Organic alkalinity in shallow habitats of San Francisco Estuary

Estuaries are prone to increasing acidification due to growing population and urbanization in addition to global climate change. Acidification is largely studied through measuring or calculating carbonate chemistry parameters (dissolved inorganic carbon, pCO2, pH, total alkalinity), therefore a robu...

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Main Author: Shea Hunter Grady
Other Authors: Tomoko Komada, Ellen Hines, Karina Nielsen
Format: Master Thesis
Language:English
Published: San Francisco State University 2023
Subjects:
Online Access:https://hdl.handle.net/20.500.12680/6h4411181
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spelling ftcalifstateuniv:oai:scholarworks:6h4411181 2024-09-30T14:40:50+00:00 Organic alkalinity in shallow habitats of San Francisco Estuary Shea Hunter Grady Tomoko Komada Ellen Hines Karina Nielsen 2023 https://hdl.handle.net/20.500.12680/6h4411181 English eng San Francisco State University Science & Engineering Interdisciplinary Marine and Estuarine Sciences http://hdl.handle.net/20.500.12680/6h4411181 Copyright by Shea Hunter Grady 2023 Masters Thesis 2023 ftcalifstateuniv https://doi.org/20.500.12680/6h4411181 2024-09-10T17:06:14Z Estuaries are prone to increasing acidification due to growing population and urbanization in addition to global climate change. Acidification is largely studied through measuring or calculating carbonate chemistry parameters (dissolved inorganic carbon, pCO2, pH, total alkalinity), therefore a robust understanding of site carbonate chemistry is key to properly assessing habitat vulnerability to instances of acidification. A challenge in doing ocean acidification (OA) work in estuaries is that in contrast to offshore marine settings, carbonate chemistry in estuaries is more dynamic, varying both spatially and temporally. Carbonate chemistry in estuaries is also more compositionally complex, because of relatively high levels of organic alkalinity (AORG). AORG is normally deemed negligible in marine settings, but it is higher in nearshore environments due to dissolved organic matter inputs from sources such as intertidal salt marshes and terrestrial runoff. Challenges associated with quantifying AORG, and the inherent molecular complexity of AORG, have resulted in very little data in existence and a lot remains unknown pertaining to its prevalence in estuaries. To address this knowledge gap, we conducted a first-order investigation of AORG within shallow habitats of the San Francisco Estuary (SFE) to document how AORG varies spatially and temporally with pH and total alkalinity (TA). In four distinct sites (deep main channel, shallow eelgrass embayment, mudflat, and tidal creek) AORG ranged from non-detectable to 189 µmol/kg, which are comparable to AORG values reported for similar sites in the United States North and Southeast. Calculating pCO2 and saturation states of aragonite and calcite by assuming that AORG is absent resulted in an overestimation of these values as AORG (contributing to TA) ranges ~10%. Our findings show that AORG should be taken into consideration to make accurate carbonate chemistry calculations in estuarine settings. https://doi.org/10.46569/6h4411181 Master Thesis Ocean acidification Scholarworks from California State University
institution Open Polar
collection Scholarworks from California State University
op_collection_id ftcalifstateuniv
language English
description Estuaries are prone to increasing acidification due to growing population and urbanization in addition to global climate change. Acidification is largely studied through measuring or calculating carbonate chemistry parameters (dissolved inorganic carbon, pCO2, pH, total alkalinity), therefore a robust understanding of site carbonate chemistry is key to properly assessing habitat vulnerability to instances of acidification. A challenge in doing ocean acidification (OA) work in estuaries is that in contrast to offshore marine settings, carbonate chemistry in estuaries is more dynamic, varying both spatially and temporally. Carbonate chemistry in estuaries is also more compositionally complex, because of relatively high levels of organic alkalinity (AORG). AORG is normally deemed negligible in marine settings, but it is higher in nearshore environments due to dissolved organic matter inputs from sources such as intertidal salt marshes and terrestrial runoff. Challenges associated with quantifying AORG, and the inherent molecular complexity of AORG, have resulted in very little data in existence and a lot remains unknown pertaining to its prevalence in estuaries. To address this knowledge gap, we conducted a first-order investigation of AORG within shallow habitats of the San Francisco Estuary (SFE) to document how AORG varies spatially and temporally with pH and total alkalinity (TA). In four distinct sites (deep main channel, shallow eelgrass embayment, mudflat, and tidal creek) AORG ranged from non-detectable to 189 µmol/kg, which are comparable to AORG values reported for similar sites in the United States North and Southeast. Calculating pCO2 and saturation states of aragonite and calcite by assuming that AORG is absent resulted in an overestimation of these values as AORG (contributing to TA) ranges ~10%. Our findings show that AORG should be taken into consideration to make accurate carbonate chemistry calculations in estuarine settings. https://doi.org/10.46569/6h4411181
author2 Tomoko Komada
Ellen Hines
Karina Nielsen
format Master Thesis
author Shea Hunter Grady
spellingShingle Shea Hunter Grady
Organic alkalinity in shallow habitats of San Francisco Estuary
author_facet Shea Hunter Grady
author_sort Shea Hunter Grady
title Organic alkalinity in shallow habitats of San Francisco Estuary
title_short Organic alkalinity in shallow habitats of San Francisco Estuary
title_full Organic alkalinity in shallow habitats of San Francisco Estuary
title_fullStr Organic alkalinity in shallow habitats of San Francisco Estuary
title_full_unstemmed Organic alkalinity in shallow habitats of San Francisco Estuary
title_sort organic alkalinity in shallow habitats of san francisco estuary
publisher San Francisco State University
publishDate 2023
url https://hdl.handle.net/20.500.12680/6h4411181
genre Ocean acidification
genre_facet Ocean acidification
op_relation http://hdl.handle.net/20.500.12680/6h4411181
op_rights Copyright by Shea Hunter Grady 2023
op_doi https://doi.org/20.500.12680/6h4411181
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