中国大陆沿海六水系绒螯蟹(中华绒螯蟹和日本绒螯蟹)群体亲缘关系:RAPD指纹标记

用 4 8个具有丰富多态性的 10碱基随机引物对辽河、黄河、长江、瓯江、珠江和南流江的中华绒螯蟹和日本绒螯蟹的 6个群体进行RAPD分析。结果发现 :(1)两个引物具有群体特异性带 ,其中Z2扩增的 880bp片段为珠江蟹和南流江蟹群体中所特有 ,而 70 0bp片段为长江蟹、辽河蟹、黄河蟹和瓯江蟹所特有 ,可作为区别日本绒螯蟹和中华绒螯蟹的分子遗传标记 ;(2 )Opp17扩增的 94 7bp片段的出现频率 ,在长江、黄河和辽河群体显著地从南到北递减 ,长江蟹 87.50 %、黄河蟹4 1.66%、辽河蟹 10 .83%。这一遗传渐变的度量可作为区别这三个水系的中华绒螯蟹种群的判据 ;(3) 6水系群体内的平均遗传相似度依次为 :辽河蟹 0 .90 8>南流江蟹 0 .897>瓯江蟹和珠江蟹 0 .895>黄河蟹 0 .890 >长江蟹 0 .850 ;6群体间遗传距离及其UPGMA、NJ聚类分析进一步表明 ,南流江蟹、珠江蟹同长江蟹、辽河蟹及黄河蟹在基因组之间存在明显的歧化。     

莫莫格湿地干-湿界面优势植物种群动态分析

莫莫格湿地从高河漫滩底端到顶端选取有代表性的植物群落片断作为固定观测样带,并设置6个观测样方,生长季5月、7月、9月3次观测结果表明,小叶章优势种群5月份密度最高达1154-1594株/平方米,7月种群数量下降,9月有所升高;踏头苔草优势种群5-7月份密度在3 414-7 193株/平方米,9月份种群数量大幅度下降;土壤相对含水量低地段小叶章种群相对优势度大,土壤相对含水量高地段踏头苔草种群相对优势度大,局部地段生长季内有相对优势度相互替代过程,莫莫格湿地干-湿界面上小叶章和踏头苔草两个种群可以共存。     

西花蓟马孤雌产雄生殖繁育的后代种群生命表的建立

孤雌生殖是西花蓟马(Frankliniella occidentalis)繁殖的一种重要方式。前期研究发现,西花蓟马在高温下,雌性的存活率远大于雄性。为探究高温处理后仅有雌性西花蓟马孤雌产雄的情况下其后代建立种群的可能性,试验设定:高温(45℃,2 h)处理西花蓟马单个雌性个体,分别进行孤雌产雄生殖后,雄性子代(F1代)与其母系回交产生F2代;高温(45℃,2 h)处理西花蓟马多个雌性个体,进行孤雌产雄生殖后,雄性子代(F1代)与亲代多个雌性个体共存情况下进行交配产生F2代。两组处理模式下建立F2代实验种群生命表。结果表明,上述两种处理模式,母代雌性个体与子代雄性个体交配后均可产生后代,雄性F1代与其母系回交产生的F2代的雌雄性比为1.05∶1;与亲代多个雌性个体共存下交配产生的F2代性比为1.55∶1。雄性F1代与其母系回交产生的F2代的平均单雌产卵量(F)和内禀增长率(rm)显著小于与亲代多个雌性个体共存下交配产生的F2代(P0.05);各龄期的平均发育历期、平均产卵前期和平均总产卵前期2个繁殖力参数以及净生殖率(R0)、平均世代周期(T)2个种群参数,前者则比后者长(P0.05);另周限增长率(λ)两者之间无显著差异。研究表明西花蓟马在孤雌产雄状态下仍然可以在短期建立种群,具有较强的抗高温能力和繁殖能力,为其成功入侵奠定了生态学基础。     

苹果桃小食心虫发生规律研究

为掌握桃小食心虫的活动规律、有效测报及防治提供理论依据,采用性诱剂诱集的研究方法,研究苹果桃小食心虫的发生规律。结果表明：苹果桃小食心虫1 年发生2~3 代,成虫发生量最高峰发生在7 月20 日,有世代重叠现象;桃小食心虫成虫在苹果树上1.0~2.0 m处的分布无显著差异,在运用性诱剂诱杀桃小食心虫成虫时,可根据操作方便的原则,在苹果树1.0~2.0 m处随意设置性诱剂,不会影响诱集效果;成虫主要在22:00 以后,至清晨6:00 时间段活动,其中在0:00—2:00 时间段活动最频繁、最活跃。试验更进一步了解了桃小食心虫的发生规律,为更有效地防治提供参考。     

石河子垦区奶牛临床型乳房炎的发病规律及治疗现状

为了统计和研究石河子垦区大中型奶牛场临床型乳房炎的发病规律及治疗情况,选择石河子垦区6个大中型奶牛场2 600头奶牛作为调查对象,通过对临床型乳房炎进行鉴定及不同治疗方法进行比较。结果表明2 600头奶牛在4—9月份临床型乳房炎发病270头,发病率10.38%;10—3月份发病163头,发病率6.99%。目前在石河子垦区大中型牛场一般常见的治疗药物主要有左旋咪唑拌料、青霉素钾或先锋Ⅴ等＋糖皮质激素、中草药组方和青霉素钾或先锋Ⅴ等＋中草药组方等。结果,经过预防和治疗后,在4—9月份奶牛临床型乳房炎发病率降至4.92%;10—3月份奶牛临床型乳房炎发病率降至3.00%。调查结果表明：中西医结合用药对临床型乳房炎起到了积极的治疗作用。     

Detection of calves persistently infected with bovine pestivirus in a sample of dairy calves in south-eastern Queensland

Objective To determine the proportion and incidence of calves persistently infected with bovine pestivirus in calves (n = 1521) supplied to the Tick Fever Research Centre and to assess the test regime to detect calves persistently infected with bovine pestivirus.
Design Calves, 1 to 6 weeks old, selected for use in the production of the tick fever vaccine were collected from 21 properties in 56 separate groups between October 1990 and December 1996. Each group was examined for the presence of calves persistently infected with bovine pestivirus.
Procedure All calves were routinely tested for antibody to bovine pestivirus and bovine pestivirus antigen using a serum neutralisation test and an antigen-capture ELISA, respectively. Pooled lymphocyte samples from calves were also monitored for bovine pestivirus by inoculation of sheep. Whole herd testing was carried out in eight herds, using a serum neutralisation test as a screen test followed by an antigen-capture ELISA of cattle with a serum neutralisation test titre of less than 32.
Results Fourteen of the 1521 calves tested (0.9%), were detected as persistently infected and the incidence ranged from 0.0 to 3.0 % per year over 6 years. Persistently infected calves were found in 13 of the 59 groups and originated from 7 of the 21 herds used. In whole herd testing on the properties of origin, cattle persistently infected with bovine pestivirus were detected in four of the eight herds tested
Conclusions The proportion of calves persistently infected with bovine pestivirus is similar to that in other countries and indicates that bovine pestivirus could be a significant cause of economic loss in Australian cattle herds. In detecting calves persistently infected with bovine pestivirus, the combination of sheep inoculation, paired antigen-capture ELISA and serum neutralisation tests appeared to be highly sensitive and specific.     

AFLP fingerprinting of Anchusa (Boraginaceae) in the Corso-Sardinian system: Genetic diversity, population differentiation and conservation priorities in an insular endemic group threatened with extinction

Although several plants endemic to Corsica and Sardinia are included in various redlists, no attempts have been made to analyse their genetic diversity with molecular techniques. Genus Anchusa occurs with seven taxa in either mountain or coastal habitats of the two islands, but the very restricted range and low population size pose these endemisms in a very precarious conservation status. Highly variable markers (AFLP) were therefore used to analyse the patterns and levels of genetic diversity in a sample of 11 populations from the entire range of the group.Results indicate the separation between a mountain genic pool including Anchusa formosa, Anchusa capellii and Anchusa montelinasana, and four groups of coastal accessions. In spite of small size, mountain taxa show low interpopulation differentiation (F_st = 0.02) and relatively high intrapopulation genetic variation (0.365), while coastal accessions showed on average a stronger differentiation (mean F_st = 0.20) and a lower diversity (0.281), possibly due to higher rates of inbreeding. The particularly low levels of variation found in A. sardoa, A. littorea and A. crispa ssp. maritima from the Coghinas bay are likely due to a historical decrease of populations and to bottleneck events caused by loss of habitat and natural stochastic factors on sand dune ecosystems. While habitat maintenance and regulation of grazing by domestic herbivores should be sufficient to ensure the persistence of the mountain endemics, additional actions of in situ and ex situ conservation are needed for the critically endangered coastal species A. sardoa and A. littorea. A. crispa showed a relatively high variation, especially on Corsica. No correlation between population size and genetic variation was found in the latter species, highlighting the importance of the small patches for its conservation. Also, the genetic separation between subspecies crispa and maritima stresses the need of keeping them distinct in redlists and conservation actions on Sardinia.     

基于SSR标记的苜蓿种质资源遗传多样性与群体结构分析

种质资源遗传多样性和群体结构的分析是进行复杂性状关联分析的前提条件.从140对SSR引物中筛选到16对多态性引物,对82份苜蓿(Medicago spp.)材料进行遗传多样性与群体结构分析.结果表明;16对SSR引物共检测出190个等位变异,平均11.88个;多态性比率66.67％～100％,平均为83.05％;基因多样性为0.1447～0.3637,平均为0.2577;PIC为0.0079～0.9432,平均为0.5501.群体结构分析表明,当K=5时△K最大,即82份苜蓿材料可划分为5个类群,其中75.61％的种质遗传组分相对比较单一,24.39％的种质遗传背景比较复杂.苜蓿种质资源遗传多样性丰富,群体结构的划分与种质的来源不完全相关.     

籼稻栽培品种中淀粉合成相关基因的遗传变异和群体结构分析

选用34个淀粉合成相关基因分子标记对87份来自不同国家和地区的籼稻栽培品种进行遗传变异和群体结构分析.结果表明,34对引物共检测到80个等位变异,平均每个位点含2.35个等位基因,品种间等位基因变异范围2～6;Shannon's信息指数变幅为0.303 ～0.796,平均为0.539;多态信息含量(PIC)的变幅为0.084～0.658,平均0.295;遗传相似系数变幅为0.265 ～0.990,表明淀粉合成相关基因在品种间存在遗传差异,但不同品种间等位基因的变异频率不同.87份籼稻品种可以分成3个类群,类群内品种遗传背景比较相似,类群间品种遗传背景差异明显,其中,39.1％的籼稻品种遗传组分单一,而遗传背景复杂的籼稻品种达到60.9％.该研究可为水稻淀粉品质的遗传改良提供依据,并为后续淀粉品质性状的关联分析奠定基础.     

不同栽培方式对水稻纹枯病控制效果试验

分别在水稻分蘖盛期、孕穗末期—黄熟期进行点播、撒播、强化栽培、插植、抛秧等5种栽培方式下稻田纹枯病病害情况调查。结果表明,点播、撒播稻田纹枯病发生程度较轻;抛秧稻田发病程度与插秧稻田相当;强化栽培稻田纹枯病发病率和病情指数比其他栽培方式的高。因此,强化栽培方式种植水稻更要做好纹枯病的预防工作,做到适时用药,合理安排种植密度,以达到控制该病害的目的。