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Simultaneous Determination of I/Ca and Other Elemental Ratios in Foraminifera: Comparing Results From Acidic and Basic Solutions

The iodine to calcium ratio in carbonate (I/Ca) has been widely used to indicate ocean oxygenation level in the past. Given the volatility of iodine, I/Ca has been measured in alkaline solutions in previous studies. However, this limits the application of I/Ca with other element/Ca (El/Ca) proxies a...

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Published in:Geochemistry, geophysics, geosystems : G3 geophysics, geosystems : G3, 2022-11, Vol.23 (11), p.n/a
Main Authors: Zhou, Xiaoli, Hess, Anya V., Bu, Kaixuan, Sagawa, Takuya, Rosenthal, Yair
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description The iodine to calcium ratio in carbonate (I/Ca) has been widely used to indicate ocean oxygenation level in the past. Given the volatility of iodine, I/Ca has been measured in alkaline solutions in previous studies. However, this limits the application of I/Ca with other element/Ca (El/Ca) proxies at the same time and in the same foraminifera because other El/Ca data are preferably analyzed in acidic solutions. This study assesses the reliability of I/Ca measurements in acidic solutions measured with other El/Ca as well as the effects of different sample pre‐treatments on measured foraminiferal I/Ca. Our results show that when samples are measured within hours of prepaparation, the pH of the final solution has an insignificant effect on I/Ca measurements of a carbonate reference material JCp‐1 and a multi‐element standard solution, consistent with the slow kinetics of iodine volatilization. We find, however, that low pH possibly reduces the measured I/Ca in foraminiferal tests in some samples. Our experiments also suggest a resolvable effect of reductive cleaning, yielding lower foraminiferal I/Ca compared to without reductive cleaning. The HNO3 concentration used to dissolve foraminiferal shells has a negligible effect. Despite the different solution pHs and cleaning and dissolving methods, our core top planktic I/Ca data are able to differentiate well‐oxygenated from oxygen‐depleted waters in the upper ocean, and after correcting for cleaning effect, our data are generally consistent with the published studies that analyzed I/Ca without reductive cleaning and in basic solutions. This study shows that measurements of I/Ca within hours of sample dissolutions yield reliable planktic I/Ca data, while also allowing the acquisition of other El/Ca values for paleoceanographic studies. Plain Language Summary The ratio of chemical elements iodine to calcium (I/Ca) in carbonate has been widely used to indicate the amount of oxygen in modern and ancient oceans. Because iodine is unstable in acidic solutions, I/Ca ratios have been measured in alkaline solutions. However, acquiring I/Ca ratios in this way limits the usage of other element to calcium ratios (El/Ca) that can reflect other physical and chemical properties of the ocean such as temperature and acidity, because these El/Ca ratios are commonly measured in acidic solutions. Here we assess the possibility of producing reliable I/Ca with other El/Ca data in acidic solutions. Our results suggest that I/Ca in fo
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Given the volatility of iodine, I/Ca has been measured in alkaline solutions in previous studies. However, this limits the application of I/Ca with other element/Ca (El/Ca) proxies at the same time and in the same foraminifera because other El/Ca data are preferably analyzed in acidic solutions. This study assesses the reliability of I/Ca measurements in acidic solutions measured with other El/Ca as well as the effects of different sample pre‐treatments on measured foraminiferal I/Ca. Our results show that when samples are measured within hours of prepaparation, the pH of the final solution has an insignificant effect on I/Ca measurements of a carbonate reference material JCp‐1 and a multi‐element standard solution, consistent with the slow kinetics of iodine volatilization. We find, however, that low pH possibly reduces the measured I/Ca in foraminiferal tests in some samples. Our experiments also suggest a resolvable effect of reductive cleaning, yielding lower foraminiferal I/Ca compared to without reductive cleaning. The HNO3 concentration used to dissolve foraminiferal shells has a negligible effect. Despite the different solution pHs and cleaning and dissolving methods, our core top planktic I/Ca data are able to differentiate well‐oxygenated from oxygen‐depleted waters in the upper ocean, and after correcting for cleaning effect, our data are generally consistent with the published studies that analyzed I/Ca without reductive cleaning and in basic solutions. This study shows that measurements of I/Ca within hours of sample dissolutions yield reliable planktic I/Ca data, while also allowing the acquisition of other El/Ca values for paleoceanographic studies. Plain Language Summary The ratio of chemical elements iodine to calcium (I/Ca) in carbonate has been widely used to indicate the amount of oxygen in modern and ancient oceans. Because iodine is unstable in acidic solutions, I/Ca ratios have been measured in alkaline solutions. However, acquiring I/Ca ratios in this way limits the usage of other element to calcium ratios (El/Ca) that can reflect other physical and chemical properties of the ocean such as temperature and acidity, because these El/Ca ratios are commonly measured in acidic solutions. Here we assess the possibility of producing reliable I/Ca with other El/Ca data in acidic solutions. Our results suggest that I/Ca in foraminiferal (single‐celled animal in the ocean) carbonate shells measured in acidic solutions are consistent with those published but measured in alkaline solutions. This confirms the reliability of our new analytical method, which allows measurement of other El/Ca ratios alongside I/Ca. Key Points Analysis of foraminiferal I/Ca in acidic solutions under controlled conditions offers reliable redox proxy estimates Variable sample preparations may affect I/Ca data, but the difference between oxygen‐enriched and oxygen‐depleted waters is maintained</description><identifier>ISSN: 1525-2027</identifier><identifier>EISSN: 1525-2027</identifier><identifier>DOI: 10.1029/2022GC010660</identifier><language>eng</language><publisher>Washington: John Wiley &amp; Sons, Inc</publisher><subject>Acidity ; Analytical methods ; Calcium ; Carbonates ; Chemical elements ; Chemical properties ; Chemicophysical properties ; Cleaning ; Elements ; Foraminifera ; foraminiferal I/Ca ; Iodine ; Kinetics ; method development ; Oceans ; Oxygen ; Oxygenation ; Ratios ; redox proxy ; Reliability ; Shells ; Upper ocean</subject><ispartof>Geochemistry, geophysics, geosystems : G3, 2022-11, Vol.23 (11), p.n/a</ispartof><rights>2022 The Authors.</rights><rights>2022. 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Given the volatility of iodine, I/Ca has been measured in alkaline solutions in previous studies. However, this limits the application of I/Ca with other element/Ca (El/Ca) proxies at the same time and in the same foraminifera because other El/Ca data are preferably analyzed in acidic solutions. This study assesses the reliability of I/Ca measurements in acidic solutions measured with other El/Ca as well as the effects of different sample pre‐treatments on measured foraminiferal I/Ca. Our results show that when samples are measured within hours of prepaparation, the pH of the final solution has an insignificant effect on I/Ca measurements of a carbonate reference material JCp‐1 and a multi‐element standard solution, consistent with the slow kinetics of iodine volatilization. We find, however, that low pH possibly reduces the measured I/Ca in foraminiferal tests in some samples. Our experiments also suggest a resolvable effect of reductive cleaning, yielding lower foraminiferal I/Ca compared to without reductive cleaning. The HNO3 concentration used to dissolve foraminiferal shells has a negligible effect. Despite the different solution pHs and cleaning and dissolving methods, our core top planktic I/Ca data are able to differentiate well‐oxygenated from oxygen‐depleted waters in the upper ocean, and after correcting for cleaning effect, our data are generally consistent with the published studies that analyzed I/Ca without reductive cleaning and in basic solutions. This study shows that measurements of I/Ca within hours of sample dissolutions yield reliable planktic I/Ca data, while also allowing the acquisition of other El/Ca values for paleoceanographic studies. Plain Language Summary The ratio of chemical elements iodine to calcium (I/Ca) in carbonate has been widely used to indicate the amount of oxygen in modern and ancient oceans. Because iodine is unstable in acidic solutions, I/Ca ratios have been measured in alkaline solutions. However, acquiring I/Ca ratios in this way limits the usage of other element to calcium ratios (El/Ca) that can reflect other physical and chemical properties of the ocean such as temperature and acidity, because these El/Ca ratios are commonly measured in acidic solutions. Here we assess the possibility of producing reliable I/Ca with other El/Ca data in acidic solutions. Our results suggest that I/Ca in foraminiferal (single‐celled animal in the ocean) carbonate shells measured in acidic solutions are consistent with those published but measured in alkaline solutions. This confirms the reliability of our new analytical method, which allows measurement of other El/Ca ratios alongside I/Ca. 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Given the volatility of iodine, I/Ca has been measured in alkaline solutions in previous studies. However, this limits the application of I/Ca with other element/Ca (El/Ca) proxies at the same time and in the same foraminifera because other El/Ca data are preferably analyzed in acidic solutions. This study assesses the reliability of I/Ca measurements in acidic solutions measured with other El/Ca as well as the effects of different sample pre‐treatments on measured foraminiferal I/Ca. Our results show that when samples are measured within hours of prepaparation, the pH of the final solution has an insignificant effect on I/Ca measurements of a carbonate reference material JCp‐1 and a multi‐element standard solution, consistent with the slow kinetics of iodine volatilization. We find, however, that low pH possibly reduces the measured I/Ca in foraminiferal tests in some samples. Our experiments also suggest a resolvable effect of reductive cleaning, yielding lower foraminiferal I/Ca compared to without reductive cleaning. The HNO3 concentration used to dissolve foraminiferal shells has a negligible effect. Despite the different solution pHs and cleaning and dissolving methods, our core top planktic I/Ca data are able to differentiate well‐oxygenated from oxygen‐depleted waters in the upper ocean, and after correcting for cleaning effect, our data are generally consistent with the published studies that analyzed I/Ca without reductive cleaning and in basic solutions. This study shows that measurements of I/Ca within hours of sample dissolutions yield reliable planktic I/Ca data, while also allowing the acquisition of other El/Ca values for paleoceanographic studies. Plain Language Summary The ratio of chemical elements iodine to calcium (I/Ca) in carbonate has been widely used to indicate the amount of oxygen in modern and ancient oceans. Because iodine is unstable in acidic solutions, I/Ca ratios have been measured in alkaline solutions. However, acquiring I/Ca ratios in this way limits the usage of other element to calcium ratios (El/Ca) that can reflect other physical and chemical properties of the ocean such as temperature and acidity, because these El/Ca ratios are commonly measured in acidic solutions. Here we assess the possibility of producing reliable I/Ca with other El/Ca data in acidic solutions. Our results suggest that I/Ca in foraminiferal (single‐celled animal in the ocean) carbonate shells measured in acidic solutions are consistent with those published but measured in alkaline solutions. This confirms the reliability of our new analytical method, which allows measurement of other El/Ca ratios alongside I/Ca. Key Points Analysis of foraminiferal I/Ca in acidic solutions under controlled conditions offers reliable redox proxy estimates Variable sample preparations may affect I/Ca data, but the difference between oxygen‐enriched and oxygen‐depleted waters is maintained</abstract><cop>Washington</cop><pub>John Wiley &amp; Sons, Inc</pub><doi>10.1029/2022GC010660</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-7546-6011</orcidid><orcidid>https://orcid.org/0000-0001-9272-2534</orcidid><orcidid>https://orcid.org/0000-0001-8221-9548</orcidid><orcidid>https://orcid.org/0000-0002-1767-9158</orcidid><oa>free_for_read</oa></addata></record>
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subjects Acidity
Analytical methods
Calcium
Carbonates
Chemical elements
Chemical properties
Chemicophysical properties
Cleaning
Elements
Foraminifera
foraminiferal I/Ca
Iodine
Kinetics
method development
Oceans
Oxygen
Oxygenation
Ratios
redox proxy
Reliability
Shells
Upper ocean
title Simultaneous Determination of I/Ca and Other Elemental Ratios in Foraminifera: Comparing Results From Acidic and Basic Solutions
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