反射光谱估算滨海土壤黏粒含量

探明反射光谱估算土壤黏粒含量的成因是实现黏粒含量测定、提高估算精度的基础。该文以江苏省滨海平原的150个土壤样品为研究对象,将测得的原始光谱数据进行平滑、一阶导数、连续统去除和倒数等数据变换,采用逐步多元线性回归(stepwise multiple linear regression,SMLR)和偏最小二乘回归(partial least squares regression,PLSR)方法估算黏粒含量,并在此基础上分析建模的影响波段,探讨反射光谱估算土壤黏粒含量的成因。结果表明,连续统去除光谱数据的SMLR分析估算精度最高,建模集和验证集决定系数分别为0.941和0.750。360~900、1 800~2 490 nm是黏粒含量的重要建模影响波段,该建模影响波段主要包括铁离子(410 nm附近)、土壤有机质(500~800 nm)、层状硅酸盐中的结晶水(1 900 nm附近)、绿泥石和蛭石等黏土矿物(2 325 nm)的吸收特征波段;PLSR分析表明,1 400 nm附近回归系数出现的双峰特征源于高岭石的双峰吸收。黏粒中的黏土矿物、黏粒对铁离子的吸附特性以及黏粒与有机质的高度相关性是实现反射光谱估算滨海土壤黏粒含量的原因。     

有机酸对高岭石, 针铁矿和水铝英石吸附镉的影响

Effects of organic acids （oxalic, acetic, and citric） on adsorption characteristics of Cadmium （Cd） on soil clay minerals （kaolinite, goethite, and bayerite） were studied under different concentrations and different pH values. Although the types of organic acids and minerals were different, the effects of the organic acids on the adsorption of Cd on the minerals were similar, i.e., the amount of adsorbed Cd with an initial solution pH of 5.0 and initial Cd concentration of 35 mg L^-1 increased with increasing concentration of the organic acid in solution at lower concentrations, and decreased at higher concentrations. The percentage of Cd adsorbed on the minerals in the presence of the organic acids increased considerably with increasing pH of the solution. Meanwhile, different Cd adsorption in the presence of the organic acids, due to different properties on both organic acids and clay minerals, on kaolinite, goethite, or bayerite for different pHs or organic acid concentrations was found.     

A comparison between X‐ray fluorescence and dissolution methods employing lithium metaborate fusion for elemental analysis of soil clays

Abstract

A method employing fusion of soil clay samples with lithium metaborate (1:5 ratio) in a furnace at 1050°C for 1 hr. subsequent dissolution of the fused sample in 4% HNO₃. and elemental analysis for Si, Al, Fe, Ca, Mg, K, and Ti by atomic absorption spectrometry was compared with the X‐ray fluorescence (XRF) fused disc technique for analysis. Duplicated analyses were performed on 15 clay samples from soils of the southern U.S and three API reference samples. The mean total percent recovery by this method was excellent (100.14 ± 2.85). Elemental oxide quantities in terms of SiO₂. Al₂O₃, Fe₂O₃, MgO, CaO and K₂O determined by atomic absorption/flame emission (AA/FE) spectroscopy were in good agreement with values measured by x‐ray fluorescence (XRF) on the same subsamples (r = 0.89^* to 0.98^**). but somewhat more variable on subsamples seperated from different pretreatments (r = 0.70^* to 0.97^** ). The method, which has also been tested on 36 additional clay samples from a variety of Kentucky soils with total percent recoveries ranging from 96.5 ‐ 103.5%. demonstrated no bias due to mineralogy with respect to mixed, montmorillonitic. and siliceous classes. This technique presents numerous advantages over other elemental analysis techniques utilizing fusion, dissolution, or XRF spectroscopy with respect to time, effort and cost. With the introduction of inductively‐coupled plasma (ICP) emission spectroscopy. efficiency can be additionally improved.     

Bulk density by Proctor test as a function of texture for agricultural soils in Maputo province of Mozambique

Soil degradation processes may be of various kinds, including soil compaction. The present study was carried out with the objective of assessing the sensitivity of agricultural or recently abandoned soils in Maputo province of Mozambique to compaction. The assessment is based on the maximum of bulk density attained using the Proctor test (MBD).

In this study the soil texture is expressed by silt plus clay (S + C) or clay (C). The relations between the soil texture and MBD, and between soil texture and critical water content (CWC—soil water at which MBD is attained) were determined. Selected soils range from 10 to 74% of S + C and 9 to 60% of C.

The results suggest there is a relationship between the considered parameters, being that between S + C and MBD or CWC, the best. For MBD the relationship is represented by two quadratic equations with the boundary in between these being a S + C value of 25% and C value of 20%.

Based on the obtained results, one can conclude that the selected parameters may be a useful basis for estimation of the sensitivity to compaction of the Maputo province's soils. It is recommended that similar studies be carried out for soils under forest land and for soil of other provinces to establish the national physical degradation hazard as a function of soil parameters determined routinely and at low cost. The suggested parameters are texture and soil organic matter (SOM).     

Effects of Different Rates of Ca2+ Addition on Respiration and Sorption of Water-Extractable Organic C to a Vertisol Subsoil

It is well known that calcium (Ca²⁺) plays an important role in binding organic matter to clay. However, most previous studies were conducted with either topsoil or pure aluminosilicates. Less is known about the effect of Ca²⁺ on binding of organic matter to clay-rich subsoils, which have lower organic-matter contents than topsoils, and their clays are more strongly weathered than pure aluminosilicates. Two experiments were conducted with a Vertisol subsoil (69% clay): a laboratory incubation and a batch sorption. The mineral substrate in the incubation experiment was pure sand alone or sand amended with 300 g clay kg^?1. Powdered calcium sulfate (CaSO₄) at rates of 0, 5, 10, and 15 g Ca kg^?1 and mature wheat residue at a rate of 20 g kg^?1 were added to this mineral substrate and the water content was adjusted to 70% of water-holding capacity. Carbon dioxide release was measured for 28 days. Cumulative respiration per g soil organic carbon (C) (SOC from clay and residues) was increased by clay addition. Increasing Ca²⁺ addition rate decreased cumulative respiration in the sand with clay but had no effect on respiration in the pure sand. Clay and Ca²⁺ addition had no significant effect on microbial biomass carbon (MBC) per g SOC but clay addition reduced the concentration of potassium sulfate (K₂SO₄)–extractable C per g SOC. For the batch sorption experiment, the subsoil was mixed with 0 to 15 g Ca kg^?1 and water-extractable organic C (WEOC) derived from mature wheat straw was added at 0, 1485, 3267, and 5099 mg WEOC kg^?1. Increasing Ca²⁺ addition rate increased sorption of WEOC, particularly at the greatest concentration of WEOC added, and decreased desorption. This study confirmed the importance of Ca²⁺ in binding organic matter to clay and suggests that Ca²⁺ addition to clay-rich subsoils could be used to increase their organic C sequestration.     

Effect of humic acid on growth and crop nutrient status of wheat on two different soils

The effect of plant-derived humic acid (PDHA) and coal-derived humic acid (CDHA) on wheat growth was tested on two alkaline calcareous soils in pots. Humic acid derived from plant and coal materials was applied at the rate 0 (control), 50 and 100 kg/ha to wheat in pots carrying two soils viz. clayey loam soil and sandy loam soil separately. Data was collected on plant growth parameters such as spike weight, grain and straw weight, and plant nutrients (macronutrients and micronutrients). Results showed that spike weight increased by 19%, 15%, and 26%, and 11% with application of PDHA at the rate of 50 and 100 mg/kg in clayey loam and sandy loam soil, respectively. Grain yield show an increase of 21% and 11% over control with application of PDHA and CDHA at the rate of 50 mg/kg on both soils, respectively, and 10% and 22% with application of PDHA and CDHA at the rate of 100 mg/kg on both soils.     

华中黄棕壤和黄褐土粘粒胶膜的微量元素地球化学特征

The relationships between the basic properties and trace elementsin soil argillans and corresponding matrix soils were studied by sampling from the B horizons of 26 Alfisols in croplands of the subtropical area in Central China. The soil elements (K, Na, Ca, Mg, Mn, Co, Cu, Cr, Cd, Li, Mo, Ni, Pb, Ti, V, and Zn) were extracted by acid digestion and their contents were measured using inductively coupled plasma optical emission spectrometry (ICP-OES). The mean contents of clay and organic matter in the argillans were approximately 1.1 and 1.3 times greater than those in the matrix soils, respectively. The pH values and the contents of P₂O₅ and bases (K₂O, Na₂O, CaO, and MgO) in the argillans were higher than those in the corresponding matrix soils. Cu, Cd, Ti, and V were enriched in the argillans. Correlation coefficients and factor analyses showed that Co, Cu, Li, and Zn were bound with phyllosilicates and manganese oxides (Mn-oxides) in the argillans. Cr and Pb were mainly associated with iron oxides (Fe-oxides), while Ni was bound with Mn-oxides. Cd, Ti, and V were chiefly associated with phyllosilicates, but Cr and Mo were rarely enriched in the argillans. In contrast, in the matrix soils, Co and Zn were associated with organic matter and Fe-oxides, Cr existed in phyllosilicates, and Mo was bound to Fe-oxides. Cd, Ti, and V were associated with organic matter. The results of this study suggest that clays, organic matter, and minerals in the argillans dominate the illuviation of trace elements in Alfisols. Argillans might be the active interfaces of elemental exchange and nutrient supply in cropland soils in Central China.     

A gamma‐ray spectrometry approach to field separation of illuviation‐type WRB reference soil groups in northern Thailand

According to the World Reference Base for Soil Resources (IUSS Working Group WRB, 2006), the differentiation of Acrisols and Alisols is based on the cation‐exchange capacity of clay, which cannot be directly determined in the field, but needs expensive and time‐consuming soil‐chemical analyses. This is an unsatisfactory situation for pedologists, who urgently require a rapid field method to distinguish illuviation‐type reference soil groups (Alisols, Acrisols, Luvisols, Lixisols). In this study, we tested the ability of gamma‐ray spectrometry to separate major WRB reference soil groups in the field. The underlying hypothesis is that Alisols and Acrisols are distinguished by their clay mineral composition, which should be reflected by geochemistry and consequently gamma‐ray radiation (i.e., K‐containing illite vs. K‐free kaolinite). Highly significant differences in their gamma‐ray spectrum for K, Th, and U were found for limestone and its soils. Especially the K and Th signatures allowed a clear separation of Acrisols and Alisols. In general, the surface radiation was sufficient to separate these soils. Best results were revealed considering parent rock and the whole soil profile. This means by using a portable radiometer and a pH meter, all illuviation‐type reference soil groups could be distinguished in this case. If applicable at other sites, this approach could enormously reduce expenditures for soil‐chemical analysis needed to assist soil classification.     

Potassium behavior and clay mineral composition in the soil with low effectiveness of potassium application

ABSTRACT

Increasing exchangeable potassium (ExK) content in soil to an appropriate level is important to mitigate the transfer of radioactive cesium to crops. We focused on a buckwheat (Fagopyrum esculentum Moench) field with a low ExK content, despite the application of K, in Fukushima Prefecture, Japan (Field A), following the Tokyo Electric Power Company Fukushima Dai-ichi (No. 1) Nuclear Power Plant accident in March 2011. We examined the relationship between K concentration and clay mineral composition in the soil of Field A and compared the findings with another field in Fukushima Prefecture (Field B) to clarify whether K applied to the soil was leached or remaining fixed. Pot experiments showed that K concentration in water seepage from pots following irrigation was significantly lower in pots from Field A than in those from Field B. Soil ExK content after soybean cultivation was lower in soils of Field A than those of Field B. These results indicate that K applied to Field A was fixed in the soil. Analysis of clay mineral composition confirmed the distinctive vermiculitic nature of Field A soils. This clay mineralogy would be associated with the higher K fixation ability of Field A than Field B soils. This study demonstrated that K fixation in vermiculite was a factor preventing the increase in ExK content from K application to Field A.