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Exact Identity Linking Entropy Production and Mutual Information

Doohyeong Cho, Hawoong Jeong

Abstract

Linking entropy production (EP) to information is a key step toward data-driven nonequilibrium thermodynamics. We derive an exact identity for overdamped Langevin dynamics that equates the total EP rate to the mutual-information rate between an infinitesimal displacement and its time-symmetric midpoint, up to a bulk mean-flow contribution. This mapping elevates information theory to a thermodynamic calculus: the chain rule yields a canonical, nonnegative split into self and interaction EP, and leads to a tighter bound on learning rate with interaction EP as the necessary cost. As a proof of concept, applying the estimator to red-blood-cell flickering shows that interaction EP robustly exposes active signatures that conventional summaries can miss.

Exact Identity Linking Entropy Production and Mutual Information

Abstract

Linking entropy production (EP) to information is a key step toward data-driven nonequilibrium thermodynamics. We derive an exact identity for overdamped Langevin dynamics that equates the total EP rate to the mutual-information rate between an infinitesimal displacement and its time-symmetric midpoint, up to a bulk mean-flow contribution. This mapping elevates information theory to a thermodynamic calculus: the chain rule yields a canonical, nonnegative split into self and interaction EP, and leads to a tighter bound on learning rate with interaction EP as the necessary cost. As a proof of concept, applying the estimator to red-blood-cell flickering shows that interaction EP robustly exposes active signatures that conventional summaries can miss.
Paper Structure (10 equations, 4 figures)

This paper contains 10 equations, 4 figures.

Figures (4)

  • Figure 1: Schematic illustration of displacement $\Delta\bm{x}$ conditioned on $\bm{x}_m$. (Left) In equilibrium, detailed balance (DB) implies that $\bm{x}_m$ contains no information about $\Delta\bm{x}$. (Right) In nonequilibrium, a finite local mean velocity $\bm{v}_t(\bm{x}_m)$ breaks DB and biases $\Delta\bm{x}$ conditioned on $\bm{x}_m$, rendering the midpoint informative. In the infinitesimal-time limit $\mathrm{d}t\to 0$, $\Delta\bm{x}$ corresponds to $\mathrm{d}\bm{x}$ in the main text.
  • Figure 2: Physical mechanism and numerical validation of Eq. \ref{['eq:main_identity']}. (a–-e) Linear model defined by $\dot{x}=-kx+(s+a)y+\xi_{x}$ and $\dot{y}=-ky+(s-a)x+\xi_{y}$ with $k=10$ and $\boldsymbol{\mathsf{D}}=\mathbf{I}$. Parameters are $(s,a)=(5,0)$ for equilibrium (a, c), $(0,50)$ for nonequilibrium steady state (NESS) (b, d), and $s=0$ for (e). (a, b) Drift $\bm{F}(\bm{x})$ (black) and local mean velocity $\bm{v}(\bm{x})$ (yellow) overlaid on steady-state density $p(\bm{x})$. Crosses indicate sampling locations for time midpoint $\bm{x}_{m}$. (c, d) Conditional displacements $\Delta\bm{x}|\bm{x}_{m}$ at the marked locations. Circles are centered at sample means with radius $1.96\times\mathrm{SD}$; dashed lines mark the means and black solid lines denote the origin. In equilibrium (c), distributions are indistinguishable. In NESS (d), they separate by the local mean velocity $\bm{v}(\bm{x}_{m})\Delta t$, rendering $\bm{x}_{m}$ informative about $\Delta\bm{x}$. ($\Delta t=10^{-3}$ in simulations) (e, f) Convergence of information rates $4\,I(\Delta\bm{x};\bm{x}_m)/\Delta t$ (dotted) to the total EP rate (solid) as $\Delta t \to 0$. (f) Nonlinear model $\dot{x}=-x+y+\epsilon y^{3}+\xi_{x}$, $\dot{y}=-y+\xi_{y}$. Eq. \ref{['eq:main_identity']} remains exact in both linear and nonlinear models.
  • Figure 3: Information-theoretic EP decomposition and learning-rate bound in linear models. (a) Cascade model $\dot{x}=-k_x x + \alpha y + \xi_x$, $\dot{y}=-k_y y + \beta z + \xi_y$, and $\dot{z}=-k_z z + \xi_z$, partitioned into $A=\{x,y\}$ (blue) and $B=\{z\}$ (green). The coupling $\alpha$ controls internal within $A$ (not necessarily symmetric), while $\beta$ drives $A$ from $B$. (b, c) Local EP rate $\sigma_\mathrm{A}$ (solid blue) and its nonnegative components, self $\sigma_A^{\mathrm{self}}$ (dashed blue) and interaction $\sigma_{A|B}^{\mathrm{int}}$ (dashed orange), as functions of coupling strength ($k_{x,y,z}=2$); the black solid line denotes the total EP $\sigma_{\mathrm{AB}}$. (b) Varying $\alpha$ (with $\beta=1$) predominantly increases $\sigma_A^{\mathrm{self}}$, while $\sigma_{A|B}^{\mathrm{int}}$ remains nearly unchanged. (c) Varying $\beta$ (with $\alpha=1$) selectively increases $\sigma_{A|B}^{\mathrm{int}}$ with minimal change in $\sigma_A^{\mathrm{self}}$. (d) Numerical illustration of the system-level learning-rate bound Eq.\ref{['eq:tight_bound_total']} for linear Langevin dynamics $\dot{\bm{x}}=\boldsymbol{\mathsf{A}}\bm{x}+\sqrt{2\boldsymbol{\mathsf{D}}}\,\bm{\xi}$. We randomly sample stable $\boldsymbol{\mathsf{A}}$ and diagonal $\boldsymbol{\mathsf{D}}$, together with random bipartitions $A\cup B=\{1,\dots,d\}$ (see SM), and plot the ratio$|\dot I^{\mathrm A}|^{2}\mathcal{R}_{\mathrm{AB}}/\sigma^{\mathrm{int}}_{AB}$ versus $\sigma^{\mathrm{int}}_{AB}$ (log scale). Colors indicate dimension $d$; the dashed line marks saturation at unity.
  • Figure 4: Application to OT-sensing RBC fluctuations terlizzi2024variance. (a) Schematic (not to scale) of the OT-sensing setup and the effective coordinates: measured outer-membrane $x$, hidden membrane--cortex attachment $y$, and a stochastic active force $\eta$ driving the cascade $\eta\!\to\! y\!\leftrightarrow\! x$. (b) Tightness ratios $\rho_{\mathrm{tot}}$ and $\rho_{\mathrm{int}}$ [Eq. \ref{['eq:Q_definitions']}] for passive (blue) and active (red) cells, evaluated using the parameter values reported in Ref. terlizzi2024variance. Each colored marker denotes one cell. Active cells cluster markedly closer to saturation in $\rho_{\mathrm{int}}$, whereas passive cells remain far from it.