All right. Thank you, ladies and gentlemen. Please be seated. All right. Let the record reflect that we've been rejoined by all the members of our jury panel. Good afternoon, ladies and gentlemen.
THE JURY: Good afternoon.
Frederic Rieders, the witness on the stand at the time of the lunch recess, resumed the stand and testified further as follows:
Frederic Rieders is on the witness stand undergoing direct examination by Mr. Blasier. And good afternoon, doctor.
Doctor, you are reminded, sir, you are still under oath. Mr. Blasier, you may continue with your direct examination.
Dr. Rieders, I think we were talking at the break about environmental conditions with respect to the gate. Let me ask you if--and you described one way that you would do some testing to determine what effect that might have on the amount of EDTA that you started with versus what comes off the stain taken several days or weeks later. Do you recall that?
Confronted with that set of circumstances, to answer the question, mainly how much EDTA might you lose under those environmental--
Did you see any evidence that the FBI did any studies whatsoever to determine what would be the difference in the amount of EDTA in a stain put on a gate with EDTA blood--
--subjected to whatever environmental conditions it was subjected to and then collected from a day to three weeks later?
Now, let me ask you hypothetically about the sock. Did you see any indication in the FBI reports that you were given indicating that any testing was done to determine what, if any, loss you might have in EDTA if you put EDTA blood on the sock at one point in time subjected to changes in temperature, inspection under various different kinds of lighting and multiple handling to determine how much EDTA might be left at the end of all that process?
If you were doing a validation study to determine that question--well, let me ask you this. If you were trying to make some sort of assessment on the quantity of EDTA that you would expect at the end of that process when you do the testing, would you do those kinds of studies to answer those questions?
Did you see anything in the FBI reports indicating whether they did any studies whatsoever to determine whether there might be any oxygen or bacterial degradation of EDTA?
Did you see anything in the FBI paperwork indicating that they looked at the question of what might happen to the amount of EDTA in a stain if an EDTA--some EDTA blood was mixed in with some non-EDTA blood?
Now, you reviewed charts that the FBI produced of their positive controls for EDTA, correct?
The positive controls were made by taking the material, for example, on the swatch or just taking plain blood and adding to it EDTA or taking known EDTA blood and see how it behaves.
Did you see any indication of how long they waited from the time they put the blood on a stain until they actually tested it?
Only if it were to exceed a normal laboratory period; you know, you start something, you continue that day or next day. If it was any length of time, yes.
And if you were trying to simulate what might--what you might expect to find under the conditions which we have with the sock and the back gate, in your opinion, would it be adequate to just take a bloodstain that's dried for a period of an hour let's say and testing it right then?
It does not at all reproduce the conditions of the specimen. So in that rare extent, it does not.
KEY QUOTENow, doctor, the charts produced for the positive controls had relatively large peaks; did they not?
Let me show you what's been marked as 1261. Did you receive a bar chart like that in the material from the FBI?
And let me put that on the elmo. Now, doctor, does this appear to be a bar chart produced in the FBI paperwork? Can you see it?
I'm trying to read the one next to the large numbers. What is it? Yes. I've received that.
And the various different bars indicate EDTA or what matches EDTA found from various samples, correct?
Now, does that particular chart in representing ion counts--let me rephrase this. Did they run positive controls more than just those two times?
Let me ask you one question about the chart before we mark the next set. The two columns on the left indicate dress. Do you see that?
And they indicate approximately the same amounts from a sample called K65 and K65C. Do you agree with that?
No. The one on the right is substantially thicker than the one on the left. No. 2 is substantially thicker than no. 1 as far as the height is concerned.
For the record, 1262-A is discovery no. 4077 and is labeled 50 parts per million EDTA and 40--I'm sorry--1262-B is discovery page 4070, also indicated at 50 parts per million EDTA. And these are both from February 22nd, counsel.
Dr. Rieders, let me show you two charts, 1262-A and 1262-B, and ask you if those appear to be charts testing 50 parts per million EDTA.
One at 9:32 and 25 seconds in the morning and the other one at 1:48 and 11 seconds in the afternoon of the same day.
Now, doctor, could you tell us for chart no. 4077 what was the ion count for 50 parts per million on that particular run?
Now, look at chart 4070, the same standard, the same amount run later that day. What was the ion count later in the day?
And would you agree that, assuming the chart is properly labeled, those two should be the same thing? Well, let me rephrase that. The same thing is being tested in both of those runs?
And do you find it unusual at all that the ion counts would change so much from one test to the next on the same day?
Do you have an opinion on whether ion counts under the conditions of the FBI's experiments can vary that much, as much as is shown in the chart, from run to run in the same day?
Easily, because with the electrospray system, you get numbers that go pretty much all over. So that's consistent with electrospray analysis.
KEY QUOTENow, is this a--if you ran an internal standard with each of those, what--if the equipment is working properly, what would you find?
Well, you'd find that the ratio would be the same if it's the same sample. Mind you, if it's a different sample, it could be, you know, different blood, different thing. But if it's the same sample or the same batch for the analysis, then you would find the ratio is similar, provided everything went all right, even though the numbers are greatly different.
Now, have I asked you to--have you reviewed some material provided by Mr. Martz concerning the amounts of--well, let me rephrase this. Is EDTA appear or allowed to be present in food?
In some of the dried vegetable type things like in peas and beans according to the one FDA release that I have, in pickles, in a variety of foods. I don't recall any what you call basic foods that are eaten in huge amounts like bread or something. But it might be. I don't know.
Have you reviewed the federal requirements in terms of the maximum amounts of EDTA that can be put into various foods?
And have you determined from those materials what you would expect to find in a person's natural blood who is eating materials with EDTA in them?
Doctor, are you called upon to make calculations of how much of a particular substance might be in the bloodstream based on what you ingest by mouth?
And is there a study you reviewed in this case provided by Mr. Martz that talks about the absorption rate of EDTA into the system?
That is a study by Trujillo and--now the second name slips--in the 50's using radioactive labeled EDTA and fed to people.
And what did that study determine was the absorption rate of EDTA into the bloodstream when it was taken by mouth?
319,561.
Easily, because with the electrospray system, you get numbers that go pretty much all over. So that's consistent with electrospray analysis.
It does not at all reproduce the conditions of the specimen. So in that rare extent, it does not.
I think it's one of the artificial fibers that includes EDTA.