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Forensic Entomology

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Title: Forensic Entomology


1
Forensic Entomology
  • Maggots and Time of Death Estimation

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Entomology is the Study of Insects Images from
www.afpmb.org/military_entomology/usarmyento/files
/ArmyEntomology.ppt
4
Insect Biology
  • Insects are the most diverse and abundant forms
    of life on earth.
  • There are over a million described species- more
    than 2/3 of all known organisms
  • There is more total biomass of insects than of
    humans. of humans.
  • Insects undergo either incomplete or complete
    metamorphosis (Egg to larva to pupa to insect)
  • Larva have a soft tubular body and look like
    worms. Fly species larvae are maggots

5
What is Forensic Entomology?
  • Forensic Entomology is the use of the insects and
    other arthropods that feed on decaying remains to
    aid legal investigations. 
  • Medicolegal (criminal)
  • Urban (criminal and civil)
  • legal proceedings involving insects and related
    animals that affect manmade structures and other
    aspects of the human environment
  • Stored product pests (civil) 

6
Medicolegal Forensic Entomology
  • Often focuses on violent crimes
  • Determination of the time (postmortem interval or
    PMI) or site of human death based on
    identification of arthropods collected from or
    near corpses.
  • Cases involving possible sudden death
  • Traffic accidents with no immediately obvious
    cause
  • Possible criminal misuse of insects

7
Postmortem interval (PMI)
  • Forensic Entomology is used to determine time
    since death (the time between death and corpse
    discovery)
  • This is called postmortem interval or PMI).
  • Other uses include
  • movement of the corpse
  • manner and cause of death
  • association of suspects with the death scene
  • detection of toxins, drugs, or even the DNA of
    the victim through analysis of insect larvae.

8
Forensic Entomology is Applied Biology
  • If it werent for decomposition of all living
    things, our world would fill up with dead bodies.
  • When an animal dies, female insects will be
    attracted to the body. They enter exposed
    orifices or wounds and lay eggs or larvae.
  • A forensic entomologist
  • identifies the immature insects
  • determines the size and development of the
    insects
  • calculates the growth of the insects and passage
    through stages of the life cycle in laboratory
  • compares the growth against weather conditions to
    estimate time of oviposition

9
Succession of Insects on the Corpse
  • Estimates of postmortem intervals based on
    insects present on the remains are based on
  • The time required for a given species to reach a
    particular stage of development.
  • Comparisons of all insect species present on the
    remains at the time of examination.
  • Ecological succession occurs as an unexploited
    habitat (like a corpse) is invaded by a series of
    different organisms.
  • The first invasion is by insect species which
    will alter the habitat in some form by their
    activities. These changes make the habitat
    attractive to a second wave of organisms which,
    in turn, alter the habitat for use by yet another
    organisms.

10
Ecology of Decomposition
  • Necrophages - the first species feeding on corpse
    tissue. Includes rue flies (Diptera) and beetles
    (Coleoptera).
  • Omnivores - species such as ants, wasps, and some
    beetles that feed on both the corpse and
    associated maggots. Large populations of
    ominvores may slow the rate of corpses
    decomposition by reducing populations of
    necrophagous species.
  • Parasites and Predators - beetles, true flies and
    wasps that parasitize immature flies.
  • Incidentals pill bugs, spiders, mites,
    centipedes that use the corpse as an extension of
    their normal habitat

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Image http//www.nlm.nih.gov/visibleproofs
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Decay Rates Are Variable
  • Studies of decay rates of 150 human corpses at in
    the Anthropological Facility in Tennessee (The
    Body Farm)
  • Most important environment factors in corpse
    decay
  • Temperature
  • Access by insects
  • Depth of burial
  • Other Factors
  • Chemical-- embalming agent, insecticides, lime,
    etc.
  • Animals disrupting the corpse

13
Time of Death can be broadly estimated up to
about 36 hours
Temperature Stiffness Time of death
Warm Not stiff Dead less

than three hours
Warm Stiff Dead between 3

to 8 hours
Cold Stiff Dead between 8

to 36 hours
Cold Not stiff Dead in more

than 36 hours
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  • Temperature Stiffness Time of Death

16
Differentiate between PMI and Time of Death
  • These may not always equate.
  • Post mortem interval is restricted to the time
    that the corpse or body has been exposed to an
    environment which would allow insect activity to
    begin.
  • Closed windows
  • Body in box or bag
  • Cold temperatures
  • Deeper burial

17
Insect species arrive at a corpse in waves like
clockwork
  • Calculate the heat/thermal energy (accumulated
    degree hour) required for each stage of the Green
    Bottle Flys life cycle.
  • Possibly the greatest potential source of error
    in using arthropod successional patterns lies in
    the collection of speciments.
  • Must only be done correctly to accurately sample
    the insects.

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Image http//www.nlm.nih.gov/visibleproofs
19
Calculating PMI from Accumulated Degree Hours
(ADH)
20
Calculating ADH from Climate Data
21
Using the Data
  • 3928 ADH in these three days (95214881488).
  • How many ADH of 70º are there in these 3 days?
  • 3928/7056.11 hours
  • 72 hours at 70º would have the insects passing to
    the 3rd instar. But 72 hours at colder
    temperatures and insects will only be at 2nd
    instar stage.

22
Five Stages of Decomposition Fueled by Insect
Activity.
  • Fresh
  • Bloat
  • Decay
  • Post-decay
  • Dry (skeletal)

23
Fresh
  • Begins at death
  • Flies begin to arrive
  • Temperature falls to that of the ambient
    temperature.
  • Autolysis, the degradation of complex protein
    and carbohydrate molecules, occurs.

24
Bloat
  • Swells due to gases produced by bacteria
  • Temperature rise of the corpse
  • Flies still present

25
Decay
  • Gases subside, decomposition fluids seep from
    body.
  • Bacteria and maggots break through the skin.
  • Large maggot masses and extreme amounts of fluid.
  • Unpleasant odor
  • Larvae beginning to pupate.
  • Corpse reduced to about 20 of its original mass.

26
Post-Decay
  • Carcass reduced to hair, skin, and bones.
  • Fly population reduced and replaced by other
    arthropods.
  • Hide beetles are dominant in dry environments.
  • Mite and predatory beetle populations increase.

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Dry (Skeletal)
  • Does not always occur especially if corpse is in
    a wet region. Maggots will stay longer and hide
    beetles will not appear.
  • In wet environments the hide beetles are replaced
    with nabid and reduviid insects.
  • The corpse is reduced to at least ten percent of
    the original mass.
  • In the last stage (Skeletal Stage), only bone and
    hair remain.

28
Methods
  • This project took place at the Huntington
    landfill beginning on September 5, 2003.
  • Two different areas were chosen to deposit two
    pigs.
  • Pig 1 was laid in a sunlit area.
  • Pig 2 was laid in a shaded woodland area about
    100 feet away at an elevation of approximately 20
    feet.

29
Methods
  • Both pigs were placed in cages constructed of
    wood and one inch chicken wire that were staked
    to the ground to protect from predatory animals.
  • Prior to starting the project, great care was
    taken to prevent insect activity from taking
    place. After they died, the pigs were
    individually tied in two black garbage bags,
    placed in feed sacks, and secured.

30
Methods
  • The pigs were kept at -80C in the laboratory.
  • They were placed in plastic bins in order to thaw
    for 48 hours prior to placement at the landfill.
  • Closed environment was maintained until they were
    deposited at the site.

31
Methods
  • Pigs with a genetic line of a minimum of fifty
    percent Yorkshire.
  • They were 8-10 weeks old and weighed
    approximately 40-50 pounds.
  • Both died on July 11, 2003 approximately 12 hours
    apart. One died a natural death and the other
    was culled from the litter.
  • Both of the carcasses were in very similar
    condition there were no breaks, tears or cuts in
    the skin.

32
Methods
  • Daily observations were made at both sites
    throughout the day at 7am, 1pm, 7pm, and 1am.
  • Air, ground, and maggot mass temperatures were
    taken at each visit and observations were
    recorded.
  • At 7am and 7pm they also collected maggot samples
    for analysis and photographed the scene.
  • Observations were noted and samples taken for a
    period of nine days.

33
Methods
  • Using insect tweezers, the investigators
    collected a number of maggots and dropped the
    samples immediately into boiling water, to kill
    the bacteria in the maggots and also to
    straighten their bodies for easier analysis.
  • The maggot samples were taken from different
    areas of the body in which there were large
    numbers present.

34
Methods
  • The maggots were then placed into a labeled jar
    and preserved with 70 EtOH.
  • They also collected interesting arthropods for
    analysis.
  • All of the samples were labeled and stored for
    later analysis in the laboratory.

35
Phormia regina
Spiracles are incomplete Third-instar larvae
36
Phaenicia species
Spiracles are complete Third-instar larvae
37
Results Fresh Stage
  • Flies began to arrive within minutes of pig
    placement however, laying of eggs was delayed
    12-18 hours.
  • There was already some green discoloration on Pig
    2 at the beginning of the fresh stage, possibly
    due to the fact that it was dead about 8 hrs
    before Pig 1.
  • 72 hrs later, the first signs of bloating
    occurred, ending the Fresh Stage.

38
Results Bloat stage
  • At about 72 hours, noticeable bloating began to
    occur in Pig 1.
  • However, Pig 2 did not show visible signs of
    bloating until about 92 hours.
  • The gap between the two pigs might have been even
    greater if they had both died at exactly the same
    time.

39
Results Decay Stage
  • Decay stage started around 102 hours.
  • At this point, the maggots had broken the skin
    and the pigs had begun to deflate.
  • Decompositional fluids began to seep from the
    carcass.
  • There was a green froth around the pig and also a
    dark fluid ring around the body of Pig 1.
  • Maggot activity increased tremendously, and
    maggot mass temperature reached its high during
    this stage.

40
Results Post-decay Stage
  • When the experiment was terminated due to the
    fact that maggot activity had ceased, the pigs
    had reached the Post-Decay Stage.
  • They were mostly skin, bones, and hair, but there
    was some tissue remaining.

41
Temperature is a Factor Pig 1
  • The graph shows an elevation for maggot mass
    temperatures over ambient
  • The fluctuation in ambient temperature induced
    elevated maggot activity which is consistent with
    other similar experiments.

Sunlit Pig
42
Temperature is a Factor Pig 2
  • The ambient temperature for Pig 2 was more
    constant because it was in a shaded area.
  • The temperatures for Pig 1 fluctuated more than
    those of Pig 2.

Shaded Pig
43
Phormia Average Maggot Length vs. Time
  • Shows a gradual increase then decrease for the
    Phormia regina
  • The maggots feed and grow to a certain point when
    they begin to leave the carcass to find a safe
    place to pupate.

44
Phaenicia Average Maggot Length vs. Time
  • Two peaks for the Phaenicia
  • Infers two generations for Pig 1.

45
Two Different Maggot Generations
  • These are distinguishable by the length and
    obvious size difference.
  • This is why we believe there are two peaks in our
    graph data for the Sunlit Pig.
  • The photograph was taken at a time consistent
    with the influx at 132 hours.

46
Discussion
  • Two different species of maggots were collected
    over the nine day period.
  • These two species were analyzed at their third
    instar stages they were able to determine the
    difference by comparing their spiracles.
  • The third instar was the only stage that they
    analyzed species determination was more evident
    at this stage of development.
  • They also reared a sample of maggots from each
    pig for later species analysis.

47
Accumulated Degree Hours
  • ADH may be calculated using temperature and
    hours.
  • This works because there is direct correlation
    between temperature and maggot development.
  • These calculations were somewhat approximate but
    relatively accurate.

48
ADH and Pig Results
  • ADH for Pig 1 was calculated as 4885.2 after nine
    days.
  • ADH for Pig 2 was calculated as 4488.6 after nine
    days.
  • These can be used to determine PMI for carcasses
    found in this area in similar conditions.

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