How should we reason with causal relationships? Much recent work on this question has been devoted to the theses (i) that Bayesian nets provide a calculus for causal reasoning and (ii) that we can learn causal relationships by the automated learning of Bayesian nets from observational data. The aim of this book is to..

This paper (based on joint work with M.J.Schervish and J.B.Kadane) discusses some differences between the received theory of regular conditional distributions, which is the countably additive theory of conditional probability, and a rival theory of conditional probability using the theory of finitely additive probability. The focus of the paper is maximally "improper" conditional probability distributions, where the received theory requires, in effect, that P{a: P(a|a) = 0} = 1. This work builds upon the results of Blackwell and Dubins (1975).

Evolutionary theory is awash with probabilities. For example, natural selection is said to occur when there is variation in fitness, and fitness is standardly decomposed into two components, viability and fertility, each of which is understood probabilistically. With respect to viability, a fertilized egg is said to have a certain chance of surviving to reproductive age; with respect to fertility, an adult is said to have an expected number of offspring.1 There is more to evolutionary theory than the theory of (...) natural selection, and here too one finds probabilistic concepts aplenty. When there is no selection, the theory of neutral evolution says that a gene’s chance of eventually reaching fixation is 1/(2N), where N is the number of organisms in the generation of the diploid population to which the gene belongs. The evolutionary consequences of mutation are likewise conceptualized in terms of the probability per unit time a gene has of changing from one state to another. The examples just mentioned are all “forwarddirected” probabilities; they describe the probability of later events, conditional on earlier events. However, evolutionary theory also uses “backwards probabilities” that describe the probability of a cause conditional on its effects; for example, coalescence theory allows one to calculate the expected number of generations in the past that the genes in the present generation find their most recent common ancestor. (shrink)

This paper discusses some differences between the received theory of regular conditional distributions, which is the countably additive theory of conditional probability, and a rival theory of conditional probability using the theory of finitely additive probability. The focus of the paper is maximally "improper" conditional probability distributions, where the received theory requires, in effect, that P{a: P = 0} = 1. This work builds upon the results of Blackwell and Dubins.