Vaccines Don't Cause Autism

 
David Kirby is one of the most prominent proponents of the claim that autism is really mercury poisoning and it's caused by childhood vaccines. This isn't my field but I can recognize woo when I see it. Fortunately for the side of rationality, there are some smart people who know how to deal with the purveyors of ignorance. One of these is Orac at Respectful Insolence.

The US government recently settled a court case that appears to concede a role for vaccines in autism. Orac dissects that claim in a really excellent posting, David Kirby and the government "concession that vaccines cause autism": The incredible shrinking causation claim. Here's the bottom line ...
Orac is the nom de blog of a humble pseudonymous surgeon/scientist with an ego just big enough to delude himself that someone, somewhere might actually give a rodent's posterior about his miscellaneous verbal meanderings, but just barely small enough to admit to himself that few will. (Continued here, along with a DISCLAIMER that you should read before reading any medical discussions here.)¹

One thing that you should remember about Kirby's pretty rhetorical flourishes and speculation. It's all there to distract you from the utter failure of science to support the original claims of the mercury militia, namely that mercury in vaccines was the cause for most cases of autism, or, as Generation Rescue puts it, that autism is a "misdiagnosis for mercury poisoning." Multiple large and well-designed epidemiological studies have utterly failed to find a link between mercury in vaccines or vaccines in general and autism. Indeed, the idea that vaccines cause autism is the incredible shrinking hypothesis. It's gone from confident claims that mercury or vaccines cause nearly all cases of autism to a lot of handwaving based on one case conceded by the government in which the plaintiff had a rare mitochondrial disease which may have been aggravated by vaccines plus multiple bouts of inflammation due to otitis media, a far cry from previous cries blaming vaccines for an "autism tsunami." Is it possible that in rare cases vaccines can aggravate a preexisting condition and lead to injury that resembles autism or ASD? Despite all the studies cited by Kirby in is speculations, what we really have is one documented case of a child in which childhood vaccines probably exacerbated a preexisting mitochondrial disease who later went on to meet the diagnostic criteria for mild autism; so it's possible. It's also a far cry from the original claims of the mercury militia. Don't forget that. Also don't forget that, no matter what new physiologic alterations or abnormalities are found in autistic children, antivaccinationists always--and I mean always--manage to find a rationale to link it to vaccines, no matter how tortured that rationale is.

This is a serious issue. It's part of a much bigger picture including the attack on science by creationists. The issue is not only science vs. religion: it's rationalism vs. superstition. David Kirby is just as dangerous to the cause of science as Jonathan Wells of any or the other creationists.

Other Links: Rebecca on Skepchick: Vaccines don’t cause autism. Okay?

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1. This is one of those times when I refer to an anonymous blogger because, as Orac himself admits, his identity is an open secret.

Hybrid Plants Colonize New Environments

 
Today's Botany Photo of the Day shows Helianthus anomalus, a hybrid species of sunflower that grows in the sand dunes of Utah.

This species arose about 50,000 years ago as a hybrid of Helianthus annuus and Helianthus petiolaris. The Botany Photo of the Day website describes experiments that reproduced this hybridization event showing that hybrids can be more fit—in certain environments—than either parent. [see Jane Harris Zsovan Doesn't Understand Speciation]

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To My American Friends

 
Be careful. here's a great deal at stake here.

The world can't afford another eight years of the Bush doctrine.

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Lunch with the Winners

 
I just got back from lunch with the winners of the Monday Molecule/Nobel Laureate quiz. The two winners were Alex Ling and Dave Schuller. Alex is a student at the University of Toronto. Unfortunately he had to rush off to a class before I could get my camera ready. Maybe I can borrow the photo that Dave took and post it later on.

Dave Schuller is an X-ray crystallographer from Cornell working in the group that manages the synchrotron [MacCHESS]. He decided to drive up from Cornell this morning to have lunch with us. Right now he's on his way back with a stop at McMaster University in Hamilton. Maybe that's why he looks a little dazed in the picture.  

Dave brought me a mastodon from the Natural History Museum at Cornell. He also brought me some Bible Flash Cards so I can practice memorizing my Bible Stories. Here's an example ....

Q: Where did God ask Abraham to go?
A: Isreal, but it took 25 years of traveling to get there.

Some of the other questions were much more difficult. How many of you can remember how Ruth cared for Naomi or where the Last Supper was held? I didn't know the answer to those ones but thanks to Dave Schuller I do now.

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Tangled Bank #100

 
The latest issue of Tangled Bank is #100. It's hosted at AECHAEOPORN [Tangled Bank #100, Bad Flu Edition].

PZ Myers, in his link to this clears up a numbering error, and it turns out this is the 100th edition of Tangled Bank. Congratulation to Dr. Myers in such a long term and well run blog carnival, and thanks to all the other hosts who put time and energy to 1 through 99!

I’ve come down with a terrible flu right in time for Tangled Bank #100. This is making it quite difficult to even sit at my computer and type. Luckily, we have a volunteer to put together this issue in my absence. A famous movie star and producer and great mind of evolutionary biology. His most recent work will include the likes of Dr. Richard Dawkins and Dr. PZ Myers.

Because of various publicity concerns, he wishes to remain nameless. However, he promised that his work will be fair an unbiased, offering no cherry picking or quote mining at all.

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If you want to submit an article to Tangled Bank send an email message to host@tangledbank.net. Be sure to include the words "Tangled Bank" in the subject line. Remember that this carnival only accepts one submission per week from each blogger. For some of you that's going to be a serious problem. You have to pick your best article on biology.

The Humanist Globe

 
I just found a new website called the The Humanist Globe. It was created by Mark Robinson who I met at the opening of the Centre for Inquiry (Toronto) last year.

Check it out. It's full of all kinds of interesting things.

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The α Helix

 
Monday's molecule #63 is an α helix. This conformation of amino acids was first discovered by Linus Pauling who received the Nobel Prize in 1954, partly for his work on the α helix.

The following description of the α helix is taken from Horton et al. (2006) Principles of Biochemistry.

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Figure 4.10
α Helix. A region of α-helical secondary structure is shown with the N-terminus at the bottom and the C-terminus at the top of the figure. Each carbonyl oxygen forms a hydrogen bond with the amide hydrogen of the fourth residue further toward the C-terminus of the polypeptide chain. The hydrogen bonds are approximately parallel to the long axis of the helix. Note that all the carbonyl groups point toward the C-terminus. In an ideal α helix, equivalent positions recur every 0.54 nm (the pitch of the helix), each amino acid residue advances the helix by 0.15 nm along the long axis of the helix (the rise), and there are 3.6 amino acid residues per turn. In a right-handed helix, the backbone turns in a clockwise direction when viewed along the axis from its N-terminus. If you imagine that the right-handed helix is a spiral staircase, you will be turning to the right as you walk down the staircase.

The α-helical conformation was proposed in 1950 by Linus Pauling and Robert Corey. They considered the dimensions of peptide groups, possible steric constraints, and opportunities for stabilization by formation of hydrogen bonds. Their model accounted for the major repeat observed in the structure of the fibrous protein α-keratin. This repeat of 0.50 to 0.55 nm turned out to be the pitch (the axial distance per turn) of the α helix. Max Perutz added additional support for the structure when he observed a secondary repeating unit of 0.15 nm in the X-ray diffraction pattern of α-keratin. The 0.15 nm repeat corresponds to the rise of the helix (the distance each residue advances the helix along its axis). Perutz also showed that the α helix was present in hemoglobin, confirming that this conformation was present in more complex globular proteins.

In theory, an α helix can be either a right- or a left-handed screw. The α helices found in proteins are almost always right-handed, as shown in Figure 4.10. In an ideal α helix, the pitch is 0.54 nm, the rise is 0.15 nm, and the number of amino acid residues required for one complete turn is 3.6 (i.e., approximately 3 2/3 residues:one carbonyl group, three N—Cα—C units, and one nitrogen). Most α helices are slightly distorted in proteins but they generally have between 3.5 and 3.7 residues per turn.

Within an α helix, each carbonyl oxygen (residue n) of the polypeptide backbone is hydrogen-bonded to the backbone amide hydrogen of the fourth residue further toward the C-terminus (residue n + 4). (The three amino groups at one end of the helix and the three carbonyl groups at the other end lack hydrogenbonding partners within the helix.) Each hydrogen bond closes a loop containing 13 atoms—the carbonyl oxygen, 11 backbone atoms, and the amide hydrogen. This α helix can also be called a 3.6₁₃ helix, based on its pitch and hydrogen-bonded loop size. The hydrogen bonds that stabilize the helix are nearly parallel to the long axis of the helix.

Figure 4.11
View of a right-handed α helix. The blue ribbon indicates the shape of the polypeptide backbone. All the side chains, shown as ball-and-stick models, project outward from the helix axis. This example is from residues Ile-355 (bottom) to Gly-365 (top) of horse liver alcohol dehydrogenase. Some hydrogen atoms are not shown. [PDB 1ADF].

A single intrahelical hydrogen bond would not provide appreciable structural stability but the cumulative effect of many hydrogen bonds within an α helix stabilizes this conformation. Hydrogen bonds between amino acid residues are especially stable in the hydrophobic interior of a protein where water molecules do not enter and therefore cannot compete for hydrogen bonding. In an α helix, all the carbonyl groups point toward the C-terminus. Since each peptide group is polar and all the hydrogen bonds point in the same direction, the entire helix is a dipole with a positive N-terminus and a negative C-terminus.

The side chains of the amino acids in an α helix point outward from the cylinder of the helix (Figure 4.11). The stability of an helix is affected by the identity of the side chains. Some amino acid residues are found in conformations more often than others. For example, alanine has a small, uncharged side chain and fits well into the α-helical conformation. Alanine residues are prevalent in the α helices of all classes of proteins. In contrast, tyrosine and asparagine with their bulky side chains are less common in α helices. Glycine, whose side chain is a single hydrogen atom, destabilizes α-helical structures since rotation around its α-carbon is so unconstrained. For this reason, many helices begin or end with glycine residues. Proline is the least common residue in an α helix because its rigid cyclic side chain disrupts the right-handed helical conformation by occupying space that a neighboring residue of the helix would otherwise occupy. In addition, because it lacks a hydrogen atom on its amide nitrogen, proline cannot fully participate in intrahelical hydrogen bonding. For these reasons, proline residues are found more often at the ends of α helices than in the interior.

Proteins vary in their α-helical content. In some, most of the residues are in helices. Other proteins contain very little structure. The average content of helix in the proteins that have been examined is 26%. The length of a helix in a protein can range from about 4 or 5 residues to more than 40, but the average is about 12.

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©Laurence A. Moran and Pearson Prentice Hall

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Horton, H.R., Moran, L.A., Scrimgeour, K.G., perry, M.D. and Rawn, J.D. (2006) Principles of Biochemisty. Pearson/Prentice Hall, Upper Saddle River N.J. (USA)

Nobel Laureate: Linus Pauling

 

The Nobel Prize in Chemistry 1954.

"for his research into the nature of the chemical bond and its application to the elucidation of the structure of complex substances"


In 1954, Linus Carl Pauling (1901 - 1994) was awarded the Nobel Prize in Chemistry for his work on the nature of chemical bonds and the structures of complex molecules. In the field of biochemistry he is best known for working out the form of the α helix in 1948 (published in 1950). The α helix is a stretch of secondary structure in proteins where the polypeptide chain forms a helix. The theoretical model was quickly confirmed by Perutz's group at Cambridge where Francis Crick was working at the time [see The Storyof DNA: Part 1].

The presentation speech was delivered by Professor G. Hägg, member of the Nobel Committee for Chemistry of the Royal Academy of Sciences.
THEME:

Nobel Laureates

Your Majesties, Your Royal Highnesses, Ladies and Gentlemen.

When, in the early nineteenth century, Dalton had produced experimental proofs that matter consists of atoms it was not long before an explanation was sought of the forces that bind the atoms together. Berzelius was of the opinion that this chemical bond was caused by electrostatic attraction between the atoms; according to this belief, a bond was established between two atoms if one of the atoms was positively, and the other negatively charged. In 1819 when Berzelius presented his theory he could apply it almost exclusively to inorganic substances; only few organic substances were known as pure compounds, and the study of these was difficult due to their complicated and often insufficiently known composition. Berzelius, however, contrived to explain, with the help of the new theory, the bond conditions for a great number of inorganic substances, and could in this wav contribute in a high degree to a greater clarity in this field.

Even in inorganic chemistry, however, certain difficulties arose. How should one explain, for instance, how two hydrogen atoms unite to become a hydrogen molecule? In order to obtain attraction between atoms, one of the atoms must be positive and the other negative; but why should two atoms of the same kind possess charges with opposite sign? And when the knowledge of organic compounds increased, new difficulties arose. Berzelius, for example, found it necessary to assume that the hydrogen atom was always positive and the chlorine atom always negative. Now it was also found that in organic molecules a hydrogen atom could often be exchanged for a chlorine atom, which should be impossible if one was positive and the other negative.

With increased knowledge, problems that could not be explained by Berzelius' theory became more and more numerous, and the theory became discredited.

After the atomic theory had been accepted, it soon became apparent that another important object in the field of chemistry must be to determine not only the nature of the chemical bond but also how the atoms are arranged geometrically when they unite to form larger groups, such as molecules. Permit me to quote from a book, remarkable in its day, Die Chemie der Jetztzeit written in 1869 by the Swedish chemist Blomstrand:

"It is the important task of the chemist to imitate faithfully in his own way the elaborate constructions which we call chemical compounds, and in the erection of which the atoms have served as building stones, to determine as to number and relative position the points of attack at which one or the other of the atoms attaches itself to the other, in short, to determine the distribution in space of the atoms."

Blomstrand makes it the aim, therefore, to find the geometrical construction of substances, or what is nowadays called their structure.

At the end of the last century it became obvious that one had to consider several different kinds of chemical bond. Thus, the difficulties of the Berzelius theory were also explained. Berzelius' interpretation was in principle correct as regards a very important type of bond, but he had made the mistake of applying it also to bonds of a different type. After Bohr had introduced his atomic theory one could moreover with its help give a fairly satisfactory explanation of the Berzelius bond. As this bond occurs between electrically charged atoms, so-called ions, this bond type has often been called the ionic bond. The most typical ionic bonds unite the atoms in the crystals of simple salts.

The bond which above all others had prevented a general application of the Berzelius theory is now commonly known as the covalent bond. It occurs commonly when atoms unite to form a molecule and was once characterized by the famous American chemist Gilbert Newton Lewis as "the chemical bond". The bond between the two hydrogen atoms in a hydrogen molecule, which, as was said before, could not be explained by Berzelius' theory, is covalent.

For a long time it was difficult to explain the nature of the covalent bond. Lewis, however, succeeded in 1916 in showing that it is brought about by electrons - generally two - which are shared in common by two neighbouring atoms, thereby uniting them. Eleven years later Heitler and London were able to give a quantum-mechanical explanation of the phenomenon. An exact mathematical treatment of the covalent bond, however, was possible only in the simple case where only one electron unites the two atoms, and when these do not contain additional electrons outside the atomic nuclei. Even for the hydrogen molecule, which contains two electrons, the treatment cannot be absolutely exact, and in still more complicated cases the mathematical difficulties increase rapidly. It has, therefore, been necessary to use approximate methods, and the results depend to a large extent on the choice of suitable methods and the manner of their application.

Linus Pauling has actively contributed towards the development of these methods, and he has applied them with extreme skill. The results have been such as to be easily usable by chemists. Pauling has also eagerly sought to apply his views to a number of structures which have been experimentally determined during the last decades, both in his own laboratory in Pasadena and elsewhere. It is hardly necessary to mention that we have nowadays great possibilities of reaching Blomstrand's objective of determining the distribution of atoms in space. This is principally done by methods of X-ray crystallography involving an examination of how a crystal influences X-rays in certain respects, and then out of the effect seeking to determine how the atoms are placed in the crystal. Pauling's methods have been very successful and have led to observations which have further advanced the theoretical treatment.

But if the structure of a substance is too complicated it may become impossible to make a more direct determination of the structure with X-rays. In such cases it may be possible, from a knowledge of bond types, atomic distances and bond directions, to predict the structure and then examine whether the prediction is supported by the experiments. Pauling has tried this method in his studies of the structure of proteins with which he has been occupied during recent years. To make a direct determination of the structure of a protein by X-ray methods is out of the question for the present, owing to the enormous number of atoms in the molecule. A molecule of the coloured blood constituent hemoglobin, which is a protein, contains for example more than 8,000 atoms.

In the late nineteen thirties Pauling and his colleagues had already begun to determine with X-rays the structure of amino acids and dipeptides, that is to say, compounds of relatively simple structure containing what may be called fragments of proteins. From this were obtained valuable information - about atomic distances and bond directions. These values were supplemented by the determination of the probable limits of variation for distances and directions.

On this basis Pauling deduced some possible structures of the fundamental units in proteins, and the problem was then to examine whether these could explain the X-ray data obtained. It has thus become apparent that one of these structures, the so-called alpha-helix, probably exists in several proteins.

How far Pauling is right in detail still remains to be proved, but he has surely found an important principle in the structure of proteins. His method is sure to prove most productive in continued studies.

It is hardly necessary to question the practical use of the knowledge of the nature of chemical bonds and of the structure of substances. It is obvious that the properties of a substance must largely depend on the strength with which its atoms are united and the nature of the resulting structure. This I does not only apply to the physical properties of the substance, for instance hardness and melting point, but also to its chemical properties, that is to say how it participates in chemical reactions. If we know how certain atoms or groups of atoms are placed in a molecule we can often predict how the molecule should react under given conditions. And as every reaction results in the breaking of some bonds and the formation of others the result will largely depend on the relative strength of the different bonds.

Professor Pauling. Since you began your scientific career more than thirty years ago you have covered a diversity of subjects ranging over wide fields of chemistry, physics, and even medicine. It has been said of you that you have chosen to live "on the frontiers of science" and we chemists are keenly aware of the influence and the stimulative effect of your pioneer work.

Wide though your field of activity may be, you have devoted the greater part of your energy to the study of the nature of the chemical bond and the determination of the structure of molecules and crystals.

It is with great satisfaction, therefore, that the Royal Swedish Academy of Sciences has decided to award to you this year's Nobel Prize for Chemistry for your brilliant achievements in this fundamental field of chemistry.

On behalf of the Academy I wish to extend to you our heartiest congratulations, and now ask you to receive from the hands of His Majesty the King, the Nobel Prize for Chemistry for the year 1954.

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Defining Evolution

 
PZ Myers has started a thread on the definition of evolution [An exercise for the readers]. Here is PZ's choice ...

Evolution is a well-confirmed process of biological change that produces diversity and coherent functionality by a variety of natural mechanisms.

And here's what I posted in the comments on his blog.

The minimal definition of evolution is ..

Evolution is a process that results in heritable changes in a population spread over many generations. [What Is Evolution?]

The truly shocking thing is how many believers in evolution get it wrong. Unfortunately, that includes you PZ. Two of the absolutely essential features of any definition of evolution are: (1) it requires permanent genetic changes and (2) it is populations, not individuals, that evolve. Both of these restrictions are missing from your definition.

What this means is that there are lots of things covered by your definition that do not fit into the scientific definition of evolution. I'll leave it to your readers to come up with a list of such changes.

This is always an interesting discussion and the comments on Pharyngula make some good points. What do Sandwalk readers think of my definition?

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THE SECULAR CONSCIENCE: Why Belief Belongs in Public Life

 
The Centre for Inquiry Ontario is sponsoring a talk by Austin Dacey (photo below) on Friday night March 7th at the Beverley St. location [THE SECULAR CONSCIENCE: Why Belief Belongs in Public Life]. The talk starts at 7:30 pm and there's a reception for Friends of the Centre at 6pm.

I don't like the sound of this. It could be an interesting night.

Austin Dacey, Center for Inquiry's representative to the United Nations will speak in Toronto as one of the first stops on his book release tour.

Secularism has lost its soul. From Washington to the Vatican to Tehran, religion is a public matter as never before, and secular values-personal autonomy, toleration, separation of religion and state, and freedom of conscience-are attacked on all sides and defended by few. The godly claim a monopoly on the language of morality in public debate, while secular liberals stand accused of standing for nothing. Secular liberals have undone themselves. For generations, too many have insisted that questions of conscience-religion, ethics, and values-are "private matters" that have no place in public debate. Ironically, this ideology prevents them from subjecting religion to due scrutiny when it encroaches on individual rights, and from unabashedly advocating their own moral vision in politics for fear of "imposing" their beliefs on others.

In this incisive book, philosopher Austin Dacey calls for a bold rethinking of the nature of conscience and its role in public life. Inspired by an earlier liberal tradition he traces to Spinoza and John Stuart Mill, Dacey urges liberals to lift their self-imposed gag order and
defend a renewed secularism based on the objective moral value of conscience. He likens conscience to the free press in an open society: it is protected from coercion and control, not because it is private, but because it has a vital role in the public sphere. Conscience is free, but not liberated from shared standards of truth and right.

The Secular Conscience will be published by Prometheus Books in March 2008. In spring 2008, the author will bring his timely message directly to secularists, humanists, and skeptics. One of his first stops will be at the Centre for Inquiry Ontario in Toronto.

Austin Dacey, Ph.D., is a philosopher with the Center for Inquiry in New York City, where he serves as United Nations representative and a contributing editor at Skeptical Inquirer and Free Inquiry magazines. He teaches philosophy, ethics, and science education at Polytechnic University and State University of New York. He is the author of articles in numerous publications including the New York Times. His website is www.austindacey.com.

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[Photo Credit: austindacey.com]

Why the Right People Hate IDiots

 
Jonathan Wells (see photo) is one of the leading intelligent design creationists. (As we'll see, that says a lot about the intellectual vacuum that characterizes that cult.)

Wells is best known as the author of Icons of Evolution, a book that makes a virtue out of lying for Jesus (and for Reverend Sun Myung Moon). Almost everything that Wells writes about is demonstrably wrong but that never seems to stop him. He should be an embarrassment to the intelligent design creationist cult except that the members of that cult are all incapable of separating fact from fiction when it comes to science. I've posted previously about two of Well's most egregious falsehoods in Icons because we dissected them in a course I taught last semester [Peppered Moths and the Confused IDiots; Fossil Horses and Directed Evolution].

Recently (Feb. 29) Wells posted an article about the evolution of antibiotic resistance in bacteria and claimed that the authors (Maurice et al. 2008) did not make use of evolution in their study [The Irrelevance of Darwinian Evolution to Antibiotic Resistance]. Here's what Wells said about the work from Dardel's lab.

Third, Dardel and his colleagues made their discovery using protein crystallography. They were not guided by Darwinian evolutionary theory; in fact, they had no need of that hypothesis.

When I first saw the Wells article I seriously wondered whether Jonathan Wells was mentally stable. It looks like he has become completely unhinged since the point of his article is so far from the truth that even a kindergarten student can recognize the lies. (Not surprisingly, the other intelligent design creationists were completely sucked into the lie.)

Ian Musgrave was the first one to hold his nose and post a rebuttal of the Wells article [How stupid do they think we are?]. Somebody had to do it—thanks Ian for doing the research. Your title says it all.

Now, here's the best part. The senior author of the study, Frederic Dardel, posted a comment on The Panda's Thumb website [Frederic Dardel comment]. Here's what Dardel said ...

As principal investigator of the study under discussion, I’d like to strongly support the view advocated this page. In fact, I was completely amazed to see how our work has been misrepresented by M. Wells.

Actually, we did indeed use darwinian evolution within this work (something unusual in structural biology). In order to obtain an enzyme with increased stability (a critical point for structural studies), we used selective pressure to obtain mutants of the enzyme. We selected for bateria with increased aminiglycoside resistance, by plating them on antibiotic containing medium. It turned out that some bacteria evolved such stabler enzymes variants which made this whole study possible !

Finally, I would not consider myself as a chemist, I got my PhD in molecular microbiology. It seems that M. Wells finds it easier to portray us as non-biologists, and hence implicitly as non-evolutionists.

Delicious. PZ Myers picked up on this and posted an article with the title Wells says something stupid again. Of course he did, that's why we call them IDiots.

Now, in light of this you might expect Jonathan Wells to apologize and admit he was wrong. Hands up all those who think he'll do the honorable thing.

WRONG! You guys just don't understand the creationist mentality. Here's how it works, quoting today's posting on Evolution News & Views [Being Hated by the Right People].

As Johnny Cash reputedly once said, “It’s good to know who hates you, and it’s good to be hated by the right people.”

Darwinist bloggers P. Z. Myers and Ian Musgrave hate me. In fact, Myers writes, “My animus for Jonathan Wells knows no bounds.” Well, at least he (unlike Musgrave) spells my name right.

The most recent outbursts by Myers and Musgrave were provoked by my February 29 blog on Evolution News & Views, in which I predicted that Darwinists would try to take credit for a recent French discovery regarding antibiotic resistance. And indeed they did.

In the course of claiming credit for Darwinism, Musgrave claims that I completely misrepresent evolution, molecular biology, genetics and history. Wow. At least I get points for comprehensiveness. As proof of my misrepresentations, Musgrave cites Wikipedia, which everyone involved in this controversy knows is about as balanced and reliable on this issue as P.Z. Myers’s Pharyngula or The National Center for Science Miseducation’s Panda’s Thumb.

....

The principal researcher in the French study disagrees, and wrote to Musgrave’s blog that "we did indeed use Darwinian evolution within this work (something unusual in structural biology). In order to obtain an enzyme with increased stability (a critical point for structural studies), we used selective pressure to obtain mutants of the enzyme."

So the researchers used artificial selection to good advantage. But artificial selection is not Darwinism. People were using artificial selection for centuries before Darwin came along, and they didn’t need Darwin to explain it to them. Darwin argued that an analogous process also operates in natural populations – and so it does. But he and his devoted followers went much further and claimed that it also explains the origin of new species, organs and body plans, which it doesn’t.

You just can't make this stuff up. Wells is an IDiot. I intensely dislike Wells and the lying tactics he uses to promote his cult of intelligent design creationism. I hope that puts me among the "right people."

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[Photo Credit: Evolution News & Views]

Maurice, F., Broutin, I., Podglajen, I., Benas, P., Collatz, E. and Dardel, F. (2008) Enzyme structural plasticity and the emergence of broad-spectrum antibiotic resistance. EMBO Rep. 2008 Feb 22 [Epub ahead of print] [PubMed]

Mendel's Garden #24

 
The 24th edition of Mendel's Garden has just been posted on Bayblab [Mendel's Garden #24 - March 2008].

March has roared in like a lion; the freezing rain here may not be great for venturing outdoors, but it's perfect for a virtual walk through Mendel's Garden, your monthly carnival of genetics. Welcome to the 24th edition.

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Ten Things Everyone Should Know About Science

 
SciBarCamp is starting in less than two weeks.

In the tradition of BarCamps, otherwise known as "unconferences", (see BarCamp.org for more information), the program is decided by the participants at the beginning of the meeting, in the opening reception. Presentations and discussion topics can be proposed here or on the opening night. SciBarCamp will require active participation; while not everybody will present or lead a discussion, everybody will be expected to contribute substantially - this will help make it a really creative event.

Eva Amsen has suggested an interesting topic Ten Things Everyone Should Know About Science. Here's my quick list to get the discussion going ...

1. Science must adhere to methodological naturalism. Supernatural explanations are not allowed in science.


2. All scientific models and theories are provisional in the sense that they might be overturned tomorrow. This does not mean that there's a high probability that well-established theories are wrong. It only means that nothing is absolutely proven in science.


3. Scientists must be skeptics. They must weigh all new data in the light of their current understanding of science. New data must not be accepted unquestionably.


4. Scientists must never lie about science or deliberately misrepresent it to the general public. No exceptions are allowed, even if a little white lying might be for the common good.


5. Scientists must never be afraid to criticize other scientists and they must have the freedom to do so without suffering retribution or penalties. Real science only thrives in an atmosphere of freedom of speech.


6. Theories are the best thing we have in science. A theory is a general explanation of particular phenomena that has withstood many attempts to disprove it. Because of the evidence supporting the explanation and because it hasn't been refuted, a theory will be widely accepted as provisionally correct within the science community.


7. Science is evidence based and the practice of science follows simple rules of logic and rationality.


8. Scientific facts must be reproducible or capable of independent confirmation by other scientists.


9. Science is a way of knowing about the universe. It may be the only epistemologically valid way of knowing. Technology is not the same as science and medicine is not the same as science.


10. There is no such thing as a rigidly defined scientific method.

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Don't Throw the Baby Out with the Bathwater

 
This summer, a number of people, including scientists and philosophers, will gather at the Konrad Lorenz Institute in Altenberg, Austria to talk about evolution. There will be 16 of them and the theme of the meeting is to develop a new theory of evolution. You can read about it in an article by Susan Mazur on Scoop [Mazur: Altenberg! The Woodstock of Evolution?].

The meeting is being organized by Massimo Pigliucci and that does not inspire confidence. Several of the other participants have pretty far-out ideas about evolution.

As most of you know, I'm a fan of Stephen Jay Gould and I support a pluralist approach to evolution. The journalist who wrote the article took the time to interview Richard Lewontin (see photo below) and several other prominent evolutionary biologists who were not invited to the meeting. Here's an excerpt from the article that illustrates one the problems with current thinking about evolution.

A central issue in making a new theory of evolution is how large a role natural selection, which has come to mean the weeding out of traits that don't favor survival, gets to play.

Natural selection was only part of Darwin's Origin of Species thinking. Yet through the years most biologists outside of evolutionary biology have mistakenly believed that evolution is natural selection.

A wave of scientists now questions natural selection's relevance, though few will publicly admit it. And with such a fundamental struggle underway, the hurling of slurs such as "looney Marxist hangover", "philosopher" (a scientist who can't get grants anymore), "crackpot", is hardly surprising.

When I asked esteemed Harvard evolutionary geneticist Richard Lewontin in a phone conversation what role natural selection plays in evolution, he said, "Natural selection occurs."

Lewontin thinks it's important to view the living world holistically. He says natural selection is not the only biological force operating on the composition of populations. And whatever the mechanism of passage of information from parent to offspring contributing to your formation, what natural selection addresses is "do you survive?"

If the meeting was only about the role of chance and accident in evolution then it would be a valuable contribution to evolutionary theory. Instead, as the article makes clear, the "New Evolution" will probably focus on the opposite point of view. You can expect to see heavy emphasis on design, epigenetics, evo-devo and on self-organization as a fundamental principle. (I'm surprised Lynn Margulis wasn't invited.)

These are difficult times for evolutionary theory. I firmly believe that new points of view have to be incorporated into an updated model of evolution. In most cases, these new points of view are not really new—they just haven't been widely accepted by most people who accept evolution. (I'm thinking of things like random genetic drift, punctuated equilibria, modes of speciation, molecular evolution, and our current understanding of how things work at the molecular level.)

Things get complicated because there are other points of view that are trying to capitalize on the current turmoil to push ideas that really lie on the fringe of kookdom. There's a great danger of throwing the baby out with the bathwater. We might end up giving credence to some crazy ideas like Kaufmann's principle of self organization or Kirschner & Gerhart's idea of facilitated variation.

I don't see how most science journalists are going to thread their way through this complicated maze but I admire Suzan Mazur for trying.

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Multicellular Bacteria

PZ Myers posted an article on the evolution of multicellularity [The choanoflagellate genome and metazoan evolution]. He begins with ...

What are the key innovations that led to the evolution of multicellularity, and what were their precursors in the single-celled microbial life that existed before the metazoa? We can hypothesize at least two distinct kinds of features that had to have preceded true multicellularity.

The obvious feature is that cells must stick together; specific adhesion molecules must be present that link cells together, that aren't generically sticky and bind the organism to everything. So we need molecules that link cell to cell. Another feature of multicellular animals is that they secrete extracellular matrix, a feltwork of molecules outside the cells to which they can also adhere.

A feature that distinguishes true multicellular animals from colonial organisms is division of labor — cells within the organism specialize and follow different functional roles. This requires cell signaling, in which information beyond simple stickiness is communicated to cells, and signal transduction mechanisms which translate the signals into different patterns of gene activity.

PZ goes on to describe the genes in a single-cell eukaryote that diverged near the base of the animal phylum. The species is a choanoflagellate called Monosiga brevicollis.

It's important to note that this single-cell organism and its multicellular animal relatives form a distinct clade that is separated from the fungi and plants. Since there are multicellular fungi and multicellular plants, the evolution of multicellularity must have occurred many times.

PZ notes that choanoflagellates have primitive forms of adhesion molecules—one of the prerequisites for multicellularity in animals—but they lack some of the standard animal signalling pathways.

PZ Myers is a fan of evo-devo. There are many problems with this approach to biology but one of the most irksome is the emphasis on animals as models for all of evolution and development. I've referred to this as Animal Chauvinism. In his recent posting PZ is careful not to claim that the evolution of multicellularity in animals is the model for all forms of multicellular species but unsophisticated readers might easily get the wrong impression. Let's try and make the generalization that PZ might have wanted to make.

We can agree with his statement that two requirements of multicellularity are the ability of cells to stick together and the division of labor where cells differentiate to carry out specialized functions. Lest anyone imagines that these properties were invented by animals—or even by eukaryotes—let's look at some simple multicellular bacteria.

The first example is cyanobacteria. That's a filament of Anabaena sphaerica at the top of this posting. The cells adhere to each other through a common cell wall, forming long multicellular filaments. Other species of cyanobacteria form different groups of cells; for example, Glaucocystis (upper right) has four cells together in a single sheath.

Look carefully at the Anabaena filament. Do you see the fat round cell in the middle of the filament? That's a heterocyst. It's a differentiated cell that has become specialized for nitrogen fixation. All the other cells are capable of photosynthesis but the heterocyst specializes in fixing nitrogen. This species is a bacterial example of a multicellular organism with two types of cells.

The specialization of the heterocyst means that the two types of cells have to communicate. This communication takes place via small pores in the cell wall between the cells in the filament. Signaling involves transfer of small molecules such as ATP and glutamine between the various cells. What this means is that some cynaobacteria meet the two criteria that PZ Myers lays out for the evolution of multicellularity. There's no doubt about the fact that this version of a multicellular organism predates the evolution of metazoa by about 2-3 billion years.

The myxobacteria are dramatic example of multicellular bacteria. That's Chondromyces crocatus shown in the photograph above left.

Under certain conditions the single cells of myxobacteria come together to form fruiting bodies that consist of hundreds of cells. In the most extreme examples, some cells form the stalk, some cells form sprangia and others form spores. These are multicellular bacteria with specialized differentiated cells.

There are many other multicelluar bacteria but these two are sufficient to illustrate the point. Cell differentiation and multicellularity are not inventions of animals. There weren't even invented by eukaryotes. Differentiation and multicellularity were invented by bacteria long before the true eukaryotes ever appeared on this planet.

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[Photo Credits: Anabaena sphaerica from Wikipedia: Glaucocystis from Cyanobacteria slides: Chondromyces crocatus from The Myxobacteria Web page]