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

Time-scarcity, ready-meals, ill-health and the obesity epidemic

In this 3-part paper, we firstly review the interaction of time-scarcity with food-choices, specifically ready-meals, and potential health consequences from their consumption. Secondly we review declared nutrients, in relation to the standard 30% of Guideline Daily Amounts, concluding that popular ready-meals from major UK supermarkets are currently nutritionally haphazard. Thirdly, we present a simple scheme to establish standards for nutritional composition of ready-meals: unless otherwise specified, any meal (the smallest unit of nutrition) as recommended to be eaten or as offered should provide 30%+10% of GDA for energy and pro rata for key nutrients (e.g. sodium, sat fat, vitamin C)

Extracellular vesicles generated by placental tissues ex vivo: A transport system for immune mediators and growth factors

Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/144634/1/aji12860_am.pdfhttps://deepblue.lib.umich.edu/bitstream/2027.42/144634/2/aji12860.pdfhttps://deepblue.lib.umich.edu/bitstream/2027.42/144634/3/aji12860-sup-0001-Supinfo.pd

Frequency of greatest temporary hearing threshold shift in harbor seals (Phoca vitulina) depends on fatiguing sound level

Harbor seals may suffer hearing loss due to intense sounds. After exposure for 60 min to a continuous 6.5 kHz tone at sound pressure levels of 123-159 dB re 1 µPa, resulting in sound exposure levels (SELs) of 159-195 dB re 1 μPa2s, temporary threshold shifts (TTSs) in two harbor seals were quantified at the center frequency of the fatiguing sound (6.5 kHz) and at 0.5 and 1.0 octaves above that frequency (9.2 and 13.0 kHz) by means of a psychoacoustic technique. Taking into account the different timing of post-exposure hearing tests, susceptibility to TTS was similar in both animals. The higher the SEL, the higher the TTS induced at frequencies above the fatiguing sound's center frequency. Below ∼179 dB re 1 μPa2s, the maximum TTS was at the center frequency (6.5 kHz); above ∼179 dB re 1 μPa2s, the maximum TTS was at half an octave above the center frequency (9.2 kHz). These results should be considered when interpreting previous TTS studies, and when estimating ecological impacts of anthropogenic sound on the hearing and ecology of harbor seals. Based on the results of the present study and previous studies, harbor seal hearing, in the frequency range 2.5-6.5 kHz, appears to be approximately equally susceptible to TTS.status: publishe

Underwater hearing sensitivity of harbor seals (Phoca vitulina) for narrow noise bands between 0.2 and 80 kHz

The underwater hearing sensitivities of two 1.5-year-old female harbor seals were quantified in a quiet pool built specifically for acoustic research, by using a behavioral psychoacoustic technique. The animals were trained to respond when they detected an acoustic signal and not to respond when they did not ("go/no-go" response). Fourteen narrowband noise signals (1/3-octave bands but with some energy in adjacent bands), at 1/3-octave center frequencies of 0.2-80 kHz, and of 900 ms duration, were tested. Thresholds at each frequency were measured using the up-down staircase method and defined as the stimulus level resulting in a 50% detection rate. Between 0.5 and 40 kHz, the thresholds corresponded to a 1/3-octave band noise level of ∼60 dB re 1 μPa (SD±3.0 dB). At lower frequencies, the thresholds increased to 66 dB re 1 μPa and at 80 kHz the thresholds rose to 114 dB re 1 μPa. The 1/3-octave noise band thresholds of the two seals did not differ from each other, or from the narrowband frequency-modulated tone thresholds at the same frequencies obtained a few months before for the same animals. These hearing threshold values can be used to calculate detection ranges of underwater calls and anthropogenic noises by harbor seals.</p

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