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32 results for “resurgence”
Caldera resurgence during the 2018 eruption of Sierra Negra volcano, Galápagos Islands
<p>Key datasets associated with the 'Caldera resurgence during the 2018 eruption of Sierra Negra volcano, Galápagos Islands'. This are pre-eruption and co-eruption interferograms, IGUANA earthquake catalogue, list of earthquake times and magnitudes picked from station VCH1, and cGPS baseline timeseries.</p>
Fig. 1 in Incorporation of biorational insecticides with neonicotinoids to combat resurgence of Tetranychus urticae (Prostigmata: Tetranychidae) on rose
Fig. 1. Preference and non-preference test for spider mites by pro- viding imidacloprid (IMD)-or acetamiprid (ACT)-treated and untreated rose leaves as 2 choices at different days afer treatment (DAT) and observing the percentage of spider mites reaching a specific choice. Asterisk indicates significant difference between treatment and untreated control (P = 0.05, χ2 goodness of fit).
Fig. 2 in Recent documentation of the tropical bed bug (Hemiptera: Cimicidae) in Florida since the common bed bug resurgence
Fig. 2. Auto-Montage photograph of a dissected pronotum from Cimex lectularius (A) and Cimex hemipterus (B).
Fig. 1 in Recent documentation of the tropical bed bug (Hemiptera: Cimicidae) in Florida since the common bed bug resurgence
Fig. 1. Auto-Montage photograph of an adult Cimex hemipterus male collected from Brevard County on the right and an adult Cimex lectularius male on the lef. Arrows are pointing to the lateral pronotum margin on both species.
Analogue models of caldera resurgence: database of models and elaborations
<p>This dataset presents the results of an experimental series of analogue models performed to investigate caldera resurgence processes, particularly the setting of the Los Potreros caldera that belongs to the Los Humeros Volcanic Complex (Puebla State, Mexico). Our experimental series was designed adopting a parametric approach, which consisted in the systematic variation of controlling parameters, such as: depth of intrusion, overburden thickness above the analogue magma chamber, presence of inherited discontinuities. Structures of models have been analysed quantitatively by means of (i) photogrammetric Digital Elevation Model reconstruction, (ii) semi-automatic fault pattern quantification and (iii) Digital Particle Image Velocimetry techniques. In this dataset, we show the row data and specific elaborations supporting the interpretation of modelling results.</p>
Data from: Predator foraging response to a resurgent dangerous prey
Prey switching occurs when a generalist predator kills disproportionately more of an abundant prey species and correspondingly spares a rarer species. Although this behaviour is a classic stabilizing mechanism in food web models, little is known about its operation in free-living systems which often include dangerous prey species that resist predation. We used long-term (1995–2015) data from a large mammal system in northern Yellowstone National Park, USA, to understand how prey preference of a wild, generalist predator (Canis lupus) responds to a shift in prey species evenness involving rising numbers of dangerous prey (Bison bison) and dropping numbers of relatively safer prey (Cervus elaphus). Contrary to the prey switching hypothesis, wolves attacked and killed disproportionately more of the rarer, but safer, species. Wolves maintained a strong preference against bison even when this species was more than twice as abundant as elk. There was also evidence that wolves were increasingly averse to hunting bison as relative bison abundance increased. Wolves seldom hunted bison because capture success was limited to a narrow set of conditions: larger packs (>11 wolves) chasing smaller herds (10–20 bison) with calves. Wolves scavenged bison carrion instead and did so more frequently as bison abundance increased. Our study demonstrates the overarching importance of prey vulnerability to understanding the prey preferences of generalist predators in ecological communities with dangerous prey. The formidable defences of such prey diminish the potential for switching and its stabilizing influence on population dynamics. In these communities, shifts from hunting to scavenging are perhaps more likely than shifts in prey preference. The assumption of switching may therefore overestimate the stability of multi-prey systems that include dangerous prey species.
Project Resurgence Communication Trial
ClinicalTrials.gov study NCT04418947. IPD Sharing: NO. Countries: 1. Publications: 1.
Resurgence as Choice: Basic and Clinical Studies
ClinicalTrials.gov study NCT03423940. IPD Sharing: YES. Countries: 1. Publications: 12.
Marine mammal recovery is associated with the resurgence of a nematode parasite
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Data from: Early warning signals of malaria resurgence in Kericho, Kenya
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Data from: Predator foraging response to a resurgent dangerous prey
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Effects of transient, persistent, and resurgent sodium currents on excitability and spike regularity in vestibular ganglion neurons
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Data from: Decreased bioefficacy of long-lasting insecticidal nets and the resurgence of malaria in Papua New Guinea
<p>Papua New Guinea (PNG) has the highest malaria transmission outside of Africa. Long-lasting insecticidal nets (LLINs) are believed to have helped to reduce average malaria prevalence in PNG from 15.7% in 2008 to 1% in 2014. Since 2015 malaria indicators in PNG have risen significantly. In the present study, we observed a drastically decreased bioefficacy of unused LLINs with manufacturing dates between 2013 and 2019 collected from villages and LLIN distributors in PNG. Specifically, of the tested n=167 LLINs manufactured between 2013 and 2019 only 16% achieved <a>≥ 80% 24h-mortality or ≥ 95% 60 min-knockdown in cone bioassays </a>conducted with pyrethroid susceptible <i>Anopheles farauti</i> mosquitoes. In contrast, all (100%, n=25) LLINs with manufacturing dates between 2007 and 2012 achieved ≥ 80% 24h-mortality or ≥ 95% 60 min-knockdown. This difference was extremely statistically significant. We hypothesise that decreased bioefficacy of LLINs has contributed to the malaria resurgence in PNG.</p>
Data and code for the manuscript titled "Persistence of SARS-CoV-2 immunity, Omicron's footprints, and projections of epidemic resurgences in South African population cohorts"
<p>Data and code for the manuscript titled “Persistence of SARS-CoV-2 immunity, Omicron’s footprints, and projections of epidemic resurgences in South African population cohorts”</p>
FIGURE 35 in Resurgence of a forgotten Southern Brazil endemic species: taxonomic position, redescription, and spatio-temporal distribution of Porosagrotis carolia Schaus, 1929 (Lepidoptera: Noctuidae: Noctuinae)
FIGURE 35. Number of known specimens of Feltia carolia (Schaus, 1929) comb. nov. (n=53) by month of collection, from 1922 to 2014; light gray: records from the literature and specimens in entomological collections; dark gray: specimens collected in light traps from 1998 to 1999 (see text for details).
FIGURES 13–17 in Resurgence of a forgotten Southern Brazil endemic species: taxonomic position, redescription, and spatio-temporal distribution of Porosagrotis carolia Schaus, 1929 (Lepidoptera: Noctuidae: Noctuinae)
FIGURES 13–17. Feltia carolia (Schaus, 1929) comb. nov., labial palpus, thorax and appendages. 13. Labial palpus, lateral. 14. Thorax, dorsal. 15. Forewing, upper side. 16. Male wing coupling. 17. Female wing coupling. Arrows point out frenula, retinacula and patches of enlarged scales. Scale bars: Fig. 13 = 0.5 mm, Fig. 14= 2 mm, Fig. 15= 5 mm, Figs. 16–17 = 0.5 mm.
FIGURES 7–12 in Resurgence of a forgotten Southern Brazil endemic species: taxonomic position, redescription, and spatio-temporal distribution of Porosagrotis carolia Schaus, 1929 (Lepidoptera: Noctuidae: Noctuinae)
FIGURES 7–12. Feltia carolia (Schaus, 1929) comb. nov., head and appendages. 7. Head, anterior. 8. Frons tubercle, anterior. 9. Head, lateral. 10. Male antenna in its widest part, ventral. 11. Male antenna distal segments, lateral. 12. Female antenna, lateral. Scale bars: Fig. 7 = 1 mm, Fig. 8 = 0.2 mm, Figs 9–11 = 0.5 mm, Fig. 12 = 0.2 mm.
FIGURES 26–27 in Resurgence of a forgotten Southern Brazil endemic species: taxonomic position, redescription, and spatio-temporal distribution of Porosagrotis carolia Schaus, 1929 (Lepidoptera: Noctuidae: Noctuinae)
FIGURES 26–27. Feltia carolia (Schaus, 1929) comb. nov., male genitalia, lateral. 26. genitalia with right valva removed. 27. Valva. Scale bars: Fig. 26 = 1 mm, Fig. 27 = 0.5 mm.
FIGURES 1–6 in Resurgence of a forgotten Southern Brazil endemic species: taxonomic position, redescription, and spatio-temporal distribution of Porosagrotis carolia Schaus, 1929 (Lepidoptera: Noctuidae: Noctuinae)
FIGURES 1–6. Feltia carolia (Schaus, 1929) comb. nov., dorsal and ventral habitus.1–2. Male, Lagoa Vermelha, Rio Grande do Sul, Brazil (MCTP 9536). 3–4 Male, Lagoa Vermelha, Rio Grande do Sul, Brazil (MCTP 9538). 5–6. Female, Cambará do Sul, Rio Grande do Sul, Brazil (CLAM 00021). Scale bar = 1 cm.
FIGURE 34 in Resurgence of a forgotten Southern Brazil endemic species: taxonomic position, redescription, and spatio-temporal distribution of Porosagrotis carolia Schaus, 1929 (Lepidoptera: Noctuidae: Noctuinae)
FIGURE 34. Feltia carolia (Schaus, 1929) comb. nov., spatial distribution. Black dots indicate localities of standardized samplings; yellow stars, the presence of F. carolia comb. nov., and the question mark, the state of the type locality; green shaded areas indicates roughly areas of southern Brazilian Campos, according to Overbeck et al. (2007).
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.