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14,198 results for “14”
Figure 14 in On a small collection of Tetragonicipitidae Lang, 1944 (Copepoda: Harpacticoida) from Mexico: new records and new species
Figure 14. Phyllopodopsyllus parastigmosus sp. nov. Male. Antennule. Scale bar: 50 µm.
Figure 14 in Additions to the British list of Megaselia Rondani (Diptera: Phoridae), including two new species, from the crowns of ancient pollarded trees
Figure 14. Megaselia serrata female, details of abdomen, furca.
Rafue 14. Mooma Buinaima komuiya rafue baɨ zairikana jaaide
<p>Sal de vida, texto 14: Mooma Buinaima komuiya rafue baɨ zairikana jaaide (mp3 71 MB). Hablante: Oscar Romualdo Román Jitdutjaaño, lengua Murui Mɨnɨka (ISO hto). Lugar de grabación: Q. Aguasal, Colombia (0°32'50.62"S, 72°19'46.98"W). Fecha: Febrero 15 de 1998. Duración: 1:00:31. Transcripción disponible en: Ɨairue nagɨni: Aiñɨko urukɨ nagɨni, Aiñɨra urukɨ nagɨni = Halógeno-Halófita: Sal de vida, por Oscar Román-Jitdutjaaño, Simón Román y Juan Alvaro Echeverri (Leticia: Universidad Nacional de Colombia, Sede Amazonia, Instituto Amazónico de Investigaciones Imani, 2020, https://repositorio.unal.edu.co/handle/unal/77785), pp. 759-832</p>
FIG. 14 in Annotated checklist of the springtails (Hexapoda: Collembola) of the Collo massif, northeastern Algeria
FIG. 14. — Parisotoma notabilis (Schäffer, 1896). Body size: 0.8 mm.
Pure POPC membrane simulations using Amber Lipid 14 Force Field
<p>Pure POPC membrane simulations using the Amber Lipid 14 force field.</p> <pre>@article{dickson2014lipid14, title={Lipid14: the amber lipid force field}, author={Dickson, Callum J and Madej, Benjamin D and Skjevik, {\AA}ge A and Betz, Robin M and Teigen, Knut and Gould, Ian R and Walker, Ross C}, journal={Journal of chemical theory and computation}, volume={10}, number={2}, pages={865--879}, year={2014}, publisher={ACS Publications} }</pre> <p>The trajectories are centered such that the center of mass of the lipid tails are at the origin. <strong>Please check the imaging again to make sure that there are no problems. </strong></p> <p><strong>The trajectories do not contain water molecules.</strong> </p> <p>Simulation Details:</p> <p>Lipids : 72 POPC lipids, 36 per leaflet</p> <p>Water: 9560 TIP3P water molecules (<strong>water coordinates are not saved</strong>)</p> <p>Temperature: 303 K</p> <p>Pressure: 1 bar</p> <p>Thermostat: Langevin</p> <p>Barostat: Berendsen</p> <p>Pressure coupling: Semi-isotropic</p> <p>Trajectory Length: 100 ns (after 100 ns pre-equilibration)</p> <p>Saving frequency: 100 ps</p> <p>Further details are available at the 04_Run.in file</p> <p>All trajectories started from the same structure but equilibriated for 100 ns independently (using 03_Hold.in)</p>
Energetic Proton Propagation and Acceleration Simulated for the Bastille Day Event of July 14, 2000
<p>This includes data from the EPREM+CORHEL simulation run presented in "Energetic Proton Propagation and Acceleration Simulated for the Bastille Day Event of July 14, 2000" (Astrophysical Journal). The eight files ending in '.nc' contain the EPREM stream-observer data used to create Figures 5 & 7. The data was saved in the self-describing <a href="https://www.unidata.ucar.edu/software/netcdf/">NetCDF4</a> format. The HTML files contain the following interactive figures, which you can open in your internet browser:</p> <ul> <li><strong>cos_theta-e10.0-t44.html</strong> cosine of the flow angle (Figure 7)</li> <li><strong>divV-e10.0-t44.html</strong> velocity divergence (Figure 7)</li> <li><strong>flux-e10.0-t44-log.html</strong> differential flux of 10-MeV protons (Figure 7)</li> <li><strong>peak_flux-e10.0-t44.html</strong> relative peak flux of 10-MeV protons (Figure 5)</li> <li><strong>peak_flux-e100.0-t44.html</strong> relative peak flux of 100-MeV protons (not shown in paper)</li> <li><strong>tau_p-e10.0-t44-log.html</strong> theoretical acceleration rate (Figure 7)</li> </ul>
Strain fields in twisted bilayer graphene: Dataset 14 of 19
<p>See supplemental materials of Kazmierczak & Van Winkle et al for more information.</p> <p>02262020_26.h5 : dataset s1-26 corresponding to mean angle of 0.2609</p>
Figure 14 in Redescription of Bryobia pritchardi Rimando, 1962 (Acari: Tetranychidae), with an ontogeny of chaetotaxy
Figure 14 Bryobia pritchardi, deutonymph, ventral view. Scale bar 100 μm.
SRX3024507_bin_14
<p>Genome extracted by JORG.</p>
Images 14 & 15 in Description of a new species of scorpion of the genus Lychas C.L. Koch, 1845 (Scorpiones: Buthidae) from Maharashtra, India
Images 14 & 15. Lychas aareyensis sp. nov. female with juveniles (not collected)
Figure 14 in Morphology and life cycle of a new species of Psilocladus Blanchard, 1846 (Coleoptera, Lampyridae, Psilocladinae), the first known bromeliad-inhabiting firefly
Figure 14. Psilocladus costae sp. nov. Immature bioluminescence. (A) Larva (dorsal); (B) pupa (ventral). Length: larva = 18 mm; pupa = 7 mm.
Figures 14-19 in A generic key to the known larval Elmidae (Insecta: Coleoptera) of French Guiana
Figures 14-19. Larval habitus (dorsal, lateral, ventral). (14) Gyrelmis Hinton; (15) Hexacylloepus Hinton; (16) Neoelmis Musgrave; (17) Heterelmis Sharp; (18) Microcylloepus Hinton; (19) Macrelmis Motschulsky. Scale bars = 1 mm.
Data from: Fire catalyzed rapid ecological change in lowland coniferous forests of the Pacific Northwest over the past 14,000 years
Disturbance can catalyze rapid ecological change by causing widespread mortality and initiating successional pathways, and during times of climate change, disturbance may contribute to ecosystem state changes by initiating a new successional pathway. In the Pacific Northwest of North America (PNW), disturbance by wildfires strongly shapes the composition and structure of lowland forests, but understanding the role of fire over periods of climate change is challenging, because fire-return intervals are long (e.g., millennia) and the coniferous trees dominating these forests can live for many centuries. We developed stand-scale paleorecords of vegetation and fire that span nearly the past 14,000 yr to study how fire was associated with state changes and rapid dynamics in forest vegetation at the stand scale (1–3 ha). We studied forest history with sediment cores from small hollow sites in the Marckworth State Forest, located ~1 km apart in the Tsuga heterophylla Zone in the Puget Lowland ecoregion of western Washington, USA. The median rate of change in pollen/spore assemblages was similar between sites (0.12 and 0.14% per year), but at both sites, rates of change increased significantly following fire events (ranging up to 1% per year, with a median of 0.28 and 0.38%, P < 0.003). During times of low climate velocity, forest composition was resilient to fires, which initiated successional pathways leading back to the dominant vegetation type. In contrast, during times of high climate variability and velocity (e.g., the early Holocene) forests were not resilient to fires, which triggered large-scale state changes. These records provide clear evidence that disturbance, in the form of an individual fire event, can be an important catalyst for rapid state changes, accelerating vegetation shifts in response to large-scale climate change.
Figure 14 in Megalobulimus dryades, a new species from the Atlantic Forest in southeastern Brazil, and redescription of Megalobulimus gummatus (Gastropoda: Strophocheilidae)
Figure 14. Shells of Megalobulimus terrestris, M. oosomus and M. valenciennesii: (A-B) Megalobulimus terrestris MZSP 29322 (Agostina, PE), (A) apertural view, (B) abapertural view; (C-F) Megalobulimus oosomus, Holotype ANSP 32810 (Brazil), (C) apertural view, (D) lateral view, (E) abapertural view, (F) apical view; (G-H) Megalobulimus valenciennesii MZSP 28940 (Buerarema, BA), (G) apertural view, (H) abapertural view.
Cairn 14 in Sammallahdenmäki, Finland
Bronze age (from 1500 BC to 500 BC in Finland) burial cairn number 14 in Sammallahdenmäki, Rauma, Finland. There are total 36 tombs in the site. Sammallahdenmäki is [UNESCO World Heritage Site](https://whc.unesco.org/en/list/579). Other models from same site: * [Cairn 5 and 5A](https://skfb.ly/o6voK) * [Cairn 6, Huilun pitkä raunio ("long ruin of Huilu")](https://skfb.ly/o6v6U) * [Cairn 7](https://skfb.ly/o6vou) * [Cairn 10](https://skfb.ly/o6vpo) * [Cairn 11](https://skfb.ly/o6vov) * [Cairn 12](https://skfb.ly/o6voy) * [Cairn 20](https://skfb.ly/o6v6G) * [Cairn 21, Kinkonlaattia ("Church Floor") ](https://skfb.ly/o6v66) * [Cairn 22 and 23](https://skfb.ly/o6voF) * [Cairn 25 and 26](https://skfb.ly/o6v6y) * [Cairn 29 and 30](https://skfb.ly/o6voY) More info: * [Official Sammallahdenmäki website](https://www.sammallahdenmaki.fi/en/) * [Location in Google Maps](https://goo.gl/maps/jYyDirFcNPnKonPt8) * [Finnish Heritage Agency site info (only in finnish)](https://www.kyppi.fi/to.aspx?id=112.406010010) Source: Objaverse 1.0 / Sketchfab
Ullevi Gas Dilln 207 14 15
Ullevi, Gåsinge-Dillnäs 207:14-15 med flera, Södermanland. Hällristning med skeppsfigurer och skålgropar. Sörmlands museum och Opus Heritas. 3D-SFM. Source: Objaverse 1.0 / Sketchfab
COADS_14-78
Diagnostic biface collected in Liberty Township, Ross County, Ohio; Material: Delaware Uploaded by: Abby Clark Suggested Data Citation: Nolan, Kevin C., Andrew Weiland, Kelli Wathen, Abby Clark, and Michael Shott, 2017. COADS_14-78, 3D Model .ply file. Central Ohio Archaeological Digitization Survey, Department of Anthropology, University of Akron and Applied Anthropology Laboratories, Department of Anthropology, Ball State University. Source: Objaverse 1.0 / Sketchfab
2019-10 - Hangzhou 14
54 Photos taken with a Camera SONY Alpha 7 (RAW), then processed with Agisoft Photoscan Source: Objaverse 1.0 / Sketchfab
Newnan Point, SJ13_14
Newnan style biface, North Florida, Archaic (6200-5200 ya) Part of the Coontie Island Collection, SJ13_14 Model by Emily Jane Murray This model was made using RealityCapture software by Capturing Reality Source: Objaverse 1.0 / Sketchfab
Jarro - Fajalauza-HD (14)
Jarro (CE2037) producido en los talleres de Fajalauza (Granada, España). Ha sido modelado a torno y cocido en una atmósfera oxidante. Tiene una forma cerrada, parte de un labio redondeado y borde con orientación vertical que continúa en un cuello vertical y un hombro curvilíneo cóncavo. El cuerpo es globular y la base plana moldurada al exterior. Del cuerpo arranca un asa de puente con sección elíptica. Ha sido decorado en azul sobre fondo blanco con una composición floral central y carocas en el cuello. * Cronología: Siglo XVI. * Depósito: Museo Arqueológico y Etnológico de Granada. [FAJALAUZA-Hd](https://acortar.link/bNsUsm) Colaboran: [PRINMA](http://blogs.ugr.es/prinma/), [UGR](http://www.ugr.es), [Fundación Fajalauza](https://acortar.link/shJ8ps) , [Museo Arqueológico y Etnológico de Granada](https://acortar.link/DF0cOC), [Patronato de la Alhambra y Generalife](https://acortar.link/FcstHW) Fotografías y modelo: [Francisco Lara Piñera](https://acortar.link/Bam3Op) Source: Objaverse 1.0 / Sketchfab
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.