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Fig. 12. A. Climacia antillana Alayo, 1968 in Taxonomic revision and first phylogeny of Climacia McLachlan, 1869 (Neuroptera: Sisyridae), with new species and identification key
Fig. 12. A. Climacia antillana Alayo, 1968: A, Distribution map.
Fig. 6 in Taxonomic revision and first phylogeny of Climacia McLachlan, 1869 (Neuroptera: Sisyridae), with new species and identification key
Fig. 6. Climacia McLachlan distribution map with focus on Nearctic and Neotropical regions.
Figure 5 from: dos Santos SA, de Britto MR (2021) The ichthyofauna of a poorly known area in the middle-southern Espinhaço mountain range, state of Minas Gerais, Brazil: diagnostics and identification keys. ZooKeys 1054: 25-66. https://doi.org/10.3897/zookeys.1054.67554
Figure 5 Fish species from the middle-southern Espinhaço mountain range, Minas Gerais state, Brazil AGymnotiformes (Gymnotus carapo group, MNRJ 48407, 130.5 mm SL) BSynbranchiformes (Synbranchus marmoratus group, MNRJ 48448, 116.8 mm SL) CCyprinodontiformes (Phalloceros uai, MNRJ 48408, 32.0 mm (female – above) and 16.3 mm (male – below) SL) DCichliformes (Australoheros mattosi, MNRJ 48454, 54.6 mm SL ECichliformes (Australoheros sp., MNRJ 46859, 39.3 mm SL).
Figure 4 from: dos Santos SA, de Britto MR (2021) The ichthyofauna of a poorly known area in the middle-southern Espinhaço mountain range, state of Minas Gerais, Brazil: diagnostics and identification keys. ZooKeys 1054: 25-66. https://doi.org/10.3897/zookeys.1054.67554
Figure 4 Siluriformes species from the middle-southern Espinhaço mountain range, Minas Gerais state, Brazil ABunocephalus hartti, MZUSP 064227, 44.7 BTrichomycterus melanopygius, MNRJ 47902, 85.2 mm SL CTrichomycterus sp. A, MNRJ 47901, 87.4 mm SL DTrichomycterus sp. B, MNRJ 46932, 57.0 mm SL ECallichthys callichthys, MNRJ 48501, 58.2 mm SL FEuryochus thysanos, MNRJ 47897, 74.4 mm SL GHarttia intermontana, MNRJ 48463, 42.4 mm SL HHypostomus francisci, MZUSP 37162, 66.8 mm SL INeoplecostomus sp. A, MNRJ 46935, 73.0 mm SL JNeoplecostomus sp. B, MNRJ 48431, 43.0 mm SL KPareiorhaphis scutula, MNRJ 48471, 88.1 mm SL LPareiorhaphis vetula, MNRJ 46936, 40.4 mm SL.
Figure 3 from: dos Santos SA, de Britto MR (2021) The ichthyofauna of a poorly known area in the middle-southern Espinhaço mountain range, state of Minas Gerais, Brazil: diagnostics and identification keys. ZooKeys 1054: 25-66. https://doi.org/10.3897/zookeys.1054.67554
Figure 3 Characiformes species from the middle-southern Espinhaço mountain range, Minas Gerais state, Brazil AHypomasticus thayeri, MNRJ 43577, 91.1 mm SL BCharacidium fasciatum, MNRJ 48435, 68.8 mm SL CCharacidium sp. A, MNRJ 46861, 65.5 mm SL DCharacidium sp. B, MNRJ 48460, 56.2 mm SL ECharacidium sp. C, MNRJ 46911, 42.3 mm SL FAstyanax lacustris, MNRJ 48521, 52.6 mm SL GDeuterodon giton, MNRJ 48129, 47.5 mm SL HDeuterodon intermedius, MNRJ 47840, 42.1 mm SL IDeuterodon pedri, MNRJ 48381, 65.5 mm SL JDeuterodon aff. taeniatus, MNRJ 45824, 55.5 mm SL KHasemania nana, MNRJ 48440, 28.4 mm SL LHasemania sp., MNRJ 48416, 25.1 mm SL MOligosarcus argenteus, MNRJ 48393, 82.6 mm SL NPiabina argentea, MZUSP 110200, 44.2 mm SL OPsalidodon rivularis, MNRJ 48516, 46.8 mm SL PPsalidodon sp. MNRJ 48128, 59.4 mm SL QHoplias intermediusMZUSP 54696, 40.4 mm SL.
Figure 7 from: Betters MJ, Cordes EE (2024) New records of Provanna (Gastropoda, Provannidae) from the Costa Rica Margin and an identification key for the genus. ZooKeys 1189: 1-32. https://doi.org/10.3897/zookeys.1189.109734
Figure 7 Bayesian topology of Abyssochrysoid gastropod mollusks A topology based on a 449 bp region of the mitochondrial CO1 gene. Topology was inferred using the HKY+G+I substitution model B topology based on a 266 bp region of the nuclear H3 gene. Novel sequences are bolded and highlighted in yellow. Numbers above branch nodes represent Bayesian posterior probabilities. Numbers below branch nodes represent the proportion of replicate trees in which the associated taxa clustered together in the bootstrap test (10,000 replicates). Only values above 50% are shown. The tree is drawn to scale, with branch lengths representing the number of base substitutions accumulated over time.
Figure 5 from: Betters MJ, Cordes EE (2024) New records of Provanna (Gastropoda, Provannidae) from the Costa Rica Margin and an identification key for the genus. ZooKeys 1189: 1-32. https://doi.org/10.3897/zookeys.1189.109734
Figure 5 Representative radulae of Costa Rican Provanna species AP. laevis from mussel shells BP. laevis from unknown substrate CP. ios from mussel shells DP. ios from unknown substrate E, FP. pacifica from wood. Scale bars: 20 µm (F); 30 µm (E); 40 µm (C); 50 µm (A, B, D).
Figure 4 from: Betters MJ, Cordes EE (2024) New records of Provanna (Gastropoda, Provannidae) from the Costa Rica Margin and an identification key for the genus. ZooKeys 1189: 1-32. https://doi.org/10.3897/zookeys.1189.109734
Figure 4 Provanna morphotypes sampled from the CRMA, BP. laevis from mussel shells, Mound 12, AD4917, 965 m C, DP. ios from unknown substrate, Jaco Scar, SD214, 1803 m E Specimens of P. pacifica from sunken wood, Mound 11, AD4988, 1017 m F Specimen of P. cf. lomana from mussel shells, Quepos Seep, AD4924, 1413 m. Both the dorsal and ventral view of each shell is shown. Scale bars: 1 mm.
Figure 1 from: Betters MJ, Cordes EE (2024) New records of Provanna (Gastropoda, Provannidae) from the Costa Rica Margin and an identification key for the genus. ZooKeys 1189: 1-32. https://doi.org/10.3897/zookeys.1189.109734
Figure 1 Map of the Costa Rica Margin A overview of the Costa Rica continental shelf with hydrocarbon seep sites labelled B close-up view of the sites Mound 12 and Mound 11, which appear overlapping in the larger map. Bottom bathymetry is demarcated by black lines every 250 m.
Figure 2 from: Betters MJ, Cordes EE (2024) New records of Provanna (Gastropoda, Provannidae) from the Costa Rica Margin and an identification key for the genus. ZooKeys 1189: 1-32. https://doi.org/10.3897/zookeys.1189.109734
Figure 2 Visual definitions of morphological characters and measurements used in the study A shell morphological characters B informative measurements assessed for our own specimens C radular terminology and morphological characters. Abbreviations: SW: Shell Width, SL: Truncated Shell Length, GL: Maximum Granule Length, AL: Aperture Length, AW: Aperture Width.
Figure 8 from: Betters MJ, Cordes EE (2024) New records of Provanna (Gastropoda, Provannidae) from the Costa Rica Margin and an identification key for the genus. ZooKeys 1189: 1-32. https://doi.org/10.3897/zookeys.1189.109734
Figure 8 Bayesian phylogenetic tree of Provanna based on a 452 bp region of the mitochondrial CO1 gene. Novel sequences are bolded and highlighted in yellow. Topology was inferred using the HKY+G+I substitution model. Numbers above branch nodes represent Bayesian posterior probabilities. Numbers below branch nodes represent the proportion of replicate trees in which the associated taxa clustered together in the bootstrap test (10,000 replicates). Only values above 50 are shown. The tree is drawn to scale, with branch lengths representing the number of base substitutions accumulated over time.
Figure 6 from: Betters MJ, Cordes EE (2024) New records of Provanna (Gastropoda, Provannidae) from the Costa Rica Margin and an identification key for the genus. ZooKeys 1189: 1-32. https://doi.org/10.3897/zookeys.1189.109734
Figure 6 A the four morphotypes sampled B–F comparison of morphological traits among each morphotype. The number of individuals represented on the graph and included in one-way ANOVAs are denoted by "n =" above or below each bar. Resultant p-values from one-way ANOVAs are denoted above each graph (p-value: 0 < *** < 0.001 < ** < 0.01 < * 0.05). Provanna cf. lomana was excluded from all ANOVAs due to the small number of individuals, but is included here for graphical comparison. Note that the graphs of Shell Roundness E and Aperture Roundness F have y-axes that do not start at zero. Scale bars: 1 mm.
Figure 3 from: Betters MJ, Cordes EE (2024) New records of Provanna (Gastropoda, Provannidae) from the Costa Rica Margin and an identification key for the genus. ZooKeys 1189: 1-32. https://doi.org/10.3897/zookeys.1189.109734
Figure 3 . Examples of Provanna shell morphological variety AP. kuroshimensis, no sculpturing, growth lines present, flattened suture B–F constricted suture: BP. cooki, spiral sculpture only, no sculptural elements CP. chevalieri, axial sculpture only, no sculptural elements D–F both axial and spiral sculpturing: DP. fenestrata, sculptures about equal in strength, no sculptural elements EP. clathrata, axial sculpture stronger than spiral, blunt, sloping nodules FP. reticulata, spiral sculpture stronger than axial, minor spines.
Fig 8 from: Gudin FM, Campos LD, Redü DR, de Mello FAG (2024) Parasitoid flies (Diptera, Tachinidae) in true crickets (Orthoptera, Grylloidea): New host records from Brazil, identification key to parasitoids, and revision of host-parasitoid interactions. Journal of Orthoptera Research 33(1): 41-58. https://doi.org/10.3897/jor.33.108456
Fig 8 Exoristoides johnsoni Coquillett, 1897 (Polideini), and Anisia gilvipes (Coquillett, 1897) (Blondeliini), deposited in CNC. A, B.Exoristoides johnsoni male, lateral and dorsal habitus, respectively; C, D.Exoristoides johnsoni female, lateral and dorsal habitus, respectively, with detail (c) of metathoracic spiracle; E, F.Anisia gilvipes male, lateral and dorsal habitus, respectively; G, H.Anisia gilvipes female, lateral and dorsal habitus, respectively. Images originally lacking scales.
Fig 7 from: Gudin FM, Campos LD, Redü DR, de Mello FAG (2024) Parasitoid flies (Diptera, Tachinidae) in true crickets (Orthoptera, Grylloidea): New host records from Brazil, identification key to parasitoids, and revision of host-parasitoid interactions. Journal of Orthoptera Research 33(1): 41-58. https://doi.org/10.3897/jor.33.108456
Fig 7 Calodexia cf. venteris Curran, 1934a, reared from Guabamima lordelloi de Mello, 1993 (Phalangopsidae). A–C.Calodexia cf. venteris male, dorsal habitus, lateral habitus, and head in frontal view, respectively; D, E.Guabamima lordelloi holotype male, dorsal and lateral habitus, respectively; F, G.Guabamima lordelloi female, dorsal and lateral habitus, respectively. Scale bars: 2 mm (A–C); 5 mm (D–G).
Fig 6 from: Gudin FM, Campos LD, Redü DR, de Mello FAG (2024) Parasitoid flies (Diptera, Tachinidae) in true crickets (Orthoptera, Grylloidea): New host records from Brazil, identification key to parasitoids, and revision of host-parasitoid interactions. Journal of Orthoptera Research 33(1): 41-58. https://doi.org/10.3897/jor.33.108456
Fig 6 Calodexia cf. insolita Curran, 1934b (Tachinidae), and Stylogaster Macquart, 1835 (Conopidae), reared from Pizacris Souza-Dias and Desutter-Grandcolas, 2015 (Phalangopsidae). A–C.Calodexia cf. insolita female, dorsal habitus, lateral habitus, and head in frontal view, respectively; D.Stylogaster female, lateral habitus; E, F.Pizacris male, dorsal and lateral habitus, respectively; G.Pizacris female, lateral habitus. Scale bars: 2 mm (A–D); 5 mm (E–G).
Fig 3 from: Gudin FM, Campos LD, Redü DR, de Mello FAG (2024) Parasitoid flies (Diptera, Tachinidae) in true crickets (Orthoptera, Grylloidea): New host records from Brazil, identification key to parasitoids, and revision of host-parasitoid interactions. Journal of Orthoptera Research 33(1): 41-58. https://doi.org/10.3897/jor.33.108456
Fig 3 Calodexia cf. fasciata Curran, 1934a, reared from Eidmanacris Chopard, 1956 (Phalangopsidae). A–C.Calodexia cf. fasciata female, dorsal habitus, lateral habitus, and head in frontal view, respectively; D, E.Eidmanacris male, dorsal and lateral habitus, respectively; F, G.Eidmanacris female, dorsal and lateral habitus, respectively. Scale bars: 2 mm (A–C); 5 mm (D–G).
Fig 4 from: Gudin FM, Campos LD, Redü DR, de Mello FAG (2024) Parasitoid flies (Diptera, Tachinidae) in true crickets (Orthoptera, Grylloidea): New host records from Brazil, identification key to parasitoids, and revision of host-parasitoid interactions. Journal of Orthoptera Research 33(1): 41-58. https://doi.org/10.3897/jor.33.108456
Fig 4 Calodexia cf. flavipes (Schiner, 1868) reared from Aracamby de Mello, 1992 (Phalangopsidae). A–C.Calodexia cf. flavipes male, dorsal habitus, lateral habitus, and head in frontal view, respectively; D, E.Aracamby male, dorsal and lateral habitus, respectively; F, G.Aracamby female, dorsal and lateral habitus, respectively. Scale bars: 2 mm (A–C); 5 mm (D–G).
Fig 2 from: Gudin FM, Campos LD, Redü DR, de Mello FAG (2024) Parasitoid flies (Diptera, Tachinidae) in true crickets (Orthoptera, Grylloidea): New host records from Brazil, identification key to parasitoids, and revision of host-parasitoid interactions. Journal of Orthoptera Research 33(1): 41-58. https://doi.org/10.3897/jor.33.108456
Fig 2 Calodexia Wulp, 1891, and Ormia ochracea (Bigot, 1889), reared from Anurogryllus (Urogryllus) toledopizai (de Mello, 1988) (Gryllidae). A–C.Calodexia male, lateral habitus, dorsal habitus, and head in frontal view, respectively; D–F.Ormia ochracea male, lateral habitus, dorsal habitus, and head in frontal view, respectively, with white arrow showing callosity on costal vein; G–I.Ormia ochracea female, lateral habitus, dorsal habitus, and head in frontal view, respectively, with white arrow showing the position of the inflated basisternum and tympanal membrane; J, K.Anurogryllus (U.) toledopizai male, dorsal and lateral habitus, respectively; L, M.Anurogryllus (U.) toledopizai female, dorsal and lateral habitus, respectively. Scale bars: 2 mm (A–I); 5 mm (J–M).
Fig 5 from: Gudin FM, Campos LD, Redü DR, de Mello FAG (2024) Parasitoid flies (Diptera, Tachinidae) in true crickets (Orthoptera, Grylloidea): New host records from Brazil, identification key to parasitoids, and revision of host-parasitoid interactions. Journal of Orthoptera Research 33(1): 41-58. https://doi.org/10.3897/jor.33.108456
Fig 5 Calodexia cf. flavipes (Schiner, 1868) reared from an unidentified Phalangopsidae. A–C.Calodexia cf. flavipes male, dorsal habitus, lateral habitus, and head in frontal view, respectively. Scale bars: 2 mm (A–C); 5 mm (D–G).
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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.