酸性硫酸盐土酸消长的水动力机制研究

以不同土壤湿度、不同干湿交替周期和原状土自然风干 8个处理进行酸性硫酸盐土 (简称ASS)室内模拟实验。通过对模拟过程内土壤pH、总硫化物性酸度和未氧化双氧水可氧化硫、交换性酸度、硫派生的实际酸度、KCl可提取硫等指标的动态变化过程的跟踪测定和分析显示 ,土壤水分条件是制约ASS酸度及酸形态转化的重要动力机制 ,可导致ASS酸度和酸形态的有规律变化。ASS产酸量和洗酸量受干湿交替周期制约     

稻作对酸性硫酸盐土酸分布及迁移的影响

【目的】酸性硫酸盐土(ASS)酸含量极高,Fe、 Al、 Mn、 As等有毒金属移动性强。许多开发利用方式不仅影响其成土母质黄铁矿的氧化程度并可能带来生态风险,稻作利用被认为是生态风险较低的方式。本研究开展水田和荒地两种利用条件下ASS中酸含量调查研究,探讨稻作利用方式对ASS酸含量的影响。【方法】于2013年8月,在广东省台山市发育于珠江三角洲滨海ASS的水稻田和严重酸化的长期撂荒地采集土壤样品,从土表向下0—300 cm范围内采用宽45 mm的土钻每20 cm采集1个样品,每个剖面共采集15个样品。比较两种利用方式下ASS各土层土壤pH值、 水溶性酸、 交换性酸、 吸持性酸含量,探讨稻作利用方式对ASS酸分布及运移的影响。【结果】珠江三角洲平原ASS的酸含量极高,在0—80 cm深度范围内,总存在酸含量随着土层深度加深而提高,土层深度每下降20 cm,总存在酸含量就平均提高61.62%; 80 cm以下土层总存在酸含量随着土层深度下降逐渐降低,其中80—180 cm深度范围内的降幅较大,土层深度每下降20 cm,总存在酸含量就平均降低61.62%; 当土层深度下降至220 cm时,pH值上升到6.0,酸含量非常低。稻作利用方式显著影响ASS的酸含量及其在土壤剖面的迁移情况。与荒地比较,稻田0—80 cm土层的总存在酸含量显著降低,其中水溶性酸、 交换性酸和吸持性酸含量平均降幅分别为77.01%、 36.75%、 27.74%,水溶性酸和交换性酸的差异达到显著水平,吸持性酸仅在0—20 cm 和60—80 cm土层的差异达到显著水平; 100—120 cm深度范围内稻田的总存在酸含量显著高于荒地,其中水溶性酸、 交换性酸和吸持性酸含量的增幅分别为128.19%、 54.87%、 154.96%,120—240 cm土层中,稻田的交换性酸和吸持性酸含量稍高于荒地,但差异不显著; 240—300 cm土层中,稻田的酸含量与荒地基本相同。总体上,稻作方式改变了ASS中酸在土壤剖面的分布,其中0—80 cm土层中酸含量显著降低,而100—120 cm土层的酸含量显著提高,并以吸持性酸为主要形式固定累积下来。稻田在0—80 cm深度范围内的水溶性硫含量显著低于荒地; 而稻田100—120 cm土层的水溶性硫含量则显著高于荒地,其他土层的差异不显著。水溶性硫与水溶性酸、 交换性酸和吸持性酸均显著正相关,表明稻作利用方式可能通过影响硫酸盐矿物的转化过程而改变ASS的酸分布及迁移。【结论】稻作利用方式显著降低上层土壤酸含量,并加强了酸淋洗下移作用,使100—120 cm土层中的酸含量大幅提高,并以黄钾铁矾等羟基硫酸盐次生矿物暂时吸持固定下来。因此,稻作利用方式有效降低ASS酸含量水平,降低ASS对实地作物的危害作用,但因其强淋溶作用可能加大了对地下水体污染的风险。     

南方茶园土壤酸化特征及交换性酸在水稳性团聚体中的分布

通过采集浙江省杭州西湖龙井茶园土壤,研究茶园土壤剖面的酸度特征、养分变化以及交换性酸在水稳性团聚体中的分布特征,以了解南方茶园土壤的酸化过程。结果表明:茶园表层土壤(0-20cm)酸化严重,最低的pHH2O值达到4.0,并且有明显的深层化趋势;表土的有机质和速效磷含量较高,速效磷含量最高可达138.2mg/kg;表土团聚体分级表明茶园土壤有良好的团聚体结构,具有良好的水稳性;除了交换性H+在0.5～0.25mm和0.25～0.106mm水稳性团聚体之间没有明显差别外,交换性酸总量、交换性H+和交换性Al 3+含量均随着水稳性团聚体粒径的减小而降低;水稳性大团聚体中交换性Al 3+相对交换性H+占有明显的优势,而在0.106～0.05mm水稳性微团聚体中交换性H+占有明显的优势。交换性酸总量、交换性H+和交换性铝主要分布于>2mm和2～0.5mm水稳性团聚体中,同时在不同粒级团聚体中的分布随粒径的减小而降低。     

在实验酸性硫酸盐条件和酸性硫酸盐土壤上可溶性铝的控制

The controls of soluble Al concentration were examined in three situations of acid sulfate conditions:1) experimental acid sulfate conditions by addition of varying amounts of Al(OH)3(gibbsite) into a sequence of H2SO4 solutions;2)experimental acid sulfate conditions by addition of the same sequence of H2SO4 solutions into two non-cid sulfacte soil samples with known amounts of acid oxalate extractable Al; and 3) actual acid sulfate soil conditions.The experiment using gibbsite as an Al-bearing mineral showed that increase in the concentration of H2SO4 solution increased the soluble Al concentration,accompanied by a decrease i the solution pH, Increasing amount of gibbsite added to the H2SO4 solutions also increased soluble Al concentration,but resulted in an increase in solution pH.Within the H2SO4 concentration range of 0.0005-0.5mol L^-1 and the Al(OH)3 range of 0.01-0.5g(in 25 mL of H2SO4 solutions),the input of H2SO4 had the major control on soluble Al Concentration and pH .The availability of Al(OH)3,however,was responsible for the spread fo the various sample points,with a tendency that the samples containing more gibbsite had a higher soluble Al concentration than those containing less gibbsite at equivalent pH levels.The experimental results from treatment of soil samples with H2SO4 solutions and the analytical results of acid sulfate soils also showed the similar trend.     

碱性材料对修复与改良酸性硫酸盐土壤障碍因子的研究

采用盆栽试验研究了不同碱性材料(石灰、自研改良剂、钙镁磷肥)对酸性硫酸盐土壤主要障碍因子的修复及其对水稻生长的影响。结果表明,不同碱性材料对土壤理化特性、土壤养分有效性和水稻生长的影响存在明显差异。与常规施肥(NPK)处理相比,自研改良剂(SAM)和钙镁磷肥(CMP1)处理土壤p H增加了1.25和0.92个单位,土壤速效磷含量分别增加了3.1倍和2.6倍,土壤有效铁、有效锰、交换性H+、Al3+含量均大幅下降。SAM与CMP1处理通过提供足够的有效磷并补充钙、镁等元素,有效改善了根系生长环境,从而有效控制铁、锰、铝等元素向地上部转运,进而对作物的生长起到促进作用。SAM和CMP1处理较NPK处理有效促进了关键生育期水稻根系活力并显著增加了水稻籽粒产量,增幅分别达121.1%和105.1%。石灰效果次之。综上,初步认为碱性材料改良酸性硫酸盐土壤的关键在于保证了充足有效磷的同时,提高了土壤p H,降低了土壤金属的毒害。本试验条件下,钙镁磷肥对修复和改良酸性硫酸盐土壤障碍因子效果非常明显,但其成本是自研改良剂的3倍,因此,基于改良剂的成本与长期适用性考虑,自研改良剂可能是该类土壤改良的最佳选择。     

铁观音茶园土壤酸化与交换性镁的现状

明确了酸化茶园中的土壤交换性镁状况,为茶园科学施肥提供支持.在安溪县主要产茶乡镇共采集了297个表层土壤样品,通过测定土壤pH及土壤交换性镁含量,应用描述性统计分析进行了分布特征研究,应用相关分析进行了土壤pH与交换性镁相关性研究.安溪茶区的土壤pH值变幅在3.1～6.7之间,超过68％的茶园土壤pH低于4.5,土壤酸...     

不同酸性物质对石灰性土壤的酸化效果研究

采用室内模拟试验研究了酸性物质对石灰性土壤的酸化效果。结果表明,磷酸能有效地降低石灰性土壤的pH,要使土壤pH由8.89降至6.0左右,最佳酸用量为3.27g/100g土。对于pH较高的石灰性土壤,只用低pH(pH=5.5)的酸水溶液在短时间内降低土壤pH是不切实际的。磷酸二氢铵不仅具有很好的酸化效果,且具有很好的缓冲性能,每100g土壤加入2.3g磷酸二氢铵可使石灰性土壤pH从8.89降低到6.39,并能维持较长的酸性环境。施用5%的硫磺可在30d内使土壤pH降低到7.0～7.5之间。     

不同提取剂连续提取下某酸性硫酸盐土壤酸的释放

An acid sulfate soil sample was successively extracted with deionized water,1 molL^-1 KCl and 0.0005mol L^-1 Ca(OH)2 solutions.The results showed that only very small amounts of acidity were extracted by deionized water,possibly through slow jarosite hydrolysis.Acid release through jarosite hydrolysis was greatly enhanced by Ca(OH)2 extraction at the expense of the added OH^- being neutralized by the acid released.Successive extration of the sample with KCl removed the largest amounts of acidity from the sample.However,it is likely that the major form of acidity released by KCl extraction was exchangeable acidity.The results also show the occurrence of low or non charged Al and Fe species in water and Ca(OH)2 extracts after first a few extractions .It appears that such a phenomenon was related to a decreasing EC value with increasing number of extractions.     

The effect of lime levels on the growth of beans and maize and nodulation of beans in three tropical acid soils

Abstract

A study to investigate the effect of lime on dry matter yield of maize (Zea mays) and beans (Phaseolus vulgaris) and nodulation of beans grown in three tropical acid soils (two humic Nitosols and one humic Andosol) was carried out in a greenhouse. The soils ranged from 4.2 to 5.0 in pH; 1.74 to 4.56 in %C; 21.0 to 32.0 meq/100g in CEC; 5.10 to 8.10 meq/100g in exchange acidity; 0.60 to 3.20 meq/100g in exchangeable (exch.) Al and 0.13 to 0.67 meq/ 100g in exch. Mn.

Exchange acidity and exch. Al decreased with increasing levels of lime in the three soils. Exchangeable Al was reduced to virtually zero at pH 5.5 even in the soils which had appreciable initial amounts. Exchangeable Mn also decreased with increasing levels of lime in the two Nitolsos. Exceptional results, however, were obtained with the Andosol where exch. Mn increased ten‐fold with the first level of lime and then decreased with subsequent levels.

In all the soils, mean dry matter yield of beans and maize, and mean nodule dry weight of beans generally increased significantly with increasing lime levels up to pH value of 6.0. The dry matter yield of beans and maize, and nodule weight of beans, however, decreased progressively with increasing lime levels beyond pH 6.0 value. pH range of 5.5 to 6.0 was considered optimum for the growth of maize and beans, and nodulation of beans in these soils.     

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.     

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.     

Extraction of potassium from some kaolinitic soils of the tropics

Abstract

Three methods for soil potassium extraction (M NH₄OAc pH 7, 0.01 M AgTU and 30 % hot H₂SO₄) were compared for a variety of kaolinitic soils of the tropics. The AgTU‐extractable K was much higher than the M NH₄OAc‐extractable K when vermiculite clay was present in the soil. The correlation between both was given by an R value of 0.937. The amounts of K extracted by 0.01 M AgTU and by hot H₂SO₄ were approximately the same. The R value for these two methods was 0.843.

It is suggested that the AgTU extractant could be used for determination of plant‐available K in soil and for testing for the presence or absence of vermiculite clay in soils.     

Nutrient Element Contents and Cation Exchange Capacity in Fine Fractions of Southeastern Nigerian Soils in Relation to Their Stability

Abstract

Soils collected from 15 locations from SE Nigeria at the 0‐ to 20‐cm depth were studied for the nutrient elements of fine fractions and their role in the stability of the soils. The objective was to understand the role of these elements in the stability of the aggregates. The fine fractions were clay and silt, and elements measured in the fine fractions were exchangeable sodium (Na⁺), potassium (K⁺), calcium (Ca²⁺), magnesium (Mg²⁺), exchangeable acidity (EA), cation exchange capacity (CEC), and available phosphorus (P). The aggregate stability was measured at the microlevel with clay dispersible indices and water‐stable aggregate (WSA) <0.25 mm, and at macrolevel with other WSA indices and mean‐weight diameter (MWD). Soils varied from loamy sand to sandy clay. There were more exchangeable cations, CEC, EA, and available P in clay than in the silt fraction. Whereas EA values ranged from 2.8 to 10.4 cmol kg^?1, they were between 1.6 and 9.2 cmol kg^?1 in silt. The CEC in the clay fraction was from 7.4 to 70 cmol kg^?1 and between 4.0 and 32.8 cmol kg^?1 in the silt fraction. The WDC were from 50 to 310 g kg^?1 while the average dispersion ratio (DR) was generally higher than the corresponding clay‐dispersion ratio (CDR), and the MWD ranged from 0.45 to 2.68 mm. Soils with WSA skewed mostly to higher WSA (>2–1.00 mm) had a higher MWD. Exchangeable Ca²⁺ in clay correlated significantly with CDR and WSA sizes 1.0–0.5 mm and 0.5–0.25 mm (r=0.45,* 0.51,* and 0.60*), respectively, but negatively correlated with clay flocculation index (CFI) (r=?0.45*). Also, available P in clay correlated respectively with CDR and CFI (r=0.45*, ?0.45*), whereas K⁺ in silt correlated significantly with WDSi (r=0.64*), CFI (r=0.62*), and CDR (r=?0.65*). Principal component analysis revealed that elemental contents in the silt fraction can play very significant roles in the microaggregate stability.     

玉米秸秆和Al2(SO4)3对苏打盐碱土主要盐碱化指标的影响

采用室内培养试验研究添加玉米秸秆和Al2(SO4)3对苏打盐碱土pH值、可溶性盐含量和阳离子交换量的影响,旨在为盐碱土合理改良利用提供理论依据。研究发现,加入玉米秸秆和Al2(SO4)3后,苏打盐碱土pH值有不同程度的降低。当Al2(SO4)3加入量为0%～0.8%时,随着Al2(SO4)3加入量的增加,苏打盐碱土pH值急剧下降,而当Al2(SO4)3加入量继续增加时,则pH值变化较缓慢。Al2(SO4)3加入量相同时,玉米秸秆的添加对降低苏打盐碱土的pH值具有略微促进的作用。在玉米秸秆和Al2(SO4)3的共同作用下,苏打盐碱土Na+、K+、Ca2+和Mg2+的含量均升高,而CO32-和HCO3-的含量则随着玉米秸秆和Al2(SO4)3加入量的增加而逐渐降低。玉米秸秆和Al2(SO4)3的加入使苏打盐碱土的阳离子交换量也有所增加,阳离子与土壤胶体上的Na+进行置换,最终使苏打盐碱土碱化度下降。综合而言,试验条件下,15%玉米秸秆和0.8%Al2(SO4)3对苏打盐碱土的改良效果最佳。