On Fri, Nov 21, 2008 at 2:17 PM, Tony <[EMAIL PROTECTED]> wrote:
> but if none of those homosexual men had heterosexual sisters, then eventually
> it would die off.  your essay, although well written seems to assume a lot and
> not look at the instances like what i described above.
>

You are correct, an entirely homosexual population would certainly die
off (pending future technological advances). But the point I keep
trying to make isn't that homosexuality is evolutionarily the bees
knees (it is obviously not since it doesn't even seem to represent the
majority of the individuals in the human population) but rather that
it is a mistake to think that its an abomination of nature and that it
is selected against evolutionarily. Lots of traits can and do wander
around between a maximum frequency in the population (gets too
frequent and an alternate trait is favored) and minimum frequency (the
trait is favorable enough that it tends to not die out).

I'll give you a real world example: Sickle cell anemia. Its a classic
case studied in evolutionary biology. Sickle cell anemia is an
inherited genetic disorder that distorts your red blood cells in such
a way that they can't bind to oxygen molecules to transport them
through your blood stream. We've known for quite some time that
African American's have a much higher incidence of this disease than
people of caucasian descent. And you would think that this disease
would be strong selected against because it causes people to have low
amounts of energy, bleed easily and usually die younger.

So why would sickle cell anemia still be present in the population and
in particular, why would it be so much more prevalent in people of
African descent? Well, it turns out that if you have two copies of the
allele that causes sickle cell anemia, you end up with sickle cell
anemia. But if you only have one copy of the allele, it turns out that
you have a higher resistance to malaria. Malaria has been (and still
is) one of the biggest killers in sub-Saharan Africa.

Consider then two people who have one allele for the gene that
produces sickle cell anemia. They themselves don't have sickle cell
anemia. And they are more resistent to malaria than the people around
them with no copies of that allele. Lets say they have 4 kids. With
basic mendellian genetics we'd say that the odds are that one child
will have two copies of the allele and have sickle cell anemia, one
child will have no copies of the allele but also not have a higher
immunity to malaria and two children will have one copy of the allele
and have higher resistence to malaria and not have sickle cell anemia.

In that way, a trait that can be maladaptive in some cases (anemia)
but beneficial in others (malaria) ends up maintaining a non-zero
baseline frequency in the population. But if you look at people of
caucasian descent, they've been living outside the tropics long enough
that malaria hasn't been a problem for them for a long time and
consequently the downside of anemia risks have outweighed the benefits
of malaria resistance and consequently the allele has gone to a very
low frequency in that population.

Judah

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