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Biology subjects

Binny, R. N.

Publications and source records attributed to Binny, R. N..

2 recordsLinked to original sources

Small-scale spatial structure influences large-scale invasion rates

Local interactions among individual members of a population can generate intricate small-scale spatial structure, which can strongly influence population dynamics. The two-way interplay between local interactions and population dynamics is well understood in the relatively simple case where the population occupies a fixed domain with a uniform average density. However, the situation where the average population density is spatially varying is less well understood. This situation includes ecologically important scenarios such as species invasions, range shifts, and moving population fronts. Here, we investigate the dynamics of the spatial stochastic logistic model in a scenario where an initially confined population subsequently invades new, previously unoccupied territory. This simple model combines density-independent proliferation with dispersal, and density-dependent mortality via competition with other members of the population. We show that, depending on the spatial scales of dispersal and competition, either a clustered or a regular spatial structure develops over time within the invading population. In the short-range dispersal case, the invasion speed is significantly lower than standard predictions of the mean-field model. We conclude that mean-field models, even when they account for non-local processes such as dispersal and competition, can give misleading predictions for the speed of a moving invasion front.

cell biology↗

Inferring parameters for a lattice-free model of cell migration and proliferation using experimental data

Collective cell spreading takes place in spatially continuous environments, yet it is often modelled using discrete lattice-based approaches. Here, we use data from a series of cell proliferation assays, with a prostate cancer cell line, to calibrate a spatially continuous individual based model (IBM) of collective cell migration and proliferation. The IBM explicitly accounts for crowding effects by modifying the rate of movement, direction of movement, and the rate of proliferation by accounting for pair-wise interactions. Taking a Bayesian approach we estimate the free parameters in the IBM using rejection sampling on three separate, independent experimental data sets. Since the posterior distributions for each experiment are similar, we perform simulations with parameters sampled from a new posterior distribution generated by combining the three data sets. To explore the predictive power of the calibrated IBM, we forecast the evolution of a fourth experimental data set. Overall, we show how to calibrate a lattice-free IBM to experimental data, and our work highlights the importance of interactions between individuals. Despite great care taken to distribute cells as uniformly as possible experimentally, we find evidence of significant spatial clustering over short distances, suggesting that standard mean-field models could be inappropriate.

cell biology↗