-stable aggregation during crop residue decomposition

Residue quality has been shown to influence soil water-stable aggregation (WSA) during crop residue decomposition, but there is still little information about its interactive effect with soil mineral N availability. The aim of this study was to determine the effect of soil mineral N on WSA during the decomposition of two high-C/N crop residues (wheat straw with C/N = 125.6 and miscanthus straw with C/N = 311.3). The two crop residues were combined with three mineral N addition rates (0, 60, and 120 mg N kg⁻¹ dry soil). Respiration, soil mineral N content, and WSA (expressed as mean-weight diameter, MWD) were measured on several dates during a 56-d incubation. The effect of decomposing crop residues on WSA followed two phases. (i) Between 0 and 7 d, the increase in WSA was related to intrinsic residue quality with higher decomposability of the wheat straw resulting in higher WSA. (ii) Thereafter, and until the end of the experiment, mineral N addition rates had a predominant but negative influence on WSA. In this second phase, the average MWD of residue-treated soils was 0.92, 0.55, and 0.44 mm for the 0, 60 and 120 mg N kg⁻¹ dry soil addition rates, respectively. Mineral N addition which did result in higher crop residue decomposition did not lead to higher WSA. WSA during crop residue decomposition is therefore not simply positively related to the induced microbial activity, and changes in microbial community composition with differential effects on WSA must be involved. The impact of high-C/N crop residues inputs on WSA, initially assumed to be low, could actually be strong and long-lasting in situations with low soil mineral N content.     

Changes during winter in water‐stable aggregation due to crop residue quality

There is a need to develop practices that contribute to increased water‐stable aggregation (WSA) during winter in a humid temperate climate when soil is particularly prone to water erosion. Our objectives were to determine the effects of crop residue quality on WSA during winter and to relate these effects to biochemical indicators of fungal and bacterial biomass. Three graminae crop residues were selected for their different C/N ratios and biochemical characteristics (green oat residues, C/N = 18.8; wheat straw, C/N = 125.6; and mature miscanthus residues, C/N = 311.3). In October 2009, crop residues were added with an equivalent amount of C in the 0–10 cm layer to a Luvisol in north‐west France. WSA, expressed as mean weight diameter (MWD), amino sugar, soil mineral N and water contents were measured at regular intervals during 5 months. Aggregate MWD of the control soil decreased rapidly and remained low until the last sampling date in March which illustrates the structural vulnerability of bare soils in winter in this pedo‐climatic area. The incorporation of all three crop residues had significant positive impacts on aggregate MWD. Despite widely different C/N ratios, the maximum MWD under each treatment was similar (three times greater than the control soil). Maximum MWD occurred at times that clearly depended on residue quality. Maximum values occurred early for green oat (29 day), but were delayed to 50 day for wheat straw and to 154 day for miscanthus. Results from correlation analysis suggest that variations in WSA were partly mediated by microbial agents with a dominant effect of bacteria for green oat and a combined role of fungal and bacterial biomass for wheat straw. We suggest that the maximum MWD associated with the miscanthus late in the experiment is related to changes in the composition of the fungal community. Overall, our study shows that autumn application of crop residues increases WSA during winter with its effect being microbially mediated and determined by residue quality.     

Mechanisms of soil N dynamics following long-term application of organic fertilizers to subtropical rain-fed purple soil in China

In this study, a ¹⁵N tracing incubation experiment and an in situ monitoring study were combined to investigate the effects of different N fertilizer regimes on the mechanisms of soil N dynamics from a long-term repeated N application experiment. The field study was initiated in 2003 under a wheat-maize rotation system in the subtropical rain-fed purple soil region of China. The experiment included six fertilization treatments applied on an equivalent N basis (280 kg N ha⁻¹), except for the residue only treatment which received 112 kg N ha⁻¹: (1) UC, unfertilized control; (2) NPK, mineral fertilizer NPK; (3) OM, pig manure; (4) OM-NPK, pig manure (40% of applied N) with mineral NPK (60% of applied N); (5) RSD, crop straw; (6) RSD-NPK, crop straw (40% of applied N) with mineral NPK (60% of applied N). The results showed that long-term repeated applications of mineral or organic N fertilizer significantly stimulated soil gross N mineralization rates, which was associated with enhanced soil C and N contents following the application of N fertilizer. The crop N offtake and yield were positively correlated with gross mineralization. Gross autotrophic nitrification rates were enhanced by approximately 2.5-fold in the NPK, OM, OM-NPK, and RSD-NPK treatments, and to a lesser extent by RSD application, compared to the UC. A significant positive relationship between gross nitrification rates and cumulative N loss via interflow and runoff indicated that the mechanisms responsible for increasing N loss following long-term applications of N fertilizer were governed by the nitrification dynamics. Organic fertilizers stimulated gross ammonium (NH₄⁺) immobilization rates and caused a strong competition with nitrifiers for NH₄⁺, thus preventing a build-up of nitrate (NO₃⁻). Overall, in this study, we found that partial or complete substitution of NPK fertilizers with organic fertilizers can reduce N losses and maintain high crop production, except for the treatment involving application of RSD alone. Therefore, based on the N transformation dynamics observed in this study, organic fertilizers in combination with mineral fertilizer applications (i.e. OM, OM-NPK, and RSD-NPK treatments) are recommended for crop production in the subtropical rain-fed purple soils in China.     

双季稻田添加脲酶抑制剂NBPT氮肥的最高减量潜力研究

【目的】添加脲酶抑制剂（Urease inhibitor, UI）是提高肥料利用率的有效途径,在尿素（Urea,U）中添加1%的脲酶抑制剂NBPT（N-丁基硫代磷酰三胺）是目前研究使用证明效果最可靠的添加比例。针对当前稻田氮肥施用水平过高的问题,本文采用田间小区试验研究了目前脲酶抑制剂添加比例下稻田氮肥的减施潜力以及脲酶抑制剂的节肥增效机理。【方法】本试验在我国长江中下游的双季稻田进行,脲酶抑制剂用量NBPT为尿素用量的1%。尿素用量设五个水平为N 90、 112.5、 135、 157.5 和180 kg/hm2,分别依次记为U1、 U2、 U3、 U4和U5, 7个处理为CK（不施氮肥）、 U1+UI、 U2+UI、 U3+UI、 U4+UI、 U5+UI、 U5（U5为传统施氮量, N 180 kg/hm2为农民习惯施氮量）,三次重复。U1~U5处理施氮量分别是在农民习惯施氮量的基础上降低50%、 37.5%、 25%、 12.5%、 0%。通过取样分析水稻分蘖期和孕穗期各处理对土壤脲酶活性、 硝酸还原酶活性、 土壤铵态氮含量、 硝态氮含量以及微生物量碳、 氮的含量,研究NBPT对水稻两个主要生育期土壤氮素供应的影响,比较各处理的产量以及氮肥利用率来得出氮肥的减施潜力,在此基础上通过逐步回归分析研究以上各指标对产量的影响,探明脲酶抑制剂（NBPT）在双季稻田的增效机理。【结果】 1) 在双季稻田,添加NBPT后,施氮量为N 135 kg/hm2的籽粒产量达到最高。与传统施氮（单施尿素N 180 kg/hm2）处理相比,早、 晚稻可分别增产8.54%和12.87%,氮肥当季利用率分别提高6.78%和9.46%,可节约氮肥25%; 2)与传统施氮相比,添加NBPT显著降低了水稻分蘖期的土壤脲酶活性和铵态氮含量,显著提高了孕穗期的铵态氮含量,而对此时期的脲酶活性无显著影响,NBPT对两个时期的硝酸还原酶活性、 硝态氮含量及微生物量碳、 氮含量均无明显影响,可见基施的NBPT主要是降低尿素水解速率方面效果显著,并且NBPT具有时效性,其主要是在水稻孕穗期之前起作用,在生态上较为安全; 3) 从各项土壤指标与水稻产量相关性的逐步回归分析结果来看,水稻分蘖期与孕穗期稻田土壤中铵态氮含量对水稻产量影响显著,而且孕穗期的影响大于分蘖期,其余指标则对产量无明显影响。【结论】由于脲酶抑制剂NBPT减缓了分蘖期尿素的水解作用,提高了孕穗期土壤中的铵态氮含量,为水稻后期生长提供充足的氮肥,在双季稻减肥方面具有显著的效果。在本试验土壤条件下,尿素中添加1% 的NBPT,可在提高产量的同时,将传统施氮肥量减少25%,是适于稻田应用的脲酶抑制剂。     

High specific activity in low microbial biomass soils across a no-till evapotranspiration gradient in Colorado

The need to identify microbial community parameters that predict microbial activity is becoming more urgent, due to the desire to manage microbial communities for ecosystem services as well as the desire to incorporate microbial community parameters within ecosystem models. In dryland agroecosystems, microbial biomass C (MBC) can be increased by adopting alternative management strategies that increase crop residue retention, nutrient reserves, improve soil structure and result in greater water retention. Changes in MBC could subsequently affect microbial activities related to decomposition, C stabilization and sequestration. We hypothesized that MBC and potential microbial activities that broadly relate to decomposition (basal and substrate-induced respiration, N mineralization, and β-glucosidase and arylsulfatase enzyme activities) would be similarly affected by no-till, dryland winter wheat rotations distributed along a potential evapotranspiration (PET) gradient in eastern Colorado. Microbial biomass was smaller in March 2004 than in November 2003 (417 vs. 231 μg g⁻¹ soil), and consistently smaller in soils from the high PET soil (191 μg g⁻¹) than in the medium and low PET soils (379 and 398 μg g⁻¹, respectively). Among treatments, MBC was largest under perennial grass (398 μg g⁻¹). Potential microbial activities did not consistently follow the same trends as MBC, and the only activities significantly correlated with MBC were β-glucosidase (r = 0.61) and substrate-induced respiration (r = 0.27). In contrast to MBC, specific microbial activities (expressed on a per MBC basis) were greatest in the high PET soils. Specific but not total activities were correlated with microbial community structure, which was determined in a previous study. High specific activity in low biomass, high PET soils may be due to higher microbial maintenance requirements, as well as to the unique microbial community structure (lower bacterial-to-fungal fatty acid ratio and lower 17:0 cy-to-16:1ω7c stress ratio) associated with these soils. In conclusion, microbial biomass should not be utilized as the sole predictor of microbial activity when comparing soils with different community structures and levels of physiological stress, due to the influence of these factors on specific activity.     

Nitrogen losses from two grassland soils with different fungal biomass

Nitrogen losses from agricultural grasslands cause eutrophication of ground- and surface water and contribute to global warming and atmospheric pollution. It is widely assumed that soils with a higher fungal biomass have lower N losses, but this relationship has never been experimentally confirmed. With the increased interest in soil-based ecosystem services and sustainable management of soils, such a relationship would be relevant for agricultural management. Here we present a first attempt to test this relationship experimentally. We used intact soil columns from two plots from a field experiment that had consistent differences in fungal biomass (68 ± 8 vs. 111 ± 9 μg C g⁻¹) as a result of different fertilizer history (80 vs. 40 kg N ha⁻¹ y⁻¹ as farm yard manure), while other soil properties were very similar. We performed two greenhouse experiments: in the main experiment the columns received either mineral fertilizer N or no N (control). We measured N leaching, N₂O emission and denitrification from the columns during 4 weeks, after which we analyzed fungal and bacterial biomass and soil N pools. In the additional ¹⁵N experiment we traced added N in leachates, soil, plants and microbial biomass. We found that in the main experiment, N₂O emission and denitrification were lower in the high fungal biomass soil, irrespective of the addition of fertilizer N. Higher ¹⁵N recovery in the high fungal biomass soil also indicated lower N losses through dentrification. In the main experiment, N leaching after fertilizer addition showed a 3-fold increase compared to the control in low fungal biomass soil (11.9 ± 1.0 and 3.9 ± 1.0 kg N ha⁻¹, respectively), but did not increase in high fungal biomass soil (6.4 ± 0.9 after N addition vs. 4.5 ± 0.8 kg N ha⁻¹ in the control). Thus, in the high fungal biomass soil more N was immobilized. However, the ¹⁵N experiment did not confirm these results; N leaching was higher in high fungal biomass soil, even though this soil showed higher immobilization of ¹⁵N into microbial biomass. However, only 3% of total ¹⁵N was found in the microbial biomass 2 weeks after the mineral fertilization. Most of the recovered ¹⁵N was found in plants (approximately 25%) and soil organic matter (approximately 15%), and these amounts did not differ between the high and the low fungal biomass soil. Our main experiment confirmed the assumption of lower N losses in a soil with higher fungal biomass. The additional ¹⁵N experiment showed that higher fungal biomass is probably not the direct cause of higher N retention, but rather the result of low nitrogen availability. Both experiments confirmed that higher fungal biomass can be considered as an indicator of higher nitrogen retention in soils.     

Manipulating the N release from N labelled celery residues by using straw and vinasses

The aim of this laboratory study was to investigate the effect of straw and vinasses on the nitrogen (N) mineralization-immobilization turnover of celery residues during two periods (each simulating a time period from autumn till spring) under laboratory conditions. During the first period (1-198 d), ¹⁵N-labelled celery residues (1.1 g dry matter (DM) kg⁻¹ soil) were incubated together with straw (8.1 g DM kg⁻¹ soil), aiming to immobilize the N released from celery residues, followed by an incorporation of vinasses (1.9 g DM kg⁻¹ soil) after 84 d, with a view to remineralizing the immobilized celery-N. During the second period (198-380 d), the experimental set-up was repeated, except that non-labelled celery residues were used. Total N, mineral N and their ¹⁵N enrichments as well as microbial biomass N were determined at regular time intervals. During both periods, mixing celery residues with straw significantly increased microbial biomass N (90.5 and 40.5 mg N kg⁻¹ extra compared to celery only treatment) and decreased the amount of mineral N (reduction of 56.1 and 45.9 mg N kg⁻¹ soil compared to celery only treatment) and the celery-derived mineral ¹⁵N (0% of mineral celery-derived ¹⁵N in straw treatment compared to 35% of mineral celery-derived ¹⁵N in celery only treatment). After maximum immobilization, a natural remineralization (without addition of vinasses) of 32.2 (at day 198) and 11.1 mg N kg⁻¹ soil (at day 380) occurred in the straw treatment, but the mineral N content remained significantly lower than in the celery only treatment during the complete experiment, and the amount of remineralized celery-¹⁵N was very low (5.4% of celery-derived ¹⁵N after 380 d). Vinasses caused no real priming effect, although it did slightly increase the amount of remineralized celery-¹⁵N (+6.4% of celery-derived ¹⁵N at day 380 compared to the straw treatment), probably due an apparent added N interaction caused by displacement reactions with the soil microbial biomass.     

Nutrient limitation of litter decomposition with long-term secondary succession: evidence from controlled laboratory experiments

Purpose

Understanding ecosystem processes such as litter decomposition in response to dramatic land-use change is critical for modeling and predicting carbon (C) cycles. However, the patterns of litter decomposition along with long-term secondary succession (over 100 years) are not well reported, especially concerning nutrient limitations on litter decomposition.

Materials and methods

To clarify the response of litter decomposition to changes in soil nutrient availability, we conducted four incubation experiments involving soil and litter and nutrient addition from different successional stages and investigated the changes in microbial respiration and litter mass loss.

Results and discussion

Our results revealed that microbial respiration increased with succession without any litter addition (1.19~1.73 mg C g^?1 soil), and litter addition significantly promoted microbial respiration (16.5~72.9%), especially in the early successional stage (grassland and shrubland). The decomposition rate of the same litter decreased with succession. In addition, nitrogen (N) and phosphorus (P) addition showed significant effects on litter decomposition and microbial respiration; P addition promoted litter decomposition (2.4~15.3%) and microbial respiration (10.1~34.5%) in all successional stages, while N addition promoted litter decomposition (4.0~10.3%) and microbial respiration (5.4~27.2%) in all except the last stage of succession, which showed a negative effect on litter decomposition (??7.5%) and microbial respiration (??6.1%), indicating possible N saturation of litter decomposition and microbial respiration.

Conclusions

This work highlights that soil nutrient availability and successional stages need to be taken into account to predict the changes to litter decomposition in response to global changes.

     

Microbial immobilization and mineralization of dissolved organic nitrogen from forest floors

Dissolved organic nitrogen (DON) plays a key role in the N cycle of many ecosystems, as DON availability and biodegradation are important for plant growth, microbial metabolism and N transport in soils. However, biodegradation of DON (defined as the sum of mineralization and microbial immobilization) is only poorly understood. In laboratory incubations, biodegradation of DON and dissolved organic carbon (DOC) from Oi and Oa horizons of spruce, beech and cypress forests ranged from 6 to 72%. Biodegradation of DON and DOC was similar in most samples, and mineralization of DON was more important than microbial immobilization. Nitrate additions (0-10 mg N L⁻¹) never influenced either DON immobilization by microorganisms or mineralization. We conclude that soil microorganisms do not necessarily prefer mineral N over DON for meeting their N demand, and that biodegradation of DON seems to be driven by the microbial demand for C rather than N. Quantifying the dynamics of DON in soils should include consideration of both C and N demands by microbes.     

Effects of simulated nitrogen deposition on soil respiration components and their temperature sensitivities in a semiarid grassland

Nitrogen (N) deposition to semiarid ecosystems is increasing globally, yet few studies have investigated the ecological consequences of N enrichment in these ecosystems. Furthermore, soil CO₂ flux – including plant root and microbial respiration – is a key feedback to ecosystem carbon (C) cycling that links ecosystem processes to climate, yet few studies have investigated the effects of N enrichment on belowground processes in water-limited ecosystems. In this study, we conducted two-level N addition experiments to investigate the effects of N enrichment on microbial and root respiration in a grassland ecosystem on the Loess Plateau in northwestern China. Two years of high N additions (9.2 g N m⁻² y⁻¹) significantly increased soil CO₂ flux, including both microbial and root respiration, particularly during the warm growing season. Low N additions (2.3 g N m⁻² y⁻¹) increased microbial respiration during the growing season only, but had no significant effects on root respiration. The annual temperature coefficients (Q₁₀) of soil respiration and microbial respiration ranged from 1.86 to 3.00 and 1.86 to 2.72 respectively, and there was a significant decrease in Q₁₀ between the control and the N treatments during the non-growing season but no difference was found during the growing season. Following nitrogen additions, elevated rates of root respiration were significantly and positively related to root N concentrations and biomass, while elevated rates of microbial respiration were related to soil microbial biomass C (SMBC). The microbial respiration tended to respond more sensitively to N addition, while the root respiration did not have similar response. The different mechanisms of N addition impacts on soil respiration and its components and their sensitivity to temperature identified in this study may facilitate the simulation and prediction of C cycling and storage in semiarid grasslands under future scenarios of global change.     

Nitrogen addition enhances home-field advantage during litter decomposition in subtropical forest plantations

Nitrogen (N) exerts strong effects on litter decomposition through altering microbial abundance and community composition. However, the effect of N addition on plant–soil interactions such as home-field advantage (HFA: enhanced decomposition at a home environment compared to a guest environment) in relation to litter decomposition remains unclear. To fill this knowledge gap, we conducted a reciprocal litter transplant plus N addition experiment in Mytilaria laosensis and Cunninghamia lanceolata plantations for two years in subtropical China where anthropogenic N input is amongst the highest in the world. We found positive HFA effects (in which the calculation incorporates litter of both species) with litter mass loss 11.2% faster at home than in the guest environment in the N addition (50 kg N ha⁻¹ yr⁻¹) treatment, but no significant HFA effects were found in the control treatment. The magnitude of the HFA effect on carbon (C) release increased with N addition, while that on N release decreased. The HFA effects on phosphorus, potassium, calcium, sodium, and magnesium release were positive overall, but varied through time and the magnitude of the effects were different among elements. The greater HFA effects in the N addition treatment were associated with greater differences in microbial biomass and community composition between home and guest environments than in the control treatment. Our results indicate that anthropogenic N enrichment could lead to enhanced HFA effects, through modification of microbial communities, and thereby affect C sequestration and N cycling in subtropical forests.     

Non-linear response of microbial activity across a gradient of nitrogen addition to a soil from the Gurbantunggut Desert,northwestern China

Identifying the patterns of soil microbial responses to increasing nitrogen (N) availability are important since microbial processes are related to the potential nutrient transformations. The effects of the addition of N to the soil microbial community of the Gurbantunggut Desert, China, are described in this paper. The study was conducted over a two-year period with trials commencing at the beginning of each growing season. Soil enzyme activity, microbial biomass and microbial community level physiological profile (CLPP) were determined at 0–5 cm and 5–10 cm soil depths. Nitrogen was added to the soil at five rates plus a control, i.e. 0, 0.5, 1, 3, 6 and 24 g N m⁻² y⁻¹. We hypothesized that soil enzyme activities and microbial biomass N (MBN) would firstly increase and then decrease, and CLPP would be altered with increasing N addition, due to the deleterious effects of higher N addition upon microbial activity. Because of the relatively higher organic matter in the upper depth of soil layers, we further hypothesized that the responses of microbial activities in the 0–5 cm depth would be more marked than at 5–10 cm. In partial support of our hypothesis, soil enzyme activities, microbial biomass and nutrient concentrations responded to N addition with the most significant changes occurring in the 0–5 cm soil depth. Addition of N resulted in an increase in MBN and a decrease in urease activity. Invertase and alkaline phosphatase (AlP) activities increased at low doses of N addition and showed a decrease at higher doses. There was no evidence of change in oxidative enzyme activity at low N treatments but activity decreased at high N additions. However, the CLPP was not affected by N addition. The results of this study suggest that N supplementation in this desert soil may affect C transformation, increase availability of N and P, and immobilize N in the microbial biomass. Responses of the enzyme activity to N supplementation occurred within the context of an apparently stable or unresponsive microbial community structure.     

Dynamics of soil amino sugar pools during decomposition processes of corn residues as affected by inorganic N addition

Purpose  

Identifying the impact of inorganic-nitrogen (N) availability on soil amino sugar dynamics during corn (Zea mays L.) residue decomposition may advance our knowledge of microbial carbon (C) and N transformations and the factors controlling these processes in soils. Amino sugars are routinely used as microbial biomarkers to investigate C and N sequestration in microbial residues, and they are also involved in microbial-mediated soil organic matter (SOM) turnover. We conducted a 38-week incubation study using a Mollisol which was amended with corn residues and four levels of inorganic N (i.e., 0, 60.3, 167.2, and 701.9 mg N kg⁻¹ soil). The objective of this study was to examine the effects of inorganic-N availability on fungal and bacterial formation and stabilization of heterogeneous amino sugars during the corn residue decomposition in soil.     

Fate of Chinese-fir litter during decomposition as a result of inorganic N additions

We conducted a controlled experiment to evaluate Chinese-fir litter decomposition and its response to the addition of inorganic N. Litter-derived CO₂, microbial biomass carbon (MBC), and dissolved organic carbon (DOC) were monitored during an 87-d incubation of a mixed soil–litter substrate using the ¹³C tracer technique. Litter C was mostly converted to CO₂ (47.4% of original mass), followed by MBC (3.6%), and DOC (1.0%), with 48% remaining unaltered in the soil. The litter decomposition rate significantly increased with the addition of inorganic N, although the effect depended on whether N was added as NH₄⁺ or NO₃⁻. Soil-derived CO₂, MBC, and DOC also increased following the combined addition of litter and N. The results showed that only a small percentage of litter C was retained as MBC or DOC and that the conversion rate depended, in part, on the form of inorganic N added to the Chinese-fir plantation soil.     

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.     

Effects of organic matter addition on phosphorus availability to flooded and nonflooded rice in a P‐deficient tropical soil: a greenhouse study

Addition of organic matter (OM) to flooded soils stimulates reductive dissolution of Fe(III) minerals, thereby mobilizing associated phosphate (P). Hence, OM management has the potential to overcome P deficiency. This study assessed if OM applications increases soil or mineral fertilizer P availability to rice under anaerobic (flooded) condition and if that effect is different relative to that in aerobic (nonflooded) soils. Rice was grown in P‐deficient soil treated with combinations of addition of mineral P (0, 26 mg P/kg), OM (0, ~9 g OM/kg as rice straw + cattle manure) and water treatments (flooded vs nonflooded) in a factorial pot experiment. The OM was either freshly added just before flooding or incubated moist in soil for 6 months prior to flooding; blanket N and K was added in all treatments. Fresh addition of OM promoted reductive dissolution of Fe(III) minerals in flooded soils, whereas no such effect was found when OM had been incubated for 6 months before flooding. Yield and shoot P uptake largely increased with mineral P addition in all soils, whereas OM addition increased yield and P uptake only in flooded soils following fresh OM addition. The combination of mineral P and OM gave the largest yield and P uptake. Addition of OM just prior to soil flooding increased P uptake but was insufficient to overcome P deficiency in the absence of mineral P. Larger applications of OM are unlikely to be more successful in flooded soils due to side effects, such as Fe toxicity.     

Effect of land use types on decomposition of 14C-labelled maize residue (Zea mays L.)

The effect of three land use types on decomposition of ¹⁴C-labelled maize (Zea mays L.) residues and soil organic matter were investigated under laboratory conditions. Samples of three Dystric Cambisols under plow tillage (PT), reduced tillage (RT) and grassland (GL) collected from the upper 5 cm of the soil profile were incubated for 159 days at 20 °C with or without ¹⁴C-labelled maize residue. After 7 days cumulative CO₂ production was highest in GL and lowest in PT, reflecting differences in soil organic C (SOC) concentration among the three land use types and indicating that mineralized C is a sensitive indicator of the effects of land use regime on SOC. ¹⁴CO₂ efflux from maize residue decomposition was higher in GL than in PT, possibly due to higher SOC and microbial biomass C (MBC) in GL than in PT. ¹⁴CO₂ efflux dynamics from RT soil were different from those of PT and GL. RT had the lowest ¹⁴CO₂ efflux from days 2 to 14 and the highest from days 28 to 159. The lowest MBC in RT explained the delayed decomposition of residues at the beginning. A double exponential model gave a good fit to the mineralization of SOC and residue-¹⁴C (R² > 0.99) and allowed estimation of decomposition rates as dependent on land use. Land use affected the decomposition of labile fractions of SOC and of maize residue, but had no effect on the decomposition of recalcitrant fractions. We conclude that land use affected the decomposition dynamics within the first 1.5 months mainly because of differences in soil microbial biomass but had low effect on cumulative decomposition of maize residues within 5 months.     

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.     

Soil microbial properties under N and P additions in a semi-arid, sandy grassland

Surface (0–15 cm) soil samples were collected from a semi-arid, sandy grassland in Keerqin Sandy Lands, Northeast China to study changes in soil microbial and chemical properties after five consecutive years of nitrogen (N) and phosphorus (P) additions. Nitrogen and P additions and their interactions negligibly affected soil organic carbon and total N contents, while P addition significantly increased soil total P content. Soil pH was significantly decreased by N addition, which significantly increased net nitrification rate, whereas it did not affect net N mineralization rate. No significant effects of N and P additions and their interactions on basal respiration were detected. In addition, N addition significantly decreased microbial biomass C (MBC) and N, and thus microbial quotient, but increased dissolved organic C and microbial metabolic quotient due to the significant decrease of MBC. Our results suggest that in the mid-term the addition of N, but not P, can change soil microbial properties, with a possible decline in soil quality of semi-arid, sandy grasslands.     

Relationships between C and N availability, substrate age, and natural abundance C and N signatures of soil microbial biomass in a semiarid climate

Soil microbial organisms are central to carbon (C) and nitrogen (N) transformations in soils, yet not much is known about the stable isotope composition of these essential regulators of element cycles. We investigated the relationship between C and N availability and stable C and N isotope composition of soil microbial biomass across a three million year old semiarid substrate age gradient in northern Arizona. The δ¹⁵N of soil microbial biomass was on average 7.2‰ higher than that of soil total N for all substrate ages and 1.6‰ higher than that of extractable N, but not significantly different for the youngest and oldest sites. Microbial ¹⁵N enrichment relative to soil extractable and total N was low at the youngest site, increased to a maximum after 55,000 years, and then decreased slightly with age. The degree of ¹⁵N enrichment of microbial biomass correlated negatively with the C:N mass ratio of the soil extractable pool. The δ¹³C signature of soil microbial biomass was 1.4‰ and 4.6‰ enriched relative to that of soil total and extractable pools respectively and showed significant differences between sites. However, microbial ¹³C enrichment was unrelated to measures of C and N availability. Our results confirm that ¹⁵N, but not ¹³C enrichment of soil microbial biomass reflects changes in C and N availability and N processing during long-term ecosystem development.