Table of Contents

• Dataset Description
  • Methods & Sampling
• Data Files
• Parameters
• Instruments
• Deployments
• Project Information
• Program Information
• Funding

Nitrogen-15 uptake rates for labeled substrates of NO2, NO3, NH4 and UREA

   PI:              James McCarthy and John Nevins
   of:              Harvard University
   dataset:         Nitrogen-15 uptake rates for labeled substrates of NO2,
                    NO3, NH4 and UREA
   dates:           May 18, 1989 to June 06, 1989
   location:
   project/cruise:  North Atlantic Bloom Experiment/Atlantis II 119,  leg 5
   ship:            R/V Atlantis II

Methodology:

Summary of methods used to determine new production and N cycling by N incorporation by phytoplankton, and euphotic zone NH+ concentrations using a high sensitivity assay during cruise #119 of the R/V Atlantis II: A component of the U.S. JGOFS North Atlantic Bloom Experiment (NABE)

James J. McCarthy and John L. Nevins

N Uptake Experiments

Water from 6 depths in the euphotic zone distributed from 60 - 0.1% Io was obtained from routine "productivity" casts conducted by the Scripps PACODF group deploying a rosette sampler equiped with 30 l Niskin bottles fitted with teflon coated springs. Water for the N experiments was transfered from the Niskin bottles to darkened 20 l polypropylene carboys, transported to a laboratory, and dispensed into 3 l polycarbonate incubation bottles. Three incubation bottles were prepared from each sample depth, and spiked with N-labeled (>98 At%) NH+, NO-, or NO- (or alternately urea) to ~10% of the ambient concentration, or not less than 10 nM. Ambient nutrient concentrations were provided by C. Garside who deployed a pump profiling system coupled to an auto analyzer in an operation prior to each productivity cast.

Immediately after labeling the samples, they were transfered to deck-board incubator tanks supplied with flowing sea-surface water providing mixed-layer temperature conditions, and screened with neutral density material to simulate the in situ light level. The experiments were incubated for 3-4 hrs and terminated by filtration through Whatman 47 mm GF/F glass fiber filters (precombusted at 450° C for 1 hr) and rinsed with 50 ml of GF/F filtered sea water. The filters were placed into individual polyethylene envelopes, dried at 60° in a gravity drying oven, and stored in an air tight container with silica gel desiccant. On selected samples in each profile, 500 ml of the filtrate was retained for NH+ and NO- extraction and subsequent isotopic analysis in order to determine the degree of isotope dilution which occurred during the course of the experiments. The method of Brzezinski (1987) incorporating solid phase extraction proceedures (J.T. Baker, 3 ml, C18 cartridges) was used to extract NH+. In the case of NO-, reagents were added to the filtrate to form an analine compound (Horrigan et al. 1990) which was then extracted using the solid phase techniques employed for NH+. If necessary, prior to extraction, unenriched carrier NO- or NH+ was added to these samples to bring their mass to ~40µg of N for isotopic analysis. The final eluate was collected and stored in sealed 3 ml, combusted, Pyrex glass vials (1 hr @ 450° C). In the laboratory, shortly before isotopic analysis, the eluate was reduced to a volume of ~0.5 ml by evaporation on a hot plate at ~80° C, and transfered by pipette to a combusted Whatman 25 mm GF/F glass fiber filter and dried in a gravity oven at 60° C. With the the isotopic data obtained from the NO- and NH+ extraction samples, uptake rates corrected for isotope dilution and NH+ remineralization and 1° nitrification rates were calculated (Horrigan et al. 1990).

N enrichment of the samples was determined by mass spectrometry in our laboratory at Harvard University, using methods and instrumentation described previously (Nevins and McCarthy 1982). Particulate N from each sample was obtained manometrically from the mass spectrometer sample preparation system and these data were used in the subsequent rate calculations. NH+ uptake rates were calculated using concentration data obtained from the nM method of Brzezinski (1987), used with solid phase extraction (J.T. Baker, 3 ml, C18 cartridges). Other uptake rates were calculated using data from the ship-board auto analyzer system (C.Garside) obtained from discrete samples from the Niskin bottles.

Because of the strong diel pattern observed in NO- uptake through out the period of observations, it would be inappropriate to use the discrete rates directly in estimates of new production (eg. an f ratio). We are preparing a manuscript (McCarthy, Nevins and Garside) which will present the results of an analysis which uses these data to model NO- uptake on an integrated daily basis.

Literature Cited:

Brzezinski, M.A. 1987.

Colorimetric determination of nanomolar concentrations of ammonium in seawater using solvent extraction. Mar. Chem. 19: 322-330.

Horrigan, S.G., J.P. Montoya, J.L. Nevins, J.J. McCarthy, H.W. Ducklow, R. Goericke and T. Malone. 1990.

Nitrogenous nutrient transformations in the spring and fall in the Chesapeake Bay. Est. Coast. Shelf Sci. 30: 369-391.

Nevins, J.L. and J.J. McCarthy. 1982.

N tracer studies in marine ecosystems. Nuclide Spectra (Publ. 1041/1082 Nuclide Corp.) 17: 1-2.

One of the first major activities of JGOFS was a multinational pilot project, North Atlantic Bloom Experiment (NABE), carried out along longitude 20° West in 1989 through 1991. The United States participated in 1989 only, with the April deployment of two sediment trap arrays at 48° and 34° North. Three process-oriented cruises where conducted, April through July 1989, from R/V Atlantis II and R/V Endeavor focusing on sites at 46° and 59° North. Coordination of the NABE process-study cruises was supported by NSF-OCE award # 8814229. Ancillary sea surface mapping and AXBT profiling data were collected from NASA's P3 aircraft for a series of one day flights, April through June 1989.

A detailed description of NABE and the initial synthesis of the complete program data collection efforts appear in: Topical Studies in Oceanography, JGOFS: The North Atlantic Bloom Experiment (1993), Deep-Sea Research II, Volume 40 No. 1/2.

The U.S. JGOFS Data management office compiled a preliminary NABE data report of U.S. activities: Slagle, R. and G. Heimerdinger, 1991. U.S. Joint Global Ocean Flux Study, North Atlantic Bloom Experiment, Process Study Data Report P-1, April-July 1989. NODC/U.S. JGOFS Data Management Office, Woods Hole Oceanographic Institution, 315 pp. (out of print).

The United States Joint Global Ocean Flux Study was a national component of international JGOFS and an integral part of global climate change research.

The U.S. launched the Joint Global Ocean Flux Study (JGOFS) in the late 1980s to study the ocean carbon cycle. An ambitious goal was set to understand the controls on the concentrations and fluxes of carbon and associated nutrients in the ocean. A new field of ocean biogeochemistry emerged with an emphasis on quality measurements of carbon system parameters and interdisciplinary field studies of the biological, chemical and physical process which control the ocean carbon cycle. As we studied ocean biogeochemistry, we learned that our simple views of carbon uptake and transport were severely limited, and a new "wave" of ocean science was born. U.S. JGOFS has been supported primarily by the U.S. National Science Foundation in collaboration with the National Oceanic and Atmospheric Administration, the National Aeronautics and Space Administration, the Department of Energy and the Office of Naval Research. U.S. JGOFS, ended in 2005 with the conclusion of the Synthesis and Modeling Project (SMP).