Cited by 26Chromosomal and Genetic VariationsPlant Diversity and EvolutionPlant Taxonomy and Phylogenetics

Rapid homoploid hybrid speciation in British gardens: The origin of Oxford ragwort (Senecio squalidus)

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Nevado, Bruno, Harris, Stephen A., Beaumont, Mark A., Hiscock, Simon J.·2020·Molecular Ecology

Abstract

Hybridisation can lead to homoploid hybrid speciation, i.e., the origin of new species without change in chromosome number between parents and offspring. Central to homoploid hybrid speciation is the role of hybridisation in the establishment of reproductive isolation between the hybrid and the parental species in the early stages of speciation, when typically all species occur at least partly in sympatry. In this work we analyse genome‐wide polymorphism data obtained by transcriptome sequencing of the British hybrid species Oxford ragwort (Senecio squalidus,Asteraceae), its two Italian parental species (S. aethnensis and S. chrysanthemifolius)and their naturally occurring hybrids on Mt Etna (Italy). We show that Oxford ragwort most likely originated from de novo hybridisation between its two Italian parental species whilst they were in cultivation in British gardens at the turn of the 18th century. Reproductive isolation between the new hybrid species and its parental species probably resulted from inheritance of genetic incompatibilities between the two parental species and subsequent ecological segregation – both of which have been shown in previous studies. Our results imply that S. squalidus meets the most stringent criteria set forth to identify homoploid hybrid speciation, and call attention to the creative role of hybridisation in responding to novel environmental conditions.

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  • Other examples come from studies of adaptive introgression or homoploid hybrid speciation, in which alleles or SVs critical to RI have been identified in parental populations.

    “Other examples come from studies of adaptive introgression or homoploid hybrid speciation (see Speciation with gene flow, introgression, and hybrid speciation), in which alleles or SVs critical to RI have been identified in parental populations (Nevado et al., 2020; Todesco et al., 2020; Wang et al., 2021b).”

    From Genomics of plant speciation (2023) · cites this paper as Nevado et al., 2020

    The Introduction and Discussion (§4.2; page numbers unavailable) support Oxford ragwort as an example of homoploid hybrid speciation and discuss inherited genetic incompatibilities as a possible basis for reproductive isolation. But §4.2 explicitly says this study does not address the mechanism of isolation; it does not identify particular alleles or structural variants critical to it in the parental populations. (LLM, conf=0.88)

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Research works printed but not linked: 5

  1. [21]21. Druce, G. C. (1927). The flora of Oxfordshire (2nd ed.). Clarendon Press.
  2. [25]25. Haas, B. J., Papanicolaou, A., Yassour, M., Grabherr, M., Blood, P. D., Bowden, J., Couger, M. B., Eccles, D., Li, B., Lieber, M., & Regev, A. (2013). De novo transcript sequence reconstruction from RNA-Seq: Reference generation and analysis with Trinity. Nature Protocols, 8(8). https://doi.org/10.1038/nprot.2013.1084 · DOI
  3. [32]32. Kent, D. H. (1956). Senecio squalidus L. in the British Isles. 1. Early records (to 1877). Proceedings of the Botanical Society of the British Isles, 2, 115-118.
  4. [33]33. Kent, D. H. (1960). Senecio squalidus L. in the British Isles. 2. The spread from Oxford (1879-1939). Proceedings of the Botanical Society of the British Isles, 3, 375-379.
  5. [52]52. Ross, R. I. C. (2010). Local adaptation and adaptive divergence in a hybrid species complex in Senecio. Doctor of Philosophy PhD, University of Oxford.

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  • Genomics of plant speciation

    Bock, D. G., Cai, Z., Elphinstone, C., González-Segovia, E., Hirabayashi, K., Huang, K., Keais, G. L., Kim, A., Owens, G. L., & Rieseberg, L. H. (2023) · Plant Communications · doi:10.1016/j.xplc.2023.100599 · Cited by 84 · see citing works

    “…genomic studies have confirmed the hybrid origin of the Oxford ragwort (Senecio squalidus) from the two Senecio species on Mt. Etna described above (Nevado et al., 2020), identified several potential new cases of homoploid hybrid speciation (e.g., Gr€unig et al., 2021; Wang et al., 2021b; Wang et…”
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Authors
Nevado, B., Harris, S. A., Beaumont, M. A., & Hiscock, S. J.
Affiliations
  • University of Oxford (GB)
  • University of Bristol (GB)
Corresponding author
Nevado, Bruno
Venue
Molecular Ecology
Publisher
Wiley
Published
2020-09-26
Volume
29
Issue
21
Pages
4221-4233
ISSN
  • 0962-1083 (ISSN-L)
  • 1365-294X
OpenAlex
W3086640053
Cited by
26
References
54
Citations by year
2025: 7 · 2024: 4 · 2023: 6 · 2022: 6 · 2021: 2 · 2020: 1
FWCI
2.42
Type
journal article
Language
en
Open access
Locations
  • Molecular Ecology (publishedVersion)
  • PubMed (publishedVersion)
  • Explore Bristol Research (publishedVersion)
  • Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) (submittedVersion, other-oa)
  • Bristol Research (University of Bristol) (submittedVersion)
Funders
John Fell Fund, University of Oxford (162/091)
Topics
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Chromosomal and Genetic Variations
  • Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Plant Diversity and Evolution
  • Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Plant Taxonomy and Phylogenetics
Keywords
homoploid hybrid speciation, Senecio squalidus, hybridization, reproductive isolation, genetic incompatibility, ecological segregation, garden plants, Mount Etna, Asteraceae, genome-wide polymorphism
MeSH terms
Gardens, Hybridization, Genetic, Italy, Senecio, Genetic Speciation

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