Environmental Engineering Reference
In-Depth Information
Table 19.1 Initial conditions speci
ed for cGENIE in this study
Parameters
Description
Value
Units
Ω calcite, init
Calcite surface saturation state
2.5, 5 and 10
Dimensionless
pH init
Ocean surface pH
7.7 (
Ω calcite, init ¼
10)
Dimensionless
7.55 (
Ω calcite, init ¼
5)
7.4 (
Ω calcite, init ¼
2.5)
C
T 0
Global average ocean surface
temperature
21
Tmol yr - 1
F w, calcite
Weathering
flux of calcite
17
Tmol yr - 1
F w, silicate
Weathering
flux of silicate
10.5
13 C w
13 C of weathering calcite
δ
δ
3.6
13 C outgassing
13 CofCO 2 from volcanic
outgassing
δ
δ
3.6
13 C atm
13 C of atmosphere
δ
δ
5
13 C DIC
13 C of DIC in surface ocean
δ
δ
2.9
[Ca 2 þ ]
Ca 2 þ concentrations in the
ocean
mmol kg - 1
13
p CO 2init
Initial atmospheric p CO 2
2800
ppm
10 18
0.5
mol
mol kg - 1
[DIC] surf
Surface ocean DIC
concentration
6035 (
Ω calcite, init ¼
10)
μ
4230 (
Ω calcite, init ¼
5)
2970 (
Ω calcite, init ¼
2.5)
mol kg - 1
[DIC] deep
Deep ocean DIC
concentration
6304 (
Ω calcite, init ¼
10)
μ
Ω calcite, init ¼
4450 (
5)
3160 (
Ω calcite, init ¼
2.5)
end-Permian extinction (Cui et al ., 2013 ). With a desired global mean surface
saturation value (e.g.
gured to
determine the appropriate initial ocean alkalinity (Alk) and DIC value (the initial
conditions of the model are summarized in Table 19.1 ).
Ω
¼
10, 5 and 2.5), cGENIE can be con
calcite
19.2.3 Forcing the DIC with CO 2 addition
We used the carbonate C isotope record of the GSSP (Global Boundary Stratotype
Section and Point) in Meishan, South China (Shen et al ., 2011 ) to perform a loess
fit (Matlab ® smoothing function
loess
), where a span parameter of 8% was
speci
ed, lower than that used in Cui et al .( 2013 ), to capture a larger magnitude
of CIE ( Figure 19.1 ). We then forced the ocean-surface DIC
13
δ
C to conform to the
13
13
prescribed
δ
C DIC derived from the statistically treated
δ
C carb , using an offset of
0.6
meant to account for the difference between the DIC and sedimentary
CaCO 3
13
13
C values of added CO 2 such that they represent
several proposed sources, including plume-released CO 2 (
δ
C. We varied the
δ
-
9
and
-
12
), CO 2
-
from mixed sources ( - 15
and
20
), contact metamorphism of coal and
-
-
kerogen (
25
), CO 2 from oxidation of thermogenic methane (
40
) and
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