Forensics Flashcards

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1
Q

What is forensic science?

A

The application of scientific methods and techniques to matter under investigation by court of law. It is used to support legal decision making by providing evidence.

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2
Q

What is Locard’s principle?

A

Every contact leaves a trace

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3
Q

What is meant by physical fit?

A

Comparing two items that were once part of a single item- can be used to prove beyond reasonable doubt the connection between a crime and a suspect. e.g. glass shards that fit together, paint the has scraped off a car at the crime scene

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4
Q

What is trace evidence?

A

Very small amounts of material that provide a link to someone or something e.g. blood, hair, DNA, clothing fibers, paint, soil.

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5
Q

What is the difference between inceptive evidence and reactive evidence?

A

Inceptive evidence is finding evidence that paints a picture of a perpetrator
Reactive evidence is finding evidence that links to a suspect

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6
Q

What factors make trace evidence more valuable?

A

A large amount of material- a lot to analyze, how persistent the material is- how well the material sticks, evidence value- how rare the material is.

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7
Q

How can trace evidence be recovered?

A

Many different techniques such as brushing, taping, shaking, vacuuming, swabbing, pipetting, hand picking and extracting.

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8
Q

How can glass be analyzed?

A

Glass can be analyzed and matched by color and thickness, physical analysis, or chemical analysis using a scanning electron microscope (SEM) or energy dispersive x-ray analysis.

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9
Q

What information can glass craters give about bullets?

A

Glass shards can have the physical fit principle applied. The wider side of the crater is the side the bullet exited, if multiple bullets have pierced glass, the order of impact can be determined by the intersecting cracks.

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10
Q

What are fibres?

A

Any long thin flexible solid object, that is longer than it is wide. Some fibers are more rare than others so have more strength in court.

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11
Q

How can fibers be collected and analyzed?

A

Fibers can be collected through taping, and analyzed by looking under a microscope. Thin layer chromatography can give information on the dyes in fibers. Infrared spectroscopy can be used on artificial fibres.

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12
Q

How is hair analysed?

A

Hair can be identified as human or animal hair, the area of the body where hair came from can be identified, the race of the host can be identified, any artificial altercations such as die can be seen.

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13
Q

How can common bodily fluids like semen and saliva be analysed?

A

Semen can be identified under a microscope, or by looking for acid phosphatase, or by looking for p30 which is in seminal fluid so is useful for sterile individuals. Semen has DNA so can undergo DNA analysis.
Saliva may have traces of DNA from cheek cells, it can be tested for by starch/iodine or salivary amylase.

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14
Q

How can blood be used for analysis?

A

Blood can be classified into animal or human blood, blood group and type, and sex, age and race of the source. Red blood cells and platelets have no DNA but white blood cells do.

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15
Q

How can a crime scene be checked for blood?

A

Through visual analysis, but blood may have been wiped or cleaned. Leachomalachite green or the kastle meyer test can be used to test for blood. LMG is oxidised and becomes green or phenolphthalein is oxidized and becomes pink. Luminol can be used to test for the presence of haemoglobin and can be seen under UV light. Luminol + H2O2 = 3 aminophthalate (produces UV)

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16
Q

How can the pattern of blood be analysed?

A

Blood pattern analysis can give information about the sequence of events of a crime. This can be used to create a timeline and give information about the position of the victim and evidence of struggle. This can be matched against witness statements.

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17
Q

What are the different types of blood pattern?

A

Passive: drops due to gravity, pools. Not related to movement. The shape of the drops is effected by the target surface.
Transfer- wet bloody surface transfers blood to another surface- smear/ wipe. Indicates movement.
Projected- Active blood splatters can come from an arterial gush, or can be cast off stains from a weapon which can tell about the velocity of the impact and the point of convergence.

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18
Q

How is the value of trace evidence determined?

A

How much evidence there is, what the rarity of the evidence is, the combined amount of trace evidence, the presence of alternative innocent sources, how reputable the trace evidence is (how much it links to a single person), how relevant it is to the crime and how well funded the analysis has been.

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19
Q

What is the difference between pharmacodynamics and pharmacokinetics?

A

Pharmacodynamics relates to what a drug does to the body. It is the study of the biochemical, physiologic and molecular effects on the body, involving receptor binding, post receptor effects and chemical interactions.
Pharmacokinetics is what the body does to a drug, it is the movement of the drug through the body and eventually out. The time course of its absorption, distribution, metabolism and elimination.

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20
Q

What is the path of absorption and distribution of alcohol?

A

Alcohol is ingested through the most, goes down the esophagus into the stomach and small intestine where it is absorbed into the circulatory system and distributed amongst the all organs of the body including the brain, kidneys, lungs and liver.

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21
Q

What is alcohol metabolism?

A

The process in which the body breaks down alcohol and eliminates it, most of this is done in the liver.

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22
Q

How quickly is alcohol absorbed?

A

Alcohol is absorbed between 15-45mins after consumption. The absorption rate depends on quantity, concentration, contact time in the GI tract, food and stomach emptying time.

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23
Q

How much alcohol is distributed to each organ?

A

The amount of alcohol distributed to each organ is proportionate to the water content of each organ. The alcohol in the organs reaches equilibrium with the alcohol in the bloodstream.

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24
Q

What effects do blood alcohol levels relate to?

A

Under 50- not obvious
50-100- tipsy, slurred speech, bravado
100-150- abnormal walking pattern, some nausea
150-200- nausea, non co-operative
200-300- probable coma
300-400- coma, impaired respiration
400+ death from respiratory paralysis

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25
Q

How much alcohol is metabolized and what is the rate?

A

90% of alcohol is metabolised, the rest is excreted directly. Blood alcohol level is reduced by around 18mg/hour but can range between 9-27. The variance in rate is due to genetics- it depends on which alcohol dehydrogenase isozyme you have. The rate of metabolism does not change with the addition of reduction of alcohol- zero order kinetics.

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26
Q

What is the pathway of alcohol metabolism?

A

Alcohol is typically broken down into acetaldehyde by alcohol dehydrogenase (rate determining) and then into carbon dioxide and water by aldehyde dehydrogenase. There is two other rare metabolism paths for alcohol: the catalase pathway and the cytochrome p450 pathway. The cytochrome pathway produces free radicals that damage the liver but is typically only used when alcohol dehydrogenase is saturated.

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27
Q

What is legal driving blood alcohol conc in all nations in UK and how is this converted to breath alcohol?

A

50mg in Scotland, 80mg in the rest. Divide by 2300 for breath alcohol. Times by 1.3 for urine alcohol.

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28
Q

What are the accuracies of measurements of alcohol concentration?

A

Blood is the most accurate, it is a measurement of the amount of alcohol effecting the brain. Urine only provides a mean value over the period of excretion. Breath alcohol is in equilibrium with blood, is useful for roadside tests but does not provide evidence.

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29
Q

How can alcohol be analysed

A

By biochemical analysis: ADH requires a co-enzyme (NAD+) to oxidize alcohol. This reduces the co-enzyme (NADH) which can be measured to find BAC by calorimetrically or spectrophotometrically.
Chemical: by electrochemical fuel cell breathalyzers, which are used to make arrests so more accurate tests can be carried out such as infrared optical sensor breathalysers.

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30
Q

How does an electrochemical fuel cell work?

A

Alcohol breath passed through a tank from an anode (-) to a cathode (+). The rate of positive ions, directly related to alcohol concentration, changes depending on increasing concentration. Some ions are captured in the electron rich pads either side, which is dependent on breath alcohol conc, so it can give a reading.

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31
Q

How does an infrared optical sensor work?

A

Infrared waves are passed through a tube. Alcohol breath is blown into the tube and the alcohol blocks some infrared allowing the infrared to be measured at the end of the tube and give a measure of BAC.

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32
Q

What is forensic toxicology?

A

The study of the effects of alcohol, drugs or poisons with application to the law. This is involved in post-mortem toxicology, human performance and drug testing.

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33
Q

What is paracelsus’ third defence?

A

Everything is poison depending on the dose. All substances can harm the body if a large enough dose is taken.

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34
Q

What is a controlled drug?

A

A drug which the manufacture, possession and use of is controlled by the government. Drugs are separated into classes based on their danger to society, the higher the class the more severe the sentence.

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35
Q

What are temporary class drugs?

A

New drugs with 1 year temporary bans put on them to allow the government to assess the danger of the drug and classify it. These new drugs often have similar chemical structures to others and provide legal highs.

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36
Q

What are the different types of drugs?

A

Stimulants: drugs that stimulate brain activity in the prefrontal cortex e.g. cocaine, amphetamines
Depressants: drugs which inhibit brain activity e.g. alcohol, heroin
Hallucinogens: drugs which induce alterations in perception and mood e.g. LCD, mushrooms, cannabis, MDMA

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37
Q

How can drugs be analysed and what information can this tell you?

A

Drugs can be analysed through presumptive tests such as dipstick urine tests, or accurately through chromatography to identify drugs through their weight and charge. Mass spectrometry, immunoassays or spectroscopy can also be used. This can tell you what drugs are present in a sample, and can produce unique chemical signatures that link them back to gangs.

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38
Q

How can gas chromatography be used to analyse a drug?

A

Gas chromatography separates the individual components of a drug based on weight and charge and shines infrared light through this to produce a graph of peaks. These peaks are different depending on the weight and polarity giving each drug a unique signature. This can also identify contaminants.

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39
Q

Why is hair analysis often used in workplace drug testing?

A

Hair traps drugs in the base of the cells- melanin and stays present in the hair as it grows. This hair can then be heated and traces of drugs such as cocaine and heroin can be found. Urine and saliva testing only gives a recent profile.

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40
Q

What is pharmacogenetics?

A

The study of genetic influence on the ADME process.

41
Q

What does the concentration dose curve measure and what does this show?

A

Measures the percentage response from different doses of a drug. This can show the
LD50- Lethal dose for half the population (50%).

42
Q

What can affect the toxicity of a drug?

A

Sensitization: the second exposure to a drug will have a enhanced immune response.
Tolerance- when repeatedly exposed, develop reduced reaction
Accumulation- the rate at which the drug is removed
Bioavailability: how much of the dose is absorbed and the rate at which the dose is absorbed,

43
Q

How can blood be used in forensic analysis?

A

Blood can be grouped depending on the type of antibodies, antigens and proteins present. There is no DNA in red blood cells. This can be used to quickly eliminate suspects based on blood type.

44
Q

What are the different types of blood ABO groups?

A

Blood type A: red cells have A antigens and serum has anti-b antibodies
Blood type B: red cells have B antigens and serum has anti-a antibodies
Blood type AB: red cells have A and B antigens and antibodies against neither
Blood type O: red cells have no antibodies and antigens against both A and B.
O is a universal doner and AB is a universal acceptor.
Rhesus is a protein which gives positive and negative groupings. Other immunological markers include: Duffy, Km, Kell, MNS. PGM is another immunological marker found in semen.

45
Q

What are secretors?

A

Secrete antigens into other bodily fluids which can be used to identify blood type. 75-85% of the population

46
Q

What is the history of DNA sampling?

A

Discovered by (sir) alex jeffreys by chance. It was first used to convict colin pitchfork by linking crimes to one another.

47
Q

What can DNA profile be used for?

A

To link crimes to one another, and to link suspects to samples found at the murder scene.

48
Q

What are examples of good sources of DNA?

A

White blood cells, hair roots, vaginal fluid, sperm.

49
Q

What are examples of bad sources of DNA?

A

Urine, hair shaft, faeces and skin cells. Skin cells often have environmental damage and skin cells that shed are dead.

50
Q

What are DNA profiling markers used on autosome?

A

STRs: Short tandem repeats- repeated DNA sequences with large variation across the population. Have very high discrimination power but are not useful on very degraded DNA.
SNPs: Single nucleotide polymorphisms- do not have high discrimination power and are not useful with DNA mixtures but are available on very degraded DNA.

51
Q

What DNA markers can be used on the Y-chromosome?

A

STRs: useful where there is a mixture of male and female DNA. Used to identify the male in the mixture, the discrimination power is lower than autosomal due to less STR regions and direct heritability down patriline.

52
Q

What DNA markers can be used on mitochondrial DNA?

A

SNPs (in a control region): High copy number of mitochondrial DNA so there is good survival of DNA, but low discrimination power as there is not much difference across the population and direct heritability down matriline.

53
Q

What is the issue with twins and DNA profiling?

A

Identical twins share 100% of their DNA so it is difficult to differentiate between them. This allows one to blame the other such as in the Rosslyn chapel case.
Methylation profile can be used to tell the difference between twins, as this varies according to environmental factors.

54
Q

How can STRs be analysed?

A

Restriction fragment length polymorphism analysis: Large amounts of DNA required and undegraded material. DNA is cut at certain points depending on short tandem repeats, so resultant strands will be different lengths. Can then be measured using gel electrophoresis.
Polymerase Chain Reaction: less DNA required, can be partially degraded.

55
Q

How can changes arise in short tandem repeats?

A

Slippage of DNA polymerase results and subsequent misalignment of DNA polymerase results in addition or subtraction of nucleotide sequence repeats.

56
Q

What is mini-sequencing used to analyse and how does it work?

A

Sequences a particular region to check for one base or another at that locus. Allows SNPs to be identified.

57
Q

What is the primary use of mitochondrial DNA?

A

A mitochondria only has 37 genes on the molecule. It is typically useful for identifying individuals that belong to the same family and linking bodies together. It can also be used to track maternal relation.

58
Q

What is the amelogenin locus?

A

This is an important locus for identifying males and females in a sample. This locus is used to form enamel, and has a six base pair deletion on the X chromosome not present on the Y. This can tell how many males and females are in the sample by the size of peaks of the X and Y chromosomes.

59
Q

What are the applications of DNA profiling?

A

Familial searching, solving cold cases, linking/identifying families, wildlife crime.

60
Q

How much DNA is needed for DNA databases around the world?

A

USA combined DNA index system (CoDIS): 20 Loci (used to be 13)
National DNA Database (NDNAD) (UK): DNA-17 in England, 21 STR loci and two Y markers in Scotland. Used to be 11 (1 Y).

61
Q

How much of the population are in the DNA database?

A

UK-8%
USA-6%

62
Q

What is the probability of having unique DNA on the CoDIS database?

A

1 in ten trillion, unless you have a twin. The world only has a population of 7.5 billion.

63
Q

Can DNA evidence be used in court?

A

No DNA evidence cannot be used solely for evidence as there are many sources of error:
-Degraded DNA
-Human Error: with lab equipment
-Technical Failure: with lab equipment
-Contamination: public spaces have al lot of DNA
-PCR slippage: big issue if it happens early in the process cause the repeat number does not match the sample DNA.

64
Q

What is low copy number analysis?

A

LCN analysis takes DNA from a much smaller sample and copies 10 informative sites (STR). This has the same discrimination power as routine DNA profiling but takes longer to process and may only build a partial profile

65
Q

What is a partial profile?

A

A partial profile is an incomplete DNA profile, it has missing alleles/ STR loci. This may get multiple matches but can usually be narrowed down by police intelligence and familial searching.

66
Q

What is familial searching?

A

When the DNA doesn’t match any profile on the data base, similar profiles can be looked for in order to try find close relatives of the perpetrator. This can be paired with ethnic and gender markers to increase search accuracy.

67
Q

How was familial searching used in the M3 murder?

A

Bricks thrown onto traffic off a footbridge above the M3 when Renault Clio was being stolen. DNA from the brick and the Clio was used to build a DNA profile. It was narrowed down to a white male under 35. 16-20 matches showed up after familial searching- led to craig Harman.

68
Q

How have cold cases been solved using DNA analysis?

A

Advances in DNA technology and development of DNA boost (computer based analysis system to interpret DNA mixtures) have allowed cold cases to be revisited.

69
Q

When was familial searching first used on the NDNAD?

A

Operation magnum: Familial searching was used to link 3 murders together- 2 murders linked to another and led to exhumation of body of joseph kappen through familial searching.

70
Q

How was familial searching used to identify the shoe rapist?

A

DNA was taken from a sister who had a sample taken when drink driving, linking to conviction and confession of James Lloyd.

71
Q

How was mitochondrial DNA used to dispute claims in the Romanovs?

A

DNA was taken from the mass grave of the Romanovs and mtDNA was compared with living relatives. Unbroken female lineage and the Tsars brothers DNA. Woman who claimed to be missing child didnt match the DNA.

72
Q

How can DNA be used for identification?

A

In natural disasters, there are a lot of bodies which need to be identified. Profiles from blood and bone in these samples can be compared with living relatives to confirm bodies. Difficult when whole family have been killed.

73
Q

What did the world trade centre lead to in DNA profiling?

A

New DNA extraction methods from bone, new molecular techniques to extract DNA exposed to high heat.

74
Q

What other applications does DNA profiling have?

A

DNA profiling can be used to study genetic diseases. This can be done by comparing genes from healthy to diseased individuals. This differs from forensic profiling as these dont look at whole genes, just STRs in regions which dont encode genes.

75
Q

How can DNA profiling be used in relation to wildlife and animal crime?

A

DNA profiling can be used to see where wildlife has come from e.g. ivory tusks or wet markets.
Pets can link owners to a crime, if pet material e.g. hair found on the crime scene. Profiling can also be used to prove a pet was involved in a crime, like a dog bite.
This technique can also identify the origin of meat e.g. horse meat scandal.
These techniques are quite expensive and are typically only used where conviction would hang on the evidence.

76
Q

What are some of the ethical issues surrounding DNA profiling?

A

Although everybody being profiled would make many more crimes solvable, this could leave to unfair convictions due to the sources of error in DNA profiling. Also seen as an invasion of privacy, as it is putting alot of trust in the government.

77
Q

What is forensic entomology?

A

The study of insects (and their larvae), and arthropods to aid forensic investigations. This is primarily used in unnatural death investigations, but can be used to detect drugs and poisons, determine the location of an incident and find the presence and time of infliction of wounds.

78
Q

What are the three areas of application of forensic entomology?

A

Insects that inhabit human remains, insects that damage structures and infestation of foods.

79
Q

What is the post mortem interval?

A

The interval between time of death and post mortem exam- how long before discovery was a body dead.

80
Q

How can insects be used to work out the PMI?

A

Insects can be studied to work out how long they have colonized a body for, which can then be used to work out the post mortem interval.

81
Q

How can insects be used as evidence?

A

Insects arrive in a very consistent set pattern in order to colonize a body, known as the season of death. The insects present and their stage of life can indicate PMI.
If there has been a change in location since death, the insects on the body can reflect that- insects should match the environment.
The insects can give information about the circumstances surrounding the death, such as if the body was buried, or in contact with water, or if drugs were involved (toxicology).

82
Q

What is metaphorphosis?

A

How an insect develops from an immature form to an adult through different distinct phases. This allows us to tell the age of the insects. Development time can vary depending on temperature.

83
Q

What is succession in relation to insects and forensics?

A

Succession is the set pattern that insects arrive at a body. This is consistent so allows age of the body to be estimated.

84
Q

Why are insects so successful?

A

Insects go through metamorphosis and different stages eat different foods- lowers competition.
Insects have different feeding patterns across species so do not compete with each other and have adapted physiological and biomechanical methods for this.
Insects have a very small size, an exoskeleton that creates a protective barrier (chitin), and wings which allow for quick movement.
Insects have very quick lifecycles allowing for fast evolution.

85
Q

How can insects be collected?

A

A net to catch flying insects, a collecting pot to store and label insects and a specimen jar for insects/larvae.

86
Q

What is the lifecycle of a blow fly?

A

Adult blowflies arrive at the body within minutes and lay eggs in wounds- 300 eggs.
Eggs hatch into 1st star larvae within 24 hours.
They feed and moult to second instar larvae and then third stage maggots.
They then moult to prepupae larvae and move away from the body,
They finally moult to pupae and then into an adult.
5 stages in metamorphosis before adult.

87
Q

How can micro-organisms be used in forensic science?

A

Humans host many microbes. Bacteria are important to the decay process, which is effected by environmental factors. Dry/frozen environments slow down decomposition, Warm and moist environments speed up decomposition. Ongoing research into the possibility of using microbes to determine PMI.
Microbes can be used as identification tools however, can tell about the nature of a death.
Microbes such as soil microbes, saliva microbes, infective microbes and food poisoning are relevant to forensic science.

88
Q

Why is PMI important?

A

It creates a timeline for police to support or refute witness statements.

89
Q

What can be used to calculate PMI?

A

Physical evidence: post-mortem changes, presence of insects
Environmental evidence: indoor, outdoor, buried, submerged
Historical evidence: victims daily habits. relationships
Additional evidence- stopped watch, phone record.

90
Q

What is algor mortis?

A

Algor mortis is the first stage of decomposition. It is the cooling of the body temperature. 98.6 degrees Fahrenheit is standard body temperature. Internal temperature and average cooling rate can be used to calculate PMI.
Hours since death = (98.6 - int temp)/1.5

91
Q

What may affect the cooling of the body (algor mortis)?

A

Body size, body fat percentage, body position, external environment, clothing, body dismemberment.

92
Q

What is rigor mortis?

A

Stiffening of the muscles after death of an individual. Due to reduction in available ATP for muscles. This effects the smaller muscles first, then the larger muscles. The first signs can be seen within 3-6 hours and it will be completely disappeared by 24-36 hours. Max rigor is seen between 6-12 hours. This is affected by temp, muscle mas and if there was physical activity before death.

93
Q

What is livor mortis (hypostasis)?

A

This is settling of the blood due to gravity. The blood stops being pumped and will pool in areas of the body. Pale areas are areas which have had pressure on them. This is not useful in calculating PMI but can give an idea of body positioning, and if the body has been moved.

94
Q

What are the stages of post mortem decomposition?

A
  1. Fresh- body begins to cool- mortis stages
  2. Bloat- discoloration of skin, body swells from gas accumulation, soft tissues begin to decay.
  3. Active decay/ putrefaction- tissues begin to liquify, skin begins to blacken, body deflates (purge)
  4. Advanced decay- Progressive loss of soft tissue, decay by invertebrates and microbes begins to slow as body dries out
  5. Dry remans- skin and soft tissue lost, decay proceeds more slowly.
95
Q

What are the visible features of decomposition leading to bloat and purge?

A

First a greenish discoloration is seen in the lower right quadrant and then through the body, due to breakdown of haemoglobin by intestinal bacteria.
Skin slippage and blistering is then observed as the epidermis separates from the dermis.
The skin begins to marble as bacteria from the abdomen spread via blood vessels, resulting in dark purple/green veins.
The body then begins to bloat as gases build up as a by-product of decomposition.
Purge then occurs where tissues begin to liquify and gases escape resulting in the body deflating.

96
Q

What are the two modifications of the decomposition process?

A

Mummification: Happens in very dry environments (hot or cold), where the kin dries out and gives a leathery appearance.
Adipocere: Happens in damp environments where water replaces body fat giving the body a waxy appearance. This tends to occur in bodies submerged in water.
These processes partially preserve the bodies and features.

97
Q

What is the total body score?

A

Decomposition is a very sequential process. A visual analysis of the body can be applied to the total body scoring system to calculate PMI. This rates the head, trunk and limbs of the body depending on their stage of decay. TBS adds theses scores together and with temperature can be used to calculate PMI.

98
Q

How can PMI be calculated using total body score?

A

Temperature accounts for 80% of the variation in decomposition. This can be measured using accumulative degree days- the total temperature a body has been exposed to. Using the equation-
ADD = 10^ TBSTBS0.002+1.81 (+-388.16).
The ADD can be matched to the degrees per day to work out the time of death.