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Fig. 1 in Comparison of two traps for monitoring California red scale (Hemiptera: Diaspididae)
Fig. 1. The California red scale traps used in this study deployed in the field. (A) Single-sided California red scale trap, consisting of a wirelessly networked digital camera mounted to a sticky card platform. (B) A commercial double-sided California red scale trap.
Fig. 3 in Comparison of two traps for monitoring California red scale (Hemiptera: Diaspididae)
Fig. 3. (A) Mean (± SE) California red scale counts (based on estimated California red scale counts) for all trap locations in this study. (B) Schematic of relative position of trap locations in our field plot; shape indicates estimated marginal mean California red scale counts. In (A) and (B) circles are <500 California red scale, triangle is 501 to 1,000 California red scale, and squares> 1,000 California red scale. (C) Mean (± SE) California red scale trap counts by flight number. Bars with different letters are significantly different (α = 0.05).
Fig. 4 in Comparison of two traps for monitoring California red scale (Hemiptera: Diaspididae)
Fig. 4. The probability of a trap capturing> 1,000 California red scale in a sampling period, based on (A) actual California red scale counts, and (B) estimated California red scale counts. Male flight periods are delimited with vertical dashed lines.
Fig. 1 in Ophiotaenia echidis n. sp. (Cestoda: Proteocephalidae) from the saw-scaled viper, Echis carinatus sochureki Stemmler (Ophidia: Viperidae), one of the world's deadliest snakes, from the United Arab Emirates
Fig. 1. Scanning electron micrographs of Ophiotaenia echidis n. sp. from Echis carinatus sochureki, United Arab Emirates. A – subapical view of the scolex. B – frontal view of the scolex. C – detail of suckers. D–J – microtriches on the apex of the scolex, external (non-adherent) surface of suckers, upper rim, luminal surface and lower rim of suckers, between suckers and neck, respectively. Note: small black letters in A and B correspond to the figures showing higher magnification images of these surfaces.
Fig. 3. Ophiotaenia echidis n in Ophiotaenia echidis n. sp. (Cestoda: Proteocephalidae) from the saw-scaled viper, Echis carinatus sochureki Stemmler (Ophidia: Viperidae), one of the world's deadliest snakes, from the United Arab Emirates
Fig. 3. Ophiotaenia echidis n. sp. from Echis carinatus sochureki, United Arab Emirates. A - pregravid proglottid, holotype, MHNG-PLAT-0137383, dorsal view. B – gravid proglottid, paratype, IPCAS C-876/1, ventral view. Abbrevations: cs: cirrus-sac; eci: everted cirrus; oc: osmoregulatory canal; ov: ovary; te: testes; ut: uterus; vc: vaginal canal; vf: vitelline follicles.
Fig. 2. Ophiotaenia echidis n in Ophiotaenia echidis n. sp. (Cestoda: Proteocephalidae) from the saw-scaled viper, Echis carinatus sochureki Stemmler (Ophidia: Viperidae), one of the world's deadliest snakes, from the United Arab Emirates
Fig. 2. Ophiotaenia echidis n. sp. from Echis carinatus sochureki, United Arab Emirates. A – scolex, IPCAS C-876/1 (UAE 04). B – posterior part of proglottid, holotype, MHNG-PLAT-0137383, dorsal view. C – terminal genitalia with evaginated cirrus and vaginal sphincter, MHNG-PLAT-0137385, ventral view. D – cross section at level of anterior part of pregravid proglottid, MHNG-PLAT-0120507. E – egg with a trilayered embryophore, drawn in distilled water, MHNG-PLAT-0120507. F – cross section at level of the vagina, showing the vaginal sphincter, mature proglottid, MHNG-PLAT-0120507. G – terminal genitalia, C-876/1 (UAE 04 TS), dorsal view. H, I – eggs with a trilayered embryophore, drawn in distilled water, MHNG-PLAT-0120507. Abbrevations: ci: cirrus; cs: cirrus-sac; doc: dorsal osmoregulatory canal; ec: ejaculatory duct; em: trilayered embryophore; ilm: internal longitudinal musculature; ln: longitudinal nerve cord; loc: lateral osmoregulatory canal; Mg: Mehlis' glands; oc: secondary osmoregulatory canals; oe: outer envelope; on: oncosphere; ot: ootype; ov: ovary; sc: subtegumental cells; te: testes; tg: tegument; ud: uterine diverticula; up: uterine pore; us: uterine stem; ut: uterus; va: vas deferens; vc: vaginal canal; vd: vitelline duct; vf: vitelline follicles; voc: ventral osmoregulatory canal; vs: vaginal sphincter.
Fig. 4 in Ophiotaenia echidis n. sp. (Cestoda: Proteocephalidae) from the saw-scaled viper, Echis carinatus sochureki Stemmler (Ophidia: Viperidae), one of the world's deadliest snakes, from the United Arab Emirates
Fig. 4. Maximum likelihood phylograms of the relationships of Ophiotaenia echidis n. sp. among selected Proteocephalidae inferred from partial lsrDNA (A), and concatenated lsrDNA + COI datasets (B). Colours of branch and species names correspond to the zoogeographical realms of the isolates as proposed by Holt et al. (2013) (see inset). Branch length scale bar indicates number of substitutions per site. Abbreviations: AUS, Australian; AFR, Afrotropical; MAD, Madagascan; NEA, Nearctic; NEO, Neotropical; PAN, Panamanian; ORI, Oriental; SAH, Saharo-Arabian; * indicates tapeworms from viperid snakes (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 1 in Effects of small-scale anthropogenic alterations in Euglossini bees at eastern Amazon forest
Fig. 1. Sampling transects located in the Caxiuanà National Forest, northeastern of ParÁ State, Brazil.
Fig. 3 in Anuran assemblage changes along small-scale phytophysiognomies in natural Brazilian grasslands
Fig. 3. Anuran species found in two phytophysiognomy types of EstaÇão Ecológica do Taim, southern Brazil, between May 2011 and April 2012. The pink, green and mixed circles (green and pink) indicate the species that were recorded, respectively, in grassland areas, forest areas, and in both areas. (a) Elachistocleis bicolor (GuÉrin-MÉneville, 1838); (b) Boana pulchella (DumÉril & Bibron, 1841); (c) Leptodactylus gracilis (DumÉril & Bibron, 1840); (d) Leptodactylus latinasus (JimÉnez de la Espada, 1875); (e) Leptodactylus luctator (Hudson, 1892); (f) Odontophrynus maisuma (Reinhardt & LÜtken, 1862); (g) Physalaemus biligonigerus (Cope, 1861); (h) Physalaemus gracilis (Boulenger, 1883); (i) Pseudis minuta (GÜnther, 1858); (j) Pseudopaludicola falcipes (Hensel, 1867); (k) Rhinella dorbignyi (DumÉril & Bibron, 1841); (l) Scinax granulatus (Peters, 1871); (m) Scinax squalirostris (Lutz, 1925).
Fig. 2 in Anuran assemblage changes along small-scale phytophysiognomies in natural Brazilian grasslands
Fig. 2. Phytophysiognomies of ESEC Taim, Rio Grande do Sul, Brazil: (A) sites of grassland dominance and (B) sites of forest dominance.
Fig. 2 in Effects of small-scale anthropogenic alterations in Euglossini bees at eastern Amazon forest
Fig. 2. Abundances of individuals (A), species richness (B) and species diversity (C) of the Euglossine bees between areas (altered and preserved) in the Caxiuanà National Forest, ParÁ, Brazil.
Fig. 1 in Anuran assemblage changes along small-scale phytophysiognomies in natural Brazilian grasslands
Fig. 1. Geographic location of the study site (C) on the EstaÇão Ecológica do Taim (B) in the state of Rio Grande do Sul (A), Brazil.
Fig. 3 in Effects of small-scale anthropogenic alterations in Euglossini bees at eastern Amazon forest
Fig. 3. PCoA ordination showing differences in species composition of Euglossini bees sampled in transects of the preserved area (triangles) and transects of the altered area (circles) at Caixuanà National Forest, ParÁ, Brazil.
Fig. 2 in The importance of considering small-scale variability in macrobenthic distribution: spatial segregation between two fiddler crab species (genus Leptuca) (Decapoda, Ocypodidae)
Fig. 2. NMDS ordination (stress = 0.16) of sites based on similarity of group composition. Leptuca leptodactyla (Rathbun in Rankin, 1898): JLM (juvenile males), JLF (juvenile females), ALM (adult males) and ALF (adult females). Leptuca uruguayensis (Nobili, 1901): JUM (juvenile males), JUF (juvenile females), AUM (adult males) and AUF (adult females).
Fig. 1 in The importance of considering small-scale variability in macrobenthic distribution: spatial segregation between two fiddler crab species (genus Leptuca) (Decapoda, Ocypodidae)
Fig. 1. Schematic representation of the sampling design, with subarea separation and the six random replicates. (Area=10 m²).
Fig. 4 in An ankylosaurid dinosaur from Mongolia with in situ armour and keratinous scale impressions
Fig. 4. Tail of an ankylosaurid dinosaur Tarchia cf. gigantea, ZPAL MgD I/113 from the Nemegt Formation at Altan Uul III, Mongolia, compared to tail of Saichania (MPC 100/1305) from the Baruungoyot Formation at Khulsan, Mongolia. Osteoderms found attached to the tail of ZPAL MgD I/113 are marked by numbers according to the Types 1–10 description in the text.
Fig. 3 in An ankylosaurid dinosaur from Mongolia with in situ armour and keratinous scale impressions
Fig. 3. An ankylosaurid dinosaur Tarchia cf. gigantea, ZPAL MgD I/113 from the Nemegt Formation at Altan Uul III, Mongolia. A. Dorsal view of the trunk. Skin impressions and osteoderms are visible on the trunk. Osteoderms are positioned in situ along the vertebral column. The specimen only represents the posterior part of the trunk. B. Interpretive drawing of osteoderms (white) and scale imprints (grey).
Fig. 5 in An ankylosaurid dinosaur from Mongolia with in situ armour and keratinous scale impressions
Fig. 5. Dorsal view of the most distal part of the tail preserved in an ankylosaurid dinosaur Tarchia cf. gigantea, ZPAL MgD I/113 from the Nemegt Formation at Altan Uul III, Mongolia. Five relatively small scutes cover the vertebrae (Types 6 and 8). Two large plates fuse to the centra of the three most distal vertebrae. Note the large grooves on both plates (darkened and arrowed), and the shapes of the distal keels. One handle vertebra is darkened to show the interlocking prezygapophyses and neural spines. Anterior is to the right.
Рис. 87–96. КопуΛятивные органы виΑов роΑа Zelotes. 87–88, 90–91, 93–94 – Z. gallicus; 89, 92, 95–96 – Z. pseudogallicus. 87–92 – паΛьпа самца вентраΛьно; 93–96 – эпигина: 93, 95 – вентраΛьно, 94, 96 – ΑорсаΛьно. ЭкземпΛяры: 87, 90 – из Αагонаки, АΑыгея; 88, 91, 93–94 – из Верхнего Зарамага, Северная Осетия; 89, 92, 95–96 – из Ростовской обΛасти. Масштабные Λинейки 0.25 мм. Figs 87–96. Copulatory organs of Zelotes spp. 87–88, 90–91, 93–94 – Z. gallicus; 89, 92, 95–96 – Z. pseudogallicus; 87–92 – male palp, ventral view; 93–96 – epigyne: 93, 95 – ventral view, 94, 96 – dorsal view. Specimens: 87, 90 – from Lagonaki, Adygea; 88, 91, 93–94 – from Verkhniy Zaramag, North Ossetia; 89, 92, 95–96 – from Rostov Region. Scale bars 0.25 mm. in A review of spiders of the genus Zelotes Gistel, 1848 of the subterraneus-group (Aranei: Gnaphosidae) from the Caucasus and Ciscaucasia
Рис. 87–96. КопуΛятивные органы виΑов роΑа Zelotes. 87–88, 90–91, 93–94 – Z. gallicus; 89, 92, 95–96 – Z. pseudogallicus. 87–92 – паΛьпа самца вентраΛьно; 93–96 – эпигина: 93, 95 – вентраΛьно, 94, 96 – ΑорсаΛьно. ЭкземпΛяры: 87, 90 – из Αагонаки, АΑыгея; 88, 91, 93–94 – из Верхнего Зарамага, Северная Осетия; 89, 92, 95–96 – из Ростовской обΛасти. Масштабные Λинейки 0.25 мм. Figs 87–96. Copulatory organs of Zelotes spp. 87–88, 90–91, 93–94 – Z. gallicus; 89, 92, 95–96 – Z. pseudogallicus; 87–92 – male palp, ventral view; 93–96 – epigyne: 93, 95 – ventral view, 94, 96 – dorsal view. Specimens: 87, 90 – from Lagonaki, Adygea; 88, 91, 93–94 – from Verkhniy Zaramag, North Ossetia; 89, 92, 95–96 – from Rostov Region. Scale bars 0.25 mm.
Рис. 80–86. КопуΛятивные органы Zelotes dagestanus Ponomarev, sp. n. 80–83 – паΛьпа самца: 80–82 – вентраΛьно, 83 – ΛатераΛьно; 84 – буΛьбус ΛатераΛьно; 85–86 – эпигина: 85 – вентраΛьно, 86 – ΑорсаΛьно. 80, 82–86 – экземпΛяры с бархана Сарыкум, Δагестан; 81 – экземпΛяр из окрестностей с. Гаша, Δагестан. Масштабная Λинейка 0.25 мм. Figs 80–86. Copulatory organs of Zelotes dagestanus Ponomarev, sp. n. 80–83 – male palp: 80–82 – ventral view, 83 – lateral view; 84 – bulbus, lateral view; 85–86 – epigyne: 85 – ventral view, 86 – dorsal view. 80, 82–86 – specimens from barkhan Sarykum, Dagestan; 81 – specimen from Gasha village environs, Dagestan. Scale bar 0.25 mm. in A review of spiders of the genus Zelotes Gistel, 1848 of the subterraneus-group (Aranei: Gnaphosidae) from the Caucasus and Ciscaucasia
Рис. 80–86. КопуΛятивные органы Zelotes dagestanus Ponomarev, sp. n. 80–83 – паΛьпа самца: 80–82 – вентраΛьно, 83 – ΛатераΛьно; 84 – буΛьбус ΛатераΛьно; 85–86 – эпигина: 85 – вентраΛьно, 86 – ΑорсаΛьно. 80, 82–86 – экземпΛяры с бархана Сарыкум, Δагестан; 81 – экземпΛяр из окрестностей с. Гаша, Δагестан. Масштабная Λинейка 0.25 мм. Figs 80–86. Copulatory organs of Zelotes dagestanus Ponomarev, sp. n. 80–83 – male palp: 80–82 – ventral view, 83 – lateral view; 84 – bulbus, lateral view; 85–86 – epigyne: 85 – ventral view, 86 – dorsal view. 80, 82–86 – specimens from barkhan Sarykum, Dagestan; 81 – specimen from Gasha village environs, Dagestan. Scale bar 0.25 mm.
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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.