Neuropsychologia 40 (2002) 1516–1522
Note
Sex and spatial position effects on object location memory following
intentional learning of object identities
Gerianne M. Alexander
a,∗
, Mark G. Packard
b
, Bradley S. Peterson
c
a
Yale Child Study Center, 230 South Frontage Road, New Haven, CT 06520, USA
b
Yale Department of Psychology, 2 Hillhouse Avenue, New Haven, CT 06520, USA
c
Department of Child and Adolescent Psychiatry, New York State Psychiatric Institute, College of Physicians and Surgeons,
ColumbiaUniversity, New York, NY, USA
Received 20 February 2001; received in revised form 29 October 2001; accepted 29 October 2001
Abstract
Memory for object location relative both to veridical center (left versus right visual hemispace) and to eccentricity (central versus
peripheral objects) was measured in 26 males and 25 females using the Silverman and Eals Location Memory Task. A subset of participants
(17 males and 13 females) also completed a measure of implicit learning, the mirror-tracing task. No sex differences were observed in
memory for object identities. Further, in both sexes, memory for object locations was better for peripherally located objects than for centrally
located objects. In contrast to these similarities in female and male task performance, females but not males showed better recovery of
object locations in the right compared to the left visual hemispace. Moreover, memory for object locations in the right hemispace was
associated with mirror-tracing performance in women but not in men. Together, these data suggest that the processing of object features and
object identification in the left cerebral hemisphere may include processing of spatial information that may contribute to superior object
location memory in females relative to males. © 2002 Elsevier Science Ltd. All rights reserved.
Keywords: Human evolution; Spatial ability; Gender; Cognition
1. Introduction
Sex differences in human spatial abilities are consistent
with the predictions of evolutionary theory and the hypothe-
sized social roles of early women and men [7,36]. If hunters
were predominantly male, then it is reasoned that selec-
tion pressures might contribute to spatial abilities in men
that enhance the hunt and capture of animals. If gatherers
were predominantly female, then similar selection pressures
might contribute to a female advantage on different spatial
tasks. The successful gathering of plant food, for example,
may require abilities to identify the shape and color of ed-
ible plants and to associate landmarks (e.g. a particular tree
or rock) with their locations. The adaptive significance of
sex-specific spatial abilities is consistent with the present
day male advantage in spatial navigation [11,30,35] and the
accurate aim of projectiles [41]. In addition, tasks developed
specifically to test the novel hypothesis of a female advan-
∗
Corresponding author. Tel.: +1-203-432-4671; fax: +1-203-432-7172.
E-mail address: gerianne.alexander-packard@yale.edu
(G.M. Alexander).
tage on other spatial tasks show that women and young girls
outperform men and young boys in their memory for objects
identities and their locations in a visual spatial array [7,36].
Research of visual and spatial processing suggests that
these present day sex-typed spatial abilities (e.g. spatial nav-
igation or locating objects in an array) may have distinct neu-
ral bases that evolved from the diverse processing require-
ments of hunting and gathering. The gathering of animal
food through hunting involves the identification of spatial
position and movement, whereas the gathering of plant food
involves identification of object features, including color. In
primates, the identification of objects and their locations is
accomplished by two functionally and anatomically distinct
pathways that ultimately project to the frontal cortex [19,38].
Object recognition and the identification of visual patterns
and colors are processed through the parvocellular pathway
(the “what” pathway), which proceeds ventrally from the vi-
sual cortex to the inferior temporal region. Spatial locations,
object movements, and global analyses of visual scenes are
processed through the magnocellular pathway (the “where”
pathway), which proceeds dorsally from the visual cortex to
the posterior parietal cortex.
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