土壤团聚体有机碳研究进展

土壤有机碳是衡量土壤肥力的重要指标,对于促进土壤养分循环、增加养分有效性有重要作用。土壤团聚体是土壤的重要组成部分,是组成土壤结构的最小单元,受到自然因素和人为因素的影响,其形成转化过程与土壤固碳过程息息相关,因而研究团聚体和有机碳的关系及团聚体有机碳影响因素对于土壤结构的改善和土壤质量的提升具有重要意义。本文通过对文献的总结,明晰了土壤团聚体和有机碳的关系,阐述了土壤类型、施肥方式、土地利用和矿区复垦对土壤团聚体有机碳的影响,并从生物质炭的长期定位研究和复垦矿区的土壤修复两方面对土壤团聚体有机碳的研究进行展望,研究结果可为合理的农业生产提供科学依据。     

不同辣椒种质对象耳豆根结线虫的抗性评价

近年来象耳豆根结线虫的危害日益严重.为筛选抗象耳豆根结线虫的辣椒种质,本试验利用种属特异性引物对根结线虫病原物开展分子鉴定,确定为象耳豆根结线虫.接着采用室内人工接种法,对10份一年生辣椒种质和10份中国辣椒种质进行象耳豆根结线虫抗性鉴定,计算根结指数和卵粒指数,并通过比较隶属函数,发现其中3份辣椒种质对象耳豆根结线虫表现为高抗,抗病性最强的是L518M和L525-1M,L42M次之;10份表现为中抗;7份表现为感病,抗病能力最弱的是L69-1M;未发现免疫品种.本研究发现中国辣椒种质的抗病性整体高于一年生辣椒,是重要的抗病种质来源,可用于象耳豆根结线虫抗病育种和后续抗病机理的研究.     

白屈菜CmFAD2基因的克隆及植物转化载体构建

通过对白屈菜低温应答过程的转录组分析发现膜脂不饱和化相关基因的表达在一定过程中发生变化,脂肪酸去饱和酶基因FAD2在随温度的变化趋势为正"V"型,且表达量变化显著。利用NCBI等在线软件对序列进行相关生物学信息分析,并对白屈菜FAD家族成员FAD2基因的完整开放阅读框(ORF)进行克隆,并命名为CmFAD2。选用克隆载体pMD-19-T,转化大肠杆菌DH5α,测序验证序列正确性及完整性。将目的基因与植物表达载体pRI-201-AN连接构建重组DNA pRI-201-AN-Cm FAD2,电击法转化农杆菌LBA4404,利用菌液PCR法验证成功。该基因可作为药用植物抗寒品种创制的候选基因。     

Dietary Lipid Levels Affect the Growth Performance,Lipid Deposition,and Antioxidative Capacity of Juvenile Scaleless Carp,Gymnocypris przewalskii,on the Qinghai‐Tibetan Plateau

A 56‐d growth trial was conducted to evaluate the growth performance, lipid deposition, and antioxidative capacity of juvenile scaleless carp, Gymnocypris przewalskii, on Qinghai‐Tibetan Plateau. One‐year‐old juveniles (initial weight: 15.99 ± 0.02 g) were fed practical diets with different lipid levels of 4, 5.5, 7, 8.5, and 10%, respectively. Results showed that the best specific growth rate (SGR), feed conversion rate, and total antioxidative capacity (T‐AOC) in hepatopancreas were observed in fish fed the diet with 7% lipid level. Fish fed with high lipid diets (8.5 and 10%) had significantly higher condition factor and viscerosomatic index as well as lipid in muscle, intestine, mesenteric fat tissue, and whole body. Highest level of hepatopancreas lipase and lipoprotein lipases activities as well as malondialdehyde content and the lowest level of feed intake and T‐AOC content in hepatopancreas and intestine were also observed in fish fed with high lipid diets (8.5 and 10%) (P < 0.05). In conclusion, based on SGR and hepatopancreas T‐AOC content, dietary lipid requirement of juvenile G. przewalskii was estimated to be 7.35 and 7.39%, respectively.     

优质国审棉品种——ZHM19

概述了ZHM19的选育过程、特征特性、产量、纤维品质和抗病性等特点及主要栽培技术措施。     

直播稻田无人机全程防治病虫草害初探

针对不同设备设计不同喷液量,飞行参数验证防治效果,从而验证无人机在稻田全程应用的可能性,旨在探索2种小型多旋翼植保无人机低空喷洒在整个水稻生长时期病虫草害防治过程中的防效。结果表明:当喷洒水田封闭式除草剂的喷洒量为10650、15000 mL/hm²,其对杂草的株防效与鲜重防效与人工电动喷雾相近。在病虫害的防治试验中,使用推荐用量且喷洒量为10650、15000 mL/hm²时,以及使用70%推荐用量（减量30%）且喷洒量为15000 mL/hm²时,防治效果均与人工电动喷雾器无显著差异。通过验证,选择合适的药剂,配合科学的喷洒参数,可在保证药效的前提下减少农药使用量。多旋翼植保无人机在水稻田有进行大面积全程飞防植保应用有广阔的前景。     

Effects of natural pyrethrum and synthetic pyrethroids on the tiger mosquito,Aedes albopictus (skuse) and non-target flower-visiting insects in urban green areas of Padua,Italy

Abstract

The tiger mosquito is a key vector of several human diseases and is considered a public health concern worldwide. The implementation of strategies aimed at maximizing mosquito control without affecting non-target insect groups is of major importance. In a field trial, we tested the efficiency of a natural pyrethrum-based vs. a synthetic pyrethroid-based insecticide in reducing tiger mosquito population and how they affect the diversity of non-target flower-visiting insects in green urban areas. Only the pyrethroid insecticide was effective in reducing mosquito abundance, although its effects disappeared nine days after application. The two adulticides did not significantly affect the diversity of flower-visiting insects, probably because of their large body size and the difference in flying and foraging activity. To effectively control mosquito populations while preventing intoxication of non-target flower-visiting insects, adulticide applications should be applied early in the morning and only on bushes and trees. Results from our small-scale applications cannot be extrapolate when larger areas are treated.     

法氏囊活性肽在大肠杆菌中的克隆与表达

法氏囊活性肽（Bursin,BS)作为一种免疫增强剂，临床应用广泛，为了大量制备BS，按大肠杆菌惯用密码子合成BS基因。并用色氨酸将5个BS基因串联，克隆于质粒pU57的SmaI位点，经测序证明序列正确后，以PCR扩增，克隆于表达载体pBV220的EcoRI,HinDⅢ位点，温敏诱导表达，其表达水平占全菌总蛋白的13.4%。