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Ofer Feinerman

Publications and source records attributed to Ofer Feinerman.

17 recordsLinked to original sources

Maximal response to a mechanical leader at critical group size in ant collectives

It is widely recognized that biological collectives operate near criticality to amplify their capability of collective response. The peak in susceptibility near criticality renders these groups highly responsive to external stimuli. While this phenomenon has been recognized and supported by evidence from theory, a direct experimental demonstration has been elusive. To bridge this gap, here we record the response of a group of Paratrechina longicornis ants to external stimuli as they join efforts to carry food to their nest. Using a robotic system that mimics a transient leader, we apply tactile ant-scale forces and measure the group's response at sub, near, and supercritical regimes. Supported by theory and simulations, we provide direct experimental evidence to demonstrate that at critical group size, the collective response of the ants to an external force is maximally amplified.

physics.bio-ph

The 2024 Motile Active Matter Roadmap

Activity and autonomous motion are fundamental aspects of many living and engineering systems. Here, the scale of biological agents covers a wide range, from nanomotors, cytoskeleton, and cells, to insects, fish, birds, and people. Inspired by biological active systems, various types of autonomous synthetic nano- and micromachines have been designed, which provide the basis for multifunctional, highly responsive, intelligent active materials. A major challenge for understanding and designing active matter is their inherent non-equilibrium nature due to persistent energy consumption, which invalidates equilibrium concepts such as free energy, detailed balance, and time-reversal symmetry. Furthermore, interactions in ensembles of active agents are often non-additive and non-reciprocal. An important aspect of biological agents is their ability to sense the environment, process this information, and adjust their motion accordingly. It is an important goal for the engineering of micro-robotic systems to achieve similar functionality. With many fundamental properties of motile active matter now reasonably well understood and under control, the ground is prepared for the study of physical aspects and mechanisms of motion in complex environments, of the behavior of systems with new physical features like chirality, of the development of novel micromachines and microbots, of the emergent collective behavior and swarming of intelligent self-propelled particles, and of particular features of microbial systems. The vast complexity of phenomena and mechanisms involved in the self-organization and dynamics of motile active matter poses major challenges, which can only be addressed by a truly interdisciplinary effort involving scientists from biology, chemistry, ecology, engineering, mathematics, and physics.

cond-mat.soft

Synergy as the failure of distributivity

The concept of emergence, or synergy in its simplest form, is widely used but lacks a rigorous definition. Our work connects information and set theory to uncover the mathematical nature of synergy as the failure of distributivity. It resolves the persistent self-contradiction of information decomposition theory and reinstates it as a primary route toward a rigorous definition of emergence. Our results suggest that non-distributive variants of set theory may be used to describe emergent physical systems.

cs.IT

Connecting cooperative transport by ants with the physics of self-propelled particles

Paratrechina longicornis ants are known for their ability to cooperatively transport large food items. Previous studies have focused on the behavioral rules of individual ants and explained the efficient coordination using the coupled-carrier model. In contrast to this microscopic description, we instead treat the transported object as a single self-propelled particle characterized by its velocity magnitude and angle. We experimentally observe P. longicornis ants cooperatively transporting loads of varying radii. By analyzing the statistical features of the load's movement, we show that its salient properties are well captured by a set of Langevin equations describing a self-propelled particle. We relate the parameters of our macroscopic model to microscopic properties of the system. While the autocorrelation time of the velocity direction increases with group size, the autocorrelation time of the speed has a maximum at an intermediate group size. This corresponds to the critical slowdown close to the phase transition identified in the coupled-carrier model. Our findings illustrate that a self-propelled particle model can effectively characterize a system of interacting individuals.

physics.bio-ph

Echo chambers in the Ising model and implications on the mean magnetization

The echo-chamber effect is a common term in opinion dynamic modeling to describe how a person's opinion might be artificially enhanced as it is reflected back at her through social interactions. Here, we study the existence of this effect in statistical mechanics models, which are commonly used to study opinion dynamics. We show that the Ising model does not exhibit echo-chambers, but this result is a consequence of a special symmetry. We then distinguish between three types of models: (i) those with a strong echo-chamber symmetry, that have no echo-chambers at all; (ii) those with a weak echo-chamber symmetry that can exhibit echo-chambers but only if there are external fields in the system, and (iii) models without echo-chamber symmetry that generically have echo-chambers. We use these results to construct an efficient algorithm to efficiently and precisely calculate magnetization in arbitrary tree networks. Finally, We apply this algorithm to study two systems: phase transitions in the random field Ising model on a Bethe lattice and the influence optimization problem in social networks.

cond-mat.stat-mech

Individual crop loads provide local control for collective food intake in ant colonies

Nutritional regulation by ants emerges from a distributed process: food is collected by a small fraction of workers, stored within the crops of individuals, and spreads via local ant-to-ant interactions. The precise individual level underpinnings of this collective regulation have remained unclear mainly due to difficulties in measuring food within ants crops. Here we image fluorescent liquid food in individually tagged Camponotus sanctus ants, and track the real-time food flow from foragers to their gradually satiating colonies. We show how the feedback between colony satiation level and food inflow is mediated by individual crop loads; specifically, the crop loads of recipient ants control food flow rates, while those of foragers regulate the frequency of foraging trips. Interestingly, these effects do not rise from pure physical limitations of crop capacity. Our findings suggest that the emergence of food intake regulation does not require individual foragers to assess the global state of the colony.

q-bio.PE

Emergent oscillations assist obstacle negotiation during ant cooperative transport

Collective motion by animal groups is affected by internal interactions, external constraints and the influx of information. A quantitative understanding of how these different factors give rise to different modes of collective motion is, at present, lacking.} Here, we study how ants that cooperatively transport a large food item react to an obstacle blocking their path. Combining experiments with a statistical physics model of mechanically coupled active agents, we show that the constraint induces a deterministic collective oscillatory mode that facilitates obstacle circumvention. We provide direct experimental evidence, backed by theory, that this motion is an emergent group effect that does not require any behavioral changes at the individual level. We trace these relaxation oscillations to the interplay between two forces; informed ants pull the load towards the nest while uninformed ants contribute to the motion's persistence along the tangential direction. The model's predictions that oscillations appear above a critical system size, that the group can spontaneously transition into its ordered phase, and that the system can exhibit complete rotations are all verified experimentally. We expect that similar oscillatory modes emerge in collective motion scenarios where the structure of the environment imposes conflicts between individually held information and the group's tendency for cohesiveness.

physics.bio-ph

Limits for Rumor Spreading in stochastic populations

Biological systems can share and collectively process information to yield emergent effects, despite inherent noise in communication. While man-made systems often employ intricate structural solutions to overcome noise, the structure of many biological systems is more amorphous. It is not well understood how communication noise may affect the computational repertoire of such groups. To approach this question we consider the basic collective task of rumor spreading, in which information from few knowledgeable sources must reliably flow into the rest of the population. In order to study the effect of communication noise on the ability of groups that lack stable structures to efficiently solve this task, we consider a noisy version of the uniform PULL model. We prove a lower bound which implies that, in the presence of even moderate levels of noise that affect all facets of the communication, no scheme can significantly outperform the trivial one in which agents have to wait until directly interacting with the sources. Our results thus show an exponential separation between the uniform PUSH and PULL communication models in the presence of noise. Such separation may be interpreted as suggesting that, in order to achieve efficient rumor spreading, a system must exhibit either some degree of structural stability or, alternatively, some facet of the communication which is immune to noise. We corroborate our theoretical findings with a new analysis of experimental data regarding recruitment in Cataglyphis niger desert ants.

cs.MA

Collaborative search on the plane without communication

We generalize the classical cow-path problem [7, 14, 38, 39] into a question that is relevant for collective foraging in animal groups. Specifically, we consider a setting in which k identical (probabilistic) agents, initially placed at some central location, collectively search for a treasure in the two-dimensional plane. The treasure is placed at a target location by an adversary and the goal is to find it as fast as possible as a function of both k and D, where D is the distance between the central location and the target. This is biologically motivated by cooperative, central place foraging such as performed by ants around their nest. In this type of search there is a strong preference to locate nearby food sources before those that are further away. Our focus is on trying to find what can be achieved if communication is limited or altogether absent. Indeed, to avoid overlaps agents must be highly dispersed making communication difficult. Furthermore, if agents do not commence the search in synchrony then even initial communication is problematic. This holds, in particular, with respect to the question of whether the agents can communicate and conclude their total number, k. It turns out that the knowledge of k by the individual agents is crucial for performance. Indeed, it is a straightforward observation that the time required for finding the treasure is $Ω$(D + D 2 /k), and we show in this paper that this bound can be matched if the agents have knowledge of k up to some constant approximation. We present an almost tight bound for the competitive penalty that must be paid, in the running time, if agents have no information about k. Specifically, on the negative side, we show that in such a case, there is no algorithm whose competitiveness is O(log k). On the other hand, we show that for every constant $ε\textgreater{} 0$, there exists a rather simple uniform search algorithm which is $O( \log^{1+ε} k)$-competitive. In addition, we give a lower bound for the setting in which agents are given some estimation of k. As a special case, this lower bound implies that for any constant $ε\textgreater{} 0$, if each agent is given a (one-sided) $k^ε$-approximation to k, then the competitiveness is $Ω$(log k). Informally, our results imply that the agents can potentially perform well without any knowledge of their total number k, however, to further improve, they must be given a relatively good approximation of k. Finally, we propose a uniform algorithm that is both efficient and extremely simple suggesting its relevance for actual biological scenarios.

cs.DC

Individual versus collective cognition in social insects

The concerted responses of eusocial insects to environmental stimuli are often referred to as collective cognition on the level of the colony.To achieve collective cognitiona group can draw on two different sources: individual cognitionand the connectivity between individuals.Computation in neural-networks, for example,is attributedmore tosophisticated communication schemes than to the complexity of individual neurons. The case of social insects, however, can be expected to differ. This is since individual insects are cognitively capable units that are often able to process information that is directly relevant at the level of the colony.Furthermore, involved communication patterns seem difficult to implement in a group of insects since these lack clear network structure.This review discusses links between the cognition of an individual insect and that of the colony. We provide examples for collective cognition whose sources span the full spectrum between amplification of individual insect cognition and emergent group-level processes.

q-bio.NC

The ANTS problem

We introduce the Ants Nearby Treasure Search (ANTS) problem, which models natural cooperative foraging behavior such as that performed by ants around their nest. In this problem, k probabilistic agents, initially placed at a central location, collectively search for a treasure on the two-dimensional grid. The treasure is placed at a target location by an adversary and the agents' goal is to find it as fast as possible as a function of both k and D, where D is the (unknown) distance between the central location and the target. We concentrate on the case in which agents cannot communicate while searching. It is straightforward to see that the time until at least one agent finds the target is at least $Ω$(D + D 2 /k), even for very sophisticated agents, with unrestricted memory. Our algorithmic analysis aims at establishing connections between the time complexity and the initial knowledge held by agents (e.g., regarding their total number k), as they commence the search. We provide a range of both upper and lower bounds for the initial knowledge required for obtaining fast running time. For example, we prove that log log k + $Θ$(1) bits of initial information are both necessary and sufficient to obtain asymptotically optimal running time, i.e., O(D +D 2 /k). We also we prove that for every 0 \textless{} \textless{} 1, running in time O(log 1-- k $\times$(D +D 2 /k)) requires that agents have the capacity for storing $Ω$(log k) different states as they leave the nest to start the search. To the best of our knowledge, the lower bounds presented in this paper provide the first non-trivial lower bounds on the memory complexity of probabilistic agents in the context of search problems. We view this paper as a "proof of concept" for a new type of interdisciplinary methodology. To fully demonstrate this methodology, the theoretical tradeoff presented here (or a similar one) should be combined with measurements of the time performance of searching ants.

cs.DC

Fast Rendezvous on a Cycle by Agents with Different Speeds

The difference between the speed of the actions of different processes is typically considered as an obstacle that makes the achievement of cooperative goals more difficult. In this work, we aim to highlight potential benefits of such asynchrony phenomena to tasks involving symmetry breaking. Specifically, in this paper, identical (except for their speeds) mobile agents are placed at arbitrary locations on a cycle of length $n$ and use their speed difference in order to rendezvous fast. We normalize the speed of the slower agent to be 1, and fix the speed of the faster agent to be some $c>1$. (An agent does not know whether it is the slower agent or the faster one.) The straightforward distributed-race DR algorithm is the one in which both agents simply start walking until rendezvous is achieved. It is easy to show that, in the worst case, the rendezvous time of DR is $n/(c-1)$. Note that in the interesting case, where $c$ is very close to 1 this bound becomes huge. Our first result is a lower bound showing that, up to a multiplicative factor of 2, this bound is unavoidable, even in a model that allows agents to leave arbitrary marks, even assuming sense of direction, and even assuming $n$ and $c$ are known to agents. That is, we show that under such assumptions, the rendezvous time of any algorithm is at least $\frac{n}{2(c-1)}$ if $c\leq 3$ and slightly larger if $c>3$. We then construct an algorithm that precisely matches the lower bound for the case $c\leq 2$, and almost matches it when $c>2$. Moreover, our algorithm performs under weaker assumptions than those stated above, as it does not assume sense of direction, and it allows agents to leave only a single mark (a pebble) and only at the place where they start the execution. Finally, we investigate the setting in which no marks can be used at all, and show tight bounds for $c\leq 2$, and almost tight bounds for $c>2$.

cs.DC

Clock Synchronization and Distributed Estimation in Highly Dynamic Networks: An Information Theoretic Approach

We consider the External Clock Synchronization problem in dynamic sensor networks. Initially, sensors obtain inaccurate estimations of an external time reference and subsequently collaborate in order to synchronize their internal clocks with the external time. For simplicity, we adopt the drift-free assumption, where internal clocks are assumed to tick at the same pace. Hence, the problem is reduced to an estimation problem, in which the sensors need to estimate the initial external time. This work is further relevant to the problem of collective approximation of environmental values by biological groups. Unlike most works on clock synchronization that assume static networks, this paper focuses on an extreme case of highly dynamic networks. Specifically, we assume a non-adaptive scheduler adversary that dictates in advance an arbitrary, yet independent, meeting pattern. Such meeting patterns fit, for example, with short-time scenarios in highly dynamic settings, where each sensor interacts with only few other arbitrary sensors. We propose an extremely simple clock synchronization algorithm that is based on weighted averages, and prove that its performance on any given independent meeting pattern is highly competitive with that of the best possible algorithm, which operates without any resource or computational restrictions, and knows the meeting pattern in advance. In particular, when all distributions involved are Gaussian, the performances of our scheme coincide with the optimal performances. Our proofs rely on an extensive use of the concept of Fisher information. We use the Cramer-Rao bound and our definition of a Fisher Channel Capacity to quantify information flows and to obtain lower bounds on collective performance. This opens the door for further rigorous quantifications of information flows within collaborative sensors.

cs.DC

Breathe before Speaking: Efficient Information Dissemination Despite Noisy, Limited and Anonymous Communication

Distributed computing models typically assume reliable communication between processors. While such assumptions often hold for engineered networks, e.g., due to underlying error correction protocols, their relevance to biological systems, wherein messages are often distorted before reaching their destination, is quite limited. In this study we take a first step towards reducing this gap by rigorously analyzing a model of communication in large anonymous populations composed of simple agents which interact through short and highly unreliable messages. We focus on the broadcast problem and the majority-consensus problem. Both are fundamental information dissemination problems in distributed computing, in which the goal of agents is to converge to some prescribed desired opinion. We initiate the study of these problems in the presence of communication noise. Our model for communication is extremely weak and follows the push gossip communication paradigm: In each round each agent that wishes to send information delivers a message to a random anonymous agent. This communication is further restricted to contain only one bit (essentially representing an opinion). Lastly, the system is assumed to be so noisy that the bit in each message sent is flipped independently with probability $1/2-ε$, for some small $ε>0$. Even in this severely restricted, stochastic and noisy setting we give natural protocols that solve the noisy broadcast and the noisy majority-consensus problems efficiently. Our protocols run in $O(\log n / ε^2)$ rounds and use $O(n \log n / ε^2)$ messages/bits in total, where $n$ is the number of agents. These bounds are asymptotically optimal and, in fact, are as fast and message efficient as if each agent would have been simultaneously informed directly by an agent that knows the prescribed desired opinion.

cs.DC

Memory Lower Bounds for Randomized Collaborative Search and Applications to Biology

Initial knowledge regarding group size can be crucial for collective performance. We study this relation in the context of the {\em Ants Nearby Treasure Search (ANTS)} problem \cite{FKLS}, which models natural cooperative foraging behavior such as that performed by ants around their nest. In this problem, $k$ (probabilistic) agents, initially placed at some central location, collectively search for a treasure on the two-dimensional grid. The treasure is placed at a target location by an adversary and the goal is to find it as fast as possible as a function of both $k$ and $D$, where $D$ is the (unknown) distance between the central location and the target. It is easy to see that $T=Ω(D+D^2/k)$ time units are necessary for finding the treasure. Recently, it has been established that $O(T)$ time is sufficient if the agents know their total number $k$ (or a constant approximation of it), and enough memory bits are available at their disposal \cite{FKLS}. In this paper, we establish lower bounds on the agent memory size required for achieving certain running time performances. To the best our knowledge, these bounds are the first non-trivial lower bounds for the memory size of probabilistic searchers. For example, for every given positive constant $ε$, terminating the search by time $O(\log^{1-ε} k \cdot T)$ requires agents to use $Ω(\log\log k)$ memory bits. Such distributed computing bounds may provide a novel, strong tool for the investigation of complex biological systems.

cs.DC

The Physics of Living Neural Networks

Improvements in technique in conjunction with an evolution of the theoretical and conceptual approach to neuronal networks provide a new perspective on living neurons in culture. Organization and connectivity are being measured quantitatively along with other physical quantities such as information, and are being related to function. In this review we first discuss some of these advances, which enable elucidation of structural aspects. We then discuss two recent experimental models that yield some conceptual simplicity. A one-dimensional network enables precise quantitative comparison to analytic models, for example of propagation and information transport. A two-dimensional percolating network gives quantitative information on connectivity of cultured neurons. The physical quantities that emerge as essential characteristics of the network in vitro are propagation speeds, synaptic transmission, information creation and capacity. Potential application to neuronal devices is discussed.

cond-mat.dis-nn

String Theory on AdS_3 x S^3 x S^3 x S^1

Spacetime properties of superstrings on AdS_3 x S^3 x S^3 x S^1 are studied. The boundary theory is a two dimensional superconformal field theory with a large N=(4,4) supersymmetry.

hep-th