1,974 research outputs found
Measurement of the current-phase relation of superconducting atomic contacts
We have probed the current-phase relation of an atomic contact placed with a
tunnel junction in a small superconducting loop. The measurements are in
quantitative agreement with the predictions of a resistively shunted SQUID
model in which the Josephson coupling of the contact is calculated using the
independently determined transmissions of its conduction channels.Comment: to be published in Physical Review Letter
Estimating the number of change-points in a two-dimensional segmentation model without penalization
In computational biology, numerous recent studies have been dedicated to the
analysis of the chromatin structure within the cell by two-dimensional
segmentation methods. Motivated by this application, we consider the problem of
retrieving the diagonal blocks in a matrix of observations. The theoretical
properties of the least-squares estimators of both the boundaries and the
number of blocks proposed by L\'evy-Leduc et al. [2014] are investigated. More
precisely, the contribution of the paper is to establish the consistency of
these estimators. A surprising consequence of our results is that, contrary to
the onedimensional case, a penalty is not needed for retrieving the true number
of diagonal blocks. Finally, the results are illustrated on synthetic data.Comment: 30 pages, 8 figure
Non-degenerate, three-wave mixing with the Josephson ring modulator
The Josephson ring modulator (JRM) is a device, based on Josephson tunnel
junctions, capable of performing non-degenerate mixing in the microwave regime
without losses. The generic scattering matrix of the device is calculated by
solving coupled quantum Langevin equations. Its form shows that the device can
achieve quantum-limited noise performance both as an amplifier and a mixer.
Fundamental limitations on simultaneous optimization of performance metrics
like gain, bandwidth and dynamic range (including the effect of pump depletion)
are discussed. We also present three possible integrations of the JRM as the
active medium in a different electromagnetic environment. The resulting
circuits, named Josephson parametric converters (JPC), are discussed in detail,
and experimental data on their dynamic range are found to be in good agreement
with theoretical predictions. We also discuss future prospects and requisite
optimization of JPC as a preamplifier for qubit readout applications.Comment: 21 pages, 16 figures, 4 table
The Spitzer c2d Survey of Nearby Dense Cores. IX. Discovery of a Very Low Luminosity Object Driving a Molecular Outflow in the Dense Core L673-7
We present new infrared, submillimeter, and millimeter observations of the
dense core L673-7 and report the discovery of a low-luminosity, embedded Class
0 protostar driving a molecular outflow. L673-7 is seen in absorption against
the mid-infrared background in 5.8, 8, and 24 micron Spitzer images, allowing
for a derivation of the column density profile and total enclosed mass of
L673-7, independent of dust temperature assumptions. Estimates of the core mass
from these absorption profiles range from 0.2-4.5 solar masses. Millimeter
continuum emission indicates a mass of about 2 solar masses, both from a direct
calculation assuming isothermal dust and from dust radiative transfer models
constrained by the millimeter observations. We use dust radiative transfer
models to constrain the internal luminosity of L673-7, defined to be the
luminosity of the central source and excluding the luminosity from external
heating, to be 0.01-0.045 solar luminosities, with 0.04 solar luminosities the
most likely value. L673-7 is thus classified as a very low luminosity object
(VeLLO), and is among the lowest luminosity VeLLOs yet studied. We calculate
the kinematic and dynamic properties of the molecular outflow in the standard
manner, and we show that the expected accretion luminosity based on these
outflow properties is greater than or equal to 0.36 solar luminosities. The
discrepancy between this expected accretion luminosity and the internal
luminosity derived from dust radiative transfer models indicates that the
current accretion rate is much lower than the average rate over the lifetime of
the outflow. Although the protostar embedded within L673-7 is consistent with
currently being substellar, it is unlikely to remain as such given the
substantial mass reservoir remaining in the core.Comment: 19 pages, 14 figures. Accepted by Ap
Ergodicity of the statistic and purity of neutron resonance data
The statistic characterizes the fluctuations of the number of
levels as a function of the length of the spectral interval. It is studied as a
possible tool to indicate the regular or chaotic nature of underlying dynamics,
detect missing levels and the mixing of sequences of levels of different
symmetry, particularly in neutron resonance data. The relation between the
ensemble average and the average over different fragments of a given
realization of spectra is considered. A useful expression for the variance of
which accounts for finite sample size is discussed. An analysis
of neutron resonance data presents the results consistent with a maximum
likelihood method applied to the level spacing distribution.Comment: 24 pages, 19 figures, 1 tabl
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The Spitzer c2d Survey Of Nearby Dense Cores. X. Star Formation In L673 And Cb188
L673 and CB188 are two low-mass clouds isolated from large star-forming regions that were observed as part of the Spitzer Legacy Project "From Molecular Clouds to Planet Forming disks" (c2d). We identified and characterized all the young stellar objects (YSOs) of these two regions and modeled their spectral energy distributions (SEDs) to examine whether their physical properties are consistent with values predicted from the theoretical models and with the YSO properties in the c2d survey of larger clouds. Overall, 30 YSO candidates were identified by the c2d photometric criteria, 27 in L673 and 3 in CB188. We confirm the YSO nature of 29 of them and remove a false Class III candidate in L673. We further present the discovery of two new YSO candidates, one Class 0 and another possible Class I candidate in L673, therefore bringing the total number of YSO candidates to 31. Multiple sites of star formation are present within L673, closely resembling other well-studied c2d clouds containing small groups such as B59 and L1251B, whereas CB188 seems to consist of only one isolated globule-like core. We measure a star formation efficiency (SFE) of 4.6%, which resembles the SFE of the larger c2d clouds. From the SED modeling of our YSO sample we obtain envelope masses for Class I and Flat spectrum sources of 0.01-1.0 M-circle dot. The majority of Class II YSOs show disk accretion rates from 3.3 x 10(-10) to 3 x 10(-8) M-circle dot yr(-1) and disk masses that peak at 10(-4) to 10(-3) M-circle dot. Finally, we examined the possibility of thermal fragmentation in L673 as the main star-forming process. We find that the mean density of the regions where significant YSO clustering occurs is of the order of similar to 10(5) cm(-3) using 850 mu m observations and measure a Jeans Length that is greater than the near-neighbor YSO separations by approximately a factor of 3-4. We therefore suggest that other processes, such as turbulence and shock waves, may have had a significant effect on the cloud's filamentary structure and YSO clustering.University of SouthamptonNASA 1279198, 1288806, 1365763Jet Propulsion Laboratory, California Institute of TechnologyAstronom
Notch signaling is associated with ALDH activity and an aggressive metastatic phenotype in murine osteosarcoma cells
Osteosarcoma (OS) is the most common primary malignancy of bone, and pulmonary metastatic disease accounts for nearly all mortality. However, little is known about the biochemical signaling alterations that drive the progression of metastatic disease. Two murine OS cell populations, K7M2 and K12, are clonally related but differ significantly in their metastatic phenotypes and therefore represent excellent tools for studying metastatic OS molecular biology. K7M2 cells are highly metastatic, whereas K12 cells display limited metastatic potential. Here we report that the expression of Notch genes (Notch1, 2, 4) are up-regulated, including downstream targets Hes1 and Stat3, in the highly metastatic K7M2 cells compared to the less metastatic K12 cells, indicating that the Notch signaling pathway is more active in K7M2 cells. We have previously described that K7M2 cells exhibit higher levels of aldehyde dehydrogenase (ALDH) activity. Here we report that K7M2 cell ALDH activity is reduced with Notch inhibition, suggesting that ALDH activity may be regulated in part by the Notch pathway. Notch signaling is also associated with increased resistance to oxidative stress, migration, invasion, and VEGF expression in vitro. However, Notch inhibition did not significantly alter K7M2 cell proliferation. In conclusion, we provide evidence that Notch signaling is associated with ALDH activity and increased metastatic behavior in OS cells. Both Notch and ALDH are putative molecular targets for the treatment and prevention of OS metastasis. © 2013 Mu, Isaac, Greco, Huard and Weiss
Rapamycin inhibits ALDH activity, resistance to oxidative stress, and metastatic potential in murine osteosarcoma cells
Osteosarcoma (OS) is the most common primary malignancy of bone. Mortality is determined by the presence of metastatic disease, but little is known regarding the biochemical events that drive metastases. Two murine OS cell lines, K7M2 and K12, are related but differ significantly in their metastatic potentials: K7M2 is highly metastatic whereas K12 displays much less metastatic potential. Using this experimental system, the mammalian target of rapamycin (mTOR) pathway has been implicated in OS metastasis. We also discovered that aldehyde dehydrogenase (ALDH, a stem cell marker) activity is higher in K7M2 cells than K12 cells. Rapamycin treatment reduces the expression and enzymatic activity of ALDH in K7M2 cells. ALDH inhibition renders these cells more susceptible to apoptotic death when exposed to oxidative stress. Furthermore, rapamycin treatment reduces bone morphogenetic protein-2 (BMP2) and vascular endothelial growth factor (VEGF) gene expression and inhibits K7M2 proliferation, migration, and invasion in vitro. Inhibition of ALDH with disulfiram correlated with decreased mTOR expression and activity. In conclusion, we provide evidence for interaction between mTOR activity, ALDH activity, and metastatic potential in murine OS cells. Our work suggests that mTOR and ALDH are therapeutic targets for the treatment and prevention of OS metastasis. © 2013 Xiaodong Mu et al
Rapamycin inhibits ALDH activity, resistance to oxidative stress, and metastatic potential in murine osteosarcoma cells
Osteosarcoma (OS) is the most common primary malignancy of bone. Mortality is determined by the presence of metastatic disease, but little is known regarding the biochemical events that drive metastases. Two murine OS cell lines, K7M2 and K12, are related but differ significantly in their metastatic potentials: K7M2 is highly metastatic whereas K12 displays much less metastatic potential. Using this experimental system, the mammalian target of rapamycin (mTOR) pathway has been implicated in OS metastasis. We also discovered that aldehyde dehydrogenase (ALDH, a stem cell marker) activity is higher in K7M2 cells than K12 cells. Rapamycin treatment reduces the expression and enzymatic activity of ALDH in K7M2 cells. ALDH inhibition renders these cells more susceptible to apoptotic death when exposed to oxidative stress. Furthermore, rapamycin treatment reduces bone morphogenetic protein-2 (BMP2) and vascular endothelial growth factor (VEGF) gene expression and inhibits K7M2 proliferation, migration, and invasion in vitro. Inhibition of ALDH with disulfiram correlated with decreased mTOR expression and activity. In conclusion, we provide evidence for interaction between mTOR activity, ALDH activity, and metastatic potential in murine OS cells. Our work suggests that mTOR and ALDH are therapeutic targets for the treatment and prevention of OS metastasis. © 2013 Xiaodong Mu et al
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