柑橘褐斑病菌对不同抗性柑橘品种防御酶活性的影响

以柑橘褐斑病高抗品种Lw8,中抗品种L2,高感品种Lw14为实验材料,通过孢子喷雾法使柑橘褐斑病菌感染柑橘叶片,研究接菌0d、1d、2d、3d、6d、8d、10d时,柑橘叶片中超氧化物歧化酶(SOD)、过氧化物酶(POD)、过氧化氢酶(CAT)、苯丙氨酸解氨酶(PAL)、多酚氧化酶(PPO)、几丁质酶(CHT)酶和β-1,3葡聚糖酶(GLU)含量及活性变化规律与品种抗病性的关系。结果表明,接种前,两个抗病品种Lw8、L2中的POD、SOD、PAL、PPO 、GLU、CHT活性显著高于高感品种Lw14,CAT活性则与高感品种Lw14相近;接种后,3个不同抗性品种中SOD、POD、CAT、PAL、PPO 、GLU、CHT 7种防御酶活性较对照明显提高,但不同品种增加幅度不一致,除CAT外,其余6种防御酶活性均表现为抗病品种Lw8、L2增幅显著高于高感品种Lw14,且两个抗病品种一般在接菌3d内6种防御酶活性迅速升高并达到峰值;而高感品种Lw14防御酶(除CAT外)活性或增幅较小或较两个抗病品种滞后。本研究初步探讨了不同抗性品种接种褐斑病菌后7种防御酶的活性动态变化与柑橘品种抗病性关系,为进一步研究其抗病机理奠定基础。     

红肉猕猴桃果园管理技术概述

红肉猕猴桃是猕猴桃中的特色类群。红肉猕猴桃品种在消费市场需求旺盛,商业价值突出,商业栽培面积快速增加,但产业发展中的技术问题也日益突出。本文就红肉猕猴桃产业发展的基本环境和现状、果园生产的技术问题及解决方案等做一概述,以期为红肉猕猴桃产业健康持续发展提供建议。     

植物生长调节剂、基质对三个品种费约果扦插生根的影响

选取五年生健壮费约果树为母株,采用L9(33)正交设计法研究植物生长调节剂、基质对三个品种费约果半木质化枝条扦插生根的影响。本试验结果表明：不同品种、植物生长调节剂和基质处理的生根的影响呈显著性水平。影响费约果扦插枝条生根率因素的主次顺序为品种>植物生长调节剂>基质;影响根长因素的主次顺序为基质>植物生长调节剂>品种;影响插穗根数的因素主次顺序品种>基质>植物生长调节剂。Gemini品种经1000 mg/L ABT浸泡两分钟,以腐叶土+珍珠岩为基质,生根效果最好,生根率为70.00%,平均根长为8.85 cm,平均根数为10.22条/穗;Unique品种经1000 mg/L ABT浸泡两分钟,以腐叶土+蛭石为基质,生根效果较好,生根率为56.67%,平均根长为9.32 cm,平均根数为12.33条/穗;Coolidge品种生根率低,均≤20 %。     

河北省天然草地禾本科植物的生活型、生态型及区系分析

对河北省天然草地禾本科植物的生活型、生态型及区系特征进行了分析，结果表明，多年生草本为优势生活型，占78．4％；生态型以中生植物为主，占77．2％，旱生植物占16．0％，湿生植物仅占6．8％；植物区系成分多样，温带分布属最多达42属，占总属数的57．5％，其次为热带分布属，有24属，占32．9％。     

Report on the analyses of mAb reactive with porcine CD8 for the second international swine CD workshop

Based on an analysis of their reactivity with porcine peripheral blood lymphocytes (PBL), only three of the 57 mAbs assigned to the T cell/activation marker group were grouped into cluster T9 along with the two wCD8 workshop standard mAbs 76-2-11 (CD8a) and 11/295/33 (CD8b). Their placement was verified through the use of two-color cytofluorometry which established that all three mAbs (STH101, #090; UCP1H12-2, #139; and PG164A, #051) bind exclusively to CD8⁺ cells. Moreover, like the CD8 standard mAbs, these three mAbs reacted with two proteins with a MW of 33 and 35 kDa from lymphocyte lysates and were, thus, given the wCD8 designation. Because the mAb STH101 inhibited the binding of mAb 76-2-11 but not of 11/295/33, it was given the wCD8a designation. The reactivity of the other two new mAbs in the T9 cluster with the various subsets of CD8⁺ lymphocytes were distinct from that of the other members in this cluster including the standards. Although the characteristic porcine CD8 staining pattern consisting of CD8^low and CD8^high cells was obtained with the mAb UCP1H12-2, a wider gap between the fluorescence intensity of the CD8^low and CD8^high lymphocytes was observed. In contrast, the mAb PG164A, not only exclusively reacted with CD4⁻/CD8^high lymphocytes, but it also failed to recognize CD4/CD8 double positive lymphocytes. It was concluded that this mAb is specific for a previously unrecognized CD8 epitope, and was, thus, given the wCD8c designation. A very similar reactivity pattern to that of PG164A was observed for two other mAbs (STH106, #094; and SwNL554.1, #009). Although these two mAbs were not originally positioned in the T cell subgroup because of their reactivity and their ability to inhibit the binding of PG164A, they were given the wCD8c designation. Overall, five new wCD8 mAbs were identified. Although the molecular basis for the differences in PBL recognition by these mAbs is not yet understood, they will be important in defining the role of CD8⁺ lymphocyte subsets in health and disease.     

Comparison of 3 methods of selenium assessment in cattle.

Three tests are routinely done to assess blood status of selenium in cattle: serum selenium, whole blood selenium, and glutathione peroxidase. The objective of this study was to compare the various analytical methods for determining blood selenium status in groups of mature cows and beef calves. Twenty to 30 blood samples per herd were collected from 8 beef herds in central Alberta and 1 dairy in Alberta herd twice a year from the spring of 1992 through the fall of 1995, and once from 185 spring calves in 2 beef herds in Saskatchewan. Serum and whole blood samples were submitted to 1 laboratory and whole blood samples were submitted to a 2nd laboratory. Samples for glutathione peroxidase determinations were submitted to a 3rd laboratory. Pearson's correlation coefficients and Cohen's kappa were calculated for each possible comparison among the different measures. The best agreement was observed between serum and whole blood analysis within Laboratory A. The remaining comparisons reflected poor agreement. Comparison of herd-level assessment resulted in better agreement than comparison of individual sample results among laboratories and procedures for all combinations tested. Serum selenium analysis was the only laboratory procedure for which external reference material was utilized. Serum selenium, whole blood selenium, and glutathione peroxidase measure different compartments of the blood selenium pool. The time frame of interest, supplementation practices, and the stability of recent dietary intake determine the optimum assessment method for individual animals or herds. Determination of the serum status or of blood selenium is more consistently measured at the herd-level than for individual samples.     

青海省当归茎线虫种类鉴定

采集和分离到青海省大通县、互助县4个当归茎线虫群体,通过形态特征和测量值比较,以贝叶斯法构建ITS-rDNA系统发育树,并用4种内切酶DdeⅠ、HinfⅠ、Tru9Ⅰ(MseⅠ)和SduⅠ 进行ITS-RFLP分析。结果表明,青海省大通县、互助县当归茎线虫群体的形态特征与腐烂茎线虫（Ditylenchus destructor）基本一致,体长略小,雄虫尾长和c(体长/体宽)值略大,雌虫a(体长/尾长)值略大,其他测量值均与腐烂茎线虫模式种一致。通过rDNA-ITS序列系统发育分析,发现青海省大通县、互助县茎线虫群体与腐烂茎线虫群体聚为一支,但不能归为目前已知基因型。rDNA-ITS区段PCR-RFLP结果显示,青海省4个群体与已报道的腐烂茎线虫群体酶切结果不一致,且存在明显差异。经形态与分子生物学特征分析,将这4个线虫群体确定为腐烂茎线虫,表明该线虫已在青海省发生与分布。     

超高比表面积活性炭孔分布对天然气脱附量的影响

在比表面积相同的情况下,研究了超高比表面积活性炭吸附剂孔分布对天然气脱附量的影响.研究结果表明,超高比表面积活性炭吸附剂的中孔(2 nm相似文献   

Serodiagnostic comparison of enzyme-linked immunosorbent assay and surface plasmon resonance for the detection of antibody to Porcine circovirus type 2

This paper describes the cloning and expression of the capsid protein of Porcine circovirus type 2 (PCV2) in an Escherichia coli expression system that was used to produce a fusion protein for subsequent immunologic studies: enzyme-linked immunosorbent assay (ELISA) and surface plasmon resonance (SPR). Polymerase chain reaction was used to amplify the gene encoding the capsid protein from the DNA of PCV2. The protein was then cloned into a pRSET prokaryotic expression vector. Western blot analysis revealed that the recombinant protein gave strong signals on a polyvinylidene difluoride membrane when exposed to the serum from a pig infected with PCV2. The expressed protein was purified and used as an antigen for the ELISA and SPR study. A protein chip based on SPR was developed, and the diagnostic potential of SPR was compared with that of ELISA with the use of 70 serum samples obtained from 6 pig farms. There was a strong positive correlation between the ELISA and SPR titers (r = 0.877, P < 0.01). Therefore, this recombinant capsid protein can be used as an antigen for serologic studies, and the SPR, a label-free method, appears to be a valuable and reproducible tool in the serodiagnosis of a PCV2 infection.     

非圆斜齿轮滚切策略与实用模型性能分析

为实现非圆斜齿轮滚切加工,基于5轴联动滚切策略,应用运动学原理推导齿坯附加转动和滚刀附加转动2种方案的基本数学模型;采用工件等弧长、工件等转角和工件等极角3种方法简化该模型,构成6种滚切实现方案及实用模型;采用Matlab软件对6种模型进行五联动轴的(角)速度、(角)加速度动态性能分析,得出加工精度及效率高、动态品质综合性能较好的等弧长齿坯附加转动和等弧长滚刀附加转动2种最佳模型.经滚切试验验证了模型的正确性,齿面测试分析与仿真结论一致.