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1.
While it is well known that soil moisture directly affects microbial activity and soil organic matter (SOM) decomposition, it is unclear if the presence of plants alters these effects through rhizosphere processes. We studied soil moisture effects on SOM decomposition with and without sunflower and soybean. Plants were grown in two different soil types with soil moisture contents of 45% and 85% of field capacity in a greenhouse experiment. We continuously labeled plants with depleted 13C, which allowed us to separate plant-derived CO2-C from original soil-derived CO2-C in soil respiration measurements. We observed an overall increase in soil-derived CO2-C efflux in the presence of plants (priming effect) in both soils. On average a greater priming effect was found in the high soil moisture treatment (up to 76% increase in soil-derived CO2-C compared to control) than in the low soil moisture treatment (up to 52% increase). Greater plant-derived CO2-C and plant biomass in the high soil moisture treatment contributed to greater priming effects, but priming effects remained significantly higher in the high moisture treatment than in the low moisture treatment after correcting for the effects of plant-derived CO2-C and plant biomass. The response to soil moisture particularly occurred in the sandy loam soil by the end of the experiment. Possibly, production of root exudates increased with increased soil moisture content. Root exudation of labile C may also have become more effective in stimulating microbial decomposition in the higher soil moisture treatment and sandy loam soil. Our results indicate that moisture conditions significantly modulate rhizosphere effects on SOM decomposition.  相似文献   

2.
A deeper understanding of the contribution of carbon (C) released by plant roots (rhizodeposition) to soil organic matter (SOM) can help to increase our knowledge of global C-cycling. These insights can eventually lead to sustainable management of SOM especially in agricultural systems. This study was conducted to determine the fate of 13C labelled rhizodeposit-C of maize and wheat plants. They were grown in a greenhouse in permeable nylon bags filled with upper soil material from two agricultural soils of the same location, but with different crop yields. The bags were placed into pots, which were also filled with soil surrounding the bags. Soil inside the bags was considered as rhizosphere soil, wheras the one outside the bags represented bulk soil. The contributions of rhizodeposits to water extractable organic carbon (WEOC), microbial biomass-C (MB-C), CO2-C evolution, and total organic carbon (Corg) were investigated during a 7-week growing period. The WEOC, MB-C, CO2-C, Corg contents and the respective δ13C values were determined regularly, and a newly developed method for determining δ13C values in soil extracts was applied.In both soils, regardless of crop yield potential, significant incorporation of rhizodeposition-derived C was observed in the MB-C, CO2-C, and Corg pool, but not in the WEOC. The pattern of C incorporation into the different pools was the same for both soils with both plants, and rhizodeposit-derived C was recovered in the order MB-C<Corg<CO2-C. This showed that rhizodeposits were mainly respired, but since Corg was the second largest pool of the overall balances, they were also stabilized in the soils at least in the short term. It is suggested that the increased SOM mineralization observed in this study (positive priming effects) was probably induced by C exchange processes between the soil matrix and soluble rhizodeposits. Moreover, soluble rhizodeposit-C was detected in MB-C and CO2-C evolved outside the direct root zone, showing the availability of these C-components in the bulk soil.  相似文献   

3.
Sources of CO2 efflux from soil and review of partitioning methods   总被引：7，自引：0，他引：7  
Five main biogenic sources of CO2 efflux from soils have been distinguished and described according to their turnover rates and the mean residence time of carbon. They are root respiration, rhizomicrobial respiration, decomposition of plant residues, the priming effect induced by root exudation or by addition of plant residues, and basal respiration by microbial decomposition of soil organic matter (SOM). These sources can be grouped in several combinations to summarize CO2 efflux from the soil including: root-derived CO2, plant-derived CO2, SOM-derived CO2, rhizosphere respiration, heterotrophic microbial respiration (respiration by heterotrophs), and respiration by autotrophs. These distinctions are important because without separation of SOM-derived CO2 from plant-derived CO2, measurements of total soil respiration have very limited value for evaluation of the soil as a source or sink of atmospheric CO2 and for interpreting the sources of CO2 and the fate of carbon within soils and ecosystems. Additionally, the processes linked to the five sources of CO2 efflux from soil have various responses to environmental variables and consequently to global warming. This review describes the basic principles and assumptions of the following methods which allow SOM-derived and root-derived CO2 efflux to be separated under laboratory and field conditions: root exclusion techniques, shading and clipping, tree girdling, regression, component integration, excised roots and insitu root respiration; continuous and pulse labeling, 13C natural abundance and FACE, and radiocarbon dating and bomb-14C. A short sections cover the separation of the respiration of autotrophs and that of heterotrophs, i.e. the separation of actual root respiration from microbial respiration, as well as methods allowing the amount of CO2 evolved by decomposition of plant residues and by priming effects to be estimated. All these methods have been evaluated according to their inherent disturbance of the ecosystem and C fluxes, and their versatility under various conditions. The shortfalls of existing approaches and the need for further development and standardization of methods are highlighted.  相似文献   

4.
Understanding soil organic matter (SOM) decomposition and its interaction with rhizosphere processes is a crucial topic in soil biology and ecology. Using a natural 13C tracer method to separately measure SOM-derived CO2 from root-derived CO2, this study aims to connect the level of rhizosphere-dependent SOM decomposition with the C and N balance of the whole plant–soil system, and to mechanistically link the rhizosphere priming effect to soil microbial turnover and evapotranspiration. Results indicated that the magnitude of the rhizosphere priming effect on SOM decomposition varied widely, from zero to more than 380% of the unplanted control, and was largely influenced by plant species and phenology. Balancing the extra soil C loss from the strong rhizosphere priming effect in the planted treatments with C inputs from rhizodeposits and root biomass, the whole plant–soil system remained with a net carbon gain at the end of the experiment. The increased soil microbial biomass turnover rate and the enhanced evapotranspiration rate in the planted treatments had clear positive relationships with the level of the rhizosphere priming effect. The rhizosphere enhancement of soil carbon mineralization in the planted treatments did not result in a proportional increase in net N mineralization, suggesting a possible de-coupling of C cycling with N cycling in the rhizosphere.  相似文献   

5.
Elevated CO2 may increase nutrient availability in the rhizosphere by stimulating N release from recalcitrant soil organic matter (SOM) pools through enhanced rhizodeposition. We aimed to elucidate how CO2-induced increases in rhizodeposition affect N release from recalcitrant SOM, and how wild versus cultivated genotypes of wheat mediated differential responses in soil N cycling under elevated CO2. To quantify root-derived soil carbon (C) input and release of N from stable SOM pools, plants were grown for 1 month in microcosms, exposed to 13C labeling at ambient (392 μmol mol−1) and elevated (792 μmol mol−1) CO2 concentrations, in soil containing 15N predominantly incorporated into recalcitrant SOM pools. Decomposition of stable soil C increased by 43%, root-derived soil C increased by 59%, and microbial-13C was enhanced by 50% under elevated compared to ambient CO2. Concurrently, plant 15N uptake increased (+7%) under elevated CO2 while 15N contents in the microbial biomass and mineral N pool decreased. Wild genotypes allocated more C to their roots, while cultivated genotypes allocated more C to their shoots under ambient and elevated CO2. This led to increased stable C decomposition, but not to increased N acquisition for the wild genotypes. Data suggest that increased rhizodeposition under elevated CO2 can stimulate mineralization of N from recalcitrant SOM pools and that contrasting C allocation patterns cannot fully explain plant mediated differential responses in soil N cycling to elevated CO2.  相似文献   

6.
The mechanisms and specific sources of priming effects, i.e. short term changes of soil organic matter (SOM) decomposition after substance addition, are still not fully understood. These uncertainties are partly method related, i.e. until now only two C sources in released CO2 could be identified. We used a novel approach separating three carbon (C) sources in CO2 efflux from soil. The approach is based on combination of different substances originated from C3 or C4 plants in different treatments and identical transformation of substances like C3 sugar (from sugar beet) and C4 sugar (from sugar cane). We investigated the influence of the addition of two substances having different microbial utilizability, i.e. slurry and sugar on the SOM or/and slurry decomposition in two grassland soils with different levels of Corg (2.3 vs. 5.1% C). Application of slurry to the soil slightly accelerated the SOM decomposition. Addition of sugar lead to changes of SOM and slurry decomposition clearly characterized by two phases: immediately after sugar addition, the microorganisms switched from the decomposition of hardly utilizable SOM to the decomposition of easily utilizable sugar. This first phase was very short (2-3 days), hence was frequently missed in other experiments. The second phase showed a slightly increased slurry and SOM decomposition (compared to the soil without sugar). The separation of three sources in CO2 efflux from grassland soils allowed us to conclude that the C will be utilized according to its utilizability: sugar>slurry>SOM. Additionally, decomposition of more inert C (here SOM) during the period of intensive sugar decomposition was strongly reduced (negative priming effect). We conclude that, priming effects involve a chain of mechanisms: (i) preferential substrate utilization, (ii) activation of microbial biomass by easily utilizable substrate (iii) subsequent increased utilization of following substrates according to their utilizability, and (iv) decline to initial state.  相似文献   

7.
A greenhouse experiment was conducted by growing oats (Avenasativa L.) in a continuously 13CO2 labeled atmosphere. The allocation of 13C-labeled photosynthates in plants, microbial biomass in rhizosphere and root-free soil, pools of soil organic C, and CO2 emissions were examined over the plant's life cycle. To isolate rhizosphere from root-free soil, plant seedlings were placed into bags made of nylon monofilament screen tissue (16 μm mesh) filled with soil. Two peaks of 13C in rhizosphere pools of microbial biomass and dissolved organic carbon (DOC), as well as in CO2 emissions at the earing and ripeness stages were revealed. These 13C maxima corresponded to: (i) the end of rapid root growth and (ii) beginning of root decomposition, respectively. The δ13C values of microbial biomass were higher than those of DOC and of soil organic matter (SOM). The microbial biomass C accounted for up to 56 and 39% of 13C recovered in the rhizosphere and root-free soil, respectively. Between 4 and 28% of 13C assimilated was recovered in the root-free soil. Depending on the phenological stage, the contribution of root-derived C to total CO2 emission from soil varied from 61 to 92% of total CO2 evolved, including 4-23% attributed to rhizomicrobial respiration. While 81-91% of C substrates used for microbial growth in the root-free soil and rhizosphere came from SOM, the remaining 9-19% of C substrates utilized by the microbial biomass was attributable to rhizodeposition. The use of continuous isotopic labelling and physical separation of root-free and rhizosphere soil, combined with natural 13C abundance were effective in gaining new insight on soil and rhizosphere C-cycling.  相似文献   

8.
A greenhouse rhizobox experiment was carried out to investigate the fate and turnover of 13C‐ and 15N‐labeled rhizodeposits within a rhizosphere gradient from 0–8 mm distance to the roots of wheat. Rhizosphere soil layers from 0–1, 1–2, 2–3, 3–4, 4–6, and 6–8 mm distance to separated roots were investigated in an incubation experiment (42 d, 15°C) for changes in total C and N and that derived from rhizodeposition in total soil, in soil microbial biomass, and in the 0.05 M K2SO4–extractable soil fraction. CO2‐C respiration in total and that derived from rhizodeposition were measured from the incubated rhizosphere soil samples. Rhizodeposition C was detected in rhizosphere soil up to 4–6 mm distance from the separated roots. Rhizodeposition N was only detected in the rhizosphere soils up to 3–4 mm distance from the roots. Microbial biomass C and N was increased with increasing proximity to the separated roots. Beside 13C and 15N derived from rhizodeposits, unlabeled soil C and N (native SOM) were incorporated into the growing microbial biomass towards the roots, indicating a distinct acceleration of soil organic matter (SOM) decomposition and N immobilization into the growing microbial biomass, even under the competition of plant growth. During the soil incubation, microbial biomass C and N decreased in all samples. Any decrease in microbial biomass C and N in the incubated rhizosphere soil layers is attributed mainly to a decrease of unlabeled (native) C and N, whereas the main portion of previously incorporated rhizodeposition C and N during the plant growth period remained immobilized in the microbial biomass during the incubation. Mineralization of native SOM C and N was enhanced within the entire investigated rhizosphere gradient. The results indicate complex interactions between substrate input derived from rhizodeposition, microbial growth, and accelerated C and N turnover, including the decomposition of native SOM (i.e., rhizosphere priming effects) at a high spatial resolution from the roots.  相似文献   

9.
Plant roots can increase microbial activity and soil organic matter (SOM) decomposition via rhizosphere priming effects. It is virtually unknown how differences in the priming effect among plant species and soil type affect N mineralization and plant uptake. In a greenhouse experiment, we tested whether priming effects caused by Fremont cottonwood (Populus fremontii) and Ponderosa pine (Pinus ponderosa) grown in three different soil types increased plant available N. We measured primed C as the difference in soil-derived CO2-C fluxes between planted and non-planted treatments. We calculated “excess plant available N” as the difference in plant available N (estimated from changes in soil inorganic N and plant N pools at the start and end of the experiment) between planted and non-planted treatments. Gross N mineralization at day 105 was significantly greater in the presence of plants across all treatments, while microbial N measured at the same time was not affected by plant presence. Gross N mineralization was significantly positively correlated to the rate of priming. Species effects on plant available N were not consistent among soil types. Plant available N in one soil type increased in the P. fremontii treatment but not in the P. ponderosa treatment, whereas in the other two soils, the effects of the two plant species were reversed. There was no relationship between the cumulative amount of primed C and excess plant available N during the first 107 days of the experiment when inorganic N was still abundant in all planted soils. However, during the second half of the experiment (days 108-398) when soil inorganic N in the planted treatments was depleted by plant N uptake, the cumulative amount of primed C was significantly positively correlated to excess plant available N. Primed C explained 78% of the variability in plant available N for five of the six plant-soil combinations. Excess plant available N could not be predicted from cumulative amount of primed C in one species-soil type combination. Possibly, greater microbial N immobilization due to large inputs of rhizodeposits with low N concentration may have reduced plant available N or we may have underestimated plant available N in this treatment because of N loss through root exudation and death. We conclude that soil N availability cannot be determined by soil properties alone, but that is strongly influenced by root-soil interactions.  相似文献   

10.
The phenomenon that rhizosphere processes significantly control soil organic matter (SOM) decomposition, also termed rhizosphere priming effect (RPE), is now increasingly recognized as significant as the effects of soil temperature and moisture on SOM decomposition. However, the exact mechanisms responsible for RPE remain largely unknown. Particularly, some reports have suggested that the quality of rhizodeposits may play a significant role in causing different levels of RPE among various plant species. However, direct evidence for the “rhizodeposit quality hypothesis” has been lacking. Here we tested the hypothesis by investigating RPE on soil carbon (C) and nitrogen (N) mineralization of two soybean (Glycine max L. Merr.) isolines differing only in their ability to form nodules and to fix N2, and thus differing in tissue N concentration and rhizodeposit quality. We used a continuous 13C-labeling method for measuring RPE on soil organic C decomposition, and employed an N-budgeting method for quantifying RPE on soil net N mineralization. We found that the rhizodeposits from nodulated soybean produced a stronger RPE (53% vs. 26%) on soil organic C decomposition than the rhizodeposits from non-nodulated soybean at the maturity stage when nodulated soybean had significantly higher plant tissue N concentration but similar plant biomass, while both soybean isolines produced a similar RPE (33–34%) at the vegetative stage when there was no difference in plant tissue N concentration or plant biomass. The levels of RPE on soil net N mineralization were similar between the two isolines, ranging from 25% at the vegetative stage to 38–46% at the maturity stage. Moreover, RPE on soil organic C decomposition was not linearly proportional to RPE on soil net N mineralization. These results indicate that higher rhizodeposit quality is one of the most likely causes to the higher RPE of the nodulated soybean compared to the non-nodulated soybean. Further investigations of rhizodeposit quality and quantity between the two soybean isolines are warranted to further test this rhizodeposit quality hypothesis.  相似文献   

11.
The presence of plants induces strong accelerations in soil organic matter (SOM) mineralization by stimulating soil microbial activity – a phenomenon known as the rhizosphere priming effect (RPE). The RPE could be induced by several mechanisms including root exudates, arbuscular mycorrhizal fungi (AMF) and root litter. However the contribution of each of these to rhizosphere priming is unknown due to the complexity involved in studying rhizospheric processes. In order to determine the role of each of these mechanisms, we incubated soils enclosed in nylon meshes that were permeable to exudates, or exudates & AMF or exudates, AMF and roots under three grassland plant species grown on sand. Plants were continuously labeled with 13C depleted CO2 that allowed distinguishing plant-derived CO2 from soil-derived CO2. We show that root exudation was the main way by which plants induced RPE (58–96% of total RPE) followed by root litter. AMF did not contribute to rhizosphere priming under the two species that were significantly colonized by them i.e. Poa trivialis and Trifolium repens. Root exudates and root litter differed with respect to their mechanism of inducing RPE. Exudates induced RPE without increasing microbial biomass whereas root litter increased microbial biomass and raised the RPE mediating saprophytic fungi. The RPE efficiency (RPE/unit plant-C assimilated into microbes) was 3–7 times higher for exudates than for root litter. This efficiency of exudates is explained by a microbial allocation of fresh carbon to mineralization activity rather than to growth. These results suggest that root exudation is the main way by which plants stimulated mineralization of soil organic matter. Moreover, the plants through their exudates not only provide energy to soil microorganisms but also seem to control the way the energy is used in order to maximize soil organic matter mineralization and drive their own nutrient supply.  相似文献   

12.
The impact of rising atmospheric carbon dioxide (CO2) may be mitigated, in part, by enhanced rates of net primary production and greater C storage in plant biomass and soil organic matter (SOM). However, C sequestration in forest soils may be offset by other environmental changes such as increasing tropospheric ozone (O3) or vary based on species-specific growth responses to elevated CO2. To understand how projected increases in atmospheric CO2 and O3 alter SOM formation, we used physical fractionation to characterize soil C and N at the Rhinelander Free Air CO2-O3 Enrichment (FACE) experiment. Tracer amounts of 15NH4+ were applied to the forest floor of Populus tremuloides, P. tremuloides-Betula papyrifera and P. tremuloides-Acer saccharum communities exposed to factorial CO2 and O3 treatments. The 15N tracer and strongly depleted 13C-CO2 were traced into SOM fractions over four years. Over time, C and N increased in coarse particulate organic matter (cPOM) and decreased in mineral-associated organic matter (MAOM) under elevated CO2 relative to ambient CO2. As main effects, neither CO2 nor O3 significantly altered 15N recovery in SOM. Elevated CO2 significantly increased new C in all SOM fractions, and significantly decreased old C in fine POM (fPOM) and MAOM over the duration of our study. Overall, our observations indicate that elevated CO2 has altered SOM cycling at this site to favor C and N accumulation in less stable pools, with more rapid turnover. Elevated O3 had the opposite effect, significantly reducing cPOM N by 15% and significantly increasing the C:N ratio by 7%. Our results demonstrate that CO2 can enhance SOM turnover, potentially limiting long-term C sequestration in terrestrial ecosystems; plant community composition is an important determinant of the magnitude of this response.  相似文献   

13.
The fate of carbon (C) in grassland soils is of particular interest since the vast majority in grassland ecosystems is stored below ground and respiratory C‐release from soils is a major component of the global C balance. The use of 13C‐depleted CO2 in a 10‐year free‐air carbon dioxide enrichment (FACE) experiment, gave a unique opportunity to study the turnover of the C sequestered during this experiment. Soil organic matter (SOM), soil air and plant material were analysed for δ13C and C contents in the last year of the FACE experiment (2002) and in the two following growing seasons. After 10 years of exposure to CO2 enrichment at 600 ppmv, no significant differences in SOM C content could be detected between fumigated and non‐fumigated plots. A 13C depletion of 3.4‰ was found in SOM (0–12 cm) of the fumigated soils in comparison with the control soils and a rapid decrease of this difference was observed after the end of fumigation. Within 2 years, 49% of the C in this SOM (0–12 cm) was exchanged with fresh C, with the limitation that this exchange cannot be further dissected into respiratory decay of old C and freshly sequestered new C. By analysing the mechanistic effects of a drought on the plant‐soil system it was shown that rhizosphere respiration is the dominant factor in soil respiration. Consideration of ecophysiological factors that drive plant activity is therefore important when soil respiration is to be investigated or modelled.  相似文献   

14.
利用~(13)C标记和自然丰度三源区分玉米根际CO_2释放   总被引：1，自引：1，他引：0  
石灰性土壤中,根际土壤释放的CO_2有三个来源,即根源呼吸、土壤有机碳(SOC)分解和土壤无机碳(SIC)溶解,三源区分土壤释放的CO_2是量化土壤碳平衡的前提。分别在玉米拔节期、抽穗期和灌浆期进行7 h的~(13)O_2脉冲标记,经过27 d示踪期后破坏性取样,测定~(13)标记与自然丰度处理中,玉米地上部、根系、土壤和土壤CO_2的碳含量和δ~(13)值,利用~(13)示踪并结合自然丰度法区分玉米土壤CO_2的来源。研究结果显示,随着玉米生长,根源呼吸对土壤CO_2的贡献呈降低趋势,从拔节期的66.7%降低至灌浆期的25.8%。整个玉米旺盛生育期内(从拔节期到生育期末),根源呼吸和土壤总碳释放对土壤CO_2具有同等贡献,SOC和SIC释放对土壤总碳释放的贡献率分别为30%和20%。玉米生长对土壤的碳输入(根系+根际沉积物)超过土壤总碳(SIC+SOC)的释放,总体表现为土壤碳汇。研究表明,SIC溶解对全球碳库稳定性和调节CO_2浓度的影响非常重要,若忽视石灰性土壤中SIC溶解,则会高估SOC的分解,进而影响SOC激发效应以及土壤碳平衡的评估。  相似文献   

15.
It is still unclear whether elevated CO2 increases plant root exudation and consequently affects the soil microbial biomass. The effects of elevated CO2 on the fate of the C and nitrogen (N) contained in old soil organic matter pools is also unclear. In this study the short and long-term effects of elevated CO2 on C and N pools and fluxes were assessed by growing isolated plants of ryegrass (Lolium perenne) in glasshouses at elevated and ambient atmospheric CO2 and using soil from the New Zealand FACE site that had >4 years exposure to CO2 enrichment. Using 14CO2 pulse labelling, the effects of elevated CO2 on C allocation within the plant-soil system were studied. Under elevated CO2 more root derived C was found in the soil and in the microbial biomass 48 h after labelling. The increased availability of substrate significantly stimulated soil microbial growth and acted as priming effect, enhancing native soil organic matter decomposition regardless of the mineral N supply. Despite indications of faster N cycling in soil under elevated CO2, N availability to plants stayed unchanged. Soil previously exposed to elevated CO2 exhibited a higher N cycling rate but again there was no effect on plant N uptake. With respect to the difficulties of extrapolating glasshouse experiment results to the field, we concluded that the accumulation of coarse organic matter observed in the field under elevated CO2 was probably not created by an imbalance between C and N but was likely to be due to more complex phenomena involving soil mesofauna and/or other nutrients limitations.  相似文献   

16.
C efflux from soils is a large component of the global C exchange between the biosphere and the atmosphere. However, our understanding of soil C efflux is complicated by the “rhizosphere priming effect,” in which the presence of live roots may accelerate or suppress the decomposition of soil organic C. Due to technical obstacles, the rhizosphere priming effect is under-studied, and we know little about rhizosphere priming in tree species. We measured the rates of soil-derived C mineralization in root-free soil and in soil planted with cottonwood (Populus fremontii) trees. Live cottonwood roots greatly accelerated (a rhizosphere priming effect) or suppressed (a negative rhizosphere priming effect) the mineralization of soil organic C, depending upon the time of the year. At its maximum, soil organic C was mineralized nine times faster in the presence of cottonwood roots than in the unplanted controls. Over the course of the experiment, approximately twice as much soil organic C was mineralized in pots planted with cottonwoods compared to unplanted control pots. Soil organic C mineralization rates in the unplanted controls were temperature-sensitive. In contrast, soil organic C mineralization in the cottonwood rhizosphere was unresponsive to seasonal temperature changes, due to the strength of the rhizosphere priming effect. The rhizosphere priming effect is of key importance to our understanding of soil C mineralization, because it means that the total soil respiration is not a simple additive function of soil-derived and plant-derived respiration.  相似文献   

17.
Subtropical recent alluvial soils are low in organic carbon (C). Thus, increasing organic C is a major challenge to sustain soil fertility. Biochar amendment could be an option as biochar is a C-rich pyrolyzed material, which is slowly decomposed in soil. We investigated C mineralization (CO2-C evolution) in two types of soils (recent and old alluvial soils) amended with two feedstocks (sugarcane bagasse and rice husk) (1%, weight/weight), as well as their biochars and aged biochars under a controlled environment (25 ±2 ℃) over 85 d. For the recent alluvial soil (charland soil), the highest absolute cumulative CO2-C evolution was observed in the sugarcane bagasse treatment (1 140 mg CO2-C kg-1 soil) followed by the rice husk treatment (1 090 mg CO2-C kg-1 soil); the lowest amount (150 mg CO2-C kg-1 soil) was observed in the aged rice husk biochar treatment. Similarly, for the old alluvial soil (farmland soil), the highest absolute cumulative CO2-C evolution (1 290 mg CO2-C kg-1 soil) was observed in the sugarcane bagasse treatment and then in the rice husk treatment (1 270 mg CO2-C kg-1 soil); the lowest amount (200 mg CO2-C kg-1 soil) was in the aged rice husk biochar treatment. Aged sugarcane bagasse and rice husk biochar treatments reduced absolute cumulative CO2-C evolution by 10% and 36%, respectively, compared with unamended recent alluvial soil, and by 10% and 18%, respectively, compared with unamended old alluvial soil. Both absolute and normalized C mineralization were similar between the sugarcane bagasse and rice husk treatments, between the biochar treatments, and between the aged biochar treatments. In both soils, the feedstock treatments resulted in the highest cumulative CO2-C evolution, followed by the biochar treatments and then the aged biochar treatments. The absolute and normalized CO2-C evolution and the mineralization rate constant of the stable C pool (Ks) were lower in the recent alluvial soil compared with those in the old alluvial soil. The biochars and aged biochars had a negative priming effect in both soils, but the effect was more prominent in the recent alluvial soil. These results would have good implications for improving organic matter content in organic C-poor alluvial soils.  相似文献   

18.
Elevated CO2 and defoliation effects on nitrogen (N) cycling in rangeland soils remain poorly understood. Here we tested whether effects of elevated CO2 (720 μl L−1) and defoliation (clipping to 2.5 cm height) on N cycling depended on soil N availability (addition of 1 vs. 11 g N m−2) in intact mesocosms extracted from a semiarid grassland. Mesocosms were kept inside growth chambers for one growing season, and the experiment was repeated the next year. We added 15N (1 g m−2) to all mesocosms at the start of the growing season. We measured total N and 15N in plant, soil inorganic, microbial and soil organic pools at different times of the growing season. We combined the plant, soil inorganic, and microbial N pools into one pool (PIM-N pool) to separate biotic + inorganic from abiotic N residing in soil organic matter (SOM). With the 15N measurements we were then able to calculate transfer rates of N from the active PIM-N pool into SOM (soil N immobilization) and vice versa (soil N mobilization) throughout the growing season. We observed significant interactive effects of elevated CO2 with N addition and defoliation with N addition on soil N mobilization and immobilization. However, no interactive effects were observed for net transfer rates. Net N transfer from the PIM-N pool into SOM increased under elevated CO2, but was unaffected by defoliation. Elevated CO2 and defoliation effects on the net transfer of N into SOM may not depend on soil N availability in semiarid grasslands, but may depend on the balance of root litter production affecting soil N immobilization and root exudation affecting soil N mobilization. We observed no interactive effects of elevated CO2 with defoliation. We conclude that elevated CO2, but not defoliation, may limit plant productivity in the long-term through increased soil N immobilization.  相似文献   

19.
Priming effect and C storage in semi-arid no-till spring crop rotations   总被引：2，自引：0，他引：2  
Adoption of less invasive management practices, such as no-till (NT) and continuous cropping, could reduce CO2 emissions from agricultural soils by retaining soil organic matter (SOM). We hypothesized that C storage increases as cropping intensity increases and tillage decreases. We also hypothesized that pulsed addition of C increases the mineralization of native SOM. We evaluated C storage at the 0- to 5-cm depth in soils from four crop rotations: winter wheat-fallow, spring wheat-chemical fallow, continuous hard red spring wheat, and spring wheat-spring barley on a Ritzville silt loam (Calcidic Haploxeroll). In two incubation studies using 14C-labeled wheat straw, we traced the decomposition of added residue as influenced by (1) cropping frequency, (2) tillage, and (3) pulsed additions of C. Differences in 14C mineralization did not exist among the four rotations at any time throughout the incubations. However, differences in total CO2 production between the continuous wheat rotations and the fallow rotations point to a priming of native SOM, the degree of which appears to be related to the relative contributions of fungi and bacteria to the decomposition of added residue. Addition of non-labeled wheat straw to select samples in the second incubation resulted in a flush of 14C-CO2 not seen in the controls. This priming effect suggests C inputs have a greater effect on mineralization of residual C compared to disturbance and endogenous metabolism appears to be the source of primed C, with priming becoming more pronounced as the fungal:bacterial ratio in the soil increases.  相似文献   

20.
A theoretical approach to the partitioning of carbon dioxide (CO2) efflux from soil with a C3 vegetation history planted with maize (Zea mays), a C4 plant, into three sources, root respiration (RR), rhizomicrobial respiration (RMR), and microbial soil organic matter (SOM) decomposition (SOMD), was examined. The δ13C values of SOM, roots, microbial biomass, and total CO2 efflux were measured during a 40-day growing period. A three-source isotopic mass balance based on the measured δ13C values and on assumptions made in other studies showed that RR, RMR, and SOMD amounted to 91%, 4%, and 5%, respectively. Two assumptions were thoroughly examined in a sensitivity analysis: the absence of 13C fractionation and the conformity of δ13C of microbial CO2 and that of microbial biomass. This approach strongly overestimated RR and underestimated RMR and microbial SOMD. CO2 efflux from unplanted soil was enriched in 13C by 2.0‰ compared to microbial biomass. The consideration of this 13C fractionation in the mass balance equation changed the proportions of RR and RMR by only 4% and did not affect SOMD. A calculated δ13C value of microbial CO2 by a mass balance equation including active and inactive parts of microbial biomass was used to adjust a hypothetical below-ground CO2 partitioning to the measured and literature data. The active microbial biomass in the rhizosphere amounted to 37% to achieve an appropriate ratio between RR and RMR compared to measured data. Therefore, the three-source partitioning approach failed due to a low active portion of microbial biomass, which is the main microbial CO2 source controlling the δ13C value of total microbial biomass. Since fumigation-extraction reflects total microbial biomass, its δ13C value was unsuitable to predict δ13C of released microbial CO2 after a C3-C4 vegetation change. The second adjustment to the CO2 partitioning results in the literature showed that at least 71% of the active microbial biomass utilizing maize rhizodeposits would be necessary to achieve that proportion between RR and RMR observed by other approaches based on 14C labelling. The method for partitioning total below-ground CO2 efflux into three sources using a natural 13C labelling technique failed due to the small proportion of active microbial biomass in the rhizosphere. This small active fraction led to a discrepancy between δ13C values of microbial biomass and of microbially respired CO2.  相似文献   

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