Most diploid species arise from single-species ancestors. Hybrid origins of new species are uncommon (except among polyploids) and are documented infrequently in animals. Examples of natural hybridization leading to speciation in mammals are exceedingly rare. Here, we show a Caribbean species of bat (Artibeus schwartzi) has a nuclear genome derived from two nonsister but congeneric species (A. jamaicensis and A. planirostris) and a mitochondrial genome that is from a third extinct or uncharacterized congener. Artibeus schwartzi is self-sustaining, morphologically distinct, and exists in near geographic isolation of its known parent species. Island effects (i.e., area, reduced habitat variability, and geographic isolation) likely have restricted gene flow from parental species into the Caribbean populations of this hybrid lineage, thus contributing to local adaptation and isolation of this newly produced taxon. We hypothesize differential rates of the development of reproductive isolation within the genus and estimate that 2.5 million years was an insufficient amount of time for the development of postzygotic isolation among the three species that hybridized to produce A. schwartzi. Reticulated evolution thus has resulted in a genomic combination from three evolutionary lineages and a transgressive phenotype that is distinct from all other known species of Artibeus. The data herein further demonstrate the phenomenon of speciation by hybridization in mammals is possible in nature.Artibeus | Chiroptera | hybrid speciation | reticulate evolution | transgressive segregation D espite empirical studies documenting the establishment of animal hybrid lineages (1-8), the evolutionary importance of speciation by natural hybridization in animals is unknown and often is considered minor because the offspring of such crosses typically are less fit than either parental species (9, 10). Nearly all reported cases of homoploid speciation events (hybrid speciation without change in chromosome number) (11) in animals are among species of insects or fish (12), and there are only a handful of suspected cases in mammals (13-17). Thus hybrid speciation appears to be especially rare in mammals, a consequence of either unfavorable conditions for hybrid speciation to occur (i.e., ecological, physiological, hybrid zone structure) or a lack of empirically based research (18,19). Here, we describe a zone of admixture on a series of Caribbean islands within which three species of Neotropical bats have hybridized resulting in a novel lineage with species-level distinction. Our genetic and morphometric analyses have identified a unique hybrid zone among species of fruit-eating bats, leading us to the hypothesis that natural hybridization has generated a distinct lineage that exists in these insular populations. Our data also indicate that this phenotypic and genotypic combination is geographically isolated from extant parental species on the southern Lesser Antillean island of Saint Vincent.Two species of fruit-eating bats, Artibeus jamaicensis...