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Vol 31, Part I - forums.sou.edu • Index page - Southern Oregon ...

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ABSTRACTS – Contributed Oral Papers<br />

temperatures were summarized to identify the first and last<br />

days of a 1500 growing-degree-day growing season. Precipitation<br />

was accumulated from the end of the growing season<br />

the previous year through <strong>31</strong> December, 1 January through<br />

the beginning of the current year growing season, and during<br />

the current growing season. These weather records were then<br />

subjected to principal components analysis. The eight years<br />

characterizing extremes in each of the five principal components<br />

were identified. Extreme year effects on calf growth<br />

were contrasted for each principal component. Irrespective<br />

of the pattern of precipitation before the growing season and<br />

with near or above average precipitation during the growing<br />

season, calves reared in years characterized by longer,<br />

cooler growing seasons gained more weight from birth to<br />

weaning than those reared in opposing years. This retrospective<br />

analysis indicates a general increase in temperature in<br />

the Northern Great Plains is expected to r<strong>edu</strong>ce the growth<br />

of calves from birth to weaning.<br />

MATHEMATICS<br />

Monday, starting at 10:30 a.m. in PONDEROSA PINES 1 & 2<br />

123 Perfect Stripes from a General Turing Model in Different<br />

Geometries, JEAN SCHNEIDER (Department of<br />

Mathematics, Boise State University, 1910 University Drive,<br />

Boise, ID 83725; jeanschneider@u.boisestate.<strong>edu</strong>).<br />

We explore a striped pattern generated by a general<br />

Turing model in three different geometries. We look at the<br />

square, disk, and hemisphere and make connections between<br />

the stripes in each spatial direction. In particular, we gain a<br />

greater understanding of when perfect stripes can be generated<br />

and what causes defects in their patterns. In this investigation<br />

we look at the difference between the solutions due<br />

to the different domain shapes. In the end we lay out a reason<br />

why stripes from a reaction-diffusion system can be perfect<br />

on a square or hemisphere, but can never be perfect on a disk.<br />

124 Markov Chains on the Symmetric Groups Converging to<br />

Non-uniform Measures, YUNJIANG JIANG (Department<br />

of Mathematics, Stanford University, building 380, Stanford,<br />

California 94305; yunjiangster@gmail.com).<br />

The study of random walks on finite groups, and in<br />

particular symmetric groups, viewed as card-shuffling models,<br />

has seen tremendous activities in recent decades. An<br />

extremely challenging set of problems concerns the mixing<br />

time in total variation as well as other distances on the space<br />

of probability measures. These problems have many practical<br />

consequences ranging from the effectiveness of Monte-<br />

Carlo simulation to number of times one needs to shuffle a<br />

deck of cards to mix it properly. Here we introduce several<br />

other important measures on the symmetric groups other<br />

than the uniform, construct natural Markov chains converging<br />

to them, and analyze their mixing times in sharp form<br />

84<br />

via results from symmetric function theory. We also introduce<br />

more general families of measures given by class functions,<br />

and analyze the associated Metropolis chains using<br />

the so-called path method. In particular we give a small<br />

degree polynomial bound for the uniform sampling chain on<br />

derangements, based on the random transposition walk. We<br />

will also mention a few open problems towards the end.<br />

125 Nondefective Secant Varieties of Split Varieties, DOUG-<br />

LAS A TORRANCE (Department of Mathematics, University<br />

of Idaho, 300 Brink Hall, Moscow, ID 83844; torrance@<br />

vandals.uidaho.<strong>edu</strong>).<br />

Suppose R is the polynomial ring in n+1 variables with<br />

coefficients in an algebraically closed field of characteristic<br />

zero k. The set of all homogeneous polynomials in R of<br />

degree d can be considered as a vector space over k. By considering<br />

two nonzero polynomials to be equivalent if they<br />

are scalar multiples of each other, we can define a projective<br />

space. The split variety, or variety of completely decomposable<br />

forms, consists of all points in this projective space<br />

which correspond to polynomials that are the product of d<br />

linear factors.<br />

For every s distinct points lying on this variety, there<br />

is an (s-1)-plane containing them. We define the closure of<br />

the union of all these (s-1)-planes as the secant variety. We<br />

expect that the secant variety of a split variety will either fill<br />

up the projective space or have dimension s(dn+1). In this<br />

case, the secant variety is said to be nondefective. Otherwise,<br />

it is said to be defective.<br />

It is conjectured that the secant variety to a split variety<br />

will be defective if and only if d = 2 and 2 ≤ s ≤ n/2. It<br />

remains to show that the remaining cases are nondefective.<br />

In this talk, we discuss new results in this area.<br />

Mathematics oral presentations continue on Tuesday.<br />

Please refer to <strong>page</strong> 90 in these Proceedings.<br />

CELL and MOLECULAR BIOLOGY<br />

Tuesday, starting at 8:40 a.m. in WILLOWS 2<br />

126 A Role for Inflammatory Cytokines in Breast Cancer<br />

Cell EMT, HUNTER COVERT*, NICOLE ANKEN-<br />

BRANDT, RANDY RYAN, and CHERYL JORCYK<br />

(Department of Biological Sciences, Boise State University,<br />

1910 University Drive, Boise, ID 83725; Huntercovert@u.<br />

boisestate.<strong>edu</strong>).<br />

Inflammatory cytokines are expressed in high levels during<br />

breast tumor development. Tumor cells, as well as monocytes,<br />

macrophages, and neutrophils, secrete these cytokines.<br />

Our preliminary results have shown certain inflammatory<br />

cytokines cause an increase in cell detachment as well<br />

as a change in morphology. The change in cell morphology<br />

can be studied by looking at cellular markers which are<br />

expressed when a cell displays an epithelial or mesenchymal

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