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Re: [Marxism] So it's not the opposable thumb, after all?
- To: Activists and scholars in Marxist tradition <marxism@xxxxxxxxxxxxxxxxxxx>
- Subject: Re: [Marxism] So it's not the opposable thumb, after all?
- From: Rod Holt <rholt@xxxxxxxxxxxxxx>
- Date: Sun, 21 Nov 2004 15:53:45 -0800
- User-agent: Mozilla/5.0 (Macintosh; U; PPC Mac OS X Mach-O; en-US; rv:1.4) Gecko/20030624 Netscape/7.1
Brian Shannon wrote:
News
Published online: 17 November 2004; | doi:10.1038/news041115-9
Distance running 'shaped human evolution'
Michael Hopkin
Our African ancestors may have been talented endurance athletes.
Long-distance running was crucial in creating our current upright body
form, according to a new theory.
(snip)
Although I am no expert, I found a substantial difference between the
article by Bramble and Lieberman and the one quoted from the same
magazine by Michael Hopkin.
Mike Friedman (11/18/04) was certainly correct to say, “I don't buy
the argument that long-distance running ‘was crucial in creating our
current upright body form.’” Fortunately, the excellent article by
Bramble and Lieberman did not make such a claim. Rather, they
presented anatomical evidence to show that the abilities of humans to
run rapidly for long distances should be included in any discussion of
human evolution. Throughout, they assume that pre-Homo genus all
walked exclusively upright.
The entire paper is well worth reading, particularly in light of the
articles on Homo floresiensis published 2 weeks earlier in Nature
(vol. 431, October 28, 2004).
The paper concerning endurance running is much too long to put in
Marxmail and the illustrations are essential. Since one needs to be a
subscriber to Nature to obtain the article on line, I present excerpts
below with footnotes, references and illustrations removed, and my
remarks in square brackets. I include the author’s last paragraph
which carries their perspective fairly enough. The body of the paper
is devoted to an extensive review of biomechanics, fossil evidence,
and an evaluation of other established evolutionary hypotheses.
-rod
Nature, vol. 432, pages 345 - 352 (18 November 2004)
Endurance running and the evolution of Homo
By Dennis M. Bramble and Daniel E. Lieberman
[Their first paragraphs.] Striding bipedalism is a key derived
behavior of hominids that possibly originated soon after the
divergence of the chimpanzee and human lineages. Although bipedal
gaits include walking and running, running is generally considered to
have played no major role in human evolution because humans, like
apes, are poor sprinters compared to most quadrupeds. Here we assess
how well humans perform at sustained long-distance running, and review
the physiological and anatomical bases of endurance running
capabilities in humans and other mammals. Judged by several criteria,
humans perform remarkably well at endurance running, thanks to a
diverse array of features, many of which leave traces in the skeleton.
The fossil evidence of these features suggests that endurance running
is a derived capability of the genus Homo, originating about 2 million
years ago, and may have been instrumental in the evolution of the
human body form.
Most research on the evolution of human locomotion has focused on
walking. There are a few indications that the earliest-known hominids
were bipeds, and there is abundant fossil evidence that
australopithecines habitually walked by at least 4.4 million years
(Myr) ago. Many researchers interpret the evolution of an essentially
modern human-like body shape, first apparent in early Homo erectus, as
evidence for improved walking performance in more open habitats that
came at the expense of retained adaptations in the australopithecine
postcranium for arboreal locomotion. Although the biomechanics of
running, the other human gait, is well studied, only a few researchers
have considered whether running was a mode of locomotion that
influenced human evolution. This lack of attention is largely because
humans are mediocre runners in several respects. Even elite human
sprinters are comparatively slow, capable of sustaining maximum speeds
of only 10.2 m s-1 [23 mph] for less than 15 s. In contrast, mammalian
cursorial specialists such as horses, greyhounds and pronghorn
antelopes can maintain maximum galloping speeds of 15–20 m s-1 [34-45
mph] for several minutes. Moreover, running is more costly for humans
than for most mammals, demanding roughly twice as much metabolic
energy per distance traveled than is typical for a mammal of equal
body mass. Finally, human runners are less maneuverable and lack many
structural modifications characteristic of most quadrupedal cursors
such as elongate digitigrade feet and short proximal limb segments.
However, although humans are comparatively poor sprinters, they also
engage in a different type of running, endurance running (ER), defined
as running many kilometers over extended time periods using aerobic
metabolism. Although not extensively studied in non-humans, ER is
unique to humans among primates, and uncommon among quadrupedal
mammals other than social carnivores (such as dogs and hyenas) and
migratory ungulates (such as wildebeest and horses). Here, we review
the evidence for and impact of ER in human evolution. We begin with a
discussion of the mechanical differences between walking and running,
and how well humans perform at ER compared to other mammals. We then
review what is known about the key structural specializations thought
to underlie human ER capabilities, the extent to which they may be
features that evolved originally for bipedal walking, and the evidence
for their appearance in the hominid fossil record. We conclude by
outlining some hypotheses for why ER capabilities initially arose in
the genus Homo, and the significance of this behavior for human
evolution.
--------
…Average ER speeds for recreational joggers range between 3.2–4.2 m
s-1 [9 mph].From an evolutionary perspective, it is important to note
that human ER speeds are exceptional compared to non-human primates.
Apes such as chimpanzees, and other primates, such as patas monkeys,
can sprint rapidly, but they do so rarely and only for short
distances. No primates other than humans are capable of ER.
… Human ER speeds exceed the preferred trotting (3.1 m s-1) and the
trot–gallop transition (4.4 m s-1) speeds of ponies (110–170 kg)
[240-375 lb.], and even the preferred trotting speed predicted for a
500-kg quadruped. … Most cursorial quadrupeds such as zebra,
antelopes, and African hunting dogs trot when running long distances, …
… human ER speeds are quite comparable to the preferred galloping
speeds that cursors use over longer distances and times. Minetti has
shown that sustainable galloping speeds in horses decline considerably
for runs longer than 10–15 min, accounting for the average daytime
speed of 5.8 m s-1 [13 mph] at which long-distance postal horses were
consistently run for millennia. Wildebeests ( 100 kg) prefer to canter
at 5.1 m s-1. Well-conditioned human runners exceed the predicted
preferred galloping speed for a 65-kg quadruped and can occasionally
outrun horses over the extremely long distances that constrain these
animals to optimal galloping speeds, typically a canter.
… This is not to say that humans can outdistance specialized
quadrupeds. Some horse and dog breeds, for example, can be made to run
more than 100 km day-1 while carrying or pulling a human. Such extreme
and human-induced feats, however, should not detract from the fact
that humans can and do run long distances well, despite a primate
ancestry.
--------
The ER capabilities of Homo raise several additional questions, the
first being whether long-distance running was an important behavior in
human evolution or merely the by-product of enhanced walking
capabilities. Traditional arguments have favored the latter
hypothesis; several of the derived features of Homo in Table 1 are
proposed as adaptations to improve long-distance walking performance
in more arid, open habitats. These features include relatively longer
legs, larger hindlimb and vertebral joint surfaces, narrower waists
and shorter toes. Yet walking alone cannot account for many of the
other derived features because the mass-spring mechanics of running,
which differ fundamentally from the pendular mechanics of walking,
require structural specializations for energy storage and
stabilization that have little role in walking. …
-------
Considering all the evidence together, it is reasonable to hypothesize
that Homo evolved to travel long distances by both walking and
running. New fossils and more detailed analyses of the existing fossil
record are needed to test whether these two locomotor capabilities
emerged concurrently or whether ER evolved after selection for
long-distance walking. An even more difficult task is to determine
what behaviors selected for ER in the first place. Why would early
Homo run long distances when walking is easier, safer and less costly?
One possibility is that ER played a role in helping hominids exploit
protein-rich resources such as meat, marrow and brain first evident in
the archaeological record at approximately 2.6 Myr ago, coincident
with the first appearance of Homo.
…
Additional research will help to clarify and test when and how ER
capabilities evolved in humans, and to examine more thoroughly their
implications for human evolution. For example, it is known that major
increases in encephalization occurred only after the appearance of
early Homo. The hypothesis that ER evolved in Homo for scavenging or
even hunting therefore suggests that ER may have made possible a diet
rich in fats and proteins thought to account for the unique human
combination of large bodies, small guts, big brains and small teeth.
--------
Correspondence and requests for materials should be addressed to
D.M.B. (bramble@xxxxxxxxxxxxxxxxxxx) or D.E.L. (danlieb@xxxxxxxxxxxxxxx).
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