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FIGURE 1 in Description of Chironomus quinnitukut, n. sp., closely related to the C. decorus group in North America, with characterization of an additional larval form from halobiontic habitats
FIGURE 1. Male genitalia of C. quinnitukqut: a. dorsal view, b. inferior volsellae, c. apodemes, d. phallapodeme and pars centralis - 1. Note the double "fulcrum" on the transverse sternapodeme, and 2. Ventral portal setae.
FIGURE 5 in On the evolution of the species complex Pachycondyla chinensis (Hymenoptera: Formicidae: Ponerinae), including the origin of its invasive form and description of a new species
FIGURE 5. Characters of male coloration and mandible of P. nakasujii (A, B), P. chinensis (C, D) and P. luteipes (E, F). Black arrows indicate the mandible.
FIGURE 6 in On the evolution of the species complex Pachycondyla chinensis (Hymenoptera: Formicidae: Ponerinae), including the origin of its invasive form and description of a new species
FIGURE 6. Currently known distribution of P. nakasujii (A) and P. chinensis (B) in Japan. Each dot may indicate more than one site if they are located less than 20 km apart.
FIGURE 2 in On the evolution of the species complex Pachycondyla chinensis (Hymenoptera: Formicidae: Ponerinae), including the origin of its invasive form and description of a new species
FIGURE 2. Mean (± SD) of the biometric measurements of P. nakasujii and P. chinensis (n = 13 and 35, respectively).
FIGURE 4 in On the evolution of the species complex Pachycondyla chinensis (Hymenoptera: Formicidae: Ponerinae), including the origin of its invasive form and description of a new species
FIGURE 4. Characters of worker propodeum and petiole. The left side of worker propodeum and petiole of P. nakasujii (A), P. chinensis (C) and P. luteipes (E), and the posterior face of worker petiole of P. nakasujii (B), P. chinensis (D) and P. luteipes (F) (Scanning electron microscopy photographs). Horizontal white arrow: PW. Also see Japanese Ant Database Group (2003).
FIGURE 1 in On the evolution of the species complex Pachycondyla chinensis (Hymenoptera: Formicidae: Ponerinae), including the origin of its invasive form and description of a new species
FIGURE 1. Bayesian phylogenetic tree of the species complex Pachycondyla chinensis based on mitochondrial sequences of the COI region. The corresponding posterior probabilities (≥0.70) are shown by the branch. The horizontal bar represents a distance of 0.1 substitutions per site. GenBank accession numbers are shown in parentheses.
FIGURE 8. Shield forms from L3 in Nematodes from galls on Myrtaceae. IV. Fergusobia from flat leaf galls on Eucalyptus and Corymbia, with descriptions of two new species
FIGURE 8. Shield forms from L3 larvae of Fergusonina spp. from flat leaf galls (automontage images): A, from E. odorata; B, from E. siderophloia; C, from E. porosa. Scale bars = 0.5 mm.
FIGURE 4. Form I in Cambarus (C.) hatfieldi, a new species of crayfish (Decapoda: Cambaridae) from the Tug Fork River Basin of Kentucky, Virginia and West Virginia, USA
FIGURE 4. Form I gonopod's of (A.) Cambarus hatfieldi, (B.) Cambarus sciotensis, and (C.) Cambarus angularis.
FIGURE 23 in Eriophyes species (Acari: Eriophyoidea) inhabiting lime trees (Tilia spp.: Tiliaceae) — supplementary description and morphological variability related to host plants and female forms
FIGURE 23. Canonical variate analysis of 43 traits for protogynes and deutogynes of Eriophyes nervalis Nalepa 1890 carried out on pooled data collected from Tilia tomentosa and T. platyphyllos over two seasons.
FIGURE 24 in Eriophyes species (Acari: Eriophyoidea) inhabiting lime trees (Tilia spp.: Tiliaceae) — supplementary description and morphological variability related to host plants and female forms
FIGURE 24. Canonical variate analysis of 43 traits for protogynes and deutogynes of Eriophyes tiliae Nalepa 1890 carried out on pooled data collected from Tilia americana, T. cordata and T. platyphyllos.
FIGURE 22 in Eriophyes species (Acari: Eriophyoidea) inhabiting lime trees (Tilia spp.: Tiliaceae) — supplementary description and morphological variability related to host plants and female forms
FIGURE 22. Canonical variate analysis of 43 traits for protogyne and deutogyne female forms of Eriophyes exilis (Nalepa 1892) carried out on pooled data collected from Tilia tomentosa and T. platyphyllos species and two seasons.
FIGURE 18 in Eriophyes species (Acari: Eriophyoidea) inhabiting lime trees (Tilia spp.: Tiliaceae) — supplementary description and morphological variability related to host plants and female forms
FIGURE 18. Digital micrographs of Eriophyes tiliae Nalepa 1890. Deutogyne female. A. Prodorsal shield; B. Coxigenital region (epigynium visible); C. Dorsal view of posterior region; D. Internal genitalia; E. Legs I and II; F. Ventral view of posterior region. Scale bar: 10 µm for A, B, C, D, E & F.
FIGURE 13 in Eriophyes species (Acari: Eriophyoidea) inhabiting lime trees (Tilia spp.: Tiliaceae) — supplementary description and morphological variability related to host plants and female forms
FIGURE 13. Digital micrographs of Eriophyes nervalis (Nalepa 1918). Deutogyne female. A. Prodorsal shield; B. Coxigenital region (epigynium visible); C. Dorsal view of posterior region; d. Internal genitalia; E. Legs I and II; F. Ventral view of posterior region. Scale bar: 10 µm for A, B, C, D, E & F.
FIGURE 16 in Eriophyes species (Acari: Eriophyoidea) inhabiting lime trees (Tilia spp.: Tiliaceae) — supplementary description and morphological variability related to host plants and female forms
FIGURE 16. Digital micrographs of Eriophyes tiliae Nalepa 1890. Protogyne female. A. Prodorsal shield; B. Coxigenital region (epigynium visible); C. Dorsal view of posterior region; D. Female internal genitalia; E. Male genitalia; F. Ventral view of posterior region. Scale bar: 10 µm for A, B, C, D, E & F.
FIGURE 8 in Eriophyes species (Acari: Eriophyoidea) inhabiting lime trees (Tilia spp.: Tiliaceae) — supplementary description and morphological variability related to host plants and female forms
FIGURE 8. Erineum nervale on leaf of Tilia cordata inhabited by Eriophyes exilis (Nalepa 1892) and E. nervalis (Nalepa 1918).
FIGURE 4 in Eriophyes species (Acari: Eriophyoidea) inhabiting lime trees (Tilia spp.: Tiliaceae) — supplementary description and morphological variability related to host plants and female forms
FIGURE 4. Digital micrographs of Eriophyes exilis (Nalepa 1892). Deutogyne female. A. Prodorsal shield; B. Coxigenital region (epigynium visible); C. Dorsal view of posterior region; D. Internal genitalia; E. Leg I and leg II; F. Ventral view of posterior region; Scale bar: 20 µm for A & B; 10 µm for C, D, E & F.
FIGURE 1 in Eriophyes species (Acari: Eriophyoidea) inhabiting lime trees (Tilia spp.: Tiliaceae) — supplementary description and morphological variability related to host plants and female forms
FIGURE 1. Eriophyes exilis (Nalepa 1892). 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 9 in Eriophyes species (Acari: Eriophyoidea) inhabiting lime trees (Tilia spp.: Tiliaceae) — supplementary description and morphological variability related to host plants and female forms
FIGURE 9. Erineum on leaf lower surface of Tilia cordata inhabited by Eriophyes exilis (Nalepa 1892) and E. nervalis (Nalepa 1918).
FIGURE 12 in Eriophyes species (Acari: Eriophyoidea) inhabiting lime trees (Tilia spp.: Tiliaceae) — supplementary description and morphological variability related to host plants and female forms
FIGURE 12. Eriophyes nervalis (Nalepa 1918). 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 17. Eriophyes tiliae Nalepa 1890. Deutogyne 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 17. Eriophyes tiliae Nalepa 1890. 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.
ScienceDex guides
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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.