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256 results for “Aedes aegypti”
Fig. 1 in Effect of erythritol and sucralose formulation on the survivorship of the mosquito Aedes aegypti
Fig. 1. Survivorship of Ades aegypti afer consumption of erythritol formulations: E + S (1.5 M erythritol + 0.5 M sucrose), E + Sul (1.5 M erythritol + 0.1 M sucralose), Sucrose (0.5 M sucrose) as a positive control, and Water as a negative control for 7 d. Different letters denote (*P <0.05) differences by Tukey HSD test.
Figure 1 in Isolation of 4-nerolidylcatechol from leaves of Piper peltatum L., and evaluation of larvicidal activity in mosquito vectors, with emphasis on Aedes aegypti (Diptera: Culicidae)
Figure 1 Molecular chemical structure of the substances 4-nerolidylcatechol (4-NC), isolated of Piper peltata, and catechol and nerolidol were obtained from Sigma-Aldrich®, used in larvicidal and cytotoxicity bioassays.
Figure 3 in Isolation of 4-nerolidylcatechol from leaves of Piper peltatum L., and evaluation of larvicidal activity in mosquito vectors, with emphasis on Aedes aegypti (Diptera: Culicidae)
Figure 3 Frequency of anomalies in interphase nuclei. a – damage to Aedes aegypti neuroblasts exposed to 4-NC for two generations. b – data on Ae. aegypti oocytes exposed to 4-NC in G1.
Figure 2 in Isolation of 4-nerolidylcatechol from leaves of Piper peltatum L., and evaluation of larvicidal activity in mosquito vectors, with emphasis on Aedes aegypti (Diptera: Culicidae)
Figure 2 Microphotographs of abnormalities in interphasic and metaphasic nuclei of neuroblasts and oocytes of Aedes aegypti, stained with Giemsa (pH 5.8) and lacto-acetic orcein (2%). Arrows indicate: a – normal interphasic nuclei of neuroblasts of the NC group, G 1; b and c – micronuclei in interphasic nuclei of neuroblasts of G 2 (40 and 60 µg/mL), respectively; d – budding and telophasic bridging nucleus of neuroblasts (60 µg/mL, G2); e – budding in interphasic nucleus of oocytes (40 µg/mL, G1); f – normal metaphasic chromosomes (NC, G1); g and h – chromosomal metaphases of neuroblasts showing achromatic secondary constriction (60 µg/mL, G2). Magnification: 1600×. Scale bar: 5 and 10 µm.
Processed snRNAseq data from female Aedes aegypti antennal neurons
<p>Single-nucleus RNA sequencing data accompanying Adavi et al. 2024 <em>bioRxiv </em>preprint: https://doi.org/10.1101/2024.08.21.608847</p> <p>For analysis scripts see: https://github.com/mcbridelab/Adavi_2024_snRNAseqAaegAntennae</p> <p>For raw sequencing files see NCBI BioProject: PRJNA1138769</p>
Fig. 1 in Comparison of modified CDC gravid, BG-Bowl, and CDC autocidal gravid ovitraps to collect gravid and host-seeking Aedes aegypti (Diptera: Culicidae) in northeastern Florida
Fig. 1. Mean dissected female mosquitoes with non-gravid and gravid Ae. aegypti collected by 3 modified commercial mosquito traps afer release in screened outdoor enclosures.
Pairwise FST values for Aedes aegypti populations in Florida and southern California
<p>In the affiliated paper we compare likely the oldest populations of <i>Aedes aegypti</i> in continental North America with some of the newest to illuminate the range of genetic diversity and structure that can be found within the invasive range of this important disease vector. <i>Aedes aegypti</i> populations in Florida have likely persisted since the 1600-1700s, while populations in southern California derive from new invasions that occurred in the last ten years. For this comparison, we genotyped 1,193 individuals from 29 sites at 12 highly variable microsatellites and a subset of these individuals at 23,961 single nucleotide polymorphisms (SNPs). This dataset contains the pairwise FST values generated with both genetic datasets.</p>
SNP Data for Aedes aegypti populations in Florida and southern California
<p>In the affiliated paper we compare likely the oldest populations of <i>Aedes aegypti</i> in continental North America with some of the newest to illuminate the range of genetic diversity and structure that can be found within the invasive range of this important disease vector. <i>Aedes aegypti</i> populations in Florida have likely persisted since the 1600-1700s, while populations in southern California derive from new invasions that occurred in the last ten years. For this comparison, we genotyped 1,193 individuals from 29 sites at 12 highly variable microsatellites and a subset of these individuals at 23,961 single nucleotide polymorphisms (SNPs). This dataset contains the SNP genetic information.</p>
Microsatellite data for Aedes aegypti populations in Florida and southern California
<p>In the affiliated paper we compare likely the oldest populations of <i>Aedes aegypti</i> in continental North America with some of the newest to illuminate the range of genetic diversity and structure that can be found within the invasive range of this important disease vector. <i>Aedes aegypti</i> populations in Florida have likely persisted since the 1600-1700s, while populations in southern California derive from new invasions that occurred in the last ten years. For this comparison, we genotyped 1,193 individuals from 29 sites at 12 highly variable microsatellites and a subset of these individuals at 23,961 single nucleotide polymorphisms (SNPs).</p>
Figure 5 Nav kdr 1016 and 1534 in Genetic study in Aedes (Stegomyia) aegypti (Linnaeus, 1762) from Londrina (Paraná State, Brazil): an approach to population structure and pyrethroid resistance
Figure 5 Nav kdr 1016 and 1534 site allele frequencies in UEL. Collection site locations were distributed in the three regions of the campus.
Figure 4 in Genetic study in Aedes (Stegomyia) aegypti (Linnaeus, 1762) from Londrina (Paraná State, Brazil): an approach to population structure and pyrethroid resistance
Figure 4 Allele frequencies of Nav kdr 1016 and 1534 genotyping distributed in the five different regions of Londrina.
Figure 3 in Genetic study in Aedes (Stegomyia) aegypti (Linnaeus, 1762) from Londrina (Paraná State, Brazil): an approach to population structure and pyrethroid resistance
Figure 3 Haplotypic network obtained through specimens collected in UEL. The circles are proportional to the number of specimens observed in each haplotype.
Figure 2 in Genetic study in Aedes (Stegomyia) aegypti (Linnaeus, 1762) from Londrina (Paraná State, Brazil): an approach to population structure and pyrethroid resistance
Figure 2 Haplotype network observed in five regions of Londrina. The circles are proportional to the number of specimens observed in each haplotype. The haplotypes observed are in bold. The numbers represent nucleotide change positions.
Figure 1 in Genetic study in Aedes (Stegomyia) aegypti (Linnaeus, 1762) from Londrina (Paraná State, Brazil): an approach to population structure and pyrethroid resistance
Figure 1 Collection sites in Londrina. The red line is a boundary between the five regions of the city. The yellow ones represent the streets and avenues of the city. Only the urban area was evaluated in the study.
Fig. 1 in Isolation and molecular characterization of Bacillus thuringiensis found in soils of the Cerrado region of Brazil, and their toxicity to Aedes aegypti larvae
Fig. 1. SDS-PAGE protein profiles of the Bacillus thuringiensis isolates most toxic to Aedes aegypti larvae. MM, molecular weight marker (kDa); Bti, Bacillus thuringiensis var. israelensis; 25–560, Bacillus thuringiensis isolates.
Figure 3 in Isolation of Bacillus thuricgiecsis from tce state of Amazonas, in Brazil, and screening against Aedes aegypti %Diptera, Culicidae)
Figure 3. Amplification products of gen cry11Ba of dipteran-specific genes isolated from Bacillus thuringiensis from the state of Amazonas, Brazil. Legend: MM: marker 1kb-sized DNA ladder; 03: IBt-03; 06: IBt-06; 07: IBt-07; 28: IBt-28; 30: IBt-30; 27: BtAM-27; 82: Bti IPS-82 (positive control); NC: negative control.
Figure 2 in Isolation of Bacillus thuricgiecsis from tce state of Amazonas, in Brazil, and screening against Aedes aegypti %Diptera, Culicidae)
Figure 2. Amplification products of gen (A) cry10Aa and (B) cry11A of dipteran-specific genes isolated from Bacillus thuringiensis from the state of Amazonas, Brazil.
Figure 2 in Aedes aegypti queenslandensis: first geographic occurrence in Brazil and epidemiological implications
Figure 2 Comparative table between females of Aedes aegypti aegypti and Ae. aegypti queenslandensis.
Figure 2 in Mosquito Surveillance Program Using Ovitraps Detected Aedes aegypti at the Honolulu International Airport in 2012
Figure 2. Mean number of eggs collected monthly using ovitraps from Honolulu International Airport from May 2010 to June 2012. Monthly values are the averages of collections for all weeks in the month, by collection site.
Figure 1 in Mosquito Surveillance Program Using Ovitraps Detected Aedes aegypti at the Honolulu International Airport in 2012
Figure 1. Map of the Hawaiian Islands. Markers of "X" represent each of this study's Aedes aegypti collection sites on Oahu and Hawaii islands.
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