Biowarfare Research: Lifting the Lid on America

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Biowarfare Research: Lifting the Lid on America

Postby American Dream » Sun Jul 26, 2009 5:35 pm

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Biowarfare Research: Lifting the Lid on America's "28 Days Later"


The dystopian British sci-fi film 28 Days Later opens with animal rights activists breaking into the Cambridge Primate Research facility to free chimpanzees used in a secret weapons program.

Terrified by the intrusion, a scientist warns the raiders that the chimps are infected with a genetically-modified pathogen. Ignoring his admonition, the chimps are let loose from their cages and immediately attack everyone in sight, unleashing a plague of unimaginable proportions.

Despite the film's fanciful scenario (with animal rights' campaigners clearly focused in the cross-hairs) this grim, cautionary tale does contain a kernel of truth. While marauding gangs of flesh-eating zombies haven't invaded our cities, a subtler threat looms on the horizon.

The sixth anniversary of the murder of British bioweapons expert Dr. David Kelly on July 17, 2003, lifted the lid on more than government lies that smoothed the way for the illegal invasion and occupation of Iraq; it exposed the shadowy world of germ warfare research in Britain and the United States.

Along with the 2001 anthrax attacks in America that murdered five people and exposed some 10,000 others to a weaponized form of the bacteria, Kelly's death under highly questionable circumstances focused attention on the West's bioweapons establishment. For a fleeting instant, all eyes were trained on an international network of medical researchers, corporate grifters and Pentagon weaponeers busy as proverbial bees experimenting with deadly microorganisms.

And then as they say, things went dark; as more bodies piled up, cases were "closed" and the money kept on flowing...

An Expansive Bioweapons-Industrial Complex

The production of biological weapons were ostensibly banned when the United States signed the Biological Weapons Convention (BWC) in 1975. However, the absence of any formal verification regime limited, some would argue purposely so, the effectiveness of the treaty from the get-go.

Indeed, a giant loop hole in the BWC allows for the production of "small quantities" of pestilential agents "for medical and defensive purposes." Note however, it is is not the production of said agents that are prohibited as such but rather, their transformation into "weapons, equipment or means of delivery ... for hostile purposes or in armed conflict."

And with the September 11 and anthrax attacks as a pretext, the United States embarked on a systematic and reckless program to expand research into the creation of prohibited weapons systems. Along with renewed interest in these dodgy projects, now euphemistically dubbed "biodefense" to avoid breaching the BWC, came a huge increase in funding as new facilities are built and older ones "upgraded." A May 2009 report by the Congressional Research Service (CRS) estimates that overall government spending has "increased from $690 million in FY2001 to $5.4 billion in FY2008."

According to the Washington D.C.-based Center for Arms Control and Non-Proliferation since the 2001 terrorist attacks "the U.S. government has spent or allocated nearly $50 billion among 11 federal departments and agencies to address the threat of biological weapons. For Fiscal Year 2009 (FY2009), the Bush Administration proposes an additional $8.97 billion in bioweapons-related spending, approximately $2.5 billion (39%) more than the amount that Congress appropriated for FY2008."

The bulk of these funds according to the Center have gone to the Department of Health and Human Services' Biomedical Advanced Research and Development Authority, or BARDA ($31.5 billion), the Defense Department ($11.8 billion), Department of Homeland Security ($3.3 billion) and Project BioShield ($5.5 billion).

Yet according to numerous studies, deadly pathogens are far more likely to spread like wildfire as the result of a laboratory accident than an attack by germ-wielding terrorists. As I write, labs with Biosafety Level 3 (BSL-3) and Biosafety Level 4 (BSL-4) facilities are sprouting up like poisonous mushrooms across the United States.

A BSL-3 lab designation means that a facility is equipped to handle indigenous or exotic agents that may cause serious or potentially lethal disease after inhalation. Examples of substances handled by a BSL-3 lab include tuberculosis, anthrax, West Nile virus, SARS, salmonella, and yellow fever.

On the other hand, a BSL-4 lab handles the most deadly pathogens known to humankind; in other words, aerosol-transmitted infectious agents that cause fatal diseases for which no known treatments are available. Examples of substances handled by a BSL-4 lab include: Marburg virus, Ebola virus, Lassa fever and Crimean-Congo hemorrhagic fever.

CRS researchers reported that "Non-federal entities have also expanded or constructed additional high-containment laboratories. In addition to the threat of bioterrorism, an increasing awareness of the threat posed by emerging and re-emerging diseases has led to the proliferation of high-containment laboratories internationally, as the technologies used are widely available."

Shockingly, CRS was unable to determine the exact number of BSL-3 laboratories currently operating in America. However Congress' research arm said that "the total amount of planned or existent BSL-4 space in the United States has increased by an estimated twelve-fold since 2004."

Much of this work, conveniently, is being contracted out to private corporations with little or no effective oversight. Among the more prominent firms to have received the federal government's largesse for BSL-3 and BSL-4 work according to CRS, one finds the "Lovelace Respiratory Research Institute, Battelle Memorial Institute, Southern Research Institute, and others." Indeed, much can be hidden here, including outsourced secret weapons research, under the rubric of "proprietary information" and "intellectual property" of course!

During 2007 hearings before Congress' Committee on Energy and Commerce's Subcommittee on Oversight and Investigations, committee Chairman Rep. Bart Stupak (D-MI) said:

These BSL–3 and 4 labs are the facilities where research is conducted on highly infectious viruses and bacteria that can cause injury or death. Some of the world's most exotic and most dangerous diseases are handled at BSL–3 and 4 labs, including anthrax, foot-and-mouth disease and Ebola fever. The accidental or deliberate release of some of the biological agents handled at these labs could have catastrophic consequences. Yet, as we will hear from the Government Accountability Office, GAO, no single Government agency has the ultimate responsibility for ensuring the safety and securing of these high-containment labs. However, GAO states there is a major expansion of the number of BSL laboratories is occurring both in United States and abroad but the full extent of that expansion is unknown. ("Germs, Viruses and Secrets: The Silent Proliferation of Bio-Laboratories in the United States," Hearing Before the Subcommittee on Oversight and Investigations of the Committee on Energy and Commerce, U.S. House of Representatives, October 4, 2007, Serial No. 110-70, pp. 1-2)

The hearings revealed that no one "in the Federal Government even knows for sure how many of these labs there are in the United States, much less what research they are doing or whether they are safe and secure." Neither "safe" nor "secure" such facilities however, are highly profitable.

During 2007 alone, some 100 "incidents" were reported; however, "there are indications that the actual number of incidents may be much higher," according to Rep. Stupak. Reporting guidelines are so lax that dangerous pathogens such as hantavirus, SARS and dengue fever "are not on the select agent list" nor are there requirements "that the theft, loss or release of these agents ... be reported to Federal officials."

According to Edward Hammond, director of the now-defunct Sunshine Project, some 20,000 people working at more than 400 sites in the U.S. conduct research on organisms that can be used as bioweapons. This represents a tenfold increase in employment at such facilities since the 2001 anthrax attacks.

Using the Freedom of Information Act to pry data from the federal government, Hammond obtained records from a score of university biosafety committees. What he discovered was disturbing to say the least. Plague, anthrax, Rocky Mountain spotted fever, tularemia, brucellosis and Q fever; these are some of the deadly pathogens that escaped containment through poor safety practices and resulted in the inadvertent sickening of lab workers.

Scientists have warned for years that the more people who handle these toxic substances, the higher the probability that mishaps will occur. Among the more well-publicized incidents, Hammond reported the following:

* Texas A&M University: workers were exposed to Q fever when it escaped containment;
* University of New Mexico: one worker was jabbed with an anthrax-laden needle while another was stuck with a syringe filled with an undisclosed, genetically altered microbe;
* University of Ohio Medical Center: workers are exposed to and infected with Valley Fever;
* University of Chicago: a syringe puncture of a lab worker with an undisclosed substance that required heavy containment, most likely anthrax or plague;
* University of California at Berkeley: workers handled the air-borne toxin Rocky Mountain Spotted Fever without containment. It had been mislabeled as "harmless".


More recently, Global Security Newswire reported in June that an inventory at the U.S. Army Medical Research Institute of Infectious Diseases (USAMRIID) at Fort Detrick, Md., "found nearly 10,000 more vials of potentially lethal pathogens than were known to be stored at the site."

Claiming that there are "multiple layers of security," Ft. Detrick's deputy commander Col. Mark Kortepeter said it was "extremely unlikely" that any of the center's samples had been smuggled out. "Unlikely," but not impossible.

Amongst the 9,200 extra samples uncovered during the inventory were "bacterial agents that cause plague, anthrax and tularemia; Venezuelan, Eastern and Western equine encephalitis viruses; Rift valley fever virus; Junin virus; Ebola virus; and botulinum neurotoxins." So much for a "culture of safety"!

Any one of these pathogens should they escape or made to "disappear," could be transformed into a doomsday weapon.

Designer Genes, Designer Weapons

In Emerging Technologies: Genetic Engineering and Biological Weapons, researcher Edward Hammond described how "Genetic engineering can contribute to offensive BW programs in a variety of ways. With genetic manipulation, classical biowarfare agents such as anthrax or plague may be made more efficient weapons. Barriers to access to agents such as smallpox, Ebola or the Spanish flu are being lowered by genetic and genomic techniques."

No longer the province of science fiction, recombinant DNA research is being exploited by enterprising corporate grifters for decidedly sinister purposes. Hammond writes that while "access to highly virulent agents and strains is increasingly regulated and restricted," with lethal toxins such as the smallpox virus "eradicated outside the laboratory more than 20 years ago ... it is only a question of time before the artificial synthesis of agents or agent combinations becomes possible."

The available evidence suggests such work, alarmingly, is advancing at a rapid rate.

In 2002, poliovirus was synthesized by a research team at the University of New York in Stony Brook. Hammond writes that "researchers built poliovirus 'from scratch' through chemical synthesis. Starting with the gene sequence of the agent, which is available online, the researchers synthesized virus sequences in the lab and ordered other tailor-made DNA sequences from a commercial source. They then combined them to form the full polio genome. In a last step, the DNA-sequence was brought to life by adding a chemical cocktail that initiated the production of a living, pathogenic virus. The experiment was funded by the US Defense Advanced Research Projects Agency (DARPA)."

While poliovirus is not "well suited" as a bioweapon, "the experiment exemplifies possibilities that generate real problems if similar techniques become applicable to agents such as smallpox." Hammond averred that in 2002 "such a technique was demonstrated." Indeed, "the full sequences of at least two different smallpox strains are available in the internet, and most recently a new internet site dedicated to poxvirus genomic sequences has been launched."

As frightening as the potential for genetically engineering smallpox as a bioweapon, U.S. researchers, led by a Pentagon pathologist "recently began to genetically reconstruct" the dangerous influenza strain responsible for the 1918-1919 pandemic. "In one experiment" Hammond informs us, "a partially reconstructed 1918 virus killed mice, while virus constructs with genes from a contemporary flu virus had hardly any effect." During the 1918-1919 outbreak some 40 million people died in the global pandemic.

Hammond reports that a sample of lung tissue from a 21-year-old soldier who died in 1918 at Ft. Jackson in South Carolina "yielded what the Army researchers were looking for: intact pieces of viral RNA that could be analysed and sequenced. In a first publication in 1997, nine short fragments of Spanish flu viral RNA were revealed. Due to the rough tissue preparation procedure in 1918, no living virus or complete viral RNA sequences were recovered."

But far from inhibiting Pentagon researchers, biowarfare proponents were jumping for joy when Army scientists recovered intact pieces of viral RNA that were then subsequently pulled apart and analyzed. By 2002 according to Hammond, "four of the eight viral RNA segments had been completely sequenced, including the two segments that are considered to be of greatest importance for the virulence of the virus."

Which leads to a queasy sense that perhaps the current outbreak of the H1N1 strain of swine flu may be the result of some mad experiment gone awry. Adrian Gibbs, a prominent Australian scientist who collaborated on research that led to the development of the Tamiflu drug, told Bloomberg News "the new strain may have accidentally evolved in eggs scientists use to grow viruses and drugmakers use to make vaccines. Gibbs said he came to his conclusion as part of an effort to trace the virus's origins by analyzing its genetic blueprint."

"The sooner we get to grips with where it's come from, the safer things might become," Gibbs told Bloomberg. "'It could be a mistake' that occurred at a vaccine production facility or the virus could have jumped from a pig to another mammal or a bird before reaching humans, he said."

Gibbs is no crank and his claims, at least initially, were taken seriously by the World Health Organization (WHO). Kenji Fukada, WHO's assistant director-general of health security and environment said the agency is reviewing Gibbs' report. On the other hand, the American Centers for Disease Control in Atlanta dismissed the findings, deciding there is "no evidence" to support the scientist's conclusions.

His research is considered credible and the scientist said his analysis is supported by other researchers, including Richard Webby, a virologist at St. Jude Children's Research Hospital in Memphis who found "the new strain is the product of two distinct lineages of influenza that have circulated among swine in North America and Europe for more than a decade."

Gibbs told the financial publication he saw no evidence that "the swine-derived virus was a deliberate, man-made product." The researcher said, "I don't think it could be a malignant thing. It's much more likely that some random thing has put these two viruses together."

Fukada later said that Gibbs' proposition "didn't fit the evidence." The WHO official added that the organization will need to review Gibbs' research article when it is published, but he indicated that "it is unlikely to change the experts' conclusions."

Perhaps Gibbs is wrong and his findings will be relegated to the sidelines. Having said that however, the danger that H1N1 or some derivative might be weaponized cannot be dismissed out of hand.

Indeed, the Journal of the Royal Society of Medicine was so-alarmed by the prospect that in 2003 they commented, "the possibility for genetic engineering and aerosol transmission [of influenza] suggests an enormous potential for bioterrorism." Unsaid, of course, was the gravest threat posed by such dark research may be state terrorism, more specifically, American state terrorism.

Plum Island

If past is prologue, it might be an instructive exercise to take a short detour down memory lane.

One spooky facility that played a key role in America's Cold War bioweapons programs is the 840-acre Plum Island Animal Disease Center (PIADC). Under the nominal control of the U.S. Department of Agriculture, Plum Island shared close ties with the U.S. Army Medical Research Institute of Infectious Diseases (USAMRIID) at Fort Detrick, Md.

According to a series of striking reports by researcher Mark Sanborne, Plum Island's "spiritual godfather" was none other than one Dr. Erich Traub, "a Nazi scientist with a fascinating history." Traub spent the pre-war years as a scientific fellow at the Rockefeller Institute in Princeton, N.J., "studying bacteriology and virology, while still finding time to hang out at Camp Sigfried, headquarters of the American Nazi movement in Yaphank, Long Island, 30 miles west of Plum Island."

Citing evidence uncovered by researcher by Michael Christopher Carroll in his exposé Lab 257, when war broke out, Traub returned to Germany and became the head of Insel Riems, the Nazi state's secret biological warfare research facility located on an island in the Baltic Sea. A fanatical Nazi, Traub tested germ and viral sprays over the occupied Soviet Union "while reporting directly to Heinrich Himmler."

With a CV such as this one would have expected Traub to have landed in prison or at the end of a rope. Think again!

After the war Traub worked briefly for the Soviets before escaping into the embrace of Operation Paperclip, Washington's covert employment program for useful Nazi scientists. As Werner von Braun was to rockets, Traub was to germs: He promptly went to work for the Naval Medical Research Institute and gave operational advice to the CIA and the biowarriors at Fort Detrick. Indeed, his detailed description of his work at Insel Riems probably helped inspire the selection of Plum Island by the Army: both the German and U.S. facilities were situated on islands where the prevailing winds blew (mostly) out to sea. (Mark Sanborne, "'Bionoia' Part 3: The Mystery of Plum Island: Nazis, Ticks and Weapons of Mass Infection," World War 4 Report, No. 121, May 1, 2006)

But that's all in the past, right? Well, not entirely...

Carroll builds a compelling case that the 1975 outbreak and subsequent pandemic spread of Lyme Disease, a tick-borne pathogen first identified in Old Lyme, Connecticut "just 10 miles across Long Island Sound from Plum Island," may have originated when a secret bioweapons experiment went awry.

Since its 1975 appearance nearly 300,000 cases have been reported in 49 states, although given its mimetic abilities and confusing, multi-symptom manifestations, the CDC estimates that only one in 10 cases are recognized as such, which means potentially some three million Americans may have been infected by the pathogen.

Indeed, what makes Lyme the perfect cover as a bioweapon is its capacity as "a devious, multi-systemic, inflammatory syndrome that mimics other illnesses by encompassing a range of afflictions, including chronic and crippling pain and fatigue that untreated can spread to organs and the central nervous system, causing depression, palsy, memory loss, psychosis, and even encephalitis and death," Sanborne grimly informs us.

Why then, would America's biowarriors concern themselves with a disease that "incapacitates but rarely kills" its victims? According to Sanborne, "the logic is brutally simple." Drawing an analogy between how a wounded soldier puts greater stress on an army than a dead one, "gradually sickening a population places greater economic and social stress on a society than simply killing a limited number of people with a more direct and virulent attack."

And if such a disease can be transmitted via a natural vector like ticks or mosquitoes that already possess built-in plausible deniability so to speak "and can confuse medical authorities by presenting a broad array of symptoms that mimic other conditions (Bb, like its more famous relative syphilis, has been called the 'Great Imitator'), then so much the better," Sanborne wrote.

Carroll discovered during his research that entomologist Dr. Richard Endris and African swine fever team leader Dr. William Hess, traveled to Cameroon and other parts of Africa on "tick-hunting safaris." By the time the pair had finished their collection, they had reared "over 200,000 hard and soft ticks of multiple species."

Lab containment practices were cited as "unsafe" by outside consultants who "strongly recommended" the construction of a "modern, approved insectory be undertaken for future research." (emphasis in original) The pair were fired in 1988 and the tick colony destroyed, but the question remains: were the ticks already out of the bag?

There is also evidence that Plum Island researchers experimented with more than ticks. Carroll averred,

Dr. Endris also conducted experiments with sand flies on Plum Island in 1987 to test transmission of leishmaniasis, a bacterial ailment that if left untreated, has a human mortality rate of almost 100 percent. It is characterized by irregular bouts of fever, substantial weight loss, and swelling of the spleen and liver. The work was performed under contract for Fort Detrick, and serves as another example of a deadly germ warfare agent worked on at Plum Island for the Army, with no public knowledge or public safety precautions taken. (Michael Christopher Carroll, Lab 257: The Disturbing Story of the Government's Secret Germ Laboratory, New York: HarperCollins Publishers, 2005, p. 24)

Like other parts of America's bioweapons-industrial complex, disease outbreaks and subsequent cover-ups go hand in hand. The New York Times reported in 2004 that "the highly contagious foot and mouth virus had briefly spread within the Plum Island Animal Disease Center in two previously undisclosed incidents earlier this summer."

Fear not, lab spokesperson Donald W. Tighe told the paper "the virus had remained within the laboratory's sealed biocontainment area. He said there had been no risk to humans or animals inside or outside the laboratory." An investigation "is continuing." Alarmingly, in 1991, Hurricane Bob knocked out power on the island for several hours and disabled the air pressure systems that contained the viruses. At the time, lab spokespersons assured the public "they were safe."

Plans are afoot to close the facility. Global Security Newswire reported in February that the Department of Homeland Security is planning a new, $450 million facility to be built on the Kansas State University campus.

However, The New York Times revealed that "additional costs" would bring the total to about $630 million." The National Bio and Agro-Defense Facility (NBADF) would have "safety built into every square inch," DHS Secretary Janet Napolitano assured critics.

Coming to a City Near You!

Despite lax oversight and a veritable $50 billion ocean of cash washing over universities, corporations and the military, since 2002 the National Institutes of Health (NIH) has spent billions on the construction of new BSL-3 and BSL-4 facilities. More are planned, including those already under construction in major U.S. cities.

One Boston resident, alarmed by the prospect that Boston University Medical Center officials were building "a biological defense laboratory in one of the city's poorest neighborhoods" told the Los Angeles Times, "We heard anthrax and Roxbury-South End," she recalled. "Then we heard Ebola. The last thing we heard was bubonic plague. We looked at each other and said, 'No way are they bringing that ... into our community.'"

Seven years later, the $198-million lab complex stands completed between an apartment building and a flower market. But state and federal lawsuits by anxious residents, backed by skeptical scientists, have blocked the opening until late next year at the earliest.

The battle marks the first major setback in the vast growth since the Sept. 11, 2001, terrorist attacks of labs authorized to research the world's most dangerous diseases. It also underscores a growing debate over the safety and security of such labs--and whether so many are needed.
(Bob Drogin, "Biodefense Labs Make Bad Neighbors, Residents Say," Los Angeles Times, May 17, 2009)

Working class Boston residents aren't the only people alarmed by the explosive growth of such facilities.

According to a 2008 University of California budget document the Board of Regents recommended the allocation of $3,998,000 for a project to renovate and "upgrade" the existing laboratory facility "for programs that require Bio-safety Level 3 (BSL3) containment" on the U.C. Davis campus.

With students and workers reeling under draconian state budget cuts, out-of-control fee hikes and mass layoffs, why would the State of California waste nearly $4 million for such a facility? "The BSL3 space is needed" we are informed, "for research programs utilizing infectious and pathogenic organisms." Indeed, "the facility would be designed to accommodate research studies involving in-vitro experimentation utilizing infected avian, murine, arthropod hosts, and the development of genetic markers for a wide range of disease agents that require BSL3 containment."

But as with most of America's bioweapons-industrial complex, illicit and illegal research is carried out with little or no oversight.

The antinuclear Bay Area watchdog group Tri-Valley CAREs (TVC), has been monitoring and protesting the expansion of America's nuclear weapons complex for decades, with a particular focus on the Lawrence Livermore National Laboratory (LLNL).

An ubiquitous "public-private partner" of the U.S. national security state, LLNL is a "limited liability corporation" comprised of five partners: the University of California, Bechtel, BWX Technologies, Washington Group International and Battelle--all heavy-hitters in the biotech, construction, defense, energy, nuclear and security worlds.

According to TVC, the group obtained government documents as a result of Freedom of Information Act litigation demonstrating that LLNL had violated federal regulations and had carried out "restricted experiments" that were discovered by the Centers of Disease Control inspection in August 2005. CDC, the Department of Energy and LLNL covered up the inspector's report.

Restricted experiments are experiments utilizing recombinant DNA that involve the deliberate transfer of a drug resistance trait to select agents that are not known to acquire the trait naturally. Select agents, which include anthrax and plague, are biological agents and toxins having the potential to pose a severe threat to public health and safety.

Because of the dangers involved in transferring drug resistance to select agents, restricted experiments require approval from the Secretary of the Department of Health and Human Services. Livermore Lab did not have that approval, but ran the experiments anyway.
("Livermore Lab Caught Conducting Illegal Restricted Bio-Experiments," Tri-Valley CAREs, Press Release, May 26, 2009)

According to the watchdog group, the experiments were carried out by the lab at the same time of the accidental release of anthrax in August-September 2005. Five individuals were exposed to the deadly pathogen and a $450,000 fine was levied against the facility. TVC noted that "the relevant details of the 2005 anthrax accident were kept from the public at the time, just as happened with the illegal experiments that are coming to light today."

LLNL has opened a BSL-3 facility and is planning to experiment with pathogens that can be used as offensive weapons. Activities contemplated include, "aerosolizing (spraying) pathogens such as plague, tularemia and Q fever, in addition to anthrax. Moreover, government documents disclose that planned experiments in the BSL-3 include genetic modification and potentially novel manipulation of viruses, prions and other agents."

What of LLNL's close partner, Battelle Memorial? According to a blurb on their web site, the firm's national security brief includes what they euphemistically call "vaccine and therapeutic product development." Battelle "specialists" at their Aberdeen, Maryland research facility (adjacent to USAMRIID's Ft. Detrick bioweapons complex) "study aerosolized microorganisms that may be possibly used in terrorist attacks."

Indeed, Ft, Detrick is currently undergoing the largest expansion in its history. Investigative journalists Bob Coen and Eric Nadler revealed in Dead Silence: Fear and Terror on the Anthrax Trail that the recently-opened "National Biodefense Analysis Countermeasures Center ... contains heavily guarded and hermetically sealed chambers in which scientists will simulate terrorist attacks and use lethal germs and toxins."

Coen and Nadler aver, "this, remember, is the facility that officialdom claims was the source of the only significant germ war attack on US soil." Conveniently enough, "Battelle has the $250 million contract to manage the operation."

But the journalists uncovered more, much more than insipid government pronouncements on "biodefense." During a interview with constitutional law scholar Francis Boyle, a University of Illinois professor and acknowledged expert on the Biological Weapons Convention, Boyle told the investigative sleuths that the "Pentagon is ready to wage anthrax war."

"Look at the Department of Defense's Chemical and Biological Defense Program Report to Congress, April 2007, page 22, Table 2-5. Information Systems Modernization Strategy, Mid FY09-13," Boyle told Coen and Nadler.

"Here you find a study" Boyle asserted, that estimates the "human effects from a 5,000 weapon worldwide strike; to predict fatalities and incapacitation, both initial and delayed and to accommodate population moves including area evacuations or sheltering in place. Now how does that strike you?"

Sounds like business as usual!
American Dream
 
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Postby nashvillebrook » Sun Jul 26, 2009 7:19 pm

Bionoia Part 3 The Mystery of Plum Island: Nazis, Ticks and Weapons of Mass Infection

by Mark Sanborne
In Part 2 of this series, which ran in our February issue, journalist
and researcher Mark Sanborne looked back at how the US, which now
hypes the threat of "bio-terrorism" to justify gutting the Biological
Weapons Convention, has actually spearheaded the development of
biological weapons-and their use against civilian populations. In this
new installment, Sanborne explores the possibility that unusual
outbreaks of exotic diseases within the United States have been linked
to the Pentagon's bio-warfare experiments-including some overseen by
former Nazis. The closing installments will explore the survival of
the secretive Cold War biowar apparatus in both the US and Russia, and
its links to the new wave of biological threats.


If covert elements of the U.S. government have indeed been bombarding
Cuba for over four decades with diseases aimed primarily at animals
and crops, as discussed in Part 2 of this series, where might such
bioagents have been developed? One likely suspect is Plum Island, the
site where, during the early years of the Cold War, germs and viruses
that could be used to wipe out Soviet livestock were cultivated.
Located less than two miles off the North Fork of Long Island and only
six miles from Connecticut, the 840-acre Plum Island Animal Disease
Center was established after World War II. Initially run by the Army,
the facility was put under nominal control of the U.S. Department of
Agriculture (USDA) in the 1950s.

The PIADC was dubbed "the safest lab in the world" and tasked with
studying diseases that could threaten the nation's livestock-which it
did, effectively. But from the beginning Plum Island also played a key
role in the U.S. biowarfare program and shared close ties with Fort
Detrick, MD, the Army's biowar HQ.

This long-suspected nexus was confirmed in Cold War records
declassified in 1993. According to the documents, when calling for a
major biowarfare test in the early 1950s, the Joint Chiefs of Staff
stated: "Steps should be taken to make certain adequate facilities are
available, including those at Fort Detrick, Dugway Proving Ground
[Utah], Fort Terry [Plum Island] and an island testing area." ("Plum
Island's shadowy past: Once-secret documents reveal lab's mission was
germ warfare," Newsday, Nov. 21, 1993.)

"In many cases there were only maybe five people who knew what was
going on in weapons research [at Plum Island]. People in one lab
didn't know what happened in the next lab, and they didn't ask," said
Norman Covert, the aptly named base historian at Fort Detrick.

AGAIN WITH THE NAZIS?

And just to make it officially nefarious: it turns out Plum Island has
Nazi connections. Former U.S. Justice Department prosecutor and Nazi-
hunter John Loftus wrote his 1982 book The Belarus Secret: "Even more
disturbing are the records of the Nazi germ warfare scientists who
came to America. They experimented with poison ticks dropped from
planes to spread rare diseases. I have received some information
suggesting that the U.S. tested some of these poison ticks on the Plum
Island artillery range off the coast of Connecticut during the early
1950s...
Most of the germ warfare records have been shredded, but
there is a top secret U.S. document confirming that 'clandestine
attacks on crops and animals' took place at this time."

More recently, other details emerged in Lab 257: The Disturbing Story
of the Government's Secret Plum Island Germ Laboratory
by Long Island lawyer Michael Christopher Carroll, who spent six years researching the topic. His explosive book actually prompted a lengthy article in the New York Times ("Heaping More Dirt on Plum Island," Feb. 15, 2004). Though meant as a debunking-aside from Carroll, all seven
people interviewed were critics or skeptics-in the Times' perverse
tradition, a lot of interesting information was revealed to its
mainstream readers. But not all of the establishment took the party
line: Former New York Gov. Mario Cuomo endorsed the book as
"brilliant" and a "carefully researched, chilling expose of potential
catastrophe."


Most of the controversy centered around Carroll's informed speculation
that Plum Island may have been the source of a series of epidemics
over the decades: outbreaks of Dutch duck plague that almost wiped out
Long Island's duck industry in the 1960s, the insidious appearance and
spread of Lyme disease in the 1970s and 1980s
, a mystery infection
that killed most of the Long Island Sound's lobsters in 1999, and in
the same year the arrival of West Nile virus in the New York
metropolitan area, which claimed a number of lives and prompted
authorities to repeatedly spray the city with malathion. Allaying
potential public fears over such verboten ideas
was a main reason the
Times devoted so many inches of newsprint to damage control; the
article mentioned the Nazi angle only in passing.

It turns out that the spiritual godfather of Plum Island was one Dr.
Erich Traub, a Nazi scientist with a fascinating history, according to
Carroll's well-documented account. He spent the pre-war years in a
scientific fellowship at the Rockefeller Institute in Princeton, N.J.,
studying bacteriology and virology, while still finding time to hang
out at Camp Sigfried, headquarters of the American Nazi movement in Yaphank, Long Island, 30 miles west of Plum Island. He then took his laboratory skills back to Germany where he eventually became chief of Insel Riems, the Nazi's secret biological warfare lab located on an island in the Baltic, supervising the testing of germ and viral sprays over occupied Russia, targeting cattle and reindeer, while reporting
directly to Heinrich Himmler.

After the war Traub worked briefly for the Soviets before escaping
into the embrace of Operation Paperclip, Washington's covert
employment program for useful Nazi scientists. As Werner von Braun was
to rockets, Traub was to germs: He promptly went to work for the Naval
Medical Research Institute and gave operational advice to the CIA and
the biowarriors at Fort Detrick. Indeed, his detailed description of
his work at Insel Riems probably helped inspire the selection of Plum
Island by the Army: both the German and U.S. facilities were situated
on islands where the prevailing winds blew (mostly) out to sea.

VECTOR ANALYSIS

Despite his exceedingly questionable history, Dr. Traub in fact was
twice asked to be director of Plum Island, including by the USDA. He
declined, but was known to have paid at least several official visits
there. He may very well have been one of the Nazi scientists cited by
Loftus who supervised the dropping of infected ticks from planes.
Which brings us to the question of vectors.


In the context of biowarfare and infectious disease generally, a
vector is an organism or agent that carries pathogens from one host to
another. To attack an enemy's agriculture system, such intermediary
vectors aren't always needed: It's often enough to covertly disperse a
pathogen directly on part of a crop and allow the infection to spread
from plant to plant, as anti-Castro agents apparently did in Cuba on a
number of occasions. (The versatile U.S. attack reportedly has also
employed molds, fungi, insect infestations, and other minute pests
targeted at specific crops-all of which, of course, had to be grown
and tested somewhere first.)

However, it's not quite so simple to attack animal and human
populations, which are not stationary targets. Effective aerial
delivery of agents like anthrax or rabbit fever can be affected by
wind and weather, and is more likely to be detected as a deliberate
attack. (Though if it's sprayed on an army of protestors on the
Washington Mall, a possibility discussed in Part 1 -well, that's
apparently another story.)

On the other hand, employing such vectors as mosquitoes, fleas, lice,
and ticks to transmit diseases to targeted populations, while much
slower in effect, can spread a greater variety of infections much more
widely while maintaining a degree of plausible deniability for the
attacker. Thus we should not be surprised that the fruits of Nazi and
Imperial Japanese research and development in this ugly field ended up
in eager U.S. hands after the war.

RETURN TO CUBA

Which bring us to this: Carroll cites an internal 1978 USDA document
titled "African Swine Fever" obtained from an investigation by former
Long Island congressman Thomas Downey. It notes that in research at
Plum Island 1975 and 1976, "the adult stages of Abylomma americanum
and Abylomma cajunense were found to be incapable of harboring and
transmitting African swine fever virus." Translated, that means
scientists had tested the Lone Star tick and the Cayenne tick as
effective vectors for African swine flu
and found them wanting.

A vector is generally thought to be a one-way affair. But while this
particular vector test failed, it also seems to point, paradoxically,
in two directions at once. One is back, once again, to Cuba. Note that
Plum Island's research on suitable vectors for African swine fever
took place midway between unusual outbreaks of that disease in Cuba,
in 1971 and 1979-80, as discussed in Part 2. (And recall that its
appearance in Cuba was a first in the Western hemisphere
.)

Perhaps the U.S. scientists were innocuously testing potential vectors
that could spread the exotic flu to America's pork industry. Or perhaps
-considering Plum Island's longstanding connections to Fort Detrick-
the tests were actually designed to find a new vector to transmit the
virus once again to Cuba, which coincidentally did suffer another
outbreak a few years later. In any event, whatever vector infected
Cuba's pigs with African swine fever in 1971 and 1979, it's safe to
say it wasn't the Lone Star or Cayenne ticks.

But is that the end of the infected tick story? Unfortunately, no.
Because the failed Plum Island vector test also points in another
possible direction, right back into the heart of what our political-
warrior class now likes to call the Homeland. And rather than riding
off ineffectually into the sunset, the Lone Star tick has gone on to a
key supporting role in yet another biomystery.

THE PANDEMIC THAT DARE NOT SPEAK ITS NAME

In 1975, a strange disease broke out in Old Lyme, Connecticut, just 10
miles across Long Island Sound from Plum Island. Often initially
characterized by a red rash and swollen joints, it afflicted an
original cluster of 50 victims, many of them children, who were at
first misdiagnosed as having juvenile rheumatoid arthritis.

It turns out that "Lyme disease"-as it came to be called as cases
mounted and spread in the years that followed-is a devious, multi-
systemic, inflammatory syndrome that mimics other illnesses by
encompassing a range of afflictions, including chronic and crippling
pain and fatigue that untreated can spread to organs and the central
nervous system, causing depression, palsy, memory loss, psychosis, and
even encephalitis and death.

Such severe outcomes might surprise many Americans, most of whom have heard of Lyme disease but because of the current lack of media
attention probably think it's no big deal-unless they know someone who
suffers from it. Well guess what? With a quarter century behind the
outbreak, Lyme is now the most common vector-borne infection in the
United States, and the most common tick-born illness in the world.

Yes, you heard that right.

After spreading out from "ground zero" in the Long Island Sound area,
as of mid-April 2006, a total of 267,779 domestic cases of Lyme in 49
states had been reported to the federal Centers for Disease Control.

Some experts estimate that, due to Lyme's confusing multiple
manifestations, at most only one in 10 cases are recognized and
reported to the CDC
, so that the total number of victims could be more
than 2.68 million. On top of that, a study predicts a one-third
increase in the number of cases per year in the U.S. over the 10-year
period from 2002 to 2012.

A TICK WITH A HISTORY

So what's going on? Where did this weird bug-which, leaving aside its
suspicious proximity to Plum Island, seemed to emerge from nowhere-
supposedly come from? Its history is intriguing. In 1982, National
Institutes of Health researcher Dr. Willy Burgdorfer isolated and
identified spirochetes (a form of bacteria) of the genus Borrelia from
the gut of infected Ixodes scapularis (commonly known as deer ticks)
as the etiological agent of Lyme disease. It was dubbed Borrelia
burgdorferi (Bb), and the good doctor ruefully said of his discovery:
"It's a helluva bug, and I'm sorry my name is on it!"

However, while Burgdorfer was the first to isolate the insidious
spirochete (which animal studies suggest in some cases can worm its
way deep inside tendons, muscle, the heart and the brain inside a
week), earlier incarnations of the disease had been studied in Europe
since the late 19th century. By the 1930s, it was known to cause
neurological and psychiatric problems and the tiny Ixodes tick was
suggested as a vector. By mid-century doctors were using new
antibiotic treatments with some success.

But while the disease caused by the Bb bacteria was known in Europe,
it did not appear to constitute a major health problem. It was even
less of an issue on the other side of the Atlantic: Although Bb and
related bacterial strains are thought to have long been present in
North America, the only official case reported in the U.S. before the
Connecticut outbreak occurred in Wisconsin in 1970, when a hunter
became infected from a tick bite.

So what changed in the 1970s to kick-start what has since become a
pandemic, both here and in Europe? (Though the P-word is never used in
reference to Lyme, as opposed to bird flu, which is still only a
potential pandemic.) Or are we to believe that Bb has been infecting
people all along but somehow it just wasn't being noticed? A similar
argument has been advanced by apologists for the medical-industrial
complex who maintain that the recent explosion of autism was simply
the result of better detection and recognition of the condition,
rather than being largely caused by mercury-laced vaccines, as many
now suspect.

THE INVADERS

Dr. Alan G. Barbour, who worked closely with Burgdorfer in the
identification of Bb, co-wrote an article with Durland Fish in 1993
that made an interesting case for how the modern outbreak of Lyme
disease may have occurred. They suggested that Bb infections were a
fact of life in early American history that went largely unnoticed
amid the harshness of frontier life:

"The generally benign nature [!] of acute B. burgdorferi infection
relative to the debilitating and fatal effects of diseases plaguing
North Americans through the 19th century may have contributed to its
obscurity until a cluster of cases of childhood arthritis first
brought it to wider attention on this continent. The ecological
changes in the northeastern and midwestern United States during this
century are responsible for the recent emergence of Lyme disease as a
public health problem."


They argue that mass deforestation of the Northeast due to the
clearing of land for agriculture and settlement in the 19th and early
20th century resulted in a collapse of white-tailed deer populations,
the primary carriers of the I. scapularis tick, and hence the tick
itself became too scarce to infect people with Bb. The authors further
theorize that Long Island served as a refuge for relict populations of
deer in the area. Then, as land-use patterns changed in the latter
half of the 20th century, woodlands and forests recovered in the
Northeast, along with deer and deer ticks:

"The invasion by I. scapularis of the increasingly reforested mainland from island refuges initiated the current epidemic of Lyme disease in the Northeast ... There is evidence that several independent mainland invasions [mainly from Long Island] by I. scapularis took place,
resulting in early Lyme disease foci in central New Jersey, mainland
Westchester County, N.Y., southeastern Connecticut, and eastern
Massachusetts."


So science seems clear on the fact that Long Island was the source of
the modern outbreak of Lyme disease, but the devil is in the details.

The key problem with Barbour and Fish's scenario is that it treats
pre-1975 Long Island like some kind of lost world, an offshore
wilderness Eden where remnant deer lived free of human interaction. In
fact, the island's deer population, concentrated in eastern Suffolk
County, has long lived close by people, many of whom were certainly
exposed to deer tick bites over the years. So why were there no
reports of the disease on Long Island in the decades before the
outbreak in Connecticut? And why, in the wake of that outbreak across
the Sound, did Suffolk County-home of Plum Island-quickly develop one
of the highest rates of Lyme disease in the country?

This writer grew up in western Suffolk County in the 1960s and '70s,
and spent plenty of time exploring the woods, and was bitten by plenty
of ticks. But they were the types of tick you can easily see and feel
crawling on your skin, and thus usually could be picked off before
they began engorging themselves in earnest on one's blood.

Fortunately, there were no deer or deer ticks in my neck of the woods.
So it came as quite a shock to learn in the late '70s of the sudden
existence, just a few dozen miles to the east, of infected ticks that
were almost invisible--literally the size of a pinhead--and had the
ability to make an unlucky hiker's life into a living hell. Our tiny
friend I. Scapularis is indeed the perfect covert agent: it does its
dirty work quickly and disappears before you know it's there, usually
leaving behind a telltale rash and a very questionable prognosis.

WOUND, DON'T KILL

Okay, enough beating around the real and metaphorical bushes. Is there
any actual evidence that Lyme disease could be the outcome of
biological warfare research at Plum Island that, either accidentally
or otherwise, escaped into the outside world? In fact, the evidence
seems quite suggestive, especially when compared to the shaky logic of
the official story.

Some might ask: Why would biowarriors be interested in studying a
disease agent like Borrelia burgdorferi that incapacitates but rarely
kills its victims? Actually, for all the attention focused on deadly
pathogens like anthrax, plague, and rabbit fever, the biowar
establishments of various powers have also long been interested in
agents that can slowly stricken and debilitate a civilian population.

The logic is brutally simple: just as a wounded soldier puts more
logistical strain on an army than a dead one does, gradually sickening
a population places greater economic and social stress on a society
than simply killing a limited number of people with a more direct and
virulent attack.
If the disease agent can be transmitted via a
"natural" vector like ticks or mosquitoes, providing plausible
deniability, and can confuse medical authorities by presenting a broad
array of symptoms that mimic other conditions (Bb, like its more
famous relative syphilis, has been called the "Great Imitator"), then
so much the better.

Imperial Japan's infamous Unit 731 biowar outfit, discussed in Part 2,
reportedly conducted experiments with the Borelia genus, the results
of which likely fell into U.S. hands after the war. However, there is
no documentary evidence that indicates Plum Island researchers ever
worked with Bb -after all, it is primarily a disease of humans, not
animals. On the other hand, if the bacteria were being secretly
studied (or worse, "weaponized") at the lab and introduced to ticks
for vector tests, there are any number of ways tick-borne Bb could
have escaped to the mainland: from deer--which are able to swim to and
from the island--to birds, or even an inadvertently infected lab
worker. (Assuming, of course, it wasn't released on purpose as part of
some sinister test.)

Since the Lyme outbreak, scientists claim to have documented the
presence of Bb in I. scapularis museum specimens collected in the late
1940s from Shelter Island and other parts of Long Island close by Plum
Island. This is presumed to be evidence that the spirochete was pre-
existing in the area and was not "engineered" in a lab in the 1970s.

But note that the period the tick specimens were collected is
suspiciously close to the time when Nazi scientists may have
"experimented with poison ticks dropped from planes to spread rare
diseases" at Plum Island.

GIVING NATURE A HAND

The question then arises: Are the unusual characteristics of Bb solely
the result of natural evolutionary processes, or were they helped
along by the hand of man? Speaking more generally, here's what Col.
Oliver Fellowes, a founding father of Plum Island who was transferred
from Fort Detrick in 1952, had to say: "We were always looking for a
way to camouflage a strain so that it would be so difficult to detect
and identify that, by the time the enemy had done so, the disease
would have done the damage." (Unit 731 by Peter Williams and David
Wallace, Hodder & Stoughton, London, 1989.)

Wait, it gets better. On July 1, 1969, Dr. Donald MacArthur, director
of the Defense Advanced Research Project Agency, testified before a
subcommittee of the House Appropriations Committee. He had this
exchange with Rep. Robert Sikes of Florida:

DR. MACARTHUR: There are two things about the biological agent field I would like to mention. One is the possibility of technology surprise.
Molecular biology is a field that is advancing very rapidly and
eminent biologists believe that within a period of five to 10 years it
would be possible to produce a synthetic biological agent, an agent
that does not naturally exist and for which no natural immunity could
have been acquired.
REP. SIKES: Are we doing any work in that field?
DR. MACARTHUR: We are not.
REP. SIKES: Why not? Lack of money or lack of interest?
DR. MACARTHUR: Certainly not lack of interest.


MacArthur's chilling testimony can be seen as the Rosetta Stone of
bionoia, and will be discussed in greater detail in a later
installment. But we don't need it for confirmation that something like
Lyme disease can be considered a biological warfare agent--we have it
straight from the source, namely the U.S. government. On Nov. 15,
2005, the Associated Press reported:

"A new research lab for bioterrorism opened Monday at the University of Texas at San Antonio. The $10.6 million Margaret Batts Tobin
Laboratory Building will provide a 22,000-square-foot facility to
study such diseases as anthrax, tularemia, cholera, lyme disease,
desert valley fever and other parasitic and fungal diseases. The
Centers for Disease Control and Prevention identified these diseases
as potential bioterrorism agents."


That, it would seem, makes it official. Among those who took note of
this matter-of-fact admission was Dr. Virginia Sherr, who, in a letter
to the editor published Nov. 22, 2005 in the online edition of the
Lancet medical journal, wrote:

"[The] concern is the overriding significance of an invisibilized but
nonetheless serious infection caused by an extraordinarily complex
neurotropic spirochete. Its pandemic is approaching severity that was
experienced throughout the world in the Spanish Flu of 1918. The
causative spirochete is, of course, less immediately fatal than was
the virus of that epidemic, but it is deadly, nonetheless, to the
human brain.
The fact that the causative spirochete, B. burgdorferi,
is being studied as an agent of biowarfare in the USA adds impetus to
a need for quick education of most of the world's academic physicians
as to what has been sensed at the clinical level for a long time: we
are dealing here with a formidable 'smart stealth' type of bacteria
that is hard to eradicate--one that does extreme damage to psyche and
soma if not treated aggressively over the long term when missed in the
first days following inoculation by the vector... Organized Medicine
has mostly ignored or deserted the field of neuro-Lyme's currently
immense proportions, internationally."


THE REVENGE OF TEXAS

Whither Plum Island? According an Aug. 28, 2005, story in Newsday,
"Plum Island's Future Up In The Air," the federal government plans to
replace the existing facility on the island with a more secure one or
relocate to a higher-security level research lab elsewhere by 2011.
"The Plum Island facility was built in the 1950s and is nearing the
end of its life cycle," according to the Deptartment of Homeland
Security. Glad to hear those guys are on the case.

Ah, but what about the Lone Star tick and its failed vector test back
in 1975? Aside from that curious coincidence with Cuba, the documented
research also appears to have something to say about events much
closer to home. It demonstrates that Plum Island researchers were
infecting Abylomma americanum with various bioagents to see if they
could be successfully vectored to other species.
(In this case pigs,
but swine are often used as stand-ins for humans in medical
experiments.)

That is a matter of some interest because, while the I. Scapularis
deer tick is the major vector for Lyme disease in the Northeast, the
Lone Star tick has also been found to be a carrier of spirochetes.

There is some debate about whether A. americanum can transmit Bb to
humans. Researchers say the tick carries a slightly different bacteria
that they've dubbed Borrelia lonestari, which may or may not cause a
"new" Lyme-related ailment called Masters disease, identified in 1991
in Missouri.

The fact that two different ticks carry their own versions of an
unusual spirochete bio-agent is suspicious enough--designer bugs,
perhaps? (Check out this unintentional smoking gun in Barbour and
Fish's article: "The presence of spirochetes similar to B. burgdorferi
in A. americanum in areas where competent vectors are absent is
inexplicable.")

But here's the real kicker: The Lone Star is a warm-weather tick that is prevalent in the Southeast and until recently was mostly unknown in the colder Northeast. Now it has reached as far north as-you guessed it-Long Island, New Jersey, and Connecticut. (Though perhaps the word should not be "reached" but "released.")

A. americanum now makes up 5% of the overall tick population in the
region, though there are greater concentrations in some areas than
others. (Researchers combing the woods in New Jersey have found 2,000
to 3,000 Lone Star ticks within one hour.) When did these little
devils start being noticed up here in large numbers? Yup: In the wake
of the outbreak of Lyme disease--though there are reports that the
initial invaders may have "arrived" as far back as the 1950s, just as
things were getting underway at Plum Island.

And yes, Abylomma americanum, as it's nickname suggests, has a special
association with the Lone Star State. Another import from Texas that
the rest of the country probably could have done without.


RESOURCES:
Lyme Disease Foundation
http://www.lyme.org/
"The Biological and Social Phenomenon of Lyme Disease," Barbour and
Fish, Association for the Advancement of Science, June 1993
http://info.med.yale.edu/eph/vectorbio/ ... urFish.pdf
Dr. Donald MacArthur, Congressional testimony, July 1, 1969
http://panindigan.tripod.com/aidsdodhear.html
See also:
"Bionoia," Pt. 2, WW4 REPORT #118
-------------------
Special to WORLD WAR 4 REPORT, May 1, 2006
Reprinting permissible with attribution[/b]
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Postby seemslikeadream » Sun Jul 26, 2009 7:26 pm

Thanks for posting

Full movie can be seen here

http://www.220.ro/gif3e9pADl/28-Days-Later
Mazars and Deutsche Bank could have ended this nightmare before it started.
They could still get him out of office.
But instead, they want mass death.
Don’t forget that.
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Postby Hugh Manatee Wins » Sun Jul 26, 2009 10:46 pm

*gasp* Makes me wish I couldn't read...

seemslikeadream wrote:Thanks for posting

Full movie can be seen here
......

http://kids.yahoo.com/parents/blog/1006 ... landing/24

Image

"Moments of humor and absurdity, usually in the guise of the two FBI agents assigned to locate Froggy Doo, keep the movie moving at a brisk pace."
CIA runs mainstream media since WWII:
news rooms, movies/TV, publishing
...
Disney is CIA for kidz!
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Postby StarmanSkye » Mon Jul 27, 2009 2:43 am

Great documentary series by Dr. Horowitz who affirms and adds more details to many of the issues and reports raised in the previous articles.


In Lies We Trust: Part 1/15
http://www.youtube.com/watch?v=8R2hmC6uav8

This feature length documentary about medical madness, cloaked in bioterrorism preparedness, will awaken the brain dead. It exposes health officials, directed by the Central Intelligence Agency (CIA), for conducting a War of Terror that is killing millions of unwitting Americans. This urgent life-saving DVD comes without copyright restrictions. Every viewer is encouraged to reproduce and distribute copies to others. Donations to Tetrahedron Films to cover costs and produce more films like this are greatly appreciated online at http://www.inlieswetrust.com or by calling toll free 1-888-508-4787. You can screen the film on behalf of local charities. It was produced by award-winning humanitarian, Dr. Leonard G. Horowitz (http://www.DrLenHorowitz.com), a world-renowned authority in public health education, covert intelligence agency operations, and emerging diseases investigations. He is the author of three American bestsellers, including Emerging Viruses: AIDS; Ebola—Nature, Accident or Intentional? and Healing Codes for the Biological Apocalypse. (Tetrahedron Press; 1-888-508-4787) This monumental film exposes the agents and agencies behind: Hollywood films and the media creating a profitable culture of bioterror; the War on Terrorism used to control populations; the most lucrative war in history—the War on Cancer; the onslaught of dozens of new immunological diseases and deadly flus; the War on AIDS triggered by contaminated vaccines; the anthrax mailings resulting in restricted freedoms, and sales of toxic drugs, deadly vaccines, and more. Documents displayed in film may be viewed online at http://inlieswetrust.com For over 400 of the top Critically important videos see http://netctr.com/media -- Much more at the site. Wake up, get involved, Save the Republic - Your kids, grand kids and your life will depend on what you do from now on. Key words: propaganda, war, terrorism, vaccinations, immunizations, cancer, biological warfare, weapons of mass destruction, pharmaceuticals, AIDS, anthrax, healthcare, Hollywood, CIA, CDC, and FDA
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Biological Warfare and the National Security State: A Chrono

Postby American Dream » Sun Aug 09, 2009 3:18 pm

http://antifascist-calling.blogspot.com ... ional.html

Biological Warfare and the National Security State: A Chronology

The history of bioweapons research in the United States is a history of illicit--and illegal--human experiments.

From the Cold War to the War on Terror, successive American administrations have turned a blind eye on dubious research rightly characterized as having "a little of the Buchenwald touch."

While the phrase may have come from the files of the Atomic Energy Commission as Pulitzer prize-winning journalist Eileen Welsome revealed in her 1999 book, The Plutonium Files, an investigation into secret American medical experiments at the dawn of the nuclear age, it is as relevant today as the United States pours billions of dollars into work on some of the most dangerous pathogens known to exist in nature.

That Cold War securocrats were more than a little concerned with a comparison to unethical Nazi experiments is hardly surprising. After all, with the defeat of the Axis powers came the triumphalist myth-making that America had fought a "good war" and had liberated humanity from the scourge of fascist barbarism.

Never mind that many of America's leading corporations, from General Motors to IBM and from Standard Oil to Chase National Bank, were sympathizers and active collaborators with the Third Reich prior to and even during World War II, as documented by investigative journalists Charles Higham in Trading With The Enemy, and Edwin Black in IBM and the Holocaust. Like much else in American history, these were dirty little secrets best left alone.

Soon enough however, these erstwhile democrats would come to view themselves as mandarins of a new, expanding American Empire for whom everything was permitted. In this context, the recruitment of top German and Japanese scientists who had conducted grisly "medical" experiments whilst waging biological war against China and the Soviet Union would be free of any moralizing or political wavering.

As the Cold War grew hotter and hotter, America's political leadership viewed "former" Nazis and the architects of Japan's Imperial project not as war criminals but allies in a new undertaking: the global roll-back of socialism and the destruction of the Soviet Union by any means necessary.

This tradition is alive and well in 21st century America. With the September 11, 2001 terrorist attacks and subsequent anthrax mailings as a pretext for an aggressive militarist posture, the national security state is ramping-up research for the production of genetically-modified organisms for deployment as new, frightening weapons of war.

According to congressional testimony by Dr. Alan M. Pearson, Director of the Biological and Chemical Weapons Control Program at the Washington D.C.-based Center for Arms Control and Non-Proliferation, with very little in the way of effective oversight or accountability, tens of billions of dollars "have been appropriated for bioweapons-related research and development activities." Pearson reveals that approximately $1.7 billion "has been appropriated for the construction on new high containment facilities for bioweapons-related research."

By high containment facilities I mean facilities that are designed for work with agents that may cause serious or potentially lethal disease through exposure to aerosols (called Biosafety Level 3 or BSL-3 facilities) and facilities that are designed for work with agents that pose a "high individual risk of life-threatening disease, which may be transmitted via the aerosol route and for which there is no available vaccine or therapy" (called Biosafety Level 4 or BSL-4 facilities).

Prior to 2002, there were three significant BSL-4 facilities in the United States. Today twelve are in operation, under construction, or in the planning stage. When completed, there will be in excess of 150,000 square feet of BSL-4 laboratory space (as much space as three football fields). The number of BSL-3 labs is also clearly growing, but ascertaining the amount of growth is difficult in the absence of accurate baseline information. There are at least 600 such facilities in the US.
(Alan M. Pearson, Testimony, "Germs, Viruses, and Secrets: The Silent Proliferation of Bio-Laboratories in the United States," House Energy and Commerce Committee, Subcommittee on Oversight and Investigations, October 2007)

Chillingly, one consequence of this metastatic growth "is that the very labs designed to protect against bioweapons may become a source for them." As the 2001 anthrax attacks amply demonstrated, the threat posed by a biological weapons' incident may be closer to home than any of us care to think. Pearson writes, "Nor should we ignore the possibility that a US biologist may become disgruntled or turn rogue while working in one of these labs."

According to Edward Hammond, the Director of the now-defunct Sunshine Project, while "biological arms control is currently in ... its worst crisis since the signing of the Bioweapons Convention (BWC) in 1972," the American Bioweapons-Industrial Complex has "embarked on the exploitation of biotechnology for weapons development." Indeed, Hammond relates that active programs utilizing genetic engineering techniques have "been employed in offensive biowarfare programs in order to make biowarfare agents more effective."

But increases in state subsidies for such work have generated new risks to the public. A recent Government Accountability Office (GAO) report faulted the Centers for Disease Control and Prevention (CDC) for lax security at three of the nation's five BSL-4 labs currently in operation that "handle the world's most dangerous agents and toxins that cause incurable and deadly diseases." Agents such as Ebola, Marburg and smallpox are routinely studied at these facilities. And yet, as GAO auditors found,

Select agent regulations do not mandate that specific perimeter security controls be present at BSL-4 labs, resulting in a significant difference in perimeter security between the nation's five labs. According to the regulations, each lab must implement a security plan that is sufficient to safeguard select agents against unauthorized access, theft, loss, or release. However, there are no specific perimeter security controls that must be in place at every BSL-4 lab. While three labs had all or nearly all of the key security controls we assessed, our September 2008 report demonstrated that two labs had a significant lack of these controls. (Government Accountability Office, Biosafety Laboratories: BSL-4 Laboratories Improved Perimeter Security Despite Limited Action by CDC, GAO-09-851, July 2009)

As Global Security Newswire revealed in June, a "recently completed inventory at a major U.S. Army biodefense facility found nearly 10,000 more vials of potentially lethal pathogens than were known to be stored at the site."

The 9,220 samples--which included the bacterial agents that cause plague, anthrax and tularemia; Venezuelan, Eastern and Western equine encephalitis viruses; Rift valley fever virus; Junin virus; Ebola virus; and botulinum neurotoxins--were found during a four-month inventory at the U.S. Army Medical Research Institute of Infectious Diseases at Fort Detrick, Md., according to Col. Mark Kortepeter, the center's deputy commander. (Martin Matishak, "Thousands of Uncounted Disease Samples Found at Army Biodefense Lab," Global Security Newswire, June 18, 2009)

The GSN report states that while "half of the newfound material was destroyed after being recorded," inventory control officer Sam Edwin told reporters that "the other half was deemed worthy for further scientific use, cataloged, and stored in the center's containment freezers."

More pertinently, what happens when the state itself turns "rogue" and under cover of national security and the endless "war on terror" creates the "acute risk" in the form of out-of-control laboratories "designed to protect against bioweapons" that instead, have "become a source for them"?

Bioweapons and National Security: A Chronology

Source Notes: This chronology has drawn from dozens of books, articles and declassified government documents in its preparation. Notable in this regard is Michael Christopher Carroll's Lab 257: The Disturbing Story of the Government's Secret Germ Laboratory; Linda Hunt, Secret Agenda; Bob Coen and Eric Nadler, Dead Silence: Fear and Terror on the Anthrax Trail; the National Security Archive's documentary history of U.S. Biological Warfare programs and The Sunshine Project.

* August 1945: Operation Paperclip, an Office of Strategic Services (OSS) program to import top Nazi scientists into the United States. Linda Hunt relates in her book, Secret Agenda, that Reich Health Leader (Reichsgesundheitsführer) Dr. Kurt Blome, was saved from the gallows due to American intervention. Blome admitted he had worked on Nazi bacteriological warfare projects and had experimented on concentration camp prisoners with bubonic plague and sarin gas at Auschwitz. After his acquittal at the 1947 Nuremberg Doctors' Trial, Blome was recruited by the U.S. Army Chemical Corps and advised the Pentagon on biological warfare. Walter Paul Emil Schreiber, a Wehrmacht general who assigned doctors to experiment on concentration camp prisoners and disbursed state funds for such experiments was another Paperclip recruit; in 1951, Schreiber went to work for the U.S. Air Force School of Medicine. Hubertus Strughold, the so-called "father of space medicine" discussed--and carried out--experiments on Dachau inmates who were tortured and killed; Strughold worked for the U.S. Air Force. Erich Traub, a rabid Nazi and the former chief of Heinrich Himmler's Insel Riems, the Nazi state's secret biological warfare research facility defects to the United States. Traub was brought to the U.S. by Paperclip operatives and worked at the Naval Medical Research Institute and gave "operational advice" to the CIA and the biowarriors at Ft. Detrick.

* September 1945: General Shiro Ishii's Unit 731, a secret research group that organized Japan's chemical and biological warfare programs is granted "amnesty" by Supreme Allied Commander in the Pacific, General Douglas MacArthur in exchange for providing America with their voluminous files on biological warfare. All mention of Unit 731 is expunged from the record of The Tokyo War Crimes Tribunal. During the war, Unit 731 conducted grisly experiments, including the vivisection of live prisoners, and carried out germ attacks on Chinese civilians and prisoners of war. According to researcher Sheldon H. Harris in Factories of Death: Japanese Biological Warfare 1932-45 and the American Cover-Up, Unit 731 scientists performed tests on prisoners with plague, cholera, smallpox, botulism and other infectious diseases. Their work led to the development of what was called a defoliation bacilli bomb and a flea bomb used by the Imperial Army to spread bubonic plague across unoccupied areas of China. The deployment of these lethal munitions provided the Imperial Army with the ability to launch devastating biological attacks, infecting agriculture, reservoirs, wells and populated areas with anthrax, plague-infected fleas, typhoid, dysentery and cholera. Rather than being prosecuted as war criminals, Unit 731 alumni became top bioweapons researchers. Ishii himself became an adviser at USAMRIID at Ft. Detrick.

1950: A U.S. Navy ship equipped with spray devices supplied by Ft. Detrick, sprayed serratia marcescens across the San Francisco Bay Area while the ship plied Bay waters. Supposedly a non-pathogenic microorganism, twelve mostly elderly victims die.

* Early 1950s: Army biological weapons research begins at the Plum Island Animal Disease Center (PIADC). Vials of anthrax are transferred from Ft. Detrick to Plum Island. This information is contained in a now declassified report, "Biological Warfare Operations," Research and Development Annual Technical Progress Report, Department of the Army, 1951.

* 1951: Racist experiments are carried out. U.S. Army researchers deliberately expose African-Americans to the fungus Aspergillus fumigatus to discern whether they are more susceptible to infections caused by such organisms than white Europeans. Also in 1951, black workers at the Norfolk Supply Center in Virginia were exposed to crates contaminated with A. fumigatus spores.

* 1952: According to 1977 hearings by the Senate Select Committee on Intelligence and the Subcommittee on Health and Scientific Research into Project MKULTRA, we discover the following: "Under an agreement reached with the Army in 1952, the Special Operations Division (SOD) at Fort Detrick was to assist CIA in developing, testing, and maintaining biological agents and delivery systems. By this agreement, CIA acquired the knowledge, skill, and facilities of the Army to develop biological weapons suited for CIA use."

* 1953: Frank Olson, a chemist with the Army's top secret Special Operations Division at Ft. Detrick was involved with biological weapons research and was tasked to the CIA for work on MKULTRA. In 1953, as Deputy Acting Head of Special Operations for the CIA, Olson is a close associate of psychiatrist William Sargant who was investigating the use of psychoactive drugs as an interrogation tool at Britain's Biological Warfare Centre at Porton Down. After being dosed with LSD without his knowledge by Dr. Sidney Gottlieb, the Agency's liaison to Ft. Detrick, Olson undergoes a severe psychological crisis. The scientist begins questioning the ethics of designing biological organisms as weapons of war. This does not sit well with his Agency and Army superiors. On November 24, 1953, Olson and a CIA minder, Robert Lashbrook, check into New York's Staler Hotel. He never checked out. According to Lashbrook, Olson had thrown himself through the closed shade and window, plunging 170 feet to his death. But because of his knowledge of CIA "terminal experiments" and other horrors conducted under MKULTRA, the Olson family believes the researcher was murdered. When Olson's son Eric has his father's body exhumed in 1994, the forensic scientist in charge of the examination determines that Olson had suffered blunt force trauma to the head prior to his fall through the window; the evidence is called "rankly and starkly suggestive of homicide." Norman G. Cournoyer, one of Olson's closet friends at Ft. Detrick also believes the scientist was murdered. When asked by the Baltimore Sun in 2004 why Olson was killed, Cournoyer said, "To shut him up. ... He wasn't sure we should be in germ warfare, at the end."

* 1955: Following a CIA biowarfare test in Tampa Bay, Florida, the area experiences a sharp rise in cases of Whooping Cough, including 12 deaths. The Agency had released bacteria it had obtained from the U.S. Army's Chemical and Biological Warfare Center at the Dugway Proving Grounds.

* 1956-1958: More racist experiments. The U.S. Army conducted live field tests on poor African-American communities in Savannah, Georgia and Avon Park, Florida. Mosquitoes were released into neighborhoods at ground level by "researchers" or by helicopter; residents were swarmed by the pest; many developed unknown illnesses and some even died. After the tests, Army personnel posing as health workers photographed and tested the victims, then disappeared. While specific details of the experiments remain classified, it has been theorized that a strain of Yellow Fever was used to test its efficacy as a bioweapon.

* 1962: A declassified CIA document obtained by the National Security Archive relates the following: "In November 1962 Mr. [redacted] advised Mr. Lyman Kirkpatrick that he had, at one time, been directed by Mr. Richard Bissell to assume responsibility for a project involving the assassination of Patrice Lumumba, then Premier, Republic of Congo. According to Mr. [redacted] poison was to have been the vehicle as he made reference to having been instructed to see Dr. Sidney Gottlieb in order to procure the appropriate vehicle." Gottlieb was the chief scientific adviser for the CIA's MKULTRA program.

* June 1966: The U.S. Army's Special Operations Division dispenses Bacillus subtilis var niger throughout the New York City subway system. More than a million people were exposed when Army operatives dropped light bulbs filled with the bacteria onto ventilation grates.

* December, 1967: The New York Times reports, "Fatal Virus Found in Wild Ducks on L.I." A virus never seen before in the Western hemisphere, began with ducks in Long Island at a site opposite Plum Island; the virus devastates the area's duck industry and by 1975 has spread across the entire continent.

* 1971: The U.S. Department of Agriculture proclaims that "Plum Island is considered the safest in the world on virus diseases." USDA's proof? "There has never been a disease outbreak among the susceptible animals maintained outside the laboratory since it was established."

* 1975: PIADC begins feeding live viruses to "hard ticks," including the Lone Star tick (never seen outside Texas prior to 1975). The Lone Star tick is a carrier of the Borelia burgdorferi (Bb) bacteria, the causal agent of Lyme Disease. The first cases of the illness are reported in Connecticut, directly across from the facility. Current epidemiological data conclusively demonstrate that the epicenter of all U.S. Lyme Disease cases is Plum Island. It is theorized that deer bitten by infected ticks swam across the narrow waterway separating the island from the mainland.

* September 1978: A PIADC news release relays the following: "Foot and Mouth Disease has been diagnosed in cattle in a pre-experimental animal holding facility at the Plum Island Animal Disease Center." A documented outbreak has occurred.

* 1979: An internal investigation of the FMD incident reveals massive, widespread failures in the containment systems at PIADC. A USDA Committee report recommends that "Lab 101 not be considered as a safe facility in which to do work on exotic disease agents until corrective action is accomplished."

* 1979: Despite containment failures and poor practices, USAMRIID undertakes the investigation of the deadly Zagazig 501 strain of Rift Valley Fever at PIADC. Producing symptoms similar to aerosolized hemorrhagic fevers such as Marburg and Ebola virus, the Army inoculates sheep that should have been destroyed as a result of the FMD outbreak with an experimental Rift Valley Fever vaccine. The experiments are conducted outdoors, in violation of the lab's primary directive prohibiting such work. During a 1977 Rift Valley outbreak in Egypt, some 200,000 people are infected and 700 others die excruciating deaths. A survey of blood serum taken before 1977 proved that the virus was not present in Egypt prior to the epidemic. By 2000, rampant outbreaks of the disease have occurred in Saudi Arabia and Yemen with the virus poised to unfurl its tentacles into Europe.

* 1982: A Federal review begun after the FMD outbreak concludes: "We believe there is a potentially dangerous situation and that without an immediate massive effort to correct deficiencies, a severe accident could result... [L]ack of preventive maintenance, [and] pressures by management to expedite programs have resulted in compromising safety."

* 1983: Six PIADC workers test positive for African Swine Fever virus. The workers are not notified of the test results which are conducted clandestinely during routine annual physical exams.

* 1991: USDA privatizes PIADC. A New Jersey firm, Burns & Roe Services Corporation low bids other competitors and is awarded the contract. In cost-cutting moves, the contractor scales back on safety and security measures in place for decades.

* June 1991: An underground cable supplying Lab 257 shorts out but is not replaced since there is no money left in the budget.

* August 1991: Hurricane Bob, a category 3 storm similar to Hurricane Katrina, slams into Plum Island, knocking down overhead power lines that connect Lab 257. The underground cable which was Lab 257's primary power source has not been repaired. Freezers containing virus samples defrost, air seals on lab doors are breached and animal holding room vents fail. PIADC's "fail safe" mechanism of "air dampers" to seal off the facility also fail. Melted virus samples mix with infected animal waste on lab floors as swarms of mosquitoes fill the facility.

* September 1991: The USDA denies that any system failures occurred during the hurricane. Whistleblowing workers in Lab 257 at the time of the blackout are fired in further cost-cutting moves and several subsequently develop mysterious undiagnosed diseases.

* 1992: The Occupational Safety and Health Administration (OSHA) and the Environmental Protection Agency (EPA) cite PIADC with hundreds of safety violations. When OSHA returned five years later, none of the violations have been corrected and discover 124 new violations.

* July 1992: Although USDA officially denies that PIADC conducts biological warfare research, fourteen officials from the Joint Chiefs of Staff and the Pentagon visit Plum Island. Internal documents reveal that that the visit was "to meet with [Plum Island] staff regarding biological warfare." According to Carroll, "the visitors were part of the Arms Control and Disarmament Agency reviewing the dual-use capabilities of the facility."

* Spring 1995: Lab 257 is closed. Although scheduled to be fully decontaminated and demolished in 1996 Carroll reports: "Lab 257 still stands today, rotting from weathered decay, harboring who knows what deep within."

* August 1999: The first four human cases of West Vile virus, a mosquito-borne pathogen never diagnosed in North America are diagnosed on Long Island. Horse farms within a five-mile radius of one another, directly opposite Plum Island, report horses dying following violent seizures. An investigation reveals that 25% of the horses in this small, localized area test positive for West Nile. The outbreak begins in August 1999 when birds, including half the exotic bird species in the Bronx Zoo begin dying mysteriously. The virus has an affinity for birds and the vector is soon identified as the mosquito. In 1999, the disease was confined to the New York City area, however by 2002, the Centers for Disease Control reports all but 6 of the lower 48 states reported West Nile virus in birds, mosquitos, animals or human populations. CDC estimates that some 200,000 people are infected nationally. During the initial outbreak in 1999, veterinary pathologist Tracey McNamara suspected a casual relationship between the bird die-offs and the human cases; CDC rebuffs her concerns. Through her persistent efforts, it is determined that the virus was indeed West Nile, a pathogen that had never been seen in North America. The CDC announces that West Nile virus was in the nation's blood supply when transplant patients who had no prior exposure to the pathogen develop the disease. The USDA's response? Deny, deny, deny? However, Jim House, a former PIADC scientist, believes that West Nile samples existed prior to 1999 on Plum Island. He told Carroll, "There were samples there, and it wasn't answered clearly to the public. They didn't honestly tell how many samples they had and that's when people started to get upset. When Carroll filed a Freedom of Information Act request for a catalog of germs held in the Plum Island virus library, he was turned down on grounds of "national security."

* September 1999: The New York Times reports that due to "the growing threat of biological terrorism" against America's food supply, USDA "is seeking money to turn the Plum Island Animal Disease Center ... into a top security laboratory where some of the most dangerous diseases known to man or beast can be studied."

* 1999: A Cold War-era document is declassified proving that in the early 1950s USAMRIID shipped twelve vials of weaponized anthrax (enough to kill one million people) to PIADC. In 1993 Newsday revealed that previously unclassified documents demonstrated Pentagon plans to disrupt the Soviet economy by spreading diseases to kill pigs, cattle and horses.

* 1999: Plans to "upgrade" PIADC by building a BSL-4 lab are killed when Congress pulls funding after a public outcry.

* September 2001: After the anthrax attacks, despite USDA denials that anthrax was ever present on the island, FBI investigators include the following questions in their polygraph examination of scientists under investigation: "Have you ever been to Plum Island?" "Do you know anyone who works at Plum Island?" "What do they do there?"

* December 2002: The New York Times reports "a three-hour power failure at the Plum Island Animal Disease Center last weekend renewed concerns about the safety of the high-security government laboratory." According to the Times, "the loss of power and failure of all three backup generators raised fears for the first time that the containment of infectious pathogens could have been seriously compromised at the laboratory."

* June 2003: President George W. Bush transfers control of PIADC to the Department of Homeland Security. The airspace over the island is unrestricted and the gates leading to Lab 101 remain open and unguarded.

* May 2004: In a sign that work on Plum Island is being shifted to "other sites," including those run by private contractors, DHS announces an $18 million grant to study Rift Valley fever, avian influenza and brucellosis.

* August 2004: DHS confirmed that an FMD outbreak "had spread briefly" in "two previously undisclosed incidents earlier this summer," The New York Times reports. A DHS spokesperson said the virus remained "within the laboratory's sealed biocontainment area" and that there "had be no risk" to human or animals. An investigation into the cause "was continuing."

* 2004: At the Medical University of Ohio, a researcher is infected with Valley Fever at the center's BSL-3 facility; Valley Fever is a biological weapons agent.

* February 2005: University of Iowa researchers conduct unauthorized genetic engineering experiments with the select agent Tularemia (rabbit fever). The Sunshine Project reports that researchers mixed genes from Tularemia species and introduced antibiotic resistant characteristics into the samples.

* March 2005: When a containment facility fails, workers at the University of North Carolina at Chapel Hill are exposed to tuberculosis when the BSL-3 "fail-safe" systems malfunction; a blower pushes contaminated air out of the work cabinet, infecting the workroom. The facility had been inspected one month prior to the accident by U.S. Army.

* Summer 2005: At the same Ohio facility a serious accident occurs when workers are infected with an aerosol of Valley Fever.

* October-November 2005: Dozens of samples thought to be harmless are received by the University of California at Berkeley. In fact, they are samples of Rocky Mountain Spotted Fever, a BSL-3 bioweapons agent due to its transmission as an aerosol. The samples are handled without adequate safety precautions; however, the community is never notified of the incident.

* August 2005: The whistleblowing watchdog group Tri-Valley Cares obtains documents in May 2009 proving that the Lawrence Livermore National Laboratory had conducted "restricted experiments" with "select biological agents" at the facility. In 2005, LLNL "inadvertently" released anthrax at the lab in another incident that lab officials attempted to cover-up; five individuals were infected with the deadly pathogen.

* April 2006: Three Texas A&M "biodefense" researchers are infected with Q Fever, a biological weapons agent. Rather than reporting the incident to the CDC as required by law, Texas A&M officials cover-up the accident.

* August 2006: DHS announces that PIADC is "not on the rebuilding list" and a new site to study infectious diseases is being considered.

* January 2009: DHS announces that the new National Bio and Agro-Defense Facility will be built in Manhattan, Kansas.

* July 2009: Government Accountability Office investigators charge that DHS relied on "a rushed, flawed study" to locate the $700 million research facility for highly infectious pathogens "in a tornado-prone section of Kansas." Among other concerns, the GAO cites DHS's "flawed and outdated methodology" in its criticism. Those concerns are: "the ability of DHS and the federal government in general to safely operate a biosafety facility such as the proposed NBAF; the potential for a pathogenic release through accidents, natural phenomena, and terrorist actions; our May 2008 testimony that concluded that DHS had not conducted or commissioned a study to determine whether FMD research could be conducted safely on the U.S. mainland; natural phenomena such as tornadoes, earthquakes, and hurricanes that could cause catastrophic damage to the NBAF and result in the release of a pathogen; the possibility that an infected mosquito vector could escape, allowing a pathogen such as Rift Valley Fever virus to become permanently established in the United States; the economic effects of a release or a perceived release on the local, state, and national livestock industry."
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Meet Homeland Security's New Bioterror Czarina

Postby American Dream » Mon Aug 24, 2009 12:07 pm

http://antifascist-calling.blogspot.com ... -meet.html

A "Dark Winter" for Public Health: Meet Homeland Security's New Bioterror Czarina


In the wake of the 2001 anthrax attacks, successive U.S. administrations have pumped some $57 billion across 11 federal agencies and departments into what is euphemistically called "biodefense."

Never mind that the deadly weaponized pathogen employed in the attacks didn't originate in some desolate Afghan cave or secret underground bunker controlled by Saddam.

And never mind that the principal cheerleaders for expanding state-funded programs are Pentagon bioweaponeers, private corporations and a shadowy nexus of biosecurity apparatchiks who stand to make a bundle under current and future federal initiatives.

Leading the charge for increased funding is the Alliance for Biosecurity, a collaborative venture between the Center for Biosecurity of the University of Pittsburgh Medical Center (UPMC) and Big Pharma.

Speaking at the World Economic Forum in Davos, Switzerland in January 2005, former U.S. Senate Majority Leader William Frist, a Bushist acolyte, baldly stated that "The greatest existential threat we have in the world today is biological" and predicted that "an inevitable bioterror attack" would come "at some time in the next 10 years."

Later that year, Frist and former House Speaker Dennis Hastert (R-IL) covertly inserted language into the 2006 Defense Appropriations bill (H.R. 2863) that granted legal immunity to vaccine manufacturers, even in cases of willful misconduct. It was signed into law by President Bush.

According to Public Citizen and The New York Times, Frist and Hastert benefited financially from their actions; the pair, as well as 41 other congressmen and senators owned as much as $16 million in pharmaceutical stock. SourceWatch revealed that "the Biotechnology Industry Organization (BIO) is purported to be the key author of the language additions. This trade association represents virtually all major vaccine manufacturers."

The Senate Majority Leader's alarmist jeremiad at Davos was seconded by Dr. Tara O'Toole who added, "This [bioterrorism] is one of the most pressing problems we have on the planet today."

Really? Not grinding poverty, global warming or the lack of access by hundreds of millions of impoverished workers and farmers to clean water, an adequate diet, health care or relief from epidemic levels of preventable diseases such as malaria, tuberculosis or diarrhea, but "bioterrorism" as narrowly defined by securocrats and their academic accomplices.

But Dr. Victor W. Sidel, a founder of Physicians for Social Responsibility (PSR) and an outspoken critic of the Bioweapons-Industrial-Complex challenged O'Toole's hysterical paradigm.

Sidel made the point that there is a fundamental conflict between the state's national security goals and health care providers' professional responsibilities to patients. He wrote in 2003 that "military, intelligence, and law enforcement agencies and personnel have long histories of secrecy and deception that are contrary to the fundamental health principles of transparency and truthfulness. They may therefore be unsuitable partners for public health agencies that need to justify receiving the public's trust."

In this context, the choice of O'Toole as the Department of Homeland Security's (DHS) Undersecretary of Science and Technology is troubling to say the least. As former CEO and Director of UPMC's Center for Biosecurity, critics charge that O'Toole's appointment will be nothing short of a disaster.

No ordinary policy wonk with an impressive résumé and years as a government insider, O'Toole is a key player advocating for the expansion of dual-use biological weapons programs rebranded as biodefense.

Subverting the Biological Weapons Convention

The resuscitation of American bioweapons programs are facilitated by their secretive and highly-classified nature. Under cover of academic freedom or intellectual property rights, the U.S. Bioweapons-Industrial-Complex has largely been outsourced by the state to private companies and contractors at top American corporations and universities.

Efforts to strengthen the Biological Weapons Convention (BWC) by the inclusion of verification language into the treaty and regular inspection of suspect facilities by international experts have been shot-down since 2001 by the Bush and now, the Obama administrations. Why?

Primarily because the United States view onsite measures as a threat to the commercial proprietary information of multinational pharmaceutical and biotechnology companies as well as to America's reputedly "defensive" biological programs; initiatives that continue to work with nature's most dangerous and deadly pathogens.

In fact, the problem of the dual-use nature of such research is a conundrum facing critics who challenge the break-neck expansion of concealed weapons programs. Simply put, military activities can be disguised as commercial research to develop medical countermeasures without anyone, least of all the American people, being any the wiser.

Highly-trained microbiologists deployed across a spectrum of low-key companies, trained for academic, public health, or commercial employment are part of the dual-use problem. Who's to say whether scientists who genetically-manipulate pathogens or create Frankenstein-like chimera disease organisms (say, synthesized Marburg or Ebola virus as has already been done with poliovirus in a U.S. lab) are engaged in treaty-busting weapons research or the development of life-saving measures.

And what about the accidental, or more sinisterly, the deliberate release of some horrific new plague by a scientist who's "gone rogue"? As researcher Edward Hammond pointed out:

British researchers pled guilty in 2001 to charges that they improperly handled a genetically engineered hybrid of the viruses causing hepatitis C and dengue fever. British authorities characterized the virus as "more lethal than HIV". 'Dengatitis' was deliberately created by researchers who wanted to use fewer laboratory animals in a search for a vaccine for Hepatitis C. Under unsafe laboratory conditions, the researchers created and nearly accidentally released a new hybrid human disease whose effects, fortunately, remain unknown; but which may have displayed different symptoms than its parents and thus been difficult to diagnose, and have required a new, unknown treatment regime. (Emerging Technologies: Genetic Engineering and Biological Weapons, The Sunshine Project, Background Paper No. 12, November 2003)

A new report by the Center for Arms Control and Nonproliferation has charged that despite restrictions under the BWC prohibiting the development, production, stockpiling and use of weaponized disease agents such as anthrax, smallpox or plague, as well as equipment and delivery systems intended for offensive use, the rapid growth of "biodefense and research programs over the last decade" has placed "new pressure" on efforts to curb the development of banned weapons listed in the treaty.

In an interview with Global Security Newswire Gerald Epstein, a senior fellow with the hawkish Center for Security and International Studies (CSIS) told the publication, "When one is doing bioresearch and biodefense, one has to be careful to not overstep the treaty itself."

He cited the U.S biodefense effort Project Bacchus--an investigation by the Defense Threat Reduction Agency to determine whether it was possible to build a bioweapons production facility using readily available equipment--as an instance where questions were raised if the treaty had been violated.

The type of biodefense activity that is most likely to raise questions regarding treaty compliance is "threat assessment," the process of determining what type of biological attacks are most likely to occur, he told Global Security Newswire. A dangerous biological agent could inadvertently be developed during such research, Epstein said.
(Martin Matishak, "Biodefense Research Could Violate Weapons Convention, Report Warns," Global Security Newswire, August 20, 2009)

But Pentagon bioweaponeers did more than build "a bioweapons productions facility using readily available equipment." They built banned weapons. According to Jeanne Guillemin, author of Biological Weapons: From the Invention of State-Sponsored Programs to Contemporary Bioterrorism, the Pentagon and CIA made and tested a model of a Soviet anthrax bomb and created an antibiotic-resistant strain of anthrax.

After consulting with scientists who strongly suggested that the CIA anthrax bomb project would violate the BWC, "CIA lawyers decided the project was within the allowed realm of defensive research," Guillemin revealed. Project Clear Vision, a joint investigation by the CIA and the Battelle Memorial Institute, under contract to the Agency, reconstructed and tested a Soviet-era anthrax bomblet in order to test its dissemination characteristics. The Agency "decided the same" for the small, fully functional bioweapons facility built under the rubric of Project Bacchus.

The third initiative, Project Jefferson, led to the development of an antibiotic-resistant strain of anthrax based on a Soviet model. After the outgoing Clinton administration hesitated to give the CIA the go-ahead for the project, the Bush regime's National Security Council gave the Pentagon permission. "They believed" Guillemin wrote, "the Pentagon had the right to investigate genetically altered pathogens in the name of biodefense, 'to save American lives'."

Shortly thereafter, the Pentagon authorized the Defense Intelligence Agency (DIA), one of the most secretive and heavily-outsourced Defense Department branches, to re-create the deadly anthrax strain.

What the scope of these programs are today is currently unknown. We do know however, that based on available evidence the Department of Homeland Security, the Defense Department and the oxymoronic Intelligence Community, using the Department of Health and Human Services (HHS) and the U.S. Department of Agriculture (USDA) as a cover, continue to investigate the feasibility of transforming nature's most deadly pathogens into weapons.

In close coordination, the United States government and their outsourced corporate partners are spending billions of dollars on research and simulation exercises, dubbed "disaster drills" by a compliant media, to facilitate this grisly trade.

Secrecy and Deceit

That the official bioterror narrative is a preposterous fiction and swindle as even the FBI was forced to admit during its much-maligned Amerithrax investigation, is hardly worth a second glance by corporate media beholden to the pharmaceutical industry for advertising revenue; call it business as usual here in the heimat.

As we now know, the finely-milled anthrax powder which killed five people and shut down representative government didn't come from the Afghan-Arab database of disposable Western intelligence assets known as al Qaeda, but rather from deep within America's own Bioweapons-Industrial-Complex, to wit, from the U.S. Army Medical Research Institute of Infectious Diseases (USAMRIID) at Ft. Detrick in Maryland. But such troublesome and inconvenient truths are barely worth a mention by "respectable" media, e.g. the corporate stenographers who sold two imperialist military adventures to the American people.

Indeed, a credible case can be made that without the anthrax attacks, the fear levels gripping the country in the wake of the 9/11 terrorist events--and the subsequent clamp-down that followed, from the USA Patriot Act to the indefinite detention and torture of "terrorism" suspects, and from warrantless wiretapping to the demonization of dissent--may very well have been impossible.

It is difficult not to conclude that from the beginning of the affair, there was a clear intent on the part of the anthrax terrorist(s) to draw a straight line between 9/11 and the anthrax mailings. From there, it was but a short step to stitching-up a case for "regime change" in Iraq. The media's role in this criminal enterprise was indispensable for what Salon's Glenn Greenwald has called "the single greatest, unresolved media scandal of this decade." As Greenwald points out,

During the last week of October, 2001, ABC News, led by Brian Ross, continuously trumpeted the claim as their top news story that government tests conducted on the anthrax--tests conducted at Ft. Detrick--revealed that the anthrax sent to [former Senator Tom] Daschle contained the chemical additive known as bentonite. ABC News, including Peter Jennings, repeatedly claimed that the presence of bentonite in the anthrax was compelling evidence that Iraq was responsible for the attacks, since--as ABC variously claimed--bentonite "is a trademark of Iraqi leader Saddam Hussein's biological weapons program" and "only one country, Iraq, has used bentonite to produce biological weapons." (Glenn Greenwald, "Vital unresolved anthrax questions and ABC News," Salon, August 1, 2008)

Despite ABC News' claims that their information came from "four well-placed and separate sources," they were fed information that was patently false; as Greenwald avers, "No tests ever found or even suggested the presence of bentonite. The claim was just concocted from the start. It just never happened."

And as we will shortly explore below, the dubious "Dark Winter" and "Atlantic Storm" bioterror exercises designed by Dr. Tara O'Toole freely drew from the neocon's sinister playbook, right down to the weaponized smallpox supplied to al Qaeda by Saddam.

Whether or not one buys the current permutation of the "lone nut" theory, this one alleges that Dr. Bruce Ivins, a vaccine specialist employed by USAMRIID, was the anthrax mailer; the fact is, when all is said and done the attacks, to use a much over-hyped phrase, were an inside job.

And like other "lone nuts" who have entered the parapolitical frame at their own peril, Ivins isn't around to refute the charges.

The Alliance for Biosecurity: Insiders with a Mission and (Very) Deep Pockets

Before being pegged by the Obama administration to head DHS's Science and Technology division where she will oversee the department's billion dollar budget, with some 45 percent of it going towards chemical and bioweapons defense, O'Toole, as previously mentioned, was the CEO and Director of UPMC's Center for Biosecurity, a satrapy which describes itself as "an independent organization dedicated to improving the country's resilience to major biological threats."

How "independent"? You make the call!

According to their web site The Alliance for Biosecurity is "a collaboration among the Center for Biosecurity and 13 pharmaceutical and biotechnology companies whose mission is to work in the public interest to improve prevention and treatment of severe infectious diseases--particularly those diseases that present global security challenges."

Alliance partners include the usual suspects: Bavarian Nordic; Center for Biosecurity of UPMC; Cangene Corporation; DOR BioPharma, Inc.; DynPort Vaccine Company LLC, a CSC company; Elusys Therapeutics, Inc.; Emergent BioSolutions; Hematech, Inc., a subsidiary of Kyowa Kirin; Human Genome Sciences, Inc.; NanoViricides, Inc.; Pfizer Inc.; PharmAthene; Siga Technologies, Inc.; Unither Virology LLC, a subsidiary of United Therapeutics Corporation. Rounding out this rogues gallery are associate members, the spooky Battelle Medical Research and Evaluation Facility and the Lovelace Respiratory Research Institute.

Among the chief activities of the Alliance is lobbying Congress for increased funding for the development of new drugs deemed "countermeasures" under the Project BioShield Act of 2004, previously described by Antifascist Calling as a particularly grotesque piece of Bushist legislative flotsam.

The Alliance avers that "the United States faces unprecedented risks to national security ... by the clear and growing danger of bioterrorism or a destabilizing infectious disease pandemic," and that "our nation's vulnerability to biothreats is so severe" due to the fact that "most of the vaccines and medicines that will be needed to protect our citizens do not now exist." Therefore, countermeasures needed to mitigate nebulous biothreats never spelled out once in the group's literature "will likely require several years and several hundred million dollars each to successfully develop and produce." (emphasis added)

An Alliance report, The State of Biosecurity in 2008 and Proposals for a Public/Private Pathway Forward, charts a course for "improving and accelerating" efforts to "develop medical countermeasures (MCMs) for the nation's Strategic National Stockpile (SNS)."

Under the Project Bioshield Act of 2004, Congress authorized $5.6 billion over ten years "to purchase MCMs for the SNS." Funds were allocated for the procurement of the anthrax vaccine as well as for "therapeutic antibodies for inhalational anthrax, a botulism heptavalent antitoxin, a smallpox vaccine, and several products for radiological and nuclear threats, obligating a total of about $1.9 billion of the $5.6 billion BioShield fund."

In 2006 as I noted previously, Congress created the Biomedical Advanced Research and Development Authority (BARDA) within the Department of Health and Human Services (HHS). BARDA was authorized to spend some $1.07 billion over three years for MCMs, "only $201 million has been provided by Congress through FY 2008" noted the Alliance, "approximately one-fifth of the authorized level."

According to an "independent economic analysis" carried out by (who else!) the Alliance's academic partner, the Center for Biosecurity, "it would require $3.4 billion in FY 2009 to support one year of advanced development."

"Similarly" according to the organization, "the original appropriation of $5.6 billion for Project BioShield is equally insufficient to ensure that once MCMs are developed there will be funds available to procure them and maintain the stockpile." Indeed, "this level of funding would need to be sustained for many years." You can bet however, that Alliance lobbyists are busy as proverbial bees in pressuring Congress to fork over the dough!

The report state's that Alliance goals necessarily entail instilling "a sense of urgency ... with Congress" by hyping the "bioterror threat." But there's much more here than a simple cynical exercise at preparing the "public diplomacy" ground through academic and industry "message force multipliers" that will enable Congress to shower Big Pharma with a veritable tsunami of cash. A "risk-tolerant culture" should be promoted within BARDA, one that "understands the realities, risks, timelines, and costs of drug development."

The "risks" to whom and for what purpose are not enumerated, but one can be certain that a "risk-tolerant culture" crafted by industry insiders will come at the expense of the health and safety of the American people, one that pushes potential legal liability should things head south onto the taxpaying public.

The stealth nature of Alliance recommendations are clearly spelled out when they aver that "stakeholders" should "focus more on the potential biothreats and the corresponding countermeasures, rather than the price tag" and that BARDA, ostensibly a public agency, should be packed with insiders "who have drug development and manufacturing experience." This will lead to the development of "a culture that is focused on partnering with industry and academia."

But the bottom line as always, is the corporatist bottom line for Alliance shareholders! How else can one interpret their statement that emerging "biothreats" are all the more dire today now that "interest of the public and private capital markets in biodefense has declined over the last 2-3 years." What better way then, to beef-up those sagging capital markets than to install an industry-friendly individual at DHS with a documented track record of overplaying the "bioterror threat."

Dark Winter

O'Toole was the principal designer of two "tabletop" bioterror preparedness drills, the 2001 Dark Winter exercise and the 2005 Atlantic Storm run-through; both were criticized by scientific experts as fabrications of an alleged threat of a smallpox attack mounted by al Qaeda.

Reviewing Milton Leitenberg's 2005 report, Assessing the Biological Weapons and Bioterrorism Threat, published the U.S. Army War College's Strategic Studies Institute, protein chemist Dr. Eric Smith wrote the following:

Of note is Leitenberg's dissection of the process of assessment as practiced through bioterrorism threat scenarios conducted by the US government and private think tanks. Exercises like Dark Winter, which modeled an "aerosolized" smallpox attack, Top Off 2 and 3, both on pneumonic plague strikes, and Atlantic Storm, an exercise that purported to show an al Qaida group manufacturing a dry powder smallpox weapon, were rigged. In the cases of Dark Winter and the Top Offs, transmission rates of disease were sexed up beyond historical averages so that "a disastrous outcome was assured" no matter any steps taken to contain outbreaks. Eight pages are reserved to pointedly condemn the Atlantic Storm exercise on a host of sins which can generally be described as a bundle of frank lies and misinformation coupled with a claimed terrorist facility for making smallpox into a weapon that even state run biological warfare operations did not possess. And once again, juiced transmission rates of disease were employed to grease theoretical calamity. The reader comes to recognize the deus ex machina--a concoction or intervention added to dictate an outcome, in these cases very bad ones--as a regular feature of the exercises. However, the results of the same assessments--the alleged lessons learned--have never been reported with much, if any, skepticism in the media. (Eric Smith, "A Vaccine for the Hype: Milton Leitenberg's new 'Assessing the Biological Weapons and Bioterrorism Threat," Global Security, National Security Notes, March 31, 2006)

In criticizing "the fancy that such attacks are easy and one of the most catastrophic threats faced by the American people," Smith denounces the alarmist scenarios of Dark Winter and Atlantic Storm's designers--people like Dr. Tara O'Toole and the coterie of industry insiders and other well-paid "experts"--as guilty of perpetrating a massive "fraud ... and a substantial one" on the American people.

While one of Atlantic Storm's architects proclaimed "this is not science fiction" and that "the age of Bioterror is now..." Leitenberg and Smith denounce O'Toole's spurious claims as "not the least bit plausible."

Leitenberg wrote that "well before October-November 2001, the spectre of 'bioterrorism' benefitted from an extremely successful sales campaign." Indeed, hyped-up scenarios such as Dark Winter and Atlantic Storm that place "weapons of mass destruction" in the hands of shadowy, intelligence-linked terror outfits like al Qaeda provided "inflated predictions that ... were certainly not realistic. Much worse, in addition to being wrong, inflated predictions were counterproductive. They induced interest in BW in the wrong audiences."

But the implausible nature of the scenarios deployed in national exercises hardly prohibited the Bioweapons-Industrial-Complex from concocting scarecrow-like straw men designed to sow terror amongst the American people while extracting regular infusions of cash from Congress.

Among the eight exercises analyzed by Leitenberg between 1998-2005, he found that each and every one were fraudulently designed and the threat of bioterrorism had been framed as a rationalization for "political action, the expenditure of public funds for bioterrorism prevention and response programs," that could "not occur without it." This is "not benign," Leitenberg concludes.

A second consequence of sexed-up "bioterror" drills have even more ominous implications for the immediate future. Because of national security state perceptions that mitigation of catastrophic bioterrorism is of supreme importance for national survival--perceptions reinforced by academic, corporate and militarist peddlers of crisis--"the US biodefense research program appears to be drifting into violation" of the Biological Weapons Convention. This is a menacing development and has happened, I would argue precisely because the evaluation process which justifies research into biological weapons threat capabilities and scenarios, are repackaged to conceal the offensive thrust of this research as wholly defensive in nature, which it certainly is not.

How else would one explain ongoing research funded by the National Institutes of Health to study botulism toxin, "with the added qualification" Smith points out, that because the protein toxin is "unstable, therefore there will be collaboration with other researchers to stabilize it." The NIH grant "means preparing a much more effective botulinum toxin than had been available before."

Smith goes on to cite "another problematical breakout" offered by two scientists to study the "aerobiological" characteristics of the lethal Marburg and Ebola viruses. How this is "defensive" in nature, in keeping with research restrictions under the Biological Weapons Convention, is another instance of a backdoor move to kick-start illicit bioweapons development.

According to Smith, the study "looks to define how the organisms can be aerosolized, an instance of research into examining vulnerability in the complete absence of a verified threat." But I would argue that showering taxpayers dollars into such dark and troubling research tributaries deploy hyped-up threats as cover for the development of illegal weapons.

When her nomination was announced in May, Rutgers University and homeland security critic Richard Ebright told Wired,

"This is a disastrous nomination. O'Toole supported every flawed decision and counterproductive policy on biodefense, biosafety, and biosecurity during the Bush Administration. O'Toole is as out of touch with reality, and as paranoiac, as former Vice President Cheney. It would be hard to think of a person less well suited for the position."

"She was the single most extreme person, either in or out of government, advocating for a massive biodefense expansion and relaxation of provisions for safety and security," he adds. "She makes Dr. Strangelove look sane."
(Noah Shachtman, "DHS' New Geek Chief is a Bioterror 'Disaster,' Critics Charge," Wired, May 6, 2009)

And Dr. Smith told Wired that exercises designed by O'Toole and her colleagues show her to be "the top academic/salesperson for the coming of apocalyptic bioterrorism which has never quite arrived."

As noted above, "[She's] most prominent for always lobbying for more money for biodefense, conducting tabletop exercises on bioterrorism for easily overawed public officials, exercises tweaked to be horrifying," Smith told Wired.

But Smith goes even further and denounces O'Toole as an industry shill who "has never obviously appeared to examine what current terrorist capabilities have been... in favor of extrapolating how easy it would be to launch bioterror attacks if one had potentially unlimited resources and scientific know-how." It's a "superb appointment if you're in the biodefense industry and interested in further opportunity and growth."

"Alternatively" Smith avers, O'Toole's appointment is "a disaster if threat assessment and prevention" has "some basis in reality."

Not that any of this matters in Washington. The Senate Homeland Security and Governmental Affairs Committee led by "independent Democrat" and arch neocon Sen. Joseph Lieberman, voted to send her nomination to the full Senate July 29.
American Dream
 
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Postby American Dream » Sun Nov 15, 2009 7:37 pm

http://www.informationclearinghouse.inf ... e23969.htm

The Truth About The Anthrax Attacks

By Barry Kissin

I. INTRODUCTION – THE SMOKING GUN


November 15, 2009 "Truth Jihad" -- On September 16 and 17, 2008, the House and Senate Judiciary Committees respectively, conducted “Amerithrax oversight” hearings consisting of questioning FBI Director Robert Mueller. Despite widespread concern about the integrity of Amerithrax, the colloquy during these hearings was largely feeble. Congressman Nadler did manage to ask the $64,000 question. Salon.com journalist Glen Greenwald recounted this as follows:

“Nadler asked one of the most central questions in the anthrax case: he pointed out that the facilities that (unlike Ft. Detrick) actually have the equipment and personnel to prepare dry, silica-coated anthrax are the U.S. Army's Dugway Proving Ground and the Battelle Corporation, the private CIA contractor that conducts substantial research into highly complex strains of anthrax. Nadler asked how the FBI had eliminated those institutions as the culprits behind the attack. After invoking generalities to assure Nadler that the FBI had traced the anthrax back to Ivins' vial (which didn’t answer the question), Mueller's response was this: I don't know the answers to those questions as to how we eliminated Dugway and Battelle. I'll have to get back to you at some point.

“Nadler then pleaded: please try to get back to us with the answer quickly. Mueller replied: ‘Oh, absolutely Congressman.’”

Shortly thereafter, Nadler’s question was put into writing and sent to the FBI with other questions from the House Judiciary Committee. Nadler’s question read:

“How, on what basis, and using what evidence did the FBI conclude that none of the laboratories it investigated were in any way the sources of the powder used in the 2001 anthrax attacks, except the U.S. Army Laboratory at Fort Detrick, Maryland? Please include in your answer why laboratories that have publicly identified as having the equipment and personnel to make anthrax powder, such as the U.S. Army’s Dugway Proving Grounds in Dugway, Utah and the Battelle Memorial Institute in Jefferson, Ohio, were excluded as possible sources.”

Seven months went by before the FBI responded. Its response read:

“Initially, the spores contained in the envelopes could only be identified as Bacillus Anthracis (Anthrax). They were then sent to an expert, who “strain typed” the spores as Ames. Once the strain type was identified, the FBI began to look at what facilities had access to the Ames strain. At the same time, science experts began to develop the ability to identify morphological variances contained in the mailed anthrax. Over the next six years, new scientific developments allowed experts from the FBI Laboratory and other nationally recognized scientific experts to advance microbial science. This advancement allowed the FBI to positively link specific morphs found in the mailed anthrax to morphs in a single flask at USAMRIID. Using records associated with the flask, the FBI was able to track the transfer of sub samples from the flask located at USAMRIID to two other facilities. Using various methods, the FBI investigated the two facilities that received samples from the parent flask and eliminated individuals from those facilities as suspects because, even if a laboratory facility had the equipment and personnel to make anthrax powder, this powder would not match the spores in the mailed envelopes if that lab had never received a transfer of anthrax from the parent flask.” (Emphasis added).

On its face, the FBI’s response is absurd. The response literally says that after identifying “two facilities” that received samples of anthrax from the USAMRIID (Bruce Ivins’) flask, these facilities were excluded as possible sources of the attack anthrax because they “never received” anthrax from said flask.

One of the purposes of this memorandum is to make clear why Nadler’s question is the “most central” question to be asked about Amerithrax. This will serve to put in perspective Robert Mueller’s professed inability to answer the question on Sept. 16, 2008, the period of seven months it took for the FBI to fashion a response, and the disingenuousness of the response.

The FBI’s response is not only absurd; it is, to the extent it states anything at all, demonstrably false. Only a few months ago, Bruce Ivins’ “Reference Material Receipt Record” with respect to the anthrax designated RMR-1029 was posted on the internet, now accessible at http://caseclosedbylewweinstein.wordpre ... lask-1029/

The original copy of said record is in the custody of the FBI. Said record documents that during the summer of 2001, Bruce Ivins sent samples of RMR-1029 to both Battelle and Dugway. Practically all of the science underlying Amerithrax now being reviewed by the National Academy of Sciences is about matching the genetic fingerprint of the attack anthrax to that of RMR-1029. Given that both Battelle and Dugway had RMR-1029, Battelle and Dugway are no less incriminated than Bruce Ivins by the science underlying Amerithrax.

That the FBI has engaged in cover-up in its Amerithrax investigation is readily apparent. This memorandum addresses the urgent matter of what it is that is being covered up.

So far, Congress has failed in its oversight role with respect to Amerithrax. An important example of this failure is the absence of any reaction on the part of Congressman Nadler or any other member of Congress to the miserable FBI response highlighted in this Introduction.

II. BRIEF HISTORY RELEVANT TO THE ANTHRAX ATTACKS

At the Senate Judiciary Committee “Amerithrax oversight” hearing mentioned in the Introduction, Chairman Patrick Leahy (himself a target of one of the anthrax letters) made specific reference to an article entitled “U.S. Germ Warfare Research Pushes Treaty Limits” that appeared in the New York Times on September 4, 2001.

Excerpts from said article follow:

Over the past several years, the United States has embarked on a program of secret research on biological weapons that, some officials say, tests the limits of the global treaty banning such weapons . . .

“The projects, which have not been previously disclosed, were begun under President Clinton and have been embraced by the Bush administration, which intends to expand them.

“Earlier this year, administration officials said, the Pentagon drew up plans to engineer genetically a potentially more potent variant of the bacterium that causes anthrax, a deadly disease ideal for germ warfare . . .

“A senior Bush administration official said all the projects were 'fully consistent' with the treaty banning biological weapons and were needed to protect Americans against a growing danger. ‘This administration will pursue defenses against the full spectrum of biological threats,’ the official said . . .

“Some Clinton administration officials worried, however, that the project violated the pact. And others expressed concern that the experiments, if disclosed, might be misunderstood as a clandestine effort to resume work on a class of weapons that President Nixon had relinquished in 1969 . . .


[My comment: In 1975, it was discovered that the CIA had disobeyed the 1969 Presidential order to destroy all US BW stocks, and had retained a large catalogue of pathogens and toxins for its own use. Volume 1: Unauthorized Storage of Toxic Agents of the Church Committee Reports (1975) documented the unauthorized and illegal storage of toxic agents by the CIA for 5 years after their destruction was ordered by President Nixon. These toxins, stored at the Army’s Fort Detrick in Maryland, included anthrax and tuberculosis bacteria, the encephalitus virus, salmonella, shellfish toxin, the smallpox virus, and various other poisons and biological warfare agents.]

“Administration officials said the need to keep such projects secret was a significant reason behind President Bush's recent rejection of a draft agreement to strengthen the germ-weapons treaty, which has been signed by 143 nations . . .

[My comment: The “draft agreement” referred to was for a protocol that would provide for international inspections and verification measures, which agreement was supported by practically all of the other signatories to the international treaty known as the Biological Weapons Convention (BWC). In the past, the U.S. had repeatedly taken the position that enforceability of international arms control treaties depended on inspections and verification. The rejection by the Bush administration of inspections and verification (which has yet to be revisited by the Obama administration) was mirrored on October 23, 2002, when the UN Disarmament Committee adopted a resolution reaffirming the 1925 Geneva Protocol “prohibiting the use of poisonous gases and bacteriological methods of warfare.” The resolution passed unanimously with two abstentions: the U.S. and Israel. US abstention amounted to a veto, effectively preventing the resolution from being reported.]

“Among the facilities likely to be open to inspection under the draft agreement would [have been] the West Jefferson, Ohio, laboratory of the Battelle Memorial Institute, a military contractor that has been selected to create the genetically altered anthrax . . .

“Several officials who served in senior posts in the Clinton administration acknowledged that the secretive efforts were so poorly coordinated that even the White House was unaware of their full scope . . .

“[I]n 1997, the [CIA] embarked on [Project] Clear Vision, which focused on weapons systems that would deliver the germs . . . A model was constructed and the agency conducted two sets of tests at Battelle, the military contractor. The experiments measured dissemination characteristics and how the model performed under different atmospheric conditions, intelligence officials said . . .

“In the 1990's, government officials also grew increasingly worried about the possibility that scientists could use the widely available techniques of gene-splicing to create even more deadly weapons . . .

“Eventually the C.I.A. drew up plans . . . but intelligence officials said the agency hesitated because there was no specific report that an adversary was attempting to turn [an anthrax] superbug into a weapon.

“This year, officials said, the project was taken over by the Pentagon's intelligence arm, the Defense Intelligence Agency . . . Officials said the research would be part of Project Jefferson, yet another government effort to track the dangers posed by germ weapons.

“A spokesman for Defense Intelligence, Lt. Cmdr. James Brooks, declined comment. Asked about the precautions at Battelle, which is to create the enhanced anthrax, Commander Brooks said security was ‘entirely suitable for all work already conducted and planned for Project Jefferson.’”


At the end of this Sept. 4, 2001 New York Times article, it is stated that the article is based on material gathered for the about-to-be published book, Germs: Biological Weapons and America's Secret War.

Excerpts from Germs Biological Weapons and America's Secret War (2002: Touchstone, Simon & Schuster) follow:

“The CIA, [George Tenet] said, was looking for bold, imaginative solutions -- something that would 'break the back' of biological terrorism. . . . [T]he CIA and the Pentagon had been working separately for nearly three years on several highly classified projects to develop a better understanding of germ weapons and delivery systems . . . The programs were among the government's most closely held secrets, their code names known to only a handful of officials. . . . Officials privately acknowledged another reason for their sensitivity: the projects were bringing America much closer to the limits set by the 1972 treaty banning biological weapons. . . . [I]n the late 1980s, Senator John Glenn's investigation and hearing prompted much tighter limits on germ research. In the years that followed, scientists at Fort Detrick scrupulously confined their work . . . It was a different story at the CIA . . . A project took shape. CIA officials named it Clear Vision -- an attempt to see into the future of biological warfare . . . The [CIA] went ahead without asking the White House for approval . . . White House officials say that President Clinton was never told of the program . . . In the ensuing months, Battelle, a military contractor in Columbus, Ohio, with sophisticated laboratories, conducted at least two sets of tests . . . The program had become controversial, one senior intelligence official acknowledged, because 'it was pressing how far you go before you do something illegal or immoral.' . . . The State Department representative argued that the treaty ruled out any tests involving weapons. The CIA did not back down. Projects like Clear Vision, the agency argued, were a response to specific intelligence about a possible adversary. . . . By early 2001 . . . although some at the agency continued to defend the project's value, nevertheless, the program was out of money. . . . Senior Clinton officials had been briefed only on what a top official called 'one part of the iceberg that threatened to collide with the germ treaty.' (Pages 287-299).

“In the last days of the Clinton administration, the Pentagon gingerly moved toward doing its own recombinant work on pathogens. . . . To make the genetically modified anthrax, the DIA turned to Battelle, its contractor which had also worked on Clear Vision, the CIA project. . . . [This] secret project was to be done as part of Project Jefferson. (Pages 308-309).

“In fact, federal investigators found that the anthrax Daschle received was virtually indistinguishable from the kind William Patrick had made in the old U.S. program -- up to one trillion spores per gram . . . Fort Detrick had shipped a sample of its Ames strain to the Dugway Proving Grounds in the Utah desert, an army facility. Dugway subsequently made powdered anthrax . . . One year's experiments, the army said, did not involve the Ames strain. But it was silent on whether the potent variety had been used in other years.” (Pages 330-331).

[My comment: In 1999, William Patrick, the original inventor of anthrax weaponization, was commissioned to do an analysis of a hypothetical anthrax attack through the mail for the CIA. Ultimately, this classified document was leaked to the media. In his report entitled “Risk Assessment,” Patrick explained that 2.5 grams is the amount that can be placed into a standard envelope without detection. (The anthrax letters addressed to the Senators contained about 2 grams of anthrax.) In a footnote, Patrick noted that the U.S. had refined "weaponized" anthrax powder to the unprecedented extent of a trillion spores per gram. This degree of refinement corresponds with the extraordinary purity of the anthrax in the letters addressed to the Senators. According to a BBC program Newsnight that aired on March 14, 2002, accessible at http://news.bbc.co.uk/2/hi/audiovideo/p ... 873368.stm, both Patrick and the CIA denied the existence of this report.]

III. MAINSTREAM MEDIA REPORT THE TRUTH BEFORE
COVER-UP PREVAILS


Baltimore Sun, December 12, 2001

“Anthrax matches Army spores: Organisms made at a military laboratory in Utah are genetically identical to those mailed to members of Congress” by Scott Shane:

“For nearly a decade, U.S. Army scientists at Dugway Proving Ground in Utah have made small quantities of weapons-grade anthrax that is virtually identical to the powdery spores used in the mail attacks that have killed five people, government sources say. . . . Anthrax is also grown at the U.S. Army Medical Research Institute of Infectious Diseases at Fort Detrick . . . ut that medical program uses a wet aerosol fog of anthrax rather than the dry powder used in the attacks . . . Dugway's production of weapons-grade anthrax, which has never before been publicly revealed, is apparently the first by the U.S. government since President Richard M. Nixon ordered the U.S. offensive biowarfare program closed in 1969. Scientists familiar with the anthrax program at Dugway described it to The Sun on the condition that they not be named. . . .Scientists estimate that the letter sent to Senate Majority Leader Tom Daschle originally contained about 2 grams of anthrax, about one-sixteenth of an ounce, or the weight of a dime. But its extraordinary concentration - in the range of 1 trillion spores per gram - meant that the letter could have contained 200 million times the average dose necessary to kill a person. Dugway's weapons-grade anthrax has been milled to achieve a similar concentration, according to one person familiar with the program. The concentration exceeds that of weapons anthrax produced by the old U.S. offensive program or the Soviet biowarfare program, according to Dr. Richard O. Spertzel, who worked at Detrick for 18 years and later served as a United Nations bioweapons inspector in Iraq

. . . [M]any bioterrorism experts argue that the quality of the mailed anthrax is such that it could have been produced only in a weapons program or using information from such a program. . . .”


Washington Post, December 16, 2001.

“Capitol Hill Anthrax Matches Army's Stocks: 5 Labs Can Trace Spores to Ft. Detrick”

by Rick Weiss and Susan Schmidt:

“The FBI's investigation into the anthrax attacks is increasingly focusing on whether U.S. government bioweapons research programs, including one conducted by the CIA, may have been the source of deadly anthrax powder sent through the mail, according to sources with knowledge of the probe. The results of the genetic tests strengthen that possibility. The FBI is focusing on a contractor that worked with the CIA, one source said. . . .The scientists are still planning to do genetic testing on anthrax bacteria from the Defense Research Establishment Suffield, a Canadian military research facility, the University of New Mexico in Albuquerque, and the Battelle Memorial Institute in Columbus, Ohio, a government contractor doing research on anthrax vaccines. Those are the only other facilities [besides Dugway] known to have received samples from USAMRIID . . . The CIA's biowarfare program . . . involved the use of small amounts of Ames strain, an agency spokesman said yesterday. The CIA declined to say where its Ames strain material came from . . . Nevertheless, the FBI has turned its attention to learning more about the CIA's work with anthrax, which investigators were told about by the agency within the past few weeks, government officials said . . . The anthrax contained in the letters under investigation ‘absolutely did not’ come from CIA labs, the spokesman said . . . Law enforcement sources, however, said the FBI remains extremely interested in the CIA's work with anthrax, with one official calling it the best lead they have at this point. The sources said FBI investigators do not yet know much about the CIA program.”

Miami Herald (Knight Ridder), December 21, 2001

“Anthrax investigators focusing on strain from military facility” by David Kidwell:

“Federal anthrax researchers are attempting to match the strain that killed a Boca Raton man and four others to a weaponized strain secretly manufactured at a U.S. military facility in the Utah desert, according to sources familiar with the probe. Agents are examining lab workers and researchers who had access to the weaponized, powdered anthrax grown at the U.S. Army's Dugway Proving Grounds and later supplied to Battelle Memorial Institute, a military research company based in Columbus, Ohio . . . It is clear that a strong theory has emerged that the refined powder used in the anthrax attacks bears striking similarities to U.S. military grade anthrax manufactured only at Dugway . . .‘The anthrax at Dugway is the only known sample they intend to check right now. The investigation is clearly focused on the Dugway anthrax,’ said Dr. Ronald Atlas, dean of the University of Louisville Biology Department, and incoming president of the American Society of Microbiology. ‘The word in the scientific community is that they are very close to something.’ Homeland Security Director Tom Ridge said Thursday the FBI has ‘winnowed’ the field of its investigation . . .”

Nevertheless, on December 21, 2001 (the same day that the above-cited Miami Herald article was published), The Dispatch in Columbus, Ohio reported that FBI Director Robert Mueller had assured Ohio Republican Senator Mike DeWine that “no one with or formerly with Battelle is a suspect.”

To recapitulate, Battelle Memorial Institute (BMI) was not only doing the lab work in its own labs in West Jefferson, Ohio for the CIA’s weaponization project, it was also doing the lab work at the Army’s Dugway Proving Grounds in Utah for the DIA’s anthrax weaponization project.

Battelle has a “national security division” offering the services of a team of “engineers, chemists, microbiologists, and aerosol scientists supported by state-of-the-art laboratories to conduct research in the fields of bioaerosol science and technology.” On its Web site, Battelle called this research group “one-of-a-kind.” Battelle also makes one of the world’s most advanced medicinal powders. Battelle’s pharmaceutical division, BattellePharma, in Columbus, has developed electrostatically charged aerosols for inhalation. BattellePharma’s Web site boasted that the company’s new “electrohydrodynamic” aerosol “reliably delivers more than 80% of the drug to the lungs in a soft (isokinetic) cloud of uniformly sized particles.” Other powders, boasted the Web site, only achieve 20% or less.

[b]IV. THE COVER-UP


In order to cover-up the evident connection between our secret anthrax weaponization projects and the attack anthrax, it would be necessary to negate the fact that the attack anthrax (particularly in the letters to the Senators) was weaponized.

This aspect of the cover-up is described in “Anthrax Powder: State of the Art?” by Gary Matsumoto, that appeared in the November, 2003 edition (Vol 32) of Science Magazine:

“Early in the investigation, the consensus among biodefense specialists working for the government and the military [was that] . . . the powder mailed to the Senate . . . was a diabolical advance in biological weapons technology . . . In May 2002, 16 of these scientists and physicians published a paper in the Journal of the American Medical Association, describing the Senate anthrax powder as ‘weapons-grade’ and exceptional: ‘high spore concentration, uniform particle size, low electrostatic charge, treated to reduce clumping’ (JAMA, 1 May 2002, p. 2237) . . . [But] by the fall of 2002, the awe inspiring anthrax of the previous spring had morphed into something decidedly less fearsome. According to sources on Capitol Hill, FBI scientists now reported that there was ‘no additive’ in the Senate anthrax at all. . . . The reversal was so extreme that the former chief biological weapons inspector for the United Nations Special Commission, Richard Spertzel, found it hard to accept. ‘No silica, big particles, manual milling . . . That’s what they’re saying now, and that radically contradicts everything we were told during the first year of this investigation.’”

Of course, once the DOJ/FBI arrived at its formulation that Bruce Ivins was the lone culprit, it became that much more necessary to portray the attack anthrax as other than “weapons-grade.” Richard Spertzel, quoted in the above-cited Science Magazine, was not only a chief UNSCOM inspector, he also worked at Fort Detrick for 18 years, and served as Deputy Commander of USAMRIID. On August 5, 2008 (one week after the death of Bruce Ivins), the Wall Street Journal published an op-ed by Mr. Spertzel entitled “Bruce Ivins Wasn’t the Anthrax Culprit.” Excerpts follow:

“Let's start with the anthrax in the letters to Sens. Tom Daschle and Patrick Leahy. The spores could not have been produced at USAMRIID where Ivins worked, without many other people being aware of it. Furthermore, the equipment to make such a product does not exist at the Institute. Information released by the FBI over the past seven years indicates a product of exceptional quality. The product contained essentially pure spores. The particle size was 1.5 to 3 microns in diameter . . . What's more, they were also tailored to make them potentially more dangerous. According to a FBI news release from November 2001, the particles were coated by a ‘product not seen previously to be used in this fashion before.’ Apparently, the spores were coated with a polyglass which tightly bound hydrophilic silica to each particle. That's what was briefed (according to one of my former weapons inspectors at UNSCOM) by the FBI to the German Foreign Ministry at the time . . . The multiple disciplines and technologies required to make the anthrax in this case do not exist at USAMRIID. Inhalation studies are conducted at the Institute, but they are done using liquid preparations, not powdered products. The FBI spent between 12 and 18 months trying "to reverse engineer" (make a replica of) the anthrax in the letters sent to Messrs. Daschle and Leahy without success, according to FBI news releases.”

On August 18, 2008 (three weeks after the death of Bruce Ivins), FBI scientists and their consultants conducted a briefing for journalists with “well-respected scientific journals.” The transcription of the entire briefing accessible at http://docs.google.com/Doc?id=dc3wqmd7_33d2tjs5ct should be reviewed. The briefing is rife with evident evasions, contradictions and clumsy contrivances. Several excerpts (somewhat rearranged according to subject matter) follow:

BACKGROUND OFFICIAL: . . . Leading today's discussion is Dr. Vahid Majidi and Dr. Chris Hassell of the FBI. . . .

DR. MAJIDI: . . . After nearly seven years of investigation, we have developed a body of powerful evidence that allows us to conclude that we have identified the origin and the perpetrator of the 2001 Bacillus Anthracis mailing. . . .

“DR. MAJIDI: . . . We have obviously done a number of other analyses [of the attack anthrax], elemental characterization, that drove us to conclude that there were no additives.

BACKGROUND OFFICIAL: . . . [The silica] was on the inside of the spore and not on the outside of the spore. . . .

DR. MAJIDI: . . . That's what the whole concept or methodology of weaponization comes from, is to weaponize. That's really -- that's an ambiguous word, but what people mean by weaponize is that postproduction of the spores was silica added to it to make it more disbursable . . . So one last time. No additive was added to the sample to make it more disbursable.

. . . . So is the material being so easily dispersible really unusual? The answer is no.

DR. MICHAEL: The spore coat is a layer, as I understand it, that's within the spore and it's not the outermost layer of the spore. So the spore had sequestered silicon and oxygen in the same location on the spore coat. We found no additives; no exogenous material on the outside of the spores. We did have the opportunity to look at weaponized material to compare it to the letter material and they were very different. And the weaponized material the additives appear on the outside of the spore. Again, in the letter materials the silicon and oxygen were co-located on the spore coat, within the spore.

QUESTION: Did you develop any theories on where the silicon and oxygen came from, and do you think it played any role in making the spores super buoyant?

DR. MAJIDI: If I can actually pass that question to Dr. Burans, because he's our expert on processing.

DR. BURANS: In essence, as Dr. Michael described, the silicon associated with oxygen that was found within the spore, not on the surface of the spore, being present within the spore coat, which is covered by something called an exosporia, the silicon would not have contributed to the fluid-like qualities of the Anthrax powders.


[My comment: From where did Dr. Michael obtain his “weaponized material”? That question aside, additives on the outside of the exosporium is pre-1969 technology. The current technology involving polyglass made of tightly bound hydrophilic silica referred to by Richard Spertzel (see above) is located in the spore coat.]

QUESTION: And as to where it came from?

DR. BURANS: It's known that Bacilli are capable of mineralizing different types of elements including silicon, so as early as 1982 Bacilli species have been shown to localize silica within their spore coat.

QUESTION: Can I ask a follow-up?

DR. MAJIDI: It could have been within the growth media. It could have been within --

DR. BURANS: It was a natural occurrence.

DR. MAJIDI: -- natural occurrence, yes.

QUESTION: Can you tell us what the dry weight percentage was on the silicon and the oxygen?

BACKGROUND OFFICIAL: There was no exogenous silicon in the spores.

QUESTION: I appreciate that, but can you please tell me what the dry weight percentage was of the silicon?

BACKGROUND OFFICIAL: It was high.

QUESTION: It was high?

BACKGROUND OFFICIAL: Yes.


[My comment: The claim that spores could contain a “high” percentage of silicon as the result of a “natural occurrence” is absurd.]

QUESTION: But we still need to know the weight, because that tells you how this stuff was weaponized.

DR. MAJIDI: Just wait a second. Wait a second. You know, there is -- this -- I don't understand what -- you are using the term, “weaponized” -- no one -- when you look at weaponization, there is a clear definition. That is you have an anthrax spore; you do specific preparation to make it suitable for use as a biological weapon. The material that we recovered did not have any additives added to it to make it in any more easily dispersible. They material we have is pure spores . . .

DR. MAJIDI: So again, I don't want to get wrapped around the issue of how was a sample processed. The critical issue --

QUESTION: Isn't that part -- an important part of the evidence, though?

DR. MAJIDI: Well, no. The important part of the evidence is that the materials of the letter with the genetic mutations could exclusively be related only to RMR-1029. . . .

DR. MAJIDI: It would have been easy to make these samples at USAMRIID. . . .

BACKGROUND OFFICIAL: There is a misconception going around this room that very simple spore preparation, simply spores washed in water, when dried, are not dangerous and friable. That is a misconception. We have seen many biological preparations that when just washed with water and dried are extremely friable. . . .

QUESTION: Can you tell me in your preparations how long it took you to make a spore like this as of the SI enhancer or whatever -- the drying, et cetera? How long did that take?

DR. BURANS: Basically, it would take somewhere between three and seven days.

QUESTION: That's all? How many people did it take to do that to that; to --

DR. BURANS: One person can perform the operation. . . .

DR. MAJIDI: Those locations [from where RMR-1029 was submitted] -- it is not eight laboratories. I got to be clear about that. They came from different locations. A good number of them came from USAMRIID itself. And we're not disclosing the [other] location.

QUESTION: How many were outside of the United States, and how many were non-governmental labs?

DR. MAJIDI: None outside the United States.

QUESTION: Were they all government labs?

DR. MAJIDI: There's a fine distinction there and I don't know really what we call government and what we call quasi-governmental, so we're going just going to leave that as is. . . .

QUESTION: So I've seen different estimates. How many people at Detrick or anyone else actually have access to RMR-1029?

DR. MAJIDI: The total body -- the total universe of people at some point were associated with RMR-1029 -- I'll qualify that. Roughly, about 100-plus.

QUESTION: Hundred-plus. Were those all at Detrick, or other labs --

DR. MAJIDI: No, they were at Detrick and other labs.

QUESTION: Can you just tell us, of the eight samples that the letters matched to, how many places were they at? You were sort of vague earlier.

DR. MAJIDI: Sure. Let's just say they're definitely not at eight places.

QUESTION: But can you just give us the number? Why can't you give us the number?

DR. MAJIDI: Because if I provide you with the exact number -- well, there's a number of reasons, I'll just give you a generic one. We don't want you to bug those laboratories.

QUESTION: Well, don't give us the names, just tell us how many.

[Laughter.]

QUESTION: You've already told us a hundred people; right? So --

DR. MAJIDI: Yeah.

QUESTION: -- how many labs?

DR. MAJIDI: Hmm --

QUESTION: Is it one?

DR. MAJIDI: It's more than one.

[Laughter.]

DR. MAJIDI: Hmm --

QUESTION: Can we keep guessing?

[Laughter.]

QUESTION: Two?

QUESTION: Is it ten?

DR. MAJIDI: Okay, it's total two laboratories.

QUESTION: Total two. Including USAMRIID? Or --

BACKGROUND OFFICIAL: Two institutions.

DR. MAJIDI: Two institutions . . . that means USAMRIID and one other institution.


Of course, the other institution, the “quasi-governmental” lab, is Battelle. It bears pointing out that throughout the entire Amerithrax investigation, no one from either the FBI or the DOJ ever publicly mentions the name Battelle.

James Burans identified above as the FBI’s “expert on processing” is introduced at the beginning of the briefing by FBI Lab Director Hassell as “the associate laboratory director of the National Bioforensic Analysis Center.” Later in the briefing when Dr. Burans introduces himself, he says he is “from the U.S. Naval biodefense community,” that he “became a scientific consultant to the FBI in the early stages of the Anthrax investigation,” and that he “helped to establish the National Bioforensic Analysis Center . . . to support Homeland Security and the FBI.” What is never revealed is the fact that the Department of Homeland Security contracted with Battelle to manage and operate the National Bioforensic Analysis Center, and that James Burans is a Battelle employee.

One last excerpt from this briefing:

QUESTION: . . . you know, there are so many suspicions about the way [Amerithrax] has been handled.

DR. MAJIDI: I don't think, number one, we were ever going to put the suspicions to bed. There is always going to be a spore on the grassy knoll . . .


I will cite one other venue in which the FBI/DOJ Amerithrax cover-up has been promoted, namely, the New York Times. On January 4, 2009, the Times published on its front page an article by Scott Shane which Shane introduced as the product of “the deepest look so far at the [Amerithrax] investigation.” Excerpts follow:

“The Times review found that the F.B.I. had disproved the assertion, widespread among scientists who believe Dr. Ivins was innocent, that the anthrax might have come from military and intelligence research programs in Utah or Ohio. By 2004, secret scientific testing established that the mailed anthrax had been grown somewhere near Fort Detrick . . . By early 2004, F.B.I. scientists had discovered that out of 60 domestic and foreign water samples, only water from Frederick, Md., had the same chemical signature as the water used to grow the mailed anthrax.”

About two months later, this nonsense about water testing establishing that the attack anthrax was grown near Fort Detrick was retracted on the New York Times website as follows:

Postscript: February 28, 2009 (by Scott Shane)
A front-page article on Jan. 4 about Bruce E. Ivins, the late Army scientist who the Federal Bureau of Investigation says was responsible for the anthrax letter attacks of 2001, reported that F.B.I. scientists had concluded in 2004 that out of 60 domestic and foreign water samples, only water from near Fort Detrick, Md., where Dr. Ivins worked, had the same chemical signature as the water that had been used to grow the mailed anthrax. That information, provided by a former senior law enforcement official who did not want to be named in the article, suggested that the anthrax could not have come from military and intelligence research programs in Utah and Ohio, as some defenders of Dr. Ivins’s innocence had speculated. . . .


On Tuesday at an American Society for Microbiology conference in Baltimore, an F.B.I. scientist, Jason D. Bannan, said the water research ultimately was inconclusive about where the anthrax was grown. An F.B.I. spokeswoman, Ann Todd, said on Wednesday that the bureau ‘stands by the statements’ of Dr. Bannan.”

The author of this memorandum had something to do with this retraction being made. I composed a detailed critique of the N.Y. Times article, and Dr. Meryl Nass decided to post it on her website. I also attended the American Society for Microbiology conference in Baltimore referred to in the retraction, and was the individual who asked FBI scientist Bannan to comment about the “water research.” My critique is accessible at http://anthraxvaccine.blogspot.com/2009 ... ature.html

Another passage in this same New York Times article that warrants retractions is as follows:

“Though a public debate had raged for years over whether the mailed anthrax had been ‘weaponized’ with sophisticated chemical additives, the F.B.I. had concluded early on that it was not. Dr. Ezzell agreed, as did Jeff Mohr, an expert on anthrax and other pathogens at the Army’s Dugway Proving Ground in Utah. Without giving an opinion of Dr. Ivins’s guilt or innocence, both Dr. Ezzell and Dr. Mohr said they believed that any experienced microbiologist could have grown and dried the anthrax using equipment Dr. Ivins had in his laboratory.”

Previous statements by Drs. Mohr and Ezzell contradicted the view attributed to them in the N.Y. Times article. Dr. Mohr was interviewed for a recently released documentary entitled Anthrax War, (which documentary was co-produced by Congressman Nadler’s brother, Eric Nadler). In the documentary, Dr. Mohr is heard to plainly say that Dugway weaponizes anthrax. He also openly reveals that “a bunch of” scientists at Dugway worked with the FBI on Amerithrax, thus learned the “ins and outs” with respect to the characteristics of the attack anthrax, that the particles of attack anthrax were in the range of 1 micron in size, that size is only “one of the reasons it was so dangerous,” but that he has to be careful about what he reveals, because he (and the other Dugway scientists) signed statements promising not to talk about what the attack anthrax looked like.

Dr. Ezzell gave his original account of the attack anthrax to Marilyn Thompson, which account was reported in her book, The Killer Strain (HarperCollins: 2003):

“The FBI called Ezzell on October 15 [2001] to alert him that evidence would be brought from the Daschle crime scene straight to USAMRIID for testing. . . . [A]s Ezzell worked, he noticed a bit of white powder tucked into one of the letter's folds. Almost as soon as he saw it, the powder dispersed, spreading invisibly through the safety cabinet. After years of researching anthrax, he had never seen the bacteria in its weaponized form -- . . . a material that could blanket a city or annihilate an enemy. This was a powder so virulent that normal laboratory rules did not apply. Both he and his team could be at risk despite their precautions. . . . 'After all these years of looking, here it is. This is the real thing, in the right form,' he recalled. . . . To protect himself, Ezzell started antibiotics to guard against infection. He also took another precaution. Ezzell went to a sink and mixed a solution of diluted bleach. Bracing himself, he lifted it to his nose and took a deep snort. The pain that surged through his sinuses almost knocked him to the ground . . . Later in one of the regular interagency conference calls, Ezzell described what he had seen when he looked into the Daschle letter. He used the term weaponized anthrax. That night a friend who worked for the CIA woke him from a deep sleep to tell him that his assessment of 'weaponized' anthrax in the Daschle letter had been passed on to the President of the United States.” (Pages 116-118).

There is one other book that reports observations of the attack anthrax made during the first examinations of the Daschle anthrax. The Demon in the Freezer by Richard Preston (Oct. 2002, Random House) also reveals the seeds of the cover-up:

“October 16, 2001

On the morning of the 16th, the day after it was delivered to USAMRIID, the powder in the letter mailed to Senator Daschle was being studied by John Ezzell, the civilian microbiologist who accepted it from the agents of the FBI’s Hazardous Materials Response Unit [HMRU]. But, Jahrling wanted Tom Geisbert to get the sample under an electron microscope… [Geisbert] shoved it into one of the electron microscopes, a transmission scope, which is eight feet tall. The scope cost a quarter-million dollars. Geisbert sat down at the eye pieces and focused. The view was wall-to-wall anthrax spores. . . .The material seemed to be absolutely pure spores. . . [USAMRMC Chief] General Parker and Peter Jahrling went by the office of the USAMRIID Commander, Colonel Ed Eitzen, then the three men went upstairs to the scope room, where Tom Geisbert was staring at the anthrax. ‘It’s okay, I used to run an electron microscopy lab,’ Parker said. Parker sat down at the scope and looked. Pure spores. That was all he needed to see. He went out into the hallway and started issuing instructions to Eitzen and Jahrling in a rapid fire way: ‘We’re going to put USAMRIID into emergency operations . . .’

“October 17, 2001

. . . Major General John Parker went to the US Senate, where he met with a caucus of the Senate leadership and their staff. He told them that he looked at the anthrax himself in the microscope and that it was essentially pure spores. He would later say, ‘The letter was a missile …’ The FBI decided, sensibly, to get a second opinion on the Daschle anthrax. The HMRU dispatched a Huey to Fort Detrick…The helicopter took off with the sample and thupped westward over Maryland. It touched down in West Jefferson, Ohio near Columbus at the Hazardous Materials Research Center of the Batelle Memorial Institute. Batelle scientists took the [sample] into the lab. . . . Their tests showed that the anthrax was not nearly as refined or powerful as the Army people believed.

“October 18, 2001

. . . [During an Interagency Conference Call with individuals from National Security Council, FBI, CDC, and Army], Peter Jahrling replied that USAMRIID’s data indicated that the Daschle anthrax was ten times more concentrated and potent than any form of anthrax that had been made by the old American bio-warfare program at Fort Detrick in the 1960s. He said that the anthrax consisted of pure spores, and that it was ‘highly aerogenic’ . . . The spores of anthrax went straight through the paper of the Daschle envelope and other anthrax envelopes full of ultra-fine powder that were mailed, though they had been sealed tightly with tape.

“October 19, 2001

. . . Before dawn on Friday morning, four days after the Daschle letter was opened, Peter Jahrling put on a space suit and went into the Submarine and got a tiny sample of live, dry Daschle anthrax. He gave the sample to Tom Geisbert so that he could look at the dry anthrax in a scanning electron microscope. Geisbert carried the tube of dry anthrax into his microscope lab . . . [Geisbert] stared at the bone-colored particles. Now he saw them climbing the wall of the tube, dancing along the wall of the tube heading upward. His assistant, Denise Braun, was working near by. ‘Denise, you’ll never believe this.’ The anthrax was like jumping beans; it seemed to have a life of its own. He began preparing a sample for the scope. He opened the tube and tapped a little bit of the anthrax onto a piece of sticky black tape that would hold the powder in place. But the anthrax bounced off the tape. The particles wouldn’t stick. Eighty percent of the Daschle particles flittered away in air currents up into the hood. That was when he understood that the Hart Building was utterly contaminated . . . [Geisbert] had a national-security clearance, and he knew something about anthrax, but he could not imagine how this weapon had been made. It looked extremely sinister. He started feeling shaky. He called Jahrling. ‘Pete, I’m in the scope room. Can you come up here, like right now?’ Jahrling ran upstairs, closed the door, and stared at the skull anthrax for a long time. He didn’t say much. Geisbert’s security clearance was rated secret, and the details of how this material could have been made might be more highly classified. Not long afterward, Jahrling apparently went to the Secure Room and had the classified safe opened. He studied a document or documents with red-slashed borders that would appear to contain exact technical formulas for various kinds of weapons-grade anthrax. … Jahrling refers to the secret of scull anthrax as the Anthrax Trick although he won’t discuss it . . . [Geisbert] was afraid that his findings about the skull quality of the anthrax meant that it had come from a military biowarfare lab . . . Meanwhile in Washington , the FBI laboratory was trying to evaluate the anthrax. On the same day that the two Brentwood workers died, a meeting was held at FBI headquarters involving the FBI laboratory, scientists from the Battelle Memorial Institute and scientists from the Army. Battelle and the Army people were doing what scientists do best; disagreeing totally with one another. The Army scientists were telling the FBI that the powder was extremely refined and dangerous. While a Battelle scientist named Michael Kuhlman was allegedly saying that the anthrax was ten to fifty times less potent than the Army was claiming . . . The Department of Health and Human Services was not getting briefed about the anthrax to its satisfaction by the FBI. An HHS official who was close to the situation but who did not want her name used had this to say about the Battelle analysis of the Daschle anthrax: ‘It was one of the most screwed-up situations I’ve ever heard of. The people at Battelle took the anthrax and heated it in an autoclave, and this caused the material to clump up, and then they told the FBI it looked like puppy chow. It was like a used- car dealer offering a car for sale that’s been in an accident and is covered with dents, and the dealer is trying to claim this is the way the car looked when it was new.’

“October 24, 2001

Early in the morning, nine days after the Daschle letter was opened, Major General John Parker got a call from Tommy Thompson at Health and Human Services. Thompson had been hearing rumors that the Daschle anthrax was really bad stuff, but he still hadn’t heard much about it from the FBI laboratory . . . [At the White House, that evening:] John Ashcroft led off the meeting. He didn’t mince words. There was an obvious lack of communication between the Army, the FBI, and the CDC, he said, and the purpose of this meeting was to determine why the CDC hadn’t realized that the anthrax was weapons--grade material and hadn’t taken action faster on the Brentwood mail facility . . . Ashcroft was Robert Mueller’s boss and he looked straight at the FBI director. Mueller turned his gaze to General Parker. Mueller thanked the Army for bringing the nature of the anthrax to the FBI’s attention. He said that the FBI had received conflicting data on the anthrax. The FBI had been trying to sort this issue through, but Mueller now acknowledged that the Army had been right: the Daschle anthrax was a weapon.

“October 25, 2001

Tom Geisbert drove his beat-up station wagon to the Armed Forces Institute of Pathology, in northwest Washington, carrying a whiff of sterilized dry Daschle anthrax mounted in special cassette. He spent the day with a group of technicians running tests with an X-ray machine to find out if the powder contained any metals or elements. By lunchtime, the machine had shown that there were two extra elements in the spores, silicone and oxygen. Silicone oxide. Silicone dioxide is glass . . . The glass was slippery and smooth, and it may have been treated so that it would repel water. It caused the spores to crumble apart, to pass more easily through the holes in the envelopes, and fly everywhere, filling the Hart Senate Office Building and the Brentwood and Hamilton mail-sorting facilities like a gas.”


(Pages 200-234).

“One day, I [author Richard Preston] spoke with a scientist who is an expert in forensic evidence, knows a lot about biology, and until recently was an influential executive in the FBI. ‘We just don’t know who these perpetrators are, and it could be years before we get a break. I’m saying ‘they.’ I personally find it hard to believe it was done by only one person . . . If I wanted to keep tight operational security…I would do it with opsec. Opsec—operational security. It’s a standard security approach for making yourself as invisible as possible. There is a leader who organizes and directs an operation, and a different person carries it out.’ The person who does the operation is expendable.”

(Pages 246-247).

V. CONCLUSION

In 1961, in his “Farewell Address,” President Eisenhower warned of the emerging power of the “military-industrial complex.” In the ensuing almost fifty years, that warning has gone unheeded, and we have been engaged in what Gore Vidal calls “perpetual war.” Our military and so-called “national security” expenditures exceed the total of what the entire rest of the world spends.

We by far export more weapons than any other country. We maintain at least 750 military bases around the world. We are what Martin Luther King called the “greatest purveyor of violence in the world.” So much of what we now do in the name of national security (including our wars in Iraq and Afghanistan) actually undermines our security, not only by multiplying our enemies, bankrupting our treasury, and instigating international arms races, but by perpetuating massive delusion.

The insanity of our course is exemplified in the system surrounding the anthrax letters of 2001. This, the only bio-attack in our history, is an officially acknowledged “inside job,” one that we know originated from our own so-called “biodefense” program. No, the anthrax letters were not the work of a “lone nut.” They were the work of our military-industrial-intelligence complex, a complex of revolving participants that manufactures weapons and war for power and profits.

The decision in early 2001 to unilaterally reject inspections and verification as a part of international bioweapons arms control (precisely to avoid inspections of our secret weaponization projects) was the choice to pursue arms race over arms control. The anthrax letters that soon followed served and fulfilled two purposes. As a “false flag operation,” with language in the letters that read “Death to America, Death to Israel, Allah is Great,” the anthrax attacks played a major role in the run-up to the Iraq war. As a stimulator of fear of bio-threat, the anthrax attacks served as the pretext for a massive expansion of our so-called biodefense program, with expenditures on this program quickly becoming twenty times what they were before the attacks.

I am a longtime resident of Frederick, Maryland, home of Fort Detrick. Fort Detrick has been headquarters for our biowarfare/biodefense programs ever since their inception in 1943. The plan is to make Detrick the site of a National Inter-agency Biodefense Campus (NIBC). Construction of two of the NIBC’s facilities is already completed, one an NIH facility called the Integrated Research Facility (IRF), the other a Homeland Security (DHS) facility called the National Biodefense Analysis and Countermeasures Center (NBACC). Both NIH and DHS have already entered into contracts worth $750 million with the same private company for the management and operation of these facilities – the name of that company is Battelle. DHS is also entrusted with constructing the National Bio and Agro-Defense Facility (NBAF), a 500,000 square foot facility, which will have within its walls more BSL-4 laboratory space than three times the total amount of BSL-4 space in the entire country as of 2004. All indications are that DHS will be contracting with Battelle to manage and operate this facility as well.

Just the week before this memorandum is being submitted, there were three separate Congressional committees conducting hearings about the massive proliferation of high-security bio-laboratories being built across the country. In the first such hearings that took place back in October, 2007, Keith Rhodes of the GAO testified: “High-risk labs have health risks for individual lab workers as well as the surrounding community . . . [E]ven labs within sophisticated biological research programs, including those most extensively regulated, have had and will continue to have safety failures." Only massive delusion can explain how in all of these hearings, no one except the GAO is seriously questioning the need for, the rationale behind this proliferation. The multitude of government-sponsored advisory panels, like the National Research Council committee that just issued a 161-page report, practically all appear to begin with the assumption that this proliferation is essential to national security. Only massive delusion can explain how we could assume that the necessary response to the only bioattack in our history is to massively expand the program that itself generated that attack.

The operation of our military-industrial-intelligence complex is impervious to changes in Federal administration. Though the anthrax attacks and the design of the new “biodefense” program happened under the Bush administration, the Obama administration’s appointment of Tara O’Toole as the head of DHS’s Science and Technology division illustrates the nature of our system. Tara O’Toole was the CEO and Director of the University of Pittsburgh’s Center for Biosecurity, which describes itself as “an independent organization dedicated to improving the country’s resilience to major biological threats.”

According to their web site, The Alliance for Biosecurity is “a collaboration among the Center for Biosecurity and 13 pharmaceutical and biotechnology companies whose mission is to work in the public interest to improve prevention and treatment of severe infectious diseases -- particularly those diseases that present global security challenges.” Alliance partners include Emergent BioSolutions (manufacturer of the only vaccine licensed by the FDA for the prevention of anthrax infection), Human Genome Sciences, Inc. (that recently received a $1.8 billion contract to help the government stockpile anti-anthrax antibodies, whose directors include Richard Danzig, former Secretary of the Navy and a national security advisor to President Obama), and Battelle.

O’Toole was the principal designer of two bioterror preparedness drills, the 2001 “Dark Winter” exercise and the 2005 “Atlantic Storm” drill. According to a U.S. Army War College’s Strategic Studies Institute publication by Milton Leitenburg, these drills were based on a bundle of lies and misinformation including a claimed terrorist capability of making a bio-weapon that state-run programs do not possess, and exaggerated transmission rates of disease employed to exaggerate the resultant calamity. The drills were fraudulently designed so as to frame the threat of bioterrorism as a rationalization for the increased expenditure of public funds.

Well-respected Professor Richard Ebright of Rutgers University stated: “Tara O’Toole supported every flawed decision and counterproductive policy on biodefense, biosafety, and biosecurity during the Bush Administration . . . She was the single most extreme person, either in or out of government, advocating for a massive biodefense expansion and relaxation of provisions for safety and security.”

Respectfully submitted on October 2, 2009,

____________________________

Barry J.C. Kissin, Esq. - barrykissin@hotmail.com
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Postby Hugo Farnsworth » Mon Nov 16, 2009 11:15 am

A BSL-4 facility in Galvestion???????????

WTF?

MSM said nothing about this during Ike.

http://www.semp.us/publications/biot_reader.php?BiotID=544

It doesn't appear to have been handled all that well, and Ike was a relatively small, weak storm (Cat 2).
Without traversing the edges, the center is unknowable.
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Postby American Dream » Tue Dec 01, 2009 9:59 pm

http://antifascist-calling.blogspot.com ... ricas.html

Public Menace-Private Profit: America's Biowarfare Alliance


In September, The New York Times reported that a University of Chicago researcher, Malcolm Casadaban, died after exposure to "a weakened and ordinarily harmless strain of the bacteria that cause plague."

According to the Times, "Dr. Casadaban, an associate professor at the university, was studying the bacteria to create a better vaccine for plague ... in part because of concerns about its possible use in bioterrorism." The Times averred that "infectious disease experts said researchers rarely die from being infected with an ordinarily harmless strain of the bacteria or viruses they are studying."

Which of course, raise inevitable and troubling questions: just how "safe" was the strain of plague studied by Casadaban, and was this research part of a new round of illicit, highly compartmented experiments meant to bulk-up America's first-strike arsenals?

While there is no evidence that Casadaban ever worked on banned weapons, indeed the molecular geneticist was a leading expert into the origins of bubonic plague, the casual agent responsible for the Black Death, and an opponent of biological warfare, what of his colleagues?

One expert, Dr. Kenneth Alexander, told the Times "there might have been something unusual about the bacteria that caused it to be dangerous, a mutation, for example." Alexander hastened to add that "it was more likely" that the researcher had a "pre-existing condition," one that "made him more susceptible to infection."

Perhaps. But according to Edmond Hammond, director of the now-defunct Sunshine Project, records pried from the federal government through the Freedom of Information Act uncovered a disturbing pattern of criminal neglect amongst university and corporate officials.

Hammond discovered, and shared with Congress back in 2007, information that should have blown the lid off of one of America's dirtiest--and deadliest--little secrets. In excruciating detail, citing case after case, Hammond told congressional investigators that amongst the deadly pathogens that escaped containment in a series of underreported accidents were the following substances: Plague, anthrax, Rocky Mountain spotted fever, tularemia, brucellosis and Q fever.

Lab workers became sick, communities were threatened and yet, illicit work with these dangerous germs continue; just another day at the office for militarists, corporate grifters and their academic accomplices.

While Dr. Casadaban's death is a tragedy for family and friends, was a "pre-existing condition" responsible for the scientist's demise or was something more sinister taking place behind closed doors without his knowledge?

In the former Soviet Union, the Sunshine Project revealed that scientists involved in illegal offensive biowarfare research developed "plague bacteria (Yersinia pestis) ... that were resistant to 16 different antibiotics. Today, the genetic introduction of antibiotic resistance into bacterial pathogens is routine work in almost any microbiology laboratory."

While it is quite possible that Casadaban's death was a freak accident, nothing however can, or should, be ruled out.

Fanciful speculation? Better think again!

In June, Global Security Newswire reported that during a routine inventory at the U.S. Army Medical Research Institute of Infectious Diseases (USAMRIID) at Fort Detrick, Md., safety officers "found nearly 10,000 more vials of potentially lethal pathogens than were known to be stored at the site."

Claiming that there are "multiple layers of security," Ft. Detrick's deputy commander Col. Mark Kortepeter said it was "extremely unlikely" that any of the center's samples had been smuggled out. "Unlikely," but not impossible.

Amongst the 9,200 extra samples uncovered during the inventory were "bacterial agents that cause plague, anthrax and tularemia; Venezuelan, Eastern and Western equine encephalitis viruses; Rift valley fever virus; Junin virus; Ebola virus; and botulinum neurotoxins." In other words substances which can, and probably have, been weaponized by the Pentagon.

As Antifascist Calling previously reported, with "biodefense" as a cover, the U.S. National Security State has spent tens of billions of dollars ($56.9 billion since 2001, according to the Center for Arms Control and Non-Proliferation) on secretive programs investigating the deadliest pathogens known to nature, or ginning up new chimeric monsters in any number of privately-run labs.

The antinuclear watchdog group Tri-Valley CAREs (TVC) obtained documents under the Freedom of Information Act that revealed how Lawrence Livermore National Laboratory (LLNL), a "limited liability corporation" overseen by the University of California, Bechtel, BWX Technologies, Washington Group International and Battelle, routinely violated federal regulations and had carried out "restricted experiments" that resulted in the inadvertent release of anthrax in 2005.

Noting that "the relevant details of the 2005 anthrax accident were kept from the public at the time, just as happened with the illegal experiments that are coming to light today," TVC learned that this work is expanding, with little in the way of effective oversight by Congress or indeed, by any regulatory agency.

LLNL has now opened a Biosafety Level 3 (BSL-3) facility and is planning to experiment with pathogens exquisitely suited for use as offensive weapons. Activities contemplated include, "aerosolizing (spraying) pathogens such as plague, tularemia and Q fever, in addition to anthrax. Moreover, government documents disclose that planned experiments in the BSL-3 include genetic modification and potentially novel manipulation of viruses, prions and other agents."

In October, TVC filed a motion for summary judgement in Federal Court in the Northern District of California "aiming to stop the operation of a bio-warfare agent research facility at the Lawrence Livermore National Lab (LLNL) main site in Livermore, California."

According to TVC, "the large inventory of multiple bio-weapon agents, the presence of genetically modified variants, and the fact that some of the pathogens have been put into just the right form to be effectively spread via an airborne release, all serve to make the Livermore BSL-3 a potential magnet for terrorism from either an internal or external source."

Currently, some 400 research facilities and more than 15,000 individuals are cleared "to have access to select agents, which include anthrax, smallpox and the Ebola virus," according to a September report by the National Research Council.

The NRC averred that lax security at laboratories that work with select agents "pose a severe risk to human or animal health," risks that "have grown as the amount of research has increased in recent years."

And if one or more of these researchers should "go rogue," for money or as a plausibly deniable component of a Pentagon or CIA operation, doesn't the public have the right to expect the civilian side of government would weed out such miscreants from work with these deadly toxins?

A History of Illicit Research

The close proximity of U.S. biological warfare programs and the pharmaceutical industry is hardly an historical accident. From its inception, American research drew from a rich pool of biomedical researchers backed by the formidable technological resources of Big Pharma.

As Leonard Cole revealed in his 1988 exposé, Clouds of Secrecy: The Army's Germ Warfare Tests over Populated Areas, biowarfare research during World War II and the Cold War period was a public/private affair in which the government provided funds to state agencies and private corporations alike in the hope that such solicitous relationships would lead to breakthroughs in the area of offensive weapons or what is now euphemistically called "biodefense."

Indeed, none other than George W. Merck, the president of the Merck Pharmaceutical Company, was a top-flight consultant to the Secretary of War. In that capacity, Merck and his company provided expertise and technological know-how for work on America's nascent biowar programs. In a 1946 report to the Secretary of War penned by Merck, Cole revealed that the program "included research, testing, development, and production of biological agents," all carried out as Merck wrote, in the "strictest secrecy."

While wartime fears of biological attacks by the Axis powers represented a clear and present danger to the United States and their allies as revelations of Nazi Germany and Imperial Japan's active programs attest, this information was scrupulously covered-up and suppressed for decades. Indeed after the war, the United States actively recruited these sociopaths into their biological, chemical and nuclear weapons programs.

As is now known, America's military establishment struck a devil's bargain with the same war criminals who, in the name of science, visited death upon millions. While the doctors and biologists who filled the ranks of Japan's Unit 731 hadn't achieved a "breakthrough" in terms of delivery systems' development, as researcher Sheldon H. Harris revealed in Factories of Death, they possessed an invaluable resource sought by U.S. bioweaponeers: detailed records of the Japanese Army's obscene human experiments.

After the war with a new official enemy looming on the horizon--the Soviet Union--Merck admonished the state to maintain a strong biological warfare program, writing: "Work in this field, born of the necessity of war, cannot be ignored in time of peace; it must be continued on a sufficient scale to provide an adequate defense."

By 1948, the newly-emerging national security state stood-up a Committee on Biological Warfare within the Department of Defense to do just that. Shortly thereafter, the Central Intelligence Agency, particularly the Company's Technical Services Division (TSD), so-called "wizards of Langley," ran a series of illicit programs that sought to "secure the realm" through the application of the latest advances in the biological and psychological sciences.

Over decades, projects such as Bluebird, Artichoke, MKDELTA, MKNAOMI and MKULTRA, variously identified by researchers as "mind control" projects--which they were--garnered outrage when it was revealed during the 1970s that the Agency conspired with leading psychiatrists, psychologists, medical doctors, biologists and academic institutions in funding obscene human experiments employing psychoactive drugs such as LSD, mescaline and BZ on unwitting test subjects.

As the Senate Select Committee on Intelligence Activities, popularly known as the Church Committee, revealed during hearings to examine the Watergate scandals of the 1970s, the Pentagon's own programs ran simultaneously with those of the CIA. The Committee discovered:

In many respects, the Army's testing programs duplicated research which had already been conducted by the CIA. They certainly involved the risks inherent in the early phases of drug testing. In the Army's tests, as with those of the CIA, individual rights were also subordinated to national security considerations; informed consent and followup examinations of subjects were neglected in efforts to maintain the secrecy of the tests. Finally, the command and control problems which were apparent in the CIA's programs are paralleled by a lack of clear authorization and supervision in the Army's programs. (Senate Select Committee on Intelligence Activities, Project MKULTRA, The CIA's Program of Research in Behavioral Modification, United States Senate, August 3, 1977, Appendix A, p. 92)

While these projects may only have achieved modest success in standing up programmable assassins, as evidence on Lee Harvey Oswald and Sirhan Sirhan may suggest, MKULTRA and its spin-offs were primarily behavioral modification programs subsequently useful for what are now euphemistically termed "enhanced interrogation techniques," e.g., torture and as a formidable bioweapons project.

Indeed, Ft. Detrick's Special Operations Division (SOD), chock-a-block with CIA officers and assets, was, by the early 1950s experimenting with, and assembling biologically-based assassination weapons that were easily concealed and could be deployed by "wet work" specialists to murder foreign leaders such as the multiple failed plots against Fidel Castro, or Patrice Lumumba attest. As researcher Ed Regis documented, Congolese Prime Minister Lumumba was a thorn in the secret state's side.

Refusing to play ball with Washington so as to facilitate the extraction of that nation's vast mineral wealth by American multinational corporations, Lumumba sealed his fate when he sought military assistance from the Soviet Union. At that point, the national liberation leader became an object for Agency "executive action."

It was around this time that the CIA's Deputy Director for Plans, Richard Bissell, had a couple of informal talks with his scientific adviser, Sid Gottlieb, concerning the subject of the covert assassination of foreign leaders. Gottlieb suggested that biological agents were perfect for the task: they were invisible, untraceable, and, if intelligently selected and delivered, not even liable to create a suspicion of foul play. The target would get sick and die exactly as if he'd been attacked by a natural outbreak of an endemic disease. Plenty of lethal or incapacitating germs were out there and available, Gottlieb told Bissell, and they were easily accessible to the CIA. (Ed Regis, The Biology of Doom, New York: Henry Holt and Company, 1999, pp. 182-183)

While proponents of continued research with nature's deadliest pathogens argue that the Biological Weapons Convention (BWC) allows for purely "defensive" work to protect the public against potential bioattacks, this mendacious logic studiously avoids the issue of the dual-use nature of this work.

Cole unearthed documents, including a 1968 official history of Ft. Detrick penned by a Pentagon bioweaponeer who asserted forthrightly that "research and development in the offensive aspects of BW proceeded hand in hand with defensive developments for, in truth, the two are almost inseparable."

But MKULTRA and its grisly spin-offs are a thing of the past, right? Not by a long shot!

Jeffrey Kaye, a psychologist and critic of the torture-enabling American Psychological Association (APA), revealed November 23, that the group had organized a workshop in 2007 at the Arlington, Virginia headquarters of the dodgy RAND Corporation.

That conference, entitled "Science of Deception: Integration of Practice and Theory," discussed new and novel ways "to utilize drugs and sensory bombardment techniques to break down interrogatees. Those are signal techniques of psychological torture long utilized by the CIA and other intelligence agencies and military around the world."

Citing APA documents, Kaye discovered that APA and their friends at CIA were actively looking for "pharmacological agents ... known to affect apparent truth-telling behavior." Kaye learned that amongst the probative questions driving the spooks and contractors was this revealing sentence: "What are sensory overloads on the maintenance of deceptive behaviors? How might we overload the system or overwhelm the senses and see how it affects deceptive behaviors?"

According to numerous researchers, the CIA, and the psychologists and psychiatrists they contracted to work with them, including many of the top behavioral scientists of their day, experimented with many drugs in their quest to find a “truth” drug that would open up the recalcitrant and expose the liar and the dissembler. The CIA has declassified a paper from its in-house intelligence journal from the early 1960s, "'Truth' Drugs in Interrogation," where they discuss research on drugs for interrogation ranging from scopolamine, amphetamines, and barbiturates to cannabis, LSD, and mescaline. The CIA authors discuss the limitations of using drugs, based on research, and conclude that a special use for drugs may be found in detection of deception. (Jeffrey Kaye, "Who Will Investigate CIA/RAND/APA Torture 'Workshop'?," The Public Record, November 21, 2009)

What was true throughout the Cold War period is just as true today and remains a pressing public health issue. As Global Security Newswire reported in August, the U.S. Army Medical Research Institute of Infectious Diseases (USAMRIID) began construction on a new facility at Ft. Detrick in Frederick, Maryland. The brief report states that "new site will allow for more study of lethal diseases and should have space for 952 staffers, compared to the 800 now using facilities that date back four to five decades."

While the National Academy of Sciences "plans to assess health and safety issues raised by observers who believe there has been insufficient consideration regarding the potential release of an infectious agent from the facility," the same can also be said for the BSL-3 and BSL-4 facilities in private hands, under contract to the U.S. government.

As I reported in "Bringing the (Bio) War Home," the Bulletin of the Atomic Scientists revealed that "massive U.S. biodefense spending and a buildup of high-containment laboratories throughout the country might have created an internal security risk that no outside terrorist group could ever duplicate. Nearly two dozen new federal and many more new private biosafety level 3 and 4 laboratories have been built in recent years, meaning a large cadre of scientists has access to extraordinarily lethal material."

And if today's bioweaponeers have their way, such risks will increase exponentially with untold consequences for us all.

Building Banned Weapons

Leading experts, as I reported in August, have derided the possibility that terrorist groups have the know-how to fabricate smallpox or other pathogens into biological weapons as a massive "fraud ... and a substantial one" perpetrated on the American people.

Hysterical claims by securocrats that "bioterrorism is one of the most pressing problems we have on the planet today," an assertion made by Dr. Tara O'Toole, the Undersecretary of Science and Technology at the Department of Homeland Security, is not borne out by the facts.

Indeed, such claims not only distort available evidence that terrorist groups have such capabilities but conceal the more salient fact that Pentagon weaponeers continue to build banned weapons.

According to Jeanne Guillemin, author of Biological Weapons: From the Invention of State-Sponsored Programs to Contemporary Bioterrorism, the Pentagon and CIA made and tested a model of a Soviet anthrax bomb and created an antibiotic-resistant strain of anthrax.

After consulting with scientists who strongly suggested that the CIA anthrax bomb project would violate the BWC, "CIA lawyers decided the project was within the allowed realm of defensive research," Guillemin revealed.

Project Clear Vision, a joint investigation by the CIA and the Battelle Memorial Institute, under contract to the Agency, reconstructed and tested a Soviet-era anthrax bomblet in order to test its dissemination characteristics. The Agency "decided the same" for the small, fully functional bioweapons facility built under the rubric of Project Bacchus.

The third initiative, Project Jefferson, led to the development of an antibiotic-resistant strain of anthrax based on a Soviet model. After the outgoing Clinton administration hesitated to give the CIA the go-ahead for the project, the Bush regime's National Security Council gave the Pentagon permission. "They believed" Guillemin wrote, "the Pentagon had the right to investigate genetically altered pathogens in the name of biodefense, 'to save American lives'."

Shortly thereafter, the Pentagon authorized the Defense Intelligence Agency (DIA), one of the most secretive and heavily-outsourced Defense Department branches, to re-create the deadly anthrax strain.

Commenting on the close proximity of the 2001 anthrax provocation and the rush towards the invasion and occupation of Iraq, constitutional law expert Glenn Greenwald writes that the anthrax attack "played at least as large of a role as the 9/11 attack itself, if not larger, in creating the general climate of fear that prevailed for years in the U.S. and specifically how the anthrax episode was exploited by leading media and political figures to gin up intense hostility towards Iraq."

Which is why, according to Greenwald, "it's so striking how we've collectively flushed this terrorist attack down the memory hole as though it doesn't exist." Indeed, "what makes this particularly significant is that the anthrax attack is unresolved and uninvestigated."

Here we have one of the most consequential political events of the last decade at least--a lethal biological terrorist attack aimed at key U.S. Senators and media figures, which even the FBI claims originated from a U.S. military lab. The then-British Ambassador to the U.S. is now testifying what has long been clear: that this episode played a huge role in enabling the attack on Iraq. Even our leading mainstream, establishment-serving media outlets--and countless bio-weapons experts--believe that we do not have real answers about who perpetrated this attack and how. And there is little apparent interest in investigating in order to find out. Evidently, this is just another one of those things that we'll relegate to "the irrelevant past," and therefore deem it unworthy of attention from our future-gazing, always-distracted minds. (Glenn Greenwald, "A key British official reminds us of the forgotten anthrax attack," Salon, November 27, 2009)

On and on it goes, America's headlong rush into the abyss.

While the American people believed the election of Barack Obama signaled a change in direction from decades' long policies that have brought the planet to the brink of disaster, those hopes are little more than cynical illusions manufactured by media specialists and spin-doctors, the ubiquitous army of "message force multipliers" who do the bidding of their corporatist masters.

After all, $57 billion buys much in the way of silence.
American Dream
 
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Postby American Dream » Sat Dec 19, 2009 5:09 pm

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SATURDAY, DECEMBER 19, 2009

Letting the Beast Out of the (Corporatist) Bottle: Obama Channels Bush on Bioweapons


The Obama administration's recent declaration on bioweapons would simply be another run-of-the-mill example of our "change" president's duplicity were it not such an unmitigated disaster.

Recapitulating sinister Cold War practices that informed American ruling class consensus when it came to secretly toying with nature's most deadly pathogens, (a) because they could, (b) because it was, and is, highly profitable and (c) because they got with it, the profound failure by the administration to rein-in out-of-control corporate grifters, militarists and scientists thirsting after an endless flow of taxpayer dollars, have put us all on a potential glide path towards the abyss.

Since the roll-out of the Obama product-line January 21, on issues ranging from war and peace to economic justice and from civil liberties to healthcare, the "change" team exhibit the same callous disregard for disarmament proposals that characterized their Bushist predecessors in the Oval Office.

Nowhere is this reality so transparently delineated than by the administration's continuing efforts to derail plans to revitalize the moribund Biological Weapons Convention (BWC), rejecting binding verification protocols that would finally give the 1972 treaty teeth.

"Strengthening" the BWC: Killing it with Kindness

From her perch as U.S. Undersecretary of State for Arms Control and International Security, Ellen Tauscher, a former Democratic congresswoman from the San Francisco Bay Area (in other words, a feckless "liberal" who spent her career paying lip-service to the antiwar sentiments of her constituents--and then voting in favor of every blood-soaked imperialist adventure undertaken by the Bush regime) rejected international monitoring of military and pharmaceutical sites that might employ research for illicit purposes, e.g., the fabrication of banned biological weapons.

"The Obama administration will not seek to revive negotiations on a verification protocol to the convention," Tauscher told delegates December 9 at the annual meeting of the States Parties to the Biological Weapons Convention in Geneva.

The position outlined last week by the administration eerily follows in the footsteps of the previous government. In 2001, there was broad support internationally for revitalizing the BWC draft Protocol; a long, circuitous process undertaken back in 1991.

But during these earlier negotiations, the U.S. Pharmaceutical Research and Manufacturers of America (PhRMA) released a position paper opposing the routine inspection of laboratories and other research facilities on the grounds of safeguarding "confidential business information," a position they have reiterated today.

This, along with U.S. Defense Department opposition killed the deal after the American delegation, under instructions from arch neocon John Bolton who then held Tauscher's brief, argued that an international inspections regime would put U.S. "national security" at "risk" by allowing spot checks of suspected U.S. weapons sites.

Revealing a warmer and fuzzier, though no less obstructionist side than blustery Bolton, the Undersecretary mounted a charm offensive in Geneva, touting the National Security Council's (NSC) "National Strategy for Countering Biological Threats" as a major transformation of the U.S. position. It wasn't. Tauscher told delegates: "The United States intends to implement this [NSC] strategy through renewed cooperation and more thorough consultations with our international counterparts in order to prevent the misuse and abuse of science while working together to strengthen health security around the world."

However, not a single word in the 23-page NSC document addresses the vital issue of verification. Indeed, while no-holds-barred inspections of nuclear weapons' facilities undergird international treaties governing the destruction of warheads and missiles, thus ensuring compliance with treaty obligations by states, when it comes to biological weapons the "National Strategy" skirts the question entirely. Why?

While the United States claims that it will "advance policies and practices that establish and reinforce norms against the misuse of the knowledge and capabilities that arise from the life sciences while encouraging their free and open availability for peaceful and beneficial use," a call to "develop and employ complementary and multi-layered systems for influencing, identifying, inhibiting, and interdicting biological threats" does nothing to constrain state or corporate actors from exploiting the life sciences for nefarious ends, to wit, work with dual use select agents that can be diverted into surreptitious weapons' programs.

This is crucial. While the document asserts that America's "relationships with the United Nations, international organizations, foreign governments, and the private sector are critical to the success of our efforts" the fact is, the "private sector" and the secret state's own Defense Department are dead-set against any initiative that give international arms' control monitors access to their facilities.

Claiming that the United States "has carefully reviewed previous efforts to develop a verification protocol," the administration has "determined that a legally binding protocol would not achieve meaningful verification or greater security."

Echoing Tauscher and the NSC's lame reasoning, Barry Kellman, president of the International Security and Biopolicy Institute told The Hill he "agreed," and told the publication "that given the rapid evolution of the biological market, technologies that once could only be made in a laboratory can now be made anywhere, so it would be impossible to verify that a country is holding true to the convention protocols."

Really? Perhaps then, Mr. Kellman would care to enlighten us as to which select agent was used in the first and to date, only, bioterrorist attack of the 21st century, and where pray tell it might have come from.

Editing Out the Secret State: The 2001 Anthrax Attacks

As has generally been accepted by scientific experts and as The Baltimore Sun revealed back in 2001, "for nearly a decade, U.S. Army scientists at Dugway Proving Ground in Utah have made small quantities of weapons-grade anthrax that is virtually identical to the powdery spores used in the [October 2001] mail attacks."

Investigative journalist Scott Shane disclosed that Dugway's Life Sciences Division "made hundreds of kilograms of anthrax for bombs designed to kill enemy troops over hundreds of square miles" during the Cold War.

Indeed, the "extraordinary concentration" of the finely-milled powdered anthrax mailed to the media and members of Congress was "in the range of 1 trillion spores per gram" which "meant that the letter could have contained 200 million times the average dose necessary to kill a person."

Researchers at Northern Arizona University determined that "the genetic fingerprint of the mailed anthrax is indistinguishable from that of the Ames 'reference strain,' which is the strain used most often at Fort Detrick and Dugway, according to a scientist familiar with the genetic work," the Sun reported.

Years later, former Ft. Detrick deputy commander Richard Spertzel told investigative journalists Bob Coen and Eric Nadler that "the material that was in the Daschle/Leahy letter was "1.5 to 3 microns in particle size" and characterized the refinement "as super sophisticated ... phenomenal." When investigators attempted to examine samples under a microscope, "it readily floated off the slides."

In other words, the "genetic fingerprint" and "extraordinary concentration" of the weaponized anthrax used in the attack would require a team of individuals, and not a proverbial "lone nut" to produce a biotoxin possessing such exquisitely lethal characteristics. The inescapable conclusion is that the anthrax used to murder five people, sicken dozens of others and terrorize the rest of us, could only have come from a state program or one operating under contract to a government agency.

Could the deadly biotoxin have been diverted from a U.S. defense facility or corporate lab by a group of "black box" scientists operating under the radar for their own nefarious ends, i.e. strengthening the state's repressive hand within the social-political context of the 9/11 attacks? It is certainly possible and cannot be ruled out.

As I previously reported, Global Security Newswire (GSN) disclosed in June that "a recently completed inventory at a major U.S. Army biodefense facility found nearly 10,000 more vials of potentially lethal pathogens than were known to be stored at the [Ft. Detrick] site."

According to reporter Martin Matishak, the 9,220 samples discovered "included the bacterial agents that cause plague, anthrax and tularemia; Venezuelan, Eastern and Western equine encephalitis viruses; Rift valley fever virus; Junin virus; Ebola virus; and botulinum neurotoxins."

While Ft. Detrick's deputy commander Col. Mark Kortepeter claimed there are "multiple layers of security" and that "a lot of buffers [would] prevent anyone who shouldn't be in the laboratory from getting in in the first place and then preventing them taking something out with them," this dodges the question of whether someone who was authorized to be inside Ft. Detrick or any of the other 400 U.S. facilities that have Biosafety Level-3 or Biosafety Level-4 laboratories, could smuggle out deadly toxic substances.

The New York Times reported December 9, that Tauscher rejects a strict regulatory regimen that would monitor state bioweapons research and development because of the "regulatory burdens that verification would place on the American pharmaceutical industry and on the military's bio-defense research activities."

Given the available facts surrounding the 2001 anthrax terrorist incident and the FBI's subsequent cover-up, Tauscher's fear of "regulatory burdens" on the "pharmaceutical industry" and the state's own "bio-defense research activities" are certainly misplaced and should be viewed with suspicion.

Big Pharma and Congress: Best Friends Forever!

While journalists and researchers have explored ethically-challenged relationships amongst former Defense Department officials and the weapons' industry, most recently by USA Today, and have described the oft-cited revolving door as entrée to an exclusive and highly lucrative good 'ol boys club; call it a Beltway version of a retirement village for Pentagon clock-punchers.

Inquiring minds can't help but wonder: does the same clubby atmosphere pervade, and inform, the policy decisions made by denizens of the Bioweapons-Industrial-Complex? Let's take a look!

Take the Alliance for Biosecurity, a Big Pharma lobby shop aligned with the Center for Biosecurity of the University of Pittsburgh Medical Center (UPMC), as a starting point. Self-described as "a collaboration among the Center for Biosecurity and 13 pharmaceutical and biotechnology companies," one "whose mission is to work in the public interest to improve prevention and treatment of severe infectious diseases--particularly those diseases that present global security challenges," one discovers that similar relationships between academia, industry and government abound.

Since Antifascist Calling first reported on Alliance efforts to increase state funding of biotechnology and "biodefense" research in August, all references to the Alliance for Biosecurity have been scrubbed from UPMC's web site. Indeed, all traces of the lobby shop's activities, including group policy statements and testimony before relevant congressional committees have simply vanished.

But why, pray tell, would they take evasive action in the first place? And more importantly, what do they have to hide? As it turns out, quite a lot.

According to The Washington Times, when the Center for Biosecurity's director, Dr. Tara O'Toole, was nominated for her current post as Undersecretary of Science and Technology at the Department of Homeland Security, she had "served as a key adviser for a lobbying group funded by the pharmaceutical industry that has asked the government to spend more money for anthrax vaccines and biodefense research."

Reporter Tim McElhatton disclosed that O'Toole "never reported her involvement with the lobbying group called the Alliance for Biosecurity in a recent government ethics filing." The Washington Times further reported that the Alliance "has spent more than $500,000 lobbying Congress and federal agencies--including Homeland Security--since 2005, congressional records show."

"In written testimony to Congress" according to McElhatton, "Dr. O'Toole said the alliance was 'created to protect the Center for Biosecurity's status as an honest broker between the biopharma companies and the U.S. government'." As is well known, $500,000 buys much in the way of "honesty" in the halls of Congress!

In an October 31 letter to House Speaker Nancy Pelosi (D-CA) "signed by Dr. O'Toole and two other alliance officials, the group called on Congress to include more than $900 million for the 'advanced development of medical countermeasures' to be administered by the Biomedical Advanced Research and Development Authority."

The Washington Times revealed that the letter was also "signed by the chief executive officer of member company PharmAthene, David Wright, who was one of the two first co-chairmen for the alliance after its creation in 2005."

McElhatton reported that according to a Securities and Exchange Commission filing "Mr. Wright's company has a big financial interest in securing work from the authority," and that "PharmAthene has been trying to win a contract administered by the authority to supply 25 million doses of an anthrax vaccine to the national stockpile."

According to a press release, the firm announced that PharmAthene "will participate in and present data at the HHS Public Health Emergency Medical Countermeasures Enterprise (PHEMCE) workshop and BARDA Industry Day taking place in Washington, DC Dec. 2-4, 2009."

Indeed, the PHEMCE work shop "will bring together public and private sector stakeholders for a dynamic dialogue on the current state of medical countermeasure preparedness, PHEMCE initiatives in the past year, and plans for moving forward to enhance national capabilities to respond to a public health emergency."

When "moving forward" entails the expenditure of nearly one billion dollars for "countermeasure preparedness," one can be sure that companies on the make will be all ears!

Former Bushist Secretary of Health and Human Services, Tommy Thompson, averred that the PHEMCE workshop "is very timely given the WMD Commission's conclusion that terrorists are much more likely to attack America with a biological weapon than a nuclear weapon."

Despite the fact that weapons' experts have not reached a consensus on the Commission's alarmist report, given the extreme difficulty faced by "terrorists" to fabricate biotoxins into an effective weapon, Thompson claims, "now that our national experts have made this warning clear, we need to take the immediate steps necessary to protect against potential biological attacks against the U.S. homeland. In particular, we need to move forward efforts to build and stockpile appropriate biological countermeasures, such as next-generation anthrax vaccines, recombinant influenza vaccines, and novel antivirals."

Among the "experts" consulted by the WMD Commission were none other than Dr. O'Toole's Center for Biosecurity who have called for the expenditure of some $3.4 billion annually on "countermeasure development to reach 90 percent chance of success defending the country against bioterrorism threats."

Nowhere however, in the PharmAthene press release is it disclosed that the former HHS Secretary has a proprietary interest in securing federal dollars allegedly to "enhance national capabilities" to better respond "to a public health emergency." Currently, Thompson is the President of Logistics Health, Inc., a firm that does extensive business with the U.S. Department of Defense for what it euphemistically calls "military readiness."

Craig Holman, the legislative director of the watchdog group Public Citizen, said that O'Toole's lack of transparency "definitely and clearly runs counter to the intent of the law."

What was the response by Senate Democrats, quick to denounce the "culture of corruption" of their coconspirators across the aisle? According to The New York Times, Senate Majority Leader Harry Reid "slammed Republicans for slowing down, and in some cases, blocking the confirmation of nominees for various posts in the Obama administration."

Neither Reid, nor for that matter the Times, breathed a word about O'Toole's obvious conflict of interest and cosy relationships with biodefense firms she would presumably oversee from her perch at DHS.

Instead, we are lavished with empty rhetoric from Reid who told the Times: "'For that position, [DHS Undersecretary] President Obama nominated an expert in combating both pandemics and bioterror attacks,' Mr. Reid said, adding: 'Imagine that: Americans are bracing against a flu epidemic here at home and threats of terrorism from abroad, the President nominated someone highly experienced in both of those areas, and Republicans are saying no'."

Despite revelations of serious ethical breaches, O'Toole was confirmed by the Senate November 4.

The Ties that Bind (And Pay Handsomely!)

The close proximity of O'Toole, the Center for Biosecurity and now, the Department of Homeland Security to Alliance members such as Bavarian Nordic; Cangene Corporation; DOR BioPharma, Inc.; DynPort Vaccine Company LLC; Elusys Therapeutics, Inc.; Emergent BioSolutions; Hematech, Inc.; Human Genome Sciences, Inc.; NanoViricides, Inc.; Pfizer Inc.; PharmAthene; Siga Technologies, Inc.; Unither Virology LLC, , as well as associate Alliance member, the spooky, CIA-connected Battelle Memorial Institute, might just help explain the Obama administration's opposition to strengthening the BWC.

According to the Center for Responsive Politic's OpenSecrets.org database, the Alliance for Biosecurity have contributed some $600,000 to congressional grifters since 2005 through the Philadelphia law firm Drinker, Biddle & Reath.

While chump change when it comes to assuring that the best congresspeople money can buy stay "on-message," OpenSecrets reports that since 1990, Big Pharma and their allies in the health products industry have spent a whopping $177,030,005 on "influence and lobbying." Breaking down the numbers, the watchdog group avers that the bulk of contributions have benefited Republicans ($111,405,078 or 63%) vs. Democrats ($65,056,643 or 37%).

In The Washington Times piece cited above, ethics groups have said that the Alliance's set-up "is an example of what critics call "stealth lobbying," in which like-minded companies form a loosely knit compact and spend lots of money lobbying the government. The arrangement is legal, but it exposes loopholes that prevent the public from finding out how much money each company pays and whether one business exerts more control over the others."

Alliance legal counsel Anita Cicero told the paper, "the group is complying with all applicable federal laws" and that the group "does not generate income, does not have a bank account and does not owe taxes." She told the paper the organization "was formed so companies, academic institutions and the government" could work together to "accelerate the development of therapeutic and vaccine countermeasures."

"Countermeasures" that markedly add to the corporatist bottom line.

As Antifascist Calling previously reported, the National Biodefense Science Board (NBSB), chock-a-block with industry insiders and academic shills, posted an August 11 notice buried in the Federal Register.

Rescued from oblivion by the whistleblowing intelligence and security web site Cryptome, we were informed that NBSB's "Market & Sustainability Work Group" seek to hand over even more cash to industry partners.

Seeking public comment on the group's working document, "Inventory of Issues Constraining or Enabling Industry Involvement in Medical Countermeasure Efforts," NBSB is seeking to further "streamline" the Food and Drug Administration's already lax review process in a move meant to further "incentivize" industry by "increased federal funding for advanced development, in the form of cost-reimbursement contracts and rewarding private-capital investments with milestone payments at procurement."

Under NBSB's proposal, the drug industry stands to grab "reimbursement of development costs + 15%, with return-on-working-capital at 22%, and cost-of-money-for-capital at 15%."

If said corporate patriots swing into action during a national emergency, then "compensation if commercial product(s) during emergencies (e.g., lost sales, market share, delayed licensing" are fully paid by the federal government. Talk about a robust "public-private partnership" in action!

But wait, there's more!

GSN reported in October that Alliance member Human Genome Sciences Inc. had earned $160 million from the federal government for sales of its ABthrax vaccine, despite a Food and Drug Administration report that stated although the product performed better than a placebo (!) "it is still unknown how well these models and results predict efficacy in humans." Despite these equivocal findings, "Washington has placed an order for 65,000 doses of ABthrax for the country's emergency medicines reserve."

Now that's what I call a streamlined review process!

Earlier in October, GSN disclosed that Alliance member Emergent BioSolutions won $4.9 million in funding from the U.S. National Institute of Allergy and Infectious Diseases, a branch of the National Institutes of Health, "for the development of a new anthrax vaccine that could require only two doses to provide protection."

As investigative journalists and filmmakers Bob Coen and Eric Nadler revealed in Anthrax War and a companion book, Dead Silence: Fear and Terror on the Anthrax Trail, Emergent BioSolutions has a very interesting pedigree indeed.

When the State of Michigan auctioned off the Michigan Biological Products Institute (MBPI) in 1998, standing in the wings with a check for $24 million were Lebanese financiers Ibrahim El-Hibri and son Fuad, "an international telecom magnate" according to Coen and Nadler. During this period, the firm the El-Hibri's had founded after scooping-up MBPI for a song, BioPort, "held the exclusive contract to provide the U.S. government with the anthrax vaccine, and that in addition to the physical plant, the Michigan sale included $130 million in contracts with the Department of Defense."

During their investigation, Coen and Nadler learned "that the El-Hibris had participated in the privatization of portions of the United Kingdom's leading biodefense facility, Porton Down, a decade earlier" and that "with the acquisition of the Michigan plant, the family had planted stakes in the only two leading anthrax vaccine producers in the West." What makes this particularly troubling according to Coen and Nadler, is the fact that the "El-Hibri's did not have science backgrounds or biotech business experience before the Porton takeover--but were clearly canny investors."

Alarmingly, "the troubling fact [was] that the sale of MBPI to BioPort had transferred control of a sensitive government program to a network of companies, one of which was headquartered in the Dutch Caribbean."

Indeed, "Fuad El-Hibri himself informed Congress in 1999 that the controlling shareholder in BioPort--Intervac LLC--was partly owned by I and F Holdings NV, a Netherlands Antilles investment company owned by his father."

None of this troubled Congress in the least since, as Coen and Nadler relate "no one on the House Committee on Government Reform asked him if El-Hibri senior had any partners in I and F Holdings." These disturbing facts led the investigative journalists to wonder: "Who actually owned the largest anthrax vaccine manufacturing plant in the West, if not the world? Who really knew."

Fast forward a decade and according to GSN BioPort, now Emergent BioSolutions, "is the producer of BioThrax, the only vaccine licensed by the Food and Drug Administration for the prevention of anthrax disease. The company is also developing other anthrax treatments and countermeasures against diseases such as botulism and hepatitis B." Funds for developing the vaccine were provided "through the American Recovery and Reinvestment Act of 2009."

Last month, GSN revealed that Alliance member, Danish firm Bavarian Nordic will receive some $40 million for a freeze-dried version of the firm's Imvamune vaccine for smallpox. GSN reported that "Bavarian Nordic has received $680 million in contracts for Imvamune from the U.S. government. Washington has ordered 20 million doses of the vaccine in its liquid-frozen form and has the option of buying another 60 million," according to a company press release.

This, despite the fact that smallpox has disappeared as an international public health threat. However as the Sunshine Project's Edward Hammond revealed in Emerging Technologies: Genetic Engineering and Biological Weapons, when a U.S. research team at the State University of New York in Stony Brook synthesized poliovirus "from scratch," the responsible bioresearch community were alarmed.

Hammond commented that "the experiment exemplifies possibilities that generate real problems if similar techniques become applicable to agents such as smallpox. Today it is unlikely (though not completely impossible) that countries apart from Russia and the USA have access to smallpox virus. This is the basis of the current threat assessments with regard to smallpox, which rate the likelihood of a smallpox attack very low. Should it become possible in a few years to build smallpox virus in the laboratory, the situation would be turned upside down. The relative security that can be assumed today (at least for most countries in the world) will evaporate."

Since Hammond's piece first appeared in 2003, is it plausible that synthetic smallpox could have been ginned-up in a top secret U.S. research facility, hence contingency planning by secret state officials to have a freeze-dried, hence longer-lived vaccine on hand? We don't know.

Examining only the three above-named firms, OpenSecrets reports that since 2000, Human Genome Sciences has expended some $24 million since 2002 for lobbying; Emergent BioSolutions has spent some $10.9 on lobbying efforts since 2003, and Bavarian Nordic has spent some $21.7 lobbying Congress since 2002.

Given the enormous outlay of taxpayer largesse to firms that have profited handily under the Project BioShield Act of 2004, a grotesque piece of Bushist legislative flotsam, and the nearly $60 billion dollars reported by the Center for Arms Control and Non-Proliferation spent on so-called biodefense by the federal government, one can only conclude that lobbying activities by Big Pharma is an investment well-spent!

Keep in mind too, that the expenditure of federal dollars for Project BioShield and related programs do not include black budget allocations concealed by the CIA and Pentagon under a welter of above top secret Special Access Programs, a subject that Antifascist Calling will explore in future reports.

Conclusion

As the Sunshine Project's Edward Hammond has warned: "Rapid developments in biotechnology, genetics and genomics pose a variety of environmental, ethical, political, and social questions. And because they open up tremendous new possibilities for biological warfare, these technological developments have grave implications for peace and security."

We must view the Obama administration's cynical opposition to strengthening the Biological Weapons Convention because of the "regulatory burdens that verification would place on the American pharmaceutical industry and on the military's bio-defense research activities" as a dire international public health emergency, one which University of Illinois constitutional law professor Francis Boyle, the author of the 1989 Bioweapons Anti-Terrorism Act, has called "a catastrophe waiting to happen."

We proceed blindly along this path at our own peril.
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Re: Biowarfare Research: Lifting the Lid on America

Postby American Dream » Mon Feb 15, 2010 2:04 pm

http://www.nytimes.com/2010/02/14/magaz ... ogy-t.html

Do-It-Yourself Genetic Engineering
EDITED
February 10, 2010

Synthetic biologists want to break out of this cut-and-paste paradigm
altogether. They want to write brand-new genetic code, pulling
together specific genes or portions of genes plucked from a wide range
of organisms — or even constructed from scratch in a lab — and
methodically lacing them into a single set of genetic instructions.
Implant that new code into an organism, and you should be able to make
its cells do and produce things that nothing in nature has ever done
or produced before.

Synthetic biologists imagine nature as a manufacturing platform: all
living things are just crates of genetic cogs; we should be able to
spill all those cogs out on the floor and rig them into whatever new
machinery we want. It’s a jarring shift, making the ways humankind has
changed nature until now seem superficial.

Ideally you wouldn’t even need to know anything about DNA to manipulate it.

Over the past five years, iGEM teams have been collaboratively
amassing a centralized, open-source genetic library of more than 5,000
BioBricks, called the Registry of Standard Biological Parts. Each year
teams use these pieces of DNA to build their projects and also
contribute new BioBricks as needed. BioBricks in the registry range
from those that kill cells to one that makes cells smell like bananas.
The composition and function of each DNA fragment is cataloged in an
online wiki. Copies of the actual DNA are stored in a freezer at
M.I.T., and BioBricks are mailed to teams as red smudges of dehydrated
DNA.

IGEM has been grooming an entire generation of the world’s brightest
scientific minds to embrace synthetic biology’s vision — without
anyone really noticing, before the public debates and regulations that
typically place checks on such risky and ethically controversial new
technologies have even started.

The cost of synthesizing genes has dropped tremendously in the last
five years. (DNA is essentially an intricate chain of four different
chemical compounds, each represented by a letter; a gene can be
thousands of letters long. You can now send a sequence of those
letters to companies like Blue Heron Biotechnology, outside Seattle,
and get the actual gene back in the mail for a dollar, or less, per
letter.) Across the bay from City College, a University of California,
Berkeley iGEM team was building a piece of computer software that
allowed it to design genetic parts by dragging and dropping DNA
sequences together on the screen. Then, with the click of a button,
the software fed instructions to a liquid-handling robot in their lab
that executed various reactions and assembled each genetic part they
needed. It was like when you line up songs on iTunes and burn the
playlist on a CD. “We’re making way more DNA’s than we ever have
before, and we couldn’t have done it without the robot,” the Berkeley
team’s adviser told me.

The rise of synthetic biology only intensifies ethical and
environmental concerns raised by earlier forms of genetic engineering,
many of which remain unsettled. Given synthetic biology’s open-source
ethic, critics cite the possibility of bioterror: the malicious use of
DNA sequences posted on the Internet to engineer a new virus or more
devastating biological weapons. ETC Group, an international watchdog
that has raised complicated questions about synthetic biology since
its earliest days, also warns of the potential for “bio-error”: what
unintended and unimaginable consequences might result from deploying
all these freely reproducing, totally novel organisms into the world?

What if those living machines don’t work exactly as planned? “In a
way, you don’t have to have a working product to sell it,” says Jim
Thomas, a senior researcher at ETC Group. “You just have to have a
product that seems to work long enough to get into the open market.”
And, Thomas adds, as corporations continue to invest in organisms that
turn biomass into fuel or plastics, otherwise unlucrative crops will
suddenly be commoditized as feedstock for those synthetic organisms —
requiring more land to be cultivated and potentially displacing food
crops or people.

“This absolutely requires a public and political discussion,” Thomas
told me. “It’s going to change the alignments between very large
corporations. It’s going to change the ownership and patenting of life
forms. The field is growing at such a speed and industrial money is
flowing into it at such a speed — and here you have very excited,
smart, clever young people becoming wedded to these techniques. The
worry is, there’s not a lot of space left for reflection.”
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Re:

Postby psynapz » Mon Feb 15, 2010 2:45 pm

Hugo Farnsworth wrote:A BSL-4 facility in Galvestion???????????

WTF?

MSM said nothing about this during Ike.

Yup, they did. I remember it was a significant factor in early reporting.
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Re: Re:

Postby Hugo Farnsworth » Mon Feb 15, 2010 6:38 pm

psynapz wrote:
Hugo Farnsworth wrote:A BSL-4 facility in Galvestion???????????

WTF?

MSM said nothing about this during Ike.

Yup, they did. I remember it was a significant factor in early reporting.


My bad. I didn't watch much TV before the storm but I remember hearing nothing about it on the radio. But the article in the NYT (after the fact) is not very comforting. 140 mph winds? 30 ft above sea level? I suppose it's best that most people didn't know considering the Rita stampede.

I am going to try to look for some stuff on the local TV station's websites and the Chronicle.

BTW, do you live in Houston area?
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Re: Biowarfare Research: Lifting the Lid on America

Postby Uncle $cam » Mon Feb 15, 2010 7:03 pm

Given our crumbling country, how would you like to live 25 miles/40km from this:

NIAID ROCKY MOUNTAIN LABS BSL-4 facility

http://www3.niaid.nih.gov/labs/aboutlab ... aboratory/


Biodefense Research Section

Description of Research Program

The research focus of the Biodefense Research Laboratory comprises three areas:
Development of vaccines and antivirals against hemorrhagic fever viruses such as Ebola, Marburg and Lassa
Studies of the mechanism of vaccine-induced immune protection
Basic research to understand the mechanism of virus replication (entry) and neutralization

Ebola and Marburg viruses have been identified as the cause of several highly lethal outbreaks of hemorrhagic fever for which there is no treatment or cure. Therefore, vaccine studies are critically important for protection against infection. We developed a highly effective vaccine strategy for Ebola virus infection in non-human primates (Sullivan et al., Nature, 2000). A combination of primary immunization with plasmid DNA and boosting with adenoviral vectors containing Ebola genes generated protective immunity in cynomolgus macaques. The vaccine yielded 100% protective efficacy against Ebola infection and showed for the first time that protective immune responses could be generated in primates. The DNA vaccine is currently being tested in human trials conducted by the VRC Clinical Trials Core Laboratory. Subsequently, our laboratory has improved on earlier studies by demonstrating that protective immunity can be generated with a single shot of the adenoviral vector vaccine (Sullivan et al., Nature, 2003). Future studies will precisely define the dose and composition of a clinical Ebola vaccine product to be licensed for human use, and will also apply similar strategies to the development of protective vaccines against Marburg and Lassa viruses.

A second area of study in the Biodefense Research Section is the analysis of vaccine-induced immune responses. The mechanism of immune protection against Ebola virus infection is as yet unknown. Studies using knock-out mice have reported that NK-cells, cytolytic T-cells, or antibodies are each necessary for protection in the mouse model of Ebola virus infection. Other studies have shown using adoptive transfer that antibodies alone or T-cells alone are sufficient for protective immunity. Collectively, these investigations suggest that our understanding of immune protection against Ebola remains limited. Moreover, the mouse models of Ebola infection frequently fail to recapitulate important components of pathogenesis and immunity that are observed in primates. Therefore, we are using the studies of vaccine-induced protective immunity in nonhuman primates to help elucidate the precise mechanism(s) of immune protection against Ebola infection. Current studies under investigation are being conducted in nonhuman primates and utilize methods for selective inhibition of specific immunity such as T- and B-cell depletion, inhibition of T-cell help, and passive transfer of immune globulin. Using multicolor flow cytometry we are able to evaluate with high precision the quantity and quality of vaccine induced cellular responses by identifying distinct subsets of lymphocytes that are present in protected animals, and the kinetics with which they appear. Our goal is to combine the methods described to define and characterize the components required for immune protection against Ebola infection.

Our laboratory is also interested the basic biology underlying Ebola virus pathogenesis, virus-host interactions, and inhibition of virus replication. Ebola virus is a non-segmented negative strand RNA virus with a simple genome containing seven open reading frames. The virus replication cycle begins with binding of the envelope glycoprotein, GP, to a putative cell surface receptor(s) and entry into the host cell by fusion of viral and cell membranes. Strategies to interrupt the virus life cycle can be targeted to these early entry events or to later steps in the replication cycle. We are currently investigating the molecular basis for inhibition of virus entry by molecular inhibitors and neutralizing antibodies, and of genome replication and transcription by siRNA technology. We have developed and array of antibodies, both neutralizing and non-neutralizing, that are useful for characterizing GP structural changes and their functional consequences. We are using these tools to dissect the molecular events underlying Ebola GP interactions within the host. Our goal with these studies is to identify points in the Ebola virus replication cycle that are vulnerable antiviral and neutralization targets


? :evil:
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