Reply to Nicholson's comment on "Consistent calculation of aquatic gross production from oxygen triple isotope measurements" by Kaiser (2011)

The comment by Nicholson (2011a) questions the "consistency" of the "definition" of the "biological end-member" used by Kaiser (2011a) in the calculation of oxygen gross production. "Biological end-member" refers to the relative oxygen isotope ratio differenc...

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Main Authors: J. Kaiser, O. Abe
Format: Article
Language:English
Published: Copernicus Publications 2012-08-01
Series:Biogeosciences
Online Access:http://www.biogeosciences.net/9/2921/2012/bg-9-2921-2012.pdf
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author J. Kaiser
O. Abe
author_facet J. Kaiser
O. Abe
author_sort J. Kaiser
collection DOAJ
description The comment by Nicholson (2011a) questions the "consistency" of the "definition" of the "biological end-member" used by Kaiser (2011a) in the calculation of oxygen gross production. "Biological end-member" refers to the relative oxygen isotope ratio difference between photosynthetic oxygen and Air-O<sub>2</sub> (abbreviated <sup>17</sup>δ<sub>P</sub> and <sup>18</sup>δ<sub>P</sub> for <sup>17</sup>O/<sup>16</sup>O and <sup>18</sup>O/<sup>16</sup>O, respectively). The comment claims that this leads to an overestimate of the discrepancy between previous studies and that the resulting gross production rates are "30% too high". Nicholson recognises the improved accuracy of Kaiser's direct calculation ("dual-delta") method compared to previous approximate approaches based on <sup>17</sup>O excess (<sup>17</sup>Δ) and its simplicity compared to previous iterative calculation methods. Although he correctly points out that differences in the normalised gross production rate (<i>g</i>) are largely due to different input parameters used in Kaiser's "base case" and previous studies, he does not acknowledge Kaiser's observation that iterative and dual-delta calculation methods give exactly the same <i>g</i> for the same input parameters (disregarding kinetic isotope fractionation during air-sea exchange). The comment is based on misunderstandings with respect to the "base case" <sup>17</sup>δ<sub>P</sub> and <sup>18</sup>δ<sub>P</sub> values. Since direct measurements of <sup>17</sup>δ<sub>P</sub> and <sup>18</sup>δ<sub>P</sub>do not exist or have been lost, Kaiser constructed the "base case" in a way that was consistent and compatible with literature data. Nicholson showed that an alternative reconstruction of <sup>17</sup>δ<sub>P</sub> gives <i>g</i> values closer to previous studies. However, unlike Nicholson, we refrain from interpreting either reconstruction as a benchmark for the accuracy of <i>g</i>. A number of publications over the last 12 months have tried to establish which of these two reconstructions is more accurate. Nicholson draws on recently revised measurements of the relative <sup>17</sup>O/<sup>16</sup>O difference between VSMOW and Air-O<sub>2</sub> (<sup>17</sup>δ<sub>VSMOW</sub>; Barkan and Luz, 2011), together with new measurements of photosynthetic isotope fractionation, to support his comment. However, our own measurements disagree with these revised <sup>17</sup>δ<sub>VSMOW</sub> values. If scaled for differences in <sup>18</sup>δ<sub>VSMOW</sub>, they are actually in good agreement with the original data (Barkan and Luz, 2005) and support Kaiser's "base case" <i>g</i> values. The statement that Kaiser's <i>g</i> values are "30% too high" can therefore not be accepted, pending future work to reconcile different <sup>17</sup>δ<sub>VSMOW</sub> measurements. Nicholson also suggests that approximated calculations of gross production should be performed with a triple isotope excess defined as <sup>17</sup>Δ<sup>#</sup>≡ ln (1+<sup>17</sup>δ)–λ ln(1+<sup>18</sup>δ), with λ = θ<sub>R</sub> = ln(1+<sup>17</sup>ϵ<sub>R</sub> ) / ln(1+<sup>18</sup>ϵ<sub>R</sub>). However, this only improves the approximation for certain <sup>17</sup>δ<sub>P</sub> and <sup>18</sup>δ<sub>P</sub> values, for certain net to gross production ratios (<i>f</i>) and for certain ratios of gross production to gross Air-O<sub>2</sub> invasion (<i>g</i>). In other cases, the approximated calculation based on <sup>17</sup>Δ<sup>†</sup> ≡<sup>17</sup>δ – κ <sup>18</sup>δ with κ = γ<sub>R</sub> = <sup>17</sup>ϵ<sub>R</sub>/<sup>18</sup>ϵ<sub>R</sub> (Kaiser, 2011a) gives more accurate results.
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spelling doaj.art-052a2d76834046b19257e53d09b3f9d62022-12-22T00:25:35ZengCopernicus PublicationsBiogeosciences1726-41701726-41892012-08-01982921293310.5194/bg-9-2921-2012Reply to Nicholson's comment on "Consistent calculation of aquatic gross production from oxygen triple isotope measurements" by Kaiser (2011)J. KaiserO. AbeThe comment by Nicholson (2011a) questions the "consistency" of the "definition" of the "biological end-member" used by Kaiser (2011a) in the calculation of oxygen gross production. "Biological end-member" refers to the relative oxygen isotope ratio difference between photosynthetic oxygen and Air-O<sub>2</sub> (abbreviated <sup>17</sup>δ<sub>P</sub> and <sup>18</sup>δ<sub>P</sub> for <sup>17</sup>O/<sup>16</sup>O and <sup>18</sup>O/<sup>16</sup>O, respectively). The comment claims that this leads to an overestimate of the discrepancy between previous studies and that the resulting gross production rates are "30% too high". Nicholson recognises the improved accuracy of Kaiser's direct calculation ("dual-delta") method compared to previous approximate approaches based on <sup>17</sup>O excess (<sup>17</sup>Δ) and its simplicity compared to previous iterative calculation methods. Although he correctly points out that differences in the normalised gross production rate (<i>g</i>) are largely due to different input parameters used in Kaiser's "base case" and previous studies, he does not acknowledge Kaiser's observation that iterative and dual-delta calculation methods give exactly the same <i>g</i> for the same input parameters (disregarding kinetic isotope fractionation during air-sea exchange). The comment is based on misunderstandings with respect to the "base case" <sup>17</sup>δ<sub>P</sub> and <sup>18</sup>δ<sub>P</sub> values. Since direct measurements of <sup>17</sup>δ<sub>P</sub> and <sup>18</sup>δ<sub>P</sub>do not exist or have been lost, Kaiser constructed the "base case" in a way that was consistent and compatible with literature data. Nicholson showed that an alternative reconstruction of <sup>17</sup>δ<sub>P</sub> gives <i>g</i> values closer to previous studies. However, unlike Nicholson, we refrain from interpreting either reconstruction as a benchmark for the accuracy of <i>g</i>. A number of publications over the last 12 months have tried to establish which of these two reconstructions is more accurate. Nicholson draws on recently revised measurements of the relative <sup>17</sup>O/<sup>16</sup>O difference between VSMOW and Air-O<sub>2</sub> (<sup>17</sup>δ<sub>VSMOW</sub>; Barkan and Luz, 2011), together with new measurements of photosynthetic isotope fractionation, to support his comment. However, our own measurements disagree with these revised <sup>17</sup>δ<sub>VSMOW</sub> values. If scaled for differences in <sup>18</sup>δ<sub>VSMOW</sub>, they are actually in good agreement with the original data (Barkan and Luz, 2005) and support Kaiser's "base case" <i>g</i> values. The statement that Kaiser's <i>g</i> values are "30% too high" can therefore not be accepted, pending future work to reconcile different <sup>17</sup>δ<sub>VSMOW</sub> measurements. Nicholson also suggests that approximated calculations of gross production should be performed with a triple isotope excess defined as <sup>17</sup>Δ<sup>#</sup>≡ ln (1+<sup>17</sup>δ)–λ ln(1+<sup>18</sup>δ), with λ = θ<sub>R</sub> = ln(1+<sup>17</sup>ϵ<sub>R</sub> ) / ln(1+<sup>18</sup>ϵ<sub>R</sub>). However, this only improves the approximation for certain <sup>17</sup>δ<sub>P</sub> and <sup>18</sup>δ<sub>P</sub> values, for certain net to gross production ratios (<i>f</i>) and for certain ratios of gross production to gross Air-O<sub>2</sub> invasion (<i>g</i>). In other cases, the approximated calculation based on <sup>17</sup>Δ<sup>†</sup> ≡<sup>17</sup>δ – κ <sup>18</sup>δ with κ = γ<sub>R</sub> = <sup>17</sup>ϵ<sub>R</sub>/<sup>18</sup>ϵ<sub>R</sub> (Kaiser, 2011a) gives more accurate results.http://www.biogeosciences.net/9/2921/2012/bg-9-2921-2012.pdf
spellingShingle J. Kaiser
O. Abe
Reply to Nicholson's comment on "Consistent calculation of aquatic gross production from oxygen triple isotope measurements" by Kaiser (2011)
Biogeosciences
title Reply to Nicholson's comment on "Consistent calculation of aquatic gross production from oxygen triple isotope measurements" by Kaiser (2011)
title_full Reply to Nicholson's comment on "Consistent calculation of aquatic gross production from oxygen triple isotope measurements" by Kaiser (2011)
title_fullStr Reply to Nicholson's comment on "Consistent calculation of aquatic gross production from oxygen triple isotope measurements" by Kaiser (2011)
title_full_unstemmed Reply to Nicholson's comment on "Consistent calculation of aquatic gross production from oxygen triple isotope measurements" by Kaiser (2011)
title_short Reply to Nicholson's comment on "Consistent calculation of aquatic gross production from oxygen triple isotope measurements" by Kaiser (2011)
title_sort reply to nicholson s comment on consistent calculation of aquatic gross production from oxygen triple isotope measurements by kaiser 2011
url http://www.biogeosciences.net/9/2921/2012/bg-9-2921-2012.pdf
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