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Fig. 4 in New Hesionidae (Annelida) from Japan: Unavailable Names Introduced by Uchida (2004) Revisited, with Reestablishment of their Availability
Fig. 4. Photographs of live specimens of four species of Oxydromus. A, B, O. bunbuku sp. nov.: A, holotype (NSMT-Pol H-693); B, paratype (NSMT-Pol P-695) associated with the spatangoid urchin Brissus latecarinatus. C, D, O. constrictus sp. nov.: C, holotype (NSMT-Pol H-698); D, nontype (UAM Pol-1-12-6-1-A) crawling among spines of the host sea urchin (photograph by Dr. Daisuke Uyeno). E, O. fauveli sp. nov., paratype (NSMT-Pol P-707). F, O. parapallidus sp. nov., paratype (NSMT-Pol P-737).
Fig. 5 in New Hesionidae (Annelida) from Japan: Unavailable Names Introduced by Uchida (2004) Revisited, with Reestablishment of their Availability
Fig. 5. Oxydromus constrictus sp. nov., holotype (NSMT-Pol H-698). A, dorsal view of the anterior body. B, dorsal view of the posterior end. C, posterior view of left parapodium 17, with a short notocirrus. D, anterior view of left parapodium 22, with a long notocirrus. E, posterior view of the same parapodium. F, posterior view of left parapodium 23, with a short notocirrus. G, superior supra-acicular neuropodial compound falciger. H, median supra-acicular falciger. I, inferior supra-acicular falciger. J, median sub-acicular falciger. K, inferiormost subacicular falciger. Scale bars: 1 mm for A, B; 0.5 mm for C, D, F; 0.2 mm for E; 0.05 mm for G–K.
Fig. 1 in New Hesionidae (Annelida) from Japan: Unavailable Names Introduced by Uchida (2004) Revisited, with Reestablishment of their Availability
Fig. 1. Synsyllidia alternata gen. et sp. nov., holotype (NSMT-Pol H-691). A, dorsal view of the anterior body. B, enlarged dorsal view of the anterior end, showing the everted proboscis, prostomium, and the following segments. C, ventral view of the anterior end. D, anterior view of right parapodium 9. E, posterior view of the same. F, notopodial cirrophore in the same parapodium, with notoacicula. G, neuropodial acicula and a simple chaeta in the same parapodium. H, superiormost compound falciger. I, median falciger. J, inferiormost two falcigers. K, tip of simple chaeta. Scale bar: 0.5 mm for A; 0.2 mm for B–D; 0.1 mm for E; 0.05 mm for F–J; 0.02 mm for K.
Fig. 3 in New Hesionidae (Annelida) from Japan: Unavailable Names Introduced by Uchida (2004) Revisited, with Reestablishment of their Availability
Fig. 3. Oxydromus bunbuku sp. nov., holotype (NSMT-Pol H-693) (B, E, F) and paratypes (the others). A, dorsal view of the anterior end, with proboscis not everted. B, the same, with proboscis everted. C, ventral view of the anterior end, with proboscis everted. D, dorsal view of the posterior end. E, anterior view of right parapodium 24. F, posterior view of the same parapodium. G, notoaciculae of left parapodium 32 (the same specimen as C). H, I, two (=all) compound falcigers of the long-blade type in supra-acicular region. J, K, compound falciger of the short-blade type in supra-acicular region, and its enlarged image. L, M, two (=all) falcigers of the long-blade type in sub-acicular region. N, falciger of the short-blade type in sub-acicular region. Scale bars: 1 mm for A, E; 1.5 mm for B–D; 0.5 mm for F; 0.05 mm for G, K; 0.1 mm for H–J, L–N.
Fig. 2 in New Hesionidae (Annelida) from Japan: Unavailable Names Introduced by Uchida (2004) Revisited, with Reestablishment of their Availability
Fig. 2. Oxydromus brevipodius sp. nov., holotype (NSMT-Pol H-692). A, dorsal view of the anterior body. B, anterior view of right parapodium 21 (with dorsal cirrus of short type). C, anterior view of right parapodium 22 (with dorsal cirrus of long type). D, posterior view of right parapodium 21. E, enlarged anterior view of notopodium of the same. F, notochaeta. G–I, supra-acicular neurochaetae: G, inferior; H, median; I, superior. J–L, sub-acicular neurochaetae: J, superior; K, median; L, inferior. Scale bars: 1 mm for A; 0.5 mm for B, C; 0.2 mm for D; 0.1 mm for E; 0.02 mm for F; 0.05 mm for G–L.
Figure 3 in Wild Relatives of the Eggplant (Solanum melongena L.: Solanaceae): New Understanding of Species Names in a Complex Group
Figure 3. Fruit shape and colour variation in cultivars of the common eggplant, Solanum melongena. Photograph taken by J. Prohens. doi:10.1371/journal.pone.0057039.g003
Figure 2. A in Wild Relatives of the Eggplant (Solanum melongena L.: Solanaceae): New Understanding of Species Names in a Complex Group
Figure 2. A sample of form and leaf variation in Solanum campylacanthum A.Rich. from across its morphological and geographical range showing the cline in leaf shape from south to north. A. Habit with narrow elliptic leaves. B. Habit with small leaves, small flowers, and dense curved prickles. C. Habit with ovate leaves and no prickles. D. Habit with large prickles and multiple fruits per infructescence. E. Habit with lobed leaves. F. Habit with cordate leaves. G. Short-stalked trichome from abaxial side of leaf. (Based on: A, Mott 11B, country; B, Gilfillan 6056, country; C, Torre 7145, Mozambique; D, Stewart E33, country; E, G, Friis et al. 8107, Ethiopia; F, Friis 8505, Ethiopia) Scale bar: A–F = 4 cm; G = 0.4 mm. Drawn by Lucy T. Smith. doi:10.1371/journal.pone.0057039.g002
Figure 1 in Wild Relatives of the Eggplant (Solanum melongena L.: Solanaceae): New Understanding of Species Names in a Complex Group
Figure 1. Representative flower and fruit morphology of eggplant and its wild relatives. A. Solanum campylacanthum inflorescences (Kenya - Vorontsova et al. 157); B. Solanum incanum immature fruit (Kenya – Vorontsova et al. 203); C. Solanum insanum fruit cross-section (China – Wang et al. 2047); D. Solanum insanum inflorescence with several hermaphrodite flowers (China – Wang et al. 2039); E. Solanum linnaeanum with yellow mature and mottled green immature fruit, note highly dissected leaves (Spain - Knapp IM-10096); F. Solanum melongena flower with duplicated parts (China – Wang et al. 2042). Photographs: A, B taken M.S. Vorontsova; C, D, E, F taken by S. Knapp. doi:10.1371/journal.pone.0057039.g001
Fig. 1 in Taxonomic studies on Malagasy Dalbergia (Fabaceae). II. A new name for D. mollis and the reinstatement of D. chermezonii
Fig. 1. – Variation in shape and size of leaflets. Dalbergia bemarivensis Phillipson & N. Wilding: A–D. Upper surface; E. Lower surface. Dalbergia chermezonii R. Vig.: F–I. Upper surface; J. Lower surface.
Fig. 2 in Taxonomic studies on Malagasy Dalbergia (Fabaceae). II. A new name for D. mollis and the reinstatement of D. chermezonii
Fig. 2. –Dalbergia bemarivensis Phillipson & N. Wilding: A. Young leafy fruiting branch; B. Leafy branch with mature fruit,
FIGURE 1 in Bozorgnites nom. nov. and Crassispirellina nom. nov.: New names for the preoccupied foraminiferal genera Bozorgniella and Crassispirella
FIGURE 1. Bozorgnites tumultuosus (Bozorgnia, 1973) modified from plate 12, figures 6-12 in Bozorgnia (1973). 1, paratype. Axial section. Immature specimen, similar to Eoparastaffellina but showing a subcarinate periphery in the inner whorls and chomata. 2, paratype. Typical axial section. 3, holotype. Axial section. Subcarinate periphery at the penultimate whorl, rounded in the other whorls. 4-7, four paratypes relatively similar to Eoparastaffellina, except for the strong chomata. Scale bar equals 0.300 mm.
FIGURE 2 in Bozorgnites nom. nov. and Crassispirellina nom. nov.: New names for the preoccupied foraminiferal genera Bozorgniella and Crassispirella
FIGURE 2. Crassispirellina hughesi (Gaillot and Vachard, 2007) modified from plate 55, figure 3; plate 56, figure 10; plate 59, figure 8; plate 66, figures 17-18; plate 69, figure 4 in Gaillot and Vachard (2007). 1, paratype relatively atypical (see comments in the text). 2, holotype. Axial section (see comments in the text). 3, paratype. Subequatorial section relatively well-preserved in the last whorls. 4-6, three paratypes in subaxial sections (see comments in the text for Figure 2.6). Scale bar equals 0.400 mm.
Figure 1. Part 1 in Temminck's new bird names introduced in the early parts of the Nouveau recueil de planches coloriées d'oiseaux in 1820-22
Figure 1. Part 1 front of wrapper of livraison 1 (apart from part number and date, the same for all 20 parts).
Figure 2. Part 2 in Temminck's new bird names introduced in the early parts of the Nouveau recueil de planches coloriées d'oiseaux in 1820-22
Figure 2. Part 2 back of wrapper of livraison 16 (showing list of included plates with scientific names and an important footnote).
Figure 7 in FLORA OF NEPAL NOTULAE IV: NEW SPECIES AND RESURRECTED NAMES IN SILENE
Figure 7. Silene nepalensis: A, whole plant; B, whole plant; C, lower stem node; D, calyx; E, teeth cilia; F, vein pubescence; G, calyx; H, upper part of pedicel; I, petal; J, petal; K, petal; L, seed. Silene poa Lidén, sp. nov.: M, whole plant; N, whole plant; O, calyx; P, teeth cilia; Q, vein pubescence; R, upper part of pedicel; S, calyx vein en face; T, seed; U, petal. Scale bars: A, B, M, N, 10 cm; C, D, G, I–K, O, U, 1 cm; E, F, H, L, P–T, 1 mm. Vouchers: A, K, H. Ohba et al. 8580491 (E); B, J, H. Ikeda et al. 20811234 (E); C–F, I, L, M. Wakabayashi et al. 9730195 (E); G, H, Durham univ. exp. D037 (KATH); M, Dep. Med. Pl. Kathmandu 6293 (KATH); N, S, U, PSW 2570 (E); O–R, T, J.F. Duthie 2742 (DD). Drawings: Magnus Lidén.
Figure 4 in FLORA OF NEPAL NOTULAE IV: NEW SPECIES AND RESURRECTED NAMES IN SILENE
Figure 4. Silene thomsonii: A, eastern form; B, 'weedy' lowland form; C, widespread form (except the extreme east of the distribution area). Photographs: A and B, E. Byers; C, K. Halberg.
Figure 3 in FLORA OF NEPAL NOTULAE IV: NEW SPECIES AND RESURRECTED NAMES IN SILENE
Figure 3. Silene thomsonii: A, whole plant, low-altitude form; B, whole plant, Central Nepalese form to which the type of the name S. thomsonii belongs; C, whole plant, Central Nepalese form to which the type of the name S. thomsonii belongs; D, whole plant, eastern form from Solukhumbu; E, calyx (drawn from resoftened herbarium material; the calyces are much more closed when fresh, see Figure 4); F, calyx (drawn from resoftened herbarium material; the calyces are much more closed when fresh, see Figure 4); G, hairs on calyx teeth; H, hairs on calyx veins; I, upper part of pedicel; J, seed; K, seed; L, petal; M, petal. Scale bars: A–D, 10 cm; E, F, L, M, 1 cm; G–K, 1 mm. Vouchers: A, Suzuki et al. 9485253 (E); B, Hoshino et al. 9666181 (E); C, Yon 165 (E); D, Wakabayashi et al. 9710312 (E); E, Suzuki et al. 9485253 (E); F–H, B. Yon 233 (E); I, DNEP3 AY36 (E); J, Wakabayashi et al. 9710312 (E); K, KR 9740430 (KATH); L, B. Yon 233 (E); M, DNEP3 AY36 (E). Drawings: Magnus Lidén.
Figure 2. A in FLORA OF NEPAL NOTULAE IV: NEW SPECIES AND RESURRECTED NAMES IN SILENE
Figure 2. A small plant of Silene scoparia in a rock wall between Lupra and Kagbeni. Note the infection by Microbotryum violaceum affecting the anthers. Photograph: Michelle Page.
Figure 1 in FLORA OF NEPAL NOTULAE IV: NEW SPECIES AND RESURRECTED NAMES IN SILENE
Figure 1. Silene scoparia Lidén, sp. nov.: A, whole plant leaf rosettes; B, whole plant with flowers (two damaged flowers have been 'mended' for clarity, with the mended parts appearing lighter); C, calyx (insert: calyx teeth); D, hairs on calyx veins; E, hairs on pedicels; F, hairs on calyx teeth vein; G, petal; H, cauline leaf; I, seed. Silene oreoploca Lidén, nom. nov.: J, whole plant with flowers; K, calyx (insert: calyx teeth); L, hairs on calyx veins; M, hairs on pedicels; N, petal; O, cauline leaf; P, seed; Q, androgynophore pubescence. Silene moorcroftiana Wall. ex Benth.: R, whole plant with flowers; S, calyx (insert: calyx teeth); T, hairs on calyx veins; U, hairs on pedicels; V, petal; W, cauline leaf; X, seed; Y, androgynophore pubescence. Scale bars: A, B, J, R, 10 cm; G, H, N, O, V, W and C, K, S (excluding inserts), 1 cm; C, K, S (inserts), 2 mm; D–F, I, L, P, Q, T, X and Y, 1 mm. Vouchers: A, Y. Iokawa et al. 20020015 (E00826586); B, M. Minaki et al. 9104467 (E00231757); C–I, G. Miehe, S. Miehe & K. Koch 01-076-08 (GB); J, Tibet herbal medicine census 1666 (PE); K–O, Chen Jia-Rui 92294 (PE); P and Q, Miehe 99-49-10 (GB); R, S. Noshiro et al. 20106115 (TI); S–Y, S. Miehe 99-62-16 (GB). Drawings: Magnus Lidén.
Figure 5 in FLORA OF NEPAL NOTULAE IV: NEW SPECIES AND RESURRECTED NAMES IN SILENE
Figure 5. Silene nyalamensis (L.H.Zhou) Lidén, comb. nov.: A, calyx; B, petal; C, seed; D, whole plant; E, upper part of pedicel; F, calyx vein pubescence; G, calyx teeth cilia. Silene blepharicalyx Lidén, sp. nov.: H, calyx; I, petal; J, seed; K, whole plant; L, upper part of pedicel; M, calyx vein pubescence; N, calyx teeth cilia. Silene procera Lidén, sp. nov.: O, calyx; P, petal; Q, seed; R, S, whole plant; T, upper part of pedicel; U, calyx vein pubescence; V, calyx teeth cilia. Scale bars: A, B, H, I, O, P, 1 cm; C, E–G, J, L–N, Q, T–V, 1 mm; D, K, R, S, 10 cm. Vouchers: A, C–G, Tibet herbal medicine census 1832 (PE); B, Banerji & P.R. Shakya 5706 (KATH); H, L–N, K.K. Shrestha & S.K. Ghimire SP363 (KATH); I, J, S. Noshiro et al. 20106081 (E); K, A. Stainton, W.R. Sykes & L.H.J. Williams 2197 (E); O, P, R–V, H. Ikeda et al. (Manaslu 2008 expedition) 20815090 (E); Q, H. Ikeda et al. 20811114 (E). Drawings: Magnus Lidén.
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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.