槭叶苹婆60Co-γ射线辐射诱变初报

用60Co-γ射线辐射槭叶苹婆种子,并对种子的萌发和幼苗生长进行观察.结果表明:辐射对槭叶苹婆的种子萌发、成苗率、幼苗高生长、叶面积存在影响.3 kR的辐射剂量对种子萌发有一定的促进作用,大于3 kR的高剂量则有抑制作用;辐射降低幼苗成苗率;辐射抑制苗高生长和叶片生长,但过高剂量叶片会增大并扭曲;初步认定槭叶苹婆种子辐射的半致死剂量为4 kR,适宜辐射剂量为3.0～4.5 kR.     

新型鸭呼肠孤病毒RT-PCR检测方法建立与初步应用

为建立一种能够快速检测新型鸭呼肠孤病毒（NDRV）的方法,本研究参考GenBank上登录的NDRV S3基因保守序列设计特异性引物.经条件优化后,建立了检测NDRV的RT-PCR方法.对其特异性、敏感性和重复性进行检验.结果显示：该方法仅能从NDRV分离毒中扩增到与预期大小相符,长度为298 bp的特异性目的片段,检测灵敏度达到83.4 pg病毒RNA;而其它病毒：番鸭呼肠孤病毒、禽呼肠孤病毒、鸭病毒性肝炎病毒、鸭瘟病毒、鸭新城疫病毒和禽流感病毒等样品的扩增结果均为阴性.采用该方法对在广东不同地区采集的15份鸭病料样品进行检测,NDRV阳性率为53.33％.表明建立的RT-PCR方法特异性强、敏感度高,可用于NDRV的临床诊断和流行病学调查.     

猪伪狂犬病抗体免疫金标快速检测试纸法

应用免疫学原理与胶体金层析技术相结合，采用双抗原夹心法建立了检测猪伪狂犬病抗体水平的“猪伪狂犬病抗体免疫胶体金快速检测试纸法”，用该法与美国Idexx公司的猪伪狂犬病ELISA试剂盒，同时对16纷猪血液或血清进行抗体水平检测，符合率达100％。同时使用金标法对100份猪血液和对应血清进行检测，结果也相同。试验结果显示．金标法与ELISA一样，具有微量、特异、准确等优点，且操作简易，而金标法不需要任何仪器，检测时间短．结果直观，容易判定，适用于基层兽医站、养猪场使用和大面积猪伪狂犬病抗体普查。     

一例鸭鼠伤寒沙门氏菌的分离鉴定及抗原性分析

对出现精神沉郁、食欲减退、拉稀、脚软和共济失调症状,其后死亡,的鸭病例,进行常规诊断、动物试验,结果分离到一株细菌,命名为GDYJS-1.分离株通过生长特性、凝集试验、染色特性及VITEK-32微生物鉴定系统生化试验鉴定为沙门氏菌;16S rRNA基因序列的测定与分析,鉴定为鼠伤寒沙门氏菌.     

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.     

基于BTO多目标遗传算法的播种机性能优化设计

受播种地形和地域的影响,大部分播种机的播种质量、播种效率和能耗不能发挥到最佳状态,为了提高播种机的作业性能,深入挖掘了按顾客订单生产(Build-to-Order,BTO)模式的一般性意义,并将该模式引入到了播种机的优化设计中,提出了一种基于BTO模式的多目标速度控制遗传算法优化模型。根据播种质量、效率和能耗的要求,首先确定了BTO模式下播种机性能优化的初始参数,利用多目标函数确定了播种机的速度控制模型,并利用遗传算法进行了优化设计。最后,通过试验样机对播种机的播种性能进行了测试,结果表明:使用多目标遗传算法对播种机的性能进行优化后,播种机的播种质量、播种效率和播种能耗有了明显的改善,为新型播种机的研发提供了较有价值的参考。     

籽瓜收获机械研究现状与发展展望

籽瓜是我国北部地区重要的经济作物之一,研发适合我国农业现状的籽瓜收获机械,对降低劳动强度、提高籽瓜收获效率及我国农民的经济实力具有重要的意义。为此,分析了国内外籽瓜收获机械的研究现状,结合我国籽瓜种植模式,探讨现有籽瓜收获机械存在的问题,同时指出了籽瓜收获机向大型化、专业化和智能化收获发展的趋势,为提高籽瓜收获机械化水平提供了一定的参考依据。     

柠檬酸对茶园紫色土微团聚体竞争吸附Zn、Cd影响

采用批量培养和平衡吸附法,选取原土及微团聚体颗粒组为对象,研究Zn(II)、Cd(II)单一存在、二元竞争及竞争体系中加入柠檬酸(0.1,1,10mmol/L)等3种处理的等温吸附特性及影响。结果表明:(1)以专性吸附方式为主的多层吸附随Zn~(2+)、Cd~(2+)强度增加逐渐饱和,吸附能力以0.002mm最优、0.05~0.002mm和原土次之,0.25~0.05mm和2~0.25mm结合能力稍差,不同条件下Cd较Zn更易积累。吸附过程为自发吸热反应,热力学Freundlich方程(Zn:R2=0.960~0.997;Cd:R2=0.957~0.995)拟合结果优于Langmiur方程(Zn:R2=0.952~0.995;Cd:R2=0.913~0.991)。最大吸附量与有机质含量具有显著相关性。(2)单一处理Zn、Cd的固持效果明显、共存处理时Zn、Cd竞争行为表现为彼此削弱,Zn对Cd的吸附具有更强抑制作用。(3)添加不同浓度柠檬酸后Zn、Cd吸附水平介于单一及共存处理之间呈动态变化(Zn、Cd接近),0.1~1mmol/L利于Zn、Cd固持,增至10mmol/L后加速淋洗,仅0.002mm粒径富集量持续提升。表明柠檬酸作为一种调节剂,能适度保持土壤Zn供给并弱化Cd迁移活性,缓解茶园土壤复合污染。     

枯草芽孢杆菌抗菌物质对镰刀菌抑制机理的镜下研究

 将枯草芽孢杆菌B-903菌株液体培养72h后,将培养滤液高温灭菌,以不同比例将培养滤液加入镰刀菌孢子悬浮液中,置于扫描电镜和光学显微镜下定时观察。在处理12h后,镰刀菌孢子芽管顶端、菌丝末端及菌丝中央的多处细胞均可发生畸形的球状结构,这种畸变结构随处理时间延长而增加,致使菌丝变成捻珠状。处理36h后,畸变球形细胞及菌丝纷纷断裂离解,细胞内含物渗出,致使大部分细胞成为空泡。到处理48h后,镜下几乎无完整菌丝,均成单个的球状细胞空泡,这些空泡最终胞壁崩裂,不复存在。笔者认为正是枯草芽孢杆菌在生活过程中分泌到体外的抗高温代谢物对镰刀菌孢子和菌丝细胞的这种畸变作用造成拖子和菌丝失活,侵染能力丧失。     

Rapid detection of Phytophthora cinnamomi using PCR with primers derived from the Lpv putative storage protein genes

Phytophthora cinnamomi is an ecologically and economically important pathogen. In this study, PCR assays were developed with primer pair LPV2 or LPV3 for rapid detection and identification of this organism. Both primer pairs were selected from putative storage protein genes. The specificity of these primer pairs was evaluated against 49 isolates of P. cinnamomi , 102 isolates from 30 other Phytophthora spp., 17 isolates from nine Pythium spp. and 43 isolates of other water moulds, bacteria and true fungi. PCR with both primer pairs amplified the DNA from all isolates of P. cinnamomi regardless of origin. The LPV3 primers showed adequate specificity among all other species tested. The LPV2 primers cross-reacted with some species of Pythium and true fungi, but not with any other Phytophthora species. PCR with the LPV3 primers detected the pathogen at levels of a single chlamydospore or 10 zoospores in repeated tests. The PCR assay was at least 10 times more sensitive than the plating method for detection of the pathogen from artificially infested soilless medium, and, to a lesser extent, from naturally infected plants. PCR with LPV3 primers can be a useful tool for detecting P. cinnamomi from soilless media and plant tissues at ornamental nurseries, whereas the LPV2 primers can be an effective alternative for identification of this species from pure culture. Applications of these assays for detection of P. cinnamomi in other environments were also discussed.