Dataset: Net primary production and nutrient data from R/V Hugh R. Sharp cruise HRS1414 CTD casts in the Mid and South-Atlantic Bight from July to August of 2014 (DANCE project)

ValidatedFinal no updates expectedDOI: 10.1575/1912/bco-dmo.733711.1Version 1 (2018-04-19)Dataset Type:Cruise Results

Principal Investigator: Margaret Mulholland (Old Dominion University)

Co-Principal Investigator: Raymond Najjar (Pennsylvania State University)

Co-Principal Investigator: Peter N. Sedwick (Old Dominion University)

BCO-DMO Data Manager: Amber D. York (Woods Hole Oceanographic Institution)


Project: Collaborative Research: Impacts of atmospheric nitrogen deposition on the biogeochemistry of oligotrophic coastal waters (DANCE)


Abstract

Net primary production (NPP) and nutrient data were acquired from R/V Hugh R. Sharp cruise HRS1414 CTD casts in the Mid and South-Atlantic Bight from July to August of 2014 between latitudes 31.60°N and 38.89°N, and longitudes 71.09°W and 75.16°W.

Codes in the data:
* ND: not determined
* BDL: below detection limit
* DNP: Data not presented

Water column sample collection and in-situ measurements:

Water-column samples for analysis of Chl a, nitrate, nitrite, phosphate, urea, ammonium and net primary productivity, and continuous profiles of temperature and salinity were collected using a conductivity-temperature-depth sensor (SBE 911 plus) with a 12 Bottle Frame & Carousel (SBE 32) consisting of 12 niskin bottles. Nutrient samples were collected from the niskin bottles using acid cleaned tubing and were filtered through a 0.2 µm filter. Whole water samples to measure net primary production were collected directly from CTD bottles using acid cleaned tubing and drained into acid cleaned 10L carboys. Measurement of net primary production was done using stable isotopes. Whole water samples were taken with a niskin bottle from the surface, mix layer, and chlorophyll maximum and transferred into acid-cleaned 250 mL, 500mL, 1000ml or 2000ml PETG incubation bottles in triplicate. Primary productivity was measured by adding tracer additions (<10% of the ambient dissolved inorganic carbon) of NaH13CO2 and incubating for 12-24 hours in flow-through seawater incubators under neutral density screening. Dark bottles were also incubated. After 12-24 hours, incubations were terminated by filtration through pre-combusted (450 degree C for 2 h) GF/F filters. Filters were stored at -20 degree C until analysis in the laboratory. Filters were analyzed on a Europa 20/20 isotope ratio mass spectrometer equipped with an automated nitrogen and carbon analysis for gas, solids, and liquids (ANCA-GSL) preparation module. Analysis also resulted in particulate nitrogen (PN) and particulate carbon (PC) values.

NO3 & NO2: Dissolved nitrate and nitrite was determined at sea using an Astoria Pacific nutrient autoanalyzer using standard colorimetric methods with a detection limit of 0.14 µM (Parsons et al., 1984; Price and Harrison, 1987). In surface waters, nitrate and nitrite were determined using the same autoanalyzer equipped with a liquid waveguide capillary cell (World Precision Instruments) (Zhang, 2000) to achieve a detection limit of 0.02 µM.

PO4: Dissolved phosphate was determined at sea using an Astoria Pacific nutrient autoanalyzer using standard colorimetric methods with a detection limit of 0.03 µM (Parsons et al., 1984; Price and Harrison, 1987).

NH4: Dissolved ammonium was determined at sea using the manual orthophthaldialdehyde method (Holmes et al., 1999).

Urea: Dissolved urea was determined at sea using an Astoria Pacific nutrient autoanalyzer using standard colorimetric methods with a detection limit of 0.08 µM (Parsons et al., 1984; Price and Harrison, 1987).

Temperature: In-situ temperature was measured using a conductivity-temperature-depth sensor (SBE 911 plus).

Salinity: Salinity was calculated from in-situ conductivity, as measured using a conductivity-temperature-depth (CTD) sensor (SBE 911 plus).

Chl: Chlorophyll a was determined at sea using the non-acidification method with a Turner 10-AU fluorometer (Welschmeyer et al., 1994).

NPP: Net primary production was measured using stable isotopes (Mulholland et al., 2006).

PNPC: Particulate nitrogen and carbon samples were collected by filtering whole water samples through pre-combusted (450 degree C for 2 h) GF/F filters. Filters were stored at -20 degree C until analysis in the laboratory. Filters were analyzed on a Europa 20/20 isotope ratio mass spectrometer equipped with an automated nitrogen and carbon analysis for gas, solids, and liquids (ANCA-GSL) preparation module.


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Methods

Holmes, R. M., Aminot, A., Kérouel, R., Hooker, B. A., & Peterson, B. J. (1999). A simple and precise method for measuring ammonium in marine and freshwater ecosystems. Canadian Journal of Fisheries and Aquatic Sciences, 56(10), 1801–1808. doi:10.1139/f99-128
Methods

Mulholland, M. R., Bernhardt, P. W., Heil, C. A., Bronk, D. A., & O’Neil, J. M. (2006). Nitrogen fixation and release of fixed nitrogen by Trichodesmium spp. in the Gulf of Mexico. Limnology and Oceanography, 51(4), 1762–1776. doi:10.4319/lo.2006.51.4.1762
Methods

Parsons, T. R., Y. Maita, and C. M. Lalli. "A Manual of Chemical and Biological Methods of Seawater Analysis", Pergamon Press (1984). ISBN: 9780080302874
Methods

Price, N. M., & Harrison, P. J. (1987). Comparison of methods for the analysis of dissolved urea in seawater. Marine Biology, 94(2), 307–317. doi:10.1007/bf00392945
Methods

Welschmeyer, N. A. (1994). Fluorometric analysis of chlorophyll a in the presence of chlorophyll b and pheopigments. Limnology and Oceanography, 39(8), 1985–1992. doi:10.4319/lo.1994.39.8.1985