On level line fluctuations of SOS surfaces above a wall

We study the low temperature $(2+1)$D Solid-On-Solid model on $[[1, L]]^2$ with zero boundary conditions and non-negative heights (a floor at height $0$). Caputo et al. (2016) established that this random surface typically admits either $\mathfrak h$ or $\mathfrak h+1$ many nested macroscopic level line loops $\{\mathcal L_i\}_{i\geq 0}$ for an explicit $\mathfrak h\asymp \log L$, and its top loop $\mathcal L_0$ has cube-root fluctuations: e.g., if $\rho(x)$ is the vertical displacement of $\mathcal L_0$ from the bottom boundary point $(x,0)$, then $\max \rho(x) = L^{1/3+o(1)}$ over $x\in I_0:=L/2+[[-L^{2/3},L^{2/3}]]$. It is believed that rescaling $\rho$ by $L^{1/3}$ and $I_0$ by $L^{2/3}$ would yield a limit law of a diffusion on $[-1,1]$. However, no nontrivial lower bound was known on $\rho(x)$ for a fixed $x\in I_0$ (e.g., $x=\frac L2$), let alone on $\min\rho(x)$ in $I_0$, to complement the bound on $\max\rho(x)$. Here we show a lower bound of the predicted order $L^{1/3}$: for every $\epsilon>0$ there exists $\delta>0$ such that $\min_{x\in I_0} \rho(x) \geq \delta L^{1/3}$ with probability at least $1-\epsilon$. The proof relies on the Ornstein--Zernike machinery due to Campanino--Ioffe--Velenik, and a result of Ioffe, Shlosman and Toninelli (2015) that rules out pinning in Ising polymers with modified interactions along the boundary. En route, we refine the latter result into a Brownian excursion limit law, which may be of independent interest.Comment: 48 pages, 2 figure

The extremal point process of branching Brownian motion in Rd\mathbb{R}^d

We consider a branching Brownian motion in $\mathbb{R}^d$ with $d \geq 1$ in which the position $X_t^{(u)}\in \mathbb{R}^d$ of a particle $u$ at time $t$ can be encoded by its direction $\theta^{(u)}_t \in \mathbb{S}^{d-1}$ and its distance $R^{(u)}_t$ to 0. We prove that the {\it extremal point process} $\sum \delta_{\theta^{(u)}_t, R^{(u)}_t - m_t^{(d)}}$ (where the sum is over all particles alive at time $t$ and $m^{(d)}_t$ is an explicit centring term) converges in distribution to a randomly shifted decorated Poisson point process on $\mathbb{S}^{d-1} \times \mathbb{R}$. More precisely, the so-called {\it clan-leaders} form a Cox process with intensity proportional to $D_\infty(\theta) e^{-\sqrt{2}r} ~\mathrm{d} r ~\mathrm{d} \theta$, where $D_\infty(\theta)$ is the limit of the derivative martingale in direction $\theta$ and the decorations are i.i.d. copies of the decoration process of the standard one-dimensional branching Brownian motion. This proves a conjecture of Stasi\'nski, Berestycki and Mallein (Ann. Inst. H. Poincar\'{e} 57:1786--1810, 2021), and builds on that paper and on Kim, Lubetzky and Zeitouni (arXiv:2104.07698).Comment: 20 pages, 4 figure

Trace Formulae and Spectral Statistics for Discrete Laplacians on Regular Graphs (I)

Trace formulae for d-regular graphs are derived and used to express the spectral density in terms of the periodic walks on the graphs under consideration. The trace formulae depend on a parameter w which can be tuned continuously to assign different weights to different periodic orbit contributions. At the special value w=1, the only periodic orbits which contribute are the non back- scattering orbits, and the smooth part in the trace formula coincides with the Kesten-McKay expression. As w deviates from unity, non vanishing weights are assigned to the periodic walks with back-scatter, and the smooth part is modified in a consistent way. The trace formulae presented here are the tools to be used in the second paper in this sequence, for showing the connection between the spectral properties of d-regular graphs and the theory of random matrices.Comment: 22 pages, 3 figure

Lower Bounds on the Time/Memory Tradeoff of Function Inversion

We study time/memory tradeoffs of function inversion: an algorithm, i.e., an inverter, equipped with an $s$-bit advice on a randomly chosen function $f\colon [n] \mapsto [n]$ and using $q$ oracle queries to $f$, tries to invert a randomly chosen output $y$ of $f$, i.e., to find $x\in f^{-1}(y)$. Much progress was done regarding adaptive function inversion - the inverter is allowed to make adaptive oracle queries. Hellman [IEEE transactions on Information Theory \u2780] presented an adaptive inverter that inverts with high probability a random $f$. Fiat and Naor [SICOMP \u2700] proved that for any $s,q$ with $s^3 q = n^3$ (ignoring low-order terms), an $s$-advice, $q$-query variant of Hellman\u27s algorithm inverts a constant fraction of the image points of any function. Yao [STOC \u2790] proved a lower bound of $sq\ge n$ for this problem. Closing the gap between the above lower and upper bounds is a long-standing open question. Very little is known for the non-adaptive variant of the question - the inverter chooses its queries in advance. The only known upper bounds, i.e., inverters, are the trivial ones (with $s+q= n$), and the only lower bound is the above bound of Yao. In a recent work, Corrigan-Gibbs and Kogan [TCC \u2719] partially justified the difficulty of finding lower bounds on non-adaptive inverters, showing that a lower bound on the time/memory tradeoff of non-adaptive inverters implies a lower bound on low-depth Boolean circuits. Bounds that, for a strong enough choice of parameters, are notoriously hard to prove. We make progress on the above intriguing question, both for the adaptive and the non-adaptive case, proving the following lower bounds on restricted families of inverters: - Linear-advice (adaptive inverter): If the advice string is a linear function of $f$ (e.g., $A\times f$, for some matrix $A$, viewing $f$ as a vector in $[n]^n$), then $s+q \in \Omega(n)$. The bound generalizes to the case where the advice string of $f_1 + f_2$, i.e., the coordinate-wise addition of the truth tables of $f_1$ and $f_2$, can be computed from the description of $f_1$ and $f_2$ by a low communication protocol. - Affine non-adaptive decoders: If the non-adaptive inverter has an affine decoder - it outputs a linear function, determined by the advice string and the element to invert, of the query answers - then $s \in \Omega(n)$ (regardless of $q$). - Affine non-adaptive decision trees: If the non-adaptive inversion algorithm is a $d$-depth affine decision tree - it outputs the evaluation of a decision tree whose nodes compute a linear function of the answers to the queries - and $q 0$, then $s\in \Omega(n/d \log n)$

Glauber Dynamics for the mean-field Potts Model

We study Glauber dynamics for the mean-field (Curie-Weiss) Potts model with $q\geq 3$ states and show that it undergoes a critical slowdown at an inverse-temperature $\beta_s(q)$ strictly lower than the critical $\beta_c(q)$ for uniqueness of the thermodynamic limit. The dynamical critical $\beta_s(q)$ is the spinodal point marking the onset of metastability. We prove that when $\beta<\beta_s(q)$ the mixing time is asymptotically $C(\beta, q) n \log n$ and the dynamics exhibits the cutoff phenomena, a sharp transition in mixing, with a window of order $n$. At $\beta=\beta_s(q)$ the dynamics no longer exhibits cutoff and its mixing obeys a power-law of order $n^{4/3}$. For $\beta>\beta_s(q)$ the mixing time is exponentially large in $n$. Furthermore, as $\beta \uparrow \beta_s$ with $n$, the mixing time interpolates smoothly from subcritical to critical behavior, with the latter reached at a scaling window of $O(n^{-2/3})$ around $\beta_s$. These results form the first complete analysis of mixing around the critical dynamical temperature --- including the critical power law --- for a model with a first order phase transition.Comment: 45 pages, 5 figure

The ProPrems trial: investigating the effects of probiotics on late onset sepsis in very preterm infants

BACKGROUND: Late onset sepsis is a frequent complication of prematurity associated with increased mortality and morbidity. The commensal bacteria of the gastrointestinal tract play a key role in the development of healthy immune responses. Healthy term infants acquire these commensal organisms rapidly after birth. However, colonisation in preterm infants is adversely affected by delivery mode, antibiotic treatment and the intensive care environment. Altered microbiota composition may lead to increased colonisation with pathogenic bacteria, poor immune development and susceptibility to sepsis in the preterm infant.Probiotics are live microorganisms, which when administered in adequate amounts confer health benefits on the host. Amongst numerous bacteriocidal and nutritional roles, they may also favourably modulate host immune responses in local and remote tissues. Meta-analyses of probiotic supplementation in preterm infants report a reduction in mortality and necrotising enterocolitis. Studies with sepsis as an outcome have reported mixed results to date.Allergic diseases are increasing in incidence in "westernised" countries. There is evidence that probiotics may reduce the incidence of these diseases by altering the intestinal microbiota to influence immune function. METHODS/DESIGN: This is a multi-centre, randomised, double blinded, placebo controlled trial investigating supplementing preterm infants born at < 32 weeks' gestation weighing < 1500 g, with a probiotic combination (Bifidobacterium infantis, Streptococcus thermophilus and Bifidobacterium lactis). A total of 1,100 subjects are being recruited in Australia and New Zealand. Infants commence the allocated intervention from soon after the start of feeds until discharge home or term corrected age. The primary outcome is the incidence of at least one episode of definite (blood culture positive) late onset sepsis before 40 weeks corrected age or discharge home. Secondary outcomes include: Necrotising enterocolitis, mortality, antibiotic usage, time to establish full enteral feeds, duration of hospital stay, growth measurements at 6 and 12 months' corrected age and evidence of atopic conditions at 12 months' corrected age. DISCUSSION: Results from previous studies on the use of probiotics to prevent diseases in preterm infants are promising. However, a large clinical trial is required to address outstanding issues regarding safety and efficacy in this vulnerable population. This study will address these important issues. TRIAL REGISTRATION: Australia and New Zealand Clinical Trials Register (ANZCTR): ACTRN012607000144415The product "ABC Dophilus Probiotic Powder for Infants®", Solgar, USA has its 3 probiotics strains registered with the Deutsche Sammlung von Mikroorganismen und Zellkulturen (DSMZ--German Collection of Microorganisms and Cell Cultures) as BB-12 15954, B-02 96579, Th-4 15957

The Scholar and the Future of the Research Library (Book Rerview)

published or submitted for publicatio

The maximum of branching Brownian motion in Rd\mathbb{R}^d

We show that in branching Brownian motion (BBM) in $\mathbb{R}^d$, $d\geq 2$, the law of $R_t^*$, the maximum distance of a particle from the origin at time $t$, converges as $t\to\infty$ to the law of a randomly shifted Gumbel random variable.Comment: 53 pages, 7 figures. Revision addresses referees comments and refers to the recent arXiv:2112.08407. To appear in the Annals of Applied Probabilit

The extremal point process of branching Brownian motion in Rd\mathbb R^d

International audienceWe consider a branching Brownian motion in $\mathbb R^d$ with $d \geq 1$ in which the position $X_t^{(u)}\in \mathbb R^d$ of a particle $u$ at time $t$ can be encoded by its direction $\theta^{(u)}_t \in \mathbb S^{d-1}$ and its distance $R^{(u)}_t$ to 0. We prove that the \emph{extremal point process} $\sum \delta_{\theta^{(u)}_t, R^{(u)}_t - m_t^{(d)}}$ (where the sum is over all particles alive at time $t$ and $m^{(d)}_t$ is an explicit centring term) converges in distribution to a randomly shifted decorated Poisson point process on $\mathbb S^{d-1} \times \mathbb R$. More precisely, the so-called {\it clan-leaders} form a Cox process with intensity proportional to $D_\infty(\theta) e^{-\sqrt{2}r} \mathrm d r\mathrm d \theta$, where $D_\infty(\theta)$ is the limit of the derivative martingale in direction $\theta$ and the decorations are i.i.d.\ copies of the decoration process of the standard one-dimensional branching Brownian motion.This proves a conjecture of Stasi\'nski, Berestycki and Mallein (Ann.\ Inst.\ H.\ Poincar\'{e} 57:1786--1810, 2021), and builds on that paper andon Kim, Lubetzky and Zeitouni (arXiv:2104.07698)