广西窄腹茧蜂属一新种：膜翅目：茧蜂科：茧蜂亚科

茧蜂亚科已知有123个属(Quicke,1987),其中窄腹茧蜂属Angustibracon Quicke是Quicke(1987)根据分布在印度的1个种Bracon leptogaster Cameron重新组合为1个新属而建立,迄今已定名种仅此1种。我们整理广西茧蜂标本时,鉴定出该属1新种。这是本属种类在我国分布的首次报道,现将该属属征和新种形态记述如下。新种模式标本存湖南农学院昆虫标本室。     

寄生云杉树蜂的枝跗瘿蜂一新种(膜翅目:瘿蜂总科:枝跗瘿蜂科)

枝跗瘿蜂科(Ibahidae)是个小科,所有种类均寄生蛀干害虫树蜂科(Siricidae)的幼虫。我国大陆的本科种类由杨忠岐1991年首次作了报道。现记述采自祁连山林区的另1新种。该种寄生于为害青海云杉(Picea crassifolia Kom.)的黄肩长尾树蜂(Xeris spec-trum spectrum)等树蜂的幼虫。新种的模式标本保存于西北林学院天敌昆虫研究室。至此,我国大陆共有本科种类3种,加上台湾的1个种,我国共有4种:     

吉林省跃度蝗属一新种：直翅目：网翅蝗科

本文报道跃度蝗属1新种。模式标本保存于东北师范大学生物系动物标本室。1.土们岭跃度蝗Podismopsis tumenlingensis,新种 雄性:体小型。头顶三角形,具中隆线,眼间距宽为触角间颜面隆起宽的2.00-2.26倍。缺头侧窝。颜面倾斜,颜面隆起侧缘近平行,中央具纵沟。触角丝状,     

云南所麻蝇属一新种记述：双翅目：麻蝇科

作者在整理1985年采集的麻蝇科标本中,发现所麻蝇属(SarcosolomoniaBaranov)1新种。模式标本分别保存于云南省卫生防疫站和军事医学科学院微生物流行病研究所。     

绿褶托菇在我国首次发现

本文报道我国蘑菇科Agaricaceae的一个新记录种——绿褶托菇Clarkeinda trachodes (Berk.)Singer,该种所隶属的绿褶托菇属Clarkeinda O. Kuntze现知是个分布于热带亚洲的单型属。     

中国紫堇属大叶紫堇组的分类与分布

本文叙述大叶紫堇组在紫堇属(Corydalis)中的系统位置以及其分布区的原始性,同时记载了隶属于5个系的23种9变种和1变型,其中有4个新系,7个新种和7个新变种。     

The biogeography of three Boeckella species (Copepoda: Calanoida) in New Zealand

The New Zealand distributions of three species of Boeckella (Copepoda, Calanoida), B. triarticulata, B. dilatata and B. hamata are mapped. B. triarticulata is primarily a pond dweller but is also found in reservoirs and shallow lakes. B. dilatata is mainly found in the deeper glacial lakes and ponds in the central region of the South Island and B. hamata has a more widespread distribution in lakes and ponds in the South Island and lower half of the North Island. Differences in temperature optima, food requirements and dispersal ability among the three Boeckella species are related to vicariant events to explain their distribution in New Zealand.     

Inhibition of cell proliferation with antibody-targeted liposomes containing methotrexate-γ-dimyristoylphosphatidylethanolamine

We have prepared liposomes containing methotrexate-γ-dimyristoylphosphatidylethanolamine (MTX-DMPE liposomes), to which protein A was covalently coupled, permitting specific association of these liposomes in vitro with murine cells preincubated with relevant protein A-binding monoclonal antibodies. In the absence of antibody the presence of externally-oriented methotrexate (MTX) in MTX-DMPE liposomes did not result in greater binding to cells than liposomes made without MTX-γ-DMPE. Derivation of methotrexate with phospholipid permits enhanced drug-liposome association. These liposomes are more resistant than conventional liposomes to repeated cycles of freezing and thawing. MTX-DMPE liposomes are comparable to antibody-targeted liposomes made with encapsulated water-soluble methotrexate both with respect to specific binding to target cells and drug effect. The inhibitory effects off MTX-liposomes, as well as free MTX, were reversible by either thiamin pyrophosphate (Tpp) or N⁵-formyltetrahydrofolate (F-THF), while the effects of MTX-DMPE liposomes were reversed only by N⁵-formyltetrahydrofolate. This suggests that the toxicity of non-targeted MTX-liposomes may be due to leakage of the encapsulated MTX. The absence of an effect of thiamin pyrophosphate on non-targeted MTX-DMPE liposomes indicates that they do not enter into the cell via the normal folate transport system.     

Convergence of genetic distances in a migration matrix model

A recurring problem with the use of migration matrix models of genetic differentiation has to do with their convergence properties. In practice, predictions can be drawn from these models only at equilibrium; but in the case of the standard predictors (most of which are modifications of Wright's FST), it can take an unrealistically large number of generations to approach equilibrium. An alternative set of predictors, the set of all pairwise genetic distances among the populations that define the rows and columns of the migration matrix, is investigated here. These distances are shown analytically to converge much more rapidly than the more commonly used predictors. In an application of the model to migration data on a human population from Papua New Guinea, it takes only about three to four generations for the pairwise distances to converge, in contrast to more than 100 generations for one of the standard predictors. In this case, moreover, the distances predicted by the model at equilibrium are similar to those calculated from the available genetic data.     

The isolation and characterization of ngm2, a mutation that affects nitrosoguanidine mutagenesis in yeast

Summary We have isolated and characterized a new mutant of Saccharomyces cerevisiae, carrying a single mutant allele that we designate ngm2-1, which is defective with respect to induced mutagenesis. This mutant was isolated by screening mutagenized clones for reduced frequencies of reversion of the his1-7 allele, induced by N-methyl-N-nitro-N-nitrosoguanidine. As judged by the reversion of his1-7 and ilv1-92, ngm2-1 mutant strains are also deficient with respect to mutability induced by methyl methane sulfonate, ethyl methane sulfonate and, at least partially, by UV. UV-induced reversion of the ochre mutation arg4-17 and the frameshift mutation his4-38 was not much affected by ngm2-1, however. Like rev3 and rev7 mutations, ngm2-1 also has little influence on the reversion of the proline missense allele, cyc1-115. Ngm2-1 mutants are only at best very slightly more sensitive to the toxicity of the four mutagens used, and homozygous diploids sporulate normally.