113 research outputs found
Enhanced heat transport by turbulent two-phase Rayleigh-B\'enard convection
We report measurements of turbulent heat-transport in samples of ethane
(CH) heated from below while the applied temperature difference straddled the liquid-vapor co-existance curve . When the sample
top temperature decreased below , droplet condensation occurred
and the latent heat of vaporization provided an additional heat-transport
mechanism.The effective conductivity increased linearly with
decreasing , and reached a maximum value that was an
order of magnitude larger than the single-phase . As
approached the critical pressure, increased dramatically even
though vanished. We attribute this phenomenon to an enhanced
droplet-nucleation rate as the critical point is approached.Comment: 4 gages, 6 figure
Non-Oberbeck-Boussinesq effects in turbulent thermal convection in ethane close to the critical point
As shown in earlier work (Ahlers et al., J. Fluid Mech. 569, p.409 (2006)),
non-Oberbeck Boussinesq (NOB) corrections to the center temperature in
turbulent Rayleigh-Benard convection in water and also in glycerol are governed
by the temperature dependences of the kinematic viscosity and the thermal
diffusion coefficient. If the working fluid is ethane close to the critical
point the origin of non-Oberbeck-Boussinesq corrections is very different, as
will be shown in the present paper. Namely, the main origin of NOB corrections
then lies in the strong temperature dependence of the isobaric thermal
expansion coefficient \beta(T). More precisely, it is the nonlinear
T-dependence of the density \rho(T) in the buoyancy force which causes another
type of NOB effect. We demonstrate that through a combination of experimental,
numerical, and theoretical work, the latter in the framework of the extended
Prandtl-Blasius boundary layer theory developed in Ahlers et al., J. Fluid
Mech. 569, p.409 (2006). The latter comes to its limits, if the temperature
dependence of the thermal expension coefficient \beta(T) is significant.Comment: 18 pages, 15 figures, 3 table
Heat transport by turbulent Rayleigh-B\'enard convection for $\Pra\ \simeq 0.83\times 10^{12} \alt \Ra\ \alt 10^{15}\Gamma = 0.50$
We report experimental results for heat-transport measurements, in the form
of the Nusselt number \Nu, by turbulent Rayleigh-B\'enard convection in a
cylindrical sample of aspect ratio ( m is
the diameter and m the height). The measurements were made using
sulfur hexafluoride at pressures up to 19 bars as the fluid. They are for the
Rayleigh-number range 3\times 10^{12} \alt \Ra \alt 10^{15} and for Prandtl
numbers \Pra\ between 0.79 and 0.86. For \Ra < \Ra^*_1 \simeq 1.4\times
10^{13} we find \Nu = N_0 \Ra^{\gamma_{eff}} with , consistent with classical turbulent Rayleigh-B\'enard convection in a
system with laminar boundary layers below the top and above the bottom plate.
For \Ra^*_1 < \Ra < \Ra^*_2 (with \Ra^*_2 \simeq 5\times 10^{14})
gradually increases up to . We argue that above
\Ra^*_2 the system is in the ultimate state of convection where the boundary
layers, both thermal and kinetic, are also turbulent. Several previous
measurements for are re-examined and compared with the present
results.Comment: 44 pages, 18 figures, submitted to NJ
Large scale dynamics in turbulent Rayleigh-Benard convection
The progress in our understanding of several aspects of turbulent
Rayleigh-Benard convection is reviewed. The focus is on the question of how the
Nusselt number and the Reynolds number depend on the Rayleigh number Ra and the
Prandtl number Pr, and on how the thicknesses of the thermal and the kinetic
boundary layers scale with Ra and Pr. Non-Oberbeck-Boussinesq effects and the
dynamics of the large-scale convection-roll are addressed as well. The review
ends with a list of challenges for future research on the turbulent
Rayleigh-Benard system.Comment: Review article, 34 pages, 13 figures, Rev. Mod. Phys. 81, in press
(2009
Oligodendrocytes Do Not Export NAA-Derived Aspartate In Vitro.
Oligodendroglial cells are known to de-acetylate the N-acetylaspartate (NAA) synthesized and released by neurons and use it for lipid synthesis. However, the role of NAA regarding their intermediary metabolism remains poorly understood. Two hypotheses were proposed regarding the fate of aspartate after being released by de-acetylation: (1) aspartate is metabolized in the mitochondria of oligodendrocyte lineage cells; (2) aspartate is released to the medium. We report here that aspartoacylase mRNA expression increases when primary rat oligodendrocyte progenitor cells (OPCs) differentiate into mature cells in culture. Moreover, characterising metabolic functions of acetyl coenzyme A and aspartate from NAA catabolism in mature oligodendrocyte cultures after 5 days using isotope-labelled glucose after 5-days of differentiation we found evidence of extensive NAA metabolism. Incubation with [1,6-13C]glucose followed by gas chromatography-mass spectrometry and high performance liquid chromatography analyses of cell extracts and media in the presence and absence of NAA established that the acetate moiety produced by hydrolysis of NAA does not enter mitochondrial metabolism in the form of acetyl coenzyme A. We also resolved the controversy concerning the possible release of aspartate to the medium: aspartate is not released to the medium by oligodendrocytes in amounts detectable by our methods. Therefore we propose that: aspartate released from NAA joins the cytosolic aspartate pool rapidly and takes part in the malate-aspartate shuttle, which transports reducing equivalents from glycolysis into the mitochondria for ATP production and enters the tricarboxylic acid cycle at a slow rate.This work was supported by grants from the
UK Multiple Sclerosis Society and from Qatar Foundation. The
work was further supported by core funding from the Wellcome
Trust and MRC to the Wellcome Trust-Medical Research Council
Cambridge Stem Cell Institute. The authors acknowledge the excellent
technical support in GC-MS and HPLC analysis from Lars Evje
(NTNU, Norway).This is the final version of the article. It first appeared from Springer at http://dx.doi.org/10.1007/s11064-016-1985-y
The CCR4-NOT Complex Physically and Functionally Interacts with TRAMP and the Nuclear Exosome
BACKGROUND: Ccr4-Not is a highly conserved multi-protein complex consisting in yeast of 9 subunits, including Not5 and the major yeast deadenylase Ccr4. It has been connected functionally in the nucleus to transcription by RNA polymerase II and in the cytoplasm to mRNA degradation. However, there has been no evidence so far that this complex is important for RNA degradation in the nucleus. METHODOLOGY/PRINCIPAL FINDINGS: In this work we point to a new role for the Ccr4-Not complex in nuclear RNA metabolism. We determine the importance of the Ccr4-Not complex for the levels of non-coding nuclear RNAs, such as mis-processed and polyadenylated snoRNAs, whose turnover depends upon the nuclear exosome and TRAMP. Consistently, mutation of both the Ccr4-Not complex and the nuclear exosome results in synthetic slow growth phenotypes. We demonstrate physical interactions between the Ccr4-Not complex and the exosome. First, Not5 co-purifies with the exosome. Second, several exosome subunits co-purify with the Ccr4-Not complex. Third, the Ccr4-Not complex is important for the integrity of large exosome-containing complexes. Finally, we reveal a connection between the Ccr4-Not complex and TRAMP through the association of the Mtr4 helicase with the Ccr4-Not complex and the importance of specific subunits of Ccr4-Not for the association of Mtr4 with the nuclear exosome subunit Rrp6. CONCLUSIONS/SIGNIFICANCE: We propose a model in which the Ccr4-Not complex may provide a platform contributing to dynamic interactions between the nuclear exosome and its co-factor TRAMP. Our findings connect for the first time the different players involved in nuclear and cytoplasmic RNA degradation
- …