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509 results for “Zoogeography”
Figure 26 in Systematic revision of Neotropical Achalcus and a related new genus (Diptera: Dolichopodidae, Achalcinae) with comments on their phylogeny, ecology and zoogeography
Figure 26. Australachalcus variabilis sp. nov. (male). A, femur II; B, wing; C, antenna; D, hypopygium.
Figure 25 in Systematic revision of Neotropical Achalcus and a related new genus (Diptera: Dolichopodidae, Achalcinae) with comments on their phylogeny, ecology and zoogeography
Figure 25. Australachalcus setosus sp. nov. (male). A, femur I; B, femur II; C, antenna; D, wing; E, hypopygium.
Figure 24 in Systematic revision of Neotropical Achalcus and a related new genus (Diptera: Dolichopodidae, Achalcinae) with comments on their phylogeny, ecology and zoogeography
Figure 24. Australachalcus robustus sp. nov. (male). A, wing; B, hypopygium; C, antenna; D, coxa and femur I; E, femur II.
Figure 16 in Systematic revision of Neotropical Achalcus and a related new genus (Diptera: Dolichopodidae, Achalcinae) with comments on their phylogeny, ecology and zoogeography
Figure 16. Australachalcus browni sp. nov. (male). A, wing; B, femur II; C, antenna; D, femur I; E, hypopygium.
Figure 21 in Systematic revision of Neotropical Achalcus and a related new genus (Diptera: Dolichopodidae, Achalcinae) with comments on their phylogeny, ecology and zoogeography
Figure 21. Australachalcus longicornis (Van Duzee) (male). A, wing; B, antenna; C, coxa and femur I; D, femur III, posterior view.
Figure 12 in Systematic revision of Neotropical Achalcus and a related new genus (Diptera: Dolichopodidae, Achalcinae) with comments on their phylogeny, ecology and zoogeography
Figure 12. Australachalcus acornis sp. nov. (male). A, femur I; B, femur II; C, antenna; D, wing; E, hypopygium.
Figure 13 in Systematic revision of Neotropical Achalcus and a related new genus (Diptera: Dolichopodidae, Achalcinae) with comments on their phylogeny, ecology and zoogeography
Figure 13. Australachalcus albipalpus (Parent) (male, unless mentioned otherwise). A, wing; B, female antenna; C, antenna; D, hypopygium; E, epandrial setae at base of epandrial lobe.
Figure 5 in Systematic revision of Neotropical Achalcus and a related new genus (Diptera: Dolichopodidae, Achalcinae) with comments on their phylogeny, ecology and zoogeography
Figure 5. Achalcus costaricensis sp. nov. (male, unless mentioned otherwise). A, wing; B, coxa and femur I; C, antenna; D, female antenna; E, palp; F, hypopygium.
Figure 1 in Systematic revision of Neotropical Achalcus and a related new genus (Diptera: Dolichopodidae, Achalcinae) with comments on their phylogeny, ecology and zoogeography
Figure 1. Achalcus flavicollis (Meigen) (male). Hypopygium. AE, aedeagus; CC, cercus; DEP, dorsal process of epandrium; EL, epandrial lobe; ES, epandrial setae; HP, hypandrium; PGO, postgonites; ST, surstylus; VEP, ventral process of epandrium.
Figure 5. A, strict consensus tree from 11 in A new leptarctine (Carnivora: Mustelidae) from the early Miocene of the northern Tibetan Plateau: implications for the phylogeny and zoogeography of basal mustelids
Figure 5. A, strict consensus tree from 11 shortest trees (tree length = 79 steps) recovered using the Branch and Bound option in PAUP (Swofford, 1993) on a 17 ¥ 31 data matrix (Table 2); B, bootstrap analysis performed on the same data matrix. Numbers at the nodes indicate per cent bootstrap support from heuristic search based on 100 replicates. Only groups with a frequency of greater than 50% are retained.
Figure 1 in A new leptarctine (Carnivora: Mustelidae) from the early Miocene of the northern Tibetan Plateau: implications for the phylogeny and zoogeography of basal mustelids
Figure 1. Above, map of the Tabenbuluk (Danghe) area in the Tibetan Plateau. Below, map of selected vertebrate fossil localities and their geological relationships in the Danghe area (adapted from Wang et al., 2003c: fig. 2). Only the early Miocene localities in the Xishuigou Fauna are plotted (in upper right quadrant), along with the late Oligocene Yindirte Fauna (in lower left quadrant).
Figure 6 in A new leptarctine (Carnivora: Mustelidae) from the early Miocene of the northern Tibetan Plateau: implications for the phylogeny and zoogeography of basal mustelids
Figure 6. Cladogram of basal musteloids. A single tree with a length of 77 was found using the Branch and Bound option in PAUP (Swofford, 1993) on a 16 ¥ 31 data matrix (Table 2). Character distributions were optimized using ClaDos (version 1.2, Kevin Nixon). As ClaDos does not accept a matrix with two-state codings, we converted the two-state characters into a single derived state.
Figure 3 in A new leptarctine (Carnivora: Mustelidae) from the early Miocene of the northern Tibetan Plateau: implications for the phylogeny and zoogeography of basal mustelids
Figure 3. Holotype of Kinometaxia guangpui gen. et sp. nov., IVPP V13057, A, stereophotos of occlusal view of upper left P4 and M1; B, anterior and C, posterior views of skull.
Figure 2 in A new leptarctine (Carnivora: Mustelidae) from the early Miocene of the northern Tibetan Plateau: implications for the phylogeny and zoogeography of basal mustelids
Figure 2. Holotype of Kinometaxia guangpui gen. et sp. nov., IVPP V13057, A, lateral, B, ventral, and C, dorsal views.
Figure 7 in A new leptarctine (Carnivora: Mustelidae) from the early Miocene of the northern Tibetan Plateau: implications for the phylogeny and zoogeography of basal mustelids
Figure 7. Phyletic relationships, time ranges, and migration events of Eurasian and North American late Cenozoic leptarctines and some basal mustelids. The first appearance datums (FAD) are derived from the following sources: Paragale and Plesiogale from the late Aquitanian Montaigu-le-Blin locality in the Allier Basin of France (MN2a, c. 20.5–22.5 Mya) (Ginsburg, 1999), Trocharion from Vieux Collonges (MN 5, 17–15 Mya) of France (Qiu & Schmidt- Kittler, 1982), Kinometaxia from the IVPP DH 9910 locality in the Tiejianggou Formation (Wang et al., 2003c), North America leptarctines (Schultzogale, Craterogale, and Leptarctus) from the early Hemingfordian Runningwater Formation of Nebraska (Baskin, 1998; Lim & Martin, 2000), and Leptarctus neimenguensis from the late Tunggurian Tairum Nor locality in the Tunggur Formation of China (Zhai, 1964; Wang et al., 2003b). Open arrows pointing right and left indicate eastward and westward migration events respectively.
Figs 60-66 in On the taxonomy and zoogeography of some Palaearctic Paederinae and Xantholinini (Coleoptera: Staphylinidae)
Figs 60-66: Xantholinus graecus KRAATZ (60-62), X. varnensis COIFFAIT (63-64), and X. minos nov.sp. (65-66): aedeagus in dorsal or in ventral view of lectotype (60), paratypes (65-66), and males from Mersin (61), Pelopónnisos (62), Muğla (63), and Karpathos (64). Scale bar: 0.5 mm.
Figs 48-54 in On the taxonomy and zoogeography of some Palaearctic Paederinae and Xantholinini (Coleoptera: Staphylinidae)
Figs 48-54: Lobrathium reuteri nov.sp. (48-52) and L. schillhammeri ASSING & SCHÜLKE (53-54): (48) female tergite VIII; (49) female sternite VIII; (50) female segments IX-X; (51-54) ventral process of aedeagus in ventral and in lateral view. Scale bars: 48-50: 0.5 mm; 51-54: 0.2 mm.
Figs 37-39 in On the taxonomy and zoogeography of some Palaearctic Paederinae and Xantholinini (Coleoptera: Staphylinidae)
Figs 37-39: Tetartopeus sengleti BORDONI, holotype (37-38) and T. persicus COIFFAIT from Iraq (39): (37) forebody; (38-39) aedeagus in lateral view. Scale bars: 37: 1.0 mm; 38-39: 0.2 mm.
Map 1 in On the taxonomy and zoogeography of some Palaearctic Paederinae and Xantholinini (Coleoptera: Staphylinidae)
Map 1: Distribution of Pseudomedon dido (Saulcy). Filled circles: examined records; open circle: type locality.
Figs 6-13 in On the taxonomy and zoogeography of some Palaearctic Paederinae and Xantholinini (Coleoptera: Staphylinidae)
Figs 6-13: Lithocharis schuelkei nov.sp.: (6) habitus; (7) forebody; (8) antenna; (9) male sternite VII; (10) male sternite VIII; (11-12) aedeagus in lateral and in ventral view; (13) ventral process of aedeagus in ventral view. Scale bars: 6-8: 1.0 mm; 9-12: 0.5 mm; 13: 0.1 mm.
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.