Oceanographic lidar can provide remote estimates of the vertical
distribution of suspended particles in natural waters, potentially
revolutionizing our ability to characterize marine ecosystems and
properly represent them in models of upper ocean biogeochemistry.
However, lidar signals exhibit complex dependencies on water column
inherent optical properties (IOPs) and instrument characteristics,
which complicate efforts to derive meaningful biogeochemical
properties from lidar return signals. In this study, we used a
ship-based system to measure the lidar attenuation coefficient (
α
) and linear depolarization ratio (
δ
) across a variety of optically and
biogeochemically distinct water masses, including turbid coastal
waters, clear oligotrophic waters, and calcite rich waters associated
with a mesoscale coccolithophore bloom. Sea surface IOPs were measured
continuously while underway to characterize the response of
α
and
δ
to changes in particle abundance and
composition. The magnitude of
α
was consistent with the diffuse
attenuation coefficient (
K
d
), though the
α
versus
K
d
relationship was nonlinear.
δ
was positively related to the
scattering optical depth and the calcite fraction of backscattering. A
statistical fit to these data suggests that the polarized scattering
properties of calcified particles are distinct and contribute to
measurable differences in the lidar depolarization ratio. A better
understanding of the polarized scattering properties of
coccolithophores and other marine particles will further our ability
to interpret polarized oceanographic lidar measurements and may lead
to new techniques for measuring the material properties of marine
particles remotely.
This study analyzes characteristics of an important alkyl amine species, dimethylamine (DMA), in cloud water over the northwest Atlantic. Data were gathered from the winter and summer 2020 deployments of...
Oceanographic lidar measurements of the linear depolarization ratio, δ, contain information on the bulk characteristics of marine particles that could improve our ability to study ocean biogeochemistry. However, a scarcity of information on the polarized light‐scattering properties of marine particles and the lack of a framework for separating single and multiple scattering effects on δ have hindered the development of polarization‐based retrievals of bulk particle properties. To address these knowledge gaps, we made single scattering measurements of δ for several compositionally and morphologically distinct marine particle assemblages. We then used a bio‐optical model to explore the influence of multiple scattering and particle characteristics on lidar measurements of δ made during an expedition to sample a mesoscale coccolithophore bloom. Laboratory measurements of linear depolarization revealed a complex dependency on particle shape, size, and composition that were consistent with scattering simulations for idealized nonspherical particles. Model results suggested that the variability in δ measured during the field expedition was driven predominantly by shifts in particle concentration rather than their bulk characteristics. However, model estimates of δ improved when calcite particles were represented by a distinct particle class, highlighting the influence of bulk particle properties on δ. To advance polarized lidar retrievals of bulk particle properties and to constrain the uncertainty in satellite lidar retrievals of particulate backscattering, these results point to the need for future efforts to characterize the variability of particulate depolarization in the ocean and to quantify the sensitivity of operational ocean lidar systems to multiple scattering.
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