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Licensed Unlicensed Requires Authentication Published by De Gruyter July 19, 2014

Short-term learning effect in different psychoacoustic measures

  • Leah Fostick EMAIL logo , Shira Wechsler and Elisheva Peretz

Abstract

Background: Learning effect has been studied in the literature, but the learning done in short-term training has not been studied. Also, to date, the learning effect of different psychoacoustic measures has not been compared. In the current study, we compared the perceptual learning effect caused by performing four different auditory temporal processing (ATP) tasks in a short-term training design including two training sessions.

Methods: A total of 74 young, normal-hearing participants each performed one of the following tasks: spectral temporal order judgment (TOJ), dichotic TOJ, gap detection, or duration discrimination. Each task was performed in two consecutive sessions.

Results: A learning effect was observed only for the spectral TOJ task. The change from the first to the second session was larger in spectral TOJ (81%) than in dichotic TOJ (2%), gap detection (7%), and duration discrimination (5%).

Conclusions: The difference in perceptual learning between spectral TOJ and other ATP tasks suggests that the performance of this task involves other cue(s) in addition to the temporal one.


Corresponding author: Leah Fostick, Department of Communication Disorders, Ariel University, Ariel, Israel, Phone: +972-3-9765776, Fax: +972-3-975-8908, E-mail:

Conflict of interest statement

Authors’ conflict of interest disclosure: The authors stated that there are no conflicts of interest regarding the publication of this article.

Research funding: None declared.

Employment or leadership: None declared.

Honorarium: None declared.

References

1. Fostick L, Babkoff H. Different response patterns between auditory spectral and spatial temporal order. Exp Psychol 2013;60:432–43.10.1027/1618-3169/a000216Search in Google Scholar

2. Fostick L, Babkoff H. Temporal and non-temporal processes in the elderly. J Basic Clin Physiol Pharmacol 2013;24:191–9.10.1515/jbcpp-2013-0049Search in Google Scholar

3. Boehnke SE, Phillips DP. The relation between auditory temporal interval processing and sequential stream segregation examined with stimulus laterality differences. Percept Psychophys 2005;67:1088–101.10.3758/BF03193634Search in Google Scholar

4. Heisterueber M, Klein E, Willmes K, Heim S, Domahs F. Processing word prosody – behavioral and neuroimaging evidence for heterogeneous performance in a language with variable stress. Front Psychol 2014;5:365.10.3389/fpsyg.2014.00365Search in Google Scholar

5. Lapid E, Ulrich R, Rammsayer T. On estimating the difference limen in duration discrimination tasks: a comparison of the 2AFC and the reminder task. Percept Psychophys 2008;70: 291–305.10.3758/PP.70.2.291Search in Google Scholar

6. Szymaszek A, Szelag E, Sliwowska M. Auditory perception of temporal order in humans: the effect of age, gender, listener practice and stimulus presentation mode. Neurosci Lett 2006;403:190–4.10.1016/j.neulet.2006.04.062Search in Google Scholar

7. Szymaszek A, Sereda M, Pöppel E, Szelag E. Individual differences in the perception of temporal order: the effect of age and cognition. Cogn Neuropsychol 2009;26:135–47.10.1080/02643290802504742Search in Google Scholar

8. von Steinbuchel N. Temporal ranges of central nervous processing: clinical evidence. Exp Brain Res 1998;123:220–33.10.1007/s002210050564Search in Google Scholar

9. von Steinbuchel N, Wittmann M, Strasburger H, Szelag E. Auditory temporal-order judgement is impaired in patients with cortical lesions in posterior regions of the left hemisphere. Neurosci Lett 1999;264:168–71.10.1016/S0304-3940(99)00204-9Search in Google Scholar

10. Fink M, Churan J, Wittmann M. Temporal processing and context dependency of phoneme discrimination in patients with aphasia. Brain Lang 2006;98:1–11.10.1016/j.bandl.2005.12.005Search in Google Scholar PubMed

11. Wittmann M, Burtscher A, Fries W, von Steinbüchel N. Effects of lesion size and location on temporal-order judgement in brain-injured patients. Neuroreport 2004;15:2401–5.10.1097/00001756-200410250-00020Search in Google Scholar

12. Ben-Artzi E, Fostick L, Babkoff H. Deficits in temporal-order judgments in dyslexia: evidence from diotic stimuli differing spectrally and from dichotic stimuli differing only by perceived location. Neuropsychologia 2005;43:714–23.10.1016/j.neuropsychologia.2004.08.004Search in Google Scholar

13. Fostick L, Bar-El S, Ram-Tsur R. Auditory temporal processing as a specific deficit among dyslexic readers. Psychol Res 2012;2:77–88.10.17265/2159-5542/2012.02.001Search in Google Scholar

14. Tallal P. Auditory temporal perception, phonics, and reading disabilities in children. Brain Lang 1980;9:182–98.10.1016/0093-934X(80)90139-XSearch in Google Scholar

15. Reed MA. Speech perception and the discrimination of brief auditory cues in reading disabled children. J Exp Child Psychol 1989;48:270–92.10.1016/0022-0965(89)90006-4Search in Google Scholar

16. Hämäläinen JA, Salminen HK, Leppänen PH. Basic auditory processing deficits in dyslexia: systematic review of the behavioral and event-related potential/field evidence. J Learn Disabil 2013;46:413–27.10.1177/0022219411436213Search in Google Scholar

17. Ben-Artzi E, Babkoff H, Fostick L. Auditory temporal processes in the elderly. Audiol Res 2011;1:e6.10.4081/audiores.2011.e6Search in Google Scholar

18. Fink M, Churan J, Wittmann M. Assessment of auditory temporal-order thresholds – a comparison of different measurement procedures and the influences of age and gender. Restor Neurol Neurosci 2005;23:281–96.Search in Google Scholar

19. Kumar AU, A V S. Temporal processing abilities across different age groups. J Am Acad Audiol 2011;22:5–12.10.3766/jaaa.22.1.2Search in Google Scholar

20. Kwakye LD, Foss-Feig JH, Cascio CJ, Stone WL, Wallace MT. Altered auditory and multisensory temporal processing in autism spectrum disorders. Front Integr Neurosci 2011;4:129.10.3389/fnint.2010.00129Search in Google Scholar

21. Breier JI, Gray LC, Fletcher JM, Foorman B, Klaas P. Perception of speech and nonspeech stimuli by children with and without reading disability and attention deficit hyperactivity disorder. J Exp Child Psychol 2002;82:226–50.10.1016/S0022-0965(02)00005-XSearch in Google Scholar

22. Kleiner M, Negbi M, Or R, Zuaretz C, Fostick L. Stimulants effect on behavioral and nonbehavioral auditory measures among ADHD students. Paper presented at the ASHA Convention, November 2011, San Diego, CA.Search in Google Scholar

23. Babkoff H, Zukerman G, Fostick L, Ben-Artzi E. Effect of the diurnal rhythm and 24 h of sleep deprivation on dichotic temporal order judgment. J Sleep Res 2005;14:7–15.10.1111/j.1365-2869.2004.00423.xSearch in Google Scholar

24. Fostick L, Babkoff H, Zukerman G. Effect of 24 h of sleep deprivation on auditory and linguistic perception: a comparison with dyslexic readers and aging adults. J Speech Lang Hear Res 2014;57:1078–88.10.1044/1092-4388(2013/13-0031)Search in Google Scholar

25. Hauptmann B, Karni A. From primed to learn: the saturation of repetition priming and the induction of long-term memory. Brain Res Cogn Brain Res 2002;13:313–22.10.1016/S0926-6410(01)00124-0Search in Google Scholar

26. Demany L. Perceptual learning in frequency discrimination. J Acoust Soc Am 1985;78:1118–20.10.1121/1.393034Search in Google Scholar PubMed

27. Goldstone RL. Perceptual learning. Annu Rev Psychol 1998;49:585–612. Percept Perform 35:188–94.10.1146/annurev.psych.49.1.585Search in Google Scholar PubMed

28. Goedert KM, Miller J. Spacing practice sessions across days earlier rather than later in training improves performance of a visuomotor skill. Exp Brain Res 2008;189:189–97.10.1007/s00221-008-1414-9Search in Google Scholar PubMed

29. Molloy K, Moore DR, Sohoglu E, Amitay S. Less is more: latent learning is maximized by shorter training sessions in auditory perceptual learning. Plos One 2012;30:1–13.10.1371/journal.pone.0036929Search in Google Scholar PubMed PubMed Central

30. Ari-Even Roth D, Appelbaum M, Milo C, Kishon-Rabin L. Generalization to untrained conditions following training with identical stimuli. J Basic Clin Physiol Pharmacol 2008;19:223–36.Search in Google Scholar

31. Alais D, Cass J. Multisensory perceptual learning of temporal order: audiovisual learning transfers to vision but not audition. Plos One 2010;5.10.1371/journal.pone.0011283Search in Google Scholar PubMed PubMed Central

32. Murphy CF, Schochat E. Effect of nonlinguistic auditory training on phonological and reading skills. Folia Phoniatr Logop 2011;63:147–53.10.1159/000316327Search in Google Scholar PubMed

33. Wright BA, Sabin AT. Perceptual learning: how much daily training is enough? Exp Brain Res 2007;180:727–36.10.1007/s00221-007-0898-zSearch in Google Scholar PubMed

34. Schneider BA, Pichora-Fuller MK, Kowalchuk D, Lamb M. Gap detection and the precedence effect in young and old adults. J Acoust Soc Am 1994;95:980–91.10.1121/1.408403Search in Google Scholar

35. Bratzke D, Seifried T, Ulrich R. Perceptual learning in temporal discrimination: asymmetric cross-modal transfer from audition to vision. Exp Brain Res 2012;221:205–10.10.1007/s00221-012-3162-0Search in Google Scholar

36. Bratzke D, Schroter H, Ulrich R. The role of consolidation for perceptual learning in temporal discrimination within and across modalities. Acta Psychol 2014;147:75–9.10.1016/j.actpsy.2013.06.018Search in Google Scholar

37. Wright B, Wilson R, Sabin S. Generalization lags behind learning on an auditory perceptual task. J Neurosci 2010;30:11635–9.10.1523/JNEUROSCI.1441-10.2010Search in Google Scholar

38. Kishon-Rabin L, Avivi-Reich M, Ari-Even Roth D. Improved gap detection thresholds following auditory training: evidence of auditory plasticity in older adults. Am J Audiol 2013;22:343–6.10.1044/1059-0889(2013/12-0084)Search in Google Scholar

39. Roth DA, Appelbaum M, Milo C, Kishon-Rabin L. Generalization to untrained conditions following training with identical stimuli. J Basic Clin Physiol Pharmacol 2008;19:223–36.10.1515/JBCPP.2008.19.3-4.223Search in Google Scholar PubMed

40. Roth DA, Refael-Taub R, Sharvit R, Kishon-Rabin L. Can learning a frequency discrimination task occur without discrimination? J Basic Clin Physiol Pharmacol 2006;17:159–71.10.1515/JBCPP.2006.17.3.159Search in Google Scholar

41. Kishon-Rabin L, Amir O, Vexler Y, Zaltz Y. Pitch discrimination: are professional musicians better than non-musicians? J Basic Clin Physiol Pharmacol 2001;12(2 suppl):125–43.10.1515/JBCPP.2001.12.2.125Search in Google Scholar

42. Agus TR, Pressnitzer D. The detection of repetitions in noise before and after perceptual learning. J Acoust Soc Am 2013;134:464–73.10.1121/1.4807641Search in Google Scholar PubMed

43. Huyck JJ, Wright BA. Learning, worsening, and generalization in response to auditory perceptual training during adolescence. J Acoust Soc Am 2013;134:1172–82.10.1121/1.4812258Search in Google Scholar PubMed PubMed Central

44. Cohen Y, Daikhin L, Ahissar M. Perceptual learning is specific to the trained structure of information. J Cogn Neurosci 2013;25:2047–60.10.1162/jocn_a_00453Search in Google Scholar PubMed

45. de Souza AC, Yehia HC, Sato MA, Callan D. Brain activity underlying auditory perceptual learning during short period training: simultaneous fMRI and EEG recording. BMC Neurosci 2013;14:8.10.1186/1471-2202-14-8Search in Google Scholar PubMed PubMed Central

46. Warren RM, Ackroff JM. Two types of auditory sequence perception. Percept Psychophys 1976;20:387–94.10.3758/BF03199420Search in Google Scholar

Received: 2014-3-26
Accepted: 2014-6-14
Published Online: 2014-7-19
Published in Print: 2014-9-1

©2014 by De Gruyter

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