Chemical stabilization of soil organic nitrogen by phenolic lignin residues in anaerobic agroecosystems

This review summarizes independent reports of yield decreases in several agricultural systems that are associated with repeated cropping under wet or submerged soil conditions. Crop and soil data from most of these agroecosystems have led researchers to attribute yield decreases to a reduction in crop uptake of N mineralized from soil organic matter (SOM). These trends are most evident in several long-term field experiments on continuous lowland rice systems in the Philippines, but similar trends are evident in a continuous rice rotation in Arkansas, USA and with no-till cropping systems in North American regions with cool, wet climatic conditions in Spring. Soil analyses from some of these systems have found an accumulation of phenolic lignin compounds in SOM. Phenolic compounds covalently bind nitrogenous compounds into recalcitrant forms in laboratory conditions and occurrence of this chemical immobilization under field conditions would be consistent with field observations of reduced soil N supply. However, technological shortcomings have precluded its demonstration for naturally formed SOM. Through recent advances in nuclear magnetic resonance spectroscopy, agronomically significant quantities of lignin-bound N were found in a triple-cropped rice soil in the Philippines. A major research challenge is to demonstrate in the anaerobic agroecosystems that these lignin residues bind sufficient quantities of soil N to cause the observed yield decreases. A key objective will be to elucidate the cycling dynamics of lignin-bound N relative to the seasonal pattern of crop N demand. Anaerobic decomposition of crop residues may be the key feature of anaerobic cropping systems that promotes the accumulation of phenolic lignin residues and hence the covalent binding of soil N. Potential mitigation options include improved timing of applied N fertilizer, which has already been shown to reverse yield decreases in tropical rice, and aerobic decomposition of crop residues, which can be accomplished through field drainage or timing of tillage operations. Future research will evaluate whether aerobic decomposition promotes the formation of phenol-depleted SOM and greater in-season N mineralization, even when the soil is otherwise maintained under flooded conditions during the growing season.     

Displacement imaging in porous media using the line scan NMR technique

Displacement imaging is a recent, powerful NMR method with which distributions of displacements can be acquired of e.g. fluids within a porous medium. Both motion parallel and perpendicular to the flow direction may be observed within a time window of a few milliseconds to several seconds. By combining displacement imaging with the line scan technique, one-dimensionally resolved measurements with a high temporal resolution ( < 1 min) of the spatial dependency of motion can be obtained. Here we present displacement images of flow through two simple model systems for soil: an unconsolidated glass bead water system and a sintered glass bead filter. It is demonstrated that the combination of displacement imaging and spatial resolution along a line is important to access both bulk displacement and local displacements in relation to the local porosity.     

A comparison of two methods for the isolation of free and occluded particulate organic matter

Various methods exist for the isolation of particulate organic matter (POM), one of the soil‐organic‐matter (SOM) fractions reacting most sensitive on land‐use or soil‐management changes. A combination of density separation and ultrasonic treatment allows to isolate two types of POM: (1) free POM and (2) POM occluded in soil aggregates. POM fractions are closely linked to their biochemical function for the formation and stabilization of aggregates, therefore methods using different aggregate sizes may result in different POM fractions isolated. We evaluated two physical fractionation procedures to reveal whether they yield different POM fractions with respect to amount and composition, using grassland and arable soils with sandy‐loam to sandy–clay‐loam texture and thus low macroaggregate stability. Method I used air‐dried aggregates of <2.0 mm size and a low‐energy sonication for aggregate disruption, method II used field‐moist aggregates <6.3 mm and a high‐energy–sonication procedure for aggregate disruption. POM fractions were analyzed by elemental analysis (C, N) and CPMAS ¹³C‐NMR spectroscopy. With both methods, about similar proportions of the SOM are isolated as free or occluded POM, respectively. The free‐ and occluded‐POM fractions obtained with method I are also rather similar in C and N concentration and composition as shown by ¹³C‐NMR spectroscopy. Method II isolates a free‐ and occluded‐POM fraction with significantly different C and N concentrations. NMR spectra revealed significant differences in the chemical composition of both fractions from method II, with the occluded POM having lower amounts of O‐alkyl C and higher amounts of aryl C and alkyl C than the free POM. Due to the use of larger, field‐moist aggregates with minimized sample pretreatment, two distinctly different POM fractions are isolated with method II, likely to be more closely linked to their biochemical function for the formation and stabilization of aggregates. High‐energy sonication as in method II also disrupts small microaggregates <63 µm and releases fine intraaggregate POM. This fraction seems to be a significant component of occluded POM, that allows a differentiation between free and occluded POM in sandy soils with significant microaggregation. It can be concluded, that microaggregation in arable soils with sandy texture is responsible for the storage of a more degraded occluded POM, that conversely supports the stabilization of fine microaggregates.     

Saprotrophic fungi transform organic phosphorus from spruce needle litter

Fungal decomposition of and phosphorus transformation from spruce litter needles (Picea abies) were simulated in systems containing litter needles inoculated with individual saprotrophic fungal strains and their mixtures. Fungal strains of Setulipes androsaceus (L.) Antonín, Chalara longipes (Preus) Cooke, Ceuthospora pinastri (Fr.) Höhn., Mollisia minutella (Sacc.) Rehm, Scleroconidioma sphagnicola Tsuneda, Currah & Thormann and an unknown strain NK11 were used as representatives of autochthonous mycoflora. Systems were incubated for 5.5 months in laboratory conditions. Fungal colonization in systems and competition among strains were assessed using the reisolation of fungi from individual needles. After incubation, needles were extracted with NaOH and extracts were analysed using ³¹P nuclear magnetic resonance spectroscopy (NMR). Needle decomposition was determined based on the decrease in C:N ratio. Systems inoculated with the basidiomycete S. androsaceus revealed substantial decrease in C:N ratio (from 25.8 to 11.3) while the effect of ascomycetes on the C:N ratio was negligible. We suppose that tested strains of saprotrophic ascomycetes did not participate substantially in litter decomposition, but were directly involved in phosphorus transformation and together with S. androsaceus could transform orthophosphate monoesters and diesters from spruce litter needles into diphosphates, polyphosphates and phosphonates. These transformations seem to be typical for saprotrophic fungi involved in litter needle decomposition, although the proportion of individual phosphorus forms differed among studied fungal strains. Phosphonate presence in needles after fungal inoculation is of special interest because no previous investigation recorded phosphonate synthesis and accumulation by fungi. Our results confirmed that the ³¹P NMR spectroscopy is an excellent instrumental method for studying transformations of soil organic phosphorus during plant litter decomposition. We suggest that polyphosphate production by S. androsaceus may contribute to the phosphorus cycle in forest ecosystems because this fungus is a frequent litter colonizer that substantially participates in decomposition.     

土壤腐殖物质的固体13C核磁共振技术研究

土壤腐殖物质的组成和结构复杂,其中含有多种官能团,是土壤碳库中的重要组成部分.固态13C NMR是研究有机化合物结构的有效手段,特别对于不溶性HM,已成为其研究的重要技术方法.本文主要介绍了固体13C NMR在土壤腐殖物质中的应用概况,总结、归纳了土壤腐殖物质中不同官能团所对应的信号区间,对比分析了腐殖物质中不同组分的结构区别,讨论分析了固体13C NMR在土壤腐殖物质结构与形态研究中的应用,以期借助固体13C NMR更加深入地对腐殖物质整体结构进行研究,推进对腐殖物质形成、转化的探讨.     

Nanoscale in Wood,Nanowood and Wood—Inorganic Nanocomposites

In order to introduce nano science and technology(NST) into the research field of wood science and technology,and promote the research of wood science and wood-inorganic composites to nanoscale ,some new concepts,such as the nano space in wood,nano structure units of wood and nanowood are put forward in this paper based on the layer structure of wood cell wall and the pile-up model of its main components.Furthermore,the process of preparing nanowood is discussed,and wood-inorganic nanocomposites may be operated in three ways with wood (matrix) and inorganic filler phase in 0-2,0-3 or 2-3 dimensions respectively.The following results are obtained:(1) The nanoscale voids in wood indicate that wood has inherent space to accommodate nanosized materials,such as nanoparticles,nanotubes and nanosticks;(2) According to the size from top down,the nano structure units in wood can be classified as :nanolayers,nano CMF (cellulose microfibril) and matrixd,nano crystallite units and cellulose chain clusters,and these can theroretically from nanowood;(3) The preparation of wood-inorganic nanocomposites can be operated on 0-2,0-3 or 2-3 dimensions.     

Effects of ultrasound and high pressure argon on physico-chemical properties of white mushrooms (Agaricus bisporus) during postharvest storage

Effects of high pressure argon (H), ultrasound (U) and their combination treatments (UH) on physico-chemical characteristics of white mushrooms were studied during 9 d of postharvest storage at 4 °C. H treated samples exhibited the smallest weight loss and respiration rate compared to all other samples. Mass losses after 9 d of storage were 3.01%, 5.09%, 5.39% and 9.59% for H, UH, U and untreated mushrooms, respectively. Furthermore, U treated samples showed lower polyphenol oxidase activity (PPO, E.C. 1.14.18.1) during storage while UH treated samples showed a slight increase in antioxidant capacity during storage and also experienced reduced mass loss and respiration rate. In addition, treated samples were effective in retaining mushrooms colour changes compared to control. Physico-chemical properties of differently treated mushrooms (UH, H and U) stored at 4 °C were significantly different (p < 0.05) from control.     

Characterization of the bound residues of the fungicide cyprodinil formed in plant cell suspension cultures of wheat

The non-extractable residues of the fungicide cyprodinil formed in heterotrophic cell suspension cultures of wheat were studied by application of [2-pyrimidyl-14C] or [2-pyrimidyl-13C]cyprodinil. The main objective was to examine whether solid-state and liquid 13C NMR spectroscopy can be used to examine plant bound residues of pesticides. For 14C experiments, wheat suspensions grown on glucose as carbon source were treated with 10 mg litre(-1) of 14C-cyprodinil. After incubation for 12 days, 20% of applied 14C was detected as non-extractable residues. The cell debris were treated with 0.1 M HCl (reflux), 1.0 M HCl (reflux), buffer, or 2 M NaOH (50 degrees C); Bj?rkman lignin and acidolysis lignin fractions were also prepared from the debris. Radioactivity liberated and solubilized by these procedures was examined by thin-layer chromatography and high-performance liquid chromatography. The results showed that cyprodinil and primary metabolites contributed to the fungicide's bound residues. Most of the residues (12% of applied 14C) remained associated with polar or polymeric/oligomeric endogenous cell materials in a stable manner. For the study with 13C-cyprodinil, wheat suspensions were cultivated on 13C-depleted glucose for four growth cycles, resulting in maximum 13C depletion of the natural cell components to about 0.10%. During the fourth cycle, 13C-labelled cyprodinil was applied, and cells were incubated (12 days). Cell debris was prepared and examined by solid-state 13C NMR spectroscopy. Debris was then treated as described above in the 14C experiment. Solubilized fractions were analyzed by liquid 13C NMR spectroscopy. However, none of the 13C NMR spectra recorded gave utilizable or unambiguous results, and all exhibited large inconsistencies, especially concerning the data from the conventional 14C experiment.     

六甲基六元瓜环与紫精衍生物作用体系及其除草活性研究

以紫精衍生物为研究对象,利用核磁共振技术、紫外吸收光谱和循环伏安法等方法,发现六甲基六元瓜环包结了紫精衍生物的烷基部分,形成2∶1比例的哑铃型包结配合物.结果表明,随着紫精衍生物烷基链的增长,紫精衍生物对杂草的除草活性依次减弱,且六甲基六元瓜环可增强紫精衍生物的除草活性.     

Serum chloramphenicol levels and the intramuscular bioavailability of several parenteral formulations of chloramphenicol in ruminants

Summary

Serum chloramphenicol concentrations were determined by microbiological and chemical assay methods in cows, ewes, and goats treated parenterally with seven different veterinary parenteral chloramphenicol products, including the water soluble sodium succinate ester of chloramphenicol and solutions of 20%, 25% and 50% of chloramphenicol base in various organic solvents. Serum drug concentrations were analyzed for the effect of product formulation differences, dosage, whether the drug was administered i.m. at a single body site or to two sites, and the method of assay, on the absorption from the injection site, peak drug levels, and the persistence in serum of effective concentrations of the drug i.e. 5 to 10 ug / ml. Although differences were observed among the 6 products containing chloramphenicol base in respect to absorption rate and peak serum drug levels, and although these differences significantly influenced the persistence of microbiologically‐active serum drug concentrations at the level of ≥ 10 μg / ml, they did not at the level of ≥ 5 μg / ml.

In the animal species examined, injections given at 2 sites appeared to influence the duration of predetermined serum drug levels more than the differences among the products in respect of the absorption and elimination rates from serum, the peak serum concentrations, and the dose. The shapes of the concentration‐to‐time curves in cows and ewes injected with the same dose of a given product were essentially the same, but they were different in goats. Serum chloramphenicol concentrations measured chemically after treatment with chloramphenicol base were 20% to 46% higher than those measured microbiologically.

For 60 minutes after the sodium succinate ester had been administered i.v. and i.m. to ewes, the chemically determined chloramphenicol levels were more than twice as high as the respective concentrations determined by microbiological assay, but thereafter, the magnitude of those differences was not greater than observed after treatment with chloramphenicol base.

Intramuscular bioavailability of the products containing chloramphenicol base injected at 2 sites was rather poor (51% to 80.5%ofthe dose) and even lower values were calculated after injection at a single site.

Results are briefly discussed of the effect of dosage form on the persistence of microbiologically effective serum drug levels. A dose of at least 50 mg / kg to be administered i.m. at two sites are essential prerequisits for chloramphenicol therapy in ruminants.