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Bistability

Bistability refers to the existence of two asymptotically stable fixed points in a deterministic dynamical model, where the system's final state is determined by its initial conditions, often separated by an unstable threshold and characterized by hysteresis in transitions between states.^[1] This phenomenon arises in diverse scientific domains due to nonlinear dynamics, such as positive feedback loops or mutual inhibition, enabling systems to maintain memory of prior states or exhibit switch-like behaviors. In biology, bistability is prevalent in gene regulatory networks, where it facilitates stochastic switching between high and low expression states (ON/OFF), promoting phenotypic heterogeneity that enhances adaptability in fluctuating environments.^[2] For instance, in bacteria like Bacillus subtilis and Escherichia coli, it underlies processes such as genetic competence for DNA uptake and persistence against antibiotics, allowing subpopulations to survive stresses without genetic changes.^[3] In cell signaling pathways, bistability supports all-or-none decision-making, such as in cell differentiation and cycle progression, and is implicated in diseases like cancer when disrupted.^[4] Beyond biology, bistability manifests in physical systems, including optical bistability in devices like Fabry-Pérot interferometers, where light intensity can settle into two stable transmission levels depending on input, enabling applications in optical switching.^[1] Magnetic bistability occurs in spin-crossover complexes, allowing reversible transitions between high- and low-spin states for data storage.^[1] In chemistry and ecology, it explains pattern formation in reaction-diffusion systems and alternative stable states in ecosystems, such as shifts between forested and degraded landscapes in tropical regions, with implications for resilience and tipping points.^[5] Overall, bistability's role in enabling robust, history-dependent responses underscores its importance across natural and engineered systems.

Introduction and Fundamentals

Definition and Basic Characteristics

Bistability refers to a property of certain dynamical systems in which there exist two stable equilibrium states, or attractors, separated by an unstable threshold state. In such systems, the trajectory of the system converges to one of the stable states depending on initial conditions, and it persists there unless subjected to a sufficiently large perturbation that drives it across the threshold to the other stable state.^[1]^[6] A key characteristic of bistable systems is their representation in terms of a potential energy landscape featuring two minima corresponding to the stable states, separated by a potential barrier at the unstable threshold. Transitioning between these states requires overcoming this barrier, which demands a specific amount of activation energy provided by external perturbations; without it, the system remains trapped in its current minimum due to the inherent stability. This behavior is illustrated in everyday devices, such as a light switch, which snaps between an "on" and "off" position and holds each until manually toggled, or a simple mechanical toggle that flips irreversibly between two positions upon sufficient force.^[7]^[8]^[9] To understand bistability, it is helpful to contrast it with monostable systems, which possess only a single stable equilibrium and thus always return to that state regardless of perturbations, and multistable systems, which feature more than two stable equilibria allowing for multiple persistent outcomes. Bistability emerges as a fundamental aspect of nonlinear dynamics, where nonlinear interactions enable the coexistence of multiple attractors and the sensitivity to initial conditions or perturbations.^[10]^[11] One consequence of bistability is hysteresis, wherein the system's response depends on its history, requiring different perturbation thresholds to switch states depending on the direction of change. Additionally, positive feedback loops often underlie bistable behavior by amplifying small deviations and reinforcing the selected state.^[12]^[13]

Historical Development

The concept of bistability emerged in the early 20th century through observations in mechanical and electrical systems, where systems could maintain two distinct stable states. One of the earliest documented examples came from electrical engineering, with snap-action switches designed to provide reliable toggling between on and off positions; the quick-break mechanism in light switches, invented by John Henry Holmes in 1884, laid groundwork for such behavior by enabling abrupt state changes to prevent arcing. More explicitly, in 1922, Balthasar van der Pol identified hysteresis—a hallmark of bistability—in nonlinear electric oscillators, marking an initial recognition of the phenomenon in dynamical systems.^[14]^[6] Theoretical insights into bistability deepened in the mid-20th century with advances in nonlinear dynamics, as researchers began modeling systems capable of multiple equilibria using differential equations. The development of electronic computers in the 1950s and 1960s enabled numerical simulations of nonlinear phenomena, revealing bistability in contexts like feedback loops and phase transitions. By the 1970s, this framework extended to chemical systems, particularly with the Belousov-Zhabotinsky (BZ) reaction, where oscillations and bistability were quantitatively analyzed; experiments by Anatol Zhabotinsky and colleagues in 1970 demonstrated excitable waves and dual stable states in this oscillatory reaction, highlighting bistability's role in far-from-equilibrium chemistry.^[15]^[16]^[17] In neurobiology, bistability gained prominence through the 1981 Morris-Lecar model, a simplified two-dimensional framework for excitable cells like barnacle muscle fibers, which exhibited bistable regimes between resting and spiking states under varying parameters. This model provided a tractable tool for analyzing neuronal dynamics, influencing subsequent studies on excitability. A pivotal milestone occurred in 2000 with the synthetic genetic toggle switch engineered by Timothy Gardner, Charles Cantor, and James Collins in Escherichia coli, demonstrating bistable gene regulation via mutual repression and enabling programmable cellular memory.90433-2)^[18] Post-2000, bistability evolved into an interdisciplinary cornerstone, shifting from physics and engineering toward biology and synthetic biology, where the toggle switch inspired circuits for gene expression control and biosensors. This era saw explosive growth in applications, fueled by genetic engineering tools like CRISPR. In parallel, post-2020 advancements extended bistability to quantum regimes; for instance, 2022 experiments with a single transmon qubit coupled to a tunable superconducting cavity demonstrated emergent macroscopic bistability, opening avenues for quantum information processing.^[19]^[20]

Mathematical Foundations

Dynamical Systems Models

Bistable systems are commonly modeled using first-order ordinary differential equations (ODEs) of the form \frac{dy}{dt} = f(y), where f(y) is a nonlinear function featuring three equilibria: two stable and one unstable. A canonical example is \frac{dy}{dt} = y - y^3, which exhibits stable equilibria at y = \pm 1 and an unstable equilibrium at y = 0. These equilibria are found by setting f(y) = 0, yielding y(y^2 - 1) = 0, and stability is confirmed by the sign of f'(y) at each point: f'(y) = 1 - 3y^2 < 0 at y = \pm 1 (attracting) and > 0 at y = 0 (repelling). Such ODE models can be derived from potential functions, where V(y) = -\int f(y) \, dy. For the example \frac{dy}{dt} = y - y^3, integration gives V(y) = -\frac{y^2}{2} + \frac{y^4}{4} + C, a double-well potential with minima at y = \pm 1 (stable states) and a maximum at y = 0 (unstable barrier). This formulation interprets the dynamics as motion downhill in the potential landscape, capturing the energetic basis for bistability in conservative systems. In the potential energy framework, bistable systems are represented as gradient flows \frac{dy}{dt} = -\frac{dV}{dy}, where V(y) possesses two local minima separated by a local maximum. Bistability arises from nonlinearities in V(y), typically cubic terms in the flow equation (e.g., f(y) = ry - y^3 for parameter r > 0) or quintic terms for more complex wells (e.g., incorporating higher-order corrections like -y^5 to model asymmetric or multi-barrier potentials). These nonlinearities ensure V(y) \to +\infty as |y| \to \infty, confining trajectories to one of the wells based on initial conditions. Gradient flows guarantee no periodic orbits, with all trajectories converging monotonically to equilibria.^[21] Phase plane analysis for these one-dimensional systems reduces to a phase line portrait, where the state space is the real line with arrows indicating the direction of flow based on the sign of f(y). Trajectories converge to the stable attractors at the potential minima, while diverging from the unstable point; the separatrix is the unstable equilibrium itself, dividing the line into basins of attraction for the two stable states. For \frac{dy}{dt} = y - y^3, flows point toward y = -1 for y < -1 or -1 < y < 0, away from y = 0 toward y = \pm 1, and toward y = 1 for y > 1, illustrating the threshold behavior at the separatrix.

Bifurcations and Stability Analysis

Bistability in dynamical systems often emerges through bifurcations where the number and stability of equilibria change as parameters vary, creating regions of parameter space where two stable states coexist. The saddle-node bifurcation is a primary mechanism for the creation and annihilation of stable and unstable equilibria, leading to bistability in non-symmetric systems. In this bifurcation, as a parameter (e.g., a control variable like stimulus strength) increases, a stable equilibrium and an adjacent unstable equilibrium collide and disappear, leaving only the other stable state; the reverse occurs when decreasing the parameter, resulting in a parameter interval of coexistence between two stable states. This process is irreversible without external perturbation once the bifurcation is crossed, as the lost state cannot be recovered by infinitesimal parameter changes.^[22] Another key bifurcation leading to bistability is the subcritical pitchfork, particularly in systems with symmetry, where it breaks the symmetry of a single stable equilibrium into two stable asymmetric states separated by an unstable one. Unlike the supercritical pitchfork, the subcritical variant produces unstable branches that extend into the pre-bifurcation regime, creating a hysteresis region where bistability persists over a range of parameters; this symmetry-breaking allows for alternative stable outcomes, such as distinct cell fates in biological contexts. Parameter sweeps reveal the coexistence region bounded by the subcritical pitchfork point and saddle-node folds on the imperfect branches, highlighting the bistable domain. Stability analysis of bistable equilibria relies on linearization around fixed points of ordinary differential equation (ODE) models, where the Jacobian matrix is evaluated at each equilibrium to determine local stability via its eigenvalues. For a stable equilibrium, all eigenvalues of the Jacobian must have negative real parts, ensuring perturbations decay exponentially; in bistable systems, the two stable states satisfy this, while the separating saddle (unstable equilibrium) has at least one positive real eigenvalue. Global stability is assessed using Lyapunov functions, which confirm asymptotic stability of attractors by showing a decrease along trajectories, though computing basin of attraction sizes requires additional techniques like estimating separatrices or simulating initial condition ensembles to quantify the volume or measure of initial states leading to each attractor.^[23] Bifurcation diagrams visually depict these dynamics by plotting equilibria as functions of a varying parameter, illustrating stability changes and coexistence regions; for instance, in the pitchfork model \frac{dx}{dt} = r x - x^3, the bifurcation at r = 0 shows the central equilibrium losing stability as two symmetric stable branches emerge for r > 0, marking the onset of bistability. Tools like XPPAUT, developed by G. Bard Ermentrout in the 1990s as an evolution of PHASEPLANE, facilitate such analysis by integrating numerical continuation (via AUTO) to compute and plot bifurcation diagrams, eigenvalues, and nullclines for ODE systems.^[24]^[25]

Physical and Engineering Applications

Mechanical and Structural Systems

Bistability in mechanical and structural systems arises from designs that leverage elastic instabilities to achieve two stable equilibrium configurations, enabling reliable switching with minimal energy input. Over-center mechanisms, a classic implementation, involve linkages or beams that pass through an unstable equilibrium point during transition, resulting in snap-through buckling. This behavior is exemplified in everyday devices such as the click mechanism of a ballpoint pen, where a prestressed spring drives the tip between extended and retracted states via buckling of a slender beam segment.^[26] Similarly, toggle clamps utilize over-center linkages to lock workpieces securely, with the mechanism snapping into a high-force holding position once the toggle point is surpassed.^[27] Circuit breakers employ analogous bistable toggles to maintain open or closed states, ensuring rapid disconnection under fault conditions without continuous actuation.^[28] In structural applications, bistable shells and membranes exploit geometric nonlinearity for compact storage and self-deployment, particularly in aerospace engineering. For instance, bistable tape-spring booms serve as lightweight supports for deployable antennas, curling into a compact roll in one stable state and extending rigidly in the other due to residual stresses from manufacturing.^[29] These structures enable efficient packaging of large apertures, such as satellite reflectors, by reversing buckling instabilities. Additionally, elastic instability in bistable configurations facilitates energy storage, where deformation stores potential energy in the higher state, released rapidly during snap-through; this principle enhances impact absorption in protective structures. Design principles for these systems emphasize prestressed elements and compliant mechanisms to induce bistability without rigid joints, reducing wear and enabling monolithic fabrication. Prestressed springs, often integrated as buckled beams, create the dual energy minima by imposing initial compressive loads that define the stable geometries.^[30] Compliant mechanisms achieve this through flexible hinges formed by thinned sections, allowing large deflections while maintaining structural integrity. Key quantitative metrics include the switching force, typically 1-10 N for macroscale over-center devices like clamps, which must overcome the energy barrier—the potential energy maximum between states, often 0.1-1 J in engineering prototypes—to initiate transition.^[31] Load-displacement curves exhibit characteristic hysteresis, reflecting the path-dependent switching.^[27]

Electronic and Optical Systems

In electronic circuits, bistability is achieved through positive feedback mechanisms that create two stable operating states, enabling reliable switching and memory functions. The Schmitt trigger, a foundational bistable element, operates as a comparator with hysteresis, where the output voltage feeds back to the input to define upper and lower thresholds, preventing noise-induced oscillations.^[32] This design, relying on operational amplifiers or transistor configurations, ensures clean transitions between high and low states, making it essential for signal conditioning in digital systems. Flip-flops, such as the SR latch, exemplify bistability via cross-coupled logic gates—typically NOR or NAND—that maintain one of two states (set or reset) until an input pulse alters it.^[33] The positive feedback loop in these inverters reinforces the state, providing the core for sequential logic. These bistable circuits underpin digital memory applications, notably in static random-access memory (SRAM) cells, where a 6T configuration uses two cross-coupled inverters to store a bit as one of two stable voltage levels.^[34] The inverters' feedback ensures non-volatility during read/write operations, with access transistors enabling bit-line interaction while preserving stability against leakage and noise. This bistability allows SRAM to achieve high-speed, low-power data retention in processors and caches, contrasting with dynamic alternatives by avoiding refresh cycles. Optical bistability emerges in photonic systems through nonlinear interactions in optical cavities, where the medium's refractive index or absorption depends on light intensity, leading to multiple steady-state transmission outputs for a given input. In dispersive bistability, a Fabry-Pérot cavity filled with a Kerr nonlinear medium exhibits this behavior, as the intensity-dependent phase shift creates feedback akin to electronic loops. Absorption bistability occurs in semiconductor etalons, where saturable absorption under resonant pumping allows switching between low- and high-transmission states. The steady-state relation in such models is given by the normalized intracavity field amplitude x satisfying

x = \frac{y}{1 + i(\phi_0 + C |x|^2)},

where y is the input field amplitude (Y = |y|^2), I = |x|^2 is the intracavity intensity, \phi_0 is the initial detuning, and C the cooperation parameter quantifying nonlinearity strength; the imaginary unit i accounts for phase dynamics. Post-2020 advancements have integrated quantum optical bistability into photonic chips, enabling compact, low-loss devices for all-optical computing. A theoretical study in 2023 proposed single-photon bistability in micron-scale Fabry-Pérot cavities with Kerr media, showing potential quantum-level switching thresholds below 1 photon for use in scalable quantum networks.^[35] These integrated platforms, fabricated on silicon or III-V semiconductors, facilitate all-optical switches and logic gates by exploiting cavity-enhanced nonlinearities, reducing power needs compared to bulk optics and paving the way for energy-efficient photonic processors.

Biological and Chemical Applications

Cellular and Molecular Biology

In cellular and molecular biology, bistability manifests through gene regulatory networks that incorporate positive feedback loops, enabling switch-like transitions between distinct gene expression states. These loops often involve transcription factors that autoregulate or mutually reinforce expression, allowing cells to maintain stable "on" or "off" phenotypes despite fluctuating inputs. A canonical natural example is the lac operon in Escherichia coli, where bistability arises under specific induction conditions, such as growth on lactose plus glucose or with gratuitous inducers like TMG, due to positive feedback involving permease-mediated uptake of inducer, which relieves repression by the lac repressor and amplifies initial low-level induction.^[36] Synthetic biology has recapitulated and engineered such bistability, as demonstrated by the genetic toggle switch constructed in E. coli using mutually repressive promoters driving lacI and tetR genes, which exhibits robust switching between two stable states controllable by chemical inducers.^[37]^[38] Bistability plays a pivotal role in cellular processes requiring decisive fate choices, such as differentiation and programmed cell death. In immune cell differentiation, positive feedback in CD4+ T helper cell polarization creates bistable switches that drive heterogeneous commitment to subsets like Th1 or Th2, governed by mutual inhibition between master regulators T-bet and GATA3, ensuring population-level diversity in responses to pathogens. Similarly, in apoptosis, the caspase activation cascade exhibits bistability through positive feedback where active caspase-3 amplifies its own production via cleavage of upstream pro-caspases, leading to an all-or-none commitment to cell death that protects against partial execution. This switch-like behavior can be modeled by equations incorporating ultrasensitive positive feedback, such as

\frac{dx}{dt} = r + \frac{x^5}{1 + x^5} - x,

where x represents the activator concentration, r is an external input, and the Hill term with coefficient 5 captures cooperative ultrasensitivity, yielding two stable steady states for intermediate r values that enable irreversible transitions.^[39]^[40] Physiologically, bistability contributes to developmental patterning and immune homeostasis by generating robust, heritable cell states amid variability. In embryonic development, the Sonic hedgehog (Shh) signaling pathway acts as a bistable genetic switch, where Gli transcription factors form autoregulatory loops that interpret graded Shh morphogen signals into discrete ventral neural tube identities, such as motor neurons versus interneurons. In immunity, bistable gene expression underlies bimodal population distributions observed in single-cell analyses of immune cells, where key response genes like those for cytokine production show two distinct expression modes across cells, reflecting stable polarization states influenced by single-cell variability and enabling adaptive heterogeneity in populations facing infections.^[41]^[42]

Chemical Reaction Networks

Bistability in chemical reaction networks arises primarily from autocatalytic mechanisms, where reaction products catalyze their own formation, creating positive feedback loops that can sustain two stable steady states. These mechanisms enable the system to switch between states depending on initial conditions or external parameters, often in open systems maintained far from equilibrium by continuous inflow and outflow. A prominent example is the Belousov-Zhabotinsky (BZ) reaction, an oscillatory system involving the oxidation of malonic acid by bromate in the presence of a metal catalyst like cerium or ruthenium, which exhibits bistability under certain conditions such as varying flow rates or stirring, allowing coexistence of oxidized and reduced states.^[43] In non-enzymatic contexts, similar positive feedback occurs in simple autocatalytic schemes, while in enzyme-substrate systems with product inhibition, the product can bind to the enzyme and suppress further catalysis, leading to bistable steady states where low or high substrate concentrations are stabilized.^[44] Theoretical models capture these dynamics through rate equations that reveal multiple steady states. The Schlögl model, a paradigmatic example of chemical bistability, consists of four reactions: A + 2X \rightleftharpoons 3X and B + X \rightleftharpoons C + 2X, where X is the autocatalyst, leading to a cubic rate equation \frac{dx}{dt} = k_1 a x^2 - k_2 x^3 + k_3 b - k_4 c x that supports two stable steady states separated by an unstable one for appropriate parameter values, illustrating how nonlinearity drives the transition.^[45] Another foundational model involves quadratic autocatalysis with non-linear decay, where bistability arises from the quadratic production term \alpha \beta (with \beta the autocatalyst) and inhibited decay \frac{\kappa_2 \beta}{1 + \rho \beta}, yielding multiple steady states in a continuous stirred-tank reactor under suitable flow and inhibition parameters. This highlights the role of non-linear decay in generating the S-shaped nullcline essential for bistability.^[46] Experimental realizations of bistability in chemical networks include pH-driven systems, such as the chlorite-thiosulfate reaction in a continuous stirred-tank reactor (CSTR), where autocatalytic production of H⁺ ions creates two stable pH regimes—one acidic and one basic—exhibiting hysteresis as pH oscillates or switches based on flow rates and initial conditions. These bistable behaviors find applications in chemical sensors, where the sharp switching in BZ-based systems detects analytes like metal ions by altering oscillation periods or state transitions, providing amplified signal responses.^[47] Additionally, bistable fronts in reaction-diffusion systems enable pattern formation, as seen in experiments where interacting fronts in bistable media produce complex Turing-like patterns, such as spots or stripes, through the propagation and collision of stable interfaces.^[48]

Advanced Phenomena

Hysteresis and Switching Behavior

In bistable systems, hysteresis manifests as a path-dependent response where the system's output depends not only on the current input but also on its prior state, resulting in distinct branches of behavior during forward and reverse sweeps of a control parameter. This phenomenon is graphically represented by hysteresis loops superimposed on the S-shaped steady-state curve characteristic of bistability, where the upper and lower branches correspond to stable states separated by an unstable middle branch; as the input parameter is increased or decreased, the system follows different paths, creating a closed loop that encloses an area proportional to the energy dissipated during the cycle.^[49] Switching in these systems occurs deterministically when the input exceeds a critical threshold, enabling the system to overcome the energy barrier separating the two stable states and transition irreversibly to the other state. In ferromagnetic materials, for instance, this flip is driven by the motion of domain walls under an applied magnetic field, where the critical point corresponds to the depinning of the wall from pinning sites, allowing rapid reconfiguration of the magnetization direction. Such mechanisms underpin applications in memory devices, where the bistable states enable non-volatile storage of binary information, and in sensors, where hysteresis provides sensitivity to threshold crossings for detecting environmental changes.^[50]^[51]^[52]^[53] The behavior of hysteresis can be quantified using analogs to magnetic parameters, such as coercivity—the minimum input magnitude required to induce switching between states—and remanence—the persistent output level after the input is removed to zero, reflecting the memory effect of the prior state. Recent post-2020 studies have explored ultrafast switching in nanomaterials, including phase-change materials like RbMnFe-based compounds, which exhibit picosecond-scale transitions while maintaining hysteresis loops up to 75 K wide, enabling high-speed, thermally robust devices. These hysteresis regions emerge from saddle-node bifurcations in the system's parameter space, as seen in simple mechanical toggles or genetic switches.^[54]

Stochastic and Noisy Bistability

In bistable systems, stochastic modeling incorporates random fluctuations to describe how noise perturbs the deterministic dynamics, leading to probabilistic transitions between stable states. A common approach is the Langevin equation, which adds a noise term to the deterministic evolution: \frac{dy}{dt} = f(y) + \sqrt{2D} \xi(t), where f(y) represents the deterministic force derived from a double-well potential, D is the noise intensity, and \xi(t) is Gaussian white noise with zero mean and unit variance.^[55] This formulation captures the continuous evolution of the system variable y under thermal or other fluctuating influences, enabling analysis of escape events from one potential well to the other.^[56] The probability density P(y, t) of the system's state evolves according to the Fokker-Planck equation, \frac{\partial P}{\partial t} = -\frac{\partial}{\partial y} [f(y) P] + D \frac{\partial^2 P}{\partial y^2}, which provides a diffusion-based description of the state distribution over time.^[55] In bistable potentials, this equation reveals how noise spreads the probability across the wells, with steady-state solutions often exhibiting two peaks corresponding to the stable states.^[56] Noise-induced phenomena in these systems include probabilistic switching, quantified by the Kramers' escape rate, which estimates the mean time \tau for a particle to surmount the potential barrier: \tau \approx \frac{2\pi}{\sqrt{|V''(min) V''(max)|}} e^{\Delta V / D}, where V''(min) and V''(max) are the curvatures at the minimum and maximum of the potential V(y), and \Delta V is the barrier height.^[57] This rate highlights the exponential sensitivity to noise strength D, making transitions rare for low noise but inevitable over long times. Additionally, noise can induce bimodality in the stationary probability distribution, where the density shows two distinct modes even if the deterministic system is monostable under certain parameter regimes, arising from multiplicative or state-dependent fluctuations.^[58] In biological contexts, stochastic bistability contributes to gene expression noise by amplifying fluctuations in protein levels through resource competition, resulting in bimodal distributions and switching between high- and low-expression states in genetic circuits.^[59] Recent research from 2023 to 2025 has explored quantum noise effects in systems like cat qubits, where biased bit-flip noise is leveraged for fault-tolerant quantum computing.^[60] However, bistability faces limitations in small systems like single molecules or bacterial cells, where low molecular counts and diffusion constraints make the phenomenon fragile, requiring precise volume and parameter tuning to sustain stable states against overwhelming noise.^[61]

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Bistability analyses of a caspase activation model for receptor ...
Apoptosis is an important physiological process crucially involved in development and homeostasis of multicellular organisms. Although the major signaling ...
[41]
The sonic hedgehog signaling system as a bistable genetic switch
The Shh network functions as a genetic switch, and we have theoretically and computationally analyzed how its structure can endow it with the ability to switch ...
[42]
Single-cell transcriptomics reveals bimodality in expression and ...
May 19, 2013 · We find extensive, and previously unobserved, bimodal variation in mRNA abundance and splicing patterns, which we validate by RNA-fluorescence ...
[43]
Stirring Effect on the Bistability of the Belousov−Zhabotinsky ...
Experiments show that the hysteresis of the bistable Belousov−Zhabotinsky reaction contracts along the directions of both the control parameter and the response ...
[44]
Understanding bistability in complex enzyme-driven reaction networks
Bistability is often associated with the presence of a pathway in which the product of one reaction either inhibits or promotes occurrence of another reaction, ...
[45]
Chemical reaction models for non-equilibrium phase transitions
Chemical reaction models for non-equilibrium phase transitions. Published: April 1972. Volume 253, pages 147–161, (1972); Cite this ...Missing: original paper
[46]
Quadratic autocatalysis with non-linear decay. II: the effect of ...
Aug 16, 2019 · In this section we provide the model equations for a chemical process governed by quadratic autocatalytic kinetics with catalyst decay subject ...
[47]
Sensing the distance to a source of periodic oscillations in a ...
Oct 3, 2005 · ... Belousov-Zhabotinsky reaction ... Therefore the described chemical sensor of distance requires a method of adaptation to the conditions it ...
[48]
Pattern Formation by Interacting Chemical Fronts - Science
Experiments on a bistable chemical reaction in a continuously fed thin gel layer reveal a new type of spatiotemporal pattern, one in which fronts propagate ...
[49]
Extracting and stabilizing the unstable states of hysteresis loops
Usually, we get an S-shaped solution curve (i.e. hysteresis loop) in a bistable system, where the upper and lower branches are stable and the intermediate ...
[50]
Magnetic bit stability: Competition between domain-wall and ...
To study the energy barrier for thermally induced switching, we develop a variational procedure to force the bit to traverse a smooth path through configuration ...
[51]
[PDF] Central role of domain wall depinning for perpendicular ... - arXiv
Domain-wall depinning by spin Hall torque, driven by in-plane current and a magnetic field, is the rate-limiting step for magnetic reversal.
[52]
To Be or Not to Be – Review of Electrical Bistability Mechanisms in ...
Feb 8, 2022 · This review traces the development in the organic memory device and discusses the various problems that continue to plague the field.
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Study of bistable behaviour in interacting Fe-based microwires by ...
Aug 15, 2020 · A bistable microwire was considered as an example of the magnetic hysteron at FORC diagrams. •. The CPM of hysteresis was treated for the ...
[54]
Ultrafast and persistent photoinduced phase transition at room ...
Jan 24, 2024 · Such ultrafast photoinduced phase transitions induced by a single laser pulse are very promising for optically-driven devices, memories, or ...
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Bistable systems: Master equation versus Fokker-Planck modeling
Jan 1, 1984 · A new Fokker-Planck modeling is presented which is superior to the conventional method based on the truncated Kramers-Moyal expansion.
[56]
[PDF] Bistable systems: Master equation versus Fokker-Planck modeling
1-3 Most of the analysis has been based on Fokker-Planck equations or stochastically equivalent Langevin equations. On the other hand, it has been pointed out ...
[57]
On the theory of activation: Kramers' reaction rate in bistable systems
Using Rayleigh's identity for the pertinent eigenvalue, the escape rate is obtained for a bistable system with a smooth parabolic barrier.
[58]
Noise-induced bistability in a simple mutual inhibition system
Aug 7, 2023 · In this study, we study noise-induced bistability in a simple bivariate mutual inhibition system with slow fluctuating responses to external ...Abstract · Article Text · INTRODUCTION · DISCUSSION
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Resource competition-driven bistability and stochastic switching ...
Apr 23, 2025 · We found that resource competition amplifies gene expression noise by introducing unexpected bistability and stochastic switching between the two stable states.
[60]
Scalable noisy quantum circuits for biased-noise qubits - Nature
Aug 26, 2025 · In this work, we consider biased-noise qubits affected only by bit-flip errors, which is motivated by existing systems of stabilized cat ...
[61]
Bistability: Requirements on Cell-Volume, Protein Diffusion, and ...
Bistability is considered wide-spread among bacteria and eukaryotic cells, useful e.g. for enzyme induction, bet hedging, and epigenetic switching.