Path: utzoo!utgpu!news-server.csri.toronto.edu!rpi!zaphod.mps.ohio-state.edu!mips!spool.mu.edu!agate!dino!brp From: brp@dino.berkeley.edu (Bruce Raoul Parnas) Newsgroups: bionet.neuroscience Subject: Re: Auditory Impulse Travel and Distance Message-ID: <1991Jun18.190748.14855@agate.berkeley.edu> Date: 18 Jun 91 19:07:48 GMT References: <9106171949.AA20716@genbank.bio.net> <1991Jun18.033141.11511@agate.berkeley.edu> Sender: usenet@agate.berkeley.edu (USENET Administrator) Distribution: bionet Organization: /etc/organization Lines: 26 In article slehar@park.bu.edu (Steve Lehar) writes: > >The reason why the brain uses neural spiking, and encodes signal >magnitude as spiking frequency is exactly to avoid the degredation >with distance that is experienced by the alternative method of neural >signaling, i.e. the density of ions of a particular charge. > i think the question here is not one of active vs. electrotonic spread of electrical activity through nerves, but of information transfer. signals which are weak, i.e. produce only a few spikes, could lose their identity in background firing rates of subsequent neurons. thus, spikes still propagate rather than dissipating, but the signal is lost. it turns out that in the auditory system this is probably not the case. the preponderance of the noise is at the front end, and signals are actually refined by ensemble processing as they travel along. thus, any signal that is lucky enough to make it past the cochlea and get transduced, i.e. pulled out from the noise, will very likely make it to the auditory cortex. >(O)((O))((( slehar@park.bu.edu )))((O))(O) >(O)((O))((( Steve Lehar Boston University Boston MA )))((O))(O) bruce (brp@bandit.berkeley.edu)