Environmental Engineering Reference
In-Depth Information
The mooring data indicate a transient, sluggish bottom water layer of up to 30
m thickness. This layer appears to be stable for months. The slower the merid-
ional current component, the longer the residence time on the shelf, the more this
layer becomes oxygen- and nitrate-depleted, and ultimately sulphidic. At coast-
parallel bottom current speeds of 2 and 4 cm s 1 , water is transported within
approximately 600 and 300 days, respectively, from the Angola-Benguela front
to 26 S. Hence, this period can be taken as an approximate residence time for
shelf bottom water reaching 26 S.
4. PATHWAYS, RATES, AND AMOUNT OF WATER
COLUMN RESPIRATION
4.1 Aerobic Water Column Respiration
Generally, oxygen concentrations decrease rapidly below the thermocline
on the shelf as a result of the aerobic respiration of sinking organic material.
Video observations from a remotely operated vehicle during RV METEOR
Expedition M57-3 in March 2003 suggest that particulate organic material in
the water column over the shelf consists mostly of aggregates [42]. We have
used a new approach to estimate the rate of oxygen consumption in the water
column by combining volume-specific oxygen consumption rates of diatom
aggregates with abundances and size spectra of aggregates determined by in-
situ video observation during a diatom bloom in the southern Benguela system
[20]. Size-dependent rates of diffusive oxygen uptake in diatom aggregates
have been determined by [30]. Diffusive oxygen uptake varied as a function of
aggregate size, and was described by the relationship Q tot , vol = 65.8(vol) 0.67 ,
where Q tot , vol is the total oxygen consumption (nmol agg 1 h 1 ) as a function
of aggregate volume (vol) [30]. The above equation can be recast as a function
of aggregate radius, which yields the expression
171 r 2.0
(1)
where Q tot , r has the unit nmol O 2 cm 3 h 1 . Extrapolation of the aggregate
radius-specific respiration rate to a respiration rate per volume seawater requires
that the aggregate size spectrum in the water column is known. We used the
empirical relationship reported in Kiørboe and co-workers [20] for a diatom
bloom in the southern Benguela. The aggregate size spectrum was described
by the power function
Q tot , r =
b 3 r b 4
n r
=
(2)
where n r represents the volume-normalized number of aggregates, the sub-
script r is the aggregate radius, b 3 is a particle concentration coefficient and
b 4 describes the slope of the spectrum [19]. The larger b 4 , the smaller are the
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