biological evidence i serology
TRANSCRIPT
Introduction to Forensic
Science and Criminalistics
Prepared byPeter Bilous
Eastern Washington University
Chapter 9
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Blood and Physiological Fluid Evidence: Evaluation and Initial Examination
How Biological Evidence Analysis Has Changed Because of DNA Typing
Nature of Blood Collection, Preservation, and Packaging of Biological Evidence Test Controls, Substratum Comparison Specimens, and
Contamination Issues Initial Examination of and for Biological Evidence Forensic Identification of Blood Species Determination Forensic Identification of Body Fluids Forensic Investigation of Sexual Assault Cases Blood and Body Fluid Individuality: Traditional Approaches
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I. How Biological Evidence Analysis has Changed Because of DNA Typing
Prior to the introduction of forensic DNA typing analysis, blood groups were the genetic markers that were analyzed from biological evidence (forensic serology)
Forensic biology now refers to the preliminary examination of biological evidence prior to the DNA typing analysis procedures
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II. Nature of Blood Blood contains cells, nutrients, chemical
messengers, and ingested substances A tube of whole blood will clot producing two
fractions: a yellow serum layer and a dark red clot containing cellular material
Anticoagulants prevent blood clotting yielding a yellow plasma layer and a cell fraction that settles to the bottom of the tube
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II. Nature of Blood
The cellular fraction of blood contains red blood cells (erythrocytes) and white blood cells (leucocytes)
White blood cells are the source of DNA for DNA typing analysis
Red blood cells do not contain any nuclear DNA
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III. Collection, Preservation, and Packaging of Biological Evidence
Blood or Buccal Swabs from Known Person:
Blood is drawn into a vacutainer tube containing an anticoagulant such as EDTA (“purple top” tube)
Buccal (cheek) swabs are often used in place of liquid blood as the known sample
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III. Collection, Preservation, and Packaging of Biological Evidence
Biological Evidence from Scenes: Fresh or web blood should be collected on clean,
sterile, gauze and allowed to dry Four sampling methods for dried blood:
• Cutting – For stains on objects that are difficult to submit to the lab. The cut portion should include unstained areas around the bloodstain
• Swabbing – Stain is transferred to a swab which has been moistened with sterile water or saline.
• Scraping – a sharp instrument is used to scrape the stain off of a surface & onto clean paper
• Elution – using a small amount of saline or distilled water to dissolve the dried stain
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III. Collection, Preservation, and Packaging of Biological Evidence
The most important consideration for preserving biological evidence from scenes is to thoroughly dry the item before packaging and then store in a cool dry environment
Biological evidence must be packaged in paper containers that can breathe
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IV. Test Controls, Substratum Comparison Specimens, and Contamination Issues
1. Known (Exemplar or Reference) Control:• are specimens from a known source• essential for comparison with DNA profiles
from evidentiary specimens
2. Alibi (Alternative) Known Control:• From a known source that may be the source
of the evidence
3. Blank Control:• A specimen known to be free of the item or
substance being tested
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IV. Test Controls, Substratum Comparison Specimens, and Contamination Issues
4. Substratum Comparison Specimens: Substratum refers to the underlying material or
surface on which the evidence is found A substratum comparison specimen is
subjected to the same testing as the evidence The specimen helps to detect interference in
lab tests originating from the evidence surface An unstained portion of the evidence
underlying material is collected for this purpose
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IV. Test Controls, Substratum Comparison Specimens, and Contamination Issues
Evidence may be contaminated in several ways:• Biological material may have been on a surface
before the biological evidence was deposited• During scene searching &/or processing
activities• During laboratory examinations &/or
manipulations
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V. Initial Examination of and for Biological Evidence
The initial examination is designed to evaluate stains for possible evidentiary value
Activities include:• Searching for biological stains• Preliminary tests for physiological fluids• Positive preliminary tests are then subjected to
confirmatory tests• Cutting out or transferring stains to swabs for
subsequent examinations
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VI. Forensic Identification of Blood
Two categories of identification tests: Presumptive or preliminary test
• Used for screening specimens that might contain the substance or material of interest
• Both false positive and false negative results may be obtained
Confirmatory test• Are tests which are entirely specific for the substance or
material for which it is intended• A positive confirmatory test is interpreted as an
unequivocal demonstration that the specimen contains the substance or material
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VI. Forensic Identification of Blood
Presumptive Tests for Blood: Presumptive blood tests are used to screen evidence
for the possible presence of blood Most are color tests and are based on the
peroxidase-like activity of hemoglobin Peroxidase catalyzes the following reaction Reduced Dye + peroxide --> Oxidized dye + water The presence of hemoglobin catalyzes the reaction,
forming a colored dye product Positive presumptive tests do not prove that blood is
present
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VI. Forensic Identification of Blood
Confirmatory Tests for Blood: Older tests included crystal tests such as
the Teichmann and Takayama tests Current immunological tests use
antibodies specific for human hemoglobin, thus combining the confirmatory test for blood with a human species test
The crystal tests and the immunological tests are known as direct confirmatory tests
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VII. Species Determination
Tests must be done on blood specimens to determine the species of origin
Species origin tests are done using immunological methods which involve the interaction of antigens and antibodies
Hemoglobin from human red blood cells can be used as the antigen to produce anti-human hemoglobin serum
Specific antiserum can be used to test for the presence of antigens in unknown specimens
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VII. Species Determination Common immunological species tests include the
Ouchterlony method Extracts of the bloodstain to be analyzed are tested
with specific antisera If the bloodstain contains the antigens
corresponding to the specificity of the antiserum, a visible precipitate (precipitin) is obtained
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VIII. Forensic Identification of Body Fluids
1. Identification of Semen: Semen is a mixture of specialized cells, called
spermatozoa, suspended in a fluid known as seminal plasma
UV light causes semen stains to fluoresce, and is therefore used to locate stains
Both presumptive and confirmatory tests for semen stains are available
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VIII. Forensic Identification of Body Fluids
Presumptive Test for Semen: The AP test is a color test based on the detection of
acid phosphatase, an enzyme from the prostate gland that is found in high concentration in human semen
Confirmatory Test for Semen: A commonly used approach is to use a microscope to
detect spermatozoa in smears made from dried stains When no sperm are found, immunological methods
are used to detect the presence of a prostate gland protein called p30 or PSA
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VIII. Forensic Identification of Body Fluids
2. Identification of Vaginal Secretions, Saliva, and Urine:
There are no reliable methods for identifying human vaginal material
Presumptive tests for saliva are based on the presence of the enzyme amylase
There are no confirmatory tests for saliva Presumptive tests for urine are based on the
presence of urea and creatinine There are no confirmatory tests for urine
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IX. Forensic Investigation of Sexual Assault Cases
1. Coordination of Effort – SANEs and SARTs The medical examination of complainants in sexual
assault cases is performed by specially trained sexual assault nurse examiners (SANE)
Forensic nurses take a lead role in the coordinated response by the sexual assault response team (SART)
Complainants are taken to a medical facilities or a SANE/SART facility to attend to their medical needs and to collect relevant evidence using a sexual assault evidence collection kit (”rape kit”)
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IX. Forensic Investigation of Sexual Assault Cases
2. The Forensic Scientist’s Role: Sexual assault evidence collection kits are
forwarded to the forensic lab for examination The forensic scientist’s primary role is the
analysis of the physical evidence If semen is present it helps to establish the
corpus delicti If semen or other fluids are found, DNA typing is
conducted to determine if there is a match to a suspect or an exclusion
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IX. Forensic Investigation of Sexual Assault Cases
3. Medical Examination: Medical evaluation and treatment of sexual
assault victims initially involves recording the history of the events, tending to any injuries, and documenting any injuries, bruises, or contusions
This is followed by evidence collection, which includes clothing, vaginal swabs, pubic hair combings, any stains on the skin surface, and a known control (blood or buccal swab)
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IX. Forensic Investigation of Sexual Assault Cases
4. Sexual Assault Evidence Collection Kits: Sexual assault evidence collection kits contain a
variety of containers and envelopes plus a detailed set of instructions on how to use them
Not every container/envelope is used in every case
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IX. Forensic Investigation of Sexual Assault Cases
5. Types of Sexual Assault Cases There are three types of sexual assault
cases: unknown offender (identification cases), known offender (consent cases), and sexual assaults involving children
DNA profiling is helpful in identification cases but not in consent cases
State laws define the age of consent, thereby differentiating between an adult and child
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*Figure 9.7*
IX. Forensic Investigation of Sexual Assault Cases
6. Drug Facilitated Sexual Assault: Several drugs are commonly encountered
as “date rape” drugs: rohypnol, GHB, & ketamine
All are depressants with amnestic effects, and are often used along with alcohol
These types of cases require toxicological analysis of the evidence
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*Figure 9.9*
X. Blood and Body Fluid Individuality: Traditional Approaches
1. The Classical or Conventional Genetic Markers:
5 categories of classical genetic markers: blood groups, isoenzymes, plasma (serum) proteins, hemoglobin variants, and HLA
The first blood group markers were ABO, discovered in 1901 by Karl Landsteiner
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*Figure 9.10*
X. Blood and Body Fluid Individuality: Traditional Approaches
ABO markers were first applied to criminal cases involving bloodstains by Dr. Leon Lattes of Italy in 1913
Isoenzymes are enzymes which occur in multiple molecular forms, reflecting differences in the gene that code for the enzyme
Similarly, there are common variants of the protein hemoglobin
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X. Blood and Body Fluid Individuality: Traditional Approaches
2. How Does Typing Genetic Markers Help “Individualize” a Biological Specimen?
A gene is a region of DNA that codes for a particular protein or enzyme
Because chromosomes are paired (maternal and paternal), and there is one gene on each chromosome, the genes are paired
A gene locus is the location on a chromosome where a particular trait is determined
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X. Blood and Body Fluid Individuality: Traditional Approaches
The genes making up a pair at a given locus are called alleles
The alleles may be the same (homozygous) or different (heterozygous)
Population genetics looks at how often alleles found at a given locus occur in a population
A portion of a large population is sampled and tested to determine the frequency of a particular allele
Statistics are used to estimate the frequency of an allele in the entire population