Adapting Appropriation Water Law to Accommodate Equitable Consideration of Instream Flow Uses

The increasing public interest in naturally flowing streams has fostered efforts to obtain their protection under existing state water laws. In this study, the water laws of Arizona, Colorado, Idaho, Montana, Nevada, New Mexico, Utah, and Wyoming were examined and compared 1) with each other, and 2) against a set of aleitn criteria, to assess shortcomings in accommodating instream flow protections. It was determined that the appropriation system has the essential features of and ambodies legal principles that should allow the accommodation of instream flow values but, at this time, purchase of existing rights or the exercise of governmental reservation/withdrawal/appropriation authorities seem to be the primary options. Legislative, judicial, and adminsitrative strategies for protecting instream flows apart from the normal appropriation process were reviewed. Certain legislative and administrative strategies hold premise as supplementary to the standard appropriation procedure. Likewise, private sector strategies utilizing contracts, easements, purchase of development rights, etc., need to be more thoroughly considered. Where instream flow protections do not justify preemptive rights and strategies, and if hydrologic imperatives are properly observed, the state administered appropriation systems can accommodate the instream flow needs. However, the need for better technical information for establishing benficial need for the many instream values, and for use in projecting the biologic-hydrologic consequences of particular instream flow regimes remains a stumbling block to the accommodation process

Adapting Water Services to Urban Growth: A Case Study of Salt Lake County

Urbanizing areas thorughout the nation are considering governmental reorganization or consolidation to coordinate planning and improve the cost effectiveness of the delivery of public services. More efficient water supply and wastewater services may become important in the political debate over reorganization. However water factors figure politically, accomplished reorganizations must carefully plan for efficent provision of water services. This study profiles the structure and interactions of municipalities and water service agencies in Utah\u27s Salt Lake County during the 1970s. Both 1975 and 1978 attempts to consolidate Salt Lake City and the unincorporated areas of the county failed. The voting patterns, interest ground positions, and issues are examined. One major water issue surfaced in a concern that service jurisdictions and financial obligations were not sufficiently defined to protect the communities previously bound through water service agreements but excluded from the consolidated government. Additionally, the proposed dissolution of the County Water Conservancy District raised doubts on the division of equity in water rights and distribution facilities. Any large water development stabilizes institutional arrangements to a degree which may become a financial and legal contrainst to desired change. Overall, nonwater issues dominated the decision in this water sensitive area. This implies that water service jurisdictional alignments are set by political decisions based on nonwater considerations. Water utilities must do their best to be effective in the resulting context

On a initial value problem arising in mechanics

We study initial value problem for a system consisting of an integer order and distributed-order fractional differential equation describing forced oscillations of a body attached to a free end of a light viscoelastic rod. Explicit form of a solution for a class of linear viscoelastic solids is given in terms of a convolution integral. Restrictions on storage and loss moduli following from the Second Law of Thermodynamics play the crucial role in establishing the form of the solution. Some previous results are shown to be special cases of the present analysis

Diffusion in multiscale spacetimes

We study diffusion processes in anomalous spacetimes regarded as models of quantum geometry. Several types of diffusion equation and their solutions are presented and the associated stochastic processes are identified. These results are partly based on the literature in probability and percolation theory but their physical interpretation here is different since they apply to quantum spacetime itself. The case of multiscale (in particular, multifractal) spacetimes is then considered through a number of examples and the most general spectral-dimension profile of multifractional spaces is constructed.Comment: 23 pages, 5 figures. v2: discussion improved, typos corrected, references adde

Retarding Sub- and Accelerating Super-Diffusion Governed by Distributed Order Fractional Diffusion Equations

We propose diffusion-like equations with time and space fractional derivatives of the distributed order for the kinetic description of anomalous diffusion and relaxation phenomena, whose diffusion exponent varies with time and which, correspondingly, can not be viewed as self-affine random processes possessing a unique Hurst exponent. We prove the positivity of the solutions of the proposed equations and establish the relation to the Continuous Time Random Walk theory. We show that the distributed order time fractional diffusion equation describes the sub-diffusion random process which is subordinated to the Wiener process and whose diffusion exponent diminishes in time (retarding sub-diffusion) leading to superslow diffusion, for which the square displacement grows logarithmically in time. We also demonstrate that the distributed order space fractional diffusion equation describes super-diffusion phenomena when the diffusion exponent grows in time (accelerating super-diffusion).Comment: 11 pages, LaTe

The origin of large molecules in primordial autocatalytic reaction networks

Large molecules such as proteins and nucleic acids are crucial for life, yet their primordial origin remains a major puzzle. The production of large molecules, as we know it today, requires good catalysts, and the only good catalysts we know that can accomplish this task consist of large molecules. Thus the origin of large molecules is a chicken and egg problem in chemistry. Here we present a mechanism, based on autocatalytic sets (ACSs), that is a possible solution to this problem. We discuss a mathematical model describing the population dynamics of molecules in a stylized but prebiotically plausible chemistry. Large molecules can be produced in this chemistry by the coalescing of smaller ones, with the smallest molecules, the `food set', being buffered. Some of the reactions can be catalyzed by molecules within the chemistry with varying catalytic strengths. Normally the concentrations of large molecules in such a scenario are very small, diminishing exponentially with their size. ACSs, if present in the catalytic network, can focus the resources of the system into a sparse set of molecules. ACSs can produce a bistability in the population dynamics and, in particular, steady states wherein the ACS molecules dominate the population. However to reach these steady states from initial conditions that contain only the food set typically requires very large catalytic strengths, growing exponentially with the size of the catalyst molecule. We present a solution to this problem by studying `nested ACSs', a structure in which a small ACS is connected to a larger one and reinforces it. We show that when the network contains a cascade of nested ACSs with the catalytic strengths of molecules increasing gradually with their size (e.g., as a power law), a sparse subset of molecules including some very large molecules can come to dominate the system.Comment: 49 pages, 17 figures including supporting informatio

Infrared spectroscopy of phytochrome and model pigments

Fourier-transform infrared difference spectra between the red-absorbing and far-red-absorbing forms of oat phytochrome have been measured in H2O and 2H2O. The difference spectra are compared with infrared spectra of model compounds, i.e. the (5Z,10Z,15Z)- and (5Z,10Z,15E)-isomers of 2,3,7,8,12,13,17,18-octaethyl-bilindion (Et8-bilindion), 2,3-dihydro-2,3,7,8,12,13,17,18-octaethyl-bilindion (H2Et8-bilindion), and protonated H2Et8-bilindion in various solvents. The spectra of the model compounds show that only for the protonated forms can clear differences between the two isomers be detected. Since considerable differences are present between the spectra of Et8-bilindion and H2Et8-bilindion, it is concluded that only the latter compound can serve as a model system of phytochrome. The 2H2O effect on the difference spectrum of phytochrome supports the view that the chromophore in red-absorbing phytochrome is protonated and suggests, in addition, that it is also protonated in far-red-absorbing phytochrome. The spectra show that protonated carboxyl groups are influenced. The small amplitudes in the difference spectra exclude major changes of protein secondary structure

Mass coupling and Q−1ofimpurity−limitednormalQ^{-1} of impurity-limited normal ^3$He in a torsion pendulum

We present results of the $Q^{-1}$ and period shift, $\Delta P$, for $^3$He confined in a 98% nominal open aerogel on a torsion pendulum. The aerogel is compressed uniaxially by 10% along a direction aligned to the torsion pendulum axis and was grown within a 400 $\mu$m tall pancake (after compression) similar to an Andronikashvili geometry. The result is a high $Q$ pendulum able to resolve $Q^{-1}$ and mass coupling of the impurity-limited $^3$He over the whole temperature range. After measuring the empty cell background, we filled the cell above the critical point and observe a temperature dependent period shift, $\Delta P$, between 100 mK and 3 mK that is 2.9$$ of the period shift (after filling) at 100 mK. The $Q^{-1}$ due to the $^3$He decreases by an order of magnitude between 100 mK and 3 mK at a pressure of $0.14\pm0.03$ bar. We compare the observable quantities to the corresponding calculated $Q^{-1}$ and period shift for bulk $^3$He.Comment: 8 pages, 3 figure