Table 1.
CH4 | H2 | CO | OH | (yr) | ||
---|---|---|---|---|---|---|
Steady state | Concentration (ppb) | 1890 | 530 | 80 | 106 cm−3 | |
Sources (ppb/yr) | 226 | 265a | 480a | 1333 | ||
τ (yr) | 8.3 | 2 | 0.17 | 1 s | ||
Linear stability | CH4 mode | 1% | 0.31% | 0.64% | −0.39% | 12.3 |
H2 mode | −0.01% | 1% | 0.03% | −0.06% | 2 | |
CO mode | −0.008% | 0.001% | 1% | −0.36% | 0.2 | |
OH mode | ...b | ...b | ...b | 1% | 1.5 s |
aSources for CO and H2 include production from CH4 oxidation.
b... is <10−7.
Sources are obtained from the system (5)–(8) at steady state with the current tropospheric concentrations. τ is the average lifetime of each gas. The modes are expressed as relative changes normalized so that the dominant species’ ratio is 1%. Reaction rates are defined as follows: k1 = 3.17 × 10−15 cm3/s; k2 = 3.8 × 10−15 cm3/s; k3 = 1.9 × 10−13 cm3/s; ks = 0.02 yr−1; kd = 0.38 yr−1 is such that soil uptake accounts for 75% of atmospheric H2 removal; k4[X] = 0.3 s−1 (EOH = 0.82) is defined so that 45% of OH is consumed by the species X, 36% by CO, 14% by CH4, and 5% by H238. Concentrations are converted to mixing ratios using 1 ppb = 1.57 × 1010 cm−3; sources are converted from ppb/yr to Tg/yr using 4.22 × 1018 kg as the troposphere mass68.