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Fig. 1 in Susceptibility status to temephos in larval Aedes aegypti and Aedes albopictus (Diptera: Culicidae) populations from Quintana Roo, southeastern Mexico
Fig. 1. Susceptibility status to temephos (1× the discriminant dose) of Aedes albopictus (grey pie charts) and Aedes aegypti (black and white pie charts) larvae from 4 communities of Quintana Roo, Mexico.
Fig. 5 in Geomorphic morphometric differences between populations of Speyeria diana (Lepidoptera: Nymphalidae)
Fig. 5. Principal components analysis showing separation of male (red) and female (blue) Speyeria diana forewing shape. Male forewings (n = 166) were narrower and more angular than female forewings (n = 101), which were wider and more rounded.
Fig. 2 in Geomorphic morphometric differences between populations of Speyeria diana (Lepidoptera: Nymphalidae)
Fig. 2. Twenty-two vein intersections on the Speyeria wing were used as landmarks for this study based on Borror et al. 2005.
Fig. 1 in Geomorphic morphometric differences between populations of Speyeria diana (Lepidoptera: Nymphalidae)
Fig. 1. Female (lef) and male (right) Speyeria diana specimens were photographed for this study. All specimens were photographed with a cm ruler for proper scaling.
Fig. 6 in Geomorphic morphometric differences between populations of Speyeria diana (Lepidoptera: Nymphalidae)
Fig. 6. Principal components analysis showing separation of male Speyeria diana forewings from specimens collected from eastern (blue) and western (red) populations. Male hind wings from eastern populations (n = 131) were narrower than those from western populations (n = 102).
Fig. 5 in Phenotypic structure of Colombian populations of Anastrepha fraterculus complex (Diptera: Tephritidae)
Fig. 5. Box-plots of the significant linear variables and Kruskal-Wallis analysis of means comparing eggs among populations of the Anastrepha fraterculus Andean morphotype in Colombia. Means topped by the same letter are not significantly different at the 5% significance level.
Fig. 3 in Phenotypic structure of Colombian populations of Anastrepha fraterculus complex (Diptera: Tephritidae)
Fig. 3. Box-plots of the significant linear variables and Kruskal-Wallis analysis of means comparing males among populations of the Anastrepha fraterculus Andean morphotype in Colombia. Means topped by the same letter are not significantly different at the 5% significance level.
Fig. 4 in Phenotypic structure of Colombian populations of Anastrepha fraterculus complex (Diptera: Tephritidae)
Fig. 4. Box-plots of the significant linear variables and Kruskal-Wallis analysis of means comparing larvae among populations of the Anastrepha fraterculus Andean morphotype in Colombia. Means topped by the same letter are not significantly different at the 5% significance level.
Fig. 2 in Phenotypic structure of Colombian populations of Anastrepha fraterculus complex (Diptera: Tephritidae)
Fig. 2. Box-plots of the significant linear variables and Kruskal-Wallis analysis of means comparing females among populations of the Anastrepha fraterculus Andean morphotype in Colombia. Means topped by the same letter are not significantly different at the 5% significance level.
Fig. 1 in Phenotypic structure of Colombian populations of Anastrepha fraterculus complex (Diptera: Tephritidae)
Fig. 1. Geographic distribution of populations of the Anastrepha fraterculus Andean morphotype collected in Colombia. Chp: Cachipay; Dtm: Duitama; Flb: Florida Blanca; Ibg: Ibagué; Lun: La Unión; Pns: Pensilvania; Rnd: Roldanillo; Sby: Sibundoy; Svl: Sevilla.
Fig. 1 in Using hydrogen stable isotope ratios to trace the geographic origin of the population of Bactrocera dorsalis (Diptera: Tephritidae) trapped in northern China
Fig. 1. Implied relationship standard curve equation between Bactrocera dorsalis and precipitation based on a δ2H stable isotope (solid line indicates the linear regression and dash lines indicate the 95% confident intervals).
Fig. 1 in Potential of unmanned aerial sampling for monitoring insect populations in rice fields
Fig. 1. Rotary-wing unmanned aerial vehicle equipped with remote-controlled insect net openings (a). Layout of double-layered insect net designed to prevent loss of insect samples during aerial sampling (b). Representative flight path of unmanned aerial vehicle for aerial sampling over rice field (c).
Fig. 4 in Acaricide efficacy and resistance in South Carolina tomato populations of twospotted spider mite
Fig. 4. LC50 values (± 95% confidence interval) for 7 AIs screened against a known-susceptible lab colony and 3 field-collected populations of Tetranychus urticae. When present, the dashed line indicates the amount of AI in the maximum labelled field rate. This value also is indicated in each graph by "FR=". The resistance ratio of each AI × population is written above each data point.
Fig. 1 in Acaricide efficacy and resistance in South Carolina tomato populations of twospotted spider mite
Fig. 1. Mean (± SE) spider mite (Tetranychus urticae) counts per tomato leaflet in a 2015 and 2016 acaricide efficacy trial conducted in South Carolina, USA. Arrows indicate dates of acaricide applications. Treatments with the same letter within a date are not statistically different (lsmeans P> 0.05). "ns" indicates that the overall model was not significant. The dotted line represents the action threshold for spider mites in tomato (2 per leaflet).
Fig. 2 in Acaricide efficacy and resistance in South Carolina tomato populations of twospotted spider mite
Fig. 2. Mean (± SE) cumulative mite d of Tetranychus urticae in a 2015 and 2016 acaricide efficacy trial conducted in South Carolina, USA. Arrows indicate dates of acaricide applications. Treatments with the same letter within a date are not statistically different (lsmeans P> 0.05). "ns" indicates that the overall model was not significant.
Fig. 3 in Alien populations of painted frogs, genus Discoglossus, on the southeastern coast of France: two examples of anthropogenic introduction
Fig. 3. Maximum Likelihood tree of Discoglossus based on a 258 bp fragment of the mitochondrial cytochrome b gene. Numbers at nodes are bootstrap values (500 pseudoreplicates) in percent. After the locality, sample numbers are given, including GenBank accession numbers in parentheses for those sequences taken from GenBank. "Z" marks sequences from the work of Zangari et al. (2006). Samples from the two newly discovered introduced populations are highlighted in bold, red font.
Fig. 1 in Changing blow fly (Diptera: Calliphoridae) populations in Orlando, Florida, United States
Fig. 1. Summary of species and numbers of blow fly collected in 2009 (by aerial netting) and 2010 (by Bishopp cone trap). Only 5 species of calliphorids were recovered: Chrysomya rufifacies, Chrysomya megacephala, Cochliomyia macellaria, Lucilia coeruleiviridis, and Lucilia sericata.
Fig. 2 in Alien populations of painted frogs, genus Discoglossus, on the southeastern coast of France: two examples of anthropogenic introduction
Fig. 2. (A) Adult male Discoglossus sardus from Marseille, 31 May 2018. (B) Discoglossus sardus habitat in the city of Marseille. (C) Adult Discoglossus pictus from Grimaud, 7 November 2018. (D) Discoglossus pictus habitat in Grimaud. The white arrow indicates the position of a ditch filled with water, where three individuals were observed. Photos by Mathieu Policain (A–B), Julien Renet (C), and Google Map/Street View (D).
Fig. 1 in Alien populations of painted frogs, genus Discoglossus, on the southeastern coast of France: two examples of anthropogenic introduction
Fig. 1. (A) Map of the ranges of D. sardus (orange: native population range) and D. pictus (purple: original distribution range; pink: introduced population range). (B) Enlarged view of the area with the newly introduced populations of the two species in southern France (orange star: D. sardus in Marseille; pink square: D. pictus in Grimaud), which is indicated by the black rectangle in (A).
Fig. 6 in Discovery of a reproducing population of the Mindo Glassfrog, Nymphargus balionotus (Duellman, 1981), at the Río Manduriacu Reserve, Ecuador, with a literature review and comments on its natural history, distribution, and conservation status
Fig. 6. Nymphargus balionotus breeding behavior. (A) Calling male; (B) Male and female in amplexus; (C) Egg mass deposited on the bottom surface on a leaf. Photos by Ross J. Maynard (A) and Jaime Culebras (B–C).
ScienceDex guides
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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.