砂姜黑土的粘粒矿物组成和蒙皂石来源的探讨

对不同地区的几个砂姜黑土剖面的粘粒矿物进行了 X 射线衍射分析,结果表明均以蒙皂石为主,其次为伊利石,高岭石和蛭石含量较少,仅山东高密的砂姜黑土削面含少量绿泥石。这与毗邻土壤类型迥然不同。对黑土层石英砂的 SEM 观察表明,砂姜黑土的母质均为洪(冲)积-湖沼沉积型。笔者认为,砂姜黑土中高含量的蒙皂石主要系流水悬浮而来,在湖泊静水环境中沉淀富集而成,其来源范围比粗骨颗粒部分更广泛。     

Zinc sorption–desorption by sand,silt and clay fractions in calcareous soils of Iran

Zinc sorption–desorption by sand, silt and clay fractions of six representative calcareous soils of Iran were measured. Sand, silt and clay particles were fractionated after dispersion of soils with an ultrasonic probe. Zinc sorption analysis was performed by adding eight rates of Zn from 6 to 120 μmol g^?1. For the desorption experiment, samples retained after the measurement of Zn sorption were resuspended sequentially in 0.01 M NaNO₃ solution and shaken for 24 h. Results indicated that Zn sorption by soil fractions increased in the order clay > silt > sand, and correlated negatively with CaCO₃ content and positively with cation exchange capacity (CEC) and smectite content. Results indicated that for all fractions, the Langmuir equation described the sorption rates fairly well. In contrast to sorption, Zn desorption from soil fractions increased in the order sand > silt > clay, and correlated positively with CaCO₃ content, CEC and smectite content. Results showed that parabolic diffusion and two constant equations adequately described the reaction rates of Zn desorption. In general, for all soils studied, the coarser the particle size, the less Zn sorption and more Zn desorption, and this reflects much higher risk of Zn leaching into groundwater or plant uptake in contaminated soils.     

Potassium fixation of some calcareous soils after short term extraction with different solutions

This investigation was done to determine the release of potassium (K) from five calcareous soils of southern Iran using 0.025 M CaCl₂, HCl and citric acid during six successive extractions and to study the K fixation capacity of the soils after K release experiment. Mineralogical study indicated that Vertisols and Mollisols were dominated with smectites; while other soils had illite, chlorite, palygorskite and smectite. Results indicated that citric acid extracted more K than CaCl₂ and HCl (137 vs. 111 and 113 mg kg^?1, respectively). The analysis of calcium (Ca), magnesium (Mg) and K concentrations in the solutions suggests that the exchange of K with soluble Ca and Mg (originated from dissolution of carbonates by acidic solutions) is the main mechanism of K release, but citrate is able to dissolve K-bearing minerals and release K in slightly calcareous soils. Soils with more illite released more K. Potassium fixation capacity of soils increased after extractions of soils with different extractants from 324 to 471 mg kg^?1, with no significant difference. It is suggested to apply more K fertilizers in K-depleted calcareous soils and use of different solutions for extracting K from soil minerals may be a temporary and short term solution.     

Clay Addition to Sandy Soil——Influence of Clay Type and Size on Nutrient Availability in Sandy Soils Amended with Residues Differing in C/N ratio

Addition of clay-rich subsoil to sandy soil results in heterogeneous soil with clay peds(2-mm) or finely ground( 2 mm) clay soil(FG), which may affect the nutrient availability. The aim of this study was to assess the effect of clay soil particle size(FG or peds)and properties on nutrient availability and organic C binding in sandy soil after addition of residues with low(young kikuyu grass,KG) or high(faba bean, FB) C/N ratio. Two clay soils with high and low smectite percentage, clay and exchangeable Fe and Al were added to a sandy soil at a rate of 20%(weight/weight) either as FG or peds. Over 45 d, available N and P as well as microbial biomass N and P concentrations and cumulative respiration were greater in soils with residues of KG than FB. For soils with KG residues,clay addition increased available N and initial microbial biomass C and N concentrations, but decreased cumulative respiration and P availability compared to sandy soil without clay. Differences in measured parameters between clay type and size were inconsistent and varied with time except the increase in total organic C in the 53 μm fraction during the experiment, which was greater for soils with FG than with peds. We concluded that the high exchangeable Fe and Al concentrations in the low-smectite clay soil can compensate a lower clay concentration and proportion of smectite with respect to binding of organic matter and nutrients.     

松嫩平原北部寒变性土的研究

2008年在黑龙江省松嫩平原北部的北安市(47.53°N,126.16°E)和依安县(47.45°N,125.13°E)所在的乌裕尔河阶地上的寒均腐土地区,进一步观察了7个土壤剖面,发现其中有3个剖面具有变性特征。其母质有第四系中更新世(Qp2)黄土性冲-湖积物,和白垩系的泥页岩风化物(K2)。诊断特征:全剖面黏粒(<2μm)含量330～480 g.kg-1;心土层棱柱状结构破碎成棱块状;可见楔形结构,或滑擦面;旱季土壤开裂,冻融期和雨季闭合。线膨胀系数可高达0.19 cm.cm-1,土壤代换量在34～37 cmol.kg-1之间。黏土矿物以伊蒙混层、蒙皂石为主,控制层段的蒙皂石总量约占66%～70%。按美国土壤系统分类检索,符合变性土纲的鉴定标准,将其划归寒变性土亚纲(Cryerts),其中土类有简育寒变性土(Haplocryerts),亚类有典型简育寒变性土(Typic Haplocryerts)和艳色简育寒变性土(Chromic Haplocryerts)。研究认为,本地的寒变性土主要是由于原母质和某些寒均腐土的心土层累积了大量膨胀性的伊蒙混层和蒙皂石黏土矿物,在干湿交替的气候和加速土壤侵蚀等综合因素影...     

Adsorption isotherms of copper and zinc in clay minerals of calcareous soils and their effects on X-ray diffraction

Reactions of elements with the water mineral interface are important and affect their bioavailability and transportation within soil. Effects of metal sorption on X-ray-diffraction (XRD-photographs) of clay minerals have been not studied. Therefore, sorption experiments were done on clay fractions of two calcareous soils using 12 concentrations of 0–2000 mg L^?1 Zn(NO₃)₂ and Cu(NO₃)₂. Langmuir and Freundlich isotherms’ coefficients were determined. After sorption, XRD-diffraction were prepared and compared with those of initial samples. Langmuir (R² = 0.996–0.999 and SE = 0.001–0.002) and Freundlich equation were the best-model for Zn and Cu-sorption, respectively. Sorption energy was higher for Zn than Cu, whereas the maximum concentration of sorbed-Cu was higher than that of Zn. Distribution coefficient (K_d) of Cu were more (threefold) than that of Zn. The K_d values representing the slope of Freundlich isotherms decreased according to linear regression equations (R² = 0.72–0.91) as the equilibrium concentrations of metals increased. No significant differences were observed among XRD-photographs of applied concentrations (some negligible differences were found in position/sharpness of peaks). Dry-XRD-method resulted in omission of intensity peaks at 2θ which may interfere in recognition of clays that show a maximum intensity >1.4 nm in the mentioned 2θ. Zinc can become more leachable especially in Shekarbani-soil-series, whereas, Cu highly adsorb on clay minerals and can show less tendency to transportation.     

Phosphate sorption to matrix and fracture wall materials in a Glossaqualf

Phosphate retaining properties of macropore wall materials may influence the extent of phosphate leaching via preferential flow. Phosphate sorption to soil matrix material has been compared with sorption to fracture wall materials consisting of inner iron-oxide depleted albic coatings rimmed by reddish iron-oxide enriched quasicoatings. The latter contains 15 times as much Fe oxide, 2 times as much Al (hydr)oxide and 5–6 times as much total P than the albic material, which represent the most P-depleted material in the profile. Oxalate extractable P (P_o) amounts to of the total P contents of the samples. Smectite predominates in the fracture walls and acid subsoils, but has partly transformed into hydroxy-interlayered smectite (HIS) in the upper limed soil horizons. Langmuir parameters derived from phosphate sorption isotherms show no correlation for sorption to whole soil samples and the corresponding clay fractions. The phosphate sorption capacity at a threshold equilibrium concentration of 10 μM (P_ads^t (10 μM)) is measured as the content of P_o plus the amount of phosphate sorbed during 7 days, and can be related to Al_o+Fe_o: P_ads^t (10 μM)=(0.0404±0.0046)·(Al_o+Fe_o)***+3.569. The P_ads^t (10 μM) values vary between 4 and 14 mmol P kg⁻¹, lowest in the albic fracture walls and highest in the iron enriched quasi-coatings. The sorption capacity of the metal oxide free clay does not appear to correlate with smectite or HIS contents. In total, the clay fraction contributes with about 50% of the whole soil sorption capacity in agreement with 40–60% of the total soil Al_o+Fe_o being present in the clay fraction. At a solution phosphate concentration of 10 μM, the Ap horizon is found to be almost phosphate saturated whereas subsoil horizons including the fractures have phosphate saturations ≤50% and, hence, can strongly sorb P. The low phosphate saturation of fracture walls indicates that they do not act as major sinks of phosphate-rich solutions from topsoil horizons, either due to kinetic constraints, or due to a flow pattern not allowing P-rich solution to percolate fractures.     

Short‐time clay‐mineral evolution in a soil chronosequence in Oléron Island (France)

Major weathering sequences in soils are well established; however, knowledge on rates of mineral transformations remains unknown, because it is often difficult to date precisely soil processes. This work was carried out on soils developed on recent (< 188 y) sand dunes on the W coast of Oléron Island (France). The coast has been protected against marine and wind erosion by constructing five consecutives barriers close to the coastline since 1820 (1820, 1864, 1876, 1889, 1948) defining the maximum age of the soil parent material, as before the areas between the barriers were under water. Soils on the older dunes have low clay content (> 94% of sand) and exhibit a bleached E horizon that overlies a yellowish brown B horizon. The process responsible for their formation is podzolization promoted by the high permeability of the material and complexing organic matter produced by coniferous vegetation. Initial mineralogy of C horizons is homogenous and constituted of chlorite, illite, illite/smectite mixed‐layer minerals, and kaolinite, quartz, calcite (≈ 8% related to shell fragments), and feldspars. The initial clay‐mineral assemblage of the E horizons is dominated by illite (well‐crystallized WCI and poorly crystallized PCI) and chlorite. With progressive podzolization, poorly crystallized illite is first transformed to illite/smectite mixed‐layer minerals and in a further step into smectite. In addition, transformation of well‐crystallized illite leads to formation of ordered illite/smectite mixed‐layer minerals in the E horizons, which is not commonly described in soils. In the B horizons, illite/smectite mixed‐layer minerals are present with traces of smectite, as well as Al and Fe oxi‐hydroxides as revealed by DCB and oxalate chemical extractions. This chronosequence illustrates that over short distances and short time (< 188 y) intense mineral weathering and soil development occur. Major clay‐mineral changes occur between 132 and 188 y in agreement with development of the pine forest producing acidic litter.     

水溶性有机碳在各种粘土底土中的吸附：土壤性质的影响

Clay-rich subsoils are added to sandy soils to improve crop yield and increase organic carbon (C) sequestration; however, little is known about the influence of clay subsoil properties on organic C sorption and desorption. Batch sorption experiments were conducted with nine clay subsoils with a range of properties. The clay subsoils were shaken for 16 h at 4 ^oC with water-extractable organic C (WEOC, 1 224 g C L^-1) from mature wheat residue at a soil to extract ratio of 1:10. After removal of the supernatant, the residual pellet was shaken with deionised water to determine organic C desorption. The WEOC sorption was positively correlated with smectite and illite contents, cation exchange capacity (CEC) and total organic C, but negatively correlated with kaolinite content. Desorption of WEOC expressed as a percentage of WEOC sorbed was negatively correlated with smectite and illite contents, CEC, total and exchangeable calcium (Ca) concentrations and clay content, but positively correlated with kaolinite content. The relative importance of these properties varied among soil types. The soils with a high WEOC sorption capacity had medium CEC and their dominant clay minerals were smectite and illite. In contrast, kaolinite was the dominant clay mineral in the soils with a low WEOC sorption capacity and low-to-medium CEC. However, most soils had properties which could increase WEOC sorption as well as those that could decrease WEOC sorption. The relative importance of properties increasing or decreasing WEOC sorption varied with soils. The soils with high desorption had a low total Ca concentration, low-to-medium CEC and low clay content, whereas the soils with low desorption were characterised by medium-to-high CEC and smectite and illite were the dominant clay minerals. We conclude that WEOC sorption and desorption depend not on a single property but rather a combination of several properties of the subsoils in this study.