Full text: Proceedings, XXth congress (Part 5)

    
  
   
    
   
  
  
  
  
  
  
  
  
   
  
  
  
  
   
   
  
  
   
    
   
    
   
     
   
     
      
   
  
   
   
    
   
     
  
  
  
  
  
  
     
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International Archives of the Photogrammetry, Remote Sensing and Spatial Information Sciences, Vol XXXV, Part B5. Istanbul 2004 
Figure 12. P 
     
Figure 13. Imprint on pig skin 
  
Figure 14. Imprint on human skin 
Using this analysis we are able to determine the coefficients of 
human and pig skin and precisely model the two. The 
characteristics of the imprint or indentations were the same in 
all testing. The mechanics of this can be best described by the 
following. 
For the cycle of indentations from pressure: External pressure 
on the skin causes tissue compression and distortion. If the 
external pressure is greater than the capillary pressure keeping 
the capillaries open, then capillary occlusion occurs. 
Susceptible areas are over boney prominences. 
Occlusion of capillaries leads to the secretion of endogenous 
chemicals that have multiple effects. One is to signal all the 
capillaries in the area to "open up". Another set of chemicals is 
secreted to attract the immune system to send cells to "clean 
up" any damaged tissue. Yet another set of chemicals cause the 
capillaries to become "leaky" to allow the cells attracted to get 
to the tissue affected. 
Initially, the area of capillary occusion will have no blood flow 
and appear white in color. If the circulation is interrupted by 
death, then the area of pressure will never receive any further 
blood flow and remain permanently white. As tissue re- 
expansion requires blood flow, the tissue will remain 
permanently indented. 
If blood flow is restored, blood resumes flowing to an area that 
has capillaries that are "wide open" and "leaky". The net result 
is a red discoloration of the area, and the area begins to swell. 
The swelling follows a pattern similar to the shape of the 
pressure applied; the areas with less pressure will swell first, 
followed by the areas of greater pressure. This will give 
palpable ridges in the area in the shape of the object applying 
the pressure. 
Eventually the tissue recovers, and normal capillary flow is 
restored, again following the pattern of least pressure 
recovering first and most pressure recovering last. 
3.2 Ante and post mortem imprint marks 
This study covered areas of anti and post mortem marks related 
to forensic applications. We all know that when pressure is 
applied to skin, an imprint mark will be made. We also know 
that over a period of time this mark will dissipate and the skin 
will return to normal. There are distinct differences between 
ante and post mortem imprint marks. To model these 
differences we had to model the characteristics at time of 
death. We obviously used pigs for this phase. Figure 15. 
illustrates the procedure. We placed objects on the skin to 
produce indentation or imprints on the pig. À lethal injection is 
made in the heart. Using our targeting and imaging as 
described we monitor the reaction to the imprints in addition to 
imprints made prior to death. The test provided very 
interesting results. 
  
Figure 15. Lethal Injection to the Heart 
The test provided precise method of monitoring the major 
differences between ante and post mortem marks. As stated 
earlier, when pressure is applied to skin, an imprint mark will 
be made. We also know that over a period of time this mark 
will dissipate and the skin will return to normal. It was 
discovered that at the instant of death the dispersion rate of the 
indention stops. It is also noted that the amount of pressure and 
length of time the object that causes the indention does not 
affect the overall depth of the imprint in most cases. This 
opens a new area for forensic study. By modelling the elasticity 
of skin we can calculate the dispersion or lapse rate of the skin 
returning to normal. This can provide the ability to determine 
the time of death after the wound or imprint is made on the 
skin. This observation and characteristics were duplicated in 
subsequent testing. The following Figures 16. and 17. illustrate 
the indentations on the skin. 
  
 
	        
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