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1.
Microbial immobilization/mineralization and mineral fixation/release of ammonium are important for N retention and supply. However, the rates of such processes vary among different fertility soils and fertilization management practices. Three long-term different fertilized soils were used to simulate a range in soil fertility level and incubated with different N amendments for 144 days. The dynamics of 15N derived from ammonium sulfate (AS) or straw in different soil N pools and the ammonium sulfate-N or straw-N retention and supply were studied. In the absence of straw, the amount of ammonium sulfate-N present as fixed ammonium was 1.1–3.5-fold higher than that present as soil microbial biomass N (SMBN), although ammonium sulfate-derived SMBN and its mineralization increased by increasing soil fertility level. Straw addition significantly (P < 0.05) enhanced the relative importance of the SMBN pool on ammonium sulfate-N retention and supply compared with the fixed ammonium-N pool, and the former exceeded the latter in higher fertility soils. Regardless of soil fertility levels, straw addition significantly blocked the release of ammonium sulfate-N from the fixed ammonium-N pool. The SMBN pool was more important in straw-N retention and supply than the fixed ammonium-N pool, confirming that straw-N cycling depended more on biotic processes. The percentage of mineralized ammonium sulfate-N or straw-N from SMBN was higher than that released from fixed ammonium, indicating the higher availability of SMBN. Generally, the mineral fixation/release of ammonium was the main process for mineral fertilizer N retention and supply in the low fertility soil with or without straw addition, whereas microbial immobilization/mineralization became the main process in the high fertility soil with straw addition. Our results gave insights on the ammonium sulfate-N or straw-N retention and supply in different fertility soils, providing suggestions for optimizing straw management and synchronizing N supply with crop demand.  相似文献   

2.
Soil microbes are frequently limited by carbon (C), but also have a high phosphorus (P) requirement. Little is known about the effect of P availability relative to the availability of C on soil microbial activity. In two separate experiments, we assessed the effect of P addition (20 mg P kg?1 soil) with and without glucose addition (500 mg C kg?1 soil) on gross nitrogen (N) mineralization (15N pool dilution method), microbial respiration, and nitrous oxide (N2O) emission in a grassland soil. In the first experiment, soils were incubated for 13 days at 90% water holding capacity (WHC) with addition of NO3? (99 mg N kg?1 soil) to support denitrification. Addition of C and P had no effect on gross N mineralization. Initially, N2O emission significantly increased with glucose, but it decreased at later stages of the incubation, suggesting a shift from C to NO3? limitation of denitrifiers. P addition increased the N2O/CO2 ratio without glucose but decreased it with glucose addition. Furthermore, the 15N recovery was lowest with glucose and without P addition, suggesting a glucose by P interaction on the denitrifying community. In the second experiment, soils were incubated for 2 days at 75% WHC without N addition. Glucose addition increased soil 15N recovery, but had no effect on gross N mineralization. Possibly, glucose addition increased short-term microbial N immobilization, thereby reducing N-substrates for nitrification and denitrification under more aerobic conditions. Our results indicate that both C and P affect N transformations in this grassland soil.  相似文献   

3.
Soil moisture changes, arising from seasonal variation or from global climate changes, could influence soil nitrogen (N) transformation rates and N availability in unfertilized subtropical forests. A 15?N dilution study was carried out to investigate the effects of soil moisture change (30–90 % water-holding capacity (WHC)) on potential gross N transformation rates and N2O and NO emissions in two contrasting (broad-leaved vs. coniferous) subtropical forest soils. Gross N mineralization rates were more sensitive to soil moisture change than gross NH4 + immobilization rates for both forest soils. Gross nitrification rates gradually increased with increasing soil moisture in both forest soils. Thus, enhanced N availability at higher soil moisture values was attributed to increasing gross N mineralization and nitrification rates over the immobilization rate. The natural N enrichment in humid subtropical forest soils may partially be due to fast N mineralization and nitrification under relatively higher soil moisture. In broad-leaved forest soil, the high N2O and NO emissions occurred at 30 % WHC, while the reverse was true in coniferous forest soil. Therefore, we propose that there are different mechanisms regulating N2O and NO emissions between broad-leaved and coniferous forest soils. In coniferous forest soil, nitrification may be the primary process responsible for N2O and NO emissions, while in broad-leaved forest soil, N2O and NO emissions may originate from the denitrification process.  相似文献   

4.
Abstract

A micro-plot 15N-tracer experiment was established in three different soils of a long-term soil fertility field experiment. The nutrient-poor loam sand has been subjected to various treatments over the years and this has resulted in different organic C (0.35% – 0.86%), microbial biomass (38.3 – 100.0 µg C mic g?1 soil), clay and fine silt contents. Using the 15N-pool dilution technique, we assessed gross N-transfer rates in the field. Gross N mineralization rates varied strongly among the three plots and ranged between 0.4 and 4.2 µg N g?1 soil d?1. Gross nitrification rates were estimated to be between 0 and 2.1 µg N g?1 soil d?1. No correlation between gross N mineralization rates and the organic matter content of the soils was established. However, gross nitrate consumption rates increased with increasing soil C content. The 15N-pool dilution technique was successfully used to measure gross N transfer rates directly in the field.  相似文献   

5.
Microbial mineralization and immobilization of nutrients strongly influence soil fertility. We studied microbial biomass stoichiometry, microbial community composition, and microbial use of carbon (C) and phosphorus (P) derived from glucose-6-phosphate in the A and B horizons of two temperate Cambisols with contrasting P availability. In a first incubation experiment, C, nitrogen (N) and P were added to the soils in a full factorial design. Microbial biomass C, N and P concentrations were analyzed by the fumigation-extraction method and microbial community composition was analyzed by a community fingerprinting method (automated ribosomal intergenic spacer analysis, ARISA). In a second experiment, we compared microbial use of C and P from glucose-6-phosphate by adding 14C or 33P labeled glucose-6-phosphate to soil. In the first incubation experiment, the microbial biomass increased up to 30-fold due to addition of C, indicating that microbial growth was mainly C limited. Microbial biomass C:N:P stoichiometry changed more strongly due to element addition in the P-poor soils, than in the P-rich soils. The microbial community composition analysis showed that element additions led to stronger changes in the microbial community in the P-poor than in the P-rich soils. Therefore, the changed microbial biomass stoichiometry in the P-poor soils was likely caused by a shift in the microbial community composition. The total recovery of 14C derived from glucose-6-phosphate in the soil microbial biomass and in the respired CO2 ranged between 28.2 and 37.1% 66 h after addition of the tracer, while the recovery of 33P in the soil microbial biomass was 1.4–6.1%. This indicates that even in the P-poor soils microorganisms mineralized organic P and took up more C than P from the organic compound. Thus, microbial mineralization of organic P was driven by microbial need for C rather than for P. In conclusion, our experiments showed that (i) the microbial biomass stoichiometry in the P-poor soils was more susceptible to additions of C, N and P than in the P-rich soils and that (ii) even in the P-poor soils, microorganisms were C-limited and the mineralization of organic P was mainly driven by microbial C demand.  相似文献   

6.
 Gross rates of soil processes and microbial activity were measured in two grazed permanent pasture soils which had recently been amended with N fertilizer or dung. 15N studies of rates of soil organic matter turnover showed gross N mineralization was higher, and gross N immobilization was lower, in a long-term fertilized soil than in a soil which had never received fertilizer N. Net mineralization was also found to be higher in the fertilized soil: a consequence of the difference between the opposing N turnover processes of N mineralization and immobilization. In both soils without amendments the soil microbial biomass contents were similar, but biomass activity (specific respiration) was higher in the fertilized soil. Short-term manipulation of fertilizer N input, i.e. adding N to unfertilized soil, or witholding N from previously fertilized soil, for one growing season, did not affect gross mineralization, immobilization or biomass size and activity. Amendments of dung had little effect on gross mineralization, but there was an increase in immobilization in both soils. Total biomass also increased under dung in the unfertilized soil, but specific respiration was reduced, suggesting changes in the composition of the biomass. Dung had a direct effect on the microbial biomass by temporarily increasing available soil C. Prolonged input of fertilizer N increases soil C indirectly as a result of enhanced plant growth, the effect of which may not become evident within one seasonal cycle. Received: 18 December 1998  相似文献   

7.
In forest soils where a large fraction of total phosphorus (P) is in organic forms, soil micro-organisms play a major role in the P cycle and plant availability since they mediate organic P transformations. However, the correct assessment of organic P mineralization is usually a challenging task because mineralized P is rapidly sorbed and most mineralization fluxes are very weak. The objectives of the present work were to quantify in five forest Spodosols at soil depths of 0-15 cm net mineralization of total organic P and the resulting increase in plant available inorganic P and to verify whether net or gross P mineralization could be estimated using the C or N mineralization rates. Net mineralization of total organic P was derived from the net changes in microbial P and gross mineralization of P in dead soil organic matter. We studied very low P-sorbing soils enabling us to use lower extractants to assess the change in total inorganic P as a result of gross mineralization of P in dead soil organic matter. In addition, to enable detection of gross mineralization of P in dead soil organic matter, a long-term incubation (517 days) experiment was carried out. At the beginning of the experiment, total P contents of the soils were very low (19-51 μg g−1) and were essentially present as organic P (17-44 μg g−1, 85-91%) or microbial P (6-14 μg g−1; 24-39%). Conversely, the initial contents of inorganic P were low (2-7 μg g−1; 9-15%). The net changes in the pool size of microbial P during the 517 days of incubation (4-8 μg g−1) and the amounts of P resulting from gross mineralization of dead soil organic matter (0.001-0.018 μg g−1 day−1; 0.4-9.5 μg g−1 for the entire incubation period) were considerable compared to the initial amounts of organic P and also when compared to the initial diffusive iP fraction (<0.3 μg g−1). Diffusive iP corresponds to the phosphate ions that can be transferred from the solid constituents to the soil solution under a gradient of concentration. Net mineralization of organic P induced an important increase in iP in soil solution (0.6-10 μg g−1; 600-5000% increase) and lower increases in diffusive iP fractions (0.3-5 μg g−1; 300-2000% increase), soil solid constituents having an extremely low reactivity relative to iP. Therefore, soil micro-organisms and organic P transformations play a major role in the bioavailability of P in these forest soils. In our study, the dead soil organic matter was defined as a recalcitrant organic fraction. Probably because gross mineralization of P from this recalcitrant organic fraction was mainly driven by the micro-organisms’ needs for energy, the rates of gross mineralization of C, N and P in the recalcitrant organic fraction were similar. Indirect estimation of gross mineralization of P in dead soil organic matter using the gross C mineralization rate seems thus an alternative method for the studied soils. However, additional studies are needed to verify this alternative method in other soils. No relationships were found between microbial P release and microbial C and N releases.  相似文献   

8.
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.  相似文献   

9.
Accurate prediction of soil N availability requires a sound understanding of the effects of environmental conditions and management practices on the microbial activities involved in N mineralization. We determined the effects of soil temperature and moisture content and substrate type and quality (resulting from long-term pasture management) on soluble organic C content, microbial biomass C and N contents, and the gross and net rates of soil N mineralization and nitrification. Soil samples were collected at 0–10 cm from two radiata pine (Pinus radiata D. Don) silvopastoral treatments (with an understorey pasture of lucerne, Medicago sativa L., or ryegrass, Lolium perenne L.) and bare ground (control) in an agroforestry field experiment and were incubated under three moisture contents (100, 75, 50% field capacity) and three temperatures (5, 25, 40 °C) in the laboratory. The amount of soluble organic C released at 40 °C was 2.6- and 2.7-fold higher than the amounts released at 25 °C and 5 °C, respectively, indicating an enhanced substrate decomposition rate at elevated temperature. Microbial biomass C:N ratios varied from 4.6 to 13.0 and generally increased with decreasing water content. Gross N mineralization rates were significantly higher at 40 °C (12.9 g) than at 25 °C (3.9 g) and 5 °C (1.5 g g–1 soil day–1); and net N mineralization rates were also higher at 40 °C than at 25 °C and 5 °C. The former was 7.5-, 34-, and 29-fold higher than the latter at the corresponding temperature treatments. Gross nitrification rates among the temperature treatments were in the order 25 °C >40 °C >5 °C, whilst net nitrification rates were little affected by temperature. Temperature and substrate type appeared to be the most critical factors affecting the gross rates of N mineralization and nitrification, soluble organic C, and microbial biomass C and N contents. Soils from the lucerne and ryegrass plots mostly had significantly higher gross and net mineralization and nitrification rates, soluble organic C, and microbial biomass C and N contents than those from the bare ground, because of the higher soil C and N status in the pasture soils. Strong positive correlations were obtained between gross and net rates of N mineralization, between soluble organic C content and the net and gross N mineralization rates, and between microbial biomass N and C contents.  相似文献   

10.
Application of crop residues and its biochar produced through slow pyrolysis can potentially increase carbon (C) sequestration in agricultural production systems. The impact of crop residue and its biochar addition on greenhouse gas emission rates and the associated changes of soil gross N transformation rates in agricultural soils are poorly understood. We evaluated the effect of wheat straw and its biochar applied to a Black Chernozemic soil planted to barley, two growing seasons or 15 months (at the full-bloom stage of barley in the second growing season) after their field application, on CO2 and N2O emission rates, soil inorganic N and soil gross N transformation rates in a laboratory incubation experiment. Gross N transformation rates were studied using the 15N isotope pool dilution method. The field experiment included four treatments: control, addition of wheat straw (30 t ha?1), addition of biochar pyrolyzed from wheat straw (20 t ha?1), and addition of wheat straw plus its biochar (30 t ha?1 wheat straw + 20 t ha?1 biochar). Fifteen months after their application, wheat straw and its biochar addition increased soil total organic C concentrations (p?=?0.039 and <0.001, respectively) but did not affect soil dissolved organic C, total N and NH4 +-N concentrations, and soil pH. Biochar addition increased soil NO3 ?-N concentrations (p?=?0.004). Soil CO2 and N2O emission rates were increased by 40 (p?p?=?0.03), respectively, after wheat straw addition, but were not affected by biochar application. Straw and its biochar addition did not affect gross and net N mineralization rates or net nitrification rates. However, biochar addition doubled gross nitrification rates relative to the control (p?2 and N2O emissions and enhance soil C sequestration. However, the implications of the increased soil gross nitrification rate and NO3 ?-N in the biochar addition treatment for long-term NO3 ?-N dynamics and N2O emissions need to be further studied.  相似文献   

11.
The dominant pools of C and N in the terrestrial biosphere are in soils, and understanding what factors control the rates at which these pools cycle is essential in understanding soil CO2 production and N availability. Many previous studies have examined large scale patterns in decomposition of C and N in plant litter and organic soils, but few have done so in mineral soils, and fewer have looked beyond ecosystem specific, regional, or gradient-specific drivers. In this study, we examined the rates of microbial respiration and net N mineralization in 84 distinct mineral soils in static laboratory incubations. We examined patterns in C and N pool sizes, microbial biomass, and process rates by vegetation type (grassland, shrubland, coniferous forest, and deciduous/broadleaf forest). We also modeled microbial respiration and net N mineralization in relation to soil and site characteristics using structural equation modeling to identify potential process drivers across soils. While we did not explicitly investigate the influence of soil organic matter quality, microbial community composition, or clay mineralogy on microbial process rates in this study, our models allow us to put boundaries on the unique explanatory power these characteristics could potentially provide in predicting respiration and net N mineralization. Mean annual temperature and precipitation, soil C concentration, microbial biomass, and clay content predicted 78% of the variance in microbial respiration, with 61% explained by microbial biomass alone. For net N mineralization, only 33% of the variance was explained, with mean annual precipitation, soil C and N concentration, and clay content as the potential drivers. We suggest that the high R2 for respiration suggests that soil organic matter quality, microbial community composition, and clay mineralogy explain at most 22% of the variance in respiration, while they could explain up to 67% of the variance in net N mineralization.  相似文献   

12.
High nitrogen (N) input often induces soil carbon (C) limitation, eutrophication of macronutrients, deficiency of base cations, and accumulation of toxic micronutrients. These changes are perceived to be critical factors in regulating soil C mineralization. Previous studies primarily focused on the individual effects of C, macronutrients, exchangeable base cations, and micronutrients on soil C mineralization. However, the relative importance of those factors in regulating soil C mineralization, especially in N-enriched ecosystems, remains unclear. To disentangle the relative contributions of aforementioned factors, lime and/or glucose were added to soils that were collected from a field experiment with historical N addition (6 years) at seven rates (0–50 g N m−2 year−1) in a grassland ecosystem. Lime and glucose were added to improve the soil C and key nutrient conditions. The responses of soil C mineralization rate to changes in soil C and macronutrients (N and P), exchangeable base cations (K+, Na+ and Mg2+), and micronutrients (Fe2+, Mn2+, Cu2+ and Zn2+) were examined. We found that lime addition decreased soil micronutrients, while glucose addition improved the soil available P and exchangeable base cations, especially at high historical N addition rates. The soil C mineralization was weakly associated with changes in soil nutrients, including the availability of N, P, exchangeable base cations, and micronutrients, which were conventionally and previously considered as the vital drivers of soil C mineralization. However, soil C mineralization strongly increased with glucose-induced enhancement of C availability and the subsequent enhancement of microbial biomass under increasing N addition rates. Based on the Structural Equation Model, the standardized total effects of C, macronutrients (N and P), base cations and micronutrients on soil C mineralization were 0.86, − 0.29, 0.15 and − 0.08, respectively. Findings from this study demonstrated that the N-induced significant changes in soil nutrients (e.g., eutrophication of N and P, base cations deficiency and accumulation of toxic macronutrients) mediated soil C mineralization, with C availability being the most critical driver for C mineralization in N-enriched soil. This study provides insight into the mechanistic understanding of the relationship between N input and terrestrial C cycling.  相似文献   

13.

Purpose

Alpine ecosystems on the Qinghai-Tibetan Plateau are sensitive to global climatic changes. However, the effects of temperature change resulting from global warming or seasonal variation on soil N availability in those ecosystems are largely unknown.

Materials and methods

We therefore conducted a 15N tracing study to investigate the effects of various temperatures (5–35 °C) on soil gross N transformation rates in an alpine meadow (AM) soil on the Qinghai-Tibetan Plateau. A natural secondary coniferous forest (CF) soil from the subtropical region was chosen as a reference to compare the temperature sensitivity of soil gross N transformation rates between alpine meadow and coniferous forest.

Results and discussion

Our results showed that increasing temperature increased gross N mineralization and NH4 + immobilization rates and overall enhanced N availability for plants in both soils. However, both rates in the CF soil were less sensitive to a temperature change from 5 to 15 °C compared to the AM soil. In both soils, different N retention mechanisms could have been operating with respect to changing temperatures in the different climatic regions. In the CF soil, the absence of NO3 ? production at all incubation temperatures suggests that in the subtropical soil which is characterized by high rainfall, an increase in N availability due to increasing temperature could be completely retained in soils. In contrast, the AM soil may be vulnerable to N losses with respect to temperature changes, in particular at 35 °C, in which higher nitrification rates were coupled with lower NH4 + and NO3 ? immobilization rates.

Conclusions

Our results suggest that increased soil temperature arising from global warming and seasonal variations will most likely enhance soil N availability for plants and probably increase the risk of N losses in the alpine meadow on the Qinghai-Tibetan Plateau.
  相似文献   

14.
A field study was conducted to investigate the long-term effect of surface application of sewage sludge composts vs chemical N fertilizer on total N, total C, soluble organic C, pH, EC, microbial biomass C and N, protease activity, deaminase activity, urease activity, gross and net rates of N mineralization and nitrification, CO2 evolution, and N2O production. Soil samples were taken from five depths (0–15, 15–20, 20–30, 30–40, and 40–50 cm) of a long-term experiment at the University of Tokyo, Japan. Three fields have been receiving sewage sludge composted with rice husk (RH), sawdust (SD), or mixed chemical fertilizer NPK (CF), applied at the rate of 240 kg N ha–1 each in split applications in summer and autumn since 1978. Significantly higher amounts of total N and C and soluble organic C were found in the compost than in the CF treatments up to the 40-cm soil depth, indicating improved soil quality in the former. In the CF treatment, soil pH values were significantly lower and electrical conductivity values were significantly higher than those of compost-treated soils of up to 50 cm depth. Soil microbial biomass C and N, CO2 evolution, protease, deaminase, and urease activities were significantly higher in the compost than in the CF treatments due to greater availability of organic substrates that stimulated microbial activity. Gross N mineralization rates determined by 15N dilution technique were eight and five times higher in the SD and RH treatments than in the CF treatment, respectively, probably due to high levels of microbial and enzyme activities. Net N mineralization rates were also significantly higher in the compost treatments and were negative in the CF treatment indicating immobilization. Net nitrification rates were higher in compost treatments and negative in the CF treatment. Nitrous oxide productions from compost treatments were higher than the CF treatment due to the greater availability of mineral N as a result of higher mineralization and nitrification rates and soluble organic C in the former. Most of the measured parameters were highest in the surface soil (0–15 cm) and were significantly higher in the SD treatment than in the RH treatment.  相似文献   

15.
Gross phosphorus (P) fluxes measured in isotopic dilution studies with 33P labeled soils include the biological processes of microbial P immobilization, remineralization of immobilized P and mineralization of non-microbial soil organic P. In this approach, isotopic dilution due to physicochemical processes is taken into account. Our objectives were to assess the effect of inorganic P availability on gross P mineralization and immobilization in soil under permanent grassland, and to relate these fluxes to soil respiration, phosphatase activity and substrate availability as assessed by an enzyme addition method. We used soils from an 18-year-old grassland fertilization experiment near Zurich, Switzerland, that were collected in two treatments which differed only in the amount of mineral P applied (0 and 17 kg P ha−1 yr−1 in NK and NPK, respectively). Water-extractable phosphate was low (0.1 and 0.4 mg P kg−1 soil in NK and NPK, while hexanol-labile (microbial) P was high (36 and 54 mg P kg−1 soil in NK and NPK). Extremely fast microbial P uptake under P-limited conditions in NK necessitated the use of a microbial inhibitor when determining isotopic dilution due to physicochemical processes. At the higher inorganic P availability in NPK, however, isotopic exchange parameters were similar in the presence and absence of a microbial inhibitor. Phosphatase activity was higher in NK than in NPK, while soil respiration, water-extractable organic P and its enzyme-labile fraction were not affected by P status. Together, the results showed that inorganic P availability primarily affected microbial P immobilization which was the main component of gross P fluxes in both treatments. Gross P mineralization rates (8.2 and 3.1 mg P kg−1 d−1 for NK and NPK) during the first week were higher than reported in other studies on arable and forest soils and at least equal to isotopically exchangeable P due to physicochemical processes, confirming the importance of microbial processes in grassland soils.  相似文献   

16.
We examined the impact of long-term cattle grazing on soil processes and microbial activity in a temperate salt marsh. Soil conditions, microbial biomass and respiration, mineralization and denitrification rates were measured in upper salt marsh that had been ungrazed or cattle grazed for several decades. Increased microbial biomass and soil respiration were observed in grazed marsh, most likely stimulated by enhanced rates of root turnover and root exudation. We found a significant positive effect of grazing on potential N mineralization rates measured in the laboratory, but this difference did not translate to in situ net mineralization measured monthly from May to September. Rates of denitrification were lowest in the grazed marsh and appeared to be limited by nitrate availability, possibly due to more anoxic conditions and lower rates of nitrification. The major effect of grazing on N cycling therefore appeared to be in limiting losses of N through denitrification, which may lead to enhanced nutrient availability to saltmarsh plants, but a reduced ability of the marsh to act as a buffer for land-derived nutrients to adjacent coastal areas. Additionally, we investigated if grazing influences the rates of turnover of labile and refractory C in saltmarsh soils by adding 14C-labelled leaf litter or root exudates to soil samples and monitoring the evolution of 14CO2. Grazing had little effect on the rates of mineralization of 14C used as a respiratory substrate, but a larger proportion of 14C was partitioned into microbial biomass and immobilized in long- and medium-term storage pools in the grazed treatment. Grazing slowed down the turnover of the microbial biomass, which resulted in longer turnover times for both leaf litter and root exudates. Grazing may therefore affect the longevity of C in the soil and alter C storage and utilization pathways in the microbial community.  相似文献   

17.
Purple soils (Eutric Regosols) are widely distributed in humid subtropical Southwest China. They are characterized by high nitrification activities, with risks of severe NO3? leaching. Incorporation of crop residues is considered an effective method to reduce NO3? loss. In the present study, we compared the effects of alfalfa, rice straw, and sugarcane bagasse on gross N transformation turnover in a purple soil (purple soil, pH 7.62) compared with those in an acid soil (acid soil, pH 5.26), at 12 h, 3 months, and 6 months after residue incorporation. The gross N transformation rates were determined by 15N tracing. All tested crop residues stimulated the gross N mineralization rates, but reduced the net mineralization rates in both soils at 12 h after residue incorporation; however, the extent of the effect varied with the crop residue qualities, with rice straw having the strongest effects. Crop residues reduced net nitrification rates by depressing gross autotrophic nitrification rates and stimulating NO3? immobilization rates in the purple soil, particularly after rice straw incorporation (net nitrification rate decreased from 16.72 mg N kg?1 d?1 in the control to ??29.42 mg N kg?1 d?1 at 12 h of residue incorporation); however, crop residues did not affect the gross autotrophic nitrification rates in the acid soil. Crop residue effects subsided almost completely within 6 months, with sugarcane bagasse showing the longest lasting effects. The results indicated that crop residues affected the N transformation rates in a temporal manner, dependent on soil properties and residue qualities.  相似文献   

18.
The quantification of net soil organic P mineralization rates is hampered by the potentially rapid sorption of released phosphate. Here, isotopic dilution approaches to assess gross and net organic P mineralization rates under steady-state conditions are reviewed, including different analytical and numerical solutions to assess P transformation rates based on incubation experiments with 32P- or 33P-labeled soils. Non-isotopic approaches are also commented on. Published isotopic dilution studies show that isotopically exchangeable P during incubation can partly or even predominantly (20–90%) result from biological and biochemical rather than physicochemical processes. The relative contribution of biological and biochemical processes tends to be lower in arable soils than under grassland and forests and is negatively related to the availability of inorganic P and positively to concentrations of soil organic carbon. Typical basal gross organic P mineralization rates range between 0.1 and 2.5 mg P kg−1 d−1, but rates up to 12.6 mg P kg−1 d−1 have been observed in grassland and forest soils. The further partitioning of gross organic P mineralization remains uncertain, but a dominance of microbial immobilization and remineralization is likely under most conditions, at least during the initial weeks of incubation. Over longer time periods, the relative importance of mineralization of non-living soil organic P increases, with the contribution of extracellular hydrolysis remaining to be elucidated. This requires other approaches than enzyme activity assays, since measurements of phosphomonoesterase activity in soil render organic P mineralization rates that are one to two orders of magnitude greater than those determined by isotopic dilution. The numerical modeling approach will enable assessment of soil P transformation rates under non-steady-state conditions, where P fluxes are likely to be greater than under steady-state conditions. Ultimately, an improved understanding of the biological and biochemical processes in soil P dynamics may help to improve P management in agroecosystems.  相似文献   

19.
Short-term competition between soil microbes and seedlings of Scots pine (Pinus sylvestris L.), Norway spruce (Picea abies (L.) Karst.) and silver birch (Betula pendula Roth) for N was assessed in a pot study using (15NH4)2SO4 as a tracer. Seedlings were grown in organic and mineral soil, collected from a podsol soil; 3.18 mg (15NH4)2SO4 per pot were injected into the soil, corresponding to 4 µg 15N g-1 d.m. (dry matter) mineral soil and 17 µg 15N g-1 d.m. organic soil. The amounts of N and 15N in the seedlings and in microbial biomass derived from fumigation-extraction were measured 48 h after addition of 15N. In the mineral soil, 19–30% of the added 15N was found in the plants and 14–20% in the microbial biomass. There were no statistically significant differences between the tree species. In the organic soil, 74% of the added 15N was recovered in the microbial biomass in birch soil, compared to 26% and 17% in pine and spruce soils, respectively. Correspondingly, about 70% of the 15N was recovered in pine and spruce seedlings, and only 23% in birch seedlings. In conclusion, plants generally competed more successfully for added 15NH4 + than soil microbes did. An exception was birch growing in organic soil, where the greater amount of available C from birch root exudates perhaps enabled micro-organisms to utilise more N.  相似文献   

20.
Background, aim, and scope  Hoop pine (Araucaria cunninghamii) is a nitrogen (N) demanding indigenous Australia softwood species with plantations in Southeast Queensland, Australia. Soil fertility has declined with increasing rotations and comparison study of N cycling between hoop pine plantations, and adjacent native forest (NF) is required to develop effective forest management for enhancing sustainable forest production and promoting environmental benefits. Field in situ mineral 15N transformations in these two forest ecosystems have not been studied. Hence, the present study was to compare the differences in soil nutrients, N transformations, 15N fluxes, and fate between the hoop pine plantation and the adjacent native forest. Materials and methods  The study sites were in Yarraman State Forest (26°52′ S, 151°51′ E), Southeastern Queensland, Australia. The in situ core incubation method was used in the field experiments. Mineral N was determined using a LACHAT Quickchem Automated Ion Analyzer. 15N were performed using an isotope ratio mass spectrometer with a Eurovector elemental analyzer. All statistical tests were carried out by the SPSS 11.0 for Windows statistical software package. Results  Soil total C and N were significantly higher in the NF than in the 53-year-old hoop pine plantation. Concentrations of NO3 – were significantly higher in the NF soil than in the plantation soil. The plantation soil had significantly higher 15N and 13C natural abundances than the NF soil. The NF soil had significantly lower C/N ratios than the plantation soil. NO3 ––N was dominated in mineral N pools in both NF and plantation soils, accounting for 91.6% and 70.3% of the total mineral N pools, respectively. Rates of net nitrification and net N mineralization were, respectively, four and three times higher in the NF soil than in the plantation soil. The 15NO3 ––N and mineral 15N were significantly higher in the NF soil than in the plantation soil. Significant difference in 15NH4 +–N was found in the NF soil before and after the incubation. Discussion  The NF soil had significantly higher NO3 ––N, mineral N, total N and C but lower δ15N, δ13C, and C/N ratios than the plantation soil. Moreover, the rates of soil net N mineralization and nitrification were significantly higher, but ammonification rate was lower in the NF than in the plantation. The NF soil had many more dynamic N transformations than the plantation soil due to the combination of multiple species and layers and, thus, stimulation of microbial activity and alteration of C and N pool sizes in favor of the N transformations by soil microbes. The net rate of N and 15N transformation demonstrated differences in N dynamic related to the variation in tree species between the two ecosystems. Conclusions  The change of land use and trees species had significant impacts on soil nutrients and N cycling processes. The plantation had larger losses of N than the NF. The NO3 ––N and 15NO3 ––N dominated in the mineral N and 15N pools in both forest ecosystems. Recommendations and perspectives  Native forest soil had strong N dynamic compared with the plantation soil. Composition of multiple tree species with different ecological niches in the plantation could promote the soil ecosystem sustainability. The 15N isotope dilution technique in the field can be quite useful for studying in situ mineral 15N transformations and fate to further understand actual N dynamics in natural forest soils.  相似文献   

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