Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
17
datasets available to search
ShareScore release 0.9.0
Dataset results
17 results for “maturation feeding”
Fig. 3 in Feeding behavior of Diaphorina citri (Hemiptera: Liviidae) and its acquisition of 'Candidatus Liberibacter asiaticus', on huanglongbing-infected Citrus reticulata leaves of several maturity stages
Fig. 3. The major EPG variables of Diaphorina citri adults feeding on citrus leaves of several maturity stages. Mean (+SE) (A) durations of pathway phase (C), xylem phase (G) and phloem phase (E1+E2) (B) durations of phloem salivation (E1), phloem ingestion (E2) and salivation before phloem ingestion (E1 before E2) (C) percentage of salivation in total phloem activities (E1/E1+E2) (D) time from start to first salivation in phloem (Time to first E1) and to the first ingestion from phloem (Time to first E2) and (E) numbers of single E1 (single salivation) and E1 followed by E2 (salivation followed by ingestion). Within the same series, means capped by the same letter are not significantly different according to Duncan's Multiple Range test (P> 0.05).
Data for: Predicting age and mass at maturity from feeding behavior and diet in M. sexta: An empirical test of a life history model
<p>Feeding for most animals involves bouts of active ingestion alternating with bouts of no ingestion. In insects, the temporal patterning of bouts varies widely with resource quality and is known to affect growth, development time, and fitness. However, the precise impacts of resource quality and feeding behavior on insect life history traits is poorly understood. To explore and better understand the connections between feeding behavior, resource quality and insect life history traits, we combined laboratory experiments with a recently proposed mechanistic model of insect growth and development for a larval herbivore, <em>Manduca sexta</em>. We ran feeding trials for 4<sup>th</sup> and 5<sup>th</sup> instar larvae across different diet types (two hostplants and artificial diet) and used these data to parameterize a joint model of age and mass at maturity that incorporates both insect feeding behavior and hormonal activity. We found that the estimated durations of both feeding and non-feeding bouts were significantly shorter on low- than on high-quality diets. We then explored how well the fitted model predicted historical out-of-sample data on age and mass of <em>M</em>.<em> sexta</em>. We found that the model accurately described qualitative outcomes for the out-of-sample data, notably that a low-quality diet results in reduced mass and later age at maturity compared to high-quality diets. Our results clearly demonstrate the importance of diet quality on multiple components of insect feeding behavior (feeding and non-feeding), and partially validate a joint model of insect life history. We discuss the implications of these findings with respect to insect herbivory and discuss ways in which our model could be improved or extended to other systems.</p>
Inclusion of Spirulina sp. (Arthospira) in the feed of Arapaima gigas (Schinz, 1822) broodstocks: effects on gonadal maturation
<p>Dataset containing information on gonadal development from a trial which tested the Inclusion of <em>Spirulina</em><strong> </strong>sp. (<em>Arthospira</em>) in the feed of <em>Arapaima gigas</em> (Schinz, 1822) broodstocks.</p>
Data for: Predicting age and mass at maturity from feeding behavior and diet in M. sexta: An empirical test of a life history model
Open the record for dataset details and reuse information.
Fig. 1 in Feeding behavior of Diaphorina citri (Hemiptera: Liviidae) and its acquisition of 'Candidatus Liberibacter asiaticus', on huanglongbing-infected Citrus reticulata leaves of several maturity stages
Fig. 1. Sketches of citrus leaves at several maturity stages.
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).
Figure 3 in Effects of sexual maturity and feeding on condition of a deep-sea flatfish, Lepidorhombus boscii, in north-eastern Mediterranean waters
Figure 3. Seasonal patterns of mean gonadosomatic factor (GSI) values for small (LTǩ110 mm), medium (111ǩLTǩ180 mm) and large (LT>181 mm) length categories of male and female four-spotted megrim in the west Aegean Sea. Vertical bars denote standard errors of the means.
Figure 7 in Effects of sexual maturity and feeding on condition of a deep-sea flatfish, Lepidorhombus boscii, in north-eastern Mediterranean waters
Figure 7. Seasonal patterns of mean stomach-somatic factor (SSI) values for small (LTǩ110 mm), medium (111ǩLTǩ180 mm) and large (LT>181 mm) length categories of male and female four-spotted megrim in the west Aegean Sea. Vertical bars denote standard errors of the means.
Figure 2 in Effects of sexual maturity and feeding on condition of a deep-sea flatfish, Lepidorhombus boscii, in north-eastern Mediterranean waters
Figure 2. Seasonal patterns of mean condition factor (K) values for small (LTǩ110 mm), medium (111ǩLTǩ180 mm) and large (LT>181 mm) length categories of male and female four-spotted megrim in the west Aegean Sea. Vertical bars denote standard errors of the means.
Figure 5 in Effects of sexual maturity and feeding on condition of a deep-sea flatfish, Lepidorhombus boscii, in north-eastern Mediterranean waters
Figure 5. Seasonal patterns of mean lipid content (%) values in the flesh of small (LTǩ110 mm), medium (111ǩLTǩ180 mm) and large (LT>181 mm) length categories of male and female four-spotted megrim in the west Aegean Sea. Vertical bars denote standard errors of the means.
Figure 4 in Effects of sexual maturity and feeding on condition of a deep-sea flatfish, Lepidorhombus boscii, in north-eastern Mediterranean waters
Figure 4. Frequency of occurrence of the various maturity stages in male and female gonads of four-spotted megrim collected seasonally in the west Aegean Sea.
Figure 6 in Effects of sexual maturity and feeding on condition of a deep-sea flatfish, Lepidorhombus boscii, in north-eastern Mediterranean waters
Figure 6. Seasonal patterns of mean hepatosomatic factor (HSI) values for small (LTǩ110 mm), medium (111ǩLTǩ180 mm) and large (LT>181 mm) length categories of male and female four-spotted megrim in the west Aegean Sea. Vertical bars denote standard errors of the means.
Feeding Maturity in Preterm Infants
ClinicalTrials.gov study NCT07273266. IPD Sharing: NO. Countries: 1. Publications: 5.
Feeding Tolerance and Gut Maturation of Infants Consuming a Formula Rich in Glycoprotein
ClinicalTrials.gov study NCT04880083. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Fig. 2 in Feeding behavior of Diaphorina citri (Hemiptera: Liviidae) and its acquisition of 'Candidatus Liberibacter asiaticus', on huanglongbing-infected Citrus reticulata leaves of several maturity stages
Fig. 2. Visual representation of EPG waveforms E1 (phloem salivation), E2 (phloem ingestion) and G (xylem ingestion) produced by adult Diaphorina citri feeding on HLB-infected Citrus sunki leaves.
Swallowing Sound in Preterm Infant Evaluation of Feeding Maturation
ClinicalTrials.gov study NCT01944956. IPD Sharing: Not stated. Countries: 0. Publications: 1.
Figure 1 in Effects of sexual maturity and feeding on condition of a deep-sea flatfish, Lepidorhombus boscii, in north-eastern Mediterranean waters
Figure 1. Location of sampling stations.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.