四倍体杂交冰草SRAP和SSR分子标记遗传连锁图谱构建

为了给后期冰草抗旱耐寒基因筛选及QTL图位克隆搭建平台,并为产量及相关性状QTL定位和分子标记辅助育种奠定基础,以航道冰草和蒙古冰草为亲本,杂交加倍后随机选取180个F₂分离单株为作图群体,利用SRAP和SSR分子标记进行四倍体杂交冰草遗传连锁图谱的构建。结果表明,构建的图谱包含475个标记（240个SRAP标记和235个SSR标记）,分布于14个连锁群,图谱全长为1 592.7 cM,标记间平均间距为3.35 cM,各连锁群长度范围为67.6~145.2 cM。该图谱密度较高、标记位点分布均匀且连锁群更加饱满。     

水流和光照条件对舌状蜈蚣藻Grateloupia livida (Harv)Yamad果孢子萌发生长的影响

在不同水流和不同光照条件下,分别对舌状蜈蚣藻Grateloupia livida (Harv)Yamad果孢子萌发情况展开研究,以期为其苗种生产奠定基础。舌状蜈蚣藻果孢子在附着1 d、15 d后,置于不同水流速度(0、1、1.5、4、7、10、14 cm/s;1.5 cm/s流速由充气控制,其他流速由流水装置控制)培养20 d;舌状蜈蚣藻果孢子附着1 d后,在不同光照周期(6L∶18D、8L∶16D、10L∶14D、12L∶12D、14L∶10D、16L∶8D)和不同光照强度(35、85、135 µmol photons/m2·s)交叉条件下培养70 d。结果显示,附着1 d的果孢子萌发体在静止条件下的萌发生长明显优于其他水流速度下的(P<0.05);附着15 d的果孢子萌发体在1.5 cm/s流速下的萌发生长最好(P<0.05),在静止条件下的萌发生长明显慢于其他流速下的各组(P<0.05)。光照周期和光照强度对果孢子萌发生长的影响显著(P<0.05),这二者对盘状体和孢苗生长的影响具有交互作用(P<0.05),对盘状体萌发出直立体的影响没有交互作用(P>0.05)。光照时间为8–10 h,盘状体萌发直立体的百分率以及孢苗的高度明显高于其他光照时间下的各组。光照强度为35 µmol photons/m2·s时,盘状体萌发直立体的百分率以及孢苗的高度明显比其他光照强度下的高。研究表明,在舌状蜈蚣藻育苗生产中,可采取孢子刚附着时静水培养,附苗后15 d充气培养,并控制光照时间为8–10 h和光照强度为35 µmol photons/ m2·s。     

基于ADAMS的随动复合平衡抽油机动力仿真

介绍了随动复合平衡抽油机的结构和基本参数,对曲柄净扭矩的计算公式进行了推导,说明了利用ADAMS进行抽油机动力仿真的基本步骤,给出了模型的建立和加载的方法,并对仿真结果进行了分析。分析结果表明,与异相型曲柄平衡抽油机相比,随动复合平衡抽油机的动力性能得以改善,具有较好的节能效果。     

浅谈互通立交连接部出入口设计

互通式立交端部设计是整个立交设计的重要部分,通过对端部出入口设计要点的分析研究,结合单、多车道出入口不同的设计要求,提出合理建议,以期更好的完善立交端部设计。     

Milk Protein Polymorphism in Kangayam Cattle

This paper reports the milk protein polymorphism, the allele frequencies of variants and the possible linkages among various combinations of milk protein phenotypes in the Kangayam cattle of south India. Milk samples from 156 Kangayam cows were typed by starch gel and polyacrylamide gel electrophoresis for caseins and whey proteins, respectively. All the four milk protein components studied, _s1-casein, -casein, -lactoglobulin and -lactalbumin, exhibited polymorphism with high allele frequencies of 0.9231±0.0151 for _s1-casein C, 0.9263±0.0148 for -casein A, 0.9135±0.0159 for -lactoglobulin B and a relatively high frequency of 0.6218±0.0275 for -lactalbumin A. The mean heterozygosity estimated over all the four milk protein loci was 0.2420. Genetic equilibrium was observed among all the loci studied, except -lactalbumin. Linkage analysis confirmed the non-independence between _s1- and -caseins and between caseins and -lactalbumin phenotypes.     

Towards the first linkage map of the<Emphasis Type="Italic">Didymella rabiei</Emphasis> genome

A genetic map was developed for the ascomyceteDidymella rabiei (Kovachevski) v. Arx (anamorph:Ascochyta rabiei Pass. Labr.), the causal agent of Ascochyta blight in chickpea (Cicer arietinum L.). The map was generated with 77 F₁ progeny derived from crossing an isolate from the U.S.A. and an isolate from Syria. A total of 232 DAF (DNA Amplification Fingerprinting) primers and 37 STMS (Sequence-Tagged Microsatellite Site) primer pairs were tested for polymorphism between the parental isolates; 50 markers were mapped, 36 DAFs and 14 STMSs. These markers cover 261.4cM in ten linkage groups. Nineteen markers remained unlinked. Significant deviation from the expected 1:1 segregation ratios was observed for only two markers (Prob. of χ²<0.05). The implications of our results on ploidy level of the asexual spores are discussed. http://www.phytoparasitica.org posting Sept. 5, 2002.     

Analysis of FMO genes and off flavour in pork

Off flavours in pork sometimes produce tastes such as sourness, fishy, metallic or other non‐typical flavours and are often caused by low pH. Loss of function mutations in flavin containing mono‐oxygenase 3 (FMO3) are known to be associated with a fishy off flavour in both chicken eggs and cow's milk and a similar autosomal recessive disorder is present in humans resulting in a fishy odour. FMO3 is a member of a gene family that is clustered on human chromosome 1. Comparative mapping suggested that FMO3 and the remaining FMO genes (ex. FMO1 and FMO5) might map to the orthologous region on pig chromosome 9 (SSC9) where a quantitative trait locus (QTL) for off flavour was previously identified. Primers were designed to amplify FMO1, FMO3 and FMO5 gene fragments and several SNPs were discovered and genotyping tests developed. The genotypes from the Iowa State University Berkshire × Yorkshire resource population were used to linkage map FMO1 and FMO3 to SSC9 and FMO5 to pig chromosome 4 (SSC4). QTL and associations analyses were performed using the map containing FMO1 and FMO3. Results demonstrated that FMO3 and FMO1 mapped less than 1 cM away from the peak for the off flavour QTL previously detected on SSC9 and provide indications of an association between the FMO3 polymorphism and off flavour in pork.     

微卫星标记与考力代羊体重体尺性状遗传关系研究

本试验用单标记法研究考力代绵羊1号染色体ILSTS004~CSSM004和BM6506~MCM130之间的12个微卫星位点ILSTS004、MCMA008、MNS0094、CSSM004、BM6505、BMS4008、CSRD0298、TGLA415、BM8246、RM0509、URB0038、MCM0130,与其绵羊初生重、断奶重、体重(8月龄)、体高、体长、胸围、管围的遗传关系,结果ILSTS004位点不同基因型对初生重影响极显著(P<0·01)、对体重影响显著(P<0·05),CSSM004位点对体长影响显著(P<0·05),其余位点对体重等性状无显著影响(P>0·05)。其中,ILSTS004位点:基因型101099个体的初生重显著高于基因型095093(P<0·05),基因型101099个体的体重显著高于基因型103103(P<0·05);CSSM004基因型196196个体的体长显著大于基因型202202(P<0·05)。提示在1号染色体微卫星位点ILSTS004附近可能存在影响绵羊初生重、体重的数量性状位点(QTL),ILSTS004可作为其遗传标记之一;在CSSM004附近可能存在影响体长的QTL,CSSM004可作为其遗传标记之一。     

强震作用下双层球面网壳结构非线性动力响应分析

针对大跨网壳结构的动力特性,提出了在强烈地震作用下双层球面网壳结构的非线性分析和结构动力稳定性判别方法.单元模型中考虑几何非线性和材料非线性的双重影响.分析时,以静力荷载作用下的受力状态作为时程分析的初始状态,采用B-R判断准则确定其临界荷载,通过加速度峰值-结构最大位移曲线来判别结构的动力稳定性,据此找出其动力失稳临界点及破坏规律.通过算例验证了本文方法的有效性.分析结果表明,双层球面网壳结构考虑双重非线性是必要的;一致缺陷模态对结构承载力的影响比振型模态缺陷的影响大.     

Ferguson机构动态测试确定运动曲线的起点

Ｆｅｒｇｕｓｏｎ机构动态性能检测非常重要高精度的检测必须由精确确定运动曲线起点作保证。本文提出实时找出点小邻域和离线数据处理逼近真实起点相结合的方法，分析了相应的系统误差，并给出了实验计算数据，该方法用于实验检测系统中取得较好效果。