Physical Insights

An independent scientist’s observations on society, technology, energy, science and the environment. “Modern science has been a voyage into the unknown, with a lesson in humility waiting at every stop. Many passengers would rather have stayed home.” - Carl Sagan

Archive for the 'health physics' Category


Quote of the week.

Posted by Luke Weston on July 23, 2008

A beautiful analogy to explain why the LNT hypothesis seems like it might be something of a stretch:

DV82XL Says:
July 22nd, 2008 at 12:04 am

If the LNT were applied to falling as it is to radiation, we might note that 100 percent of those falling onto concrete from 100 feet are killed, but only 50 percent of those falling from 50 feet die. With these data we would linearly extrapolate to say that 10 percent falling from 10 feet and one percent of those falling from one foot would die. Armed with this “linear no-threshold falling theory,” we could confidently assert that jumping rope should be banned on all school playgrounds since statistically anyone making 100 one-foot jumps would die.

Posted in health physics, linear no-threshold | Tagged: , | 3 Comments »

Not your average anti-nuclear-power group.

Posted by Luke Weston on May 21, 2008

This is worth checking out.

EFMR Monitoring Group

I will quote a few sentences from the website, to show what this group is generally about.

The EFMR Monitoring Network is a non-profit, non-partisan organization which monitors Three Mile Island Unit 1 (TMI) and Peach Bottom Atomic Power Stations 2 & 3. The Group was formed out of a Settlement with GPU Nuclear in 1992 relating to Post-Defueling Monitored Storage at TMI-2. In January 1999, the new owners of TMI-1, AmerGen, (PECO Energy & British Energy) agreed to terms with EFMR through 2006. Additionally, EFMR expanded its monitoring and research activities to include Peach Bottom 2 & 3 as a result of Universal Settlement relating to the merger of PECO Energy with Commonwealth Edison.

This is not your average dogma-packed “no nukes, no nukes, no nukes” activist group. Nowhere in their mission statement does it call for or support the closure of existing, operating, safe fission power plants.

EFMR maintained five low-volume air samplers on the east and west shores of the Susquehanna River opposite of TMI from 1993-1999. Dickinson College Physics Department collected the filters and cartridges of these monitors on a weekly basis. Analyses performed included, but were not limited to, weekly gross beta and alpha measurements, monthly gamma isotopic analysis, weekly Iodine-131 analysis, and semi-annual Strontium-90 analysis. The last collection occurred in December, 1999.

In November, 2000, EFMR deployed a low-volume air sampling station at Peach Bottom.

This is a neat idea! Of course, every nuclear power plant meticulously monitors any discharge of the very small amounts of radionuclides into the atmosphere or other effluents, and these records are all meticulously filed with the NRC, and are a matter of public record.

However, if they want to provide an extra layer of data, and extra monitoring apparatus, by themselves, then so much the better.

Having such data collected by independent means, and analysed by local college physicists, has every potential to:

a) Eliminate any community distrust of nuclear utilities.

b) Dispel the myth that nuclear power plants emit any aetiologically significant amounts of radioactivity into the environment at all during their operation.

c) In the event of a severe incident such as the Three Mile Island accident, improbable as though it may be, provide independent data to confirm the true magnitude of any release of radioactivity, and dispel baseless and false speculations or claims of very large and aetiologically significant releases of radioactivity being “covered up”

e) Educating people about natural background radiation and radioactivity and its sources, including atmospheric nuclear weapons testing, cosmic radiation and fossil fuel combustion, as well as about basic radiation instrumentation and health physics.

The only potential for a problem that I can foresee with this is that controversy may be generated over very small radioactivity releases which can be detected above background by sensitive instruments, which are however not in excess of NRC and EPA regulatory limits, and are of no public health significant - just like the controversy surrounding tritium effluents at certain nuclear generating stations in the US in recent years.

PECO has also agreed not use Mixed Uranium Oxide (MOX) fuel at Peach Bottom 2 & 3, Limerick Nuclear Station Units 1 & 2, and Salem Nuclear Station 1 & 2.

Well, I must say, I don’t agree with that. What is their reasoning behind making such a demand of the utility? What’s so bad about the use of MOX? I can think of several good points to be made of the use of MOX as a fission reactor fuel.

AmerGen has ensured that its work force meets or exceeds NRC staffing requirements and has agreed to pay excess decommissioning costs for TMI-1. AmerGen also agreed not to conduct business with any company, organization or nation that the United States of America is boycotting for economic or military reasons.

Well, how can you argue with any of that? Of course, the owner pays decommissioning costs for TMI-1, just like they pay the costs of decommissioning any other unit. I don’t think this represents any shift away from the obvious, in terms of the utility’s policy - the only difference being that TMI-2 will of course cost a bit more to decommission completely than the average reactor. I see no reason to believe that the TMI-2 accident will in any way affect the decommissioning of TMI-1 at the end of its life.

Of course any nuclear utility should meet or exceed anything the NRC requires of it. (If the NRC’s requirements are thought to be inappropriate, or too strict, or too soft, or whatever, then you take that up with the NRC - but of course the utilities should be by the book.)

EFMR has on-line access to AmerGen’s Reuter-Stokes, gamma monitoring system. This sensitive system collects samples, analyzes them, and prints out data on an hourly basis from 16 separate collecting stations located within a four mile radius of Three Mile Island. EFMR continues to attend NRC meetings, and receive regular briefings and updates from AmerGen, Exelon, and PECO Energy.

To monitor radiation levels surrounding the Three Mile Island Nuclear Station and the Peach Botom Atomic Power Station so that any deviation from normal background radiation levels are immediately detected and reported. This allows for a prompt response from our citizens network to provide independent data, especially in the event of another accident or any radiological release in the area.

If abnormal levels are detected, EFMR may report the data to proper authorities including the PA Department of Environmental Protection, the US Nuclear Regulatory Commission and others.

The network is comprised of ordinary citizens whom each record five radiation measurements per day. Each person had been provided a geiger counter equipped with an electronic timer to measure radiation levels.

At the end of each minute, it displays the counts in a liquid crystal display window. That user then writes the count on a data sheet along with the time and weather conditions. The monthly data sheets are collected and reviewed by professional advisors.

We also utilize five stationary low-level air samplers located within a two mile radius around Three Mile Island. These monitors are able to distinguish and record Alpha and Beta radiation. The data is collected by the Dickinson College physics Department and analyzed quarterly. A control station low-level air sampler is located a Dickinson College for comparison.

EFMR has distributed 75 RadAlert radiation monitors at 50 stations in an eight county area around Three Mile Island, including numerous colleges, high schools and community-based organizations. Several additional monitors are deployed in northern Maryland close to the York County border. In addition, EFMR will deploy 30 rad alerts in close proximity to Peach Bottom as a result of its Agreement with PECO Energy.

This all sounds good to me. Of course, the data taken needs to be analysed by those who understand what they’re doing, and in the event of any unusual and potentially release of radioactivity, the NRC and authorities need to be notified so that they may determine the most safe, prudent and rational course of action - of course, the utility will almost certainly be the first to notify the NRC, in any accident scenario.

The anti-nuclear lobby, and many environmentalist groups, could do well to learn from this group.

Posted in EFMR monitoring network, health physics, nuclear energy, nuclear safety, three mile island | Tagged: , , , , | 4 Comments »

The battle for Chernobyl.

Posted by Luke Weston on May 8, 2008

Last month I got into a discussion with some people about the Chernobyl disaster, following the 22nd anniversary of the catastrophic Soviet reactor accident, and this documentary film was mentioned:

The Battle for Chernobyl.

To put it lightly, this film is an astonishing bunch of rhetorical baloney.

I’m not trying to downplay the public health consequences of the Chernobyl accident - but I’m downplaying the inaccurate or false claims made by certain groups, as distinct from the body of evidence of real, documented and substantiated (and very significant impacts).

Despite the known public health impacts, some people continue to make claims that are either just not true or are completely unsubstantiated - for example any claim that there are children, today, with an increased incidence of thyroid cancer, which just isn’t true - any children who were exposed to the short-lived iodine-131 source term in 1986 are adults today, 22 years later, and the iodine-131 decayed away quickly, within months.

Now, to look at the video:

From the gaping hole, a spray of fire, charged with radioactive particles in fusion, sprays a thousand meters into the sky.

Right from the outset, it’s completely obvious that for the next hour and a bit, science is tossed aside, and rhetoric is the first and only order of affairs.

The radioactive fallout is going to be 100 times greater than the combined power of the two atomic bombs dropped on Hiroshima and Nagasaki.

Some simplistic comments have often been made in which the radioactive release of the Chernobyl event is claimed to be 300 or 400 times that of the bomb dropped on Hiroshima. However, in sensible terms of radiological impacts, the two events can not be simply compared with a number suggesting that one was x times larger than the other.

Radioecology after Chernobyl - some good literature.

The total combined energy yield of both of the nuclear weapons used in Japan was about 35 kilotons of TNT equivalent - or about 41 gigawatt-hours. The Chernobyl Unit 4 reactor, with a thermal power output of about 3 gigawatts, produced that same amount of energy, and created about the same amount of fission-product activity, every 13.6 hours or thereabouts. Given that a nuclear power reactor contains fuel that has provided that kind of power output for perhaps as long as several years, of course there’s a larger inventory of radioactivity contained in the reactor fuel.

Iodine tablets swallowed to counteract the effects of radioactivity.

Iodine prophylaxis only prevents the body from uptaking iodine from the environment - which might be contaminated by radioactive iodine-131. It in no way “counteracts the effects of radioactivity”.

“The radiation level above the reactor is over 3500 R, almost nine times the lethal dose.”

3500 R over what length of time? The strength of an ionising “radiation field” in such a situation can only sensibly be expressed as roentgens (or sieverts or similar unit) per hour (or per unit of time).

0:36:40

If over six hundred pilots were “fatally contaminated with radiation”and killed, and this is known to be true, why have the Chernobyl Forum, the IAEA, the WHO, the UNDP, the UNSCEAR, Russian or Ukrainian governments never mentioned it? Can it be proven to be true, before the international community, by these people?

0:37:08

Why does none of this film show any artefacts on the film resulting from radiation damage?

0:38:20

The infamous “elephant’s foot” “magma” doesn’t look “white-hot” at this stage, although that’s how it’s described.

0:43:45

Again, the level of radioactivity is implied to be so very high - and it was high - yet it was not high enough to leave artefacts on the camera film. I don’t know exactly what sort of radiation dose is required to effect a piece of photochemical film (Remember that stuff, that was used before digital photography?), but I really expect it to show some damage under these conditions.

0:44:45

If you’ve got documentary evidence of these lives lost as a direct result of the disaster, that don’t appear in any of the UN’s findings, then I’m sure the UN would love to hear about it.

0:52:30

Oh dear - it’s “imagined” health physics, romanticised Hollywood fiction style.

“It finds a way in, and knocks you out”.

1:03:00 or thereabouts:

7000 R/hr - and still no effect on the video camera film. I wonder how strong the ionising radiation field needs to be to affect it?

1:12:30 -

“…The visit stirs up painful memories. He was fatally exposed to radiation during the seven months he spent covering the battle. Since then, he’s had to be hospitalised for over two months each year.”

He was fatally exposed to radiation? Oh, really? So you’re reanimated a dead man to interview for the program?

Chernobyl showed us the true nature of nuclear energy in human hands

No, Chernobyl showed us the potential for folly associated with the Soviet way of doing things back then. Keep in mind that the non-Soviet world has never even come remotely close to experiencing such an accident.

1:31:20:

“Inside, there are 100 kilograms of plutonium.

One microgram is a lethal dose for a human being. That means there is enough plutonium to poison 100 million people.”

Even assuming that “one microgram of plutonium is a lethal dose for a human being”, which it isn’t, I expect that somebody who is really a nuclear physicist should know how to count, and not allow such a glaring error of arithmetic to go uncorrected.

“The half-life of plutonium is 245,000 years.”

In order of descending half-life:

Pu-244: 80 million years

Pu-242: 373,300 years

Pu-239: 24,100 years

Pu-240: 6564 years

Pu-238: 87.7 years

Pu-241: 14.35 years

Pu-236: 2.858 years

The nuclides bolded are the most common ones. I don’t know about you, but Iexpect someone who is a nuclear physicist to get that right, and not just pull some nonsense number out of thin air! Again, not one of these plutonium nuclides has the half-life claimed in the film. What’s more, no credible nuclear physicist would state that “the half-life of plutonium is such-and-such” without specifying which nuclide he was talking about.

But wait - if you’ve watched the video, there are a couple more scenes that you almost certainly haven’t overlooked:

“Yet, it is thanks to these men that the worst was avoided. A second explosion, ten times more powerful than Hiroshima, which would have wiped out half of Europe.”

Yes, you heard that correctly. They claim that a  150 kiloton nuclear detonation could have happened. See below, for what I think of that.

0:34:00 - 0:35:00

The ensuing chain reaction could set off an explosion, comparable to a gigantic atomic bomb.

“Our experts studied the possibility, and concluded that the explosion would have had a force of three to five megatons. Minsk, which is 320 kilometres from Chernobyl, would have been razed, and Europe rendered uninhabitable.”

A 3 to 5 megaton nuclear detonation.

I apologise for putting this bluntly, but there’s only one thing I can say to that. What complete and utter bullshit.

They trump out the nuclear weapon explosion stock footage and everything. This is quite possibly the most blatantly shameless, ridiculous, completely falsifiable and utterly ridiculous example of shameless and absurd anti-nuclear-power propaganda I have ever seen.

Posted in Chernobyl, anti-nuclear activism, health physics | Tagged: , , | 16 Comments »

Anti-nuclear quote of the week.

Posted by Luke Weston on April 18, 2008

“Every year Areva, the French conglomerate that handles reprocessing, dumps so much radioactive liquid into the Channel that, says Lochbaum of the Union of Concerned Scientists, “there are certain beaches where the effluent pipe is where you can get a suntan at night.”"

[source]

What absolutely laughable, ridiculous nonsense. Hell, even Caldicott probably wouldn’t be that stupid. Lochbaum does know what a suntan is, and what causes it, right?

Posted in David Lochbaum, Helen Caldicott, anti-nuclear ignorance, anti-nuclear quote of the week, health physics, radiation | Tagged: , , , , , | 2 Comments »

Bioconcentration and biomagnification of radionuclides of biochemically-significant elements.

Posted by Luke Weston on March 17, 2008

 Anti-nuclear-energy activists often talk about the potential for biomagnification of radioactive nuclides in the environment as the consequence of any, even extremely dilute, releases of such radionuclides into the environment.

Consider the following claims, typical of such views, for example:

“Tritium is also more dangerous when it becomes organically bound in molecules of food. As such it is incorporated into molecules, including DNA within bodily cells. Chronic exposure to contaminated food causes 10% of the tritium to become organically bound within the body where it has a biological half-life of 21 to 550 days meaning that it can reside in the body from one to twenty-five years.”

“When tritium is released to the environment, it is taken up by plants and trees, partially incorporating into the ecosystem. Trees constantly transpire water vapor into the air; it has been found that higher concentrations of tritium occur at night at breathing height in a forest that has incorporated tritium from a nearby reactor.”

(Extracts from Nuclear Power is Not the Answer) 

So, does bioconcentration of tritium in the food chain occur?

Bioconcentration or biomagnification of tritium in the form of tritiated water in biological systems does not occur at all, although it can occur with some other radionuclides. This is due, in part, to the relatively small biological half-life for water in biological systems, and the large concentration of light water in the environment, which results in massive isotopic dilution of tritium entering the ecosphere. Tritium is simply hydrogen, and your body cannot tell one hydrogen atom from the next - whilst large volumes of water are constantly being taken into the body, and passed out of the body, the total amount of hydrogen within ones body remains essentially constant, as is also the case for the various other chemical elements which make up the human body.

Biomagnification is the buildup of certain chemical pollutants in the bodies of organisms at higher trophic levels of food webs - the bioaccumulation of a substance up the food chain by transfer of residues of the substance in smaller organisms that are food for larger organisms in the food web. It generally refers to the sequence of processes that results in higher concentrations in organisms at a higher trophic level - further “up the food chain”. Organisms at lower trophic levels accumulate small amounts. Organisms at the next higher level eat many of these lower-level organisms and hence accumulate larger amounts. These processes result in an organism having higher concentrations of a substance than is present in the organisms prey or food. Biomagnification can result in higher concentrations of the substance than would be expected if water were the only exposure mechanism. Accumulation of a substance only through contact with water is known as bioconcentration.

Bioaccumulation is a general term for the accumulation of such substances in an organism or part of an organism. The process of bioaccumulation involves the biological sequestering of substances that enter the organism through respiration, food intake and/or other routes of absorbtion of the substance. Such sequestering results in the organism having a higher concentration of the substance than the concentration in the organisms surrounding environment. The level at which a given substance is bioaccumulated depends on the rate of uptake, the route of uptake, how quickly the substance is eliminated from the organism, transformation of the substance by metabolic processes, the lipid (fat) content of the organism, the hydrophobicity of the substance, environmental factors, and other biological and physical factors. As a general rule the more hydrophobic a substance is the more likely it is to bioaccumulate in organisms, such as fish. Increasing hydrophobicity (lipophilicity) leads to an increasing propensity towards bioaccumulation.

A related term is bioconcentration. Bioconcentration is a process that results in an organism having a higher concentration of a substance than is in its surrounding environmental media, such as stream water. Bioconcentration differs from bioaccumulation because it refers only to the uptake of substances into the organism from water alone. Bioaccumlation is the more general term because it includes all means of uptake into the organism.

Biomagnification, or bioamplification, occurs within a trophic level, and is the increase in concentration of a substance in an organisms tissues due to uptake from food and sediments in an aquatic milieu, wheras bioconcentration is defined as occurring when uptake from the environment is greater than the rate of excretion. Where bioaccumulation refers to how pollutants enter a food chain; biomagnification refers to the tendency of pollutants to concentrate as they move from one trophic level to the next, up the “food chain.” Whilst bioaccumulation refers to an increase in concentration of a pollutant from the environment to the first organism in a food chain, biomagnification refers to an increase in concentration of a pollutant from one link in the food chain to another.
We are traditionally concerned about these phenomena because together they mean that even small concentrations of toxic substances in the environment can find their way into organisms in high enough dosages to cause problems. In order for biomagnification to occur, the pollutant must be long lived, fat-soluble, mobile, and biologically active - i.e. toxic. If a pollutant is short-lived, it will be broken down before it can become dangerous. If it is not mobile, it will stay in one place and is unlikely to be taken up by organisms. If the pollutant is soluble in water it will be excreted by the organism. Pollutants that dissolve in fats, however, may be retained for a long time. Lipid soluble (lipophilic) substances cannot be excreted in urine, an aqueous solution, and so accumulate in fatty tissues of an organism if the organism lacks enzymes to degrade them. When eaten by another organism, fats are absorbed in the gut, carrying the substance, which then accumulates in the fats of the predator. Since at each trophic level of the food chain there is an energy loss, a predator must consume lots of prey, and therefore consumes significantly larger amounts of any biomagnifying lipophilic substance consumed by the prey organism.

There are two main groups of toxic substances that that are subject to biomagnification - toxic metals and persistent halogenated organic compounds. Both are lipophilic and not easily degraded. Novel organic substances are not easily degraded because organisms lack previous exposure and have thus not evolved specific detoxification and excretion mechanisms, as there has been no selection pressure from them. These substances are consequently known as persistent organic pollutants, and include the synthetic organic chlorine compounds which are today well-known for their potential for biomagnification and environmental harm, such as the insecticide DDT.

Heavy metals are chemically stable because they are chemical elements, and therefore cannot be destroyed or converted into a non-toxic form. (Except for the case of a radioactive metal, which will change into a differerent chemical element when it undergoes radioactive decay.) Organisms, particularly those subject to naturally high levels of exposure to metals, have mechanisms to sequester and excrete metals. Problems arise when organisms are exposed to higher concentrations than usual, which they cannot excrete rapidly enough to prevent damage. These metals are transferred in an organic form.

A classic example of a toxic heavy metal is mercury, which forms organic species such as methylmercury, which is lipid soluble, and can easily biomagnify in environmental systems. Other toxic transition metals - the so-called “heavy metals” - can be subject to biomagnification to some degree, too - for example, the toxic metal cadmium. Since biochemical behavior is independent of what the isotopic composition of the metal is, a radionuclide, such as the low-yield fission product \mathrm{^{113m}Cd}, perhaps, is subject to a potential for biomagnification just like any other cadmium. For example, though mercury is only present in small amounts in seawater, it is absorbed by algae, generally as methylmercury. It is efficiently absorbed, but only very slowly excreted by organisms. Bioaccumulation and biomagnification result in buildup in the adipose tissue of successive trophic levels: zooplankton, small nekton, larger fish etc. Anything which eats these fish also consumes the higher level of mercury the fish have accumulated. This process explains why predatory fish such as swordfish and sharks or birds like osprey and eagles have higher concentrations of mercury in their tissue than could be accounted for by direct exposure alone. For example, herring contains mercury at approximately 0.01 ppm and shark contains mercury at greater than 1 ppm.

Now, let’s talk about radionuclides. radioactive nuclides such as, say, hydrogen-3, carbon-14, iodine-131 or strontium-90, for example, can certainly be uptaken by living organisms - including, but not limited to, humans. Tritium (hydrogen-3) is almost always present in the environment in the form of water - and, of course, every living thing uptakes water from its environment, so, if there is \mathrm{^{3}H} present in the water - keep in mind that all water has some naturally occurring \mathrm{^{3}H} in it - then \mathrm{^{3}H} will be absorbed by the organism. Now, remember - it is just hydrogen.

The biochemistry of cells does not care in the slightest what nuclide a particular atom of hydrogen or a particular element is - it is only concerned with the chemistry of the material. Therefore, the \mathrm{^{3}H} will be used by the cells of the organism, and incorporated into tissues and biomolecules along with every other hydrogen atom that the organism has uptaken. Since an atom of tritium is just another hydrogen atom, of course it is exchanged into and incorporated into some hydrogen-containing biomolecules - in other words, just about any organic molecule found in a biological system. However, water is constantly being excreted from living systems as well as constantly being uptaken - a cell of Escherichia coli contains 70% water by mass, a human body 60-70%, plant tissue up to 90% and the body of an adult jellyfish is made up of 94 to 98% water. Now, the proportion of water in an organism such as these is constant - except for a small difference due to the growth of the organism, the rate of water uptake into an organism is equal to the rate of water excretion, and whilst hydrogen - which could be \mathrm{^{1}H}, \mathrm{^{2}H} or \mathrm{^{3}H}, it doesn’t matter - is constantly being moved between water molecules and more complex biomolecules, and it is constantly being excreted - both in the form of water and in the form of more complex biomolecules.

However, some tritium taken up into the body could be incorporated into a biomolecule in the tissues of the body, and it could remain there for some time - but as more stable hydrogen is constantly being exchanged through the body in large quantities, the concentration of tritium within the body from any given intake will decay exponentially, just as the metabolism and excretion of, say, a drug taken into the body follows an exponential decay law - hence, we speak of the biological half-life.

The overall amount of hydrogen per unit mass of a living organism is essentially constant. If there is a constant environmental source of a radionuclide such as tritium - such as the natural cosmogenic formation of tritium - then the overall amount of tritium per unit mass of a living organism is essentially constant.

Exactly the same argument applies to radionuclides of other biologically active elements - like, say, carbon-14. \mathrm{^{14}C} is constantly uptaken from the atmosphere by plants in the form of \mathrm{^{14}CO_{2}}, and incorporated into the organic biomolecules within the tissues of the plant as the plant grows - and when an animal eats the plant, the \mathrm{^{14}C}-containing biomolecules are metabolised by the animal. As with hydrogen nuclides, the \mathrm{^{14}C} is constantly being turned over between living systems and the ecosphere, as organic compounds are excreted by the animals - for example in the exhalation of \mathrm{^{14}CO_{2}}. Again, the overall concentration of \mathrm{^{14}C} within the tissues of a living system is held constant - this is how carbon-14 dating works! If the concentration of \mathrm{^{14}C} within a living organism wasn’t constant, then obviously \mathrm{^{14}C}-dating of once-living materials would be impossible.

The same arguments apply to, say, strontium, or iodine - whilst a radionuclide such as strontium-90 certainly can be uptaken into the human (or animal) body, and can be used in osteogenesis and incorporated into bone because of the chemical similarity between \mathrm{Sr^{2+}} and \mathrm{Ca^{2+}}, the overall concentration of calcium - calcium and strontium combined, for that matter - within the body is maintained at a certain static level. When iodine - some of which could be contaminated with, say, radioactive iodine-131 - is uptaken by the body, iodide ions are used by the thyroid gland in the biosynthesis of the iodine-containing thyroid hormones, thyroxine and triiodothyronine. But, of course, the concentration of thyroxine and triiodothyronine in the blood is kept around a fairly homeostatic value - whilst some iodine is essential for the biosynthesis of these hormones and is thus essential for health, it does not accumulate arbitrarily in the body, either in the form of the iodine-containing hormones or as free iodide ion.

Obviously we know that such chemical elements - radionuclides or not - are uptaken extensively by biological systems; but that is not the same thing as biomagnification - do they bioaccumulate or biomagnify?

Clearly, they do not.
It has in fact been determined empirically in Perch Lake in Canada that there is a progressive decline in the concentration of cobalt-60 and strontium-90 as they are transferred to higher trophic levels. In other words, predators, such as carnivorous fish, have lower concentrations of cobalt-60 and strontium-90 per unit body weight than do forage fish, insects and plants, as a result of biological discrimination against uptake of these elements of limited biochemical usefulness. It is now generally agreed that the same principle is valid for most other radionuclides, with a few exceptions, such as tritium, soluble potassium-40 (which occurs naturally, not as a result of anthropogenic nuclear technology), and caesium-137, which is a chemical analog of potassium, which are incorporated without biodiscrimination into all living organisms. Most radionuclides are not subject to biomagnification up the food chain, thus differing them from organic pollutants such as DDT. This is of significant importance in the assessment of radioactive  releases into the environment.

Editor’s note: As you may note, I’ve just discovered WordPress’s built-in LaTeX engine. Unfortunately, it looks a little bit awkward in the above post, as you can see, with the TeX-formatted text much bigger than the surrounding text. I’ll have to see if there’s a way around that in future.

Posted in environment, environmental science, health physics, nuclear power, radioactive waste, radionuclides in the environment | Tagged: , , , , | No Comments »

Kentucky senator pushing for fair consideration of nuclear energy

Posted by Luke Weston on March 13, 2008

Atomic Insights reports that Kentucky state Senator Bob Leeper has been doing some reading and listening lately about the coming of a new wave of nuclear plant construction, and he is working to position his state as a potential site for consideration. He has recently introduced a bill that would change the language in the law to allow licensed on site storage as a means of safely handling the byproducts that remain after using fuel in a reactor for a period of time, as compared with current Kentucky law which precludes the construction of a new nuclear power plant until there is a licensed and available location for permanent disposal of used nuclear fuel or the radioactive waste which may be left following recycling of such used fuel, such as the Yucca Mountain facility under development in the United States.

Of course, some people, such as Joseph Mangano, executive director of the Radiation and Public Health Project, a name that those with their finger on the pulse of nuclear energy policy in the United States and elsewhere will have heard before, has other ideas:

 “One problem with nuclear reactors is what to do with the high-level waste they produce. This waste is actually a cocktail of chemicals such as Cesium-137, Iodine-129, Strontium-90 and Plutonium-239, each radioactive and cancer-causing.”

There’s no way that it is appropriate to call these kinds of materials waste -  they are radionuclides with useful and important technological, scientific and industrial applications. Of course, if we greatly expand the use of nuclear fission as an energy source throughout the world, along with the recycling and efficient re-use of the materials contained within irradiated nuclear fuels, it is likely that the inventories of such fission products thus created will ultimately dwarf demand for some of these radioactive materials - and it could be decided that these surplus quantities might be moved to deep underground storage, either for very long term storage, or permanant disposal.

“The waste decays slowly, remaining in dangerous amounts for thousands of years, and must be kept from escaping into the air, water and food supply”

Relatively short lived fission products, such as caesium-137 and strontium-90, with half-lives of 30 years and 29 years respectively, must be isolated from the environment for around 300 years, not thousands of years.

Longer lived fission products, such as iodine-129, one of the very longest lived of the fission product nuclides, can have half-lives of millions of years - with correspondingly smaller specific activities, and in most cases, much smaller nuclear fission yields. Some such long-lived fission products, such as I-129 and technetium-99, have sufficiently large neutron capture cross sections such that destruction of the radioactive nuclide by way of nuclear transmutation in a nuclear reactor is feasable.

I get especially bothered when these people talk of plutonium-239 and “waste” in the same sentence - it is one of the most potent, most energy dense, and most useful fuels known to humankind. There is absolutely no way that it should ever be thought of as “waste”, and it should not be wasted.

 “Another potential health problem is a large-scale release of radioactivity from a meltdown. Accidents have occurred at several reactors, including the 1986 total meltdown at Chernobyl and the 1979 partial meltdown at Three Mile Island. But in addition to accidents, a terrorist attack could also cause a meltdown. Safe evacuation would be impossible, and local residents would be exposed to toxic radiation, causing many thousands to suffer from radiation poisoning and cancer.”

The Chernobyl disaster was not a meltdown in the usual sense of the term - it was a disaster triggered by complete destruction of the reactor core caused by a massive, explosive power excursion and steam explosion, not a fuel damage accident caused by a loss of coolant accident.

 The design, operation and physical characteristics of the RBMK power reactors at Chernobyl during the era of the Soviets have absolutely nothing  to do with the operation of the commercial nuclear power industry in the world today. The Chernobyl disaster is absolutely irrelevant, it has absolutely no relevance at all, to the use of light water reactors in the commercial nuclear power industry in the United States today.

No accident even remotely comparable to the Chernobyl accident, which, in the absence of any kind of real containment around the nuclear reactor, spewed radioactivity from the destroyed reactor core for thousands of miles, has ever occured in the commercial nuclear power industry in the Western world.

At Three Mile Island, where a loss of coolant accident and partial meltdown occurred in 1979,  was safe evacuation impossible? Were local residents exposed to “toxic radiation”? What dose of ionizing radiation did they receive? This was what is usually claimed as the most dangerous nuclear power reactor accident ever in the United States - did it cause “many thousands to suffer from radiation poisoning and cancer”? Did it harm anyone?

“Although it has never had a nuclear power reactor, Kentucky is no newcomer to nuclear plants. The Paducah Gaseous Diffusion Plant has been enriching uranium for nuclear weapons and reactors since 1952 — and contaminating the local environment for decades.”

 Does the USEC Paducah plant produce HEU for nuclear weapons applications? That’s an open question to my readers - I’d like to know the answer.

What evidence, is there, that Paducah has been “contaminating the local environment for decades“? Is there any evidence of health or ecological effects on the surrounding community?

Local residents have breathed, drunk or eaten these contaminants, and they may have suffered. In the past quarter century, the death rate in the four closest counties (Ballard and McCracken in Kentucky, Massac and Pulaski in Illinois) is about 9 percent above the U.S. rate for both whites and blacks. This amounts to nearly 3,000 “excess” deaths in a population of only 95,000. The four counties have no obvious health risk, like language barriers, lack of education or extreme poverty, so Paducah must be considered as a potential factor in these high rates.

Kentucky already has the highest cancer death rate of any state in the nation. There is no need to increase cancer risk by introducing a hazardous means of producing electricity.

Has any scientific, peer-reviewed, epidemiological study of  health, death and disease, and the aetiology of any such abnormalities, in these counties ever been performed?

Is there any evidence, peer-reviewed scientific evidence of any kind, that nuclear energy is a “hazardous means of producing electricity” which “increases cancer risk”?

 

 

 

Posted in Joseph Mangano, Kentucky, Paducah, anti-nuclear activism, health physics, nuclear power, nuclear safety, radioactive waste | Tagged: , , , , , , , | 6 Comments »

Depleted uranium… for dinner!

Posted by Luke Weston on March 8, 2008

 This isn’t about nuclear energy, strictly speaking - but I still think it’s worth spreading.

“Dr. Buzzo”, the blogger behind the “Bad Science” blog Depleted Cranium - has recently published a great little video on YouTube:

“Not long ago I noticed that during some flaming and name-calling on the the anti-depleted uranium crowed stated that “If you love depleted uranium so much why don’t you have it for dinner.”

http://www.youtube.com/watch?v=qk9vHQrKMdk

The YouTube video is pretty self explanatory - go check it out!

Posted in bad science, depleted uranium, health physics | Tagged: , , | No Comments »