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FIGURE 11 in Literature review of the systematics, biology and role in malaria transmission of species in the Afrotropical Anopheles subgenus Anopheles (Diptera: Culicidae)
FIGURE 11. Anopheles concolor: a, wing; b, palpomere; c, hindleg (from Gillies & de Meillon 1968).
FIGURE 3 in Literature review of the systematics, biology and role in malaria transmission of species in the Afrotropical Anopheles subgenus Anopheles (Diptera: Culicidae)
FIGURE 3. Anopheles coustani: a, wing; b, palpomere; c, hindleg (from Gillies & de Meillon 1968).
FIGURE 6 in Literature review of the systematics, biology and role in malaria transmission of species in the Afrotropical Anopheles subgenus Anopheles (Diptera: Culicidae)
FIGURE 6. Anopheles obscurus: a, wing; b, palpomere; c, hindleg showing variation (from Gillies & de Meillon 1968; Gillies & Coetzee 1987).
FIGURE 4 in Literature review of the systematics, biology and role in malaria transmission of species in the Afrotropical Anopheles subgenus Anopheles (Diptera: Culicidae)
FIGURE 4. Anopheles fuscicolor: a, wing; b, palpomere; c, hindleg (a and c from de Meillon 1947; b from Grjebine 1966).
FIGURE 1 in Literature review of the systematics, biology and role in malaria transmission of species in the Afrotropical Anopheles subgenus Anopheles (Diptera: Culicidae)
FIGURE 1. Wing of Anopheles female showing vein nomenclature (after Sallum et al. 2020). A, anal, CuA, anterior cubitus; M, media; R, radius.
Anopheles plumbeus decontaminated gx
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Comparative mitochondrial genome and phylogenetic analysis of malaria mosquitoes Anopheles hyrcanus and Anopheles messeae supplementary files
<p><strong>T</strong><strong><span>able</span></strong><strong> S1.</strong> This study encompassed 105 species, along with their corresponding taxonomy and GenBank registration numbers.</p> <p><strong>Figure S1</strong> Inferred secondary structures of tRNAs in the mt genome of <em>An. </em><em><span>h</span></em><em>yrcanus</em><em> </em><span>(A)</span><em> </em><span>and </span><em>An. </em><em><span>m</span></em><em>esseae</em><em> </em><span>(B)</span>, with corresponding amino acids labeled next to the tRNAs.</p>
Interrogation of the Seasonal Microbiome of Anopheles coluzzii in Mali
<p>These are the raw sequencing files (fastq) and scripts necessary to perform our analysis of the seasonal microbiome of <em>An. coluzzii </em>in Mali.</p>
Data from: Performance of five food regimes on Anopheles gambiae senso stricto larval rearing to adult emergence in Insectary
Background: Rearing of Anopheles gambiae s.s mosquitoes in insectary with quality cheap food sources is of paramount importance for better and healthy colony. This study evaluated larval survival and the development rate of aquatic stages of An.gambiae s.s under five food regimes; tetramin fish food (a standard insectary larval food), maize pollen, Cerelac, green filamentous algae and dry powdered filamentous algae. Methods: Food materials were obtained from different sources, cerelac was made locally, fresh filamentous algae was taken from water bodies, dry filamentous algae was ground to powder after it was dried under shade, and maize pollen was collected from the flowering maize. Each food source type was used to feed three densities of mosquito larvae 20, 60, and 100 in six replicates each. Larval age structure was monitored daily until pupation and subsequently adult emergence. Tetramin was used and taken as a standard food source for An. gambiae s.s. larvae feeding in Insectary. Results: Larval survivorship using maize pollen and Tetramin fish food was statistically insignificant (P = 0.564). However when compared to other food regime survivorship was significantly different with Tetramin fish food performing better than cerelac (P<0.001), dry algae (P<0.001) and fresh algae (P<0.001). The pupation rates and sex ratio of emerging adults had significant differences among the food regimes. Conclusion: The findings of this study have shown that maize pollen had closely similar nutritional value for larval survivorship to tetramin fish food, a standard larvae food in insectary. Further studies are required to assess the effect of food sources on various life traits of the emerged adults.
FIGURE 2 in A newly recognized species in the Anopheles Hyrcanus Group and molecular identification of related species from the Republic of South Korea (Diptera: Culicidae)
FIGURE 2. Results of amplification of rDNA ITS2 of An. sinensis (lane, progeny brood number): (1) KS8(67), (2) KS8(94); An. lesteri: (3) KS8(59), (4) KS8(88); An. pullus: (5) KS8(76), (6) KS8(86); An. unknown 1: (7) KS8(12), (8) KS7(27); An. unknown 2: (9) KS26(2) and (10) KS4 2(1); (11) positive control, complete ITS2 amplicon of KS8(67), An. sinensis; (12) negative control, no template. M: DNA ladder consisting of lambda DNA digested by Hind III, and phiX174 DNA digested with Hae III (Sigma, St. Louis, MO).
FIGURE 1. Ribosomal DNA ITS2 in A newly recognized species in the Anopheles Hyrcanus Group and molecular identification of related species from the Republic of South Korea (Diptera: Culicidae)
FIGURE 1. Ribosomal DNA ITS2 sequence for five Anopheles Hyrcanus Group species from the Republic of South Korea. Bases in the gray areas are common to all species. Speciesspecific primers and direction of amplification are indicated by arrows: sin = An. sinensis, unk1 = An. unknown 1, pul = An. pullus, unk2 = An. unknown 2, les = An. lesteri. Two numbers are given at the end of the figure: 1) ITS2 length, and 2) total length of amplified fragment, which includes 135 bases from the flanking regions.
FIGURE 1. Ribosomal DNA ITS2 in Molecular confirmation of Anopheles (Anopheles) lesteri from the Republic of South Korea and its genetic identity with An. (Ano.) anthropophagus from China (Diptera: Culicidae)
FIGURE 1. Ribosomal DNA ITS2 sequence for potential malaria vectors belonging to Anopheles (Anopheles) Hyrcanus Group from Korea, China, Japan and the Philippines. See Table 2 and text for sequence summaries and discussion. The following GenBank accession numbers correspond to the label numbers at the 5' end of the sequence: 1) AY375464; 2) AY375465; 3) AJ004942; 4) AY375466; 5) AF384172, AJ004941 and AF543860; 6) AY375467; 7) AY187728; 8) AY375468; 9) AY375469; 10) AY375470; 11) AY375471. The number of individuals sequenced, of those presented here for the first time, appears in parentheses
Anopheles plumbeus SPAdes preassembly
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FIGURE 2. a, b in The identity of Anopheles (Anopheles) barbirostris species A3 of the Barbirostris Complex (Diptera: Culicidae)
FIGURE 2. a, b, Wings of (a) An. hodgkini female with three apical fringe spots (arrow) and (b) An. dissidens with two apical fringe spots, without pale fringe spot at tip of vein R2 (arrow). c, d, Abdominal sterna of (c) An. hodgkini female with one pale and (d) An. dissidens female with two short lines of pale scales on sterna III and IV (arrows).
FIGURE 1. a, b in The identity of Anopheles (Anopheles) barbirostris species A3 of the Barbirostris Complex (Diptera: Culicidae)
FIGURE 1. a, b, Pupal trumpets of (a) An. hodgkini male showing the absence of a secondary cleft (arrow) and (b) An. dissidens showing the secondary cleft (arrow). c, d, Pupal seta 9-VII of (c) An. hodgkini, darkly pigmented, and (d) An. dissidens, lightly pigmented. e, f, Larval palmate seta 1–II of (e) An. hodgkini, unpigmented, and (f) An. dissidens, pigmented.
FIGURE 3 in The identity of Anopheles (Anopheles) barbirostris species A3 of the Barbirostris Complex (Diptera: Culicidae)
FIGURE 3. Maximum Likelihood tree of ITS2 sequences from specimens of An. barbirostris species A3 and other species of the Barbirostris Subgroup (which includes the Barbirostris Complex), with An. (Ano.) barbumbrosus Strickland & Chowdhury, 1927 and An. (Ano.) pullus Yamada, 1937 as outgroup taxa. Bootstrap values are shown at each node. All ambiguous positions were removed for each sequence pair (pairwise deletion option). The final dataset included 1,913 positions. The best-fit model was GTR+G. Evolution analyses were conducted in MEGA11.
Data from: Whole genome sequencing reveals absence of recent gene-flow and separate demographic histories for Anopheles punctulatus mosquitoes in Papua New Guinea
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Data from: Geographic population structure of the African malaria vector Anopheles gambiae suggests a role for the forest-savannah biome transition as a barrier to gene flow
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Data from: Laboratory rearing of Anopheles arabiensis: impact on genetic variability and implications for Sterile Insect Technique (SIT) based mosquito control in northern Sudan
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Data from: Extensive genetic diversity among populations of the malaria mosquito Anopheles moucheti revealed by population genomics
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