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89 results for “lability”
Dataset and Code: Lability in Balkan Slavic
<p>This is a dataset for the article: Makartsev, Maxim; Wahlström, Max and Anastasia Escher. 2025. "Lability in Balkan Slavic," <em>Studies in Language 49</em> [Special issue: “Areal Effects in Argument-Coding Patterns”]</p> <p><span>Abstract: The article assesses claims made in the previous studies regarding the increase in the number of identical transitive and intransitive verbs with patient-like arguments, that is, patientively labile (P-labile) verbs, in Macedonian in comparison with the other South Slavic languages. Based on an extensive sample of 130 varieties from different parts of the South Slavic dialectal continuum, this study confirms the observations regarding increased lability in Western and some Southeastern Macedonian dialects. Additionally, outside the labile hotbed, lability remains low with relatively homogenous patterning.</span></p> <p><span>Keywords: lability, </span>causativity<span>, Balkan linguistics, South Slavic dialectology, language contact.</span></p>
Herbarium specimen image of Eucryphia lucida (Labill.) Baill., part of the collection of Meise Botanic Garden
Part of a training dataset of scanned herbarium specimens. The data paper and a summary landing page will be published on Zenodo as it gets published.<br><br>Content of this deposition:<br><br>- A JSON-LD datafile listing the label data associated with this herbarium specimen. The Darwin and Dublin Core data standards are used for most values.<br>- A JPEG image file of the scanned herbarium sheet.<br>- A lossless TIFF image from which the JPEG image has been derived.
Data from: Efficacy of labile carbon addition to reduce fast-growing, invasive non-native plants: A review and meta-analysis
<p>Data and analysis in R for the publication "Efficacy of labile carbon addition to reduce fast-growing, invasive non-native plants: A review and meta-analysis" by Ossanna & Gornish (2023), <em>Journal of Applied Ecology</em>, <em>60</em>(2), 218-228. <a href="http://doi.org/10.1111/1365-2664.14324">https://doi.org/10.1111/1365-2664.14324</a>.</p>
Stable isotope and conservative tracer data used to estimate uptake of stream water dissolved organic carbon (DOC) through a whole-stream addition of a ¹³C-DOC tracer coupled with laboratory measurements of bioavailability of the tracer and stream water DOC using lability profiling with bioreactors
We performed a whole-stream addition of a ¹³C-DOC tracer and made laboratory measurements of the biological availability of the tracer as well as stream water DOC. The study was performed in October 2002 in a 1.27 km stretch of the third-order White Clay Creek in southeastern Pennsylvania. The tracer was prepared as a cold-water leachate of ¹³C-labeled tulip poplar saplings and it was added to the stream along with sodium bromide, a conservative tracer, over a 2-h period. Stream water samples were collected at 8 downstream stations over an 8-h period, filtered, and analyzed for concentrations of bromide and DOC. DOC was measured by Pt-catalyzed, persulfate oxidation, Br- was analyzed by ion chromatography, and C isotope samples were rotary evaporated, acidified, lyophilized, combusted, and the CO₂ analyzed with an elemental analyzer interfaced with an isotope ratio mass spectrometer. Lability profiling of the ¹³C-DOC tracer and stream water DOC were performed with a series of plug-flow bioreactors of increasing empty-bed contact times with the concentration of biodegradable DOC operationally defined as the difference between the DOC concentrations in the influent and effluent waters of the bioreactors. The bioreactor measurements were performed 2 days after the whole-stream release. Data were analyzed to estimate the uptake of stream water DOC associated with labile and semi-labile fraction of biodegradable DOC. These data have been previously used in a 2008 publication in Freshwater Biology, doi:10.1111/j.1365-2427.2007.01941.x.
Dataset: Bacterioplankton metabolism of phytoplankton lysates across a cyclone-anticyclone eddy dipole impacts the cycling of semi-labile organic matter in the photic zone
<p>This dataset contains both field data and the results of dilution batch-culture bioassay experiments characterizing bacterioplankton usage of ambient and added dissolved organic matter across a cyclone to anticyclone spatial transect in the North Pacific Subtropical Gyre. Field data include total organic carbon, total nitrogen, bacterioplankton cell abundances, ammonia monooxygenase subunit A gene concentrations, and 16S rRNA gene amplicons. Experimental data include time-resolved changes in total organic carbon, nitrogen species, and bacterioplankton cell abundances.</p>
FIG. 1 in Lectotypification of the name Lomandra longifolia Labill. (Asparagaceae: Lomandroideae)
FIG. 1. — Lectotype specimen of Lomandra longifolia Labill. in the Herbarium Universitatis Florentinae (FI012018). Image from JSTOR Global Plants and © SMA, Museo di Storia Naturale, Collezioni Botaniche, Florence with acknowledgements.
Shifts in evolutionary lability underlie independent gains and losses of root-nodule symbiosis in a single clade of plants
<p><span>Supplementary Data 4 from the manuscript "Shifts in evolutionary lability underlie independent gains and losses of root-nodule symbiosis in a single clade of plants". </span></p> <p><span>A concatenated alignment of all samples and all loci. This file was used for branch length estimation and not directly for phylogeny reconstruction (though an extraction of each subtree taxonomic samples subset from this alignment would be the alignment used to produce the scaffolded subtrees that were described in the paper). Sequences are labeled by well and can be mapped back to taxon for sub-setting and further use using Supplementary Data 1. </span></p>
Data for "Excess labile carbon promotes the expression of virulence factors in coral reef bacterioplankton"
<p>This publication contains 27 coral reef bacterioplankton metagenome-assembled genomes (MAGs) from the following paper: </p> <p>Cárdenas, A., Neave, M. J., Haroon, M. F., Pogoreutz, C., Rädecker, N., Wild, C., Gärdes, A., & Voolstra, C. R. (2018). Excess labile carbon promotes the expression of virulence factors in coral reef bacterioplankton. <em>The ISME Journal</em>, <em>12</em>(1), 59–76. https://doi.org/10.1038/ismej.2017.142</p> <p> </p>
Daucus glochidiatus (Labill.) Fisch., C.A.Mey. & Avé-Lall. (BR0000014439094)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Juniperus drupacea Labill. (BR0000025050080)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Juniperus drupacea Labill. (BR0000009237568)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Juniperus drupacea Labill. (BR0000025050097)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Juniperus drupacea Labill. (BR0000025050073)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Linked collectors and determiners for: Lectotypification of the name Lomandra longifolia Labill. (Asparagaceae: Lomandroideae).
Natural history specimen data linked to collectors and determiners held within, "Lectotypification of the name Lomandra longifolia Labill. (Asparagaceae: Lomandroideae)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/af2cc352-39a9-42ee-94fc-235d1f65677f">https://bionomia.net/dataset/af2cc352-39a9-42ee-94fc-235d1f65677f</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/af2cc352-39a9-42ee-94fc-235d1f65677f">https://gbif.org/dataset/af2cc352-39a9-42ee-94fc-235d1f65677f</a>. Formatted as a Frictionless Data package.
Bromus arenarius Labill. (BR0000011489627)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
FIG. 1 in Kwanghwana miscanthi Karun., C.H.Kuo & K.D.Hyde, gen. et sp. nov. (Phaeosphaeriaceae, Pleosporales) on Miscanthus floridulus (Labill.) Warb. ex K.Schum. & Lauterb. (Poaceae)
FIG. 1. — Phylogram generated from RAxML analysis based on a combined dataset of LSU, SSU, ITS and TEF1-α partial sequences. Bootstrap support values for maximum likelihood higher than 60% and Bayesian posterior probabilities (BYPP) greater than 0.90 are displayed as above the nodes respectively. The extype strains are in bold. New strain is indicated in red. The tree is rooted to Leptosphaeria doliolum (Pers.) Ces. & De Not. (CBS 505.75) and Paraleptosphaeria dryadis (Johanson) Gruyter, Aveskamp & Verkley (CBS 643.86).
FIG. 2 in Kwanghwana miscanthi Karun., C.H.Kuo & K.D.Hyde, gen. et sp. nov. (Phaeosphaeriaceae, Pleosporales) on Miscanthus floridulus (Labill.) Warb. ex K.Schum. & Lauterb. (Poaceae)
FIG. 2.— Kwanghwana miscanthi Karun., C.H.Kuo & K.D.Hyde, sp. nov. (MFU 18-1950, holotype): A, B, appearance of ascomata on the host Miscanthus floridulus (Labill.) Warb. ex K.Schum. & Lauterb. (Poaceae) leaf sheath; C, section through ascoma; D, section through peridium at the apex; E, section through peridium at the base; F, hamathecium; G, Pseudoparaphyses; H-K, asci; L-P, ascospores; Q, germinating ascospore; R, S, culture characteristics on PDA (r = from above, s = from below). Scale bars: C, 20 µm; D-F, 25 µm; G-K, 20 µm; L-Q, 25 µm.
Fig. 8 in Morphological trait evolution in Solanum (Solanaceae): Evolutionary lability of key taxonomic characters
Fig. 8. Evolution of the most conserved morphological traits in Solanum with <10 transitions based on species-level analysis using stochastic character mapping. A, Pseudostipules; B, Enlarged anther connectives; C, Anther modifications; D, Pedicel insertion. Results from the best model are shown for each character (see Table 1 and suppl. Table S4 for details) based on 200 simulations. The topology used for mapping was derived from a supermatrix phylogeny with nine loci (two nuclear and seven plastid loci; Gagnon & al., 2022) with 725 species sampled and coded for each trait (58% of all species). All minor clades are labelled; tips reflect the crown nodes of each minor clade. Piecharts indicate likelihood of modelled ancestral states along the nodes, and frequency bars (tips) reflect proportion of species sampled within each clade with each state.
Fig. 4 in Morphological trait evolution in Solanum (Solanaceae): Evolutionary lability of key taxonomic characters
Fig. 4. Evolution of the most highly labile morphological traits in Solanum with>100 transitions based on species-level analysis using stochastic character mapping. A, Growth form; B, Sympodial unit structure; C, Glandular trichomes; D, Corolla shape; E, Corolla colour; F, Fruit colour. Results from the best model are shown for each character (see Table 1 and suppl. Table S4 for details) based on 200 simulations. The topology used for mapping was derived from a supermatrix phylogeny with nine loci (two nuclear and seven plastid loci; Gagnon & al., 2022) with 725 species sampled and coded for each trait (58% of all species). All minor clades are labelled; tips reflect the crown nodes of each minor clade. Piecharts indicate likelihood of modelled ancestral states along the nodes, and frequency bars (tips) reflect proportion of species sampled within each clade with each state.
Data from: Evolutionary lability of sexual selection and its implications for speciation and macroevolution
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