Kinetic Parameters of Gross N Mineralization of Peat Soils as Related to the Composition of Soil Organic Matter

Peat land has been considered as an alternative type of land for agricultural development especially in the tropics. In the present study, the N-supplying capacity, one of the most important soil properties in terms of crop production, of peat soils was examined. Ten peat soil samples were collected from Indonesia, Malaysia, and Japan. Gross N mineralization in the soil samples was estimated using a zero-order model, and kinetic parameters of mineralization were determined using a simple type model. Soil organic matter composition was investigated using ¹³C CPMAS NMR. Mineralization potential ( N ₀), apparent activation energy ( E _a), and mineralization rate constant ( k ) ranged between 571–2,445 mg kg⁻¹, 281–8,181 J mol⁻¹, and 0.009–0.020 d⁻¹, respectively. Although none of the parameters showed a significant correlation with the soil C/N ratio, a negative correlation was observed between the k value and the ratio of the proportion of alkyl C in total C to that of O -alkyl C estimated by ¹³C CPMAS NMR. The latter suggested that the k values were higher in the peat soils relatively rich in readily decomposable organic matter including carbohydrates.     

用δ~(13)C法研究黑土添加有机物料后有机碳的变化规律

通过室内短期培养实验,利用δ13C的方法研究了外源有机物料分解过程中黑土有机碳的变化规律。结果表明:黑土中添加有机物料后,土壤有机碳的数量明显增加。在有机物料分解过程中,随着培养时间的延长,土壤有机碳的总量在逐渐下降,总的变化趋势是先快后慢,渐趋平缓,到培养结束(30天),有机物料在土壤中净残留率小于50%。黑土有机碳的δ13C值受进入土壤中有机物料的种类所影响,从数量上土壤有机碳的δ13C值可以反映土壤中不同来源有机碳的变化。在小麦秸秆分解过程中,新进入黑土中的有机碳转化较快,而土壤中固有的有机碳转化较慢,添加有机物料可以增加土壤中有机碳的固定。     

A GC/MS method for the assessment of N and C incorporation into soil amino acid enantiomers

Identifying the transformation process of amino acid enantiomers was essential to probe into the fate, turnover and aging of soil nitrogen due to their important roles in the biogeochemical cycling. If this can be achieved by differentiating between the newly biosynthesized and the inherent compounds in soil, then the isotope tracer method can be considered most valid. We thereby developed a gas chromatography/mass spectrometry (GC/MS) method to trace the ¹⁵N or ¹³C isotope incorporation into soil amino acid enantiomers after being incubated with ¹⁵NH₄⁺ or U-¹³C-glucose substrates. The most significant fragments (F) as well as the related minor ions were monitored by the full scan mode and the isotope enrichment in amino acids was estimated by calculating the atom percentage excess (APE). ¹⁵NH₄⁺ incorporation was evaluated according to the relative abundance increase of m/z F+1 to F for neutral and acidic amino acids and F+2 to F (mass 439) for lysine. The assessment of ¹³C enrichment in soil amino acids was more complicated than that of ¹⁵N due to multi-carbon atoms in amino acid molecules. The abundance ratio increment of m/z F+n to F (n is the original skeleton carbon number in each fragment) indicated the direct conversion from the added glucose to amino acids, but the total isotope incorporation from the added ¹³C can only be calculated according to all target isotope fragments, i.e. the abundance ratio increment summation from m/z (Fa+1) through m/z (Fa+T) represented the total incorporation of the added ¹³C (Fa is the fragment containing all original skeleton carbons and T is the carbon number in the amino acid molecule). This method has a great advantage especially for the evaluation of high-abundance isotope enrichment in organic compounds compared with GC/C/IRMS. And in principle, this technique is also valid for amino acids besides enantiomers if stereoisomers are not concerned. Our assessment approach could shine a light on investigating the biochemical mechanism of microbial transformation of N and C in soils of terrestrial ecosystem.     

Linking Microbial Community Dynamics Associated with Rhizosphere Carbon Flow in a Biofuel Crop (Jatropha curcas L.)

Photosynthetically derived rhizodeposits are an important source of carbon (C) for microbes in root vicinity and can influence the microbial community dynamics. Pulse labeling of carbon dioxide (¹³CO₂) coupled with stable isotope probing techniques have potential to track recently fixed photosynthate into rhizosphere microbial taxa. Therefore, the present investigation assessed the microbial community change associated with the rhizosphere and bulk soil in Jatropha curcas L. (a biofuel crop) by combining phospholipid fatty acid (¹³C-PLFA) profiling using a stable isotope ¹³CO₂ labeling approach. The labeling (¹³C) took place after 45 days of germination, PLFAs were extracted from both soils (rhizosphere and bulk) after 1 and 20 days pulse labeling and analyzed by gas chromatography-isotope ratio mass spectrometry. There was no significant temporal effect on the PLFA profiles in the bulk soil, but significantly increased abundance of Gram positive (i15:0) and Gram negative (16:1ω7c and 16:1ω5c) biomarkers was observed in the rhizosphere soil from day 1 to day 20 after labeling. The Gram negative (16:1ω7c) decreased and fungal (18:2ω6,9c) increased significantly in rhizospheric soil compared to bulk soil after day 1 of labeling. Whereas, after 20 days of labeling, the Gram negative biomarker (16:1ω7c and 18:1ω7c) decreased and Gram positive (a15:0) increased significantly in rhizospheric soil compared to bulk soil. One day following labeling, i15:0, a15:0, i16:0, 16:1ω5c, 16:0, i17:0, a17:0, 18:2ω6,9c, 18:1ω9c, and 18:0 PLFAs were significantly more enriched in δ¹³C in the rhizosphere than in the bulk soil. Twenty days after labeling, 16:1ω5c (Gram negative) and 18:2ω6,9c (fungal) were significantly more enriched in δ¹³C in the rhizosphere than in the bulk soil. These results shows the effectives of PLFA coupled using the pulse chase labeling technique to examine the microbial community changes in response to recently fixed photosynthetic C flow in rhizodeposits.     

稳定13C同位素示踪技术在农田土壤碳循环和团聚体 固碳研究中的应用进展

农田土壤有机碳库是全球碳循环的重要组成部分,其积累和分解直接影响陆地生态系统碳贮藏与全球碳平衡。土壤团聚体是土壤结构的物质基础和土壤肥力的重要载体,也是土壤有机碳的固定场所。稳定~(13)C同位素示踪技术是研究土壤碳动态变化的有效手段,能够揭示新输入碳在土壤及团聚体中赋存状态、周转过程以及微生物的调节机制。本文主要归纳与阐述了稳定~(13)C同位素示踪技术在农田土壤有机碳循环及土壤团聚体固碳机理方面的研究进展,提出~(13)C同位素示踪技术在未来土壤碳循环和固碳机制方面的主要研究方向。     

Fate of humic acids isolated from natural humic substances

Composition of humic acids (HA) is a function of plant-derived inputs, degradation processes regulated by microorganisms, organo-mineral interactions and age. Characterization of different origin humic substances is important for evaluation of their contribution to stabile and labile carbon pool in the environment. The relative abundance of chemical components in HA isolated from soils, compost, commercial lignohumates, alginite, acadiane and lignite was studied with aim to quantify content of important biomarkers such as amino acid, lipids and polyphenols. HA were considered as a heterogeneous complex and high concentration of peptides, polyphenols and lipids was determined in acadian-HA to compare with soil-HA. Compost-HA contained much more amino acids to compare with soil-HA samples. Alginite-HA and lignite-HA were similar in biomarkers content to soil-HA. Fourier transform infrared spectroscopy confirmed that chemical composition and functional groups content differs with the origin, humification degree and the age of studied samples. Soil-HA are typically composed of a variety of ?OH, COOH?, C–O, C–H₂, (aliphatic and aromatic) groups, quinines, lignin fragments, polysaccharide, monosaccharide and proteins fragments, which are linked together by ?O?, ?NH?, ?H=, >C=O, metal ions and –S? groups. ¹³C NMR spectroscopy showed that aromatic carbon content was the highest in lignite-HA and soil-HA.     

Investigations on the radioactive contamination of crop plants as a result of H-bomb detonation (Part 2) Root and foliage uptake of “Bikini ash”

The Foliar Uptake by Squash Plant

The radioactive ash for experimental use, hereafter referred to as “Bikini ash”, was prepared by igniting the heavily contaminated substances on board No. 5 Fukuryu Maru at about 650°C, followed by sifting through a 100 mesh sieve. On ignition some parts of the fission products, particularly iodine, ruthenium and tellurium would have possibly been lost to the air.     

Leaf litter decomposition in a chaparral ecosystem, Southern California

Decomposition losses from leaves of three evergreen chaparral species, scrub oak (Quercus dumosa), ceanothus (Ceanothus crassifolius), and manzanita (Arctostaphylos glauca), were quantified over a 2-y field exposure using litterbags. Changes in ash-free dry mass, C, and N were monitored at 2- to 6-month intervals at four replicate sites composed of patches of these three chaparral species. Three proximate C fractions were extracted from fresh and decomposing litter samples: polar and non-polar extractives (EXT), acid-solubles (ACID), and acid-insolubles (KLIG). The chemical structure of fresh and decomposed litter was additionally characterized using high-resolution solid-state ¹³C NMR spectroscopy, while morphological properties were examined by scanning electron microscopy (SEM). After 2 y, the litters had lost between 20.7%±1.2 (Ceanothus) and 35.2%±6.8 (Quercus) of their original ash-free dry mass. The manzanita decomposed at a significantly faster rate than the other two litter types during the first few months of field exposure. Yet, after 2 y, mass loss was greater for the oak. Differences in decomposition rates could not be accounted for based on a single litter quality index. Fresh manzanita exhibited a significantly higher N content, which could explain its initially faster decay rate. Fresh oak litter, on the other hand, had a relatively high ACID and O-alkyl C (O-ALK) content, which may have been responsible for its decay pattern. Fresh ceanothus contained a relatively low KLIG content, yet it decomposed more slowly than the two other species. The solid-state ¹³C NMR spectra of the ceanothus litter had two peaks characteristic of proanthocyanidins, which likely contributed to the recalcitrance of this litter type. SEM revealed that ceanothus leaf surfaces were left nearly unchanged after field exposure. In comparison, the oak and manzanita leaf surfaces were pitted and covered by microbial growth to the point of being unrecognizable. Taken together, our results indicate that a combination of biological, physical and chemical factors need to be examined to clarify the different decomposition rates and patterns of these three chaparral species.     

长期施肥对潮土团聚体有机碳分子结构的影响

采取长期施用有机肥（CM）、一半化肥氮和一半有机肥氮（HCM）、化肥（NPK）和不施肥对照（CK）的土壤,用湿筛法分为大团聚体（2000~250 μm）、微团聚体（250~53 μm）和粉砂 黏粒组分（<53 μm）,利用固态13C-核磁共振技术分析了土壤和团聚体中有机质的分子结构特征。结果表明,随着团聚体粒径减小,烷基碳/烷氧碳比值逐渐提高,并与土壤C/N呈显著负相关（R2 = 0.421,p = 0.022）,表明随着团聚体粒径减小,有机质的分解程度不断增加。与对照土壤相比,长期施用有机肥（HCM和CM处理）提高了土壤中烷氧碳和羰基碳的相对含量,烷氧碳的增加主要是由于大团聚体中甲氧基和含氮烷基碳相对含量的增加,羰基碳则主要在大团聚体和微团聚体中积聚。施用化肥土壤提高了烷氧碳和烷基碳的相对含量,烷氧碳增加主要是由于大团聚体中甲氧基和含氮烷基碳以及微团聚体中含氧烷基碳相对含量的提高,烷基碳增加主要发生在大团聚体。有机肥和化肥处理土壤中芳基碳相对含量降低1.8%~4.6%,主要是大团聚体和微团聚体中芳基碳比例下降引起的。而在粉砂 黏粒组分中芳基碳和酚基碳均增加,烷基碳相对含量降低5.9%~7.1%,表明施肥更利于芳香碳在小粒径组分中积累,减弱烷基碳在小粒径组分中的积累。结果表明长期施用有机肥可通过大团聚体和微团聚体物理保护肥料带入的大量碳水化合物和有机酸从而提高土壤有机碳含量。     

抽穗后干旱复水对双季杂交晚稻产量形成和叶片δ13C及内源激素水平的影响

为探明生育后期干旱复水对双季杂交晚稻不同产量潜力品种产量的影响及其形成的生理机制,选择超级稻品种五丰优T025和对照品种金优207,于抽穗后进行干旱8d复水处理,分析了2个品种结实和产量、干旱前后倒二叶稳定碳同位素组成(δ13C)及内源激素含量的差异性。结果表明,干旱复水处理下2个品种水稻的结实率、千粒重及单株产量较对照(保持水层)表现出不同程度下降。其中,结实率五丰优T025和金优207分别下降12.07%和7.67%,千粒重下降5.23%和9.09%,单株产量下降13.54%和27.14%,差异均达显著或极显著水平,未发现产量补偿效应。抽穗后干旱处理下倒二叶δ13C值,五丰优T025大幅上升,复水后呈现出先下降,至第6天又开始上升的特点,金优207则大幅下降,复水后呈现先上升后下降再上升的特点,五丰优T025较金优207干旱复水处理与对照之间的差距更大。总体上,对照条件下,抽穗至其后20d,随生育推进,2个品种倒二叶内源ABA和GA₃含量呈上升而IAA含量则下降趋势,ZR表现出先上升再下降特点。干旱处理下2个品种表现为ABA含量上升,复水后呈先下降后上升特点,五丰优T025较金优207处理与对照之间差距更大;干旱复水处理条件下:2个品种IAA含量均下降,五丰优T025处理与对照间的差距明显小于金优207;五丰优T025 GA₃含量表现出先上升后下降再上升,金优207表现出干旱处理结束日急剧下降至最低点,复水后缓慢上升特点;2个品种ZR含量呈现出先上升至最高值再下降特点,五丰优T025较金优207处理与对照之间差距更小。抽穗后干旱处理将启动稻株体内抗衰老机制,复水后将在一定程度一定时间内激活稻株体内生长促进因子并抑制生长抑制因子,但其效果十分有限。