The fractionation of nitrogen and oxygen isotopes in macroalgae during the assimilation of nitrate

In order to determine and understand the stable isotope fractionation of <sup>18</sup>O and <sup>15</sup>N manifested during assimilation of NO<sub>3</sub><sup>&minus;</sup> in marine macro-benthic algae, two species (<i>Ulva</i> sp. an...

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Bibliographic Details
Main Authors: P. K. Swart, S. Evans, T. Capo, M. A. Altabet
Format: Article
Language:English
Published: Copernicus Publications 2014-11-01
Series:Biogeosciences
Online Access:http://www.biogeosciences.net/11/6147/2014/bg-11-6147-2014.pdf
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Summary:In order to determine and understand the stable isotope fractionation of <sup>18</sup>O and <sup>15</sup>N manifested during assimilation of NO<sub>3</sub><sup>&minus;</sup> in marine macro-benthic algae, two species (<i>Ulva</i> sp. and <i>Agardhiella</i> sp.) have been grown in a wide range of NO<sub>3</sub><sup>&minus;</sup> concentrations (2–500 μM). Two types of experiments were performed. The first was one in which the concentration of the NO<sub>3</sub><sup>&minus;</sup> was allowed to drift downward as it was assimilated by the algae, between 24 hour replacements of media. These experiments proceeded for periods of between 7 and 10 days. A second set of experiments maintained the NO<sub>3</sub><sup>&minus;</sup> concentration at a low steady-state value by means of a syringe pump. The effective fractionation during the assimilation of the NO<sub>3</sub><sup>&minus;</sup> was determined by measuring the δ<sup>15</sup>N of both the (i) new algal growth and (ii) residual NO<sub>3</sub><sup>&minus;</sup> in the free-drift experiments after 0, 12, 24 and 48 h. Modelling these data show that the fractionation during assimilation is dependent upon the concentration of NO<sub>3</sub><sup>&minus;</sup> and is effectively 0 at concentrations of less than ~2 μM. The change in the fractionation with respect to concentration is the greatest at lower concentrations (2–10 μM). The fractionation stablizes between 4 and 6&permil; at concentrations of between 50 and 500 μM. Although the δ<sup>18</sup>O and δ<sup>15</sup>N values of NO<sub>3</sub><sup>&minus;</sup> in the residual solution were correlated, the slope of relationship also varied with respect to NO<sub>3</sub><sup>&minus;</sup> concentration, with slopes of greater than unity at low concentration. These results suggest shifts in the dominant fractionation mechanism of <sup>15</sup>N and <sup>18</sup>O between concentrations of 1 and 10 μM NO<sub>3</sub><sup>&minus;</sup>. At higher NO<sub>3</sub><sup>&minus;</sup> concentrations (>10–50 μM), fractionation during assimilation will lead to δ<sup>15</sup>N values in algal biomass lower than the ambient NO<sub>3</sub><sup>&minus;</sup> and <sup>15</sup>N enrichments in the residual NO<sub>3</sub><sup>&minus;</sup>.
ISSN:1726-4170
1726-4189