Biological Sex and Sex Differentiation
(Moon Duchin)
First of all, an important question: why study biological sex
qua biology? My take on this is that while it is relatively
easy to believe that gender is culturally influenced,
socially constructed, or even purely performed, on the other hand
biological sex is often considered to confer baseline naturality
to the difference between males and females. Investigating
biology can shake up what naively seems to be a very real binary,
ultimately denaturalizing even this most basic human
dichotomy.
I. What are Male and Female?
The assignment of a male and female sex is only biologically
meaningful in sexually reproducing species where organisms produce
two different characteristic gametes (germ cells or sex cells made
through meiosis, these are
haploid, meaning they only possess half of the genetic complement).
In such species, the female is the organism which produces
the larger sex cell, while the male's is smaller
This means that for species which don't reproduce by combining gametes, or
those for which the gametes are mainly identical (isogamous species), male
and female are not defined. In some sense, then, women are biologically
constituted by association with that part of the species which produces
eggs, many times the size of sperm.
II. Animal Sex and Cultural Baggage
Because of the larger size of the female gamete, it is in general
less mobile than its male counterpart. This often, but not always,
corresponds to a bigger female role in gestation. This sometimes
leads to a more active female role in early child-rearing.
Mammals, male and female, have sexually sensitive tissue which
typically develops into
either an imperforate (no holes) clitoris,
or into a larger organ, the penis, which carries the urethra in males.
Two-Sex Species
- SPOTTED HYENAS. In this species, male and female have
genitals which are externally indistinguishable. They have an
important social role: hyenas recognize one another by sniffing
penises. Both are erectile. However, the female penis is highly
elastic, and both sex and birthing occur through the penis
(rather painfully for the female). Hyenas are also one of the few
species of canids which, in the human biological literature, are
considered to be female-dominant, a fact which many commentators
have linked to the presence of female penises.
(Stephen Jay
Gould on hyenas)
- REEF FISH. Most species of reef fish, and several others,
are capable of one or several changes of sex in their lifespans, both
protogynous (male-->female) and protoandrous (female-->male). Though
the examples are very diverse, there is one species that has gotten
disproportionately much attention: the Cleaner fish
(Labroides dimidiatus) travels in groups which appear to have
a single male at a time, which fertilizes eggs for all the females.
When the male dies, a female from the group changes sex and assumes
the male role. The typical term used by the fish biologists for
their living group is a "harem," and the male is presumed to hold
"complete dominance" over the females. In fact, in an influential
paper in the 1970s, D.R. Robertson opined that, "The ultimate ambition
of female Cleaner fish is to become male."
(fish
references)
- SEAHORSES. The male becomes pregnant and carries the
young to term. The female has no role in gestation.
"Before mating, the male seahorse changes his coloration and dances around
the female every morning for three
days (known as the "morning greeting"). On the third day, the male
twists his body to signal that his pouch is
empty, and with slow movements the female moves her head up and down in
a signal of approval if she is willing to
mate. Then the two dance belly-to-belly as the female transfers as many
as 1000 eggs to the pouch of the male.
The male fertilizes them inside his body and carries them for a
gestation period of two to three weeks. Each larvae
has its own tissue pocket and gets nutrients and oxygen from the male
bloodstream. The embryos' development is
regulated by the reproduction hormone prolactin (also found in female
mammals). At the end of the two- to
three-week period, he goes into a series of contractions and gives
birth to tiny, fully-developed juvenile seahorses
that are exact scale replicas of adult seahorses."
(reference)
- APES. There are four non-human species of ape: chimpanzee,
orangutan, bonobo, and gorilla (gibbons are sometimes included as well).
As these hominid primates are the closest evolutionary relatives of
humans, much has been made of their sexual behavior.
Gorillas and orangutans display extreme physical dimorphism, with males up
to twice the size of females. There are a few notable features of ape
sexuality which bear mention here. First, it is well-documented that
rape, or observably forcible sex, is common among orangutans. In fact, it
most frequently is carried out by so-called arrested males, young
males in whom puberty is deferred, sometimes for decades. It seems that
orangutans have some control over the hormonal onset of puberty, for
arrested males are frequent when dominant adult males exist in a social
group. Second, bonobos carry out many sexual activites that are
distinctly non-procreative, including oral sex, homosexual activity, and
face-to-face sex (the latter is very rare among non-human animals).
Bonobo
sex
Wholesale Projections of Sex
- E. COLI. With E. coli and in other bacteria, the F+ plasmid and F-
plasmid are identified by whether they are donors or recipients of genetic
information; on this basis alone, they are called "male" and "female"
respectively, as documented by Bonnie Spanier.
- ELECTRONICS. Those connections with appendages are called "male";
those with holes, "female."
III. Human Sexual Differentiation
Through six weeks, the human fetus is undifferentiated with
respect to sex ("sexually indifferent").
It has two sets of tissue that may or may not become activated,
the Mullerian ducts (which have the potential to become female
internal organs-- uterus, fallopian tubes, etc)
and the Wolffian ducts (which may become male
internal organs-- seminal vesicles, vas deferens, epididymis)
Between the sixth and the eighth week, the fetal body starts
to produce mass quantities of many hormones. [It's
important to note that a hormone, by definition, is any chemical, organic
or synthetic, which travels in body fluid, usually the bloodstream,
and regulates cellular physiology-- this is very broad! The most
famous hormones are only a few of a dizzying array that has
so far been identified.]
The egg carries an X chromosome, the sperm either an X or a Y.
Thus, typically, fertilized eggs have either XX (female) or
XY (male) as a karyotype (sexual genotype). In standard
XY development, at the 6-week stage, the Y begins to express:
testosterone is secreted along with MIS (Mullerian Inhibiting
Substance). There are many related structures and compounds:
SRY is the name of the gene that triggers the production of
H-Y antigen, which has a role in testicular development;
DHT (dihydrotestosterone) is the specific testosterone derivative
that governs development of external genitals in males.
What has been noted by feminist biologists at least since the
1980s is the total lack of study of the female chemical pathway.
Estrogen and progesterone are present in fetal
development as early as testosterone, but are not considered to
have an active role in morphological development. Note that
all three are extremely
structurally similar
members of the
cholesterol family, and that both males and females typically
produce all three in non-negligible quantities.
In utero, that is, in the womb, the fetus is exposed to
a rich soup of hormones, and in most cases the dimorphism
of male/female development is approximated fairly closely.
The second major round of hormones happens on time-release some
years later: puberty. At this time, people are exposed to
a blitz of hormones that induces rapid further sexual development,
along with secondary sex characteristics like body hair,
voice change, breast growth, and menarche (beginning of menstruation).
IV. Intersexuality
Let me emphasize that discussants of intersexuality have the
responsibility of retaining focus on personhood in discussions of
intersex people; speaking of intersex realities only in the
language of
conditions or disorders is disturbingly dehumanizing.
Furthermore, it is not so obvious how to
separate "them" from "us"-- significant departure from sex norms is
not only common, but is often undetected.
Because the chemical pathways of sexual differentiation are
so intricate, there are many developmental turns possible within the
standard XX/XY karyotypes. Here is a short collection of
biological possibilities.
- AIS (Androgen Insensitivity Syndrome)-- here, your
genotype is XY and your hormonal balance is typically male.
However, there are no cell receptors present which recognize
and express androgens (testosterone, DHT). The MIS, however,
is expressed, so the Mullerian ducts degenerate and the Wolffian
ducts develop: this means testicles are present, but undescended.
Externally, though, your genitals are female in appearance. You
never menstruate. The upper third of your vagina is not present,
and there is a possible range from the presence of the lower
two-thirds to merely a "dimple" (vaginal hypoplasia).
Particularly if a vaginal canal of some length is present,
you can go through your life unaware of this
condition, living as a woman. This was the case of Maria Patino,
a Spanish hurdler who was disqualified from international competition in
1988 after tests revealed her to be XY. (The testers advised her to fake
an injury and withdraw; she refused, and after the results were published
she lost not only the right to represent Spain but also her university
scholarship and her boyfriend.)
- Partial AIS conditions can result in testosterone being
produced but not fully expressed.
- 5-ARD (5-alpha-reductase Deficiency; also "Penis-at-Twelve")--
a certain enzyme is responsible for the transformation of testosterone
into DHT, which is the mechanism for fetal development of male external
genitals. Without DHT, then, you are born with external
genital anatomy ranging from typically female appearance to somewhat
ambiguous. However, since DHT is not the only mechanism for the
physiological effects of male puberty, you undergo "virilization" at the
onset of puberty, including in some cases the descension of testicles and
the growth to penis size of an erectile phallus. Some 5-ARD individuals,
after having been raised as girls, are subsequently considered men and go
on to father children. 5-ARD is heritable and is substantially more
common in certain gene pools, especially in the Dominican Republic (where
people whose sex is seen to shift at puberty are called
guevedoces, or penis-at-twelve), but also
in New Zealand and Turkey.
- DHT Deficiency-- similar effects to 5-ARD.
- CAH (Congenital Adrenal Hyperplasia)-- here, your genotype is XX, and
your initial sex hormone balance is typically female. (Actually, CAH can
occur in XY individuals as well, but there it does not cause an intersex
phenotype.) However, the adrenal gland does not produce cortisol (a
non-sex-related hormone) but instead creates more than usual amounts of
the other hormones it controls, including androgens. Thus there is often
partial
masculinization
of the genitals, including a large clitoris and
partial closure of the urogenital swellings, so that the labia are
incompletely fused into a scrotum. Cortisol is necessary to survival, so
in the most extreme cases CAH must be medicated daily. Furthermore,
operations are still routinely performed on CAH infants to excise or cut
down the "oversized" clitoris.
- AGS (Adrenogenital Syndrome)-- another name for CAH.
- Vaginal Agenesis (related to Mayer-Rokitansky-Kuster-Hauser
Syndrome)-- here, an XX baby is born without, or with a very short,
vaginal canal. Your uterus may be absent, or unusually small, as well.
This condition is still routinely
treated with the insistence that teen girls should "create" vaginas
through long and painful sessions with vaginal dilators in order to have
normative sexual function.
V. Karyotypes
Note the frequency figures are much debated; these come from mainstream
medical texts and they may be off by a factor of two, since they are
reported as, eg, "1 in 850 live male births," which I find
ambiguous given the context.
- Mosaicism-- two or more populations of cells in the same individual.
That is, not all of your body's cells have the same karyotype as each
other, usually caused by a change which occurs in an early stage of
mitosis (the repeated splitting of the zygote into more and more cells).
For instance, biologists now work under a modification of Mary Lyon's
hypothesis which holds that both X chromosomes of a female are not
simultaneously expressed-- either the paternal or the maternal X is
primarily active, while the other is suppressed to some extent. Since
this designation occurs around the 16-cell stage of mitosis, which X is
active varies among different cellular populations (say 6 chose the
paternal X and 10 chose the maternal X). In this sense, every normal
female exhibits a form of mosaicism.
- XX/XY-- the expected female and male karyotypes. Frequency unclear;
see rest of this section.
- XO (Turner's Syndrome: 1 in 3000)-- this involves monosomy of
the X chromosome; either the second sex chromosome is entirely absent, or
it is
structurally impaired from being expressed. You are typically
considered female. Turner's frequently manifests
in mosaic form, so that some cells are XO and others are of a different
type (this has been documented as occurring XO/XX, XO/XY, XO/XXX, and in
other configurations). Depending on the proportion of body cells with XO
type, the phenotype associated to Turner's Syndrome may range from
presence of readily detectable features to almost no difference from the
norm. In the most noticable cases, you may manifest some or all of these
associated features: short stature, low hairline, webbed neck, amenorrhea
(no menstruation), and no pubertal development of secondary sex
characteristics. (In fact, some degree of Turner's syndrome is believed
to be involved in as many of a third of cases of amenorrhea.)
- XXY (Klinefelter's Syndrome: 1 in 850)--
XXY is the most common karyotype, but Klinefelter's encompasses any
karyotype with two or more X chromosomes and one or more Y, possibly in
mosaic form with other types. You are phenotypically male; at puberty,
the sex development produces unusually small testes and often a small
penis. Klinefelter's is cited as the most common source of male
infertility.
Other physical features may include: elongated legs and lower body, low
IQ (but rarely retardation), lack of male secondary sex characteristics,
and some degree of breast development.
- XYY (1 in 1000)--
here, there is one X chromosome and there may be two or more Ys.
In the 1960s, police apprehended serial killer and sexual predator Richard
Speck. In his defense trial for the murder of eight nursing students, he
claimed that he had XYY chromosomes, which predisposed him to his
behavior. There followed a flood of research, early versions of which
claimed that these chromosomal conditions predispose men to low IQ,
sociopathic behavior, and heightened aggressiveness via
heightened testosterone. It is currently
considered that all of this research is inconclusive (much of it occurred
through testing on prison populations with questionable methodology), and
in fact it turned out that Speck himself was not XYY to begin with, but
garden-variety XY.
- Multi-X (1 in 1200)-- though relatively frequent, Multi-X appears to
have very little documentation (much less, for instance, than the rarer
Turner's syndrome).
As one medical text says, "Most of these
women are entirely normal. ...[T]here is an increased tendency to mental
retardation in proportion to the number of extra X chromosomes."
This seems to me to need further analysis.
VI. Cultural Sex Regulation
one potent example: sex testing for female athletes in the
Olympics
1966: Olympics begin "nude parade"
1968: gene tests
1996: only 4 sports still test (skiing, volleyball, weightlifting,
basketball)
1999: sex testing abandoned "unless high degree of suspicion"
At the Atlanta Olympics, the tests revealed eight women (of 3387 tested)
who had androgen insensitivity or 5-alpha reductase deficiency.