Affiliations 

  • 1 International Center for Tropical Botany at the Kampong, Institute of Environment, Florida International University, Miami, FL 33133
  • 2 Natural History Museum of Denmark, University of Copenhagen, 1123 Copenhagen, Denmark
  • 3 Singapore Botanic Gardens, National Parks Board, 259569, Singapore
  • 4 Thailand National History Museum, National Science Museum, Klong Luang, Pathum Thani 12120, Thailand
  • 5 Department of Biology, The College of New Jersey, Ewing, NJ 08618
  • 6 Sarawak Forestry Corporation, 93250 Kuching, Sarawak, Malaysia
  • 7 CIFOR-ICRAF, St Eugene Office Park, 10101 Lusaka, Zambia
  • 8 The Morton Arboretum, Lisle, IL 60532
  • 9 CEFE, CNRS, Université de Montpellier, EPHE, IRD, 34090 Montpellier, France
  • 10 Instituto de Pesquisa do Jardim Botânico do Rio de Janeiro, Diretoria de Pesquisa Científica, 22460-030 Rio de Janeiro-RJ, Brazil
  • 11 Chinese Academy of Sciences, Key Laboratory of Tropical Forest Ecology, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences, 666303 Mengla, China
  • 12 Sabah Forest Research Centre, Sabah Forestry Department, 90175 Sandakan, Sabah, Malaysia
  • 13 Borneo Research Consultants, W3 0HA London, United Kingdom
  • 14 Faculty of Agriculture & Applied Sciences, i-CATS University College, 93350 Kuching, Sarawak, Malaysia
  • 15 CBGP, INRAE, CIRAD, IRD, Montpellier SupAgro, Université de Montpellier, 34988 Montpellier, France
  • 16 Sarawak Forest Department, 34988 Kuching, Sarawak, Malaysia
  • 17 Bell Museum, University of Minnesota, St. Paul, MN 55113
  • 18 Plant Biology and Conservation, Northwestern University, Evanston, IL 60208
  • 19 State Key Laboratory of Systematic and Evolutionary Botany, Institute of Botany, Chinese Academy of Sciences, 100093 Beijing, China
  • 20 School of Life Sciences, East China Normal University, 200241 Shanghai, China
  • 21 National Tropical Botanical Garden, Kalāheo, HI 96741
Proc Natl Acad Sci U S A, 2023 Jul 11;120(28):e2222035120.
PMID: 37399402 DOI: 10.1073/pnas.2222035120

Abstract

Studies investigating the evolution of flowering plants have long focused on isolating mechanisms such as pollinator specificity. Some recent studies have proposed a role for introgressive hybridization between species, recognizing that isolating processes such as pollinator specialization may not be complete barriers to hybridization. Occasional hybridization may therefore lead to distinct yet reproductively connected lineages. We investigate the balance between introgression and reproductive isolation in a diverse clade using a densely sampled phylogenomic study of fig trees (Ficus, Moraceae). Codiversification with specialized pollinating wasps (Agaonidae) is recognized as a major engine of fig diversity, leading to about 850 species. Nevertheless, some studies have focused on the importance of hybridization in Ficus, highlighting the consequences of pollinator sharing. Here, we employ dense taxon sampling (520 species) throughout Moraceae and 1,751 loci to investigate phylogenetic relationships and the prevalence of introgression among species throughout the history of Ficus. We present a well-resolved phylogenomic backbone for Ficus, providing a solid foundation for an updated classification. Our results paint a picture of phylogenetically stable evolution within lineages punctuated by occasional local introgression events likely mediated by local pollinator sharing, illustrated by clear cases of cytoplasmic introgression that have been nearly drowned out of the nuclear genome through subsequent lineage fidelity. The phylogenetic history of figs thus highlights that while hybridization is an important process in plant evolution, the mere ability of species to hybridize locally does not necessarily translate into ongoing introgression between distant lineages, particularly in the presence of obligate plant-pollinator relationships.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.