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67 results for “adult size”
Data from: Social brain volume is associated with in-degree social network size among older adults
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Trans-generational effect of protein restricted diet on adult body and wing size of Drosophila melanogaster
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Host and oak species impact clutch and adult size of Oobius rudnevi, the only known egg parasitoid of Cerambyx beetles
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Data from: Relationship between effective population size, inbreeding, and adult fitness-related traits in a steelhead (Oncorhynchus mykiss) population released in the wild
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Data from: Density-dependent offspring interactions do not explain macroevolutionary scaling of adult size and offspring size
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Data from: Spatiotemporal relationship between adult census size and genetic population size across a wide population size gradient
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Evolution of reduced minimum critical size as a response to selection for rapid pre-adult development in Drosophila melanogaster.
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Comparison of adult census size and effective population size support the need for continued protection of two Solomon Island endemics
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Shape coordinates and centroid size for adults and ontogenetic series analyzed in predictable complexity of evolutionary allometry
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Structural size measurements and isotopic signatures of foraging among adult male and female Adélie penguins (Pygoscelis adeliae) nesting along the Palmer Archipelago near Palmer Station, 2007-2009
Sexual segregation in vertebrate foraging niche is often associated with sexual size dimorphism (SSD), i.e., ecological sexual dimorphism. We examined ecological sexual dimorphism among sympatric nesting Pygoscelis penguins near Palmer Station, Antarctica, asking whether environmental variability in the form of winter sea ice is associated with differences in male and female pre-breeding foraging niche. Each season, study nests, where pairs of adults were present, were individually marked and chosen before the onset of egg-laying, and consistently monitored. When study nests were found at the one-egg stage, both adults were captured to obtain blood samples used for molecular sexing and stable isotope analyses, and measurements of structural size and body mass. At the time of capture, each adult penguin was quickly blood sampled (~1 ml) from the brachial vein. After handling, individuals at study nests were further monitored to ensure the pair reached clutch completion, i.e., two eggs. Molecular analyses were conducted at Simon Fraser University following standard PCR protocols, and stable isotope analyses were conducted at the Stable Isotope Facility at the University of California, Davis using an elemental analyzer interfaced with an isotope ratio mass spectrometer
Structural size measurements and isotopic signatures of foraging among adult male and female gentoo penguins (Pygoscelis papua) nesting along the Palmer Archipelago near Palmer Station, 2007-2009
Sexual segregation in vertebrate foraging niche is often associated with sexual size dimorphism (SSD), i.e., ecological sexual dimorphism. We examined ecological sexual dimorphism among sympatric nesting Pygoscelis penguins near Palmer Station, Antarctica, asking whether environmental variability in the form of winter sea ice is associated with differences in male and female pre-breeding foraging niche. Each season, study nests, where pairs of adults were present, were individually marked and chosen before the onset of egg-laying, and consistently monitored. When study nests were found at the one-egg stage, both adults were captured to obtain blood samples used for molecular sexing and stable isotope analyses, and measurements of structural size and body mass. At the time of capture, each adult penguin was quickly blood sampled (~1 ml) from the brachial vein. After handling, individuals at study nests were further monitored to ensure the pair reached clutch completion, i.e., two eggs. Molecular analyses were conducted at Simon Fraser University following standard PCR protocols, and stable isotope analyses were conducted at the Stable Isotope Facility at the University of California, Davis using an elemental analyzer interfaced with an isotope ratio mass spectrometer
Structural size measurements and isotopic signatures of foraging among adult male and female Chinstrap penguins (Pygoscelis antarcticus) nesting along the Palmer Archipelago near Palmer Station, 2007-2009
Sexual segregation in vertebrate foraging niche is often associated with sexual size dimorphism (SSD), i.e., ecological sexual dimorphism. We examined ecological sexual dimorphism among sympatric nesting Pygoscelis penguins near Palmer Station, Antarctica, asking whether environmental variability in the form of winter sea ice is associated with differences in male and female pre-breeding foraging niche. Each season, study nests, where pairs of adults were present, were individually marked and chosen before the onset of egg-laying, and consistently monitored. When study nests were found at the one-egg stage, both adults were captured to obtain blood samples used for molecular sexing and stable isotope analyses, and measurements of structural size and body mass. At the time of capture, each adult penguin was quickly blood sampled (~1 ml) from the brachial vein. After handling, individuals at study nests were further monitored to ensure the pair reached clutch completion, i.e., two eggs. Molecular analyses were conducted at Simon Fraser University following standard PCR protocols, and stable isotope analyses were conducted at the Stable Isotope Facility at the University of California, Davis using an elemental analyzer interfaced with an isotope ratio mass spectrometer
METHODS. Bovine ilia were used in the simulations because their histological structure (a fibrolamellar cortex overlying cancellous bone26) was found to match that of the Triceratops ilium. Bone sections 10 x 50 x 縠 3.0 cm with cortices ranging from 0.5 to 5.5 mm in depth (the range of initial cortical-thickness estimates based on gross morphology) were mounted on a servohydraulic mechanical loading frame (MTS Bionix, Minneapolis) and penetrated with an aluminium-bronze T. rex tooth replica. The replica was cast from an actual adult T. rex maxillary tooth, after casts made from some ofthe deeper bite marks revealed the size and shape of the teeth that had impacted the pelvis8 • The replica was penetrated into the ilia sections at 1 mm s-1 to a depth of 11.5 mm, equivalent to the maximum depth of the deepest ilium bite mark8 • Forces were measured with an MTS 25 N strain-gauge-based axial load cell accurate to 0.2%. The forces increased with increasing penetration depth even after the cortical layer had been perforated and the underlying cancellous bone was being crushed. The increase in force with penetration depth is attributed to a greater cortical surface area coming into contact with the semi-conical penetrator tooth as it descended through the ilia. in Bite-force estimation for Tyrannosaurus rex from tooth-marked bones
METHODS. Bovine ilia were used in the simulations because their histological structure (a fibrolamellar cortex overlying cancellous bone26) was found to match that of the Triceratops ilium. Bone sections 10 x 50 x 縠 3.0 cm with cortices ranging from 0.5 to 5.5 mm in depth (the range of initial cortical-thickness estimates based on gross morphology) were mounted on a servohydraulic mechanical loading frame (MTS Bionix, Minneapolis) and penetrated with an aluminium-bronze T. rex tooth replica. The replica was cast from an actual adult T. rex maxillary tooth, after casts made from some ofthe deeper bite marks revealed the size and shape of the teeth that had impacted the pelvis8 • The replica was penetrated into the ilia sections at 1 mm s-1 to a depth of 11.5 mm, equivalent to the maximum depth of the deepest ilium bite mark8 • Forces were measured with an MTS 25 N strain-gauge-based axial load cell accurate to 0.2%. The forces increased with increasing penetration depth even after the cortical layer had been perforated and the underlying cancellous bone was being crushed. The increase in force with penetration depth is attributed to a greater cortical surface area coming into contact with the semi-conical penetrator tooth as it descended through the ilia.
Data from: A phylogenetic analysis of egg size, clutch size, spawning mode, adult body size, and latitude in reef fishes
Theoretical treatments of egg size in fishes suggest that constraints on reproductive output should create trade-offs between the size and number of eggs produced per spawn. For marine reef fishes, the observation of distinct reproductive care strategies (demersal guarding, egg scattering, and pelagic spawning) has additionally prompted speculation that these strategies reflect alternative fitness optima with selection on egg size differing by reproductive mode and perhaps latitude. Here, we aggregate data from 278 reef fish species and test whether clutch size, reproductive care, adult body size, and latitudinal bands (i.e., tropical, subtropical, and temperate) predict egg size, using a statistically unified framework that accounts for phylogenetic correlations among traits. We find no inverse relationship between species egg size and clutch size, but rather that egg size differs by reproductive mode (mean volume for demersal eggs = 1.22 mm3, scattered eggs = 0.18 mm3, pelagic eggs = 0.52 mm3) and that clutch size is strongly correlated with adult body size. Larger eggs were found in temperate species compared with tropical species in both demersal guarders and pelagic spawners, but this difference was not strong when accounting for phylogenetic correlations, suggesting that differences in species composition underlies regional differences in egg size. In summary, demersal guarders are generally small fishes with small clutch sizes that produce large eggs. Pelagic spawners and egg scatterers are variable in adult and clutch size. Although pelagic spawned eggs are variable in size, those of scatterers are consistently small.
Data from: Does phenotypic plasticity for adult size versus food level in Drosophila melanogaster evolve in response to adaptation to different rearing densities?
Recent studies using inbred lines of Drosophila have suggested that there is extensive genetic variability for phenotypic plasticity of body size versus food level. If true, we expect that the outcome of evolution at very different food levels should yield genotypes whose adult sizes show different patterns of phenotypic plasticity. We have tested this prediction with six independent populations of Drosophila melanogaster kept at extreme (low vs. high) densities for 125 generations. We found that the phenotypic plasticity of body size versus food level is not affected by selection or the presence of competitors of a different genotype. However, we document increasing among population variation in phenotypic plasticity due to random genetic drift. Several reasons are explored to explain these results including the possibility that the use of highly inbred lines to make inferences about the evolution of genetically variable populations may be misleading.
Morphometrics of taxa in the genus Sphenopsis, recorded from adult male (n = 21) and female (n = 15) study skins in the Academy of Natural Sciences of Drexel University, Philadelphia (ANSP) and Delaware Museum of Nature & Science, Greenville (DMNH) collections. Sample sizes and means (± SD) are given for each taxon, within each sex class (female, male), for the following variables: (WG) wing length, (TR) tarsometatarsus length, (TL) tail length, (BL) bill length, and (BW) bill width. All measurements in mm. in Taxonomic status of the Western Hemispingus Sphenopsis ochracea (Thraupidae) and a review of species limits in the genus Sphenopsis P. L. Sclater, 1861
Morphometrics of taxa in the genus Sphenopsis, recorded from adult male (n = 21) and female (n = 15) study skins in the Academy of Natural Sciences of Drexel University, Philadelphia (ANSP) and Delaware Museum of Nature & Science, Greenville (DMNH) collections. Sample sizes and means (± SD) are given for each taxon, within each sex class (female, male), for the following variables: (WG) wing length, (TR) tarsometatarsus length, (TL) tail length, (BL) bill length, and (BW) bill width. All measurements in mm.
Investigation of Trunk Muscle Size and Function in Older Adults With Chronic Low Back Pain
ClinicalTrials.gov study NCT01221233. IPD Sharing: NO. Countries: 1. Publications: 0.
Data from: A phylogenetic analysis of egg size, clutch size, spawning mode, adult body size, and latitude in reef fishes
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Data from: Does phenotypic plasticity for adult size versus food level in Drosophila melanogaster evolve in response to adaptation to different rearing densities?
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Ependyma-expressed CCN1 restricts the size of the neural stem cell pool in the adult ventricular-subventricular zone
GEO Series GSE137852. Mus musculus. 6 samples. Type: Expression profiling by high throughput sequencing.
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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)
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.