Mw. Hamrick, FUNCTIONAL OSTEOLOGY OF THE PRIMATE CARPUS WITH SPECIAL REFERENCE TO STREPSIRHINI, American journal of physical anthropology, 104(1), 1997, pp. 105-116
Preuschoft et al. ([1993] in H. Preuschoft and D. Chivers (eds.): Hand
s of Primates. New York: Springer-Verlag, pp. 245-256) used a theoreti
cal biomechanical analysis to generate several predictions relating su
bordinal differences in primate hand proportions to differences in car
pal morphology. This study tests these predictions using quantitative
analyses of carpal morphology between extant haplorhine and strepsirhi
ne primates. Results show that living strepsirhines have a significant
ly larger hamate hamulus than do haplorhines, supporting Preuschoft et
al.'s (1993) predictions. Extant strepsirhines also have a significan
tly shorter pisiform body than do haplorhines and arboreal nonprimate
eutherians and a larger scaphoid tubercle than New and Old World monke
ys. These results contrast markedly with those expected under Preuscho
ft et al.'s (1993) model. Furthermore, strepsirhines and haplorhines d
o not differ significantly in the relative size of their radiocarpal a
rticulations. These morphometric observations do not match the predict
ed morphological patterns because the kinematic assumptions upon which
the biomechanical models are based are incorrect. Living strepsirhine
s appear to be derived in having very deep radial and ulnar margins of
the carpal tunnel for well-developed extrinsic digital flexors. Moreo
ver, tooth-combed prosimians differ from most haplorhines, early Terti
ary adapiforms, and arboreal nonprimate eutherians in having a relativ
ely short pisiform body, which gives the flexor carpi ulnaris less pow
er to flex the wrist from extended (= dorsiflexed) positions. These st
ructural observations suggest that powerful manual grasping and an emp
hasis on leaping and climbing, rather than palmigrade quadrupedal walk
ing and running, are morphotypic for extant Strepsirhini. (C) 1997 Wil
ey-Liss, Inc.