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An updated infrageneric classification based on phylogenomics and character evolution in Hydrangea (Hydrangeaceae) 基于系统发生组学和绣球花(绣球花科)特征进化的最新下属分类法
IF 3.4 2区 生物学 Q2 EVOLUTIONARY BIOLOGY Pub Date : 2024-03-22 DOI: 10.1002/tax.13158
Xudong Yang, Tiantian Xue, Tiangang Gao, Yunfen Liang, Erik F. Smets, Sudhindra R. Gadagkar, Shengxiang Yu
The genus Hydrangea s.l. (Hydrangeaceae), a favorite among gardeners, comprises more than 80 species that are important understory plants in natural temperate and subtropical forests of the Northern Hemisphere. These species are hypervariable in morphology, especially in indumentum and floral characters, warranting a thorough exploration of the complex evolutionary history of morphological characters of the genus. Ideally, this is done within a robust phylogenetic framework with extensive taxon sampling. In this study, we propose a comprehensive taxonomic reassessment of Hydrangea based on a reconstruction of its molecular phylogeny based mainly on the chloroplast genome (plastome) and the most representative taxon sampling reported to date. Phylogenomic reconstruction yielded five well‐resolved major clades and three newly recognized subclades. Inspection of the 28 characters employed in traditional taxonomic revisions revealed homoplasy in many of these traits. Our results show that characters such as growth habit, woody stem type, number of enlarged marginal sepals, style and stamen number, fruit shape, and ovary position are useful for circumscribing infrageneric divisions. Unique synapomorphies are limited. For example, herb and subshrub growth habits are associated with all the species in H. sect. Deinanthe and sect. Cardiandra, respectively. Character state combinations are proposed for distinguishing infrageneric taxa. Based on a robust phylogenetic framework, our findings suggest a complex evolutionary history of Hydrangea morphological characters. Following the criterion of monophyly and considering the morphological consistency and synapomorphy of single and combined characters to diagnose relevant lineages, we update the classification of Hydrangea into 5 subgenera and 19 sections. Our proposed taxonomic scheme, based on a robust phylogenetic framework and in‐depth character study, provides an updated perspective on the infrageneric subdivision of Hydrangea s.l.
绣球花属(Hydrangea s.l.)是园艺家的最爱,该属有 80 多个物种,是北半球天然温带和亚热带森林中重要的林下植物。这些物种在形态上,尤其是在毛被和花的特征上,存在很大的变异性,因此有必要对该属形态特征的复杂进化史进行深入研究。理想的情况是在一个强大的系统发育框架内,通过广泛的类群取样来完成这一工作。在本研究中,我们主要基于叶绿体基因组(质粒体)和迄今报道的最具代表性的类群取样,重建了绣球属的分子系统发育,并在此基础上对绣球属进行了全面的分类学重新评估。系统发生组的重建产生了五个清晰的主要支系和三个新确认的亚支系。对传统分类学修订中使用的 28 个特征进行检查后发现,其中许多特征存在同源性。我们的研究结果表明,生长习性、木质茎类型、扩大的边缘萼片数量、花柱和雄蕊数量、果实形状和子房位置等特征有助于划分下属。独特的同形异构体是有限的。例如,H. sect.Deinanthe 和 sect.Cardiandra)的所有物种都具有草本和亚灌木生长习性。为区分下属类群提出了特征状态组合。基于稳健的系统发育框架,我们的研究结果表明绣球花形态特征具有复杂的进化历史。按照单系的标准,并考虑到单个和组合特征的形态一致性和同形性来诊断相关世系,我们更新了绣球花的分类,将其分为 5 个亚属和 19 个科。我们提出的分类方案基于稳健的系统发生学框架和深入的特征研究,为绣球花属下的细分提供了最新的视角。
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引用次数: 0
(3021–3022) Proposals to conserve the names Brochoneura, with a conserved type, and Cephalosphaera (Myristicaceae) (3021-3022) 关于保留 Brochoneura(有一个保留类型)和 Cephalosphaera(肉豆蔻科)名称的建议
IF 3.4 2区 生物学 Q2 EVOLUTIONARY BIOLOGY Pub Date : 2024-03-21 DOI: 10.1002/tax.13155
Zacky Ezedin, Hervé Sauquet
<p>(3021) <b><i>Brochoneura</i></b> Warb. in Engler, Pflanzenw. Ost-Afrikas C: 179. Jul 1895 [<i>Myristic</i>.], nom. cons. prop.</p><p>Typus: <i>B. madagascariensis</i> (Lam.) Warb. (in Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 68: 234. Dec 1897) (<i>Myristica madagascariensis</i> Lam.), typ. cons. prop.</p><p>(3022) <b><i>Cephalosphaera</i></b> Warb. in Bot. Jahrb. Syst. 33: 383. 13 Mar 1903 [<i>Myristic</i>.], nom. cons. prop.</p><p>Typus: <i>C. usambarensis</i> (Warb.) Warb. (<i>Brochoneura usambarensis</i> Warb.).</p><p><i>Myristicaceae</i> is a pantropical family of angiosperms comprising 21 genera and ca. 500 species. Recently, Figueiredo & Smith (in Phytotaxa 456: 299–300. 2020) proposed nomenclatural changes for the generic names <i>Brochoneura</i> and <i>Cephalosphaera</i>. Prior to their proposal, the name <i>Brochoneura</i> had been applied to a group of three species in Madagascar (Sauquet in Bot. J. Linn. Soc. 146: 351–368. 2004) whereas <i>Cephalosphaera</i> was exclusively applied to a single East African species. The proposed changes would have the name <i>Brochoneura</i> instead applied to the East African species while the Malagasy group would be renamed <i>Neobrochoneura</i> Figueiredo & Gideon F. Sm. This proposed name swap by Figueiredo & Smith followed their discovery of what may have been an unintentional name swap made by Otto Warburg, who originally published the name <i>Brochoneura</i> for the East African species (Warburg in Engler, Pflanzenw. Ost-Afrikas C: 180. 1895) and subsequently expanded the genus to incorporate three Malagasy species originally included in <i>Myristica</i> (Warburg in Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 68: 237. 1897). Later, he published the monotypic East African genus <i>Cephalosphaera</i> (Warburg in Bot. Jahrb. Syst. 33: 383. 1903) for <i>B. usambarensis</i>, the original type of <i>Brochoneura</i>, while restricting <i>Brochoneura</i> to the Malagasy group. To rectify this centuries-old error by Warburg, the authors proposed to have <i>Brochoneura</i> reinstated for the monotypic East African genus and give the Malagasy group a new name, <i>Neobrochoneura</i>.</p><p>Although the name switch only affects a handful of species, it is nonetheless not helpful and may result in confusion, especially since the names in their pre-2020 sense have become well-established in the taxonomic and floristic literature. The name <i>Brochoneura</i> has been applied to the Malagasy group for well over a century whereas it had only been applied to the East African taxon for a mere eight years, namely from 1895 to 1903. Both genera also have important economic uses.</p><p>The East African <i>Cephalosphaera</i> (vernacular: mtambao) has historically been regarded as an economically valuable timber species, having been selectively logged since at least the mid-20th century (Waser & al. in Tanzania J. Forest. Nat. Conserv. 82(2): 42–49. 2013). In the 1960s, it wa
(3021) Brochoneura Warb.Ost-Afrikas C: 179.Jul 1895 [Myristic.], nom:B. madagascariensis (Lam.) Warb. (in Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 68: 234. Dec 1897) (Myristica madagascariensis Lam.), typ. cons. prop.(3022) Cephalosphaera Warb. in Bot.Jahrb.Syst.33: 383.13 Mar 1903 [Myristic.], nom:C. usambarensis (Warb.) Warb. (Brochoneura usambarensis Warb.).Myristicaceae 是泛热带被子植物科,包括 21 属和大约 500 种。最近,Figueiredo &amp; Smith (in Phytotaxa 456: 299-300. 2020) 提议更改 Brochoneura 和 Cephalosphaera 这两个属名的命名。在他们提出建议之前,Brochoneura 这个名称一直用于马达加斯加的一组三个物种(Sauquet in Bot. J. Linn. Soc. 146: 351-368. 2004),而 Cephalosphaera 仅用于东非的一个物种。拟议的更改将使 Brochoneura 这一名称适用于东非种,而马达加斯加种群将更名为 Neobrochoneura Figueiredo &amp; Gideon F. Sm.Figueiredo &amp; Smith 提议的名称互换是在他们发现奥托-沃伯格(Otto Warburg)可能无意中进行了名称互换之后提出的,沃伯格最初将东非种命名为 Brochoneura(沃伯格在 Engler,Pflanzenw.Caes.Leop.-Carol.德国。Nat.Cur.68: 237.1897).后来,他为 Brochoneura 的原始模式 B. usambarensis 发表了单型的东非属 Cephalosphaera(沃伯格在 Bot. Jahrb. Syst.为了纠正沃伯格的这一千古错误,作者建议将 Brochoneura 恢复为单型的东非属,并给马达加斯加群一个新的名称--Neobrochoneura。虽然名称转换只影响了少数几个物种,但这并无益处,而且可能会造成混淆,尤其是 2020 年之前的名称已经在分类学和植物学文献中确立。马达加斯加类群使用 Brochoneura 这一名称已长达一个多世纪,而东非类群使用这一名称仅有八年时间,即从 1895 年到 1903 年。这两个属都有重要的经济用途。东非头尾杉(白话:mtambao)历来被视为具有经济价值的木材树种,至少从 20 世纪中期开始就被有选择性地砍伐(Waser &amp; al.Nat.Conserv.82(2):42-49.2013).20 世纪 60 年代,该树种被认为是 "最有用的多用途用材树种之一",20 世纪 70 年代,该树种成为胶合板的 "主要来源",最终导致其在 1985 年东乌桑巴拉山脉最重要木材清单中排名第八(Lemmens &amp; al.7: 199. 2012)。马达加斯加的 Brochoneura(白话:mafotra, rara)也同样被报道为一个具有重要经济价值的类群,其物种 B. acuminata Warb.具有从建筑到医药等多种用途(Bollen &amp; Donati in Oryx 40: 1-10.2006; Onjalalaina &amp; al. in Forests 12(566):1-20.2021).众所周知,B. acuminata 树种还具有重要的生态意义。它是马达加斯加东部低地热带森林中最丰富的树种之一,马达加斯加东南部记录的密度估计为 104 棵/公顷(Campera &amp; al. in Land (Basel) 12(81):1-20.2023).此外,B.acuminata是几种狐猴的重要食物来源,其中包括南方毛狐猴(Avahi meridionalis)和密特迈尔狐猴(Lepilemur mittermeieri),前者在枯萎季节将该树作为其第二大首选食物(Balestri,马达加斯加东南部Tsitongambarika保护区的南方毛狐猴(Avahi meridionalis)的生态学与保护 [Ph. D. dissertation, Oxford University Press.博士论文,牛津布鲁克斯大学,牛津]。2018; Wilmet &amp; al.2020 年)。Brochoneura 和 Cephalosphaera 这两个名称广泛出现在植物学文献和地区名录中(例如,Ngumbau &amp; al.)在科学文献中,即使在 Figueiredo &amp; Smith 发表文章之后,这些名称仍然沿用 2020 年之前的含义(例如,Ndangalasi &amp; al. in PLoS ONE 16(5): e0250859.2021; Raharisoa &amp; al. in J. Pharmacogn.Phytochem.10: 104-109.2021; Frost &amp; al. in J. Biogeogr:156-170.2022; Cheek &amp; Luke in Kew Bull.78: 469-497.2023; and Lolila &amp; al. in PLoS ONE 18(3): e0282528.2023).这表明,这些名称在多个领域的研究人员中已得到广泛认可。
{"title":"(3021–3022) Proposals to conserve the names Brochoneura, with a conserved type, and Cephalosphaera (Myristicaceae)","authors":"Zacky Ezedin, Hervé Sauquet","doi":"10.1002/tax.13155","DOIUrl":"https://doi.org/10.1002/tax.13155","url":null,"abstract":"&lt;p&gt;(3021) &lt;b&gt;&lt;i&gt;Brochoneura&lt;/i&gt;&lt;/b&gt; Warb. in Engler, Pflanzenw. Ost-Afrikas C: 179. Jul 1895 [&lt;i&gt;Myristic&lt;/i&gt;.], nom. cons. prop.&lt;/p&gt;\u0000&lt;p&gt;Typus: &lt;i&gt;B. madagascariensis&lt;/i&gt; (Lam.) Warb. (in Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 68: 234. Dec 1897) (&lt;i&gt;Myristica madagascariensis&lt;/i&gt; Lam.), typ. cons. prop.&lt;/p&gt;\u0000&lt;p&gt;(3022) &lt;b&gt;&lt;i&gt;Cephalosphaera&lt;/i&gt;&lt;/b&gt; Warb. in Bot. Jahrb. Syst. 33: 383. 13 Mar 1903 [&lt;i&gt;Myristic&lt;/i&gt;.], nom. cons. prop.&lt;/p&gt;\u0000&lt;p&gt;Typus: &lt;i&gt;C. usambarensis&lt;/i&gt; (Warb.) Warb. (&lt;i&gt;Brochoneura usambarensis&lt;/i&gt; Warb.).&lt;/p&gt;\u0000&lt;p&gt;&lt;i&gt;Myristicaceae&lt;/i&gt; is a pantropical family of angiosperms comprising 21 genera and ca. 500 species. Recently, Figueiredo &amp; Smith (in Phytotaxa 456: 299–300. 2020) proposed nomenclatural changes for the generic names &lt;i&gt;Brochoneura&lt;/i&gt; and &lt;i&gt;Cephalosphaera&lt;/i&gt;. Prior to their proposal, the name &lt;i&gt;Brochoneura&lt;/i&gt; had been applied to a group of three species in Madagascar (Sauquet in Bot. J. Linn. Soc. 146: 351–368. 2004) whereas &lt;i&gt;Cephalosphaera&lt;/i&gt; was exclusively applied to a single East African species. The proposed changes would have the name &lt;i&gt;Brochoneura&lt;/i&gt; instead applied to the East African species while the Malagasy group would be renamed &lt;i&gt;Neobrochoneura&lt;/i&gt; Figueiredo &amp; Gideon F. Sm. This proposed name swap by Figueiredo &amp; Smith followed their discovery of what may have been an unintentional name swap made by Otto Warburg, who originally published the name &lt;i&gt;Brochoneura&lt;/i&gt; for the East African species (Warburg in Engler, Pflanzenw. Ost-Afrikas C: 180. 1895) and subsequently expanded the genus to incorporate three Malagasy species originally included in &lt;i&gt;Myristica&lt;/i&gt; (Warburg in Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 68: 237. 1897). Later, he published the monotypic East African genus &lt;i&gt;Cephalosphaera&lt;/i&gt; (Warburg in Bot. Jahrb. Syst. 33: 383. 1903) for &lt;i&gt;B. usambarensis&lt;/i&gt;, the original type of &lt;i&gt;Brochoneura&lt;/i&gt;, while restricting &lt;i&gt;Brochoneura&lt;/i&gt; to the Malagasy group. To rectify this centuries-old error by Warburg, the authors proposed to have &lt;i&gt;Brochoneura&lt;/i&gt; reinstated for the monotypic East African genus and give the Malagasy group a new name, &lt;i&gt;Neobrochoneura&lt;/i&gt;.&lt;/p&gt;\u0000&lt;p&gt;Although the name switch only affects a handful of species, it is nonetheless not helpful and may result in confusion, especially since the names in their pre-2020 sense have become well-established in the taxonomic and floristic literature. The name &lt;i&gt;Brochoneura&lt;/i&gt; has been applied to the Malagasy group for well over a century whereas it had only been applied to the East African taxon for a mere eight years, namely from 1895 to 1903. Both genera also have important economic uses.&lt;/p&gt;\u0000&lt;p&gt;The East African &lt;i&gt;Cephalosphaera&lt;/i&gt; (vernacular: mtambao) has historically been regarded as an economically valuable timber species, having been selectively logged since at least the mid-20th century (Waser &amp; al. in Tanzania J. Forest. Nat. Conserv. 82(2): 42–49. 2013). In the 1960s, it wa","PeriodicalId":49448,"journal":{"name":"Taxon","volume":"31 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2024-03-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140202017","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Epitypification of the Linnaean Statice echioides (Plumbaginaceae) and notes on Smith's concepts of S. aristata and S. rorida Linnaean Statice echioides(Plumbaginaceae)的外显和 Smith 对 S. aristata 和 S. rorida 概念的注释
IF 3.4 2区 生物学 Q2 EVOLUTIONARY BIOLOGY Pub Date : 2024-03-19 DOI: 10.1002/tax.13165
Duilio Iamonico
The typification of the Linnaean name Statice echioides (currently Limonium echioides) is discussed. An illustration from Magnol's Botanicum Monspeliense (“Limonium minus annuum bullatis foliis vel echioides”) was correctly designated as lectotype by Erben in 1978 according to Art. 7.11 of Shenzhen Code. However, this image lacks some of the important flower characters required for a critical identification of the species. An epitype (plate no. 299 in Sibthorp & Smith's Flora Graeca) is selected to serve as an interpretative type of the lectotype of S. echioides (Art. 9.6). In addition, the name S. aristata, published in Sibthorp & Smith's Flora Graecae prodromus, is discussed in depth and lectotypified on the above‐mentioned Magnol illustration, making this name homotypic with the Linnaean one. Finally, the concept of S. echioides, as described in Flora Graecae prodromus, is discussed, concluding that it refers to the currently recognized Limonium roridum (≡ S. rorida, as originally published in Flora Graeca).
讨论了林奈学名 Statice echioides(现名 Limonium echioides)的类型化问题。1978 年,埃尔本根据《深圳植物志》第 7.11 条的规定,将马格诺尔(Magnol)的《蒙斯佩利昂植物志》中的一幅插图("Limonium minus annuum bullatis foliis vel echioides")正确地指定为标准模式。深圳规范》第 7.11 条。然而,这幅图缺乏对该种进行重要鉴定所需的一些重要花特征。echioides 的标准模式(第 9.6 条)。此外,对发表在 Sibthorp & Smith 的《Flora Graecae prodromus》中的 S. aristata 这一名称进行了深入讨论,并根据上述 Magnol 插图对其进行了讲座模式化,从而使该名称与林奈名称同型。最后,讨论了《Flora Graecae prodromus》中描述的 S. echioides 的概念,认为它指的是目前公认的 Limonium roridum(≡ S. rorida,最初发表于《Flora Graeca》)。
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引用次数: 0
(3016) Proposal to reject the name Opuntia aulacothele (Cactaceae) (3016) 关于否决 Opuntia aulacothele(仙人掌科)名称的建议
IF 3.4 2区 生物学 Q2 EVOLUTIONARY BIOLOGY Pub Date : 2024-03-11 DOI: 10.1002/tax.13161
Urs Eggli, Felix F. Merklinger
{"title":"(3016) Proposal to reject the name Opuntia aulacothele (Cactaceae)","authors":"Urs Eggli, Felix F. Merklinger","doi":"10.1002/tax.13161","DOIUrl":"https://doi.org/10.1002/tax.13161","url":null,"abstract":"","PeriodicalId":49448,"journal":{"name":"Taxon","volume":"8 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2024-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140128180","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
(3017) Proposal to conserve the name Gymnosporia royleana (Celastraceae) (3017) 关于保留 Gymnosporia royleana(天南星科)名称的建议
IF 3.4 2区 生物学 Q2 EVOLUTIONARY BIOLOGY Pub Date : 2024-03-07 DOI: 10.1002/tax.13159
Abhishek T. Bhat, K.M. Prabhukumar, Tikam Singh Rana
<p>(3017) <b><i>Gymnosporia royleana</i></b> M.A. Lawson in Hooker, Fl. Brit. India 1: 620. Feb 1875 [Angiosp.: <i>Celastr</i>.], nom. cons. prop.</p><p><b>Lectotypus (hic designatus):</b> “Affghania” [Afghanistan], <i>Griffith 1245</i> (K barcode K001325915 [digital image!]; isolectotypus: K001325917 [digital image!]).</p><p>Wallich (Numer. List: 151, no. 4317. 1831) listed “<i>C</i>[<i>elastrus</i>]. <i>Royleana</i> Wall.”, based on a Royle collection. Subsequently, Royle (Ill. Bot. Himal. Mts.: 167. 1835) recorded “<i>C. spinosus</i> nob. <i>Ic. ined</i>. t. 73”. Both, being nomina nuda, are not validly published names. However, <i>Celastrus spinosus</i> was later validated by Boissier (Fl. Orient. 2: 11. 1872).</p><p>Lawson (in Hooker, Fl. Brit. India 1: 620. 1875), while revising the family <i>Celastraceae</i>, transferred a few members of <i>Celastrus</i> to <i>Gymnosporia</i>. He thus inadvertently validly published <i>Gymnosporia royleana</i> seemingly based on the invalid “<i>C. royleanus</i> Wall.” Lawson (l.c.) also included <i>C. spinosus</i> Royle ex Boiss. as a synonym. His choice in accepting <i>G. royleana</i> was seemingly purely based on what he considered to be priority of publication. This nomenclatural error under current rules made <i>G. royleana</i> a superfluous illegitimate name under Art. 52.1 of the <i>ICN</i> (Turland & al. in Regnum Veg. 2018) as Lawson (l.c.) should have adopted the then-available epithet “<i>spinosa</i>”. It is thus automatically typified by the type of <i>C. spinosus</i> Boiss. (Art. 7.5). Boissier (l.c.) cited two gatherings from Afghanistan (“Griffith pl. exs. 1245! et Herb. East lnd. Comp. n<sup>o</sup> 1991!”). During our search for type specimens, we traced eight specimens, six at K [barcodes K001325915, K001325916, K001325917, K001325918, K001325919, K001325920] and one each at CAL [No. 86591] and DD [No. 1991]. The sheet K001325915 is well preserved, precisely matching with the protologue, bearing one flowering and a fruiting twig of a single gathering [1245] without any confusing and illegible labels. Hence, it is selected above as the lectotype; the specimen K001325917 appears to be a duplicate of it.</p><p>Cufodontis (in Senckenberg. Biol. 43: 313. 1962) transferred <i>Gymnosporia royleana</i> to <i>Maytenus</i> as <i>M. royleana</i> Cufod., which is a legitimate name, as the existence of <i>M. spinosa</i> (Griseb.) Lourteig & O'Donell (in Natura (Buenos Aires) 1: 188. 1955) precluded the adoption of Boissier's epithet ‘<i>spinosa</i>’ in <i>Maytenus</i>. Raju & Babu (in Bull. Bot. Surv. India 10: 348. 1969) opined that Kanjilal (Forest Fl. School Circle: 68. 1901) had validated <i>Celastrus royleanus</i>. However, <i>C. royleanus</i> Wall. ex Kanjilal is also an illegitimate name as <i>C. spinosus</i> was included in its synonymy.</p><p>The species known as <i>Gymnosporia royleana</i> is distributed in Afghanistan, India, Pakistan, Tibet, and West Himalaya (POWO, 2023 ht
然而,最近的形态学和分子系统发育研究支持区分这两个属,因此 Gymnosporia 被恢复为一个独立的属(Jordaan &amp; van Wyk in S. African J. Bot.65: 177.1999; Simmons &amp; al.J. Bot.88: 321.2001; Simmons &amp; al. in Molec.Phylogen.19: 363.2001).此外,Gymnosporia 仅分布于包括印度在内的旧大陆国家(Jordaan &amp; van Wyk, l.c. 1999),Maytenus 的所有旧大陆刺种都被转入 Gymnosporia(Jordaan &amp; van Wyk, l.c. 2006: 515)。目前,Maytenus yimenensis H. Shao (in Bull. Bot. Res、2000)被视为 Gymnosporia royleana(POWO,2023 https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:1020820-1)的异名。因此,可以采用 "yimenensis "这一特异性名称来命名 G. yimenensis。然而,鉴于上述原因,将特异性表名 "yimenensis "引入已确立的 G. royleana 会破坏命名的稳定性,造成严重混淆。因此,我们建议按照第 14.1 和 14.2 条的规定,保留不合法的 Gymnosporia royleana M.A. Lawson。14.1 &amp; 14.2。
{"title":"(3017) Proposal to conserve the name Gymnosporia royleana (Celastraceae)","authors":"Abhishek T. Bhat, K.M. Prabhukumar, Tikam Singh Rana","doi":"10.1002/tax.13159","DOIUrl":"https://doi.org/10.1002/tax.13159","url":null,"abstract":"&lt;p&gt;(3017) &lt;b&gt;&lt;i&gt;Gymnosporia royleana&lt;/i&gt;&lt;/b&gt; M.A. Lawson in Hooker, Fl. Brit. India 1: 620. Feb 1875 [Angiosp.: &lt;i&gt;Celastr&lt;/i&gt;.], nom. cons. prop.&lt;/p&gt;\u0000&lt;p&gt;&lt;b&gt;Lectotypus (hic designatus):&lt;/b&gt; “Affghania” [Afghanistan], &lt;i&gt;Griffith 1245&lt;/i&gt; (K barcode K001325915 [digital image!]; isolectotypus: K001325917 [digital image!]).&lt;/p&gt;\u0000&lt;p&gt;Wallich (Numer. List: 151, no. 4317. 1831) listed “&lt;i&gt;C&lt;/i&gt;[&lt;i&gt;elastrus&lt;/i&gt;]. &lt;i&gt;Royleana&lt;/i&gt; Wall.”, based on a Royle collection. Subsequently, Royle (Ill. Bot. Himal. Mts.: 167. 1835) recorded “&lt;i&gt;C. spinosus&lt;/i&gt; nob. &lt;i&gt;Ic. ined&lt;/i&gt;. t. 73”. Both, being nomina nuda, are not validly published names. However, &lt;i&gt;Celastrus spinosus&lt;/i&gt; was later validated by Boissier (Fl. Orient. 2: 11. 1872).&lt;/p&gt;\u0000&lt;p&gt;Lawson (in Hooker, Fl. Brit. India 1: 620. 1875), while revising the family &lt;i&gt;Celastraceae&lt;/i&gt;, transferred a few members of &lt;i&gt;Celastrus&lt;/i&gt; to &lt;i&gt;Gymnosporia&lt;/i&gt;. He thus inadvertently validly published &lt;i&gt;Gymnosporia royleana&lt;/i&gt; seemingly based on the invalid “&lt;i&gt;C. royleanus&lt;/i&gt; Wall.” Lawson (l.c.) also included &lt;i&gt;C. spinosus&lt;/i&gt; Royle ex Boiss. as a synonym. His choice in accepting &lt;i&gt;G. royleana&lt;/i&gt; was seemingly purely based on what he considered to be priority of publication. This nomenclatural error under current rules made &lt;i&gt;G. royleana&lt;/i&gt; a superfluous illegitimate name under Art. 52.1 of the &lt;i&gt;ICN&lt;/i&gt; (Turland &amp; al. in Regnum Veg. 2018) as Lawson (l.c.) should have adopted the then-available epithet “&lt;i&gt;spinosa&lt;/i&gt;”. It is thus automatically typified by the type of &lt;i&gt;C. spinosus&lt;/i&gt; Boiss. (Art. 7.5). Boissier (l.c.) cited two gatherings from Afghanistan (“Griffith pl. exs. 1245! et Herb. East lnd. Comp. n&lt;sup&gt;o&lt;/sup&gt; 1991!”). During our search for type specimens, we traced eight specimens, six at K [barcodes K001325915, K001325916, K001325917, K001325918, K001325919, K001325920] and one each at CAL [No. 86591] and DD [No. 1991]. The sheet K001325915 is well preserved, precisely matching with the protologue, bearing one flowering and a fruiting twig of a single gathering [1245] without any confusing and illegible labels. Hence, it is selected above as the lectotype; the specimen K001325917 appears to be a duplicate of it.&lt;/p&gt;\u0000&lt;p&gt;Cufodontis (in Senckenberg. Biol. 43: 313. 1962) transferred &lt;i&gt;Gymnosporia royleana&lt;/i&gt; to &lt;i&gt;Maytenus&lt;/i&gt; as &lt;i&gt;M. royleana&lt;/i&gt; Cufod., which is a legitimate name, as the existence of &lt;i&gt;M. spinosa&lt;/i&gt; (Griseb.) Lourteig &amp; O'Donell (in Natura (Buenos Aires) 1: 188. 1955) precluded the adoption of Boissier's epithet ‘&lt;i&gt;spinosa&lt;/i&gt;’ in &lt;i&gt;Maytenus&lt;/i&gt;. Raju &amp; Babu (in Bull. Bot. Surv. India 10: 348. 1969) opined that Kanjilal (Forest Fl. School Circle: 68. 1901) had validated &lt;i&gt;Celastrus royleanus&lt;/i&gt;. However, &lt;i&gt;C. royleanus&lt;/i&gt; Wall. ex Kanjilal is also an illegitimate name as &lt;i&gt;C. spinosus&lt;/i&gt; was included in its synonymy.&lt;/p&gt;\u0000&lt;p&gt;The species known as &lt;i&gt;Gymnosporia royleana&lt;/i&gt; is distributed in Afghanistan, India, Pakistan, Tibet, and West Himalaya (POWO, 2023 ht","PeriodicalId":49448,"journal":{"name":"Taxon","volume":"26 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2024-03-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140076400","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
(3014) Proposal to conserve the name Clitocybe (Basidiomycota) with a conserved type (3014) 关于保留 Clitocybe(担子菌纲)名称和保留类型的建议
IF 3.4 2区 生物学 Q2 EVOLUTIONARY BIOLOGY Pub Date : 2024-03-07 DOI: 10.1002/tax.13149
Zheng-Mi He, Zhu L. Yang
<p>(3014) <b><i>Clitocybe</i></b> (Fr.) Staude, Schwämme Mitteldeutschl.: xxviii, 122. 1857 ≡ <b><i>Agaricus</i></b> “trib.” <b><i>Clitocybe</i></b> Fr., Syst. Mycol. 1: 9, 78. 1 Jan 1821, nom. sanct. (Fries, ibid.), nom. cons. prop.</p><p>Typus: <i>Agaricus phyllophilus</i> Pers., nom. sanct. (<i>C</i>. <i>phyllophila</i> (Pers.) P. Kumm.), typ. cons. prop.</p><p><i>Clitocybe</i> (Fr.) Staude (Schwämme Mitteldeutschl.: xxviii, 122. 1857) is a genus of the family <i>Clitocybaceae</i> Vizzini & al. (in Index Fungorum 462: 1. 2020), characterized by the clitocyboid basidiome typically with a depressed pileus and decurrent lamellae. The genus currently encompasses approximately 500 species, according to the Index Fungorum database (www.indexfungorum.org, accessed on 1 Oct 2023). A substantial proportion of these species is included in specific monographs of Harmaja (in Karstenia 10: 5–168. 1969) and Bigelow (N. Amer. Sp. Clitocybe 1. 1982; 2. 1985). The genus exhibits a wide global distribution, and has also been extensively documented in various comprehensive monographs, journals or field guides from Africa (e.g., Pegler in Persoonia 4: 73–124. 1966), Asia (e.g., Li & al., Atlas Chinese Macrofungal Resources. 2015), Europe (e.g., Bas & al., Fl. Agaricina Neerl. 3. 1995), North America (e.g., Phillips, Mushrooms Other Fungi N. Amer. 2005), South America (e.g., Dennis, Fungus Fl. Venezuela. 1970), Australia (Grgurinovic, Larger Fungi S. Australia. 1997), and New Zealand (e.g., Cooper, New Zealand Clitocybaceae. 2016). The genus has been demonstrated to serve as a valuable reservoir of edible and medicinal resources (Wu & al. in Fungal Diversity 98: 1–76. 2019). Meanwhile, the genus has also been found to contain numerous muscarine-producing poisonous mushrooms (Genest & al. in J. Pharmacol. Sci. 57: 331–333. 1968; He & al. in Fungal Diversity 123: 1–47. 2023).</p><p>Recent multi-locus phylogenetic and phylogenomic analyses of <i>Clitocybaceae</i>, conducted by He & al. (l.c.), revealed the presence of six generic clades based on comprehensive assessments of genetic distance and divergence time. In the phylograms, the genera <i>Dendrocollybia</i>, <i>Lepista</i> s.str., <i>Pseudolyophyllum</i>, and <i>Singerocybe</i> each formed a distinct clade, whereas <i>Clitocybe</i> fell into the remaining two generic clades. The first clade exhibited robustness, encompassing the majority of traditional <i>Clitocybe</i>, <i>Collybia</i>, and <i>Lepista</i> species, while the second clade comprised only a few <i>Clitocybe</i> species.</p><p>The first generic clade can be divided into four subclades, including species previously classified under (1) <i>Clitocybe</i> sect. <i>Candicantes</i> (Quél.) Konrad & Maubl. (Icon. Select. Fung. 10: 331. 1937), <i>C</i>. sect. <i>Odorae</i> H.E. Bigelow (l.c. 1982: 148), and <i>Collybia</i> s.str. (Fr.) Staude (l.c.), (2) <i>Lepista</i> sect. <i>Nuda</i> Harmaja (in Karstenia 18: 49–54. 197
edu/botany/codes-proposals/),但 Gymnopus 的模式种(G. purus (Pers.) Gray)目前被视为 Myceaceae 中的 Mycena pura (Pers.) P. Kumm.,与 Clitocybaceae 属于不同的姬松茸亚目。因此,Gymnopus 并不威胁 Clitocybe,后者也无需与之相对应。必要的修订包括:(1)将前述 Collybia s.str.的其余 3 个种,以及最近由 He &amp; al.因此,与几百个新组合(包括与 Infundibulicybe 只有很远的亲缘关系的约 30 个种)相比,如果按照建议不改变 Clitocybe 的模式而保留新的模式,则需要将其归入 Clitocybe。
{"title":"(3014) Proposal to conserve the name Clitocybe (Basidiomycota) with a conserved type","authors":"Zheng-Mi He, Zhu L. Yang","doi":"10.1002/tax.13149","DOIUrl":"https://doi.org/10.1002/tax.13149","url":null,"abstract":"&lt;p&gt;(3014) &lt;b&gt;&lt;i&gt;Clitocybe&lt;/i&gt;&lt;/b&gt; (Fr.) Staude, Schwämme Mitteldeutschl.: xxviii, 122. 1857 ≡ &lt;b&gt;&lt;i&gt;Agaricus&lt;/i&gt;&lt;/b&gt; “trib.” &lt;b&gt;&lt;i&gt;Clitocybe&lt;/i&gt;&lt;/b&gt; Fr., Syst. Mycol. 1: 9, 78. 1 Jan 1821, nom. sanct. (Fries, ibid.), nom. cons. prop.&lt;/p&gt;\u0000&lt;p&gt;Typus: &lt;i&gt;Agaricus phyllophilus&lt;/i&gt; Pers., nom. sanct. (&lt;i&gt;C&lt;/i&gt;. &lt;i&gt;phyllophila&lt;/i&gt; (Pers.) P. Kumm.), typ. cons. prop.&lt;/p&gt;\u0000&lt;p&gt;&lt;i&gt;Clitocybe&lt;/i&gt; (Fr.) Staude (Schwämme Mitteldeutschl.: xxviii, 122. 1857) is a genus of the family &lt;i&gt;Clitocybaceae&lt;/i&gt; Vizzini &amp; al. (in Index Fungorum 462: 1. 2020), characterized by the clitocyboid basidiome typically with a depressed pileus and decurrent lamellae. The genus currently encompasses approximately 500 species, according to the Index Fungorum database (www.indexfungorum.org, accessed on 1 Oct 2023). A substantial proportion of these species is included in specific monographs of Harmaja (in Karstenia 10: 5–168. 1969) and Bigelow (N. Amer. Sp. Clitocybe 1. 1982; 2. 1985). The genus exhibits a wide global distribution, and has also been extensively documented in various comprehensive monographs, journals or field guides from Africa (e.g., Pegler in Persoonia 4: 73–124. 1966), Asia (e.g., Li &amp; al., Atlas Chinese Macrofungal Resources. 2015), Europe (e.g., Bas &amp; al., Fl. Agaricina Neerl. 3. 1995), North America (e.g., Phillips, Mushrooms Other Fungi N. Amer. 2005), South America (e.g., Dennis, Fungus Fl. Venezuela. 1970), Australia (Grgurinovic, Larger Fungi S. Australia. 1997), and New Zealand (e.g., Cooper, New Zealand Clitocybaceae. 2016). The genus has been demonstrated to serve as a valuable reservoir of edible and medicinal resources (Wu &amp; al. in Fungal Diversity 98: 1–76. 2019). Meanwhile, the genus has also been found to contain numerous muscarine-producing poisonous mushrooms (Genest &amp; al. in J. Pharmacol. Sci. 57: 331–333. 1968; He &amp; al. in Fungal Diversity 123: 1–47. 2023).&lt;/p&gt;\u0000&lt;p&gt;Recent multi-locus phylogenetic and phylogenomic analyses of &lt;i&gt;Clitocybaceae&lt;/i&gt;, conducted by He &amp; al. (l.c.), revealed the presence of six generic clades based on comprehensive assessments of genetic distance and divergence time. In the phylograms, the genera &lt;i&gt;Dendrocollybia&lt;/i&gt;, &lt;i&gt;Lepista&lt;/i&gt; s.str., &lt;i&gt;Pseudolyophyllum&lt;/i&gt;, and &lt;i&gt;Singerocybe&lt;/i&gt; each formed a distinct clade, whereas &lt;i&gt;Clitocybe&lt;/i&gt; fell into the remaining two generic clades. The first clade exhibited robustness, encompassing the majority of traditional &lt;i&gt;Clitocybe&lt;/i&gt;, &lt;i&gt;Collybia&lt;/i&gt;, and &lt;i&gt;Lepista&lt;/i&gt; species, while the second clade comprised only a few &lt;i&gt;Clitocybe&lt;/i&gt; species.&lt;/p&gt;\u0000&lt;p&gt;The first generic clade can be divided into four subclades, including species previously classified under (1) &lt;i&gt;Clitocybe&lt;/i&gt; sect. &lt;i&gt;Candicantes&lt;/i&gt; (Quél.) Konrad &amp; Maubl. (Icon. Select. Fung. 10: 331. 1937), &lt;i&gt;C&lt;/i&gt;. sect. &lt;i&gt;Odorae&lt;/i&gt; H.E. Bigelow (l.c. 1982: 148), and &lt;i&gt;Collybia&lt;/i&gt; s.str. (Fr.) Staude (l.c.), (2) &lt;i&gt;Lepista&lt;/i&gt; sect. &lt;i&gt;Nuda&lt;/i&gt; Harmaja (in Karstenia 18: 49–54. 197","PeriodicalId":49448,"journal":{"name":"Taxon","volume":"32 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2024-03-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140073263","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
(3018) Proposal to reject the name Cheiranthus armeniacus (Erysimum armeniacum) (Cruciferae) (3018)关于否决 "Cheiranthus armeniacus"(Erysimum armeniacum)(十字花科)名称的建议
IF 3.4 2区 生物学 Q2 EVOLUTIONARY BIOLOGY Pub Date : 2024-03-07 DOI: 10.1002/tax.13160
Dmitry A. German
<p>(3018) <b><i>Cheiranthus armeniacus</i></b> Sims in Bot. Mag.: t. 835. 1 Mai 1805 [Angiosp.: <i>Cruc</i>.], nom. rej. prop.</p><p><b>Lectotypus (hic designatus):</b> [icon in] Bot. Mag.: t. 835. 1 Mai 1805.</p><p>The name <i>Cheiranthus armeniacus</i> Sims (in Bot. Mag.: t. 835. 1805), the basionym of <i>Erysimum armeniacum</i> (Sims) J. Gay (Erysim. Nov.: 8. 1842), is the earliest available for the group of 3–4 predominantly Caucasian, basically biennial species of <i>Erysimum</i> L. referred to as <i>E</i>. subsect. <i>Iberica</i> V.I. Dorof. (in Bot. Zhurn. (Moscow & Leningrad) 72: 1538. 1987). In spite of this, its use has been most discontinuous for over two centuries and its interpretation remains unstable and still seriously varying among authors.</p><p>Description of <i>Cheiranthus armeniacus</i> was based on cultivated plants grown from seeds collected on Mount Ararat in eastern Anatolia. No relevant herbarium material seems to be extant, as suggested by Davis & al. (Fl. Turkey 10: 55. 1988; the author's search in K and elsewhere also failed), and trichome morphology, critically important in the taxonomy of <i>Erysimum</i>, was not described in the protologue. However, the original illustration, designated above as lectotype, showing the characteristic habit along with some mentioned details (e.g., stout sulcate stem, big and profoundly bilobed stigmas, erect young fruits) allows for defining its affinity. Bieberstein (Fl. Taur.-Caucas. 2: 118. 1808) was the first to consider <i>C. armeniacus</i> conspecific with <i>C. ibericus</i> Adams (in Beitr. Naturk. 1: 61. 15 Nov 1805; see TL-2 No. 16,898), described from north-eastern Georgia (lectotypified by Polatschek in Ann. Naturhist. Mus. Wien, B, 111: 254. 2010: Georgia, Mtskheta-Mtianeti, Mt. Kaishauri, <i>A.A. Musin-Pushkin</i> [B-W No. 12086-03]), and was followed by Candolle, who adopted the name <i>E. ibericum</i> (Adams) DC. (Syst. Nat. 2: 498. 1821) for the species. This synonymy was included in early synoptic accounts (Sprengel, Syst. Veg. 2: 907. 1825; Steudel, Nomencl. Bot., ed. 2, 1: 346. 1840; Jackson in Index Kew. 1: 508, 892. 1893) and in a few floras (Ledebour, Fl. Ross. 1: 187. 1841 [“1842”]; Boissier, Fl. Orient. 1: 192. 1867; Busch in Kuznetsov & al., Fl. Cauc. Crit. 3(4): 526. 1909, in Komarov, Fl. SSSR 8: 101. 1939), in the latter two cases with respect to the illustration only. Recently this approach was revived by Zernov & al. (Opred. Sosud. Rast. Karachay-Cherkess. Resp.: [205]. 2015).</p><p>As an accepted species, <i>Cheiranthus armeniacus</i> was treated by Gay (l.c.), who transferred it to <i>Erysimum</i>, then, indirectly, by Ruprecht by exclusion of the name from synonymy of <i>Erysimastrum ibericum</i> (Adams) Rupr. (in Mém. Acad. Imp. Sci. Saint Pétersbourg, Sér. 7, 15(2) [Fl. Caucasi]: 75, 77. 1869) and the next time, after over 110 years, by Polatschek (in Willdenowia 13: 88. 1983), who mentioned that the species also occurs in the Cau
2008:163),一个非常密切相关的种被他视为亚美尼亚特有种(Polatschek, l.c. 2011: 469)。Avetisyan(l.c. 2009: 21)不同,他将 E. gabrielianiae 与 E. ibericum 同名,但后者也分布在全国各地(12 个花卉区中的 6 个)。因此,从地理学的角度来看,如果将 E. gabrielianiae 和 E. ibericum 分开处理,假设在阿拉拉特山上发现了这两种植物,或者换句话说,将其中任何一种描述为 Cheiranthus armeniacus 的可能性都差不多。然而,E. gabrielianiae 的形态特征,如卵状披针形、近全缘或有细锯齿的茎生叶,并不符合 C. armeniacus 的原型和 E. ibericum s.str. 的典型特征。此外,从 E.gabrielianiae在ERE、M、W 和其他标本馆(包括其模式标本采集地)的研究材料来看,本种(如果不是 Polatschek, l.c. 2011 年发现的通常为四倍体的 E. ibericum 的种下二倍体种族)是 E. subsect.亚种的唯一成员。伊比利亚严格来说是二年生植物,从未显示出形成木质块根的任何趋势。gabrielianiae 而 "拯救 E. ibericum "的理论尝试没有坚实的基础,而后者在分类学上的可疑地位进一步强调了这一问题。综上所述,鉴于在阿拉拉特山上出现与 Erysimum ibericum 习性相同的该组另一物种的可能性很低,拒绝使用 Cheiranthus armeniacus 这一名称似乎是最好的选择。另外,也可以考虑在多罗费耶夫(Dorofeyev,l.c. 1987 年及以后)的意义上,通过保存类型(或新的表型)来使用该名称,但由于在此意义上使用该名称的历史相对较短,而且目前已有三个名称,都经过了很好的表型和特征描述(其中两个具有同等的优先权,有可能在广泛意义上应用于相关物种),这种行为可能不受欢迎。因此,为了防止在广泛、明确和持续使用了 200 多年后,因直接应用《规范》而不可避免地将 E. ibericum 这一名称改为较早但长期被忽视、不连续和混乱地应用的 E. armeniacum 这一名称所造成的命名上的不稳定,在此建议摈弃 C. armeniacus 这一名称。
{"title":"(3018) Proposal to reject the name Cheiranthus armeniacus (Erysimum armeniacum) (Cruciferae)","authors":"Dmitry A. German","doi":"10.1002/tax.13160","DOIUrl":"https://doi.org/10.1002/tax.13160","url":null,"abstract":"&lt;p&gt;(3018) &lt;b&gt;&lt;i&gt;Cheiranthus armeniacus&lt;/i&gt;&lt;/b&gt; Sims in Bot. Mag.: t. 835. 1 Mai 1805 [Angiosp.: &lt;i&gt;Cruc&lt;/i&gt;.], nom. rej. prop.&lt;/p&gt;\u0000&lt;p&gt;&lt;b&gt;Lectotypus (hic designatus):&lt;/b&gt; [icon in] Bot. Mag.: t. 835. 1 Mai 1805.&lt;/p&gt;\u0000&lt;p&gt;The name &lt;i&gt;Cheiranthus armeniacus&lt;/i&gt; Sims (in Bot. Mag.: t. 835. 1805), the basionym of &lt;i&gt;Erysimum armeniacum&lt;/i&gt; (Sims) J. Gay (Erysim. Nov.: 8. 1842), is the earliest available for the group of 3–4 predominantly Caucasian, basically biennial species of &lt;i&gt;Erysimum&lt;/i&gt; L. referred to as &lt;i&gt;E&lt;/i&gt;. subsect. &lt;i&gt;Iberica&lt;/i&gt; V.I. Dorof. (in Bot. Zhurn. (Moscow &amp; Leningrad) 72: 1538. 1987). In spite of this, its use has been most discontinuous for over two centuries and its interpretation remains unstable and still seriously varying among authors.&lt;/p&gt;\u0000&lt;p&gt;Description of &lt;i&gt;Cheiranthus armeniacus&lt;/i&gt; was based on cultivated plants grown from seeds collected on Mount Ararat in eastern Anatolia. No relevant herbarium material seems to be extant, as suggested by Davis &amp; al. (Fl. Turkey 10: 55. 1988; the author's search in K and elsewhere also failed), and trichome morphology, critically important in the taxonomy of &lt;i&gt;Erysimum&lt;/i&gt;, was not described in the protologue. However, the original illustration, designated above as lectotype, showing the characteristic habit along with some mentioned details (e.g., stout sulcate stem, big and profoundly bilobed stigmas, erect young fruits) allows for defining its affinity. Bieberstein (Fl. Taur.-Caucas. 2: 118. 1808) was the first to consider &lt;i&gt;C. armeniacus&lt;/i&gt; conspecific with &lt;i&gt;C. ibericus&lt;/i&gt; Adams (in Beitr. Naturk. 1: 61. 15 Nov 1805; see TL-2 No. 16,898), described from north-eastern Georgia (lectotypified by Polatschek in Ann. Naturhist. Mus. Wien, B, 111: 254. 2010: Georgia, Mtskheta-Mtianeti, Mt. Kaishauri, &lt;i&gt;A.A. Musin-Pushkin&lt;/i&gt; [B-W No. 12086-03]), and was followed by Candolle, who adopted the name &lt;i&gt;E. ibericum&lt;/i&gt; (Adams) DC. (Syst. Nat. 2: 498. 1821) for the species. This synonymy was included in early synoptic accounts (Sprengel, Syst. Veg. 2: 907. 1825; Steudel, Nomencl. Bot., ed. 2, 1: 346. 1840; Jackson in Index Kew. 1: 508, 892. 1893) and in a few floras (Ledebour, Fl. Ross. 1: 187. 1841 [“1842”]; Boissier, Fl. Orient. 1: 192. 1867; Busch in Kuznetsov &amp; al., Fl. Cauc. Crit. 3(4): 526. 1909, in Komarov, Fl. SSSR 8: 101. 1939), in the latter two cases with respect to the illustration only. Recently this approach was revived by Zernov &amp; al. (Opred. Sosud. Rast. Karachay-Cherkess. Resp.: [205]. 2015).&lt;/p&gt;\u0000&lt;p&gt;As an accepted species, &lt;i&gt;Cheiranthus armeniacus&lt;/i&gt; was treated by Gay (l.c.), who transferred it to &lt;i&gt;Erysimum&lt;/i&gt;, then, indirectly, by Ruprecht by exclusion of the name from synonymy of &lt;i&gt;Erysimastrum ibericum&lt;/i&gt; (Adams) Rupr. (in Mém. Acad. Imp. Sci. Saint Pétersbourg, Sér. 7, 15(2) [Fl. Caucasi]: 75, 77. 1869) and the next time, after over 110 years, by Polatschek (in Willdenowia 13: 88. 1983), who mentioned that the species also occurs in the Cau","PeriodicalId":49448,"journal":{"name":"Taxon","volume":"106 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2024-03-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140073300","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
DNA barcoding of the genus Verbascum (Scrophulariaceae) in the Arabian Peninsula 阿拉伯半岛马鞭草属(景天科)的 DNA 条形编码
IF 3.4 2区 生物学 Q2 EVOLUTIONARY BIOLOGY Pub Date : 2024-03-06 DOI: 10.1002/tax.13156
Ali Mohammed Alzahrani, Joana Magos Brehm, Shahina A. Ghazanfar, Nigel Maxted
Verbascum and Rhabdotosperma are members of the family Scrophulariaceae. The first genus comprises approximately 360 species from almost all parts of the world, while the second contains a total of 8 species from tropical Africa and the Arabian Peninsula. Since 1977, the relationships between Verbascum and Rhabdotosperma continue to be contested. The present study aims to present the phylogenetic relationships and status among Verbascum species in the Arabian Peninsula. For phylogenetic analyses, maximum parsimony and Bayesian inference were performed. In total, 236 DNA sequences from 59 specimens of Arabian Verbascum were analysed. The phylogenetic analysis of one nuclear (ITS) and three chloroplastic (rbcL, matK, trnL) markers confirmed the monophyly of Verbascum, including the genus Rhabdotosperma. In addition to presenting novel phylogenetic relationships among the different Verbascum species in the Arabian Peninsula, our study reduced the species count of Arabian Verbascum to 16. Moreover, the phylogenetic analysis strongly supports the reinstatement of the genus Rhabdotosperma into Verbascum based on the Bayesian and maximum parsimony analyses.
马鞭草属(Verbascum)和鼠尾草属(Rhabdotosperma)均为景天科(Scrophulariaceae)植物。第一个属包括来自世界各地的约 360 个物种,第二个属则包括来自热带非洲和阿拉伯半岛的共 8 个物种。自 1977 年以来,Verbascum 和 Rhabdotosperma 之间的关系一直存在争议。本研究旨在介绍阿拉伯半岛马鞭草物种之间的系统发育关系和地位。系统发生分析采用了最大解析法和贝叶斯推断法。共分析了来自 59 个阿拉伯马鞭草标本的 236 个 DNA 序列。对一个核标记(ITS)和三个叶绿体标记(rbcL、matK、trnL)的系统进化分析证实了马鞭草的单系性,包括Rhabdotosperma属。我们的研究不仅揭示了阿拉伯半岛不同马鞭草物种之间新的系统发育关系,还将阿拉伯马鞭草的物种数量减少到 16 个。此外,根据贝叶斯分析和最大解析分析,系统发生分析强烈支持将 Rhabdotosperma 属重新归入马鞭草属。
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引用次数: 0
Report of the General Committee: 29 总务委员会的报告:29
IF 3.4 2区 生物学 Q2 EVOLUTIONARY BIOLOGY Pub Date : 2024-03-06 DOI: 10.1002/tax.13151
Karen L. Wilson
SummaryDecisions of the General Committee are reported on proposals and requests in Report 74 of the Permanent Nomenclature Committee for Vascular Plants and on two older proposals: 2550 (Plagiomnium) and 2786 (Ipomoea). The General Committee has approved the list of institutional votes for the Nomenclature Section of the XX International Botanical Congress in Madrid.
摘要报告了总务委员会关于维管束植物常设命名委员会第 74 号报告中的提案和请求以及两项旧提案的决定:2550(Plagiomnium)和 2786(Ipomoea)。总务委员会批准了马德里第二十届国际植物学大会命名科的机构投票名单。
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引用次数: 0
(3019) Proposal to conserve the name Hypericum olympicum (Hypericaceae) with a conserved type (3019) 关于保留类型的金丝桃(金丝桃科)名称的建议
IF 3.4 2区 生物学 Q2 EVOLUTIONARY BIOLOGY Pub Date : 2024-03-01 DOI: 10.1002/tax.13152
P. Pablo Ferrer-Gallego, Inmaculada Ferrando-Pardo, Maja Lazarević
<p>(3019) <b><i>Hypericum olympicum</i></b> L., Sp. Pl.: 784. 1 Mai 1753 [Angiosp.: <i>Guttif</i>. / <i>Hyperic</i>.], nom. cons. prop.</p><p>Typus: Herb. Clifford: 380, <i>Hypericum</i> No. 8 (BM barcode BM000646814), typ. cons. prop.</p><p><i>Hypericum olympicum</i> L. (Sp. Pl.: 784. 1753) (<i>H</i>. sect. <i>Olympia</i> (Spach) Nyman) is a small perennial herb distributed in the Balkan Peninsula (southeastern Serbia, Macedonia, Albania, Bulgaria, Greece [excluding Crete and western Aegean islands] and northwestern Turkey [Jordanov & Kožukharov in Jordanov, Fl. R. P. Bulg. 4: 235, t. 44, fig. 1. 1970; Greuter & al. in Med.-Checklist 3: 270. 1986; Robson & Strid in Strid, Mtn. Fl. Greece 1: 597, fig. 35. 1986; Qosja & al., Fl. Shquip. 2: 296, fig. 550. 1992; Zlatković in Stevanović & Niketić, Fl. Serbia 3: 311–313, 317, t. 53, fig. 1. 2022; POWO, 2023: https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:433682-1]). <i>Hypericum olympicum</i> is a variable species, but the variation, though partly geographical, is more or less continuous. In order to make this variation comprehensible, the species was divided into five forms, which remain distinct in cultivation (Robson in Plantsman 1: 193–200. 1980, in Phytotaxa 4: 26. 2010). Moreover, there are several ornamental cultivars of <i>H</i>. <i>olympicum</i> (e.g., ‘Citrinum’, ‘Sulphureum’, ‘Variegatum’) (see https://ecuador.inaturalist.org/taxa/567176-Hypericum-olympicum#cite_note-30).</p><p>Aerial parts of the plant are used in folk medicine for stomach ache, inflamed wounds and cuts (Tuzlacı & al. in Fitoterapia 72: 323–343. 2001), thus its essential oil composition (Gudžić & al. in Flavour Fragr. J. 16: 201–203. 2001; Smelcerovic & al. in Biochem. Syst. Ecol. 35: 99–113. 2007) and antimicrobial properties have been frequently investigated (Ilieva & al. in Plants (Switzerland) 12: 1500. 2023; Kirci & al. in J. Res. Pharm. 27: 2153–2159. 2023).</p><p>Linnaeus (l.c.) described <i>Hypericum olympicum</i> providing a short diagnosis “HYPERICUM floribus trigynis, calycibus acutis, staminibus corolla brevioribus, caule fruticoso” taken from Linnaeus (Hort. Cliff.: 380. 1738) and Van Royen (Fl. Leyd. Prodr.: 473 [not “374”]. 1740), followed by two synonyms: (1) “Hypericum montis olympi” cited from Wheeler [Sir George Wheler 1651–1724] (A Journey into Greece: 222. 1682) and Dillenius (Hort. Eltham.: 182, t. 151, fig. 183. 1732); and (2) “Ascyrum magno flore” cited from Bauhin (Prodr.: 130. 1620; Pinax: 280. 1623), and finally the reference “<i>Burs. XVI</i>: 25”. The protologue also included information about the origin of the species, “<i>Habitat in</i> Pyrenaeis, Olympo”. The references quoted by Linnaeus (Wheeler, l.c.: 221, lib. III, fig. III; Dillenius, l.c.: t. 151, fig. 183) include the illustrations “Hypericon montis Oly[m]pii foliis hursutis” (image available at https://www.alamy.com/stock-image-hypericon-montis-olympi-wheler-george-1682-16333079
(3019) Hypericum olympicum L., Sp.Pl.: 784.1 Mai 1753 [Angiosp. Guttif:Herb.Clifford: 380, Hypericum No. 8 (BM barcode BM000646814), typ.Olympia(Spach)Nyman)是一种多年生小型草本植物,分布于巴尔干半岛(塞尔维亚东南部、马其顿、阿尔巴尼亚、保加利亚、希腊[不包括克里特岛和爱琴海西部岛屿]和土耳其西北部[Jordanov &amp; Kožukharov in Jordanov, Fl. R. P. Bulg.R. P. Bulg.4: 235, t. 44, fig.1970; Greuter &amp; al. in Med.-Checklist 3: 270.1986; Robson &amp; Strid in Strid, Mtn.Fl.希腊 1: 597, 图 35.1986; Qosja &amp; al.Shquip.2:296,图 550。1992; Zlatković in Stevanović &amp; Niketić, Fl.塞尔维亚 3: 311-313, 317, t. 53, fig.2022; powo, 2023: https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:433682-1]).奥林匹亚金丝桃是一个易变种,但这种变异虽然部分是地理上的,但或多或少是连续的。1980 年,罗布森在《植物人》1:193-200 中,《植物志》4:26。2010 年)。此外,奥林帕克还有几种观赏栽培品种(如'Citrinum'、'Sulphureum'、'Variegatum')(见 https://ecuador.inaturalist.org/taxa/567176-Hypericum-olympicum#cite_note-30)。该植物的气生部分在民间用于治疗胃痛、发炎的伤口和割伤(Tuzlacı &amp; al. in Fitoterapia 72: 323-343. 2001),因此其精油成分(Gudžić &amp; al. in Flavour Fragr.J. 16: 201-203.2001; Smelcerovic &amp; al. in Biochem.Syst.Ecol.35: 99-113.2007),抗菌特性也经常被研究(Ilieva &amp; al. in Plants (Switzerland) 12: 1500.2023; Kirci &amp; al. in J. Res.27: 2153-2159.1738) 和 Van Royen (Fl. Leyd. Prodr.: 473 [not "374"]. 1740) 的简短诊断 "HYPERICUM floribus trigynis, calycibus acutis, staminibus corolla brevioribus, caule fruticoso"。1740),之后是两个同义词:(1) "Hypericum montis olympi",引自 Wheeler [George Wheler 爵士 1651-1724] (A Journey into Greece: 222. 1682) 和 Dillenius (Hort. Eltham.: 182, t. 151, fig. 183. 1732);(2) "Ascyrum magno flore",引自 Bauhin (Prodr.: 130. 1620; Pinax: 280. 1623),最后是 "Burs.XVI: 25"。原始描述还包括该物种的起源信息,"Habitat in Pyrenaeis, Olympo"。林奈引用的参考文献(Wheeler, l.c.: 221, lib. III, fig. III; Dillenius, l.c.: t. 151, fig. 183)包括插图 "Hypericon montis Oly[m]pii foliis hursutis"(图片见 https://www.alamy.com/stock-image-hypericon-montis-olympi-wheler-george-1682-163330790.html)和 "Hyper.根据 Jarvis (Order out of Chaos: 583. 2007) 的说法,Robson (in Notes Roy. Bot. Gard. Edinburgh 27: 199. 1967) 将保存在 BM 的 Clifford Herbarium 中的原始标本指定为 "ectotype"(Herb. Clifford: 380, Hypericum 8)。然而,罗布森(1967 年 l.c.)只提到 "奥林匹亚亚种(Subsp. olympicum)不同于高大直立的大花形式,如来自比西尼亚奥林匹亚山(Uludaǧ)的模式标本所代表的形式[...]"(古米西亚或比西尼亚奥林匹亚山是土耳其布尔萨省的一座山)。另一方面,Robson(l.c. 2010: 24)指出该名称的 "类型 "为:"类型:土耳其,布尔萨,'crescit in Olympo Asiae monte',未注明日期(花期),Herb.Cliff.380/8 (BM!-holotype)" 。该标本目前在 BM 的条形码为 BM000646814(图像可在 https://data.nhm.ac.uk/object/5b6258b8-1d4c-442f-b5e7-ef9ae221658f/1708387200000 上获取)。然而,Robson(l.c. 1967)的 "模式标本 "并不有效,因为没有按照 ICN 第 7.11 条的要求清楚地标明模式要素(Turland &amp.7.11 (Turland &amp; al. in Regnum Veg. 159. 2018)。罗布森的声明只提到了地点,却没有提到标本馆、作者、年份等其他信息,因此无法在罗布森的短语与保存在 BM 的克利福德标本馆中的林奈原始材料之间建立直接或间接的关系。根据第 7.11 条和第 9.23 条,罗布森(2010 年前)的 "类型化 "也是无效的。7.11 和 9.23 条的规定,"分型 "也是无效的,因为分型说明中不包括 "lectotype "一词(见第 9.23 条;第 9.10 条不适用)和 "designated here"(hic designatus)或等同词(第 7.11 条)。XVI: 25"。林奈在原典中明确引用了 "Burs.XVI: 25",这一引用与约阿希姆-布尔瑟(Joachim Burser)的《Hortus Siccus XVI: 25》中的一个标本一致,该标本目前保存在 UPS-BURSER。因此,尽管罗布森(l.
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