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Advances in Fingerprint Technology.pdf

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Orientation for m<strong>in</strong>utiae was def<strong>in</strong>ed <strong>in</strong> relation to the ridge flow by<br />

align<strong>in</strong>g ridges horizontally. If a m<strong>in</strong>utia produced an extra ridge as one<br />

followed the ridges from left to right, the orientation was termed “positive.”<br />

If a m<strong>in</strong>utia resulted <strong>in</strong> the loss of a ridge, the orientation was termed<br />

“negative.” The relative position of neighbor<strong>in</strong>g m<strong>in</strong>utiae was described<br />

us<strong>in</strong>g the two variables: the number of ridges separat<strong>in</strong>g the m<strong>in</strong>utiae (the<br />

ridge count) and the distance between the m<strong>in</strong>utiae along the ridge flow<br />

(distance).<br />

For the ridge counts, a convention was <strong>in</strong>troduced to accommodate<br />

m<strong>in</strong>utiae that occurred on the same ridge. This occurs, for example, when<br />

one branch of a fork term<strong>in</strong>ates. Either the upper or lower branch could<br />

term<strong>in</strong>ate, and either would have a ridge count of zero. Stoney and Thornton<br />

assigned either a “+0” or “–0” ridge count <strong>in</strong> these situations to describe the<br />

upper or lower relationship.<br />

The distance along the ridges was measured <strong>in</strong> units of ridge <strong>in</strong>tervals<br />

from one m<strong>in</strong>utia, along its ridge, until encounter<strong>in</strong>g a transect l<strong>in</strong>e runn<strong>in</strong>g<br />

from the second m<strong>in</strong>utia to the first m<strong>in</strong>utia’s ridge, perpendicularly across<br />

the ridge flow.<br />

Us<strong>in</strong>g this system, Stoney and Thornton concisely described neighbor<strong>in</strong>g<br />

m<strong>in</strong>utia pairs us<strong>in</strong>g six variables: the orientations of the two m<strong>in</strong>utiae, the<br />

types of the two m<strong>in</strong>utiae, the ridge count, and the distance. In all, 2645<br />

m<strong>in</strong>utia pairs were sampled.<br />

Statistical Analysis and F<strong>in</strong>d<strong>in</strong>gs<br />

Stoney and Thornton’s statistical analysis of the 2645 m<strong>in</strong>utia pairs revealed<br />

a number of significant f<strong>in</strong>d<strong>in</strong>gs, which they compared with the work of<br />

other <strong>in</strong>vestigators. They qualified their work, however, as strictly apply<strong>in</strong>g<br />

only to the epidermal ridges on the distal tips of the male thumb.<br />

General F<strong>in</strong>d<strong>in</strong>gs. The method of m<strong>in</strong>utia description was found to be<br />

acceptable to describe f<strong>in</strong>gerpr<strong>in</strong>t variation. Ridge densities (number of<br />

ridges per centimeter) were found to be <strong>in</strong> excellent agreement with earlier<br />

studies by K<strong>in</strong>gston 20 and Cumm<strong>in</strong>s, Wait, and McQuitty. 55<br />

M<strong>in</strong>utia densities were found to differ from those reported by K<strong>in</strong>gston, 20<br />

by Osterburg et al., 21 and Dankmeijer et al., 56 with the discrepancy attributed<br />

to differences <strong>in</strong> the size and location of sampl<strong>in</strong>g regions. The f<strong>in</strong>d<strong>in</strong>gs did<br />

support the generalization made by prior <strong>in</strong>vestigators that m<strong>in</strong>utia density<br />

varies significantly among different areas with<strong>in</strong> epidermal ridge patterns. In<br />

the distal region of the thumbpr<strong>in</strong>ts, however, no difference <strong>in</strong> m<strong>in</strong>utia<br />

density was seen among the various pattern types.

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