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Wednesday, 28 June 2023
Correcting professor Dave on the "edge of evolution"
Nothing simple about these beginnings.
Gifted Microbes Elevate the Case for Intelligent Design to the Entire Biosphere
Tuesday, 27 June 2023
John Money:a brief history.
John Money
File under "well said" XCIV
"We have just enough religion to make us hate, but not enough to make us love one another."
Jonathan Swift
The Hindu/Muslim rivalry:a brief history.
Hindu–Islamic relations
Interactions between the followers of Islam and Hinduism began in the 7th century, after the advent of the latter in the Arabian Peninsula. These interactions were mainly by trade throughout the Indian Ocean. Historically, these interactions formed contrasting patterns in northern and southern India. In the north, there is a long-standing historical influence from Muslim rulers and Christian rulers dating back to the Delhi Sultanate of the 13th century. The patterns of relationship between Hindus and Muslims have been different between north and south India. While there is a history of conquest and domination in the north, Hindu-Muslim relations in Kerala and Tamil Nadu have been peaceful.[1] However, historical evidence has shown that violence had existed by the year 1700 A.D.[2]
In the 16th century, the Mughal Empire was established. Under the Mughals, India experienced a period of relative stability and prosperity.[3] The Mughals were known for their religious tolerance, and they actively patronized the arts and literature. During the Mughal era, Indian art and culture thrived, with the construction of grand monuments such as the Taj Mahal and the Red Fort. While the Mughals fostered religious harmony and cultural advancements and nurtured Hindu scholars, poets, and artists, facilitating a dynamic cultural interchange that enriched both Islamic and Hindu traditions, there were instances of religious conflicts between the Mughals and the Rajput over control of territories. Aurangzeb was criticized for his policies of religious intolerance towards Hindus.[4][5]
During the 17th to 19th centuries, India was ruled by the British, who introduced a policy of divide and rule to maintain their control over the country.[6][7][8] The British also introduced a system of separate electorates, which further exacerbated the divide between the Hindu and Muslim communities.[9][10] The Indian Rebellion of 1857, also known as the First War of Independence, was a major uprising against British rule in India. The rebellion was fueled by a range of grievances, including economic exploitation, social and religious discrimination, and political oppression.[11][12][13] While the rebellion was not solely based on religious tensions between Hindus and Muslims, these tensions did play a role in fueling the conflict. During the rebellion, there were instances of both Muslim and Hindu soldiers and civilians fighting together against the British, as well as instances of conflict between the two communities.[14][15][16]
Islam and Hinduism share some ritual practices, such as fasting and pilgrimage, but their views differ on various aspects. There are also hundreds of shared ritual spaces, called dargahs (literally, “doorway” or “threshold”), for Hindus and Muslims. These mark shrines for revered Muslim (frequently Sufi) leaders and are visited by both Muslims and Hindus. Their interaction has witnessed periods of cooperation and syncretism, and periods of religious discrimination, intolerance, and violence. As a religious minority in India, Muslims are part of the Indian culture and have lived with Hindus for over 13 centuries. Despite the longtime assertion that the origins of Muslim-Hindu tensions were greatly attributed to 19th Century British colonial rule in India, it has been argued that Britain had little influence on constructing the religious identities of Islam and Hinduism in the region and that divisions existed beforehand as well.[17] For example, 18th-century Mughal–Maratha Wars. Ajay Verghese argues that the Hindu-Muslim conflict in India can be better understood by analyzing the historical relationship between the two communities. He contends that precolonial India was marked by a fluidity of religious identity and that religious boundaries were not always clear-cut. This led to a degree of intermingling between Muslims and Hindus, but also created conditions for tension and conflict.[2]
Ps. What I would add is that most of these "religious" rivalries are really political rivalries masquerading as religious rivalries.
Darwinists' problem is not with design but the designer.
New Study Reveals How the Shape of My Nose Arose
It is ironic that Charles Lyell, whose seminal, if flawed, work in geology—the barrister is sometimes known as the father of modern geology—positively influenced Charles Darwin’s development of evolutionary theory—the young Darwin read Lyell’s book as he sailed around the world in the H.M.S. Beagle—and who helped to arrange for Darwin’s first formal, if awkward, presentation of his theory—an event precipitated by Wallace’s Ternate letter—was one of the last of the intelligentsia to accept Darwin’s new formulation of Epicureanism, known as evolution.
At one point an exasperated Darwin asked Lyell—it always comes down to metaphysics—if he believed “the shape of my nose was designed?” If Lyell did think so then, Darwin added, “I have nothing more to say.” The infra-dignitatem, or infra-dig for the irreverent, argument, which insisted that it was beneath the dignity of the Creator to stoop so low as to dwell in the details of the world, had been promoted by no less than the father of natural theology John Ray and Platonist Ralph Cudworth, and in Darwin’s day was in full swing. Its influence on the young Darwin was clear in the naturalist’s early notebooks, and here in his appeal to Lyell. One look at one’s nose is all one needs to know about origins. Obviously we evolved. Now, a century and a half later, science finally has its say in the matter.
A new Study out of, appropriately enough, England, now reveals the underlying genetic details that influence the shape of our noses. It seems there are four genes that influence the width and length of our olfactory device and, as the press release informs us, “The new information adds to our understanding of how the human face evolved.”
We are free to acknowledge free moral agency
Free Will: What Are the Reasons to Believe in It?
A theory of devolution?
Is Adaptation Actually a Fight to Stay the Same?
On a new episode of ID the Future, host Casey Luskin talks with Eric Anderson on location at this year’s Conference on Engineering and Living Systems (CELS). The two discuss an intriguing new engineering-based model of bounded adaptation that could dramatically change how we view small-scale evolutionary changes within populations of organisms. In presenting his argument for natural selection, Charles Darwin pointed to small changes like finch beak size and peppered moth color as visible evidence of an unguided evolutionary process at work. Many have adopted this perspective, quick to grant the Darwinian mechanism credit for micro-, if not macro-, evolution. But Anderson and other attendees at the CELS conference are starting to promote a different view. “We need to stop saying organisms are partly designed,” says Anderson. “We need to view them as deeply designed and purposeful, active and engaged in their environments, and capable of adapting within their operating parameters.” To get a fascinating glimpse of this novel approach to biology, download the podcast or listen to it here .
Monday, 26 June 2023
On professor Dave and the bacterial flagellum
Answering Farina on Behe’s Work: Bacterial Flagella
In a previous article, I began a series of four responses to YouTuber Dave Farina (aka “Professor Dave”) about his video reviewing Dr. Michael Behe’s three books. Here I will turn my attention to Mr. Farina’s comments regarding bacterial flagella.
In relation to the flagellum, the video complains about Behe’s “dishonest usage of terminology pertaining to machinery,” including phrases such as “outboard motor,” “drive shaft,” “universal joint,” “bushings,” and “clutch and braking system.” In reality, this terminology is used widely in the scientific literature. It’s not unique to Behe. On the contrary, in reference to flagella, the literature is full of such terms including “motor”,1 “drive shaft,”2 “universal joint,”3“bushing,”4 and “clutch.”5 The word “machine” itself has a wide circulation.6 Is Farina going to charge the entire flagella research community with dishonesty as well?
Co-option Scenarios for the Origins of Bacterial Flagella
According to the video, “A flagellum that merely twitches instead of rotating smoothly would also produce motion and thus could be selected for.” But a type IV pilis, which enables twitching motility (a form of bacterial translocation over moist surfaces), is very different from a flagellum. Twitching motility occurs by extension, tethering, and retraction of the type IV pilus, which functions in a manner akin to a grappling hook. A flagellum, on the other hand, rotates as it is driven by a proton motive force across the cell membrane. The assembly mechanisms of pili and flagella are also quite different.
The video complains that Behe fails to acknowledge the existence of alternative flagellar systems that are simpler than the model system found in Salmonella species and Escherichia coli. However, the fact that an alternative system lacks a specific component that is essential in another system does not mean that the former lacks an alternative mechanism for achieving the same outcome. The most robust concept of irreducible complexity understands it as a property of a system that is contributed to by multiple subfunctions, the removal of one of which causes the overall system to effectively cease performing its job. Note that each individual subfunction could, in principle, be performed by multiple protein components. Likewise, a single protein component could perform more than one of those subfunctions. Furthermore, the identity of the specific components performing each respective subfunction could differ from one organism to the next. It is therefore not the identity of the structural parts that is important in an irreducibly complex system, but rather the essential functions that need to be performed in order for a higher-level objective to be realized.
Moreover, pointing to homologues of flagellar proteins does not undermine the argument from irreducible complexity, since co-opting those proteins to produce a flagellar system requires multiple co-incident changes in order for the new system to be realized. For example, flagellar-specific proteins would not confer a selective advantage until incorporated into the flagellar system. But the necessary proteins that serve roles in other systems will not become incorporated into the flagellar system before these flagellar-specific proteins arise. This is quite aside from the need to have complementary protein-protein binding interfaces, as well as a choreographed assembly system to ensure that the proteins are assembled in the appropriate order.
Resurrecting a Flagellum
In a 2016 article at Evolution News, Behe asks,
W]hy doesn’t [Kenneth Miller] just take an appropriate bacterial species, knock out the genes for its flagellum, place the bacterium under selective pressure (for mobility, say), and experimentally produce a flagellum — or any equally complex system — in the laboratory? (A flagellum, after all, has only 30-40 genes, not the hundreds Miller claims would be easy for natural selection to rapidly redesign.) If he did that, my claims would be utterly falsified. But he won’t even try it because he is grossly exaggerating the prospects of success.
The video by Farina comments,
hilariously, [Behe] is oblivious to the fact that this precise experiment was carried out the year before. Here’s the paper. Gene deletion produced two strains of bacteria with no flagellum. They then introduced selective pressure for motility by depleting the nutrients in the colony. Within 96 hours, both strains had regenerated flagellar motility by a pathway involving two successive point mutations in genes that served other purposes.
However, the paper that Farina cites7 does not do this at all. Not for the first time with this video, I wonder if he has in fact read the paper. All that the researchers deleted was the flagellar master switch protein, FleQ, in Pseudomonas fluorescens. After a few days of incubating the bacterial cells on Petri dishes, they reacquired their ability to grow flagella. The genetic basis for this reactivation of the flagella is that another master switch protein, NtrC, that is a structurally similar homolog of FleQ — responsible for turning on genes involved in nitrogen metabolism — already had the ability, to some extent, to cross-bind to the promoter usually bound by FleQ. When produced in excess, as a result of a broken regulator, NtrC was thus able to drive flagellar synthesis. As a consequence of this mutation, the bacterial cell lost its ability to regulate its nitrogen metabolism genes. An article in The Scientist describes this research:
But while the re-evolved flagella enabled the bacteria to access food supplies at the farthest reaches of the Petri dish, the ability came at a price. ‘The bacteria that became much better at swimming were much worse at nitrogen regulation,’ said Johnson. However, she added, ‘sometimes the advantage can be so great that it’s worth paying that cost because otherwise you die.’
Thus, contrary to the Farina video’s claims, this paper does not document the de novo evolutionary origins of a bacterial flagellum at all — far from it. In fact, Behe has already addressed the paper here.
The Waiting Times Problem
In 2004, Michael Behe and David Snoke published a paper in the journal, Protein Science.8 About this paper, Farina has three complaints. The first complaint is that, “Behe and Snoke found that the target sequence did actually evolve, in population sizes and timeframes that are entirely realistic, and if anything, quite small compared to real-world populations. The paper literally proves them wrong and they somehow count it as a win anyway.” Farina mentions Behe’s expert testimony at the 2005 Kitzmiller v. Dover trial:
When questioned about his 2004 paper, Behe tacitly acknowledged that the population size in their model was orders of magnitude smaller than real-world bacterial populations, which had the effect of vastly underestimating the rate at which such “irreducible” traits could evolve… In one striking exchange, Behe acknowledged a paper which indicated that there are more prokaryotes in a single ton of soil than in his model population, and that there is a lot more than one ton of soil on Earth.
However, this objection stems from Farina’s misreading of the paper. As Behe himself explains in the very transcript that Farina cites, “forming a new disulfide bond might require as few as two point mutations. But forming other multi-residue features such as protein-protein binding sites might require more.” The graph below (figure 6 of the paper) shows Behe and Snoke’s estimate of the time to fixation (along the y-axis) versus the number of substitutions needed for a new feature to evolve (along the x-axis). On the top axis, values for the needed population sizes are given. The point is that, as the number of needed co-dependent mutations increases, so too does the needed population size and waiting time to fixation.
As Behe and Snoke explain in the paper, in a scenario where three substitutions are required for a novel feature to arise, a population size of roughly 1011 individuals is necessary for it to become fixed over the course of 108 generations (108 generations is marked as a horizontal bar on the figure). If the complex trait in question requires even more substitutions, it would require considerably more time. If six mutations were needed, the average population size required for it to become fixed in 108 generations would be on the order of 1022 individuals. Given that 1030 is a plausible estimate of the number of microorganisms on the entire planet9, these numbers become prohibitive very quickly.
The second complaint is that, “In their model, Behe and Snoke permitted only single-base mutations and natural selection — no recombination, no duplications beyond the initial presumed one, no other evolutionary changes.” But the authors explicitly say that “Because the model presented here does not include recombination, the results can be considered to be most applicable to a haploid, asexual population.” Nonetheless, they do note in the conclusion to their paper that “the results also impinge on the evolution of diploid sexual organisms,” since large multicellular organisms have much, much smaller population sizes than bacteria. If the evolution of complex features is difficult for microorganisms (with their massive population sizes and short generation turnover times), how much more so for large animals? Though one might counter, in the case of diploid sexual species, that recombination allows for neutral mutations to occur separately in a population and to later combine by sexual recombination, Christiansen et al. have shown, in a paper published in Theoretical Population Biology, that “Recombination lowers the waiting time until a new genotypic combination first appears, but the effect is small compared to that of the mutation rate and population size” (emphasis added).10
Finally, Farina complains that “They also specified a pre-determined target sequence and only considered the simulation to have been ‘successful’ if that specific target evolved.” But this is incorrect. Rather, the paper provides estimates for how many organisms would be required, and over how long a time frame, for multiple co-dependent mutations (none of which by themselves confers an advantage) to become fixed in a population.
Notes
Minamino T, Imada K, Namba K. Molecular motors of the bacterial flagella. Curr Opin Struct Biol. 2008; 18(6):693-701.
Johnson S, Furlong EJ, Deme JC, Nord AL, Caesar JJE, Chevance FFV, Berry RM, Hughes KT, Lea SM. Molecular structure of the intact bacterial flagellar basal body. Nat Microbiol. 2021; 6(6):712-721.
Kitao A, Hata H. Molecular dynamics simulation of bacterial flagella. Biophys Rev. 2018; 10(2):617-629.
Yamaguchi T, Makino F, Miyata T, Minamino T, Kato T, Namba K. Structure of the molecular bushing of the bacterial flagellar motor. Nat Commun. 2021 Jul 22;12(1):4469.
Blair KM, Turner L, Winkelman JT, Berg HC, Kearns DB. A molecular clutch disables flagella in the Bacillus subtilis biofilm. Science. 2008;320(5883):1636-8.
Sowa Y, Berry RM. Bacterial flagellar motor. Q Rev Biophys. 2008 May;41(2):103-32.
Taylor TB, Mulley G, Dills AH, Alsohim AS, McGuffin LJ, Studholme DJ, Silby MW, Brockhurst MA, Johnson LJ, Jackson RW. Evolution. Evolutionary resurrection of flagellar motility via rewiring of the nitrogen regulation system. Science. 2015; 347(6225):1014-7.
Behe MJ, Snoke DW. Simulating evolution by gene duplication of protein features that require multiple amino acid residues. Protein Sci. 2004; 13(10):2651-64.
Whitman WB, Coleman DC, Wiebe WJ. Prokaryotes: the unseen majority. Proc Natl Acad Sci U S A. 1998; 95(12):6578-83.
Christiansen FB, Otto SP, Bergman A, Feldman MW. Waiting with and without recombination: the time to production of a double mutant. Theor Popul Biol.1998;53(3):199-215.
Sunday, 25 June 2023
How hubris sinks the unsinkable.
Shades of Titanic — Probing the Wreck of the Unsinkable Enlightenment
The week that the submersible Titan was revealed to have been instantaneously flattened on its way down to the wreck of the Titanic, David Berlinski spoke with Jame Lileks and Peter Robinson on Ricochet about the wreck of the Enlightenment. Much like the Titanic, and a bit like the Titan, so much was expected at the glorious launch of the experiment in human reasoning — yet down it went to disaster, not least in the 20th century with its horrors.
Writing yesterday in the Wall Street Journal, Peggy Noonan suggested that the story of the Titanic haunts us in part because its demise came two years before the start of the century’s great catastrophe, World War I: “the reason the Titanic endures is that there was an immediate connection in the public mind with the Great War. The 20th century was to be the century of progress.” Interesting connection. Science and reason were supposed to transform the world for the good instead of soaking it in gore. In his books — Human Nature and his latest, Science After Babel — Berlinski probes the causes behind that failure. “A cold wind is blowing,” the mathematician and philosopher observes, revealing how “fragile” the Enlightenment dream really was. The conversation with Dr. Berlinski begins at 31:45.
Saturday, 24 June 2023
Speaking of ID...
How to Discuss Intelligent Design with Friends
On a classic episode of ID the Future, Tom Gilson — author, senior editor with The Stream, and occasional contributor to Evolution News — tackles the question of how best to discuss intelligent design (ID) with friends and associates skeptical of the theory. There is so much misinformation about the theory of ID that many well-intended people reject not the actual theory but a silly caricature, a straw man. They don’t realize that ID is not an argument from ignorance but an inference to the best explanation based on positive evidence for design and negative evidence against competing materialistic explanations. It involves abductive reasoning, a standard mode of reasoning in the historical sciences. When in conversation with someone who understands none of this, Gilson suggests using the Socratic method and, in particular, posing three questions designed to turn down the heat, promote dialogue, and draw the other person into a discovery of the actual theory of intelligent design. Try it with friends, colleagues, and family members! Download the podcast or listen to it here
Friday, 23 June 2023
No Jehovah,no Justice,no Peace here's why.
The pseudo-religious bureaucracies of this age have given religion/worship a bad name.Likely many would agree with Indian statesman Jawarlal Nehru when he said that the spectacle of organised religion in India and elsewhere filled his mind with horror,and that it seems almost always to stand for superstition,ignorance,bigotry,exploitation,the vested interest of entrenched elites and the like.But long before Nehru now famous religious leader/teacher Jesus Christ had some choice words for the leaders of the dominant religion of his time and place: Matthew23:13KJV "But woe unto you scribes and pharisees,!For ye shut up the kingdom of heaven against men:For ye go in yourselves,neither suffer ye them that are entering to go in.Woe unto you,scribes and pharisees,hypocrites!For ye devour widows houses,and for a pretence make long prayer:Therefore ye shall receive the greater damnation.
Two things to note in Jesus censure 1)The hypocrisy of these religious leaders separated them from God 2)Their hypocrisy turned others away from the God's truth.How?The bible suggest two ways 1)Matthew23:15ESV "Woe to you, scribes and pharisees,hypocrites!For you travel across sea and land to make a single proselyte,and when he becomes a proselyte,you make him twice as much a child of hell as yourselves."
2)2Peter2:2 "Many will follow their sensuality,and because of them the way of truth will be blasphemed."
On account of its bringing his name and kingdom into disrepute pseudo-religion in general and Christendom in particular is in the cross hairs of Jehovah's war machine.The bible tells us that soon pseudo-religion will pay a heavy price for its political meddling, greed and hypocrisy.Revelation19:2"because His judgments are trued and righteous,e
because He has judged the notorious prostitutef
who corrupted the earth with her sexual immorality;
and He has avenged the blood of His •slaves
that was on her hands.g"
There are of course those who urge an abandonment of the quest for the creator God.They claim that accepting a status of cosmic orphanhood and making new gods of chance,necessity,matter and self are the only way to free ourselves from the abuses of the past.To begin with militant atheist have been every bit as unsuccessful on liberating their flock from the racism,nationalism,militarism and greed that have always been the main triggers of conflict as theistic pseudo-religionists have.Additionally there are practical reasons that universal justice and peace are simply not possible apart from Jehovah's assertion of his rightful sovereignty over the globe
1)Only Jehovah as creator can claim unimpeachable legitimacy as a global governor,there plain and simply is no man or group of men(or angels for that matter)that can be trusted with that kind of authority,apart from the fact that it is a universally accepted legal principle that the creator be recognised as legal owner of what he has produced.Jehovah is totally independent of his creation and is thus morally incorruptible,What could anyone possibly offer him as a bribe?A new luxury car?Tickets to the big game?A case of champagne perhaps?With him in charge mankind will finally have a ruler worthy of utter confidence and loyalty.
2)Jehovah is not learning on the job the very wisest among us human or superhuman is only just beginning to understand how to get the most out of Jehovah's creation Jehovah has been there and done that so to speak.No more guessing games with people's lives,health and prosperity.
3)Only Jehovah has the might/smarts to bring leviathan and his hordes to heal.There is a reason that the criminal and otherwise sociopathic elements of society always seem ahead of the agencies charged with countering them.Why instead they have consistently succeeding in corrupting the wider society.Some might be prepared to acknowledge behind the scenes influences on the human level.They might be less willing to acknowledge the Bible's warning that the corruption of the main institutions of our global civilisation extends to the realm of the superhuman see Ephesians6:12.Until our civilisation is rid of these malignant minds human and superhuman advances in technology will continue to be more of a curse than a blessing.
4)Only Jehovah can guarantee infallible judgement.Not only is he first hand witness to all wrongdoing and right doing he can read hearts.This means that under his rule not only will we finally have a ruler worthy of our complete trust we will have fellow servants worthy of our complete trust.Picture a society with no need for
police,soldiers,spies,security personnel of any kind,courts,magistrates,judges,jails,locks,keys.Impossible you say?Certainly in the atheistic universe we could entertain no such hope.
5)Justice delayed is Justice denied the saying goes.What about when justice never arrives?The number of unsolved crimes on the files of this world's law enforcement agencies is in the tens of thousands some of these are horrific indeed heartbreaking murders.What about those who have been erroneously convicted crimes they never committed What about past victims of state sponsored injustice.Jehovah is not only mankind's only hope of a just future he ALONE can counter the injustices of the past.
What is a hominid?
Fossil Friday: To Be or Not to Be Homo
The fossil hominin Homo habilis was described 1964 by famous paleoanthropologist Louis Leakey and his colleagues from the 1.9 million year old Olduvai Gorge locality in Tanzania (Leakey et al. 1964). Even though this taxon is only known from a small and highly incomplete collection of isolated bone fragments, it has become the crucial hominid species that supposedly bridges the gap between the ape-like australopithecines and our human genus Homo. Because of the association of the bones with stone tools it has been named Homo habilis, which means “handy man.” However, its alleged position as transitional form is quite controversial (also see Gibbons 2011, Luskin 2007, 2015), and even the validity of the species has been questioned because it seems to be “a wastebasket taxon, little more than a convenient recipient for a motley assortment of hominin fossils” (Tattersall 1992). Homo habilis certainly was not the ancestor of later Homo species, because he is too recent and coexisted with early Homo ergaster, thus leaving a distinct gap between australopithecines and the genus Homo (Hawks et al. 2000).
A Dubious Attribution?
Since its small brain volume falls within the range of australopithecines, several scientists very early doubted the attribution of H. habilis to the genus Homo. Also the hand and feet are more ape-like and exhibit clear adaptations for climbing. Walker & Shipman (1996: 132) said that H. habilis is even more ape-like than Lucy, and Spoor et al. (1994) even remarked in their comparative study of hominid labyrinthine morphology that “The specimen Stw 53 provisionally attributed to H. habilis, differs from all other hominids … [and] shows greatest similarities to the pattern observed for large cercopithecoids …[which] suggest that Stw53 relied less on bipedal behaviour than the australopithecines”. Holly Smith (1994) concluded from the comparative study hominid patterns of dental development that gracile australopithecines and H. habilis remain classified with African apes. Wood & Collard (1999a, 1999b, 2001), Collard & Wood (2007, 2015) could show that in none of the crucial character H. habilis is closer to Homo than to Australopithecus.
An Assignment Rejected
Therefore, they suggested that H. habilis should be transferred to the genus Australopithecus, which was also supported by Hartwig-Scherer (1999) and Schwartz & Tattersall (2015). This assignment was rejected by Harcourt-Smith (2007) based on postcranial characters, while Berger et al. (2015) agreed that “postcranial remains of H. habilis appear to reflect an australopith-like body plan”. Spoor et al. (2015) found that the mandible of H. habilis is remarkably primitive and more similar to Australopithecus afarensis. They also reconstructed a slightly larger brain volume for the holotype and clarified the definition of the taxon Homo habilis, but cautioned that the results raise questions about its phylogenetic relationships. It is also very much contradicting Darwinian expectations, that the oldest specimens of Homo habilis, such as the 2.3 million year old specimen no. AL 666-1, possess more advanced characters than the younger holotype specimen OH 7, which lived more than a half million years later. One of the most striking contradictions is the fact that the bones of Homo habilis and many other animals were found in the context of so-called “butchering sites” together with stone tools, and in the neighbourhood of rock circles that very much look like the stone huts still used by modern nomadic tribes of the region (Leakey 1972: 24).
These rock circles and huts demonstrably originated at the same time as Homo habilis, which obviously suggests that this ape-like creature was rather the animal prey of contemporary human hunters than a human ancestor and producer of stone tools. Otherwise, we would have to believe highly implausible hypothesis that an ape-like creature with an ape-sized brain and climbing adaptations built stone huts like modern humans. Anyway, the majority of evolutionists of course ignored all such doubts among the experts and blindly embraced Homo habilis as a cherished “missing link” without asking inconvenient and potentially career-threatening questions.
Reference
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Natural antifreeze vs. Darwin.
Blood Viscosity and Freezing Temperatures — A Titanic Problem
Editor’s note: With the RMS Titanic tragically back in the news this week, we thought of this article from last year by biochemist Emily Reeves. She notes a question about the character Jack in the movie Titanic, and addresses a fascinating problem in marine biology.
Dr. Gregory Sloop is a Montana physician who knows a thing or two about the cardiovascular system. He has an article in the journal BIO-Complexity highlighting the sleek design of the Antarctic icefish that allows it to live in super-cold waters without freezing to death.
Icefish, aka the family Channichthydiae, survive at 0oC in the Southern Ocean by maintaining blood viscosity at the set point of 3.27 centipoise — a level nearly identical to human blood. They do this without hemoglobin, which is the primary determinant of human and other red-blooded animals’ blood viscosity.
Since icefish don’t have hemoglobin, how do they maintain blood viscosity? Also, how do they breathe? Turns out they maintain viscosity at freezing temperatures primarily by using a special type of glycoprotein: the antifreeze protein. And because oxygen has a higher solubility at lower temperatures, icefish don’t need an oxygen transport molecule like hemoglobin.
Why Jack Froze
In case you were wondering, blood viscosity is the technical reason why Jack (Rose’s buddy aboard the Titanic) froze in less than 23 minutes, but icefish can survive for 15 years in water of a freezing temperature. Viscosity increases at lower temperatures, and at 0oC human blood reaches a viscosity that is not compatible with life. This is because hemoglobin as a protein is not able to keep viscosity low enough at freezing temperatures. But the antifreeze protein can (think: custom design).
While a viscosity too high is incompatible with life, a low viscosity is also unsuitable for sustaining life. This is because a properly functioning cardiovascular system must have optimized laminar flow and low vascular resistance, which can be achieved only through coordinated control of blood viscosity and specification of vascular geometry.
Stop Criticizing Icefish
Dr. Sloop says icefish have been criticized for expending nearly 22 percent of their basal metabolic rate pumping their hemoglobinless blood compared to at most 5 percent in temperate fish. But he reminds his readers that’s just the cost of doing business in the chilly — well technically, freezing — waters of the Southern Ocean.
Sloop also emphasizes that everything about the icefish is like a custom-fitted suit — appropriate for niche needs. Features included for dealing with the extreme cold are a high-output, low resistance vasculature where the diameter of muscle capillaries is 2-3 times larger than those of other fish.
These fish also have a heavy heart which delivers a larger stroke and therefore higher volume. Together these features enable a high-output, high-velocity, low-pressure, and low-resistance circulation.
Truly, every part of these incredible creatures is optimized for cold. Could all these custom changes be the result of random mutation? Dr. Sloop thinks that is very unlikely. What do you say?
Comb Jelly's have never been a "simple lifeform"
Earliest Comb Jellies Wore Armor — “Remarkable,” Say Researchers
What does it take to wear armor? An animal has to be able to make the material and put it where it belongs. To be functional, the armor cannot interfere with the animal’s movement. And the animal cannot simply glue sand particles on its exterior in a haphazard way. The appropriate materials, directed by genetic instructions, must be manufactured and placed holistically so that the finished armor provides a beneficial function. It would be surprising, under an evolutionary view, to find such a complex system in the earliest animal fossils. But that’s what Chinese paleontologists discovered in their country’s early Cambrian rocks.
Phylum Ctenophora (cilia-bearing) has about 150 living representatives. While most of them have tentacles, none have hard parts. Varying in size from a few millimeters to over a meter, they resemble jellyfish (phylum Cnidaria) in being gelatinous and transparent, but are distinct in having eight-fold radial symmetry with comb-like rows of fused cilia that propel them around. Some living comb jellies give stunning light shows as their comb rows reflect light in rainbows of iridescent colors, making them resemble alien spacecraft.
Though not bilaterians, they have complex body plans with a buoyancy organ called a statolith, muscles, a nervous system, an alimentary canal, and the ability to control the direction of their locomotion. The phylum made its appearance in the earliest Cambrian layers, dated 520 million years ago. That takes us to the Chengjiang biota in China, one of the finest exposures of early Cambrian fossils in the world.
A Surprise for Fossil Hunters
Seven Chinese researchers found beautifully preserved comb jellies in lower Cambrian strata — three new species and three reclassified species — all with armor. Their open-access paper in Science Advances, “A vanished history of skeletonization in Cambrian comb jellies,” shows the photographs of the fossils along with diagrams of how they probably looked. Armored struts and plates are arranged in complex shapes along the animals’ exterior, following the eight-fold symmetry and making up complex curves. One of the species has spines along its outer struts. The fossil hunters were quite surprised:
They share a basic body plan characterized by a tentacleless and octaradial body with an oral-aboral axis, eight rigid struts (termed here “spokes”) radiating from the aboral end and arched to converge to the oral end, eight soft-bodied flaps or lobes supported by the spokes, eight pairs of ctene rows, a conspicuous apical (or aboral) organ walled by eight rigid plates and housing a spheroidal or ellipsoidal statolith, and an oral region surrounded by eight apiculate lappets…
The eight arcuate spokes [in one species] bear robust spines (Fig. 2, L to N, and figs. S4 to S6) and retain their structural integrity even when disarticulated, suggesting a remarkable degree of sclerotization.
The plates have “considerable rigidity,” they noticed, retaining their integrity even when separated. Some of the hard parts protrude into different layers of sediments. It’s not clear what the armor is made of, but the authors presume it is chitin, the same protein that makes up the exoskeleton of arthropods. “The spokes and apical plates of scleroctenophores were likely cuticular or chitinous in composition, but the presence of minerals in their skeletons cannot be completely ruled out, given that the epidermis of extant ctenophores can produce Mg-Ca carbonates that partially form the statolith,” they say. The statoliths of some fossil specimens even preserve some organic carbon.
Evolutionary Speculations
The authors are not sure about the function of the armor, but indulge in some evolutionary speculation. The typical evolutionary explanation is to imagine an “arms race” that forced the animals to defend themselves against a new class of predators. It seems obvious, though, that nothing about predation can cause a brainless animal to build a suit of armor. It could more easily just go extinct.
What’s even more remarkable (a word they use themselves) is that the ctenophores are not alone in being armored compared to living counterparts. They use this observation to support a view from the late Stephen Jay Gould that evolution is highly unpredictable:
The occurrence of sclerotized and armored skeletons in Cambrian representatives of several animal groups — including entoprocts, phoronids, lobopods, scalidophorans, and now ctenophores that are exclusively soft-bodied among modern survivors — is a remarkable phenomenon. The independent skeletonization among these diverse Cambrian animals provides indirect evidence for an intensified level of ecological interactions (for example, arms race) and also highlights the importance of paleontological data in illuminating the evolutionary legacy that would be otherwise inaccessible by studying living animals alone. The widespread occurrence of skeletonization echoes Stephen Jay Gould’s view of the striking morphological disparity of many animal phyla during their Cambrian debut, and the contrasting evolutionary trajectories of skeletonized cnidarians and ctenophores also elucidate the contingent fate of evolutionary innovations such as skeletonization.
Protection from Evidence
This kind of explanation serves only to protect Darwinian evolution from the evidence. If animals are similar, they evolved. If animals are different, they evolved. But the authors noticed that the “morphological disparity” in the Cambrian explosion exists not only between phyla, but between species within phyla. Earlier, they referred to the explosion:
Here, we report several sclerotized and armored ctenophore species, based on new material and reinterpretation of previously published material from the early Cambrian Chengjiang biota (ca. 520 Ma). Along with armored Cambrian entoprocts, phoronids, lobopods, and scalidophorans, the new fossils suggest a vanished Cambrian history of skeletonization in multiple animal groups, imply the ecological importance of skeletonization in the Cambrian explosion, and highlight the remarkable morphological disparity in certain Cambrian animal clades relative to their modern survivors.
A “vanished Cambrian history of skeletonization in multiple animal groups” is inconsistent with Darwinian evolution. “Ecological importance” is incapable of producing genetic programming for an armored skeleton. “Morphological disparity” at the earliest onset of complex animals is the opposite of Darwin’s image of a branching tree gradually separating into more and more complex types.
Designers, by contrast, know how to apply a common solution in different applications. That’s why it’s unsurprising to see complex armor in disparate groups from the beginning.
Stephen Meyer did not go into detail about ctenophores in Darwin’s Doubt, other than to note they are among the phyla that suddenly appeared in the Cambrian explosion (p. 32). But this revelation that ctenophores are more complex than originally realized, possessing elaborate armor, certainly reinforces his contention that “the best explanation for the explosion of information necessary for the Cambrian animals… remains intelligent design” (see the Epilogue in the paperback edition, p. 448).