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Figure 2 in A new species of Polypoetes Druce, 1885 (Lepidoptera: Notodontidae) from Colombia, with confirmation of a new host plant for the Dioptinae
Figure 2. Male genitalia of Polypoetes milleri spec. nov. A. Ventral. B. Dorsal. C. Lateral. D. Aedeagus. E. Sternite 8. F. Tergite 8. Scale: 1 mm. / A. Ventral. B. Dorsal. C. Lateral. D. Aedeago. E. Esternito 8. F. Terguito 8. Escala: 1 mm.
Figure 1 in A new species of Polypoetes Druce, 1885 (Lepidoptera: Notodontidae) from Colombia, with confirmation of a new host plant for the Dioptinae
Figure 1. Habitus of Polypoetes milleri spec. nov. Holotype male. A. Dorsal. B. Ventral. Paratype female. C. Dorsal. D. Ventral. Scale: 1 cm. / Holotipo macho. A. Dorsal. B. Ventral. Paratipo hembra. C. Dorsal. D. Ventral. Escala: 1 cm.
Figure 7 in Stylostome of the trombiculid mite larvaeNeotrombicula talmiensis (Schluger, 1955) (Acariformes, Trombiculidae) feeding on two host species in the Russian Far East
Figure 7 Stylostomes of Neotrombicula talmiensis(Schluger, 1955) larvae in the skin of the Asian chipmunkTamias sibiricus(Laxmann, 1769). Histological sections of aural cavity. Azure II-Eosin. A – Young stylostome composed of one eosinophil cone with the already developed feeding cavity situated within the upper epidermal layers. Note the grayish substance underneath the eosinophil cone arrow(). Scale bar – 50 μm; B – Young stylostome at the initial stage of development with the nearly empty feeding cavity underneath it. Note that the pale-grey substance
Figure 6 in Stylostome of the trombiculid mite larvaeNeotrombicula talmiensis (Schluger, 1955) (Acariformes, Trombiculidae) feeding on two host species in the Russian Far East
Figure 6 Skin injury of the Asian chipmunkTamias sibiricus(Laxmann, 1769) during feeding ofNeotrombicula talmiensis(Schluger, 1955) larvae. Histological sections of aural cavity. Azure II-Eosin. A - General view of aural cavity damaged by numerous feeding larvae. Note the differently developed stylostomes evolving within scabs. Scale bar – 500 μm; B – Two young closely disposed stylostomes evolving within epidermis. Note the numerous larvae at different feeding stages occupying the aural cavity. The feeding cavity is barely expressed. Scale bar 200 μm; C – Two young stylostomes of the recently attached larvae at different developmental stages evolving within the epidermis showing the large feeding cavity filled with numerous inflammatory cells. — car – aural cartilage, der – dermis, ec – eosinophil cone, ep – epidermis fc – feeding cavity, lar – larvae, sb – scab, st – stylostome, stc – stratum corneum
Figure 5 in Stylostome of the trombiculid mite larvaeNeotrombicula talmiensis (Schluger, 1955) (Acariformes, Trombiculidae) feeding on two host species in the Russian Far East
Figure 5 Skin injury of voles Myodes rufocanusSundevall, 1846 and stylostomes ofNeotrombicula talmiensis(Schluger, 1955) larvae. Histological sections. Azure II-Eosin. A – Several stylostomes evolving in both hypertrophic epidermis and penetrating into the strongly expressed feeding cavities filled with numerous infiltrating cells and cell debris. Note the grayish substance at the periphery of stylostomesarrows(). Scale bar – 100 μm; B – Two closely disposed stylostomes evolving within the cell association of the broken inflammatory and epidermal cells (arrows). Scale bar – 50 μm; C – Three differently arranged stylostomes evolving within the pronounced feeding cavity tightly packed with the broken inflammatory and epidermal cells fused to form a scab. Note the grayish substance at the periphery of stylostomesarrows(). Scale
Figure 4 in Stylostome of the trombiculid mite larvaeNeotrombicula talmiensis (Schluger, 1955) (Acariformes, Trombiculidae) feeding on two host species in the Russian Far East
Figure 4 Stylostomes of Neotrombicula talmiensis(Schluger, 1955) larvae in the skin of volesMyodes rufocanusSundevall, 1846. Histological sections. Azure II-Eosin. A – Young stylostome evolved in the hypertrophic stratum corneum. Note the active stratum lucidum surrounding growing stylostome and feeding cavity filled with a flocculent material without inflammatory cells. Stylostome canal is also empty. Scale bar
Figure 3 in Stylostome of the trombiculid mite larvaeNeotrombicula talmiensis (Schluger, 1955) (Acariformes, Trombiculidae) feeding on two host species in the Russian Far East
Figure 3 Skin injury of voles Myodes rufocanusSundevall, 1846 during feeding ofNeotrombicula talmiensis(Schluger, 1955) larvae. Histological sections of aural cavity. Azure II-Eosin. A – General view of aural cavity damaged by feeding larvae. Scale bar – 200 μm; B
Figure 2 in Stylostome of the trombiculid mite larvaeNeotrombicula talmiensis (Schluger, 1955) (Acariformes, Trombiculidae) feeding on two host species in the Russian Far East
Figure 2 Cheliceral blades and sites of attachment ofNeotrombicula talmiensis(Schluger, 1955) larvae. SEM. A – Cheliceral blades, dorsal view. Arrows show two small barbs on the tip of the cheliceral blades, the third barb is not visible.Arrowheadpoints to a groove on the medial surface of the cheliceral blade. Scale bar – 10 μm; B – Cheliceral blades, lateral view.Arrows indicate hardly noticeable barbs on the tip of the cheliceral blades (tricuspid cap). Scale bar – 10 μm; C – Sites of the larval attachment on the vole skin (arrows). Scale bar – 40 μm; D
Figure 1 in Stylostome of the trombiculid mite larvaeNeotrombicula talmiensis (Schluger, 1955) (Acariformes, Trombiculidae) feeding on two host species in the Russian Far East
Figure 1 Organization ofNeotrombicula talmiensis(Schluger, 1955) larvae. SEM. A – Scutum (one of sensilla broken). Scale bar – 40 μm; B – Paired eye and posterolateral seta of scutum.Arrow points to a pore on the scutal surface. Scale bar – 10 μm; C – Gnathosoma, dorsal view (palpal claws not visible). Arrows show branched setae on palpal femur, genu, and tibia (ventral seta of tibia and palpal tarsus not shown
Fig. 4 in The Role Of Different Mollusk Species In Maintaining The Transmission Of Polyhostal Trematode Species In Ukrainian Polissya Waters: The Specificity Of Trematode Parthenogenetic Generations To Mollusk Hosts
Fig. 4. The distribution of olygoxenic three-host trematode species in the parthenitae host species of mollusks: A — E. stantschinskii; B — P. ovata; C — C. cornutus; D — T. clavata.
Fig. 3 in The Role Of Different Mollusk Species In Maintaining The Transmission Of Polyhostal Trematode Species In Ukrainian Polissya Waters: The Specificity Of Trematode Parthenogenetic Generations To Mollusk Hosts
Fig. 3. The distribution of polyxenic trematode species in the parthenitae host species of mollusks: A — H. conoideum; B — E. recurvatum.
Fig. 6 in The Role Of Different Mollusk Species In Maintaining The Transmission Of Polyhostal Trematode Species In Ukrainian Polissya Waters: The Specificity Of Trematode Parthenogenetic Generations To Mollusk Hosts
Fig. 6. The distribution of olygoxenic two-host trematode species in the parthenitae host species of mollusks: A — P. ichikawai; B — D. subclavatus; C — F. hepatica; D — L. constantinovae; E — A. imitans.
Fig. 2 in The Role Of Different Mollusk Species In Maintaining The Transmission Of Polyhostal Trematode Species In Ukrainian Polissya Waters: The Specificity Of Trematode Parthenogenetic Generations To Mollusk Hosts
Fig. 2. The distribution of olygoxenic three-host trematode species in the parthenitae host species of mollusks: A — H. cylindracea; B — H. variegatus; C — E. aconiatum; D — E. revolutum.
Fig. 5 in The Role Of Different Mollusk Species In Maintaining The Transmission Of Polyhostal Trematode Species In Ukrainian Polissya Waters: The Specificity Of Trematode Parthenogenetic Generations To Mollusk Hosts
Fig. 5. The distribution of polyxenic trematode species in the parthenitae host species of mollusks: A — N. attentuatus; B — L. scotiae.
Fig. 30 in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 30 (continued on next page). Distribution of the lutko species group fritillaries in combination with the distribution of known and suspected species of host plants from the genus Phlomoides Blume. = Melitaea lutko Evans, 1932; = M. timandra timandra Coutsis & Oorschot, 2014; = M. timandra binaludica subsp. nov.; = M. shahvarica sp. nov.; = M. mimetica mimetica Higgins, 1940; = M. mimetica delerei Heidemann, 1954;? = unconfirmed findings of M. timandra; = M. timandra with an unclear subspecies status; = Phlomoides regeliana (Aitch. & Hemsl.) Adylov, Kamelin & Makhm.; = Phlomoides boissieriana (Regel) Adylov, Kamelin & Makhm.; = Phlomoides laciniata (L.) Kamelin & Makhm.; = Phlomoides labiosiformis (Popov) Adylov, Kamelin & Makhm.; = Phlomoides loasifolia (Benth.) Kamelin & Makhm.; = Phlomoides molucelloides (Bunge) Salmaki; = Phlomoides acaulis (Beck ex Rech.f.) Salmaki; = Phlomoides labiosa (Bunge) Adylov, Kamelin & Makhm. A. Pakistan, Chitral, Chaghbini CGNP, alt. 2700–3000 m. B. Pakistan, Khyber Pakhtunkhwa, Drosh. C. Pakistan, Khyber Pakhtunkhwa, Keon Nullah. D. Pakistan, Khyber Pakhtunkhwa, Malakand. E. Pakistan, Khyber Pakhtunkhwa, Birmoglasht. F. Turkmenistan, Badkhyz, Kepeli, alt. 700 m. G. Turkmenistan, Badkhyz, Kyzyl-Jar, alt. 700 m. H. Turkmenistan, Kushka, alt. 700 m. I. Turkmenistan, Murgab river, Sary-Yazy, alt. 300 m. J. Turkmenistan, 30 km E of BairamAli, Zahmet, alt. 240 m. K. Turkmenistan, Bairam-Ali, alt. 230 m. L. Turkmenistan, Kara-Kum desert, 30 km W of Mary, alt. 200 m.M. Turkmenistan, Dushak, alt. 250 m.N. Turkmenistan, Chaacha, alt. 400 m. O. Turkmenistan, Bakharden, alt. 200 m. P. Iran, Khorossan Razavi, Kuh-e-Binalud Mts, Qadamgah area, Gerina, alt. 2000 m. Q. Iran, Khorasan Razavi, Kuh-e-Binalud Mts, 15 km SW of Zoshk, alt. 2300– 2500 m. R. Iran, S Khorosan, 75 km N of Birjant, Sedeh, alt. 1500 m. S. Iran, S Khorosan, 35 km N of Birjant, alt. 1500 m. T. Afghanistan, Bamian, Band-e-Amir, Dzhudoi-Kvak Gorge, alt. 3200 m. U. Afghanistan, Bamian, Band-e-Amir, Hazarajat, alt. 3000–3200 m. V. Afghanistan, Bamian, Koh-iBaba Mts, Joshanak, alt. 2800 m. W. Afghanistan, Heart, Qala-i-Naw, Kashka pass. X. Iran, Semnan, Shahvar Mt., alt. 2200–2500 m. Y. Turkmenistan, Kara-Kala, Monjukly Ridge, 300–700 m. Z. Iran, Golestan, E Maraveh Tappeh, N Ghazan Ghayeh, Palizan Mts. A". Pakistan, Balochistan, Quetta, Urak, alt. 2500 m. B". Pakistan, Balochistan, Ziarat, alt. 2500 m. C". Pakistan, Balochistan, Khojak, alt. 1700 m. D". Pakistan, Balochistan, Zaghum, alt. 1600 m; E". Pakistan, Punjab, Gawar, alt. 500 m. F". Pakistan, Balochistan, Sheik Wazil, alt. 1600 m. G". Afghanistan, Bamian, Hushkak, alt. 2700–2800 m. H". Afghanistan, Bamian, Punjub Distr., 10 km NE of Varas, alt. 2400 m. I". Afghanistan, Ghor, 17 km E of Changcharan, 15 km S of Bandi-Ali, Gazak Mts, alt. 2400 m. J". Afghanistan, Ghor, Bayan Range, 15 km S of Changcharan, Kindival valley, alt. 2700 m. K". Afghanistan, Bamiyan, Kohi-Baba Mts, Panjao, alt. 3000 m. Afghanistan, Bamiyan, Koh-i-Baba Mts, Shah-tu-Kotal, alt. 4000 m. L". Afghanistan, Kapisa, Pandshir valley, alt. 2200–2800 m. M". Afghanistan, Kabul. N". Iran, Tehran, Elburz Ridge, Demavend Mt., Ask, alt. 1800 m. O". Iran, Semnan, Foulad Mohaleh, alt. 2200 m. P". Pakistan, Punjab, Murree.
Fig. 29 in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 29.Differences in the structure of valva and aedeagus of the lutko species group.A. Melitaea shahvarica sp. nov. B, D, H. M. timandra binaludica subsp. nov. C–E. M. mimetica Higgins, 1940. F. M. lutko Evans, 1932. G. M. timandra timandra Coutsis &van Oorschot, 2014. A. Iran, Semnan Prov., Shahrud area, S macroslope of Shahvar Mts, alt. 2200–2400 m. B. Iran, Rezavi Khorassan Prov., Kuh-e-Binalud Mts, Dorrud v. vicinity, alt. 2430 m. C. Afghanistan, Bamian Prov., Punjub Distr., 10 km NE of Varas v., alt. 2400 m. D. Afghanistan, Band-i-Amir, Hazarajat. E. Pakistan, Balochistan, Quetta, Urak, alt. 2400– 2700 m. F. Pakistan, Chitral, Gol National Park, alt. 2700 m. G. Turkmenistan, Sary-Yazy, alt. 700 m. H. Iran, Rezavi Khorassan Prov., Kuh-e-Binalud Mts, Dorrud v. vicinity, alt. 2430 m.
Fig. 28 in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 28.Eggs and caterpillars of Melitaea shahvarica sp. nov. in nature and in the laboratory.A–B. Freshly laid eggs under a leaf of a host plant, May 2018, Iran, Shahvar Mt., alt. 2200 m. C–D. IV–V instar caterpillars on the leaves of the host plant Phlomoides molucelloides (Bunge) Salmaki, July 2019, Iran, Shahvar Mt., alt. 2500 m. E. I instar caterpillars in the laboratory, Moscow, May 2018. F. VI instar caterpillars during diapause, Moscow, October 2018.
Fig. 18. Male genitalia and harpe. A–C in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 18. Male genitalia and harpe. A–C. Melitaea shahvarica sp. nov. D–E. M. lutko Evans, 1932. F–I. M. mimetica Higgins, 1940. A–C. Iran, Semnan Prov., Shahrud area, S macroslope of Shahvar Mts, alt. 2200–2400 m. D–E. Pakistan, Chitral, Chaghbini, CGNP [Chitral Gol National Park], alt. 2700 m. F–G. Afghanistan, Bamian Prov., Punjub Distr., 10 km. NE Varas v., alt. 2400 m. H–I. Afghanistan, Bamian Prov., Panjub Distr., 10 km. NE Varas vil., alt. 2400 m.
Fig. 8 in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 8. Distribution of Melitaea mimetica Higgins, 1940. For a description of the symbols with letters, see Fig. 30. = M. mimetica mimetica Higgins, 1940; = M. mimetica delerei Heidemann, 1954.
Fig. 14 in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 14. Distribution of Melitaea timandra timandra Coutsis & van Oorschot, 2014, M. timandra binaludica subsp. nov. and M. shahvarica sp. nov. For a description of the points by letters, see Fig. 30. = Melitaea timandra timandra; = Melitaea timandra binaludica subsp. nov.; = Melitaea shahvarica sp. nov.;? = unconfirmed finds of Melitaea timandra; = Melitaea timandra with uncertain subspecies status.
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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.