705 research outputs found
Space shuttle navigation analysis
A detailed analysis of space shuttle navigation for each of the major mission phases is presented. A covariance analysis program for prelaunch IMU calibration and alignment for the orbital flight tests (OFT) is described, and a partial error budget is presented. The ascent, orbital operations and deorbit maneuver study considered GPS-aided inertial navigation in the Phase III GPS (1984+) time frame. The entry and landing study evaluated navigation performance for the OFT baseline system. Detailed error budgets and sensitivity analyses are provided for both the ascent and entry studies
Space shuttle navigation analysis. Volume 2: Baseline system navigation
Studies related to the baseline navigation system for the orbiter are presented. The baseline navigation system studies include a covariance analysis of the Inertial Measurement Unit calibration and alignment procedures, postflight IMU error recovery for the approach and landing phases, on-orbit calibration of IMU instrument biases, and a covariance analysis of entry and prelaunch navigation system performance
Towards spatiotemporal integration of bus transit with data-driven approaches
This study aims to propose an approach for spatiotemporal integration of bus
transit, which enables users to change bus lines by paying a single fare. This
could increase bus transit efficiency and, consequently, help to make this mode
of transportation more attractive. Usually, this strategy is allowed for a few
hours in a non-restricted area; thus, certain walking distance areas behave
like "virtual terminals." For that, two data-driven algorithms are proposed in
this work. First, a new algorithm for detecting itineraries based on bus GPS
data and the bus stop location. The proposed algorithm's results show that 90%
of the database detected valid itineraries by excluding invalid markings and
adding times at missing bus stops through temporal interpolation. Second, this
study proposes a bus stop clustering algorithm to define suitable areas for
these virtual terminals where it would be possible to make bus transfers
outside the physical terminals. Using real-world origin-destination trips, the
bus network, including clusters, can reduce traveled distances by up to 50%,
making twice as many connections on average.Comment: 20 pages, 16 FIGURE
T and CPT Symmetries in Entangled Neutral Meson Systems
Genuine tests of an asymmetry under T and/or CPT transformations imply the
interchange between in-states and out-states. I explain a methodology to
perform model-indepedent separate measurements of the three CP, T and CPT
symmetry violations for transitions involving the decay of the neutral meson
systems in B- and {\Phi}-factories. It makes use of the quantum-mechanical
entanglement only, for which the individual state of each neutral meson is not
defined before the decay of its orthogonal partner. The final proof of the
independence of the three asymmetries is that no other theoretical ingredient
is involved and that the event sample corresponding to each case is different
from the other two. The experimental analysis for the measurements of these
three asymmetries as function of the time interval {\Delta}t > 0 between the
first and second decays is discussed, as well as the significance of the
expected results. In particular, one may advance a first observation of true,
direct, evidence of Time-Reserval-Violation in B-factories by many standard
deviations from zero, without any reference to, and independent of,
CP-Violation. In some quantum gravity framework the CPT-transformation is
ill-defined, so there is a resulting loss of particle-antiparticle identity.
This mechanism induces a breaking of the EPR correlation in the entanglement
imposed by Bose statistics to the neutral meson system, the so-called
{\omega}-effect. I present results and prospects for the {\omega}-parameter in
the correlated neutral meson-antimeson states.Comment: Proc. DISCRETE 2010, Symposium on Prospects in the Physics of
Discrete Symmetries, December 2010, Rom
Quantum Fields on the Groenewold-Moyal Plane
We give an introductory review of quantum physics on the noncommutative
spacetime called the Groenewold-Moyal plane. Basic ideas like star products,
twisted statistics, second quantized fields and discrete symmetries are
discussed. We also outline some of the recent developments in these fields and
mention where one can search for experimental signals.Comment: 50 pages, 3 figures. v2: published versio
Cytosolic chaperones influence the fate of a toxin dislocated from the endoplasmic reticulum
The plant cytotoxin ricin enters target mammalian cells by receptor-mediated endocytosis and undergoes retrograde transport to the endoplasmic reticulum (ER). Here, its catalytic A chain (RTA) is reductively separated from the cell-binding B chain, and free RTA enters the cytosol where it inactivates ribosomes. Cytosolic entry requires unfolding of RTA and dislocation across the ER membrane such that it arrives in the cytosol in a vulnerable, nonnative conformation. Clearly, for such a dislocated toxin to become active, it must avoid degradation and fold to a catalytic conformation. Here, we show that, in vitro, Hsc70 prevents aggregation of heat-treated RTA, and that RTA catalytic activity is recovered after chaperone treatment. A combination of pharmacological inhibition and cochaperone expression reveals that, in vivo, cytosolic RTA is scrutinized sequentially by the Hsc70 and Hsp90 cytosolic chaperone machineries, and that its eventual fate is determined by the balance of activities of cochaperones that regulate Hsc70 and Hsp90 functions. Cytotoxic activity follows Hsc70-mediated escape of RTA from an otherwise destructive pathway facilitated by Hsp90. We demonstrate a role for cytosolic chaperones, proteins typically associated with folding nascent proteins, assembling multimolecular protein complexes and degrading cytosolic and stalled, cotranslocational clients, in a toxin triage, in which both toxin folding and degradation are initiated from chaperone-bound states
Normal tau polarisation as a sensitive probe of CP violation in chargino decay
CP violation in the spin-spin correlations in chargino production and
subsequent two-body decay into a tau and a tau-sneutrino is studied at the ILC.
From the normal polarisation of the tau, an asymmetry is defined to test the
CP-violating phase of the higgsino mass parameter \mu. Asymmetries of more than
\pm70% are obtained, also in scenarios with heavy first and second generation
sfermions. Bounds on the statistical significances of the CP asymmetries are
estimated. As a result, the normal tau polarisation in the chargino decay is
one of the most sensitive probes to constrain or measure the phase \phi_\mu at
the ILC, motivating further detailed experimental studies.Comment: 20 pages, 10 figures, gzipped tar fil
Cytosolic chaperones influence the fate of a toxin dislocated from the endoplasmic reticulum
The plant cytotoxin ricin enters target mammalian cells by receptor-mediated endocytosis and undergoes retrograde transport to the endoplasmic reticulum (ER). Here, its catalytic A chain (RTA) is reductively separated from the cell-binding B chain, and free RTA enters the cytosol where it inactivates ribosomes. Cytosolic entry requires unfolding of RTA and dislocation across the ER membrane such that it arrives in the cytosol in a vulnerable, nonnative conformation. Clearly, for such a dislocated toxin to become active, it must avoid degradation and fold to a catalytic conformation. Here, we show that, in vitro, Hsc70 prevents aggregation of heat-treated RTA, and that RTA catalytic activity is recovered after chaperone treatment. A combination of pharmacological inhibition and cochaperone expression reveals that, in vivo, cytosolic RTA is scrutinized sequentially by the Hsc70 and Hsp90 cytosolic chaperone machineries, and that its eventual fate is determined by the balance of activities of cochaperones that regulate Hsc70 and Hsp90 functions. Cytotoxic activity follows Hsc70-mediated escape of RTA from an otherwise destructive pathway facilitated by Hsp90. We demonstrate a role for cytosolic chaperones, proteins typically associated with folding nascent proteins, assembling multimolecular protein complexes and degrading cytosolic and stalled, cotranslocational clients, in a toxin triage, in which both toxin folding and degradation are initiated from chaperone-bound states
Sampling-based Algorithms for Optimal Motion Planning
During the last decade, sampling-based path planning algorithms, such as
Probabilistic RoadMaps (PRM) and Rapidly-exploring Random Trees (RRT), have
been shown to work well in practice and possess theoretical guarantees such as
probabilistic completeness. However, little effort has been devoted to the
formal analysis of the quality of the solution returned by such algorithms,
e.g., as a function of the number of samples. The purpose of this paper is to
fill this gap, by rigorously analyzing the asymptotic behavior of the cost of
the solution returned by stochastic sampling-based algorithms as the number of
samples increases. A number of negative results are provided, characterizing
existing algorithms, e.g., showing that, under mild technical conditions, the
cost of the solution returned by broadly used sampling-based algorithms
converges almost surely to a non-optimal value. The main contribution of the
paper is the introduction of new algorithms, namely, PRM* and RRT*, which are
provably asymptotically optimal, i.e., such that the cost of the returned
solution converges almost surely to the optimum. Moreover, it is shown that the
computational complexity of the new algorithms is within a constant factor of
that of their probabilistically complete (but not asymptotically optimal)
counterparts. The analysis in this paper hinges on novel connections between
stochastic sampling-based path planning algorithms and the theory of random
geometric graphs.Comment: 76 pages, 26 figures, to appear in International Journal of Robotics
Researc
First Production and Detection of Cold Antihydrogen Atoms
The ATHENA experiment recently produced the first atoms of cold antihydrogen.
This paper gives a brief review of how this was achieved.Comment: Invited talk at Int. Conf. on Low Energy Antiprotons 2003 (LEAP03),
to be published in NIM
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