WR - View Single Post - Cheney’s Office Pressured EPA Over Regulating Greenhouse Gases

Quote:

Determinations of CO2 in polar ice cores are commonly used for estimations of the pre-industrial CO2 atmospheric levels. Perusal of these determinations convinced me that glaciological studies are not able to provide a reliable reconstruction of CO2 concentrations in the ancient atmosphere. This is because the ice cores do not fulfill the essential closed system criteria. One of them is a lack of liquid water in ice, which could dramatically change the chemical composition the air bubbles trapped between the ice crystals. This criterion, is not met, as even the coldest Antarctic ice (down to -73°C) contains liquid water[2]. More than 20 physico-chemical processes, mostly related to the presence of liquid water, contribute to the alteration of the original chemical composition of the air inclusions in polar ice[3].

One of these processes is formation of gas hydrates or clathrates. In the highly compressed deep ice all air bubbles disappear, as under the influence of pressure the gases change into the solid clathrates, which are tiny crystals formed by interaction of gas with water molecules. Drilling decompresses cores excavated from deep ice, and contaminates them with the drilling fluid filling the borehole. Decompression leads to dense horizontal cracking of cores, by a well known sheeting process. After decompression of the ice cores, the solid clathrates decompose into a gas form, exploding in the process as if they were microscopic grenades. In the bubble-free ice the explosions form a new gas cavities and new cracks[4]. Through these cracks, and cracks formed by sheeting, a part of gas escapes first into the drilling liquid which fills the borehole, and then at the surface to the atmospheric air. Particular gases, CO2, O2 and N2 trapped in the deep cold ice start to form clathrates, and leave the air bubbles, at different pressures and depth. At the ice temperature of -15°C dissociation pressure for N2 is about 100 bars, for O2 75 bars, and for CO2 5 bars. Formation of CO2 clathrates starts in the ice sheets at about 200 meter depth, and that of O2 and N2 at 600 to 1000 meters. This leads to depletion of CO2 in the gas trapped in the ice sheets. This is why the records of CO2 concentration in the gas inclusions from deep polar ice show the values lower than in the contemporary atmosphere, even for the epochs when the global surface temperature was higher than now.

The data from shallow ice cores, such as those from Siple, Antarctica[5, 6], are widely used as a proof of man-made increase of CO2 content in the global atmosphere, notably by IPCC[7]. These data show a clear inverse correlation between the decreasing CO2 concentrations, and the load-pressure increasing with depth (Figure 1 A) . The problem with Siple data (and with other shallow cores) is that the CO2 concentration found in pre-industrial ice from a depth of 68 meters (i.e. above the depth of clathrate formation) was "too high". This ice was deposited in 1890 AD, and the CO2 concentration was 328 ppmv, not about 290 ppmv, as needed by man-made warming hypothesis. The CO2 atmospheric concentration of about 328 ppmv was measured at Mauna Loa, Hawaii as later as in 1973[8], i.e. 83 years after the ice was deposited at Siple.

An ad hoc assumption, not supported by any factual evidence[3, 9], solved the problem: the average age of air was arbitrary decreed to be exactly 83 years younger than the ice in which it was trapped. The "corrected" ice data were then smoothly aligned with the Mauna Loa record (Figure 1 B) , and reproduced in countless publications as a famous "Siple curve". Only thirteen years later, in 1993, glaciologists attempted to prove experimentally the "age assumption"[10], but they failed[9].

Don't know what I'm talking about indeed.

Note the presence of liquid water invalidates CO2 measurements.