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983 results for “Lice”

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dryad32/100

Data from: Integrating phylogenomic and population genomic patterns in avian lice provides a more complete picture of parasite evolution

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publicOct 2017View details →
dryad32/100

Data from: Phylogenomics using target-restricted assembly resolves intra-generic relationships of parasitic lice (Phthiraptera: Columbicola)

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publicMar 2017View details →
dryad32/100

Salmon louse infestation levels on sea trout can be predicted from a hydrodynamic lice dispersal model

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publicJan 2022View details →
dryad32/100

The response of avian chewing lice (Psocodea: Phthiraptera) loads to early-1900s urbanization in the Western United States

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publicMay 2025View details →
dryad32/100

Psocodea Phylogenomic dataset from: Phylogenomics of parasitic and non-parasitic lice (Insecta: Psocodea): combining sequence data and Exploring compositional bias solutions in Next Generation Datasets

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publicSep 2020View details →
dryad32/100

Data from: Effects of 16S rDNA sampling on estimates of the number of endosymbiont lineages in sucking lice

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publicJun 2017View details →
dryad32/100

Data from: Biogeography and host-related factors trumps parasite life-history: limited congruence among the genetic structures of specific ectoparasitic lice and their rodent hosts

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publicJul 2013View details →
dryad32/100

Data from: Size matters for lice on birds: coevolutionary allometry of host and parasite body size

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publicNov 2016View details →
zenodo28/100

Fig. 3 in Gallancyra gen. nov. (Phthiraptera: Ischnocera), with an overview of the geographical distribution of chewing lice parasitizing chicken

Fig. 3. Geographical distribution of four species of menoponid chewing lice parasitizing wild and domestic chicken (Gallus spp.). Each circle is divided into four sectors, representing the four louse species: upper left = Menacanthus cornutus (Schömmer, 1913); upper right = Menacanthus stramineus (Nitzsch, 1818); lower left = Menacanthus pallidulus (Neumann, 1912); lower right = Menopon gallinae (Linnaeus, 1758). Black sectors indicate that this louse species is known from this country, whereas hollow sectors indicate that we have found no published records of this species in this country. The presence of the four species of chewing lice in a country is based on the reports summarized in Table 1. Note that the menoponid species Amyrsidea powelli (Bedford, 1920) appears to be established on chicken in Nigeria (Fabiyi 1986, 1996), and that Menacanthus longiscleritus Naz & Rizvi, 2016, has been described from chicken in Pakistan. These are not shown on the map.

opencc-by-4.0Jul 2020View details →
zenodo28/100

Figs 7–8 in Gallancyra gen. nov. (Phthiraptera: Ischnocera), with an overview of the geographical distribution of chewing lice parasitizing chicken

Figs 7–8. Gallancyra dentata (Sugimoto, 1934) gen. et comb. nov. ex Gallus gallus (Linnaeus, 1758) (NHMUK010682393). 7. Male subgenital plate and terminal end of abdomen, ventral view. 8. Female subgenital plate and terminal end of abdomen, ventral view. Abbreviations: vms = vulval marginal setae; vss = vulval submarginal setae.

opencc-by-4.0Jul 2020View details →
zenodo28/100

Fig. 1 in Gallancyra gen. nov. (Phthiraptera: Ischnocera), with an overview of the geographical distribution of chewing lice parasitizing chicken

Fig. 1. Geographical distribution of three species of ischnoceran chewing lice parasitizing wild and domestic chicken (Gallus spp). Each circle is divided into three sectors, representing the three louse species: upper left = Goniodes gigas (Taschenberg, 1879); upper right = Goniodes dissimilis Denny, 1842; lower = Goniocotes gallinae (De Geer, 1778). Black sectors indicate that this louse species is known from this country, whereas hollow sectors indicate that we have found no published records of this species in this country. Presence of the three species of chewing lice in a country is based on the reports summarized in Table 1.

opencc-by-4.0Jul 2020View details →
zenodo28/100

Figs 5–6 in Gallancyra gen. nov. (Phthiraptera: Ischnocera), with an overview of the geographical distribution of chewing lice parasitizing chicken

Figs 5–6. Gallancyra dentata (Sugimoto, 1934) gen. et comb. nov. ex Gallus gallus (Linnaeus, 1758) (NHMUK010682393). 5. Habitus, ♂, dorsal and ventral view. 6. Habitus, ♀, dorsal and ventral views. Legs II and III distorted in all examined males, here illustrated approximately, and rotated compared to how they are in the slide specimen.

opencc-by-4.0Jul 2020View details →
zenodo28/100

Fig. 4 in Gallancyra gen. nov. (Phthiraptera: Ischnocera), with an overview of the geographical distribution of chewing lice parasitizing chicken

Fig. 4. Geographical distribution of the known records of Gallancyra dentata (Sugimoto, 1934), based on the reports cited in Table 1. Black circles indicate countries where G. dentata has been reported at in at least one survey, including the present report. Hollow circles indicate countries for which surveys of domestic chicken have been published, but G. dentata has not been found. In addition to the areas indicated on the map, Emerson (1956) reported G. dentata from "various islands in the Central Pacific Area", but gave no detail.

opencc-by-4.0Jul 2020View details →
zenodo28/100

Fig. 14 in Gallancyra gen. nov. (Phthiraptera: Ischnocera), with an overview of the geographical distribution of chewing lice parasitizing chicken

Fig. 14. Gallancyra dentata (Sugimoto, 1934) gen. et comb. nov. ex Gallus gallus (Linnaeus, 1758) (NHMUK010682393). Male legs I–III, dorsal and ventral views. Legs II and III distorted in all examined males, and here illustrated approximately; note that marginal and near-marginal setae (marked with small black circles) are illustrated on both dorsal and ventral side, as their exact placement is difficult to establish due to the distortion of the legs. Some setae on tibiae II–III appear hyaline in examined specimens, and have here been illustrated as hollow.

opencc-by-4.0Jul 2020View details →
zenodo28/100

Figure 4 in Composition and distribution patterns of chewing lice of two neotropical species of Turdus

Figure 4. Influence of body length variation of Turdus amaurochalinus (n = 36) and Turdus rufiventris (n = 53) on the abundance of chewing lice in three areas of Atlantic Forest, in southern Brazil, between July 2009 and June 2010.

opencc-by-4.0Aug 2014View details →
zenodo28/100

Figure 2 in Composition and distribution patterns of chewing lice of two neotropical species of Turdus

Figure 2. Infrapopulation size of Myrsidea sp. on Turdus amaurochalinus (n = 36) and Turdus rufiventris (n = 53), in three areas of Atlantic Forest, in southern Brazil, between July 2009 and June 2010.

opencc-by-4.0Aug 2014View details →
zenodo28/100

Figure 1 in Composition and distribution patterns of chewing lice of two neotropical species of Turdus

Figure 1. Infrapopulation size of all species of chewing lice and their corresponding distribution on Turdus amaurochalinus (n = 36) and Turdus rufiventris (n = 53), in three areas of Atlantic Forest, in southern Brazil, between July 2009 and June 2010.

opencc-by-4.0Aug 2014View details →
zenodo28/100

Figure 3 in Composition and distribution patterns of chewing lice of two neotropical species of Turdus

Figure 3. Infrapopulation size of Brueelia persimilis on Turdus amaurochalinus (n = 36) and Brueelia addoloratoi on Turdus rufiventris (n = 53), in three areas of Atlantic Forest, in southern Brazil, between July 2009 and June 2010.

opencc-by-4.0Aug 2014View details →
zenodo28/100

Figure 5 from: Burckhardt D, Dalle Cort G, Queiroz DL (2020) Jumping plant lice of the genus Aphalara (Hemiptera, Psylloidea, Aphalaridae) in the Neotropics. ZooKeys 980: 119-140. https://doi.org/10.3897/zookeys.980.56807

Figure 5 Forewing of Aphalara spp. A–D, I, JAphalara ortegaesp. nov. E–H, M, NAphalara ritterisp. nov. K, LAphalara persicariaCaldwell A, B, E, F, I, K, M male C, D, G, H, J, L, N female A, C, E, G venation B, D, F, H surface spinules I–N details of surface spinules. Scale bars: 0.5 mm (A–H); 0.2 mm (I–N).

opencc-by-4.0Nov 2020View details →
zenodo28/100

Figure 4 from: Burckhardt D, Dalle Cort G, Queiroz DL (2020) Jumping plant lice of the genus Aphalara (Hemiptera, Psylloidea, Aphalaridae) in the Neotropics. ZooKeys 980: 119-140. https://doi.org/10.3897/zookeys.980.56807

Figure 4 Head of Aphalara spp. A, CAphalara ortegaesp. nov. B, DAphalara ritterisp. nov. A, B dorsal view C, D ventral view. Scale bar: 0.1 mm.

opencc-by-4.0Nov 2020View details →

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Allen Brain Atlas

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Last verified 2026-04-30Open record

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behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
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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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

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