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Figure 2B from: Leray VL, Caravas J, Friedrich M, Zigler KS (2019) Mitochondrial sequence data indicate "Vicariance by Erosion" as a mechanism of species diversification in North American Ptomaphagus (Coleoptera, Leiodidae, Cholevinae) cave beetles. Subterranean Biology 29: 35-57. https://doi.org/10.3897/subtbiol.29.31377

Figure 2B Distribution of hirtus-group species. All known sites for members of the South Cumberlands lineage in Tennessee and Alabama. Exposed karst is shown in gray.

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Figure 2A from: Leray VL, Caravas J, Friedrich M, Zigler KS (2019) Mitochondrial sequence data indicate "Vicariance by Erosion" as a mechanism of species diversification in North American Ptomaphagus (Coleoptera, Leiodidae, Cholevinae) cave beetles. Subterranean Biology 29: 35-57. https://doi.org/10.3897/subtbiol.29.31377

Figure 2A Distribution of hirtus-group species. All known sites for hirtus-group species in Kentucky, Tennessee, Alabama, and Georgia. P.shapardi sites in Oklahoma and Arkansas are indicated in upper right inset map. A dozen species from the southern Cumberland Plateau in Tennessee and Alabama are combined.

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Figure 6 from: Ichiishi W, Shimada S, Motobayashi T, Abe H (2019) Completely engaged three-dimensional mandibular gear-like structures in the adult horned beetles: reconsideration of bark-carving behaviors (Coleoptera, Scarabaeidae, Dynastinae). ZooKeys 813: 89-110. https://doi.org/10.3897/zookeys.813.29236

Figure 6 Gear-like structures on mandibles of adult horned beetles. To show the mandibular gear-like structure, the head was split along the anterior midline, and the mandibles were laid out and viewed from the inside. A Mandibles of a T.dichotomus male adult B diagram of structures in Fig. 6A; gear-like structures are shown as stipple. Arrows indicate the tip of each tooth. Scale bar: 2 mm.

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Figure 4 from: Rohner PT, Haenni J-P, Giesen A, Busso JP, Schäfer MA, Püchel-Wieling F-W, Blanckenhorn WU (2019) Temporal niche partitioning of Swiss black scavenger flies in relation to season and substrate age (Diptera, Sepsidae). Alpine Entomology 3: 1-10. https://doi.org/10.3897/alpento.3.28366

Figure 4 Number of individuals of seven common sepsid species as a function of dung age (in hours (h)). While S.cynipsea, flavimana and orthocnemis are disproportionally often observed on fresh dung, S.duplicata and Saltellasphondylii gain in relative abundance over time. (Note the different scaling of the y-axes; data from Püchel 1993; S.duplicata data only qualitative.)

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Figure 2 from: Ichiishi W, Shimada S, Motobayashi T, Abe H (2019) Completely engaged three-dimensional mandibular gear-like structures in the adult horned beetles: reconsideration of bark-carving behaviors (Coleoptera, Scarabaeidae, Dynastinae). ZooKeys 813: 89-110. https://doi.org/10.3897/zookeys.813.29236

Figure 2 Measurements of mandible strengths of break resistance. AT.dichotomus horns were fixed in a small vice B wire was hung on the tip of the mandible.

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Figure 3 from: Rohner PT, Haenni J-P, Giesen A, Busso JP, Schäfer MA, Püchel-Wieling F-W, Blanckenhorn WU (2019) Temporal niche partitioning of Swiss black scavenger flies in relation to season and substrate age (Diptera, Sepsidae). Alpine Entomology 3: 1-10. https://doi.org/10.3897/alpento.3.28366

Figure 3 Non-metric multidimensional scaling (NMDS) visualizing seasonal variation in species composition as well as differences between cattle pastures (triangles) and dung piles (circles). The smaller the distance between two samples, the greater their similarity.

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Figure 2 from: Rohner PT, Haenni J-P, Giesen A, Busso JP, Schäfer MA, Püchel-Wieling F-W, Blanckenhorn WU (2019) Temporal niche partitioning of Swiss black scavenger flies in relation to season and substrate age (Diptera, Sepsidae). Alpine Entomology 3: 1-10. https://doi.org/10.3897/alpento.3.28366

Figure 2 Seasonal patterns of species diversity, expressed by the first three Hill indices, for sepsid communities captured by sweep netting on cow pastures, dung piles or Malaise capturing in a peat bog. 0D equals species richness, 1D represents the exponential Shannon entropy (evenness) that can be interpreted as the number of typical species, while 2D resembles the reciprocal form of the Gini-Simpson Index that relates to the number of highly abundant species. We only plotted samples with 20 or more individuals (all years combined). The size of the points is proportional to the number of individuals present in the sample.

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Figure 4 from: Leray VL, Caravas J, Friedrich M, Zigler KS (2019) Mitochondrial sequence data indicate "Vicariance by Erosion" as a mechanism of species diversification in North American Ptomaphagus (Coleoptera, Leiodidae, Cholevinae) cave beetles. Subterranean Biology 29: 35-57. https://doi.org/10.3897/subtbiol.29.31377

Figure 4 Distribution of Ptomaphagus species on the southern Cumberland Plateau, overlaid on a digital elevation model. Higher elevations (to 500 m) are indicated by darker shades, lower elevations (to 180 m) by lighter shades. Ptomaphagus species diverging early in the South Cumberlands lineage are limited to isolated ridges and mountains on the fringes of the plateau. These species are P.loedingi (yellow), P.longicornis (dark gray), P.julius (blue), P.solanum (dark green) and P.hazelae (light blue). The colors used here correspond to those in Figure 2B.

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Figure 1 from: Rohner PT, Haenni J-P, Giesen A, Busso JP, Schäfer MA, Püchel-Wieling F-W, Blanckenhorn WU (2019) Temporal niche partitioning of Swiss black scavenger flies in relation to season and substrate age (Diptera, Sepsidae). Alpine Entomology 3: 1-10. https://doi.org/10.3897/alpento.3.28366

Figure 1 Relative abundance of males of different sepsid species across the season on pastures (all years pooled). Patterns are indicated separately for high (blue) and low (green) altitude sites. Species trapped in a Malaise trap are shown in black. Point size is proportional to the total number of males contained in the respective sample.

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Figures 3-7 from: Iturralde GG, Leal-Zanchet AM (2019) Why be original? Two new species of Choeradoplana resembling the type species of the genus in their external aspects (Platyhelminthes, Continenticola). ZooKeys 813: 1-19. https://doi.org/10.3897/zookeys.813.29565

Figures 3-7 Choeradoplanalongivesicula sp. n., paratype MZU PL. 00292 3, 4 pre-pharyngeal region, transverse sections 5, 6 anterior region of body, transverse sections 7 pharynx, sagittal section, with anterior tip to the left.

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Figures 1- 2 from: Iturralde GG, Leal-Zanchet AM (2019) Why be original? Two new species of Choeradoplana resembling the type species of the genus in their external aspects (Platyhelminthes, Continenticola). ZooKeys 813: 1-19. https://doi.org/10.3897/zookeys.813.29565

Figures 1- 2 Choeradoplanalongivesicula sp. n., paratype MZU PL. 00292, 1, 2 dorsal view, with part of whitish ventral surface visible in 1. Arrows indicate the anterior tip.

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Figure 11 from: Bao-Shi Z, Feng Z (2019) Three new species of the genus Zodarion (Araneae, Zodariidae) from China. ZooKeys 813: 67-87. https://doi.org/10.3897/zookeys.813.29683

Figure 11 Zodarionfurcum Zhu, 1988, male holotype (A, B) and female paratype (C, D) Habitus (A, C dorsal view B, D ventral view).

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Figure 5 from: Ichiishi W, Shimada S, Motobayashi T, Abe H (2019) Completely engaged three-dimensional mandibular gear-like structures in the adult horned beetles: reconsideration of bark-carving behaviors (Coleoptera, Scarabaeidae, Dynastinae). ZooKeys 813: 89-110. https://doi.org/10.3897/zookeys.813.29236

Figure 5 Engagement of gear-like structures on mandibles of D.hercules during opening and closing; engaged regions of mandibles were exposed using a file. A Lateral view of the head from the left side; dotted lines indicate the position of the transverse section B interior view of the head from the ventral side C diagram of the engagement region; gear-like structures are emphasized by stipple. Abbreviations: R = right compound eye; L = left compound eye. Scale bar: 7 mm.

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Figures 17- 18 from: Iturralde GG, Leal-Zanchet AM (2019) Why be original? Two new species of Choeradoplana resembling the type species of the genus in their external aspects (Platyhelminthes, Continenticola). ZooKeys 813: 1-19. https://doi.org/10.3897/zookeys.813.29565

Figures 17- 18 Choeradoplanacyanoatria sp. n., holotype, sagittal sections 17 prostatic vesicle 18 ejaculatory duct, and female canal. Anterior tip to the left.

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Figure 1 from: Troncoso-Palacios J, Ruiz De Gamboa M, Langstroth R, Ortiz JC, Labra A (2019) Without a body of evidence and peer review, taxonomic changes in Liolaemidae and Tropiduridae (Squamata) must be rejected. ZooKeys 813: 39-54. https://doi.org/10.3897/zookeys.813.29164

Figure 1 Outline of the non-standard presentation of the three species proposed by Demangel Miranda (2016a).

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Figure 8 from: Ichiishi W, Shimada S, Motobayashi T, Abe H (2019) Completely engaged three-dimensional mandibular gear-like structures in the adult horned beetles: reconsideration of bark-carving behaviors (Coleoptera, Scarabaeidae, Dynastinae). ZooKeys 813: 89-110. https://doi.org/10.3897/zookeys.813.29236

Figure 8 Mandibles and labium of D.hercules; engaged regions of mandibles were exposed using a file. A Interior view of the male head from the dorsal side; arrows indicate projections from the labium into the mouth cavity B lateral view of labium from the left side; arrows indicate projections into the mouth cavity.

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Figure 2 from: Bao-Shi Z, Feng Z (2019) Three new species of the genus Zodarion (Araneae, Zodariidae) from China. ZooKeys 813: 67-87. https://doi.org/10.3897/zookeys.813.29683

Figure 2 Zodarionapertum sp. n., male holotype left palp (A–C) and female paratype (D, E) A Prolateral view B Ventral view C Retrolateral view D Epigynum, ventral view E Vulva, dorsal view.

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Figures 10- 11 from: Iturralde GG, Leal-Zanchet AM (2019) Why be original? Two new species of Choeradoplana resembling the type species of the genus in their external aspects (Platyhelminthes, Continenticola). ZooKeys 813: 1-19. https://doi.org/10.3897/zookeys.813.29565

Figures 10- 11 Choeradoplanalongivesicula sp. n., holotype, sagittal sections 10 prostatic vesicle 11 ejaculatory duct and female canal. Anterior tip to the left. Arrow indicates the transition from the prostatic vesicle to the ejaculatory duct.

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Figure 1 from: Bao-Shi Z, Feng Z (2019) Three new species of the genus Zodarion (Araneae, Zodariidae) from China. ZooKeys 813: 67-87. https://doi.org/10.3897/zookeys.813.29683

Figure 1 Zodarionapertum sp. n., habitus (A, C dorsal view B, D ventral view) A, B Male holotype C, D Female paratype.

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Figure 13 from: Bao-Shi Z, Feng Z (2019) Three new species of the genus Zodarion (Araneae, Zodariidae) from China. ZooKeys 813: 67-87. https://doi.org/10.3897/zookeys.813.29683

Figure 13 Records of Zodarion species in China. ① Zodarionapertum sp. n. ② Zodarionplanum sp. n. ③ Zodarionovatum sp. n. ④ Zodarionchaoyangense Zhu & Zhu, 1983 ⑤ Zodarionfurcum Zhu, 1988 ⑥ Zodarionhunanense Yin, 2012.

opencc-by-4.0Jan 2019View details →

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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.
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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.

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

OpenNeuro

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

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