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26 results for “Incubation period”
Bergtold, 1917: Incubation Periods of Birds
Bergtold, William Harry. A Study of the Incubation Periods of Birds; What Determines Their Lengths,. Denver, Col.: Kendrick-Bellamy, 1917.<p></p>Bergtold, William Harry. A Study of the Incubation Periods of Birds; What Determines Their Lengths,. Denver, Col.: Kendrick-Bellamy, 1917.
Рис. 7. Интенсивность насиживания кΛаΔки в час (N = 84). ПериоΔы насиживания: 1 — 1–3 Δень; 2 — 4–6 Δень; 3 — 7–9 Δень; 4 — 10–12 Δень; 5 — 13–16 Δень Fig. 7. Intensity of clutch incubation per hour (N = 84). Incubation periods: 1 — 1–3 days; 2 — 4–6 days; 3 — 7–9 days; 4 — 10–12 days; 5 — 13–16 days in in the Ussuri region
Рис. 7. Интенсивность насиживания кΛаΔки в час (N = 84). ПериоΔы насиживания: 1 — 1–3 Δень; 2 — 4–6 Δень; 3 — 7–9 Δень; 4 — 10–12 Δень; 5 — 13–16 Δень Fig. 7. Intensity of clutch incubation per hour (N = 84). Incubation periods: 1 — 1–3 days; 2 — 4–6 days; 3 — 7–9 days; 4 — 10–12 days; 5 — 13–16 days
Haemosporidian parasites and incubation period influence plumage coloration in tanagers (Passeriformes: Thraupidae)
<p><span>Birds are visually oriented and use their plumage coloration as an important signaling trait in social communication. Males and females may have different patterns of plumage coloration, a phenomenon known as sexual dichromatism. Because males tend to have more complex plumages, sexual dichromatism is usually attributed to female choice. However, plumage coloration is partly condition-dependent, therefore other selective pressures affecting individuals' success may also drive the evolution of this trait. Here we used tanagers to study the relationships between dichromatism and plumage coloration complexity with parasitism by haemosporidians, investment in reproduction, and life-history traits. We screened blood samples from 2849 birds belonging to 52 tanager species for detecting haemosporidian parasites. We used publicly available data for plumage coloration, bird phylogeny, and life-history traits to run models with plumage dichromatism and complexity in males and females. We found that dichromatism was more pronounced in bird species with higher prevalence of haemosporidian parasites. Lastly, females with high plumage coloration complexity were associated with a longer incubation period. Our results indicate an association between haemosporidian parasites and plumage coloration suggesting that parasites impact mechanisms of both sexual selections, increasing differences between sexes, and social (non-sexual) selection, driving females to develop more complex colorations. </span></p>
Quantifying the Incubation Period of Tuberculosis: A Systematic Review
<p>Compiled dataset for the paper "Quantifying the Incubation Period of Tuberculosis: A Systematic Review"</p>
Haemosporidian parasites and incubation period influence plumage coloration in tanagers (Passeriformes: Thraupidae)
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Data from: Inter-colony variation in foraging flight characteristics of black-headed gulls Chroicocephalus ridibundus during the incubating period
Using GPS-loggers, we examined the influence of colony, sex, and bird identity on foraging flight characteristics of black-headed gulls <i>Chroicocephalus ridibundus </i>during the incubation period. We studied tracks of 36 individuals breeding in one urban and two rural colonies in Poland. Birds from both rural colonies performed the furthest flights (mean 8-12 km, up to 27 km) foraging mainly in agricultural areas. Gulls from the urban colony performed shorter flights (median 5 km, up to 17 km) visiting mainly urbanized areas and water bodies. We found that females performed longer flights and their flights parameters were less repeatable compared to males. Males from both rural colonies visited water bodies more frequently than females. In all colonies males (but not females) used habitats unproportionally to their availability in the vicinity. Relatively low inter-individual and relatively high intra-individual overlap in home ranges indicated considerable foraging site fidelity. Individuals specialized in the use of particular type of habitat performed shorter foraging flights compared to individuals using diverse habitats during their foraging flights. Our results indicate diverse foraging strategies of black-headed gulls, including generalists that explore various habitats and specialists characterized by high foraging site and habitat fidelity.
Figure 6. Temperature, April 2014 in Assessment of the incubation period for each sex of Turkish semiwild Northern Bald Ibis (Geronticus eremita)
Figure 6. Temperature, April 2014.
Figure 2. Temperature, March 2013 in Assessment of the incubation period for each sex of Turkish semiwild Northern Bald Ibis (Geronticus eremita)
Figure 2. Temperature, March 2013.
Figure 4. Temperature, March 2015 in Assessment of the incubation period for each sex of Turkish semiwild Northern Bald Ibis (Geronticus eremita)
Figure 4. Temperature, March 2015.
Data from: Ecological drivers and fitness consequences of incubation period in Ficedula albicollis (Collared Flycatcher): Insights from a long-term data set
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Incubation period length varies with temperature, female age, and clutch size in Protonotaria citrea (Prothonotary Warblers)
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Data from: Inter-colony variation in foraging flight characteristics of black-headed gulls Chroicocephalus ridibundus during the incubating period
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Soil net N mineralization over five incubation periods:Effect of Burning Patterns on Vegetation in the Fish Lake Burn Compartments
This study examines the effects of long-term prescribed burning treatments on vegetation structure and composition, productivity, and nutrient cycling in upland oak savanna and woodland vegetation. The basis for the study is an ongoing, experimental prescribed burning program begun in 1964 at Cedar Creek, and a similar program operating since 1962 on the adjacent Helen Allison Savanna property (owned by The Nature Conservancy). These prescribed burning programs are designed to subject upland oak communities (and some old fields) to different burn frequencies and patterns of burning, with the ultimate objectives of 1) restoring and maintaining the historically important savanna and open woodland vegetation, and 2) providing information about the effects of different burning patterns on vegetation structure and composition. This study addresses the latter of these two purposes and expands on it by also investigating possible influences of fire on resource availability (nutrients, water, and light) and net primary productivity. This study represents a continuation and expansion of experiments 015 and 094.
Data from: Association between severity of MERS-CoV infection and incubation period
We analyzed data for 170 patients in South Korea who had laboratory-confirmed infection with Middle East respiratory syndrome coronavirus. A longer incubation period was associated with a reduction in the risk for death (adjusted odds ratio/1-day increase in incubation period 0.83, 95% credibility interval 0.68–1.03).
Open-cup nesters in the Kalahari: incubation and egg-shading behaviour in passerines cannot be detected with temperature dataloggers during hot periods.
<p>The dataset includes the raw data and R scripts necessary to reproduce the analyses and figures explained in the manuscript "<span>Open-cup nesters in the Kalahari: incubation and egg-shading behaviour in passerines cannot be detected with temperature dataloggers during hot periods</span>"<strong>.</strong></p> <p>This dataset includes:</p> <p>- README.docx: Complete explanation of the different raw data used for the statistical analyses, together with the link to the R script where data is analyzed. We recommend to read this document before diving into the data and scripts.</p> <p>- Project data & code: Two separate folders for raw data and code.</p> <p> </p>
Data from: Association between the severity of influenza A(H7N9) virus infections and length of the incubation period
Background: In early 2013, a novel avian-origin influenza A(H7N9) virus emerged in China, and has caused sporadic human infections. The incubation period is the delay from infection until onset of symptoms, and varies from person to person. Few previous studies have examined whether the duration of the incubation period correlates with subsequent disease severity. Methods and Findings: We analyzed data of period of exposure on 395 human cases of laboratory-confirmed influenza A(H7N9) virus infection in China in a Bayesian framework using a Weibull distribution. We found a longer incubation period for the 173 fatal cases with a mean of 3.7 days (95% credibility interval, CrI: 3.4–4.1), compared to a mean of 3.3 days (95% CrI: 2.9–3.6) for the 222 non-fatal cases, and the difference in means was marginally significant at 0.47 days (95% CrI: -0.04, 0.99). There was a statistically significant correlation between a longer incubation period and an increased risk of death after adjustment for age, sex, geographical location and underlying medical conditions (adjusted odds ratio 1.70 per day increase in incubation period; 95% credibility interval 1.47–1.97). Conclusions: We found a significant association between a longer incubation period and a greater risk of death among human H7N9 cases. The underlying biological mechanisms leading to this association deserve further exploration.
Data from: Association between the severity of influenza A(H7N9) virus infections and length of the incubation period
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Data from: Association between severity of MERS-CoV infection and incubation period
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The Incidence and Incubation Period of False Positive Cultures in Shoulder Surgery
ClinicalTrials.gov study NCT02602548. IPD Sharing: YES. Countries: 0. Publications: 2.
Data from: Low genetic variance in the duration of the incubation period in a collared flycatcher (Ficedula albicollis) population
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