腐殖质对白浆土中Fe、Mn、Al形态转化及磷生物有效性的影响

在三江平原布置长期试验，研究连年施用有机肥后土壤腐殖质变化及其对白浆±Fe、Mn、Al形态转化及磷生物有效性的影响。结果表明，施用牛粪后土壤腐殖质含量升高，且以松结态腐殖质的增长为主；土壤的DTPA提取态和有机络合态Fe、Mn、Al含量上升，使土壤有效态磷含量上升。因此，生物措施是治理白浆土，促进土壤磷素养分有效性上升，增大土壤缓冲容量和抗逆性的有效措施。     

甘肃主要农业土壤中Cu、Zn、Mn、Fe的形态及有效性研究

本文对甘肃省主要农业土壤中Ｃｕ、Ｚｎ、Ｍｎ、Ｆｅ的形态及其有效性进行了研究。结果表明，供试土壤的全Ｃｕ含量范围为２２－２４ｍｇ／ｋｇ，全Ｍｎ为５４２－７７２ｍｇ／ｋｇ，全Ｆｅ为３５６８５－３８３５５ｍｇ／ｋｇ。四种元素均以灌漠土的含量最低，褐土最高。土壤中Ｃｕ、Ｚｎ、Ｍｎ、Ｆｅ的大部分以残留矿物态和氧化铁结合态存在。生物试验和统计分析表明，Ｃｕ、Ｚｎ、Ｍｎ、Ｆｅ的交换态和松结有机态对植物最为有效，     

纳米TiO2对土壤Hg2+吸附解吸性能的影响

为了研究纳米TiO_2对土壤吸附解吸汞性能的影响,以三峡水库消落区土壤为代表,选择2种晶型(锐钛矿和金红石)的纳米TiO_2颗粒,设置3个浓度梯度(2,4,8g/kg),制成含有不同浓度纳米TiO_2颗粒的土样,配制不同浓度的Hg~(2+)溶液,进行吸附解吸试验。结果表明:纳米TiO_2颗粒可提高土壤对Hg~(2+)的吸附量,但受颗粒的晶型和浓度的影响;锐钛矿颗粒对土壤吸附解吸Hg~(2+)的影响更大,其吸附作用力更强,不易解吸,其中4g/kg处理组吸附作用最强,与对照相比,最大吸附量可提高32.65%,且其解吸率低于对照组;金红石颗粒处理组对Hg~(2+)的吸附量随颗粒浓度的升高而增大,但吸附作用力较弱,容易被解吸,8g/kg处理组影响最大,与对照相比,最大吸附量提高18.18%,但其解吸率也最大。因此,纳米TiO_2颗粒增强土壤对汞的吸附作用,从而可能影响汞在环境中的迁移转化过程,特别是锐钛矿型颗粒。     

我国酸性硫酸盐土壤中铁锰形态转化及迁移

酸性硫酸盐土壤酸性很强，有机质含量高，造成了这种土壤所特有的铁锰淋洗、转化和迁移规律。研究结果表明：在酸性硫酸盐土壤中全铁含量较低，一般在３５－５０ｇ／ｋｇ（以Ｆｅ２Ｏ３计），全锰含量也低，一般在０．２５－０．５５ｇ／ｋｇ（以ＭｎＯ计），一般滩涂中全铁大于６０ｇ／ｋｇ，全锰大于１ｇ／ｋｇ。酸性硫酸盐土壤中，铁的游离度较小，一般在３７－７０％，铁的活化度较大，一般在８－２０％，而滩涂中铁的游离度一般     

长期定位施肥对土壤铁、锰形态及剖面分布的影响

本文采用改进的BCR连续提取法,对沈阳农业大学棕壤肥料长期定位试验地31年不同施肥处理土壤铁和锰含量变化及其剖面变异规律进行研究。结果表明:与试验前相比,耕层土壤两种元素水溶态和弱酸溶态含量都有所增加,而可还原态和残渣态含量则有不同程度的减少;铁和锰都以残渣态和可还原态为主。在空间分布上,两种元素弱酸溶态和可氧化态含量随土层的加深而减少,残渣态则相反。研究表明,有机肥能在一定程度上改变铁和锰在各形态间的分配,并且有机肥能活化残渣态铁和锰。     

酸化及施碳酸钙对土壤各形态锰的影响

以灰潮土为对照 ,研究了华中地区 3种已明显发生酸化的土壤在施用碳酸钙前后各形态锰的变化情况。结果表明 ,已酸化的红壤、棕红壤和黄褐土施用碳酸钙降低了土壤酸度 ,土壤交换态锰随 pH值上升而降低 ,其降幅分别为 42 % ,49%和 39% ;其它形态锰的增减随各土而异 ,残留态锰较稳定 ,变幅小。作为对照 ,灰潮土虽与前 3种已酸化土壤一样种植过多茬作物 ,但其交换态锰含量仍甚微。无论是否施用碳酸钙 ,在灰潮土的交换态锰、碳酸钙结合态锰和易还原态锰 3种形态锰中 ,易还原态锰占 80 %以上 ,说明易还原态锰是其活性锰的主要部分     

土壤中植物有效锰的形态分级

用４种方法测定土壤有效态锰含量,并加以比较和评价,从而确定出最优的土壤有效锰测定方法。研究结果表明,采用一种顺序浸提的方法能比较准确地反映土壤的供锰状况,锰组分及其相应浸提剂为：易溶态锰（０．０５ｍｌ／ＬＣａ（ＮＯ３）２）提取、弱吸附态锰（ｐＨ８．５,ＣａＤＴＰＡ－Ｂ４Ｏ７）、碳酸盐束缚态锰（石灰性土壤,用１．６ｍｏｌ／ＬＨＮＯ３快速浸提）或专性吸附态锰（非石灰性土壤,用１．６ｍｏｌ／ＬＨＮＯ３快速浸提）或专性吸附态锰（非石灰性土壤,ｐＨ４．４,０．０５ｍｏｌ／ＬＣａ（ＮＯ３）２＋０．０５ｍｏｌ／ＬＣｕ（ＮＯ３）２提取）和氧化锰（ｐＨ２．０,０．１ｍｏｌ／ＬＮＨ２ＯＨ．ＨＣｌ）。由盆栽试验辣椒吸收的锰与土壤锰相关分析结果显示,易溶态锰是植物最易吸收的锰,其回归方程为：Ｙ＝－１４．４０９＋２１．６５８Ｘ,ｒ＝０．     

纳米TiO2催化下表层土壤中BaP的紫外光降解

采用光解试验,研究了紫外照射与纳米TiO2联合作用下,土壤表层中苯并[a]芘（BaP）的降解动力学;同时考察了催化剂的浓度、土壤pH、腐植酸和光质对BaP的光催化降解的影响。结果表明,土壤中BaP的光催化降解表现为准一级动力学。催化剂TiO2可以明显地促进土壤中BaP的光降解,较少量的催化剂（0．5％）使光解的半衰期从363．22h减少到103．26h。H^＋和OH^-离子对BaP的催化光解起促进作用,在酸性和碱性土壤中BaP光催化降解高于中性土壤,酸性土壤中的降解速率最快。腐殖质吸收紫外光照射时,产生的活性氧中间产物能够攻击BaP,添加腐植酸能增加土壤表层中BaP的光催化降解。BaP的光解半衰期从无外加腐植酸的89．34h,减少到添加浓度分别为5、10、20和40mg·kg^-1的29．37、32．69、35．73和38．51h。BaP的催化降解随波长的增加而降低,在波长254、310和365nm下,BaP降解的一级动力学常数分别为0．0078h^-1、0．0061h。和0．005h^-1。     

Waterlogging Induces High to Toxic Concentrations of Iron,Aluminum, and Manganese in Wheat Varieties on Acidic Soil

Six wheat varieties with different tolerance to waterlogging were studied in acidic soil (pH 4.5), neutral soil, and potting mix (pH 6.7–7.8) under controlled conditions. Waterlogging for 49 d reduced shoot dry weight by 48% to 85% compared with drained treatments. The ranking of varieties for waterlogging changed under different soils, and this change explains why waterlogging tolerance of these varieties may vary in different environments. In waterlogged acidic soil, shoot concentrations of aluminum (Al), manganese (Mn), and iron (Fe) increased by two- to 10-fold, and in some varieties they were above critical concentrations compared with plants in drained soil. These elements decreased or remained the same in shoots of plants grown in waterlogged neutral soil. Marginal nitrogen (N) deficiency was induced in most varieties in all soil types. The results support the importance of screening in soils from the target environment for accurate germplasm characterization for waterlogging tolerance.     

Effects of H2SO4 and HNO3 on Soil Acidification and Aluminum Speciation in Variable and Constant Charge Soils

The difference in effect on acidification and species of aluminum speciation between HNO₃ and H₂SO₄for two contrasting types of soils in surface charge was investigated. The results show that the effect of H₂SO₄ on acidification of variable charge soils (Ferric Acrisol and Haplic Acrisol) of subtropical regions wasweaker than that of HNO₃, due to the specific adsorption of SO₄ ^2- and the accompanied release of OH^-. For two constant charge soils, Haplic Luvisol andEutric Cambisol, the difference in effect between the two acids is small. The concentrations of total inorganic monomeric aluminum, Al³⁺, Al-F complexes and Al-SO₄complexes in the extract from variable charge soils are alsolower in H₂SO₄ systems than those in HNO₃ systems, whereas the reverse is true for constant charge soils, except the concentration of Al³⁺. For variable charge soils, Al-F complexes are the major species of inorganic monomeric aluminum at high pH butAl³⁺ might contribute to a largepart at low pH, while for constant charge soils Al-F complexes contribute almost exclusively to the inorganic monomeric aluminum. The presence of a large amount of SO₄ ^2- in the extract from the constant charge soilsleads to a higher proportion of Al-SO₄ complexes in totalinorganic monomeric aluminum than that from variable charge soil, although the numerical value of proportion is small.     

Interaction of Iron with Copper,Zinc, and Manganese in Wheat as Affected by Iron and Manganese in a Calcareous Soil

Iron (Fe) availability is low in calcareous soils of southern Iran. The chelate Fe-ethylenediamine di (o-hydroxy-phenylacetic acid) (Fe-EDDHA), has been used as an effective source of Fe in correcting Fe deficiency in such soils. In some cases, however, its application might cause nutritional disorder due to the antagonistic effect of Fe with other cationic micronutrients, in particular with manganese (Mn). A greenhouse experiment was conducted to evaluate the influence of soil and foliar applications of Fe and soil application of manganese (Mn) on dry matter yield (DMY) and the uptake of cationic micronutrients in wheat (Triticum aestivum L. var. Ghods) in a calcareous soil. Results showed that neither soil application of Fe-EDDHA nor foliar application of Fe sulfate had a significant effect on wheat DMY. In general, Fe application increased Fe uptake but decreased that of Mn, zinc (Zn), and copper (Cu). Application of Mn increased only Mn uptake and had no significant effect on the uptake of the other cationic micronutrients. Iron treatments considerably increased the ratio of Fe to Mn, Zn, Cu, and (Mn + Zn + Cu). Failure to observe an increase in wheat DMY following Fe application is attributed to the antagonistic effect of Fe with Mn, Zn, and Cu and hence, imbalance in Fe to (Mn + Zn + Cu) ratio. Due to the nutritional disorder and imbalance, it appears that neither soil application of Fe-EDDHA nor foliar application of Fe-sulfate is appropriate in correcting Fe deficiency in wheat grown on calcareous soils. Hence, growing Fe-efficient wheat cultivars should be considered as an appropriate practice for Fe chlorosis-prone calcareous soils of southern Iran.     

植物多酚与低分子量有机酸联合作用对紫色土铁形态分布的影响

植物多酚(PP)和低分子量有机酸(LMWOA)对土壤铁形态转化有重要影响。以酸性、中性和石灰性紫色土为研究对象,采用不完全随机区组试验,用2种PP(即表没食子儿茶素没食子酸酯(EGCG)和芦丁)和2种LMWOA(即柠檬酸和草酸)溶液浸提供试土壤,测定其可溶铁(Fes)、游离铁(Fed)、活性铁(Feo)、络合铁(Fep)含量,探讨了PP与LMWOA对紫色土铁形态分布的影响。结果表明:PP与LMWOA各自单独作用均能使酸性紫色土Fes增加、中性紫色土Fes减少;对于石灰性紫色土,PP会促进其Fes增加,而LMWOA作用相反。EGCG与LMWOA联合作用,在酸性和石灰性紫色土上均表现为LMWOA通过促使本应转化为Fes的转化为Fep而掩蔽EGCG对铁的溶解作用;芦丁与LMWOA联合作用,在酸性紫色土铁的溶解上表现为协同效应,在石灰性紫色土上则表现为LMWOA会抑制芦丁对铁的溶解作用;对于中性紫色土,PP与LMWOA联合作用可促进Fed向Fes转化而削弱PP对铁溶解的抑制作用。     

Predicting Liming Needs of Soybean Using Soil pH,Aluminum, and Manganese Soil Tests

Abstract

Whether a tropical soil should be limed or not for a particular crop is strongly dependent on the levels of soil aluminum (Al) which can be determined with soil tests. Soil pH is used to predict whether lime is needed in less‐weathered soils, although some evidence indicates a soil Al test would be more accurate. The objectives of this study were to determine and to compare the accuracies of four soil tests to separate soils requiring lime from those that do not, and to determine the cause of acid‐soil injury to soybean [Glycine max (L.) Merr.]. Soybean was grown in the greenhouse on four surface soils representing the major land resource areas of Louisiana and were amended with eight rates of lime, yields determined, and soils analyzed for soil pH, extractable Al, CaCl₂‐extractable Al, CaCl₂‐extractable manganese (Mn), and Al saturation. Acid‐soil injury in soybean grown on the Litro clay and Stough fsl was probably caused by soil‐Al effects while low soil calcium (Ca) and high soil Mn was likely responsible for lower yields from the Mahan fsl. Leaf Ca from the limed Mahan‐soil treatment was 5‐fold greater and leaf‐Mn 7‐fold less than control levels. Regression analyses’ R² values were similar for all soil tests except for CaCl₂‐extractable Mn, which was lower. Soil tests were compared across soil type by selecting treatments that had the same 85% relative yield. Using this data subset, there was no difference in the soil pH among the four soils, while there were significant differences among soils for all other soil test measurements indicating the superiority of soil pH for identifying acid‐soil injury. Critical test values were 5.1 soil pH, 30 mg kg^‐1 extractable Al, 7% Al saturation, 0.7 mg‐kg^‐1 CaCl₂‐extractable Al, and 9 mg‐kg^‐1 CaCl₂‐extractable Mn.     

The Influence of Pedology and Changes in Soil Moisture Status on Manganese Release from Upland Catchments: Soil Core Laboratory Experiments

Manganese (Mn) contamination of drinking water may cause aesthetic and human health problems when concentrations exceed 50 and 500 μg l^?1, respectively. In the UK, the majority of Mn-related drinking water supply failures originate from unpolluted upland catchments. The source of Mn is therefore soil, but the exact mechanisms by which it is mobilised into surface waters remain unknown. Elevated Mn concentrations in surface waters have been associated with the rewetting of dried upland soils and with conifer afforestation. We investigated these hypotheses in a laboratory experiment involving the drying and rewetting of intact soil cores (1,900 cm³ volume) of horizons of four representative soil type-land use combinations from an upland water supply catchment in southwest Scotland. Although no statistically significant effect of land use or soil type was detected on Mn concentrations in soil water, Mn release occurred from three soil horizons upon rewetting. Soil water Mn concentrations in the moorland histosol H2 (10–30 cm), the histic podzol H and Eh horizons increased from means of 5.8, 6.2 and 0.6 μg l^?1 prior to rewetting to maxima of 90, 76 and 174 μg l^?1 after rewetting, respectively. The properties of these three horizons indicate that Mn release is favoured from soil horizons containing a mixture of organic and mineral material. Mineral material provides a source of Mn, but relatively high soil organic matter content is required to facilitate mobilisation. The results can be used alongside soil information to identify catchments at risk of elevated Mn concentrations in water supplies.     

Kinetics of Iron and Manganese Release from Contaminated Calcareous Soils

Knowledge of the release of heavy metals (HM) and their chemical speciation is necessary for characterizing HM behavior in soils. The kinetics and characteristics of iron (Fe) and manganese (Mn) release were studied in 10 contaminated calcareous soils using 0.01 M calcium chloride (CaCl₂), 0.01 M ethylenediamine tetraacetic acid (EDTA), and 0.01 M malic acid (malic acid) extractions. Iron and Mn in soil samples were fractionated before and after 2084 h kinetic release using a sequential extraction procedure. The proportion of Fe and Mn released by EDTA was greater than that with CaCl₂ and malic acid. A power model satisfactorily described Fe and Mn release from soils. In general, the mean release rate of Fe was greater than that of Mn, indicating a greater rate of Fe release from contaminated soils. It was shown that Fe and Mn distributions were similar in native soils and they were mainly found in Fe-Mn oxides and organic-matter (OM) fractions. There were changes in the proportional distribution of Fe and Mn in all soils during the 2084 h kinetic study with different extraction solutions. In general, the proportions of Fe and Mn associated with carbonate (CARB) and OM fractions tended to decrease, with corresponding increases in the Fe-Mn oxides for Mn and residual (RES) fractions for Fe during the kinetic study with all extraction solutions. The Fe and Mn solubility at the initial and final stages of release was controlled by siderite (FeCO₃), vivianite [(Fe)₃(PO₄)₂·8H₂O], MnCO₃(am), MnHPO₄, and rhodochrosite (MnCO₃) minerals in all extraction solutions. Based on a risk assessment and percentage of release of metals, there is a high potential for Mn release into the food chain from contaminated soils.     

Changes in Fractions of Iron,Manganese, Copper,and Zinc in Soil under Continuous Cropping for More Than Three Decades

The effect of continuous cropping with maize and wheat on soil characteristics and various forms of micronutrient cations in an Incetisol over the years was studied in an ongoing long‐term experiment in New Delhi, India. The soil samples collected in the years of 1993, 1995, 1997, 1999, 2001, 2003, and 2004 were analyzed for different fractions of iron (Fe), manganese (Mn), copper (Cu), and zinc (Zn) by following a sequential extraction procedure. The pH, electrical conductivity (EC), and calcium carbonate (CaCO₃) content of the soil varied from 8.28 to 8.53, 0.40 to 0.43 dSm^?1, and 0.92 to 1.05%, respectively. Organic carbon content ranged from 0.38 in the control to 0.67% in 100% NPK + farmyard manure (FYM). Diethylenetriaminepentaacetic acid (DTPA)–extractable Fe and Mn (but not Zn and Cu) in soil declined from their respective initial (1971) values as a result of intensive cropping for more than three decades. It also resulted in a decrease in the concentrations of all the four metallic cations bound to organic matter, in addition to Fe and Zn, associated with carbonates in all the treatments in surface soil.     

采煤塌陷区土壤磷赋存形态及其释放规律

[目的]对采煤塌陷区土壤中磷赋存形态以及释放规律进行研究,了解土壤磷污染特征。[方法]以淮南矿区潘一矿塌陷区为研究对象,应用分级提取的方法对塌陷区土壤中磷的赋存形态进行分析测定,采用室内柱状样模拟实验对土壤中磷释放特征进行研究。[结果](1)潘一杨庄塌陷区土壤TP的含量在103.58~489.89 mg/kg之间,平均值为248.47 mg/kg;(2)活性磷(BAP)的含量在86.94~378.24mg/kg,占TP含量的43.53%~91.12%,平均为71.1%。(3)TP累计释放量大小依次为:pH=12pH=3pH=6pH=8pH=10pH=4。[结论]采煤塌陷区土壤中TP有极高的释磷潜力;不同pH值条件下,磷的释放强度大小为:碱性酸性中性。     

不同污染区土壤汞的分布特征及变化规律

为揭示不同污染区重金属汞在土壤中的存在形态及分布特征,选取万山汞矿区、大龙燃煤电厂区为研究区域,以无污染区花溪区为对照,选择优化的Tessier连续化学浸提法进行汞的形态分析。结果表明:万山汞矿区与大龙燃煤电厂的土壤总汞平均值分别为22.7 mg/kg和0.648 mg/kg,均超过我国土壤环境质量二级标准(0.5 mg/kg),无污染对照区土壤总汞平均为0.179 mg/kg。在水平方向上,万山汞矿区靠近污染源的土壤汞含量相对较高,随着距离的增加而下降;大龙燃煤电厂区土壤汞在距燃煤电厂2.5 km范围内呈现先减小后增大的趋势。汞矿区土壤汞主要以残渣态(66.6%)为主,其次为有机结合态(30.0%);燃煤电厂则主要以有机结合态(75.7%)为主,其次为残渣态(17.46%);无污染区主要以残渣态(59.1%)为主,其次为有机结合态(28.9%)。内梅罗污染综合指数显示,万山汞矿区的土壤污染指数为107,为重度污染,这与污染源强度大有关,2004—2017年,总汞含量呈下降趋势;大龙燃煤电厂土壤污染指数为1.57,为轻度污染,同时土壤汞以有机结合态为主,潜在生物有效性相对较高,有一定的...