This paper presents a review and classification of traffic assignment models for strategic transport planning purposes by using concepts analogous to genetics in biology. Traffic assignment models share the same theoretical framework (DNA), but differ in functionality (genes). We argue that all traffic assignment models can be described by two genes. The first gene determines the spatial functionality (unrestricted, capacity restrained, capacity constrained, capacity and storage constrained) described by five spatial interaction assumptions, while the second gene determines the temporal functionality (static, semi-dynamic, dynamic) described by two temporal interaction assumptions. This classification provides a deeper understanding of the often implicit assumptions made in traffic assignment models described in the literature, particularly with respect to networking loading where the largest differences occur. It further allows for comparing different models in terms of functionality, and opens the way for developing novel traffic assignment models.
This paper presents a novel idealised dynamical model of day to day traffic re-routeing (as traffic seeks cheaper routes) and proves a stability result for this dynamical model. (The dynamical model is based on swapping flow between paired alternative segments (these were introduced by Bar Gera (2010)) rather than between routes.) It is shown that under certain conditions the dynamical system enters a given connected set of approximate equilibria in a finite number of days or steps. This proof allows for saturation flows which act as potentially active flow constraints. The dynamical system involving paired alternative segment swaps is then combined with a novel green-time-swapping rule; this rule swaps green-time toward more pressurised signal stages. It is shown that if (i) the delay formulae have a simple form and (ii) the "pressure" formula fits the special control policy P 0 (see Smith, 1979a, b), then the combined flow-swapping / green-time-swapping dynamical model also enters a given connected set of approximate consistent equilibria in a finite number of steps. Computational results confirm, in a simple network, the positive P 0 result and also show, on the other hand, that such good behaviour may not arise if the equi-saturation control policy is utilized. The dynamical models described here do not represent blocking back effects.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.