Thomas H. Solomon
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Thomas H. Solomon has a total of 25 co-authors. Here are the top co-authors by number of shared publications:
- Kevin A. Mitchell
University of California, Merced
5 shared publications M. S. Paoletti
Department of Physics, Bucknell University, Lewisburg, Pennsylvania 17837, USA
3 shared publications- Mollie E. Schwartz
Lincoln Laboratory, Massachusetts Institute of Technology, Lexington, USA
3 shared publications C. R. Nugent
Department of Physics, Bucknell University, Lewisburg, Pennsylvania 17837, USA
2 shared publications- Taylor J. Whitney
University of California, Merced
2 shared publications - A. T. Lee
Department of Physics, Bucknell University, Lewisburg, Pennsylvania 17837
1 shared publication
Latest Publications
- 22 September 2025
- Published by American Physical Society (APS) in Physical Review E
- Vol. 112 (3) , 034412
General approach to the statistics of microbial orientation: Lévy walks, noise, and deterministic drift
Microbial motion is typically analyzed by simplified models in which trajectories exhibit straight runs (perhaps with added Gaussian noise) followed by random, discrete tumbling events. We present the results of a statistical analysis of the angular dynamics for four different swimming microbes: tumbling and smooth-swimming strains of Bacillus subtilis and two Eukaryotic algae, Tetraselmis suecica and Euglena gracilis. We show that the angular statistics closely resemble a Voigt profile, the convolution of a Gaussian (Lévy index α=2) and Lorentzian (Lévy index α=1) distribution. This distribution is ubiquitous for all four microbes. Rather than modeling tumbling as a discrete process, we model tumbling dynamics as a continuous process: Lévy flights in the orientational dynamics using a Lorentzian noise model. This model is analytically solvable. Each individual microbe trajectory has both stochastic behavior (noise) and varying drift behavior, such as helices of different sizes and frequencies and circular arcs with different radii. We model the distribution of different drift behavior via an ensemble theory. The drift behavior (e.g., circular arcs) comes from physical observations of the swimming behavior and explains many of the qualitative features of the experimental data that cannot be explained by a pure noise model. From this theory, we estimate the strength of Lorentzian noise, the physical rotational diffusion constant, and some relevant parameters relating to the distributions of deterministic drift behavior. This analysis shows that in some cases Gaussian noise is not the dominant process responsible for the angular statistics following a Voigt profile.
- 22 September 2025
- Published by American Physical Society (APS) in Physical Review E
- Vol. 112 (3) , 034412
General approach to the statistics of microbial orientation: Lévy walks, noise, and deterministic drift
Microbial motion is typically analyzed by simplified models in which trajectories exhibit straight runs (perhaps with added Gaussian noise) followed by random, discrete tumbling events. We present the results of a statistical analysis of the angular dynamics for four different swimming microbes: tumbling and smooth-swimming strains of Bacillus subtilis and two Eukaryotic algae, Tetraselmis suecica and Euglena gracilis. We show that the angular statistics closely resemble a Voigt profile, the convolution of a Gaussian (Lévy index α=2) and Lorentzian (Lévy index α=1) distribution. This distribution is ubiquitous for all four microbes. Rather than modeling tumbling as a discrete process, we model tumbling dynamics as a continuous process: Lévy flights in the orientational dynamics using a Lorentzian noise model. This model is analytically solvable. Each individual microbe trajectory has both stochastic behavior (noise) and varying drift behavior, such as helices of different sizes and frequencies and circular arcs with different radii. We model the distribution of different drift behavior via an ensemble theory. The drift behavior (e.g., circular arcs) comes from physical observations of the swimming behavior and explains many of the qualitative features of the experimental data that cannot be explained by a pure noise model. From this theory, we estimate the strength of Lorentzian noise, the physical rotational diffusion constant, and some relevant parameters relating to the distributions of deterministic drift behavior. This analysis shows that in some cases Gaussian noise is not the dominant process responsible for the angular statistics following a Voigt profile.
- Open Access
- 1 June 2025
- Published by AIP Publishing in Chaos: An Interdisciplinary Journal of Nonlinear Science
- Vol. 35 (6)
Chaos, dynamic trapping, and transport of swimming microbes in a vortex chain flow
We present experiments on chaotic motion of self-propelled (active) particles in a time-independent, two-dimensional vortex chain flow. We track Tetraselmis microbes and calculate the variance of a spreading distribution of these microbes in the flow. For small non-dimensional swimming speed v0, we find subdiffusion with variance ⟨x2⟩∼tγ with γ<1; transport is diffusive (γ=1) for larger v0. Subdiffusion for small v0 is due to dynamic trapping of microbes to islands of ordered trajectories surrounded by a sea of chaotic motion; these islands disappear for larger v0. We calculate Lagrangian-averaged trajectories (LATs) from the experimental data and use the LATs to measure trapping time probability distributions P(t). We find regimes with P(t)∼t−ν with ν<2 for small v0, consistent with the measured subdiffusion.
- 1 June 2025
- Published by AIP Publishing in Chaos: An Interdisciplinary Journal of Nonlinear Science
- Vol. 35 (6)
Open AccessChaos, dynamic trapping, and transport of swimming microbes in a vortex chain flow
We present experiments on chaotic motion of self-propelled (active) particles in a time-independent, two-dimensional vortex chain flow. We track Tetraselmis microbes and calculate the variance of a spreading distribution of these microbes in the flow. For small non-dimensional swimming speed v0, we find subdiffusion with variance ⟨x2⟩∼tγ with γ<1; transport is diffusive (γ=1) for larger v0. Subdiffusion for small v0 is due to dynamic trapping of microbes to islands of ordered trajectories surrounded by a sea of chaotic motion; these islands disappear for larger v0. We calculate Lagrangian-averaged trajectories (LATs) from the experimental data and use the LATs to measure trapping time probability distributions P(t). We find regimes with P(t)∼t−ν with ν<2 for small v0, consistent with the measured subdiffusion.
- Open Access
A general approach to the statistics of microbial orientation: Lévy walks, noise, and deterministic motion
Microbial motion is typically analyzed by simplified models in which trajectories exhibit straight runs (perhaps with added Gaussian noise) followed by random, discrete tumbling events. We present the results of a statistical analysis of the angular dynamics for four different swimming microbes: tumbling and smooth-swimming strains of \textit{Bacillus subtilis} and two Eukaryotic algae, \textit{Tetraselmis suecica} and \textit{Euglena gracilis}. We show that the angular statistics closely resemble a Voigt profile, the convolution of a Gaussian (Lévy index $α=2$) and Lorentzian (Lévy index $α=1$) distribution. This distribution is ubiquitous for all four microbes. Rather than modeling tumbling as a discrete process, we model tumbling dynamics as a continuous process: Lévy flights in the orientational dynamics using a Lorentzian noise model. This model is analytically solvable. Each individual microbe trajectory has both stochastic behavior (noise) and varying deterministic behavior, such as helices of different sizes and frequencies and circular arcs with different radii. We model the distribution of different deterministic behavior via an ensemble theory. The deterministic behavior (e.g., circular arcs) comes from physical observations of the swimming behavior and explains many of the qualitative features in the data that cannot be explained by a pure noise model. From this theory, we estimate the strength of Lorentzian noise, the physical rotational diffusion constant, and some relevant parameters relating to the distributions of deterministic behavior. This analysis shows that in some cases Gaussian noise is not the dominant process responsible for the angular statistics following a Voigt profile.
Open AccessA general approach to the statistics of microbial orientation: Lévy walks, noise, and deterministic motion
Microbial motion is typically analyzed by simplified models in which trajectories exhibit straight runs (perhaps with added Gaussian noise) followed by random, discrete tumbling events. We present the results of a statistical analysis of the angular dynamics for four different swimming microbes: tumbling and smooth-swimming strains of \textit{Bacillus subtilis} and two Eukaryotic algae, \textit{Tetraselmis suecica} and \textit{Euglena gracilis}. We show that the angular statistics closely resemble a Voigt profile, the convolution of a Gaussian (Lévy index $α=2$) and Lorentzian (Lévy index $α=1$) distribution. This distribution is ubiquitous for all four microbes. Rather than modeling tumbling as a discrete process, we model tumbling dynamics as a continuous process: Lévy flights in the orientational dynamics using a Lorentzian noise model. This model is analytically solvable. Each individual microbe trajectory has both stochastic behavior (noise) and varying deterministic behavior, such as helices of different sizes and frequencies and circular arcs with different radii. We model the distribution of different deterministic behavior via an ensemble theory. The deterministic behavior (e.g., circular arcs) comes from physical observations of the swimming behavior and explains many of the qualitative features in the data that cannot be explained by a pure noise model. From this theory, we estimate the strength of Lorentzian noise, the physical rotational diffusion constant, and some relevant parameters relating to the distributions of deterministic behavior. This analysis shows that in some cases Gaussian noise is not the dominant process responsible for the angular statistics following a Voigt profile.
- 3 May 2024
- Published by American Physical Society (APS) in Physical Review Fluids
- Vol. 9 (5) , 054501
Barriers and chutes for mixing of active particles in a vortex chain flow
We present experiments on the mixing of active particles—swimming Tetraselmis microbes—in a microfluidic vortex chain flow, driven magnetohydrodynamically. We track the microbes in the flow and interpret the resulting trajectories in terms of a theory of swimming invariant manifolds (SwIMs), a generalization of invariant manifold theories developed originally to characterize mixing of passive tracers. The experiments verify predictions that SwIMs act as barriers in a three-dimensional phase space. Projected onto position space, edges of the manifolds (SwIM-edges) are one-way barriers that impede the motion of the microbes in one direction but allow them to pass freely in the other. Pairs of SwIMs combine to form chutes that carry microbes between vortices. For short times, the experimentally measured intervortex flux agrees well with theoretical predictions based on the cross-sectional area of the chutes, despite experimental evidence of nonuniformities in the microbe density, due to deviations of the microbes from a perfect circular shape.- 3 May 2024
- Published by American Physical Society (APS) in Physical Review Fluids
- Vol. 9 (5) , 054501
Barriers and chutes for mixing of active particles in a vortex chain flow
We present experiments on the mixing of active particles—swimming Tetraselmis microbes—in a microfluidic vortex chain flow, driven magnetohydrodynamically. We track the microbes in the flow and interpret the resulting trajectories in terms of a theory of swimming invariant manifolds (SwIMs), a generalization of invariant manifold theories developed originally to characterize mixing of passive tracers. The experiments verify predictions that SwIMs act as barriers in a three-dimensional phase space. Projected onto position space, edges of the manifolds (SwIM-edges) are one-way barriers that impede the motion of the microbes in one direction but allow them to pass freely in the other. Pairs of SwIMs combine to form chutes that carry microbes between vortices. For short times, the experimentally measured intervortex flux agrees well with theoretical predictions based on the cross-sectional area of the chutes, despite experimental evidence of nonuniformities in the microbe density, due to deviations of the microbes from a perfect circular shape.- 17 May 2022
- Published by Springer Nature
- p. 99-119
Nonlinear Fluid Flow, Pattern Formation, Mixing, and Turbulence
- 17 May 2022
- Published by Springer Nature
- p. 99-119
Nonlinear Fluid Flow, Pattern Formation, Mixing, and Turbulence
- 14 January 2021
- Published by American Physical Society (APS) in Physical Review Fluids
- Vol. 6 (1) , L012501
Transport barriers to self-propelled particles in fluid flows
We present theory and experiments demonstrating the existence of invariant manifolds that impede the motion of microswimmers in two-dimensional fluid flows. One-way barriers are apparent in a hyperbolic fluid flow that block the swimming of both smooth-swimming and run-and-tumble Bacillus subtilis bacteria. We identify key phase-space structures, called swimming invariant manifolds (SwIMs), that serve as separatrices between different regions of long-time swimmer behavior. When projected into space, the edges of the SwIMs act as one-way barriers, consistent with the experiments.- 14 January 2021
- Published by American Physical Society (APS) in Physical Review Fluids
- Vol. 6 (1) , L012501
Transport barriers to self-propelled particles in fluid flows
We present theory and experiments demonstrating the existence of invariant manifolds that impede the motion of microswimmers in two-dimensional fluid flows. One-way barriers are apparent in a hyperbolic fluid flow that block the swimming of both smooth-swimming and run-and-tumble Bacillus subtilis bacteria. We identify key phase-space structures, called swimming invariant manifolds (SwIMs), that serve as separatrices between different regions of long-time swimmer behavior. When projected into space, the edges of the SwIMs act as one-way barriers, consistent with the experiments.- 10 June 2020
- Published by Springer Nature
- p. 1-21
Nonlinear Fluid Flow, Pattern Formation, Mixing, and Turbulence
- 10 June 2020
- Published by Springer Nature
- p. 1-21
Nonlinear Fluid Flow, Pattern Formation, Mixing, and Turbulence
- Open Access
- 26 March 2018
- Published by American Physical Society (APS) in Physical Review E
- Vol. 97 (3) , 033111
Barriers to front propagation in laminar, three-dimensional fluid flows
We present experiments on one-way barriers that block reaction fronts in a fully three-dimensional (3D) fluid flow. Fluorescent Belousov-Zhabotinsky reaction fronts are imaged with laser-scanning in a laminar, overlapping vortex flow. The barriers are analyzed with a 3D extension to burning invariant manifold (BIM) theory that was previously applied to two-dimensional advection-reaction-diffusion processes. We discover tube and sheet barriers that guide the front evolution. The experimentally determined barriers are explained by BIMs calculated from a model of the flow.
- 26 March 2018
- Published by American Physical Society (APS) in Physical Review E
- Vol. 97 (3) , 033111
Open AccessBarriers to front propagation in laminar, three-dimensional fluid flows
We present experiments on one-way barriers that block reaction fronts in a fully three-dimensional (3D) fluid flow. Fluorescent Belousov-Zhabotinsky reaction fronts are imaged with laser-scanning in a laminar, overlapping vortex flow. The barriers are analyzed with a 3D extension to burning invariant manifold (BIM) theory that was previously applied to two-dimensional advection-reaction-diffusion processes. We discover tube and sheet barriers that guide the front evolution. The experimentally determined barriers are explained by BIMs calculated from a model of the flow.
- 31 December 2011
- Published by Elsevier in Communications in Nonlinear Science and Numerical Simulation
- Vol. 16 (12) , 4558-4563
Pinning and mode-locking of reaction fronts by vortices
- 31 December 2011
- Published by Elsevier in Communications in Nonlinear Science and Numerical Simulation
- Vol. 16 (12) , 4558-4563
Pinning and mode-locking of reaction fronts by vortices
- 21 August 2008
- Published by IOP Publishing in Europhysics Letters
- Vol. 83 (5) , 58002
Fronts and trigger wave patterns in an array of oscillating vortices
We present experiments on reaction fronts and self-sustaining trigger wave patterns in an advection-reaction-diffusion system with chaotic mixing. The flow is a two-dimensional array of oscillating vortices, and the reaction is the excitable Belousov-Zhabotinsky chemical reaction. Reaction fronts are found to mode-lock for a wide range of frequencies, and the mode-locking results in "faceted" fronts that line up along the directions of the underlying vortex array. Self-sustaining trigger wave patterns are also found composed of large scale spiral and spiral-pair patterns, similar to patterns in the reaction-diffusion (no flow) limit but with a significantly larger typical length scale and with clear anisotropy that reflects the vortex array.
- 21 August 2008
- Published by IOP Publishing in Europhysics Letters
- Vol. 83 (5) , 58002
Fronts and trigger wave patterns in an array of oscillating vortices
We present experiments on reaction fronts and self-sustaining trigger wave patterns in an advection-reaction-diffusion system with chaotic mixing. The flow is a two-dimensional array of oscillating vortices, and the reaction is the excitable Belousov-Zhabotinsky chemical reaction. Reaction fronts are found to mode-lock for a wide range of frequencies, and the mode-locking results in "faceted" fronts that line up along the directions of the underlying vortex array. Self-sustaining trigger wave patterns are also found composed of large scale spiral and spiral-pair patterns, similar to patterns in the reaction-diffusion (no flow) limit but with a significantly larger typical length scale and with clear anisotropy that reflects the vortex array.