Subgenus Phoniomyia Theobald, 1903
Wyeomyia longirostris Theobald, 1901.
Subfamily Culicinae, genus Wyeomyia. Subgenus Phoniomyia includes 22 species. Subgenus abbreviation – Pho.
ADULTS ‒ Proboscis unusually long and slender, much longer than forefemur, curved downward; mesopostnotal setae present; paratergite without scales; lower mesokatepisternal setae not extending above dorsal margin of mesomeron; upper calypter of wing without marginal setae. MALE GENITALIA ‒ Tergum IX lobes weakly to strongly produced, setae short and stout or longer and narrower and often with apices bent laterad; gonocoxite rather long and relatively slender, tergal triad and basal mesal lobe absent; gonostylus either usually short and setose or divided proximally into 2 long arms, longer ventral arm with an elongate knife-like arm along one side; aedeagus elongate, apical tergal arms not fused to form an apical tergal bridge; proctiger with apical teeth, cercal setae present. LARVAE ‒ Setae 4‒6-C usually multi-branched (may be single or double in Wy. theobaldi), 4-C not inserted close to median labral plate, on level with antennal prominence, 6-C inserted anterior to seta 7-C, 5-C usually inserted more or less on level with seta 7-C (distinctly anterior to 7-C in Wy. palmata); seta 1-A single or branched, inserted about 0.75 from base of antenna; maxilla longer than wide, with very small apical tooth, seta 3-Mx borne in lateral cup-like notch (as in species of Hystatomyia), seta 4-Mx single, stout, brush-tipped, as long as or longer than maxillary brush, seta 6-Mx single, arising from distinct hypostomal sclerite or sclerite unapparent with seta 6-Mx apparently arising from membrane; seta 15-C inserted posterior to seta 12-C at level of mid-length of labiogula; seta 1-P multi-branched, as long as or slightly shorter than seta 2-P; seta 4-P short, multi-branched; seta 11-P,M,T normal, not spine-like; seta 4-T relatively large, about as long as seta 1-M; seta 13-T multi-branched, about 0.5 length of thorax; comb plate absent, comb scales generally numerous, in patch; siphon long and tapered, with single or 2 close-set posterior rows of pecten spines, seta 1-S branched, inserted about 0.25 from base of siphon, setae la,2a-S long and numerous; saddle without spicules on posterior margin; seta 1-X with 1‒3 branches, usually double; seta 4-X multi-branched, very short, <0.25 length of seta 1-X. PUPAE ‒ Cephalothorax and abdomen often with variable pattern of pigmentation; trumpet slender and more or less cylindrical; seta 1-I strongly developed, dendritic; 2-II‒VII inserted near posterior margin of terga, 2-II inserted between setae 1,3-II, seta 2-III‒VII inserted mesal to seta 1; seta 3-II inserted lateral to seta 1, 3-IV‒VI inserted anterolateral to seta 1; seta 6-II single, long, reaching well beyond posterior margin of tergum III, seta 6-VII inserted on tergum posterior to seta 9-VII; paddle length variable, as long as or distinctly longer than tergum VIII, generally ovoid, apex rounded or slightly narrowed, with or without short apical spicules. See genus Wyeomyia.
Phoniomyia was sister to Hystatomyia (as Dendromyia ‘species A group’) in the cladistic analysis of combined larval, pupal and adult morphological data in the phylogenetic study of Sabethini conducted by Judd (1996). Later analyses of clades most closely associated with Phoniomyia and Hystatomyia (Judd, 1998) generated two topologies, one with the sister relationship of Phoniomyia + Hystatomyia and another with Phoniomyia + Nunezia, from the combined larval, pupal and adult data. The former relationship was retained when the larval data were analysed alone, and the latter was recovered when only adult characters were analysed. In the absence of species of Hystatomyia, Phoniomyia was recovered, with very weak support, as a lineage outside Wyeomyia in the phylogenetic study of Motta et al. (2007).
The immature stages of Phoniomyia normally inhabit the axils of arboreal and terrestrial bromeliads, however larvae of Wy. pilicauda have been found in the leaf axils of a terrestrial aroid (Xanthosoma) (Heinemann & Belkin, 1979) and those of Wy. trinidadensis have been taken from the leaf axils of Dracaena in a domestic area (Heinemann et al., 1980). The adults occur in damp forests and plantations in the immediate vicinity of larval habitats. They are principally active during the daylight hours, but some species remain active during diurnal periods and Wy. lassalli is active during the night (Guimarães et al., 2000). Females are known to bite humans (see e.g. Heinemann et al., 1980; Paterno & Marcondes, 2004) as well as other animals. The adults of various species have been collected in bird-baited traps at all elevations in forest canopy in Brazil. Species of Phoniomyia are of no medical or economic importance to humans.
All species of subgenus Phoniomyia, except Wy. trinidadensis, are known to occur in Brazil ‒ Wy. trinidadensis is recorded from Trinidad and Tobago, and Venezuela. Only six of the species recorded from Brazil reportedly occur in other countries, including Argentina (Wy. muehlensi, Wy. quasilongirostris, Wy. tripartita), Bolivia (Wy. muehlensi), French Guiana (Wy. splendida), Guyana (Wy. splendida), Paraguay (Wy. fuscipes), Suriname (Wy. splendida), and Trinidad and Tobago (Wy. lassalli, Wy. splendida).
Correa & Ramalho, 1956 (as genus, keys, taxonomy, morphology); Judd, 1996 (morphology, phylogenetic relationships); Judd, 1998 (subgeneric status, phylogenetic relationships); Motta et al., 2007 (morphology, phylogenetic relationships); Porter, 2014 (comparative morphology).
antunesi Lane & Guimarães, 1937
bonnei (Lane & Cerqueira, 1942)
davisi (Lane & Cerqueira, 1942)
deanei (Lourenço de Oliveira, 1983)
diabolica (Lane & Forattini, 1952)
edwardsi (Lane & Cerqueira, 1942)
flabellata (Lane & Cerqueira, 1942)
fuscipes Edwards, 1922
galvaoi (Correa & Ramalho, 1956)
incaudata Root, 1928 (in Dyar, 1928)
lassalli (Bonne-Wepster & Bonne, 1921)
longirostris Theobald, 1901
lopesi (Correa & Ramalho, 1956)
muehlensi Petrocchi, 1927 (in Shannon & del Ponte, 1927)
pallidoventer (Theobald, 1907)
palmata (Lane & Cerqueira, 1942)
pilicauda Root, 1928 (in Dyar, 1928)
quasilongirostris (Theobald, 1907)
splendida Bonne-Wepster & Bonne, 1919
theobaldi (Lane & Cerqueira, 1942)
trinidadensis Theobald, 1901
tripartita (Bonne-Wepster & Bonne, 1921)