Simpson Lalita, Clements Mark A, Orel Harvey K, Crayn Darren M, Nargar Katharina
Australian Tropical Herbarium, James Cook University, Cairns, QLD, Australia.
College of Science and Engineering, James Cook University, Cairns, QLD, Australia.
Front Plant Sci. 2024 May 24;14:1219354. doi: 10.3389/fpls.2023.1219354. eCollection 2023.
The hyperdiverse orchid genus is the second largest genus of flowering plants and exhibits a pantropical distribution with a center of diversity in tropical Asia. The only section with a center of diversity in Australasia is sect. . However, the phylogenetic placement, interspecific relationships, and spatio-temporal evolution of this section remain largely unclear. To infer broad-level relationships within , and interspecific relationships within sect. , a genome skimming dataset was generated for 89 samples, which yielded 70 plastid coding regions and a nuclear ribosomal DNA cistron. For 18 additional samples, Sanger data from two plastid loci (K and 1) and nuclear ITS were added using a supermatrix approach. The study provided new insights into broad-level relationships in , including phylogenetic evidence for the non-monophyly of sections , , , , , , , , , and . Section and sect. formed a highly supported clade that was resolved as a sister group to the remainder of the genus. Divergence time estimations based on a relaxed molecular clock model placed the origin of in the Early Oligocene (ca. 33.2 Ma) and sect. in the Late Oligocene (ca. 23.6 Ma). Ancestral range estimations based on a BAYAREALIKE model identified the Australian continent as the ancestral area of the sect. The section underwent crown diversification from the mid-Miocene to the late Pleistocene, predominantly in continental Australia. At least two independent long-distance dispersal events were inferred eastward from the Australian continent to New Zealand and to New Caledonia from the early Pliocene onwards, likely mediated by predominantly westerly winds of the Southern hemisphere. Retraction and fragmentation of the eastern Australian rainforests from the early Miocene onwards are likely drivers of lineage divergence within sect. facilitating allopatric speciation.
高度多样化的兰花属是开花植物的第二大属,呈现泛热带分布,多样性中心在亚洲热带地区。在澳大拉西亚具有多样性中心的唯一亚组是亚组 。然而,该亚组的系统发育位置、种间关系以及时空演化在很大程度上仍不清楚。为了推断该属内的广泛关系以及该亚组内的种间关系,为89个样本生成了一个基因组浅层测序数据集,产生了70个叶绿体编码区和一个核糖体DNA顺反子。对于另外18个样本,使用超级矩阵方法添加了来自两个叶绿体基因座(K和1)和核ITS的桑格数据。该研究为该属的广泛关系提供了新的见解,包括亚组 、 、 、 、 、 、 、 、 和 非单系性的系统发育证据。亚组 和亚组 形成了一个得到高度支持的分支,被解析为该属其余部分的姐妹群。基于宽松分子钟模型的分歧时间估计将该属的起源置于渐新世早期(约3320万年前),亚组 的起源置于渐新世晚期(约2360万年前)。基于BAYAREALIKE模型的祖先分布估计确定澳大利亚大陆是该亚组的祖先区域。该亚组从中新世中期到晚更新世经历了冠部多样化,主要发生在澳大利亚大陆。从上新世早期开始,至少有两次独立的长距离扩散事件被推断从澳大利亚大陆向东扩散到新西兰和新喀里多尼亚,可能主要由南半球的西风介导。从渐新世早期开始,澳大利亚东部雨林的退缩和破碎化可能是该亚组内谱系分歧的驱动因素,促进了异域物种形成。