Subgenus Eumelanomyia Theobald, 1909
Culex inconspicuosus (Theobald, 1908), original combination: Eumelanomyia inconspicuosa.
Subfamily Culicinae, genus Culex. Subgenus Eumelanomyia includes 79 species. See Culex classification, Subgenus Eumelanomyia). Subgenus abbreviation – Eum.
ADULTS – Small to medium-sized dark unornamented mosquitoes; vertex with narrow to broad scales; antenna as long or longer than proboscis in females, shorter than or as long as proboscis in males; maxillary palpus and proboscis dark-scaled; palpus of females with 3 or 4 palpomeres, palpomere 4 vestigial or absent; palpus of males with 3–5 palpomeres, distinctly shorter than proboscis; proboscis as long or slightly longer than forefemur; proboscis of males with or without false joint; scutal scales narrow and predominantly dark; acrostichal setae usually present anteriorly, sometimes absent or only a few present; pleural scales absent or very few present on mesokatepisternum; lower mesepimeral seta present or absent; wing dark-scaled, cell R2 distinctly longer than vein R2+3; tibiae and tarsi dark-scaled; ungues of all legs small, equal and simple in females, fore- and midungues enlarged in males, one larger than the other, each with a small denticle; pulvilli poorly or well developed; abdominal terga usually entirely dark-scaled, sometimes with pale basal bands or basolateral spots. MALE GENITALIA – Tergum IX lobes usually small, sometimes large and prominent, setose; gonocoxite without scales; subapical lobe usually small, not clearly divided, proximal division with 3 rod-like setae; distal division with or without 1 strong basal seta and 1 foliform seta, always with a variable number of hair-like or blade-like setae mesally; gonostylus simple or strongly modified; gonostylar claw well developed, length and thickness varied, usually subapical, sometimes apical; phallosome oval to nearly spherical in shape, tergal bridge median or submedian in position, lateral plates usually with denticles on upper tergal surface; paraproct with crown of fine spine-like spicules (absent in Cx. manusensis), some coarse ones sometimes present; proctiger with crown of varied spicules, basal sternal process absent; cercal setae present. LARVAE – Head broader than long; antenna as long as head, spiculate, seta 1-A well developed, inserted distal to mid-length, setae 2,3-A at or removed from apex; seta 1-C stout, spine-like; setae 5,6-C varied in length and position; seta 3-P much shorter than setae 1,2-P; seta 4-P varied in length from shorter than seta 3-P to as long as setae 1,2-P; seta 7-I strong, similar to seta 6-I, seta 7-II small, similar to 7-III–VI; comb comprised of numerous fringed scales in patch; siphon slender, moderately long to very long, pecten restricted to basal area, spines varied in shape; 4–6 posterolateral pairs of seta 1-S present; saddle complete, without conspicuous spicules; setae 2,3-X long, seta 2-X single or with short accessory branches, seta 3-X single; ventral brush (seta 4-X) usually with 4.5–8 pairs of seta on grid. PUPAE – Trumpet usually cylindrical, pinna with or without slit extending into meatus; seta 6-I,II well developed, longer than seta 7; seta 2-II inserted laterad of setae 1,3-I, seta 2-III–VI inserted mesad of seta 1, seta 2-VII insserted mesad or laterad of seta 1; seta 5-IV–VI well developed, larger than 5-III,VII; seta 9-VIII shorter than tergum, inserted anteromesal to caudolateral angle of sternum; paddle broad and oval, margins smooth; seta 1-Pa present or absent; seta 2-Pa present. See genus Culex.
Sirivanakarn (1971, 1972) hypothesised a close relationship between Eumelanomyia, Maillotia and Neoculex based on morphological similarities of the adults and male genitalia, and suggested that Eumelanomyia is an ancient derivative of the Maillotia lineage. He also suggested that the Eumelanomyia lineage probably gave rise to subgenus Lophoceraomyia. Sirivanakarn (1972) also noted similarities between the adults of Eumelanomyia and Culiciomyia. The results of the study by St John (2007) indicate a closer relationship with Culiciomyia and Lophoceraomyia than with Maillotia and Neoculex. A limited molecular study by Juthayothin (2004) using the COI gene of mitochondrial DNA showed poor resolution among subgenera Culiciomyia, Eumelanomyia and Culex. Based on this sole molecular marker, Eumelanomyia seemed to be the most primitive of the three subgenera; however, substantial homoplasy was detected in the data set making this conclusion unreliable. The results of the phylogenetic study of Harbach et al. (2012) based on morphological data indicate that Eumelanomyia is not a monophyletic group.
Eumelanomyia species are common in tropical forests in inland hilly and mountainous terrain. The immature stages are found in various ground pools, rock pools, rock holes, tree holes, bamboo and artificial containers, generally containing little organic matter. The adults of most species have been collected resting on vegetation in the vicinity of streams and swamps. Nothing is known about the feeding habits of females.
Eumelanomyia have not been incriminated as vectors of human disease agents, but three different viruses have been isolated from a single species in South Africa.
Afrotropical and Oriental Regions, with extensions into the Papuan Subregion and South Pacific of the Australasian Region and the Manchurian Subregion of the Palaearctic Region.
Sirivanakarn, 1971 (taxonomy, keys and descriptions of species groups and subgroups), 1972 (revision, subgenus and species descriptions, keys for groups and species, bionomics, distributions); Tanaka et al., 1979 (Japan, subgenuks and species descriptions, keys, bionomics, distributions); Lee et al., 1989 (Australasian Region, keys, literature, distributions, bionomics).
acrostichalis Edwards, 1941 adami (Hamon & Mouchet, 1955) adersianus Edwards, 1941 albertianus Edwards, 1941 albiventris Edwards, 1922 amaniensis van Someren & Hamon, 1964 andreanus Edwards, 1927 baisasi Sirivanakarn, 1972 bokorensis Klein & Sirivanakarn, 1970 brenguesi Brunhes & Ravaonjanahary, 1973 brevipalpis (Giles, 1902) calabarensis Edwards, 1941 campilunati Carter & Wijesundara, 1948 castor de Meillon & Lavoipierre, 1944 castrensis Edwards, 1922 cataractarum Edwards, 1923 chauveti Brunhes & Rambelo, 1968 femineus Edwards, 1926 fimbriforceps Edwards, 1935 foliatus Brug, 1932 galliardi Edwards, 1941 garioui Bailly-Choumara & Rickenbach, 1966 germaini Geoffroy, 1974 hackeri Edwards, 1923 hamoni Brunhes, Adam & Bailly-Choumara, 1967 hayashii Yamada, 1917 helenae Brunhes, Adam & Bailly-Choumara, 1967 hinglungensis Chu, 1957 horridus Edwards, 1922 inconspicuosus (Theobald, 1908) insignis (Carter, 1911) iphis Barraud, 1924 jefferyi Sirivanakarn, 1977 kanyamwerima van Someren, 1951 khazani Edwards, 1922 kilara van Someren, 1951 kingianus Edwards, 1922 kiriensis Klein & Sirivanakarn, 1970 laplantei(Hamon, Adam & Mouchet, 1955) latifoliatus Delfinado, 1966 laureli Baisas, 1935 macrostylus Sirivanakarn & Ramalingam, 1976 malayensis Sirivanakarn, 1972 malayi (Leicester, 1908) manusensis Sirivanakarn, 1975 megafolius Chen & Dong, 1992 miaolingensis Chen, 1982 micolo Ribeiro, da Cunha Ramos, Capela & Pires, 1998 mijanae Brunhes, Adam & Bailly-Choumara, 1967 mohani Sirivanakarn, 1977 mundulus Grünberg, 1905 okinawae Bohart, 1953 oresbius Harbach & Rattanarithikul, 1988 orstom Brunhes, Adam & Bailly-Choumara, 1967 otachati Klein & Sirivanakarn, 1970 phangngae Sirivanakarn, 1972 pluvialis Barraud, 1924 pseudoandreanus Bailly-Choumara, 1966 quintetti Brunhes, Adam & Bailly-Choumara, 1967 rageaui (Hamon & Rickenbach, 1955) richardgarciai Jeffery, Oothuman & Rudnick, 1987 richei Klein, 1970 rima Theobald, 1901 rubinotus Theobald, 1906 ryukyuanus Tanaka, Mizusawa & Saugstad, 1979 selai Klein & Sirivanakarn, 1970 simplicicornis Edwards, 1930 simpliciforceps Edwards, 1941 stellatus van Someren, 1947 subrima Edwards, 1941 sunyaniensis Edwards, 1941 tauffliebi Geoffroy & Hervé, 1976 tenuipalpis Barraud, 1924 uncinatus Delfinado, 1966 vattieri Geoffroy, 1971 vinckei Hamon, Holstein & Rivola, 1957 wansoni Wolfs, 1945 wigglesworthi Edwards, 1941 yeageri Baisas, 1935