The Anopheles albitarsis complex with the recognition of Anopheles oryzalimnetes Wilkerson and Motoki, n. sp. and Anopheles janconnae Wilkerson and Sallum, n. sp. (Diptera: Culicidae)

ARTICLES

The Anopheles albitarsis complex with the recognition of Anopheles oryzalimnetes Wilkerson and Motoki, n. sp. and Anopheles janconnae Wilkerson and Sallum, n. sp. (Diptera: Culicidae)

Maysa Tiemi Motoki^I; Richard C Wilkerson^II; Maria Anice Mureb SallumI, ⁺

^IDepartamento de Epidemiologia, Faculdade de Saúde Pública, Universidade de São Paulo, Avenida Dr. Arnaldo 715, 01246-904 São Paulo, SP, Brasil

^IIWalter Reed Army Institute of Research, Department of Entomology, Silver Spring, MD, USA

ABSTRACT

The Anopheles (Nyssorhynchus) albitarsis complex includes six species: An. albitarsis, Anopheles oryzalimnetes Wilkerson and Motoki, n. sp., Anopheles marajoara, Anopheles deaneorum, Anopheles janconnae Wilkerson and Sallum, n. sp. and An. albitarsis F. Except for An. deaneorum, species of the complex are indistinguishable when only using morphology. The problematic distinction among species of the complex has made study of malaria transmission and ecology of An. albitarsis s.l. difficult. Consequently, involvement of species of the An. albitarsis complex in human Plasmodium transmission is not clear throughout its distribution range. With the aim of clarifying the taxonomy of the above species, with the exception of An. albitarsis F, we present comparative morphological and morphometric analyses, morphological redescriptions of three species and description of two new species using individuals from populations in Brazil, Paraguay, Argentina and Venezuela. The study included characters from adult females, males, fourth-instar larvae, pupae and male genitalia of An. albitarsis, An. marajoara, An. deaneorum and An. oryzalimnetes n. sp. For An. janconnae n. sp. only characters of the female, male and male genitalia were analyzed. Fourth-instar larvae, pupae and male genitalia characteristics of all five species are illustrated. Bionomics and distribution data are given based on published literature records.

Key words: systematics - Nyssorhynchus - Anopheles albitarsis complex - new species - multivariate analysis

The Anopheles (Nyssorhynchus) albitarsis complex is widely distributed in South America and includes An. albitarsis Lynch-Arribálzaga, Anopheles deaneorum Rosa-Freitas, Anopheles marajoara Galvão and Damasceno, An. albitarsis B (Wilkerson et al. 1995c), An. albitarsis E (Lehr et al. 2005) and An. albitarsis F (Brochero et al. 2007). Three species are of proven importance as vectors of human malaria parasites in Brazil: An. deaneorum [state of Rondônia (RO)] (Klein et al. 1991a, b), An. marajoara [state of Amapá (AP)] (Conn et al. 2002) and An. albitarsis E [state of Roraima (RR)] (Póvoa et al. 2006).

Indications of the presence of a species complex in An. albitarsis s.l. were reported by Kreutzer et al. (1976) and Kitzmiller (1977) who found fixed chromosomal inversions suggesting the presence of two sympatric forms in Southern and Eastern Brazil and a third in Colombia and Venezuela. A similar conclusion was reached by Steiner et al. (1982) who used isozyme analyses of samples collected along a transect from state of São Paulo (SP) to west of Marajó Island to find three genetically distinct populations.

Linthicum (1988) recognized two species in the Albitarsis Complex, An. marajoara and An. albitarsis and provided characters for their identification. To better characterize the morphological characters of An. albitarsis s.s., Rosa-Freitas and Deane (1989) used specimens collected from the type locality of Baradero, Argentina, to designate a neotype and to redescribe the adult male and female, fourth-instar larva and pupa. Subsequently, Rosa-Freitas (1989) named and described An. deaneorum and distinguished it from An. albitarsis using morphological characteristics and evidence from allele frequencies of 11 allozyme loci. Morphological distinction of An. deaneorum from An. albitarsis and An. marajoara was based mainly on seta 3-C of the fourth-instar larva (multi-branched in An. deaneorum, single or aciculate in the other 2). Later, Narang et al. (1993) employed allozyme markers and Restriction Fragment Length Polymorphisms (RFLP) profiles of the mitochondrial genome to estimate genetic diversity of sympatric populations of An. deaneorum and An. marajoara from several localities in Brazil.

Wilkerson et al. (1995a, c) used random amplified polymorphic DNA polymerase chain reaction (RAPD-PCR) to show that the An. albitarsis complex included An. albitarsis, An. deaneorum, An. marajoara and An. albitarsis B. Recently, Lehr et al. (2005), based on the results of phylogenetic analyses of the mitochondrial cytochrome c oxidase subunit I (mtDNA COI) gene, proposed a fifth species in the complex, An. albitarsis E. In contrast, Li and Wilkerson (2005, 2006) observed consistent and diagnostic, but intragenomically variable differences in the ITS2 of the four species of An. albitarsis complex originally recognized with RAPDs, but the existence of An. albitarsis E was not corroborated. Using nucleotide sequences of the ITS2 rDNA and white gene from putative An. marajoara samples collected in Puerto Carreño, Colombia, Brochero et al. (2007) found yet another species, designated An. albitarsis F.

The above morphology, isoenzyme and DNA data clearly demonstrated that An. albitarsis was a species complex with component species involved in human malaria transmission. It is also clear that accurate species determinations are necessary to evaluate the vector status of each.

Multivariate analyses of measurements of morphological characteristics have been shown to be an effective method for distinguishing morphologically similar species, including medically important insects (Rubio-Palis et al. 1997, Rubio-Palis 1998, Calle et al. 2002). Considering that a primary objective of the present study was to discover means to identify five species of the An. albitarsis complex, we used principal component, discriminant and cluster analyses to assess morphological characters of the adult females. Additionally, we describe the adult males and females, fourth-instar larvae and pupae of An. albitarsis, An. marajoara, An. deaneorum and An. albitarsis B and adult females and males of An. albitarsis E.

MATERIALS AND METHODS

Adult female mosquitoes were collected in several localities in Brazil, Argentina, Paraguay and Venezuela (Table I) to obtain progeny broods of adult males and females with associated pupal and fourth-instar larval exuviae. At least one adult male or female of each progeny was used to identify the species using RAPD-PCR. Terminology for morphological characters follows Harbach and Knight (1980), except we used Belkin (1962) for wing veins and Wilkerson and Peyton (1990) for wing spots. The three life stages of An. albitarsis are described in detail; the other species of the complex were compared with An. albitarsis, but characteristics found to be identical were not included in their descriptions. For measurements and setal counts of the immatures, 10 slide-mounted specimens of each species were employed, unless otherwise indicated.

Specimens of each species, collected in widely separated localities of their known geographical range, were used in the morphometric analyses. Forty-one variables (Supplementary data) (39 wing spots plus the distance between the eyes and basal dark portion of hindtarsomere 2) were measured in 30 adult females of each species. Measurements were taken with a Wild stereomicroscope connected to a digital micrometric ocular Wild MMS 235^® (Heerbrugg, Switzerland).

Statistical analysis - The pattern of pale and dark spots on the wing veins, the distance between the eyes and the dark portion of hindtarsomere 2 were measured in 150 specimens, i.e., 30 specimens each of An. albitarsis, An. albitarsis B, An. marajoara, An. deaneorum and An. albitarsis E. Because dark and pale wing spots of the costal vein could be present or absent in individual specimens of a species, the absence of a spot influenced the recognition of flanking spots. Consequently, in the absence of a dark or pale spot, the adjacent spots could not be measured and thus scored as missing. Statistical analyses were performed with Minitab 14 for Windows XP and R-2.2.1 for Windows^® software program.

Descriptive statistics - Ranges, means and standard deviations of means were calculated for each quantitative variable. Normality and homogeneity tests were carried out to evaluate if data distribution was normal. Because of missing data, five variables that could have compromised the analyses were excluded. Boxplots were employed to display differences between measurements of variables.

Principal components analysis (PCA) - PCA was applied for the complete data set of 36 variables. This is a statistical analysis to reduce the dimensionality of a data set while retaining as much variation in the data as possible (Hugh & Gauch 1982). Principal component analysis was carried out as an intermediate step for understanding other analytical analyses. Because the first 13 principal components retained 80.1% of the variation present in 36-variable data set, they were used to obtain a new data set to carry out the discriminant function analysis.

Variance analysis (ANOVA) - ANOVA was applied to the 36-variable data set to verify if there were differences among the means of all variables (p > 0.05) of the five species and the equality hypothesis (H: μ₁ = μ₂ = μ₃ = μ₄ = μ₅) was tested. Because it was not possible to reject the equality hypothesis of two variables, these were excluded from discriminant function analysis.

Discriminant function analysis - Discriminant function analysis was applied to determine the possibility of segregation of all five previously determined species. Because of missing variables (Supplementary data), discriminant analyses were conducted in two rounds. Since in the first round missing data were excluded, we used the 23 remaining variables obtained from 126 specimens. In the second round, the first 13 principal component variables obtained in the PCA analysis were used to generate a new set of variables, which were used in the discriminant function analysis. A discriminant model was constructed using Fisher's linear discriminant analysis. Results of this analysis supported homogeneous covariance among five groups using cross validation.

Cluster analysis - Cluster analysis was employed using dissimilarity of variables (level = 41). Distances of each variable were entered for 150 specimens of five species. Based on the transformed data set of PCA, the discriminant analysis was applied to validate the results of the cluster analysis.

RESULTS

Morphometric analysis - Means and standard deviations for 41 variables were obtained from 150 specimens to compare five species of the An. albitarsis complex (Supplementary data). Both normality and homogeneity tests showed that all variables had a normal distribution. Because multivariate analysis considers only presence data those variables with missing information were excluded, i.e., presector dark, sector pale, accessory sector dark, first dark spot of CuA₁ and second pale spot of CuA₁.

Boxplot - The following characters, i.e., wing length, vein R₄₊₅ length and wing 3rd dark spot length of CuA₁, preapical dark, apical dark, sector dark and basal pale plus prehumeral pale spots showed upper median value (Fig. 1A-G), whereas accessory sector pale spot showed lower median value for An. albitarsis (Fig. 1H). Generally, specimens of An. albitarsis possess a longer wing than the others species of the complex. Wing accessory sector pale spot, 2nd dark spot of CuA₁ and 1st dark spot of R₄₊₅ showed upper median value for An. albitarsis B (Fig. 1H-J). An. deaneorum and An. albitarsis E showed the lowest median value of variables, although the subcostal pale spot of An. deaneorum (Fig. 1K) and 1st dark spot of CuA₁ and humeral dark of An. albitarsis E (Fig. 1L, M) showed upper median value. The subcostal pale spot and sector pale spot of An. albitarsis and An.albitarsis B are similar (Fig. 1K, N). The 2nd dark spot of CuA₁ of An. albitarsis and An. albitarsis E are similar (Fig. 1I). For An. marajoara, 50% of the lower median value of variables was similar to An. albitarsis and An. albitarsis B and 50% of the upper median value of variables was similar to An. deaneorum and An. albitarsis E. The boxplot indicates homogeneity variance of variables among five species of An. albitarsis complex.

PCA - The principal components analysis showed that the first 13 components retained 80.1% of the variation present in the 36-variable data set (Supplementary data).

ANOVA - All variables, except for the distance between the eyes and measurement of the presector pale spot (p <u>&gt;</u> 0.05), showed mean differences among the five species of the An. albitarsis complex. These two variables were therefore excluded from the discriminant analysis (Supplementary data).

Discriminant analysis - Discriminant analyses demonstrated that morphological variables might serve to discriminate the five species of the An. albitarsis complex (Supplementary data). In the first round, 96 (76%) of 126 specimens analyzed were correctly identified. In the second round, 112 (75%) of 150 specimens were correctly identified. A high percentage of discrimination was shown in An. albitarsis E when compared with the other species (1st round, 100% of 126 specimens; 2nd round, 97% of 150 specimens). The lowest percentage of discrimination was obtained for An. marajoara (1st round, 50%; 2nd round, 60%). Moreover, the percentage of correct discrimination for An. albitarsis, An. albitarsis B and An. deaneorum varied from 70-88%.

Cluster analysis - Cluster analysis based on the means of 36 variables revealed morphometric dissimilarities among the clusters. The specimens were clustered in two groups (Supplementary data), one comprising An. albitarsis and An. albitarsis B and the other formed by An. deaneorum and An. albitarsis E. Fifty-three percent of the specimens identified by RAPD-PCR as An. marajoara clustered in group one, whereas the other 47% clustered in group two. Results of the cluster analysis suggest that An. albitarsis and An. albitarsis B to be more similar to each other than to any other species of the complex. Similarly, An. deaneorum and An. albitarsis E clustered together, whereas An. marajoara could be differentiated in two distinct groups (Supplementary data). Results of the cluster analysis corroborated the results of the discriminant analysis (Supplementary data). The rate of correct discrimination was 83%.

An. albitarsis Lynch Arribálzaga

An. albitarsis Lynch Arribalzaga (1878): 150 (F). Type loc. Baradero, Buenos Aires, Argentina. Senevet (1934): 45 (P*); Pinto (1939): 345 (M*, F*, P*, L* E); Rozeboom (1942): 238 (E*, tax.); Ross and Roberts (1943): 31 (M*, F*, L*); Cova-Garcia (1946): 31, 83, 118 (E*, L*, F*, M*); Romeo-Viamonte and Castro (1951): 321 (F*); Garcia and Casal (1964) (1965): 6 (P*); Kreutzer et al. (1976): 473 (chromosomes); Rosa-Freitas and Deane (1989): 289 (M*, F*, P* L* E*, redescription, neotype desig., IOC-RJ); Wilkerson et al. (1995a, c): (RAPD-PCR, tax.). Anopheles limai Galvão and Lane (1937a): 227 (A, E*, as var.). Type loc. Pinheiros and Butantan, São Paulo, SP, Brazil. Type: not extant. Lane (1953): 244 (syn.); Belkin et al. (1971): 4 (tax.). Anopheles imperfectus Corrêa and Ramos (1943): 246 (F, as ssp). Type loc. Vera Cruz, SP{holotype [Faculdade de Saúde Pública, Universidade de São Paulo (FSP-USP)]}. Lane (1953): 244 (syn.); Belkin et al. (1971): 4 (tax.).

Female: head: integument brown to dark brown. Vertex and occiput with large erect white weakly forked truncate scales becoming dark laterally; anteriorly vertex with a few small obovate decumbent scales along upper orbital line and longer narrow white decumbent scales along interorbital line; ocular setae dark brown to black. Frontal tuft with long white setae. Clypeus bare. Pedicel of antenna brown to dark brown with decumbent white spatulate scales on dorsal surface; flagellomere 1 with semi-erect white scales on proximal 0.5 of medial surface and at apex of dorsal and lateral surfaces and patch of decumbent flat broad white scales at base of dorsal surface. Proboscis brown to dark brown with decumbent scales and short setae; length 2.00-2.14 mm (mean = 2.07 ± 0.04) (n = 10), 1.30-1.42 length of forefemur (mean = 1.36 ± 0.04) (n = 10), 0.98-1.12 length of maxillary palpus (mean = 1.04 ± 0.04) (n = 10). Labella similar to labium in color. Palpus 1.90-2.05 mm (mean = 1.99 ± 0.05) (n = 10), 0.88-1.01 length of proboscis (mean = 0.96 ± 0.04) (n = 10); palpomere 1 dark-scaled; palpomere 2 mostly dark-scaled with few white scales at apex of lateral and ventral surfaces; palpomere 3 mostly dark-scaled with sparse white scales on lateral surface and at apex of ventral surface; palpomere 4 mostly dark-scaled with white scales on median area of dorsal surface; palpomere 5 white-scaled; scales erect on palpomeres 1 and 2, semi-erect and decumbent on dorsal and lateral surfaces of palpomere 3, erect on ventral surface of palpomere 3, decumbent on palpomeres 4 and 5; length palpomere 2/palpus length 0.22-0.34 (mean = 0.28 ± 0.03) (n = 10); length palpomere 3/palpus length 0.30-0.38 (mean = 0.35 ± 0.02) (n = 10); length palpomere 4/palpus length 0.17-0.21 (mean = 0.19 ± 0.01) (n = 10); length palpomere 5/palpus length 0.11-0.14 (mean = 0.13 ± 0.01) (n = 10). Thorax: integument pruinose with darker areas between dorsocentral areas and lateral margin at posterior edge of scutal fossa, at posterior end of dorsocentral area, at posterior edge of scutum and posteriorly on prescutellar area, extending posteriorly onto median scutellar lobe; acrostichal, dorsocentral and prescutellar areas and scutal fossa with white spatulate decumbent scales, but not posteriorly on dark posterior bare area; supraalar and antealar areas with white spatulate decumbent scales; lateral margin of antealar area, extending posteriorly onto supraalar area, with elongate, narrow, semi-erect, white, spatulate scales; scutum bare anteriorly between acrostichal and dorsocentral areas, posteriorly to scutal fossa and posteriorly on prescutellar area; anterior promontory with erect piliform white scales; anterior lateral angle of scutum with erect broad spatulate white scales dorsally, dark scales ventrally. Scutellum with spatulate white scales posteriorly, posterior edge with row of long and few short pale brown setae with golden and reddish reflections. Mesopostnotum bare. Antepronotum with dark setae and patch of spatulate scales, these scales whitish dorsally, dark ventrally on upper area, remainder of antepronotum without scales but with scattered brown setae. Pleura with small patches of white spatulate scales on upper mesokatepisternum, posterior border of middle mesokatepisternum, upper region of prealar knob and upper mesepimeron; upper proepisternum, upper mesokatepisternum and prealar knob with dark brown setae; middle posterior border of mesokatepisternum, upper mesepimeron and prespiracular area with pale yellow setae. Wing: length 2.96-4.04 mm (mean = 3.35 ± 0.24) (n = 30); veins dark-scaled with spots of white scales on anterior area of costa, subcosta, R and R₁, pale yellow scales on remaining veins. Halter: scabellum with pale integument; pedicel with pale integument ventrally, dark dorsally with few white scales posteriorly on dorsal surface; capitellum pale-scaled ventrally, dark-scaled dorsally with patch of white scales at base. Legs: anterior surface of forecoxa with patch of spatulate scales mesally, these scales white laterally and dark medially and a few white spatulate scales ventrally, posterior surface of forecoxa with patch of ventrally directed black spatulate scales and patch of white scales laterally; outer surface of midcoxa with patches of white spatulate scales at apex on anterior and posterior surfaces and patch of white, spatulate, semi-erect scales at base; hindcoxa with patch of semi-erect white spatulate scales at apex and patch of white spatulate appressed scales at base of posterolateral surface. Fore, mid and hindtrochanters speckled with white and dark scales. Forefemur 1.49-1.56 mm (mean = 1.52 ± 0.02) (n = 10), 0.70-0.77 length of proboscis (mean = 0.73 ± 0.02) (n = 10); forefemur with light scales at base forming pale ring; anterior surface mostly dark brown, often with two narrow pale stripes along margins extending most of length of segment; posterior surface predominantly dark-scaled with few sparse white scales, apical 0.3 pale-scaled. Midfemur with pale and dark scales at base forming pale and dark rings; anterior surface mostly dark-scaled with longitudinal white stripe extending from base to near apex; one or two patches of white scales near apex; posterior surface entirely pale-scaled. Hindfemur with pale and dark scales at base forming pale and dark bands; dorsal surface mostly dark-scaled with preapical patch of white scales and small white patch at apex of anterodorsal surface, ventral surface pale-scaled. Tibiae dark-scaled with narrow longitudinal line of yellowish scales, posterior surface pale-scaled; all tibiae with white scales at apex. Tarsi with scales varying in color from white to yellowish to dark. Foretarsomeres 1, 2 and 3 predominantly dark-scaled with pale scales at apex; tarsomeres 4 and 5 normally dark-scaled. Midtarsomeres 1 and 2 predominantly dark-scaled with apical patches of pale scales; tarsomeres 3 and 4 dark-scaled, sometimes with pale scales apically; tarsomere 5 dark-scaled with apical pale scales on dorsal surface. Hindtarsomere 1 dark-scaled with longitudinal stripe of yellowish scales extending from near base to apex of tarsomere; tarsomere 2 dark-scaled proximally with basal dark band 0.52-0.86 length of tarsomere (mean = 0.62 ± 0.08) (n = 30); tarsomeres 3, 4 and 5 white-scaled. Abdomen: tergum I with numerous long brown setae, without caudolateral scale-tufts; tergum II with numerous brown setae, medially with numerous pale yellow to whitish scales extending laterally on posterior area, without caudolateral scale-tufts, sometimes present on tergum III, caudolateral tufts on tergum III with few dark erect scales extending laterally; terga IV-VII with numerous pale yellow to whitish scales medially and dark scales laterally on posterior margin, caudolateral tufts always present, with large dark erect scales extending laterally; tergum VIII with numerous, light yellow scales basally, white scales apically, usually with dark scales posterolaterally, without caudolateral tufts. Sternum I with submedian stripes of white scales; sterna II-VII with numerous dark setae, shorter than those on terga and longitudinal patches of white scales lateral of midline and small patches of dark scales posterior on midline; sternum VIII with longitudinal patches of white scales lateral of midline and with dark scales on midline.

Male: similar to female except for sexual differences. Maxillary palpus pale and dark-scaled; scales semi-erect on basal 0.5 of palpomere 2, decumbent on remainder of palpomere 2 and on palpomeres 3-5; palpomere 2 dark-scaled with pale scales at apex; palpomere 3 with pale scales at base and with pale spot dorsally on medial surface, apex with long setae; palpomere 4 with pale scales on ventral and dorsal surfaces, dark-scaled at apex and base; palpomere 5 with dark setae along ventral surface and pale scales dorsally, dark scales ventrally and basally.

Male genitalia (Fig. 2): segment IX (not shown): sternum rectangular, median posterior border emarginate, anterior border weakly emarginate. Gonocoxite elongate; tergal surface with 3-6 tergomedial setae, one apicolateral seta and one apicomedial seta; dorsomedial rim 0.09-0.12 (mean = 0.1 ± 0.01) (n = 5) length of gonocoxite; tubercle of parabasal seta 0.22-0.41 (mean = 0.32 ± 0.06) (n = 5) length of parabasal seta; accessory setae 0.33-0.41 (mean = 0.36 ± 0.03) (n = 5) length of gonocoxite; internal seta subequal to ventralmost accessory seta. Dorsal claspette with narrow, curved pedicel, rounded at base, apical setae moderately broad, strongly curved mesally, without noticeable basomesal projection. Ventral claspette (in ventral aspect) with apex moderately wide and strongly striated, single, rounded lobe expanded ventrally; preapical plate absent; basal lobules laterally expanded. Gonostylus slender, curved with row of minute setae inserted before gonostylar claw. Aedeagus cylindrical approximately 0.39-0.47 (mean = 0.43 ± 0.03) (n = 4) length of gonocoxite, apex rounded, wider than long, ventromesal subtriangular projections connecting at midline, leaflets absent.

Pupa (Fig. 2): position and development of setae as figured; range and modal number of branches in Table II. All measurements were made on 10 specimens unless otherwise indicated. Cephalothorax: integument and legs weakly pigmented; trumpet angusticorn with meatal cleft; pinna moderately pigmented; meatal cleft U-shaped basally. Abdomen: length 2.50-3.11 mm (mean = 2.84 ± 0.20); seta 3-I usually single, 5-I single to triple, 6-I single or double, 9-I usually single, sometimes double, as long as 6-I; 0-II-VII moderately developed, 6-II single or double, 1.12-2.52 length of 7-II (mean = 1.76 ± 0.51), 9-II min, unpigmented, 9-II-IV less than 0.20 length of segment; 6-III, IV normally double, 9-III short, stout, 1.11-2.50 (mean = 1.67 ± 0.45) length of 9-II; 1-IV-VII always single, strong, long, extending beyond caudal border of following segment, 3-IV with branches extending beyond caudal margin of segment, 9-IV thick, 1.35-2.82 (mean = 2.01 ± 0.49) length of 9-III, 10-IV, V always single; 0-V-VII often 4-branched, 3-V with branches extending well beyond caudal margin of segment, 8-V, VI frequently double, 9-V dark, strong, curved, 1.68-3.09 (mean = 2.38 ± 0.47) length of 9-IV, 9-V, VI less than 0.50 length of segment; 7-VI usually single, rarely double, 9-VI strong, curved, 1.10-1.64 (mean = 1.28 ± 0.16) length of 9-V; 9-VII strong, curved, sharply pointed, 0.98-1.86 (mean = 1.42 ± 0.26) length of 9-VI; seta 10-IV absent; 9-VII, VIII about 0.50 length of segment; 0-VIII normally single, 9-VIII straight, 0.66-1.10 (mean = 0.85 ± 0.15) length of 9-VII. Male genital lobe: thick at base with sides tapering toward apex, apex with mammiliform protuberance. Paddle obovate, 1.24-1.47 (mean = 1.37 ± 0.06) longer than wide, length 0.70-0.85 mm (mean = 0.78 ± 0.05), width 0.49-0.62 mm (mean = 0.57 mm ± 0.04), refractile index 0.70-0.78 (mean = 0.73 ± 0.03), outer margin distal to buttress including apex with very fine, minute spicules, inner margin smooth; seta 2-Pa usually single.

Fourth-instar larva (Fig. 3): position and development of setae as figured; range and modal number of branches in Table III. Measurements were made on 10 specimens unless otherwise indicated. Head: length 0.62-0.76 mm (mean = 0.66 mm ± 0.06) (n = 5), width 0.58-0.69 mm (mean = 0.62 ± 0.05) (n = 5). Integument weakly pigmented with darker spots along posterior border of dorsal apotome, on posterior margin of frontal ecdysial line on lateralia, posteriorly on lateral area of lateralia, ventrally on lateralia, on anterior area of labiogula and along hypocranial ecdysial line. Dorsomentum strongly sclerotized, blackish, median tooth moderately broad, tapered to point and blunt at apex, about twice as wide as adjacent tooth. Antenna: length 0.27-0.35 mm (mean = 0.31 mm ± 0.02), 7.36-8.83 (mean = 8.26 ± 0.52) longer than wide, with long thin spicules on mesal margin, spicules short and sparse on dorsal and ventral surfaces, seta 1-A, 0.25-0.34 (mean = 0.28 ± 0.03) distance from base. Seta 2-C single with minute, sparse aciculae, 1.14-1.53 length of 3-C (mean = 1.35 ± 0.11), distance between bases 3.76-6.59 (mean = 4.85 ± 0.77) width of base of single seta, 3-C single, 0.65-0.87 length of 2-C (mean = 0.74 ± 0.06), clypeal index 0.78-1.79 (mean = 1.38 ± 0.26) (distance between bases of 2-C and 3-C on one side/distance between the bases of 2-C), seta 4-C branched, short, extending 0.5 distance to anterior margin of head, 10-C triple. Collar dark brown, moderately wide dorsolaterally. Thorax: seta 1-P with apically truncate leaflets, 14-P with long branches arising from short shaft, median branches longer than lateral branches, extending beyond anterior margin of thorax; 1-M plumose; 2-T moderately long, single, extending beyond caudal margin of thorax, 3-T palmate, with narrow leaflets. Abdomen: integument with minute spicules on ventral surface of segments II-VIII; seta 5-I with branches arising from short stem less than length of seta from lateral margin of abdomen; 0-II-VII large, multibranched, 1-II-VII with variable truncate to pointed leaflets, 2-II, III large with strongly developed branches; 2-IV rarely double,13-IV extending to caudal margin of segment; 2-V normally single, 13-V extending beyond caudal margin of segment. Pecten with 3-5 long, 11-14 short spines, long spines 2.45-2.98 (mean = 2.70 ± 0.16) length of short spines; lateral arms of median plate of spiracular apparatus short to moderately long. Segment X covered with spicules, those on posterior margin stronger, seta 1-X longer than length of saddle, inserted on or off saddle, anal papillae longer than saddle.

Distribution - Distribution data presented here are from the published literature records referring to specimens of An. albitarsis identified by RAPD-PCR, mtDNA-COI or rDNA-ITS2. An. albitarsis is found in Argentina, Provinces of Misiones, Corrientes and Buenos Aires; Brazil, states of Santa Catarina, Paraná (PR) and SP (Wilkerson et al. 1995c, Lehr et al. 2005, Li & Wilkerson 2005); and Paraguay, state of Alto Paraná (Wilkerson et al. 1995c).

Material examined - Table I.

Type data - An. imperfectus, holotype, Vera Cruz, SP (GR Ramalho coll. (1939), Corrêa and Ramos (1943), det., pinned adult female in moderately good condition, inside a glass vial, collection number E-1265, FSP-USP, SP.

Bionomics - Kakitani and Forattini (2000) observed that the daily survival rate for An. albitarsis (as An. albitarsis B) is 0.5566 ± 0.015 and that the duration of the gonotrophic cycle is 2,046 days in the Ribeira Valley, in the southeastern part of SP. Lounibos et al. (1998) observed that under laboratory conditions 22.9% of nulliparous females of An. albitarsis failed to mature eggs after one blood meal.

An. albitarsis seems to be adapted to human environments. Results of collections carried out using Shannon traps in irrigated rice fields showed that there was an increase in both An. albitarsis A and An. albitarsis B densities that could be associated with the development of rice farming. At the same area, An. albitarsis fed on humans indoors and outdoors, at sunset and sunrise, in a domestic environment (Forattini et al. 1995).

Medical importance - Because of misidentification of members of the An. albitarsis complex, the medical importance of An. albitarsis is unknown.

Molecular characterization - An. albitarsis can be recognized by a RAPD-PCR profile produced using Operon primers B16, A01 and C15 (Wilkerson et al. 1995a, c). However, this method can be unreliable as an identification tool because results might differ depending on the DNA extraction protocol, reagents and type of PCR thermocycler (Li & Wilkerson 2005). A preferable method of identification is the use of a combination of species-specific primers based on rDNA ITS2 sequence developed by Li and Wilkerson (2005). Lehr et al. (2005) and Wilkerson et al. (2005) corroborated the monophyly of An. albitarsis when using COI mtDNA sequence data and combined COI, ND4 mtDNA, ITS2, 28S rDNA sequence data, respectively.

Anopheles marajoara Galvão and Damasceno

Anopheles marajoara Galvão and Damasceno (1942): 424 (M, F, L). Type: holotype, adult male with associated fourth instar larval and pupal exuviae (FSP-USP). Type loc. Santa Maria Farm, 400 m distant from Camará River, between Cachoeira do Arari and Salvaterra municipalities, Ilha de Marajó, Pará (PA), Brazil. Lane (1953): 244 (syn.); Belkin et al. (1971): 4,46 (type info, tax.); Linthicum (1988): 198 (from syn. with An. albitarsis); Quiñones and Suarez (1990): 602-604 (biology); Lounibos and Conn (1991): 57-66 (biology); Narang et al. (1993): 97-112 (tax., cryptic species); Rubio-Palis (1995): 482-484 (feeding behavior); Wilkerson et al. (1995c): 697-704 (tax., RAPD-PCR); Chadee and Wilkerson (2006): 22-28 (ecology, feeding behavior); Senise et al. (2006): 453-457 (type info, exclusion of the male genitalia slide associated with the holotype from the type material). An. albitarsis domesticus Galvão and Damasceno (1944): 78 (M, F, E*). Type loc. Cachoeira do Arari, Ilha de Marajó, PA. Correa et al. (1950): 280 (biology); Belkin et al. (1971): 4 (type info); Rios et al. (1984): 461 (tax.); Linthicum (1988): 198 (syn. with An. marajoara).

Female: similar to An. albitarsis except as follows. Proboscis brown to dark brown with decumbent scales and short setae; length 1.92-2.05 mm (mean = 1.97 mm ± 0.05) (n = 5), 1.28-1.41 length of forefemur (mean = 1.34 ± 0.05) (n = 5), 1.00-1.07 length of maxillary palpus (mean = 1.04 ± 0.03) (n = 5). Labella similar in color to labium. Palpus 1.85-1.97 mm (mean = 1.91 ± 0.06) (n = 5), 0.93-1.00 length of proboscis (mean = 0.96 ± 0.02) (n = 5); length palpomere 2/palpus length 0.26-0.32 (mean = 0.29 ± 0.02) (n = 5); length palpomere 3/palpus length 0.32-0.37 (mean = 0.34 ± 0.02) (n = 5); length palpomere 4/palpus length 0.16-0.21 (mean = 0.18 ± 0.01) (n = 5); length palpomere 5/palpus length 0.13-0.15 (mean = 0.13 ± 0.01) (n = 5). Wing: length 2.72-3.60 mm (mean = 3.14 ± 0.22) (n = 30); veins dark-scaled with spots of white scales on anterior area of costa, subcosta and R and R₁, pale yellow scales on remaining veins. Forefemur 1.40-1.60 mm (mean = 1.49 mm ± 0.08) (n = 5), 0.71-0.78 length of proboscis (mean = 0.75 ± 0.03) (n = 5); hindtarsomere 2 dark-scaled proximally with a basal dark band 0.40-0.63 length of tarsomere (mean = 0.49 ± 0.06) (n = 30).

Male: similar to An. albitarsis.

Male genitalia (Fig. 4): similar to An. albitarsis except for the characters as follow. Tubercle of parabasal seta 0.22-0.25 (mean = 0.23 ± 0.04) (n = 3) length of parabasal seta; dorsomedial rim 0.10-0.13 (mean = 0.11 ± 0.01) (n = 3) length of gonocoxite; dorsal accessory setae 0.35-0.42 (mean = 0.38 ± 0.03) (n = 3) length of gonocoxite; aedeagus 0.41-0.45 (mean = 0.42 ± 0.01) (n = 3) length of gonocoxite.

Pupa (Fig. 4): similar to An. albitarsis except as follows. Position and development of setae as figured; range and modal number of branches in Table IV. All measurements were made on 10 specimens. Abdomen: length 2.43-3.26 mm (mean = 2.74 mm ± 0.26); 3-I single to triple, 9-I always single; 6-II single or double, 1.19-2.99 length of 7-II (mean = 1.99 ± 0.50); 6-III-V usually double, 9-III 1.20-2.59 (mean = 1.93 ± 0.51) length of 9-II; 5-IV usually triple, 8-IV-VI single to triple, 9-IV 1.40-2.70 (mean = 1.87 ± 0.42) length of 9-III, 10-IV, V always single, long; 0-V-VII often 5-branched, 9-V 1.83-3.99 (mean = 2.45 ± 0.65) length of 9-IV, 9-V, VI less than 0.5 length of segment; 5-VI with 1-3 branches, 7-VI, VII single or double, 9-VI 0.93-2.18 (mean = 1.32 ± 0.34) length of 9-V; 5-VII single, 9-VII 1.17-1.79 (mean = 1.38 ± 0.20) length of 9-VI, 9-VII,VIII about 0.5 length of segment; 0-VIII normally single (1-4 branches), 9-VIII 0.82-1.04 (mean = 0.90 ± 0.08) length of 9-VII, 4-VIII double or triple. Paddle 1.14-1.45 (mean = 1.34 ± 0.08) longer than wide, length 0.65-0.79 mm (mean = 0.73 mm ± 0.04), width 0.45-0.66 mm (mean = 0.55 mm ± 0.06), refractile index 0.67-0.75 (mean = 0.71 ± 0.03).

Fourth-instar larva (Fig. 5): similar to An. albitarsis except as follows. Position and development of setae as figured; range and modal number of branches in Table V. Measurements were made on 10 specimens unless otherwise indicated. Head: length 0.59-0.75 mm (mean = 0.68 ± 0.05), width 0.65-0.82 mm (mean = 0.73 ± 0.06) (n = 9). Integument with darker spots on central area of dorsal apotome, along frontal ecdysial line and on lateral and ventral areas of lateralia, labiogula with two pale spots between hypostomal suture and hypocranial ecdysial line. Antenna: length 0.27-0.38 mm (mean = 0.31 mm ± 0.03), 7.55-8.91 (mean = 8.12 ± 0.39) longer than wide, weakly to strongly pigmented (specimens from SP); seta 1-A with branches 0.25-0.34 (mean = 0.30 ± 0.03) distance from base. Seta 2-C 1.24-1.55 length of 3-C (mean = 1.42 ± 0.09), distance between bases of 2-C 3.91-6.05 (mean = 4.92 ± 0.66) width base of single seta, 3-C moderately aciculate, 0.65-0.81 length of 2-C (mean = 0.71 ± 0.05), clypeal index 0.97-1.66 (mean = 1.17 ± 0.22), 9, 10-C often triple. Thorax: seta 1-P palmate, with leaflets truncate at apex. Abdomen: seta 13-I, III often 5-branched; 0-II-VII large, multibranched, 1-II-VII with truncate to pointed leaflets; 2-IV single or double, 2-V long, always single, 13-IV, V often 4-branched. Pecten with 4-5 long, 10-14 short spines, long spines 2.53-3.71 (mean = 3.04 ± 0.30) length of short spines; lateral arm of median plate of spiracular apparatus short to moderately long. Segment X: seta 1-X inserted on or off saddle.

Distribution - An. marajoara is found in Brazil, states of Mato Grosso (MT), Amazonas (AM), SP, PA and RO (Wilkerson et al. 1995a, c, Lehr et al. 2005, Li & Wilkerson 2005) and AP (Conn et al. 2002, Li & Wilkerson 2005); Paraguay, state of Alto do Paraná (Wilkerson et al. 1995c). Records from RR, and Departments of Zulia, Cojedes and Barinas, Venezuela (Wilkerson et al. 1995a, Rubio Palis 2003, Li & Wilkerson 2005) may refer to Anopheles janconnae n. sp An. marajoara is so far the only species of the complex found in Trinidad (Chadee & Wilkerson 2006).

Material examined - Table I.

Bionomics - Since a new species related to An. marajoara, An. albitarsis F, has been recognized in Colombia by Brochero et al. (2007), published literature records in Colombia and neighboring countries may refer to An. marajoara, An. albitarsis F or An. janconnae n. sp. Until the distributions of these species are better known caution should be exercised when interpreting the literature referring to An. marajoara.

Conn et al. (2002) conducted entomological surveys in malaria areas of Macapá, AP, and found An. marajoara frequently infected, replacing Anopheles darlingi as the primary vector. It is hypothesized that the observed change in mosquito population densities was caused by deforestation for agriculature that resulted in newly created ground pools favoring An. marajoara larvae. In a study carried out in Ilha Comprida, Atlantic Forest domain, southern SP, Kakitani et al. (2003) observed that the biting activity of An. marajoara peaked between 2-5 h. In contrast, Chadee (1992) found that An. marajoara from Trinidad showed extra-domiciliary and intra-domiciliary biting behavior, with host-seeking activity starting at 17 h and ending at 22 h. They recommended, because of the differences in the peak activity for An. marajoara from Southern Brazil and Trinidad, that these populations should be more closely investigated to determine if they represent distinct species.

Medical importance - Historically, An. marajoara was thought to be at most a secondary local vector of malarial parasites (Linthicum 1988). However, recent published data show that An. marajoara is a primary vector of human malarial parasites in Macapá (Conn et al. 2002) and Serra do Navio, AP (Póvoa et al. 2001).

Molecular characterization - An. marajoara can be recognized by RAPD-PCR banding profiles produced by Operon primers D01, A01, C19 and C16 (Wilkerson et al. 1995a, c). Similarly, Li and Wilkerson (2005) demonstrated that An. marajoara can be distinguished from other species of the complex by species specific ITS2 sequence. Lehr et al. (2005), using COI mtDNA sequence data, found at least two species under the name An. marajoara among specimens that were first identified by the RAPD-PCR profile and ITS2 sequence. Consequently, using the results of phylogenetic analyses, Lehr et al. (2005) hypothesized a fifth species, An. albitarsis E, which had been identified as An. marajoara. Wilkerson et al. (2005) using ND4, COI, ITS2 and 18S sequence data recovered a nonexclusive clade consisting of individuals of An. marajoara and An. deaneorum. Lack of exclusivity of sequences of An. marajoara and An. deaneorum was considered suggestive of ancestral introgression or perhaps a recent speciation event. Merritt et al. (2005) used coding sequence of the white gene including its fourth intron, to examine relationships among five species of the An. albitarsis complex. Results of sequence analyses showed the presence of the fourth intron in An. marajoara, whereas it is absent in the other species of the complex. Phylogenetic placement of An. marajoara within the complex was not entirely resolved because Wilkerson et al. (2005) found high support for a close relationship between An. marajoara and An. deaneorum, while Merritt et al. (2005) found support for An. marajoara sister to An. albitarsis B.

Anopheles (Nyssorhynchus) deaneorum Rosa-Freitas

An. deaneorum Rosa-Freitas (1989): 535 (M, F*, P, L*, E). Type: holotype, adult female with associated fourth instar larval and pupal exuviae (IOC-RJ). Type locality: Palheta, Guajará-Mirim, RO. Klein et al. (1990): 510-513 (tax., biology); Klein et al. (1991c): 301-303 (tax., DNA hybridization); Narang et al. (1993): 97-112 (tax., allozyme, RFLP); Wilkerson et al. (1995c): 697-704 (tax., RAPD-PCR).

Female: similar to An. albitarsis except as follows. Proboscis brown to dark brown with decumbent scales and short setae; length 1.75-1.92 mm (mean = 1.82 mm ± 0.05) (n = 8), 1.28-1.39 length of forefemur (mean = 1.33 ± 0.03) (n = 8), 1.06-1.16 length of maxillary palpus (mean = 1.10 ± 0.04) (n = 8). Labella similar in color to labium. Maxillary palpus 1.57-1.76 mm (mean = 1.67 mm ± 0.06) (n = 8), 0.86-0.95 length of proboscis (mean = 0.91 ± 0.04) (n = 8); length palpomere 2/palpus length 0.26-0.31 (mean = 0.30 ± 0.02) (n = 8); length palpomere 3/palpus length = 0.28-0.38 (mean = 0.33 ± 0.03) (n = 8); length palpomere 4/palpus length = 0.16-0.22 (mean = 0.18 ± 0.02) (n = 8); length palpomere 5/palpus length = 0.13-0.16 (mean = 0.14 ± 0.01) (n = 8). Wing: length 2.80-3.60 mm (mean = 3.17 ± 0.19) (n = 30); veins dark-scaled with spots of white scales on anterior area of costa, subcosta and R and R₁, pale yellow scales on remainder of veins. Forefemur 1.30-1.43 mm (mean = 1.37 ± 0.04) (n = 8), 0.72-0.78 length of proboscis (mean = 0.75 ± 0.02) (n = 8); hindtarsomere 2 dark-scaled proximally with basal dark band 0.51-0.90 length of tarsomere (mean = 0.67 ± 0.08) (n = 30). Abdomen: posterolateral tufts of scales absent from tergum III.

Male: similar to An. albitarsis. Abdomen: caudolateral tufts always absent from tergum III, tergum IV with few dark, erect caudolateral scales, terga V-VII with caudolateral scale tufts.

Male genitalia (Fig. 6): similar to An. albitarsis except as follows. Tubercle of parabasal spine 0.24-0.44 (mean = 0.34 ± 0.09) (n = 2) length of parabasal spine; dorsomedial rim 0.08-0.10 (mean = 0.09 ± 0.01) (n = 3) length of gonocoxite; dorsal accessory setae 0.35-0.39 (mean = 0.37 ± 0.02) (n = 3) length of gonocoxite; aedeagus 0.41-0.46 (mean = 0.44 ± 0.02) (n = 3) length of gonocoxite.

Pupa (Fig. 6): similar to An. albitarsis except as follows. Position and development of setae as figured; range and modal number of branches in Table VI. All measurements were made on 10 specimens. Abdomen: length 2.54-3.04 mm (mean = 2.77 ± 0.16); 3-I usually single; 0-II-IV normally 6-branched, 6-II 1-4 branched, 1.25-2.74 length of 7-II (mean = 1.99 ± 0.50), 9-II min, unpigmented, 9-II-IV less than 0.25 length of segment; 8-III, IV normally triple, 9-III short, stout, 0.91-3.22 (mean = 2.22 ± 0.74) length of 9-II; 1-IV rarely double, 6-IV-VI single to triple, 9-IV 1.51-3.96 (mean = 2.44 ± 0.74) length of 9-III, 10-IV, V always single, long; 0-V,VI usually with five branches, 3-V single to 6-branched, 5-V, VI with 1-4 branches; 5-VII single or double, rarely double, 7-V normally 3-branched, 8-V,VI often double, 9-V 1.23-2.07 (mean = 2.08 ± 0.43) length of 9-IV, 9-V, VI less than 0.50 length of segment; 7-VI,VII often single, 9-VI 1.11-2.24 (mean = 1.35 ± 0.33) length of 9-V; 5-VII rarely double, 9-VII, VIII less than 0.60 length of segment, 9-VII, 1.05-1.38 (mean = 1.19 ± 0.10) length of 9-VI; 9-VIII 0.82-1.19 (mean = 0.97 ± 0.11) length of 9-VII. Paddle 1.32-1.47 (mean = 1.37 ± 0.04) longer than wide, length 0.69-0.83 mm (mean = 0.76 mm ± 0.04), width 0.47-0.63 mm (mean = 0.56 mm ± 0.04), refractile index 0.69-0.78 (mean = 0.74 ± 0.03); 2-Pa usually double.

Fourth-instar larva (Fig. 7): similar to An. albitarsis except as follows. Position and development of setae as figured; range and modal number of branches in Table VII. Measurements were made on 10 specimens unless otherwise indicated. Head: length 0.65-0.73 mm (mean = 0.71 ± 0.03) (n = 6), width 0.61-0.66 mm (mean = 0.65 ± 0.02) (n = 6). Integument weakly pigmented with darker spots along posterior border of dorsal apotome, on posterior margin of frontal ecdysial line, on lateralia and on ventral lateralia, labiogula darkened along hypocranial ecdysial line and hypostomal suture. Antenna: length 0.28-0.34 mm (mean = 0.31 mm ± 0.02), 7.38-8.78 (mean = 8.21 ± 0.52) longer than wide; seta 1-A insertion 0.26-0.34 (mean = 0.30 ± 0.03) distance from base, seta 2-A with minute spicules on mesal margin. Seta 2-C 1.21-1.41 length of 3-C (mean = 1.28 ± 0.07), seta 2-C relatively far from mate of opposite side, distance between bases 4.10-7.06 (mean = 5.55 ± 0.83) width base of single seta, 3-C 0.71-0.83 length of 2-C (mean = 0.78 ± 0.04), clypeal index 0.76-1.29 (mean = 1.02 ± 0.14), seta 4-C single to 6-branched. Thorax: leaflets of 1-P pointed to truncate at apex. Abdomen: seta 13-I, III often 5-branched; 0-II-VII multibranched, 1-II-VII with truncate to pointed leaflets; 2-IV, V single, long. Pecten with 3-5 long, 9-13 short spines, long spines 2.36-3.24 (mean = 2.68 ± 0.28) length of short spines. Segment X: seta 1-X longer than length of saddle, inserted on or off saddle.

Distribution - An. deaneorum is found in the Province of Corrientes, Argentina (Wilkerson et al. 1995a, Li & Wilkerson 2005). In Brazil, the species was recorded in PR and RO (Wilkerson et al. 1995a, Li & Wilkerson 2005) and Acrelândia municipality, state of Acre (MAM Sallum 2008, personal communication).

Material examined - Table I.

Bionomics - Klein et al. (1991d) compared the biting behavior of Anopheles mosquitoes in Costa Marques, RO, and found that An. deaneorum and An. darlingi are more anthropophilic than other anophelines at that site. Also, both species were more frequent inside houses than other Anopheles species. An. deaneorum was also collected on human bait outside and inside houses (6% and 9% of anophelines captured, respectively) in Costa Marques, RO (Klein & Lima 1990).

Medical importance - An. deaneorum is considered to be a potential vector of human malarial parasites in RO (Klein et al. 1991b, c). Klein et al. (1991a) compared the susceptibility of five anopheline mosquitoes to Plasmodium falciparum in RO, and demonstrated that the oocyst positive rate and the mean number of oocysts in An. deaneorum are similar to those found in sympatric An. darlingi. The salivary gland sporozoite rate was similar to that found in Anopheles mediopunctatus s.l. when compared to An. darlingi. However, the susceptibility to P. falciparum was lower for An. deaneorum when compared to An. darlingi (Klein et al. 1991b). For Plasmodium vivax, the salivary gland infection rate in An. deaneorum was similar to that found in An. darlingi. In An. deaneorum, monoclonal antibodies for circumsporozoite proteins gave the following positive results: P. falciparum, 2.76%; P. vivax, 0.55%; P. vivax VK247, 0.82%; and Plasmodium malariae, 0.0% (Branquinho et al. 1993). Also, P. vivax-like parasites were reported from two out of 168 An. deaneorum tested using serological tests (Marrelli et al. 1998).

Molecular and morphological characterization - An. deaneorum is the only species of the An. albitarsis complex that can be recognized morphologically by the distinctly branched fourth-instar larval seta 3-C, which is single and simple or aciculate in An. albitarsis, An. marajoara and Anopheles oryzalimnetes n. sp. Rosa-Freitas (1989) suggested that the absence of posterolateral scales on the third abdominal segment of the adult female could be employed to distinguish An. deaneorum. However, this character is variable and the scales are easily lost when specimens are not adequately preserved. An. deaneorum can be recognized by diagnostic bands of the RAPD-PCR profile produced using Operon primers D01, C15, B11, A12 and A08 (Wilkerson et al. 1995a, c). In addition, Li and Wilkerson (2005) demonstrated that An. deaneorum could be distinguished from other species of the complex by species-specific ITS2 sequence. Lehr et al. (2005), using COI mtDNA sequence data, found that An. deaneorum clustered together in a strongly or moderately supported monophyletic lineage in a clade that includes An. marajoara. Consequently, Lehr et al. (2005) hypothesized that, either An. marajoara could consist of at least two phylogenetic species or An. deaneorum and An. marajoara were not valid species. Similar results were obtained by Wilkerson et al. (2005) in phylogenetic analyses employing the position 3 partition of the COI and ND4 mtDNA sequences.

Anopheles (Nyssorhynchus) oryzalimnetes Wilkerson and Motoki, n. sp.

An. albitarsis species B Wilkerson et al. (1995c): 699; Wilkerson et al. (1995a): 721. An. albitarsis A of Forattini et al. (1995): 21; Forattini et al. (1996): 299; Kakitani and Forattini (2000): 33.

Etymology - the name oryzalimnetes is a combination of oryza, Greek for rice and limnetes, Greek for inhabiting or born in a lake or marsh. This mosquito species was first found in a rice plantation.

Female: similar to An. albitarsis except as follows. Proboscis brown to dark brown with decumbent scales and short setae, length 1.98-2.25 mm (mean = 2.07 ± 0.10) (n = 6), 1.28-1.44 length of forefemur (mean = 1.40 ± 0.04) (n = 6), 1.02-1.14 length of maxillary palpus (mean = 1.06 ± 0.04) (n = 6). Labella similar in color to labium. Palpus 1.90-2.00 mm (mean = 1.96 ± 0.03) (n = 6), 0.88-0.98 length of proboscis (mean = 0.95 ± 0.04) (n = 6); length palpomere 2/palpus length 0.27-0.30 (mean = 0.29 ± 0.01) (n = 6); length palpomere 3/palpus length 0.32-0.37 (mean = 0.35 ± 0.02) (n = 6); length palpomere 4/palpus length 0.16-0.20 (mean = 0.18 ± 0.02) (n = 6); length palpomere 5/palpus length 0.12-0.15 (mean = 0.13 ± 0.01) (n = 6). Wing: length 3.02-3.54 mm (mean = 3.27 ± 0.14) (n = 30); veins dark-scaled with spots of white scales on anterior area of costa, subcosta, R and R₁, pale yellow scales on remaining veins. Forefemur 1.43-1.57 mm (mean = 1.48 ± 0.05) (n = 6), 0.69-0.75 length of proboscis (mean = 0.72 ± 0.02) (n = 6); hindtarsomere 2 dark-scaled proximally with basal dark band 0.29-0.52 length of tarsomere (mean = 0.43 ± 0.06) (n = 30).

Male: similar to An. albitarsis.

Male genitalia (Fig. 8): similar to An. albitarsis except as follow. Tubercle of parabasal spine 0.33-0.35 (mean = 0.34 ± 0.01) (n = 2) length of parabasal spine; dorsomedial rim 0.09-0.11 (mean = 0.10 ± 0.01) (n = 3) length of gonocoxite; dorsal accessory setae 0.33-0.41 (mean = 0.37 ± 0.04) (n = 3) length of gonocoxite; aedeagus 0.35-0.43 (mean = 0.39 ± 0.04) (n = 3) length of gonocoxite.

Pupa (Fig. 8): similar to An. albitarsis except as follows. Position and development of setae as figured; range and modal number of branches in Table VIII. All measurements were made on 10 specimens unless otherwise indicated. Abdomen: length 2.48-3.19 mm (mean = 2.69 ± 0.21); 5-I usually double, 6-I usually single, both 5,6-I long, 7-I with branches shorter than 6-I; 6-II single, 1.22-3.0 length of 7-II (mean = 2.22 ± 0.50) (n = 8), 9-II-IV less than 0.20 length of segment; 5-III with branches shorter than length of following segment, 9-III 1.42-3.90 (mean = 2.11 ± 0.70) length of 9-II; 10-III usually triple; 0-IV normally 4-branched, 9-IV 1.04-2.13 (mean = 1.67 ± 0.33) length of 9-III, 10-IV single or double, long; 3-V with branches extending beyond caudal margin of segment, 9-V 1.67-2.93 (mean = 2.19 ± 0.42) length of 9-IV, 9-V-VIII 0.32, 0.40, 0.51 and 0.44 length of segment, respectively, 10-V single, long; 0-VI,VII frequently 4-branched, 5-VI single or double, 9-VI, 1.14-1.80 (mean = 1.37 ± 0.21) length of 9-V; 5-VII always single, 9-VII 1.01-1.67 (mean = 1.25 ± 0.17) length of 9-VI; 9-VIII 0.78-1.08 (mean = 0.90 ± 0.08) length of 9-VII. Paddle 1.35-1.51 (mean = 1.42 ± 0.06) longer than wide, length 0.71-0.87 mm (mean = 0.77 ± 0.05), width 0.49-0.64 mm (mean = 0.54 ± 0.04), refractile index 0.70-0.77 (mean = 0.75 ± 0.02); seta 1-Pa stronger than 2-Pa, 2-Pa often double.

Fourth-instar larva (Fig. 9): similar to An. albitarsis except as follows. Position and development of setae as figured; range and modal number of branches in Table IX. Measurements were made on 10 specimens unless otherwise indicated. Head: length 0.68-0.73 mm (mean = 0.71 ± 0.02), width 0.60-0.64 mm (mean = 0.62 ± 0.01) (n = 9). Integument weakly pigmented with darker spots posteriorly on dorsal apotome and on lateralia; labiogula darkened along hypostomal suture and hypocranial ecdysial line. Antenna: length 0.31-0.34 mm (mean = 0.32 ± 0.01), enlarged toward base, 7.56-9.14 (mean = 8.12 ± 0.44) longer than wide; seta 1-A 0.25-0.35 (mean = 0.30 ± 0.04) distance from base. Seta 2-C 1.17-1.50 length of 3-C (mean = 1.31 ± 0.11), distance between bases 4.50-5.0 (mean = 4.75 ± 0.26) width base of single seta, 3-C 0.67-0.86 length of 2-C (mean = 0.77 ± 0.06), clypeal index 1.10-1.44 (mean = 1.23 ± 0.12). Thorax: setae 1, 2-P sometimes sharing a common tubercle, 1-P palmate with large pointed leaflets; 1-M strongly plumose; 3-T palmate with moderately long narrow leaflets. Abdomen: seta 1-I-VII palmate, 11-I triple, large, 13-I, III often triple; 0-II-VII large, 1-II-VII with dark, moderately narrow pointed leaflets; 2-IV single, 2-V long, single or double. Pecten with four or five long, 10-16 short spines, long spines 2.30-2.88 (mean = 2.53 ± 0.17) length of short spines; lateral arm of median plate of spiracular apparatus short to moderately long, directed dorsolaterally. Segment X: seta 1-X inserted inside saddle.

Distribution - An. oryzalimnetes n. sp. seems to be a widely distributed species in Brazil and Paraguay. In Brazil it is found in the states of Espírito Santo, SP, PA, PR, MT, Bahia, Ceará and Rio de Janeiro (RJ) (Wilkerson et al. 1995a, c, Lehr et al. 2005). In Paraguay, An. oryzalimnetes n. sp was found in Hernanderias and near the National Airport (Wilkerson et al. 1995c).

Material examined - Table I.

Type data - All individuals from the type series of this species and An. janconnae n. sp were obtained from link-reared offspring of females collected in a Shannon trap and later given a blood meal in the laboratory. The accession codes are as follows: the first two capital letters are the country code, followed by the collection number, the number between brackets specifies the field collected female and the last number denotes the specimen number. Specimen numbers > 100 indicate the adult is linked with a pupal exuviae, whereas numbers < 99 means indicate that the adult has associated larval and pupal exuviae. Holotype: adult male with associated with larval and pupal exuviae mounted on microscope slide: Brazil, SP, registro municipality, Centro de Desenvolvimento Agrícola do Vale do Ribeira (CEDAVAL) (24º36.8'S 47º53.1'W), 26 January 1992, Wilkerson and Klein coll., WRBU Acc. 1527, BR500(45)-9, deposited in the Entomological Collection of FSP-USP, accession E-12935. Allotype: adult female with associated larval and pupal exuviae mounted in microscope slide, with the same collection data of the holotype and from the same progeny, WRBU Acc. 1527, BR500(45)-12, deposited in the Entomological Collection of the National Museum of Natural History (NMNH), Smithsonian Institution. Paratypes: two hundred twenty-six adults male and female, collection code WRBU Acc. 1527, as follows: BR500(1), 11 adults male and female with associated larval and pupal exuviae mounted on microscope slides; BR500(18), eight adults with associated larval and pupal exuviae mounted on microscope slides; BR500(2), nine adults with associated larval and pupal exuviae mounted on microscope slides; BR500(35), 12 adults with associated larval and pupal exuviae mounted on microscope slides; BR500(37), 17 adults with associated larval and pupal exuviae mounted on microscope slides; BR500(4), 12 adults with associated larval and pupal exuviae mounted on microscope slides; BR500(44), 19 adults with associated larval and pupal exuviae mounted on microscope slides; BR500(45), 10 adults with associated larval and pupal exuviae mounted on microscope slides, six with pupal exuviae, four not associated with immature; BR500(46), 11 adults with associated larval and pupal exuviae mounted on microscope slides, 62 with pupal axuviae, four not associated with immature; BR500(5), 10 adults with associated LE and Pe mounted on microscope slides; BR500(6), eight adults with associated LE and Pe mounted on microscope slides; BR500(7), 11 adults with associated LE and Pe mounted on microscope slides; BR500(8), eight adults with associated LE and Pe mounted on microscope slides; BR500(9), 10 adults with associated LE and Pe mounted on microscope slides; BR500(1), eight adults with associated LE and Pe mounted on microscope slides; BR501(2), nine adults with associated LE and Pe mounted on microscope slides; BR501(34), nine adults with associated Le and Pe mounted on microscope slides, three with Pe, five not associated with immature; BR501(4), nine adults with associated LE and Pe mounted on microscope slides; BR501(5), nine adults with associated LE and Pe mounted on microscope slides. Paratypes are deposited in the Entomological Collection of the NMNH, FSP-USP and Natural History Museum, London, UK.

Bionomics - Because An. oryzalimnetes n. sp has been largely misidentified as An. albitarsis, An. deaneorum or An. marajoara, little is known about its bionomics and medical importance. Kakitani and Forattini (2000) (as An. albitarsis A) demonstrated that its daily survival rate was 0.5339 ± 0.047 and the duration of the gonotrophic cycle was 1.99 days. Also, An. oryzalimnetes n. sp. (as An. albitarsis A) was attracted to human bait and was common in rice fields and in surrounding dwellings in the Ribeira Valley, southeast of SP, Brazil. In the Ribeira Valley, An. albitarsis and An. oryzalimnetes n. sp. are sympatric. Also, in Paraguay An. albitarsis, An. oryzalemnetes and An. deaneorum were found to be sympatric (Wilkerson et al. 1995c). Furtermore, An. oryzalimnetes n. sp showed unimodal sunset crepuscular rhythms (Forattini et al. 1996). In another study carried out in the same region of the Ribeira Valley, Forattini et al. (1995) observed a concentration of An. albitarsis and An. oryzalimnetes n. sp. in rice field environments. An. oryzalimnetes n. sp. was also collected at sunset and sunrise on human bait captures performed indoors and outdoors in a rice plantation environment.

Medical importance - Nothing is known about medical importance of An. oryzalimnetes n. sp.

Molecular characterization - An. oryzalimnetes can be recognized by species-specific RAPD-PCR bands (Wilkerson et al. 1995a, c) generated with Operon primers C07, B02 and C15. Additionally, Li and Wilkerson (2005) developed species-specific ITS2 primers to separate An. oryzalimnetes from other species of the An. albitarsis complex. Lehr et al. (2005) and Wilkerson et al. (2005) using distinct molecular markers corroborated the monophyly of An. oryzalimnetes. Also, Merrit et al. (2005) and Brochero et al. (2007) using the white gene sequence data corroborated An. oryzalimnetes to be distinct from the other species of the An. albitarsis complex.

Anopheles (Nyssorhynchus) janconnae Wilkerson and Sallum, n. sp.

An. albitarsis species E of Lehr et al. 2005: 908-917 (tax., mtDNA); Póvoa et al. 2006: 163-168 (biology).

Etymology - we are pleased to honor Jan Conn, collaborator, respected scientist, poet and friend, for her outstanding contributions to the advancement of medical entomology, especially on population genetics and phylogeography of species of Anopheles (Nyssorhynchus).

Female: similar to An. albitarsis except as follows. Proboscis brown to dark brown, with decumbent scales and short setae, length 1.68-1.97 mm (mean = 1.78 ± 0.10) (n = 10), 1.27-1.43 length of forefemur (mean = 1.35 ± 0.06) (n = 10), 1.01-1.12 length of maxillary palpus (mean = 1.06 ± 0.03) (n = 10). Labella similar in color to labium. Palpus 1.62-1.83 mm (mean = 1.69 ± 0.07) (n = 10), 0.89-0.99 length of proboscis (mean = 0.94 ± 0.03) (n = 10); length palpomere 2/palpus length 0.25-0.30 (mean = 0.28 ± 0.01) (n = 10); length palpomere 3/palpus length 0.33-0.39 (mean = 0.36 ± 0.02) (n = 10); length palpomere 4/palpus length 0.16-0.21 (mean = 0.18 ± 0.01) (n = 10); length palpomere 5/palpus length 0.12-0.15 (mean = 0.14 ± 0.01) (n = 10). Wing: length 2.76-3.19 mm (mean = 2.91 ± 0.10) (n = 30); veins dark-scaled with spots of white scales on anterior area of costa, subcosta, R and R₁, pale yellow scales on remaining veins. Forefemur 1.26-1.40 mm (mean = 1.33 ± 0.05) (n = 10), 0.70-0.78 length of proboscis (mean = 0.73 ± 0.02) (n = 10); hindtarsomere 2 dark-scaled proximally with basal dark band 0.28-0.51 length of tarsomere (mean = 0.39 ± 0.06) (n = 30).

Male: similar to An. albitarsis.

Male genitalia (Fig. 10): similar to An. albitarsis except as follows. Tubercle of parabasal spine 0.22-0.35 (mean = 0.28 ± 0.05) (n = 3) length of parabasal spine; dorsomedial rim 0.11-0.12 (mean = 0.12 ± 0.01) (n = 2) length of gonocoxite; dorsal accessory setae 0.36-0.45 (mean = 0.39 ± 0.03) (n = 4) length of gonocoxite; aedeagus 0.43-0.47 (mean = 0.45 ± 0.01) (n = 4) length of gonocoxite.

Distribution - An. janconnae n. sp is known from Northern Brazil and Venezuela (Lehr et al. 2005).

Material examined -Table I.

Type data - Holotype: adult male with dissected male genitalia on microscope slide. Brazil, RR, Boa Vista municipality, (2º49'S 60º40'W), 2002, Wilkerson coll., WRBU BR24(9)-100, deposited in the FSP-USP collection, under Acc. E-12936. Paratypes: 1 MG (WRBU Acc. 1734, BR24(5)-100, FSP Acc. E-12946); 7 F (WRBU Acc. 1734, BR17-10, BR17-32, BR17-40, BR17-20, BR24(9)-101, BR11-107, BR17-1, deposited in the FSP-USP under the Acc. E-12947, E-12948, E-12949, E-12950, E-12951, E-12952, E-12953); 42 F (WRBU Acc. 1734, BR11-13, BR11-14, BR11-15, BR11-106, BR11-108, BR17-18, BR17-19, BR17-28, BR17-39, BR17-42, BR19-3, BR19-4, BR19-6, BR19-10, BR19-11, BR19-14, BR19-24, BR19-25, BR19-26, BR24(4)-1, BR24(9)-1, BR25-11, BR25-12, BR25-16, BR25-18, BR25-22, BR25-24, BR26-1, BR26-7, BR26-9, BR27-1, BR27-5, BR27-108, BR27-109, BR30-1, BR30-5, BR30-7, BR30-8, BR31-3, BR31-7, BR34-3, BR36- 103, deposited in NMNH, USA), 1M (WRBU Acc. 1734, BR23(4)-1, deposited in NMNH, 2MG (WRBU Acc. 1734, BR24(8)-100, BR24(9)-2, deposited in NMNH, same collection data as holotype.

Bionomics - Póvoa et al. (2006) observed that Anopheles janconnae n. sp. was the most abundant species collected in Boa Vista, RR. In this region this species is anthropophilic with peak biting activity usually occurring before midnight as was observed for An. marajoara in Western Venezuela (Rubio-Palis & Curtis 1992).

Medical importance - An. janconnae n. sp is an important malaria vector at least in the savannah biome around Boa Vista, RR. Specimens of An. janconnae were found infected with P. falciparum, P. vivax VK 210, P. vivax VK247 and P. malariae (Póvoa et al. 2006).

Molecular characterization - Genetic and phylogenetic evidence support the existence of An. janconae in Northern Brazil and Venezuela. Kreutzer et al. (1976) found three chromosomally differentiated populations with the "C" form found in Venezuela and Colombia. Also, it is possible that the "iii" group designated by Rosa-Freitas et al. (1990), based on allozyme data, correspond to An. janconnae n. sp. Support for An. janconnae n. sp. as a distinct species were also found in a phylogenetic analysis of the complete COI gene by Lehr et al. (2005). However, Wilkerson et al. (1995a, c) using RAPD-PCR profiles and Li & Wilkerson (2005) using ITS2 sequence found no evidence to support a distinct species within the An. albitarsis complex.

DISCUSSION

To name the two species described here we considered the possibility that a name currently in synonymy might already exist for these species. In synonymy with An. marajoara is An. domesticus Galvão and Damasceno, which was originally described as a subspecies of An. albitarsis, but later shown by Rios et al. (1984) to be indistinguishable from their concept of An. albitarsis. This nominal species was later synonymized with An. marajoara by Linthicum (1988). Given that there is no extant type and that its type locality is the same as for An. marajoara, we agree with Linthicum's (1988) assessment. Another name associated with An. marajoara is Anopheles allopha Peryassú. Because it has proven impossible to characterize and because the existing syntypes are actually Anopheles. argyritarsis, it was considered to be a nomen nudum by Lourenço-de-Oliveira and Deane (1984) and a nomen dubium by Linthicum (1988). An. imperfectus was described by Corrêa and Ramos (1943) as a variety of An. albitarsis, based on an adult female collected in municipality of Vera Cruz, SP. Accordingly, An. imperfectus was considered to be morphologically similar to An. albitarsis from which it could be distinguished by having a dark ring on the basal 0.3 of hindtarsomere 3 and no SC pale spot the costa. Lane (1953) transferred An. imperfectus to the synonymy of An. albitarsis, which was later accepted by Linthicum (1988). We examined the holotype and confirmed both the presence of a dark ring on the basal 0.3 of hindtarsomere 3 and the absence of a SC pale spot on the costa. Additionally, hindtarsomere 2 has dark scales on the basal 0.8 and pale scales on the apical 0.2. By comparing the holotype of An. imperfectus with species of An. albitarsis complex included in this study, we conclude that An. imperfectus should be remain in the synonymy with An. albitarsis since it has hindtarsomere 2 dark-scaled in the basal 0.8. Among members of the An. albitarsis complex, only An. deaneorum and An. albitarsis have hindtarsomere 2 dark in the basal 0.51-0.90 and 0.52-0.86, respectively. However, in An. deaneorum, hindtarsomere 1 has a conspicuous ring of white scales distally, whereas in An. albitarsis, hindtarsomere 1 is entirely dark. Similar to An. albitarsis, An. imperfectus has hindtarsomere 1 dark at apex. The presence of dark scales on the basal 0.3 of hindtarsomere 3 of the holotype of An. imperfectus may represent a variant of An. albitarsis. Similar variability also has been documented in An. darlingi (Harbach et al. 1993). Furthermore, Wilkerson et al. (1995b) demonstrated that in Anopheles rondoni the basal dark ring on hindtarsomere 3 may be present or absent, additionally it was proposed that in the subgenus Nyssorhynchus, individuals with a long dark band on hindtarsomere 2 were more likely to have a basal dark band on hindtarsomere 3.

An. limai was described as a variety of An. albitarsis by Galvão and Lane (1937a). Validation of An. limai was based on the eggs and adult female characteristics; however, no type was designated. In the Entomological Collection of FSP-USP there are three microscope slides with the midguts of females of An. albitarsis collected in Pinheiros and Butantan district, municipality of SP. These slides represent specimens employed by Galvão and Lane (1937b) in experimental malaria infection tests. There are no other remnants in the FSP-USP collection of these females or of the eggs used to characterize An. albitarsis var. limai. Considering that the only specimens available were not used for the validation of An. limai, we consider that no types exist to represent this species. Galvão and Lane (1937a) reported that females of An. limai could be distinguished from specimens of An. albitarsis of Root (1926) in having hindtarsomere 2 with a more extensive basal dark ring. The hindtarsomere illustrated by Root (1926; Pl. II) is dark in more than basal the 0.5. In considering that Galvão and Lane (1937a) described the basal dark area of hindtarsomere 2 of An. limai as more extensive than that of An. albitarsis shown by Root (1926), we concluded that An. limai was correctly transferred to synonymy with An. albitarsis. Furthermore, Linthicum (1988) examined individuals from the type locality of An. limai and concluded that this nominal species is conspecific with An. albitarsis. For the reasons mentioned above, An. limai and An. imperfectus are retained in synonymy with An. albitarsis. Since the species we treat here are distinct from known nominal species, they are described as An. oryzalimnetes n. sp. and An. janconnae n. sp.

Multivariate analysis of morphometric characters has been employed as a useful tool for separating sibling species of Anopheles (Nyssorhynchus). For example, Calle et al. (2002) discriminated adult females of Anopheles rangeli, Anopheles oswaldoi, Anopheles benarrochi, Anopheles triannulatus and Anopheles nuneztovari from Colombia. Similarly, Rubio-Palis et al. (1997) and Rubio-Palis (1998) separated adult females of An. darlingi, An. marajoara, Anopheles braziliensis and An. argyritarsis in Venezuela.

Despite of being polymorphic, the pattern of pale and dark wing spots is often employed for Anopheles species identification (Faran 1980, Linthicum 1988, Hribar 1995). Faran (1980) and Linthicum (1988) used the range and ratio of the length of several pale and dark wing spots to identify species of the Albimanus and Argyritarsis Sections of Anopheles (Nyssorhynchus), respectively. Later, Hribar (1995) used the length of the costal wing spots to separate individuals of An. nuneztovari from Brazil and Venezuela. To examine the utility of the wing spots to separate individuals of An. nuneztovari from other morphologically similar species, Ramos et al. (2008) examined individuals from three localities in Colombia to evaluate variation in the ratio of several wing spots used in adult female identification keys and found that 5% of the specimens could be misidentified as other species of the subgenus Nyssorhynchus.

Results of the statistical analyses carried out in the present study suggest that the specimens of An. marajoara collected in SP, PA, MT and AM, Brazil, and Zulia Department of Venezuela, which have identical RAPD-PCR profiles, belong to two distinct species. These results validate the hypothesis of Lehr et al. (2005) regarding the existence of an unidentified species, An. albitarsis E (= An. janconnae), in areas of savannah in RR and in Venezuela.

Merritt et al. (2005) found a reliable method based on a fragment of the nuclear white gene to distinguish An. marajoara from the other members of the An. albitarsis complex. A pronounced difference in size of the nuclear white locus fragment was due to the absence of intron IV in all species of the An. albitarsis complex, except An. marajoara. Consequently, Merrit et al. (2005) observed that a simple PCR of the white gene could separate An. marajoara by the visualization of the PCR product in a gel stained with ethidium bromide. However, when analyzing the same white gene fragment for a larger sample size, which included specimens from Colombia and also An. janconnae n. sp. (as An. albitarsis E), Brochero et al. (2007) observed that An. janconnae n. sp. (also as An. albitarsis E) clustered together with An. marajoara with strong bootstrap support. It is interesting that An. janconnae n. sp. also possess intron IV. Consequently, the presence of white gene intron IV separates An. marajoara and An. janconnae n. sp. from the other species of the An. albitarsis complex.

An. deaneorum is distinguished by the development of larval 3-C seta, which is branched in An. deaneorum (Rosa-Freitas 1989) and single in the other species. Furthermore, results of the statistical analyses carried out in the present study show that based on the ratio of the length of the basal dark portion of hindtarsomere 2 and hindtarsomere 2 length it is possible to distinguish two major groups. One group is formed by An. albitarsis (mean = 0.62) and An. deaneorum (mean = 0.67). In this group the ratio varied from 0.51-0.90. In contrast, in a second group composed of An. oryzalimnetes (mean = 0.42), An. marajoara (mean = 0.48) and An. janconnae (mean = 0.39), the ratio varied from 0.28-0.63. There is an overlap of this character, however, when using the extreme values it is possible to separate species into two groups with confidence. Additionally, some wing spots are useful for separating species of the An. albitarsis complex. For example, the length of the accessory sector pale spot can distinguish An. albitarsis and An. oryzalimnetes n. sp. For An. albitarsis, the accessory sector pale spot showed a higher mean value, whereas for An. oryzalimnetes n. sp. it showed a lower mean value (Fig. 1H). The mean value of the length of the subcostal pale spot is high for An. deaneorum. Consequently, it can be used to separate An. deaneorum from the others species (Fig. 1K). An. janconnae can be separated using both the 1st dark spot of vein CuA₁ and the humeral dark spot of the costa (Figs 1L, 1M). The mean values of these characters are higher in An. janconnae n.sp. than in the other species of the complex.

ACKNOWLEDGEMENTS

To two reviewers, for their great contribution to the improvment of the text, to Eduardo S Bergo, SUCEN, SP, and JB Lima, Fiocruz, RJ, for helping with mosquito collections in Brazil.

Received 22 January 2009

Accepted 22 June 2009

Financial support: FAPESP (05/53973-0 to MAMS), CNPq (472485/2006-7 to MAMS), NIH (AI RO154139 to JE Conn). MTM is a doctorate fellow from Fapesp (2007/07573-5).

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Publication Dates

• Publication in this collection
  30 Oct 2009
• Date of issue
  Sept 2009

History

• Accepted
  22 June 2009
• Received
  22 Jan 2009