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Anatomical wood traits of tree species in old-growth and selectively logged forest
<b>Description: </b><p>Traits matrix of wood anatomical characteristics for tree species in selectively logged forest at SAFE and in old-growth forest in Danum Valley and Maliau Basin. Sampled during the BALI project traits campaign</p><p><b>Project: </b>This dataset was collected as part of the following SAFE research project: <a href="https://www.safeproject.net/projects/project_view/55"><b>Biodiversity and land-use impacts on tropical ecosystem function (BALI): Quantifying functional trait distributions across the disturbance gradient</b></a></p><p><b>Funding: </b>These data were collected as part of research funded by: </p><ul><li>NERC (Standard grant, NE/K016253/1)</li></ul><p>This dataset is released under the CC-BY 4.0 licence, requiring that you cite the dataset in any outputs, but has the additional condition that you acknowledge the contribution of these funders in any outputs.</p><p></p><p><b>Permits: </b>These data were collected under permit from the following authorities:</p><ul><li>Sabah Biodiversity Centre (Research licence JKM/MBS.1000-2.2(385))</li></ul><p></p><p><b>XML metadata: </b>GEMINI compliant metadata for this dataset is available <a href="https://www.safeproject.net/datasets/xml_metadata?id=5513918">here</a></p><p><b>Files: </b>This consists of 1 file: Both_wood_anatomical_traits_complete_dataset.xlsx</p><p><b>Both_wood_anatomical_traits_complete_dataset.xlsx</b></p><p>This file contains dataset metadata and 1 data tables:</p><ol><li><p><b>Wood_anatomical_traits</b> (described in worksheet Wood_anatomical_traits)</p><p>Description: Traits matrix of wood anatomical characteristics for tree species in selectively logged forest at SAFE and in old-growth forest in Danum Valley and Maliau Basin. Sampled during the BALI project traits campaign</p><p>Number of fields: 18</p><p>Number of data rows: 596</p><p>Fields: </p><ul><li><b>location</b>: Location (Field type: location)</li><li><b>forest_type</b>: Forest type: OG: old-growth plots, Maliau and Danum; SL: selectively logged plots at SAFE (Field type: categorical)</li><li><b>forestplots_name</b>: Plot name coherent with forestplots database (Field type: id)</li><li><b>plot_name_trait_campaign</b>: Plot name used during the BALI trait campaign (Field type: id)</li><li><b>sample_code</b>: Sample code referencing: plot-'T'(ree) ID-branch type (Field type: id)</li><li><b>branch_type</b>: Binary classification of branch sampled depending on their position in the tree crown. BS: sun branch; BSH: shade branch (Field type: id)</li><li><b>sampling_date</b>: Date of sampling (Field type: date)</li><li><b>tree_id</b>: Reference for tree tag label (Field type: id)</li><li><b>species</b>: Tree species (Field type: taxa)</li><li><b>Wedge.area.micron2</b>: Area of wedge from microtome slice used for analysis. (Field type: numeric trait)</li><li><b>No.vessel.wedge</b>: Count of vessels in the respective wedge area. (Field type: numeric trait)</li><li><b>Vessel.diameter.micron</b>: Mean vessel diameter. Vessel diameter is determined as the mean of the maximum and minimum (lumen) diameters. (Field type: numeric trait)</li><li><b>Median.vessel.diameter.micron</b>: The middle value of the vessel diameter data set. (Field type: numeric trait)</li><li><b>Hydraulically.weighted.diameter.micron</b>: Hydraulically weighted mean diameter. Calculated as (∑ diameter^5) / (∑ diameter^4). (Field type: numeric trait)</li><li><b>Vessel.area.micron2</b>: Mean vessel area. Vessel area is determined by the average cross-sectional area of all vessel lumens (excluding vessel walls) in the wedge-shaped transect of the branch wood cross-section. (Field type: numeric trait)</li><li><b>Median.vessel.area.micron2</b>: The middle value of the vessel area data set. (Field type: numeric trait)</li><li><b>Vessel.lumen.tot.area</b>: Total area of the vessel lumens in the wedge-shaped transect of the branch wood cross-section. (Field type: numeric trait)</li><li><b>vessel.lumen.f.wedge</b>: Vessel lumen fraction. From the vessel areas and transect areas, vessel lumen fraction is calculated as the fraction of transect area filled by vessel lumens. (Field type: numeric trait)</li></ul></li></ol><p><b>Date range: </b>2014-05-01 to 2018-09-01</p><p><b>Latitudinal extent: </b>4.5000 to 5.0700</p><p><b>Longitudinal extent: </b>116.7500 to 117.8200</p><p><b>Taxonomic coverage: </b><br> All taxon names are validated against the GBIF backbone taxonomy. If a dataset uses a synonym, the accepted usage is shown followed by the dataset usage in brackets. Taxa that cannot be validated, including new species and other unknown taxa, morphospecies, functional groups and taxonomic levels not used in the GBIF backbone are shown in square brackets.</p><div> -  Plantae <br> -  -  Tracheophyta <br> -  -  -  Magnoliopsida <br> -  -  -  -  Malpighiales <br> -  -  -  -  -  Chrysobalanaceae <br> -  -  -  -  -  -  <i>Licania</i> <br> -  -  -  -  -  -  -  <i>Licania splendens</i> <br> -  -  -  -  -  Hypericaceae <br> -  -  -  -  -  -  <i>Cratoxylum</i> <br> -  -  -  -  -  Irvingiaceae <br> -  -  -  -  -  -  <i>Irvingia</i> <br> -  -  -  -  -  -  -  <i>Irvingia malayana</i> <br> -  -  -  -  -  Centroplacaceae <br> -  -  -  -  -  -  <i>Bhesa</i> <br> -  -  -  -  -  -  -  <i>Bhesa indica</i> (as synonym: <i>Bhesa paniculata</i>)<br> -  -  -  -  -  Clusiaceae <br> -  -  -  -  -  -  <i>Garcinia</i> <br> -  -  -  -  -  -  -  <i>Garcinia benthamiana</i> <br> -  -  -  -  -  -  -  <i>Garcinia forbesii</i> <br> -  -  -  -  -  -  -  <i>Garcinia parvifolia</i> <br> -  -  -  -  -  Salicaceae <br> -  -  -  -  -  -  <i>Homalium</i> <br> -  -  -  -  -  -  -  <i>Homalium foetidum</i> <br> -  -  -  -  -  Putranjivaceae <br> -  -  -  -  -  -  <i>Drypetes</i> <br> -  -  -  -  -  -  -  <i>Drypetes longifolia</i> <br> -  -  -  -  -  Achariaceae <br> -  -  -  -  -  -  <i>Hydnocarpus</i> <br> -  -  -  -  -  -  <i>Ryparosa</i> <br> -  -  -  -  -  -  -  <i>Ryparosa acuminata</i> <br> -  -  -  -  -  Euphorbiaceae <br> -  -  -  -  -  -  <i>Spathiostemon</i> <br> -  -  -  -  -  -  <i>Hancea</i> <br> -  -  -  -  -  -  -  <i>Hancea penangensis</i> (as synonym: <i>Mallotus penangensis</i>)<br> -  -  -  -  -  -  <i>Neoscortechinia</i> <br> -  -  -  -  -  -  -  <i>Neoscortechinia kingii</i> <br> -  -  -  -  -  -  -  <i>Neoscortechinia philippinensis</i> <br> -  -  -  -  -  -  <i>Mallotus</i> <br> -  -  -  -  -  -  -  <i>Mallotus leucodermis</i> <br> -  -  -  -  -  -  -  <i>Mallotus miquelianus</i> <br> -  -  -  -  -  -  -  <i>Mallotus mollissimus</i> <br> -  -  -  -  -  -  -  <i>Mallotus wrayi</i> <br> -  -  -  -  -  -  <i>Ptychopyxis</i> <br> -  -  -  -  -  -  -  <i>Ptychopyxis arborea</i> <br> -  -  -  -  -  -  <i>Macaranga</i> <br> -  -  -  -  -  -  -  <i>Macaranga conifera</i> <br> -  -  -  -  -  -  -  <i>Macaranga gigantea</i> <br> -  -  -  -  -  -  -  <i>Macaranga hypoleuca</i> <br> -  -  -  -  -  -  -  <i>Macaranga pearsonii</i> <br> -  -  -  -  -  -  -  <i>Macaranga winkleri</i> <br> -  -  -  -  -  -  <i>Blumeodendron</i> <br> -  -  -  -  -  -  -  <i>Blumeodendron kurzii</i> <br> -  -  -  -  -  -  -  <i>Blumeodendron tokbrai</i> <br> -  -  -  -  -  Phyllanthaceae <br> -  -  -  -  -  -  <i>Aporosa</i> (as synonym: <i>Aporusa</i>)<br> -  -  -  -  -  -  <i>Cleistanthus</i> <br> -  -  -  -  -  -  -  <i>Cleistanthus hirsutulus</i> <br> -  -  -  -  -  -  -  <i>Cleistanthus hylandii</i> <br> -  -  -  -  -  -  -  <i>Cleistanthus oblongifolius</i> (as synonym: <i>Cleistanthus myrianthus</i>)<br> -  -  -  -  -  -  <i>Glochidion</i> <br> -  -  -  -  -  -  <i>Phyllanthus</i> <br> -  -  -  -  -  -  -  <i>Phyllanthus lutescens</i> (as synonym: <i>Glochidion lutescens</i>)<br> -  -  -  -  -  -  -  <i>Phyllanthus ruber</i> (as synonym: <i>Glochidion rubrum</i>)<br> -  -  -  -  -  -  <i>Baccaurea</i> <br> -  -  -  -  -  -  -  <i>Baccaurea lanceolata</i> <br> -  -  -  -  -  -  -  <i>Baccaurea macrocarpa</i> <br> -  -  -  -  -  -  -  <i>Baccaurea tetrandra</i> <br> -  -  -  -  -  Calophyllaceae <br> -  -  -  -  -  -  <i>Mesua</i> <br> -  -  -  -  -  -  -  <i>Mesua oblongifolia</i> (as synonym: <i>Kayea oblongifolia</i>)<br> -  -  -  -  -  -  -  <i>Mesua macrantha</i> <br> -  -  -  -  -  -  <i>Calophyllum</i> <br> -  -  -  -  -  -  -  <i>Calophyllum soulattri</i> <br> -  -  -  -  Malvales <br> -  -  -  -  -  Malvaceae <br> -  -  -  -  -  -  <i>Heritiera</i> <br> -  -  -  -  -  -  -  <i>Heritiera elata</i> <br> -  -  -  -  -  -  <i>Pterygota</i> <br> -  -  -  -  -  -  -  <i>Pterygota alata</i> <br> -  -  -  -  -  -  <i>Pentace</i> <br> -  -  -  -  -  -  -  <i>Pentace borneensis</i> (as synonym: <i>Pentace laxiflora</i>)<br> -  -  -  -  -  -  <i>Sterculia</i> <br> -  -  -  -  -  -  -  <i>Sterculia stipulata</i> <br> -  -  -  -  -  -  <i>Microcos</i> <br> -  -  -  -  -  -  -  <i>Microcos crassifolia</i> <br> -  -  -  -  -  -  <i>Scaphium</i> <br> -  -  -  -  -  -  -  <i>Scaphium macropodum</i> <br> -  -  -  -  -  -  <i>Boschia</i> <br> -  -  -  -  -  -  -  <i>Boschia grandiflora</i> (as synonym: <i>Durio grandiflorus</i>)<br> -  -  -  -  -  -  <i>Durio</i> <br> -  -  -  -  -  -  -  <i>Durio graveolens</i> <br> -  -  -  -  -  Dipterocarpaceae <br> -  -  -  -  -  -  <i>Shorea</i> <br> -  -  -  -  -  -  -  <i>Shorea almon</i> <br> -  -  -  -  -  -  -  <i>Shorea angustifolia</i> <br> -  -  -  -  -  -  -  <i>Shorea argentifolia</i> <br> -  -  -  -  -  -  -  <i>Shorea beccariana</i> <br> -  -  -  -  -  -  -  <i>Shorea faguetiana</i> <br> -  -  -  -  -  -  -  <i>Shorea falciferoides</i> <br> -  -  -  -  -  -  -  <i>Shorea fallax</i> <br> -  -  -  -  -  -  -  <i>Shorea gibbosa</i> <br> -  -  -  -  -  -  -  <i>Shorea guiso</i> <br> -  -  -  -  -  -  -  <i>Shorea johorensis</i> <br> -  -  -  -  -  -  -  <i>Shorea leprosula</i> <br> -  -  -  -  -  -  -  <i>Shorea leptoderma</i> <br> -  -  -  -  -  -  -  <i>Shorea macrophylla</i> <br> -  -  -  -  -  -  -  <i>Shorea macroptera</i> <br> -  -  -  -  -  -  -  <i>Shorea ovalis</i> <br> -  -  -  -  -  -  -  <i>Shorea ovata</i> <br> -  -  -  -  -  -  -  <i>Shorea parviflora</i> <br> -  -  -  -  -  -  -  <i>Shorea parvifolia</i> <br> -  -  -  -  -  -  -  <i>Shorea parvistipulata</i> <br> -  -  -  -  -  -  -  <i>Shorea pauciflora</i> <br> -  -  -  -  -  -  -  <i>Shorea pinanga</i> <br> -  -  -  -  -  -  -  <i>Shorea superba</i> <br> -  -  -  -  -  -  -  <i>Shorea symingtonii</i> <br> -  -  -  -  -  -  -  <i>Shorea xanthophylla</i> <br> -  -  -  -  -  -  <i>Shorea</i> <br> -  -  -  -  -  -  -  <i>Shorea almon</i> <br> -  -  -  -  -  -  -  <i>Shorea angustifolia</i> <br> -  -  -  -  -  -  -  <i>Shorea argentifolia</i> <br> -  -  -  -  -  -  -  <i>Shorea beccariana</i> <br> -  -  -  -  -  -  -  <i>Shorea faguetiana</i> <br> -  -  -  -  -  -  -  <i>Shorea falciferoides</i> <br> -  -  -  -  -  -  -  <i>Shorea fallax</i> <br> -  -  -  -  -  -  -  <i>Shorea gibbosa</i> <br> -  -  -  -  -  -  -  <i>Shorea guiso</i> <br> -  -  -  -  -  -  -  <i>Shorea johorensis</i> <br> -  -  -  -  -  -  -  <i>Shorea leprosula</i> <br> -  -  -  -  -  -  -  <i>Shorea leptoderma</i> <br> -  -  -  -  -  -  -  <i>Shorea macrophylla</i> <br> -  -  -  -  -  -  -  <i>Shorea macroptera</i> <br> -  -  -  -  -  -  -  <i>Shorea ovalis</i> <br> -  -  -  -  -  -  -  <i>Shorea ovata</i> <br> -  -  -  -  -  -  -  <i>Shorea parviflora</i> <br> -  -  -  -  -  -  -  <i>Shorea parvifolia</i> <br> -  -  -  -  -  -  -  <i>Shorea parvistipulata</i> <br> -  -  -  -  -  -  -  <i>Shorea pauciflora</i> <br> -  -  -  -  -  -  -  <i>Shorea pinanga</i> <br> -  -  -  -  -  -  -  <i>Shorea superba</i> <br> -  -  -  -  -  -  -  <i>Shorea symingtonii</i> <br> -  -  -  -  -  -  -  <i>Shorea xanthophylla</i> <br> -  -  -  -  -  -  <i>Vatica</i> <br> -  -  -  -  -  -  -  <i>Vatica dulitensis</i> <br> -  -  -  -  -  -  -  <i>Vatica odorata</i> <br> -  -  -  -  -  -  <i>Hopea</i> <br> -  -  -  -  -  -  -  <i>Hopea plagata</i> <br> -  -  -  -  -  -  -  <i>Hopea sangal</i> <br> -  -  -  -  -  -  <i>Dipterocarpus</i> <br> -  -  -  -  -  -  -  <i>Dipterocarpus caudiferus</i> <br> -  -  -  -  -  -  <i>Dryobalanops</i> <br> -  -  -  -  -  -  -  <i>Dryobalanops lanceolata</i> <br> -  -  -  -  -  -  <i>Parashorea</i> <br> -  -  -  -  -  -  -  <i>Parashorea malaanonan</i> <br> -  -  -  -  -  -  -  <i>Parashorea smythiesii</i> <br> -  -  -  -  -  -  -  <i>Parashorea warburgii</i> (as synonym: <i>Parashorea tomentella</i>)<br> -  -  -  -  -  Thymelaeaceae <br> -  -  -  -  -  -  <i>Aquilaria</i> <br> -  -  -  -  -  -  -  <i>Aquilaria beccariana</i> <br> -  -  -  -  Celastrales <br> -  -  -  -  -  Celastraceae <br> -  -  -  -  -  -  <i>Lophopetalum</i> <br> -  -  -  -  -  -  -  <i>Lophopetalum beccarianum</i> <br> -  -  -  -  -  -  -  <i>Lophopetalum javanicum</i> <br> -  -  -  -  Santalales <br> -  -  -  -  -  Coulaceae <br> -  -  -  -  -  -  <i>Ochanostachys</i> <br> -  -  -  -  -  -  -  <i>Ochanostachys amentacea</i> <br> -  -  -  -  Fagales <br> -  -  -  -  -  Fagaceae <br> -  -  -  -  -  -  <i>Lithocarpus</i> <br> -  -  -  -  -  -  -  <i>Lithocarpus blumeanus</i> <br> -  -  -  -  -  -  -  <i>Lithocarpus conocarpus</i> <br> -  -  -  -  -  -  -  <i>Lithocarpus echinifer</i> <br> -  -  -  -  -  -  -  <i>Lithocarpus gracilis</i> <br> -  -  -  -  -  -  -  <i>Lithocarpus leptogyne</i> <br> -  -  -  -  -  -  -  <i>Lithocarpus sundaicus</i> <br> -  -  -  -  -  -  <i>Lithocarpus</i> <br> -  -  -  -  -  -  -  <i>Lithocarpus blumeanus</i> <br> -  -  -  -  -  -  -  <i>Lithocarpus conocarpus</i> <br> -  -  -  -  -  -  -  <i>Lithocarpus echinifer</i> <br> -  -  -  -  -  -  -  <i>Lithocarpus gracilis</i> <br> -  -  -  -  -  -  -  <i>Lithocarpus leptogyne</i> <br> -  -  -  -  -  -  -  <i>Lithocarpus sundaicus</i> <br> -  -  -  -  -  -  <i>Quercus</i> <br> -  -  -  -  -  -  -  <i>Quercus argentata</i> <br> -  -  -  -  -  -  -  <i>Quercus lowii</i> <br> -  -  -  -  -  -  -  <i>Quercus merrillii</i> <br> -  -  -  -  -  -  <i>Trigonobalanus</i> <br> -  -  -  -  -  -  -  <i>Trigonobalanus verticillata</i> <br> -  -  -  -  -  -  <i>Castanopsis</i> <br> -  -  -  -  -  -  -  <i>Castanopsis hypophoenicea</i> <br> -  -  -  -  Lamiales <br> -  -  -  -  -  Lamiaceae <br> -  -  -  -  -  -  <i>Callicarpa</i> <br> -  -  -  -  -  -  -  <i>Callicarpa pentandra</i> <br> -  -  -  -  -  Oleaceae <br> -  -  -  -  -  -  <i>Chionanthus</i> <br> -  -  -  -  -  -  -  <i>Chionanthus macrocarpus</i> <br> -  -  -  -  -  -  -  <i>Chionanthus pluriflorus</i> <br> -  -  -  -  Rosales <br> -  -  -  -  -  Urticaceae <br> -  -  -  -  -  -  <i>Dendrocnide</i> <br> -  -  -  -  -  -  -  <i>Dendrocnide elliptica</i> <br> -  -  -  -  -  Rosaceae <br> -  -  -  -  -  -  <i>Prunus</i> <br> -  -  -  -  -  -  -  <i>Prunus javanica</i> <br> -  -  -  -  -  -  <i>Pygeum</i> <br> -  -  -  -  -  -  -  <i>Pygeum beccarii</i> (as synonym: <i>Prunus beccarii</i>)<br> -  -  -  -  -  Moraceae <br> -  -  -  -  -  -  <i>Ficus</i> <br> -  -  -  -  -  -  -  <i>Ficus hispida</i> <br> -  -  -  -  -  -  -  <i>Ficus septica</i> <br> -  -  -  -  -  -  -  <i>Ficus uncinata</i> <br> -  -  -  -  -  -  -  <i>Ficus variegata</i> <br> -  -  -  -  -  -  <i>Antiaris</i> <br> -  -  -  -  -  -  -  <i>Antiaris toxicaria</i> <br> -  -  -  -  -  -  <i>Artocarpus</i> <br> -  -  -  -  -  -  -  <i>Artocarpus anisophyllus</i> <br> -  -  -  -  -  -  -  <i>Artocarpus glaucus</i> <br> -  -  -  -  -  -  -  <i>Artocarpus integer</i> <br> -  -  -  -  -  -  -  <i>Artocarpus odoratissimus</i> <br> -  -  -  -  -  -  -  <i>Artocarpus tamaran</i> <br> -  -  -  -  -  Cannabaceae <br> -  -  -  -  -  -  <i>Trema</i> <br> -  -  -  -  -  -  -  <i>Trema orientalis</i> <br> -  -  -  -  Cornales <br> -  -  -  -  -  Nyssaceae <br> -  -  -  -  -  -  <i>Mastixia</i> <br> -  -  -  -  -  -  -  <i>Mastixia trichotoma</i> <br> -  -  -  -  -  Cornaceae <br> -  -  -  -  -  -  <i>Alangium</i> <br> -  -  -  -  -  -  -  <i>Alangium javanicum</i> <br> -  -  -  -  Gentianales <br> -  -  -  -  -  Apocynaceae <br> -  -  -  -  -  -  <i>Alstonia</i> <br> -  -  -  -  -  -  -  <i>Alstonia angustiloba</i> <br> -  -  -  -  -  Rubiaceae <br> -  -  -  -  -  -  <i>Neonauclea</i> <br> -  -  -  -  -  -  -  <i>Neonauclea gigantea</i> <br> -  -  -  -  -  -  <i>Ludekia</i> <br> -  -  -  -  -  -  -  <i>Ludekia borneensis</i> <br> -  -  -  -  -  -  <i>Psydrax</i> <br> -  -  -  -  -  -  -  <i>Psydrax dicoccos</i> <br> -  -  -  -  -  -  <i>Urophyllum</i> <br> -  -  -  -  -  -  -  <i>Urophyllum polyneurum</i> (as synonym: <i>Pleiocarpidia polyneura</i>)<br> -  -  -  -  -  -  <i>Neolamarckia</i> <br> -  -  -  -  -  -  -  <i>Neolamarckia cadamba</i> <br> -  -  -  -  -  -  <i>Nauclea</i> <br> -  -  -  -  -  -  -  <i>Nauclea subdita</i> <br> -  -  -  -  Fabales <br> -  -  -  -  -  Fabaceae <br> -  -  -  -  -  -  <i>Sindora</i> <br> -  -  -  -  -  -  <i>Crudia</i> <br> -  -  -  -  -  -  -  <i>Crudia reticulata</i> <br> -  -  -  -  -  -  <i>Fordia</i> <br> -  -  -  -  -  -  -  <i>Fordia brachybotrys</i> <br> -  -  -  -  -  -  -  <i>Fordia splendidissima</i> <br> -  -  -  -  -  -  <i>Dialium</i> <br> -  -  -  -  -  -  -  <i>Dialium indum</i> <br> -  -  -  -  -  -  -  <i>Dialium kunstleri</i> <br> -  -  -  -  -  -  <i>Archidendron</i> <br> -  -  -  -  -  -  -  <i>Archidendron clypearia</i> <br> -  -  -  -  -  -  <i>Cynometra</i> <br> -  -  -  -  -  -  -  <i>Cynometra mirabilis</i> <br> -  -  -  -  Sapindales <br> -  -  -  -  -  Meliaceae <br> -  -  -  -  -  -  <i>Chisocheton</i> <br> -  -  -  -  -  -  -  <i>Chisocheton ceramicus</i> <br> -  -  -  -  -  -  -  <i>Chisocheton macranthus</i> <br> -  -  -  -  -  -  -  <i>Chisocheton patens</i> <br> -  -  -  -  -  -  <i>Dysoxylum</i> <br> -  -  -  -  -  -  -  <i>Dysoxylum cyrtobotryum</i> <br> -  -  -  -  -  -  -  <i>Dysoxylum densiflorum</i> <br> -  -  -  -  -  -  <i>Aphanamixis</i> <br> -  -  -  -  -  -  -  <i>Aphanamixis polystachya</i> <br> -  -  -  -  -  -  <i>Lansium</i> <br> -  -  -  -  -  -  -  <i>Lansium domesticum</i> <br> -  -  -  -  -  -  <i>Aglaia</i> <br> -  -  -  -  -  -  -  <i>Aglaia crassinervia</i> <br> -  -  -  -  -  -  -  <i>Aglaia leptantha</i> <br> -  -  -  -  -  -  -  <i>Aglaia macrocarpa</i> <br> -  -  -  -  -  -  -  <i>Aglaia odoratissima</i> <br> -  -  -  -  -  -  -  <i>Aglaia oligophylla</i> <br> -  -  -  -  -  -  -  <i>Aglaia silvestris</i> <br> -  -  -  -  -  -  -  <i>Aglaia tomentosa</i> <br> -  -  -  -  -  Sapindaceae <br> -  -  -  -  -  -  <i>Nephelium</i> <br> -  -  -  -  -  -  <i>Paranephelium</i> <br> -  -  -  -  -  -  -  <i>Paranephelium macrophyllum</i> <br> -  -  -  -  -  -  -  <i>Paranephelium xestophyllum</i> <br> -  -  -  -  -  -  <i>Dimocarpus</i> <br> -  -  -  -  -  -  -  <i>Dimocarpus longan</i> <br> -  -  -  -  -  -  <i>Tristiropsis</i> <br> -  -  -  -  -  -  -  <i>Tristiropsis acutangula</i> <br> -  -  -  -  -  -  <i>Pometia</i> <br> -  -  -  -  -  -  -  <i>Pometia pinnata</i> <br> -  -  -  -  -  Burseraceae <br> -  -  -  -  -  -  <i>Santiria</i> <br> -  -  -  -  -  -  -  <i>Santiria laevigata</i> <br> -  -  -  -  -  -  <i>Canarium</i> <br> -  -  -  -  -  -  -  <i>Canarium decumanum</i> <br> -  -  -  -  -  -  -  <i>Canarium denticulatum</i> <br> -  -  -  -  -  -  -  <i>Canarium odontophyllum</i> <br> -  -  -  -  -  -  -  <i>Canarium pilosum</i> <br> -  -  -  -  -  -  <i>Dacryodes</i> <br> -  -  -  -  -  -  -  <i>Dacryodes rostrata</i> <br> -  -  -  -  -  -  -  <i>Dacryodes rugosa</i> <br> -  -  -  -  -  Rutaceae <br> -  -  -  -  -  -  <i>Melicope</i> <br> -  -  -  -  -  -  -  <i>Melicope confusa</i> <br> -  -  -  -  -  Anacardiaceae <br> -  -  -  -  -  -  <i>Mangifera</i> <br> -  -  -  -  -  -  -  <i>Mangifera odorata</i> <br> -  -  -  -  -  -  <i>Parishia</i> <br> -  -  -  -  -  -  -  <i>Parishia insignis</i> <br> -  -  -  -  -  -  <i>Gluta</i> <br> -  -  -  -  -  -  -  <i>Gluta aptera</i> <br> -  -  -  -  -  -  -  <i>Gluta wallichii</i> <br> -  -  -  -  -  -  <i>Melanochyla</i> <br> -  -  -  -  -  -  -  <i>Melanochyla bullata</i> <br> -  -  -  -  -  -  -  <i>Melanochyla tomentosa</i> <br> -  -  -  -  Laurales <br> -  -  -  -  -  Lauraceae <br> -  -  -  -  -  -  <i>Actinodaphne</i> <br> -  -  -  -  -  -  <i>Beilschmiedia</i> <br> -  -  -  -  -  -  -  <i>Beilschmiedia micrantha</i> <br> -  -  -  -  -  -  <i>Phoebe</i> <br> -  -  -  -  -  -  -  <i>Phoebe grandis</i> <br> -  -  -  -  -  -  <i>Litsea</i> <br> -  -  -  -  -  -  -  <i>Litsea accedens</i> <br> -  -  -  -  -  -  -  <i>Litsea angulata</i> <br> -  -  -  -  -  -  -  <i>Litsea caulocarpa</i> <br> -  -  -  -  -  -  -  <i>Litsea garciae</i> <br> -  -  -  -  -  -  -  <i>Litsea grandis</i> <br> -  -  -  -  -  -  -  <i>Litsea cordata</i> (as synonym: <i>Litsea mappacea</i>)<br> -  -  -  -  -  -  -  <i>Litsea rubiginosa</i> <br> -  -  -  -  -  -  <i>Lindera</i> <br> -  -  -  -  -  -  -  <i>Lindera lucida</i> <br> -  -  -  -  -  -  <i>Eusideroxylon</i> <br> -  -  -  -  -  -  -  <i>Eusideroxylon zwageri</i> <br> -  -  -  -  -  -  <i>Nothaphoebe</i> <br> -  -  -  -  -  -  -  <i>Nothaphoebe umbelliflora</i> <br> -  -  -  -  -  -  <i>Cryptocarya</i> <br> -  -  -  -  -  -  -  <i>Cryptocarya nigra</i> <br> -  -  -  -  -  -  -  <i>Cryptocarya nitens</i> <br> -  -  -  -  -  -  <i>Caryodaphnopsis</i> <br> -  -  -  -  -  -  -  <i>Caryodaphnopsis tonkinensis</i> <br> -  -  -  -  -  -  <i>Dehaasia</i> <br> -  -  -  -  -  -  -  <i>Dehaasia caesia</i> <br> -  -  -  -  -  -  -  <i>Dehaasia incrassata</i> <br> -  -  -  -  Magnoliales <br> -  -  -  -  -  Annonaceae <br> -  -  -  -  -  -  <i>Cyathocalyx</i> <br> -  -  -  -  -  -  <i>Monoon</i> <br> -  -  -  -  -  -  <i>Polyalthia</i> <br> -  -  -  -  -  -  -  <i>Polyalthia obliqua</i> <br> -  -  -  -  -  -  <i>Sageraea</i> <br> -  -  -  -  -  -  -  <i>Sageraea elliptica</i> <br> -  -  -  -  -  -  <i>Miliusa</i> <br> -  -  -  -  -  -  -  <i>Miliusa macropoda</i> <br> -  -  -  -  -  -  <i>Stelechocarpus</i> <br> -  -  -  -  -  -  -  <i>Stelechocarpus cauliflorus</i> <br> -  -  -  -  -  -  <i>Xylopia</i> <br> -  -  -  -  -  -  -  <i>Xylopia ferruginea</i> <br> -  -  -  -  -  -  -  <i>Xylopia stenopetala</i> <br> -  -  -  -  -  -  <i>Phaeanthus</i> <br> -  -  -  -  -  -  -  <i>Phaeanthus splendens</i> <br> -  -  -  -  -  -  <i>Maasia</i> <br> -  -  -  -  -  -  -  <i>Maasia sumatrana</i> <br> -  -  -  -  -  -  <i>Neo-uvaria</i> <br> -  -  -  -  -  -  -  <i>Neo-uvaria acuminatissima</i> <br> -  -  -  -  -  -  <i>Orophea</i> <br> -  -  -  -  -  -  -  <i>Orophea myriantha</i> <br> -  -  -  -  -  -  <i>Pseuduvaria</i> <br> -  -  -  -  -  -  -  <i>Pseuduvaria borneensis</i> <br> -  -  -  -  -  Magnoliaceae <br> -  -  -  -  -  -  <i>Magnolia</i> <br> -  -  -  -  -  -  -  <i>Magnolia borneensis</i> <br> -  -  -  -  -  -  -  <i>Magnolia liliifera</i> <br> -  -  -  -  -  -  -  <i>Magnolia tsiampacca</i> <br> -  -  -  -  -  Myristicaceae <br> -  -  -  -  -  -  <i>Knema</i> <br> -  -  -  -  -  -  -  <i>Knema glauca</i> <br> -  -  -  -  -  -  -  <i>Knema latifolia</i> <br> -  -  -  -  -  -  -  <i>Knema laurina</i> <br> -  -  -  -  -  -  -  <i>Knema oblongata</i> <br> -  -  -  -  -  -  <i>Myristica</i> <br> -  -  -  -  -  -  -  <i>Myristica smythiesii</i> <br> -  -  -  -  -  -  <i>Horsfieldia</i> <br> -  -  -  -  -  -  -  <i>Horsfieldia crassifolia</i> <br> -  -  -  -  Ericales <br> -  -  -  -  -  Primulaceae <br> -  -  -  -  -  -  <i>Ardisia</i> <br> -  -  -  -  -  -  -  <i>Ardisia macrophylla</i> <br> -  -  -  -  -  Lecythidaceae <br> -  -  -  -  -  -  <i>Planchonia</i> <br> -  -  -  -  -  -  -  <i>Planchonia brevistipitata</i> <br> -  -  -  -  -  -  <i>Barringtonia</i> <br> -  -  -  -  -  -  -  <i>Barringtonia lanceolata</i> <br> -  -  -  -  -  -  -  <i>Barringtonia macrostachya</i> <br> -  -  -  -  -  -  -  <i>Barringtonia sarcostachys</i> <br> -  -  -  -  -  Symplocaceae <br> -  -  -  -  -  -  <i>Symplocos</i> <br> -  -  -  -  -  -  -  <i>Symplocos fasciculata</i> <br> -  -  -  -  -  Ebenaceae <br> -  -  -  -  -  -  <i>Diospyros</i> <br> -  -  -  -  -  -  -  <i>Diospyros andamanica</i> <br> -  -  -  -  -  -  -  <i>Diospyros curranii</i> <br> -  -  -  -  -  -  -  <i>Diospyros daemona</i> <br> -  -  -  -  -  -  -  <i>Diospyros dictyoneura</i> <br> -  -  -  -  -  -  -  <i>Diospyros macrophylla</i> <br> -  -  -  -  -  -  -  <i>Diospyros muricata</i> <br> -  -  -  -  -  -  -  <i>Diospyros tuberculata</i> <br> -  -  -  -  -  -  -  <i>Diospyros pilosanthera</i> <br> -  -  -  -  -  Theaceae <br> -  -  -  -  -  -  <i>Pyrenaria</i> <br> -  -  -  -  -  -  -  <i>Pyrenaria tawauensis</i> <br> -  -  -  -  -  Pentaphylacaceae <br> -  -  -  -  -  -  <i>Adinandra</i> <br> -  -  -  -  -  -  -  <i>Adinandra dumosa</i> <br> -  -  -  -  -  Sapotaceae <br> -  -  -  -  -  -  <i>Payena</i> <br> -  -  -  -  -  -  -  <i>Payena acuminata</i> <br> -  -  -  -  -  -  <i>Madhuca</i> <br> -  -  -  -  -  -  -  <i>Madhuca dubardii</i> <br> -  -  -  -  -  -  -  <i>Madhuca korthalsii</i> <br> -  -  -  -  -  -  <i>Palaquium</i> <br> -  -  -  -  -  -  -  <i>Palaquium dasyphyllum</i> <br> -  -  -  -  -  -  -  <i>Palaquium sericeum</i> <br> -  -  -  -  Oxalidales <br> -  -  -  -  -  Elaeocarpaceae <br> -  -  -  -  -  -  <i>Elaeocarpus</i> <br> -  -  -  -  -  -  -  <i>Elaeocarpus floribundus</i> <br> -  -  -  -  -  -  -  <i>Elaeocarpus pedunculatus</i> <br> -  -  -  -  -  -  -  <i>Elaeocarpus stipularis</i> <br> -  -  -  -  -  -  <i>Sloanea</i> <br> -  -  -  -  -  -  -  <i>Sloanea javanica</i> <br> -  -  -  -  Myrtales <br> -  -  -  -  -  Melastomataceae <br> -  -  -  -  -  -  <i>Memecylon</i> <br> -  -  -  -  -  -  -  <i>Memecylon oleifolium</i> <br> -  -  -  -  -  Combretaceae <br> -  -  -  -  -  -  <i>Terminalia</i> <br> -  -  -  -  -  -  -  <i>Terminalia citrina</i> <br> -  -  -  -  -  -  -  <i>Terminalia foetidissima</i> <br> -  -  -  -  -  Myrtaceae <br> -  -  -  -  -  -  <i>Syzygium</i> <br> -  -  -  -  -  -  -  <i>Syzygium chloranthum</i> <br> -  -  -  -  -  -  -  <i>Syzygium elopurae</i> <br> -  -  -  -  -  -  -  <i>Syzygium grande</i> <br> -  -  -  -  -  -  -  <i>Syzygium griffithii</i> <br> -  -  -  -  -  -  -  <i>Syzygium kunstleri</i> <br> -  -  -  -  -  -  -  <i>Syzygium lineatum</i> <br> -  -  -  -  -  -  -  <i>Syzygium panzeri</i> <br> -  -  -  -  -  -  -  <i>Syzygium pustulatum</i> (as synonym: <i>Syzygium perpuncticulatum</i>)<br> -  -  -  -  -  -  -  <i>Syzygium racemosum</i> <br> -  -  -  -  -  -  -  <i>Syzygium rheophyticum</i> <br> -  -  -  -  -  -  <i>Syzygium</i> <br> -  -  -  -  -  -  -  <i>Syzygium chloranthum</i> <br> -  -  -  -  -  -  -  <i>Syzygium elopurae</i> <br> -  -  -  -  -  -  -  <i>Syzygium grande</i> <br> -  -  -  -  -  -  -  <i>Syzygium griffithii</i> <br> -  -  -  -  -  -  -  <i>Syzygium kunstleri</i> <br> -  -  -  -  -  -  -  <i>Syzygium lineatum</i> <br> -  -  -  -  -  -  -  <i>Syzygium panzeri</i> <br> -  -  -  -  -  -  -  <i>Syzygium pustulatum</i> (as synonym: <i>Syzygium perpuncticulatum</i>)<br> -  -  -  -  -  -  -  <i>Syzygium racemosum</i> <br> -  -  -  -  -  -  -  <i>Syzygium rheophyticum</i> <br> -  -  -  -  -  -  <i>Syzygium</i> <br> -  -  -  -  -  -  -  <i>Syzygium chloranthum</i> <br> -  -  -  -  -  -  -  <i>Syzygium elopurae</i> <br> -  -  -  -  -  -  -  <i>Syzygium grande</i> <br> -  -  -  -  -  -  -  <i>Syzygium griffithii</i> <br> -  -  -  -  -  -  -  <i>Syzygium kunstleri</i> <br> -  -  -  -  -  -  -  <i>Syzygium lineatum</i> <br> -  -  -  -  -  -  -  <i>Syzygium panzeri</i> <br> -  -  -  -  -  -  -  <i>Syzygium pustulatum</i> (as synonym: <i>Syzygium perpuncticulatum</i>)<br> -  -  -  -  -  -  -  <i>Syzygium racemosum</i> <br> -  -  -  -  -  -  -  <i>Syzygium rheophyticum</i> <br> -  -  -  -  -  Lythraceae <br> -  -  -  -  -  -  <i>Duabanga</i> <br> -  -  -  -  -  -  -  <i>Duabanga moluccana</i> <br></div><p></p>
Data from Preliminary estimates of genetic parameters and familial selection for non-native poplars show good potential for genetic gains on growth, cold hardiness, trunk quality and Sphaerulina musiva susceptibility
<p>Data from Preliminary estimates of genetic parameters and familial selection for non-native poplars show good potential for genetic gains on growth, cold hardiness, trunk quality and <em>Sphaerulina musiva</em> susceptibility</p> <p><br> Abstract<br> Genetic parameters for growth, trunk quality and susceptibility to frost and <em>Sphaerulina musiva</em> attack was estimated from 34 half-sib families of hybrid poplar from the crossing of non-native parents, <em>Populus maximowiczii</em> A. Henry and <em>Populus trichocarpa</em> Torr. & Gray, 3 and 6 years after planting. The use of spatial analysis proved to be the best method for quantitative growth data. The proportion of the among-family variance to the total (phenotypic) variance as well as the high heritabilities of growth and susceptibility to frost and <em>Spaherulina musiva</em> showed a high potential for selection for these traits while the quality traits were under low genetic control. Some families showed gains for several traits, suggesting the possibility of developing a selection index to obtain superior families that show gain for not only growth but quality and adaptive traits as well. Type B correlations were high, suggesting that families responded in the same way regardless of the site. High type A correlation between growth traits at 3 and 6 years showed early selection potential, although these relationships should be confirmed with future measurements to evaluate this effect at maturity. These results can be integrated into the strategy for improving hybrid poplar parental populations and, in the longer term, will make it possible to optimize the selection of individuals with traits of interest for the operational deployment of hybrid poplar clones.</p>
Randomized Clinical Trial: Expectant Management vs Laser Treatment of Monochorionic Twins With Severe Selective Intrauterine Growth Retardation and Absent or Reverse Diastolic Flow in the Umbilical Ar
ClinicalTrials.gov study NCT01177553. IPD Sharing: Not stated. Countries: 1. Publications: 32.
A Study of Erdafitinib Compared With Vinflunine or Docetaxel or Pembrolizumab in Participants With Advanced Urothelial Cancer and Selected Fibroblast Growth Factor Receptor (FGFR) Gene Aberrations
ClinicalTrials.gov study NCT03390504. IPD Sharing: Not stated. Countries: 27. Publications: 1.
Multi-level in vivo selection of the biocontrol agent Akanthomyces muscarius, virulence, growth, sporulation, and variant data
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Comparative toxicity of larvicides and growth inhibitors on Aedes aegypti from select areas in Jamaica
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Data from: microhabitat selection by the Oscura Mountains Colorado chipmunk (Neotamias quadrivittatus oscuraensis): an old growth pinyon-juniper woodland specialist
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Inter- and intraspecific selection in alien plants: how population growth, functional traits and climate responses change with residence time
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Cheating death: Selection on digestive physiology overcomes expected growth costs of anti-predator defenses
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Data from: Selection for life-history traits to maximize population growth in an invasive marine species
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Short-chain cello-oligosaccharides: Intensification and scale-up of their enzymatic production and selective growth promotion among probiotic bacteria
<p>We provide here the underlying data of the scientific publication "Short-chain cello-oligosaccharides: Intensification and scale-up of their enzymatic production and selective growth promotion among probiotic bacteria". Please find the abstract below:</p> <p>Short-chain cello-oligosaccharides (COS; degree of polymerization, DP≤6) are promising water-soluble dietary fibers. An efficient approach to their bottom-up synthesis is from sucrose and glucose using glycoside phosphorylases. Here, we show intensification and scale up (20 mL; gram scale) of COS production to 93 g/L product and in 82 mol % yield from sucrose (0.5 M). The COS were comprised of DP 3 (33 wt %), DP 4 (34 wt %), DP 5 (24 wt %) and DP 6 (9 wt %) and involved minimum loss (≤10 mol %) to insoluble fractions. After isolation (≥95% purity; ≥90% yield), the COS were examined for growth promotion of probiotic strains. Benchmarked against inulin, trans-galacto-oligosaccharides and cellobiose, COS showed up to 4.1-fold stimulation of cell density for <em>Clostridium butyricum</em>, <em>Lactococcus lactis</em> subsp.<em>lactis</em>, <em>Lactobacillus paracasei</em> subsp. <em>paracasei</em> and <em>Lb. rhamnosus</em> but were less efficient with <em>Bifidobacterium</em> sp. This study shows the COS as selectively functional carbohydrates with prebiotic potential and demonstrates their efficient enzymatic production.</p>
Data from: Growth gains from selective breeding in a spruce hybrid zone do not compromise local adaptation to climate
Hybrid zones contain extensive standing genetic variation that facilitates rapid responses to selection. The Picea glauca x P. engelmannii hybrid zone in western Canada is the focus of tree breeding programs that annually produce ~90 million reforestation seedlings. Understanding the direct and indirect effects of selective breeding on adaptive variation is necessary to implement assisted gene flow polices in Alberta and British Columbia that match these seedlings with future climates. We decomposed relationships among hybrid ancestry, adaptive traits and climate to understand the implications of selective breeding for climate adaptations and assisted gene flow strategies. The effects of selection on associations among hybrid index estimated from ~6500 SNPs, adaptive traits, and provenance climates were assessed for ~2400 common garden seedlings. Hybrid index differences between natural and selected seedlings within breeding zones were small in Alberta (average +2%), but larger and more variable in BC (average -7 %, range -24% to +1%), slightly favoring P. glauca ancestry. The average height growth gain of selected seedlings over natural seedlings within breeding zones was 36% (range 12% to 86%). Clines in growth with temperature-related variables were strong, but differed little between selected and natural populations. Seedling hybrid index and growth trait associations with evapotranspiration-related climate variables were stronger in selected than in natural seedlings, indicating possible pre-adaptation to drier future climates. Associations among cold hardiness, hybrid ancestry and cold-related climate variables dominated signals of local adaptation that were preserved in breeding populations. Strong hybrid ancestry-phenotype-climate associations suggest that assisted gene flow will be necessary to match interior spruce breeding populations with shifting future climates. The absence of antagonistic selection responses among traits and maintenance of cold adaptation in selected seedlings suggests breeding populations can be safely redeployed using assisted gene flow prescriptions similar to those of natural populations.
Data from: The influence of potential stressors on oviposition site selection and subsequent growth, survival and emergence of the non-biting midge (Chironomus tepperi)
Theory predicts that animals should prefer habitats where their fitness is maximized but some mistakenly select habitats where their fitness is compromised, that is, ecological traps. Understanding why this happens requires knowledge of the habitat selection cues animals use, the habitats they prefer and why, and the fitness costs of habitat selection decisions. We conducted experiments with a freshwater insect, the non‐biting midge Chironomus tepperi to ask: (a) whether females respond to potential oviposition cues, (b) to explore whether oviposition is adaptive in relation to metal pollution and conductivity, and (c) whether individuals raised in poor quality sites are more likely to breed in similarly poor locations. We found the following: (a) females responded to some cues, especially conductivity and conspecifics, (b) females preferred sites with higher concentrations of bioavailable metals but suffered no consequences to egg/larval survival, (c) females showed some avoidance of high conductivities, but they still laid eggs resulting in reduced egg hatching, larval survival, and adult emergence, and (d) preferences were independent of natal environment. Our results show that C. tepperi is susceptible to ecological traps, depending on life stage and the relative differences in conductivities among potential oviposition sites. Our results highlight that (a) the fitness outcomes of habitat selection need to be assessed across the life cycle and (b) the relative differences in preference/suitability of habitats need to be considered in ecological trap research. This information can help determine why habitat preferences and their fitness consequences differ among species, which is critical for determining which species are susceptible to ecological traps.
Data from: Horn growth variation and hunting selection of the Alpine ibex
Selective hunting can affect demographic characteristics and phenotypic traits of the targeted species. Hunting systems often involve harvesting quotas based on sex, age and/or size categories to avoid selective pressure. However, it is difficult to assess whether such regulations deter hunters from targeting larger "trophy" animals with longer horns that may have evolutionary consequences. Here, we compile 44,088 annually resolved and absolutely dated measurements of Alpine ibex (Capra ibex) horn growth increments from 8,355 males, harvested between 1978 and 2013, in the eastern Swiss Canton of Grisons. We aim to determine whether male ibex with longer horns were preferentially targeted, causing animals with early rapid horn growth to have shorter lives, and whether such hunting selection translated into long‐term trends in horn size over the past four decades. Results show that medium‐ to longer‐horned adult males had a higher probability of being harvested than shorter‐horned individuals of the same age and that regulations do affect the hunters' behaviour. Nevertheless, phenotypic traits such as horn length, as well as body size and weight, remained stable over the study period. Although selective trophy hunting still occurs, it did not cause a measurable evolutionary response in Grisons' Alpine ibex populations; managed and surveyed since 1978. Nevertheless, further research is needed to understand whether phenotypic trait development is coinfluenced by other, potentially compensatory factors that may possibly mask the effects of selective, long‐term hunting pressure.
Selective area growth of PbTe nanowire networks on InP
<p>data of "Selective area growth of PbTe nanowire networks on InP"</p>
Data from: Positive selection in development and growth rate regulation genes involved in species divergence of the genus Radix
Background: Life history traits like developmental time, age and size at maturity are directly related to fitness in all organisms and play a major role in adaptive evolution and speciation processes. Comparative genomic or transcriptomic approaches to identify positively selected genes involved in species divergence can help to generate hypotheses on the driving forces behind speciation. Here we use a bottom-up approach to investigate this hypothesis by comparative analysis of orthologous transcripts of four closely related European Radix species. Results: Snails of the genus Radix occupy species specific distribution ranges with distinct climatic niches, indicating a potential for natural selection driven speciation based on ecological niche differentiation. We then inferred phylogenetic relationships among the four Radix species based on whole mt-genomes plus 23 nuclear loci. Three different tests to infer selection and changes in amino acid properties yielded a total of 134 genes with signatures of positive selection. The majority of these genes belonged to the functional gene ontology categories "reproduction" and "genitalia" with an overrepresentation of the functions "development" and "growth rate". Conclusions: We show here that Radix species divergence may be primarily enforced by selection on life history traits such as (larval-) development and growth rate. We thus hypothesise that life history differences may confer advantages under the according climate regimes, e.g., species occupying warmer and dryer habitats might have a fitness advantage with fast developing susceptible life stages, which are more tolerant to habitat desiccation.
Selection in space and time: individual tree growth is adapted to tropical forest gap dynamics
<p>In the present study, we assessed genotypic diversity within closely-related sympatric tree species belonging to the widespread tropical tree species complex <em>Symphonia globulifera</em>. We addressed the fine-scale spatial and temporal genetic adaptations of individuals through differential growth strategies in response to forest gap dynamics. We finally compared the breadth of successional niches encountered by <em>Symphonia</em> species to other locally abundant species. Combining tree diameter censuses, indirect measures of light environment of the recent past and present, and single nucleotide polymorphisms (SNPs), we used population genomics, environmental association analyses, genome wide association and growth modelling to address the following questions:</p> <ul> <li>Are individual genotypes structured by the mosaic of light and competition environments resulting from forest gap dynamics?</li> <li>Is the growth of individuals determined by genotypes?</li> <li>Is there an association between genotypic adaptations to gap dynamics and to growth?</li> <li>How are genotypic adaptations to gap dynamics and to growth structured in time, i.e., across life stages?</li> <li>Are breadths of successional niches for <em>Symphonia</em> species wider than those of other locally abundant species?</li> </ul> <p>Find the analyses here : https://sylvainschmitt.github.io/GOING/introduction.html</p>
Selective Fetal Growth Restriction in Monochorionic Twins - an International Investigation
ClinicalTrials.gov study NCT05952583. IPD Sharing: UNDECIDED. Countries: 6. Publications: 0.
Data from: Positive selection in development and growth rate regulation genes involved in species divergence of the genus Radix
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Data from: Faster isn't always better: selection on growth rate fluctuates across the life history and environments
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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.