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1,514 results for “Widespread”

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zenodo40/100

Figure 4 in Combined phylogenetic analysis of a new North American fossil species confirms widespread Eocene distribution for stem rollers (Aves, Coracii)

Figure 4. Cervical series, thoracic region, and sacrum of Paracoracias. Anatomical abbreviations: c, coracoid; cev, cervical vertebrae; f, frontal; fe, femur; fu, furcula; h, humerus; i, ischium; k, keel; lp, lateral process of sternum; p, pubis; r, radius; s, scapulae; sa, sacrum; u, ulna; up, uncinate processes.

opencc-by-4.0Oct 2009View details →
zenodo40/100

Figure 2 in Combined phylogenetic analysis of a new North American fossil species confirms widespread Eocene distribution for stem rollers (Aves, Coracii)

Figure 2. Holotype specimen of Paracoracias occidentalis (AMNH 30572). Anatomical abbreviations: II:1, manual phalanx II:1; cev, cervical vertebrae; cmc, carpometacarpus; cv, caudal vertebrae; f, frontal; fe, femur; h, humerus; k, keel; lp, lateral process of sternum; m, mandible; pe, pelvis; pmx, premaxilla; r, radius; s, scapulae; tbt, tibiotarsus; tmt, tarsometatarsus; u, ulna.

opencc-by-4.0Oct 2009View details →
zenodo40/100

Figure 5 in Combined phylogenetic analysis of a new North American fossil species confirms widespread Eocene distribution for stem rollers (Aves, Coracii)

Figure 5. Pectoral girdle and limbs of Paracoracias. Anatomical abbreviations: I:1, manual phalanx I:1; II:1, manual phalanx II:1; II:2, manual phalanx II:2; c, coracoid; cmc, carpometacarpus; fu, furcula; h, humerus; lp, lateral process of sternum; r, radius; s, scapulae; t, tracheal ring; tbt, tibiotarsus; u, ulna; ul, ulnare.

opencc-by-4.0Oct 2009View details →
zenodo40/100

Figure 3 in Combined phylogenetic analysis of a new North American fossil species confirms widespread Eocene distribution for stem rollers (Aves, Coracii)

Figure 3. Skull of Paracoracias. Anatomical abbreviations: cv, caudal vertebrae; f, frontal; hy, hyoid; j, jugal; l, lacrimal; m, mandible; na, naris; pal, palatine; pmx, premaxilla; por, postorbital process; pt, pterygoid; py, pygostyle; scl, sclerotic ring.

opencc-by-4.0Oct 2009View details →
zenodo40/100

Figure 7 in Combined phylogenetic analysis of a new North American fossil species confirms widespread Eocene distribution for stem rollers (Aves, Coracii)

Figure 7. Pelvic limb of Paracoracias in lateral view. Anatomical abbreviations: I:1, pedal phalanx I:1; II:1, pedal phalanx II:1; fb, fibula; fe, femur; h, humerus; tbt, tibiotarsus; tmt, tarsometatarsus; u, ulna.

opencc-by-4.0Oct 2009View details →
zenodo40/100

Figure 8 in Combined phylogenetic analysis of a new North American fossil species confirms widespread Eocene distribution for stem rollers (Aves, Coracii)

Figure 8. Strict consensus cladogram of two most parsimonious trees (length = 4882; consistency index = 0.424; retention index = 0.798; rescaled consistency index = 0.340) from the combined analysis using all morphological and sequence data (ND2, RAG-1, and c-myc). Bootstrap support values are presented above and Bremer support values are presented below the branch they refer to. Note that the crown clade Coracioidea (Coraciidae + Brachypteraciidae) is not labelled; the position of Geranopterus alatus with respect to this clade is unresolved. †, extinct taxa; NA, North American Coracii.

opencc-by-4.0Oct 2009View details →
zenodo40/100

Fig. 2 in Arganiella Giusti & Pezzoli, 1980 (Caenogastropoda: Truncatelloidea: Hydrobiidae): a widespread genus or several narrow-range endemic genera?

Fig. 2. Shells, operculum and radulae of Docleiana tabanensis (Boeters, Glöer & Pešić, 2014) (UGSB 18847). A–C. Shells. D–E. Operculum (D = inner side; E = outer side). F. Protoconch. G–I. Radulae. G. Portion of radula ribbon. H. Central radular teeth. I. Inner and outer marginal teeth.

opencc-by-4.0May 2021View details →
zenodo40/100

Fig. 1 in Arganiella Giusti & Pezzoli, 1980 (Caenogastropoda: Truncatelloidea: Hydrobiidae): a widespread genus or several narrow-range endemic genera?

Fig. 1. Maximum likelihood tree based on the combined (COI, 18S) dataset. Statistical support of the nodes is indicated when Bayesian posterior probabilities ≥ 0.95 and bootstrap supports ≥ 75% (black dots). On the right, the morphology of shell, penis and distal female genitalia is presented for: a) Arganiella wolfi Boeters & Glöer, b) A. pescei Giusti & Pezzoli, 1980 and c) A. tabanensis Boeters, Glöer & Pešić, 2014. Reproductive organs were re-drawn from Arconada & Ramos (2007a), Bodon et al. (2001) and Boeters et al. (2014) for the three species, respectively. Scale bar below topology: substitutions per site.

opencc-by-4.0May 2021View details →
zenodo40/100

Figure 1 in Systematics of a widespread Southeast Asian frog, Rana chalconota (Amphibia: Anura: Ranidae)

Figure 1. Map illustrating the provenance of specimens and tissues of the Rana chalconota species group used in this study. Squares represent specimens only, and circles represent both tissues and specimens.

opencc-by-4.0Jan 2009View details →
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Figure 2 in Systematics of a widespread Southeast Asian frog, Rana chalconota (Amphibia: Anura: Ranidae)

Figure 2. Fifty per cent majority-rule consensus phylogram resulting from mixed-model Bayesian analysis of mitochondrial DNA from frogs of the Rana chalconota species group. Trees were rooted with R. erythraea and R. nigrovittata (not shown). Numbers above and below nodes are Bayesian posterior probabilities and parsimony bootstrap values> 50, respectively. An asterisk (*) indicates a Bayesian posterior probability of 1.00 and parsimony bootstrap value of 100. Maximum parsimony analysis resolved the clades Peninsular Malaysia D [Peninsular Malaysia C (Thailand + Padang Small)], but without bootstrap support.

opencc-by-4.0Jan 2009View details →
zenodo40/100

Thermophilic methane oxidation is widespread in New Zealand geothermal fields

<p>This is processed data used for analysis in a manuscipt currently being prepared for publication.<br> Samples of soil or sediment were taken from geothermal fields in the Taupo Volcanic Zone, New Zealand;<br> methane oxidation was quantified; DNA was extracted from each sample for 16S rRNA gene sequencing.</p> <p>&nbsp;</p>

opencc-by-4.0Dec 2021View details →
zenodo40/100

NERC MSTRF Sky-Camera Time-Lapse Video for 2010-09-07 05:30 UTC (showing widespread development of Cumulonimbus clouds, some of which have extensive Anvils).

<p>A time-lapse video showing widespread development of Cumulonimbus clouds, some of which have extensive Anvils. A variety of other cumuloform clouds can be seen. The origin of the widespread cirrus cloud seen during the second half of the sequence is probably outflow from Cumulonimbus anvils. This video has been created from images taken by the NERC MST Radar Facility&#39;s Sky-Camera, which is located near Aberystwyth in West Wales. The images are freely available, under an Open (UK) Government License, from http://tinyurl.com/nerc-mstrf-sky-camera/ . For an explanation of the atmospheric phenomena that can be seen, download the resource available at http://cedadocs.ceda.ac.uk/1259/ .</p>

opencc-by-4.0Jul 2017View details →
dryad40/100

Genetic evidence for widespread population size expansion in North American boreal birds prior to the Last Glacial Maximum

<p>Pleistocene climate cycles are well known to have shaped contemporary species distributions and genetic diversity. Northward range expansions in response to deglaciation following the Last Glacial Maximum (LGM; ~21,000 years ago) have been surmised to lead to population size expansions in terrestrial taxa and changes in seasonal migratory behaviour. Recent findings, however, suggest that some northern temperate populations may have been more stable than expected through the LGM. We modelled the demographic history of twenty co-distributed boreal-breeding bird species of North America from full mitochondrial gene sets and species-specific molecular rates. We used these demographic reconstructions to test how species with different migratory strategies were affected by glacial cycles. Our results suggest that effective population sizes increased in response to deglaciation during the middle Wisconsin period (~45,000 years ago) whereas genetic diversity was maintained throughout the LGM despite shifts in geographic range. We conclude that earlier glacial cycles prior to the LGM have most strongly shaped contemporary genetic diversity in these high-latitude species. We did not find differences in historic population dynamics between species differing in migratory behaviour, contributing to growing evidence that major switches in migratory strategy during the Last Glacial Maximum are unnecessary to explain contemporary migratory patterns.</p>

opencc-zeroDec 2022View details →
dryad40/100

Data for: Widespread support for a global species list with a formal governance system

<p>This spreadsheet provides all cleaned and validated data used in the analysis of the GSLWG survey to gather opinions about the governance of taxonomic lists. Data are anonymous. Interpertations of variables are available in a separate codebook file, also available on Dryad and associated with this manuscript.</p> <p>In addition to raw survey data, additional supplemental data are provided:</p> <p>1. Coding manual providing definitions for each variable included in the survey dataset in .csv format</p> <p>2. The data analysis code in Stata .do format and PDF format</p> <p>3. The survey instrument in several languages in PDF format</p> <p>4. A detailed description of the survey methodology and data analysis approach in PDF format</p> <p>5. The full results of the survey in tabular form</p> <p>6. Additional figures presenting survey results</p> <p>All data are also available on the website of the Open Science Framework (OSF), along with survey pre-registration data: <a href="https://osf.io/tz7ra/?view_only=4b1bc810ef794f7f9bb57240611989af">https://osf.io/tz7ra/?view_only=4b1bc810ef794f7f9bb57240611989af</a></p>

opencc-zeroDec 2022View details →
dryad40/100

Widespread reticulate evolution in an adaptive radiation

<p>A fundamental assumption of evolutionary biology is that phylogeny follows a bifurcating process. However, hybrid speciation and introgression are becoming more widely documented in many groups. Hybrid inference studies have been historically limited to small sets of taxa, while exploration of the prevalence and trends of reticulation at deep time scales remains unexplored. We study the evolutionary history of an adaptive radiation of 109 gemsnakes in Madagascar (Pseudoxyrhophiinae) to identify potential instances of introgression. Using several network inference methods, we find twelve reticulation events within the 22-million-year evolutionary history of gemsnakes, producing 28% of the diversity for the group, including one reticulation that resulted in the diversification of an 18 species radiation. These reticulations occur at nodes with high gene tree discordance. Hybridization events occurred between north-south distributed parentals that share similar ecologies. Younger hybrids occupy intermediate contact zones between the parentals, showing that post-speciation dispersal in this group has not eroded the spatial signatures of introgression. Reticulations accumulated consistently over time, despite drops in overall speciation rates during the Pleistocene. This suggests that while bifurcating speciation may decline as the result of species accumulation and environmental change, speciation by hybridization may be more robust to these processes.</p>

opencc-zeroJan 2023View details →
zenodo40/100

Data for Widespread detection of chlorine oxyacids in the Arctic atmosphere: Villum Research Station and Ny-Ålesund observations

<p>The data includes:</p> <p>1) Data for the time series of HClO3 and HClO4&nbsp;together with relevant data&nbsp;from the Villum Research Station observations.</p> <p>2) Data for the time series of HClO3 from&nbsp;Ny-&Aring;lesund observation.</p> <p>3) Data of&nbsp;the estimated cross-section and photolysis rate of HClO3 and HClO4.</p> <p>Data are also available from the corresponding authors upon request.&nbsp;</p>

opencc-by-4.0Feb 2023View details →
zenodo40/100

FIG. 2 in Hygrophorus roseodiscoideus Bon & Chevassut: epitypification and updated biogeography of a poorly known but widespread thermophilous species

FIG. 2. — Macro- and microcharacters of the epitype of Hygrophorus roseodiscoideus Bon &amp; Chevassut. In situ photograph, violet hues are exaggerated as the photo has been taken with a flash. A, photo by P.-A. Moreau; B, pileipellis structure; C, lamellar trama structure; D, spore drawing; E, basidia drawing of PAM00103101 (LIP[LIP 0402283]). Scale bars: A, 1 cm; B, C, 100 µm; D, E, 10 µm.

opencc-zeroAug 2022View details →
zenodo40/100

FIG. 1 in Hygrophorus roseodiscoideus Bon & Chevassut: epitypification and updated biogeography of a poorly known but widespread thermophilous species

FIG. 1. — Original material of Hygrophorus roseodiscoideus Bon &amp; Chevassut: A, hand-written description sheet and color drawing of specimens of the holotype of H. roseodiscoideus by M. Bon; B, photograph of the dried basidiomata (holo-, Bon 84391 kept in LIP).

opencc-zeroAug 2022View details →
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FIG. 4 in Hygrophorus roseodiscoideus Bon & Chevassut: epitypification and updated biogeography of a poorly known but widespread thermophilous species

FIG. 4. — Basidiomata of Hygrophorus roseodiscoideus Bon &amp; Chevassut: A, Czech Republic, Čtvrtě, photo by J. Holec (PRM[PRM 955166]); B, Czech Republic, Sivický les, photo by D. Dvořák (BRNU[BRNU 677820]); C, France, Cucuron, photo by D. Borgarino (DiBo041202); D, Hungary, Mt. Széchenyi-hegy, photo by B. Dima (DB 2020-11-12-2); E, Italy, Cipresseta S. Agnese, photo by E. Campo (EC16102825); F, Italy, Passo Cantoniera, photo by A. Hausknecht (WU[WU-Myc 25200]). All collections were sequenced. For full collection data, see section Additionnal material examined.

opencc-zeroAug 2022View details →
zenodo40/100

Widespread changes in Southern Ocean phytoplankton blooms linked to climate drivers

<p>Bloom phenology metrics calculated from OC-CCI v6.0 data. Dataset forms part of a publication in Nature Climate Change.</p>

opencc-by-4.0Jun 2023View details →

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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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