2528
F. Große et al.: Looking beyond stratification
Biogeosciences, 13, 2511-2535, 2016
www.biogeosciences.net/13/2511/2016/
Region no. 04:20 02
— Oxygen cone.
■ 1 Oxygen sat.
Vert, mixing
Advection
" ■ Primary prod.
Zoopl. respir.
Pelagic remln.
Benthic remin.
Nitrification
I strat. period:
28/03-06/09
thickness:
bot. depth:
: area:
: voliume:
b.2p m
45.00 m
1.91g+09
1.19E+1Q
m 2
m 3
(a)
"O c? ^9 *0 V V
-70
lajeo
50
40
30
20
10
0
-10
-20
-30
-40
: strat. period:
30/03-26/10
thickness:
böt. depth:
area:
; voliume:
9.2b m
99.2Î3 m
1.77E+09
1.63ÎE+10
m 2
m 3
(b)
-20
-30
-40
'is 6- Up 'o
Figure 9. Mass balances of simulated bottom Ot in regions 4 (a) and 5 (b); (see Fig. 2) during stratification (grey shaded) in 2002. Same
legend for (a) and (b). Black y axes apply to processes, magenta y axes apply to Ot (saturation) concentrations. Changes in Ot due to
different processes are cumulative.
stratified period, but revealed a faster decrease in bottom O2
during 2007 compared to 2008. As the simulation showed the
same tendency with respect to the differences between the 2
years, the mass balances for station North Dogger for 2007
and 2008 are presented in Fig. 10a and b, respectively, in or
der to interpret the observed temporal evolution of bottom
O2.
The simulation yields an average rate of O2 reduction
during the stratified period of about 0.009 mg CFL -1 d -1 in
2007, and a rate of about 0.007 mg CL L _1 d _1 in 2008. The
integrated effect of the physical factors, ADVo, and MIXo,,
is quite similar for both years providing a gross increase in
O2 of about 16.3 g 02 m -2 integrated over the stratified pe
riod. Thus, the main variations between the 2 years must be
related to biological factors.
The temporal evolution of the biological consumption pro
cesses is also similar in both years, with higher rates in 2007.
The integrated effect of all biological sink processes results
in —40.6 g02 m -2 , which corresponds to an average con
sumption rate of 0.18 g O2 m -2 d _ 1 . For 2008, the simulation
yields a 6.8g02m -2 lower biological consumption due to
a 0.02 gCL m -2 d -1 lower consumption rate. This constitutes
a relative difference of 13 % between the 2 years. For EXP org
below 25 m depth during summer (calculation analogous to
Table 1), the same relative difference is found.
The relative contribution of the different processes to the
overall bottom CL consumption shows only minor changes
between the 2 years. In both years REM se d accounts for about
58 %, while REMpei accounts for about 31 %. RES zoo and
NIT contribute to about 3 and 8 % in both years, respec
tively. This shows that the variations in the CL dynamics
between 2007 and 2008 at North Dogger are mainly driven
by differences in the organic matter export. The steeper de
crease in bottom CL in 2007 results from the enhanced sup
ply of organic matter and the subsequent increased degra
dation by bacteria. The enhanced release of ammonium due
to pelagic and benthic remineralisation consequently triggers
an increase in nitrification.
In contrast to the findings by Greenwood et al. (2010), who
argued that the relatively strong advection at North Dogger
may ventilate the bottom layers in terms of CL, our results
suggest that advection only has a minor positive effect due to
the only slightly higher CL concentrations in the surround
ing waters. The large contribution of bacterial remineralisa
tion (REM S ed and REMpei) accounting for almost 90% of
the overall biological consumption at station North Dogger
confirms that the estimates for C remineralisation rates made
by Greenwood et al. (2010) provide reasonable results. How
ever, as NIT also accounts for about 8 % of the total biolog
ical O2 consumption, this process should be considered to
obtain more precise estimates for C remineralisation rates.
4 Conclusions and perspectives
The North Sea is one of the shelf regions regularly experi
encing seasonal O2 deficiency in the bottom water (Diaz and
Rosenberg, 2008; Emeis et al., 2015; Rabalais et al., 2010).
However, not all areas of the North Sea are similarly affected
by low O2 conditions (e.g., Queste et al., 2013) due to differ
ent characteristics with respect to stratification and O2 con
sumption. Observations and model results suggest that the
area between 54-57° N and 4.5-7° E shows the highest po
tential for low O2 conditions, but also areas around the Dog-
gerbank experience lowered bottom O2 concentrations.