不同密度紧凑型油菜的源库特征及与收获指数的相关研究

旨在为油菜株型育种和机械化栽培提供理论和技术依据。选用3个不同类型的紧凑型油菜常规品种,以松散型油菜杂交种‘秦优7号’为对照,研究了在15万、30万、45万、60万、75万、90万株/hm²密度下各品系的库源特征及其与收获指数的关系。结果表明,紧凑型油菜单株在不同密度下的库源特征与对照松散型相同,单株根、茎、枝、壳干重,角粒数和单株角果数随种植密度的增加而降低,且低密度显著高于高密度;千粒重随密度的变化不大。紧凑型油菜的生物学产量和经济产量随种植密度的增加而增加,松散型油菜随种植密度的增加而下降。说明紧凑型油菜适宜密植和机械化收获。收获指数对密度的响应在两类型品种表现一致,最低密度15万株/hm²增加到30万株/hm²时达到峰值,以后随着种植密度的继续增加而降低。收获指数与茎+枝+壳干重之和,与库性状角粒数、角果数、千粒重、单株产量,与库源关系的粒根比、粒茎比、粒枝比、粒壳比显著正相关,说明要提高收获指数不仅要扩“源”增“库”,还要协调库源的合理分配比例。     

保定市一亩泉河河流中COD的变化及污染源分析

针对保定市城区水系管理委员会2017年3月公布的黑臭水体河流中的一亩泉河7.23km的黑臭水体段为参考进行了勘查、取样与COD实验工作,从2019年4月12日到2019年5月29日进行了为期一个半月的时间。研究结果表明:保定市一亩泉河河流不同位置COD大小不同、污染原因不同。通过周围景观的变化、对采样点附近居民进行的走访和COD浓度的测定,对一亩泉河的水质状况和污染源进行了全面系统地分析。并为此提出了切实可行、经济有效、便于管理的控制方案。     

异噻菌胺原药高效液相色谱分析方法研究

本文采用高效液相色谱法,以乙腈+磷酸溶液为流动相,使用ZORBAX SB-C18色谱柱和二极管阵列检测器,在280nm波长下对异噻菌胺原药进行分离和定量分析。结果表明,该分析方法的线性相关系数为1.000 0,标准偏差为0.39,变异系数为0.39%,平均回收率为100.08%。     

2015年华南4种林业期刊引文对比分析

为探讨林业期刊引文特点,对华南4种林业期刊《桉树科技》、《热带林业》、《广东林业科技》和《广西林业科学》2015年度所刊发的论文引文进行引文量、引文率、篇均引文量、引文类型、引文语种、期刊自引率等6个方面进行对比分析,结果表明:2015年4种林业期刊引文量为442 ～1 839条,平均1094条;篇均引文量7.8～16.4条,平均13.6条;除《热带林业》引文率为94.7％外,《桉树科技》等3种期刊引文率均达100％;均以期刊类引文最多,图书类次之,学位论文、标准、专利等其他引文最少,其平均所占比例分别为82.3％、10.3％和7.5％.4种林业期刊的引文语种为中文与英文两种,其所占比例分别为88.7％与11.3％;平均期刊自引率偏低,为4.3％,与我国农业科学类期刊平均自引率9.7％的差距较大.     

土耳其斯坦裂体吸虫23kDa蛋白基因的序列分析及抗原表位预测

为研究土耳其斯坦裂体吸虫23 kDa蛋白的生物学特性,以土耳其斯坦裂体吸虫cDNA为模版,利用PCR对23 kDa基因进行扩增,并将其克隆到T-easy载体后进行序列测定。利用生物信息学对其结构、抗原指数进行分析,并对其抗原表位进行预测。序列分析结果表明,该虫体的23 kDa基因长度为657 bp,A+T含量为57.38%,与曼氏血吸虫、埃及血吸虫和日本血吸虫的23 kDa基因的相似性分别为85.24%、83.71%和81.89%。蛋白二级结构分析表明,23 kDa蛋白经过4次跨膜,主要由6个α-螺旋、3个β-折叠、7个β转角和若干个无规则卷曲构成。抗原表位预测结果表明,该蛋白有3个B细胞抗原表位。综合分析土耳其斯坦裂体吸虫23 kDa蛋白是一种较好的抗原分子,是土耳其斯坦裂体吸虫疫苗的重要候选分子。     

屋面防水的施工要点与整改措施

防水工程一直是建筑施工中难以控制的分项,防水层关系到日后的质量问题,如渗水势必会对房屋的适用性、耐久性造成影响.防水层的试水试验相当重要,也做为检验防水层施工质量的依据,今后施工防水层一定要重视蓄水试验,按照设计及技术方案做好防水层的施工.     

加强农村生活垃圾收集处理 促进可持续发展

通过对该黑龙江省集贤县农村生活垃圾处理情况的调查,深切感到解决农村生活垃圾问题的重要性,对此提出了对策建议     

Nutrient cycling and biomass flows in a low-quality forest stand improvement system in the Lesser Khingan Range of China

The material flow and bulk internal flow analyses were used to establish a material accumulation and cycling model for a low-quality forest stand improvement system and a series of processes were considered. The model was applied in a one-hectare low-quality forest plot in the Lesser Khingan Range of China. Results showed that during 1997–2007, the stands absorbed 270.19 kg of N, 74.28 kg of P, and 124.39 kg of K from soils, 51.82 kg of N and 2.38 kg of P were directly absorbed by foliage, and 16.25 kg of K was released to soils by eluviation. Until 2007, the accumulated nutrients in the stands included 236.91 kg of N, 65.28 kg of P, and 108.55 kg of K. When horizontal strip clearcutting was applied in 2007, 50% accumulated nutrients in the stands were shifted due to harvesting operations, and 212.74 kg of N, 26.97 kg of P, and 98.88 kg of K were accumulated in soils, declining by 9.47% for N, 3.68% for P, and 17.60% for K, respectively, compared with year 1997. 94.61 t per hectare of biomass was generated, of which the biomass in stands accounted for 87.36%. The felled tree biomass was 36.89 t per hectare, of which 84.90% and 10.03% of biomass were utilized in terms of logs and other means, and the rest was left on site.     

Cloning and Sequence Analysis of PTTG1 Gene in Luchuan Pig

This experiment was aimed to clone PTTG1 gene CDS sequence of Luchuan pig,and was analyzed by bioinformatics methods.A pair of special primers was designed according to predicted sequence of porcine PTTG1 in GenBank.The coding sequence of PTTG1 in Luchuan pig was amplified by RT-PCR,its gene sequence characteristics and protein structure was systemically analyzed by bioinformatics techniques.The results showed that the cloned PTTG1 fragment included a 609 bp CDS (coding 202 amino acids).The sequence multi-aligned results showed that Luchuan pig shared 90.15%,87.85%,87.52%,87.03%,76.03%,74.38%,55.74% and 44.48% of similar nucleotide sequence with that of Bos,Pan troglodytes,Homos,Macaca,Rattus,Mus,Gallus and Danio retio,respectively.The protein structure analysis results showed that the protein attributed hydrophilic protein without signal peptide,localized in cell cytoplasm and had 16 phosphorylation sites.The phylogentic tree of amino acid indicated that PTTG1 was highly conserved in the process of evolution of different species.The cloning and analysis of PTTG1 gene provided an important foundation for further study biological function of porcine PTTG1 during early embryonic development.