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114 results for “Body Length”
Fig. 1 in The Relationship of Body Length to Fresh Weight Varies Across Three Buprestid Genera (Coleoptera: Buprestidae)
Fig. 1. Individual linear regressions of the relationship of body length and fresh weight of three genera of Buprestidae brought to the nest by Cerceris fumipennis in North Carolina.
dataset for paper entitled "Effect of Moringa Oleifera Leaf Extract On Body Length, Malondialadehyd and Interleukin-6 Levels in Zebrafish Larvae (Danio Rerio) Induced Stunting Model with Rotenone"
<p>The dataset consist of:</p> <p>1. Appendices of tools and material used for laboratory research</p> <p>2. Certificate of ethical test </p> <p>3. Data of moringa oleifera controls</p> <p>4. Data of zebrafish growth </p>
Telomere Length in Human Polar Body and Telomere Length in Cumulus Cells: A Clinical Validation Study
ClinicalTrials.gov study NCT04577560. IPD Sharing: YES. Countries: 1. Publications: 11.
Data from: Length, body depth, and gape relationships and inference on piscivory among North American centrarchids
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Data from: On the comparative biology of mammalian telomeres: telomere length co-evolves with body mass, lifespan and cancer risk
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Data from: Genetic and maternal effects on tail spine and body length in the invasive spiny water flea (Bythotrephes longimanus)
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Data on Tree Swallow (Tachycineta bicolor) body mass, wing, and headbill length
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Data for: Warming temperatures limit the maximum body length of teleost fishes across a latitudinal gradient in Norwegian waters
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Supplementary material 2 from: Hofmann MM, Fleischmann A, Renner SS (2020) Foraging distances in six species of solitary bees with body lengths of 6 to 15 mm, inferred from individual tagging, suggest 150 m-rule-of-thumb for flower strip distances. Journal of Hymenoptera Research 77: 105-117. https://doi.org/10.3897/jhr.77.51182
Table S1
Figure 4 from: Hofmann MM, Fleischmann A, Renner SS (2020) Foraging distances in six species of solitary bees with body lengths of 6 to 15 mm, inferred from individual tagging, suggest 150 m-rule-of-thumb for flower strip distances. Journal of Hymenoptera Research 77: 105-117. https://doi.org/10.3897/jhr.77.51182
Figure 4 Mean flight distances (with standard deviations) calculated from the 450 bee re-sightings shown in Suppl. material 2: Table S1, with year of observation given for Osmia cornuta, studied in both 2017 and 2018. All remaining data are from 2017. Species body sizes are from Amiet et al. (2004) and Scheuchl (2006). For the smaller species Chelostoma florisomne, C. rapunculi, and Heriades truncorum, which were colour-tagged rather than number-tagged, we cannot exclude repeated observations of the same individual.
Figure 3 from: Hofmann MM, Fleischmann A, Renner SS (2020) Foraging distances in six species of solitary bees with body lengths of 6 to 15 mm, inferred from individual tagging, suggest 150 m-rule-of-thumb for flower strip distances. Journal of Hymenoptera Research 77: 105-117. https://doi.org/10.3897/jhr.77.51182
Figure 3 Marking of an Osmia cornuta male (photos: J. Kirndorfer) a application of the glue and b, c attaching of the apiarists' tag d a labeled male ready to take off.
Figure 2 from: Hofmann MM, Fleischmann A, Renner SS (2020) Foraging distances in six species of solitary bees with body lengths of 6 to 15 mm, inferred from individual tagging, suggest 150 m-rule-of-thumb for flower strip distances. Journal of Hymenoptera Research 77: 105-117. https://doi.org/10.3897/jhr.77.51182
Figure 2 Marking of an Osmia cornuta female (photos: J. Kirndorfer). a, b A female caught with an insect net is transferred to the queen-marking tube and c, d pushed with the plunger to immobilize it (e, f a stylus is used to put glue on the mesonotum g, h the numbered colour plate is attached and i the bee released.
Figure 1 from: Hofmann MM, Fleischmann A, Renner SS (2020) Foraging distances in six species of solitary bees with body lengths of 6 to 15 mm, inferred from individual tagging, suggest 150 m-rule-of-thumb for flower strip distances. Journal of Hymenoptera Research 77: 105-117. https://doi.org/10.3897/jhr.77.51182
Figure 1 Marked individuals of AChelostoma florisomneBC. rapunculiCHeriades truncorumDHoplitis aduncaEOsmia bicornis, and FOsmia cornuta.
Supplementary material 1 from: Hofmann MM, Fleischmann A, Renner SS (2020) Foraging distances in six species of solitary bees with body lengths of 6 to 15 mm, inferred from individual tagging, suggest 150 m-rule-of-thumb for flower strip distances. Journal of Hymenoptera Research 77: 105-117. https://doi.org/10.3897/jhr.77.51182
Figure S1. Map showing the garden lay-out and location of the nest boxes at with bees were tagged
Data from: Body length of bony fishes was not a selective factor during the biggest mass extinction of all time
The Permo-Triassic mass extinction devastated life on land and in the sea, but it is not clear why some species survived and others went extinct. One explanation is that lineage loss during mass extinctions is a random process in which luck determines which species survive. Alternatively, a phylogenetic signal in extinction may indicate a selection process operating on phenotypic traits. Large body size has often emerged as an extinction risk factor in studies of modern extinction risk, but this is not so commonly the case for mass extinctions in deep time. Here, we explore the evolution of non-teleostean Actinopterygii (bony fishes) from the Devonian to the present day, and we concentrate on the Permo-Triassic mass extinction. We apply a variety of time-scaling metrics to date the phylogeny, and show that diversity peaked in the latest Permian and declined severely during the Early Triassic. In line with previous evidence, we find the phylogenetic signal of extinction increases across the mass extinction boundary: extinction of species in the earliest Triassic is more clustered across phylogeny compared to the more randomly distributed extinction signal in the late Permian. However, body length plays no role in differential survival or extinction of taxa across the boundary. In the case of fishes, size did not determine which species survived and which went extinct, but phylogenetic signal indicates that the mass extinction was not a random field of bullets.
Data from: Functional traits in red flour beetles: the dispersal phenotype is associated with leg length but not body size nor metabolic rate
Individuals vary in their ability to disperse. Much of this variation can be described by covarying phenotypic traits that are related to dispersal (constituting the 'dispersal phenotype' or 'dispersal syndrome'), but the nature of the associations among these traits is not well understood. Unravelling the associations among traits that potentially constitute the dispersal phenotype provides a foundation for understanding evolutionary trade-offs due to variation in dispersal. Here, we tested five predictions pertaining to the relationships among physiological, morphological and movement traits that are associated with dispersal, using a species with a long history as a laboratory model for studying ecological phenomena, red flour beetles (Tribolium castaneum). We identified a dominant axis of movement ability that describes variation in dispersal-related movement traits. Individuals that scored positively on this axis moved at higher speed, travelled longer distances, had lower movement intermittency and dispersed quicker to a specified area. Relative leg length, but not body size nor routine metabolic rate related positively with movement ability, indicating a likely mechanistic relationship between increased stride length and movement ability. Our data suggest that the dispersal phenotype may be more strongly linked to morphological traits than physiological ones. We demonstrate that associations among many functional traits do not necessarily conform to a priori expectations, and predict that the substantial intraspecific variation in trait values may be important for selection. Movement is a complex behavioural trait, but it has a mechanistic basis in locomotor morphology that warrants further exploration.
FIGURE 3. Phobaeticus chani female holotype, body length 357 in The types of Phasmida in the Natural History Museum, London, UK
FIGURE 3. Phobaeticus chani female holotype, body length 357 mm.
FIGURE 10 in Body length estimation of Neogene macrophagous lamniform sharks (Carcharodon and Otodus) derived from associated fossil dentitions
FIGURE 10. Re-calculation of Otodus megalodon body lengths from Pimiento et al. (2010). (A) Re-calculation using the correct equations from Shimada (2002a). (B) Re-calculation using the SCW direct proportions method, showing results based on CH-31-46P and UF- VP-311000 as analogs separately.
FIGURE 11 in Body length estimation of Neogene macrophagous lamniform sharks (Carcharodon and Otodus) derived from associated fossil dentitions
FIGURE 11. Maximum body length estimation of Otodus megalodon. (A) Widest known tooth of O. megalodon (GHC 6), lingual view. The tooth enamel has been repaired inside the red polygon. Scale bar equals 5 cm. (B) Body length calculation for specimen GHC 6, using the associated dentition UF-VP-311000 as an analog and assuming the tooth represents position L1. SCWc = summed crown width corrected and TL = total body length. (C) Illustration depicting the mathematical equation used to solve for body length. Otodus megalodon artwork by Tim Scheirer, used with permission from the Calvert Marine Museum.
FIGURE 7 in Body length estimation of Neogene macrophagous lamniform sharks (Carcharodon and Otodus) derived from associated fossil dentitions
FIGURE 7. Comparison of body length estimates based on SCW direct proportions and Shimada (2002a) CH linear regression. (A–B) Otodus megalodon; (C–D) Otodus chubutensis; and (E–F) Carcharodon spp. (A, C, E) SCW direct proportions. (B, D, F) Shimada (2002a) CH linear regression. U = upper and L = lower.
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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
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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
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