Friday, April 13, 2007
Texas A&M Fails to Report Stricken Student in Bioweapons Lab for 14 Months
TEXAS A&M FAILED TO REPORT STUDENT STRICKEN WITH BRUCELLA DURING BIOWEAPONS EXPERIMENT
By Sherwood Ross
Texas A&M University failed to report in a timely manner to Federal authorities that a biology student was stricken with the dangerous brucella pathogen in its College Station laboratory for bioweapons agent research on February 9th of 2006. The university made its disclosure this April 10th, 14 months later, and only after insistent prodding by the Sunshine Project, an Austin, Tex.-based arms control watchdog organization.
Under Federal law, such incidents are supposed to be reported within seven days to the Centers For Disease Control and Prevention.
The student was seriously ill for several months with brucellosis but recovered. The disease is believed to kill between two to three percent of those it infects. The student, whose name and gender has not been disclosed by Texas A&M to Sunshine, apparently came down with the disease, also known as undulant fever, attempting to clean what is called a Madison Aerosol Chamber(MAC) where mice had been exposed to aerosolized brucella particles.
The accident occurred under the supervision of Texas A&M professor David McMurray, inventor of the (MAC). According to Sunshine, the case of the stricken student is the third report of a serious illness in connection with the chamber’s use. On one occasion, a leaky aerosol chamber was responsible for three tuberculosis infections in a Seattle lab in 2004.
The MAC is used to infect animals with disease through their lungs. Cultures of the organisms causing tuberculosis, or the bioweapons agents brucella, anthrax, or Q fever, are placed in the MAC’s nebulizer, which mixes them with the air. The resulting aerosol is directed into a metal chamber in which animals placed on racks breathe in the agent.
The Texas A&M work is being funded by the Department of Homeland Security(DHS) and the National Institutes of Health(NIH).Texas A&M’s professor Thomas Ficht is the Principal Investigator.
E-mails that Texas A&M finally released to Sunshine late on Tuesday night (April 10) reveal the University broke federal law by not reporting the infection, Sunshine’s Edward Hammond said. The Select Agent Rule required A&M to report the infection immediately upon its discovery and for the school to file a formal report, called APHIS/CDC Form 3, within 7 days. Failure to do so means Texas A&M could face fines of up to $750,000 and lose Federal funding for its research.
Asked if the university had delayed reporting the accident, Ficht replied, “I’m not supposed to talk to anybody about that, not now,” and referred this reporter to a school public relations official. Ficht is well known in his field and holds both a 2000 Pfizer Research Award and a 2004 Sigma Xi Research Award.
In recent years, Texas A&M has received between $284,000 and $363,000 annually from the NIH just for brucella research, Hammond said, but the overall NIH funding is “much higher.” How much Texas A&M gets from DHS is not known.
“The evidence released to us indicates that Texas A&M officials discussed the federal requirement to report the incident, yet they did not do so,” Hammond said. “They chose to ignore the law, and that irresponsible decision to endanger public health and security should be swiftly and severely punished with maximum fines and loss of federal research funding.”
In refusing to provide information about the infection, Texas A&M officials also flouted the Texas Public Information Act, Hammond said. He said Sunshine is filing a complaint with Texas Attorney General Greg Abbott that may result in other fines and/or jail sentences if school officials are found guilty of hiding documents. Sunshine obtained its information from the school only after formally requesting records under the Texas Public Information Act.
In recent years, several Texas universities, including Texas A&M, have attempted to conceal their biological laboratory work from public scrutiny. According to Sunshine, the universities of Texas at Arlington and San Antonio and the University of Texas Southwestern at Dallas are obligated under NIH guidelines to have their internal oversight committees report on their biological lab work to NIH but declined to do so. And Texas A&M’s oversight committee did not report the brucella episode, Hammond said.
The work of the Texas universities, like that of approximately 400 other Federally-funded labs across the nation, may involve pathogens that could possibly be used for offensive germ warfare, banned by the 1972 Biological and Toxic Weapons Convention(BTWC), which the U.S. signed. It prohibits “development, production, stockpiling, and use of microbes or their poisonous byproducts except in amounts necessary for protective and peaceful research.”
According to Professor Francis A. Boyle, an international legal expert at the University of Illinois at Champaign, “Aerosolization and an aerosol chamber are a classic tip-off for the prohibited research, development and testing of an offensive biological weapon in violation of the (BTWC) and its U.S. domestic implementing legislation, the Biological Weapons Anti-Terrorism Act of 1989, which provides for life in prison.” Boyle wrote the 1989 Act, passed unanimously by both Houses of Congress. He is also author of “Biowarfare and Terrorism,” published by Clarity Press.
Since 9/11, the Bush Administration has spent tens of billions of dollars on bioweapons research. The sum may be $40-billion or higher, but an accurate figure is not available as much of the work is being conducted in secret.
Some universities have leaped at the opportunity for
Federal funding for such research from NIH and DHS. Hammond claims, “Government and academic labs are responding less to bona fide needs than the urge to build power and revenue centers for what they hope is a perpetual biodefense boom. This will result in a dangerous proliferation of bioweapons agents and the knowledge to use them.”
He noted the U.S. is facing a virulent new strain of drug-resistant gonorrhea. Unfortunately, he added, “the NIH has been extravagantly funding research into ‘threat’ diseases like glanders, which has not been seen in humans in the U.S. since the 1940s except, of course, lab-acquired infections in biodefense facilities. What a shame.”
The lack of transparency in U.S. federally-funded biological laboratories has been a growing cause for concern. Jackie Cabasso, of the Western States Legal Foundation of Oakland, Calif., said, “the U.S. is now massively expanding its biodefense program, mostly in secretive facilities. Other countries are going to be suspicious. This bodes badly for the future of biological weapons control.”
According to Jonathan King, professor of molecular biology at MIT, “the Bush administration launched a major (biological weapons) program which threatens to put the health of our people at far greater risk than the hazard to which they claimed to have been responding.” Bush’s policies, he continued, “do not increase the security of the American people. They bring new risk to our population of the most appalling kind.”
Sherwood Ross is a reporter who has worked for major dailies and wire services. Reach him at sherwoodr1@yahoo.com
Wednesday, December 20, 2006
Bush developing illegal bioterror weapons
Sherwood Ross
Middle East Times
December 19, 2006
WASHINGTON -- In violation of the US Code and international law, the Bush administration is illegally developing offensive germ warfare capabilities on an unprecedented scale. In fact, it is spending more on such weapons (in inflation-adjusted dollars) than the $2 billion spent on the "Manhattan Project" that made the atomic bomb in World War II.
So says Francis Boyle, the professor of international law who drafted the Biological Weapons Anti-Terrorism Act of 1989 enacted by Congress. He states the Pentagon "is now gearing up to fight and 'win' biological warfare" pursuant to two Bush national strategy directives adopted without "public knowledge and review" in 2002.
The Pentagon's Chemical and Biological Defense Program was revised in 2003 to implement those directives, endorsing "first-use" strike of chemical and biological weapons (CBW) in war, says Boyle, who teaches at the University of Illinois, Champaign.
Terming the action "the proverbial smoking gun," Boyle said the mission of the controversial CBW program "has been altered to permit development of offensive capability in chemical and biological weapons!"
The same directives, Boyle writes in his book Biowarfare and Terrorism, "unconstitutionally usurp and nullify the right and the power of the United States Congress to declare war in gross and blatant violation of Article 1, Section 8, Clause 11 of the United States Constitution."
For fiscal years 2001-04, the Federal government funded $14.5 billion "for ostensibly 'civilian' biowarfare-related work alone," a "truly staggering" sum, Boyle wrote. Another $5.6 billion was voted for "the deceptively-named 'Project BioShield,'" under which Homeland Security is stockpiling vaccines and drugs to fight anthrax, smallpox, and other bioterror agents, Boyle wrote. Protection of the civilian population is, he said, "one of the fundamental requirements for effectively waging biowarfare."
The Washington Post reported December 12 both houses of Congress this month passed legislation "considered by many to be an effort to salvage the two-year-old Project BioShield, which has been marked by delays and operational problems." When President Bush signs it, the law will allocate $1 billion more over three years for new research "to pump more money into the private sector sooner."
"The enormous amounts of money" purportedly dedicated to "civilian defense" that is now "dramatically and increasingly" being spent, Boyle writes, "betrays this administration's effort to be able to embark on offensive campaigns using biowarfare."
Boyle said Federal spending has co-opted and diverted the US biotech industry to biowarfare, pouring huge sums into university and private sector laboratories. According to Rutgers University molecular biologist Richard Ebright, over 300 scientific institutions and 12,000 individuals today have access to pathogens suitable for biowarfare and terrorism. At the same time, Ebright found, the number of grants by the National Institute of Health to research infectious diseases with biowarfare potential has shot up from 33 in the 1995 to 2000 period to 497.
Academic biowarfare participation involving the abuse of DNA genetic engineering since the late 1980s has become "patently obvious," Boyle said. "American universities have a long history of willingly permitting their research agendas, researchers, institutes, and laboratories to be co-opted, corrupted, and perverted by the Pentagon and the CIA."
He continued, "These despicable death-scientists were arming the Pentagon with the component units necessary to produce a massive array of DNA genetically engineered biological weapons."
In a forward to Boyle's book, Jonathan King, a professor of molecular biology at Massachusetts Institute of Technology, wrote "the growing bioterror programs represent a significant emerging danger to our own population" and "threatens international relations among nations." King said that while such programs "are always called defensive," in fact, "with biological weapons, defensive, and offensive programs overlap almost completely."
The US is "in breach" of the Biological Weapons Convention, the Chemical Weapons Convention, and US domestic criminal law, Boyle writes. In February 2003, for example, the US granted itself a patent on an illegal long-range biological weapons grenade.
Boyle said other countries grasp the military implications of US germ warfare actions and will respond in kind. "The world will soon witness a de facto biological arms race among the major biotech states under the guise of 'defense,' and despite the requirements of the Biological Warfare Convention."
"The massive proliferation of biowarfare technology, facilities, as well as trained scientists and technicians all over the United States courtesy of the neocon Bush Jr. administration will render a catastrophic biowarfare or bioterrorist incident or accident a statistical certainty," Boyle warned.
Sherwood Ross is a Virginia-based freelance writer on political and military issues
Friday, December 15, 2006
US Government Biological Weapons Legislator Says 2001 Anthrax Attacks Part Of Government Bio-warfare Program
Expert says FBI covered up the plot to attack Congress which may have been perpetrated by the same people who carried out the 9/11 attacks
Steve Watson, Infowars.net
Wednesday, December 13, 2006
The real culprits behind the 2001 anthrax attack on Congress were most likely US government scientists at the army's Ft. Detrick, MD., bioterrorism lab according to a former government biological weapons legislator and University of Illinois Professor.
Dr Franics A. Boyle says the FBI covered up these facts and has also quite clearly stated that he doubts the official government story that 19 arabs with boxcutters perpetrated the attacks of 9/11.
Boyle is a leading American professor, practitioner and advocate of international law. He was responsible for drafting the Biological Weapons Anti-Terrorism Act of 1989, the American implementing legislation for the 1972 Biological Weapons Convention. He served on the Board of Directors of Amnesty International (1988-1992), and represented Bosnia- Herzegovina at the World Court. Professor Boyle teaches international law at the University of Illinois, Champaign. He holds a Doctor of Law Magna Cum Laude as well as a Ph.D. in Political Science, both from Harvard University.
"I believe the FBI knows exactly who was behind these terrorist anthrax attacks upon the United States Congress in the Fall of 2001, and that the culprits were US government-related scientists involved in a criminal US government bio-warfare program," Boyle says in his new book Biowarfare and Terrorism.
Only a "handful" of scientists had the means to carry out the attack, yet the FBI ordered the destruction of the anthrax culture collection at Ames, IA., from which the Ft. Detrick lab got its pathogens. Boyle states that only top level scientists with access to "moonsuits" that enabled them to safely process and manufacture super-weapons-grade anthrax could have carried out the attacks.
"The trail of genetic evidence would have led directly back to a secret but officially-sponsored US government biowarfare program that was illegal and criminal" , Boyle said. However, impartial scientists were not allowed to perform genetic reconstruction of the anthrax found in letters mailed to Senators Daschle (D-S.D.) and Patrick Leahy, (D -Vt.) in late 2001.
We have previously exposed how leading members of the Bush administration and White House staff were on the anthrax-treating antibiotic Cipro up to six weeks before the attacks occurred. It is also documented that the anthrax strain used was military grade. This was widely reported in 2002 in publications such as the New Scientist. However, this fact has recently been totally changed with the FBI now suggesting that common anthrax, not military grade anthrax was used.
The whole thing "appears to be a cover-up orchestrated by the FBI." according to Dr Boyle.
Boyle goes on to inquire, "Could the real culprits behind the terrorist attacks on 11 September 2001, and the immediately following terrorist anthrax attacks upon Congress ultimately prove to be the same people? Could it truly be coincidental that two of the primary intended victims of the terrorist anthrax attacks - Senators Daschle and Leahy - were holding up the speedy passage of the pre-planned USA Patriot Act ... an act which provided the federal government with unprecedented powers in relation to US citizens and institutions?"
Clearly Dr Boyle has a hard time believing what the government says happened on 9/11.
The anthrax attacks cleverly (or coincidentally if you choose to believe) coincided with the terrorist atrocities and sent Congress into shut down for days. Immediately after re-convening the liberty smashing PATRIOT Act was passed without even being read by members.
In addition, the Bush administration moved to begin planning a major $10 billion expansion of the bioweapons labs at Fort Detrick. Residents in the area have fiercely campaigned against the expansion.
In a forward to Boyle's book, Dr. Jonathan King, Professor of Molecular Biology at M.I.T. and a founder of the Council for Responsible Genetics, says the government's "growing bioterror programs represent a significant emerging danger to our own population."
Those who cannot fathom how or why the government could kill almost 3000 citizens, including police and firefighters, on 9/11 need look no further than the anthrax attacks, which provide solid proof that criminal elements within the structure of authority are in operation and don't give a damn about who they kill to achieve their goals of social control.
There are countless examples of the US government having illegally tested and used bio-weapons on its own citizens. The Tuskegee Syphilis Study, The Program F fluoride study, Project SHAD which we are now learning used live toxins and chemical poisons on American servicemen on American soil, spraying clouds of bacteria over San Francisco, releasing toxic gases into the New York subway, holding open-air biological and chemical weapons tests in at least four states in the 1960s, the list goes on.
The Pentagon's biowarfare program has long been in operation and US citizens have never been spared from experimentation. To get more of a taste for just how hideous the secret biowarfare program is, click here and go to Rense.com, which has a lengthy (but by no means a comprehensive) list of previous known bio-experiments conducted on the population by the criminal elite.
Monday, December 4, 2006
US and Israel Targeting DNA in Gaza? The DIME Bomb: Yet another genotoxic weapon
December 04 2006
By James Brooks
Part 1 of 3
It’s been almost five months since the first report that Israeli drone aircraft have been dropping a “mystery weapon” on Palestinians in the Gaza Strip. Since then, news media around the world have run stories depicting the strange and “horrific” wounds inflicted by the new bomb. The international press has spoken with Palestinian doctors and medics who say Israel’s new device is a kind of chemical weapon that has significantly increased the fatality rate among the victims of Israeli attacks. [1][2]
In mid-October, Italian investigators reported forensic evidence that suggests the new weapon may also represent the near future of US “counterinsurgency warfare”. Combined with photographs of the victims and testimony from attending doctors, this evidence points to the use of Dense Inert Metal Explosives (DIME). [3]
DIME is an LCD (“low collateral damage”) weapon developed at the US Air Force Research Laboratory. Publicly, it is slated for initial deployment in 2008. DIME bombs produce an unusually powerful blast within a relatively small area, spraying a superheated “micro-shrapnel” of powdered Heavy Metal Tungsten Alloy (HMTA). Scientific studies have found that HMTA is chemically toxic, damages the immune system, rapidly causes cancer, and attacks DNA (genotoxic).[4-11]
It is unfortunate that the US media have virtually blacked out the story of Israel’s new weapon, not least because our own military may soon be using it in Iraq and Afghanistan. The story might also have told us something about the grossly disproportionate brutality of Israel’s war on the Palestinian people—reason enough for the media to suppress it. [12]
Thanks to the intrepid Italians, the story could even have introduced Americans to their government’s DIME weapons program. This three-part article will ask whether Israel is ‘testing’ US DIME bombs in the Gaza Strip, and explore the workings, dangers, and projected use of DIME weapons and their roots in depleted uranium (DU) research. These parallels will lead us to consider DIME in its historical context, as the latest innovation in the US military’s long-running development of genotoxic weapons.
“They cannot return to life again”
The first reports about ‘Israel’s new weapon’ came from Dr Joma Al-Saqqa, chief of the emergency unit at Gaza’s largest hospital, Al-Shifa. Dr. Al-Saqqa said that Israel was using “a new ‘chemical’ weapon” and its siege was “a live exercise on a new ammunition that, so far, has resulted in killing 50 Palestinians and injuring 200.” He observed that, “despite the damage in internal soft tissue in the bodies of injured people, the fragments were not detected by X-ray. In other words, they had disappeared or dissolved inside the body.”[13]
“There were usually entry and exit wounds,” Dr. Al-Saqqa reported. “When the wounds were explored no foreign material was found. There was tissue death, the extent of which was diff icult to determine….A higher deep infection rate resulted with subsequent amputation. In spite of amputation there was a higher mortality.” The effects of the weapon seemed “radioactive”. [14][15]
According to Palestine News Network, Dr. Al-Saqqa “confirmed that there were dozens of wounded legs and arms. Many of them had been burned from the inside, and distorted to the point that they cannot return to life again.”[16]
“When the shrapnel hit[s] the body, it causes very strong burns that destroy the tissues around the bones…it burns and destroys internal organs, like the liver, kidneys, and the spleen and other organs and makes saving the wounded almost impossible. As a surgeon, I have seen thousands of wounds during the Intifada, but nothing was like this weapon.”[17]
However, Dr. Al-Saqqa could not analyze the chemistry of the bizarre wounds. On the first day of the siege, June 27, Israel had conveniently destroyed Gaza’s only criminal laboratory. [18]
Despite his pleas to the “international community” to investigate and lend assistance in treating the victims, “no one has lifted a finger”, the doctor was quoted in mid-July. “What we found were journalists who came to take pictures, but as for the medical community, nothing.” [19]
On August 3, the United Nations Relief and Works Agency (UNRWA) reported that Commissioner-General Karen AbuZayd had visited Dr. Al-Saqqa’s hospital, “where the staff is struggling to deal with wounds resulting in an unusually high number of amputations.” Commissioner AbuZayd commented that “what we saw in Al-Shifa...was rather horrific.” [20]
According to Merlin (Medical Emergency Relief International), “75 per cent of war-wounded patients admitted at one hospital needed amputations” following an Israeli attack on Gaza City. [21]
The World Health Organization was reportedly considering an investigation into the injuries. Physicians for Human Rights - Israel “agreed to take away fragments of tissue from the bodies of Palestinians killed during the recent military operations in Gaza for possible analysis in Israel but urged the medics to seek an international investigation.” [22]
Tungsten in Tissue Samples: A DIME Weapon?
On October 19, Italy’s Rai24news televised an investigative report that supplied crucial new information. The Italian investigators had tissue samples from the victims in Gaza analyzed by Dr. Carmela Vaccaio at University Parma. Dr. Vaccaio reportedly found “a very high concentration of carbon and the presence of unusual materials, such as copper, aluminum and tungsten.” The doctor concluded that her "findings could be in line with the hypothesis that the weapon in question is DIME."
Rai24news reporters also talked to Maj. Gen. Yitzhak Ben-Israel, former chief of the IDF's weapons development program. General Ben-Israel appeared to be familiar with DIME weapons. He explained that, "one of the ideas is to allow those targeted to be hit without causing damage to bystanders or other persons." [23]
The US Air Force refers to this emerging realm of weaponry as FLM (Focused Lethality Munitions). FLM is expected to provide the ‘weapons of choice’ for targeting “terrorists hiding among civilians”, as a cheerleading Wall Street Journal article put it. [24]
With “focused lethality [and] higher energy materials...nano particles, intelligent fuzing, [and] mass focus lethality”, the Air Force “will be able to strike effectively, wherever and whenever necessary, with minimal collateral damage.” Ominously, the military thinks these weapons will allow it to target sites "previously off limits to the warfighter." [25][26]
This warfare of the future is reminiscent of what Israel has been doing for years, but with one-ton bombs, 155-mm artillery shells, and tank-fired antipersonnel flechette bombs. Are FLM weapons like DIME an improvement? Or will they actually increase civilian casualties and suffering, and mimic depleted uranium weapons by inducing disease and genetic damage in their victims? These disturbing questions will be explored in the next installment of this article.
:: Part 2 of 3 ::
“Horrific” wounds in Gaza may be warfare of the future
In early July, shortly after the beginning of Israel’s bloody military siege of the Gaza Strip, reports began to appear that Israeli forces were using a new weapon that inflicted strange and untreatable wounds, and significantly increased the death tolls of Israel’s attacks. [27][28]
Italian investigators have reported evidence that the unidentified Israeli weapon is probably Dense Inert Metal Explosives, or DIME, a so-called LCD (“low collateral damage”) weapon developed by the United States Air Force. [29]
DIME bombs blast a superheated “micro-shrapnel” of powdered heavy metal tungsten alloy (HMTA). Studies indicate that HMTA embedded in the body disrupts biochemistry and rapidly causes cancer. Like depleted uranium (DU), HMTA is genotoxic—it is capable of inflicting genetic mutations. [30-36]
Publicly slated for deployment in 2008, DIME bombs are small but unusually powerful. Their carbon fiber casings make “more of the blast energy…available as blast as opposed to being absorbed in [a] steel case". The carbon reportedly breaks into “thousands of harmless fibers” to prevent unintended casualties from casing shrapnel. [37]
The ‘footprint’ of the DIME blast is much smaller than a conventional bomb’s, because gravity and air resistance quickly drag the dense, finely powdered “micro-shrapnel” to the ground. The blast radius is reportedly as small as 25 feet. [38][39]
DIME is part of the Air Force’s Focused Lethality Munitions (FLM) program, which is expected to “allow” the targeting of “terrorists” wherever they are, even in places "previously off limits to the warfighter." [40]
The ideal of FLM is to reliably kill every human within the blast zone—one way or another. It is ‘total war’ on a 50-foot circle, within which deaths are not admitted as collateral, but purchased as insurance.
Israel’s new weapon “slices” off its victims’ legs, leaving “signs of heat and burns near the point of the amputation”. It’s “as if a saw was used to cut through the bone”, according to Dr. Habas al-Wahid, head of the ER at Gaza’s Shuhada al-Aqsa hospital. [41]
Viewing photographs of the living and dead Palestinian victims of this device, many of whom are children, we notice patches of darkened but unburned skin, possibly where metal powder was driven into and/or through the skin by blast force. A child's torso is peppered with holes, some of which, judging from doctors’ reports, probably tunnel through to exit wounds in the back. The skin and muscle of one victim is ripped into a blood-encrusted pulp, as if blasted at close range with tiny birdshot. Some of the corpses are unrecognizable. Most of the recent photos of “strange” wounds from Gaza appear to be consistent with what is known about DIME weapons. [42]
The area of a DIME blast should be treated with caution until it has been decontaminated (assuming this is possible). Depending on the local HMTA concentration, soil in the blast area may remain barren for an indefinite period of time, or it may grow plants internally contaminated with HMTA. [43][44]
The “who knew?” charade
In the scientific literature on tungsten and its alloys, the toxicity of HMTA stands apart. This formula (roughly 9 parts tungsten and one part nickel and cobalt or iron) damages DNA even when powders of the metals are simply mixed together. [30][31][35]
Implanting four tiny bits of weapons-grade HMTA in lab mice induced terminal cancer in 100 percent of the subjects. A powdered HMTA recipe was tumor-generating and capable of “genotoxic effects”. At least one experiment found parallels in the way DU and HMTA attack DNA. The results of another suggested that HMTA may pass its genetic damage down to the next generation. [34][31][35][36]
HMTA may be much more carcinogenic than DU when it is embedded in the body—as intended. “Tumors developed rapidly” in rats implanted with pellets of HMTA, but researchers “did not observe tumor formation in the DU-implanted rats.”
Multiple syndromes of heavy metal poisoning have also been attributed to this alloy, including polycythemia, which can be induced by cobalt overdose. Because HMTA contains far too little cobalt to cause the disease by itself, researchers suspected a synergistic effect among or between the metals. [34]
In a 2005 article reviewing the “status of health concerns” about depleted uranium and “surrogate metals” such as HMTA, three scientists at the Armed Forces Radiobiology Research Institute (AFRRI) wrote that “medical and political controversies surrounding the use of DU” had spurred “a search for substitute metals in armor-penetrating munitions.” [45]
“[N]ew alloys of tungsten/nickel/cobalt and tungsten/nickel/iron…rival DU in armor-penetrating performance”, and are “among the leading candidates to replace DU in selected munitions”. Some of this ordnance “has already been deployed, although on a relatively small scale.”
The article then reviews the science detailing the alarming health risks of HMTA, much of it conducted by the authors, whom we thank for their work. It then attempts to explain how the military’s favorite “surrogate metal” turned out to be almost as genotoxic as DU, and probably more carcinogenic:
“In many ways the development of substitutes for DU in munitions has followed a pattern similar to that for DU deployment, in that incomplete toxicological information was available prior to their release…it was assumed that many years of industrial use of tungsten and alloys such as tungsten carbide…meant they could be used as safely in armaments.”
We infer that it was reasonable for the military to deploy DU weapons, because the toxicological information was “incomplete”. It’s a strange scientific rigor that requires us to know exactly how a known poison works before we stop giving it to people.
The cold fact is that there never was a scientifically valid reason to “assume” that depleted uranium could be used “safely in armaments”. Quite the opposite; as we shall see in part three, the Army realized more than 60 years ago that finely powdered uranium products could make extremely potent antipersonnel weapons. [46]
We currently have “incomplete toxicological information” about HMTA, but for more than fifteen years we have had clear warnings about the health risks of combining these metals. US weapons scientists should have known as early as 1992 that mixing cobalt with tungsten could greatly increase the resulting alloy’s cancer potential. [47][48]
It is hardly news that nickel is carcinogenic and genotoxic, and specialists have long noted that heavy metal alloys tend to unpredictably amplify the toxicities of their component metals. With this kind of “incomplete” information at hand, could military scientists have reasonably “assumed” that nickel would be a “safe” addition to HMTA?
Concerns have been voiced about tungsten sport ammunition for several years. Tungsten alloy bullets, some also containing nickel and cobalt (for superior hardness), were found to pose potential environmental hazards in several studies. A probable link between industrial tungsten and leukemia has been identified. Compared to these findings, however, the toxicity of HMTA may be of a different order. [43][44]
The “who knew?” apologia offered by the AFRRI researchers asks us to assume that the scientists who developed DIME weapons proceeded in sheer ignorance of the existing science. They were so incompetent that they merely “assumed” that they could use any tungsten alloy.
Does this implausibility jibe with the rest of the picture? A multi-billion dollar military weapons program is stung by the “controversies” surrounding its toxic DU-uranium weapons, and is under pressure to produce an expedient alternative. Would this program’s scientists have been allowed to be so cavalier about consulting the literature? Would the replacement metal be chosen on blind faith, without bothering to conduct even simple studies of its potential health impacts?
Logically, we must conclude that the military developed HMTA in the knowledge that it could have significant carcinogenic and genotoxic effects. Did they “assume” that saying “tungsten is safer than DU” would take care of the matter?
Perhaps relatively non-toxic tungsten carbide, famed for its hardness and cutting ability, would not have sufficed for the purposes of the DIME bomb. Focused Lethality Munitions like DIME must kill all of their victims. Slicing off their arms and legs is not enough.
The last installment of this article will trace the roots of HMTA in depleted uranium and decades of US warfare with poisonous, DNA-damaging powders. Then we will return to Gaza to consider the damage done, and the damage to come, if the warmakers have their way.
:: Part 3 of 3 ::
The human genome: target or innocent bystander?
Since early July, Israeli forces have been using a new weapon in the Gaza Strip that inflicts strange and deadly wounds. Doctors and medics say the unidentified device has significantly increased fatalities from Israel’s attacks. [49][50]
In the first two parts of this article we reviewed evidence that Israel’s new weapon may be Dense Inert Metal Explosives (DIME), a “low collateral damage” weapon developed by the US Air Force. The DIME bomb’s “micro-shrapnel” is reportedly made of HMTA, a tungsten alloy that disrupts body biochemistry, damages the immune system, rapidly causes cancer, and attacks DNA (genotoxic). [51-56]
The Road to DIME
DIME weapons are "spin-offs" from the military’s “bunker buster” research. Initially, “bunker busters” were made with depleted uranium (DU), which had already been used in armor-piercing bombs, bullets, and artillery shells. [57]
The former director of the US Army’s Depleted Uranium project, Dr. Douglas Rokke, warns us that DU is an “illegal…radioactive toxic material”, the use of which “is absolutely unacceptable, and a crime against humanity.” [58]
During Gulf War I, US forces deployed more than 300 tons of DU in Iraq. A few years later, more was dropped during Operation Desert Fox. Iraqi doctors reported alarming rises in the incidence of cancer, leukemia, and birth defects, in clusters closely correlated with US bombsites. Scientists found strong links between DU and Gulf War Syndrome, which is slowly killing thousands of veterans. [59-61]
Despite the science, the vets, and the tragedies in Iraq, the US has stubbornly refused to end its use of DU. US-UK forces may have expended more than 2000 additional tons of DU in Iraq since March 2003. Nowadays, however, commanders are supposed to warn GIs to avoid contact with the results of their work. [62]
After the 2001-2002 bombing of Afghanistan, the Uranium Medical Research Centre (UMRC) found that the urine of Afghanis living near US bombing sites contained 4 to 20 times the normal level of non-depleted uranium (NDU). These unexpected results could not “be explained by…any known geological or other features in the area.”
UMRC researchers were “shocked” that, “without exception, at every bombsite investigated, people are ill…[with] symptoms consistent with internal contamination by uranium.” [63]
Their field results indicated that our weapons scientists had “progressed” beyond DU to NDU, a processed form of pure uranium that is even more toxic than the depleted form. The “slightly enriched” uranium reported from recent Israeli bombsites in Lebanon may possibly be NDU from modified GBU 28 ‘bunker busters’ supplied by the United States. [64][65]
Dual-Purpose Munitions
Considering the scope of their destructive power, DU and NDU may be said to function as Dual-Purpose Munitions, like cluster bomblets that kill both tanks and people. As their exotic metallurgy “burns” through concrete and steel, DU and NDU bombs are converted to micron-sized particles that sicken and kill and murder the next generation in the womb. [66][67]
Agent Orange, an herbicide heavily used during the war on Vietnam, also performed two functions. It obliterated the ‘jungle cover hiding the Viet Cong’ while it ‘weakened the enemy’ with burns, illness, and death, and corrupted the DNA of hundreds of thousands of Vietnamese. The third generation of its disfigured and suffering victims is now being born. [68][69]
This madness seems to have begun during World War II, within the Manhattan Project that built the first atomic bomb. In a 1943 memo to Brigadier General L. R. Groves, three researchers proposed steps to develop:
“a gas warfare instrument” [of radioactive material, such as uranium] “ground into particles of microscopic size to form dust and smoke….in this form it would be inhaled by personnel. The amount necessary to cause death to a person inhaling the material is extremely small. It has been estimated that one millionth of a gram accumulating in a person's body would be fatal. There are no known methods of treatment for such a casualty.” [70]
The good doctors were concerned the Germans might be preparing such a weapon. They urged the Army to be ready to respond, or act, in kind. General Groves promptly followed their recommendations.
The toxic HMTA “micro-shrapnel” spewed by DIME weapons appears to be the latest development in a long string of carcinogenic and genotoxic weapons developed and deployed by the US military.
Return to Gaza: The mythology of murder
Israel has denied using DIME weapons. Nonetheless, Israel’s military has used the occupied Palestinian territories as a weapons development zone for decades, testing bright ideas like depleted uranium and poison gases. It would not surprise us to find that it is now testing a weapon for the US Air Force on Palestinians in Gaza. [71]
Unfortunately, the DIME hypothesis is the most plausible explanation for the grotesque effects of Israel’s new weapon. We can only pray that we have not witnessed the first experiment in the effects of embedded HMTA in human subjects.
Still, DIME may not explain all of the evidence. For example, one of the metals found in victims’ wounds was copper. DIME bombs are not known to contain significant copper, but another US marvel, the Sensor Fuzed Weapon (SFW), sprays slugs of molten copper at its targets. Is Israel also testing the SFW? [72][73]
If DIME weapons are designed to reduce civilian casualties, why has Israel’s ‘mystery weapon’ increased the civilian death toll? Perhaps this question should be addressed to the advocates of Focused Lethality Munitions, and to the remote-control operators of Israel’s drone aircraft and their commanders and politicians.
Although much remains unclear about Israel’s new weapon, a few devastating facts are indisputable:
The weapon causes enormous and indiscriminate pain and suffering.
It operates as both a chemical weapon and an anti-personnel explosive. At the very least, it is likely to induce heavy metal poisoning in its surviving victims.
The weapon has significantly increased civilian mortality rates, in part because it inflicts virtually untreatable wounds.
Despite this public parade of horrors, Israeli forces have continued to use this weapon against Palestinians in the Gaza Strip for nearly five months.
“Whenever and wherever necessary”
If the DIME hypothesis is confirmed, authorities will probably explain that it is a new class of weapon not regulated by international law. The truth is that existing conventions and treaties have already prohibited some of the most egregious effects of the new weapon.
To cite one example, the bomb may be in direct violation of Protocol I of the 'Geneva Convention on Certain Conventional Weapons', which "prohibits the use of any weapon the primary effect of which is to injure by fragments which in the human body escape detection by X-rays." [74]
We will likely be told that DIME weapons provide a more “humane” way to fight “terrorism” by “reducing collateral damage” and “helping US troops win hearts and minds”. At the same time, we’ll be assured that the new weapon “packs quite a punch” and will “give our troops more options” to “take the battle to the enemy”, even if he is “hiding among civilians”.
Whether Israel’s new weapon is the Air Force’s DIME bomb or another similarly dreadful invention, the horrors unfolding in Gaza make it clear that “Focused Lethality” is a blood-drenched lie. It promises only a deadlier form of indiscriminate warfare.
US plans to explode payloads of cancer-causing genotoxic heavy metal powder “wherever and whenever necessary” may portend an escalation of a campaign currently limited to the vicinity of “hard targets” we attack with DU and NDU. Whatever we make of the intent behind these weapons, the habitual result is chemical-genetic warfare. It cannot be allowed to continue.
Notes:
[1]. Palestinian injuries suggest Israel is using chemical weapons in Gaza
Ma'an News, 7/10/2006
http://www.maannews.net/en/index.php? opr=ShowDetails&ID=13044
[2]. Israel used chemical weapons in Lebanon and Gaza
By Jean Shaoul, Centre for Research on Globalization/wsws.org, 10/24/2006
http://wsws.org/articles/2006/oct2006/
isra-o24.shtml
[3]. Italian TV: Israel used new weapon prototype in Gaza Strip
Ha'aretz, 10/19/2006
http://www.haaretz.com/hasen/pages/
ShArt.jhtml?itemNo=772894
[4]. Dense Inert Metal Explosive (DIME)
GlobalSecurity.org, 10/18/2006
http://www.globalsecurity.org/military/
systems/munitions/dime.htm
[5]. Abstract: Potential late health effects of depleted uranium and tungsten used in armor-piercing munitions: comparison of neoplastic transformation and genotoxicity with the known carcinogen nickel
Miller, AC, et al, PubMed, 11/26/2006
http://www.ncbi.nlm.nih.gov/entrez/
query.fcgi?cmd=Retrieve&db=PubMed&
list_uids=11873492&dopt=Abstract
[6]. Neoplastic transformation of human osteoblast cells to the tumorigenic phenotype by heavy metal–tungsten alloy particles: induction of genotoxic effects
Miller, AC, et al
Carcinogenesis, Vol. 22, No. 1, 115-125, January 2001, Oxford University Press
http://carcin.oxfordjournals.org/cgi/content/
full/22/1/115
[7]. Abstract: Carcinogenic Potential of Depleted Uranium and Tungsten Alloys
Alexandra C Miller, Ph. D., Department Of Defense, Armed Forces Radiobiology Research Institute (AFRRI)
http://www.deploymentlink.osd.mil/
du_library/reports/projects/dod122.htm
[8]. Depleted uranium-catalyzed oxidative DNA damage: absence of significant
alpha particle decay
Miller, AC, et al, Journal of Inorganic Biochemistry, Issue 91, 2002 pp. 246– 252
http://www.afrri.usuhs.mil/www/outreach/
pdf/tungsten_cancer.pdf
[9]. Embedded Weapons-Grade Tungsten Alloy Shrapnel Rapidly Induces Metastatic High-Grade Rhabdomyosarcomas in F344 Rats
Kalinich et al, Environmental Health Perspectives Volume 113, Number 6, June 2005
http://www.ehponline.org/members/2005/
7791/7791.html
[10]. Abstract: Effect of the militarily-relevant heavy metals, depleted uranium and heavy metal tungsten-alloy on gene expression in human liver carcinoma cells (HepG2)
By Miller, AC, et al, SpringerLink/Molecular and Cellular Biochemistry, 1/1/2004
http://www.springerlink.com/content/u8830 115617471jl/
[11]. Preconceptional paternal exposure to radiation or heavy metals like cadmium can induce cancer in unexposed offspring
By Alexandra C. Miller, Rafael Rivas, Robert J. Merlot and Paul, Carcinogenesis 5: Environmental and Endogenous Carcinogens/Proc Amer Assoc Cancer Res, Volume 47, 2006
http://www.aacrmeetingabstracts.org/cgi/
content/abstract/2006/1/448-b
[12]. If Americans Knew
http://www.ifamericansknew.org/
[13]. Israel 'is using chemical ammunition' in Gaza
By Duraid Al Baik, Centre for Research on Globalization/Gulf News, 6/13/2006
http://www.globalresearch.ca/index.php? context=viewArticle&code=
AL%2020060713&articleId=2730
[14]. Are New Weapons Being Used In Gaza and Lebanon
By David Halpin MB BS FRCS, Electronic Intifada, 8/14/2006
http://electronicintifada.net/v2/article5528.
shtml
[15]. Ministry of Health report on toxic Israeli weapons confirmed by Gaza City medical sources
Palestine News Network, 7/13/2006
http://www.pnn.ps/english/archive2006/
jul/week2/130706/report5.htm
[16]. ibid.
[17]. Doctors Report Unusual Weapon Used in Gaza
Pacifica/Free Speech Radio News 7/11/2006
http://www.pacifica.org/programs/fsrn/
fsrn_060711.html
[18]. Israel 'is using chemical ammunition' in Gaza
Centre for Research on Globalization/Gulf News, 6/13/2006
http://www.globalresearch.ca/index.php? context=viewArticle&code=
AL%2020060713&articleId=2730
[19]. Ministry of Health report on toxic Israeli weapons confirmed by Gaza City medical sources
Palestine News Network, 7/13/2006
http://www.pnn.ps/english/archive2006/
jul/week2/130706/report5.htm
[20]. UNRWA Commissioner-General Karen AbuZayd: "Please don't forget what's going on in Gaza"
ReliefWeb/UNRWA, 8/3/2006
http://www.reliefweb.int/rw/RWB.NSF/
db900SID/EVOD-6SBJDR? OpenDocument&rc=3&emid=ACOS-635PFR
[21]. Hospitals in Gaza overwhelmed and running out of supplies
Electronic Intifada/Merlin, 8/8/2006
http://electronicintifada.net/v2/article5455.
shtml
[22]. Gaza doctors encounter 'unexplained injuries'
Donald Macintyre, The Independent 9/4/2006
http://news.independent.co.uk/world/
middle_east/article1359830.ece
[23]. Italian TV: Israel used new weapon prototype in Gaza Strip
Ha'aretz, 10/12/2006
http://www.haaretz.com/hasen/pages/ShArt.jhtml?itemNo=772894
[24]. Air Force seeks a bomb with less bang
By Greg Jaffe, The Wall Street Journal/Pittsburgh Post-Gazette, 4/11/2006
http://www.post-gazette.com/pg/06096/679996-84.stm
[25]. Munition Technology Drivers
By Col. Thomas “Mas” Masiell, Air Force Research Laboratory, 12/1/2006
http://www.dtic.mil/ndia/2001munitions/masiello.pdf
[26]. USAF Unfunded Priority List (UPL)
SAF/FMB POC, FY 2007, February 2006, Page 54
http://wwwd.house.gov/hasc_democrats/
Issues%20109th/unfunded/AF%20UFR%
20FY07.pdf
[27]. Israel accused of using 'Dime' bombs
AlJazeera, 10/13/2006
http://english.aljazeera.net/NR/exeres/
B79DF070-B20C-47A7-A204-
08297E5FC1B2.htm
[28]. Israel used chemical weapons in Lebanon and Gaza
By Jean Shaoul, Centre for Research on Globalization/wsws.org, 10/24/2006
http://wsws.org/articles/2006/oct2006/isra-o24.shtml
[29]. Italian TV: Israel used new weapon prototype in Gaza Strip
Ha'aretz, 10/19/2006
http://www.haaretz.com/hasen/pages/
ShArt.jhtml?itemNo=772894
[30]. Abstract: Potential late health effects of depleted uranium and tungsten used in armor-piercing munitions: comparison of neoplastic transformation and genotoxicity with the known carcinogen nickel
Miller, AC, et al, PubMed, 11/26/2006
http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=PubMed&list_uids
=11873492&dopt=Abstract
[31]. Neoplastic transformation of human osteoblast cells to the tumorigenic phenotype by heavy metal–tungsten alloy particles: induction of genotoxic effects
Miller, AC, et al
Carcinogenesis, Vol. 22, No. 1, 115-125, January 2001, Oxford University Press
http://carcin.oxfordjournals.org/cgi/content/
full/22/1/115
[32]. Abstract: Carcinogenic Potential of Depleted Uranium and Tungsten Alloys
Alexandra C Miller, Ph. D., Department Of Defense, Armed Forces Radiobiology Research Institute (AFRRI)
http://www.deploymentlink.osd.mil/du_
library/reports/projects/dod122.htm
[33]. Depleted uranium-catalyzed oxidative DNA damage: absence of significant
alpha particle decay
Miller, AC, et al, Journal of Inorganic Biochemistry, Issue 91, 2002 pp. 246– 252
http://www.afrri.usuhs.mil/www/outreach/
pdf/tungsten_cancer.pdf
[34]. Embedded Weapons-Grade Tungsten Alloy Shrapnel Rapidly Induces Metastatic High-Grade Rhabdomyosarcomas in F344 Rats
Kalinich et al, Environmental Health Perspectives Volume 113, Number 6, June 2005
http://www.ehponline.org/members/2005/
7791/7791.html
[35]. Abstract: Effect of the militarily-relevant heavy metals, depleted uranium and heavy metal tungsten-alloy on gene expression in human liver carcinoma cells (HepG2)
By Miller, AC, et al, SpringerLink/Molecular and Cellular Biochemistry, 1/1/2004
http://www.springerlink.com/content/
u8830115617471jl/
[36]. Preconceptional paternal exposure to radiation or heavy metals like cadmium can induce cancer in unexposed offspring
By Alexandra C. Miller, Rafael Rivas, Robert J. Merlot and Paul, Carcinogenesis 5: Environmental and Endogenous Carcinogens/Proc Amer Assoc Cancer Res, Volume 47, 2006
http://www.aacrmeetingabstracts.org/cgi/
content/abstract/2006/1/448-b
[37]. Air Force seeks a bomb with less bang
By Greg Jaffe, The Wall Street Journal/Pittsburgh Post-Gazette, 4/11/2006
http://www.post-gazette.com/pg/06096/679996-84.stm
[38]. Cancer Worries for New U.S. Bombs
DefenseTech.org, 5/20/2006
http://www.defensetech.org/archives/
002434.html
[39]. Dense Inert Metal Explosive (DIME)
GlobalSecurity.org, 10/18/2006
http://www.globalsecurity.org/military/
systems/munitions/dime.htm
[40]. USAF Unfunded Priority List (UPL)
SAF/FMB POC, FY 2007, February 2006, Page 54
http://wwwd.house.gov/hasc_democrats/
Issues%20109th/unfunded/AF%20UFR%
20FY07.pdf
[41]. Italian TV: Israel used new weapon prototype in Gaza Strip
Ha'aretz, 10/19/2006
http://www.haaretz.com/hasen/pages/
ShArt.jhtml?itemNo=772894
[42]. Effects of Israel's New Weapon
Vermonters for a Just Peace in Palestine/Israel
http://www.vtjp.org/report/neweapon
images.htm
[43]. Possible Health And Environmental Impacts Of Tungsten In Lead Replacement Shot
Paul Harrison and Karen Bradley, MRC Institute for Environment and Health 2005
http://www.defra.gov.uk/ENVIRONMENT/
chemicals/achs/050906/achs0516a.pdf
[44]. Tungsten Effects on Soil Environments
Nikolay Strigul, et al, UMass, Annual International Conference on Soil, Sediments and Water, 10/18/2004
http://www.umasssoils.com/abstracts2004/
Tuesday/trainingranges.htm#Tungsten%
20Effects%20on%20Soil%20Environments
[45]. Status of Health Concerns about Military Use of Depleted Uranium and Surrogate Metals in Armor-Penetrating Munitions
D.E. McClain, A.C. Miller, and J.F. Kalinich, NATO, 2005
http://www.afrri.usuhs.mil/www/outreach/
pdf/mcclain_NATO_2005.pdf
[46]. Memorandum to: Brigadier General L. R. Groves From: Drs. Conant, Compton, and Urey
Midfully.org/War Department, United States Engineer Office, Manhattan District, Oak Ridge Tennessee, 10/30/1943
http://www.mindfully.org/Nucs/Groves-
Memo-Manhattan30oct43.htm
[47]. Abstract: Comparative study of the acute lung toxicity of pure cobalt powder and cobalt-tungsten carbide mixture in rat
Lasfargues G., et al, Toxicology and Applied
Pharmacology, 1992
http://cat.inist.fr/?aModele=afficheN&cpsidt
=5201679
[48]. Evaluation of the role of reactive oxygen species in the interactive toxicity of carbide-cobalt mixtures on macrophages in culture
D. Lison and R. Lauwerys, SpringerLink//Archives of Toxicology, 6/1/1993
http://www.springerlink.com/content/
k2u94u07558q6224/
[49]. Gaza doctors say patients suffering mystery injuries after Israeli attacks
By Rory McCarthy, The Guardian, 10/18/2006
http://www.guardian.co.uk/israel/Story/
0,,1924675,00.html
[50]. Israel used chemical weapons in Lebanon and Gaza
By Jean Shaoul, Centre for Research on Globalization/wsws.org, 10/24/2006
http://wsws.org/articles/2006/oct2006/
isra-o24.shtml
[51]. Abstract: Potential late health effects of depleted uranium and tungsten used in armor-piercing munitions: comparison of neoplastic transformation and genotoxicity with the known carcinogen nickel
Miller, AC, et al, PubMed, 11/26/2006
http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=PubMed&list_
uids=11873492&dopt=Abstract
[52]. Neoplastic transformation of human osteoblast cells to the tumorigenic phenotype by heavy metal–tungsten alloy particles: induction of genotoxic effects
Miller, AC, et al
Carcinogenesis, Vol. 22, No. 1, 115-125, January 2001, Oxford University Press
http://carcin.oxfordjournals.org/cgi/content/
full/22/1/115
[53]. Abstract: Carcinogenic Potential of Depleted Uranium and Tungsten Alloys
Alexandra C Miller, Ph. D., Department Of Defense, Armed Forces Radiobiology Research Institute (AFRRI)
http://www.deploymentlink.osd.mil/du_
library/reports/projects/dod122.htm
[54]. Depleted uranium-catalyzed oxidative DNA damage: absence of significant
alpha particle decay
Miller, AC, et al, Journal of Inorganic Biochemistry, Issue 91, 2002 pp. 246– 252
http://www.afrri.usuhs.mil/www/outreach/
pdf/tungsten_cancer.pdf
[55]. Embedded Weapons-Grade Tungsten Alloy Shrapnel Rapidly Induces Metastatic High-Grade Rhabdomyosarcomas in F344 Rats
Kalinich et al, Environmental Health Perspectives Volume 113, Number 6, June 2005
http://www.ehponline.org/members/2005/
7791/7791.html
[56]. Abstract: Effect of the militarily-relevant heavy metals, depleted uranium and heavy metal tungsten-alloy on gene expression in human liver carcinoma cells (HepG2)
By Miller, AC, et al, SpringerLink/Molecular and Cellular Biochemistry, 1/1/2004
http://www.springerlink.com/content/
u8830115617471jl/
[57]. Preconceptional paternal exposure to radiation or heavy metals like cadmium can induce cancer in unexposed offspring
By Alexandra C. Miller, Rafael Rivas, Robert J. Merlot and Paul, Carcinogenesis 5: Environmental and Endogenous Carcinogens/Proc Amer Assoc Cancer Res, Volume 47, 2006
http://www.aacrmeetingabstracts.org/cgi/
content/abstract/2006/1/448-b
[58]. Cancer Worries for New U.S. Bombs
DefenseTech.org, 5/20/2006
http://www.defensetech.org/archives/
002434.html
[59]. Depleted Uranium and US-Israeli Bombs
By Dr. Doug Rokke, PhD, Media Lens, 7/24/2006
http://members5.boardhost.com/medialens/
msg/1153759483.html
[60]. Dirty Weapons - Casualties From Iraq War Will Mount
By Chalmers Johnson, Pacific News Service, 5/3/2003
http://news.pacificnews.org/news/view
_article.html?article_id=84a8df02a7c1f37
0c5ca152d5ef14d6b
[61]. Uranium Radiation Levels in Afghanistan Not Attributable to Depleted Uranium
Centre for Research on Globalization - Middle East, 6/5/2003
http://www.globalresearch.ca/articles/
UMR306B.html
[62]. Depleted Uranium Radioactive Contamination In Iraq: An Overview
By Prof Souad N. Al-Azzawi, Centre for Research on Globalization - Middle East, 8/31/2006
http://www.globalresearch.ca/index.php?
context=viewArticle&code=
AL-20060831&articleId=3116
[63]. Use of Depleted Uranium Weapons Lingers as Health Concern
By Larry Johnson, Common Dreams, 8/4/2003
http://www.commondreams.org/headlines
03/0804-04.htm
[64]. Further Evidence Of Enriched Uranium In The Air In Lebanon Following The Recent Conflict
Stop Uranium Wars/Pandora DU research Project, 11/22/2006
http://www.stopuraniumwars.blogspot.com/
[65]. Mystery of Israel's secret uranium bomb
By Robert Fisk, The Independent, 10/28/2006
http://news.independent.co.uk/world/fisk/
article1935945.ece
[66]. The Real Dirty Bombs: Depleted Uranium
By Christopher Bollyn, Nuclear Age Peace Foundation, 8/6/2004
http://www.wagingpeace.org/articles/2004/
08/06_bollyn_real-dirty-bombs.htm
[67]. Depleted Uranium
Australian Peace Committee, 12/2/2006
http://www.peacecourier.com/depleted_
uranium.htm
[68]. Vietnam Agent Orange Relief & Responsibility Campaign
http://www.vn-agentorange.org/
[69]. Agent Orange DNA injury confirmed in Vietnam veterans
By Patrick Gower, New Zealand Herald, 7/29/2006
http://subs.nzherald.co.nz/feature/story.
cfm?c_id=500855&objectid=10393538
[70]. Memorandum to: Brigadier General L. R. Groves From: Drs. Conant, Compton, and Urey
Midfully.org/War Department, United States Engineer Office, Manhattan District, Oak Ridge Tennessee, 10/30/1943
http://www.mindfully.org/Nucs/
Groves-Memo-Manhattan30oct43.htm
[71]. The Israeli Poison Gas Attacks
James Brooks, Vermonters for a Just Peace in Palestine/Israel
http://www.vtjp.org/report/
[72]. CBU-97
Wikipedia
http://en.wikipedia.org/wiki/CBU-97
[73]. Textron Systems' Sensor Fuzed Weapon Production to Include Maritime Capability
Textron Systems Corporation, 8/10/2006
http://www.systems.textron.com/mainframe /pressroom/archives/2006/08_10_06.html
[74]. Convention on Prohibitions or Restrictions on the Use of Certain Conventional Weapons...
United Nations: International Law, 10/10/1980
http://www.un.org/millennium/law/xxvi-
18-19.htm