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2,196 results for “Water mites”
Figure 4 Atractides manasi n in A checklist of the water mites of Central Asia with description of six new species (Acari, Hydrachnidia) from Kyrgyzstan
Figure 4 Atractides manasi n. sp., female holotype: A – idiosoma, dorsal view; B – idiosoma, ventral view; C – genital field; D – I-L-5 and -6; E – palp, medial view; F – palp, lateral view. Scale bars = 100 μm.
Figure 3 in A checklist of the water mites of Central Asia with description of six new species (Acari, Hydrachnidia) from Kyrgyzstan
Figure 3 Atractides grigorievkan. sp., female holotype: A – idiosoma, ventral view; B – genital field; C – palp, lateral view; D – palp, medial view; E – I-Leg; F – I-L-5 and -6; G – sword setae (S-1 and -2) at the ventrodistal margin of I-L-5. Scale bars = 100 μm.
Figure 2 A in First evidence of parasitation of a Bosmina (Cladocera) by a water mite larva in a karst sinkhole, in Quintana Roo (Yucatán Peninsula, México)
Figure 2 A – Lateral view of the Unionicola larva, frontal view on the Bosmina. B – Close up of perforations made by pedipalps and chelicerae of the water mite in the valve of the water flea. Scale bars indicate 50 μm.
Figure 1 Wandesia albertii n in A checklist of the water mites of Central Asia with description of six new species (Acari, Hydrachnidia) from Kyrgyzstan
Figure 1 Wandesia albertii n. sp., female holotype: A – coxal and genital field; B – palp, medial view; C – palp, lateral view; D – chelicere; E – acetabula (Ac-1-3, from left to right); F – I-Leg; G – II-Leg; H – III-Leg; I – IV-Leg. Scale = 100 μm.
Figure 1. A-B, E in First record of the halobiontic Diplodontus semiperforatus (Acari, Hydrachnidia) from North Khorasan, with notes on water mites from saline habitats of Iran
Figure 1. A-B, E: Diplodontus semiperforatus (Walter, 1925), ♀, Qareh Ghan, Iran – A. Palp, lateral view; B. Chelicera; E. Photograph of genital field. C–D: Diplodontus scapularis Dugès, 1834, Messoussate, Morocco (C – ♀, F – ♂) – C. Chelicera; D. Photograph of genital field. F. Maximum Likelihood tree (GTR+I model) of the genus Diplodontus obtained from 6 nucleotide COI sequences.
Figure 2 in First record of the halobiontic Diplodontus semiperforatus (Acari, Hydrachnidia) from North Khorasan, with notes on water mites from saline habitats of Iran
Figure 2. Photograph of sampling site (Qareh Ghan, North Khorasan Province) of Diplodontus semiperforatus in northeastern Iran. Photo by V. Pešić.
Figure 3 in Synonymy of the water mite subgenera Orientmomonia and Kondia in the genus Momonia (Momoniidae, Acari): an evaluation based on morphology and molecular data
Figure 3 Male of Momonia(Orientmomonia) koreana. A – dorsal view of idiosoma; B – ventral view of idiosoma; C – left palp; D – I-L-1–6. E – IV-L-3–6. Scale bars: 100 μm.
Figure 5 in Synonymy of the water mite subgenera Orientmomonia and Kondia in the genus Momonia (Momoniidae, Acari): an evaluation based on morphology and molecular data
Figure 5 Maximum-likelihood phylogenetic tree based on the mitochondrial cytochrome oxidase subunit I (COI) gene sequences obtained for a set ofMomoniaspecimens. Bootstrap values (> 50%) related to the nodes are indicated (1,000 replicates).
Figure 1 in Synonymy of the water mite subgenera Orientmomonia and Kondia in the genus Momonia (Momoniidae, Acari): an evaluation based on morphology and molecular data
Figure 1 Provenance of the material used in the present study. Collection site A – Tatsuno City in Hyogo Prefecture; Collection site B – Aioi City in Hyogo Prefecture; Collection site C – Tsushima City in Nagasaki Prefecture.
Figure 4 in Synonymy of the water mite subgenera Orientmomonia and Kondia in the genus Momonia (Momoniidae, Acari): an evaluation based on morphology and molecular data
Figure 4 Female of Momonia(Kondia) sp. A – dorsal view of idiosoma; B – ventral aspect of unmounted specimen; C – ventral view of idiosoma; D – right palp; E – I-L-1–6; F – IV-L-3–6. Scale bars: 100 μm.
Figure 1 Neumania australica n in The water mite genusNeumania Lebert, 1879 in Australia (Acari: Hydrachnidia
Figure 1 Neumania australica n. sp., A – D holotype male, E paratype female. A = venter male; B = palp, C = III-leg-4 – 6; D = IV=leg=5 – 6; E = genital field female. Scale bars: A, E = 100 µm, B – D = 50 µm.
Figure 4 in A new water mite species of the genus Teutonia Koenike, 1889 from Corsica, France, based on morphological data and DNA barcodes (Acari, Hydrachnidia, Teutoniidae)
Figure 4 Teutonia corsicanasp. nov., ♂ [CCDB 38559 F09], Ruisseau de Battesta, France: A – coxal and genital field, partial view; B – photograph of ejaculatory complex; C – palp, medial view; D – gnathosoma. Scale bars = 100 μm.
Figure 2 in A new water mite species of the genus Teutonia Koenike, 1889 from Corsica, France, based on morphological data and DNA barcodes (Acari, Hydrachnidia, Teutoniidae)
Figure 2 Results of ASAP analysis for COI sequences. (A) Distribution of pairwise differences, (B) Ranked pairwise differences.
Figure 1 in A new water mite species of the genus Teutonia Koenike, 1889 from Corsica, France, based on morphological data and DNA barcodes (Acari, Hydrachnidia, Teutoniidae)
Figure 1 Neighbour-Joining tree of the genusTeutonia, obtained from 17 nucleotide COI sequences.and the results of species delimitation analyses. Values near branches show bootstrap support (BS). The results of species delimitation by ASAP procedure are indicated by vertical bars. Country codes (alpha-2 code): DE – Germany, FR – France, MN – Montenegro, NO – Norway, TR – Turkey.
Figure 3 in A new water mite species of the genus Teutonia Koenike, 1889 from Corsica, France, based on morphological data and DNA barcodes (Acari, Hydrachnidia, Teutoniidae)
Figure 3 Teutonia corsicanasp. nov. (A-B, D-G – holotype ♀, Ruisseau de Tuara, France; C – ♀ [CCDB 38559 D12], preserved specimen, Riviere La Solenzara, France): A – coxal and genital field; B, C – genital field; D – palp, medial view (P-1 lacking); E – palp, lateral view; F – I-L-5 and -6; G – IV-L-5 and -6. Scale bars = 100 μm.
Figure 5 in A new water mite species of the genus Teutonia Koenike, 1889 from Corsica, France, based on morphological data and DNA barcodes (Acari, Hydrachnidia, Teutoniidae)
Figure 5 Teutonia cometes(Koch, 1837), ♀, Danilovgrad, spring under the bridge over the Zeta river, Montenegro: A – genital field; B – palp, medial view. Scale bar = 100 μm.
Figure 6 Collection sites. A in Water mites of the genusLebertia Neuman, 1880 from the eastern Himalayas (Acari: Hydrachnidia: Lebertiidae)
Figure 6 Collection sites. A – Haa River (Bhutan 03); B – Sertu Khola, Nunthala (Nepal 06); C – Garden stream, Nunthala (Nepal 05); D – Surke Khola (Nepal 04); E – stream S of Gokyo (Nepal 01); F – stream Dudh Kosi Nadi (Nepal 02). Authors: W. Klein (A), P.V. Veel (B-F).
Figure 3 in Water mites of the genusLebertia Neuman, 1880 from the eastern Himalayas (Acari: Hydrachnidia: Lebertiidae)
Figure 3 Lebertia(Lebertia) disparilisn. sp.., type series, ♂; A – coxal and genital field (partial view); B – right palp lateral; C – I-L-4-6; D – IV-L-4-6. Scale bars: 100 µm.
Figure 2 in Water mites of the genusLebertia Neuman, 1880 from the eastern Himalayas (Acari: Hydrachnidia: Lebertiidae)
Figure 2 Lebertia(Lebertia) khatriin. sp., type series. A-D, ♂; A – I-L-4-5; B – IV-L-4-6; C – right palp medial; D – coxal and genital field; E – ♀ genital. Scale bars: 100 µm.
Figure 1 in Water mites of the genusLebertia Neuman, 1880 from the eastern Himalayas (Acari: Hydrachnidia: Lebertiidae)
Figure 1 Lebertia(Lebertia) himalayaensisn. sp., type series. A-D, ♂; A – venter; B – gnathosoma with left palp and chelicera in situ; C – right palp medial; D – IV-L-3-6; E – ♀ genital field. Scale bars: 100 µm.
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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