Utilization and Maintenance in a Model with Terminal Scrapping

We draw on three strands of literature dealing with utilization, maintenance, and scrapping in order to analyze the properties of the respective policies and their interac-tions. We do so by focusing on the last period of the received multi-period service life model and extending it in three directions: first, by associating the physical deteriora-tion of equipment to the intensity of its utilization and maintenance; second, by ex-panding on the range of explainable operating policies to allow for idling, mothballing, capacity depleting, capacity preserving, full capacity, upgrading, and downgrading; and, third, by linking the operating policies to the capital policy of scrapping. Owing to these enhancements, the analysis leads to several important findings. One among them is that optimal operating policies behave usually in opposite directions, proceed-ing in time from harder to softer or vice versa, depending on the net revenue earning capability of the equipment under consideration. Another is that profit (loss) making equipment is scrappable iff on the average the operating capital deteriorates faster (slower), or equivalently improves slower (faster), than the scrapping capital. And still an-other result is that operating policies are determined jointly with scrapping policy capi-tal policies, thus suggesting that empirical investigations of their determinants should allow for this simultaneityUtilization, maintenance, idling, mothballing, capacity depleting, capacity pre-serving, upgrading, downgrading, scrapping

Operating policies in a model with terminal scrapping

We draw on three strands of literature dealing with utilization, maintenance, and scrapping in order to analyze the properties of the respective policies and their interac-tions. We do so by focusing on the last period of the received multi-period service life model and extending it in three directions: first, by associating the physical deteriora-tion of equipment to the intensity of its utilization and maintenance; second, by ex-panding on the range of explainable operating policies to allow for idling, mothballing, capacity depleting, capacity preserving, full capacity, upgrading, and downgrading; and, third, by linking the operating policies to the capital policy of scrapping. Owing to these enhancements, the analysis leads to several important findings. One among them is that optimal operating policies behave usually in opposite directions, proceed-ing in time from harder to softer or vice versa, depending on the net revenue earning capability of the equipment under consideration. Another is that profit (loss) making equipment is scrappable iff on the average the operating capital deteriorates faster (slower), or equivalently improves slower (faster), than the scrapping capital. And still an-other result is that operating policies are determined jointly with scrapping policy capi-tal policies, thus suggesting that empirical investigations of their determinants should allow for this simultaneity.Utilization, maintenance, idling, mothballing, capacity depleting, capacity pre-serving, upgrading, downgrading, scrapping.

A Rehabilitation of Economic Replacement Theory

Our objective in this paper is to shed light on the economic forces and the specific way in which they combine to determine the service life, and hence the replacement demand for durables, in the short run and in the long run. For this purpose the received multiperiod economic replacement model is extended in the light of more recent theoretical developments and solved for the number and duration of replacements. Owing mainly to the intuition that the latter decisions are inexplicably related to the owner s profit horizon, aside from steady state replacement, the model is shown to yield a range of transitional and limiting replacement policies that have been largely ignored in the literature. In addition, the results indicate that : a) the optimal service life is consistently determined by such conventional forces of short-term variation as utilization, maintenance, operating safety, interest rate, uncertainty due to technological breakthroughs, the price of new and used durables, etc., b) switching among replacement policies produces bursts or slumps in replacement investment much like the spikes discovered recently at the plant level, and c) in non- stationary economic environments the error from applying steady state replacement, instead of the more appropriate transitory replacement policies reported in this paper, may be substantial.service life, replacement, and scrapping

Embryonic and post-embryonic utilization and subcellular localization of the nuclear receptor SpSHR2 in the sea urchin

SpSHR2 (Strongylocentrotus purpuratus steroid hormone receptor 2) is a nuclear receptor, encoded by a maternal RNA in the sea urchin embryo. These maternal SpSHR2 transcripts, which are present in all cells, persist until the blastula stage and then are rapidly turned over. A small fraction of the embryonic SpSHR2 protein is maternal, but the majority of this nuclear receptor in the embryo is the product of new synthesis, presumably from the maternal RNA after fertilization. In agreement with the mRNA distribution, the SpSHR2 protein is also detected in all embryonic cells. Contrary to the RNA though, the SpSHR2 protein persists throughout embryonic development to the pluteus stage, long after the mRNA is depleted. Following fertilization and as soon as the 2-cell stage, the cytoplasmic SpSHR2 protein enters rapidly into the embryonic nuclei where it appears in the form of speckles. During subsequent stages (from fourth cleavage onward), SpSHR2 resides in speckled form in both the nucleus and the cytoplasm of the embryonic cells. The cytoplasmic localization of SpSHR2 differs between polarized and non-polarized cells, maintaining an apical position in the ectoderm and endoderm versus a uniform distribution in mesenchyme cells. Following the end of embryonic development (pluteus stage), the SpSHR2 protein is depleted from all tissues. During the ensuing four weeks of larval development, the SpSHR2 is not detected in either the larval or the rudiment cells which will give rise to the adult. Just prior to metamorphosis, at about 35 days post-fertilization, the protein is detected again but in contrast to the uniform distribution in the early embryo, the larval SpSHR2 is specifically expressed in cells of the mouth epithelium and the epaulettes. In adult ovaries and testes, SpSHR2 is specifically detected in the myoepithelial cells surrounding the ovarioles and the testicular acini. Nuclear SpSHR2 in blastula extracts binds to the C1R hormone response element in the upstream promoter region of the CyIIIb actin gene indicating that the latter may be a target of this nuclear receptor in the sea urchin embryo

Nonlinear optics of III-V semiconductors in the terahertz regime: an ab-initio study

We compute from first principles the infrared dispersion of the nonlinear susceptibility $\chi^{(2)}$ in zincblende semiconductors. At terahertz frequencies the nonlinear susceptibility depends not only on the purely electronic response $\chi^{(2)}_{\infty}$, but also on three other parameters $C_1$, $C_2$ and $C_3$ describing the contributions from ionic motion. They relate to the TO Raman polarizability, the second-order displacement-induced dielectric polarization, and the third-order lattice potential. Contrary to previous theory, we find that mechanical anharmonicity ($C_3$) dominates over electrical anharmonicity ($C_2$), which is consistent with recent experiments on GaAs. We predict that the sharp minimum in the intensity of second-harmonic generation recently observed for GaAs between $\omega_{\rm TO}/2$ and $\omega_{\rm TO}$ does not occur for several other III-V compounds.Comment: 9 pages, 3 figures; updated bibliograph

The Transmission Property of the Discrete Heisenberg Ferromagnetic Spin Chain

We present a mechanism for displaying the transmission property of the discrete Heisenberg ferromagnetic spin chain (DHF) via a geometric approach. By the aid of a discrete nonlinear Schr\"odinger-like equation which is the discrete gauge equivalent to the DHF, we show that the determination of transmitting coefficients in the transmission problem is always bistable. Thus a definite algorithm and general stochastic algorithms are presented. A new invariant periodic phenomenon of the non-transmitting behavior for the DHF, with a large probability, is revealed by an adoption of various stochastic algorithms.Comment: 16 pages, 7 figure

The sociology of an allocative structure: Housing: In what ways do studies of the housing market in command economies modify our view of ecological processes?

[Δε διατίθεται περίληψη / no abstract available][Δε διατίθεται περίληψη / no abstract available

From Single-Cell to Whole-Body: Developing a Molecular Neuroscience Toolkit

Throughout my Ph.D. I have worked on technology development, at first to answer basic scientific questions and eventually for therapeutic applications. This technology development applied to a variety of fields, from neuroscience to development to gene therapy, and acted upon biological systems in a wide range of scale, from the single-cell monitoring to organism-wide gene-transfer. My graduate research began with the engineering of microbial rhodopsin spectral properties and fluorescence. By making use of their ability to absorb light and emit fluorescence in a voltage-dependent manner, I aimed to interrogate neuronal activity during behavior at the single-cell level. That line of research ended with publication of the voltage-sensor Archer, which I used to track activity of a single cell in vivo in awake, behaving worms. I then shifted from tracking activity at the single cell level, to visualizing entire organisms, by developing clearing techniques that enable a high-resolution, three-dimensional analysis of a diverse range of tissues. I began by optimizing tissue-clearing parameters for various tissue types and a wide variety of experimental needs. I then took that knowledge and applied it to visualizing and tracking the developing neural crest in cleared, whole-mount chicken embryos, discovering some unexpected derivates. Finally, I became interested not only in visualizing entire organisms, but in developing technologies to facilitate gene transfer throughout the body. The rapidly growing field of gene therapy is in constant need of new tools that target specific tissues, avoiding off-target effects. The end of my Ph.D. has been spent engineering viruses that can be delivered body-wide, but target only specific areas of therapeutic interest, like the brain and lungs.</p

Influence of the passive region on Zero Field Steps for window Josephson junctions

We present a numerical and analytic study of the influence of the passive region on fluxon dynamics in a window junction. We examine the effect of the extension of the passive region and its electromagnetic characteristics, its surface inductance and capacitance. When the velocity in the passive region $v_{I}$ is equal to the Swihart velocity (1) a one dimensional model describes well the operation of the device. When $v_{I}$ is different from 1, the fluxon adapts its velocity to $v_{I}$. In both cases we give simple formulas for the position of the limiting voltage of the zero field steps. Large values of inductance and capacitance lead to different types of solutions which are analyzed.Comment: 12 pages, 13 figure

Exact Kink Solitons in the Presence of Diffusion, Dispersion, and Polynomial Nonlinearity

We describe exact kink soliton solutions to nonlinear partial differential equations in the generic form u_{t} + P(u) u_{x} + \nu u_{xx} + \delta u_{xxx} = A(u), with polynomial functions P(u) and A(u) of u=u(x,t), whose generality allows the identification with a number of relevant equations in physics. We emphasize the study of chirality of the solutions, and its relation with diffusion, dispersion, and nonlinear effects, as well as its dependence on the parity of the polynomials $P(u)$ and $A(u)$ with respect to the discrete symmetry $u\to-u$. We analyze two types of kink soliton solutions, which are also solutions to 1+1 dimensional phi^{4} and phi^{6} field theories.Comment: 11 pages, Late