Published July 2018 | Version v1
Journal article

Terrestrial dissolved organic matter distribution in the North Sea

  • 1. National Oceanography Centre, Southampton (United Kingdom)
  • 2. British Geological Survey, Wallingford (United Kingdom)
  • 3. Plymouth Marine Laboratory, Plymouth (United Kingdom)
  • 4. Centre for Environment, Fisheries and Aquaculture Science, Lowestoft (United Kingdom)
  • 5. Centre for Ecology and Hydrology, Environment Centre Wales, Bangor (United Kingdom)

Description

Highlights: • North Sea fluorescent DOM field sampled to map terrestrial inputs and distributions. • DOM pool characterised via absorbance and excitation-emission fluorescent spectra. • Three distinct FDOM fluorophores identified. • No clear evidence found for significant terrestrial DOM export to the Atlantic Ocean. • North Sea terrestrial DOM distributions appear stable over multi-decadal timescales. The flow of terrestrial carbon to rivers and inland waters is a major term in the global carbon cycle. The organic fraction of this flux may be buried, remineralized or ultimately stored in the deep ocean. The latter can only occur if terrestrial organic carbon can pass through the coastal and estuarine filter, a process of unknown efficiency. Here, data are presented on the spatial distribution of terrestrial fluorescent and chromophoric dissolved organic matter (FDOM and CDOM, respectively) throughout the North Sea, which receives organic matter from multiple distinct sources. We use FDOM and CDOM as proxies for terrestrial dissolved organic matter (tDOM) to test the hypothesis that tDOM is quantitatively transferred through the North Sea to the open North Atlantic Ocean. Excitation emission matrix fluorescence and parallel factor analysis (EEM-PARAFAC) revealed a single terrestrial humic-like class of compounds whose distribution was restricted to the coastal margins and, via an inverse salinity relationship, to major riverine inputs. Two distinct sources of fluorescent humic-like material were observed associated with the combined outflows of the Rhine, Weser and Elbe rivers in the south-eastern North Sea and the Baltic Sea outflow to the eastern central North Sea. The flux of tDOM from the North Sea to the Atlantic Ocean appears insignificant, although tDOM export may occur through Norwegian coastal waters unsampled in our study. Our analysis suggests that the bulk of tDOM exported from the Northwest European and Scandinavian landmasses is buried or remineralized internally, with potential losses to the atmosphere. This interpretation implies that the residence time in estuarine and coastal systems exerts an important control over the fate of tDOM and needs to be considered when evaluating the role of terrestrial carbon losses in the global carbon cycle.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.scitotenv.2018.02.237

Additional details

Identifiers

DOI
10.1016/j.scitotenv.2018.02.237;
PII
S0048969718306363;

Publishing Information

Journal Title
Science of the Total Environment
Journal Volume
630
Journal Page Range
p. 630-647
ISSN
0048-9697
CODEN
STENDL

INIS

Country of Publication
Netherlands
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
53029123
Subject category
S54: ENVIRONMENTAL SCIENCES;
Descriptors DEI
BALTIC SEA; BIOGEOCHEMISTRY; CARBON CYCLE; COASTAL WATERS; FILTERS; FLUORESCENCE; NORTH SEA; ORGANIC MATTER; RHINE RIVER; SALINITY; SPATIAL DISTRIBUTION
Descriptors DEC
ATLANTIC OCEAN; CHEMISTRY; DISTRIBUTION; EMISSION; GEOCHEMISTRY; LUMINESCENCE; MATTER; PHOTON EMISSION; RIVERS; SEAS; SURFACE WATERS

Optional Information

Copyright
Copyright (c) 2018 The Author(s). Published by Elsevier B.V.