Arizona v. Johnson: Determining When a Terry Stop Becomes Consensual

The study of crowding effects on particle diffusion is a large subject with implications in many scientific areas. The studies span from pure theoretical calculations to experiments actually measuring the movement of proteins diffusing in a cell. Even though the subject is important and has been studied heavily there are still aspects not fully understood.   This report describes a Monte Carlo simulation approach (Gillespie algorithm) to study the effects of crowding on particle diffusion in a quasi one-dimensional system. With quasi meaning that the particles diffuses on a one-dimensional lattice but has the possibility to disassociate from the lattice and then rebind at a latter stage. Different binding strategies are considered: rebinding to the same location and randomly choosing the binding location. The focus of the study is how these strategies affects the mobility (diffusion coefficient) of a tracer particle. The main result of this thesis is a graph showing the diffusion coefficient as a function of the binding rate for different binding strategies and particle densities. We provide analytical estimates for the diffusion coefficient in the unbinding rate limits which show good agreement with the simulations.Hur "trängsel" (från engelskans "crowding" t ex molecular crowding) påverkar diffusionsprocesser är viktigt inom många olika vetenskapliga områden. Forskningen som för tillfället utförs sträcker sig från rent teoretiska beräkningar till experiments där man kan följa enskilda proteiners rörelse i en cell. Även fast ämnet är viktig och väl undersökt finns det fortfarande många aspekter som man inte förstår till fullo. I det här examensarbetet beskrivs en Monte Carlo metod (Gillespie algoritmen) för att studera hur trängsel påverkar en partikel som diffunderar i ett "nästan" en-dimensonellt system. Det är nästan en-dimensionellt i det avsedde att partiklarna diffunderar på ett gitter men kan binda av från gittret och binda tillbaka i ett senare skedde. Olika metoder för hur partiklarna binder till gittret undersöks: Återbinding till avbindingsplatsen och slumpmässigt vald återbindingsplats. Fokus ligger på att förklara hur dessa påverkar mobiliteten (diffusionskonstanten) av en spårningspartikel (tracer particle). Resultatet är en graf som visar diffusionskonstanten för spårningspartikeln som en funktion av avbindingsfrekvens för olika bindingstrategier och partikeldensiteter. Vi ger också analytiska resultat i gränsvärdet för höga och låga avbindingstakter vilka stämmer bra överens med simuleringar

The Power of Posner: A Study of Prestige and Influence in the Federal Judiciary

Some judges have a disproportionate influence over the American judiciary; existing research has shown Judge Richard Posner is one of those judges. Our goal was to identify and determine how Judge Posner’s influence has changed over time. To measure and track his influence, we collected and compared citation and invocation data from three distinct time frames. While these measurements are imperfect, they can help illustrate the level of influence and prestige Judge Posner enjoys. The existing literature led us to expect Judge Posner’s early citation rates to be low. After several years on the bench, the citation rates for each opinion should rise dramatically. By contrast, Judge Posner’s citation rates are exceptionally high from the outset while more recent opinions actually have lower citation rates

Width is not additive

We develop a construction suggested by Scharlemann and Thompson to obtain an infinite family of pairs of knots $K_{\alpha}$ and $K'_{\alpha}$ so that w(K_{\alpha} # K'_{\alpha})=max{w(K_{\alpha}), w(K'_{\alpha})}. This is the first known example of a pair of knots such that w(K#K') and it establishes that the lower bound w(K#K')\geq max{w(K),w(K')} obtained by Scharlemann and Schultens is best possible. Furthermore, the knots $K_{\alpha}$ provide an example of knots where the number of critical points for the knot in thin position is greater than the number of critical points for the knot in bridge position.Comment: 48 pages, 25 figure

Using Delay-Differential Equations for Modeling Calcium Cycling in Cardiac Myocytes

The cycling of calcium at the intracellular level of cardiac cells plays a key role in the excitation-contraction process. The interplay between ionic currents, buffering agents, and calcium release from the sarcoplasmic reticulum (SR) is a complex system that has been shown experimentally to exhibit complex dynamics including period-2 states (alternans) and higher-order rhythms. Many of the calcium cycling activities involve the sensing, binding, or diffusion of calcium between intracellular compartments; these are physical processes that take time and typically are modeled by “relaxation” equations where the steady-state value and time course of a particular variable are specified through an ordinary differential equation (ODE) with a time constant. An alternative approach is to use delay-differential equations (DDEs), where the delays in the system correspond to non-instantaneous events. In this thesis, we present a thorough overview of results from calcium cycling experiments and proposed intracellular calcium cycling models, as well as the context of alternans and delay-differential equations in cardiac modeling. We utilize a DDE to model the diffusion of calcium through the SR by replacing the relaxation ODE typically used for this process. The relaxation time constant τa is replaced by a delay δj, which could also be interpreted as the refractoriness of ryanodine receptor channels after releasing calcium from the sarcoplasmic reticulum. This is the first application of delay-differential equations to modeling calcium cycling dynamics, and to modeling cardiac systems at the cellular level. We analyzed the dynamical behaviors of the system and focus on the factors that have been shown to produce alternans and irregular dynamics in experiments and models with cardiac myocytes. We found that chaotic calcium dynamics could occur even for a more physiologically revelant SR calcium release slope than comparable ODE models. Increasing the SR release slope did not affect the calcium dynamics, but only shifted behavior down to lower values of the delay, allowing alternans, higher-order behavior, and chaos to occur for smaller delays than in simulations with a normal SR release slope. For moderate values of the delay, solely alternans and 1:1 steady-state behavior were observed. Above a particular threshold value for the delay, chaos appeared in the dynamics and further increasing the delay caused the system to destabilize under broader ranges of periods. We also compare our results with other models of intracellular calcium cycling and suggest promising avenues for further development of our preliminary work

The Impact of Customer Collaboration on Agile Product Development Success in Technology Startups Within the Pacific Northwest

While agile software development is being adopted in more organizations recently, many products using the methodology are still failing in the market due to inadequate customer collaboration despite the purported benefits. Within start-ups, where speed and early market penetration can be the death or success of a company, understanding if using agile software development including adequate customer collaboration makes a significant difference is important. A study which investigates the impact of including customer collaboration in the agile product development process could uncover whether or not a product is successful within technology focused start-up’s in the Pacific Northwest. This research could allow technology focused start-ups to learn how to emulate success and avoid pitfalls using agile software development to create better, more transformative products for the world. The research question is: how does the inclusion of customer collaboration in the agile product development process by product owners impact the overall success of the product within Pacific Northwest technology start-up companies? This concept paper includes information on the nature of the study, the significance, relationship to cognate, a literature review beginning, and a significant amount of research related to the hypothesis