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(15N-ρNH4+) uptake Regenerated Production

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Revision as of 10:45, 12 May 2026 by Hagi BucknWise (talk | contribs) (Created page with "{{BreadcrumbsNutrients}} * Page authors: PRIMO * Responsible curator: Hagen Buck-Wiese ---- __TOC__ <div class="model-box"> {| class="model-ib" style="float:right; margin-left:1em; margin-bottom:1em;" ! Ammonium uptake (regenerated production) |- | '''Approach:''' <sup>15</sup>N tracer incubation, EA-IRMS |- | '''Context:''' incubation, simulated ''in situ'' |- | '''Spatial scale:''' point sample |-...")
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Ammonium uptake (regenerated production)
Approach: 15N tracer incubation, EA-IRMS
Context: incubation, simulated in situ
Spatial scale: point sample
Temporal scale: 12–24 h
Units: µmol N L-1 d-1; µmol N m-2 d-1 (depth-integrated)
Community captured: all (usually > 0.2 µm)
Co-measurements: background δ15N (PON), ambient [NH4+], temperature, PAR, Chl, initial blank; dark uptake; can couple with 13C uptake

Method Overview

15N-labelled ammonium (15NH4Cl) is added to seawater samples at tracer concentrations and incubated under simulated in situ conditions. In the framework of Eppley & Peterson (1979), ammonium-based nitrogen uptake corresponds to regenerated production — the recycling of previously fixed nitrogen within the euphotic zone[1]. After incubation, the particulate fraction is collected on GFF filters; 15N enrichment in PN is measured by EA-IRMS, and the absolute uptake rate (ρNH4+) is calculated using the constant-flux model[2].

Scale of measurement

Point sample; 12–24 h incubation integrating over a diel cycle.

Data generated

Ammonium uptake rates in µmol N L-1 d-1. Combined with nitrate and urea uptake, the f-ratio and the relative contributions of different nitrogen sources to total nitrogen nutrition are calculated.

Units & currency

Units are µmol N L-1 d-1. The currency is nitrogen.

Sample size

Typical samples are 0.5–2 L in volume.

Repositories & databases

Limitations

A critical limitation is that ambient [NH4+] in the euphotic zone is often very low (nM range), which can violate the tracer requirement: adding sufficient 15NH4+ to achieve measurable enrichment may perturb the system. Additionally, ongoing microbial regeneration of NH4+ from unlabelled organic matter during the incubation dilutes the 15N pool, causing underestimation of true uptake rates (isotope dilution). Bottle effects apply.

Example Applications & Protocols

Classic examples

  • Dugdale & Goering (1967) Uptake of new and regenerated forms of nitrogen in primary productivity [3]
  • Dugdale & Wilkerson (1986) The use of 15N to measure nitrogen uptake in eutrophic oceans [2]

Recent applications

  • Varela et al. (2013) Pelagic primary productivity and upper ocean nutrient dynamics across subarctic and Arctic seas [4]

Common calculations/conversions

  • ρNH4+ is calculated identically to ρNO3-; the isotope dilution correction of Glibert et al. should be applied when regeneration is significant.

References

  1. Eppley, R. W., & Peterson, B. J. (1979). Particulate organic matter flux and planktonic new production in the deep ocean. Nature, 282, 677–680. https://doi.org/10.1038/282677a0
  2. 2.0 2.1 Dugdale, R. C., & Wilkerson, F. P. (1986). The use of 15N to measure nitrogen uptake in eutrophic oceans; experimental considerations. Limnology and Oceanography, 31(4), 673–689. https://doi.org/10.4319/lo.1986.31.4.0673
  3. Dugdale, R. C., & Goering, J. J. (1967). Uptake of new and regenerated forms of nitrogen in primary productivity. Limnology and Oceanography, 12(2), 196–206. https://doi.org/10.4319/lo.1967.12.2.0196
  4. Varela, D. E., Crawford, D. W., Wrohan, I. A., Wyatt, S. N., & Carmack, E. C. (2013). Pelagic primary productivity and upper ocean nutrient dynamics across subarctic and Arctic seas. Journal of Geophysical Research: Oceans, 118, 7132–7152. https://doi.org/10.1002/2013JC009211