Skip to main content
Log in

Something (important) is out there! Effects of prime arousal and location on evaluative priming

  • Original Paper
  • Published:
Motivation and Emotion Aims and scope Submit manuscript

Abstract

The ability of an organism to rapidly process parafoveal information to identify motivationally significant stimuli is important for survival. The evaluative priming paradigm is useful for examining whether evaluation of hostile/hospitable stimuli in the parafovea has occurred. Three evaluative priming experiments that varied the valence and arousal of prime stimuli were conducted. In the first experiment, primes were presented foveally and prime arousal did not moderate the standard evaluative priming effect (i.e., faster responses when prime and target valence matched). In the next two experiments, primes were presented parafoveally and prime arousal moderated evaluative priming such that priming was greater for high than low arousing primes. These findings are aligned with dual competition models positing that sensory and response systems compete for limited resources during emotional processing. Greater stimulus arousal enhances this dual competition during parafoveal processing, enabling the organisms to disengage and attend to the periphery.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

Notes

  1. By “parafoveal processing”, we mean the processes involved in detecting stimuli that are outside of central focus. These processes may very well overlap with many of the “covert attentional” processes that have been extensively reviewed elsewhere (Carrasco 2011). However, because we are not directly manipulating nor measuring covert attention, we prefer terminology more in line with the actual manipulation of the present work.

  2. The rationale for this criterion is that most participants' accuracy that is 2.5 SDs below the grand mean in this paradigm is either slightly above chance (e.g., 54 %) or grossly deviant from the grant mean (e.g. 23 %). These participants' responses were deemed aberrant and therefore these participants were not included in the main analysis (as in Herring et al. 2011). Including this participant in the analysis yielded the same findings reported below. The evaluative congruity effect was F(1, 51) = 17.23, p < .001, ηη 2p  = .25, and was evident for both high, t(51) = 3.43, p = .001, d = 0.47, and low arousing prime conditions, t(51) = 3.43, p = .001, d = 0.51.

  3. With primes and targets varying in arousal level (high vs. low) we performed an exploratory analysis when primes and targets were congruent (e.g., high arousing prime-high arousing target) or incongruent in arousal (e.g., low arousing prime-high arousing target). Only was there evidence of arousal congruity in Experiment 2, F(1, 53) = 4.35, p = .04, ηη 2p  = .08. When target arousal was low, RTs were slower to high (M = 746 ms, SD = 86 ms) than low (M = 735, SD = 87 ms) arousing primes, t(53) = 3.62, p < .001, d = 0.49. There were no difference in RTs for high arousing targets preceded by high (M = 743, SD = 88) and low (M = 740 ms, SD = 87 ms) arousing primes, t(53) = 0.76, p = .44, d = 0.10. Thus, there was some evidence of arousal priming but only for low but not high arousing targets.

  4. We suggested in our meta-analytic review of the evaluative priming literature that prime by target valence interaction be reported instead of collapsing these variables into a congruity main effect as reported here (Herring et al. 2013). This recommendation was made to develop more sophisticated theoretical models of evaluative priming taking prime and target valence into consideration (see Unkelbach et al. 2008). For didactic reasons, we report the congruency analyses in the body of the text and review the findings from the analysis involving prime by target valence in footnotes. In Experiment 1, there was a main effect of target valence, F(1, 50) = 21.30, p < .001, ηη 2p  = 0.30, such that unpleasant targets (M = 691 ms, SD = 87 ms) were responded to more quickly than pleasant targets (M = 724 ms, SD = 100 ms). .

  5. The interaction test between evaluative congruity and prime arousal was F(1, 50) = .66, p = .42, ηη 2p  = 0.01.

  6. Including these three participants in the analysis (n = 1 for Experiment 2 and n = 2 from Experiment 3) yielded the same findings reported below. The evaluative congruity effects were F(1, 54) = 6.51, p = .01, η 2p  = 0.11, and F(1, 58) = 6.60, p = .01, η 2p  = 0.10. Evaluative priming remained evident for high, t(54) = 3.62, p < .001, d = 0.48, t(58) = 3.02, p = .003, d = 0.39, but not low arousing prime conditions, t(54) = 0.75, p = .45, d = 0.10 and t(58) = 0.68, p = .49, d = 0.09, respectively, for experiments 2 and 3.

  7. Note that this stimulus size differs from previous evaluative priming studies using parafoveal primes (Calvo and Avero 2008; Calvo and Nummenmaa 2007). Nonetheless, our stimuli were still presented parafoveally given greater screen resolution and size.

  8. There was also a significant prime arousal by prime valence interaction, F(1, 53) = 4.75, p = .03, ηη 2p  = 0.08. Targets preceded by low arousing, pleasant primes were responded to more quickly (M = 734 ms, SD = 85 ms) than those preceded by low arousing, unpleasant primes (M = 741 ms, SD = 89 ms), t(53) = 2.08, p = .04, d = 0.28. However, there was no difference between targets preceded by high arousing, pleasant primes (M = 746, SD = 88 ms) and high arousing, unpleasant primes (M = 742 ms, SD = 86 ms), t(53) = 1.29, p = .19, d = 0.17.

  9. The interaction tests between evaluative congruity and prime arousal were F(1, 53) = 5.52, p = .022, ηη 2p  = 0.09, and F(1, 56) = 1.96, p = .16, ηη 2p  = 0.03, respectively, for Experiments 2 and 3.

  10. Replicating Experiment 2, there was a prime arousal by prime valence interaction, F(1, 56) = 8.50, p = .005, ηη 2p  = 0.13. Targets preceded by low arousing, pleasant primes were responded to more quickly (M = 711 ms, SD = 103 ms) than low arousing, unpleasant primes (M = 719 ms, SD = 101 ms), t(56) = 2.95, p = .004, d = 0.39. However, there was no difference between targets preceded by high arousing, pleasant primes (M = 721, SD = 99 ms) than high arousing, unpleasant primes (M = 719 ms, SD = 100 ms), t(56) = .76, p = .44, d = 0.10.

References

  • Bartholow, B. D., Riordan, M. A., Saults, J. S., & Lust, S. A. (2009). Psychophysiological evidence of response conflict and strategic control of responses in affective priming. Journal of Experimental Social Psychology, 45, 655–666. doi:10.1016/j.jesp.2009.02.015.

    Article  Google Scholar 

  • Bradley, M. M., & Lang, P. J. (1994). Measuring emotion: The self-assessment manikin and the semantic differential. Journal of Behavior Therapy and Experimental Psychiatry, 25, 49–59.

    Article  PubMed  Google Scholar 

  • Bradley, M. M., & Lang, P. J. (2007). Emotion and motivation. In J. T. Cacioppo, L. G. Tassinary, & G. G. Berntson (Eds.), Handbook of psychophysiology (Vol. 3rd, pp. 581–607). New York, NY: Cambridge University Press. http://search.ebscohost.com/login.aspx?direct=true&db=psyh&AN=2007-08652-025&site=ehost-live&scope=site.

  • Calvo, M. G., & Avero, P. (2008). Affective priming of emotional pictures in parafoveal vision: Left visual field advantage. Cognitive, Affective & Behavioral Neuroscience, 8, 41–53. doi:10.3758/CABN.8.1.41.

    Article  Google Scholar 

  • Calvo, M. G., & Nummenmaa, L. (2007). Processing of unattended emotional visual scenes. Journal of Experimental Psychology: General, 136, 347–369. doi:10.1037/0096-3445.136.3.347.

    Article  Google Scholar 

  • Calvo, M. G., Nummenmaa, L., & Avero, P. (2010). Recognition advantage of happy faces in extrafoveal vision: Featural and affective processing. Visual Cognition, 18, 1274–1297. doi:10.1080/13506285.2010.481867.

    Article  Google Scholar 

  • Carrasco, M. (2011). Visual attention: The past 25 years. Vision Research, 51(13), 1484–1525. doi:10.1016/j.visres.2011.04.012.

    Article  PubMed Central  PubMed  Google Scholar 

  • Cohen, N., & Henik, A. (2012). Do irrelevant emotional stimuli impair or improve executive control? Frontiers in Integrative Neuroscience, 6. doi:10.3389/fnint.2012.00033

  • Cremers, H. R., Demenescu, L. R., Aleman, A., Renken, R., van Tol, M.-J., van der Wee, N. J. A., & Roelofs, K. (2010). Neuroticism modulates amygdala—prefrontal connectivity in response to negative emotional facial expressions. NeuroImage, 49(1), 963–970. doi:10.1016/j.neuroimage.2009.08.023.

    Article  PubMed  Google Scholar 

  • Fazio, R. H., Sanbonmatsu, D. M., Powell, M. C., & Kardes, F. R. (1986). On the automatic activation of attitudes. Journal of Personality and Social Psychology, 50, 229–238. doi:10.1037/0022-3514.50.2.229.

    Article  PubMed  Google Scholar 

  • Giner-Sorolla, R., García, M. T., & Bargh, J. A. (1999). The automatic evaluation of pictures. Social Cognition, 17, 76–96. doi:10.1521/soco.1999.17.1.76.

    Article  Google Scholar 

  • Herring, D. R., Taylor, J. H., White, K. R., & Crites, S. L. (2011). Electrophysiological responses to evaluative priming: The LPP is sensitive to incongruity. Emotion, 11, 794–806. doi:10.1037/a0022804.

    Article  PubMed  Google Scholar 

  • Herring, D. R., White, K. R., Jabeen, L. N., Hinojos, M., Terrazas, G., Reyes, S. M., & Crites, S. L. (2013). On the automatic activation of attitudes: A quarter century of evaluative priming research. Psychological Bulletin, 139(5), 1062–1089. doi:10.1037/a0031309.

    Article  PubMed  Google Scholar 

  • Hinojosa, J. A., Carretié, L., Méndez-Bértolo, C., Míguez, A., & Pozo, M. A. (2009). Arousal contributions to affective priming: Electrophysiological correlates. Emotion, 9, 164–171. doi:10.1037/a0014680.

    Article  PubMed  Google Scholar 

  • Keil, A., Moratti, S., Sabatinelli, D., Bradley, M. M., & Lang, P. J. (2005). Additive effects of emotional content and spatial selective attention on electrocortical facilitation. Cerebral Cortex, 15(8), 1187–1197. doi:10.1093/cercor/bhi001.

    Article  PubMed  Google Scholar 

  • Keil, A., Sabatinelli, D., Ding, M., Lang, P. J., Ihssen, N., & Heim, S. (2009). Re-entrant projections modulate visual cortex in affective perception: Evidence from Granger causality analysis. Human Brain Mapping, 30(2), 532–540. doi:10.1002/hbm.20521.

    Article  PubMed Central  PubMed  Google Scholar 

  • Kiefer, M. (2007). Top-down modulation of unconscious “automatic” processes: A gating framework. Advances in Cognitive Psychology, 3, 289–306. doi:10.2478/v10053-008-0031-2.

    Article  PubMed Central  Google Scholar 

  • Klauer, K. C., & Musch, J. (2003). Affective priming: Findings and theories. In J. Musch & K. C. Klauer (Eds.), The psychology of evaluation: Affective processes in cognition and emotion (pp. 7–49). Mahwah, NJ: Lawrence Erlbaum Associates Publishers.

    Google Scholar 

  • Klauer, K. C., Teige-Mocigemba, S., & Spruyt, A. (2009). Contrast effects in spontaneous evaluations: A psychophysical account. Journal of Personality and Social Psychology, 96, 265–287. doi:10.1037/a0013248.

    Article  PubMed  Google Scholar 

  • Lang, P. J., & Bradley, M. M. (2007). The international affective picture system (IAPS) in the study of emotion and attention. In J. A. Coan & J. J. B. Allen (Eds.), Handbook of Emotion Elicitation and Assessment (pp. 29–46). New York: Oxford University Press.

    Google Scholar 

  • Lang, P. J., Bradley, M. M., & Cuthbert, B. N. (2008). International affective picture system (IAPS): Affective ratings of pictures and instruction manual. Technical Report A-8. University of Florida, Gainesville, FL.

  • Lang, P. J., Bradley, M. M., Fitzsimmons, J. R., Cuthbert, B. N., Scott, J. D., Moulder, B., & Nangia, V. (1998). Emotional arousal and activation of the visual cortex: An fMRI analysis. Psychophysiology, 35(2), 199–210.

    Article  PubMed  Google Scholar 

  • Mehrabian, A., & Russell, J. A. (1974). An approach to environmental psychology (Vol. xii). Cambridge, MA, US: The MIT Press.

    Google Scholar 

  • Melcher, T., Born, C., & Gruber, O. (2011). How negative affect influences neural control processes underlying the resolution of cognitive interference: An event-related fMRI study. Neuroscience Research, 70(4), 415–427. doi:10.1016/j.neures.2011.05.007.

    Article  PubMed  Google Scholar 

  • Monosov, I. E., Trageser, J. C., & Thompson, K. G. (2008). Measurements of simultaneously recorded spiking activity and local field potentials suggest that spatial selection emerges in the frontal eye field. Neuron, 57(4), 614–625. doi:10.1016/j.neuron.2007.12.030.

    Article  PubMed Central  PubMed  Google Scholar 

  • Nummenmaa, L., Hyona, J., & Calvo, M. G. (2008). Do emotional scenes catch the eyes? In K. Rayner, X. B. Shen, & G. Yan (Eds.), Cognitive and cultural influences on eye movements (pp. 175–195). Hove: Psychology Press.

    Google Scholar 

  • Oldfield, R. C. (1971). The assessment and analysis of handedness: The Edinburgh inventory. Neuropsychologia, 9, 97–113. doi:10.1016/0028-3932(71)90067-4.

    Article  PubMed  Google Scholar 

  • Osgood, C. E., Suci, C. J., & Tannenbaum, P. (1957). The measurement of meaning. Urbana, IL: University of Illinois Press.

    Google Scholar 

  • Pessoa, L. (2009). How do emotion and motivation direct executive control? Trends in Cognitive Sciences, 13(4), 160–166. doi:10.1016/j.tics.2009.01.006.

    Article  PubMed Central  PubMed  Google Scholar 

  • Pourtois, G., Thut, G., Grave de Peralta, R., Michel, C., & Vuilleumier, P. (2005). Two electrophysiological stages of spatial orienting towards fearful faces: early temporo-parietal activation preceding gain control in extrastriate visual cortex. NeuroImage, 26(1), 149–163. doi:10.1016/j.neuroimage.2005.01.015.

    Article  PubMed  Google Scholar 

  • Rayner, K. (1998). Eye movements in reading and information processing: 20 years of research. Psychological Bulletin, 124, 372–422. doi:10.1037/0033-2909.124.3.372.

    Article  PubMed  Google Scholar 

  • Schneider, W., Eschman, A., & Zuccolotto, A. (2002). E-Prime user’s guide. Pittsburgh, PA: Psychology Software Tools Inc.

    Google Scholar 

  • Spruyt, A., Gast, A., & Moors, A. (2011). The sequential priming paradigm. In K. C. Klauer, A. Voss, & C. Stahl (Eds.), Cognitive methods in social psychology (pp. 49–77). New York, NY: Guilford Press.

    Google Scholar 

  • Spruyt, A., Houwer, J. D., & Hermans, D. (2009). Modulation of automatic semantic priming by feature-specific attention allocation. Journal of Memory and Language, 61, 37–54. doi:10.1016/j.jml.2009.03.004.

    Article  Google Scholar 

  • Thompson, K. G., Biscoe, K. L., & Sato, T. R. (2005). Neuronal basis of covert spatial attention in the frontal eye field. The Journal of Neuroscience, 25(41), 9479–9487. doi:10.1523/JNEUROSCI.0741-05.2005.

    Article  PubMed Central  PubMed  Google Scholar 

  • Ulrich, M., Adams, S. C., & Kiefer, M. (2014). Flexible establishment of functional brain networks supports attentional modulation of unconscious cognition. Human Brain Mapping. doi:10.1002/hbm.22566

  • Unkelbach, C., Fiedler, K., Bayer, M., Stegmüller, M., & Danner, D. (2008). Why positive information is processed faster: The density hypothesis. Journal of Personality and Social Psychology, 95, 36. doi:10.1037/0022-3514.95.1.36.

    Article  PubMed  Google Scholar 

  • Wittenbrink, B. (2007). Measuring attitudes through priming. In B. Wittenbrink & N. Schwarz (Eds.), Implicit measures of attitudes (pp. 17–58). New York, NY: Guilford Press.

    Google Scholar 

  • Zhang, Q., Kong, L., & Jiang, Y. (2012). The interaction of arousal and valence in affective priming: Behavioral and electrophysiological evidence. Brain Research, 1474, 60–72. doi:10.1016/j.brainres.2012.07.023.

    Article  PubMed Central  PubMed  Google Scholar 

Download references

Acknowledgments

We thank Larry Cohn, Wendy Francis, and Joe Tomaka for comments on earlier drafts.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to David R. Herring.

Additional information

Portions of this research were performed under an appointment awarded to the first author from the U.S. Department of Homeland Security (DHS) Scholarship Program, administered by the Oak Ridge Institute for Science and Education (ORISE) through an interagency agreement between the U.S. Department of Energy (DOE) and DHS. ORISE is managed by Oak Ridge Associated Universities (ORAU) under DOE contract number DE-AC05-06OR23100. All opinions expressed in this paper are the authors’ and do not necessarily reflect the policies and views of DHS, DOE, or ORAU/ORISE.

Appendix

Appendix

See Table 2.

Table 2 Pictures used in the current study from the IAPS

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Herring, D.R., White, K.R., Jabeen, L.N. et al. Something (important) is out there! Effects of prime arousal and location on evaluative priming. Motiv Emot 39, 742–752 (2015). https://doi.org/10.1007/s11031-015-9492-z

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11031-015-9492-z

Keywords

Navigation