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Mathematical modelling has great potential to motivate students towards studying mathematics. This article discusses several different approaches to integrating research work with a second-year undergraduate, mathematical modelling subject. I found sourcing papers from the areas of epidemiology and ecology to be a fruitful source area, particularly models involving only two or three coupled differential equations. These models were amenable to students as well as interesting and relevant to students because they came from real research papers. I will describe the use of scenarios and case studies in lectures, and group projects for assessment. The scenarios and case studies were published in a textbook that I wrote. Scenarios, case studies and projects provided an opportunity to expose students to some novel applications of differential equations. One example is developed here as a Classroom Note: modelling the dynastic cycles in Chinese history. [ABSTRACT FROM AUTHOR]

An SEI metapopulation model is developed for the spread of an infectious agent by migration. The model portrays two age classes on a number of patches connected by migration routes which are used as host animals mature. A feature of this model is that the basic reproduction ratio may be computed directly, using a scheme that separates topography, demography, and epidemiology. We also provide formulas for individual patch basic reproduction numbers and discuss their connection with the basic reproduction ratio for the system. The model is applied to the problem of spatial spread of bovine tuberculosis in a possum population. The temporal dynamics of infection are investigated for some generic networks of migration links, and the basic reproduction ratio is computed—its value is not greatly different from that for a homogeneous model. Three scenarios are considered for the control of bovine tuberculosis in possums where the spatial aspect is shown to be crucial for the design of disease management operations. [Copyright &y& Elsevier]

Line distributions of Stokes flow singularities are used to model the flow around a slender body which is straddling a flat interface between two viscous fluids. Motion of the slender body parallel to the interface and normal to the interface is considered where the axis of symmetry of the slender body is always perpendicular to the undisturbed interface. Asymptotic approximations to the force distributions on the slender body are evaluated and the relative contributions of that part of the slender body in one fluid to the force distribution in the other fluid and of the interface interaction to the force distribution are examined. It is observed that a shielding region exists about the interface which is due to the interaction with that part of the slender body in the other fluid. Finally, for parallel motion, the first order interface deformation is calculated. [ABSTRACT FROM PUBLISHER]

A possible method of control for the management of wild populations consists of continual introgression of an inducible transgene by releasing transgenic individuals, with periodic exposure of the population to a trigger. Exposure to the trigger causes death or sterility in carriers of the transgene, but is otherwise benign. We investigate the effectiveness of various strategies for control. We show that suppression of the population density below any pre-specified level is possible using this technique. At the same time we show that too frequent or too efficient exposure to the trigger can select for non-transgenic genotypes at an intensity such that the population density will be largely unaffected by the trigger. Choices for management parameters can ensure that the latter scenario is avoided. We show that releasing individuals carrying the transgene at more than one locus facilitates density control., (Copyright 2000 Academic Press.)

A modified resistive force theory is developed for a spermatozoon swimming in a general linear viscoelastic fluid. The theory is based on a Fourier decomposition of the flagellar velocity, which leads to solving the Stokes flow equations with a complex viscosity. We use a model spermatozoon with a spherical head which propagates small amplitude sinusoidal waves along its flagellum. Results are obtained for the velocity of propulsion and the rate of working for a free swimming spermatozoon and the thrust on a fixed spermatozoon. There is no change in propulsive velocity for a viscoelastic fluid compared to a Newtonian fluid. The rate of working does change however, decreasing with increasing elasticity of the fluid, for a Maxwell fluid. Thus the theory predicts that a spermatozoon can swim faster in a Maxwell fluid with the same expenditure of energy for a Newtonian fluid.

A fluid mechanical model is developed for the filtering mechanism in mussels that enables estimates to be made of the pressure drop through the gill filaments due to (i) the latero-frontal filtering cilia, (ii) the lateral (pumping) cilia and through the non-ciliated zone at the ventral end of the filament. Calculations indicate that the lateral cilia can generate a sufficient pressure change to 'pump' water through the gill filaments. The velocity profile across the filaments indicates that a backflow can occur in the centre of the channel. Normally the latero-frontal cilia would damp out this backflow but in the case when all the cilia are upright, two 'standing' eddies may form at the mouth of the channel, forcing the incoming water to the side.

A two-layer Newtonian fluid model for muco-ciliary transport in the lung is developed where the viscosity of the upper mucous layer is very much greater than the viscosity of the lower periciliary layer. Theory is presented for both cases when the cilia penetrate, and do not penetrate, the very viscous mucous layer. Calculations suggest that, in normal circumstances, it is not essential for the cilia to penetrate the mucus to provide positive transport. However, it does suggest that there is a weak optimal penetration depth of the cilia of between 10-20% of the cilium length. In the case of high ciliary inactivity (e.g. 90% inactive), penetration of cilia into the mucus is essential for normal transport rates suggesting the mucociliary system may be deliberately overdesigned to cater for a whole range of pathological circumstances.