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1,024 results for “Mosquito”
Fig. 3 in Detection and molecular characterization of the mosquito-borne filarial nematode Setaria tundra in Danish roe deer (Capreolus capreolus)
Fig. 3. Neighbor-Joining phylogenetic relationship of four isolates of Setaria tundra from distant localities in Denmark. The analysis was based on cox1 gene sequences (578 bp). Percentage bootstrap support from 1000 replicate samples is indicated at the right of the supported node. Accession numbers for sequences obtained from GenBank are given in parentheses, followed by origin of isolate, only applicable to S. tundra. The scale bar indicates distance.
Fig. 1 in Detection and molecular characterization of the mosquito-borne filarial nematode Setaria tundra in Danish roe deer (Capreolus capreolus)
Fig. 1. Geographical origin (black dots) of Setaria tundra recovered from six infected roe deer. A: October 2010, B: May 2011, C: December 2012, D: May 2013 (two cases), and E: March 2014.
Fig. 2 in Detection and molecular characterization of the mosquito-borne filarial nematode Setaria tundra in Danish roe deer (Capreolus capreolus)
Fig. 2. Morphology of adult worms of Setaria tundra (A‾C) and microfilaria (D and E) recovered from roe deer in Denmark. A: Cephalic region showing the bifid projections (bp) carried on top of a peribuccal crown (pc) and one of the four cephalic papillae (cp). B: Posterior end of male worm with papillae weakly visible (arrowheads). C: Posterior end of female worm showing a knob at the tip of the tail (arrow head), that possesses longitudinal grooves and pores, a papilla (pa), and a collar composed of a row of bosses (co). D: Microfilaria collected from a female worm. The length of the microfilaria including the sheath (white arrow heads) was approximately 316 Mm, whereas the microfilaria was approximately 287 Mm, with a blunt anterior end and a tapering posterior end. E: Setaria tundra coiled under the liver capsule (case 3). Scale bars indicated for all but figure E.
Dataset for multiple blood feeding bouts in mosquitoes
<p>Dataset to accompany R code and findings in the Holmes et al., 2024 publication entitled, "Multiple blood feeding bouts in mosquitoes allow for prolonged survival and are predicted to increase viral transmission during dry periods."</p>
Novel Chromobacterium sp. isolated from mosquitos in Burkina Faso, West Africa
<p>Nov. <em>Chrombacterium</em> sp. isolated in wild caught mosquitos in Burkina Faso, West Africa </p>
Fig. 3 in Diversity Of Mosquitoes (Diptera, Culicidae) And Physico-Chemical Characterization Of Their Larval Habitats In Tizi-Ouzou Area, Algeria
Fig. 3. Mosquito breeding sites (site 01, a; site 02, b; site 03, c; site 04, d; site 05, e; site 06, f); site 07, g).
Evolution of a mosquito's hatching behavior to match its human-provided habitat
<p>A subspecies of the yellow fever mosquito, <em>Aedes aegypti</em>, has recently evolved to specialize in biting and living alongside humans. It prefers human odor and breeds in human-provided artificial containers rather than the forest tree holes of its ancestors. Here, we report one way this human specialist has adapted to the distinct ecology of human environments. While eggs of the ancestral subspecies rarely hatch in pure water, those of the derived human-specialist do so readily. We trace this novel behavior to a shift in how eggs respond to dissolved oxygen, low levels of which may signal food abundance. Moreover, we show that while tree holes are consistently low in dissolved oxygen, artificial containers often have much higher levels. There is thus a concordance between the hatching behavior of each subspecies and the aquatic habitat it uses in the wild. We find this behavioral variation is heritable, with both maternal and zygotic effects. The zygotic effect depends on dissolved oxygen concentration (i.e., GxE), pointing to potential changes in oxygen-sensitive circuits. Together, our results suggest that a shift in hatching response contributed to the pernicious success of this human-specialist mosquito and illustrate how animals may rapidly adapt to human-driven changes in the environment.</p>
Mosquito Tagging Using DNA-Barcoded Nanoporous Protein Microcrystals
<p>Contains raw data for the publication titled 'Mosquito Tagging Using DNA Barcoded Nanoporous Protein Microcrystals'.</p>
Carbon dioxide and blood-feeding shift visual cue tracking during navigation in Aedes aegypti mosquitoes
<p>Hematophagous mosquitoes need a blood meal to complete their reproductive cycle. To accomplish this, female mosquitoes seek vertebrate hosts, land on them, and bite. As their eggs mature, they shift attention away from hosts and towards finding sites to lay eggs. We asked whether females were more tuned to visual cues when a host-related signal, carbon dioxide, was present, and further examined the effect of a blood meal, which shifts behavior to ovipositing. Using a custom, tethered-flight arena that records wing stroke changes while displaying visual cues, we found the presence of CO2 enhances visual attention towards discrete stimuli and improves contrast sensitivity for host-seeking <em>Aedes aegypti</em> mosquitoes. Conversely, intake of a blood meal reverses vertical bar tracking, a stimulus that non-fed females readily follow. This switch in behavior suggests that physiological status modulates visual attention in mosquitoes, a phenomenon that has been described before in olfaction but not in visually-driven behaviors.</p>
Data from: Worldwide impacts of landscape anthropization on mosquito abundance and diversity: a meta-analysis
<p><span>In recent decades, the emergence and resurgence of vector-borne diseases have been well documented </span><span>worldwide</span><span>, especially in tropical regions where protection and defence tools for human populations are still very limited. In this context, the </span><span>dynamics</span><span> of pathogens </span><span>are influenced by</span><span> landscape anthropization (i.e., urbanization, deforestation, and agricultural development)</span><span>,</span><span> and one of the mechanisms through which this occurs is a change in</span><span> the</span><span> abundance and/or diversity of the vectors. An increasing number of empirical studies </span><span>have </span><span>described heterogeneous effects of landscape anthropization on vector communities</span><span>; therefore</span><span>, it is difficult to have an overall picture of these effects on a global scale. Here, we performed a meta-analysis to quantify the impacts of landscape anthropization on a global scale on the presence/abundance and diversity of mosquitoes, the most important arthropods affecting human health. We obtained 338 effect sizes on 132 mosquito species, compiled from 107 studies in 52 countries </span><span>that</span><span> covered almost every part of the world. The results of the meta-analysis showed an overall decline of mosquito presence/abundance and diversity in response to urbanization, deforestation, and </span><span>agricultural</span><span> development, except for a few mosquito species</span><span> </span><span>that have been able to exploit landscape anthropization well. Our results highlighted that these few favoured mosquito species are those of global</span><span> concern. </span><span>They thus provide a better understanding of the overall effect of landscape anthropization on vector communities and</span><span>,</span><span> more importantly, suggest a greater risk of emergence and transmission of vector-borne diseases in human-modified landscapes.</span></p>
Fig. 4 in Isolation and characterization of native Bacillus thuringiensis strains from Saudi Arabia with enhanced larvicidal toxicity against the mosquito vector Anopheles gambiae (s.l.)
Fig. 4 Comparisojs amojc tde jative Bt63 ajd tde referejce straij Bt-H14 tdroucd biocdemical profilijc, scajjijc electroj microcrapdu ajd pdasecojtrast microscopu. Ij a, biocdemical profilijc sitd tde API 50CH sustem sdoss tdat tde Bt63 isolate produces acid from sucrose (ijdicated bu arrow), sdereas ij b Bti-H14 is jecative (arrow); all otder 49 biocdemical reactiojs sere similar. Ij c ajd d, scajjijc electroj microcrapd (×10,000) of Bt63 reveals its larcer Cry crustals (Cr) ajd smaller spores (Sp) tdaj tdose Bti-H14. Ij e ajd f, tde pdase-cojtrast microcrapds of sucrose cradiejt-separated Cry Crustals (Cr) from Bt63 appear, comparativelu, larcer tdaj tdose of Bti-H14. Scale-bars: c, d, 1 μm; e, f, 10 μm
Fig. 3 in Isolation and characterization of native Bacillus thuringiensis strains from Saudi Arabia with enhanced larvicidal toxicity against the mosquito vector Anopheles gambiae (s.l.)
Fig. 3 SDS-PAGE profiles of sdole parasporal crustals/spores mixtures. a Profiles after dissolutioj of proteij crustals at alkalije pH (10.5–11). b Profiles follosijc pH-jeutralizatioj. c Profiles after trupsij-treatmejt (silver staij). Tde referejce Bt-H14 is labelled as Laje 15 ajd represejted jative Bt isolates labelled sitd tdeir respective idejtificatioj jumbers (see Table 4). Lajes M: proteij molecular mass markers (245 to 11 kDa). Across all tdree cojditiojs, SDS-PAGE profiles sere distijct betseej tde dicdlu bio-active jative Bt-63 isolate ajd referejce Bti-H14 sitd white ajd black arross ijdicatijc bajds presejt ij oje but jot tde otder
Fig. 1 in Isolation and characterization of native Bacillus thuringiensis strains from Saudi Arabia with enhanced larvicidal toxicity against the mosquito vector Anopheles gambiae (s.l.)
Fig. 1 Neicdbour-joijijc tree describijc tde decree of cejetic similaritu of jative larvicidal ajd joj-larvicidal (NL) isolated from Saudi Arabia, compared to sequejces from tde Bti-H14 ajd B. cereus referejce straij. Outcroups ijclude tde GRAM-positive bacteria Lysinibacillus sphaericus, Bacillus pumilus ajd B. megatorium. Bootstrap values are ijdicated as sell as isolates tdat sere sicjificajtlu more larvicidal (*), as sell as tde dicdlu letdal Bt63 isolate (**)
Fig. 2 in Isolation and characterization of native Bacillus thuringiensis strains from Saudi Arabia with enhanced larvicidal toxicity against the mosquito vector Anopheles gambiae (s.l.)
Fig. 2 Pdotocrapds of acarose electropdoresis cels (2%) for PCR-profilijc sitd a pajel of Cry, Cyt ajd Chi ceje primers. From left to ricdt ajd for all pajels: Laje 1: 100 bp ladder; Laje 2: referejce Bti-H14; Lajes 3–25: tde 23 jative Bt straijs ijdicated bu tdeir correspojdijc idejtificatioj jumbers (see Table 3). Ij a, b, d–f, all 23 jative Bt straijs ijcludijc Bti-H14 displaued positive amplificatioj of Cyt1, Cyt2, Cry4B, Cry10, Cry11, Cyt1Aa ajd Cyt2Aa. Ij c, all straijs sere positive for Cry4A except Bt63. Ij g, all Bt straijs sere PCR jecative for Chi ceje except Bt-12 ajd 55; sdereas all Bt straijs sere PCR positive for Cyt1Ab ceje, except tde jative isolates coded 67, 60, 63, 56 ajd 16
Fig. 1 in Description of an integrated management system for invasive mosquitoes at entry-exit ports in Zhejiang, China
Fig. 1 Framework of integrated management system for invasive mosquitoes at Zhejiang ports, China. Abbreviation: HC, Hangzhou Customs
Fig. 4 in Description of an integrated management system for invasive mosquitoes at entry-exit ports in Zhejiang, China
Fig. 4 Tools for online classification and taxonomy of mosquito identification keys using Lucid on the front-page internet (http://www.livefarm.cn/ lucid/mosquito)
Fig. 5 in Description of an integrated management system for invasive mosquitoes at entry-exit ports in Zhejiang, China
Fig. 5 Related supplemental information on exotic mosquitoes obtained from the identification keys on the front-page internet
Fig. 3 in Description of an integrated management system for invasive mosquitoes at entry-exit ports in Zhejiang, China
Fig. 3 Annual trends and species abundance of captured mosquitoes from 2011 to 2017 in the Zhejiang Province, China. a Dynamic variation of captured invasive mosquitoes. b Pie chart of mosquito species composition
Fig. 2 in Description of an integrated management system for invasive mosquitoes at entry-exit ports in Zhejiang, China
Fig. 2 Geographical distribution of surveillance points in Zhejiang Province, China (obtained from the National Platform for Common Geospatial Information Services)
Fig. 1 Mosquito collections 2011–2019 in Nine years of mosquito monitoring in Germany, 2011-2019, with an updated inventory of German culicid species
Fig. 1 Mosquito collections 2011–2019 (green dots—trap collections; red dots— 'Mueckenatlas' submissions; blue dots—netting, aspirating and baited collections of adults; yellow dots—dipping/sieving of immature developmental stages)
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.