arXiv subjects

F. Paul Spitzner

Publications and source records attributed to F. Paul Spitzner.

7 recordsLinked to original sources

arXiv2024

Signatures of hierarchical temporal processing in the mouse visual system

A core challenge for the brain is to process information across various timescales. This could be achieved by a hierarchical organization of temporal processing through intrinsic mechanisms (e.g., recurrent coupling or adaptation), but recent evidence from spike recordings of the rodent visual system seems to conflict with this hypothesis. Here, we used an optimized information-theoretic and classical autocorrelation analysis to show that information- and intrinsic timescales of spiking activity increase along the anatomical hierarchy of the mouse visual system, while information-theoretic predictability decreases. Moreover, the timescale hierarchy was invariant to the stimulus condition, whereas the decrease in predictability was strongest under natural movie stimulation. We could reproduce this effect in a basic recurrent network model with correlated sensory input. Our findings suggest that the rodent visual system indeed employs intrinsic mechanisms to achieve longer integration for higher cortical areas, while simultaneously reducing predictability for an efficient neural code.

q-bio.NC↗

arXiv2023

How contact patterns destabilize and modulate epidemic outbreaks

The spread of a contagious disease clearly depends on when infected individuals come into contact with susceptible ones. Such effects, however, have remained largely unexplored in the study of epidemic outbreaks. In particular, it remains unclear how the timing of contacts interacts with the latent and infectious stages of the disease. Here, we use real-world physical proximity data to study this interaction and find that the temporal statistics of actual human contact patterns i) destabilize epidemic outbreaks and ii) modulate the basic reproduction number. We explain both observations by distinct aspects of the observed contact patterns. On the one hand, we find the destabilization of outbreaks to be caused by temporal clustering of contacts leading to over-dispersed offspring distributions and increased probabilities of otherwise rare events (zero- and super-spreading). Notably, our analysis enables us to disentangle previously elusive sources of over-dispersion in empirical offspring distributions. On the other hand, we find the modulation of R0 to be caused by a periodically varying contact rate. Both mechanisms are a direct consequence of the memory in contact behavior, and we showcase a generative process that reproduces these non-Markovian statistics. Our results point to the importance of including non-Markovian contact timings into studies of epidemic outbreaks.

physics.soc-ph↗

arXiv2022

Modular architecture facilitates noise-driven control of synchrony in neuronal networks

Brain functions require both segregated processing of information in specialized circuits, as well as integration across circuits to perform high-level information processing. One possible way to implement these seemingly opposing demands is by flexibly switching between synchronous and less synchronous states. Understanding how complex synchronization patterns are controlled by the interaction of network architecture and external perturbations is thus a central challenge in neuroscience, but the mechanisms behind such interactions remain elusive. Here, we utilise precision neuroengineering to manipulate cultured neuronal networks and show that a modular architecture facilitates desynchronization upon asynchronous stimulation, making external noise a control parameter of synchrony. Using spiking neuron models, we then demonstrate that external noise can reduce the level of available synaptic resources, which make intermodular interactions more stochastic and thereby facilitates the breakdown of synchrony. Finally, the phenomenology of stochastic intermodular interactions is formulated into a mesoscopic model that incorporates a state-dependent gating mechanism for signal propagation. Taken together, our results demonstrate a network mechanism by which asynchronous inputs tune the inherent dynamical state in structured networks of excitable units.

q-bio.NC↗

arXiv2022

Intrinsic timescales of spiking activity in humans during wakefulness and sleep

Information processing in the brain requires integration of information over time. Such an integration can be achieved if signals are maintained in the network activity for the required period, as quantified by the intrinsic timescale. While short timescales are considered beneficial for fast responses to stimuli, long timescales facilitate information storage and integration. We quantified intrinsic timescales from spiking activity in the medial temporal lobe of humans. We found extended and highly diverse timescales ranging from tens to hundreds of milliseconds, though with no evidence for differences between subareas. Notably, however, timescales differed between sleep stages and were longest during slow wave sleep. This supports the hypothesis that intrinsic timescales are a central mechanism to tune networks to the requirements of different tasks and cognitive states.

q-bio.NC↗

arXiv2021

Low case numbers enable long-term stable pandemic control without lockdowns

The traditional long-term solutions for epidemic control involve eradication or population immunity. Here, we analytically derive the existence of a third viable solution: a stable equilibrium at low case numbers, where test-trace-and-isolate policies partially compensate for local spreading events, and only moderate restrictions remain necessary. In this equilibrium, daily cases stabilize around ten new infections per million people or less. However, stability is endangered if restrictions are relaxed or case numbers grow too high. The latter destabilization marks a tipping point beyond which the spread self-accelerates. We show that a lockdown can reestablish control and that recurring lockdowns are not necessary given sustained, moderate contact reduction. We illustrate how this strategy profits from vaccination and helps mitigate variants of concern. This strategy reduces cumulative cases (and fatalities) 4x more than strategies that only avoid hospital collapse. In the long term, immunization, large-scale testing, and international coordination will further facilitate control.

q-bio.PE↗

arXiv2020

The challenges of containing SARS-CoV-2 via test-trace-and-isolate

Without a cure, vaccine, or proven long-term immunity against SARS-CoV-2, test-trace-and-isolate (TTI) strategies present a promising tool to contain its spread. For any TTI strategy, however, mitigation is challenged by pre- and asymptomatic transmission, TTI-avoiders, and undetected spreaders, who strongly contribute to hidden infection chains. Here, we studied a semi-analytical model and identified two tipping points between controlled and uncontrolled spread: (1) the behavior-driven reproduction number of the hidden chains becomes too large to be compensated by the TTI capabilities, and (2) the number of new infections exceeds the tracing capacity. Both trigger a self-accelerating spread. We investigated how these tipping points depend on challenges like limited cooperation, missing contacts, and imperfect isolation. Our model results suggest that TTI alone is insufficient to contain an otherwise unhindered spread of SARS-CoV-2, implying that complementary measures like social distancing and improved hygiene remain necessary.

q-bio.PE↗

arXiv2020

Inferring change points in the COVID-19 spreading reveals the effectiveness of interventions

As COVID-19 is rapidly spreading across the globe, short-term modeling forecasts provide time-critical information for decisions on containment and mitigation strategies. A main challenge for short-term forecasts is the assessment of key epidemiological parameters and how they change when first interventions show an effect. By combining an established epidemiological model with Bayesian inference, we analyze the time dependence of the effective growth rate of new infections. Focusing on the COVID-19 spread in Germany, we detect change points in the effective growth rate that correlate well with the times of publicly announced interventions. Thereby, we can quantify the effect of interventions, and we can incorporate the corresponding change points into forecasts of future scenarios and case numbers. Our code is freely available and can be readily adapted to any country or region.

q-bio.PE↗