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Fig. 2 in Centipede diversity in patches of different development phases in an unevenly-aged beech forest stand in Slovenia
Fig. 2. Average density estimates of some centipede species from different development phases in an unevenlyaged beech stand at Is˘ka (Slovenia), based on soil samples in 2000.
Fig. 1 in Centipede diversity in patches of different development phases in an unevenly-aged beech forest stand in Slovenia
Fig. 1. Dendrogram of similarities among centipede community samples from different forest development phases, sampled in three different periods in 2000 (distances calculated as (1-percentage similarity)).
Data file for Augoyard et al.'s article, "Evaluation of age, sex, and ancestry-related variation in cortical bone and dentine volumes in modern humans, and a preliminary assessment of cortical bone-dentine covariation in later Homo"
<p>The following dataset is related to Augoyard et al.'s article: <em>Evaluation of age, sex, and ancestry-related variation in cortical bone and dentine volumes in modern humans, and a preliminary assessment of cortical bone-dentine covariation in later Homo</em>, submitted in september 2022 to the <em>Journal of Archaeological Sciences</em>.</p>
The Absolute Age of M92
<p>10000 sets of isochrones for M92</p>
FIG. 4 in Multi-aged forest fragments in Atlantic France that are surrounded by meadows retain a richer epiphyte lichen flora
FIG. 4. — The significant effect of canopy density on lichen abundance according to the summary of the GLMMs. The GLMM results are presented for the exterior forest at the tree level within the FFs surrounded by meadows, taking into account the larger tree category (details as in Fig. 2).
Figure 1 in Geographical, climatic and biological constraints on age at sexual maturity in amphibians
Figure 1. Geographical locations of the 123 species of amphibians analysed.
Radiocarbon ages of 6 ancient holm oaks growing in Montecristo Island, Italy
<p>Here we present radiocarbon dates of 6 large and ancient holm oak (Quercus ilex L.) trees collected in Montecristo Island (Tuscany, Italy), reported in the paper “Rediscovering Montecristo’s treasure: the island’s holm oaks reveal exceptional longevity” published in Ecology in 2023. The knowledge of the potential maximum lifespans of trees is a key trait for understanding ecosystem functioning and dynamics. However, old trees present often rotten and hollow trunks; moreover, in Mediterranean environment, false and missing rings can further complicate tree-ring studies. Radiocarbon dating is an interesting solution to overcome these problems. Rotten wood samples were collected from the inner and lowest part of each trunk as close as possible to the hypothesized root “collar” and pith. All the sampled wood fragments showed a moderate tree-ring curvature, but we were not able to calculate a reliable estimate of pith-offset (i.e. of the number of missing rings between the innermost annual increment samples and the pith). However, because of the pith offset and the vertical sampling distance from the collar (up to 1 m), radiocarbon dates may have underestimated tree age by a few decades. Radiocarbon dating was carried out by AMS (Accelerator Mass Spectrometry) at CEDAD, the “Centre of Applied Physics, Dating and Diagnostics”, University of Salento, Lecce, Italy. The difference between the calibrated radiocarbon ages and the year 2022 CE was used to calculate the age of each tree. The calculated age range is between 444±90 (probability 92.3%) calendar years for the youngest sampled tree and 761±42 (probability 91.7%) calendar years for the oldest one.</p>
Circulating exosomes decrease in size and increase in number between birth and age 7: relations to fetal growth and liver fat
<p>Circulating exosomes</p>
LENS and NoPin (NP) ensemble means for apparent oxygen utilization (AOU), anthropogenic and preindustrial carbon, pCFC-12, and ideal age from Olivarez et al. (2023)
<p>Manuscript title: <strong>"How does the Pinatubo eruption influence our understanding of long-term changes in ocean biogeochemistry?"</strong></p> <p>Authors: Holly C. Olivarez<sup>1,2</sup>, Nicole S. Lovenduski<sup>2,3</sup>, Yassir A. Eddebbar<sup>4</sup>, Amanda R. Fay<sup>5</sup>, Galen A. McKinley<sup>5</sup>, Michael N. Levy<sup>6</sup>, and Matthew C. Long<sup>6</sup></p> <p>Affiliations:<br> <sup>1</sup>Department of Environmental Studies, University of Colorado, Boulder, CO, USA <br> <sup>2</sup>Institute of Arctic and Alpine Research, University of Colorado, Boulder, CO, USA<br> <sup>3</sup>Department of Atmospheric and Oceanic Sciences, University of Colorado, Boulder, CO, USA <br> <sup>4</sup>Scripps Institution of Oceanography, University of California San Diego, La Jolla, CA, USA <br> <sup>5</sup>Columbia University and Lamont-Doherty Earth Observatory, Palisades, NY, USA <br> <sup>6</sup>Climate and Global Dynamics Laboratory, National Center for Atmospheric Research, Boulder, Colorado, USA</p> <p>LENS and No Pinatubo (NoPin in manuscript, NP in file names) CESM ensemble means for apparent oxygen utilization (AOU), anthropogenic and preindustrial carbon, <em>p</em>CFC-12, and ideal age along GO-SHIP transects akin to <a href="https://cchdo.ucsd.edu/data/4925/33RO20130803do.pdf">A16N</a>, <a href="https://cchdo.ucsd.edu/data/9276/33RO20131223do.pdf">A16S</a>, <a href="https://cchdo.ucsd.edu/data/14283/33RO20150525_do.pdf">P16N</a>, <a href="https://cchdo.ucsd.edu/cruise/320620140320#note_334284">P16S</a>, <a href="https://cchdo.ucsd.edu/cruise/09AR20060102">SO4I</a>, <a href="https://cchdo.ucsd.edu/cruise/320620180309">SO4P</a>.</p> <p>The CESM source code is freely available at <a href="http://www2.cesm.ucar.edu">http://www2.cesm.ucar.edu</a>. The model outputs described in this paper can be accessed at <a href="http://www.earthsystemgrid.org">www.earthsystemgrid.org</a>.</p>
Fig. 2 in Chemical constituents of Antidesma bunius aerial parts and the anti-AGEs activity of selected compounds
Fig. 2. Key HMBC (H→C) and 1H–1H COSY correlations of compounds 1–5, 8, 16, 17, and 20.
Fig. 1 in Chemical constituents of Antidesma bunius aerial parts and the anti-AGEs activity of selected compounds
Fig. 1. (continued).
Fig. 1 in Chemical constituents of Antidesma bunius aerial parts and the anti-AGEs activity of selected compounds
Fig. 1. Chemical structures of isolated compounds from A. bunius aerial parts.
Search strategies for universal vaccination with an enhanced inactivated influenza vaccine in those aged 65 years and older
<p>The dataset includes the complete, reproducible search strategies for all literature databases searched during this project. The search strategies were designed to answer the following research question: </p> <p>What is the cost-effectiveness of universal vaccination with an enhanced inactivated influenza vaccine in those aged 65 years and older?</p> <p> </p> <p> </p>
Petrology, Age, and Rift Origin of Ultramafic Lamprophyres (Aillikites) at Mount Webb, a New Alkaline Province in Central Australia
<p>APPENDIX_A: LA-ICP-MS and EPMA analyses for pyrope garnet and Cr diopside used in study.</p>
Data from: Forest age is a primary trait filter for saproxylic beetles in the southeastern United States
<p>Data from: Forest age is a primary trait filter for saproxylic beetles in the southeastern United States</p> <p>Clayton R. Traylor, Michael D. Ulyshen, Joseph V. McHugh, Ryan C. Burner</p> <p>Forest Ecology and Management 553: 121545. </p> <p><a title="Persistent link using digital object identifier" href="https://doi.org/10.1016/j.foreco.2023.121545" target="_blank" rel="noreferrer noopener"><span>https://doi.org/10.1016/j.foreco.2023.121545</span></a> </p> <p> </p> <p>Corresponding author: Clayton R. Traylor, <a href="mailto:clayton.r.traylor@gmail.com">clayton.r.traylor@gmail.com</a></p> <p> </p> <p> </p> <p><strong>Abstract</strong></p> <p>Many forests throughout the world consist of regenerating mature stands. Although these forests differ in many respects from old-growth (with a history of minimal human disturbance), they typically develop similar structural attributes over time. As a result, older mature forests may be of particular conservation value if they contain resources and microhabitats benefitting saproxylic (deadwood dependent) species. Species' response to forest age may be driven by traits that relate to ecological functions or habitat preferences, such that species with less compatible traits for a local forest environment are "filtered" out. Thus, forest age may influence species' distributions and the trait composition of assembled communities. </p> <p>The Piedmont region of the southeastern United States has experienced widespread forest regrowth over the past century due to agricultural abandonment. Today's landscapes are largely characterized by mature forests that are becoming increasingly fragmented by suburbanization. Here, we assessed the filtering effects of forest age, landscape forest cover (LFC), and deadwood volume on saproxylic beetles in northeastern Georgia. Using historic aerial imagery to distinguish forest age (young = regrown after 1938; old = mature in 1938), we sampled beetles in mature forests of both age classes occurring along an LFC gradient. We measured five traits with hypothesized functional roles (body length, body width, body roundness, antenna length, eye length) for the 472 species captured. Using a joint species distribution model (JSDM), we tested trait-niche relationships (i.e., how traits influence species' responses) and estimated community trait composition (mean and dispersion of trait values) along gradients of environmental filters.</p> <p>We found that forest age is a filter for several traits (six supported relationships with >95% posterior probability), but LFC and deadwood volume were less strongly related to fewer traits. Most notably, large species (typically having lower population sizes and requiring stable larval habitat) were filtered from young mature forests and low LFC. Thus, old mature forests with high LFC showed higher mean and dispersion of beetle body length. Sensory traits also showed responses, likely reflecting adult life under bark (eye length) or ability to detect resources or mates (antenna length). Body width and roundness showed inconsistent responses with regard to indicated functional roles. Our results show that forest age is a strong filter on saproxylic beetle communities in the southeastern United States. Old mature forests, despite their scarcity in the region, are important for species requiring habitat stability and for maintaining communities with diverse trait composition.</p> <p> </p>
Age-related differences in Bilateral Synergistic Coordination of the Upper Extremity
<p>Data collected from two groups of subjects with mean ages of 23 and 55, performing three tasks of the upper extremity requiring bilateral coordination.</p>
Figure 3. – Mean condition factor K in Reproduction, age and growth of Tilapia zillii (Cichlidae) in Oued Righ wetland (southeast Algeria)
Figure 3. – Mean condition factor K according to sex and season of T. zillii. Male: ε = 4.92; α = 5 %; female: ε = 4.5; α = 5 %).
Figure 2 in Reproduction, age and growth of Tilapia zillii (Cichlidae) in Oued Righ wetland (southeast Algeria)
Figure 2. – Mean gonadosomatic index (GSI) and mean hepatosomatic index (HSI) in T. zillii males and females of Oued Righ wetland, from October 2011 to September 2012. Vertical bars indicate SEM.
Figure 3 in Age and growth of Conger conger (Congridae) from the north coast of Tunisia
Figure 3. – Views of transverse section of an otolith of Conger conger observed with reflected light (×20). Otolith from a 995 mmtotal length specimen (five annuli present).
Figure 4 in Age and growth of Conger conger (Congridae) from the north coast of Tunisia
Figure 4. – Views of transverse section of an otolith observed with reflected light (×20). Otolith from a 238 mm-total length Conger conger (only one annulus present).
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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.