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151 results for “Nest site”

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dryad32/100

Data from: Going the distance: Influence of distance between boat noise and nest site on the behavior of paternal smallmouth bass

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publicAug 2020View details →
dryad32/100

Data from: Factors influencing nest site selection of the Laughing Dove (Spilopelia senegalensis) in an urban area in Karaj, Iran

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publicOct 2024View details →
dryad32/100

Data from: Antipredator behavioural syndromes and nest site choice in a freshwater turtle

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publicAug 2025View details →
dryad32/100

Data from: Nest site selection and nest survival of Black-backed Woodpeckers after wildfire

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publicAug 2019View details →
dryad32/100

Data from: No phenotypic plasticity in nest-site selection in response to extreme flooding events

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publicMar 2018View details →
dryad32/100

Data from: Breeding habitat and nest site selection by an obligatory “nest-cleptoparasite”, the Amur Falcon Falco amurensis

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publicNov 2019View details →
dryad32/100

Data from: The curious case of the camelthorn: competition, coexistence, and nest-site limitation in a multispecies mutualism

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publicJun 2015View details →
dryad32/100

Data from: Influence of mate and nest-site fidelity on a declining, urban avian population

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publicJun 2025View details →
dryad32/100

Data from: Physical and social cues shape nest-site preference and prey capture behavior in social spiders

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publicJan 2020View details →
dryad28/100

Pinyon jay (Gymnorhinus cyanocephalus) nest site selection in central New Mexico: Habitat Data to be used with AICc

<p>Pinyon Jays (<i>Gymnorhinus cyanocephalus</i>) are experiencing range wide population declines primarily in response to habitat degradation. Studies examining Pinyon Jay nest site selection in pinyon-juniper woodlands would be helpful in determining potential habitat management prescriptions. Therefore, we conducted a nest site selection study in Pinyon Jay breeding habitat in central New Mexico. We compared size and foliage characteristics of pinyon and juniper trees in 42 17.5-m radius plots around Pinyon Jay nests to 41 same-sized vegetation plots in random locations using binomial generalized linear models. The strongest model indicated that Pinyon Jays preferred nesting in areas with fewer dead juniper trees within pinyon-juniper habitats. Furthermore, Pinyon Jays built nests in pinyon and juniper trees with greater height (<i>p</i> &lt; 0.001) and nests were built below the average tree height in the plot (<i>p </i>= 0.001). Results suggest selective cutting of dead juniper and retention of tall, live pinyon or juniper trees may be used in pinyon-juniper woodlands to improve Pinyon Jay nesting habitat in the western United States.</p>

opencc-zeroSep 2020View details →
zenodo28/100

Mismatch between strong nest site selection and low survival of nests and broods for American woodcock and its implications for conservation

<p>Code and data for the paper entitled "Mismatch between strong nest site selection and low survival of nests and broods for Scolpax minor (American woodcock) and its implications for conservation" published in Ornitholgical Applications (2025). R code for landscape nest site selection is called <a href="../api/records/10927854/draft/files/landscape_nest_selectionornapplications.R/content" target="_blank" rel="noopener">landscape_nest_selectionornapplications.R</a> and data is called usedand5000availpoints.csv. R Code for local nest site selection is called&nbsp;<a href="../api/records/10927854/draft/files/local_nest_selectionornapplications.R/content" target="_blank" rel="noopener">local_nest_selectionornapplications.R</a> and data is called 2021_2022_nestdataveragedwithuse.csv. R code for nest survival is called&nbsp;<a href="../api/records/10927854/draft/files/nestsurvivalornapplications.R/content" target="_blank" rel="noopener">nestsurvivalornapplications.R</a> and data is called nestencounterwweather.csv and nestencounterhistoryweatherhabitat.csv. R code for brood survival is called <a href="../api/records/10927854/draft/files/broodsurvivalornapplications.R/content" target="_blank" rel="noopener">broodsurvivalornapplications.R</a> and data is called broodencounterhistoryweather.csv. All datasets are within the zipped folder called Nest Site Selection and Survival Analyses.zip</p>

opencc-by-4.0Apr 2024View details →
zenodo28/100

Figure 2 from: Michlewicz M, Tryjanowski P (2017) Anthropogenic waste products as preferred nest sites for Myrmica rubra (L.) (Hymenoptera, Formicidae). Journal of Hymenoptera Research 57: 103-114. https://doi.org/10.3897/jhr.57.12491

Figure 2 - Variation in median queen size (mesosoma length in mm) between control plots and plots with waste products in Myrmica rubra. Difference is statistically insignificant. Whiskers of the boxplot represents the range of minimum and maximum values.

opencc-by-4.0Jun 2017View details →
zenodo28/100

Figure 1 from: Michlewicz M, Tryjanowski P (2017) Anthropogenic waste products as preferred nest sites for Myrmica rubra (L.) (Hymenoptera, Formicidae). Journal of Hymenoptera Research 57: 103-114. https://doi.org/10.3897/jhr.57.12491

Figure 1 - Variation of measured nest parameters between control plots and plots with waste products in Myrmica rubra. A colony density (P &lt; 0.0001) B nest density (P &lt; 0.0001) C number of queens per colony (P = 0.06) D number of queens per nest (P = 0.26) E number of workers per colony (P=0.32) F number of workers per nest (P = 0.06). Numbers are given as median per plot (per 100 m2), whiskers of the boxplot represent the range of minimum and maximum values.

opencc-by-4.0Jun 2017View details →
zenodo28/100

FIGURE 2. Termite nests from site A in Termite nests in eolian backshore settings: An unusual record throughout the Quaternary in the Neotropical realm

FIGURE 2. Termite nests from site A. General view of the nests close to the shoreline (a), with sparse vegetation of grasses and ferns around the mounds, and detail of external nest morphology with no open chimneys (b) (nest A.6). The hypogean portion of nest A.10 with bottom passages vertically oriented is shown in (c). The schematic disposition of termite nests in site A allow observing that the closest nest is less than 30 m from shoreline (d), and nest's concentration in the flat areas of foredunes (e), almost 60 m far from shoreline.

opencc-by-4.0Dec 2021View details →
zenodo28/100

Figure 4 from: Boff S, Alves-dos-Santos I (2018) Cavities in bromeliad stolons used as nest sites by Euglossa cordata (Hymenoptera, Euglossini). Journal of Hymenoptera Research 62: 33-44. https://doi.org/10.3897/jhr.62.22834

Figure 4 Network-level analysis of larval provision of Euglossa cordata. Each orange rectangle represents the pollen type found in the brood cells. The green rectangles represent individual brood cell. The first number inside each green rectangle corresponds to the nest identity and the second number to the brood cell itself. The connection between rectangles (blue) shows the pollen types used as food for immature E. cordata. The width of each blue link corresponds to the frequency of pollen grains inside each brood cell. The content from brood cell N1.7, correspond to open cell in the nest 1 (see Fig. 2).

opencc-by-4.0Apr 2018View details →
zenodo28/100

Figure 1 from: Boff S, Alves-dos-Santos I (2018) Cavities in bromeliad stolons used as nest sites by Euglossa cordata (Hymenoptera, Euglossini). Journal of Hymenoptera Research 62: 33-44. https://doi.org/10.3897/jhr.62.22834

Figure 1 Location of study site. a The data was sampled on Ilha da Vitória, archipelago of Ilhabela, in São Paulo state b The habitat of the bromeliad on the rocks of the board, arrow highlights stolon of A. distichantha.

opencc-by-4.0Apr 2018View details →
zenodo28/100

Figure 2 from: Boff S, Alves-dos-Santos I (2018) Cavities in bromeliad stolons used as nest sites by Euglossa cordata (Hymenoptera, Euglossini). Journal of Hymenoptera Research 62: 33-44. https://doi.org/10.3897/jhr.62.22834

Figure 2 Details of two nests found inside stolons of bromeliads. In nest 1 only a part of the cell is shown. On the left side of nest 1 it is possible to see an open brood cell with fresh pollen in caramel color.

opencc-by-4.0Apr 2018View details →
zenodo28/100

Figure 3 from: Boff S, Alves-dos-Santos I (2018) Cavities in bromeliad stolons used as nest sites by Euglossa cordata (Hymenoptera, Euglossini). Journal of Hymenoptera Research 62: 33-44. https://doi.org/10.3897/jhr.62.22834

Figure 3 Stolon of A. distichantha with two connected nests of Euglossa cordata. Nest 2 and 3 were separated by resin and bee carcasses (arrow between nest 2 and nest 3; see details in Suppl. material 1: Fig. S1c). The entrance of nest 3 is indicated (arrow) and nest 3 is in detail after dissection (with scale, 2 cm).

opencc-by-4.0Apr 2018View details →
zenodo28/100

Figure. Map of the study area with the locations of actively used white-tailed eagle nests in the years 2009–2011. in Nest-site selection, breeding success, and diet of white-tailed eagles (Haliaeetus albicilla) in the Danube Delta, Romania

Figure. Map of the study area with the locations of actively used white-tailed eagle nests in the years 2009–2011.

opencc-by-4.0Feb 2015View details →
zenodo28/100

Figure 2 in Comparison of breeding biology aspects of Fluvicola nengeta (Aves: Tyrannidae) between two nesting sites

Figure 2. Plant species used as nesting substrate by F. nengeta.

opennotspecifiedJan 2018View details →

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Allen Brain Atlas

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DANDI Archive for NWB datasets

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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.

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OpenNeuro

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Last verified 2026-04-29Open record