Department of Biology, Washington University in Saint Louis, St. Louis, MO 63130, USA.
School of Plant Sciences and Food Security, Faculty of Life Sciences, Tel Aviv University, Tel Aviv 6997820, Israel.
Curr Biol. 2024 Jul 22;34(14):R697-R707. doi: 10.1016/j.cub.2024.05.029.
The evolution of the land plant alternation of generations has been an open question for the past 150 years. Two hypotheses have dominated the discussion: the antithetic hypothesis, which posits that the diploid sporophyte generation arose de novo and gradually increased in complexity, and the homologous hypothesis, which holds that land plant ancestors had independently living sporophytes and haploid gametophytes of similar complexity. Changes in ploidy levels were unknown to early researchers. The antithetic hypothesis is contradicted by generation cycles in Lower Devonian Rhynie chert plants, whose sporophytes and gametophytes have similar morphologies and by some Silurian sporophytes whose complexity exceeds that of Rhynie chert sporophytes. The oldest unambiguous bryophyte gametophytes (thalli) are from the upper Middle Devonian, with an unconnected sporophyte nearby. Based on the 2024 discovery that conjugate algae are paraphyletic to land plants, we present a new hypothesis for the evolution of the land plant generation cycle, focusing on labile ploidy levels and types of reproduction found in conjugate algae. Our 'sexual lability' hypothesis assumes a period of unstable generation cycles (as regards ploidy), likely with predominant clonal growth, as is common in conjugate algae, resulting in sporophytes and gametophytes of similar morphology. When sexual reproduction became stabilized, the timing of gamete fusion, meiosis, and resistant wall formation, which are heterochronic in some conjugate algae, became standardized, with wall formation permanently delayed. In our scenario, independently living adult sporophytes are the land plant ancestral condition, and life-long sporophyte retention on the gametophyte is a bryophyte apomorphy.
陆地植物世代交替的演化在过去的 150 年中一直是一个悬而未决的问题。有两个假说一直占据着讨论的主导地位:对偶假说,该假说认为二倍体孢子体世代是全新出现的,并逐渐变得更加复杂;以及同源假说,该假说认为陆地植物的祖先是具有独立生活的孢子体和相似复杂性的单倍体配子体。早期的研究人员并不知道倍性水平的变化。对偶假说与下泥盆纪 Rhynie 硅化木植物的世代循环相矛盾,这些植物的孢子体和配子体具有相似的形态,还有一些志留纪的孢子体比 Rhynie 硅化木的孢子体更加复杂。最古老的明确无误的苔藓植物配子体(叶状体)来自上中泥盆纪,附近有一个不相连的孢子体。基于 2024 年发现的共轭藻类是陆地植物的并系群,我们提出了一个陆地植物世代循环演化的新假说,重点关注共轭藻类中发现的不稳定倍性水平和繁殖类型。我们的“性变异性”假说假设存在不稳定的世代循环(关于倍性)时期,可能以无性克隆生长为主,这在共轭藻类中很常见,导致孢子体和配子体具有相似的形态。当有性繁殖变得稳定时,配子融合、减数分裂和抗性壁形成的时间(在某些共轭藻类中是异时的)变得标准化,壁形成永久延迟。在我们的设想中,独立生活的成年孢子体是陆地植物的原始条件,终身保留孢子体是苔藓植物的一个特化性状。