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zenodo40/100

FIGURE 1. AMNH FARB 6517 in A Second Specimen of Citipati osmolskae Associated with a Nest of Eggs from Ukhaa Tolgod, Omnogov Aimag, Mongolia

FIGURE 1. AMNH FARB 6517 the type specimen of Oviraptor philoceratops found associated with a nest of eggs. From Osborn (1924).

opencc-by-4.0Apr 2018View details →
zenodo40/100

FIGURE 2. IGM 100 in A Second Specimen of Citipati osmolskae Associated with a Nest of Eggs from Ukhaa Tolgod, Omnogov Aimag, Mongolia

FIGURE 2. IGM 100/979. The nesting Citipati osmolskae as it was first found at Ukhaa Tolgod in 1993. Left Amy Davidson, right Louis Chiappe.

opencc-by-4.0Apr 2018View details →
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Imidacloprid exposure through soil and its effect on Anthophora plumipes, a ground-nesting bee

<p>These are the raw data files is associated with the manuscript titled "Neonicotinoid exposure through soil and its effect on Anthophora plumipes, a ground-nesting bee".</p>

opencc-by-4.0Mar 2024View details →
dryad40/100

Concrete habitat: Impervious surface in nest vicinity is associated with avian fitness decline in two urban adapters

<p>The conversion of natural habitats to impervious surfaces in cities affects biotic and abiotic attributes of urban ecosystems. Detailed information on the gradual influence of impervious surfaces on reproductive success, however, is lacking. Using five years of nestbox-breeding great tit and blue tit breeding data collected across various habitat types within and outside a Central-Eastern European capital city, we quantified the impact of impervious surfaces on avian reproductive success. Impervious surfaces strongly and negatively covaried with the number of fledged young in both species: a 50% increase in impervious surface resulted in 2.93 (95% CI: -4.27; -1.58) fewer blue tit offspring fledging the nest, and 3.51 (95% CI: -4.79; -2.23) fewer great tit offspring fledging the nest, thus halving the reproductive output of two widespread urban species. These results provide benchmark values of avian productivity for ecologists and urban policy makers, and for the management of urban areas.</p>

opencc-zeroMar 2024View details →
zenodo40/100

FIGURE 6 in A trunk-nesting form of the processionary caterpillar Ochrogaster lunifer (Lepidoptera: Notodontidae) restricted to a single host species Corymbia tessellaris (Myrtaceae), with some comparisons to the ground-nesting form

FIGURE 6 The temperature inside nests of O. lunifer larvae compared with ambient over a 24 h cycle: (a) tree-hugger nests (n = 9) and (b) ground nests (n = 14). The data point for each nest is the mean of seven to eight consecutive days of measurement.

opencc-by-4.0Apr 2023View details →
zenodo40/100

FIGURE 5 in A trunk-nesting form of the processionary caterpillar Ochrogaster lunifer (Lepidoptera: Notodontidae) restricted to a single host species Corymbia tessellaris (Myrtaceae), with some comparisons to the ground-nesting form

FIGURE 5 Ochrogaster lunifer (a) pupa with cocoon cut open and (b) newly emerged adult female of the tree-hugger form.

opencc-by-4.0Apr 2023View details →
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FIGURE 1 in A trunk-nesting form of the processionary caterpillar Ochrogaster lunifer (Lepidoptera: Notodontidae) restricted to a single host species Corymbia tessellaris (Myrtaceae), with some comparisons to the ground-nesting form

FIGURE 1 The egg masses and nests of the two forms of O. lunifer co-occurring at Gatton, QLD: (a) tree-hugger egg mass in the fork of a twig, (b) tree-hugger nest on the trunk of C. tessellaris, (c) three ground egg masses at base of an Acacia sp., and (d) a ground nest.

opencc-by-4.0Apr 2023View details →
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FIGURE 2 in A trunk-nesting form of the processionary caterpillar Ochrogaster lunifer (Lepidoptera: Notodontidae) restricted to a single host species Corymbia tessellaris (Myrtaceae), with some comparisons to the ground-nesting form

FIGURE 2 The confirmed locations of the O. lunifer tree-hugger form and the range of C. tessellaris occurrence in Australia. C. tessellaris data from the Atlas of Living Australia.

opencc-by-4.0Apr 2023View details →
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FIGURE 3 in A trunk-nesting form of the processionary caterpillar Ochrogaster lunifer (Lepidoptera: Notodontidae) restricted to a single host species Corymbia tessellaris (Myrtaceae), with some comparisons to the ground-nesting form

FIGURE 3 The orientation of egg masses and nests of O. lunifer: (a) tree-hugger egg masses, (b) ground-nester egg masses, (c) tree-hugger nests, and (d) ground nests. Dashed line is the mean orientation.

opencc-by-4.0Apr 2023View details →
zenodo40/100

Fig. 33 in Nesting Biologies and Immature Stages of the Tapinotaspidine Bee Genera Monoeca and Lanthanomelissa and of Their Osirine Cleptoparasites Protosiris and Parepeolus (Hymenoptera: Apidae: Apinae)

Fig. 33. Cocoon of Lanthanomelissa betinae from which larva had been removed, lateral view. Fig. 34. Cocoon of Parepeolus minutus from which larva had bee removed, lateral view. Fig. 35. Inner surface of front end of cocoon of Lanthanomelissa betinae showing complete covering by pale feces. Fig. 36. Inner surface of front end of cocoon of Parepeolus minutus showing central area that is not coated by feces.

opencc-by-4.0Jan 2006View details →
zenodo40/100

Fig. 1 in Nesting Biologies and Immature Stages of the Tapinotaspidine Bee Genera Monoeca and Lanthanomelissa and of Their Osirine Cleptoparasites Protosiris and Parepeolus (Hymenoptera: Apidae: Apinae)

Fig. 1. Nesting site of Monoeca haemorrhoidalis, showing dense ground cover in foreground. Fig. 2. Close­up of two nest entrances of same. Fig. 3. Main burrow of Monoeca haemorrhoidalis showing repetitive tamping impressions on shiny burrow wall. Fig. 4. Monoeca haemorrhoidalis, spiral inner surface of cell closure. Figs. 5, 6. Closure ends of cells of Monoeca haemorrhoidalis, showing plugged entrance holes made by females of Protosiris gigas; holes are filled by them as they depart.

opencc-by-4.0Jan 2006View details →
zenodo40/100

Fig. 1 in The Influence Of Nest Size On Heat Loss Of Penduline Tit Eggs

Fig. 1. Changes in internal egg temperatures (mean °C) during trials with Penduline Tit nests (treatments: ambient temperature – clutch size)

opencc-by-4.0Mar 2005View details →
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Fig. 2 in The Influence Of Nest Size On Heat Loss Of Penduline Tit Eggs

Fig. 2. Effects of nest thickness on terminal temperatures in relation to ambient temperature and clutch size. Each symbol represents one nest (N= 20 nests, all nests were measured in all treatments). We used least-squares regression to estimate the best fit to each pair of treatments separately (regression equations, 25°C &amp; 9 eggs: terminal temperature = 27.64 + 0.05 × nest thickness; 25°C &amp; 3 eggs: terminal temperature = 27.56 + 0.01 × nest thickness; 10°C &amp; 9 eggs: terminal temperature = 16.29 + 0.19 × nest thickness; 10°C &amp; 3 eggs: terminal temperature = 15.66 + 0.08 × nest thickness)

opencc-by-4.0Mar 2005View details →
zenodo40/100

Fig. 1. Residentmalependulinetitsreacttoplaybacksongandadummypendulinetit aroundtheirnest. Behaviouralresponsesincludedattacking, i.e in Acoustic Signalling In Eurasian Penduline Tits Remiz Pendulinus: Repertoire Size Signals Male Nest Defence

Fig. 1. Residentmalependulinetitsreacttoplaybacksongandadummypendulinetit aroundtheirnest. Behaviouralresponsesincludedattacking, i.e. peckingatthedummy, as

opencc-by-4.0Mar 2013View details →
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Fig. 2 in Acoustic Signalling In Eurasian Penduline Tits Remiz Pendulinus: Repertoire Size Signals Male Nest Defence

Fig. 2. SonogramsofsometypicalsyllabletypesofEurasianpendulinetits. Songbouts mayconsistofvarioussyllables (topandbottomsonograms) ormayincludemonotone

opencc-by-4.0Mar 2013View details →
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Fig. 3 in Acoustic Signalling In Eurasian Penduline Tits Remiz Pendulinus: Repertoire Size Signals Male Nest Defence

Fig. 3. Approachdistance (a) and % behaviouralresponses (b) towardsanintruderinre- lationtotheresidentmale'sownrepertoiresize. Behaviouralresponsesincludedcalling, singing, tailquiveringandattacking. Opencirclesindicateresponsesofchallengedresi- dentsonsmallrepertoireplayback, whereasfilledcirclesindicatethesamemales' respons- esonlargerepertoireplayback. Notethatpointsshownontheupperhalfregionof (a) represent males that were mostly present very close to their nest (15 m from the stimulus,

opencc-by-4.0Mar 2013View details →
zenodo40/100

Fig. 2 in Do Different Plasticine Eggs In Artificial Ground Nests Influence Nest Survival?

Fig. 2. Daily survival rates (+1SE) of different egg types in small mammal traps. Q: small mammal trap baited with one quail egg; NP: natural plasticine egg; WP: white coloured plasticine egg

opencc-by-4.0Nov 2012View details →
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Fig. 1 in Do Different Plasticine Eggs In Artificial Ground Nests Influence Nest Survival?

Fig. 1. Daily survival rates (+1SE) of artificial ground nests with different egg combinations (Q+Q – nest baited with two quail eggs, Q+NP – one quail and one natural plasticine eggs, Q+WP – one quail and one white coloured plasticine eggs). White bars represent the survival rates, when damage or disappearance of any types of egg in the nest was considered as a predation event; gray bars represent the survival rates, when only damage or disappearance of quail eggs was considered as a predation event. Stars indicate significant differences, **: P &lt;0.05; ***: P &lt;0.01

opencc-by-4.0Nov 2012View details →
zenodo40/100

Stronger negative species interactions in the tropics supported by a global analysis of nest predation in songbirds

<p>Original data, phylogeny and list of studies from: &quot;Stronger negative species interactions in the tropics supported by a global analysis of nest predation in songbirds&quot;</p>

opencc-by-4.0Dec 2021View details →
zenodo40/100

Figures 7–8. Aporus hirsutus prey transport. 7 in Nesting behavior, ecology, and functional morphology of the trapdoor spider-hunting spider wasp Aporus (Plectraporus) hirsutus (Banks) (Hymenoptera: Pompilidae)

Figures 7–8. Aporus hirsutus prey transport. 7) Aporus hirsutus female dragging Aptostichus simus juvenile backwards across sand, grasping end of its right foreleg with her mandibles. Sandy coastal back dunes, Santa Barbara County, CA; 17 June 2015; A. Abela. Photograph © Alice Abela. 8) Aporus hirsutus female dragging Aptostichus simus juvenile backwards across sand, grasping tibia of its 2nd left leg with her mandibles. The wasp's wings are folded on her dorsum, sandy coastal back dunes, Santa Barbara County, CA; 17 June 2015; A. Abela. Photograph © Alice Abela.

opencc-by-4.0Dec 2021View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

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behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record