华北平原水浇玉米-小麦轮作农田氨挥发与反硝化损失

Ammonia (NH3) volatilization, denitriflcation loss, and nitrous oxide (N2O) emission were investigated from an irrigated wheat-maize rotation field on the North China Plain, and the magnitude of gaseous N loss from denitrification and NH3 volatilization was assessed. The micrometeorological gradient diffusion method in conjunction with a Bowen Ratio system was utilized to measure actual NH3 fluxes over a large area, while the acetylene inhibition technique (intact soil cores) was employed for measurement of denitrification losses and N2O emissions. Ammonia volatilization loss was 26.62% of the applied fertilizer nitrogen (N) under maize, while 0.90% and 15.55% were lost from the wheat field at sowing and topdressing, respectively. The differences in NH3 volatilization between different measurement events may be due to differences between the fertilization methods, and to differences in climatic conditions such as soil temperature. Denitrification losses in the fertilized plots were 0.67%-2.87% and 0.31%-0.49% of the applied fertilizer N under maize and wheat after subtracting those of the controls, respectively. Nitrous oxide emissions in the fertilized plots were approximately 0.08%-0.41% and 0.26%-0.34% of the applied fertilizer N over the maize and wheat seasons after subtracting those of the controls, correspondingly. The fertilizer N losses due to NH3 volatilization were markedly higher than those through denitriflcation and nitrous oxide emissions. These results indicated that NH3 volatilization was an important N transformation in the crop-soil system and was likely to be the major cause of low efficiencies with N fertilizer in the study area. Denitriflcation was not a very important pathway of N fertilizer loss, but did result in important evolution of the greenhouse gas N2O and the effect of N2O emitted from agricultural fields on environment should not be overlooked.     

加速土壤侵蚀对养分流失的影响

Soil erosion and nutrient losses on newly-deforested lands in the Ziwuling Region on the Loess Plateau of China were monitored to quantitatively evaluate the effects of accelerated soil erosion, caused by deforestation, on organic matter, nitrogen and phosphorus losses. Eight natural runoff plots were established on the loessial hill slopes representing different erosion patterns of dominant erosion processes including sheet, rill and shallow gully （similar to ephemeral gully）. Sediment samples were collected after each erosive rainfall event. Results showed that soil nutrients losses increased with an increase of erosion intensity. Linear relations between the losses of organic matter, total N, NH4-N, and available P and erosion intensity were found. Nutrient content per unit amount of eroded sediment decreased from the sheet to the shallow gully erosion zones, whereas total nutrient loss increased. Compared with topsoil, nutrients in eroded sediment were enriched, especially available P and NH4-N. The intensity of soil nutrient losses was also closely related to soil erosion intensity and pattern with the most severe soil erosion and nutrient loss occurring in the shallow gully channels on loessial hill slopes. These research findings will help to improve the understanding of the relation between accelerated erosion process after deforestation and soil quality degradation and to design better eco-environmental rehabilitation schemes for the Loess Plateau.     

运用双液相系统进行三氯苯的生物降解

Due to easy volatilization of volatile organic compounds from water,it is difficult to monitor their aerobic biodegradation in the traditional single water system.Whether a two-liquid-phase system(TLPS) could overcome this obstacle and enhance the degradation of volatile contaminants? In this study,a TLPS composed of silicone oil and water was employed to investigate the biodegradation of volatile compounds,trichlorobenzenes(TCBs),by the adapted microorganisms in an activated soil.The degradation and volatilization of TCBs in TLPS and in a single water system were compared.The results showed that due to volatilization losses of TCBs,the mass balance of TCBs in a single water system was very low.In contrast,using TLPS could effectively inhibit the volatilization losses of TCBs and achieved a very good mass balance during the biodegradation process.Meanwhile,the TLPS could increase microbial activity and microbial growth during the degradation process.With TLPS,the TCB degradation was in descending order of 1,2,4-TCB> 1,2,3-TCB>> 1,3,5-TCB,which was related to the exposed concentration of the contaminants in soil.This study showed that TLPS could be employed as an effective tool to evaluate the biodegradation of volatile hydrophobic organic compounds,which could not be achieved with the traditional single water system.     

不同耕作方式对紫色水稻土团聚体及有机碳分布的影响

The effect of different tillage systems on the size distribution of aggregates and organic carbon distribution and storage in different size aggregates in a Hydragric Anthrosol were studied in a long-term experiment in Chongqing, China. The experiment included three tillage treatments： conventional tillage with rotation of rice and winter fallow （CT-r） system, no-till and ridge culture with rotation of rice and rape （RT-rr） system, and conventional tillage with rotation of rice and rape （CT-rr） system. The results showed that the aggregates 0.02-025 mm in diameter accounted for the largest portion in each soil layer under all treatments. Compared with the CT-r system, in the 0-10 cm layer, the amount of aggregates 0.02 mm was larger under the RT-rr system, but smaller under the CT-rr system. In the 0-20 cm layer, the organic carbon content of all fractions of aggregates was the highest under the RT-rr system and lowest under the CT-rr system. The total organic carbon content showed a positive linear relationship with the amount of aggregates with diameter ranging from 0.25 to 2 mm. The storage of organic carbon in all fractions of aggregates under the RT-rr system was higher than that under the CT-r system in the 0-20 cm layer, but in the 0-60 cm soil layer, there was no distinct difference. Under the CT-rr system, the storage of organic carbon in all fractions of aggregates was lower than that under the CT-r system; most of the newly lost organic carbon was from the aggregates 0.002-0.02 and 0.02-0.25 mm in diameter.     

基施磷肥对石灰性土壤上番茄产量的影响

A lysimeter experiment with undisturbed soil profiles was carried out to study nitrogen cycling and losses in a paddy soll with applications of coated urea and urea under a rice-wheat rotation system in the Taihu Lake region from 2001 to 2003. Treatments for rice and wheat included urea at conventional, 300 （rice） and 250 （wheat） kg N ha^-1, and reduced levels, 150 （rice） and 125 （wheat） kg N ha^-1, coated urea at two levels, 100 （rice） and 75 （wheat） kg N ha^-1, and 150 （rice） and 125 （wheat） kg N ha^-1, and a control with no nitrogen arranged in a completely randomized design. The results under two rice-wheat rotations showed that N losses through both NH3 volatilization and runoff in the coated urea treatments were much lower than those in the urea treatments. In the urea treatments N runoff losses were significantly （P 〈 0.001） positively correlated （r = 0.851） with applied N. N concentration in surface water increased rapidly to maximum two days after urea application and then decreased quickly. However, if there was no heavy rain within five days of fertilizer application, the likelihood of N loss by runoff was not high. As the treatments showed little difference in N loss via percolation, nitrate N in the groundwater of the paddy fields was not directly related to N leaching. The total yield of the two rice-wheat rotations in the treatment of coated urea at 50% conventional level was higher than that in the treatment of urea at the conventional level. Thus, coated urea was more favorable to rice production and environmental protection than urea.     

Direct Estimation of Nitrogen Gases Emitted from Flooded Soils During Denitrification of Applied Nitrogen

Denitrification losses measured by direct method (measuring the evolution of (N2 N2O)-^15N) were compared with the apparent denitrification losses (calculated from the difference between the total N loss and ammonia loss), for fertilizers applied to flooded soils.The direct measured denitrification losses from potassium nitrate were 23.0%,40.0%,and 63.1-79.7% of applied N in rice field,and in incubations of 7 cm deep layer of soil and 2 cm deep layer of soil,respectively;while the corresponding apparent denitrification losses were 96.0%,98.4%,and 97.7-97.9%,respectively.In field experiments with urea,the direct measured denitrification losses ranged from 0.1-1.8%,which were much less than the apparent denitrification losses (41.3-45.7%).Such discrepancies were primarily due to the entrapment of the gaseous products of denitrification in the soil as revealed by the facts:(1) stirring the floodwater and the surface soil markedly increased the fluxes of (N2_N2O)-^15N from urea or potassium nitrate applied to the flooded rice field,and (2) reducing the pressure in the headspace of the incubation bottle with the 7 cm soil layer during gas sampling decreased the discrepance between the direct measured and apparent denitrifecation losses from 58.4% to 21.2%.The advantage of reducing the pressure in the headspace is that there is minimal disturbance of the soil.Further testing of this technique in rice field is needed to determine its effectiveness in releasing the entrapped gaseous products of denitrification so that denitrification losses can be quantified directly.     

硫酸盐对锌和镉在可变电荷土壤上吸附的影响

SO4^2- and Zn^2 or Cd^2 were added to three variable charge soils in different sequences.In one sequence sulfate was added first ,and in the other,Zn^2 or Cd^2 first.The addition of sulfate to the system invariably caused an increase in adsorption of the heavy metal added,with the effect more remarkable whn the soil reacted with the sulfate prior to the metal.the shift in pH50 for both Zn and Cd adsorption was aslo comparatively larger in the first sequence of reactions .It was suggested that the increase in negative charge density and the resultant negative potential of the soil were the primary cause of the pronounced effect of sulfate on adsorption of Zn or Cd,and the formaiton of the ternary surface complex-S-SO4-M might also play a role in the effect.     

石灰土壤原状土柱上硼和锌的迁移

Leaching of boron （B） and zinc （Zn） can be significant in some pedomorphic conditions, which can cause contamination of shallow groundwater and economic losses. Boron and Zn adsorption and transport was studied using 8.4 cm diameter × 28 cm long intact columns from two calcareous soil series with differing clay contents and vadose zone structures： Lyallpur soil series, clay loam （fine-silty, mixed, hyperthermic Ustalfic Haplargid）, and Sultanpur soil series, sandy loam （coarse-silty, mixed, hyperthermic Ustollic Camborthid）. The adsorption isotherms were developed by equilibrating soil with 0.01 tool L^-1 CaCl2 aqueous solution containing varying amounts of B and Zn and were fitted to the Langmuir equation. The B and Zn breakthrough curves were fitted to the two-domain convective-dispersive equation. At the end of the leaching experiment, 0.11 L 10 g L^-1 blue dye solution was also applied to each column to mark the flow paths. The Lyallpur soil columns had a slightly greater adsorption partition coefficient both for B and Zn than the Sultanpur soil columns. In the Lyallpur soil columns, B arrival was immediate but the peak concentration ratio （the concentration in solution at equilibrium/concentration applied） was lower than that in the Sultanpur soil columns. The breakthrough of B in the Sultanpur soil columns occurred after about 10 cm of cumulative drainage in both the columns; the rise in effluent concentration was fast and the peak concentration ratio was almost 1. Zinc leaching through the soil columns was very limited as only one column from the Lyallpur soil series showed Zn breakthrough in the effluent where the peak concentration ratio was only 0.05. This study demonstrates the effect of soil structure on B transport and has implications for the nutrient management in field soils.     

中国杉连作对土壤肥力的影响

The changes in soil fertility under continuous plantation of Chinese fir were studied by comparing soil samples from different forest stands:the first and second plantations of Chinese fir,evergreen broad-leaved forests,and clear-cut and burnt Chinese fir land located at Xihou Village,Nanping of Fujian Province.The soils were humic red soil originated from weathered coarse granite of the Presinian system.Soil pH,CEC,base saturation ,exchangeable Ca^2 ,exchangeable Mg^2 and A1-P declined after continuous plantation of Chinese fir.The same trends were also found in the soils under broad-leaved stands and slash burnt lands.The explantation was that not merely the biological nature of the Chinese fir itself but the natural leaching of nutrients,soil erosion and nutrient losses due to clear cutting and slash burning of the preceduing plantation caused the soil deterioration .Only some of main soil nutrients decreased after continuous plantation of Chinese fir,depending on specific silvicultural system,which was different from the conclusions in some other reports which showed that all main nutrients,such as OM,total N,available P and available K decreased,Some neccessary step to make up for the lost base,to apply P fertilizer and to avoid buring on clear cut lands could be taken to prevent soil degradation and yield decline in the system of continuous plantation of Chinese fir.     

集成定量方法用于同时监控密集型农业区域土壤侵蚀和非点源污染状况的研究

In China, some areas with intensive agricultural use are facing serious environmental problems caused by non-point source pollution（NPSP） as a consequence of soil erosion（SE）. Until now, simultaneous monitoring of NPSP and SE is difficult due to the intertwined effects of crop type, topography and management in these areas. In this study, we developed a new integrated method to simultaneously monitor SE and NPSP in an intensive agricultural area（about 6 000 km2） of Nanjing in eastern China, based on meteorological data,a geographic information system database and soil and water samples, and identified the main factors contributing to NPSP and SE by calculating the NPSP and SE loads in different sub-areas. The levels of soil total nitrogen（TN）, total phosphorus（TP）, available nitrogen（AN） and available phosphorus（AP） could be used to assess and predict the extent of NPSP and SE status in the study area.The most SE and NPSP loads occurred between April to August. The most seriously affected area in terms of SE and NPSP was the Jiangning District, implying that the effective management of SE and NPSP in this area should be considered as a priority. The sub-regions with higher vegetation coverage contributed to less SE and NPSP, confirming the conclusions of previous studies, namely that vegetation is an effective factor controlling SE and NPSP. Our quantitative method has both high precision and reliability for the simultaneous monitoring of SE and NPSP occurring in intensive agricultural areas.     

七种钾释放动力学方程的比较和动力学参数的应用

Batch equilibrium experiments were conducted to investigate cadmium （Cd） sorption by two permanent-charge soils, a yellow-cinnamon soil and a yellow-brown soil, and two variable-charge soils, a red soil and a latosol, with addition of selected organic acids （acetate, tartrate, and citrate）. Results showed that with an increase in acetate concentrations from 0 to 3.0 mmol L^-1, Cd sorption percentage by the yellow-cinnamon soil, the yellow-brown soil, and the latosol decreased. The sorption percentage of Cd by the yellow-clnnamon soil and generally the yellow-brown soil （permanent-charge soils） decreased with an increase in tartrate concentration, but increased at low tartrate concentrations for the red soil and the latosol. Curves of percentage of Cd sorption for citrate were similar to those for tartrate. For the variable-charge soils with tartrate and citrate, there were obvious peaks in Cd sorption percentage. These peaks, where organic acids had maximum influence, changed with soil type, and were at a higher organic acid concentration for the variable-charge soils than for the permanent charge soils. Addition of cadmium after tartrate adsorption resulted in higher sorption increase for the varlable-charge soils than permanent-charge soils. When tartrate and Cd solution were added together, sorption of Cd decreased with tartrate concentration for the yellow-brown soil, but increased at low tartrate concentrations and then decreased with tartrate concentration for the red soil and the latosol.     

可变电荷或永久电荷土壤上的电荷特征与土壤对Cu2+的吸附－解吸之间的交互作用

Charge characteristics and Cu^2 adsorption-desorption of soils with variable charge(latosol)and permanent charge(brown soil)and the relationship between them were studied by means of back-titration and adsorption equilibrium respectively.The amount of variable negative charge was much less in variable-charge soil than in permanent-charge soil and increased with the pH in the system,but the opposite trend occurred in the points of zero charge(PZCs).The amount of Cu^2 ions sorbed by permanent-charge soil was more than that by variable-charge soil and increased with the increase of Cu^2 concentration within a certain range in the equilibrium solution.The amount of Cu^2 ions desorbed with KCl from permanent-charge soil was more than that from variable-charge soil,but the amount of Cu^2 ions desorbed with de-ionized water from permanent-charge soil was extremely low whereas there was still a certain amount of desorption from variable-charge soil.The increase of PZC of soils with variable or permanent change varied with the increment of Cu^2 ions added.When the same amount of Cu^2 ions was added,the increments of PZC and variable negative surface chargc of permanent-charge soil were different from those of variable-charge soil.     

有机酸对土壤中镉的解吸及影响因素

研究了酒石酸和柠檬酸对两种不同处理土壤 (镉质土和污染土 )中Cd的解吸行为 ,探讨了介质pH值、支持电解质等对其解吸镉质土和污染土中Cd的影响。结果表明 ,随有机酸浓度升高 ,柠檬酸和酒石酸对镉质土和污染土中Cd的解吸率呈先降低后升高变化 ,出现一波谷 ,波谷位置与有机酸和土壤类型有关。当解吸液起始pH值由 2升至 8时 ,柠檬酸对镉质土和污染土中Cd的解吸率呈降低—升高—降低的变化 ,先后出现一波谷和一波峰 ,且柠檬酸浓度高时变化趋势尤为明显 ;而酒石酸对镉质土和污染土中Cd的解吸率则一直降低。解吸液中支持电解质浓度提高 ,酒石酸对镉质土和污染土中Cd的解吸率增大 ,且以KCl为支持电解质时的解吸率要高于KNO3。     

共存阳离子（Ca、Zn、K）对土壤镉有效性的影响

采用盆栽与吸附试验,研究了镉污染赤红壤上,施用相同摩尔浓度的钙、钾与锌对小油菜生物量、镉吸收量及土壤镉吸附的影响。结果表明,低和高镉污染赤红壤上,施用锌明显增加小油菜地上部生物量,较对照分别增产21.1%和7.82%。不同阳离子（钠、钙、钾和锌离子）共存改变土壤吸附镉能力的程度不同,与钠体系相比,钙、钾和锌体系中土壤镉吸附量分别降低65.6%、72.0%和96.9%,共存离子降低土壤镉吸附量的次序为锌离子〉钾离子和钙离子,锌离子的影响最为明显。高镉污染赤红壤上,钙和钾使小油菜吸镉量分别增加5.5%和14.4%,低于低镉污染赤红壤上钙和钾使小油菜吸镉的增加量（分别为16.6%和19.6%）;锌明显降低小油菜吸镉量,高和低镉污染赤红壤上,较对照分别减少45.8%和35.0%。3种阳离子与镉共存时,对土壤镉生物有效性的影响差异取决于竞争吸附与竞争吸收的大小,其机制有待进一步探讨。     

Solubility,sorption and desorption of native and added cadmium in relation to properties of soils in New Zealand

Solution cadmium (Cd) concentrations and sorption and desorption of native and added Cd were studied in a range of New Zealand soils. The concentration of Cd in solution and the concentrations and patterns of native soil Cd desorbed and added Cd sorbed and desorbed varied greatly between the 29 soils studied. Correlation analysis revealed that pH was the most dominant soil variable affecting solution Cd concentration and sorption and desorption of native and added Cd in these soils. However, organic matter, cation exchange capacity (CEC) and total soil Cd were also found to be important. Multiple regression analysis showed that the log concentration of Cd in solution was strongly related to soil pH, organic matter and total Cd, which in combination explained 76% of the variation between soils. When data from the present study were combined into a single multiple regression with soil data from a previously published study, the equation generated could explain 81% of the variation in log Cd solution concentration. This reinforces the importance of pH, organic matter and total Cd in controlling solution Cd concentrations. Simple linear regression analysis could at best explain 53% of the total variation in Cd sorption or desorption for the soils studied. Multiple regression analysis showed that native Cd desorption was related to pH, organic matter and total Cd, which in combination explained 85% of the variation between soils. For sorption of Cd (from 2 μg Cd g^–1 soil added), pH and organic matter in combination explained 75% of the variation between soils. However, for added Cd desorption (%), pH and CEC explained 77%. It is clear that the combined effects of a range of soil properties control the concentration of Cd in solution, and of sorption and desorption of Cd in soils. The fraction of potentially desorbable added Cd in soils could also be predicted from a soil’s K_d value. This could have value for assessing both the mobility of Cd in soil and its likely availability to plants.     

海泡石对典型水稻土镉吸附能力的影响

通过吸附解吸实验研究了添加海泡石后典型水稻土对Cd的吸附解吸特性及其对吸附溶液pH值变化的响应。结果表明,Freundlich方程可以较好地拟合红黄泥、黄泥田和红沙泥3种典型水稻土对Cd的等温吸附过程（R2〉0.962）。在溶液初始Cd浓度相同的情况下,添加海泡石可使3种水稻土对Cd的吸附量增加20%以上,增强土壤对Cd的吸附强度,有效降低吸附Cd的解吸率,其效果随海泡石添加量的增大而增强。3种水稻土吸附Cd的解吸率均高于70%,而且都随吸附量的增加而上升。溶液的pH值是影响土壤吸附Cd的一个重要因素,在低pH值的条件下（pH〈4）,随着溶液pH值的降低,土壤对Cd的吸附量迅速降低,当溶液pH值高于5时,pH值的变化对吸附量的影响较小。在溶液初始pH值2-8范围内,添加海泡石均能有效提高3种水稻土对Cd的吸附能力。     

华中南部某些土壤针铁矿的形态

The morphologies of goethites in latosol, red soils, yellow-brown soil and the paddy soils developed from red soils were studied in comparison with the morphology of synthetic goethite by means of the X-ray diffraction, transmission electron microscopy and energy dispersive X-ray analysis. The synthetic goethite displayed acicular particles elongated in the c-direction. The goethites in the latosol, red soils and yellow-brown soil were platy particles stretched in two directions or isodimensional particles, and those in the paddy soils from red soils were acicular, short columnar, platy or isodimensional particles. Various morphologies of the goethites probably suggested their different dominant crystal faces, surface charge distribution and surface adsorption characteristics.     

有机质对红壤和黑土中外源铅镉稳定化过程的影响

采用室内培养方法研究了中国典型红壤和黑土中外源铅（Pb）、镉（Cd）在单一和复合污染下的稳定化过程,探讨了土壤有机质含量对Pb、Cd稳定化过程的影响。结果表明,加入500mg·kg-1Pb、1.0mg·kg-1Cd或1.0mg·kg-1Cd＋500mg·kg-1Pb条件下,各种土壤有效态Pb、Cd含量在培养前期迅速下降,随后变化减缓,培养30d后基本达到平衡。利用二级动力学方程对Pb、Cd稳定化过程进行拟合,在红壤和黑土上,有机质含量高的土样有效态Cd的平衡浓度比有机质含量低的土样中降低12.7%～37.3%;有效态Pb的平衡浓度比有机质含量低的土样中降低78.3%～96.2%,相关分析表明,土壤有机质含量的增加显著抑制了外源Pb、Cd的有效性（P〈0.05）。在铅镉复合污染中,Pb的存在提高了土壤中Cd的有效性,而Cd对Pb的影响较小。与黑土相比,红壤上外源Pb、Cd稳定化速率较小,达到平衡所需的时间较长,且有效态Pb、Cd的平衡浓度较高。因此,在农业生产实践中,通过提高红壤和黑土上有机质的含量能够显著降低外源重金属Pb、Cd的有效性,减少环境污染风险。     

几种有机酸对恒电荷和可变电荷土壤吸附Cu2+的影响

以恒电荷土壤(黄褐土和黄棕壤)和可变电荷土壤(红壤和砖红壤)为供试材料,研究了乙酸、草酸、酒石酸和柠檬酸对土壤吸附重金属铜离子(Cu2 )的影响。结果表明,在相同酒石酸浓度下,土壤对酒石酸的吸附量依次为黄棕壤(2 1 8mmolkg-1) >红壤(15 4mmolkg-1) >砖红壤(9 5mmolkg-1) ,土壤吸附有机酸后负电荷量增加,相同条件下增幅为砖红壤>红壤>黄棕壤;无有机酸配体时,供试土壤对Cu2 的吸附量为黄褐土>黄棕壤>砖红壤>红壤;加入有机酸时,随有机酸浓度增高,土壤对Cu2 的吸附一般表现为“峰”形曲线,峰所对应的有机酸浓度因有机酸类型而异,且随土壤可变电荷性质增强而增高;土壤吸附有机酸后对Cu2 的次级吸附不同于有机酸与铜共存时的竞争吸附,且因土壤性质表现迥异。这些结果意味着在存在有机酸配体的根际环境中,恒电荷土壤与可变电荷土壤对Cu2 的吸附明显不同,并将影响重金属离子在根际的转化与有效性     

蒸腾潜能的模型研究及估算中国土壤湿度状况

The morphologies of goethites in latosol,red soils,yellow-brown soil and the paddy soils developed from red soils were studied in comparison with the morphology of synthetic goethite by means of the X-ray diffration,transmission electron microscopy and energy dispersive X-ray analysis.The synthetic goethite displayed acicular particles elongated in the c-direction.The goethites in the latosol,red soils and yellowbrown soil were platy particles stretched in two directions or isodimensional particles,and those in the paddy soils from red soils were acicular,short columnar,palty or isodimensional particles,Various morphologies of the goethites probably suggested their different dominant crystal faces,surface charge distribution and surface adsorption characteristics.