Recently we introduced the active Dyson Brownian motion model (DBM), in which N run-and-tumble particles interact via a logarithmic repulsive potential in the presence of a harmonic well. We found that in a broad range of parameters the density of particles converges at large N to the Wigner semicircle law as in the passive case. In this paper we provide an analytical support for this numerical observation by studying the fluctuations of the positions of the particles in the nonequilibrium stationary state of the active DBM in the regime of weak noise and large persistence time. In this limit we obtain an analytical expression for the covariance between the particle positions for any N from the exact inversion of the Hessian matrix of the system. We show that, when the number of particles is large N≫1, the covariance matrix takes scaling forms that we compute explicitly both in the bulk and at the edge of the support of the semicircle. In the bulk the covariance scales as N^{-1}, while at the edge it scales as N^{-2/3}. Remarkably we find that these results can be transposed directly to an equilibrium model, the overdamped Calogero-Moser model in the low-temperature limit, providing an analytical confirmation of the numerical results obtained by Agarwal et al. [J. Stat. Phys. 176, 1463 (2019)0022-471510.1007/s10955-019-02349-6]. For this model our method also allows us to obtain the equilibrium two-time correlations and their dynamical scaling forms both in the bulk and at the edge. Our predictions at the edge are reminiscent of a recent result in the mathematics literature in Gorin and Kleptsyn [arXiv:2009.02006 (2023)] on the (passive) DBM. That result can be recovered by the present methods and also, as we show, using the stochastic Airy operator. Finally, our analytical predictions are confirmed by precise numerical simulations in a wide range of parameters.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1103/PhysRevE.109.014136 | DOI Listing |
Antioxidants (Basel)
November 2024
Barts & The London Faculty of Medicine & Dentistry, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ, UK.
The majority of naturally occurring mutations of the human gene , are associated with reduced or completely absent xanthine oxidoreductase (XOR) activity, leading to a disease known as classical xanthinuria, which is due to the accumulation and excretion of xanthine in urine. Three types of classical xanthinuria have been identified: type I, characterised by XOR deficiency, type II, caused by XOR and aldehyde oxidase (AO) deficiency, and type III due to XOR, AO, and sulphite oxidase (SO) deficiency. Type I and II are considered rare autosomal recessive disorders, a condition where two copies of the mutated gene must be present to develop the disease or trait.
View Article and Find Full Text PDFCureus
November 2024
Medical Education, NHS Lothian, Edinburgh, GBR.
Introduction The incidence of malignant melanoma (MM) in the United Kingdom (UK) has significantly increased in recent years and is expected to continue to rise over the next decade. Despite the preventable nature of most MM cases, existing evidence suggests that public health education around skin cancer and sun safety is often suboptimal, particularly for secondary school populations. Unlike primary school curricula, there is no national guidance to mandate the teaching of this topic in secondary school.
View Article and Find Full Text PDFNano Lett
December 2024
Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory of Advanced Negative Carbon Technologies, Soochow University, Suzhou 215123, China.
MoS is a promising sulfur host material for lithium-sulfur (Li-S) batteries, but its low conductivity and limited active edge sites largely inhibit the catalytic activity toward the conversion of lithium polysulfides (LiPSs). Herein, we propose an electron bridge strategy by combining interlayer structure modification and electronic modulation to activate the basal-plane catalytic activity of MoS for the highly efficient catalytic conversion of LiPSs. As validated by experimental characterizations and theoretical calculations, the proposed strategy not only creates a conductive network but also induces delocalized electron redistribution within the MoS basal planes, leading to facilitated interfacial charge transfer kinetics and accelerated LiPSs redox kinetics.
View Article and Find Full Text PDFToxicol Appl Pharmacol
December 2024
CSL Ltd, Bio21 Institute, Victoria, Australia. Electronic address:
CSL040 is a soluble, recombinant fragment of the complement receptor 1 (CR1) extracellular domain that acts as an inhibitor of all three pathways of the complement system. Systemic toxicity, toxicokinetics (TK), and pharmacodynamics (PD) of CSL040 were assessed in two-week intravenous (IV) bolus studies in Han Wistar rats and cynomolgus monkeys. Recovery from any effects was evaluated during a four-week recovery period.
View Article and Find Full Text PDFChimia (Aarau)
November 2024
Extreme Environments Research Laboratory, École Polytechnique Féderale de Lausanne, CH-1951 Sion.
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!