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31.
土霉素是四环素类抗生素中使用较为广泛的一种,探索土霉素在土壤中的吸附解吸规律对抗生素环境风险评价与污染控制具有重要的理论与现实意义。通过改变土壤水溶液中离子强度及类型研究其对土霉素在草甸土中吸附的影响,以期为评价该种抗生素对草甸土土壤环境风险提供科学依据。土霉素测定方法选择高效液相色谱法。以V(乙腈)∶V[NaH2PO4(0.01mol·L-1)]=25∶75为流动相,在流速为1 mL·min-1,检测波长为355 nm条件下进行测定。试验以OECD Guideline 106为基础,采用批平衡法研究不同离子强度(0.01、0.03、0.05、0.08、0.10 mol·L-1CaCl2溶液)和不同阳离子(0.01 mol·L-1的NaCl、KCl、MgCl2溶液)对土霉素在草甸土中的吸附影响。结果表明:随着CaCl2浓度的增加,土霉素在草甸土中的吸附量呈降低趋势,且不同浓度的土霉素在草甸土中吸附量受离子强度的影响是不同的。土霉素浓度较低时,其在草甸土中吸附能力受离子强度影响较土霉素浓度高时小。以土壤吸附系数Kd衡量土壤吸附抗生素能力,当土壤样品中离子强度增大时,其对应Kd值呈非线性趋势减小。这说明,在某一Ca2+浓度范围内,其对吸附的影响较其他浓度范围要大。对相邻CaCl2浓度处理得出的Kd值进行t检验,在CaCl2溶液浓度在0.01与0.03 mol·L-1间得出的Kd值存在显著性差异(p≤0.05),在0.03、0.05、0.08、0.10 mol·L-1浓度间得出的Kd值均没有显著性差异(p〉0.05)。这一结果说明当CaCl2溶液浓度在0.01~0.03 mol·L-1时,其对土霉素在草甸土中的吸附影响较其他浓度范围大。以Freundlich方程对NaCl、KCl、MgCl2溶液条件下土霉素在草甸土中的吸附进行拟合,土样lg Kf值为lg Kf(Mg2+)0.05)。这说明,不同阳离子对土霉素在草甸土上的吸附量(lg Kf)影响的差异并不显著。 相似文献
32.
青藏高原希夏邦马冰芯中阴阳离子的研究 总被引:6,自引:0,他引:6
本文对希夏邦马浅冰芯的资料进行了分析,发同离子含量变化显示强烈的周期性变化,反映了季节变化的特征。离子浓度高低变化将指示气候的冷暖变化。并与降水量变化有着反相关关系,与δ^18O存在着对应关系,但δ^18O对气候变化的反映没有各咱郭反映灵敏。 相似文献
33.
Cations in soil are essential for the growth of plants and micro-organisms. Their availability is dependent on soil organic matter. Soil organic matter (SOM) is heterogeneous comprising amino, aliphatic and phenolic acids, but particularly humic substances. All these substances can complex cations selectively. Mechanisms of complexation with dissolved organic matter are discussed. Such complexation can lead to the apparently contradictory observations that dissolved organic matter (DOM) can either increase the concentration of some less soluble nutrients, making them more available for plant uptake, or make them less available and hence less toxic. the importance of DOM is discussed in relation to soil solution, particularly the rhizosphere, and also in relation to aquatic systems. the latter systems contain mainly dissolved humic substances whereas in the soil, non-humic substances assume a greater importance.
SOM in the rhizosphere is derived from plant, microbial and animal remains but much, especially the water-soluble compounds, are acquired through root exudation. Exudation has important consequences for enhanced nutrient availability as a result of the production of non-humic substances such as amino, aliphatic and phenolic acids. in future, the role of root exudation in relation to DOM and nutrient availability should be investigated more fully, particularly as predicted elevated CO2 levels are likely to have a major impact on root exudation, nutrient availability, and possibly ecosystem community structure and functioning. It is likely that more information will become available on aquatic systems as more highly sensitive techniques and equipment capable of dealing with low concentrations of DOM in these systems become available. 相似文献
SOM in the rhizosphere is derived from plant, microbial and animal remains but much, especially the water-soluble compounds, are acquired through root exudation. Exudation has important consequences for enhanced nutrient availability as a result of the production of non-humic substances such as amino, aliphatic and phenolic acids. in future, the role of root exudation in relation to DOM and nutrient availability should be investigated more fully, particularly as predicted elevated CO2 levels are likely to have a major impact on root exudation, nutrient availability, and possibly ecosystem community structure and functioning. It is likely that more information will become available on aquatic systems as more highly sensitive techniques and equipment capable of dealing with low concentrations of DOM in these systems become available. 相似文献
34.
The existence of electrolytes in aquatic environment on the photocatalytic performance and coagulation of nanodispersed TiO2 hydrosol and the corresponding photocatalytic alteration were investigated by studying cations (Na+, K+, Ca 2+, Mg2+, and Al3+). The photocatalysis reactions of nano TiO2 with different dosages of electrolytes were measured by monitoring the degradation of Rhodamine B (RhB) under ultraviolet A (UV-A) irradiation over time. The results showed that the photocatalytic performance of TiO2 was improved by the presence of Al3+, while the performance was impaired by the other tested cations. The negative influences of divalent ions on the photocatalytic performance of TiO2 were more significant than monovalent ions. The TiO2 sol dispersed stable at nano scale at low concentration of electrolyte (< 0.01?mol/L) with slight change of pH, and coagulated into micro sizes at high concentration of electrolytes (> 0.1?mol/L) with larger increase or decrease of pH. The positive effects of Al3+ on the photodegradation rate of RhB might relate to the strong hydrolytic action of Al3+ in aquatic solutions. The photocatalytic processes of TiO2 in the presence of all ions followed the Langmuir-Hinshelwood model, and the reaction kinetic constant was increased with the decrease of pH caused by different cations. These work suggested a new perspective about the relationship between coagulation and photocatalytic performance of TiO2 hydrosols in electrolyte with hydrolysable cations, which demonstrated that TiO2 hydrosols may be suitable as photocatalysts in aquatic environments. 相似文献
35.
Occurrence of Acid Rain over Delhi 总被引:1,自引:0,他引:1
Precipitation samples were collected as wet-fall only andprimarily on event basis in Delhi during the monsoon period of1995. Concentrations of major anions (SO4
2-,NO3
- and Cl-) andcations (Ca2+, Mg2+,Na+ and K+) were determined. The pH of the rain waterwas found to be more than 5.6, showing alkalinity during theearly phase of monsoon, but during the late phase of monsoon pHtendency was towards acidity due to lack of proper neutralizationof acidic ions. Neutralization is not only due to the localprocess but also due to the pre-monsoon Andhi which bringsSuspended Particulate Matter (SPM) containing Ca2+,Mg2+, Na+ and K+ as well as the local emission ofNH3. In the late monsoon the concentration of cations getsreduced because of heavy rainfall and relatively unfavourablecondition for their transport from the adjoining areas, whereasthe anion concentrations remain unchanged owing to theircontinuous emission. 相似文献
36.
本文综述了高效液相色谱法在无机分析中的应用进展。分别介绍了正相、反相、离子对、离子交换、排阻和胶束流动相等液相色谱法在有机金属化合物、金属络合物、无机阳离子和阴离子分离及测定上的实际应用。 相似文献
37.
Veni Pillay Sreekanth B. Jonnalagadda 《Journal of environmental science and health. Part. B》2013,48(4):423-428
The total concentration of toxic elements (aluminum, cadmium, chromium and lead) and selected macro and micro elements (iron, manganese, copper and zinc) are reported in six leafy edible vegetation species, namely lettuce, spinach, cabbage, chards and green and red types of Amaranth herbs. Although spinach and chards had greater than 125 mv of iron, both the amaranthus herbs recorded > than 320 μ g g? 1 dry weight. In both the spinach and chard species, the Mn and Zn levels were appreciable recording > 225 μ g g? 1 and 150 μ g g? 1 dry weight, respectively. Aluminum concentrations were (in μ g g? 1 dry weight) lettuce (10), cabbage (11), spinach (167), chards (65), amaranthus green (293) and amaranthus red (233). All the micro and macro elements and the toxic elements (Ni, Cr, Cd and Pb) elements analyzed, were below the recommended maximum permitted levels (RMI) in vegetables. Further the elemental uptake and distribution of the nine elements, at three growth stages of the lettuce plant grown on soil bed under controlled conditions are detailed. In the soil, except for iron (16%), greater than 33% of the other cations were in exchangeable form. Generally in the lettuce plant, roots retained much of the iron (> 224 μ g g? 1) and aluminum (> 360 μ g g? 1), while leaves had less than 200 μ g g? 1 of iron and 165 μ g g? 1 of Al. Although the concentrations of elements marginally decreased with growth, the lettuce leaves had significant amounts of Mn (30 μ g g? 1), Zn (50 μ g g? 1) and Cu (3.6 μ g g? 1). Some presence of lead in leaves (2.0 μ g g? 1) was noticed, but all the toxic and other elements analyzed were well below the RMI values for the vegetables. 相似文献
38.
Cations in soil are essential for the growth of plants and micro-organisms. Their availability is dependent on soil organic matter. Soil organic matter (SOM) is heterogeneous comprising amino, aliphatic and phenolic acids, but particularly humic substances. All these substances can complex cations selectively. Mechanisms of complexation with dissolved organic matter are discussed. Such complexation can lead to the apparently contradictory observations that dissolved organic matter (DOM) can either increase the concentration of some less soluble nutrients, making them more available for plant uptake, or make them less available and hence less toxic. the importance of DOM is discussed in relation to soil solution, particularly the rhizosphere, and also in relation to aquatic systems. the latter systems contain mainly dissolved humic substances whereas in the soil, non-humic substances assume a greater importance. SOM in the rhizosphere is derived from plant, microbial and animal remains but much, especially the water-soluble compounds, are acquired through root exudation. Exudation has important consequences for enhanced nutrient availability as a result of the production of non-humic substances such as amino, aliphatic and phenolic acids. in future, the role of root exudation in relation to DOM and nutrient availability should be investigated more fully, particularly as predicted elevated CO2 levels are likely to have a major impact on root exudation, nutrient availability, and possibly ecosystem community structure and functioning. It is likely that more information will become available on aquatic systems as more highly sensitive techniques and equipment capable of dealing with low concentrations of DOM in these systems become available. 相似文献
39.
Kuo Fang Fei Peng Hui Gong Huanzhen Zhang Kaijun Wang 《Frontiers of Environmental Science & Engineering》2021,15(1):8
40.
Howard D. Passell Clifford N. Dahm Edward J. Bedrick 《Journal of the American Water Resources Association》2004,40(1):111-127
ABSTRACT: Hydrological and geochemical spatial patterns and temporal trends were analyzed using U.S. Geological Survey (USGS) water quality data collected from 1975 to 1999 along the uppermost 600 km of the Rio Grande in Colorado and New Mexico. Data on discharge, specific conductivity (SC), total dissolved solids (TDS), pH, Ca2+, Na+, Mg2+, K+, HCO3?, SO42‐, Cl?, F?, and SiO2 came from six USGS stations ranging from the Colorado‐New Mexico border to below Albuquerque, New Mexico. Linear regression, Kendall's S, and Seasonal Kendall's S’ were used to detect trends, and ANOVA was used to analyze spatial differences between stations. Statistically significant increasing trends occurred in SC, TDS, Ca2+, Na+, Mg2+, K+, Cl?, and F?in the uppermost reaches, and significant decreasing trends of SC, TDS, Ca2+, Mg2+, K+, HCO3?, and SO42‐occurred at the lower stations around Albuquerque. Both fluoride concentrations and pH values increased at and below Albuquerque over the study period. Discharge data show an increasing trend across all stations. Spatially, data for dissolved substances show generally linear upstream to downstream increases in concentrations in the upper four stations, with several notable nonlinear increases at and below Albuquerque (SC, TDS, Na+, Cl?). Significant increases in pH appear at and below Albuquerque, relative to upstream stations, probably due to improved sewage treatment. 相似文献