2019•ACS Earth and Space ChemistryRequires access

What Fractionates Oxygen Isotopes during Respiration? Insights from Multiple Isotopologue Measurements and Theory

Jeanine L. Ash, Huanting Hu, Laurence Y. Yeung

Open publisher page 30 citations

Abstract

The precise mass dependence of respiratory O 2 consumption underpins the “oxygen triple-isotope” approach to quantifying gross primary productivity in modern and ancient environments. Yet, the physical-chemical origins of the key 18 O/ 16 O and 17 O/ 16 O covariations observed during respiration have not been tied to theory; thus, the approach remains empirical. First-principles calculations on enzyme active-site models suggest that changes in the O–O bond strength upon electron transfer strongly influence respiratory isotopic fractionation. However, molecular diffusion may also be important. Here, we use measurements of the relative abundances of rare isotopologues 17 O 18 O and 18 O 18 O as additional tracers of mass dependence during dark respiration experiments of lacustrine water. We then compare the experimental results to first-principles calculations of O 2 interacting with heme-oxidase analogues. We find a significantly steeper mass dependence, supported by theory, than has been previously observed. Enrichments of 17 O 18 O and 18 O 18 O in the O 2 residue suggest that θ values are strongly influenced by chemical processes, rather than being dominated by physical processes (i.e., by bond alteration rather than diffusion). In contrast, earlier data are inconsistent with theory, implying that analytical artifacts may have biased those results. Implications for quantifying primary productivity are discussed.

About this research paper

What this paper is about

The precise mass dependence of respiratory O 2 consumption underpins the “oxygen triple-isotope” approach to quantifying gross primary productivity in modern and ancient environments. Yet, the physical-chemical origins of the key 18 O/ 16 O and 17 O/ 16 O covariations observed during respiration have not been tied to theory; thus, the approach remains empirical. First-principles calculations on enzyme active-site models suggest that changes in the O–O bond strength upon electron transfer strongly influence respiratory isotopic fractionation. However, molecular diffusion may also be important. Here, we use measurements of the relative abundances of rare isotopologues 17 O 18 O and 18 O 18 O as additional tracers of mass dependence during dark respiration experiments of lacustrine water. We then compare the experimental results to first-principles calculations of O 2 interacting with heme-oxidase analogues. We find a significantly steeper mass dependence, supported by theory, than has been previously observed. Enrichments of 17 O 18 O and 18 O 18 O in the O 2 residue suggest that θ values are strongly influenced by chemical processes, rather than being dominated by physical processes (i.e., by bond alteration rather than diffusion). In contrast, earlier data are inconsistent with theory, implying that analytical artifacts may have biased those results. Implications for quantifying primary productivity are discussed.

Why it matters

OpenAlex reports 30 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

The precise mass dependence of respiratory O 2 consumption underpins the “oxygen triple-isotope” approach to quantifying gross primary productivity in modern and ancient environments. Yet, the physical-chemical origins of the key 18 O/ 16 O and 17 O/ 16 O covariations observed during respiration have not been tied to theory; thus, the approach remains empirical. First-principles calculations on enzyme active-site models suggest that changes in the O–O bond strength upon electron transfer strongly influence respiratory isotopic fractionation. However, molecular diffusion may also be important. Here, we use measurements of the relative abundances of rare isotopologues 17 O 18 O and 18 O 18 O as additional tracers of mass dependence during dark respiration experiments of lacustrine water. We then compare the experimental results to first-principles calculations of O 2 interacting with heme-oxidase analogues. We find a significantly steeper mass dependence, supported by theory, than has been previously observed. Enrichments of 17 O 18 O and 18 O 18 O in the O 2 residue suggest that θ values are strongly influenced by chemical processes, rather than being dominated by physical processes (i.e., by bond alteration rather than diffusion). In contrast, earlier data are inconsistent with theory, implying that analytical artifacts may have biased those results. Implications for quantifying primary productivity are discussed.

Key concepts: Isotopologue, Mass-independent fractionation, Chemistry, Respiration, Kinetic isotope effect, Oxygen, Isotope, Diffusion

Related papers

Back to paper searchBrowse research topicsOriginal source
What Fractionates Oxygen Isotopes during Respiration? Insights from Multiple Isotopologue Measurements and Theory — Research Paper | ScholarLens