南方早熟砂梨缺镁黄叶症诊断与矫治

通过对福建省德化县早熟砂梨“黄叶病株”及“正常植株”叶片及土壤的营养诊断分析：黄叶病株叶片平均含镁量0.131%,极显著低于正常植株0.328%;黄叶症较重的果园土壤交换态镁含量低12.6～24.5㎎/㎏及土壤酸性强pH3.6～4.5,诊断结论砂梨叶片黄化现象为镁素缺乏所致。矫治试验效果,叶面喷施1%硝酸镁3次,可以叶色转绿;12月份土壤基施钙镁磷肥株1.3 kg,翌年5月份后有明显矫治效果。     

基于主动冠层光谱仪的莴苣生物量及氮素营养状况估测

[目的]研究冠层光谱技术在蔬菜氮素营养诊断中应用的可行性和提高其准确性的方法,为推进蔬菜氮素营养管理与施肥推荐提供快速无损检测技术.[方法]以茎菜类蔬菜—莴苣(Lactuca sativa L.)为研究对象进行田间试验.设置5个化肥年施用梯度:0、108、162、216、270kg/hm2,在莴苣幼苗期、莲座期、茎形成...     

玉米果穗不同部位子粒水分动态差异研究

为明确玉米果穗不同部位子粒含水率和脱水速率的动态变化差异,在春玉米区宁夏银川和夏玉米区河南新乡采用8个不同熟期和脱水速率的品种,将玉米果穗垂直等分为5个部位,定期测定不同部位子粒含水率,计算子粒脱水速率。结果表明,玉米生长中后期,果穗上部子粒含水率低于中下部子粒含水率,生理成熟前各部位子粒含水率的差值低于生理成熟后。参试品种生理成熟前20 d时不同部位子粒含水率极差低于3%,成熟期的极差值变幅为0.6%～5.2%,生理成熟后极差最大值可达6.2%。同一果穗自上而下子粒的脱水速率逐渐降低,品种之间有明显差异,先玉335、迪卡517和迪卡519果穗不同部位子粒脱水速率差异较大。果穗中部子粒脱水速率和平均脱水速率与不同部位子粒含水率的极差值呈负相关。     

一例猪圆环病毒病继发链球菌的诊治

猪感染圆环病毒后,因免疫系统遭到破坏而容易继发其他疾病,如果猪圆环病毒病继发感染链球菌,对养猪业危害巨大。2019年4月年对辽宁地区某规模化猪场发生的疫情进行了实验室诊断,并根据检测结果提出了治疗方案,疫情得到控制。     

基于Lucid多途径检索的油茶害虫诊断APP开发与实现

油茶是亚热带地区重要的木本油料作物,近年来随着种植面积的不断扩大和集约化经营,病虫害问题日益严重,对油茶的产量和品质造成不同程度的影响。本研究通过野外调查、文献查阅、种类鉴定等工作,整理了21种油茶主要害虫的形态特征、生物学习性、为害特点、防治措施等信息,并拍摄相应害虫及为害状的高清照片1 600张。采用Lucid智能诊断系统,构建Fact Sheet Fusion基础信息数据库,并针对多途径检索方式提取害虫"为害方式"、"为害部位"、"为害高峰期"、"形态特征"等4个1级特征组,以及10个2级特征和18个3级特征,共组成102个特征状态,构建了油茶害虫的快速诊断系统。在此基础上,转换得到基于Android系统的手机应用APP,为林农和森防一线工作者对油茶害虫快速识别和防治提供便捷服务,从而促进油茶产业持续健康发展。     

一起羊传染性脓疱的诊治

秦州区汪川镇刘斜村,属贫困村,养殖户共计18户,其中养猪户10户,养鸡户2户,养牛户4户,养羊户2户,总计饲养量达11300余头只,属养殖大村。两户养羊户共计饲养羊82只,发病17只,发病率20.7%。给养殖户造成了重大的经济损失。本文根据发病情况、病因调查、临床检查、综合诊断,提出有效的防治措施,从治疗效果上取得了显著的成效,治愈率100%,为养殖户最大程度地降低了经济损失。获得了良好的社会效益。     

基于ResNet-50深度卷积网络的果树病害智能诊断模型研究

[目的/意义]果树病害危及农业生产安全,运用人工智能技术帮助果农及时准确地识别果树病害对保障农业安全生产具有重要意义.[方法/过程]采用10 000张果树叶片病斑图像数据集,通过旋转、污化、增噪、切割等图像增强手段,提高样本图像的多样性;使用ResNet-50深度卷积网络模型,进行机器学习,获得果树病害识别模型,并基于...     

牛日本血吸虫病5种血清学诊断技术比较

为找寻特异性强、敏感性高,且操作简便、费用低廉,并能大规模应用于临床的日本血吸虫病血清学诊断方法,以疫区黄牛为研究对象,应用环卵沉淀试验(COPT)、血清法间接血凝试验(sIHA)和血纸法间接血凝试验(bpIHA)、胶乳凝集试验(PAPS)、三联斑点酶联免疫吸附试验(三联Dot-ELISA)5种血清学诊断方法与粪检方法检测牛日本血吸虫病,并对5种血清学检测结果进行评价.检测分析结果表明,用血清学方法COPT,sIHA,三联Dot-ELISA对疫区黄牛进行血吸虫病检测,与三粪九检结果符合率高,具有灵敏度高、特异性好、简捷方便、费用低等特点,特别适用于疫区家畜血吸虫病的诊断、普查,是比较理想的现场检测方法,值得推广.血清学方法bpIHA和PAPS检测血吸虫病,尽管方法简便、费用低廉,但其灵敏度、特异性与三粪九检结果符合率低于血清学方法COPT,sIHA,三联Dot-ELISA,易造成漏检,假阳性,故在普查时,不建议采用.     

Cloning and expression of a surface immunogenic protein in Streptococcus dysgalactiae isolated from fish and its application in enzyme‐linked immunosorbent assays to diagnose S. dysgalactiae infections in fish

Lancefield group C Streptococcus dysgalactiae (GCSD) causes severe necrotic lesions in the caudal peduncle in the genus Seriola farmed in Japan. To develop a sero‐diagnostic method for GCSD infection in farmed fish, we attempted to identify a surface immunogenic protein that induces an antibody after infection with GCSD by immunoblot analysis using sera collected from infected fish. A protein obtained from sodium dodecyl sulfate (SDS) extracts of GCSD was identified as S. dysgalactiae surface immunogenic protein (Sd‐Sip). Sd‐Sip exhibited more than 94% homology with a surface antigen or a hypothetical protein from S. dysgalactiae mammalian isolates at the nucleotide sequence level. Expression of the recombinant Sd‐Sip (rSd‐Sip) was confirmed by immunoblot analysis, that is, its reactivity to GCSD‐infected sera. Antibody detection ELISA using rSd‐Sip and their usefulness for diagnosis of GCSD infection were examined. GCSD‐infected sera collected from farmed amberjack, Seriola dumerili (Risso), showed strong reaction with immobilized rSd‐Sip. Meanwhile, sera immunized by other pathogenic bacteria of fish were showed ELISA values similar to those of non‐infected sera. These results of this study suggest that the antibody detection ELISA using rSd‐Sip is an effective diagnostic method for GCSD infection in fish.     

Quantification of Flavobacterium psychrophilum in rainbow trout, Oncorhynchus mykiss (Walbaum), tissues by qPCR

A qPCR assay was developed for rapid and sensitive detection of Flavobacterium psychrophilum, the aetiological agent of bacterial cold-water disease and rainbow trout fry syndrome in salmonid fish worldwide. A set of F. psychrophilum-specific primers based on 16S rRNA gene sequences was designed and validated for specific detection and quantification of DNA isolated from representative strains of F. psychrophilum. The qPCR assay exhibited a high specificity for the 16S rRNA gene of F. psychrophilum (from 4 × 10(8) down to 11 copies per reaction) but not for other Flavobacterium species or other bacteria including fish pathogens. This qPCR-based method proved to be useful in the quantification of the F. psychrophilum titre present within organs dissected out from diseased fish. As the F. psychrophilum genome contains six copies of the 16S rRNA gene, we could infer a limit of detection corresponding to two bacteria per reaction, corresponding to 800 bacteria per fish tissue sample, and therefore 20 F. psychrophilum cells mg(-1) of tissue (for sample weighing 40 mg). The qPCR assay reported here could be a useful tool for veterinary diagnostic laboratories to monitor the F. psychrophilum infection level in fish farms.