Galveston Bay and Coastal Ocean Optical-Geochemical Response to Hurricane Harvey From VIIRS Ocean Color.

Dissolved and particulate organic carbon, suspended particulate matter concentrations, and their optical proxies colored dissolved organic matter absorption and backscattering coefficients were studied in Galveston Bay, Texas, following the extreme flooding of Houston and surrounding areas due to Hurricane Harvey (25-29 August 2017) using field and ocean color observations. A three-step empirical-semianalytic algorithm for determination of colored dissolved organic matter absorption and backscattering coefficients revealed the dynamics of dissolved organic carbon and particle distribution from Visible and Infrared Imaging Radiometric Suite ocean color. Environmental drivers, especially floodwater discharge and winds, strongly influenced the spatiotemporal distribution of dissolved/particulate material in the bay and shelf waters following the hurricane passage. Over 10 days during/following the hurricane, ~25.2 × 106 kg C of total organic carbon and ~314.7 × 106 kg of suspended particulate matter were rapidly exported from Galveston Bay (representing ~0.65% and 0.27% of respective annual Mississippi River fluxes to the Gulf of Mexico), with potential for ecological impacts to shelf waters.

Changing Dynamics of Dissolved Organic Matter Fluorescence in the Northern Gulf of Mexico Following the Deepwater Horizon Oil Spill.

The characteristics of fluorescent components of dissolved organic matter (DOM) were examined using excitation emission matrix (EEM) fluorescence spectroscopy combined with parallel-factor analysis (PARAFAC) for seawater samples obtained from the northern Gulf of Mexico (NGoM) before, during, and after the 2010 Deepwater Horizon (DwH) oil spill. An EEMs PARAFAC modeling of samples collected within 16 km of the wellhead during the oil spill in May 2010, which included one typical subsurface sample with a PAH concentration of 1.09 µg/L, identified two humic-like and two previously reported oil-like components. Compared to prespill levels, however, there were order-of-magnitude higher fluorescence intensities associated with these components that are consistent with an oil-spill source. The spectral decomposition of the EEMs data using individual and combined data sets from coastal and offshore waters impacted by the DwH spill further revealed the changing nature of fluorescent DOM composition. Although the PAHs concentrations were at prespill conditions after the spill in 2012 and 2013 near the DwH site, the variable and anomalous levels of fluorescence intensities and DOC concentrations three years after the spill suggest the potential long-term persistence of the oil in the DOC pool in the NGoM.

Phytoplankton light absorption of cultures and natural samples: comparisons using two spectrophotometers.

Here we present laboratory measurements of phytoplankton absorption for cultures and natural water samples using two different spectrophotometers, an Ultrapath system and a double beam spectrophotometer equipped with an integrating sphere (Lambda 850). The Ultrapath system provides simplified optics with high throughput efficiency, portability, and is relatively less expensive in comparison to conventional spectrophotometers. A more robust algorithm for correction of pathlength amplification (ß) for particles retained on filter paper was determined for Lambda 850 in comparison to the Ultrapath. The Lambda 850 ß algorithm (ODs(λ) = 0.405 [ODf(λ)] + 0.475 [ODf(λ)]2; r2 = 0.973; n = 7395) showed species and size dependence as indicated by the LISST 100X and HPLC chlorophyll-a concentration data. A better agreement was observed between the two spectrophotometers for filter paper measurements (r2 = 0.991; slope = 0.958; n = 130 for cultures and r2 = 0.978; slope = 0.957; n = 349 for natural samples), than for suspensions (r2 = 0.960; slope = 0.915; n = 92 for cultures and r2 = 0.960; slope = 0.921; n = 27 for natural samples). The differences in measurement of suspensions between the spectrophotometers could be attributed to volume scattering function and acceptance angle of the waveguide detector.

Chromophoric dissolved organic matter (CDOM) variability in Barataria Basin using excitation-emission matrix (EEM) fluorescence and parallel factor analysis (PARAFAC).

Chromophoric dissolved organic matter (CDOM) variability in Barataria Basin, Louisiana, USA,was examined by excitation emission matrix (EEM) fluorescence combined with parallel factor analysis (PARAFAC). CDOM optical properties of absorption and fluorescence at 355nm along an axial transect (36 stations) during March, April, and May 2008 showed an increasing trend from the marine end member to the upper basin with mean CDOM absorption of 11.06 + or - 5.01, 10.05 + or - 4.23, 11.67 + or - 6.03 (m(-)(1)) and fluorescence 0.80 + or - 0.37, 0.78 + or - 0.39, 0.75 + or - 0.51 (RU), respectively. PARAFAC analysis identified two terrestrial humic-like (component 1 and 2), one non-humic like (component 3), and one soil derived humic acid like (component 4) components. The spatial variation of the components showed an increasing trend from station 1 (near the mouth of basin) to station 36 (end member of bay; upper basin). Deviations from this increasing trend were observed at a bayou channel with very high chlorophyll-a concentrations especially for component 3 in May 2008 that suggested autochthonous production of CDOM. The variability of components with salinity indicated conservative mixing along the middle part of the transect. Component 1 and 4 were found to be relatively constant, while components 2 and 3 revealed an inverse relationship for the sampling period. Total organic carbon showed increasing trend for each of the components. An increase in humification and a decrease in fluorescence indices along the transect indicated an increase in terrestrial derived organic matter and reduced microbial activity from lower to upper basin. The use of these indices along with PARAFAC results improved dissolved organic matter characterization in the Barataria Basin.

Short-term Influences on Suspended Particulate Matter Distribution in the Northern Gulf of Mexico: Satellite and Model Observations.

Energetic meteorological events such as frontal passages and hurricanes often impact coastal regions in the northern Gulf of Mexico that influence geochemical processes in the region. Satellite remote sensing data such as winds from QuikSCAT, suspended particulate matter (SPM) concentrations derived from SeaWiFS and the outputs (sea level and surface ocean currents) of a nested navy coastal ocean model (NCOM) were combined to assess the effects of frontal passages between 23-28 March 2005 on the physical properties and the SPM characteristics in the northern Gulf of Mexico. Typical changes in wind speed and direction associated with frontal passages were observed in the latest 12.5 km wind product from QuikSCAT with easterly winds before the frontal passage undergoing systematic shifts in direction and speed and turning northerly, northwesterly during a weak and a strong front on 23 and 27 March, respectively. A quantitative comparison of model sea level results with tide gauge observations suggest better correlations near the delta than in the western part of the Gulf with elevated sea levels along the coast before the frontal passage and a large drop in sea level following the frontal passage on 27 March. Model results of surface currents suggested strong response to wind forcing with westward and onshore currents before the frontal passage reversing into eastward, southeastward direction over a six day period from 23 to 28 March 2005. Surface SPM distribution derived from SeaWiFS ocean color data for two clear days on 23 and 28 March 2005 indicated SPM plumes to be oriented with the current field with increasing concentrations in nearshore waters due to resuspension and discharge from the rivers and bays and its seaward transport following the frontal passage. The backscattering spectral slope γ, a parameter sensitive to particle size distribution also indicated lower γ values (larger particles) in nearshore waters that decreased offshore (smaller particles). The use of both satellite and model results revealed the strong interactions between physical processes and the surface particulate field in response to the frontal passage in a large riverdominated coastal margin.

Bio-optical properties and ocean color algorithms for coastal waters influenced by the Mississippi River during a cold front.

During the passage of a cold front in March 2002, bio-optical properties examined in coastal waters impacted by the Mississippi River indicated that westward advective flows and increasing river discharge containing high concentrations of nonalgal particles contributed significantly to surface optical variability. A comparison of seasonal data from three cruises indicated spectral models of absorption and scattering to be generally consistent with other coastal environments, while their parameterization in terms of chlorophyll (Chl) alpha concentration showed seasonal variability. The exponential slope of the colored dissolved organic matter (CDOM) averaged 0.0161+/-0.00054 nm(-1) and nonalgal absorption averaged 0.011 nm(-1) with deviations from general trends observed due to anomalous water properties. Although the phytoplankton specific absorption coefficients varied over a wide range [0.02 to 0.1 m2 (mg Chl)(-1) at 443 nm] being higher in offshore surface waters, values of phytoplankton absorption spectra at the Sea-Viewing Wide Field-of-View Sensor (SeaWiFS) wave bands were highly correlated to modeled values. Particulate scattering characteristics were similar to observations for other coastal waters, while backscattering ratios were on average lower in phytoplankton-dominated surface waters (0.011+/-0.003) and higher in low Chl near-bottom waters (0.0191+/-0.0045). Average percent differences in remote sensing reflectance Rrs derived from modeled and in-water radiometric measurements were highest in the blue wave bands (52%) and at locations with more stratified water columns. SeaWiFS estimates of Chl and CDOM absorption derived using regional empirical algorithms were highly correlated to in situ data.