Advances in Fingerprint Technology.pdf

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116. Kobus, H.J., Pigou, P.E., Della, E.W., Taylor, B., and Davies, P.J., Fingerprint research in South Australia, in Proc. Int. Symp. on Fingerprint Detection and Identification, Ne’urim, Israel, Almog, J. and Springer, E., Eds., Hemed Press, 1995, 227. 117. Della, E.W., Janowski, W.K., Pigou, P.E., and Taylor, B.M., Synthesis of fingerprint reagents: aromatic nucleophilic substitution as a route to 5-substituted ninhydrins, Synthesis, 12, 2119, 1999. 118. Almog, J., Hirshfeld, A., Frank, A., Sterling, J., and Leonov, D., Aminoninhydrins: fingerprint reagents with direct fluorogenic activity — preliminary studies, J. Forensic Sci., 36, 104, 1991. 119. Almog, J., unpublished results (see Ref. 111). 120. Hark, R.R., Hauze, D.B., Petrovskaia, O., Joullié, M.M., Jaouhari, R., and McKomiskey, P., Novel approaches toward ninhydrin analogs, Tetrahedron Lett., 35, 7719, 1994. 121. Hark, R.R., Hauze, D.B., Petrovskaia, O., and Joullié, M.M., Chemical detection of fingerprints — synthesis of arylated ninhydrin analogs, in Proc. Int. Symp. on Fingerprint Detection and Identification, Ne’urim, Israel, Almog, J. and Springer, E., Eds., Hemed Press, 1995, 129. 122. Hark, R.R., Synthesis of Ninhydrin Analogs, Ph.D thesis (M.M. Joullié, supervisor), University of Pennsylvania, Philadelphia, 1996. 123. Hauze, D.B., Joullié, M.M., Ramotowski, R., and Cantu, A., Novel synthesis of thianinhydrin, Tetrahedron, 53, 4239, 1997. 124. Hauze, D.B., Petrovskaia, O., Joullié, M.M., and Hark, R.R., New reagents for the development of fingerprints, in Proc. Int. Symp. on Fingerprint Detection and Identification, Ne’urim, Israel, Almog, J. and Springer, E., Eds., Hemed Press, 1995, 119. 125. Frank, F.J., Borup, B., Brookman, J.A., Carr, A.J., Hurd, K.L., Renner, M., and Stowell, J.K., Preparation of ninhydrin analogs for fluorescent fingerprint development, poster presented at “Spectrum 91,” Int. Symp. Forensic Techniques, Detroit, Michigan, 1991. 126. Pounds, C.A., unpublished results (see Ref. 24). 127. Ohta, H., Suzuki, Y., Sugita, R., Suzuki, S., and Ogasawara, K., Examination of 5-alkoxyninhydrins as latent fingerprint visualization reagents, Can. Soc. Forensic Sci. J., submitted for publication, 2000. 128. Hark, R.R., Table of ninhydrin analogs, personal communication, Sept. 2000. 129. Almog, J., Sears, V.J., Springer, E., Hewlett, D.F., Walker, S., Wiesner, S., Lidor, R., and Bahar, E., Reagents for the chemical development of latent fingerprints: scope and limitations of benzo[ f ]ninhydrin in comparison to ninhydrin, J. Forensic Sci., 45, 538, 2000. 130. Hallman, J.L. and Bartsch, R.A., Synthesis of naphthoninhydrin, J. Org. Chem., 56, 6423, 1991. 131. Almog, J. and Springer, E., unpublished results, 1993.
132. Elber, R., Frank, A., and Almog, J., Chemical development of latent fingerprints: computational design of ninhydrin analogues, J. Forensic Sci., 45, 757, 2000. 133. Takatsu, M., Kageyama, H., Hirata, K., Akashi, T., Yoko Ta, T., Shiitani, M., and Kobayashi, A., Development of a new method to detect latent fingerprints on thermal paper with o-alkyl derivative of ninhydrin, Report of the National Institute of Police Science, Japan, 44, 1, 1991. 134. Grigg, R., Mongkolaussavaratana, T., Pounds, C.A., and Sivagnanam, S., 1,8-Diazafluorenone and related compounds. A new reagent for the detection of alpha amino acids and latent fingerprints, Tetrahedron Lett., 31, 7215, 1990. 135. Wilkinson, D., Study of the reaction mechanism of 1,8-diazafluoren-9-one with the amino acid L-alanine, Forensic Sci. Int., 109, 87, 2000. 136. Hardwick, S., Kent, T., Sears, V., and Winfield, P., Improvements to the formulation of DFO and the effects of heat on the reaction with latent fingerprints, Fingerprint Whorld, 19, 65, 1993. 137. Hewlett, D.F. and Sears, V.J., Formulation of amino acid reagents. Search for a safe effective replacement for CFCs, in Proc. Int. Symp. on Fingerprint Detection and Identification, Almog, J. and Springer, E., Eds., Ne’urim, Israel, 99, 1995. 138. Stoilovic, M., Improved method for DFO development of latent fingerprints, Forensic Sci. Int., 60, 141, 1993. 139. Margot, P. and Lennard, C., Fingerprint Detection Techniques, 6th revised edition, Université de Lausanne, 1994. 140. Geide, B., Detection of latent fingerprints — DFO without CFC, in Proc. Int. Symp. on Fingerprint Detection and Identification, Almog, J. and Springer, E., Eds., Ne’urim, Israel, 1995, 95. 141. Lennard, C., The effect of metal salt treatment on the photoluminescence of DFO-treated fingerprints, personal communication,1999. 142. Frank, F.J. and Handlin, N., Development of a latent fingerprint detection chemical: dibenzo-1,8-diazafluorenone, M.A.F.S. Newslett., 22, July 1993. 143. Frank, A., Grant, H., and Almog, J., Preliminary Tests on the Use of Two New Ketals of DFO for the Development of Latent Fingerprints, presented in a closed meeting on advances in fingerprint detection, PSDB, Home Office, U.K., 1996. 144. Ramotowski, R., Cantu, A.A., Joullié, M.M., and Petrovskaia, O.G., 1,2-Indanedione: a preliminary evaluation of a new class of amino acid visualizing compounds, Fingerprint Whorld, 23, 131, 1997. 145. Hauze, D.B., Petrovskaia, O.G., Taylor, B., Joullié, M.M., Ramotowski, R., and Cantu, A.A., 1,2-Indanediones: new reagents for visualizing the amino acid components of latent prints, J. Forensic Sci., 43, 744, 1998. 146. Almog, J., Springer, E., Wiesner, S., Frank, A., Khodzhaev, O., Lidor, R., Bahar, E., Varkony, H., Dayan, S., and Rozen, S., Latent fingerprint visualization by 1,2-indanedione and related compounds: preliminary results, J. Forensic Sci., 44, 114, 1999.
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Advances in Advances Fingerprint Te
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Advances in Fingerprint Technology
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Preface The first edition of this b
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Acknowledgments We gratefully ackno
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Table of Contents Preface Acknowled
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History and Development of Fingerpr
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Figure 1.2 Basic fingerprint patter
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Figure 1.3 Portion of the prehensil
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Figure 1.4 Elliptical whorl. Theory
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The bricks, carefully laid and accu
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the megalithic builders, including
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made most of them. These “identif
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Figure 1.6 Nehemiah Grew. (Drawn by
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Figure 1.7 Right palm imprint in pl
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By kindly words of persuasion a ref
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Loop: Now if this oblique stripe by
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Figure 1.11 Dr. Ivan Vucetich. (Dra
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Sir Edward Henry and Sir William He
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in charge he undoubtedly supported
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1. Finding finger imprints on prehi
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Faulds edited seven issues of a fin
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much of his inspired research. For
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to the unrelenting efforts of Steeg
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and gathered around him a nucleus o
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I find that portions of palm imprin
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Identification of Latent Prints ROB
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Without it, no amount of further la
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work will quite often fare badly un
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Figure 2.3 Polygon method. Overlay
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Experience and Skill Although the t
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The initial identification of the l
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D5 D6 D7 I2 D8 D9 D10 No No No Reco
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D11 I4 No D12 D11 I5 D12-1 D7 D12-2
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D14 I7 D16 C3 D11 D14-2 D7 D14-3 C2
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Figure 2.7 Example of pressure dist
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9. Mairs, G., Novel method of print
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DNA From Latent Prints DNA From Blo
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Figure 3.1 A schematic diagram show
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Figure 3.3 A schematic diagram of t
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(5 to 12 µg/L), bromide (0.2 to 0.
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electrophoresis (SDS-PAGE) include
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Table 3.3 Anatomical Variation in t
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Various oxidative and bacteriologic
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acid content can change with time i
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are of sebaceous origin. 82 Approxi
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Table 3.7 Changes in Surface Lipid
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gland’s activity. The more active
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content. 108 Palmitic acid was foun
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Figure 3.4a A chromatogram of a fin
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various lipid classes found in a la
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of DNA using RFLP. 130 No adverse e
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was later found to be caused by the
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17. Seutter, E., Goedhart-De Groot,
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52. Downing, D. T., Strauss, J. S.,
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85. Summerly, R., Yardley, H. J., R
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120. Duff, J. M. and Menzel, E. R.,
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149. Kloosterman, A., Application o
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Coumarin 540 Dye Staining Method An
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visualization of latent fingerprint
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White powder Dolomite, starch powde
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Fluorescein solution (in methanol/w
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Notes: Dissolve the MoS 2 in the di
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4. Avoid inhaling any iodine fumes
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CN CN CN A - A - CH2 C COOR CH2 C C
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Large vacuum chambers for processin
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Gentian Violet Solution — Non-Phe
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Table 4.1 Approximate Absorption an
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and recorded by autoradiography. Ni
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Ninhydrin solutions may be applied
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of development of ninhydrin-treated
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and certain nonreactive surface mat
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Procedure Xylene 50 mL Petroleum et
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ehavior of Ruhemann’s purple-meta
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4. Rinse the specimen in tap water.
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een treated with ninhydrin. In addi
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Working solution Stock solution 6 m
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Note: Combine and stir until citric
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Zauner 181 noted that on a rare occ
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3. Expose the tape surface to a hig
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lifting media were used, followed b
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under certain circumstances. The Br
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Physical Methods Visual Examination
Page 168 and 169: DRY Super Glue Fuming Powder Dustin
Page 170 and 171: Visual Examination Photography Iodi
Page 172 and 173: References 1. Olsen, R. D., Scott
Page 174 and 175: 36. Springer, E. and Bergman, P., A
Page 176 and 177: 74. McCarthy, M. M., Evaluation of
Page 178 and 179: 110. Mooney, D. G., Development of
Page 180 and 181: 142. Pounds, C. A., Grigg, R., and
Page 182 and 183: 175. Jones, R. J. and Pounds, C. A.
Page 184 and 185: 213. Hebrard, J. and Donche, A., Fi
Page 186 and 187: 245. Misner, A., Wilkinson, D., and
Page 188 and 189: Fingerprint Development by Ninhydri
Page 190 and 191: Figure 5.1 2,2-Dihydroxy-1,3-indane
Page 192 and 193: Figure 5.4 Formation of murexide (V
Page 194 and 195: Figure 5.6 The 1,3-dipole form of t
Page 196 and 197: less volatile 1,1,2-trichloroethane
Page 198 and 199: Key to Routes Primary Special Secon
Page 200 and 201: Specially designed cabinets for che
Page 202 and 203: the importance of cooling the objec
Page 204 and 205: Figure 5.10 Ninhydrin (I) and some
Page 206 and 207: een prepared and evaluated as finge
Page 208 and 209: Figure 5.14 The red pigment formed
Page 210 and 211: Figure 5.16 The fluorescent product
Page 212 and 213: 16. Pounds, C.A. and Jones, R.J., P
Page 214 and 215: 51. Jungbluth, W.O., Replacement fo
Page 216 and 217: 87. Kent, T., An operational guide
Page 220 and 221: 147. Dayan, S., Almog, J., Khodzhae
Page 222 and 223: Figure 6.1 Ninhydrin/ZnCl 2 vs. nin
Page 224 and 225: purposes of understanding their pho
Page 226 and 227: Ar-laser image monitor lens light c
Page 228 and 229: laser Figure 6.6 Block diagram of p
Page 230 and 231: step 1 step 2 step 3 fingerprint co
Page 232 and 233: nanocrystals. Photoluminescent semi
Page 234 and 235: Figure 6.11 Photoluminescence of fi
Page 236 and 237: H H H H N N CH2CH2 CH2CH2 H N N H N
Page 238 and 239: sample, rather than preferential ad
Page 240 and 241: O R C OH + R' NH2 R C Figure 6.16 G
Page 242 and 243: The amidation reaction depicted in
Page 248 and 249: R 1 - COOH + HO - N R 1 O C N H Fig
Page 250 and 251: 29. Sooklal, K., Hanus, L.H., Ploeh
Page 252 and 253: Procedure Water and Acid Pretreatme
Page 254 and 255: The Silver Physical Development Pro
Page 256 and 257: (in the emulsion) the silver and si
Page 258 and 259: ions (found only on paper that has
Page 260 and 261: as that of print residue on porous
Page 262 and 263: + + + + + + + Cit 3- Cit 3- Cit 3-
Page 264 and 265: Saunders. 22 Both workers recognize
Page 266 and 267: Figure 7.2 Scanning electron micros
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paper and these convert to ferric o
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Water and Acid Pretreatments The wa
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Figure 7.4 Comparison of a ninhydri
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Figure 7.7 Comparison of a ninhydri
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(0.2%) to not form silver oxide whe
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X-Ray and Scanning Electron Microsc
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is much to be done to optimize the
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3. Margot, P. and Lennard, C., Fing
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35. Morris, J.R. and Wells, J.M., A
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Introduction More than a century ha
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False Reject Rate (FRR) Civilian Ap
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Fingerprint Quality Acquisition Est
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finger gets mapped onto the two-dim
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(a) (b) (c) Figure 8.3 Fingerprint
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In forensics, a special kind of ink
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L A B (a) Finger Friction Surface R
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Fingerprint Representation A finger
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(a) (b) (c) (d) Figure 8.8 A finger
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Figure 8.10 Relative configuration
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A minutiae feature extractor finds
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depicting a ridge in the fingerprin
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1. Singular points. The Poincare in
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Table 8.2 shows the results of the
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(a) (b) Figure 8.13 Two different i
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ox size is adjusted based on the es
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(a) (b) Figure 8.16 Fingerprinting
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0.5 -0.5 -1 200 1 0.8 0.6 0.4 0.2 1
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andpass filters and extracts ridges
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(a) (b) Figure 8.19 Examples of enh
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A significant implication of the ab
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or otherwise. Therefore, there are
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Conclusions and Future Prospects Fi
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WSQ-related illustrations (Figure 8
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37. Siemens. The ID Mouse from Siem
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69. L. Hong, A. Jain, and S. Pankan
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Trauring Model (1963) Description o
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correspondence in friction ridge de
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extreme variability of friction rid
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5. Trauring 19 6. Kingston 20 7. Os
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variation need have no relationship
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1. Fork directed to the right 2. Fo
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e closer to reality. In any case, t
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There is not only opportunity for c
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that, in practice, it is relative d
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e the probability that there will b
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Correction factors (G) were introdu
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fingerprint individuality into two
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appreciated that the number of tria
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a corresponding reference point is
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Table 9.1 Kingston’s Relative Fre
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minutia counts in different-sized r
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If one is to use the compound forms
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Osterburg Model (1977-1980) Descrip
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of any occurrences that appear in t
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minutiae. Both the Kingston and Ost
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minutia orientation results in regi
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Orientation for minutiae was define
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the allowable combinations of minut
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selected for the study, based on th
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Table 9.4 Champod’s Upper Bound F
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that Champod and Margot proved to b
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fingerprint was isolated. This area
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that, for the experiments as design
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can be encouraged by the dedication
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37. Amy, L., Valeur de la preuve en
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The Expert Fingerprint Witness ROBE
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Qualifications of the Fingerprint E
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7. Results of comparisons conducted
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granted for a pretrial conference,
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any examination that I have conduct
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to fully understand the meaning of
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When seated in the witness stand, t
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jury but looked down at the floor i
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Courtroom Courtesy When in court, i
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If the attorney does not have the p
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Glossary of Commonly Used Courtroom
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Indictment An accusation in writing
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APPENDIX Daubert Hearings EDWARD GE
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The U.S. Government set presented e
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Presided over by the Honorable J. C
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