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357 results for “recession”
Sealing. Oval sealing in terracotta with a one line inscription in an oval cartouche on one side, on the other a small trident before a small inscription stamped in a rectangular recess.
<p>Sealing. Oval sealing in terracotta with a one line inscription in an oval cartouche on one side, on the other a small trident before a small inscription stamped in a rectangular recess. British Museum 2005,0814.20.</p>
Text-fig. 9.—Anterior portion of maxilla of the Jordan theropod (stippled) compared with the corresponding region of the maxillae of other tyrannosaurs. All reproduced to equal length from anterior end of maxilla to anterior margin of antorbital recess (this length in the actual specimens differs by less than 15 percent). A, Juvenile Tyrannosaurus rex. B, Albertosaurus lancensis. C, Juvenile Albertosaurus libratus (AMNH 5664). (A, redrawn from Lawson, 1976; B and C, redrawn from Gilmore, 1946). in A new Theropod Dinosaur from the Upper Cretaceous of Central Montana
Text-fig. 9.—Anterior portion of maxilla of the Jordan theropod (stippled) compared with the corresponding region of the maxillae of other tyrannosaurs. All reproduced to equal length from anterior end of maxilla to anterior margin of antorbital recess (this length in the actual specimens differs by less than 15 percent). A, Juvenile Tyrannosaurus rex. B, Albertosaurus lancensis. C, Juvenile Albertosaurus libratus (AMNH 5664). (A, redrawn from Lawson, 1976; B and C, redrawn from Gilmore, 1946).
Text-fig. 7.—A, Ratio (H/L) of height of maxilla (at anterior margin of antorbital recess) to length of maxilla (to anterior margin of antorbital recess), plotted against length (L) of maxilla (to anterior margin of antorbital recess). Length scale in cm. B, Ratio (D/L) of depth of dentary ramus to length of maxilla (to anterior margin of antorbital recess), plotted against length of maxilla (to anterior margin of antorbital recess). Length scale in cm. in A new Theropod Dinosaur from the Upper Cretaceous of Central Montana
Text-fig. 7.—A, Ratio (H/L) of height of maxilla (at anterior margin of antorbital recess) to length of maxilla (to anterior margin of antorbital recess), plotted against length (L) of maxilla (to anterior margin of antorbital recess). Length scale in cm. B, Ratio (D/L) of depth of dentary ramus to length of maxilla (to anterior margin of antorbital recess), plotted against length of maxilla (to anterior margin of antorbital recess). Length scale in cm.
Kirkmichael, Arched recess tomb
The 1584 arched recess tomb of John Urquhart at Kirkmichael. Further information can be found at: http://www.kirkmichael.info/ArchedTombRecess.html Source: Objaverse 1.0 / Sketchfab
Extended incubation recesses in Sanderlings are impacted by temperature and body condition
<p>Complex incubation strategies have evolved to solve the trade-off between parent survival and care for their eggs with often brief departures (recesses) that maximise egg survival or infrequent extended recesses maximising adult condition. Here we examined incubation behaviour of Sanderlings (<em>Calidris alba</em>), a species that exhibits both bi- and uniparental incubation behaviour. During 11 breeding seasons in Greenland, we have quantified incubation variability with thermologgers placed in nests. We estimated the impact of environmental conditions and individual characteristics on the occurrence and the duration of recesses. We found that extended recesses are a unique feature of uniparentals, and their frequency and duration increased in colder temperatures. The relationship was mediated by body condition, with individuals in poor condition performing longer extended recesses in colder temperatures. This suggests that extended recesses may represent a shift towards self-maintenance at the expense of the egg care, allowing birds to continue incubating under unfavourable conditions. Our study illustrates how extended recesses may be a key breeding strategy to overcome high energetical costs associated with incubation. Quantifying such behavioural flexibility paves the way for tracking future behavioural responses of individuals in the face of changing environments.</p>
Input and Output files for "Contributions to Streamflow and Sea Level Rise in High Mountain Asia from 2003-2009 Glacier Recession"
<p>All files below were prepared by Collin B. Lawrence. </p> <p>All ARCIDs correspond to the HydroSHEDS Dataset for Asia (Lehner et al., 2008). (http://www.hydrosheds.org/)</p> <p>GLDAS data are from the Global Land Data Assimilation System (Rodell et al., 2004). (https://ldas.gsfc.nasa.gov/gldas/)</p> <p>Q_JJA_(model) contains three columns: 1) ARCID, 2) subsurface and surface runoff for that particular reach, and 3) accumulated subsurface and surface runoff. All flows are in m<sup>3</sup> s<sup>-1</sup>, and are averaged for the months of June, July, and August from the years 2003 – 2009. CLM, MOSAIC, NOAH, and VIC were the subset of models used from the Global Land Data Assimilation System (GLDAS).</p> <p>Q_annual_(model) contains three columns: 1) ARCID, 2) subsurface and surface runoff for that particular reach, and 3) accumulated subsurface and surface runoff. All flows are in m<sup>3</sup> s<sup>-1</sup>, and are yearly averages for the years 2003 – 2009. CLM, MOSAIC, NOAH, and VIC were the subset of models used from the Global Land Data Assimilation System (GLDAS).</p> <p>phi_i_JJA is the accumulated subsurface and surface runoff for the CLM, MOSAIC, NOAH, and VIC model average. The June, July, and August output was averaged over the years 2003 – 2009. Column 1 is ARCID and the accumulated runoff is expressed in m<sup>3</sup> s<sup>-1</sup>.</p> <p>phi_i_JJA_err is the standard error of the model mean in phi_i_JJA.</p> <p>phi_g_JJA contains the accumulated glacier recession flow in m<sup>3</sup> s<sup>-1 </sup>for the months of June, July, August from 2003 - 2009.</p> <p>phi_g_JJA_err is the standard error of the model mean in phi_g_JJA.</p> <p>phi_g_annual contains the annually averaged accumulated glacier recession flow in m<sup>3</sup> s<sup>-1 </sup>for 2003 – 2009.</p> <p>lambda.csv contains the fraction of streamflow from glacier recession.</p>
Potential for shoreline recession to accelerate discharge of groundwater pollutants to coastal waters
<p>Included in this repository are supporting field data used to produce the results of the manuscript submitted to Water Resources Research:</p> <p>Sabina Rakhimbekova, Christopher Power, Denis M. O’Carroll, Clare E. Robinson, (2023) "<strong>Potential for shoreline recession to accelerate discharge of groundwater pollutants to coastal waters"</strong></p>
Data for: Climate change alone cannot explain boreal caribou range recession in Quebec since 1850
<p><span>The contraction of species range is one of the most significant symptoms of biodiversity loss worldwide. While anthropogenic activities and habitat alteration are major threats for several species, climate change has not been overlooked either. For species at risk, differentiating the effects of human disturbances and climate change on past and current range transformations is an important step towards improved conservation strategies. We paired historical range maps with global atmospheric reanalyses from different sources (ERA5, CERA-20C, 20CRv3) to assess the potential effects of recent climate change on the observed northward contraction of the distribution range of boreal populations of woodland caribou (<em>Rangifer tarandus caribou</em>) in Quebec (Canada) since 1850. We quantified these effects by highlighting the discrepancies between different southern limits of the caribou's range (used as references) observed in the past and reconstitutions obtained through the hindcasting of the climate conditions within which caribou are currently found. Hindcasted southern limits moved ~105 km north over time under all reanalysis datasets, a trend drastically different from the ~620 km reported for observed southern limits since 1850. The differences in latitudinal shift through time between the observed and hindcasted southern limits of distribution suggest that caribou range recession should have been only 17% of what has been observed since 1850 if recent climate change had been the only disturbance driver. This limited impact of climate reinforces the scientific consensus stating that caribou range recession in Quebec is mainly caused by anthropogenic drivers (i.e. logging, development of the road network, agriculture, urbanization) that have modified the structure and composition of the forest over the past 160 years, paving the way for habitat-mediated apparent competition and overharvesting. Our results also call for a better consideration of past distribution ranges in models aiming at projecting future distributions, especially for endangered species.</span></p>
Augmented Medial Rectus Muscle Recession Versus Posterior Scleral Fixation in Partially Accommodative Esotropia
ClinicalTrials.gov study NCT02413463. IPD Sharing: Not stated. Countries: 1. Publications: 2.
Gene Transfer for Recessive Dystrophic Epidermolysis Bullosa
ClinicalTrials.gov study NCT01263379. IPD Sharing: YES. Countries: 1. Publications: 3.
VO2 Max: In Vivo Model for Functional Red Cell Testing. Can RECESS be Explained?
ClinicalTrials.gov study NCT02918851. IPD Sharing: NO. Countries: 1. Publications: 1.
Effectiveness of Modified-free Gingival Graft for Treatment of Localized Gingival Recession Defects
ClinicalTrials.gov study NCT04718545. IPD Sharing: NO. Countries: 1. Publications: 6.
Bilateral Lateral Rectus Recession Versus Unilateral Recess-Resect for Intermittent Exotropia
ClinicalTrials.gov study NCT01032603. IPD Sharing: YES. Countries: 1. Publications: 5.
Using Calcium Hydroxylapatite To Treat Gum Recession and Tooth Hypersensitivity
ClinicalTrials.gov study NCT06826391. IPD Sharing: YES. Countries: 1. Publications: 7.
Pinhole Surgical Technique Compared to Connective Tissue Graft in Treatment of Gingival Recession
ClinicalTrials.gov study NCT04356391. IPD Sharing: NO. Countries: 1. Publications: 21.
Use of Platelet Rich Fibrin in Addition to CAF and SCTG for Treatment of Gingival Recession
ClinicalTrials.gov study NCT03199118. IPD Sharing: NO. Countries: 1. Publications: 14.
Data for: Climate change alone cannot explain boreal caribou range recession in Quebec since 1850
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Data from: A SACS deletion variant in Great Pyrenees dogs causes autosomal recessive neuronal degeneration
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Extended incubation recesses in Sanderlings are impacted by temperature and body condition
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Fine mapping highlights ITGAL and MUS81 loss-of-function mutations modulating recessive impacts in dairy cattle
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Allen Brain Atlas
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