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FIGURE 4 in Diogenidae) described from laboratory reared material
FIGURE 4. Areopaguristes japonicus (Miyake, 1961), megalopa: A, lateral view; B, antennule; C, antenna; D, mandibles; E, maxillule; F; maxilla; G, first maxilliped; H, second maxilliped; I; third maxilliped. Scale bars = 0.5 mm (A), 0.1 mm (B–I).
Figure 5. Fouldenia cranial material I in Styracopterid (Actinopterygii) ontogeny and the multiple origins of post-Hangenberg deep-bodied fishes
Figure 5. Fouldenia cranial material I. Photographs and interpretative drawings for specimens of 4–8 cm in total length. Unlabelled scale bars equal 1 cm. Medium-grey infill indicates the extent of thick ganoine ornament. Light-grey infill indicates unidentified skull material. A, NMS 1980.40.30; B, NHM P14562; C, NMS 1965.4.3; D, NMS 1956.5.1; E, NMS 1984.67.61; F, NHM P13179; G, NHM P13180; H, NHM P61546.
FIGURE 6 in Morphometric and morphological variation in Myotis simus Thomas (Chiroptera, Vespertilionidae), with an appraisal of the identity of Myotis guaycuru Proença based on the analysis of the type material
FIGURE 6. Dorsal view of the skulls of two specimens of M. simus: A―from Santa Cruz, Bolivia (USNM 584502), B―from Pasco, Peru (USNM 364482). Scale bar = 5 mm.
FIGURE 2 in Morphometric and morphological variation in Myotis simus Thomas (Chiroptera, Vespertilionidae), with an appraisal of the identity of Myotis guaycuru Proença based on the analysis of the type material
FIGURE 2. Body (in fluid) of the holotype of M. guaycuru (ALP 9277). Scale bar = 10 mm. Bellow on the left, the arrow shows the plagiopatagium attachment.
FIGURE 1 in Morphometric and morphological variation in Myotis simus Thomas (Chiroptera, Vespertilionidae), with an appraisal of the identity of Myotis guaycuru Proença based on the analysis of the type material
FIGURE 1. Geographic mapping of samples analyzed in the present study: (1) Cercado, Beni, Bolivia; (2) Borba, Amazonas, Brazil; (3) Manaus, Amazonas, Brazil; (4) Parintins, Amazonas, Brazil; (5) El Refugio, Santa Cruz, Bolivia; (6) Salobra, Mato Grosso do Sul, Brazil (type specimen of M. guaycuru) (7) Rio Juruá, Amazonas, Brazil; (8) Ucayali, Loreto, Peru; and (9) San Juan, Pasco, Peru.
FIGURE 4 in Morphometric and morphological variation in Myotis simus Thomas (Chiroptera, Vespertilionidae), with an appraisal of the identity of Myotis guaycuru Proença based on the analysis of the type material
FIGURE 4. Left (a): Multivariate individual scores of data in the two first principal components for samples of M. simus labeled by locality — (1) Cercado, Beni, Bolivia; (2) Borba, Amazonas, Brazil; (3) Manaus, Amazonas, Brazil; (4) Parintins, Amazonas, Brazil; (5) El Refugio, Santa Cruz, Bolivia; (6) Salobra, Mato Grosso do Sul, Brazil (type specimen of M. guaycuru) (7) Rio Juruá, Amazonas, Brazil; (8) Ucayali, Loreto, Peru; and (9) San Juan, Pasco, Peru. Right (b): Corresponding vector correlations (greater than 0.29) of craniometric characters with the first two eigenvectors.
FIGURE 7 in Morphometric and morphological variation in Myotis simus Thomas (Chiroptera, Vespertilionidae), with an appraisal of the identity of Myotis guaycuru Proença based on the analysis of the type material
FIGURE 7. Dorsal, lateral and ventral views of the skull and mandible of the holotype of M. simus (BMNH 85.5.12.2). Scale bar = 5 mm. Photographs provided by Roberto Portela Miguez (The Natural History Museum, England).
FIGURE 3 in Morphometric and morphological variation in Myotis simus Thomas (Chiroptera, Vespertilionidae), with an appraisal of the identity of Myotis guaycuru Proença based on the analysis of the type material
FIGURE 3. Dorsal, lateral and ventral views of the skull and mandible of the holotype of M. guaycuru (ALP 9277). Scale bar = 5 mm. The distance between the dentary bones is reduced due to the disarticulation of the mandibular symphysis.
Supplementary material 1 from: van Deurs M, Moran NP, Schreiber Plet-Hansen K, Dinesen GE, Azour F, Carl H, Møller PR, Behrens JW (2021) Impacts of the invasive round goby (Neogobius melanostomus) on benthic invertebrate fauna: a case study from the Baltic Sea. NeoBiota 68: 19-30. https://doi.org/10.3897/neobiota.68.67340
S1. Sampling Areas (Figure S1); S2. Taxonomic Groupings S1; S3. Model Specifications (Table S2); S4. Sensitivity Analyses (Table S3, Figure S2)
Data underlying RSOS-210474: Mitochondrial DNA sequencing of a wet-collection syntype demonstrates the importance of type material as genetic resource for Lantern Shark taxonomy (Chondrichthyes: Etmopteridae)
<p>After initial detection of target archival DNA of a 116 year old syntype specimen of the Smooth Lanternshark, <i>Etmopterus pusillus</i> in a single stranded DNA library, we shotgun-sequenced additional 9 million reads from this same DNA library. Sequencing reads were used for extracting mitochondrial sequence information for analyses of mitochondrial DNA characteristics and reconstruction of the mitochondrial genome. The archival DNA is highly fragmented. A total of 4,599 mitochondrial reads were available for the genome reconstruction using an iterative mapping approach. The resulting genome sequence has a 12 times coverage and a length of 16,741 basepairs. All 37 vertebrate mitochondrial loci plus the control region were identified and annotated. The mitochondrial NADH2 gene was subsequently used to place the syntype haplotype in a network comprising multiple <i>E. pusillus</i> samples from various distant localities as well as sequences from a morphological similar species, the Shortfin Smooth Lantern Shark <i>Etmopterus joungi</i>. Results confirm the almost global distribution of <i>E. pusillus</i> and suggest <i>E. joungi </i>to be a junior synonym of <i>E. pusillus</i>. As mitochondrial DNA often represents the only available reference information in non-model organisms, this study illustrates the importance of mitochondrial DNA from an aged, wet-collection type specimen for taxonomy.</p>
FIG. 7 in The zoeal development of Nanocassiope granulipes (Sakai, 1939) (Crustacea: Decapoda: Brachyura: Xanthidae) described from laboratory-reared material
FIG. 7. Nanocassiope granulipes (Sakai, 1939). Maxilla: (a) Žrst zoea; (b) second zoea; (c) third zoea; (d) fourth zoea.
FIG. 12 in The zoeal development of Nanocassiope granulipes (Sakai, 1939) (Crustacea: Decapoda: Brachyura: Xanthidae) described from laboratory-reared material
FIG. 12. Nanocassiope granulipes (Sakai, 1939). Lateral view of abdomen: (a) Žrst zoea; (b) second zoea; (c) third zoea; (d) fourth zoea.
FIG. 9 in The zoeal development of Nanocassiope granulipes (Sakai, 1939) (Crustacea: Decapoda: Brachyura: Xanthidae) described from laboratory-reared material
FIG. 9. Nanocassiope granulipes (Sakai, 1939). Second maxilliped: (a) Žrst zoea; (b) second zoea; (c) third zoea; (d) fourth zoea.
FIG. 6 in The zoeal development of Nanocassiope granulipes (Sakai, 1939) (Crustacea: Decapoda: Brachyura: Xanthidae) described from laboratory-reared material
FIG. 6. Nanocassiope granulipes (Sakai, 1939). Maxillule: (a) Žrst zoea; (b) second zoea; (c) third zoea; (d) fourth zoea.
FIG. 2 in The zoeal development of Nanocassiope granulipes (Sakai, 1939) (Crustacea: Decapoda: Brachyura: Xanthidae) described from laboratory-reared material
FIG. 2. Nanocassiope granulipes (Sakai, 1939). Anterior view of carapace: (a) third zoea; (b) fourth zoea.
FIG. 8 in The zoeal development of Nanocassiope granulipes (Sakai, 1939) (Crustacea: Decapoda: Brachyura: Xanthidae) described from laboratory-reared material
FIG. 8. Nanocassiope granulipes (Sakai, 1939). First maxilliped: (a) Žrst zoea; (b) second zoea; (c) third zoea; (d) fourth zoea.
FIG. 13 in The zoeal development of Nanocassiope granulipes (Sakai, 1939) (Crustacea: Decapoda: Brachyura: Xanthidae) described from laboratory-reared material
FIG. 13. Nanocassiope granulipes (Sakai, 1939). Dorsal view of telson: (a) Žrst zoea; (b) second zoea; (c) third zoea; (d) fourth zoea.
FIG. 5 in The zoeal development of Nanocassiope granulipes (Sakai, 1939) (Crustacea: Decapoda: Brachyura: Xanthidae) described from laboratory-reared material
FIG. 5. Nanocassiope granulipes (Sakai, 1939). Antenna: (a) Žrst zoea; (c) second zoea; (e) third zoea; (g) fourth zoea. Antennal exopod: (b) Žrst zoea; (d) second zoea; (f) third zoea; (h) fourth zoea.
FIGURE 2 in Review of Sebadexius Ledoyer, 1984 (Amphipoda, Dexaminidae, Dexamininae) based on new material from The Philippines, with Sebadexius cebuense sp. nov.
FIGURE 2. Sebadexius cebuense sp. nov. Holotype, female. gp2, gnathopod 2; p3–7, pereopods 3 to 7; arrow points to enlarged hollow-tipped seta.
FIGURE 9 in Mysidae (Mysida) of New Zealand; a checklist, identification key to species and an overview of material in New Zealand collections
FIGURE 9. Uropods, illustrating the relative lengths of exo- and endopods. a, Tenagomysis robusta Tattersall, 1923; b, T. similis Tattersall, 1923 (after Tattersall 1923).
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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.