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Fig. 4 in Taxonomic revision of Australian Amobia Robineau-Desvoidy, 1830 (Sarcophagidae: Miltogramminae): integrating morphology and genetics finds a new species and tackles old problems
Fig. 4. Amobia burnsi (Malloch, 1930), ♂, NSW, North Head, Sydney Harbour, 14 Feb. 1978, G. Daniels leg. (AM) A. Habitus, lateral view. B. Head, lateral view. C. Habitus, dorsal view. D. Head, dorsal view. E. Abdomen, dorsal view. F. Left wing, dorsal view. G. Head, anterior view. Scale bars: 1 mm.
Fig. 1 in Taxonomic revision of Australian Amobia Robineau-Desvoidy, 1830 (Sarcophagidae: Miltogramminae): integrating morphology and genetics finds a new species and tackles old problems
Fig. 1. Maximum likelihood phylogenetic tree indicating the placement of Amobia among the global Miltogramminae, inferred from COI, CYTB, ND4 and EF1α sequence data. With the exception of the three newly sequenced Australian Amobia and Macronychia rubesca, data was acquired from Piwczyński et al. (2017). Node support values are shown for both maximum likelihood analysis (bootstrap support, 1000 iterations; in bold font) and Bayesian analysis (posterior probability, 40 million generations), 'NA' indicates nodes resolved that were not resolved by the Bayesian analysis. Branch length scale = 0.3 nucleotide substitutions per site (calculated by the GTR+G nucleotide substitution model).
Fig. 6 in Taxonomic revision of Australian Amobia Robineau-Desvoidy, 1830 (Sarcophagidae: Miltogramminae): integrating morphology and genetics finds a new species and tackles old problems
Fig. 6. Amobia serpenta sp. nov., holotype, ♂, NT, Serpentine Gorge, West MacDonnell National Park, 13 Nov. 2017, Johnston, Wallman and Szpila leg. (ANIC). A. Habitus, lateral view. B. Head, lateral view. C. Habitus, dorsal view. D. Head, dorsal view. E. Abdomen, dorsal view. F. Left wing, dorsal view. G. Head, anterior view. Scale bars: 1 mm.
Fig. 3 in Taxonomic revision of Australian Amobia Robineau-Desvoidy, 1830 (Sarcophagidae: Miltogramminae): integrating morphology and genetics finds a new species and tackles old problems
Fig. 3. Amobia auriceps (Baranov, 1935), male terminalia, QLD, Cairns, 1919, J.F. Illingworth leg. (BM). A. Epandrium, cerci, surstyli and phallus, posterior view. B. Epandrium, cerci, surstyli, phallus and pre-gonite, lateral view. Abbreviations: c = cercus; d = distal lobe of phallus; s = surstylus; p = pregonite. Scale bars: 100 µm.
Fig. 5 in Taxonomic revision of Australian Amobia Robineau-Desvoidy, 1830 (Sarcophagidae: Miltogramminae): integrating morphology and genetics finds a new species and tackles old problems
Fig. 5. Amobia burnsi (Malloch, 1930), male terminalia, NT, 15 km N Katherine, 16 May 2005, R.W. Matthews leg (ANIC). A. Epandrium, cerci, surstyli and phallus, posterior view. B. Epandrium, cerci, surstyli, phallus and pre-gonite, lateral view. C. SEM image of epandrium, gonites, cerci and surstyli, posterior view. D. SEM image of epandrium, gonites, phallus, cerci and surstyli, lateral view. Abbreviations: c = cercus; d = distal lobe of phallus; s = surstylus; p = pre-gonite. Scale bars: 100 µm.
Figures 1–3. Pepsis spp., female habitus. 1 in The Pepsis menechma Lepeletier (Hymenoptera: Pompilidae: Pepsinae) taxonomic and nomenclatural problem
Figures 1–3. Pepsis spp., female habitus. 1) Pepsis elegans female habitus, Atlanta, Fulton County, Georgia. Photograph © Brenna Decker. 2) Pepsis cerberus female habitus, Florida Canyon, Pima County, Arizona. Photograph © Chris Grinter. 3) Pepsis novitia female habitus, Tampico, Tamaulipas State, Mexico. Photograph © Brittany Kohler.
Figure 10. Geographic location map for Pepsis cerberus, P in The Pepsis menechma Lepeletier (Hymenoptera: Pompilidae: Pepsinae) taxonomic and nomenclatural problem
Figure 10. Geographic location map for Pepsis cerberus, P. elegans, and P. novitia in the Nearctic Region (based on Brimley 1936; Hurd 1952; Krombein 1952; Johnston 2000; Bond and Opell 2002; Vardy 2005; Leavengood et al. 2011; Bond and Godwin 2013; Hamilton et al. 2016; Norden 2017; Godwin and Bond 2021; Durand, pers. comm.; BugGuide.net; flickr.com; iNaturalist.org; gbif.org; SCAN; and specimen records from 36 insect collections as listed in Materials and Methods). Black lines represent range limits of potential host spider genera. Solid black line represents geographic limit of Ummidia (Halonoproctidae) species (Godwin and Bond 2021). Dashed black line represents geographic limit of Aphonopelma (Theraphosidae) species (Hamilton et al. 2016). Dotted black line represents geographic limit of Eucteniza (Euctenizidae) species (Bond and Godwin 2013). Dash-dotted black line represents geographic limit of Entychides Simon (Euctenizidae) species (Bond and Opell 2002).
Figures 7–9. Pepsis spp., female antennae. 7 in The Pepsis menechma Lepeletier (Hymenoptera: Pompilidae: Pepsinae) taxonomic and nomenclatural problem
Figures 7–9. Pepsis spp., female antennae. 7) Pepsis elegans female antennae with short, wide, yellowish orange flagellomeres, Biloxi, Harrison County, Mississippi. Photograph © Brenna Decker. 8) Pepsis cerberus female antennae with longer, narrower, black flagellomeres, Box Canyon, Pima County, Arizona. Photograph © Brenna Decker. 9) Pepsis novitia female antennae with intermediate length, orange apical and brown proximal flagellomeres, Tampico, Tamaulipas State, Mexico. Photograph © Brittany Kohler.
Figures 4–6 in The Pepsis menechma Lepeletier (Hymenoptera: Pompilidae: Pepsinae) taxonomic and nomenclatural problem
Figures 4–6. Pepsis spp., female upper surface of hind tibia. 4) Pepsis cerberus female upper surface of hind tibia with moderately small conical serrations and numerous, long, stout, posterior-curved bristles, Box Canyon, Pima County, Arizona. Photograph © Brenna Decker. 5) Pepsis elegans female upper surface of hind tibia with small conical serrations and sparser, shorter, thinner, straighter bristles, Biloxi, Harrison County, Mississippi. Photograph © Brenna Decker. 6) Pepsis novitia female upper surface of hind tibia with moderately small conical serrations and numerous long, stout, posterior-curved bristles, Tampico, Tamaulipas State, Mexico. Photograph © Brittany Kohler.
Figure 2 in The problem of taxonomic uncertainty in biosecurity: South African mite interceptions as an example
Figure 2 Images of slide-mounted specimens, showing features which could clearly distinguish the intercepted unknownBrevipalpus species,
Figure 1 in The problem of taxonomic uncertainty in biosecurity: South African mite interceptions as an example
Figure 1 South African biosecurity personnel inspecting imported kiwifruit for insects and mites. Images have been edited to remove sensitive information, including identity of personnel.
Fig. 1 in DNA barcode of Parodontidae species from the La Plata river basin - applying new data to clarify taxonomic problems
Fig. 1. Map of the La Plata River basin showing the localities of Parodontidae samples used in this study. Empty pentagon: P. nasus; full pentagon: A. affinis; empty star: P. moreirai; full star: A. affinis; empty square: A. vittatus; full square: A. piracicabae; empty lozenge: Apareiodon sp.; full lozenge: A. vladii; empty triangle: A. affinis; full triangle: A. ibitiensis. The Iguaçu Falls and the Itaipu hydroelectric Power Plant are located in the city of Foz do Iguaçu, PR and the old Seven Falls in the city of Guaíra, PR - shown on the map.
Fig. 2. K2P in DNA barcode of Parodontidae species from the La Plata river basin - applying new data to clarify taxonomic problems
Fig. 2. K2P distance NJ dendrogram showing the nine analyzed species/populations of Parodontidae from the La Plata River basin.
Figs. 4-5 in First record of Zelus armillatus (Lepeletier & Serville, 1825) in Costa Rica, with notes on taxonomic problems regarding the genus Zelus Fabricius, 1803 (Hemiptera: Heteroptera: Reduviidae: Harpactorinae: Harpactorini).
Figs. 4-5.- Zelus armillatus (Lepeletier & Serville, 1825), Vuelta de Jorco, Aserrí, San José, Costa Rica, 5.8.2014. 4.- Male, lateral view. 5.- Male, dorsal view. (All photographs: Ignacio Gamboa Hidalgo.)
Fig. 6 in Guess who? Taxonomic problems in the genus Eiseniella revisited by integrated approach
Fig. 6 Predicted secondary structures of 28S gene for Spanish and Italian specimens from the studied populations and of six different species: A. trapezoides, A. dubiosa, D. octaedra, D. byblica, I. albo-
Fig. 5 in Guess who? Taxonomic problems in the genus Eiseniella revisited by integrated approach
Fig. 5 Haplotype network based on 28S. Each black circle represents a different haplotype; their size is proportional to the number of samples belonging to that haplotype. Each perpendicular line indicates a mutational step, if there were more than four it is shown with the number of mutational steps. White circles are hypothetical intermediate haplotypes. Branch length does not contain any information
Fig. 3 in Guess who? Taxonomic problems in the genus Eiseniella revisited by integrated approach
Fig. 3 Bayesian inference (BI) of the phylogenetic tree of lumbricids based on concatenated sequences of COI, 16S, 28S, 12S, and ND1 (long dataset). Posterior probability/bootstrap support values (of maximum likelihood analysis, ML) are shown as black squares when higher than 0.9/0.7 (BI/ML). Gray triangles represent two or more species of a genus-level clade collapsed to facilitate interpretation of
Fig. 1 in Guess who? Taxonomic problems in the genus Eiseniella revisited by integrated approach
Fig. 1 Localities sampled. GPS coordinates and number of specimens collected can be found in Supplementary Table 1. Specimens from Italy (3, 4, 5, 6, 7, 8, and 9) and Cyprus (2) belong to E. neapolitana. Specimens from Spain (1) belong to N. andaluciana
Fig. 4 in Guess who? Taxonomic problems in the genus Eiseniella revisited by integrated approach
Fig. 4 Haplotype network based on COI. Each black circle represents a different haplotype; their size is proportional to the number of samples belonging to that haplotype. Each perpendicular line indicates a mutational step; if there were more than four, it is shown with the number of mutational steps. White circles are hypothetical intermediate haplotypes. Branch length does not contain any information
Fig. 9 in Guess who? Taxonomic problems in the genus Eiseniella revisited by integrated approach
Fig. 9 Box-plot diagram of number of segments in the studied populations and E. tetraedra. Different letters indicate different groups in multiple range tests
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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.