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Saturday 8 July 2017

Interview with a titan.

The political center is dead and gerrymandering killed it?:Pros and cons.

More fossils mean more doubt?

In Resolving Darwin's Doubt, New Cambrian Animal Fossils Are No Help at All


 

More complexity in the earliest multicellular animals intensifies what Discovery Institute's Stephen Meyer calls "Darwin's Doubt."

Euarthropods
A paper in Current Biology comes closest to demonstrating "the deep homology between exoskeletal features in an evolutionary continuum of taxa with distinct types of body organization." Author Javier Ortega-Hernández takes on "the euarthropod head problem" by finding similarities between two specimens from the Burgess Shale (Middle Cambrian). His analysis, though, only compares positions of complex tissues, not how they originated. Amid various controversies, he focuses on a relatively simple structure, the anterior sclerite (a front plate of cuticle) within one phylum, the true arthropods.

Despite its ubiquitous nature, the significance of the anterior sclerite remains controversial, as there is little agreement on the correspondence of this structure among stem- and crown-group euarthropods. [Emphasis added.]
His attempt at finding phylogenetic relationships, given such a trifling structure in a narrow range of animals, is less than convincing. Worse, he ignores the weightier matters of the explosive origin of the complex body plans of these animals.
Collinsium
Science media are excited about a new "spiky monster worm" from China, named Collinsium ciliosum (pictured above; original paper is in PNAS). If this is supposedly an ancestor of modern velvet worms, as researchers at the University of Cambridge claim, it was already complex, with spikes, a mouth with teeth, antennae, and filter feeding appendages. Its 72 spikes in rows down its back are particularly noteworthy. If anything, it looks more complex than "Today's 180 or so species of velvet worms [that] all look and act pretty much the same" (Science Magazine). "This isn't the first time that an ancestral group has displayed more diversity than its modern-day relatives," Live Science comments. If this is evolution, it's going backwards.

The critter is one of the first known animals on Earth to develop protective armor and to sport specialized limbs that likely helped it catch food, the researchers said. This newfound species lived during the Cambrian explosion, a time of rapid evolutionary development, they said.
Abrupt appearance? Rapid development? How this helps the evolutionary story is not clear. The Cambridge news item offers word salad as a distraction from the issues raised in Meyer's book Darwin's Doubt, which they simply ignore.

"Animals during the Cambrian were incredibly diverse, with lots of interesting behaviours and modes of living," said Ortega-Hernández. "The Chinese Collins' Monster was one of these evolutionary 'experiments' -- one which ultimately failed as they have no living direct ancestors -- but it's amazing to see how specialised many animals were hundreds of millions of years ago. At its core, the study of the fossil record seeks answers about the evolution of life on Earth that can only be found in deep time. All the major biological events responsible for shaping the world we inhabit, such as the origin of life, the early diversification of animals, or the establishment of the modern biosphere, are intimately linked to the complex geological history of our planet."
Anomalocaris
DebatingDDsmall.jpegStar of the Illustra documentary Darwin's Dilemma, the apex predator Anomalocaris was mentioned recently in connection with a new member of its family. This one, a giant named Aegirocassis benmoulae, was found in Morocco, indicating the global extent of the anomalocaridids. Unlike its more famous relative, "this anomalocaridid from the Ordovician exposes a second set of body flaps and reopens the question of how the two branches of arthropod legs evolved," Gregory Edgecombe notes in Current Biology. The authors of the paper in Nature are not much help to Darwin, having to invoke "convergent evolution" again:

Among arthropods, the size of A. benmoulae (over 2 m in length) is paralleled only by some pterygotid eurypterids and terrestrial arthropleurids. The evolution of gigantic filter-feeders within clades of nektic macrophagous predators is well documented in Mesozoic pachycormid fish and Cenozoic sharks and whales. The huge size of A. benmoulae represents a much earlier example of a filter-feeding lifestyle correlating to gigantism. The abundance of gigantic anomalocaridid filter-feeders in the high palaeolatitude Fezouata Biota points to a complex planktic ecosystem. Early Cambrian anomalocaridid filter-feeders also fed on zooplankton, but they remained relatively small. Although the Cambrian Explosion saw the establishment of the first complex planktic ecosystems, the convergent (Supplementary Text) rise of giant filter-feeding anomalocaridids during the Ordovician followed an increase in the abundance and diversity of phytoplankton and a consequent zooplankton radiation as part of the Great Ordovician Biodiversification Event.
Once again: abrupt appearance of complex body plans, complex ecosystems, and convergent evolution. None of this helps the evolutionary story or answers the key issue: where did the genetic information come from to build complex body plans with hierarchical structures and functional organs composed of new tissues and cell types?
Hallucigenia
When Hallucigenia was first found in the Burgess Shale a century ago, paleontologists couldn't tell top from bottom or front from back. The bizarre creature with paired spines pointing away from its paired legs was missing an important part: its head. Now, the head has been found. It's complex, with a pair of eyes and rows of teeth. This requires explaining more cell types and tissue types than before, exacerbating the problem Stephen Meyer identified in his book.
Martin R. Smith from Cambridge, with Jean-Bernard Caron from the Toronto Museum of Natural History, announced the discovery in Nature. Other sites, like PhysOrg and New Scientist, picked up the story and showcased the new artwork. For BBC News, Smith described his initial reaction:

By delicately chipping away at the rock, scientists found a spoon-shaped head with some surprising features.
"When we put it into the electron microscope, we were delighted to see not just a tiny pair of eyes looking back at us, but also beneath them a really cheeky semi-circular smile.
"It was as if the fossil was grinning at us at the secrets it had been hiding," explained Dr Smith.
Inside the creature's mouth, the researchers found a ring of teeth and then another set of teeth running from its throat down towards its stomach.
Most of the chatter is preoccupied with where to put this creature in a Darwinian phylogenetic tree. For a long time, animals were lumped together by their type of body cavity (coelom). That's changed; in 1997, Aguinaldo invented the category "ecdysozoa" ("molting animals") based on ribosomal RNA comparisons. This lumped together everything from butterflies to roundworms, from tardigrades ("water bears") to centipedes, from velvet worms to spiders. But is such a clade meaningful? "These disparate phyla are united by their means of molting, but otherwise share few morphological characters -- none of which has a meaningful fossilization potential." Smith and Caron note. "As such, the early evolutionary history of the group as a whole is largely uncharted."
The purpose of the grouping was to try to unite all the creatures that supposedly had a common ancestor. A more meaningful designation would account for the complexity and unique features of each animal, without forcing it into preconceived notions of common ancestry. Hallucigenia is a prime example. This creature had eyes, a mouth, teeth, a throat, a foregut, a stomach, and an anus. It had appendages that could reach its mouth. It had seven pairs of spines, each emerging from "a buttress of soft tissue," arranged with curvatures from front to back, protecting the entire animal. It had claws on the ends of the legs.
It's not just the cell types that need to be explained, but their arrangement into functional structures. These structures, moreover, need to be integrated into a functional animal in its ecosystem. And, they need software in some central nervous system that allowed the animal to use all of it. This is hierarchical organization, none of which is seen in the Precambrian layers beneath.
Just-So Storytelling
Live Science has a nice gallery of these and other Cambrian critters. Interesting  animals, but nothing new here. More of the same complexity. More of the same just-so storytelling that assumes undirected evolution. More distraction from the main question: what is the source of complex specified information to build a complex animal? How could it emerge from a blind, unguided process?

Friday 7 July 2017

Tactility v. Darwin.

Design at Your Fingertips: Researchers Struggle to Model Sense of Touch
Evolution News @DiscoveryCSC

The late pianist Victor Borge (1909-2000) was beloved not only for his comedy shtick but also for the sensitivity of his keyboard touch. He maintained the ability to interpret the most subtle pieces such as Claire de Lune (click on the image above to go there) with extreme delicacy all the way to age 90, when he was still giving 60 performances a year. It would be hard to design a robot with that level of durability, reliability, or sensitivity. Scientists know, because they’re having a hard time understanding it, let alone imitating it.


Four researchers from the University of Chicago and the University of Sheffield (UK) have made major progress over previous attempts to model the sense of touch. In a paper in the Proceedings of the National Academy of Sciences, “Simulating tactile signals from the whole hand with millisecond precision,” they announce their new mathematical model of a single hand’s neural responses under a variety of fingertip-touch experiments, hoping to assist robotics engineers wishing to imitate human touch response. Note the words code and information:

When we grasp an object, thousands of tactile nerve fibers become activated and inform us about its physical properties (e.g., shape, size, and texture). Although the properties of individual fibers have been described, our understanding of how object information is encoded in populations of fibers remains primitive. To fill this gap, we have developed a simulation of tactile fibers that incorporates much of what is known about skin mechanics and tactile nerve fibers. We show that simulated fibers match biological ones across a wide range of conditions sampled from the literature. We then show how this simulation can reveal previously unknown ways in which populations of nerve fibers cooperate to convey sensory information and discuss the implications for bionic hands. [Emphasis added.]

Unlike previous experiments that attempted to measure neural spikes from individual sensors in the skin of monkeys or humans, this new model simulates the responses of thousands of sensors based on knowledge of their classifications and distributions in the skin of the human hand. The team incorporated three classes of nerve fibers into the model:

  • Slowly adapting (SA) sensors: these respond primarily to spatial information from the stimulus.
    • Rapidly adapting (RA) sensors: twice as densely packed as SA sensors, these provide a mix of spatial and vibration responses.
    • Pacinian sensors: less densely packed than the other types, these neurons are sensitive to vibrations and waves generated by movement across the skin.
    Each of these fibers produces spike trains that encode different aspects of the stimulus, such as edges, compression, and vibration. One type alone might not convey much about the source, but together, they give the brain a rich array of data. Interpreted correctly, this information allows the brain to draw conclusions about size, shape, and texture of an object by touch alone. A blind person can thus “see” Braille letters with the fingertips where these neurons are most densely packed: “each fingertip contains just under 1,000 fibers,” the paper states, providing fine resolution, especially from the high-resolution SA1 fibers.

    The spike trains become more complex as the fingertip is moved into or across the source, activating more of the RA and PC fibers. Simply pressing a key on a computer keyboard is a complex act, with surrounding neurons becoming involved as pressure is applied or released. Moving a finger across a surface sets up waves that propagate throughout the hand, activating more sensors along the length of the finger and into the palm. This all happens within milliseconds (thousandths of a second), as it must when you consider the fast action of typing or playing a rapid piano piece. Even though PC fibers are less densely populated, their activity “dwarfs that of active SA1 or RA fibers,” the authors say, since they almost all become activated during a grasping operation or when feeling vibrations.

    The authors describe their efforts to “tune” or “fit” their model to known facts about neurons in the hand. Eventually, they achieved a good match for things like edge detection, edge orientation, and direction of motion for simple actions. Nevertheless, they omitted important capabilities such as temperature or pain — two important inputs that can generate reflex actions that activate arm muscles to jerk the hand away before the brain is aware of danger. Needless to say, their model completely overlooks things like sweat glands, blood vessels, immune cells, and all the other equipment packed into a fingertip.

    While the new model reflects admirable progress in understanding the sense of touch, and while it will undoubtedly help engineers seeking to improve prosthetic devices and robotic capabilities, the authors admit in the last section a number of limitations to their model. For instance, they tuned their model to information from rhesus macaques, knowing that humans have an additional type of tactile sensor called the SA2 fiber. They also fit their model to compression actions but not to sliding actions. In addition, they didn’t take fingerprints into account. Here’s why that could be a serious shortcoming of the model:

    Third, the skin mechanics model treats the skin as a flat surface, when in reality, it is not. The 3D shape of the skin matters during large deformations of the fingertip. For example, pressing the fingerpad on a flat surface causes the skin on the side of the fingertip to bulge out, which in turn, causes receptors located there to respond. Such complicated mechanical effects can be replicated using finite element mechanical models but not using the continuum mechanics (CM) model adopted here. To the extent that friction is a critical feature of a stimulus — for example, when sliding a finger across a smooth, sticky surface — or that the finger geometry plays a critical role in the interaction between skin and stimulus — as in the example of high-force loading described above — the accuracy is compromised. Under most circumstances, the model will capture the essential elements of the nerves’ response.

    Another limitation may be even more significant. They didn’t take into account the networking of responses in adjacent nerves. Their model treats an affected area as an isotropic “hotspot” wherein all the fibers react the same way, but nerve fibers are known to branch out and affect neighboring fibers. This can produce complex interactions between neurons, adding to the encoded tactile information the brain receives.

    Let’s dive one level deeper into the details to consider what goes on at the cellular level. A neuron embedded in the skin does not see anything. It “feels” the outer skin deforming slightly because it contains mechanosensitive portals in its membranes. These portals let some ions in, and others out, creating a wave train of signals down the cell’s length. That’s the electrical “spike” the authors talk about, but it doesn’t just happen without each neural cell first being equipped with molecular machines able to respond to pressure, and able to quickly reset and re-fire as the source changes. As the signals propagate toward the brain, the neurons must cross synapses that convert the electrical signals to chemical signals and back again, preserving the information and the timing of the signals as we saw in the case of 3-D hearing.

    Once again, the simplest, ordinary action of touching a fingertip on a surface is vastly more complex than we could conceive, challenging scientists to come up with simplified models to understand it. With this in mind, try an experiment: with your eyes closed, touch your index finger to a variety of surfaces around you: a table top, clothing, bread, liquid, the skin of your arm, a puff of air from your lips. Try to discern by touch alone information about each object’s friction, temperature, smoothness, shape, and hardness. Think of all those thousands of sensors providing that information to the brain with millisecond precision! Imagine what the brain has to deal with you when you plunge your whole body into a cold pool on a hot summer day.

    The authors say nothing about evolution in their paper. Design is so abundantly obvious in the human body, as Steve Laufmann discussed in his recent ID the Future podcasts about Howard Glicksman’s series on physiology, our best engineers cannot even conceive of approximating that level of functional coherence, performance and integration. Not even close.

    The undead in review.

    Jonathan Wells and Zombie Science — Reviewing the Reviewers

    On a new episode of ID the Future, Ray Bohlin gets biologist Jonathan Wells’s reaction to early responses to Wells’s new book, Zombie Science: More Icons of Evolution.

    Dr. Wells shares his favorite endorsement, discusses evolutionist Jerry Coyne’s “review” (Coyne admittedly didn’t read the book), and describes a spoof review that … well, listen and decide for yourself what you think the reviewer’s real message was.  Listen to it here, or download it here.

    Two billion year old tech Vs. Darwinism

    How Evolutionists Stole the Histones;
    Cornelius Hunter

    The recent finding that the DNA packaging technology and structure, known as chromatin, is not limited to eukaryotes but is also present in archaea, and so from an evolutionary perspective must have “evolved before archaea and eukaryotes split apart—more than 2 billion years ago,” is merely the latest in a string of misadventures evolutionists have incurred ever since they stole the histones.

    Histones are the hub-like proteins which (usually) serve as the hubs about which DNA is wrapped in the chromatin structure. Like a thread wrapped around a spool this design packs DNA away for storage with an incredible packing factor. Interestingly, the histone proteins are highly similar across vastly different species. Again, from an evolutionary perspective, this means they must have evolved early in evolutionary history to a very specific design. As one textbook explains:

    The amino acid sequences of four histones (H2A, H2B, H3, and H4) are remarkably similar among distantly related species. For example, the sequences of histone H3 from sea urchin tissue and of H3 from calf thymus are identical except for a single amino acid, and only four amino acids are different in H3 from the garden pea and that from calf thymus. … The similarity in sequence among histones from all eukaryotes indicates that they fold into very similar three-dimensional conformations, which were optimized for histone function early in evolution in a common ancestor of all modern eukaryotes. [1]

    But the new finding pushes back this evolutionary “optimization” far earlier in time. Once again, evolution’s heroics are moved to the distant past where no one can see. Early life was not simple.

    And of course DNA needs to be accessed so this histone packaging is quite dynamic. It can roll or it can be removed and moved. The histones themselves have tails that stick out and are tagged with small chemical groups that influence whether the packaging is tight or unrolled. Again, early life was not simple.

    But the fact that histones are so similar across a wide range of species leads to an entirely different dilemma for evolution. For from an evolutionary perspective, it means that the histones must not tolerate change very well. Here is how a leading 1994 textbook described it:

    When the number of amino acid differences in a particular protein is plotted for several pairs of species against the time since the species diverged, the result is a reasonably straight line. That is, the longer the period since divergence, the larger the number of differences. … When various proteins are compared, each shows a different but characteristic rate of evolution. Since all DNA base pairs are thought to be subject to roughly the same rate of random mutation, these different rates must reflect differences in the probability that an organism with a random mutation over the given protein will survive and propagate. Changes in amino acid sequence are evidently much more harmful for some proteins than for others. From Table 6-2 we can estimate that about 6 of every 7 random amino acid changes are harmful over the long term in hemoglobin, about 29 of every 30 amino acid changes are harmful in cytochrome c, and virtually all amino acid changes are harmful in histone H4. We assume that individuals who carried such harmful mutations have been eliminated from the population by natural selection. [2]

    So the reason the histone proteins are so similar, again from an evolutionary perspective, is because mutations changing those proteins could not be tolerated. This is the evolutionary prediction and here is how the next edition of that same textbook, eight years later in the year 2002, added to the discussion of the high similarity of the histone proteins:

    As might be expected from their fundamental role in DNA packaging, the histones are among the most highly conserved eucaryotic proteins. For example, the amino acid sequence of histone H4 from a pea and a cow differ at only at 2 of the 102 positions. This strong evolutionary conservation suggests that the functions of histones involve nearly all of their amino acids, so that a change in any position is deleterious to the cell. This suggestion has been tested directly in yeast cells, in which it is possible to mutate a given histone gene in vitro and introduce it into the yeast genome in place of the normal gene. As might be expected, most changes in histone sequences are lethal; the few that are not lethal cause changes in the normal pattern of gene expression, as well as other abnormalities.

    There was only one problem. That is false. In fact, even at the time studies had already shown that histone H4 could well tolerate many changes. It was not merely an example of evolution pointing in the wrong direction and producing yet another failed prediction. It was an all too frequent example of evolution abusing science, force-fitting results into its framework. And of course all of this became doctrine for wider consumption. As a 2001 PBS documentary stated:

    Histones interact with DNA in the chromosomes, providing structural support and regulating DNA activities such as replication and RNA synthesis. Their ability to bind to DNA depends upon a particular structure and shape. Virtually all mutations impair histone's function, so almost none get through the filter of natural selection. The 103 amino acids in this protein are identical for nearly all plants and animals.

    But it is not, and was not, true that “virtually all mutations impair histone’s function.” That was not science, it was dogma disguised as science. And since then the dogma has become even more obvious. As one recent paper summarized:

    Furthermore, recent systematic mutagenesis studies demonstrate that, despite the extremely well conserved nature of histone residues throughout different organisms, only a few mutations on the individual residues (including nonmodifiable sites) bring about prominent phenotypic defects.

    Similarly another paper bemoaned the confusing results:

    It is remarkable how many residues in these highly conserved proteins can be mutated and retain basic nucleosomal function. … The high level of sequence conservation of histone proteins across phyla suggests a fitness advantage of these particular amino acid sequences during evolution. Yet comprehensive analysis indicates that many histone mutations have no recognized phenotype.

    In fact, even more surprising for evolutionists, many mutations actually raised the fitness level:

    Surprisingly, a subset of 27 histone mutants show a higher intensity after growth (log2 ratio >+1.5) suggesting they are collectively fitter and maintain a selective advantage under glucose limitation.

    It was yet another falsified evolutionary prediction, and yet another example of evolution abusing science.

    Now evolutionists propose a redundancy hypothesis. Those histone mutations are well tolerated because evolution constructed a backup mechanism. Both mechanisms would have to mutate and fail before any lethal effects could be felt.

    As usual, contradictory results are accommodated by patching the theory with yet more epicycles. The epicycles make the theory far more complex, and far more unlikely, if that were so possible. In this case, evolution not only struck on incredible complexity, and did so early in history (before there were eukaryotes and nucleus’s in which to pack the DNA), but the whole design now must have incorporated layers of redundancy which we haven’t even been able to figure out yet.

    And all of this, evolutionists insist, must be a fact. Anyone who would so much as doubt this truth must be blackballed.

    It has been one misstep after another ever since the evolutionists stole the histones. Evolution is truly a profound theory, not for what it reveals about nature, but for what it reveals about people. Religion drives science, and it matters.

    1. H Lodish, A Berk, SL Zipursky, et al., Molecular Cell Biology, 4th ed. (New York: W. H. Freeman, 2000).

    2. B Alberts, D Bray, J Lewis, M Raff, K Roberts, J Watson, Molecular Biology of the Cell, 3rd ed. (New York: Garland Science, 1994), 243.



    3. B Alberts, A Johnson, J Lewis, et. al., Molecular Biology of the Cell, 4th ed. (New York: Garland Science, 1994), 243.

    Galapagos finches Vs. Darwin.

    Darwin’s Finches Are Evidence for Evolution? Think Again:
    By MICHAEL DENTON Published on February 11, 2016:


    Today is Darwin Day, marking the birthday of Charles Darwin. As the world looks back on the achievements of the great man, you are likely to see many “icons of evolution” triumphantly displayed. These famous, yet often flawed, success stories of Darwinian theory are held up as reasons to believe that the neo-Darwinian synthesis and everything it entails — scientifically and philosophically — has vanquished all legitimate challenges. But that is not so.

    One of the most famous such icons is a small group of birds, an inspiration for Darwin’s On the Origin of Species, that populates a remote cluster of islands in the equatorial Pacific. The Galápagos finches, with their different beak sizes, are brandished as one of the clearest examples of evolution at work.

    However, that is true up to only a very limited extent. These birds are, indeed, a clear example of micro-evolution. They are closely related to each other and their beaks have obviously been adapted through natural selection to the different food sources on the various islands. However, the finches also show what is required in order to expand the mechanism of natural selection to the larger or macro scale.

    The Galápagos finches put on display the two strict requirements that must be present in order for natural selection to work its magic. If these two factors are not present, natural selection is impotent to change any creature at all, much less create a new species.

    First, the finches’ beaks are clearly adaptive. Each distinct variation gives the lucky individual a definitive leg-up in its specific environment. There is an obvious, practical reason why the differentiation is helpful to the species in question. This is absolutely essential in order for natural selection to pick between variations in species. Natural selection can only “see” those variations that are adaptive — causing one individual to live, and carry on its genes, and another to die and not leave offspring. If a variation is neutral or does not somehow increase fitness in the specific environment the creature lives in, Darwin’s mechanism cannot select it.

    Second, there is a functional continuum among the finches’ beaks. That is, between a finch with a tiny beak and a finch with a large beak, there are tiny, step-by-step changes, and each change makes the creature slightly more fit in its environment. This is also essential for natural selection to work.

    The problem for Darwinian theory comes in explaining evolutionary change where, unlike the case of Darwin’s finches, these requirements are absent. First, there may not be a continuum. That is, natural selection cannot make large jumps or drastic changes. There must be small steps. Secondly, each single step must be beneficial to the individual. It is not enough for the first and last versions of the adaptation to be helpful — all the intervening steps must increase fitness as well.

    There are examples of creatures throughout the biological world that break one or both of these rules. Many creatures just don’t fit the natural selection story like the Galápagos finches do.

    For example, what is the adaptive significance of the many examples of geometric or abstract forms we see in the world, such as the shapes of leaves or the concentric whorls of flowers? Or consider the case of the enucleated red blood cell in mammals, which was the subject of my postdoctoral work. Not only have we found no obvious reason that such features increase fitness, there is no plausible continuum leading from a blood cell that keeps its nucleus to one that ejects it.

    There are no such intermediate forms in nature, and it is impossible to plausibly imagine intermediates that are even stable, much less adaptive. I document many more examples in my new book, Evolution: Still a Theory in Crisis.

    Without workable explanations for these many anomalies, Darwinian evolution may just go the way of Newtonian physics — applicable to a small area where specific rules apply, but unable to make universal statements about the world in general.

    So when you see the media promoting the Galápagos finches as evidence for Darwinian evolution this Darwin Day, take it with a grain of salt. Not every species in the world is as obliging to the requirements of Darwinism as the famous finches. And this is just the beginning of life’s richness and complexity that cannot be reduced to Darwinian biology.

    Thursday 6 July 2017

    On Darwinian attempts at explaining(away) human mathematical ability

    Explaining Human Mathematical Ability — Three Evolutionary Hypotheses

    Editor’s note: Last week we launched the new online college-level curriculum   to go with a beloved ID classic, The Design of Life: Discovering Signs of Intelligence in Biological Systems, by mathematician William Dembski and biologist Jonathan Wells. The curriculum is free and available here.  The 300-page book is hardcover, featuring full-color illustrations and accompanied by a CD with additional materials. Get it on Amazon now. Listen to Jonathan Wells talk about this package of amazing resources on an ID the Future podcast. And enjoy the following excerpt by Dr. Dembski and Dr. Wells:

    Humans have many unique cognitive abilities apart from language. Evolutionary theorists have proposed three main types of hypotheses for how these abilities might have evolved: the adaptationist hypothesis, the byproduct hypothesis, and the sexual selection hypothesis. Let’s consider these hypotheses in turn with respect to a specific cognitive ability, namely, mathematics.

    The Adaptationist Hypothesis
    How did humans acquire their talent for mathematics? According to the adaptationist hypothesis, mathematical ability conferred a selective advantage on our evolutionary ancestors. Those with better mathematical abilities were as a result better able to survive and reproduce. In other words, they were better able to “adapt” to their environments (hence the term “adaptationist hypothesis”). This hypothesis has a certain plausibility when it comes to the acquisition of rudimentary mathematical abilities like simple arithmetic.

    For example, if one of our hunter-gatherer ancestors counted five lions earlier in the day but now sees four of them dead (killed by him and his fellow hunters), a knowledge of basic arithmetic will warn him that one lion is still on the loose. He will thus know to act cautiously, which will translate into a survival and reproductive advantage. But rudimentary mathematical abilities are one thing; developing four-dimensional Riemannian geometries that describe a curved spacetime manifold, as Albert Einstein did, is quite another. It is hardly plausible that abstract mathematics, such as the Einstein Field Equations, confers any immediate survival and reproductive advantage. Moreover, future survival and reproduction is ruled out because evolution does not “look ahead.” So the adaptationist hypothesis breaks down, and other hypotheses are required.

    The Byproduct Hypothesis
    According to the byproduct hypothesis, higher cognitive functions like mathematics are not evolutionary adaptations at all. Instead, they are unintended byproducts of traits that are adaptive. Spectacular mathematical abilities are thus said to piggyback on adaptive traits. Pascal Boyer offers such an argument. According to him, some rudimentary ability to count and add is adaptive, but the capacity to do higher-level mathematics is a byproduct of this rudimentary ability. The higher-level capacity is not adaptive by itself; rather, it emerges as a free rider on abilities that are adaptive. But how, exactly, does rudimentary quantitative ability turn into the ability to develop curved spacetime Riemannian geometries or mathematical theories of comparable sophistication? Boyer doesn’t say.1

    This is always the weakness of byproduct hypotheses, namely, bridging the gap between what can be explained in standard evolutionary terms (adaptations) and the unexpected “freebies” (byproducts) that come along for the ride. Some free lunches are just too good to be true. And precisely when they are too good to be true, they require explanation. That’s especially true of mathematics: Here we have a human capacity that not only emerges, according to the byproduct hypothesis, from other capacities, but also provides fundamental insights into the structure of the physical universe (mathematics is, after all, the language of physics).2 How could a capacity like that arise as the byproduct of a blind evolutionary process, unguided by any intelligence? It is not a sufficient explanation here simply to say that it could have happened that way. Science does not trade in sheer possibilities. If our mathematical ability is the byproduct of other evolved traits, then the connection with those traits needs to be made explicit. To date, it has not been.

    The Sexual Selection Hypothesis
    Finally, we turn to the sexual-selection hypothesis. Sexual selection is Darwin’s explanation for how animals acquire traits that have no direct adaptive value. Consider a stag whose antlers are so large that they are more deadweight than defense. Or a peacock whose large colored tail makes it easy prey. How do such structures evolve? According to Darwin, they evolve because they help to attract mates—they are a form of sexual display. Thus, even though these features constitute a disadvantage for survival in the greater environment, the reproductive advantage they provide in attracting mates more than adequately compensates for this disadvantage and provides an evolutionary explanation for the formation of these features.

    Geoffrey Miller has applied Darwin’s idea of sexual selection to explain the formation of our higher cognitive functions.3 According to him, extravagant cognitive abilities like those exhibited by mathematical geniuses are essentially a form of sexual display. Once a capacity begins to attract mates, it acts like a positive feedback loop, continually reinforcing itself. In the case of cognitive functions, such a positive feedback loop can run unchecked because there are no environmental constraints to impose limits: unlike stag antlers or peacock tails, which can only get so large before their adaptive disadvantage outweighs their ability to attract mates, higher cognitive functions can essentially increase without limits. This, for Miller, is the origin of our higher cognitive functions, and our talent for mathematics in particular.

    The Fundamental Weakness of These Evolutionary Hypotheses
    Leaving aside whether mathematical ability really is a form of sexual display (most mathematicians would be surprised to learn as much), there is a fundamental problem with these hypotheses. To be sure, they presuppose that the traits in question evolved, which in itself is problematic. The main problem, however, is that none of them provides a detailed, testable model for assessing its validity. If spectacular mathematical ability is adaptive, as the adaptationist hypothesis claims, how do we determine that? What precise evolutionary steps would be needed to achieve that ability? If it is a byproduct of other abilities, as the byproduct hypothesis claims, of which abilities exactly is it a byproduct and how do these other abilities facilitate it? If it is a form of sexual display, as the sexual selection hypothesis claims, how exactly did the ability become a criterion for mate selection?

    In short, the main difficulty with all three hypotheses is that they attempt to account for an existing state of affairs without hard evidence of the factors that brought it about, only speculation. In the case of mathematics in particular, that is an especially severe deficit because higher mathematics is not obviously useful when it first emerges. The fact that uses are sometimes found later is, on conventional evolutionary grounds, irrelevant to its emergence. It becomes relevant only if one is justified in thinking that there is purpose in nature.

    Intelligent Design?
    Certainly, if evolution is true, then one of these hypotheses or some combination of them is likely to account for our ability to do mathematics. But even if evolution is true, in the absence of a detailed, testable model of how various higher-level cognitive functions emerged, these hypotheses are scientifically sterile. On the other hand, from an intelligent design perspective, mathematics is readily viewed as an inherent feature of intelligence and rationality. Moreover, the fact that the mathematical theorems we prove mirror the deep structure of physical reality suggests that intelligence is fundamental to nature and not merely an accidental or historical byproduct of blind material forces. The intelligence underlying nature as reflected in mathematics is a theme explored by Eugene Wigner, who referred to the “unreasonable effectiveness” of mathematics in elucidating nature.4

    Number Sense in Animals
    Many animals have a  basic ability to know the difference between more and less, or many and few. Rhesus monkeys and chimpanzees appear to pay more attention to a quantity if it has changed than if it hasn’t. According to M. D. Hauser, captive rhesus monkeys have been taught to understand ordinal relations from 1 to 9, but only after hundreds of training trials in conditions that are not duplicated in the wild.5 Essentially, after six months of training, some rhesus monkeys were accurate 50 percent of the time in identifying an ascending or descending order from 1 to 9.6 A weakness of this research is the high level of human interference, a point often overlooked in evolutionary literature (though not by Hauser). The monkeys develop this skill under intensive training by humans. It is unlikely that they would do so otherwise, because almost any non-destructive use of the average wild monkey’s time would be better and more immediately rewarded in nature. This fact tells against an adaptationist hypothesis in explaining even the most basic arithmetic skills, never mind abstract mathematical skills that typically only find a use after they have emerged apart from any survival goal.

    Notes:

    (1) Boyer makes this argument in Religion Explained: The Evolutionary Origins of Religious Thought (New York: Basic Books, 2001). In attempting to account for higher cognitive functions, Boyer is concerned not just with mathematics but also with art, religion, and ethics. For another byproduct approach to higher cognitive functions, see Steven Mithen, The Prehistory of the Mind: The Cognitive Origins of Art, Religion, and Science (London: Thames & Hudson, 1996). Mithen sees higher-level functions like mathematics as the byproducts of a “cognitive fluidity” that is adaptive in the sense that it facilitates the coordination and communication of various lower-level cognitive modules.

    (2) See especially Mark Steiner, The Applicability of Mathematics as a Philosophical Problem (Cambridge, Mass.: Harvard University Press, 1999).

    (3) See his book The Mating Mind: How Sexual Choice Shaped the Evolution of Human Nature (New York: Doubleday, 2000).

    (4) See Eugene P. Wigner, “The Unreasonable Effectiveness of Mathematics in the Natural Sciences,” Communications in Applied Mathematics 13 (1960): 1. For a deeper exploration of this theme, see Steiner, The Applicability of Mathematics as a Philosophical Problem.

    (5) M. D. Hauser, “What Do Animals Think about Numbers?” American Scientist 88 (2) (2000): 144–51.


    (6) Beth Azar, “Monkeying Around with Numbers,” Monitor on Psychology: Science Watch 31(1) (January 2000): available online here (last accessed June 7, 2006).

    Illiberal liberals?:Pros and Cons.

    Wednesday 5 July 2017

    How is Christ prototokos.

    "He is the image of the invisible God, the firstborn of all creation; because by means of him all [other] things were created in the heavens and upon the earth, the things visible and the things invisible, no matter whether they are thrones or lordships or governments or authorities. All [other] things have been created through him and for him. Also, he is before all [other] things and by means of him all [other] things were made to exists." (Col. 1:15-17, The New World Translation).

    cornerst writes: Please note that this passage does not say Jesus was the "first created," but that He was the "first-born." The Bible doesn't use the Greek word for "first created (protoktizo), but firstborn (prototokos) of all creation.

    Response: It should be noted that protoktizo was not in common use back in the first century, and would not be for a 100 to 200 years after Christ. Interestingly though, when this word was eventually used, it was used of Christ. John Patrick, in his Clement of Alexandria notes:

    "Clement repeatedly identifies the Word with the Wisdom of God, and yet refers to Wisdom as the first-created of God; while in one passage he attaches the epithet "First-created," and in another "First-begotten," to the Word." p.103,104, note 6.
    The Philosophy of the Church Fathers, Volume 1 Faith, Trinity, Incarnation, by Harry Austryn Wolfson, 2nd Edition, Revised:
    "Zahn casually remarks that Clement 'always makes a sharp distinction between the only uncreated God the Father and the Son or Logos who was begotten or created before the rest of creation.'...1. cf. Th. Zahn, "Supplementum Clementinium", (1884), 144, p. 204, 92 
    "It is undoubtably with reference to this "coming forth" of the Logos prior to the creation of the world that Clement speaks of the Logos as "firstborn" [protogonos] and of wisdom, which he idtentified with the Logos, as the "first-created" [protoktistos]...30 Strom. VI, Ibid. V. 14., ibid. p 209
    cornerst writes: The word "firstborn" refers to a position of pre-eminence rather than a time of birth. Rights and privileges were usually bestowed upon the child who was born first, but those rights did not always go to him. Manasseh was the first one born, but Jacob (Israel) blessed Ephraim instead of Manasseh and gave him the position of first-born (Gen. 48:13-22). In Jeremiah 31:9, God declares Ephraim to be His first-born, even though Manasseh was born first. 
    The same is true with Jacob and Esau. Although Esau was the first one born, Jacob (whose name was change to Israel) received his brother's birthright and his father's blessing and became the first-born. The nation of Israel was named after him, and the Lord calls Israel His first-born (Ex. 4:22). Here again, first-born refers to rank and privilege. It means first in importance, not first in time. The nation of Israel was not the first-born of a woman and not even the first nation to exist. But God called it the first-born among all the nations. In the same way, Jesus is the first-born of all creation. 
    The "first-born of the poor" (Isa. 14:30) means "the poorest of the poor." The "first-born of death" (Job 18:13) means Job's disease was the most terrible of diseases. The "first-born" of the kings means the highest of the kings of the earth (Ps. 89:27). David (v.20) was the last one born in his family, but was called the firstborn. The "first-born of the dead" (Col. 1:18, Rev. 1:5) means that Jesus is pre-eminent over death.
    Response: But how many of us know that the word PRWTOTOKOS is not used in Greek LXX in Job 18:13 and Isaiah 14:30? Let us look for examples where it is used mostly followed by the genitive like "of": 
    Verses used are from the English Translation of The Septuagint Version of the Old Testament by Sir Lancelot C. L. Brenton, 1844, 1851.

              LXX Genesis 4:4 And Abel also brought of the first born of his sheep 
              and of his fatlings, and God looked upon Abel and his gifts,

              LXX Genesis 25:13 And these are the names of the sons of Ismael, according 
              to the names of their generations. The firstborn of Ismael, Nabaioth, 
              and Kedar, and Nabdeel, and Massam,

              LXX Genesis 27:19 And Jacob said to his father, I, Esau thy 
              first-born, have done as thou toldest me; rise, sit, and eat of my 
              venison, that they soul may bless me.

              LXX Genesis 35:23 The sons of Lea, the first-born of Jacob; Ruben, 
              Symeon, Levi, Judas, Issachar, Zabulon.

              LXX Genesis 36:15 These are the chiefs of the son of Esau, even the sons of 
              Eliphas, the first-born of Esau; chief Thaeman, chief Omar, chief 
              Sophar, chief Kenez,

              LXX Genesis 38:6 And Judas took a wife for Er his first-born, whose 
              name was Thamar.

              LXX Genesis 38:7 And Er, the first-born of Judas, was wicked before 
              the Lord; and God killed him.

              LXX Genesis 46:8 And these are the names of the sons of Israel that went 
              into Egypt with their father Jacob-- Jacob and his sons. The first-born 
              of Jacob, Ruben.

              LXX Genesis 49:3 Ruben, thou art my first-born, thou my strength, and 
              the first of my children, hard to be endured, hard and self-willed.

              LXX Exodus 4:22 And thou shalt say to Pharao, These things saith the Lord, 
              Israel is my first-born.

              LXX Exodus 6:14 And these are the heads of the houses of their families: the 
              sons of Ruben the first-born of Israel; Enoch and Phallus, Asron, and 
              Charmi, this is the kindred of Ruben.

              LXX Exodus 11:5 And every first-born in the land of Egypt shall die, from 
              the first-born of Pharao that sits on the throne, even to the 
              first-born of the woman-servant that is by the mill, and to the 
              first-born of all cattle.

              LXX Exodus 12:29 And it came to pass at midnight that the Lord smote all the 
              first-born in the land of Egypt, from the first-born of Pharao that 
              sat on the throne, to the first-born of the captive-maid in the 
              dungeon, and the first-born of all cattle.

              LXX Exodus 13:13 Every offspring opening the womb of the ass thou shalt 
              change for a sheep; and if thou wilt not change it, thou shalt redeem it: 
              every first-born of man of thy sons shalt thou redeem.

              LXX Exodus 13:15 And when Pharao hardened his heart so as not to send us 
              away, he slew every first-born in the land of Egypt, both the first-born 
              of man and the first-born of beast; therefore do I sacrifice 
              every offspring that opens the womb, the males to the Lord, and every 
              first-born of my sons I will redeem.

              LXX Exodus 22:29 Thou shalt not keep back the first-fruits of thy threshing 
              floor and press. The first-born of thy sons thou shalt give to me.

              LXX Exodus 34:19 The males are mine, everything that opens the womb; every 
              first-born of oxen, and every first-born of sheep.

              LXX Exodus 34:20 And the first-born of an ass thou shalt redeem with 
              a sheep, and if thou wilt not redeem it thou shalt pay a price: every 
              first-born of thy sons shalt thou redeem: thou shalt not appear 
              before me empty.

              LXX Numbers 1:20 And the sons of Ruben the first-born of Israel 
              according to their kindreds, according to their divisions, according to the 
              houses of their families, according to the number of their names, according 
              to their heads, were-- all males from twenty years old and upward, every one 
              that went out with the host--

              LXX Numbers 3:40 And the Lord spoke to Moses, saying, Count every 
              first-born male of the children of Israel from a month old and upwards, 
              and take the number by name.

              LXX Numbers 3:41 And thou shalt take the Levites for me-- I am the Lord-- 
              instead of all the first-born of the sons of Israel, and the cattle 
              of the Levites instead of all the first-born among the cattle of the 
              children of Israel.

              LXX Numbers 3:45 Take the Levites instead of all the first-born of the 
              sons of Israel, and the cattle of the Levites instead of their cattle, 
              and the Levites shall be mine; I am the Lord.

              LXX Numbers 3:46 And for the ransoms of the two hundred and seventy-three 
              which exceed the Levites in number of the first-born of the sons of 
              Israel;

              LXX Numbers 3:50 He took the silver from the first-born of the sons of 
              Israel, a thousand three hundred and sixty-five shekels, according to 
              the holy shekel.

              LXX Numbers 8:16 For these are given to me for a present out of the midst of 
              the children of Israel: I have taken them to myself instead of all the 
              first-born of the sons of Israel that open every womb.

              LXX Numbers 8:17 For every first-born among the children of Israel is 
              mine, whether of man or beast: in the day in which I smote every 
              first-born in the land of Egypt, I sanctified them to myself.

              LXX Numbers 18:15 And every thing that opens the womb of all flesh, 
              whatsoever they bring to the Lord, whether man or beast, shall be thine: 
              only the first-born of men shall be surely redeemed, and thou shalt 
              redeem the first-born of unclean cattle.

              LXX Numbers 18:17 But thou shalt not redeem the first-born of calves 
              and the first-born of sheep and the first-born of goats; 
              they are holy: and thou shalt pour their blood upon the altar, and thou 
              shalt offer the fat as a burnt-offering for a smell of sweet savour to the 
              Lord.

              LXX Numbers 26:5 Ruben was the first-born of Israel: and the sons of 
              ruben, Enoch, and the family of Enoch; to Phallu belongs the family of the 
              Phalluites.

              LXX Deuteronomy 12:6 And ye shall carry thither your whole-burnt-offerings, 
              and your sacrifices, and your first-fruits, and your vowed-offerings, and 
              your freewill-offerings, and your offerings of thanksgiving, the 
              first-born of your herds, and of your flocks.

              LXX Deuteronomy 12:17 Thou shalt not be able to eat in thy cities the tithe 
              of thy corn, and of thy wine, and of thine oil, the first-born of thine 
              herd and of thy flock, and all your vows as many as ye shall have 
              vowed, and your thank-offerings, and the first-fruits of thine hands.

              LXX Deuteronomy 14:23 And thou shalt eat it in the place which the Lord thy 
              God shall choose to have his name called there; ye shall bring the tithe of 
              thy corn and of thy wine, and of thine oil, the first-born of thy herd 
              and of thy flock, that thou mayest learn to fear the Lord thy God 
              always.

              LXX Deuteronomy 15:19 Every first-born that shall be born among thy kine and 
              thy sheep, thou shalt sanctify the males to the Lord thy God; thou shalt not 
              work with thy first-born calf, and thou shalt not shear the first-born of 
              thy sheep.

              LXX Deuteronomy 33:17 His beauty is as the firstling of his bull, his 
              horns are the horns of a unicorn; with them he shall thrust the nations at 
              once, even from the end of the earth: these are the ten thousands of 
              Ephraim, and these are the thousands of Manasse.

              LXX Joshua 6:26 And Joshua adjured them on that day before the Lord, saying, 
              Cursed be the man who shall build that city: he shall lay the foundation of 
              it in his first-born, and he shall set up the gates of it in his 
              youngest son. And so did Hozan of Baethel; he laid the foundation in Abiron 
              his first-born, and set up the gates of it in his youngest surviving son.

              LXX Joshua 17:1 And the borders of the tribe of the children of Manasse, 
              (for he was the first-born of Joseph) assigned to Machir the 
              firstborn of Manasse the father of Galaad, for he was a warrior, were 
              in the land of Galaad and of Basan.

              LXX 2 Samuel 3:2 And sons were born to David in Chebron: and his 
              first-born was Ammon the son of Achinoom the Jezraelitess.

              LXX 2 Samuel 13:21 And king David heard of all these things, and was very 
              angry; but he did not grieve the spirit of his son Amnon, because be loved 
              him, for he was his first-born.

              LXX 1 Kings 16:34 And in his days Achiel the Baethelite built Jericho; he 
              laid the foundation of it in Abiron his first-born, and he set up the 
              doors of it in Segub his younger son, according to the word of the Lord 
              which he spoke by Joshua the son of Naue.

              LXX 1 Chronicles 1:29 And these are their generations: the first-born of 
              Ismael, Nabaeoth, and Kedar, Nabdeel, Massam,

              LXX 1 Chronicles 2:3 The sons of Juda; Er, Aunan, Selom. These three were 
              born to him of the daughter of Sava the Chananitish woman: and Er, the 
              first-born of Juda, was wicked before the Lord, and he slew him.

              LXX 1 Chronicles 2:13 And Jessae begot his first-born Eliab, Aminadab 
              was the second, Samaa the third,

              LXX 1 Chronicles 2:25 And the sons of Jerameel the first-born of Esron 
              were, the first-born Ram, and Banaa, and Aram, and Asan his brother.

              LXX 1 Chronicles 2:27 And the sons of Ram the first-born of Jerameel 
              were Maas, and Jamin, and Acor.

              LXX 1 Chronicles 2:42 And the sons of Chaleb the brother of Jerameel were, 
              Marisa his first-born, he is the father of Ziph:-- and the sons of 
              Marisa the father of Chebron.

              LXX 1 Chronicles 2:50 These were the sons of Chaleb: the sons of Or the 
              first-born of Ephratha; Sobal the father of Cariathiarim,

              LXX 1 Chronicles 3:15 And the sons of Josia; the first-born Joanan, 
              the second Joakim, the third Sedekias, the fourth Salum.

              LXX 1 Chronicles 4:4 And Phanuel the father of Gedor, and Jazer the father 
              of Osan: these are the sons of Or, the first-born of Ephratha, the 
              father of Baethalaen.

              LXX 1 Chronicles 5:1 And the sons of Ruben the first-born of Israel 
              (for he was the first-born; but because of his going up to his father's 
              couch, his father gave his blessing to his son Joseph, even the son Israel; 
              and he was not reckoned as first-born;

              LXX 1 Chronicles 5:3 The sons of Ruben the first-born of Israel; 
              Enoch, and Phallus, Asrom, and Charmi.

              LXX 1 Chronicles 6:28 The sons of Samuel; the first-born Sani, and 
              Abia.

              LXX 1 Chronicles 8:1 Now Benjamin begot Bale his first-born, and 
              Asbel his second son, Aara the third, Noa the fourth,

              LXX 1 Chronicles 8:30 And her first-born son was Abdon, and Sur, and 
              Kis, and Baal, and Nadab, and Ner,

              LXX 1 Chronicles 8:38 And Esel had six sons, and these were their name; 
              Ezricam his first-born, and Ismael, and Saraia, and Abdia, and Anan, 
              and Asa: all these were the sons of Esel.

              LXX 1 Chronicles 8:39 And the sons of Asel his brother; AElam his 
              first-born, and Jas the second, and Eliphalet the third.

              LXX 1 Chronicles 9:5 And of the Selonites; Asaia his first-born, and 
              his sons.

              LXX 1 Chronicles 9:36 And his first-born son was Abdon, and he had 
              Sur, and Kis, and Baal, and Ner, and Nadab,

              LXX 1 Chronicles 9:44 And Esel had six sons, and these were their names; 
              Esricam his first-born, and Ismael, and Saraia, and Abdia, and Anan, 
              and Asa: these were the sons of Esel.

              LXX 1 Chronicles 26:6 And to Samaias his son were born the sons of his 
              first-born, chiefs over the house of their father, for they were mighty.

              LXX Nehemiah 10:36 the first-born of our sons, and of our 
              cattle, as it is written in the law, and the first-born of our herds 
              and of our flocks, to bring to the house of our God, for the 
              priests that minister in the house of our God.

              LXX Psalm 135:8 Who smote the first-born of Egypt, both man and 
              beast.

              LXX Psalm 136:10 To him who smote Egypt with their first-born; for 
              his mercy endures for ever.

              LXX Jeremiah 31:9 (38:9) They went forth with weeping, and I will bring them 
              back with consolation, causing them to lodge by the channels of waters in a 
              straight way, and they shall not err in it: for I am become a father to 
              Israel, and Ephraim is my first-born.

              LXX Micah 6:7 Will the Lord accept thousands of rams, or ten thousands of 
              fat goats? should I give my first-born for ungodliness, the fruit of 
              my body for the sin of my soul?

    As you can see there are many examples of the firstborn[PRWTOTOKOS] as a separate,  subordinate, and most of the time the actual FIRST BORN member of a family. 
    It should be noted too,  that Jesus, unlike Ephraim, Jacob and Israel, was never GIVEN the title of "firstborn". He was simply spoken of as firstborn in the temporal sense in passages like the ones at Col. 1:15, 18, Heb. 1:6, Rev. 1:5 and Romans 8:29. 
    When this changes, "the firstborn of" is used as part of a group. If it is "the firstborn of" Israel(Ex. 6:14), it is one of the sons of Israel, if it is "the firstborn of" Pharoah(Ex. 11:5) it is a member of the house of Pharoah, if it is "the firstborn of" beasts(Ex. 13:15) then it is an animal also. Why then should this rule be changed as it applies to "the firstborn of" creation? Obviously Jesus is a created being, as he was historically always thought to be the Wisdom of Proverbs. Is this a stretch?
    "She [Wisdom] is God's associate in his works, and his agent in making all things (Prov 8:22-30; see also Jn 1:3; Col 1:16; Heb 1:2)." footnote at Wisdom 8:2-21 in the New Oxford Annotated Bible-NRSV 
    "The doctrine of wisdom, thus outlined in the OT, will be resumed in the NT which will give it new and decisive completion by applying it to the person of Christ 
    Jesus is referred to as Wisdom itself, the Wisdom of God, Mt 11:19 par.; Lk 11:49, cf. Mt 23:34-36; 1 Co 1:24-30; like Wisdom, he participates in the creation and preservation of the world, Col 1:16-17, and the protection of Israel, 1Co 10:4, cf. Ws 10:17seq. 
    Finally, John in his prologue attributes the characteristics of creative Wisdom to the 
    Word, and his gospel throughout represents Christ as the Wisdom of God. See Jn 6:35t. 
    Hence, Christian tradition from St Justin onwards sees in the Wisdom of the OT the 
    person of Christ himself." footnote New Jerusalem Bible at Prov 8.
    Why is this damaging to Trinitarians? Because Wisdom was created!
    "He created me from the beginning, before the world, and I shall never cease."Sirach24:9 
    The Interpreter's Bible [p.830] says of Prov 8:22: "The verb QANAH may be translated either way. In view of the statements made in the following verses concerning wisdom, it would seem that the RSV translates correctly; cf. also the following quotations from Ecclesiasticus:
    Wisdom was created before them all, 
    And sound intelligence from eternity (Ecclus 1:4)

    The Lord himself created her (Ecclus 1:9

    Then the Creator of all gave me his command; 
    And he who created me made my tent rest (Ecclus 24:8 AT)."

    Also see Proverbs 8:22 NRSV, "The LORD created me at the beginning of his work."

    "The LORD formed me as the first of his works, the beginning of 
    his deeds of old." Smith&Goodspeed


    cornerst writes:The New World Translation adds the word "other" four times, which is not in the Greek. They add to Scripture to make it look like Jesus was the first-created thing among God's creation. According to Jehovah's Witnesses, God created Jesus and then Jesus created all other things. This mistranslation of Col. 1:16-17 presents a problem for the Jehovah's Witnesses. Isaiah 44:24 says, "Thus says the LORD, your Redeemer, and the one who formed you from the womb, 'I, the LORD, am the maker of all things, stretching out the heavens by Myself, and spreading out the earth all alone'". How is it possible for the LORD (Jehovah) to stretch out the heavens alone and yet Jesus, "the first created thing," be the one who did it? They can't both be true. Jesus is not the created, but the Creator (John 1:3,10, Heb. 1:10, Col. 1:16).

    Response: Well let us see if John 1:3,10, Heb. 1:10, Col. 1:16 picture Jesus as the creator.

    "And, Thou, Lord, in the beginning didst lay the foundation of the earth, And the heavens are the works of thy hands". Heb. 1:10 ASV 
    In Hebrews 1:10-12 the apostle Paul uses a scripture earlier applied to Jehovah in Ps. 102. Does that make them the same person? No! For instance verse 8 says, "But of the Son [he saith,] 
    Thy throne, O God, is for ever and ever; And the sceptre of uprightness is the sceptre of thy kingdom." These words were earlier applied to King Solomon in Ps. 45:6 (see also 2Sam. 7:14). Is King Solomon  the same person as Jesus? No! Jesus is simply doing a work earlier prefigured by Solomon, also sharing some of the qualities of Solomon, such as wisdom. So when it comes to Jehovah in Ps. 102 the writer here attributes these qualities to Jesus Christ, because Jesus is the one whom God used in the work of creation and to whom he has now committed all authority "in heaven and on the earth." (Matt. 28:18; Col. 1:15-17) Jesus represents the God that no one has ever seen to us fully in all his qualities and actions.(John 1:18) 
    Psalm 22, attributed to David, relates, partly in figurative language, some of the sufferings of Christ. (Compare Psalm 22:1 with Mark 15:34; also compare the entire psalm with the four gospel accounts of Jesus' trial and impalement.) Are Jesus and David the same person? No! A scripture in Matthew 2:15 applies to Jesus, but the earlier reference in Hosea 11:1 applies to Israel. Does than make them the same? No! There is a prophecy about Elijah in Malachi 4:5 that is applied to John the Baptist in Matthew 17:12,13; 11:14. Is John the Baptist really Elijah? No! They just did a similar work. I think you get the point. For more on this verse, click here.

    "John 1:3 All things were made through him; and without him was not anything made 
    that hath been made.  {1:10} He was in the world, and the world was made 
    through him, and the world knew him not." ASV 
    In looking at the Greek word here for "apart from" CWRIS, Thayer's Greek Lexicon says of its occurence in John 1:3 "without the intervention (participation or co-operation) of one." 
    In this way, the Bible in Living English handles it superbly, "Everything was made by his agency." Jn 1:3 
    Even Origen acknowledged this, "And the apostle Paul says in his epistle to the Hebrews: 'At the end of the days He spoke to us in his Son, whom He made heir of all things, 'through whom' also He made the ages, " showing us that God made the ages through His Son, the 'through whom' belonging, when the ages were made to the Only-begotten. Thus if all things were made, as in this passage also, THROUGH [DIA] the Logos, then they were not made by the Logos, but by a stronger and greater than He. And who else could this but the Father?" 
    Origen's Commentary on John, ANF 10, Book 2, chap. 6, p. 328 
    This scripture ties into the next one at Colossians 1:16. As we can see, the world was made "through him". We have already seen that Wisdom  was created, but he was also with him at creation. "When he marked out the foundations of the earth; Then I was beside him, like a master workman; And I was daily his delight, rejoicing before him always." Prov. 8:29, 30 RSV 
      The bible tells us that the angels were there too:"Where wast thou when I laid the foundations of the earth? Declare, if thou hast understanding....When the morning stars sang together, And all the sons of God shouted for joy? Job 38:4,7 ASV But as we can see from Proverbs, Wisdom/Jesus shared a special relationship with his God Jehovah. 
    Col 1:16 "for in him were all things created, in the heavens and upon the earth, 
    things visible and things invisible, whether thrones or dominions or principalities or powers; all things have been created through him, and unto him" ASV 
    Again we see that all things were "created thru him". This is only right, after all the Bible says: "For there is one God, one mediator also between God and men, [himself] man, Christ Jesus." 1 Tim. 2:5 ASV Now a mediator cannot be the person he is mediating for. For instance Moses is also called a mediator at Gal. 3:19. Moses, like Jesus,  shared a special relationship with God. Both were even called by the respectful title "god", (Ex. 7:1; John 1:1) though Jesus is mightier than Moses. (Is. 9:6) 
    But let us expand further. Let us look at Hebrews 1: 
    "In the past God spoke to our ancestors many times and in many ways through the prophets, {1:2} but in these last days he has spoken to us through his Son. He is the one through whom God created the universe." TEV 
    In verse 1, God spoke. The prophets were intermediate agents (Greek: EN). 
    God uses agents to carry out his will. 
    In verse 2, God spoke, but just like the prophets,  the Son was an intermediate agent (Greek: EN). 
    For example, Col 1:16 does not teach that Jesus is the almighty creator. Rather, it uses same Greek preposition EN which is used of the Son with an active source in the context (like the Father in vss. 12 and 13). The Father redeems "BY/IN/THROUGH" (Greek: EN) the Son. The Father creates "BY/IN/THROUGH" (Greek: EN) the Son. Since the Father creates "BY/IN/THROUGH" Son as agent, it is necessary that the creation of the Son was a special case. That is why Paul explicitly says that the Son is the "firstborn of" all creation ( PRWTOTOKOS), the "first-begotten of all creatures" Tyndale. Tyndale also refers to Jesus in Rev. 3:14 as the "beginning of the creatures of God."

    In John 1:3 it is clear that agency is intended since DIA is used with a passive verb, or created "THROUGH" (not "by") the Word. That "through" is the clear meaning and not "by" is made explicitly clear by Paul when he said of the relationship between God and Christ in 1 Cor 8:5,6: "One God, the Father, out of (Greek: EK) whom all things are, and we unto him; and one lord, Jesus Christ "through" (Greek: DIA) whom all things are, and we through him. "

    When you consider all the times that God and Christ Jesus are mentioned in Colossians, the  Spirit is mentioned a scant 2 times. Hardly a Trinity! "You simply simply cannot find the doctrine of the Trinity set out anywhere in the Bible. St Paul has the highest view of Jesus' role and person, but nowhere does he call him God. Nor does Jesus himself explicitly claim to be the second person of the Trinity, wholly equal to his heavenly Father." -- For Christ's Sake by Tom Harpur (Anglican Priest).

    It should be noted that Trinitarians do not beleive that Jesus is the Father. They believe that the Father is God, and that the Son, Jesus, is equally God. Yet they are not the same, but at the same time they are not plural, but one. So when trinitarians say that Jesus is God, they don't really mean that. What they mean is that Jesus is God the Son, the second person of a consubstantial Trinity. A phrase that is never used in the Bible!

    cornerst writes: The New World Translation adds the word "other" four times, which is not in the Greek.

    Response: Now let's look at the insertion of the word "other" in the New World Translation at 
    Colossians chapter 1. We are going to start of by looking at some other scriptures where this is 
    done. 
    Luke 21:29 
    "Look at the fig tree, and all the trees." Revised Standard Version (RSV) 
    "Think of the fig tree and all the other trees." Good News Bible (TEV) 
    "Consider the fig tree and all the other trees." New American Bible(NAB)

    Luke 11:42 
    "and every herb." Revised Version(RV) 
    "and of every [other] vegetables." NWT 
    "and all the other herbs." TEV 
    "and all other kinds of garden herbs." New International Version

    In both these instances the word "other" was not in the original text, but translators felt a need 
    to put it in there. Can they do that even without brackets? 
    "A Greek Grammar of the New Testament and Other early Chrisitian Literature" by F. Blass and 
    A. Debrunner states that it is not uncommon for the greek to omit the word "other". 
    The book Theology and Bias in Bible Translations by Professor Rolf Furuli when talking about 
    the word "other" in the Col. 1:16 in the NWT says, "This means that the brackets that NWT uses 
    around OTHER may be removed, because the word OTHER is no addition or interpolation, but 
    in a given context it is a legitimate part of PAS."

    Have you ever noticed all those words in italics in the King James Version and the New American Standard Version? Those are words that are not in the original text, yet there are thousands of them.