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Fig. 1 in Surprising genomic diversity in the Neotropical fish Synbranchus marmoratus (Teleostei: Synbranchidae): how many species?
Fig. 1. South America map showing the major river drainages. The detail show the collecting locations. The bold dashed line in the detail indicates the limit of the last great marine incursion into South America (from the south) at approximately five million years ago (modified from Frailey, 2002). The lighter dashed lines indicate the state-specific boundaries hosting the collecting locations. MS 1,2 = rio Miranda (state of Mato Grosso do Sul; 2n=46 and 2n=42); SP 1 = rio Mogi-Guaçu (state of São Paulo; 2n=44); SP 2 = rio Tietê (state of São Paulo; 2n=42); SP 3 = rio Paraná (state of São Paulo; 2n=42); PR 1 = ribeirão Água do Caixão (state of Paraná; 2n=46); PR = rio Tibagi (state of Paraná; 2n=42); PR = rio Paraná (state of Paraná; 2n=42).
Figure 33 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 33. Cyphophthalmus hlavaci sp. nov. (holotype). A, spermatopositor (dorsal view); B, ventral prosomal complex; C, basitarsus and telotarsus of leg I; D, basitarsus and telotarsus of leg IV; E, tibia and tarsus of pedipalp; F, chelicera; G, adenostyle. Scale bars: A, G = 100 Mm; B–F = 400 Mm.
Figure 28 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 28. Cyphophthalmus rumijae sp. nov. (A, C, F – holotype, B – female paratype, D–E – male paratype). A, male dorsum; B, female dorsum; C, dorsum granulation (fifth to ninth tergite); D, detail of granulation (convex tubercles) at the border of eighth to ninth tergite; E, terminal posterior part of the male dorsum with pores of anal glands; F, dorsum, frontal view.
Figure 25 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 25. Cyphophthalmus martensi sp. nov. (holotype). A, spermatopositor (dorsal view); B, ventral prosomal complex; C, basitarsus and telotarsus of leg I; D, basitarsus and telotarsus of leg IV; E, tibia and tarsus of pedipalp; F, chelicera; G, adenostyle. Scale bars: A, G = 100 Mm; B–F = 400 Mm.
Figure 36 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 36. Distribution of presented Cyphophthalmus species in the Dinaric Alps. A, troglobite; B, endogean.
Figure 24 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 24. Cyphophthalmus ognjenovici sp. nov. (A, F – holotype, B–D – female paratype, E – male paratype). A, male dorsum; B, female dorsum; C, dorsum granulation (fifth to ninth tergite); D, detail of granulation (convex tubercles) at the border of eighth to ninth tergite; E, terminal posterior part of the male dorsum with pores of anal glands; F, dorsum, frontal view.
Figure 22 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 22. Cyphophthalmus trebinjanus sp. nov. (A – holotype, B–D, F – female paratype, E – male paratype). A, male dorsum; B, female dorsum; C, dorsum granulation (fifth to ninth tergite); D, detail of granulation (convex tubercles) at the border of eighth to ninth tergite; E, terminal posterior part of the male dorsum with pores of anal glands; F, dorsum, frontal view.
Figure 20 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 20. Cyphophthalmus conocephalus sp. nov. (holotype). A, male dorsum; B, anterior margin of dorsum (dorsal view); C, dorsum granulation (fifth to ninth tergite); D, detail of granulation (convex tubercles) at the border of eighth to ninth tergite; E, terminal posterior part of the male dorsum with pores of anal glands; F, dorsum, frontal view.
Figure 19 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 19. Cyphophthalmus conocephalus sp. nov. (holotype). A, spermatopositor (dorsal view); B, ventral prosomal complex; C, basitarsus and telotarsus of leg I; D, basitarsus and telotarsus of leg IV; E, tibia and tarsus of pedipalp; F, chelicera; G, adenostyle. Scale bars: A, G = 100 Mm; B–F = 400 Mm.
Figure 30 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 30. Cyphophthalmus corfuanus (Kratochvíl) (Corfu). A, male dorsum; B, female dorsum; C, dorsum granulation (fifth to ninth tergite); D, detail of granulation (convex tubercles) at the border of eighth to ninth tergite; E, dorsum, frontal view; F, terminal posterior part of the male dorsum with pores of anal glands.
Figure 15 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 15. Cyphophthalmus neretvanus sp. nov. (holotype). A, spermatopositor (dorsal view); B, ventral prosomal complex; C, basitarsus and telotarsus of leg I; D, basitarsus and telotarsus of leg IV; E, tibia and tarsus of pedipalp; F, chelicera; G, adenostyle. Scale bars: A, G = 100 Mm; B–F = 400 Mm.
Figure 17 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 17. Cyphophthalmus kratochvili sp. nov. (holotype). A, spermatopositor (dorsal view); B, ventral prosomal complex; C, basitarsus and telotarsus of leg I; D, basitarsus and telotarsus of leg IV; E, tibia and tarsus of pedipalp; F, chelicera; G, adenostyle. Scale bars: A, G = 100 Mm; B–F = 400 Mm.
Figure 32 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 32. Cyphophthalmus zetae sp. nov. (A, C, D, F – holotype, B – female paratype, E – male paratype). A, male dorsum; B, female dorsum; C, dorsum granulation (fifth to ninth tergite); D, detail of granulation (convex tubercles) at the border of eighth to ninth tergite; E, terminal posterior part of the male dorsum with pores of anal glands; F, dorsum, frontal view.
Figure 13 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 13. Cyphophthalmus gordani sp. nov. (holotype). A, spermatopositor (dorsal view); B, ventral prosomal complex; C, basitarsus and telotarsus of leg I; D, basitarsus and telotarsus of leg IV; E, tibia and tarsus of pedipalp; F, chelicera; G, adenostyle. Scale bars: A, G = 100 Mm; B–F = 400 Mm.
Figure 16 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 16. Cyphophthalmus neretvanus sp. nov. (A, F – holotype, B–D – female paratype, E – male paratype). A, male dorsum; B, female dorsum; C, dorsum granulation (fifth to ninth tergite); D, detail of granulation (convex tubercles) at the border of eighth to ninth tergite; E, terminal posterior part of the male dorsum with pores of anal glands; F, dorsum, frontal view.
Figure 26 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 26. Cyphophthalmus martensi sp. nov. (paratypes from Žanjica). A, male dorsum; B, female dorsum; C, dorsum granulation (fifth to ninth tergite); D, detail of granulation (convex tubercles) at the border of eighth to ninth tergite; E, terminal posterior part of the male dorsum with pores of anal glands; F, dorsum, frontal view.
Figure 31 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 31. Cyphophthalmus zetae sp. nov. (holotype). A, spermatopositor (dorsal view); B, ventral prosomal complex; C, basitarsus and telotarsus of leg I; D, basitarsus and telotarsus of leg IV; E, tibia and tarsus of pedipalp; F, chelicera; G, adenostyle. Scale bars: A, G = 100 Mm; B–F = 400 Mm.
Figure 10 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 10. Cyphophthalmus thracicus sp. nov. (holotype except B, F – female paratype). A, male dorsum; B, female dorsum; C, dorsum granulation (fifth to ninth tergite); D, detail of granulation (convex tubercles) at the border of eighth to ninth tergite; E, terminal posterior part of the male dorsum with pores of anal glands; F, dorsum, frontal view.
Figure 9 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 9. Cyphophthalmus thracicus sp. nov. (holotype). A, spermatopositor (dorsal view); B, ventral prosomal complex; C, basitarsus and telotarsus of leg I; D, basitarsus and telotarsus of leg IV; E, tibia and tarsus of pedipalp; F, chelicera; G, adenostyle. Scale bars: A, G = 100 Mm; B–F = 400 Mm.
Figure 8 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 8. Cyphophthalmus paragamiani sp. nov. (holotype except B, D – female paratype). A, male dorsum; B, female dorsum (partially damaged); C, dorsum granulation (fifth to ninth tergite); D, detail of granulation (convex tubercles) at the border of eighth to ninth tergite; E, terminal posterior part of the male dorsum with pores of anal glands; F, dorsum, frontal view.
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.