115 research outputs found
Angular distributions of H-induced HD and D2 desorptions from the Si(100) surfaces
We measured angular distributions of HD and D2 molecules desorbed via the reactions H+D/Si 100 âHD abstraction ABS and H+D/Si 100 âD2 adsorption-induced-desorption AID , respectively. It was found that the angular distribution of HD molecules desorbed alongABS is broader than that of D2 molecules desorbed along AID, i.e., the former could be fit withcos2.0±0.2 , while the latter with cos5.0±0.5 . This difference of the angular distributions between thetwo reaction paths suggests that their dynamic mechanisms are different. The observed cos2 distribution for the ABS reaction was reproduced by the classical trajectory calculations over theLondon-Eyring-Polanyi-Sato potential-energy surfaces. The simulation suggests that the HDdesorption along the ABS path takes place along the direction of SiâD bonds, but the apparentangular distribution is comprised of multiple components reflecting the different orientations ofD-occupied Si dimers in the 2 1 and 1 2 double domain structures
Modulated hydrogen beam study of adsorption-induced desorption of deuterium from Si(100)-3Ă1:D surfaces
We have studied the kinetic mechanism of the adsorption-induced-desorption (AID) reaction, H + D/Si(100)D2. Using a modulated atomic hydrogen beam, two different types of AID reaction are revealed: one is the fast AID reaction occurring only at the beam on-cycles and the other the slow AID reaction occurring even at the beam off-cycles. Both the fast and slow AID reactions show the different dependence on surface temperature Ts, suggesting that their kinetic mechanisms are different. The fast AID reaction overwhelms the slow one in the desorption yield for 300 KTs650 K. It proceeds along a first-order kinetics with respect to the incident H flux. Based on the experimental results, both two AID reactions are suggested to occur only on the 3Ă1 dihydride phase accumulated during surface exposure to H atoms. Possible mechanisms for the AID reactions are discussed
Exploration and Comparison of Physical Mechanisms Related to the Dynamic Evolution of Density Profiles in the Toroidal Confinement Devices
Deaf readers benefit from lexical feedback during orthographic processing
It has been proposed that poor reading abilities in deaf readers might be related to weak connections between the orthographic and lexical-semantic levels of processing. Here we used event related potentials (ERPs), known for their excellent time resolution, to examine whether lexical feedback modulates early orthographic processing. Twenty congenitally deaf readers made lexical decisions to target words and pseudowords. Each of those target stimuli could be preceded by a briefly presented matched-case or mismatched-case identity prime (e.g., ALTAR-ALTAR vs. altar- ALTAR). Results showed an early effect of case overlap at the N/P150 for all targets. Critically, this effect disappeared for words but not for pseudowords, at the N250âan ERP component sensitive to orthographic processing. This dissociation in the effect of case for word and pseudowords targets provides strong evidence of early automatic lexical-semantic feedback modulating orthographic processing in deaf readers. Interestingly, despite the dissociation found in the ERP data, behavioural responses to words still benefited from the physical overlap between prime and target, particularly in less skilled readers and those with less experience with words. Overall, our results support the idea that skilled deaf readers have a stronger connection between the orthographic and the lexical-semantic levels of processing
Raising the Bar: Improving Methodological Rigour in Cognitive Alcohol Research
Background and Aims: A range of experimental paradigms claim to measure the cognitive processes underpinning alcohol use, suggesting that heightened attentional bias, greater approach tendencies and reduced cue-specific inhibitory control are important drivers of consumption. This paper identifies methodological shortcomings within this broad domain of research and exemplifies them in studies focused specifically on alcohol-related attentional bias. Argument and analysis: We highlight five main methodological issues: (i) the use of inappropriately matched control stimuli; (ii) opacity of stimulus selection and validation procedures; (iii) a credence in noisy measures; (iv) a reliance on unreliable tasks; and (v) variability in design and analysis. This is evidenced through a review of alcohol-related attentional bias (64 empirical articles, 68 tasks), which reveals the following: only 53% of tasks use appropriately matched control stimuli; as few as 38% report their stimulus selection and 19% their validation procedures; less than 28% used indices capable of disambiguating attentional processes; 22% assess reliability; and under 2% of studies were pre-registered. Conclusions: Well-matched and validated experimental stimuli, the development of reliable cognitive tasks and explicit assessment of their psychometric properties, and careful consideration of behavioural indices and their analysis will improve the methodological rigour of cognitive alcohol research. Open science principles can facilitate replication and reproducibility in alcohol research
Synthesis of calcitonin gene-related peptide (CGRP) by rat arterial endothelial cells
We investigated the protein and mRNA expression of calcitonin gene-related peptide (CGRP) in endothelial cells of the rat thoracic aorta and femoral artery. Light microscopic immunocytochemistry revealed that immunoreactivity for CGRP was preferentially located in the endothelium of both vessels. Immunoelectron microscopy showed that CGRPimmunoreactive gold particles were preferentially localized on cisterns of the rough endoplasmic reticulum and on the Weibel-Palade (WP) bodies in the endothelial cells. Prepro CGRP mRNA signals were also detected on the endothelium. Our results are the first to demonstrate that endothelial cells of both elastic and large muscular arteries synthesize CGRP and store it, in part, in WP bodies, implying that CGRP may act as an endothelium-derived relaxing factor in these vessels
Field Exercise on Frontier Issues in Africa: Sustainability Science in Action. A Final Research Report Submitted to the Graduate Program in Sustainability Science â Global Leadership Initiative (GPSS-GLI)
No abstract available
Field Exercise on Frontier Issues in Africa: Sustainability Science in Action. A Final Research Report Submitted to the Graduate Program in Sustainability Science â Global Leadership Initiative (GPSS-GLI)
No abstract available
Synthesis of calcitonin gene-related peptide (CGRP) by rat arterial endothelial cells
We investigated the protein and mRNA
expression of calcitonin gene-related peptide (CGRP) in
endothelial cells of the rat thoracic aorta and femoral
artery. Light microscopic immunocytochemistry
revealed that immunoreactivity for CG RP was
preferentially located in the endothelium of both vessels.
Immunoelectron microscopy showed that CGRPimmunoreactive gold particles were preferentially
localized on cisterns of the rough endoplasmic reticulum
and on the Weibel-Palade (WP) bodies in the endothelial
cells. Prepro CGRP mRNA signals were also detected
on the endothelium. Our results are the first to
demonstrate that endothelial cells of both elastic and
large muscular arteries synthesize CGRP and store it, in
part, in WP bodies, implying that CGRP may act as an
endothelium-derived relaxing factor in these vessels
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