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Old 04-29-2002, 06:39 AM   #321
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Quote:
Originally posted by Ed:

Ed: All of the [fossil skulls] that I said were human are well within the range for humans 700cc to 2200cc.
OC: Please provide references for such a wide human range. You didn’t just make it up, now did you?

It came from "Races, Types, and Ethnic Groups" by Stephen Molnar.
Ah, I thought it might. From <a href="http://www.talkorigins.org/faqs/homs/a_brains.html" target="_blank">here</a>:

Quote:
These figures also show how extraordinary the Turkana Boy is. As an adult, he would have been around 183 cm (6'0") tall, large even by modern standards. Modern men of that stature would be expected to have a larger than average brain size, but the Turkana Boy's estimated adult brain size of 910 cc is smaller than all but a fraction of 1% of modern humans of all sizes and both sexes. For comparison, 900 cc is a typical brain size for a modern child of 3 or 4 years weighing 15 kg (33 lbs).

Lubenow (1992) states that the lower limit of human cranial capacity is 700 cc, a much lower figure than anyone else. His source is Races, Types and Ethnic Groups by Stephen Molnar. Molnar says that "there are many persons with 700 to 800 cubic centimeters", but provides no source for this information, and none of his sources appear to do so either. In fact, one of his sources contradicts Molnar (and Lubenow). Tobias (1970) says that according to Dart, "apparently normal human beings have existed with brain-sizes in the 700's and 800's" (maybe Molnar's claim is a mis-statement of this), and that the smallest cranial capacity ever documented is 790 cc.

This strongly contradicts Molnar's claim that "many" modern humans have a cranial capacity below 800 cc, and Lubenow's derived claim that anything above 700 cc is a "normal" value. Instead, it appears from a variety of sources that values below 900 cc are very rare, and values below 800 cc virtually nonexistent.

Even if exceptional humans were found as low as 700 cc, it would still be implausible for Lubenow to claim that ER 1470, at 750-775 cc, is "well within the normal human range". (One might equally validly claim that an adult height of 122 cm (4'0") is well within the normal range on the grounds that some people are only 107 cm (3'6") tall.) Such cases, if they even occur, are obviously exceptionally rare, and the probability of finding a fossil human skull with such a small brain is essentially zero. It is far more probable that 1470 was a fairly typical member of its population. This is what we find: other habilis fossils, very similar to 1470, are even smaller, and well below Lubenow's lower limit of 700 cc.

Chimpanzees have a brain size between 300 and 500 cc, with an average of 400 cc. Gorillas have an average brain size of 500 cc, with large individuals going up to 700 cc, or even 752 cc in one reported (but unverifiable) instance. Hominids are best compared with the similar-sized chimpanzees than the much larger gorillas.

Lubenow states that "the crucial element is not brain size but brain organization. A large gorilla brain is no closer to the human condition than is a small gorilla brain". Lubenow's point is correct. If evolution is true, transitional creatures with brain sizes between 650 and 800 cc must have existed, but finding a skull with such a brain size does not prove that its owner was a transitional form. To be a convincing transitional form, a skull should not only have an intermediate brain size, but also an intermediate morphology.

This is exactly what is found in some H. habilis fossils. While there are no habiline fossils for which both brain and body size can be measured, it is fairly clear that they were smaller than humans, and many times smaller than male gorillas, the only apes with comparable brain sizes. Nor do H. habilis skulls have the crests and bone ridges found in large ape skulls. In addition, the insides of their skulls show many modern features (Tobias 1987). They are both larger and more modern, internally and externally, than the skull of any comparably sized ape.
Hmmm...

Quote:
No, they plainly do make a distinction between humans and apes. It is how they differentiate between Australopithicines and the Homo "species".
You do know that those are just the names the fossils are assigned to, don’t you? ‘Southern Ape’ is just the name, it doesn’t confer any greater ‘apeness’ on the fossils!

Why then the problems with whether Homo habilis is an ‘ape’ or a ‘human’?

Quote:
OC: You can provide references, of course [for the 90% cerebral-fluid-filled college lad’s head]?

Yes, see my post to lp above.
Thanks. I’d already checked that, see my post of 23/4.

Quote:
Ed: The main differences between mammals and reptiles occur in their soft tissue such as the heart and reproductive organs.
OC: Um, ear bones? Jaws? Differentiated dentition? Limb posture? Palate?

Some animals have very similar skeletal structures and yet are totally unrelated. I.e., marsupial and placental dogs. That is probably the case with some of these ancient mammals and reptiles.
Haha! You do know what a derived characteristic is, don’t you? So despite the jaw joints, differentiated teeth, palate and posture amongst other things, all of which are mammalian characters, these things are still reptiles?

(split since this seems too long to ba accepted... )
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Old 04-29-2002, 06:39 AM   #322
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Ed: Since this is not fossilized in the mammalike reptiles this connection is highly speculative.
OC: To you, because you want it to be. Everything we can tell from what we do have indicates transition between major groups.

Just because something is suggestive of a lineage doesnt necessarily mean there actually is one and see above about how skeletons can look very similar and yet be totally unrelated or ancestral.
Go learn some basic cladistics. Here is a good <a href="http://www.nhm.ukans.edu/cc.html" target="_blank">online cladistics textbook</a>.

Quote:
Ed: In addition, studies of the their skull endocasts show that their brains were typical of reptiles.
OC: Which Synapsids? References please.
All of them. "Evolution of the Brain and Intelligence" by H. Jerison.
Sorry, you’ll need to state what Jerison says, because according to André Wyss (‘Digging Up Fresh Clues About the Origin of Mammals’, Science, Vol 292, No 5521 (2001), p 1496-1497):

Quote:
The new fossil, Hadrocodium, is distinctive in numerous ways, perhaps the most striking of which is its exceedingly small size (its estimated body mass is about 2 g). Meticulous anatomical and phylogenetic analyses by Luo and colleagues reveal that Hadrocodium diverged before the appearance of the most recent common ancestor of monotremes and therians. So, strictly speaking, it is not a mammal, but is a member of the Mammaliaformes--a broader grouping comprising mammals and some of their closest fossil allies. However, as the nearest securely identified relative of mammals, Hadrocodium has proved uniquely valuable for documenting the sequence of morphological changes that led to the emergence of mammalian ancestors. If it were not for the synapsid fossil record, we would know only that myriad evolutionary novelties--such as three middle ear bones and a lower jaw composed of a single bone--appeared sometime before the divergence of monotremes and therians, and sometime after the divergence of mammals and their nearest living relatives, the reptiles. Instead, from analyses of Hadrocodium and many other fossils, we have a detailed understanding of the long sequence of changes that resulted in these unique structures.

Hadrocodium is firmly positioned as the nearest fossil relative of mammals, thereby clarifying which morphological features are ancestral for Mammalia. Besides three middle ear bones and a single jaw bone, Hadrocodium shares other evolutionarily unique features with mammals, such as an advanced configuration of the secondary palate and an elevated and anteriorly shifted craniomandibular (jaw) joint.

Another intriguing feature of Hadrocodium is its cranium, which is enormous compared to those of its contemporaries. Remarkably, mammaliaforms exhibit a huge range in cranium volume (relative to skull width). This wide variation evinces the plasticity of this feature among mammaliaforms and the considerable evolutionary convergence (or reversal) associated with cranial enlargement during mammaliaform evolution. This is by no means the only feature of mammaliaforms noted for its plasticity. In fact, mammaliaform features exhibiting convergence or reversal are almost as numerous as features considered to be evolutionarily more stable.
And Zhe-Xi Luo (‘A New Mammaliaform from the Early Jurassic and Evolution of Mammalian Characteristics’, Science Vol 292, No 5521 (2001), p 1535-1540) says:

Quote:
The second suite of derived features is related to the enlargement of the brain in Hadrocodium (Fig. 3). Its cranial vault is wider and more expanded in the alisphenoid and parietal region than those of all other nonmammalian mammaliaforms (7, 10, 14, 23) and all other Jurassic mammals (31-34) known to this date. The brain vault in the parietal region in Hadrocodium is comparable to those of the mammalian crown group (31-34), but wider than in nonmammaliaform cynodonts (24, 25), Sinoconodon (14), Morganucodon (10, 33), and Haldanodon (23) (Fig. 3). On the basis of the allometric scaling of a large sample of living and fossil mammals, the brain vault of Hadrocodium is larger than expected for the mammals of its comparable skull width (Fig. 5A) and far wider than in any other Triassic-Jurassic mammaliaforms. Our scaling analysis shows that the small size of Hadrocodium, in and by itself, is not sufficient to explain its large brain (Fig. 5A). Related to the expansion of the brain vault, the cerebellar portion of the brain cavity is expanded more posteriorly than the level of TMJ (Figs. 1A and 3D). The occipital (posterior) wall of the brain cavity is convex posteriorly beyond the lambdoidal crest (Fig. 1A), instead of concave or flat as in cynodonts, other mammaliaforms, and all Jurassic mammals known to this date (7, 10, 14, 23-27).
So please find what Jerison says, cos these folks don’t seem to regard these critters as all having typical reptile brains. [Edited to add: they don't mention reptile brains at all, which is rather odd if this is the case.]

That’ll do for no, more to follow...

TTFN, Oolon

[ April 30, 2002: Message edited by: Oolon Colluphid ]</p>
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Old 04-29-2002, 08:13 PM   #323
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Quote:
Originally posted by lpetrich:
<strong>
Ed:
As I demonstrated in the EOG thread a superintelligent hamster in your basement can be logically eliminated as creator of the universe.

lp: However, if that hamster is capable of reaching back in time and creating some initial quantum singuarlity or whatever, it could do the job.[/b]
How could he reach back in time if he didnt exist? You know we are talking about the origin of the universe dont you? So there would not be a hamster to go back in time. Also, hamsters are phyiscal entities and therefore require space but space didnt exist.


Quote:
(cracks that seawater flows through to produce ocean-floor hot springs)
Ed:
And as I stated earlier I am not a geologist, but possibly geologists will find out that they were bigger in the past.

lp: And possibly there was no planetwide Noah's Flood.
Possibly.


Quote:
(lots of nasty pathogens and parasites...)
OC:
Well you have to remember that after Man rebelled against the king of the universe(Genesis 2) there were immediate repercussions throughout the universe and it started malfunctioning. And things that were once good including man himself became corrupted. So these organisms may have originally been symbionts or may have only parasitized animals because of Man's perfect immune system at the time. But after Man's rebellion they microevolved into more pathogenic versions of themselves and Man became more susceptible to disease after he could no longer eat of the Tree of Life that protected him from death and disease.

lp: Ed evades the question of how Noah and his family had carried all these nasty bugs, since they had supposedly been created during the original time of creation. Their trip on the Ark might have been a great opportunity to rid the planet of these diseases. Also, that seems very vindictive of a supposedly loving being. If I sadistically beat you up and broke several of your bones just because you had called me some insulting name, would you say that I am perfectly loving?
See my post to OC. Your analogy is inadequate to explain God's justice. A better analogy would be that I was in the progress of laying the groundwork for something 1000 times worse than the Nazi Holocaust. What kind of punishment would I deserve?


Quote:
OC: So please define 'loving'.
Ed:
God is loving but also his moral character demands justice. And according to God, rebellion against him can only be justly punished by immediate death, but God in his mercy and lovingkindness did not immediately kill Man but instead the universe became corrupted and abnormal and was no longer a perfect home for Man so that is when these pathogenic organisms began microevolving. But also it allows humans time to repent of their rebellion and then will be allowed to live in the new earth and universe after this universe comes to an end.

lp: That is still vindictive. Ed, in the example above, would me letting your live be considered proof that I'm a perfectly loving being?
See my more accurate analogy above.


[b]
Quote:
Mr. Darwin quoting a common apologetic:
"God used ancient people as his writers of the scripture and much of it is written from their perspective."
Ed:
Yes, that is true, though I have yet to see that argued in a biblically persuasive way. But even if it was, my primary reason for rejecting Darwinian evolution is not theological in nature but scientific.

lp: But if someone deduced evolution by natural selection from the Bible, would you take that derivation seriously?

</strong>
If it was based on sound hermeneutics then yes I would.
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Old 04-29-2002, 11:11 PM   #324
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Quote:
Ed:
As I demonstrated in the EOG thread a superintelligent hamster in your basement can be logically eliminated as creator of the universe.

lp: However, if that hamster is capable of reaching back in time and creating some initial quantum singuarlity or whatever, it could do the job.
Ed:
How could he reach back in time if he didnt exist? ...
There you go again, O Ed. I don't see how there is supposed to be a time-travel brick wall at the moment of one's conception.


Quote:
(lots of nasty pathogens and parasites...)
Ed:
Well you have to remember that after Man rebelled against the king of the universe(Genesis 2) there were immediate repercussions throughout the universe and it started malfunctioning. ...

lp: Ed evades the question of how Noah and his family had carried all these nasty bugs, since they had supposedly been created during the original time of creation. Their trip on the Ark might have been a great opportunity to rid the planet of these diseases. Also, that seems very vindictive of a supposedly loving being. If I sadistically beat you up and broke several of your bones just because you had called me some insulting name, would you say that I am perfectly loving?
Ed:
See my post to OC. Your analogy is inadequate to explain God's justice. A better analogy would be that I was in the progress of laying the groundwork for something 1000 times worse than the Nazi Holocaust. What kind of punishment would I deserve?
And why is that supposed to be a good analogy, O Ed?

And I notice that you evaded the question of how Noah and his family managed to carry such a big load of pathogens and parasites. Or were they all the result of superfast evolution after the Flood?

Quote:
lp: But if someone deduced evolution by natural selection from the Bible, would you take that derivation seriously?
Ed:
If it was based on sound hermeneutics then yes I would.
That's very generous of you, O Ed.
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Old 04-30-2002, 03:31 AM   #325
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Further research and some help from a palaeontologist friend means I have more to report.

Mr Ed, the Talking Creationist, spake:

Quote:
Also, if you are referring to James Hopson's Therapsid Series, his series
is problematic.
Says who? In any case, the "therapsid series" is not simply something that Jim Hopson dreamt up. There is a very extensive literature on stem-group synapsids (= ‘mammal-like reptiles’, the group that includes the therapsids, as well as the more primitive pelycosaurs such as Dimetrodon), representing the work of dozens of different scientists, and all agree that these animals form the ancestral line to mammals.

Quote:
There is also the possibility that the mammal-like reptiles which have left no living representatives might have possessed features in their soft biology completely different from any known reptile or mammal which would eliminate them completely as mammal ancestors
Quite so. It is also possible that your late great-uncle Fred was actually an alien who only looked human but had a completely different biology.
&lt; looks to the audience, shrugs exasperatedly &gt; Seriously, does this guy have ANY understanding of how science works? You have to go by the actual data!

In this particular case, all the known attributes of mammal-like reptiles (preserved hard anatomy, bone histology) indicate unambiguously that they form the ancestral group for mammals. Their soft biology is simply unknown (except in so far as we can draw inferences about it from the skeleton), and there is nothing more that can be said about it. Period. To try to use imagined non-mammalian characteristics, for which there is no direct or indirect evidence at all, as evidence against a mammal-therapsid relationship is simply laughable. Even creationists usually manage to do better than that.

Quote:
just as the discovery of the living coelacanth revealed features in its soft anatomy which were unexpected and cast doubt on the ancestral status of its rhipidistian relatives.
No surprise that Ed has misunderstood this story. It is true that Latimeria proved to have some unexpected features, notably on the physiological front (it achieves osmotic balance with the surrounding sea water by concentrating urea in its blood, in the same way as sharks), but it also has some strikingly tetrapod-like features. Notably, it retains a vestigial lung (now filled with fat and functioning as a buoyancy organ) and a pulmonary vein, which strongly suggests that it had ancestors for whom air-breathing was significantly relevant. Molecular phylogenetic analyses (based on DNA sequences) also place it close to lungfishes and tetrapods.

In any case, ‘rhipidistians’ are actually a lot more tetrapod-like than coelacanths in their skeletal anatomy, and include obviously transitional forms like Panderichthys; their ancestral status is in no sense affected by the physiology or whatever of Latimeria.

So much for this particular missive; but does Ed not realise that he totally contradicts his earlier statement here?

Quote:
...as far as fish becoming reptiles, the lack of fossil specimens intermediate between anurans or urodeles and the older amphibians has forced paleontologists to base their speculations about the evolution of the group upon evidence from the anatomy and embryology of modern species which is a highly questionable practice.
So which is it going to be, Ed? If using evidence from modern organisms to draw inferences about relationships is "a highly questionable practice", then Latimeria is irrelevant to the problem of tetrapod origins. If Latimeria is relevant (as you obviously believe) then your criticism of modern-species data is unfounded. You can't have it both ways.

Of course, it is not at all "questionable" to use information from living creatures to reconstruct the relationships and evolution of a group; on the contrary, it is the very foundation of systematic biology. Fossils give us a direct glimpse into the past, but they can never yield as much information as living organisms because soft tissues, physiology etc are not preserved. Ed is simply demonstrating his ignorance here.

Looking at Ed’s claim in a bit more detail, note that the question of finding intermediates between anurans (frogs and toads) and urodeles (salamanders and newts), and "older amphibians" (what palaeontologists would call ‘early tetrapods’), is only tangentially relevant to the move from water to land (‘fish becoming reptiles’). As should be apparent, the move onto land was something that happened during the evolutionary transition from fishes to early tetrapods, ie at the origin of Ed’s "older amphibians" (which is why they are referred to as "older amphibians", not "older fishes"... simple when you think about it...).

Whether there is a gap in the fossil record between these "older amphibians" and the anurans and urodeles is irrelevant to the question of whether tetrapods evolved from
fishes. Just to give a few more details on these two topics:

Tetrapods evolved from fishes during the Devonian period, about 365-355 million years ago. The fossil record of this transition is rather good, and new discoveries are being made all the time. Key steps in the transition are represented by:

1) Osteolepiform fishes, of which Eusthenopteron is the best known. These are one of the subsets of Ed's "rhipidistians"; they have a normal fish shape and seen to have been entirely aquatic, but have certain tetrapod features in their anatomy such as paired fin skeletons containing equivalents of the limb bones humerus/femur, radius/tibia and ulna/fibula.

Eusthenopteron



2) Panderichthys. This form has all the tetrapod characteristics of osteolepiforms, plus a few more. It also has a crocodile-like head and body form with reduced fins, suggesting that it operated in very shallow water and maybe made short journeys over land. Panderichthyids and all other osteolepiform fish had a hole (choana) between the nasal passage and the mouth, which allowed air to pass from the nose into the mouth which is not present in other lobe-finned fish. Panderichthys also had external nostrils which were in the same position as those of the early tetrapods. The skull bones of these fish are bone for bone equivalents to the skull bones of the earliest tetrapods, and the braincase is so similar to earliest tetrapod ones that they were originally classified as tetrapods until a complete skeleton was found.

Eusthenopteron and Panderichthys



3) A fish similar to Sauripterus (Daeschler and Shubin (1998): Nature vol 391 no 133). Inside its fins are eight ‘fingers’ attached in a similar way to the digits of the earliest amphibians. Note that some early amphibians also had eight digits.



3) Ichthyostega and Acanthostega. These are the earliest tetrapods known from complete skeletons. They have limbs (with seven or eight digits apiece, rather than five), but retain tail fins, lateral line canals (sensory organs that only work in water) and a number of other fish characteristics. Both have external nostrils and choana; Acanthostega also has internal gills.





After the Devonian, the tetrapods (Ed's "older amphibians") lost their last few fish characteristics and diversified rapidly into a number of groups. One of these was the reptiles. The origin of reptiles is fairly well understood; the earliest reptiles (such as Hylonomus) are Late Carboniferous in age (about 300my) and very similar to some of
the "older amphibians" such as gephyrostegids and seymouriamorphs. The origin of lissamphibians (= anurans, urodeles and caecilians) probably occurred during the Permian, about 280 million years ago. The anurans are very similar to an "older amphibian" group called the temnospondyls, and almost certainly derives from these; there is a Triassic fossil from Madagascar, Triadobatrachus, that is neatly intermediate between temnospondyls and early anurans. The origins of the urodeles and caecilians ("worm amphibians") are less well understood. These groups are structurally very modified, and also have a poor fossil record (essentially because they are small animals), which makes them more difficult to position. However, they have a lot of characteristics in common with the anurans, and are clearly related to them, so most probably they too have a temnospondyl ancestry.

All plus more of which can be found here:
<a href="http://www.glenn.morton.btinternet.co.uk/transit.htm" target="_blank">http://www.glenn.morton.btinternet.co.uk/transit.htm</a>

And most of it was covered in the <a href="http://www.mdgekko.com/devonian/intro.html" target="_blank">Devonian Times</a> link I gave previously. Which shows that Ed isn’t reading what we offer him, and that he has no excuse for not knowing what the hell he’s talking about.

DNFTT & TTFN, OC
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Old 04-30-2002, 05:24 AM   #326
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Oolon: <img src="graemlins/notworthy.gif" border="0" alt="[Not Worthy]" /> <img src="graemlins/notworthy.gif" border="0" alt="[Not Worthy]" />

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Old 04-30-2002, 05:54 AM   #327
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A couple of missed points:

Quote:
Creation expects microevolutionary subtle differences.
(Emphasis added to, well, emphasise that we’re not just talking about normal variation between individuals, but rather, inheritable variation that can lead to speciation and beyond -- remember that Ed defined a ‘kind’ as ~ Family.)

Nonsense. Please show where the bible says so. Creation has been forced to accept such ‘microevolution’ because to say otherwise is perverse even by their standards. Hence the old joke:
Macroevolution: Evolution that no reasonable person can deny.
Microevolution: Evolution that not even creationists can deny.

Quote:
Yes, but the whole point [of the Nature article] is to show erectus intermediary between humans and apes which is the same thing [as establishing relationships between erectus and apes].
Don’t be ridiculous. What would be the point of simply showing a connection between erectus and apes, when this is utterly uncontroversial except for people such as yourself. As the abstract (Nature (2001), 414(6864):628-31) says:

Quote:
Here we report differences in enamel growth that show the earliest fossils attributed to Homo do not resemble modern humans in their development. [...] Neither australopiths nor fossils currently attributed to early Homo shared the slow trajectory of enamel growth typical of modern humans; rather, both resembled modern and fossil African apes. We then reconstructed tooth formation times in australopiths, in the approximately 1.5-Myr-old Homo erectus skeleton from Nariokotome, Kenya, and in another Homo erectus specimen, Sangiran S7-37 from Java. These times were shorter than those in modern humans. It therefore seems likely that truly modern dental development emerged relatively late in human evolution.
It’s noting differences, not suggesting a connection. The connection is thoroughly established as far as palaeoanthropologists are concerned.

Quote:
But if they occupy the same ecological niche, and they do,
You know this how? Simply by coexisting, they cannot be occupying exactly the same niche. That’s basic -- very basic -- ecology. Except of course if one is driving out the other over a (possibly large) number of generations.

Quote:
then they cannot be ancestral to humans.
How does that follow? You do know how speciation occurs, don’t you? And anyway, the ones coexisting wouldn’t be ancestral, by definition, any more than fox terriers and Jack Russells would be ancestral one to the other. Let me spell it out. Recent. Common. Ancestor.

Quote:
It in fact implies that they [Java man] are just different looking homo sapiens like your dog skulls.
Please explain the logic underlying that conclusion.

Mind you, if you consider KNM-ER 1813


to be just a different-looking Homo sapiens, then I guess the more subtle differences between erectus and sapiens are mere nit-picking.

TTFN, Oolon
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Old 04-30-2002, 07:23 AM   #328
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And while I’m in the mood to eat up bandwidth...

Just wondering, Ed... if this:



is human, is this human too?











Please don’t concern yourself with what’s damaged, nor with the absent soft tissues. Based on what there is, is it human? Might they be related?

Oh, and to save me having to ask, please say why, specifically, you think so.

Oolon
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Old 04-30-2002, 07:03 PM   #329
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Quote:
Originally posted by Rimstalker:
<strong>

Ed: As I demonstrated in the EOG thread a superintelligent hamster in your basement can be logically eliminated as creator of the universe

Actually a better recap is that they became frustrated when they were unable to refute my argument and then forcibly transferred me to this thread and THEN went home.

Rim: BULLSHIT! The ONLY thing you demonstrated is your inability to state a position and defend it. We bacame "frustrated" when you started shifting goalposts, going off-topic, commiting flagrant logical fallacies, and refusing to deal with our counter-arguments. You were "forcably" transfered here in a rather commendable concession by the moderators to give you space to vent your off-topic ramblings about flood geology. To any OBJECTIVE observer, this is the accurate account of what happened.[/b]
Calm down Rim. I exaggerated a little about being "forced" to another thread, but if you check the EOG thread you will see that absolutely NONE of the discussions about the flood were initiated by me. And please specify any logical fallacies and refusing to deal with counter arguments. I have a hunch though you won't do it because they are not there.

[b]
Quote:
Rim: Actually, screw objective observers! I've started a thread on EoG about this very subject, trolling for opinions from theists, who may be tilting in your favor. You can look it over if you like:
A request of all theists

</strong>
Go ahead and let them judge.

[ April 30, 2002: Message edited by: Ed ]</p>
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Old 05-01-2002, 10:52 AM   #330
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Quote:
if you check the EOG thread you will see that absolutely NONE of the discussions about the flood were initiated by me
That is a fair enough point. However...

Quote:
And please specify any logical fallacies and refusing to deal with counter arguments. I have a hunch though you won't do it because they are not there.
I have a hunch that you are yet again not willing to practice what you preach, because if you check the thread yourself, you will see the falicious nature of your argument specified quite explicitly.

Quote:
Go ahead and let them judge
So far, we have one theist who agrees with me. Not many others were interested.
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