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80 results for “Fly parasitoids”
Figure 3 in Novel trophic interaction: the scuttle fly Megaselia scalaris (Diptera: Phoridae) is a facultative parasitoid of the desert scorpion Mesobuthus eupeus mongolicus (Scorpiones: Buthidae)
Figure 3. Genetic divergences among the haplotypes of Megaselia scalaris are shown as NeighborNet based on p-distances of mtCOI sequences. Circle sizes are proportional to the number of isolates sharing the haplotypes. Isolates from the scorpion Mesobuthus eupeus mongolicus are all included in Hap8.
Figure 1 in Novel trophic interaction: the scuttle fly Megaselia scalaris (Diptera: Phoridae) is a facultative parasitoid of the desert scorpion Mesobuthus eupeus mongolicus (Scorpiones: Buthidae)
Figure 1. Scorpion, Mesobuthus eupeus mongolicus (a) and its parasitoid scuttle fly, Megaselia scalaris (b–e): (a) a female scorpion; (b) larvae of fly emerging from the genital operculum of scorpion; (c) fly larva; (d) fly pupa; (e) a male fly.
FIGURES 1–3. Female phorid fly oviscapes, lateral. 1 in Parasitoid phorid flies (Diptera: Phoridae) from the threatened leafcutter ant Atta robusta Borgmeier (Hymenoptera: Formicidae)
FIGURES 1–3. Female phorid fly oviscapes, lateral. 1. Eibesfeldtphora breviloba; 2. Eibesfeldtphora digitalis; 3. Myrmosicarius exrobustus.
Data from: Selection on fruit traits is mediated by the interplay between frugivorous birds, fruit flies, parasitoid wasps, and seed-dispersing ants
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Data from: Molecular biogeography and host relations of a parasitoid fly
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Figure 1 from: Cruz-Bustos J, Montoya P, Pérez-Lachaud G, Valle-Mora J, Liedo P (2020) Biological attributes of diapausing and non-diapausing Doryctobracon areolatus (Hymenoptera, Braconidae), a parasitoid of Anastrepha spp. (Diptera, Tephritidae) fruit flies. Journal of Hymenoptera Research 78: 41-56. https://doi.org/10.3897/jhr.78.52269
Figure 1 Duration of development of non-diapausing and diapausing Doryctobracon areolatus females and males, parasitizing Anastrepha ludens larvae.
Figure 5 from: Cruz-Bustos J, Montoya P, Pérez-Lachaud G, Valle-Mora J, Liedo P (2020) Biological attributes of diapausing and non-diapausing Doryctobracon areolatus (Hymenoptera, Braconidae), a parasitoid of Anastrepha spp. (Diptera, Tephritidae) fruit flies. Journal of Hymenoptera Research 78: 41-56. https://doi.org/10.3897/jhr.78.52269
Figure 5 Net fecundity of Doryctobracon areolatus females from A non-diapausing and B diapausing cohorts.
Figure 3 from: Cruz-Bustos J, Montoya P, Pérez-Lachaud G, Valle-Mora J, Liedo P (2020) Biological attributes of diapausing and non-diapausing Doryctobracon areolatus (Hymenoptera, Braconidae), a parasitoid of Anastrepha spp. (Diptera, Tephritidae) fruit flies. Journal of Hymenoptera Research 78: 41-56. https://doi.org/10.3897/jhr.78.52269
Figure 3 Canonical analysis of adult parasitoids' morphological data from non-diapausing and diapausing Doryctobracon areolatus. A Comparison by type of development B comparison among females C comparison between sexes. The asterisk (*) indicates a significant difference.
Figure 2 from: Cruz-Bustos J, Montoya P, Pérez-Lachaud G, Valle-Mora J, Liedo P (2020) Biological attributes of diapausing and non-diapausing Doryctobracon areolatus (Hymenoptera, Braconidae), a parasitoid of Anastrepha spp. (Diptera, Tephritidae) fruit flies. Journal of Hymenoptera Research 78: 41-56. https://doi.org/10.3897/jhr.78.52269
Figure 2 Canonical analysis of morphological data from puparia containing non-diapausing and diapausing male and female Doryctobracon areolatus parasitoids. The asterisk (*) indicates a significant difference.
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 4 from: Ayala A, Pérez-Lachaud G, Toledo J, Liedo P, Montoya P (2018) Host acceptance by three native braconid parasitoid species attacking larvae of the Mexican fruit fly, Anastrepha ludens (Diptera, Tephritidae). Journal of Hymenoptera Research 63: 33-49. https://doi.org/10.3897/jhr.63.23724
Figure 4 Latency (average ± SE, in minutes) between ovipositions of three native opine parasitoids attacking non-parasitized and previously parasitized Anastrepha ludens larvae. Different capital letters indicate statistically significant difference between the bars. Different letters, indicate statistically significant difference between the bars. Different lower case letters, indicate statistically significant difference between species.
Figure 2 from: Ayala A, Pérez-Lachaud G, Toledo J, Liedo P, Montoya P (2018) Host acceptance by three native braconid parasitoid species attacking larvae of the Mexican fruit fly, Anastrepha ludens (Diptera, Tephritidae). Journal of Hymenoptera Research 63: 33-49. https://doi.org/10.3897/jhr.63.23724
Figure 2 Ethogram of oviposition of females of Utetes anastrephae on non-parasitized larvae (a) and larvae previously parasitized by conspecifics (b) under laboratory conditions. The width of the arrow is proportional to the relative frequency of transition. The numbers associated with the arrows represent the observed frequencies of the successive behaviors of a complex sequence of behavior (proportions are indicated in parentheses).
Figure 3 from: Ayala A, Pérez-Lachaud G, Toledo J, Liedo P, Montoya P (2018) Host acceptance by three native braconid parasitoid species attacking larvae of the Mexican fruit fly, Anastrepha ludens (Diptera, Tephritidae). Journal of Hymenoptera Research 63: 33-49. https://doi.org/10.3897/jhr.63.23724
Figure 3 Ethogram of oviposition of females of Opius hirtus on non-parasitized larvae (a) and larvae previously parasitized by conspecifics (b) under laboratory conditions. The width of the arrow is proportional to the relative frequency of transition. The numbers associated with the arrows represent the observed frequencies of the successive behaviors of a complex sequence of behavior (proportions are indicated in parentheses).
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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.