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Marine Biogeochemical and Ecosystem Modeling

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Title: Marine Biogeochemical and Ecosystem Modeling


1
Marine Biogeochemical and Ecosystem Modeling
  • Michael Schulz
  • MARUM -- Center for Marine Environmental Sciences
  • and
  • Faculty of Geosciences, University of Bremen

2
  • 915 - 945
  • 1. Introduction (Lecture)- The global carbon
    cycle, CO2 in seawater
  • - Biological pumps
  • - Reservoir or box models
  • 2. Modeling Marine Nutrient and Carbon Cycles
    (Box-Model Exercise)- Global oceanic
    phosphate distribution
  • - Nutrient productivity interactions
  • - Oceanic carbon budget and large-scale ocean
    circulation
  • 1045 - 1100 break

3
  • 1100 1230
  • 2. cont'd- Circulation-productivity feedback in
    the global ocean
  • 3. State-of-the-art Biogeochemical Models
    (Lecture)- 2D and 3D Models- Included tracers
    and processes
  • 4. Marine Ecosystem Models (Lecture)
  • - Why ecosystem models?
  • - Ecosystem models in paleoceanography

4
Course Material
  • www.geo.uni-bremen.de/geomod/
  • staff/mschulz/lehre/ECOLMAS_Modeling/
  • This presentation
  • Box-model exercises

5
Basic Literature
  • Najjar, R. G., Marine biogeochemistry. in Climate
    system modeling, edited by Trenberth, K. E., pp.
    241-280, Cambridge University Press, Cambridge,
    1992.
  • Rodhe, H., Modeling biogeochemical cycles. in
    Global biogeochemical cycles, edited by Butcher,
    S. S., R. J. Charlson, G. H. Orians and G. V.
    Wolfe, pp. 55-72, Academic Press, London, 1992.
  • Sarmiento, J. L., and N. Gruber, Ocean
    biogeochemical dynamics, pp. 503, Princeton
    University Press, Princeton, 2006.
  • Walker, J. C. G., Numerical adventures with
    geochemical cycles, 192 pp., Oxford University
    Press, New York, 1991.

6
For a climatologist biogeochemical cycles usually
translates into carbon cycle.
Ruddiman (2001)
7
Carbon-Cycle Characteristic Timescales
Reservoir Sizes in Gt C Fluxes in Gt C / yr
Sundquist (1993, Science)
8
Average surface- Water composition CO2 0.5
HCO3- 89.0 CO32- 10.5
Thurman Trujillo (2002)
9
Biological Productivity in the Ocean
Nutrients P, N, (Si, Fe)
Ruddiman (2001)
10
The Biological Pump
Atmosphere
CO
2
CO
2
Primary Production
Inorgan. C
Organ. C

Particle-Flux
Ocean
Remineralisation
Organ. C
CO

2
Sediments
Fig. courtesy of A. Körtzinger
11
Photic Zone
Aphotic Zone
Sediments
12
Biogenic Calcium Carbonate Production Raises
Dissolved CO2 Concentration
pH Reaction
(1) Biogenic carbonate uptake
(2) More bicarbonate dissociates
(3) More CO2 is formed
13
The Calcium Carbonate Pump
Atmosphere
CO
2
CO
2
Biogenic CaCO3
Formation
3
Lysocline
Ocean
CaCO3 Dissolution
CO
2-
3
Fig. courtesy of A. Körtzinger
14
Reservoir or Box Models
  • Reservoir an amount of material defined by
    certain physical, chemical or biological
    characteristics that, under the particular
    consideration, can be regarded as homogeneous.
    (Examples CO2 in the atmosphere, Carbon in
    living organic matter in the oceanic surface
    layer)
  • Flux the amount of material transferred from
    one reservoir to another per unit time

15
Single Reservoir Case
Reservoir (mass M)
Flux In
Flux Out
16
Basic Math of Box Models
  • (Rate of change of mass in reservoir)
  • (Flux in) (Flux out) Sources Sinks
  • Or, for concentration (C mol/m3) and water flux
    (Q m3/s)

17
Numerical Solution of Box-Model Equations
Solution by finite-difference method
(approximation!) Euler Method
Initial Condition
Time (in steps of Dt)
18
Numerical Solution of Box-Model Equations
Solution by finite-difference method
(approximation!)
Initial Condition
19
Numerical Solution of Box-Model Equations
Solution by finite-difference method
(approximation!) Euler Method
Initial Condition
Time (in steps of Dt)
20
Euler Method

M
M(tn1)


Prediction

Slope Fi(tn) - Fo(tn) SMS(tn)
Error



True Value

M(tn)


Dt


tn

tn1


t


Assumption Slope at time tn remains constant
throughout time interval Dt
21
Coupled Reservoirs
F12
Reservoir 1 (mass M1)
Reservoir 2 (mass M2)
F21
Principle of mass-conservation requires M1 M2
const.
22
Large-Scale Ocean Circulation
(after Broecker, 1991)
23
(No Transcript)
24
Box-Model ofOceanic PO4 Distribution
Atlantic
Indo-Pacific
Southern Ocean
Surface (0-100 m)
AABW_P (20 Sv)
NADW (10 Sv)
20 Sv
20 Sv
10 Sv
Deep (gt 100 m)
AABW_A (4 Sv)
25
www.geo.uni-bremen.de/geomod/staff/mschulz/lehre/E
COLMAS_Modeling/ bm1_po4_only.gsp
26
Box-Model Experiment 1
  • Vary the water transports and initial PO4
    concentration and observe the final PO4
    concentration and evolution (time series).
  • Q1 How does the final PO4 distribution depend on
    these settings?
  • Q2 How do these settings affect the time it
    takes to reach a steady state? (What
    characterizes the steady state?)

27
Inducing PO4 Gradients Biological Productivity
  • Assume an average export production of
  • 12 g C/m2/yr
  • With a Redfield ratio of CP 1171 (molar
    ratio) and 1 mol C 12 g C
  • ? Corresponding biological PO4 fixation is
  • 1/117 mol P/m2/yr

28
Box-Model of Oceanic PO4 Distribution with
Productivity
Indo-Pacific
Southern Ocean
Atlantic
Surface (0-100 m)
AABW_P (20 Sv)
NADW (10 Sv)
Deep (gt 100 m)
AABW_A (4 Sv)
Assumption Biologically fixed PO4 sinks from the
surface layer to the underlying deep layer, where
the organic material is completely remineralized.
29
www.geo.uni-bremen.de/geomod/staff/mschulz/lehre/E
COLMAS_Modeling/ bm1_po4_fix_prod.gsp
30
Box-Model Experiment 2
  • Q How does the inclusion of biological
    productivity affect the PO4-concentration
    difference between Atlantic and Indo-Pacific
    Oceans in the standard case?

31
10 m water depth
32
1750 m water depth
33
Box-Model Experiment 2
  • Vary the water transports (try max. and small
    values) and observe how the PO4 distribution
    changes. Explain the changes.
  • Q What happens if NADW 0 Sv? (Keep the
    remaining parameters at their default values.)
    Does this result make sense in the real world?
  • Q For which initial PO4 concentration do no
    negative concentrations result (with NADW 0
    Sv)? Is this a reasonable increase for Late
    Pleistocene glacials?

34
Avoiding Negative PO4 Concentrations
Nutrient-Dependent Productivity
  • Assume that productivity scales with the PO4
    availability in the surface layer (variety of
    relationships are possible linear, non-linear
    with saturation)
  • PO4 fixation PO4sfc Volsfc / t mol/yr,
  • where t is the residence time of PO4 in the
    surface due to biological productivity
  • Assume tATL tIPAC 5 yr and tSOC 50 yr
    (Broecker and Peng, 1986)

35
www.geo.uni-bremen.de/geomod/staff/mschulz/lehre/E
COLMAS_Modeling/ bm1_po4_dyn_prod.gsp
36
Box-Model Experiment 3a
  • Run the model for NADW of 0 and 10 Sv and write
    down the PO4 concentrations for the Atlantic
    boxes for each case.
  • Calculate the difference between conc. in deep
    and surface box. What do you observe?

37
Box-Model Experiment 3a Atlantic
NADW (Sv) PO4 Surface (mmol/l) PO4 Deep (mmol/l) DPO4 (mmol/l)
10 0.24 0.69 0.45
0 0.18 0.88 0.70
Shift of PO4 content from surface to deep
Atlantic as NADW drops
38
Box-Model Experiment 3b
  • Run the model for NADW 0, 5, 10, 15, 20 Sv
    and write down the final PO4 fixation in the
    Atlantic Ocean.
  • Sketch NADW vs. PO4 fixation.
  • QWhat is the paleoceanographic implication of
    this finding?

39
NADW and Productivity in the Atlantic Ocean
3.6
3.4
3.2
3
2.8
PO4 Fixation 1011 mol P /yr
2.6
2.4
2.2
2
0
5
10
15
20
NADW Flow Sv
40
Including the Marine Carbon-Cycle
  • Tracers PO4 (? controls productivity)
  • DIC (dissolved inorganic carbon)
  • ALK (alkalinity)
  • Aqueous CO2 partial pressure f(DIC, ALK)
  • Redfield ratio of organic matter (CNP
    117161)
  • Ratio between Corg and CaCO3 production (rain
    ratio) ? assumed to be temperature dependent (a
    crude parameterization of ecosystem dynamics)

41
Rain-Ratio Parameterization
42
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43
Area-Weighted Average
Atmospheric pCO2 Mean Oceanic pCO2
www.geo.uni-bremen.de/geomod/staff/mschulz/lehre/E
COLMAS_Modeling/ bm1_c-cycle_fix_prod.gsp
44
Box-Model Experiment 4C-Cycle with Fixed
Productivity
  • Run the model for the default setting. Identify
    the sources and sinks with respect to atmospheric
    CO2.
  • Run the model for NADW of 0 and 10 Sv. Write down
    the final global mean pCO2 and the productivity
    in the Atlantic Ocean. (Neglect the negative PO4
    conc., identified in the previous exp.)

45
Box-Model Experiment 4C-Cycle with Fixed
Productivity
NADW (Sv) Prod. ATL (Pg C/yr) Prod. Glob. (Pg C/yr) Global pCO2 (ppm)
10 0.447 5.03 281
0 0.447 5.03 265
16 ppm Reduction
46
Box-Model Experiment 5C-Cycle with Dynamic
Productivity
  • How will the response of the mean pCO2 change if
    productivity is no longer constant but a function
    of PO4?

47
www.geo.uni-bremen.de/geomod/staff/mschulz/lehre/E
COLMAS_Modeling/ bm1_c-cycle_dyn_prod.gsp
48
Box-Model Experiment 5C-Cycle with Dynamic
Productivity
  • Run the model for again for NADW of 0 and 10 Sv.
    Write down the final global mean pCO2 and the
    productivity in the Atlantic Ocean.
  • Interpret your results.

49
Box-Model Experiment 5C-Cycle with Dynamic
Productivity
NADW (Sv) Prod. ATL (Pg C/yr) Prod. Glob. (Pg C/yr) Global pCO2 (ppm)
10 0.447 5.03 281
0 0.350 4.83 275
Only 6 ppm Reduction
50
Box-Model Experiment 5C-Cycle with Dynamic
Productivity
NADW 0 ? DIC shifted from surface to deep
Atlantic ? pCO2 reduced BUT PO4 is shifted to
deep ocean too ? less nutrients in surface ?
productivity decreases ? biological pump weakens
? pCO2 increases ? Negative Feedback Mechanism
51
From Box-Models to 2D/3D-Models
Ruddiman (2001)
52
Structure of a Global Biogeo-chemical Model
Ridgwell (2001, Thesis)
53
Modeling Deep-Sea Sediments
Ridgwell (2001, Thesis)
54
Phosphate in the Atlantic Ocean mmol/l
2D-Model (Zonal Mean)
(Schulz and Paul, 2004)
3D-Model (N-S Section)
(Heinze et al., 1999)
55
Horizontal Resolution in a 2D-Biogeochemical Model
(Schulz and Paul, 2004)
56
Horizontal Resolution in a 3D-Biogeochemical Model
(Heinze et al., 1999)
57
A Modeled Sediment Stack in the North Atlantic
Heinze, C. et al., 1999 A global oceanic
sediment model for long-term climate studies.
Global Biogeochemical Cycles, 13, 221-250.
58
Modeled and Observed Modern CaCO3 Content of
Deep-Sea Sediments
Model
Observations
? Even the most sophisticated biogeochemical
models allow only for a crude approximation of
the real world. Discrepancies are largely due to
an inadequate resolution (e.g. MOR) and a lack of
knowledge of the processes being involved.
Heinze et al. (1999)
59
Marine Ecosystem Models Why?
  • Productivity may depend on more than a single
    nutrient (N, P, Si, Fe)
  • Export production controlled by ecosystem
    dynamics
  • Understanding the preferential growth of
    different algae groups (e.g. diatoms vs.
    coccolithophores)
  • Disentangling the seasonal imprint in biological
    proxy records

60
NPZD-Type Ecosystem Model
  • 4 Compartments
  • Coupled to carbon and alkalinity
  • Nutrients are transported by ocean circulation
  • Efficient in predicting seasonal patterns

(after Fasham et al., 1990)
61
Marine Ecosystem Model Components (Moore et al.,
2002)
62
Marine Ecosystem Model Forcing
Output from global OGCM
63
Global Foraminifera Model
Fraile et al. (subm.)
64
Fraile et al. (subm.)
65
Modeled / Observerd Distribution of N. pachyderma
(sin.)
Fraile et al. (subm.)
Brown University Foraminiferal Database (Prell et
al., 1999)
66
Modeled / Observerd Distribution of N. pachyderma
(dex.)
Fraile et al. (subm.)
Brown University Foraminiferal Database (Prell et
al., 1999)
67
Modeled / Observerd Distribution of G. bulloides
Fraile et al. (subm.)
Brown University Foraminiferal Database (Prell et
al., 1999)
68
Modeled / Observerd Distribution of G. ruber
(white)
Fraile et al. (subm.)
Brown University Foraminiferal Database (Prell et
al., 1999)
69
Modeled / Observerd Distribution of G. sacculifer
Fraile et al. (subm.)
Brown University Foraminiferal Database (Prell et
al., 1999)
70
Modeled LGM shift in seasonality of G. bulloides
Fraile et al. (subm.)
71
Benefits of Paleoecosystem Modeling
  • To facilitate model-data comparison
  • To obtain a mechanistic understanding of
    reconstructed shifts in species
  • To assess the potential effect of altered
    plankton successions on proxy reconstructions
    based on organisms
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