Welcome to SALMON the 1998 UCISA award winning website developed by Dr Paul Kenyon (retired) to support students studying evolutionary psychology and behavioral neuroscience in the Department of Psychology, University of Plymouth, Devon, UK
The contents of this lecture should surprise and, I hope, interest you.
The heart of the lecture is a section describing two opposing views on
the development of gender.
Gender consists of three elements:
The widely held view that gender is the result of the nurture we receive as children is contrasted with the idea that gender is influenced with biological factors in our nature. The lecture explores some evidence that supports the latter position.
A series of experiments showing that it is possible to effect the sexual behaviour of animals by manipulating hormones circulating in their bodies during early development is presented.
An important message from these studies is that the mammalian brain and external genitalia tend to develop as female unless they are exposed to androgens in infancy.
This finding has important implications for human development which are
explored by presenting a study that suggests that girls that are exposed
to testosterone in utero exhibit masculine behaviour patterns in adulthood.
Sex is a biological term which refers to the functional differences between males and females and their reproductive potential
Gender is a psychological term which refers to our awareness and reaction to biological sex
Gender consists of several elements:
There are two fundamentally different explanations for how gender develops.
Many psychologists believe that gender is the result of environmental
influences, particularly the way we are treated by our parents, guardians,
friends and relatives. According to Dr John Money we are psychosexually
neutral at birth, and our gender is a consequence of the nurture we receive
as children.
A less popular view is that gender is the result of nature, particularly the effects of hormones on the developing brain.
This is not a dry academic argument. The lives of a significant number of people have been changed as a result of the application of these theories.
Point to ponder:
How do you think theories of gender development might have influenced the way parents raise their children?
This web page describes some of the evidence that suggests that gender may the result of exposure to hormones in the first few weeks of life.
Prenatal exposure to androgen could influence the development of gender role behaviours - behaviours that are typical of one or the other sex e.g. boys playing with construction toys; girls playing with dolls
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Berenbaum (1999) has shown clear differences in activities and job interests between adolescent boys and girls.
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Here is some unpublished data collected by Corrine Hutt (University of Reading, UK) who observed aggressive behaviour in pre-school children in a nursery situation.
She found that overall boys were more aggressive than girls; most aggressive acts tended to involve boys fighting with other boys. The amount of aggression by boys directed towards girls and vice versa tended to be relatively low.
Corrine argued that this sex difference in aggression was due to masculinization of the brain by testosterone
Perhaps the first question asked by parents and relatives after a child is born is "What sex is the child?". According to the nurture view of psychosexual differentiation this is the point at which shaping the child's gender identity begins. But the process may have started many weeks before when the baby was developing in the mother's womb. This series of diagrams shows how the development of a child's external genitalia is affected by exposure to the androgen dihydrotestosterone.
An important message from this diagram is that - regardless of genetic sex -
In early intrauterine development male and female external genitalia (visible sex organs) are identical.
Under the influence of the androgen dihydrotestosterone, the external genitalia develop in the male direction. In the absence of androgens female external genitalia develop.
The crucial point about this diagram is that tissues that are equivalent for the two sexes in the undifferentiated state will become different organs by the time of birth. You can follow this change by tracing the fates of the different coloured tissue. The top diagram shows the undifferentiated state. The middle diagrams shows differentiation beginning during the third and fourth months of pregnancy. The bottom diagrams show complete differentiation of the external genitalia at birth.
These diagrams are based on the drawings found in most textbooks that cover the the biological bases of sexual behaviour.
Androgens govern the development of human external genitalia. Exposure to androgens beginning around the eighth week of pregnancy causes undifferentiated tissue to develop in the male form. In the absence of androgens development is in the female form. This effect is independent of the genetic sex of the fetus. Animator: Dr Paul Kenyon
Androgens govern the development of human external genitalia. Exposure to androgens beginning around the eighth week of pregnancy causes undifferentiated tissue to develop in the male form. In the absence of androgens development is in the female form. This effect is independent of the genetic sex of the fetus. Animator: Dr Paul Kenyon
The nature and nurture views of psychosexual development differ in the significance they attach to the importance of hormones in the development of behavioural differences between males and females.
Hormones have two fundamentally different effects on sexual behaviour:
Organizational effects refer to the effects of hormones during the early development of an animal
Activational effects refer to the effects of hormones in the adult organism
There is evidence that exposure to hormones during a critical period of development changes the way in which the organism reacts to hormones in adulthood. Notice that this does not mean that early exposure to hormones has a permanent effect on behaviour. Instead it suggests that exposure to hormones in infancy affects how the adult reacts to hormones. In other words, early exposure to hormones organizes the way behaviour is activated by hormones in adulthood. We need to spend a few moments reviewing how the activational effects of hormones on behaviour are measured. Hormones such as testosterone, estrogen and progesterone, activate sexual behaviour of adult male and female rats
There is evidence that exposure to hormones during a critical period of development changes the way in which the organism reacts to hormones in adulthood.
Notice that this does not mean that early exposure to hormones has a permanent effect on behaviour. Instead it suggests that exposure to hormones in infancy affects how the adult reacts to hormones. In other words, early exposure to hormones organizes the way behaviour is activated by hormones in adulthood.
We need to spend a few moments reviewing how the activational effects of hormones on behaviour are measured. Hormones such as testosterone, estrogen and progesterone, activate sexual behaviour of adult male and female rats
Many studies measure female sexual behaviour in terms of 'lordosis'. Lordosis refers to a characteristic posture in which the female rodent arches her back and moves her tail to permit penetration by the male.
Sexual behaviour in male rats consists of three behaviours:
The activational effects of hormones are discussed in greater detail on a separate page of this website.
This page focusses on the organizational effects of hormones.
According to the nature theory of psychosexual differentiation, hormones organize the brain during development. In a nutshell:
The organizational effects of the presence or absence of testosterone are only apparent in adulthood when the organism is under the activational effects of testosterone or estrogen and progesterone.
Exposure to testosterone between about day 17 of gestation to day 8-10 of postnatal life organizes the brain of a male rat to determine how it will react to hormones in adulthood.
If a male rat is castrated at birth, and then given an injection of estrogen in adulthood, it exhibits lordosis, - a female sexual response - when tested with a sexually vigorous male rat.
If a male rat is castrated at birth, and then exposed to a female rat which is in estrus (heat) he will not mate with her.
In contrast, if a normal male is injected with estrogen in adulthood it does not display the lordosis response in the presence of a sexually vigorous male rat. A normal male rat will mate with a female rat in estrus.
Testosterone is thought to establish male circuits (masculinization),
and inhibit the development of female brain circuits (defeminization).
The absence of testosterone organizes the brain of a female rat to determine how it will react to hormones in adulthood.
If a female rat is injected with testosterone during infancy, and then given an injection of testosterone in adulthood, she will show male sexual responses - mount, intromission and ejaculation behaviours - when tested with a female rat in estrus.
If a female rat is injected with testosterone during infancy, and then injected with estrogen in adulthood, she will not exhibit lordosis behaviour when she is tested with a sexually vigorous male rat.
In contrast, if a normal female rat is injected with testosterone in adulthood, she will not exhibit male sexual behaviours.
A normal female rat in estrus will exhibit lordosis when paired with a sexually vigorous male rat.
Testosterone is thought to establish male circuits (masculinization), and inhibit the development of female brain circuits (defeminization).
In the absence of testosterone brain circuits are feminized and demasculinized.
Adult sexual behavior in the rat depends on whether the brain was organized by gonadal hormones during the first few days after birth.
Normal adult males display mounting behavior because their brains were subjected to a dose of testosterone from the gonads just after birth. The same effect can be produced in females by injecting the hormone testosterone.
Depriving male pups of testosterone by castrating them at birth results
in a female brain organization. As adults these feminized males, like normal
females, display very few attempts to mount, but a high frequency of lordosis
when mounted.
The DNA in a cell's nucleus is essentially a set of plans. The plans contain instructions that allow a cell to manufacture proteins. Steroid hormones exert powerful effects on the growth and specialization of cells. When hormones enter a cell's nucleus they open up its set of plans, and set protein manufacture in motion. (See Becker et al, 2002, p32-34)
Hormones travel through the cell membrane and bind with intracellular
steroid receptors. This hormone-receptor complex then passes into the nucleus
where it activates mRNA transcription which leads to the production of
proteins. The resulting proteins then leave the nucleus and pass into the
cell cytoplasm.
This picture shows the process:
When testosterone travels across the cell membrane it is converted into
estrogen by the enzyme aromatase. The estrogen attaches to a receptor which
takes it into the cell's nucleus where it initiates the production of proteins
based on instructions in the cell's DNA.
It is the expression of this genetic information which is responsible for masculinization.
Thus, in order to masculinize the brain the 'male' steroid hormone testosterone
must be converted into the 'female' hormone estrogen. You should read this
sentence again. It contains a paradox. It is saying that a 'female' hormone
is responsible for producing a male brain.
You might wonder if estrogen - produced by the mother's ovaries during
pregnancy - would cause masculinization of a female fetus. But in females
alphafetoprotein captures estrogen so that it cannot cross the cell membrane
and androgenise the female brain.
It is possible to masculinize the brain and behaviour of female rats by injecting them with such a large dose of estrogen that it overwhelms the alphafetoprotein estrogen-binding mechanism. Consequently the 'female' hormone estrogen can also masculinize brain and behaviour. (See Becker et al, 2002, p87-89)
The following account of the aromatization hypothesis is adapted from Milgram.
"The aromatization hypothesis is an attempt to explain how brain masculinization is caused by high levels of estrogen, which affect estrogen receptors in brain cells. According to the aromatization hypothesis, masculinization of some brain structures results from the conversion of testosterone to estrogen by an aromatase enzyme (aromatization). This hypothesis was originally proposed to account for the findings that:
- high levels of estrogen act like testosterone in leading to defeminization; and
- dihydroxytestosterone does not mimic the effect of testosterone.
Testosterone and dihydroxytestosterone differ in their response to aromatase enzyme; only testosterone is converted to the aromatic compound estrogen. Thus, dihydroxytestosterone does not produce defeminization.
If this hypothesis is correct, why aren't the brain of young females, who secrete estrogen, masculinized? One reason may be that ovarian secretion of estrogens are lower than testicular secretion of testosterone. Another factor that serves to prevent the aromatization of estrogen is a protein known as alpha-fetoprotein, which binds to estrogens but not testosterone and restricts the access of estrogens to estrogen receptors in the brain. This suggestion is supported by evidence of high levels of alpha-fetoprotein in young female rodents."
A number of behaviours in rats are effected by testosterone exposure around birth. These include:
Exploratory behaviour is more extensive among female rats than among male
rats. This behaviour is modified when female rats are injected with testosterone
shortly after birth. The bar chart shows the frequency of defecation, which
is inversely proportional to exploration, during a three minute open-field
test. When the females had not been injected with testosterone after birth
(left and centre groups) their boli count was significantly less than males.
Females that had been masculinized defecated at the same rate as males.
We have already describedhow androgen masculinizes the external genitalia of a developing baby.
Sometimes female embryos are exposed to abnormally high levels of androgen before birth. A small number of genetic females are born with ambiguous external genitalia. The most common cause of female pseudohermaphroditism is congenital adrenal hyperplasia (CAH) which occurs in about 1 in 5,000 to 15,000 live births. Congenital adrenal hyperplasia (CAH) also known as the adrenogenital syndrome (AGS).
CAH is a disease that affects the manufacture of the "stress" hormone, cortisol. Cortisol is released into the blood stream from the adrenal gland, a small organ near the kidney.
The diagram shows how a deficit in cortisol release disrupts the normal negative feedback between cortisol and ACTH secretion from the pituitary gland.
In CAH patients a metabolic error causes overproduction of androgens (e.g. testosterone) in the adrenal gland. This androgen leads to partial masculinization of the external genitalia of female patients which is corrected surgically at birth and with artificial cortisol supplements.
A great deal of attention has been given to the consequences of excess androgens on the psychosexual differentiation of these children.
We will examine some early psychological studies of these girls (Ehrhardt,
1975) which suggests that exposure to androgen during development causes
a partial masculinization of human female behaviour.
This picture shows a baby girl born with congenital adrenal hyperplasia (CAH) . Her external genitalia have been partially masculinized (virilized) as a result of exposure to high levels of testosterone whilst in the womb.
Ehrhardt (1975) studied 17 female CAH patients: age 4.3 to 19.9 years, most of the girls were in middle childhood and early adolescence. The comparison sample (n=11) consisted of the girls' sisters who did not have CAH.
All the patients were under long-term corrective treatment with replacement cortisol and had undergone surgical correction of the external genitalia, usually in infancy or early childhood.
Interviews with children and their mothers, fathers and siblings were tape-recorded. Interview transcripts were rated according to coded scales to elicit information about the child's behaviour.
Girls with CAH were more often described as having high levels of energy expenditure compared to their unaffected siblings.
They also tended to prefer to play with boys rather than other girls.
Although they tended to start fights more frequently than their sisters, this difference was not statistically significant.
This diagram shows that girls with CAH were not very interested in playing with dolls, instead they tended to play with cars, trucks and blocks; toys that are generally preferred by boys.
They showed little interest in future roles as brides or mothers, but were much more concerned with their careers.
Their relatives described them as being indifferent to - or avoiding - contact with babies. For example, they did not participate in caring for infants at home or go out baby-sitting.
Relatives and girls with CAH describe themselves as 'tomboys' during all of their childhood.
35% of the sample were unsure or said that they might have chosen to be a boy if they could start their lives over again. However, Ehrhardt points out that none of the girls were unsure about their gender identity. They did not feel that they were boys and being a girl did not make them unhappy. In other words - as a group - they did not exhibit gender dysphoria.
Conclusion: CAH appears to have a significant effect on gender role behaviours. Patients exhibit significantly more male-typical behaviours than unaffected siblings.
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According to a nature view of psychosexual differentiation, prenatal exposure to androgen could influence the development of gender identity - the feeling an individual has of being a man or a woman. In contrast the nurture position holds that we are psychosexually neutral at birth and that socialization is responsible for the development of gender identity.
In 1972 Money and Ehrhardt reported the case of a 7 month old baby boy - one of a pair of twins - born in 1963 whose penis was removed after an operation for circumcision damaged the child's penis. At 22 months old the child was surgically reassigned as a girl and brought up according to the prevailing view at the time that we are psychosexually neutral at birth. This case entered the textbooks and informed medical opinion for several decades because Money reported that the child had adapted well as a girl. But long term follow up of this case by Milton Diamond paints a very different picture of the success of this application of the nature theory of psychosexual differentiation.
"This article is a long-term follow-up to a classic case reported in paediatric, psychiatric, and sexological literature. The penis of an XY individual was accidentally ablated and he was subsequently raised as a female. Initially this individual was described as developing into a normally functioning female. The individual, however, was later found to reject this sex of rearing, switched at puberty to living as a male, and has successfully lived as such from that time to the present. The standard in instances of extensive penile damage to infants is to recommend rearing the male as a female. Subsequent cases should, however, be managed in light of this new evidence."
The story of a boy who was raised as a girl seems to show that gender really is all in the genes. Despite the efforts of psychiatrists, surgeons and parents, he never felt happy as a girl and eventually reverted to being a man, got married and is now living happily.The man's life history is told as a cautionary tale by Milton Diamond, a sexologist at Hawaii University in Archives of Paediatric Adolescent Medicine. He says that it is the first long-term follow-up of a male with the normal allotment of XY chromosomes who was raised as a female.
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Dr Diamond says that the problems for "John" began when he was eight months old, in 1963. An accident during circumcision left him without a penis. His parents took him to Johns Hopkins University in Baltimore, Maryland, where experts said that the best thing would be to raise him as a girl.
His testicles were surgically removed and an artificial vagina created, as is done in sex-change operations. John became Joan.
The result, says Dr Diamond, has often been extolled as the classic demonstration of how the environment can override nature in forming gender identity. In fact, he says, it was nothing of the sort; it was a disaster.
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Despite being raised as a girl, Joan never felt happy. At 12, she was given oestrogen therapy to complete the conversion to a woman. She grew breasts, but was never accepted by other girls, nor felt comfortable as a woman.
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At 14, she rebelled, confessing to her doctor: "I suspected I was a boy since the second grade." She was eventually given a mastectomy to remove the breasts and was given male hormones. At the age of 25, now John once more, he married a woman who already had children.
Dr Diamond says that the case history has implications for any child born with ambiguous sexuality. "Keep your knife away," he says. "Let the kids make a decision when they get older."
Michael Bailey, a psychologist at Northwestern University, Illinois, told Science Now, a daily science news service run by Science magazine, that the case was heralded by many as the pinnacle of proof that psycho-social factors could override biological factors in determining gender.
Textbooks continued to claim that Joan made a successful adjustment, in spite of contradictory evidence. Dr Diamond's report, says Dr Bailey, "suggests that, if anything, how you're reared matters little".
(Text extract from The Times, March 15 1997, by Nigel Hawkes. Pictures captured from a BBC TV programme "The boy who was turned into a girl", broadcast in December 2000)
We have seen that early exposure to testosterone affects the external genitalia and adult behaviour, but does it also change the brain? This is an important question. There is evidence that the brains of male and female rodents are structurally different, and that this sexual dimorphism is caused by exposure to androgen during a critical period of development.
An area of the hypothalamus at the base of the brain called the sexually dimorphic nucleus of the preoptic area (SDN-POA) is much larger in male rats than in females. These diagrams show the location of this sexual dimorphism. You can load an animation that explains the relationship between the saggital and coronal views of the brain in a separate browser window.
Abbreviations:
This animation shows you the location of the SDN and POA within the brain Use arrow / slider to rotate brain
There are four interstitial nuclei of the anterior hypothalamus (INAH) in the human brain that may be homologues (similar in structure and evolutionary origin) of the rat's sexually dimorphic nuclei (SDN).
This diagram shows a coronal section through the human hypothalamus at the level of the optic chiasm (OC). The four cell groups (INAH1, 2, 3 and 4) studied by Le Vay, (Science, Vol. 253, page 1034, 30th August 1991) are indicated by the corresponding numbers.
Le Vay (1991) reported that:
However it is quite difficult to interpret these results:
In the 23 October, 1997 issue of Nature, Dr Marc Breedlove of the University
of California, Berkeley provided an insight into these important questions.
"Breedlove studied male rats that copulated freely with constantly receptive females, and compared the structures of certain nerve tracts in their spinal cords with those of male rats caged with unreceptive females, and which therefore did not have the opportunity for intercourse. The nerve tracts studied by Dr Breedlove are known to be influenced by sexual factors, notably the presence of the male sex hormone testosterone. The result was clear -- sexual activity has an effect on the structure of the nervous system. The relevant nerve tracts were smaller in males that were free to copulate than in those that remained celibate. "
A neuroendocrine component, the positive estrogen feedback effect, thought
to be related to sexual orientation and, indirectly, to sexual differentiation,
was evaluated in healthy, non-institutionalized research volunteers.
Men and women with a lifelong heterosexual orientation and men with a
lifelong homosexual orientation were administered an estrogen preparation
known to enhance the concentration of luteinizing hormone in women but
not in men.
The secretory pattern of luteinizing hormone in the homosexuals in response
to estrogen was intermediate between that of the heterosexual men and that
of the women.
The diagram shows changes in LH in response to a single injection of Premarin.
From: Gladue et al, Science, 225, 1496-1499, 1984.
The interpretation of these results have been challenged and more recent
studies have failed to replicate the effect (Bem, 1996).
.. 43% of Americans believe that 'young homosexuals became that way because
of older homosexuals'
In an interview with Science in 1992 Bailey stated:
'No one has ever found a postnatal social environmental influence for homosexual orientation - and they have looked plenty'Changes in the psychiatric status of homosexuality
Until the early 1970's the study of homosexuality remained mostly in the domains of psychiatry. Different theories about the origins of homosexuality were advanced. Most of the theories associated homosexuality with psychopathology, caused by faulty upbringing, which included a domineering mother, a detached father or both. Inaccurate as this assumption was, it was not surprising because psychiatrists obtained their data only from people in therapy who had mental or emotional problems. In 1972 & 73 the American Psychiatric Assoc. deleted homosexuality as a disease from their diagnostic handbooks. The term "sexual preference" was introduced in the 1970's to correct the earlier concept that homosexuality was a disease or deviation. After 1982, as more scientists found evidence that homosexuality & heterosexuality may not be a matter of free choice, the term "sexual orientation" emerged & is commonly used today.
They found that the concordance rate of homosexuality for
Point to ponder: If homosexuality is due to a person's genetic make-up, how could the gene survive? Surely it would have disappeared due to homosexuals fathering less children?
Abstract: "A developmental theory of erotic/romantic attraction is presented that provides the same basic account for opposite-sex and same-sex desire in both men and women. It proposes that biological variables, such as genes, prenatal hormones, and brain neuroanatomy, do not code for sexual orientation per se but for childhood temperaments that influence a child's preferences for sex-typical or sex-atypical activities and peers. These preferences lead children to feel different from opposite- or same-sex peers--to perceive them as dissimilar, unfamiliar, and exotic. This, in turn, produces heightened nonspecific autonomic arousal that subsequently gets eroticized to that same class of dissimilar peers: Exotic becomes erotic. Specific mechanisms for effecting this transformation are proposed. The theory claims to accommodate both the empirical evidence of the biological essentialists and the cultural relativism of the social constructionists."
If homosexuality is due to a person's genetic make-up, how could the gene survive? Surely it would have disappeared due to homosexuals fathering less children?
"...natural selection should favor heterosexuality as it facilitates reproduction and the propagation of genes. .... what has maintained homosexuality in a small but consistent percentage of the human population?" (Muscarella et al. 2001)
Muscarella et al. (2001) review several evolutionary theories of homosexuality:
It strikes me that Rahman and Wilson's theory predicts that
At the risk of pointing out the blindingly obvious it is worth bearing in mind that homosexuals are perfectly able to have children.
Read Francis (2000) "Is Gender a social construct or a biological imperative?". Paper presented at the Seventh Australian Institute of Family Studies Conference Family futures: issues in research and policy: Sydney 24 - 26 July 2000. Available online
Francis argues that the term 'gender' has been politicized as part of the 'gender agenda' of contemporary feminism. She writes about her experiences in confronting these issues 'in the real world'. What is your position on the following issues/questions that she encountered:
References and recommended reading that expands on points covered in lecture: