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66 results for “interactive identification keys”
FIGURE 2 in A new group of species of the genus Megalothorax (Collembola, Neelidae) with Gondwanan distribution, and introducing an open interactive identification key of Megalothorax species
FIGURE 2. Megalothorax anterolenis sp. nov. (A, B) Labrum anterior process, (A) posterior side, (B) anterior side. (C) Maxillary outer lobe internal side. (D) Mandibula. (E) Maxilla. (F, G) Antenna (F) posterior side, (G) anterior side. (H) Abd. VI tergite and sternite, Abd. V and IV sternites, and posterior side of manubrium and dens (furca), chaeta and lobe in dotted line are missing on the figured specimen but normally present. (I) dens anterior side. (J) Mucro.
FIGURE 8 in A new group of species of the genus Megalothorax (Collembola, Neelidae) with Gondwanan distribution, and introducing an open interactive identification key of Megalothorax species
FIGURE 8. (A) Diagram of dorsal head chaetotaxy, chaeta in blue present only in M. tasmanterolenis sp. nov. and M. zealanterolenis sp. nov., channel in blue present only in M. tasmanterolenis sp. nov. (B) Diagram of ventral head chaetotaxy. (C) Diagram of antenna chaetotaxy. (D) Body chaetotaxy diagram, s-chaetae shape based on M. anterolenis sp. nov. (E) Connection of integumentary channels and linea ventralis: (a) crossed, (b) transitional form, (c) circular.
FIGURE 7 in A new group of species of the genus Megalothorax (Collembola, Neelidae) with Gondwanan distribution, and introducing an open interactive identification key of Megalothorax species
FIGURE 7. Megalothorax zealanterolenis sp. nov. (A) chaetae of Abd. IV sternites. (B) Leg I. (C) Leg II. (D) Leg III. (E) Claw I. (F) Claw II. (G) Claw III. (H, I, J) Mucro variations.
FIGURE 10 in A new group of species of the genus Megalothorax (Collembola, Neelidae) with Gondwanan distribution, and introducing an open interactive identification key of Megalothorax species
FIGURE 10. Molecular phylogeny of the genus Megalothorax, with optimization of taxonomically relevant character states. New OTUs names are indicated in bold. Bootstrap node support is shown next to the node, only when below 100 %.
Figure 2 in Development of an interactive identification key for Oncaeidae (Copepoda: Cyclopoida)
Figure 2. Leg armature types of oncaeid copepods, grouped according to the spine counts on the exo- and endopods of swimming legs P1 to P4. The number of oncaeid species per armature type is shown on the y-axis. Leg armature type 1 denotes the typical leg armature of oncaeid copepods (cf. Böttger-Schnack and Schnack 2013, table 4), armature type 2 to 14 differ in spine count on the exo- and/or endopods from type 1 (cf. Böttger-Schnack and Schnack 2013, tables 5 and 6). Question marks denote the estimated number of additional, yet undescribed species of that armature type.
Figure 1 in Development of an interactive identification key for Oncaeidae (Copepoda: Cyclopoida)
Figure 1. Screen shot of the Lucid identification key for Oncaeidae, with morphological characters ('features') presented in the top left window, and the copepod taxa (called 'entities') in the top right window. Features and entities (taxa) are organized in several levels of subgrouping and presented as trees, which are partly expanded.
Figure 8 in Development of an interactive identification key for Oncaeidae (Copepoda: Cyclopoida)
Figure 8. Characteristics of P4 endopod (enlarged) in oncaeid species. (A) Conical process present between the two distal spines of P4 endopod (Triconia minuta [from Böttger- Schnack 1999]); (B) Conical process absent (Oncaea paraclevei [from Böttger- Schnack 2001]).
Figure 3 in Development of an interactive identification key for Oncaeidae (Copepoda: Cyclopoida)
Figure 3. Body length of oncaeid copepod species: illustration of size difference between largesized species (Oncaea venusta f. typica [from Böttger-Schnack 2001]) and small-sized species (O. atlantica [from Boxshall and Böttger 1987]).
Figure 7 in Development of an interactive identification key for Oncaeidae (Copepoda: Cyclopoida)
Figure 7. Form types of maxilliped basis (shaded) in oncaeid species: compact (Oncaea compacta [from Heron 1977]); robust-oblong (O. venusta f. typica [from Böttger-Schnack 2001]); elongate (O. bispinosa [from Böttger-Schnack 2002]); very long and narrow (O. tenuimana [original]).
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).
Fig 1 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 1 Anisia Wulp, 1890, reared from Aracamby de Mello, 1992 (Phalangopsidae). A–C.Anisia female, 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).
Figure 9 from: Rousse P, Broad G, van Noort S (2016) Review of the genus Genaemirum Heinrich (Ichneumonidae, Ichneumoninae) with interactive identification keys to species. ZooKeys 635: 77-105. https://doi.org/10.3897/zookeys.636.10216
Figure 9 - Genaemirum varianum (Tosquinet). Holotype male. A habitus lateral view (inset: data labels) B head, mesosoma, dorsal view C head anterior view D head, mesosoma anterior-lateral view E metasomal tergites 1-4 dorsal view F propodeum, dorsal view.
Figure 10 from: Rousse P, Broad G, van Noort S (2016) Review of the genus Genaemirum Heinrich (Ichneumonidae, Ichneumoninae) with interactive identification keys to species. ZooKeys 635: 77-105. https://doi.org/10.3897/zookeys.636.10216
Figure 10 - Genaemirum vulcanicola Heinrich. Holotype female. A habitus lateral view (inset: data labels) B head, mesosoma, dorsal view C head anterior view D head, mesosoma anterior-lateral view E metasomal tergites 1-4 dorsal view F propodeum, dorsal view.
Figure 7 from: Rousse P, Broad G, van Noort S (2016) Review of the genus Genaemirum Heinrich (Ichneumonidae, Ichneumoninae) with interactive identification keys to species. ZooKeys 635: 77-105. https://doi.org/10.3897/zookeys.636.10216
Figure 7 - Genaemirum rhinoceros Heinrich. Holotype female. A habitus lateral view (inset: data labels) B head, mesosoma, dorsal view C head anterior view D head, pronotum anterior-lateral view E metasomal tergites 1-2 dorsal view F propodeum, dorsal view.
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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.