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Figure 3 in Molecular phylogeny, analysis of character evolution, and submersible collections enable a new classification of a diverse group of gobies (Teleostei: Gobiidae: Nes subgroup), including nine new species and four new genera
Figure 3. Examples of papillae patterns in which rows 5i and 5s are connected (A–C) or distinctly separate (D–F). (A) Varicus bucca, UMML 7119; (B) Pinnichthys prolata, AMNH 87272; (C) Psilotris celsa, USNM 98429; (D) Chriolepis minutilla, USNM 322595; (E) Chriolepis zebra, CAS 31001; (F) Gobulus crescentalis, USNM 48258.
Figure 4 in Molecular phylogeny, analysis of character evolution, and submersible collections enable a new classification of a diverse group of gobies (Teleostei: Gobiidae: Nes subgroup), including nine new species and four new genera
Figure 4. Variation in branching pattern of pelvic rays 1–4 in the Nes subgroup. (A) branched but united at tips as a flattened, spatulate fleshy pad, Varicus adamsi, USNM 220985; (B) branched to the tips, some branches with minute fleshy tips, Varicus vespa, paratype (USNM 221524); (C) rays unbranched, or branched internally and re-fused (as in ray 3), tips with fleshy pads, Varicus bucca, holotype ANSP 93083; (D) rays branched, mostly internally and re-fused, tips with fleshy pads, Varicus sp., USNM 199060; (E) all rays unbranched without fleshy tips, Varicus veliguttatus USNM 220982; (F) all rays branched, not re-fused and no fleshy tips, Psilotris boehlkei, USNM 427234.
Figure 2 in Molecular phylogeny, analysis of character evolution, and submersible collections enable a new classification of a diverse group of gobies (Teleostei: Gobiidae: Nes subgroup), including nine new species and four new genera
Figure 2. Anal-fin pterygiophore insertion patterns. (A) One anal-fin pterygiophore inserted anterior to first haemal spine (Varicus cephalocellatus paratype, USNM 427227); (B) rare pattern in which haemal spine on vertebra 12 is reduced, and first elongate haemal spine appears on vertebra 13, giving the appearance of two anal-pterygiophores inserted before first haemal spine. This pattern is considered homologous to pattern depicted in A, and occurs only in species in which the pattern from A is also observed (Varicus cephalocellatus paratype, USNM 427227); (C) two anal-fin pterygiophores inserted anterior to first haemal spine (Chriolepis lepidota holotype USNM 211456).
Figure 5 in Molecular phylogeny, analysis of character evolution, and submersible collections enable a new classification of a diverse group of gobies (Teleostei: Gobiidae: Nes subgroup), including nine new species and four new genera
Figure 5. Bayesian phylogeny from MrBayes analysis of the Gobiosomatini. Tip labels follow classification recognized prior to this study. Red bars indicate new classification from this study (Table 2). Support values at nodes are Bayesian posterior probabilities. The "?" for Chriolepis cf. fisheri refers to the incertae sedis status of this species (see "Remarks" section for Chriolepis). Species from the eastern Pacific are denoted with "(P)".
Figure 30. Varicus cephalocellatus papillae pattern, drawn from paratype USNM 426788 in Molecular phylogeny, analysis of character evolution, and submersible collections enable a new classification of a diverse group of gobies (Teleostei: Gobiidae: Nes subgroup), including nine new species and four new genera
Figure 30. Varicus cephalocellatus papillae pattern, drawn from paratype USNM 426788. Illustration by J.L. Van Tassell. Note that two paratypes USNM 427227 have papillae rows 5i and 5s separated by the space of 1 or two papillae.
Figure 11 in Molecular phylogeny, analysis of character evolution, and submersible collections enable a new classification of a diverse group of gobies (Teleostei: Gobiidae: Nes subgroup), including nine new species and four new genera
Figure 11. Pinnichthys aimoriensis in preservation. (A) holotype, 22.4 mm SL, CIUFES 2414; (B) paratype, 16.4 mm SL, AMNH 265021. Photos by J.L. Van Tassell.
Figure 18 in Molecular phylogeny, analysis of character evolution, and submersible collections enable a new classification of a diverse group of gobies (Teleostei: Gobiidae: Nes subgroup), including nine new species and four new genera
Figure 18. Psilotris laetarii holotype, preserved, 23.6 mm SL, AMNH 261272. Photo by J.L. Van Tassell.
Figure 10 in Molecular phylogeny, analysis of character evolution, and submersible collections enable a new classification of a diverse group of gobies (Teleostei: Gobiidae: Nes subgroup), including nine new species and four new genera
Figure 10. Pinnichthys aimoriensis holotype, prior to preservation, 22.4 mm SL, CIUFES 2414. Photo by Hudson Pinheiro.
Figure 27 in Molecular phylogeny, analysis of character evolution, and submersible collections enable a new classification of a diverse group of gobies (Teleostei: Gobiidae: Nes subgroup), including nine new species and four new genera
Figure 27. Varicus cephalocellatus, illustration of holotype, 28.2 mm SL, USNM 427232, based on notes of live coloration, by R.G. Gilmore.
Figure 21 in Molecular phylogeny, analysis of character evolution, and submersible collections enable a new classification of a diverse group of gobies (Teleostei: Gobiidae: Nes subgroup), including nine new species and four new genera
Figure 21. Psilotris laurae holotype, preserved, 26.8 mm SL, USNM 426779. Photo by J.L. Van Tassell.
Figure 8 in Molecular phylogeny, analysis of character evolution, and submersible collections enable a new classification of a diverse group of gobies (Teleostei: Gobiidae: Nes subgroup), including nine new species and four new genera
Figure 8. Ancestral character estimation for (A) branched versus unbranched 5th pelvic ray and (B) presence/absence of a well-developed membrane connecting the innermost pelvic rays. Pies at nodes represent posterior probabilities for ancestor's character state. Species from the eastern Pacific are denoted with "(P)".
Figure 26 in Molecular phylogeny, analysis of character evolution, and submersible collections enable a new classification of a diverse group of gobies (Teleostei: Gobiidae: Nes subgroup), including nine new species and four new genera
Figure 26. Varicus adamsi papillae pattern, composite from type series. Illustration by J.L. Van Tassell.
Figure 14. Pinnichthys saurimimica, holotype. 55.5 in Molecular phylogeny, analysis of character evolution, and submersible collections enable a new classification of a diverse group of gobies (Teleostei: Gobiidae: Nes subgroup), including nine new species and four new genera
Figure 14. Pinnichthys saurimimica, holotype. 55.5 mm SL, USNM 427228, in situ at 282 m, Bahamas, photo by R.G. Gilmore, from the Johnson Sea Link II submersible.
Figure 15. Pinnichthys saurimimica holotype, 55.4 in Molecular phylogeny, analysis of character evolution, and submersible collections enable a new classification of a diverse group of gobies (Teleostei: Gobiidae: Nes subgroup), including nine new species and four new genera
Figure 15. Pinnichthys saurimimica holotype, 55.4 mm SL, USNM 427228, preserved. Photo by J.L. Van Tassell.
Figure 83 in Previously undocumented diversity and abundance of cryptic species: a phylogenetic analysis of Indo-Pacific Arminidae Rafinesque, 1814 (Mollusca: Nudibranchia) with descriptions of 20 new species of Dermatobranchus
Figure 83. Dermatobranchus tuberculatus sp. nov. Buccal armature, CASIZ 112297, Ligpo Island, Balayan Bay, Luzon, Philippines. A, jaw; B, masticatory margin; C, entire radula; D, half-row of radular teeth; E, central portion of radula.
Figure 80 in Previously undocumented diversity and abundance of cryptic species: a phylogenetic analysis of Indo-Pacific Arminidae Rafinesque, 1814 (Mollusca: Nudibranchia) with descriptions of 20 new species of Dermatobranchus
Figure 80. Dermatobranchus semilunus sp. nov. Buccal armature, CASIZ 110407, Cabilao, Bohol, Philippines. A, jaws; B, masticatory margin; C, half-row of radular teeth; D, central portion of radula; E, middle lateral teeth; F, outer lateral teeth.
Figure 77 in Previously undocumented diversity and abundance of cryptic species: a phylogenetic analysis of Indo-Pacific Arminidae Rafinesque, 1814 (Mollusca: Nudibranchia) with descriptions of 20 new species of Dermatobranchus
Figure 77. Dermatobranchus rodmani sp. nov. Reproductive system, CASIZ 173400, Radama Islands, Madagascar. a, ampulla; bc, bursa copulatrix; fg, female gland mass; p, penis; pr, prostate; v, vagina; vd, vaginal duct. Scale bar = 0.37 mm.
Figure 76 in Previously undocumented diversity and abundance of cryptic species: a phylogenetic analysis of Indo-Pacific Arminidae Rafinesque, 1814 (Mollusca: Nudibranchia) with descriptions of 20 new species of Dermatobranchus
Figure 76. Dermatobranchus rodmani sp. nov. Buccal armature, CASIZ 174170, Pulau Labus. Tioman, Malaysia. A, jaws; B, masticatory margin; C, central portion of radula; D, outer radular teeth.
Figure 74. Living animals. A in Previously undocumented diversity and abundance of cryptic species: a phylogenetic analysis of Indo-Pacific Arminidae Rafinesque, 1814 (Mollusca: Nudibranchia) with descriptions of 20 new species of Dermatobranchus
Figure 74. Living animals. A, Dermatobranchus rodmani sp. nov., CASIZ 173400, Radama Islands, Madagascar, photo by T. M. Gosliner. B, Dermatobranchus rodmani sp. nov., CASIZ 174170, Pulau Labus, Malaysia, photo by D. W. Behrens. C, Dermatobranchus semilunus sp. nov., Pulau Chimbe, off Tioman, Malaysia, photo by T. M. Gosliner. D, Dermatobranchus semilunus sp. nov., CASIZ 073045, Madang, Papua New Guinea, photo by T. M. Gosliner. E, Dermatobranchus semilunus sp. nov., CASIZ 110407, Cabilao, Bohol, Philippines, photo by T. M. Gosliner. F, Dermatobranchus tuberculatus sp. nov., CASIZ 110361, Ligpo Island, Luzon, Philippines, photo by T. M. Gosliner. G, Dermatobranchus tuberculatus sp. nov., CASIZ 096332, Devil's Point, Maricaban Island, Luzon, Philippines, photo by T. M. Gosliner. H, Dermatobranchus tuberculatus sp. nov., CASIZ 174171, Pulau Tenggol, Malaysia, photo by T. M. Gosliner.
Figure 72 in Previously undocumented diversity and abundance of cryptic species: a phylogenetic analysis of Indo-Pacific Arminidae Rafinesque, 1814 (Mollusca: Nudibranchia) with descriptions of 20 new species of Dermatobranchus
Figure 72. Dermatobranchus piperoides sp. nov. Buccal armature, CASIZ 174169, St Leu, Reunion Island. A, jaw; B, masticatory margin; C, D, central portion of radula; E, F, half-row of teeth.
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.