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2,474 results for “Northeast”
Figures 10–12 in Dentadra stigmatismena, a new species from Northeast India (Lepidoptera: Erebidae: Arctiinae: Lithosiini)
Figures 10–12. Lithosiina spp.: female genitalia. The specimens dissected are deposited in NHMUK (©The Trustees of NHMUK).
Figures 7–9 in Dentadra stigmatismena, a new species from Northeast India (Lepidoptera: Erebidae: Arctiinae: Lithosiini)
Figures 7–9. Lithosiina spp.: male genitalia. Depositories of the specimens dissected: 7 and 8 in NHMUK (©The Trustees of NHMUK); 9 in MWM/ZSM.
Figures 1–6 in Dentadra stigmatismena, a new species from Northeast India (Lepidoptera: Erebidae: Arctiinae: Lithosiini)
Figures 1–6. Lithosiina spp.: adults. The specimens are deposited in NHMUK (©The Trustees of NHMUK).
Fig. 1 in Natural enemies associated with Phaseolus lunatus L. (Fabaceae) in Northeast Brazil
Fig. 1. (A) Proctolaelaps bickleyi; (B) Amblyseius tamatavensi male, highlight for the long arrows; (C–D) Franklinothrips vespiformis; (E) emergence of Aphelinus sp. parasitizing Aphis craccivora; (F) Aphelinus sp. adult; (G) Pseudodorus clavatus larva; (H) Scymnus (Pullus) rubicundus egg; (I) S. rubicundus larva at different instars; (J) larva feeding on A. craccivora; (K) S. rubicundus adult.
Fig. 2 in Neglected parasite reservoirs in wetlands: Prevalence and diversity of avian haemosporidians in waterbird communities in Northeast China
Fig. 2. Diversity (a) and frequency (b) of haemosporidian parasite lineages obtained from waterbirds in Tumuji, China. Sankey diagrams of the correlation between waterbirds (left, sorted by order) and identified haemosporidian lineages (right). The width of the lines indicates proportion to the infection recordings in waterbirds, and the colour of the lines indicates the range of the lineage size. The numbers represent infection cases. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 3 in Neglected parasite reservoirs in wetlands: Prevalence and diversity of avian haemosporidians in waterbird communities in Northeast China
Fig. 3. Bayesian phylogenetic reconstruction of 479 bp haemosporidian cyt b lineages from waterbirds in Tumuji, China, with Hepatocystis sp. as an outgroup, and several morpho-species were included for a higher resolution of phylogenetic patterns. Posterior probabilities higher than 0.90 are shown by the node. Lineages that were previously recorded and detected in this study are marked in bold. Major monophyletic clades with high support are labelled behind the line (Leucocytozoon: L1-L5; Haemoproteus: H1–H3).
Fig. 1 in Neglected parasite reservoirs in wetlands: Prevalence and diversity of avian haemosporidians in waterbird communities in Northeast China
Fig. 1. Heatmap of the apparent prevalence of waterbird species in the Tumuji National Nature Reserve. Presenting infected waterbird species (left, sorted by order) with prevalence (indicated by colour gradient, scale from 0 to 1). The sample size is shown in parentheses.
Fig. 1 in Pleistocene non-passeriform landbirds from Shiriya, northeast Japan
Fig. 1. Geographic location of Shiriya localities. Landmarks mentioned in the text are also indicated. Inset (41°24'N, 141°24'E) shows major fossil localities mentioned in the text (stars; after Hasegawa et al. 1988). Dark grey indicates distribution of limestone/limestone breccia bodies (after Tsushima and Takizawa 1977). Abbreviations: I., island; Is., islands.
Fig. 5 in Pleistocene non-passeriform landbirds from Shiriya, northeast Japan
Fig. 5. Columbidae gen. et sp. indet. from the upper Pleistocene of Shiriya, Japan. A. NSMT PV 24551, right humerus in dorsal (A1) and cranial (A2) views. B. NSMT PV 24552, left humerus in cranial view. C. NSMT PV 24553 sternum in ventral (C1) and cranial (C2) views. Fossils coated with ammonium chloride.
Fig. 4 in Pleistocene non-passeriform landbirds from Shiriya, northeast Japan
Fig. 4. Coturnicini gen. et sp. indet. from the upper Pleistocene of Shiriya, Japan. A. NSMT PV 24543, right humerus in cranial (A1) and ventral (A2) views. B. NSMT PV 24547, tarsometatarsus in dorsal (B1) and medial (B2) views. C. NSMT PV 24545, left tibiotarsus in cranial view. Fossils coated with ammonium chloride. Abbreviation: c, concavity on the ventral surface of epicondylus ventralis (see text).
Fig. 10 in Pleistocene non-passeriform landbirds from Shiriya, northeast Japan
Fig. 10. Accipitridae gen. et sp. indet. from the upper Pleistocene of Shiriya, Japan. A. NSMT PV 19003, left femur in cranial (A1) and lateral A2) views. B. NSMT PV 24599, left ulna in craniodorsal (B1) and ventral B2) views. C. NSMT PV 24598, terminal phalanx of (right second?) pedal digit in lateral (C1) and medial (C2) views. Fossils coated with ammonium chloride. Scale bar 10 mm. Abbreviation: d, depression proximal to foramen pneumaticum (see text).
Fig. 6 in Pleistocene non-passeriform landbirds from Shiriya, northeast Japan
Fig. 6. Apodid bird Apus sp. from the upper Pleistocene of Shiriya, Japan (A, C, D), compared with Recent Apus pacificus (Latham, 1801) from Russia (B). A. NSMT PV 24548, left coracoids in ventral (A1) and dorsal (A2) views. B. UWBM 46958, left coracoid, in ventral (B1) and dorsal (B2) views; left carpometacarpus in dorsal view (B3); proximal phalanx of left major wing digit in dorsal view (B4). C. NSMT PV 24549, left carpometacarpus in ventral (C1) and dorsal (C2) views. D. NSMT PV 24550, proximal phalanx of right major wing digit in ventral (D1) and dorsal (D2) views. Fossils coated with ammonium chloride.
Fig. 2 in Pleistocene non-passeriform landbirds from Shiriya, northeast Japan
Fig. 2. Phasanid bird Syrmaticus sp. from the upper Pleistocene of Shiriya, Japan (A, B, E, F, H–L), compared with Recent Syrmaticus soemmerringii (Temminck, 1830) (C) and Recent Phasianus colchicus Linnaeus, 1758 (D). A. NSMT PV 24535, left humerus in cranial (A1) and caudal (A2) views. B. NSMT PV 24536, right humerus in cranial (B1) and caudal (B2) views. C. MVZ 49764, left humerus in caudal view (C1), left coracoid in dorsal (C2) and omal (C3) views, right carpometacarpus in dorsal view (C4). D. MVZ 68327, left humerus in caudal view (D1), left coracoid in dorsal (D2) and omal (D3) views. E, F. NSMT PV 24541 and NSMT PV 24542, respectively, right carpometacarpi in dorsal view. G. NSMT PV 24540, premaxilla in ventral (G1) and left lateral (G2) views. H. NSMT PV 24539, proximal phalanx of right major wing digit in dorsal (H1) and ventral (H2) views. I. Right ulnare (NSMT PV 24538), in distal (I1) and proximal (I2) views. J. Left coracoid (NSMT PV 24531), in ventral (J1), dorsal (J2), and omal (J3) views. K. Left coracoid (NSMT PV 24532), in ventral (K1) and dorsal (K2) views. Fossils coated with ammonium chloride.
Fig. 9 in Pleistocene non-passeriform landbirds from Shiriya, northeast Japan
Fig. 9. Bivariate scatter plots of Recent and fossil species of Haliaeetus: cranial (A), coracoidal (B), humeral (C), ulnar (D), radial (E), and tibiotarsal (F) measurements. Abbreviations: CNT, crista nuchalis transversa; FT, fossa temporalis.
Fig. 3 in Pleistocene non-passeriform landbirds from Shiriya, northeast Japan
Fig. 3. Bivariate scatter plots of Recent and fossil species of Syrmaticus: proximal (A) and distal (C) humeral, humeral shaft (B), and carpometacarpal (D) measurements.
Fig. 21 in Intraspecific variability in paradoxidid trilobites from the Purujosa trilobite assemblage (middle Cambrian, northeast Spain)
Fig. 21. Size-frequency distribution of 176 specimens of paradoxidid trilobite Eccaparadoxides pradoanus (Verneuil and Barrande in Prado et al., 1860) from the Purujosa trilobite assemblage, Solenopleuropsis thorali Biozone, middle Cambrian, Spain, sizes 2.5–67.5 mm in glabellar length. Size-frequency plot shows a normal distribution with some large specimens.
Fig. 20. A in Intraspecific variability in paradoxidid trilobites from the Purujosa trilobite assemblage (middle Cambrian, northeast Spain)
Fig. 20. A. Bivariate plot of first two first principal components in a sample of paradoxidid trilobite Eccaparadoxides pygidia from the Purujosa trilobite assemblage, Solenopleuropsis thorali Biozone, middle Cambrian, Spain, using six variables: anterior pygidial width, maximum pygidial width, posterior pygidial width, pygidial spine length (sagittal), pygidial spine length (exsagittal), and pygidial axial length (n = 99). B. Bivariate plot of principal components 2 and 3 (n = 99). Black circles, Eccaparadoxides pradoanus (Verneuil and Barrande in Prado et al., 1860) sensu Sdzuy 1961; white circles, Eccaparadoxides mediterraneus (Pompeckj, 1901) sensu Dies Álvarez et al. 2010.
Fig. 19. A in Intraspecific variability in paradoxidid trilobites from the Purujosa trilobite assemblage (middle Cambrian, northeast Spain)
Fig. 19. A. Bivariate plot of the first two principal components in a sample of paradoxidid trilobite Eccaparadoxides pradoanus (Verneuil and Barrande in Prado et al., 1860) cranidia from the Purujosa trilobite assemblage, Solenopleuropsis thorali Biozone, middle Cambrian, Spain, using four variables: glabellar length, palpebral lobe length, posterior glabellar width and anterior border length (n = 117). B. Bivariate plot of the principal components 2 and 3 in a sample of Eccaparadoxides cranidia from Purujosa trilobite assemblage using five variables: glabellar length, palpebral lobe length, posterior glabellar width and anterior border length and frontal area width (n = 46). Black circles, Eccaparadoxides pradoanus (Verneuil and Barrande in Prado et al., 1860) sensu Sdzuy 1961; white circles, Eccaparadoxides mediterraneus (Pompeckj, 1901) sensu Dies Álvarez et al. 2010; asterisk indicates lectotype.
Fig. 11 in Intraspecific variability in paradoxidid trilobites from the Purujosa trilobite assemblage (middle Cambrian, northeast Spain)
Fig. 11. Types of thoraxes in Eccaparadoxides pradoanus (Verneuil and Barrande in Prado et al., 1860) from the Purujosa trilobite assamblege, Solenopleuropsis thorali Biozone, middle Cambrian, Spain. A–C. Heteronomous thorax. D. Homonomous thorax. See text for explanation. Scale bars 5 mm.
Fig. 6 in Intraspecific variability in paradoxidid trilobites from the Purujosa trilobite assemblage (middle Cambrian, northeast Spain)
Fig. 6. Relationship between angles in S1 and the glabellar length in paradoxidid trilobite Eccaparadoxides pradoanus (Verneuil and Barrande in Prado et al., 1860) from the Purujosa trilobite assemblage, Solenopleuropsis thorali Biozone, middle Cambrian, Spain (for angles taken see Fig. 2).
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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.