14 research outputs found

    Some Variations on Maxwell's Equations

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    In the first sections of this article, we discuss two variations on Maxwell's equations that have been introduced in earlier work--a class of nonlinear Maxwell theories with well-defined Galilean limits (and correspondingly generalized Yang-Mills equations), and a linear modification motivated by the coupling of the electromagnetic potential with a certain nonlinear Schroedinger equation. In the final section, revisiting an old idea of Lorentz, we write Maxwell's equations for a theory in which the electrostatic force of repulsion between like charges differs fundamentally in magnitude from the electrostatic force of attraction between unlike charges. We elaborate on Lorentz' description by means of electric and magnetic field strengths, whose governing equations separate into two fully relativistic Maxwell systems--one describing ordinary electromagnetism, and the other describing a universally attractive or repulsive long-range force. If such a force cannot be ruled out {\it a priori} by known physical principles, its magnitude should be determined or bounded experimentally. Were it to exist, interesting possibilities go beyond Lorentz' early conjecture of a relation to (Newtonian) gravity.Comment: 26 pages, submitted to a volume in preparation to honor Gerard Emch v. 2: discussion revised, factors of 4\pi corrected in some equation

    A taxonomic bibliography of the South American snakes of the Crotalus durissus complex (Serpentes, Viperidae)

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    Structure II gas hydrates found below the bottom-simulating reflector

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    Gas hydrates are a major component in the organic carbon cycle. Their stability is controlled by temperature, pressure, water chemistry, and gas composition. The bottom-simulating reflector (BSR) is the primary seismic indicator of the base of hydrate stability in continental margins. Here we use seismic, well log, and core data from the convergent margin offshore NW Borneo to demonstrate that the BSR does not always represent the base of hydrate stability and can instead approximate the boundary between structure I hydrates above and structure II hydrates below. At this location, gas hydrate saturation below the BSR is higher than above and a process of chemical fractionation of the migrating free gas is responsible for the structure I-II transition. This research shows that in geological settings dominated by thermogenic gas migration, the hydrate stability zone may extend much deeper than suggested by the BSR
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