梧桐科分类学研究评述

梧桐科(Sterculiaceae)是锦葵目中的一个多型科,主要分布于热带和亚热带地区,只有少数种可分布到温带地区。由于该科植物的形态特征较为多样化,至今对于它的范围和所包含的属种数目在各国学者间仍没有达成共识。该文从梧桐科的分类地位和系统关系、属的分类地位和亲缘关系以及分类学新特征在梧桐科分类中的应用3个方面入手,分析了梧桐科分类学研究的历史、现状和存在的问题,特别是把来自分子资料的研究结果与传统分类进行了比较分析,试图为梧桐科的分类学研究提供更多的帮助。     

9种梧桐科植物叶表皮特征的扫描电镜研究

用扫描电镜对9种梧桐科植物叶片进行观察研究以明确其叶表皮微形态特征差异.结果显示,绝大部分梧桐科植物的气孔类型和气孔形状相似,但其表皮的毛状体类型、形态以及表皮纹饰等方面有显著差异.结果表明9种梧桐科植物的叶表皮毛和表皮纹饰可作为梧桐科种间分类的特征,且研究结果支持将胖大海归属于胖大海属,将翅子树单独列为翅子树族的分类观点.     

基于线粒体16S rDNA基因的天牛科部分种类分子系统学研究(鞘翅目:天牛科)

研究测定了天牛科3亚科9种昆虫线粒体16S rDNA基因约500bp的序列,对序列的碱基组成和遗传距离进行分析。并基于16S rDNA基因序列数据,采用邻接法(NJ)和最大简约法(MP)分析天牛科3亚科分子系统发育关系。研究结果表明,2种方法得到的分子系统树其分支结果一致,可将内群分为2个分支,第1个分支包括沟胫天牛亚科和天牛亚科;第2个分支包括花天牛亚科。16SrDNA基因对天牛科亚科间系统发育的研究是有价值的。     

基于叶绿体基因组数据的芸香科属间系统发育初步分析

为探究花椒属种水平系统进化关系以及为新品种培育研究奠定理论基础，该研究以芸香科物种的叶片为材料，采用改良CTAB法提取叶绿体DNA,利用BGISEQ-500平台进行叶绿体基因组测序，并对叶绿体基因组进行组装、注释，联合NCBI数据库数据，共获得芸香科19属49个物种的全叶绿体基因组序列。构建了芸香科属间系统进化关系。结果表明，(1)基于叶绿体基因组序列矩阵(总长196 641 bp),ML和BI 2种方法得到的系统发育树的拓扑结够基本一致，系统发育树各分支具有较强的支持率，叶绿体基因组数据可以解决芸香科属间的系统发育关系。(2)芸香科为单系类群，并进一步形成两大分支，其中柑橘亚科为单系，与芸香亚科内的芸香属聚为分支I,分支Ⅱ由芸香亚科和飞龙掌血亚科组成，两亚科均不是单系，其中飞龙掌血亚科的香肉果属，茵芋属与芸香亚科的白鲜属，臭常山属是最早分化出来的类群，其次是蜜茱萸属和山油柑属；黄檗属和吴茱萸属与花椒属类群形成姊妹群，飞龙掌血属的物种飞龙掌血嵌套于花椒属分支中，支持飞龙掌血物种并入花椒属的处理。     

中国锦葵科一新记录种——克氏梧桐

首次报道中国锦葵科一新记录种——克氏梧桐［Firmiana kerrii (Craib) Kosterm.］。该种原记载产自泰国和缅甸,2019年该种在中国云南西双版纳州勐腊县发现有分布。凭证标本保存在中国科学院西双版纳热带植物园标本馆(HITBC)。该文给出了中国已知的9种梧桐属植物的分种检索表。     

梧桐科一些属的分类位置探讨

梧桐科（Ｓｔｅｒｃｕｌｉａｃｅａｅ）是锦葵目中的一个多型科,科的特征比较比样化。自从Ｅ．Ｐ．Ｖｅｎｔｅｎａｔ（１８３０）建立该科以来,对于该科范围和包含的属种数目,各国学者至今尚存在各种不同的看法。作者认为,火桐属（Ｅｒｙｔｈｒｏｐｓｉｓ）应当从梧桐属（Ｆｉｒｍｉａｎａ）中分出成为单独的属;午时花属（Ｐｅｎｔａｐｅｔｅｓ）不应归入锦葵科（Ｍａｌｖａｃｅａｅ）,应当置于梧桐科;田麻属（Ｃｏｒｃｈｏｒ     

基于线粒体COⅡ基因的中国蝽科分子系统学研究(半翅目,异翅亚目)

扩增并测定了我国蝽科4亚科8属11种昆虫线粒体COⅡ基因585 bp的序列,对序列的碱基组成、转换颠换、遗传距离等进行分析,探讨了COⅡ基因在该科的分子进化机制.并基于COⅡ基因序列数据,分别采用邻接法(NI)、最大简约法(MP)和贝叶斯推论法(BI)建立蝽科分子系统发育关系.研究结果表明,蝽科昆虫COⅡ基因A T含量平均为71.7%,存在较强的A T含量偏向性,氨基酸的变异率为27.2%;亚科间的遗传距离介于0.168～0.242之间,大于亚科内属种间的遗传距离,蝽科与盾蝽科2外群之间遗传距离最大,两科之间存在明显的间断.分子系统发育树表明,短喙蝽亚科为蝽科中较为原始的类群,分化较早,益蝽亚科与舌盾蝽亚科关系较近,形成一对姐妹群,蝽科中捕食性种类--益蝽亚科是较为特化的类群,它是由植食性种类分化而来.蝽科4亚科间的分子系统发育关系为Phyllocephalinae (Pentatominae (Asopinae Podopinae).     

基于内转录间隔区基因片段对叩甲科昆虫的系统发育研究

【目的】采用叩甲科昆虫的内转录间隔区(ITS-2)片段对叩甲科昆虫部分种类进行系统发育分析,明确各亚科类群间的亲缘关系并同传统分类系统进行比较,验证ITS-2片段是否能用于叩甲科昆虫的分子系统学研究。【方法】基于叩甲科昆虫的内转录间隔区(ITS-2)片段,对10个亚科69个种类的叩甲进行了系统发育分析。进行系统发育信号检测,计算各亚科之间的遗传距离,采用邻接法、似然法和简约法三种模型构建系统发育树。【结果】3种方法构建系统发育树结构基本一致,各亚科都能被很好的聚类,且各亚科间遗传距离符合传统分类学观点。同时,分析结果也支持对传统分类系统进行修改:尖鞘叩甲亚科Oxynopterinae和异角叩甲亚科Pityobiinae被聚入齿胸叩甲亚科Denticollinae,建议将尖鞘叩甲亚科和异角叩甲亚科同齿胸叩甲亚科合并;槽缝叩甲亚科Agrypninae和单叶叩甲亚科Conoderinae并入萤叩甲亚科Pyrophorinae;梳爪叩甲类群Melanotinae被聚类到叩甲亚科Elaterinae内,建议将梳爪叩甲亚科并入叩甲亚科。【结论】分析结果显示,ITS-2片段适用于叩甲科昆虫低级分类阶元的系统发育分析,各亚科之间的亲缘关系符合传统的分类学观点,但聚类结果也有同传统分类系统有所不同,可为分类系统的修改提供依据。     

利用低拷贝核基因重建菊科紫菀亚科族间系统发育关系

紫菀亚科(Asteroideae)是菊科最大的一个亚科, 包含的种数多于被子植物的绝大多数科。目前, 紫菀亚科族间的系统发育关系主要依赖于叶绿体基因信息, 但是叶绿体基因为单亲遗传, 并不能完整反映进化历史。鉴于杂交现象在菊科普遍存在, 故利用核基因可以反映更完整的紫菀亚科进化历史。该研究首次使用从转录组数据(20个新测+11个从NCBI数据库下载)中筛选出的47个直系同源低拷贝核基因来研究紫菀亚科的系统发育关系, 共选取了29个物种, 代表了紫菀亚科20个族中的13个族。用超矩阵分析方法和溯祖推测分析方法各获得了1个稳定的紫菀亚科系统树, 每个树上绝大多数分支都得到了高度支持, 且2个树之间没有明显的冲突。新的紫菀亚科族间系统发育关系揭示了千里光超族应并入紫菀超族, 春黄菊族可能是千里光族与紫菀族杂交起源的, 金鸡菊族很可能也是杂交起源的。该研究结果显示低拷贝核基因可以更好地解决科以下分类阶元的系统发育关系, 对菊科乃至被子植物其它科的系统发育研究具有重要的借鉴意义。     

两种毛蚜线粒体基因组比较分析

【目的】线粒体基因组分析已被应用于昆虫系统发育研究。本研究以蚜科Aphididae重要类群毛蚜亚科物种为代表,测定并比较分析了该类蚜虫的线粒体基因组特征,探讨了基于线粒体基因组信息的蚜虫系统发育关系重建。【方法】以毛蚜亚科三角枫多态毛蚜Periphyllus acerihabitans Zhang和针茅小毛蚜Chaetosiphella stipae Hille Ris Lambers,1947为研究对象,利用长短PCR相结合的方法测定线粒体基因组的序列,分析了基因组的基本特征;基于在线t RNAscan-SE Search Server搜索方法预测了t RNA的二级结构;基于12个物种(本研究获得的2个物种和10个Gen Bank上下载的物种数据)的蛋白编码基因(PCGs)序列,利用最大似然法和贝叶斯法重建了蚜科的系统发育关系。【结果】两种毛蚜均获得了约94%的线粒体基因组数据,P.acerihabitans获得了14 908 bp,控制区为1 205 bp;C.stipae获得了13 893 bp,控制区为609 bp。两种毛蚜同时获得33个基因,包含接近完整的13个蛋白编码基因(PCGs)(nad5不完整),18个tRNA,2个rRNA基因;ka/ks值表明,C.stipae的进化速率更快。从基因组组成、基因排列顺序、核苷酸组成分析、密码子使用情况、t RNA二级结构等特征来分析,两种蚜虫线粒体基因组基本特征相似。系统发育重建结果表明毛蚜亚科、蚜亚科的单系性得到了支持,毛蚜亚科位于蚜科的基部位置。【结论】两种毛蚜线粒体基因组的基本特征相似,符合蚜虫线粒体基因组的一般特征,两种线粒体基因组的长度差异主要来自控制区长度的不同;系统发育重建支持毛蚜亚科与蚜亚科的单系性,毛蚜亚科位于蚜科较为基部的位置。研究结果为蚜虫类系统发育重建提供了参考。     

Phylogenetic analysis of the Malvadendrina clade (Malvaceae s.l.) based on plastid DNA sequences

Phylogenetic relationships within Malvaceae s.l., a clade that includes the traditional families Bombacaceae, Malvaceae s.str., Sterculiaceae, and Tiliaceae, have become greatly clarified thanks to recent molecular systematic research. In this paper, we use DNA sequences of four plastid regions (atpB, matK, ndhF, and rbcL) to study relationships within Malvadendrina, one of the two major clades of Malvaceae s.l. The four data sets were generally in agreement, but five terminal taxa manifested highly unexpected affinities in the rbcL partition, and the non-coding sequences of the trnK intron were found to provide limited phylogenetic information for resolving relationships at the base of Malvadendrina. The remaining data strongly support the existence of six major clades within Malvadendrina: Brownlowioideae, Dombeyoideae, Helicteroideae, Malvatheca (comprising Bombacoideae and Malvoideae), Sterculioideae, and Tilioideae. These data also resolve the placement of two problematic taxa: Nesogordonia (in Dombeyoideae) and Mortoniodendron (in Tilioideae). The relationships among the six clades are not definitively resolved, but the best-supported topology has Dombeyoideae as sister to the remainder of Malvadendrina (posterior probability PP=80%) and Sterculioideae as sister to Malvatheca (PP=86%). This early branching position of Dombeyoideae is supported by similarities in floral characters between members of that clade and outgroup taxa in Byttnerioideae. Similarly, the sister-group relationship of Sterculioideae and Malvatheca receives support from androecial characteristics, like subsessile or sessile anthers and an absence of staminodes, shared by these two clades.     

质体系统发育基因组解析旋花科系统发育关系

旋花科是一个世界广布的类群,具有丰富的形态特征和重要的经济价值。然而,目前该科主要分支或族间的系统发育关系问题一直未解决。为解析旋花科内系统发育关系,该研究代表性选取旋花科内8个族40个物种,基于质体全基因组数据,使用最大似然法和贝叶斯推论进行系统发育分析。结果表明:(1)旋花科质体基因组均为四分体结构,质体基因组大小为113 273～164 112 bp,蛋白质编码基因数目为66～79个。(2)基于五种DNA矩阵(即WCG、CDS、LSC、IR、SSC)的系统发育分析结果显示,WCG矩阵和CDS矩阵的拓扑结构基本一致,仅少数分支的支持率略有差异; LSC矩阵和WCG矩阵的拓扑结构差异在于菟丝子族、马蹄金族和盐帚花族的系统位置; AU检验和SH检验结果显示,WCG矩阵和SSC矩阵与IR矩阵的拓扑结构有显著冲突。(3)所有系统发育分析结果均显示,菟丝子属和马蹄金族都包括在旋花亚科内,应处理为族等级。(4)基于WCG矩阵和CDS矩阵较好地解决了旋花科8个族之间的系统发育关系,即心被藤族和丁公藤族聚为一支,最先从旋花亚科分化出来,随后是菟丝子族,剩下的5个族分成2个分支。(5)系统发育基因组分析证实,由于鱼黄草族特别是鱼黄草属是一个多系类群,因此需重新修订该族的分类地位和鱼黄草属的划分。     

DNA sequence data reveal polyphyly of Brexioideae (Brexiaceae; Saxifragaceae sensu lato)

Previous molecular phylogenetic analyses have demonstrated that Saxifragaceae sensu lato are polyphyletic, with component lineages scattered throughout the eudicots. As part of our effort to elucidate the relationships of members of Engler and Prantl's Saxifragaceae s. l., we undertook a molecular systematic study of subfamily Brexioideae, which comprises three genera:Brexia, Ixerba, andRoussea. Not all taxonomic treatments have concurred, however, in placing these genera together. To elucidate relationships among these three genera as well as their relationships to other angiosperms we constructed large data sets ofrbcL, 18S rDNA, andrbcL + 18S rDNA sequences. Our phylogenetic analyses indicate clearly that Brexioideae are polyphyletic.Brexia is part of a celastroid clade that also includesParnassia, Lepuropetalon, and Celastraceae.Ixerba appears as sister to a large eurosid I clade;Roussea appears as part of Asterales. Molecular data, therefore, indicate that Brexioideae are a polyphyletic assemblage and component genera should ultimately be incorporated into other groups. Our studies continue to demonstrate the polyphyly not only Saxifragaceae s. l., but also of its constituent subfamilies.The first author would like to dedicate this paper to Kurt Schuchart, a good friend who passed away during this research.     

Los domacios de Mortoniodendron (Malvaceae s.l.)

We describe the domatia of nine species of the genus Mortoniodendron, based on observations of cleared leaves and scanning electron micrographs. We recognize four kinds of domatia in Mortoniodendron species: cryptpocket, crypt, pocket and tufts of hairs, mostly associated with primary, secondary and tertiary veins. Mortoniodendron anisophyllum and M. costaricense have domatia up to the tertiary and quaternary veins. Moreover, domatia are absent in only two species, M. pentagonum and M. uxpanapense. Although there are reports on the occurrence of domatia in Malvaceae s.l., mainly in Brownlowioideae, Sterculioideae, and Tilioideae subfamilies, they are poorly described, and based on the different types of domatia found in Mortoniodendron we suggest reviewing other genera to better describe the diversity of domatia in Malvaceae s.l.

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Resumen  Se describen los domacios presentes en nueve especies del género Mortoniodendron utilizando la técnica de diafanización y el microscopio electrónico de barrido. En el género se observaron cuatro tipos de domacios: criptabolsa, cripta, bolsa y mechón de tricomas, la mayoría asociados a las venas primaria, secundarias y terciarias. Mortoniodendron anisophyllum y M. costaricense tienen domacios hasta las bifurcaciones de venas terciarias y cuaternarias. únicamente en dos especies, M. pentagonum y M. uxpanapense, los domacios están ausentes. A pesar de que se han registrado domacios en miembros de Malvaceae s.l., predominantemente en las subfamilias Brownlowioideae, Sterculioideae y Tilioideae; pocas veces se describe su tipo. Por ello, con base en los diferentes tipos de domacios encontrados en Mortoniodendron sugerimos estudiar otros géneros y confirmar la diversidad en Malvaceae s.l.

     

The phylogeny of leaf beetles (Chrysomelidae) inferred from mitochondrial genomes

The high-level classification of Chrysomelidae (leaf beetles) currently recognizes 12 or 13 well-established subfamilies, but the phylogenetic relationships among them remain ambiguous. Full mitochondrial genomes were newly generated for 27 taxa and combined with existing GenBank data to provide a dataset of 108 mitochondrial genomes covering all subfamilies. Phylogenetic analysis under maximum likelihood and Bayesian inference recovered the monophyly of all subfamilies, except that Timarcha was split from Chrysomelinae in some analyses. Three previously recognized major clades of Chrysomelidae were broadly supported: the ‘chrysomeline’ clade consisting of (Chrysomelinae (Galerucinae + Alticinae)); the ‘sagrine’ clade with internal relationships of ((Bruchinae + Sagrinae) + (Criocerinae + Donaciinae)), and the ‘eumolpine’ clade comprising (Spilopyrinae (Cassidinae (Eumolpinae (Cryptocephalinae + Lamprosomatinae)))). Relationships among these clades differed between data treatments and phylogenetic algorithms, and were complicated by two additional deep lineages, Timarcha and Synetinae. Various topological tests favoured the PhyloBayes software as the preferred inference method, resulting in the arrangement of (chrysomelines (eumolpines + sagrines)), with Timarcha placed as sister to the chrysomeline clade and Synetinae as a deep lineage splitting near the base. Whereas mitogenomes provide a solid framework for the phylogeny of Chrysomelidae, the basal relationships do not agree with the topology of existing molecular studies and remain one of the most difficult problems of Chrysomelidae phylogenetics.     

猴欢喜叶绿体全基因组及杜英科系统地位分析

最新的分子系统发育(APG IV)研究中以猴欢喜属(Sloanea L.)为代表的杜英科(Elaeocarpaceae)所在的酢浆草目(Oxalidales)被置于豆类分支(Fabids),且与卫矛目(Celastrales)、金虎尾目(Malpighiales)组成一支(COM分支),但支持率较低.为提高COM分支支...     

Support for an expanded family concept of Malvaceae within a recircumscribed order Mai vales: a combined analysis of plastid atpB and rbcL DNA sequences

Sequence analyses of the plastid genes atpB and rbcL support an expanded order Malvales. Within this alliance, core Malvales are clearly supported and comprise most genera that have previously been included in Sterculiaceae, Tiliaceae, Bombacaceae, and Malvaceae. Additional well supported malvalean alliances include the bixalean clade (Bixaceae, Diego-dendraceae, and Cochlospermaceae), the cistalean clade (Cistaceae, Dipterocarpaceae, and Sarcolaenaceae) and Thymelaeaceae (including Gonystyloideae and Aquilarioideae). Our results indicate sister-group relationships between (1) Neuradaceae and the cistalean clade; (2) Sphaerosepalaceae and Thymelaeaceae; (3) these two clades (1 and 2); and (4) all these and an alliance comprising the bixalean clade and core Malvales, but this pattern is weakly supported by the bootstrap. The affinities of Muntingiaceae and Petenaea are especially ambiguous, although almost certainly they are Malvales s.l. The traditional delimitation of families within core Malvales is untenable. Instead, we propose to merge Sterculiaceae, Tiliaceae and Bombacaceae with Malvaceae and subdivide this enlarged family Malvaceae into nine subfamilies based on molecular, morphological, and biogeographical data: (1) Byttnerioideae, including tribes Byttnerieae, Lasiopetaleae and Theobromeae (all of which have cucullate petals) and Hermannieae; (2) Grewioideae, including most genera of former Tiliaceae; (3) Tilioideae, monogeneric in our analysis; (4) Helicteroideae, comprising most of the taxa previously included in Helictereae, plus Mansonia, Triplochiton (indicating that apocarpy evolved at least twice within Malvaceae) and possibly Durioneae; (5) Sterculioideae, defined by apetalous, apocarpous, usually unisexual flowers with androgynophores; (6) Brownlowioideae, circumscribed as in previous classifications; (7) Dombeyoideae, expanded to include Burretiodendron, Eriolaena, Pterospermum, and Schoutmia; (8) Bombacoideae, corresponding to former Bombacaceae (without Durioneae) but including Fremontodendreae     

The earliest record of the genus Cola (Malvaceae sensu lato: Sterculioideae) from the Late Oligocene (28–27 Ma) of Ethiopia and leaf characteristics within the genus

A fossil leaf compression from the Late Oligocene (28–27 Ma) of northwestern Ethiopia is the earliest record of the African endemic moist tropical forest genus Cola (Malvaceae sensu lato: Sterculioideae). Based on leaf and epidermal morphology, the fossil is considered to be very similar to two extant Guineo-Congolian species but differences warrant designation of a new species. This study also includes a review of the fossil record of Cola, a comprehensive summary of leaf characteristics within several extant species of Cola, Octolobus, and Pterygota, and a brief discussion of the paleogeographic implications of the fossil species affinity and occurrence in Ethiopia.     

Non-monophyly of the woody bamboos (Bambuseae; Poaceae): a multi-gene region phylogenetic analysis of Bambusoideae s.s.

The taxonomy of Bambusoideae is in a state of flux and phylogenetic studies are required to help resolve systematic issues. Over 60 taxa, representing all subtribes of Bambuseae and related non-bambusoid grasses were sampled. A combined analysis of five plastid DNA regions, trnL intron, trnL-F intergenic spacer, atpB-rbcL intergenic spacer, rps16 intron, and matK, was used to study the phylogenetic relationships among the bamboos in general and the woody bamboos in particular. Within the BEP clade (Bambusoideae s.s., Ehrhartoideae, Pooideae), Pooideae were resolved as sister to Bambusoideae s.s. Tribe Bambuseae, the woody bamboos, as currently recognized were not monophyletic because Olyreae, the herbaceous bamboos, were sister to tropical Bambuseae. Temperate Bambuseae were sister to the group consisting of tropical Bambuseae and Olyreae. Thus, the temperate Bambuseae would be better treated as their own tribe Arundinarieae than as a subgroup of Bambuseae. Within the tropical Bambuseae, neotropical Bambuseae were sister to the palaeotropical and Austral Bambuseae. In addition, Melocanninae were found to be sister to the remaining palaeotropical and Austral Bambuseae. We discuss phylogenetic and morphological patterns of diversification and interpret them in a biogeographic context.