TY - JOUR
T1 - Coupled nitrate N and O stable isotope fractionation by a natural marine plankton consortium
AU - Rohde, Melissa M.
AU - Granger, Julie
AU - Sigman, Daniel M.
AU - Lehmann, Moritz F.
N1 - Funding Information:
We thank Philippe Tortell (University of British Columbia), Barbara Seth (University of Basel), Julien Foriel (Princeton University) for laboratory support, and Chris Payne (University of British Columbia) and Evgeny Pakhomov (University of British Columbia) for support in the field. Comments by two reviewers helped improve the manuscript. This work was financially supported by the US NSF through grant OCE-0447570 to DS and the Center for Environmental BioInorganic Chemistry (CEBIC) Undergraduate Research Fellowship at Princeton University, and by SNF (Swiss National Science Foundation) R'Equip funds granted to ML.
Publisher Copyright:
© 2015 Rohde, Granger, Sigman and Lehmann.
PY - 2015
Y1 - 2015
N2 - The stable nitrogen (N) and oxygen (O) isotope ratios (15N/14N and 18O/16O, respectively) of nitrate (NO3-) were measured during incubations of freshly collected seawater to investigate the effect of light intensity on the isotope fractionation associated with nitrate assimilation and possible co-occurring regeneration and nitrification by in situ plankton communities. Surface seawater was collected off the coast of Vancouver, Canada in late fall and in late summer and was incubated under different laboratory light conditions for 10 and 30 days, respectively. In the late summer experiments, parallel incubations were supplemented with 15NH4+ and H218O tracers to monitor co-occurring nitrification. Differences in irradiance in the fall incubations resulted in slightly reduced nitrate consumption at low light but had no distinguishable impact on the N isotope effect (15ε) associated with NO3- assimilation, which ranged between 5 and 8‰. The late-summer community incubations, in contrast, showed significantly reduced growth rates at low light and more elevated 15ε of 11.9 ± 0.4‰, compared to 8.4 ± 0.3‰ at high-light conditions. The seasonal differences could reflect physiological adaptations of the fall plankton community to reduced irradiance, such that their incubation at low light did not elicit the increase in proportional cellular nitrate efflux required to raise the isotope effect. In both the fall and summer incubations, the ratio of the coincident rises in the δ15N and δ18O of NO3- was comparable to previous monoculture phytoplankton experiments, with a Δδ18O:Δδ15N of ~1, regardless of light level. A decoupling of Δδ18O:Δδ15N is expected if nitrification occurs concomitantly with nitrate assimilation. The lack of such decoupling is best explained by the absence of significant nitrification in any of our study's treatments, an interpretation supported by our inability to identify any tracer 15N and 18O uptake into the NO3- pool in the late-summer community incubations.
AB - The stable nitrogen (N) and oxygen (O) isotope ratios (15N/14N and 18O/16O, respectively) of nitrate (NO3-) were measured during incubations of freshly collected seawater to investigate the effect of light intensity on the isotope fractionation associated with nitrate assimilation and possible co-occurring regeneration and nitrification by in situ plankton communities. Surface seawater was collected off the coast of Vancouver, Canada in late fall and in late summer and was incubated under different laboratory light conditions for 10 and 30 days, respectively. In the late summer experiments, parallel incubations were supplemented with 15NH4+ and H218O tracers to monitor co-occurring nitrification. Differences in irradiance in the fall incubations resulted in slightly reduced nitrate consumption at low light but had no distinguishable impact on the N isotope effect (15ε) associated with NO3- assimilation, which ranged between 5 and 8‰. The late-summer community incubations, in contrast, showed significantly reduced growth rates at low light and more elevated 15ε of 11.9 ± 0.4‰, compared to 8.4 ± 0.3‰ at high-light conditions. The seasonal differences could reflect physiological adaptations of the fall plankton community to reduced irradiance, such that their incubation at low light did not elicit the increase in proportional cellular nitrate efflux required to raise the isotope effect. In both the fall and summer incubations, the ratio of the coincident rises in the δ15N and δ18O of NO3- was comparable to previous monoculture phytoplankton experiments, with a Δδ18O:Δδ15N of ~1, regardless of light level. A decoupling of Δδ18O:Δδ15N is expected if nitrification occurs concomitantly with nitrate assimilation. The lack of such decoupling is best explained by the absence of significant nitrification in any of our study's treatments, an interpretation supported by our inability to identify any tracer 15N and 18O uptake into the NO3- pool in the late-summer community incubations.
KW - Marine ecology
KW - Nitrate assimilation
KW - Nitrate isotopes
KW - Nitrification
KW - Phytoplankton
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U2 - 10.3389/fmars.2015.00028
DO - 10.3389/fmars.2015.00028
M3 - Article
AN - SCOPUS:85008702203
SN - 2296-7745
VL - 2
JO - Frontiers in Marine Science
JF - Frontiers in Marine Science
IS - MAY
M1 - 28
ER -