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  • Open Access

Distinguishing brain oscillations – understanding differences in topography, frequency, and incidence by a simple modeling framework

BMC Neuroscience200910 (Suppl 1) :P229

  • Published:


  • Sleep Spindle
  • Slow Oscillation
  • Gamma Oscillation
  • Neural Oscillator
  • Functional Entity

Brain oscillations such as alpha waves in relaxed wakefulness, sleep spindles and slow oscillations in sleep, or beta and gamma oscillations are important markers for the brain state and may also play functional roles in some cognitive processes. The different names indicate that they are considered as distinct entities, with frequency and topography being the features that distinguish the two. Sleep spindles in the human EEG, for instance, are oscillations in a frequency range between 11 and 16 Hz. They were shown to be related to the memory consolidating effects of sleep [1]. One often distinguishes between slow and fast spindles, which supposedly serve different functional purposes. Both types of spindles have not only different frequencies, but also different topographical distributions in the scalp EEG. The distinction between slow and fast sleep spindles in measured data is, however, by no means simple and uncontroversial. This is primarily due to the large amount of variation in the frequency of spindles, which not only vary across individuals but are also state-dependent (sleep stage and time in the night) [2]. Additionally, the delineation to other types of oscillations can be unclear – for instance between slow sleep spindles and frontal alpha oscillations. Similar problems occur for other brain oscillations, for instance in the analysis of delta and slow oscillations.

This situation poses a challenge to both data analysis and computational modeling. The present work continues our previous work [3] on combining data-analysis methods with computational modeling to improve the understanding of brain oscillations.

Our basic model is a two-dimensional noisy field of excitatory-inhibitory neural oscillators similar to the Wilson-Cowan equations but coupled over an adjustable lateral region. An additional oscillator can be coupled to the network either locally or globally mimicking thalamic driving. Artificial "EEG" signals are then produced as local averages of neural activity and oscillatory events are analysed using both a recently developed method based on fitting linear models to short segments in a sliding window fashion [2] and spectral analysis. The model is augmented by an additional slow hysteresis loop that can switch the local circuits between two operational states thus mimicking the cortical slow oscillation between up and down states. Systematic parameter inhomogeneities (gradients, blocks, random values) modulate the properties of local elements further.

We demonstrate that this model reveals oscillatory patterns at multiple frequencies beyond the single frequency mean field solution. Properties of the observed oscillations are investigated as functions of the model parameters. We discuss to which extent these findings reveal limitations on the view of brain oscillations as discrete physiological and functional entities, and consider possible implications.

Authors’ Affiliations

Max Planck Institute for Mathematics in the Sciences, D-04103 Leipzig, Germany
Centre for Theoretical and Computational Neuroscience, University of Plymouth, PL4 8AA Plymouth, UK


  1. Born J, Rasch B, Gais S: Sleep to remember. Neuroscientist. 2006, 410-424.Google Scholar
  2. Olbrich E, Achermann P: Analysis of oscillatory patterns in the human sleep EEG using a novel detection algorithm. J Sleep Res. 2005, 14: 337-346. 10.1111/j.1365-2869.2005.00475.x.PubMedView ArticleGoogle Scholar
  3. Olbrich E, Wennekers T: Dynamics of parameters of neurophysiological models from phenomenological EEG modelling. Neurocomputing. 2007, 70: 1848-1852. 10.1016/j.neucom.2006.10.108.View ArticleGoogle Scholar


© Olbrich and Wennekers; licensee BioMed Central Ltd. 2009

This article is published under license to BioMed Central Ltd.