Subcellular distribution and toxicity of cadmium in Potamogeton crispus L

The submerged macrophyte Potamogeton crispus L. was subjected to varying doses of cadmium (0, 20, 40, 60 and 80 μM) for 7 d, and the plants were analyzed for subcellular distribution of Cd, accumulation of mineral nutrients, photosynthesis, oxidative stress, protein content, and ultrastructural distribution of calcium (Ca). Leaf fractionation by differential centrifugation indicated that 48-69% of Cd was accumulated in the cell wall. At all doses of Cd, the levels of Ca and B rose and the level of Mn fell; the levels of Fe, Mg, Zn, Cu, Mo, and P rose initially only to decline later. Exposure to Cd caused oxidative stress as evident by increased content of malondialdehyde and decreased contents of chlorophyll and protein. Photosynthetic efficiency, as indicated by the quenching of chlorophyll a fluorescence (Fv/Fm, Fo and Fm), decreased significantly, the extent of decrease being directly proportional to the concentration of Cd. Increased amounts of precipitates of calcium were noticed in the treated plants, located either outside the cell membrane or in chloroplasts, mitochondria, the nucleus, and the cytoplasm whereas control plants showed small deposits of the precipitates around surface of the vacuole membrane and in the intercellular space but rarely in the cytoplasm. Photosynthetic efficiency and oxidative stress could be used as indicators of physiological end-points in determining the extent of Cd phytotoxicity.     

Fate and availability of glyphosate and AMPA in agricultural soil

The fate of glyphosate and its degradation product aminomethylphosphonic acid (AMPA) was studied in soil. Labeled glyphosate was used to be able to distinguish the measured quantities of glyphosate and AMPA from the background values since the soil was sampled in a field where glyphosate had been used formerly. After addition of labeled glyphosate, the disappearance of glyphosate and the formation and disappearance of AMPA were monitored. The resulting curves were fitted according to a new EU guideline. The best fit of the glyphosate degradation data was obtained using a first-order multi compartment (FOMC) model. DT₅₀ values of 9 days (glyphosate) and 32 days (AMPA) indicated relatively rapid degradation. After an aging period of 6 months, the leaching risk of each residue was determined by treating the soil with pure water or a phosphate solution (pH 6), to simulate rain over a non-fertilized or fertilized field, respectively. Significantly larger (p < 0.05) amounts of aged glyphosate and AMPA were extracted from the soil when phosphate solution was used as an extraction agent, compared with pure water. This indicates that the risk of leaching of aged glyphosate and AMPA residues from soil is greater in fertilized soil. The blank soil, to which 252 g glyphosate/ha was applied 21 months before this study, contained 0.81 ng glyphosate/g dry soil and 10.46 ng AMPA/g dry soil at the start of the study. Blank soil samples were used as controls without glyphosate addition. After incubation of the blank soil samples for 6 months, a significantly larger amount of AMPA was extracted from the soil treated with phosphate solution than from that treated with pure water. To determine the degree of uptake of aged glyphosate residues by crops growing in the soil, ¹⁴C-labeled glyphosate was applied to soil 6.5 months prior to sowing rape and barley seeds. After 41 days, 0.006 ± 0.002% and 0.005 ± 0.001% of the applied radioactivity was measured in rape and barley, respectively.     

太湖地区“禁磷”措施的效果及在富营养化控制中的作用

通过太湖地区采取“禁磷”措施前后城市生活污水、主要入湖河水和湖体水域中磷浓度与富营养化指数变化的分析 ,证实“禁磷”措施对降低居民生活污水中磷浓度的作用较为明显 ,降幅为 2 4 %左右 ,但对入湖河道和湖体水域中磷浓度与水体富营养化的影响则不明显。表明太湖富营养化的改善 ,除了实施“禁磷”措施外 ,尚需结合流域内其它污染治理措施 ,进行综合治理 ,才能取得较好的效果。     

不同条件下高炉渣吸附水中无机磷的研究

高炉渣(BFS)是在冶炼生铁过程中产生的固体废弃物,开展高炉渣的资源化研究具有重要意义.为了对水淬高炉渣净化含磷污水的应用提供理论依据,采取等温吸附的实验方法,比较了不同水淬炉渣的吸附磷效果,研究了不同pH和不同温度下水淬炉渣吸附磷的特点,结果如下:利用Langmuir等温吸附方程炉渣吸附磷的过程进行拟合,其相关系数均能达到显著水平.炉渣的碱度越高,吸附磷的效果越好;炉渣对磷的吸附能力随溶液pH的增加而降低,且初始为酸性(pH=2、4)的溶液在吸附达到平衡后pH有所上升,而初始为碱性的溶液(pH=10、12)在吸附达到平衡后pH有所下降;炉渣对磷的吸附是一个自发放热过程.     

Potential environmental impact of dissolution of raw phosphate in sea water of the Gulf of Aqaba

Dissolution of raw phosphate (apatite) in sea water of the Gulf of Aqaba was investigated through lab incubation experiments. Three types from three different sources (Al-Hasa, Al-Abyad and Esh-Shydiya) have been used for these experiments. Impact of quantity, grain size, and source (type) of raw phosphate on dissolution rate were studied. Statistical analysis shows significant differences between the results obtained from comparing each two weights; as weight of apatite increased, dissolved inorganic phosphate-phosphorus (DIP) and fluoride in sea water solution increased. The differences between the dissolution rates of raw phosphate from the three sites were not significant while the differences between the different grain size fractions were significant. Dissolution rates were inversely related to particle size. Using a worst-case scenario, a conservative estimate of the maximum increase in DIP in seawater of the Gulf of Aqaba due to the apatite particles lost to the sea during ship loading resulted in DIP concentrations of 0.03 μM per year. As the residence time of the water in the Gulf of Aqaba is about one year, the DIP concentration will not increase by more than 0.03 μM under the estimated annual quantity of exported phosphate. Fluoride will not increase by more than 0.03 mg/l under the same conditions.     

有效磷含量对硝酸铵溶液热安全性的影响

为了了解硝酸磷肥生产过程中,硝酸铵溶液中加入磷酸一铵的安全性,通过自制实验装置,研究了有效磷含量对质量分数为85%的硝酸铵溶液热分解的影响。结果表明,质量分数为85%的硝酸铵和磷酸一铵混合溶液的临界爆炸温度高于纯质量分数为85%的硝酸铵溶液,稳定性更好;磷酸一铵抑制硝酸铵的热分解,随着有效磷含量的增加,硝酸铵混合溶液临界爆炸温度升高;升温速率对硝酸铵混合溶液的临界爆炸温度影响很大,随着升温速率由2℃/min升高到3℃/min,质量分数为85%的硝酸铵混合溶液的临界爆炸温度升高,不易发生爆炸,安全性更好。研究结果对硝酸磷肥的生产安全有一定的指导意义。     

磷酸银/树脂复合物的制备及其对亚甲基蓝的光催化降解

以聚乙烯吡咯烷酮(PVP)为稳定剂,采用化学沉积法制备了磷酸银/树脂复合物,降解亚甲基蓝,研究其光催化活性,并对样品进行了XRD和SEM表征。探讨了不同的光源、催化剂投加量、PVP含量、p H值等因素对亚甲基蓝降解率的影响。结果表明,在太阳光(夏天早上9点到11点的阳光)下,偏酸介质中,催化剂用量为0.8 g/L,PVP质量分数为0.01%的磷酸银/树脂复合物,液面高度为15 cm的条件下对亚甲基蓝有最佳降解效果。     

新型纳米结构铈锰复合氧化物的磷吸附行为与机制研究

采用共沉淀法制备了一种新型铈锰复合氧化物吸附剂,对其进行了表征,并对磷吸附行为与机制进行了研究.表征结果分析表明,此氧化物由纳米级颗粒组成;铈锰复合氧化物中的铈氧化物有类似水合氧化铈的无定形结构;BET比表面积为157 m2·g-1,等电点为6.5.吸附实验结果表明,Langmuir吸附等温线模型可以更好地拟合铈锰复合氧化物对磷的吸附,最大吸附量为28.6 mg·g-1(p H=7.0);铈锰复合氧化物对磷具有较高的吸附速率,更符合准二级动力学模型;溶液p H对铈锰复合氧化物吸附磷的影响较为明显,随p H升高,吸附量降低;离子强度则影响不大;共存阴离子对吸附影响的大小顺序为Si O2-3CO2-3Cl-≥SO2-4.通过对铈锰复合氧化物吸附磷前后Zeta电位和红外谱图(FTIR)分析,可以推断磷在铈锰复合氧化物表面发生了特性吸附,磷酸根主要通过取代复合氧化物表面的金属羟基而被吸附去除.     

Effect of commercial pesticides on plant growth-promoting activities of Burkholderia sp. strain L2 isolated from rhizosphere of Lycopersicon esculentum cultivated in agricultural soil

The in vitro study was carried out to examine the toxicity of four commercially used pesticides (phorate, mancozeb, chlorpyrifos, and endosulfan) at the recommended dose (1X) and higher field doses (1.5X, 2X, 2.5X, and 3X) on plant growth-promoting activities of Burkholderia sp. strain L2, isolated from pesticide-treated rhizosphere of Lycopersicon esculentum. At the recommended dose, level of toxicity of all the pesticides to phosphate solubilization activity and indole-3-acetic acid (IAA) production was less detrimental as compared to exceeding doses. At maximum dose rate of each pesticide, the percentage decrease in phosphate solubilization and IAA production over control was found in order of chlorpyrifos < mancozeb < endosulfan < phorate. Present study proves that Burkholderia sp. strain L2 could be used as a potential microbial inoculant in the agricultural soil having persistent pesticide residues.