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Comparing Sight-Resight Methods for Dog Populations: Analysis of 2015 and 2016 Rabies Vaccination Campaign Data from HaitiCleaton, Julie M 12 May 2017 (has links)
INTRODUCTION: Sight-resight studies are performed to estimate population sizes, in this case dog populations in rabies endemic areas.
AIM: This study compares one- and two-day sight-resight methods with two-day as the standard to explore the feasibility and accuracy of the one-day method in different vaccination campaign strategies and dog population characteristics.
METHODS: 2015 household survey data and sight-resight data are analyzed to find the percentage of free roaming and confined dogs in the community and use those to adjust the population estimate formulas. 2016 sight-resight data are analyzed as a two-day campaign and as if it had been a one-day campaign. In a sensitivity analysis, confidence intervals are explored in relation to vaccination coverage.
RESULTS: Before missed mark and proportion free-roaming corrections, the one-day method results in slightly underestimated population estimates to the two-day method when the vaccination campaign is central point, overestimated when door-to-door, and far underestimated when capture, vaccinate, release. After corrections door-to-door estimates were accurate whereas central point and capture, vaccinate, release estimates substantially underestimated population sizes.
DISCUSSION: Results suggest that the one-day mark-resight method could be used to conserve resources depending on the vaccination method and estimated coverage.
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Matrix correspondences and the enumeration of plane partitions.Gansner, Emden Robert January 1978 (has links)
Thesis. 1978. Ph.D.--Massachusetts Institute of Technology. Dept. of Mathematics. / MICROFICHE COPY AVAILABLE IN ARCHIVES AND SCIENCE. / Vita. / Bibliography: p. 213-217. / Ph.D.
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SYMMETRIC PRESENTATIONS AND CONSTRUCTIONSGomez, David R, Jr 01 June 2014 (has links)
In this thesis we have investigated permutation and monomial progenitors of the form p^*n:N (p=2,3,5,...) and p^*n:_m N (p=3,5,7,...) respectively. We have discovered new symmetric presentations of several finite nonabelian simple groups including linear groups, unitary groups, orthogonal groups, and sporadic groups. We have constructed interesting groups found using the technique of double coset enumeration and found the isomorphic types of the numerous groups that appeared as homorphic images. These include the sympletic group, S_4(5) and the Janko groups, J_2 and J_1 which were found using a variety of different control groups over finite fields.
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Cyclic Sieving Phenomenon of Promotion on Rectangular TableauxRhee, Donguk January 2012 (has links)
Cyclic sieving phenomenon (CSP) is a generalization by Reiner, Stanton, White of Stembridge's q=-1 phenomenon. When CSP is exhibited, orbits of a cyclic action on combinatorial objects show a nice structure and their sizes can be encoded by one polynomial.
In this thesis we study various proofs of a very interesting cyclic sieving phenomenon, that jeu-de-taquin promotion on rectangular Young tableaux exhibits CSP. The first proof was obtained by Rhoades, who used Kazhdan-Lusztig representation. Purbhoo's proof uses Wronski map to equate tableaux with points in the fibre of the map. Finally, we consider Petersen, Pylyavskyy, Rhoades's proof on 2 and 3 row tableaux by bijecting the promotion of tableaux to rotation of webs.
This thesis also propose a combinatorial approach to prove the CSP for square tableaux. A variation of jeu-de-taquin move yields a way to count square tableaux which has minimal orbit under promotion. These tableaux are then in bijection to permutations. We consider how this can be generalized.
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Effect of bacterial stress response on pathogen enumeration and its implications for food safetyWang, Huaiyu Unknown Date
No description available.
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Cyclic Sieving Phenomenon of Promotion on Rectangular TableauxRhee, Donguk January 2012 (has links)
Cyclic sieving phenomenon (CSP) is a generalization by Reiner, Stanton, White of Stembridge's q=-1 phenomenon. When CSP is exhibited, orbits of a cyclic action on combinatorial objects show a nice structure and their sizes can be encoded by one polynomial.
In this thesis we study various proofs of a very interesting cyclic sieving phenomenon, that jeu-de-taquin promotion on rectangular Young tableaux exhibits CSP. The first proof was obtained by Rhoades, who used Kazhdan-Lusztig representation. Purbhoo's proof uses Wronski map to equate tableaux with points in the fibre of the map. Finally, we consider Petersen, Pylyavskyy, Rhoades's proof on 2 and 3 row tableaux by bijecting the promotion of tableaux to rotation of webs.
This thesis also propose a combinatorial approach to prove the CSP for square tableaux. A variation of jeu-de-taquin move yields a way to count square tableaux which has minimal orbit under promotion. These tableaux are then in bijection to permutations. We consider how this can be generalized.
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Effect of bacterial stress response on pathogen enumeration and its implications for food safetyWang, Huaiyu 06 1900 (has links)
To determine the impact of stress response on enumeration, cell association status and the viability of Escherichia coli DH5, Staphylococcus aureus ATCC 13565 and Listeria monocytogenes CDC 7762 were evaluated using fluorescence microscopy and were compared with the outcomes of traditional plate count and optical density measurements. Fluorescence microscopy revealed that organic acid stress (acetic and lactic, pH 2.7-3.3) induced cell clumping with little loss of viability in Escherichia coli DH5. Significantly lower values for cell enumeration were found for plate counts and OD600 measurement, likely due to cell clumping in response to organic acid stress. Gram-negative bacteria Escherichia coli DH5 showed higher levels of clumping and subsequent resistance against organic acid stress. Increased cell surface hydrophobicity was found in cells that exhibited more evident clumping. However, inorganic acid stress (hydrochloric and sulfuric, pH 3.0-3.3) induced only very low level of clumping in stationary-phase Escherichia coli DH5 and almost no clumping in other cultures. Osmotic stress, heat and cold shock were not found to induce cell clumping. It has been determined that traditional enumeration methods have significantly underestimated the number of viable bacterial cells when organic acid stress is involved. Plate counts and OD600 measurement therefore need to be reassessed as tools for accurate evaluation of pathogens in food industry. / Food Science and Technology
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Accurate enumeration and identification of Testacea (Protozoa, Rhizopoda) in forest soil using scanning electron microscopyAoki, Yoshiyuki January 2003 (has links)
No description available.
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ALGORITHM FOR ENUMERATING HYPERGRAPH TRANSVERSALSCasita, Roscoe 10 April 2018 (has links)
This paper introduces the hypergraph transversal problem along with thefollowing iterative solutions: naive, branch and bound, and dynamic exponentialtime (NC-D). Odometers are introduced along with the functions that manipulatethem. The traditional definitions of hyperedge, hypergraph, etc., are redefined interms of odometers and lists. All algorithms and functions necessary to implementthe solution are presented along with techniques to validate and test the results.Lastly, parallelization advanced applications, and future research directions areexamined.
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Toward the Enumeration of Maximal Chains in the Tamari LatticesJanuary 2016 (has links)
abstract: The Tamari lattices have been intensely studied since they first appeared in Dov Tamari’s thesis around 1952. He defined the n-th Tamari lattice T(n) on bracketings of a set of n+1 objects, with a cover relation based on the associativity rule in one direction. Despite their interesting aspects and the attention they have received, a formula for the number of maximal chains in the Tamari lattices is still unknown. The purpose of this thesis is to convey my results on progress toward the solution of this problem and to discuss future work.
A few years ago, Bergeron and Préville-Ratelle generalized the Tamari lattices to the m-Tamari lattices. The original Tamari lattices T(n) are the case m=1. I establish a bijection between maximum length chains in the m-Tamari lattices and standard m-shifted Young tableaux. Using Thrall’s formula, I thus derive the formula for the number of maximum length chains in T(n).
For each i greater or equal to -1 and for all n greater or equal to 1, I define C(i,n) to be the set of maximal chains of length n+i in T(n). I establish several properties of maximal chains (treated as tableaux) and identify a particularly special property: each maximal chain may or may not possess a plus-full-set. I show, surprisingly, that for all n greater or equal to 2i+4, each member of C(i,n) contains a plus-full-set. Utilizing this fact and a collection of maps, I obtain a recursion for the number of elements in C(i,n) and an explicit formula based on predetermined initial values. The formula is a polynomial in n of degree 3i+3. For example, the number of maximal chains of length n in T(n) is n choose 3.
I discuss current work and future plans involving certain equivalence classes of maximal chains in the Tamari lattices. If a maximal chain may be obtained from another by swapping a pair of consecutive edges with another pair in the Hasse diagram, the two maximal chains are said to differ by a square move. Two maximal chains are said to be in the same equivalence class if one may be obtained from the other by making a set of square moves. / Dissertation/Thesis / Doctoral Dissertation Mathematics 2016
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