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Matrix population models are a specific type of population model that uses matrix algebra. Population models are used in population ecology to model the dynamics of wildlife or human populations. Matrix algebra, in turn, is simply a form of algebraic shorthand for summarizing a larger number of often repetitious and tedious algebraic computations.
Fitting of a noisy curve by an asymmetrical peak model, with an iterative process (Gauss–Newton algorithm with variable damping factor α). Curve fitting [ 1 ] [ 2 ] is the process of constructing a curve , or mathematical function , that has the best fit to a series of data points , [ 3 ] possibly subject to constraints.
Population biology is especially concerned with the Gompertz function. This function is especially useful in describing the rapid growth of a certain population of organisms while also being able to account for the eventual horizontal asymptote, once the carrying capacity is determined (plateau cell/population number). It is modeled as follows:
The iterative proportional fitting procedure (IPF or IPFP, also known as biproportional fitting or biproportion in statistics or economics (input-output analysis, etc.), RAS algorithm [1] in economics, raking in survey statistics, and matrix scaling in computer science) is the operation of finding the fitted matrix which is the closest to an initial matrix but with the row and column totals of ...
The Leslie matrix is a discrete, age-structured model of population growth that is very popular in population ecology named after Patrick H. Leslie. [1] [2] The Leslie matrix (also called the Leslie model) is one of the most well-known ways to describe the growth of populations (and their projected age distribution), in which a population is closed to migration, growing in an unlimited ...
P 0 = P(0) is the initial population size, r = the population growth rate, which Ronald Fisher called the Malthusian parameter of population growth in The Genetical Theory of Natural Selection, [2] and Alfred J. Lotka called the intrinsic rate of increase, [3] [4] t = time. The model can also be written in the form of a differential equation:
GEE estimates the average response over the population ("population-averaged" effects) with Liang-Zeger standard errors, and in individuals using Huber-White standard errors, also known as "robust standard error" or "sandwich variance" estimates. [3]
The r = 4 case of the logistic map is a nonlinear transformation of both the bit-shift map and the μ = 2 case of the tent map. If r > 4, this leads to negative population sizes. (This problem does not appear in the older Ricker model, which also exhibits chaotic dynamics.)