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Originally posted by bluemirage5
reply to post by Aloysius the Gaul
It said ZCS WITH radioactive particles; I'm assuming it was combined
Originally posted by GogoVicMorrow
Originally posted by Aloysius the Gaul
I can't view the video, but is this talking about the spraying of zinc cadmium sulfate that is discussed in anothe thread in hte chemtrail forum - www.abovetopsecret.com... ?
I don't know why anyone would want to make such obviously false claims - it smacks of deliberate disinfo to scare up a mob!!
And, as always, experiments done in the past are still not actually evidence that somethign is being done now.
So if you can't watch the video, why comment?
What false claims? You didn't watch the video.
It could just as easily be evidence in need of context. Evidence of ramping up in human testing. Are you really so naive as to think we magically grew a conscience despite the ever lasting need for human testing?
Quality poster you are.
Originally posted by YAHUWAH SAVES
They also talk about this spraying from vehicles and I remember months ago someone stated they confronted a man who was spraying from a vehicle and how odd he acted when confronted and how odd the spraying was. I thought perhaps there could have been something to it but the trolls were out in full force on that thread but now I realize it is entirely possible that the spraying from the vehicle was something other than a Bug, Rat or Weed spray as many were forcing there opinion for...
according to Scripture there is nothing Hidden that will not be revealed! All government workers will face an accounting in this life or the next....
Originally posted by zero lift
reply to post by tsurfer2000h
But I disagree with tsurfer2000h about the rest of his post and would encourage him to delve further before being so dismissive of people's concerns - maybe read the NAS report and actual field trial docs, instead of relying on a newspaper re-hash of a NAS Press Release.
The NAS report, just like the later UK Ministry of Defence commissioned report, contains major flaws.
The NAS knew full well that they were'not given access to all scientific results of each trial, which obviously prevented them from be able to make an accurate estimate of dosages for each trial.
They also knew that very little research, if any, had been conducted which investigated adverse health effects to any person (or animal) who had been exposed to Zinc Cadmium sulphide.
Even more importantly, the NAS knew that absolutely no research has been conducted to investigate any adverse health effects experienced by those exposed to Zinc Cadmium sulphide in its BW simulant form - i.e. of a particle size (between 1-5 microns) which was designed to evade the body's natural defences and penetrate the deepest part of the lungs - the alvioli.
In the worst-case scenario, ZnCdS would have the toxic properties of soluble cadmium compounds. However, the physical and chemical properties of ZnCdS are known. It is insoluble in water and lipids and only poorly soluble in strong acids. If it is assumed that in vivo ZnCdS becomes as soluble as any cadmium compound and might release its cadmium ions to react freely with biologic targets, it would be appropriate to estimate the toxicity of ZnCdS from the toxicity of soluble cadmium compounds in general. It is extremely doubtful whether such an assumption is warranted. Our general understanding of metal toxicology gives this worst-case scenario little, if any, plausibility.
In a second scenario, ZnCdS might actually be a biologically inert particle, not more toxic than all the other respirable particles present in our daily environment. This scenario is based on physicochemical properties of ZnCdS (only poorly soluble in strong acids), which results in a lack of acute oral or dermal toxicity. However, the lack of a comprehensive evaluation of the toxicity of ZnCdS, particularly long-term low-level effects, and the fact that ZnCdS might be degraded to some extent, albeit only very slowly, preclude endorsement of such an assumption.
In the third scenario, ZnCdS would have toxic properties similar to those of cadmium sulfide, CdS, an insoluble cadmium compound. ZnCdS has a crystalline structure similar to that of CdS; the only difference is that in ZnCdS, zinc replaces 80% of the cadmium in the lattice. CdS is insoluble in water and lipids and slightly soluble in strong acids. Experimental data on toxicokinetics and toxicity of CdS are available. They clearly show that the cadmium in CdS is much less bioavailable than the cadmium in soluble compounds. ..... Therefore, the subcommittee chose to base its assessment of the potential toxicity of ZnCdS for noncancer health effects on the toxicity of CdS.
Originally posted by zero lift
reply to post by tsurfer2000h
But I disagree with tsurfer2000h about the rest of his post and would encourage him to delve further before being so dismissive of people's concerns - maybe read the NAS report and actual field trial docs, instead of relying on a newspaper re-hash of a NAS Press Release.
Perhaps you should follow your own advice - you can read it for free HERE
The NAS report, just like the later UK Ministry of Defence commissioned report, contains major flaws.
The NAS knew full well that they were'not given access to all scientific results of each trial, which obviously prevented them from be able to make an accurate estimate of dosages for each trial.
Estimates of exposure for each trial are assessed here, and tabulated here
Sampling and analytic methods for determining the concentration of ZCS in target areas is given here, although the text is not properly formatted.
Originally posted by zero lift
The NAS knew full well that they were'not given access to all scientific results of each trial, which obviously prevented them from be able to make an accurate estimate of dosages for each trial.
Er....in your haste to dismiss my post you seem to have missed the point. I said that the NAS, just like the later Ministry of Defence commissioned report, were NOT given access to all trials data. How can you give an accurate estimate for trials of which you hold no data?
Lets see what the NAS actually says shall we?
"THE CONCENTRATIONS OF airborne fluorescent particles of ZnCdS in the Army atmospheric-dispersion studies were measured with impingement and filtration methods. Two of those methods are thoroughly described by Leighton and others (1965), but the methods used at specific locations are not described in detail in Army risk-assessment documents."
This admission concerning lack of vital trials data is very significant. Unfortunately it somehow passed you by.
Let me explain its significance.
In 1962, the UK's Chemical and Biological Warfare research facility at Porton Down, Wiltshire, produced a scientific paper entitled Porton Technical Paper No 811 - Loss of Fluorescence by Airborne Tracer Particles (FP).
One of its conclusions was that ZnCds particles collected by Impactor sampling devices run a great risk of being obscured by local pollution and are not suitable for use in making estimates of particle concentration (and therefore dosage estimates). The US Army used Impactor sampling devices for particle collection in its ZnCds field trials - the Roto-Rod.
Couple that with the fact that the NAS admit that "the methods used at specific locations are not described in detail in Army risk-assessment documents" and one can only conclude that the NAS estimates are somewhat flawed.
In other words, if the Army weren't sure which sampling device was used in which trial, and Porton Down scientists concluded that one of the Armys sampling devices was not capable of providing concentration results, then how is it possible to give an accurate estimate of ZnCds dosage for each trial?
You can't.
Then we have the fact that the NAS based their dosage estimates on particle counts without questioning the purpose of each field trial. This is very important as many of these tests were not done with concentration in mind. Most were purely particle trajectory trials, so the data collection was directed towards that purpose.
Therefore information (particle counts etc) collected during trajectory orientated field trials was useless for use in dosage estimation.
One study reported a loss of as much as 50% of Zn0.8Cd0.2S particles within 2 h of airborne travel in sunlight (Eggleton and Thompson 1961).
Originally posted by Aloysius the Gaul
Originally posted by zero lift
The NAS knew full well that they were'not given access to all scientific results of each trial, which obviously prevented them from be able to make an accurate estimate of dosages for each trial.
You seem to be completley unaware of methods for dealing with data that is known to be less than perfect - I can see why this makes your judgement so poor......
Er....in your haste to dismiss my post you seem to have missed the point. I said that the NAS, just like the later Ministry of Defence commissioned report, were NOT given access to all trials data. How can you give an accurate estimate for trials of which you hold no data?
they did have data - you even say so in this section I quoted - a very bad leap of illogic on yuor part there.
why not? Again you assume that because you think there is a problem with the data therefore it is completely useless.
However there are multiple well known techniques for dealing with deficient data - you can examine what is collected, how it is collected, and what the characteristics of the collection system are, then make allowances, test presumptions and incorporate certainty measurements. Such measures are taught starting in Stats 101
apparently you do not know of any of them......and it is reflected in your unjustified conclusions.
Along with filtration - and apparently the rotorod is well suited to measuer concentrations....oops!!
Originally posted by zero lift
Then we have the fact that the NAS based their dosage estimates on particle counts without questioning the purpose of each field trial. This is very important as many of these tests were not done with concentration in mind. Most were purely particle trajectory trials, so the data collection was directed towards that purpose.
Therefore information (particle counts etc) collected during trajectory orientated field trials was useless for use in dosage estimation.
Says who?
...but since apparently at last 1 of the collection methods is able "to record the same relative changes in airborne particle concentrations" it seems to me that a lot of your basis for complaint is jsut wishful thinking on your part due to ignorance.
And then of course we have the fact that little or no mention was made by the NAS about the deleterious effects of sunlight on ZnCds particles.
And so what?
Your leaps from "the data is not ideal" to "therefore the data is completely useless" are not backed up by any real reasoning.
Originally posted by zero lift
I realise that you appear to have difficulty in understanding this but surely it must be obvious, even to you, that using particle counts obtained from an device that has a proven low collection efficiency for the particle size used in ZnCds experiments cannot give an accurate dosage estimation.
Take a bit of time Aloysius. Do a bit of research on the extensive US/UK/CAN ZnCds field trials programme - examining the actual ZnCds field trials reports would be a start.
You may then realise that the NAS report, just like the UK equivalent, contains major flaws.
Or then again, you may not.