Cinnyris, Cuvier, 1816
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https://doi.org/10.1093/zoolinnean/zlac081 |
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https://treatment.plazi.org/id/03A187E4-FF9C-FFB3-8609-D894D8C8FAA8 |
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Plazi (2025-02-12 10:01:05, last updated 2025-02-12 11:50:01) |
scientific name |
Cinnyris |
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CINNYRIS View in CoL TAXONOMY
Our results indicate that the olive-backed sunbird represents a superspecies and should be split into at least four species (Supporting Information, Table S10). We have found support for the three-way split suggested by Eaton et al. (2021) while also providing the first genetic, acoustic and morphological evidence that the ‘Wakatobi sunbird’ warrants recognition as a full species. The Wakatobi population exhibits a strikingly non-linear arrangement of population structure, with a range enveloped within that of the more widespread species, and had previously been suggested as a ‘limbo split’ (Rheindt, 2021) based on plumage differences alone ( Eaton et al., 2021). Our study has supported these differences with matching patterns in mtDNA and integrative species delimitation or ‘Tobias scoring’ ( Tobias et al., 2010). Due to the lower effective population size of mtDNA, along with other factors, differences in mtDNA should be integrated with other forms of evidence in this way ( Rubinoff & Holland, 2005). In the light of this new integrative evidence, we recommend that the ‘Wakatobi sunbird Cinnyris infrenatus ’, originally named by Hartert (1903), be reinstated as a separate species. In addition to its genetic divergence ( Fig. 3), the ‘Wakatobi sunbird’ has shorter wings, a shorter bill and longer tarsi than the ‘Sahul sunbird’ (Supporting Information, Fig. S9), as well as exhibiting slower and higher pitched calls over a smaller bandwidth (Supporting Information, Fig. S11). This study is one of several to have remarked upon the distinctness of the Wakatobi avifauna ( Kelly et al., 2014; O’Connell et al., 2019a, c), and so we reiterate the recommendation of O’Connell et al. (2020) that the Wakatobi Islands should be protected as an Endemic Bird Area ( Stattersfield et al., 1998).
In addition to the distinctive nature of the Wakatobi lineage, our work supports the splits suggested by Eaton et al. (2021) and one possible additional split in the Philippines ( Fig. 5). Under the Eaton et al. (2021) treatment, populations from Sulawesi to the Sahul Shelf and the Solomon Islands were recognized as a species-level taxon, the ‘Sahul sunbird Cinnyris clementiae ’, the Sunda Shelf populations become ‘ornate sunbird Cinnyris ornatus ’ and the Philippine birds retain the Cinnyris jugularis name and take ‘garden sunbird’ as a common name. This is supported by deep genetic divergences (all greater than 5%) between these three putative species, with the Sahul Shelf represented by our new Sulawesi, Australian and PNG sequences along with Solomon Islands birds from Smith & Filardi (2007), the Sunda Shelf by a sequence from Borneo ( Boyce et al., 2019) and the Philippines by a number of previously published partial sequences (Supporting Information, Table S3). Although this split has been suggested previously based on limited sampling and incomplete sequences, our more comprehensive sampling of full sequences, taken from both ends of the new ‘Sahul sunbird’ species range, offers stronger support for the division. Our study has also suggested another potential split in this species complex ( Fig. 5), outside the geographic range covered in detail by Eaton et al. (2021). ABGD considered the aurora sequences from Busuanga in the western Philippines to represent a distinct species, with a mean genetic distance of 4.5%, from the greater Philippine archipelago (subspecies obscurior and jugularis ). Ornithologists ( Rand, 1951; Billerman et al., 2022) have grouped the aurora subspecies separately from these other Philippine subspecies due to its orange breast plumage. The western chain of islands on which the aurora subspecies occurs is geologically and biogeographically distinct from the greater Philippine archipelago ( Diamond & Gilpin, 1983). The aurora subspecies displayed a similar level of genetic divergence to that of the more thoroughly sampled ‘Wakatobi sunbird’, but was represented in our analysis by two partial ND2 sequences from Campbell (2013), and so we recommend further sampling of this population.
The lack of divergence between the Menui population and the wider south-east Sulawesi population in the ‘Sahul sunbird’ confirms that the Menui population belongs to the plateni subspecies. On the Sahul Shelf itself, our ‘Sahul sunbirds’ exhibit a uniform population across PNG and Australia. This is in keeping with the current assignment of these populations to one subspecies, Cinnyris jugularis frenatus .
Billerman SM, Keeney BK, Rodewald PG, Schulenberg TS. 2022. Birds of the world. Ithaca: Cornell Laboratory of Ornithology.
Boyce AJ, Shakya S, Sheldon FH, Moyle RG, Martin TE. 2019. Biotic interactions are the dominant drivers of phylogenetic and functional structure in bird communities along a tropical elevational gradient. The Auk 136: ukz 054.
Campbell KK. 2013. Evolution in a tropical archipelago: comparisons within and among 50 species of Philippine birds. Unpublished Master of Science Thesis, University of Alaska Fairbanks.
Diamond JM, Gilpin ME. 1983. Biogeographic umbilici and the origin of the Philippine avifauna. Oikos 41: 307-321.
Eaton JA, van Balen B, Brickle NW, Rheindt FE. 2021. Birds of the Indonesian Archipelago: Greater Sundas and Wallacea, 2 nd ed. Barcelona: Lynx Edicions.
Hartert E. 1903. On the birds collected on the Tukang-Besi islands and Buton, south-east of Celebes, by Mr Heinrich Kuhn. Novitates Zoologicae 10: 18-38.
Kelly SBA, Kelly DJ, Cooper N, Bahrun A, Analuddin K, Marples NM. 2014. Molecular and phenotypic data support the recognition of the Wakatobi flowerpecker (Dicaeum kuehni) from the unique and understudied Sulawesi region. PLoS One 9: e 98694.
O'Connell DP, Kelly DJ, Kelly SBA, Sealy S, Karya A, Analuddin K, Marples NM. 2019 a. Increased sexual dimorphism in dense populations of olive-backed sunbirds on small islands: morphological niche contraction in females but not males. Emu - Austral Ornithology 119: 296-307.
O'Connell DP, Kelly DJ, Kelly SBA, Analuddin K, Karya A, Marples NM, Rheindt FE, Martin TE. 2020. An assessment of the avifauna of the Wakatobi Islands, south-east Sulawesi, Indonesia: species recorded and taxonomic considerations. Raffles Bulletin of Zoology 68: 574-587.
Rand AL. 1951. Review of the subspecies of the sunbird Nectarinia jugularis. Fieldiana Zoology 31: 597-607.
Rubinoff D, Holland BS. 2005. Between two extremes: mitochondrial DNA is neither the panacea nor the nemesis of phylogenetic and taxonomic inference. Systematic Biology 54: 952-961.
Smith CE, Filardi CE. 2007. Patterns of molecular and morphological variation in some Solomon Island land birds. The Auk 124: 479-493.
Stattersfield AJ, Crosby MJ, Long AJ, Wege DC. 1998. Endemic bird areas of the world: priorities for biodiversity conservation. Cambridge: BirdLife International.
Tobias JA, Seddon N, Spottiswoode CN, Pilgrim JD, Fishpool LDC, Collar NJ. 2010. Quantitative criteria for species delimitation. Ibis 152: 724-746.
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