This also illustrates some very serious problem when studying these things. The data is of such poor quality, mostly because doctors collect it, that it is hardly usable at all. For example in NZ, if you had any flu like symptoms that year, it was reported as a H1N1 case. Clearly that is not how it works.
Bird flu and SARS where very similar in that 1 perhaps 2 quite young people died and then everyone jumped on the "new disease" bandwagon. A post analisis of the data didn't suggest there was anything out of the ordinary, and some countries did flat out ignore it because they didn't see any support from the data (Austria for example). For example the fatality rate of SARS was suppose to be 3%, but only people sick enough to get admitted to hospital where tested to see if they have it. Many people could have had it with much milder symptoms. BTW i worked directly on some of the SARS data, and well NDA and stuff i can't say much other than its was pretty poor quality.
Make no mistake, we need an organization like WHO (we get a lot of data from them in fact). And we need to have people on the lookout for pandemics. But we need to base these decisions on data, not emotion. Note data may not be serology tests or DNA test. But old fashion symptom progression, disease state and fatality rates with responses to treatments. ie stuff even a 3rd world hospital would have if the doctors would bloody well write down what they thought, did and measured. Something as simple as temperature rather than a blanket statement of "fever".
Of course a bunch of tests/measurements on the general public "background" would also be useful. But this is expensive and hard to do properly since you can't force it on people and you get selection bias and also a bunch of ethics issues.
But a advance lab to create some superbug in some super Crag Venter style is hardly credible. Using evolution to do the dirty work is even less so.
To give you some examples without just a list of reference to papers you probably can't get access too. Common yeast is not the same as lab yeast. Lab yeast does not clump like wild yeast. This is purely unintended selection over the generations with particular lab protocols. Cool eh. We can get some lab strains to replicate quite fast in some media at 37C. Only it turns out that a lot of the "optimal" temperature thing is based again on unintended selection on strains optimized for the most common default lab environments.
We are currently working on tamiflu resistance in evolutionary experiments. Yes we observe resistance in only a few dozen generations. But this already happened in the real world (yea tamiflu more or less never worked properly anyway). We also observe hitchhiking of many things that don't look too good outside the media used. In fact we have to control for the fact that things happen on this media. We let there be a few 100 generations on the media so we don't confuse what is just selection for that media.
And of course all that happened without the presence of a rapidly responding immune system. Now move it into a real host (different media) with a immune system, and you find these lab strains just die out. We see this with lots of different systems by the way.
Bioweapons are even worse than dirty bombs. The threat is not from a terror organization or a stupid scientist. But just old fashion evolution. These make poor bio weapons. But a new pandemic on the scale of Spanish flu would be expensive. However not as devastating as the movies make out. In fact many believe a disaster movie level pandemic is impossible due to the tradeoffs that must be made in the design of the bug/virus.
But don't get me started on these recent H1N1 or bird flu bullshit. I will rant all day.
And why should those environments be even remotely as effective at creating a bioweapon as deliberating creating an environment where the dominant selection processes are for bioweapon potential?
Because evolution just does not work the way you think it does. You can't use evolution to select for a bioweapon, because a bioweapon is not selectively advantageous. Killing your host does not help you perpetuate. Living asymptotically in a host is not a weapon. Getting something that works well in media, has been selected to live well in media and not outside it. We see this all the time. We have math models of it. We have done evolutionary experiments and observed it.
Bioweapons just don't evolve. They must be designed and created. They also don't work well at any rate. Russia and the US didn't agree to stop pursuing them because they thought they could work. They agreed because they had figured out that they just don't work well at all.
Consider how many generations are exposed to these treatments in the real world. Yet we don't see new "bioweapon" strains popping up all the time. And we don't precisely because it really doesn't work that way.
OTOH, it's far easier to cultivate bacteria than viruses. For example, Yersinia pestis, the bacteria that causes bubonic plague can be grown in a modified agar gel [nih.gov] with no need for host cells of any kind. And it's pretty easy to breed in resistance to anti-biotics by exposing the bacteria over many generations to all the anti-biotics in use at doses where a small part of the colony survives.
Working on such data is my day job. It is not even close to as easy as you describe often needing 1000s of generations or more, and you end up with something that is antibiotic resistant *on agar*. Your host is not such a simple media.
Extraordinary evidence demands a better standard than... "you can't dismiss the results, but it may be X Y or Z". The fact that such things (air effects etc) were not taken into account is just plain shoddy experimental work with that level of force. Its up there with youtube videos of free energy machines. Either do your experiment properly or don't make claims that your experiment didn't even test.
Many is vague: let's put a real number on it and say 6 orders of magnitude, or 25 MW. Pretty good size I'd venture. Multiply that by ~40uN/25W and you've got all of 40 Newtons of force. How often do you really suppose a 25MW microwave resonator is operated in a situation where 9lbs of force would be noticeable? Unless I'm drastically overestimating the size of such a thing friction alone would likely hold it in place. And if not a single 1/8" bolt certainly would.
True, i should have run some numbers. In fact 25MW is not far off what accelerators use.
Photon momentum is easy to calculate. E=mc^2 so the mass per second per watt is m=P/c^2, and its moving at the speed of light so multiply by c and you get momentum per second, or force F=P/c . That is for 1N of force you need 3x10^8 watts. Or for one watt 1/3e8=3.333x10^(-9).
Finally, if we take the NASA measurements as indicative of forces being generated...
Lets be very clear, their data shows no such force. Just systematic error. If you get the same "significant" force from the negative control, then its systematic error and you don't make stupid claims.
We understand EM forces and fields very very well. Quite frankly the original claims don't even past a basic "hinky meter" test. They certainly don't have any proper math/physics to back anything up.