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51.
Christiane Kramer 《Soil biology & biochemistry》2006,38(11):3267-3278
In this study we used compound specific 13C and 14C isotopic signatures to determine the degree to which recent plant material and older soil organic matter (SOM) served as carbon substrates for microorganisms in soils. We determined the degree to which plant-derived carbon was used as a substrate by comparison of the 13C content of microbial phospholipid fatty acids (PLFA) from soils of two sites that had undergone a vegetation change from C3 to C4 plants in the past 20-30 years. The importance of much older SOM as a substrate was determined by comparison of the radiocarbon content of PLFA from soils of two sites that had different 14C concentrations of SOM.The 13C shift in PLFA from the two sites that had experienced different vegetation history indicated that 40-90% of the PLFA carbon had been fixed since the vegetation change took place. Thus PLFA were more enriched in 13C from the new C4 vegetation than it was observed for bulk SOM indicating recent plant material as preferentially used substrate for soil microorganisms. The largest 13C shift of PLFA was observed in the soil that had high 14C concentrations of bulk SOM. These results reinforce that organic carbon in this soil for the most part cycles rapidly. The degree to which SOM is incorporated into microbial PLFA was determined by the difference in 14C concentration of PLFA derived from two soils one with high 14C concentrations of bulk SOM and one with low. These results showed that 0-40% of SOM carbon is used as substrate for soil microorganisms. Furthermore a different substrate usage was identified for different microorganisms. Gram-negative bacteria were found to prefer recent plant material as microbial carbon source while Gram-positive bacteria use substantial amounts of SOM carbon. This was indicated by 13C as well as 14C signatures of their PLFA. Our results find evidence to support ‘priming’ in that PLFA indicative of Gram-negative bacteria associated with roots contain both plant- and SOM-derived C. Most interestingly, we find PLFA indicative of archeobacteria (methanothrophs) that may indicate the use of other carbon sources than plant material and SOM to a substantial amount suggesting that inert or slow carbon pools are not essential to explain carbon dynamics in soil. 相似文献
52.
53.
J. Lehmann J. Lilienfein K. Rebel S. do Carmo Lima W. Wilcke 《Soil Use and Management》2004,20(2):163-172
Abstract. Nitrogen (N) loss by leaching poses great challenges for N availability to crops as well as nitrate pollution of groundwater. Few studies address this issue with respect to the role of the subsoil in the deep and highly weathered savanna soils of the tropics, which exhibit different adsorption and drainage patterns to soils in temperate environments. In an Anionic Acrustox of the Brazilian savanna, the Cerrado, dynamics and budgets of applied N were studied in organic and inorganic soil pools of two maize (Zea mays L.) – soybean (Glycine max (L.) Merr.) rotations using 15N tracing. Labelled ammonium sulphate was applied at 10 kg N ha?1 (with 10 atom%15N excess) to both maize and soybean at the beginning of the cropping season. Amounts and isotopic composition of N were determined in above‐ground biomass, soil, adsorbed mineral N, and in soil solution at 0.15, 0.3, 0.8, 1.2 and 2 m depths using suction lysimeters throughout one cropping season. The applied ammonium was rapidly nitrified or immobilized in soil organic matter, and recovery of applied ammonium in soil 2 weeks after application was negligible. Large amounts of nitrate were adsorbed in the subsoil (150–300 kg NO3?‐N ha?1 per 2 m) matching total N uptake by the crops (130–400 kg N ha?1). Throughout one cropping season, more applied N (49–77%; determined by 15N tracers) was immobilized in soil organic matter than was present as adsorbed nitrate (2–3%). Most of the applied N (71–96% of 15N recovery) was found in the subsoil at 0.15–2 m depth. This coincided with an increase with depth of dissolved organic N as a proportion of total dissolved N (39–63%). Hydrophilic organic N was the dominant fraction of dissolved organic N and was, together with nitrate, the most important carrier for applied N. Most of this N (>80%) was leached from the topsoil (0–0.15 m) during the first 30 days after application. Subsoil N retention as both adsorbed inorganic N, and especially soil organic N, was found to be of great importance in determining N losses, soil N depletion and the potential of nitrate contamination of groundwater. 相似文献
54.
青藏高原中部土壤水中稳定同位素变化 总被引:29,自引:0,他引:29
根据 1 998年夏季测得的青藏高原中部那曲地区降水和土壤水中稳定同位素 ,分析了不同层位土壤剖面中稳定同位素的变化规律及与水分迁移的关系。研究结果发现 ,土壤表层水中δ1 8O受降水中δ1 8O的直接影响 ,并且与降水中δ1 8O有相同的变化趋势 ,而地下水中δ1 8O受降水中δ1 8O的直接影响不明显 ,变化幅度很小 ,表明地下水并非直接来源于当年夏季的降水 ,可能代表了多年降水的平均状态。不同土壤剖面水中δ1 8O的变化反映了降水向地下逐渐渗浸的过程。表层土壤水中δ1 8O受降水的影响最为明显 ,而向下土壤水中δ1 8O受地下水δ1 8O的影响增强 ,显示出地下水在土壤水分活动中起着活跃的作用。 相似文献
55.
56.
田间小区试验研究了不同种植模式下苜蓿的共生固氮贡献,并利用~(15)N同位素示踪技术评估了苜蓿的%Ndfa和Ndfa,以及与之混作生长的牛尾草植株中来自苜蓿固氮产物的转移量。研究表明,豆科与禾本科牧草混作对发挥草地的优势有一定影响,混作条播在干草产量、全氮产量、%Ndfa和Ndfa等方面均优于间作与混作撒播模式,且高于单作苜蓿与牛尾草的平均值。用~(15)N同位素稀释法与~(15)N天然丰度法评估苜蓿的%Ndfa与Ndfa值时,无明显差异(P<0.05),前者还能准确测出混种牛尾革植株中的固氮产物转移量,后者则大大低估,甚至不能测出固氮产物转移。 相似文献
57.
通过温室盆栽试验 ,分析和探讨了三个水平的土壤水分条件对分蘖期和成熟期收获的旱稻(OryzasativaL .)生物量累积、水分利用率 (WUE)、植株不同部位的碳同位素识别值 (CID)的影响 ,并了解了它们之间的相互关系。水分条件包括 :饱和含水量 (W1 )、饱和含水量的 70 %(W2 )、饱和含水量的 4 0 %(W3)。结果表明当土壤水分条件从W1降低到W2时 ,分蘖期收获的生物量降低 4 5 %左右 ,成熟期收获的生物量降低 1 6 %~ 1 9%;而当从W1降低到W3时 ,分蘖期收获的生物量降低 73%左右 ,成熟期收获的生物量降低 5 5 %~ 5 7%。然而 ,根据地上部干重计算而来的WUE(WUE 地上部 )和根据全株干重计算而来的WUE(WUE 全株 )则随土壤含水量的降低而增加 ,其增幅在分蘖期为 0 .0 7~ 0 .2 8gkg-1 ,在成熟期为 0 .0 7~ 0 .4 5gkg-1 。植株的CID值变幅为 1 7.0~ 2 0 .6 ,但植株不同部位间差别显著 ,分蘖期收获的样品CID值从小到大的顺序为 :根 <最近完全伸展叶 <叶芽 <茎秆 ;而成熟期收获的样品CID值从小到大的顺序为 :籽粒 <根 <茎秆 <旗叶。随着土壤含水量的降低 ,植株所有部位的CID值亦显著减小。叶部的CID值与WUE 地上部(和WUE 全株 )之间呈一致的负相关关系。 相似文献
58.
Soil physical structure causes differential accessibility of soil organic carbon (SOC) to decomposer organisms and is an important determinant of SOC storage and turnover. Techniques for physical fractionation of soil organic matter in conjunction with isotopic analyses (δ13C, δ15N) of those soil fractions have been used previously to (a) determine where organic C is stored relative to aggregate structure, (b) identify sources of SOC, (c) quantify turnover rates of SOC in specific soil fractions, and (d) evaluate organic matter quality. We used these two complementary approaches to characterize soil C storage and dynamics in the Rio Grande Plains of southern Texas where C3 trees/shrubs (δ13C=−27‰) have largely replaced C4 grasslands (δ13C=−14‰) over the past 100-200 years. Using a chronosequence approach, soils were collected from remnant grasslands (Time 0) and from woody plant stands ranging in age from 10 to 130 years. We separated soil organic matter into specific size/density fractions and determined their C and N concentrations and natural δ13C and δ15N values. Mean residence times (MRTs) of soil fractions were calculated based on changes in their δ13C with time after woody encroachment. The shortest MRTs (average=30 years) were associated with all particulate organic matter (POM) fractions not protected within aggregates. Fine POM (53-250 μm) within macro- and microaggregates was relatively more protected from decay, with an average MRT of 60 years. All silt+clay fractions had the longest MRTs (average=360 years) regardless of whether they were found inside or outside of aggregate structure. δ15N values of soil physical fractions were positively correlated with MRTs of the same fractions, suggesting that higher δ15N values reflect an increased degree of humification. Increased soil C and N pools in wooded areas were due to both the retention of older C4-derived organic matter by protection within microaggregates and association with silt+clay, and the accumulation of new C3-derived organic matter in macroaggregates and POM fractions. 相似文献
59.
Summary We studied the effect of three successive cuttings on N uptake and fixation and N distribution in Leucaena leucocephala. Two isolines, uninoculated or inoculated with three different Rhizobium strains, were grown for 36 weeks and cut every 12 weeks. The soil was labelled with 50 ppm KNO3 enriched with 10 atom % 15N excess soon after the first cutting. Except for the atom % 15N excess in branches of K28 at the second cutting, both the L. leucocephala isolines showed similar patterns of total N, fixed N2, and N from fertilizer distribution in different parts of the plant at each cutting. The Rhizobium strain did not influence the partitioning of 15N among the different plant parts. Significant differences in 15N enrichment occurred in different parts. Live nodules of both isolines showed the lowest atom % 15N excess values (0.087), followed by leaves (0.492), branches (0.552), stems (0.591), and roots (0.857). The roots contained about 60% of the total plant N and about 70% of the total N derived from fertilizer over the successive cuttings. The total N2 fixed in the roots was about 60% of that fixed in the whole plant, while the shoots contained only 20% of the fixed N2. We conclude that N reserves in roots and nodules constitute another N source that must be taken into account when estimating fixed N2 or the N balance after pruning or cutting plants. 15N enrichment declined up to about fivefold in the reference and the N2-fixing plants over 24 weeks following the 15N application. The proportion and the amounts of N derived from fertilizer decreased, while the amount derived from N2 fixation increased with time although its proportion remained constant. 相似文献
60.
Paul Dijkstra Ayaka Ishizu Stephen C. Hart Egbert Schwartz Bruce A. Hungate 《Soil biology & biochemistry》2006,38(11):3257-3266
Stable isotope analysis is a powerful tool in the study of soil organic matter formation. It is often observed that more decomposed soil organic matter is 13C, and especially 15N-enriched relative to fresh litter and recent organic matter. We investigated whether this shift in isotope composition relates to the isotope composition of the microbial biomass, an important source for soil organic matter. We developed a new approach to determine the natural abundance C and N isotope composition of the microbial biomass across a broad range of soil types, vegetation, and climates. We found consistently that the soil microbial biomass was 15N-enriched relative to the total (3.2 ‰) and extractable N pools (3.7 ‰), and 13C-enriched relative to the extractable C pool (2.5 ‰). The microbial biomass was also 13C-enriched relative to total C for soils that exhibited a C3-plant signature (1.6 ‰), but 13C-depleted for soils with a C4 signature (−1.1 ‰). The latter was probably associated with an increase of annual C3 forbs in C4 grasslands after an extreme drought. These findings are in agreement with the proposed contribution of microbial products to the stabilized soil organic matter and may help explain the shift in isotope composition during soil organic matter formation. 相似文献