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.
110
datasets available to search
ShareScore release 0.9.0
Dataset results
110 results for “NEI”
Fig. 4 in New Stratigraphic Data from the Erlian Basin: Implications for the Division, Correlation, and Definition of Paleogene Lithological Units in Nei Mongol (Inner Mongolia)
Fig. 4. Above, The Arshanto Formaiton (middle beds) and Irdin Manha Formation (upper beds) at the Nuhetingboerhe locality; the arrow points to the upper hiatus between the two formatitons. Below, Close-up view of the upper hiatus showing the lithology and erosional surface.
Fig. 3 in New Stratigraphic Data from the Erlian Basin: Implications for the Division, Correlation, and Definition of Paleogene Lithological Units in Nei Mongol (Inner Mongolia)
Fig. 3. Above, Beds at the transition of the Nomogen (lower) and Arshanto (upper) at the Huheboerhe locality. Below, Close-up view of the lower hiatus showing the lithology and erosional surface between the Nomogen and Arshanto fomarions.
Fig. 2 in New Stratigraphic Data from the Erlian Basin: Implications for the Division, Correlation, and Definition of Paleogene Lithological Units in Nei Mongol (Inner Mongolia)
Fig. 2. Above, Paleogene outcrops at the Nuhetingboerhe locality. The arrow points to the lower hiatus between the Nomogen (lower) and Arshanto (upper) formations; Below, Close-up view of the lower hiatus showing the lithology and erosional surface.
Fig. 1. A in New Stratigraphic Data from the Erlian Basin: Implications for the Division, Correlation, and Definition of Paleogene Lithological Units in Nei Mongol (Inner Mongolia)
Fig. 1. A. Localities (black dots) of the Erlian Basin, Nei Mongol (Inner Mongolia). The shaded area indicates the location of the Nuhetingboerhe-Huheboerhe area (NHA). B. Topographic map of NHA. The black bars indicate positions of measured sections at the Daoteyin Obo, Nuhetingboerhe, Wulanboerhe (Huheboerhe of Meng et al., 2004), and Huheboerhe.
InMAP Source-Receptor PM2.5 Concentrations from 2014 EPA NEI
<p>These are the PM2.5 concentration datasets computed using the InMAP source-receptor (SR) matrices, with the 2014 EPA National Emissions Inventory (NEI) as inputs.</p> <p>There are 120 total files in this zip file:</p> <ol> <li>19 sectors * 5 pollutants (NH<sub>4</sub>, NO<sub>3</sub>, primary PM<sub>2.5</sub>, SO<sub>4</sub>, SOA) = 95 files, representing the <strong>contribution of each pollutant in each of those sectors to the total PM<sub>2.5</sub> concentration</strong>; these files are directly calculated from the NEI and SR matrices;</li> <li>An additional 19 files representing <strong>each sector's total contribution to the PM<sub>2.5</sub> concentration</strong>, calculated by summing together the contributions from all 5 of the pollutants for each of the 19 sectors,</li> <li>An additional 5 files representing the <strong>overall PM<sub>2.5</sub> concentration across all sectors</strong>, calculated by summing together the contributions from all of the 19 sectors, for each of the 5 pollutants,</li> <li>An additional 1 file representing the <strong>overall total PM<sub>2.5</sub> concentration across all sectors and pollutants</strong>, calculated by summing together the contributions of all 19 sectors and all 5 pollutants.</li> </ol> <p>Every file is saved as a .mat file and can be loaded into MATLAB using the load() function. Each .mat file has dimensions of 52411x1, where each value represents a PM<sub>2.5</sub> concentration in one of the 52411 InMAP grid cells. You will need to download the InMAP grid shapefile in order to project and map this data.</p>
FIG. 9 in New ctenodactyloid rodents from the Erlian Basin, Nei Mongol, China, and the phylogenetic relationships of Eocene Asian ctenodactyloids
FIG. 9. Occlusal view of a maxillary fragment of Tamquammys fractus with P4–M2.
Materiali aggiuntivi per lavoro su prevedibilità nei paradigmi verbali dell'italiano
<p>Sono qui resi disponibili, in formato .csv, i dati di partenza e i risultati con essi ottenuti relativamente all'articolo "Dai temi alle forme: zone paradigmatiche nella flessione verbale dell’italiano", sulla rivista "Études romanes de Brno".<br>Nel dettaglio, sono presenti:<br>1. una cartella contenente l'intero dataset -- che corrisponde al lessico LeFFI, v1.1 (https://github.com/matteo-pellegrini/LeFFI/releases/tag/v1.1), i pattern estratti da tale dataset e i valori di entropia ottenuti (cfr. Tabelle 11, 12 e 15 dell'articolo);<br>2. una cartella contenente il dataset 1. senza alcuni verbi irregolari e i loro derivati, i pattern estratti da tale dataset e i valori di entropia ottenuti (cfr. Tabelle 19 e 21 dell'articolo);<br>3. una cartella contenente il dataset 2. senza notazione dell'accento e con 8 colonne agguntive in cui è riportata la forma dei diversi temi di ciascun lessema, i pattern estratti da tale dataset e i valori di entropia ottenuti (utilizzato per il confronto tra entropia basata sulle forme e sui temi, cfr. Figura 4 dell'articolo);<br>4. un documento in cui si riporta l'inventario di suoni utilizzato, in cui ciascun suono è caratterizzato da una combinazione di tratti fonologici distintivi.</p>
Fig. 5 in Gomphos elkema (Glires, Mammalia) from the Erlian Basin: Evidence for the Early Tertiary Bumbanian Land Mammal Age in Nei-Mongol, China
Fig. 5. Lower teeth of Gomphos elkema. A–C. Occlusal, lingual, and labial views of right m1–m3
Fig. 6 in Gomphos elkema (Glires, Mammalia) from the Erlian Basin: Evidence for the Early Tertiary Bumbanian Land Mammal Age in Nei-Mongol, China
Fig. 6. Lower teeth of Gomphos elkema. A–B. Occlusal views of left and right m1–m3, respectively
Fig. 1 in Gomphos elkema (Glires, Mammalia) from the Erlian Basin: Evidence for the Early Tertiary Bumbanian Land Mammal Age in Nei-Mongol, China
Fig. 1. Locality map of the Erlian Basin (after Meng et al., 1998).
Fig. 7. Sketch profile from the locality 10 in New Stratigraphic Data from the Erlian Basin: Implications for the Division, Correlation, and Definition of Paleogene Lithological Units in Nei Mongol (Inner Mongolia)
Fig. 7. Sketch profile from the locality 10 miles southwest of the Camp Margetts (Granger, 1930).
Subspecies and Distribution. C.b.bactrianusLinnaeus,1758—aridlandsanddesertsofC&SAsiaasdomesticatedlivestock. C. b. ferus Przewalski, 1878 — NW China (C & SE Xinjiang, Nei Mongol, NW Qinghai & NW Gansu) and Mongolia. in Camelidae
Subspecies and Distribution. C.b.bactrianusLinnaeus,1758—aridlandsanddesertsofC&SAsiaasdomesticatedlivestock. C. b. ferus Przewalski, 1878 — NW China (C & SE Xinjiang, Nei Mongol, NW Qinghai & NW Gansu) and Mongolia.
Distribution. NE Kazakhstan, SC & SE Russia (including Sakhalin I), N Mongolia, NE Cina (Nei Mongol, TE Jilin, and Liaoning), Korean Peninsula (including Jeju I), much ofJapan (Hokkaido, Honshu, Okushiri, and Rishirito Is), and S Kuril Is (Kunashir) in Vespertilionidae
Distribution. NE Kazakhstan, SC & SE Russia (including Sakhalin I), N Mongolia, NE Cina (Nei Mongol, TE Jilin, and Liaoning), Korean Peninsula (including Jeju I), much ofJapan (Hokkaido, Honshu, Okushiri, and Rishirito Is), and S Kuril Is (Kunashir)
Subspecies and Distribution. E.p.pachyomusTomes,1857—SEIran,NEAfghanistan,NPakistan,extremeSWChina(Tibet[=Xizang]),NIndia(JammuandKashmirEtoNagaland),Nepal,andBhutan. E.p.andersoniDobson,1871—EMyanmar,C,SC&SEChina(Sichuan,Yunnan,Guizhou,Hunan,Jiangxi,Anhui,Jiangsu,Shanghai,Zhejiang,andFujian),NThailand,NLaos,andNVietnam. E.p.horikawaiKishida,1924—TaiwanI. E. p. pallens G. S. Miller, 1911 — S Mongolia, NC, NE, C & E China (Gansu, Inner Mongolia [= Nei Mongol], Heilongjiang, Jilin, Liaoning, Sichuan, Ningxia, Shaanxi, Shanxi, Hebei, Beijing, Tianjin, Shandong, Henan, Hubei, Anhui, andJiangsu), and Korean Peninsula. in Vespertilionidae
Subspecies and Distribution. E.p.pachyomusTomes,1857—SEIran,NEAfghanistan,NPakistan,extremeSWChina(Tibet[=Xizang]),NIndia(JammuandKashmirEtoNagaland),Nepal,andBhutan. E.p.andersoniDobson,1871—EMyanmar,C,SC&SEChina(Sichuan,Yunnan,Guizhou,Hunan,Jiangxi,Anhui,Jiangsu,Shanghai,Zhejiang,andFujian),NThailand,NLaos,andNVietnam. E.p.horikawaiKishida,1924—TaiwanI. E. p. pallens G. S. Miller, 1911 — S Mongolia, NC, NE, C & E China (Gansu, Inner Mongolia [= Nei Mongol], Heilongjiang, Jilin, Liaoning, Sichuan, Ningxia, Shaanxi, Shanxi, Hebei, Beijing, Tianjin, Shandong, Henan, Hubei, Anhui, andJiangsu), and Korean Peninsula.
Distribution. SE Mongolia, NE, E & C China (Gansu, Ningxia, Inner Mongolia [= Nei Mongol], Heilongjiang, Jilin, Liaoning, Sichuan, Henan, Shandong, and Anhui), S Russian Far East, Korean Peninsula (includingJeju I), andJapan (S Hokkaido, N Honshu, and Tsushima Is). in Vespertilionidae
Distribution. SE Mongolia, NE, E & C China (Gansu, Ningxia, Inner Mongolia [= Nei Mongol], Heilongjiang, Jilin, Liaoning, Sichuan, Henan, Shandong, and Anhui), S Russian Far East, Korean Peninsula (includingJeju I), andJapan (S Hokkaido, N Honshu, and Tsushima Is).
Distribution. It was restricted to NE China. Most extant museum specimens purported to be jubata were collected in the mountain ranges N of Hohot, Nei Mongol S of the Mongolian border. in Bovidae
Distribution. It was restricted to NE China. Most extant museum specimens purported to be jubata were collected in the mountain ranges N of Hohot, Nei Mongol S of the Mongolian border.
Distribution. China (S Xinjiang, Qinghai, Gansu, S Nei Mongol, Ningxia, Shaanxi, Sichuan, Xizang & N Yunnan), N Pakistan, N India, Nepal, Bhutan, and N Myanmar. in Bovidae
Distribution. China (S Xinjiang, Qinghai, Gansu, S Nei Mongol, Ningxia, Shaanxi, Sichuan, Xizang & N Yunnan), N Pakistan, N India, Nepal, Bhutan, and N Myanmar.
Distribution. Disjunct locations in NE China (Liaoning, Inner Mongolia [= Nei Mongol], Hebei, Beijing, and Shandong), N & C Laos, and NE Thailand (Loei Province). There are three vagrant records in Japan, on Amami-Oshima, Kuchinoerabujima, and Yoronjima Is. in Molossidae
Distribution. Disjunct locations in NE China (Liaoning, Inner Mongolia [= Nei Mongol], Hebei, Beijing, and Shandong), N & C Laos, and NE Thailand (Loei Province). There are three vagrant records in Japan, on Amami-Oshima, Kuchinoerabujima, and Yoronjima Is.
Subspecies and Distribution. pos sagitta Pallas, 1773 — S Russia (Altai Krai) and right bank of Irtysh River in Kazakhstan (Pavlodar and East Kazakhstan regions). D.s.aksuensisWangSung,1964—NWChina(NTarimBasininXinjiang). D.s.austrouralensisShenbrot,1991—NWKazakhstan(WestKazakhstan,Atyrau,andAktoberegionsbetweenUralandEmbarivers). D.s.bulganensisShenbrot,1991—EKazakhstan(ELakeZaysaninEastKazakhstanRegion),NWChina(DzungarianBasininXinjiang),andMongolia(SKhovdandSWGovi-Altai). D.s.deasyiBarret-Hamilton,1900—NWChina(STarimBasininXinjiangandS&WQaidamBasininQinghai). D. s. fuscocanus Wang Sung, 1964 — W China (S foothills of E Tian Shan in Xinjiang). D. s. halli Sowerby, 1920 — China (NE Inner Mongolia [= Nei Mongol], SW Heilongjiang, NWJilin, and N Liaoning) and SE Mongolia (Stikhbaatar). D. s. innae Ognev, 1930 — S Russia (Astrakhan Region E of Volga River) and NW Kazakhstan (West Kazakhstan and Atyrau regions W of Ural River). D. s. lagopus Lichtenstein, 1823 — WC Kazakhstan (E of Emba and N of Syrdarya rivers). D. s. megacranius Shenbrot, 1991 — SE Kazakhstan (Moinkum Sands in Jambyl Region). D. s. nogai Satunin, 1907 — S European Russia (Volgograd and Astrakhan regions E of Volga River, Kalmykia, and Dagestan). D. s. sowerbyi Thomas, 1908 — N China (NE Xinjiang, N Qaidam Basin in Qinghai, Gansu, SW Inner Mongolia, N Ningxia, and N Shaanxi) and Mongolia. D. s. turanicus Shenbrot, 1991 — SW Kazakhstan (S Kyzylorda S of Syrdarya River and Mangystau regions), Uzbekistan, and Turkmenistan; it probably occurs in adjacent W Afghanistan. D. s. ubsanensis Bannikov, 1947 — NW Mongolia (N Uvs) and adjacent Russia (extreme S Tuva). D. s. usuni Shenbrot, 1991 — SE Kazakhstan (Almaty Region); it probably occurs in adjacent China (sands of Ili Valley of W Xinjiang). D. s. zaissanensis Selevin, 1934 — E Kazakhstan (NW Lake Zaysan Basin on the left bank of Irtysh River). Isolated population in N Iran (Turan Desert in E Semnan Province) may belong to turanicus or correspond to a yet undescribed subspecies. in Dipodidae
Subspecies and Distribution. pos sagitta Pallas, 1773 — S Russia (Altai Krai) and right bank of Irtysh River in Kazakhstan (Pavlodar and East Kazakhstan regions). D.s.aksuensisWangSung,1964—NWChina(NTarimBasininXinjiang). D.s.austrouralensisShenbrot,1991—NWKazakhstan(WestKazakhstan,Atyrau,andAktoberegionsbetweenUralandEmbarivers). D.s.bulganensisShenbrot,1991—EKazakhstan(ELakeZaysaninEastKazakhstanRegion),NWChina(DzungarianBasininXinjiang),andMongolia(SKhovdandSWGovi-Altai). D.s.deasyiBarret-Hamilton,1900—NWChina(STarimBasininXinjiangandS&WQaidamBasininQinghai). D. s. fuscocanus Wang Sung, 1964 — W China (S foothills of E Tian Shan in Xinjiang). D. s. halli Sowerby, 1920 — China (NE Inner Mongolia [= Nei Mongol], SW Heilongjiang, NWJilin, and N Liaoning) and SE Mongolia (Stikhbaatar). D. s. innae Ognev, 1930 — S Russia (Astrakhan Region E of Volga River) and NW Kazakhstan (West Kazakhstan and Atyrau regions W of Ural River). D. s. lagopus Lichtenstein, 1823 — WC Kazakhstan (E of Emba and N of Syrdarya rivers). D. s. megacranius Shenbrot, 1991 — SE Kazakhstan (Moinkum Sands in Jambyl Region). D. s. nogai Satunin, 1907 — S European Russia (Volgograd and Astrakhan regions E of Volga River, Kalmykia, and Dagestan). D. s. sowerbyi Thomas, 1908 — N China (NE Xinjiang, N Qaidam Basin in Qinghai, Gansu, SW Inner Mongolia, N Ningxia, and N Shaanxi) and Mongolia. D. s. turanicus Shenbrot, 1991 — SW Kazakhstan (S Kyzylorda S of Syrdarya River and Mangystau regions), Uzbekistan, and Turkmenistan; it probably occurs in adjacent W Afghanistan. D. s. ubsanensis Bannikov, 1947 — NW Mongolia (N Uvs) and adjacent Russia (extreme S Tuva). D. s. usuni Shenbrot, 1991 — SE Kazakhstan (Almaty Region); it probably occurs in adjacent China (sands of Ili Valley of W Xinjiang). D. s. zaissanensis Selevin, 1934 — E Kazakhstan (NW Lake Zaysan Basin on the left bank of Irtysh River). Isolated population in N Iran (Turan Desert in E Semnan Province) may belong to turanicus or correspond to a yet undescribed subspecies.
Subspecies and Distribution. S.c.crassicaudaVinogradov,1924—EKazakhstan(LakeZaysanBasin),NWChina(NXinjiang),andSWMongolia. S. c. gobicus Sokolov & Shenbrot, 1988 — S & SE Mongolia and N China (N Gansu and W Inner Mongolia [= Nei Mongol]). in Dipodidae
Subspecies and Distribution. S.c.crassicaudaVinogradov,1924—EKazakhstan(LakeZaysanBasin),NWChina(NXinjiang),andSWMongolia. S. c. gobicus Sokolov & Shenbrot, 1988 — S & SE Mongolia and N China (N Gansu and W Inner Mongolia [= Nei Mongol]).
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.