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When at rest: “Event-free” active inference may give rise to implicit self-models of coping potential

Published online by Cambridge University Press:  02 September 2015

Ryan J. Murray
Affiliation:
Laboratory for the Study of Emotion Elicitation and Expression, Department of Psychology, University of Geneva, 1205 Geneva, [email protected]://cms.unige.ch/fapse/EmotionLab/Members/ryan-murray/http://cms.unige.ch/fapse/EmotionLab/Members/david-sander/ Swiss Center for Affective Sciences, University of Geneva, 1211 Geneva, Switzerland
Philip Gerrans
Affiliation:
Swiss Center for Affective Sciences, University of Geneva, 1211 Geneva, Switzerland Department of Philosophy, University of Adelaide, Adelaide SA 5005, [email protected]://adelaide.academia.edu/PhilipGerrans
Tobias Brosch
Affiliation:
Swiss Center for Affective Sciences, University of Geneva, 1211 Geneva, Switzerland Consumer Decision and Sustainable Behavior Lab, Department of Psychology, University of Geneva, 1205 Geneva, [email protected]@unige.chhttps://www.unige.ch/fapse/decisionlab/people/tobias-brosch/
David Sander
Affiliation:
Laboratory for the Study of Emotion Elicitation and Expression, Department of Psychology, University of Geneva, 1205 Geneva, [email protected]://cms.unige.ch/fapse/EmotionLab/Members/ryan-murray/http://cms.unige.ch/fapse/EmotionLab/Members/david-sander/ Swiss Center for Affective Sciences, University of Geneva, 1211 Geneva, Switzerland

Abstract

Kalisch and colleagues highlight coping potential (CP) as a principle resilience mechanism during event engagement. We complement this discussion by exploring generative implicit CP self-models, arguably emerging during “resting-state,” subsequent and prior to events. Resting-state affords a propitious environment for Bayesian learning, wherein appraisals/reappraisals may update active inferential CP self-models, which then mediate appraisal style organization and resilience factor valuation.

Type
Open Peer Commentary
Copyright
Copyright © Cambridge University Press 2015 

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References

Back, M. D., Schmukle, S. C. & Egloff, B. (2009) Predicting actual behavior from the explicit and implicit self-concept of personality. Journal of Personality and Social Psychology 97(3):533–48. doi: 10.1037/a0016229.Google Scholar
Bengtsson, S. L. & Penny, W. D. (2013) Self-associations influence task-performance through Bayesian inference. Frontiers in Human Neuroscience 7:490. doi: 10.3389/fnhum.2013.00490.Google Scholar
Brosch, T. & Sander, D. (2013) The appraising brain: Towards a neuro-cognitive model of appraisal processes in emotion. Emotion Review 5(2):163–68. doi: 10.1177/1754073912468298.Google Scholar
D'Argembeau, A., Collette, F., Van der Linden, M., Laureys, S., Del Fiore, G., Degueldre, C., Luxen, A. & Salmon, E. (2005) Self-referential reflective activity and its relationship with rest: A PET study. NeuroImage 25(2):616–24. doi: 10.1016/j.neuroimage.2004.11.048.CrossRefGoogle Scholar
Ellsworth, P. C. & Scherer, K. R. (2003) Appraisal processes in emotion. In: Handbook of affective sciences, ed. Davidson, R. J., Scherer, K. R. & Goldsmith, H., pp. 572–95. Oxford University Press.Google Scholar
Friston, K. (2012) The history of the future of the Bayesian brain. NeuroImage 62(2):1230–33. doi: 10.1016/j.neuroimage.2011.10.004.CrossRefGoogle ScholarPubMed
Friston, K., Schwartenbeck, P., Fitzgerald, T., Moutoussis, M., Behrens, T. & Dolan, R. J. (2013) The anatomy of choice: Active inference and agency. Frontiers in Human Neuroscience 7:598. doi: 10.3389/fnhum.2013.00598.CrossRefGoogle ScholarPubMed
Gerrans, P. & Sander, D. (2014) Feeling the future: Prospects for a theory of implicit prospection. Biology and Philosophy 29(5):699710. doi: DOI 10.1007/s10539-013-9408-9.CrossRefGoogle Scholar
Helmholtz, H. V. & Southall, J. P. C. (1962) Helmholtz's treatise on physiological optics. Dover.Google Scholar
Moutoussis, M., Fearon, P., El-Deredy, W., Dolan, R. J. & Friston, K. J. (2014) Bayesian inferences about the self (and others): A review. Consciousness and Cognition 25:6776. doi: 10.1016/j.concog.2014.01.009.Google Scholar
Murray, R. J., Gerrans, P., Brosch, T. & Sander, D. (in preparation) From vulnerability to resilience: delineating the neural traits of social anxiety disorder.Google Scholar
Murray, R. J., Schaer, M. & Debbane, M. (2012) Degrees of separation: A quantitative neuroimaging meta-analysis investigating self-specificity and shared neural activation between self- and other-reflection. Neuroscience and Biobehavioral Reviews 36(3):1043–59. doi: 10.1016/j.neubiorev.2011.12.013.CrossRefGoogle ScholarPubMed
Ostby, Y., Walhovd, K. B., Tamnes, C. K., Grydeland, H., Westlye, L. T. & Fjell, A. M. (2012) Mental time travel and default-mode network functional connectivity in the developing brain. Proceedings of the National Academy of Sciences of the United States of America 109(42):16800–804. doi: 10.1073/pnas.1210627109.CrossRefGoogle ScholarPubMed
Qin, P. & Northoff, G. (2011) How is our self related to midline regions and the default-mode network? NeuroImage 57(3):1221–33. doi: S1053-8119(11)00516-7 [pii] 10.1016/j.neuroimage.2011.05.028.Google Scholar
Rameson, L. T., Satpute, A. B. & Lieberman, M. D. (2010) The neural correlates of implicit and explicit self-relevant processing. NeuroImage 50(2):701708. doi: S1053-8119(09)01387-1 [pii] 10.1016/j.neuroimage.2009.12.098.Google Scholar
Ruff, C. C. & Fehr, E. (2014) The neurobiology of rewards and values in social decision making. Nature Reviews Neuroscience 15(8):549–62. doi: 10.1038/nrn3776.Google Scholar
Schneider, F., Bermpohl, F., Heinzel, A., Rotte, M., Walter, M., Tempelmann, C., Wiebking, C., Dobrowolny, H., Heinze, H. J. & Northoff, G. (2008) The resting brain and our self: Self-relatedness modulates resting state neural activity in cortical midline structures. Neuroscience 157(1):120–31. doi: 10.1016/j.neuroscience.2008.08.014.CrossRefGoogle ScholarPubMed
Spreng, R. N. & Grady, C. L. (2010) Patterns of brain activity supporting autobiographical memory, prospection, and theory of mind, and their relationship to the default mode network. Journal of Cognitive Neuroscience 22(6):1112–23. doi: 10.1162/jocn.2009.21282.CrossRefGoogle ScholarPubMed