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266 results for “shelter”
Fig 1 in Amphibious Shelter-Builder Oniscidea Species from the New World with Description of a New Subfamily
Fig 1. Iuiuniscus iuiuensis gen. et sP. nov. (HolotyPe, UFBA 1603). (A) First antenna, (B) Second antenna, (C) Left mandible, (D) Right mandible, (E) First maxilla, (F) Second maxilla, (G) Maxilliped. Scale bars: 0.1 mm for A; 1.0 mm for B; 0.2 mm for the remainder. doi:10.1371/journal.pone.0115021.g001
Fig 3 in Amphibious Shelter-Builder Oniscidea Species from the New World with Description of a New Subfamily
Fig 3. Iuiuniscus iuiuensis gen. et sP. nov. (HolotyPe, UFBA 1603). (A) Pleopod 1, (C) Pleopod 2. (Paratype, female, UFBA 1604). (B) Pleopod 1, (D) Pleopod 2. Scale bars: 0.5 mm. doi:10.1371/journal.pone.0115021.g003
Figure 1 in Occupation dynamics and nesting behaviours of Xylocopa frontalis (Olivier) (Hymenoptera: Apidae) in artificial shelters
Figure 1. Temporal variation of the number of Xylocopa frontalis nesting females and the number of brood cells produced in the shelters at the Panga Ecological Station (PES) and at the Água Limpa Experimental Farm (ALEF) from April 2012 to March 2013.
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925). in Muridae
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925).
Rock Shelter Cup Marks in Gleann Da-Eig
This cup-marked slab of schist is situated underneath a hidden rock shelter in Gleann Da-Eig, a side valley of Glen Lyon. It was found by George Currie in 2006 and probably not visited since until I uncovered it again in July 2022. The overhanging rock is obviously much used as a shelter to this day, but for the local sheep since the slab was buried beneath a good covering of compacted sheep....err...manure. Source: Objaverse 1.0 / Sketchfab
WWII RAF Airfield Blast Shelter
One of the surviving RAF Airfield blast shelters from RAF Ibsley in the New Forest. The site is in dense woodland and we are working with the landowner to clear and conserve the strucutres. Due to the vegetation this before model has a few holes in, but was a quick test using a mobile phone. Source: Objaverse 1.0 / Sketchfab
Fate Bell Shelter
Seminole Canyon State Park, Texas. Source: Objaverse 1.0 / Sketchfab
Temporal Dynamics and Demographic Profiles: Evaluating the Cultural Impact of Public Engagements with Civil War Shelters in Alicante (Spain)
<p>In the context of sustainable tourism, understanding visitors' needs and preferences is crucial for planning effective strategies that promote the conservation of historical and cultural heritage. In this regard, the quantitative analysis of survey results from visitors to Civil War air-raid shelters in Alicante, Spain, emerges as a valuable tool for gaining detailed insights that enable the planning of specific visits and events. This paper aims to explore the significance of using quantitative data in developing strategies for sustainable tourism within this particular context.</p>
Figure 3. A in Making shelter for enemies: parasitoid-induced shelter-building behaviour in Paraponyx stagnalis
Figure 3. A pictorial representation of the Paraponyx stagnalis life cycle. (a) Eggs are laid on the abaxial side of the leaf. (b) Newly emerged first-instar larvae are feeding on the leaf tissue. (c,d) Larvae making the leaf shelter. (e) Folded leaf case in the rice leaf. (f) Tubular cases fall off the rice plant, floating on the water. (g) The rice case worm uses its legs to climb up adjacent plants. (h) Caterpillars feed on leaves. (i) Pupae adhere to the culms of rice paddy saplings via the lateral border of the cases, slightly above the water surface.
Figure 2 in Making shelter for enemies: parasitoid-induced shelter-building behaviour in Paraponyx stagnalis
Figure 2. Pictorial representation of the process of formation of a normal leaf shelter: (a) first leaf slit made by the first-instar rice case worm larva; (b) making of the second slit; (c) removal of the leaf tip, and rolling of the leaf portion between the first and second slits; (d) detachment of the tubular case from the remaining leaf. Tthe types of parasitised larval leaf shelter: Type 1 = folding of the leaf portion above the first leaf slit; Type 2 = folding of the leaf portion between the first and second cut; and Type 3 = removal of the leaf portion above the first cut and folding the leaf between the two leaf slits.
Figure 7 in Making shelter for enemies: parasitoid-induced shelter-building behaviour in Paraponyx stagnalis
Figure 7. Primary parasitoid: (a) Apanteles species. Hyperparasitoids: (b) Paraphylax species. (c) Elasmus species.
Figure 5 in Making shelter for enemies: parasitoid-induced shelter-building behaviour in Paraponyx stagnalis
Figure 5. Biology of Apanteles species. (a) Parasitoid larva near the host (Paraponyx stagnalis) larval remnant. (b) Parasitoid pupa with an emergence hole. (c) Parasitoid cocoon shelter in the rice leaf. (d) Parasitised P. stagnalis larval shelter in grass species Digitaria. (e) Parasitised rice case worm leaf shelter.
Figure 6 in Making shelter for enemies: parasitoid-induced shelter-building behaviour in Paraponyx stagnalis
Figure 6. Leaf shelter of Paraponyx stagnalis. (a) Tubular case of late-instar larva. (b,c) Tubular cases of early-instar larvae. (d) Caterpillar making leaf shelter. (e,f) Caterpillars' bright brownish-orange head protruding from the tubular case. (g) Silk covers the case's interior, storing a small layer of water.
Figure 4 in Making shelter for enemies: parasitoid-induced shelter-building behaviour in Paraponyx stagnalis
Figure 4. Biology of Paraponyx stagnalis. (a) Unparasitised late-instar P. stagnalis larva in a cut-open case. (b) Normal tubular case of P. stagnalis. (c) Newly formed P. stagnalis pupa in a cut-open case. (d) P. stagnalis pupa within the silken cocoon. (d) Adult P. stagnalis.
FIGURE 43. Penultimate instar caterpillar constructing shelter, collected 1–2 Apr 1990 in Observations on the Biology of Afrotropical Hesperiidae (Lepidoptera). Part 5. Hesperiinae incertae sedis: Dicotyledon Feeders
FIGURE 43. Penultimate instar caterpillar constructing shelter, collected 1–2 Apr 1990 on unidentified sapling, Lower Meru Forest; photographed 2 Apr 1990; moulted 4–6 Apr; 18mm; 90/32G.
FIGURE 6 in Immature stages, new host plant records and shelter structures of Troyus phyllides (Röber, 1925) and Thoon ponka Evans, 1955 in the Peruvian Amazon (Lepidoptera Hesperiidae: Hesperiinae: Hesperiini)
FIGURE 6. The host plants, Pariana sp. and Pariana lunata, and illustrations of the shelter structures of each immature stage of Thoon ponka: a) close-up view of Pariana sp. stem; b) small Pariana sp. plant; c) Pariana sp. plants in situ; d) view of Pariana lunata leaves with inflorescence; e) close-up view of inflorescence; f) Pariana lunata plant in situ; g) shelter structure during the first instar; h) shelter structure during the second and third instars; i) shelter structure during the fourth instar; j) shelter structure during the fifth instar.
FIGURE 4 in Immature stages, new host plant records and shelter structures of Troyus phyllides (Röber, 1925) and Thoon ponka Evans, 1955 in the Peruvian Amazon (Lepidoptera Hesperiidae: Hesperiinae: Hesperiini)
FIGURE 4. Thoon ponka life stages: a) egg in dorsal and lateral view (photo of 2021-FLP-IMM-0049); b) first instar in dorsolateral view (photo of 2021-FLP-IMM-0049); c) second instar in lateral view (photo of 2021-FLP-IMM-0049); d) third instar in lateral view (photo of 2021-FLP-IMM-0281); e) fourth instar in lateral view (photo of 2021-FLP-IMM-0049); f) fifth instar in lateral view (photo of 2021-FLP-IMM-0281); g) pupa in dorsal view (photo of 2021-FLP-IMM-0281); h) pupa in ventral view (photo of 2021-FLP-IMM-0281); i) adult in dorsal and ventral view (photo of 2021-FLP-IMM-0049).
FIGURE 3 in Immature stages, new host plant records and shelter structures of Troyus phyllides (Röber, 1925) and Thoon ponka Evans, 1955 in the Peruvian Amazon (Lepidoptera Hesperiidae: Hesperiinae: Hesperiini)
FIGURE 3. The host plant, Lasiacis ligulata, and illustrations of the shelter structures of each immature stage of Troyus phyllides: a) close-up view of leaves; b) close-up view of inflorescence; c) plant in situ; d) shelter structure during the first instar; e) shelter structure during the second instar; f) shelter structure during the third instar; g) shelter structure during the fourth instar; h) shelter structure during the fifth instar.
FIGURE 2 in Immature stages, new host plant records and shelter structures of Troyus phyllides (Röber, 1925) and Thoon ponka Evans, 1955 in the Peruvian Amazon (Lepidoptera Hesperiidae: Hesperiinae: Hesperiini)
FIGURE 2. Head capsule illustrations of Troyus phyllides (based on 2021-FLP-IMM-0366): a) first instar in frontal view; b) second instar in frontal view; c) third instar in frontal view; d) fourth instar in frontal view; e) fifth instar in frontal view.
FIGURE 1 in Immature stages, new host plant records and shelter structures of Troyus phyllides (Röber, 1925) and Thoon ponka Evans, 1955 in the Peruvian Amazon (Lepidoptera Hesperiidae: Hesperiinae: Hesperiini)
FIGURE 1. Troyus phyllides life stages: a) egg in dorsal and lateral view (photo of 2021-FLP-IMM-0116); b) first instar in lateral view (photo of 2021-FLP-IMM-0366); c) second instar in lateral view, note that the larva had recently molted and the previous head capsule is visible nearby (photo of 2021-FLP-IMM-0367); d) third instar in lateral view (photo of 2021-FLP- IMM-0367); e) fourth instar in lateral view (photo of 2021-FLP-IMM-0366); f) fifth instar in lateral view (photo of 2021-FLP- IMM-0366); g) prepupa in lateral view (photo of 2021-FLP-IMM-0116); h, i) pupa in ventral and dorsal view (photo of 2021- FLP-IMM-0366); j) adult in dorsal and ventral view (photo of 2021-FLP-IMM-0116).
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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)
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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.