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Tuesday 23 January 2018

Evo-devo v. Darwin.

How Embryonic Development Bears on Evolution
Cornelius Hunter

In order for evolution to have occurred as the orthodox theory describes, the intricate embryonic development stages of species must have evolved. Indeed, the developmental pathways of the species would be crucial in such a process. If we are to believe the evolutionary claim that the species spontaneously arose, then untold embryonic development pathways must have somehow undergone massive change.

But while evolutionists expected the study of such evolution of development to yield great insight into the evolutionary process and history, it has underwhelmed. This shortcoming is well known, as exemplified in a 2015 paper, The Comet Cometh: Evolving Developmental Systems“:

First, traditional comparative approaches to the evolution of development — whether focused on the morphological or on the molecular/genetic level — are reaching their limits in terms of explanatory power.

Except that this is an overstatement. To say that comparative approaches “are reaching their limits in terms of explanatory power” is to suggest that there was, at one time, some significant level of explanatory power provided. That would be a very optimistic interpretation of the data.

The paper continues:

The more we learn about the evolution of pattern-forming gene networks, or the ontogeny of complex morphological traits, the more it becomes clear that it is less than straightforward to conclude anything about evolutionary origins or dynamics based on such comparisons alone.

“Less than straightforward”? Let’s be clear — a more accurate descriptor would be “impossible.” In fact, the evidence does not reveal an evolutionary history, but rather is supported by the theory. Evolutionary theory does not follow the data, as Huxley prescribed, but rather the data follow the theory.

The paper continues:

On the one hand, homoplasy or convergent evolution abounds at all levels of investigation. One of the most lauded major insights of EvoDevo is that a common toolkit of genes and signaling pathways is reused over and over again to create a large diversity of different body plans, shapes, and organs.

Most lauded major insights? That would be the mother of all euphemisms. Evolutionists are always rationalizing devastating contradictions as teachable moments, and here we have yet another example. To cast the nonsensical finding of a “common toolkit” as a “major insight” is laughable.

This becomes clear as the paper continues:

Because of this, similarities in gene expression patterns or morphological structure often do not necessarily imply common ancestry, since they may as well reflect the frequent reuse of the same regulatory or morphogenetic modules.

Profound similarities “do not necessarily imply common ancestry.” We have now entered a Lewis Carroll world, as Elliott Sober would put it. The whole point of evolution was that such similarities revealed and mandated common descent. But now, we have the exact opposite, as similarities cannot be due to common descent, but must have arisen independently. And this is an “insight”? A fundamental prediction is demolished and evolutionists do not skip a beat. This is not science.

But it gets worse:

On the other hand, developmental system drift allows conserved networks to change considerably in terms of their component genes and regulatory interactions without changing the phenotypic outcomes such systems produce. This means that even functionally conserved regulatory networks can become unrecognizably divergent at the molecular and genetic level, especially across large evolutionary time spans.

We have now reached the height of absurdity. First, profound developmental similarities were found which could not be ascribed to common descent. Now we find that those developmental pathways which can (theoretically) be ascribed to common descent are profoundly different.


When will this bad dream end? The science contradicts the theory. Over. And over. And over. And over.

Some straight talk re: Human origins.

An Uncommonly Clear Discussion of Human Origins
David Klinghoffer | @d_klinghoffer

It’s not often that you hear the problem of human origins and the fossil record stated as plainly and lucidly as biologist Ann Gauger does in a new ID the Future episode. Dr. Gauger is CSC Director of Science Communications, and she chatted with Sarah Chaffee about the new book Theistic Evolution: A Scientific, Philosophical, and Theological Critique. Gauger explains that there’s a gap of about a million years between when Australopithecines seem to depart from the fossil record and when modern humans unambiguously appear – the latter at about 2 million year ago. What do you suppose happened there?

The purported transitional fossils in between are extremely scarce and fragmentary. Perhaps enough to fill a shoebox, as one scientist has estimated, they are what theistic evolutionists point to in demanding that we accept the standard evolutionary story. A helpful discussion – listen to the podcast or download it here.

Yet more on OOL science's RNA world narrative.

About That RNA World Hypothesis
Cornelius Hunter



Given its widespread popularity and acceptance you might not have realized that the so-called RNA World hypothesis suffers from some dramatic problems. At the top of the list is the rather awkward fact that there is no evidence for it. While skeptics have pointed this out for years, we now see evolutionists coming clean on this inconvenient truth as well. To wit, here is how Peter Wills and Charles Carter open their recent BioSystems  paper:

The RNA World is a widely-embraced hypothetical stage of molecular evolution, devoid of protein enzymes, in which all functional catalysts were ribozymes. Only one fact concerning the RNA World can be established by direct observation: if it ever existed, it ended without leaving any unambiguous trace of itself.

Even this is a bit of an understatement. Because without the prior assumption of evolution, which can and has underwritten a wide range of speculation, there is precisely zero reason to believe this wild hypothesis. No organisms have ever been discovered that demonstrate the RNA World hypothesis in action. Nor have scientists ever constructed any such organisms in their laboratories. This is not too surprising because no one has even produced anything remotely close to a detailed design of how such organisms could function.

Wills and Carter also point out negative evidences such as catalysis (RNA enzymes lack the ability to function over a wide range of temperatures) and the “impossible obstacles” to the hypothetical yet necessary transition from the RNA World to something resembling today’s extant cells. As Carter explains:

Such a rise from RNA to cell-based life would have required an out-of-the-blue appearance of an aaRS [aminoacyl-tRNA synthetase]-like protein that worked even better than its adapted RNA counterpart. That extremely unlikely event would have needed to happen not just once but multiple times — once for every amino acid in the existing gene-protein code. It just doesn’t make sense.

Indeed, it just doesn’t make sense. And yet in spite of these obvious problems, the RNA World has been a textbook staple, presented as a plausible and likely example of how early life evolved.

Saturday 20 January 2018

On the book of Genesis:The Watchtower Society's commentary

GENESIS, BOOK OF

The first book of the Pentateuch (Greek for “five rolls” or “fivefold volume”). “Genesis” (meaning “Origin; Birth”) is the name given to the first of these books by the Greek Septuagint, whereas its Hebrew title Bereʼ·shithʹ (In the Beginning) is taken from the first word in its opening sentence.

When and Where Written. The book of Genesis was evidently part of the one original writing (the Torah), and it was possibly completed by Moses in the wilderness of Sinai in the year 1513 B.C.E. After Genesis 1:1, 2 (relating to the creation of the heavens and the earth), the book evidently covers a span of thousands of years involved in the preparation of the earth for human habitation (see CREATION; DAY), and thereafter it covers the period from man’s creation on down to the year 1657 B.C.E., when Joseph died.—See CHRONOLOGY (From Human Creation to the Present).

Writership. The objection once raised by some skeptics that writing was not known in Moses’ day is today generally discounted. In his book New Discoveries in Babylonia About Genesis (1949, p. 35), P. J. Wiseman points out that archaeological research gives ample proof that “the art of writing began in the earliest historical times known to man.” Virtually all modern scholars acknowledge the existence of writing long before the time of Moses (in the second millennium B.C.E.). Expressions such as that found in Exodus 17:14, “Write this as a memorial in the book,” substantiate the fact that writing was in common use in Moses’ day. Adam must have had the ability to devise a form of writing, God having given him, as a perfect man, a language, with the ability to handle it perfectly, even to the extent of composing poetry.—Ge 2:19, 23.

From where did Moses get the information he included in Genesis?

All the information contained in the book of Genesis relates to events that took place prior to Moses’ birth. It could have been received directly by divine revelation. It is obvious that someone had to receive the information relating to the events prior to man’s creation in that way, whether Moses or someone prior to him. (Ge 1:1-27; 2:7, 8) This information and the remaining details, however, could have been transmitted to Moses by means of oral tradition. Because of the long life span of men of that period, the information could have been passed from Adam to Moses through just five human links, namely, Methuselah, Shem, Isaac, Levi, and Amram. A third possibility is that Moses obtained much of the information for Genesis from already existing writings or documents. As far back as the 18th century, the Dutch scholar Campegius Vitringa held this view, basing his conclusion upon the frequent occurrence in Genesis (ten times) of the expression (in KJ) “these are the generations of,” and once “this is the book of the generations of.” (Ge 2:4; 5:1; 6:9; 10:1; 11:10, 27; 25:12, 19; 36:1, 9; 37:2) In this expression the Hebrew word for “generations” is toh·le·dhohthʹ, and it is better rendered “histories” or “origins.” For example, “generations of the heavens and of the earth” would hardly be fitting, whereas “history of the heavens and the earth” is meaningful. (Ge 2:4) In harmony with this, the German Elberfelder, the French Crampon, and the Spanish Bover-Cantera all use the term “history,” as does the New World Translation. There is no doubt that even as men today are interested in an accurate historical record, so they have been from the start.

For these reasons, Vitringa and others since have understood each use of toh·le·dhohthʹ in Genesis to refer to an already existing written historical document that Moses had in his possession and that he relied upon for the majority of the information recorded in Genesis. They believe that the persons named in direct connection with such ‘histories’ (Adam, Noah, Noah’s sons, Shem, Terah, Ishmael, Isaac, Esau, and Jacob) were either the writers or original possessors of those written documents. This, of course, would still leave unexplained how all such documents came to be in the possession of Moses. It also leaves unexplained why documents obtained from men who were not distinguished as faithful worshipers of Jehovah (such as Ishmael and Esau) should be the source of much of the information used. It is entirely possible that the expression “This is the history of” is simply an introductory phrase serving conveniently to divide off the various sections of the long overall history. Compare Matthew’s use of a similar expression to introduce his Gospel account.—Mt 1:1; see WRITING.

No definite conclusion can be arrived at, therefore, as to the immediate source from which Moses obtained the information he recorded. Rather than just by one of the methods discussed, the information may have been received by all three, some through direct revelation, some through oral transmission, some by written records. The important point is that Jehovah God guided the prophet Moses so that he wrote by divine inspiration.—2Pe 1:21.

The material was to serve as an inspired guide to future generations. It was to be read to the people on frequent occasions (De 31:10-12; 2Ki 23:2, 3; Ne 8:2, 3, 18), and Israel’s kings were to take instructions from it.—De 17:18, 19.

The “Documentary Theory” of Critics. A theory has been set forth by some Bible critics that Genesis is not the work of one writer or compiler, namely, Moses, but rather that it represents the work of several writers, some of these living long after Moses’ time. On the basis of supposed differences of style and word usage, they have advanced the so-called documentary theory. According to this theory, there were three sources, which they call “J” (Jahwist), “E” (Elohist), and “P” (Priest Codex). Because of a double mention of a certain event or because of similarity of accounts in different parts of Genesis, some would add still further sources to the list, going so far in dissecting the book of Genesis as to claim that there were up to 14 independent sources. They contend that these various sources or writers held different views and theologies yet that, nevertheless, Genesis as an amalgamated product of these sources somehow forms a connected whole. There are many absurdities to which they go to support their theories, a few of which may be mentioned.

The original basis for the documentary theory was the use of different titles for God; the critics claim that this indicates different writers. The unreasonableness of such a view, however, can be seen in that in just one small portion of Genesis we find the following titles: “the Most High God” (ʼEl ʽEl·yohnʹ, Ge 14:18); “Producer of heaven and earth” (14:19); “Sovereign Lord” (ʼAdho·naiʹ, 15:2); “God of sight” (16:13); “God Almighty” (ʼEl Shad·daiʹ, 17:1); “God” (ʼElo·himʹ, 17:3); “the true God” (ha·ʼElo·himʹ, 17:18); “the Judge of all the earth” (18:25). Trying to use this as a basis for attributing each of these sections to a different writer produces insurmountable difficulties and becomes absurd. Rather, the truth is that the different titles applied to God in Genesis are used because of their meaning, revealing Jehovah in his different attributes, in his various works, and in his dealings with his people.

Other examples are: Because of the use of the word ba·raʼʹ, “created,” Genesis 1:1 is said to be written by the source called “P.” Yet we find the same word at Genesis 6:7 in the source supposed to be “J.” The expression “land of Canaan” appearing in several texts (among which are Ge 12:5; 13:12a; 16:3; 17:8) is said to be a peculiarity of the writer known as “P,” and therefore these critics hold that “P” wrote these passages. But in chapters 42, 44, 47, and 50, we find the same expression in the writings attributed by the same critics to “J” and “E.” Thus, while the critics claim that their theories are needed to account for supposed inconsistencies in Genesis, examination shows that the theories themselves are riddled with inconsistencies.

If the material attributed to each theoretical source is extricated portion by portion, and sentence by sentence, from the Genesis account and then reassembled, the result is a number of accounts each one of which by itself is illogical and incoherent. If we were to believe that these various sources were used and put together by a later compiler, we would be forced to believe that these incoherent accounts, before being amalgamated, were accepted as historical and were used for centuries by the nation of Israel. But what writer, especially a historian, would even construct such disconnected narratives, and if he did, what nation would accept them as a history of its people?

Illustrating the unreasonableness of the advocates of the “documentary theory” is this statement by Egyptologist K. A. Kitchen: “In Pentateuchal criticism it has long been customary to divide the whole into separate documents or ‘hands’. . . . But the practice of Old Testament criticism in attributing these characteristics to different ‘hands’ or documents becomes a manifest absurdity when applied to other ancient Oriental writings that display precisely similar phenomena.” He then cites an example from an Egyptian biography that might, using the theoretical methods employed by the critics of Genesis, be attributed to different “hands” but which work the evidence shows “was conceived, composed, written, and carved within months, weeks, or even less. There can be no ‘hands’ behind its style, which merely varies with the subjects in view and the question of fitting treatment.” (The New Bible Dictionary, edited by J. Douglas, 1980, p. 349) The weakness of the critics’ theories actually gives added strength to the evidence that only one man, Moses, recorded the connected, coherent account found in Genesis as inspired by God.

The Historical Character of Genesis. Genesis is the only source known to humans that provides a logical, coherent history of things back to the beginning. Without its factual history of the first man and woman, we would be left with the fanciful stories or allegorical explanations of man’s beginning that are found in the creation accounts of pagan nations. A comparison of the book of Genesis with the pagan creation accounts clearly demonstrates the superiority of the Bible account.

Thus, the principal Babylonian myth says that the god Marduk, the chief god of Babylon, killed the goddess Tiamat, then took her corpse and “split her like a shellfish into two parts: Half of her he set up and ceiled it as sky.” So the earth and its sky came into existence. As to the creation of human life, this myth states that the gods caught the god Kingu and they “imposed on him his guilt and severed his blood (vessels). Out of his blood they fashioned mankind.” (Ancient Near Eastern Texts, edited by James Pritchard, 1974, pp. 67, 68) Egyptian creation myths likewise involve the activities of several gods, but they disagree as to which city’s god (that of Memphis or that of Thebes) was the one who conceived the creation. One Egyptian myth relates that the sun-god Ra created mankind from his tears. Greek myths parallel those of the Babylonians. Ancient Chinese records are mostly calendars and chronological calculations or records of merely local or temporary interest.

Not one of such ancient sources furnishes us with the history, genealogy, and chronology that the book of Genesis provides. The writings of the ancient nations in general show uncertainty and confusion as to who their national founders were. The definiteness and detail with which Israel’s early history is presented is strikingly different. In reality we should not expect it to be otherwise, in view of God’s purpose toward his people. The Bible tells us that the nation of Israel was directly governed by God and that he dealt with their forefathers, especially Abraham, Isaac, and Jacob. Then he used Moses in a very special way, through him giving Israel the Law that established them as a nation. Israel’s history is in recorded form not only for Israel’s benefit but also for the benefit of all who will learn of the ways and dealings of the true God and serve him.

In answering those who would reject many portions of Genesis as fables or folklore, Wilhelm Möller says: “I do not think that it can be made plausible, that in any race fables and myths came in the course of time more and more to be accepted as actual facts, so that perchance we should now be willing to accept as historical truths the stories of the Nibelungenlied or Red Riding Hood. But this, according to the critics, must have been the case in Israel.” (The International Standard Bible Encyclopædia, edited by J. Orr, 1960, Vol. II, p. 1209) He goes on to point out that the prophets accepted the account of the destruction of Sodom and Gomorrah as correct (Isa 1:9; Am 4:11) and that they accepted Abraham, Isaac, Jacob, and Joseph as real persons. (Isa 29:22; Mic 7:20) Not only this, but in the Christian Greek Scriptures, Abraham is mentioned in many places, even by Jesus Christ at Matthew 22:32, in connection with the argument about the resurrection. If Abraham, Isaac, and Jacob had not really lived, Jesus would have used another illustration.—Mt 22:31-33.

Value of the Book. Genesis tells us how the universe came into being. In a matter-of-fact way it describes the wonders of creation, without making these overshadow the main purpose of the book. It is thus unlike the pagan creation stories that make these marvels the main thing and go to absurdities and obvious untruths to stress them. Genesis tells about the work of creation, and it shows God’s purpose in creating man, the relationship of man to God, and the relationship of man to the animals. It gives us the reason for death and trouble experienced by mankind and the hope of deliverance. It points out that all humans descended from the one man Adam, who sinned and lost life for his posterity; it thereby enables us to understand how the ransom sacrifice of one man, Jesus Christ, could atone for the sins of mankind. Genesis enables us to see how the issue of the rightfulness of God’s sovereignty was raised by the symbolic serpent, Satan the Devil. It gives the sure hope of destruction of Satan and of relief for mankind. It recounts the origin of Babylon and thus of all false religion in the post-Flood earth, thereby aiding in the identification of Babylon the Great in the book of Revelation.—See BABYLON THE GREAT.

Jesus said that if anyone serves God, that one must worship Him with spirit and truth. (Joh 4:24) The Genesis account sets forth the truth of man’s beginnings and of God’s dealings with him. Since everything recorded in Genesis is true and not mythical, we are able to know the truth about man’s history. We can see that up to the time of the Flood men certainly knew the truth of the Biblical account about Eden, for the garden was there and cherubs were there with the flaming sword at its gate. (Ge 3:24) But those who wanted to go the way of their own desires ignored the facts that were before them. Noah, however, served God according to the way that man was originally created to serve him, according to true history. Although, following the Flood, Nimrod set up rebellion against God at the Tower of Babel, the patriarchs through the line of Shem continued to hold to the true way of life. When it was God’s time to organize Israel into a nation and give them the Law, it did not come to them like something completely unknown, a revolutionary change in their way of life. No, for in the patriarchal society they had done many of the things that are found in the Law. As M’Clintock and Strong’s Cyclopædia (1881, Vol. III, p. 782), declares: “This theocracy cannot have entered into history without preparatory events. The facts which led to the introduction of the theocracy are contained in the accounts of Genesis.”

This, in turn, prepared the way for the Messiah and the introduction of Christianity. When Jesus Christ arrived, those who had been living according to the Law to the best of their ability were soon able to identify him. He did not appear suddenly and announce himself to be a great savior and leader without any background or historical credentials. The background that had been furnished right from Genesis on down enabled the honesthearted ones to recognize and follow him. Therefore a strong organization of Jewish Christians could be established as a nucleus, prepared to bring a convincing gospel message to the nations. The forefathers of the pagan nations had led them away from the truth. They were “alienated from the state of Israel and strangers to the covenants of the promise, and . . . had no hope and were without God in the world.” (Eph 2:12) Therefore, they had to learn the principles of God from the beginning before they could become Christians.

Genesis, then, provides a valuable basis for understanding all the other books of the Bible and is essential to Christianity. It sets the theme for the Bible, namely, the vindication of Jehovah’s sovereignty and the ultimate fulfillment of his purpose for the earth, by means of his Kingdom under the promised Seed. In addition to the very first and basic prophecy at Genesis 3:15, Genesis has within it numerous other prophecies, a great many of which have been fulfilled since its composition.

[Box on page 921]

HIGHLIGHTS OF GENESIS

A record of God’s creating and preparing the earth for human habitation, of mankind’s role in God’s purpose, and of God’s dealings with men of faith during some 2,300 years of early human history

Covers the period from the beginning of the physical creation down to the death of Joseph in Egypt (1657 B.C.E.)

Creation of physical heavens and earth, and the preparation of the earth for human habitation (1:1–2:25)

Sin and death enter world; “seed” foretold as deliverer (3:1–5:5)

Serpent deceives woman; she and Adam partake of forbidden fruit

Serpent, woman, and Adam sentenced; woman’s seed to crush serpent

Cain, firstborn son of Adam and Eve, murders his brother Abel

In fulfillment of God’s judgment, Adam dies at 930 years of age

Wicked angels and men ruin earth; God brings global Flood (5:6–11:9)

Noah is born in line of Adam’s son Seth; in his day disobedient angels marry women and father the Nephilim, who indulge in violence

Jehovah decrees destruction by a deluge but instructs Noah to build an ark for the preservation of his family and basic animal kinds

Floodwaters overwhelm the whole earth; all humans, flying creatures, and land animals outside ark perish

After the Flood, Jehovah prohibits eating blood, authorizes death penalty for murder, and establishes rainbow covenant, promising never to bring another deluge

During the second generation born after the Flood, people begin to build a tower, defying God’s purpose for them to spread abroad; Jehovah confuses their language, scattering them

Jehovah’s dealings with Abraham (11:10–25:26)

Shem’s descendant Abram leaves Ur in obedience to God’s call

In Canaan, Abram is promised that his seed will receive the land

Lot separates from his uncle Abram, settles near Sodom, is taken captive, and afterward is freed by Abram; Melchizedek blesses Abram

Abram takes Hagar as concubine, and she gives birth to Ishmael

Jehovah changes Abram’s name to Abraham, and Sarai’s name to Sarah; covenant of circumcision is established

Jehovah’s angel informs Abraham that Sarah will bear a son—Isaac

Told of judgment upon Sodom, Abraham pleads for the righteous

Angels urge Lot and his family to leave Sodom; Lot’s wife perishes for disobedience

Isaac is born; Ishmael’s taunts at Isaac’s weaning lead to dismissal

In obedience to Jehovah, Abraham attempts to sacrifice Isaac, and he receives assurance respecting the covenant promises

After Sarah’s death, Abraham arranges to get a wife for Isaac

Isaac’s wife Rebekah gives birth to Esau and Jacob

Jacob (Israel) and his 12 sons; to Egypt for the preservation of life (25:27–50:26)

After Jacob had bought the birthright from Esau for a meal and later, at Rebekah’s urging, procured the blessing Isaac intended for Esau, Jacob departs for Paddan-aram, seeking a wife

Rebekah’s brother Laban tricks Jacob into marrying Leah; then Jacob marries Rachel; by Leah and Rachel and their two maidservants, Jacob has 11 sons and a daughter Dinah before leaving Paddan-aram with his family

Jacob wrestles with an angel, and his thigh joint is put out of place; he desperately clings to the angel in order to receive a blessing, and his name is changed to Israel

After a peaceful meeting with Esau, Jacob resides at Succoth and then at Shechem, where Dinah is violated

Rachel dies when giving birth to Jacob’s 12th son, Benjamin

Out of hatred for Joseph, Rachel’s firstborn, his half brothers sell him; he becomes a slave to Potiphar in Egypt

Imprisoned on false charges, Joseph comes into circumstances that bring his ability to interpret dreams to Pharaoh’s attention

Joseph interprets Pharaoh’s dreams regarding a famine and is made second ruler in Egypt

Famine in Canaan forces Jacob’s sons to go to Egypt for food; in time Joseph reveals himself to his half brothers

Jacob and his household move to Egypt; Joseph cares for them


Jacob dies in Egypt after pronouncing prophetic blessings on Joseph’s sons, Ephraim and Manasseh, and on his own 12 sons

Time to bring Russia in from the cold?:Pros and cons.

On Darwinism's two headed coin

Finagling Molecular Clocks to Fit Darwinism
Evolution News & Views

Finagle's Constant is whimsically defined as "that quantity which, when added to, subtracted from, multiplied by, or divided by the answer you got, gives you the answer you should have gotten." One of the best examples in modern science is the so-called "Molecular Clock" hypothesis in evolutionary theory.

In Current Biology, Michael S. Y. Lee and Simon Y. W. Ho teach the uninitiated about the wizardry that goes into molecular clocks. First, a bit of history.

In the 1960s, several groups of scientists, including Emile Zuckerkandl and Linus Pauling, had noted that proteins experience amino acid replacements at a surprisingly consistent rate across very different species. This presumed single, uniform rate of genetic evolution was subsequently described using the term 'molecular clock'. Biologists quickly realised that such a universal pacemaker could be used as a yardstick for measuring the timescale of evolutionary divergences: estimating the rate of amino acid exchanges per unit of time and applying it to protein differences across a range of organisms would allow deduction of the divergence times of their respective lineages.... [Emphasis added]
Remember this: at first, biologists assumed they had discovered a reliable timepiece. Great, they thought; now we can watch Darwin's tree of life unfold over time. This new clock would show the sequence of great transformations: when animals emerged from the sea, when flowering plants blossomed on land, and when the ancestors of great whales began swimming. Unfortunately, as with many things in biology, complications soon set in.

In the 50 years since, leaps in genomic sequencing technology and new computational tools have revealed a more complex and interesting reality: the rates of genetic change vary greatly across the tree of life. The term 'molecular clock' is now used more broadly to refer to a suite of methods and models that assess how rates of genetic evolution vary across the tree of life, and use this information to put an absolute timescale on this tree. Modern molecular clocks are thus critical to inferring evolutionary timescales and understanding the process of genetic change. Analyses of genomic data using clock models that accommodate variation in evolutionary rates have shed new light on the tree of life, as well as the organismal and environmental factors driving genetic change along its branches. However, some major theoretical, empirical and computational challenges remain.
It's not a clock then. It's not reliable. The genetic changes tick at wildly different rates. Ah, but the promise of "shedding light" on evolution was too tempting to let it go. With a few tweaks and new assumptions -- a little finagling -- molecular clocks might still prove useful. We'll just give the variations an impressive-sounding name. How about "rate heterogeneity"?

Modern molecular clocks can handle various forms of evolutionary rate heterogeneity. Rates can vary across different parts of the genome (site effects), across taxa (lineage effects), and across time (here termed 'epoch effects').
Moving along, Ho and Lee engage in some rationalizations for stretching, compressing, and force-fitting wildly different clock rates into Darwin's tree. It's reminiscent of naughty Johnny telling more and more lies to back up the first one.


An extra layer of interest and complexity emerges when two or more sources of rate heterogeneity interact. Site and lineage effects interact when different genes have different patterns of rate variability across taxa (Figure 2D). Mitochondrial DNA has greatly accelerated rates of evolution in snakes and dragon lizards compared with typical lizards, but nuclear DNA shows no such trend. Genomic analyses suggest that such interactions are widespread. Selection might be relaxed on particular genes in particular taxa and thus lead to rapid molecular evolution. For example, the genes coding for tooth enamel are no longer under stabilizing selection in toothless mammals such as anteaters and sloths. Thus, those genes evolve much more rapidly in these lineages, but this pattern is not seen for most other genes. Such complex patterns of rate variation can be accommodated using partitioned clock models, where different portions of the genome are recognized as evolving according to separate clocks or 'pacemakers'.
There is one fixed star that keeps the finaglers on target: the fossil record. It reliably shows the divergence times and patterns over evolutionary history. But wait. Wasn't the molecular clock supposed to be the yardstick for the fossil record? Which clock is calibrating which?

Molecular clocks are vital to reconstructing the detailed timescale and branching pattern of the tree of life, especially in soft-bodied groups that have left few or no fossils. In turn, this can shed light on how major evolutionary events have been influenced by Earth history. However, the use of inappropriate clock models or erroneous calibrations can produce highly misleading estimates of evolutionary timescales. These issues have led to vigorous debates about the timing and drivers of major evolutionary events, including the origins of animal phyla, the ordinal divergences of birds and mammals or the radiation of flowering plants.
The "origins of animal phyla" -- this brings them to the Cambrian explosion. As an example of many spectacular differences between molecular clocks and fossil-record clocks, Ho and Lee point to molecular estimates that put the emergence of animal phyla "a billion years ago -- nearly twice the age of the explosion of animal fossils in Cambrian rocks." Now what to do? Evolutionists tried to compress the rates as far as they could, but it wasn't enough.

These results were at least partly driven by failure to account for lineage effects: genetic change generally occurs more slowly in vertebrates than in invertebrates, but early molecular analyses extrapolated the slow vertebrate evolutionary rate across the entire animal tree. This caused the estimates of animal divergence times to be stretched deep into the Precambrian. Subsequent analyses with better models of rate variation and more carefully chosen calibrations moved the initial radiation of animals to a later time -- into the early Ediacaran period, when the world was gripped by several massive glaciation events ('snowball earth'). Nevertheless, this still precedes the first definitive metazoan fossils by tens of millions of years.
One pattern does emerge; molecular divergence times are generally older than fossil divergence times. But with flexible clocks, how can one know which to rely on? The situation resembles the folk tale about the town crier who set his watch by the church bell, only to find out the bell ringer calibrated his tolling by the town crier's call.

The fixed star on which both methods rely is actually neither one: it is the assumption of Darwin's tree of life. With that in mind, watch this:

One intriguing but largely untested suggestion is that molecular evolution might occur much more rapidly during evolutionary radiations, leading to big genetic divergences in short time intervals. This would be likely to cause current clock models to overestimate divergence ages.... The link between higher rates of evolution and evolutionary success might prove to be more general, and relevant for phenotypic as well as genetic traits.
Mr. slow-and-gradual Darwin might be scandalized by the notion that evolution could be rapid, but he would be gratified to know that finagling a few assumptions can leave his tree intact.

In sum, what we were told would provide empirical evidence for evolution actually has morphed into a set of assumptions and methods to calculate different Finagle's Constants for each part of Darwin's tree, in order to keep the picture from getting falsified. Empiricism must yield to that requirement.

Lee and Ho end by saying, "we can choose to identify and analyse only the genes that display the most desirable of evolutionary timescales." On the other hand, "Instead, more room for improvement might lie in developing better models of rate variation and refining our knowledge and use of calibrations." Each animal, each lineage, each gene, and each epoch are now going to need their own calibration method, based on what is needed to keep the Tree of Life from falling. "For these reasons, molecular clocks will continue to play a key role in shaping our understanding of the evolution of life and the genes that code for it."

For more on problems with the molecular clock hypothesis, see here on the Cambrian explosion, Casey Luskin on placental mammals and biogeography, and Stephen Meyer's analysis of "lightning-fast evolution" to explain the Cambrian enigma.

Descartes should have thought again?

Descartes’s Blunder
Michael Egnor

What is it that we are most sure of? It’s a fundamental question, the object of philosophical analysis for millennia. Our modern answer to this question was provided by René Descartes in the 17th century. Descartes’s answer is the answer most modern men would give. But Descartes got it wrong.

Descartes set out to rethink metaphysics from the ground up. In Meditations on First Philosophy, he asked this question: How do I know what is real? Of what can I be certain? He suggested this scenario: Imagine that his mind is controlled by an evil demon. The demon is of “upmost power and cunning [and] has employed all his energies in order to deceive me.” How, he asked, could he know whether or not this were the case? Descartes doubted the reliability of his senses: they can deceive, he believed. Of what can he really be certain?

He concludes, famously, that he can be certain only of this: that he exists. Cogito ergo sum. Because even to doubt his own existence presupposes his existence.

This metaphysic of radical skepticism forms the basis for much of Descartes’s metaphysics, which we moderns have (largely unconsciously) inherited.

But Descartes is misguided (and not by a demon). Most fundamentally, he is wrong about the thing that we are most sure of.

The foundation of epistemology is not self-awareness. This can be understood by considering Descartes’s maxim, “Cogito ergo sum.” Notice that we cannot conclude that we exist unless we can conclude. That is, we must first know the principle of non-contradiction — that being is not non-being — before we can conclude that “I think therefore I am.”

“Therefore,” not “I think” nor “I am,” is the crux of the most important thing we know. The principle of non-contradiction is prior to self-awareness.

This is a foundation of Thomistic philosophy. St. Thomas notes:

By nature our intellect knows being and the immediate characteristic of being as being, out of which knowledge arises the understanding of first principles, of the principle, say, that affirmation and denial cannot coexist (opposition between being and non-being) …

(Summa Contra Gentiles: II, 83. Cf Ia IIae, q. 94, a.2.)
Aquinas derives his principle from Aristotle’s principle of non-contradiction: a thing cannot be and not be at the same time. It is the most fundamental thing we know, because if we do not know it, even Descartes’s first principle — cogito ergo sum — is not true. If being and not being could coexist, if contradiction were metaphysically possible, then it would be possible for me to think and at the same time not to exist.

The law of non-contradiction, not cogito ergo sum, is the foundation of knowledge.

It’s worth noting that modern atheists and materialists have a particular problem with non-contradiction. Consider a number of atheist and materialist claims in this light.

Materialists and atheists claim that ID is scientifically wrong, and claim that ID is not scientifically testable. But of course, in order to be scientifically wrong, ID must be scientifically testable.

Materialists and atheists believe that our minds evolved by natural selection. But if we evolved wholly by natural selection, we evolved to maximize reproductive success, not to discern truth, and thus we could not trust our belief that we evolved by natural selection.

Materialists and atheists believe that determinism is true and that free will is not real. But if determinism is true and we lack free will, then our opinions are determined by physical processes, which are not propositions and which lack truth value. Chemical reactions are neither true nor false, so a materialist’s opinion that determinism is true and free will is not real has no truth value.

Materialists and atheists believe that the universe spontaneously came from nothing, and they define nothing as the laws of quantum mechanics.

Materialists and atheists believe that the existence of evil disproves the existence of God, yet if there is no ultimate Source of right and wrong, there is no evil and no good; there are merely circumstances we like or dislike. Nietzsche, unlike the New Atheists, understood this.


Again and again, materialists and atheists hold opinions that violate the law of non-contradiction. In this sense, atheism and materialism aren’t even really metaphysical theories. They’re just self-refuting nonsense.

In attempting to explain away molecular motors Darwinists fumble the ball.

Berra’s Blunder in Molecular Motors
Evolution News @DiscoveryCSC

Whenever we see new articles and papers about cellular motors like ATP synthase and the flagellum, we get excited, thinking that now, finally, someone might make a design inference that questions Darwinism. That’s why this from Imperial College London, “How bacteria turbocharged their motors,” raised our hopes:

Bacteria use molecular motors just tens of nanometres wide to spin a tail (or ‘flagellum’) that pushes them through their habitat. Like human-made motors, the structure of these nanoscale machines determines their power and the bacteria’s swimming ability.

Previously, the team from the Department of Life Sciences at Imperial looked at these motors and discovered a key factor that determined how strongly bacteria could swim. Like human-made motors, bacterial motors have distinct ‘stator’ and ‘rotor’ components that spin against each other. 

“Like human-made motors” – great! They see the light. Our hopes were dashed when we discovered that the goal of their research was to vindicate Darwinism:

The team found that the more stator structures the bacterial motor possessed, the larger its turning force, and the stronger the bacterium swam. Despite these differences, DNA sequence analysis shows that the core motors are ancestrally related. This led scientists to question how structure and swimming diversity evolved from the same core design.

OK. But it’s the way that the reporter, Hayley Dunning, explained evolution that was startling. Don’t evolutionists in 2018 know their own theory?

Ranking: Flagella with 12 stators are labeled “primitive” but those with 17 stators are ranked “sophisticated.” These are arbitrary adjectives.
Lamarckism: The article describes parts of the flagellum “fusing” to allow more stators, and thus graduating to “sophisticated” rank. How mutations did that is not described, nor how the accident became heritable.
Saltation: Darwin stressed that “Natural selection … can never take a great and sudden leap, but must advance by short and sure, though slow steps.” Yet this article alleges that flagella suddenly went from primitive to sophisticated versions in one “quantum leap.”
Berra’s Blunder: The article claims that extra structures attached to the “sophisticated” flagella illustrate evolution, reminiscent of how Tim Berra asserted that you can see evolution in action by watching how Corvettes added parts between 1953 and 1955.
Convergence: Observations show some of the extra structures occurring in unrelated species. She attributes this to the magic wand of convergence: “The extra structures appear to have evolved many times in different species of bacteria, using different building blocks but producing the same functionality.” The writer appeals to convergence in wings and eyes as illustrations.
Inevitability and Creativity: Natural selection is supposed to be blind, random and uncaring, but not here!
We’ll let Dr. Morgan Beeby of Imperial College express these blunders in his own words:

Dr. Beeby said: “Bacterial motors are complex machines, but with studies like this we can see how they have evolved in distinct steps.

“Moreover, the ‘leap’ from 12 stators to 17, while a great innovation, has an aspect of ‘biological inevitability’ in the same way as wings, eyes, or nervous systems in higher animals: the precursors of high torque have evolved multiple times, and one set of them ended up fusing to form the scaffold we describe in our work”.

He added: “Evolution is a creative process, often drawing on variations upon a theme. It is constantly churning out new molecular ideas, many of which fail, but inevitably some get realised multiple times. We have seen this in animals, and now we see this process in the nanoscopic world of molecular evolution too.”

Whatever “evolution” Beeby is talking about is surely not Darwin’s variety, or that of neo-Darwinians, either. He has essentially proposed miracles by another name. Does his paper in Nature Scientific Reports do better? He has Bonnie Chaban and Izaak Coleman as co-authors. Will they correct his blunders? Nope. All three embrace the fake Darwinism wholeheartedly. They see design, but attribute it to a “‘quantum leap’ evolutionary event.” They see the addition of new structures the way Berra saw new parts added to intelligently designed automobiles as an illustration of evolution.

One ray of hope breaks through in the middle of the paper, suggesting that ID has penetrated the conscience of these Darwinians, putting them on the defensive:

How did the Campylobacter-type motor evolve from a simpler ancestral motor? During our previous work, we discovered that each accessory protein is essential, posing a conundrum: how could proteins have been added stepwise to form this (naively “irreducibly complex”) motor?

Of course, they do not provide a reference to Darwin’s Black Box, nor define his term irreducible complexity. They don’t deal with co-option problems, genetic codes, or Scott Minnich’s challenges.

But in this backhanded swipe at Michael Behe, calling him naïve, they reveal an awareness that they are playing defense. “To identify a possible incremental evolutionary pathway, we determined a phylogeny…” etc.  Basically, they arrange flagella from different bacterial species the way Berra arranged Corvettes to prove evolution. Their conclusion, however, seems less bombastic than usual: “our structural and phenotypic results enable us to propose a working model for the incremental evolution of the bacterial flagellar motor.” ID is getting under their skin. The callout quote in the news release affirms Darwinism against ID over the loudspeaker:

Bacterial motors are complex machines, but with studies like this we can see how they have evolved in distinct steps.

ATP Synthase

Meanwhile, the other main rotary engine in cells, ATP synthase, has been examined in greater detail than ever before. That is thanks to a cryo-electron microscopy study reported in Nature Communications.

These reconstructions are of higher resolution than any EM map of intact rotary ATPase reported previously, providing a detailed molecular basis for how the rotary ATPase maintains structural integrity of the peripheral stator apparatus, and confirming the existence of a clear proton translocation path from both sides of the membrane.

What does this paper say about evolution? Not much. The Japanese team basically does a lateral pass to other papers for coverage of motor evolution. “Eukaryotic V-ATPases are likely to have evolved from homologous enzymes found in archea and some eubacteria,” they say, with three references to Darwinian papers. The only other mention doesn’t help Darwinians: it refers to “evolutionary conservation of the rotor structure,” once again tossing the ball to another paper.

There’s no mention of phylogeny, ancestry, mutation, natural selection, or any other Darwinian argument. From these papers we can infer that the design argument is having an impact. For one, if there were clear, unambiguous arguments for evolution, scientists would proudly present the evidence for it. For another, they wouldn’t offer indefensible notions like this one from Morgan Beeby:

“We are used to observing evolution at the scale of animals or plants, such as the giraffe’s neck slowly getting longer over time to reach previously inaccessible food.

“However, the evolution at the molecular scale is much more radical. It’s like a giraffe having children with necks suddenly a metre longer.”

Another hopeful sign is that scientists increasingly toss the ball to others to explain how things evolved, rather than try to describe it themselves in a rigorous way. Instead, they seem to focus on the molecular machines’ complexity and efficiency, without Darwinian gloss.


Finally, the occasional back-handed swipes by Darwinians directed against ID concepts, coupled with exasperated attempts to provide stepwise evolutionary models, suggests that intelligent design has not, in fact, escaped their notice. They know, like aging athletes relying on reputation alone, worrying about declining cheers from the stands, that they are playing defense against a young and vigorous challenger.

On common design v. common descent.

Adam and the Genome and Human-Ape Genetic Similarity
Evolution News @DiscoveryCSC

In Adam and the Genome, Trinity Western University biologist Dennis Venema covers many other subjects besides what you might expect from the book’s title. We have been reviewing this material by the prominent theistic evolutionist and BioLogos author; find the series so far here.

Thus, Venema cites the high degree of genetic similarities between insulin genes in humans and other mammals as evidence for our common ancestry. He writes:

[W]e can see that there is good evidence to support the hypothesis that these two present-day genes come from a common ancestral population in the distant past … What we observe for this short segment is that the gorilla sequence is identical to that of the human except for one letter; the chimpanzee is identical except for three; and the orangutan is identical except for five. As before, this level of identity far exceeds what is needed for functional insulin, and strongly supports the hypothesis that humans share a common ancestral population with great apes. Indeed, the similarities between these sequences make English and West Frisian look like very distant relatives by comparison.

(Adam and the Genome, p. 30)

The obvious answer to this argument is common design — that humans, gorillas, and orangutans were designed based upon a common blueprint. This would explain genetic similarity between humans and other species quite well.

Venema is aware of this objection, and he doesn’t buy it:

Suppose you decided you wanted to design two languages. Would you design them in such a way that they appear to be closely related to each other, especially if your prowess as a designer is such that you can effortlessly design languages in any way you wish? Furthermore, as a designer, you understand that there are many possible ways to design words, grammar, syntax, and so on. Would you make it appear that your two languages are related to each other, if indeed you wanted to convince others that they were separate, independent creations? (p. 32)

There he goes again, telling God what he can and cannot do. It’s a bit of chutzpah, don’t you think? He’s also telling God what God must intend when he does certain things. In particular, Venema is telling God that if he designs two species to be similar then God must thereby intend to tell us that those species are related through common ancestry. And if those species aren’t really related, then Venema tells God that he is being deceitful.

But what if Venema is putting thoughts into God’s head that aren’t there? What if God could have entirely different purposes for designing two species as similar — purposes that have nothing to do with trying to communicate some message to humans about relatedness or unrelatedness?

The reality is that this is not a theological question. There are good logical reasons why different species may have similar genetic sequences: namely, functional requirements. Those requirements have nothing to do with common ancestry. Engineers know from much experience that there are good ways to design things and bad ways. If you want your design to work a certain way, and you find a good blueprint that accomplishes what you seek, then it’s a good design principle to use that blueprint over and over again. That could easily explain why we see similarities in different species — common design to meet functional requirements.

Even Francis Collins acknowledges the merits of this argument, stating:

Some of that evidence is shown in Table 5.1, where the similarity between the genomes of ourselves and other organisms is displayed. This evidence alone does not, of course, prove a common ancestor; from a creationist perspective, such similarities could simply demonstrate that God used successful design principles over and over again.

(The Language of God, p. 134)

Though Collins of course thinks that common ancestry is a better explanation, his point here is exactly right. Reusing successful designs (like reusing genetic sequences) is a completely valid explanation for why genetic similarities exist between humans and other species.

Like many evolution proponents, Venema is thinking inside an evolutionary box. The similarities he observes may boil down to common design, but he apparently can’t see that. Whether we humans properly interpret or misinterpret the meaning of those similarities need not be God’s concern.

Venema’s points here ultimately seem to be rhetorical, though. He writes: “No matter how you slice it, the human and chimpanzee genomes are nearly identical to one another.” (p. 32) This is supposed to impress the reader, leaving no alternative but to conclude that humans and chimps must be related. Venema admits that by some metrics the human and chimp genomes are only 95 percent similar. Fine. But the exact number really isn’t important. What is the metric for demonstrating common ancestry based upon genetic similarity? There doesn’t seem to be one. Venema’s argument appears arbitrary.


Moreover, others geneticists have argued that human-ape genetic similarity might be significantly lower than 90 percent. See,  Human/Ape Common Ancestry: Following the Evidence.” See also, “Critically Analyzing the Argument from Human/Chimpanzee Genetic Similarity.” Perhaps the best treatment of the issue of human-chimp genetic similarity, however, is the chapter “Genetic Evidence for Human Uniqueness,” by Ann Gauger, Ola Hössjer, and Colin Reeves in the book Theistic Evolution: A Scientific, Philosophical, and Theological Critique. We recommend it to Dr. Venema.