Cogelites

Rienzi will love this one:
August 15, 2008 -- A gifted 15-year-old student from India had to be rushed to the hospital after drinking liquid nitrogen during a science class at Princeton University.

The class was part of a program run by the Connecticut-based Summer Institute for the Gifted.

(Via Bayblab.)

"Ethnic dislikes" of Americans ca. 1938

In screening for subjects for a reeducation experiment, Gregory Razran collected data on the "ethnic attitudes" of 150 Americans (about 100 college students from Columbia and Barnard and 50 middle-aged New Yorkers) in the 1930s, using 'a special "ethnic surnames plus nonethnic photographs" rating method' along with interviews of some subjects. Razran finds [1]:
The evidence for the existence of very definite unfavorable stereotypes and dislikes of Jews and Italians, and to a small extent also of Irish, is unmistakable. Photographs to which Jewish surnames had been attached dropped, as seen from Table 3, 1.21 points in General Liking, 0.81 in Character, 0.29 in Beauty, while going up 1.01 in Ambition and 0.36 in Intelligence, with little consistent change in Entertainingness. The photographs with Italian surnames went down 0.78 points in General Liking, 0.33 in Beauty, 0.35 in Intelligence, 0.45 in Character, 0.34 in Entertainingness, while going up 0.39 points in Ambition. The Irish surnames produced a drop of 0.25 points in General Liking, 0.12 points in Beauty, 0.19 in Intelligence, 0.29 in Character, o.i i points in Entertainingness and a rise of 0.18 points in Ambition. The drops in General Liking and Character for Jews and Italians and the rise in Ambition for Jews are fully reliable statistically, while the other drops and rises possess some degree of reliability, are consistent, and borne out, in the main, by the interviews. The results are even more striking if one considers the fact that nearly 30 per cent of the subjects showed no consistent changes in their ratings and were—as revealed by some post-ratings questionings — definitely free from ethnic dislike.
In contrast, "changes in the ratings of the photographs with Old American surnames" were "few and in no case statistically reliable".

Contrary to what one might expect based on the rantings of various German-identified types, the Anglo-Saxons in this sample are not overly philo-Semitic--just the opposite:
ethnic dislike and unfavorable stereotyping of Jews among Americans of different ethnic descents diminishes in the following order [n/a: line breaks added]:

Anglo-Saxon,
German,
Scandinavian,
Dutch,
Irish,
French,
Spanish,
Italian,
Slav,
Hungarian,
Baltic,
Greek,
Rumanian.

[. . .]

The dislikes and unfavorable stereotypings of Italians follow approximately the same order, except that here the differences do not become statistically reliable till we pit those of Anglo-Saxon, German, Scandinavian, Irish, and Dutch descents against those who descend from white ethnic groupings in Eastern and Southern Europe (including the Jews among the latter).

Regional differences seem minimal, but in this sample, at least, Mid-Atlantic and New England residents like Jews the least and Southerners like Jews the most.
Also of interest, dislike of Jews peaks among the middle-class and middle-income, while dislike of Italians continues to rise with income (on the whole, all occupation/income groups dislike both Jews and Italians; only the degree varies):
From Table 5 we learn that college students are less prejudiced against Jews when their parents' incomes are either less than $3,000 or more than $12,000 than when these incomes are in intermediate brackets; that the parents' college education lessens a little the prejudices of their children; and that children of professionals, laborers, and big businessmen have less Jewish prejudice than children of farmers, white-collar workers, and small businessmen. The differences in amount of Jewish prejudice between the children of professionals and white-collar workers are fully reliable statistically, while the other differences are fairly or somewhat reliable. On the other hand, this table shows that prejudice against Italians is smaller among children of white-collar workers and small businessmen than among children of laborers and big businessmen; and that this prejudice is little affected by the education of the parents of the students, and is the greater the higher the income of the parents.
Additionally:
prejudice against Jews is greater among Republicans than among Democrats, among opponents than among proponents of the New Deal (in 1938), among men students than among women students, among students who are members of sororities or fraternities than among those who are not members of these organizations, and among those who spent part of their lives in rural communities. Prejudice against Italians is, on the other hand, unrelated to political party preferences, attitudes toward the New Deal, and residence in rural communities. [. . .] Both prejudices are less among Catholics than among Protestants—very much less in the prejudice against Italians—but in this study religious affiliations have been so much overshadowed by ethnic descent that not much significance should be attached to this finding.
Razran concludes:
that among present-day Americans ethnic dislike and unfavorable stereotyping of Jews possess an extent, a quality, and a structure that mark them off significantly from the dislike and unfavorable stereotyping of a comparable group such as Italians, not to mention the mild dislike and unfavorable stereotyping of the Irish. Merely quantitatively, in terms of standard scores, the mean of ethnic dislike of Jews is about 50 per cent higher than that of Italians and about five times as great as the dislike of the Irish. [Freudian psychobabble excised.]

For one thing, in some areas that are no doubt determinants of ethnic—or any other social—status, the Jews have been judged favorably, or only slightly or moderately unfavorably. Take, for instance, intelligence and education—or rather a lack of them. The adjectives "ignorant," "stupid," "uncivilized," "primitive," "nai've," and the like have been applied very lavishly to the Italians in this study, and to some small extent also to the Irish. But in the case of the Jews the stereotyping was, as seen from the tables, in a favorable direction, with only occasional unfavorable Comments in the interviews such as "Jewish intelligence lacks originality," is "destructive," or is "too verbal and academic," and the like. In another area, that of "hygiene" and "grooming" and the adjectives of "dirty," "smelly," "sloppy," the stereotype of Jews was only a little more unfavorable than that of the Irish and clearly less unfavorable than that of the Italians.

[. . .]

In two other social realms that unquestionably are determining factors in ethnic status and distance, the Jews were judged moderately unfavorably. These realms are, first, what may be called "manners," "etiquette," and "taste," and, secondly, emotional stability. Neither of these realms has come in for direct rating, but both of them have been important in setting the rating of General Liking—to a considerable extent also Character and Entertainingness— and both have figured heavily in the interviews. In the first realm, the characterizations of "loud," "gaudy," "vulgar," "ostentatious," "uncouth," "don't know how to behave," often dubbed both Jews and Italians. There was, however, this difference that the ill-manners of the Italians were attributed to ignorance and to what may be called a "culture lag"—using culture in its popular rather than its sociological connotation—while Jewish bad manners were said to stem from more basic character defects which, as will be seen later, are the crux and "focal organizer" of nearly all the prejudice toward Jews. The unfavorable stereotyping with regard to emotional stability was "neuroticism" for the Jews, "irresponsibility," "hot air," and "alcoholism," for the Irish, and "hot tempered," "impulsive," "revengeful," and "primitive emotionality," for the Italians. Again, there was a tendency to consider the alleged instability of the Jews as socially more offensive, even though it was admitted that in concrete social situations the alleged instability of the other two groups would be more likely to be harmful and disruptive.

Except for General Liking, Jews scored lowest in Character and highest in Ambition. However, while Ambition is quite a specific aspect of behavior to be rated, Character is of course very composite, and we must turn to the interviews for specifications. On the whole, the chief determinants of the very low Jewish scores in Character was the stereotype of their unethical conduct—"unscrupulous," "dishonest," "crooked," "unfair," "scheming," "egotistic," "egocentric,"—with the stereotypes of "aggression," "cowardice," and "ill-manners" following in order.
Continuing, Razran finds:
Another distinguishing characteristic, this time a favorable one, of attitudes toward Jews is the considerable number of individuals whose attitudes and stereotyping clearly class them as pro-Jewish. (Excluding self-ratings no comparable pro-Italian and pro-Irish groups, to speak of, were found.) There were 29 such individuals—15 per cent— in this study, and 12 of them were interviewed. In three of the 12, the pro- Jewishness was primarily a matter of ethics, Christian ethics, a desire to help the downtrodden, to atone for the "sins of the fathers," and in at least one of the three, these feelings were tied up with an unhappy frustrated personal life. The pro-Jewishness of the remaining nine was, however, little governed by such considerations, but seemed to stem directly from a conviction that the Jews are a superior group in most, if not in all, personal and social qualities. Among the students, this alleged superiority revolved around Jewish contributions to civilization, their preeminent and forward ideas and ideals, almost a belief that most positive qualities of Western culture are largely due to Jews. In some ways, the views of these non-Jewish Americans correspond to the doctrine of a "Jewish mission:" "peace and love," as preached by some American rabbis; "revolution and a new social order," as put forth by some early Russian-Jewish revolutionaries. On the other hand, the pro-Jewish subjects of the middle-aged group saw Jewish superiority primarily in the personal success, achievements, and habits of the latter. Said a small storekeeper of Irish descent: "I take my hat off to the Jews. They know how to do things and get things, despite handicaps I certainly would be happy if my daughter married a Jew. Jews are good family people, good providers, loyal to their wife and children, and don't drink."

The general curve of the distribution of dislike-like of Jews also seems to differ from the curves of dislike-like of the two other ethnic groups, as may be gathered from Table 8. The curves for both Italians and Irish are essentially unimodal, the first being bell-shaped and the second being positively skewed, but the curve for the Jews unmistakably points toward a bi-modality of distribution.

[1] Razran, G. Ethnic dislikes and stereotypes: a laboratory study. The Journal of Abnormal and Social Psychology. Vol. 45(1), January 1950, pp. 7-27.

The "discrepancy" between the recent European genetic structure paper and earlier studies

There is none that I can see.

Lao et al. write:
Previous studies based on genome-wide SNP diversity reported differences between individuals of southern and northern/central European ancestry [3, 5, 6] and, to a lesser extent, between those of eastern and western European ancestry [3], which were not confirmed in our study.

However, looking at the earlier studies cited and comparing like to like, the picture is broadly similar: the main axis of genetic variation in Europe is North-South; Greeks and Italians are cleanly separable from Northern Europeans. The N-S gap is bridged somewhat by central Europeans and Iberians, but (unmixed) Iberians in particular are numerically insignificant in the U.S.

Regardless of whether genetic variation is "clinal" or "clustered" within Europe, America's Northern European majority is genetically distinct from its southern Italian minority.

The image at left shows Utah whites (the "CEU" HapMap population) overlaid on the PCA plot of European populations generated by Lao et al. Clearly, Utah whites are not going to be confused with Italians, "small" differences or not.

Other points:

As discussed elsewhere, the "UK" sample is a reference sample from London and likely contains many individuals with Irish, Welsh, and Scottish forebears. It should not be taken as representative of the English, or used as the basis for arguments about the genetic impact of historical migrations.

The People of the British Isles project should allow finer-scale comparisons within northwestern Europe.
To determine the genetic patterns across the British Isles, we will use genetic “markers” to look at every individual sample. One might expect, for example, to find fewer genetic differences between people in Cornwall and Devon than Cornwall and the Shetlands because, historically, there has been less movement between the more distant counties.

Once these genetic patterns have been identified, it should also be possible to use them to investigate historical patterns of movement within the UK. As well as this, comparison of these patterns with results from other populations that surround the UK, such as the Scandanavians, French and Germans, should help us to understand the impact they have had on the British over the Centuries.

[. . .]

What we plan to do is collect blood samples from between 100 and 150 people from about 30 different rural regions throughout the UK. To try and make sure that the sample is representative of the area throughout the ages, we are looking for people whose parents and grandparents were all born in the same locality.

The goal is 3500 samples, of which the project website reports 3294 have been collected. According to the May 2008 newsletter (pdf):
We are currently in the process of analysing our data from the latest round of genotyping and hope to report the results later on this year.

"Physical Characteristics of True Americans"

In the eyes of "2nd-generation Americans" [1]:
The final sample consisted of 10 participants (5 men and 5 women) who were second-generation graduate students from a predominantly White, midsized urban university in the Northeast. This sample size corresponds to the CQR method of recruiting between 8 and 12 participants (Hill et al., 1997). Regarding racial background, 5 identified as Asian/Pacific Islander, 3 identified as Hispanic, 1 identified as Caribbean, and 1 identified as White/Hispanic.

[. . .]

Physical Characteristics of True Americans

Seven participants reported that white skin, blonde hair, and blue eyes were the physical characteristics of a true American. Among these 7 participants, 6 participants mentioned White (n = 2), Caucasian (n = 3), or light skin (n = 1); 4 participants mentioned blonde hair (n = 2) or light hair (n = 2); and 4 participants mentioned blue eyes (n = 2) or light eyes (n = 2). For example, 1 Asian American male participant strongly associated being American with being White and believed that skin color was more important than other characteristics. He stated, “Being White is like a trump card, you can be like ignorant in politics and be White but more American than like a Black or Asian person.” Only 1 of the 7 participants who described White features also included gender. This Caribbean American man stated, “Definitely male, White umm, definitely male and White.” Only 2 of the 7 participants spoke of these features being part of a cookie-cutter or stereotypical American view of what is considered American.

[. . .]

These findings should be considered in light of recent research in the area of American identity. For example, Cheryan and Monin (2005) found that although Asian Americans felt as American as their White American counterparts, they also recognized that they were not perceived as such by other Americans. Thus, it is possible that although our participants may have felt American, as second-generation Americans and racial/ethnic minorities, they may also have recognized that they were not perceived to be as American as White European Americans and thus described features such as blonde hair and blue eyes.

[. . .]

Collectively, the results of our study indicated that being and feeling like a true American was complex and related to a number of individual and contextual factors. The complexity of participants' American identity definitions and negotiations is clearly evident in the results, in which four out of the six domains included categories that could be considered conceptual opposites: physical characteristics (White with blonde hair and blue eyes vs. diverse); beliefs and values (ethnocentrism vs. multiculturalism); impact of 9/11 (us-vs.-them mentality vs. greater unity); and participants' American identity (felt like a true American vs. did not feel like a true American). In addition, our results highlight the potential impact of sociopolitical forces in determining individuals' definitions and feelings of inclusion within a superordinate national identity.

[1] Park-Taylor et al. What It Means to Be and Feel Like a “True” American: Perceptions and Experiences of Second-Generation Americans. Cultural Diversity and Ethnic Minority Psychology. April 2008, Vol. 14, No. 2, p 128-137

Acceptance of anti-scientific Marxist brainwashing correlates with PC

Shocking:
J Pers Soc Psychol. 2008 Jun;94(6):1033-47.

Biological conceptions of race and the motivation to cross racial boundaries.
Williams MJ, Eberhardt JL.

Department of Psychology, University of California-Berkeley, Berkeley, CA 94720, USA. melissa@berkeley.edu

The present studies demonstrate that conceiving of racial group membership as biologically determined increases acceptance of racial inequities (Studies 1 and 2) and cools interest in interacting with racial outgroup members (Studies 3-5). These effects were generally independent of racial prejudice. It is argued that when race is cast as a biological marker of individuals, people perceive racial outgroup members as unrelated to the self and therefore unworthy of attention and affiliation. Biological conceptions of race therefore provide justification for a racially inequitable status quo and for the continued social marginalization of historically disadvantaged groups. (PsycINFO Database Record (c) 2008 APA, all rights reserved).

PMID: 18505316 [PubMed - in process]
More:
Human survival and well-being fundamentally depend on connections to other people. In the present research, we examine the extent to which people's conceptions of social groups determine which connections are most worthy of investment. Specifically, we investigate whether conceiving of racial group membership as biologically rooted determines to whom people attend and with whom they affiliate. We argue that a biological notion of race saps people's desire to reach out to members of racial groups that have been historically disadvantaged. These biological outgroup members ultimately are rendered, as a group and individually, less relevant to the self.

In the United States, race has traditionally been viewed in terms of biological essentialism—that is, race is understood to be a fundamental and stable source of division among humankind that is rooted in our biological makeup. More recently, however, some have come to see race as a social construct, initially created for purposes of maintaining a hierarchical social order but now a meaningful marker of cultural orientation, social identity, and experiences with discrimination (Smedley & Smedley, 2005).

[. . .]

The purpose of the present research is not to determine which view is most accurate but instead to investigate the consequences of endorsing one conception over another.

[. . .]

Less often have researchers investigated the role of people's evaluatively neutral beliefs in explaining reactions to racial disparities and the quality of interracial interactions. Beyond racial prejudice, in this article we investigate whether a simple belief that racial categories are biologically determined has the power to dampen people's motivation to engage with historically disadvantaged racial groups. Affiliating and engaging with others is a fundamental need. However, a biological conception of race may function as an affiliation cue that operates preferentially, such that people who hold this conception most desire to affiliate with those who are in their biological ingroup. That is, because people are more likely to direct their resources and attention to those whom they perceive as kin (Hamilton, 1964; Kruger, 2003; O'Gorman, Wilson, & Miller, 2005), they may direct their resources and attention to those within their racial ingroup when they view race as biological in nature.

We demonstrate in the present studies that individuals who understand race to be biologically derived are more accepting of racial inequities. They tend to understand racial inequities as natural, unproblematic, and unlikely to change (Study 1), a relationship that cannot be accounted for by racial prejudice. Moreover, an experimentally manipulated view of race as biological leads people to respond to racial inequities with less emotional engagement (Study 2). That is, they are not only less motivated to change racial inequities but also less concerned with and moved by such disparities. At the interpersonal level, we show that those with a biological conception of race maintain friendship networks that are less racially diverse (Study 3), have less desire to develop friendships across race lines (Studies 3 and 4), and are less interested in simply sustaining contact with a person of another race (Study 5) than are those with a social conception of race. Thus, we argue that a biological notion of race—beyond racial prejudice—sharpens associational preferences along race lines.

Some Evolution and Human Behavior abstracts/excerpts

doi:10.1016/j.evolhumbehav.2008.04.006

Consanguineous marriages: do genetic benefits outweigh its costs in populations with α+-thalassemia, hemoglobin S, and malaria?

Srdjan Denic et al.

Consanguinity is widespread in populations with endemic malaria. This practice, leading to an increase of homozygosis, could be either detrimental for lethal alleles (like hemoglobin S) or be potentially advantageous for beneficial alleles (like α+-thalassemia). The objective of this study was to analyze the effects of inbreeding on the fitness of a population with both, α+-thalassemia and hemoglobin S mutations. We calculated the relative fitness of an inbred population with α+-thalassemia and sickle cell anemia using a standard formula, and then compared it to that of an outbred population. An increase in the frequency of α+-thalassemia allele (0–1) results in a gain of relative fitness that is proportional to the coefficient of inbreeding; it is maximal at an allele frequency in the vicinity of 0.5. For hemoglobin S, an increase of frequency (0 to equilibrium point) produces a progressive loss of relative fitness that is also proportional to the coefficient of inbreeding; it is lowest at the equilibrium frequency that is always lower than 0.5. In a consanguineous population with both α+-thalassemia and hemoglobin S under selection pressure of malaria, the sum of contrary effects of inbreeding on the relative fitness of population depends on the frequencies of the two alleles and the coefficient of inbreeding.

Keywords: Consanguineous marriages; Inbreeding; Malaria; Thalassemia; Hemoglobin S; Relative fitness; Simulation model

[. . .]

Our findings provide a plausible hypothesis for explaining the confinement of consanguineous marriages to the tropical and subtropical regions where malaria is endemic and explain their absence in other parts of the World. As such, they complement the socioeconomic benefits theory of consanguinity ([Alwan and Modell, 1997], [Bittles, 2001] and [Khlat, 1997]). If consanguinity produces more surviving offspring (higher fitness) in some malarious populations, then a better protection of these survivors of malaria, as per socioeconomic theory of consanguinity, would further add to family fitness. Although neither theory is experimentally testable, the theoretical arguments underpinning both, as well as their complementing picture, will further insight into the causes and effects of customs regarding human reproduction.

doi:10.1016/j.evolhumbehav.2007.12.008

Correlated preferences for men's facial and vocal masculinity

David R. Feinberga et al.

Previous studies have reported variation in women's preferences for masculinity in men's faces and voices. Women show consistent preferences for vocal masculinity, but highly variable preferences for facial masculinity. Within individuals, men with attractive voices tend to have attractive faces, suggesting common information may be conveyed by these cues. Here we tested whether men and women with particularly strong preferences for male vocal masculinity also have stronger preferences for male facial masculinity. We found that masculinity preferences were positively correlated across modalities. We also investigated potential influences on these relationships between face and voice preferences. Women using oral contraceptives showed weaker facial and vocal masculinity preferences and weaker associations between masculinity preferences across modalities than women not using oral contraceptives. Collectively, these results suggest that men's faces and voices may reveal common information about the masculinity of the sender, and that these multiple quality cues could be used in conjunction by the perceiver in order to determine the overall quality of individuals.

Keywords: Face; Voice; Femininity; Hormonal contraceptive; Birth control; Pill


doi:10.1016/j.evolhumbehav.2008.06.002

Why do some dads get more involved than others? Evidence from a large British cohort

Daniel Nettle

Previous studies in developed-world populations have found that fathers become more involved with their sons than with their daughters and become more involved with their children if they are of high socioeconomic status (SES) than if they are of low SES. This paper addresses the idea proposed by Kaplan et al. that this pattern arises because high-SES fathers and fathers of sons can make more difference to offspring outcomes. Using a large longitudinal British dataset, I show that paternal involvement in childhood has positive associations with offspring IQ at age 11, and offspring social mobility by age 42, though not with numbers of grandchildren. For IQ, there is an interaction between father's SES and his level of involvement, with high-SES fathers making more difference to the child's IQ by their investment than low-SES fathers do. The effects of paternal investment on the IQ and social mobility of sons and daughters were the same. Results are discussed with regard to the evolved psychology and social patterning of paternal behaviour in humans.

Keywords: Fathers; Sons; Daughters; Socioeconomic status

[. . .]

As several previous studies in developed societies have also found ([Cabrera et al., 2000], [Harris et al., 1998], [Kaplan et al., 1998] and [Lawson & Mace, submitted for publication]), paternal involvement is patterned by SES and by sex of the child, with high-SES fathers more involved than low-SES ones, and sons receiving more paternal involvement than daughters. High paternal involvement is associated with significantly increased IQ scores at age 11 in this large British cohort, even when family SES and number of other siblings are controlled for. This result is consistent with previous findings for IQ and educational attainment measures from this (Flouri & Buchanan, 2004 E. Flouri and A. Buchanan, Early father's and mother's involvement and child's later educational outcomes, British Journal of Educational Psychology 74 (2004), pp. 141–153. Full Text via CrossRef | View Record in Scopus | Cited By in Scopus (17)Flouri & Buchanan, 2004) and other (Kaplan et al., 1998) cohorts.

[. . .]

This study shows for the first time an interaction effect with father's SES, with professional and managerial fathers making more difference to child IQ scores when they invest than unskilled fathers do (see Fig. 3). High-SES fathers may have more skills to enrich and improve the environment of the child's development than low-SES fathers do. As Kaplan et al. (1998) suggested might be the case, high SES fathers seem to be more efficient at embodying human capital in their children than low-SES fathers are. This gives a powerful potential explanation of why low-SES groups are characterised by low paternal effort. The returns to effort are low, and therefore men have no incentive for higher effort.

[. . .]

High-investing fathers did not have more grandchildren than low-investing fathers in this cohort. This does not necessarily mean that investment is not adaptive, since evolution favours strategies that maximise the contribution of the lineage to the population at an indefinitely far point in the future, and strategies can be adaptive even if their mean payoffs do not exceed the average for several generations (McNamara & Houston, 2006). High-investing fathers, especially from high SES backgrounds, did improve the quality and final social status of their children, and given that social status generally predicts marriage and fertility, at least for men (Fieder & Huber, 2007), it is quite plausible that they thereby reduce the risk of lineage extinction in the longer term. On the other hand, it may be that in this low-fertility, high parental investment, post demographic transition society, investment strategies that might have had an adaptive basis in ancestral environments have become decoupled from realised (grand)offspring numbers.


doi:10.1016/j.evolhumbehav.2008.03.003

Sexual coercion and life-history strategy

Paul R. Gladden

The present study evaluates three ultimate theories accounting for individual differences in sexually coercive tendencies: (1) Life History (LH) theory, (2) Competitively Disadvantaged Male theory, and (3) Sexual Coercion as a By-product theory. Three-hundred twenty-four college students completed questionnaires measuring LH strategy, perceived mate value, mating effort, short-term and long-term mating orientation, aggressive tendencies, psychopathy, and sexually coercive behavior. Eight tactical subscales extracted from the Sexual Acts and Perceptions Inventory converged upon one latent Sexual Coercion factor. The predictor variables clustered into a second Protective LH latent factor, which buffered Sexual Coercion. The Protective LH factor fully mediated the relation between sex and Sexual Coercion. Thus, the three evolutionary accounts of sexual coercion describe unique facets of a single LH trait rather than three dissociable alternatives. We discuss the conclusion that reproductive LH strategy partially underlies the variation in predisposition toward sexual coercion.

Keywords: Sexual coercion; Life-history theory; Sex differences; Social deviance; Aggression

[. . .]

4.1. LH strategy and social deviance

Ellis (1988) and others (e.g., Rushton, 1985) argue that a fast LH strategy underlies general criminality. Consistent with this view, we found that the short form of the Arizona LH Battery converged on the Protective LH factor with measures of socially deviant attitudes (e.g., aggression, psychopathy, machiavellianism), which served as inverse indicators of that factor. As noted above, LH strategies are composed of coordinated tactics. Our findings suggest that if men possess evolved specialized adaptations for sexual coercion, then sexual coercion may be one tactic among many subsumed by a general fast LH strategy, that is, a suite of tactics characterized by a diverse repertoire of socially deviant adaptive tactics. For example, if general social deviance is driven by fast LH strategies (e.g., [Ellis, 1988] and [Figueredo et al., 2006]), then sexually coercive individuals could be “criminal-generalists” (Malamuth et al., 2005 N. Malamuth, M. Huppin and B. Paul, Sexual coercion, The handbook of evolutionary psychology (2005), pp. 394–418.Malamuth et al., 2005), yet also be specialized to use sexual coercion as one of the tactics characteristic of their fast reproductive strategies. In short, sexual coercion could be one specialized adaptive tactic that contributed to the reproductive success of fast LH individuals in certain social contexts. One possibility is that fast LH strategies develop partly in response to self-assessments of low mate value and that these strategies are specialized for sexual coercion. Alternatively, sexual coercion may not have directly contributed to reproductive success but instead might be generated as a side effect of selection for fast LH traits that were under direct selective pressure such as interest in casual sex and risk-taking ([Palmer, 1991], [Symons, 1979] and [Thornhill and Palmer, 2000]).

[. . .]

To summarize, slow LH strategy, mate value, low mating-effort, a long-term sexual strategy, low psychopathy, low machiavellianism, and low aggression clustered into one common Protective LH factor that was negatively associated with a Sexual Coercion factor. The Protective LH factor fully mediated the relation between subject sex and Sexual Coercion. Therefore, Protective LH predictors co-occurred within individuals, indicating a single underlying construct that buffers individuals against using sexually coercive tactics. The LH view is consistent with either the idea that sexual coercion is a specific adaptation or that it is a by-product of traits adaptive for fast LH individuals ([Palmer, 1991], Thornhill and Palmer, 2000 R. Thornhill and C. Palmer, A natural history of rape: Biological bases of sexual coercion, MIT Press, Cambridge, MA (2000).[Thornhill and Palmer, 2000], [Thornhill and Palmer, 2004] and [Thornhill and Thornhill, 1992]). The Protective LH factor found in the present study must be replicated in other samples to support or refute the view that the three seemingly alternative evolutionary accounts describe different features of fast LH individuals.

IGF-1 levels correlate with SES

Annals of Epidemiology
Volume 18, Issue 8, August 2008, Pages 664-670
doi:10.1016/j.annepidem.2008.03.001

Social Differences in Insulin-like Growth Factor-1: Findings from a British Birth Cohort

Meena Kumaria et al.

Purpose

Insulin-like growth factor-1 (IGF-1) is related to factors that are socially patterned and may play a role in social differences in the development of morbidities including disability. Our aim is to examine whether there are social differences in IGF-1 in a cohort of participants between 44 and 45 years of age.

Methods

We examine the association of IGF-1 with social position measured by father's or own occupational class at three time points in childhood and adulthood, in a cohort of individuals born in one month in 1958 (N = 3,374 men and 3,302 women).

Results

Lower IGF-1 levels were associated with lower social position measured with father's occupational class at birth (p < 0.0001) and own occupational class aged 42 years (p < 0.001). Adult social position was associated with IGF-1 independently of social position at birth (p < 0.001) or any covariates examined. Conclusions IGF-1 secretion is associated with social position such that low social position is associated with lower levels of IGF-1. This biomarker may play a role in the development of social differences in morbidities associated with aging, such as the development of disability.

Key Words: Socioeconomic Status; Life Course; Inequalities in Health; Birth Cohort; Insulin-like Growth Factor–1

Abbreviations: IGF-1, insulin-like growth factor–1; BMI, body mass index; HbA1c, glycosylated hemoglobin

[. . .]

Insulin-like growth factor–1 (IGF-1) is an anabolic protein, related to insulin, which has important actions on cell division, metabolism, as well as on cell proliferation in vascular smooth muscle. Low levels of IGF-1 are associated with atherosclerosis and may be predictive of cardiovascular events (1), type 2 diabetes (2), loss of physical functioning (3), whereas high levels of IGF-1 are associated with the development of certain cancers (2).

[. . .]

Heart disease (1), diabetes (2), functioning, or disability (3) show associations with social position, and our findings suggest that IGF-1 may play a role in the pathways that mediate these differences. This is interesting in light of the recent increase in the prevalence of type 2 diabetes and in the context of an aging population with the resultant increases in disability and poor functioning. An independent association with disability may be mediated by IGF-1 because low IGF-1 levels may correspond to a decrease in the ability to maintain muscle mass (42). Further investigation into the predictors of high IGF-1 levels may help to identify predictors for the maintenance of muscle mass that may militate against the development of disability.

A related (?) finding from an older study:
Female facial attractiveness was best predicted by BMI and past health problems, whereas male facial attractiveness was best predicted by the socioeconomic status (SES) of their rearing environment.

[. . .]

Good genes theory predicts that variables contributing positively to individual health and fitness should be positively related to each other, and negatively related to variables that impact negatively on health and fitness. In this study, “positive” variables are SES and attractiveness, and “negative” variables are BMI, asymmetry and Health Problems. The results of between-variables correlations are thus generally consistent with good genes theory, although not all correlations were significant (Table 2).

Frequency of common alleles for deafness increasing

The American Journal of Human Genetics, 24 July 2008
doi:10.1016/j.ajhg.2008.07.001

A Comparative Analysis of the Genetic Epidemiology of Deafness in the United States in Two Sets of Pedigrees Collected More than a Century Apart

Kathleen S. Arnos et al.

Abstract

In 1898, E.A. Fay published an analysis of nearly 5000 marriages among deaf individuals in America collected during the 19th century. Each pedigree included three-generation data on marriage partners that included at least one deaf proband, who were ascertained by complete selection. We recently proposed that the intense phenotypic assortative mating among the deaf might have greatly accelerated the normally slow response to relaxed genetic selection against deafness that began in many Western countries with the introduction of sign language and the establishment of residential schools. Simulation studies suggest that this mechanism might have doubled the frequency of the commonest forms of recessive deafness (DFNB1) in this country during the past 200 years. To test this prediction, we collected pedigree data on 311 contemporary marriages among deaf individuals that were comparable to those collected by Fay. Segregation analysis of the resulting data revealed that the estimated proportion of noncomplementary matings that can produce only deaf children has increased by a factor of more than five in the past 100 years. Additional analysis within our sample of contemporary pedigrees showed that there was a statistically significant linear increase in the prevalence of pathologic GJB2 mutations when the data on 441 probands were partitioned into three 20-year birth cohorts (1920 through 1980). These data are consistent with the increase in the frequency of DFNB1 predicted by our previous simulation studies and provide convincing evidence for the important influence that assortative mating can have on the frequency of common genes for deafness.

[. . .]

Introduction

The importance of heredity as a cause of hearing loss has been recognized at least since the beginning of the 19th Century. For example, in 1857, the Irish otologist William Wilde concluded from an analysis of questions about deaf individuals in census data that parental consanguinity and the existence of deafness in one or both parents were important indicators of a hereditary etiology in some cases.1 In 1883, Alexander Graham Bell published a report titled Memoir upon the Formation of a Deaf Variety of the Human Race, which included a retrospective analysis of records from schools for the deaf in the United States.2 Bell expressed his concern about “the formation of a deaf variety of the human race in America,” based on analyses of the frequency of deaf relatives of deaf students and the hearing status of the offspring of marriages among those who were congenitally deaf compared to those who were adventitiously deaf. Bell argued that the use of sign language, the trend toward education in residential schools, and the creation of societies and conventions for deaf people restricted mating choices and fostered intermarriage, leading to a steady increase in the frequency of congenital deafness. Geneticists have generally discounted Bell's concerns once the extreme heterogeneity of genes for deafness was recognized; however, as described below, recent evidence suggests that, in combination with relaxed selection, assortative mating among the deaf population might in fact have preferentially amplified the commonest forms of recessive deafness.3

[. . .]

Because of the large number of recognized genes for deafness, the discovery that mutations at a single locus, DFNB1 (MIM 220290), account for 30%–40% of nonsyndromic deafness in many populations came as a great surprise.[12] and [13] DFNB1 includes the GJB2 (MIM 121011) and GJB6 (MIM 604418) genes, coding for the Connexin 26 (Cx26) and Connexin 30 (Cx30) subunits of homologous gap-junction proteins. These subunits are expressed in the inner ear, where they form heteromeric gap-junction channels between adjacent cells that permit the exchange of small molecules and may facilitate the recycling of potassium ions from the hair cells, after acoustic stimulation, back into the cochlear endolymph. More than 154 GJB2 mutations have been identified in the coding exon of GJB2, but a single chain-termination mutation, 35 del G, accounts for up to 70% of pathologic alleles in many populations. Although DFNB1 is common in Western Europe and the Middle East,[14] and [15] much lower frequencies have been observed in Asia.[16], [17] and [18] The 35 del G mutation exhibits linkage disequilibrium, and haplotype analysis suggests that it arose from a single individual in the Middle East approximately 10,000 years ago.[19] and 20 M. Tekin, N. Akar, S. Cin, S.H. Blanton, X.J. Xia, X.Z. Liu, W.E. Nance and A. Pandya, Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians, Hum. Genet. 108 (2001), pp. 385–389. Full Text via CrossRef | View Record in Scopus | Cited By in Scopus (27)[20]

[. . .]

In 2000, we proposed that the high frequency of DFNB1 deafness reflects the joint effect of intense assortative mating and the relaxed genetic selection against deafness, which occurred after the introduction of sign language 400 years ago in many Western countries and the subsequent establishment of residential schools for the deaf.29 Using computer simulation, we showed that this mechanism could have doubled the frequency of DFNB1 deafness in the United States during the past 200 years.3

Importance of the Mating Structure of the Population

Along with consanguinity, assortative mating is an important characteristic of a population that can have a profound influence on the incidence of deafness. When a new recessive mutation first arises, there is a substantial risk that it will be lost by stochastic processes. Consanguinity helps ensure that at least some recessive mutations are expressed phenotypically where they can be exposed to positive or negative selection. Only after genes for deafness are expressed can assortative mating accelerate their increase in response to relaxed selection. Consanguinity, of course, affects all recessive genes indiscriminately, but the effect of assortative mating among the deaf is limited to genes for deafness, in which it preferentially increases the frequency of the commonest form of recessive deafness in a population.3 Acting together, these genetic mechanisms can thus promote the survival, expression, and spread of genes for deafness. The acquisition of either a traditional or an indigenous sign language, especially when used by both deaf and hearing family members, is perhaps the most important factor that can improve the “genetic fitness” of the deaf population. Although their fitness was generally quite low in Europe prior to the time that sign language and schools for the deaf were introduced, it is now becoming apparent from a growing number of examples that a similar amplification of the frequency of specific genes for deafness can result from the development of indigenous sign languages that are used within extended families to allow deaf and hearing family members to communicate with one another.[30], [31], [32] and 33 T.B. Friedman, Y. Liang, J.L. Weber, J.T. Hinnant, T.D. Barber, S. Winata, I.N. Arhya and J.H. Asher, A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17, Nat. Genet. 9 (1995), pp. 86–91. Full Text via CrossRef | View Record in Scopus | Cited By in Scopus (94)[33] As a result of the integration of the deaf population into the community, the fitness of deaf individuals can be unimpaired in this setting, and when D × D marriages occur, virtually all are noncomplementary, as expected, because there is usually only one form of genetic deafness in the community. Although gene drift and endogamy undoubtedly play essential roles in the survival and initial phenotypic expression of genes in such populations, it is hard to escape the conclusion that relaxed selection and assortative mating must also contribute to the remarkable increases that can be seen in both gene and phenotype frequencies and to the strong evidence for a founder effect.

[. . .]

In the United States, 80%–90% of individuals with profound deafness currently marry a deaf partner;39 however, the introduction of cochlear-implant technology is profoundly altering the mating structure of the deaf population. By facilitating oral communication and educational mainstreaming, substantially all of the deaf children of hearing parents will be redirected into the hearing mating pool. Even if all of the deaf children of deaf parents eschewed implants, continued to learn sign language, and mated assortatively, the size of the pool would decrease dramatically and would be increasingly composed of individuals with DFNB1 mutations. Under these assumptions, the ultimate size at which the mating pool stabilizes might well be influenced by the extent to which genotypic mate selection replaces phenotypic selection in the interim (Nance et al., American College of Medical Genetics meeting 2006, San Diego, USA, Abstract 52). On the other hand, if deaf couples begin to embrace cochlear-implant technology for their children, the pool size will continue to decrease, eventually resulting in the substantial disappearance of the deaf culture. Thus, the collection and analysis of data on marriages of deaf individuals might represent a vanishing opportunity to understand the factors that have contributed to secular changes in the genetic epidemiology of deafness in this country since Fay's landmark study.

Neolithic population crash in Germany?

Journal of Archaeological Science
Volume 34, Issue 8, August 2007, Pages 1339-1345

Prehistoric population history: from the Late Glacial to the Late Neolithic in Central and Northern Europe

Stephen Shennan and Kevan Edinborough

Abstract

Summed probability distributions of radiocarbon dates are used to make inferences about the history of population fluctuations from the Mesolithic to the late Neolithic for three countries in central and northern Europe: Germany, Poland and Denmark. Two different methods of summing the dates produce very similar overall patterns. The validity of the aggregate patterns is supported by a number of regional studies based on other lines of evidence. The dramatic rise in population associated with the arrival of farming in these areas that is visible in the date distributions is not surprising. Much more unexpected are the fluctuations during the course of the Neolithic, and especially the indications of a drop in population at the end of the LBK early Neolithic that lasted for nearly a millennium. Possible reasons for the pattern are discussed.

Keywords: Mesolithic; Neolithic; Radiocarbon dates; Population history

[. . .]

In a recent paper Gamble et al. (2005) used the S2AGES database of radiocarbon dates for the period from c. 25–8 ka that they had compiled for western and northern Europe to propose an outline of the population history of the region during the Late Glacial period. The object of this paper is to follow up that study, albeit it on a more limited geographical scale, by adopting essentially the same approach to trace regional population histories in three areas of Central and Northern Europe up into the Neolithic, and in particular beyond the Neolithic transition on which earlier radiocarbon work by one of us was focussed (Gkiasta et al., 2003). In our view the results reveal some striking patterns which have significant implications for our understanding not just of the beginning of the Neolithic but more importantly what happened after it.

[. . .]

Starting with the earliest periods and working to the right, a number of features may be observed. In all cases the Mesolithic population shows fluctuations, but immediately before the beginning of the Neolithic it is actually lower than it was in some earlier phases. If one compares the maximum Mesolithic peak with the first Neolithic peak in each region, the Mesolithic peak in Denmark is proportionally the highest, which is likely to be a reflection of the significance of aquatic resources in Denmark and the high populations they are capable of supporting (cf. Schmölke, 2005). As noted above, while there may be some doubt about the comparability of the Mesolithic and Neolithic proxy population patterns, the bias against the former in favour of dates for the latter would have to be massive to alter the obvious inference to be made from the figure. The Danish pattern is basically the same as that produced in a similar radiocarbon exercise for Denmark and Sweden by Persson (1998, reproduced in Price, 2003). The beginning of the Neolithic is strikingly apparent in all three areas: the start of the LBK in Germany at c. 5500 cal BC, slightly later in Poland; and the beginning of the TRB Neolithic in Denmark at just after 4000 cal BC. In all cases there is a rapid rise in population to a ceiling; in Germany and Denmark this is basically maintained for some time; the marked dip in the Polish R_Combine data may or may not be a sampling artefact.

After 5000 cal BC the German data suggest a remarkable decline in population, to a fraction of its maximum LBK levels, lasting, with one or two fluctuations, until after 3500 cal BC. Poland shows a very similar picture although the decline is not as striking. In Denmark there is no such marked crash although there is a decline to just over half the maximum 3500 cal BC value at c. 3000 BC, roughly at the transition between the Middle Neolithic TRB and the Single Grave Culture. A slight upturn follows, with a more marked decline after 2500 BC. In Poland a sudden rise to a peak at 3500 BC is followed by a decline to a much lower level in the centuries after 3000 BC, corresponding to the various local Polish versions of the Corded Ware. Germany by contrast shows a rapid rise to a new population plateau at c. 3400 BC, maintained until 2500 BC, followed by a marked dip and then a rapid rise again at a time corresponding to the Bell Beaker culture and the beginning of the early Bronze Age. The pattern in the final centuries of the third millennium BC should be treated with some caution, since in southern Germany and Poland at least this is already the beginning of the Early Bronze Age, so it is possible that not all available dates have been included.

[. . .]

That the appearance of the LBK marked a major population increase in the areas where it is found is well established. What the data make clear is the extremely low levels of Mesolithic population prior to this arrival; the implication being that existing hunter-gatherer populations only made a significant contribution demographically, genetically and culturally to the extent that they were incorporated into the advancing LBK demographic wave.

However, the most significant result, we would argue, is the demonstration of the drastic demographic decline at the end of the LBK and the long subsequent period of relatively low population levels. Explaining the reasons for this now becomes a major issue. The decline suggested here on the basis of the radiocarbon evidence also fits in with an increasing number of indications from other sources that far from being the foundation of the subsequent Neolithic across large parts of central, northern and northwestern Europe, in some respects at least it actually left little trace. Thus, the recent ancient DNA study of LBK samples (Haak et al., 2005 W. Haak, P. Forster, B. Bramanti, S. Matsumura, G. Brandt, M. Tänzer, R. Villems, C. Renfrew, D. Gronenborn, K.W. Alt and J. Burger, Ancient DNA from the first European farmers in 7500-year-old neolithic sites, Science 310 (2005), pp. 1016–1018. View Record in Scopus | Cited By in Scopus (40)Haak et al., 2005) suggested that the most frequent mtDNA variant was one which is extremely rare in the region in modern populations. Archaeobotanical studies are also making it increasingly apparent that the LBK crop exploitation system was an unusual one which did not have any descendants (Coward et al., unpublished paper and Bakels, in press).

doi:10.1016/j.jas.2006.10.031

Distant European populations distinct in facial morphology (no shit?)

Polak mentioned this study in a comment at Dienekes. Nothing too surprising here, but it would be nice to see more efforts of this sort. This is an abstract of a poster from the 2007 AAPA conference (pdf):
Variation in facial features among European populations measured from 3D photographs.

D.K. Liberton1, B. McEvoy2, M. Bauchet1, C.A. Hill1, J.T. Richtsmeier1, T. Frudakis3, M.D. Shriver1.
1Department of Anthropology, Pennsylvania State University, 2Smurfit Institute of Genetics, Trinity College Dublin, 3DNAPrint Genomics, Inc.

The presence of craniofacial variation among continentally described groups has been documented. However, finer-scale phenotypic variation among populations has been more difficult to determine. The purpose of this study is to use three-dimensional images to evaluate if there are significant patterns of facial difference among European populations. Besides determining the extent of regional population differences in facial morphology, this work serves as a foundation for studies involving European genetic stratification and the detection of genes that determine facial features.

The study consists of 180 adult women, aged 18-35, from four geographically discrete European regions: Warsaw, Poland (N=45); Rome, Italy (N=45); Porto, Portugal (N=45); and Dublin, Ireland (N=45). Threedimensional photographs were acquired from faces using the 3dMDface imaging system. Three-dimensional landmark coordinate data were collected from using the 3dMD Patient software and were analyzed using Euclidean Distance Matrix Analysis. Pairwise comparisons between geographic regions were performed to determine patterns of significant differences in facial morphology among the four European populations.

Our results indicate that differences in female facial morphology are symmetrical and that population differences are localized to specific facial regions. This shows that there are statistically significant differences in facial morphology among European populations which can be mapped using coordinate data generated from three-dimensional photographs. Furthermore, these results suggest that morphological differences in facial features may likely be the result of genetic differentiation among European populations.

Supported by grants: Science Foundation of Ireland, Walton Fellowship

Rushton and genital size: one more time

J. Philippe Rushton asserts [1]:
Orientals are the most K, Blacks are the most r, and Whites fall in between. Being more r means: [. . .] more developed primary sexual characteristics (size of penis, vagina, testes, ovaries)
Rushton apparently has many convinced the above assertions are ironclad facts. They are not. Despite Rushton's sometimes selective presentation of evidence, what data exist (on "size of penis, vagina, testes") fail to consistently align with Rushton's Asian < White < African framework.

Penis size

Rushton claims [2]:

We averaged the ethnographic data on erect penis and found the means to approximate:
Orientals, 4 to 5.5 in. in length and 1.25 in. in diameter;
Caucasians, 5.5 to 6 in. in length and 1.5 in. in diameter;
blacks, 6.25 to 8 in. in length and 2 in. in diameter.
The numbers above are apparently lifted directly (or indirectly via Coon's Racial Adaptations) from a book by "A French Army Surgeon" ("Jacobus X" / Jacobus Sutor) published in 1898 (so much for "averages" of "the ethnographic data"; Rushton cites "A French Army Surgeon" as merely an "e.g." of "the ethnographic record", but Rushton's "ethnographic record" is apparently limited to the supposed observations of a single 19th-century individual).

The numbers given for blacks (ranging up to "8 in. in length" for population means) are implausible on their face, and no modern study of blacks comes close to supporting anything but the very low end of that suggested range.

A study of Nigerians (n=115) finds "mean [stretched] penile length was 13.37 cm [5.26 inches] with a median of 13 cm" [3]. Another study, on 320 Nigerians, finds "average [presumably flaccid] length of the penis (81.6 +/- 0.94 mm); circumference of the penis (88.3 +/- 0.02 mm)" [4].

The Kinsey data, which may be less than ideal but which are cited by Rushton both directly and indirectly, suggest any difference in mean penile dimensions between black and white men in America is measurable in fractions of an inch:
White males had an average flaccid penis length of 4.0 inches, whereas the average black male's detumescent member measured 4.3 inches. But when erect, the average white penis was 6.2 inches long, whereas the average black's was 6.3 inches--still longer, but not by much. (Average circumference for whites was 3.7 inches; for blacks, 3.8.)

When Rushton cites WHO condom standards in support of his theory, he is merely indirectly referencing the Kinsey data (plus a sample from Thailand, and one from Australia). WHO did no original research. Their sole "African" sample is the American black sample from Kinsey [7].

[Update: Rushton claims the WHO specify three condom sizes [1]:
The World Health Organization Guidelines specify a 49-mm-width condom for Asia, a 52-mm-width for North America and Europe, and a 53-mm-width for Africa.
I'd taken Rushton at his word here and had not bothered to check his WHO claim beyond determining that WHO did no original research on the subject (as stated above). In reality, it's clear from the guidelines that WHO specify exactly two widths [7]:
WHO specifies a width of 49 mm or 53 mm with a tolerance of ±2 for individual condoms and ±1 for the average of the lot.
The WHO don't make distinctions among Europe, Africa, and Asia, but between Asia and everyone else [7]:
Condoms are made in various widths. Based on studies in Australia, Thailand and the USA, and the experience of major agencies, the wider condoms (flat width 52-55 mm) will be preferred in Australia, Africa, Europe, Latin America, the Middle East and North America, and the narrower condoms (47-51 mm) will be preferred in several Asian countries (see Appendix III). Other widths are also made for small specialized markets.
Note: the ranges encompass tolerances in the specification; only two distinct widths are specified.]

Testes size

Rushton reviews most of the evidence of which I'm aware in his 1987 paper [2]:
Measurements taken from living subjects as well as those at autopsy, show the size of testes is twofold lower in Asian men than Europeans (9 g vs 21 g), a difference too large to be accounted for entirely in terms of body size (Diamond, 1986; Short, 1984). [. . .] Contrary to the general trend, Freeman (1934) observed that, at autopsy, American blacks had less heavy testes than American whites (13g vs 15g). [. . .] Subsequently Daniel, Fienstein, Howard-Peebles, and Baxley (1982) found no black-white difference in testicular volume among American adolescents, while Ajmani, Jain, and Saxena (1985) found larger scrotal circumference in Nigerians than Europeans (212.6 mm vs 195.1 mm or 8.37 in. vs 7.68 in.)
Strangely, by 2000, Rushton seems to have grown somewhat amnesiac [1]:
Race differences in testicle size have also been measured (Asians = 9 grams, Europeans = 21 g). This is not just because Europeans have a slightly larger body size. The difference is too large. A 1989 article in Nature, the leading British science magazine, said that the difference in testicle size could mean that Whites make two times as many sperm per day as do Orientals. So far, we have no information on the relative size of Blacks.
Rushton also conveniently ignores "A French Army Surgeon" where the latter's claim fails to line up with the former's theory:
In no branch of the human race are the male organs more developed than in the African Negro. I am speaking of the penis only and not of the testicles, which are often smaller than those of the majority of Europeans.

Vaginal size

Rushton claims (apparently again relying on "A French Army Surgeon"):
Women were proportionate to men, with Orientals having smaller vaginas and blacks larger ones, relative to Caucasians.
Modern studies fail to bear out this claim, which tends to further reduce the credibility of Rushton's 19th-century source. One study using MRI finds "[r]ace was not associated with any differences in measurements of vaginal dimensions" [5]. A different study finds [6]:
posterior cast length is significantly longer, anterior cast length is significantly shorter and cast width is significantly larger in Hispanics than in the other two groups and (2) the Caucasian introitus is significantly greater than that of the Afro-American subject.
Nor do the "Afro-American" subjects have deeper vaginas: "[a]verage rod lengths for Caucasians and Afro-Americans were 11.51 and 11.18 cm [. . .] significantly different as measured by t test" [6].

References

[1] Race, Evolution, and Behavior 2nd Special Abridged Edition (pdf)

[2] Rushton, J.P. & Bogaert, A.F. (1987) Race differences in sexual behavior: Testing an evolutionary hypothesis. Journal of Research in Personality 21(4): pp. 536-7 (link)

[3] Orakwe JC et al. Can physique and gluteal size predict penile length in adult Nigerian men? West Afr J Med. 2006 Jul-Sep;25(3):223-5. (link)

[4] Ajmani ML et al. Anthropometric study of male external genitalia of 320 healthy Nigerian adults. Anthropol Anz. 1985 Jun;43(2):179-86. (link)

[5] Barnhart KT et al. Baseline dimensions of the human vagina. Hum Reprod. 2006 Jun;21(6):1618-22. Epub 2006 Feb 14. (link)

[6] Pendergrass PB et al. Comparison of vaginal shapes in Afro-American, caucasian and hispanic women as seen with vinyl polysiloxane casting. Gynecol Obstet Invest. 2000;50(1):54-9. (link)

[7] WHO Global Programme on AIDS. Specification and Guidelines for Condom Procurement. Appendix VII, Regional or Ethnic Differences in Erect Penis Size. Geneva: WHO, 1995. (pdf)

Ancient Mongolian mtDNA

I'd be more interested in Y-DNA results from the same time and place, which might help support or refute the "Genghis Khan" Y signature claim. The unsurprising presence of European morphological features in some skeletons is perhaps attributable to admixture by Iranian speakers, which would also likely be detected in a Y-DNA analysis.
American Journal of Physical Anthropology; Published Online: 25 Jul 2008

Ancient DNA analysis of human remains from the upper capital city of Kublai Khan

Yuqin Fu et al.

Keywords
ancient DNA • mitochondrial DNA • human origins • China

Abstract
Analysis of DNA from human archaeological remains is a powerful tool for reconstructing ancient events in human history. To help understand the origin of the inhabitants of Kublai Khan's Upper Capital in Inner Mongolia, we analyzed mitochondrial DNA (mtDNA) polymorphisms in 21 ancient individuals buried in the Zhenzishan cemetery of the Upper Capital. MtDNA coding and noncoding region polymorphisms identified in the ancient individuals were characteristic of the Asian mtDNA haplogroups A, B, N9a, C, D, Z, M7b, and M. Phylogenetic analysis of the ancient mtDNA sequences, and comparison with extant reference populations, revealed that the maternal lineages of the population buried in the Zhenzishan cemetery are of Asian origin and typical of present-day Han Chinese, despite the presence of typical European morphological features in several of the skeletons. Am J Phys Anthropol, 2008. © 2008 Wiley-Liss, Inc.

[link]

Genetics of criminality

Press release:
In one of the first studies to link molecular genetic variants to adolescent delinquency, sociological research published in the August issue of the American Sociological Review identifies three genetic predictors--of serious and violent delinquency--that gain predictive precision when considered together with social influences, such as family, friends and school processes.

[. . .]

The three genetic polymorphisms that predict delinquency include:

1. the 30-base pair (bp) promoter-region with a variable number tandem repeat (VNTR) in the monoamine oxidase A (MAOA) gene,

2. the 40-bp VNTR in the dopamine transporter 1 (DAT1) gene and

3. the Taq1 polymorphism in the dopamine D2 receptor (DRD2) gene. MAOA regulates several brain neurotransmitters important in behavioral motivation, aggression, emotion and cognition (e.g., serotonin, dopamine, norepinephrine).
The paper:
The Integration of Genetic Propensities into Social-Control Models of Delinquency and Violence among Male Youths

Authors: Guo, Guang; Roettger, Michael E.; Cai, Tianji

Source: American Sociological Review, Volume 73, Number 4, August 2008 , pp. 543-568(26)

Abstract:
This study, drawing on approximately 1,100 males from the National Longitudinal Study of Adolescent Health, demonstrates the importance of genetics, and genetic-environmental interactions, for understanding adolescent delinquency and violence. Our analyses show that three genetic polymorphisms—specifically, the 30-bp promoter-region variable number tandem repeat (VNTR) in MAOA, the 40-bp VNTR in DAT1, and the Taq1 polymorphism in DRD2—are significant predictors of serious and violent delinquency when added to a social-control model of delinquency. Importantly, findings also show that the genetic effects of DRD2 and MAOA are conditional and interact with family processes, school processes, and friendship networks. These results, which are among the first that link molecular genetic variants to delinquency, significantly expand our understanding of delinquent and violent behavior, and they highlight the need to simultaneously consider their social and genetic origins.
My guess is genetic differences such as these (along with IQ) will ultimately be shown to account for a much larger fraction of cross-racial variation in crime than racial differences in circulating testosterone levels (which seem far from fixed). I don't have population frequency data for the specific polymorphisms mentioned above, but the SNP rs979606 in MAOA, for example, varies in the familiar Asian <> European <> African pattern. Update: Racial differences are also apparent in DRD2 Taq1 genotypes and the DAT1 40 bp VNTR, though their meaning is not clear to me yet.

Another relevant paper:
Neuropsychopharmacology (2008) 33, 425–430; doi:10.1038/sj.npp.1301417; published online 11 April 2007

A Non-Additive Interaction of a Functional MAO-A VNTR and Testosterone Predicts Antisocial Behavior

Rickard L Sjöberg et al.

Abstract

A functional VNTR polymorphism in the promoter of the monoamine oxidase A gene (MAOA-LPR) has previously been shown to be an important predictor of antisocial behavior in men. Testosterone analogues are known to interact with the MAOA promoter in vitro to influence gene transcription as well as in vivo to influence CSF levels of the MAO metabolite 3-methoxy-4-hydroxyphenylglycol (MHPG) in human males. We examined the possible joint effects of testosterone (measured in CSF) and MAOA-LPR genotype on antisocial personality disorder and scores on the Brown–Goodwin Aggression scale in 95 unrelated male criminal alcoholics and 45 controls. The results confirm that MAOA genotype and CSF testosterone interact to predict antisocial behaviors. The MAOA/testosterone interaction also predicted low levels of CSF MHPG, which tentatively suggests the possibility that the interaction may be mediated by a direct effect on gene transcription. If replicated these findings offer plausible explanations for previous inconsistencies in studies of the relationship between testosterone and male human aggression, as well as for how MAOA genotype may influence aggressive behavior in human males.
Keywords:

antisocial personality disorder, antisocial behavior, MAO-A gene, testosterone, gene by hormone interaction, MHPG

Confounding factors in 2D:4D studies

This tends to reinforce my doubts about the meaningfulness of direct comparisons of digit ratio across groups.

American Journal of Physical Anthropology; Published Online: 9 Jul 2008

Brief Communication: Latent toxoplasmosis and salivary testosterone concentration - Important confounding factors in second to fourth digit ratio studies

Jaroslav Flegr et al.

Keywords
infection • postnatal changes • Toxoplasma • androgens • 2D:4D

Abstract
A sexually dimorphic characteristic, the second to fourth digit ratio (2D:4D ratio), has been shown to reflect the prenatal concentration of sex steroid hormones and to correlate with many personality, physiological, and life history traits. The correlations are usually stronger for the right than the left hand. Most studies have shown that the 2D:4D ratio does not vary with age or postnatal concentration of sex steroid hormones. Recently, a strong association between left hand 2D:4D ratio and infection with a common human parasite Toxoplasma has been reported. We hypothesized that the confounding effect of Toxoplasma infection on left hand 2D:4D ratio could be responsible for the stronger association between different traits and right hand rather than left hand 2D:4D ratio. This confounding effect of toxoplasmosis could also be responsible for the difficulty in finding an association between 2D:4D ratio and age or postnatal steroid hormone concentration. To test this hypothesis, we analyzed the association between sex and age and 2D:4D ratio in a population of 194 female and 106 male students with and without controlling for the confounding variables of Toxoplasma infection and testosterone concentration. Our results showed that the relationship between age and sex and 2D:4D ratio increased sharply when Toxoplasma infection and testosterone concentration were controlled. These results suggest that left hand 2D:4D ratio is more susceptible to postnatal influences and that the confounding factors of Toxoplasma infection, testosterone concentration and possibly also age, should be controlled in future 2D:4D ratio studies. Because of a stronger 2D:4D dimorphism in Toxoplasma-infected than Toxoplasma-free subjects, we predict that 2D:4D ratio dimorphism as well as right hand/left hand 2D:4D ratio dimorphism will be higher in countries with a high prevalence of Toxoplasma infection than in those with a low prevalence. Am J Phys Anthropol, 2008. © 2008 Wiley-Liss, Inc.

[link]

Does not follow

Rienzi asserts, based on this study [1], that 'Personal "self-identification" is not enough. Genetic analyses of ancestry are required.' Rienzi clearly implies this study of "African Americans" indicates a need for individual genetic ancestry analysis of white Americans--an absurd conclusion.

Studies have repeatedly shown American blacks average ~20% European admixture, while white Americans show minimal if any non-European admixture. Gene flow was overwhelmingly one way.

It is no surprise that among American blacks "self-report of a high degree of African ancestry in a three-generation family tree did not accurately predict degree of African ancestry". The overwhelming majority of American blacks have "African" (black) parents and grandparents. No doubt most of Aframs' European genes entered the Afram gene pool more than 3 generation ago. Aframs without recent white ancestors may range from light-skinned to coal-black. We see no such variations in the phenotypes of white Americans.

Additionally, most white Americans who care to can construct pedigrees for themselves much deeper than three generations.

While I personally find genetic ancestry analysis interesting, and look forward to further developments in the field, as of now I see nothing of benefit for the overwhelming majority of white Americans in any commercially available test of individual admixture.


[1] Comparing genetic ancestry and self-described race in african americans born in the United States and in Africa. Yaeger R, Avila-Bront A, Abdul K, Nolan PC, Grann VR, Birchette MG, Choudhry S, Burchard EG, Beckman KB, Gorroochurn P, Ziv E, Consedine NS, Joe AK. Cancer Epidemiol Biomarkers Prev 2008;17(6):1329-38

More ancient DNA results from Xinjiang

I'm unfamiliar with the site and I haven't read the paper, but based on the dates mentioned (~500 BC to 1 AD) these results again most likely have little or no bearing on the question or the origins of the older, Northern European-looking mummies (which date to as early as ~1800 BC).

Sci China C Life Sci. 2008 Mar;51(3):205-13.

Mitochondrial DNA analysis of human remains from the Yuansha site in Xinjiang, China.

Gao S, Cui Y, Yang Y, Duan R, Abuduresule I, Mair VH, Zhu H, Zhou H.

Laboratory of Ancient DNA, Research Center for Chinese Frontier Archaeology, Jilin University, Changchun, 130012, China.

The Yuansha site is located in the center of the Taklimakan Desert of Xinjiang, in the southern Silk Road region. MtDNA was extracted from fifteen human remains excavated from the Yuansha site, dating back 2,000-2,500 years. Analysis of the phylogenetic tree and the multidimensional scaling (MDS) reveals that the Yuansha population has relatively close relationships with the modern populations of South Central Asia and Indus Valley, as well as with the ancient population of Chawuhu.

PMID: 18246308 [PubMed - indexed for MEDLINE]

Some ancient DNA results from the Tarim Basin

Note: some clown references this paper on Wikipedia in the following context:
The cemetery at Yanbulaq contained 29 mummies which date from 1800–500 BC, 21 of which are Caucasoid—the earliest Caucasoid mummies found in the Tarim Basin—and eight of which are of the same Caucasoid physical type found at Qäwrighul.[1]:237 . However, more recent genetic studies painted a more complex picture (Xie et al., 2007). It showed both european and asian characteristics.

In fact, this study has no bearing on the origins of the Northern Europoid "Tarim mummies". Sampul is a much later site, which according to physical anthropologists was populated primarily by Central Asian "Eastern Mediterranean" types. Mallory and Mair discuss the findings of Han Kangxin:
The Qäwrighul remains are relatively homogeneous and they exhibit features associated with a type known as Proto-Europoid, a rather robust Caucasoid, especially well represented in Northern Europe and the steppelands and forest-steppe of Russia and the Ukraine. Similar remains occur in the Bronze Age cemeteries of southern Siberia, Kazakhstan, Central Asia and the Lower Volga. [. . .]

The next oldest remains derive from the Yanbulaq cemetery near Humul (Hami), situated to the northeast of Qäwrighul and the easternmost cemetery investigated. Here Han Kangxin identified 21 of the 29 complete skulls as Mongoloids and these are the earliest definite evidence of Mongoloids in East Central Asia. The remaining skulls, however, belonged to Caucasoids who are closest to those from Qäwrighul and point to the same general direction for their origins, i.e. the steppelands to the north and west.

The single skull recovered from among the inhumation burials at Shambalay near Tahkurgan in the far west of the Tarim Basin has been compared with the type that spanned the Mediterranean across Central Asia; this type also includes the Saka tribes of the southern Pamirs.

A much larger sample of 58 skulls was recovered from one of the mass graves at Alwighul in the Tangri Tagh (Tian Shan). Here Han distinguishes two Caucasoids types: the Eastern Mediterranean or Indo-Afghan type with their long and high skulls and the broader and rounder skulls of the Pamir-Ferghana type; Han also identified hybrids of these two subtypes as well as some evidence of Mongoloid admixture. By now, the attentive reader will know we owe another caveat; the three physical types employed by Han Kangxin -- Proto-Europoids, Indo-Afghans and Pamir-Ferghanans -- are largely relabelled Nordics, Mediterraneans, and Alpines, terms that send shivers of apprehension down the spines of Western biological anthropologists.

[. . .]

The Sampul cemetery provides us with our only physical anthropological evidence of the southern Silk Road in the vicinity of Khotan. Although the cemetery contained various individual graves employing some form of log coffin, all the burials examined derive from the group graves which date to the first centuries BC. Han Kangxin has identified the remains as belonging to the same Indo-Afghan type that one encounters among the Saka of the southern Pamirs.

[pp. 236-239; The Tarim Mummies]



Progress in Natural Science, Volume 17, Number 8, pp. 927-933(7)

Mitochondrial DNA analysis of ancient Sampula population in Xinjiang

Xie Chengzhi Li Chunxiang Cui Yinqiu Cai Dawei Wang Haijing Zhu Hong Zhou Hui

Abstract: The archaeological site of Sampula cemetery was located about 14 km to the southwest of the Luo County in Xinjiang Khotan, China, belonging to the ancient Yutian kingdom. 14C analysis showed that this cemetery was used from 217 B.C. to 283 A.D. Ancient DNA was analyzed by 364 bp of the mitochondrial DNA hypervariable region I (mtDNA HVR-I), and by six restriction fragment length polymorphism (RFLP) sites of mtDNA coding region. We successfully extracted and sequenced intact stretches of maternally inherited mtDNA from 13 out of 16 ancient Sampula samples. The analysis of mtDNA haplogroup distribution showed that the ancient Sampula was a complex population with both European and Asian characteristics. Median joining network of U3 sub-haplogroup and multi-dimensional scaling analysis all showed that the ancient Sampula had maternal relationship with Ossetian and Iranian.

Keywords: ancient DNA mitochondrial DNA Sampula ancient populations

[link]

The authors detect the following haplogroups: U3 (in four individuals), N (x2), C (x2), B, F1a, G, M, and T2.

Oceania: tracing population history and adaptation with genome-wide SNP data

MBE Advance Access published online on June 3, 2008
Molecular Biology and Evolution, doi:10.1093/molbev/msn128

Gene Flow and Natural Selection in Oceanic Human Populations, Inferred from Genome-wide SNP Typing

Ryosuke Kimura1,*, Jun Ohashi2, Yasuhiro Matsumura3, Minato Nakazawa4, Tsukasa Inaoka5, Ryutaro Ohtsuka6, Motoki Osawa1 and Katsushi Tokunaga2

It is suggested that the major prehistoric human colonizations of Oceania occurred twice, namely, about 50,000 and 4,000 years ago. The first settlers are considered as ancestors of indigenous people in New Guinea and Australia. The second settlers are Austronesian-speaking people who dispersed by voyaging in the Pacific Ocean. In this study, we performed genome-wide SNP typing on an indigenous Melanesian (Papuan) population, Gidra, and a Polynesian population, Tongans, by using the Affymetrix 500K assay. The SNP data were analyzed together with the data of the HapMap samples provided by Affymetrix. In agreement with previous studies, our phylogenetic analysis indicated that indigenous Melanesians are genetically closer to Asians than to Africans and European Americans. Population structure analyses revealed that the Tongan population is genetically originated from Asians at 70% and indigenous Melanesians at 30%, which thus supports the so-called "Slow train" model. We also applied the SNP data to genome-wide scans for positive selection by examining haplotypic variation, and identified many candidates of locally selected genes. Providing a clue to understand human adaptation to environments, our approach based on evolutionary genetics must contribute to revealing unknown gene functions as well as functional differences between alleles. Conversely, this approach can also shed some light onto the invisible phenotypic differences between populations.

Key Words: adaptive evolution • gene flow • human genome • SNP • Oceania

http://mbe.oxfordjournals.org/cgi/content/short/msn128v1?rss=1

Isotopic analysis of an LBK mass grave

The Telegraph reports the study as follows:
Neolithic men were prepared to fight for their women

[. . .]

Many archaeologists have argued that women have long motivated cycles of violence and blood feuds throughout history but there has really been no solid archaeological evidence to support this view.

Now a relatively new method has been used to work out the origins of the victims tossed into a mass grave of skeletons, and so distinguish one tribe from another, revealing that neighbouring tribes were prepared to kill their male rivals to secure their women some 7000 years ago.

The Durham University research, described in the academic journal Antiquity, focused on 34 skeletons found buried in the village of Talheim in the south-west of Germany.

[. . .]

Lead author Dr Alex Bentley says the simplest explanation is that the women of one tribe were captured.

"It seems this community was specifically targeted, as could happen in a cycle of revenge between rival groups. Although resources and population were undoubtedly factors in central Europe around that time, women appear to be the immediate reason for the attack.

"Our analysis points to the local women being regarded as somehow special and were therefore kept alive."

Antiquity

Volume: 82 Number: 316 Page: 290–304

Isotopic signatures and hereditary traits: snapshot of a Neolithic community in Germany

R. Alexander Bentley1, Joachim Wahl2, T. Douglas Price3 and Tim C. Atkinson4

1Department of Anthropology, Durham University, 43 Old Elvet, Durham DH1 3HN, UK (Email: r.a.bentley@durham.ac.uk) 2RP Stuttgart, Landesamt für Denkmalpflege, Osteologie, Stromeyersdorfstraße 3, D-78467, Konstanz, Germany (Email: Joachim.Wahl@rps.bwl.de) 3Department. of Anthropology, University of Wisconsin, 1180 Observatory Dr., Madison, WI 53706-1393, USA (Email: tdprice@wisc.edu) 4Department of Earth Sciences, University College London, Gower Street, London WC1E 6BT, UK (Email: t.atkinson@ucl.ac.uk)

A group of Linearbandkeramik people at Talheim, Germany were previously found to have died at the same time, probably in a massacre, and the authors were able to ask some searching questions of their skeletons. The isotope signatures of strontium, oxygen and carbon, which gave information on diet and childhood region, showed up three groups which correlated with hereditary traits (derived previously from the analysis of the teeth). In the local group, there were many local children but no adult women, suggesting they had been selectively taken alive at the time of the massacre. Another group, with isotope signatures derived from upland areas, includes two men who may have been closely related. A third group has a composition suggestive of a nuclear family. The variations of one type of isotope signature with another suggested subtle interpretations, such as transhumance, and a probable labour division in the community between stockholders and cultivators. Here we see the ever-growing potential of these new methods for writing the ‘biographies’ of prehistoric skeletons.

Keywords: Neolithic, Germany, LBK, Talheim, isotope analysis, hereditary traits, trans-humance

http://www.antiquity.ac.uk/ant/082/ant0820290.htm

Hydraulic cement: Thank the English, not the Romans

[re: hysterical Medocentrist outburst elsewhere]

Portland cement as widely used today was originally formulated by Englishman William Aspdin, building on the work of other Englishmen, including his father Joseph Aspdin and, ultimately, John Smeaton:
Smeaton investigated the cementing properties of various mortars, made from lime obtained from various locations, and discovered that the best mortars were made from the calcination of limes that contained considerable proportions of clay minerals (argillaceous lime). This was the first occasion that the importance of clay mixed with the lime had been recognized in the formation of a hydraulic setting cement. It was found that limes that did not dissolve completely in nitric acid (clay being insoluble in the acid) possessed good hydraulic properties (Kohlhaas, 1983). The cementitious agent Smeaton finally used was made from such a clay containing lime which was mixed with an equal quantity of pozzolana (Lea, 1970). The lighthouse that he constructed stood for 123 years until 1879 and only failed when its foundations were undermined by the sea. Smeaton's conclusions about the importance of the presence of clay were not published until after his death in 1792. Smeaton was the first to call himself a civil engineer (as distinct from a military engineer). In the preface to his book, Hydraulischen Moertel, W Michaelis stated in 1869 (in translation):
A century has elapsed since the famous Smeaton completed the building of the Eddystone Lighthouse. Not only the seafaring but for all humanity stands as a true signal of blessed work, a light in the dark night. From the scientific point of view it illuminated the darkness of nearly 2000 years.

The errors which came to us from the Romans and which were shared even by the excellent Belidor, were dispersed.

The Eddystone Lighthouse is the foundation upon which our knowledge of hydraulic mortars has been built and is the chief pillar of modern construction. Smeaton freed us from the shackles of tradition by showing us that the purest and hardest limestone is not the best, at least for hydraulic purposes, and that the source of the hydraulicity of lime mortar must be sought in the argillacrious admixtures (Draffin, 1976).
The cement was called 'Roman cement' although it in no way resembled the true Roman cement, except for its hydraulic setting reactions.

[Mary S. J. Gani; Cement and Concrete; p. 5]


The Romans ceased building with high-quality concrete by around A.D. 300. Our modern knowledge of cement owes nothing to them.
Cement was used from the decline of the Empire and through the Middle Ages, but none of it was any good until comparatively recent times (Davey, 1961). [. . .]

In this case, it was not that a Roman secret was lost, rather that the Romans, who did no testing, never learned what they had. The very idea of testing is comparatively recent, and the engineer John Smeaton, who tested samples for the construction of the Eddystone Light in the years 1756– 1759 (Davey, 1961) is, I suspect, the first man on the planet deliberately to test cements of differing compositions.

[Thomas Nelson Winter. Roman Concrete: The Ascent, Summit, and Decline of an Art. Transactions of the Nebraska Academy of Sciences 7 (1979), pp. 137-143.]