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In this chapter, we introduce various modeling approaches capable of addressing pattern formation by cell populations. Firstly, we discuss the Delta–Notch system as an example of pattern formation by local interaction. We then explore the Kessler–Levin model, which combines cellular automaton and continuous system approaches, illustrating the evolution of cAMP waves in cellular slime molds. Next, our attention turns to methodologies requiring active consideration of cellular arrangements and deformations, including models involving cell proliferation and movement. We present reaction–diffusion systems that explain structures formed in bacterial colonies resembling Diffusion Limited Aggregation (DLA). Additionally, we introduce the cellular Potts model to investigate pattern formation among moving cells, incorporating variations in cellular adhesion force. The cell-vertex model represents a cell population as a collection of vertices of a polygon or polyhedron. We also discuss the phase field model, employing partial differential equations to depict relatively simple morphological changes in complex structures. By employing these modeling techniques, we can capture the characteristics of various pattern formations orchestrated by cell populations.
The chapter illustrates what it meant for Carolyn Beatrice Parker (1917–1966) to be a Black woman physicist in the US during the Jim Crow era. Her father, a physician, and her mother, a teacher, shepherded her into Fisk University, an historically Black college. As a physics major she studied infrared spectroscopy with the Black physicist Elmer Imes, graduating with a BS in 1938. She later attended the University of Michigan, obtaining an MA in physics in 1941. But like many Black women, she spent time before and after graduate school teaching in the K–12 system. In 1943, she became a research physicist at the Aircraft Radio Laboratory in Dayton, Ohio, where she stayed for four years. Although she co-authored a governmental report about her work on signal attenuation in coaxial cables, her name only appeared in the acknowledgments of the ensuing academic publications, thus partly obscuring her contributions. In 1947, Fisk University welcomed Parker on the faculty, but she soon after enrolled in a nuclear physics PhD program at the Massachusetts Institute of Technology. After dropping out, she worked as a laboratory technician until she grew too ill and died a short time later.
When a quantum system has some external time dependence, some rather special things happen. This chapter explores this subject. Among the topics that we cover are the adiabatic theorem, Berry phase, the sudden approximation, and time-dependent perturbation theory.
There are two great equations of classical physics: one is Einstein’s equation of general relativity, the other the Navier-Stokes equation that describes how fluids flow. In this chapter, we meet Navier-Stokes.
This equation differs from the Euler equation by the addition of a viscosity term. This is not a small change and makes solutions to the Navier-Stokes equation much richer and more subtle than those of the Euler equation. In this chapter, we begin our exploration of these solutions.
Active particles self-propel through some intrinsic mechanism. First, a simple one-dimensional model is introduced for which the density profile between confining walls and the pressure exerted on these walls can be calculated analytically. In three dimensions, run-and-tumble particles, active Brownian particles, and active Ornstein–Uhlenbeck particles constitute three classes of models that can be described by Langevin equations. The identification of entropy production in the steady state is shown to be ambiguous. The continuum limit of a thermodynamically consistent discrete model shows that Langevin descriptions contain some implicit coarse-graining which prevents the recovery of the full physical entropy production.
This chapter deals with correlation and response functions in equilibrium and in nonequilibrium steady states for a Langevin dynamics. First, the harmonic oscillator in equilibrium is discussed as a paradigmatic case. In the general nonlinear case, it is shown how time-derivatives in correlation functions can be replaced by state variables. The response function is derived within the path integral formalism. It can be expressed by various forms of a correlation function. One particularly transparent version restores the form of the equilibrium fluctuation-dissipation theorem for a nonequilibrium steady state. A second strategy to derive a response function starts with the perturbed Fokker–Plank operator. Causality imposes the Kramers–Kronig relations between the real and imaginary parts of the response function. Through the Harada–Sasa relation, the deviation from the equilibrium form of the fluctuation-dissipation relation can be related to the mean entropy production.
In this chapter, we explore theoretical aspects of the origin of life problem. Firstly, we address the Chicken and Egg problem referring to the “RNA world.” We explain a mathematical model of the RNA replication system introduced by Eigen and discuss the conditions necessary for self-replication, referring “error catastrophe.” As a potential solution, we discuss the “hypercycle,” alongside its vulnerabilities and the acquisition of evolvability through compartmentalization. On another front, we examine Dyson’s catalytic reaction system as an alternative hypothesis, showing that catalytic reaction networks capable of maintaining themselves and undergoing imperfect reproduction may have appeared first. We also refer to a simple model of polymer reactions, arguing that such autocatalytic reaction networks can stochastically emerge, as proposed by Kauffman. Furthermore, we describe a cell model featuring an intracellular chemical reaction network that divides based on its state, highlighting the universal nature of reaction dynamics in replicating cells and the power-law distribution of chemical abundance (Zipf’s law), which has been verified across many organisms. Additionally, we introduce the concept of “minority control” in catalytic reaction networks, which can carry primitive genetic information. Finally, we discuss perspectives on research regarding the origin of life.
This chapter serves as an intuitive introduction to dynamical systems within the realm of biological systems, through visual representations of state space dynamics. Biological examples and experimental realizations are described to demonstrate how dynamical systems concepts are applicable in solving fundamental problems in cell biology. Differential equations are taken as typical of dynamical systems, and we explain topics such as nullcline and fixed points, linear stability analysis, and attractors, elucidating their significance using systems such as gene toggle switches. The introduction of limit cycles and the Poincaré–Bendixson theorem in two-dimensional systems is followed by examples such as the Brusselator and the repressilator system. Furthermore, we explore the basin structure in multi-attractor systems and provide detailed explanations using toggle switch systems to illustrate time-scale separation between variables and adiabatic elimination of variables. Several instances of co-dimension 1 bifurcations commonly observed in biological systems are presented, with a discussion of their biological significance in processes like cell differentiation. Finally, chaos theory is introduced.
Viscous fingering instabilities, common in confined environments such as porous media or Hele-Shaw cells, surprisingly also occur in unconfined, non-porous settings as revealed by recent experiments. These novel instabilities involve free-surface flows of dissimilar viscosity. We demonstrate that such a free-surface flow, involving a thin film of viscous fluid spreading over a substrate that is prewetted with a fluid of higher viscosity, is susceptible to a similar type of novel viscous fingering instability. Such flows are relevant to a range of geophysical, industrial and physiological applications from the small scales of thin-film coating applications and nasal drug delivery to the large scales of lava flows. In developing a theoretical framework, we assume that the intruding layer and the liquid film over which it flows are both long and thin, the effects of inertia and surface tension are negligible, and both layers are driven by gravity and resisted by viscous shear stress so that the principles of lubrication theory hold. We investigate the stability of axisymmetric similarity solutions, describing the base flow, by examining the growth of small-amplitude non-axisymmetric perturbations. We characterise regions of instability across parameter space and find that these instabilities emerge above a critical viscosity ratio. That is, a fluid of low viscosity intruding into another fluid of sufficiently high viscosity is susceptible to instability, akin to traditional viscous fingering in a porous medium. We identify the mechanism of instability, compare with other frontal instabilities and demonstrate that high enough density differences suppress the instability completely.
For the Brownian motion of a particle in a fluid, the Langevin equation for its momentum is introduced phenomenologically. The strength of the noise is shown to be related to friction, and, in a second step, to the diffusion coefficient. Excellent agreement with experiments on a levitated particle in gas is demonstrated. This phenomenological Langevin equation is then shown to follow from a general projection approach to the underlying Hamiltonian dynamics of the full system in the limit of an infinite mass ratio between Brownian particles and fluid molecules. For Brownian motion in liquids, additional time-scales enter that are discussed phenomenologically and illustrated with experiments.