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Species limits and relationships within Otidea inferred from multiple gene phylogenies

机译:从多个基因系统学推断的Otidea内的物种限制和关系

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摘要

The genus Otidea is one of the more conspicuous members of the Pyronemataceae, with high species diversity in hemiboreal and boreal forests. The genus is morphologically coherent and in previous higher-level multi-gene analyses it formed a highly supported monophyletic group. Species delimitation within Otidea is controversial and much confusion has prevailed in the naming of taxa. To provide a phylogenetic hypothesis of Otidea, elucidate species diversity and limits we compiled a four-gene dataset including the nuclear LSU rDNA and three nuclear protein-coding genes (RPB1, RPB2 and EF-1α) for 89 specimens (total 4 877 nucleotides). These were selected from a larger sample of material studied using morphology and 146 ITS (ITS1-5.8S-ITS2) and 168 LSU rDNA sequences to represent the full genetic diversity. Using genealogical concordance phylogenetic species recognition (GCPSR), Bayesian and maximum likelihood analyses of the individual datasets resolved 25 species of Otidea. An additional eight singletons are considered to be distinct species, because they were genetically divergent from their sisters. Sequences of multiple genes were included from 13 holotypes, one neotype and three epitypes. Otidea angusta, O. myosotis and O. papillata f. pallidefurfuracea are nested within O. nannfeldtii, O. leporina and O. tuomikoskii, respectively and are considered synonyms. Otidea cantharella var. minor is shown to be a distinct species. Five new species were discovered: O. oregonensis and O. pseudoleporina for North America; and O. borealis, O. brunneoparva and O. subformicarum for Europe. The analyses of the individual four gene datasets yielded phylogenies that were highly concordant topologically, except for the RPB1 that showed supported conflict for some nodes in Bayesian analysis. Excluding the RPB1 from the combined analyses produced an identical topology to the four-gene phylogeny, but with higher support for several basal nodes and lower support for several shallow nodes. We argue to use the three-gene dataset to retrieve the maximum support for the higher-level relationships in Otidea, but still utilise the signal from the RPB1 for the delimitation and relationships of closely related species. From the four gene regions utilised, EF-1α and RPB1 have the strongest species recognition power, and with higher amplification success EF-1α may serve as the best secondary barcoding locus for Otidea (with ITS being a primary). The phylogeny from the three- and four-gene datasets is fully resolved and strongly supported in all branches but one. Two major clades, as part of six inclusive clades A–F, are identified – and ten subclades within these: A) O. platyspora and O. alutacea subclades, and B) O. papillata, O. leporina, O. tuomikoskii, O. cantharella, O. formicarum, O. unicisa, O. bufonia-onotica and O. concinna subclades. Morphological features in Otidea appear to be fast evolving and prone to shifts, and are poor indicators of higher-level relationships. Nevertheless, a conspicuous spore ornament is a synapomorphy for the O. unicisa subclade (/Otideopsis); all other species in Otidea have smooth or verruculose (in SEM) spores. Exclusively pale to bright yellow apothecia and straight to curved, broadly clavate to distinctly capitate paraphyses are synapomorphies for a restricted O. concinna subclade (/Flavoscypha). The curved to hooked apices of the paraphyses is suggested to be a symplesiomorphic trait for the genus. The reaction of resinous exudates on the outermost excipular cells that coalesce into amber drops in Melzer’s reagent is likely an ancestral state for clade B. We estimate that Otidea consists of 47 species worldwide, based on all available information (including morphology, ITS or LSU sequences, and literature descriptions). Three fifths of the species occur in Europe, with 20 species recognised as endemic. At least 14 species occur in North America and 17 in Asia, with eight and ten species considered endemic to each continent, respectively. Our knowledge about Otidea in Asia is still fragmentary and the diversity likely much higher.
机译:Otidea属是pyyomamataceae的最明显的成员之一,在半实体和北方森林中具有较高的物种多样性。该属在形态上是连贯的,在以前的高级多基因分析中,它形成了高度支持的单系群体。 Otidea内的物种划定是有争议的,在分类单元的命名中普遍存在很多混乱。为了提供Otidea的系统发育假说,阐明物种多样性和局限性,我们针对89个标本(总共4 877个核苷酸)编制了包括核LSU rDNA和三个核蛋白编码基因(RPB1,RPB2和EF-1α)的四基因数据集。 。这些是从使用形态学和146 ITS(ITS1-5.8S-ITS2)和168 LSU rDNA序列研究的较大材料样本中选择的,代表了完整的遗传多样性。使用族谱一致性系统发生种识别(GCPSR),单个数据集的贝叶斯和最大似然分析可解析25种Otidea。另外八个单胎被认为是不同的物种,因为它们在遗传上不同于其姐妹。包括13种全基因型,一种新基因型和三种表型的多个基因的序列。 Otidea angusta,O。myosotis和O. papillata f。 pallidefurfuracea分别嵌套在O. nannfeldtii,O。leporina和O. tuomikoskii中,并被视为同义词。 Otidea cantharella var。未成年人被证明是一个独特的物种。发现了五个新物种:北美的O. oregonensis和假单孢菌;和 O。北极虫 O。 brunneoparva O。欧洲的subformicarum 。对单个四个基因数据集的分析得出的系统发育在拓扑上高度一致,除了RPB1在贝叶斯分析中对某些节点显示了支持的冲突之外。从组合分析中排除RPB1会产生与四基因系统发育相同的拓扑,但对几个基节点的支持较高,而对几个浅节点的支持较低。我们认为要使用三基因数据集来检索对 Otidea 中更高级别关系的最大支持,但仍要使用RPB1的信号来确定紧密相关物种的关系。在利用的四个基因区域中,EF-1α和RPB1具有最强的物种识别能力,并且具有较高的扩增成功率,EF-1α可能是 Otidea 的最佳二级条形码编码位点(其中ITS为主要)。三基因和四基因数据集的系统发育已得到完全解决,除一个分支外的所有分支均得到了大力支持。确定了两个主要进化枝,作为六个包含性进化枝A–F的一部分–以及其中的十个子进化枝:A)O。 platyspora O。 Alutacea 小节,B) O。乳头 O。 leporina O。 tuomikoskii O。 Cantharella O。 formicarum O。 unicisa O。紫花苜蓿 O。 concinna 小节。凤蝶的形态特征似乎发展迅速且容易发生变化,并且是高层关系的较差指标。然而,明显的孢子装饰物是 O的一个突触。 unicisa 小节(/ Otideopsis ); Otidea 中的所有其他物种都具有光滑的或疣状的(在SEM中)孢子。完全苍白至鲜黄色的紫红色,和直到弯曲,宽棒状到明显头状的附生植物是限制的 O的同形。 concinna 小节(/ Flavoscypha )。拟南芥属的弯曲到钩状的顶点被认为是该属的一种同形特征。树脂分泌物在梅尔泽试剂中聚集成琥珀滴的最外层细胞上的反应可能是进化枝B的祖先状态。根据所有可用信息,我们估计 Otidea 由全世界47个种组成(包括形态,ITS或LSU序列以及文献描述)。该物种的五分之三发生在欧洲,其中20种被认为是特有的。在北美至少有14种,在亚洲至少有17种,每个大陆分别有8种和10种。我们对亚洲的 Otidea 的了解仍然是零碎的,而且多样性可能更高。

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