Equal latency contours and auditory weighting functions for the harbour porpoise (Phocoena phocoena)

This work was supported by The Netherlands Ministry of Infrastructure and the Environment [grant number 4500182046], and by matched funding from The Netherlands Ministry of Defence (administered by TNO) and the UK Natural Environment Research Council [to P.J.W.].Loudness perception by human infants and animals can be studied under the assumption that sounds of equal loudness elicit equal reaction times (RTs). Simple RTs of a harbour porpoise to narrowband frequency-modulated signals were measured using a behavioural method and an RT sensor based on infrared light. Equal latency contours, which connect equal RTs across frequencies, for reference values of 150-200 ms (10 ms intervals) were derived from median RTs to 1 s signals with sound pressure levels (SPLs) of 59-168 dB re. 1 μPa and centre frequencies of 0.5, 1, 2, 4, 16, 31.5, 63, 80 and 125 kHz. The higher the signal level was above the hearing threshold of the harbour porpoise, the quicker the animal responded to the stimulus (median RT 98-522 ms). Equal latency contours roughly paralleled the hearing threshold at relatively low sensation levels (higher RTs). The difference in shape between the hearing threshold and the equal latency contours was more pronounced at higher levels (lower RTs); a flattening of the contours occurred for frequencies below 63 kHz. Relationships of the equal latency contour levels with the hearing threshold were used to create smoothed functions assumed to be representative of equal loudness contours. Auditory weighting functions were derived from these smoothed functions that may be used to predict perceived levels and correlated noise effects in the harbour porpoise, at least until actual equal loudness contours become available.Publisher PDFPeer reviewe

Equal latency contours and auditory weighting functions for the harbour porpoise (<em>Phocoena phocoena</em>)

Loudness perception by human infants and animals can be studied under the assumption that sounds of equal loudness elicit equal reaction times (RTs). Simple RTs of a harbour porpoise to narrowband frequency-modulated signals were measured using a behavioural method and an RT sensor based on infrared light. Equal latency contours, which connect equal RTs across frequencies, for reference values of 150-200 ms (10 ms intervals) were derived from median RTs to 1 s signals with sound pressure levels (SPLs) of 59-168 dB re. 1 μPa and centre frequencies of 0.5, 1, 2, 4, 16, 31.5, 63, 80 and 125 kHz. The higher the signal level was above the hearing threshold of the harbour porpoise, the quicker the animal responded to the stimulus (median RT 98-522 ms). Equal latency contours roughly paralleled the hearing threshold at relatively low sensation levels (higher RTs). The difference in shape between the hearing threshold and the equal latency contours was more pronounced at higher levels (lower RTs); a flattening of the contours occurred for frequencies below 63 kHz. Relationships of the equal latency contour levels with the hearing threshold were used to create smoothed functions assumed to be representative of equal loudness contours. Auditory weighting functions were derived from these smoothed functions that may be used to predict perceived levels and correlated noise effects in the harbour porpoise, at least until actual equal loudness contours become available.</p

Underwater equal-latency contours of a harbor porpoise (Phocoena phocoena) for tonal signals between 0.5 and 125 kHz

Loudness perception can be studied based on the assumption that sounds of equal loudness elicit equal reaction time (RT; or “response latency”). We measured the underwater RTs of a harbor porpoise to narrowband frequency-modulated sounds and constructed six equal-latency contours. The contours paralleled the audiogram at low sensation levels (high RTs). At high-sensation levels, contours flattened between 0.5 and 31.5 kHz but dropped substantially (RTs shortened) beyond those frequencies. This study suggests that equal-latency-based frequency weighting can emulate noise perception in porpoises for low and middle frequencies but that the RT-loudness correlation is relatively weak for very high frequencies

Temporary Hearing Threshold Shift in Harbor Porpoises (Phocoena phocoena) Due to One-Sixth-Octave Noise Band at 32 kHz

Temporary hearing threshold shift (TTS) caused by fatiguing sounds in the 1.5 to 16 kHz range has been documented in harbor porpoises (Phocoena phocoena). To assess impacts of anthropogenic noise on porpoise hearing, TTS needs to be investigated for other frequencies, as susceptibility appears to depend on the frequency of the fatiguing sound. TTS was quantified after two porpoises (Porpoises F05 and M06) were exposed for 1 hour to a continuous one-sixth-octave noise band centered at 32 kHz, at average received sound pressure levels of 118 to 148 dB re 1 µPa, and at a sound exposure level (SEL) range of 154 to 184 dB re 1 µPa2s. Hearing thresholds for 32, 44.8, and 63 kHz tonal signals were determined before and after exposure to quantify initial TTS and recovery. Porpoise M06’s hearing was tested 1 to 4 min after exposure. At 32 kHz, the lowest SEL that resulted in significant TTS1-4 (3.4 dB) was 166 dB re 1 µPa2s. At 44.8 kHz, the lowest SEL that resulted in significant TTS1-4 (5.2 dB) was 178 dB re 1 µPa2s. The highest TTS1-4 (18.3 dB) occurred at 44.8 kHz after exposure to 184 dB SEL. Porpoise F05’s hearing was tested 12 to 16 min after exposure. At 32 kHz, the lowest SEL that resulted in significant TTS12-16 (3.5 dB) was 184 dB re 1 µPa2s. At 44.8 kHz, the lowest SEL that resulted in significant TTS12-16 (1.2 dB) was 178 dB re 1 µPa2s. The highest TTS12-16 (8.2 dB) occurred in Porpoise F05 at 44.8 kHz after exposure to 184 dB SEL. At 63 kHz, no TTS could be elicited in either animal. Considering that Porpoise F05 had more time than Porpoise M06 for recovery, the susceptibility of the two porpoises to TTS after exposure to sounds of 32 kHz was similar. In the range investigated so far (1.5 to 32 kHz), susceptibility to TTS appears to increase with increasing frequency below ~6.5 kHz, and to decrease with increasing frequency above ~6.5 kHz

Temporary hearing threshold shift in harbor seals (Phoca vitulina) due to a one-sixth-octave noise band centered at 16 kHz

Temporary hearing threshold shifts (TTSs) were investigated in two adult female harbor seals after exposure for 60 min to a continuous one-sixth-octave noise band centered at 16 kHz (the fatiguing sound) at sound pressure levels of 128-149 dB re 1 μPa, resulting in sound exposure levels (SELs) of 164-185 dB re 1 μPas. TTSs were quantified at the center frequency of the fatiguing sound (16 kHz) and at half an octave above that frequency (22.4 kHz) by means of a psychoacoustic hearing test method. Susceptibility to TTS was similar in both animals when measured 8-12 and 12-16 min after cessation of the fatiguing sound. TTS increased with increasing SEL at both frequencies, but above an SEL of 174 dB re 1 μPas, TTS was greater at 22.4 kHz than at 16 kHz for the same SELs. Recovery was rapid: the greatest TTS, measured at 22.4 kHz 1-4 min after cessation of the sound, was 17 dB, but dropped to 3 dB in 1 h, and hearing recovered fully within 2 h. The affected hearing frequency should be considered when estimating ecological impacts of anthropogenic sound on seals. Between 2.5 and 16 kHz the species appears equally susceptible to TTS

Population structure of North Atlantic and North Pacific sei whales (Balaenoptera borealis) inferred from mitochondrial control region DNA sequences and microsatellite genotypes

Currently, three stocks of sei whales (Balaenoptera borealis) are defined in the North Atlantic; the Nova Scotian, Iceland-Denmark Strait and Eastern North Atlantic stocks, which are mainly based upon historical catch and sighting data. We analyzed mitochondrial control region DNA (mtDNA) sequences and genotypes from 7 to 11 microsatellite loci in 87 samples from three sites in the North Atlantic; Iceland, the Gulf of Maine and the Azores, and compared against the North Pacific using 489 previously published samples. No statistically significant deviations from homogeneity were detected among the North Atlantic samples at mtDNA or microsatellite loci. The genealogy estimated from the mtDNA sequences revealed a clear division of the haplotypes into a North Atlantic and a North Pacific clade, with the exception of one haplotype detected in a single sample from the Azores, which was included in the North Pacific clade. Significant genetic divergence between the North Atlantic and North Pacific Oceans was detected (mtDNA ΦST = 0.72, microsatellite Weir and Cockerham’s ϴ = 0.20; p < 0.001). The coalescent-based estimate of the population divergence time between the North Atlantic and North Pacific populations from the sequence variation among the mtDNA sequences was at 163,000 years ago. However, the inference was limited by an absence of samples from the Southern Hemisphere and uncertainty regarding mutation rates and generation times. The estimates of inter-oceanic migration rates were low (Nm at 0.007 into the North Pacific and at 0.248 in the opposite direction). Although estimates of genetic divergence among the current North Atlantic stocks were low and consistent with the extensive range of movement observed in satellite tagged sei whales, the high uncertainty of the genetic divergence estimates precludes rejection of multiple stocks in the North Atlantic.info:eu-repo/semantics/publishedVersio