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ABSTRACT
INTRODUCTION
103
more variable in size and in frequency of various traits than their
more mesial neighbours (4). Since the classic studies of Butler
and Dahlberg there has been continuing and growing interest in
the patterns of odontogenic polarity and their application to Butler's
field theory. Although a large number of investigators have suggested
that their results are generally supportive of the field concept
(5 - 15), there are those who have questioned its validity (16 - 21).
Certainly the assumptions underlying the hypothesis seem questionable.
For example, Gingerich and Ryan (22) have shown that the second
molars in Indriidae are less variable that the first molars even
though they develop and erupt later. Also, using coefficients
of variation with sex influences removed (20), Kieser et al have
shown a reversal of the expected variability patterns inthe mesio-
distal dimensions of upper central and lateral incisors and the
buccolingual dimensions of the mandibular molars in Lengua Indians
(17). Interestingly, Harris and Nweeia (8) also reported a less
variable lateral upper incisor in the Ticuna Indians, a population
that showed an unusual lack of sexual dimorphism in tooth size.
On the basis of these findings it is argued that distal member
variability is not supportive of Butler's field theory as applied
to the human dentition.
Kollar and Lumsden (23) have divided odontogenesis into three main
phases: initiation, morphogenesis and cytodifferentiation. It
is a well documented fact that tooth development involves the inter-
action of neural crest derived ectomesenchyme and the oral epithelium
(24, 25). What the factos are that determine tooth size and shape
however, has been the subject of considerable dispute. Butler
(26, 27) has suggested that differences between the teeth within
a dentition reflect the reaction of ectomesenchymal cells to the
influence of fields into which these cells migrate. Osborn, on
the other hand, proposed a clonal model that views mesenchymal
cells as being predetermined by the time they enter the jaws (28).
In agreement with Osborn and with Schwartz (29), it is proposed
here that ectomesenchymal stem cells enter the presumptive jaws
already differentiated into incisor, canine and molar cell masses.
Rather than attributing the phenotypic variability of the tooth
to this position within a morphogenetic field, it is suggested that
variability may be attributable to the length of time that the
tooth spends in its soft tissue stage. Variability hence becomes
an epigenetic phenomenon, unrelated to field substance concentration.
EMPIRICAL SUPPORT
104
with their respective percentages of time spent in the soft tissue
stage, were plotted (Figure 1). Statistically significant levels
of Spearman's rank order correlation coefficient (rs maxilla = 0.78;
rs mandible = 0.61) allow one to conclude that there is in fact a
close correlation between time spent in the tissue stage and phenn-
typic variation of the end product.
CONCLUSION
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