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FIGURE 2 in Relocation of Alona manueli Sinev & Zawisza 2013 and a new closely related species from the Ecuadorian Andes to the new genus Alpinalona (Cladocera, Chydoridae, Aloninae)
FIGURE 2. Alpinalona cajasi sp. nov. from the Cajas National Park, Azuay Province, Ecuador. A–H, adult parthenogenetic female. A, limb I. B, limb II. C, exopodite of limb III. D-E, inner portion of limb III. F, inner portion of limb IV. G, exopodite of limb IV. H, limb V. I, ventral margin, IDL and copulatory hook of limb I of adult male.
FIGURE 1 in Relocation of Alona manueli Sinev & Zawisza 2013 and a new closely related species from the Ecuadorian Andes to the new genus Alpinalona (Cladocera, Chydoridae, Aloninae)
FIGURE 1. Alpinalona cajasi sp. nov. from the Cajas National Park, Azuay Province, Ecuador. A-I, adult parthenogenetic female. A, habitus. B, left valve. C, posteroventral angle of valve. D, marginal setae of anterior part of valve. E, head shield. F, head pores and posterior margin of head shield. G, labrum. H, antennule. I, left antenna.
FIGURE 3 in Relocation of Alona manueli Sinev & Zawisza 2013 and a new closely related species from the Ecuadorian Andes to the new genus Alpinalona (Cladocera, Chydoridae, Aloninae)
FIGURE 3. Alpinalona cajasi sp. nov. from the Cajas National Park, Azuay Province, Ecuador. A–B, adult parthenogenetic female postabdomen. C, ephippial female. D, adult male. E, adult male postabdomen. E, adult male antennule. Limb II triangle-rounded (Fig. 3B). Exopodite elongated, of irregular shape, with short seta.
FIGURE 4 in New species of ptyctimous mites (Acari, Oribatida) from the Peruvian Andes
FIGURE 4. Austrophthiracarus pachiteaensis sp. nov. A—prodorsum, lateral view; B—trichobothrium, lateral view; C— prodorsum, dorsal view; D—trichobothrium, dorsal view; E—opisthosoma, lateral view; F–mentum of subcapitulum; G—right genitoaggenital plate; H—right anoadanal plate; I—trochanter and femur of leg I. Scale bars 100 µm (A, C, E), 50 µm (G, H), 25 µm (B, D, F, I).
FIGURE 6 in New species of ptyctimous mites (Acari, Oribatida) from the Peruvian Andes
FIGURE 6. Notophthiracarus quasipedanos sp. nov. A—prodorsum, lateral view; B—prodorsum, dorsal view; C—opisthosoma, lateral view; D—mentum of subcapitulum; E—right genitoaggenital plate; F—right anoadanal plate G—trochanter and femur of leg I. Scale bars 100 µm (C), 50 µm (A, B, E, F), 25 µm (D, G).
FIGURE 7 in New species of ptyctimous mites (Acari, Oribatida) from the Peruvian Andes
FIGURE 7. Mesotritia curviseta (Hammer, 1961). A—rear lower opisthosoma lateral view with eggs; B—ovipositor (drawn from small individual). Scale bars 100 µm (A), 25 µm (B).
FIGURE 3 in New species of ptyctimous mites (Acari, Oribatida) from the Peruvian Andes
FIGURE 3. Austrophthiracarus conchamarcensis sp. nov. A—prodorsum, lateral view; B—trichobothrium, lateral view; C—prodorsum, dorsal view; D—trichobothrium, dorsal view; E—opisthosoma, lateral view; F—mentum of subcapitulum; G—right genitoaggenital plate; H—anoadanal plates; I—trochanter and femur of leg I. Scale bars 100 µm (A, C, E), 50 µm (G, H), 25 µm (B, D, F, I).
FIGURE 5 in New species of ptyctimous mites (Acari, Oribatida) from the Peruvian Andes
FIGURE 5. Notophthiracarus churubambensis sp. nov. A—prodorsum, lateral view; B—trichobothrium, lateral view; C— prodorsum, dorsal view; D—trichobothrium, dorsal view; E—opisthosoma, lateral view; F—mentum of subcapitulum; G— right genitoaggenital plate; H—right anoadanal plate; I—trochanter and femur of leg I. Scale bars 100 µm (A, C, E), 50 µm (G, H), 25 µm (B, D, F, I).
FIGURE 1 in New species of ptyctimous mites (Acari, Oribatida) from the Peruvian Andes
FIGURE 1. Representatives of newly reported species of box mites from Peruvian Andes– habitus. A—Austrophthiracarus pachiteaensis sp. nov.; B—Notophthiracarus quasipedanos sp. nov. Scale bars 100 µm (A, B).
FIGURE 2 in New species of ptyctimous mites (Acari, Oribatida) from the Peruvian Andes
FIGURE 2. Mesotritia andina sp. nov. A—prodorsum, lateral view; B—prodorsum, dorsal view; C —opisthosoma, lateral view; D—mentum of subcapitulum; E—anogenital region, ventral view; F—trochanter and femur of leg I. Scale bars 100 µm (A, B, C, E), 50 µm (D, F).
Figure 3 in Taxonomic inflation and a reconsideration of speciation in the Andes: the case of the high-elevation tree frog Dendropsophus molitor (Anura: Hylidae)
Figure 3. Comparison of morphometric variation between D. molitor and D. luddeckei. A, PCA plot that represents morphometric differences along the first two PC axes (cumulative explanation of variance ~40%). B, Composition plot for the discriminant analysis, which shows membership probability for each individual. C, Distribution of BIC values for Model-Based Clustering Analysis. The best fit model was 'ellipsoidal, equal volume' (EVV).
Figure 2 in Taxonomic inflation and a reconsideration of speciation in the Andes: the case of the high-elevation tree frog Dendropsophus molitor (Anura: Hylidae)
Figure 2. Bayesian species delimitation test (iBPP) with an integrated dataset. Each node of the tree indicates the posterior probabilities of Bayesian species delimitations inferred under nine different combinations of priors on theta and tau obtained from a Gamma distribution. Each of the resulting posterior probabilities for the different combinations of theta and tau are colour coded and indicated in 3 × 3 boxes on each node. The large 3 × 3 inset indicates the position of each prior combination in these boxes. Species that belong to the 'molitor' group (D. molitor, D. luddeckei, D. meridensis, D. pelidnus) showed very low support (posterior probability) as different species for all theta and tau combinations in contrast to the other Dendropsophus species.
Figure 4 in Taxonomic inflation and a reconsideration of speciation in the Andes: the case of the high-elevation tree frog Dendropsophus molitor (Anura: Hylidae)
Figure 4. MC1R coding region test for association with colour polymorphism. A, Haplotype network for MC1R including D. molitor (green, variegated, and brown) and O. histrionica (black and brown) individuals. Haplotypes of D. molitor did not clustered in association with colour pattern, whereas O. histrionica showed different haplotypes for brown and black dorsal background colour patterns. B, SNPs found in the 557 bp fragment of the coding region of MC1R amplified for D. molitor in comparison with O. histrionica. The alignment shows a 34 bp region (from 409 bp to 443 bp) of this gene. Each morphotype for D. molitor (green, variegated, and brown) and O. histrionica (black and brown) is represented by coloured vertical bars at the right of the alignment. Positions highlighted in a red box indicate Δ433 and C432A mutations responsible for differences in darker dorsal background colour patterns in O. histrionica (Posso-Terranova and Andrés 2017).
Figure 1 in Taxonomic inflation and a reconsideration of speciation in the Andes: the case of the high-elevation tree frog Dendropsophus molitor (Anura: Hylidae)
Figure 1. Distribution, phenotypic variation, and phylogenetic relationships for D. molitor and D. luddeckei. A, Map of the sampling localities. Triangles: sampling points for the putative species D. luddeckei. Circles: sampling points for D. molitor. Additional information for each sample and locality is given in Supporting Information, Table S1. The vertical dashed line delineates the contact zone between both putative species proposed by Guarnizo et al. (2012) B, Colour polymorphism of D. molitor is defined as three morphotypes: solid green, variegated and solid brown in order from top to bottom. Photographs by the authors. C, Bayesian consensus phylogenetic tree based on mtDNA markers (12S, 16S, and COI). Nodes show the bootstrap support on the left and the posterior probability on the right. Nodes indicating only the posterior probability were not supported by ML bootstrap and nodes without values were not supported by both ML and BI. Asterisks next to sample names in the phylogeny indicate the individuals added in this study. Colour and symbol codes are as described in panel A. Vertical bars at the right of the phylogeny show the results of the ASAP and bPTP species delimitation tests.
FIGURE 5 in A new species of tanager (Aves: Thraupidae) from the Eastern slopes of the Andes
FIGURE 5. Distribution of Trichothraupis melanops (orange) and T. griseonota sp. nov. (green) in South America. Squares represent museum specimens and circles are recordings. A diamond indicates the type locality of T. griseonota; there is no type locality for T. melanops. South America is represented in the inset.
FIGURE 4 in A new species of tanager (Aves: Thraupidae) from the Eastern slopes of the Andes
FIGURE 4. Trichothraupis melanops (above) and T. griseonota sp. nov. (below). Plate by Eduardo Brettas.
FIGURE 3 in A new species of tanager (Aves: Thraupidae) from the Eastern slopes of the Andes
FIGURE 3. Principal Component Analysis of Atlantic Forest (orange) and Andean (green) populations of Trichothraupis melanops. No morphometric segregation was found for males (A) or females (B).
FIGURE 1 in A new species of tanager (Aves: Thraupidae) from the Eastern slopes of the Andes
FIGURE 1. Dorsal (a), ventral (b), and lateral (c) views of males of the Atlantic (LSUMZ 53115, Itapetininga, Brazil; above) and Andean (LSUMZ 171459, Samipata, Bolivia; below) populations of Trichothraupis melanops.
FIGURE 3 in A new species of Centrozoros Kukalová-Peck & Peck, 1993 (Zoraptera: Spiralizoridae) from high elevations in the northwestern Andes of Colombia
FIGURE 3. Centrozoros mesenia sp. nov., holotype, male. A) Habitus, dorsal. B) Habitus, lateral. C) Head, dorsal. D) Thorax, dorsal. E) Metafemur, posterior. F) Abdomen, dorsal. Scales: A, B, D‒F: 0.5 mm; C: 0.2 mm.
FIGURE 1 in A new species of Centrozoros Kukalová-Peck & Peck, 1993 (Zoraptera: Spiralizoridae) from high elevations in the northwestern Andes of Colombia
FIGURE 1. Distribution map of Centrozoros species known from Colombia. Bibliographical references of previous geographic records from Colombia are indicated by black circles; the white star indicates the location of Centrozoros mesenia sp. nov.
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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.