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24 results for “phoresy”
Figure 2 in First record of phoresy on the genus Oreodera Audinet-Serville, 1835 (Coleoptera: Cerambycidae) by the pseudoscorpion Cordylochernes scorpioides (Linnaeus, 1758) (Arachnida: Pseudoscorpiones)
Figure 2. Illustration of the male Cordylochernes scorpioides (Linnaeus, 1758) (Chernetidae) hidden under the elytra of Oreodera rufofasciata Bates, 1861. Scale bar: 1 cm. / Ilustración del macho Cordylochernes scorpioides (Linnaeus, 1758) (Chernetidae) escondido bajo los élitros de Oreodera
Figure 1. A-B in Phoresy of Americhernes oblongus (Say) (Pseudoscorpiones: Chernetidae) in a species of the genus Scipopus Enderlein (Diptera: Micropezidae)
Figure 1. A-B. Pseudoscorpion Americhernes oblongus on the coxa of the hind leg of Scipopus sp. C. Ventral habitus of A. oblongus. Scale= 0.5 mm
Fig. 5 in Ectoparasites of hedgehogs: From flea mite phoresy to their role as vectors of pathogens
Fig. 5. Phylogenetic analysis of the 16S rRNA gene (281 bp) of Ehrlichia and Anaplasma spp. detected in this study (Bold) and relationship with other Ehrlichia/ Anaplasma spp. The evolutionary history was inferred by using the Maximum Likelihood method based on the Kimura 2-parameter model (Kimura, 1980). Initial tree (s) for the heuristic search were obtained automatically by applying Neighbor-Join and BioNJ algorithms to a matrix of pairwise distances estimated using the Maximum Composite Likelihood (MCL) approach, and then selecting the topology with superior log likelihood value. The rate variation model allowed for some sites to be evolutionarily invariable ([+I], 37.72% sites). GenBank accession number and country of origin are presented for each sequence.
Fig. 3 in Ectoparasites of hedgehogs: From flea mite phoresy to their role as vectors of pathogens
Fig. 3. Phylogenetic analysis of the gltA gene (345 bp) of Rickettsia asembonensis detected in this study (Bold) and relationship with other Rickettsia spp. The evolutionary history was inferred by using the Maximum Likelihood method based on the Tamura 3-parameter model (Tamura, 1992). A discrete Gamma distribution was used to model evolutionary rate differences among sites (5 categories [+G, parameter = 0.2157]). GenBank accession number and country of origin are presented for each sequence.
Fig. 4 in Ectoparasites of hedgehogs: From flea mite phoresy to their role as vectors of pathogens
Fig. 4. Phylogenetic analysis of the ompA gene (579 bp) of Rickettsia slovaca and Rickettsia massiliae detected in this study (Bold) and relationship with other Rickettsia spp. The evolutionary history was inferred by using the Maximum Likelihood method based on the Tamura 3-parameter model (Tamura, 1992). Initial tree(s) for the heuristic search were obtained automatically by applying Neighbor-Join and BioNJ algorithms to a matrix of pairwise distances estimated using the Maximum Composite Likelihood (MCL) approach, and then selecting the topology with superior log likelihood value. The rate variation model allowed for some sites to be evolutionarily invariable ([+I], 20.90% sites). GenBank accession number and country of origin are presented for each sequence.
Fig. 1 in Phoresy of a sucking louse, Linognathus sp. (Phthiraptera: Anoplura: Linognathidae), by Musca (Byomya) conducens Walker (Diptera: Muscidae) in South Africa
Fig. 1. Photograph of the phoretic Linognathus sp. (Anoplura, Linognathidae) attached to the right mid tarsus of Musca conducens Walker (Muscidae).
Figure 1 in A case of phoresis of midges on Zygoptera
Figure 1. Cases of Rheotanytarsus sp. on Calopteryx virgo meridionalis larvae. Photo: Ricard Martin.
Fig. 1 in Ectoparasites of hedgehogs: From flea mite phoresy to their role as vectors of pathogens
Fig. 1. Map of the study area where hedgehogs were captured. A. Italy; B. Iran.
Fig. 2 in Ectoparasites of hedgehogs: From flea mite phoresy to their role as vectors of pathogens
Fig. 2. Caparinia tripilis mites in phoretic association with Archaeopsylla erinacei flea.
Fig. 1 in Implications of a Dating Analysis of Hippoboscoidea (Diptera) for the Origins of Phoresis in Feather Lice (Psocodea: Phthiraptera: Philopteridae)
Fig. 1. Result of the MCMCTree dating analysis of the published Hippoboscoidea NCBI popset of four genes (CO1, CAD, 16s, 28s; Petersen et al. 2007). Bootstrap support is depicted to the left of nodes.The scale bar depicts divergence estimates in millions of years (Mya) and 95% highest probability distribution (HPD) are to the right of nodes. Red branches represent avian-feeding Hippoboscidae lineages. Feather louse images above scientific names indicate the genus or species below has records of louse phoresis (Ornithoctona has records of louse phoresis for three species, but the specimen analyzed was not identified to species level; a single record of louse phoresis exists for Crataerina, but is believed to be inaccurate because members of the genus are stenopterous; Corbet 1956, Keirans 1975). Illustrations of animals to the right of scientific names show host associations of Hippoboscoidea species with true ectoparasitism (Maa 1969).
Figure 3 in Ectoparasitism and phoresy in Thysanoptera: the case of Aulacothrips dictyotus (Heterothripidae) in the Neotropical savanna
Figure 3. (A) Arrows indicate two adult thrips (Aulacothrips dictyotus) next to an adult membracid (Enchenopa brasiliensis) tended by a Camponotus sp.1 ant on a leaf of Solanum lycocarpum in the Neotropical savanna; (B) the arrow indicates the red larva of A. dictyotus fixed on the ventral part of a membracid nymph body; (C) a host-free thrip larva approaching from the side of an adult membracid; (D) the arrows indicate the convoluted and continuous sensoria on adult thrip antennae.
Figure 2 in Ectoparasitism and phoresy in Thysanoptera: the case of Aulacothrips dictyotus (Heterothripidae) in the Neotropical savanna
Figure 2. The number of Enchenopa brasiliensis adults and nymphs supporting Aulacothrips dictyotus. Infestation by thrips was higher in membracid nymphs, as indicated by ∗ upon the bar.
Figure 1 in Ectoparasitism and phoresy in Thysanoptera: the case of Aulacothrips dictyotus (Heterothripidae) in the Neotropical savanna
Figure 1. The number (¯X ± 1SD) of adult and immature (A) Enchenopa brasiliensis and (B) Aulacothrips dictyotus found on Solanum lycocarpum. (∗ upon the bars indicates statistically significant differences).
FIGURES 16–19. Antennoseius perseus n in Phase morphs and phoresy: New species of Antennoseius (Vitzthumia) mites (Acari: Mesostigmata: Ascidae) associated with pyrophilous carabids (Carabidae: Sericoda spp.) in Alberta, Canada
FIGURES 16–19. Antennoseius perseus n. sp., male. 16, Dorsal shield; 17, Ventral shields; 18, Tectum; 19, Right chelicera, lateral view.
FIGURES 24–28. Antennoseius pyrophilus n in Phase morphs and phoresy: New species of Antennoseius (Vitzthumia) mites (Acari: Mesostigmata: Ascidae) associated with pyrophilous carabids (Carabidae: Sericoda spp.) in Alberta, Canada
FIGURES 24–28. Antennoseius pyrophilus n. sp., female, phoretic form. 24, Subcapitulum; 25, Right chelicera, lateral view; 26, Left palp (tarsus not shown except palp apotele), dorsal view; 27, Right leg I (except tarsus), postero-dorsal view; 28, Right leg III, postero-dorsal view.
FIGURES 20–23. Antennoseius pyrophilus n in Phase morphs and phoresy: New species of Antennoseius (Vitzthumia) mites (Acari: Mesostigmata: Ascidae) associated with pyrophilous carabids (Carabidae: Sericoda spp.) in Alberta, Canada
FIGURES 20–23. Antennoseius pyrophilus n. sp., female, phoretic form. 20, Dorsal shields; 21, Tritosternum; 22, Ventral shields; 23, Tectum and its variants.
FIGURES 14–15. Antennoseius perseus n in Phase morphs and phoresy: New species of Antennoseius (Vitzthumia) mites (Acari: Mesostigmata: Ascidae) associated with pyrophilous carabids (Carabidae: Sericoda spp.) in Alberta, Canada
FIGURES 14–15. Antennoseius perseus n. sp., female, free-living form. 14, Right leg I (except tarsus), postero-dorsal view; 15, Right leg III, postero-dorsal view.
FIGURES 5–9. Antennoseius perseus n in Phase morphs and phoresy: New species of Antennoseius (Vitzthumia) mites (Acari: Mesostigmata: Ascidae) associated with pyrophilous carabids (Carabidae: Sericoda spp.) in Alberta, Canada
FIGURES 5–9. Antennoseius perseus n. sp., female, phoretic form. 5, Subcapitulum; 6, Scanning electron micrograph of palpcoxal seta; 7, Right chelicera, lateral (antiaxial) view; 8, Right leg I (except tarsus), postero-lateral view; 9, Right leg III, dorsal view.
FIGURES 1–4. Antennoseius perseus n in Phase morphs and phoresy: New species of Antennoseius (Vitzthumia) mites (Acari: Mesostigmata: Ascidae) associated with pyrophilous carabids (Carabidae: Sericoda spp.) in Alberta, Canada
FIGURES 1–4. Antennoseius perseus n. sp., female, phoretic form. 1, Dorsal shields; 2, Scanning electron micrograph of anterior portion of podonotal shield and most of leg I; 3, Ventral shields; 4, Tectum.
FIGURES 10–13. Antennoseius perseus n in Phase morphs and phoresy: New species of Antennoseius (Vitzthumia) mites (Acari: Mesostigmata: Ascidae) associated with pyrophilous carabids (Carabidae: Sericoda spp.) in Alberta, Canada
FIGURES 10–13. Antennoseius perseus n. sp., female, free-living form. 10, Dorsal shields; 11, Ventral shields; 12, Subcapitulum; 13, Right chelicera, lateral view.
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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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.