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1,291 results for “gap”
Ar (750.4 nm) and OH free radical (309 nm) change along the discharge gap intensity (microwave frequency 2.45 GHz, flow 3 L/min input power 70W and 100W, respectively).
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Linked collectors and determiners for: Filling the gaps: descriptions of unnamed species included in the latest molecular phylogeny of Pholcidae (Araneae).
Natural history specimen data linked to collectors and determiners held within, "Filling the gaps: descriptions of unnamed species included in the latest molecular phylogeny of Pholcidae (Araneae)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/aa93de4b-c9ed-4b3e-a1c2-3f5d90faba57">https://bionomia.net/dataset/aa93de4b-c9ed-4b3e-a1c2-3f5d90faba57</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/aa93de4b-c9ed-4b3e-a1c2-3f5d90faba57">https://gbif.org/dataset/aa93de4b-c9ed-4b3e-a1c2-3f5d90faba57</a>. Formatted as a Frictionless Data package.
Axion gap production - output ray-tracer (part 1)
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Cartoon: Achieving NetZero: Evaluating interventions to reduce carbon-emissions on the patient care pathway in secondary healthcare - A systematic review and evidence gap map
<p>These three cartoons provide a summary of findings from the systematic review entitled: "Effectiveness of interventions to reduce carbon-emissions within secondary healthcare: Systematic review and narrative synthesis.</p> <p>For further detail on the background, main results and recommendations arising from this systematic review, we recommend you consult the Full Repor and/or Briefing Paper linked below.</p> <p>This work is carried out by Exeter Policy Research Programme Evidence Review Facility [NIHR 200695]. Views expressed are those of the authors and not necessarily those of the NHS, NIHR, Greener NHS team or NHS England.</p> <p> </p> <p> </p>
FORAlign: Accelerating gap-affine DNA pairwise sequence alignment using FOR-blocks based on FOur Russians approach with linear space complexity
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Data from: Mind the gap: genetic manipulation of basicranial growth within synchondroses modulates calvarial and facial shape in mice through epigenetic interactions
Phenotypic integration patterns in the mammalian skull have long been a focus of intense interest as a result of their suspected influence on the trajectory of hominid evolution. Here we test the hypothesis that perturbation of cartilage growth, which directly affects only the chondrocranium during development, will produce coordinated shape changes in the adult calvarium and face regardless of mechanism. Using two murine models of cartilage undergrowth that target two very different mechanisms, we show that strong reduction in cartilage growth produces a short, wide, and more flexed cranial base. This in turn produces a short, wide face in both models. Cranial base and face are already correlated early in ontogeny, and the relationship between these modules gains structure through postnatal growth and development. These results provide further evidence that there exist physical interactions between developing parts of the phenotype that produce variation at a distance from the actual locus upon which a particular selective pressure is acting. Phenotypic changes observed over the course of evolution may not all require adaptationist explanations; rather, it is likely that a substantial portion of observed phenotypic variation over the history of a clade is not directly adaptive but rather a secondary consequence of some local response to selection.
FIGURE 3 in Patterns of diversity and gaps in vascular (hemi-)epiphyte flora of Southwestern Amazonia
FIGURE 3. Collecting density of epiphytes by municipality in Acre.
Supplementary material 3 from: Haubrock PJ, Cuthbert RN, Yeo DCJ, Banerjee AK, Liu C, Diagne C, Courchamp F (2021) Biological invasions in Singapore and Southeast Asia: data gaps fail to mask potentially massive economic costs. In: Zenni RD, McDermott S, García-Berthou E, Essl F (Eds) The economic costs of biological invasions around the world. NeoBiota 67: 131-152. https://doi.org/10.3897/neobiota.67.64560
Annual average costs of biological invasions in Singapore. Note the y-axis is on a log10 scale
Supplementary material 2 from: Haubrock PJ, Cuthbert RN, Yeo DCJ, Banerjee AK, Liu C, Diagne C, Courchamp F (2021) Biological invasions in Singapore and Southeast Asia: data gaps fail to mask potentially massive economic costs. In: Zenni RD, McDermott S, García-Berthou E, Essl F (Eds) The economic costs of biological invasions around the world. NeoBiota 67: 131-152. https://doi.org/10.3897/neobiota.67.64560
Database subset
Supplementary material 4 from: Renault D, Manfrini E, Leroy B, Diagne C, Ballesteros-Mejia L, Angulo E, Courchamp F (2021) Biological invasions in France: Alarming costs and even more alarming knowledge gaps. In: Zenni RD, McDermott S, García-Berthou E, Essl F (Eds) The economic costs of biological invasions around the world. NeoBiota 67: 191-224. https://doi.org/10.3897/neobiota.67.59134
Listing of the 2750 introduced or invasive alien species with accepted names in France
Supplementary material 2 from: Renault D, Manfrini E, Leroy B, Diagne C, Ballesteros-Mejia L, Angulo E, Courchamp F (2021) Biological invasions in France: Alarming costs and even more alarming knowledge gaps. In: Zenni RD, McDermott S, García-Berthou E, Essl F (Eds) The economic costs of biological invasions around the world. NeoBiota 67: 191-224. https://doi.org/10.3897/neobiota.67.59134
Description of the different sectors of the InvaCost database
Supplementary material 5 from: Renault D, Manfrini E, Leroy B, Diagne C, Ballesteros-Mejia L, Angulo E, Courchamp F (2021) Biological invasions in France: Alarming costs and even more alarming knowledge gaps. In: Zenni RD, McDermott S, García-Berthou E, Essl F (Eds) The economic costs of biological invasions around the world. NeoBiota 67: 191-224. https://doi.org/10.3897/neobiota.67.59134
Number of cost estimates per year for France
Supplementary material 3 from: Renault D, Manfrini E, Leroy B, Diagne C, Ballesteros-Mejia L, Angulo E, Courchamp F (2021) Biological invasions in France: Alarming costs and even more alarming knowledge gaps. In: Zenni RD, McDermott S, García-Berthou E, Essl F (Eds) The economic costs of biological invasions around the world. NeoBiota 67: 191-224. https://doi.org/10.3897/neobiota.67.59134
Listing of the environment-taxonomic groupings
FIGURE 10 in Discovery of a new duiker species (Bovidae: Cephalophinae) from the Dahomey Gap, West Africa
FIGURE 10. Photograph of 4 skulls of Walters' Duiker for sale in a fetish market in Bohicon, Benin.
The contributions of lightning to biomass turnover, gap formation, and plant mortality in a tropical forest
<p>Lightning is a common source of disturbance, but its ecological effects in tropical forests are largely undescribed. Here we quantify the contributions of lightning strikes to forest turnover and plant mortality in a lowland Panamanian forest using a real-time lightning monitoring system. We examined 2195 lightning-damaged trees distributed among 93 different strikes. None exhibited scars or fires. On average, each strike disturbed 451 m2 (95% CI: 365-545 m2), created canopy gaps of 304 m2 (95% CI 198-454 m2), and caused 7.36 Mg of woody biomass turnover (CI: 5.36-9.65 Mg). Cumulatively, we estimate that lightning strikes in this forest create canopy gaps equaling 0.39% of forest canopy area, representing 20.1% of annual gap area formation, and are responsible for 16.1% of total woody biomass turnover. Trees, lianas, herbaceous climbers, and epiphytes were killed by lightning at rates 8-29 times greater than their baseline mortality rates in undamaged control sites. The likelihood of lightning-caused death was higher for trees, lianas, and herbaceous climbers than for epiphytes, and high liana mortality suggests that lightning is an important driver of liana turnover. These results indicate that lightning influences gap dynamics, plant community composition, and carbon storage capacity in some tropical forests.</p>
FIGURE 1 in A new species of Platyla (Mollusca: Gastropoda: Aciculidae) fills a biogeographic gap in the Mediterranean
FIGURE 1. Platyla jordai, sp. nov. Holotype (3.2 mm).
Figures 22-27 from: Scallion ML, Gibson GAP, Sharanowski BJ (2016) Revision of Paranastatus Masi (Eupelmidae, Eupelminae) with descriptions of four new species. ZooKeys 559: 59-79. https://doi.org/10.3897/zookeys.559.6134
Figures 22-27 - 22 Paranastatus pilosus holotype, lateral habitus 23 Paranastatus nigriscutellatus holotype, lateral habitus 24 Paranastatus parkeri holotype, lateral habitus 25 Paranastatus violaceus lectotype, lateral habitus 26 Paranastatus egregius lectotype, partial body in lateral view 27 Paranastatus egregius lectotype broken body parts glued to the point.
Figures 15-21 from: Scallion ML, Gibson GAP, Sharanowski BJ (2016) Revision of Paranastatus Masi (Eupelmidae, Eupelminae) with descriptions of four new species. ZooKeys 559: 59-79. https://doi.org/10.3897/zookeys.559.6134
Figures 15-21 - 15 Paranastatus verticalis holotype, lateral habitus 16 Paranastatus verticalis holotype, dorsal view 17 Paranastatus verticalis (Taveuni, Fiji), lateral habitus (JBWM Photo 2015-06) 18 Paranastatus verticalis (Taveuni, Fiji) in dorsal view (JBWM Photo 2015-06) 19 Paranastatus halko holotype, lateral habitus 20 Paranastatus bellus holotype, head in frontolateral view and antenna 21 Paranastatus bellus holotype, body in lateral view.
Figures 1-8 from: Scallion ML, Gibson GAP, Sharanowski BJ (2016) Revision of Paranastatus Masi (Eupelmidae, Eupelminae) with descriptions of four new species. ZooKeys 559: 59-79. https://doi.org/10.3897/zookeys.559.6134
Figures 1-8 - 1 Scanning electron micrograph (SEM) of Paranastatus halko, lower face in anterior view showing mandibular dentition (JBWM Photo 2015-01) 2 SEM of Paranastatus halko, gena in lateral view (JBWM Photo 2015-02) 3 Paranastatus nigriscutellatus, lower face in frontolateral view showing mandible dentition (JBWM Photo 2015-03). Inset: outline of mandible dentition showing four teeth 4 SEM of Paranastatus nigriscutellatus, head and anterior part of mesosoma in lateral view (JBWM Photo 2015-03) 5 Paranastatus verticalis, head in lateral view. Inset: outline of vertex-temple shape (JBWM Photo 2015-04) 6 Paranastatus verticalis holotype, lower face in anterior view showing fringe of setae below toruli 7 Paranastatus pilosus, head in lateral view. Inset: outline of vertex-temple shape (JBWM Photo 2015-05) 8 Paranastatus halko holotype, head in lateral view. Inset: outline of vertex-temple shape.
Figures 9-14 from: Scallion ML, Gibson GAP, Sharanowski BJ (2016) Revision of Paranastatus Masi (Eupelmidae, Eupelminae) with descriptions of four new species. ZooKeys 559: 59-79. https://doi.org/10.3897/zookeys.559.6134
Figures 9-14 - 9 Scanning electron micrograph (SEM) of Paranastatus pilosus, mesonotum in dorsal view (JBWM Photo 2015-05) 10 Paranastatus bellus holotype, head in dorsal view 11 SEM of Paranastatus pilosus, head and pronotum in dorsal view (JBWM Photo 2015-05) 12 Paranastatus nigriscutellatus holotype, mesonotum in dorsal view 13 Paranastatus violaceus lectotype, mesonotum in dorsal view 14 Paranastatus egregius lectotype, head in dorsal view.
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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.
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.