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Figures 1-6 from: Zonstein SI, Marusik YM (2017) Descriptions of the two-eyed African spider genera Chedimanops gen. n. and Hybosidella gen. n. (Araneae, Palpimanidae, Chediminae). African Invertebrates 58(1): 23-47. https://doi.org/10.3897/AfrInvertebr.58.11448
Figures 1-6 - Habitus of Chedimanops eskovi sp. n. (1–3) and Chedimanops rwenzorensis sp. n. (4–6). 1, 4 female dorsal 2, 5 female ventral 3, 6 male dorsal.
Figures 42-48 from: Zonstein SI, Marusik YM (2017) Descriptions of the two-eyed African spider genera Chedimanops gen. n. and Hybosidella gen. n. (Araneae, Palpimanidae, Chediminae). African Invertebrates 58(1): 23-47. https://doi.org/10.3897/AfrInvertebr.58.11448
Figures 42-48 - Somatic morphology of Hybosidella etinde sp. n. 42 habitus, dorsal 43 prosoma and anterior part of abdomen, ventral 44 mouth parts, ventral 45 prosoma, lateral 46–48 prosoma, ventral, antero-dorsal and dorsal. Abbreviations: Ee extention of epigastric scutum; Ms median suture; PsL paired lateral scutum. Scale bar: 0.2 mm if not otherwise indicated.
Figures 36-41 from: Zonstein SI, Marusik YM (2017) Descriptions of the two-eyed African spider genera Chedimanops gen. n. and Hybosidella gen. n. (Araneae, Palpimanidae, Chediminae). African Invertebrates 58(1): 23-47. https://doi.org/10.3897/AfrInvertebr.58.11448
Figures 36-41 - Somatic morphology of Chedimanops eskovi sp. n. (36–38), Chedimanops rwenzorensis sp. n. (39) and Hybosidella etinde sp. n. (40–41). 36, 39 female epigastral scutum, ventral; 37 male epigastral scutum, ventral; 38 male habitus, ventral; 40 tarsus I, prolateral; 41 male habitus, lateral. Abbreviations: Ee extention of epigastric scutum; PsL paired lateral scutum; PsM paired median scutum; Re receptacle. Scale bar: 0.2 mm if not otherwise indicated.
Figures 64-66 from: Zonstein SI, Marusik YM (2017) Descriptions of the two-eyed African spider genera Chedimanops gen. n. and Hybosidella gen. n. (Araneae, Palpimanidae, Chediminae). African Invertebrates 58(1): 23-47. https://doi.org/10.3897/AfrInvertebr.58.11448
Figures 64-66 - Male palp of Hybosidella etinde sp. n. 64 prolateral 65 retrolateral 66 antero-ventral. Abbreviations: Am accompanying membrane; Bl barbed tip of accompanying membrane; Cp claw-shaped process; Em embolus.
Figures 55-63 from: Zonstein SI, Marusik YM (2017) Descriptions of the two-eyed African spider genera Chedimanops gen. n. and Hybosidella gen. n. (Araneae, Palpimanidae, Chediminae). African Invertebrates 58(1): 23-47. https://doi.org/10.3897/AfrInvertebr.58.11448
Figures 55-63 - Male palp of Chedimanops eskovi sp. n. (55–60) and Chedimanops rwenzorensis sp. n. (61–63). 55, 61 dorsal 56, 59 prolateral 57, 60, 62 retrolateral 63 antero-ventral. Abbreviations: Cp claw-shaped process; Em? possible functional embolus; Mp membranous process.
Figures 72-75 from: Zonstein SI, Marusik YM (2017) Descriptions of the two-eyed African spider genera Chedimanops gen. n. and Hybosidella gen. n. (Araneae, Palpimanidae, Chediminae). African Invertebrates 58(1): 23-47. https://doi.org/10.3897/AfrInvertebr.58.11448
Figures 72-75 - Female copulatory organs of Chedimanops rwenzorensis sp. n. 72 epigastral scutum and petiolar sclerites, ventral 73 details of vulval structures, dorsal 74 vulva, focused on grape-shaped glands, dorsal 75 right of vulva, focused on receptacle, dorsal. Abbreviations: Ch receptacular chamber; Fg fine glands; Ft fine threads; Gg grape-shaped glands; Re receptacle.
Figure 5 from: lshishka M, Lazarova S, Radoslavov G, Hristov P, Peneva VK (2017) Biogeography and phylogenetic position of Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. from Maritime Antarctic (Nematoda, Nordiidae). ZooKeys 697: 37-58. https://doi.org/10.3897/zookeys.697.13770
Figure 5 - Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. (= Enchodelus signyensis Loof, 1975). Juveniles (specimens from Livingston Island): A–D Tail ends (J1) E–G Tail ends (J2-J4) Female (specimen from Livingston Island) H Tail end. Scale bar: 50 μm.
Figure 9 from: lshishka M, Lazarova S, Radoslavov G, Hristov P, Peneva VK (2017) Biogeography and phylogenetic position of Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. from Maritime Antarctic (Nematoda, Nordiidae). ZooKeys 697: 37-58. https://doi.org/10.3897/zookeys.697.13770
Figure 9 - Phylogenetic relationships of Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. (= Enchodelus signyensis Loof, 1975) based on 28S rDNA D2-D3 inferred from a Bayesian analysis (GTR+G model) and two Aporcelaimellus species used as an outgroup. * Thonus is currently considered a synonym of Crassolabium (Peña-Santiago & Ciobanu, 2008).
Figure 7 from: lshishka M, Lazarova S, Radoslavov G, Hristov P, Peneva VK (2017) Biogeography and phylogenetic position of Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. from Maritime Antarctic (Nematoda, Nordiidae). ZooKeys 697: 37-58. https://doi.org/10.3897/zookeys.697.13770
Figure 7 - Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. (= Enchodelus signyensis Loof, 1975). Scatter plot of the functional (○) and replacement odontostyle (◊) in relation to the body length of the juvenile stages and females.
Figure 8 from: lshishka M, Lazarova S, Radoslavov G, Hristov P, Peneva VK (2017) Biogeography and phylogenetic position of Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. from Maritime Antarctic (Nematoda, Nordiidae). ZooKeys 697: 37-58. https://doi.org/10.3897/zookeys.697.13770
Figure 8 - Phylogenetic relationships of Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. (= Enchodelus signyensis Loof, 1975) based on 18S rDNA inferred from a Bayesian analysis (GTR+G model) and two Aporcelaimellus species used as an outgroup. * Thonus is currently considered a synonym of Crassolabium (Peña-Santiago and Ciobanu, 2008).
Figure 6 from: lshishka M, Lazarova S, Radoslavov G, Hristov P, Peneva VK (2017) Biogeography and phylogenetic position of Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. from Maritime Antarctic (Nematoda, Nordiidae). ZooKeys 697: 37-58. https://doi.org/10.3897/zookeys.697.13770
Figure 6 - Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. (= Enchodelus signyensis Loof, 1975). Juveniles (specimens from Livingston Island): A–D Anterior ends (J1-J4) F–I Tail ends (J1-J4) Female (specimen from Livingston Island) E Anterior end J Tail end. Scale bar: 10 μm.
Figure 3 from: lshishka M, Lazarova S, Radoslavov G, Hristov P, Peneva VK (2017) Biogeography and phylogenetic position of Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. from Maritime Antarctic (Nematoda, Nordiidae). ZooKeys 697: 37-58. https://doi.org/10.3897/zookeys.697.13770
Figure 3 - SEM micrographs. Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. (= Enchodelus signyensis Loof, 1975). Female: A, D, E Lip region, in face view, amphid aperture B, F Lip region, in sublateral view C Cephalic and labial papillae G–I Vulval region J–L Tail ends. Scale bars: 2 μm (A, C, D, E, F, G); 5 μm (B, I, J); 10 μm (L).
Figure 2 from: lshishka M, Lazarova S, Radoslavov G, Hristov P, Peneva VK (2017) Biogeography and phylogenetic position of Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. from Maritime Antarctic (Nematoda, Nordiidae). ZooKeys 697: 37-58. https://doi.org/10.3897/zookeys.697.13770
Figure 2 - Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. (= Enchodelus signyensis Loof, 1975). Female: A–D Tail ends (A specimen from King George Island; B, C, D specimens from Livingston Island) E–G Tail ends with saccate bodies (E specimen from King George Island F, G specimens from Livingston Island). Scale bar: 10 μm.
Figure 4 from: lshishka M, Lazarova S, Radoslavov G, Hristov P, Peneva VK (2017) Biogeography and phylogenetic position of Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. from Maritime Antarctic (Nematoda, Nordiidae). ZooKeys 697: 37-58. https://doi.org/10.3897/zookeys.697.13770
Figure 4 - Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. (= Enchodelus signyensis Loof, 1975). Juveniles: A–D Anterior ends (J1-J4) (specimens from Livingston Island) Female (specimen from Livingston Island) E Anterior end F Amphideal fovea G Pharyngeal bulb. Enchodelus groenlandicus (Ditlevsen, 1927) H Pharyngeal bulb. Scale bar: 50 μm.
Figure 1 from: lshishka M, Lazarova S, Radoslavov G, Hristov P, Peneva VK (2017) Biogeography and phylogenetic position of Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. from Maritime Antarctic (Nematoda, Nordiidae). ZooKeys 697: 37-58. https://doi.org/10.3897/zookeys.697.13770
Figure 1 - Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. (= Enchodelus signyensis Loof, 1975). Female: A–E Anterior region (A, B specimens from Livingston Island C, D, E specimens from King George Island), black arrows indicate the minute basal swellings F, G Amphideal fovea (E specimen from Livingston Island G specimen from King George Island) H, I Entire body J, K Pharyngeal bulb (J specimen from Livingston Island K specimen from King George Island) L Posterior genital branch (specimen from Livingston Island) M Uterus (specimen from Livingston Island) N–Q Vulval regions (N, O specimens from Livingston Island P, Q specimens from King George Island). Scale bars: 10 μm (A–G, J, K, M–Q); 200 μm (H, I); 20 μm (L).
Figure 9 from: Moreira GRP, Eltz RP, Pase RB, Silva GT, Bordignon SAL, Mey W, Gonçalves GL (2017) Cecidonius pampeanus, gen. et sp. n.: an overlooked and rare, new gall-inducing micromoth associated with Schinus in southern Brazil (Lepidoptera, Cecidosidae). ZooKeys 695: 37-74. https://doi.org/10.3897/zookeys.695.13320
Figure 9 - Natural history of C. pampeanus on S. weinmannifolius. A host plant patch at the type locality; B young developing galls within swollen stems (asterisks); C dissected swollen stem showing developing gall inside (indicated by arrow); D transversally sectioned young gall showing second instar larva inside; E group of external developing galls on branch; F transversally sectioned, full grown gall, showing last instar larva inside; G young dehiscent gall; H detail of emergence orifice left by adult on distal portion of old, empty gall (pointed by arrow in J); I detail of young dehiscent gall (arrow in G), showing orifice clogged by larval feces (asterisk); J old, empty, overwintered gall. Scale bars: 2 mm (B); 1 mm (C, F, G, H, I, J); 0.5 mm (D); 5 mm (E).
Figure 6 from: Moreira GRP, Eltz RP, Pase RB, Silva GT, Bordignon SAL, Mey W, Gonçalves GL (2017) Cecidonius pampeanus, gen. et sp. n.: an overlooked and rare, new gall-inducing micromoth associated with Schinus in southern Brazil (Lepidoptera, Cecidosidae). ZooKeys 695: 37-74. https://doi.org/10.3897/zookeys.695.13320
Figure 6 - Morphology of C. pampeanus first (A, B) and last (C-L) larval instars under scanning electron microscopy. A general aspect, lateral view; B, buccal apparatus, anterior C, head, latero-dorsal D stemmata, lateral; E, left antenna, lateral F maxilla and labium, antero-lateral G labrum and clypeus, latero-dorsal H thorax, latero-ventral I meso- and metathorax in detail, with aligned setae of different lengths, antero-dorsal J second and third abdominal segments, showing tergal calli, latero-dorsal K eight abdominal segment in detail, showing aligned secondary setae (arrows) and spiracle, lateral L last abdominal segments, ventral. Scale bars: 100 µm (A, F, G); 10 µm (B); 200 µm (C); 50 µm (D, E, K); 250 µm (J); 1 mm (H, L); 0.5 mm (I).
Figure 8 from: Moreira GRP, Eltz RP, Pase RB, Silva GT, Bordignon SAL, Mey W, Gonçalves GL (2017) Cecidonius pampeanus, gen. et sp. n.: an overlooked and rare, new gall-inducing micromoth associated with Schinus in southern Brazil (Lepidoptera, Cecidosidae). ZooKeys 695: 37-74. https://doi.org/10.3897/zookeys.695.13320
Figure 8 - Cecidonius pampeanus pupal morphology with scanning electron microscopy. A, B head and prothorax, lateral and dorsal views, respectively C spiracle of sixth abdominal segment, dorsal D subspiracular setae from fourth to sixth abdominal segments, dorsal E tergal spines of eighth abdominal segment, lateral (arrow points to partially closed spiracle) F spines of tenth abdominal segment, posterior-dorsal. Scale bars: 0.5 mm(A); 0.25 mm (B, C, E); 0.1 mm (D, F).
Figure 7 from: Moreira GRP, Eltz RP, Pase RB, Silva GT, Bordignon SAL, Mey W, Gonçalves GL (2017) Cecidonius pampeanus, gen. et sp. n.: an overlooked and rare, new gall-inducing micromoth associated with Schinus in southern Brazil (Lepidoptera, Cecidosidae). ZooKeys 695: 37-74. https://doi.org/10.3897/zookeys.695.13320
Figure 7 - Cecidonius pampeanus pupa with light microscopy, under dorsal (A), ventral (B) and lateral (C) views. Scale bar: 1 mm.
Figure 5 from: Moreira GRP, Eltz RP, Pase RB, Silva GT, Bordignon SAL, Mey W, Gonçalves GL (2017) Cecidonius pampeanus, gen. et sp. n.: an overlooked and rare, new gall-inducing micromoth associated with Schinus in southern Brazil (Lepidoptera, Cecidosidae). ZooKeys 695: 37-74. https://doi.org/10.3897/zookeys.695.13320
Figure 5 - Cecidonius pampeanus last larval instar under light microscopy. A general schematic representation, lateral view B, C head, anterior, and lateral, respectively. Scale bars: 0.5 mm (A); 0.2 mm (B, C).
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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.