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2,441 results for “extinction”
The local extinction of Cedrus atlantica in the Iberian Peninsula could have been completed due to biological interaction
<p>This data set is used to explore the possibility that <em>Cedrus atlantica</em> (Endl.) Carrière and <em>Pinus nigra</em> Arnold could have interacted in the past, mutually excluding each other in the areas with suitable conditions for both species and, where, ultimately, the one that was most competitive would remain. The species show very well differenciated niches and a distribution of their habitats segregated by continents (<em>P. nigra</em> in Europe and <em>C. atlantica</em> in Africa), which responds to differences in climatic affinities. However, the contact of their distributions in bordering areas suggests that <em>C. atlantica</em> maintained its presence in the Iberian Peninsula until recent times, and that <em>P. nigra</em> could have displaced it due to its higher prevalence on the continent.</p>
Experimental data for "Deep Learning Methods for Colloidal Silver Nanoparticle Concentration and Size Distribution Determination from UV-Vis Extinction Spectra"
<p>Testing data (experimental data) for neural networks published in preprint https://doi.org/10.48550/arXiv.2404.10891</p> <p>The UV-VIS-NIR spectral data was also used in the dissertation of Nadzeya Khinevch, titled "Two-dimensional structures of nanoparticles for elements of surface-enhanced Raman scattering substrates".</p> <p>Emails of the corresponding authors:</p> <p>Tomas Klinavičius tomas.klinavicius@ktu.lt</p> <p>Tomas Tamulevičius tomas.tamulevicius@ktu.lt</p>
differential dust extinction towards SNR RX J1713.7-3946
<p>The dataset contains 6 approximate posterior sample of differential dust extinction towards the supernova remnant RX J1713.7-3946 .</p>
Replication data for "Climate change may induce connectivity loss and mountaintop extinction in Central American forests"
<p>Model code and predictor data underlying the publication "<strong>Climate change may induce connectivity loss and mountaintop extinction in Central American forests</strong>".</p>
Molecular and Taxonomic Reevaluation of the Digitaria filiformis Complex (Poaceae) including a Globally Extinct, Single Site Endemic from New Hampshire, USA, and a New Species from Mexico
<p>We examine the <em>Digitaria filiformis </em>complex, to determine the proper taxonomic rank and rarity of each taxon. The taxonomy of the <em>D. filiformis </em>complex is highly debated and includes two widespread species, <em>D. filiformis </em>and <em>D. villosa</em>; a possibly extinct species endemic to a single-site in New Hampshire, <em>D. laeviglumis</em>; and a rare species of southern Florida and the West Indies, <em>D.</em><em> dolichophylla. </em>We conducted morphologic comparisons and molecular analysis of the four members of the <em>D. filiformis</em> complex, together with specimens from Mexico and Venezuela purportedly identified as <em>D. laeviglumis</em> (morphology only). Based on results of phylogenetic analyses of plastid and nuclear ITS sequences and morphologic comparisons, we recognize five species in the <em>D. filiformis </em>complex, including a newly described Mexican endemic <em>D. glabrifloris. </em>After field investigation we have moved the global rank of <em>D. laeviglumis </em>from globally historical (GH) to extinct (GX), as there is virtually no likelihood of rediscovery. <em>Digitaria</em><em> dolichophylla </em>is much rarer than previously recognized, moving from secure (T5) to imperiled with extinction (G2).</p>
North Temperate Lakes LTER: Light Extinction 1981 - current
A light (PAR) extinction coefficient is calculated for the water column for the eleven primary lakes (Allequash, Big Muskellunge, Crystal, Sparkling, Trout, Crystal Bog, Trout Bog, Mendota, Monona, Wingra, and Fish) and two additional lakes near Madison, Wisconsin (Waubesa and Kegonsa). Data exists only for the Trout Lake-area lakes through 2018. Beginning in 2019, the Madison-area lakes were added. The fraction of surface light is computed at 0.25-m to 1-m depth intervals depending on the lake. The light (PAR) extinction coefficient is calculated by regressing ln(fraction of light(z)) on depth z. Sampling Frequency: fortnightly during ice-free season - every 6 weeks during ice-covered season Number of sites: 13. The raw light data can be found in two other datasets: https://portal.edirepository.org/nis/mapbrowse?scope=knb-lter-ntl&identifier=29 & https://portal.edirepository.org/nis/mapbrowse?scope=knb-lter-ntl&identifier=401
Mutual extinction and transparency of multiple incident light waves
<p>The basic publication is:<br> A. Lagendijk, A.P. Mosk, and W.L. Vos<br> Europhys. Lett., 130, 34002 (2020)<br> "Mutual extinction and transparency of<br> multiple incident light waves"<br> <br> We have uploaded to the Zenodo database all data enabling everyone to reuse our data, and<br> to reproduce all the figures of our paper</p> <p>The upload contains the file "readme.txt" explaining the content of the upload</p>
Supplementary material for "A drop in immigration results in the extinction of a local woodchat shrike population"
<p>Data files and code for all analyses and figures presented in the paper. The three data files are provided either in ASCII format (WoodchatCount.txt, WoodchatReproduction.txt, WoodchatCMR.txt) or in csv format (WoodchatCount.csv, WoodchatReproduction.csv, WoodchatCMR.csv). The code file (WoodchatCode.txt) is a space delineated text file. The code file is written for R, but some models are run in JAGS from R. The code file also contains the description of the data files and code for data management.</p>
OMPS-NPP L2 LP USask Aerosol Extinction Vertical Profile swath daily V1.1
<p>The USask OMPS-LP L2 2D Aerosol v1.1 product provides stratospheric aerosol extinction retrievals performed at the University of Saskatchewan for the central slit of the Ozone Mapping and Profiler Suite Limb Profiler (OMPS-LP) instrument on the Suomi-NPP satellite. The two-dimensional retrieval algorithm accounts for variation in the along orbital track dimension, retrieving an entire orbit simultaneously instead of treating each image independently. Stratospheric aerosol is retrieved from approximately the thermal tropopause to 30 km on a 1 km grid with a vertical resolution of approximately 2 km, and is assumed to be sulfate aerosol following a log-normal particle size distribution.</p> <p>Each granule contains data from the daylight portion of each orbit measured for a full month. Spatial coverage is global (-82 to +82 degrees latitude), and there are about 14.5 orbits per day, each has typically 160 profiles with an along orbital track sampling of 125 km. The files are written using NetCDF4.</p>
Mammals under pressure: presence data for assessing extinction of endemic, threatened, and mammals subject to use, in Colombia
<p>This is the first dataset that provides a complete compilation of mammal records based on camera traps, human observations, and specimens deposited in biological collections in Colombia. We compiled a dataset with unpublished information, including 97,943 records corresponding to 136 species, of which 38 are endemic, 92 are identified as species subject to use by humans in the literature, and 33 are categorized either as Data Deficient or threatened according to international or unofficial national assessments. The information comes from 31 out of 32 departments of Colombia and constitutes relevant input for future distribution and conservation assessments. Most records (n=96,417, 98.44%) come from non-invasive sampling methods such as camera traps. However, we highlight the contribution of museum specimens (n= 1,332), especially for small and medium-sized species, many of them with restricted distributions in the country. This dataset constitutes a joint collaborative and interinstitutional effort that serves as the basis for cooperative work to comprehensively assess the current conservation status of all mammal species in Colombia.</p>
Species diversity and extinction risk of vertebrate pollinators in India
<p>This repository includes the data compiled and used for the study of <strong>‘Species diversity and extinction risk of vertebrate</strong><br><strong>pollinators in India’</strong>. If you use these data, please cite them along with our manuscript:</p> <blockquote> <p>Kallivalappil R., Grattarola F., de Alwis Pitts D., Cotter S.C. & Pincheira-Donoso D. (2024). Species diversity and extinction risk of vertebrate<br>pollinators in India. <em>Biodiversity and Conservation</em>. https://doi.org/10.1007/s10531-024-02848-3</p> </blockquote> <p> </p> <h2>Abstract</h2> <p>Animal pollinators underpin the functioning and persistence of ecosystems globally. However, the vital role of pollination is being progressively eroded by the worldwide decline of pollinator species caused by human-induced environmental degradation, resulting in rising costs to biodiversity, agriculture, and economy. Most studies quantifying pollinator diversity and declines have focused on insects, whereas vertebrate pollinators remain comparatively neglected. Here, we<br>present the first comprehensive study quantifying the macroecological patterns of species richness and extinction risk of bird and mammal pollinators in India, a region of extremely high biodiversity and increasing anthropogenic pressure. Our results reveal that hotspots of mammal pollinator diversity are restricted to the south of the Western Ghats, whereas bird pollinator diversity hotspots are scattered throughout the country. Analyses of hotspots of threatened species<br>(based on the IUCN Red List) show that only mammal pollinators are currently classified as threatened in India, whereas multiple hotspots of population declines were observed for birds, and primarily in the Southwest for mammal pollinators. Our analyses failed to identify a role for species traits as drivers of these patterns, whereas most pollinators appear to be threatened by agriculture, logging and hunting for food, and medicinal purposes. Pollinator endangerment has widescale<br>ecological and economic implications such as reduced food production, plant extinction, loss of functional and genetic diversity, and economic damage. We suggest protection of vertebrate pollinators should be emphasised in active conservation agendas in India.</p> <p> </p> <h2>Files</h2> <h3>Spatial</h3> <ul> <li><code>india.gpkg</code></li> <li><code>birds.gpkg</code></li> <li><code>mammals.gpkg</code></li> <li><code>how_to_read_gpkg_data.R</code></li> </ul> <h3>Phylogenetic</h3> <ul> <li><code>PGLS_phylogeny_birds.nex</code></li> <li><code>PGLS_phylogeny_mammals.nex</code></li> </ul> <h3>Tables</h3> <ul> <li><code>all_bird_traits.csv</code></li> <li><code>all_mammals_traits.csv</code></li> <li><code>threatened_mammals_traits.csv</code></li> <li><code>plant_pollinator_dataset.csv</code></li> <li><code>pollinator_plant_dataset.csv</code></li> <li><code>references.txt</code></li> </ul>
Effects of intolerance of uncertainty on subjective and psychophysiological measures during threat acquisition and delayed threat extinction
<p>This dataset includes measurements of intolerance of uncertainty (Intolerance of Uncertainty Scale [Freeston et al., 1994]), trait anxiety (State-Trait Anxiety Inventory [Spielberger et al., 1983]), skin conductance response (SCR), fear potentiated startle (FPS) and fear ratings (RAT) acquired in a differential fear conditioning paradigm with habituation and threat acquisition training on one day and extinction training, mood induction (by presenting negative vs. neutral slides), re-extinction training, reinstatement and reinstatement-test 24h later. Overall, 66 participants (female = 44, aged between 18 and 40 years, M = 25.76, SD = 5.82) took part in the study. Several participants had to be excluded due to technical issues (n = 3), non-responding (SCR: n = 2; auditory startle blink: n = 1) and no SCRs to the CSs (n = 1). Visual CSs were two shapes resembling snowflakes. The US consisted of a train of three 2 ms electrotactile square-waves (inter stimulus interval, ISI: 50 ms) and was delivered 7.9 s after each CS+ onset (100% reinforcement rate) during threat acquisition training and three times during reinstatement. The duration of the ITIs ranged from 10 to 13 s (M = 11.5). For SCR measurements, a 1 Hz lowpass filter and a gain of 5 or 10 μΩ were applied. SCR data were scored by using the semi-automatic scoring system Autonomate (Green et al., 2014), down sampled to 10 Hz and scored as the first response within 0.9 to 4 s after CS onset as SCR from trough to peak with a maximum rise time of 5 s. SCRs were square root transformed to reduce skew and z-scored within individuals across trials for day 1 and day 2 separately. To elicit the auditory startle blink, a 95 dB white noise burst was presented simultaneously on both ears. Startle probes were administered 6 or 8 s after the ITI-onset and 6 or 7 s after CS-onset. A gain of 5000 at 1000 Hz and a band-pass filter (28–500 Hz) were applied. Data were rectified and integrated online (averaged over 20 samples) and scored semi-automatically by using a custom-made computer program (EDA View, developed by Prof. Dr. Matthias Gamer, University of Würzburg) as trough to peak 20–120 ms after startle probe onset. For analyses, FPS data was z-scored within individuals across trials for day 1 and day 2 separately. To acquire fear ratings, participants rated throughout the experiment, how much stress, fear, and tension they experienced, when they last saw the CSs. Answers had to be logged in via button press within 7 s on a visual analog scale (VAS) ranging from zero (answer = none) to 100 (answer = maximum). Unlogged ratings were considered as missing values.</p>
Data from: The legacy of the extinct Neotropical megafauna on plants and biomes
<p>The main dataset consists of ecoregion-level data on five plant functional traits (wood density, leaf size, stem spines, leaf spines and latex production), as well as ecoregion-level data on extinct megafauna historical patterns, fire, climate, soil, hurricanes and geografical variables (first spreadsheet) for the Neotropical biogeographic realm (Table 1). It also includes species-level plant functional trait data, and the abundance (presence-absence for leaf size) of these species, and the occurrences extinct megafauna and extant mammal herbivore species per Neotropical ecoregion, as well as diet data compiled for megafauna species. The species-level functional trait data was compiled from the literature and the names of the species in these data was used to search for occurrence data for these species in the Global Biodiversity Information Facility (Data available from GBIF using the following doi: WD: 10.15468/dl.3vua3x; Stem spines: 10.15468/dl.ar5ddj; Latex: 10.15468/dl.m8dzjd; Leaf spines: 10.15468/dl.vv8gw4; Leaf size: 10.15468/dl.k98nxc). During the process, species level were corrected and updated using tools from the "rgbif" package for R. We then croped only the Neotropical region, and calculate ecoregion level trait means for continuous traits (Wood Density and Leaf Size) and maximum por binary traits (Stem and Leaf Spines, Latex), using the ecoregion shapefile provided in https://storage.googleapis.com/teow2016/Ecoregions2017.zip. We obtained data on historical distribution of megafauna species and extant mammal species from the MegaPast2Future/PHYLACINE_1.2 dataset, and obtained diet information from literature sources. Climate data was obtained from WorldClim 2.1 (10 minute spatial resolution) and was based on climate data from 1970 and 2000. Soil data were obtained from SoilGrids (5 km of spatial resolution), and consisted of mean values for two depths, 0.05 and 2 m. We obtained the number (a proxy for frequency) and intensity of wildfires per ecoregion area using the MODIS active fire location product (MCD14ML). We only considered fires with detection confidence of 95% or higher occurring from November 2000 to December 2019 (both included). To ensure that only wildfires were considered, we associated each fire pixel with a land cover type (300 m of spatial resolution) from for a buffer area of 1000 m surrounding the fire pixel centroid. We excluded all of the fires occurring in areas in which more than 10% of the surrounding land cover pixels corresponded to agricultural, urban and water classes. We calculated the number of wildfires per ecoregion area by dividing the fire count of each Ecoregion by the ecoregion area, and multiplying the resulting value by the proportion of vegetated land cover pixels (same classes used to exclude fires in anthropogenic areas and water bodies above). Fire intensity was estimated as the average fire radiative power across all detected wildfires in the ecoregion. We also classified ecoregions into insular (1), when most of the ecoregion area was located in islands, vs. continental (0), otherwise. We also compiled data on hurricane activity, as woody density was suggested to confer resistance against this disturbance. We used data from 1990 to 2019 from the HURDAT2 dataset, containing six-hourly information about the location of all of the known tropical and subtropical cyclones (0.1° latitude/longitude). We used the sum of hurricane occurrences per ecoregions divided by ecoregion area as an indicator of hurricane activity.</p> <p>Three .txt files containing the custom codes developed for building the Ecoregion-level dataset (predictors and traits) and for data analyses used in the article are also included.</p>
Data for article: A quantitative framework to infer the effect of traits, diversity and environment on dispersal and extinction rates from fossils
<p>Supplementary information for:</p> <p><strong>A quantitative framework to infer the effect of traits, diversity and environment on dispersal and extinction rates from fossils</strong></p> <p>Torsten Hauffe, Mathias M. Pires, Tiago B. Quental, Thomas Wilke, and Daniele Silvestro</p> <p> </p><ul> <li> Simulations <ul> <li>Scripts <ul> <li>Scenario1_SamplingHeterogeneity.R: Script to simulate biogeographic histories with sampling heterogeneity</li> <li>Scenario3_SealevelInvasion.R: Script to simulate biogeographic histories where sea level facilitates dispersal and invasion induces extinction</li> <li>Scenario3_DiversityDependence.R: Script to simulate diversity-dependent biogeographic histories</li> <li>Scenario4_TraitDependence.R: Script to simulate trait-dependent biogeographic histories</li> <li>Scenario5_CategoricalTraitDependence.R: Script to simulate trait-dependent biogeographic histories</li> </ul> </li> <li>Results <ul> <li>Scenario1_SamplingHeterogenetiy_alpha05.txt: Results of simulations scenario 1 with a sampling heterogeneity of alpha = 0.5</li> <li>Scenario1_SamplingHeterogenetiy_alpha1.txt: Results of simulations scenario 1 with a sampling heterogeneity of alpha = 1</li> <li>Scenario1_SamplingHeterogenetiy_alpha2.txt: Results of simulations scenario 1 with a sampling heterogeneity of alpha = 2</li> <li>Scenario1_SamplingHeterogenetiy_alpha10.txt: Results of simulations scenario 1 with a sampling heterogeneity of alpha = 10</li> <li>Scenario2_Independent_dispersal_and_extinction.txt: Results of simulation scenario 2 with sea-level independent dispersal and no invasion induced extinction</li> <li>Scenario2_Sealevel_dependent_dispersal_and_independent_extinction.txt: Results of simulation scenario 2 with sea-level dependent dispersal and no invasion induced extinction</li> <li>Scenario2_Sealevel_independent_dispersal_and_invasion_induced_extinction.txt: Results of simulation scenario 2 with sea-level independent dispersal and invasion induced extinction</li> <li>Scenario2_Sealevel_dependent_dispersal_and_invasion_induced_extinction.txt: Results of simulation scenario 2 with sea-level dependent dispersal and invasion induced extinction</li> <li>Scenario3_Independent_dispersal_and_extinction.txt: Results of simulations scenario 3 with diversity-independent dispersal and extinction</li> <li>Scenario3_Diversity_dependent_dispersal_and_independent_extinction.txt: Results of simulations scenario 3 with diversity-dependent dispersal and diversity-independent extinction</li> <li>Scenario3_Independent_dispersal_and_Diversity_dependent_extinction.txt: Results of simulations scenario 3 with diversity-dependent dispersal and diversity-independent extinction</li> <li>Scenario3_Diversity_dependent_dispersal_and_extinction.txt: Results of simulations scenario 3 with diversity-dependent dispersal and extinction</li> <li>Scenario4_Independent_dispersal_and_extinction.txt: Results of scenario 4 with trait-independent dispersal and extinction</li> <li>Scenario4_Trait_dependent_dispersal_and_independent_extinction.txt: Results of scenario 4 with trait-dependent dispersal and independent extinction</li> <li>Scenario4_Independent_dispersal_and_trait_dependent_extinction.txt: Results of scenario 4 with independent dispersal and trait-dependent extinction</li> <li>Scenario4_trait_dependent_dispersal_and_extinction.txt: Results of scenario 4 with trait-dependent dispersal and extinction</li> <li>Scenario5_CatTrait_dependent_dispersal_and_independent_extinction.txt: Results of model 2 with categorical traits (e.g family) influence dispersal but no influence of a category-specific continuous traits</li> </ul> </li> </ul> </li> <li>Carnivora <ul> <li>BinnedOccurrence: Folder with 100 replicates of binned occurrences of max. 330 carnivoran genera throughout the Neogene</li> <li>BodyMass: Folder with 100 replicates of body mass for 330 carnivoran genera</li> <li>Sealevel: Folder with sea level through the Neogene</li> <li>Temperature: Folder with the temperature record of the Neogene</li> <li>Families: Folder with families as taxonomic proxy for phylogeny. FamilyGeneraNumeric.txt is the numeric coding used for the Bayesian analyses of carnivoran biogeography</li> </ul> </li> </ul> <p></p>
The Identification of Extinct Megafauna in Rock art Using Geometric Morphometrics: A Genyornis newtoni Painting in Arnhem Land, Northern Australia?
<p>Raw data files used for the analysis of a contentiously identified rock-art image located in Arnhem Land, Northern Australia. The data were used to test a novel approach to quantifying species identification in rock art images to assess the extent to which an image resembles other rock art of sound identification or anatomical images of visually similar species.</p> <p>Included files are the raw coordinate data files ("[feature] PCA file", .txt format) for use in Morphologika2, and formatted files for use in CVAGen8 ("[feature]" x1y1 file for CVA", .x1y1 format; "[feature] group file", .txt format).</p> <p>Files produced using software by Rohlf (2015) and Sheets (2014)</p>
Coping with Collapse: Functional Robustness of Coral-Reef Fish Network to Simulated Cascade Extinction
<p>Data set, codes and results related to the article "Coping with Collapse: Functional Robustness of Coral-Reef Fish Network to Simulated Cascade Extinction", accepted in the periodic Global Change Biology. Stored are the full results of site occupancy models fitted to fish data, with coral and turf algae cover as predictor variables (results published in Luza et al. 2022, Scientific Reports), and the results of the present article. The RData also contains site coordinates, and the fish traits used in trait-based analyzes.</p>
Extinction Rebellion Netherlands: Dutch Climate Activism Tweets (2020-2023)
<p>This dataset contains text data from Extinction Rebellion Netherlands (XR NL) tweets between January 1, 2020, and December 31, 2023. It captures key moments in the Dutch climate activism movement, focusing on themes such as environmental protests, fossil fuel resistance, and civil disobedience. The tweets reflect XR NL’s efforts in organizing non-violent direct actions and blockades, including significant events like the A12 highway protests and Schiphol airport demonstrations. Central themes include the climate crisis, sustainability, and the ecological emergency, highlighting the movement’s focus on climate justice and the call for urgent government action in the Netherlands.</p>
Supplementary Data for "Climate change may induce connectivity loss and mountaintop extinction in Central American forests"
<p>Supplementary data underlying the main figures presented in the publication "<strong>Climate change may induce connectivity loss and mountaintop extinction in Central American forests</strong>"</p>
Morphological cladogenesis and terminal dwarfing in extinct Late Miocene through Pliocene menardiform globorotalids: New complementary data to «Evolutionary prospection in the Neogene planktic foraminifer Globorotalia menardii and related forms from ODP Hole 925B (Céara Rise, western tropical Atlantic): evidence for gradual evolution superimposed by long distance dispersal ?, Swiss J. Palaeontology, 135:205-248»
<p>A complementary morphometric data set is provided to the study of Knappertsbusch (2016) about the shell evolution of menardiform globorotalids (Neogene planktic foraminifera) at ODP Hole 925B from Céara Rise in the the western tropical Atlantic. The new measurements confirm splitting of extinct <em>Globorotalia multicamerata</em> from the <em>G. menardii</em> stock via the intermediate form <em>G. limbata</em> between about 6 Ma to 5 Ma ago. After splitting both <em>G. limbata</em> and <em>G. multicamerata</em> show gradual divergence from <em>G. menardii</em> in several shell parameters illustrating morphological cladogenesis. Between 2.88 Ma and 2.59 Ma the same parameters show a concerted trend towards reduced values indicating pre-extinction dwarfing. A comparison with published literature data of Delta<sup>18</sup>O trends between species, that populated the mixed layer (<em>Globigerinoides sacculifer</em>) and the thermocline layer (<em>Neogloboquadrina dutertrei</em>) at this location during those times suggests, that both divergence and subsequent dwarfing trends were probably the results of changes in upper watermass stratification.</p> <p>The complementary data set is provided in six zipped archives APPENDIX A, B, C, D, E and F (zipped with free software 7-Zip 22.00 (x64), 2022-06-15 from 1999-2022 Igor Pawlow), together with a description of the data in file Report_925B_suppl_1.pdf.</p>
Supplementary Files for "Extinction debt and functional traits mediate community saturation over large spatiotemporal scales"
<p><strong>Supplementary Files for "Extinction debt and functional traits mediate community saturation over large spatiotemporal scales"</strong></p> <p><strong>Supplementary Tables:</strong></p> <p><strong>Supplementary Table S1.</strong> Species composition data of the 67 sites included herein from members of the Dipsadidae.</p> <p><strong>Supplementary Table S2.</strong> Scores for the Principal Component (PC) Axes corresponding to the PC analyses performed with the climatic variables of the sites included in this work.</p> <p><strong>Supplementary Table S3.</strong> Species composition data of the 67 sites included herein from species from families different from Dipsadidae.</p> <p><strong>Supplementary Table S4.</strong> Functional data corresponding to each of the species found in the 67 sites included in this work.</p> <p><strong>Supplementary Table S5.</strong> Functional data corresponding to each of the species from families different from Dipsadidae found in the 67 sites included in this work.</p> <p><strong>Supplementary Table S6.</strong> GenBank accession numbers of each of the sequences used for constructing the timetree used for this work.</p> <p><strong>Supplementary Table S7.</strong> Table indicating the areas inhabited by each of the species of the Dipsadidae included in the Bayesian timetree used for the ancestral area estimation performed herein.</p> <p><strong>References used for constructing Supplementary Tables S4 and S5</strong></p> <p> </p> <p><strong>Supplementary Figures:</strong></p> <p><strong>Supplementary Figure S1.</strong> Results of the ancestral estimations as recovered by ‘BioGeoBEARS’</p>
ScienceDex guides
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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.