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()中的子囊盘祖先、进化与再进化。 (你提供的原文括号部分内容缺失,我只能按现有内容准确翻译)

Apothecial Ancestry, Evolution, and Re-Evolution in ().

作者信息

Quijada Luis, Matočec Neven, Kušan Ivana, Tanney Joey B, Johnston Peter R, Mešić Armin, Pfister Donald H

机构信息

Department of Organismic and Evolutionary Biology, The Farlow Reference Library and Herbarium of Cryptogamic Botany, Harvard University, 22 Divinity Avenue, Cambridge, MA 02138, USA.

Laboratory for Biological Diversity, Ruđer Bošković Institute, Bijenička Cesta 54, HR-10000 Zagreb, Croatia.

出版信息

Biology (Basel). 2022 Apr 11;11(4):583. doi: 10.3390/biology11040583.

Abstract

Closed cleistothecia-like ascomata have repeatedly evolved in non-related perithecioid and apothecioid lineages of lichenized and non-lichenized . The evolution of a closed, darkly pigmented ascoma that protects asci and ascospores is conceived as either an adaptation to harsh environmental conditions or a specialized dispersal strategy. Species with closed ascomata have mostly lost sterile hymenial elements (paraphyses) and the capacity to actively discharge ascospores. The class , one of the most speciose classes of , is mainly apothecioid, paraphysate, and possesses active ascospore discharge. Lineages with closed ascomata, and their morphological variants, have evolved independently in several families, such as , , , etc. is a distinctive order in the class. It has two widespread families (, ) with mostly closed ascomata, evanescent asci, and thus passively dispersed ascospores. Within the order, closed ascomata dominate and a great diversity of peridia have evolved as adaptations to different dispersal strategies. The type genus, , is an exceptional case of ascomatal evolution within the order. Its species are the most diverse in functional traits, encompassing species with closed ascomata and evanescent asci, and species with open ascomata, active ascospore discharge, and paraphyses. Open ascomata were previously suggested as the ancestral state in the genus, these ascomata depend on mammals and birds as dispersal agents. In this scheme, species with closed ascomata, a lack of paraphyses, and passive ascospore discharge exhibit derived traits that evolved in adaptation to cold ecosystems. Here, we used morphological and phylogenetic methods, as well as the reconstruction of ancestral traits for ascomatal type, asci dehiscence, the presence or absence of paraphyses, and ascospore features to explore evolution within . We demonstrate the apothecial ancestry in and propose a new hypothesis about the evolution of the open ascomata in , involving a process of re-evolution where the active dispersal of ascospores appears independently twice within the order. We propose a new family, , within , that retains the phenotypic features exhibited by species of , i.e., pigmented capitate paraphyses and active asci discharge with an opening limitation ring.

摘要

在地衣化和非地衣化的无关的囊壳状和盘状类群中,封闭的闭囊壳状子囊果已经多次进化。封闭的、颜色深的子囊果的进化,其作用是保护子囊和子囊孢子,这被认为要么是对恶劣环境条件的一种适应,要么是一种特殊的传播策略。具有封闭子囊果的物种大多失去了不育的子实层成分(侧丝)和主动释放子囊孢子的能力。该类群是最具物种多样性的类群之一,主要为盘状、具侧丝,并具有主动的子囊孢子释放。具有封闭子囊果及其形态变体的类群,在几个科中独立进化,如……等。……是该类群中一个独特的目。它有两个分布广泛的科(……),大多具有封闭的子囊果、易消失的子囊,因此子囊孢子是被动传播的。在这个目中,封闭的子囊果占主导地位,并且已经进化出了各种各样的包被,作为对不同传播策略的适应。模式属……是该目内子囊果进化的一个特殊例子。其物种在功能特征上最为多样,包括具有封闭子囊果和易消失子囊的物种,以及具有开放子囊果、主动子囊孢子释放和侧丝的物种。开放的子囊果以前被认为是该属的祖先状态,这些子囊果依赖哺乳动物和鸟类作为传播媒介。在这个模式中,具有封闭子囊果、缺乏侧丝和被动子囊孢子释放的物种表现出衍生特征,这些特征是为了适应寒冷生态系统而进化的。在这里,我们使用形态学和系统发育方法,以及对子囊果类型、子囊开裂、侧丝的有无和子囊孢子特征的祖先特征重建,来探索……内的进化。我们证明了……中的盘状祖先,并提出了一个关于……中开放子囊果进化的新假说,涉及一个重新进化的过程,其中子囊孢子的主动传播在该目内独立出现了两次。我们在……中提出了一个新科……,它保留了……物种所表现出的表型特征,即有色头状侧丝和带有开口限制环的主动子囊释放。

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