银川地区羊肝中阿苯达唑(丙硫苯咪唑)残留情况的调查

阿苯达唑又称丙硫苯咪唑或丙硫咪唑，有时又称抗蠕敏，是目前国内常用的驱虫效果好、范围广、毒性较低的兽用驱虫药。随着家庭舍饲养羊规模的不断扩大，饲养者为了减少因寄生虫导致的死亡并增加育肥效果，常把阿苯达唑作为育肥前预防驱虫或寄生虫病治疗的首选药，出现了滥用或超剂量使用的现     

播量对水稻生长发育及干物质积累的影响

用盆栽方法进行播量对寒地水稻生长发育及干物质积累影响试验,结果表明:稀播的秧苗发根力强、分蘖多、茎基宽、充实度高。播量200g/m2的产量最高。     

Crystalluria. Observations, interpretations, and misinterpretations

Crystalluria results from oversaturation of urine with crystallogenic substance. However, oversaturation may occur as a result of in vitro as well as in vivo events. The microscopic appearance of crystals only represents a tentative identification of their composition because variable conditions associated with their formation, growth, and dissolution may alter their appearance. Definitive identification is dependent on physical methods such as optical crystallography, x-ray diffraction, and electron microscopic analysis.     

完善农村居民最低生活保障制度的几点建议

当前，我国农村普遍建立了居民最低生活保障制度，这是保障农村社会稳定的“最后一道安全网”，是中国农村社会保障体系的基础工程。但是，我国农村居民最低生活保障制度也还存在一些问题，例如保障对象、保障方式、保障资金、管理体制等，充分认识并采取 有效措施解决好这些问题，对于完善农村社会保障体系，维护农村社会稳定和经济发展有着重要现实意义。     

S1核酸酶突变检测法的优化

优化了S1核酸酶突变检测体系,结果表明(1)扩增法比杂交法产生异源双链DNA更节省时间;(2)PCR产物可以直接作为突变检测的底物;(3)适当降低反应温度、适当增加反应缓冲液中的NaCl浓度、适当缩短反应时间可提高突变检测效果。     

沙黄松选择增益结构模式初步研究

采用沙黄松天然林自由授粉家系７年生树干材积的材料，分析了联合选择遗传增益结构模式。结果表明：亚群体间存在极显著差异，亚群体内家系间差异不显著；联合选择增益结构模式为亚群体间７２．４４％、亚群体内家系间３．５５％、单株间２４．０１％。     

Acid-induced autoagglutination found in chicken pathogenic Escherichia coli strain.

Chicken pathogenic Escherichia coli strains were found to autoagglutinate in a static culture of trypticase soy broth (TSB). One strain, designated PDI-386, was further studied for its autoagglutinating property. Acidity in the cultured medium caused by glucose degradation induced the autoagglutination. The bacterial cells grown in a glucose-free L-broth could be aggregated by adding acid, which suggests a potentiality of autoagglutination of the strain grown in the L-broth. The autoagglutinating parent (Agg) formed small colonies with irregular edges like rough colonies on the TS agar, whereas its non-autoagglutinating variant (Nag) formed larger smooth colonies with a perfectly round edge. The Nag colony was easily generated from the Agg colony on the TS agar. The autoagglutinating property was very unstable when the bacteria was passed in the TSB, but rather stable in the L-broth. Under electron microscope, the Agg were found to possess pili of more than 20 microns in length. However, the phenotypic expression of autoagglutination did not correlate with that of mannose-sensitive hemagglutination against guinea pig erythrocytes. Incubation of the Nag in the L-broth at room temperature for more than 10 days provoked the reversion of the autoagglutination. There was no difference between the Agg and the Nag in terms of surface hydrophobicity, sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) patterns of membrane proteins and LPS, and plasmid profiles. The virulence of the Agg was higher than that of the Nag. The autoagglutination property is, however, so unstable that the pathogenicity of E. coli isolates from chickens should be carefully evaluated.     

Inherited hyperchylomicro-naemia in the cat: Lipoprotein lipase function and gene structure

Hyperchylomicronaemia was identified in a four-week-old Siamese kitten with lethargy, in-appetence, hindlimb ataxia and profound anaemia. The kitten was euthanased and at necropsy a thrombus was found occluding the caudal aorta. Two littermates later presented with lethargy, inappetence and hypertriglyceri-daemia which resolved after being weaned on to a low fat diet. A similar condition was subsequently diagnosed in a kitten born to the same sire but a different queen. The expression of hyperchylomicronaemia in two related litters was suggestive of an inherited, familial defect in the function of lipoprotein lipase (LPL). The activity of this enzyme was reduced in all three parents, the two recovered cases and two related, but apparently unaffected kittens, compared with a control group of unrelated cats belonging to the breeder. This reduction in activity was not attributable to defective activation of LPL by its serum cofactor apolipoprotein C-II or the presence in plasma of a factor that inhibited LPL. The gene that codes for LPL was examined by restriction fragment length polymorphism analysis using a human LPL cDNA probe. The results showed that the cat has a similar, but not identical, LPL gene to man. However, there were no differences in the restriction fragment patterns obtained from affected, unaffected and control animals.