Nitrogen and carbon cycling in the South Atlantic Ocean: a stable isotope study along a 40°S transect (UK GEOTRACES)
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Date
30/06/2015Author
Tuerena, Robyn Elizabeth
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Abstract
Fixed N (nitrate, nitrite, and ammonium) is a limiting nutrient for photosynthesis in
the surface ocean. The rates and relative importance of N cycling processes,
however, are temporally and spatially complex, which hamper their direct
measurement and quantification. The South Atlantic subtropical front separates the
Atlantic Ocean and the subantarctic, an area which can elucidate information about
water masses both entering and leaving the basin. Through the GEOTRACES
programme, an oceanographic section across 40°S in the South Atlantic is used to
investigate biogeochemical cycling of nitrogen and carbon in this region.
Hydrographic data, in combination with the isotopic composition of nitrate (NO3-),
particulate organic carbon and particulate nitrogen (δ15NNO3, δ18ONO3, δ13CPOC,
δ15NPN), is used to provide integrative measurements for temporally and spatially
variable processes of the marine N-cycle and C-cycle.
A thorough examination of the stable isotope cycling of particulate and dissolved N
across the subtropical front is used to quantify the supply of fixed N to the mixed
layer. The relative importance of nitrate from the subsurface, N2 fixation, terrestrial
input and atmospheric deposition in supplying production is determined. Typically,
30-50% of the export flux in the subtropical water masses is sourced from N2 fixers
and up to 75% within the Brazil Current. This finding suggests that diazotrophs may
be abundant in the South West Atlantic providing a source of new N to this region.
To assess the basin scale N-cycling processes, the deep water masses were analysed
to reveal the origin and history of NO3-. Intermediate waters formed in the
subantarctic are enriched in δ15NNO3 and δ18ONO3 from partial utilisation by algae.
This enrichment in δ15NNO3 is not present in the subtropical North Atlantic or the
return flow of the North Atlantic Deep Water (NADW), which decreases from
~5.9‰ in the newly formed intermediate waters to ~4.8‰ in the NADW at 40°S.
The modification of isotopic signatures through the subtropical Atlantic can be
calculated as an incorporation of 26-36 Tg N yr-1 of newly fixed N from an isotopic
source of -1‰ (N2 fixation). The extent of N addition is higher than estimated rates
of N loss within the Atlantic and surpasses the amount of N deficit supplied to the
basin.
Fixed N inputs and losses through the global ocean are investigated by the
assessment of remineralised nitrate added to the ocean interior. A lower δ15N is
observed in Atlantic remineralised nitrate in comparison to the Pacific. The relative
importance of N2 fixation and pelagic denitrification within each ocean basin is
quantified and through this approach, N2 fixation rates are estimated at 92-116 Tg N
yr-1 in the Pacific and 24-32 Tg N yr-1 in the Indian Ocean. Combining Atlantic N2
fixation of ~32 Tg N yr-1 with Indo-Pacific, global N2 fixation rates can be estimated
at 142-184 Tg N yr-1. The high inputs in the Pacific suggest that excess P is the
dominant control on the success of N2 fixers. However, estimates of new N addition
to the Atlantic indicate other mechanisms such as the recycling efficiency of P and
supply of Fe to the surface ocean increase N2 fixation rates above this threshold.
The organic matter supplied to sediments is principally derived from phytoplankton
across the subtropical front. High organic content is associated with the productive
Brazil-Malvinas Confluence region where a diverse supply of nutrients sustains
elevated biomass. The Rio Plata outflow is characterised with high δ15NNO3 and
δ15NPN, suggesting denitrification processes occur in the estuary. A low δ13C source
associated with high Al concentrations is identified on the western slope, indicating a
supply of terrestrial derived C to the deep ocean. The fractionation of C uptake by
phytoplankton is assessed in subtropical and subantarctic waters. In the subantarctic,
CO2[aq] and growth rates determine the extent of C isotope fractionation. In this
region, low species diversity and a small range in cell size enable the fractionation
from CO2[aq] and growth rate to be expressed in phytoplankton. In subtropical water
masses a larger range of cell size is the principal determinant of C fractionation.
Increased surface area to volume is the main mechanism for increasing C uptake,
arguing against the use of δ13CPOC as a palaeoproxy. The low δ13CPOC and δ15NPN
observed in the subtropics (from C fractionation and N2 fixation) contrast the heavier
signatures in the subantarctic. These observations are propagated to the sediments,
wherein organic matter shifts are determined by changes in the subtropical front over
time. The results of this study have greatly improved knowledge of N and C cycling
within the South Atlantic, providing new insight into the cycling of these two
important elements in the surface and deep ocean, on a regional and global scale.