新疆北部森林生态系统地衣植物生活型分析

Life forms of lichen of forest ecosystem in Northern Xinjiang were researched in the Kanas National Natural Reservation Area.They have been grouped into 6 types:Epipetria,Soil-epipetria,Epiphytia arboricosa,Epiphytia moss,Epiphytis grass and Dry-radicantia,in which the species of Epiphytia arboricosa account for 36.89% of the total species in this area,the species of Epipetria for 22.33% and Epiphytia grass the least.The results show that life forms of lichem at the srea in Northem Xinjiang are relatively rich,which indicates the biodiversity characteristics of lichen.     

DEVELOPMENT AND EVALUATION OF A RAPID ENZYME-LINKED IMMUNOFILTRATION ASSAY (ELIFA) AND AN ENZYME-LINKED IMMUNOSORBENT ASSAY (ELISA) FOR THE DETECTION OF STAPHYLOCOCCAL ENTEROTOXIN B

An enzyme-linked immunofiltration assay (ELIFA) and a microtitre plate enzyme-linked immunosorbent assay (ELISA) were developed and compared for their ability to detect staphylococcal enterotoxin B (SEB). The double antibody capture format was used for both assays. Factors which improved the sensitivity of the ELIFA system were (1) addition of casein and thimerosal to the antigen dilution buffer; (2) addition of polyethylene glycol (MW 6000) to the detection and conjugate antibody dilution buffers; and (3) washing with diethanolamine buffer prior to addition of the substrate/chromogen. The ELIFA system had a turnaround time of approximately 1 h and a detection limit of 1 ng/mL of purified SEB. The ELISA had a total turnaround time of 21 h, or 3 h using plates pre-coated overnight with the capture antibody. The detection limit of the ELISA for purified SEB was 0.05 ng/mL. The detection limit of SEB in cheese samples spiked with purified enterotoxin and subjected to a simple extraction procedure was 1 ng/mL and 0.1 ng/mL of extract, with the ELIFA and the ELISA, respectively.     

Physiological studies of a hybrid between populations of Dactylis glomerata from contrasting climatic regions. I. Inter population differences

A study of the physiological responses of a hybrid between a North European population and a colchicine-induced autotetraploid of a Portuguese population of Dactylis glomerata subspecies lusitanica showed an intermediate response of the hybrid for many characters. However, the hybrid resembled one or other of the parents in the more favourable expression of certain characters in controlled environments at 20°C, 16 h photoperiod and 8 °C, 8 h photoperiod. Rate of dry-matter production of the hybrid did not differ significantly from that of the northern parent at 20 °C, 16 h and that of the Portuguese parent at 8 °C, 8 h. Leaf growth of the hybrid at 8 °C, 8 h was greater than that of the northern parent and together with the high percentage survival in a freezing test may indicate a role for similar hybrids in the development of potential varieties with improved seasonal distribution of dry-matter production.     

Physiological studies of a hybrid between populations of Dactylis glomerata from contrasting climatic regions. II. Intra population variation

Mushroom compost was treated with nematicides and infested with Aphelenchoides composticola at the time of filling into growing containers. Yields of mushrooms from infested untreated control composts were reduced to 40–60% of yields from uninfested control compost. Yields from infested compost treated with fenamiphos emulsifiable concentrate (e.c.) at 10 or 20 mg a.i./kg, thiabendazole wettable powder at 40 or 60 mg a.i./kg or oxamyl granules at 20 mg a.i./kg were as high as from uninfested controls. Compost treated with granules of AC 64,475 up to 20 mg a.i./kg or ethoprophos or thionazin up to 80 mg a.i./kg gave yields significantly lower than uninfested controls. Numbers of nematodes rose to about 10⁶/20 g of compost in untreated compost and then fell, and a similar peak occurred in treatments in which yields were substantially reduced by nematode damage. Treatments which yielded as well as the uninfested controls held maximum nematode numbers down to about 10V20 g of compost but populations stayed at this level or tended to rise while numbers in untreated compost fell. Incorporation of fenamiphos in casing or its application to the surface of beds 3 wk after cropping began gave lower yields than the uninfested control but mushrooms were being produced late in the cropping cycle. Fenamiphos e.c. at 20 mg ai./kg incorporated in compost is considered a practical preventive measure for control of A. composticola.     

新疆天山西部山脉森林生态系统地衣群落结构的初步研究

 根据多年的研究资料并采用聚类分析方法对分布在天山西部山脉的地衣群落结构进行了研究。结果表明,分布在该地区的地衣种类形成了6种群落:1) 土星猫耳衣（Leptogium saturninum)＋矮石蕊(Cladonia humilis)＋兰灰蜈蚣衣（Physcia caesia）群落;2）黑穗石蕊（Cladonia amaurocr     

FOCUSED DIFFERENCE TESTING FOR THE ASSESSMENT OF DIFFERENCES BETWEEN ORANGE JUICES MADE FROM ORANGE CONCENTRATE

Focused difference testing was applied to two orange juices prepared from frozen concentrate. Differences were noted between the juices for darkness of color, visual appearance of pulpiness, resistance to tongue movement, flavor by mouth, odor, overall taste and taste other than sweetness. The logic and approach of focused difference testing is discussed and contrasted with other sensory analytical techniques.     

蓝麻黄的组织培养和快速繁殖

1植物名称蓝麻黄(Ephedra glaoca). 2材料类别2000年11月下旬,从新疆托克逊县科委蓝麻黄人工种植实验地取蓝麻黄,连土移栽到大花盆中,放到温室中培养,以其新生幼枝条为外植体. 3培养条件(1)诱导愈伤组织培养基:MS NAA1.5 mg·L-1(单位下同);(2)愈伤组织继代培养基:MS KT 0.05 2,4-D 1.0;(3)诱导芽分化培养基:MS 6-BA 3 IAA 0.2;(4)诱导腋芽培养基:MS 6-BA 0.4.以上培养基均附加3%蔗糖、0.7%琼脂,pH 5.6～5.8.培养温度24～26℃,光照时间15 h·d-1,光照度2 000～3 000 lx.     

禽多杀性巴氏杆菌P1059成熟黏附蛋白的原核表达、纯化和抗原性检测

目的：建立rCPM36在大肠杆菌中的表达体系,纯化表达产物并检测其抗原性。方法：运用PCR方法从禽多杀性巴氏杆菌国际标准株P1059基因组中扩增出编码36kDa成熟黏附蛋白的cpm36基因,构建原核表达载体pQE30-cpm36,转化到大肠杆菌M15中并诱导表达目的蛋白,用镍离子螯合层析柱纯化目的蛋白及制备其抗体,Western印迹分析其抗原性。结果：SDS-PAGE结果显示目标蛋白以可溶性形式表达在大肠杆菌M15细胞质中,其相对分子质量为37kDa,Western印迹结果表明表达蛋白具有良好的抗原性。结论：成功构建出原核表达载体并实现了目的蛋白表达,用镍离子螯合层析柱纯化得到具有抗原性的蛋白,为进一步开展禽多杀性巴氏杆菌黏附因子和保护性抗原的研究奠定基础。     

Isolation and characterization of microsatellite loci in the sand fly Phlebotomus papatasi (Diptera: Psychodidae)

Phlebotomus papatasi is a proven vector of Leishmania major which is one of the causative agents of cutaneous leishmaniasis in the Old World. Although it has a wide geographical range, its population structure is not yet well understood. In an effort to better understand the population dynamics of this vector, we developed a panel of di‐ and trinucleotide microsatellite markers, using a magnetic bead hybridization enrichment protocol. These microsatellite loci showed three to seven alleles with an expected heterozygosity range between 0.702 and 0.876. The level of polymorphisms found in this study suggests that these microsatellite loci can be used for population analysis of P. papatasi.