340 likes | 507 Views
GEOF236 CHEMICAL OCEANOGRAPHY (HØST 2012) Christoph Heinze University of Bergen, Geophysical Institute and Bjerknes Centre for Climate Research Prof. in Global Carbon Cycle Modelling Allegaten 70, N-5007 Bergen, Norway Phone: +47 55 58 98 44 Fax: +47 55 58 98 83
E N D
GEOF236 CHEMICAL OCEANOGRAPHY (HØST 2012) ChristophHeinze University of Bergen, Geophysical Institute and Bjerknes Centre for Climate Research Prof. in Global Carbon Cycle Modelling Allegaten 70, N-5007 Bergen, Norway Phone: +47 55 58 98 44 Fax: +47 55 58 98 83 Mobile phone: +47 975 57 119 Email: christoph.heinze@gfi.uib.no DEAR STUDENT AND COLLEAGUE: ”This presentation is for teaching/learning purposes only. Do not useany material ofthispresentation for any purpose outsidecourse GEOF236, ”Chemical Oceanography”, autumn 2012, Universityof Bergen. Thankyou for yourattention.”
Sarmiento&Gruber 2006 Chapter 9: Calcium carbonate cycle, part 2
Carbon pumps SOLUBILITY Heinze, C., E. Maier-Reimer, and K. Winn, 1991, Glacial pCO2 reduction by the World Ocean - experiments with the Hamburg Carbon Cycle Model, Paleoceanography, 6, 395-430.
Carbon in seawater: CO2 added, carbonate saturation The major factor for changing TA is precipitation/dissolutionof CaCO3: CaCO3solid↔ Ca2+ +CO32- calcium carbonate (calcite, aragonite) So in principle one can neutralise CO2gas by dissolving CaCO3: CaCO3solid + CO2gas + H2O ↔ Ca2++ 2HCO3- Over-/undersaturation with respect to CaCO3 is determined by the solubility product: Ksp = [Ca2+ ]sat x [CO32-]sat = const. x [CO32-]sat Therefore: By adding CO2 we decrease the carbonate saturation. Ω = saturation state = ([CO32-]actual ∙[Ca2+]actual)/Ksp ≈ [CO32-]actual/ [CO32-]sat
Carbon pumps Source: Zeebe & Wolf-Gladrow, 2001
Two different concepts to discriminate between over- and undersaturated areas: Lysocline: Depth interval , where CaCO3 shell material undergoes strong signs of corrosion. Calcium carbonate compensation depth, CCD: depth level, where rain and re-dissolution balance. Therefore: Below the CCD there is no CaCO3 available anymore. Tucker and Wright (1990)
Atlantic Pacific Model Observation GEOSECS Black dots: approximate saturation depth level, using the critical CO32- concentration)
Diagenesis model: • Model to predict: • solid concentrations in the bioturbated zone • porewater concentrations in the bioturbated zone • flux of dissolved constituents between water column and porewaters • Burial of solid material to “stone” • SEE ARCHER ET AL. 1993
Diagenesis modelling: Heinze et al., 2009, Paleoceanography
Diagenesis modelling: Heinze et al., 2009, Paleoceanography
CaCO3 from Eq. Pac. Farrell&Prell 1989 last 130,000 years Atmosph. CO2 Siegenthaler et al., 2005
Tracer signals – example Atlantic Balsam 1983 Pazific Farrell & Prell 1989
Zachos et al., 2005 http://www.fossilmuseum.net/GeologicalTimeMachine.htm
T anomaly across the Paleocene-Eocene boundary (Winguth et al., 2010)
Direct measurements of Cant in the ocean: Sarmiento&Gruber, 2006
Direct measurements of Cant in the ocean: Santana-Casiano et al., GBC, 2007
Potential alterations in biological cycling of carbon with circulation and pCO2 change: 350 μatm (green)700 μatm (grey)1050 μatm (red) Mesocosm experiments at differing atmospheric pCO2: ”Captering natural ecosystem communities in plastic bags and watching their behavior for changes in forcing under controlled conditions” Apparent decrease of dissolved inorganic C with pCO2 Apparent increase of organically bound C with pCO2 Apparent increase of nutrient utilisiation efficiency with pCO2 Riebesell, Schulz, Bellerby, Botros, Fritsche, Meyerhöfer, Neill, Nondal, Oschlies, Wohlers & Zöllner, Nature, 2007 Mesocosm facilities at Espegrend, Bergen
PTEROPODS (small snails) (aragonite producers) Antarctic pteropod, Fabry et al., Oceanography, 2009 CORALS (aragonite producers) Hoegh-Guldberg et al., Science, 2007
Anthroogenic CO2emssion scenarios: Raupach et al., 2007, PNAS
Aragonite saturation according to future climate projections:
Aragonite saturation according to future climate projections: Steinacher et al., Biogeosciences, 2009
CaCO3 sediment can start to dissolve close to deep-water production areas due to anthropogenic CO2: Gehlen et al., 2008
CaCO3 sediment can start to dissolve close to deep-water production areas due to anthropogenic CO2: Gehlen et al., 2008
CaCO3 sediment can start to dissolve close to deep-water production areas due to anthropogenic CO2: Gehlen et al., 2008
Ocean is central for long-term uptake and storage of anthropogenic CO2: CaCO3 sediment neutralises without CaCO3 sediment with IPCC AR4, Ch. 7, following Archer, 2005 Core top CaCO3 Archer, 1996
Warm water corals Guinotte&Fabry, 2008
Deep water corals Guinotte&Fabry, 2008