首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 46 毫秒
1.
安徽虫瘟霉菌株的强毒杀蚜应与侵染速率   总被引:5,自引:2,他引:3  
许谦  冯明光 《菌物系统》2000,19(2):241-247
报道安徽虫瘟霉(Zoophthora anhuiensis)菌株F97028对桃蚜(Myzus persicae)的强毒杀蚜活性。以7个孢子剂量(0.4 ̄10.4个孢子/mm^2)接种2 ̄3龄若蚜(52 ̄86头/剂量),连续观察7d,所获数据经时间-剂量-死亡率模型模拟分析,接种后第3 ̄7d的LD50分别为34.8、87、1.5、0.7和0.4个孢子/mm^2;在所有剂量范围内LT50为2.9 ̄6  相似文献   

2.
P物质对大鼠DRG神经元胞体膜的作用   总被引:17,自引:1,他引:17  
本文在大鼠DRG神经元标本上应用细胞内记录,以确定SP对DRG细胞的膜反应及其可能的离子机制。实验所测DRG细胞静息膜电位为-58.9±8.2mV(X±SE,n=81)。传导速度:A_(α/β)细胞为20.4±4.8m/s(X±SE),范围14.1-28.7m/s(47/60);Aδ及C类细胞为9.8±5.2m/s,范围1.2-13.7m/s(13/60)。浴槽滴加SP(10 ̄(-7)-3×10 ̄(-4)mol/L)在大多数细胞可引起明显的膜去极化反应(56/60)。少数细胞对SP无反应(4/60)。在SP去极化期间膜电导值有所增加,从平均值2.72×10 ̄(-8)mho增加24.6%(n=3)。所测逆转电位值在+40-+50mV之间(n=3)。浊流平衡液(BSS)中NaCl以氯化胆碱置代,或用含TTX(10 ̄(-5)mol/L)的BSS灌流,可使SP-去极化幅值大大减小但不能完全消除。而高(20mmol/L)和低(0mmol/L)Ca ̄(2+)的BSS灌流时,使SP-去极化幅值相应的增加和降低。用含10 ̄(-4)mol/LCd ̄(2+)及10 ̄(-2)mol/LTEA的BSS灌流,均使SP-去极化明显减小。  相似文献   

3.
山西运城盐池湖区裸藻植物及其分布特点   总被引:2,自引:0,他引:2  
在山西运城盐池湖区采到的裸藻门植物共10属83种(包括变种和变型),其中,绿色裸藻类77种,无色裸藻类6种。该区域的水体根据其含盐量的不同可分为4种类型:淡水水体(含盐量0.001-0.05%)、混盐水体(含盐量0.05 ̄3%)、真盐水体(含盐量3-4%)和高盐水体(含盐量4-34.7%)。由于含盐量不同的影响,裸藻门植物在4种水体中的分布有明显差异,总的趋势是裸藻门植物的种数随着含盐量的增加而减  相似文献   

4.
本文研究了Lys381变为Ala的精氨酰-tRNA合成酶(ArgRS)变种ArgRS381KA的最适pH和稳态动力学性质;比较了此酶与天然酶ArgRS的荧光光谱性质和热稳定性。实验结果表明ArgRS381KA的氨酰化活力和ATP ̄PPi交换活力的最适pH分别为8.0和7.0,与天然酶相同;ArgRS381KA的氨酰化活力对精氨酸、ATP和tRNAArg的Km分别为12μmol/L、0.3mmol/L和1.1μmol/L,Vmax为16000U/mg,kcat为16s-1;ATP ̄PPi交换活力对精氨酸、ATP和PPi的Km分别为92.9μmol/L、0.85mmol/L和80.1μmol/L,Vmax为28000~30000U/mg,kcat为32s-1.ArgRS381KA的荧光激发光谱和发射光谱与ArgRS基本相同。热失活速度比天然酶慢。  相似文献   

5.
目的 探讨将维生素A缺乏(VAD)胎鼠作为先天性心脏病动物模型的可行性。方法取11-19d不同胎龄正常及VAD胎鼠心脏经石蜡包埋、切片及 HE染色观察其发育情况。结果 1.实验组饲料含维生素A(VA)7μg/100g,经VAD饮食喂养后实验组大鼠血清VA水平明显低于对照组[(0.168±0.059)μmol/L Vs(2.18±0.23)μmol/L,t=32.88, P<0.001]。 2.大鼠死亡百分比:饲养于屏障系统的VAD大鼠死亡百分比较饲养于开放系统中的要低4.6倍(10% Vs 45.83%.x 2=16.64, P<0.001),对照组为0。 3.实验组大鼠受孕百分比及每只孕鼠产仔数均低于对照组[58.33% Vs 81.5%, x 2=4.37,P<0.05:(6.97±2.79) Vs(13 ±1.05),t=7.16, P<0.001]。 4.经切片观察11~15 d胎龄胎鼠实验组心脏出现明显发育延迟的占36.67%, 16~19 d胎龄胎鼠实验组心脏畸形占41.43%,血管异常占18.57%。结论VAD胎鼠可用来作为先天性心脏病动物模型,但需改进饲养环境以减少异常死亡。  相似文献   

6.
安徽沱湖夏季浮游植物群落结构特征与环境因子关系   总被引:3,自引:0,他引:3  
为了揭示沱湖浮游植物群落结构特征及其与水环境因子的关系,于2016年7月(夏季),对沱湖流域上游至下游11个采样点浮游植物种类组成、细胞丰度、生物量等进行调查研究。结果显示,沱湖共有浮游植物96种(含变种),隶属8门48属,其中绿藻门(Chlorophyta)和硅藻门(Bacillariophyta)种类最多,绿藻门有23属39种,占总种数的40.63%,硅藻门有7属20种,占总种数的20.83%;其次为裸藻门(Euglenophyta),有5属17种,占总种数的17.71%,蓝藻门(Cyanophyta) 8属14种,占14.58%;甲藻门(Pyrrophyta) 2属2种,隐藻门(Cryptophyta) 1属2种,各占总种数的2.08%,黄藻门(Xanthophyta)与金藻门(Chrysophyta)均有1属1种,均占总种数的1.04%。绿藻和硅藻类物种在沱湖浮游植物群落结构中处于优势地位,沱湖夏季浮游植物种类组成表现为绿藻-硅藻型。沱湖夏季浮游植物细胞丰度与生物量从上游到下游呈逐渐增加趋势,细胞丰度与生物量平均值分别为4.022×106cells/L与3.046 mg/L,蓝藻门和绿藻门类群为沱湖浮游植物细胞丰度主体,硅藻门和裸藻门类群为沱湖浮游植物生物量的主体;上游浮游植物多样性指数与均匀度指数均略高于下游采样点,沱湖水质呈β中污型-无污染型,上游水质优于下游水质。浮游植物群落结构与水环境因子的典型对应分析(CCA)结果表明,电导率、透明度、水深及pH值等环境因子与沱湖夏季浮游植物群落结构有较强的相关性。  相似文献   

7.
杭州西湖初步治理后的浮游植物现状   总被引:10,自引:0,他引:10  
本文记录了杭州西湖初步治理后的浮游植物种类组成、相似性、数量分布与环境理化因子的关系,以及根据指示种类评价了西湖水质。在1985年2月至1986年2月周年调查的20个站位中,共鉴定了浮游植物7门92属229种、变种和变型;其中蓝藻门19属39种;绿藻门35属87种8变种1变型;硅藻门24属54种7变种1变型等。西湖浮游植物的数量分布以外湖最高,年均值为529.1×105个/L,三潭内湖最低,仅1.76×105个/L。全湖每升水样含浮游植物细胞密度年均值为614×105个,并且以蓝藻占绝对优势,年均值为423×105个/L,绿藻、硅藻次之,分别为97.3×105个/L和77×105个/L。不同站位浮游植物种类组成的相似性指数值(sorensen 公式)在51.3-85.3范围。    相似文献   

8.
报道了缢蛏碱性磷酸酶(简称ALP)经不同浓度盐酸胍处理时酶的分子构象所发生的变化以及酶变化和失活的动力学过程。在胍中酶荧光发射峰强度下降,紫外差光谱在246nm和285nm处出现2个负峰,CD谱中酶的α螺旋度下降,且随浓度增大,变化程度也加大。动力学研究表明,酶在0.5mol/L、1.0mol/L、2.0mol/L3.0mol/L、4.0mol/L盐酸胍中的变性速度常数分别为3.21×10~(-4)s~(-1)、6.38×10~(-4)s~(-1)、2.17×10~(-3)s~(-1)、2.33×10~(-3)s~9-1)、5.17×10~(-3)s~(-1);而酶在相应盐酸胍中的失活速度常数分别为2.33×10~(-4)s~(-1)、3.57×10~(-4)s~(-1)、5.86×10~(-4)s~(-1)、1.14×10~(-3)s~(-1)、3.45×10~(-3)s~(-1);表现为失活与构象伸展变化基本平行。  相似文献   

9.
虫壳属一新种大别山虫壳(Torrubieladabieshanensis)及其同时在蛛体上并存的无性型大别山球束梗孢(Gibeluladabieshanensis)。子囊壳表生至浅埋生,孔口黄色,子囊孢子弹射后呈波浪形弯曲。次生子囊孢子长柱形,9.4~15.1×0.7~1.2μm。孢梗束单个或两个,白色,在其2/3处仍有分生孢子梗。分生孢子梗长27~44μm,光滑。分生孢子纺锤形,3.2~4.0×1.1~1.8μm。具糙梗孢式的共无性型方式,分生孢子线形,11.0~20.0×0.7~1.1μm。列出了该属已知种的检索表,并分别命以中名  相似文献   

10.
以0.1mol/LNH4Cl溶液为介质,用2.5次微分伏安法测定了丙二醛,线性范围为1.0*10^-6至1.0*10^-3mol/L,检测限达1.0*10^-7mol/L。并测定了细胞培养液介质中新生SD大鼠室肌细胞样品的丙二醛。  相似文献   

11.
12.
13.
It has now been over twenty years since a novel herpesviral genome was identified in Kaposi's sarcoma biopsies. Since then, the cumulative research effort by molecular biologists, virologists, clinicians, and epidemiologists alike has led to the extensive characterization of this tumor virus, Kaposi's sarcoma-associated herpesvirus(KSHV; also known as human herpesvirus 8(HHV-8)), and its associated diseases. Here we review the current knowledge of KSHV biology and pathogenesis, with a particular emphasis on new and exciting advances in the field of epigenetics. We also discuss the development and practicality of various cell culture and animal model systems to study KSHV replication and pathogenesis.  相似文献   

14.
15.
16.
17.
Comprises species occurring mostly in subtidal habitats in tropical, subtropical and warm-temperate areas of the world. An analysis of the type species, V. spiralis (Sonder) Lamouroux ex J. Agardh, a species from Australia, establishes basic characters for distinguishing species in the genus. These characters are (1) branching patterns of thalli, (2) flat blades that may be spiralled on their axis, (3) width of the blade, (4) primary or secondary derivation of sterile and fertile branchlets and (5) position of sterile and fertile branchlets on the thalli. Application of the latter two characters provides an important basic method for separation of species into three major groups. Osmundaria , a genus known only in southern Australia, was studied in relation to Vidalia , and its separation from the Vidalia assemblage is not accepted. Species of Vidalia therefore are transferred to the older genus name, Osmundaria. Two new species, Osmundaria papenfussii and Osmundaria oliveae are described from Natal. Confusion in the usage of the epithet, Vidalia fimbriala Brown ex Turner has been clarified, and Vidalia gregaria Falkenberg, described as an epiphyte on Osmundaria pro/ifera Lamouroux, is revealed to be young branches of the host, Osmundaria prolifera.  相似文献   

18.
Fifteen chromosome counts of six Artemisia taxa and one species of each of the genera Brachanthemum, Hippolytia, Kaschgaria, Lepidolopsis and Turaniphytum are reported from Kazakhstan. Three of them are new reports, two are not consistent with previous counts and the remainder are confirmations of very scarce (one to four) earlier records. All the populations studied have the same basic chromosome number, x = 9, with ploidy levels ranging from 2x to 6x. Some correlations between ploidy level, morphological characters and distribution are noted.  相似文献   

19.
肝癌中HBV和HCV基因和抗原的分布及意义   总被引:1,自引:0,他引:1  
采用原位分子杂交方法检测HCV RNA及HBV X基因;采用免疫组织化学方法研究HCV核心抗原,非结构区C33c抗原及HBxAg在肝细胞肝癌中的定位及分布.结果表明(1)HCV RNA、HBV X基因在肝细胞肝癌组织检出率分别为40%(55/136)和82%(112/136).HCV RNA定位于癌细胞的胞浆内,阳性细胞呈散在、灶状及弥漫分布三种形式;HBV X基因在肝癌细胞中的分布呈胞浆型、核型及核浆型,阳性细胞也呈上述三种分布形式;(2)HCV C33c抗原、核心抗原在肝细胞肝癌中的阳性率为81%(133/164)及86%(141/164).C33c抗原定位于癌细胞及肝细胞的胞浆内;核心抗原既定位于癌细胞核中,又可定位于胞浆中.C33c抗原阳性细胞以灶状分布为主;而核心抗原阳性细  相似文献   

20.
For a plant selection model with frequency-independent viabilities, fertilities and selfing rates, it is shown that apart from global fixation, for certain parameter combinations a protected polymorphism and facultative fixation (either allele may become fixed according to initial frequencies) may both occur. Facultative fixation requires different selling rates for the dominant and recessive type. Protection of the polymorphism requires resource allocation for male and female function. In this connection the problem of purely genetically caused population extinction is discussed.
For general frequency dependence and regular segregation, the chances for establishment of a completely recessive gene are compared to those of a completely dominant gene. It is proven that the process of establishment of the recessive gene, despite a fitness advantage, may be considerably endangered by drift effects if random mating prevails. The recessive gene may reach the same effectivity in establishment as a dominant gene, only if the recessive homozygote mates exclusively with its own type during the period of establishment.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号