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450 results for “external morphology”
Figs. 11–16 in The external morphology of eggs of three Rhopalidae species (Hemiptera: Heteroptera) with a review of the eggs of this family
Figs. 11–16. Eggs of Brachycarenus tigrinus (Schilling, 1829). 11 – empty egg with separated pseudoperculum, ventral view; 12 – empty egg with separated pseudoperculum, lateral view; 13 – detail of boundary-line between egg body and pseudoperculum, anterolateral view; 14 – detail of micropylar process, most exposed view; 15 – anterior pole of egg with one micropylar process visible, dorsal view; 16 – detail of chorion pattern with rounded elevated tubercles. Scale = 100 μm for Figs. 11, 12, 15; 50 μm for Fig. 13; 10 μm for Figs 14, 16. Letterings: m1, m2 – micropylar processes; p – pseudoperculum.
Figs. 1–8 in The external morphology of eggs of three Rhopalidae species (Hemiptera: Heteroptera) with a review of the eggs of this family
Figs. 1–8. Eggs of Chorosoma schillingi (Schilling, 1829). 1 – whole egg, ventral view; 2 – whole egg, lateral view; 3 – anterior pole of egg, lateral view; 4 – anterior pole of egg, ventral view; 5 – empty egg with separated pseudoperculum, ventral view; 6 – detail of chorion surface pattern, pseudoperculum; 7 – detail of chorion surface pattern, egg body; 8 – detail of adhesive stalk on dorsal side, lateral view. Scale = 100 μm for Figs. 1–5; 10 μm for Figs. 6–8. Letterings: c – cap; m1, m2 – micropylar processes; p – pseudoperculum; r – ridge separating pseudoperculum from surrounding chorion; s – attachment stalk.
Fig. 11 in NGS-barcodes, haplotype networks combined to external morphology help to identify new species in the mangrove genus Ngirhaphium Evenhuis & Grootaert, 2002 (Diptera: Dolichopodidae: Rhaphiinae) in Southeast Asia
Fig. 11. Haplotype network of Ngirhaphium sivasothii. Thailand: Krabi, Phangnga, Satun; Singapore: Sarimbun, Pulau Tekong, Pulau Ubin, Labrador, Semakau Island, and Sungei Buloh.
Fig. 10 in NGS-barcodes, haplotype networks combined to external morphology help to identify new species in the mangrove genus Ngirhaphium Evenhuis & Grootaert, 2002 (Diptera: Dolichopodidae: Rhaphiinae) in Southeast Asia
Fig. 10. Haplotype network of Ngirhaphium murphyi. Singapore: Pulau Ubin, Mandai Sungei Buloh; Thailand: Satun and Krabi.
Fig. 12 in NGS-barcodes, haplotype networks combined to external morphology help to identify new species in the mangrove genus Ngirhaphium Evenhuis & Grootaert, 2002 (Diptera: Dolichopodidae: Rhaphiinae) in Southeast Asia
Fig. 12. Compilation of male terminalia of Ngirhaphium in lateral view. A, Ngirhaphium sivasothii left side with ventral surstylus removed; cerci dorsally; B, Ngirhaphium murphyi left side with ventral surstylus removed; cerci and dorsal surstyli dorsally; C, Ngirhaphium caeruleum left side with ventral surstylus removed; cerci and dorsal surstyli dorsally; D, Ngirhaphium meieri, new species left side with ventral surstylus removed; E, Ngirhaphium chutamasae left side with ventral surstylus removed; F, Ngirhaphium thaicum, new species right side. Scale = 0.1 mm.
Fig. 8 in NGS-barcodes, haplotype networks combined to external morphology help to identify new species in the mangrove genus Ngirhaphium Evenhuis & Grootaert, 2002 (Diptera: Dolichopodidae: Rhaphiinae) in Southeast Asia
Fig. 8. Ngirhaphium meieri, new species, holotype male terminalia: A, Lateral view of genital capsule with left ventral surstylus removed; B, Cerci dorsally; C. Left ventral surstylus; D, Ventral view of genital capsule. Abbreviations: ae = aedeagus; c = cercus; ds = dorsal surstylus; hy = hypandrium; sp = sperm pump; vs = ventral surstylus. Scale = 0.1 mm.
Fig. 5 in NGS-barcodes, haplotype networks combined to external morphology help to identify new species in the mangrove genus Ngirhaphium Evenhuis & Grootaert, 2002 (Diptera: Dolichopodidae: Rhaphiinae) in Southeast Asia
Fig. 5. Ngirhaphium thaicum, new species male terminalia (27_009) A, epandrium left side; B, cerci dorsal view; C, left surstylus inside view. Scale = 0.1 mm.
Fig. 2 in NGS-barcodes, haplotype networks combined to external morphology help to identify new species in the mangrove genus Ngirhaphium Evenhuis & Grootaert, 2002 (Diptera: Dolichopodidae: Rhaphiinae) in Southeast Asia
Fig. 2. Ngirhaphium caeruleum-complex. View of inside of the dorsal surstylus of the left side and the fused dorsal and ventral surstyli of the right side. Scale = 0.1mm. A, green caeruleum from Tutong, Brunei (ZRCBDP0066395) at 1.6 % from the Semakau population; B, green caeruleum from Pulau Tekong, Singapore (ZRCBDP0001462) at 0.6% from the Semakau population; C, green caeruleum from Pulau Ubin, Singapore (ZRC_BDP_0084430) at 0.6% from the Semakau population; D, blue caeruleum from the type locality on Semakau Island, Singapore (ZRCBDP0118762); E, green thaicum, new species from Surat Thani, Thailand (24-018) at 4.2% from the Semakau population; F, green thaicum, new species from Cambodia (JP3C_Ngi-cambodiensis_Misc002) within the variability of the southern Thailand populations.
Fig. 1 in NGS-barcodes, haplotype networks combined to external morphology help to identify new species in the mangrove genus Ngirhaphium Evenhuis & Grootaert, 2002 (Diptera: Dolichopodidae: Rhaphiinae) in Southeast Asia
Fig. 1. Haplotype network of the Ngirhaphium caeruleum-complex. Brunei: Berambang, Tutong, Labu; Singapore: Pulau Ubin, Pulau Tekong, Semakau Island; Thailand: Chumphon, Surat Thani, and Cambodia.
Fig. 8 in Scanning the Hyocephalidae: details of their external morphology with respect to phylogenetic relationships within Eutrichophora (Hemiptera: Heteroptera)*
Fig. 8. Abdominal trichobothria in Hyocephalus aprugnus Bergroth, 1906, female: A – position of trichobothria on sternites III and IV (AT3 and AT4) (magnification 45×); B – AT3 (300×); C–D – AT4 (C – 400×, D – 800×); E–G – AT5 (E – 160×, F – 300×, G – 800×); H – AT6 (300×). Abbreviations: AT3–4 – abdominal trichobothria on sternites III to IV; bo – bothrium; cs – crocus-like structure; sp – spiracle; tr – trichome. Scale bars: 50 μm (D, G), 0.1 mm (B–C, F, H), 0.3 mm (E), 1 mm (A).
Fig. 5 in Scanning the Hyocephalidae: details of their external morphology with respect to phylogenetic relationships within Eutrichophora (Hemiptera: Heteroptera)*
Fig. 5. External scent efferent system of dorsoabdominal glands in Hyocephalidae. A–F – Hyocephalus aprugnus Bergroth, 1906, female: A – abdomen, dorsal view (magnification 19×); B, D, E – dorsoabdominal scent efferent system on tergites IV–V (B – 47×, D – 200×, E – 400×); C, F – dorsoabdominal scent efferent system on tergites V–VI (C – 80×, F – 200×). G–K – Maevius luridus Brailovsky, 2002, male: abdomen, dorsal view (30×); H – suture between tergites III and IV (42×); I, K – dorsoabdominal scent efferent system on tergites IV–V (I – 130×, K – 500×); J – dorsoabdominal scent efferent system on tergites V–VI (120×). Abbreviations: DAGIV–V, DAGV–VI – scent efferent system of dorsoabdominal scent glands on tergites IV–V and V–VI, respectively. Scale bars: 0.1 mm (E, K), 0.2 mm (D, F), 0.4 mm (I–J), 0.5 mm (C), 1 mm (B, G–H), 3 mm (A).
Fig. 4 in Scanning the Hyocephalidae: details of their external morphology with respect to phylogenetic relationships within Eutrichophora (Hemiptera: Heteroptera)*
Fig. 4. Ultrastructure of thoracic spiracles in Hyocephalidae. A–C – Hyocephalus aprugnus Bergroth, 1906, male: A – mesothoracic spiracle (magnifi- cation 400×); B–C – metathoracic spiracle (B – 200×, C – 500×). D – Maevius luridus Brailovsky, 2002: metathoracic spiracle (500×). Scale bars: 0.1 mm (A, C–D), 0.2 mm (B).
Fig. 2 in Scanning the Hyocephalidae: details of their external morphology with respect to phylogenetic relationships within Eutrichophora (Hemiptera: Heteroptera)*
Fig. 2. Head and prothorax of Hyocephalidae. A–C – Maevius luridus Brailovsky, 2002, male: A – dorsal habitus (magnification 13×); B – head and pronotum, dorsal view (32×), C – apex of profemur with spines (130×). D–H – Hyocephalus aprugnus Bergroth, 1906, female: D–F – head and prothorax (D – dorsal view, 23×; E – lateral view, 21×; F – ventral view, 23×); G–H – head (G – dorsal view, 40×; H – lateral view, 30×). Scale bars: 0.4 mm (C), 1 mm (B, G–H), 2 mm (D–F), 4 mm (A).
Fig. 1 in Scanning the Hyocephalidae: details of their external morphology with respect to phylogenetic relationships within Eutrichophora (Hemiptera: Heteroptera)*
Fig. 1. Dorsal habitus of Hyocephalidae. A – Hyocephalus aprugnus Bergroth, 1906, female (15.4 mm); B – Maevius luridus Brailovsky, 2002, male (8.7 mm).
Fig. 7 in Scanning the Hyocephalidae: details of their external morphology with respect to phylogenetic relationships within Eutrichophora (Hemiptera: Heteroptera)*
Fig. 7. Schematic drawing of abdomen of Maevius luridus Brailovsky, 2002, male, in lateral view. Scale bar: 1 mm.Abbreviations: AT3–7a–c – particular positions of abdominal trichobothria on sternites III–VII; sml – submarginal depressed line; sp – spiracle; tss – tergosternal suture.
Fig. 3 in Scanning the Hyocephalidae: details of their external morphology with respect to phylogenetic relationships within Eutrichophora (Hemiptera: Heteroptera)*
Fig. 3. External scent efferent system of metathoracic glands in Hyocephalidae. A–E – Hyocephalus aprugnus Bergroth, 1906 (A–D – male, E – female): A – meso- and metathorax, lateral view (magnification 37×); B – external scent efferent system, lateral view (60×); C – ostiole and peritreme, lateral view (180×); D – peritreme, lateral view (300×); E – ostiole and peritreme, ventral view (180×). F–H – Maevius luridus Brailovsky, 2002: F – external scent efferent system, lateral view (85×); G – ostiole and peritreme, lateral view (250×); H – peritreme, lateral view (550×).Abbreviations: mss – mesothoracic spiracle, mts – metathoracic spiracle, o – ostiole, vs – vestibular scar. Scale bars: 0.1 mm (D, H), 0.2 mm (G), 0.3 mm (C, E), 0.5 mm (B, F), 1 mm (A).
Fig. 6 in Scanning the Hyocephalidae: details of their external morphology with respect to phylogenetic relationships within Eutrichophora (Hemiptera: Heteroptera)*
Fig. 6. Strainer organ in Hyocephalidae. A–D – Hyocephalus aprugnus Bergroth, 1906: A – female, abdomen, lateral view (magnification 18×); B–D – strainer (B – male, 150×; C – female, 150×; D – female, 600×). E – Maevius luridus Brailovsky, 2002, male, strainer (370×). F – Maevius indecorus (Stål, 1874), female, strainer (250×).Abbreviations:AT3–7 – abdominal trichobothria on sternites III–VII; cp – closed pore; op – open pore; st – strainer. Scale bars: 50 μm (D), 0.1 mm (E), 0.2 mm (F), 0.3 mm (B–C), 3 mm (A).
Fig. 9 in Scanning the Hyocephalidae: details of their external morphology with respect to phylogenetic relationships within Eutrichophora (Hemiptera: Heteroptera)*
Fig. 9. Details of abdomen and thorax in Hyocephalidae and Stenocephalidae. A–B – Hyocephalus aprugnus Bergroth, 1906, female: A – abdominal trichobothria on sternite VI (AT6) (magnification 800×); B – AT7 (400×). C–D – Maevius luridus Brailovsky, 2002, male: C – AT5 (400×), D – AT6 (400×). E–H – Dicranocephalus agilis (Scopoli, 1763): E – external scent efferent system (261×); F – abdomen in lateral view (27×); G–H – abdominal trichobothria on sternite VI (G – 120×, H – 400×). Abbreviations: AT5–7 – abdominal trichobothria 5–7; bo – bothrium; o – ostiole; pe – peritreme; sp – spiracle. Scale bars: 50 μm (A), 0.1 mm (B–D).
Fig. 14 in Larval external morphology and development in Feihyla kajau (Dring, 1983) (Amphibia: Anura: Rhacophoridae)
Fig. 14. Mean number of days in each developmental stage (between Stages 26 and 41) in Feihyla kajau.
Fig. 12 in Larval external morphology and development in Feihyla kajau (Dring, 1983) (Amphibia: Anura: Rhacophoridae)
Fig. 12. Morphological changes of Feihyla kajau tadpole at Stage 42 in lateral (top) and dorsal (bottom) views.
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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)
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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.