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Post by djoser-xyyman on Oct 4, 2010 11:53:59 GMT -5
Body Proportions of Circumpolar Peoples as Evidenced From Skeletal Data: Ipiutak and Tigara (Point Hope) Versus Kodiak Island Inuit Trenton W. Holliday1* and Charles E. Hilton2 1Department of Anthropology, Tulane University, New Orleans, LA 70118 2Department of Anthropology, Grinnell College, Grinnell, IA 50112-1690 KEY WORDS Bergmann’s rule; Allen’s rule; ecogeographical patterning; cold adaptation ABSTRACT Given the well-documented fact that human body proportions covary with climate (presumably due to the action of selection), one would expect that the Ipiutak and Tigara Inuit samples from Point Hope, Alaska, would be characterized by an extremely coldadapted body shape. Comparison of the Point Hope Inuit samples to a large (n > 900) sample of European and European- derived, African and African-derived, and Native American skeletons (including Koniag Inuit from Kodiak Island, Alaska) confirms that the Point Hope Inuit evince a cold-adapted body form, but analyses also reveal some unexpected results. For example, one might suspect that the Point Hope samples would show a more cold-adapted body form than the Koniag, given their more extreme environment, but this is not the case. Additionally, univariate analyses seldom show the Inuit samples to be more cold-adapted in body shape than Europeans, and multivariate cluster analyses that include a myriad of body shape variables such as femoral head diameter, biiliac breadth, and limb segment lengths fail to effectively separate the Inuit samples from Europeans. In fact, in terms of body shape, the European and the Inuit samples tend to be cold-adapted and tend to be separated in multivariate space from the more tropically adapted Africans, especially those groups from south of the Sahara. Am J Phys Anthropol 142:287–302, 2010. VVC 2009 Wiley-Liss, Inc. Attachments:
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Post by djoser-xyyman on Oct 4, 2010 12:01:35 GMT -5
Relative Variation in Human Proximal and Distal Limb Segment Lengths Trenton W. Holliday1* and Christopher B. Ruff2 1Department of Anthropology, Tulane University, New Orleans, Louisiana 70118 2Department of Cell Biology and Anatomy, Johns Hopkins University Medical School, Baltimore, Maryland 21205 KEY WORDS limb proportions; allometry; variance-covariance matrices ABSTRACT The pattern of variation and covariation of proximal and distal limb segment lengths was examined within and between 20 geographically diverse skeletal samples of modern humans. Analyses of variance-covariance matrices (VCMs) of logarithmically transformed (ln) variates of humerus, radius, femur, and tibia length were performed to test the following hypotheses: first, within populations, the distal and proximal segments will have equal relative (i.e., size-independent) variability. However, between populations, the tibia is predicted to be more variable than the other segments. Tests of fit of computed VCMs to theoretical matrices by an iterative procedure (Anderson [1973] Ann. Stat. 1:135–141) reject the equal variance hypotheses, rather suggesting that the relative variances of the distal limb segments are greater than are those of the proximal. Males and females differ somewhat in that within females, the distal segments of both limbs have equal variance, while within males, the tibia has greater relative variance than the radius. The second hypothesis, regarding between-group variability, is somewhat supported in that between human populations, one cannot reject that the tibia has greater relative variance than the other limb segments. However, neither can one reject an alternative hypothesis that both distal limb segments (tibia and radius) are more variable than the proximal segments. Differential growth allometry is explored, and likely plays a major role in differences seen both within and between human populations. Am J Phys Anthropol 116:26 –33, 2001. © 2001 Wiley-Liss, Inc Attachments:
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Post by djoser-xyyman on Oct 6, 2010 10:38:55 GMT -5
One of the few interesting threads. So I will post.
What I got from the study is Europeans and other cold adapted peoples show similar traits. 1. Thick/long trunks 2. Short legs and arms 3. Large femoral indices 4. Broad hips(and flat butt). That why I can’t find a good pair of fitting jeans. LOL! 5. Hairy body What was the nonsense Gigantic was talking about “gracile” Europeans.
--------- From. . .
Body Proportions of Circumpolar Peoples as Evidenced From Skeletal Data: Ipiutak and Tigara (Point Hope) Versus Kodiak Island Inuit Trenton W. Holliday1* and Charles E. Hilton2 1Department of Anthropology, Tulane University, New Orleans, LA 70118 2Department of Anthropology, Grinnell College, Grinnell, IA 50112-1690
Rather, all high-latitude groups, including Europeans, evince a more cold-adapted physique, and only for a few key traits (e.g., relative bi-iliac breadth, female relative femoral head size) are the circumpolar groups consistently significantly more cold-adapted than Europeans. Thus, the major contrast in body shape is found between Europeans and circumpolar groups on the one hand, and tropical and, to a lesser extent, subtropical, Africans on the other.[/b] This is an [/b]unexpected finding [/b]in that it hints that[/b] Europeans likely experienced (and perhaps still experience today) significant selection for a ‘‘cold-adapted’’ postcranial morphology.[/b]
ABSTRACT Given the well-documented fact that human body proportions covary with climate (presumably due to the action of selection), one would expect that the Ipiutak and Tigara Inuit samples from Point Hope, Alaska, would be characterized by an extremely coldadapted body shape. Comparison of the Point Hope Inuit samples to a large (n > 900) sample of European and European- derived, African and African-derived, and Native American skeletons (including Koniag Inuit from Kodiak Island, Alaska) confirms that the Point Hope Inuit evince a cold-adapted body form, but analyses also reveal some unexpected results. For example, one might suspect that the Point Hope samples would show a more cold-adapted === body form than the Koniag, given their more extreme environment, but this is not the case. Additionally, univariate analyses seldom show the Inuit samples to be more cold-adapted in body shape than Europeans, and multivariate cluster analyses that include a myriad of body shape variables such as femoral head diameter, biiliac breadth, and limb segment lengths fail to effectively separate the Inuit samples from Europeans. In fact, in terms of body shape, the European and the Inuit samples tend to be cold-adapted and tend to be separated in multivariate space from the more tropically adapted Africans, especially those groups from south of the Sahara.[/b] Am J Phys Anthropol 142:287–302, 2010. V
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Archeological/artifactual evidence suggests that foragers in both periods exploited sea mammals (ocean currents keep much of the coastal water ice-free throughout the winter). However, during the Ipiutak Period, there was far more emphasis on caribou hunting, while during the later Tigara Period, hunters made much more frequent use of whales (Larsen and Rainey, 1948)—
=== Body proportions of humans [and other endothermic (i.e., ‘‘warm-blooded’’) species] have long been known to show significant correlations with climatic variables and their proxies.
==== Specifically, two empirically derived ecogeographical rules, those of Bergmann (1847) and Allen (1877), state that within a widespread endothermic species, those in colder regions will tend to weigh more (Bergmann’s rule) and be characterized by shorter appendages (Allen’s rule) than their conspecifics in warmer climes.
=== In particular, it has long been recognized that circumpolar peoples (e.g., Inuit, Aleuts, Sa´mi) have more foreshortened limb segments and broader trunks and are heavier on average than populations at even the mid-latitudes (Trinkaus, 1981; Ruff, 1994; Holliday, 1997b).
=== Note that while within each region, males tend to have higher indices than females; across regions, the Africans tend to have low index values and the circumpolar groups have high index values, with the Europeans appearing to be somewhat intermediate.
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Likewise, the North and Sub- Saharan African females are not significantly different from each other, but are different from all other groups European females are significantly different from all other groups, with significantly lower index values than the circumpolar groups and larger values than the African samples. Likewise, the European males have significantly smaller femoral heads than the Tigara and significantly larger femoral heads than the Africans.
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Two other indices studied are the brachial (radius length:humerus length) and crural (tibial length:femoral length) indices. These indices assess the length of the distal limb segment relative to its proximal counterpart within each limb and have long been known to exhibit a significant relationship with climatic variables, with groups from colder climes evincing lower ratios (Coon, 1962; Badoux, 1965; Trinkaus, 1981). This seems to be due to the fact that the length of the distal limb segment is more developmentally labile than the proximal segment (Jantz and Jantz, 1999; Holliday and Ruff, 2001).
=== As expected, the African groups have high brachial indices, while the European and circumpolar groups are characterized by lower indices.
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Box plots for the limb length:skeletal trunk height ratios are found in Figure 3A–D. All limb:trunk indices show an apparent clinal distribution, with European and circumpolar samples characterized by lower indices, while the Africans show higher index values.
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Note that the Nubians used in this study are thought by some to represent an immigrant population from Europe or Western Asia [see Holliday (1995)].
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Arctic Circle, we would find that they exhibit among the most extreme human body shapes in the world—i.e., they would be characterized by the most foreshortened limbs, the broadest pelves, and highest femoral head to femoral length ratios of all the groups sampled.
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The results of our study are somewhat mixed with regard to these hypotheses. As was found by Ruff (1994, 2002), contrasts between the circumpolar groups and Africans are consistently significant, with Ipiutak and Tigara males and females significantly different from the Sub-Saharan Africans for every calculated index, the Koniag different from the Sub-Saharan Africans for most indices, and all three circumpolar groups showing significant differences from the North Africans for a plurality, if not majority of the indices calculated. Contrasts between the circumpolar groups and the Europeans, however, are decidedly less marked.
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The environmental component of body proportions has been noted for some time in experimental studies (e.g., Lee et al., 1969; Weaver and Ingram, 1969; Riesenfeld, 1973) in which animals raised in different climate-controlled environments ultimately developed different body proportions, with animals raised in the cold evincing shorter limbs than their conspecifics (or litter mates) raised in hot environments.
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To make matters more complicated, climate is not the only factor that can act on body proportions—malnutrition is documented to lead to reduced stature, which tends to be associated with lower limb:trunk proportions and foreshortened distal limb segments (Tanner et al., 1982; Jantz and Jantz, 1999).
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Specifically, the earliest modern humans in Europe for whom we have body proportion data tend to show more African-like body proportions (Holliday, 1997a), while later European modern humans show foreshortened limbs in spite of archeological data indicative of improved cultural buffering. This suggests selection for shorter limbs in Late Pleistocene Europe, although we also cannot as of yet rule out the possibility that late Pleistocene gene flow from Neandertals to early modern Europeans played some role in establishing more ‘‘cold-adapted’’ limb proportions for this latter population (Holliday, 1997a, 2006b).
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and it is even more surprising that these three circumpolar groups exhibit so few body proportion differences from Europeans.
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