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Figures 5–7 in Two new species of hydromedusa (Cnidaria) from the Leizhou Bay, the northern South China Sea
Figures 5–7. Octocannoides tetranema Xu, Guo & Wang, sp. nov. 5–6. Oval views. 7. Lateral view. Scale bars = 0.5 mm.
Figure 5 in A New Species of Caprella (Crustacea: Amphipoda: Caprellidae) from Gippsland Lakes, Australia, with a Redescription of Caprella acanthogaster Mayer, 1890 from Northern Japan
Figure 5. Caprella tamboensis sp. nov. from Tambo Bay, Lake King, Gippsland Lakes, Victoria, Australia. Holotype, male, AM P.102618, 21.93 mm. Paratype, female, AM P.102620, 9.40 mm. Bar indicates 1.0 mm.
Figure 6 in A New Species of Caprella (Crustacea: Amphipoda: Caprellidae) from Gippsland Lakes, Australia, with a Redescription of Caprella acanthogaster Mayer, 1890 from Northern Japan
Figure 6. Caprella tamboensis sp. nov. from Tambo Bay, Lake King, Gippsland Lakes, Victoria, Australia. Holotype, male, AM P.102618, 21.93 mm. Bar indicates 1.0 mm, except for 0.1 mm to AB.
Figure 4 in A New Species of Caprella (Crustacea: Amphipoda: Caprellidae) from Gippsland Lakes, Australia, with a Redescription of Caprella acanthogaster Mayer, 1890 from Northern Japan
Figure 4. Distribution of Caprella acanthogaster Mayer, 1890 and related species. Data is based on Mayer (1890), Schruin (1937), Utinomi (1943a,b), Arimoto (1976), Vassilenko (1974), Wang et al. (1989), Lee & Lee (1993), Hosono & Munehara (2001), Guerra-García & Takeuchi (2004), Takeuchi (2005), Lee & Hong (2009, 2011), Cao et al. (2013), Wei et al. (2016), Heo et al. (2020), and the present study.
Figure 8 in A New Species of Caprella (Crustacea: Amphipoda: Caprellidae) from Gippsland Lakes, Australia, with a Redescription of Caprella acanthogaster Mayer, 1890 from Northern Japan
Figure 8. Aggregation of Caprella tamboensis sp. nov. on a fishing net in Tambo Bay, Lake King, Gippsland Lakes, Victoria, Australia. The image was taken from a screen shot of the video recorded by Mr M. Jenkins when the specimens reported here were collected.
Figure 3. Caprella acanthogaster Mayer, 1890 in A New Species of Caprella (Crustacea: Amphipoda: Caprellidae) from Gippsland Lakes, Australia, with a Redescription of Caprella acanthogaster Mayer, 1890 from Northern Japan
Figure 3. Caprella acanthogaster Mayer, 1890 from Otsuchi Bay, Iwate, Japan. Male, AM P.105618, 38.06 mm. Bar indicates 0.1 mm.
Figure 7 in A New Species of Caprella (Crustacea: Amphipoda: Caprellidae) from Gippsland Lakes, Australia, with a Redescription of Caprella acanthogaster Mayer, 1890 from Northern Japan
Figure 7. Caprella tamboensis sp. nov. from Tambo Bay, Lake King, Gippsland Lakes, Victoria, Australia. Holotype, male, AM P.102618, 21.93 mm. Bar indicates 0.1 mm.
Figure 2. Caprella acanthogaster Mayer, 1890 in A New Species of Caprella (Crustacea: Amphipoda: Caprellidae) from Gippsland Lakes, Australia, with a Redescription of Caprella acanthogaster Mayer, 1890 from Northern Japan
Figure 2. Caprella acanthogaster Mayer, 1890 from Otsuchi Bay, Iwate, Japan. Male, AM P.105618, 38.06 mm. Bar indicates 1.0 mm, except for 0.1 mm to AB.
Figure 1. Caprella acanthogaster Mayer, 1890 in A New Species of Caprella (Crustacea: Amphipoda: Caprellidae) from Gippsland Lakes, Australia, with a Redescription of Caprella acanthogaster Mayer, 1890 from Northern Japan
Figure 1. Caprella acanthogaster Mayer, 1890 from Otsuchi Bay, Iwate, Japan. Male, AM P.105618, 38.06 mm. Female, AM P.105619, 12.37 mm. Bar indicates 1.0 mm.
Fig. 4 in Taxonomic studies on Malagasy Dalbergia (Fabaceae). I. Two new species from northern Madagascar, and an emended description for D. manongarivensis
Fig. 4. – Dalbergia manongarivensis Bosser & R. Rabev. A. Flowering branch; B. Fruiting branch; C. Young inflorescence; D. Flower; E. Fruit;
Fig. 3 in Taxonomic studies on Malagasy Dalbergia (Fabaceae). I. Two new species from northern Madagascar, and an emended description for D. manongarivensis
Fig. 3. – Dalbergia antsirananae Phillipson, Crameri & N. Wilding. A. Flowering branch; B. Fruiting branch; C. Part of young inflorescence; D. Leaflet (lower surface); E. Flower; F. Fruit; G: Calyx (split open and flattened) inner surface (left) and outer surface (right); H. Standard petal (adaxial surface); I. Wing petal (adaxial surface); J. Keel petal (adaxial surface); K. Androecium (split open to show
Fig. 2 in Taxonomic studies on Malagasy Dalbergia (Fabaceae). I. Two new species from northern Madagascar, and an emended description for D. manongarivensis
Fig. 2. – Dalbergia antsirananae Phillipson, Crameri & N. Wilding. A. Flowering branch; B. Fruiting branch; C: Leafy branch from coppice shoot, showing underside of leaves with distinctive pale brown indument on the laminae, contrasting with leaves on fertile branches; D: Bole of large felled tree (foreground) and large standing tree (background).
Figs. 15–18 in Two new water mite species of the genus Lebertia Neuman, 1880 (Acari, Hydrachnidae: Lebertiidae) from northern lakes of Russia
Figs. 15–18. Lebertia prokini sp. n., male: 15 — genital field, right side; 16 — chelicera; 17 — IV-Leg-6; 18 — leg claw. Lebertia porosa, male: 19 — fragment of integument; 20 — pedipalp. Scale bars: 15–17 = 100 μm, 18 = 50 μm Рис. 15–18. Lebertia prokini sp. n., самец: 15 — генитаΛьное поΛе, правая сторона; 16 — хеΛицера; 17 — Λапка ноги IV; 18 — коготок ног. Lebertia porosa, самец: 19 — фрагмент покрова; 20 — пеΔипаΛьпа. ШкаΛы: 15–17 = 100 μm, 18 = 50 μm
Figs. 10–14 in Two new water mite species of the genus Lebertia Neuman, 1880 (Acari, Hydrachnidae: Lebertiidae) from northern lakes of Russia
Figs. 10–14. Lebertia prokini sp. n., male: 10 — seta Fch; 11 — seta Oi; 12 — seta Oe; 13 — ventral view; 14 — pedipalp, lateral view. Scale bars: 10– 13 = 100 μm; 14 = 50 μm Рис. 10-14. Lebertia prokini sp. n., самец: 10 — щетинка Fch; 11 — щетинка Oi; 12 — щетинка Oe; 13 — вентраΛьная сторона; 14 — пеΔипаΛьпа, боковая сторона. ШкаΛы: 10–13 = 100 μm; 14 = 50 μm
Figs. 1–5 in Two new water mite species of the genus Lebertia Neuman, 1880 (Acari, Hydrachnidae: Lebertiidae) from northern lakes of Russia
Figs. 1–5. Lebertia makarovae sp. n., female: 1 — seta Fch; 2 — seta Oi; 3 — seta Oe; 4 — ventral view; 5 — pedipalp. Scale bars: 1–3, 5 = 100 μm; 4 = 200 μm Рис. 1–5. Lebertia makarovae sp. n., самка: 1 — щетинка Fch; 2 — щетинка Oi; 3 — щетинка Oe; 4 — вентраΛьная сторона; 5 — пеΔипаΛьпа. ШкаΛы: 1–3, 5 = 100 μm; 4 = 200 μm
Рис. 2. Распредение биомассы Mytilus trossulus septentrionalis на литорали дальневоcточных морей России. Здесь и далее на гистограммах по оси абцисс после географических пунктов в скобках укаЗана выборка (число иЗученных проб), по оси ординат – максимальные ЗначениЯ биомассы вида. Под Значением биомассы 0.1 г/м² подраЗумеваютсЯ качественные пробы. СокраЩениЯ (бмп) и (топ) оЗначают соответственно беринговоморское и тихоокеанское побережьЯ Восточной Камчатки. Побережье Зал. Петра Великого от устьЯ р. Туманной к северу до м. Поворотного условно отноcитсЯ к южному Приморью; побережье к северу от м. Поворотного (пос. Преображение, б. СоколовскаЯ) до б. Ольга, включительно, условно относитсЯ к среднему Приморью; побережье к северу от б. Ольга до м. Белкина и материковое побережье Татарского пролива относим к северному Приморью. Fig. 2. The distribution of biomass of Mytilus trossulus septentrionalis in the intertidal zone of the Far Eastern seas of Russia. Here and throughout on histograms, on the abcissa is the number of studied samples (numbers in parentheses following the names geographic localities), on the ordinate is the maximum biomass of species. The number 0.1 g wet wt m-2 means the qualitative samples. Abbreviations (bmp) and (top) mean the Bering Sea coast and the Pacific coast of eastern Kamchatka. The coast of Peter the Great Bay from the mouth of the Tumannaya River to Cape Povorotny is conditionally referred to as southern Primorye; the area north of Cape Povorotny (Preobrazhenie Settlement, Sokolovskaya Bay) to Olga Bay inclusive is conditionally referred to as middle Primorye; north of Olga Bay to Cape Belkin and the mainland coast of the Tatar Strait to as northern Primorye. in Bivalve mollusks of the intertidal zone of the Far Eastern seas of Russia
Рис. 2. Распредение биомассы Mytilus trossulus septentrionalis на литорали дальневоcточных морей России. Здесь и далее на гистограммах по оси абцисс после географических пунктов в скобках укаЗана выборка (число иЗученных проб), по оси ординат – максимальные ЗначениЯ биомассы вида. Под Значением биомассы 0.1 г/м² подраЗумеваютсЯ качественные пробы. СокраЩениЯ (бмп) и (топ) оЗначают соответственно беринговоморское и тихоокеанское побережьЯ Восточной Камчатки. Побережье Зал. Петра Великого от устьЯ р. Туманной к северу до м. Поворотного условно отноcитсЯ к южному Приморью; побережье к северу от м. Поворотного (пос. Преображение, б. СоколовскаЯ) до б. Ольга, включительно, условно относитсЯ к среднему Приморью; побережье к северу от б. Ольга до м. Белкина и материковое побережье Татарского пролива относим к северному Приморью. Fig. 2. The distribution of biomass of Mytilus trossulus septentrionalis in the intertidal zone of the Far Eastern seas of Russia. Here and throughout on histograms, on the abcissa is the number of studied samples (numbers in parentheses following the names geographic localities), on the ordinate is the maximum biomass of species. The number 0.1 g wet wt m-2 means the qualitative samples. Abbreviations (bmp) and (top) mean the Bering Sea coast and the Pacific coast of eastern Kamchatka. The coast of Peter the Great Bay from the mouth of the Tumannaya River to Cape Povorotny is conditionally referred to as southern Primorye; the area north of Cape Povorotny (Preobrazhenie Settlement, Sokolovskaya Bay) to Olga Bay inclusive is conditionally referred to as middle Primorye; north of Olga Bay to Cape Belkin and the mainland coast of the Tatar Strait to as northern Primorye.
Рис. 2. A, B. Modiolus (Modiolus) kurilensis Bernard, 1983: леваЯ створка снаружи (A), иЗнутри (B). Длина раковины 26.4 мм, высота – 47.3 мм; C, D. Gari (Gobraeus) kazusensis (Yokoyama, 1922): леваЯ створка снаружи (C), иЗнутри (D). Длина раковины 71.0 мм, высота – 39.9 мм. E, F. Panomya norvegica (Spengler, 1973): леваЯ створка снаружи (E), праваЯ створка иЗнутри (F). Длина раковины 70.8 мм, высота – 44.5 мм, толЩина – 36.7 мм. Fig. 2. A, B. Modiolus (Modiolus) kurilensis Bernard, 1983: left valve (A) outside, (B) inside. Shell length 26.4 mm, height – 47.3 mm. C, D. Gari (Gobraeus) kazusensis (Yokoyama, 1922): left valve (C) outside, (D) inside. Shell length 71.0 mm, height – 39.9 mm. E, F. Panomya norvegica (Spengler, 1973): left valve (E) outside, right valve (F) inside. Shell length 70.8 mm, height – 44.5 mm, thickness – 36.7 mm. in On the species composition of marine bivalves of the Sikhote-Alin Reserve (northern Primorye, Japan/East Sea)
Рис. 2. A, B. Modiolus (Modiolus) kurilensis Bernard, 1983: леваЯ створка снаружи (A), иЗнутри (B). Длина раковины 26.4 мм, высота – 47.3 мм; C, D. Gari (Gobraeus) kazusensis (Yokoyama, 1922): леваЯ створка снаружи (C), иЗнутри (D). Длина раковины 71.0 мм, высота – 39.9 мм. E, F. Panomya norvegica (Spengler, 1973): леваЯ створка снаружи (E), праваЯ створка иЗнутри (F). Длина раковины 70.8 мм, высота – 44.5 мм, толЩина – 36.7 мм. Fig. 2. A, B. Modiolus (Modiolus) kurilensis Bernard, 1983: left valve (A) outside, (B) inside. Shell length 26.4 mm, height – 47.3 mm. C, D. Gari (Gobraeus) kazusensis (Yokoyama, 1922): left valve (C) outside, (D) inside. Shell length 71.0 mm, height – 39.9 mm. E, F. Panomya norvegica (Spengler, 1973): left valve (E) outside, right valve (F) inside. Shell length 70.8 mm, height – 44.5 mm, thickness – 36.7 mm.
FIGURE 4 in A new striped species of Brachychalcinus (Ostariophysi: Characiformes) from Amapá and Pará states, northern Brazil
FIGURE 4 | Brachychalcinus species groups according to color pattern: 1. "B. copei pattern": A. B. copei, LBP 23616, 81.3 mm SL; B. B. restrospina, NUP 21577, 58.7 mm SL; C. B. nummus, LBP 28578, 48.0 mm SL; D. B. parnaibae, MZUSP 87486, 54.1 mm SL. 2. "B. signatus pattern": E. B. orbicularis, ROM 102235, 52.1 mm SL; F. B. signatus, paratype, INPA 5667, 48.4 mm SL. 3. "B. reisi pattern": G. B. reisi, LBP 24499, 54.6 mm SL; H. B. sabaji, paratype, IEPA 4980, 62.8 mm SL, lateral view, left side. Scale bar = 1 mm.
FIGURE 5 in A new striped species of Brachychalcinus (Ostariophysi: Characiformes) from Amapá and Pará states, northern Brazil
FIGURE 5 | Preanal spine of Brachychalcinus: A. B. sabaji, LBP 34043, paratype, 52.6 mm SL; B. MCP 11033, B. orbicularis, 48.2 mm SL; C. B. reisi, paratype, MZUSP 119482, 52.2 mm SL, lateral view, left side. Scale bars = 1 mm.
FIGURE 3 in A new striped species of Brachychalcinus (Ostariophysi: Characiformes) from Amapá and Pará states, northern Brazil
FIGURE 3 | Map showing the known distribution of Brachychalcinus sabaji. Red star indicates the typelocality. Symbols may represent more than one lot.
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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.