浅谈我国猪伪狂犬病的净化

伪狂犬病是由伪狂犬病毒(Pseudorabies vires，PRV)引起的多种家畜、野生动物、伴侣动物和实验动物的一种急性传染病。PRV在自然条件下能感染猪、牛、羊、犬、猫、兔、鼠、野猪、貂、熊、狐等动物。除猪以外，其它动物感染PRV后，出现发热、奇痒和急性脑脊髓炎等典型症状。猪是PRV的储藏者和传染     

营养液浓度及pH值对山葵生长及光合速率的影响

 探讨了0.5、1.0、1.5 倍日本园试营养液3 种浓度(以清水为对照) 和5.4、6.0、6.6、7.2 等4 种pH 值对山葵生长和光合速率的影响。结果表明, 在营养液1.0 倍和pH 6.0 条件下, 山葵平均根茎鲜质量为42.75 g , 且叶绿素含量和净光合速率显著高于其它处理。     

苯丙烯酸对黄瓜幼苗光合作用和细胞超微结构的影响

 通过基质栽培研究不同浓度的苯丙烯酸对黄瓜幼苗光合作用和超微结构的影响。结果表明，苯丙烯酸浓度在80 µmol·L 时显著地降低了黄瓜幼苗的叶面积、叶绿素a含量、光合速率、蒸腾速率、根系活力和气孔张开数(P<0.05)；叶绿体和线粒体等超微结构也受到破坏，而浓度在150 µmol·L 时显著减少了全株干质量和气孔总数，细胞器出现解体现象。     

铺散诸葛菜的组织培养及植株再生

 以铺散诸葛菜的叶柄及叶片为外植体, 研究了不同的再生方式。在6-BA 和NAA 配合使用的MS 培养基上, 叶柄和叶片外植体有高的成芽率, 具有强的器官再生能力。在2,4-D 与6-BA、NAA 结合的培养基上, 叶柄和叶片有较高的愈伤组织诱导率, 在含6-BA 的培养基上也易于分化。叶柄、叶片再生的芽和经愈伤组织分化而得来的芽快速繁殖后, 在生根培养基上形成完整植株。研究表明铺散诸葛菜具有极强的器官分化能力。     

应用真空熏蒸技术杀灭蔗扁蛾

利用真空熏蒸技术对受蔗扁蛾Opogona sacchari Bojer危害的发财树进行了真空熏蒸处理.结果表明,在真空条件下,仅需要较低的熏蒸剂量在较短的时间内即可全部杀死发财树里的蔗扁蛾,杀虫效果达100%,达到快速、高效、安全、环保的要求.为花卉害虫的处理提供了一种新的方法.     

不同光湿环境对葡萄花芽分化和叶绿体类囊体膜磷酸酯酶活性的影响

以欧亚种葡萄美人指(Vitisviniferacv.ManicureFinger)为试材,正常光湿为对照,采用正常光偏高湿、偏弱光正常湿度、偏弱光高湿、偏弱光临界高湿、临界弱光偏高湿和临界弱光临界高湿6种处理。试验表明:单一偏弱光处理,葡萄叶片叶绿素含量上升,其余处理叶绿素含量下降;6种处理叶绿体类囊体膜磷酸酯酶活性都低于对照,叶绿体类囊体膜磷酸酯酶活性与光照和湿度有关;正常光偏高湿和偏弱光正常湿度部分芽能分化花原基,但在偏弱光高湿或偏弱光临界高湿花芽分化质量严重下降,临界弱光偏高湿和临界弱光临界高湿几乎未发现花原基;单一的弱光因子比单一的高湿因子对叶绿体类囊体膜磷酸酯酶活性和花芽形态分化影响更大,但弱光与高湿同时存在比单一弱光或高湿因子作用于葡萄时,叶绿体类囊体膜磷酸酯酶活性下降更为显著,花芽更难以形成。     

不同副梢处理对赤霞珠葡萄生长和结果的影响

试验以3～5年生赤霞珠葡萄(CabernetSauvignon)为试材,对其进行了不同的副梢处理:只留顶端1个副梢、副梢绝后处理、花序以上反复摘心、副梢全留。2年的结果表明:副梢全留(所有副梢全留2～3片叶反复摘心)处理的叶面积指数高,果实的产量和品质高。因此,相对多留副梢叶片,改善了叶幕叶龄结构,提高了果实品质,有利于枝梢成熟。     

山杏新品种‘甜仁山杏’

 ‘甜仁山杏’是从山杏(苦杏仁) 中选出的甜仁新品种。其种子不具苦味, 果实、果核及种子比原变种小。可用于山区造林, 种子用于深加工。     

Functional heterogeneity in resources within landscapes and herbivore population dynamics

Large mammalian herbivores are notorious for their propensity towards population irruptions and crashes, yet many herbivore populations remain relatively stable. I explore how resource heterogeneity within landscapes dampens population instability, using a metaphysiological modelling approach considering patch state distributions. Resource heterogeneity is functionally stabilizing through spreading consumption away from preferred resources before these become critically depleted. Lower-quality resources act as a buffer against starvation during critical periods of the seasonal cycle. Enriching resource quality is destabilizing, even if patch diversity is maintained, because food quantity then becomes the limitation. The potential consequences of landscape fragmentation are explored using the Serengeti ecosystem, characterised by broadscale resource gradients, as a hypothetical example. Further insights provided by the model are illustrated with specific examples concerning the effects of patch scales and waterpoint distribution. A metaphysiological modelling approach enables the basic consequences of landscape heterogeneity to be distinguished from further effects that may arise from specific patch scales and configurations, without the distracting detail of spatially explicit models.     

Validation of the specificity and sensitivity of species-specific primers that provide a reliable molecular diagnostic for <Emphasis Type="Italic">Xiphinema diversicaudatum</Emphasis>, <Emphasis Type="Italic">X. index</Emphasis> and <Emphasis Type="Italic">X. vuittenezi</Emphasis>

Xiphinema diversicaudatum and X. index are vector nematode species of economic importance in viticulture regions as they can transmit Arabis Mosaic, Grapevine Fanleaf and Strawberry Latent Ringspot viruses to grapevine. Wang et al. (2003) designed species-specific diagnostic primers from ribosomal genes for both these vector species as well as a vector and a non-vector species X. italiae and X. vuittenezi, respectively. Our study aimed to confirm the specificity and determine the sensitivity and reliability of the primers for the two vector species, X. diversicaudatumand X. indexwhen challenged with closely related longidorid species and general nematode communities typical of vineyard soil. With one exception, no PCR product was observed when the primers were tested against six Longidorus, one Paralongidorus and one Xiphinema non-target species. Occasionally (three out of eight replicate PCR reactions) a weak PCR product was noted when primers for X. index were tested with L. elongatus. Furthermore, when challenged with a range of non-target nematode species comprising the nematode community typical of viticulture soil, no PCR product was amplified. An experimental dilution series of extracted DNA rigorously demonstrated that DNA from an equivalent single specimen of the target virus-vector species, X. diversicaudatum and/or X. index, could be detected amongst 1000 equivalent non-targetX. vuittenezi. Also, extracted DNA from an equivalent single target specimen was detected when added to DNA extracted from the overall soil nematode community. The primers were assessed further by using serial mixtures of actual nematodes rather than extracted DNA to simulate field soil. Using this method, a single target nematode could be detected amongst 200 non-target specimens. Given their specificity, sensitivity and reliability, it appears that these diagnostic primers will be of great benefit to phytosanitary/quarantine services related to the viticulture industry.