Discerning the concentration and bi-directional flux of ammonia in an
urban estuary using the relaxed eddy accumulation method
Abstract
Narragansett Bay, the largest estuary in the northeastern U.S., is a
heavily urbanized watershed impacted by deposition and runoff. Nutrient
budgets and local policy rely on deposition data from a 1990 study that
did not include any direct observations of dry deposition of gaseous
ammonia (NH3) and particulate ammonium (NH4+) due to uncertainties in
their flux direction and measurement difficulty. Recent precipitation
measurements show that wet deposition of NH4+ to the Bay has increased
by a factor of 6 over the past three decades, leading to a 2.5-fold
increase in wet nitrogen (N) deposition. The documented increase in wet
deposition of NH4+ concurrent with managed nutrient reductions in
urbanized estuaries has potentially increased the impacts of atmospheric
N deposition, including the dry deposition of NH3 and NH4+. However, a
scarcity of measurements hinders our interpretation of this important N
source. For the first time over Narragansett Bay, and to our knowledge
over open water, dry (particulate and gas phase) deposition of total NHx
(NHx = NH3 + NH4+) and bidirectional NH3 flux was quantified using a
relaxed eddy accumulation sampling technique. We find that total N
entering the Bay from the atmosphere has doubled since 1990. Dry
deposition of NHx comprises 9.6% of total N deposition. During the fall
season, the dominant flux direction for NH3 is upward, which also has
implications for urban air quality. We estimate that NH3 emitted from
the Bay to the atmosphere makes up to 10% of the local NH3 emission
budget.