不同阶段猪用颗粒饲料物理性能的对比分析

对某饲料厂不同阶段猪用4种颗粒饲料的物理性能包括直径、长度、硬度、容重、含粉率和耐久性指数（Pellet Durability Index, PDI）等进行测定,对结果进行归类总结并采用统计学的方法参照有关标准进行分析。结果表明,4种颗粒饲料直径在2.87~3.94 mm之间,母猪料直径最大,小猪料最小,两两之间差异显著（P<0.05）,而且随着猪只年龄的增加,颗粒饲料的直径呈递增趋势。颗粒长度在8.62~11.94 mm之间,以大猪料最长,小猪料最短,长径比偏高。颗粒硬度在3.86~6.47 kg之间,以大猪料最大,小猪料最小,中小猪料显著低于大猪料和母猪料（P<0.05）,只有小猪料符合有关要求。颗粒容重在576.7~614.6 g/L之间,母猪料最大,小猪料最小,两两之间差异显著（P<0.05）,与直径呈相同的增减趋势。含粉率以小猪料最大,且只有小猪料与大猪料之间差异显著（P<0.05）。颗粒PDI以大猪料最大,小猪料最小,各阶段猪料的含粉率和PDI均符合有关要求。建议饲料厂家注重颗粒饲料物理性能指标的控制,调整饲料配方和工艺参数,不断改进颗粒饲料的质量。     

原木灵芝孢子粉和浸膏粉中的牛磺酸

采用热水提取－磺基水杨酸沉淀法进行样品的前处理，利用氨基酸自动分析仪测定供试样品的牛磺酸含量。试验结果表明，原木灵芝孢子粉和破壁孢子粉中牛磺酸含量分别为8．44mg/100g-9.23mg/100g和7．34mg/100g-7.89mg/100g，而灵芝浸膏粉中牛磺酸含量高达140．82mg/100g-157.38mg/100g.     

羔羊全营养代乳粉对羔羊增重影响的试验

为了研究羔羊出生后采取人工饲喂代乳粉溶液的效果，对10日龄羔羊称重，以平均日增重与母乳组比较，用t检验方法检验差异显著性。研究结果显示羔羊平均日增重试验组为0.097-0.126kg，母乳组为0.071-0.113kg，二者没有显著差异。在生产中，代乳粉能替代绵羊母乳饲喂羔羊，对多胎品系羊的推广应用以及解决绵羊缺乳、少乳或无乳问题具有重要意义。     

酮粉法检测泌乳牛尿酮乳酮的应用研究

荷斯坦泌乳牛尿、乳酮体的酮粉法定性试验表明：尿酮阳性率为29．25％，乳酮阳性率为10％。尿、乳阳性牛的血酮、血糖、乳酮、尿酮定量测定表明：酮粉法判定泌乳奶牛亚临床酮病，尿酮阳性反应具有早期、敏感、准确性低的特点。乳酮阳性反应具有准确、敏感性低、方便等特点。二者同时定性检测具有互补作用。     

烤烟适宜施氮量试验初报

试验结果表明,烤烟施氮量以90.0~112.5kg/hm2为佳,在此条件下,烤烟的产量和产值最高。     

纤维板表面粉末涂料的涂饰工艺

研究一种在纤维板表面进行粉末涂装再转移印花的新工艺.结果表明:纤维板粉末涂装基材预处理采用预热干燥,表面砂光,控制含水率为6%～8%;喷涂上粉量为333.33～388.89 g·m-2;固化条件为180 ℃,15～25 min.采用干燥箱中热转移方式,转移印花温度为(160±10)℃,时间15～20 min.按GB/T 4893-85和GB/T1733-79测试涂膜性能,涂膜附着力等级为2级,耐磨性等级为1级,耐水性合格,耐液性等级为1级.图1表4参9     

二化螟群集性的调查研究

通过对二化螟群集性的调查分析,初步查明在不同类型田、水稻的不同生育期、二化螟幼虫的不同龄次,二化螟幼虫的群集性不同.这为科学制订二化螟防治指标提供了理论依据。     

降低人造板热压机液压系统油液污染的探讨

车间粉尘与湖湿空气是人造板热压机液压系统油液外界污染的主要原因，通过构筑封闭式泵房，增设辅助油箱，改变没箱底部结构，设置排污，排水装置，可有效降低人造板热压机液压系统油液污染，改善液压系统性能，提高压机工作效率。     

Biochemical properties of the pathogenesis-related proteins from tobacco

This review describes the discovery and identification of the pathogenesis-related proteins (PRs) from tobacco. In crude leaf extracts the PRs are distinguished from the proteins in uninfected plants by their solubility at pH 3, resistance to a range of proteases, and mobility in polyacrylamide gels upon electrophoresis (PAGE) in non-denaturing conditions. PAGE has been used as a qualitative and semi-quantitative assay for PRs, and their migration in gels made from different acrylamide concentrations has been used to identify charge and size isomers and electrophoretically identical PRs in different tobacco cultivars. The subunit composition and molecular weight (mol. wt) of the four PRs identified first in Xanthi-nc were determined by SDS-PAGE; staining the gels has shown that these same four proteins in Samsun NN did not contain carbohydrate, lipid or nucleic acid, nor were they isozymic forms of twenty five enzymes known to increase in activity following infection with TMV. Evidence suggests that most of the PRs in Xanthi-nc and Samsun NN are extracellular.The purification of several PRs from Xanthi-nc, Samsun NN and other tobaccos is described, as well as their mol. wt, subunit and amino acid composition. PRs 1a, b and c consist of a single polypeptide and have similar mol. wt and amino acid compositions. Antisera prepared against purified Xanthi-nc b₁ protein have been used to determine serological relationships between PRs and form the basis of a very sensitive quantitative assay using ELISA. The regulation of synthesis of some PRs has been shown to involve translational control.     

Some coat protein constituents from strawberry latent ringspot virus expressed in transgenic tobacco protect plants against systematic invasion following root inoculation by nematode vectors

The coding sequences in RNA2 for the coat proteins (CP) of strawberry latent ringspot virus (SLRSV) were modified and amplified using polymerase chain amplification reactions (PCR) to facilitate their expression inAgrobacterium tumefaciens-transformedNicotiana tabacum Xanthi-nc. The coding sequences for the smaller capsid protein (S, 29kDa) and that for the theoretical precursor of L and S (P, 73kDa) had ATG initiation codon sequences added at the 5-proximal Ser/Gly (S/G) cleavage site in the unmodified sequence. The sequence coding for the larger of the two proteins of mature SLRSV capsids (L, 44kDa) had an ATG codon added at its 5 S/G site and a TAG stop codon sequence added at the 3-proximal S/G site. The P, L and S proteins were expressedin planta to a maximum concentration of 0.01 % of total extractable proteins but did not assemble into virus-like particles. When challenged by mechanical inoculation with virus particles or viral RNA, and compared with control plants, tobacco plants (primary transgenic clones or S1 and S2, kanamycin-resistant seedlings) expressing the virus capsid subunits separately, or their precursor, decreased the accumulation of SLRSV particles in inoculated leaves and fewer plants became invaded systemically. In experiments in which the roots of seedlings were exposed to SLRSV-carrying vector nematodes (Xiphinema diversicaudatum), SLRSV was detected in the roots of non-transformed control tobacco plants (6/20) and in transgenic tobacco expressing the L protein (7/40), but not in any of 25 tobacco plants expressing the S protein or in 35 expressing the P protein. This is the second example of CP-mediated resistance to virus inoculation by nematode vectors.