scholarly journals Presentation, calibration and validation of the low-order, DCESS Earth System Model

2008 ◽  
Vol 1 (1) ◽  
pp. 39-124
Author(s):  
G. Shaffer ◽  
S. Malskǽr Olsen ◽  
J. O. P. Pedersen

Abstract. A new, low-order Earth system model is described, calibrated and tested against Earth system data. The model features modules for the atmosphere, ocean, ocean sediment, land biosphere and lithosphere and has been designed to simulate global change on time scales of years to millions of years. The atmosphere module considers radiation balance, meridional transport of heat and water vapor between low-mid latitude and high latitude zones, heat and gas exchange with the ocean and sea ice and snow cover. Gases considered are carbon dioxide and methane for all three carbon isotopes, nitrous oxide and oxygen. The ocean module has 100 m vertical resolution, carbonate chemistry and prescribed circulation and mixing. Ocean biogeochemical tracers are phosphate, dissolved oxygen, dissolved inorganic carbon for all three carbon isotopes and alkalinity. Biogenic production of particulate organic matter in the ocean surface layer depends on phosphate availability but with lower efficiency in the high latitude zone, as determined by model fit to ocean data. The calcite to organic carbon rain ratio depends on surface layer temperature. The semi-analytical, ocean sediment module considers calcium carbonate dissolution and oxic and anoxic organic matter remineralisation. The sediment is composed of calcite, non-calcite mineral and reactive organic matter. Sediment porosity profiles are related to sediment composition and a bioturbated layer of 0.1 m thickness is assumed. A sediment segment is ascribed to each ocean layer and segment area stems from observed ocean depth distributions. Sediment burial is calculated from sedimentation velocities at the base of the bioturbated layer. Bioturbation rates and oxic and anoxic remineralisation rates depend on organic carbon rain rates and dissolved oxygen concentrations. The land biosphere module considers leaves, wood, litter and soil. Net primary production depends on atmospheric carbon dioxide concentration and remineralization rates in the litter and soil are related to mean atmospheric temperatures. Methane production is a small fraction of the soil remineralization. The lithosphere module considers outgassing, weathering of carbonate and silicate rocks and weathering of rocks containing old organic carbon and phosphorus. Weathering rates are related to mean atmospheric temperatures. A pre-industrial, steady state calibration to Earth system data is carried out. Ocean observations of temperature, carbon 14, phosphate, dissolved oxygen, dissolved inorganic carbon and alkalinity constrain air-sea exchange and ocean circulation, mixing and biogeochemical parameters. Observed calcite and organic carbon distributions and inventories in the ocean sediment help constrain sediment module parameters. Carbon isotopic data and carbonate vs silicate weathering fractions are used to estimate initial lithosphere outgassing and rock weathering rates. Model performance is tested by simulating atmospheric greenhouse gas increases, global warming and model tracer evolution for the period 1765 to 2000, as forced by prescribed anthropogenic greenhouse gas inputs and other anthropogenic and natural forcing. Long term, transient model behavior is studied with a set of 100 000 year simulations, forced by a slow, 5000 GtC input of CO2 to the atmosphere, and with a 1.5 million year simulation, forced by a doubling of lithosphere CO2 outgassing.

2008 ◽  
Vol 1 (1) ◽  
pp. 17-51 ◽  
Author(s):  
G. Shaffer ◽  
S. Malskær Olsen ◽  
J. O. Pepke Pedersen

Abstract. A new, low-order Earth System Model is described, calibrated and tested against Earth system data. The model features modules for the atmosphere, ocean, ocean sediment, land biosphere and lithosphere and has been designed to simulate global change on time scales of years to millions of years. The atmosphere module considers radiation balance, meridional transport of heat and water vapor between low-mid latitude and high latitude zones, heat and gas exchange with the ocean and sea ice and snow cover. Gases considered are carbon dioxide and methane for all three carbon isotopes, nitrous oxide and oxygen. The ocean module has 100 m vertical resolution, carbonate chemistry and prescribed circulation and mixing. Ocean biogeochemical tracers are phosphate, dissolved oxygen, dissolved inorganic carbon for all three carbon isotopes and alkalinity. Biogenic production of particulate organic matter in the ocean surface layer depends on phosphate availability but with lower efficiency in the high latitude zone, as determined by model fit to ocean data. The calcite to organic carbon rain ratio depends on surface layer temperature. The semi-analytical, ocean sediment module considers calcium carbonate dissolution and oxic and anoxic organic matter remineralisation. The sediment is composed of calcite, non-calcite mineral and reactive organic matter. Sediment porosity profiles are related to sediment composition and a bioturbated layer of 0.1 m thickness is assumed. A sediment segment is ascribed to each ocean layer and segment area stems from observed ocean depth distributions. Sediment burial is calculated from sedimentation velocities at the base of the bioturbated layer. Bioturbation rates and oxic and anoxic remineralisation rates depend on organic carbon rain rates and dissolved oxygen concentrations. The land biosphere module considers leaves, wood, litter and soil. Net primary production depends on atmospheric carbon dioxide concentration and remineralization rates in the litter and soil are related to mean atmospheric temperatures. Methane production is a small fraction of the soil remineralization. The lithosphere module considers outgassing, weathering of carbonate and silicate rocks and weathering of rocks containing old organic carbon and phosphorus. Weathering rates are related to mean atmospheric temperatures. A pre-industrial, steady state calibration to Earth system data is carried out. Ocean observations of temperature, carbon 14, phosphate, dissolved oxygen, dissolved inorganic carbon and alkalinity constrain air-sea exchange and ocean circulation, mixing and biogeochemical parameters. Observed calcite and organic carbon distributions and inventories in the ocean sediment help constrain sediment module parameters. Carbon isotopic data and carbonate vs. silicate weathering fractions are used to estimate initial lithosphere outgassing and rock weathering rates. Model performance is tested by simulating atmospheric greenhouse gas increases, global warming and model tracer evolution for the period 1765 to 2000, as forced by prescribed anthropogenic greenhouse gas inputs and other anthropogenic and natural forcing. Long term, transient model behavior is studied with a set of 100 000 year simulations, forced by a slow, 5000 Gt C input of CO2 to the atmosphere, and with a 1.5 million year simulation, forced by a doubling of lithosphere CO2 outgassing.


Radiocarbon ◽  
2003 ◽  
Vol 45 (1) ◽  
pp. 17-24 ◽  
Author(s):  
Naohiko Ohkouchi ◽  
Timothy I Eglinton ◽  
John M Hayes

We have measured the radiocarbon contents of individual, solvent-extractable, short-chain (C14, C16, and C18) fatty acids isolated from Ross Sea surface sediments. The corresponding 14C ages are equivalent to that of the post-bomb dissolved inorganic carbon (DIC) reservoir. Moreover, molecular 14C variations in surficial (upper 15 cm) sediments indicate that these compounds may prove useful for reconstructing chronologies of Antarctic margin sediments containing uncertain (and potentially variable) quantities of relict organic carbon. A preliminary molecular 14C chronology suggests that the accumulation rate of relict organic matter has not changed during the last 500 14C yr. The focus of this study is to determine the validity of compound-specific 14C analysis as a technique for reconstructing chronologies of Antarctic margin sediments.


2008 ◽  
Vol 5 (6) ◽  
pp. 1615-1623 ◽  
Author(s):  
S. Fiedler ◽  
B. S. Höll ◽  
A. Freibauer ◽  
K. Stahr ◽  
M. Drösler ◽  
...  

Abstract. Numerous studies have dealt with carbon (C) contents in Histosols, but there are no studies quantifying the relative importance of the individual C components in pore waters. For this study, measurements were taken of all the carbon components (particulate organic carbon, POC; dissolved organic carbon, DOC; dissolved inorganic carbon, DIC; dissolved methane, CH4) in the soil pore water of calcareous fens under three different water management regimes (re-wetted, deeply and moderately drained). Pore water was collected weekly or biweekly (April 2004 to April 2006) at depths between 10 and 150 cm. The main results obtained were: (1) DIC (94–280 mg C l−1) was the main C-component. (2) POC and DOC concentrations in the pore water (14–125 mg C l−1 vs. 41–95 mg C l−1) were pari passu. (3) Dissolved CH4 was the smallest C component (0.005–0.9 mg C l−1). Interestingly, about 30% of the POM particles were colonized by microbes indicating that they are active in the internal C turnover. Certainly, both POC and DOC fractions are essential components of the C budget of peatlands. Furthermore, dissolved CO2 in all forms of DIC appears to be an important part of peatland C-balance.


1973 ◽  
Vol 30 (10) ◽  
pp. 1441-1445 ◽  
Author(s):  
Michael P. Stainton

A simple, rapid method for determining dissolved inorganic carbon in water is described. A 20-cm3 sample of water is drawn into a 50-cm3 polypropylene syringe and acidified by injection of 1 cm3 of dilute sulphuric acid. Twenty-nine cubic centimeters of helium at atmospheric pressure is injected into the syringe followed by 10 sec of manual agitation to partition CO2 between gas and liquid phase. The gas phase containing 60% of CO2 from the sample is then analyzed by gas chromatography. This method has been used to determine dissolved inorganic and organic carbon in Canadian Shield waters and to determine total carbonates in sediments.


2004 ◽  
Vol 64 (3b) ◽  
pp. 583-590 ◽  
Author(s):  
M. B. Cunha-Santino ◽  
I. Bianchini JR.

Assays were carried out to evaluate the dissolved oxygen uptake resulting from mineralization of humic substances (fulvic acid (FA) and humic acid (HA)) from different sources: sediment, dissolved organic matter (DOM) of 120-day decomposed aquatic macrophyte (Scirpus cubensis and Cabomba piauhyensis), and lagoon DOM. The experiments were also aimed at estimating the oxygen uptake coefficient of the mineralization. About 20-30 mg of substrate were added to 1.1 liters of water from Infernão Lagoon (21º33' to 21º37'S; 47º45' to 47º51'W). The solutions were aerated and the dissolved oxygen (DO) was monitored during 40 days. Dissolved organic carbon (DOC) and particulate organic carbon (POC) were estimated after 80 days of the experiment. Anaerobic processes were avoided by aerating the solutions. The results were fitted to a first-order kinetics model, from which the uptake of oxygen parameters was obtained. Oxygen consumption (OC) ranged from 4.24 mg L-1 (HA - S. cubensis) to 33.76 mg L-1 (FA - sediment). The highest deoxygenation coefficient (kD) was observed during mineralization of FA - DOM (0.299 day-1), followed in decreasing order by FA - S. cubensis, HA - sediment, HA - S. cubensis, FA - sediment, and FA - C. piauhyensis (0.282; 0.255; 0.178; 0.130, and 0.123 day-1, respectively). The carbon analyses indicated that the FA and HA samples at the end of the experiment presented a decay that varied from 15.23% to 42.35% and that the FA and HA conversions into POC were relatively low (from 0.76% to 3.94%).


2010 ◽  
Vol 269 (1-2) ◽  
pp. 22-32 ◽  
Author(s):  
Stephen R. Parker ◽  
Christopher H. Gammons ◽  
Simon R. Poulson ◽  
Michael D. DeGrandpre ◽  
Charmaine L. Weyer ◽  
...  

2012 ◽  
Vol 9 (3) ◽  
pp. 1159-1172 ◽  
Author(s):  
A. Gnanadesikan ◽  
J. P. Dunne ◽  
J. John

Abstract. Global warming is expected to reduce oxygen solubility and vertical exchange in the ocean, changes which would be expected to result in an increase in the volume of hypoxic waters. A simulation made with a full Earth System model with dynamical atmosphere, ocean, sea ice and biogeochemical cycling (the Geophysical Fluid Dynamics Laboratory's Earth System Model 2.1) shows that this holds true if the condition for hypoxia is set relatively high. However, the volume of the most hypoxic (i.e., suboxic) waters does not increase under global warming, as these waters actually become more oxygenated. We show that the rise in dissolved oxygen in the tropical Pacific is associated with a drop in ventilation time. A term-by-term analysis within the least oxygenated waters shows an increased supply of dissolved oxygen due to lateral diffusion compensating an increase in remineralization within these highly hypoxic waters. This lateral diffusive flux is the result of an increase of ventilation along the Chilean coast, as a drying of the region under global warming opens up a region of wintertime convection in our model. The results highlight the potential sensitivity of suboxic waters to changes in subtropical ventilation as well as the importance of constraining lateral eddy transport of dissolved oxygen in such waters.


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