TRACE
EVIDENCE
BLOOD
GROUP
DR ZUBAYER AL
MAHMOOD
Forensic science > Forensic science laboratory :
Forensic science > Forensic science laboratory :
Forensic science is the study & application of different
scientific knowledge to the process of law involving the
scientific examination & evaluation of evidences.
Major divisions of Forensic science laboratory
1.Physical & chemical instrument division
2.Biology division
3.Serology division
4.Toxicology division
5.Chemistry division
6.Documents examination division
7.Photography division
8.Lie detection division
9.Museum
Trace evidence
Trace evidence :
Any trace substance which could be found in the scene of
crime with assailant or victim of the crime that has
evidential value to link or investigate crime is trace
evidence.
Ex: Semen, hair, bloodstain
Locard’s Principle of Exchange
Locard’s Principle of Exchange (Lawyer & doctor
Edmond Locard, 1877-1966): It states that when any two
objects come into contact, there is always a transference
of material from each other. In other words, when an act
of crime is committed there must be sign of crime both
in the accused & the victim.
Some important trace evidences
Some important trace evidences -Blood stain, seminal
stain, hair, Saliva stains, vaginal fluid, fecal stains, vomits
stains, urine, skin, tooth pulp, nails & dandruff, nail mark,
bite mark etc.
Seminal stain as trace evidence
Semen : It is grayish yellow, thick, jelly like alkaline fluid
with characteristic order, consists of spermatozoa,
epithelial & other cells suspended in a fluid known as
seminal plasma.
Quantity: 2-5 ml/ejaculation
Sperm count: 200-500million/ejaculation.
100million/ml,
200-500 reach to the ampulla, 90% motile
at
ejaculation.
Circumstances in relation to semen examination
1.Rape or attempted rape
2.Lust murder
3.Unnatural sexual offences
4.Disputed paternity
5.Legitimacy
6.Sterility
7.Divorce case
8.Artificial insemination
Materials may me stained with semen-
1.Clothes
2.On person
3.Bedclothes
4.Seats of a
motorcar
4.The floor
of grass at
the scene of
crime.
Collection of materials
1.Dried or drying seminal stain on the perineum or thighs
is collected with damp swab.
2.Stain from the vagina is collected with a pipette/throat
swab/vaginal washing
3.A portion of fabric containing seminal stain is cut
out, dried & preserved.
4.The pubic hair with seminal stain should be plucked &
placed in a container.
5.Seminal stain on a smooth & impervious surface should
be gently scraped with the point of a knife into a
glass container.
Examination of seminal stains
1.Physical
2.Chemical
3.Enzymatic
4.Microscopic
Tests for semen
1.Florence test
2.Barbario’s test
3.Acid
phosphatase
test
4.Creatine
phosphokinas
e test
5.Ammonium
Molybdate
test
Hair as trace evidence
May answer many questions of medico legal importance
–
1.Is it hair or not –Cuticle, cortex, medulla
2.Human or animal
3.Male of female
4.From what part of the body
5.Age of the person
6.Identical with that of victim or suspect
7.Naturally forcefully removed
8.Detection of poison
9.Identification of weapon
10.Peculiarity of hair
11.Sexual offence & hair
12.Time since death
Difference between human hair & animal hair
Points Human hair
1.Fine & thin
Animal hair
1.Coarse & thick
1.General
character
2.Cuticle
3.Cortex
4.Medulla
5.Pigment
6.Shaft
diameter
7.
Precipitin
test
2.Cuticular scales are soft,
thin & flattened
3. Well striated, 4-10 time
as broad as medulla
4.Thiner, even may be
absent.
5. More towards the
periphery of the cortex
6.Usually 50-150µm
7.Specific for human
being.
2. Cuticular scales are
very marked with large &
step like or wavy
projections.
3. Thin, rarely more than
twice as broad as medulla.
4.Wider
5. It may be central,
peripheral or uniform.
6.Either <25 or>3000
µm.
7.Specific for animal
Blood stains as trace evidence
Medico legal importance of blood:
Civil:
6.Diputed parenthood
7.Divorce & nullity of marriage
8.Compensation case
9.Medical negligence
Blood stains as trace evidence
Criminal
1.Identification of the victim or offender of a crime –
homicide, sexual offences etc.
2.The cause of death –detection of poison, pathology
3.Time of death –different chemical & biochemical
tests
4.Time of crime/injury
5.Criminal abortion
6.The malingering case
DD of bloodstains
1.Rust stain or mineral stain
2.Vegetable stain –bleached with chlorine water
3.Synthetic dry stain –react with HNO3
4.Stain of grease, tar or pitch –dissolve in alcohol,
chloroform, ether
Variety of bloodstains
1.Drop
2.Splashes or exclamation
mark 3.Pools
4.Spurts or squirt
5.Smear
6.Trails
Questions of MLI in relation to blood &
blood stain
1.Blood or not
2.Human blood or animal blood
3.Source of blood –single/multiple, victim/assailant,
arterial/venous/menstrual/vomited/haemoptysis/abortus/pat
hologial
4.Antemortem or postmortem
5.Time of death
6.Age of the person
7.Sex of the person
8.Blood group of the person
9.Time of bleeding
10.DNA profiling
Examination of blood/blood stains
1.Physical examination
2.Microscopic examination
3.Spectroscopic examination
4.Chemical examination
5.Sero-immunological tests
Tests for of blood/blood stains
1.Spectroscopic examination detects –Oxyhaemoglobin,
reduced haemoglobin, carboxy-haemoglobin,
methaemoglobin, acid hemin, haemocromogen
2. Chemical tests –
A.Benzedine
test
B.Phenophthalin test (Kastle Meyer test)
C.Leucomalachite green test
D.Orthotolidine test (Khon & O’kelly test)
E.Luminal test
Tests for of blood/blood stains
3.Microchemical tests/Crystal tests/Tests for haemoglobin of
blood (Confirmatory tests)
A.Haemocromogen crystal test (Takayama
test) B.Haemin crystal test (Teichmann’s test)
4.Sero-immunological tests
A.Ring test
B.Antiglobulin consumption test
C.Mixed antiglobulin test
D.Diffusion precipitaion in gel
E.Passive haemagglutination test
F.Gel electrophoresis test
G.Precipitin test
Difference between ante mortem and post mortem clot
Point Ante mortem clot Post mortem clot
1.Consistency More firm & friable. Rubbery & gelatinous.
2.Composition Composed of mainly of
platelets & fibrin or
aggregated platelet
producing fibrin strands
entangling the blood cells.
Lack of fibrin strands.
3.Attachment to the
underlying vessel wall
Almost always has a point
of attachment.
Lacks attachment to the
underlying vessel wall.
4.Lines of Zahn May be present Absent
5.Dryness Dry Moist
6.Site of formation In the living circulation Clotting after death and also
in extravascular
accumulations of blood.
Difference between fresh & menstrual blood
Point Fresh blood Menstrual blood
1. Clot formation Occurs Not occurs
2.Colour Bright red Dark red
3.Odour Salty odour Fishy odour
4.Viscosity Less viscid More viscid
5.Reaction Alkaline Acidic
6.Presence of
endometrial and vaginal
epithelial cell
Absent Present
7.Presence of
micro organism
Absent (except disease) Lactobacilli,
Trichomonas vaginalis,
Candida albicans etc are
present.
Difference between male & female blood
Traits Male blood Female blood
1. Sex chromatin in
leukocytes
44+XY 44+XX
2. Davidson’s
body in neutrophil
Absent Present in upto 69%
neutrophils of
females
Blood group
• Red cell membranes have antigens on their external
surfaces
• These antigens are
– unique to the individual
– recognized as foreign if transfused into another
individual
– promote agglutination of red cells if combine with
antibody
– more than 30 such antigen systems discovered
• Presence or absence of these antigens is used to classify
blood groups
• Major blood groups – ABO & Rh
Genotype & Phenotype
ABO system
AA.–A
AB.–
B OO –
O AB –
AB
MN
System
AM. –M
AN.–
N MN –
MN
Rh Factors
Rh+ve
Rh-ve
ABO Blood Groups
• Most well known & clinically important blood group
system.
• Discovered by Karl Landsteiner in 1900
• It was the first to be identified and is the most
significant for transfusion practice
• ABO blood group consist of
o two antigens (A & B) on the surface of the RBCs
o two antibodies in the plasma (anti-A & anti-B)
Reciprocal relationship between ABO antigens and
antibodies
ABO antigens & corresponding antibodies
Inheritance of ABO Blood Groups
• Follows Mendelian principles
• Blood group antigens are “codominant”- if the gene is
inherited, it will be expressed.
• There are three allelic genes -A, B & O
• Some aberrant genotypes do occur but they are very
rare.
• Understanding of basic inheritance important.
Inheritance of ABO Blood Groups
• Two genes inherited, one from each parent.
• Individual who is A or B may be homozygous
or heterozygous for the antigen.
o Heterozygous: AO or BO
o Homozygous: AA or BB
• Phenotype is the actual expression of the genotype,
ie, group A
• Genotype are the actual inherited genes which can
only be determined by family studies, ie, AO.
Example of Determining Genotype
• Mother’s phenotype is group A, genotype
AO
• Father’s phenotype is group B, genotype BO
Other Examples
Rh typing
• Normal typing for Rh antigens only includes
typing for Rh (D).
• The result of this typing determines the Rh status
of the cells (Rh - positive or Rh - negative).
• Some Rh typing sera is diluted in high protein
solutions and may require a negative control.
• It is recommended to use two monoclonal anti-D
sera from two different manufacturers labeled as
D1 and D2, especially to confirm all Rh negatives
Various antigens in Rh system
Rh+ve & Rh-ve blood type
Genotype Blood type
(+,-) or (+,+) Rh+
( - ,-) Rh-
Importance of blood grouping
1.Disputed paternity
2.Disputed maternity
3.Source of blood
4.Stains due to body fluid
5.Identity
6.Cause of death
7.Miscarriage
8.Assist in matching in
disaeter.
Thanks to all

traceevidencebloodgroup-180409190814.pptx

  • 1.
  • 2.
    Forensic science >Forensic science laboratory : Forensic science > Forensic science laboratory : Forensic science is the study & application of different scientific knowledge to the process of law involving the scientific examination & evaluation of evidences.
  • 3.
    Major divisions ofForensic science laboratory 1.Physical & chemical instrument division 2.Biology division 3.Serology division 4.Toxicology division 5.Chemistry division 6.Documents examination division 7.Photography division 8.Lie detection division 9.Museum
  • 4.
    Trace evidence Trace evidence: Any trace substance which could be found in the scene of crime with assailant or victim of the crime that has evidential value to link or investigate crime is trace evidence. Ex: Semen, hair, bloodstain
  • 5.
    Locard’s Principle ofExchange Locard’s Principle of Exchange (Lawyer & doctor Edmond Locard, 1877-1966): It states that when any two objects come into contact, there is always a transference of material from each other. In other words, when an act of crime is committed there must be sign of crime both in the accused & the victim.
  • 6.
    Some important traceevidences Some important trace evidences -Blood stain, seminal stain, hair, Saliva stains, vaginal fluid, fecal stains, vomits stains, urine, skin, tooth pulp, nails & dandruff, nail mark, bite mark etc.
  • 7.
    Seminal stain astrace evidence Semen : It is grayish yellow, thick, jelly like alkaline fluid with characteristic order, consists of spermatozoa, epithelial & other cells suspended in a fluid known as seminal plasma. Quantity: 2-5 ml/ejaculation Sperm count: 200-500million/ejaculation. 100million/ml, 200-500 reach to the ampulla, 90% motile at ejaculation.
  • 8.
    Circumstances in relationto semen examination 1.Rape or attempted rape 2.Lust murder 3.Unnatural sexual offences 4.Disputed paternity 5.Legitimacy 6.Sterility 7.Divorce case 8.Artificial insemination
  • 9.
    Materials may mestained with semen- 1.Clothes 2.On person 3.Bedclothes 4.Seats of a motorcar 4.The floor of grass at the scene of crime.
  • 10.
    Collection of materials 1.Driedor drying seminal stain on the perineum or thighs is collected with damp swab. 2.Stain from the vagina is collected with a pipette/throat swab/vaginal washing 3.A portion of fabric containing seminal stain is cut out, dried & preserved. 4.The pubic hair with seminal stain should be plucked & placed in a container. 5.Seminal stain on a smooth & impervious surface should be gently scraped with the point of a knife into a glass container.
  • 11.
    Examination of seminalstains 1.Physical 2.Chemical 3.Enzymatic 4.Microscopic
  • 12.
    Tests for semen 1.Florencetest 2.Barbario’s test 3.Acid phosphatase test 4.Creatine phosphokinas e test 5.Ammonium Molybdate test
  • 13.
    Hair as traceevidence May answer many questions of medico legal importance – 1.Is it hair or not –Cuticle, cortex, medulla 2.Human or animal 3.Male of female 4.From what part of the body 5.Age of the person 6.Identical with that of victim or suspect 7.Naturally forcefully removed 8.Detection of poison 9.Identification of weapon 10.Peculiarity of hair 11.Sexual offence & hair 12.Time since death
  • 14.
    Difference between humanhair & animal hair Points Human hair 1.Fine & thin Animal hair 1.Coarse & thick 1.General character 2.Cuticle 3.Cortex 4.Medulla 5.Pigment 6.Shaft diameter 7. Precipitin test 2.Cuticular scales are soft, thin & flattened 3. Well striated, 4-10 time as broad as medulla 4.Thiner, even may be absent. 5. More towards the periphery of the cortex 6.Usually 50-150µm 7.Specific for human being. 2. Cuticular scales are very marked with large & step like or wavy projections. 3. Thin, rarely more than twice as broad as medulla. 4.Wider 5. It may be central, peripheral or uniform. 6.Either <25 or>3000 µm. 7.Specific for animal
  • 15.
    Blood stains astrace evidence Medico legal importance of blood: Civil: 6.Diputed parenthood 7.Divorce & nullity of marriage 8.Compensation case 9.Medical negligence
  • 16.
    Blood stains astrace evidence Criminal 1.Identification of the victim or offender of a crime – homicide, sexual offences etc. 2.The cause of death –detection of poison, pathology 3.Time of death –different chemical & biochemical tests 4.Time of crime/injury 5.Criminal abortion 6.The malingering case
  • 17.
    DD of bloodstains 1.Ruststain or mineral stain 2.Vegetable stain –bleached with chlorine water 3.Synthetic dry stain –react with HNO3 4.Stain of grease, tar or pitch –dissolve in alcohol, chloroform, ether
  • 18.
    Variety of bloodstains 1.Drop 2.Splashesor exclamation mark 3.Pools 4.Spurts or squirt 5.Smear 6.Trails
  • 19.
    Questions of MLIin relation to blood & blood stain 1.Blood or not 2.Human blood or animal blood 3.Source of blood –single/multiple, victim/assailant, arterial/venous/menstrual/vomited/haemoptysis/abortus/pat hologial 4.Antemortem or postmortem 5.Time of death 6.Age of the person 7.Sex of the person 8.Blood group of the person 9.Time of bleeding 10.DNA profiling
  • 20.
    Examination of blood/bloodstains 1.Physical examination 2.Microscopic examination 3.Spectroscopic examination 4.Chemical examination 5.Sero-immunological tests
  • 21.
    Tests for ofblood/blood stains 1.Spectroscopic examination detects –Oxyhaemoglobin, reduced haemoglobin, carboxy-haemoglobin, methaemoglobin, acid hemin, haemocromogen 2. Chemical tests – A.Benzedine test B.Phenophthalin test (Kastle Meyer test) C.Leucomalachite green test D.Orthotolidine test (Khon & O’kelly test) E.Luminal test
  • 22.
    Tests for ofblood/blood stains 3.Microchemical tests/Crystal tests/Tests for haemoglobin of blood (Confirmatory tests) A.Haemocromogen crystal test (Takayama test) B.Haemin crystal test (Teichmann’s test) 4.Sero-immunological tests A.Ring test B.Antiglobulin consumption test C.Mixed antiglobulin test D.Diffusion precipitaion in gel E.Passive haemagglutination test F.Gel electrophoresis test G.Precipitin test
  • 23.
    Difference between antemortem and post mortem clot Point Ante mortem clot Post mortem clot 1.Consistency More firm & friable. Rubbery & gelatinous. 2.Composition Composed of mainly of platelets & fibrin or aggregated platelet producing fibrin strands entangling the blood cells. Lack of fibrin strands. 3.Attachment to the underlying vessel wall Almost always has a point of attachment. Lacks attachment to the underlying vessel wall. 4.Lines of Zahn May be present Absent 5.Dryness Dry Moist 6.Site of formation In the living circulation Clotting after death and also in extravascular accumulations of blood.
  • 24.
    Difference between fresh& menstrual blood Point Fresh blood Menstrual blood 1. Clot formation Occurs Not occurs 2.Colour Bright red Dark red 3.Odour Salty odour Fishy odour 4.Viscosity Less viscid More viscid 5.Reaction Alkaline Acidic 6.Presence of endometrial and vaginal epithelial cell Absent Present 7.Presence of micro organism Absent (except disease) Lactobacilli, Trichomonas vaginalis, Candida albicans etc are present.
  • 25.
    Difference between male& female blood Traits Male blood Female blood 1. Sex chromatin in leukocytes 44+XY 44+XX 2. Davidson’s body in neutrophil Absent Present in upto 69% neutrophils of females
  • 26.
    Blood group • Redcell membranes have antigens on their external surfaces • These antigens are – unique to the individual – recognized as foreign if transfused into another individual – promote agglutination of red cells if combine with antibody – more than 30 such antigen systems discovered • Presence or absence of these antigens is used to classify blood groups • Major blood groups – ABO & Rh
  • 27.
    Genotype & Phenotype ABOsystem AA.–A AB.– B OO – O AB – AB MN System AM. –M AN.– N MN – MN Rh Factors Rh+ve Rh-ve
  • 28.
    ABO Blood Groups •Most well known & clinically important blood group system. • Discovered by Karl Landsteiner in 1900 • It was the first to be identified and is the most significant for transfusion practice • ABO blood group consist of o two antigens (A & B) on the surface of the RBCs o two antibodies in the plasma (anti-A & anti-B)
  • 29.
    Reciprocal relationship betweenABO antigens and antibodies
  • 30.
    ABO antigens &corresponding antibodies
  • 31.
    Inheritance of ABOBlood Groups • Follows Mendelian principles • Blood group antigens are “codominant”- if the gene is inherited, it will be expressed. • There are three allelic genes -A, B & O • Some aberrant genotypes do occur but they are very rare. • Understanding of basic inheritance important.
  • 32.
    Inheritance of ABOBlood Groups • Two genes inherited, one from each parent. • Individual who is A or B may be homozygous or heterozygous for the antigen. o Heterozygous: AO or BO o Homozygous: AA or BB • Phenotype is the actual expression of the genotype, ie, group A • Genotype are the actual inherited genes which can only be determined by family studies, ie, AO.
  • 33.
    Example of DeterminingGenotype • Mother’s phenotype is group A, genotype AO • Father’s phenotype is group B, genotype BO
  • 34.
  • 35.
    Rh typing • Normaltyping for Rh antigens only includes typing for Rh (D). • The result of this typing determines the Rh status of the cells (Rh - positive or Rh - negative). • Some Rh typing sera is diluted in high protein solutions and may require a negative control. • It is recommended to use two monoclonal anti-D sera from two different manufacturers labeled as D1 and D2, especially to confirm all Rh negatives
  • 36.
  • 37.
    Rh+ve & Rh-veblood type Genotype Blood type (+,-) or (+,+) Rh+ ( - ,-) Rh-
  • 38.
    Importance of bloodgrouping 1.Disputed paternity 2.Disputed maternity 3.Source of blood 4.Stains due to body fluid 5.Identity 6.Cause of death 7.Miscarriage 8.Assist in matching in disaeter.
  • 39.