山东省不同地形区降雨侵蚀力时空变化特征

掌握降水及降雨侵蚀力的时空分布和演变特征对于揭示区域气候变化规律,有效预防和科学评估水土流失等环境问题具有重要意义。基于34个气象站点1961—2015年的降水日值数据,采用降雨侵蚀力计算模型、Mann-Kendall检验、小波分析和Kriging空间插值等研究方法,分析研究了山东省内山地、丘陵和平原等不同地形区的降水和降雨侵蚀力时空变化特征。结果显示：近55年间,全省及各地形区的降水量和降雨侵蚀力均呈波动下降趋势,年内分配均集中在夏季,降雨侵蚀力在时间尺度上存在25年左右的变化周期。空间上,降水和降雨侵蚀力均呈现鲁中南山区＞胶东半岛丘陵区＞鲁西北平原区;分界线由东北至西南沿福山—莱阳—淄博—定陶等站呈“S”型贯穿山东省,界线东南侧降雨侵蚀力高,西北侧降雨侵蚀力较低。其原因主要是受海拔和地形的影响,东南季风携带湿润气流受胶东半岛丘陵及鲁中南山地的阻挡抬升,致使“S”型分界线东南侧迎风面降水及降雨强度相对较高;西北侧背风面形成焚风效应,降水及降雨侵蚀强度较低。该结果可为山东省水土流失空间特征分析奠定数据基础,同时为区域水土资源利用与调控及生态环境保护与改善提供决策支撑。     

Effects of selected pesticides on Rhizobiummeliloti, and on seed germination and Verticillium wilt pathogens of alfalfa

Studies on the effects of 21 fungicides and five pyrethroid insecticides on growth of $\text{Rhizobium}$$\text{meliloti}$, emergence and survival of alfalfa seed and the efficacy of the chemicals in control of Verticillium wilt pathogens were conducted.     

湖沼钉螺孳生环境分布的遥感调查研究

以试验区不同环境类型洲滩钉螺螺情与环境因子进行了调查分析，利用遥感图像编制地貌类型图，土壤类型图和土地利用类型图，在地理相关分析与主导因素分析基础上采取多图件逐步套合方法，以土地利用类型图为主，结合地面钉螺抽样调查和钉螺被动扩散等非遥感信息进行多信息复合，编制了试验区钉螺孳生环境分布图。     

Effect of copper on the adsorption of p-nitrophenol onto soils

The effect of copper on adsorption of p-nitrophenol on two typical Chinese soils was investigated using a batch-equilibration method. Adsorption experiments were carried out when both copper and p-nitrophenol were adsorbed simultaneously, and when copper was previously adsorbed on soils. It was observed that adsorption of p-nitrophenol decreased with increasing copper concentrations thereby indicating a competition between copper and p-nitrophenol for occupying the adsorption sites on soils. Moisture increased the hydrated sphere and the acidity of water surrounding the cation, which further reduced the adsorption of p-nitrophenol. Fourier transform infrared spectroscopy study provided the direct evidence for the coordination of p-nitrophenol sorbed by soils with metal cation in n-hexane system. It was observed that the perturbations included a red shift of the nu(asym) (NO) band, a concomitant blue-shift of the nu(sym) (NO) band and a blue-shift of C-N band when compared with the infrared spectra obtained from water solution.     

北京地铁岛式站台噪声的初步研究

为研究北京岛式站台噪声水平及噪声特点,选取了北京地铁2号线和5号线的10个岛式站台进行了实地的测量,从噪声级以及频谱角度对测量结果进行了分析。结果显示,测量时间内的LAeq,max都高于标准限值80dB(A)。使用独立样本t检验的结果得出,2号线与5号线在LAeq以及LAeq,max上不存在显著差异(P>0.05),说明2号线和5号线噪声在相近的水平上。通过噪声频谱的时程曲线也直观的得出列车在进出站过程中噪声级大于80dB(A),无列车通过且不受相反轨道列车影响时的背景噪声在65dB(A)左右,受影响时在70dB(A)左右。倍频程频谱分析得出,地铁站台噪声具有明显的中频特征。进一步分析,2号线和5号线站台都存在若干的主频,其基频和谐频分别为63、250和1kHz。     

用连续提取法研究芘在鱼鳃表面的结合形态

建立了研究鱼鳃表面芘的结合状态的四步连续提取方法．分别用H2O、CaCl2、CH3OH和n-C6H14+CH2Cl2(1:1, v/v)混合液提取经暴露的鱼鳃．操作定义的前3步分别提取松散附着在鳃表的鱼鳃黏液中的芘,紧密附着在鳃表的鱼鳃黏液中的芘以及直接吸着在鱼鳃表皮上的芘,第4步则用来提取鱼鳃组织吸收的芘．其提取的芘分别占总量的 4．0％、12．1％、45．2％和38．7％．经3 h暴露,进入鳃组织的芘仅为总测定量的三分之一强,因此大部分芘并未进入鳃组织．单独进行的五步CH3OH连续提取实验结果证明,CH3OH提取步骤能有效地解吸鳃表吸着的芘,但不会导致鳃组织中芘的释放．动态实验结果表明,黏液结合态芘在暴露1h左右即达到平衡,而鳃表吸着态和鳃组织吸收态芘在暴露3h内含量迅速上升,3 h后显著趋缓．     

邻苯二甲酸丁基苄酯对小鼠睾丸能量代谢相关酶的影响

为了从生殖细胞能量代谢角度探讨邻苯二甲酸丁基苄酯(BBP)对雄性小鼠生殖损伤的机制,以昆明系雄性小白鼠为实验对象,研究了BBP对小鼠睾丸组织能量代谢相关酶的影响.实验设0、125、250、500、1000mg·kg-1(质量分数)5组浓度梯度,连续灌胃染毒30d后,采用分光光度法检测小鼠睾丸组织匀浆中乳酸脱氢酶(LDH)、琥珀酸脱氢酶(SDH)、Ca-Mg-ATPase酶的活性以及睾丸脏器系数.结果发现,1)与对照组相比,高浓度染毒组(500、1000mg·kg-1)LDH、SDH和Ca-Mg-ATPase活性均极显著降低(p<0.01);而低浓度染毒组(125mg·kg-1)3种酶活性均无显著变化(p>0.05);中浓度染毒组(250mg·kg-1)LDH没有显著变化(p>0.05),而SDH、Ca-Mg-ATPase均显著降低(p<0.05,p<0.01).2)染毒30d后,各染毒组睾丸脏器系数略有下降,但与对照组相比,差异均未达到显著水平(p>0.05).以上结果表明,较高水平的BBP不仅可以干扰睾丸组织有氧代谢及无氧代谢的产能过程,还可以干扰生殖细胞对能量的利用,提示能量代谢的障碍可能是BBP对雄性生殖细胞产生损伤的原因之一.     

Speciation and fractionation of heavy metals in soil experimentally contaminated with Pb,Cd, Cu and Zn together and effects on soil negative surface charge

Speciation and fractionation of heavy metals in soil subsamples experimentally loaded with Pb, Cd, Cu and Zn in orthogonal design was investigated by sequential extraction, and operationally defined as water-soluble and exchangeable(SE), weakly specific adsorbed( WSA),Fe and Mn oxides-bound(OX) and organic-bound( ORG). The results showed that fractions of heavy metals in the soil subsamples depended on their speciation. About 90% of Cd and 75% of Zn existed in soil subsamples in the SE fraction. Lead and Cu existed in soil subsamples as SE, WSA and OX fractions simultaneously, although SE was still the major fraction. Organic-bound heavy metals were not clearly apparent in all the soil subsamples. The concentration of some heavy metal fractions in soil subsamples showed the good correlation with ionic impulsion of soil, especially for the SE fraction. Continuous saturation of soil subsamples with 0.20 mol/L NH4CI, which is the first step for determination of the negative surface charge of soil by the ion retention method, resulted in desorption of certain heavy metals from the soil. It was found that the percentage desorption of heavy metals from soil subsamples depended greatly on pH, the composition and original heavy metal content of the soil subsamples. However, most of the heavy metals in the soil subsamples were still be retained after multiple saturation. Compared with the parent soil, the negative surface charge of soil subsamples loaded with heavy metals did not show difference significantly from that of the parent one by statistical analysis. Heavy metals existed in the soil subsamples mainly as exchangeable and precipitated simultaneously.     

Effect of organic acids on adsorption and desorption of rare earth elements

Effect of citric, malic, tartaric and acetic acids on adsorption of La, Ce, Pr and Nd by and desorption from four typical Chinese soils was studied. Generally, adsorption capacities of rare earth elements (REEs) were significantly correlated with the cation exchange capacity (CEC) of soils. In the presence of acetic acids adsorption of REEs was similar to that in the presence of Ca(NO3)2. However, in the presence of citric, malic and tartaric acids adsorption of REEs by Heilongjiang, Zhejiang and Guangdong soils decreased to varying extents if compared with that in the presence of nitrate and acetic acid. The significance of suppression followed the order of citric acid > malic acid > tartaric acid > acetic acid, which was consistent with the order of stability of complexes of REEs with these organic acids. However, the adsorption increased with increasing equilibrium solution pH. For Jiangxi soil with low soil pH, CEC and organic matter these organic acids exerted an even more serious suppression effect on the adsorption of REEs. Another feature of the relationship between the adsorption of REEs and equilibrium solution pH was that the adsorption of REEs decreased with increase of pH from 2 to 4.5 and then slightly increased with further increase of pH. Desorption of REEs varied with soils and with organic acids as well. REEs were released easily from Heilongjiang, Zhejiang and Guangdong soils in the presence of organic acid. Generally, desorption of REEs decreased with increasing equilibrium solution pH. Effect of organic acids on desorption of REEs from Jiangxi soil was more complicated. In the presence of citric and malic acids no decrement and/or slight increase in desorption of REEs were observed over the equilibrium solution pH from 3 to 6.5. The reasons for this were ascribed to the strong complexing capacity of citric and malic acids and low soil pH, CEC and organic matter of Jiangxi soil.     

Comparison of a rhizosphere-based method with other one-step extraction methods for assessing the bioavailability of soil metals to wheat

There is no method recognized as a universal approach for evaluation of bioavailability of heavy metals in soil. Based on the simulation of the rhizosphere soil conditions and integration of the combined effects of root-soil interactions as a whole, a rhizosphere-based method has been proposed. Wet fresh rhizosphere soil was extracted by low-molecular-weight organic acids (LMWOAs) to fractionate metal fractions of soil pools, which were then correlated with the metal contents of wheat roots and shoots. The rhizosphere-based method was compared with other one-step extraction methods using DTPA, EDTA, CaCl2, and NaNO3 as extractants and the first step of the Community Bureau of Reference (BCR) method. Simple correlation and stepwise multiple regression analysis were used for the comparison. Simple correlation indicated that the extractable Cu, Zn, Cr, and Cd of soils by the rhizosphere-based method were significantly correlated with the metal contents of wheat roots. For DTPA, BCR1 and EDTA methods there was a relatively poor correlation between the extractable Cu, Zn and Cd of soil and metal contents of wheat roots. Stepwise multiple regression analysis revealed that the equation of the rhizosphere-based method was the simplest one, and no soil properties variables needed to be added. In contrast, the equations of other one-step extraction methods were more complicated, and soil properties variables needed to be entered. The most distinct feature of the rhizosphere-based method was that the recommended method was suitable for acidic, neutral and near alkaline soils. However, the DTPA and EDTA extraction methods were suitable for calcareous soils only-or-only for acidic soils. The CaCl2, and NaNO3 extraction methods were only suitable for exchangeable metals. In short, the rhizosphere-based method was the most robust approach for evaluation of bioavailability of heavy metals in soils to wheat.