Plaintiffs call Dr. Terry Lee, Your Honor. TERRY LEE, was called as a witness on behalf of the Plaintiffs, was duly sworn and testified as follows:
You do solemnly swear that the testimony you may give in the cause now pending before this court shall be the truth, the whole truth, and nothing but the truth, so help you God?
I first took a post doctoral position at Oregon Graduate Center for a period of three years, after which I took a position at Cetus Corporation which is a technology company in the Bay area. And then finally, I ended up at Beckman Research Institute at the City of Hope.
Dr. Frederic Rieders told the jury when he was here that he's testified as an expert witness in excess of 100 times.
I'm a research scientist. I do research and analysis of molecules by liquid chromatography and mass spectrometry.
The City of Hope is -- it's two things: It's a national cancer treatment center, it's also a research institute.
My official title is research scientist. I do studies related to the analysis of biomolecules by mass spectrometry.
One of the processes that is at issue in this case is a cell called HPLC test. Are you familiar with that test?
One of the other tests at issue in this case involves the use of liquid chromatography combined with tandem mass spectrometry using an electrospray interface, what Dr. Rieders referred to as LCESMSMS; are you familiar with that technology?
2403. (The instrument herein referred to as curriculum vitae of Dr. Terry Lee was marked for identification as Plaintiffs' Exhibit No. 2403.)
According to your resume, you've written 129 articles that are listed on the resume. Do any of those articles deal with mass spectrometry of the type that's at issue in this case?
Now, have you reviewed the various tests performed by FBI Agent Martz on certain evidence samples from this case?
I reviewed the analyses that were submitted to the -- to the I.G.'s -- the Court, related to direct analyses of the samples. There was also a set of analyses that were termed validation studies which I believe were not done by Agent Martz but by other people at the FBI. I reviewed Martz's testimony that he gave in the criminal trial. I reviewed Dr. Rieders' testimony that he gave at the criminal trial. I reviewed Dr. Rieders' testimony that he gave in this trial.
Have you been asked to determine from the test results of Agent Martz whether or not the evidence samples tested by Agent Martz could have come from test tubes treated with the chemical EDTA?
Now, one of the tests that Agent Martz performed is a test that he called a negative ion test. What kind of a test is that, sir?
That refers to negative ion mass spectrometry. In mass spectrometry, you have the option of looking at either positive ions or negative ions. In that particular analysis, Agent Martz found no evidence that there was any contamination in the blood samples by EDT
A.
When Agent Martz performed the negative ion test, was he able to see any EDTA at all in the evidence samples?
Now, another test that Agent Martz performed is what we've talked about earlier, this so-called HPLC test, and would you describe briefly what an HPLC test is?
HPLC is -- is short for high pressure or high performance liquid chromatography. It separates mixtures, and the analysis relies upon being able to separate what you want to look for from everything else and assign what is called a retention time to it. The identification is based on the retention time of the compound coming out of the instrument and the UV absorbance signal that the detector monitors.
And reviewed results of other people as well. Is that part of your functions as the head of the mass spectrometry unit at the City of Hope, to review other people's test results?
Now, what do Agent Martz's HPLC tests show as to the possible presence of EDTA from a purple-top test tube in the evidence item?
Finally, Dr. Lee, Agent Martz also performed a so-called positive ion mode test. What kind of test is that, sir?
That's a test exactly like the negative ion test except you're looking at the positive ions instead of the negative ions.
Now, incidentally, Dr. Lee, are you familiar with the equipment that Agent Martz used to perform these tests?
When Agent Martz ran the LCESMSMS test in the positive ion mode to determine whether he could detect the presence of EDTA in the known sample, that is in a sample of blood from a purple-top test tube, was he able to detect EDTA in that testing mode?
Now, when Agent Martz ran the LCESMSMS test in the positive ion mode on the evidence samples in this case, was he able to obtain the same kind of showing as he did when he ran the known samples?
In those tests on the evidence samples, did Agent Martz obtain signals indicating the presence of blood from an EDTA-treated tube in the evidence samples?
Yeah. This is a little bit out of focus up here. Little more. Little more. Little more. Well, trouble is, we want to be able to see the whole thing.
This is a direct comparison of the -- of one of the analyses for the blood which came from a purple-top tube comparing that with analyses of the evidence sample blood.
Okay. Now, this -- this showing that he got from the evidence sample, the small little mole hill of a showing, in your opinion, could that showing be reflecting blood from a purple-top test tube?
The intensity difference is too great. Agent Martz, because he didn't have an internal standard, he designed his experiment such that if there was any errors in the quantitation, that he would err in the right way; in other words, he would always attempt to use more blood from the evidence sample than he would from his positive control. In this case, there's 100 times or more greater intensity from blood obtained from a purple-top tube than he would get from his evidence sample. So that result is inconsistent with the blood from the evidence sample having come from a purple-top tube.
And the procedure that Agent Martz used, is that a standard operating procedure for somebody using these mass spectrometry machines?
Yes, it's a standard operating procedure when you don't have an internal standard that you can do exact quantitation with.
And when Agent Martz did these tests, was there an internal standard commercially available to do these tests?
2404. (The instrument herein described as Chart was marked for identification as Plaintiffs' Exhibit No. 2404.)
(BY MR. LAMBERT) The one we just looked at was for K206 or Q206 this is for Q204. Is this the same type of chart that you just showed us?
So for both of the two evidence samples, socks and back gate, tested by Agent Martz, he got only a trace signal from the evidence sample and some mountainous signal from the known sample?
And once again, Doctor, is it your opinion -- what is your opinion as to whether these little trace signals could have come from a purple-top test tube?
He got essentially equivalent results with his own blood as far as the trace level of EDTA that were detected in his analyses.
So when Agent Martz took out his own blood and tested it in the machine, he got this same little signal from his own blood?
And from a scientific point of view, Dr. Lee, could you tell us what the significance of that is?
The significance, from a scientific point of view, is that since the signal and response are the same, that the likely source of that signal was possibly the same.
Well, Dr. Rieders testified that this wide variation between the small signal shown in the evidence sample and the very large signal shown in the known sample could be the result of some error by Agent Martz in measuring the amount of the evidence sample. Do you believe Dr. Rieders could be correct in that regard?
No, I don't. I think that is extremely unlikely. Blood is a colored substance, so if there was a very large error, in this case it would have to be larger than a -- greater than a ten-fold error, then the solution you were sampling from would have been colored differently. That's a difference that you would not be able to overlook.
So if Dr. Rieders is right, would Agent Martz have to have made the same error every time he ran them?
And I think you mentioned that Agent Martz was intentionally trying to use more of the evidence sample than the known sample. Is that your understanding?
(BY MR. LAMBERT) So he was intentionally trying to use more evidence sample than the known sample; is that your understanding?
That's what would be standard operating procedure for a mass spectrometer doing these tests?
Dr. Rieders also tried to explain the difference between the small signal from the evidence sample and the large signal from the known sample by saying that it was possible that the EDTA in the evidence sample had somehow degraded before these tests were run. Is there any scientific literature that supports Dr. Rieders' opinion that EDTA could degrade so significantly?
EDTA is a very unstable compound; it's not likely to degrade under normal circumstances. And these evidence samples were -- came from different places and were treated differently; yet they all show the same levels. And so it's difficult to imagine the degradation that would be common to all the samples.
And if Dr. Rieders was correct in his degradation theory, how would that explain the results that Agent Martz got in his own blood?
As a scientist, Dr. Lee, what is the most likely explanation for this very small trace that is shown in the evidence sample here in this one test that Agent Martz did?
These results are consistent with a carryover from -- in the instruments. In other words, if you first analyze on the instrument samples which contain a large quantity of EDTA and then you subsequently come in with the samples that don't have any, it's not uncommon to pick up trace levels from various parts of the instruments that have been contaminated with the EDTA and then subsequently alluded off when you did the other analyses.
KEY QUOTEAnd if people are very experienced in doing mass spectrometry, is it something that they are aware of is a problem with the instruments?
My opinion is that it could not have come from those test tubes.
There's 100 times or more greater intensity from blood obtained from a purple-top tube than he would get from his evidence sample. So that result is inconsistent with the blood from the evidence sample having come from a purple-top tube.
None that I'm aware of.
These results are consistent with a carryover from -- in the instruments. In other words, if you first analyze on the instrument samples which contain a large quantity of EDTA and then you subsequently come in with the samples that don't have any, it's not uncommon to pick up trace levels from various parts of the instruments.
This is my first time.