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30,334 results for “Responsiveness”
Figure 2 in An investigation of predator-induced defence responses in ciliated protozoa
Figure 2. Prey width distributions of Colpidium kleini from the experiment described in Table II, i.e. (a) in the absence of predators; (b) in the presence of Euplotes sp. Each distribution was calculated after 24 h and represents the mean of three replicates (n5150).
Figures 37–40 in Morphological alteration in response to endogeic habitat and ant association in two new planthopper species from New Caledonia (Hemiptera: Auchenorrhyncha: Fulgoromorpha: Delphacidae)
Figures 37–40. Notuchus ninguae sp. nov., male genitalia (holotype). (37) Anal segment, aedeagus, paramere in situ, left lateral aspect. (38–40) Aedeagus, right lateral, dorsal, and left lateral aspects, respectively. Scale bar: 0.1 mm.
Figures 21–23 in Morphological alteration in response to endogeic habitat and ant association in two new planthopper species from New Caledonia (Hemiptera: Auchenorrhyncha: Fulgoromorpha: Delphacidae)
Figures 21–23. Notuchus kaori sp. nov., male genitalia (holotype). (21) Anal segment, aedeagus, paramere in situ, left lateral aspect. (22, 23) Aedeagus, right lateral and dorsal aspects, respectively. Scale bar: 0.1 mm.
Figures 30–36 in Morphological alteration in response to endogeic habitat and ant association in two new planthopper species from New Caledonia (Hemiptera: Auchenorrhyncha: Fulgoromorpha: Delphacidae)
Figures 30–36. Notuchus ninguae sp. nov., male genitalia (holotype). (30, 31) Genital capsule, left lateral and ventrocaudal aspects, respectively. (32–34) Genital segment, left lateral, caudal, and ventral aspects, respectively. (35) Anal segment, dorsal aspect. (36) Parameres, ventrocaudal aspect. Scale bars: 0.1 mm.
Figures 24–29 in Morphological alteration in response to endogeic habitat and ant association in two new planthopper species from New Caledonia (Hemiptera: Auchenorrhyncha: Fulgoromorpha: Delphacidae)
Figures 24–29. Notuchus kaori sp. nov., nymph (5th instar). (24) Habitus, dorsal aspect. (25) Head and prothorax, dorsal aspect. (26) Head, anterior aspect. (27) Frons, anterior aspect. (28) Head and thorax, anterolateral aspect. (29) Distal margin of pedicel. Scale bars in mm.
Figures 14–20 in Morphological alteration in response to endogeic habitat and ant association in two new planthopper species from New Caledonia (Hemiptera: Auchenorrhyncha: Fulgoromorpha: Delphacidae)
Figures 14–20. Notuchus kaori sp. nov., male genitalia (holotype). (14, 15) Genital capsule, left lateral and ventrocaudal aspects, respectively. (16–18) Genital segment, left lateral, caudal, and ventral aspects, respectively. (19) Anal segment, dorsal aspect. (20) Parameres, ventrocaudal aspect. Scale bars: 0.1 mm.
Figures 4–13 in Morphological alteration in response to endogeic habitat and ant association in two new planthopper species from New Caledonia (Hemiptera: Auchenorrhyncha: Fulgoromorpha: Delphacidae)
Figures 4–13. Notuchus kaori sp. nov., adult male (paratype). (4) Habitus, dorsal aspect. (5) Detail: right tegmen, dorsal aspect. (6) Habitus, left lateral aspect. (7) Head, anterolateral aspect. (8) Left antenna. (9) Same, pedicel with sensory plaques and macrosetae. (10) Same as in Figure 9, detail. (11) Post-tibial spur. (12) Same as in Figure 11, detail. (13) Pretarsus (arolium and claws), ventral aspect. Scale bars in mm.
Figures 2, 3 in Morphological alteration in response to endogeic habitat and ant association in two new planthopper species from New Caledonia (Hemiptera: Auchenorrhyncha: Fulgoromorpha: Delphacidae)
Figures 2, 3. Notuchus kaori sp. nov., adult male. (2) Habitus with colour pattern, dorsal aspect, paratype male. (3) Colour pattern of abdomen, ventrolateral aspect (genital capsule removed), holotype male. Scale bar: 0.2 mm.
Figures 41, 42 in Morphological alteration in response to endogeic habitat and ant association in two new planthopper species from New Caledonia (Hemiptera: Auchenorrhyncha: Fulgoromorpha: Delphacidae)
Figures 41, 42. Paratrechina spec. (Formicidae), worker. (41) Habitus, lateral aspect. (42) Head, frontal aspect.
Figures 43, 44 in Morphological alteration in response to endogeic habitat and ant association in two new planthopper species from New Caledonia (Hemiptera: Auchenorrhyncha: Fulgoromorpha: Delphacidae)
Figures 43, 44. (43) Hypochthonella caeca China and Fennah (Hypochthonellidae), endogeic species (from Hoch 1994, used with permission). (44) Notuchus larvalis Fennah (Delphacidae), obligately cavernicolous (troglobitic) species (from Hoch 1994, used with permission). Scale bars: 0.5 mm.
Figure 14 in Avifaunal Responses to Warm Climate: The Message from Last Interglacial Faunas
Figure 14. Modern areas of co-occurrence for the Bir Tarfawi avifauna (18 analyzable taxa). The shaded area marks the co-occurrence area for the 16 Afrotropical taxa and the unshaded area the cooccurrence area of Chlamydotis undulata and Pterocles senegallus.
Figure 13 in Avifaunal Responses to Warm Climate: The Message from Last Interglacial Faunas
Figure 13. Modern areas of co-occurrence for the Welsh coastal cave avifaunas (Bacon Hole, Minchin Hole) (8 analyzable taxa). The shaded land area and coastal strips indicate the co-occurrence areas for landbirds and seabirds respectively.
Figure 10 in Avifaunal Responses to Warm Climate: The Message from Last Interglacial Faunas
Figure 10. Modern areas of co-occurrence for the Stuttgart-Untertürkheim avifauna (22 analyzable taxa).
Figure 9 in Avifaunal Responses to Warm Climate: The Message from Last Interglacial Faunas
Figure 9. Modern areas of co-occurrence for the Old Crow River avifauna (6 analyzable taxa). Note the smaller isolated area south of Hudson Bay, in the St Lawrence valley and the Maritime provinces.
Figure 2 in Avifaunal Responses to Warm Climate: The Message from Last Interglacial Faunas
Figure 2. Modern co-occurrence for LIG seabird and landbird faunas from the Los Angeles Basin (shaded areas). The unshaded area on the lower Colorado River marks an area where 19 out of 20 landbirds occur.
Multi-Angle, Multi-Distance Microphone Impulse Response Dataset
<p>This archive contains data generated as part of the PhD research of Juan Carlos Franco, investigating the timbral attributes related to the incident-angle-dependent response of microphones. </p> <p>The dataset of microphone impulse responses (IRs) comprises 25 microphones, including a Class-1 measurement microphone, covering the polar pattern variations of 7 of the microphones. The measurements were performed following a quasi-anechoic method, at incident angles from 0° to 355° with an angular resolution of 5°, and at source-to-microphone distances of 0.5 m, 1.25 m and 5m. </p> <p>Both normalised (-1 dBFS peak) and raw versions of the IRs have been rendered at bit-depths of 24-bit and 32-bit, with a sample rate of 48 kHz. </p> <p>A detailed description of the measurement procedure, as well as the equipment used, is provided in the associated journal paper [Franco et al. 2021].</p> <p><strong>References</strong></p> <p>J Franco, B Bǎcilǎ, T Brookes, E De Sena, "A multi-angle, multi-distance dataset of microphone impulse responses", J.Aud.Eng.Soc., Volume 70, Issue 10 pp. 882-893, October 2022, doi 10.17743/jaes.2022.0027</p>
Data from: Restoring marine ecosystems: spatial reef configuration triggers taxon-specific responses among early colonizers
<p>1. The longstanding debate in conservation biology on the importance of single large or several small (SLOSS) habitats for preserving biodiversity remains highly relevant, given the ongoing degradation and loss of natural habitats worldwide. Restoration efforts are often constrained by limited resources, and insights from SLOSS studies therefore have important implications if restoration efforts can be optimized by manipulating the spatial configuration of restored habitats. Yet, the relevance of SLOSS for habitat restoration remains largely unexplored.</p> <p>2. Here, we report the effects of spatial reef configuration on early colonization of marine organisms after restoring boulder reef habitats. Reefs were restored in single large (SL) and several small (SS) designs in the western Baltic Sea, where century-long boulder extraction has severely degraded large reef areas and likely exacerbated regional declines in commercially important gadoids (<i>Gadidae spp.</i>). We sampled the field sites using remote underwater video systems in a before-after control-impact (BACI) design and obtained probabilistic inferences on restoration and SLOSS effects from Bayesian hierarchical models.</p> <p>3. Probabilities of a positive restoration effect were high (>95%) for gadoids, labrids and demersal gobies, moderate (60-75%) for species richness and sand gobies, and low (<5%) for flatfish abundance. Notably, gadoid abundance increased 60-fold and 129-fold on average at SL and SS, respectively. The species composition at restored reefs deviated from control sites, mainly driven by large-bodied piscivores.</p> <p>4. Spatial reef configuration had the strongest effect on small-bodied mesopredators, including gobies, which were more abundant and driving a distinct species assemblage at SS. In addition to providing suitable conditions for reef species, results suggest that SS can also benefit soft-bottom taxa, possibly through a dispersed predator-mediated effect relative to SL. </p> <p><i>5. Synthesis and applications.</i> This study demonstrates that boulder reef restoration can strongly promote the abundance of exploited gadoids and is therefore a promising management tool to support top-down controls by predatory fishes in degraded marine systems. The higher abundance of mesopredators at SS reefs suggests that SLOSS could have long-term implications for trophic structure and resilience of restored habitats, and should therefore become an important facet within restoration strategies. </p>
Tunable photo-responsive elastic metamaterials
<p>Supplementary information for</p> <p>Gliozzi, A.S., Miniaci, M., Chiappone, A. <em>et al.</em> Tunable photo-responsive elastic metamaterials. <em>Nat Commun</em> <strong>11, </strong>2576 (2020). https://doi.org/10.1038/s41467-020-16272-y</p> <p>and raw data for Fig. 3 therein. Each file contains data for the spectra corresponding to each different temperature.</p> <p>The file has a suffix XXC, where XX indicates the temperature of the climate chamber in decrees C. Data are organized in two columns: the first is frequency in kHz, the second is FFT magnitude in dB</p> <p>The Video file 'represents the evolution of the transmission spectrum under illumination (data reltive to Fig. 2c in the main text), with 1 spectrum per second. At t=100s the sample is illuminated (first pillar) until t=360s. Then the spectrum reverts to the initial one</p>
Two-story frame with Bouc-Wen hysteretic links as a multi-degree of freedom nonlinear response simulator
<p><strong>Two-story frame with Bouc-Wen hysteretic links as a multi-degree of freedom nonlinear response simulator</strong></p> <p>Standardized datasets for tasks related to system identification applications, reduced-order or surrogate modelling applications. A multi-degree of freedom nonlinear response simulator benchmark proposed in the <em><strong>5th Edition of the Workshop on Nonlinear System Identification Benchmarks</strong></em> (April 2021, <a href="https://sites.google.com/view/nonlinear-benchmark/benchmarks">Link</a>).</p> <p>The open-access software implementation of the frame can be found in this <a href="https://github.com/KosVla/NonlinearBoucWenFrameBenchmark"><em><strong>Github repository</strong></em></a>.</p>
Fig. 3 in Diel movement patterns of Pacific sugar limpet, Patelloida saccharina (Gastropoda: Patellogastropoda: Lottiidae) in response to semi-diurnal tides of Samal Island, Philippines
Fig. 3. Movement patterns of Patelloida saccharina limpets in Catagman, Samal Island, during various lunar phases. A, New Moon, 27–28 March 2017; B, First Quarter, 4–5 April 2017; C, Full Moon, 9–10 April 2017; D, Last Quarter, 19–20 April 2017. The left and right y-axes correspond to the percentage of moving limpets and tidal height measurements in metres above chart datum (C.D.), respectively. Grey vertical bars represent the percentage of actively moving limpets during each lunar phase. The bar at the bottom corresponds to the day-night cycle: (from left to right) white = daytime, grey = transitioning to sunset, black = night-time, grey = sunrise. Note that the activity of P. saccharina limpets was observed during dark periods only, from sunset to night-time until before sunrise, as long as they were covered by the tide.
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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.