Agent Martz, you testified yesterday that you had no bias one way or the other either for the Prosecution or for the Defense. Do you remember that?
Now, yesterday morning do you recall my asking you questions and you answering the questions before the break?
And by the way, during Dr. Rieders' testimony you were consulting with the Prosecutors throughout the course of that examination, were you not?
And you were providing them with--Miss Clark with instructions as to what questions she might raise and what technological issues she might raise?
During each break were you down there conferring with the Prosecutors in this case while Dr. Rieders was testifying?
I don't know about each break. I did confer with them when they asked questions, yes.
And you were conferring with them during the course of my questioning of Dr. Rieders, correct?
And you decided after the break that you needed to be much more of an advocate, didn't you?
I think I decided that I had to be more truthful. I was not telling the whole truth with yes and no answers.
KEY QUOTEYou indicated that the only other time you testified in this case for the Defense is where two police officers were charged with murdering a civilian?
I won't say that is the only time. That is the time I remember. That is the only one I remember.
During the course of your 17 years experience with the FBI, you have never testified for the Defense other than that and other than yesterday and today?
When I met with you in Washington about two weeks ago did you have a conversation with the Prosecutors after that meeting?
I'm sure that I talked to them somewhat about it. I don't remember the specifics of what I told them.
I can't even remember the specifics of what we talked about, you know, all the specifics. I did talk to them after our meeting.
Did you talk to them about some of the issues that you thought I was going to raise and how you might confront them?
I may have mentioned something, but I was confused. As I told you when you came to Washington, I didn't know why you were calling me to testify.
Now, can you tell me one time in your 17 years where after you talked to the Prosecutors about a case that you worked on that you called the Defense to talk to them and explain the issues to them?
Can you tell me one time in your 17 years experience when you met with the Prosecutors about a case that you followed that up by conferring with the Defense to tell them what you discussed?
I've had occasions where I've talked to the Defense after I've talked to the Prosecution.
Do you make that a practice of letting the Defense know when you have conferred with the Prosecution about test results?
Do you make it a practice to let Defense counsel know what issues they might want to raise with you or with other experts?
Now, you were asked a lot of questions about whether Dr. Rieders could have performed some of the tests that I was asking you about yesterday to validate what you might expect to lose by way of EDTA given environmental conditions. Do you remember that?
Is it your understanding--whose responsibility--when you design a test like this, whose responsibility is to it validate it?
The test validates itself basically. You run standards and controls. In chemical analysis the instrumentation is all established. It has been validated. And in a chemical analysis that we do in the laboratory, we identify unknown chemicals on a daily basis and the instrumentation has all been established and the identification of a chemical has been established based on its mass spectrum and we routinely do that and that is what I did in this case. The validation is just to show that the chemical you are looking for can be extracted. The identification is based on mass spectrum which is well-established, but in order to get to the mass spectrum you have to extract it what so you have to do is show by using a control that you can extract that chemical and identify it.
Well, I think I can't remember when I testified the other day, but I work certainly more than a day and probably less than a week in developing a procedure that would extract the EDTA out of blood.
And that validation concerned just determining whether taking blood from an EDTA tube, putting it on a swatch and then letting it dry for an hour and testing it, whether you could detect EDTA, correct?
You didn't do any validation study whatsoever to determine what sample preserved under the way these samples were preserved, collected, environmental factors, you did no validation study whatsoever to determine what if any loss you might have in EDTA, did you?
In this particular case I didn't believe it was necessary. What I had was the best scenario. I had--
Now, when I met with you in Washington I had requested your digital data, hadn't I?
Now, you mentioned yesterday you were talking about the 1954 study and you felt that there were some problems with that?
One of the things you mentioned was that they found thirty parts per million EDTA in the bloodstream at some point?
Under what conditions did they find thirty parts per million EDTA in someone's bloodstream?
Do you have any reason to believe that Mr. Simpson or Miss Nicole Brown Simpson had injected EDTA at any time on June 12th?
Now, you referred to that study for the purposes of explaining that they found thirty parts per million, correct?
But you are not prepared to accept the fact that the study found only five percent of EDTA taken by mouth gets into the blood?
And do you accept the fact that that cite is in a textbook that is used in every medical school, that five percent of what you ingest gets into the blood?
Based on all the research that I did, all the latest literature refers back to the study.
When you read that particular study, did you have any--did you--did you recognize it, that it was a study in pharmacokinetics?
Well, I was looking at the paper because it was the study of EDTA. That was my interest in reviewing the paper.
I didn't criticize the paper. The paper criticized itself and I was just bringing that up.
Let me show you Defense 1268. That is the last page of that document that you are saying has contrary data to the absorption rate?
Tell me where in that paragraph says that there is contrary information about absorption rate?
It says: "The low absorption after oral administration is very surprising in view of the finding that the material is affected by the"--I'm having trouble. Can you focus that?
"Is affected by the route in accelerating the excretion of yttrium and lead. There is no satisfactorily readily apparent explanation at this present"--
Well, it says, the low absorption of an oral administration is very surprising because in another paper they were able to remove yttrium and lead and to remove that you have to get into the bloodstream.
But it is your interpretation of that document that that says there is a different absorption rate than five percent?
It applies a different absorption rate because to effectively remove a chemical from the blood you have to get into the blood.
Now, you indicated yesterday, when Miss Clark was asking you about possible explanations for what you found that is consistent with EDTA on the back gate and the sock, you mentioned an artifact due to the matrix effect. Do you remember that?
So you tried to check that hypothesis and you weren't able to check it out, correct?
It is a possible explanation. We have several explanations that I mentioned. That is a possible one.
I don't think it is likely. I talked to some other experts that thought it was likely.
Agent Martz, let me show you Prosecution 544-E. Incidentally, yesterday in the morning, before the break you testified that what you saw on the back gate and on the sock was consistent with EDTA, correct?
No, I didn't say that. I said one of the charts had an ion that was consistent, or if I didn't, that is what I meant to say.
Well, you set up the experiment. This is the evidence from the back gate, is it not?
There is an ion there and that is the same ion you would get with EDTA there and the parent ion is there, isn't it?
And the retention time is consistent even though, as you stated, your chromatography was not particularly definitive?
Now, the exhibit that we have on the elmo now is the gate chart, correct, when you were looking for the 160 ion, right, at the bottom?
No. As you mentioned with the camera with Dr. Rieders, if you are looking at one specific ion, it is easier to see, but if you are doing a full scan you may not see all the ions, but for me to identify it it has to be present.
KEY QUOTEAre you saying the 160 is not present in the full daughter spectrum of the same sample?
And if you had really been looking for the 132 ion, you could have done the same kind of scan you did for the 160, couldn't you have?
No, it wasn't that I didn't want to find the 132 ion. I needed the full daughter spectrum. In finding the 132 ion, it would just be like finding the 160 ion by itself. It could be a screening test. In order to confirm I need all the ions together in a certain ratio.
KEY QUOTEYou said yesterday that you would have loved to have an internal standard, correct?
That would have made your test from a non-quantitative test to at least some measure of quantitation, correct?
Agent Martz, you testified that this was not designed to be a quantitative test, didn't you?
Now, you are aware now, aren't you, that there is an internal standard that is commercially available that you could have used?
Well, you showed me a book yesterday. I still haven't called the manufacturer to confirm that it is available, but did you do that? Is it available?
I looked at a very close--I didn't look at it very closely, but I saw something that you showed me that you said it was EDTA.
Agent Martz, let me show you--perhaps we could have a copy of this page as well as the cover marked as the next exhibit.
Agent Marks, let me show you from the bottom of page 49 of that catalogue, does that appear to be an internal standard available that you could have used with your testing?
Was it a gram? I can't remember. A gram. I could have bought the smaller standard, yes.
All right. Mrs. Robertson, would you have Mr. Lee make a copy for us, please. Mr. Blasier.
Now, you were shown quite a few charts by the Prosecution, the red bar charts, correct?
Let me show you 552. Agent Martz, you prepared this, as well as several other charts, in an attempt to compare quantities by ion count, did you not?
It was prepared to show the dramatic difference between preserved and non-preserved blood.
Now, you have indicated that your ion counts can fluctuate because of the vagaries of the instrument by four-fold, can't they?
So you could adjust those either to you make them four times bigger or four times smaller and that would still be within the realm of the tolerance of your machine? Fair enough?
Well, that is a big variance. You generally don't get that large, but I would agree that that day it was four-fold.
I think I decided that I had to be more truthful. I was not telling the whole truth with yes and no answers.
It had long since been destroyed, hadn't it? Yes, it had.
No. As you mentioned with the camera with Dr. Rieders, if you are looking at one specific ion, it is easier to see, but if you are doing a full scan you may not see all the ions, but for me to identify it it has to be present.
Yes, it does.
No, it wasn't that I didn't want to find the 132 ion. I needed the full daughter spectrum.