灌区灌溉自动化监控系统的设计与研究

介绍了 1种灌区灌溉自动化监控系统的组成、功能和实现方法。系统利用田间传感器实时测量田间参数 ,通过网络传送给控制计算机 ,由控制计算机根据决策模型自动控泵房电机起停、渠首闸门启闭实现灌区内农田自动灌溉 ,系统具有实时控制、实时数据采集与保存 ,现场实时视频监视等功能。     

“数字清江”实时水情调度联合计

为了快速、准确的分析水情实况、预测未来的发展趋势，结合清江流域防洪减灾工作实际情况，设计了实时水情调度联合计算方案。根据清江流域地理位置的特点，将其分为7个子流域，依次进行降雨径流预报、洪水演算，为防洪减灾提供真实有效的决策依据。通过对该方案的分析，探讨了设计思路，并给出了其实现机理。该方案已在“数字清江”项目中得到成功应用。     

Determination of vc and mating types of Cryphonectria parasitica isolates by multiplex PCR and their genetic diversity in 13 chestnut-growing provinces of Turkey

Vegetative compatibility (vc) and mating types and genetic diversity of Cryphonectria parasitica isolates were determined using 183 isolates obtained from 215 infected chestnut trees growing in 13 provinces of Turkey. Based on the cultural aspects, 143 of these isolates were evaluated as virulent whereas the remaining 40 isolates were hypovirulent. When vc types of 183 isolates were classically differentiated, 135 of them matched to EU-1 (82.3%), 29 of them to EU-12 (17.6%) vc type, whereas 19 of them did not match to the two. When molecular vic markers were used, all the isolates were assigned to two EU vc types; 149 to EU-1 (81.4%) and 34 (18.5%) to EU-12. Of the majority of the isolates, 134 (73.2%) had mating-type MAT-1, while 44 (24%) isolates had MAT-2 and 5 (2.8%) isolates had both mating types. The population analysis based on two DNA marker systems, Inter-Primer Binding Site and Start Codon Targeted Polymorphism, showed no intraspecific genetic variation among the C. parasitica isolates. The prevalence of two dominant vc types revealed by this study shows that biological control with hypovirulent EU-1 and EU-12 isolates will be significant for the country. The results might be helpful to chestnut breeders carrying out resistance breeding studies to manage this disease based on hypovirulence attributed to Cryphonectria hypovirus 1.     

茶树咖啡因合成酶基因RNA干涉表达载体构建

咖啡因合成酶（TCS）是茶树咖啡因生物合成途径中的一个关键酶,催化7-甲基黄嘌呤转变为可可碱和可可碱转变为咖啡因。抑制TCS基因表达是培育低咖啡因茶树的最有效途径。用RT-PCR方法扩增茶树TCS基因的两个cDNA片段,并克隆入T-载体中。干涉载体和TCS基因片段的T克隆经限制性内切酶两次双酶切与连接,将两个TCS基因片段分别反向重复插入到干涉载体pFGC5941,构建了TCS基因的RNA干涉载体,分别命名为pFGC5941-TCS02和pFGC5941-TCS03。经PCR和DNA测序获得验证。TCS基因RNA干涉载体的构建为培育低咖啡因茶树奠定了基础。     

A serological and molecular study on Francisella tularensis in rodents from Hamadan province,Western Iran

Introduction and purposeTularemia is a zoonotic disease, the most important hosts of which are rodents. Endemic regions and reservoirs of F. tularensis are not well-researched areas in Iran. The present study aimed to study F. tularensis infection in the rodent populations of western Iran.Materials and methodsSamples were collected in different areas of Kabudar Ahang County in Hamadan province (west of Iran) from 2014 to 2017. Tularemia serological and molecular tests were conducted using the tube agglutination test and Real-time PCR method tracking the ISFtu2 gene. Positive serum samples were evaluated for cross-reactivity with brucellosis.ResultsA total of 433 rodents, collected from 33 localities, were included in the study. The most abundant species belonged to the Persian jird (Meriones persicus; 75.5%), and Libyan jird (Meriones libycus; 10.1%). Among the studied samples, three (0.74 %) were seropositive and five (1.15%) were PCR positive. Seropositive samples were two M. persicus and one M. libycus, and PCR positive rodents were four M. persicus and one M. vinogradovi. Tularemia seropositive samples showed no cross-reactivity with brucellosis.ConclusionGiven the presence of infection in rodents with tularemia agent in the studied area, it is crucial to elucidate the risks of rodent exposure to tularemia for physicians, health personnel and the general population.     

柑橘黄龙病菌浓度对琼中绿橙果实品质的影响

为了定量衡量黄龙病菌量对琼中绿橙果实品质的影响,本实验以采自海南琼中橘园中感染了柑橘黄龙病的琼中绿橙为实验材料,用实时荧光定量PCR相对定量的方法测定果实中柑橘黄龙病菌的浓度,同时对果实品质的8个外在指标（果实纵经、横径、果形指数、单果重、果皮率、残渣率、种子数量、种子重量）和5个内在指标（果汁率、可食率、可溶性固形物含量、可滴定酸含量、固酸比）进行测定,研究黄龙病菌浓度对琼中绿橙果实品质的影响。结果表明：随着琼中绿橙果实中柑橘黄龙病菌浓度的增大,果实外观品质变化明显的指标包括果实纵经、果形指数、单果重（p<0.05）,其中果实纵经呈现明显下降趋势,从64.97mm下降到57.44mm,相对较少11.59%;果形指数呈现明显上升趋势,从0.83上升到0.94,相对增多13.25%;单果重呈现下降趋势,从166.35g下降到109.66g,相对较少34.08%;果实横径、果皮率、残渣率、种子数量、种子重量等指标变化不明显。随着琼中绿橙果实中柑橘黄龙病菌浓度的增大,果实内在品质变化明显的指标为可溶性固形物含量,可溶性固形物含量呈现明显下降趋势（P<0.05）,从9.65%下降到8.19%,相对减少15.13%;果汁率、可食率、可滴定酸含量和TSS/TA没有明显变化。结论：在黄龙病菌浓度增加的情况下,琼中绿橙在果实外观、内在品质等多个指标呈现下降趋势。研究结果为定量评价黄龙病对柑橘果实的影响提供参考。     

3种含氯消毒剂对柑橘黄龙病菌室内防治效果研究

柑橘黄龙病是柑橘生产上最具毁灭性的病害,目前没有防治特效药也没有较好的抗性品种。本文以含氯消毒剂作为柑橘黄龙病菌防治的候选药剂开展药剂筛选试验。将染病接穗分别浸泡3种含氯消毒剂再嫁接到健康枳壳砧木上,利用定量PCR技术定量分析药剂处理前后黄龙病菌含量的变化,建立柑橘黄龙病菌药剂防治效果评价体系。试验结果表明,漂白粉（CH）不适合利用嫁接技术进行候选药剂筛选;二氯异氰尿酸钠（NaDCC）和三氯泡腾消毒片（TCCA）的抑菌效果随处理浓度的降低而减弱,在有效氯含量为5000mg/L时,病菌减退率最高,分别为99.1%和99.5%,相对防效最佳,分别达到了97.9%和98.8%,与对照药剂盐酸四环素(TET)的抑制效果相当,说明NaDCC和TCCA可以作为柑橘黄龙病化学防治的候选药剂。     

猪圆环病毒的研究进展

猪圆环病毒（PCV）分为两个血清型PCV1和PCV2。目前认为PCV2是断奶仔猪多系统衰弱综合征（PMWS）的主要病因,另外,还与猪的多种疾病有关,PCV已经成为目前危害养猪业的主要病毒之一。本文对PCV的特性、流行特征、致病机理、诊断方法以及防治措施作了较全面的综述。     

Rapid screening of genetically modified ingredients in soybean and cotton processing by-product and waste using direct qPCR

To develop a simple and fast method for screening genetically modified ingredients from processing by-product and waste, direct quantitative PCR (qPCR) kit-Taqman which omitting multi genomic DNA preparing steps was developed in this study. A total of 18 oil crop processing by-products and wastes including 10 soybean and 8 cotton materials were collected from food processing factories. Compared with 2 commercial direct qPCR kits, conditions of DNA releasing procedure and PCR amplification were optimized. Element screening was performed at the initial step of genetically modified (GM) ingredient testing procedure via direct qPCR. GM event identification was carried out in positive samples by initial screening. Totally 5 screening elements (P–35S, T-NOS, Cp4-epsps, bar and pat) for soybean materials and 6 screening elements (P–35S, T-NOS, NPTII, Cry1Ac, bar and pat) for cotton samples were detected. In GM event identification, MON531 and MON1445 were found in cotton materials. Results were further confirmed by real-time PCR with DNA extraction and purification. The direct qPCR system proposed by this research was convenient for rapid screening and identification of GM ingredients in oil crop primary by-product and waste.