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Valentin Slepukhin

Publications and source records attributed to Valentin Slepukhin.

2 recordsLinked to original sources

Growth-Induced Transitions in Viscoelastic Matter

Growth is a fundamental process in living systems. Although the stress-deformation response of growing materials is often described as either purely elastic or purely viscous, many biological tissues, from biofilms to tumors, exhibit both elastic and viscous behavior. Here, we show that this viscoelastic response can crucially control the mechanics of proliferating matter when the growth rate becomes comparable to the rate of stress relaxation. Focusing first on the prototypical case of a growing elastic beam, we find that the dynamics are governed by a single dimensionless parameter, $g \tau$, where $g$ is the growth rate and $\tau$ is the viscoelastic relaxation time. While the limits $g \tau \to 0$ and $g \tau \to \infty$ recover purely viscous and purely elastic behavior, respectively, the intermediate regime is not merely a smooth crossover between them. Instead, qualitatively new dynamics emerge at $g \tau \sim 1$, including rapid transitions between metastable states that occur in neither limiting regime. We then develop a general, growth-compatible theoretical framework in which unconstrained growth is intrinsically stress-free, extending the analysis to other prototypical geometries and enabling simulations of more realistic growing biological materials. Within this framework, sharp mechanical transitions arise when stress generated by exponential growth accumulates faster than it can be dissipated by viscoelastic relaxation.

cond-mat.soft

Barrier-Free Microhabitats: Self-Organized Seclusion in Microbial Communities

Bacteria frequently colonize natural microcavities such as gut crypts, plant apoplasts, and soil pores. Recent studies have shown that the physical structure of these spaces plays a crucial role in shaping the stability and resilience of microbial populations (Karita et al., PNAS 2022, Postek et al. PNAS 2024). Here, we demonstrate that protected microhabitats can emerge dynamically, even in the absence of physical barriers. Interactions with surface features -- such as roughness or friction -- lead microbial populations to self-organize into effectively segregated subpopulations. Our numerical and analytical models reveal that this self-organization persists even when strains have different growth rates, allowing slower-growing strains to avoid competitive exclusion. These findings suggest that emergent spatial structuring can serve as a fundamental mechanism for maintaining microbial diversity, despite selection pressures, competition, and genetic drift.

q-bio.PE