薇甘菊萎蔫病毒感染对薇甘菊光合特性和4种酶活性的影响

为明确薇甘菊萎蔫病毒(Mikania micrantha wilt virus,MMWV)对薇甘菊(Mikania micrantha)叶片生理生化的影响,探讨了MMWV侵染对薇甘菊叶片超氧化物岐化酶(superoxide dismutase,SOD)、过氧化物酶(peroxidase,POD)、多酚氧化酶(polyphenol oxidase,PPO)和苯丙氨酸解氨酶(phenylalanine ammonia-lyase,PAL)活性及叶绿素总含量和光合特性的影响.结果表明:MMWV感染薇甘菊16d内叶片的SOD活性均比对照组高,其中第16天达最大值,但接种后第24和32天SOD活性分别比对照低了13.28％和25.37％;POD活性在接种后16-32d均显著高于对照.PPO和PAL变化趋势相似,在接种后第8天这两个酶的活性分别比对照高了77.75％和23.58％,而在第32天分别比对照减少了14.27％和20.53％.随着侵染时间的增加,感病薇甘菊叶片中叶绿素含量减少,叶绿素a/b值逐步降低;同时最大净光合速率(Pmax)和光饱和点(LSP)分别比健康对照减少了32.34％和12.52％,而对暗呼吸速率(Rd),光补偿点(LCP)和表观量子效率(AQY)无显著影响.表明MMWV侵染可减低薇甘菊叶片光合作用的效率.     

紫云英与双季稻秸秆协同利用影响稻田土壤钾循环与平衡

稻草还田和冬种绿肥是维持稻田地力和化肥替代的重要方式之一.本研究以在湖南酸性红黄泥和碱性紫潮泥两种典型稻田土壤上进行了2年的紫云英-双季稻定位试验为对象,分析紫云英和双季稻秸秆协同利用对稻田土壤K循环的影响.两土壤试验处理一致,包括稻田冬闲(FRR)、冬种紫云英(MvRR)及冬种紫云英与水稻秸秆协同利用(MvRR+St...     

南方红豆杉扦插繁殖技术研究

2003~2004年应用2年生南方红豆杉幼苗进行扦插试验研究,结果表明:不同时间扦插的插穗生根时间最多相差2个月,2月中旬至3月中旬为最适宜扦插季节,扦插后3~5个月的生根率高于其它月份。用河沙与红泥作基质扦插,在不同季节扦插中以河沙作基质的生根效果比红泥的好。用生根剂处理有利于插穗提早生根及增加生根数量,以冬季及早春应用的效果较为明显,应用生根剂的插穗在扦插3~5个月后的生根率和生根数量与对照比有显著差异。不同类型插穗的扦插生根率在不同月份扦插的结果不同,但其差异不显著。     

Significance of salt transport patterns in rice varieties differing in salt tolerance

Abstract

The absorption mechanisms for Na, K, SO₄ and Cl were tested in a salt tolerant (PVR 1) and a salt sensitive (GEB 24) rice varieties. The salt tolerant variety accumulated significantly larger amounts of Na than the salt sensitive variety. Further, PVR 1 absorbed SO₄ from Na₂SO₄ in preference to that from K₂SO₄. The absorption patterns for K and Cl were similar in both the varieties. It is concluded that the capacity of plant species to accumulate greater amounts of Na is a reflection of their halophytic feature.     

不同氮磷钾配比对仙客来生长的影响

对仙客来无土栽培营养液中N、P、K元素采用三因素二次D-饱和最优设计,探讨不同浓度氮磷钾对仙客来生长发育的影响,对仙客来的根长、根体积、球茎直径、花朵数、花瓣长、可溶性糖含量、MDA含量、蛋白质含量、叶绿素含量进行分析。结果表明:经方差分析和主成分分析得出,无土栽培仙客来氮、磷、钾最优组合方案为:86.6~263.4、60~100和250~400 mg/L,即氮:磷:钾为3∶1∶6.5。     

Forest soil chemical changes following fire

Abstract

Prescribed fire to remove residue in a pine plantation on a sandy soil resulted in increases in pH, P, K and Ca in the top 20 cm of soil during the first 15 months following treatment.     

沙障固沙原理的研究

提出了不以粗糙度而以障内沙面蚀积强度作为沙衡量沙障固沙效能的综合标志，主张通过障埂占位，通过对障埂高度和障梗间距的调节控制风沙流的蚀积机制，在此基础上推导了控蚀公式，并以Ｋ值等于１／１０作为沙障成败优劣的判断标准，对指导治沙实践具有较强的可操作性。     

华东地区部分猪源大肠杆菌K88黏附素的生物学特性

近年来，从华东地区患腹泻仔猪中分离到一些表达K88菌毛的大肠杆菌，这些菌株只与K88a因子单抗反应，而不与b、c、d因子单抗反应。通过K88常规血清交叉吸收试验、SDS-PAGE、Western印迹，表明这些菌株不仅与K88ac参考菌株C83907制备的c因子血清反应，而且与以分离株SEC586制备且经K88ab、K88ac、K88ad参考菌株吸收后的血清也反应。对分离株SEC586、SEC464的K88主要亚单位结构基因faeG的克隆、测序，发现该基因由846对核苷酸组成，编码菌毛主要亚单位的262个氨基酸及21个氨基酸的信号肽，比国外报道的K88ac FaeG亚单位（263个氨基酸）少了1个氨基酸，比K88ab、K88ad（265个氨基酸）少了3个氨基酸。SEC586、SEC464菌株的FaeG亚单位氨基酸序列的同源性为97．7％，它们与K88ac的同源性为94．7％和96．2％；与K88ab的同源性为90．1％和91．2％；与K88ad的同源性为87．0％和88，6％。结果表明，新分离的K88ac大肠杆菌黏附素主要亚单位已发生了部分变异。     

Specificity of polycllonal and monoclonal antibodies for the identification of Xanthomonas campestris pv. campestris

Polyclonal and monoclonal antibodies (PCAs and MCAs), produced to whole cells and flagellar extracts ofXanthomonas campestris pv.campestris (Xcc), respectively, were tested for specificity. In immunofluorescence microscopy (IF) the three PCAs tested, reacted at low dilutions with all Xcc strains, some other xanthomonads and non-xanthomonads. At higher dilutions most cross-reactivity with non-xanthomonad strains disappeared. However, the cross-reactivity with strains ofX. c. pv.vesicatoria (Xcv),X. c. pv.amoraciae (Xca) andX. c. pv.phaseoli var. fuscans (Xcpf) remained.Six MCA-producing cell clones viz. 20H6, 2F4, 18G12, 10C5, 17C12 and 16B5 were selected for specificity tests with an enzyme immunoassay (EIA), IF and a dot-blot immunoassay (DBI). None of the MCAs reacted with all Xcc strains in IF and EIA. In DBI, only MCAs 17C12 and 16B5 reacted with all Xcc strains. All six MCAs tested, cross-reacted in one of either tests with other pathovars ofX. campestris, such as Xcv or Xca. The MCAs were also tested in immunoblotting experiments using total bacterial extracts, cell envelope and flagellar extracts. MCAs 20H6, 2F4, 18G12 and 10C5 reacted with the lipopolysaccharide (LPS) of Xcc. MCAs 16B5 and 17C12 reacted with a 39 kilodalton and a 29 kilodalton protein, respectively.It is concluded that the PCAs and MCAs discussed in this study may be used for routine identification and differentiation of (a group of) Xcc strains. The significance of the cross-reactions with other pathovars ofX. campestris needs to be determined by testing seed lots.     

Development of a monoclonal antibody-based co-agglutination test to detect enterotoxigenic Escherichia coli isolated from diarrheic neonatal calves

Escherichia coli (E. coli) strains were collected from young diarrheic calves in farms and field. Strains that expressed the K99 (F5) antigen were identified by agglutination tests using reference antibodies to K99 antigen and electron microscopy. The K99 antigen from a selected field strain (SAR-14) was heat-extracted and fractionated on a Sepharose CL-4B column. Further purification was carried out by sodium deoxycholate treatment and/or ion-exchange chromatography. Monoclonal antibodies to purified K99 antigen were produced by the hybridoma technique, and a specific clone, NEK99-5.6.12, was selected for propagation in tissue culture. The antibodies, thus obtained, were affinity-purified, characterized and coated onto Giemsa-stained Cowan-I strain of Staphylococcus aureus (S. aureus). The antibody-coated S. aureus were used in a co-agglutination test to detect K99+ E. coli isolated from feces of diarrheic calves. The specificity of the test was validated against reference monoclonal antibodies used in co-agglutination tests, as well as in ELISA. Specificity of the monoclonal antibodies was also tested against various Gram negative bacteria. The developed antibodies specifically detected purified K99 antigen in immunoblots, as well as K99+ E. coli in ELISA and co-agglutination tests. The co-agglutination test was specific and convenient for large-scale screening of K99+ E. coli isolates.