<obligatory-caveat-of-ignorance>

But I suppose it makes some sense to eliminate the concept of inheritance and 
focus on variation. Inheritance assumes a discreteness in traits that variation 
doesn't. And in this way, we might track the ontogeny (intra-generational 
variation) of units of selection similarly to tracking inter-generational 
variation.

But this would require a rigorous similarity measure. In "space", as 2 units 
evolve over time, we need some concept of how [dis]similar they become. In time, as a 
unit evolves, does it wander, or cycle, or [con|di]verge? It seems to me that *how* that 
similarity measure is constructed becomes the difference between kin vs group selection. 
Differences measured off organisms (blue eyes and hyena penises) would preference 
organisms as the unit. Differences measured off groups (altruism and religion) would 
preference groups. Only a mix of both organism and group differences could construct an 
agnostic similarity measure.

</obligatory-caveat-of-ignorance>

We had such a conversation last night in the context of adversarial exploration strategies. E.g. 
when 2 opponents in a game like, say, traditional boxing, trashtalk each other, that ad hominem 
serves the functional purpose of polarizing them and increasing their ability to find the corner 
cases in the space circumscribed by the boxing game. But as well-defined as that game is, there are 
still "parasitic" behaviors that identify some players as acting in bad faith. Those 
"parasitic" behaviors are thought (normatively) to NOT target a better collective 
understanding of the space circumscribed by the explicit rules. If we expand beyond the particular 
game to related games like wrestling and kick-boxing, or to define a broader game like MMA, we rely 
even more on our ability to identify, informally, bad faith actors. We could construct a similar 
story for fintech (e.g. 2008 crash), eusocial insects, or (I'm guessing) any other potential 
grouping. Unless we measure variables from across a large spectrum of granularity, we won't be able 
to tell what variation correlates with what potential unit of selection.

Even if group selection can be shown to be mathematically isomorphic to kin 
selection, and there's a theoretically sound but computationally infeasible way 
to model cross-grain evolution from either perspective, it'll still be 
*convenient* to model and explain it at higher levels ... in the same way that 
it's convenient to explain, say, Swing music without resorting to quantum 
mechanics.

And on that note, since I know we have a few Ψ enthusiasts here:

Psychedelics alter metaphysical beliefs
https://www.nature.com/articles/s41598-021-01209-2


On 1/4/22 15:42, thompnicks...@gmail.com wrote:
If memory serves methylation can prevent the expression of a gene for a 
generation or so because of some experience the gene endures, like being in  a 
male or a female, for instance.  Lamarckism, is the principle that animal can, 
by striving to achieve a goal, increase the likelihood that “factors” advancing 
those goals will appear in its offspring.  Both involve an effect upon what is 
inherited by experience, but I think their structure is quite different.  But 
it’s been a while.

n

Nick Thompson

thompnicks...@gmail.com <mailto:thompnicks...@gmail.com>

https://wordpress.clarku.edu/nthompson/ 
<https://wordpress.clarku.edu/nthompson/>

*From:* Friam <friam-boun...@redfish.com> *On Behalf Of *Marcus Daniels
*Sent:* Tuesday, January 4, 2022 5:29 PM
*To:* 'The Friday Morning Applied Complexity Coffee Group' <friam@redfish.com>
*Subject:* Re: [FRIAM] Group Selection Redux?

Isn't Lamarckism alive and well with the existence of DNA methylation?   
Finding a way to thread the needle to get altruism and so forth out of genetic 
inheritance seems rather academic?

------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------

*From:*Friam <friam-boun...@redfish.com <mailto:friam-boun...@redfish.com>> on behalf of 
thompnicks...@gmail.com <mailto:thompnicks...@gmail.com> <thompnicks...@gmail.com 
<mailto:thompnicks...@gmail.com>>
*Sent:* Tuesday, January 4, 2022 3:27 PM
*To:* 'The Friday Morning Applied Complexity Coffee Group' <friam@redfish.com 
<mailto:friam@redfish.com>>
*Subject:* Re: [FRIAM] Group Selection Redux?

J.

You don’t address the point that Wilsons trait-group selection mechanism is 
actually an INHERITANCE mechanism.  Is that because you don’ get it, or because 
you don’t like it and are being polite.

n

Nick Thompson

thompnicks...@gmail.com <mailto:thompnicks...@gmail.com>

https://wordpress.clarku.edu/nthompson/ 
<https://wordpress.clarku.edu/nthompson/>

*From:* Friam <friam-boun...@redfish.com <mailto:friam-boun...@redfish.com>> 
*On Behalf Of *Jochen Fromm
*Sent:* Tuesday, January 4, 2022 3:59 PM
*To:* The Friday Morning Applied Complexity Coffee Group <friam@redfish.com 
<mailto:friam@redfish.com>>
*Subject:* Re: [FRIAM] Group Selection Redux?

:-) D.S. Wilson is one of the few who is on the right path. What he gets right is that 
social groups can sometimes be treated as adaptive units whose organization cannot be 
reduced to individuals or individual interactions [1]. This is what he emphasizes in his 
articles about group selection and in his book "Darwin's Cathedral" [2].


The question is what is selected? In natural selection a genotype is selected 
if the phenotype has high fitness and lots of offspring. For individual animals 
it is clear. For groups we can argue that successful groups are selected if 
their phenotype has high fitness and attracts lots
of new members. This naturally leads to the question "what is the genotype and the 
phenotype for groups" ?

The phenotype is apparently the group character which is characterized by group 
traits as you mentioned. The group traits are in turn created by the common 
rules of the group, which can be commandments or norms or laws. The only thing 
that I miss in Wilson's work is that these rules are identified as what they 
are (as the genes that can create a group if they are expressed and applied 
regularly).

If we define and identify the genotype and the phenotype correctly, then we can 
really shift the metaphor of the selfish gene and the metaphor of natural 
selection to the group level, as the title of your paper says.

[1] David Sloan Wilson, Elliott Sober, "Reintroducing group selection to the human 
behavioral sciences". Behavioral and Brain Sciences 17 (4) (1994) 585–654


[2] David Sloan Wilson, "Darwin's Cathedral: Evolution, Religion, and the Nature of 
Society", University of Chicago Press, 2002

-J.

--
glen
Theorem 3. There exists a double master function.

.-- .- -. - / .- -.-. - .. --- -. ..--.. / -.-. --- -. .--- ..- --. .- - .
FRIAM Applied Complexity Group listserv
Zoom Fridays 9:30a-12p Mtn UTC-6  bit.ly/virtualfriam
un/subscribe http://redfish.com/mailman/listinfo/friam_redfish.com
FRIAM-COMIC http://friam-comic.blogspot.com/
archives:
5/2017 thru present https://redfish.com/pipermail/friam_redfish.com/
1/2003 thru 6/2021  http://friam.383.s1.nabble.com/

Reply via email to