风沙土不同有机组分对氨氮的吸附特征影响

采用平衡吸附法研究了风沙土不同有机组分对氨氮的吸附特征影响。结果表明,去除腐殖质后的风沙土对氨氮的吸附能力大大降低,其碳标化饱和吸附量Гmoc和吸附分配系数Koc分别只能达到原样的68.58%和28.24%,说明腐殖质是影响氨氮在风沙土上吸附特征的主要因素;轻组有机质是一类橡胶态胶体,氨氮在橡胶态胶体上的吸附以分配作用为主,其碳标化吸附分配系数为81.58;重组有机质对氨氮的吸附起主导作用,其碳标化饱和吸附量为3350.55mg.kg-1;重组有机质是一类玻璃态胶体,氨氮在玻璃态胶体上的吸附除分配作用外,还存在孔隙填充方式的吸附;重组有机组分中的紧结态腐殖质（胡敏素）对氨氮的吸附起关键作用,其碳标化饱和吸附量可达6626.30mg.kg-1,影响机制主要为稳、紧结态腐殖质是形成土壤疏松多孔团聚体结构的重要胶结物质。在其所形成的有机-无机复合体中存在着孔隙填充方式的氨氮吸附。考查土壤对氨氮的吸附能力不但要考虑有机质的含量,更要考虑有机质的存在形态,它也是影响土壤对氨氮吸附特征的重要因素。以重组为基准,轻组有机质、稳结态腐殖质和紧结态腐殖质携载吸附态氨氮可分别按重组的0.59、1.05倍和2.50倍估算。     

风沙土不同有机组分对磷的吸附特征影响

采用平衡吸附法研究了风沙土不同有机组分对磷的吸附特征影响,可为有机组分吸附态磷携载量估算提供依据。结果表明：去除有机质后的风沙土对磷的吸附能力大大降低,其碳标化饱和吸附量（Гmo）c和吸附分配系数（ko）c分别只能达到重组的27.76%和8.45%,说明有机质是影响磷在风沙土上吸附特征的重要因素;磷在轻组有机组分上的吸附以分配作用为主（koc=51.02）;风沙土有机组分中的重组有机质对磷的吸附起主导作用（Гmoc=388.35mg.kg-1）,重组有机组分中的紧结态腐殖质（胡敏素）对磷的吸附起关键作用（Гmoc=1007.96mg.kg-1）,影响机制主要为稳、紧结态腐殖质是形成土壤疏松多孔团聚体结构的重要胶结物质。在其所形成的有机矿质复合体中除分配作用吸附外,还存在着孔隙填充方式的磷吸附;考查土壤对磷的吸附能力不但要考虑有机质的含量,更要考虑有机质的存在形态,它也是影响土壤对磷吸附特征的重要因素。以重组为基准,轻组有机组分以及重组有机组分中稳结态腐殖质和紧结态腐殖质携载的吸附态磷分别可按0.69倍以及1.37、2.75倍估算。     

菲在土壤/沉积物上的吸附-解吸过程及滞后现象的研究

实验研究了菲在土壤 /沉积物上的吸附 解吸过程。CHL土壤和HFH沉积物中有机质的固相13 CCPMASNMR谱图很相似 ,表明样品中有机质的组成差异不大 ;菲在土壤 /沉积物上的吸附过程表现出明显的非线性 ;线性模型不适合拟合菲的吸附等温线 ,Freundlich模型和双区位反应模型 (DRDM)较好地拟合了菲的吸附等温线 ,其中DRDM模型还清楚地反映菲在低浓度和高浓度下不同的吸附方式 ;另外 ,研究表明菲在土壤 /沉积物上的解吸过程中存在明显的滞后现象 ,这可能和土壤 /沉积物有机质的异质性和土壤胶团微小孔隙的存在有关。     

The effect of soil type on phosphorus sorption capacity and desorption dynamics in Irish grassland soils

Abstract. The phosphorus (P) sorption and desorption dynamics of eleven major agricultural grassland soil types in Ireland were examined using laboratory techniques, so that soils vulnerable to P loss might be identified. Desorption of P from soil using the iron-oxide paper strip test (Pfeo), water extractable P (Pw) and calcium chloride extractable P (Pcacl₂) depended on soil P status in all soils. However, soil types with high organic matter levels (OM), namely peat soils (%OM >30), had lower Pfeo and Pw but higher Pcacl₂ values compared to mineral soils at similar soil test P levels. Phosphorus sorption capacity remaining (PSCr) was measured using a single addition of P to soils and used to calculate total P sorption capacities (PSCt) and degree of P saturation (DPS). Phosphorus sorption capacities correlated negatively with % OM in soils indicating that OM may inhibit P sorption from solution to soil. High organic matter soils exhibited low P sorption capacities and poor P reserves (total P, oxalate extractable P) compared to mineral soils. Low P sorption capacities (PSCt) in peat soils were attributed to OM, which blocked or eliminated sorption sites with organic acids, therefore, P remained in the soil solution phase (Pcacl₂). In this work, peat and high organic matter soils exhibited P sorption and desorption characteristics which suggest that these soils may not be suitable for heavy applications of manure or fertilizer P owing to their low capacities for P sorption and storage.     

稻草不同途径还田对土壤结构及有机质特征的影响

通过3年的田间定位试验,系统的研究了稻草不同途径还田对稻田土壤容重、孔隙度、团聚体、有机碳总量、腐殖质组成及腐殖质结合形态的影响。结果表明,与无肥(CK)及纯施化肥(NPK)对照相比,稻草直接深埋还田(NPK+S)及利用后的菌渣、牛粪、沼渣深埋还田(NPK+FD、NPK+CD、NPK+BD)均能一定程度的降低土壤容重、增加孔隙度、增加>0.25 mm水稳性团聚体的数量和提高土壤团聚体的稳定性,有利于形成和保持良好的土壤结构;同时能提高土壤腐殖质中胡敏酸含量和HA/FA比值,增加松结态腐殖质含量和提高松/紧腐殖质比值,能一定程度的改善土壤腐殖质的组成、性质及结合形态,提高腐殖质品质,不过这4个处理间的差异不明显。稻草焚烧还田(NPK+S′)在以上方面效果均不显著,且带来严重的大气污染,并不可取。     

Microbial transformation of nitrogen compounds in soils of the southern taiga

The intensity of the processes of nitrogen mineralization, fixation, and denitrification was assessed in the high-moor peat gley, white-podzolic, pale-podzolic, burozem, low-moor peat, and soddy-gley soils of the Central Forest Biosphere Reserve (CFBR). The actual and potential activities of the nitrogen fixation and denitrification were determined using the gas-chromatographic method, and the intensity of the ammonification was determined using ion-selective electrodes. The maximum intensity of the nitrogen fixation was observed in the low-moor peat and soddy-gley soils, which are characterized by a high content of organic matter. High denitrification activity was found in the low-moor peat soil (0.31 nmol N₂O/g per h); this was determined by the excessive moistening of this soil. The processes of organic nitrogen mineralization were the most intensive in the upper (L and F) subhorizons of the litter.     

Sorption and desorption characteristics of sulfamethazine in three different soils before and after removal of organic matter

Organic matter (OM) is the most critical factor in controlling the sorption-desorption of SMZ in soil, however, few studies have explored the effects of OM removal on these important behaviors among different soils. Batch experiments were conducted to investigate the sorption and desorption characteristics of SMZ in three different soils: fluvo-aquic soil (FS), paddy soil (PS), and red soil (RS). The SMZ sorption in the evaluated soils was dominated by physisorption. The SMZ sorption capacities of FS and PS, which had a relatively higher OM content than RS, were higher than that of RS. The SMZ sorption in FS was dominated by linear partitioning. In contrast, the SMZ sorption in PS and RS was mainly nonlinear surface adsorption. After OM removal, the SMZ sorption capacity was significantly reduced in FS but increased in PS and RS. Furthermore, OM removal restrained the sorption intensity of SMZ in soils. Relatively higher OM and clay contents inhibited the SMZ desorption in FS and PS. The strong negative desorption hysteresis of SMZ in the three soils indicated that SMZ was able to move into the soil solution, thereby posing a risk to humans. Taken together, the findings of this study showed that OM indeed plays an important role during SMZ sorption-desorption in soil.     

Adsorption and Desorption of Copper in Pasture Soils

Abstract

Copper (Cu) is bound strongly to organic matter, oxides of iron (Fe) and manganese (Mn), and clay minerals in soils. To investigate the relative contribution of different soil components in the sorption of Cu, sorption was measured after the removal of various other soil components; organic matter and aluminum (Al) and Fe oxides are important in Cu adsorption. Both adsorption and desorption of Cu at various pH values were also measured by using diverse pasture soils. The differences in the sorption of Cu between the soils are attributed to the differences in the chemical characteristics of the soils. Copper sorption, as measured by the Freundlich equation sorption constants [potassium (K) and nitrogen (N)], was strongly correlated with soil properties, such as silt content, organic carbon, and soil pH. The relative importance of organic matter and oxides on Cu adsorption decreased and increased, respectively, with increasing solution Cu concentrations. In all soils, Cu sorption increased with increasing pH, but the solution Cu concentration decreased with increasing soil pH. The cumulative amounts of native and added soil Cu desorbed from two contrasting soils (Manawatu and Ngamoka) during desorption periods showed that the differences in the desorbability of Cu were a result of differences in the physico‐chemical properties of the soil matrix. This finding suggests that soil organic matter complexes of Cu added through fertilizer, resulted in decreased desorption. The proportions of added Cu desorbed during 10 desorption periods were low, ranging from 2.5% in the 24‐h to 6% in the 2‐h desorption periods. The desorption of Cu decreased with increasing soil pH. The irreversible retention of Cu might be the result of complex formation with Cu at high pH.     

源于松针的可溶性有机物对土壤多环芳烃吸附和解吸行为的影响研究

Study of the relationship between plant litter-derived dissolved organic matter（DOM） and organic pollutant transport in soil is important for understanding the role of forest litter carbon cycling in influencing pollutant behaviour and fate in forest soil.With the aim of providing insight into the capacity of plant litter-derived DOM to influence sorption and desorption of selected polycyclic aromatic hydrocarbons（PAHs） on soil, batch experiments were carried out with application of a sorption-desorption model incorporating DOM effects. Freshly fallen pine（Pinus elliottii） needles were used as the source of organic matter. Input of the pine needle litter-derived DOM was found to significantly decrease desorption hysteresis as well as soil adsorption capacity of phenanthrene（PHE） and fluoranthene（FLA）. Addition of 1 728 mg L-1dissolved organic carbon（DOC） lowered the organic carbon-normalized sorption distribution coefficient of PHE from 7 776 to 2 541 L kg-1C and of FLA from 11 503 to 4 368 L kg-1C. Decreases of the apparent sorption-desorption distribution coefficients of PHE and FLA with increased DOC concentration indicated that DOM favored desorption of PAHs from soil. Increases in the fraction of apparently dissolved PAHs were attributable to the dissolved PAH-DOM complexes, accounting for the dissolved proportions of 39% to 69% for PHE and 26% to 72% for FLA in the sorption and desorption processes as the concentration of the added DOM solution rose from 0 to 1 728 mg L-1. Our results suggest that pine needle litterderived DOM can have a substantial effect of inhibiting PAHs sorption and promoting PAHs desorption, thus leading to enhanced leaching in soil, which should be taken into account in risk assessment of PAHs accumulated in forest soil.     

Sorption and mobility of 14C-labeled imazaquin and metolachlor in four soils as influenced by soil properties

Aqueous batch-type sorption-desorption studies and soil column leaching studies were conducted to determine the influence of soil properties, soil and suspension pH, and ionic concentration on the retention, release, and mobility of [14C]imazaquin in Cape Fear sandy clay loam, Norfolk loamy sand, Rion sandy loam, and Webster clay loam. Sorption of [14C]metolachlor was also included as a reference standard. L-type sorption isotherms, which were well described by the Freundlich equation, were observed for both compounds on all soils. Metolachlor was sorbed to soils in amounts 2-8 times that of imazaquin, and retention of both herbicides was related to soil organic matter (OM) and humic matter (HM) contents and to herbicide concentration. Metolachlor retention was also related to soil clay content. Imazaquin sorption to one soil (Cape Fear) increased as concentration increased and as suspension pH decreased, with maximum sorption occurring in the vicinity of pK(a1) = (1.8). At pH levels below pK(a1) imazaquin sorption decreased as hydronium ions (H3O+) increased and competed for sites. NaCl was more effective than water in desorption of imazaquin at pH levels near the pK(a1). Mechanisms of bonding are postulated and discussed. The mobility of imazaquin through soil columns was in the order Rion > or = Norfolk > Cape Fear > or = Webster, whereas for metolachlor it was Rion > or = Norfolk > Webster > or = Cape Fear. Imazaquin was from 2 to 10 times as mobile as metolachlor.     

Charge characteristics of soil organo-mineral complexes and their effect on phosphate fixation

Soil is a complex system of mineral and organic components. The main reactive constituent of the mineral portion of soil is clay and of organic portion is humus from the microbial transformation of organic materials in the soil. Most of the biological and physico-chemical properties and the reactions of soil are due to clay and humus, the colloidal fraction of which being the most important. Many soil phenomena of great practical and fundamental importance such as sorption and exchange of ions, interaction with organic materials etc. originate from the surface charge of clay. The presence of organic matter in the soil and its union with the mineral portion affects these charge characteristics thus affecting many important physicochemical reactions in the soil.     

Solubility,sorption and desorption of native and added cadmium in relation to properties of soils in New Zealand

Solution cadmium (Cd) concentrations and sorption and desorption of native and added Cd were studied in a range of New Zealand soils. The concentration of Cd in solution and the concentrations and patterns of native soil Cd desorbed and added Cd sorbed and desorbed varied greatly between the 29 soils studied. Correlation analysis revealed that pH was the most dominant soil variable affecting solution Cd concentration and sorption and desorption of native and added Cd in these soils. However, organic matter, cation exchange capacity (CEC) and total soil Cd were also found to be important. Multiple regression analysis showed that the log concentration of Cd in solution was strongly related to soil pH, organic matter and total Cd, which in combination explained 76% of the variation between soils. When data from the present study were combined into a single multiple regression with soil data from a previously published study, the equation generated could explain 81% of the variation in log Cd solution concentration. This reinforces the importance of pH, organic matter and total Cd in controlling solution Cd concentrations. Simple linear regression analysis could at best explain 53% of the total variation in Cd sorption or desorption for the soils studied. Multiple regression analysis showed that native Cd desorption was related to pH, organic matter and total Cd, which in combination explained 85% of the variation between soils. For sorption of Cd (from 2 μg Cd g^–1 soil added), pH and organic matter in combination explained 75% of the variation between soils. However, for added Cd desorption (%), pH and CEC explained 77%. It is clear that the combined effects of a range of soil properties control the concentration of Cd in solution, and of sorption and desorption of Cd in soils. The fraction of potentially desorbable added Cd in soils could also be predicted from a soil’s K_d value. This could have value for assessing both the mobility of Cd in soil and its likely availability to plants.     

The response of soil organic matter to manure amendments in a long-term experiment at Ultuna, Sweden

In a long-term field experiment started in 1956 on a clay loam soil at Uppsala, Sweden, changes of organic carbon in the topsoils receiving various organic amendments at the rate of 200 kg C ha^'1 year^'1 were studied to determine soil organic matter characteristics, variations of δ¹³C in the soil and to estimate a carbon balance. Fallow and mineral fertilizer without N led to a significant decrease of soil organic matter (SOM) in the soil, green manure maintained the SOM content, and animal manure and peat increased the SOM content significantly. The stable portion of the added organic materials after 37 years of continuous input was 12·8, 27·3, and 56·7%, for green manure, animal manure and peat, respectively. This was reflected by half-lives of organic carbon originating from the amendments between 3·0 (green manure) and 14·6 years (peat). The isotopic composition of SOM changed both due to mineralization (continuous fallow) and the addition of amendments is topically different from soil humus (green manure, animal manure). The isotopic effect was used to calculate the percentage of carbon derived from animal manure present for the year 1993. This value (55·4%) was larger than that derived from the carbon balance, which indicated a priming effect of the animal manure on the initial soil humus. Mineralization of microbially available organic substances led to an increase in the degree of humification on plots not receiving organic amendments. Adding peat and animal manure resulted in a decrease of the humification index due to the continuous input of poorly humified material. The extinction ratio (E₄/E₆) and ratio of fulvic acid to humic acid changed considerably in the peat treated plots. Fourier transform infrared (FTIR)-measurements of the extracts showed that peat characteristics can be detected in peat treated soils. The other amendments did not alter the characteristics of the extractable humic substances.     

Influence of organic matter on the sorption of aromatic hydrocarbons by peat and chernozem

The interaction of water-soluble monoaromatic hydrocarbons with an organic matrix of chernozem and peat was studied. As a result of high levels of soil pollution by monoaromatic hydrocarbons, soil organic matter with the high sorption capacity actively adsorbs aromatic hydrocarbons. The hydrophobic properties of aromatic compounds determine the strength of the interactions between themselves and the soil organic matrix. The presence of lipids in the organic matter of chernozem decreases the sorption of aromatic hydrocarbons because of the blocking of hydrophobic centers of the soil humic substances.     

Pyrogenic transformation of organic matter in soils of forest bogs

Natural fires on forest bogs significantly affect all the groups and fractions of peat organic matter. The type and intensity of the fires are responsible for the depth of the pyrogenic transformation of peat. In the course of thermal destruction of peat organic matter, humus substances (humic acids in particular) are accumulated, which leads to changes in the type of humus; the humus reserves may increase by 1.5–8 times. Several ways of the formation of humus components related to the intensity of a fire are suggested. The regressive evolution of bog ecosystems caused by fires is a reversible process. The humus status of pyrogenically transformed horizons and their morphology are preserved within the peat deposit as a relic characteristic of the discrete metamorphosis of the soils.     

Agronomic Evaluation of Liquid Humus Derived From Earthworm Humic Substances

Carbon (C), commonly expressed as organic matter (OM), is of vital importance in soil productivity. Liquid humus is an alkaline suspension containing humic and fulvic acids, which can facilitate C addition to the soil through the irrigation system to increase OM and soil fertility levels. Two liquid humus products were formulated from earthworm humic substances and the effects of these and other commercial products derived from leonardite, on soil and ryegrass were evaluated in a pot experiment under greenhouse conditions. On average, C application, regardless of source, increased the aerial and root dry matter, plant greenness, nitrogen (N), phosphorus (P), and potassium (K) uptake, and nutrient use efficiency. Carbon effects on plant production were larger when added over fertilized plants. Residual soil N was lowered by the application of liquid humus. No significant effect of C rate was observed on soil pH or electrical conductivity (EC) at the end of the experiment. Optimal C rates found in this study were higher than the recommended commercial ones. No major differences among earthworm liquid humus and leonardite-based products were observed; therefore the former would constitute a more sustainable alternative for organic matter additions as they are made from a renewable resource.     

Organic phosphate sorption by neutral and basic soils

Abstract

The sorption of several organic phosphates were measured on soil, peat and other organic and inorganic materials. The behavior of the phosphates on these materials differed from that reported for similar studies on acidic soil materials. In contrast to the sorption on acidic soils, where sorption maxima occur, the sorption on basic soils may reach a maximum but does not decline thereafter. Both clay and organic matter content govern the amount of sorption but calcium seems to account for the differences observed from those on acidic soil materials     

Cadmium sorption by two acid soils as affected by clearing and cultivation

Abstract

The objective of this study was to determine the effect of clearing and cultivation on the sorption of cadmium (Cd) by two acid soils from Zimbabwe with differing cultivation stories. In their original state, not cleared‐not cultivated (virgin soils), the two soils exhibited noticeable and similar capacities to sorb Cd. The Mazowe soil contains the highest level of organic matter (40 g kg^‐1) and a effective cation exchange capacity (ECEC) of 144 mmol_c kg^‐1. Yet, Bulawayo soil (23.5 g kg^‐1 organic matter and ECEC of 146 mmol_c kg^‐1) has higher pH and Mn and Fe oxide content and these characteristics seemed to counteract the effect of lower organic matter. After 50 years of cultivation, The Mazowe soil has lost 60% of its organic matter and ECEC, and consequently the ability of its soil matrix to bind Cd has proportionally decreased. In Bulawayo (cleared in 1983 and first ploughed in 1984), on the contrary, the organic matter and ECEC of the cultivated soil remains over 95% of the values on its virgin counterpart. In this soil, the retaining ability for Cd has not still been affected. In the two soils Cd sorption was highly pH‐dependent. The extent of sorption was minimal under acidic conditions and increased sharply as the pH was raised. The immediate reversibility of the sorption process proved to be very low. When sorption and desorption data were compared it was clear that soil characteristics like high organic matter and oxide content which showed to enhanced Cd sorption, contributed at the same time to slow down the backward reaction.     

Influence of pH on copper, lead and cadmium binding by an ombrotrophic peat

The effect of pH on the adsorption of copper (Cu), lead (Pb) and cadmium (Cd) by a peat soil was studied, and the results compared with those corresponding to cation binding by a dissolved peat humic acid (HA), and interpreted with a NICA–Donnan model. A potentiometric titration technique was used to determine the adsorption isotherms for H⁺, at different ionic strengths, and for Cu²⁺, Pb²⁺ and Cd²⁺ at different pH values, in a peat soil. The effect of the ionic strength on proton binding was similar for the soil (solid) organic matter and for dissolved HA. The adsorption isotherms for cation–peat and the binding curves cation–dissolved HA are almost parallel, although more cation was adsorbed per kg of C in the dissolved HA. The effect of pH on cation binding is similar for dissolved organic matter and for the organic soil. At low metal concentration the amount of adsorbed metal followed the order Cu²⁺ > Pb²⁺ > Cd²⁺. The cation-binding parameters obtained with the NICA–Donnan model allow excellent simulation of the effect of pH on the adsorption of Cu, Pb and Cd ions in the studied peat soil. The binding constants for the peat suspension were greater than the corresponding generic parameters for dissolved HA. Speciation calculations showed that for Cu and Pb, the most abundant fraction was the metal adsorbed on peat, whereas for Cd the most abundant fraction was dissolved metal.     

Influence of organic matter and pH on bentazone sorption in soils

Bentazone (3-isopropyl-1H-2,1,3-benzonthiadiazain-(4)3H-one 2,2-dioxide) is a postemergence herbicide which is used extensively worldwide, especially in China. The sorption of bentazone in various types of soils and extracted humic acids was investigated using a batch equilibration technique. Significant linearity was observed in sorption isotherms in five different types of soil, with distribution coefficients (K(d)) that varied between 0.140 and 0.321 mL g(-1). The distribution coefficient was determined to be a function of organic matter and pH in the soil. A model based on distribution coefficients was developed to predict bentazone sorption in soils. The organic matter-normalized partition coefficients for the neutral and anionic forms of bentazone were 370.3 and 2.40 mL g(-1), respectively. Hence, more attention should be given to the potential leaching problem when bentazone is applied in soils containing low organic matter and high pH.