The Elegant Pitta (Pitta elegans) complex displays a remarkable diversity of morphological and bioacoustic traits across five taxa currently recognized as subspecies. They differ in plumage characteristics (such as red versus black belly patches; supercilium color and extent; and white versus black throats), in lifestyle (resident versus migratory) and in vocalizations. We investigated the morphological, bioacoustic and ecological differences across all taxa after recent studies demostrated the importance of these traits in recognizing biological species limits across pittas.

Morphometric analysis was carried out by measuring tarsus, wing, tail and bill lengths of 15 specimens at the Natural History Museum, UK, and plumages were inspected across 106 unique individuals from four different repositories. Bioacoustic analysis was based on 134 range-wide sound recordings. Two types of calls, territorial calls and alarm calls, were analyzed using different sets of parameters. Principal component analysis and the Isler Criterion were applied to the measurements. Playback trials were conducted to explore the levels of response of each taxon to the call types of the other taxa.

The territorial call of concinna exhibits a distinct two-element motif, while elegans, maria and virginalis utter a three-element motif in which the first two elements are given in quick succession. On the other hand, vigorsii, produces both two-element and three-element motifs with longer breaks in between elements. As further corroborated by the playback trials, the three taxa elegans, virginalis and maria form a tight vocal cluster, whereas each concinna and vigorsii are distinct. The alarm call turned out to be less diagnostic even though most taxa did roughly separate into different vocal clusters. Morphometric analysis failed to produce strong differences, but plumage distinctions among multiple taxa are pronounced.

We suggest splitting the Elegant Pitta into three biological species based on bioacoustic and—less so—plumage evidence: (1) Temminck's Elegant Pitta P. elegans (including subspecies elegans, virginalis and maria), (2) Wallace's Elegant Pitta P. concinna (monotypic), and (3) Banda Elegant Pitta P. vigorsii (monotypic).

The taxonomy of the Collared Owlet (Glaucidium brodiei) species complex is confused owing to great individual variation in plumage colouration seemingly unrelated to their distribution. Although generally recognised as a single species, vocal differences among the subspecies have been noted by field recordists. However, there is no study assessing the vocal differences among these four subspecies.

We obtained 76 sound recordings of the G. brodiei species complex comprising all four subspecies. We conducted bioacoustic examinations using principal component analysis and the Isler criterion to quantitatively test species boundaries within the G. brodiei complex. In addition, we compared plumage colouration among 13 specimens of the G. brodiei complex deposited at the Natural History Museum at Tring, UK and the Lee Kong Chian Natural History Museum, Singapore to ascertain the presence of plumage differences across taxa.

We found the Bornean and Sumatran populations vocally similar to each other, but distinctly different from the mainland and Taiwan populations. The vocal pattern seems to corroborate plumage distinctions in the colouration of neck collars: the Bornean and Sumatran taxa share a white neck collar, whereas the continental and Taiwan taxa share a rufous neck collar.

We propose the taxonomic elevation of the Sumatran and Bornean populations to species level as Sunda Owlet G. sylvaticum, with one subspecies on Sumatra (G. s. sylvaticum) and Borneo (G. s. borneense) each. Our study corroborates the importance of bioacoustics in ascertaining species boundaries in non-passerines, and emphasises the significance of incorporating multiple species delimitation approaches when making taxonomic decisions.

The White-faced Cuckoo-dove (Turacoena manadensis) is a poorly-known Wallacean endemic with a limited distribution on Sulawesi and its satellites, including the Togian, Banggai and Sula archipelagoes. In 1900, populations from the Sula archipelago were awarded subspecies status T. manadensis sulaensis based on smaller size and minor differences in plumage; however, this distinction has not been corroborated subsequently, and T. manadensis is considered by most modern sources to be monotypic across its range.

We conducted vocal analysis of the cuckoo-doves' main song using recordings collected from across the taxon's natural range. Descriptive information on the songs was obtained from the recordings using bioacoustic analysis software, after which several statistical methods were used to investigate differences in vocalizations among populations.

We report deep bioacoustic divergences in vocal trait pattern from across the cuckoo-doves' range, with birds from Peleng and Taliabu in the east having a different vocal trait pattern from birds from Sulawesi, Buton, and Togian in the west. These patterns agree with changes in landmass that accompanied the sea level fluctuations caused by Pleistocene glacial cycles, and indicate that eastern and western cuckoo-dove populations are at the level of different biological species.

We propose that the eastern taxon be elevated to species level as T. sulaensis. Given the rampant degree of habitat destruction in its limited range, this taxonomic change will have important implications on the conservation status of T. sulaensis.

The Brown Hawk Owl complex is said to consist of three species, the Brown Boobook (Ninox scutulata), the Chocolate Boobook (Ninox randi) and the Northern Boobook (Ninox japonica), which includes the nominate migratory lineage Ninox japonica japonica and a mitochondrially distinct lineage of taxonomically uncertain status that has been recorded year-round at least in Taiwan. Overlap in ranges during migration and morphological similarity have led to difficulties in distinguishing the Brown Boobook from the Northern Boobook.

PCR of cytochrome-b and Sanger sequencing of Ninox samples from Singapore and Brunei were used to determine sample identity.

Two out of four Singaporean samples and the Brunei sample were identified as Northern Boobooks. This is the first official record of this species in Singapore and represents a considerable range extension for the species. Further, the samples belong to the mitochondrially distinct lineage previously characterized in resident Taiwanese populations rather than to the well-known nominate migratory lineage.

Our data show that the mitochondrial signature previously documented in resident Taiwanese populations of the Northern Boobook extends to migratory populations. This cryptic lineage may be more widespread in its breeding quarters, extending to the Chinese and Russian mainland, in which case the name florensis would apply to it. Further genetic and bioacoustic investigation is required to resolve the taxonomic status of this lineage.