Evidence map›Paper›PMID 24554782›Full record

ArticleJournal of neurophysiology2014

Emphasis of spatial cues in the temporal fine structure during the rising segments of amplitude-modulated sounds II: single-neuron recordings.

Mathias Dietz, Torsten Marquardt, Annette Stange, Michael Pecka, Benedikt Grothe, David McAlpine

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.1field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Review
  3. Adaptation in auditory processing.Physiological reviews · 2023
    Review
  4. Temporal integration of monaural and dichotic frequency modulation.The Journal of the Acoustical Society of America · 2021
    Article
  5. Article
  6. Article
  7. The impact of peripheral mechanisms on the precedence effect.The Journal of the Acoustical Society of America · 2019
    Article
  8. Article
  9. Can monaural temporal masking explain the ongoing precedence effect?The Journal of the Acoustical Society of America · 2018
    Article
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  11. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Mathias DietzUniversity College London Ear Institute, London, United Kingdom; and mathias.dietz@uni-oldenburg.de.
Torsten MarquardtUniversity College London Ear Institute, London, United Kingdom; and.
Annette StangeDivision of Neurobiology, Department Biology II, Ludwig-Maximilians University, Munich, Germany.
Michael PeckaDivision of Neurobiology, Department Biology II, Ludwig-Maximilians University, Munich, Germany.
Benedikt GrotheDivision of Neurobiology, Department Biology II, Ludwig-Maximilians University, Munich, Germany.
David McAlpineUniversity College London Ear Institute, London, United Kingdom; and.
Ludwig-Maximilians-Universität München · DEUniversity College London · GB

Funding

Medical Research Council G1002267
6 · The paper itself

Abstract

Recently, with the use of an amplitude-modulated binaural beat (AMBB), in which sound amplitude and interaural-phase difference (IPD) were modulated with a fixed mutual relationship (Dietz et al. 2013b), we demonstrated that the human auditory system uses interaural timing differences in the temporal fine structure of modulated sounds only during the rising portion of each modulation cycle. However, the degree to which peripheral or central mechanisms contribute to the observed strong dominance of the rising slope remains to be determined. Here, by recording responses of single neurons in the medial superior olive (MSO) of anesthetized gerbils and in the inferior colliculus (IC) of anesthetized guinea pigs to AMBBs, we report a correlation between the position within the amplitude-modulation (AM) cycle generating the maximum response rate and the position at which the instantaneous IPD dominates the total neural response. The IPD during the rising segment dominates the total response in 78% of MSO neurons and 69% of IC neurons, with responses of the remaining neurons predominantly coding the IPD around the modulation maximum. The observed diversity of dominance regions within the AM cycle, especially in the IC, and its comparison with the human behavioral data suggest that only the subpopulation of neurons with rising slope dominance codes the sound-source location in complex listening conditions. A comparison of two models to account for the data suggests that emphasis on IPDs during the rising slope of the AM cycle depends on adaptation processes occurring before binaural interaction.

Indexed as

Acoustic StimulationAction PotentialsAlgorithmsAnimalsAuditory PerceptionCuesGerbillinaeGuinea PigsInferior ColliculiMicroelectrodesModels, NeurologicalNeuronsOlivary NucleusSound LocalizationSpace Perceptionbinaural processingextracellular recordingsinferior colliculusmedial superior olive

Identifiers

PMID24554782
PMCPMC4044336
OpenAlexW2009931292

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.