一种模拟土壤养分提取及及植物吸收的装置研究

In situ evaluating the availability of soil nutrients has been a challenge. In this study, a new type of Device for Simulating Soil Nutrient Extraction and Plant Uptake (DSSNEPU) and its operating procedures were introduced. The device consists of a sampling tube, a fluid supply system, a low pressure system, a tube sheath and an elution cylinder. The sampling tube was firstly soaked in the solution of 0.5 mol L 1 NaHCO 3 and then buried into soils. The fluid supply system was connected to the sampling tube and the deionized water was supplied. During the period, low pressure system started a vacuum for 3 min every 10 min interval. After extraction, the sampling tube was removed and the nutrients on the sampling tube were eluted with 0.5 mol L 1 HCl. The elution solution was used for nutrient measurement. The amounts of P and K extracted by DSSNEPU reached the maximal values after 4 h. No significant increases of P and K were observed for longer extraction duration. The optimal temperature for extracting P and K was 30 C in this experiment. Extracted P and K were increased by 83.3% and 84.6% with the employment of low pressure system in comparison to those without employing low pressure system. Correlation analysis indicated that P and K extracted by DSSNEPU were highly correlated with those by conventional chemical extraction and by plant uptake. The above results suggest that this device is applicable to assess the availability of nutrients in soils.     

土壤中磷、钾、钙、镁的同时提取以及对巴西南部作物的钾肥推荐

Simultaneous multi-element extraction has been increasing worldwide to improve soil laboratory testing quality and effciency. This study sought to investigate the applicability of the Mehlich-1, Mehlich-3, and resin methods for simultaneous extraction of soil available P, K, Ca, and Mg as well as the effect of using conversion equations on nutrient recommendations for crops. Topsoil (0-20 cm) samples were taken from the most representative soil types used for crop production in southern Brazil with a wide range of chemical, physical, and mineralogical properties. Soil P, K, Ca, and Mg were simultaneously extracted using 1.0 mol L-1 KCl, Mehlich-1 and Mehlich-3 solutions, and membrane resin. The amounts of P extracted with the Mehlich-1 method were, on average, 50% lower than those extracted with the resin and Mehlich-3 methods. However, the resin method extracted the lowest amounts of K, Ca, and Mg. The use of conversion equations was suitable and it did not a?ect negatively the K recommendations for crops grown on soils of southern Brazil.     

澳大利亚东部地区一些酸性硫酸盐土壤磷的特征

Forty-five acid sulfate topsoil samples (depth < 0.5 m) from 15 soil cores were collected from 11 locations along the New South Wales coast, Australia. There was an overall trend for the concentration of the HC1-extractable P to increase along with increasing amounts of organic C and the HCl-extractable trivalent metals in the topsoils of some less-disturbed acid sulfate soils (pH < 4.5). This suggests that inorganic P in these soils probably accumulated via biological cycling and was retained by complexation with trivalent metals or their oxides and hydroxides. While there was no clear correlation between pH and the water-extractable P, the concentration of the water-extractable P tended to increase with increasing amounts of the HCl-extractable P. This disagrees with some established models which suggest that the concentration of solution P in acid soils is independent of total P and decreases with increasing acidity. The high concentration of sulfate present in acid sulfate soils appeared to affect the chemical behavior of Pin these soil systems. Comparison was made between a less disturbed wetland acid sulfate soil and a more intensively disturbed sugarcane acid sulfate soil. The results show that reclamation of wetland acid sulfate soils for sugarcane production caused a significant decrease in the HCl-extractable P in the topsoil layer as a result of the reduced bio-cycling of phosphorus following sugarcane farming. Simulation experiment shows that addition of hydrated lime had no effects on the immobilization of retained P in an acid sulfate soil sample within a pH range 3.54.6. When the pH was raised to above 4.6, soluble P in the soil extracts had a tendency to increase with increasing pH until the 15th extraction (pH 5.13). This, in combination with the poor pH-soluble P relationship observed from the less-disturbed acid sulfate soils, suggests that soluble P was not clearly pH-dependent in acid sulfate soils with pH < 4.5.     

中性盐和pH对红壤、砖红壤胶体交换性酸的影响

In the present work, the exchangeable acidity of a red soil colloid and a latosol colloid at different pH during reacting with four neutral salts was measured. The results show that the exchangeable acidity increased with increasing amounts of the neutral salts added, and the relation between them was almost linear. When the amount of the neutral salt added was lower than a certain value, the slope of the line was high, and the slope turned low when the amount exceeded that value, so there was a turning point in each line. The addition amounts of the neutral salts for the turning points were affected by the cation species of the neutral salts, but pH had less effect on them. After the turning points occurred, the exchangeable acidity of the red soil colloid still gradually increased with the addition amounts of the neutral salts, but that of the latosol colloid did not increase any more. The exchangeable acidity in NaClO₄, KClO₄ and NaCl solutions increased at first, and then decreased with increasing pH, that is to say, peak values appeared. The peak positions of the exchangeable acidity in relation to pH changed with neutral salt solutions and were affected by the surface characteristics of the soil colloids, but not affected by the amounts of the neutral salts added. The exchangeable acidity in the Ba(NO₃)₂ solution increased continuously with increasing pH. The exchangeable acidity of the red soil colloid was obviously larger than that of the latosol colloid.     

Studies on Material Cycling in Evergreen Broad-Leaved Forest Ecosystem in Hangzhou: Ⅰ. Precipitation Distribution

Through the long-term plot studies plot studies on the precipitation distribution in the evergreen broad-leaved forest ecosystem in Hangzhou for two years,it was indicated that the pattern of precipitation distribution included larger amounts of penetration water and stemflow and a lower amount of interception water.The results revealed that the main factors to infulence the percentages of penetration and stemflow were the air temperature and the leaf area of the forest.The quantity of seepage through the litter layer was much larger than that through the soil layers which decreased sharply with soil depth.The output of water from the ecosystem by surface runoff and deep infiltration through the soil was much lower,only being 5.20 percent of the rainfall,while the water evapotranspiration loss was as large as more than 90 percent of it.The losses by the soil evaporation and plant evapotranspiration were the largest part of output in this forest ecosystem.     

某极度酸化的酸性硫酸盐土壤中可溶性和交换性酸的特征

An extremely acidified acid sulfate soil(ASS) was investigated to characterise its soluble and exchangeable acidity,The results showed that soluble acidity of a sample dtermined by titration with a KOH soulution was much significantly greater than that indicated by pH measured using a pH meter,paricularly for the extremely acidic soil samples,This is because the total soluble acidity of the extremely acidic soil samples was mainly composed of various soluble Al and Fe species,possibly in forms of Al sulfate complexes(e.g.,AlSO4^ ) and feerous Fe(Fe^2 )_,It is therefore suggested not to use pH alone as an indicator of soluble acidity in ASS,particularly for extremely acidic ASS,It is also likely that AlSO4^ actively participated in cation exchange reactions.It appears that the possible involvement of this Al sulfate cation in the cation adsorption has significant effect on increasing the amount of acidity being adsorbed by the soils.     

土-水体系中Hg的垂直迁移

Hg vertical transference in soil-water system w as studied by analyzing Hg vertical distribution in soil column after adding Hg and one of the two leacheates, deionized water or acid rain, into soil column. The results indicated that Hg was hardly transferable in purple soil. About 86% ~ 88% of the total soil Hg was distributed in the top layer (0~2 cm) and no Hg was detected in the leakage when the purple soil column was leached by deionized water and simulated acid rain. But Hg was more movable in yellow soil with only about 20%~22% of the total soil Hg distributed in the top layer (0~2 cm), and about 17%~25% washed out from the soil column by deionized water and simulated acid rain. Increment in soil bulk density could reduce Hg leaching, thus the more the Hg kept in soil, the less the Hg leached into underground water. Deionized water and acid rain almost played the same role in leaching Hg. Bentonite was most efficient in preventing Hg from vertical transferring in the soil column.     

Release of Soil Nonexchangeable K by Organic Acids

The amounts of soil nonexchangeable K extracted with 0.01mL/L oxalic acid and citric acid solutions and that with boiling 1mL/L HNO3 for ten minutes were remarkably significantly correlated with each other,and the amount extracted with the oxalic acid solution was higher than that with the citric acid solution.The soil nonexchangeable K release was comprised of two first-order kinetic processes.The faster one was ascribed to the interlayer K in outer sphere,while the slower one to that in inner sphere.The rate constants of the soil nonexchageable K were significantly correlated with the amounts of nonexchangeable K ex tracted with boiling 1mL/L HNO3 for ten minutes.Study on the fitness of different kinetic equations indicated that the first-order,parabolic diffusion and zero-order equations could all describe the release of soil nonexchangeable K well,but Elovich equation was not suitable to describe it.     

稻田土壤甲烷排放模型: Ⅱ. 模型的验证和应用

Fifteen upland soils collected from the major arable areas in NOrth China were used to assess the availability of soil sulfur(S) to plants in a pot experiment.Soils were extracted with various reagents and the extractable S was determined using turbidimetric method or inductively coupled plasma atomic emission spectrometry (ICP-AES),respectively.In addition,mineralizable organic S,organic S,N/S ratio,sulfur availability index(SAI) and available sulfur correction value(ASC) in soils were also determined.The S amout extracted by 1.5g L^-1 CaCl2 was nearly equivalent to that by 0.25mol L^-1 KCl(40℃),and both of them were slightly smaller than that by 0.01 molL^-1 Ca(H2PO4)2 solution,as measured by turbidimetric method or ICP-AES.The extractable S measured by turbidimetric method was consistently smaller than that by ICP-AES.All methods tested except that for organic S and N/S ratio produced satisfactoy results in the regression analyses of the relationships between the amounts of S extracted and plant dry matter weight and S uptake in the pot experiment,In general,0.01 mol L^-1 Ca(H2PO4)2-extracted S determined by ICP-AES or turbidimetric method and 0.25mol L^-1 KCl(40℃)-extracted S determined by ICP-AES appeared to be the best indicators for evaluation of soil available S.     

中国亚热带地区酸性土壤上部分酸化的磷矿石的农学潜力

A glasshouse experiment was conducted to evaluate the agronomic potential of four partially acidulated rock phosphates(PARP) in three representative solis sampled from subtripical China.The PARPs were manufactured by attacking a moderately reactive phosphate rock either with sulfuric acid alone or with combination of sulfuric and phosphoric acids at 30 or 60 percent of acidulation.Shoot dry weight and P accumulation of six successive cuttings of ryegrass were used to compare the agronomic potential of these fertilizers with that of the raw rock phosphate(RP) and monocalcium phosphate (MCP).Results indicated that the effectiveness of various phosphates was determined both by the solubility of the phosphates and by the acidity and P-fixing capacity of the soils.The higher the watersoluble P contained,the better the effectiveness of the fertilizer was.Although plant P accumulation of PARP treatments was constantly lower than that of MCP treatment,some PARPs could still get a dry matter production similar to that of MCP treatment.PARP SP60,which was acidulated with a mixture of sulfuric acid and phosphoric acid at 60 percent of acidulation and contained the highest soluble,P,was as effective as MCP in terms of dry matter production on all the soils.S60 and C1 which were both acidulated with sulfuric acid with the former at 60 percent of acidulation and the latter at 30 percent but with a further addition of monoammonium phosphate,were more than 80 percent as efective as MCP,Raw RP also showed a reasonable effectiveness which increased with soil acidity.It was suggested from the study that some of these APRPs could be expected to have a comparable field performance as soluble P fertilizers in the acid soil regions.     

草酸和酒石酸促进花岗岩中钾释放的实验研究

利用浸提实验研究了草酸和酒石酸作用下花岗岩中钾的释放量与低分子量有机酸种类、浓度和时间的关系,同时讨论了释放出来的钾的可能来源。研究结果表明:草酸浸提钾的能力强于酒石酸,在相同的条件下草酸浸提的钾量是酒石酸的2~27倍;在0.005~0.500 mol L-1浓度范围内,浸提的钾量随着有机酸浓度的升高而增大;浸提的钾量随着浸提时间的延长而增大,最后趋于稳定;在实验过程中,花岗岩的矿物组成未发生明显的变化,说明进入到溶液中的钾并非来自晶格内部,很有可能是来自于正长石、白云母表面及其边缘断键。     

酸性土壤有效汞提取方法研究

为了更好地评价酸性土壤中汞的生物有效性和生态风险,以酸性土壤为供试土壤,通过比较国内外几种常用的土壤有效汞的浸提剂的提取效果,筛选适合于酸性土壤的有效汞浸提剂并优化相应的提取条件,从而建立酸性土壤有效汞的提取方法。结果表明,在0.1 mol·L-1HCl、1 mol·L-1NH4OAc、0.005 mol·L-1DTPA、0.03%TGA-1/15 mol·L-1Na2HPO4这4种常用浸提剂中,0.03%TGA-1/15 mol·L-1Na2HPO4是最佳的浸提剂,因为它具有最高的提取率,且其所提取的有效汞与相应稻米中Hg含量的相关性最好。0.03%TGA-1/15 mol·L-1Na2HPO4的最佳浸提条件为土液比1∶10、振荡时间120 min、振荡速度250 r.min-1,浸提出的有效汞量与油菜的相关性达到极显著相关,能较好地指示田间条件下土壤汞对作物的可给性。     

乙二胺四乙酸和柠檬酸活化石灰性土壤磷素的潜力评估

  【目的】  长期施磷形成的高磷残留土壤,面临土壤酸化、钙镁离子淋失等问题。本研究采用肥料中常见的螯合剂乙二胺四乙酸 (EDTA) 和柠檬酸,研究其对不同磷含量的石灰性土壤中磷素的活化作用,以期为磷肥减施和土壤残留磷高效利用提供有效途径。  【方法】  供试低磷、高磷和白云石改良土壤取自北京市房山区的石灰性土壤,3种供试土壤的全磷含量依次为0.95、1.90和1.91 g/kg,有效磷含量依次为7.39、160和152 mg/kg。采用室内往复振荡浸提方法,两种浸提剂为EDTA和柠檬酸,低磷土壤浸提剂浓度为0.05 g/L,浸提时间为12 h,高磷土壤和改良土壤浸提剂浓度均为0.5 g/L,浸提时间分别为12 h和1 h。每个土壤样品采用相同方法连续浸提10次,同时以去离子水浸提作为对照。测定了浸提液中磷、钙、镁、铁、铝含量,计算各元素的单次浸提量和累积浸提量。全部浸提后,用蒋顾磷分组法测定了土壤中不同组分磷的含量。  【结果】  EDTA和柠檬酸在低磷土壤中单次磷素浸提量均较低,且累积浸提量之间差异不显著,连续浸提10次后磷素的累积浸提量不及土壤全磷的3%;而在高磷土壤和施入白云石的改良土壤中,柠檬酸和EDTA的单次磷素浸提量为低磷土壤的7～64倍,磷素累积浸提量超过土壤总磷的20%,且柠檬酸处理高于EDTA处理。在低磷土壤中,磷素的累积浸提量仅与铁和铝离子的累积浸提量显著相关,在高磷土壤中,磷素的累积浸提量与钙、镁、铁和铝离子的累积浸提量均显著正相关,且相关系数均在0.78以上,而在白云石改良土壤中,磷素的累积浸提量与铝离子的累积浸提量之间无显著相关关系。进一步分析浸提前后土壤磷素组分变化可知,在低磷土壤中,去离子水、EDTA和柠檬酸经10次浸提后土壤Ca₂-P显著增加;在高磷土壤中,EDTA和柠檬酸处理浸提的土壤Ca₂-P、Ca₈-P较去离子水处理显著降低了16.1%、14.9%和37.1%、5.4%。此外,柠檬酸处理还降低了31.4%的土壤Al-P,EDTA和柠檬酸在改良土壤上对于各组分磷的浸提量与在高磷土壤上相似。  【结论】  在连续浸提的条件下,EDTA 和柠檬酸在低磷土壤上无明显活化磷素的效果,而在高磷土壤上和施入白云石的改良土壤上则可持续浸提出大于总磷量20%的磷素。高磷土壤和改良后土壤中被浸提磷素主要来自Ca₂-P和Ca₈-P,少部分来自Al-P和Fe-P。     

Comparison of Prewashing Procedures for the Assessment of Phosphate Rock Dissolution in Soils

When evaluating phosphate rock (PR) dissolution, previous to the extraction with sodium hydroxide (NaOH), dry soil samples with PR were extracted with three solutions to remove exchangeable and solution calcium (Ca) [sodium chloride (NaCl) 1 M, buffered NaCl with ethylenediaminetetraacetic acid (EDTA) (NaCl–EDTA), and NaCl buffered at pH 7 with triethanolamine (TEA) (NaCl–TEA)] for comparison with the extraction of soil samples without any prewash. In acidic soils, up to 51% of applied P was recovered during the NaCl extraction because of the high exchangeable acidity released during the extraction. In soils with exchangeable Ca>2 cmol₍₊₎kg^?1, high EDTA quantities also promoted PR dissolution. The NaCl–TEA solution efficiently removed Ca, avoiding PR dissolution and P retention by calcium hydroxide [Ca(OH)₂] during the NaOH extraction. Thus, when evaluating PR dissolution we recommend the use of NaCl–TEA to remove Ca. We also recommend the same procedure when applying the Chang and Jackson fractionation to calcareous soils and soils submitted to PR application.     

动力学模型在土壤钾素释放特征描述中的运用及其与化学方法提取的钾素之间的相关性研究

Potassium (K) release characteristics in soil play a significant role in supplying available K. Information on K-release characteristics in soils of central Iran is limited. The objectives of this study were to determine K release characteristics and correlations of K release rate constants with K extracted by different chemical methods in surface soils of ten calcareous soils of central Iran. The kinetics of K release in the soils was determined by successive extraction with 0.01 mol L^-1 CaCl₂ in a period of 2--2 017 h at 25±1 ^oC. Soil K was extracted by distilled water, 0.5 mol L-1 MgNO₃, 0.002 mol L^-1 SrCl₂, 0.1 mol L^-1 BaCl₂, 0.01 mol L^-1 CaCl₂, 1 mol L^-1 NaCl, 1 mol L^-1 boiling HNO₃, 1 mol L^-1 NH₄OAC, Mehlich 1, 0.002 mol L^-1 SrCl₂ 0.05 mol L^-1 citric acid, and ammonium bicarbonate-diethylenetriamine pentaacetic acid (AB-DTPA). A plot of cumulative amounts of K released showed a discontinuity in slope at 168 h. Thus, two equations were applied to two segments of the total reaction time (2--168 and 168--2017 h). Cumulative amounts of K released ranged from 55 to 299 mg kg^-1 in 2--168 h and from 44 to 119 mg kg^-1 in 168--2 017 h. Release kinetics of K in the two time segments conformed fairly well to parabolic diffusion, simplified Elovich, and power function models. There was a wide variation in the K release rate constants. Increasingly higher average concentrations of soil K were extracted by distilled water, Mehlich 1, SrCl₂, CaCl₂, SrCl₂ + citric acid, AB-DTPA, MgNO₃, NaCl, NH₄OAc, BaCl₂ and HNO₃. Potassium release rate constants were significantly correlated with K extracted. The results of this study showed that information obtained from mathematical modeling in two reaction time segments can help to estimate the K-supplying power of soils.     

柠檬酸对高岭石的溶解作用

采用间歇法(batch method)研究柠檬酸对高岭石溶解的影响。结果表明:低浓度(0.02mmolL-1)柠檬酸可促进高岭石中Ca2+、Mg2+、Na+少量的释放。当柠檬酸浓度分别为1.0mmolL-1和8mmolL-1时,Ca2+,Mg2+,K+,Na+,Si,Al3+阳离子的释放量也相应地增加。释放的Ca2+、Mg2+主要来自高岭石表面的吸附,而Na+、K+则来自高岭石的溶解。     

外来种互花米草对江苏省潮间带生物地球化学过程的影响研究

Spartina alterniflora Loisel, a species vegetating in intertidal flats along the eastern coast of the United States, was introduced in China almost 30 years ago and has become an urgent topic due to its invasiveness in the coastal zone of China. The impacts of this alien species S. alterniflora on intertidal ecosystem processes in the Jiangsu coastland were investigated by comparing the sediment nutrient availability and trace element concentration characteristics in a mud flat and those of a four-year old Spartina salt marsh that had earlier been a mudflat. At each study site, fifteen plots were sampled in different seasons to determine the sediment characteristics along the tidal flats. The results suggested that Spartina salt marsh sediments had significantly higher total N, available P, and water content, but lower pH and bulk density than mudflat sediments. Sediment salinity, water content, total N, organic C, and available P decreased along a seaward gradient in the Spartina salt marsh and increased with vegetation biomass. Furthermore, the concentrations of trace elements and some metal elements in the sediment were higher under Spartina although these increases were not significant. Also, in the Spartina marsh, some heavy metals were concentrated in the surface layer of the sediment. The Spartina salt marsh in this study was only four years old; therefore, it is suggested that further study of this allen species on a longer time frame in the Jiangsu coastland should be carried out.     

Analysis of sulfur compounds in acid sulfate soils and other recent marine soils

Abstract

A refined scheme for the semi micro chemical analysis of sulfur fractions in soils is presented. Pyrite is analyzed, as iron, after extraction in HNO₃. Non‐pyrite iron is excluded by a pretreatment with HF/H₂SO₄. Water‐soluble sulfate and jarosite [KFe₃(SO₄)₂(OH)₆], the other dominant sulfur fractions in acid sulfate soils, are analyzed turbidimetrically, as sulfate, after successive extractions by EDTA.3Na (water soluble plus exchangeable SO₄) and by hot 4 M HCl (jarosite). These methods are simpler, less bulky and more specific than most existing procedures.

Introduction of elemental sulfur analysis permits estimation of organic sulfur fraction as well. Sums of individual sulfur fractions agree well with separate total sulfur determinations.

The proposed analysis of pyrite permits also distinction of the components Fe₂O₃, FeO and FeS₂ in soils and rocks².     

Response of acid sulphate soils to different liming treatments I. Solubility of sulphate and phosphate

In a preliminary laboratory experiment, samples from three cultivated and three virgin acid sulphate soils (pH 3.9-4.7) were treated with water or equivalent amounts of Ca(OH)₂ or KOH and incubated at about field capacity for three months. Both base treatments (133 meq/kg) similary reduced soil acidity and, thus, the same influence on the pH-dependent biological and chemical reactions was concluded. The liming-induced mineralization of organic S seemed to account for increased extratability of sulphate, being in most soils of the same magnitude in both treatments. Inversely, the solubility of P hardly was affected by the decomposition of organic matter but rather by the reactions of inorganic P. KOH markedly raised water-soluble P, whereas Ca(OH)₂ did not. The results of a rapid extraction test suggested that the poorer extractability of P in the soils amended with Ca(OH)₂ could partly be ascribed to a higher Ca saturation and its impact on the electrochemical properties of charged surfaces. In addition, a higher base-associated ionic strength created by Ca²⁺ was of great importance in reducing the P desorption in the Ca(OH)₂- treated soils.