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Accessing brain activity non-invasively using neuroimaging techniques has been possible for about two decades and has continued to thrive from the technical and methodological standpoints (K. J. Friston, 2009). With the ubiquitous availability of magnetic resonance imaging (MRI) scanners in major hospitals and research centers, functional-MRI (fMRI) has certainly become the modality-of-choice to approach the human brain in action. A well-documented and thoroughly-discussed limitation of fMRI however, sits in the very physiological origins of the signals accessible to the analysis. Indeed, fMRI is essentially sensitive to local fluctuations in blood oxygen levels and flow, which connexion to cerebral activity is the object of very active scientific investigations and sometimes, controversies (Logothetis & Pfeuffer, 2004, Logothetis & Wandell, 2004, Eijsden, Hyder, Rothman, & Shulman, 2009). A more fundamental limitation of fMRI and metabolic techniques such as Positron Emission Tomography (PET) is the lack of temporal resolution.
In essence, the physiological changes captured by these techniques fluctuate within a typical time scale of several hundreds of milliseconds at best, which makes them excellent at mapping the regions involved in task performance or resting-states (Fox & Raichle, 2007), but incapable of resolving the flow of rapid brain activity that unfolds with time. Metaphorically speaking, metabolic and hemodynamic techniques perform as very sensitive cameras that are able to capture low-intensity signals using long aperture durations, hence a sluggish temporal resolution. This basic limitation has become salient as new neuroscience questions emerge to investigate the brain as an ensemble of complex networks that form, reshape and flush information dynamically (Varela, Lachaux, Rodriguez, & Martinerie, 2001, Sergent & Dehaene, 2004, Werner, 2007).
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