苹果试管苗不定根起源及其发育状况的研究

利用光学和扫描电子显微镜观察结果表明,经琼脂生根培养基诱导产生的长富—2苹果 (Malus pumila Mill.) 试管苗的不定根起源于维管形成层。这种不定根发育不良,根表面缺乏根毛,内部解剖构造为典型的初生结构。为避免因不定根吸收、运输能力差而影响试管苗移栽成活,宜采用通透性良好的基质进行瓶内或瓶外生根,可诱导出优质不定根。     

森林可燃物的燃烧性与化学组成

从五种针叶树叶(白皮云杉、红松、兴安落叶松、黑皮油松、樟子松)以及六种阔叶树叶(柳树、白桦、杨树、黄波罗、水曲柳、蒙古栎)的春季和秋季样品的水分、灰分(水溶性和水不溶性)、醚抽提物、含氮量、含磷量的分析得出:兴安落叶松和柳树的可燃性最小。这一结果与热重分析所得结果相符合。     

肾俞穴,后三里穴与子宫相关的神经基础

应用辣根过氧化物酶（ＨＲＰ）法和荧光素双标记法，研究了家兔子宫与肾俞穴、后三里穴的外周神经联系。结果显示，支配子宫与肾俞穴、后三里穴的初级传入神经元及交感节后神经元分布节段部分重叠，在腰１（Ｌ１）脊神经节有少量的荧光素双标记细胞，约占该节荧光素标记细胞总数的２．６％，表明Ｌ１脊神经节有一些初级传入神经元，其周围突分支分布于肾俞穴和子宫，提示子宫与肾俞穴除通过中枢途径联系外，还可通过外周突分支投射的感觉神经元直接相联系；在胸１２～荐３（Ｔ１２～Ｓ３）交感神经节出现大量分别支配子宫和后三里穴的标记细胞，这两种细胞紧密相邻，提示支配子宫和后三里穴的交感节后神经元之间，可能还存在直接或间接联系。上述结果为穴位－内脏相关机理提供了形态学证据。     

南方鲶肌肉,鳔及胡子鲶肌肉的水解和游离氨基酸研究

本试验测定了南方鲶肌内和鳔及胡子鲶肌肉的水解氨基酸和游离氨基酸含量，并对其营养价值进行了比较，评价。     

越桔对长白山区酸性土壤的适应性

在长白山区３种类型的酸性土壤上栽培越桔，研究结果表明，｀北空＇、｀美登＇、｀斯卫克＇在暗棕色森林土上生长结果较好，树体营养关系合理；在草甸沼泽土上３个种生长结果均较差，｀北空＇在水湿地潜育土上生长旺盛，但产量低，综合分析认为，矮丛越桔类型品种对我国长白山区酸性土壤条件的适应性较强，半高丛越桔则适应性差，针对长白山不同类型的土壤，以美登最为适宜暗棕色森林土栽培，斯卫克次之；水湿地潜育土可栽培美登品种     

蓝舌病灭活疫苗免疫羊ELISA和琼扩监测比较试验

用19只绵羊（注苗前BTV琼扩和ELISA均为阴性）注射BTV灭活苗后7～139天的血清进行BTVELISA和琼扩平行试验，结果表明，注苗后7～30天11只试验丰ELISA阳性，注苗40天13只羊ELISA阳性，注苗90天以后全部试验羊只均为ELISA阳性，而琼扩试验则始终为阴性结果。     

金定鸭的性双态分化和性行为发育

金定鸭的外型分化，受自然选择和性选择的双重影响。在生长发育过程中，依羽域在适应水域环境的重要性，雌雄金定鸭的正羽都按共同的羽域顺序陆续更换生长；与此同时，一日龄外型相同的异性雏鸭，逐渐表现出性双态，包括喙色、羽色、声音、性羽、体重和行为的表型差异，以满足繁殖竞争的需要。金定鸭性行为的出现以其性双态分化为基础，而性行为的分化又是其生理成熟的前提条件。对雄鸭的观察分析结果表明，性双态分化和性行为发育速度的快慢与其生理成熟的早迟是一致的。黑色尾羽的雄鸭，体重较小，其发育速度和性成熟均快于体重较大的白喙或端白尾羽者，因此，建议将尾羽颜色、性双态分化和性行为发育速度作为雄鸭的选育指标。     

Analysis and pharmacokinetics of cimaterol in growing Holstein steers.

Pharmacokinetic parameters for the beta 2-adrenergic agonist, cimaterol (CIM), were determined in growing Holstein steers. Compartmental analysis was used after measurement of CIM in body fluids by affinity chromatography and HPLC using UV detection. Recoveries from spiked plasma and urine standards were 70 +/- 1.2% and 68 +/- 1.1%, respectively. The minimum detection level in plasma was 1 ng/mL and the average CV was 5.1% for concentrations that ranged from 1 to 30 ng/mL. Four steers (276 +/- 24 kg) received 15 mg of CIM by bolus intravenous injection. Plasma CIM levels declined in a biphasic manner with half-lives of 2.5 min for the distribution phase and 54 min for the elimination phase. A two-compartment open model was used to describe the disappearance of CIM and the following pharmacokinetic parameters were obtained: central compartment volume (Vc) = .76 L/kg, apparent volume of distribution (Vd) = 4.1 L/kg, and transfer rate constants from the central to peripheral compartment (k12) = .177/min, from the peripheral to central compartment (k21) = .054/min and elimination from the central compartment (kel) = .074/min. After 8 h, total urinary CIM accounted for only 18.3% of the administered dose. Results suggest that circulating concentrations of CIM in growing steers are influenced by its accumulation in an unidentified peripheral pool and its conversion into unknown metabolite(s) before elimination.     

Eastern equine encephalitis in a flock of emus (Dromaius novaehollandiae).

Eastern equine encephalitis (EEE) was diagnosed in a flock of emus in southeastern Louisiana. The outbreak involved juvenile and adult breeders ranging in age from 20 to 36 months, with an attack rate of 76% and a case fatality rate of 87%. The diagnosis was confirmed by isolation and characterization of the viral agent, and by detection of EEE antibody in two recovered emus. High mortality was preceded by marked depression, hemorrhagic diarrhea, and emesis of blood-stained ingesta. On postmortem examination, hemorrhagic enteritis and multiple petechia of viscera were observed. Microscopic changes included severe necrosis of hepatocytes, intestinal mucosa, and necrotizing vasculitis of the spleen and lamina propria of the intestine. No nervous system lesions were observed. This outbreak occurred concurrently with EEE in horses and was attributed to unseasonably heavy rainfall with an abundance of arthropod vectors and proximity to free-living reservoir host species.     

单克隆抗体ELISA检测犊牛粪便中冠状病毒抗原

用两株单克隆抗体混合后包被ＥＬＬＩＳＡ微孔板，加牛冠状病毒抗原，加经白陶土处理过的兔抗牛冠状病毒免血清，再加上辣根氧化物酶标记的羊抗兔ＩｇＧ抗体，加底物质显色间接ＥＬＩＳＡ检测牛冠状病毒抗原获得成功。用此方法检测细胞培养的牛冠状病毒上清液，其敏感度高出血凝试验（ＨＡ）８倍，从武汉市附近３个奶牛场采集犊牛腹泻粪便１０５份，用单抗ＥＬＩＳＡ检测牛冠状病毒抗原，共检出阳性３６份，并与血凝及血凝抑制试验，