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1.
J Acoust Soc Am ; 155(3): 2014-2024, 2024 Mar 01.
Article in English | MEDLINE | ID: mdl-38470188

ABSTRACT

Hypoxia in coastal ecosystems is increasing as a result of water quality declines from nutrient pollution. Hypoxia negatively affects fish populations and marine life, limiting their spawning habitats, population size, and growth. In this study, two approaches were used to understand the effect of hypoxia on the chorusing and reproductive behavior of fishes in estuaries. One approach used a water quality meter integrated with a prototype passive acoustic recorder, developed to monitor dissolved oxygen and fish chorusing simultaneously and continuously at sites with normoxic and hypoxic conditions. In a second approach, passive acoustic recorders were deployed near ambient water quality monitoring stations, monitored by the North Carolina agencies in estuaries where hypoxia occurs periodically. In both approaches, when hypoxia (dissolved oxygen < 4.0 mg/L) occurred, fish chorusing was diminished or ceased. A strong correlation was observed between bottom water dissolved oxygen and the power spectral density in a 100-200 Hz frequency band associated with red drum (Sciaenops ocellatus, Sciaenidae) calling. Passive acoustic monitoring stations and integrated passive acoustic and water quality meters should be used in estuarine hypoxia monitoring efforts to examine the expanding areas of hypoxia and its impact on fish critical spawning habitats.


Subject(s)
Ecosystem , Fishes , Animals , Hypoxia , Oxygen , Acoustics
2.
PLoS One ; 17(7): e0267338, 2022.
Article in English | MEDLINE | ID: mdl-35819946

ABSTRACT

Although the continental slope and abyss comprise the largest habitat on earth, the absence of documented fish sounds from deep waters is striking. Fishes with sexually dimorphic muscles attached to their swim bladders suggests that sounds are likely used in male courtship on the upper, mid and lower continental slope. To investigate the effects of environmental extremes on fish sound production, the acoustic behavior of a driven bubble is examined. This study is also relevant to target strength of sonar returns from fish and hearing in auditory specialist fishes. A bubble is a classic, if imperfect, model for swim bladder behavior since the swim-bladder wall is an anisotropic viscoelastic structure responsible for rapid damping. Acoustic properties of bubbles-including far-field resonant frequency, damping factor, and quality factor-are calculated in warm and cold surface conditions and in cold deep-water (depths 1000 m, 2000 m, and 3500 m) conditions using parameters for oxygen and nitrogen, the dominant gases in swim bladders. The far-field resonant frequency and damping factor of a bubble increase with depth, and the scattering cross-section and quality factor decrease with depth. These acoustic properties scale with undamped oscillation frequency of the bubble and do not vary significantly due to gas type or temperature. Bubbles in the deep-water environments are much less efficient radiators of sound than bubbles near the surface because the far-field radiated power for the same excitation decreases with depth. A bubble at depth 3500 m has a 25 dB loss in radiated sound power compared to the same-radius bubble at the surface. This reduction of radiation efficiency in deep water likely contributes to the absence of fish sound recordings in those environments.


Subject(s)
Sound , Water , Acoustics , Animals , Fishes , Gases , Male , Vibration
3.
Adv Exp Med Biol ; 875: 647-53, 2016.
Article in English | MEDLINE | ID: mdl-26611015

ABSTRACT

The question we addressed in this study is whether oyster toadfish respond to vessel disturbances by calling less when vessels with lower frequency spectra are present in a sound recording and afterward. Long-term data recorders were deployed at the Neuse (high vessel-noise site) and Pamlico (low vessel-noise site) Rivers. There were many fewer toadfish detections at the high vessel-noise site than the low-noise station. Calling rates were lower in the high-boat traffic area, suggesting that toadfish cannot call over loud vessel noise, reducing the overall calling rate, and may have to call more often when vessels are not present.


Subject(s)
Batrachoidiformes/physiology , Noise , Ships , Vocalization, Animal/physiology , Animals , Auditory Threshold , North Carolina , Sound Spectrography
4.
Adv Exp Med Biol ; 875: 1089-95, 2016.
Article in English | MEDLINE | ID: mdl-26611072

ABSTRACT

This finite-difference time domain (FDTD) model for sound propagation in very shallow water uses pressure and velocity grids with both 3-dimensional Cartesian and 2-dimensional cylindrical implementations. Parameters, including water and sediment properties, can vary in each dimension. Steady-state and transient signals from discrete and distributed sources, such as the surface of a vibrating pile, can be used. The cylindrical implementation uses less computation but requires axial symmetry. The Cartesian implementation allows asymmetry. FDTD calculations compare well with those of a split-step parabolic equation. Applications include modeling the propagation of individual fish sounds, fish aggregation sounds, and distributed sources.


Subject(s)
Models, Theoretical , Sound , Water , Time Factors
8.
J Acoust Soc Am ; 116(5): 3186-91, 2004 Nov.
Article in English | MEDLINE | ID: mdl-15603164

ABSTRACT

Simultaneous audio and video were recorded of a silver perch Bairdiella chrysoura producing its characteristic drumming sound in the field. The background noise contribution to the total sound pressure level is estimated using sounds that occurred between the pulses of the silver perch sound. This background contribution is subtracted from the total sound to give an estimate of the sound pressure level of the individual fish. A silver perch source level in the range 128-135 dB (re: 1 microPa) is obtained using an estimate of the distance between the fish and the hydrophone. The maximum distance at which an individual silver perch could be detected depends on the background sound level as well as the propagation losses. Under the conditions recorded in this study, the maximum detection distance would be 1-7 m from the hydrophone.


Subject(s)
Perciformes/physiology , Vocalization, Animal/physiology , Air Sacs , Animals , Models, Theoretical , North Carolina , Pressure , Sound , Tape Recording , Videotape Recording
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