小样本情况下需水量预测模型研究

针对传统的GM（1,1）模型,分析了其预测结果与实际过程存在的偏差,通过GM（1,1）模型与自回归滑动平均模型相结合的方法以弥补偏差。以钦州市1999-2009年及2005-2009年城市供水总量这两组基础数据对本文所建模型进行验证,并利用此模型预测了钦州市2010-2018年需水量。通过与其他预测模型的对比,进一步证...     

SSR分子标记检测杂交稻种纯度的技术改良

通过改进DNA提取方法,利用多层点样的电泳技术和样本量确定等方面,探讨SSR分子标记检测杂交稻种纯度技术的改良,以期能提高室内纯度检测的可靠性及效率。结果表明:利用TPS法提取糙米DNA和3层点样的电泳技术是可行的;192~288的样本量较适合室内种子纯度检测。     

The measurements of acid detergent fibre in rapeseed by visible and near-infrared spectroscopy

Visible and near‐infrared spectroscopy (NIRS) calibrations for acid detergent fibre (ADF) in intact rapeseed (Brassica napus L.) were performed for two different sample volumes (10 ml, 500 seeds approximately; and 1 ml, 50 seeds approximately). The inclusion of brown and yellow‐seeded cultivars in this work has allowed the whole range of ADF currently described in the literature for this character to be covered. Chemometric techniques have been used for developing calibration equations for both procedures when measuring the two different seed sample volumes. On the basis of the coefficient of determination in the cross‐validation (R²cv) obtained for the 10 and 1 ml assays (0.80 and 0.73), and SECV/SEL ratios (2.30 and 2.57), respectively, both equations showed an accuracy sufficient for screening purposes in an ADF range from 6.80 to 13.46% dry wt, which is presented in this work.     

环境和食品中阿维菌素类药物残留量检测方法研究进展

阿维菌素类药物是一种常用的杀虫剂,现有报道的食品和环境基质样品中阿维菌素残留分析最为常用的检测仪器为液相色谱-串联质谱。基于此,已建立了一系列的不同样基质中多种阿维菌素类药物残留量的检测方法,本研究除了关注常见的多种阿维菌素残留量的测定方法,也关注了食品和环境样品中单种阿维菌素化合物的专一性检测方法。本研究从阿维菌素在食品和环境领域的应用以及赋存状态、前处理方式（提取和净化方法）、检测方法（液相色谱法、酶联免疫法和液相色谱-串联质谱法）及定量方式和基质干扰等方面,综述了2010—2020年不同检测技术在食品和环境样品基质中阿维菌素类化合物残留分析中的研究与应用进展。最后,综述了多残留量检测方法的局限性,未来的关注点以及对阿维菌素残留分析方法的发展趋势。本研究可为开展烟草中阿维菌素类化合物残留分析技术研究提供参考。     

Determination of Total Ammonium Nitrogen in Pig and Cattle Slurry: Sample Preparation and Analysis

Abstract

In order to supply the correct amount of ammonium to the crop when slurry is spread on the field, it is necessary to know the ammonium concentration. Slurry is a heterogeneous substance and there is a risk that organic N-compounds and the ionic strength will interfere with the determination of ammonium. The usability of five different methods for the determination of ammonium in solution has been tested on 18 different cattle and pig slurries and compared to a manual distillation titration technique. Colorimetric determination using an autoanalyzer and an automatic titration distillation device using MgO were highly accurate, and the precision was close to 1%. Distillation with NaOH caused interference from hydrolysable organic compounds. An ammonium electrode could be used, but the accuracy was not good. When using the automatic titration distillation device, samples should immediately be transferred to Kjeldahl flasks with water or acidified to prevent loss of volatile ammonia, unless they are to be distilled within 30 min.     

联结度指数构造模型及其应用

植物种间联结关系的研究约有 1 0 0年的历史 ,国内外学者提出了多种公式 :I1 =(ad-bc) (ad bc) (Yule ,1 91 2 ) ,I2 =2a (2a b c) (Dice ,1 94 5 ) ,I3 =(a b) (a c) a(Margalef,1 95 8) ,上述这些公式均没有考虑每一样方的种群数量 ,而只检查种是否出现 ;无疑这些指数受     

烟蚜的空间分布型及抽样技术初步研究

作者对陕北烟草上发生的烟蚜进行了空间分布型测定,为聚集分布。求得最适抽样数为N=56.91/x 16.21(三为平均每株有蚜数),当临界防治密度为平均每株有蚜5头时,序贯抽样的上、下限为T(n)=5n±7.88n~(1/2)。     

高效液相色谱法测定土壤中的二氯喹啉酸

用50 ml甲醇︰0.05 mol/L硼砂溶液(p H=10)(9︰1,v/v)作为提取剂对20 g(或适量)土壤样品中残留的二氯喹啉酸振荡提取2 h,离心过滤后分取滤液25 ml浓缩,甲醇定容至2 ml,再用滤膜过滤后待测定;高效液相色谱仪(HPLC)以1.0 ml/min的甲醇︰1%乙酸水溶液(55︰45,V/V)为流动相,柱温45℃,在238 nm的紫外光波长下进行二氯喹啉酸的外标法定量。该方法精密度为6.0%,检出限为0.012 mg/kg,不同类型土壤的加标回收率74.9%~98.8%,能满足有机分析要求。该方法既简捷易操作,又能满足土壤中二氯喹啉酸低残留量的测定。