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FIG. 2 in New records of bopyrid parasites (Crustacea, Isopoda, Epicaridea) of pea crabs (Crustacea, Decapoda, Pinnotheridae) with descriptions of two new species of Rhopalione Pérez, 1921 and a review of the genus
FIG. 2. — Heterocepon marginatum Shiino, 1936, ZRC 2023.0271 (A-I): A, right antenna and antennule of female; B, barbula of female (asterisk shows missing outer lobe); C, left maxilliped of female, outer view with outer barbular lobe attached; D, left oostegite 1 of female, outer view; E, left oostegite 1 of female, inner view; F, left pereopod 1 of female; G, left pereopod 7 of female. Scale bars: A, F, G, 50 µm; B, 250 µm; C-E, 200 µm.
FIG. 7 in New records of bopyrid parasites (Crustacea, Isopoda, Epicaridea) of pea crabs (Crustacea, Decapoda, Pinnotheridae) with descriptions of two new species of Rhopalione Pérez, 1921 and a review of the genus
FIG. 7. — Rhopalione sinensis Markham, 1990 (NHMD-1184775): A, female, dorsal view; B, female, lateral view; C, left oostegite 1, inner view; D, left maxilliped, outer view. Scale bars: A, B, 2 mm; C, D, 100 µm.
FIG. 6 in New records of bopyrid parasites (Crustacea, Isopoda, Epicaridea) of pea crabs (Crustacea, Decapoda, Pinnotheridae) with descriptions of two new species of Rhopalione Pérez, 1921 and a review of the genus
FIG. 6. — Rhopalione atrinicolae Page, 1985 paratype specimens (A, B: NMNZ Cr. 3090) and non-type specimens (C, D: NIWA 160626): A, female, dorsal view; B, male, dorsal view. C, female, dorsal view; D, female, dorsal view, arrow shows lateral plate with slightly crenulate edge. Scale bars: A, C, D, 2 mm; B, 1 mm.
FIG. 5 in New records of bopyrid parasites (Crustacea, Isopoda, Epicaridea) of pea crabs (Crustacea, Decapoda, Pinnotheridae) with descriptions of two new species of Rhopalione Pérez, 1921 and a review of the genus
FIG. 5. — Rhopalione uromyzon Pérez, 1920:two syntype males (MNHN-IU-2024-3189) (A-C, E-G: 3.45 mm, D: 3.68 mm), one syntype female (MNHN-IU-2024-3196) (H, 3.90 mm), 2 syntype females (I, 4.35 mm, J, 5.55 mm): A, dorsal view; B, lateral view; C, ventral view; D, dorsal view, E, left antennule and antenna; F, left pereopod 1; G, left pereopod 7; H-J, dorsal views. Scale bars: A-D, H, 500 µm; E-G, 100 µm; I, J, 1 mm.
FIG. 1 in New records of bopyrid parasites (Crustacea, Isopoda, Epicaridea) of pea crabs (Crustacea, Decapoda, Pinnotheridae) with descriptions of two new species of Rhopalione Pérez, 1921 and a review of the genus
FIG. 1. — Heterocepon marginatum Shiino, 1936, ZRC 2023.0264 (A), ZRC 2023.0269 (B), SMF-ZMG948b (C, D): A, female, dorsal view (dashed line shows where oostegites are cut-off in the picture); B, male, dorsal view; C, female in host Arcotheres palaensis (Bürger, 1895); D, female, dorsal view. Scale bars: A, B, D, 1 mm; C, 2.5 mm.
FIG. 10. — Rhopalione rusa n in New records of bopyrid parasites (Crustacea, Isopoda, Epicaridea) of pea crabs (Crustacea, Decapoda, Pinnotheridae) with descriptions of two new species of Rhopalione Pérez, 1921 and a review of the genus
FIG. 10. — Rhopalione rusa n. sp. holotype (ZRC 2023.0259) and allotype (ZRC 2023.0260) specimens: A, ventral view of host pinnotherid Arcotheres similis (Bürger, 1895) with Rhopalione sp. in situ on left side of pleon (posterior end of male shown by arrow); B, holotype female, dorsal view; C, holotype female, ventral view; D, allotype male, dorsal view. Scale bars: A, 2 mm; B-D, 1 mm.
FIG. 9. — Rhopalione racemus n in New records of bopyrid parasites (Crustacea, Isopoda, Epicaridea) of pea crabs (Crustacea, Decapoda, Pinnotheridae) with descriptions of two new species of Rhopalione Pérez, 1921 and a review of the genus
FIG. 9. — Rhopalione racemus n. sp. holotype (A-H) and allotype (I-L) specimens (SAM C16386): A, left antennae; B, barbula; C, left maxilliped, with base of barbular lobes shown; D, left oostegite 1, outer view; E, left oostegite 1, inner view; F, pereomere 7 and pleon, ventral view; G, left pereopod 1 and coxal plate; H, left pereopod 7; I, ventral view; J, right antennae, oral cone and maxilliped; K, right pereopod 1; L, left pereopod 7. Abbreviations: CP, coxal plate; IL, inner barbular lobe; Max, maxilliped; OL, outer barbular lobe; Or, oral cone. Scale bars: A, G, H, 100 µm; B, D, E, I, 500 µm; C, 250 µm; F, 1 mm; J-L, 50 µm.
Fig. 12. Distribution records for E in Taxonomic revision of the oil-collecting bee subgenus Epicharis (Epicharitides) Moure, 1945 (Hymenoptera: Apidae), with the description of two new species
Fig. 12. Distribution records for E. lia sp. nov., E. mesoamericana sp. nov. and E. rufescens Moure & Seabra, 1959.
Fig. 11 in Taxonomic revision of the oil-collecting bee subgenus Epicharis (Epicharitides) Moure, 1945 (Hymenoptera: Apidae), with the description of two new species
Fig. 11. Distribution records for Epicharis luteocincta Moure & Seabra, 1959, E. minima (Friese, 1904) and E. obscura Friese, 1899. Symbols with a cross represent records from literature.
Fig. 9 in Taxonomic revision of the oil-collecting bee subgenus Epicharis (Epicharitides) Moure, 1945 (Hymenoptera: Apidae), with the description of two new species
Fig. 9. Epicharis (Epicharitides) rufescens Moure & Seabra, 1959. A–B. Paratype, ♀ (Brazil: Óbidos; MNRJ). A. Head, frontal view. B. Habitus, lateral view. C–D. Paratype, ♂ (Brazil: Óbidos; MNRJ). C. Head, frontal view. D. Habitus, lateral view. Scale bars: A, C = 1 mm; B, D = 5 mm.
Fig. 2 in Taxonomic revision of the oil-collecting bee subgenus Epicharis (Epicharitides) Moure, 1945 (Hymenoptera: Apidae), with the description of two new species
Fig. 2. Epicharis (Epicharitides) duckei Friese, 1901. A–B. Female (Brazil: Nova Mutum; INPA). A. Head, frontal view. B. Habitus, lateral view. C–D. Male (Brazil: Belém; MPEG). C. Head, frontal view. D. Habitus, lateral view. Scale bars: A, C = 1 mm; B, D = 5 mm.
Fig. 6 in Taxonomic revision of the oil-collecting bee subgenus Epicharis (Epicharitides) Moure, 1945 (Hymenoptera: Apidae), with the description of two new species
Fig. 6. Epicharis (Epicharitides) mesoamericana sp. nov., holotype, ♀ (Mama Noots, Stann Creek, Belize; AMNH). A. Head, frontal view. B. Habitus, lateral view. Scale bars: A = 1 mm; B = 5 mm.
Fig. 5 in Taxonomic revision of the oil-collecting bee subgenus Epicharis (Epicharitides) Moure, 1945 (Hymenoptera: Apidae), with the description of two new species
Fig. 5. Epicharis (Epicharitides) luteocincta Moure & Seabra, 1959. A–B. Female (Brazil: Itirapina; CEPANN). A. Head, frontal view. B. Habitus, lateral view. C–D. Male (Brazil: São Paulo; CEPANN). C. Head, frontal view. D. Habitus, lateral view. Scale bars: A, C = 1 mm; B, D = 5 mm.
Fig. 8 in Taxonomic revision of the oil-collecting bee subgenus Epicharis (Epicharitides) Moure, 1945 (Hymenoptera: Apidae), with the description of two new species
Fig. 8. Epicharis (Epicharitides) obscura Friese, 1899. A–B. Female (Brazil: Mogi das Cruzes; CEPANN). A. Head, frontal view. B. Habitus, lateral view. C–D. Male (Brazil: Santa Teresa; HNHM). C. Head, frontal view. D. Habitus, lateral view. Scale bars: A, C = 1 mm; B, D = 5 mm.
Fig. 10. Distribution records for Epicharis cockerelli Friese, 1900, E. duckei Friese, 1901 and E. iheringi Friese, 1899. Symbols with a in Taxonomic revision of the oil-collecting bee subgenus Epicharis (Epicharitides) Moure, 1945 (Hymenoptera: Apidae), with the description of two new species
Fig. 10. Distribution records for Epicharis cockerelli Friese, 1900, E. duckei Friese, 1901 and E. iheringi Friese, 1899. Symbols with a cross represent records from literature.
Fig. 4 in Taxonomic revision of the oil-collecting bee subgenus Epicharis (Epicharitides) Moure, 1945 (Hymenoptera: Apidae), with the description of two new species
Fig. 4. Epicharis (Epicharitides) lia sp. nov., holotype, ♀ (Peru: Pilcopata; MNRJ). A. Head, frontal view. B. Habitus, lateral view. Scale bars: A = 1 mm; B = 5 mm.
Fig. 1 in Taxonomic revision of the oil-collecting bee subgenus Epicharis (Epicharitides) Moure, 1945 (Hymenoptera: Apidae), with the description of two new species
Fig. 1. Epicharis (Epicharitides) cockerelli Friese, 1900. A–B. Female (Brazil: Passos; DZMG). A. Head, frontal view. B. Habitus, lateral view. C–D. Male (Brazil: Passos; DZMG). C. Head, frontal view. D. Habitus, lateral view. Scale bars: A, C = 1 mm; B, D = 5 mm.
Fig. 3 in Taxonomic revision of the oil-collecting bee subgenus Epicharis (Epicharitides) Moure, 1945 (Hymenoptera: Apidae), with the description of two new species
Fig. 3. Epicharis (Epicharitides) iheringi Friese, 1899. A–B. Female (Brazil: Cássia dos Coqueiros; RPSP). A. Head, frontal view. B. Habitus, lateral view. C–D. Male (Brazil: Varginha; MNRJ). C. Head, frontal view. D. Habitus, lateral view. Scale bars: A, C = 1 mm; B, D = 5 mm.
Fig. 7 in Taxonomic revision of the oil-collecting bee subgenus Epicharis (Epicharitides) Moure, 1945 (Hymenoptera: Apidae), with the description of two new species
Fig. 7. Epicharis (Epicharitides) minima (Friese, 1904). A–B. Female (Brazil: Vilhena; MNRJ). A. Head, frontal view. B. Habitus, lateral view. C–D. Male (Brazil: Cajuru; RPSP). C. Head, frontal view. D. Habitus, lateral view. Scale bars: A, C = 1 mm; B, D = 5 mm.
Concrete habitat: Impervious surface in nest vicinity is associated with avian fitness decline in two urban adapters
<p>The conversion of natural habitats to impervious surfaces in cities affects biotic and abiotic attributes of urban ecosystems. Detailed information on the gradual influence of impervious surfaces on reproductive success, however, is lacking. Using five years of nestbox-breeding great tit and blue tit breeding data collected across various habitat types within and outside a Central-Eastern European capital city, we quantified the impact of impervious surfaces on avian reproductive success. Impervious surfaces strongly and negatively covaried with the number of fledged young in both species: a 50% increase in impervious surface resulted in 2.93 (95% CI: -4.27; -1.58) fewer blue tit offspring fledging the nest, and 3.51 (95% CI: -4.79; -2.23) fewer great tit offspring fledging the nest, thus halving the reproductive output of two widespread urban species. These results provide benchmark values of avian productivity for ecologists and urban policy makers, and for the management of urban areas.</p>
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.