Taking a new tack with the common descent/common design theme, I’d like to sneak up on it. As Sal Cordova likes to do, I offer a hypothesis for critique. Here’s an old phyogenetic analysis of mine. Does it show common descent? If not, what’s wrong with it?
This one is about crocodiles. Are crocodiles all the same kind? How do you know? If they aren’t how many kinds are there within the group and how do you know? If they are, are they a whole kind or just part of a larger kind? And if the latter, what is the larger kind?
Mung,
Another way to state my problem with you is that almost every comment you make is an attempt at a “gotcha”, but it generally involves you misinterpreting what someone else has said.
Mung,
Don’t forget that feathers also evolved for sexual advances… you see evolution was working on making dinosaurs to fly but forgot to curb their appetites… since they got too fat, evolution changed its mind and made them use feathers to attract potential mates… you see how clever evolution is… which obviously evolution predicts…
Thanks for the reminder. But Glen didn’t actually say that, while he did say the other two I mentioned.
Well, yes, I engage in “gotcha” but so does your side. Perhaps it’s due to my own misunderstanding. There’s plenty of hypocrisy to go around for everyone. It’s not in short supply. 🙂
And we do have a recent example of you doing the same thing. Remember when you “corrected” me about what it is that defines a clade? Later on Rumraket made essentially the same claim that I made but you declined to “correct” him.
Maybe both of us can do better.
When I was researching Noah’s Ark, I came across an interesting fact: the length to width to height ratio is 30 to 5 to 3. I found that this ratio is commonly used in large ships that are designed not for speed. The ark was designed to float and not for speed…
How could bible writer few thousand years ago know what the ideal ratio of a huge wooden box would be for floating if that was experimentally proven less than 100 years ago and still remains as an engineering ship building formula for big slow ships…
The paper doesn’t compare the morphological and molecular characters evolution.
It compares the characters of both and presumes evolution has been going on.
Where is your evolution evidence thats being compared??
I read carefully your post but big word combinations don’t make a point that everything in this is simple grouping of traits. Atomic or bodypland!
Thats it and no more.
why they score as they do is another issue.
The trees looking the same, not enough however to not overthrow a previous conclusion, would be this way from other options.
Like COMMON DESIGN.
Why not?
Evolutionists show thoughtful creationists they are not doing scientific investigation of the origins of biology WHEN they start off with boundaries for options for same origins.
COMMON DESIGN must be a option for likeness in traits/characters.
By the way. If morphology had a atomic score/code it should match genetics.
Changing the morph changes the genes and opposite.
for example i’m certain marsupials are just adjusted placentals.
yet they have genetic scores with marsupial scores being quite loud.
So this means the marsupial genes is just thrown on top after the morphing/gene change.
You misunderstand me, I was agreeing with Allan that there is no “definitive” case for common descent in the sense that definitive means proof.
J-Mac,
You asked a question, I answered.
Mung,
As is his own response thereto. Doesn’t really affect what I say though.
In his response to criticism he discusses the difference between model selection and more traditional approaches relating to null hypotheses. In the latter, you either reject or fail to reject the null, you don’t confirm the null. Proving non-relationship would be confirming the null, IMO.
In my response to you I was not thinking of Theobald, but of that kind of ‘null’ approach. I was thinking just in terms of species pairs. If a species (or simply a sequence) pair has no alignment beyond the expectation of two ‘random’ sequences, you haven’t proven their non-relationship, just failed to find any relationship.
Theobald is a little more subtle: it’s about treelike topology – not just species pairs, but the concordance of the overall pattern with the expectation of common descent – which, bizarrely, you still seem to think has no expectation: But it does: trees.
Of course you can. On common descent, a treelike topology is more probable than a ‘random’ arrangement, because common descent means that species pairs tracing back to a common ancestor will have that ancestor’s genes, albeit somewhat scrambled by subsequent mutation. This holds through additional bifurcations, building up from single nodes to trees. So, if you find a treelike topology in a set of character states – better yet if you find the same broad tree in another set – you have pretty strong evidence that common descent lies at the heart of it.
So we have
1) new (deleterious) alleles introduced by mutation.
and
2) radiation (branching evolution) of lineages from a few ancetral kinds
And now for the million dollar question. Are you ready?
How exactly will those mutations be distributed across the resulting lineages. Will that resemble a nested hierarchy perhaps?
So crocks are NOT lower organisms? What exactly do you mean with lower organisms? Are we talking scala naturae here?
Let me get this straight: Humans started out with a perfect polyconstrained genome (plus all the other -omes stacked on top). Still, we were able to tolerate numerous mutations that created, among other things, pseudogenes without suffering severely debilitating effects. Right? And then because we have acrued a number of deleterious mutations, backmutations create beneficial alleles by restoring the original function.
Hence you concede that junk DNA exists (pseudogenes) and the possibility of beneficial alleles by random mutation. Did I understand that correctly?
One of the two uses was lucky, either the flying part or the insulation part, the other one was…. Was evolved for!
So, to summarize: there’s nothing wrong with the paper, and it either is or is not evidence for common descent of crocodylians, depending on which creationist is talking and, apparently, the relative humidity at the time, because Jesus. I had hoped for more.
This one is about crocodiles. Are crocodiles all the same kind? How do you know? If they aren’t how many kinds are there within the group and how do you know? If they are, are they a whole kind or just part of a larger kind? And if the latter, what is the larger kind?
The real beauty of Hirschman’s paper that it fits any imaginable scenario, including the option that crocks didn’t go to the Ark and just floated in the water… No matter what idea one has about crocks’ origins, harshman’s phylogenic analysis fits it…
Who can argue with this piece of experimental science?
Except that no wooden ship has ever been built to those dimensions. Johan’s Ark in the Netherlands (which is a full-scale replica) needs the support of 21 steel barges to keep it afloat. Even Huibers’ half-scale replica is barely seaworthy and cannot stand waves of any significant height.
And length-to-width and length-to-draft ratios of transport ships vary widely across the industry depending upon application. I’m sure you can find a subset which adhere roughly to the ratio that you have stated, but that hardly constitutes a magic number.
A bottleneck suggesting a foundry population for domesticated animals less than 10,000 years ago doesn’t sound particularly far-fetched to me. Archaeological evidence puts the Neolithic Revolution at the end of the Holocene around 12,500 years ago when agriculture and widespread animal domestication appear to have been invented.
Good luck coming up with evidence for a similar bottleneck in wild animals though.