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Fig. 11 in Description of immature stages of Laccobius kunashiricus, with a key to genera of the Laccobiini based on larval characters (Coleoptera: Hydrophilidae)
Fig. 11. Mesothoracic leg of Laccobius kunashiricus Shatrovskiy, 1984. First (A) and third (B) instar larva, anterior view.
Fig. 10 in Description of immature stages of Laccobius kunashiricus, with a key to genera of the Laccobiini based on larval characters (Coleoptera: Hydrophilidae)
Fig. 10. Third instar larva of Laccobius kunashiricus Shatrovskiy, 1984, head appendages.A–B – antenna, dorsal (A) and ventral (B) view; C–D – mandible, dorsal view; E–F – maxilla, dorsal (E) and ventral (F) view; G–H – labium, dorsal (G) and ventral (H) view.
Fig. 6 in Description of immature stages of Laccobius kunashiricus, with a key to genera of the Laccobiini based on larval characters (Coleoptera: Hydrophilidae)
Fig. 6. Second instar larva of Laccobius kunashiricus Shatrovskiy, 1984, head appendages. A–B – antenna, dorsal (A) and ventral (B) view; C–D – maxilla, dorsal (C) and ventral (D) view.
Fig. 7 in Description of immature stages of Laccobius kunashiricus, with a key to genera of the Laccobiini based on larval characters (Coleoptera: Hydrophilidae)
Fig. 7. Third instar larva of Laccobius kunashiricus Shatrovskiy, 1984.A – head, dorsal view; B – prosternal sclerite, ventral view; C – mesonotal sclerites, dorsal view; D – spiracular atrium, dorsal view.
Fig. 5 in A new genus and two new species of Leiodinae from Chile, with keys to world genera of Sogdini and Leiodinae from Chile and Argentina (Coleoptera: Leiodidae)
Fig. 5. Habitus and genitalia of Chilean Leiodinae. A–D – Neohydnobius irregularis sp. nov. (A–C – holotype; D – female paratype). E–G –Metahydnobius forticornis (Champion, 1918), male specimen from PN Nahuelbuta. A, E – body in dorsal view; B, F – body in lateral view; C, G –aedeagus in dorsal view; D – spermatheca.
Fig. 3 in A new genus and two new species of Leiodinae from Chile, with keys to world genera of Sogdini and Leiodinae from Chile and Argentina (Coleoptera: Leiodidae)
Fig. 3. Anaballetus chilensis gen. & sp. nov., male paratype.A – meso- and metathorax in ventral view; B – prothorax and anterior leg; C–D – detail of median part of meso- and metaventrite (C – ventral view; D – ventrolateral view); E – protarsus; F – mesothoracic leg; G – mesotarsus; H – metathoracic leg and abdomen. Not to scale.Abbreviations: msvc – mesoventral carina; prre – procoxal rests; trgr – tarsal groove of protibia.
Fig. 2 in A new genus and two new species of Leiodinae from Chile, with keys to world genera of Sogdini and Leiodinae from Chile and Argentina (Coleoptera: Leiodidae)
Fig. 2.Anaballetus chilensis gen. & sp. nov., paratypes (A–D – male; E – female).A – head in ventral view; B – antenna, ventral view; C – detail of mouthparts; D – detail of antennomere 11 in ventral view; E – hind wing. Not to scale.
Fig. 1 in A new genus and two new species of Leiodinae from Chile, with keys to world genera of Sogdini and Leiodinae from Chile and Argentina (Coleoptera: Leiodidae)
Fig. 1. Anaballetus chilensis gen. & sp. nov., holotype (A–D) and female paratype (E–I). A–B – body in dorsal and lateral view; C – head in dorsal view; D – aedeagus in dorsal view; E – mandibles; F – labium; G – maxilla; H – antenna; I – ovipositor in ventral view. Scale bars: 1 mm applies to A–B, 0.25 mm to D–I.
Fig. 7 in A new genus and two new species of Leiodinae from Chile, with keys to world genera of Sogdini and Leiodinae from Chile and Argentina (Coleoptera: Leiodidae)
Fig. 7. Type locality and distribution of Anaballetus chilensis sp. nov. and Neohydnobius irregularis sp. nov. A–B – distribution of both species in Chile; C – flight intercept trap in the Araucaria araucana forest in PN Nahuelbuta (37°49.5′S 73°0.8′W) at which examined specimens were collected; D – general view of the Araucaria forests in the area where specimens were collected (PN Nahuelbuta, view from Piedra de Aguila towards Pehuenco). Photos by M. Fikáček.
Fig. 6. Hydnodiaetus brunneus Jeannel, 1962 in A new genus and two new species of Leiodinae from Chile, with keys to world genera of Sogdini and Leiodinae from Chile and Argentina (Coleoptera: Leiodidae)
Fig. 6. Hydnodiaetus brunneus Jeannel, 1962, male specimen from PN Nahuelbuta.A – body in dorsal view; B – body in lateral view; C – aedeagus in dorsal view.
Figs 146–151 in Taxonomic review of the plant bug genera Amapacylapus and Cylapus with descriptions of two new species and a key to the genera of Cylapini (Hemiptera: Heteroptera: Miridae)
Figs 146–151. Scanning electron micrographs of Cylapus tucuruiensis Carvalho, 1989 (146, 147), Peltidocylapus scutellaris (Poppius, 1909) (148, 149), and Valdasus sp. (150, 151): 146, 149, 151 – thoracic pleura; 147 – pretarsal structure; 148, 150 – lateral view. Abbreviations: ea = evaporative areas; msp = metathoracic spiracle; pc = posterior carina; per = peritreme.
Figs 110–119 in Taxonomic review of the plant bug genera Amapacylapus and Cylapus with descriptions of two new species and a key to the genera of Cylapini (Hemiptera: Heteroptera: Miridae)
Figs 110–119. Male genitalia of Cylapus stellatus (Distant, 1883) (110–114) and C. striatus Reuter, 1907 (115–119): 110, 115 – endosoma; 111, 116 – left paramere (dorsal view); 112, 117 – left paramere (right lateral view); 113, 118 – apical process of left paramere; 114, 119 – right paramere (left lateral view). Abbreviations: bpr = basal process; dss = sclerotized portion of ductus seminis inside endosoma; es1–4 = endosomal sclerites 1–4; pb = paramere body; sg = secondary gonopore; sl = sensory lobe. Scale bars: 0.1 mm.
Figs 97–106 in Taxonomic review of the plant bug genera Amapacylapus and Cylapus with descriptions of two new species and a key to the genera of Cylapini (Hemiptera: Heteroptera: Miridae)
Figs 97–106. Male genitalia of Cylapus marginicollis (Distant, 1883) (97–101) and C. ruficeps Bergroth, 1922 (102–106): 97, 102 – endosoma; 98, 103 – left paramere (dorsal view); 99, 104 – left paramere (right lateral view); 100, 105 – apical process of left paramere; 101, 106 – right paramere (left lateral view). Abbreviations: bpr = basal process; dss = sclerotized portion of ductus seminis inside endosoma; es1–4 = endosomal sclerites 1–4; pb = paramere body; sg = secondary gonopore; sl = sensory lobe. Scale bars: 0.1 mm.
Figs 76–79 in Taxonomic review of the plant bug genera Amapacylapus and Cylapus with descriptions of two new species and a key to the genera of Cylapini (Hemiptera: Heteroptera: Miridae)
Figs 76–79. Scanning electron micrographs of Cylapus antennatus Carvalho & Fontes, 1968 (76–77) and C. citus Bergroth, 1922 (78–79): 76–77 – antennal segment II; 78 – metafemur; 79 – pretarsal structure.
Figs 107–109 in Taxonomic review of the plant bug genera Amapacylapus and Cylapus with descriptions of two new species and a key to the genera of Cylapini (Hemiptera: Heteroptera: Miridae)
Figs 107–109. Scanning electron micrographs of Cylapus striatus Reuter, 1907. 107 – dorsal habitus (♀); 108 – lateral view (♀); 109 – pretarsal structure. Abbreviations: ea = evaporative areas; msp = metathoracic spiracle; pc = posterior carina; per = peritreme.
Figs 56–65 in Taxonomic review of the plant bug genera Amapacylapus and Cylapus with descriptions of two new species and a key to the genera of Cylapini (Hemiptera: Heteroptera: Miridae)
Figs 56–65. Lateral view of Cylapus species: 56 – C. amazonicus Carvalho, 1989 (J); 57 – C. antennatus Carvalho & Fontes, 1968 (J); 58 – C. citus Bergroth, 1922 (♀); 59 – C. luridus sp. nov. (J); 60 – C. marginicollis (Distant, 1883) (J); 61 – C. ruficeps Bergroth, 1922 (♀); 62 – C. stellatus (Distant, 1883) (♀); 63 – C. striatus Reuter, 1907 (♀); 64 – C. tenuicornis (Say, 1832) (J); 65 – C. tucuruiensis Carvalho, 1989 (J).
Figs 36–40 in Taxonomic review of the plant bug genera Amapacylapus and Cylapus with descriptions of two new species and a key to the genera of Cylapini (Hemiptera: Heteroptera: Miridae)
Figs 36–40. Dorsal habitus photographs of Cylapus species: 36 – C. amazonicus Carvalho, 1989 (J); 37–39 – C. antennatus Carvalho & Fontes, 1968 (37 – J holotype, 38 – J, 39 – ♀); 40 – C. citus Bergroth, 1922 (J).
Figs 135–144 in Taxonomic review of the plant bug genera Amapacylapus and Cylapus with descriptions of two new species and a key to the genera of Cylapini (Hemiptera: Heteroptera: Miridae)
Figs 135–144. Male genitalia of Cylapus tenuicornis (Say, 1832) (135–139) and C. tucuruiensis Carvalho, 1989 (140–144): 135, 140 – endosoma; 136, 141 – left paramere (dorsal view); 137, 142 – left paramere (right lateral view); 138, 143 – apical process of left paramere; 139, 144 – right paramere (left lateral view). Abbreviations: bpr = basal process; dss = sclerotized portion of ductus seminis inside endosoma; es1–4 = endosomal sclerites 1–4; pb = paramere body; sg = secondary gonopore; sl = sensory lobe. Scale bars: 0.1 mm.
Figs 66–75 in Taxonomic review of the plant bug genera Amapacylapus and Cylapus with descriptions of two new species and a key to the genera of Cylapini (Hemiptera: Heteroptera: Miridae)
Figs 66–75. Male genitalia of Cylapus amazonicus Carvalho, 1989 (66–70) and Cylapus antennatus Carvalho & Fontes, 1968 (71–75): 66, 71 – endosoma; 67, 72 – left paramere (dorsal view); 68, 73 – left paramere (right lateral view); 69, 74 – apical process of left paramere; 70, 75 – right paramere (left lateral view). Abbreviations: bpr = basal process; dss = sclerotized portion of ductus seminis inside endosoma; es1–4 = endosomal sclerites 1–4; pb = paramere body; sg = secondary gonopore; sl = sensory lobe. Scale bars: 0.1 mm.
Figs 23–26 in Taxonomic review of the plant bug genera Amapacylapus and Cylapus with descriptions of two new species and a key to the genera of Cylapini (Hemiptera: Heteroptera: Miridae)
Figs 23–26. Hemelytron of the species of Amapacylapus Carvalho & Fontes, 1968. 23 – A. amapariensis Carvalho & Fontes, 1968; 24 – A. englemani Carvalho, 1991; 25 – A. labeculosus Bergroth, 1922; 26 – A. unicolor sp. nov. Abbreviations: p1–p7 = yellowish patches; pc = posterior carina; per = peritreme.
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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.