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Fig. 2. Statistical parsimony cladogram network representing relationships among the 45 haplotypes for a 615 in Genetic diversity of Halyomorpha halys (Hemiptera, Pentatomidae) in Korea and comparison with COI sequence datasets from East Asia, Europe, and North America
Fig. 2. Statistical parsimony cladogram network representing relationships among the 45 haplotypes for a 615 bp fragment of the COI gene of Halyomorpha halys. Each circle is labeled with haplotype number, and the size of each circle is proportional to the frequency of each haplotype [H3 (n = 353); H1 (n = 285); H22 (n = 43); H8 (n = 34); H33 (n = 23); H2 (n = 16); H32 (n = 8); H7, H9–H13, and H43 (n = 3); H6, H14, H34, H39, and H40 (n = 2); H4–H5, H12, H15–H21, H23, H30–H31, H35–H38, H41, H42, and H44–H51 (n = 1)]. Differing colors indicate countries in which samples were collected.
Fig. 2 in Impacts of a highway on the population genetic structure of a threatened freshwater turtle (Glyptemys insculpta)
Fig. 2. Estimate of short-term gene flow among populations north and south of Interstate Highway 88 (gray bar) and the Susquehanna River (dashed line) shown with 95% confidence intervals. Circle size reflects relative sample size. Values inside of circles represent the contribution of gene flow from within populations.
Fig. 1. Study area. Interstate Highway 88 in Impacts of a highway on the population genetic structure of a threatened freshwater turtle (Glyptemys insculpta)
Fig. 1. Study area. Interstate Highway 88 (I-88) and the Susquehanna River (Susq.) bisect Otsego and Delaware Counties, New York, USA.
Fig. 1 in Revision of the genus Thinophilus Wahlberg (Diptera: Dolichopodidae) from Singapore and adjacent regions: A long term study with a prudent reconciliation of a genetic to a classic morphological approach
Fig. 1. Present extension of Singapore's mangroves (in green). The numbers indicate the sites that were sampled during the 1-month Singapore Mangrove Insect Project (SMIP 2009); and the 2-year Mangrove Insect Project (MIP 2012-2014). 1, Mandai mangroves; 2, Kranji Nature Trail; 3, Sungei Buloh Wetland Reserve; 4, Lim Chu Kang; 5, Sarimbun mangroves; 6, Berlayer Creek; 7, Pulau Semakau original or old mangrove (SMO); 8, Pulau Semakau, replanted or new mangrove (SMN); 9, Changi creek; 10, Pulau Tekong; 11, Pulau Ubin, Chek Jawa; 12, Pasir Ris; 13, Pulau Seletar; 14, Sungei Cina.
Fig. 4 in Revision of the genus Thinophilus Wahlberg (Diptera: Dolichopodidae) from Singapore and adjacent regions: A long term study with a prudent reconciliation of a genetic to a classic morphological approach
Fig. 4. Thinophilus apicatus sp. nov., male. A, Detail of surstyli ventrally; B, Tips cerci dorsally; C, Ventral view of epandrium; D, Lateral view of epandrium.
Fig. 3 in Revision of the genus Thinophilus Wahlberg (Diptera: Dolichopodidae) from Singapore and adjacent regions: A long term study with a prudent reconciliation of a genetic to a classic morphological approach
Fig. 3. Thinophilus apicatus sp. nov., male. A, Mid femur; B, Hind femur; C, Posterior view of fore leg; D, Anterior view of fore coxa.
Fig. 2 in An Examination Of Call And Genetic Variation In Three Wide-Ranging Southeast Asian Anuran Species
Fig. 2. Spectrograms of Polypedates leucomystax calls from Singapore (top) and Thailand (bottom). Calls are from a single individual in each population. For the Thai individual, call elements did not occur consecutively, but were cut and pasted from a 5 minute recording.
Figure 2 in Scientific Opinion on a notification (reference C/NL/09/02) for the placing on the market of the genetically modified carnation IFD-26407-2 with a modified colour, for import of cut flowers for ornamental use, under Part C of Directive 2001/18/EC from Florigene
Figure 2. - Neobythites bimarginatus. Pelvic-fin length and horizontal eye diameter showing negative allometric growth.
Figure 1 in Scientific Opinion on a notification (reference C/NL/09/02) for the placing on the market of the genetically modified carnation IFD-26407-2 with a modified colour, for import of cut flowers for ornamental use, under Part C of Directive 2001/18/EC from Florigene
Figure 1. - Neobythites bimarginatus Fourmanoir & Rivaton, 1979. SAIAB 189024, SL 122 mm. From off Madagascar (photo M. Krag, ZMUC).
Figure 3 in Genetic, morphometric and meristic analyses of first Acanthurus monroviae specimens recorded in Maltese waters (Central Mediterranean)
Figure 3. – Second specimen of Acanthurus monroviae caught from the Grand Harbour breakwater on 13 October 2015 (Image by A. Vella, CBRGUoM).
Figure 2 in Genetic, morphometric and meristic analyses of first Acanthurus monroviae specimens recorded in Maltese waters (Central Mediterranean)
Figure 2. – First specimen of Acanthurus monroviae caught off St Thomas bay on 28 September 2013 (Image by A. Vella, CBRG-UoM).
Fig. 5. Phylogenetic tree depicting inferred genetic relationships among Leucocytozoon mitochondrial DNA cytochrome b in Negligible evidence for detrimental effects of Leucocytozoon infections among Emperor Geese (Anser canagicus) breeding on the Yukon-Kuskokwim Delta, Alaska
Fig. 5. Phylogenetic tree depicting inferred genetic relationships among Leucocytozoon mitochondrial DNA cytochrome b haplotypes identified from blood samples collected from Emperor Geese inhabiting the Yukon-Kuskokwim Delta, Alaska during 2006–2016 and those previously reported for closely related haemosporidian morphospecies on the National Center for Biotechnology Information GenBank and Malavi databases (accession IDs in parentheses). Bars to the right of tree represent the assignment of sequences to L. simondi clade A (teal), L. simondi clade B (orange), or other Leucocytozoon. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 4. Phylogenetic tree depicting inferred genetic relationships among Haemoproteus mitochondrial DNA cytochrome b in Negligible evidence for detrimental effects of Leucocytozoon infections among Emperor Geese (Anser canagicus) breeding on the Yukon-Kuskokwim Delta, Alaska
Fig. 4. Phylogenetic tree depicting inferred genetic relationships among Haemoproteus mitochondrial DNA cytochrome b haplotypes identified from blood samples collected from Emperor Geese inhabiting the Yukon-Kuskokwim Delta, Alaska during 2006–2016 and those previously reported for closely related haemosporidian morphospecies on the National Center for Biotechnology Information GenBank and Malavi databases (accession IDs in parentheses).
Fig. 5 in Prevalence and genetic diversity of Haemoproteus and Plasmodium in raptors from Thailand: Data from rehabilitation center
Fig. 5. Heatmap of pairwise genetic distances estimated from nucleotide sequences of the cytochrome b gene (479 nucleotides) of Plasmodium spp. using the JukesCanter model.
Fig. 4 in Prevalence and genetic diversity of Haemoproteus and Plasmodium in raptors from Thailand: Data from rehabilitation center
Fig. 4. Bayesian phylogeny based on the partial cytochrome b gene (479 base pairs) of Plasmodium lineages. The lineages isolated in this study are given in red bold. MalAvi lineage codes and GenBank accession numbers are given after species names. Node values indicate percentages of posterior probabilities. Plasmodium isolated from this study are clustered into three clades (clade I, II and II). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 6 in Prevalence and genetic diversity of Haemoproteus and Plasmodium in raptors from Thailand: Data from rehabilitation center
Fig. 6. Haemoproteus spp. infected in Blyth's hawk-eagles (Spizaetus alboniger), KU549 (A-C) and KU589 (D-F). Young gametocytes (A&D), microgametocytes (B&E) and macrogametocytes (C&F). Giemsa staining.
Fig. 2 in Prevalence and genetic diversity of Haemoproteus and Plasmodium in raptors from Thailand: Data from rehabilitation center
Fig. 2. Bayesian phylogeny based on partial cytochrome b gene (479 nucleotides) of Haemoproteus lineages. The lineages isolated in this study are given in red bold. MalAvi lineage codes and GenBank accession numbers are given after species names. Node values indicate percentages of posterior probabilities. Vertical bars indicate clades of subgenus Haemoproteus (A) and Parahaemoproteus (B) Haemoproteus isolated from this study are clustered into two clades (clade I and II). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 3 in Prevalence and genetic diversity of Haemoproteus and Plasmodium in raptors from Thailand: Data from rehabilitation center
Fig. 3. Heatmap of pairwise genetic distances estimated from nucleotide sequences of the cytochrome b gene (479 nucleotides) of Haemoproteus spp. using the JukesCanter model.
Fig. 1 in Prevalence and genetic diversity of Haemoproteus and Plasmodium in raptors from Thailand: Data from rehabilitation center
Fig. 1. Localities of the raptors included in this study. There were 30 provinces where the raptors are found and submitted into the Kasetsart University Raptor Rehabilitation Unit. These provinces are divided into four groups base on the number of raptors. Bangkok is the most common locality of raptor (n> 100).
Fig. 3 in First report of the nematode Cruzia tentaculata using molluscs as natural intermediate hosts, based on morphology and genetic markers
Fig. 3. Scanning Electron Microscope images of a Cruzia tentaculata larvae recovered from Achatina fulica: A) Anterior extremity and detail of the apical view showing the oral opening; B) Cephalic extremity with labial papillae and phasmids (arrows), apical view; C) Lateral view showing the lateral line (arrow); D) posterior region, lateral view showing the lateral line (arrow); E) posterior region, ventral view, and (e) detail of the anus.
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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.