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806 results for “cavities”
Laser ablation - rectangular cavity
<p>Laser ablation simulation using CutFEM - rectangular cavity</p>
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).
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.
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.
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).
Figures 4-6 from: García-Ulloa D, Landa-Jaime V, Góngora-Gómez AM, García-Ulloa M, Hernández-Sepúlveda J (2019) Sexual and reproductive traits of the pearl oyster shrimp Pontonia margarita (Decapoda: Palemonidae), symbiotically inhabiting the mantle cavity of the rugose pen shell Pinna rugosa (Bivalvia: Pinnidae). Zoologia 36: 1-7. https://doi.org/10.3897/zoologia.36.e29774
Figures 4-6 Pontoniamargarita: (4) male (small and whitish) and female (large and orange); (5) female (circled) in the mantle cavity of P.rugosa; (6) ovigerous female. Scale bar = 1 cm.
Figure 7 from: García-Ulloa D, Landa-Jaime V, Góngora-Gómez AM, García-Ulloa M, Hernández-Sepúlveda J (2019) Sexual and reproductive traits of the pearl oyster shrimp Pontonia margarita (Decapoda: Palemonidae), symbiotically inhabiting the mantle cavity of the rugose pen shell Pinna rugosa (Bivalvia: Pinnidae). Zoologia 36: 1-7. https://doi.org/10.3897/zoologia.36.e29774
Figure 7 Relationship between Pontoniamargarita total body length (mm) and Pinnarugosa shell height (mm). Regressions for females and males were r = 0.32 (p = 0.08) and r = 0.18 (p = 0.46), respectively.
Figures 1-3 from: García-Ulloa D, Landa-Jaime V, Góngora-Gómez AM, García-Ulloa M, Hernández-Sepúlveda J (2019) Sexual and reproductive traits of the pearl oyster shrimp Pontonia margarita (Decapoda: Palemonidae), symbiotically inhabiting the mantle cavity of the rugose pen shell Pinna rugosa (Bivalvia: Pinnidae). Zoologia 36: 1-7. https://doi.org/10.3897/zoologia.36.e29774
Figures 1-3 Morphometric measurements of Pinnarugosa. (1) Shell height; (2) shell length; (3) shell width.
Plate III. Tyrannosaurus rex. Section of skull showing brain cavity. Amer. Mus. No. 5029: Scale 1/2. in Crania of Tyrannosaurus and Allosaurus
Plate III. Tyrannosaurus rex. Section of skull showing brain cavity. Amer. Mus. No. 5029: Scale 1/2.
Text-fig. 2. Gemmacrinus perplexus PROKOP et PETR, 1989. A – Specimen NM-L31684; cavity of the conch of gastropod Epiptychia? PERNER, 1911 with preserved calyxes of crinoid Gemmacrius perplexus PROKOP et PETR, 1989. Scale bar represents 5 mm. B – The same specimen; best preserved calyx in detail. Lower Devonian, Pragian, Koněprusy Limestone, Suchomasty, "Na Plešivci" quarry. Scale bar represents 1 mm. in Unique Discovery Of The Crinoid Gemmacrinus Perplexus Prokop Et Petr, 1989 In The Lower Devonian, Koněprusy Limestone (Barrandian Area, The Czech Republic)
Text-fig. 2. Gemmacrinus perplexus PROKOP et PETR, 1989. A – Specimen NM-L31684; cavity of the conch of gastropod Epiptychia? PERNER, 1911 with preserved calyxes of crinoid Gemmacrius perplexus PROKOP et PETR, 1989. Scale bar represents 5 mm. B – The same specimen; best preserved calyx in detail. Lower Devonian, Pragian, Koněprusy Limestone, Suchomasty, "Na Plešivci" quarry. Scale bar represents 1 mm.
TMD cavity
<p>Data files used to generate the main figures in the manuscript.</p>
Figure data for article "Fluctuation-induced Bistability of Fermionic Atoms Coupled to a Dissipative Cavity"
<p>The files contain the data depicted in the figures of the article "Fluctuation-induced Bistability of Fermionic Atoms Coupled to a Dissipative Cavity", arXiv:2409.16035 (2024)</p> <p>The format of the data and to which figure it corresponds is described in the file "read_me_metadata.txt".</p>
Simulated of PRACE Using a Transparent Uterine Cavity Model
Open the record for dataset details and reuse information.
Simulation Results on Size-Dependent Surface Charging of Lunar Cavities Exposed to the Solar Wind
<p>Here we present the numerical simulation data from Nakazono and Miyake (2025), titled "Size-Dependent Surface Charging of Lunar Cavities Exposed to the Solar Wind."</p>
Increased microclimatic variation in artificial nests does not create ecological traps for a secondary cavity breeder, the European roller
Artificial devices are increasingly used in conservation measures to mitigate the disappearance of natural habitats. However, few studies have demonstrated their benefits for the target species, and they may pose a risk of creating ecological traps. This occurs when lower individual fitness is found in artificial habitats that are more attractive than their natural equivalents. In this study, we tested the ecological trap hypothesis on a dense population of European rollers Coracias garrulus breeding in both natural cavities and nest-boxes. Our initial prediction was that the more stressful microclimatic conditions of nest-boxes would lead to reduced fitness of European rollers, thus creating an ecological trap. The results showed that nest-boxes were preferred over natural cavities. Despite significantly more extreme microclimatic conditions in nest-boxes, we found similar breeding parameters between artificial and natural nest types. Our results also suggest that European rollers selected the nest-boxes which best buffered the temperature, thus avoiding potential ecological traps. Overall our results led to the conclusion that nest-boxes do not create ecological traps for European rollers in this study area. However, other species may be more sensitive to microclimatic variations or less able to avoid the least favourable nest-boxes. These findings could help to inform the placement of nest-boxes in order to reduce extreme temperatures and variation in humidity rates. Future studies could compare nest types for other fitness parameters, such as juvenile body condition or survival. We also recommend the ecological trap hypothesis as a useful framework to evaluate the outcomes of artificial devices used for conservation.
Figure 2 from: de Ázara LN, Bernardi LFO, Ferreira RL (2016) The first survey on harvestmen in Brazilian artificial cavities, with notes on distribution and natural history. Subterranean Biology 17: 31-53. https://doi.org/10.3897/subtbiol.17.6762
Figure 2 - Artificial cavities in: A, B, C Alagoa D and E Padre Paraíso F Caraí G Mariana H São José da Safira I Caeté J Mariana.
Figure 1 from: de Ázara LN, Bernardi LFO, Ferreira RL (2016) The first survey on harvestmen in Brazilian artificial cavities, with notes on distribution and natural history. Subterranean Biology 17: 31-53. https://doi.org/10.3897/subtbiol.17.6762
Figure 1 - Map of the state of Minas Gerais, Brazil, showing the biomes and municipalities in which the artificial cavities are situated: a Alagoa b Ataléia c Caeté d Caraí e Mariana f Mateus Leme g Medina h Nova Lima i Novo Oriente de Minas j Ouro Preto k Padre Paraíso l São José da Safira m Vazante.
Figure 5 from: de Ázara LN, Bernardi LFO, Ferreira RL (2016) The first survey on harvestmen in Brazilian artificial cavities, with notes on distribution and natural history. Subterranean Biology 17: 31-53. https://doi.org/10.3897/subtbiol.17.6762
Figure 5 - Mitogoniella mucuri inside the Túnel do Garrafão (Alagoa) A Female guarding eggs on the wall of the mine B Female guarding immatures on the wall of the mine.
Figure 4 from: de Ázara LN, Bernardi LFO, Ferreira RL (2016) The first survey on harvestmen in Brazilian artificial cavities, with notes on distribution and natural history. Subterranean Biology 17: 31-53. https://doi.org/10.3897/subtbiol.17.6762
Figure 4 - Individuals inside the artificial cavities A Longiperna trembao (Caeté: Mina dos Matarelli) B Mitogoniella mucuri (Alagoa: Túnel do Garrafão) C Mitobatula sp. 1 (Alagoa: Mina da Companhia) D Goniosoma vatrax (Nova Lima: Mina de Capão Xavier).
Figure 3 from: de Ázara LN, Bernardi LFO, Ferreira RL (2016) The first survey on harvestmen in Brazilian artificial cavities, with notes on distribution and natural history. Subterranean Biology 17: 31-53. https://doi.org/10.3897/subtbiol.17.6762
Figure 3 - Gryne perlata A Individual inside the mine Túnel dos Meninos II, Padre Paraíso B aggregation of individuals in the same cavity.
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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.
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.