132,096 research outputs found
Lyons & McClelland 2022
No full textNaming Legend for Lyons & McClelland 2022 Data files.
ha = highlander
la= lowlander
wn = warm normoxia
ch = cold hypoxia
r = resting
ps = vo2max
All analyses were performed using lme4 package in R v.4.0.0.
We use 2-way analysis of variance to assess main effects of population (highlander vs lowlander) and either acclimation environment (warm normoxia vs cold hypoxia), or activity condition (resting vs vo2max).
We also used a 3-way analysis of variance to assess population, acclimation and activity condition where appropriate.
Data was collected over the course of 2020-2021 at McMaster University.
Below are breakdown of the figures and tables and the data files accociated with each.
Figure 1. Rate of glycerol release from inguinal white adipose tissue (ingWAT).
:Lyons & McClelland 2022 white adipose tissue glycerol release.csv
Figure 2. Plasma concentrations of glycerol (A), non-esterified fatty acids (NEFA) (B), and triglycerides (TG) at rest and at cold-induced V̇O2max (C).
:Lyons & McClelland 2022 rest vs vo2max plasma glycerol.csv
:Lyons & McClelland 2022 rest vs vo2max plasma fatty acids.csv
:Lyons & McClelland 2022 rest vs vo2max plasma triglycerides.csv
Figure 3. Plasma flow rate (A) non-esterified fatty acid (NEFA) delivery rate (B) and triglyceride (TG) delivery rate (C) at cold-induced V̇O2max in hypoxia.
:Lyons & McClelland 2022 vo2max plasma delivery rate.csv
Figure 4. Intramuscular triglyceride (TG) concentration during rest and immediately after cold-induced V̇O2max.
:Lyons & McClelland 2022 rest vs vo2max imtg.csv
Figure 5. Relative protein abundance of fatty acid translocase (FAT/CD36) in brown adipose tissue.
:Lyons & McClelland 2022 brown adipose tissue cd36.csv
Figure 6. Total protein abundance of fatty acid translocase (FAT/CD36) (A), sarcolemmal fraction FAT/CD36 abundance at cold-induced V̇O2max (B) and fatty acid binding protein (FABP) abundance (C) in the gastrocnemius.
:Lyons & McClelland 2022 whole gastrocnemius cd36.csv
:Lyons & McClelland 2022 gastrocnemius sarcolemmal cd36.csv
:Lyons & McClelland 2022 gastrocnemius fatty acid binding protein.csv
Figure 7. Apparent maximal enzyme activities (Vmax) of carnitine palmitoyl transferase (CPT) in isolated muscle mitochondria (A), and ß-hydroxyacyl-CoA dehydrogenase (HOAD) (B), citrate synthase (CS) (C), and cytochrome c oxidase (COX) (D) in the gastrocnemius.
:Lyons & McClelland 2022 gastrocnemius cpt enzyme activity.csv
:Lyons & McClelland 2022 gastrocnemius hoad and cox enzyme activity.csv
:Lyons & McClelland 2022 gastrocnemius citrate synthase enzyme activity.csv
Figure S1. Exogenous fatty acid oxidation rates of soleus muscle.
:Lyons & McClelland 2022 soleus exogenous lipid oxidation.csv
Table 1. Body mass, inguinal white adipose tissue (ingWAT) mass and ingWAT mass relative to body mass of first-generation laboratory born and raised highland and lowland deer mice (Peromyscus maniculatus), acclimated to control warm normoxia (23oC, 12 kPa O2) or cold hypoxia (5oC, 12 kPa O2) conditions.
:Lyons & McClelland 2022 relative white adipose tissue mass.csv
Table 2. Concentrations of individual plasma fatty acids (µmol L-1) of first-generation laboratory born and raised highland and lowland deer mice (Peromyscus maniculatus), acclimated to control warm normoxia (23oC, 12 kPa O2) or cold hypoxia (5oC, 12 kPa O2) conditions, during rest and cold-induced V̇O2max.
:Lyons & McClelland 2022 rest vs vo2max plasma fatty acids.csv</p
Lamellilatirus Lyons & Snyder 2008
No full textGenus Lamellilatirus Lyons & Snyder, 2008 Type species. Fusus ceramidus Dall, 1889, Recent, Barbados, by original designation (Lyons & Snyder, 2008: 236). Diagnosis. Shell: small to medium size, fusiform, light-weight, with columellar folds faint or (usually) lacking and with abundant scale-like lamellae on sutural ramp. Radula: rachidian tooth subquadrate, longer than wide, with 3 forward-directed cusps, median cusp longest; lateral tooth wide, with single small cusp at medial edge, flanked by larger, mesially slanting saw-toothed cusps; much smaller cusp near lateral margin separated from others by wide gap (Lyons & Snyder 2008: 228, fig. 3a, after Bullock 1968). Remarks. Absence of columellar folds is common among genera of Fusininae but also occurs among some genera of Peristerniinae, e.g. the Indo-west Pacific genus Fusolatirus Kuroda & Habe, 1971, but the radula of Fusolatirus has alternating long and short cusps on lateral teeth (Kuroda & Habe 1971: 182). Bullock (1968: pl. 8) figured radulae of several Western Atlantic species of Peristerniinae now in Polygona Schumacher, 1817, Hemipolygona Roveretto, 1899, Pustulatirus Vermeij & Snyder, 2006, Bullockus Lyons & Snyder, 2008 and Lamellilatirus. Of these, the Lamellilatirus radula resembles those of species now classified in Pustulatirus, but shells of that genus have distinct columellar folds (Lyons & Snyder 2013a). The Lamellilatirus radula also resembles those of some species of the Indo-west Pacific genus Benimakia Habe, 1958 (see Bouchet & Snyder 2012: figs. 3A–F), but shells of that genus have a labral tooth that is absent in Lamellilatirus. In studies of molecular phylogeny of Fasciolariidae (Couto et al. 2016: 314, 315; Kantor et al. 2018: 4, 14), a species of Lamellilatirus from French Guiana (IM 2013-56511) grouped with species of Latirus Montfort, 1810, Leucozonia Gray, 1847 and Polygona Schumacher, 1817 (genera customarily placed in Peristerniinae), not with genera of Fusininae. Five species of Lamellilatirus have been described: L. ceramidus (Dall, 1889) and L. dominiquei, L. eburneus, L. lamyi and L. sunderlandorum, all of Lyons and Snyder, 2013. Species of Lamellilatirus were known previously only in the southern Caribbean Sea, ranging from Puerto Rico and Honduras southward to Venezuela. Two new species described here extend the range of the genus to northeastern South America.Published as part of Lyons, William G. & Snyder, Martin Avery, 2019, Fasciolariidae (Gastropoda: Neogastropoda) of French Guiana and nearby regions, with descriptions of two new species and comments on marine zoogeography of northeastern South America, pp. 239-268 in Zootaxa 4585 (2) on pages 254-255, DOI: 10.11646/zootaxa.4585.2.2, http://zenodo.org/record/263730
Lyons, L J, NX60128
No full textThis record was harvested from a previous catalogue system and will be withdrawn in 2025. Information in this record may be superseded or incomplete. Visit this record in UMA's new catalogue at: https://archives.library.unimelb.edu.au/nodes/view/400499Surname: LYONS. Given Name(s) or Initials: L J. Military Service Number or Last Known Location: NX60128. Missing, Wounded and Prisoner of War Enquiry Card Index Number: 24769.219028
Item: [2016.0049.32792] "Lyons, L J, NX60128
Double-devolution or double-dealing? : the local government White Paper and the Lyons review
No full textNew Labour's third White Paper promised the revitalization of local government after ten years of control freakery. It does not, however, live up to the promise of a 'new localism'. The tenor of the paper is moralising and prescriptive, claims to a new approach belied by the government's negative response to Lyons. Proposals for reform are ambiguous, offering no guarantees against back-door centralisation. Such cause as there may be for optimism largely depends on the capacity of localities to take the initiative. A fundamental debate about the role of local government, local democracy and the relationship between centre and locality is therefore still needed. Given the preponderance of path dependencies, strategic dilemmas and structural constraints upon the centre, the demand for local democracy will have to be initiated, voiced and organised by local citizens and councillors themselves
Marriage record of Lyons, Allen L. and Smith, Bessie L.
No full textMarriage license for Allen L. Lyons and Bessie L. Smith. W.P. Head was the officiant
Pat J. L. Lyons Park, Mobile, Alabama
No full textColor print of Pat J. L. Lyons Park, located on Spring Hill Avenue in Mobile, AL. Defined walking paths. Open pavillion and other buildings in background. Landscaped with flowers and trees. Park was named for the 40th mayor for the city of Mobile. Afternoon sunset sky. Divided back postcard.Printed on front: ' Pat J. L. Lyons Park, Springhill Ave., Mobile, Ala.' Printed on back: 'C. T. American Art.
Land-atmosphere interactions in Southwest Western Australia
No full textThe Southwest of Western Australia (SWWA) is a region of extensive land cover change with an estimated 13 million hectares of native vegetation cleared since European settlement. Whilst previous studies have suggested meteorological and climatological implications of this change in land use, no studies have explicitly focussed on the detailed mechanisms behind the impacts of land-cover change on individual meteorological phenomena. This thesis seeks to identify the physical mechanisms inducing changes within the atmosphere by using the Regional Atmospheric Modeling System (RAMS V6.0) to simulate the impact of land use change on meteorological phenomena at different scales and evaluate these model results against high resolution atmospheric soundings, station observations, and gridded rainfall analyses where appropriate. Sensitivity tests show that land-cover change results in an increase in low-level atmospheric moisture advection associated with the southern sea-breeze due to a reduction in surface roughness. It also results in a decrease in convective precipitation associated with cold-fronts and convective clouds associated with the surface heat trough, due to an increase in wind speed, and a decrease in turbulent kinetic energy and vertically integrated moisture convergence within the PBL. Large-eddy simulations further highlight the role of land-cover change and soil moisture, as well as the contributions of surface versus entrainment fluxes on the growth of the PBL and development of convective clouds. These results are discussed within the broader context of the meteorology of the region
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