Interrogating Phylogenetic Discordance Resolves Deep Splits in the Rapid Radiation of Old World Fruit Bats (Chiroptera: Pteropodidae)

Author:

Nesi Nicolas1,Tsagkogeorga Georgia1,Tsang Susan M23,Nicolas Violaine4,Lalis Aude4,Scanlon Annette T5,Riesle-Sbarbaro Silke A678,Wiantoro Sigit9,Hitch Alan T10,Juste Javier11,Pinzari Corinna A12,Bonaccorso Frank J13,Todd Christopher M14,Lim Burton K15,Simmons Nancy B2,McGowen Michael R16,Rossiter Stephen J1

Affiliation:

1. School of Biological and Chemical Sciences, Queen Mary University of London, Mile End Road, London E1 4NS, UK

2. Department of Mammalogy, Division of Vertebrate Zoology, American Museum of Natural History, New York, USA

3. Zoology Section, National Museum of Natural History, Manila, Philippines

4. Institut de Systématique, Evolution, Biodiversité (ISYEB), Muséum national d’Histoire naturelle, CNRS, Sorbonne Université, EPHE, Université des Antilles, Paris, France

5. School of Natural and Built Environments, University of South Australia, Mawson Lakes, SA, Australia

6. Department of Veterinary Medicine, University of Cambridge, Cambridge, UK

7. Institute of Zoology, Zoological Society of London, London, UK

8. Centre for Biological Threats and Special Pathogens, Robert Koch Institute, Berlin, Germany

9. Museum Zoologicum Bogoriense, Research Center for Biology, Indonesian Institute of Sciences, Cibinong, Indonesia

10. Department of Wildlife, Fish, and Conservation Biology, University of California Davis, CA, USA

11. Estación Biológica de Doñana (CSIC), Avda. Américo Vespucio, Sevilla, Spain

12. University of Hawaii at Hilo, Hawaii, USA

13. PO Box 417, Volcano, Hawaii, USA

14. The Hawkesbury institute for the Environment, Western Sydney University, Australia

15. Royal Ontario Museum, Toronto, ON M5S 2C6, Canada

16. Department of Vertebrate Zoology, Smithsonian National Museum of Natural History, Washington, DC, USA

Abstract

Abstract The family Pteropodidae (Old World fruit bats) comprises $>$200 species distributed across the Old World tropics and subtropics. Most pteropodids feed on fruit, suggesting an early origin of frugivory, although several lineages have shifted to nectar-based diets. Pteropodids are of exceptional conservation concern with $>$50% of species considered threatened, yet the systematics of this group has long been debated, with uncertainty surrounding early splits attributed to an ancient rapid diversification. Resolving the relationships among the main pteropodid lineages is essential if we are to fully understand their evolutionary distinctiveness, and the extent to which these bats have transitioned to nectar-feeding. Here we generated orthologous sequences for $>$1400 nuclear protein-coding genes (2.8 million base pairs) across 114 species from 43 genera of Old World fruit bats (57% and 96% of extant species- and genus-level diversity, respectively), and combined phylogenomic inference with filtering by information content to resolve systematic relationships among the major lineages. Concatenation and coalescent-based methods recovered three distinct backbone topologies that were not able to be reconciled by filtering via phylogenetic information content. Concordance analysis and gene genealogy interrogation show that one topology is consistently the best supported, and that observed phylogenetic conflicts arise from both gene tree error and deep incomplete lineage sorting. In addition to resolving long-standing inconsistencies in the reported relationships among major lineages, we show that Old World fruit bats have likely undergone at least seven independent dietary transitions from frugivory to nectarivory. Finally, we use this phylogeny to identify and describe one new genus. [Chiroptera; coalescence; concordance; incomplete lineage sorting; nectar feeder; species tree; target enrichment.]

Funder

European Union’s Horizon 2020

Marie Sklodowska-Curie

European Research Council Starting Grant

NMNH

Publisher

Oxford University Press (OUP)

Subject

Genetics,Ecology, Evolution, Behavior and Systematics

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