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Figures 67-70 from: Sohn J-C, Davis DR, Lopez-Vaamonde C (2015) Revision of the genus Philonome Chambers and its proposed reassignment to the family Tineidae (Lepidoptera, Tineoidea). ZooKeys 494: 69-106. https://doi.org/10.3897/zookeys.494.8748
Figures 67-70 - Female genitalia. 67–69 Argyresthia luteella. 67 Ventral view 68 Enlarged view of signum, ventral view 69 anterior view of Fig. 64 70 Elachista albella, ventral view.
Figure 71 from: Sohn J-C, Davis DR, Lopez-Vaamonde C (2015) Revision of the genus Philonome Chambers and its proposed reassignment to the family Tineidae (Lepidoptera, Tineoidea). ZooKeys 494: 69-106. https://doi.org/10.3897/zookeys.494.8748
Figure 71 - A Neighbor-Joining tree, generated under the K2P nucleotide substitution model, for the species of Philonome. Branch lengths represent the number of substitutions per site.
Figures 10-17 from: Sohn J-C, Davis DR, Lopez-Vaamonde C (2015) Revision of the genus Philonome Chambers and its proposed reassignment to the family Tineidae (Lepidoptera, Tineoidea). ZooKeys 494: 69-106. https://doi.org/10.3897/zookeys.494.8748
Figures 10-17 - Adults. 10 Philonome penerivifera, ♀ paratype (3.6 mm) 11 Philonome kawakitai, ♀ holotype (3.8 mm) 12 Philonome rivifera, ♂ lectotype (3.4 mm) 13 Philonome rivifera, ♂ paralectotype (2.8 mm) 14 Philonome sp., CLV105310 (4.1 mm) 15 Philonome spectata, ♀ holotype (2.3 mm) 16 Argyresthia luteella, ♀ holotype (3.4 mm) 17 Elachista dasycara (= Eurynome albella),♀ holotype (4.0 mm). (Forewing lengths in parentheses).
Figure 1 from: Sohn J-C, Davis DR, Lopez-Vaamonde C (2015) Revision of the genus Philonome Chambers and its proposed reassignment to the family Tineidae (Lepidoptera, Tineoidea). ZooKeys 494: 69-106. https://doi.org/10.3897/zookeys.494.8748
Figure 1 - Maximum likelihood phylogeny of Tineidae s. l. extracted from Sohn et al. (2013), based on 27 nuclear genes. Branches in bold indicate the > 70% bootstrapping support from at least one analysis attempted by Sohn et al. (2013). The 'A' in closed circle represents a well-supported subclade of Tineidae in which Philonome clemensella is included.
Figures 57-60 from: Sohn J-C, Davis DR, Lopez-Vaamonde C (2015) Revision of the genus Philonome Chambers and its proposed reassignment to the family Tineidae (Lepidoptera, Tineoidea). ZooKeys 494: 69-106. https://doi.org/10.3897/zookeys.494.8748
Figures 57-60 - Philonome, female genitalia. 57–58 Philonome nigrescens 57 Ventral view 58 Lateral view of segment 8 and sterigma 59–60 Philonome clemensella 59 Ventral view 60 Lateral view of segment 8 and sterigma.
Figures 61-66 from: Sohn J-C, Davis DR, Lopez-Vaamonde C (2015) Revision of the genus Philonome Chambers and its proposed reassignment to the family Tineidae (Lepidoptera, Tineoidea). ZooKeys 494: 69-106. https://doi.org/10.3897/zookeys.494.8748
Figures 61-66 - Philonome, female genitalia. 61–62 Philonome penerivifera 61 Ventral view 62 Lateral view of segment 8 and sterigma 63–64 Philonome kawakitai 63 Ventral view 64 Lateral view 65–66 Philonome rivifera 65 Ventral view 66 Lateral view of segment 8 and sterigma.
Figures 18-20 from: Sohn J-C, Davis DR, Lopez-Vaamonde C (2015) Revision of the genus Philonome Chambers and its proposed reassignment to the family Tineidae (Lepidoptera, Tineoidea). ZooKeys 494: 69-106. https://doi.org/10.3897/zookeys.494.8748
Figures 18-20 - Philonome clemensella, body morphology. 18 Head, frontal view 19 Legs 20 Wing venation.
Figure 4 from: Baldwin CC, Robertson DR (2015) A new, mesophotic Coryphopterus goby (Teleostei, Gobiidae) from the southern Caribbean, with comments on relationships and depth distributions within the genus. ZooKeys 513: 123-142. https://doi.org/10.3897/zookeys.513.9998
Figure 4 - The strict consensus of a maximum parsimony analysis of the COI region of 42 individuals of Coryphopterus and Lophogobius cyprinoides. Fusigobius duospilus and Rhinogobiops nicholsii were outgroups in the analysis. Numbers above branches represent bootstrap support values > 50. Note: Coryphopterus punctipectophorus from the Gulf of Mexico was not available for inclusion in this analysis.
Figure 2 from: Baldwin CC, Robertson DR (2015) A new, mesophotic Coryphopterus goby (Teleostei, Gobiidae) from the southern Caribbean, with comments on relationships and depth distributions within the genus. ZooKeys 513: 123-142. https://doi.org/10.3897/zookeys.513.9998
Figure 2 - Comparison of A Coryphopterus curasub sp. n., holotype, USNM 406373, 33.3 mm SL, and its most similar congener B Coryphopterus dicrus, USNM 413296, 30 mm SL. Note the differences in the shape of the basicaudal pigment marking (with distinct anterior projection in Coryphopterus curasub), body depth (shallower in Coryphopterus curasub), head pigment (absence of a distinct blotch of black pigment immediately posterior to the orbit and presence of a black triangle of pigment beneath the anteroventral portion of orbit in Coryphopterus curasub (present and absent, respectively, in Coryphopterus dicrus), and trunk pigment (blotches predominantly yellow with few melanophores interspersed among them in Coryphopterus curasub vs. blotches predominantly orange/rust with numerous melanophores interspersed among them in Coryphopterus dicrus).
Figure 3 from: Baldwin CC, Robertson DR (2015) A new, mesophotic Coryphopterus goby (Teleostei, Gobiidae) from the southern Caribbean, with comments on relationships and depth distributions within the genus. ZooKeys 513: 123-142. https://doi.org/10.3897/zookeys.513.9998
Figure 3 - Neighbor-joining tree derived from COI sequences for western Atlantic species of Coryphopterus. The tree was rooted on Fusigobius duospilus. Divergence represented by scale bar = 3%. Note: Coryphopterus punctipectophorus from the Gulf of Mexico was not available for inclusion in this analysis.
Figure 1 from: Baldwin CC, Robertson DR (2015) A new, mesophotic Coryphopterus goby (Teleostei, Gobiidae) from the southern Caribbean, with comments on relationships and depth distributions within the genus. ZooKeys 513: 123-142. https://doi.org/10.3897/zookeys.513.9998
Figure 1 - Coryphopterus curasub sp. n., type specimens: A, B USNM 406373, holotype, Smithsonian DNA number CUR 11373, 33.3 mm SL, female – after preservation (A) and before preservation (B) C USNM 431328, Paratype, CUR 14003, 31.0 mm SL, male, before preservation D USNM 430019, Paratype, CUR 13303, 17.5 mm SL, immature, before preservation and clearing and staining. Note that the dark color on the posterior portion of the caudal fin is an artifact of flash photography and does not reflect the existence of dark pigment. Photos by Ian Silver-Gorges (A) and D. R. Robertson and C. C. Baldwin (B–D).
Figure 5 from: Baldwin CC, Robertson DR (2015) A new, mesophotic Coryphopterus goby (Teleostei, Gobiidae) from the southern Caribbean, with comments on relationships and depth distributions within the genus. ZooKeys 513: 123-142. https://doi.org/10.3897/zookeys.513.9998
Figure 5 - Depth ranges for Coryphopterus species. Data are from Böhlke and Robins (1960, 1962); Thacker and Cole (2002); Feitoza et al. (2005); Robertson and Van Tassell (2015); the Florida Museum of Natural History online fish catalog – http://specifyportal.flmnh.ufl.edu/fishes/; the Florida Fish and Wildlife Conservation Commission online catalog http://myfwc.com/research/saltwater/specimen-collections/sis/ichthyology/; the Smithsonian National Museum of Natural History online catalog – www.vertebrates.si.edu//search/fishes); and this study.
Figure 4 from: DeWalt RE, South EJ, Robertson DR, Marburger JE, Smith WW, Brinson V (2016) Mayflies, stoneflies, and caddisflies of streams and marshes of Indiana Dunes National Lakeshore, USA. ZooKeys 556: 43-63. https://doi.org/10.3897/zookeys.556.6725
Figure 4 - Mean ± SE of EPT richness by stream size and waterbody type within Indiana Dunes National Lakeshore and Indiana Dune State Park. Number in bar indicates sample size.
Figure 1 from: DeWalt RE, South EJ, Robertson DR, Marburger JE, Smith WW, Brinson V (2016) Mayflies, stoneflies, and caddisflies of streams and marshes of Indiana Dunes National Lakeshore, USA. ZooKeys 556: 43-63. https://doi.org/10.3897/zookeys.556.6725
Figure 1 - Sampling locations and extent of Indiana Dunes National Lakeshore and Indiana Dunes State Park (INSP). Site numbers in circles are from Table 1.
Figure 3 from: DeWalt RE, South EJ, Robertson DR, Marburger JE, Smith WW, Brinson V (2016) Mayflies, stoneflies, and caddisflies of streams and marshes of Indiana Dunes National Lakeshore, USA. ZooKeys 556: 43-63. https://doi.org/10.3897/zookeys.556.6725
Figure 3 - EPT richness found at each of 19 locations in Indiana Dunes National Lakeshore. Refer to Table 1 for specific site information.
Figure 2 from: DeWalt RE, South EJ, Robertson DR, Marburger JE, Smith WW, Brinson V (2016) Mayflies, stoneflies, and caddisflies of streams and marshes of Indiana Dunes National Lakeshore, USA. ZooKeys 556: 43-63. https://doi.org/10.3897/zookeys.556.6725
Figure 2 - Comparison of caddisfly species richness within families at Indiana Dunes National Lakeshore versus Indiana records published by Rasmussen and Morse (2014).
Figure 8 from: Neild AFE, Nakahara S, Zacca T, Fratello S, Lamas G, Le Crom J-F, Dolibaina DR, Dias FMS, Casagrande MM, Mielke OHH, Espeland M (2015) Two new species of Euptychia Hübner, 1818 from the upper Amazon basin (Lepidoptera, Nymphalidae, Satyrinae). ZooKeys 541: 87-108. https://doi.org/10.3897/zookeys.541.6297
Figure 8 - Euptychia sophiae sp. n. Genitalia of paratype male: a dorsal view b ventral view c lateral view ("G" indicates fused gnathos) d aedeagus, dorsal and e lateral views. DZUP collection. Photos by Diego R. Dolibaina. Scale bar: 0.5 mm.
Figure 7 from: Neild AFE, Nakahara S, Zacca T, Fratello S, Lamas G, Le Crom J-F, Dolibaina DR, Dias FMS, Casagrande MM, Mielke OHH, Espeland M (2015) Two new species of Euptychia Hübner, 1818 from the upper Amazon basin (Lepidoptera, Nymphalidae, Satyrinae). ZooKeys 541: 87-108. https://doi.org/10.3897/zookeys.541.6297
Figure 7 - Euptychia sophiae sp. n. holotype male, dorsal (left) and ventral (right). FW length: 18.0 mm. DZUP collection. Photos by Thamara Zacca. Scale bar: 10 mm.
Map 1 from: Neild AFE, Nakahara S, Zacca T, Fratello S, Lamas G, Le Crom J-F, Dolibaina DR, Dias FMS, Casagrande MM, Mielke OHH, Espeland M (2015) Two new species of Euptychia Hübner, 1818 from the upper Amazon basin (Lepidoptera, Nymphalidae, Satyrinae). ZooKeys 541: 87-108. https://doi.org/10.3897/zookeys.541.6297
Map 1 - Distribution of Euptychia attenboroughi sp. n. (blue circles) and Euptychia sophiae sp. n. (green squares).
Figure 6 from: Neild AFE, Nakahara S, Zacca T, Fratello S, Lamas G, Le Crom J-F, Dolibaina DR, Dias FMS, Casagrande MM, Mielke OHH, Espeland M (2015) Two new species of Euptychia Hübner, 1818 from the upper Amazon basin (Lepidoptera, Nymphalidae, Satyrinae). ZooKeys 541: 87-108. https://doi.org/10.3897/zookeys.541.6297
Figure 6 - Euptychia attenboroughi sp. n. Genitalia of paratype female: postero-ventral view. AN collection. Photos by Andrew Neild. Scale bar: 0.5 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)
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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.