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PsPM-SMD: SCR, EMG, ECG, and respiration measurement in response to auditory startle probes
<p>This dataset includes skin conductance response (SCR), orbicularis oculi electromyogram (EMG), electrocardiogram (ECG) and bellows-based respiration measurements as well as sound channel recordings for each of 19 healthy unmedicated participants (6 males and 13 females aged 24.9 +/- 4.1 years, age stated in Khemka et al. 2017 was based on incomplete information) in response to 25 startle probes, as described in Khemka et al. (2017). ITI was determined randomly on each trial between 7-11 s. For 25% of the participants, SCR/ECG/respiration was not recorded. One data file contains only responses to 24 startle probes.</p>
Model of Sant Climent de Taüll: Impulse Responses and Auralisations.
<p>One of the most emblematic Romanesque paintings of La Vall de Boí, Catalonia, is the Pantocrator, a fresco found at Sant Climent de Taüll. However, only a small part of the church paintings is preserved whereas at the time of its construction, in 1123, its walls and columns were fully covered. If the church has experienced a complete transformation of its wall materials during the last 900 years, it can be assumed that its acoustic properties have also changed. This paper aims to recreate this acoustic transformation by building a computer model, analysing the acoustic effect of such paintings, and comparing three auralisation examples. The model is created using ODEON Geometric Acoustic Software, and calibrated using Impulse Responses taken in the real church. The results suggest that the paintings change the acoustics of the church, adding more than a second of reverb time, even with the relatively small dimensions of the church. This also affects speech intelligibility and music clarity.</p>
Figure 6. Response curve showing how each environmental variable affected the Maxent prediction. Variables A, B in PhylOgeOgraphy and pOtential distributiOn OF Sturnira lilium and S. giannae (ChirOptera: PhyllOstOmidae) With range eXtensiOn FOr S. giannae in the CerradO and Pantanal biOmes
Figure 6. Response curve showing how each environmental variable affected the Maxent prediction. Variables A, B, and C were the ones that most affected the potential distribution of S. giannae, and D, E, and F most affected the potential distribution of S. lilium. The curves show the average response of the 10 replicate Maxent runs (red) and the standard deviation (blue).
Figure 2 in Heart rate response and bimodal gas eXchange in three developmental stages of the bullfrog Lithobates catesbeianus (Anura: Ranidae)
Figure 2. Representative data recording of electrocardiogram (A) and aerial ventilation (B) in a premetamorphic Lithobates catesbeianus at 25°C. In B the signals show a ventilatory event where the tadpole renewed the air in its lungs, resulting in a marked drop in PO2 and an increase in PCO2. Following the ventilatory event, the expired air was mixed with the remaining air within the closed respirometry system, resulting in a PO2 slightly lower, and a PCO2 slightly greater, than before ventilation.
Figure 1 in Heart rate response and bimodal gas eXchange in three developmental stages of the bullfrog Lithobates catesbeianus (Anura: Ranidae)
Figure 1. Scheme of non-invasive apparatus to measure gas exchange in water (A) and air (B), and heart rate (C).
Figure 4 in Heart rate response and bimodal gas eXchange in three developmental stages of the bullfrog Lithobates catesbeianus (Anura: Ranidae)
Figure 4. Mass-specific oxygen consumption (A) and carbon dioxide released (B) for aerial (red lines and points) and aquatic (blue lines and points) gas exchange during development of Lithobates catesbeianus.
Figure 5 in Heart rate response and bimodal gas eXchange in three developmental stages of the bullfrog Lithobates catesbeianus (Anura: Ranidae)
Figure 5. Relationship between Log whole-body oxygen consumption (A) and carbon dioxide release (B) (µmol h-1) in 10 air (filled symbols) and water (open symbols), and Log10 body mass (g) in larval (blue triangles), premetamorphic (orange squares) and metamorphic (green circles) stages of Lithobates catesbeianus. Each point represents a measurement from a single animal. The regression lines correspond to aerial (red) and aquatic (blue) gas exchange. Dotted lines represent no significant correlation.
Figure 3. The effective population size through recent time for 3 in Comparative analyses of past population dynamics between two subterranean zokor species and the response to climate changes
Figure 3. The effective population size through recent time for 3 clades of Gansu zokor (Eospalax cansus).
Figure 1. A. Habitat where observations were carried out. B. Pupal clutches. C & D in A note on the defence by Eurema blanda Boisduval (Lepidoptera: Pieridae) pupae in response to oviposition behaviour of the chalcid wasp Brachymeria sp. (Hymenoptera: Chalcididae)
Figure 1. A. Habitat where observations were carried out. B. Pupal clutches. C & D. Left and right ways movement of pupa in response to Brachymeria sp. E. Female Brachymeria sp. F. Newly emerged Eurema blanda from collected pupae.
Figure. Constrained ordination plot as produced from canonical correspondence analysis (CCA). The variability of environmental variables is summarized on Axis 1 and Axis 2 of the constrained biplot, explaining the variability of the trophic groups included in the red fox's diet. Trophic groups are shown with black line (unfilled) pyramids, whereas environmental variables are shown with black filled pyramids. Proximity and distance of response centroids to predictor centroids indicate positive and negative correlations between them, respectively. in Factors affecting the diet of the red fox (Vulpes vulpes) in a heterogeneous Mediterranean landscape
Figure. Constrained ordination plot as produced from canonical correspondence analysis (CCA). The variability of environmental variables is summarized on Axis 1 and Axis 2 of the constrained biplot, explaining the variability of the trophic groups included in the red fox's diet. Trophic groups are shown with black line (unfilled) pyramids, whereas environmental variables are shown with black filled pyramids. Proximity and distance of response centroids to predictor centroids indicate positive and negative correlations between them, respectively.
Figure 1 in Biochemical response of two fish species of Gobiidae (Gobiiformes) to Cryptocotyle (Opisthorchiida, Heterophyidae) metacercariae infection from the mouth of the river Chernaya (Black Sea)
Figure 1. Cryptocotyle metacercariae: A – C. concavum; B – С. lingua; C – C. jejuna (scale 0.024 mm) (From: Machkevskiy & Belousova, 2012)
Dataset of "Synaptic Response of Fluidic Nanopores: The Connection of Potentiation with Hysteresis"
<p>This dataset supports the article published in <em>ChemPhysChem</em>.</p> <p>"Synaptic Response of Fluidic Nanopores: The Connection of Potentiation with Hysteresis"</p> <p> </p> <p>Raw data for the article "Synaptic Response of Fluidic Nanopores: The Connection of Potentiation with Hysteresis". For further details see the readme.txt file.</p>
Fig. 3 in Biological responses of Hypothenemus hampei (Coleoptera: Curculionidae) on Cenibroca artificial diet at different moisture content levels and relative humidities
Fig. 3. Coffee berry borer external feeding and reproduction behavior on Cenibroca artificial diet with 60% moisture content at 75% relative humidity. Notice how the external reproduction offers a simple separation of the coffee berry borer immature and adults from the diet for coffee berry borer parasitoid production. (A) Diet pellet 10 to 15 d afer infestation showing external feeding and development of first-generation offspring, arrows showing eggs of first generation. (B) Diet pellet 25 to 30 d afer infestation showing external feeding and development of first-generation offspring. Stages suitable for the African ectoparasitoids (Cephalonomia stephanoderis and Prorops nasuta) reproduction. (C) Diet pellet 35 to 40 d afer infestation showing external feeding and development of first-generation offspring. Notice the presence of mature and teneral females, arrows showing oviposition of second generation. (D) Diet pellet> 50 d afer infestation showing female production, suitable for the reproduction of the African ectoparasitoid P. nasuta.
Fig. 2 in Biological responses of Hypothenemus hampei (Coleoptera: Curculionidae) on Cenibroca artificial diet at different moisture content levels and relative humidities
Fig. 2. Loss of moisture content level percentage on a Cenibroca diet pellet with a 50, 60, and 70% moisture content level maintained at 65, 75, and 85% relative humidity. (95% confidence limits of the mean; n = 7 per evaluation time per treatment).
Fig. 1 in Biological responses of Hypothenemus hampei (Coleoptera: Curculionidae) on Cenibroca artificial diet at different moisture content levels and relative humidities
Fig. 1. Mean brood production of coffee berry borer per Cenibroca diet pellet with 50, 60, and 70% moisture content level maintained at 65, 75, and 85% relative humidity at different time periods. (95% confidence limits of the mean; n = 7 per evaluation time per treatment).
Fig. 6 in Laboratory feeding responses of Euthyrhynchus floridanus and Podisus maculiventris (Hemiptera: Pentatomidae) to the kudzu bug, Megacopta cribraria (Hemiptera: Plataspidae)
Fig. 6. Number of prey consumed by Podisus maculiventris (A) and Euthyrhynchus floridanus (B) when exposed to increasing density of Megacopta cribraria adults.
Fig. 5 in Laboratory feeding responses of Euthyrhynchus floridanus and Podisus maculiventris (Hemiptera: Pentatomidae) to the kudzu bug, Megacopta cribraria (Hemiptera: Plataspidae)
Fig. 5. Mean percent predation of Megacopta cribraria by Podisus maculiventris (I) without and (II) with alternative preya.
Fig. 4 in Laboratory feeding responses of Euthyrhynchus floridanus and Podisus maculiventris (Hemiptera: Pentatomidae) to the kudzu bug, Megacopta cribraria (Hemiptera: Plataspidae)
Fig. 4. Mean percent predation of Megacopta cribraria by Euthyrhynchus floridanus (I) without and (II) with alternative preya.
Fig. 6 in Predation functional response and life table parameters of Orius sauteri (Hemiptera: Anthocoridae) feeding on Megalurothrips usitatus (Thysanoptera: Thripidae)
Fig. 6. Age-stage predation rate (cxj) of Orius sauteri on the age-stage, 2-sex life table at 26 °C.
Fig. 3 in Predation functional response and life table parameters of Orius sauteri (Hemiptera: Anthocoridae) feeding on Megalurothrips usitatus (Thysanoptera: Thripidae)
Fig. 3. Relationship between density of Orius sauteri adults and intensity of scramble competition (I) on Megalurothrips usitatus adults.
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.