内蒙古呼伦贝尔草原多房棘球蚴病病原的调查

本文报道在内蒙古呼伦贝尔草原主体部分四个牧业旗的草场进行多房棘球蚴病病原调查的结果。发现布氏田鼠(Microtus brandti)及长爪沙鼠(Meriones unguicutatus)是本绦虫的中间宿主、沙狐(Vulpes corsac)是其终末宿主。布氏田鼠是本绦虫中间宿主新记录,长爪沙鼠和沙狐分别是国内本绦虫中间宿主和终宿主新记录。布氏田鼠是呼伦贝尔草原的优势啮齿类,其平均感染率为2.43％(64/2635),越冬成鼠感染率高达5.23％—14.29％(平均6.66％)。长爪沙鼠感染率虽达16.67％(1/6),但鼠数不多。沙狐是本草原常见的食肉兽,检查6只沙狐,其中2只(33.3％)肠内含多房棘球绦虫成虫无数。用其孕节饲喂实验室小白鼠6只,6个月后检查各实验鼠,肝脏均布满泡状多房棘球蚴。呼伦贝尔草原本绦虫成虫及原头节形态特征均与我国西北本虫种差异显著,而与苏联及美国阿拉斯加的多房棘球绦虫西伯利亚亚种比较相似。     

内蒙古草原五种啮齿动物肾脏形态学特征比较

啮齿动物的水平衡能力对其适应干旱环境至关重要。为理解啮齿动物对水环境的适应性,本研究以分布于内蒙古草原的长爪沙鼠 (Meriones unguiculatus)、布氏田鼠 (Lasiopodomys brandtii)、小毛足鼠 (Phodopus roborovskii)、坎氏毛足鼠 (Phodopus campbelli) 和黑线仓鼠 (Cricetulus barabensis) 为研究对象,测定了肾脏形态学指标、肾单位密度指标和尿液渗透压等,比较分析了肾脏形态结构与栖息地环境之间的关系。结果发现：5种啮齿动物肾脏髓质厚度随动物分布区域的变化,呈现从典型草原地区、半荒漠地区至荒漠和沙漠地区逐渐增加的趋势,干旱地区动物的尿液渗透压较高。5种动物的皮质肾单位密度无显著差异。近髓肾单位密度统计显示,黑线仓鼠大于小毛足鼠与坎氏毛足鼠,布氏田鼠与长爪沙鼠居中。这些结果表明,啮齿动物的肾脏形态指数和组织学指数可以在一定程度上反映哺乳动物肾脏浓缩尿液的能力,肾脏的结构具有可塑性以应对环境的变化。     

年龄对布氏田鼠和长爪沙鼠能量代谢的影响

能量代谢对动物的存活和繁殖等生活史特征具有重要的调控作用.布氏田鼠(Lasiopodomys brandtii)和长爪沙鼠(Meriones unguiculatus)是内蒙古草原同域分布的两种啮齿动物,前者的体重和野外寿命要明显小于后者,这符合寿命随体型增大而增加的一般规律.本研究进一步探讨了随年龄增加,两种动物的能量代谢特征的改变.发现布氏田鼠的非颤抖性产热能力随年龄增加而降低,而长爪沙鼠的非颤抖性产热能力随年龄增加而保持稳定.布氏田鼠的摄食能力和身体脂肪储备随年龄增加而降低;而长爪沙鼠摄食能力不随年龄改变,脂肪储备则随年龄增加而增加.长爪沙鼠的基础代谢水平低于布氏田鼠,其繁殖成熟时间更长.本研究推测,这些随年龄而变的生理特征反映了两种动物不同的生活史对策:布氏田鼠更倾向于尽快繁殖,其他与生存相关的生理指标随年龄增加而迅速降低,而长爪沙鼠更倾向于将能量投资到较晚期的存活和繁殖.     

内蒙古草原布氏田鼠和长爪沙鼠体重及身体成分的季节变化

研究了内蒙古草原布氏田鼠(Lasiopodomys brandtii)和长爪沙鼠(Meriones unguiculatus)的体重、身体脂肪、水分含量及身体热值等指标的季节变化.2种动物的体重都是在春季最高,布氏田鼠的体重具显著的季节变化,长爪沙鼠的鲜重具季节变化,但干重则基本维持恒定.2种动物的脂肪含量和身体热值都...     

光周期对布氏田鼠和长爪沙鼠体重和能量代谢的影响

本文测定了光周期对雄性布氏田鼠和长爪沙鼠的体重、基础代谢率和能量代谢的影响。动物从长光照(16L∶8D , LD) 转入短光照(8L∶16D , SD) 条件下驯化6 周(田鼠) 和7 周(沙鼠) 。结果显示: (1) 无论在LD还是SD 条件下, 两种动物的体重都趋于增加, 但反应程度不同也具有种间差异性。两种动物的体重对光周期的反应有时段性, 约14 d 前两种动物的体重增加迅速, 而后增加缓慢, 3 周左右趋于稳定。短光照条件下布氏田鼠和长爪沙鼠的体重分别增长了37 %和11 % , 均低于长光照组(分别为47 %和25 %) , 说明短光照条件下布氏田鼠和长爪沙鼠的体重增长较长光照缓慢; (2) 光照对两种动物的摄入能、消化能和可代谢能均没有显著影响,摄入能与体重的增长无关; (3) 光照对两种动物的基础代谢率无显著影响。这些结果表明: 布氏田鼠和长爪沙鼠在自然环境中, 可能以光周期作为一种信号, 当环境温度降低、食物质量变劣时, 采取降低体重以减少绝对能量需求的策略而适应环境。     

长爪沙鼠对植物血凝素的反应及能量学代价的性别和季节差异

以野生长爪沙鼠为对象,通过外源注射植物血凝素(Phytohemagglutinin,PHA)和磷酸盐缓冲液,分别测定了夏季和冬季沙鼠注射前、注射24 h 和48 h 后体重和静止代谢率(Resting metabolic rate,RMR)的变化,以及48 h 后沙鼠足增重量和白细胞总数(White blood cell counts,WBCs)的变化,以检测沙鼠的免疫功能和能量代价的性别和季节差异。结果显示:1)注射PHA 能显著增加沙鼠足重和白细胞的总数,夏季白细胞的总数高
于冬季;2)冬季沙鼠体重高于夏季,雄鼠大于雌鼠,但PHA 处理对注射前后沙鼠的体重无影响;3)冬季RMR高于夏季,雄鼠大于雌鼠,但PHA 处理对沙鼠的RMR 无影响,PHA 处理对注射前后沙鼠的RMR 也无影响。这些结果表明,长爪沙鼠对PHA 的反应具有季节差异,但无性别差异,也没有发现明显的能量学代价,这可能与野外环境条件的大幅度波动(如环境温度和食物条件等)和沙鼠的繁殖状态有关。     

长爪沙鼠的一些生态学资料

长爪沙鼠(Meriones unguiculatus)是荒漠草原分布较广的害鼠。夏武平(1982)、赵肯堂(1960)等对长爪沙鼠的某些生态方面进行了研究。作者从1979年5月至1980年6月在宁夏陶乐县对长爪沙鼠的数量季节变动、迁徒、繁殖、年龄组成、食性等方面进行了调查研究,现报告于后。     

炔雌醚对内蒙古农牧交错带长爪沙鼠(Meriones unguiculatus)家群大小和巢域行为的影响

为检验施用炔雌醚对农牧交错带长爪沙鼠家群大小与巢域行为的影响,于2006年5月至9月对内蒙古锡林郭勒盟锡林浩特市农牧交错区域分布的长爪沙鼠家群使用炔雌醚进行种群不育控制实验。分设投药区和对照区两个组别,分别于5月、7月与9月份采用1/4样圆面积有效洞口计数法,随机选取24个长爪沙鼠家群,调查对照区域和投药区内沙鼠的家群洞口数量以及家群大小。另在对照区和投药区,随机测定了30个沙鼠的家群活动范围,对比使用炔雌醚前后长爪沙鼠巢域平均半径和活动面积的影响。结果为:对照区家群平均洞口数58个,投药区仅23个,在炔雌醚投药区长爪沙鼠家群受炔雌醚影响,洞口数仅为23个,表明其对长爪沙鼠家群大小控制效果显著。投药区内长爪沙鼠家群密度在投药后连续下降,最大下降幅度较对照区家群密度低70%,表明炔雌醚对长爪沙鼠的家群密度影响较大,可显著降低长爪沙鼠家群密度(P<0.05)。炔雌醚对长爪沙鼠家群平均半径和活动面积的研究结果显示,施用炔雌醚后家群巢域半径与活动面积均显著缩小(P<0.05),与对照区巢域平均面积相比缩小15%、平均活动半径缩小30%。通过以上结果可得出:单独施用炔雌醚对控制野外长爪沙鼠家群以及降低长爪沙鼠巢域、活动面积效果显著。炔雌醚可有效降低农牧交错带长爪沙鼠种群数量和有效活动范围,这对于农牧交错带的鼠害防控,同时降低鼠源性疾病,包括鼠疫的传播都有一定的意义。     

内蒙古察哈尔丘陵啮齿动物种群数量的波动和演替

根据内蒙古自治区正镶白旗乌宁巴图苏木９７４－１９９３年随啮齿动物密度监测资料进行分析,得到如下结果。共捕啮齿动物１３种,其中达乌尔黄鼠为优势种（６７．８５％）、一趾鼠为次优势种（１０．１６％）,长爪沙鼠、布氏田鼠、达乌尔鼠兔为常见种,余为少见种。黄鼠密度与个体数呈正相关（Ｐ〈０．０００１）、五趾跳鼠与个体数、黄鼠密度呈负相关（Ｐ〈０．００１）。个体数与黄鼠、五趾跳鼠密度的回归模型为：（个体数）＝１     

草颗粒灭鼠诱饵的性能

草颗粒原是把牧草加工成颗粒饲料饲喂牲畜的,我们于1975—1978年先后在内蒙、甘肃等地用它作诱饵对布氏田鼠(Microtus brandti)、达乌尔黄鼠(Citellus dauricus)、高原鼠兔(Ochotona curzoniae)和长爪沙鼠(Meriones unguiculatus)作了灭鼠试验。试验表明,在我国北方草原上可以用草颗粒代粮灭一些草食性鼠类。实践中遇到一些问题,有必要了解草颗粒的性能,几年来就影响草颗粒灭鼠效果的有关因素作了试验,现整理如下。     

Copper (II) and cobalt (II) complexes of chiral tetrathiafulvalene-oxazoline (TTF-OX) and tetrathiafulvalene-thiomethyl-oxazoline (TTF-SMe-OX) derivatives

Synthesis and single crystal X-ray structures of the first paramagnetic transition metal complexes containing chiral ethylenedithio-tetrathiafulvalene-oxazoline (EDT-TTF-OX) 1a-c and ethylenedithio-tetrathiafulvalene-thiomethyloxazoline 2 (EDT-TTF-(SMe)OX) ligands based on copper (II) and cobalt (II) are described. The racemic [EDT-TTF-OX][Cu(hfac)₂] complex 3a crystallizes in the triclinic centrosymmetric space group , whereas the enantiopure counterparts 3b-c crystallize in the triclinic non-centrosymmetric space group P1. Cu(II) adopts a distorted square pyramidal coordination geometry, a much weaker Cu?S_TTF interaction also being identified. The same coordination pattern around Cu(II) is observed in the complex [(rac)-EDT-TTF-(SMe)OX][Cu(hfac)₂] (4) in spite of the bidentate nature of the redox active ligand. DFT theoretical calculations afforded two equilibrium configurations for a corresponding model complex, in which the metal centre establishes secondary coordination either with one S_TTF or with the SMe group. The same ligand coordinates the cobalt (II) to afford the octahedral complex [(rac)-EDT-TTF-(SMe)OX][Co(hfac)₂] (5). In all these novel complexes, the paramagnetic centres are structurally and magnetically isolated. Cyclic voltammetry measurements show the stability of the radical cation species.     

Binding of tetrakis(pyrazoliumyl)porphyrin and its copper(II) and zinc(II) complexes to poly(dG-dC)2 and poly(dA-dT)2

Interactions of cationic porphyrins bearing five-membered rings at the meso position, meso-tetrakis(1,2-dimethylpyrazolium-4-yl)porphyrin (MPzP; M is H₂, Cu^II or Zn^II), with synthetic polynucleotides poly(dG-dC)₂ and poly(dA-dT)₂ have been characterized by viscometric, visible absorption, circular dichroisim and magnetic circular dichroism spectroscopic and melting temperature measurements. Both H₂PzP and CuPzP are intercalated into poly(dG-dC)₂ and are outside-bound to the major groove of poly(dA-dT)₂, while ZnPzP is outside-bound to the minor groove of poly(dA-dT)₂ and surprisingly is intercalated into poly(dG-dC)₂. The binding constants of the porphyrin and poly(dG-dC)₂ and poly(dA-dT)₂ are on the order of 10⁶ M⁻¹ and are comparable to those of other cationic porphyrins so far reported. The process of the binding of the porphyrin to poly(dG-dC)₂ and poly(dA-dT)₂ is exothermic and enthalpically driven for H₂PzP, whereas it is endothermic and entropically driven for CuPzP and ZnPzP. These results have revealed that the kind of the central metal ion of metalloporphyrins influences the characteristics of the binding of the porphyrins to DNA.Electronic Supplementary Material Supplementary material is available for this article at and is accessible for authorized users.     

Synthesis and properties of trinuclear polypyridyl complexes Ru(II)-Co(II)-Ru(II) and Ru(II)-Co(III)-Ru(II): Their photoinduced interconversion

The trinuclear [{Ru^II(bpy)₂(bpy-terpy)}₂Co^II]⁶⁺ complex (1⁶⁺) in which a Co(II)-bis-terpyridine-like centre is covalently linked to two Ru(II)-tris-bipyridine-like moieties by a bridging bipyridine-terpyridine ligand has been synthesised and characterised. Its electrochemical, photophysical and photochemical properties have been investigated in CH₃CN. The cyclic voltammetry exhibits two successive reversible oxidation processes, corresponding to the Co^III/Co^II and Ru^III/Ru^II redox couples at E_1/2 = −0.06 and 0.91 V vs Ag/Ag⁺ 10 mM, respectively. The one-electron oxidized form of the complex, [{Ru^II(bpy)₂(bpy-terpy)}₂Co^III]⁷⁺ (1⁷⁺) obtained after exhaustive electrolysis carried out at 0.2 V is fully stable. 1⁶⁺ and 1⁷⁺ are only poorly luminescent, indicating that the covalent linkage of the Ru(II)-tris-bipyridine centre to the cobalt subunit leads to a strong quenching of the Ru^II excited state by an intramolecular process. Luminescence lifetime experiments carried out at different temperatures indicate that the transfer is more efficient for 1⁷⁺ compare to 1⁶⁺ due to lower activation energy. Continuous irradiation of 1⁷⁺ performed at 405 nm in the presence of P(Ph)₃ acting as sacrificial electron donor leads to its quantitative reduction into 1⁶⁺, whereas similar experiment starting from 1⁶⁺ with a sulfonium salt as sacrificial electron acceptor converts 1⁶⁺ into 1⁷⁺ with a slower rate and a maximum yield of 80%. These photoinduced electron transfers were followed by UV-Visible spectroscopy and compared with those obtained with a simple mixture of both mononuclear parent complexes i.e. [Ru^II(bpy)₃]²⁺ and [Co^II(tolyl-terpy)₂]²⁺ or [Co^III(tolyl-terpy)₂]³⁺ (tolyl-terpy = 4′-(4-methylphenyl)-2,2′:6′,2′′-terpyridine).     

Sericolophus (Pheronematidae) and Hernandeziana (Corythophoridae) are synonyms (Hexactinellida: Porifera)

Eight specimens of Sericolophus reflexus (Ijima) were compared with the holotype of Hernandeziana ijimae (Hernandez) to assess suspected synonymy of these taxa. An extensive morphometric analysis of the spicules available in these specimens of variable condition show that the H. ijimae holotype exhibits characters near the centre of the range of S. reflexus. It is concluded that H. ijimae is a junior synonym of S. reflexus , and that the family Corythophoridae de Laubenfels is invalid by preoccupation of its base generic name.     

The helix-coil transitions of poly (dA)-poly (dT) and poly (dA-dT)-poly (dA-dT)

Helix–coil transition curves are calculated for poly (dA) poly(dT) and poly (dA-dT) poly (dA-dT) using the integral equation approach of Goel and Montroll.⁵ The transitions are described by the loop entropy model with the exponent of the loop entropy factor, k, remaining an arbitrary constant. The theoretical calculations are compared with experimental transition curves of the two polymers. Results indicate that the stacking energies for these two polymers differ by about 1 kcal/mole of base pairs. Also, a fit between theory and experiment was not possible for k > 1.70.     

The larval head of Exechia (Mycetophilidae) and Bibio (Bibionidae) (Diptera)

Exechia and Bibio have retained several plesiomorphic groundplan features of Diptera and Bibionomorpha, including a fully exposed and sclerotized head capsule, the transverse undivided labrum, the absence of movable premandibles, and undivided mandibles without combs. The fusion of the hypostomal bridge with the head capsule and largely reduced antennae are derived features shared by both taxa. The absence of teeth at the anterior hypostomal margin is a potential autapomorphy of Bibionomorpha. A basal position of Anisopodidae is suggested by a number of plesiomorphies retained in this family. Apomorphies of Bibionomorpha excluding Anisopodidae are the reduction of tentorial elements, the partial fusion of the labrum and clypeus, one-segmented antennae, the absence of a separate submental sclerite, the loss of the labial palpus, and the reduction of the pharyngeal filter apparatus. Head structures of Bibio are largely unmodified. The subprognathous orientation is one of few autapomorphic features. In contrast, the mouthparts of Exechia are highly modified in correlation with the specialized food uptake. The rasping counterrotating movements of maxillae and mandibles with teeth oriented in opposite directions are carried out by strongly developed extensors and flexors of the paired mouthparts. The modified labium mechanically supports the “drill head” formed by the mandibles und maxillae. The necessary stability of the head capsule is provided by the hypostomal bridge which also compensates the far-reaching reduction of the tentorium.     

Bis(oxalato)dioxovanadate(V) and Bis(oxalato)oxoperoxo-vanadate(V) Complexes: Spectroscopic Characterization and Biological Activity

Two structurally related vanadium(V) complexes, K₃[VO₂(C₂O₄)₂]·3H₂O and K₃[VO(O₂)(C₂O₄)₂]·1/2H₂O, were thoroughly characterized by infrared, Raman, and electronic spectroscopies. The effect of both complexes on the viability of the human MG-63 osteosarcoma cells was tested using the MTT assay. The monoperoxo complex shows a very strong antiproliferative activity (at 100-μM concentration, this complex diminished the cell viability ca. 80 %), whereas the dioxo complex was inactive.     

Specific and dual antagonists of alpha(4)beta(1) and alpha(4)beta(7) integrins.

N-(3,5-Dichlorophenylsulfonyl)-(R)-thioprolyl biarylalanine 10a has been identified as a potent and specific antagonist of the alpha(4)beta(1) integrin. Altering the configuration of thioproline from R to S led to a series of dual antagonists of alpha(4)beta(1) and alpha(4)beta(7), and the N-acetyl analogue 8b was found to be the most potent dual antagonist. A binding site model for alpha(4)beta(1) and alpha(4)beta(7) is proposed to explain the structure-activity relationship.