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35 results for “fruit feeding”

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dryad32/100

Fruit-feeding butterflies of Nyungwe National Park, Rwanda

<p>A study was conducted in Nyungwe National Park, Rwanda from October 2019 to August 2020. The study aimed at documenting the diversity and distribution of fruit-feeding butterflies across an elevation gradient in Nyungwe National Park. Sampling was conducted seasonally using fruit-bated traps. Higher species richness was documented at low altitudes and decline with increasing elevation. </p>

opencc-zeroMar 2022View details →
zenodo32/100

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 &amp; 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 &amp; Hill (1992), Dang Huy Huynh et al. (1994), Ellerman (1941), Marshall (1977b), Musser &amp; Carleton (2005), Osgood (1932), Phillips (1980), Wang Yingxiang (2003).

opennotspecifiedNov 2017View details →
zenodo32/100

Lophuromys medicaudatus, L. woosnami, and L. luteogaster are in subgenus Kivumys and woosnami species group. Monotypic. Distribution. Endemic to the Albertine Rift, occurring around Lake Kivu in E DR Congo and Rwanda and SW Uganda (Bwindi). Descriptive notes. Head—body 92-112 mm, tail 73-95 mm, ear 15-19 mm, hindfoot 18-23 mm; weight 29-43 g. Similar to other species in subgenus Kivumys, the Western Rift Brush-furred Rat has unspeckled pelage, and tail ¢.85% of head-body length. Dorsum is uniform dark brown-olive, and venter is orange. Females have three pairs of mammae. Habitat. Mountain swamps and mountain forests at elevations of 1850-2500 m. Food and Feeding. The Western Rift Brush-furred Rat is omnivorous; diets contain 30-100% arthropods, mollusks, seeds, and fruits. Breeding. Female Western Rift Brush-furred Rats can have 1-2 embryos. Pregnant females were observed in February, April, and July. Activity patterns. The Western Rift Brush-furred Rat is terrestrial. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Vulnerable on The IUCN Red List. The Western Rift Brush-furred Rat has never been found in modified secondary environment and is quite rare. Bibliography. Dieterlen (1976b, 1987 2013g), Kasangaki et al. (2003), Verheyen et al. (1996). in Muridae

Lophuromys medicaudatus, L. woosnami, and L. luteogaster are in subgenus Kivumys and woosnami species group. Monotypic. Distribution. Endemic to the Albertine Rift, occurring around Lake Kivu in E DR Congo and Rwanda and SW Uganda (Bwindi). Descriptive notes. Head—body 92-112 mm, tail 73-95 mm, ear 15-19 mm, hindfoot 18-23 mm; weight 29-43 g. Similar to other species in subgenus Kivumys, the Western Rift Brush-furred Rat has unspeckled pelage, and tail ¢.85% of head-body length. Dorsum is uniform dark brown-olive, and venter is orange. Females have three pairs of mammae. Habitat. Mountain swamps and mountain forests at elevations of 1850-2500 m. Food and Feeding. The Western Rift Brush-furred Rat is omnivorous; diets contain 30-100% arthropods, mollusks, seeds, and fruits. Breeding. Female Western Rift Brush-furred Rats can have 1-2 embryos. Pregnant females were observed in February, April, and July. Activity patterns. The Western Rift Brush-furred Rat is terrestrial. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Vulnerable on The IUCN Red List. The Western Rift Brush-furred Rat has never been found in modified secondary environment and is quite rare. Bibliography. Dieterlen (1976b, 1987 2013g), Kasangaki et al. (2003), Verheyen et al. (1996).

opennotspecifiedNov 2017View details →
dryad32/100

Data for: Aridity and chronic anthropogenic disturbance as organizing forces of fruit-feeding butterfly assemblages in a Caatinga dry forest

<p><span>Anthropogenic disturbances and climate change are expected to reorganize biodiversity on multiple ecological levels from populations to ecosystems, especially in arid and semiarid regions due to environmental filtering imposed by water stress. This paper examines the individual and combined effects of chronic anthropogenic disturbance and increased aridity on the structure of fruit-feeding butterfly assemblages in a human-modified landscape of Caatinga dry forest, in the northeast of Brazil. Butterflies were recorded monthly across old-growth forest stands and their assemblages were described in terms of taxonomic and functional community-level attributes confronted with different levels of chronic disturbance and aridity. Butterfly assemblages were species-poor but had high species replacement (turnover) along both the chronic disturbance and aridity gradients. We observed a negative effect of aridity on the alpha and beta diversity of butterfly assemblages. Butterfly assemblages across forest stands exposed to high levels of chronic disturbance and aridity had a nested structure. Functional diversity (Rao's Q) and the community-weighted means (CWM) of ocellus-bearing species and monocot-feeding larvae were negatively and positively affected by increased aridity and chronic disturbance, respectively. Our findings suggest that aridity and its combination with chronic disturbance have a drastic effect on the structure of butterfly assemblages in the Caatinga dry forest. These findings highlight that rainfall and chronic disturbances as major drivers of biological reorganization in human-modified landscapes. As aridity increases, Caatinga tends to support taxonomically and functionally impoverished and highly distorted assemblages.</span></p>

opencc-zeroNov 2022View details →
dryad32/100

Data for: Aridity and chronic anthropogenic disturbance as organizing forces of fruit-feeding butterfly assemblages in a Caatinga dry forest

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publicNov 2022View details →
dryad32/100

Fruit-feeding butterflies of Nyungwe National Park, Rwanda

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publicMar 2022View details →
dryad28/100

Data from: Enhanced yeast feeding following mating facilitates control of the invasive fruit pest Drosophila suzukii

The highly invasive spotted wing Drosophila Drosophila suzukii is a key pest of soft fruit and berries in Europe and North America, and development of control techniques is an urgent research challenge. Drosophila suzukii is widely associated with the yeast Hanseniaspora uvarum. Yeasts are symbionts of drosophilid flies and communicate with insects through volatile metabolites for spore dispersal. Accordingly, yeasts and behaviour-modifying chemicals produced by yeasts are prospective tools for environmentally sound insect management. We first bioassayed flight attraction, feeding and oviposition of D. suzukii females in response to H. uvarum yeast and blueberries, which are a preferred host fruit. We then investigated the combined effect of yeast and insecticide on adult female oviposition behaviour and mortality towards the development of a yeast-based control method. Following mating, attraction of female flies to blueberry and yeast odour cues was strongly enhanced. Yeast feeding significantly increased in mated females, while yeast did not increase oviposition on blueberries. This observation suggests that mated flies become attracted to yeast for feeding and to fruit for egg laying. A combined feeding–oviposition assay demonstrated different roles and interference between yeast and fruit stimuli: during the day after mating, females laid fewer eggs when yeast was available. The post-mating yeast-feeding response is an opportunity for the development of an attract-and-kill technique for population control of D. suzukii. Exposing flies to a blend of yeast and insecticide reduced oviposition and greatly enhanced adult fly mortality compared with an insecticide treatment alone. Synthesis and applications. Mated females are the key life stage for Drosophila suzukii population control. Egg-laying females perforate fruit skin and fungal infestations ensue, even when eggs and larvae are killed off by insecticide sprays. Behaviour-modifying chemicals, including yeast metabolites, enable environmentally safe insect management via manipulation of olfactory-mediated reproductive behaviour. Our results highlight that yeast and yeast semiochemicals hold potential for D. suzukii management and that response modulation to olfactory stimuli following mating is a vital element for the development of D. suzukii control methods. Yeast feeding is enhanced in mated D. suzukii females, and this change in post-mating behaviour can be exploited by an attract-and-kill strategy, combining a fly-associated yeast with an insecticide. Furthermore, using the D. suzukii yeast mutualist, H. uvarum, may reduce non-target effects and increase species specificity, which further contributes to the development of an efficient and safe control method.

opencc-zeroDec 2015View details →
zenodo28/100

Fig. 2 in Stator Huautlae, a New Species From Mexico Feeding in Fruits of Sage (Lamiaceae), a New Host Family From the New World for Bruchidae (Coleoptera)

Fig. 2. Lateral aspect of Stator huautlae.

opennotspecifiedJun 2004View details →
zenodo28/100

Fig. 1 in Stator Huautlae, a New Species From Mexico Feeding in Fruits of Sage (Lamiaceae), a New Host Family From the New World for Bruchidae (Coleoptera)

Fig. 1. Dorsal aspect of Stator huautlae.

opennotspecifiedJun 2004View details →
zenodo28/100

Fig. 5 in Stator Huautlae, a New Species From Mexico Feeding in Fruits of Sage (Lamiaceae), a New Host Family From the New World for Bruchidae (Coleoptera)

Fig. 5. Egg of Stator huautlae glued to the surface of a nutlet of Salvia sessei.

opennotspecifiedJun 2004View details →
zenodo28/100

FIGURE 2 in Species diversity and community structure of fruit-feeding butterflies (Lepidoptera: Nymphalidae) in an eastern amazonian forest

FIGURE 2: Each sampling site was composed of one trail and three transects to the interior of the forest. Points represent cylindrical traps baited with a mix of banana and sugarcane juice.

opencc-by-4.0Dec 2017View details →
zenodo28/100

Fig. 5. A in Temporal dynamics of fruit-feeding butterflies (Lepidoptera: Nymphalidae) in two habitats in a seasonal Brazilian environment

Fig. 5. A) Temporal variation in Nymphalidae species richness captured in the dry and wet seasons and in the 2 transitional periods between those seasons, wet to dry (T.wd) and dry to wet (T.dw), in savanna (Cerrado sensu stricto, ss) and gallery forest habitats in the Fazenda Água Limpa and the Reserva Ecológica do Roncador, Brasília, DF. The rarefaction curves compare the 4 climatic periods—dry (black triangles) and wet (black circles) seasons, and the transitional periods from wet to dry (T.wd, white circles) and from dry to wet (T.dw, white triangles)—in B) gallery forest and C) savanna separately.

opencc-by-4.0Nov 2015View details →
dryad28/100

Data from: Enhanced yeast feeding following mating facilitates control of the invasive fruit pest Drosophila suzukii

Open the record for dataset details and reuse information.

publicApr 2017View details →
zenodo24/100

Figure 1 in Halyomorpha halys Stål, (Hemiptera:Pentatomidae) feeding effects on some agricultural fruits in Georgia

Figure 1. Damage (%) caused by BMSB feeding on fully grown hazelnut kernels in Samegrelo, 2019.

opencc-by-4.0Apr 2022View details →
zenodo16/100

F in Finding the host tree species of Notiobia nebrioides Perty (Coleoptera, Carabidae), a member of the seed-feeding guild at fruit falls in Amazonian non-inundated lowland rainforest

F. 1. Food niches for the Notiobia species community at Reserva Ducke, Central Amazonia.

opennotspecifiedApr 2003View details →

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Last verified 2026-04-29Open record