Normal audiogram but poor sensitivity to brief sounds in mice with compromised voltage-gated sodium channels (Scn8amedJ).

The Scn8amedJ mutation of the gene for sodium channels at the nodes of Ranvier slows nerve conduction, resulting in motor abnormalities. This mutation is also associated with loss of spontaneous bursting activity in the dorsal cochlear nucleus. However initial tests of auditory sensitivity in mice homozygous for this mutation, using standard 400-ms tones, demonstrated normal hearing sensitivity. Further testing, reported here, revealed a severely compromised sensitivity to short-duration tones of 10 and 2 ms durations. Such a deficit might be expected to interfere with auditory functions that depend on rapid processing of auditory signals.

Hearing in alpacas (Vicugna pacos): audiogram, localization acuity, and use of binaural locus cues.

Behavioral audiograms and sound localization abilities were determined for three alpacas (Vicugna pacos). Their hearing at a level of 60 dB sound pressure level (SPL) (re 20 µPa) extended from 40 Hz to 32.8 kHz, a range of 9.7 octaves. They were most sensitive at 8 kHz, with an average threshold of -0.5 dB SPL. The minimum audible angle around the midline for 100-ms broadband noise was 23°, indicating relatively poor localization acuity and potentially supporting the finding that animals with broad areas of best vision have poorer sound localization acuity. The alpacas were able to localize low-frequency pure tones, indicating that they can use the binaural phase cue, but they were unable to localize pure tones above the frequency of phase ambiguity, thus indicating complete inability to use the binaural intensity-difference cue. In contrast, the alpacas relied on their high-frequency hearing for pinna cues; they could discriminate front-back sound sources using 3-kHz high-pass noise, but not 3-kHz low-pass noise. These results are compared to those of other hoofed mammals and to mammals more generally.

Audiogram of the chicken (Gallus gallus domesticus) from 2 Hz to 9 kHz.

The pure-tone thresholds of four domestic female chickens were determined from 2 Hz to 9 kHz using the method of conditioned suppression/avoidance. At a level of 60 dB sound pressure level (re 20 µN/m(2)), their hearing range extends from 9.1 Hz to 7.2 kHz, with a best sensitivity of 2.6 dB at 2 kHz. Chickens have better sensitivity than humans for frequencies below 64 Hz; indeed, their sensitivity to infrasound exceeds that of the homing pigeon. However, when threshold testing moved to the lower frequencies, the animals required additional training before their final thresholds were obtained, suggesting that they may perceive frequencies below 64 Hz differently than higher frequencies.

Hearing in American leaf-nosed bats. IV: the Common vampire bat, Desmodus rotundus.

We behaviorally determined the audiograms of three Common vampire bats (Phyllostomidae, Desmodus rotundus), a species specialized to exist exclusively on blood. The bats were trained to respond to pure tones in a conditioned suppression/avoidance procedure for a blood reward and a mild punisher for failures to detect the tones. Common vampire bats have a hearing range from 716 Hz to 113 kHz at a level of 60 dB. Their best hearing is at 20 kHz where they are slightly more sensitive than other bats, and they have a second peak of good sensitivity at 71 kHz. They have unusually good sensitivity to low frequencies compared to other bats, but are less sensitive to low frequencies than most mammals. Selective pressures affecting high-frequency hearing in bats and mammals in general are discussed.

Use of binaural cues for sound localization in large and small non-echolocating bats: Eidolon helvum and Cynopterus brachyotis.

The authors determined the ability of two old-world non-echolocating bats, Eidolon helvum and Cynopterus brachyotis, to use binaural time and intensity difference cues for localization. The bats were trained to localize pure tones throughout most of their hearing range from loudspeakers located 30 degrees to the left and right of midline. Both species easily localized high frequency tones, indicating they could use the interaural intensity difference cue. However, neither was able to localize low frequency tones even when the tones were amplitude modulated thereby indicating that they could not use ongoing phase difference cues. The authors now know of eight mammals that do not use binaural phase cues for localization, and some possible reasons for this inability are explored.

Tinnitus and hearing loss in hamsters (Mesocricetus auratus) exposed to loud sound.

Hamsters were trained to go left and right to sounds on their left and right sides, respectively. Silent trials were occasionally given in which no sound was presented. Hamsters exposed to a loud 2- or 10-kHz tone in 1 ear often shifted their responding on the silent trials to the side of the exposed ear, suggesting that they perceived a sound in that ear (i.e., tinnitus). The degree of tinnitus was related to the degree of the accompanying hearing loss (estimated by the auditory brainstem response). However, a conductive hearing loss (plugging 1 ear) did not cause a hamster to test positive for tinnitus. Tinnitus could be demonstrated within minutes following tone exposure, indicating an immediate onset, as occurs in humans.