Anopheles boliviensis (Theobald, 1905), original combination: Kerteszia boliviensis.
Subfamily Anophelinae, genus Anopheles. Subgenus Kerteszia includes 12 species. Subgenus abbreviation – Ker.
Subgenus Kerteszia is most closely related to subgenus Nyssorhynchus. The two subgenera are very similar in overall morphology, but the following features easily distinguish the adults, larvae and pupae of Kerteszia. The scutum of adults has four distinct longitudinal lines of dark pollinose integument and a few scales in patches on the lateral and/or anterior areas. The scutellum is normally void of scales (a few rarely occur medially) and the mid- and hindfemora have a stripe of white scales on the distal third of their anterior surfaces. The wings are distinct in having crossveins sc-r and r1-rs relatively far apart (distance about half the length of the sector dark spot on the costa and radius-one), a spot of dark scales where the humeral crossvein intersects the radius, the subcosta ending before the subcostal pale spot, vein R4+5 dark-scaled apically, vein CuA mostly dark-scaled with a basal dark spot and the anal vein normally entirely dark-scaled (rarely wit one or two small pale spots). The gonocoxite, claspette and aedeagus of the male genitalia exhibit a number of differential and diagnostic features. The gonocoxite lacks a subapical seta, two subequal accessory setae are inserted beyond mid-length, the internal seta is very stout and inserted far basad of the accessory setae, and the parabasal seta is considerably longer than the internal seta. The ventral lobes of the claspette are narrowly joined separate structures, the dorsal lobes each bear two distinct groups of specialised setae, and the aedeagus is slender and uniformly tapered to a narrowly rounded apex. Larvae exhibit many distinctive features, which include, but are not limited to, seta 1-A single and inserted dorsolaterally, seta 2-C inserted on same level or slightly posterior to seta 3-C, seta 4-C inserted posterolateral to seta 3-C, hypostomal suture undeveloped or very short, absence of a sclerotised tubercle at the base of seta 4-C, long seta 4-M (about as long as seta 6-M), weakly plumose setae 8-M,T and 6,7-I,II, single seta 2 on segments I-IV, absence of seta 14-III, seta 2-IV inserted lateral to seta 4-IV, weakly developed seta 1-S (single, with 2 or 3 branches or weak terminal branches or aciculae) and nine pairs of seta 4-X. Salient features of Kerteszia pupae include a trumpet with a short pinna (less than half as long as the trumpet) and no meatal cleft, seta 9-I shorter than a third the length of seta 6-I, weakly developed setae 1-I-VII and 5-V-VII (less than half as long as the segment), seta 14-III absent, seta 2-IV,V inserted anterior and nearly in line with seta 3, seta 3-VI inserted lateral to seta 1-VI, seta 10-VI present and seta 1-Pa stout and shorter than seta 2-Pa (absent in An. neivai). See genus Anopheles.
With the exception of the molecular study of Freitas et al. (2015), phylogenetic studies of anopheline mosquitoes based on both morphological and molecular data support the monophyly of subgenus Kerteszia (Sallum et al., 2000, 2002; Collucci & Sallum, 2003; Harbach & Kitching, 2005, 2016; Foster et al., 2017). Except for the study of Foster et al., all of the studies that support the monophyly of the subgenus also support its sister relationship with subgenus Nyssorhynchus. Kerteszia was recovered as the sister to subgenus Stethomyia in the analyses of COI and COII mtDNA and 2.5S rDNA sequences conducted by Freitas et al., and was recovered in a sister relationship with Lophopodomyia in the study of Foster et al. based on analyses of mitochondrial protein coding genes. Collucci & Sallum (2003) explored the phylogenetic relationships of 12 species of Kerteszia, and Kirchgatter et al. (2020) examined the relationships of four species, two collected in Brazil and two collected in Peru.
The immature stages of species of Kerteszia, except those of An. bambusicolus, are found in water that accumulates in the leaf axils of terrestrial and epiphytic bromeliads. The immature stages of An. bambusicolus are normally found in unbroken bamboo internodes. The adults of Kerteszia are strongly anthropophilic. Peak biting activity occurs during the evening hours, but females are known to bite throughout the night, in the morning and in the shade during the daylight hours.
Six species of subgenus Kerteszia are known to transmit malarial protozoa, but only An. bellator in Trinidad and An. cruzii in Brazil are important vectors. Anopheles bellator also transmits the helminths that cause Bancroftian filariasis. Anopheles neivai and An. boliviensis have been found naturally infected with arboviruses, including yellow fever virus in the former species, and eggs of Dermatobia hominis have been found in the latter species.
Neotropical Region: south from Veracruz State in Mexico through Central America and Atlantic South America, along the Andes and along the coast, to the States of Misiones in Argentina and Rio Grande do Sul in Brazil, and also extends south along the Pacific Coast of South America to the State of El Oro, Ecuador. The subgenus is absent from all islands of the West Indies except Trinidad, and from most of the vast expanse of the Amazon basin in South America (Zavortink, 1973).
Komp, 1937 (taxonomy); Cova-Garcia, 1961 (Venezuela); Zavortink, 1973 (revision); Peyton et al., 1992 (morphology); Collucci & Sallum, 2003 (phylogeny); Harrison et al., 2012 (key to females); Lorenz et al., 2015 (An. cruzii and An. homunculus, characterisation, evolutionary relationships); Oliveira et al., 2016 (mitochondrial genomes); Foster et al., 2017 (phylogenetic relationships).
auyantepuiensis Harbach & Navarro, 1996
bambusicolus Komp, 1937
bellator Dyar & Knab, 1906
boliviensis (Theobald, 1905)
cruzii Dyar & Knab, 1908
gonzalezrinconesi Cova Garcia, Pulido F. & Escalante de Ugueto, 1977
homunculus Komp, 1937
laneanus Corrêa & Cerqueira, 1944
lepidotus Zavortink, 1973
neivai Howard, Dyar & Knab, 1913
pholidotus Zavortink, 1973
rollai Cova Garcia, Pulido F. & Escalante de Ugueto, 1977