Publications by authors named "Curtis Mobley"

While the effects of irradiance on coral productivity are well known, corals along a shallow to mesophotic depth gradient (10-100 m) experience incident irradiances determined by the optical properties of the water column, coral morphology, and reef topography.Modeling of productivity (i.e.

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Sunburn at the seaside.

Photodermatol Photoimmunol Photomed

September 2018

Background/purpose: The purpose of this paper is to estimate the contribution to our erythemal exposure at the coast of solar ultraviolet (UV) both reflected from, and transmitted into, the ocean.

Methods: The reflection of solar UV radiation from, and transmitted into, seawater was calculated using a numerical model under a number of atmospheric conditions to estimate erythemal exposure on the skin of supine/prone and ambulant people.

Results: The results were expressed as UV Indices.

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Atmospheric and oceanic radiative transfer models were used to compute spectral radiances between 285 and 400 nm onto horizontal and vertical plane surfaces over water. The calculations kept track of the contributions by the sun's direct beam, by diffuse-sky radiance, by radiance reflected from the sea surface and by water-leaving radiance. Clear, hazy and cloudy sky conditions were simulated for a range of solar zenith angles, wind speeds and atmospheric ozone concentrations.

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The evolution of terrestrial vertebrates, starting around 385 million years ago, is an iconic moment in evolution that brings to mind images of fish transforming into four-legged animals. Here, we show that this radical change in body shape was preceded by an equally dramatic change in sensory abilities akin to transitioning from seeing over short distances in a dense fog to seeing over long distances on a clear day. Measurements of eye sockets and simulations of their evolution show that eyes nearly tripled in size just before vertebrates began living on land.

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The diffuse attenuation coefficient K(λ) was first expressed in terms of the inherent optical properties (IOPs) of water according to well-established empirical bio-optical models. Boltzmann simulated annealing was then used to find the best sets of IOPs to fit K(λ) spectra to the reference spectra Kd0(λ) that define the Jerlov water types. Absorption a(λ) and scattering b(λ) coefficients were thus obtained for all Jerlov water types over the wavelength range 300-700 nm.

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Generation of random sea surfaces using wave variance spectra and Fourier transforms is formulated in a way that guarantees conservation of wave energy and fully resolves wave height and slope variances. Monte Carlo polarized ray tracing, which accounts for multiple scattering between light rays and wave facets, is used to compute effective Mueller matrices for reflection and transmission of air- or water-incident polarized radiance. Irradiance reflectances computed using a Rayleigh sky radiance distribution, sea surfaces generated with Cox-Munk statistics, and unpolarized ray tracing differ by 10%-18% compared with values computed using elevation- and slope-resolving surfaces and polarized ray tracing.

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An inverse algorithm is developed to retrieve hyperspectral absorption and backscattering coefficients from measurements of hyperspectral upwelling radiance and downwelling irradiance in vertically homogeneous waters. The forward model is the azimuthally averaged radiative transfer equation, efficiently solved by the EcoLight radiative transfer model, which includes the effects of inelastic scattering. Although this inversion problem is ill posed (the solution is ambiguous for retrieval of total scattering coefficients), unique and stable solutions can be found for absorption and backscattering coefficients.

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Accurate calculation of underwater light is fundamental to predictions of upper-ocean heating, primary production, and photo-oxidation. However, most ocean models simulating these processes do not yet incorporate radiative transfer modules for their light calculations. Such models are often driven by above-surface, broadband, daily averaged irradiance or photosynthetically available radiation (PAR) values obtained from climatology or satellite observations, sometimes without correction for sea-surface reflectance, even though surface reflectance can reduce in-water values by more than 20%.

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Ocean physical-biological-optical ecosystem models can require light calculations at thousands of grid points and time steps. Implicit inverse models that recover ocean absorption and scattering properties from measured light variables can require thousands of solutions of the radiative transfer equation. An extremely fast radiative transfer code, EcoLight-S(ubroutine), has been developed to address these needs.

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Using hyperspectral measurements made in the field, we show that the effective sea-surface reflectance ρ (defined as the ratio of the surface-reflected radiance at the specular direction corresponding to the downwelling sky radiance from one direction) varies not only for different measurement scans, but also can differ by a factor of 8 between 400 nm and 800 nm for the same scan. This means that the derived water-leaving radiance (or remote-sensing reflectance) can be highly inaccurate if a spectrally constant ρ value is applied (although errors can be reduced by carefully filtering measured raw data). To remove surface-reflected light in field measurements of remote sensing reflectance, a spectral optimization approach was applied, with results compared with those from remote-sensing models and from direct measurements.

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A spectrum-matching and look-up-table (LUT) methodology has been developed and evaluated to extract environmental information from remotely sensed hyperspectral imagery. The LUT methodology works as follows. First, a database of remote-sensing reflectance (Rrs) spectra corresponding to various water depths, bottom reflectance spectra, and water-column inherent optical properties (IOPs) is constructed using a special version of the HydroLight radiative transfer numerical model.

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Many deep-sea species, particularly crustaceans, cephalopods, and fish, use photophores to illuminate their ventral surfaces and thus disguise their silhouettes from predators viewing them from below. This strategy has several potential limitations, two of which are examined here. First, a predator with acute vision may be able to detect the individual photophores on the ventral surface.

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We present three methods for deriving water-leaving radiance L(w)(lambda) and remote-sensing reflectance using a hyperspectral tethered spectral radiometer buoy (HyperTSRB), profiled spectroradiometers, and Hydrolight simulations. Average agreement for 53 comparisons between HyperTSRB and spectroradiometric determinations of L(w)(lambda) was 26%, 13%, and 17% at blue, green, and red wavelengths, respectively. Comparisons of HyperTSRB (and spectroradiometric) L(w)(lambda) with Hydrolight simulations yielded percent differences of 17% (18%), 17% (18%), and 13% (20%) for blue, green, and red wavelengths, respectively.

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Numerical simulations show that underwater radiances, irradiances, and reflectances are sensitive to the shape of the scattering phase function at intermediate and large scattering angles, although the exact shape of the phase function in the backscatter directions (for a given backscatter fraction) is not critical if errors of the order of 10% are acceptable. We present an algorithm for generating depth- and wavelength-dependent Fournier-Forand phase functions having any desired backscatter fraction. Modeling of a comprehensive data set of measured inherent optical properties and radiometric variables shows that use of phase functions with the correct backscatter fraction and overall shape is crucial to achieve model-data closure.

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