日本常规耕作和有机耕作(翻耕与免耕)农田的动物区系(螨和线蚓)比较

Nitrogen forms of humic substances from a subalpine meadow soil,a lateritic red soil and a weathered cola and the effect of acid hydrolysis on N structures of soil humic substances were studied by using ^15N cross-polarization magic angle spinning nuclear magnetic resonance(CPMAS NMR) spectroscopy,Of the detectable ^15N-signal intensity in the spectra of soil humic substances 71%-79% may be attributed to amide groups ,10%-18% to aromatic/aliphatic amines and 6%-11% to indole-and pyrrole-like N.Whereas in the spectrum of the fulvic acid from weathered coal 46%,at least,of the total ^15N-signal intensity might be assigned to pyrrole-like N,14% to aromatic/aliphatic amines,and the reamining intensities could not be assigned with certainty,Data on nonhydrolyzable reside of protein-sugar mixture and a ^15N-labelled soil fulvic acid confirm the formation of nonhydrolyzable heterocyclic N during acid hydrolysis.     

应用15N核磁共振技术对苯聚合物结合蛋白中氮形态的研究

Phenolic polymers synthesized by reactions by reactions of p-benzoquinone with 15N-labelled protein or (15NH4)2SO4 were studied by using 15N CP-MAS NMR technique in combination with chemical approaches.Results showed that more than 80% of nitrogen in quinone-protein polymers was in the form of amide with some present as aromatic and /or aliphatic amine and less than 10% of nitrogen occurred as heterocyclic N.The nitrogen distribution in the non-hydrolyzable residue of the quinone-protein polymers was basically similar to that of soil humic acid reported in literature with the exception that a higher proportion of N as heterocyclic N and aromatic amine and a lower proportion of N as amide and aliphatic amine were found in the former than in the latter,More than 70% of total nitrogen in quinone-(NH4)2OS4 polymer was acid resistant ,of which about 53% occurred as pyrrole,nitrile and imion type N.The possible roles of the reactions of phenols or quinones with proteins in the formation of humic acid.especially the non-hydrolyzable nitrogen in humicacid,are discussed.     

Nitrogen Forms in Synthetic Humic Acids Using Nitrogen-15 Nuclear Magnetic Resonance Technique

^15N-labelled phenolic polymers were synthesized by reactions of p-benzoquinone and 1,4-diphenol with ^15N-labelled glycine and were studied by using ^15N CP-MAS NMR technique in combination with chemical approaches.Results showed that the proportion of polymer nitrogen as N-phenyl amino acid N was not as great as expected,only accounting for 5%-15%;and most of N in polymers occurred in the forms of amide,pyrrole-and indole-like nitrogen,aliphatic amines and isonitrile.It seems that great differences existed between synthetic humic acids and soil humic acids in the type and distribution of nitrogen forms.     

Nitrogen Forms in Humic Substances

In this paper,the nitrogen forms in newly-formed humic substances,including humic acid (HA),fulvic acid (FA) and humic acid in humin (HAI),were studied by using the ^15N CP-MAS NMR technique in combination with chemical approaches.Results show that the majority of nitrogen in HA,FA and HAI was in the amide form with some presented as aliphatic and/ or aromatic amines and some as pyrrole type nitrogen,although the contents of nonhydrolyzable nitrogen in them differed greatly from each other (15-55%).     

固态13C和15N核磁共振法研究15N标记土壤的腐殖质组分

Five humic fractions were obtained from a uniformly ^15N-labelled soil by extraction with 0.1 mol L^-1 Na4P2O7,0.1mol L^-1 NaOH ,and HF/HCl-0.1 mol L^-1 NaOH,consecutively,and analyzed by ^13C and ^15N CPMAS NMR (cross polarization and magic angle spinning nuclear magnetic resonace).Compared with those of native soils humic fractions studied as a whole contained more alkyls ,methoxyls and O-alkyls,being 27%-36%,17%-21%and 36%-40%,respectively,but fewer aromatics and carboxyls(bein 14%-20% and 13%-90%,respectively),Among those humic fractions ,the humic acid(HA)and fulvic acid(FA) extracted by 0.1 mol L^-1 Na4P2O7 contained slightly more carboxyls than corresponding humic fractions extracted by 0.1 mol L^-1 NaOH ,and the HA extacted by 0.1 mol L^-1 NaOH after treatment with HF/HCl contained the least aromatics and carboxyls.The distribution of nitrogen functional groups of soil humic fractions studied was quite similar to each other and also quite similar to that of humic fraction from native soils.More than 75% of total N in each fraction was in amide from,with 9%-13% present as aromatic and /or aliphatic amines and the remainder as heerocyclic N.     

美国8种土壤的活性腐植酸和难溶性钙质腐植酸盐中碳官能团的特性分析

Solid state13C nuclear magnetic resonance(NMR)spectroscopy is a common tool to study the structure of soil humic fractions;however,knowledge regarding carbon structural relationships in humic fractions is limited.In this study,mobile humic acid(MHA)and recalcitrant calcium humate(CaHA)fractions were extracted from eight soils collected from six US states and representing a variety of soils and ecoregions,characterized by this spectroscopic technique and analyzed for statistical significance at P≤0.05.We found that the abundances of COO and N–C=O functional groups in the MHA fractions were negatively correlated to soil sand content,but were positively correlated to silt,total N and soil organic carbon contents.In contrast,the abundances of the COO and N–C=O functional groups were only positively correlated to the content of clay in the CaHA fractions,indicating that the two humic fractions were associated with diferent soil components.The two13C NMR peaks representing alkyls and OCH3/NCH were negatively correlated to the peaks representing aromatics,aromatic C–O and N–C=O/COO.Comparison of the sets of data from13C NMR spectroscopy and ultrahigh resolution mass spectrometry revealed that the aromatic components identified by the two methods were highly consistent.The comparison further revealed that protein in MHA was associated with,or bound to,the nonpolar alkyl groups,but a component competitively against(or complementary to)aromatic groups in the MHA composition.These observations provided insight on the internal correlations of the functional groups of soil humic fractions.     

土壤腐殖质氮结构的X-光电能谱研究

X－ray photoelectron spectroscopy(XPS) was applied to examine the N structures of soil humic substances and some of their analogues.It was found that for soil humic substances XPS method gave similar results as those obtained by ^15N CPMAS NMR (cross-polarization magic-angle spinning nuclear magnetic resonance) method.70%-86% of total N in soil humic substances was in the form of amide,and 6%-13% was presented as ammes,with the remaining part as heterocyclic N.There was no difference in the distribution of the forms of N between the humic substances from soils formed over hundreds or thousands of years and the newly formed ones.For fulvic acid from weathered coal and benzoquinone-(NH4)2SO4 polymer the XPS results deviated significantly from the ^15N CPMAS NMR data.     

Gaseous Loss of Nitrogen from Fertilizers Applied to a Paddy Soil in Southeastern China

Total nitrogen(N) loss and ammonia volatilization from urea applied to flooded rice grown on a paddy soil in Zhejiang Province were measured by ^15N balance and micro-meteorological methods,respectively.Floodwater properties and ammonia loss from the circular plot were compared with those from the microplots.And the effectiveness of urease inhibitor,NBPT [N-(n-butyl) thiophosphoric triamide],was also tested Results showed that the total losses from urea broadcast and incorporated at transplanting (basal dressing) were similar with those from urea broadcast 12 days after transplanting (top-dressing)(51.5% and 48%,respectively,of applied N),and ammonia losses were low,the corresponding figures were 10.8% and 7.0% of applied N,respectively.Thus,denitrification was a much more important pathway of nitrogen loss than ammonia volatilization under the particular conditions.Addition of NBPT retarded urea hydrolysis,reduced pHs and ammoniacal nitrogen concentrations of floodwater for either the application of urea as basal or as top-dressing,but these effects were not translated into the reduction of total nitrogen loss.Floodwater pHs and ammonia loss in the microplots were apparently lower than those in the circular plot from urea applied as basal dressing;however,such differences were not found when urea was top-dressed.The frequently raining days occurred after top-dressing may be responsible for the insignificant effect of plot size on floodwater pHs and ammonia volatilization.It seems that the effects of phot size on ploodwater properties and ammonia loss mainly depend on weather conditions,in addition to the height and leaf area index of the crop.     

中国洞庭湖区稻田土壤氮素淋溶损失的系统研究

A two-year lysimeter study was conducted to study the effects of different fertilizers and soils on nitrogen leaching loss in a double rice cropping system by considering three major types of paddy soils from the Dongting Lake area. The results showed that N concentration in the leachate did not differ significantly among the treatments of urea, controlled release N fertilizer and pig manure and that all these fertilizers produced higher total nitrogen (TN) concentrations in the leachate compared to the case where no fertilizer was applied. The TN leaching loss following urea treatment accounted for 2.28%, 0.66%, and 1.50% of the amount of N applied in the alluvial sandy loamy paddy soil (ASL), purple calcareous clayey paddy soil (PCC), and reddish-yellow loamy paddy soil (RYL), respectively. Higher TN loss was found to be correlated with the increased leachate volume in ASL compared with RYL, and the lowest TN loss was observed in the PCC, in which the lowest leachate volume and TN concentration were observed. Organic N and NH4+ -N were the major forms of N depleted through leachate, accounting for 56.8% and 39.7% of TN losses, respectively. Accordingly, soil-specific fertilization regimens are recommended; in particular, the maximum amount of fertilizer should be optimized for sandy soils with a high infiltration rate. To avoid a high N leaching loss from rice fields, organic N fertilizers such as urea or coated urea should primarily be used for surface topdressing or shallow-layer application and not for deep-layer application.     

15N标记的土壤估测某些豆科植物N2固定的温室实验

Pot experiments were carried out to estimate N2 fixation by vetch,milk vetch,sickle alfalfa and broadbean in pure stand using a ^15N-labelled soil.Winter wheat was used as the non-fixing control.The 15N-labelled soil used was prepared by growing corn-wheat-corn successively on a nearly organic-matter-free Xiashu loess supplemented with adequate amounts of (15NH4)2SO4,P,K and micronutrients,then incorporating these 15N-labelled plant materials into the soil after each havest,and allowing the plant materials to be decomposed aerobically for 410d after incorporation of the plant material of the thire crop.The 15N enrichment of wheat plant-N varied slightly with organs,with a maximum difference of 9.8%,Based on 15N enrichment of soil N inferred from the mean value of the 15N enrichment in different organs of wheat 79%-91% of total N in the tops and 67%-74% of total N in the roots of legumes studied were derived from atmosphere .Estimate by isotope dilution method was in good agreement with that by the conventional difference method provided values obtained by the latter were corrected for seed N,and also with that from the measurement of N accumulated in the tops of the legumes.     

利用137Cs估算土壤侵蚀速率的定量模型

A quantitative model was developed to relate the amount of ^137Cs loss from the soil profile to the rate of soil erosion,According th mass balance model,the depth distribution pattern of ^137Cs in the soil profile ,the radioactive decay of ^137Cs,sampling year and the difference of ^137Cs fallout amount among years were taken into consideration.By introducing typical depth distribution functions of ^137Cs into the model ,detailed equations for the model were got for different soil,The model shows that the rate of soil erosion is mainly controlled by the depth distrbution pattern of ^137Cs ,the year of sampling,and the percentage reduction in total ^137Cs,The relationship between the rate of soil loss and ^137Cs depletion i neither linear nor logarithmic,The depth distribution pattern of ^137Cs is a major factor for estimating the rate of soil loss,Soil erosion rate is directly related with the fraction of ^137Cs content near the soil surface. The influences of the radioactive decay of ^137Cs,sampling year and ^137Cs input fraction are not large compared with others.     

好氧条件下两种水稻土的氮素总转化速率比较

Although to date individual gross N transformations could be quantified by ~(15)N tracing method and models,studies are still limited in paddy soil.An incubation experiment was conducted using topsoil(0-20 cm) and subsoil(20-60 cm) of two paddy soils,alkaline and clay(AC) soil and neutral and silt loam(NSL) soil,to investigate gross N transformation rates.Soil samples were labeled with either ~(15)NH4_NO_3 or NH_4~(15)NO_3,and then incubated at 25 °C for 168 h at 60%water-holding capacity.The gross N mineralization(recalcitrant and labile organic N mineralization) rates in AC soil were 1.6 to 3.3 times higher than that in NSL soil,and the gross N nitrification(autotrophic and heterotrophic nitrification) rates in AC soil were 2.4 to 4.4 times higher than those in NSL soil.Although gross NO_3~- consumption(i.e.,NO_3~- immobilization and dissimilatory NO_3~- reduction to NH_4~+ rates increased with increasing gross nitrification rates,the measured net nitrification rate in AC soil was approximately 2.0 to 5.1 times higher than that in NSL soil.These showed that high NO_3~- production capacity of alkaline paddy soil should be a cause for concern because an accumulation of NO_3~- can increase the risk of NO_3~- loss through leaching and denitrification.     

可变电荷土壤和矿物Pb2+ and Cu2+吸附动力学: Ⅶ. Pb2+吸附后H+释放的动力学

The kinetics of H⁺ releasing after Pb²⁺ adsorption was studied by the potentiometric method combined with the acid-base titration curve technique. Results showed that pH of latosol, red soil and kaolinite suspensions dropped sharply, and then decreased gradually. Most of the H⁺ exchanged, more than 60%, was displaced at the first minute after Pb²⁺ was added into the suspension. More H⁺ was released at a higher concentration of Pb²⁺ added for a given sample and the amount of H⁺ released decreased in the order of red soil > latosol > kaolinite at a given concentration. The time-dependent data of H⁺ releasing of latosol, red soil and kaolinite at two concentrations could be fitted best with the second-order equation among the six equations, including second-order equation, two-constant equation, Elovich equation, parabolic diffusion equation, first-order equation and exponential equation. The H⁺/Pb²⁺ exchange stoichiometry increased with time, and a stable ratio of H⁺/Pb²⁺, being 1.73, 1.92 and 2.01 for kaolinite, latosol and red soil, respectively, was reached 25 minutes later.     

Effects of Irrigation Water Quality and Nitrogen Rate on the Recovery of 15N Fertilizer by Sorghum in Field Study

The effects of ¹⁵N-labeled ammonium nitrate on yield, uptake of nitrogen (N) by sorghum (Sorghum sudanense, Piper), and on N remaining in the soil were studied in a field experiment with different N rates (0, 50, and 100 kg N ha^?1) and with two irrigation water qualities, well water (WW) and treated wastewater (TWW). Treated wastewater irrigation increased dry matter and N yield compared to WW. At equal N rates, recovery of ¹⁵N-labeled fertilizer by plants increased with TWW irrigation compared to WW (36% versus 23%). Neither fertilizer rate nor water quality had an effect on the ¹⁵N-labeled fertilizer remaining in the 0- to 60-cm layer of soil. On average 41% in the TWW treatment (49–33%) and 38% in WW treatment was mostly present in the surface 20-cm layer. Losses of ¹⁵N-labeled fertilizer were unaffected by irrigation water quality (35%) and increased with N application rate in TWW (4% versus 31%).     

侵蚀引起的苏南坡地土壤退化

Soil erosion accelerates soil degradation. Some natural soils and cultivated soils on sloping land in southern Jiangsu Province, China were chosen to study soil degradation associated with erosion. Soil erosion intensity was investigated using the ¹³⁷Cs tracer method. Soil particle-size distribution, soil organic matter (OM), total nitrogen (TN) and total phosphorus (TP) were measured, and the effects of erosion on soil physical and chemical properties were analyzed statistically using SYSTAT8.0. Results indicated that erosion intensity of cultivated soils was greater than that of the natural soils, suggesting that cultivation increased soil loss. Erosion also led to an increase of coarser soil particle proportion, especially in natural soils. In addition, silt was the primary soil particle lost due to erosion. However, in cultivated fields, coarser soil particles over time were attributed not only to soil erosion but also to mechanical eluviation as a result of farming activities. Moreover, erosion caused a decrease in soil OM, TN and TP as well as thinning of the soil layer.     

红壤交换性钙、镁和钾的分布及施肥对其影响

A leaching experiment was Carried out with repacked soil columns in laboratory to study the leaching process of a red soil derived from sandstone as affected by various fertilization practices.The treatments were CK(as a control),CaCO3,CaSO4,MgCO3,Ca(H2PO4)2,Urea,KCl,Multiple(a mixture of the above mentioned fertilizers) and KNO3,The fertilizers were added to the bare surface of the soil columns,and then the columns were leached with 120 mL deionized water daily through perstaltic pumps over a period of 92 days,At the end of leaching process,soils were sampled from different depths of the soil profiles ,i.o.,of 92 days,At the end of leaching process,soils were sampled from different depths of the soil profiles,I.e.0-5cm,5-10cm,10-20cm,20-40cm,and 40-60cm,The results showed when applying Ca,Mg,and K to the bare surface of the soil columns,exchangeable Ca^2 ,Mg^2 ,and K^ in the upper layer of the soil profile increased correspondingly,with an extent depending mainly on the application rates of Ca,Mg,and K and showing a downward trend,CaCO3,CaSO4,MgCO3,and Ca(H2PO4)2 treatments had scarcely and effect on movement of exchangeable K^ ,while CaCO3,and CaSO4 treatments singnificantly promoted the downward movement of exchangealble Mg^2 although these two treatments had no obvious effect on leaching losses of Mg,The fact that under Urea treatment,exchangeable Ca^2 and Mg^2 ,were higher as compared to CK treatment showed urea could prevent leaching of exchangeable Ca^2 and Mg^2 ,the obvious downward movement of exchangeable Ca^2 and Mg^2 was noticed in KCl treatment ,In Multiple treatment,the downward movement of exchangeable Ca^2 and Mg^2 was evident,while that of K^ was less evident,Application of KNO3 strongly promoted the downward movement of exchangeable Ca^2 and Mg^2 in the soil profile.     

7Be: 中国贵州Hongfeng湖流域表土季节性侵蚀的地球化学示踪剂

7Be penetrative depth in undisturbed surface soil is within 4mm.^7Be activity shows exponential decrease with soil depth,which is expressed as a diffusion process.7Be penetrative depth in undisturbed surface soil is apparently deeper in the fall (0.22-0.37g cm^-1) than in the spring (0.11-0.28g cm^-2) at the same site;Whereas,^7Be apparent activity at the top of surface soil is higher in the spring (0.3-2.2Bq g^-1)than in the fall (0.2-0.5Bqg^-1) at the same site,The 7Be inventory(189-544Bq m^-2)changes with both locations and seasons.Although the ^7Be flux to the earth‘s surface increases with amount of precipitation,its maximum inventory in the soil profiles decreases to 30%-40% after the rainy period.Calculated by the diffusion equation,the erosion and accumulation rates of soil particles are agreeable with the observation in situ,Which shows that the rates in fall are 1.5 times those in spring.The eroded soil particles almost all have been removed on the tablelands rathel than transported into the drainage system.This indicates that the soil erosion process in the karst region is only partial transportation within a short distance.     

利用放射性碳对中国变性土的年代确定

Vertisols,which are mainly developed on fluvial and lacustrine deposits and basalt,are extensively distributed in China.66 samples of them for radiocarbon dating were collected across 5 porvinces and 1 autonomous region,ranging from warm-temperate to subtropical and tropical zones in China.The soil organic matter was dated via surface horizon,black soil horizon and dark-colour horizon of the vertisols,whereas carbonate through calcareous concretions and dispersed carbonate in soil profile using radiocarbon method.The present article elucidates the dates of genetic horizons,and of surface and buried vertisols as well.14C dating indicates that the surface vertisols were formed during the end of the late Pleistocene.ca.15600 years ageo.Correlation between depth of sampling and measured 14C age shows that age characteristics of the vertisols of China are close to those of West Germany,Italy,TUrnisia,Australia and Argentina,However,two buried vertisols developed on fluvial and lacustrine deposits were formed during different geological periods,The buried soils in warm-temperate zone were formed in the mid Holocene,while those in subtropics were buried at 12930 years B.P., and formed in the end of the late Pleistocene.