Agent Martz, did you do any testing to see what size blood drop you would get with various quantities of blood?
One of your methods that you used to estimate how much blood you had from the evidence was to look at those blood drops, correct?
No. I used that--basically put them on paper so I would know how much sample to take and I measured a certain amount out so I knew how large the area was.
Does the same amount of blood put on different substrates look different in terms of the quantity, the size of the drops?
Oh, it would depend. Maybe 20, 30 percent. I don't know specifically. I certainly didn't do any calculations.
Did you prepare some sample with blood drops to compare--you indicated you did one set of blood drops on different substrates?
I believe I did something on filter paper and one on a cloth. I think it was a towel.
On a--okay. And did you do a second sample of blood drops on the same kind of material as the towel?
I'm not saying that. I don't know. I didn't measure. I gave you an approximation. I--
So you don't know how much the size of a blood drop will change given different substrates?
No, and that is why, you know, in this particular case when I did the sock I made sure I used the sock as a control and the gate was swabbed with a cotton swab or cotton swatch, so I used the cotton swatch. I used similar material.
How do you know you used the same kind of swatch? You didn't look at them, did you?
Well, they were the type that were used for serology and DNA and I got mine from the DNA unit.
In your opinion can the size of a blood drop with a given quantity of blood vary by eight times, depending on the substrate?
Did you examine the sizes of blood spots that you had in your photograph to determine whether or not what the difference might be with different substrates with the same amount of blood?
It is for the use--purpose of refreshing recollection. It is also a speaking objection. Have a seat.
I would like to make a correction. This is something I did prepare here. I thought you were referring to the other one.
Agent Martz, when you prepared these did you measure out the quantities of blood that you put on them?
1274. Those are all labeled five microliters, so I know that that is what I did. In this other one, 1275, I don't remember what I did.
Do you remember me showing you that picture about a hour and a half ago and asking you how much blood you used for that second picture?
I can't remember if that is what I said. It--I probably said five--I don't know if I said ten, five. I don't know what it is.
Let me ask you a foundational question. 1275, the second picture, was that the same substrate as the first?
When you did the experiment, this dilution experiment, did you write down any of the conditions of your experiment?
I felt for the purposes that I did there was no reason to do it. The pictures are quite evident. I did it for dramatic effect just so you could see the pictures.
KEY QUOTENo. I--the amount of blood makes absolutely no difference. It is the dilution factor that is important.
KEY QUOTEAgent Martz, looking at 1274, those are five-microliter blood drops that you put on some sort of substrate, two different substrates, correct?
And this was what you used to determine what a five-microliter blood drop--or five microliters of blood would look like?
So you have no idea what five microliters of blood would look like on a swatch from LAPD, do you?
And you are using quantities of blood in this experiment from the evidence that were relatively close to the minimum detectable amounts that you had determined for your negative ion test, correct?
The 207, I don't know. As I told you, I don't know where it came from. You showed me a picture. I don't know where it came from.
I tried to take the same amounts of cuttings from both. I tried to get the same amount of blood.
It is all relevant--relative. I didn't use as much as I was presented. There is more present now--there is less present now than there was when I started.
So you didn't use all of Q207 to try to get as much blood as possible so that you could have higher amounts of blood to look for EDTA, did you?
You did not use all of Q207 which had much more blood than the cutting you took, correct?
In all cases I took larger than the minimum amount that was needed and I combined 206 and 207.
And you had determined the minimum amount you needed from your calculations of sizes of blood drops and what size square swatch you would need to have minimum amounts of blood, correct?
Did you suspect, when you saw the 160 ion in the back gate and the sock, that there might be EDTA there?
KEY QUOTEYou could have used more blood than you used in that experiment to try and find the 132 daughter ion, couldn't you?
You could have used more blood, couldn't you, if you wanted to use a larger quantity of blood to try and find whether there was a true EDTA spectrum there, couldn't you?
To me it was irrelevant and I didn't want to consume all the evidence in case the Defense wanted to use it.
You asked--you said you called the Prosecution to see if you could get some more, didn't you?
Did you ever ask for some more so that you could run larger quantities of blood to really determine whether there was EDTA there or not?
You didn't make any effort to try and run more blood than you had run in your first set of tests to try and actually identify EDTA in the back gate and the sock, did you?
Well, I did, and that is why I went to the positive ion mode the next day, because I felt that EDTA may be present in blood.
Quantity, Agent Martz. Did you ever try to test more blood that you had available to you when you suspect there was EDTA on the gate and the sock?
I felt there was a better way and that was to do the positive ion and that is the way I looked for the EDTA. It was ten times more sensitive.
You weren't concerned with using up what you had available on the sock, were you?
I didn't know what all their testing needed to be done. If DNA testing needed to be done, there would be more blood needed. If it was just for EDTA--there is more things to be done than EDTA.
Did you ever ask, "Can I take another cutting since we are pretty close to minimum detectable limits"?
No, because we weren't concerned with that because minimum detectable limit had nothing to do with whether it was preserved or non-preserved blood. In preserved blood there was so much present it didn't make any difference.
If you test around minimum detectable amounts you are going to find less, aren't you, if it is there? A lot less, aren't you?
I don't know about a lot less. Every instrument has a minimum detectable limit and you either have it or you don't have it and the sock and the gate didn't have it.
Did you ever consider trying to test your suspicion that you founded EDTA by testing a larger quantity of blood?
I felt for the purposes that I did there was no reason to do it. The pictures are quite evident. I did it for dramatic effect just so you could see the pictures.
Did you suspect, when you saw the 160 ion in the back gate and the sock, that there might be EDTA there? Yeah, yes.
No. I--the amount of blood makes absolutely no difference. It is the dilution factor that is important.
I always try to save evidence in case the Defense wants to examine it.