Homoploid hybrid speciation is the origin of a hybrid species without change in chromosome number. Although currently thought to be a rare form of speciation, especially relative to the more common allopolyploid hybrid speciation, it is feasible that many examples of homoploid hybrid species will be discovered in the future now that genetic resources are readily available for testing their occurrence. In this review, we focus on the speed of homoploid hybrid speciation, the importance of ecological and spatial isolation in the process, and the nature of genetic changes that occur in a new hybrid during its origin and establishment in the wild. With reference mainly to the extensive work carried out on homoploid hybrid species of Helianthus, and to our own work on the very recently originated diploid hybrid species Senecio squalidus, we review evidence showing: (1) that new fertile homoploid hybrid species can originate very quickly, although a longer period is likely to be required before the species becomes fully stabilized both genomically and phenotypically; (2) ecological divergence of the hybrid species from its parents is key to successful establishment, and that this can occur even in the absence of post­zygotic isolation caused by chromosomal and/or genetic sterility barriers; (3) transgressive changes in phenotypic traits and gene expression are of great importance in adapting homoploid hybrid species to habitats that are ecologically and spatially divergent from those of the parents; (4) adaptive differences distinguishing a homoploid hybrid species from its parental species are likely to be maintained in the face of parental gene flow, and evolve in concert across populations representing multiple origins of the species; (5) in the absence of parental gene flow, i.e., under conditions of geographical isolation, rapid genetic divergence of the hybrid species is likely to be enhanced due to the combined effects of founder events, genetic drift and selection.

Summary• Hybrid zone theory provides a powerful theoretical framework for measuring and testing gene flow and selection. The Senecio aethnensis and Senecio chrysanthemifolius hybrid zone on Mount Etna, Sicily, was investigated to identify phenotypic traits under divergent selection and to assess the contributions of intrinsic and extrinsic selection against hybrids to hybrid zone maintenance.• Senecio samples from 14 sites across Mount Etna were analyzed for 24 quantitative traits classified into four groups (QTGs), six allozymes and seven simple sequence repeat (SSR) loci to describe patterns of variation throughout the hybrid zone.• Narrower cline widths or shifts in cline centre position were observed for three QTGs relative to the molecular clines, indicating that these traits are likely to be under extrinsic environmental selection. Altitude was key to describing species distributions, but dispersal and intrinsic selection against hybrids explained patterns at smaller spatial scales. The hybrid zone was characterized by strong selection against hybrids, high dispersal rates, recent species contact and few loci differentiating QTGs based on indirect measures.• These results support the hypothesis that extrinsic and intrinsic selection against hybrids maintains the hybrid zone and species distinctiveness despite gene flow between the two Senecio species on Mount Etna.

Twenty-six individuals of the sporophytic self-incompatible (SSI) weed, Senecio squalidus were crossed in a full diallel to determine the number and frequency of S alleles in an Oxford population. Incompatibility phenotypes were determined by fruit-set results and the mating patterns observed fitted a SSI model that allowed us to identify six S alleles. Standard population S allele number estimators were modified to deal with S allele data from a species with SSI. These modified estimators predicted a total number of approximately six S alleles for the entire Oxford population of S. squalidus. This estimate of S allele number is low compared

Interspecific hybridization is an important mechanism of speciation in higher plants. In flowering plants, hybrid speciation is usually associated with polyploidy (allopolyploidy), but hybrid speciation without genome duplication (homoploid hybrid speciation) is also possible, although it is more difficult to detect. The combination of divergent genomes within a hybrid can result in profound changes to both genome and transcriptome. Recent transcriptomic studies of wild and resynthesized homoploid and allopolyploid hybrids have revealed widespread changes to gene expression in hybrids relative to expression levels in their parents. Many of these changes to gene expression are 'nonadditive', i.e. not simply the sum of the combined expression levels of parental genes. Some gene expression changes are far outside the range of gene expression in either parent, and can therefore be viewed as 'transgressive'. Such profound changes to gene expression may enable new hybrids to survive in novel habitats not accessible to their parent species. Here, we give a brief overview of hybrid speciation in plants, with an emphasis on genomic change, before focusing discussion on findings from recent transcriptomic studies. We then discuss our current work on gene expression change associated with hybrid speciation in the genus Senecio (ragworts and groundsels) focusing on the findings from a reanalysis of gene expression data obtained from recent microarray studies of wild and resynthesized allopolyploid Senecio cambrensis. These data, showing extensive non-additive and transgressive gene expression changes in Senecio hybrids, are discussed in the light of findings from other model systems, and in the context of the potential importance of gene expression change to hybrid speciation in plants.

Hybridization is an important cause of abrupt speciation. Hybrid speciation without a change in ploidy (homoploid hybrid speciation) is well-established in plants but has also been reported in animals and fungi. A notable example of recent homoploid hybrid speciation is Senecio squalidus (Oxford ragwort), which originated in the UK in the 18th Century following introduction of hybrid material from a hybrid zone between S. chrysanthemifolius and S. aethnensis on Mount Etna, Sicily. To investigate genetic divergence between these taxa, we used complementary DNA microarrays to compare patterns of floral gene expression. These analyses revealed major differences in gene expression between the parent species and wild and resynthesized S. squalidus. Comparisons of gene expression between S. aethnensis, S. chrysanthemifolius and natural S. squalidus identified genes potentially involved in local environmental adaptation. The analysis also revealed non-additive patterns of gene expression in the hybrid relative to its progenitors. These expression changes were more dramatic and widespread in resynthesized hybrids than in natural S. squalidus, suggesting that a unique expression pattern may have been fixed during the allopatric divergence of British S. squalidus. We speculate that hybridization-induced gene-expression change may provide an immediate source of novel phenotypic variation upon which selection can act to facilitate homoploid hybrid speciation in plants.