The fixed sample (best-of-n) search strategy and the sequential search (fixed threshold) strategy are two prominent models of search behavior. The sequential search strategy dominates the former strategy-yields an equal or CP-690550 cost higher expected net fitness return to searchers-when search costs are nontrivial and the distribution of quality among prospective mates is uniform or truncated normal. In this paper our objective is to determine
whether there are any search costs or distributions of male quality for which the sequential search strategy is inferior to the fixed sample search strategy. The two search strategies are derived under general conditions in which females evaluate encountered males by inspection of an indicator character that has some functional relationship to male quality. The Solutions are identical to the original models when the inspected male attribute is itself male quality. The sequential search strategy is shown TH-302 clinical trial to dominate the fixed sample search strategy for all search costs and distributions of male quality. Low search costs have been implicated to explain empirical observations
that are consistent with the use of a fixed sample search strategy, but under conditions in which the original models were derived there is no search cost or distribution of male quality that favors the fixed sample search strategy. Plausible alternative explanations for the apparent use of this search
strategy are discussed. (C) 2009 Elsevier Ltd. All rights reserved.”
“Mathematical models and clinical observations have demonstrated that microenvironmental hypoxia and acidosis are important selection factors during the later stages of the somatic evolution of breast cancer. The consequent promotion of constitutive upregulation of glycolysis and resistance to acid-induced cellular toxicity is hypothesized to be critical for the ability of cancer cells to invade host tissue. In this work we developed a 3D fixed lattice cellular automata model to study the role of these two phenotypes in determining morphology and the potential for invasion of ductal carcinoma in situ (DICIS), which in this work is defined as the erosion of a healthy epithelial cell layer and direct contact Docetaxel molecular weight with the basement membrane. The model was conceived as a 40-cell wide epithelial duct surrounded by blood vessels and composed of a basement membrane and one internal layer of epithelial cells. Our results show that an increment in the order of 8-fold in glucose metabolism and an increase in acid resistance corresponding to pH thresholds of approximately 6.8 and 6.45 for quiescence and death, respectively, are required for the tumor to breach through the layer of healthy epithelia] cells and reach the basement membrane as a first step for invasion.