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zenodo32/100

A calcium-based plasticity model for predicting long-term potentiation and depression in the neocortex

<p>This dataset contains all (&gt;1000) cell pairs as the Blue Brain Projects <a href="https://github.com/BlueBrain/EModelRunner">EModelRunner</a> packages as well as analysis code and analysed data used for the figures of our <a href="https://www.biorxiv.org/content/biorxiv/early/2020/04/20/2020.04.19.043117.full.pdf">preprint</a>: <em><strong>&quot;A calcium-based plasticity model predicts long-term potentiation and depression in the neocortex&quot;</strong></em>.</p> <p>More documentation will follow in the upcoming days.</p> <p><strong>Updates:</strong><br> v1.1 (31/12/2021): updated READMEs within cell_packages, added 2 extra authors for their contribution in EModelRunner.<br> v1.2 (31/12/2021): same as v1.1 but w/o MacOS junk<br> v1.3 (11/01/2022): added analysis notebooks<br> v2.0 (11/01/2022): same as v1.3 but w/o MacOS junk and proper version number<br> v2.1 (14/03/2022): fetching data from websites when possible instead of providing the downloaded csv files.</p>

opencc-by-4.0Nov 2021View details →
zenodo32/100

Supplementary material 1 from: Di Lorenzo T, Di Marzio W, Piccini L, Messana G, Sáenz M, Galassi D (2018) Survival, metabolic rates and locomotory activities of a groundwater-obligate copepod species under long-term exposures to tetrachloroethylene. ARPHA Conference Abstracts 1: e29966. https://doi.org/10.3897/aca.1.e29966

Survival, metabolic rates and locomotory activities of a groundwater-obligate copepod species under long-term exposures to tetrachloroethylene

opencc-zeroMar 2022View details →
dryad32/100

Archive data supporting the results in the paper: Long-term soil warming alters fine root dynamics and morphology, and their ectomycorrhizal fungal community in a temperate forest soil"

<p><span>Climate warming is predicted to affect temperate forests severely, but the response of fine roots, key to plant nutrition, water uptake, soil carbon and nutrient cycling is unclear. Understanding how fine roots will respond to increasing temperature is a prerequisite for predicting the functioning of forests in a warmer climate. We studied the response of fine roots and their ectomycorrhizal (EcM) fungal and root-associated bacterial communities to soil warming by 4 °C in a mixed spruce-beech forest in the Austrian Limestone Alps after 8 and 14 years of soil warming, respectively. Fine root biomass (FRB) and fine root production were 17% and 128% higher in the warmed plots, respectively, after 14 years. The increase in FRB (13%) was not significant after 8 years of treatment, whereas specific root length, specific root area, and root tip density were significantly higher in warmed plots at both sampling occasions. Soil warming did not affect EcM exploration types and diversity, but changed their community composition, with an increase in the relative abundance of <em>Cenoccocum</em> at 0 – 10 cm soil depth, a drought-stress tolerant genus, and an increase in short and long-distance exploration types like <em>Sebacina </em>and <em>Boletus </em>at 10 – 20 cm soil depth. Warming increased the root-associated bacterial diversity but did not affect their community composition. Soil warming did not affect nutrient concentrations of fine roots, though we found indications of limited soil phosphorus (P) and potassium (K) availability. </span><span>Our findings suggest that, in the studied ecosystem, global warming could persistently increase soil carbon inputs due to accelerated fine root growth and turnover, and could simultaneously alter fine root morphology and EcM fungal community composition towards improved nutrient foraging. </span></p>

opencc-zeroMar 2022View details →
zenodo32/100

On following pages: 42. Steppe Polecat (Mustela eversmanii); 43. Colombian Weasel (Mustela felipei); 44. Long-tailed Weasel (Mustela frenata); 45. Japanese Weasel (Mustela itatsi); 46. Yellow-bellied Weasel (Mustela kathiah); 47. European Mink (Mustela lutreola); 48. Indonesian Mountain Weasel (Mustela lutreolina); 49. Black-footed Ferret (Mustela nigripes); 50. Least Weasel (Mustela nivalis); 51. Malay Weasel (Mustela nudipes); 52. European Polecat (Mustela putorius); 53. Siberian Weasel (Mustela sibirica); 54. Back-striped Weasel (Mustela strigidorsa); 55. Egyptian Weasel (Mustela subpalmata); 56. American Mink (Neovison vison); 57. Patagonian in Mustelidae

On following pages: 42. Steppe Polecat (Mustela eversmanii); 43. Colombian Weasel (Mustela felipei); 44. Long-tailed Weasel (Mustela frenata); 45. Japanese Weasel (Mustela itatsi); 46. Yellow-bellied Weasel (Mustela kathiah); 47. European Mink (Mustela lutreola); 48. Indonesian Mountain Weasel (Mustela lutreolina); 49. Black-footed Ferret (Mustela nigripes); 50. Least Weasel (Mustela nivalis); 51. Malay Weasel (Mustela nudipes); 52. European Polecat (Mustela putorius); 53. Siberian Weasel (Mustela sibirica); 54. Back-striped Weasel (Mustela strigidorsa); 55. Egyptian Weasel (Mustela subpalmata); 56. American Mink (Neovison vison); 57. Patagonian

opennotspecifiedJan 2009View details →
zenodo32/100

On following pages: 42. Steppe Polecat (Mustela eversmanii); 43. Colombian Weasel (Mustela felipei); 44. Long-tailed Weasel (Mustela frenata); 45. Japanese Weasel (Mustela itatsi); 46. Yellow-bellied Weasel (Mustela kathiah); 47. European Mink (Mustela lutreola); 48. Indonesian Mountain Weasel (Mustela lutreolina); 49. Black-footed Ferret (Mustela nigripes); 50. Least Weasel (Mustela nivalis); 51. Malay Weasel (Mustela nudipes); 52. European Polecat (Mustela putorius); 53. Siberian Weasel (Mustela sibirica); 54. Back-striped Weasel (Mustela strigidorsa); 55. Egyptian Weasel (Mustela subpalmata); 56. American Mink (Neovison vison); 57. Patagonian Weasel (Lyncodon patagonicus). in Mustelidae

On following pages: 42. Steppe Polecat (Mustela eversmanii); 43. Colombian Weasel (Mustela felipei); 44. Long-tailed Weasel (Mustela frenata); 45. Japanese Weasel (Mustela itatsi); 46. Yellow-bellied Weasel (Mustela kathiah); 47. European Mink (Mustela lutreola); 48. Indonesian Mountain Weasel (Mustela lutreolina); 49. Black-footed Ferret (Mustela nigripes); 50. Least Weasel (Mustela nivalis); 51. Malay Weasel (Mustela nudipes); 52. European Polecat (Mustela putorius); 53. Siberian Weasel (Mustela sibirica); 54. Back-striped Weasel (Mustela strigidorsa); 55. Egyptian Weasel (Mustela subpalmata); 56. American Mink (Neovison vison); 57. Patagonian Weasel (Lyncodon patagonicus).

opennotspecifiedJan 2009View details →
zenodo32/100

Is switchgrass good for carbon savings? Long-term results in marginal land Running title: Switchgrass SOC storage capacity in marginal land Walter Zegada-Lizarazu 1, Federica Zanetti 1, Nicola Di Virgilio 2, Andrea Monti 1 1Department of Agricultural and Food Sciences, University of Bologna, Viale G. Fanin 44 – 40127, Bologna, Italy; 2CNR, Institute for the BioEcononomy, National Research Council of Italy, Via P Gobetti 101, I-40129 Bologna, Italy

<p>Growing switchgrass in marginal land can be a valuable option to mitigate the risk of agricultural land abandonment whilst storing a significant amount of soil C. It was found a significant increase in SOC in a 13-years period. A significant positive correlation was observed between the C derived from switchgrass and SOC gain (the estimated switchgrass derived C was 12.7 Mg C ha<sup>-1</sup>). The increased SOC along the field, however, was patchy, with the highest increments registered in the center of the field, while the lowest ones in the top and bottom of the hill.</p>

opencc-byMar 2022View details →
zenodo32/100

AERA5-Asia: A long-term Asian precipitation dataset (0.1°, 1 hourly, 1951–2015, Asia) anchoring the ERA5-Land under the total volume control by APHRODITE (1967–1981)

<p>AERA5-Asia: A long-term Asian precipitation dataset (0.1&deg;, 1 hourly, 1951&ndash;2015, Asia) is developed by organically combining the ERA5-Land dataset with high spatiotemporal resolutions and continuity and the APHRODITE dataset with high quality.</p> <p><strong>How to cite:&nbsp;Ma, Z., Xu, J., Ma, Y., Zhu, S., He, K., Zhang, S., Ma, W., Xu, X., 2022. AERA5-Asia: A long-term Asian precipitation dataset (0.1&deg;, 1 hourly, 1951&ndash;2015, Asia) anchoring the ERA5-Land under the total volume control by APHRODITE. Bulletin of American Meteorological Society, 103 (4)., DOI: https://doi.org/10.1175/BAMS-D-20-0328.1.</strong></p> <p>Data Format:&nbsp;GeoTIFF</p> <p>Spatial Coverage: 60&deg;E&ndash;150&deg;E, 15&deg;S&ndash;55&deg;N, land.</p> <p>AERA5-Asia (0.1&deg;/ hourly, 1951&ndash;1966,&nbsp;Asia) is available at&nbsp;&nbsp;<a href="https://doi.org/10.5281/zenodo.3609352">https://doi.org/</a><a href="https://doi.org/10.5281/zenodo.4266081">10.5281/zenodo.6367463</a></p> <p>AERA5-Asia (0.1&deg;/ hourly, 1982&ndash;1998,&nbsp;Asia) is available at&nbsp;&nbsp;<a href="https://doi.org/10.5281/zenodo.3609352">https://doi.org/</a><a href="https://doi.org/10.5281/zenodo.4266081">10.5281/zenodo.4266081</a></p> <p>AERA5-Asia (0.1&deg;/ hourly, 1999&ndash;2015,&nbsp;Asia) is available at&nbsp;&nbsp;<a href="https://doi.org/10.5281/zenodo.3609352">https://doi.org/</a><a href="https://doi.org/10.5281/zenodo.4264451">10.5281/zenodo.4264451</a></p>

opencc-by-4.0Nov 2020View details →
zenodo32/100

AERA5-Asia: A long-term Asian precipitation dataset (0.1°, 1 hourly, 1951–2015, Asia) anchoring the ERA5-Land under the total volume control by APHRODITE (1951–1966)

<p>AERA5-Asia: A long-term Asian precipitation dataset (0.1&deg;, 1 hourly, 1951&ndash;2015, Asia) is developed by organically combining the ERA5-Land dataset with high spatiotemporal resolutions and continuity and the APHRODITE dataset with high quality.</p> <p><strong>How to cite:&nbsp;Ma, Z., Xu, J., Ma, Y., Zhu, S., He, K., Zhang, S., Ma, W., Xu, X., 2022. AERA5-Asia: A long-term Asian precipitation dataset (0.1&deg;, 1 hourly, 1951&ndash;2015, Asia) anchoring the ERA5-Land under the total volume control by APHRODITE. Bulletin of American Meteorological Society, 103 (4)., DOI: https://doi.org/10.1175/BAMS-D-20-0328.1.</strong></p> <p>Data Format:&nbsp;GeoTIFF</p> <p>Spatial Coverage: 60&deg;E&ndash;150&deg;E, 15&deg;S&ndash;55&deg;N, land.</p> <p>AERA5-Asia (0.1&deg;/ hourly, 1962&ndash;1981,&nbsp;Asia) is available at&nbsp;&nbsp;<a href="https://doi.org/10.5281/zenodo.3609352">https://doi.org/</a><a href="https://doi.org/10.5281/zenodo.4266081">10.5281/zenodo.6369796</a></p> <p>AERA5-Asia (0.1&deg;/ hourly, 1982&ndash;1998,&nbsp;Asia) is available at&nbsp;&nbsp;<a href="https://doi.org/10.5281/zenodo.3609352">https://doi.org/</a><a href="https://doi.org/10.5281/zenodo.4266081">10.5281/zenodo.4266081</a></p> <p>AERA5-Asia (0.1&deg;/ hourly, 1999&ndash;2015,&nbsp;Asia) is available at&nbsp;&nbsp;<a href="https://doi.org/10.5281/zenodo.3609352">https://doi.org/</a><a href="https://doi.org/10.5281/zenodo.4264451">10.5281/zenodo.4264451</a></p>

opencc-by-4.0Nov 2020View details →
zenodo32/100

FIGURE. Floral habit and structure of C. spongifolia. A. Type specimen in situ with open, spathe limb (apex is reflexed out of view), and green spathe tube (ca. 6 cm long). B. Adjacent plant with inflorescences and prophylls. C. Spadix showing from top: sterile appendix, staminate (male) zone, sterile interstice, and green pistillate (female) zone with tapered, conical form. D. Detail of female zone showing a few basal staminodes. E–G. Berries of the preserved type specimen. G. Dissected berry with orthotropous ovules (some outlined) attached by funicles to parietal placentae (arrows). H. Surface of male zone showing closely-packed synandria. I. Synandria separated to show fused anther sacs beneath apical pores (example in center has 8 pores, 8 anthers) J. Mature fruiting head, with single berry removed to show seed packing and 67 seeds extracted (scale bar units: 1 mm) (Bach Ma NP; type 2020; fruit and seeds 2018). Photos: NVD and PJM. in Colocasia spongifolia sp. nov. (Araceae) in southern China and central Vietnam

FIGURE. Floral habit and structure of C. spongifolia. A. Type specimen in situ with open, spathe limb (apex is reflexed out of view), and green spathe tube (ca. 6 cm long). B. Adjacent plant with inflorescences and prophylls. C. Spadix showing from top: sterile appendix, staminate (male) zone, sterile interstice, and green pistillate (female) zone with tapered, conical form. D. Detail of female zone showing a few basal staminodes. E–G. Berries of the preserved type specimen. G. Dissected berry with orthotropous ovules (some outlined) attached by funicles to parietal placentae (arrows). H. Surface of male zone showing closely-packed synandria. I. Synandria separated to show fused anther sacs beneath apical pores (example in center has 8 pores, 8 anthers) J. Mature fruiting head, with single berry removed to show seed packing and 67 seeds extracted (scale bar units: 1 mm) (Bach Ma NP; type 2020; fruit and seeds 2018). Photos: NVD and PJM.

opennotspecifiedMar 2022View details →
dryad32/100

Data from: Determinants and long-term costs of early reproduction in males of a long-lived polygynous mammal

<p>In long-lived polygynous species, male reproductive success is often monopolized by a few mature dominant individuals. Young males are generally too small to be dominant and may employ alternative tactics, however, little is known about the determinants of reproductive success for young males. Understanding the causes and consequences of variability in early reproductive success may be crucial to assess the strength of sexual selection and possible long-term trade-offs among life-history traits. Selective pressures driven by fluctuating environmental conditions may depend on age-class. We evaluated the determinants of reproduction in male bighorn sheep (<em>Ovis canadensis</em>) aged 2-4 years using 30 years of individual-level data. These young males cannot defend estrous ewes and use alternative mating tactics. We also investigated how the age of first detected reproduction was correlated to lifetime reproductive success and longevity. We found that reproductive success of males aged three years was positively correlated to body mass, to the proportion of males aged 2-4 years in the competitor pool and to the number of females available per adult male. These results suggest that reproductive success depends on both competitive ability and population age-sex structure. None of these variables, however, had significant effects on the reproductive success of males aged 2 or 4 years. Known reproduction before the age of five increased lifetime reproductive success but decreased longevity, suggesting a long-term survival cost of early reproduction. Our analyses reveal that both individual-level phenotypic and population-level demographic variables influence reproductive success by young males and provide a rare assessment of fitness trade-offs in wild polygynous males.</p>

opencc-zeroMar 2022View details →
zenodo32/100

X-ray investigation of long-range antiferromagnetic ordering in FeRh

<p>Open data to &quot;X-ray investigation of long-range antiferromagnetic ordering in FeRh&quot; published in AIP Advances <strong>12</strong>, 035048 (2022); <a href="https://doi.org/10.1063/9.0000320">https://doi.org/10.1063/9.0000320</a></p>

opencc-by-4.0Dec 2021View details →
zenodo32/100

TPM quantification (StringTie) of long-read isoforms in TCGA breast tumors and GTEx

<p>StringTie was applied to quantify the expression of long-read isoforms sequenced in TCGA and GTEx samples.</p> <p>Inputs:</p> <ul> <li>RNA-seq samples (bam files) from breast cancer samples from TCGA (tumors) and GTEx tissues (healthy controls).</li> <li>GTF: full-length isoforms sequenced using PacBio long-read sequencing in breast tumors. See&nbsp;<a href="https://www.science.org/doi/10.1126/sciadv.abg6711">A comprehensive long-read isoform analysis platform and sequencing resource for breast cancer</a>.</li> </ul> <p>Output: tab-delimited files with TPM values for isoforms parsed from StringTie results.</p> <p>More details:&nbsp;<a href="https://www.science.org/doi/10.1126/sciadv.abg6711">A comprehensive long-read isoform analysis platform and sequencing resource for breast cancer</a></p> <p>&nbsp;</p> <p>&nbsp;</p> <p>&nbsp;</p> <p>&nbsp;</p>

opencc-by-4.0Mar 2022View details →
zenodo32/100

On following pages: 477. Fringed Long-footed Myotis (Myotis fimbriatus); 478. Rickett's Big-footed Myotis (Myotis pilosus); 479. Mandelli's Myotis (Myotis sicarius); 480. Bechstein's Myotis (Myotis bechsteinii): 481. Long-tailed Myotis (Myotis longicaudatus); 482. Daubenton's Myotis (Myotis daubentonii); 483. Reddish Myotis (Myotis soror); 484. Fraternal Myotis (Myotis fraten; 485. Bokhara Myotis (Myotis bucharensis); 486. Lesser Myotis (Myotis blythii); 487. Greater Myotis (Myotis myotis); 488. Maghreb Myotis (Myotis punicus); 489. Natterer's Myotis (Myotis nattereri); 490. Cryptic Myotis (Myotis crypticus); 491. Schaub's Myotis (Myotis schaubi); 492. Escalera's Myotis (Myotis escaleral), 493. Zenati Myotis (Myotis zenatius); 494. Peking Myotis (Myotis pequinius); 495. Far Eastern Myotis (Myotis bombinus); 496. Large Myotis (Myotis chinensis). in Vespertilionidae

On following pages: 477. Fringed Long-footed Myotis (Myotis fimbriatus); 478. Rickett's Big-footed Myotis (Myotis pilosus); 479. Mandelli's Myotis (Myotis sicarius); 480. Bechstein's Myotis (Myotis bechsteinii): 481. Long-tailed Myotis (Myotis longicaudatus); 482. Daubenton's Myotis (Myotis daubentonii); 483. Reddish Myotis (Myotis soror); 484. Fraternal Myotis (Myotis fraten; 485. Bokhara Myotis (Myotis bucharensis); 486. Lesser Myotis (Myotis blythii); 487. Greater Myotis (Myotis myotis); 488. Maghreb Myotis (Myotis punicus); 489. Natterer's Myotis (Myotis nattereri); 490. Cryptic Myotis (Myotis crypticus); 491. Schaub's Myotis (Myotis schaubi); 492. Escalera's Myotis (Myotis escaleral), 493. Zenati Myotis (Myotis zenatius); 494. Peking Myotis (Myotis pequinius); 495. Far Eastern Myotis (Myotis bombinus); 496. Large Myotis (Myotis chinensis).

opennotspecifiedOct 2019View details →
zenodo32/100

On following pages: 452. Long-toed Myotis (Myotis secundus); 453. Bornean Whiskered Myotis (Myotis borneoensis); 454. Malaysian Whiskered Myotis (Myotis federatus): 455. Indochinese Myotis (Myotis indochinensis); 456. Peyton's Myotis (Myotis peyton); 457. Burmese Whiskered Myotis (Myotis montivagus); 458. Long-fingered Myotis (Myotis capaccinii); 459. Chinese Water Myotis (Myotis laniger); 460. Csorba's Myotis (Myotis csorbal); 461. Kashmir Cave Myotis (Myotis longipes); 462. Annamit Myotis (Myotis annamiticus); 463. Phan Luong's Myotis (Myotis phanluongi); 464. Himalayan Whiskered Myotis (Myotis siligorensis); 465. Chestnut Myotis (Myotis badius); 466. Ridley's Myotis (Myotis ridley); 467. Thick-thumbed Myotis (Myotis rosseti); 468. Horsfield's Myotis (Myotis horsfieldi); 469. Pallid Large-footed Myotis (Myotis macrotarsus); 470. Stalker's Myotis (Myotis stalkeri); 471. Gray Large-footed Myotis (Myotis adversus); 472. Maluku Myotis (Myotis moluccarum); 473. Southern Myotis (Myotis macropus); 474. Lesser Large-footed Myotis (Myotis hasselti). in Vespertilionidae

On following pages: 452. Long-toed Myotis (Myotis secundus); 453. Bornean Whiskered Myotis (Myotis borneoensis); 454. Malaysian Whiskered Myotis (Myotis federatus): 455. Indochinese Myotis (Myotis indochinensis); 456. Peyton's Myotis (Myotis peyton); 457. Burmese Whiskered Myotis (Myotis montivagus); 458. Long-fingered Myotis (Myotis capaccinii); 459. Chinese Water Myotis (Myotis laniger); 460. Csorba's Myotis (Myotis csorbal); 461. Kashmir Cave Myotis (Myotis longipes); 462. Annamit Myotis (Myotis annamiticus); 463. Phan Luong's Myotis (Myotis phanluongi); 464. Himalayan Whiskered Myotis (Myotis siligorensis); 465. Chestnut Myotis (Myotis badius); 466. Ridley's Myotis (Myotis ridley); 467. Thick-thumbed Myotis (Myotis rosseti); 468. Horsfield's Myotis (Myotis horsfieldi); 469. Pallid Large-footed Myotis (Myotis macrotarsus); 470. Stalker's Myotis (Myotis stalkeri); 471. Gray Large-footed Myotis (Myotis adversus); 472. Maluku Myotis (Myotis moluccarum); 473. Southern Myotis (Myotis macropus); 474. Lesser Large-footed Myotis (Myotis hasselti).

opennotspecifiedOct 2019View details →
zenodo32/100

On following pages: 368. Himalayan Broad-muzzled Bat (Submyotodon caliginosus); 369. Moupin Broad-muzzled Bat (Submyotodon moupinensis); 370. Northern Myotis (Myotis septentrionalis); 371. South-western Myotis (Myotis auriculus); 372. Western Small-footed Myotis (Myotis ciliolabrum); 373. Dark-nosed Small-footed Myotis (Myotis melanorhinus); 374. Eastern Small-footed Myotis (Myotis leibil); 375. California Myotis (Myotis californicus); 376. Little Brown Myotis (Myotis lucifugus); 377. Keen's Myotis (Myotis keenii); 378. Long-eared Myotis (Myotis evotis); 379. Fringed Myotis (Myotis thysanodes); 380. Arizona Myotis (Myotis occultus); 381. Longlegged Myotis (Myotis volans); 382. Flat-headed Myotis (Myotis planiceps); 383. Indiana Myotis (Myotis sodalis); 384. Cinnamon Myotis (Myotis fortidens); 385. Findley's Myotis (Myotis findley)); 386. Northern Hairy-legged Myotis (Myotis pilosatibialis); 387. Southern Hairy-legged Myotis (Myotis keaysi); 388. Red Myotis (Myotis ruber); 389. Riparian Myotis (Myotis riparius); 390. Velvety Myotis (Myotis simus); 391. Golden Myotis (Myotis midastactus); 392. Elegant Myotis (Myotis elegans); 393. Fish-eating Myotis (Myotis vives). in Vespertilionidae

On following pages: 368. Himalayan Broad-muzzled Bat (Submyotodon caliginosus); 369. Moupin Broad-muzzled Bat (Submyotodon moupinensis); 370. Northern Myotis (Myotis septentrionalis); 371. South-western Myotis (Myotis auriculus); 372. Western Small-footed Myotis (Myotis ciliolabrum); 373. Dark-nosed Small-footed Myotis (Myotis melanorhinus); 374. Eastern Small-footed Myotis (Myotis leibil); 375. California Myotis (Myotis californicus); 376. Little Brown Myotis (Myotis lucifugus); 377. Keen's Myotis (Myotis keenii); 378. Long-eared Myotis (Myotis evotis); 379. Fringed Myotis (Myotis thysanodes); 380. Arizona Myotis (Myotis occultus); 381. Longlegged Myotis (Myotis volans); 382. Flat-headed Myotis (Myotis planiceps); 383. Indiana Myotis (Myotis sodalis); 384. Cinnamon Myotis (Myotis fortidens); 385. Findley's Myotis (Myotis findley)); 386. Northern Hairy-legged Myotis (Myotis pilosatibialis); 387. Southern Hairy-legged Myotis (Myotis keaysi); 388. Red Myotis (Myotis ruber); 389. Riparian Myotis (Myotis riparius); 390. Velvety Myotis (Myotis simus); 391. Golden Myotis (Myotis midastactus); 392. Elegant Myotis (Myotis elegans); 393. Fish-eating Myotis (Myotis vives).

opennotspecifiedOct 2019View details →
zenodo32/100

On following pages: 97. Savi's Pipistrelle (Hypsugo savii); 98. Alashanian Pipistrelle (Hypsugo alaschanicus); 99. Cadorna's Pipistrelle (Hypsugo cadornae); 100. Joffre's Pipistrelle (Hypsugo joffrel); 101. Chinese Pipistrelle (Hypsugo pulveratus); 102. Chocolate Pipistrelle (Hypsugo affinis); 103. Pungent Pipistrelle (Hypsugo mordax); 104. Peters's Pipistrelle (Hypsugo peters); 105. Long-toothed Pipistrelle (Hypsugo dolichodon); 106. Burmese Pipistrelle (Hypsugo lophurus); 107. Red-brown Pipistrelle (Hypsugo kitcheneri); 108. Brown Pipistrelle (Hypsugo imbricatus); 109. Big-eared Pipistrelle (Hypsugo macrotis); 110. Vordermann's Pipistrelle (Hypsugo vordermanni), 111. Anchieta's Pipistrelle (Hypsugo anchieta); 112. Kirindy Pipistrelle (Hypsugo bemainty); 113. Mouse-like Pipistrelle (Hypsugo musciculus); 114. Broad-headed Pipistrelle (Hypsugo crassulus); 115. Eisentraut's Pipistrelle (Hypsugo eisentrautl); 116. Schlieffen's Bat (Nycticeinops schlieffenii); 117. Moloney's Mimic Bat (Mimetillus moloney)). in Vespertilionidae

On following pages: 97. Savi's Pipistrelle (Hypsugo savii); 98. Alashanian Pipistrelle (Hypsugo alaschanicus); 99. Cadorna's Pipistrelle (Hypsugo cadornae); 100. Joffre's Pipistrelle (Hypsugo joffrel); 101. Chinese Pipistrelle (Hypsugo pulveratus); 102. Chocolate Pipistrelle (Hypsugo affinis); 103. Pungent Pipistrelle (Hypsugo mordax); 104. Peters's Pipistrelle (Hypsugo peters); 105. Long-toothed Pipistrelle (Hypsugo dolichodon); 106. Burmese Pipistrelle (Hypsugo lophurus); 107. Red-brown Pipistrelle (Hypsugo kitcheneri); 108. Brown Pipistrelle (Hypsugo imbricatus); 109. Big-eared Pipistrelle (Hypsugo macrotis); 110. Vordermann's Pipistrelle (Hypsugo vordermanni), 111. Anchieta's Pipistrelle (Hypsugo anchieta); 112. Kirindy Pipistrelle (Hypsugo bemainty); 113. Mouse-like Pipistrelle (Hypsugo musciculus); 114. Broad-headed Pipistrelle (Hypsugo crassulus); 115. Eisentraut's Pipistrelle (Hypsugo eisentrautl); 116. Schlieffen's Bat (Nycticeinops schlieffenii); 117. Moloney's Mimic Bat (Mimetillus moloney)).

opennotspecifiedOct 2019View details →
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On following pages: 80. Corben's Long-eared Bat (Nyctophilus corbeni); 81. Pallid Long-eared Bat (Nyctophilus daedalus); 82. Gould's Long-eared Bat (Nyctophilus gould); 84. New Caledonian Long-eared Bat (Nyctophilus nebulosus); 85. Papuan Long-eared Bat (Nyctophilus microtis); 86. Pygmy Long-eared Bat (Nyctophilus walker); 87. Eastern Long-eared Bat (Nyctophilus bifax); 88. Northern Long-eared Bat (Nyctophilus arnhemensis); 89. Mount Missim Long-eared Bat (Nyctophilus shirleyae); 90. Small-toothed Long-eared Bat (Nyctophilus microdon); 91. Lesser Long-eared Bat (Nyctophilus geoffroyi); 92. Sunda Long-eared Bat (Nyctophilus heran); 93. Lord Howe Long-eared Bat (Nyctophilus howensis). in Vespertilionidae

On following pages: 80. Corben's Long-eared Bat (Nyctophilus corbeni); 81. Pallid Long-eared Bat (Nyctophilus daedalus); 82. Gould's Long-eared Bat (Nyctophilus gould); 84. New Caledonian Long-eared Bat (Nyctophilus nebulosus); 85. Papuan Long-eared Bat (Nyctophilus microtis); 86. Pygmy Long-eared Bat (Nyctophilus walker); 87. Eastern Long-eared Bat (Nyctophilus bifax); 88. Northern Long-eared Bat (Nyctophilus arnhemensis); 89. Mount Missim Long-eared Bat (Nyctophilus shirleyae); 90. Small-toothed Long-eared Bat (Nyctophilus microdon); 91. Lesser Long-eared Bat (Nyctophilus geoffroyi); 92. Sunda Long-eared Bat (Nyctophilus heran); 93. Lord Howe Long-eared Bat (Nyctophilus howensis).

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On following pages 51 Pygmy Bamboo Bat (Tylonyctens pygmaea). 52 Indoma ayan Lesser Bamboo Bat (Tylonycreııs fu/vrda). 53 Sunda Lesser Bamboo Bat (Tylonycrers pachypus) 54 Tonkm Greater Bamboo Bat (Tylonycrerıs ronk nensrs) 55 Malayan Greater Bamboo Bat (Ty onyctens malayana) 56 Sumatran Greater Bamboo Bat (Tyloııycrerıs robusta/a) 57 Yok Don He meted Bat (Cass srre us yokdonens s) 58 Surat He meted Bat (Cassısrrel us dımıssus), 59 Rohu s Bat (Phıleror brachyptems). 60 Western False Prp strelle (Fels srrellus mackenzıeı), 61 Eastern False P pıstrelle (Fa s stre us rasmanıens s) 62 Ye ow-I pped Cave Bat (Vespade us douglasorum). 63 Northern Cave Bat (Vespade us caunnus). 64 Fmleysons Cave Bat (Vaspadelus fınlaysonı), 65 Eastern Cave Bat (Vespade us rroughtonı) 66 In and Forest Bat (Vespade us bavsrstodrı) 67 Eastern Forest Bat (Vespadelus pumılus), 68 Lıttle Forest Bat (Vespade/us vu/turnus) 69 Large Forest Bat (Vespadelus der! ngtonı), 70 Southern Forest Bat (Vespade us ragu us) 71 Large-eared P ed Bet (Cha noobus dwyerr) 72 L tt e Pıed Bat (Cha/ınolobus pıcarus). 73 Hoary Wettled Bet (Che/rnolobus rııgrogrısaus), 74 Gould's Wattled Bat (Chalınolobus gouldıı). 75 New Caledonıan Wattled Bat (Chalıno/obus neocaledonıcus) 76 Chocolate Wattled Bet (Chalnolobus morro), 77 New Zealand Long-taıled Bat (Chahnolobus ruberculetus) in Vespertilionidae

On following pages 51 Pygmy Bamboo Bat (Tylonyctens pygmaea). 52 Indoma ayan Lesser Bamboo Bat (Tylonycreııs fu/vrda). 53 Sunda Lesser Bamboo Bat (Tylonycrers pachypus) 54 Tonkm Greater Bamboo Bat (Tylonycrerıs ronk nensrs) 55 Malayan Greater Bamboo Bat (Ty onyctens malayana) 56 Sumatran Greater Bamboo Bat (Tyloııycrerıs robusta/a) 57 Yok Don He meted Bat (Cass srre us yokdonens s) 58 Surat He meted Bat (Cassısrrel us dımıssus), 59 Rohu s Bat (Phıleror brachyptems). 60 Western False Prp strelle (Fels srrellus mackenzıeı), 61 Eastern False P pıstrelle (Fa s stre us rasmanıens s) 62 Ye ow-I pped Cave Bat (Vespade us douglasorum). 63 Northern Cave Bat (Vespade us caunnus). 64 Fmleysons Cave Bat (Vaspadelus fınlaysonı), 65 Eastern Cave Bat (Vespade us rroughtonı) 66 In and Forest Bat (Vespade us bavsrstodrı) 67 Eastern Forest Bat (Vespadelus pumılus), 68 Lıttle Forest Bat (Vespade/us vu/turnus) 69 Large Forest Bat (Vespadelus der! ngtonı), 70 Southern Forest Bat (Vespade us ragu us) 71 Large-eared P ed Bet (Cha noobus dwyerr) 72 L tt e Pıed Bat (Cha/ınolobus pıcarus). 73 Hoary Wettled Bet (Che/rnolobus rııgrogrısaus), 74 Gould's Wattled Bat (Chalınolobus gouldıı). 75 New Caledonıan Wattled Bat (Chalıno/obus neocaledonıcus) 76 Chocolate Wattled Bet (Chalnolobus morro), 77 New Zealand Long-taıled Bat (Chahnolobus ruberculetus)

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On following pages: 174. Small Big-eared Brown Bat (Histiotus montanus);, 175. Thomas's Big-eared Brown Bat (Histiotus laephotis); 176. Common Big-eared Brown Bat (Histiotus macrotus); 177. Southern Big-eared Brown Bat (Histiotus magellanicus); 178. Big Brown Bat (Eptesicus fuscus); 179. Guadeloupe Serotine (Eptesicus guadeloupensis); 180. Diminutive Serotine (Eptesicus diminutus); 181. Little Black Serotine (Eptesicus andinus); 182. Chiriguinan Serotine (Eptesicus chiriquinus); 183. Argentine Serotine (Eptesicus furinalis); 184. Harmless Serotine (Eptesicus innoxius); 185. Brazilian Serotine (Eptesicus brasiliensis); 186. Taddei's Serotine (Eptesicus taddeii); 187. Ulapes Serotine (Eptesicus ulapesensis); 188. Horn-skinned Serotine (Eptesicus floweri); 189. Lagos Serotine (Eptesicus platyops); 190. Long-tailed Serotine (Eptesicus hottentotus); 191. Ognev's Serotine (Eptesicus ognevi); 192. Anatolian Serotine (Eptesicus anatolicus); 193. Botta's Serotine (Eptesicus bottae); 194. Meridional Serotine (Eptesicus isabellinus); 195. Oriental Serotine (Eptesicus pachyomus); 196. Eurasian Serotine (Eptesicus serotinus); 197. Northern Serotine (Eptesicus nilssonil); 198. Sombre Serotine (Eptesicus tate); 199. Gobi Serotine (Eptesicus gobiensis), 200. Japanese Serotine (Eptesicus japonensis);, 201. Thick-eared Serotine (Eptesicus pachyotis). in Vespertilionidae

On following pages: 174. Small Big-eared Brown Bat (Histiotus montanus);, 175. Thomas's Big-eared Brown Bat (Histiotus laephotis); 176. Common Big-eared Brown Bat (Histiotus macrotus); 177. Southern Big-eared Brown Bat (Histiotus magellanicus); 178. Big Brown Bat (Eptesicus fuscus); 179. Guadeloupe Serotine (Eptesicus guadeloupensis); 180. Diminutive Serotine (Eptesicus diminutus); 181. Little Black Serotine (Eptesicus andinus); 182. Chiriguinan Serotine (Eptesicus chiriquinus); 183. Argentine Serotine (Eptesicus furinalis); 184. Harmless Serotine (Eptesicus innoxius); 185. Brazilian Serotine (Eptesicus brasiliensis); 186. Taddei's Serotine (Eptesicus taddeii); 187. Ulapes Serotine (Eptesicus ulapesensis); 188. Horn-skinned Serotine (Eptesicus floweri); 189. Lagos Serotine (Eptesicus platyops); 190. Long-tailed Serotine (Eptesicus hottentotus); 191. Ognev's Serotine (Eptesicus ognevi); 192. Anatolian Serotine (Eptesicus anatolicus); 193. Botta's Serotine (Eptesicus bottae); 194. Meridional Serotine (Eptesicus isabellinus); 195. Oriental Serotine (Eptesicus pachyomus); 196. Eurasian Serotine (Eptesicus serotinus); 197. Northern Serotine (Eptesicus nilssonil); 198. Sombre Serotine (Eptesicus tate); 199. Gobi Serotine (Eptesicus gobiensis), 200. Japanese Serotine (Eptesicus japonensis);, 201. Thick-eared Serotine (Eptesicus pachyotis).

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On following pages: 121. Roberts's Serotine (Neoromicia robertsi); 122. Stanley's Serotine (Neoromicia stanleyi); 123. Zulu Serotine (Neoromicia zuluensis): 124. Tiny Serotine (Neoromicia guineensis); 125. Somali Serotine (Neoromicia somalica); 126. Banana Serotine (Neoromicia nanus); 127. Rendall''s Serotine (Neoromicia rendall): 128. Dark-brown Serotine (Neoromicia brunnea); 129. Rosevear's Serotine (Neoromicia rosevear): 130. Isabelline Serotine (Neoromicia isabella); 131. Grandidier's Serotine (Neoromicia grandidieri); 132. White-winged Serotine (Neoromicia tenuipinnis); 133. Heller's Serotine (Neoromicia helios); 134. De Winton's Long-eared Bat (Laephotis wintoni); 135. Angolan Long-eared Bat (Laephotis angolensis); 136. Botswanan Long-eared Bat (Laephotis botswanae); 137. Namib Long-eared Bat (Laephotis namibensis): 138. Sind Bat (Rhyneptesicus nasutus); 139. Collared Sprite (Thainycteris aureocollaris); 140. Necklace Sprite (Thainycteris torquatus); 141. Bronze Sprite (Arielulus circumdatus); 142. Social Sprite (Arielulus societatis); 143. Coppery Sprite (Arielulus cuprosus). in Vespertilionidae

On following pages: 121. Roberts's Serotine (Neoromicia robertsi); 122. Stanley's Serotine (Neoromicia stanleyi); 123. Zulu Serotine (Neoromicia zuluensis): 124. Tiny Serotine (Neoromicia guineensis); 125. Somali Serotine (Neoromicia somalica); 126. Banana Serotine (Neoromicia nanus); 127. Rendall''s Serotine (Neoromicia rendall): 128. Dark-brown Serotine (Neoromicia brunnea); 129. Rosevear's Serotine (Neoromicia rosevear): 130. Isabelline Serotine (Neoromicia isabella); 131. Grandidier's Serotine (Neoromicia grandidieri); 132. White-winged Serotine (Neoromicia tenuipinnis); 133. Heller's Serotine (Neoromicia helios); 134. De Winton's Long-eared Bat (Laephotis wintoni); 135. Angolan Long-eared Bat (Laephotis angolensis); 136. Botswanan Long-eared Bat (Laephotis botswanae); 137. Namib Long-eared Bat (Laephotis namibensis): 138. Sind Bat (Rhyneptesicus nasutus); 139. Collared Sprite (Thainycteris aureocollaris); 140. Necklace Sprite (Thainycteris torquatus); 141. Bronze Sprite (Arielulus circumdatus); 142. Social Sprite (Arielulus societatis); 143. Coppery Sprite (Arielulus cuprosus).

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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.

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

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