中国轮藻植物分布研究

轮藻植物是低等的藻类植物,但其个体较大、高度分化,生殖器官构造复杂,可与高等植物的性器官比较,因此将它们列为独立一门即轮藻门(Charophyta),轮藻门只有一个轮藻科(Characeae)。轮藻植物分布于除南极洲以外的所有大陆,多生于淡水,少数生长在微盐性的水体中,轮藻植物分布与环     

中国西北轮藻属新分类群

本文报道了采自甘肃、新疆及宁夏的轮藻植物,计有：2个新种(兰州轮藻Chara lanzhouensis sp. nov., 拟球状轮藻 Chara pseudoglobularis sp. nov．),1个新记录(弯枝轮藻Chara arcuatifolia Vilhelm．)。     

内蒙古中南部轮藻植物区系及分布特点

内蒙古中南部轮藻植物以温带成分占绝对优势,有较多的中国特有植物;种类以轮藻属为主,其中丛刺轮藻、灰色轮藻为本地的广布和优势种;分布以上河套平原的种类、数量最多;另外,轮藻植物的形态结构、种类组成及分布均与其生长的环境紧密相关。     

中国晚古生代轮藻化石组合

本文综述了数十年来中国晚古生代轮藻化石研究成果。与全球其它地区相比较,中国古生代轮藻化石较为丰富,可归纳为九个轮藻化石组合及三个轮藻化石层位。依据轮藻植物组成特点、演化特征以及伴生其它门类化石,论证各组合的地质时代,其中两个组合地质时代相同,属于不同的生物地理区系。     

山西轮藻属新植物

本文报道采自山西省的轮藻属植物2个新种,运城轮藻Chara yunchengensis,拟灰色轮藻C.pseudocanescens和3个中国新记录,阿尔泰轮藻C.altaica,豪威轮藻C.howeana,味美轮藻簇毛变种C.delicatula var.barbata     

尼泊尔克里雅(Churia)群之比奈科拉(Binai Khola)组下段轮藻化石的发现及其意义

该文研究的轮藻化石采自尼泊尔中西部阿龙科拉地区的比奈科拉组下段。轮藻化石有Nitellopsis (Tectochara)globula(Madler)Grambast et Soulie-Marsche,Chara molassica Straub,C.gigantofusiformis(Yang),Rantzieniella binaiensis sp.nov.,Gyrogona arungensis sp.nov.和Lychnotharnnuspseudoodea(Berger)Soulie-Marsche等,此轮藻化石植物群属新第三纪,可能为中新世晚期。克里雅群轮藻的研究将增添南亚新第三纪地质生态研究的内容。     

中国轮藻植物区系研究

中国轮藻植物有13种分布区类型,其中以中国特有分布占绝对优势,其它分布类型所占比例较低,说明中国轮藻植物与其它地区轮藻植物联系较少。丽藻属有10种分布区类型,缺少温带特性的分布区类型,如北温带分布、旧世界温带分布,其它分布区类型显示丽藻属主要分布在热带和亚热带地区,而轮藻属有13种分布区类型,温带特性的分布区类型所占比例较高,如旧世界温带分布,其它分布区类型显示轮藻属主要分布在温带地区。     

喜马拉雅前陆盆地中新世-上新世SIWALIK-CHURIA群轮藻化石及其古生物地理和古生态意义

印度、尼泊尔晚中新世-上新世SIWALIK-CHURIA群轮藻化石组合与中国塔里木盆地及哈萨克斯坦东南部伊犁盆地轮藻组合极为接近。据此讨论了它们的古生物地理和古生态学特征。中新世-上新世轮藻植物繁盛的原因与当时季风活动引起的季节性洪水泛滥,在广大河漫滩地上形成有利于轮藻植物生长发育的局部湖泊环境有关。     

青海柴达木盆地第三纪轮藻化石

一、绪言近年来轮藻化石曾发现于我国许多地区的泥盆纪、侏罗纪、第三纪和第四纪地层中,其中以青海柴达木盆地的第三纪地层发现最多。本文所描述的就是青海柴达木盆地红三旱Ⅰ号、鄂博梁Ⅰ、Ⅱ、Ⅲ号及冷湖Ⅶ号5个地区第三纪地层所产的轮藻化石,计1科、4亚科、8属、42种、6亚种和1变种,其中包括27个新种和1个新变种。柴达木盆地轮藻化石的分布以盆地中心最为丰富,如鄂博梁Ⅱ号、Ⅲ号及冷湖Ⅶ     

轮藻—观察原生质和精子运动的好材料

在具真核的淡水藻类中,轮藻属(Chara)是一种结构复杂、进化水平较高的类群,它们在植物系统学教学和科研中是不可缺少的典型材料。笔者在教学实践中发现,轮藻也是观察植物活细胞原生质流动及游动精子的最佳材料。由于轮藻在室内栽     

Two complementary perspectives on inter-individual genetic distance

This paper examines population structure through the prism of pairwise genetic distances. Two complementary perspectives, framed as two simple questions, are explored: Q1: What is the probability that a random pair of individuals from the same local population is more genetically dissimilar than a random pair from two distinct populations? Q2: On average, how genetically different are two individuals from the same local population, in comparison with two individuals chosen from any two distinct populations? Models are developed to provide quantitative answers for the two questions, given allele frequencies across any number of markers from two diploid populations. The probability from Q1 is shown to drop to zero with increasing number of genetic markers even for very closely-related populations and rare alleles. The average genetic dissimilarity of two individuals from distinct populations diverges from the average dissimilarity of two individuals from the same population by a percentage dependent on estimates of population differentiation. This perspective also suggests a measure of population distance based on the intuitive notion of pairwise genetic distance, along with a simple method of estimation. Results from recent empirical research on inter-individual genetic distance in human populations are analyzed in the context of the theoretical framework.     

PERMANENT GENETIC RESOURCES: Development of microsatellite markers for two nonviviparous mangrove species, Acanthus ilicifolius and Lumnitzera racemosa

Eight and nine of microsatellite loci were isolated from two nonviviparous mangrove species, Acanthus ilicifolius and Lumnitzera racemosa, respectively. The number of alleles per locus ranged from two to eight in A. ilicifolius and two to nine in L. racemosa. The observed heterozygosities ranged from 0.200 to 0.875 in A. ilicifolius and from 0.025 to 0.350 in L. racemosa. These loci would be effective for analysing genetic diversity and population genetic structure of these two mangrove species.     

New polymorphic microsatellite loci for population studies in the European anchovy, Engraulis encrasicolus (L.)

Eleven microsatellite loci were developed in the European anchovy, Engraulis encrasicolus, and tested in samples from two geographically distant populations (Atlantic and Mediterranean Sea). Number of alleles ranged from eight to 28 and observed heterozygosity from 0.440 to 0.920. There was no evidence of linkage disequilibrium, although two loci are indeed linked. All loci were in Hardy-Weinberg equilibrium, except for one locus in the Atlantic and two loci in the Mediterranean sample. These three loci plus two more showed evidence for null alleles.     

台闽苣苔（苦苣苔科）花部器官的形态发生

在扫描电镜下对台闽苣苔 (T .oldhamii (Hemsl.)Solereder)进行了花部器官形态发生的观察 ,为探索该类群的个体发育、类群间的系统发育关系和进化趋势提供依据。研究发现该属植物萼片、花冠和雄蕊发生式样均为五数花类型 ,它们各自来源于花原基上分化出来的萼片原基、花冠原基和雄蕊原基 ;花冠与雄蕊的两侧对称性与花冠上唇生长稍快和退化雄蕊原基发育迟滞相关 ;萼片原基的发生和发育的顺序是不一致的 :萼片原基发生的式样为近轴中原基—远轴 2原基— 2侧原基 ,发育式样则为近轴中萼片— 2侧萼片—远轴 2萼片 ,花蕾时为镊合状排列。花冠裂片原基的发生和发育式样是一致的 ,即远轴中裂原基 (下唇中裂片 )—远轴 2侧裂原基 (下唇 2侧裂片 )—近轴 2裂原基 (上唇 2裂片 )。花蕾期卷迭式为覆瓦状排列 ,从外向内 :下唇中裂片—下唇 2侧裂片—上唇 2裂片或下唇 2侧裂片—上唇 2裂片—下唇中裂片。雄蕊原基与花冠裂片原基互生 ,前方雄蕊原基在发生上稍迟于后方雄蕊原基 ,后者与退化雄蕊原基几乎同时发生 ,但较小 ,并与近轴心皮 (或柱头上唇 )对生。将该属与玄参科 (Scrophulari aceae)的地黄属 (Rehmannia)、苦苣苔科 (Gesneriaceae)的异叶苣苔属 (Whytockia)和尖舌苣苔属 (Rhynchoglossum)的花部器官比较发现     

Pairwise differences under a general model of population subdivision

A number of different migration and isolation models of population subdivision have been studied. In this paper I analyse a general model of two populations derived from a common ancestral population at some time in the past. The two populations may exchange migrants, but they may also be completely isolated from each other. I derive the expectation and variance of the number of differences between two sequences sampled from the two populations. These are then compared to the corresponding results from two other much-used models: equilibrium migration and complete isolation.     

Genetic diversity of Gambierdiscus spp. (Gonyaulacales, Dinophyceae) in Japanese coastal areas

The genetic diversity of the ciguatera fish poisoning-related dinoflagellate distributed in Japanese coastal areas was investigated. The entire sequence of the 5.8S rRNA gene and two internal transcribed (ITS) regions were determined, which included putative pseudogenes, from 19 strains of dinoflagellates assigned to the genus Gambierdiscus Adachi et Fukuyo collected from Japanese subtropical and temperate coastal areas. The sequences obtained from the 19 strains were divided into two types based on sequence similarity. Here we designate the two types as type 1 and type 2. For the relationship between the genotypes and origins of the strains used, the strains collected from subtropical areas possessed the type 1 sequence; whereas those from temperate areas possessed the type 2. This observation led us to question former reputations that Gambierdiscus cells observed in Japanese temperate areas are immigrants from Japanese subtropical areas. Subsequently, we sequenced a part of the 18S rRNA gene from two strains from subtropical areas and two from temperate areas. Unfortunately, phylogenetic analysis including the sequences obtained from various gonyaulacales dinoflagellates failed to determine the species phylogenetically closely related to and possible origin(s) of the Gambierdiscus sp. from the Japanese coastal areas.     

Comparison of Established Cell Lines at Different Passages by Karyotype and Comparative Genomic Hybridization

Two established cancer cell lines, MCF-7 and Ishikawa, were both obtained directly from a cell repository and through another laboratory. The karyotypes from the two MCF-7 cell lines had up to 83 chromosomes and similarities for chromosomal gain and structural abnormalities. The two Ishikawa cell lines had up to 60 chromosomes with only a missing X as the common chromosome abnormality. CGH studies were performed by co-hybridizing the two Ishikawa or MCF-7 cell lines to normal metaphases. The differences seen between the two MCF-7 cell cultures reflect changes due to passage number and culture conditions. For Ishikawa, DNA polymorphic data and mutation studies suggest that the two cell lines are not derived from the same established tumor cell line. Our study shows the utilization of CGH in comparing cell lines originating from the same specimen. Our study also demonstrates the necessity for periodically evaluating cell lines to confirm their origin.     

The genus Unixenus Jones, 1944 (Diplopoda, Penicillata, Polyxenida) in Australia

The penicillate genus Unixenus Jones, 1944 is widespread, with species found in Africa, Madagascar, India and Australia. Each of the two Australian species was originally described from single samples from Western Australia. In this study, collections of Penicillata from museums in all states of Australia were examined to provide further details of the two described species, to revise the diagnoses for both the genus and the species, and to better understand the distribution of the two species in Australia. In addition, two new species Unixenus karajinensissp. n. and Unixenus corticolussp. n. are described.     

Isolation and characterization of microsatellite loci in the plant-ant Pseudomyrmex ferrugineus (Formicidae: Pseudomyrmecinae) and cross-testing for two congeneric species

To investigate the population structure of the obligate plant-ant Pseudomyrmex ferrugineus, we developed primers for 12 microsatellite loci. We tested the variability of the markers on 11 individuals from each of two populations (totalling 22 individuals) and found two to 12 alleles per locus and population. No deviations from Hardy-Weinberg equilibrium were detected. Observed and expected heterozygosities at each locus ranged from 0.00 to 0.50 and from 0.08 to 0.46, respectively. We also investigated suitability of these primers in two congeneric species.     

Microdissection and PCR Amplification of Single Soybean Chromosome

Glass needles were successfully used to dissect the soybean (Glycine max L. ) single chromosome under the micromanipulator in this research. Two dissected soybean chromosomes were digested by Sau3A in two 0.5 mL Eppendorf tubes respectively. The two ends of chromosomal fragments were ligated with Sau3A linker adoptor. After two rounds of PCR amplification, smear DNA fragments ranged from 0.3 to 3 kb were acquired. Southern hybridization result showed the PCR products from the two single soybean chromosomes were homogeneous with the soybean genomic DNA, indicating that DNAs from the two single chromosomes have been successfully amplified. At the same time, the amplified products from the two of the distinguished single chromosome appeared somewhat different. The authors dissected the small chromosomes only by a traditional inverted microscope. Therefore, this research provides a plausible chance for amplification and microcloning of single small chromosomes.