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Figs 1–7. 1 in Wallacea, Pistosia and Neodownesia: three distinct genera and their tribal placement (Coleoptera: Chrysomelidae: Cassidinae)
Figs 1–7. 1 – Neodownesia mediovittata (Gestro, 1920) (Laos: Ban Song Cha, J, 8.7 mm); 2 – N. rubra Gressitt, 1953 (holotype, J, 6.5 mm); 3 – N. sita (Maulik, 1919) (Thailand: Soppong, ♀, 9.0 mm); 4 – Wallacea apicalis Gestro, 1896 (Indonesia: Mentawai Is.: Siberut, 5.3 mm); 5 – Pistosia terminalis (Baly, 1869) (holotype, 9.5 mm, © Natural History Museum, London); 6 – P. maculata (syntype, 12.0 mm, © Museum für Tierkunde, Berlin); 7 – P. testacea (Fabricius, 1801) (Indonesia: Sulawesi: Ahua Creek, 11.1 mm).
Fig. 18 in Description of the larval stages of the berosine genera Berosus and Regimbartia based on the Japanese species B. japonicus and R. attenuata (Coleoptera: Hydrophilidae)
Fig. 18. Living individuals of the hydrophilid larvae.A – Berosus (Berosus) japonicus Sharp, 1873; B – Enochrus (Methydrus) japonicus (Sharp, 1873); C – Laccobius (Laccobius) kunashiricus Shatrovskiy, 1984. Photo A by M. Hayashi, B–C by Y. Minoshima.
Fig. 14 in Description of the larval stages of the berosine genera Berosus and Regimbartia based on the Japanese species B. japonicus and R. attenuata (Coleoptera: Hydrophilidae)
Fig. 14. Third instar larva of Regimbartia attenuata (Fabricius, 1801), head appendages. A–B – antenna, dorsal (A) and ventral (B); C–D – maxilla, dorsal (C) and ventral (D).
Fig. 16 in Description of the larval stages of the berosine genera Berosus and Regimbartia based on the Japanese species B. japonicus and R. attenuata (Coleoptera: Hydrophilidae)
Fig. 16. Regimbartia attenuata (Fabricius, 1801), mesothoracic leg, anterior view. First (A) and third (B) instar.
Fig. 9 in Description of the larval stages of the berosine genera Berosus and Regimbartia based on the Japanese species B. japonicus and R. attenuata (Coleoptera: Hydrophilidae)
Fig. 9. First instar larva of Regimbartia attenuata (Fabricius, 1801), head capsule. A–B – head capsule, dorsal (A) and ventral (B); C – anterior margin of head capsule, dorsal; D–E – variation of sensilla PA15–18, ventral.
Fig. 8 in Description of the larval stages of the berosine genera Berosus and Regimbartia based on the Japanese species B. japonicus and R. attenuata (Coleoptera: Hydrophilidae)
Fig. 8. Third instar larva of Regimbartia attenuata (Fabricius, 1801). A–B – habitus, dorsal (A) and ventral (B); C – cuticular projection on pronotum, dorsal; D – lateral setiferous projection, dorsal; E – cuticular projections on abdominal segment, dorsal.
Fig. 12 in Description of the larval stages of the berosine genera Berosus and Regimbartia based on the Japanese species B. japonicus and R. attenuata (Coleoptera: Hydrophilidae)
Fig. 12. Third instar larva of Regimbartia attenuata (Fabricius, 1801). A – head, dorsal; B – prosternal sclerite, ventral; C – spiracular atrium, dorsal.
Fig. 17. A–B in Description of the larval stages of the berosine genera Berosus and Regimbartia based on the Japanese species B. japonicus and R. attenuata (Coleoptera: Hydrophilidae)
Fig. 17. A–B – Egg-case of Berosus (Berosus) japonicus Sharp, 1873, wild (A) and rearing (B); C – egg-case of Regimbartia attenuata (Fabricius, 1801), rearing; D – egg of R. attenuata. Figs A, C modified after HAYASHI (2009a). Photos by M. Hayashi.
Fig. 4 in Description of the larval stages of the berosine genera Berosus and Regimbartia based on the Japanese species B. japonicus and R. attenuata (Coleoptera: Hydrophilidae)
Fig. 4. First instar larva of Berosus (Berosus) japonicus Sharp, 1873, head appendages. A–B – antenna, dorsal (A) and ventral (B); C–D – left and right mandible, dorsal; E–F – maxilla, dorsal (E) and ventral (F); G–H – labium, dorsal (G) and ventral (H).
Fig. 3 in Description of the larval stages of the berosine genera Berosus and Regimbartia based on the Japanese species B. japonicus and R. attenuata (Coleoptera: Hydrophilidae)
Fig. 3. First instar larva of Berosus (Berosus) japonicus Sharp, 1873, anterior margin of head capsule, dorsal (A) and ventral (B) (both drawn from dorsal).
Fig. 10 in Description of the larval stages of the berosine genera Berosus and Regimbartia based on the Japanese species B. japonicus and R. attenuata (Coleoptera: Hydrophilidae)
Fig. 10. First instar larva of Regimbartia attenuata (Fabricius, 1801), head appendages. A–B – antenna, dorsal (A) and ventral (B); C–D – maxilla, dorsal (C) and ventral (D).
Figs 7–9 in Two new genera of Keroplatidae (Diptera), with an updated key to the World genera of Keroplatini
Figs 7–9. Asiokeroplatus tiger gen. & sp. nov., holotype. 7 – male terminalia, dorsal view; 8 – terminalia, ventral view; 9 – terminalia and abdominal segments VII and VIII, ventral view.
Figs 1–2 in Two new genera of Keroplatidae (Diptera), with an updated key to the World genera of Keroplatini
Figs 1–2. Afrokeroplatus ashleyi gen. & sp. nov. 1 – male habitus (scale bar 1 mm); 2 – male head, frontal view.
Figs 4–5 in Two new genera of Keroplatidae (Diptera), with an updated key to the World genera of Keroplatini
Figs 4–5. Afrokeroplatus ashleyi gen. & sp. nov., male terminalia. 4 – dorsal view; 5 – ventral view.
Figs. 5–9 in Two new genera of the family Scathophagidae (Diptera)
Figs. 5–9. Suwaia longicornis (Hendel, 1913). 5–8 – J paratype: 5 – abdominal sternites 4 to 5; 6 – cerci and surstyli (caudal view); 7 – pregonite and postgonite (lateral view); 8 – epiphallus, pregonites, postgonites and lateral membraneous lobes (dorsal view). 9 – ♀ paratype, abdominal stenites 6 to 8 (lateral view). Scale bars: 0.5 mm (Figs. 5–6, 9), 0.1 mm (Figs. 7–8).
Figs. 1–4 in Two new genera of the family Scathophagidae (Diptera)
Figs. 1–4. Jezekia kmenti sp. nov. 1–3 – J paratype: 1 – abdominal sternites 3 to 5; 2 – cerci and surstyli; 3 – pregonites and epiphallus. 4 – ♀ paratype, abdominal sternites 5 to 8. Scale bars: 0.5 mm (Figs. 1–2, 4), 0.1 mm (Fig. 3).
Figs 69–71 in Two new genera of Madagascan Pentatominae (Hemiptera: Heteroptera: Pentatomidae)
Figs 69–71. Nene elongatum sp. nov. 69–70 – external female genitalia (69 – intact, 70 – dissected). 71 – spermatheca. Triangulin not depicted. Abbreviations: ar – apical receptacle of spermatheca, dd – distal duct of spermatheca, df – distal flange, dil – spermathecal dilation, div – distal invagination of spermathecal duct, ip – intermediate part of spermatheca, lt8,9 – laterotergite VIII and IX, pd – proximal duct of spermatheca, pf – proximal flange, sp – spiracle, rs – ring sclerite, so – sclerite surrounding spermathecal opening, vf8,9 – valvifer VIII and IX, X – segment X. Scale bars: 1 mm.
Fig. 9 in Description of immature stages of Laccobius kunashiricus, with a key to genera of the Laccobiini based on larval characters (Coleoptera: Hydrophilidae)
Fig. 9. Third instar larva of Laccobius kunashiricus Shatrovskiy, 1984, anterior margin of head capsule, dorsal (A) and ventral (B) (both drawn from dorsal).
Fig. 8 in Description of immature stages of Laccobius kunashiricus, with a key to genera of the Laccobiini based on larval characters (Coleoptera: Hydrophilidae)
Fig. 8. Third instar larva of Laccobius kunashiricus Shatrovskiy, 1984, head capsule, dorsal (A) and ventral (B) view.
Fig. 4 in Description of immature stages of Laccobius kunashiricus, with a key to genera of the Laccobiini based on larval characters (Coleoptera: Hydrophilidae)
Fig. 4. First instar larva of Laccobius kunashiricus Shatrovskiy, 1984, anterior margin of head capsule, dorsal (A) and ventral (B) view (both views drawn from a slide with the head capsule mounted with dorsal side up).
ScienceDex guides
Understand access before you commit
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.