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Path: news.eternal-september.org!eternal-september.org!feeder3.eternal-september.org!nntp-feed.chiark.greenend.org.uk!ewrotcd!news.eyrie.org!beagle.ediacara.org!.POSTED.beagle.ediacara.org!not-for-mail From: MarkE <me22over7@gmail.com> Newsgroups: talk.origins Subject: =?UTF-8?Q?Re=3A_Observe_the_trend=2E_It=E2=80=99s_happening=2E_Give?= =?UTF-8?Q?_it_time=2E?= Date: Sun, 16 Mar 2025 22:26:34 +1100 Organization: A noiseless patient Spider Lines: 288 Sender: to%beagle.ediacara.org Approved: moderator@beagle.ediacara.org Message-ID: <vr6chf$1men7$1@dont-email.me> References: <vq8k3n$29ai1$1@dont-email.me> <vqar6h$2lnbh$1@dont-email.me> <vqehpj$3g1ui$1@dont-email.me> <vqghcq$41r$1@dont-email.me> <vqqdji$272c0$1@dont-email.me> <vquerg$375li$1@dont-email.me> <vqulv1$38q4g$1@dont-email.me> <vr0cvm$lk5d$1@dont-email.me> <vr508u$fu9i$1@dont-email.me> MIME-Version: 1.0 Content-Type: text/plain; charset=UTF-8; format=flowed Content-Transfer-Encoding: 8bit Injection-Info: beagle.ediacara.org; posting-host="beagle.ediacara.org:3.132.105.89"; logging-data="48486"; mail-complaints-to="usenet@beagle.ediacara.org" User-Agent: Mozilla Thunderbird To: talk-origins@moderators.isc.org Cancel-Lock: sha1:Tl6ygpPiSHXI3Fb6NzKMs8foy6E= Return-Path: <news@eternal-september.org> X-Original-To: talk-origins@ediacara.org Delivered-To: talk-origins@ediacara.org id F223B22978C; Sun, 16 Mar 2025 07:26:52 -0400 (EDT) by beagle.ediacara.org (Postfix) with ESMTPS id A99D7229783 for <talk-origins@ediacara.org>; Sun, 16 Mar 2025 07:26:50 -0400 (EDT) id 78F301C0934; Sun, 16 Mar 2025 11:26:43 +0000 (UTC) Delivered-To: talk-origins@moderators.isc.org by newsfeed.bofh.team (Postfix) with ESMTPS id 67C0F1C0390 for <talk-origins@moderators.isc.org>; Sun, 16 Mar 2025 11:26:43 +0000 (UTC) (using TLSv1.3 with cipher TLS_AES_256_GCM_SHA384 (256/256 bits) key-exchange X25519 server-signature ECDSA (P-256)) (No client certificate requested) by smtp.eternal-september.org (Postfix) with ESMTPS id 4ACCD622B6 for <talk-origins@moderators.isc.org>; Sun, 16 Mar 2025 11:26:41 +0000 (UTC) Authentication-Results: name/4ACCD622B6; dmarc=fail (p=none dis=none) header.from=gmail.com id 06E5BDC01CA; Sun, 16 Mar 2025 12:26:40 +0100 (CET) X-Injection-Date: Sun, 16 Mar 2025 12:26:40 +0100 (CET) X-Auth-Sender: U2FsdGVkX1/LReFb3VYgtFKKcEevZdqYpIaaPAiXm3g= In-Reply-To: <vr508u$fu9i$1@dont-email.me> Content-Language: en-US DKIM_ADSP_CUSTOM_MED,HEADER_FROM_DIFFERENT_DOMAINS,NML_ADSP_CUSTOM_MED, RCVD_IN_DNSWL_BLOCKED,RCVD_IN_ZEN_BLOCKED_OPENDNS,SPF_HELO_NONE, SPF_PASS,URIBL_BLOCKED,URIBL_DBL_BLOCKED_OPENDNS, URIBL_ZEN_BLOCKED_OPENDNS,USER_IN_WELCOMELIST,USER_IN_WHITELIST autolearn=ham autolearn_force=no version=3.4.6 smtp.eternal-september.org On 16/03/2025 9:51 am, Ernest Major wrote: > On 14/03/2025 04:57, MarkE wrote: >> On 14/03/2025 12:18 am, Ernest Major wrote: >>> On 13/03/2025 11:17, MarkE wrote: >>>> On 12/03/2025 9:31 am, Ernest Major wrote: >>>>> On 08/03/2025 04:34, MarkE wrote: >>>>>> On 7/03/2025 9:29 pm, Ernest Major wrote: >>>>>>> On 06/03/2025 00:45, MarkE wrote: >>>>>>>> On 5/03/2025 3:31 pm, MarkE wrote: >>>>>>>>> Is there a limit to capability of natural selection to refine, >>>>>>>>> adapt and create the “appearance of design”? Yes: the mechanism >>>>>>>>> itself of “differential reproductive success” has intrinsic >>>>>>>>> limitations, whatever it may be able to achieve, and this is >>>>>>>>> further constrained by finite time and population sizes. >>>>>>>>> >>>>>>>> >>>>>>>> <snip for focus> >>>>>>>> >>>>>>>> Martin, let's stay on topic. Would you agree that there are >>>>>>>> limits to NS as described, which lead to an upper limit to >>>>>>>> functional complexity in living things? >>>>>>>> >>>>>>>> How these limits might be determined is a separate issue, but >>>>>>>> the first step is establishing this premise. >>>>>>>> >>>>>>> >>>>>>> First, natural selection is not the only evolutionary process. >>>>>>> Even if one evolutionary process is not capable of achieving >>>>>>> something that doesn't mean that evolutionary processes in toto >>>>>>> are not capable of achieving that. >>>>>> >>>>>> Natural selection is the *only* naturalistic means capable of >>>>>> increasing functional complexity >>>>> >>>>> Creationists have been known to argue that natural selection >>>>> doesn't create anything; it merely selects what's already present. >>>>> As an argument against evolution that's worthless; but as an >>>>> observation it's true enough. Each step in functionality complexity >>>>> originates from mutation, or recombination, or gene flow, and is >>>>> subsequently fixed or not by natural selection or genetic drift. >>>>> >>>>> For example Ron Okimoto (I think) recently mentioned that one >>>>> flagellar gene is a truncated version of another, and results in >>>>> the assembly of a tapered flagellum rather than cylindrical one. I >>>>> can imagine that the tapered flagellum is advantageous, and was >>>>> fixed by selection. It might be that the gene was duplicated and >>>>> fixed by drift before a truncation mutation occurred, but as >>>>> selection against excess DNA is effective in bacteria I suspect >>>>> that it originated as a partial duplication of the gene, which was >>>>> then selected. But note that the initial increase in complexity was >>>>> caused by the mutation. Natural selection fixes this in a >>>>> population, and as you have mentioned acts as a ratchet allowing >>>>> changes to accumulate. >>>>> >>>>> But you are assuming increases in functional complexity are >>>>> adaptive. They could be neutral or slightly deleterious and fixed >>>>> by genetic drift. I don't accept without question your >>>>> panadaptationist/ panfunctionalist premise. >>>>> >>>>> Passing over the problems with defining an objective criterion for >>>>> irreducibly complex systems, there are at least three classes of >>>>> evolutionary paths to this. I think that coadaptation is the >>>>> predominant one. This goes from non-interaction to facultative >>>>> interaction to obligate interaction. Both steps could be fixed by >>>>> either natural selection or genetic drift. >>>>> >>>>>> and genetic information. >>>>> >>>>> Increases in functional complexity and genetic information are not >>>>> the same thing. If you use a Shannon or Kolmgorov measure natural >>>>> selection tends to reduce, not increase, information in a gene pool. >>>>>> >>>>>> All other factors have only a shuffling/randomising effect. In >>>>>> every case, NS is required to pick from the many resulting >>>>>> permutations the rare chance improvements. >>>>>> >>>>>> Without the action of NS, all biological systems are degrading >>>>>> over time. >>>>>> >>>>>>> >>>>>>> Second, you've changed the question. Evolutionary processes have >>>>>>> limitations, but those limitations need not be on the degree of >>>>>>> functional complexity achievable. Evolution cannot produce living >>>>>>> organisms that can't exist in the universe. (You could quibble >>>>>>> about lethal mutations, recessives, etc., but I hope you can >>>>>>> perceive the intent of my phrasing; for example, I very much >>>>>>> doubt that evolution could result in an organism with a volume >>>>>>> measured in cubic light years.) >>>>>>> >>>>>>> Applying this to functional complexity, physical limits on how >>>>>>> big an organism can be, and how small details can be, do pose a >>>>>>> limit on how much functional complexity can be packed into an >>>>>>> organism. But such a limit doesn't help you - humans are clearly >>>>>>> capable of existing in this universe, so aren't precluded by that >>>>>>> limit. You need a process limitation, not a physical limitation; >>>>>>> I don't find it obvious that there is a process limitation that >>>>>>> applies here. >>>>>>> >>>>>>> You say that the first step is establishing the premise. That is >>>>>>> your job. >>>>>>> >>>>>>> That there are things that evolution cannot achieve (a classic >>>>>>> example is the wheel, though even that is not unimaginable) >>>>>>> doesn't not mean that evolution cannot achieve things that >>>>>>> already exist; one of the reasons that ID is not science is it's >>>>>>> lack of interest in accounting for the voluminous evidence that >>>>>>> evolution has achieved the current biosphere. >>>>>>> >>>>>> >>>>>> The limits of NS are not simply due to physically possible >>>>>> organisms. It's much tighter constraint. The mechanism of >>>>>> "differential reproductive success" is a blunt instrument, rightly >>>>>> described as explaining the survival but not arrival of the fittest. >>>>>> >>>>>> To elaborate my hypotheses (not proofs): >>>>>> >>>>>> 1. NS, along with any other naturalistic mechanisms, do not have >>>>>> the logical capacity to fully traverse the solution space, >>>>>> regardless of time available. Some (many) areas of the fitness >>>>>> landscape will be islands, local maxima, inaccessible via >>>>>> gradualistic pathways (e.g. monotonically increasing fitness >>>>>> functions). These are however accessible to intelligent design. >>>>> >>>>> You are moving the target again. It is not legitimate to take the >>>>> probably truism that evolution cannot reach all targets, and use >>>>> that to argue that are limits to the degree of complexity that >>>>> evolution can generate. >>>> >>>> I'm not claiming a limit the degree of complexity that evolution can >>>> generate, but rather the extent of of the solution space. >>> >>> "Would you agree that there are limits to NS as described, which lead >>> to an upper limit to functional complexity in living things?" - >>> MarkE, 5th March 2025. (Quoted by MarkE on the 13th March 2025 - see >>> above.) >>> >> >> To recap different contributing factors to an upper limit in >> functional complexity in living things in relation to natural selection: > > You were being invited to address your vacillation about whether you > claim that there is an upper limit to the amount of functional > complexity that evolution can generate. >> >> 1. Fitness landscape >> >> If the fitness landscape has unreachable islands (local maxima >> sparsely distributed in a plain), then if some of these represent ========== REMAINDER OF ARTICLE TRUNCATED ==========