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Register a new userA shell model of eye growth and elasticity
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The eye grows during childhood to position the retina at the correct distance behind the lens to enable focused vision, a process called emmetropization. Animal studies have demonstrated that this growth process is dependent upon visual stimuli, while genetic and environmental factors that affect the likelihood of developing myopia have also been identified. The coupling between growth, remodeling and elastic response in the eye is particularly challenging to understand. To analyse this coupling, we develop a simple model of an eye growing under intraocular pressure in response to visual stimuli. Distinct to existing three-dimensional finite-element models of the eye, we treat the sclera as a thin axisymmetric hyperelastic shell which undergoes local growth in response to external stimulus. This simplified analytic model provides a tractable framework in which to evaluate various emmetropization hypotheses and understand different types of growth feedback, which we exemplify by demonstrating that local growth laws are sufficient to tune the global size and shape of the eye for focused vision across a range of parameter values.
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A new model of crystal growth is presented that describes the phenomena on atomic length and diffusive time scales. The former incorporates elastic and plastic deformation in a natural manner, and the latter enables access to times scales much larger than conventional atomic methods. The model is shown to be consistent with the predictions of Read and Shockley for grain boundary energy, and Matthews and Blakeslee for misfit dislocations in epitaxial growth.
Single-molecule experiments in which force is applied to DNA or RNA molecules have enabled important discoveries of nucleic acid properties and nucleic acid-enzyme interactions. These experiments rely on a model of the polymer force-extension behavior to calibrate the experiments; typically the experiments use the worm-like chain (WLC) theory for double-stranded DNA and RNA. This theory agrees well with experiments for long molecules. Recent single-molecule experiments have used shorter molecules, with contour lengths in the range of 1-10 persistence lengths. Most WLC theory calculations to date have assumed infinite molecule lengths, and do not agree well with experiments on shorter chains. Key physical effects that become important when shorter molecules are used include (i) boundary conditions which constrain the allowed fluctuations at the ends of the molecule and (ii) rotational fluctuations of the bead to which the polymer is attached, which change the apparent extension of the molecule. We describe the finite worm-like chain (FWLC) theory, which takes into account these effects. We show the FWLC predictions diverge from the classic WLC solution for molecules with contour lengths a few times the persistence length. Thus the FWLC will allow more accurate experimental calibration for relatively short molecules, facilitating future discoveries in single-molecule force microscopy.
A polymer network can imbibe water, forming an aggregate called hydrogel, and undergo large and inhomogeneous deformation with external mechanical constraint. Due to the large deformation, nonlinearity plays a crucial role, which also causes the mathematical difficulty for obtaining analytical solutions. Based on an existing model for equilibrium states of a swollen hydrogel with a core-shell structure, this paper seeks analytical solutions of the deformations by perturbation methods for three cases, i.e. free-swelling, nearly free-swelling and general inhomogeneous swelling. Particularly for the general inhomogeneous swelling, we introduce an extended method of matched asymptotics to construct the analytical solution of the governing nonlinear second-order variable-coefficient differential equation. The analytical solution captures the boundary layer behavior of the deformation. Also, analytical formulas for the radial and hoop stretches and stresses are obtained at the two boundary surfaces of the shell, making the influence of the parameters explicit. An interesting finding is that the deformation is characterized by a single material parameter (called the hydrogel deformation constant), although the free-energy function for the hydrogel contains two material parameters. Comparisons with numerical solutions are also made and good agreements are found.
We investigate the morphology of thin discs and rings growing in the circumferential direction. Recent analytical results suggest that this growth produces symmetric excess cones (e-cones). We study the stability of such solutions considering self-contact and bending stress. We show that, contrary to what was assumed in previous analytical solutions, beyond a critical growth factor, no symmetric textit{e}-cone solution is energetically minimal any more. Instead, we obtain skewed e-cone solutions having lower energy, characterized by a skewness angle and repetitive spiral winding with increasing growth. These results are generalized to discs with varying thickness and rings with holes of different radii.
When DNA molecules are heated they denature. This occurs locally so that loops of molten single DNA strands form, connected by intact double-stranded DNA pieces. The properties of this melting transition have been intensively investigated. Recently there has been a surge of interest in this question, caused by experiments determining the properties of partially bound DNA confined to nanochannels. But how does such confinement affect the melting transition? To answer this question we introduce, and solve a model predicting how confinement affects the melting transition for a simple model system by first disregarding the effect of self-avoidance. We find that the transition is smoother for narrower channels. By means of Monte-Carlo simulations we then show that a model incorporating self-avoidance shows qualitatively the same behaviour and that the effect of confinement is stronger than in the ideal case.
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