173,862 research outputs found
The Editor\u27s Song
The program of the 2011 Mathfest\u27s opening banquet was MAA-The Musical!\u27 Produced by Annalisa Crannell and starring the MAA Players (active MAA members all), it highlighted activities of the Association and of Mathfest itself. This song represents the journals. It was sung by past editor Frank Farris to the tune of A Wand\u27ring Minstrel I, from Gilbert and Sullivan\u27s the Mikado
Variable Side-Look Angle Concept For Radar Mapping
Radar mapping of planets can be accomplished at lower cost and with reduced emphasis on propulsion system capability from spacecraft operating in elliptical orbit than from circular orbit
Words That Didn\u27t Make It
The following words are not in the dictionary, at least in the sense expected. The clues are how such words would be defined if they had made it to Webster\u27s
Universal expressions of population change by the Price equation: natural selection, information, and maximum entropy production
The Price equation shows the unity between the fundamental expressions of
change in biology, in information and entropy descriptions of populations, and
in aspects of thermodynamics. The Price equation partitions the change in the
average value of a metric between two populations. A population may be composed
of organisms or particles or any members of a set to which we can assign
probabilities. A metric may be biological fitness or physical energy or the
output of an arbitrarily complicated function that assigns quantitative values
to members of the population. The first part of the Price equation describes
how directly applied forces change the probabilities assigned to members of the
population when holding constant the metrical values of the members---a fixed
metrical frame of reference. The second part describes how the metrical values
change, altering the metrical frame of reference. In canonical examples, the
direct forces balance the changing metrical frame of reference, leaving the
average or total metrical values unchanged. In biology, relative reproductive
success (fitness) remains invariant as a simple consequence of the conservation
of total probability. In physics, systems often conserve total energy.
Nonconservative metrics can be described by starting with conserved metrics,
and then studying how coordinate transformations between conserved and
nonconserved metrics alter the geometry of the dynamics and the aggregate
values of populations. From this abstract perspective, key results from
different subjects appear more simply as universal geometric principles for the
dynamics of populations subject to the constraints of particular conserved
quantitiesComment: v2: Complete rewrite, new title and abstract. Changed focus to Price
equation as basis for universal expression of changes in populations. v3:
Cleaned up usage of terms virtual and reversible displacements and virtual
work and usage of d'Alembert's principle. v4: minor editing and correction
Simple unity among the fundamental equations of science
The Price equation describes the change in populations. Change concerns some
value, such as biological fitness, information or physical work. The Price
equation reveals universal aspects for the nature of change, independently of
the meaning ascribed to values. By understanding those universal aspects, we
can see more clearly why fundamental mathematical results in different
disciplines often share a common form. We can also interpret more clearly the
meaning of key results within each discipline. For example, the mathematics of
natural selection in biology has a form closely related to information theory
and physical entropy. Does that mean that natural selection is about
information or entropy? Or do natural selection, information and entropy arise
as interpretations of a common underlying abstraction? The Price equation
suggests the latter. The Price equation achieves its abstract generality by
partitioning change into two terms. The first term naturally associates with
the direct forces that cause change. The second term naturally associates with
the changing frame of reference. In the Price equation's canonical form, total
change remains zero because the conservation of total probability requires that
all probabilities invariantly sum to one. Much of the shared common form for
the mathematics of different disciplines may arise from that seemingly trivial
invariance of total probability, which leads to the partitioning of total
change into equal and opposite components of the direct forces and the changing
frame of reference.Comment: arXiv admin note: text overlap with arXiv:1810.0926
Natural selection. III. Selection versus transmission and the levels of selection
George Williams defined an evolutionary unit as hereditary information for
which the selection bias between competing units dominates the informational
decay caused by imperfect transmission. In this article, I extend Williams'
approach to show that the ratio of selection bias to transmission bias provides
a unifying framework for diverse biological problems. Specific examples include
Haldane and Lande's mutation-selection balance, Eigen's error threshold and
quasispecies, Van Valen's clade selection, Price's multilevel formulation of
group selection, Szathmary and Demeter's evolutionary origin of primitive
cells, Levin and Bull's short-sighted evolution of HIV virulence, Frank's
timescale analysis of microbial metabolism, and Maynard Smith and Szathmary's
major transitions in evolution. The insights from these diverse applications
lead to a deeper understanding of kin selection, group selection, multilevel
evolutionary analysis, and the philosophical problems of evolutionary units and
individuality
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