Publications by authors named "Brian Hefner"

This study investigates the subsurface sound channel or acoustic duct that appears seasonally along the U.S. Pacific Northwest coast below the surface mixed layer.

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In this paper, a model for the bistatic reverberation associated with seafloor scattering of sound from a moving, narrowband source in an ocean waveguide is developed. Studies of the Doppler effect for moving sources in waveguides have typically focused on the forward propagating field where the Doppler shift leads to a splitting or broadening of the received spectrum. In contrast, the contributions to the scattered field come from all directions and as a consequence the spectrum of the received energy is spread across the entire range of Doppler-shifted frequencies possible for the speed of the source.

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At high frequencies, the attenuation measured in sand sediments is larger than that predicted by Biot theory. To account for this discrepancy, perturbation theory is used to incorporate losses due to scattering by porosity variations into both Biot's poroelastic equations and the effective density fluid model. While previous results showed that fluctuations in the bulk frame modulus were insufficient to produce significant attenuation in a sand sediment, modest levels of fluctuations in the porosity produce significant scattering loss.

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Transducers for acoustic beacons which can produce outgoing signals with wave fronts whose horizontal cross sections are circular or spiral are studied experimentally. A remote hydrophone is used to determine its aspect relative to the transducers by comparing the phase of the circular signal to the phase of the spiral signal. The transducers for a "physical-spiral" beacon are made by forming a strip of 1-3 piezocomposite transducer material around either a circular or spiral backing.

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Downward looking sonar, such as the chirp sonar, is widely used as a sediment survey tool in shallow water environments. Inversion of geo-acoustic parameters from such sonar data precedes the availability of forward models. An exact numerical model is developed to initiate the simulation of the acoustic field produced by such a sonar in the presence of multiple rough interfaces.

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A spiral wave front source generates a pressure field that has a phase that depends linearly on the azimuthal angle at which it is measured. This differs from a point source that has a phase that is constant with direction. The spiral wave front source has been developed for use in navigation; however, very little work has been done to model this source in an ocean environment.

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A spiral wave front source produces an acoustic field that has a phase that is proportional to the azimuthal angle about the source. The concept of a spiral wave front beacon is developed by combining this source with a reference source that has a phase that is constant with the angle. The phase difference between these sources contains information about the receiver's azimuthal angle relative to the beacon and can be used for underwater navigation.

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While Biot theory can successfully account for the dispersion observed in sand sediments, the attenuation at high frequencies has been observed to increase more rapidly than Biot theory would predict. In an effort to account for this additional loss, perturbation theory is applied to Biot's poroelastic equations to model the loss due to the scattering of energy from heterogeneities in the sediment. A general theory for propagation loss is developed and applied to a medium with a randomly varying frame bulk modulus.

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Advancements in automated high-performance thin-layer chromatography (HPTLC) have made it feasible to assess its use for the quantitative analysis of marker compounds in botanical preparations. We report here the findings of method comparisons for the terpenelactones and flavonol aglycones by column high-performance liquid chromatography (HPLC) with evaporative light scattering and UV detection, and HPTLC with a scanning densitometer. For the HPTLC assay of terpenelactones, total bilobalide, ginkgolide A, and ginkgolide B consistently achieved <70% of the total determined using HPLC, regardless of variations to postchromatographic derivatization time and temperature.

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