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FIG. 7 in Contribution à la connaissance des Tetrigidae (Orthoptera) de Guyane
FIG. 7. — Station du Rorota: A, sentier sur lequel ont été trouvés les individus d'Allotettix cayennensis (Bolívar, 1887) et Eomorphopus granulatus Hancock, 1907; B, mâle d'Eomorphopus granulatus et son fémur médian foliacé; C, femelle d'Eomorphopus granulatus (notez sa coloration qui se confond parfaitement avec son environnement!); D, mâle d'Allotettix cayennensis. Photos: G. Doucet & R. Itrac-Bruneau.
FIG. 5. — Tettigidea claudei n in Contribution à la connaissance des Tetrigidae (Orthoptera) de Guyane
FIG. 5. — Tettigidea claudei n. sp. allotype ♀, MNHN-EO-CAELIF10727: A, habitus en vue latérale; B, habitus en vue dorsale; C, individu taille réelle; D, tête vue de face; E, tête et pronotum en vue dorsale; F, tête et pronotum en vue latérale; G, extrémité de l'abdomen en vue ventrale; H, extrémité de l'abdomen en vue latérale. Photos: G. Doucet. Échelles: A, B, D-F, 1 mm; C, 1 cm; G, H, 0,5 mm.
FIG. 4. — Tettigidea claudei n in Contribution à la connaissance des Tetrigidae (Orthoptera) de Guyane
FIG. 4. — Tettigidea claudei n. sp. holotype ♂, MNHN-EO-CAELIF10726: A, habitus en vue latérale; B, habitus en vue dorsale; C, individu taille réelle; D, tête vue de face; E, tête et pronotum en vue dorsale; F, tête et pronotum en vue latérale; G, extrémité de l'abdomen en vue dorsale; H, extrémité de l'abdomen en vue latérale. Photos: G. Doucet. Échelles: A, B, 1 mm; C, 1 cm; D-H, 0,5 mm.
FIG. 2 in Contribution à la connaissance des Tetrigidae (Orthoptera) de Guyane
FIG. 2. — Mesures de différents paramètres sur un individu ♀ de Tettigidea claudei n. sp.: A, distance entre la marge antérieure du pronotum et le sinus tegminal (DPT) et longueur du tegmen (LT); B, longueur de la plaque sous-génitale (LPSG) et longueur du dépassement de la valve ventrale (LDVV). Photos: G. Doucet.
Figs 22–25 in Contribution To The Taxonomy And Phylogeny Of The Genus Polia Ochsenheimer, 1816 (Noctuidae, Noctuinae, Hadenini): Species Groups And Pairs In The Holarctic Subgenus Polia S. Str.
Figs 22–25. Female genitalia of Polia species: 22 = P. hepatica (Clerck, 1759), slide no. RL12394, Austria, 23 = P. vespertilio (Draudt, 1934), slide no. VZ9972, Russia, Transbaikalia, 24 = P. imbrifera (Guenée, 1852), slide no. VZ9969, Canada, 25 = P. lama (Staudinger, 1896), slide no. RL12347, Kirghisia
Pollination deficits and contributions of pollinators in apple production: a global meta-analysis
<p>1. Apple is one of the most widely cultivated fruit crops worldwide, and apple yield benefits from pollination by insects. The global decline in wild pollinator populations raises concern about the adequacy of pollination services in apple production.</p> <p>2. Here, we present a global meta-analysis of pollination in apple. We assembled from the literature a dataset comprising results of 48 studies across five continents on fruit set and seed set in apple with insect pollination, artificial pollination and pollinator exclusion, and analysed the effects of explanatory factors such as variety and continent.</p> <p>3. Fruit set was on average 41% lower with open pollination than with artificial pollination, while seed set was 20% lower. These pollination deficits varied across continents and cultivars. Pollination deficits for fruit set were greatest in Asia (63%) followed by Europe (30%), whereas pollination deficits for seed set were greatest in Asia (47%) and South America (40%). Important differences in pollination deficit were also identified between cultivars but these differences were confounded with continent effects.</p> <p>4. Fruit set and seed set were 71% and 62% higher, respectively, when insects had open access to flowers than when they were artificially excluded, while results varied among cultivars.</p> <p>5. Synthesis and Applications. Globally, there are substantial contributions of pollinators to fruit set and seed set in apple, as well as considerable limitations in apple pollination services, particularly in Asia, Europe and South America. Several management strategies could be applied to reduce the pollination deficits in apple production: (1) conserving wild bees and enhancing their abundance and diversity, (2) using managed bees for pollination, (3) using varieties with low pollinator dependency, and/or (4) artificial pollination. These strategies should be tailored to the regional situation, considering the potential of landscapes for restoring wild pollinators, the acceptability of cultivated varieties for available pollinators, the acceptance in the market of self-compatible varieties, and the costs of management, such as artificial pollination, pollinator conservation, beekeeping and planting self-compatible varieties. Conservation of wild pollinators is preferred in regions with sufficient potential for wild pollinators as it contributes to biodiversity conservation and improves pollination in both crops and wild plants.</p>
Figure 2 in The chennelli group of the Genus Therates Latreille (Coleoptera: Cicindelidae) 114. Contribution towards the knowledge of Cicindelidae
Figure 2. Characteristics (1 to 14) used for evaluating homogenities (1 to 53) and the resultant data matrix.
Fig. 64. Cyparium oberthueri Pic, 1956 in Contributions to the taxonomy of Neotropical Cyparium Erichson (Coleoptera: Staphylinidae: Scaphidiinae), with the description of five new species
Fig. 64. Cyparium oberthueri Pic, 1956 (MNHN collection-Paris).A. Habitus. B. Labels.C. Distribution. Squares = P. Germain itinerary; circles = new records.
Fig. 61. Cyparium oberthueri Pic, 1956 in Contributions to the taxonomy of Neotropical Cyparium Erichson (Coleoptera: Staphylinidae: Scaphidiinae), with the description of five new species
Fig. 61. Cyparium oberthueri Pic, 1956, ♂♂ (CELC). A–B. Abdomen. A. Dorsal view. B. Ventral view. C. Ventrite 1. D. Tergite VIII. E. Terminalia. F. Tergite IX. G. Sternite VIII. Specimens collected at Mata da Biologia, Viçosa (MG, Brazil). Scale bars: A, C–G = 0.2 mm; B = 0.5 mm.
Fig. 60. Cyparium oberthueri Pic, 1956 in Contributions to the taxonomy of Neotropical Cyparium Erichson (Coleoptera: Staphylinidae: Scaphidiinae), with the description of five new species
Fig. 60. Cyparium oberthueri Pic, 1956, ♂♂ (CELC). A–B. Metendosternite. A. Dorsal view. B. Lateral view. C–D. Elytron. C. Entire. D. Apex. E. Hind wing. F–H. Legs. F. Fore. G. Middle. H. Hind. Specimens collected at Mata da Biologia, Viçosa (MG, Brazil). Scale bars = 0.5 mm.
Fig. 57. Cyparium oberthueri Pic, 1956 in Contributions to the taxonomy of Neotropical Cyparium Erichson (Coleoptera: Staphylinidae: Scaphidiinae), with the description of five new species
Fig. 57. Cyparium oberthueri Pic, 1956 (CELC). A. Frontal view. B. Male antenna. C. Female antenna. D. Labrum. E. Left mandible. F. Right mandible. G. Maxilla. Specimens collected at Mata da Biologia, Viçosa (MG, Brazil) (CELC). Scale bars: A–C = 0.2 mm; D–G = 0.1 mm.
Fig. 54. Cyparium collare Pic, 1920 in Contributions to the taxonomy of Neotropical Cyparium Erichson (Coleoptera: Staphylinidae: Scaphidiinae), with the description of five new species
Fig. 54. Cyparium collare Pic, 1920, ♀ (CELC). A. Tergite VIII. B. Sternite VIII. C. Terminalia. D. Sclerite of vaginal plate. E. Ovipositor. Specimen collected at Mata do Paraíso, Viçosa (MG, Brazil). Scale bars: A–B, D–E = 0.1 mm; C = 0.2 mm.
Fig. 52. Cyparium collare Pic, 1920 in Contributions to the taxonomy of Neotropical Cyparium Erichson (Coleoptera: Staphylinidae: Scaphidiinae), with the description of five new species
Fig. 52. Cyparium collare Pic, 1920, ♂♂ (CELC). A–B. Abdomen. A. Dorsal view. B. Ventral view. C. Ventrite 1. D. Tergite VIII. E. Terminalia. F. Tergite IX. G. Sternite VIII. Specimens collected at Mata do Paraíso, Viçosa (MG, Brazil). Scale bars = 0.2 mm.
Fig. 49. Cyparium collare Pic, 1920 in Contributions to the taxonomy of Neotropical Cyparium Erichson (Coleoptera: Staphylinidae: Scaphidiinae), with the description of five new species
Fig. 49. Cyparium collare Pic, 1920, ♂♂ (CELC). A. Labium. B. Hypopharynx. C. Head, ventral view. D–E. Pronotum, dorsal view. F–G. Prothorax. F. Ventral view. G. Inner view. Specimens collected at Mata do Paraíso, Viçosa (MG, Brazil). Scale bars: A–C = 0.1 mm; D–G = 0.2 mm.
Fig. 47. Cyparium collare Pic, 1920. A–C in Contributions to the taxonomy of Neotropical Cyparium Erichson (Coleoptera: Staphylinidae: Scaphidiinae), with the description of five new species
Fig. 47. Cyparium collare Pic, 1920. A–C. ♂ (CELC). A. Dorsal view. B. Ventral view. C. Lateral view. D–F. ♀ (CELC). D. Dorsal view. E. Lateral view. F. Dorsal view. Specimens collected at Mata do Paraíso (A–C) and Mata da Biologia (D–F), Viçosa (MG, Brazil). Scale bars = 1.0 mm.
Fig. 46. A in Contributions to the taxonomy of Neotropical Cyparium Erichson (Coleoptera: Staphylinidae: Scaphidiinae), with the description of five new species
Fig. 46. A. Distribution map of species of Cyparium Erichson, 1845, South America. B. Mata da Biologia. C. Mata do Paraíso.
Fig. 41 in Contributions to the taxonomy of Neotropical Cyparium Erichson (Coleoptera: Staphylinidae: Scaphidiinae), with the description of five new species
Fig. 41. Cyparium pici sp. nov., paratype, ♂ (CELC). A. Prothorax, lateral view. B–C. Scutellar plate. B. Dorsal view. C. Apically slanted view. D–E. Meso- and metathorax. D. Ventral view. E. Lateral view. F. Metanotum. Specimen collected at Cotriguaçu (MT, Brazil). Scale bars: A, D–F = 0.5 mm; B–C = 0.1 mm.
Fig. 40 in Contributions to the taxonomy of Neotropical Cyparium Erichson (Coleoptera: Staphylinidae: Scaphidiinae), with the description of five new species
Fig. 40. Cyparium pici sp. nov. A–C. Paratype, ♂ (CELC). A. Labium. B. Hypopharynx. C. Head, ventral view. D. Holotype, ♂ (CEMT), pronotum, dorsal view. E. Paratype, ♂ (CEMT), pronotum, dorsal view. F–G. Paratype, ♂ (CELC), prothorax. F. Ventral view. G. Inner view. Specimens collected at Cotriguaçu (MT, Brazil). Scale bars: A–B = 0.1 mm; C = 0.2 mm; D–G = 0.5 mm.
Fig. 63. Cyparium oberthueri Pic, 1956 in Contributions to the taxonomy of Neotropical Cyparium Erichson (Coleoptera: Staphylinidae: Scaphidiinae), with the description of five new species
Fig. 63. Cyparium oberthueri Pic, 1956, ♀ (CELC). A. Tergite VIII. B. Sternite VIII. C. Terminalia. D. Sclerite of vaginal plate. E. Ovipositor. Specimen collected at Mata da Biologia, Viçosa (MG, Brazil). Scale bars: A–C, E = 0.2 mm; D = 0.1 mm.
Fig. 53. Cyparium collare Pic, 1920 in Contributions to the taxonomy of Neotropical Cyparium Erichson (Coleoptera: Staphylinidae: Scaphidiinae), with the description of five new species
Fig. 53. Cyparium collare Pic, 1920, ♂ (CELC). A–C. Aedeagus. A. Lateral view. B. Frontal view. C. Dorsal view. D–E. Internal sac. D. Frontal view. E. Dorsal view. Specimen collected at Mata do Paraíso, Viçosa (MG, Brazil). Scale bars = 0.1 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.