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806 results for “cavities”

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zenodo28/100

FIGURE 6 in A new species of Domene Fauvel, 1873 (Coleoptera: Staphylinidae: Paederinae) from a granitic cavity in Serra da Estrela (Portugal)

FIGURE 6. Genital segment of Domene viriatoi n. sp. (ventral view): (a), male; (b), female.

opennotspecifiedDec 2015View details →
zenodo28/100

FIGURE 1 in A new species of Domene Fauvel, 1873 (Coleoptera: Staphylinidae: Paederinae) from a granitic cavity in Serra da Estrela (Portugal)

FIGURE 1. Buraco da Moura topographic profile showing the pitfall trapping locations.

opennotspecifiedDec 2015View details →
zenodo28/100

Figs. 1–2. Strigister tecolotito. 1 in A New Genus and Species of North American Exosternini Associated with Cavity-Nesting Owls and a Reassignment ofPhelister simoniLewis (Coleoptera: Histeridae: Histerinae)

Figs. 1–2. Strigister tecolotito. 1) Antennal club; 2) Prosternum, ventrolateral view.

opennotspecifiedDec 2013View details →
zenodo28/100

CANDIDASIS. APPEARANCE IN THE ORAL CAVITY. INSPECTION METHODS. MODERN MEDICINES. PROPHYLAXIS

Open the record for dataset details and reuse information.

opencc-by-4.0Dec 2023View details →
zenodo28/100

Supplementary material 5 from: Timm L, Schaal J, Sann M (2024) A DNA-barcoding-based approach to quantitatively investigate larval food resources of cavity-nesting wasps from trap nests. Journal of Hymenoptera Research 97: 45-56. https://doi.org/10.3897/jhr.97.117410

Trap nests locations

opencc-zeroJan 2024View details →
zenodo28/100

Supplementary material 4 from: Timm L, Schaal J, Sann M (2024) A DNA-barcoding-based approach to quantitatively investigate larval food resources of cavity-nesting wasps from trap nests. Journal of Hymenoptera Research 97: 45-56. https://doi.org/10.3897/jhr.97.117410

Information on sampling sites

opencc-zeroJan 2024View details →
zenodo28/100

Supplementary material 1 from: Timm L, Schaal J, Sann M (2024) A DNA-barcoding-based approach to quantitatively investigate larval food resources of cavity-nesting wasps from trap nests. Journal of Hymenoptera Research 97: 45-56. https://doi.org/10.3897/jhr.97.117410

PCR Conditions

opencc-zeroJan 2024View details →
zenodo28/100

Supplementary material 2 from: Timm L, Schaal J, Sann M (2024) A DNA-barcoding-based approach to quantitatively investigate larval food resources of cavity-nesting wasps from trap nests. Journal of Hymenoptera Research 97: 45-56. https://doi.org/10.3897/jhr.97.117410

Barcode and nest information

opencc-zeroJan 2024View details →
zenodo28/100

Supplementary material 3 from: Timm L, Schaal J, Sann M (2024) A DNA-barcoding-based approach to quantitatively investigate larval food resources of cavity-nesting wasps from trap nests. Journal of Hymenoptera Research 97: 45-56. https://doi.org/10.3897/jhr.97.117410

Infos on arthopods

opencc-zeroJan 2024View details →
zenodo28/100

Figure 2 from: Timm L, Schaal J, Sann M (2024) A DNA-barcoding-based approach to quantitatively investigate larval food resources of cavity-nesting wasps from trap nests. Journal of Hymenoptera Research 97: 45-56. https://doi.org/10.3897/jhr.97.117410

Figure 2 Tri-trophic interaction networks of the studied vespid and apoid wasp species comprising identified prey species and natural enemies. Interaction networks were conducted for the A spider-hunting apoid wasp T. clavicerumB aphid-hunting apoid wasp species P. corniger, P. gracilis and P. fuscipennis and CLepidoptera-hunting vespid wasp A. nigricornis, cricket-hunting apoid wasps I. mexicana and weevil-hunting vespid wasp M. parvulus. Yellow boxes represent the nest cell and the respective wasp larva, blue boxes the natural enemies and green boxes the prey species and the number of prey individuals per species per nest cell. Boxes with no number represent one individual only. The natural enemy Pronotalia sp. was not counted due to a high and randomely distributed number of individuals in the nest cell (> 40). Connections of nests and prey species are marked with grey bars.

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

Figure 1 from: Timm L, Schaal J, Sann M (2024) A DNA-barcoding-based approach to quantitatively investigate larval food resources of cavity-nesting wasps from trap nests. Journal of Hymenoptera Research 97: 45-56. https://doi.org/10.3897/jhr.97.117410

Figure 1 Nesting site and sample collection procedure: A example of a trap nest placed in the Botanical Garden of the University of Hohenheim, Stuttgart, Germany B, C nests of Passaloecus gracilis and Isodontia mexicana. One nest comprises several nest cells, which are separated by a given nesting material e.g. silky membran (B) or dry grass fragments (C) E morphotyped aphids F morphotyped spiders.

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

"Contrasting responses to increasing dissolved iron on photosynthesis and O2 availability in the gastric cavity of two Mediterranean corals." Dataset

<p>Dataset of iron levels, coral metabolic rates, PAM, Oxygen microprofiles&nbsp;</p>

opencc-by-4.0Nov 2023View details →
zenodo28/100

CHANGES IN THE ORAL CAVITY CAUSED BY IODINE DEFICIENCY

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opencc-by-4.0Nov 2024View details →
dryad28/100

Data for: Nest cavity reuse by the cooperatively breeding Acorn Woodpecker

<p><span><span><span><span><span><span><span><span><span><span><span>Although primary cavity-nesting species are capable of excavating new cavities, they often reuse old ones. To determine potential factors driving such reuse, we studied nest-cavity reuse in the Acorn Woodpecker (<i>Melanerpes formicivorus</i>), a cooperative breeding species that reuses old cavities for 57.2% of nests at Hastings Reservation in central coastal California, USA. We found no evidence for significant fitness costs or benefits of cavity reuse compared to using newly constructed cavities. In contrast, several lines of evidence supported a role for constraints on both cavity reuse and on new cavity construction. The main constraint on reuse was cavities failing to survive from one year to the next, usually because the limb fell apart, filled with water, or was usurped by another species. Evidence that constraints on new cavity construction may be important included more frequent cavity reuse when groups renested and use of artificial cavities when they were experimentally provided. Nest-cavity reuse in this population appears to be driven primarily by constraints, including the energetic costs and time required to excavate a new cavity, rather than fitness consequences, even though Acorn Woodpeckers regularly excavate small holes in trees for acorn storage and the energetic costs of new cavity construction are apparently insufficient to significantly depress reproductive success. Constraints play a significant role in cavity reuse and may affect both the intraspecific and interspecific frequency of cavity reuse among facultative excavating species.</span></span></span></span></span></span></span></span></span></span></span></p>

opencc-zeroNov 2021View details →
zenodo28/100

FIGURE 2 in Redescription of the external and internal oral cavity morphology of the tadpole of Ceratophrys aurita (Raddi, 1823) (Anura: Ceratophryidae) from the Caatinga domain, Bahia, northeast Brazil

FIGURE 2. Ceratophrys aurita tadpole at Stage 28. (A) Lateral, (B) dorsal view and (C) oral disc.

opennotspecifiedApr 2022View details →
zenodo28/100

Text-fig. 4. SRXTM images of Miranthus elegans gen. et sp. nov.; Mira locality, Portugal. a, b: Transverse (a) and longitudinal (b) sections of flower showing the ovary wall (ow) and numerous ovules (ov) borne on the mushroom-shaped central globose placenta (pl, blue); placenta shown as a voltex rendering added to orthoslices; note the large openings in the floral tissue (asterisks) interpreted as schizogenous secretory cavities. c, d: Longitudinal (c) and transverse (d) sections of flower (c, volume rendering cut between orthoslice yz0970-1005; d, volume rendering cut between orthoslice xy0780-0820) showing semiinferior ovary (ow, ovary wall) with sepals inserted at the rim of the hypanthium, central column (cc) with mushroom-shaped globose placenta (pl) bearing numerous ovules (ov). Specimens, Mira 100-S153146 (a, b), Mira 100-S170155 (c, d, holotype). Scale bars = 600 µm (a–d). in Early Flowers Of Primuloid Ericales From The Late Cretaceous Of Portugal And Their Ecological And Phytogeographic Implications

Text-fig. 4. SRXTM images of Miranthus elegans gen. et sp. nov.; Mira locality, Portugal. a, b: Transverse (a) and longitudinal (b) sections of flower showing the ovary wall (ow) and numerous ovules (ov) borne on the mushroom-shaped central globose placenta (pl, blue); placenta shown as a voltex rendering added to orthoslices; note the large openings in the floral tissue (asterisks) interpreted as schizogenous secretory cavities. c, d: Longitudinal (c) and transverse (d) sections of flower (c, volume rendering cut between orthoslice yz0970-1005; d, volume rendering cut between orthoslice xy0780-0820) showing semiinferior ovary (ow, ovary wall) with sepals inserted at the rim of the hypanthium, central column (cc) with mushroom-shaped globose placenta (pl) bearing numerous ovules (ov). Specimens, Mira 100-S153146 (a, b), Mira 100-S170155 (c, d, holotype). Scale bars = 600 µm (a–d).

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

Text-fig. 5. Anacardiaceae (a–m), Burseraceae (n–q). Scale bars = 1 cm. a–f: Pentoperculum sp. a–c: USNM PAL 772360. a: Lateral view of endocarp, apex up; three germination valves visible, the central clearly displaying the bipartite nature of the valve, reflected light, palladium coated. b: Apical view displaying six locules, with two preserved germination valves at the lower left, reflected light, palladium coated. c: Basal view of the endocarp, the locules suggested by swellings; note point of attachment, micro-CT scan surface rendering. d–f: Pentoperculum sp. USNM PAL 772359, reflected light, palladium coated. d: Lateral view of a probable 6-loculed endocarp, apex up; a single intact germination valve in the center, displaying the central lineation that divides it in two. e: Apical view; two bi-partite germination valves are visible, indicated by arrows to the middle cleavage line of two of the valves. f: Basal view, the locules suggested by the undulations in the margin. g–i: Indet. Spondioideae. USNM PAL 772358, reflected light, palladium coated. g: Lateral view of multi-locular endocarp, apex up. h: Apical view showing finely punctuate surface and peripheral locule cavities. i: Basal view. j–m: Cf. Pleiogynium USNM PAL 772357. j: Lateral view of the multi-locular endocarp, apex up; note intact germination valve on left and exposed locule facing the viewer, micro-CT scan surface rendering. k: Lateral view, rotated about 30° from (j), showing three exposed locules, reflected light, palladium coated; note bipartite locule lining at center. l: Apical view of the multilocular endocarp; the locule with intact germination valve at the upper right, reflected light, palladium coated. Arrows to each locule. m: Basal view showing central point of attachment and prominent radiating ridges aligned with the locules, micro-CT scan surface rendering. n–q: Canarium, USNM PAL 772361. Scale bar = 1 cm. n: Lateral view of endocarp directly facing one germination valve flanked by two strong ridges; apex up; specimen coated in sodium nitrate and photographed by R. A. Scott. o: Lateral view facing one of the three pronounced ridges, flanked to the left and right by two germination valves; apex up. p: Apical view displaying the three strong ridges, arching over the apex and flanking three deep embayments, covered with germination valves. q: Basal view, the three ridges being less pronounced. o–q: Reflected light, palladium coated. in The Early Middle Eocene Wagon Bed Carpoflora Of Central Wyoming, U.S.A.

Text-fig. 5. Anacardiaceae (a–m), Burseraceae (n–q). Scale bars = 1 cm. a–f: Pentoperculum sp. a–c: USNM PAL 772360. a: Lateral view of endocarp, apex up; three germination valves visible, the central clearly displaying the bipartite nature of the valve, reflected light, palladium coated. b: Apical view displaying six locules, with two preserved germination valves at the lower left, reflected light, palladium coated. c: Basal view of the endocarp, the locules suggested by swellings; note point of attachment, micro-CT scan surface rendering. d–f: Pentoperculum sp. USNM PAL 772359, reflected light, palladium coated. d: Lateral view of a probable 6-loculed endocarp, apex up; a single intact germination valve in the center, displaying the central lineation that divides it in two. e: Apical view; two bi-partite germination valves are visible, indicated by arrows to the middle cleavage line of two of the valves. f: Basal view, the locules suggested by the undulations in the margin. g–i: Indet. Spondioideae. USNM PAL 772358, reflected light, palladium coated. g: Lateral view of multi-locular endocarp, apex up. h: Apical view showing finely punctuate surface and peripheral locule cavities. i: Basal view. j–m: Cf. Pleiogynium USNM PAL 772357. j: Lateral view of the multi-locular endocarp, apex up; note intact germination valve on left and exposed locule facing the viewer, micro-CT scan surface rendering. k: Lateral view, rotated about 30° from (j), showing three exposed locules, reflected light, palladium coated; note bipartite locule lining at center. l: Apical view of the multilocular endocarp; the locule with intact germination valve at the upper right, reflected light, palladium coated. Arrows to each locule. m: Basal view showing central point of attachment and prominent radiating ridges aligned with the locules, micro-CT scan surface rendering. n–q: Canarium, USNM PAL 772361. Scale bar = 1 cm. n: Lateral view of endocarp directly facing one germination valve flanked by two strong ridges; apex up; specimen coated in sodium nitrate and photographed by R. A. Scott. o: Lateral view facing one of the three pronounced ridges, flanked to the left and right by two germination valves; apex up. p: Apical view displaying the three strong ridges, arching over the apex and flanking three deep embayments, covered with germination valves. q: Basal view, the three ridges being less pronounced. o–q: Reflected light, palladium coated.

opencc-by-4.0Aug 2022View details →
zenodo28/100

Rotational Superradiance in a Time-Reversal Symmetry-Broken Quantum Gas inside an Optical Cavity

<p>Animations of the real-time dynamics for ramping the pump strength and synthteic magnetic field.</p>

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

Photon number trajectories for "Monitoring the energy of a cavity by observing the emission of a repeatedly excited qubit"

<p>Includes 1000 photon number trajectories, obtained the same way as in Fig. 3c of the article.</p>

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

Data for "A quantum-network register assembled with optical tweezers in an optical cavity"

Open the record for dataset details and reuse information.

opencc-by-4.0Jul 2024View details →

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Last verified 2026-04-30Open record

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Last verified 2026-04-29Open record