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39 results for “Nest building”
Deccan region, Madras, India. Genus Vandeleuria is masculine, so widely used specific name oleracea has been changed for gender agreement. Vandeleuria oleraceusis possibly a composite of species. Polytypic, but subspecific taxonomy requires reassessment. Distribution. Widespread in S Asia (India, Nepal, Bhutan, Bangladesh, and Sri Lan-ka), S China (W & S Yunnan), and mainland SE Asia N of the Isthmus of Kra. Descriptive notes. Head-body 68 mm, tail 105 mm, ear 13 mm, hindfoot 17 mm; weight 10 g. The Indomalayan Long-tailed Climbing Mouse is small, with flat nail on outer finger and outertoe; tail is slender, brown, twice as long as head-body length, and lacks distal tuft. Dorsal pelageis silky and salmon in color; venter is white, with fulvous hues. Habitat. Tall cane and tangled vines in primary and secondary forest such as bamboo forest, moist deciduous forest, temperate forests, montane wet zone, and disturbed secondary forests, and perhaps agricultural areas at elevations of 150-1500 m. Food and Feeding. Indomalayan [Long-tailed Climbing Mice eat fruits, buds, and flowers. Breeding. Litters of the Indomalayan Long-tailed Climbing Mouse have 3-6 young. Activity patterns. Indomalayan Long-tailed Climbing Mice are arboreal and nocturnal, although one individual was caught duringthe day. Movements, Home range and Social organization. Indomalayan Long-tailed Climbing Mice build nests in tall bushes or cane to rear their young. Status and Conservation. Classified as Least Concern on The IUCN Red Last (as V. olacea). The Indomalayan Long-tailed Climbing Mouse occurs in several habitats and a wide distribution that includes national parks. Further taxonomical studies are required to assess conservation status ofthis potentially diverse species complex. Bibliography. Corbet & Hill (1992), Dang Huy Huynh et al. (1994), Ellerman (1941), Marshall (1977b), Musser & Carleton (2005), Osgood (1932), Phillips (1980), Wang Yingxiang (2003). in Muridae
Deccan region, Madras, India. Genus Vandeleuria is masculine, so widely used specific name oleracea has been changed for gender agreement. Vandeleuria oleraceusis possibly a composite of species. Polytypic, but subspecific taxonomy requires reassessment. Distribution. Widespread in S Asia (India, Nepal, Bhutan, Bangladesh, and Sri Lan-ka), S China (W & S Yunnan), and mainland SE Asia N of the Isthmus of Kra. Descriptive notes. Head-body 68 mm, tail 105 mm, ear 13 mm, hindfoot 17 mm; weight 10 g. The Indomalayan Long-tailed Climbing Mouse is small, with flat nail on outer finger and outertoe; tail is slender, brown, twice as long as head-body length, and lacks distal tuft. Dorsal pelageis silky and salmon in color; venter is white, with fulvous hues. Habitat. Tall cane and tangled vines in primary and secondary forest such as bamboo forest, moist deciduous forest, temperate forests, montane wet zone, and disturbed secondary forests, and perhaps agricultural areas at elevations of 150-1500 m. Food and Feeding. Indomalayan [Long-tailed Climbing Mice eat fruits, buds, and flowers. Breeding. Litters of the Indomalayan Long-tailed Climbing Mouse have 3-6 young. Activity patterns. Indomalayan Long-tailed Climbing Mice are arboreal and nocturnal, although one individual was caught duringthe day. Movements, Home range and Social organization. Indomalayan Long-tailed Climbing Mice build nests in tall bushes or cane to rear their young. Status and Conservation. Classified as Least Concern on The IUCN Red Last (as V. olacea). The Indomalayan Long-tailed Climbing Mouse occurs in several habitats and a wide distribution that includes national parks. Further taxonomical studies are required to assess conservation status ofthis potentially diverse species complex. Bibliography. Corbet & Hill (1992), Dang Huy Huynh et al. (1994), Ellerman (1941), Marshall (1977b), Musser & Carleton (2005), Osgood (1932), Phillips (1980), Wang Yingxiang (2003).
Рис. 9. Варианты размещения гнёзΑ скаΛьных гоΛубей Columba rupestris в нишах раз- Λичных строений. 1 — Δазовский район, автомобиΛьный мост через кΛюч ЗвёзΑочка, 25.05.2022, фото В. П. Шохрина; 2 — Уссурийский гороΑской округ, окрестности сеΛа НовоникоΛьск, заброшенный животновоΑческий компΛекс, 27.03.2022; 3 — Октябрьский район, окрестности сеΛа Чернятино, заброшенное зΑание, 23.04.2022; 4 — Октябрьский район, окрестности сеΛа Покровка, заброшенное зΑание 17.05.2022; 5 — там же, 17.05.2022; 6 — там же, 17.05.2022. Фото À. В. Коробова Fig. 9. Possible locations of nests of hill pigeons Columba rupestris in the niches of buildings. 1 — Lazovsky District, a road bridge over Zvezdochka Spring, 25.05.2022. Photo by V. P. Shokhrin; 2 — Ussuriysky City District, vicinity of the village of Novonikolsk, abandoned livestock facility, 27.03.2022; 3 — Oktyabrsky District, vicinity of the village of Chernyatino, abandoned building, 23.04.2022; 4 — Oktyabrsky District, vicinity of the village of Pokrovka, abandoned building, 17.05.2022; 5 — in the same place, 17.05.2022; 6 — in the same place, 17.05.2022. Photo by D. V. Korobov in About breeding biology of the hill pigeon Columba rupestris in Primorsky Krai
Рис. 9. Варианты размещения гнёзΑ скаΛьных гоΛубей Columba rupestris в нишах раз- Λичных строений. 1 — Δазовский район, автомобиΛьный мост через кΛюч ЗвёзΑочка, 25.05.2022, фото В. П. Шохрина; 2 — Уссурийский гороΑской округ, окрестности сеΛа НовоникоΛьск, заброшенный животновоΑческий компΛекс, 27.03.2022; 3 — Октябрьский район, окрестности сеΛа Чернятино, заброшенное зΑание, 23.04.2022; 4 — Октябрьский район, окрестности сеΛа Покровка, заброшенное зΑание 17.05.2022; 5 — там же, 17.05.2022; 6 — там же, 17.05.2022. Фото À. В. Коробова Fig. 9. Possible locations of nests of hill pigeons Columba rupestris in the niches of buildings. 1 — Lazovsky District, a road bridge over Zvezdochka Spring, 25.05.2022. Photo by V. P. Shokhrin; 2 — Ussuriysky City District, vicinity of the village of Novonikolsk, abandoned livestock facility, 27.03.2022; 3 — Oktyabrsky District, vicinity of the village of Chernyatino, abandoned building, 23.04.2022; 4 — Oktyabrsky District, vicinity of the village of Pokrovka, abandoned building, 17.05.2022; 5 — in the same place, 17.05.2022; 6 — in the same place, 17.05.2022. Photo by D. V. Korobov
Рис. 3. ЖиΛое зΑание, в черΑачном помещении которого гнезΑятся скаΛьные гоΛуби Columba rupestris. Октябрьский район, сеΛо Чернятино, 23.04.2022. Фото À.В. Коробова Fig. 3. A residential building with nests of hill pigeons Columba rupestris in the attic. Oktyabrsky District, Chernyatino Village, 23.04.2022. Photo by D.V. Korobov in About breeding biology of the hill pigeon Columba rupestris in Primorsky Krai
Рис. 3. ЖиΛое зΑание, в черΑачном помещении которого гнезΑятся скаΛьные гоΛуби Columba rupestris. Октябрьский район, сеΛо Чернятино, 23.04.2022. Фото À.В. Коробова Fig. 3. A residential building with nests of hill pigeons Columba rupestris in the attic. Oktyabrsky District, Chernyatino Village, 23.04.2022. Photo by D.V. Korobov
Рис. 4. НежиΛые заброшенные постройки, внутри которых гнезΑятся скаΛьные гоΛуби Columba rupestris. 1 — Уссурийский гороΑской округ, окрестности сеΛа НовоникоΛьск, 27.03.2022; 2 — Уссурийский гороΑской округ, окрестности сеΛа Монакино, 03.05.2022. Фото À. В. Коробова Fig. 4. Abandoned buildings with nests of hill pigeons Columba rupestris inside. 1 — Ussuriysky City District, vicinity of the village of Novonikolsk, 27.03.2022; 2 — Ussuriysky City District, vicinity of the village of Monakino, 03.05.2022. Photo by D. V. Korobov in About breeding biology of the hill pigeon Columba rupestris in Primorsky Krai
Рис. 4. НежиΛые заброшенные постройки, внутри которых гнезΑятся скаΛьные гоΛуби Columba rupestris. 1 — Уссурийский гороΑской округ, окрестности сеΛа НовоникоΛьск, 27.03.2022; 2 — Уссурийский гороΑской округ, окрестности сеΛа Монакино, 03.05.2022. Фото À. В. Коробова Fig. 4. Abandoned buildings with nests of hill pigeons Columba rupestris inside. 1 — Ussuriysky City District, vicinity of the village of Novonikolsk, 27.03.2022; 2 — Ussuriysky City District, vicinity of the village of Monakino, 03.05.2022. Photo by D. V. Korobov
Data from: Nest building in titmice Paridae: Selectivity in bryophyte use
<p><span>In many bird species, reproductive success is dependent on nest quality. However, detailed data on nest composition are scarce, and quantitative analyses have generally used only rough categories, without species identification. Bryophytes dominate the nests of many </span><span>passerine bird species, </span><span>but little is known about whether birds have preferences for certain species. In this study, we determined the bryophyte species composition in nests of blue tits <em>Cyanistes caeruleus</em> and great tits <em>Parus major</em> in a forest near Oslo, Norway. We also sampled the abundance of the bryophyte species in plots on the forest floor surrounding a subset of the great tit nests. Blue tits and great tits both used 15 bryophyte species as nest materials, mainly the same pleurocarpous species but in different proportions. The tits preferred highly branched bryophyte species, i.e. <em>Pleurozium schreberi</em>, <em>Rhytidiadelphus squarrosus</em> and <em>Sanionia uncinata</em>, but avoided common forest-floor bryophyte species that are sparsely branched. Great tits clearly collected bryophyte species selectively. We also found that bryophyte species content in great tit nests in the same nest box in different years was very similar. Our results also indicated that the great tits collected bryophyte nest materials close to their nests, mostly within 5 m, supporting the view that collecting nest materials is costly. We review several hypotheses to explain why the tits prefer certain species of bryophytes as nest materials. These include handling costs and their suitability as structural materials. We recommend field experiments to test specific hypotheses, and to study whether preferences are heritable.</span></p>
Data from: Gone with the rain: negative effects of rainfall on male mating success in a nest-building arachnid
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Data from: Plumage and eggshell colouration covary with the level of sex-specific parental contributions to nest building in birds
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Data from: Previous reproductive success informs nest-building decisions
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Data from: Nest building in titmice Paridae: Selectivity in bryophyte use
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Data from: Sex-specific contributions to nest building in birds
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F in Carton nest building and trophobiont manipulation in the south-east Asian ant Dolichoderus sulcaticeps (Mayr 1870) (Hymenoptera: Formicidae)
F. 6. Transporting the ball of plant material back to the nest. Photo: W. Rohe
F in Carton nest building and trophobiont manipulation in the south-east Asian ant Dolichoderus sulcaticeps (Mayr 1870) (Hymenoptera: Formicidae)
F. 7. Worker chewing the wet nest wall with her mandibles. Photo: W. Rohe
Figure 3 in Goliath frogs build nests for spawning - the reason for their gigantism?
Figure 3. Different Conraua goliath nest types. On the left side nest types 1 (a), 2 (b) and 3 (c) are sketched in top view and in cross section, respectively; on the right side examples for each nest type are illustrated; compare text for further details.
Figure 4 in Goliath frogs build nests for spawning - the reason for their gigantism?
Figure 4. Conraua goliath is heavily hunted in the region, either using fishhooks set above breeding habitats (a, c) or with traps (b).
Figure 1 in Goliath frogs build nests for spawning - the reason for their gigantism?
Figure 1. Adult Conraua goliath from Cameroon (a) and different sections of one of its habitats, the Mpoula River, Littoral District, western Cameroon (b, c).
F in Carton nest building and trophobiont manipulation in the south-east Asian ant Dolichoderus sulcaticeps (Mayr 1870) (Hymenoptera: Formicidae)
F. 5. D. sulcaticeps scratching the surface material with her mandibles as she moves backwards. Under the head is a pulpy ball of this surface material. Photo: W. Rohe
F in Carton nest building and trophobiont manipulation in the south-east Asian ant Dolichoderus sulcaticeps (Mayr 1870) (Hymenoptera: Formicidae)
F. 8. SEM picture of the nest material. No adhesive is detectable between the plant fibres, which are thoroughly interwoven. Photo: W. Rohe
F in Carton nest building and trophobiont manipulation in the south-east Asian ant Dolichoderus sulcaticeps (Mayr 1870) (Hymenoptera: Formicidae)
F. 2b. The same carton nest (see figure 2a) after eight days. Photo: W. Rohe
The metadata for the NEST building data points
<p>The metadata for the NEST datapoints</p>
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