铁在苹果树器官中的定量研究

成龄苹果树整株分析结果表明 ,果实、叶片、枝干、根系的鲜重分别占整株鲜重的 42 .0 9%、6 .33%、38.81%、12 .77% ,以果实占鲜重的比例最大 ,单株鲜重为 2 0 7.90kg ;果实、叶片、枝干、根系的干重分别占整株干重的 19.5 1%、6 .45 %、5 7.30 %、16 .75 % ,以枝干占干重的比例最大 ,单株干重 84.37kg ,单株含水量 12 3.5 5kg。铁浓度以直径 <0 .5cm的根最高 ,达 2 5 7.5 1mg/kg ,其次为叶片 ,达 2 14.0 9mg/kg ,果实中铁浓度最低 ,为 18.2 7mg/kg;单株总铁含量 4915 .78mg,叶、果、根、枝干中铁含量分别为 116 4.6 5、30 0 .72、15 0 0 .30、1949.6 0mg ,分别占单株总铁量的2 3 .70 %、6 .12 %、30 .5 2 %和 39.6 6 %。     

靠接换砧矫治枳砧甜橙缺铁黄化研究

靠接红桔、酸桔和枸头橙砧,矫治枳砧甜橙缺铁黄化有明显效果。其中,以枸头橙效果最好,以下依次为酸桔和红桔,靠接砧苗后树势逐年恢复,产量成倍增加,靠接红桔、酸桔和枸头橙分别比对照增产3.3、1.4和1.5倍;对提高果实含糖量、果汁率和降低含酸量亦有良好效果。     

山楂缺铁黄叶病及应用硝黄铁防治研究

根据调查初步总结出山楂缺铁黄叶病的发生发展规律、致病因素及其对山楂生产的危害。用新研制的高效价廉、储运方便的硝黄铁矫治,效果明显。黄化病株复绿率40%～87%,三级病株减少36%～100%,叶绿素含量提高64%～224%,喷肥区比对照区株产提高25%。同时增加了果实中糖、酸、果胶及钙、铁含量,提高了果实品质。     

铋系氧化物在光催化技术中的研究进展

总结近年铋系列半导体光催化剂的制备、种类和光催化反应机理等的研究进展,并展望了铋系列半导体光催化剂未来的发展方向.     

非对称扰动下热轧铝带跑偏过程三维数值模拟

基于大型工程分析软件MSC.Marc，设计了模拟Fi机架轧制过程的三维有限元模型，结合实验研究得到的1235铝合金高温本构方程，模拟出非对称性扰动下,热轧铝合金板带跑偏状态；研究了板带在来料厚度分布横向非对称、辊缝形状横向非对称及来料不对中扰动下，轧制力、板带运动轨迹等轧制参数的横向非对称性；探讨了板带跑偏与轧制力、压下率等轧制参数的横向分布特征的相关性.研究结果表明：不同扰动下板带的跑偏方向与两侧轧制力差的关系并不一致，不能根据轧制力差判断板带的跑偏方向；压下率差与跑偏方向具有一致性，板带由压下率大的一边向压下率小的一边跑偏，这一规律为无法明确扰动的板带纠偏策略提供了理论参考.     

兔出血症-巴氏杆菌病铝胶二联灭活苗的研制

筛选了具有良好免疫原性的兔瘟强毒株GMH881和兔巴氏杆菌C51-17株,研制出了兔出血症-巴氏杆菌二联铝胶灭活苗,对疫苗进行了免疫剂量、免疫产生期、兔出血症抗体测定、免疫保护期、保存期等试验;确定出二联铝胶苗免疫剂量1.0 mL;二联铝胶苗在免疫后7 d对兔病毒性出血症强毒的保护率达到100%,二联苗免疫后10～14 d对兔巴氏杆菌的保护率均达到75%以上;二联铝胶苗的兔病毒出血症抗体测定结果表明：二联铝胶苗免疫家兔后7 d,HI抗体均可达25.0,15 d明显上升,二联苗HI效价60～90 d达到最高峰,最高可达210,二联苗在120～180 d仍可维持在27.0～29.5水平。二联铝胶苗分别在免疫后4个月、6个月用兔出血症强毒攻击均产生100%保护,在6个月用2个MLD的兔巴氏杆菌攻击保护率可达70%以上,二联铝胶苗4～8℃条件下保护期暂定为1年,25℃条件下暂定为半年。     

土壤交换性铝的三种测定方法比较

为了准确高效地检测土壤交换性铝含量,探寻适宜的检测方法。比较分析了氯化钾交换-中和滴定法、铝试剂法和羊毛铬花青R比色法所测交换性铝的差异性、精密度、准确性和适用性。结果表明,3种方法所测交换性铝无显著性差异。但羊毛铬花青R比色法的精密度优于氯化钾交换-中和滴定法和铝试剂法,羊毛铬花青R比色法平均回收率达99.28%,准确性高于另2种方法。羊毛铬花青R比色法的线性范围在0~0.32 mg/L,对应吸光值范围在0~0.778;铝试剂法的线性范围在0~0.8 mg/L,对应吸光值范围在0.006~0.157;与铝试剂法相比,羊毛铬花青R比色法的线性范围小于铝试剂法,但其吸光值范围大于铝试剂法。羊毛铬花青R比色法显色剂与显色物质吸收峰间隔较远,测定背景干扰小,方法灵敏度较高。羊毛铬花青R比色法检测单个样品的平均用时为4.2 min,检测效率高于另2种方法,且操作简捷,适用性较高。因此,推荐羊毛铬花青R比色法为土壤交换性铝的测定方法。     

Predicting the degree of phosphorus saturation using the ammonium acetate–EDTA soil test

As a result of the important role played by phosphorus (P) in surface water eutrophication, the susceptibility of soils to release P requires evaluation. The degree of phosphorus saturation, assessed by oxalate extraction (DPS_ox), has been used as an indicator. However, most laboratories do not include DPS_ox in routine soil tests because of cost and time. This study evaluates the suitability of the ammonium acetate extraction in the presence of EDTA (AAEDTA), the standard soil test P (STP) in Wallonia (Southern Belgium), to predict DPS_ox; we also compared it with the Mehlich 3 extraction. Ninety‐three topsoil samples were collected in agricultural soils throughout Wallonia. Good correlations were found between the AAEDTA and the Mehlich 3 methods for P, Fe and Al (r = 0.85, 0.77 and 0.86, respectively). An exponential relationship was found between P_AAEDTA and DPS_ox. Results of principal component analysis and regression demonstrated that STP can be used to predict DPS_ox (r = 0.93) after logarithmic transformation. Soil test Al was also a good indicator of the P sorption capacity (PSC_ox) of soils (r = 0.86). Including the clay fraction in regression equations only slightly improved the prediction of PSC_ox (r = 0.90), while other readily available data (such as pH or organic carbon) did not significantly improve either DPS_ox or PSC_ox predictions.     

Contribution to the study of the podsolisation process

Abstract

Analytical data for Al and Fe extracted by different reagents is presented. It is concluded from the data that in podsolisation Al migrates mainly as inorganic gel while iron moves as organic chelated complexes.     

Evaluation of Commercial Fe(III)‐Chelates Using Different Methods

Abstract

A collaborative assay among three laboratories was made in order to compare both the ion (CEN. EN 13368‐2:2001 E. Determination of chelating agents in fertilizers by ion chromatography. Part 2: EDDHA and EDDHMA, 2001a) and the ion‐pair (Lucena, J.J.; Barak, P.; Hernandez‐Apaolaza, L. Isocratic ion‐pair high‐performance liquid chromatographic method for the determination of various iron(III) chelates. J. Chromatogr. A 1996, 727, 253–264) high performance liquid chromatography (HPLC) methods as well as the soluble and complexed Fe (CEN. EN 13366:2001 E. Treatment with a cation exchange resin for the determination of the chelated micronutrient content and of the chelated fraction of micronutrients, 2001b) methods. Fifteen and ten samples of commercial fertilizers of Fe‐EDDHA, Fe‐EDDHMA, respectively were analysed by three laboratories using these methods. No significant differences were observed between the results obtained for the Fe‐EDDHA content using the Lucena et al. or CEN method. The first method makes it possible to distinguish between the meso and DL‐racemic diasteroisomers of Fe‐o, o‐EDDHA. For the Fe‐EDDHMA formulations, the CEN method gives higher values than the ion‐pair method, since in the first one Fe‐EDDH4,6MA coelutes with FeEDDHMA. Also the CEN method does not makes it possible to distinguish between Fe‐EDDHMA and Fe‐EDDH5MA products. The variability among laboratories was larger for the CEN method than for the Lucena et al. method.