SEED Magazine

 
The last issue of SEED magazine was published in June. Since then, I've been scanning the shelves of my local convenience stores looking for the latest informative article by PZ Myers and the latest fuel for complaints about the quality of science journalism.

No luck so far. According to the SEED website ...

We are currently finishing an exciting redesign that will be on press this fall. This will also be our first issue with the new tagline.

This sounds ominous. Is the print version of SEED dead?

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Internet Connection Speed Test

 
I think I have a pretty good internet connection but many of my friends tell they have much faster connections. Here's a site that tests your upload and download speeds: Speedtest.net.

I don't know how reliable these are, but here are my results (avg. of five trials):

          DOWNLOAD:  8290 kbps
          UPLOAD:        8080 kbps

I'm pretty happy with my connection through the University of Toronto. Are there better ones out there?



There's another speed test at InterFrog.com. It gives a difference result for upload speeds.

In the first student labs we ran back in 1987 we downloaded DNA sequence files via a 28.8 kbps modem. That was 22 years ago and the connection speed has only increased about 300×. Doesn't Moore's Law say that the improvement should have been more than 1000-fold?

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Creationist Thinking about Spontaneous Generation

 
It's not surprising to discover that creationists are opposed to the idea that life began by purely natural processes. After all, that's at the heart of the dispute between creationists and scientists.

One of the rhetorical tricks used by creationists is to refer to the origin of life as "spontaneous generation." Why is this a trick? Because the term is most commonly associated with an old-fashioned view of spontaneous generation as a process that occurs regularly when new living things spring into existence. The idea was that the maggots on rotting meat arose spontaneously, for example, without the need for pre-existing life.

This notion was put to rest once-and-for-all by nineteenth century scientists; notably, Louis Pasteur. We all know that spontaneous generation of this sort doesn't happen. The creationists take advantage of this when they talk about abiogenesies—the origin of life. If they can confuse their audience by associating abiogenesis with discredited spontaneous generation, then that's a good thing, as far as they are concerned. They know what they're doing and that's what makes it despicable.

This brings me to Denyse O'Leary, Toronto's own version of IDiot. Last month she posed the following question on her blog: Is accidental origin of life a doctrine that holds back science?.

Accidental origin of life is the basic thesis of origin of life researchers. Life all just somehow sort of happened one day, billions of years ago, under the right conditions – which we may be able to recreate. But there is a constant, ongoing dispute about just what those conditions were.

Here is the problem I have always had with accidental origin of life: It amounts to spontaneous generation. However, banishing the doctrine of spontaneous generation played a key role in modern medicine’s success. If we assume that life forms (for medical purposes, we focus on pathogens) cannot start spontaneously, then they must have been introduced. Hence, we can develop procedures for a sterile operating room or lab.

If life can be spontaneously generated, why isn’t it happening now? Conditions for life today are probably as good as they have ever been, and maybe better. For over 500 million years they have obviously been good for complex life forms, and for billions of years they have been good for simple ones.

You can win a creationist book for the best response to her question.

Well, the results are in and the prize goes to StephenB. Here's part of his response. Presumably, this is the best argument the IDiots have to offer on what science is all about.

The accidental origin of life idea hurts science because it militates against the vital principle of causation, the rational and indispensible standard on which science is based. The first question any researcher asks is this: “How did it happen? or—What caused it? Yet, the concept of spontaneous generation popularizes the idea that physical events can occur without causes—that there need not be a “how”—that they can “just happen.”

Consider the following proposition: Streets don’t just “get wet.” Using the scientific and philosophical principle of causation, we understand that something had to cause the streets to get wet. So, we say that if the streets are wet, then it must be raining, or else someone turned on a fire hydrant, or we look for some other reason. But if, as Darwinists or postmodern cosmologists claim, physical events do not always need causes or necessary conditions, that is, if something really can come from nothing, then streets can indeed just get wet. With this mind set, science is severely compromised. If, indeed, something can appear spontaneously or without a cause, why cannot it happen again somewhere else in some other situation?

In keeping with that point, if one thing can “just happen,” then why cannot anything just happen? Why not everything? Under these circumstances, how could the scientist know which things were caused and which ones were not? Science would become an intellectual madhouse where the impossible is affirmed with confidence and the obvious is dismissed with disdain, which, come to think of it, is not a bad description of Darwinst epistemology. For Darwinists, and for postmodern cosmologists, a universe can pop into existence, life can come from non-life, and, yes, streets could, in principle, just “get wet.” Science cannot survive this irrational mind set indefinitely.

Are there any evolutionists out there who believe that the first living cell just "poofed" into existence without any cause or antecedents? If you believe this then please post a comment below.

If nobody admits to holding such a belief, then how do we account for the fact that the IDiots misunderstand and misrepresent science?

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Next-Generation DNA Sequencing

 
There's a real revolution under way in terms of our ability to collect sequence information. The so-called Next-generation DNA sequencing technology relies on the ability to sequence billions of single DNA molecules simultaneously.

How does it work? I was planning on writing up a blog posting to explain the technology since so many experiments rely on it. I kept putting it off but that turns out to be a good thing 'cause others have explained it much better that I ever could have. Watch this video from Helicos.

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[Hat Tip: ScienceRoll]

Nobel Laureate: Ivan Pavlov

 

The Nobel Prize in Physiology or Medicine 1904

"in recognition of his work on the physiology of digestion, through which knowledge on vital aspects of the subject has been transformed and enlarged"

Ivan Petrovich Pavlov (1849 - 1936) (Иван Петрович Павлов) won the Noble Prize in 1904 for his contribution to understanding the physiology and biochemistry of digestion. Part of his contribution was the discovery that some of the digestion enzymes needed to be activated before they could work in the stomach [Monday's Molecule #133].

Pavlov is famous for his work with dogs. Most people know of his studies on conditioned reflexes where he was able to show that the mere anticipation of food caused dogs to salivate. He is famous as one of the founders of modern psychology but the Nobel Prize was for a different study where he examined the stomach secretions of dogs by redirecting secretory ducts to the exterior where the secretions could be collected and analyzed. Pavlov was actually more of a biochemist than a psychologist!

Pavlov had a large, well-equipped lab with many workers. In that sense he was much more of a professional scientist than many of the other biological scientists of the late nineteenth century. Pasteur was another example. Many others, like Charles Darwin, worked alone and didn't seek out students.

The knowledge gained from his studies on digestion had no practical application in medicine. They simply advanced our understanding of how our bodies work. In presenting the Nobel Prize the presenter, Count K.A.H. Mörner, took pains to make this point clear and to pronounce it a good thing. Science for the sake of knowledge.

One gets the impression that the audience at the award ceremonies needed to hear that.

Here's part of the Presentation Speech that describes Pavlov's contribution.

THEME:
Nobel Laureates

In the early days opinions on the course of digestion were speculations as to what was termed as «cooking» or «grinding» in the stomach etc. So long as the digestive processes could not be observed or investigated directly in the stomach no real knowledge could be obtained. An accident turned physiological research in this field in a direction which has later become very important. In the 1820's a young man sustained a gunshot wound in the stomach and developed a gastric fistula which to some extent permitted the gastric processes to be studied. Observations were carried out on this man by the American physician W. Beaumont. This accidental path of investigation, allowing actual observation of processes taking place in the digestive tract, was later followed by many workers using animals. Technique is an important factor in such experiments and has been perfected in a masterly way by Pavlov, whose animals remain in good health, without any injury to the function of their digestive tract, permitting observation and systematic investigation over an almost unlimited period.

These methods for the study of the physiology of digestion established by Pavlov have been taken up by various physiological institutions, but above all much important work was performed in his own laboratory. From this has followed a far-reaching transformation of our knowledge in this field which has also been enriched by new fundamental facts.

The following may be mentioned as an illustration.

The digestive canal can be influenced in various ways by the nervous system. When we remember that the nervous system can induce not only the secretory processes as well as the movements of various parts of the system, but also can bring such processes to a standstill, that it controls the blood supply to these organs and that sensory nerves arise from them, we can get an idea of the complexity one encounters. The complications become still greater when it is realised that we must take into account not only nervous pathways having their origin in the brain or the spinal cord, but also the sympathetic nervous system, and that we have further to pay attention to the interdependence between the different parts of the digestive system through the nerves, so that variations in the behaviour of one may affect that in other organs.

It is in the nature of things that cognition of the scope and character of the functional interdependence of the nervous system and the digestive organs is of great importance to the knowledge of the physiology of these organs. It is also clear that one can only hope that answers to these complicated questions will advance step by step by much research. In this respect Pavlov has acquired very great merit. He has revealed new points of view and has fruitfully stimulated the solution of these problems, and through his methods has made it possible to reach conclusive analysis of them.

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The images of the Nobel Prize medals are registered trademarks of the Nobel Foundation (© The Nobel Foundation). They are used here, with permission, for educational purposes only.

[Photo Credit: Pasteur [Hulton Archive/Getty Images]

Monday's Molecule #137: Winner

 
This is poliovirus and the Nobel Laureates are John Enders, Thomas Weller, and Frederick Robbins. This week's winner is Frank Schmidt of the University of Missouri.

One of the Nobel Laureates, Frederick Robbins, is a graduate of the University of Missouri.

Frank has generously agreed to donate his free lunch to a hungry, deserving, undergraduate so there may be two winners next week.

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Today's "molecule" is actually several molecules, one of which is shown in a diagram below the electron micrograph. You have enough clues to identify this virus. As soon as you get the right answer it will lead you directly to one or more Nobel Laureates.

The first person to describe the "molecule" and name the Nobel Laureate wins a free lunch. Previous winners are ineligible for six weeks from the time they first won the prize.

There are only three ineligible candidates for this week's reward: Maria Altshuler of the University of Toronto, Philip Johnson of the University of Toronto and Ben Morgan of the University of North Carolina at Chapel Hill.

All of the recent winners are in a position to accept their prize so there haven't been any recent winners who donated the free lunch to a deserving undergraduate. Consequently, I do not have an extra free lunch for a deserving undergraduate so I'm not going to continue to award an additional prize to the first undergraduate student who can accept it. Please indicate in your email message whether you are an undergraduate and whether you can make it for lunch. If you can't make it for lunch then please consider donating it to someone who can in the next round.

THEME:

Nobel Laureates
Send your guess to Sandwalk (sandwalk (at) bioinfo.med.utoronto.ca) and I'll pick the first email message that correctly identifies the molecule(s) and names the Nobel Laureate(s). Note that I'm not going to repeat Nobel Prizes so you might want to check the list of previous Sandwalk postings by clicking on the link in the theme box.

Correct responses will be posted tomorrow.

Comments will be blocked for 24 hours. Comments are now open.

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The Devil Among Us: America's First Witch Hunt

 
Here's a clip from the movie The Devil Among Us: America's First Witch Hunt. It's about the first witches who were executed in the colonies of New Haven and Connecticut in New England. (See: The Hanging of Goodwife Knapp in 1653.)

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The Hanging of Goodwife Knapp in 1653

Roger Knapp was born about 1618 in England and came to New England in the early 1640s. He eventually settled in Fairfield in the colony of New Haven in 1644 (now Connecticut). Not much is known about Roger Knapp except that he is listed as a farmer and an Indian trader.

His wife is known only as "Goodwife" Knapp—a title that’s equivalent to "Mrs." Knapp in modern times. (Sometimes shortened to “Goody”. Women with a higher status in society were referred to as “Mistress.”) In 1653 Goodwife Knapp was accused and convicted of witchcraft and executed by hanging in Try’s field outside the village of Fairfield. (None of the witches executed in New England were burned at the stake.)

Nothing is known of the trial of Goodwife Knapp or what she was accused of. This was right in the middle of the epidemic of witch trials and executions in England and Scotland and the phenomenon naturally made its way to the new colonies. Typically, the witch was accused of associating with the Devil, sometimes intimately. The “evidence” was usually a series of unusual happenings that occurred in the presence of the accused, or strange behavior that was deemed to be inappropriate. In many cases, the accused women seem to be rather more outspoken than others—in other words, they didn’t know their proper place.

Men who were accused of witchcraft were also people who were not satisfied with the status quo.

One of the books put on line by Googel is The Salem Witch Trials: a Reference Guide (by K. David Goss). It recounts the trial of Anne Hibbins who was hanged in 1656.

Anne Hibbins (1656) was censured by Boston church leaders for her contentious behavior in repeatedly accusing a local craftsman of overcharging for his labor. She was furthermore charged with supplanting her husband’s position in dealing with this problem, violating the puritan belief that wives should submit themselves to the leadership of their husbands. For this offense, she was unrepentant. She was removed from membership in the Boston church and found guilty of witchcraft in 1654 after the death of her husband. Although the magistrates denied the initial vedict, a second trial was held before the Massachusetts Great and General Court. Anne Hibbins was convicted a second time of witchcraft and executed in 1656. In his assessment of this tragedy, Governor Thomas Hutchinson, in his "History of Massachusetts," places the blame for this conviction upon the people of Boston who disliked Anne Hibbin’s contentious nature. He wrote that the trial and the condemnation of Anne Hibbins for withcraft was "a most remarkable occurrence in the colony," for he found tha is was her temper and argumentative nature that caused he neighbors to accuse he of being a wtich.

It’s very likely that Goodwife Knapp was hung for the same reasons three years earlier in Fairfield in the New Haven Colony.

The remarkable thing about the Goodwife Knapp execution is not the trial itself but the aftermath. Roger Ludlow, the Deputy Governor of Connecticut, had been fighting on and off for several years with his neighbor Mary Staples (wife of Thomas Staples, also known as Staplies). In 1651 Ludlow won a suit against Mary Staples for slander but this did not put and end to their dispute.

During the trial and imprisonment of Goodwife Knapp, Roger Ludlow and his supporters tried to get her to affirm that Mary Staples was a witch but Knapp refused. Just before the execution, Ludlow claimed that Goodwife Knapp came down the ladder and whispered in his ear that Mary Staples was, indeed, a witch.

Ludlow told this story to his friends, Rev. John Davenport and his wife, and it soon spread to the entire village of Fairfield. Accusing someone of witchcraft was a very serious charge—especially just after Goodwife Knapp had been hanged. When Thomas Staples heard that Ludlow was making these accusations against his wife he filed a defamation suit against Roger Ludlow.

The trail took place in May, 1654. There are several accounts on the internet taken from books that have recently been scanned. The best and most readable is from The Witchcraft Delusion in Colonial Connecticut by John M. Taylor. This is from the trial records and some of the descriptions are quite graphic, particularly the account of the examination of Goodwife Knapp’s body for witch’s teates.

There’s another good account in Witch-Hunting in Seventeenth-Century New England: A Documentary History 1638 ... by David D. Hall.

The role of the Sherwood family in the trial is described in A Changing America: Seen Through One Sherwood Family Line 1634-2006.

The reason for my interest in this trial is that many of my ancestors lived in Fairfield at the time and their names are mentioned in the account. Some of my ancestors were friends of the Staples and defended Mary Staples while others sided with Roger Ludlow. Ludlow lost the case and he left Fairfield the following year (1654), making his way eventually back to England and then to Ireland where he remained for the rest of his life.

By an extraordinary coincidence, my good friend and former best man at my wedding, Charles Beach, is a descendant of Mary Staples and Thomas Staples. Their daughter, Mary Nicol Staples (1630-1677) married John Beach (1623-1677).

My living relatives might be interested in our connections to the trial: here they are.

These are ancestors of Isabelle Hooper Burns (1862-1923) the mother of my maternal grandfather. More specifically, they are direct ancestors of her mother’s mother, Esther Treen (1807-~1891).

Here are the names of people mentioned in the defamation lawsuit. Our direct ancestors are underlined. (Some of these have subsequently been proven to be incorrect = strikeout.)

John Banks (1619-1684), attorney for Thomas Staples. (He is my great⁹-grandfather. Most of the others are from this generation or one generation earlier: great¹⁰)

Witnesses Andrew Ward (1597-1659) and his wife Hester Ward = Hester Sherman (1606-1666).

Witnesses: Goodwife Barlow = Ann Ward (?-1684) and her husband John Barlow (1599-1674)

Witness: Goodwife Sherwood = Mary Onge? second wife of Thomas Sherwood (1586-1655). Thomas' first wife, my ancestor, was Alice Tiler¹ (1585-1635).

Witness: Goodwife Odell (Odill) daughter-in-law of John Odell (1574) and Joan Bingley (1581-1640).

Witness: Mr. Jones is John Jones (1591-1665).

Witness: Goodwife Lockwood is Susan (Susanna) Norman (1616-1661) wife of Robert Lockwood (1600-1658).

Witness: Deborah Lockwood (1636-?), 17 years old at the time of the trial and my great⁹-grandmother. She is the daughter of Robert Lockwood and Susanna Lockwood.

Witness: Thomas Lyon (1621-1690).

Witness: Rebecca (Rebecka) Hull is Rebecca Jones, wife of Cornelius Hull and daughter of John Jones (1591-1665) and Sarah UNKNOWN (1599-1650).

Witness: Thomas Barlow was the second husband of Rose Sherwood, daughter of Thomas Sherwood (1586-1655) and Alice Tiler¹ (1585-1655).

Goodwife Pell is not an ancestor of mine but she has an interesting connection. She is Lucy Pell, wife of Thomas Pell who later founded Pelham, in what is now the Bronx, New York City [The Involvement of Thomas Pell's Family in the Witchcraft Persecution of Goody Knapp].

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1. Usually given as Alice Seabrook but this is almost certainly wrong according to A Changing America: Seen Through One Sherwood Family Line 1634-2006, Volume 1 By Frank P. Sherwood.

The drawing of the hanging of Ann Hibbins and the map of the colonies in 1650 are from the HTY277 website of the University of Maine at Farmington.

More Junk DNA Fallacies

 
BiOpinionated is a blog written by a molecular biologist named Nils Reinton. He tries to see every side of an argument but there are times when this attempt goes astray.

The "debate" over junk DNA is an example. Here's how Nils responed to claims by Ryan Gregory and me that most of our genome is junk [How to have your cake, eat it, and then complain].

First: State that most of our genome is junk.

Second: When more and more promoters, enhancers, repressors and other regulatory elements are discovered, claim that this of course was not included in the definition of “most of the genome”. The perfect excuse because it means you’ll never be wrong.

Last: Complain when the press does not understand that “most of our DNA” actually meant “much of our DNA , but with a lot of exceptions” and that science reporters don’t intuitively know which exceptions these are.

Post written using the zpen in dire agony over extremely poor science communication from the same persons who most eagerly criticize science communication from others.[see the original article for links - LAM]

Oh dear. There's so much wrong with the logic of this posting that I hardly know where to begin.

Nils is mostly upset about a recent posting on Genomicron: The Junk DNA myth strikes again (next up: media hype). This isn't very complicated so let me give you the short version.

Most of our genome is junk. That does not mean that all of our genome is junk and it certainly never meant (among intelligent scientists) that all of our non-coding DNA is junk. Here's a short list of non-coding DNA that is absolutely essential in our genome: all genes that produce functional RNAs instead of proteins; all regulatory sequences including enhancers; sequences that control splicing and other RNA processing events such as capping and polyadenylation; some 5′-leaders and 3′-tails of mRNA; chromatin domain markers (regulatory); scaffold attachment sites (SARs); some recombination hotspots; origins of replication; centromeres; telomeres.

Ryan was complaining about a paper that's about to be published in Molecular Biology and Evolution. The authors say this in their abstract.

Protein-coding sequences make up only about 1% of the mammalian genome. Much of the remaining 99% has been long assumed to be junk DNA, with little or no functional significance.

I agree with Ryan Gregory that this is extremely misleading. It implies that there are legitimate scientists who think that all non-coding DNA is junk. It would be far better to say something like this ...

Genes that encode proteins, and other genes, make up only a few percent of our genome. If you add in all of the other DNA sequences that are known to be essential you still can only account for no more than 5% of our genome. Most of the rest is thought to be junk DNA with no biological function. There are no respectable scientists who think that none of it will ever be shown to have a function but the general consensus among the defenders of junk DNA is that the vast majority of these DNA sequences, consisting mostly of defective transposons and pseudogenes, will turn out to have no function.

The authors of the paper go on to present evidence that about 5.4% of non-coding DNA has a function.

Big deal. That's not much more than what the textbooks have been saying for several decades.

Nils, there's an interesting debate going on about the amount of junk DNA in our genome. You're welcome to participate but please make sure you understand the issue and, please, don't spread false information. When we say that most of our genome is junk that does not mean that some of what we now consider to be junk DNA won't turn out to have a function. We're not that stupid—please don't imply that we are.

What we're saying is that the vast majority of DNA sequence in our genome is junk. I think the amount of junk is going to be >90%. That still leaves room for discovering a function for about twice as much DNA as we already know to be functional.

Get back to me when someone publishes solid evidence that more than 10% of our genome is essential.

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Monday's Molecule #137

 
Today's "molecule" is actually several molecules, one of which is shown in a diagram below the electron micrograph. You have enough clues to identify this virus. As soon as you get the right answer it will lead you directly to one or more Nobel Laureates.

The first person to describe the "molecule" and name the Nobel Laureate wins a free lunch. Previous winners are ineligible for six weeks from the time they first won the prize.

There are only three ineligible candidates for this week's reward: Maria Altshuler of the University of Toronto, Philip Johnson of the University of Toronto and Ben Morgan of the University of North Carolina at Chapel Hill.

All of the recent winners are in a position to accept their prize so there haven't been any recent winners who donated the free lunch to a deserving undergraduate. Consequently, I do not have an extra free lunch for a deserving undergraduate so I'm not going to continue to award an additional prize to the first undergraduate student who can accept it. Please indicate in your email message whether you are an undergraduate and whether you can make it for lunch. If you can't make it for lunch then please consider donating it to someone who can in the next round.

THEME:

Nobel Laureates
Send your guess to Sandwalk (sandwalk (at) bioinfo.med.utoronto.ca) and I'll pick the first email message that correctly identifies the molecule(s) and names the Nobel Laureate(s). Note that I'm not going to repeat Nobel Prizes so you might want to check the list of previous Sandwalk postings by clicking on the link in the theme box.

Correct responses will be posted tomorrow.

Comments will be blocked for 24 hours. Comments are now open.

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The "yuck factor"

 
We live in a society that values change and innovation¹ but some changes are too much to stomach. An example might be the proposal to eliminate pain and suffering in cattle raised in feedlots or chickens confined to huge barns (or cages).

"What's wrong with that?", you might ask. You might think that eliminating feedlots is a good thing, but that's not what's being proposed. Instead, the proposal is to genetically modify animals so they quite literally "feel no pain" (Shriver 2009).

The author of this proposal, Adam Shriver, is a philosopher and the suggestion should be treated as a thought experiment and not as a feat of genetic engineering that's about to be implemented by a major meatpacking company. Shriver is a vegetarian so he's familiar with the main arguments against eating meat.

One of those arguments is that the animals we eat are often raised under inhumane conditions where they suffer pain and psychological stress. If we can genetically eliminate pain and stress, then one of the main arguments against meat eating disappears. The logic is impeccable.

Vegans and vegetarians are not about to throw steaks on the BBQ. That's because the "pain and stress" argument isn't really behind their decision to avoid meat.² There are other, far more important, reasons behind their choice of food. What a thought experiment will do, hopefully, is get rid of illogical arguments and focus more attention on the real ethical questions that divide vegetarians and omnivores.

Which brings us to the "yuck factor." I don't read the journal Neuroethics where the Shriver paper was published. I learned about it in the September 5-11 issue of New Scientist [Pain-free animals could take suffering out of farming]. An editorial in that issue points out that in spite of rationality "... there is something deeply unsettling about an animal engineered to be pain free" [Pain-free animals would not be guilt-free].

Sometimes it's not easy to explain why something is unsettling. This is called the "yuck factor" in the editorial. The yuck factor is not always a reliable indicator of real ethical problem.

Some conservative commentators argue that the yuck factor is a reliable indicator that a moral Rubicon has been crossed. Yet all too often such distaste is irrational and a barrier to progress. Progressive thought often comes from ignoring such reactions and thinking things through logically instead.

The editorial argues that opposition to pain-free animals is not irrational. The "real" debate is whether factory farming is acceptable in the first place. It's perfectly respectable to oppose the development of genetically modified (GM) animals, according to the editors of New Scientist.

Maybe, maybe not, that's not the point. As Shriver points out, if you use the argument of pain and suffering then you are bound by rationality to support GM animals. Taking that argument off the table does not mean that you favor factory farms and meat-eating.

The arguments between vegetarians and omnivores often boil down to arguments based on emotions versus arguments based on rationality. I usually side with rationality (but not always).

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1. Sometimes this causes problems, such as when we get confused about the difference between "change" and "improvement." They are not synonyms.

2. And neither is the "ecology" argument. If we could prove tomorrow that raising free-range cattle on scrubland was more energy-efficient than trying to grow wheat on that same land, it wouldn't convert a single vegetarian.

Shriver, A. (2009) Knocking Out Pain in Livestock: Can Technology Succeed Where Morality has Stalled? Neuroethics published online Aug. 21, 2009 [SpringerLink] [doi: 10.1007/s12152-009-9048-6]

An Entire Generation Is Being Brainwashed

 
Kirk Cameron warns us that an entire generation is being brainwashed. You might be surprised at who gets the blame ...

You'll also be surprised at some of the other claims in this video. Have you ever wondered why we call them IDiots? Here's why ...

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How Bad Papers Get Published in Good Journals

 
Donald Williamson used to be a marine biologist. He has some strange ideas about evolution. He thinks, for example, that the reason why butterflies have distinct larval and adult stages is because they arose from the fusion of two separate species—a larva-like species and a butterfly-like species.

Lots of us have crazy ideas but it's a real challenge to get them published in the peer-reviewed literature, and that's how it should be. The reason why science is so successful as a way of knowing is, in part, because it's dominated by skepticism and a requirement for evidence-based rational thought. The system sometimes impedes the acceptance of real innovative ideas but not for long. What is does do successfully, however, is weed out the kooks. But even that doesn't work all the time.

The Proceedings of the National Academy of Sciences (PNAS) is a prestigious journal that's run by the National Academy of Sciences. Once elected to the academy, members have some special privileges when it comes to publishing in the journal. They can "contribute" one of their own papers, in which case they can have a great deal of influence on choosing reviewers, or they can "communicate" the paper of a friend or colleague, in which case they choose the reviewers and send the reviews to the editor of the journal.

It's easy to see the potential for abuse but the remarkable thing is that the process actually works quite well. The quality of papers "contributed" or "communicated" is, in general, no worse than that of papers published in other front-line journals. Two of my own papers were "contributed by" my former Ph.D. supervisor and the process was a rigorous as any other.

But when the system fails, it fails spectacularly.

Lynn Margulis is a member of the National Academy. She "communicated" a paper by Donald Williamson on his strange idea about butterfly evolution (Williamson 2009). That's when the excrement hit the fan.

The editor of PNAS, Randy Schekman, has announced that the "communicated by" option for members will end in July 2010 [PNAS Nixes Special Privileges for (Most) Papers] The Science article reporting on this change in policy leaves little doubt about what prompted it.

An example of alleged gamesmanship popped up online 28 August in PNAS. Lynn Margulis, the noted biologist at the University of Massachusetts, Amherst, communicated a paper by Donald Williamson, a retired marine biologist in the United Kingdom. In it, Williamson promoted his longheld, intriguing—and, say most other biologists, almost certainly misguided—theory about the origins of caterpillars and butterflies. Current biological theory argues that they were always a single species and that each stage evolved via natural selection. Williamson argues instead that two distinct species (one caterpillar-like, one butterfly-like) somehow fused into a hybrid way back when. One species' sperm must have fertilized the other's eggs, transferring genes laterally across species in a non-Mendelian fashion.

Margulis was unavailable for comment, but Williamson says, "Lynn Margulis is prepared to put her name and reputation on the line" to prove that "genome mergers" occur in evolution, a position his paper supports. He also says he knows that Margulis sent his paper to a half-dozen academy reviewers. Williamson says that he thinks they were all positive reviews, but Margulis told Scientific American last week that she canvassed six or seven reviewers to find the two positive reviews necessary to push the paper through.

Shame on you, Lynn Margulis, You've made some outstanding contributions to biology over the years—endosymbioisis being the best example—but it's time to hang up your hat and retire gracefully. Your latest ideas are totally wacky and your inability to distinguish between science and fantasy—as evidenced in your promotion of the Williamson paper—is an embarrassment to those of us who, for several decades, have been holding you up as an example of a successful and creative scientist.

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Williamson, D.I. (2009) Caterpillars evolved from onychophorans by hybridogenesis. Proc. Natl. Acad. Sci. (USA) Aug 28, 2009 [Epub ahead of print] [PubMed] [doi: 10.1073/pnas.0908357106]

Monday's Molecule #136: Winner!

 
This is the Golgi apparatus. It's responsible for sorting and targeting proteins that have to be secreted or localized to internal vesicles. These proteins are inserted into the lumen of the endoplasmic reticulum (ER) during protein biosynthesis and from there they are partially modified and shuffled off to the Gorgi in small vesicles that bud off the ER and fuse with the membrane stacks shown in the image. While in the Gogi the proteins are further modified and targeted to the cell surface or peroxisomes or lysozomes. They travel to those locations in vesicles that bud off the edges of the Golgi disks.

The Nobel Laureate is Camillo Golgi who discovered the Golgi apparatus over 115 years ago.

This week's winner is Ben Ryan, an undergraduate from the University of North Carolina at Chapel Hill. He's the son of an old friend who's now the Managing Editor of American Scientist. It's scary when you realize that people who you remember as toddlers are now university students who can correctly answer Monday's Molecule. I'm hoping that Ben will be able to visit Toronto and collect his prize. I have stories to tell him that I can't put in writing.

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Today's "molecule" is an easy one in celebration of the start of a new academic year for many university students. Name this structure and provide a very brief description of it's function.

The Nobel Laureate should be obvious.

The first person to describe the "molecule" and name the Nobel Laureate wins a free lunch. Previous winners are ineligible for six weeks from the time they first won the prize.

There are only three ineligible candidates for this week's reward: Markus-Frederik Bohn of the Lehrstuhl für Biotechnik in Erlangen, Germany, Maria Altshuler of the University of Toronto, and Philip Johnson of the University of Toronto.

I have an extra free lunch for a deserving undergraduate so I'm going to continue to award an additional prize to the first undergraduate student who can accept it. Please indicate in your email message whether you are an undergraduate and whether you can make it for lunch.

THEME:

Nobel Laureates
Send your guess to Sandwalk (sandwalk (at) bioinfo.med.utoronto.ca) and I'll pick the first email message that correctly identifies the molecule(s) and names the Nobel Laureate(s). Note that I'm not going to repeat Nobel Prizes so you might want to check the list of previous Sandwalk postings by clicking on the link in the theme box.

Correct responses will be posted tomorrow.

Comments will be blocked for 24 hours. Comments are now open.

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Oct. 28-30: Reserve These Dates!

 

THE GAIRDNER FOUNDATION 50TH
ANNIVERSARY TORONTO SYMPOSIUM:

Wednesday, October 28- Friday, October 30, 2009

WEDNESDAY, OCTOBER 28, 2009

Gairdner 50^th Anniversary Symposium on Stem Cells, Disease Mechanisms and Future Therapies in collaboration with the McEwen Centre for Regenerative Medicine.

Location: Macleod Auditorium, University of Toronto

Time: 9am -12:45pm

Co-Chairs: Dr. Janet Rossant, Sick Kids Hospital, Toronto, ON
Dr. Gordon Keller,Director, McEwen Centre for Regenerative Medicine, UHN, Toronto

Introduction: Dr. John Dirks, President and Scientific Director,
the Gairdner Foundation

9.00-9:30
Shinya Yamanaka, Professor, Department of Stem
Cell Biology, Institute for Frontier Medical Sciences, Kyoto University, Japan

Induction of pluripotency by defined factors

9.30-10:00
Gordon Keller, Director, McEwen Centre for Regenerative Medicine, Toronto, ON.

Directed differentiation of pluripotent stem cells to functional tissues

10.00-10:30
Andras Nagy, Senior Investigator Samuel Lunenfeld Research Institute, and Canada Research Chair in Stem Cells and Regeneration ,Toronto, ON

Transposon-mediated reprogramming provides a powerful exploratory tool for understanding stem cell induction

10.30-10:45 Break

10.45-11:15
Mario Cappechi, Distinguished Professor of Human Genetics and Biology, University of Utah School of Medicine, Salt Lake City, Utah

Stem cells of the intestine

11.15-11:45
Phillip Sharp,Institute Professor, Massachusetts Institute of Technology, Boston MA

The roles of small RNAs in stem cells

11.45-12:15
Samuel Weiss, University of Calgary, AB

Adult neurogenesis and the formation of social memories

12.15-12:45
Oliver Smithies, Excellence Professor of Pathology and Laboratory Medicine, University of North Caroline, Chapel Hill, NC

On being a scientist for 60 years

12.45 Reception

1:15-4:45 - Gairdner Global Health Symposium

Location: Dalla Lana School of Public Health, University of Toronto, 155 College Street, 6^th Floor, Toronto, ON M5T 3M7 Canada,

1:15-1:25

Introduction: Dr. John Dirks, President & Scientific Director, The Gairdner Foundation

Welcome: Dr. Jack Mandel, Director, Dalla Lana School of Public Health, University of Toronto

The Global Health Stage

Chair: Kiyoshi Kurokawa, Professor, National Graduate Institute for Policy Studies, Tokyo

1:25-1:40
Jeff Koplan, Director of Global Health, Emory University

What's global health and why is it important?

1: 40-1:55
Tachi Yamada, President of Global Health Program, Gates Foundation

Innovation and access in global health

1:55-2:10Mark Walport,Director, Wellcome Trust.
Building capacity

2:10-2:25
Peter Singer, Director, McLaughlin-Rotman Centre
for Global Health, University Health Network and University of Toronto

Global health: why Canada should care and what Canada should
do.

2:25-2:45
Discussion

2:45-3:00 Break

The Challenge of Chronic
Disease

Chair:Alan Bernstein, Executive Director, Global HIV Vaccine Enterprise

3:00-3:20
Nubia Munoz, Inaugural Canada Gairdner Global Health award recipient

Burden of cancer associated with infectious agents in developing countries.

3:20-3:35
John Sulston, Cambridge, UK
What is Science for anyway?

3:35 -3:50
Margaret G. McGlynn, President, Merck Vaccines, Merck and Company Inc.
The evolving global vaccine landscape

3:50-4:05 Prabhat Jha, Director, Centre for Global Health Research, University of Toronto
Death and tobacco taxes

4:05-4:20
Richard Peto,Professor of Medical Statistics and Epidemiology, Co-Director, CTSU, Oxford University
Halving adult mortality worldwide

4:20-4:40 Discussion

4:40-4:45 Conclusion

Dr. John Dirks, President and Scientific Director, the Gairdner Foundation

1:30-4:45 -The Cell: An Endless Frontier

Location: Macleod auditorium,
University of Toronto

1:30-1:40 Introduction

1:40-2:00pm
Elizabeth Blackburn, Morris Herzstein Endowed Professor in Biology & Physiology, Department of Biochemistry & Biophysics University of California, San Francisco
How cells - and organisms - respond to perturbing their telomere maintenance

2:00-2:20pm
Ulrich Hartl, Max- Planck Institute for Biochemistry, Martinsried, Germany

The cellular machinery of protein folding: Molecular chaperones in health and disease

2:20-2:40
Avram Hershko, Technion Institute of Technology, Haifa

Roles of ubiquitin-mediated protein degradation in cellular regulation

2:40-2:55 Coffee Break

2:55-3:15pm
Bob Horvitz, David H. Koch Professor of Biology, Massachusetts Institute of Technology, Boston and Investigator, Howard Hughes Medical Institute

Genetic control of programmed cell death in C. elegans

3:15-3:35pm
Victor Ambros,Professor, Department of Molecular Medicine, University of Massachusetts Medical School, Worcester, MA

Small RNAs in every corner of the cell

3:35- 3:55
Gary Ruvkun,Professor of Genetics, Harvard Medical School

A C. elegans endocrine system that couples detection of xenobiotic drugs to regulation of reproduction and longevity

3:55 - 4:15
Robert G. Roeder, Arnold and Mabel Beckman
Professor, Laboratory of Biochemistry and Molecular Biology, Rockefeller University, NY

Transcriptional regulatory mechanisms in animal cells

4:15- 4:35pm Richard Axel, Investigator, Howard Hughes Medical Institute and University Professor, Columbia University, NY
Topic TBA

4:35pm Concluding Remarks

THURSDAY, OCTOBER 29, 2009

7:15 - 9:00am -
Gairdner Industry Breakfast, Unclogging the Pipeline: Rejuvenating drug discovery
Location: MaRS Centre, MaRS Collaboration Centre Auditorium


Moderator:Cal Stiller, Chair, Genome Canada/Bioquest Innovations Inc. /Ontario Institute for Cancer Research and Professor Emeritus, University of Western Ontario; Toronto, ON


Speakers:
Philip Sharp, Institute Professor, Massachusetts Institute of Technology; Cambridge, MA

Corey Goodman, Past President, Biotherapeutics and Bioinnovation Center, Pfizer Inc.; San Francisco, CA
David Baltimore, President Emeritus, Robert Andrews Millikan Professor of Biology, California Institute of Technology; Pasadena, CA

Please RSVP by email tothegairdner@gairdner.org, include the first and last name of the total number of guests attending.

9:00 - 3:00 -2009 Canada Gairdner Recipients' Lectures, The Charles Hollenberg Symposium

Location: JJR Macleod auditorium, University of Toronto

9:00am Dr John Dirks, Welcoming remarks

9:15 -9:45am Dr. Peter Walter, Professor, Department of Biochemistry, University of California, San Francisco Investigator of the Howard Hughes Medical Institute, CA,
Protein homeostasis in health and
disease

9:45-10:15am Dr. Kazutoshi Mori, Professor, Department of Biophysics, Graduate School of Science, Kyoto University, Japan
The unfolded protein response: To
mammals and beyond

10:15-10:30 Coffee Break

10:30-11:00am Dr. Lucy Shapiro, Director, Beckman Center for Molecular and Genetic Medicine,Professor, Developmental Biology, Stanford University School of Medicine, Stanford, CA
The systems architecture of the bacterial cell cycle

11:00-11:30am Dr. Richard Losick, Professor, Microbial Development and Gene Regulation, Harvard University, Cambridge, MA
Developmental biology of a simple organism

11:30-12:00pm Dr. David Sackett, Professor Emeritus, Clinical Epidemiology & Biostatistics, McMaster University, Hamilton, ON
On the tribulations of not performing
randomized trials

12:00-1:00pm Lunch Break

1:00-1:05 John Dirks, Introduction of the Inaugural Canada Gairdner Global Health Award

1:05-1:45 Dr. Nubia Munoz, Emeritus Professor, National Cancer Institute, Bogota, Colombia and Visiting Scientist, Catalan Institute of Oncology, Barcelona
From causality to prevention: the case of cervical cancer

1:45-2:15 Dr. Shinya Yamanka, Professor, Department of Stem Cell Biology, Institute for Frontier Medical Sciences, Kyoto University, Japan
Induction of pluripotency by defined factors

2:15- 2:45 Dr. Sydney Brenner, Distinguished Professor, The Salk Institute, San Diego
Humanity's genes

FRIDAY OCTOBER 30, 2009

8:45-3:00-Gairdner/Nobel and Gairdner Laureate Forums

Location: Convocation Hall, University of Toronto
All sessions will present a moderated panel discussion,
followed by Q&A from the audience.

Friday's events are free but registration is required.
Click here.

8:45-10:15amAttack and Repulsions: Infections and the Immune System

Dr. David Baltimore (Moderator), Robert Andrews Millikan Professor of Biology, California Institute of Technology, CA

Dr. Ralph Steinman, Henry G. Kunkel Professor & Sr. Physician, The Rockefeller University, New York

Dr. Emil Unanue, Paul & Ellen Lacy Professor, Department of Pathology & Immunology, Washington University School of Medicine, St. Louis, MO

Dr. Rolf Zinkernagel, University of Zurich, Zurich, Switzerland


10:30-12:00pm The Metabolome: Food and Fuel for Thought

Dr. Joe Goldstein (Moderator), Julie and Louis A. Beecherl Distinguished Chair in Biomedical Science, Southwestern Medical Center, University of Dallas, TX

Dr. Jeff Friedman, Marilyn M. Simpson Professor, The Rockefeller University, New York

Dr. Tony Pawson, University Professor, Program in Molecular Biology &Cancer, Samuel Lunenfeld Research Institute, Toronto

Dr. Michael Brown, Paul J. Thomas Chair in Medicine, Southwestern Medical Center, University of Texas, Dallas, TX

Dr. Ron Evans, Professor, Salk Institute for Biological Studies, La Jolla California

2:00-3:30pm Cancer: Can New Insights into Biology Yield Better Results?

Dr. Michael Bishop (Moderator) Chancellor, University of California, San Francisco

Dr.Harald zur Hausen, Professor Emeritus, German Cancer Research institute, Heidelberg, Germany

Dr.Dennis Slamon, Chief, Department of Hematology, Oncology, University of California, Los Angeles

Dr. Bob Weinberg, Professor of Biology, Member, Whitehead Institute, MIT, Cambridge, MA

Dr. Barry Marshall, International Research Foundation for Helicobacter and
Intestinal Immunology, Virginia

7:00- 8:30pm
The Personalized Genome: Do I Want to Know?

Dr. Michael Hayden, Director and Senior Scientist, Centre for Molecular Medicine and Therapeutics, University of British Columbia, Vancouver

Dr. Sydney Brenner, Distinguished Professor, The Salk Institute, San Diego

Charles Sabine, Award winning NBC News correspondent and carrier of the gene for Huntington's Disease

If you need more information please contact Sheila Robinson at

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