Porcine reproductive and respiratory syndrome virus: morphological, biochemical and serological characteristics of Quebec isolates associated with acute and chronic outbreaks of porcine reproductive and respiratory syndrome.

Cytolytic and noncytolytic strains of the porcine reproductive and respiratory syndrome virus (PRRSV) were isolated in primary cultures of porcine alveolar macrophages (PAM) from lung homogenates of stillborn fetuses or blood samples of dyspneic piglets collected from Quebec pig farms having experienced acute or chronic outbreaks of PRRS. Serological identification of the virus was confirmed by indirect immunofluorescence and indirect protein A-gold immunoelectron microscopy using reference antiserum prepared from experimentally-infected specific pathogen free (SPF) piglets and monoclonal antibodies (MoAbs) directed against the p15 nucleocapsid (N) protein of the reference ATCC-VR2332 isolate. Intracytoplasmic enveloped viral particles that tended to accumulate into cytoplasmic vesicles were observed in the infected PAM; no budding was demonstrated at the level of the cytoplasmic membrane. The extracellular virions appeared as pleomorphic but mostly spherical enveloped particles, 50-72 nm in diameter (averaged diameter of 50 particles was 58.3 nm), with an isometric core about 25-30 nm. Buoyant density of the virus in CsCL density gradients was estimated to 1.18-1.20 g/mL. No hemagglutinating activity was demonstrated. Analysis of semipurified virions of isolate IAF-exp91 by radioimmunoprecipitation (RIPA) and Western immunoblotting experiments, using reference rabbit and porcine hyperimmune sera, revealed four major viral proteins, a predominant 15 kD N protein and three other proteins with predicted M(r_ of 19, 26 and 42 kD. Progeny viral particles produced in PRRSV-infected PAM in the presence of tunicamycin lacked the 42 kD protein, thus confirming its N-glycosylated nature. Immunoprecipitation experiments using the anti-ATCC-VR2332 MoAbs confirmed the close antigenic relationships between Quebec and American reference isolates of PRRSV.     

马鹿假台鹿采精技术的研究

对６头试验公鹿用假台鹿采精，采精前对特制的假阴道以药用凡士林为滑润剂，注水充气，温度为４０℃±１℃，以适宜的压力和滑润度，将其安装在人工制做的假台鹿内。拨赶公鹿于采精场诱其爬跨。结果，试验的６头公鹿中有４头能够采精，共２２头次，射精量平均每头次１．５４ｍｌ，精子密度为１８．６—３７亿／ｍｌ，精子活力在０．８以上。９３年每头次生产细管冻精１０６．２５支（４２５支／４头次），是同年电刺激采精法平均６４．４支／头次（９０２支／１４头次）的１．６５倍，此法既能采到质量高的精液，又比电采法省工、省时、省力、安全，是一种理想的马鹿采精方法。     

PEG诱导水分胁迫对柑桔幼苗细胞质膜透性及脯氨酸含量的影响

柑桔叶片相对含水量(RWC)随聚乙二醇(PEG)处理渗透势的降低而依次降低;叶片细胞质膜透性随PEG处理浓度的增加而依次增大;幼苗叶片累积脯氨酸的数量随水分胁迫时间和强度递增。     

如东县鸡腿病病因的调查研究

本文对如东县４０个养鸡户的鸡腿病进行了门诊与跟踪调查。从传染病、营养代谢病及饲养管理三个方面对发病原因进行了初步的探讨。结果表明：营养缺乏和代谢紊乱（特别是钙、磷）是该县鸡腿病的主要原因，传染性腿病如疑似病毒性关节炎、禽脑脊髓炎、葡萄球菌性关节炎等也不容忽视。     

β-葡聚糖对啤酒易滤性影响的研究

通过对啤酒中β-葡聚糖的定性定量分析和啤酒易滤性的测定,发现溶解状态的β-葡聚糖对啤酒的过滤没有明显的影响,而β-葡聚糖凝胶对啤酒过滤有严重影响.啤酒中β-葡聚糖凝胶的分子量在300 000以上,当含量达到20 mg/1时,就会使啤酒膜过滤困难.啤酒的易滤性与β-葡聚糖含量之间里r=-0.222的不显著负相关,而与β-葡聚糖凝胶的含量之间呈r=-0.841~(***)的极显著负相关.     

不同环境下作物基因型值和杂种优势的分析方法

根据加性－显性与环境互作的遗传模型，提出了利用多个环境的杂交亲本和Ｆ＿１的资料，采用ＡＵＰ法预测作物杂种后代在不同环境中的基因型值和杂种优势的分析方法。作为分析实例，本文对１９９２年和１９９３年陆地棉（ＧｏｓｓｙｐｉｕｍｈｉｒｓｕｔｕｍＬ．）杂交亲本（Ｐ）、Ｆ＿１皮棉产量和衣分的两年资料进行了分析。     

两种一年生植物在替代试验中的相互竞争关系

（1）用替代试验研究了燕麦（Aneva sativa）和箭舌豌豆（Vicia sativa）在混播中的竞争相互作用。为了攻混播比例对两种植物在混播条件下的行为影响，田间试验设为5个混播总密度和5种混播比例，共了5次。（2）方差分析表明，相对总生物量（RYT）和竞争平衡指数（CBI）对总密度，混播比例和生长时间的反应敏感。总密度对RYT和CBI的影响高度显著，在大多数情况下，混播比例对RYT和CBI的影响不显著。（3）本文研究的结果表明，持续时间对RYT和CBI很强的影响，在第1次测定时，RYT值接近1而BI值接近0，这一事实表明，种间无竞争或互惠作用。而在生长旺盛期，种间竞争较为剧烈。（4）本研究结果表明，箭舌豌豆的生长严惩受到燕麦的抑制作用，这说明箭舌豌豆在与燕麦混播时表现为竞争上的弱者。     

河北省桑属植物染色体倍数性研究

研究了桑属植物５个种３２个品种的染色体倍数性，发现宽城１０号等９个品种为三倍体（２ｎ＝３ｘ＝４２），其余为二倍体（２ｎ＝２ｘ＝２８）。