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FIGURE 3 in Eriophyes species (Acari: Eriophyoidea) inhabiting lime trees (Tilia spp.: Tiliaceae) — supplementary description and morphological variability related to host plants and female forms
FIGURE 3. Eriophyes exilis (Nalepa 1892). Deutogyne female. D. Dorsal view; SA. Lateral view of anterior region; CG. Coxigenital region; IG. Internal genitalia; L1. Leg I; L2. Leg II; em. Empodium (enlarged). Scale bar: 50 µm for D, CG, IG & SA; 25 µm for L1 & L2.
FIGURE 19 in Eriophyes species (Acari: Eriophyoidea) inhabiting lime trees (Tilia spp.: Tiliaceae) — supplementary description and morphological variability related to host plants and female forms
FIGURE 19. Digital micrographs of Eriophyes tiliae Nalepa 1890. Nymph. A. Dorsal view of anterior region; B. Ventral view of anterior region. Scale bar: 10 µm for A & B.
FIGURE 14 in Eriophyes species (Acari: Eriophyoidea) inhabiting lime trees (Tilia spp.: Tiliaceae) — supplementary description and morphological variability related to host plants and female forms
FIGURE 14. Digital micrographs of Eriophyes nervalis (Nalepa 1918). Nymph. A. Dorsal view of anterior region; B. Ventral view of anterior region. Scale bar: 10 µm for A & B.
FIGURE 6 in Eriophyes species (Acari: Eriophyoidea) inhabiting lime trees (Tilia spp.: Tiliaceae) — supplementary description and morphological variability related to host plants and female forms
FIGURE 6. Vein angle galls on leaf of Tilia platyphyllos inhabited by Eriophyes exilis (Nalepa 1892) and Eriophyes nervalis (Nalepa 1918).
FIGURE 15. Eriophyes tiliae Nalepa 1890. Protogyne female. D in Eriophyes species (Acari: Eriophyoidea) inhabiting lime trees (Tilia spp.: Tiliaceae) — supplementary description and morphological variability related to host plants and female forms
FIGURE 15. Eriophyes tiliae Nalepa 1890. Protogyne female. D. Dorsal view; SA. Lateral view of anterior region; CG. Coxigenital region; IG. Internal genitalia; L1. Leg I; L2. Leg II. em. Empodium (enlarged). Male. E. Epiandrium. Scale bar: 50 µm for D, SA, CG, E & IG; 25 µm for L1 & L2.
FIGURE 11 in Eriophyes species (Acari: Eriophyoidea) inhabiting lime trees (Tilia spp.: Tiliaceae) — supplementary description and morphological variability related to host plants and female forms
FIGURE 11. Digital micrographs of Eriophyes nervalis (Nalepa 1918). Protogyne female. A. Prodorsal shield; B. Coxigenital region (epigynium visible); C. Dorsal view of female posterior part; D. Female internal genitalia; E. Male genitalia, F. Ventral view of female posterior part. Scale bar: 20 µm for A and B; 10 µm for C, D, E & F.
FIGURE 5 in Eriophyes species (Acari: Eriophyoidea) inhabiting lime trees (Tilia spp.: Tiliaceae) — supplementary description and morphological variability related to host plants and female forms
FIGURE 5. Digital micrographs of Eriophyes exilis (Nalepa 1892). Nymph. A. Dorsal view of anterior region; B. Ventral view of anterior region. Scale bar: 10 µm for A & B.
FIGURE 10 in Eriophyes species (Acari: Eriophyoidea) inhabiting lime trees (Tilia spp.: Tiliaceae) — supplementary description and morphological variability related to host plants and female forms
FIGURE 10. Eriophyes nervalis (Nalepa 1918). Protogyne female. D. Dorsal view; SA. Lateral view of anterior region; CG. Coxigenital region; IG. Internal genitalia; L1. Leg I; L2. Leg II; em. Empodium (enlarged). Male. E. Epiandrium. Scale bar: 50 µm for D, SA, CG, E & IG; 25 µm for L1 & L2.
FIGURE 7 in Eriophyes species (Acari: Eriophyoidea) inhabiting lime trees (Tilia spp.: Tiliaceae) — supplementary description and morphological variability related to host plants and female forms
FIGURE 7. Erineum on leaf of Tilia tomentosa inhabited by Eriophyes exilis (Nalepa 1892) and Eriophyes nervalis (Nalepa 1918).
FIGURE 2 in Eriophyes species (Acari: Eriophyoidea) inhabiting lime trees (Tilia spp.: Tiliaceae) — supplementary description and morphological variability related to host plants and female forms
FIGURE 2. Digital micrographs of Eriophyes exilis (Nalepa 1892). Protogyne female. A. Prodorsal shield; B. Coxigenital region (epigynium visible); C. Dorsal view of female posterior region; D. Female internal genitalia; E. Male genitalia; F. Ventral view of female posterior region. Scale bar: 20 µm for A, B; 10 µm for C, D, E & F.
FIGURE 4. Notalina roraima Holzenthal 1986 in Notalina roraima Holzenthal 1986 (Trichoptera: Leptoceridae), male genitalia variability and larval description
FIGURE 4. Notalina roraima Holzenthal 1986, male genitalia of a Mt. Roraima specimen: A, dorsal; B, right inferior appendage, ventral; C, phallic apparatus, left lateral; D, phallic apparatus, ventral.
FIGURE 3. Notalina roraima Holzenthal 1986 in Notalina roraima Holzenthal 1986 (Trichoptera: Leptoceridae), male genitalia variability and larval description
FIGURE 3. Notalina roraima Holzenthal 1986, photographs of male genitalia of a Churí–tepui specimen: A, dorsal; B, ventral; photographs of the phallic apparatus of a Mt. Roraima specimen: C, ventral; D, left lateral; E, photograph of the case.
FIGURE 2. Notalina roraima Holzenthal 1986 in Notalina roraima Holzenthal 1986 (Trichoptera: Leptoceridae), male genitalia variability and larval description
FIGURE 2. Notalina roraima Holzenthal 1986, male genitalia of Churí–tepui specimen: A, left lateral; B, dorsal; C, phallic apparatus, left lateral; D, right inferior appendage, ventral.
FIGURE 5. Notalina roraima Holzenthal 1986 in Notalina roraima Holzenthal 1986 (Trichoptera: Leptoceridae), male genitalia variability and larval description
FIGURE 5. Notalina roraima Holzenthal 1986, larva: A, head, dorsal; B, labrum, dorsal; C, mandibles, ventral: D, head, ventral; E, thoracic sclerites, dorsal; F, right foreleg, right lateral (posterior); G, right middle leg, right lateral (posterior); H, right hind leg, right lateral (posterior); I, abdominal segment IX and abdominal prolegs, dorsal; J, right abdominal proleg and anal claw, right lateral.
FIGURE 9. Loxosceles mrazig, female genitalia variability. A, C, E in The Mediterranean species of genus Loxosceles Heineken & Lowe, 1832 (Araneae Sicariidae): Loxosceles imazighen sp. n. from Morocco and first description of the female of L. mrazig Ribera & Planas, 2009 from Tunisia
FIGURE 9. Loxosceles mrazig, female genitalia variability. A, C, E vulva of LX1899 (AL1), dorsal, ventral and anterior views; B, D, F vulva of LX2102 (TN2), dorsal, ventral and anterior views. IL = Inner lobe and OL = Outer lobe. Scale bars in mm.
FIGURE 10. Loxosceles mrazig, female genitalia variability. A, C, E in The Mediterranean species of genus Loxosceles Heineken & Lowe, 1832 (Araneae Sicariidae): Loxosceles imazighen sp. n. from Morocco and first description of the female of L. mrazig Ribera & Planas, 2009 from Tunisia
FIGURE 10. Loxosceles mrazig, female genitalia variability. A, C, E vulva of LX2107 (TN6), dorsal, ventral and anterior views; B, D, F vulva of LX2136 (TN14), dorsal, ventral and anterior views. IL = Inner lobe and OL = Outer lobe. Scale bars in mm.
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925). in Muridae
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925).
FIGURE 3. Bivariate probability density plot for the variables bracteole length and bracteole width. The isolines are 0.2 in Morphometric characterization of Eryngium viviparum (Umbelliferae): description of a new subspecies from the Iberian Peninsula
FIGURE 3. Bivariate probability density plot for the variables bracteole length and bracteole width. The isolines are 0.2 probability units apart, and those with a thicker line are the 1.0 and 2.0 levels. Note that although the three modes are clearly distinguishable, there is a large overlap between the Galician and French subpopulations.
FIGURE 5. A in Description of a geographically variable elongate rock-dwelling cichlid (Cichliformes: Cichlidae) from Lake Malaŵi, Africa
FIGURE 5. A male Metriaclima melissa at Mbuyu (A), at Chewere (B), and at Chirwa Island (C). A female M. melissa at Chewere (D), Lake Malaŵi, Malaŵi, Africa.
FIGURE 4. A in Description of a geographically variable elongate rock-dwelling cichlid (Cichliformes: Cichlidae) from Lake Malaŵi, Africa
FIGURE 4. A male Metriaclima melissa at the type locality Chitande Island, Lake Malaŵi, Malaŵi, Africa.
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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.