Investigating the case of human nose shape and climate adaptation
Open accessAbstract
The evolutionary reasons for variation in nose shape across human populations have been subject to continuing debate. An import function of the nose and nasal cavity is to condition inspired air before it reaches the lower respiratory tract. For this reason, it is thought the observed differences in nose shape among populations are not simply the result of genetic drift, but may be adaptations to climate. To address the question of whether local adaptation to climate is responsible for nose shape divergence across populations, we use Qst-Fst comparisons to show that nares width and alar base width are more differentiated across populations than expected under genetic drift alone. To test whether this differentiation is due to climate adaptation, we compared the spatial distribution of these variables with the global distribution of temperature, absolute humidity, and relative humidity. We find that width of the nares is correlated with temperature and absolute humidity, but not with relative humidity. We conclude that some aspects of nose shape may indeed have been driven by local adaptation to climate. However, we think that this is a simplified explanation of a very complex evolutionary history, which possibly also involved other non-neutral forces such as sexual selection.
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Written from the paper’s full text.
TL;DR
This study uses Qst–Fst comparisons and climate associations to test whether human nose shape divergence reflects local adaptation to climate. It finds nares width and alar base width exceed neutral expectations, and nares width correlates with temperature and absolute humidity, though the authors conclude climate adaptation is likely only part of a complex evolutionary history.
Key findings
- Nares width (Qst = 0.467, p = 2.80E-03) and alar base width (Qst = 0.440, p = 4.90E-03) show accelerated divergence across populations; skin pigmentation also does (Qst = 0.642, p = 1.00E-04), while height does not (Qst = 0.177, p = 0.1433).
- Nares width is significantly correlated with temperature (slope = 0.107, p = 2.37E-03) and absolute humidity (slope = 0.149, p = 6.97E-03), but not relative humidity (p = 0.100); alar base width is only mildly correlated with absolute humidity (p = 0.038).
- Skin pigmentation is strongly correlated with UVB (T = 6.23, LRT = 55.20, p = 1.09E-13), used as proof of principle.
- Nose shape traits are heritable in Europeans (hg2 range 0.401–0.657, N = 1,718), and between-population heritability estimates in Cape Verdeans include nares width hy2 = 0.226 and alar base width hy2 = 0.212 (N = 409).
Methods
- 3D facial images were captured with the 3dMD system; 7,150 quasi-landmarks were mapped, and 709 nose-region quasi-landmarks were used to compute five linear distances and two areas. Qst–Fst analyses used four population groups: West African (N = 40), North European (N = 236), East Asian (N = 127), and South Asian (N = 73).
- Qst–Fst comparisons used a non-parametric bootstrap with 10,000 pseudo-samples; Fst was estimated from 118,420 autosomal SNPs using Weir and Cockerham’s θ, and sensitivity to c/h2 assumptions was evaluated.
- Climate adaptation was tested in 140 females using linear mixed models correcting for age, BMI, and genetic similarity, with climate values from parents’ birthplaces; heritability was estimated with GCTA in 1,825 Europeans and with local ancestry in 409 Cape Verdeans.
Limitations
- The paper states that sampling of populations is sparse, higher-latitude sampling is limited, and results need replication in a larger set of populations; climate analyses used only females because genotype data were unavailable for males from Ireland and Poland.
- The paper notes that heritability estimates were limited to individuals with West African and European ancestry and do not reflect variation within and across other populations.
- The text makes evident that Qst inference depends on the c/h2 assumption, that the climate signal is weaker than for skin pigmentation, and that alternative non-neutral forces such as sexual selection remain speculative.
Model-written summary. Check it against the paper before relying on it.
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Claims the paper makes
0 of 66 cited sources checked · 0 supported · 0 flagged
- Findingown data
E. Asians tend to have the smallest noses in terms of external surface area.
“E. Asians also tend to have the smallest noses in terms of external surface area.”
Quote in the paperNot a substantial claim - Findingown data
Skin pigmentation shows a strong signal of accelerated divergence across populations (Qst = 0.642, p-value = 1.00E-04).
“As expected, skin pigmentation shows a strong signal of accelerated divergence across populations (Qst = 0.642, p-value = 1.00E-04).”
Quote in the paperNot a substantial claim- The authors state this as an assumption: The ratio c/h2 is equal to 1, i.e., the proportion of phenotypic variance due to additive genetic effects is the same among- and within-populations.
- Findingown data
Males tend to have bigger nostrils than females.
“Males, on average, tend to have wider nares, longer nasal ridges, more outwardly protruding nasal tips, bigger nostrils, and a larger overall external surface area, compared to females (Fig 2, Table 1).”
Quote in the paperNot a substantial claim - Findingown data
All nasal measurements are significantly different across populations.
“All nasal measurements are also significantly different across populations (S1 Table).”
Quote in the paperNot a substantial claim - Findingown data
Males tend to have longer nasal ridges than females.
“Males, on average, tend to have wider nares, longer nasal ridges, more outwardly protruding nasal tips, bigger nostrils, and a larger overall external surface area, compared to females (Fig 2, Table 1).”
Quote in the paperNot a substantial claim
- Findingown data
Males tend to have more outwardly protruding nasal tips than females.
“Males, on average, tend to have wider nares, longer nasal ridges, more outwardly protruding nasal tips, bigger nostrils, and a larger overall external surface area, compared to females (Fig 2, Table 1).”
Quote in the paperNot a substantial claim - Findingown data
All aspects of nose shape considered in the study are highly sexually dimorphic.
“One clear observation is that all aspects of nose shape, at least those considered here, are highly sexually dimorphic (Fig 2, Table 1).”
Quote in the paperNot a substantial claim - Findingown data
Males tend to have wider nares than females.
“Males, on average, tend to have wider nares, longer nasal ridges, more outwardly protruding nasal tips, bigger nostrils, and a larger overall external surface area, compared to females (Fig 2, Table 1).”
Quote in the paperNot a substantial claim - Findingown data
Nares width and alar base width are more differentiated across human populations than expected under genetic drift alone.
“we use Qst–Fst comparisons to show that nares width and alar base width are more differentiated across populations than expected under genetic drift alone.”
- Also stated in: § Testing for accelerated divergence · plain
“Of all the nose shape measurements, only nares width (Qst = 0.467, p-value = 2.80E-03) and alar base width (Qst = 0.440, p-value = 4.90E-03) exhibit signals of accelerated divergence.”
Quote in the paperSubstantial claim- The authors state this as an assumption: The ratio c/h2 is equal to 1, i.e., the proportion of phenotypic variance due to additive genetic effects is the same among- and within-populations.
- Also stated in: § Testing for accelerated divergence · plain
- Findingown data
Males tend to have a larger overall external surface area of the nose than females.
“Males, on average, tend to have wider nares, longer nasal ridges, more outwardly protruding nasal tips, bigger nostrils, and a larger overall external surface area, compared to females (Fig 2, Table 1).”
Quote in the paperNot a substantial claim - Findingown data
The degree of divergence in nares width and alar base width is not as high as that observed for skin pigmentation.
“However, the degree of divergence in these traits is not as high as that observed for skin pigmentation.”
Quote in the paperNot a substantial claim- The authors state this as an assumption: The ratio c/h2 is equal to 1, i.e., the proportion of phenotypic variance due to additive genetic effects is the same among- and within-populations.
- Findingown data
The 95% confidence intervals of the phenotype-climate slopes overlap with zero only when Northern Europeans are removed.
“Fig 7 shows that the 95% confidence intervals of the slope overlap with zero (red line in Fig 7) only when the N. Europeans are removed”
Quote in the paperSubstantial claim- Rests on an assumption: The climate at the parents' birthplaces is a good proxy for the individual's ancestral climate.
- Findingown data
Almost all aspects of nose shape seem to be highly heritable in Europeans (hg2 range: 0.401-0.657, N = 1,718).
“Almost all aspects of nose shape seem to be highly heritable in Europeans (hg2 range: 0.401–0.657 N = 1,718) (Table 3).”
Quote in the paperSubstantial claim - Findingown data
Nares width is not significantly correlated with relative humidity (N = 140, T = -1.65, LRT = 2.71, p = 0.100).
“Nares width was not significantly correlated with relative humidity (N = 140, T = -1.65, LRT = 2.71, p-value = 0.100).”
Quote in the paperNot a substantial claim- Rests on an assumption: The climate at the parents' birthplaces is a good proxy for the individual's ancestral climate.
- Findingown data
The correlation between skin pigmentation and UVB is positive, with people tending to be darker in regions with higher UVB exposure and vice versa.
“The positive values of the slope and t-statistic indicate that people tend to be darker in regions with higher exposure to UVB and vice versa.”
Quote in the paperSubstantial claim - Findingown data
Nares width is significantly correlated with absolute humidity (N = 140, T = 2.73, LRT = 7.28, p = 6.97E-03).
“Nares width is significantly correlated with temperature (N = 140, T = 3.09, LRT = 9.24, p-value = 2.37E-03) and absolute humidity (N = 140, T = 2.73, LRT = 7.28, p-value = 6.97E-03).”
Quote in the paperSubstantial claim- Rests on an assumption: The climate at the parents' birthplaces is a good proxy for the individual's ancestral climate.
- Findingown data
Skin pigmentation is strongly correlated with UVB exposure (N = 126, T = 6.23, LRT = 55.20, p = 1.09E-13).
“As expected, we see a strong relationship between skin pigmentation and UVB (N = 126, T = 6.23, LRT = 55.20, p-value = 1.09E-13).”
Quote in the paperNot a substantial claim - Findingown data
Nares width is significantly correlated with mean annual temperature (N = 140, T = 3.09, LRT = 9.24, p = 2.37E-03).
“Nares width is significantly correlated with temperature (N = 140, T = 3.09, LRT = 9.24, p-value = 2.37E-03) and absolute humidity (N = 140, T = 2.73, LRT = 7.28, p-value = 6.97E-03).”
Quote in the paperSubstantial claim- Rests on an assumption: The climate at the parents' birthplaces is a good proxy for the individual's ancestral climate.
- Findingown data
Other aspects of nose shape may not be as heritable between W. Africans and Europeans (Nasal height: hy2 = 0.03, hy2 = 0.059, N = 409).
“Other aspects of nose shape may not be as heritable between these two populations (Nasal height: hy2 = 0.03, hy2 = 0.059, N = 409).”
Quote in the paperNot a substantial claim - Findingreasoning
The heritability of skin pigmentation is very low in Europeans (hg2 = 0.191; N = 1,231).
“Interestingly, the heritability of skin pigmentation is very low in Europeans (hg2 = 0.191; N = 1,231), which we think can be explained by reduced genetic variation at skin pigmentation loci due to strong positive selection for lighter skin in Europeans [17,21,38].”
Quote in the paperNot a substantial claim - Findingown data
Differences in many aspects of nose shape are heritable between W. Africans and Europeans (Nares width: hy2 = 0.226, Alar base width: hy2 = 0.212, Nasal tip protrusion: 0.177, External surface area: hy2 = 0.121, N = 409).
“Differences in many aspects of nose shape are also heritable (Nares width: hy2 = 0.226, Alar base width: hy2 = 0.212, Nasal tip protrusion: 0.177, External surface area: hy2 = 0.121, N = 409).”
Quote in the paperSubstantial claim - Findingown data
The phenotypic variation between W. Africans and Europeans in height is quite heritable (hy2 = 0.224, N = 409).
“Table 3 shows that the phenotypic variation between W. Africans and Europeans in height (hy2 = 0.224, N = 409) is quite heritable.”
Quote in the paperNot a substantial claim - Findingown data
Estimates of hy2 are generally lower than estimates of hg2 for all traits.
“Another interesting observation from Table 3 is that estimates of hy2 are generally lower than estimates of hg2 for all traits.”
Quote in the paperSubstantial claim - Findingown data
Height does not show signals of accelerated divergence across the populations considered (Qst = 0.177, p-value = 0.14).
“Height, on the other hand, does not show signals of accelerated divergence (Qst = 0.177, p-value = 0.14).”
- Also stated in: § Testing for accelerated divergence · hedged
“While height seems to be under positive selection within European and African populations separately [19,34], it does not appear to be driven by divergent selection pressures across the populations considered here.”
Quote in the paperNot a substantial claim- The authors state this as an assumption: The ratio c/h2 is equal to 1, i.e., the proportion of phenotypic variance due to additive genetic effects is the same among- and within-populations.
- Also stated in: § Testing for accelerated divergence · hedged
- Findingown data
The divergence in the width of the nares and alar base deviates from neutral expectations.
“We found that the divergence in the width of the nares and alar base deviate from neutral expectations”
Quote in the paperSubstantial claim- The authors state this as an assumption: Within-population heritability equals among-population heritability (c = h2) when calculating Qst from phenotype data.
- Findingown data
The critical value of c/h2 for alar base width is 0.55.
“The critical value of nares width is 0.50 and that of alar base width is 0.55, which are also much lower than 1 (Fig 4 and Table 2).”
Quote in the paperSubstantial claim- The authors state this as an assumption: The ratio c/h2 is equal to 1, i.e., the proportion of phenotypic variance due to additive genetic effects is the same among- and within-populations.
- Findingown data
The critical value of c/h2 for nares width is 0.50.
“The critical value of nares width is 0.50 and that of alar base width is 0.55, which are also much lower than 1 (Fig 4 and Table 2).”
Quote in the paperSubstantial claim- The authors state this as an assumption: The ratio c/h2 is equal to 1, i.e., the proportion of phenotypic variance due to additive genetic effects is the same among- and within-populations.
- Findingown data
This concordance is evident by comparing the mean measurements between Observer1 and Observer2.
“This concordance is evident by comparing the mean measurements between Observer1 and Observer2 (S6 Fig)”
Quote in the paperNot a substantial claim - Findingnone given
The signal of climate adaptation is not very strong, especially compared to skin pigmentation.
“we note that the signal of climate adaptation is not very strong, especially when compared to skin pigmentation.”
Quote in the paperSubstantial claim- Rests on an assumption: The climate at the parents' birthplaces is a good proxy for the individual's ancestral climate.
- Findingown data
Averaging local ancestry across all SNPs yields an estimate of global ancestry that is highly correlated with estimates obtained from ADMIXTURE using k = 2 (r2 ∼ 1).
“Averaging local ancestry across all SNPs yields an estimate of global ancestry that is highly correlated with estimates obtained from ADMIXTURE using k = 2 (r2 ∼ 1) (S4 Fig).”
Quote in the paperNot a substantial claim - Findingnone given
Nostril area does not show unusually high differentiation across populations.
“However, we note that nostril area does not show unusually high differentiation across populations”
Quote in the paperSubstantial claim - Findingown data
The error distribution for nostril area was similar for both Observer1 (95% CI: 0.914-1.930) and Observer2 (95% CI: 0.888-2.243).
“The error distribution for nostril area was similar for both Observer1 (95% CI: 0.914–1.930) and Observer2 (95% CI: 0.888–2.243).”
Quote in the paperNot a substantial claim - Premisecitation
There is substantial nose shape variation among human populations, in both the external morphology of the nose and the underlying cranial morphology.
“We know there is substantial nose shape variation among human populations, in both the external morphology of the nose as well as the underlying cranial morphology [1,2,9].”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [1] LG Farkas, 1986, Geography of the nose: a morphometric study, Aesthetic Plast Surg source
Not checked in the free run.
- cites [2] RG Franciscus, 1991, Variation in human nasal height and breadth, Am J Phys Anthropol source
Not checked in the free run.
- cites [9] CC Roseman, 2004, Multivariate apportionment of global human craniometric diversity, Am J Phys Anthropol source
Not checked in the free run.
- Interpretationown data
Some aspects of nose shape may have been driven by local adaptation to climate.
“We conclude that some aspects of nose shape may indeed have been driven by local adaptation to climate.”
Quote in the paperSubstantial claim - Premisecitation
A vital function of the nose is to warm inspired air to core body temperature and saturate it with water vapor before it reaches the lower respiratory tract.
“A vital function of the nose is to warm inspired air to core body temperature and saturate it with water vapor before it reaches the lower respiratory tract [3].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [3] VE Negus, 1954, Introduction to the comparative anatomy of the nose and paranasal sinuses, Ann R Coll Surg Engl
Not checked in the free run.
- Interpretationown data
Differences in skin pigmentation across continental populations have been driven by positive selection.
“This is in accordance with the idea that differences in skin pigmentation, at least across continental populations, have been driven by positive selection.”
Quote in the paperNot a substantial claim - Premisecitation
The nasal index varies significantly among populations.
“The nasal index (width/height of the nasal aperture of the skull) is also known to vary significantly among populations [1,2].”
Quote in the paperSubstantial claim0 of 2 sources checked - Premisecitation
The Qst of a neutrally evolving trait is expected to follow the Fst distribution of neutrally evolving loci.
“In principle, the Qst of a neutrally evolving trait is expected to follow the Fst distribution of neutrally evolving loci [11].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [11] MC Whitlock, 2009, Testing for spatially divergent selection: comparing QST to FST, Genetics source
Not checked in the free run.
- Premisecitation
The distance between the nasal alare is significantly larger in individuals of West African, South Asian, and East Asian ancestry compared to persons with European ancestry.
“For example, the distance between the nasal alare (wings of the nose) are significantly larger in individuals of West African, South Asian, and East Asian ancestry as compared to persons with European ancestry [1].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [1] LG Farkas, 1986, Geography of the nose: a morphometric study, Aesthetic Plast Surg source
Not checked in the free run.
- Premisecitation
Qst calculated from phenotype data assuming c = h2 is probably best considered the 'minimum' Qst proposed by Relethford (1994).
“Qst calculated this way is probably best considered to be the ‘minimum’ Qst proposed by Relethford (1994) [35].”
Quote in the paperSubstantial claim0 of 2 sources checked- cites Relethford (1994) source
Not checked in the free run.
- cites [35] JH Relethford, 1994, Craniometric variation among modern human populations, Am J Phys Anthropol source
Not checked in the free run.
- The authors state this as an assumption: Within-population heritability equals among-population heritability (c = h2) when calculating Qst from phenotype data.
- Study design and conductnone given
The results that nares width and alar base width deviate from neutral expectations are robust to the c = h2 assumption.
“and that these results are robust to the c = h2 assumption.”
Quote in the paperSubstantial claim- The authors state this as an assumption: Within-population heritability equals among-population heritability (c = h2) when calculating Qst from phenotype data.
- Premisecitation
Previous Qst-based studies of craniofacial divergence assumed h2 = 0.55 and c = 1, resulting in c/h2 greater than 1.
“In these studies, h2 was assumed to be 0.55 and c was implicitly assumed to be 1, resulting in c/h2 to be greater than 1.”
Quote in the paperSubstantial claim0 of 4 sources checked- cites [12] CC Roseman, 2004, Detecting interregionally diversifying natural selection on modern human cranial form by using matched molecular and morphometric data, Proc Natl Acad Sci U S A source
Not checked in the free run.
- cites [13] M Hubbe, 2009, Climate signatures in the morphological differentiation of worldwide modern human populations, Anat Rec source
Not checked in the free run.
- cites [14] J Guo, 2014, Variation and signatures of selection on the human face, J Hum Evol source
Not checked in the free run.
- cites [35] JH Relethford, 1994, Craniometric variation among modern human populations, Am J Phys Anthropol source
Not checked in the free run.
- Interpretationown data
The width of the nares and alar base may have evolved across populations due to divergent selection.
“This suggests that the width of the nares and alar base may have evolved across populations due to divergent selection.”
Quote in the paperSubstantial claim- The authors state this as an assumption: Within-population heritability equals among-population heritability (c = h2) when calculating Qst from phenotype data.
- Interpretationown data
The skin pigmentation-UVB pattern provides further support that adaptation to ultraviolet radiation has had an important role in the evolution of skin pigmentation in humans.
“This pattern provides further support to the notion that adaptation to ultraviolet radiation has had an important role in the evolution of skin pigmentation in humans.”
Quote in the paperNot a substantial claim - Interpretationreasoning
The proportion of phenotypic variance in an admixed population that can be explained by local ancestry (hy2) is conceptually equivalent to c between the parental populations.
“The proportion of phenotypic variance in an admixed population that can be explained by local ancestry (hy2) is conceptually equivalent to c between the parental populations.”
Quote in the paperSubstantial claim - Interpretationreasoning
The strength of selection exerted by temperature on nose width is likely much weaker than the selection pressure imposed by UVB exposure on skin pigmentation.
“However, even nares width is not as strongly correlated with temperature and humidity as skin pigmentation is to UVB, suggesting that the strength of selection exerted by temperature on nose width is likely to be much weaker than the selection pressure imposed by UVB exposure on skin pigmentation.”
Quote in the paperSubstantial claim- Rests on an assumption: The climate at the parents' birthplaces is a good proxy for the individual's ancestral climate.
- Interpretationreasoning
For most human traits, the additive genetic variance between populations might be less than the additive genetic variance within populations.
“This suggests that for most human traits, the additive genetic variance between populations might be less than the additive genetic variance within populations, which agrees with the fact that most of the genetic variation in humans exists within populations.”
Quote in the paperSubstantial claim- Rests on an assumption: Most genetic variation in humans exists within populations.
- Study design and conductown data
The sampling of populations at higher latitude is limited and sparse, which is a limitation of this study.
“However, because our sampling of populations at higher latitude is limited (Fig 6), this result requires further investigation.”
- Also stated in: § Discussion · plain
“but also due the sparse sampling of populations shown here, which is a limitation of this study.”
Quote in the paperSubstantial claim - Also stated in: § Discussion · plain
- Premisecitation
The geometry of the nose is important for its respiratory functions.
“Computational fluid dynamics (CFD) studies show that the geometry of the nose is important for its respiratory functions [5,44].”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [5] S Naftali, 2005, The Air-Conditioning Capacity of the Human Nose, Ann Biomed Eng source
Not checked in the free run.
- cites [44] T Keck, 2010, Numerical simulation and nasal air-conditioning, GMS Curr Top Otorhinolaryngol Head Neck Surg
Not checked in the free run.
- Interpretationown data
The signal of climate adaptation might be specific to the width of the nares rather than the width of the nose per se.
“This might suggest that it is not the width of the nose per se but the width of the nares that is under selection pressure.”
Quote in the paperSubstantial claim- Rests on an assumption: The climate at the parents' birthplaces is a good proxy for the individual's ancestral climate.
- Premisecitation
The notion that Qst takes the minimum value relies on h2 always being less than c, which is anticonservative.
“However, the notion that this takes the minimum value of Qst relies on h2 always being less than c, which is anticonservative as has been noted previously [32].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [32] JE Brommer, 2011, Whither Pst? The approximation of Qst by Pst in evolutionary and conservation biology, J Evol Biol source
Not checked in the free run.
- The authors state this as an assumption: Within-population heritability equals among-population heritability (c = h2) when calculating Qst from phenotype data.
- Interpretationcitation
The low heritability of skin pigmentation in Europeans can be explained by reduced genetic variation at skin pigmentation loci due to strong positive selection for lighter skin in Europeans.
“Interestingly, the heritability of skin pigmentation is very low in Europeans (hg2 = 0.191; N = 1,231), which we think can be explained by reduced genetic variation at skin pigmentation loci due to strong positive selection for lighter skin in Europeans [17,21,38].”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [17] S Beleza, 2013, Genetic architecture of skin and eye color in an African-European admixed population. Spritz RA, editor, PLoS Genet source
Not checked in the free run.
- cites [21] RL Lamason, 2005, SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans, Science source
Not checked in the free run.
- cites [38] PC Sabeti, 2007, Genome-wide detection and characterization of positive selection in human populations, Nature source
Not checked in the free run.
- Interpretationown data
Genetic differences underlie the variation in many aspects of nose shape, both within- and between-populations.
“Altogether, our results show that genetic differences underlie the variation in many aspects of nose shape, both within- and between-populations.”
Quote in the paperSubstantial claim - Premisecitation
Absolute humidity is more important for the physiological functioning of the nose than relative humidity.
“This is not surprising since absolute humidity is more important for the physiological functioning of the nose than relative humidity [43].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [43] SD Maddux, 2016, Absolute humidity and the human nose: A reanalysis of climate zones and their influence on nasal form and function, Am J Phys Anthropol source
Not checked in the free run.
- Interpretationreasoning
Nares width and alar base width would exhibit signals of accelerated divergence even if the true values of c/h2 were much less than 1.
“Thus, we expect that these phenotypes would exhibit signals of accelerated divergence, even if the true values of c/h2 were much less than 1.”
Quote in the paperSubstantial claim- The authors state this as an assumption: The ratio c/h2 is equal to 1, i.e., the proportion of phenotypic variance due to additive genetic effects is the same among- and within-populations.
- Interpretationown data
Our findings provide support for the idea that differences in aspects of nose shape may have evolved across populations as a result of climate-related selection pressures.
“While our findings provide support for the idea that differences in aspects of nose shape may have evolved across populations as a result of climate-related selection pressures, something that has been demonstrated previously using craniometric data [2,12,13,41,42]”
Quote in the paperSubstantial claim0 of 5 sources checked- cites [2] RG Franciscus, 1991, Variation in human nasal height and breadth, Am J Phys Anthropol source
Not checked in the free run.
- cites [12] CC Roseman, 2004, Detecting interregionally diversifying natural selection on modern human cranial form by using matched molecular and morphometric data, Proc Natl Acad Sci U S A source
Not checked in the free run.
- cites [13] M Hubbe, 2009, Climate signatures in the morphological differentiation of worldwide modern human populations, Anat Rec source
Not checked in the free run.
- cites [41] TR Yokley, 2009, Ecogeographic variation in human nasal passages, Am J Phys Anthropol source
Not checked in the free run.
- cites [42] ML Noback, 2011, Climate-related variation of the human nasal cavity, Am J Phys Anthropol source
Not checked in the free run.
- Rests on an assumption: The climate at the parents' birthplaces is a good proxy for the individual's ancestral climate.
- The authors state this as an assumption: Within-population heritability equals among-population heritability (c = h2) when calculating Qst from phenotype data.
- Interpretationown data
Climate may not have been the only factor contributing to nose shape differences across populations.
“Climate may not have been the only factor in contributing to nose shape differences across populations.”
Quote in the paperSubstantial claim- Rests on an assumption: The climate at the parents' birthplaces is a good proxy for the individual's ancestral climate.
- Interpretationown data
It is not the size of the nostrils but the shape that might be functionally important.
“which suggests that it is not the size of the nostrils but the shape that might be functionally important.”
Quote in the paperSubstantial claim - Premisecitation
The geometry of the nasal airways influences the velocity of inspired air.
“We also know that the geometry of the nasal airways influences the velocity of inspired air [4,7,45].”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [4] LM Hanna, 1986, A Theoretical Model of Localized Heat and Water Vapor Transport in the Human Respiratory Tract, J Biomech Eng source
Not checked in the free run.
- cites [7] SE Churchill, 2004, Morphological variation and airflow dynamics in the human nose, Am J Hum Biol source
Not checked in the free run.
- cites [45] K Inthavong, 2007, CFD Simulations on the Heating Capability in a Human Nasal Cavity, Rhinology
Not checked in the free run.
- May combine two claims. 28
- Classified as probably not a substantial claim. 29
May combine two claims.
Findingown dataNares width is largest in W. Africans and smallest in N. Europeans.
“For example, nares width and alar base width are largest in W. Africans and smallest in N. Europeans.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataWidth of the nares is correlated with temperature and absolute humidity, but not with relative humidity.
“We find that width of the nares is correlated with temperature and absolute humidity, but not with relative humidity.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataAlar base width is largest in W. Africans and smallest in N. Europeans.
“For example, nares width and alar base width are largest in W. Africans and smallest in N. Europeans.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataNasal tip protrusion is greatest in N. Europeans and smallest in W. Africans and E. Asians.
“Nasal tip protrusion is greatest in N. Europeans and smallest in W. Africans and E. Asians.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThe positive slopes for nares width indicate that individuals from warm-humid climates tend to have wider nares, while individuals from cool-dry climates tend to have narrower nares.
“The positive slopes indicate that individuals from warm-humid climates, on average, tend to have wider nares whereas individuals from cool-dry climates tend to have narrower nares.”
Quote in the paperSubstantial claim- Rests on an assumption: The climate at the parents' birthplaces is a good proxy for the individual's ancestral climate.
May combine two claims.
Findingnone givenBoth within- and between-population variation in nose shape are heritable.
“In addition, we demonstrate that both within- and between-population variation in nose shape are heritable.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
FindingcitationThe heritability for height in Europeans (hg2 = 0.394; N = 1,825) is similar to previously reported estimates.
“The heritability for height in Europeans (hg2 = 0.394; N = 1,825) is similar to previously reported estimates [18].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [18] J Yang, 2010, Common SNPs explain a large proportion of the heritability for human height, Nat Genet source
Not checked in the free run.
May combine two claims.
Findingown dataSkin pigmentation has a critical value of c/h2 of 0.25, much lower than 1.
“Skin pigmentation, which shows a very high Qst value, has a critical value of 0.25, which is much lower than 1 (Fig 4 and Table 2).”
Quote in the paperSubstantial claim- The authors state this as an assumption: The ratio c/h2 is equal to 1, i.e., the proportion of phenotypic variance due to additive genetic effects is the same among- and within-populations.
Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Findingnone givenAll aspects of nose shape studied here are sexually dimorphic.
“We mentioned earlier that all aspects of nose shape studied here are sexually dimorphic”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataThe measurements from Observer2 are slightly more internally consistent than Observer1.
“The measurements from Observer2 are slightly more internally consistent than Observer1.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataBoth parents usually come from nearby regions, at least on a continental scale, and the climate values for the parents are quite similar.
“Both parents usually come from nearby regions, at least on a continental scale (Fig 6), and the climate values for the parents are quite similar (S5 Fig).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataFor Observer1, nasal tip protrusion was the least precise distance measure with 95% of the standard deviations falling between 0.791mm and 1.165mm, with error for the remaining distances well under 1mm.
“For Observer1, nasal tip protrusion was the least precise distance measure with 95% of the standard deviations falling between 0.791mm and 1.165mm, with error for the remaining distances well under 1mm.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataWith the exception of nasal tip protrusion (ICC = 0.819), the ICCs for all other measures were quite high (ICC > 0.95).
“With the exception of nasal tip protrusion (ICC = 0.819), the ICCs for all other measures were quite high (ICC > 0.95).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataTemperature is only weakly correlated with nares width, especially compared with the correlation between skin pigmentation and UVB.
“In fact, we show that temperature is only weakly correlated with nares width, especially when compared with the correlation between skin pigmentation and UVB.”
Quote in the paperSubstantial claim- Rests on an assumption: The climate at the parents' birthplaces is a good proxy for the individual's ancestral climate.
Classified as probably not a substantial claim. May combine two claims.
PremisecitationSeveral studies have found that most aspects of the skull seem to be evolving neutrally, while the shape of the nasal aperture appears to be more differentiated across human populations than expected under genetic drift.
“Several studies have used this approach and found that while most aspects of the skull seem to be evolving neutrally, the shape of the nasal aperture appears to be more differentiated across human populations than expected under genetic drift [9,12,13].”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [9] CC Roseman, 2004, Multivariate apportionment of global human craniometric diversity, Am J Phys Anthropol source
Not checked in the free run.
- cites [12] CC Roseman, 2004, Detecting interregionally diversifying natural selection on modern human cranial form by using matched molecular and morphometric data, Proc Natl Acad Sci U S A source
Not checked in the free run.
- cites [13] M Hubbe, 2009, Climate signatures in the morphological differentiation of worldwide modern human populations, Anat Rec source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationBoth height and skin pigmentation exhibit substantial variation within and across human populations, and are thought to be under positive selection in various populations.
“Both height and skin pigmentation exhibit substantial variation within and across human populations, and are thought to be under positive selection in various populations [19–22].”
Quote in the paperNot a substantial claim0 of 4 sources checked- cites [19] MC Turchin, 2012, Evidence of widespread selection on standing variation in Europe at height-associated SNPs, Nat Genet source
Not checked in the free run.
- cites [20] NG Jablonski, 2004, the Evolution of Human Skin and Skin Color, Annu Rev Anthropol source
Not checked in the free run.
- cites [21] RL Lamason, 2005, SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans, Science source
Not checked in the free run.
- cites [22] HL Norton, 2007, Genetic evidence for the convergent evolution of light skin in Europeans and East Asians, Mol Biol Evol source
Not checked in the free run.
May combine two claims.
PremisecitationInhaled air reaches 90% of the required temperature and humidity levels before reaching the nasopharynx, implicating the nasal cavity as the major conditioning apparatus in the respiratory tract.
“In fact, inhaled air reaches 90% of the required temperature and humidity levels before even reaching the nasopharynx, implicating the nasal cavity as the major conditioning apparatus in the respiratory tract [4,5].”
Quote in the paperSubstantial claim0 of 2 sources checkedMay combine two claims.
Interpretationnone givenMost previous studies of Qst-based craniofacial divergence employed anticonservative heritability assumptions that overestimate genetic differentiation and can lead to incorrect conclusions about selection versus drift.
“While this might be true, most of these studies employed anticonservative heritability assumptions, which overestimate the genetic differentiation underlying a trait, and thus, lead to incorrect conclusions regarding the relative roles of selection and drift in driving phenotypic differences among populations.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationWhen Qst is much greater than Fst, trait divergence exceeds neutral expectations and can be attributed to divergent selection.
“Thus, when Qst is much greater than Fst, trait divergence exceeds neutral expectations and can be attributed to divergent selection [11].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [11] MC Whitlock, 2009, Testing for spatially divergent selection: comparing QST to FST, Genetics source
Not checked in the free run.
May combine two claims.
PremisecitationThe efficacy of the conditioning process depends on the flow dynamics of the inspired air, which depend on the geometry of the nasal cavity and inlets.
“Studies have shown that the efficacy of the conditioning process depends on the flow dynamics of the inspired air, which in turn, depend on the geometry of the nasal cavity and inlets [5,7].”
Quote in the paperSubstantial claim0 of 2 sources checkedClassified as probably not a substantial claim.
PremisecitationDivergence in the shape of the external nose, at least between Europeans and Han Chinese populations, exceeds neutral expectations.
“More recently, it was also reported that the divergence in the shape of the external nose, at least between Europeans and Han Chinese populations, also exceeds neutral expectations [14].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [14] J Guo, 2014, Variation and signatures of selection on the human face, J Hum Evol source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationSkin pigmentation is known to have evolved in response to a geospatially varying selection pressure: exposure to ground level ultraviolet B radiation (UVB).
“Skin pigmentation is also a good example of a phenotype which is known to have evolved in response to a geospatially varying selection pressure: exposure to ground level ultraviolet B radiation (UVB) [23].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [23] NG Jablonski, 2000, The evolution of human skin coloration, J Hum Evol source
Not checked in the free run.
May combine two claims.
PremisecitationLow humidity in the respiratory tract leads to impaired mucociliary function and increases the risk of both upper and lower respiratory tract infections.
“Low humidity in the respiratory tract leads to impaired mucociliary function and increases the risk of both upper and lower respiratory tract infections [6].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [6] SH Randell, 2006, Effective mucus clearance is essential for respiratory health, Am J Respir Cell Mol Biol source
Not checked in the free run.
Classified as probably not a substantial claim.
Interpretationown dataThe conclusion that additive genetic variance between populations might be less than within populations is limited because heritabilities were estimated in individuals with W. African and European ancestry only and do not reflect variation within and across other populations.
“However, we are cautious of over-stating this conclusion since the heritabilities were estimated in individuals with W. African and European ancestry only and do not reflect the variation within and across other populations.”
Quote in the paperSubstantial claimMay combine two claims.
InterpretationreasoningIf the true value of c/h2 is drastically lower than 1, phenotype-derived estimates of the among-population genetic variance and Qst will be inflated, resulting in false-positive conclusions regarding the role of selection in driving phenotypic differentiation.
“If the true value of c/h2 is drastically lower than 1, phenotype-derived estimates of the among-population genetic variance, and hence, Qst will be inflated, resulting in false-positive conclusions regarding the role of selection in driving phenotypic differentiation.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S2 (checkable). May combine two claims.
InterpretationreasoningThe opposite case (c/h2 < 1) is more plausible because environmental variation is expected to be large across geographically distant populations.
“If anything, the opposite case (c/h2 < 1) is more plausible as we expect environmental variation to be large across geographically distant populations.”
Quote in the paperNot a substantial claim- Rests on an assumption: Environmental variation is large across geographically distant populations.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationHeight seems to be under positive selection within European and African populations separately.
“While height seems to be under positive selection within European and African populations separately [19,34], it does not appear to be driven by divergent selection pressures across the populations considered here.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [19] MC Turchin, 2012, Evidence of widespread selection on standing variation in Europe at height-associated SNPs, Nat Genet source
Not checked in the free run.
- cites [34] GH Perry, 2014, Adaptive, convergent origins of the pygmy phenotype in African rainforest hunter-gatherers, Proc Natl Acad Sci U S A source
Not checked in the free run.
Classified as probably not a substantial claim.
InterpretationreasoningAssuming c/h2 > 1 is an anticonservative approach because it assumes that heritability across populations is higher than heritability within populations.
“While this might be true for some traits (for example, see skin pigmentation in Table 3), this is an anticonservative approach in our opinion, because it assumes that the heritability across populations is higher than the heritability within populations.”
Quote in the paperSubstantial claimClassified as probably not a substantial claim.
Interpretationown dataThe effect of Northern European removal might be indicative of positive selection for lighter skin pigmentation and narrower nares in higher latitude populations.
“This effect might be indicative of positive selection for lighter skin pigmentation and narrower nares in higher latitude populations.”
Quote in the paperSubstantial claim- Rests on an assumption: The climate at the parents' birthplaces is a good proxy for the individual's ancestral climate.
May combine two claims.
Interpretationown dataBoth phenotype-climate correlations (skin pigmentation vs UVB and nares width vs temperature) are driven primarily by the inclusion of Northern Europeans.
“suggesting that both phenotype-climate correlations are driven primarily by the inclusion of N. Europeans.”
Quote in the paperSubstantial claim- Rests on an assumption: The climate at the parents' birthplaces is a good proxy for the individual's ancestral climate.
May combine two claims.
PremisecitationIn a randomly mating admixed population, ancestry segments segregate randomly with respect to the environment, which decouples the between-population genetic effects on the phenotype from the environmental effects, allowing for the estimation of the genetic variance underlying a phenotype.
“In a randomly mating admixed population, ancestry segments segregate randomly with respect to the environment, which decouples the between-population genetic effects on the phenotype from the environmental effects, allowing for the estimation of the genetic variance underlying a phenotype.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [39] A Darvasi, 2005, The beauty of admixture, Nat Genet source
Not checked in the free run.
Classified as probably not a substantial claim.
PremisecitationPrior studies have shown that nasal aperture and nasal cavity shapes are correlated with temperature and humidity, with individuals from cold-dry climates having narrower nasal cavities than individuals from warm-humid climates.
“Previously, several studies have shown that the shapes of the nasal aperture and nasal cavity are correlated with climate variables related to temperature and humidity such that individuals from cold-dry climates exhibit narrower nasal cavities compared to individuals from warm-humid climates [41,42].”
Quote in the paperSubstantial claim0 of 2 sources checkedClassified as probably not a substantial claim.
PremisecitationDifferences in skin pigmentation across human populations have evolved primarily in response to ultraviolet radiation.
“multiple lines of evidence suggest that differences in skin pigmentation across populations have evolved primarily in response to ultraviolet radiation [17,20–22].”
- Also stated in: § Discussion · boosted
“Substantial evidence has accumulated supporting the hypothesis that differences in skin pigmentation across human populations have evolved largely in response to selection pressures imposed by exposure to ultraviolet radiation [20].”
Quote in the paperSubstantial claim0 of 4 sources checked- cites [17] S Beleza, 2013, Genetic architecture of skin and eye color in an African-European admixed population. Spritz RA, editor, PLoS Genet source
Not checked in the free run.
- cites [20] NG Jablonski, 2004, the Evolution of Human Skin and Skin Color, Annu Rev Anthropol source
Not checked in the free run.
- cites [21] RL Lamason, 2005, SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans, Science source
Not checked in the free run.
- cites [22] HL Norton, 2007, Genetic evidence for the convergent evolution of light skin in Europeans and East Asians, Mol Biol Evol source
Not checked in the free run.
- Also stated in: § Discussion · boosted
Classified as probably not a substantial claim.
Study design and conductcitationThe top four genetic PCs were included as covariates in the model to correct for population structure, which can inflate heritability estimates.
“The top four genetic PCs were included as covariates in the model to correct for population structure, which can inflate heritability estimates [18,69,70].”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [18] J Yang, 2010, Common SNPs explain a large proportion of the heritability for human height, Nat Genet source
Not checked in the free run.
- cites [69] SR Browning, 2011, Population structure can inflate SNP-based heritability estimates, Am J Hum Genet source
Not checked in the free run.
- cites [70] ME Goddard, 2011, Response to browning and browning, Am J Hum Genet source
Not checked in the free run.
Classified as probably not a substantial claim.
Study design and conductown dataNon-independence among observations due to genetic similarity was taken into account by allowing the observations to be correlated according to the SNP-based genome-wide kinship matrix.
“We took non-independence among observations due to genetic similarity into account by allowing the observations to be correlated according to the SNP-based genome-wide kinship matrix.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationEcological selection and sexual selection could reinforce each other, accelerating phenotypic divergence across populations in spite of continued gene flow.
“Indeed, ecological selection and sexual selection could reinforce each other, accelerating phenotypic divergence across populations in spite of continued gene flow [54].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [54] GS van Doorn, 2009, On the origin of species by natural and sexual selection, Science source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationThe seven landmarks used for linear distances have been defined previously.
“These landmarks have been defined previously [1,26] and their approximate positions are shown in Fig 1.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [1] LG Farkas, 1986, Geography of the nose: a morphometric study, Aesthetic Plast Surg source
Not checked in the free run.
- cites [26] VF Ferrario, 2007, Three-dimensional computerized anthropometry of the nose: Landmark representation compared to surface analysis, Cleft Palate-Craniofacial J source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataSex, age, and BMI were also included as covariates in the c estimation.
“Sex, age, and BMI were also included as covariates.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataQuality-control steps sufficiently remove potential batch effects due to genotyping platform, as evidenced by a multidimensional scaling plot clustering individuals by ancestry and not by platform.
“This sufficiently removes any potential batch effects due to platform as evidenced by the observation that in a multidimensional scaling plot, individuals cluster by ancestry and not by platform (S1 Fig).”
Quote in the paperSubstantial claimClassified as probably not a substantial claim. May combine two claims.
Study design and conductcitationA spatially dense mesh of 7,150 quasi-landmarks was mapped onto each image and its reflection, resulting in homologous vertices and triangles across individuals.
“A spatially dense mesh of 7,150 quasi-landmarks (QLs) was mapped onto each image and its reflection. As a result of this mapping, the vertices and triangles are homologous across individuals [80].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [80] P Claes, 2015, An investigation of matching symmetry in the human pinnae with possible implications for 3D ear recognition and sound localization, J Anat source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataData collection was carried out with informed consent of participants and with approval from institutional review boards.
“Data collection was carried out with informed consent of participants and with approval from the institutional review boards (IRBs) at The Pennsylvania State University (IRB# 32341, IRB# 45727, IRB# 44929) and at The University of Illinois Urbana-Champaign (IRB# 13103).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisereasoningSexual selection has likely played an important role in human evolution, as evidenced by sexual dimorphism in many physical traits.
“Sexual selection has likely played an important role in human evolution, as evidenced by the presence of sexual dimorphism in many physical traits (e.g., height, waist-hip ratio, facial hair, and breasts to name a few).”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Study design and conductown dataA linear mixed model was used to test the relationship between phenotype and climate variables, while correcting for age and BMI.
“We used a linear mixed model to test the relationship between phenotype and climate variables, while correcting for age and BMI.”
Quote in the paperSubstantial claimMay combine two claims.
PremisecitationInhaled air reaches 90% of the required temperature and humidity levels before reaching the nasopharynx, implicating the nasal cavity, especially the turbinates, as the major conditioning apparatus in the respiratory tract.
“Inhaled air reaches 90% of the required temperature and humidity levels before even reaching the nasopharynx, implicating the nasal cavity, especially the turbinates, as the major conditioning apparatus in the respiratory tract [4,5].”
Quote in the paperSubstantial claim0 of 2 sources checkedClassified as probably not a substantial claim.
Study design and conductnone givenSensitivity curves were used to evaluate the behavior of Qst to cases where c < h2.
“However, we used sensitivity curves to evaluate the behavior of Qst to cases where c < h2.”
Quote in the paperSubstantial claim- The authors state this as an assumption: Within-population heritability equals among-population heritability (c = h2) when calculating Qst from phenotype data.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataSex, age, and BMI were included as covariates in the model for hg2 estimation.
“Also included in the model were sex, age, and BMI.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Study design and conductnone givenProcrustes coordinates of original and reflected images were averaged to remove effects of bilateral asymmetry.
“The Procrustes coordinates of the original and reflected image for each participant were then averaged to remove effects of bilateral asymmetry.”
Quote in the paperSubstantial claimClassified as probably not a substantial claim.
Study design and conductcitationGlobal ancestry was included as a covariate to correct for ancestry stratification and any environmental variables that might covary with ancestry.
“Global ancestry, calculated from the mean of local ancestry across all SNPs, was included as a covariate to correct for ancestry stratification and any environmental variables that might covary with ancestry [16,72].”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [16] EJ Parra, 2004, Implications of correlations between skin color and genetic ancestry for biomedical research, Nat Genet source
Not checked in the free run.
- cites [72] I Halder, 2003, Measuring and using admixture to study the genetics of complex diseases, Hum Genomics source
Not checked in the free run.
May combine two claims.
Study design and conductown dataThe use of inverse melanin index does not affect conclusions; untransformed melanin index produces similar results.
“Statistical testing was performed using the inverse of melanin index since it is more normally distributed (S7 Fig) but the use of untransformed melanin index produces similar results and does not affect our conclusions.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Study design and conductcitationGeneralized Procrustes Superimposition was carried out on original and reflected images to remove differences in position and orientation.
“Generalized Procrustes Superimposition [24] was carried out on both sets of images (original and reflected) to remove differences in position and orientation.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [24] JC Gower, 1975, Generalized procrustes analysis, Psychometrika source
Not checked in the free run.
Classified as probably not a substantial claim.
Study design and conductown dataThe association between phenotypes and climate variables was tested using linear mixed models that correct for age, BMI, and genetic similarity.
“The association between phenotypes and climate variables was tested using linear mixed models, which correct for age, BMI, and genetic similarity (Methods).”
Quote in the paperSubstantial claim
The authors state this as an assumption.
The ratio c/h2 is equal to 1, i.e., the proportion of phenotypic variance due to additive genetic effects is the same among- and within-populations.
“We estimated Qst under the assumption that c/h2 = 1. In other words, we assume that the proportion of between-population variance in the trait due to additive genetic effects is the same as the proportion of within-population variance due to additive genetic effects.”
The paper relies on this without support.
Most genetic variation in humans exists within populations.
“which agrees with the fact that most of the genetic variation in humans exists within populations.”
The paper relies on this without support.
Environmental variation is large across geographically distant populations.
“as we expect environmental variation to be large across geographically distant populations.”
The paper relies on this without support.
The nose functions to warm and humidify inspired air.
“The choice of these climate variables follows from the functional importance of the nose in warming and humidifying inspired air.”
The paper relies on this without support.
The climate at the parents' birthplaces is a good proxy for the individual's ancestral climate.
“This was done to assign to each individual, a climate value that was most similar to their ‘ancestral’ climate.”
The authors state this as an assumption.
Within-population heritability equals among-population heritability (c = h2) when calculating Qst from phenotype data.
“studies often calculate Qst directly from phenotype data under the assumption that the within-population heritability (h2) is equal to the among-population heritability (c).”
“Our approach is similar to previous studies in that we also estimated Qst assuming c = h2.”
The paper relies on this without support.
Genetic variation between populations is less than genetic variation within populations for most phenotypes.
“In fact, genetic variation between-populations is likely to be less than the genetic variation within-populations for most phenotypes.”
The paper relies on this without support.
High values of Qst–Fst are indicative of divergent selection.
“High values of Qst–Fst are indicative of divergent selection, and the empirical p-value for this test was determined by calculating the proportion of Qst–Fst values that are less than zero.”
The paper relies on this without support.
The climate at the parents' birthplace represents the ancestral climate for each individual.
“We used climate values at the parents’ birthplace to represent the ancestral climate for each individual.”
The paper relies on this without support.
The Fst distribution from the 118,420 SNPs represents neutral genetic divergence.
“Values of Fst were simulated by randomly sampling from the Fst of 118,420 SNPs (S3 Fig).”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The variation due to local ancestry that local-ancestry-based heritability estimation leverages has no clear relationship with between-group trait differences.
“We show that the variation due to local ancestry that they leverage has no clear relationship with between-group trait differences.”
From Heritability within groups is uninformative about differences among groups: Cases from behavioral, evolutionary, and statistical genetics (2024) · cites this paper as [16]
The Results section (“Investigating heritability of nose shape within- and among-populations”; page unavailable) says local-ancestry variation represents genetic variation between populations. It explicitly treats the phenotypic variance explained by local ancestry as conceptually equivalent to the genetic contribution to between-population phenotypic variation, rather than having no clear relationship to it. (LLM, conf=0.87)
Checked by a reasoning model — may be wrong.
Experimental — accuracy not yet measuredSkin pigmentation is strongly associated with absolute latitude; populations further from the equator have lighter skin pigmentation.
“As previously observed (Byard, 1981; Jablonski and Chaplin, 2010; Zaidi et al., 2017), we find that skin pigmentation is strongly associated with absolute latitude (R2=0.53, β=−1.18 on M index scale, p<2e-16); populations further from the equator have lighter skin pigmentation.”
From An Unexpectedly Complex Architecture for Skin Pigmentation in Africans (2017) · cites this paper as Zaidi et al., 2017
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Table 1 labels area measurements in millimeters rather than square millimeters
MinorTable 1 gives both area columns units of mm, but the methods specify mm2 for these measurements.
“| External surface area (mm) | Nostril area (mm) |”
“We also computed two areas (measured in mm2): i. total external area of the nose and ii. mean nostril area (Fig 1) (Methods).”
Cites
PLINK: a tool set for whole-genome association and population-based linkage analyses.
Purcell, S., Neale, B., Todd-Brown, K., Thomas, L., Ferreira, M. A. R., Bender, D., Maller, J., Sklar, P., de Bakker, P. I. W., Daly, M. J., et al. (2007) · The American Journal of Human Genetics · doi:10.1086/519795 · Cited by 34,089 · see citing works
ESTIMATING F -STATISTICS FOR THE ANALYSIS OF POPULATION STRUCTURE
Weir, B. S., & Cockerham, C. C. (1984) · Evolution · doi:10.1111/j.1558-5646.1984.tb05657.x · Cited by 18,909 · see citing works
Second-generation PLINK: rising to the challenge of larger and richer datasets
Chang, C. C., Chow, C. C., Tellier, L. C., Vattikuti, S., Purcell, S. M., & Lee, J. J. (2015) · Gigascience · doi:10.1186/s13742-015-0047-8 · Cited by 12,709 · see citing works
Estimating F-Statistics for the Analysis of Population Structure
Weir, B. S., & Cockerham, C. C. (1984) · Evolution · doi:10.2307/2408641 · Cited by 11,023 · see citing works
nlme : Linear and nonlinear mixed effects models
DebRoy, S. (2006) · Medical Entomology and Zoology · Cited by 10,009 · see citing works
GCTA: a tool for genome-wide complex trait analysis
Yang, J., Lee, S. H., Goddard, M. E., & Visscher, P. M. (2011) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2010.11.011 · Cited by 8,279 · see citing works
nlme: Linear and Nonlinear Mixed Effects Models
Pinheiro, J., R Core Team, & Bates, D. (1999) · doi:10.32614/cran.package.nlme · Cited by 6,867 · see citing works
THE GENETICAL STRUCTURE OF POPULATIONS
Wright, S. (1949) · Annals of Eugenics · doi:10.1111/j.1469-1809.1949.tb02451.x · Cited by 6,729 · see citing works
Genetics and Analysis of Quantitative Traits
(2002) · Journal of Animal Breeding and Genetics · doi:10.1046/j.1439-0388.2002.00356.x · Cited by 6,172 · see citing works
Updated high‐resolution grids of monthly climatic observations – the CRU TS3 .10 Dataset
Harris, I. C., Jones, P. D., Osborn, T. J., & Lister, D. (2013) · International Journal of Climatology · doi:10.1002/joc.3711 · Cited by 6,121 · see citing works
Common SNPs explain a large proportion of the heritability for human height
Yang, J., Benyamin, B., McEvoy, B. P., Gordon, S., Henders, A. K., Nyholt, D. R., Madden, P. A., Heath, A. C., Martin, N. G., Montgomery, G. W., et al. (2010) · Nature Genetics · doi:10.1038/ng.608 · Cited by 4,446 · see citing works
Generalized procrustes analysis
Gower, J. C. (1975) · Psychometrika · doi:10.1007/bf02291478 · Cited by 3,267 · see citing works
Genome-wide detection and characterization of positive selection in human populations
The International HapMap Consortium, Sabeti, P. C., Varilly, P., Fry, B., Lohmueller, J., Hostetter, E., Cotsapas, C., Xie, X., Byrne, E. H., McCarroll, S. A., et al. (2007) · Nature · doi:10.1038/nature06250 · Cited by 2,131 · see citing works
ggmap: Spatial Visualization with ggplot2
Kahle, D. J., & Wickham, H. (2013) · The R Journal · doi:10.32614/rj-2013-014 · Cited by 2,126 · see citing works
The evolution of human skin coloration
Jablonski, N. G., & Chaplin, G. (2000) · Journal of Human Evolution · doi:10.1006/jhev.2000.0403 · Cited by 1,212 · see citing works
SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans
Lamason, R. L., Mohideen, M.-A. P. K., Mest, J. R., Wong, A. C., Norton, H. L., Aros, M. C., Jurynec, M. J., Mao, X., Humphreville, V. R., Humbert, J. E., et al. (2005) · Science · doi:10.1126/science.1116238 · Cited by 1,043 · see citing works
Self-citationBeauty and the beast: mechanisms of sexual selection in humans
Puts, D. A. (2010) · Evolution and Human Behavior · doi:10.1016/j.evolhumbehav.2010.02.005 · Cited by 824 · see citing works
Population structure in Daphnia obtusa: quantitative genetic and allozymic variation.
Spitze, K. (1993) · Genetics · doi:10.1093/genetics/135.2.367 · Cited by 797 · see citing works
Skin pigmentation, biogeographical ancestry and admixture mapping
Shriver, M. D., Parra, E. J., Dios, S., Bonilla, C., Norton, H., Jovel, C., Pfaff, C., Jones, C., Massac, A., Cameron, N., et al. (2003) · Human Genetics · doi:10.1007/s00439-002-0896-y · Cited by 549 · see citing works
Self-citationQST–FST comparisons: evolutionary and ecological insights from genomic heterogeneity
Leinonen, T., McCairns, R. J. S., O'Hara, R. B., & Merilä, J. (2013) · Nature Reviews Genetics · doi:10.1038/nrg3395 · Cited by 422 · see citing works
Craniometric variation among modern human populations
Relethford, J. H. (1994) · American Journal of Physical Anthropology · doi:10.1002/ajpa.1330950105 · Cited by 418 · see citing works
Genetic evidence for the convergent evolution of light skin in Europeans and East Asians
Norton, H. L., Kittles, R. A., Parra, E., McKeigue, P., Mao, X., Cheng, K., Canfield, V. A., Bradley, D. G., McEvoy, B., & Shriver, M. D. (2006) · Molecular Biology and Evolution · doi:10.1093/molbev/msl203 · Cited by 410 · see citing works
Self-citationTesting environmental and genetic effects in the presence of spatial autocorrelation
Rousset, F., & Ferdy, J. (2014) · Ecography · doi:10.1111/ecog.00566 · Cited by 397 · see citing works
Evolutionary inference from <i>Q</i> <sub>ST</sub>
WHITLOCK, M. C. (2008) · Molecular Ecology · doi:10.1111/j.1365-294x.2008.03712.x · Cited by 384 · see citing works
The evolution of human skin and skin color
Jablonski, N. G. (2004) · Annual Review of Anthropology · doi:10.1146/annurev.anthro.33.070203.143955 · Cited by 367 · see citing works
Roseman, C. C. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0402637101 · Cited by 356 · see citing works
On the origin of species by natural and sexual selection
van Doorn, G. S., Edelaar, P., & Weissing, F. J. (2009) · Science · doi:10.1126/science.1181661 · Cited by 342 · see citing works
Effective mucus clearance is essential for respiratory health
Randell, S. H., & Boucher, R. C. (2006) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2006-0082sf · Cited by 335 · see citing works
Evidence of widespread selection on standing variation in Europe at height-associated SNPs
Turchin, M. C., Chiang, C. W., Palmer, C. D., Sankararaman, S., Reich, D., Genetic Investigation of ANthropometric Traits (GIANT) Consortium, & Hirschhorn, J. N. (2012) · Nature Genetics · doi:10.1038/ng.2368 · Cited by 329 · see citing works
A Genome-Wide Association Study Identifies Five Loci Influencing Facial Morphology in Europeans
Liu, F., van der Lijn, F., Schurmann, C., Zhu, G., Chakravarty, M. M., Hysi, P. G., Wollstein, A., Lao, O., de Bruijne, M., Ikram, M. A., et al. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002932 · Cited by 326 · see citing works
Lande, R. (1992) · Evolution · doi:10.1111/j.1558-5646.1992.tb02046.x · Cited by 274 · see citing works
Climate-related variation of the human nasal cavity
Noback, M. L., Harvati, K., & Spoor, F. (2011) · American Journal of Physical Anthropology · doi:10.1002/ajpa.21523 · Cited by 272 · see citing works
Modeling 3D Facial Shape from DNA
Claes, P. D., Liberton, D. K., Daniels, K., Rosana, K. M., Quillen, E. E., Pearson, L. N., McEvoy, B., Bauchet, M., Zaidi, A. A., Yao, W., et al. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004224 · Cited by 247 · see citing works
Self-citationGeography of the nose: a morphometric study
Farkas, L. G., Kolar, J. C., & Munro, I. R. (1986) · Aesthetic Plastic Surgery · doi:10.1007/bf01575292 · Cited by 245 · see citing works
Fast and accurate inference of local ancestry in Latino populations
Baran, Y., Paşaniuc, B., Sankararaman, S., Torgerson, D. G., Gignoux, C. R., Eng, C. S., Rodríguez-Cintrón, W., Chapela, R., Ford, J. G., Avila, P. C., et al. (2012) · Bioinformatics · doi:10.1093/bioinformatics/bts144 · Cited by 243 · see citing works
Leinonen, T., Cano, J. M., Mäkinen, H., & Merilä, J. (2006) · Journal of Evolutionary Biology · doi:10.1111/j.1420-9101.2006.01182.x · Cited by 240 · see citing works
Multivariate apportionment of global human craniometric diversity
Roseman, C. C., & Weaver, T. D. (2004) · American Journal of Physical Anthropology · doi:10.1002/ajpa.10424 · Cited by 236 · see citing works
Implications of correlations between skin color and genetic ancestry for biomedical research
Parra, E. J., Kittles, R. A., & Shriver, M. D. (2004) · Nature Genetics · doi:10.1038/ng1440 · Cited by 220 · see citing works
Self-citationIdentifying positive selection candidate loci for high-altitude adaptation in Andean populations
Bigham, A. W., Mao, X., Mei, R., Brutsaert, T. D., Wilson, M. J., Julian, C. G., Parra, E. J., Akey, J. M., MOORE, L. G., & Shriver, M. D. (2009) · Human Genomics · doi:10.1186/1479-7364-4-2-79 · Cited by 219 · see citing works
Self-citationClimate signatures in the morphological differentiation of worldwide modern human populations
Hubbe, M., Hanihara, T., & Harvati, K. (2009) · The Anatomical Record · doi:10.1002/ar.20976 · Cited by 217 · see citing works
Variation in human nasal height and breadth
Franciscus, R. G., & Long, J. C. (1991) · American Journal of Physical Anthropology · doi:10.1002/ajpa.1330850406 · Cited by 215 · see citing works
Paternoster, L., Zhurov, A. I., Toma, A. M., Kemp, J. P., Pourcain, B. S., Timpson, N. J., McMahon, G., McArdle, W. L., Ring, S. M., Smith, G. D., et al. (2012) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2011.12.021 · Cited by 215 · see citing works
Adhikari, K., Fuentes-Guajardo, M., Quinto-Sánchez, M., Mendoza-Revilla, J., Camilo Chacón-Duque, J., Acuña-Alonzo, V., Jaramillo, C., Arias, W., Lozano, R. B., Pérez, G. M., et al. (2016) · Nature Communications · doi:10.1038/ncomms11616 · Cited by 200 · see citing works
Storz, J. F. (2002) · Molecular Ecology · doi:10.1046/j.1365-294x.2002.01636.x · Cited by 195 · see citing works
Whither Pst? The approximation of Qst by Pst in evolutionary and conservation biology
BROMMER, J. E. (2011) · Journal of Evolutionary Biology · doi:10.1111/j.1420-9101.2011.02268.x · Cited by 194 · see citing works
The Air-Conditioning Capacity of the Human Nose
Naftali, S., Rosenfeld, M., Wolf, M., & Elad, D. (2005) · Annals of Biomedical Engineering · doi:10.1007/s10439-005-2513-4 · Cited by 193 · see citing works
Testing for Spatially Divergent Selection: Comparing <i>Q</i>ST to <i>F</i>ST
Whitlock, M. C., & Guillaume, F. (2009) · Genetics · doi:10.1534/genetics.108.099812 · Cited by 180 · see citing works
Morphological variation and airflow dynamics in the human nose
Churchill, S. E., Shackelford, L. L., Georgi, J. N., & Black, M. T. (2004) · American Journal of Human Biology · doi:10.1002/ajhb.20074 · Cited by 174 · see citing works
Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology
Shaffer, J. R., Orlova, E., Lee, M. K., Leslie, E. J., Raffensperger, Z. D., Heike, C. L., Cunningham, M. L., Hecht, J. T., Kau, C. H., Nidey, N., et al. (2016) · PLoS Genetics · doi:10.1371/journal.pgen.1006149 · Cited by 168 · see citing works
Genetic Architecture of Skin and Eye Color in an African-European Admixed Population
Beleza, S., Johnson, N. A., Candille, S. I., Absher, D. M., Coram, M. A., Lopes, J., Campos, J., Araújo, I. I., Anderson, T. M., Vilhjálmsson, B. J., et al. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003372 · Cited by 161 · see citing works
Self-citationAdaptive heterothermy and selective brain cooling in arid-zone mammals
Mitchell, D., Maloney, S. K., Jessen, C., et al. (2002) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/s1096-4959(02)00012-x · Cited by 150 · see citing works
Selective brain cooling in humans: “fancy” or fact?
Cabanac, M. (1993) · The FASEB Journal · doi:10.1096/fasebj.7.12.8375612 · Cited by 140 · see citing works
Lande, R. (1992) · Evolution · doi:10.2307/2409859 · Cited by 113 · see citing works
Candille, S. I., Absher, D. M., Beleza, S., Bauchet, M., McEvoy, B., Garrison, N. A., Li, J. Z., Myers, R. M., Barsh, G. S., Tang, H., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0048294 · Cited by 111 · see citing works
Self-citationEcogeographic variation in human nasal passages
Yokley, T. R. (2009) · American Journal of Physical Anthropology · doi:10.1002/ajpa.20893 · Cited by 105 · see citing works
Adaptive, convergent origins of the pygmy phenotype in African rainforest hunter-gatherers
Perry, G. H., Foll, M., Grenier, J.-C., Patin, E., Nédélec, Y., Pacis, A., Barakatt, M., Gravel, S., Zhou, X., Nsobya, S. L., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1402875111 · Cited by 105 · see citing works
Handbook of anthropometry : physical measures of human form in health and disease
Preedy, V. R. (2012) · Digital Access to Libraries (Université catholique de Louvain (UCL), l'Université de Namur (UNamur) and the Université Saint-Louis (USL-B)) · doi:10.1007/978-1-4419-1788-1 · Cited by 101 · see citing works
Weiner, J. S. (1954) · American Journal of Physical Anthropology · doi:10.1002/ajpa.1330120412 · Cited by 98 · see citing works
Population structure can inflate SNP-based heritability estimates
Browning, S. R., & Browning, B. L. (2011) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2011.05.025 · Cited by 96 · see citing works
Measuring and using admixture to study the genetics of complex diseases
Halder, I., & Shriver, M. D. (2003) · Human Genomics · doi:10.1186/1479-7364-1-1-52 · Cited by 93 · see citing works
Self-citationDarvasi, A., & Shifman, S. (2005) · Nature Genetics · doi:10.1038/ng0205-118 · Cited by 84 · see citing works
A Theoretical Model of Localized Heat and Water Vapor Transport in the Human Respiratory Tract
Hanna, L. M., & Scherer, P. W. (1986) · Journal of Biomechanical Engineering · doi:10.1115/1.3138574 · Cited by 82 · see citing works
Irmak, M. K., Korkmaz, A., & Eroğul, O. (2004) · Medical Hypotheses · doi:10.1016/j.mehy.2004.05.003 · Cited by 67 · see citing works
Leveraging population admixture to characterize the heritability of complex traits
Zaitlen, N., Pasaniuc, B., Sankararaman, S., Bhatia, G., Zhang, J., Gusev, A., Young, T., Tandon, A., Pollack, S., Vilhjálmsson, B. J., et al. (2014) · Nature Genetics · doi:10.1038/ng.3139 · Cited by 63 · see citing works
Variation and signatures of selection on the human face
Guo, J., Tan, J., Yang, Y., Zhou, H., Hu, S., Hashan, A., Bahaxar, N., Xu, S., Weaver, T. D., Jin, L., et al. (2014) · Journal of Human Evolution · doi:10.1016/j.jhevol.2014.08.001 · Cited by 54 · see citing works
Maddux, S. D., Yokley, T. R., Svoma, B. M., & Franciscus, R. G. (2016) · American Journal of Physical Anthropology · doi:10.1002/ajpa.23032 · Cited by 41 · see citing works
Wu, T., Li, S., & Ward, M. P. (2005) · Wilderness and Environmental Medicine · doi:10.1580/pr04-04.1 · Cited by 36 · see citing works
Beleza, S., Campos, J., Lopes, J., Araujo, I. I., Almada, A. H., Silva, A. C. E., Parra, E., & Rocha, J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0051103 · Cited by 34 · see citing works
Claes, P., Reijniers, J., Shriver, M. D., Snyders, J., Suetens, P., Nielandt, J., De Tré, G., & Vandermeulen, D. (2015) · Journal of Anatomy · doi:10.1111/joa.12252 · Cited by 32 · see citing works
Self-citationRegulation of brain temperature in winter-acclimatized reindeer under heat stress
Blix, A. S., Walløe, L., & Folkow, L. P. (2011) · Journal of Experimental Biology · doi:10.1242/jeb.057455 · Cited by 30 · see citing works
Hetem, R. S., Strauss, W. M., Fick, L. G., et al. (2012) · Journal of Experimental Biology · doi:10.1242/jeb.074666 · Cited by 24 · see citing works
Maloney, S. K., Mitchell, D., & Blache, D. (2006) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00275.2006 · Cited by 22 · see citing works
Introduction to the comparative anatomy of the nose and paranasal sinuses.
NEGUS, V. E. (1954) · PubMed · Cited by 20 · see citing works
RNetCDF - A Package for Reading and Writing NetCDF Datasets
Michna, P., & Woods, M. (2013) · The R Journal · doi:10.32614/rj-2013-023 · Cited by 19 · see citing works
CFD Simulations on the Heating Capability in a Human Nasal Cavity
Inthavong, K., Tian, Z. F., & Tu, J. (2007) · Cited by 18 · see citing works
He, Y., Li, R., Wang, J., Blanchet, S., & Lek, S. (2013) · ZOOLOGICAL SCIENCE · doi:10.2108/zsj.30.475 · Cited by 16 · see citing works
Response to browning and browning
Goddard, M. E., Lee, S. H., Yang, J., Wray, N. R., & Visscher, P. M. (2011) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2011.05.022 · Cited by 15 · see citing works
Numerical simulation and nasal air-conditioning
Keck, T., & Lindemann, J. (2011) · GMS current topics in otorhinolaryngology, head and neck surgery · doi:10.3205/cto000072 · Cited by 14 · see citing works
Ferrario, V. F., Mian, F., Peretta, R., Rosati, R., & Sforza, C. (2007) · The Cleft Palate-Craniofacial Journal · doi:10.1597/06-021 · Cited by 14 · see citing works
Crandall, C. G., Brothers, R. M., Zhang, R., et al. (2011) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01375.2010 · Cited by 14 · see citing works
RNetCDF – A Package for Reading and Writing NetCDF Datasets
Michna, P., & Woods, M. (2013) · Lincoln (University of Nebraska) · doi:10.7892/boris.47220 · Cited by 13 · see citing works
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Research works printed but not linked: 1
- A Nucara, 2012, Handbook of Anthropometry, Handb Anthr, 91
Cited by
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An Unexpectedly Complex Architecture for Skin Pigmentation in Africans
Martin, A. R., Lin, M., Granka, J. M., Myrick, J. W., Liu, X., Sockell, A., Atkinson, E. G., Werely, C. J., Möller, M., Sandhu, M. S., et al. (2017) · Cell · doi:10.1016/j.cell.2017.11.015 · Cited by 156 · see citing works
Schraiber, J. G., & Edge, M. D. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2319496121 · Cited by 17 · see citing works
- Authors
- Zaidi, A. A., Mattern, B. C., Claes, P., McEcoy, B., Hughes, C., & Shriver, M. D.
- Affiliations
- Pennsylvania State University (US)
- KU Leuven (BE)
- Trinity College Dublin (IE)
- University of Illinois Urbana-Champaign (US)
- Corresponding author
- Zaidi, Arslan A.
- Shriver, Mark D.
- Venue
- PLOS Genetics
- Publisher
- Public Library of Science (PLoS)
- Published
- 2017-03-16
- Volume
- 13
- Issue
- 3
- Pages
- e1006616
- ISSN
- 1553-7390 (ISSN-L)
- 1553-7404
- PMC
- PMC5354252
- OpenAlex
- W2596158197
- Semantic Scholar
- 0cb1254a036cffa43635d7a10c1fbd441ecc33df
- Cited by
- 117
- References
- 81
- Citations by year
- 2026: 12 · 2025: 11 · 2024: 8 · 2023: 15 · 2022: 12 · 2021: 19 · 2020: 15 · 2019: 11 · 2018: 13 · 2017: 1
- FWCI
- 15.16
- Type
- journal article
- Language
- en
- Update notices
- correction (2018-01-31)
- Open access
- gold
- doi.org
- Licence
- Locations
- PLoS Genetics (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Lirias (KU Leuven) (submittedVersion, other-oa)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Figshare (submittedVersion, cc-by)
- Funders
- U.S. Department of Defense
- University of Pennsylvania
- Pennsylvania State University
- Vlaamse regering
- University of Illinois at Urbana-Champaign
- Topics
- Physical Sciences › Mathematics › Geometry and Topology › Morphological variations and asymmetry
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic diversity and population structure
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Evolution and Genetic Dynamics
- Keywords
- climate change adaptation, local adaptation, nasal cavity, alar base width, genetic differentiation, air conditioning, absolute humidity, temperature, relative humidity, sexual selection, human evolution
- MeSH terms
- Adaptation, Physiological, Africa, Asia, Climate, Europe, Female, Genetics, Population, Geography, Humans, Humidity, Male, Nose, Selection, Genetic, Temperature, Genetic Drift, Black People, White People, Asian People
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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