长春市主要广场城市森林结构的研究

通过样地调查对长春市主要广场的城市森林结构进行分析得出：广场森林的密度为160株／hm^2，广场共有乔木树种52种，花灌木30种。树木的平均胸径为21．6cm，树木的总叶面积为739172．8m^2，叶面积指数为1．2，广场森林总生物量为5174．2t，Shannon-Wiener指数平均为1．7。从以上分析可以看出长春市主要广场园林植物种类丰富，并已达到森林水平可以发挥出很大生态效益。     

高层建筑外部空间的形态构成

对城市建筑环境中高层建筑外部空间的形态构成进行了分析,并从外部空间的类型、外部空间的尺度感、外部空间的闭合与开放、外部空间的环境层次四个方面对其进行了详细论述。     

青海城镇体系发展的历史轨迹与动力

青海城镇体系经历了发韧期、奠基期、转型期3个发展历程.在这一过程中,湟水谷地最先拉开了城镇发展的历史帏幕,随后逐步向西扩展进入青海湖地区.宏观上,从农耕区向农牧交错区渗透,进而向游牧区拓展,反映了社会历史进程和地域开发进程的调控作用,因此城镇分布数量和密度呈现出农耕区—农牧交错区—游牧区逐级递减的趋势.中观上,以河流为脉络,城镇发展或溯源而上伸入高原腹地,或向河谷两岸推进,进入山区,表现为从优势生存空间向劣势生存空间的时空转化,城镇数量与密度呈现出川水地区—浅山地区—脑山地区的递减趋势.微观上,河谷农耕区城镇选址多位于河流阶地上,土地肥沃,取水便利;而牧区城镇的选址却往往与水草丰美的牧场相关,映射出古代城镇对自然条件和自然物质基础的依赖性.总体而言,青海省城镇兴起和发展的动力,主要来自于外部中央行政建制和军事据点的设置,而非城镇内部社会经济自我发展.就单个城镇而言,民族文化、民族宗教与民族贸易的亲合关系和响应力,是城镇成长的主要推进剂.     

A new indolic antiauxin, α-(5,7-dichloroindole-3-)isobutyric acid: its chemical synthesis and biological activity

Summary A new potent antiauxin, -(5,7-dichloroindole-3-)isobutyric acid has been synthesized and shown to inhibit auxin-mediated elongation ofAvena coleoptiles and to stimulate root growth of rice seedlings. Its activity is stronger than -(p-chlorophenoxy)isobutyric acid and is comparable to that of 2,3,5-triiodobenzoic acid, which are typical antiauxins.     

城市化途径及其相关

对城市化途径有关各要素作了综合的叙述,并且指出研究的手段──自人口的聚集至城镇形成发展这一历史的纵剖面及地域、产业结构等横向有关要素作整体系统的分析与比较,并指出应重点研究人口指标分析、产业可比关系、城市化和城市化设施,以及城市体系的研究问题。     

华佗再造丸治疗脑血管病疗效评估

用华佗再造丸治疗脑血栓、脑出血及其后遗症52例,其有效率达90.5％,对照组20例,10例脑出血用20％Mannitol及止血剂治疗,10例脑血栓用低分子右旋糖酐及脑络通治疗,有效率为70％,有高度显著性差异,P<0.001,笔者认为该药是治疗脑血管病较理想的中成药,具有镇静神经,滋阴强心,舒经活络,活血化瘀等作用。对病程短的年纪青的病人的疗效更为显著,脑出血性与脑缺血性疾病均有疗效,正是中药一药多用、一药多治的微妙体现。推测对脑血管病后遗症有效可能与该药能促进神经再生因子(NGF)的合成和利用有关。     

Proopiomelanocortin expression in the skin during induced hair growth in mice

We demonstrate for the first time a hair cycle-dependent gene and protein expression of proopiomelanocortin in mouse skin in vivo. Northern blot detected POMC mRNA with an apparent size of 0.9 kb in anagen but not telogen skin. Western blot emphasized a specific protein of 30–33 kDa recognized by anti -endorphin in late but not early anagen or telogen skin. By immunocytochemistry, -endorphin antigen was localized in the sebaceous gland in a hair cycle dependent manner.     

Purification of platelet-derived endothelial cell growth inhibitor and its characterization as transforming growth factor-β type 1

In 1986, Brown and Clemmons (Proc. natl Acad. Sci. USA83 (1986) 3321) showed that platelets contain a substance, platelet-derived growth inhibitor (PDGI), that inhibits in vitro endothelial cell replication. Although platelets are rich in transforming grwoth factor (TGF-), PDGI was considered not to be related to TGF-, on the basis of its reported properties (extraction from platelets at neutral pH, binding to heparin-Sepharose). However, we purified PDGI to near homogeneity and showed that on the basis of HPLC retention behavior, in vitro growth inhibitory activities with several cell types, receptor binding, and immunoneutralization of growth inhibitory activity with specific anti-TGF- type 1 antibodies, PDGI is most probably identical with TGF- type 1.     

In vitro mutagenicity testing of a potent,new, benzoyl urea insect growth regulator

Summary Bacterial mutagenicity assay to detect potential chronic toxicity of a potent, new, benzoyl urea insect growth regulator (CGA-112913 or IKI-7899, formerly UC-62644) was conducted using 5 histidine auxotrophs ofSalmonella typhimurium. Tests within the concentration range of 0.9–500 g (saturating)/plate of the compound with and without the 5–9 mammalian metabolic activation system showed no mutagenic effects clearing the way for long-term chronic toxicology studies.The authors thank Professor Bruce N. Ames for supplying the tester strains together with all the relevant information for conducting the bioassays and Ms. Norma Charlebois for her meticulous technical assistance.     

An enzyme immunoassay for mouse epidermal growth factor utilizing a liquid phase double-antibody system

Summary An enzyme immunoassay for mouse epidermal growth factor (EGF) involving a liquid phase double-antibody system was developed. The EGF--galactosidase conjugate prepared was stable for at least 8 months. By this method, EGF was detectable at a concentration as low as 20 pg per tube. The concentrations of EGF in various tissues of mice are also presented.This work was supported in part by a Grant-in-Aid for Scientific Research from the Ministry of Education, Science and Culture of Japan.