Thanks ros and Timber. I opened the thread this AM and my jaw dropped at RL's inane logic. I can give RL a kind of quick analogy. We can deduce a living animals age by counting rings on the animals scales. SO, why dont we count scales on a ,mammal? We should be able to falsify the data by counting scales on a deer perhaps.
C14 is not used where the ages of the substance or sample are already known ,(especially with a technique that has a physical quantitation limit like the 30-50K year limit I previously mentioned)
Why arent the CReationists , who are eager to disprove the ancient ages of Cretaceous samples also doing C14 to do exactly what you state? Perhaps they arent that stupid either.
A minor, but important reason for NOT doing C14 is sample size and the need to do destructive testing on a number o samples that could destroy the fossil . Fossils need to have some sort of carbon that is in equilibrium with the entire sample(and the carbon 14 is already at an initial equilibrium of 1/1800+/- with C12 and C13). BUUUT, in most cases, the fossil has been turned to silica and not limestone (limestone can contain Carbon in the Calcium carbonate structure, thats why we can do C14 on recent cave deposits) and theres not a whole lot of carbon in the silicate sample(like mostly NONE). As far as the " Hell Creek soft tissue" (which weve discovered wasnt really so soft, because it had to be etched out of the crystalline matrix). the amount of actual carbon is lower than originally believed. The flouroapatite content was primary and the carbon would have been scattered throughout the crystal matrix, thus probably requiring a lot of destructive sampling of a lot more than needed. So we , perhaps, may have had to destroy a sample to acquire information by a dubious method that is of no scientific use after all.
As you seem to want to do,We dont have to continually provide "proof of concept" for various isotope techniques. We know that they work and we know their limitations. So, to sample and test something that is way beyond the functional limit of the method is just plain stupid (i do nt wanna keep harping on this and using the word stupid but its the only descriptor that adequately fits). Its like trying to do mineral analyses to a part per billion level using a wet chemistry assay kit. (Course I like ros's suggetion of playing of a millstone to see whether its not really a"paleo- CD")
When we are way below a limit of quantitation by virtue of the testing procedure. (like we can tell how much iron is in an ore by creating a blue color liquid that we can analyze with transmission spectroscopy method-and it workd down to the high ppm level) . However, if we are looking for a ppb level, we have to give up our "colorometric" method and trust electronic instruments where "detectors" are used to find the iron in solution at really low levels. We give up our eyes and trust electronics.
I imagine that, had you a chance to remove that silly above post, you would, and I shall say no more unless you keep bringing it up. You really ought to learn something about the validity and economics of isotope testing. Its not a technique that we go aimlessly waving around because there is much to understand about whether the sample itself is even datable because of contamination, or whether any zircons in the matrix are actually transported via sediment transfer. etc etc. Couple that with the fact that, depending on the cleanup , C14 can be anywhere from 1500 to 3500 per sample and we always take multiples.
Unscrupulous (or Creationists "for profit" labs would love doing your samples) Course yer science would be in question if you kept coming up with any data from the Cretaceous.
It was worth a laugh though.
OH yeah, Your skills at "quote mining" are getting quite professional, if ros didnt post the whole paragraph that you eviscerated, you maybe coulda had some "quote mine credibility"