日光温室不同生育期嫁接番茄对根际环境及生长特性的影响

实验以不同砧木嫁接番茄在不同时期根系环境对生长发育的影响研究。结果表明,随着嫁接番茄的生长发育,根际环境也变化。一般情况下,在结果期,放线菌数量较多。植株根系活力大、土壤K、Ca、Mg、Zn含量多、拉秧期细菌数量较大的嫁接番茄,生长势强。     

旋转栅对脱油型旋流器流场影响的数值分析

根据计算流体力学方法,利用雷诺应力湍流模型和多相流模型中的混合物模型,对采用叶片式、螺旋式和通式3种不同旋转栅的脱油型动态旋流器流场分别进行数值模拟,以揭示旋转栅流道结构对动态旋流器流场的影响。结果表明:旋转栅结构形式对动态旋流器内湍流强度和湍流耗散的影响非常大;螺旋式旋转栅可以降低动态旋流器内旋转栅附近的湍流强度,但对旋流器内整个流场湍流的改善并不明显;与叶片式和螺旋式旋转栅相比,通式旋转栅所产生的切向速度和轴向速度较大,具有更强的分离能力和更宽的高效分离域。     

中宁县影响红枣产量的主要农业气象灾害分析

通过对试验基地中宁1981—2008年气象资料和红枣产量资料的分析,结合历年主要农业气象灾害记录,得出了5类影响红枣产量的主要农业气象灾害,分别是萌芽展叶期高温(B₁)、盛花期空气的高温低湿B₂)、盛花期连阴雨(B₃)、果实生长期连阴雨(B₄)、果实成熟期连阴雨(B₅);采用层次分析法对上述气象灾害进行量化分析,得到其对红枣生产的影响权重顺序：B₅>B₄>B₂>B₃>B₁;将趋势产量 进行灾害订正,预测红枣各生育期的实际产量,并建立了基于农业气象灾害的中宁红枣的动 态产量预报模型,可为实际预报业务提供参考依据。     

播娘蒿油酸脱氢酶基因(DsFAD6)的克隆和表达分析

采用RACE-PCR的技术克隆了播娘蒿的油酸脱氢酶基因(DsFAD6),它是催化油酸转化为亚油酸的一个关键酶基因.DsFAD6 cDNA全长序列的开放阅读框长1 344 bp,编码一个由447个氨基酸残基组成的蛋白质,推测的蛋白质相对分子质量为51.16 kD,等电点为9.27.序列分析表明DsFAD6的氨基酸序列具有3个高度保守的组氨酸盒子,该结构在去饱和酶中是高度保守的,且在N端预测到信号肽,初步认定该酶定位于质体.序列比对和系统发生分析显示DsFAD6与十字花科植物FAD6基因具有较高一致性.RT-PCR分析表明,DsFAD6在根、茎、叶、花蕾、花及幼嫩角果中均表达,但在茎、叶和幼嫩角果中表达较高.胁迫诱导表达中,DsFAD6在播娘蒿叶片中表达明显受伤害胁迫诱导,但在冷胁迫下呈负相关.     

同安钮夜蛾幼虫空间分布及其防治药剂研究

对同安钮夜蛾(Anua indiscriminata Moore)幼虫在桉林的分布进行了调查,并在室内测试了几种农药对其幼虫的毒性,结果表明,同安钮夜蛾幼虫在林间为聚集分布;其虫口密度在同一树冠不同方向或层次上的分布差异不显著;坡向对同安钮夜蛾幼虫的分布影响显著,南坡的虫口密度高于北坡的。在供试的农药中,25%灭幼脲Ⅲ号悬浮剂0.67 g/L液、1.8%阿维菌素乳油0.25 g/L液、保尔或锐劲特0.5 g/L液、0.3%印楝素乳油2 g/L液、1.3%鱼藤氰乳油或10%吡虫啉可湿性粉剂1 g/L液对同安钮夜蛾5～6龄幼虫的毒杀效果均达96%以上。     

Antigenic differences between H5N1 human influenza viruses isolated in 1997 and 2003

To assess whether the antigenic properties of H5 hemagglutinin (HA) change over time due to antigenic drift, we produced a panel of monoclonal antibodies (mAbs) against the HA of the index H5N1 human influenza A virus, A/Hong Kong/156/97. By immunizing mice with a plasmid expressing this HA and boosting the initial immunization with cell lysates transfected with the plasmid, a total of six hybridomas producing HA-specific mAbs were established: four to the HA1 subunit with hemadsorption-inhibiting activity and two to the HA2 subunit. None of the mAbs to HA1 could bind to the HA of a recent human isolate, A/Hong Kong/213/2003, indicating that there are substantial antigenic differences between the H5N1 human influenza virus isolated in 1997 and that isolated in 2003.     

Molecular cloning, in vitro expression and bioactivity of goose B-cell activating factor

B-cell activating factor (BAFF), belonging to the TNF family, is critical for B cell survival and maturation. cDNA of goose BAFF (gBAFF) was amplified from goose spleen by RT-PCR. The open reading frame (ORF) of gBAFF encodes a protein of 288-amino acid. The gBAFF shows 98, 92, 44 and 55% amino acid sequence identity with duck (dBAFF), chicken (cBAFF), mouse (mBAFF) and human BAFF (hBAFF), respectively. RT-PCR results showed that gBAFF mRNA is expressed in thymus and more highly expressed in the bursa of Fabricius and spleen. Recombinant soluble gBAFF (gsBAFF) expressed in Escherichia coli has molecular weight of approximately 19kDa. In vitro, purified gsBAFF was able to promote bursa B cells survival/proliferation in goose, duck and chicken. Furthermore, recombinant dsBAFF and csBAFF have a positive effect on goose, duck and chicken bursa B cells survival/proliferation. These findings indicate that gBAFF plays an important role in the survival/proliferation of goose B cells and, owing to its high evolutionary conservation, functional cross-reactivity exists between chicken, duck and goose BAFF.     

Rapid identification and differentiation of Theileria sergenti and Theileria sinensis using a loop-mediated isothermal amplification (LAMP) assay

The present study developed and validated a species-specific loop-mediated isothermal amplification (LAMP) assay for the rapid detection and discrimination of two benign bovine Theileria species – T. sergenti and T. sinensis. The LAMP assay is inexpensive and easy to perform and involves a rapid reaction-the amplification can be performed in 55 min or 50 min under isothermal conditions of 61 °C or 63 °C, respectively, by employing a set of four species-specific primer mixtures. The results can be checked using agarose gels. The optimal assay conditions, under which the assay exhibited with no cross-reaction with other closely related tick-borne parasites (T. annulata, Babesia bovis, B. bigemina, B. major, B. ovata, B. U. sp., Anaplasma marginale) or between the two Theileria species of interest, was established. The assay is approximately 10-fold more sensitive than the conventional specific PCR assay. The LAMP assay was validated using DNA from 6 standard stocks in the laboratory and was evaluated for its diagnostic utility using blood samples collected from experimentally and naturally infection cattle or yaks in China. These findings indicate that this Theileria species-specific LAMP assay may have potential clinical applications for the detection and differentiation of two benign bovine Theileria species – T. sergenti and T. sinensis, especially in endemic countries.     

犬嗅认嗅源能力的培养

嗅认嗅源能力的培养是一个缓慢的过程,需要训犬员长期不懈的训练培养才能形成。嗅认嗅源其实也是犬对训犬员的服从,因此对嗅认嗅源的训练应该先于追踪、鉴别等使用科目,并且贯穿于整个训练的始终。     

Plasma concentrations of testosterone and nandrolone in racing and nonracing intact male horses

Pennsylvania (PA) State Racing Commissions regulate the endogenous androgenic steroid, testosterone (TES), in racing intact males (RIM) by quantification of TES in post-race samples. Post-race plasma samples (2209) collected between March 2008 and November 2010 were analyzed for TES, nandrolone (NAN), and other anabolic steroids (ABS). Of the 2209 plasma samples, 2098 had quantifiable TES ≥ 25 pg/mL. Plasma (mean ± SD) concentrations of TES and NAN in RIM were 329.2 ± 266.4 and 96.0 ± 67.8 pg/mL, respectively. Only 64.6% of RIM had quantifiable concentration of NAN, and there was no relationship between TES and NAN. Plasma TES concentrations were significantly (P < 0.0001) higher during the months of April, May, June, July, and August. A significantly higher (P < 0.006) plasma TES was observed in Thoroughbred (TB) (347.6 ± 288.5 pg/mL) vs. that in Standardbred (STB) (315.4 ± 247.7 pg/mL). Plasma concentrations of TES from breeding stallions (BS) were 601.6 ± 356.5 pg/mL. Statistically significant (P < 0.0001) lower plasma concentrations of the two steroids were observed in RIM horses. Based on quantile distribution of TES in the RIM and BS populations, 99.5% were at or below 1546.1 and 1778.0 pg/mL, respectively. Based on this population of RIM, the suggested upper threshold plasma concentration of endogenous TES in horses competing in PA should remain at 2000 pg/mL.