我国六种新蚤雄性阉割描记及关于单齿新蚤的商榷(蚤目：多毛蚤科)

在所收藏的蚤类标本中,查出新蚤属6种、亚种2,例雄性阉割畸形,其中阿巴盖新蚤Neopsylla abagaitui 3例,二卤新蚤N,btdentatiformis 9例,类新蚤N.Compar 1例,近代新蚤东方亚种N.Pleskei orientalis 4例,鞍新蚤N.Sellaris 7例,特新蚤指名亚种N.S,specialis 1例。 这些标本获自黑龙江,吉林、内蒙古,宁夏、甘肃、河北和云南。本文对畸形蚤形态进行了描述。分析关于单齿新蚤 Neopsylla monodcntattformis Huang ct Xic,1987的原始描述和形态特征图,认为其鼓名模式可能系二齿新蚤畸形标本,那么其种名将成为国际动物命名法规拒绝的名称。     

红羊新蚤的地理分布、宿主关系和鉴别特征的研究(蚤目：多毛蚤科)

自从红羊新蚤Neopsylla hopgyangensis Li,Bai & chen,1986从宁夏回族自治区的海原和贺兰山林区发现并报道(四川动物5(2)：1-3)以后,青海、甘肃和陕西均先后发现他们以往鉴定为二齿新蚤的大多数为红羊新蚤。本文报道红羊新蚤的地理分布、海拔、主要宿主及鉴别特征的应用。     

宁夏新蚤属一新种记述(蚤目:多毛蚤科)

1980年9月至1985年9月期间,先后自宁夏回族自治区海原县红羊乡的月亮山、马场和贺兰山林区从大林姬鼠(Apodemus peninsulae)、灰仓鼠(Cricetulus migratorius)和社鼠(Niviventer confucianus)体上采到新蚤属Neopsylla Wagner,1903一种跳蚤。经鉴定为一新种,即以其主要产地命名为红羊新蚤Neopsylla hongyangensis,新种。鉴别特征红羊新蚤新种属于多毛蚤种团(Setosa-group),并与二齿新蚤N.bidentat-iformis(Wagner,1893)接近。但以其♂第9腹板肘部腹面中央有一向后方伸出的瓶形腹小臂可立即与二齿新蚤相区别。另外,第9腹板后臂的一列刺鬃…     

黄鼠洞干蚤和宿主密度的年间动态关系

根据内蒙古自治区正镶白旗乌宁巴图苏木1981～1993年达乌尔黄鼠Citellus dauriCUS密度和洞干蚤指数监测资料进行分析,得到如下结果。共检洞干蚤9种,其中方形黄鼠蚤蒙古亚种Citellophilus tesquorum mongolicus (66.0%)为优势蚤种,光亮额蚤Frontopsylla lu-culenta(23.6%)为次优势蚤种,阿巴盖新蚤Neopsylla abagaitui和二齿新蚤N。Bidentatifor-mis为常见种,余为少见种。鼠密度与洞干蚤指数关系显著(PPP<0.05),关系为洞干蚤指数=0.2709+0.0504体蚤指数。洞干蚤和巢蚤指数的关系是显著的(P<0.07),关系为洞干蚤指数＝0.27652+0.00348巢蚤指数。三种蚤指数之间有如下近似 关系：巢蚤指数：体蚤指数：洞干蚤指数：100：10：1。     

锡林郭勒草原布氏田鼠体蚤和巢蚤数量动态及蚤类群落演替

1989～1998年对内蒙古阿巴嘎旗那仁宝力格苏木布氏田鼠Microtus brandti体蚤和巢蚤的数量进行了调查和分析,所得体蚤包括3科7属9种, 其中优势种有: 原双蚤田野亚种Amphipsylla primaris mitis占41.84%, 近代新蚤东方亚种Neopsylla pleskei orientalis占41.18%, 光亮额蚤Frontopsylla luculenta占13.18%。所得巢蚤包括2科6属9种, 其中优势种近代新蚤占74.94%; 光亮额蚤占10.04%, 原双蚤占8.20%, 宽圆纤蚤Rhadinopsylla rothschildi占6.44%, 是常见种。田鼠体的原双蚤、近代新蚤、光亮额蚤和体蚤指数间呈正相关(P<0.05)。田鼠巢的近代新蚤、光亮额蚤、宽圆纤蚤和巢蚤指数间正相关显著(P<0.01)。春季巢蚤指数∶春季体蚤指数≈5∶1, 秋季巢蚤指数∶秋季体蚤指数≈75∶1。近代新蚤既是体型蚤又是巢型蚤, 为田鼠的优势蚤种; 原双蚤数量占体蚤的 41.84%, 是体型蚤; 光亮额蚤为体蚤和巢蚤中的常见种。     

黄鼠巢和宿主密度的年间动态关系

根据内蒙古自治区正镶白旗乌宁巴图苏木1981～1993年达乌尔黄鼠Citellus dauricus密度和巢蚤指数监测资料进行分析,得到如下结果。共检巢蚤10种,其中方形黄鼠蚤蒙古亚种Citellophilus tesquorum mongolicus(45.4%)为优势蚤种,光亮额蚤Frontopsylla lucu lenta(25.0%)和阿巴盖新蚤Neopsylla abagaitui(21.3%)为次优势蚤种。二齿新蚤N.Bidentatiformis和角尖眼蚤Ophthalmopsylla praefecta为常见种,余为少见种。鼠密度与巢蚤指数 的关系不显著(p>0.10)、与巢染蚤率关系显著(p<0.05),不同年份的蚤类多样性和均匀性比较稳定。巢蚤和体蚤指数的关系是显著的(PP<0.005)。     

二毫新蚤的分类研究（蚤目：多毛蚤科）

本文报告二毫新蚤Neopsylla biseta一新亚种二毫新蚤碧江亚种N.biseta bijiangensis ssp.n.,首次记述二毫新蚤绒鼠亚种新组合N:biseta eleusina(Li,1980)comb.n.的雄性,并重新描述二毫新蚤指名亚种N.biseta biseta Li et Hsieh,1964的雌性。     

哈尔滨郊区人为鼠疫疫源地蚤类种群动态分析

1982～1999年对黑龙江省哈尔滨郊区人为鼠疫疫源地达乌尔黄鼠Spermophilus dauricus巢蚤、体蚤、洞干蚤指数和染蚤率进行了调查和分析。共获蚤9种,其中方形黄鼠蚤松江亚种Citellophius tesquorum sungaris是优势种(89.39%),其次为二齿新蚤Neopsylla bidentatiformis (10.37%)。3类蚤指数、染蚤率的均值差异均显著(P<0.01)。巢蚤与体蚤指数相关显著(P<0.05)。巢蚤指数∶体蚤指数∶洞干蚤指数≈650∶140∶1; 巢染蚤率∶体染蚤率∶洞干染蚤率≈165∶88∶1。     

长爪沙鼠寄生蚤指数和气象因子关系的研究

根据内蒙古自治区土默特平原1983～1985年长爪沙鼠 Meriones unguiculatus巢蚤、体蚤、洞干蚤指数和6项气象资料进行分析,得到如下结果。① 共获蚤11种, 其中秃病蚤蒙冀亚种Nosopsyllus laeviceps kuzenkovi(67.50%)是优势种, 二齿新蚤Neopsylla bidentatiformis(22.65%)为次优势种。② 3种蚤指数的均值差异显著(P<0.0001)。③ 体蚤与洞干蚤指数相关显著(P<0.05), 模型为(洞干蚤指数)=0.0049+0.0248(体蚤指数), 巢蚤与体蚤、巢蚤与洞干蚤指数的相关不显著(P>0.25)。④ 沙鼠密度与3种蚤指数的相关均不显著(P>0.10)。⑤ 在巢蚤中,月温度是影响巢秃病蚤唯一的气象因子(P<0.05)。⑥ 分别求出鼠体的秃病蚤和同形客蚤指名亚种Xenopsylla conformis conformis与气象因子的最优回归子集(P<0.003、P<0.05), 洞干的秃病蚤和二齿新蚤与气象因子的最优回归子集(P<0.0007、P<0.01), 月蒸发量是影响秃病蚤的最重要因子。⑦ 春季与冬季、夏季与冬季巢蚤指数差异显著(P<0.05); 春季与冬季、夏季与冬季体蚤指数差异显著(P<0.05); 春季与冬季、夏季与秋季、夏季与冬季洞干蚤指数差异显著(P<0.05)。     

二齿新蚤和方形黄鼠蚤松江亚种吸血习性的实验室观察

1983—1989年对二齿新蚤和方形黄鼠蚤松江亚种几种吸血习性进行了实验观察。1.新羽化蚤吸血蚤百分率与羽化后时间呈直线正相关。二齿新蚤至30小时左右,方形黄鼠蚤松江亚种至40小时左右,吸血蚤百分率约达90%,相当于繁殖蚤。2.蚤同宿主接触5分钟内即有部份吸血。接触半小时吸血蚤数最多,半小时至1小时吸血蚤数减少,也有少部份蚤至1小时尚未吸血。3.吸血蚤与未吸血蚤均可留于宿主体上,亦均能随时离开宿主体。     

黄鼠体蚤和宿主密度的年间动态关系

根据内蒙古自治区正镶白旗乌宁巴图苏木1981-1993年达乌尔黄鼠Citellus dauricus密度和体蚤指数监测资料进行分析,得到如下结果。共检体蚤10种,其中方形黄鼠蚤蒙古亚种Citelloilus tesquorum mongoJicus(72.38%)和光亮额蚤Fronto Psylla luculenta(18.03%)分别为优势和次优势蚤种,阿巴盖新蚤Neopsylla abagaitui、二齿新蚤Neopsylla bidentatifor-mis为常见种,余为少见种。宿主密度与蚤指数均呈指数增长,鼠密度与蚤指数的关系是极为显著的(P<0.0001),关系为鼠密度＝exp(-0.6206十0.1989t),蚤指数＝1.6109+0.8997(鼠密度)。方形黄鼠蚤蒙古亚种比例的高低显著地影响体蚤的多样性和均匀性.宿主 密度与染蚤率呈正相关关系(P相似文献   

Electrostatic state of the cytoplasmic domain influences inactivation at the selectivity filter of the KcsA potassium channel

KcsA is a proton-activated K⁺ channel that is regulated at two gates: an activation gate located in the inner entrance of the pore and an inactivation gate at the selectivity filter. Previously, we revealed that the cytoplasmic domain (CPD) of KcsA senses proton and that electrostatic changes of the CPD influences the opening and closing of the activation gate. However, our previous studies did not reveal the effect of CPD on the inactivation gate because we used a non-inactivating mutant (E71A). In the present study, we used mutants that did not harbor the E71A mutation, and showed that the electrostatic state of the CPD influences the inactivation gate. Three novel CPD mutants were generated in which some negatively charged amino acids were replaced with neutral amino acids. These CPD mutants conducted K⁺, but showed various inactivation properties. Mutants carrying the D149N mutation showed high open probability and slow inactivation, whereas those without the D149N mutation showed low open probability and fast inactivation, similar to wild-type KcsA. In addition, mutants with D149N showed poor K⁺ selectivity, and permitted Na⁺ to flow. These results indicated that electrostatic changes in the CPD by D149N mutation triggered the loss of fast inactivation and changes in the conformation of selectivity filter. Additionally, the loss of fast inactivation induced by D149N was reversed by R153A mutation, suggesting that not only the electrostatic state of D149, but also that of R153 affects inactivation.     

Deleterious mutation in related species of the plant genus Amsinckia with contrasting mating systems

Theory for the evolution of modifiers of the rate of mutation suggests that a lower rate of mutation may evolve after the breakdown of mechanisms that enforce outcrossing. Mutation accumulation (MA) experiments were conducted to compare deleterious mutation parameters in two closely related species of the plant genus Amsinckia, a group that exhibits wide variation in the mating system. One of the two species studied (A. douglasiana) is predominantly outcrossed in natural populations, where as the other species (A. gloriosa) is predominantly self-pollinated. Progeny assays of flower number per plant from generation 1 lines (control) and generation 11 lines (MA treatment) were conducted in both species. Dry weight measurements of progeny from the control and MA treatment in A. douglasiana also were made. Estimation of mutation parameters was conducted using maximum likelihood under the assumption of a gamma distribution of mutational effects. The two species exhibited similar rates and effects of deleterious mutation affecting flower number. Estimates of mutation rate for dry weight in A. douglasiana are close to those for flower number. Overall, the estimates of mutation parameters observed in these species are intermediate within the range reported for fitness components in other eukaryotes. The results are discussed within the context of evolutionary change in deleterious mutation accompanying mating system evolution and with respect to previous estimates of mutation parameters based on assays of inbreeding depression and the assumption of mutation-selection equilibrium.     

The effect of mutations in alpha-tropomyosin (E40K and E54K) that cause familial dilated cardiomyopathy on the regulatory mechanism of cardiac muscle thin filaments

E40K and E54K mutations in alpha-tropomyosin cause inherited dilated cardiomyopathy. Previously we showed, using Ala-Ser alpha-tropomyosin (AS-alpha-Tm) expressed in Escherichia coli, that both mutations decrease Ca(2+) sensitivity. E40K also reduces V(max) of actin-Tm-activated S-1 ATPase by 18%. We investigated cooperative allosteric regulation by native Tm, AS-alpha-Tm, and the two dilated cardiomyopathy-causing mutants. AS-alpha-Tm has a lower cooperative unit size (6.5) than native alpha-tropomyosin (10.0). The E40K mutation reduced the size of the cooperative unit to 3.7, whereas E54K increased it to 8.0. For the equilibrium between On and Off states, the K(T) value was the same for all actin-Tm species; however, the K(T) value of actin-Tm-troponin at pCa 5 was 50% less for AS-alpha-Tm E40K than for AS-alpha-Tm and AS-alpha-Tm E54K. K(b), the "closed" to "blocked" equilibrium constant, was the same for all tropomyosin species. The E40K mutation reduced the affinity of tropomyosin for actin by 1.74-fold, but only when in the On state (in the presence of S-1). In contrast the E54K mutation reduced affinity by 3.5-fold only in the Off state. Differential scanning calorimetry measurements of AS-alpha-Tm showed that domain 3, assigned to the N terminus of tropomyosin, was strongly destabilized by both mutations. Additionally with AS-alpha-Tm E54K, we observed a unique new domain at 55 degrees C accounting for 25% of enthalpy indicating stabilization of part of the tropomyosin. The disease-causing mechanism of the E40K mutation may be accounted for by destabilization of the On state of the thin filaments; however, the E54K mutation has a more complex effect on tropomyosin structure and function.     

Molecular basis of an isogeneic anti-idiotypic response.

The nucleotide sequences of the variable region genes expressed in the heavy and light chains of six isogeneic anti-idiotope antibodies recognizing idiotopes on two closely related antibodies with specificity for the hapten (4-hydroxy-3-nitrophenyl)acetyl (NP) were determined. In two independently derived anti-idiotope cell lines the same or strongly homologous V kappa, VH and D region genes had originally been rearranged. The two lines express long and partly homologous N sequences (presumed to be not of germ line origin) at the border of D, resulting in CDR3s of unusual length. An unusually long CDR3, partly encoded by N sequences, is also present in the heavy chain of a third anti-idiotope antibody. The VH regions of the three remaining anti-idiotope antibodies originate from a single VH gene which belongs to the same VH group as the VH genes expressed in the other anti-idiotopes. Two of these antibodies, expressing similar V, D and J elements, had been isolated from the same mouse and appear to have diverged from the same B cell precursor by at least two rounds of somatic mutation. Somatic point mutations have occurred in most, if not all anti-idiotope V region sequences. In two instances somatic mutations in J increase the structural homology between anti-idiotopes. The anti-idiotypic response in this system is thus genetically restricted and may depend upon the selection of non-germ line sequences, suggesting an explanation for the low frequency at which anti-idiotope antibodies are expressed in this system.     

群居性啮齿动物集群重组率的估算

提出了一种定量估算群居性啮齿动物的集群重组率的方法。此法以特定时期集群中动物个体之间的异源概率（即来源于不同家族的概率）作为衡量群居性啮齿动物的“混合”程度（即重组率）的定量指标,并与平均重组率（即重组期望）进行比较,进而判断动物在集群过程中的选择倾向。按照这种方法估算了内蒙古典型草原区布氏田鼠越冬集群的重组率。结果表明,该鼠的越冬集群重组率很低,仅在0.1左右,集群个体多数来源于相同的家族。此外,该鼠的集群重组率远低于其重组期望值,表明该鼠在秋季集群中,有强烈的选择同源个体的倾向。