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DR SARAH FIELDHOUSE PH.D. Fingerprint sampling devices; Methods for controlling fingerprint deposition

DR SARAH FIELDHOUSE PH.D. Fingerprint sampling devices; Methods for controlling fingerprint deposition

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Page 1: DR SARAH FIELDHOUSE PH.D. Fingerprint sampling devices; Methods for controlling fingerprint deposition

D R S A R A H F I E L D H O U S E P H . D .Fingerprint sampling devices; Methods for controlling fingerprint deposition

Page 2: DR SARAH FIELDHOUSE PH.D. Fingerprint sampling devices; Methods for controlling fingerprint deposition

Friction ridge skin

identification

Advancement of AFIS

Latent mark detection

Latent mark longevity

Latent mark composition

Latent mark development/

recovery techniques

‘fingerprint’ research

Fingerprint research

There are no universally

accepted protocols for carrying out ‘fingerprint’

research.

They all require ‘fingerprints’

Page 3: DR SARAH FIELDHOUSE PH.D. Fingerprint sampling devices; Methods for controlling fingerprint deposition

asking participants to apply ‘moderate pressure’ [1]

asking participants to carry out specific tasks [2]

use of a top pan balance to apply a specified mass, which is then converted to force [4, 5]

use of a fingerprint sampler to control deposition [6]

Examples of existing strategies to control fingermark deposition

researcher assisted deposition [3]

Page 4: DR SARAH FIELDHOUSE PH.D. Fingerprint sampling devices; Methods for controlling fingerprint deposition

1. Variations in force application

2. Variations in contact time between the ridges and the substrate

3. Variations in contact area of friction ridge to surface contact

Variations in fingermark deposition

4 inked fingerprints deposited by the same finger

Page 5: DR SARAH FIELDHOUSE PH.D. Fingerprint sampling devices; Methods for controlling fingerprint deposition

145mm

Deposition force management springs

110mmFinger resistor bar

Deposition platform

Adjustable finger clamp

Finger Rest

The fingerprint sampler

The fingerprint sampler allows consistent and reproducible fingermark deposition,

controlling physical factors associated with deposition [6].

Page 6: DR SARAH FIELDHOUSE PH.D. Fingerprint sampling devices; Methods for controlling fingerprint deposition

• Consistency in surface area• Contact time controlled• No distortion associated with mark deposition, e.g. force• Improved ‘quality’ of marks compared to marks deposited without it’s use [6]

1 2 3 4 5

6 7 8 9 10

Fingermarks deposited using the fingerprint sampler

Page 7: DR SARAH FIELDHOUSE PH.D. Fingerprint sampling devices; Methods for controlling fingerprint deposition

There were two aims to this research project;

1. To develop a fingerprint sampler to facilitate fingermark deposition at different force quantities.

2. To study the effects of different force applications during latent fingermark deposition on the appearance of the resultant marks.

Page 8: DR SARAH FIELDHOUSE PH.D. Fingerprint sampling devices; Methods for controlling fingerprint deposition

Adjustable base

Finger rest

290mm

190mm

Fingerprint deposition platform

Force scale

Direction of movement

Fingerprint sampler 2

Multiple force capability

Page 9: DR SARAH FIELDHOUSE PH.D. Fingerprint sampling devices; Methods for controlling fingerprint deposition

Fingerprint sampler 2

Spring

Fingerprint deposition platform

Finger rest

110mm

Page 10: DR SARAH FIELDHOUSE PH.D. Fingerprint sampling devices; Methods for controlling fingerprint deposition

Hooke’s law of elasticity

0

0.5

1

1.5

2

2.5

f(x) = 0.387492659077273 x + 0.019999740151347R² = 0.999999999845224

Force (N)

Sp

rin

g d

efle

ctio

n (

cm)

Spring calibration

Page 11: DR SARAH FIELDHOUSE PH.D. Fingerprint sampling devices; Methods for controlling fingerprint deposition

Methodology

1. Latent and inked fingermarks were deposited from the same finger at approximate force quantities of 1N-10N at 1N increments onto glass surfaces and photocopier paper.

For latent fingermarks participants were asked to refrain from washing their hands for 1 hour prior to deposition. The fingers were ‘loaded’ against an equivalent area of friction skin, i.e. a finger.

2. The latent fingermarks were then examined using Scanning Electron Microscopy.

3. The latent fingermarks were then developed using CNA fuming

4. Surface plot analysis commenced using a fingerprint digitiser (DCS121)

5. The inked fingerprints were examined for differences in surface area at different forces and consistency between marks at equivalent forces.

Page 12: DR SARAH FIELDHOUSE PH.D. Fingerprint sampling devices; Methods for controlling fingerprint deposition

Results - Scanning Electron Microscopy

1N 5N 10N

Page 13: DR SARAH FIELDHOUSE PH.D. Fingerprint sampling devices; Methods for controlling fingerprint deposition

Results - Surface plot analysis

1N

3N

2N

4N

Page 14: DR SARAH FIELDHOUSE PH.D. Fingerprint sampling devices; Methods for controlling fingerprint deposition

5N 6N

7N 8N

Page 15: DR SARAH FIELDHOUSE PH.D. Fingerprint sampling devices; Methods for controlling fingerprint deposition

9N

10N1N 5N

10N

Page 16: DR SARAH FIELDHOUSE PH.D. Fingerprint sampling devices; Methods for controlling fingerprint deposition

Results - Differences in surface area

12.0

13.0

14.0

15.0

16.0

17.0

18.0

19.0

20.0

21.0

22.0

23.0

24.0

1 2 3 4 5 6 7 8 9 10

Len

gth

(mm

)

Force (N)

Fingerprint length

participant 1 participant 2 participant 3 participant 4 participant 5

Standard Error of the Mean = 0.5mm

Statistically significant differences were found to exist (N15, F72.485, p 0.00). Effect size large (0.838).Bonferroni post hoc tests suggest that these exist between the earlier force increments only. (p≤0.05).

Page 17: DR SARAH FIELDHOUSE PH.D. Fingerprint sampling devices; Methods for controlling fingerprint deposition

Results - Differences in surface area

5.06.07.08.09.0

10.011.012.013.014.015.016.017.0

1 2 3 4 5 6 7 8 9 10

Len

gth

(mm

)

Force (N)

Fingerprint width

participant 1 participant 2 participant 3 participant 4 participant 5

Standard Error of the Mean = 0.5mm

Statistically significant differences were found to exist (N15, F99.622, p 0.00). Effect size large (0.877). Bonferroni post hoc tests suggest that these exist between the earlier force increments only. (p≤0.05).

Page 18: DR SARAH FIELDHOUSE PH.D. Fingerprint sampling devices; Methods for controlling fingerprint deposition

Conclusions

As the force applied to the finger increases;

• the quantity of friction ridge residue transferred to the resultant mark appears to increase, as does ridge depth.

• how the latent mark develops and how a mark is assessed.

• the surface area of the resultant mark increases (to a maximum point), especially important with marks deposited under less force.

Differences in the quantity of force applied by friction ridge skin to a surface during mark deposition will affect the appearance of the resultant marks.

This may affect;

important for fingermark comparisons, e.g. how they change over time

• the consistency of samples in research projects

Page 19: DR SARAH FIELDHOUSE PH.D. Fingerprint sampling devices; Methods for controlling fingerprint deposition

Implications for fingerprint research

As part of a scientific approach to research it is important to recognise and control variables where possible.

Fingerprint samplers represent a simple means of controlling physical variables associated with fingermark deposition.

This approach might help to improve efficiency in the research approach.

Fingerprint samplers can be useful teaching aids.

Page 20: DR SARAH FIELDHOUSE PH.D. Fingerprint sampling devices; Methods for controlling fingerprint deposition

Further information

Dr Sarah Fieldhouse (Staffordshire University), email: [email protected] telephone: 01782 295795

Philip Morton (SciChem), email: [email protected] telephone: 07522 428611

Thank you for listening, any questions?

Page 21: DR SARAH FIELDHOUSE PH.D. Fingerprint sampling devices; Methods for controlling fingerprint deposition

References

[1] Bohanan, A. M. (1998). Latent’s from Pre-pubescent Children Versus Latent’s from Adults. Journal of Forensic Identification. 48(5) p570-573.[2] Given, B. W. (1976). Latent Fingerprints on Cartridges and Expended Cartridge Cases. Journal of Forensic Sciences. 21(3) p587-594.[3] Croxton, R. Baron, M. Butler, D., Kent, T., Sears, V. (2010). Variation in amino acid and lipid composition of latent fingerprints. Forensic Science International. 199(1-3 p93-102.[4] Fieldhouse SJ. (2009) Consistency and reproducibility in the deposition and evaluation of latent fingermarks, contributing to an investigation into the effectiveness of a portable cyanoacrylate fuming system and aluminium powder for latent fingermark development (A thesis submitted in partial fulfilment of the requirement of Staffordshire University for the degree of Doctor of Philosophy). Stoke on Trent: Staffordshire University.[5] Jasuja, P., Toofany, M. A., Singh, G., Sodhi, G. S. (2009). Dynamics of latent fingerprints: The effect of physical factors on quality of ninhydrin developed prints – A preliminary study. Science and Justice. 49(8).[6] Fieldhouse, S., 2011. Consistency and reproducibility in fingermark deposition. Forensic Science International. 207(1-3) p96-100.