Increase in stomatal size, S, in response to growth at elevated atmospheric CO2 (short-term experiments)
|
Plants |
Table - link |
N/A |
116579 |
Franks PJ, Beerling DJ.... |
Standard redox potential of CO2 to acetate
|
Unspecified |
-290 |
mV |
104403 |
Harold L. Drake, Kirsten... |
Redox potential for carbohydrate unit (CO2/CH2O)
|
Generic |
-430 |
mV |
104604 |
Paul G. Falkowski, John... |
Ratio of RuBisCO carboxylation to oxygenation at CO2 level of 210 ppm
|
Biosphere |
0.41 |
unitless |
111971 |
Sharkey T.D. (1988) ... |
CO2 produced by various metabolic reactions and refixed by RuBisCO
|
Bacteria Rhodopseudomonas palustris |
Table - link |
N/A |
109363 |
McKinlay JB, Harwood... |
Fermentation excretion rate of CO2 and formate
|
Bacteria Salmonella typhimurium |
12.5 to 28.7 Table - link |
mmol/g/hour |
109676 |
Driessen M, Postma PW... |
Mitochondrial counts of plants grown in elevated and ambient atmospheric CO2 partial pressures
|
Plants |
Table - link |
N/A |
103081 |
Griffin KL, Anderson OR... |
Typical stromal HCO3– concentration apparently required for CCM (CO2 concentrating mechanism) function
|
Green algae Chlamydomonas reinhardtii |
2 – 3 |
mM |
114619 |
Wang Y, Stessman DJ,... |
Doubling time in initial CO/CO2 ratio of 1.4
|
Bacteria Clostridium thermoautotrophicum |
7 |
hours |
105526 |
Savage MD, Wu ZG, Daniel SL... |
CO2 budget of atmosphere in mol x 10^14/year and CO2 exchange in mol 10^14/year, between the atmosphere, rivers and the world oceans
|
Biosphere |
Table - link |
mol CO2 x 10^14/year |
116104 |
Duursma EK, Boisson MPRM... |
Acceleration rate of hydration of CO2 by carbonic anhydrase
|
Human Homo sapiens |
~14,000 |
fold |
110584 |
Forster RE, Gros G, Lin L... |
Estimated cumulative oceanic anthropogenic CO2 sink in 1994, for the ocean region
|
Biosphere |
118 (±19) |
PgC |
108707 |
Sabine CL et al., The... |
Growth enhancements in response to elevated CO2 reported in different reviews
|
Plants |
Table - link |
% |
110846 |
Kirschbaum MUF (2011)... |
Fraction of fructose 1,6-bisphosphate that is channelled to CO2
|
Bacteria Escherichia coli |
99 (±16) |
% |
110834 |
Shearer G, Lee JC, Koo JA... |
Chloroplast fine structure of plants grown in elevated and ambient atmospheric CO2 partial pressures
|
Plants |
Table - link |
N/A |
103082 |
Griffin KL, Anderson OR... |
Photorespiration fraction of photosynthesis at chloroplast CO2 levels corresponding to current atmospheres above 30˚C–35˚C
|
C3 plants |
>25 |
% |
111968 |
Sage RF, Sage TL, Kocacinar... |
Fraction of assimilated CO2 that is further released in mitochondria by photorespiratory pathway
|
Unspecified |
~30 |
% |
114215 |
Zhao H et al., Kinetic... |
Maximum photosynthetic rates under strong illumination and high CO2 concentrations
|
Spinach Spinacia oleracea |
200-500 |
µmol reduced CO2/(mg chlorophyll×hour) |
103396 |
Karl-Josef Dietz and... |
Quantities of the greenhouse gas CO2 that the ocean is able to absorb
|
Biosphere |
~37,000 |
Gt CO2 |
113986 |
Danovaro R et al., Marine... |
Membrane permeability to CO2 of four species of diatoms and of artificial lipid membranes
|
Diatoms |
0.015 cm/sec - 0.056 cm/sec artificial lipid membranes ~0.1 |
cm/sec |
116872 |
Hopkinson BM, Dupont CL... |