Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
5,200
datasets available to search
ShareScore release 0.9.0
Dataset results
5,200 results for “northern species”
Рис. 1. Parasphaerolaimus tropicus sp. nov., самец. А — общий виΑ; Б — переΑний конец теΛа; В — заΑний конец теΛа. Масштаб: А — 150 мкм; Б, В — 50 мкм Fig. 1. Parasphaerolaimus tropicus sp. nov., male. А — general view; Б — anterior body end; В — posterior body end. Scale bars: А — 150 μm; Б, В — 50 μm in Two New Species Of The Genus Ditlevsen, 1918 (Nematoda, Monhysterida) From Water Bodies Of Northern Vietnam
Рис. 1. Parasphaerolaimus tropicus sp. nov., самец. А — общий виΑ; Б — переΑний конец теΛа; В — заΑний конец теΛа. Масштаб: А — 150 мкм; Б, В — 50 мкм Fig. 1. Parasphaerolaimus tropicus sp. nov., male. А — general view; Б — anterior body end; В — posterior body end. Scale bars: А — 150 μm; Б, В — 50 μm
Data and Code from: Wildfire influences species assemblage and habitat utilisation of boreal wildlife after more than a decade in northern Sweden
<p>Data and Code supporting the analyses presented in: Fredriksson, Cromsigt & Hofmeester - Wildfire influences species assemblage and habitat utilisation of boreal wildlife after more than a decade in northern Sweden as published in Wildlife Biology</p> <p><strong>Abstract</strong></p> <p><span>Fires can strongly change the vegetation structure and the availability of resources for wildlife, but fire suppression has long affected the natural role of fire in shaping boreal ecosystems in northern Europe. Recently, wildfires have increased in frequency, possibly due to global warming. In contrast to the boreal systems in North America, there have been few studies on responses of wildlife to wildfires in northern Europe. Based on the findings from North America, we predict that responses of wildlife to wildfire vary among wildlife species: where mammalian herbivores, such as moose (<em>Alces alces</em>) and mountain hare (<em>Lepus timidus</em>), will be attracted to burnt areas following an increase in food availability, other species, such as reindeer (<em>Rangifer tarandus</em>), are negatively impacted due to fire reducing their preferred food. We then tested our predictions by contrasting wildlife utilization of sites that burnt by wildfire in 2006 with nearby unburnt control sites in three areas in northern Sweden. To measure wildlife utilization, we used 72 camera traps, equally divided between the burnt and control sites, with two placement strategies: random and on wildlife trails. The cameras recorded 27 mammal and bird species during summer 2018. Species assemblage differed between burnt and control sites. Fieldfare (<em>Turdus pilaris</em>) used burnt sites more than control sites, while pine marten (<em>Martes martes</em>) and western capercaillie (<em>Tetrao urogallus</em>) used control sites more than burnt sites. We however did not find support for a positive effect of past forest fires on any of the observed wild mammals. We discuss how, due to the impact of forestry, forage-rich habitat may not be as limiting in Scandinavia as in the North-American context, potentially leading to recently burnt sites being less attractive to herbivores such as moose.</span></p>
Fig. 1 in The effects of short-term climate change on the range of species: the case of the expanding European dwarf mantis Ameles spallanzania in northern Italy (Mantodea: Amelidae)
Fig. 1 – Distribution of Ameles spallanzania in Italy across a, past period and b, current period. Confirmed data refer to already known presence cells in the previous time interval.
Figures 31–37 in Two new species of Hottentotta Birula, 1908 (Scorpiones: Buthidae) from northern Oman
Figures 31–37: H. saxinatans, sp. nov., holotype male. 31. Carapace and tergites I–II, dorsal aspect. 32–33, right chelicera. 32. Dorsal aspect. 33. Ventral aspect. 34–35, right basitarsus and telotarsus III. 34. Ventral aspect. 35. Retrolateral aspect. 36–37, metasoma and telson. 36. Right lateral aspect. 37. Ventral aspect. Scale bar: 31: 2.75 mm; 32–33: 2 mm; 34–35: 1.3 mm; 36–37: 5.5 mm.
Figures 12–20 in Two new species of Hottentotta Birula, 1908 (Scorpiones: Buthidae) from northern Oman
Figures 12–20: H. pellucidus, sp.nov., 12–16, 19, holotype male; 17–18, paratype male; 20, paratype female. 12. Right pedipalp femur, dorsal aspect. 13. Right pedipalp patella, dorsal aspect. 14. Right pedipalp patella, external aspect. 15. Right pedipalp chela, external aspect. 16. Right pedipalp chela, ventral aspect. 17–18. Right hemispermatophore, lobes at base of flagellum. 17. Convex aspect. 18. Inner aspect. 19. Left male pectine, ventral aspect. 20. Left female pectine ventral aspect. Scale bar: 12–16, 19–20: 4.1 mm; 17–18: 1.06 mm.
Figures 5–11 in Two new species of Hottentotta Birula, 1908 (Scorpiones: Buthidae) from northern Oman
Figures 5–11: H. pellucidus, sp. nov. 5, 8–11, holotype male; 6–7, paratype male (Jabal Bani Jabir). 5. Carapace and tergites I– II, dorsal aspect. 6–7, right chelicera. 6. Dorsal aspect. 7. Ventral aspect. 8–9, right basitarsus and telotarsus III. 8. Ventral aspect. 9. Retrolateral aspect. 10–11, metasoma and telson. 10. Right lateral aspect. 11. Ventral aspect. Scale bar: 5: 3.19 mm; 6–7: 2.125 mm; 8–9: 1.5 mm; 10–11: 6.22 mm.
Figures 38–46 in Two new species of Hottentotta Birula, 1908 (Scorpiones: Buthidae) from northern Oman
Figures 38–46: H. saxinatans, sp. nov., 38–45, holotype male; 46, paratype female. 38. Right pedipalp femur, dorsal aspect. 39. Right pedipalp patella, dorsal aspect. 40. Right pedipalp patella, external aspect. 41. Right pedipalp chela, external aspect. 42. Right pedipalp chela, ventral aspect. 43–44. Right hemispermatophore, lobes at base of flagellum. 43. Convex aspect. 44. Inner aspect. 45. Left male pectine, ventral aspect. 46. Left female pectine ventral aspect. Scale bar: 38–42, 45–46: 2 mm; 43–44: 0.68 mm.
Figures 27–30 in Two new species of Hottentotta Birula, 1908 (Scorpiones: Buthidae) from northern Oman
Figures 27–30: H. saxinatans, sp. nov., habitus, 27–28, holotype male; 29–30, paratype female. 27, 29. Dorsal aspect. 28, 30. Ventral aspect. Scale bar: 10 mm.
Figure 64 in A new species of Odontobuthus (Scorpiones: Buthidae) from northern Oman
Figure 64: Plot of collection sites of Odontobuthus brevidigitus sp. nov., (magenta circles) in northern Oman.
Figures 1–4 in Two new species of Hottentotta Birula, 1908 (Scorpiones: Buthidae) from northern Oman
Figures 1–4: H. pellucidus, sp. nov., habitus, 1–2, holotype male; 3–4, paratype female. 1, 3. Dorsal aspect. 2, 4. Ventral aspect. Scale bar: 10 mm.
Figures 60–63 in A new species of Odontobuthus (Scorpiones: Buthidae) from northern Oman
Figures 60–63: Scatter plots showing variation in selected meristic and morphometric data from Odontobuthus, comparing the new species to other members of the genus. 60. Plot of primary denticle counts (excluding proximal subrow) of pedipalp chela fixed finger vs. movable finger. 61. Plot of pectine basal middle lamella length/ width vs. pectine length/ carapace length, for females. 62. Plot of Pedipalp chela movable finger length/ chela manus ventral length for males. 63. Plot of Pedipalp chela movable finger length/ chela manus ventral length for females. Color key for all plots is shown in legend of Fig. 60: magenta circles, O. brevidigitus sp. nov.; red circles, O. bidentatus; yellow circles, O. doriae; green circles, O. odonturus.
Figure 65 in A new species of Odontobuthus (Scorpiones: Buthidae) from northern Oman
Figure 65: Plot of collection sites of all four species of Odontobuthus on a topographic map of the Middle East. Magenta circles, O. brevidigitus sp. nov.; red circles, O. bidentatus Lourenço et Pézier, 2002; yellow circles, O. doriae (Thorell, 1876); green circles, O. odonturus (Pocock, 1897); open circles, O. sp. (indeterminate) (locality data from specimens examined and literature records: Birula, 1900, 1905; Kovařík, 1997; Lourenço & Pézier, 2002; Navidpour et al., 2008a, 2008b, 2008c, 2008d; Pirali-Kheirabadi et al., 2008).
Figures 56–59 in A new species of Odontobuthus (Scorpiones: Buthidae) from northern Oman
Figures 56–59: Ventral aspect of metasoma V. 56–57, Odontobuthus brevidigitus sp. nov. 56. Holotype male. 57. Paratype female. 58–59, O. bidentatus. 58. Male (Omidiyeh). 59. Female (Ahram). Scale bar: 56: 2.00 mm; 57: 2.17 mm; 58: 2.90 mm; 59: 2.40 mm. Photographed under UV fluorescence.
Figures 45–48 in A new species of Odontobuthus (Scorpiones: Buthidae) from northern Oman
Figures 45–48: Odontobuthus bidentatus, habitus under UV fluorescence. 45–46, male (Omidiyeh). 45. Dorsal aspect. 46. Ventral aspect. 47–48, female (Ahram). 47. Dorsal aspect. 48. Ventral aspect. Scale bar: 20 mm.
Figures 37–44 in A new species of Odontobuthus (Scorpiones: Buthidae) from northern Oman
Figures 37–44: Representative basal lamellae of the pectines of Odontobuthus species. 37, 38. O. brevidigitus sp. nov.; 37, holotype male; 38, paratype female (from type locality). 39, 40. O. doriae (Tabiz, Iran); 39, male; 40, female. 41, 42. O. odonturus; 41, male (Lalian, Pakistan); 42, female (Manshera, Pakistan). 43, 44. O. bidentatus; 43, male (Omidiyeh); 44, female (Ahram).
Figures 25–30 in A new species of Odontobuthus (Scorpiones: Buthidae) from northern Oman
Figures 25–30: Trichobothrial map of the pedipalp of Odontobuthus brevidigitus, sp. nov. 25–28, holotype male; 29–30, paratype male (Seeb). 25. Base of femur, internal aspect. 26. Femur, dorsal aspect. 27. Patella, dorsal aspect. 28. Patella, external aspect. 29. Chela, external aspect. 30. Chela, ventral aspect. Trichobothrial notation after Vachon (1974). Trichobothria on exposed surfaces indicated by solid circles, those on hidden surfaces indicated by dotted circles.
Figures 31–36 in A new species of Odontobuthus (Scorpiones: Buthidae) from northern Oman
Figures 31–36: Lateral views of metasoma II–III, V and telson of Odontobuthus species, showing carinal dentition. 31–32, O. bidentatus (Omidiyeh, Iran); 33–34, O. odonturus (Lalian, Pakistan); 35–36, O. doriae (Tabiz, Iran). 31, 33, 35. Metasoma II–III, lateral aspect. 32, 34, 36. Metasoma V and telson, lateral aspect. Scale bar: 31–32: 5 mm; 33–34: 3.27 mm; 35–36: 4.30 mm.
Figures 16–24 in A new species of Odontobuthus (Scorpiones: Buthidae) from northern Oman
Figures 16–24: Odontobuthus brevidigitus, sp. nov. 16–18, 21, 23–24, holotype male; 19–20, paratype male (Ghubrah); 22, topoparatype female. 16. Right pedipalp femur, dorsal aspect. 17. Right pedipalp patella, dorsal aspect. 18. Right pedipalp patella, external aspect. 19. Right pedipalp chela, external aspect. 20. Right pedipalp chela, ventral aspect. 21. Left pectine, male, ventral aspect. 22. Left pectine, female, ventral aspect. 23. Right basitarsus and telotarsus III, retrolateral aspect. 24. Right telotarsus III, ventral aspect. Scale bar: 16–20: 4.00 mm; 21–22: 5.36 mm; 23: 3.00 mm; 24: 2.00 mm.
Figures 21–26 in Two new species of Hottentotta Birula, 1908 (Scorpiones: Buthidae) from northern Oman
Figures 21–26: H. pellucidus, sp. nov., trichobothrial map, holotype male. 21. Right pedipalp femur, dorsal aspect. 22. Right pedipalp femur, proximal internal aspect. 23. Right pedipalp patella, dorsal aspect. 24. Right pedipalp patella, external aspect. 25. Right pedipalp chela, external aspect. 26. Right pedipalp chela, ventral aspect. Trichobothrial notation after Vachon (1974).
Figures 65–66 in Two new species of Hottentotta Birula, 1908 (Scorpiones: Buthidae) from northern Oman
Figures 65–66: Maps showing collection sites of new species of Hottentotta in northern Oman. 65. Records plotted on larger scale terrain and elevation map of southeast Arabia with geopolitical borders. 66. Records plotted on color topographic map of northern Oman showing locations in the Al Hajar mountain ranges. Magenta circles: H. pellucidus, sp. nov.; red circles: H. saxinatans, sp. nov. The isolated record of H. pellucidus at Muscat may be spurious.
ScienceDex guides
Understand access before you commit
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.