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911 results for “new host records”
FIGURES 47–48. Mesoventrite, postmesocoxal sulcus Merobruchus. 47. M in A key to American genus Merobruchus Bridwell (Coleoptera: Chrysomelidae: Bruchinae) with descriptions of species and two new host plant records for the subfamily
FIGURES 47–48. Mesoventrite, postmesocoxal sulcus Merobruchus. 47. M. major; 48. M. paquetae.
FIGURE 1 in A new species of Acanthocaudus Smith (Braconidae: Aphidiinae), with a key to species and new host and distribution records for aphidiines associated with Silphium perfoliatum L. (Asterales: Asteraceae)
FIGURE 1. Lateral habitus, Acanthocaudus bicolor Kula, new species, based on type series.
FIGURE 43 in Redescription of the numbat tick Ixodes (Sternalixodes) myrmecobii Roberts, 1962 (Acari: Ixodidae) with descriptions of the male and nymph, and new host records
FIGURE 43. Distribution of Ixodes myrmecobii in Australia based on museum and published records.
Fig. 2 in New Distribution and Host Records for the GenusZabrotesHorn (Coleoptera: Bruchidae)
Fig. 2. Rhynchosia seed showing Zabrotes sinaloensis emerging.
Fig. 1 in New Distribution and Host Records for the GenusZabrotesHorn (Coleoptera: Bruchidae)
Fig. 1. Dorsal (left) and lateral (right) views of an adult male of Zabrotes sinaloensis.
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 2 from: Chen X-M, Tang X, Ma J, Liu N-G, Tibpromma S, Karunarathna SC, Xiao Y-P, Lu Y-Z (2024) Identification of two new species and a new host record of Distoseptispora (Distoseptisporaceae, Distoseptisporales, Sordariomycetes) from terrestrial and freshwater habitats in Southern China. MycoKeys 102: 83-105. https://doi.org/10.3897/mycokeys.102.115452
Figure 2 Distoseptispora hainanensis (GZAAS 22-2047, holotype) a, b colonies on substrate c–e conidiophores and conidia f–h conidiogenous cells bearing conidia i, j conidiophores k–q conidia r, s colony on PDA (r from front s from reverse). Scale bars: 50 μm (c, d, f–j, l–q); 30 μm (e, k).
Figure 1 from: Chen X-M, Tang X, Ma J, Liu N-G, Tibpromma S, Karunarathna SC, Xiao Y-P, Lu Y-Z (2024) Identification of two new species and a new host record of Distoseptispora (Distoseptisporaceae, Distoseptisporales, Sordariomycetes) from terrestrial and freshwater habitats in Southern China. MycoKeys 102: 83-105. https://doi.org/10.3897/mycokeys.102.115452
Figure 1 Phylogenetic tree generated from ML analysis based on a combination of LSU, ITS, tef1-a, and rpb2 sequence data. Bootstrap support values of ML and MP equal to or greater than 75%, and PP value equal to or greater than 0.95 are given near the nodes as ML/PP/MP. The tree is rooted with Aquapteridospora aquatica (MFLUCC 17-2371). Ex-type strains are indicated by the superscript T. The new collections are in bold red text.
Figure 4 from: Chen X-M, Tang X, Ma J, Liu N-G, Tibpromma S, Karunarathna SC, Xiao Y-P, Lu Y-Z (2024) Identification of two new species and a new host record of Distoseptispora (Distoseptisporaceae, Distoseptisporales, Sordariomycetes) from terrestrial and freshwater habitats in Southern China. MycoKeys 102: 83-105. https://doi.org/10.3897/mycokeys.102.115452
Figure 4 Distoseptispora tectonae (GZAAS 22-2046) a, b colonies on substrate c, d conidiophores and conidia e, f conidiophores g–k conidia l germinated conidium m, n colonies on PDA (m from front n from reverse) Scale bars: 50 μm (c, d, g–l); 20 μm (e, f).
Figure 3 from: Chen X-M, Tang X, Ma J, Liu N-G, Tibpromma S, Karunarathna SC, Xiao Y-P, Lu Y-Z (2024) Identification of two new species and a new host record of Distoseptispora (Distoseptisporaceae, Distoseptisporales, Sordariomycetes) from terrestrial and freshwater habitats in Southern China. MycoKeys 102: 83-105. https://doi.org/10.3897/mycokeys.102.115452
Figure 3 Distoseptispora lanceolatispora (GZAAS 22-2045, holotype) a, b colonies on substrate c–e conidiophores and conidia f, g conidiogenous cells bearing conidia h–k conidia l germinated conidium m, n colony on PDA (m from front n from reverse). Scale bars: 50 μm (c–g); 30 μm (h–l).
Figure 8 from: Ota Y, Erasmus A, Grutter AS, Smit NJ (2024) Two new species and new host and distribution records of Gnathia Leach, 1814 (Crustacea, Isopoda, Gnathiidae) from Western Australia and the Great Barrier Reef, Australia. ZooKeys 1193: 125-144. https://doi.org/10.3897/zookeys.1193.116538
Figure 8 Scanning electron micrograph of the ventral view of the frontal border of Gnathia aff. maculosa Ota & Hirose, 2009 (QM W29821) showing bundles of several long setae (two arrows). Scale bar: 500 µm.
Figure 7 from: Ota Y, Erasmus A, Grutter AS, Smit NJ (2024) Two new species and new host and distribution records of Gnathia Leach, 1814 (Crustacea, Isopoda, Gnathiidae) from Western Australia and the Great Barrier Reef, Australia. ZooKeys 1193: 125-144. https://doi.org/10.3897/zookeys.1193.116538
Figure 7 Gnathia aff. maculosa Ota and Hirose, 2009 (A–D; QM W29822) and G. trimaculata Coetzee, Smit, Grutter & Davies, 2009 (E; QM W29825) A whole body (dorsal view) B pereonite 1, cephalosome, and mandible (dorsal view) C pleotelson (dorsal view) D right pylopod (ventral view) E frontal border of G. trimaculata (dorsal view).
Figure 6 from: Ota Y, Erasmus A, Grutter AS, Smit NJ (2024) Two new species and new host and distribution records of Gnathia Leach, 1814 (Crustacea, Isopoda, Gnathiidae) from Western Australia and the Great Barrier Reef, Australia. ZooKeys 1193: 125-144. https://doi.org/10.3897/zookeys.1193.116538
Figure 6 Gnathia taurus sp. nov. (holotype QM W29819) A right maxilliped (ventral view) B right pylopod (ventral view) C right pereopod 2 (lateral view) D penes (ventral view) E. right pleopod 2.
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)
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.