Repetition enhances hearing detection thresholds in a harbour seal (Phoca vitulina)

1993 ◽  
Vol 71 (5) ◽  
pp. 926-932 ◽  
Author(s):  
S. D. Turnbull ◽  
J. M. Terhune
Keyword(s):  
White Noise ◽  
Background Noise ◽  
Phoca Vitulina ◽  
Harbour Seal ◽  
Detection Thresholds ◽  
Noise Masking ◽  
Phoca Groenlandica ◽  
Hearing Thresholds ◽  
Lower Detection ◽  
Pinniped Species

Pure-tone hearing thresholds of a harbour seal (Phoca vitulina) were measured in air and underwater using behavioural psychophysical techniques. A 50-ms sinusoidal pulse was presented in both white-noise masked and unmasked situations at pulse repetition rates of 1, 2, 4, and 10/s. Test frequencies were 0.5, 1.0, 2.0, 4.0, and 8.0 kHz in air and 2.0, 4.0, 8.0, and 16.0 kHz underwater. Relative to 1 pulse/s, mean threshold shifts were −1, −3, and −5 dB at 2, 4, and 10 pulses/s, respectively. The threshold shifts from 1 to 10 pulses/s were significant (F = 12.457, df = 2,36, p < 0.001) and there was no difference in the threshold shifts between the masked and unmasked situations (F = 2.585; df = 1,50; p > 0.10). Broadband masking caused by meteorological or industrial sources will closely resemble the white-noise situation. At high calling rates, the numerous overlapping calls of some species (e.g., harp seal, Phoca groenlandica) present virtually continous "background noise" which also resembles the broadband white-noise masking situation. An implication of lower detection thresholds is that if a seal regularly repeats short vocalizations, the communication range of that call could be increased significantly (80% at 10 pulses/s). This could have important implications during the breeding season should storms or shipping noises occur or when some pinniped species become increasingly vocal and the background noise of conspecifics increases.

Masked and unmasked pure tone detection thresholds of a harbour seal listening in air

1991 ◽  
Vol 69 (8) ◽  
pp. 2059-2066 ◽  
Author(s):  
J. M. Terhune
Keyword(s):  
White Noise ◽  
Pure Tone ◽  
Phoca Vitulina ◽  
Harbour Seal ◽  
Optimal Conditions ◽  
Vascular Changes ◽  
Detection Thresholds ◽  
Noise Masker ◽  
Auditory Systems ◽  
Tone Detection

In-air pure tone detection thresholds of a harbour seal (Phoca vitulina) were measured using behavioural psychophysical techniques. Thresholds dropped from about 70 dB re 20 μPa at 0.1 kHz to about 35 dB re 20 μ Pa at 4 kHz and then increased to about 45 dB re 20 μPa at 16 kHz. Increased sensitivities at 2 and 8 kHz, which have been reported in other pinnipeds, were not evident. In-air intensity detection thresholds averaged 32 dB above their underwater counterparts (1–16 kHz). Masking studies found the critical ratios at 0.25, 0.5, and 1 kHz to be 24, 15, and 21 dB, respectively (white noise masker). From 0.2 to 1.5 kHz, bandwidths 20 dB below the level of pure tone maskers were 0.16–0.18 kHz. Circumstantial evidence suggests the possibility that blood vascular changes associated with diving might also influence the sensitivity of the auditory systems of seals. Under optimal conditions, a pup's airborne cries may be detected by its mother at ranges of 1 km or more.

Changes in masked thresholds of a harbour seal (Phoca vitulina) associated with angular separation of signal and noise sources

1994 ◽  
Vol 72 (11) ◽  
pp. 1863-1866 ◽  
Author(s):  
S. D. Turnbull
Keyword(s):  
White Noise ◽  
Pure Tone ◽  
Noise Source ◽  
Angular Separation ◽  
Phoca Vitulina ◽  
Harbour Seal ◽  
Noise Sources ◽  
Detection Thresholds ◽  
Noise Masker ◽  
Significant Difference

The masked pure tone thresholds of a harbour seal (Phoca vitulina) were measured at various angles using a white noise masker. The white noise source was placed at 0°, 30°, 60°, and 90° relative to the midline of the seal's head (0°). The masked pure tone thresholds for each angle were determined at 2, 4, 8, and 16 kHz. As the angle separating the signal and noise sources increased from 0° to 90°, the critical ratios of the harbour seal decreased by 1–4 dB. This shift in masked thresholds from a reference point of 0° azimuth was significant (H = 10.374, df = 3,16, p < 0.05). No significant difference was found in masked thresholds between 0° and 30° or between 60° and 90°. This indicates that if a noise source is separated by more than 30° relative to the location of a vocalizing seal, signal detection thresholds will be enhanced and communication distances increased.

Detection thresholds of a harbour seal to repeated underwater high-frequency, short-duration sinusoidal pulses

1988 ◽  
Vol 66 (7) ◽  
pp. 1578-1582 ◽  
Author(s):  
J. M. Terhune
Keyword(s):  
High Frequency ◽  
Threshold Energy ◽  
Phoca Vitulina ◽  
Harbour Seal ◽  
Specific Time ◽  
Detection Thresholds ◽  
Time Period ◽  
Hearing Thresholds ◽  
Number Of Cycles ◽  
Underwater Hearing

Underwater hearing thresholds of a harbour seal (Phoca vitulina) were obtained from 1 to 64 kHz using sinusoidal pulses as short as 0.5 ms. The lowest threshold was 57 dB (re 1 μPa) at 8 kHz. Thresholds for 500- to 50-ms tones increased to about 70 dB (re 1 μPa) in the 1- to 4-kHz and 32-kHz ranges and to 111 dB (re 1 μPa) at 64 kHz. At 50 ms duration, thresholds were from 0 to 6 dB greater than the maximum sensitivity for each frequency tested. Thus, only very brief seal vocalizations are not as audible as longer (and equally loud) underwater calls. For pulses shorter than 400 cycles, the thresholds increased linearly with the logarithm of the number of cycles, independent of frequency (4–32 kHz). The total energy of the pulses at threshold was estimated. From 4 to 32 kHz, as the pulse durations shortened, the threshold energy value decreased and then began to increase. These findings bring into question the concept that when presented with high-frequency sound, the auditory system integrates energy for a specific time period.

Effect of Consonant-Vowel Ratio Modification on Amplitude Envelope Cues for Consonant Recognition

1991 ◽  
Vol 34 (2) ◽  
pp. 415-426 ◽  
Author(s):  
Richard L. Freyman ◽  
G. Patrick Nerbonne ◽  
Heather A. Cote
Keyword(s):  
White Noise ◽  
Intensity Ratio ◽  
Recognition Performance ◽  
Amplitude Envelope ◽  
Signal To Noise ◽  
Noise Masking ◽  
Spectral Cues ◽  
Consonant Recognition ◽  
Nonlinear Amplification ◽  
Speech Envelope

This investigation examined the degree to which modification of the consonant-vowel (C-V) intensity ratio affected consonant recognition under conditions in which listeners were forced to rely more heavily on waveform envelope cues than on spectral cues. The stimuli were 22 vowel-consonant-vowel utterances, which had been mixed at six different signal-to-noise ratios with white noise that had been modulated by the speech waveform envelope. The resulting waveforms preserved the gross speech envelope shape, but spectral cues were limited by the white-noise masking. In a second stimulus set, the consonant portion of each utterance was amplified by 10 dB. Sixteen subjects with normal hearing listened to the unmodified stimuli, and 16 listened to the amplified-consonant stimuli. Recognition performance was reduced in the amplified-consonant condition for some consonants, presumably because waveform envelope cues had been distorted. However, for other consonants, especially the voiced stops, consonant amplification improved recognition. Patterns of errors were altered for several consonant groups, including some that showed only small changes in recognition scores. The results indicate that when spectral cues are compromised, nonlinear amplification can alter waveform envelope cues for consonant recognition.

Hearing Thresholds of Two Harbor Seals (Phoca vitulina) for Helicopter Dipping Sonar Signals (1.3-1.4 kHz)

2019 ◽  
Vol 45 (3) ◽  
pp. 349-355
Author(s):  
Ronald A. Kastelein ◽  
Robin Gransier ◽  
Marloe Brouwers ◽  
Lean Helder-Hoek
Keyword(s):  
Phoca Vitulina ◽  
Harbor Seals ◽  
Hearing Thresholds

Effect of Contralateral White Noise Masking on the Mismatch Negativity

1995 ◽  
Vol 24 (3) ◽  
pp. 165-173 ◽  
Author(s):  
Sirkku K. Salo ◽  
A. Heikki Lang ◽  
Altti J. Salmivalli
Keyword(s):  
White Noise ◽  
Mismatch Negativity ◽  
Noise Masking

Vitamin A physiology in the precocious harbour seal (Phoca vitulina): a tissue-based biomarker approach

2002 ◽  
Vol 80 (9) ◽  
pp. 1511-1519 ◽  
Author(s):  
Lizzy Mos ◽  
Peter S Ross
Keyword(s):  
Vitamin A ◽  
Marine Mammals ◽  
Relevant Information ◽  
Phoca Vitulina ◽  
Retinyl Palmitate ◽  
Harbour Seal ◽  
Natural Processes ◽  
Reproductive Endocrine ◽  
Positive Correlations ◽  
Free Ranging

Vitamin A is a nutrient essential to all mammals for growth and development, as well as for the maintenance of reproductive, endocrine, and immune systems. Environmental contaminant-related disruption of vitamin A has been observed in many wildlife species and can therefore be used as a biomarker of toxic effects. However, the natural processes regulating vitamin A uptake, storage, and distribution among compartments are poorly understood in marine mammals. In this study, 20 young healthy harbour seals (Phoca vitulina) were captured to establish a compartment-based model providing a foundation for a mechanistic understanding of vitamin A physiology and disruption. Vitamin A (retinol, retinyl palmitate, and (or) retinoic acid) was quantified in blood plasma and in biopsy samples of liver, blubber, and skin. Although the highest concentrations of vitamin A were found in liver, blubber represents a more important storage depot, with an estimated 66% of the total retinoid content of the compartments measured. We suggest that vitamin A physiology in the precocious harbour seal has evolved to deal with high vitamin A availability during a short nursing period and to sustain growth during the postweaning fast. Positive correlations in vitamin A concentrations among liver, blubber, and skin support the use of less invasive biopsy sampling of just blubber or skin, which can provide physiologically relevant information in biomarker studies of free-ranging marine mammals.

The effect of different lower detection thresholds in microdosimetric spectra and their mean values

2021 ◽  
pp. 106626
Author(s):  
A. Bianchi ◽  
A. Selva ◽  
P. Colautti ◽  
A. Parisi ◽  
F. Vanhavere ◽  
...  
Keyword(s):  
Detection Thresholds ◽  
Mean Values ◽  
Lower Detection

Bipolar or rectified chromatic detection mechanisms?

2001 ◽  
Vol 18 (1) ◽  
pp. 127-135 ◽  
Author(s):  
MARCEL J. SANKERALLI ◽  
KATHY T. MULLEN
Keyword(s):  
Color Vision ◽  
Masking Effect ◽  
Yellow Light ◽  
Detection Thresholds ◽  
Noise Masking ◽  
Human Color Vision ◽  
Early Processing ◽  
The Cross ◽  
On And Off Pathways ◽  
Luminance Increment

It is widely accepted that human color vision is based on two types of cone-opponent mechanism, one differencing L and M cone types (loosely termed “red–green”), and the other differencing S with the L and M cones (loosely termed “blue–yellow”). The traditional view of the early processing of human color vision suggests that each of these cone-opponent mechanisms respond in a bipolar fashion to signal two opponent colors (red vs. green, blue vs. yellow). An alternative possibility is that each cone-opponent response, as well as the luminance response, is rectified, so producing separable signals for each pole (red, green, blue, yellow, light, and dark). In this study, we use psychophysical noise masking to determine whether the rectified model applies to detection by the postreceptoral mechanisms. We measured the contrast-detection thresholds of six test stimuli (red, green, blue, yellow, light, and dark), corresponding to the two poles of each of the three postreceptoral mechanisms. For each test, we determined whether noise presented to the cross pole had the same masking effect as noise presented to the same pole (e.g. comparing masking of luminance increments by luminance decrement noise (cross pole) and luminance increment noise (same pole)). To avoid stimulus cancellation, the test and mask were presented asynchronously in a “sandwich” arrangement (mask-test-mask). For the six test stimuli, we observed that noise masks presented to the cross pole did not raise the detection thresholds of the test, whereas noise presented to the same pole produced a substantial masking. This result suggests that each color signal (red, green, blue, and yellow) and luminance signal (light and dark) is subserved by a separable mechanism. We suggest that the cone-opponent and luminance mechanisms have similar physiological bases, since a functional separation of the processing of cone increments and cone decrements could underlie both the separation of the luminance system into ON and OFF pathways as well as the splitting of the cone-opponent mechanisms into separable color poles.

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