Mapping the Present to Recognize the Future: the Magnitude and Frequency of pH and ΩAr Variability in Washington State

Presentation Abstract

Although the chemistry of ocean acidification (OA) is well understood, observing pH declines in the coastal zone remains a challenge due to the high-magnitude, high-frequency, and irregular pH variations caused by local processes (natural and anthropogenic), which have a significantly larger signal than the global carbon dioxide (CO2) forcing over short timescales. In addition, the dynamic processes common to nearshore environments make it challenging to identify normal carbonate chemistry conditions from a small number of observations. As a result, baseline information for surface ocean pH and other OA relevant parameters, such as aragonite saturation state (ΩAr), is often unavailable in the coastal zone. The lack of modern baseline information challenges our ability to better understand OA in these environments and hampers the ability of decision-making institutions to confidently identify pH-impaired water bodies under the Clean Water Act, which may be necessary to effectively impose conservation measures. To address this issue, we have developed a Washington-specific empirical relationship between salinity and total alkalinity (TA) and have calculated surface ocean pH and ΩAr throughout Washington State’s coastal marine surface waters using estimates of TA paired with in situ CO2 observations from moorings and ships. By compiling and leveraging all of the available surface ocean CO2 observations collected between 1985 and 2015 within Washington waters, we have been able to develop regionally-specific seasonal climatologies of pH, ΩAr, and other OA relevant parameters, providing the first baseline maps for OA in the coastal zone. In addition, three-hour observations of CO2 from four surface moorings in the state are used to evaluate higher-frequency variability and validate the broader regional climatologies. Finally, we use this information to outline strategic monitoring recommendations for detecting OA in Washington, and provide new interpretations of coastal carbonate chemistry variability that will inform future biological OA research in the Pacific Northwest.

Session Title

Ocean Acidification in the Salish Sea

Conference Track

Climate Change and Ocean Acidification

Conference Name

Salish Sea Ecosystem Conference (2016 : Vancouver, B.C.)

Document Type

Event

Start Date

2016 12:00 AM

End Date

2016 12:00 AM

Location

2016SSEC

Type of Presentation

Oral

Genre/Form

conference proceedings; presentations (communicative events)

Contributing Repository

Digital content made available by University Archives, Heritage Resources, Western Libraries, Western Washington University.

Subjects – Topical (LCSH)

Ocean acidification--Northwest, Pacific; Seawater--Sampling--Northwest, Pacific; Seawater--Carbon content--Northwest, Pacific

Geographic Coverage

Salish Sea (B.C. and Wash.); Northwest, Pacific

Rights

This resource is displayed for educational purposes only and may be subject to U.S. and international copyright laws. For more information about rights or obtaining copies of this resource, please contact University Archives, Heritage Resources, Western Libraries, Western Washington University, Bellingham, WA 98225-9103, USA (360-650-7534; heritage.resources@wwu.edu) and refer to the collection name and identifier. Any materials cited must be attributed to the Salish Sea Ecosystem Conference Records, University Archives, Heritage Resources, Western Libraries, Western Washington University.

Type

Text

Language

English

Format

application/pdf

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Mapping the Present to Recognize the Future: the Magnitude and Frequency of pH and ΩAr Variability in Washington State

2016SSEC

Although the chemistry of ocean acidification (OA) is well understood, observing pH declines in the coastal zone remains a challenge due to the high-magnitude, high-frequency, and irregular pH variations caused by local processes (natural and anthropogenic), which have a significantly larger signal than the global carbon dioxide (CO2) forcing over short timescales. In addition, the dynamic processes common to nearshore environments make it challenging to identify normal carbonate chemistry conditions from a small number of observations. As a result, baseline information for surface ocean pH and other OA relevant parameters, such as aragonite saturation state (ΩAr), is often unavailable in the coastal zone. The lack of modern baseline information challenges our ability to better understand OA in these environments and hampers the ability of decision-making institutions to confidently identify pH-impaired water bodies under the Clean Water Act, which may be necessary to effectively impose conservation measures. To address this issue, we have developed a Washington-specific empirical relationship between salinity and total alkalinity (TA) and have calculated surface ocean pH and ΩAr throughout Washington State’s coastal marine surface waters using estimates of TA paired with in situ CO2 observations from moorings and ships. By compiling and leveraging all of the available surface ocean CO2 observations collected between 1985 and 2015 within Washington waters, we have been able to develop regionally-specific seasonal climatologies of pH, ΩAr, and other OA relevant parameters, providing the first baseline maps for OA in the coastal zone. In addition, three-hour observations of CO2 from four surface moorings in the state are used to evaluate higher-frequency variability and validate the broader regional climatologies. Finally, we use this information to outline strategic monitoring recommendations for detecting OA in Washington, and provide new interpretations of coastal carbonate chemistry variability that will inform future biological OA research in the Pacific Northwest.