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Figures 1–3 in Sundapyrochroa: A new genus of Fire-Colored Beetles (Coleoptera: Pyrochroidae: Pyrochroinae) from the Sunda Shelf, with a key to the three species

Figures 1–3. Sundapyrochroa atricolor (Pic). 1) Habitus, adult male, dorsal. 2) Left antenna, lateroventral. 3) Habitus, adult female, dorsal.

opencc-by-4.0Jan 2014View details →
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Figures 22–23 in Sundapyrochroa: A new genus of Fire-Colored Beetles (Coleoptera: Pyrochroidae: Pyrochroinae) from the Sunda Shelf, with a key to the three species

Figures 22–23. Two species of Pyrochroidae. 22) Dendroides canadensis Latreille, habitus adult male, dorsal. 23) Sinodendroides chinensis Young, habitus adult male, dorsal.

opencc-by-4.0Jan 2014View details →
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Figures 7–8 in Sundapyrochroa: A new genus of Fire-Colored Beetles (Coleoptera: Pyrochroidae: Pyrochroinae) from the Sunda Shelf, with a key to the three species

Figures 7–8. Sundapyrochroa nigripennis (Pic). 7) Head, adult male, dorsal. 8) Left antenna, dorsolateral.

opencc-by-4.0Jan 2014View details →
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Supplementary material to "Exogenous corticosterone and melanin-based coloration explain variation in juvenile dispersal behaviour in the barn owl (Tyto alba)"

<p><strong>Abstract</strong></p> <p>Natal dispersal affects many processes such as population dynamics. So far, most studies have examined the intrinsic and extrinsic factors that determine the distance between the place of birth and of first breeding. In contrast, few researchers followed the first steps of dispersal soon after fledging. To study this gap, we radio-tracked 95 barn owl nestlings (<em>Tyto alba</em>) to locate their diurnal roost sites from the fledging stage until December. This was used to test whether the age of nest departure, post-fledging movements and dispersal distance were related to melanin-based coloration, which is correlated to fitness-related traits, as well as to corticosterone, a hormone that mediates a number of life history trade-offs and the physiological and behavioural responses to stressful situations. We found that the artificial administration of corticosterone delayed the age when juveniles left their parental home-range in females but not in males. During the first few months after fledging, longer dispersal distances were reached by females compared to males, by individuals marked with larger black feather spots compared to individuals with smaller spots, by larger individuals and by those experimentally treated with corticosterone. We conclude that the onset and magnitude of dispersal is sensitive to the stress hormone corticosterone, melanin-based coloration and body size.&nbsp;</p>

opencc-by-nc-4.0Jun 2021View details →
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Fig 1 in A detailed illustrated description of Palearctic species Magwengiella (=Listrocalus) nycthemerops (HEINRICH, 1978). Notes on transformation of pigmental coloration of type specimens (Hymenoptera, Ichneumonidae, Ichneumoninae, Ctenocalini)

Fig 1: Magwengiella (=Listrocalus) nycthemerops (HEINRICH, 1978) paratype from ZSM (photo of St. Schmidt 06.09.2013).

opencc-by-4.0Dec 2015View details →
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Figures 125–126. Color habitus photographs. 125 in New and little known Coleoptera (Silvanidae: Silvaninae) from Central and South America

Figures 125–126. Color habitus photographs. 125) Eunausibius jatahyensis, new species. 126) Annomus bolivianus, new genus, new species.

opencc-by-4.0Dec 2020View details →
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Figures 123–124. Color habitus photographs. 123 in New and little known Coleoptera (Silvanidae: Silvaninae) from Central and South America

Figures 123–124. Color habitus photographs. 123) Synobius lobatus (Grouvelle). 124) Pensus hirtus, new species.

opencc-by-4.0Dec 2020View details →
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Figure 3 in Molecular test shows the color pattern is not so reliable in diagnostic of genus Dysphaea Selys (Odonata: Euphaeidae)

Figure 3. Phylogenetic reconstruction of 37 samples based on combined gene dataset (COI+16S+28S, 2394 bp). Bayesian posterior probabilities (left) and ML bootstrap value (right) are indicated at nodes. Among the central Vietnamese specimens of Dysphaea sp. the ID numbers in red color indicate those specimens with dark colour which were originally identified by us as D. basitincta. Those with ID in green indicate specimens originally identified by us as D. gloriosa. The blue ID refers to D. haomiao.

opencc-by-4.0Dec 2019View details →
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Figure 2 in Molecular test shows the color pattern is not so reliable in diagnostic of genus Dysphaea Selys (Odonata: Euphaeidae)

Figure 2. Photos of the right pair of wings of some male specimens showing the variations of wing color patterns. The wings of the syntype of D. basitincta (at MNHN, Paris) was kindly provided by Matti Hämäläinen.

opencc-by-4.0Dec 2019View details →
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Fig. 14 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico

Fig. 14. Additive tree (phenogram), based on Mahalanobis D2 distances (table 13), depicting meristic resemblance among nine groups of Aspidoscelis tesselata. Distances (similarities) between groups are computed by adding lengths of nodes between groups of interest. Terminal nodes represent the nine groups, and internal nodes represent horizontal distances between clusters. As an interpretation example, the resemblance between Conchas 6C­E and Conchas 1C­E is 7.2 + 3.2 + 2.2 + 2.8 + 5.6 = 21.0, while the resemblance between Conchas 6C­E and Macho E­C is 7.2 + 1.0 + 1.9 + 3.1 = 13.2.

opencc-by-4.0Dec 2003View details →
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Fig. 3 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico

Fig. 3. Electrophoretic phenotypes of sACOH, a monomeric enzyme, from liver homogenates of nine specimens of A. tesselata of pattern class C­E from Conchas Lake State Park, New Mexico. Letters below gel identify allozymes based on alleles present (table 3), and the genotype of each lizard is listed on the right. Lanes for individual lizards are labeled beside their patterns on the gel. Anode is to the right.

opencc-by-4.0Dec 2003View details →
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Fig. 11 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico

Fig. 11. Pattern of multivariate morphological variation among Aspidoscelis tesselata of pattern classes C (N = 44), E (N = 32), and New Mexico D (N = 5) from the vicinity of Sumner Lake State Park, De Baca County, New Mexico. Canonical variate scores were derived from a canonical variate analysis using meristic characters identified in table 10.

opencc-by-4.0Dec 2003View details →
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Fig. 2 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico

Fig. 2. Electrophoretic phenotypes of GPI, a dimeric enzyme, from erythrocyte hemolysates of six specimens of Aspidoscelis. Letters below gel identify allozymes based on alleles present (table 3), and the genotype of each lizard is listed on the right. Note the very slight difference in migration between the products of the b­allele versus c­allele. Lanes for individual lizards are labeled beside their patterns on the gel as follows: TESC, A. tesselata of pattern class C­E from Conchas Lake State Park, New Mexico; and TESE, A. tesselata of pattern class E from Sandoval County, New Mexico. Anode is to the right.

opencc-by-4.0Dec 2003View details →
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Fig. 1 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico

Fig. 1. Geographic relationships among four northern collecting localities of Aspidoscelis tesselata of color pattern classes C, New Mexico D, and E and convenience classes C­E and E­C. Color patterns found at the four sites are (1) Conchas Lake State Park: C­E and New Mexico D; (2) Sumner Lake State Park: C, New Mexico D, and E; (3) Puerto de Luna: E; and (4) Arroyo del Macho: E­C.

opencc-by-4.0Dec 2003View details →
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Fig. 7 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico

Fig. 7. Color pattern variation in Aspidoscelis tesselata of pattern class C­E from the vicinity of Conchas Lake State Park, San Miguel County, New Mexico. Morphological subgroup 6C­E: A (RU 0002, 93 mm SVL); B (RU 0029, 96 mm SVL); morphological subgroup 1C­E: C (RU 0013, 95 mm SVL); D (RU 0030, 89 mm SVL); E (RU 0021, 95 mm SVL); morphological subgroup 8C­E: F (RU 0027, 86 mm SVL).

opencc-by-4.0Dec 2003View details →
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Fig. 4 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico

Fig. 4. Electrophoretic phenotypes of MPI, a monomeric enzyme, from liver homogenates of 11 specimens of Aspidoscelis. Letters below gel identify allozymes based on alleles present (table 3), and the genotype of each lizard is listed on the right. Lanes for individual lizards are labeled beside their patterns on the gel (with genotype) as follows: NEOTESA, B, and C, different pattern classes of the triploid A. neotesselata from Colorado; TESC and D, A. tesselata of pattern classes C­E and D from Conchas Lake State Park, New Mexico; TESE, A. tesselata of pattern class E­C from Arroyo del Macho, New Mexico; TESF, A. dixoni from New Mexico; TESF × PUN, triploid hybrid of A. dixoni × A. tigris punctilinealis from New Mexico; and TESG and H, A. dixoni of two pattern classes from Texas. Anode is to the right.

opencc-by-4.0Dec 2003View details →
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Fig. 3 in Evidence of the color pattern variation in populations of Gymnotus pantanal (Gymnotiformes) from three streams in the upper Paraná River basin, Brazil

Fig. 3. Color pattern variation in Gymnotus pantanal from Pinheirinho and Jacutinga streams. (a) 209.8 mm TL (NUP 9311); (b) 181.0 mm TL (NUP 9311); (c) 150.0 mm TL (NUP 9312); (d) 125.0 mm TL (NUP 9312).

opencc-by-4.0May 2011View details →
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Fig. 4 in Evidence of the color pattern variation in populations of Gymnotus pantanal (Gymnotiformes) from three streams in the upper Paraná River basin, Brazil

Fig. 4. Principal Component Analysis (PCA) ordination (a) and average values (± standard error) of the axes scores 1 (b) and 2 (c) from PCA ordination of morphometric characters for Gymnotus pantanal atypical color pattern (G. 1) and Gymnotus pantanal sensu stricto (G. 2).

opencc-by-4.0May 2011View details →
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Fig. 2 in Scientific Note Ambicoloration and morphological aberration in the sole Achirus declivis (Pleuronectiformes: Achiridae) and two other cases of color abnormalities in achirid soles from southeastern Brazil

Fig. 2. Incomplete eye rotation and incomplete development of the dorsal fin over the skull in the plainfin sole Achirus declivis (UFES 0095; 94.9 mm SL) from the Piraquê-Açú River, Espírito Santo, southeast Brazil: (a) ocular side; (b) detail of blind side of the head; (c) ocular side of the head; (d) radiograph of the head. Photographs by Raphael M. Macieira.

opencc-by-4.0Jun 2006View details →
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Fig. 1 in Scientific Note Ambicoloration and morphological aberration in the sole Achirus declivis (Pleuronectiformes: Achiridae) and two other cases of color abnormalities in achirid soles from southeastern Brazil

Fig. 1. Abnormal pigmentation patterns in the plainfin sole Achirus declivis from the Piraquê-Açú River, Espírito Santo, southeast Brazil: (a) ocular side of ambicolored 108.8 mm SL specimen (ZUEC 6274); (b) blind side of the individual represented in a; (c) ocular side of hypomelanistic specimen 119.1 mm SL (ZUEC 6275); (d) blind side of the individual represented in c. Photographs by Raphael M. Macieira.

opencc-by-4.0Jun 2006View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record