3,461 research outputs found

    Is there excess co-movement of primary commodity prices? A co-integration test

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    It is a common perception that primary commodity prices tend to move together. This perception is especially common among commodity traders who may justify an increase in the price of one commodity because the prices of other commodities have increased. This commodity price co-movement can be identified among commodities that seem unrelated in terms of production or consumption substitutability or complementarity. But there is no reason for believing that prices of unrelated commodities should move together, except for macroeconomic shocks affecting commodity markets in general. For example, in a recession commodity prices decline across the board because demand declines; and in periods of generalinflation commodity prices rise, partly because commodities provide a hedge against inflation. However, after accounting for macroeconomic shocks, is co-movement among prices still evident? In this paper, the authors test for co-movement and excess co-movement of primary commodity prices using the econometric tests of co-integration in time series and the resulting error-correction models (ECM). The ECMs will be used to examine the existence of short-run excess co-movement between commodity prices, taking into consideration the long-run relationship between them.Crops&Crop Management Systems,Environmental Economics&Policies,Montreal Protocol,Markets and Market Access,Access to Markets

    Review of Cipriani Alessandro, and Giri Maurizio 'Electronic Music and Sound Design: Theory and Practice with Max/MSP'.

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    A book review of Cipriani and Giri's "Electronic Music and Sound Design: Theory and Practice with Max/MSP, Volume 1"

    High-speed seal and bearing test facility

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    The following topics are discussed in this viewgraph presentation: high speed seal/bearing rig background, project status, facility features, test rig capabilities, EMD testing advantages, and future opportunities

    Towards trainable synthesis for optimized circuit deployment on FPGA

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    Field Programmable Gate Arrays (FPGAs) utilize multiple programmable elements and non-programmable blocks. After synthesizing an input Hardware Design Language (HDL) design into a circuit, optimizations are used to discover a satisfactory deployment on a target FPGA. HDLs' compound operations, such as addition, can be implemented in various ways and thus, multiple but functionally equivalent circuits can be synthesized. To leverage this, we propose a methodology that first enables configurable synthesis of compound operations. Second, it trains the system using a set of HDL files and architectures to optimize target performance objectives, such as critical path length and power. We prototyped our technique in the open source Verilog-To-Routing (VTR) tool. We subsequently produced two configuration files targeting different deployment objectives; experimental results with the VTR Verilog benchmarks revealed significant improvements

    The Complexity of Separating Points in the Plane

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    We study the following separation problem: given n connected curves and two points s and t in the plane, compute the minimum number of curves one needs to retain so that any path connecting s to t intersects some of the retained curves. We give the first polynomial (O(n3)) time algorithm for the problem, assuming that the curves have reasonable computational properties. The algorithm is based on considering the intersection graph of the curves, defining an appropriate family of closed walks in the intersection graph that satisfies the 3-path-condition, and arguing that a shortest cycle in the family gives an optimal solution. The 3-path-condition has been used mainly in topological graph theory, and thus its use here makes the connection to topology clear. We also show that the generalized version, where several input points are to be separated, is NP-hard for natural families of curves, like segments in two directions or unit circles

    Universal trend of the information entropy of a fermion in a mean field

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    We calculate the information entropy of single-particle states in position-space SrS_{r} and momentum-space SkS_{k} for a nucleon in a nucleus, a Λ\Lambda particle in a hypernucleus and an electron in an atomic cluster. It is seen that SrS_{r} and SkS_{k} obey the same approximate functional form as functions of the number of particles, SrS_{r} ({\rm or} Sk)=a+bN1/3S_{k}) = a+bN^{1/3} in all of the above many-body systems in position- and momentum- space separately. The net information content Sr+SkS_{r}+S_{k} is a slowly varying function of NN of the same form as above. The entropy sum Sr+SkS_{r}+S_{k} is invariant to uniform scaling of coordinates and a characteristic of the single-particle states of a specific system. The order of single-particle states according to Sr+SkS_r +S_k is the same as their classification according to energy keeping the quantum number nn constant. The spin-orbit splitting is reproduced correctly. It is also seen that Sr+SkS_{r}+S_{k} enhances with excitation of a fermion in a quantum-mechanical system. Finally, we establish a relationship of Sr+SkS_r +S_k with the energy of the corresponding single-particle state i.e. Sr+Sk=kln(μE+ν)S_r +S_k = k \ln (\mu E +\nu). This relation holds for all the systems under consideration.Comment: 9 pages, latex, 6 figure

    Surface Transformations and Water Uptake on Liquid and Solid Butanol near the Melting Temperature

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    Water interactions with organic surfaces are of central importance in biological systems and many Earth system processes. Here we describe experimental studies of water collisions and uptake kinetics on liquid and solid butanol from 160 to 200 K. Hyperthermal D2O molecules (0.32 eV) undergo efficient trapping on both solid and liquid butanol, and only a minor fraction scatters inelastically after an 80% loss of kinetic energy to surface modes. Trapped molecules either desorb within a few ms, or are taken up by the butanol phase during longer times. The water uptake and surface residence time increase with temperature above 180 K indicating melting of the butanol surface 4.5 K below the bulk melting temperature. Water uptake changes gradually across the melting point and trapped molecules are rapidly lost by diffusion into the liquid above 190 K. This indicates that liquid butanol maintains a surface phase with limited water permeability up to 5.5 K above the melting point. These surface observations are indicative of an incremental change from solid to liquid butanol over a range of 10 K straddling the bulk melting temperature, in contrast to the behavior of bulk butanol and previously studied materials.Comment: 28 pages, 4 figures + introduction figur
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