Carboxylate-containing chelating agent interactions with amorphous chromium hydroxide: Adsorption and dissolution

Anthropogenic chelating agents and biological chelating agents produced by indigenous organisms may dissolve Cr^III (hydr)oxides in soils and sediments. The resulting dissolved Cr^III-chelating agent complexes are more readily transported through porous media, thereby spreading contamination. With this work, we examine chelating agent-assisted dissolution of amorphous chromium hydroxide (ACH) by the (amino)carboxylate chelating agents iminodiacetic acid (IDA), nitrilotriacetic acid (NTA), tricarballylic acid (TCA), citric acid (CIT), ethylenediaminetetraacetic acid (EDTA), trans-1,2-cyclohexanediaminetetraacetic acid (CDTA), and trimethylenediaminetetraacetic acid (TMDTA). The extent of chelating agent adsorption onto ACH increased quickly over the first few hours, and then increased more gradually until a constant extent was attained. The extent of chelating agent adsorption versus pH followed “ligand-like” behavior. All chelating agents with the exception of TCA and IDA effectively dissolved significant amounts of ACH within 10 days from pH 4.0 to 9.4. IDA dissolved ACH below pH 6.5 and above pH 7.5. Rates of ACH dissolution normalized to the extent of chelating agent adsorption were pH dependent. IDA, NTA, CIT, and CDTA exhibited an increase in normalized dissolution rate with decreasing pH. EDTA and TMDTA exhibited a maximum in normalized dissolution rate near pH 8.5. Use of acetic acid as a pH buffer in experiments decreased the extent of chelating agent adsorption for IDA, NTA, and CIT but increased normalized rates of chelating agent-assisted dissolution for all chelating agents except EDTA. The results from this study provide the necessary information to calculate the extents and time scales of ACH dissolution in the presence of (amino)carboxylate chelating agents.     

珠江三角洲不同成土母质发育水稻土镉活动性差异及其影响因素

随着我国经济社会的快速发展,土壤重金属的超标问题越来越突出,尤其是Cd。土壤Cd活动性受到各种因素的影响,但成土母质对土壤Cd活动性影响的研究成果还鲜有报道。以珠江三角洲为研究区,系统采集了由第四纪沉积物、酸性侵入岩和陆源碎屑岩3种不同成土母质发育形成的水稻土样品235件,查明了土壤理化特征,探讨了Cd全量及其活动态的影响因素。结果表明：不同成土母质发育形成的水稻土理化性质、Cd全量及其活动态的影响因素存在差异。第四纪沉积物发育形成的水稻土CaO、K₂O、Na₂O、TFe₂O₃、阳离子交换量(CEC)、pH、有机质、黏粒平均含量显著高于酸性侵入岩和陆源碎屑岩,Cd超标最为严重,不同方法提取的Cd活动态含量也最高;陆源碎屑岩发育形成的水稻土中Cd全量与土壤理化指标的相关性均强于其他两类成土母质;酸性侵入岩发育形成的水稻土中Cd全量与土壤理化指标的相关性较弱。Cd全量对其活动态含量有重要影响,此外,第四纪沉积物发育的水稻土中Cd活动态含量与pH、有机质和TFe₂O₃     

Readily dispersible clay and its role in the mobility of transition metals Cd2+, Cu2+ and Zn2+ in an alkaline alluvial soil

Readily dispersible clay is the part of the clay fraction in soils that potentially disperses in water when a small amount of mechanical energy is applied to soil. Column and batch experiments were conducted to identify the effect of readily dispersible clay on the mobility of some metal ions in a disturbed soil sample. The clay fraction (<0.002 mm) was separated from an alkaline Vertisol from the Nile River Delta. X-ray diffraction technique was used to identify minerals present in the clay fraction. Clay suspensions and deionized H₂O solutions of Cd²⁺, Cu²⁺, and Zn²⁺ were prepared and used as influents in soil columns. Adsorption capability of the studied soil among the three metal ions was investigated. The results showed high adsorption capacity of Cd²⁺, Cu²⁺, but not Zn²⁺ for the studied soil. Cu²⁺ was the highest adsorbed metal by soil and its sorption increased at small equilibrium concentrations compared with Cd²⁺ and Zn²⁺. For the three studied metal ions, Langmuir model represented the best fit to the adsorption data. The concentration of Zn²⁺ and Cd²⁺ in leachates increased as the leaching solution volume increased, while Cu²⁺ showed a homogeneous distribution throughout the soil column. According to DTPA extractable metals, Zn²⁺ was appeared at greater depths than Cd²⁺, while Cu²⁺ had homogeneous distribution through the soil column.     

The spatial distribution of potassium status and clay mineralogy in relation to different land-use types in a calcareous Mediterranean environment

In order to investigate changes caused in clay mineralogy and potassium (K) status by different land-use types, 42 soils samples (0–30 cm) were monitored and analyzed. Soil samples belonging to Reference Soil Groups of Cambisols and Vertisols were collected from three neighboring land uses involving cropland (under long-term continuous cultivation), grassland, and forestland. The soils reflected an alkaline and calcareous aspect as were characterized by high pH (mean of 7.1 to 7.5) and calcium carbonate equivalent (mean of 35 to 97 g?kg^?1) in the three land-use types. X-ray diffraction patterns of the clay fraction showed that the soils were mainly composed of illite, smectite, chlorite, and kaolinite. Chlorite and kaolinite remained unweathered irrespective of land use and soil types, soil processes, and physicochemical attributes assessed. Some changes in the XRD diffractograms of illite and smectite (the intensity or the position of peaks) were observed in the cultivated soils compared to those of the adjoining grassland that may explain the dynamics of the K trapped in illite interlayer sites. Potassium issues reflected a heterogeneous response to changes in land-use types. In light of this, a pronounced variation in soluble K (4–22 mg?kg^?1), exchangeable K (140–558 mg?kg^?1), and non-exchangeable K (135–742 mg?kg^?1) appeared among the land-use types for both Cambisols and Vertisols, corresponding to variability in clay content, nature and type of clay mineral (mainly illite and smectite), cation exchange capacity (CEC), and soil organic carbon (SOC). In general, the largest amounts of soluble K and exchangeable K were recorded in the forestland, whereas the highest contents of non-exchangeable K were found in the grassland for both Cambisols and Vertisols. Exchangeable K, available K, CEC, and clay contents in the soils with higher smectite values (25–50 %) were significantly different (P?≤?0.05) compared to those of the lower smectite values (10–25 %). This suggests that smectite is a major source for surface sorption of K in the studied soils.     

The development of a multi-surface soil speciation model for Cd (II) and Pb (II): Comparison of two approaches for metal adsorption to clay fractions

The mobility of toxic metals in soils or sediments is of great concern to scientists and environmentalists since it directly affects the bioavailability of metals and their movement to surface and ground waters. In this study, a multi-surface soil speciation model for Cd (II) and Pb (II) was developed to predict the partition of metals on various soil solid components (e.g. soil organic matter (SOM), oxide mineral, and clay mineral). In previous study, the sorption of metal cations on SOM and oxide minerals has been evaluated by thermodynamically based surface complexation model. However, metal binding to soil clay fractions was normally treated in a simplistic manner: only cation exchange reactions were considered and exchange coefficient was assumed unity. In this study, the binding of metals onto clays was described by a two-site surface sorption model (a basal surface site and an edge site). The model was checked by predicting the adsorption behavior of Cd (II) and Pb (II) onto three selected Chinese soils as a function of pH and ionic strengths. Results showed that the proposed model more accurately predicted the metal adsorption on soils under studied condition, especially in low ionic strength condition, suggesting that adsorption of metals to soil clay fractions need to be considered more carefully when modeling the partition of trace elements in soils. The developed soil speciation model will be useful when evaluating the movement and bioavailability of toxic metals in soil environment.     

水稻土中重金属元素Cd、Pb的竞争吸附 ——以长株潭地区水稻土为例

对中国南方的3个水稻土样品进行了Cd、Pb单一离子和混合离子吸附特点的研究。结果表明,3个水稻土样品中Cd、Pb的吸附特点都相似,Langmuir等温方程可很好地描述Cd、Pb的吸附等温线。3个土壤样品中,有较高pH值和较低有机物、CEC浓度、粘土含量、高岭石含量的2个土壤样品对Cd、Pb有较大的吸附量,且其等温吸附拟合的最大吸附量(B)也较大。在两组分混合溶液中,尽管共存离子的存在影响了土壤对单一离子的吸附,同时土壤对Cd的吸附在一定程度上受影响的程度大,但3个土壤样品都表现出对Pb有强的吸附能力。在3个土壤样品中,Langmuir等温方程中Pb的健合能常数(K)都大于Cd的健合能常数(K),混合溶液中的K值高于单一溶液的K值,表明2种金属离子对吸附位点的竞争提高了特定吸附位点的保持力,使金属离子在土壤中特定位点的吸附更加坚固。     

氨基膨润土对铜镍镉污染土壤的钝化修复研究

采集土壤,加入铜、镍和镉制成重金属污染土壤。以四乙烯五胺改性膨润土和膨润土原土作为修复剂,通过模拟酸雨和混合提取剂提取有效态重金属,评价膨润土和氨基膨润土对土壤中铜、镍、镉的钝化效果。结果表明:p H=3. 5的模拟酸雨对各污染土壤中重金属离子的提取率均在0. 1%以下。混合提取剂对污染土壤中有效态金属的提取能力比模拟酸雨强很多。添加膨润土原土和氨基膨润土均能钝化土壤中的铜、镍和镉,氨基膨润土上嫁接的氨基对金属有络合作用,因而比膨润土原土对铜、镍和镉具有更强的钝化能力。综合评价表明氨基膨润土是一种对铜、镍和镉污染土壤具有应用前景的钝化修复材料。     

Investigation of bacterial hopanoid inputs to soils from Western Canada

Hopanoids have been widely used as characteristic biomarkers to study inputs of bacterial biomass to sediments because they are preserved in the geologic record. A limited number of studies have been performed on hopanoid biomarkers in soils. The present study examined the distribution and potential preservation of hopanoids in soils that are developed under different climatic conditions and varying vegetative inputs. Solvent extraction and sequential chemical degradation methods were employed to extract both “free” and “bound” hopanoids, from three grassland soils, a grassland–forest transition soil, and a forest soil from Western Canada. Identification and quantification of hopanoids in the soil samples were carried out by gas chromatography–mass spectrometry. Methylbishomohopanol, bishomohopanol and bishomohopanoic acid were detected in all solvent extracts. The base hydrolysis and ruthenium tetroxide extracts contained only bishomohopanoic acid at a concentration range of 0.8–8.8 μg/gC and 2.2–28.3 μg/gC, respectively. The acid hydrolysis procedure did not release detectable amounts of hopanoids. The solvent extraction yielded the greatest amounts of “free” hopanoids in two of the grassland soils (Dark Brown and Black Chernozems) and in the forest soil (Gray Luvisol). In contrast, the chemical degradation methods resulted in higher amounts of “bound” hopanoids in the third grassland soil (Brown Chernozem) and the transition soil (Dark Gray Chernozem), indicating that more hopanoids exist in the “bound” form in these soils. Overall, the forest and the transition soils contained more hopanoids than the grassland soils. This is hypothesized to be due to the greater degradation of hopanoids in the grassland soils and or sorption to clay minerals, as compared to the forest and transition soils.     

水稻土中重金属元素Cd、Pb的竞争吸附——以长株潭地区水稻土为例

对中国南方的3个水稻土样品进行了Cd、Pb单一离子和混合离子吸附特点的研究。结果表明,3个水稻土样品中Cd、Pb的吸附特点都相似,Langmuir等温方程可很好地描述Cd、Pb的吸附等温线。3个土壤样品中,有较高pH值和较低有机物、CEC浓度、粘土含量、高岭石含量的2个土壤样品对Cd、Pb有较大的吸附量,且其等温吸附拟合的最大吸附量（B）也较大。在两组分混合溶液中,尽管共存离子的存在影响了土壤对单一离子的吸附,同时土壤对Cd的吸附在一定程度上受影响的程度大,但3个土壤样品都表现出对Pb有强的吸附能力。在3个土壤样品中,Langmuir等温方程中Pb的健合能常数（K）都大于Cd的健合能常数（K）,混合溶液中的K值高于单一溶液的K值,表明2种金属离子对吸附位点的竞争提高了特定吸附位点的保持力,使金属离子在土壤中特定位点的吸附更加坚固。     

Changes in physical and chemical properties of three soil types in India as a result of amendment with fly ash and sewage sludge

The use of coal fly ash and domestic sewage sludge in agriculture is being considered as one of the methods for recycling of these wastes in an environmental beneficial manner. Mixtures with soil were prepared at different proportions of fly ash and sludge, either alone or in combination at a maximum application rate of 52 t ha^-1. The changes in the selected properties and heavy metal contents of three soil types in India were studied after incubating the respective mixtures for 90 days at near field capacity moisture level. Sewage sludge, due to its acidic and saline nature, high organic matter and heavy metals content, had more impact on soil properties than the fly ash. Sludge application produced several changes including an increase in available nitrogen, organic carbon, salinity and water-holding capacity of the soils. The concentrations of major cations and heavy metals also increased because of the sludge application and the pH was decreased. However, the levels of individual metal concentrations in all the mixture types were below the allowable limits prescribed by several environmental agencies. Using fly ash either alone or in equal quantity with sewage sludge had little influence on soil properties and heavy metal content. The relative availability (RA) of heavy metals in three soils amended with 52 t ha^-1 of sewage sludge was observed to be highest in oxisol, followed by alfisol and vertisol.     

Comparison of extractability of Cd, Cu, Pb and Zn with sequential extraction in contaminated and non-contaminated soils

Various extraction procedures were employed for measuring extractable concentrations of potential toxic elements in soil. The extractability of Cd, Cu, Pb and Zn in four contaminated and four non-contaminated soils of Japan, was compared by single extraction (CaCl₂, DTPA, NH₄Cl, 0.1 M HCl and 1 M HCl ) and sequential extraction procedures [(six operationally defined chemical phases, viz. water soluble (Fl), exchangeable (F2), carbonate (F3), oxide (F4), organic (F5) and residual (F6) fractions)]. Extractability of metals from soils samples varied depending on metals and/or extradants used. Among the extradants, 1 M HCl extracted the largest proportion of Cd (79 to 96% of total), Cu (61 to 83%), Pb (51 to 99%) and Zn (23 to 52%) from soils followed by 0.1 M HCl, NH₄Cl, DTPA and CaCl₂. In all the extradants, the proportion of extractability of metals was higher in the contaminated soils than the non-contaminated soils. Regardless of soils and extradants, relative extractability was higher for Cd as compared to other three metals. The use of 1 M HCl may be recommended for first-level screening of soil contamination with heavy metals. The other four weak extradants are believed to provide a better assessment of bioavailable/mobile metals content in soils than 1 M HCl extradant. However, 0.1 M HCl mobilized all four metals irrespective of soil types, therefore, might be the best choice if only one extradant is to be used. The sequential extraction procedures showed 22 to 64% of total Cd was in the mobile fraction (sum of Fl to F3), while the corresponding values for Cu, Pb and Zn in this fractions were 2 to 23% suggesting higher mobility of Cd than other three metals. The single extraction procedures are simple and easy to perform and obtained results are comparable with sequential extraction procedure.     

Single element and competitive sorption of copper, zinc and lead onto a Luvisol profile

The sorption parameters of Cu, Zn and Pb are related to the composition of the different genetic horizons of a Luvisol profile in batch sorption experiments. The affinities of metals towards the soil samples from different horizons followed the same sequence, e.g. Pb≥C>>Zn. By far the highest metal retention was found in the C_k horizon due to the alkaline conditions. It is followed by the A horizon with its high organic matter content, while the lowest sorption capacity was found in the Bt horizon. In the horizons free of carbonate, primarily Pb and Cu were immobilized. The studied soil can be characterized by high amount of organic matter, clay accumulation horizon, as well as calcareous subsoil. This kind of profile development makes soils able to immobilize a significant metal pollution.     

渭南黄土沉积中十五万年来的古土壤及其形成时的古环境

关中盆地渭南地区十五万年来的黄土剖面记载了６个大的成壤期。本文对古土壤形成时的古环境进行了解译，并对它们在不同分类系统中的位置进行评价。全新世土壤Ｓ０是联合国土壤分类中的淋溶湿草原土。马兰黄土中包含两层古土壤，属典型黑钙土。Ｓ１古土壤由三层土壤复合组成，从上到下依次为典型黑钙土、淋溶湿草原土和深色淋溶土。成壤期与全球冰量较小的时期相对应，但古土壤的类型及发育程度与深海氧同位素所推测的全球冰量的变化有很大的不一致性，相反许多方面与北半球夏季太阳辐射的变化有较大的可比性。     

江西贵溪冶炼厂重金属环境污染特征及生态风险评价

金属矿物开采、冶炼等活动引起土壤金属污染是世界普遍存在的问题,由此引起的人类健康问题和环境生态的恶化,越来越受到世界各国环境学家关注。本文调查了冶炼厂周围农田重金属元素的纵向分布,并利用连续浸提法分析主要污染元素的化学形态,结果表明,土壤Cu,Zn,Cd和Pb的非残渣态含量远远高于未污染土壤,污染元素的生物可利用性高;同时采用多指标生态评价体系,对铜矿冶炼厂周围农田土壤重金属污染进行综合的潜在生态风险评价。根据风险指标体系和空间分异规律,将冶炼厂周围农田分成3种生态风险功能区。     

Effect of organic matter and selected heavy metals on sorption of acenaphthene,fluorene and fluoranthene onto various clays and clay minerals

The effects of organic matter (80% humic and 15% fulvic acid) and coexistence of heavy metals (Ni, Pb and Zn) on sorption of three polycyclic aromatic hydrocarbons (PAHs)—acenaphthene, fluorene and fluoranthene—were examined for kaolinite, 60% kaolinite?+?40% sand, and 43% kaolinite?+?42% sand?+?15% bentonite. In total 108 batch sorption tests of PAHs were conducted for three types of clay mineral mixtures in six possible combinations of soil organic matter and heavy metal contents from no heavy metals and organic matter added to maximum organic matter added with spiked heavy metals. Results showed that the existence of metals increased the sorption of PAHs onto kaolinite from 4.7% for acenaphthene to 17.9% for fluoranthene. Organic matter in a kaolinite-sand-bentonite matrix could increase PAH sorption by up to 140% for fluoranthene. In all cases, increases were greater for fluoranthene, a larger PAH molecule. Heavy metals coexisting with organic matter led to enhanced sorption of PAHs compared to clay minerals without organic matter. Synergistic effects of organic matter and heavy metals on PAH sorption increments in the mixtures studied were such that the overall sorption could be 10–41% higher than that based on summation of the separate effects of metals and organics.     

Clay mineralogy, grain size distribution and their correlations with trace metals in the salt marsh sediments of the Skallingen barrier spit, Danish Wadden Sea

To understand the behavior of trace metals in the salt marsh at Skallingen, Danish Wadden Sea, we investigated a profile from surface to 25?cm depth of the salt marsh sediment, focusing primarily on clay mineralogy and grain size distribution of the sediments and their relationship with trace metals. The clay assembly of the sediment consists of illite, kaolinite and much less chlorite and smectite. The major clay minerals of illite, kaolinite as well as chlorite correlate very poorly with all the trace metals investigated, due probably to the weak competing strength of these clays compared with the other adsorbents and to low availability of the mobile trace metals in the system. Correlation between trace metals and clay minerals may therefore be used as an indicator in environmental assessment. Fine grain fractions of the sediment increased markedly after salt marsh invasion in about 1931 but decreased after 1964. This increase was contributed mainly by the grains finer than 20???m while the fraction of 40?C63???m actually decreased soon after the invasion. The relation between most of the trace metals and grain size distributions is close in general but far from linear. The drastic turning point is observed at about 30???m, around where the correlation coefficient r drops from 0.8 to 0.1. Adsorption is the controlling mechanism for the behavior of trace metals in the salt marsh. Fe/Mn (hydr)oxides and organic matter play the key role.     

Adsorption of copper and zinc onto natural clay in single and binary systems

Calcareous and smectitic clay samples from the Coniacian–Lower Campanian system, Tunisia, were used as adsorbents for the removal of copper and zinc from aqueous solutions in single and binary systems. Calcareous clay sample was treated with acetic acid to obtain carbonate-free sample that was also used for metals removal. The adsorption of metal ions onto natural clay was tested in a batch method by mixing 1 g/L of each sample with a metal ion solution of zinc (300 μmol/L) and/or copper 600 μmol/L under the operating pH of 6, and agitation speed of 200 rpm within the equilibrium time of 60 min at 25 °C for single and binary systems. Our results showed that natural clay samples were mainly composed of silica, alumina, iron, and magnesium oxides. Adsorption data showed that the studied clay samples removed substantial amounts of heavy metals in single and mixed systems. Initial solution pH and carbonates contents enhanced the removal capacities of the studied clay samples, confirming their strong influencing effects. Thermodynamic parameters indicated an endothermic adsorption for metals removal by calcareous clay, but exothermic process for the smectitic sample. These results suggest that the Late Cretaceous clays, Tunisia, can be effectively used as natural adsorbents for the removal of toxic heavy metals in aqueous systems.     

Amelioration of soil acidity,Olsen-P,and phosphatase activity by manure- and peat-derived biochars in different acidic soils

To increase soil productivity, ameliorate nutrient scarcity, and reduce metal toxicity in highly weathered acidic soils usually requires fertilizer and lime application. Effects of three biochars on soil acidity, Olsen-phosphorus (P), phosphatase activities, and heavy metal availability were investigated to test potential of these biochars as soil amendments in highly weathered acidic soils. Incubation experiments were conducted for 6 weeks with three acidic soils: Alfisol, Ultisol, and Oxisol. Three biochars were derived from chicken manure (CMB), pig manure (PMB), and peat moss (PB) at 400 °C and applied at 1 or 2% (wt/wt). The addition of the three biochars increased Olsen-P in the three acidic soils in the following order: CMB?>?PMB?>?PB. Application of 2% CMB increased Olsen-P contents by 2.41-, 7.4-, and 1.78-fold in the Ultisol, Oxisol, and Alfisol compared with controls, respectively. Moreover, CMB increased the soil pH, electrical conductivity (EC), cation exchange capacity (CEC), and alkaline phosphatase activity, but reduced exchangeable acidity, acid phosphatase activity, and the availability of heavy metals—more effectively than PMB and PB. Addition of CMB increased soil pH by 0.90, 0.90, and 0.92 units for the Alfisol, Ultisol, and Oxisol, respectively, correspondingly followed by 0.80, 0.84, and 0.87 units for PMB and 0.15, 0.28, and 0.25 for PM. Changes in EC, CEC, and exchangeable acidity followed the same order for the three soils: CMB?>?PMB?>?PB. The results suggested that the magnitude of changes in soil properties and Olsen-P contents depended on biochar type and application rate. Application of CMB increased nutrient availability and reduced the availability of heavy metals more than other amendments. Due to higher pH, EC, and CEC, and greater concentrations of carbon, nitrogen, and exchangeable calcium and potassium, incorporation of CMB should be a better cost-effective method to correct soil acidity and improve fertility and Olsen-P contents in Ultisols and Oxisols from tropical and subtropical regions of the world.     

Residual strength of slip zones of large landslides in the Three Gorges area, China

Slip zones of the large landslides in the Three Gorges area are commonly composed of fine-grained soils with substantial amount of coarse-grained particles, particularly gravel-sized particles. In this study, residual strength of the soils from slip zones of these landslides were examined in relation to their index properties based on a survey of 170 landslides. It was found that laboratory-determined residual friction angle using gravel-free fraction of the disturbed soils from the slip zones was closely related to clay content, liquid limit and plasticity index. On the other hand, in-situ residual friction angle of these soils (i.e. including gravel fraction) showed very weak correlations with clay content and Atterberg limits, but was largely dependent on gravel and fines (clays + silts) contents, increasing with gravels and decreasing with fines, and displayed strong linear correlation with the ratio of gravel to fines contents. These observations indicate that among the index properties, clay content and Atterberg limits can be used to estimate residual strength of the soils finer than 2 mm, but they are not appropriate evaluate the residual strength of the soils containing considerable amount of gravel-sized particles. For the latter, particle size distribution (particularly the ratio of gravel to fines contents) appears to be a useful index. Additionally, it was found that there was no identifiable correlation between relative abundance of individual major clay minerals and residual friction angles of both gravel-free fraction of disturbed and in-situ soils, suggesting that influence of clay minerals on residual strength of these soils can not be simply evaluated based on their abundance.     

全新世与上次间冰期气候差异的古土壤记录

目前国际上对全新世与上次间冰期的气候差异还存在着较大的争议。对西欧阿晴里姆黄土中全新世和上次间冰期古土壤（埃姆古土壤）,中国黄土中S₀及S₁的对比研究表明,埃姆古土壤和S₁是典型的复合土壤,记载了相同的沉积-成壤事件序列,并与深海氧同位素记录有很好的一致性。第一成壤期与氧同位素阶段5e相对应,代表了典型的间冰期气候。西欧在该时期形成的土壤与全新世土壤的成壤过程基本相同,二者反映了类似的气候条件;而中国黄土中S₀和S₁则具很大差异,这表明我国北方最后两次间冰期的气候条件显著不同。青藏高原在中更新世末期以来的隆升对季风环流的影响是值得注意的原因之一。