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Interaural timing difference circuits in the auditory brainstem of the emu ( Dromaius novaehollandiae )
Author(s) -
MacLeod Katrina M.,
Soares Daphne,
Carr Catherine E.
Publication year - 2006
Publication title -
journal of comparative neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.855
H-Index - 209
eISSN - 1096-9861
pISSN - 0021-9967
DOI - 10.1002/cne.20862
Subject(s) - biology , tonotopy , brainstem , interaural time difference , superior olivary complex , neuroscience , excitatory postsynaptic potential , nucleus , parvalbumin , anatomy , inhibitory postsynaptic potential , microstimulation , coincidence detection in neurobiology , barn owl , sound localization , electrophysiology , auditory system , cochlear nucleus , auditory cortex , pathology , medicine , paleontology , alternative medicine , predation , coincidence , stimulation
In the auditory system, precise encoding of temporal information is critical for sound localization, a task with direct behavioral relevance. Interaural timing differences (ITDs) are computed using axonal delay lines and cellular coincidence detectors in nucleus laminaris (NL). We present morphological and physiological data on the timing circuits in the emu, Dromaius novaehollandiae , and compare these results with those from the barn owl ( Tyto alba ) and the domestic chick ( Gallus gallus ). Emu NL was composed of a compact monolayer of bitufted neurons whose two thick primary dendrites were oriented dorsoventrally. They showed a gradient in dendritic length along the presumed tonotopic axis. The NL and nucleus magnocellularis (NM) neurons were strongly immunoreactive for parvalbumin, a calcium‐binding protein. Antibodies against synaptic vesicle protein 2 and glutamic acid decarboxlyase revealed that excitatory synapses terminated heavily on the dendritic tufts, while inhibitory terminals were distributed more uniformly. Physiological recordings from brainstem slices demonstrated contralateral delay lines from NM to NL. During whole‐cell patch‐clamp recordings, NM and NL neurons fired single spikes and were doubly rectifying. NL and NM neurons had input resistances of 30.0 ± 19.9 MΩ and 49.0 ± 25.6 MΩ, respectively, and membrane time constants of 12.8 ± 3.8 ms and 3.9 ± 0.2 ms. These results provide further support for the Jeffress model for sound localization in birds. The emu timing circuits showed the ancestral (plesiomorphic) pattern in their anatomy and physiology, while differences in dendritic structure compared to chick and owl may indicate specialization for encoding ITDs at low best frequencies. J. Comp. Neurol. 495:185–201, 2006. © 2006 Wiley‐Liss, Inc.