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Fig. 1 in An overview of the Dactylosomatidae (Apicomplexa: Adeleorina: Dactylosomatidae), with the description of Dactylosoma kermiti n. sp. parasitising Ptychadena anchietae and Sclerophrys gutturalis from South Africa
Fig. 1. (A–L). Dactylosoma kermiti n. sp. from the grass frog Ptychadena anchietae. (A–H) Primary merogony. (A) Young trophozoite. (B–D) Trophozoites. (E) Young meront. (F–G) Primary meronts. (H) Merozoites. (I–L) Secondary merogony. (I) Secondary meront. (J) Immature gamont. (K) Gamont. (L) Extracellular gamont. Arrowheads show condensed chromatin (A–I); arrows show vacuoles (B–E). All images captured from the deposited slides [NMB P 534 – 535]. Scale bar 10 μm.
Fig. 2 in An overview of the Dactylosomatidae (Apicomplexa: Adeleorina: Dactylosomatidae), with the description of Dactylosoma kermiti n. sp. parasitising Ptychadena anchietae and Sclerophrys gutturalis from South Africa
Fig. 2. (A–L). Dactylosoma kermiti n. sp. from the guttural toad Sclerophrys gutturalis. (A–D) Primary merogony. (A) Young trophozoite. (B) Trophozoites. (C) Young meront. (D–L) Secondary merogony. (D) Young secondary meront. (E) Secondary meront. (F–G) Secondary merozoites. (H–I) Gamont. (K) Extracellular gamont. (L) Secondary meront in leukocyte. Arrowheads show condensed chromatin (D–H, L); arrows show vacuoles (B) and merozoites (F–G). All images captured from the deposited slides [NMB P 536 – 537]. Scale bar 10 μm.
Fig. 3 in An overview of the Dactylosomatidae (Apicomplexa: Adeleorina: Dactylosomatidae), with the description of Dactylosoma kermiti n. sp. parasitising Ptychadena anchietae and Sclerophrys gutturalis from South Africa
Fig. 3. (A–L). Dactylosoma sp. from Pelophylax lessonae. (A–D) Primary merogony. (A) Trophozoite. (B) Young meront. (C–G) Secondary meronts. (F–H) Merozoites, arrows. (I–L) Secondary merogony. (I) Young meront. (J) Meront. (K) Merozoite. (L) Gamont. Arrowheads show condensed chromatin; arrows show vacuoles (A) and merozoites (F–H). All images captured from the deposited slide [NMB P 538]. Scale bar 10 μm.
Fig. 3 in METAPOCYRTUS MADAYAW SP. N. (COLEOPTERA: CURCULIONIDAE, ENTIMINAE), A NEW FLIGHTLESS WEEVIL FROM EASTERN MINDANAO, PHILIPPINES
Fig. 3. Metapocyrtus (Artapocyrtus) spp. A, B – M. (A.) pardalis Heller, 1912 (female paratype): A – rostrum, dorsal view, B – same, lateral view; C, D – M. (A.) madayaw sp. n.: C – rostrum, dorsal view; D – idem, lateral view.
Fig. 2 in METAPOCYRTUS MADAYAW SP. N. (COLEOPTERA: CURCULIONIDAE, ENTIMINAE), A NEW FLIGHTLESS WEEVIL FROM EASTERN MINDANAO, PHILIPPINES
Fig. 2. Metapocyrtus (Artapocyrtus) spp. A, B – M. (A.) pardalis Heller, 1912: A – female type, dorsal view, B – same, lateral view; C, D – M. (A.) madayaw sp. n.: C – female paratype, dorsal view; D – same, lateral view.
Fig. 1 in METAPOCYRTUS MADAYAW SP. N. (COLEOPTERA: CURCULIONIDAE, ENTIMINAE), A NEW FLIGHTLESS WEEVIL FROM EASTERN MINDANAO, PHILIPPINES
Fig. 1 Metapocyrtus (Artapocyrtus) madayaw sp. n. A – male holotype, dorsal view; B – female paratype, dorsal view; C – male holotype, lateral view; D – female paratype, lateral view.
Fig. 4 in METAPOCYRTUS MADAYAW SP. N. (COLEOPTERA: CURCULIONIDAE, ENTIMINAE), A NEW FLIGHTLESS WEEVIL FROM EASTERN MINDANAO, PHILIPPINES
Fig. 4. Metapocyrtus (Artapocyrtus) madayaw sp. n., aedeagus. A – dorsal view; B – lateral view; C – sternite IX in dorsal view.
FIgures 13–34 in Lychas jakli sp n (Scorpiones: Buthidae) from Indonesia
FIgures 13–34: Lychas jakli sp. n., segments of pedipalps. FIgures 13–23. Holotype male, right pedipalp. Chela, dorsal (13), eXternal (14), and ventral (15) views. Patella, dorsal (16), eXternal (17), and ventral (18) views. Pedipalp femur and trochanter, internal (19), dorsal (20), and ventral (21) views. Pedipalp chela, fiXed (22) and movable (23) fingers dentate margins. The trichobothrial pattern is indicated in Figures 14–17, 19–20 (white circles). FIgures 24–34. Paratype female, right pedipalp. Chela, dorsal (24), eXternal (25), and ventral (26) views. Patella, dorsal (27), eXternal (28), and ventral (29) views. Femur and trochanter, internal (30), dorsal (31), and ventral (32) views. Pedipalp chela, fiXed (33) and movable (34) fingers dentate margins.
FIgures 1–4 in Lychas jakli sp n (Scorpiones: Buthidae) from Indonesia
FIgures 1–4: Lychas jakli sp. n. FIgures 1–2. Holotype male, dorsal (1) and ventral (2) views. Figures 3–4. Paratype female, dorsal (3) and ventral (4) views. Scale bars: 10 mm (1–2), 10 mm (3–4).
FIgures 35–42 in Lychas jakli sp n (Scorpiones: Buthidae) from Indonesia
FIgures 35–42: Lychas jakli sp. n. FIgures 35, 37–39. Holotype male, telson lateral (35), metasoma and telson, lateral (37), dorsal (38) and ventral (39). Figures 36, 40–42. Paratype female, telson lateral (36), metasoma and telson, lateral (40), dorsal (41) and ventral (42). Scale bars: 10 mm (37–39), 10 mm (40–42).
FIgures 5–12 in Lychas jakli sp n (Scorpiones: Buthidae) from Indonesia
FIgures 5–12. Lychas jakli sp. n. FIgures 5–6, 9–12. Holotype male, carapace and tergites I–IV (5), sternopectinal region and sternites (6), and left legs I–IV, retrolateral aspect. Figures 7–8. Paratype female, carapace and tergites I–III (7), sternopectinal region and sternites (8).
Figure 4 in Morphology and phylogeny of a new soil ciliate, Colpodidium zelihayildizae n. sp. (Ciliophora, Nassophorea, Colpodidiidae), from Van, Turkey
Figure 4. Alignment of the SSU-rDNA sequences of C. caudatum (EU264560) and C. zelihayildizae n. sp. (MW411350) to show the substitution positions.
Figure 3 in Morphology and phylogeny of a new soil ciliate, Colpodidium zelihayildizae n. sp. (Ciliophora, Nassophorea, Colpodidiidae), from Van, Turkey
Figure 3. Microphotographs of C. zelihayildizae n. sp. with silver carbonate staining (a–f): a, b: Ventral ciliature of representative individuals. c: Dorsal ciliature of representative individual. d, e: Oral ciliature to show paroral membranelle, NO1 and NO3, and postoral kineties 1−4. f: Oral ciliature to show NO2 and NO3. Arrowheads in Figure d show the dikinetidal section of K1. Cyt: cytopyge, EP: excretory pore, K1: the kinety on the right side of oral apparatus, Ma: macronucleus, NO1−NO3: nassulid organelles 1−3, PM: paroral membrane, PO1−PO4: postoral kinety 1−4, Arrowheads in figure d show dikinetidal section of K1.
Figure 2 in Morphology and phylogeny of a new soil ciliate, Colpodidium zelihayildizae n. sp. (Ciliophora, Nassophorea, Colpodidiidae), from Van, Turkey
Figure 2. Micropotographs of C. zelihayildizae n. sp. live (a–d) and silver nitrate-stained (e−f). BC: buccal cavity, CV: contractile vacuole, Ma: macronucleus, NO2: nassulid organelle 2, NO3: nassulid organelle 3, PM: paroral membranelle. Arrowheads show the furrowed edge of the antero-ventral surface. Scale bars 20 mm.
Figure 1 in Morphology and phylogeny of a new soil ciliate, Colpodidium zelihayildizae n. sp. (Ciliophora, Nassophorea, Colpodidiidae), from Van, Turkey
Figure 1. Morphology, infraciliature, and cortical structure of C. zelihayildizae n. sp. live (a– d), and silver nitrate- and silver carbonatestained (f–j). a: Ventral view of a representative individual. b–d: Left lateral, right lateral, and dorsal view, respectively, to show general body outline, buccal cavity, contractile vacuole, and nuclear localization. e: Part of the pellicle to show silverline system. f, g: Infraciliature in ventral (f) and dorsal view (g). h, i: Oral ciliature in different focal levels. BC: buccal cavity, CV: contractile vacuole, Cyt: cytopyge, DK: dikinetid part of K1, EP: excretory pore, K1: the kinety on the right side of oral apparatus, Ma: macronucleus, Mi: micronucleus, NO1−NO3: nassulid organelles 1−3, PM: paroral membrane, PO1−PO4: postoral kinety 1−4. Small arrows (h, i) show dikinetids above the excretory pore. Scale bars 20 mm.
Figure 5 in Morphology and phylogeny of a new soil ciliate, Colpodidium zelihayildizae n. sp. (Ciliophora, Nassophorea, Colpodidiidae), from Van, Turkey
Figure 5. Phylogenetic tree obtained from SSU rRNA gene sequences analyses using ML and BI methods to show the position of C. zelihayildizae (in red and bold). The numbers on the nodes represent the bootstrap values of the ML analysis and posterior probabilities of BI analysis, respectively. Full support in both analyses (100% ML and 1.00 BI) is marked with a bold circle. The scale bar indicates 9 substitutions per 100 nucleotide positions.
РИС. 3. Пенисы моллюсков сем. Bithyniidae иЗ водоемов Тюменской области. A. Bithynia tentaculata, B. B. decipiens, C. B. curta, D. B. producta, E. Boreoelona contortrix, F.Opisthorchophorus troscheli, G. O. baudonianus, H. O. abakumovae, I. Boreoelona sibirica, J. Paraelona socialis, K. P. milachevitchi, L. Digyrcidum bourguignati, M. Boreoelona sp., N. Digyrcidum starobogatovi. МасШтабнаЯ линейка 1 мм. Фото: Н.И. Андреев. FIG. 3. The penes of the bithyniid species from Tyumen Region. A. Bithynia tentaculata, B. B. decipiens, C. B. curta, D. B. producta, E. Boreoelona contortrix, F.Opisthorchophorus troscheli, G. O. baudonianus, H. O. abakumovae, I. Boreoelona sibirica, J. Paraelona socialis, K. P. milachevitchi, L. Digyrcidum bourguignati, M. Boreoelona sp., N. Digyrcidum starobogatovi. Scale bars: 1 mm. Photos: N.I. Andreyev. in Моллюски семейства Bithyniidae (Mollusca, Gastropoda) Тюменской области
РИС. 3. Пенисы моллюсков сем. Bithyniidae иЗ водоемов Тюменской области. A. Bithynia tentaculata, B. B. decipiens, C. B. curta, D. B. producta, E. Boreoelona contortrix, F.Opisthorchophorus troscheli, G. O. baudonianus, H. O. abakumovae, I. Boreoelona sibirica, J. Paraelona socialis, K. P. milachevitchi, L. Digyrcidum bourguignati, M. Boreoelona sp., N. Digyrcidum starobogatovi. МасШтабнаЯ линейка 1 мм. Фото: Н.И. Андреев. FIG. 3. The penes of the bithyniid species from Tyumen Region. A. Bithynia tentaculata, B. B. decipiens, C. B. curta, D. B. producta, E. Boreoelona contortrix, F.Opisthorchophorus troscheli, G. O. baudonianus, H. O. abakumovae, I. Boreoelona sibirica, J. Paraelona socialis, K. P. milachevitchi, L. Digyrcidum bourguignati, M. Boreoelona sp., N. Digyrcidum starobogatovi. Scale bars: 1 mm. Photos: N.I. Andreyev.
Table 3 b in Description of Epistylis camprubii n. sp., a Species Highly Tolerant to Ammonium and Nitrite
<p><b>Table 3b.</b> Comparison between <i>Epistylis camprubii</i> and the other <i>Epistylis</i> species mentioned in the manuscript: characteristics of stalk, macronucleus and contractile vacuole.</p><table><tbody><tr><th>Species</th><th>Stalk width <i>in vivo</i> (µm)</th><th>Stalk striation / segmentation</th><th>Macronucleus</th><th>Contractile vacuole</th><th>Data source</th></tr></tbody><tbody><tr><th><i>Epistylis camprubii</i></th><td>3.1–8.4</td><td>Longitudinally striated, occasionally transeverse segmentation</td><td>C-shaped, transversely oriented; adoral half of the body</td><td>1, adoral third of the body, on dorsal wall of vestibulum</td><td>Present manuscript</td></tr><tr><th><i>E. balatonica</i></th><td>–</td><td>Longitudinally finely striated</td><td>Horinzotal horsehoe-shaped in the middle of the body</td><td>1, in the heigh of the peristomial lip</td><td>Stiller 1971</td></tr><tr><th><i>E. chrysemydis</i></th><td>13–25</td><td>Longitudinally striated, occasionally transeverse segmentation</td><td>C-shaped, transversely oriented; adoral half of the body</td><td>1, close or in the heigh of the peristomial lips, on ventral wall of vestibulum</td><td>Foissner <i>et al</i>. 1992</td></tr><tr><th><i>E. coronata</i></th><td>11–18</td><td>–</td><td>Semicircular, adoral half of the body</td><td>1, in the height of the peristomial lips, on dorsal wall of vestibulum</td><td>Foissner <i>et al</i>. 1992</td></tr><tr><th><i>E. entzii</i></th><td>18</td><td>–</td><td>3/4 circular, adoral half of the body</td><td>1, in the heigh of the peristomial lip, on dorsal wall of vestibulum</td><td>Foissner <i>et al</i>. 1992</td></tr><tr><th><i>E. epistyliformis</i></th><td>–</td><td>Transverse segmentation</td><td>Intenselly flattened, horsehoe-shaped</td><td>1, adoral third of the body</td><td>Stiller 1971</td></tr><tr><th><i>E. hentscheli</i></th><td>12–20, sometimes 25</td><td>Occasionally finely annulated</td><td>Semicircular, adoral half of the body</td><td>1, in the heigh of the peristomial lip, on ventral wall of vestibulum</td><td>Foissner <i>et al</i>. 1992</td></tr><tr><th><i>E. plicatilis</i></th><td>7–18</td><td>Longitudinally finely striated</td><td>Semicircular, adoral half of the body</td><td>1, in the heigh of the peristomial lip, on dorsal wall of vestibulum</td><td>Foissner <i>et al.</i> 1992</td></tr><tr><th><i>E. rotans / E. procumbens</i></th><td>–</td><td>Fine longitudinally striated, transverse segmentation</td><td>Reniform to semicircular, in transverse axis and adoral half of zooid</td><td>1, at level of peristomial lip, on dorsal wall Foissner <i>et al</i>. 1999 of vestibulum</td></tr><tr><th><i>E. rotans</i></th><td>–</td><td>Longitudinally striated, transeverse segmentation</td><td>C-shaped, transversely oriented, adoral third of the body</td><td>1, located in the adoral third of the body</td><td>Curds 1969</td></tr><tr><th><i>E. thienemanni</i></th><td>–</td><td>–</td><td>Flattened ribbon-like and horsehoe-shaped, adoral third of the body</td><td>1, located in the peristomial disc, on dorsal wall of vestibulum</td><td>Stiller 1971</td></tr><tr><th><i>E. variabilis</i></th><td>Variable</td><td>–</td><td>–</td><td>1, at the level of the peristomial lip</td><td>Stiller 1971</td></tr></tbody></table>
Table 3 a in Description of Epistylis camprubii n. sp., a Species Highly Tolerant to Ammonium and Nitrite
<p><b>Table 3a.</b> Comparison between <i>Epistylis camprubii</i> and the other <i>Epistylis</i> species mentioned in the manuscript: characteristics of zooid and persitome.</p><table><tbody><tr><th>Species</th><th>Body lenght <i>in vivo</i> (µm)</th><th>Body width <i>in vivo</i> (µm)</th><th>Zooid shape</th><th>Peristomial disc diameter <i>in vivo</i> (µm)</th><th>Peristomial disc shape</th><th>Peristomial lip height <i>in vivo</i> (µm)</th><th>Peristomial lip width <i>in vivo</i> (µm)</th><th>Number of peristomial lips</th><th>Data source</th></tr></tbody><tbody><tr><th><i>Epistylis camprubii</i></th><td>35.3–98.1</td><td>18.0–65.2</td><td>Vase-shaped</td><td>11.2–21.3</td><td>Rounded, pointed, rarely umbilicated</td><td>5.0–10.6</td><td>16.2–31.7</td><td>1</td><td>Present manuscript</td></tr><tr><th><i>E. balatonica</i></th><td>90–100</td><td>45–55</td><td>Vase-shaped</td><td>–</td><td>–</td><td>–</td><td>–</td><td>2</td><td>Stiller 1971</td></tr><tr><th><i>E. chrysemydis</i></th><td>120–220</td><td>60–110</td><td>Vase-shaped</td><td>–</td><td>Umbilicated</td><td>–</td><td>50–80</td><td>2</td><td>Foissner <i>et al</i>. 1992</td></tr><tr><th><i>E. coronata</i></th><td>70–120</td><td>–</td><td>Vase-shaped</td><td>–</td><td>Slightly umbilicated and oblique</td><td>–</td><td>32–65</td><td>1</td><td>Foissner <i>et al</i>. 1992</td></tr><tr><th><i>E. entzii</i></th><td>125–190</td><td>80</td><td>Cylindrical</td><td>–</td><td>Convex, slightly oblique</td><td>–</td><td>–</td><td>1</td><td>Foissner <i>et al</i>. 1992</td></tr><tr><th><i>E. epistyliformis</i></th><td>43–62</td><td>20–27</td><td>Vase-shaped</td><td>–</td><td>Convex, sometimes – conical</td><td>–</td><td>1</td><td>Stiller 1971</td></tr><tr><th><i>E. hentscheli</i></th><td>110–170</td><td>38–60</td><td>Asymmetric and bell-shaped, narrowed down to the stem</td><td>–</td><td>Convex, slightly oblique</td><td>–</td><td>–</td><td>1</td><td>Foissner <i>et al</i>. 1992</td></tr><tr><th><i>E. plicatilis</i></th><td>90–160</td><td>25–50</td><td>Funnel-shaped</td><td>–</td><td>Not umbilicated</td><td>–</td><td>36–60</td><td>1</td><td>Foissner <i>et al</i>. 1992</td></tr><tr><th><i>E. rotans / E. procumbens</i></th><td>60–140</td><td>2–2½ times as long as wide</td><td>Irregular (sigmoidal – shape, bent at right</td><td>Flat or slightly convex, slightly</td><td>–</td><td>–</td><td>1</td><td>Foissner <i>et al.</i> 1999</td></tr><tr><th></th><td></td><td></td><td>angles, slightly tilted backwards)</td><td>oblique</td><td></td><td></td><td></td><td></td></tr><tr><th><i>E. rotans</i></th><td>70–100</td><td>–</td><td>Vase-shaped</td><td>–</td><td>Arched</td><td>–</td><td>–</td><td>1</td><td>Curds 1969</td></tr><tr><th><i>E. thienemanni</i></th><td>67–120</td><td>–</td><td>Vase-shaped</td><td>–</td><td>Conical</td><td>–</td><td>–</td><td>1</td><td>Stiller 1971</td></tr><tr><th><i>E. variabilis</i></th><td>50–100</td><td>–</td><td>Funnel-shaped</td><td>–</td><td>Slightly convex and obliquely protuberant</td><td>–</td><td>–</td><td>1</td><td>Stiller 1971</td></tr></tbody></table>
FIG. 3 in A new species, Lochriea monocarinata n. sp., and its position in the morphospace of the genus Lochriea Scott, 1942 (Conodonta, Mississippian)
FIG. 3. — Morphology of the P1 element of Lochriea Scott, 1942 and the terms for the orientation of the elements (Purnell et al. 2000).
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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
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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
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