Charles Darwin and the tower of Babel.

 Language: Darwin’s Eternal Mystery

Neil Thomas. 

In a previous contribution I expressed regret that the modern age did not have an outstanding satirist willing to take on overblown scientific pretensions of the stature of the early 19th-century satirical novelist Thomas Love Peacock. I recalled the magnificent quatrain he chose as the preface for his first novel, Headlong Hall (1816), which, although it was meant to lampoon ideas like phrenology belonging to his own age, would seem to fit the post-Darwinian era all too well: 

All philosophers, who find

Some favourite system to their mind

In every point to make it fit,

Will force all nature to submit.1

One can only speculate what Peacock (1785-1866) in his prime might have made of Darwin. His second novel, Melincourt (1817), featured an ape standing for Parliament under the name of Sir Oran Haut-ton, a spoof on the 18th-century speculation of the Scottish jurist Lord Monboddo (James Burnet) on the simian ancestry of mankind. But since the eccentric Monboddo’s ideas were commonly taken to be an elaborate joke born of intellectual diablerie, Peacock could not advance far beyond the slapstick element of his conceit to explore the deeper, metaphysical implications of Monboddo’s idea.

Enter Tom Wolfe

When I lamented the absence of such a writer as Peacock in the 21st century it must have temporarily slipped my mind that we do have a writer of a standing fully equal to that of Peacock in the shape of Bonfire of the Vanities author Tom Wolfe. In Wolfe’s The Kingdom of Speech (2016),2 published just two years before the author’s death, Wolfe took time out from his creative writing to focus on the everlasting crux of the origin of the human speech facility. It is a mystery which has puzzled humanity at least since the time of Johann Gottfried Herder in the 18th century and, as Wolfe points out with some humorous relish,3 the roots of the language facility remain as unknown now as they did when Herder wrote his Ueber den Ursprung der Sprache (On the Origin of Language) in 1772.

Neither Herder nor later Darwin, as Wolfe points out, could find one shred of evidence that human speech had evolved from animals. This was particularly galling to Darwin since his whole life was essentially a quest for the secrets of creation or, as Wolfe phrases it in more mordant tones, “Darwin had fallen, without realizing it, into the trap of cosmogonism, the compulsion to find the ever-elusive Theory of Everything, an idea or narrative that reveals everything in the world to be part of a single and suddenly clear pattern.” (p. 20)

Western and Native American Cosmogonies

In reviewing that fruitless human quest for explanations about origins, Wolfe appends an overview of native American cosmogonies, finding the Apache version of the creation of the whole firmament by a scorpion to be but a more colorful and imaginative version of “the currently solemnly accepted — i.e., ‘scientific’ — Big Bang theory, which with a straight face tells us how something, i.e. the whole world, was created out of nothing.” (p. 22)

Wolfe surely has a point. The current understanding of the universe’s origin — subject of course to no other, more convincing theory being advanced in my or your lifetime — is that about 15 billion years ago all mass and energy were compacted together but (for reasons equally unknown and doubtless forever unknowable) simply proceeded to inflate. Cosmologists, who are remarkably honest about their inability to illuminate the sheer unintelligibility of the cosmos (sometimes, it strikes me, even taking a perverse, mock- masochistic delight in the way it seems to cast out curve-balls in the way of human understanding4), concede that this originary event occurred “just like that” ­— without discernible rhyme or reason (that we or they can know of).

It can scarcely be denied that the Big Bang theory, despite its widespread acceptance by the scientific community and by the public at large (albeit passively), remains irredeemably problematic in logical terms: how can something come from nothing? It seems that the primal ka-boom lies quite beyond our conceptual bounds. Or, with reference to the older steady-state theory, how could something always have been there? The human mind at this point inevitably experiences what Chomsky once called “cognitive closure” — complete bafflement. We are left in the unenviable position of neither alternative making sense to us, both Big Bang and Steady State paradigms being equally overweighted by logic-defying anomalies.

The Big Bang theory is perhaps the more problematic of the two. To accept the proposition that an unregulated, chance explosion/expansion produced our terrestrial order is rather like buying into that old canard that the multiple volumes of the Oxford English Dictionary could have been produced by an explosion in an ink shop. If on the other hand the explosion had been very precisely calibrated (somehow, by a higher power unknown) in order to deliberately retrieve order from seeming chaos, then that premeditated deliberation would in good logic demand a designing originator, and this would make the Big Bang a story of creation in the fullest sense.5 That conclusion of course would tip us into the theological realm of discourse in quest of a logical explanation to cover the totality of known facts. For the idea of the whole universe-in-embryo compressed into the space of a single subatomic particle would count in most people’s book as a full-on miracle, barely if at all distinguishable from the Bible’s creation ex nihilo, and it is little wonder that advances in modern science have sometimes been read as confirmation of the Biblical account contained in Genesis.6 They have at the very least done nothing to disprove the Biblical narrative.

Science and Educated Guesswork

What is striking about Wolfe’s analysis is the intellectual equivalence he perceives between such narratives as George Lemaître’s Big Bang, Darwin’s “abiogenetic” theory of life emerging from chemical reactions in a small warm pond, and what he sees as broadly corresponding native American versions. All such theories are “educated guesses,” with minor differences to be explained by the shibboleths of modern science vis-à-vis the more uninhibited speculations of native peoples. So for instance “in the Navajo cosmogony the agent of change was alive. It was the Locust. In Darwin’s cosmogony it had to be scientifically inanimate [to escape charges of animism]. Locust was renamed Evolution…. Like every other cosmogony, Darwin’s was a serious and sincere story meant to satisfy man’s endless curiosity about where he came from and how he came to be so different from the animals around him. But it was still a story. It was not evidence. In short, it was sincere, but sheer, literature.” (p. 27)

“Literature” then, not science, Wolfe concludes — all the more so since evolutionary theory flunks all five commonly acknowledged tests for a valid scientific hypothesis:

Observability

Ability to be replicated

Capacity for Popperian falsification

Can scientists make predictions from it?

Does it illuminate other puzzling areas of science?

Wolfe remarks apropos of those five criteria: “In the case of Evolution… well…no…no…no…no… and no. In other words, there was no scientific way to test it.” (p. 27)

Ape and (Wo)man

In fact, Wolfe suggests with devastating bathos that what moved Darwin to postulate ape ancestry for humankind had nothing to do with science, but rather his visit to London Zoo in 1838 and his observations there of the facial and postural movements of the female orangutan, “Jenny,” sometimes sentimentally decked out in women’s clothing by her keepers.  Such were the rather skewed perceptions which informed Darwin’s Descent of Man (1871) and which, Wolfe reasons, will have lain behind the accumulated excesses and improbabilities of that much later, Darwin-inspired discipline which took off in the 1970s, calling itself first sociobiology before tactically rebranding itself evolutionary psychology.7

With the benefit of hindsight, it appears that the morphological link between ape and (wo)man becomes on closer inspection much less straightforward than it might at first appear, as is shown pre-eminently in the different language competences of apes and humans. To establish a convincing evolution of ape to human it would be necessary to establish that simians could over time have increased their communicative vocabularies so as to transform inarticulate emotional cries into specific vocal symbols. But this in turn brings up the closely related problem of how to explain the rapid mentalprocessing on which articulate speech depends. Without the simultaneous co-adaptation of the simian brain, how could the facility of speech, which depends on the interdependent agency of the brain in tandem with the specialised organs of vocal articulation, have developed by the essentially aleatory processes of natural selection? In order to prove that connection, one would have to be able to point to a precise physiological/neurological pathway of development, which nobody has yet been able to establish.8

Driving Darwin Crazy

How humankind gained its monopoly on language was a puzzle apt to drive Darwin crazy, writes Wolfe, and his co-discover Alfred Russel Wallace to one of the biggest U-turns in recorded history when he came to renounce his own theory of natural selection tout court.  By contrast, notes Wolfe, “a cosmogonist like Darwin couldn’t let it go at that. Speech had to have some animal genealogy…had to fit into his Theory of Everything.” Hence there emerged, concludes Wolfe, “Darwin’s real tour de force of literary imagination, the Descent of Man.” (p. 65) Here he had the licence to develop his Kipling-esque just-so stories (this allegation was made by the late Stephen Jay Gould, to the predictable displeasure of many colleagues). Darwin’s imaginative forays certainly ran counter to the more sober professional counsels of the day. The Philological Society of London in 1872 imposed a form of moratorium on research into language’s origin in 1872 and had been preceded by the Linguistic Society of Paris which actually banned speculation on this subject in 1866.

Bringing the story up to date, Wolfe points out that Noam Chomsky, who for decades thought that he had cracked the language problem by his postulation of a language “organ” situated in the brain, finally threw in the towel and admitted defeat. And as Wolfe somewhat impishly points out, if Chomsky, who had never accepted the development of language by successive evolutionary adaptations, and was now recanting his “organ” theory, then this inevitably had large implications: “Chomsky made it clear he was elevating linguistics to the altitude of Plato’s transcendent eternal universals… He was relocating the field [of inquiry] to Olympus.” (p. 89)

This meant in plain English that he was all but conceding language might have been “God-given” which, in Richard Lewontin’s old phrase, could be construed as the heresy of “allowing a divine foot in the door.”

The Zero-Sum Game

As Wolfe documents, a whole host of “certified geniuses” have failed to crack the human language problem, and this must count as a blow to Darwinian ideas of evolution. For Darwin’s theory is essentially a zero-sum game — if it fails to explain one of its aspects, it flunks the lot. For instance, if you do not prove that life originated by the chemical fluke of abiogenesis, then you cannot coherently argue that “natural selection” went to work on a “creation,” which you have not even proved to have occurred in the way you describe. The well-known Miller-Urey experiment in 1953, designed to spark life in a test tube, was not ultimately successful. Its implicit promise was to be able to extend Darwin’s timeline back to the pre-organic formation of the first cell of life, and so establish the fundamental point of departure for the mechanism of natural selection to go to work on. This would also of course have delivered a stunning victory for the materialist position. In the event, though, it succeeded only in dealing a disabling body blow to materialist notions by its failure to discredit the theistic position.

Without a traceable abiogenetic moment, Darwin’s entire theory of evolution via natural selection fails: as matters stand, the bare emergence of living cells remains an unsolved mystery, let alone the claimed corollary of that mysterious and suspiciously unexplained cellular “complexification” said to follow from it and to have occasioned in future time the fabled development from microbes to (wo)man. In fact, the most significant finding of Miller and Urey appears to have been a presumptive indication of a supra-natural etiology for the cellular system — an inference to theistic creation or theistic evolution which was of course the very obverse of the result both scientists were seeking. 

Hence the attempt to discuss the subject of how the process of selection by Nature began to operate whilst not even broaching the question of how Nature itself arose in the first place must count as a major evasion and as a failure of Darwinian theory as a whole. Which is why Wolfe concludes his study with remarks which call into question the whole neo-Darwinian narrative: “To say that animals evolved into man is like saying that Carrara marble evolved into Michelangelo’s David.” (p. 169) We should be grateful to Wolfe for his single foray into the area of evolutionary speculation, deserving, I would add, of the kind of readership numbers which he was able to command for his creative works.

References

The Novels of Thomas Love Peacock, edited by J. B. Priestley (London: Pan, 1967), p. xvix.

Wolfe, The Kingdom of Speech (London: Jonathan Cape, 2016).

The 20th century’s premier linguist, Noam Chomsky, never backed the idea of language being an evolutionary “adaptation” and latterly even forsook his own theory of there being a language “organ” in the brain. In later years Chomsky retreated to a position of stoic bafflement in the face of the inexplicable. See Wolfe, pp. 3-6. 

I am thinking for instance of the television cosmologist Hakeem Oluseyi (distinguished research professor at the Florida Institute of Technology) whose TV persona contrives not to take either himself or the theories of sundry colleagues overly seriously.

And of course it does come perilously close to the Genesis account, because according to the originating father of the Big Bang theory, the Catholic priest Georges Lemaître, the present exponential expansion of the universe could, by our reversing the process, be traced all the way back to the putative cosmic microdot, the primeval atom. 

See Max Jammer, Einstein and Religion: Physics and Theology (Princeton: Princeton UP, 1999), pp. 253-257.

Wolfe refers to Darwin’s own words in the peroration to his Origin of Species as a kind of “smoking gun” linking Darwin with sociobiology: “In the distant future I  see open fields for far more important researches. Psychology will be securely based on a new foundation, that of the necessary acquirement of each mental power of gradation. Light will be thrown on the origin of man and his history.” (p. 44)

The explanation Darwin advanced in The Descent of Man for his alleged perfectly orchestrated co-adaptation was entirely speculative, as for instance when he muses on where we humans might have got our superior IQ and articulacy from: “The mental powers of some earlier progenitor of man must have been more highly developed than in any existing ape, before even the most imperfect form of speech could have come into use; but we may confidently believe  that the continued use and advancement of this power would have reacted on the mind itself, by enabling and encouraging it to carry on long trains of thought.”

NEIL THOMAS

Neil Thomas is a Reader Emeritus in the University of Durham, England and a longtime member of the British Rationalist Association. He studied Classical Studies and European Languages at the universities of Oxford, Munich and Cardiff before taking up his post in the German section of the School of European Languages and Literatures at Durham University in 1976. There his teaching involved a broad spectrum of specialisms including Germanic philology, medieval literature, the literature and philosophy of the Enlightenment and modern German history and literature. He also taught modules on the propagandist use of the German language used both by the Nazis and by the functionaries of the old German Democratic Republic. He published over 40 articles in a number of refereed journals and a half dozen single-authored books, the last of which were Reading the Nibelungenlied (1995), Diu Crone and the Medieval Arthurian Cycle (2002) and Wirnt von Gravenberg's 'Wigalois'. Intertextuality and Interpretation (2005). He also edited a number of volumes including Myth and its Legacy in European Literature (1996) and German Studies at the Millennium (1999). He was the British Brach President of the International Arthurian Society (2002-5) and remains a member of a number of learned societies.

College outdated?

Exiting the cave?

 Paul Nelson: Freeing Minds Trapped in a Naturalistic Parabola

Evolution News @DiscoveryCSC

On a classic episode of ID the Future, philosopher of biology Paul Nelson talks with host Andrew McDiarmid about pursuing intelligent design theory in a science culture committed to naturalism. As Nelson puts it here, it’s about trying to communicate with scientists who are trapped in a “naturalistic parabola.” That parabola sets the rule and defines the boundaries for science: naturalistic answers only. And it extends to infinity, so no finite number of objections or counter-examples can force naturalistic scientists out of it. Nelson, however, offers an alternative strategy for drawing them out of the parabola. Download the podcast or listen to it here.

The thumb print of JEHOVAH re: Earth's giants.

 Prior Fitness and Dinosaurs

David Coppedge

How big can animals get on a given planet? Michael Denton has made a compelling case that given a habitable planet the size of Earth, humans must be the right size to have the ability to use fire and create technology (The Miracle of Man, pp. 194-197). Humans appear to have the optimal size for these purposes, with arm lengths and hand shapes appropriate for swinging axes and hauling wood for the controlled use of fire. 

These optima have allowed humans to develop modern technology. Physical laws, he shows, rule out the possibility that we could do all we do if we were as small as ants or as tall as 60-foot giants. “We could be neither fire makers nor metallurgists if we were significantly smaller” than we are, he says.

On the other hand, it is fortunate that the ability to hew wood and mine for ores does not necessitate kinetic forces much greater than those that can be generated by organisms of our dimensions. While significantly larger android beings could exert greater kinetic forces, the design of a bipedal primate of, say, twice our height would be severely constrained by kinetic and gravitational forces and be structurally problematic.

Why? For one, and as discussed in Chapter 9, mass (and weight) increases by the length cubed (L3) while the strength of bone and the power of muscles increases only by the length squared (L2). [Emphasis added.]

If we were giants, we would be at daily risk of shattering our bones into pieces. And that’s not all that physics requires of us. In addition to the right body size and shape, Denton argues that we must live on the right size planet. If Earth were smaller, ants might do fine, but such a planet could not maintain a life-giving atmosphere. If Earth were larger, gravity would “exacerbate the dangers of tripping” for upright bipedal creatures like us. Higher gravity would impose “severe constraints on the capacity of muscles to empower movement and support an upright bipedal stance.” Undoubtedly those constraints would impose ripple effects on all our systems: circulatory, respiratory, metabolic, and everything else.

Design Inference from Bones

What about size limits on big animals, like the giant sauropods? Given Earth’s gravity, are there physical limits to their existence, too? 

We don’t expect to find sauropod technology, but the same physical laws (mass increase with height) apply to them. The giant sauropods like Titanosaurus, Ultrasaurus, and Seismosaurus may have lived close to the physical limits of size on an Earthlike planet. Blue whales grow even more massive but are buoyed by water. Extant whales and large land mammals allow us to test theories about design limitations. What about giant creatures that can only be known from their bones?

Denton says that large land animals reduce the risk of falling (and breaking their bones) by walking on all fours. Even so, falling endangers horses and cows. A two-meter tall man faces 20 to 100 times the force of a fall compared to a two-foot child, he notes. (p. 196) The larger the animal, the greater the danger. The fact that giraffes and elephants can survive to adulthood suggests that their large bodies are well engineered for stability. From reconstructions of dinosaurs, the bipedal ones (like theropods) appeared to have good balance because of their tails, and the quadrupeds also had long tails and big feet for stability. In every case, engineering for stability would require attention to bone density, muscle strength, and kinesthetic sense (e.g., inner ear balance organs). 

Biological Cushions

Scientists at the University of Queensland in Australia applied engineering design principles to the largest land animals that ever lived: the sauropods. They applied what is known about tissue anatomy and physiology of elephants and other extant large animals. Elephants, despite appearing to walk flat-footed, actually walk on their toes. Their heels are cushioned by soft tissue padding made of muscles, tendons, ligaments, cartilage, and sole skin. This padding is a design requirement due to the elephant’s high mass. The Australian team wondered if dinosaurs also required foot pads.

Without having living sauropods available to observe, physiologists can infer things from the data available. Knowing that mass increases by the cube of length, biophysicists can estimate requirements for bone density and muscle strength for the giant dinosaurs. The fossilized bones, though mineralized, provide cross-checks for those inferences to a certain extent. Trackways also inform the diameters and shapes of dinosaur feet. What can’t be checked is the soft tissue padding around the foot bones, which is not preserved in fossils.

The Queensland team, led by Andréas Jannel, inferred that a sauropod would have needed padding in its feet to survive. And since dinosaur foot bones are not homologous to elephant feet, the padding had to be designed differently than the padding observed in the hind foot (pes) of an elephant or rhino. Their open-access paper in Science Advances explains how they inferred foot padding as a requirement.

Our results show that, irrespective of skeletal pedal posture (Fig. 1), all sauropodomorph specimens examined (i.e., representatives of distinct clades and diverse body sizes) would have been unable to support their weight without a soft tissue pad in the pes (Figs. 2 and 3). All skeletal morphotypes without a soft tissue pad resulted in maximum von Mises stresses higher than 500 MPa [megapascals] for all pedal models (up to 5000 MPa as recorded in Rhoetosaurus brownei; Fig. 3). As expected, bone stress increased principally in the shafts of each metatarsal and the most proximal phalanges (Figs. 2 and 3), likely due to the pedal posture, boundary conditions, and the fact that the metatarsals are the longest bones in the sauropod pes. Mechanically, it is highly unlikely that sauropod pedal bones could have withstood bone stresses of this magnitude without failing. This is because sauropod bones have been shown to retain the general structural properties of Haversian bone tissue seen in modern birds and large mammals, indicating that they were most likely subjected to comparable mechanical constraints. In humans and bovids, cortical bone (e.g., such as in the femur) has been evaluated to withstand maximum stress < 150 to 200 MPa (44, 45). Hence, within the context of comparable loading regimes, the mechanical state of each sauropod model examined suggests that all skeletal pedal postures would most likely have resulted in mechanical failure (e.g., stress fractures). This state would have been intensified when subjected to repetitive heavy loadings, as would be expected during normal locomotion, ultimately resulting in fatigue fracture in all digits. Being unable to support or move properly, the high probability of mechanical failure would have had a substantial impact on the animal’s survival.

Thinking Like Engineers 

The team used this reasoning to construct models showing where soft tissue would have been needed for cushioning the foot bones of various sauropod species. That’s thinking like engineers. These scientists, being Darwinists, believe that the engineering was supplied by natural selection. But that’s a story for another time. 

The fact remains that they made a design inference based on physics, fossils, and comparisons with living animals. As Denton argues in his “Privileged Species” books and videos, physical laws constrain what beings are possible on a habitable planet. That humans and other living beings thrive so well, and have thrived through Earth’s history, suggests that prior fitness was designed in the fabric of the earth and the universe. And if that is the case, then it’s not a big leap to reason that the specific forms these organisms took were also crafted according to engineering principles — with some artistry thrown in, too.

Darwinism continues to devolve.

 Mammoth Support for Devolution

Michael Behe

The more science progresses, the more hapless Darwin seems.

In my 2019 book Darwin Devolves I showed that random mutation and natural selection are powerful de-volutionary forces. That is, they quickly lead to the loss of genetic information. The reason is that, in many environmental circumstances, a species’s lot can be improved most quickly by breaking or blunting pre-existing genes. To get the point across, I used an analogy to a quick way to improve a car’s gas mileage — remove the hood, throw out the doors, get rid of any excess weight. That will help the car go further, but it also reduces the number of features of the car. And it sure doesn’t explain how any of those now-jettisoned parts got there in the first place.

The Bottom Line

The same goes for biology. Helpful mutations that arrive most quickly are very much more likely to degrade genetic features than to construct new ones. The featured illustration in Darwin Devolves was the polar bear, which has accumulated a number of beneficial mutations since it branched off from the brown bear a few hundred thousand years ago. Yet the large majority of those beneficial mutations were degradative — they broke or damaged pre-existing genes. For example, a gene involved in fur pigmentation was damaged, rendering the beast white — that helped; another gene involved in fat metabolism was degraded, allowing the animal to consume lots of seal blubber, its main food in the Arctic — that helped, too. Those mutations were good for the species in the moment — they did improve its chances of survival. But degradative mutations don’t explain how the functioning genes got there in the first place. Even worse, the relentless burning of genetic information to adapt to a changing environment will make a species evolutionarily brittle and more prone to extinction. The bottom line: Although random mutation and natural selection help a species adapt, Darwinian processes can’t account for the origins of sophisticated biological systems.

In Darwin Devolves, I also mentioned work on DNA extracted from frozen woolly mammoth carcasses that showcased devolution: “26 genes were shown to be seriously degraded, many of which (as with polar bear) were involved in fat metabolism, critical in the extremely cold environments that the mammoth roamed.” It turns out that was an underestimate. A new paper1 that has sequenced DNA from several more woolly mammoth remains says the true number is more than triple that — 87 genes broken compared to their elephant relatives. The authors write of the advantages provided by destroyed genes (references omitted for readability):

Gene losses as a consequence of indels and deletions can be adaptive and multiple case studies investigating the fate of such variants have uncovered associations between gene loss and mammalian phenotypes under positive selection. In laboratory selection experiments, gene loss is a frequent cause of adaptations to various environmental conditions. Given that we focused on those indels and large deletions that are fixed among woolly mammoths, the majority of these protein-altering variants likely conveyed adaptive effects and may have been under positive selection at some point during mammoth evolution. We did not find specific biological functions overrepresented among these genes (see methods), but many of the affected genes are related to known mammoth-specific phenotypes, such as total body-fat and fat distribution (EPM2A, RDH16, and SEC31B), fur growth and hair follicle shape and size (CD34, DROSHA, and TP63), skeletal morphology (CD44, ANO5, and HSPG2), ear morphology (ILDR1 and CHRD), and body temperature (CES2). In addition, we find several genes associated with body size (ZBTB20, CIZ1, and TTN), which might have been involved in the decreasing size of woolly mammoths during the late Pleistocene.

There’s Lots More

The point is that these gene losses aren’t side shows — they are the events that transformed an elephant into a mammoth, that adapted the animal to its changing environment. A job well done, yes, but now those genes are gone forever, unavailable to help with the next change of environment. Perhaps that contributed to eventual mammoth extinction.

As quoted above, the mammoth authors note that gene losses can be adaptive, and they cited a paper that I hadn’t seen before. I checked it out and it’s a wonderful laboratory evolution study of yeast.2 Helsen et al. (2020) used a collection of yeast strains in which one of each different gene in the genome had been knocked out. They grew the knockout yeast in a stressful environment and watched to see how the microbes evolved to handle it. Many of the yeast strains, with different genes initially knocked out, recovered, and some even surpassed the fitness of wild-type yeast under the circumstances. The authors emphasized the fact of the evolutionary recovery. However, they also clearly stated (but don’t seem to have noticed the importance of the fact) that all of the strains rebounded by breaking other genes, ones that had been intact at the beginning of the experiment. None built anything new, all of them devolved.

Well, Duh

That’s hardly a surprise. At least in retrospect, it’s easy to see that devolution must happen — for the simple reason that helpful degradative mutations are more plentiful than helpful constructive ones and thus arrive more quickly for natural selection to multiply. The more recent results recounted here just pile more evidence onto that gathered in Darwin Devolves showing Darwin’s mechanism is powerfully devolutionary. That simple realization neatly explains results ranging from the evolutionary behavior of yeast in a comfy modern laboratory, to the speciation of megafauna in raw nature millions of years ago, and almost certainly to everything in between.

References

Van der Valk, Tom, et al. 2022. Evolutionary consequences of genomic deletions and insertions in the woolly mammoth genome. iScience 25, 104826.

Helsen, J. et al. 2020. Gene loss predictably drives evolutionary adaptation. Molecular Biology and Evolution 37, 2989–3002.

Common descent v. Common design again.

 Why Their Separate Ancestry Model Is “Wildly Unrealistic”

Emily Reeves

In my post yesterday I outlined how Erika, aka the popular evolution YouTuber “Gutsick Gibbon,” critiqued my earlier post, which commented on an important paper in the field of phylogenetics, Baum et al. (2016), which purported to test separate ancestry. Between 7:55 and 9:24 of her response video, Erika shows a diagram (above) to respond to my point that the Baum et al. (2016) paper tested a model of separate ancestry that is not endorsed by anyone in the ID community.

Here’s what Erika, aka Gutsick Gibbon, is saying. In the diagram, she has two different models of what creationists (left) and intelligent design (ID) proponents (right) might be saying. (Note that she disagrees with both; she’s just trying to describe what she thinks the groups are saying.) Each “finger” in the diagram is supposed to represent an instance where the designer acted to influence the course of biological history. The left tree is supposed to show what she thinks the creationist’s model is that was tested by Baum et al. (2016). She mistakenly thinks that ID proponents are angry because we’re really putting forth some model like the diagram on the right — where a designer creates a group but then allows evolutionary tinkering. So, she thinks we’re upset because Baum et al. (2016) didn’t include tinkering in their model. This is actually not the case.

When I argued that Baum et al. (2016) failed to properly test separate ancestry, that has nothing to do with a failure to incorporate “tinkering” into the model. Also, as a side note, ID proponents do not advocate a “tinkering” hypothesis. This is a common misconception about the ID view. Instead, the primary objection of ID proponents to the Baum et al. (2016) paper is due to how the separate ancestry and family ancestry models were created in the first place. In short, Baum et al. (2016) assumes that shuffling of the synapomorphies is an accurate model for separate ancestry. ID proponents and others who have a design-based perspective would heartily reject that, for reasons I will explain.

How They Chose Data for the Separate Ancestry Model

Baum et al. (2016) uses several different datasets to test separate ancestry. Their molecular dataset, our focus here, is from a 2011 paper by Perelman et al. where 54 genes were used to construct a molecular phylogeny of living primates. (We’ll call this the “Perelman dataset.”) Primates all have around 30,000 genes, so the first question is how the authors got from 30,000 genes to 54. Note the details given from Perelman et al. (2011):

A complete list of 54 primer sets used in this study is presented in Table S2. This list includes primers from earlier studies (Murphy et al. 2001), as well as those designed specifically for this study using a unique bioinformatics approach (Pontius, unpublished data). (Perelman et al. 2011)

If you look at Table S2 in you can see that the majority (38 of the 54 genes) came either from Murphy et al. (2001) (9 genes) or were specially designed for the study and no details are given (29 genes). For our purpose, let’s just look at the 9 taken from Murphy et al. (2001) which are described as being selected in the following way:

The GenBank and UniGene databases (NCBI) were searched for genes with exons of sufficient length (>200 bp) and variability (80±95% nucleotide identity between mouse and human), thereby providing adequate variation for the purpose of phylogenetic and somatic cell/ radiation hybrid mapping. (Murphy et al. 2001)

What’s Happening Here? 

Two types of selection or filtering are going on when they choose genes for their study. The first selection is to remove genes not present in all the species they were studying. In other words the genes had to be within the databases, be of sufficient size, and exist in all the species being considered. This rules out species-specific genes such as orphan genes. The second selection is that genes having the greatest number of phylogenetically informative sites or synapomorphies were chosen. (A synapomorphy is a variant/trait that is shared by at least two descendent taxa and thought to be inherited from a most recent common ancestor, where it evolved.) In order to win at this second selection, a gene should have the greatest number of variants which differ between at least two taxa, but in the same way (i.e., at site 1 two taxa have ‘A’s while the ancestral site was a ‘G’). A simpler way of putting this is they picked genes that varied the most between species, but in a likely functional way. If you look at Table 1 from Murphy et al (2001) you can see that the ADORA3 gene has 191 phylogenetically informative sites out of 330 base pairs. That means that at 191 positions it differs between at least two of the comparison taxa in a consistent way. To help better understand why these filters are stacking the deck from a design perspective, I want to give an analogy.

Let’s do a thought experiment where we want to create a distance tree demonstrating the evolution of household chairs. We choose five traits to compare. Those five traits must be exhibited by all the chairs and the five traits must vary between at least two chairs. This type of selection effectively eliminates unique properties of the chairs such as leather because not all chairs have this. Instead it prioritizes specific parts of chairs that were made intentionally different for functional or economic reasons. This type of selection on a designed object, such as a chair, will create an intuitive hierarchical tree even though the chairs are not actually related. How? Read on.

For example, screws, which hold chairs together, are likely to be a trait shared by all chairs (first criterion passed), but screws aren’t likely to vary a lot between chairs and therefore wouldn’t be selected as a trait. On the other hand, legs are a trait shared by all chairs and these are likely to vary quite a bit between different chairs based on the function of the chair. Children’s chairs will have shorter legs. Decorative chairs will have aesthetically pleasing legs. Folding chairs will have collapsible legs. Some chairs may have four legs while others five or even more. Seats are another example of a trait that will be common to all but differ a lot. Children’s seats on chairs will be smaller. Decorative chairs will have aesthetically pleasing seats. Collapsible chairs will have mobile seats. Thus, a selection for “differentness” with designed objects enriches for traits that cluster due to functional constraints or compatibility, not ancestry. If organisms are in fact designed, a very similar phenomena could be occurring in these phylogenetic comparisons.

Now let’s look at how this data set was used by Baum et al. (2016) in their separate ancestry model and what about the model is so problematic from an ID perspective.

They Used Synapomorphy Shuffling to Test Separate Ancestry

In describing the separate ancestry model Baum et al. (2016) says:

A key feature of the species SA [separate ancestry] model is that for each character [meaning genetic variants or fossil characters] the state drawn by each species is independent of that drawn by other species.

But what do they mean by saying that the state drawn by each species is “independent” of that drawn by another species? How are they actually creating their separate ancestry model? What I’ve gathered is this essentially means that in their “separate ancestry” model, the traits or synapomorphies were shuffled randomly to create a hypothetical model of what they think separate ancestry would be. I will illustrate with an example in Figure 1 adapted from the molecular Perelman dataset, where I took actual names of genes used by Baum et al. (2016), but then represented the different synapomorphies of those genes as spelling changes for the function of the gene.

To elaborate, in Figure 1 above are genes ABCA1, BNDF, AFF2, APP, and ATXN7. I have represented their DNA sequences simply as lowercase letters (transport, memory, splicing, migration, and cytoskeleton respectively) corresponding to their major functions. Then, to represent the synapomorphies between these organisms I’ve introduced some spelling errors. For example, in Figure 1A the ABCA1 gene in organism 1 is the sequence is transwort (lowercase) and BNDF is menory, AFF2 is splycing, APP is megration, and ATXN7 is cytosqeleton respectively. The pattern of changes within the gene (columns) are the same for all five genes in Figure 1A — notice how top to bottom the phylogenetic trees are the same. Thus, Figure 1A represents the data observed with one important caveat — I have artificially made the pattern of synapomorphies perfect (CI =1) just for clarity (not the case in the real data).

Now, the authors Baum et al. (2016) constructed their separate ancestry model by permuting (shuffling) the synapomorphies of these sequences (Figure 1B), in a random manner which assumed there would be no reason to find correlations of traits across different organisms. Here’s how they described their methods:

To evaluate whether the observed hierarchical signal is more than expected under species of family SA, we used the PTP test which uses a Monte Carlo approach to simulate data under the SA hypothesis. We implemented PTP tests using the permute function of PAUP* ver. 4.0a134-146 with parsimony as optimality criterion and hence tree length as a measure of tree-like structure.

In other words, Baum et al. (2016) gave the synapomorphy of the ABCA1 gene sequence of organism 2 to organism 4 and vice versa using a permute function (see Figure 1B). They did not just swap the whole genome sequence between two organisms but swapped individual characters — in this case base pairs — to remove the connection between them (notice how top to bottom the colors are scrambled). As expected, after random shuffling of the synapomorphies the tree length drastically increased — meaning more evolutionary events were required to explain the data, and the tree was not very parsimonious (see Table 1 from Baum et al. (2016)).

Following this they calculated the p-values (see Table 3 from Baum et al. (2016)). The p-values are outrageously low, dictating a strong rejection of the separate ancestry model tested. Erika interprets this here as indicating that at least this model of separate ancestry is a totally unreasonable hypothesis. Their method is given below:

For many of the tests the observed test statistic fell well outside the range of values obtained under the SA hypothesis. In such cases, we report the distance of the observed data from the mean of the SA distribution in units of the SD (the z-score) and also provide a P-value assuming a normal distribution. Although the latter is only an approximation, it will provide the reader with a sense of how improbable the data would be under SA. 

Of course, I reject this model of “separate ancestry” as well. This model, as they’ve developed it, is totally unrealistic for all kinds of reasons and therefore far less likely than the observed model. Now, anytime one observes this type of data in biology it should definitely make one question if not immediately reject the model. Erika also partially recognizes this because in reference to these zeros she also says “That’s insane! You don’t see that in regular science.” Basically, p-values this low typically indicate that there is something really wrong with one’s model. So, let’s talk about this, and what might be wrong with their model of separate ancestry.

Synapomorphy Shuffling is Not a Good Test of Separate Ancestry

The short(er) explanation for why synapomorphy shuffling is not a good model of separate ancestry is that synapomorphies or traits may cluster for designed systems based upon functional reasons like optimization, constraints, or compatibility. Recall that a synapomorphy is a trait or site uniquely shared by members of a group that helps to define that group. Under typical phylogenetic thinking, synapomorphies are thought to exist because they evolved in the common ancestor that gave rise to the group. But in an ID-based world, synapomorphies might exist because they represent a suite of traits required for a group of organisms to perform some important function related to their survival. 

In designed systems, traits don’t vary randomly, and often vary according to predictable patterns which may be related to functional needs. In biology, these functional needs could be related to an organism’s niche, lifestyle, locomotion, metabolism, diet, or other behaviors. In other words, organisms which live in similar niches and/or have similar lifestyles, modes of locomotion, metabolisms, diets, or other behaviors, may tend to have similar traits all related to functional constraints that are required for that organism to survive in its environment. Thus, in a designed biosphere, traits won’t vary randomly but will follow similar patterns, correlations, and relationships across organisms according to their various survival needs. To put it simply, organisms with similar lifestyles will show similar architecture. This will be true not because of common ancestry but because of design constraints which must be fulfilled for an organism to survive in its environment. 

Now, the Long(er) Answer… 

ID proponents have a problem with this model of separate ancestry because it does not account for anticipated taxa-specific design constraints (aka what I am calling “functional synapomorphies”). Most ID proponents would hold that only synapomorphies that are historical in nature could be shuffled in such a fashion. As a thought experiment, if one selected synapomorphic chair traits, a very nice nested hierarchical pattern will result. Collapsible chairs will cluster, desk chairs will cluster, armchairs will cluster, children’s chairs will cluster, and the universal common ancestor might be something like a stool. Thus, if a synapomorphy is functional (i.e., contributes to the function) and not historical, this random shuffling of synapomorphies would be analogous to taking chair-specific design differences (like a collapsible seat and short legs for a children’s chair), mixing them up, and then observing that collapsible chairs and children’s chairs no longer group together. When you shuffle functional traits of designed objects, you will get statistical zeros, because you have obliterated the design signal. Most likely you’d also get some quite weird designs that don’t work very well! Imagine outdoor patio furniture with traits of indoor office chairs. It wouldn’t work!

Given how the data were selected in the first place, it is very likely that many of these synapomorphies are functional.

The reason why functional synapomorphies cannot be used is because hierarchical clustering of functional synapomorphies or traits are abundant in scenarios that we know have not arisen due to a process of descent with modification. Don’t like my chair analogy? Take the distance tree, created by Doolittle and Bapteste 2007, of French departments based on the number of shared sur-names (See Figure 1b in the paper). This is a great example of how functional synapomorphies or traits can result in logical clustering of data when no descent with modification process has occurred. Baum et al. (2016)’s error is therefore as follows: They assume that design must produce random distributions of traits. However, all of our experience with sets of designed systems shows this is not the case. Erika doesn’t appreciate this point, and thus she misunderstands our critique of the Baum et al. paper.

What we know about design, from engineering and other life scenarios, is that design often creates a hierarchical similarity pattern centered around function that could look like ancestry if one forces it. Why do designers produce these hierarchical patterns? They aren’t trying to be deceptive, mimicking systems that look like they are the product of common ancestry. Rather, designers are simply applying logical design considerations like optimization, constraints, compatibility, dependencies, or reuse during the design process.

Thus, I hold that the model of separate ancestry rejected in the Baum et al. (2016) paper is not endorsed by most in the ID community because it does not account for the design expectation that functional synapomorphies or traits will cluster due to optimization, constraints, and a need for compatibility.

On Monday, I will look at the consistency of the phylogenetically informative sites for the Baum et al. (2016) paper. Spoiler alert: It looks like design.

Yet more on the struggle for the "empire of God"

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Primeval tech of the "lowly" sponge

 Complex Specified Information in the Lowly Sponge

David Coppedge

Sponges are outliers in biology’s big bang, the Cambrian explosion. Their embryos appear in Precambrian strata, leading some to consider them primitive. That’s an illusion. New studies of how they construct their skeletons with silica “spicules” have revealed design principles remarkable enough to inspire biomimicry. 

The punch line first — here’s how a news item from Current Biology concludes:

“This work not only sheds new light on skeleton formation of animals, but also might inspire interdisciplinary studies in fields such as theoretical biology, bioengineering, robotics, and architectural engineering, utilizing mechanisms of self-constructing architectures that self-adjust to their environments, including remote environments such as the deep sea or space,” the researchers write. [Emphasis added.]

Goodness! What are these simple animals doing to arouse such commotion? Just watch the video clip in the article of sponge cells at work. Then, look at the Graphical Abstract in the source paper and see the steps diagrammed in well-organized stages: (1) spicules are manufactured in specialized cells, then transported to the construction site; (2) the silica spicules pierce the epithelial tissue; (3) they are then raised up into position; (4) the bases are cemented by collagen provided by basal epithelial cells.

This simple animal knows, in short, how to build a house with pole-and-beam architecture in a way that self-adjusts to its environment.

That’s Pretty Impressive

Sponge skeletons, with their unique spicules, have been studied for a long time, but the manner of construction has been a mystery till now. What’s new, according to the Japanese researchers, is the identification of specialized “transport cells” that carry and finally push the spicules through the epithelia, and cementer cells that fasten them in place like poles. The process reveals division of labor and an overall plan.

Here we report a newly discovered mode of skeleton formation: assembly of sponges’ mineralized skeletal elements (spicules) in locations distant from where they were produced. Although it was known that internal skeletons of sponges consist of spicules assembled into large pole-and-beam structures with a variety of morphologies, the spicule assembly process (i.e., how spicules become held up and connected basically in staggered tandem) and what types of cells act in this process remained unexplored. Here we found that mature spicules are dynamically transported from where they were produced and then pierce through outer epithelia, and their basal ends become fixed to substrate or connected with such fixed spicules. Newly discovered “transport cells” mediate spicule movement and the “pierce” step, and collagen-secreting basal-epithelial cells fix spicules to the substratum, suggesting that the processes of spiculous skeleton construction are mediated separately by specialized cells. Division of labor by manufacturer, transporter, and cementer cells, and iteration of the sequential mechanical reactions of “transport,” “pierce,” “raise up,” and “cementation,” allows construction of the spiculous skeleton spicule by spicule as a self-organized biological structure, with the great plasticity in size and shape required for indeterminate growth, and generating the great morphological diversity of individual sponges.

Inspiring Architects

This method of skeleton construction differs greatly from arthropods and vertebrates. It doesn’t appear to follow a set of rules or a preordained pattern, but it is very effective for sponges, “whose growth is plastic (i.e. largely depends on their microenvironment) and indeterminate, with great morphological variations among individuals.” Nevertheless, design and coordination is evident in the division of labor, the specialization of cells, and the end result that is good enough to inspire architects. If it were so simple, the authors would not have left many questions unanswered:

Many precise cellular and molecular mechanisms still remain to be elucidated, such as how transport cells can carry spicules, or how one end of pierced spicules is raised up. Additionally, one of the further questions that need to be answered is how sponges fine-tune their skeleton construction according to conditions of their microenvironment, such as water flow or stiffness of the substratum, since it is reported that the growth form of marine sponges changes according to the water movement of their environment.

Design is also evident in the self-organizational principles encoded in sponge DNA that make these results successful. Human intelligent designers would like to benefit from this knowledge. The authors conclude, repeating the “punch line”:

Intriguingly, our study revealed that the spiculous skeleton of sponges is a self-organized biological structure constructed by collective behaviors of individual cells. A chain of simple and mechanical reactions, “transport-pierce (by transport cells)-raise up (by yet unknown cells and/or mechanisms)-cementation (using collagenous matrix secreted by basopinacocytes and possibly by spicule-coating cells),” adds a spicule to the skeleton, and as a result of the iteration of these sequential behaviors of cells, the spiculous skeleton expands. As far as we know, this is the first report of collective behaviors of individual cells building a self-organized biological structure using non-cellular materials, like the collective behaviors of individual termites building mounds. Thus, our work not only sheds new light on skeleton formation in animals but also might inspire interdisciplinary studies in fields such as theoretical biology, bioengineering, robotics, and architectural engineering, utilizing mechanisms of self-constructing architectures that self-adjust to their environments, including remote environments such as the deep sea or space.

The reference to termite mounds is apt. The journal Science has described how these mounds, built by hundreds of individual termites, are able to “breathe” like an “external lung”:

Here’s how it works: Inside the hill is a large central chimney connected to a system of conduits located in the mound’s thin, flutelike buttresses. During the day, the air in the thin buttresses warms more quickly than the air in the insulated chimney. As a result, the warm air rises, whereas the cooler, chimney air sinks — creating a closed convection cell that drives circulation, not external pressure from wind as had been hypothesized. At night, however, the ventilation system reverses, as the air in the buttresses cools quickly, falling to a temperature below that of the central chimney. The reversal in air flow, in turn, expels the carbon dioxide-rich air — a result of the termites’ metabolism — that builds up in the subterranean nest over the course of the day, the researchers report online this week in the Proceedings of the National Academy of Sciences.

We know that some caves “breathe” as the temperature changes, but this is different. Termites construct their mounds for a purpose: to control the temperature and remove carbon dioxide for their health. It’s a bit like active transport in cells that draws in what the cell needs and removes what it doesn’t need, using machines that work against natural concentration gradients.

Intelligent Self-Organization

We all know that some beautiful things can self-organize without programming (snowflakes are a prime example). What we see here, though, are systems working from genetic programs for a purpose. In the case of sponges, its specialized cells cooperate in a plan to build a skeleton that adapts to the environment. In the case of termites, each individual insect’s genetic program makes it behave in a cooperative enterprise to build an air-conditioned mound. Such things do not arise by unguided natural forces. 

If functional self-organization were simple, why did five European countries take years “working to design the European Union’s first autonomously deployed space and terrestrial habitat”? The effort, called the “Self-deployable Habitat for Extreme Environments” (SHEE) project, has a goal of programming elements for “autonomous construction” of housing for astronauts on Mars or other hostile locales. It took years of work in design, prototyping, construction, and optimization to get these buildings to “self-deploy” with no humans in the loop.

So when a sponge can do it, we should see intelligent design behind the scenes — not the sponge’s intelligence, which admittedly is minuscule, but intelligence as a cause for the genetic information that allows the sponge to run a program that leads to a functional result. 

Those of us who appreciate the spectacular genetic programs that built the Cambrian animals should take note of the level of complex specified information in the lowly sponge. We can also notice that the sponge’s mode of construction bears no evolutionary ancestral relationship with the diverse, complex body plans that exploded into existence in the Cambrian strata. Sponges did well. They’re still with us. 

This article was originally published in 2015.

Emperor Darwin's new clothes?

 Darwin, Group Think, and Confirmation Bias

Neil Thomas

Yesterday I wrote about Charles Darwin and the British secularist tradition. The latter is the subject of a great volume of material discovered by Timothy Larsen, author of Crisis of Doubt: Honest Faith in Nineteenth-Century England. Larsen’s book provides a clue (as I read matters) that might be used to resolve what I in the company of many others find to be one of the greatest historical cruxes of 19th-century history. I refer here to the matter of how Darwinian theory, despite its lack of empirical support or even semblance of verisimilitude, was able to advance to its present position of orthodoxy. Since I suspect that the answer to this conundrum is most likely to be found in the area of group psychology, I would beg leave to make a small detour here to consider the issue of what we now term “confirmation bias” as that theme was treated by one of history’s most perceptive analysts of human nature, William Shakespeare.

Those acquainted with his drama Othello will know that Shakespeare’s psychological insight is nowhere more apparent than in his depiction of the negative dynamic between the eponymous hero and his villainous lieutenant, Iago. Although the exact motivation(s) behind Iago’s resentment of his military superior still remain a matter of critical debate, the reason for Othello’s unfounded jealousy of Michael Cassio for supposedly having committed adultery with Othello’s wife, Desdemona, is all too clear. Much in the play is made to hinge on the notorious prop of Desdemona’s handkerchief which Iago had contrived to misappropriate and plant in Cassio’s rooms and which Othello is duped into taking as “ocular proof” of Desdemona’s adultery. Iago’s malign stratagem works perfectly. As he had predicted, his chosen mark proved to be “as easily led by the nose as asses are.” Othello, witnessing the handkerchief, tragically succumbs to his own paranoid insecurities, and jumps to the wholly erroneous conclusion that his wife must be an adulteress with the colorful ladies’ man Cassio. Iago, in what is surely a particularly spot-on description of such confirmation bias, soliloquizes in an aside audible only to the audience,

I will in Cassio’s lodging lose this napkin

And let him [Othello] find it. Trifles light as air 

Are to the jealous confirmations strong

As proofs of holy writ. 

OTHELLO, ACT 3, SCENE TWO, LINES 373-6

“Trifles light as air/Are to the jealous confirmations strong/as proofs of holy writ”: in other words, once some particular thought, however poorly substantiated, has for whatever reason become lodged in our minds, it tends to develop into a Freudian idée fixe and all our future perceptions are somehow made to be congruent with that original idea. It is precisely for that reason in modern jurisprudence any information leading towards possible confirmation bias must be withheld from a jury to prevent it from jumping to conclusions.

Othello’s sexual insecurities were to have, mutatis mutandis, something of a 19th-century correlative in the insecurities and loss of nerve in matters of faith which were developing in a significant number of Victoria’s subjects in the first half of that century. All this was of course well before publication of the Origin, so that Darwin’s magnum opus will have served only to confirm and strengthen their mood of skepticism in a way comparable to that in which Desdemona’s handkerchief served to convince her husband (wrongly) of her infidelity. The empirically demonstrable truth-value of the Origin might have been negligible (in Shakespearean terms, a “trifle light as air”) but that mattered not a jot to persons already primed by their prior ideological formation to accept Darwin’s argument as a form of secular gospel. The Origin will have come together with their prior misgivings to create a “resultant of forces” precipitating an even greater degree of secularist thinking in many who had in any case all but bidden adieu to the religion of their youth. There is, however, some firm historical evidence that some of the more self-critical secularists were to experience a light-bulb moment in later life which prompted them to reassess their previous stance.

Reconversions

The secularists chosen for study by Larsen all eventually returned either to the faith they had initially rejected or to some other form of spiritual orientation. Typically, they would find over time that secularism offered no positive program for people to live by. Gordon came to refer to secularism as “just what you like-ism” which he took to be a recipe for immoral self-indulgence. William Hone came to realize that materialism could not account for the totality of human experience — there must be a power behind matter. There was a general feeling amongst the reconverts that their erstwhile skepticism might have been the result of “a procrustean system of logic, an oppressively narrow definition of reason. They came to believe that human beings knew more than could be proven by such a method.”1 Notably, the reconverts were also prompted by dint of lived experience and maturer reflection to revisit what seems to have been a very basic unexamined assumption amongst their number with the result that they now at long last “reassessed their assumption that the cause of radical politics and the working classes naturally led to an opposition to Christianity.”2

Not all returned to orthodox Christian forms of worship. Some “were led away from materialism by reengaging with the realm of spirit in a form decoupled from Christianity.”3 In this they made common cause with other, more famous secularists of the age such as Annie Besant, Charles Bradlaugh’s close ally, who went as far as crossing the floor from secularism to Madame Blavatsky’s theosophy. One may also think of Sir Arthur Conan Doyle whose hero, Sherlock Holmes, was the very apotheosis of dry secularism but whose author, although he had lost his faith in earlier years, was eventually to turn to spiritualism. Or in more recent memory there is the example of that later scion of the Huxley dynasty, Aldous, who turned in later years from a form of positivist philosophy to embrace Eastern mysticism and the so-called perennial philosophy.4

In a more minor key we can trace a comparable development in the rise in popularity of the English ghost story in the second half of the 19th century. This may in good part be understood as an imaginative protest against the growing desacralization of the world brought about by the burgeoning age of science. As Julia Briggs pointed out, the ghost story was in a superficial sense designed to scare readers but at a profounder level it supplied them with the comfort of a deeper spiritual reassurance:

For it [the ghost story] seemed at the outset to invite the reader’s modern cynicism, only to vanquish it with a reassertion of older and more spiritual values. Even amongst its superficial terrors it might provide subtle reassurances.5

Larsen, dissociating himself from the kind of “God’s funeral” historiography practiced by such writers such as Basil Willey, A. O. J. Cockshut, and A. N. Wilson,6 interprets such reversions as symbolizing a victory of the spiritual over the exclusively material worldview and goes so far as to claim that the reconverts “serve to orientate us toward the intellectual strength of the Christian tradition in nineteenth century tradition.”7 Whether such a large historical revision is warranted by the statistically limited sample of persons he adduces in his book may be open to question. What is not in question, however, is the service he has rendered in going beyond the top-down historiography practiced by many other historians of ideas. Instead, he has revealed a largely unsuspected but quite sizeable demographic of self-educated people who, although they were far distant from the major levers and megaphones of power, exerted a considerable influence in shaping ordinary people’s attitudes to fundamental existential issues. 

This finding is particularly significant since it throws light on the major historical crux mentioned above relating to how Darwin was able to “palm off” an empirically unattested theory on so many of his countrymen and women. We already know from Ellegård’s classic study of British press reactions to Darwin in the latter half of the 19th century that some sections of society simply resisted and disbelieved Darwin.8 Larsen’s researches, on the other hand, indicate that Darwin had a more forgiving and considerably less critical constituency of honest doubters and militant secularists to rely on. For that group Darwin’s work came to confirm what they had either already been persuaded of or else begun to figure out for themselves on other grounds. They were willing to give his theory a pass because it suggested an atheistic conclusion they had already arrived at by an alternative route. It was not Darwinism that they endorsed so much as the ideological direction in which his Origin of Species was thought to point, and so, like Thomas Huxley, they were more than willing to give Darwin their enthusiastic support.

packaging

One final, seemingly superficial but in practice rather significant point to be made in the matter of Darwin’s appeal to the secularist demographic is that his Origin will have made agreeable and accessible reading for this group of politically but not biologically informed individuals.9 It is attractively presented in a volume free of scientific jargon, and has often been lauded as the last specialist work fully intelligible to the man or woman in the street. It also comes laced with just the right amount of gentlemanly hesitancy to endear it to a British audience which might have been deterred by a showier or overly “intellectual” mode of presentation. Surely few other writers would have been minded to flag up their reservations about their own material in the same manner as Darwin who remarkably devoted a small chapter to “Difficulties on (sic) the Theory.”

By implicitly disclaiming airs of omniscience, Darwin avoided the vice most disliked by English readers: that of trying to appear “too clever.”10 As one 20th-century intellectual historian observed apropos of this strange national quirk, “People were as delighted with Darwin’s apparent lack of cleverness in youth as they were in 1940 with Mr. Churchill’s inability to learn Latin verbs at Harrow.”11 In reality, as we know, Darwin’s claims to discovery were every bit as trenchant as the literary detections shortly to be achieved by the abrasive fictional figure of Sherlock Holmes. However, to continue the Conan Doyle analogy, Darwin’s method of “packaging” those claims seemed more like an adumbration of the self-effacing manner later to be adopted by Holmes’s fictional foil, Dr. Watson. His readers will doubtless have concluded that the author of the Origin must surely be a regular sort of guy — “one of us” deep down despite his being, from their perspective, a toff. 

References

Larsen, Crisis of Doubt, p. 242.

Larsen, Crisis of Doubt, p. 243.

Larsen, Crisis of Doubt, p. 242.

Aldous Huxley, The Perennial Philosophy [1944] (New York: HarperCollins, 2009) contains a valuable later essay written by Huxley in the 1950s (Appendix, pp. 6-22) with an account of a spiritual odyssey not dissimilar to that of some of the “reconverts” considered above.

Julia Briggs, Night Visitors: The Rise and Fall of the English Ghost Story (London: Faber and Faber, 1977), p. 17.

Basil Willey, More Nineteenth-Century Studies: A Group of Honest Doubters (London: Chatto and Windus, 1963). A. O. J. Cockshut, The Unbelievers: English Agnostic Thought 1840-1890 (London: Collins, 1964); A. N Wilson, God’s Funeral (London: John Murray, 1999).

Larsen, Crisis of Doubt, p. 253.

Alvar Ellegård, Darwin and the General Reader: The Reception of Darwin’s Theory of Evolution in the British Periodical Press 1859-72[1958] (repr. Chicago: Chicago UP, 1990).

People in all ages have recognized how important it is for a writer to win the good will of his or her audience. Medieval rhetoricians had a ready formulation of this PR tactic in the term captatio benevolentiae (getting one’s readers on side).

Darwin’s diffidence was real enough, as is evidenced in the no fewer than five emended editions of the Origin which followed in quick succession in the decade following the first edition of 1859 in which he was able to interpolate his responses to critical objections to his work.

A. O. J. Cockshut, The Unbelievers, p. 176.

Finetuning: Multiple dice or a singular intellect?

 Generic Intelligent Design, the Multiverse, or One God?

Evolution News @DiscoveryCSC

On a new episode of ID the Future, Stephen Meyer takes a close look at the case not only for intelligent design, but also for a designer of the cosmos who is immaterial, eternal, transcendent, and involved. Meyer draws on evidence for design at the origin of life, in the origin of plants and animals, and from the fine-tuning of the laws and constants of chemistry and the initial conditions of the universe. He connects all this to the scientific evidence that the universe is not eternal but had a beginning — the Big Bang.

What about the main materialistic alternative for explaining this suite of evidence — the idea that there is a multiverse with our universe just being one of the lucky universes with just the right conditions to allow for advanced life? In step-by-step fashion, Meyer examines the multiverse theory and why it fails to explain away the insistent evidence of a cosmic designer. Download the podcast or listen to it here.