Evidence map›Paper›PMID 24848460›Full record

ArticleJournal of neurophysiology2014

On the localization of complex sounds: temporal encoding based on input-slope coincidence detection of envelopes.

Yan Gai, Vibhakar C Kotak, Dan H Sanes, John Rinzel

Open access · greenAbstract 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 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 29% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. The impact of peripheral mechanisms on the precedence effect.The Journal of the Acoustical Society of America · 2019
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
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

4 authors at 2 institutions in 1 country.

Yan GaiDepartment of Neuroscience, University of Wisconsin Madison, Madison, Wisconsin; Center for Neural Science, New York University, New York, New York;
Vibhakar C KotakCenter for Neural Science, New York University, New York, New York;
Dan H SanesCenter for Neural Science, New York University, New York, New York; Department of Biology, New York University, New York, New York; and.
John RinzelDepartment of Biology, New York University, New York, New York; and Courant Institute of Mathematical Science, New York University, New York, New York rinzeljm@gmail.com.
New York University · USCourant Institute of Mathematical Sciences · US

Funding

Rescue of cortical inhibitory synapses following developmental hearing lossR01DC011284 · NIDCD · NEW YORK UNIVERSITY · PI SANES, DAN HARVEY · 2011 to 2022
$5.4M
Biophysical Specializations Enrich Temporal Selectivity of MSO NeuronsR01DC008543 · NIDCD · NEW YORK UNIVERSITY · PI RINZEL, JOHN M · 2007 to 2011
$1.9M
NIDCD NIH HHS DC008543NIDCD NIH HHS DC011284NIDCD NIH HHS R01 DC008543NIDCD NIH HHS R01 DC011284
6 · The paper itself

Abstract

Behavioral and neural findings demonstrate that animals can locate low-frequency sounds along the azimuth by detecting microsecond interaural time differences (ITDs). Information about ITDs is also available in the amplitude modulations (i.e., envelope) of high-frequency sounds. Since medial superior olivary (MSO) neurons encode low-frequency ITDs, we asked whether they employ a similar mechanism to process envelope ITDs with high-frequency carriers, and the effectiveness of this mechanism compared with the process of low-frequency sound. We developed a novel hybrid in vitro dynamic-clamp approach, which enabled us to mimic synaptic input to brain-slice neurons in response to virtual sound and to create conditions that cannot be achieved naturally but are useful for testing our hypotheses. For each simulated ear, a virtual sound, computer generated, was used as input to a computational auditory-nerve model. Model spike times were converted into synaptic input for MSO neurons, and ITD tuning curves were derived for several virtual-sound conditions: low-frequency pure tones, high-frequency tones modulated with two types of envelope, and speech sequences. Computational models were used to verify the physiological findings and explain the biophysical mechanism underlying the observed ITD coding. Both recordings and simulations indicate that MSO neurons are sensitive to ITDs carried by spectrotemporally complex virtual sounds, including speech tokens. Our findings strongly suggest that MSO neurons can encode ITDs across a broad-frequency spectrum using an input-slope-based coincidence-detection mechanism. Our data also provide an explanation at the cellular level for human localization performance involving high-frequency sound described by previous investigators.

Indexed as

Evoked Potentials, AuditoryModels, NeurologicalSound LocalizationAnimalsCochlear NerveGerbillinaeHumansNeuronsSpeech PerceptionSuperior Olivary Complexauditory processingKv1.1phasic firingsound localization

Identifiers

PMID24848460
PMCPMC4122752
OpenAlexW2317889844

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.