Skip to main content
Powered by ShareScore

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.

46

datasets available to search

ShareScore release 0.9.0

Reset

Dataset results

46 results for “Pearson”

Learn how ShareScore rates datasets ↗
zenodo40/100

Phenological Trends in the California poppy (Pearson et al.): Dataset and analyses scripts

<p>These files contain the cleaned dataset of&nbsp;<em>Eschscholzia californica</em>&nbsp;herbarium specimen records and the R scripts used to analyze the data for Pearson et al. &quot;Phenological trends in the California poppy (<em>Eschscholzia californica</em>): Digitized herbarium specimens reveal intraspecific variation in the sensitivity of flowering date to climate change.&quot;</p>

opencc-by-4.0Dec 2019View details →
dryad36/100

Pearson correlation tests for environmental variables, Student t-test for range shift and comparisons for habitat loss in 2070

<p><span>Habitat loss and shifts associated with climate change threaten global biodiversity, with impacts likely to be most pronounced at high latitudes. With the disappearance of the tundra breeding habitats, migratory shorebirds that breed at these high latitudes are likely to be even more vulnerable to climate change than those in temperate regions. We examined this idea using new distributional information on two subspecies of Black-tailed Godwits <em>Limosa limosa</em> in Asia: the northerly, bog-breeding <em>L. l. bohaii</em> and the more southerly, steppe-breeding <em>L. l. melanuroides</em>. Based on breeding locations of tagged and molecularly assayed birds, we modelled the current breeding distributions of the two subspecies with species distribution models, tested those models for robustness, and then used them to predict climatically suitable breeding ranges in 2070 according to bioclimatic variables and different climate change scenarios. Our models were robust and showed that climate change is expected to push bohaii into the northern rim of the Eurasian continent. <em>Melanuroides</em> is also expected to shift northward, stopping in the Yablonovyy and </span><span>Stanovoy Ranges</span><span>, and breeding elevation is expected to increase.</span> <span>Climatically suitable breeding habitat ranges would shrink to 16% and 11% of the currently estimated ranges of <em>bohaii</em> and <em>melanuroides</em>, respectively. Overall, this study provides the first predictions for the future distributions of two little-known Black-tailed Godwit subspecies and highlights the importance of factoring in shifts in bird distribution when designing climate-proof conservation strategies.</span></p>

opencc-zeroJun 2022View details →
dryad36/100

Pearson correlation tests for environmental variables, Student t-test for range shift and comparisons for habitat loss in 2070

Open the record for dataset details and reuse information.

publicJun 2022View details →
zenodo32/100

On following pages: 94. Thomas's Horseshoe Bat (Rhinolophus thomasi); 95. Lesser Horseshoe Bat (Rhinolophus hipposideros); 96. rancis's Woolly Horseshoe Bat (Rhinolophus trancisi); 97. Lesser Woolly Horseshoe Bat (Rhinolophus sedulus); 98. Trefoil Horseshoe Bat (Rhinolophus trifoliatus); 99. Northern Woolly Horseshoe Bat (Rhinolophus perniger); 100. Selangor Woolly Horseshoe Bat (Rhinolophus luctoides); 101. Malaysian Woolly Horseshoe Bat (Rhinolophus mono); 102. Great Woolly Horseshoe Bat (Rhinolophus luctus); 1.03. Beddome's Woolly Horseshoe Bat (Rhinolophus beddomei); 104. Formosan Woolly Horseshoe Bat (Rhinolophus formosaë); 105. Thailand Horseshoe Bat (Rhinolophus thailandensis); 106. Dobson's Horseshoe Bat (Rhinolophus yunanensis); 107. Chiew Kwee's Horseshoe Bat (Rhinolophus chiewkweeae); 108. Pearson's Horseshoe Bat (Rhinolophus pearsonii); 109. Mitred Horseshoe Bat (Rhinolophus mitratus). in Rhinolophidae

On following pages: 94. Thomas's Horseshoe Bat (Rhinolophus thomasi); 95. Lesser Horseshoe Bat (Rhinolophus hipposideros); 96. rancis's Woolly Horseshoe Bat (Rhinolophus trancisi); 97. Lesser Woolly Horseshoe Bat (Rhinolophus sedulus); 98. Trefoil Horseshoe Bat (Rhinolophus trifoliatus); 99. Northern Woolly Horseshoe Bat (Rhinolophus perniger); 100. Selangor Woolly Horseshoe Bat (Rhinolophus luctoides); 101. Malaysian Woolly Horseshoe Bat (Rhinolophus mono); 102. Great Woolly Horseshoe Bat (Rhinolophus luctus); 1.03. Beddome's Woolly Horseshoe Bat (Rhinolophus beddomei); 104. Formosan Woolly Horseshoe Bat (Rhinolophus formosaë); 105. Thailand Horseshoe Bat (Rhinolophus thailandensis); 106. Dobson's Horseshoe Bat (Rhinolophus yunanensis); 107. Chiew Kwee's Horseshoe Bat (Rhinolophus chiewkweeae); 108. Pearson's Horseshoe Bat (Rhinolophus pearsonii); 109. Mitred Horseshoe Bat (Rhinolophus mitratus).

opennotspecifiedOct 2019View details →
zenodo32/100

Distribution. Known with certainty only from Chiang Mai Province, NW Thailand, although it is probably the species that occurs in NW, W & SE Thailand, including Tarutao I; specimens from Cambodia, found to be intermediate in size between Dobson's Horseshoe Bat (. yunanensis) and Pearson's Horseshoe Bat (. pearsonii), are also tentatively included in this species. in Rhinolophidae

Distribution. Known with certainty only from Chiang Mai Province, NW Thailand, although it is probably the species that occurs in NW, W &amp; SE Thailand, including Tarutao I; specimens from Cambodia, found to be intermediate in size between Dobson's Horseshoe Bat (. yunanensis) and Pearson's Horseshoe Bat (. pearsonii), are also tentatively included in this species.

opennotspecifiedOct 2019View details →
zenodo32/100

FIGURE 2 in A new species of Havelockia Pearson, 1903 from the Argentine Sea (Holothuroidea: Dendrochirotida: Sclerodactylidae)

FIGURE 2. Ossicles of Havelockia pegi sp. nov. A. Tables from body wall; B. Quadrilocular tables from tube feet; C. endplate; D. Rosettes from introvert and tentacles. Scale 50 µm.

opennotspecifiedDec 2013View details →
zenodo32/100

Subspecies and Distribution. V. v. vulpes Linnaeus, 1758 — N Europe (Scandinavia). V. v. abietorum Merriam, 1900 — SW Canada (Alberta & British Columbia). V. v. aegyptiacus Sonnini, 1816 — Egypt, Israel, and Lybia. V. v. alascensis Merriam, 1900 — Alaska and NW Canada (NW Territories & Yukon). V. v. alpheraky: Satunin, 1906 — Kazakhstan. V. v. anatolica Thomas, 1920 — Turkey. V. v. arabica Thomas, 1902 — Arabian peninsula. V. v. atlantica Wagner, 1841 — Algeria (forested Atlas Mts). V. v. bangsi Merriam, 1900 — NE Canada (Labrador). V. v. barbara Shaw, 1800 — NW Africa (Barbary Coast). V. v. beringiana Middendorff, 1875 — NE Siberia (shore of Bering Strait). V. v. cascadensis Merriam, 1900 — NW USA (Cascade Mountains, Oregon & Washington). V. v. caucasica Dinnik, 1914 — SW Russia (Caucasus). V. v. crucigera Bechstein, 1789 — Europe through N & C Russia. V. v. daurica Ognev, 1931 — E Russia (Amur, Siberia & Transbaikalia). V.v. deletrix Bangs, 1898 — NE Canada (Newfoundland). V. v. dolichocrania Ognev, 1926 — SE Siberia (S Ussuri). V. v. flavescens Gray, 1843 — N Iran. V. v. fulva Desmarest, 1820 — E USA. V. v. griffith: Blyth, 1854 — Afghanistan and N Pakistan. V.v. harrimani Merriam, 1900 — Alaska (Kodiak I). V. v. hoole Swinhoe, 1870 — S China (Fujian to Sichuan). V. v. ichnusae G. S. Miller, 1907 — Corsica and Sardinia. V. v. induta G. S. Miller, 1907 — Cyprus. V. v. jakutensis Ognev, 1923 — E Siberia (S of Yakutsk). V. v. japonica Gray, 1868 — Japan. V. v. karagan Erxleben, 1777 — Mongolia, Kazakhstan, and Kirgizstan. V. v. kenaiensis Merriam, 1900 — Alaska (Kenai Peninsula). V. v. kurdistanica Satunin, 1906 — Armenia and NE Turkey. V. v. macroura Baird, 1852 — USA (Mountain States). V. v. montana Pearson, 1836 — Himalayas form China (Yunnan) to C Pakistan. V. v. mecator Merriam, 1900 — SW USA (California & Nevada). V_ v. ochroxantha Ognev, 1926 — E Russian Turkestan, Aksai, Kirgizstan, Semirechie. V. v. palaestina Thomas, 1920 —Jordan and Lebanon. V.v. peculiosa Kishida, 1924 — Korea. V. v. pusilla Blyth, 1854 — NW India to Irak. V.v. regalis Merriam, 1900 — N Great Plains of Canada and USA. V. v. rubricosa Bangs, 1898 — E Canada. V.v. schrencki Kishida, 1924 — N Japan (Hokkaido) and NE Russia (Sakhalin). V. v. silacea G. S. Miller, 1907 — Iberian Peninsula. V.v. splendidissima Kishida, 1924 — E Russia (N & C Kurile Is). V. v. stepensis Brauner, 1914 — steppes of S Russia. V. v. tobolica Ognev, 1926 — Russia (lower basin of Ob River) V. v. tschiliensis Matschie, 1907 — NE China. Foxes of European origin were introduced into E USA and Canada in the 17" century, subsequently mixed with local subspecies. Also introduced to Australia in 1800s, and the Falkland Islands (Malvinas). in Canidae

Subspecies and Distribution. V. v. vulpes Linnaeus, 1758 — N Europe (Scandinavia). V. v. abietorum Merriam, 1900 — SW Canada (Alberta &amp; British Columbia). V. v. aegyptiacus Sonnini, 1816 — Egypt, Israel, and Lybia. V. v. alascensis Merriam, 1900 — Alaska and NW Canada (NW Territories &amp; Yukon). V. v. alpheraky: Satunin, 1906 — Kazakhstan. V. v. anatolica Thomas, 1920 — Turkey. V. v. arabica Thomas, 1902 — Arabian peninsula. V. v. atlantica Wagner, 1841 — Algeria (forested Atlas Mts). V. v. bangsi Merriam, 1900 — NE Canada (Labrador). V. v. barbara Shaw, 1800 — NW Africa (Barbary Coast). V. v. beringiana Middendorff, 1875 — NE Siberia (shore of Bering Strait). V. v. cascadensis Merriam, 1900 — NW USA (Cascade Mountains, Oregon &amp; Washington). V. v. caucasica Dinnik, 1914 — SW Russia (Caucasus). V. v. crucigera Bechstein, 1789 — Europe through N &amp; C Russia. V. v. daurica Ognev, 1931 — E Russia (Amur, Siberia &amp; Transbaikalia). V.v. deletrix Bangs, 1898 — NE Canada (Newfoundland). V. v. dolichocrania Ognev, 1926 — SE Siberia (S Ussuri). V. v. flavescens Gray, 1843 — N Iran. V. v. fulva Desmarest, 1820 — E USA. V. v. griffith: Blyth, 1854 — Afghanistan and N Pakistan. V.v. harrimani Merriam, 1900 — Alaska (Kodiak I). V. v. hoole Swinhoe, 1870 — S China (Fujian to Sichuan). V. v. ichnusae G. S. Miller, 1907 — Corsica and Sardinia. V. v. induta G. S. Miller, 1907 — Cyprus. V. v. jakutensis Ognev, 1923 — E Siberia (S of Yakutsk). V. v. japonica Gray, 1868 — Japan. V. v. karagan Erxleben, 1777 — Mongolia, Kazakhstan, and Kirgizstan. V. v. kenaiensis Merriam, 1900 — Alaska (Kenai Peninsula). V. v. kurdistanica Satunin, 1906 — Armenia and NE Turkey. V. v. macroura Baird, 1852 — USA (Mountain States). V. v. montana Pearson, 1836 — Himalayas form China (Yunnan) to C Pakistan. V. v. mecator Merriam, 1900 — SW USA (California &amp; Nevada). V_ v. ochroxantha Ognev, 1926 — E Russian Turkestan, Aksai, Kirgizstan, Semirechie. V. v. palaestina Thomas, 1920 —Jordan and Lebanon. V.v. peculiosa Kishida, 1924 — Korea. V. v. pusilla Blyth, 1854 — NW India to Irak. V.v. regalis Merriam, 1900 — N Great Plains of Canada and USA. V. v. rubricosa Bangs, 1898 — E Canada. V.v. schrencki Kishida, 1924 — N Japan (Hokkaido) and NE Russia (Sakhalin). V. v. silacea G. S. Miller, 1907 — Iberian Peninsula. V.v. splendidissima Kishida, 1924 — E Russia (N &amp; C Kurile Is). V. v. stepensis Brauner, 1914 — steppes of S Russia. V. v. tobolica Ognev, 1926 — Russia (lower basin of Ob River) V. v. tschiliensis Matschie, 1907 — NE China. Foxes of European origin were introduced into E USA and Canada in the 17" century, subsequently mixed with local subspecies. Also introduced to Australia in 1800s, and the Falkland Islands (Malvinas).

opennotspecifiedJan 2009View details →
zenodo32/100

Subspecies and Distribution. V. v. vulpes Linnaeus, 1758 — N Europe (Scandinavia). V. v. abietorum Merriam, 1900 — SW Canada (Alberta & British Columbia). V. v. aegyptiacus Sonnini, 1816 — Egypt, Israel, and Lybia. V. v. alascensis Merriam, 1900 — Alaska and NW Canada (NW Territories & Yukon). V. v. alpheraky: Satunin, 1906 — Kazakhstan. V. v. anatolica Thomas, 1920 — Turkey. V. v. arabica Thomas, 1902 — Arabian peninsula. V. v. atlantica Wagner, 1841 — Algeria (forested Atlas Mts). V. v. bangsi Merriam, 1900 — NE Canada (Labrador). V. v. barbara Shaw, 1800 — NW Africa (Barbary Coast). V. v. beringiana Middendorff, 1875 — NE Siberia (shore of Bering Strait). V. v. cascadensis Merriam, 1900 — NW USA (Cascade Mountains, Oregon & Washington). V. v. caucasica Dinnik, 1914 — SW Russia (Caucasus). V. v. crucigera Bechstein, 1789 — Europe through N & C Russia. V. v. daurica Ognev, 1931 — E Russia (Amur, Siberia & Transbaikalia). V.v. deletrix Bangs, 1898 — NE Canada (Newfoundland). V. v. dolichocrania Ognev, 1926 — SE Siberia (S Ussuri). V. v. flavescens Gray, 1843 — N Iran. V. v. fulva Desmarest, 1820 — E USA. V. v. griffith: Blyth, 1854 — Afghanistan and N Pakistan. V.v. harrimani Merriam, 1900 — Alaska (Kodiak I). V. v. hoole Swinhoe, 1870 — S China (Fujian to Sichuan). V. v. ichnusae G. S. Miller, 1907 — Corsica and Sardinia. V. v. induta G. S. Miller, 1907 — Cyprus. V. v. jakutensis Ognev, 1923 — E Siberia (S of Yakutsk). V. v. japonica Gray, 1868 — Japan. V. v. karagan Erxleben, 1777 — Mongolia, Kazakhstan, and Kirgizstan. V. v. kenaiensis Merriam, 1900 — Alaska (Kenai Peninsula). V. v. kurdistanica Satunin, 1906 — Armenia and NE Turkey. V. v. macroura Baird, 1852 — USA (Mountain States). V. v. montana Pearson, 1836 — Himalayas form China (Yunnan) to C Pakistan. V. v. mecator Merriam, 1900 — SW USA (California & Nevada). V. v. ochroxantha Ognev, 1926 — E Russian Turkestan, Aksai, Kirgizstan, Semirechie. V. v. palaestina Thomas, 1920 —Jordan and Lebanon. V.v. peculiosa Kishida, 1924 — Korea. V. v. pusilla Blyth, 1854 — NW India to Irak. V.v. regalis Merriam, 1900 — N Great Plains of Canada and USA. V. v. rubricosa Bangs, 1898 — E Canada. V.v. schrencki Kishida, 1924 — N Japan (Hokkaido) and NE Russia (Sakhalin). V. v. silacea G. S. Miller, 1907 — Iberian Peninsula. V.v. splendidissima Kishida, 1924 — E Russia (N & C Kurile Is). V. v. stepensis Brauner, 1914 — steppes of S Russia. V. v. tobolica Ognev, 1926 — Russia (lower basin of Ob River) V. v. tschiliensis Matschie, 1907 — NE China. Foxes of European origin were introduced into E USA and Canada in the 17" century, subsequently mixed with local subspecies. Also introduced to Australia in 1800s, and the Falkland Islands (Malvinas). in Canidae

Subspecies and Distribution. V. v. vulpes Linnaeus, 1758 — N Europe (Scandinavia). V. v. abietorum Merriam, 1900 — SW Canada (Alberta &amp; British Columbia). V. v. aegyptiacus Sonnini, 1816 — Egypt, Israel, and Lybia. V. v. alascensis Merriam, 1900 — Alaska and NW Canada (NW Territories &amp; Yukon). V. v. alpheraky: Satunin, 1906 — Kazakhstan. V. v. anatolica Thomas, 1920 — Turkey. V. v. arabica Thomas, 1902 — Arabian peninsula. V. v. atlantica Wagner, 1841 — Algeria (forested Atlas Mts). V. v. bangsi Merriam, 1900 — NE Canada (Labrador). V. v. barbara Shaw, 1800 — NW Africa (Barbary Coast). V. v. beringiana Middendorff, 1875 — NE Siberia (shore of Bering Strait). V. v. cascadensis Merriam, 1900 — NW USA (Cascade Mountains, Oregon &amp; Washington). V. v. caucasica Dinnik, 1914 — SW Russia (Caucasus). V. v. crucigera Bechstein, 1789 — Europe through N &amp; C Russia. V. v. daurica Ognev, 1931 — E Russia (Amur, Siberia &amp; Transbaikalia). V.v. deletrix Bangs, 1898 — NE Canada (Newfoundland). V. v. dolichocrania Ognev, 1926 — SE Siberia (S Ussuri). V. v. flavescens Gray, 1843 — N Iran. V. v. fulva Desmarest, 1820 — E USA. V. v. griffith: Blyth, 1854 — Afghanistan and N Pakistan. V.v. harrimani Merriam, 1900 — Alaska (Kodiak I). V. v. hoole Swinhoe, 1870 — S China (Fujian to Sichuan). V. v. ichnusae G. S. Miller, 1907 — Corsica and Sardinia. V. v. induta G. S. Miller, 1907 — Cyprus. V. v. jakutensis Ognev, 1923 — E Siberia (S of Yakutsk). V. v. japonica Gray, 1868 — Japan. V. v. karagan Erxleben, 1777 — Mongolia, Kazakhstan, and Kirgizstan. V. v. kenaiensis Merriam, 1900 — Alaska (Kenai Peninsula). V. v. kurdistanica Satunin, 1906 — Armenia and NE Turkey. V. v. macroura Baird, 1852 — USA (Mountain States). V. v. montana Pearson, 1836 — Himalayas form China (Yunnan) to C Pakistan. V. v. mecator Merriam, 1900 — SW USA (California &amp; Nevada). V. v. ochroxantha Ognev, 1926 — E Russian Turkestan, Aksai, Kirgizstan, Semirechie. V. v. palaestina Thomas, 1920 —Jordan and Lebanon. V.v. peculiosa Kishida, 1924 — Korea. V. v. pusilla Blyth, 1854 — NW India to Irak. V.v. regalis Merriam, 1900 — N Great Plains of Canada and USA. V. v. rubricosa Bangs, 1898 — E Canada. V.v. schrencki Kishida, 1924 — N Japan (Hokkaido) and NE Russia (Sakhalin). V. v. silacea G. S. Miller, 1907 — Iberian Peninsula. V.v. splendidissima Kishida, 1924 — E Russia (N &amp; C Kurile Is). V. v. stepensis Brauner, 1914 — steppes of S Russia. V. v. tobolica Ognev, 1926 — Russia (lower basin of Ob River) V. v. tschiliensis Matschie, 1907 — NE China. Foxes of European origin were introduced into E USA and Canada in the 17" century, subsequently mixed with local subspecies. Also introduced to Australia in 1800s, and the Falkland Islands (Malvinas).

opennotspecifiedJan 2009View details →
zenodo32/100

Subspecies and Distribution. F. c. chaus Schreber, 1777 — SE Turkey, Jordan, Israel, Lebanon, Irak, Syria, Iran, and N to the Caucasus Mountains, adjoining Russia, and E through region of Caspian and Aral Seas to W China. F. c. affinus Gray, 1830 — Sub-Himalayan region. F. c. fulvidina Thomas, 1929 — Cambodia, Laos, Vietnam, also Myanmar and Thailand. F. c. kelaarti Pocock, 1939 — S India & Sri Lanka. F. c. kutas Pearson, 1832 — N India, Pakistan, and Bangladesh. F. c. nilotica de Winton, 1898 — Egypt. in Felidae

Subspecies and Distribution. F. c. chaus Schreber, 1777 — SE Turkey, Jordan, Israel, Lebanon, Irak, Syria, Iran, and N to the Caucasus Mountains, adjoining Russia, and E through region of Caspian and Aral Seas to W China. F. c. affinus Gray, 1830 — Sub-Himalayan region. F. c. fulvidina Thomas, 1929 — Cambodia, Laos, Vietnam, also Myanmar and Thailand. F. c. kelaarti Pocock, 1939 — S India &amp; Sri Lanka. F. c. kutas Pearson, 1832 — N India, Pakistan, and Bangladesh. F. c. nilotica de Winton, 1898 — Egypt.

opennotspecifiedJan 2009View details →
zenodo32/100

On following pages: 27. Pearson's Tuco-tuco (Ctenomys pearson); 28. Perrens''s Tuco-tuco (Ctenomys perrensi); 29. Roig's Tuco-tuco (Ctenomys roigi); 30. Collared Tuco-tuco (Ctenomys torquatus); 31. Pundt's Tuco-tuco (Ctenomys pundti); 32. Talas Tuco-tuco (Ctenomys talarum); 33. Flamarion's Tuco-tuco (Ctenomys flamarioni); 34. Mendoza Tuco-tuco (Ctenomys mendocinus); 35. Cinnamon Tuco-tuco (Ctenomys porteousi); 36. Rio Negro Tuco-tuco (Ctenomys rionegrensis); 37. Dune Tuco-tuco (Ctenomys australis); 38. White-bellied Tuco-tuco (Ctenomys colburni); 39. Coyhaique Tuco-tuco (Ctenomys coyhaiquensis); 40. Lago Blanco Tuco-tuco (Ctenomys fodax); 41. Patagonian Tuco-tuco (Ctenomys haigi); 42. Magellanic Tuco-tuco (Ctenomys magellanicus); 43. Silky Tuco-tuco (Ctenomys sericeus). in Ctenomyidae

On following pages: 27. Pearson's Tuco-tuco (Ctenomys pearson); 28. Perrens''s Tuco-tuco (Ctenomys perrensi); 29. Roig's Tuco-tuco (Ctenomys roigi); 30. Collared Tuco-tuco (Ctenomys torquatus); 31. Pundt's Tuco-tuco (Ctenomys pundti); 32. Talas Tuco-tuco (Ctenomys talarum); 33. Flamarion's Tuco-tuco (Ctenomys flamarioni); 34. Mendoza Tuco-tuco (Ctenomys mendocinus); 35. Cinnamon Tuco-tuco (Ctenomys porteousi); 36. Rio Negro Tuco-tuco (Ctenomys rionegrensis); 37. Dune Tuco-tuco (Ctenomys australis); 38. White-bellied Tuco-tuco (Ctenomys colburni); 39. Coyhaique Tuco-tuco (Ctenomys coyhaiquensis); 40. Lago Blanco Tuco-tuco (Ctenomys fodax); 41. Patagonian Tuco-tuco (Ctenomys haigi); 42. Magellanic Tuco-tuco (Ctenomys magellanicus); 43. Silky Tuco-tuco (Ctenomys sericeus).

opennotspecifiedJul 2016View details →
zenodo32/100

On following pages: 729. Narrow-nasal Leaf-eared Mouse (Phyllotis stenops); 730. Pearson's Leaf-eared Mouse (Phyllotis pearson); 731. Western Leaf-eared Mouse (Phyllotis occidens); 732. Ancash Leaf-eared Mouse definitus); 733. Lima Leaf-eared Mouse (Phyllotis limatus); 734. Master Leaf-eared Mouse (Phyllotis magisten); 735. Yellow-rumped Leaf-eared Mouse (Phyllotis xanthopygus); 736. Osgood's Leaf-eared Mouse (Phyllotis (Phyllotis osgoodi); 737. Bunch Grass Leaf-eared Mouse (Phyllotis osilae); 738. Capricorn Leaf-eared Mouse (Phyllotis caprinus); 739. Tucuman Leaf-eared Mouse (Phyllotis tucumanus); 740. Walnut Leaf-eared Mouse (Phyllotis nogalaris); 741. Darwin's Leaf-eared Mouse (Phyllotis darwinii); 742. Los Alisos Leaf-eared Mouse (Phyllotis alisosiensis); 743. Anita's Leaf-eared Mouse (Phyllotis anitae); 744. Bonarian Leaf-eared Mouse (Phyllotis bonariensis), 745. Wolffsohn's Leaf-eared Mouse (Tapecomys wolffsohni); 746. Tapecua Leaf-eared Mouse (Tapecomys primus); 747. Southern Big-eared Mouse (Loxodontomys micropus); 748. Delicate Salt Flat Mouse (Salinomys delicatus), 749. Pearson's Chaco Mouse (Andalgalomys pearson); 750. Olrog's Chaco Mouse (Andalgalomys olrogi); 751. Garlepp's Mouse (Galenomys garleppi); 752. Painted Big-eared Mouse (Auliscomys pictus); 753. Bolivian Bigeared Mouse (Auliscomys boliviensis); 754. Andean Big-eared Mouse (Auliscomys sublimis); 7565. Sumichrast's Vesper Rat (Nyctomys sumichrasti); 756. Yucatan Vesper Rat (Otonyctomys hatt); 757. Big-eared Climbing Rat (Ototylomys phyllotis); 758. La Pera Climbing Rat (Ototylomys chiapensis); 759. Peters's Climbing Rat (Tylomys nudicaudus): 760. Chiapan Climbing Rat (Tylomys bullaris); 761. Tumbala Climbing Rat (Tylomys tumbalensis); 762. Watson's Climbing Rat (Tylomys watson); 763. Fulvous-bellied Climbing Rat (Tylomys fulviventen; 764. Panama Climbing Rat (Tylomys panamensis); 765. Mira Climbing Rat (Tylomys mirae). in Cricetidae

On following pages: 729. Narrow-nasal Leaf-eared Mouse (Phyllotis stenops); 730. Pearson's Leaf-eared Mouse (Phyllotis pearson); 731. Western Leaf-eared Mouse (Phyllotis occidens); 732. Ancash Leaf-eared Mouse definitus); 733. Lima Leaf-eared Mouse (Phyllotis limatus); 734. Master Leaf-eared Mouse (Phyllotis magisten); 735. Yellow-rumped Leaf-eared Mouse (Phyllotis xanthopygus); 736. Osgood's Leaf-eared Mouse (Phyllotis (Phyllotis osgoodi); 737. Bunch Grass Leaf-eared Mouse (Phyllotis osilae); 738. Capricorn Leaf-eared Mouse (Phyllotis caprinus); 739. Tucuman Leaf-eared Mouse (Phyllotis tucumanus); 740. Walnut Leaf-eared Mouse (Phyllotis nogalaris); 741. Darwin's Leaf-eared Mouse (Phyllotis darwinii); 742. Los Alisos Leaf-eared Mouse (Phyllotis alisosiensis); 743. Anita's Leaf-eared Mouse (Phyllotis anitae); 744. Bonarian Leaf-eared Mouse (Phyllotis bonariensis), 745. Wolffsohn's Leaf-eared Mouse (Tapecomys wolffsohni); 746. Tapecua Leaf-eared Mouse (Tapecomys primus); 747. Southern Big-eared Mouse (Loxodontomys micropus); 748. Delicate Salt Flat Mouse (Salinomys delicatus), 749. Pearson's Chaco Mouse (Andalgalomys pearson); 750. Olrog's Chaco Mouse (Andalgalomys olrogi); 751. Garlepp's Mouse (Galenomys garleppi); 752. Painted Big-eared Mouse (Auliscomys pictus); 753. Bolivian Bigeared Mouse (Auliscomys boliviensis); 754. Andean Big-eared Mouse (Auliscomys sublimis); 7565. Sumichrast's Vesper Rat (Nyctomys sumichrasti); 756. Yucatan Vesper Rat (Otonyctomys hatt); 757. Big-eared Climbing Rat (Ototylomys phyllotis); 758. La Pera Climbing Rat (Ototylomys chiapensis); 759. Peters's Climbing Rat (Tylomys nudicaudus): 760. Chiapan Climbing Rat (Tylomys bullaris); 761. Tumbala Climbing Rat (Tylomys tumbalensis); 762. Watson's Climbing Rat (Tylomys watson); 763. Fulvous-bellied Climbing Rat (Tylomys fulviventen; 764. Panama Climbing Rat (Tylomys panamensis); 765. Mira Climbing Rat (Tylomys mirae).

opennotspecifiedNov 2017View details →
zenodo32/100

Subspecies and Distribution. P.l.lateralisGould,1842—patchilyacrossSWesternAustralia,includingCapeRange,LittleSandyDesert,andthenearKellerberrininWheatbelt;alsoBarrowIandSalisburyI. P.l.hackettiThomas,1905—islandsofWilson,Mondrain,andWestall(RechercheArchipelago),WesternAustralia.Mayhaveoccurredhistoricallyalsoonadjacentmainland. P. l. pearson: Thomas, 1922 — North Pearson I, Investigator Group, South Australia. Introduced to South and Middle Pearson, Thistle, and Wedge Is, South Australia. A hitherto undescribed subspecies, the West Kimberley race, occurs (distributional limits uncertain) in Edgar, Grant, and Erskine Ranges and on Mt Wynne, Mt Anderson, and Mt Alexander, in S West Kimberley, Western Australia. A second undescribed subspecies, the MacDonnell Ranges race, is present in MacDonnell Ranges of C Australia, extending to E Western Australia and N South Australia. in Macropodidae

Subspecies and Distribution. P.l.lateralisGould,1842—patchilyacrossSWesternAustralia,includingCapeRange,LittleSandyDesert,andthenearKellerberrininWheatbelt;alsoBarrowIandSalisburyI. P.l.hackettiThomas,1905—islandsofWilson,Mondrain,andWestall(RechercheArchipelago),WesternAustralia.Mayhaveoccurredhistoricallyalsoonadjacentmainland. P. l. pearson: Thomas, 1922 — North Pearson I, Investigator Group, South Australia. Introduced to South and Middle Pearson, Thistle, and Wedge Is, South Australia. A hitherto undescribed subspecies, the West Kimberley race, occurs (distributional limits uncertain) in Edgar, Grant, and Erskine Ranges and on Mt Wynne, Mt Anderson, and Mt Alexander, in S West Kimberley, Western Australia. A second undescribed subspecies, the MacDonnell Ranges race, is present in MacDonnell Ranges of C Australia, extending to E Western Australia and N South Australia.

opennotspecifiedJun 2015View details →
zenodo32/100

Figure S1: Two-tailed intergroup Pearson analysis between patient age, COVID-19 detection, de-livery time, gravida, and termination week (Y-axis) with maternal and neonatal anti-COVID-19 immunoglobulins (IgG and IgM) (X-axis), depicted as a three-point color map (lowest = blue, 0 = white, highest = red) showed no significant correlation (at p>0.05).

<p>Figure S1: Two-tailed intergroup Pearson analysis between patient age, COVID-19 detection, de-livery time, gravida, and termination week (Y-axis) with maternal and neonatal anti-COVID-19 immunoglobulins (IgG and IgM) (X-axis), depicted as a three-point color map (lowest = blue, 0 = white, highest = red) showed no significant correlation (at p&gt;0.05).</p>

opencc-by-4.0Apr 2024View details →
zenodo32/100

FIGURE 3 in First record of a Lessepsian migrant: the sea cucumber Holothuria (Theelothuria) hamata Pearson, 1913

FIGURE 3. Holothuria (Theelothuria) hamata Pearson, 1913. A. Rods of tentacles; B. Tables of dorsal body wall; C. Tables of ventral body wall; D. 'Compact-look' table; E. Buttons/fenestrated ellipsoids of dorsal body wall; F. Perforated rods of papillae; G. Lateral view of tag-like tables of papillae. Scale bars B–E represent 50 mm; scale bars F&amp; G 100 mm.

opennotspecifiedJan 2019View details →
zenodo32/100

FIGURE 2 in First record of a Lessepsian migrant: the sea cucumber Holothuria (Theelothuria) hamata Pearson, 1913

FIGURE 2. Holothuria (Theelothuria) hamata Pearson, 1913. A. Dorso-lateral view; B. Ventral view (Photo's by M. Aydin)

opennotspecifiedJan 2019View details →
zenodo32/100

Fig. 4. Pearson correlation values for glucosinolate hydrolytic products. Panel A in Glucosinolate catabolism during postharvest drying determines the ratio of bioactive macamides to deaminated benzenoids in Lepidium meyenii (maca) root flour

Fig. 4. Pearson correlation values for glucosinolate hydrolytic products. Panel A shows the correlation of metabolites for the early stage of drying, where reactions are caused by direct damage to the tissue by shredding. Panel B shows the correlation between intermediaries as a result of the late stage tissue dehydration. BCOOR- 2, BCHO-2 and BCOOH-2 shown in panel B correspond to data points in Fig. 5 shown as part of the red solid line while BCOOR (8a), BCHO (5) and BCOOH (8) in panel A correspond to the early stage in the figure shown in solid black lines. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opennotspecifiedNov 2020View details →
zenodo28/100

FIGURE 3. A in A new species of Havelockia Pearson, 1903 from the Argentine Sea (Holothuroidea: Dendrochirotida: Sclerodactylidae)

FIGURE 3. A. table from body wall near anus; B. Quadrilocular table from tube foot. Scale 20 µm.

opennotspecifiedDec 2013View details →
zenodo28/100

FIGURE 1. A in A new species of Havelockia Pearson, 1903 from the Argentine Sea (Holothuroidea: Dendrochirotida: Sclerodactylidae)

FIGURE 1. A. Holotype of Havelockia pegi sp. nov., MACN-In 39019, scale 2 cm; B. Calcareous ring.

opennotspecifiedDec 2013View details →
zenodo28/100

Results of comparison among count, normalized count and pearson residual

<p>Results of comparison among count, normalized count and pearson residual</p>

opencc-by-4.0Feb 2022View details →
zenodo28/100

The Pearson correlation coefficient matrix for all study items (N = 507)

<p>The Pearson correlation coefficient matrix for all study items (N = 507)</p>

opencc-by-4.0Sep 2022View details →

ScienceDex guides

Understand access before you commit

These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

Compare curated 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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record