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Tuesday, June 06, 2023

 

No, Garlic will not Cure COVID.

Garlic extracts are in the news with somewhat breathless headlines ( see here [paywall] and here and here) as the Doherty Institute has reported that garlic extracts are able to prevent influenza and SARS-CoV-2 infection of cells in culture. Unfortunately, the full experimental details are not available, but the effects of garlic extracts on viral infection in isolated cells have been seen before and suggest garlic is unlikely to affect the course of COVID infection.

Garlic extract has been shown to inhibit virus activity previously (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7434784/), and SARS-CoV-2 in particular (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8581659/) 

 However, while these preclinical studies are an essential first step to developing therapies, there is a long way to go before these extracts can be adopted as preventatives or treatments. After all, as I said on Media Watch, many things kill viruses in dishes, including extract of old shoes.

Garlic has been used in medicines for millennia, although evidence that it is actually useful is largely lacking. Garlic’s most prominent components are organic sulfur compounds which give it its distinctive smell. More than thirty sulfur containing compounds are present in garlic along with other potentially active compounds such as lecithin's and flavonoid antioxidants (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7434784/). The organic sulfur compound Allicin is thought to be the primary component responsible for antiviral activity. 

Absorption and metabolism of the active components of garlic extracts may mean that the levels of these compounds may not reach levels that are effective in the body. In the previous In vitro studies, rather high concentrations of extract (https://journal.isv.org.ir/article-1-205-fa.pdf, https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4780135/) and Allicin are required to inhibit viral activity (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8581659/). Furthermore, the cell type used in the in vitro experiments affects the results, with Allicin in human lung cells being less effective against SARS-CoV2 than Vero cells (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8581659/).

Garlic compounds are readily broken down and results suggest they do not enter the body at the levels required to inhibit viral reproduction. (https://academic.oup.com/jn/article/131/3/955S/4687054, https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073756/).
 
There was a suggestion that consuming garlic might help with the gastrointestinal effects of COVID, and possibly lead to faster recovery via effects on the GI tract. While it is quite clear that COVID causes gastrointestinal symptoms, it is less clear if this is due to virus in the GI tract binding to the GI epithelium, virus getting to the GI cells via the blood or due to the systemic effects of the virus. Even if it is due to virus in the GI tract infecting the GI epithelium, it is not clear there would be a high enough concentration in the gut content to stop virus binding. The major issue and really serious effects of COVID is the virus binding in the lungs (and the effects on circulation and the heart), so affecting the GI tract is not likely to have a significant impact on the course or the worst adverse effects of COVID.
Small clinical trials of garlic preparations suggest they may reduce symptoms, but not incidence, of colds and flu. The composition and concentrations of these extracts may not be comparable to the materials tested by the Doherty Institute. A small trial with a fortified garlic extract in hospitalised COVID patients showed no significant effect on the primary measures of infection recovery (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10011030/). 
 
Summary:

Overall, while the results reported by the Doherty Institute are interesting, until clinical trials have been done no claims can be made about the effects of these extracts for the prevention and/or treatment of influenza let alone COVID. With what information we already have, an actual benefit seems highly implausible.

References:

Rouf R, Uddin SJ, Sarker DK, Islam MT, Ali ES, Shilpi JA, Nahar L, Tiralongo E, Sarker SD. Antiviral potential of garlic (Allium sativum) and its organosulfur compounds: A systematic update of pre-clinical and clinical data. Trends Food Sci Technol. 2020 Oct;104:219-234. doi: 10.1016/j.tifs.2020.08.006. Epub 2020 Aug 19. PMID: 32836826; PMCID: PMC7434784. 

Mehrbod P., Amini E., Tavassoti-Kheiri M. Antiviral activity of garlic extract on Influenza virus. Iranian Journal of Virology. 2009;3(1):19–23. 

Chavan RD, Shinde P, Girkar K, Madage R, Chowdhary A. Assessment of Anti-Influenza Activity and Hemagglutination Inhibition of Plumbago indica and Allium sativum Extracts. Pharmacognosy Res. 2016 Apr-Jun;8(2):105-11. doi: 10.4103/0974-8490.172562. PMID: 27034600; PMCID: PMC4780135. 

Mösbauer K, Fritsch VN, Adrian L, Bernhardt J, Gruhlke MCH, Slusarenko AJ, Niemeyer D, Antelmann H. The Effect of Allicin on the Proteome of SARS-CoV-2 Infected Calu-3 Cells. Front Microbiol. 2021 Oct 28;12:746795. doi: 10.3389/fmicb.2021.746795. PMID: 34777295; PMCID: PMC8581659. 

Lawson LD, Hunsaker SM. Allicin Bioavailability and Bioequivalence from Garlic Supplements and Garlic Foods. Nutrients. 2018 Jun 24;10(7):812. doi: 10.3390/nu10070812. PMID: 29937536; PMCID: PMC6073756. 

Harunobu Amagase and others, Intake of Garlic and Its Bioactive Components, The Journal of Nutrition, Volume 131, Issue 3, March 2001, Pages 955S–962S, https://doi.org/10.1093/jn/131.3.955S 

Taghavi MR, Tavanaei Tamanaei T, Oghazian MB, Tavana E, Mollazadeh S, Niloofar P, Oghazian S, Hoseinzadeh A, Hesari A, Ansari Mohseni M, Rezaei S, Haresabadi M. Effectiveness of Fortified Garlic Extract Oral Capsules as Adjuvant Therapy in Hospitalized Patients with Coronavirus Disease 2019: A Triple-Blind Randomized Controlled Clinical Trial. Curr Ther Res Clin Exp. 2023;98:100699. doi: 10.1016/j.curtheres.2023.100699. Epub 2023 Mar 14. PMID: 36998289; PMCID: PMC10011030.

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Tuesday, February 15, 2022

 

No, a recent report has NOT found Graphene in COVID vaccines

 The idea that COVID vaccines contain the nano-particle material graphene is a particular myth that refuses to go away. While graphene has a number of desirable properties in biomedical applications, it is not yet used in vaccines. 

However, a new "report" claims that they have found "graphene" in vials of Pfizer, Moderna and Astra-Zenia COVID vaccines. TL;DR this is nonsense on stilts. Why? let me explain.

As a bit of background, I am a biomedical scientist. I have a lot of expertise in optical microscopy (bright field, fluorescence) and some expertise in electron microscopy. I also have expertise in UV-visible spectroscopy and experience with Nuclear magnetic Resonance and Mass Spectroscopy (although the latter is usually me nodding at my collaborators spectra trying to look intelligent).

With that background, let look at the "report", "Qualitative Evaluation of Inclusions In Moderna, AstraZeneca and Pfizer Covid-19 vaccines.". It uses two techniques to find "graphene" in the vaccines, optical microscopy and Raman spectroscopy.

Optical microscopy:

The problem with optical microscopy is that nano-materials are, well, nano, with sizes typically below the resolution threshold of optical instruments. The "report" says that aliquots of vaccine were placed on "clean" slides, dried, then cover slips placed on them. No details are given on how the slides were cleaned, if the cover-slips were cleaned, and what mounting medium was used. 

Looking at the images I see the typical junk that ends up on slides (even cleaned ones and we use acid washing with ethanol rinses on the slides and cover-slips). Stray fibers and the agglomerations you get from drying complex solutions (particularly with lipids, the lipid nano-particles will aggregate as they dry into little blobs of fat). The "carbon nano-ribbons" (Figure 3.1) are not nano (approximately 7 µm in diameter), and the images in 3.2 are definitely not nano (15 µm across) and are the typical junk that accumulates of slides and cover-slips. 

Figure 3.7 from the report, this is the typical non-nano junk every optical microscopist is familiar with.  

These random blobs and fibers are all (aside for some described as calcite) described as graphene with out any good evidence.  Which brings me to Raman spectroscopy.

 

Raman Spectroscopy:

Spectroscopy of any sort of complex mixtures, like vaccines, is fraught with difficulties. Multiple components can interfere with each other and you can find peaks where you don't expect peaks. The "report" shows numerous Raman spectra, but they are all uniformly awful.

in this image (click to embiggen) I have posted the best spectrum from figure 3.11 (labelled "graphene with polyethylene glycol") above the spectra for polyethylene glycol (the PEG used in vaccines is PEG2000) and Graphene and graphene oxide (GO). The scales for the Raman shift are different in all the images, I can't do much about that. But the main thing is too look at the patterns.

The reports figure is very poor quality, so being sure of the peak locations is difficult but there are peaks around 800, 1100 and 1400 Raman shifts (cm-1) the may correspond to the 830, 1108 and 1470 peaks for PEG. There are a bunch of other peaks that don't quite fit with PEG (eg the peak around 1700 cm-1).

Graphene and Graphene oxide (GO) have distinct peaks at 1354 and 1591 (cm-1). There is a peak in the mess that is around 1600 cm-1 but the 1354 peak is missing.

So, no graphene.

The other images are worse. The Graphene nanoform from figure 3.11 (click to embiggen), clearly has no Graphene spectral characteristics. Likewise the graphene nano-objects in figure 3.18 have no spectral signatures of Graphene. 


Summary:

The "evidence" for graphene in the vaccines is random fibers and blobs which are not nano-scale, and poor resolution Rama spectra which don't show the spectral signature of graphene.

So no graphene in vaccines.

Given the poor image resolution the amateurish backgrounds and the obvious artefacts, the heading of "Global Humanitarian Crisis Prevention and Response Unit" on every page with a terrible graphic logo, I can't help but wonder if this is some sort of joke.

EDIT: 

The vaccines of course have a lot more things in them than just polyethylene glycol and mRNA, eg. the Moderna vaccine has cholesterol, 2000 dimyristoyl glycerol and 1,2-distearoyl-sn-glycero-3phosphocholine amongst others, Cholesterol has prominent peaks at 1131, 1438 and 1669 cm-1 which could explain what is seen in the spectrum in figure 3.11. In fact, may organic molecules will have similar peaks. There is no indication the spectra were searched against public or commercial spectra databases to generate identification.

Anybody serious about identify spectra would have at least run a control with a mix of authentic PEG and authentic Graphene. this was not done.


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Thursday, November 18, 2021

 

No, you can't "Detox" from the COVID vaccines (or any other vaccine)

You may have heard of people offering "Detoxes" to"remove" the COVID vaccines. These range from "Detox" baths of Epsom salts and/or Borax, to snake venom removal kits, to the ancient technique of cupping.

None work, some are dangerous and all are based on a complete misunderstanding of how vaccines work.

The currently available vaccines are mRNA vaccines (Pfizer, Moderna), and adenovirus vector vaccines (AstraZeneca, Jannsen). In the first two, the mRNA from the spike protein is encapsulated in a lipid shell, in the latter two this is carried in a viral particle.
When the injection is given into the muscle tissue of your arm the vaccine solution containing the vectors (be they lipid nanoparticles or virtual particles) rapidly distributes into the extracellular water (the fluids between the cells in tissues) and the particles bind to cells and deliver the mRNA into the cells.By the time a "detox" method is applied, most of the vector particles will have already delivered their mRNA payloads into the cells.Borax, Epsom salts, and the like "detoxes"  act by being a hypertonic solution (ie being much "saltier" than your tissue fluid), drawing body water out as your body tries to dilute the concentrated salt solution it is immersed in.
But this is the issue, these salt baths will remove water, but not large molecules like the lipid or viral particles (any that have not already been taken up), these cannot pass the tissue barriers In your body (if anything, it will concentrate the vaccine components slightly in your tissues). While Epsom salts are largely benign on the skin, Borax can cause skin and eye irritation, and some people have reported skin burns from its use. It definitely should not be consumed.Snake venom extraction kits have been also proposed to "suck out the vaccine", they apply negative pressure to draw fluid out,  as for the detox baths they will not draw out any vaccine, just a little (if any) tissue water and possibly concentrate the vaccine. They don't work for snakebite either and may cause tissue damage.https://www.snakebitefoundation.org/blog/2019/1/20/the-truth-about-commercial-snakebite-kits-and-venom-extractorsCupping has also been proposed to remove vaccines. In cupping heated cups are placed on the skin to create a partial vacuum next to the body as the air inside the cups cools down. This might draw out a little body water but will not remove the vaccine. If anything it might increase vaccine absorption. https://www.newscientist.com/article/2296526-covid-19-vaccine-tested-with-suction-technique-similar-to-cupping/
Cupping tends to leave large bruises from bursting blood vessels, a version called wet cupping involves cutting the skin to draw blood before applying suction with the cups. This will draw some blood from the broken surface capillaries but not draw out the extracellular fluid from deep in the muscle where the vaccine was injected.

So bottom line: Vaccine "detoxes" at the best will increase the uptake of the vaccine and at the worst cause harm, without removing any vaccine.

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Wednesday, February 13, 2013

 

New Posts on Asteroid 2012 DA14

The ABC has an article of mine on how to see the the close approach of asteroid 2012 DA14 using binoculars (and some handy ways to visualise the scale of the encounter).

And I've just published an article in  The Conversation about the loss of asteroid hunter Rob McNaught's funding and what it means for detecting potentially hazardous objects using 2012 DA14 as an example. 


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Friday, December 07, 2012

 

December 11, Alternative Medicine versus Science: Winners and Losers (ASCSA Public Event)

The Australian Science Communicators (South Australia) is holding a public event on Tuesday December 11 from 6 pm, Alternative Medicine versus Science: Winners and Losers

The presentations will examine Pseudoscience, particularly in the context of Medicine. Our distinguished panel comprises real scientists and science communicators, all with a healthy disrespect for those who would tout snake oil. It promises to be a cracking good night.

I'm one of the presenters, and I'll be giving you a small dose of homoeopathy. The others are:
Professor Rob Morrison (Science Communicator): What and why about Friends of Science in medicine; why pseudosciences are not science
Tory Shepherd (Journalist, The Advertiser): Pseudoscience and the public, the media angle
Professor  Marcello Costa (Prof of Neurophysiology, School of Medicine, Flinders University): Moving science into the medical arena
Professor Alastair MacLennan (Professor of Obstetrics and Gynaecology, Faculty of Health Sciences, University of Adelaide): In depth case studies for medical impact on women/children’s health

Location:
The Science Exchange 
55 Exchange Pl Adelaide, SA 5000 Australia
Tuesday, December 11, 2012 from 6:00 PM to 7:30 PM (CST)

Book via  EventBrite here: http://ascsapseudoscience.eventbrite.com.au

Cost:
ASC members & RiAus members: Free
Non-members: $5

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Thursday, August 09, 2012

 

A Plea for Sky Literacy


Venus, Jupiter and Aldebaran in the early morning sky around 6:20 as seen from Adelaide. click to embiggen

Over the past few years there has been a lot of effort to improve science literacy, the ability to understand the scientific process, given the importance of science to many parts of our lives..

I'd like to make a plea for sky literacy. The catalyst for this is a recent YouTube video purportedly of the fantasy planet Nibiru. The author laboriously points out various items as Nibiru, it's sun and a brown dwarf. Except he's looking at Venus, Jupiter and Aldebaran.

Now, Venus has been mistaken for other objects before, just this year it was mistaken for a flare and an oncoming aircraft. But it beggars belief that someone with an interest in finding unknown objects in space, in an era where there are lots of SmartPhoneapps that will help you find your way about the sky, could mistake our two brightest planets and the Brightest star in an iconic constellation (Taurus the Bull) for wayward super-Jupiters.

Okay, he could have been pulling our legs, but sufficient numbers of other people were also fooled. In weeks past a variety of ordinary astronomical phenomena have been identified as the illusory Nibiru (or some other planet X), only recently the Pleiades were identified as a mystery planet and moons.

How did it come to this, where people can no longer identify iconic parts of the sky? Light pollution plays a part, but in all but the most light polluted city centres the brightest stars and planets are readily visible.

Most of us now live largely divorced from our skies. We lurk inside our houses or flats, drive to and from work in enclosed vehicles, and if we do see the sky it's a thin slice divorced from context by looming brick and concrete structures, illuminated within an inch of their lives.

Southern Cross in the early evening southern sky.

We have lost connection with our environment, and with that our heritage in the sky. Many people have told me that they could not find the Southern Cross, emblemic of Australia and a key celestial navigation aide, if their lives depended on it. 

But knowing where the bright planets and stars will be in the sky is not just a matter of scientific knowledge, and their roles in our mythology and history, these things are beautiful in their own right. We have been slowly cut off from a source of joy in our world that is simple and completely free.

What do we need to improve sky literacy? I'm going to make an unusual suggestion, we should encourage people to walk more in the evenings. 

If you are out walking the streets of your suburbs and towns you are more likely to look up and see the beauty of the sky, the crescent Moon near a bright planet, the flash of  an iridium flare, the quick burn of a meteor. You don't really need to know the names of these things, if you are out often enough to follow the slow change of the sky over the seasons you will get a feel for what the sky looks like (if you look up).

If people see these things they will be more likely to inquire about them, and learn at their own pace. As a bonus it will improve our health to be out walking.

Of course, there's a lot that needs to be done to encourage walking, there actually has to be decent footpaths for people to walk on, the streets need to be safe to walk in the evening, the lighting has to be bright enough for people to walk comfortably, but not so bright that it drowns out the sky. maybe even the occasional sky watching sign, like the constellation maps our local city council has erected.

But interms of improved health, better social connectedness as walkers meet each other and reconnection with our sky, it is well worth the effort.

And we will be less likely to be subjected to videos of someone mistaking  a bright planet for a passing super-Jupiter.

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Wednesday, December 14, 2011

 

I'm on Today Tonight, umm Thursday Night Tonight

ChemSpider 2D Image | bisphenol a | C15H16O2 UPDATE: It's Thursday Night 6:30 pm I've been advised it's either tonight (Wednesday) 0r tomorrow night

UPDATE to UPDATE: The video should be on the website http://au.news.yahoo.com/today-tonight/ the day after, and will be up for about a week.

those of you who are in South Australia, I will be on a Today Tonight segment (Channel 7) tonight (Wednesday December 14), briefly looking silly while peering at tins.

This will be eventually repeated on the East coast. And I'll be on again in one to two weeks time in a different story.

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Friday, December 09, 2011

 

In Which I am a Media Star Again

Explanations later in the week.

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Friday, July 22, 2011

 

Now THAT'S the Way to Test a Theory (Yes, Elenin Really is Small)

There has been a lot of angst about the size of comet C/2010 X1 Elenin on the internet, with some people worried it is either a Brown Dwarf Star or the Satellite of a Brown Dwarf. Both Leonid Elenin and I have used maths and simulations to show that the comet must be small, but people continue to be anxious, and are discussing the matter endlessly on various discussion groups.

Except a commenter called Astronut, who did something unthinkable, rather than endlessly nattering he actually tested the hypothesis that Elenin was big.

He bought time on a remote telescope (one of the Slooh scopes) in the Canary Islands, and measured the position of asteroid (74732) 1999 RQ176 twenty -four hours after it's close encounter with comet Elenein on May 20.

And it was exactly where it was predicted to be (see also Leonid Elenins images of the asteroid post encounter).

Now, this pass was very close, at it's closest 1999 RQ176 was 225,830 km from Elenin (around 0.002 AU), which is 0.59 of the average distance between the Earth and Moon. If Elenin was as massive as Jupiter, it would have substantially altered the asteroids location. And I mean substantially, not just a few arc minutes off, more like being degrees off, the asteroid sling-shotted off into deep space.

Actually, if Elenin was a Brown Dwarf, with a radius of 4 times that of Jupiter (285 968 Km), at closest approach the asteroid would have been deep inside the Brown Dwarfs photosphere, and wouldn't have come out again.

The very fact that we could see 1999 RQ176 at all, means that Elenin is not a Brown Dwarf.

Science is at its heart a practical enterprise, we test things, and Astronut has shown that citizen scientists can make significant contributions, all props to you Astronut.

UPDATE: Astronut follows up the observations here.

PS, if Astronut or one of Astronut's friends reads this, could he/she get in contact with me, Global Rent-a-Scope has an offer for you.

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Tuesday, July 19, 2011

 

If You are Looking For "Comet Elenin a FAQ for the worried"...

.. it's been taken down by blogger, along with two other Elenin related posts (see below) for alleged violation of the Digital Millennium Copyright Act (DMCA) . Given that there is no copyrighted material on these sites (either material generated entirely by me or links to and citation of publicly available material), this is just a frivolous attack on people countering Elenin nonsense. I expect this will be reversed soon. But in the meantime

http://astroblogger.blogspot.com/2011/05/comet-2010-x1-elenin-earthquakes.html
http://astroblogger.blogspot.com/2011/03/from-super-moons-to-comet-elenin-we.html
http://astroblogger.blogspot.com/2011/04/comet-elenin-faq-for-worried.html

are not available.

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Sunday, December 19, 2010

 

Citizen Science - You Too Can Hunt for Exoplanets

Aph10144093
From the folk who bought you the citizen-participation astronomy projects Galaxy Zoo, Moon Zoo and the Milky Way project comes Planet Hunters. You can help find extrasolar planets for the Kepler Space telescope team.

At planet hunters you scan star-intensity traces from the Kepler Space Telescope looking for the characteristic dips in a stars intensity caused by a planet transiting in front of of the star.

The Kepler folks have computer programs to do this, but people tend to be better at finding the patterns of transits than computers. So this is you chance to aid sicence, and mybe find another world out there. I'm enrolled, but so far I've only found variable stars (see image above). You will need a fair bit of patience as your sort through the traces.

But still, finding another world! Imagine that!

(Tip of the hat to the Bad Astronomer)

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Sunday, November 14, 2010

 

Geo-xcentricities part 2; the view from Mars.

Einstein rings, a spectacular prediction of relativity, taken from Hubble (Image credit Hubble/NASA)

You may remember a little while back I wrote about a conference of modern Geocentrism (Galileo was Wrong). Geocentrism is the belief that Earth is the centre of the Solar system, nay the entire Universe and everything revolves around it.

Todd Wood attended the conference, and you can read the about his growing sense of incredulity in his posts (part 1, part 2, part 3, part 4, part 5).

It turns out that these folks are relativity deniers.

Image of the crescent Earth and Moon on October 3, 2007, taken by the HiRISE instrument of the NASA’s Mars Reconnaissance Orbiter.

Which is pretty strange, the usual tack is to argue for Geocentrism based of relativistic frame equivalence. Arguing against relativity is pretty hard, as it is one of the best confirmed theories of physics we have. From gravitational lensing (see images above) to frame dragging, relativity has passed increasingly stringent tests with flying colours.

These geocentricists apparently need relativity disconfirmed so the the Michelson-Morely experiment proves the Earth at rest.

Now there is a lot of problems with this (not the least because they need a non-moving ether to explain the M-M experiment, then a moving ether to explain Foucault's Pendulum) and other geocentrist positions. Some of the problems can be demonstrated with intensive mathematics, some with not so much maths (like the claim that GPS doesn't use relativistic corrections, which is untrue.)

Earth as seen from Mars taken by the Spirit rovers' panoramic camera in 2004.

However, in the spirit of my first post on this conference, where I tried to get people to do observations themselves that disproved first the Ptolemaic then the Tychonian systems, I want to get people to do something much simpler, related to observational astronomy.

Also in the spirit of Einstein, who tried to imagine what the word would look like if you were travelling on a photon, I want you to imagine your are standing on Mars.


The evening sky on Mars on April 29, 2005 as simulated by Stellarium (the location isn't at the same latitude and longitude as opportunity, so the view is slightly different from the rover).

What would you see from the surface of Mars that would be different in a Tychonian system (the system favoured by our modern geocentricists) versus a heliocentric system system?

As the Tychonican system is an inverted Copernican system, things like the phases of the Earth would be identical (see this JAVAscript model, advance the time to October 3, 2007 to match the image of crescent Earth and Moon above, and flip between the Tychonian and Heliocentric models to see what I mean).

Earth imaged by the panoramic camera of Opportunity an hour after Sunset on April 29, 2005 (Image Credit NASA/JPL).

There is a big difference that would be immediately apparent. Whether in the Tychonian or Heliocentric systems, from the point of view from Mars, Earth would appear to be a morning or evening star that appeared to revolve around the Sun.

However, the geocentricists are using a geostationary model, where the 24 hour day is produced by the Sun rotating about the Earth. So in a period of 24 hours, an observer on Mars (armed with an occultation disk) would see Earth rise from the sun, then fall back, then reappear on the other side of the sun and repeat the process again.

During the period that the Mars rovers took images of the Earth, at maximum elongation Earth was 42-47 degrees from the Sun as seen from Mars. For the Earth to move from maximum elongation to inferior or superior conjunction (at least, as it would appear from Mars, because in the Tychonian system Earth can't have conjunctions) takes 6 hours (in a 24 hour day there will be four 6 hour segments as the Earth goes out, comes back, goes out and comes back again from the solar disk).

So the Earth will appear to move 42 degrees (taking the lowest figure) in 6 hours, or 7 degrees per hour against the background stars (approximately, it's slightly more complicated than this, but rough figures are all we need). That's 14 Lunar diameters per hour! Earth is fairly hooting along compared to the background stars. In one minute Earth would move 1/4 of a Lunar diameter which is quite noticeable.

Now look at the image above. It is a composite of 3 x 15 second images taken with the panoramic camera, you can see the image of Earth is slightly elongated. However, remember that Mars rotates, and any 15 second exposure will cause slight star trailing due to its rotation. The trail we see of Earth is nothing like what we would expect if it was moving to a 24 hour rhythm, as it hares along the sky (roughly 1/5th of a Lunar diameter). Still, for confirmation we have to check Earth's movement against that of the background stars.

Fortunately, in the original image there is a background star just above Earth (it's best seen in the TIF file). It has the same degree of elongation that the Earth does. This falsifies the Tychonian system, thus the solar system is heliocentric.

So "Eppur si muove" because it um, doesn't move (with respect to the background stars as seen from Mars).

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Thursday, September 23, 2010

 

Me, Mercury and the European Planetary Science Congress

mercury with tailThis is an image of Mercury's tail obtained from combining a full day of data from a camera aboard the STEREO-A spacecraft. The reflected sunlight off the planet's surface results in a type of over-exposure that causes Mercury to appear much larger than its actual size. The tail-like structure extending anti-sunward from the planet is visible over several days and spans an angular size exceeding that of a full Moon in the night sky.(Credit: Image courtesy of Boston University’s Center for Space Physics)

Back in 2008 Comet Al and I were trying to confirm a comet position in images from STEREO A. I pointed out the nice bright comet moving across the STEREO image field and Comet Al said, "That's not a comet, that's Mercury!". We exchanged the internet equivalent of startled looks.

The feeling on the Stereohunter list was that it was an artefact, but I remembered an article on sodium emission from Mercury, and went to track down the group and ask them what they though our tail might be.

So began a saga that cumulated in the paper "Observations of Mercury’s Escaping Sodium Atmosphere by the STEREO Spacecraft" by Carl Schmidt, Jeffrey Baumgardner, Michael Mendillo, Christopher Davis and Ian Musgrave being read at the European Planetary Science Congress today. This paper was the subject of a press release, and has spread wide into the internet (Science Daily, Space.com, and SpaceInfo are just a few examples).

I must say I'm mildly chuffed to be mentioned in press releases, I'm more chuffed that I was included in the paper. I've got 40 peer-reviewed papers of my own in the field of biomedical science (ask me about Maitotoxin!), some of which I am very proud of, so I'm no stranger to being published.

But this is the first time my amateur efforts have made a contribution to advancing astronomical research, my beloved hobby. Of course, the others did all the really hard work of ground observations and calibrating the Stereo images, so my contribution needs to be put into perspective, but still.... ther's that warm inner glow that in a small way I made a difference.

My blog posts on the tails (with nice images and animations and a bit more background), can be found here.

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Thursday, September 16, 2010

 

Geo-xcentricities; you too can be Galileo with just a pair of binoculars (and gaffer tape)

geocentrism_flyerThere’s been a lot of blank disbelief on the blogosphere of late, due to the announcement of a conference on Geocentrism (Galileo was Wrong). Geocentrism is the belief that Earth is the centre of the Universe and everything revolves around it. You would think that, 400+ years after Galileo, people would have cottoned on the the idea that the Earth orbits the sun, the sun orbits the galactic centre and the Milky Way galaxy does … well …complicated stuff with other galaxies, but basically we worked out long ago that the Earth is not the centre of the solar system, let alone the Universe.

Other people, especially Ethan at Starts with a Bang and the Bad Astronomer, have dealt with the technical details (and I have an earlier discussion here and here). My goal is to get you, the ordinary person on the Clapham omnibus (or in my case, the Outer Harbour train, where I am writing this), to try and demonstrate the Earth is heliocentric for yourself and to do so with common household materials. After all, science is at heart a practical endeavour, and non-professionals should be able to find the evidence for themselves.

So for this journey into the starry spheres, we will need a pair of binoculars, a camera tripod, some cardboard and alfoil, and lots of gaffer tape. We also have some luck, as the sky is currently cooperating in the Geocentrism debunking stakes.

First we have to ask ourselves, which “geocentric” theory are we disproving. The classic geocentric theory is that of Ptolemy, in which the planets, Moon and the Sun all orbit the Earth. The most famous variant of this is Tycho Brahe’s helio-geocentric system, where the Sun and Moon orbits the earth and everything else orbits the Sun. There are important differences in the systems which we will explore later.

First off, let’s look at the phases of Venus. For this you will need binoculars and the camera tripod. You will also need a way of attaching the binoculars to the tripod. These days I use a special attachment (but this requires modern binoculars that have a screw thread on the body), but in the past I have used gaffer tape to good effect. Why attach the binoculars to the tripod? Because otherwise there will be too much shaking for you to see the image properly.

The image to the left is the setup I use for observing Sunspots (we come to that later), showing the binoculars gaffer taped to the tripod.

At the moment, Venus is prominent above the western horizon. Point your binocular lash-up at Venus, in my 10x50 binoculars Venus is very small but is a disk which has a distinct “half –Moon” shape. If your binoculars don’t have decent anti-glare coatings, you may have to observe in the early twilight in order to see Venus’s shape without internal reflections from the binocular lenses getting in the way.

As you watch over the coming weeks, you will see Venus expand in size and become more crescent- shaped. Sketch the shape so you can follow its progress. This is so fast you should see a visible change in just one week. By mid-October Venus will be a thin crescent almost 2/3rds bigger than when you started observing. By late October Venus has nearly doubled in size and is a thin, glistening wire. Then Venus vanishes into the Suns glare and reappears in the morning. Over the next few months you can watch Venus shrink and become a tiny disk.

And now you have demolished the Ptolemaic geocentric system. Venus does have phases in this system, but quite unlike what you see here (I leave it too the reader to work out what a Ptolemaic systems Venus phases would look like, you can see a model of Ptolemaic Mercury here, which will give you a good idea). And you have only taken almost 6 months to do it (what, you thought it would be easy). As a reward, here's an animation of the Phases of Venus.




Left image Jupiter above the eastern horizon, Right Image, Venus above the western horizon, both at the same time in the evening (around 8pm ish in mid September 2010).

But wait! You say What if it is just an illusion, a trick of the optics? Well, you have a control. Having observed Venus, swing your binocular lash-up to the east, to the brightest object there (and second brightest non-lunar object in the night sky after Venus), Jupiter. Jupiter is a distinct oval in my binoculars, and the four bright Medicean Stars glitter around it. Over the nights you watch Venus swell and thin, keep an eye on Jupiter as it does…well…nothing.

Jupiter and three of its moons imaged with a mobile phone.

But Ah! The Medicean Stars, now known as the Galilean Moons, they will shuttle backwards and forwards during the nights as you watch. The realisation that these “stars” were Moons of Jupiter were not a blow to any form of geocentrism per se, although they were the second of a series of powerful blows against the Aristotelian physics that underpinned Ptolemy’s system, which aided its demise. Determining that these specks actually orbited Jupiter, and were not just accidentally there, took a lot of effort.

Try keeping track of these sparks, and without reference to an almanac, try and determine their orbits (heck, try and keep track of which near identical points of light are which). It may take a while, you will need to keep careful sketches, and track the Moons and Jupiter with respect to the stars as Jupiter moves through the heavens, but a) You are sketching Venus anyway and b) it will be well worth it (hey, you proving things for yourself!).

The next bit is more demanding. The Phases of Venus demolished the Ptolemaic Geocentric system, but the Tychonian- Geo-heliocentric system had Venus phases just like a pure heliocentric system (which is not surprising, as Tycho’s system is an inverted Copernican system). To eliminate the Tychonian system, we need to observe sunspots.

Luckily the Sun is coming out of its quiet phase, so you will have some to record. For this you will need to set up a safe binocular projection system (as shown above), where the image of the Sun is projected onto a surface so you can record the Sunspots. NEVER LOOK DIRECTLY AT THE SUN WITH BINOCULARS AS SEVERE EYE DAMAGE WILL RESULT.

Anyway, while you are recording the Phases of Venus and the orbits of Jupiters’ Moons, record the passage of Sunspots over the Suns face, over the 5-6 months you are recording the susposts, you will notice the path taken by the sunspots moves up and down. This is due to the Earths orbit not being exactly in the plane of the Suns rotation. In a geocentric system, with the Sun orbiting the earth once a day, this variation would show up on a daily basis, but what you observe can only be seen in a heliocentric system.

So, congratulations, you have just demonstrated that geocentric models don’t describe the solar system we see using very simple tools. It took a while, and was hard work, but you have demonstrated it yourself, and all the blovation of geocentricists won’t take that away (yes, Stellar parallax gets all the glory, but annual Sunspot variation was a powerful blow to Tychonian geocentric models). If you want to, you can take this further by making your own Foucault's Pendulum.

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Thursday, September 02, 2010

 

See Baroness Greenfield at the Florey Lecture (Friday September 3)

The Florey Lecture is an Annual Public Lecture at the University of Adelaide where a distinguished international scientist talks about some aspect of medical science and how it touches our lives.

This year the Scientist is Baroness Susan Greenfield, a renowned scientist and top notch communicator, I can promise that her talk will be fascinating. This year it's on how technology may be rewiring our brains.

The lecture is 5:30-7:30 pm Bonython Hall,University of AdelaideNorth Terrace, Adelaide
South Australia (L11 on this printable Map). Entrance is by gold coin donation, and you can register for entry here.

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Saturday, August 14, 2010

 

Ask The Naked Scientist! - National Science Week 16 August

As part of National Science Week, Ask The Naked Scientist is happening on Monday, August 16 at 7.00pm in the Napier Theatre, University of Adelaide, North Terrace, Adelaide (K12 on this printable Map). Entry is free and no bookings are required.

This is an audience-interactive science question and answer show. Taking questions from the public on any science-related topic, Dr Chris Smith of Cambridge University responds in innovative, informative – and sometimes hilarious – ways.

A medical doctor and clinical lecturer in virology at Cambridge University, Chris Smith founded The Naked Scientists, an award-winning radio program on the BBC (and one of the world’s most down-loaded podcasts) that aims to strip science down to its bare essentials. Chris is one of the international guests touring the country in National Science Week.

Held in conjunction with Australian Science Communicators SA.

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Monday, August 09, 2010

 

A Paper on Fructose and Cancer, it doesn't mean what you think it means

Over at Respectful Insolence Orac has discussed the misrepresentation of a study about the effect of fructose on pancreatic cancer. This post is a slightly expanded version of that comment, with some added diagrams and a bit more on fructose concentrations. The point is still that the press release (that limiting fructose intake may disrupt cancer growth), and some of the conclusions of the paper, are not justifyable from the data.

First, a little background. Sugar to most people is sucrose, or cane sugar. But actually "sugar" covers a large number of similar chemical compounds. Ones commonly encountered apart from sucrose include glucose and fructose (also known as fruit sugar as it is found in high concentrations in fruit, it is also found in honey). Indeed sucrose is glucose and fructose linked by a chemical bond. When you eat sucrose, enzymes in your gastrointestinal tract break it down into glucose and fructose, which are then absorbed (your body can absorb intact sucrose).

There is some concern that consumption of high levels of fructose may have negative health consequences above that of simply consuming more calories. People in the United States are particularly concerned as many of their soft drinks and foods are sweetened with High Fructose Corn Syrup (HFCS), as opposed to sucrose in most of the rest of the world (like Australia, where sugar cane fields are part of the national psyche). It should be pointed out that the proportion of fructose in honey is about the same as that in HFCS and some fruits (eg apples and pears) have significantly more. However, the large amount of extra sugar added to processed foods and soft drinks means we are be exposed to much higher concentrations of fructose (and glucose) than we would eating a diet of fresh fruit and vegetables.

In the study Orac talks about (Cancer Res; 70(15) August 1, 2010) the researchers were looking at whether fructose could support cancer cell growth.

Now in the paper there are two sets of results, one set on cancer cell proliferation, and one set on metabolism (seeing whether metabolic pathways involved in cancer growth were selectively activated by fructose). The authors show reasonably convincingly that fructose is preferentially metabolised to nucleic acids in pancreatic cancer cells, pancreatic cell models and hepatic cancer cells (with some caveats I will cover later[1]). However, what they say about the rate of cancer proliferation is almost, but not completely, dead wrong.

Press release:
"These findings show that cancer cells can readily metabolize fructose to increase proliferation," Dr. Anthony Heaney of UCLA's Jonsson Cancer Center and colleagues wrote.
Abstract:
These findings show that cancer cells
can readily metabolize fructose to increase proliferation.
If you have access to the paper, look at Figure 1. If not, I've abstracted some of the key results in Figure 1 below, and added a line showing the control level of proliferation for clarity.


Figure 1, panels A, B, C, D and F from
Cancer Res; 70(15) August 1, 2010








The first important thing to note is that when they did the proliferation assays, they compared the results to cells cultured in 10% Foetal Bovine Serum alone - which contained *0.4 mmol/L glucose*[2] (FBS in the figure, open bar, the black bar is complete medium with 10% FCS and 18mmol/L gulcose) . This means at the lowest concentrations of additional sugar, they are comparing 400µM glucose + 5.5µM fructose vs 405.5µM glucose. Which kind of messes up their interpretation.

Looking at the graph (note the red line showing basal growth, and the error bars) Generally, glucose and fructose are the same...they don't do anything above and beyond the Foetal Bovine Serum control. Only in MiaPaCa-2's, HPAF and, possibly, HPDR6 do you see proliferation which MAY be statistically significant from the baseline proliferation at the highest concentrations used (400µM glucose + 5500µM fructose vs 5900µM glucose, they look higher, but the error bars are significantly bigger too). An important caveat is that for the MiaPaCa-2 cells, when proliferation was remeasured using a different assay (BrDU incorporation), fructose basically did nothing. So any apparent increase in proliferation may just be assay variation.

It's a bit hard to clearly work out what data points are statistically significant, if any, as their statistics are borked, badly borked. The legend to Figure 1 says "P = not significant, fructose versus glucose or normal medium (NM)." Which if correct, means that the proliferation rates at 5.5µM added sugar (glucose of fructose) is no different from the 18 mM glucose normal medium values, which makes their data uninterpretable (see Figure 1B and C particularly). No other stats tests on the proliferation data are presented anywhere.

So we should reformulate the statement of the abstract as "In some cancer cell line, 5 mM fructose and 5mM glucose might cause the same amount of proliferation above that found with 0.4 mmol/L glucose, if we could statistically distinguish them from the control" (actually, the best interpretation is that fructose and glucose did nothing to proliferation, if their presentation of the statistics is correct).

Now, the kicker, what is the plasma concentration of fructose in most people? It's 8 µM, even in diabetics it's only 12 µM, while plasma glucose in normal people is around 5000µM (doi: 10.2337/diacare.25.2.353 Diabetes Care February 2002 vol. 25 no. 2 353-357, other papers have found diabetics in ketoacidosis to have levels of around 88µM, which dropped to 11µM when their diabetes was controlled [Clin Biochem. 2010 Jan;43(1-2):198-207. Epub 2009 Sep 8.]).

This is probably due to fructose being mainly taken up and metabolised in the liver, but the bottom line is that pancreatic tissue will never see any more than micromolar concentrations of fructose. Even if plasma levels of fructose from dietary sources reached 55 µM (which would be insanely unlikely), it would, on the basis of the results presented in the article (Cancer Res; 70(15) August 1, 2010) do absolutely nothing to cell proliferation (see Fig 1 again). The authors report that pancreatic cancer patients have 2.5 times the plasma levels of fructose of non-cancer patients, but that is still is 100 times less than the 5mM needed to see any difference in proliferation rate (assuming that the results are statistically significant, which they may not be).

There is one tissue that could be exposed to high levels of fructose, and that is the liver, which receives blood flow direct from the gut. However, even high levels of fructose ingestion (4g/kg; about 10 times what you would get from a can of soft drink) produce concentrations of fructose of no more than 1-2 mM in the portal blood (J Am Coll Nutr. 1986;5(5):443-50., Nutr Metab 1971;13:331-338 (DOI: 10.1159/000175352)), still well below the levels where we see some increase in proliferation of pancreatic cancer cells (well, assuming the results were statistically significant, which they may not be; the hepatic cancer cells were not examined for proliferation effects). Even then, the cells exposure at these high levels is brief, at most 2 hours, whereas in the experiments the cells were exposed for 48 hours. So even if you do drink 10 cans of soft drink at one sitting, your liver cells will be unlikely to be exposed to the proliferative levels of fructose.

Put simply, their results do not support their conclusions on prliferation.

1. While the data on metabolism is clear, again these results are in cells exposed to unphysiological concentrations of fructose for 72 hours. This is completely different from what the cells in your body would be exposed to.

2. It is very hard to get rid of glucose from FCS, and if you did the cells wouldn't grow (and actually die at 0 glucose). And you can't get rid of the FCS, for it contains growth factors the cells need to grow as well. Well, there are serum-free media with added growth factors, but they have their own problems. So there are limitations in how they can study this question. Most of my work is done in cancer cell lines (PC-12 and SHY-5Y amongst others, so I am acutely aware of both the strengths and limitations of tissue culture.

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Thursday, August 05, 2010

 

National Science Week 14-22 August

National Science Week (14-22 August) actually starts this weekend in SA with Science Alive at the Wayville Pavillion, it promises to be even nbetter this year than last year, and least year was pretty good. As well as local state events theres The Big Sleep Survey citizen science research project and a National Tour of scientists.You can find your local state activities here.

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Thursday, July 01, 2010

 

Anti-Science Bullies at it Again

You may remember how the British Chiropractic Association sued Simon Singh because he had the audacity to sepak the truth about Chiropractic. Now a medical testing firm, Doctors data, is suing Dr. Steve Barrett of Quackwatch, for criticising it. Well warranted and scientifically supported criticism. You can read more detail at Respectful Insolence. As with the Simon Singh case, pass the news on so we can raise awarness of this latest round of anti-science bullying, and you can contribute to Dr. Barrett's legal defense fund by donating to Quackwatch here.

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Friday, April 16, 2010

 

Woo Hoo!! Simon Singh Wins!

Simon Singh, scientist and science writer, who was being sued by the British Chiropractic Association for the temerity of writing the truth, has had the libel case against him dropped. While this is a win and cause for celebration, there's a long way still to go. As Simon writes:

“It still staggers me that the British Chiropractic Association and half the chiropractors in the UK were making unsubstantiated claims. It still baffles me that the BCA then dared to sue me for libel and put me through two years of hell before I was vindicated. And it still makes me angry that our libel laws not only tolerate but also encourage such ludicrous libel suits. English libel law is so intimidating, so expensive, so hostile to serious journalists that it has a chilling effect on all areas of debate, silencing scientists, journalists, bloggers, human rights activists and everyone else who dares to tackle serious matters of public interest. In the area of medicine alone, fear of libel means that good research is not always published because those with vested interests might sue, and bad research that should be withdrawn is not pulled because the authors might sue the journal, and in both cases it is the public that loses out because the truth is never exposed. My victory does not mean that our libel laws are okay, because I won despite the libel laws - we still have the most notoriously anti-free speech libel laws in the free world.”


Read more here, and see the commentaries by Bad Science, Respectful Insolence and Pharyngula.

If you want to help in the campaign against the flagrant misuse of libel laws to silence critics go to Keep Libel Laws Out of Science.

free debate

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