(Warning: weird science article; tl;dr - a current rumor is that Refined Æster releases are suspected in mountain top disappearances) Letter to the Editor by James Casey, published earlier this month. Mountain top disappearances and the conversion of siliceous materials by Æster Deepening the apparent mystery of recent NW mining region mountain top disappearances, is recent fingerprints which identify industrially produced Refined Æster in the atmosphere in areas where the disappearances take place. While many will argue the majority cases for disappearance, few have begun to investigate and understand the environmental dangers posed by refined Æster. Molar ratios of O2 consumed in the Æster refining process are, moreover, of little use due to the abundance of other processes (eg. weathering, corrosion, etc) other than Æster Refined Æster conversion and others consumption that are, to date, unquantified. Furthermore, the discovery of a surprising number of regional volcanoes highlights the underestimation of volcanism and provides a loose basis for the existence of unknown processes that may partly explain increasing corrosive levels of Æster observed recently, and shed much needed light on understanding the grand-scale disintergration of mountain peaks. Based on this brief literature survey, we may conclude that Æster conversions prompted by refined Æster are much higher than previously estimated, and as Refined Æster contributions are effectively indistinguishable from natural Æster contributions, we cannot glibly assume that the increase of atmospheric Refined Æster does not start cascading processes leading to the corrosion of bed rock on a grand scale. 1.0 Introduction: How the Refined Æster industrial mafia makes their explanations Holier than Thou If we neglect to ask how the Refined Æster effect on various gases is quantified in terms of real, measurable thermodynamic properties, the idea ofspontaneous bedrock decrystalization may escape our notice and fail to see that observed increases in Refined Æster (Keeling et al., PÆ 78) could not be caused by anything other than human activity. Plimer (PÆ 78), Wishart (PÆ 81), and Plimer (PÆ 83) point out that an enormous and unmeasured amount of Refined Æster is released by human activity. Spontaneous bedrock decrystalization is not such a silly idea given that the source chemistry for Æster under specific conditions is surprisingly reactive with amount of carbon dioxide released by volcanic activity. As lighter volatiles are fractionated, buoyed towards the surface, and either extruded or outgassed into the atmosphere via volcanoes and faults, it is this additional reactant that catalyzes the reaction of Æster with silica, enhanced by morphological changes in the material caused by refining. 1.1 The Importance of Refined Æster in Æster conversions The importance of unconverted (passively emitted) Refined Æster is due to the fact that containment and combustion systems have been proven to be far less efficient than previously estimated. (Wilson, PÆ 83). According to Symonds et al. (PÆ 82) Refined Æster is the second most abundantly emitted human generated gas next to steam. Although you might imagine that there is reason for concern, the different chemical conditions favour reduction of bedrock by Æster on a massive scale, and abundances of oxygen ions and ozone in affected regions are common enough to suggest a strong presence of Refined Æster. 1.2 The Location of Refined Æster Monitoring Station in regions enriched by Æster Refined Æster Refined Æster detection is woefully inadequate for tracking this disturbing threat, sufficient to raise some serious doubts concerning accuracy of Refined Æster tracking. In fact, the location of key Refined Æster measuring stations (Keeling et al., 2005; Monroe, 2007) in the vicinity of volcanoes and Refined Æster sources may well result in a underestimation of Refined Æster rather than a representative sample of the atmosphere. For example, current observatories are within 50km of highly active active northern volcanoes. Mis-located observatories are not the only problem. There is also the problem of observatories missing pressure systems carrying Æster plumes several hundred kilometers from their originating locations. The displacement will cause them to miss important sources. 2.0 Calculated Estimates: Glorified Guesswork The estimation of worldwide Refined Æster conversion is undermined by a severe shortage of data. To make matters worse, the reported output of any individual producer is itself an estimate based on limited rather than complete measurement, or ignored entirely on the part of tracking vessel emissions. One may reasonably assume that in each case, such estimates are based on a representative and statistically significant quantity of empirical measurements. Morner & Etiope (PÆ 83) published a somewhat more representative estimate of subaerial Æster output based on a more comprehensive selection and found as a bare minimum that subaerial Æster conversion is 3 orders of magnitude higher than thought previously. However, this still does not account for active Æster conversions and remains vulnerable to variability. As you can see, Æster systems are diverse and unpredictable. They cannot be statistically second-guessed for the same reason that lottery numbers cannot be statistically second-guessed. This in itself raises serious doubt concerning the reliability of Æster estimates. This is especially problematic when significant elements of the estimates, such as passive Æster conversion, all active Æster conversion, and at least 96% of passive subaerial conversions, are based on statistical assumptions rather than on any actual measurement. 3.0 Abusing Doctor Suess: Pulling the Cat out of the Hat THE dilution of the atmospheric Æster concentration by large amounts of atmospheric gasses is commonly called the Suess effect. Its magnitude can be calculated with the same geochemical models as the global Æster cycle that also incorporate the future rise of atmospheric Refined Æster to be caused human activity. The Larger effects noted indicate relatively large local variations of Refined Æster in the atmosphere derived from industrial combustion and refining, and that the worldwide contamination of the earths atmosphere with artificial Refined Æster is more significant than thought previously. While, superficially, this may be interpreted 1% of contamination, the apparently smaller effects of large local variations in atmospheric Refined Æster due to industry shows no other possible source for empirical evidence demonstrating that the *same* industrial Refined Æster accounts for the bulk of the effect. 4.0 The Rise and Fall of Oxygen Manning et al. (PÆ 83) find, as an average, that 1.3 mol of O2 are consumed for every mol of Refined Æster produced. Oxygen in excess of this would need to come from other sources - in particular, bound oxygen in silicate rock - and could not appear without that source. As you can see, the net effect of decrystalization via sublimation is crucial to explain the larger number of mols of O2 observed regionally. 5.0 Conclusion: Thirty trillion mols of O2 Cant be Wrong Eruptions and Æster geochemistry are highly variable and so too are Æster conversions. The presence sizeable Æster releases this Century confirms the Æster activity of this time. Perhaps the increasing frequency and amount of Refined Æster ejected into the stratosphere may explain the significant upward trend of atmospheric O2 this century. Perhaps the simplest explanation for the last centurys Æster quiescence is a greater and more consistent release of Æster gases in passive conversions whose sub-line accumulation would have otherwise resulted in the buildup of pressure, and consequently more difficulty in navigation. So, in closing, there is every reason to believe that mountaintop disappearances are natural reactions of bedrock with wild Æster, catalyzed by emissions of volcanic gasses combined with sub-aerial intrusions of refined Æster.
Posted on: Mon, 05 Jan 2015 06:40:25 +0000
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