Subgenus Wyeomyia Theobald, 1901
Wyeomyia grayii Theobald, 1901.
Subfamily Culicinae, genus Wyeomyia. Subgenus Wyeomyia includes 35 species. Subgenus abbreviation – Wyo.
Subgenus Wyeomyia is difficult to characterise because most species are poorly known and probably do not comprise a monophyletic group (see below); consequently, some of the characteristics listed here are unlikely to be shared by all species currently included in the subgenus. ADULTS ‒ Proboscis short, shorter than forefemur, slightly enlarged distally; mesopostnotal setae present; paratergite with or 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 developed, each bearing 2 or more unmodified setae; gonocoxite elongate, lateral and ventral surfaces with numerous scales, basal mesal lobe and tergal triad present; gonostylus with distinct stem and large head comprised of variously developed lobes, large median lobe M always present, lobe A indistinct to well developed, lobe E present, absent or not differentiated from lobes A or M, lobes B and C present or absent; aedeagus longer than wide, apical tergal arms not separate, not forming an apical tergal bridge; proctiger normal, paraproct with ill-defined apical teeth, cercal setae present, sometimes numerous and longer than usual. LARVAE ‒ Setae 4‒6-C single or branched, 5-C inserted posterior, more or less on level or anterior to seta 7-C; seta 1-A single or branched, inserted on distal 0.25 of antenna, sometimes very near apex; maxilla nearly as broad as long, without prominent apical tooth, seta 3-Mx not borne in lateral cup-like notch, seta 4-Mx single, simple, hypostomal sclerite fused (partially?) with maxillary body; seta 14-C moderately well developed, single or with relatively few branches, generally 2‒4 times as long as seta 15-C (14-C very long with numerous branches in Wy. nigritubus), inserted more or less on level with or slightly anterior to seta 15-C at approximately mid-length of labiogula; seta 1-P usually multi-branched, inserted mesad to posteromesad of setae 2,3-C approximately midway between these setae and midline of thorax; seta 4-P multi-branched, shorter to longer than seta 3-C; seta 4-T relatively large, multi-branched (except in Wy. nigritubus); seta 11-P,M,T branched (single in Wy. nigritubus), branches flexible; seta 13-T multi-branched, long, about 0.75 to full length of thorax; insertions, positional relationships and development of setae 1,2,13-I‒VII varied, seta 1 generally inserted more posterolaterad than usual, seta 2 generally inserted far anterior to anteromesad of seta 1; seta 9-I‒VI with 2 or more branches; seta 13-I inserted far anterior to other ventral setae but seta 9-I sometimes inserted more or less at same level, 13-II‒VI inserted posterior to other setae (except in Wy. nigritubus); comb plate absent, comb a single long row of close-set spine-like scales; siphon without pecten, seta 1-S inserted on proximal 0.25 of siphon, setae la,2a-S each a more or less straight row of many to numerous elements (few elements in Wy. nigritubus); saddle with or without posterolateral spicules; seta 4-X multi-branched, usually about 0.5 length of seta 1-X (shorter in Wy. nigritubus). PUPAE ‒ Cephalothorax and abdomen, especially anterior terga, with pattern of pigmentation (except Wy. nigritubus); trumpet short, laterally expanded; seta 1-I strongly developed, dendritic; seta 2-II‒VII inserted anterior, anteromesal or mesal to seta 1; seta 3-V,VI inserted anterior to anteromesad of seta 1 (anterolateral in Wy. nigritubus); seta 6-II single, as long as to slightly longer than tergum III, 6-VII inserted on tergum posteromesal to seta 9-VII (inserted on sternum in Wy. corona); paddle variable, longer than wide, length usually >1.5x width, usually distinctly longer than tergum VIII, outer part distinctly wider than inner part, narrowed apically, apex and at least distal margins minutely spiculate (margins fringed with long spicules in Wy. mitchellii). See genus Wyeomyia.
The phylogenetic relationships of subgenus Wyeomyia are unknown. Belkin et al. (1970) recognised “four more or less distinct phyletic lines” among species of the subgenus in Jamaica and noted that Wy. nigritubus “is so distinct from the other species… that it should eventually be placed in a different subgenus”. Judd (1996) included only Wy. arthrostigma and Wy. grayii in her morphology-based phylogenetic analyses of Sabethini, and Motta et al. (2007) included only Wy. arthrostigma and Wy. medioalbipes in their phylogenetic analyses of genus Wyeomyia, also based on morphological data. The results of both studies suggest that the subgenus is not a monophyletic taxon. The two species included in the latter study shared a paraphyletic relationship with a clade comprised of species of Miamyia.
The immature stages of species of subgenus Wyeomyia occupy a range of phytotelm habitats, but are found primarily in terrestrial and arboreal bromeliads. Larvae of several species also have been found occasionally in leaf axils of aroids, flower bracts of Heliconia, bamboo sections and stumps, fallen cocoa pods, coconut shells and tree holes. Larvae of Wy. arthrostigma and Wy. nigritubus occur primarily in bamboo habitats (Belkin et al., 1970; Heinemann & Belkin, 1977, 1978a, 1978b, 1978c, 1979; Heinemann et al., 1980). The immature stages of Wy. smithii develop in the leaves of the pitcher plant Sarracenia purpurea (Carpenter & LaCasse, 1955). Females of several species are often encountered in forest during the daytime and are known to land on and bite humans, e.g. Wy. hirsuta, Wy. mitchellii and Wy. vanduzeei (Belkin et al., 1970; Carpenter & LaCasse, 1955).
Species of subgenus Wyeomyia occur mainly in areas from Brazil and Ecuador northward through Central America and the Caribbean Islands. One species (Wy. hemisagnosta) is recorded from as far south as Bolivia; two species, Wy. vanduzeei and Wy. mitchellii, are recorded from various Caribbean Islands and Florida and Georgia in the southeastern United States. Wyeomyia smithii is the only temperate species of the genus, with a distribution in the northeastern United States from Illinois eastward to Delaware and southern Canada from Saskatchewan eastward to Newfoundland.
Belkin et al., 1970 (Jamaica, 8 formally named and 2 unnamed species, keys, morphology, descriptions, bionomics, distributions); Judd, 1996 (morphology, phylogenetic relationships); Motta et al., 2007 (morphology, phylogenetic relationships).
abebela Dyar & Knab, 1908
ablechra Dyar & Knab, 1908
adelpha Dyar & Knab, 1906
arthrostigma (Lutz, 1905)
atrata Belkin, Heinemann & Page, 1970
bahama Dyar & Knab, 1906
caracula Dyar & Núñez Tovar, 1928
celaenocephala Dyar & Knab, 1906
charmion Dyar, 1928
corona Belkin, Heinemann & Page, 1970
downsi Lane, 1945
florestan Dyar, 1925
gaudians Dyar & Núñez Tovar, 1927
gausapata Dyar & Núñez Tovar, 1927
grayii Theobald, 1901
guatemala Dyar & Knab, 1906
hemisagnosta Dyar & Knab, 1906
hirsuta (Hill & Hill, 1946)
juxtahirsuta Belkin, Heinemann & Page, 1970
labesba Howard, Dyar & Knab, 1913, 1915
luna Belkin, Heinemann & Page, 1970
medioalbipes Lutz, 1904 (in Bourroul, 1904)
melanopus Dyar, 1919
mitchellii (Theobald, 1905)
nigritubus Galindo, Carpenter & Trapido, 1951
pertinans (Williston, 1896)
pseudorobusta Pajot & Fauran, 1975
robusta Senevet & Abonnenc, 1939
scotinomus (Dyar & Knab, 1907)
simmsi (Dyar & Knab, 1908)
smithii (Coquillett, 1901)
sororcula Dyar & Knab, 1906
stellata Belkin, Heinemann & Page, 1970
stonei Vargas & Martínez Palacios, 1953
vanduzeei Dyar & Knab, 1906