Journal of Systematics and Evolution ›› 2026, Vol. 64 ›› Issue (4): 776-792.DOI: 10.1111/jse.70073

所属专题: Virtual Focus on Systematics and Biodiversity Conservation

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  • 收稿日期:2025-10-09 接受日期:2026-03-08 出版日期:2026-07-01 发布日期:2026-07-13

Phylogenomics, species diversification, and biogeography of Dalbergia (Leguminosae) using hybrid capture of nuclear genes

Fabien Robert Rahaingoson1,2,3, Wei Gu1,2, Oyetola Oyebanji4, Shui-Yin Liu5, Qin Tian6, Jian Liu2,7, Gregory W. Stull8, Ryan A. Folk9, Jian Wang10,11, Douglas E. Soltis12,13, Pamela S. Soltis12, Ting-Shuang Yi1,2*, Rong Zhang1,2,14*   

  1. 1Germplasm Bank of Wild Species & Yunnan Key Laboratory of Crop Wild Relatives Omics, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China
    2University of the Chinese Academy of Sciences, Beijing 100049, China
    3Key Laboratory of Genetic Evolution & Animal Models, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming 650201, China
    4Botanical Research Institute of Texas, Fort Worth 76107, TX, USA
    5Shenzhen Branch, Guangdong Laboratory of Lingnan Modern Agriculture, Key Laboratory of Synthetic Biology, Ministry of Agriculture and Rural Affairs, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen 518000, China
    6Center for Interdisciplinary Biodiversity Research & College of Forestry, Shandong Agricultural University, Tai’an 271018, China
    7Yunnan Key Laboratory for Wild Plant Resources, Department of Economic Plants and Biotechnology, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China
    8Department of Botany, National Museum of Natural History, Smithsonian Institution, Washington, DC 20013, USA
    9Department of Biological Sciences, Mississippi State University, Starkville 39762, MS, USA
    10Department of the Environment, Queensland Herbarium & Biodiversity Science, Tourism, Science and Innovation, Brisbane Botanic Gardens, Brisbane, QLD 4066, Australia
    11Queensland Alliance for Agriculture and Food Innovation, The University of Queensland, St Lucia, QLD 4072, Australia
    12Florida Museum of Natural History, University of Florida, Gainesville 32611, FL, USA
    13Department of Biology, University of Florida, Gainesville 32611, FL, USA
    14Key Laboratory of Plant Diversity and Specialty Crops, Chinese Academy of Sciences, Beijing 100093, China
    Authors for correspondence. Ting-Shuang Yi. E-mail: tingshuangyi@mail.kib.ac.cn; Rong Zhang. E-mail: zhangronga@mail.kib.ac.cn
  • Received:2025-10-09 Accepted:2026-03-08 Online:2026-07-01 Published:2026-07-13
  • Supported by:
    This work was supported by grants from the Yunnan Fundamental Research Projects (202301AT070310), the National Natural Science Foundation of China (32270247), the Yunnan Revitalization Talent Support Program–Yunling Scholar Project (XDYC‐YLXZ‐2024‐0021), the Yunnan Revitalization Talent Support Program–Young Talent Program (XDYCQNRC‐2022‐0257), the Major Program for Basic Research Project of Yunnan Province (202401BC070001), the National Natural Science Foundation of China (key international (regional) cooperative research project (31720103903), and China Postdoctoral Science Foundation (2020M683391).

Abstract: Dalbergia (Leguminosae) is a pantropical genus that serves as an ideal system for studying pantropical biogeography and diversification. However, limited taxon sampling and molecular data have hindered the resolution of intrageneric relationships and understanding of its evolutionary history. Here, we reconstruct a densely sampled phylogeny of Dalbergia based on hybrid capture of 89 low-copy nuclear loci, including 98 species spanning all major biogeographic regions and most previously recognized taxonomic clades. Phylogenetic analyses using concatenated and coalescent approaches support the monophyly of Dalbergia and consistently identify six major clades, including a distinct and newly identified Africa-Madagascar lineage (clade E) with potential taxonomic significance. Our results propose merging two of its sections, sect. Dalbergia and sect. Selenolobium, and expanding sect. Ecastaphyllum to include some African species. Topological incongruences observed between concatenated and coalescent trees, together with the high gene tree conflict at certain nodes, are consistent with localized effects of hybridization and/or incomplete lineage sorting. Divergence dating and model-based biogeographic analyses support a Neotropical origin of Dalbergia in the middle Eocene (~39 Ma), followed by repeated long-distance dispersal events from Africa to Asia, Neotropics, and Madagascar, and back into the Neotropics. An early diversification burst in Africa during the late Oligocene–early Miocene (~27–18 Ma) preceded the genus′s intercontinental expansion. Diversification rates were high across all four regions, with Madagascar showing the highest speciation rate. These macroevolutionary dynamics coincided with Eocene–Miocene climatic changes and habit shifts. This study provides a robust phylogenetic framework for Dalbergia, refines its temporal and biogeographic history, and illustrates how dispersal, climatic change, and lineage-specific diversification have interacted to generate pantropical biodiversity.

Key words: Dalbergia, Hyb-Seq, long-distance dispersal, pantropical, phylogenetic relationships, phylogenomics