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Fig. 6 in New species of Eugerres from the Usumacinta Province, México and Guatemala with a redescription of E. mexicanus (Steindachner, 1863) (Teleostei: Gerreidae)
Fig. 6. Premaxillary bone, dorsal view, in (a) Eugerres castroaguirrei ECOSC 5511-1, and (b) E. mexicanus UABC 2666. ap = ascending process, arp = articular process, cp = caudal process, sp = symphysial process. Pharyngeal plates in (c) E. castroaguirrei and (d) E. mexicanus: dorsal view (d.v.) and lateral view (l.v.). pt = pharyngeal dentition.
Fig. 7 in New species of Eugerres from the Usumacinta Province, México and Guatemala with a redescription of E. mexicanus (Steindachner, 1863) (Teleostei: Gerreidae)
Fig. 7. Dorsal fin supports of (a) E. castroaguirrei ECOSC 5511-1, and (b) E. mexicanus UABC 2666. fds = first dorsal spine, sds = second dorsal spine, pr = proximal radial; anal fin supports of (c) E. castroaguirrei and (d) E. mexicanus. fas = first anal spine, sas = second anal spine, pr = proximal radial. Both structures from left side.
Fig. 3. a in New species of Eugerres from the Usumacinta Province, México and Guatemala with a redescription of E. mexicanus (Steindachner, 1863) (Teleostei: Gerreidae)
Fig. 3. a) Eugerres castroaguirrei new species, ECOSC 775, holotype, 184.3 mm SL. México, Chiapas, río Lacantún, Selva Lacandona, Marqués de Comillas, Reforma Agraria and Galaxia; b) Eugerres mexicanus, NMW 72289, lectotype, 165.6 mm SL. México, Tabasco, Flus (río) Teapa.
Fig. 5 in New species of Eugerres from the Usumacinta Province, México and Guatemala with a redescription of E. mexicanus (Steindachner, 1863) (Teleostei: Gerreidae)
Fig. 5. Lateral view of neurocranium of (a) E. castroaguirrei, ECOSC 5511-1, and (b) E. mexicanus UABC 2666. epo = epioccipital, fp = foramen postemporal, pat = parietal, ps = pterosphenoid, sop = supraoccipital process. Lateral view of infraorbital 1 in (c) E. castroaguirrei and (d) E. mexicanus. dap = dorsal apophysis, am = anterior margin, cp = caudal process, for = foramen, vm = ventral margin. Both structures from left side.
Fig. 2. a in New species of Eugerres from the Usumacinta Province, México and Guatemala with a redescription of E. mexicanus (Steindachner, 1863) (Teleostei: Gerreidae)
Fig. 2. a) Graphical index for discrimination of Eugerres castroaguirrei (squares, n = 42) and E. mexicanus (triangles, n = 122), provide by the biplot of second anal-fin spine length against anal-fin base. b) Plot of principal components (PC) scores for E. castroaguirrei (EC) and E. mexicanus (EM) from the southeastern of Mexico and northern Guatemala.
Figure 3 in Colour variations in the European tree frog, Hyla arborea (Linnaeus, 1758), from two small adjacent ponds in the Vojvodina province, Serbia
Figure 3. Two green colour variations: the typical, bright green a) and paler, yellowish b). Photos: Aleksandar Simović.
Figure 1 in Colour variations in the European tree frog, Hyla arborea (Linnaeus, 1758), from two small adjacent ponds in the Vojvodina province, Serbia
Figure 1. Two ponds where the frogs were observed: a) the larger one, near a settlement, overgrown with reeds; b) small, shallow pond with open water. Photos: Sonja Đorđević.
The unpatterned orange morph of Philippine Boiga cynodon photographed in 2016 in the University of the Philipines at Los Baños Quezon Land Grant Forest Reserve, Municipality of Siniloan, Quezon Province, southeastern Luzon Island, Photo: Rafe M. Brown. in Synopsis of the Snakes of the Philippines A Synthesis of Data from Biodiversity Repositories, Field Studies, and the Literature
The unpatterned orange morph of Philippine Boiga cynodon photographed in 2016 in the University of the Philipines at Los Baños Quezon Land Grant Forest Reserve, Municipality of Siniloan, Quezon Province, southeastern Luzon Island, Photo: Rafe M. Brown.
FIGURE 4 in Phylogeography of the banded butterflyfish, Chaetodon striatus, indicates high connectivity between biogeographic provinces and ecosystems in the western Atlantic
FIGURE 4 | Migrate values (number of individuals) and error bars (standard error) of immigration and emigration of individuals of Chaetodon striatus per studied population in the western Atlantic: A. mtDNA concatenated (control region and cyt b) and B. rag 2.
FIGURE 1 in Phylogeography of the banded butterflyfish, Chaetodon striatus, indicates high connectivity between biogeographic provinces and ecosystems in the western Atlantic
FIGURE 1 | Map with all sampling sites along Chaetodon striatus distribution range (red line). Blue color on the map indicates freshwater.
Figure 1 in The influence of land use-impacted tributaries on water quality and phytoplankton in the Mooi River, North West Province, South Africa
Figure 1: Catchment area of the Mooi River from its source to the confluence with the Vaal River, showing the position of sampling sites in the main stream (1–8) and in the tributaries (WFS, GM and WS). Different types of land use activities in the catchment are also indicated on the map.
Figure 3 in The influence of land use-impacted tributaries on water quality and phytoplankton in the Mooi River, North West Province, South Africa
Figure 3: Canonical Correspondence Analysis (CCA) of the physico-chemical environmental variables, natural log of the phytoplankton data, and the different sites located in the Mooi River for 2015.
Plate XXI, Figs I.1–I.6 – Type I (Spain, Cantabrian Cordillera, Palencia province, Río Carrión, Triollo, 1300 m). I.1, nymph, head and pronotum; I.2, tergites of macropterous ♂ nymph, dorsal view; I.3, mediodorsal setation on tergites of nymph, lateral view; I.4, femora of nymph; I.5, paraprocts of nymph; I.6, cerci of nymph, mediodorsal setation, lateral view. in Steps towards a revision of the Perla bipunctata Pictet, 1833 species complex (Plecoptera: Perlidae)
Plate XXI, Figs I.1–I.6 – Type I (Spain, Cantabrian Cordillera, Palencia province, Río Carrión, Triollo, 1300 m). I.1, nymph, head and pronotum; I.2, tergites of macropterous ♂ nymph, dorsal view; I.3, mediodorsal setation on tergites of nymph, lateral view; I.4, femora of nymph; I.5, paraprocts of nymph; I.6, cerci of nymph, mediodorsal setation, lateral view.
Fig. 3 in A new species of Ischnostomiella Krikken, 1978 from the Limpopo Province of South Africa (Scarabaeidae: Cetoniinae, Xiphoscelidini)
Fig. 3 – Distribution range of the three species of Ischnostomiella Krikken, 1978 within the southern African region. (Map: Google Earth Pro with image from Landsat/Copernicus 12/14/2015).
Fig. 1 in A new species of Ischnostomiella Krikken, 1978 from the Limpopo Province of South Africa (Scarabaeidae: Cetoniinae, Xiphoscelidini)
Fig. 1 – Ischnostomiella rudebecki sp. nov., Holotype ♀: A) dorsal habitus; B) ventral habitus; C) lateral habitus; D) clypeus; E) pygidium; F) specimen labels. Photos: John Irish.
Fig. 2 – A in A new species of Ischnostomiella Krikken, 1978 from the Limpopo Province of South Africa (Scarabaeidae: Cetoniinae, Xiphoscelidini)
Fig. 2 – A, dark ♂, Namibia, Karibib; B, brown-orange ♂, ibidem; C, dark ♀, Namibia, Omaruru. I. werneri Beinhundner, 2005: D, Holotype ♂, Botswana, Gweta; E, Paratype ♂, ibidem; F, "allotype" ♀, ibidem.
Figs. 13–18 in Thalassaphorurini (Collembola: Onychiuridae) in Shandong Province, China, with description of two new species
Figs. 13–18. Allonychiurus shandongensis sp. nov. 13. Dorsal chaetotaxy of body; 14. PAO; 15. Labium; 16. Papillae, sensory rods, and sensory clubs of Ant. III sensory organ; 17. Antenna; 18. Chaetotaxy of Abd. I–VI sterna. Scale bars: 0.1 mm (Figs. 13, 17–18), 0.01 mm (Figs. 14–16).
Figs. 1–6 in Thalassaphorurini (Collembola: Onychiuridae) in Shandong Province, China, with description of two new species
Figs. 1–6. Thalassaphorura biquaternata sp. nov. 1. Dorsal chaetotaxy of body; 2. Ventral chaetotaxy of head; 3. Labium; 4. PAO; 5. Papillae, sensory rods, and sensory clubs of Ant. III sensory organ; 6. Chaetotaxy of Abd. II–VI sterna. Scale bars: 0.1 mm (Figs. 1, 2, 6), 0.01 mm (Figs. 3–5).
Figs. 7–12 in Thalassaphorurini (Collembola: Onychiuridae) in Shandong Province, China, with description of two new species
Figs. 7–12. Thalassaphorura biquaternata sp. nov. 7. Antenna; 8. Distal part of leg I; 9. Distal part of leg II; 10. Chaetotaxy of Abd. III–VI terga; 11. Chaetotaxy of Abd. IV–VI sterna; 12. Anal valves. Scale bars: 0.1 mm (Figs. 7, 10–11), 0.01 mm (Figs. 8–9, 12).
Figs. 19–25 in Thalassaphorurini (Collembola: Onychiuridae) in Shandong Province, China, with description of two new species
Figs. 19–25. Allonychiurus shandongensis sp. nov. 19. Dorsal chaetotaxy of head; 20. Ventral chaetotaxy of head; 21. Distal part of leg II; 22. Distal part of leg III; 23. Chaetotaxy of Abd. IV sterna; 24. Anal valves; 25. Central part of Abd. V sternum with female genital plate. Scale bars: 0.1 mm (Figs. 19, 20, 23), 0.01 mm (Figs. 21–22, 24–25).
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.