J
jneutron
Senior Audioholic
You have got to be kidding me...if you don't send all four to me, I will hunt you down..Swerd said:Email me if you want any of these full articles in pdf form.
They need to learn how to write an abstract if they wanna sell papers..it would be nice to know what the way is they allude to.Banks, M. S. (2004). "Neuroscience: what you see and hear is what you get." Curr Biol 14(6): R236-8.
The brain receives signals from a variety of sources; for example, visual and auditory signals can both indicate the direction of a stimulus, but with differing precision. A recent study has shed light on the way that the brain combines these signals to achieve the best estimate possible.
Now, THAT's an abstract...I'm chompin at the bit.....it'll be interesting to see if their method of transposition is in any way similar to Nordmark's jitter method. Nordmark has 500 hz as the start of lateralization sensitivity, 1.2Khz as the end of unjittered sensitivity, and 12K plus with jitter included.Bernstein, L. R. (2001). "Auditory processing of interaural timing information: new insights." J Neurosci Res 66(6): 1035-46.
Differences in the time-of-arrival of sounds at the two ears, or interaural temporal disparities (ITDs), constitute one of the major binaural cues that underlie our ability to localize sounds in space. In addition, ITDs contribute to our ability to detect and to discriminate sounds, such as speech, in noisy environments. For low-frequency signals, ITDs are conveyed primarily by "cycle-by-cycle" disparities present in the fine-structure of the waveform. For high-frequency signals, ITDs are conveyed by disparities within the time-varying amplitude, or envelope, of the waveform. The results of laboratory studies conducted over the past few decades indicate that ITDs within the envelopes of high-frequency are less potent than those within the fine-structure of low-frequency stimuli. This is true for both measures of sensitivity to changes in ITD and for measures of the extent of the perceived lateral displacement of sounds containing ITDs. Colburn and Esquissaud (1976) hypothesized that it is differences in the specific aspects of the waveform that are coded neurally within each monaural (single ear) channel that account for the greater potency of ITDs at low frequencies rather than any differences in the more central binaural mechanisms that serve these different frequency regions. In this review, the results of new studies are reported that employed special high-frequency "transposed" stimuli that were designed to provide the high-frequency channels of the binaural processor with envelope-based information that mimics waveform-based information normally available only in low-frequency channels. The results demonstrate that these high-frequency transposed stimuli (1) yield sensitivity to ITDs that approaches, or is equivalent to, that obtained with "conventional" low-frequency stimuli and (2) yield large extents of laterality that are similar to those measured with conventional low-frequency stimuli. These findings suggest that by providing the high-frequency channels of the binaural processor with information that mimics that normally available only at low frequencies, the potency of ITDs in the two frequency regions can be made to be similar, if not identical. These outcomes provide strong support for Colburn and Esquissaud's (1976) hypothesis. The use of high-frequency transposed stimuli, in both behavioral and physiological investigations offers the promise of new and important insights into the nature of binaural processing.
They seem to be a bit confused with their conduction delay speak, as delay lines won't help lateralization, unless they are talking about the same thing digital filter guys do. Not a clear abstract...McAlpine, D. and B. Grothe (2003). "Sound localization and delay lines--do mammals fit the model?" Trends Neurosci 26(7): 347-50.
The current dominant model of binaural sound localization proposes that the lateral position of a sound source is determined by the position of maximal activation within an array of binaural coincidence-detector neurons that are tuned to different interaural time differences (ITDs). The tuning of a neuron for an ITD is determined by the difference in axonal conduction delay from each ear--the so-called "delay line" hypothesis. Although studies in birds appear to support this model, recent evidence from mammals suggests that the model does not provide accurate descriptions of how ITDs are encoded in the mammalian auditory brainstem or of how ITD-sensitive neurons contribute to mammalian sound localization.
Better abstract..Schnupp, J. (2001). "Of delays, coincidences and efficient coding for space in the auditory pathway." Trends Neurosci 24(12): 677-8.
To localize a sound source in space, the auditory system detects minute differences in the arrival time of a sound between the two ears. It has long been assumed that delay lines and coincidence detectors turn these time differences into a labelled line code for source position, but recent studies challenge this view.
From the abstracts, I certainly agree.After a quick read, I think the Bernstein article might be the most useful.
Their model is gonna hafta include the ability to detect simultaneous frequencies from one source as well..
Thank you very much, Swerd..I look forward to the reading.
Cheers, John