蝽科精巢细胞减数分裂染色体行为及其反映的属种间亲缘关系

为探讨蝽科精巢细胞减数分裂各时期染色体形态和行为差异, 以及据此反映的属种间亲缘关系, 采用常规染色体制片法对蝽科6属9种精巢细胞减数分裂各期染色体形态特征、 行为及精子的形成进行了观察和比较研究。结果表明： 蝽科精巢细胞为交叉型减数分裂, “O”型交叉为其典型交叉减数分裂形式。各属种减数分裂各期染色体行为相似, 但形态不同。减数分裂各期染色体形态、 排列方式, 中期染色体相对长度、 组成与核型以及精子形态等特征具有属种间差异性。蝽科精巢细胞中期Ⅰ染色体组平均相对长度都为12.5, 在进化过程中染色体组长度信息总量不变。基于染色体相对长度的聚类分析结果显示, 菜蝽属Eurydema、 麦蝽属Aelia、 珠蝽属Rubiconia和条蝽属Graphosoma亲缘关系密切, 而二星蝽属Stollia与果蝽属Carpocoris关系较近。     

2种辉蝽的精巢和染色体研究(半翅目:蝽科)

通过探讨中国蝽科Pentatomidae辉蝽属Carbula的红角辉蝽Carbula crassiventris(Dallas,1849)和北方辉蝽C.putoni(Jakovlev,1876)的精巢形态和染色体的核型及减数分裂行为,为蝽科昆虫的细胞分类学提供新资料。采用显微形态解剖法和染色体制片法对其精巢和染色体进行观察。结果表明:2种精巢的位置、外被颜色、形状及精巢叶的数目都一致;染色体组成均为2n(♂)=14(12A+XY),具有X-Y性别决定机制。在减数分裂过程中,常染色体前减数分裂,性染色体后减数分裂且无交叉;在中期-Ⅱ,常染色体排列成环状而性染色体在环中央形成假二价体。但是,2个物种在弥散期常染色体的去固缩程度,终变期常染色体双交叉的个数及中期-Ⅰ常染色体和性染色体的排列方式都各不相同。本文证实了蝽科昆虫的减数分裂行为在不同属间、种间可不相同,而且具有一定的属、种间特异性;同时为精巢在蝽类昆虫分类中的作用提供新的资料。     

五种蝽科昆虫的细胞分类学研究（半翅目：异翅亚目）

研究了5种中国蝽科昆虫的核型和染色体的减数分裂行为,并采用核型分析软件对第一次减数分裂中期的染色体进行核型分析。结果表明：驼蝽Brachycerocoris camalus Costa、滴蝽Dybowskyia reticulata(Dallas）和红玉蝽Hoplistodera pulchra Yang3个种的染色体组成均为2n（♂）＝14,具有X－Y性别决定机制;减数分裂行为比较一致,但在中期－Ⅰ时,常染色体和性染色体的排列方式各不相同,可为蝽科昆虫的形态分类及系统发育提供有用的证据。二星蝽Eysarcoris guttiger(Thunberg）的染色体组成为2n（♂）＝15,具有X1X2Y性别决定机制,进一步证明了在半翅目昆虫的性染色体进化中碎片化过程起着很重要的作用;黑斑二星蝽Eysarcoris fabricii(Kirkaldy）的染色体组成为2n（♂）＝16,具有X－Y性别决定机制。后2种的核型结果,可为二星蝽属分类的进一步研究提供参考。     

黑腹蝽为害晚稻秧苗观察初报

<正> 黑腹蝽(广二星蝽,二小星蝽)Stollia ven-tralis(Westwood)属半翅目,蝽科,是我国常见的农作物害虫,除为害水稻外,还为害高粱、玉米、小米和豆类、棉花等多种作物。最近两年,我们在广东省四会县大沙公社发现此虫严重为     

四种蝽科昆虫的染色体研究

研究了4种中国蝽科昆虫的核型和染色体的减数分裂行为, 并首次在半翅目中采用核型分析软件对第一次减数分裂中期的染色体进行核型分析。结果表明: 4个种均为2n=14和X-Y性别决定机制; 减数分裂行为比较一致, 但在中期 I 常染色体和性染色体的排列方式各不相同; 核型分析后的结果表现出了种的特异性, 可为蝽科昆虫的形态分类及系统发育提供有用的证据。     

六种蝽象的染色体研究（半翅目：蝽科）

研究了6种蝽象的核型和减数分裂行为。结果表明：6个种的染色体组成均为2n(♂)=14, 具有X-Y性别决定机制;减数分裂行为比较一致,但在中期-Ⅰ常染色体和性染色体的排列方式具有种的特异性,可为蝽科昆虫的形态分类及系统发育提供有用的证据。     

蝽科昆虫精巢形态及属种间亲缘关系

为探讨蝽科精巢形态差异,以及据此反映的属种间亲缘关系,对蝽科9属13种昆虫精巢进行了观察和比较研究.结果表明,蝽科精巢形态在属内种间具有相对稳定性,属间、亚科间具有差异性.蝽科输精管种间变异大.基于精巢长度、宽度、面积及长宽比的聚类分析结果显示,斑须蝽属Dolycoris、绿蝽属Nezara、茶翅蝽属Halyomorpha关系较近,并与二星蝽属Eysarcoris形成并列关系.菜蝽属Eurydema、麦蝽属Aelia、珠蝽属Rubiconia亲缘关系密切.而果蝽属Carpocoris与条蝽属Graphosoma形成不同分支的特殊进化关系.因此,蝽科精巢可作为属级、亚科级的形态和数值分类特征.     

三种辉蝽的核型研究（半翅目：蝽科）

本首次研究了采于中国的辉蝽属三个种一辉蝽（Carbula obtusangula Reuter)、北方辉蝽（Carbula putoni(Jakovlev),凹肩辉蝽（Carbula sinica Hsiao et Cheng)的核型,结果表明,三个种均具有典型的蝽科核型即：2n(♂）＝14,具有XY性别决定机制,但是三个种的常染色体和性染色体在减数分裂时期的行为以及核型分析的结果和模式图各不相同,而且在北方辉蝽中出现了1－2条超数染色体,这些特点可为辉蝽属昆虫的形态分类及系统发育提供有用的证据。     

红角辉蝽和紫翅果蝽线粒体完整基因组测序及蝽亚科系统发育分析(半翅目: 蝽科)(英文)

【目的】本研究对红角辉蝽Carbula crassiventris和紫翅果蝽Carpocoris purpureipennis完整线粒体基因组测序,以探究蝽亚科(Pentatominae)线粒体基因组特征并重建其系统发育关系。【方法】使用Illumina MiSeq测序平台测定红角辉蝽和紫翅果蝽线粒体基因组全序列,并进行组装和注释。基于这2个种和其他30个蝽亚科分类单元线粒体基因组的13个蛋白质编码基因的第1和2位密码子以及2个rRNA基因的核苷酸序列,利用贝叶斯和最大似然法重建蝽亚科系统发育树。【结果】红角辉蝽和紫翅果蝽的线粒体基因组全长分别为15 824 和16 575 bp, 包含13个蛋白质编码基因、2个rRNA基因、22个tRNA基因和1个控制区。蝽亚科内线粒体基因组基因排列顺序保守且没有发现基因重排。此外,蝽亚科内的碱基组成、密码子使用和RNA结构均较为保守; 控制区重复序列拥有不同的长度、类型和拷贝数。基于贝叶斯法和最大似然法重建的系统发育树显示二星蝽族(Eysarcorini)、果蝽族(Carpocorini)、稻绿蝽族(Nezarini)和Antestiini构成一个稳定分枝。【结论】系统发育分析支持辉蝽属Carbula应属于二星蝽族,而果蝽属Carpocoris、斑须蝽属Dolycoris和珠蝽属Rubiconia同属于果蝽族。     

基于几何形态学的北二星蝽种内形态差异分析(半翅目:蝽科)（英文）

【目的】北二星蝽Eysarcoris aeneus是一种广泛分布于古北区的重要农业害虫,可危害多种经济作物。其刺肩型和钝肩型前胸背板后侧角长度存在差异,暗示其种内变异的存在。【方法】基于几何形态学的多元回归分析(multivariate regression)、主成分分析(principal component analysis,PCA)、典型变量分析(canonical variate analysis,CVA)和判别函数分析(discriminant function analysis,DFA),对采集于中国19个地区的142头标本(98头北二星蝽标本和44头作为外群的广二星蝽E. ventralis标本)的前翅、后翅、头和小盾片4个性状进行分析比较,研究北二星蝽钝肩型和刺肩型之间的形态变异。【结果】对于所研究的4个性状来说,北二星蝽钝肩型和刺肩型标本间均未检测到异速生长的存在。主成分分析中,钝肩型和刺肩型的标本均有重叠,典型变量分析则显示它们之间存在显著差异(马氏距离和普氏距离的P值均小于0. 01)。判别函数分析显示,依据这4个性状两型样本间的正确判别率在67%～89%之间。【结论】结果表明,前翅、后翅、头和小盾片都可以作为北二星蝽钝肩型和刺肩型之间形态变异的评价指标,小盾片特征具有最高水平的鉴别价值;对于所研究的这4个性状来说,北二星蝽钝肩型和刺肩型之间都表现出显著的形状差异,而它们的质心距离差异不显著,说明相对于体型大小差异分析,形状差异分析能更灵敏地揭示谱系间的变异。本研究表明几何形态学可以有效地描述北二星蝽的种内形态变异,为蝽类昆虫种内变异的研究奠定了基础。     

Telomeres act autonomously in maize to organize the meiotic bouquet from a semipolarized chromosome orientation

During meiosis, chromosomes undergo large-scale reorganization to allow pairing between homologues, which is necessary for recombination and segregation. In many organisms, pairing of homologous chromosomes is accompanied, and possibly facilitated, by the bouquet, the clustering of telomeres in a small region of the nuclear periphery. Taking advantage of the cytological accessibility of meiosis in maize, we have characterized the organization of centromeres and telomeres throughout meiotic prophase. Our results demonstrate that meiotic centromeres are polarized prior to the bouquet stage, but that this polarization does not contribute to bouquet formation. By examining telocentric and ring chromosomes, we have tested the cis-acting requirements for participation in the bouquet. We find that: (a) the healed ends of broken chromosomes, which contain telomere repeats, can enter the bouquet; (b) ring chromosomes enter the bouquet, indicating that terminal position on a chromosome is not necessary for telomere sequences to localize to the bouquet; and (c) beginning at zygotene, the behavior of telomeres is dominant over any centromere-mediated chromosome behavior. The results of this study indicate that specific chromosome regions are acted upon to determine the organization of meiotic chromosomes, enabling the bouquet to form despite large-scale changes in chromosome architecture.     

Mutations that affect meiosis in male mice influence the dynamics of the mid-preleptotene and bouquet stages

Meiosis pairs and segregates homologous chromosomes and thereby forms haploid germ cells to compensate the genome doubling at fertilization. Homologue pairing in many eukaryotic species depends on formation of DNA double strand breaks (DSBs) during early prophase I when telomeres begin to cluster at the nuclear periphery (bouquet stage). By fluorescence in situ hybridization criteria, we observe that mid-preleptotene and bouquet stage frequencies are altered in male mice deficient for proteins required for recombination, ubiquitin conjugation and telomere length control. The generally low frequencies of mid-preleptotene spermatocytes were significantly increased in male mice lacking recombination proteins SPO11, MEI1, MLH1, KU80, ubiquitin conjugating enzyme HR6B, and in mice with only one copy of the telomere length regulator Terf1. The bouquet stage was significantly enriched in Atm(-/-), Spo11(-/-), Mei1(m1Jcs/m1Jcs), Mlh1(-/-), Terf1(+/-) and Hr6b(-/-) spermatogenesis, but not in mice lacking recombination proteins DMC1 and HOP2, the non-homologous end-joining DNA repair factor KU80 and the ATM downstream effector GADD45a. Mice defective in spermiogenesis (Tnp1(-/-), Gmcl1(-/-), Asm(-/-)) showed wild-type mid-preleptotene and bouquet frequencies. A low frequency of bouquet spermatocytes in Spo11(-/-)Atm(-/-) spermatogenesis suggests that DSBs contribute to the Atm(-/-)-correlated bouquet stage exit defect. Insignificant changes of bouquet frequencies in mice with defects in early stages of DSB repair (Dmc1(-/-), Hop2(-/-)) suggest that there is an ATM-specific influence on bouquet stage duration. Altogether, it appears that several pathways influence telomere dynamics in mammalian meiosis.     

中国新疆地区粉虱种类（半翅目：粉虱科）记述

记述了新疆地区粉虱5属6种,即欧洲甘蓝粉虱Aleyrodes proletella(Linnaeus),葡萄穴粉虱Aleurolobus shantungi Tang,非洲小粉虱Bemisia afer(PriesnerHosny),烟粉虱Bemisia tabaci(Gennadius),桑粉虱Pealius mori(Takahashi),温室白粉虱Trialeurodes vaporariorum(Westwood),其中葡萄穴粉虱为新疆新记录种。并且用扫描电镜对其伪蛹进行拍照,并依据玻片标本进行了描述。编制了新疆地区粉虱分类检索表。     

Modeling meiotic chromosomes indicates a size dependent contribution of telomere clustering and chromosome rigidity to homologue juxtaposition

Meiosis is the cell division that halves the genetic component of diploid cells to form gametes or spores. To achieve this, meiotic cells undergo a radical spatial reorganisation of chromosomes. This reorganisation is a prerequisite for the pairing of parental homologous chromosomes and the reductional division, which halves the number of chromosomes in daughter cells. Of particular note is the change from a centromere clustered layout (Rabl configuration) to a telomere clustered conformation (bouquet stage). The contribution of the bouquet structure to homologous chromosome pairing is uncertain. We have developed a new in silico model to represent the chromosomes of Saccharomyces cerevisiae in space, based on a worm-like chain model constrained by attachment to the nuclear envelope and clustering forces. We have asked how these constraints could influence chromosome layout, with particular regard to the juxtaposition of homologous chromosomes and potential nonallelic, ectopic, interactions. The data support the view that the bouquet may be sufficient to bring short chromosomes together, but the contribution to long chromosomes is less. We also find that persistence length is critical to how much influence the bouquet structure could have, both on pairing of homologues and avoiding contacts with heterologues. This work represents an important development in computer modeling of chromosomes, and suggests new explanations for why elucidating the functional significance of the bouquet by genetics has been so difficult.     

REVISION OF CHINESE SPECIES OF HEMIPTARSENUS WESTWOOD (HYMENOPTERA: EULOPHIDAE) *

Abstract This paper deals with Chinese species of Hemiptarsenus Westwood, 1833. Totally five species are found in China. Among them, H. unguicellus (Zetterstedt), H. ornatus (Nees) and H. varicornis (Gi‐rault) were previously recorded, H. zilahisebessi Erdös is newly recorded in China and H. strigiscuta sp. n. is described as new. A tentative key to known species is given, and other three external species, H. fulvicollis Westwood, H. wailesellae Nowicky and H. waterhousii Westwood, are included in the key for comparison. The type specimen is deposited in the Zoological Museum, Institute of Zoology, Chinese Academy of Sciences.     

Directed motion of telomeres in the formation of the meiotic bouquet revealed by time course and simulation analysis

Chromosome movement is critical for homologous chromosome pairing during meiosis. A prominent and nearly universal meiotic chromosome reorganization is the formation of the bouquet, characterized by the close clustering of chromosome ends at the nuclear envelope. We have used a novel method of in vitro culture of rye anthers combined with fluorescent in situ hybridization (FISH) detection of telomeres to quantitatively study bouquet formation. The three-dimensional distribution of telomeres over time was used to obtain a quantitative profile of bouquet formation intermediates. The bouquet formed through a gradual, continuous tightening of telomeres over approximately 6 h. To determine whether the motion of chromosomes was random or directed, we developed a computer simulation of bouquet formation to compare with our observations. We varied the diffusion rate of telomeres and the amount of directional bias in telomere movement. In our models, the bouquet was formed in a manner comparable to what we observed in cultured meiocytes only when the movement of telomeres was actively directed toward the bouquet site, whereas a wide range of diffusion rates were permitted. Directed motion, as opposed to random diffusion, was required to reproduce our observations, implying that an active process moves chromosomes to cause telomere clustering.     

Morphology and ultrastructure of the germarium in panoistic ovarioles of a basal “apterygotous” insect,Thermobia domestica

It has been shown that in Drosophila the germline stem cells (GSCs), similar to the germline and non-germline stem cells of other species, develop and function in specialized microenvironments formed by somatic cells, referred to as the niches. In the fruit fly ovaries, the female GSCs divide asymmetrically to produce new GSCs and the progenitor cells, the cystoblasts (Cbs). Each Cb then divides to generate the cyst composed of 16 interconnected sibling cells, the cystocytes. After cyst formation, specific molecules are transferred to one of the cystocytes which differentiates into the oocyte, whereas the other 15 cystocytes become the nurse cells. We have studied morphology and ultrastructure of the germaria in the ovarioles (ovaries) of a basal “apterygotous” insect, the firebrat (Thermobia domestica). Our analyses have revealed that in this insect, putative GSCs are present along the anterior apex of the germarium. These cells are separated from each other and from the basement lamina covering the ovariole by characteristic somatic cells, termed the apical somatic cells (ASCs), or their elongated processes. We believe that all the ASCs of a given ovariole constitute a “dispersed” niche in which putative GSCs are anchored. Our analyses have additionally shown that in Thermobia, both the Cbs and young (meiotic) oocytes are always individual and never form syncytial cysts. These findings indicate that in certain basal insects the syncytial phase of oogenesis has been eliminated during evolution. Finally, we show that in the early meiotic oocytes of Thermobia, during the so-called bouquet stage, prominent Balbiani bodies (Bbs) are formed. Analysis of serial micrographs indicates that the Bbs invariably arise next to the segment of the nuclear envelope to which the telomeres of the bouquet chromosomes are attached. We suggest, in the light of these data, that the localization of the Bb together with the polar attachment of the bouquet chromosomes play a crucial role in the early asymmetrization of Thermobia oocytes.     

Centromeres Cluster De Novo at the Beginning of Meiosis in Brachypodium distachyon

In most eukaryotes that have been studied, the telomeres cluster into a bouquet early in meiosis, and in wheat and its relatives and in Arabidopsis the centromeres pair at the same time. In Arabidopsis, the telomeres do not cluster as a typical telomere bouquet on the nuclear membrane but are associated with the nucleolus both somatically and at the onset of meiosis. We therefore assessed whether Brachypodium distachyon, a monocot species related to cereals and whose genome is approximately twice the size of Arabidopsis thaliana, also exhibited an atypical telomere bouquet and centromere pairing. In order to investigate the occurrence of a bouquet and centromere pairing in B distachyon, we first had to establish protocols for studying meiosis in this species. This enabled us to visualize chromosome behaviour in meiocytes derived from young B distachyon spikelets in three-dimensions by fluorescent in situ hybridization (FISH), and accurately to stage meiosis based on chromatin morphology in relation to spikelet size and the timing of sample collection. Surprisingly, this study revealed that the centromeres clustered as a single site at the same time as the telomeres also formed a bouquet or single cluster.     

A revision of Neomegalotomus (Hemiptera: Alydidae)

We recognize two species in Neomegalotomus, N. parvus (Westwood), the type species; and N. rufipes (Westwood). The two species are redescribed from type specimens, and are keyed. We synonymize the following species with Neomegalotomus parvus: N. simplex (Westwood), N. latifascia (Berg), and N. pallescens (St?l) (all new synonymies). We synonymize N. jamaicensis (Westwood) with N. rufipes (new synonymy). The type specimens of all species hitherto placed in the genus are also redescribed, except those of N. debilis (Walker) and N. vicinus (Westwood). N. parvus occurs from México through Central America into northern Argentina and east into Venezuela and adjacent Caribbean islands. N. rufipes is widespread in the Caribbean south towards Venezuela. The two species overlap in distribution: N. parvus is found on St. Vincent and Tobago, whereas N. rufipes occurs on Grenada, which lies between those two islands.     

Homolog pairing and two kinds of bouquets in the meiotic prophase of rye,Secale cereale

Chromosome configurations and structures during meiotic prophase were investigated by staining large repeated DNA sequences localized in the subtelomeric regions of all the chromosomes in rye, Secale cereale, in order to clarify when and how homolog pairing and bouquet formation occur. The changes of the spatial locations of chromosomes in the nucleus were investigated by the use of laser confocal microscopy, together with the surface-spreading method of silver nitrate staining to detect the formation of the synaptonemal complex. Homolog pairing in which homologs of four chromatids of a pair of homologs were coaligned in parallel but remained distinctly separate was microscopically detected for the first time in the present study. Homolog pairing showed the following characteristics: (1) it occurred at the leptotene-zygotene transition stage, prior to the formation of nodules and the synaptonemal complex; (2) the chromatin structure of chromosomes was in a state of decondensation; (3) it required no telomere clustering. These data suggest that homolog pairing represents a structure that indicates incipient recombination. After the homolog pairing stage, two kinds of bouquet configuration were found in zygotene. The commonly observed type was a loose bouquet, in which the subtelomeric regions were loosely aggregated. The other type was a definite bouquet, in which almost all the subtelomeric regions were conjugated, but this type was observed only in a limited number of the meiotic prophase cells of some individuals. It was concluded that the former represents the configuration of homologous recombination and the latter that of ectopic recombination.