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Figure 2 in An interesting rare tylenchid species, Antarctenchus urmiensis n. sp. (Tylenchomorpha; Psilenchidae) from Urmia Lake islands, northwest Iran, with a discussion on the taxonomy of related genera
Figure 2: Light micrographs of ANtarCteNCHUS UrmieNSiS n. sp. (A,B,E,F,G,H,I,J,M,P,Q: Female; C,D,K,L,N,O,R: Male) (A-D) Anterior body end; (E) Anterior body region; (F) Pharyngeal median bulb; (G) Part of female reproductive system; (H) Distal end of ovary; (I) Pharyngeal bulb; (J) Lateral lines; (K) Male tail; (L) Phasmid; (M) Female tail; (N) Bursa; (O&P) Entire body; (Q) Vulval region; (R) Spicule and gubernaculum. (Scale bars: A-N, Q&R = 10 μm; O&P = 50 μm).
Fig. 4 in Classification of pleurodire polystomes (Platyhelminthes, Monogenea, Polystomatidae) revisited with the description of two new genera from the Australian and Neotropical Realms
Fig. 4. Haptor of Polystomoides brasiliensis showing the deep incisions between suckers. Scale bar = 200 μm.
Fig. 3 in Classification of pleurodire polystomes (Platyhelminthes, Monogenea, Polystomatidae) revisited with the description of two new genera from the Australian and Neotropical Realms
Fig. 3. Violin plot of the genital spines number. A = Aussietrema infecting pleurodires; B = Neopolystoma infecting pleurodires; C = Polystomoides infecting pleurodires; D = Uropolystomoides infecting pleurodires of the Australian Realm; E = Uropolystomoides infecting pleurodires of the Ethiopian Realm; F = Fornixtrema infecting cryptodires; G = Neopolystoma infecting cryptodires; G = Polystomoides infecting cryptodires; I = Uropolystomoides infecting cryptodires; J = Apalonotrema moleri infecting a cryptodire host. K = Uteropolystomoides nelsoni infecting a cryptodire host.
Fig. 1 in Classification of pleurodire polystomes (Platyhelminthes, Monogenea, Polystomatidae) revisited with the description of two new genera from the Australian and Neotropical Realms
Fig. 1. Lateroventral vaginae as observed for Neopolystoma kreffti (A), Uropolystomoides scottae (B) and Polystomoides brasiliensis (C). Annotations: gb, genital bulb; ov, ovary; te, testis; vg, vaginae. Scale bar = 200 μm.
Fig. 6 in Classification of pleurodire polystomes (Platyhelminthes, Monogenea, Polystomatidae) revisited with the description of two new genera from the Australian and Neotropical Realms
Fig. 6. Hamuli of Polystomoides spp. A = Polystomoides japonicum Ozaki, 1935; B = Polystomoides magdalenensis Lenis and Garcia-Prieto, 2009; C = Polystomoides ocellatum (Rudolphi, 1819); D = Polystomoides pauli (Timmers and Lewis, 1979); E = Polystomoides platynotae Combes and Rohde, 1979; F = Polystomoides rohdei; G = Polystomoides brasiliensis; H = Polystomoides fuquesi Man´e-Garzon and Gil, 1962; I = Polystomoides uruguayensis Man´e-Garzon and Gil, 1961. Scale bar = 50 μm.
Fig. 2 in Classification of pleurodire polystomes (Platyhelminthes, Monogenea, Polystomatidae) revisited with the description of two new genera from the Australian and Neotropical Realms
Fig. 2. Violin plot of inter-vaginal distance as % of the body width at the level of the vagina. The plot visualises the probability density of the data at different values. Within each violin is a marker for the median of the data as well as marker indicating the interquartile range. A = Aussietrema infecting pleurodires; B = Neopolystoma infecting pleurodires; C = Polystomoides infecting pleurodires; D = Uropolystomoides infecting pleurodires of the Australian Realm; E = Uropolystomoides infecting pleurodires of the Ethiopian Realm; F = Fornixtrema infecting cryptodires; G = Neopolystoma infecting cryptodires; G = Polystomoides infecting cryptodires; I = Uropolystomoides infecting cryptodires; J = Apalonotrema moleri infecting a cryptodire host. K = Uteropolystomoides nelsoni infecting a cryptodire host.
FIGURE 1 in New and little known crane-fly species of the genera Helius, Elephantomyia and Toxorhina (Diptera, Limoniidae) from Dominican and Mexican amber
FIGURE 1. Elephantomyia (Elephantomyia) grata Podenas and Poinar, 2001, No. 5546 (sex unknown). 1, a drawing of the head (reconstructed) in latero-dorsal view; 2, a schematic representation of the relation between the length of palpi (p), antenna (a), rostrum (r) and head (h); 3, a drawing of the left wing venation; and 4, a drawing of the right antenna in latero-dorsal view.
FIGURE 8 in New and little known crane-fly species of the genera Helius, Elephantomyia and Toxorhina (Diptera, Limoniidae) from Dominican and Mexican amber
FIGURE 8. Toxorhina (Ceratocheilus) mexicana n. sp., No. PI II 1870 (female). 1, a photograph of the body in lateral view; 2, a photograph of the apical part of rostrum in lateral view; and 3, a photograph of the ovipositor in latero-ventral view.
FIGURE 5 in New and little known crane-fly species of the genera Helius, Elephantomyia and Toxorhina (Diptera, Limoniidae) from Dominican and Mexican amber
FIGURE 5. Helius (Helius) oosterbroeki n. sp., No. 10189 (male). 1, a drawing of the head (reconstructed) in frontoventral view; 2, a drawing of the right antenna in fronto-dorsal view; 3, a drawing of the right palpus in fronto-ventral view; 4, a schematic representation of the relation between the length of palpi (p), antenna (a), rostrum (r) and head (h); 5, a drawing of right gonocoxite and gonostyles in ventral view; and 6, a drawing of the right wing. Abbreviation: gx, gonocoxite; ing, inner gonostylus; oug, outer gonostylus.
FIGURE 2 in New and little known crane-fly species of the genera Helius, Elephantomyia and Toxorhina (Diptera, Limoniidae) from Dominican and Mexican amber
FIGURE 2. Elephantomyia (Elephantomyia) grata Podenas and Poinar, 2001, No. 5546 (sex unknown). 1, a photograph of the body in lateral view; and 2, a photograph of the right antenna in latero-dorsal view.
FIGURE 7 in New and little known crane-fly species of the genera Helius, Elephantomyia and Toxorhina (Diptera, Limoniidae) from Dominican and Mexican amber
FIGURE 7. Toxorhina (Ceratocheilus) mexicana n. sp., No. PI II 1870 (female). 1, a drawing of the head (reconstructed) in lateral view; 2, a schematic representation of the relation between the length of palpi (p), antenna (a), rostrum (r) and head (h); 3, a drawing of the left wing venation; and 4, a drawing of the ovipositor in latero-ventral view.
FIGURE 6 in New and little known crane-fly species of the genera Helius, Elephantomyia and Toxorhina (Diptera, Limoniidae) from Dominican and Mexican amber
FIGURE 6. Helius (Helius) oosterbroeki n. sp., No. 10189 (male). 1, a photograph of the body in ventral view; 2, a photograph of the head in fronto-ventral view; and 3, a photograph of hypopygium in ventral view.
FIGURE 4 in New and little known crane-fly species of the genera Helius, Elephantomyia and Toxorhina (Diptera, Limoniidae) from Dominican and Mexican amber
FIGURE 4. Helius (Helius) neali n. sp., No. 10938 (male). 1, a photograph of the body in fronto-dorsal view; and 2, a photograph of the head in fronto-dorsal view and the part of thorax in dorsal view.
FIGURE 3 in New and little known crane-fly species of the genera Helius, Elephantomyia and Toxorhina (Diptera, Limoniidae) from Dominican and Mexican amber
FIGURE 3. Helius (Helius) neali n. sp., No. 10938 (male). 1, a drawing of the head (reconstructed) in fronto-dorsal view; 2, a schematic representation of the relation between the length of antenna (a), rostrum (r) and head (h); 3, a drawing of the left antenna in ventral view; 4, a drawing of the left wing venation; and 5, a drawing of the right gonocoxite and gonostyles in ventral view. Abbreviation: gx, gonocoxite; ing, inner gonostylus; oug, outer gonostylus.
FIGURE 1 in The genera Architipula Handlirsch, 1906 and Grimmenia Krzemiński and Zessin, 1990 (Diptera: Limoniidae) from the Lower Jurassic of England
FIGURE 1. Wing venation of Architipula seebachi (Geinitz, 1884). SGWG 122/82, holotype of A. seebachiana Handlirsch, 1906.
Confirmation of Basitarsal Compound Slit Sensilla (BCSS) in scorpion genera Chaerilus and Scorpiops (Arachnida: Scorpiones)
<p><span>Basitarsal Compound Slit Sensilla (BCSS) are a cluster of mechanosensory structures, collectively composed of striated, curved, successive slits located at the prodistal end of basitarsus, forming into a fan-shaped configuration. It can efficiently detect and amplify substrate-borne micro-vibrational signals at a certain frequency range which cause slit deformation (Wang et al., 2019), being most sensitive to surface Rayleigh waves and crucial for locating the vibration source (but requires sensilla on multiple legs) (Brownwell & Farley, 1979). This structure, to my knowledge, has only been formally reported in three species, <em>Androctonus australis </em>(Linnaeus, 1758), <em>Heterometrus silenus</em> (Simon, 1884) and <em>Smeringurus mesaensis </em>(Stahnke, 1957) (Barth & Wadepuhl, 1975; Brownwell & Farley, 1979; Wang et al., 2019). The present work constitutes an informal observation (out of curiosity) of BCSS across 3 genera, confirming its presence (with different forms) in two of those genera.</span></p> <p><span>BCSS was confidently confirmed in all <em>Scorpiops</em> and <em>Chaerilus</em> species examined (see figures on subsequent pages). There appeared to be some interspecific differences (e.g., the proximal boundary that delineates the sensillar area) within the same genus, but I have not confirmed if those differences are stable and non-overlapping (i.e., diagnostic). Sensilla are closely associated with specific ecological adaptions which shape their phenotypic configurations. One of the most famous sensilla in scorpions is the trichobothrium, which serves as an important diagnostic character for many distinct lineages. Similarly, the constellation array on the externodistal surface of pedipalp fixed finger was also found to be diagnostic in some vaejovids. It is interesting to note the different configurations of slit sensilla between genera <em>Scorpiops</em> and <em>Chaerilus</em>, where in <em>Chaerilus</em> a long, accessory slit sensillum was always present external to the main sensillar area (on or near its boundary). Occasionally, several short striations (sensilla?) were also observed on the joint tubercle between the basi- and telotarsi. Unfortunately, due to the magnification constraint: I was not able to examine genera <em>Langxie</em> and <em>Qianxie</em> (both with highly slender basitarsi); I was not able to confidently identify the striation in genus <em>Olivierus</em> albeit observing a similar depression at the same location (BCSS of the much smaller species of <em>Scorpiops</em> (<em>S. jendeki</em> and <em>S. kovariki</em>) and <em>Chaerilus</em> were even more conspicuous).</span></p>
Figures 205–211 in An overview of genera and subgenera of the Asura / Miltochrista generic complex (Lepidoptera, Erebidae, Arctiinae). Part 1. Barsine Walker, 1854 sensu lato, Asura Walker, 1854 and related genera, with descriptions of twenty new genera, ten new subgenera and a check list of taxa of the Asura / Miltochrista generic complex
Figures 205–211. Type species of genera of the Asura / Miltochrista generic complex: female genitalia.
Figures 166–173 in An overview of genera and subgenera of the Asura / Miltochrista generic complex (Lepidoptera, Erebidae, Arctiinae). Part 1. Barsine Walker, 1854 sensu lato, Asura Walker, 1854 and related genera, with descriptions of twenty new genera, ten new subgenera and a check list of taxa of the Asura / Miltochrista generic complex
Figures 166–173. Members of the Asura / Miltochrista generic complex: female genitalia. 166–171, 173 – type species of genera and subgenera.
Figures 198–204 in An overview of genera and subgenera of the Asura / Miltochrista generic complex (Lepidoptera, Erebidae, Arctiinae). Part 1. Barsine Walker, 1854 sensu lato, Asura Walker, 1854 and related genera, with descriptions of twenty new genera, ten new subgenera and a check list of taxa of the Asura / Miltochrista generic complex
Figures 198–204. Type species of genera of the Asura / Miltochrista generic complex: female genitalia.
Figures 156–159 in An overview of genera and subgenera of the Asura / Miltochrista generic complex (Lepidoptera, Erebidae, Arctiinae). Part 1. Barsine Walker, 1854 sensu lato, Asura Walker, 1854 and related genera, with descriptions of twenty new genera, ten new subgenera and a check list of taxa of the Asura / Miltochrista generic complex
Figures 156–159. Members of the Asura / Miltochrista generic complex: male genitalia. 156–158 – type species of genera.
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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.