NASA ESTO Lidar Technologies Investment Strategy: 2016 Decadal Update

The NASA Earth Science Technology Office (ESTO) recently updated its investment strategy in the area of lidar technologies as it pertains to NASA's Earth Science measurement goals in the next decade. The last ESTO lidar strategy was documented in 2006. The current (2016) report assesses the state-of-the-art in lidar technologies a decade later. Lidar technology maturation in the past decade has been evaluated, and the ESTO investment strategy is updated and laid out in this report according to current NASA Earth science measurement needs and new emerging technologies

2016 Decadal Update of the NASA ESTO Lidar Technologies Investment Strategy

We describe the 2016 update of the NASA Earth Science Technology Office (ESTO) investment strategy in the area of lidar technologies as pertaining to NASAs Earth Science measurement goals in the next decade

On Quantum Entropy and Excess Entropy Production in a System-Environment Pure State

We explore a recently introduced quantum thermodynamic entropy $S^Q_{univ}$ of a pure state of a composite system-environment computational "universe" with a simple system $\mathcal{S}$ coupled to a constant temperature bath $\mathcal{E}$. The principal focus is "excess entropy production" in which the quantum entropy change is greater than expected from the classical entropy-free energy relationship. We analyze this in terms of quantum spreading of time dependent states, and its interplay with the idea of a microcanonical shell. The entropy takes a basis-dependent Shannon information definition. We argue for the zero-order $\mathcal{SE}$ energy basis as the unique choice that gives classical thermodynamic relations in the limit of weak coupling and high density of states, including an exact division into system and environment components. Entropy production takes place due to two kinds of processes. The first is classical "ergodization" that fills the full density of states within the microcanonical shell. The second is excess entropy production related to quantum spreading or "quantum ergodization" of the wavepacket that effectively increases the width of the energy shell. Lorentzian superpositions with finite microcanonical shell width lead to classical results as the limiting case, with no excess entropy. We then consider a single $\mathcal{SE}$ zero-order initial state, as the examplar of extreme excess entropy production. Systematic formal results are obtained for a unified treatment of excess entropy production for time-dependent Lorentzian superpositions, and verified computationally. It is speculated that the idea of free energy might be extended to a notion of "available energy" corresponding to the excess entropy production. A unified perspective on quantum thermodynamic entropy is thereby attained from the classical limit to extreme quantum conditions.Comment: 24+21 pages (double spaced), 6+6 figure

Differential sensitivity of TREK-1, TREK-2 and TRAAK background potassium channels to the polycationic dye ruthenium red

BACKGROUND AND PURPOSE: Pharmacological separation of the background potassium currents of closely related K2P channels is a challenging problem. We previously demonstrated that ruthenium red (RR) inhibits TASK-3 (K2 P 9.1), but not TASK-1 (K2 P 3.1) channels. RR has been extensively used to distinguish between TASK currents in native cells. In the present study, we systematically investigate the RR sensitivity of a more comprehensive set of K2 P channels. EXPERIMENTAL APPROACH: K+ currents were measured by two-electrode voltage clamp in Xenopus oocytes and by whole-cell patch clamp in mouse dorsal root ganglion (DRG) neurons. KEY RESULTS: RR differentiates between two closely related members of the TREK subfamily. TREK-2 (K2 P 10.1) proved to be highly sensitive to RR (IC50 = 0.2 muM), whereas TREK-1 (K2 P 2.1) was not affected by the compound. We identified aspartate 135 (D135) as the target of the inhibitor in mouse TREK-2c. D135 lines the wall of the extracellular ion pathway (EIP), a tunnel structure through the extracellular cap characteristic for K2 P channels. TREK-1 contains isoleucine in the corresponding position. The mutation of this isoleucine (I110D) rendered TREK-1 sensitive to RR. The third member of the TREK subfamily, TRAAK (K2 P 4.1) was more potently inhibited by ruthenium violet, a contaminant in some RR preparations, than by RR. DRG neurons predominantly express TREK-2 and RR-resistant TREK-1 and TRESK (K2 P 18.1) background K+ channels. We detected the RR-sensitive leak K+ current component in DRG neurons. CONCLUSIONS AND IMPLICATIONS: We propose that RR may be useful for distinguishing TREK-2 (K2P 10.1) from TREK-1 (K2P 2.1) and other RR-resistant K2 P channels in native cells

The LQLP Calcineurin-docking Site Is a Major Determinant of the Calcium-dependent Activation of Human TRESK Background K+ Channel

Calcium-dependent activation of human TRESK (TWIK-related spinal cord K+ channel, K2P18.1) depends on direct targeting of calcineurin to the PQIIIS motif. In the present study we demonstrate that TRESK also contains another functionally relevant docking site for the phosphatase, the LQLP amino acid sequence. Combined mutations of the PQIIIS and LQLP motifs were required to eliminate the calcium-dependent regulation of the channel. In contrast to the alanine substitutions of PQIIIS, the mutation of LQLP to AQAP alone did not significantly change the amplitude of TRESK activation evoked by the substantial elevation of cytoplasmic calcium concentration. However, the AQAP mutation slowed down the response to high calcium. In addition, modest elevation of [Ca2+], which effectively regulated the wild type channel, failed to activate TRESK-AQAP. This indicates that the AQAP mutation diminished the sensitivity of TRESK to calcium. Even if PQIIIS was replaced by the PVIVIT sequence of high calcineurin-binding affinity, the effect of the AQAP mutation was clearly detected in this TRESK-PVIVIT context. Substitution of the LQLP region with the corresponding fragment of NFAT transcription factor, perfectly matching the previously described LxVP calcineurin-binding consensus sequence, increased the calcium-sensitivity of TRESK-PVIVIT. Thus the enhancement of the affinity of TRESK for calcineurin by the incorporation of PVIVIT could not compensate for or prevent the effects of LQLP sequence modifications, suggesting that the two calcineurin-binding regions play distinct roles in the regulation. Our results indicate that the LQLP site is a fundamental determinant of the calcium-sensitivity of human TRESK

Numerical analysis of oscillating flow about a circular cylinder

The numerical experiments, carried out through the use of the vorticity­ stream function equations and their finite difference form, on sinusoidally­ oscillating as well as co-existing flows (sinusoidal oscillation plus steady mean flow) at low and intermediate Keulegan-Carpenter numbers are described. A third-order in time, second-order in space, three-level predictor-corrector finite­ difference scheme has been used. The Poisson equation for the stream function was solved by a Fast Poisson Solver based on the High Order Difference Approximation with Identity Expansion (HODIE) and the Fast Fourier Transform (FFT) methods provided by the National Center for Atmospheric Research for the solution of separable elliptic partial differential equations with a non-square grid. The analysis has produced force-transfer and fluid-damping coefficients comparable to those obtained experimentally for both types of flows (i.e., with and without current) and to those obtained with a square grid through the use of the IMSL library.http://archive.org/details/numericalanalysi00lotsLieutenant Commander, United States NavyApproved for public release; distribution is unlimited

Promise of Graph Sparsification and Decomposition for Noise Reduction in QAOA: Analysis for Trapped-Ion Compilations

We develop new approximate compilation schemes that significantly reduce the expense of compiling the Quantum Approximate Optimization Algorithm (QAOA) for solving the Max-Cut problem. Our main focus is on compilation with trapped-ion simulators using Pauli-$X$ operations and all-to-all Ising Hamiltonian $H_\text{Ising}$ evolution generated by Molmer-Sorensen or optical dipole force interactions, though some of our results also apply to standard gate-based compilations. Our results are based on principles of graph sparsification and decomposition; the former reduces the number of edges in a graph while maintaining its cut structure, while the latter breaks a weighted graph into a small number of unweighted graphs. Though these techniques have been used as heuristics in various hybrid quantum algorithms, there have been no guarantees on their performance, to the best of our knowledge. This work provides the first provable guarantees using sparsification and decomposition to improve quantum noise resilience and reduce quantum circuit complexity. For quantum hardware that uses edge-by-edge QAOA compilations, sparsification leads to a direct reduction in circuit complexity. For trapped-ion quantum simulators implementing all-to-all $H_\text{Ising}$ pulses, we show that for a $(1-\epsilon)$ factor loss in the Max-Cut approximation ($\epsilon>0)$, our compilations improve the (worst-case) number of $H_\text{Ising}$ pulses from $O(n^2)$ to $O(n\log(n/\epsilon))$ and the (worst-case) number of Pauli-$X$ bit flips from $O(n^2)$ to $O\left(\frac{n\log(n/\epsilon)}{\epsilon^2}\right)$ for $n$-node graphs. We demonstrate significant reductions in noise are obtained in our new compilation approaches using theory and numerical calculations for trapped-ion hardware. We anticipate these approximate compilation techniques will be useful tools in a variety of future quantum computing experiments