Blockbuster Paper Finds Just 15% Of CO2 Growth Since Industrialization Is Due To Human Emissions
By Kenneth Richard on 25. February 2017
Has the IPCC made a profoundly flawed assumption?
Take a look at what Kenneth has just found. This very new paper that follows has just been published, and will certainly raise a lot of eyebrows in the climate science field. It turns out that the human CO2 contribution in the atmosphere may very well have been hugely overstated. -PG
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CO2 Has Risen By 110 ppm Since 1750 The Human Contribution Is Just 17 ppm 
Harde, 2017Abstract:Climate scientists presume that the carbon cycle has come out of balance due to the increasing anthropogenic emissions from fossil fuel combustion and land use change. This is made responsible for the rapidly increasing atmospheric CO2 concentrations over recent years, and it is estimated that the removal of the additional emissions from the atmosphere will take a few hundred thousand years. Since this goes along with an increasing greenhouse effect and a further global warming, a better understanding of the carbon cycle is of great importance for all future climate change predictions. We have critically scrutinized this cycle and present an alternative concept, for which the uptake of CO2 by natural sinks scales proportional with the CO2 concentration. In addition, we consider temperature dependent natural emission and absorption rates, by which the paleoclimatic CO2 variations and the actual CO2 growth rate can well be explained. The anthropogenic contribution to the actual CO2 concentration is found to be 4.3%, its fraction to the CO2 increase over the Industrial Era is 15% and the average residence time 4 years.
Conclusion:Climate scientists assume that a disturbed carbon cycle, which has come out of balance by the increasing anthropogenic emissions from fossil fuel combustion and land use change, is responsible for the rapidly increasing atmospheric CO2 concentrations over recent years. While over the whole Holocene up to the entrance of the Industrial Era (1750) natural emissions by heterotrophic processes and fire were supposed to be in equilibrium with the uptake by photosynthesis and the net oceanatmosphere gas exchange, with the onset of the Industrial Era the IPCC estimates that about 15 – 40 % of the additional emissions cannot further be absorbed by the natural sinks and are accumulating in the atmosphere.
The IPCC further argues that CO2 emitted until 2100 will remain in the atmosphere longer than 1000 years, and in the same context it is even mentioned that the removal of human-emitted CO2 from the atmosphere by natural processes will take a few hundred thousand years (high confidence) (see AR5-Chap.6-Executive-Summary).
Since the rising CO2 concentrations go along with an increasing greenhouse effect and, thus, a further global warming, a better understanding of the carbon cycle is a necessary prerequisite for all future climate change predictions. In their accounting schemes and models of the carbon cycle the IPCC uses many new and detailed data which are primarily focussing on fossil fuel emission, cement fabrication or net land use change (see AR5-WG1-Chap.6.3.2), but it largely neglects any changes of the natural emissions, which contribute to more than 95 % to the total emissions and by far cannot be assumed to be constant over longer periods (see, e.g.: variations over the last 800,000 years (Jouzel et al., 2007); the last glacial termination (Monnin et al., 2001); or the younger Holocene (Monnin et al., 2004; Wagner et al., 2004)).
Since our own estimates of the average CO2 residence time in the atmosphere differ by several orders of magnitude from the announced IPCC values, and on the other hand actual investigations of Humlum et al. (2013) or Salby (2013, 2016) show a strong relation between the natural CO2 emission rate and the surface temperature, this was motivation enough to scrutinize the IPCC accounting scheme in more detail and to contrast this to our own calculations.
Different to the IPCC we start with a rate equation for the emission and absorption processes, where the uptake is not assumed to be saturated but scales proportional with the actual CO2 concentration in the atmosphere (see also Essenhigh, 2009; Salby, 2016). This is justified by the observation of an exponential decay of 14C. A fractional saturation, as assumed by the IPCC, can directly be expressed by a larger residence time of CO2 in the atmosphere and makes a distinction between a turnover time and adjustment time needless. Based on this approach and as solution of the rate equation we derive a concentration at steady state, which is only determined by the product of the total emission rate and the residence time. Under present conditions the natural emissions contribute 373 ppm and anthropogenic emissions 17 ppm to the total concentration of 390 ppm (2012). For the average residence time we only find 4 years.
The stronger increase of the concentration over the Industrial Era up to present times can be explained by introducing a temperature dependent natural emission rate as well as a temperature affected residence time. With this approach not only the exponential increase with the onset of the Industrial Era but also the concentrations at glacial and cooler interglacial times can well be reproduced in full agreement with all observations. So, different to the IPCC’s interpretation the steep increase of the concentration since 1850 finds its natural explanation in the self accelerating processes on the one hand by stronger degassing of the oceans as well as a faster plant growth and decomposition, on the other hand by an increasing residence time at reduced solubility of CO2 in oceans.
Together this results in a dominating temperature controlled natural gain, which contributes about 85 % to the 110 ppm CO2 increase over the Industrial Era, whereas the actual anthropogenic emissions of 4.3 % only donate 15 %. These results indicate that almost all of the observed change of CO2 during the Industrial Era followed, not from anthropogenic emission, but from changes of natural emission.
The results are consistent with the observed lag of CO2 changes behind temperature changes (Humlum et al., 2013; Salby, 2013), a signature of cause and effect. Our analysis of the carbon cycle, which exclusively uses data for the CO2 concentrations and fluxes as published in AR5, shows that also a completely different interpretation of these data is possible, this in complete conformity with all observations and natural causalities.
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