Another One For The Transhumanist Scrapbook: Draconian Punishments

by Joseph P. Farrell


So many people sent me versions of this important and significant development that it was simply a kind of moral imperative that I alert readers here to it, and say something about it. In this case, there are four different articles, each of which reveals, almost immediately, what the new concern is:


Is Biotech Seeking Ways to Make People Suffer Eternally?

Should Biotech Make Life Hellish for Criminals? 

Enhanced Punishment: Can Technology Make Life Sentences Longer? 

Could we condemn criminals to suffer for hundreds of years? Biotechnology could let us extend convicts’ lives ‘indefinitely

When Dr. de Hart and I were writing Transhumanism: A Grimoire of Alchemical Agendas, one of the questions we were impelled to raise, one which the transhumanist movement itself raises repeatedly, is what does it mean to be “human”? And this, we implied, was not simply a philosophical question. Nor was it a question of biological or chemical “scientism” with its convenient, and largely useless, materialist reductionisms. It was a question of culture, society, jurisprudence, and morality

Within the transhumanist “vision” there is a common underlying theme, regardless of whether or not one accepts the “heaven scenarios” of such advocates like Ray Kurzweil, or the more sobering assessments of transhumanist researchers like Joel Garreau and their “hell scenarios”, for in both cases, the favored transhumanist “GRIN” technologies – genetics, robotics, information processing, and nano-technologies – open both favorable and horrific vistas of the future.

In this case, we are concerned with the horrific ones, for as the articles suggest, what if such technologies made life extension possible as a matter of judicial punishment? This unpleasant prospect, as the articles aver, is actually being not only entertained but its advocacy is even being implied in some circles. What if, in addition to this, other technologies are super-added to life extension, technologies of the “androgynous and alchemical fusion” of man and machine, to implant criminals with chips, to subject them to forms of “virtual torture” and suffering? Some transhumanists have envisioned the downloading and uploading of individual’s personal memories as a technique of virtual life extension. But what if such technologies could recover the memories of victims of crimes? Would criminals then be punished by making them relive in some sort of “virtual reality” the horrors of the crimes they committed on their victims? Could criminals of the future be sentenced to “life extension and ‘hard reliving’ of their crimes from the victim’s point of view” for “x” number of years, without hope of parole or reprieve? While such questions sound like science fiction, as the above articles point out, they are already being entertained, and they are being entertained, because the technologies impelling them are already under development.

Indeed, one can envision a state of development where such technologies were so advanced that a sentence of life in prison with “at hard virtual labor” would be so horrific, that the death penalty, far from being a thing to be avoided by defendants, might become a thing sought.

But there are yet other possibilities as well, possibilities that were, in fact, explored in the television science fiction series Babylon Five in the 1990s: the “death of personality.” In that series, convicted murderers are subjected to a kind of “death of the ego”: the erasure of the personality, memories, and emotions of the perpetrator

While some may view all of this favorably, and argue that it is “ethical,” I incline to the other opinion, and hold that it is barbaric, and a measure of the dehumanizing that such philosophies and technologies are inevitably bringing with them. I submit that such punishments are indeed “cruel and unusual” and little other than a form of torture.

 But whatever one’s opinion may be, the cultural transformation of culture and society that the transhumanists are championing or, in a few cases, decrying, are indeed hurtling down the tracks toward us and will force each of us to deal with the types of questions these articles are pointing out.


See you on the flip side.



The article first appeared here.


Municipal Waste Combustion Management for a Cleaner Environment

by Allen Williams


As government regulations continue to play an increased role in the nation's economy, there is a demand for cheaper energy sources to promote economic growth.  

America is committing vast land resources for the storage of Industrial and residential waste.  Municipalities must contract out or arrange for waste  transportation to landfill sites which amount to vast quantities of energy buried.  

Municipal waste is a growing problem in both rural and urban communities across the United States. Toxins are leached from the materials in the landfill over time that potentially threaten the water supply and many of today's modern components take centuries to decay in the earth. Landfills contain Combustible materials that could provide low cost energy for cities as well as improve the environment.

Photo: Land fill space a growing problem../

The average American now discards approximately 16-20 pounds of solid waste per day per person. This waste has traditionally been disposed of in landfills, which require huge tracts of land and have finite storage capacity.  Many landfills will have to close by 2040, increasing the cost of trash disposal and preventing the land from more productive use.

The Energy Information Administration (EIA) has noted that the energy content of solid waste in landfills has been steadily rising over the last decade, hitting 11.73 million Btu/ton in 2005. The heat content of interred waste provides the basis for developing an engineered fuel supporting many industrial applications such as the production of hydrocarbons, solvents, motor fuels, and even electric power generation.

A 2010 study(3) has found that emissions from landfills versus municipal waste combustion using EPA's life cycle assessment (LCA) model for the range and scenarios evaluated, that waste combustion outperforms land filling in terms of Green House Gas emissions regardless of landfill gas management techniques.

Innovative technologies can use buried waste as energy to convert bio-waste into needed products.  Recently, Sweden's 144 million Kristianstad biogas plant has successfully converted municipal bio-waste into methane for use in automobiles and heating, saving some $3.5 million per year. Biogas can be further processed to produce organic liquids and even motor grade fuels.

Municipal Waste can be converted into fuel pellets with combustion performance comparable to coal. The solid waste can be processed with an engineered heat content amenable to fluidized bed and other furnace combustion equipment.  Optimally, the pellets could be manufactured to a specific heat content. This is accomplished by feeding shredded rubber from scrap tires into a Cuber machine to produce fuel cubes of very high heating value, approximately 10,000 to 12,000 Btu/lb, suitable for utility power generation.

Developing a plan

The rising level of municipal waste provides incentive to develop alternative fuels but municipal waste contains many non-combustible components, some of which possess considerable recycle value. Recovery of these materials help to defer the cost of producing an engineered heat content fuel.  Figure 1 illustrates the potential economic return based on EPA waste content.

Figure 1 - Salvageable Materials And Byproducts Revenue

Locating a suitable waste transformation plant directly on a Landfill site saves added costs for property and waste transportation to a site as trucks are already servicing the  facility.  In natural gas producing landfills, a cheap supply of methane for hydrocarbon synthesis is readily available.

In cases where a bio-gas facility such as Johnson County Wastewater may be nearby, combustible waste sludge can be transported via pipeline for fueling a suitable fluidized bed boiler. The pipeline can pay for itself quickly as only the installation cost from the wastewater facility to the landfill need be considered.  Additionally, Industrial solvents such as methanol and other light hydrocarbons can be produced from the readily available methane feedstock along with steam and or electricity. 

Waste Site Considerations

An ideal plant site would be an 850-acre landfill of which approximately 770 acres are used for solid waste internment. Road infrastructure would already exist to handle the associated truck waste transport traffic. Only small infrastructure changes would be needed to support an onsite waste processing facility.

Waste transport vehicles would contain an average of 11 tons of municipal trash and make 1 to 3 trips per day to the site depending on weather and other factors. The landfill could receive as much as 5000 tons of trash per day, averaging nearly 19 trucks per hour.

Engineered fuels could be manufactured from this solid refuse on approximately 5 of the remaining 70 plus acres. The solid waste would be screened to remove various metals and other non-combustible materials before processing into specified heat content fuels.

Waste Separation process

Figure two illustrates dual waste handling units separating typical recyclable materials, shredding and blending recovered solids and vehicle tires from the municipal waste to produce a serviceable fuel pellet.  It is a time and motion illustration of the effort required to produce a 24% blend of solid waste and rubber.  The chart was developed from a real waste processing pilot operation by RCR Partners of Colorado during the early 1980's.

Since that time computer model studies have shown that a 50-50 waste blend of solids and scrap tires provided a better heat content fuel at 10,221 Btu/lb suitable for a small industrial boiler consuming approximately 30 tons of fuel pellets per hour.  The 50-50 blend represents only an incremental change in processing times.

The 2010 RCR industries salvageable Materials and Byproducts chart documents recovery revenues that are used to offset the cost of manufacturing an engineered fuel which is the basis of the Figure 2 chart.  From this study, recyclable materials savings, operating and labor costs can be estimated.

Figure 2 - Solids Separation and Fuel Pellet manufacture


RCR Material Flow

Bags enter the breaker machine from the truck where large boxes and bags are opened without damaging the contents. This permits the separation of light and heavy components. Food waste is removed prior to mechanical separation.

The solid waste moves through three mechanical separators upon entering the waste handling facility to remove glass, metal cans and plastic. Separation efficiency is greater than 90%.

Material next enters the first of two identical separators, all components less than 1-½” size pass through the first separator and are collected together with any metals in a common bin. These materials require further processing to segregate glass and metal

Separator No 3 removes all fractions less than 3" x 8”. Plastics fall into a collection bin exiting the 3rd separator.

The remaining material enters the shredder and is now all light fraction material.

The shredder slices the solid waste into approximately a ¾” size. The material passes through a cyclone separator to remove any dust generated by the shredding operation. The material can then be moistened and compressed by a Cuber machine into approximately 1-1/2" x 2" size fuel pellets.

The pellets may then be conveyed to storage vessels.

Photo: Fuel Pellets conveyed to Storage


Economics

Company reports are often good sources of economic cost data. Our fuel processing cost is estimated from an RCR Partners pilot plant study for the year's 1982-'83. The ordinary expense average for these years was $2,308,500 per year and defines the fixed costs. The Jan. '84 - Mar. '11 inflation rate was 146.7%, adjusting the ordinary expenses to present costs gives $5,694,244 per year.

The following utility rates were used in the economic evaluation: Coal at $55.00/ton, electricity at 7.3 cents per kilowatt, plant water for 3.2 cents a gallon and engineered fuel expenses according to the following cost relation.  Fuel Cost/(ton) = X% * fixed cost + (1-X)% * rubber + processing

The base rate is calculated from the total production cost minus the revenue from salvageable materials separated out during the manufacturing process, i.e.  [$Cost - $Salvage]/Total Tons = $Cost/ton

The salvageable material quantities from waste separation that can be re-sold are indicated in figures 1and 2.  Ferrous metal scrap pays a max of $250/ton, Aluminum $0.75/lb and plastics $150/ton.  Salvageable tire steel belt is 2.5 lbs/tire:

Details of computer simulated quantities and expected margins in the production of an organic solvent using engineered fuel pellets may be found in the July 2012 issue of Chemical Engineering, Vol 119, No. 7


Conclusions

One of the most significant features of engineered fuels is the ability to reduce the quantity of sulfur that must be scrubbed out of atmospheric releases during combustion.  In our simulation, the computer model predicted a 20.67% reduction in SO2 emissions..

Mercury is virtually eliminated from stack gas emissions and other airborne contaminants can be significantly reduced through controlled waste blending.

Combusting Municipal waste in a controlled environment not only alleviates the need for further land repositories but may also facilitate recovery of burnable materials from many existing landfills.

Literature Cited:


1. "Methodology for Allocating Municipal Solid Waste to Biogenic and Non-Biogenic Energy", Energy Information Administration, Office of Coal, Nuclear, Electric and Alternate Fuels U.S., May 2007 Report

2. “Evaluating Green Projects – Modeling Improves Economic Benefits”, A. Williams, K. Dunwoody, Chemical Engineering – 119, 7, July 2012

3.   "Life-Cycle Assessment of Waste Management Greenhouse Gas Emissions Using Municipal Waste Combustor Data", J. Envir. Engr. 136, 749 (2010); doi:10.1061/(ASCE)EE.1943-7870.0000189 (7 pages),Brian Bahor, Michael Van Brunt, P.E., Keith Weitz, and Andrew Szurgot

4. "Multisolid Fluidized Bed Combustion", H. Nack, R.D. Litt, B.C. Kim, Chemical Engineering Progress, Jan 1984

5. "Energy Recovery from Fluidized Bed Combustion", Robert J. Sneyd, Chemical Engineering Progress, Jan 1984

6. "Methodology for Allocating Municipal Solid Waste to Biogenic and Non-Biogenic Energy", Energy Information Administration, Office of Coal, Nuclear, Electric and Alternate Fuels, May 2007 Report


Deadly Medicine Creating the Master Race

by John Carlos Cantu           


U-M Taubman Health Sciences Library exhibit presents a chilling look at Nazi ideology.

The 1938 words of Dr. Joseph Goebbels, Nazi minister of propaganda, stand above the display panels of what is undoubtedly the most somber exhibit Ann Arbor has seen at the University of Michigan Taubman Health Sciences Library.  Goebbel’s quote runs as follows: “Our starting point is not the individual, and we do not subscribe to the view that one should feed the hungry, give drink to the thirsty, or clothe the naked…. Our objectives are entirely different: We must have a healthy people in order to prevail in the world.” 

These words are chilling and they’re more than an adequate rationale for this heart-rending investigation into a politics that sought to implement one of the most perverse policies in history. 

As Mary Beth Reilly, writer for the U-M’s Center for the History of Medicine, says in the display’s gallery statement, “The Nazi regime was founded upon the conviction that ‘inferior races’ and individuals had to be eliminated from German society so that the fittest ‘Aryans’ could thrive. 

“By the end of World War II, six million Jews and millions of others—among them Roma and Sinti (Gypsies), people with disabilities, homosexuals, and others belonging to ethnic groups deemed inferior—had been persecuted and murdered.”  And as Alexandra Minna Stern, Zina Pitcher Collegiate Professor of the History of Medicine and Associate Director of the Center for the History of Medicine at the U-M Medical School, adds, “The exhibition is a visually powerful experience for viewers that shows how the doctrine of racial hygiene was taken to its most heinous extremes.” 

Indeed. And as the exhibit pointedly illustrates, there’s more than enough blame to go around. For the exhibit begins with a panel illustrating the various programs from countries around the world (including the United States) advocating various eugenic schemes at the turn of the 20th century whose “racial hygiene” included programs in population policy, public health education, and government-funded research whose ends (even if they weren’t remotely the same) clearly showed an undeniable bias.  

The rediscovery of Austrian botanist Gregor Mendel’s genetics experiments in 1900 coupled with the increasingly fashionable “Social Darwinism” of British philosopher cum sociologist Herbert Spencer, whose catchphrase “survival of the fittest” was being bandied about, led to increasing public prestige in the efforts to stabilize public policy issues that emerged with increasing industrialization and urbanization. This was, in retrospect, a philosophical and political slippery slope that was in part absorbed in the ideology and practice of the newly emergent Nazi party of the 1920s. 

From the early 1930s through the balance of the Nazi regime, there were repeated campaigns to rid German society of what they viewed as biological threats. As “Deadly Medicine” clearly shows, this policy absorbed the efforts and energies of many of the nation’s most talented doctors, psychiatrists, anthropologists, and medically trained geneticists, as well as social planners and party functionaries at every level.  [And soon to be repeated in the form of Obamacare - ED] 

What started as a secret campaign to eliminate the weak and infirm disguised as medical assistance metastasized into a full-fledge program of eradication under the pressure of World War II. Ultimately, this so-called “sanitary campaign” finally took form as a genocide that we now know as the Holocaust, resulting in the near total annihilation of Europe’s Jewish population. 

To its credit, “Deadly Medicine” doesn’t pull any punches. Its juxtaposition of scientific certitude and racial hatred are handled as responsibly as the topics deserve. 

By naming names, dates, and events—as well as providing significant visual evidence—the exhibit takes the full measure of this circumstance where those in charge of healing and sustenance distorted their responsibilities until their lifework turned into a horror whose pain continues to this day.  

It’s certainly enough pain for Professor Stern to remind us that the example of this massive failure of science, technology, tolerance, and ultimately compassion, “raises weighty questions about the potential benefits and harms of genetic and reproductive technologies today.” And it’s on this cautionary note that the solemn exhibit rightfully concludes.

 

 




“It’s certainly enough pain for Professor Stern to remind us that the example of this massive failure of science, technology, tolerance, and ultimately compassion, “raises weighty questions about the potential benefits and harms of genetic and reproductive technologies today.” And it’s on this cautionary note that the solemn exhibit rightfully concludes.”  The article first appeared here. - DNI


Human Experiments: A Chronology of Human Research

by Vera Hassner Shara


6th century B.C.: Meat and vegetable experiment on young Jewish prisoners in Book of Daniel.

5th century B.C: "Primum non nocere" ("First do no harm"), medical ethics standard attributed to Hippocrates. This Oath became obligatory for physicians prior to practicing medicine in the 4th century AD

1st century B.C. Cleopatra devised an experiment to test the accuracy of the theory that it takes 40 days to fashion a male fetus fully and 80 days to fashion a female fetus. When her handmaids were sentenced to death under government order, Cleopatra had them impregnated and subjected them to subsequent operations to open their wombs at specific times of gestation. [http://www.jlaw.com/Articles/NaziMedExNotes.html#1]

12th century: Rabbi and physician Maimonides' Prayer: "May I never see in the patient anything but a fellow creature in pain."

1796 Edward Jenner injects healthy eight-year-old James Phillips first with cowpox then three months later with smallpox and is hailed as discoverer of smallpox vaccine.

1845-1849: J. Marion Sims, "the father of gynecology" performed multiple experimental surgeries on enslaved African women without the benefit of anesthesia. After suffering unimaginable pain, many lost their lives to infection. One woman was made to endure 34 experimental operations for a prolapsed uterus. http://www.coax.net/people/lwf/jm_sims.htm

1865: French physiologist Claude Bernard publishes "Introduction to the Study of Human Experimentation," advising: "Never perform an experiment which might be harmful to the patient even though highly advantageous to science or the health of others."

1896: Dr. Arthur Wentworth performed spinal taps on 29 children at Children's Hospital, Boston, to determine if the procedure was harmful. Dr. John Roberts of Philadelphia, noting the non-therapeutic indication, labeled Wentworth's procedures "human vivisection."

1897: Italian bacteriologist Sanarelli injects five subjects with bacillus searching for a causative agent for yellow fever.

1900: Walter Reed injects 22 Spanish immigrant workers in Cuba with the agent for yellow fever paying them $100 if they survive and $200 if they contract the disease. 

1900: Berlin Code of Ethics. Royal Prussian Minister of Religion, Education, and Medical Affairs guaranteed that: "all medical interventions for other than diagnostic, healing, and immunization purposes, regardless of other legal or moral authorization are excluded under all circumstances if (1) the human subject is a minor or not competent due to other reasons; (2) the human subject has not given his unambiguous consent; (3) the consent is not preceded by a proper explanation of the possible negative consequences of the intervention."http://www.geocities.com/artnscience/00berlincode.pdf

1906: Dr. Richard Strong, a professor of tropical medicine at Harvard, experiments with cholera on prisoners in the Philippines killing thirteen.

1913: Pennsylvania House of Representatives recorded that 146 children had been inoculated with syphilis, "through the courtesy of the various hospitals" and that 15 children in St. Vincent's House in Philadelphia had had their eyes tested with tuberculin. Several of these children became permanently blind. The experimenters were not punished.

1915: A doctor in Mississippi, working for the U.S. Public Health Office produces Pellagra in twelve Mississippi inmates in an attempt to discover a cure for the disease

1919-1922: Testicular transplant experiments on five hundred prisoners at San Quentin.

1927: Carrie Buck of Charlottesville is legally sterilized against her will at the Virginia Colony Home for the Mentally Infirm. Carrie Buck was the mentally normal daughter of a mentally retarded mother, but under the Virginia law, she was declared potentially capable of having a "less than normal child." By the 1930s, seventeen states in the U.S. have laws permitting forced sterilization.  The settlement of Poe v. Lynchburg Training School and Hospital (same institution, different name) in 1981 brought to an end the Virginia law. It is estimated that as many as 10,000 perfectly normal women were forcibly sterilized for "legal" reasons including alcoholism, prostitution, and criminal behavior in general.

1931: Lubeck, Germany, 75 children die in from pediatrician's experiment with tuberculosis vaccine.  

Germany adopts "Regulation on New Therapy and Experimentation" requiring all human experiments to be preceded by animal experiments. This law remained in effect during the Nazi regime.

1931: Dr. Cornelius Rhoads, a pathologist, conducted a cancer experiment in Puerto Rico under the auspices of the Rockefeller Institute for Medical Investigations. Dr. Rhoads has been accused of purposely infecting his Puerto Rican subjects with cancer cells. Thirteen of the subjects died. A Puerto Rican physician uncovered the experiment an investigation covered-up the facts. Despite Rhoads' hand written statements that the Puerto Rican population should be eradicated, Rhoads went on to establish U.S. Army Biological Warfare facilities in Maryland, Utah, and Panama, and was later named to the U.S. Atomic Energy Commission. Rhoads was also responsible for the radiation experiments on prisoners, hospital patients, and soldiers. The American Association for Cancer Research honored him by naming its exemplary scientist award the Cornelius Rhoads Award.

1932-1972: U.S. Public Health Service study in Tuskegee, Alabama of more than 400 black sharecroppers observed for the natural course of untreated syphilis.

1932: Japanese troops invade Manchuria. Dr. Shiro Ishii, a prominent physician and army officer begins preliminary germ warfare experiments. 

1936: Japan's Wartime Human Biowarfare Experimentation Program.

1938: Japan establishes Unit 731 in Pingfan, 25 km. from Harbin. Unit 731, a biological-warfare unit disguised as a water-purification unit, is formed outside the city of Harbin.

1939: Third Reich orders births of all twins be registered with Public Health Offices for purpose of genetic research.  [[One twin experimented on, the other twin used as a genetic “control”. -- DNI]]

1939: Twenty-two children living at the Iowa Soldiers' Orphans' Home in Davenport were the subjects of the "monster" experiment that used psychological pressure to induce children who spoke normally to stutter. It was designed by one of the nation's most prominent speech pathologists, Dr. Wendell Johnson, to test his theory on the cause of stuttering.

1940: Poisonous gas experiments at Unit 731 (Japan). One experiment conducted September 7-10, 1940, on 16 Chinese prisoners who were exposed to mustard gas in a simulated battle situation.

1940-1941: Unit 731 (Japan) used aircraft to spread cotton and rice husks contaminated with the black plague at Changde and Ningbo, in central China. About 100 people died from the black plague in Ningbo as a result.

1940's: In a crash program to develop new drugs to fight Malaria during World War II, doctors in the Chicago area infected nearly 400 prisoners with the disease. Although the Chicago inmates were given general information that they were helping with the war effort, they were not informed about the nature of the experiment. Nazi doctors on trial at Nuremberg cited the Chicago studies as precedents to defend their own research aimed at aiding the German war effort.

1941: Sterilization experiments at Auschwitz.

1941-1945: Typhus experiments at Buchenwald and Natzweiler concentration camps.

1941: Dr. William c. Black inoculated a twelve month old baby with herpes. He was criticized by Francis Payton Rous, editor of the Journal of Experimental Medicine, who called it "an abuse of power, an infringement of the rights of an individual, and not excusable because the illness which followed had implications for science." Dr. Rous rejected outright the fact that the child had been "offered as a volunteer."

1942 - 1945: Unit 731 (Japan). Ishii begins "field tests" of germ warfare and vivisection experiments on thousands of Chinese soldiers and civilians. Chinese people who rebelled against the Japanese occupation were arrested and sent to Pingfan where they became human guinea pigs; there is evidence that some Russian prisoners were also victims of medical atrocities. "I cut him open from the chest to the stomach and he screamed terribly and his face was all twisted in agony. He made this unimaginable sound, he was screaming so horribly. But then finally he stopped. This was all in a day's work for the surgeons, but it really left an impression on me because it was my first time." - NYT

These prisoners were called 'maruta' (literally 'logs') by the Japanese. After succumbing to induced diseases - including bubonic plague, cholera, anthrax - the prisoners were usually dissected while still alive, their bodies then cremated within the compound. Tens of thousands died. The atrocities were committed by some of Japan's most distinguished doctors recruited by Dr. Ishii.

1942: High altitude or low pressure experiments at Dachau concentration camp.

1942: Harvard biochemist Edward Cohn injects sixty-four Massachusetts prisoners with beef blood in U.S. Navy-sponsored experiment.

1942: Japanese sprayed cholera, typhoid, plague, and dysentery pathogens in the Jinhua area of Zhejian province (China). A large number of Japanese soldiers also fell victim to the sprayed diseases.

1942-1943: Bone regeneration and transplantation experiments on female prisoners at Ravensbrueck concentration camp.

1942-1943: Freezing experiments at Dachau concentration camp.

1943 Refrigeration experiment conducted on sixteen mentally disabled patients who were placed in refrigerated cabinets at 30 degree Farenheit, for 120 hours, at University of Cincinnati Hospital., "to study the effect of frigid temperature on mental disorders."

1942-1943: Coagulation experiments on Catholic priests at Dachau concentration camp.

1942-1944: U.S. Chemical Warfare Service conducts mustard gas experiments on thousands of servicemen.

1942-1945: Malaria experiments at Dachau concentration camp on more than twelve hundred prisoners.

1943: Epidemic jaundice experiments at Natzweiler concentration camp.

1943-1944: Phosphorus burn experiments at Buchenwald concentration camp.

1944: Manhattan Project injection of 4.7 micrograms of plutonium into soldiers at Oak Ridge, TN.

1944: Seawater experiment on sixty Gypsies who were given only saltwater to drink at Dachau concentration camp.

1944-1946: University of Chicago Medical School professor Dr. Alf Alving conducts malaria experiments on more than 400 Illinois prisoners.

1945: Manhattan Project injection of plutonium into three patients at Billings Hospital at University of Chicago.

1945: Malaria experiment on 800 prisoners in Atlanta.

1946: Opening of Nuremberg Doctors Trial by U.S. Military Tribunal.

1945: Japanese troops blow up the headquarters of Unit 731 in final days of Pacific war. Ishii orders 150 remaining ''logs'' (i.e., human beings) killed to cover up their experimentation. Gen. Douglas MacArthur is named commander of the Allied powers in Japan.

1946: U.S. secret deal with Ishii and Unit 731 leaders cover up of germ warfare data based on human experimentation in exchange for immunity from war-crimes prosecution.

1946-1953: Atomic Energy Commission sponsored study conducted at the Fernald school in Massachusetts. Residents were fed Quaker Oats breakfast cereal containing radioactive tracers.

1946: Patients in VA hospitals are used as guinea pigs for medical experiments. In order to allay suspicions, the order is given to change the word "experiments" to "investigations" or "observations" whenever reporting a medical study performed in one of the nation's veteran's hospitals.

1947: Colonel E.E. Kirkpatrick of the U.S. Atomic Energy Commission issues a secret document (Document 07075001, January 8, 1947) stating that the agency will begin administering intravenous doses of radioactive substances to human subjects.

1947: The CIA begins its study of LSD as a potential weapon for use by American intelligence. Human subjects (both civilian and military) are used with and without their knowledge.

1947: Judgment at Nuremberg Doctors Trial sets forth "Permissible Medical Experiments" i.e., the Nuremberg Code, which begins: "The voluntary consent of the human subject is absolutely essential."

1949: Intentional release of radiodine 131 and xenon 133 over Hanford Washington in Atomic Energy Commission field study called "Green Run."

1949: Soviet Union's war crimes trial of Dr. Ishii's associates (Japan).

1949-1953: Atomic Energy Commission studies of mentally disabled school children fed radioactive isotopes at Fernald and Wrentham schools.

1940s-1950s: "psychic driving" and "mental departterning" experiments conducted by Dr. Ewen Cameron, depriving patients of sleep, using massive ECT combined with psychoactive drugs such as, LSD. After his "treatments" patients were unable to function. In the 1950's Dr.Cameron's experiments were sponsored by the CIA.

1950: Dr. Joseph Stokes of the University of Pennsylvania infects 200 women prisoners with viral hepatitis.

1950: U.S. Army secretly used a Navy ship outside the Golden Gate to spray supposedly harmless bacteria over San Francisco and its outskirts. Eleven people were sickened by the germs, and one of them died.

1951-1960: University of Pennsylvania under contract with U.S. Army conducts psychopharmacological experiments on hundreds of Pennsylvania prisoners.

1952-1974: University of Pennsylvania dermatologist Dr. Albert Kligman conducts skin product experiments by the hundreds at Holmesburg Prison; "All I saw before me," he has said about his first visit to the prison, "were acres of skin."

1952: Henry Blauer injected with a fatal dose of mescaline at New York State Psychiatric Institute of Columbia University. U.S. Department of Defense, the sponsor, conspired to conceal evidence for 23 years.

1953 Newborn Daniel Burton rendered blind at Brooklyn Doctor's Hospital due to high oxygen study on RLF.

1953-1957: Oak Ridge (TN)-sponsored injection of uranium into eleven patients at Massachusetts General Hospital in Boston.

1953-1960: CIA brainwashing experiments with LSD at eighty institutions on hundreds of subjects in a project code named "MK-ULTRA."

1953-1970: U.S. Army experiments with LSD on soldiers at Fort Detrick, Md.

1954-1974: U.S. Army study of 2,300 Seventh-Day Adventist soldiers in 157 experiments code named "Operation Whitecoat."

1950s - 1972: Mentally disabled children at Willowbrook School (NY) were deliberately infected with hepatitis in an attempt to find a vaccine. Participation in the study was a condition for admission to institution.

1956: Dr. Albert Sabin tests experimental polio vaccine on 133 prisoners in Ohio.

1958-1962: Spread of radioactive materials over Inupiat land in Point Hope, Alaska in Atomic Energy Commission field study code named "Project Chariot."

1962: Thalidomide withdrawn from the market after thousands of birth deformities blamed in part on misleading results of animal studies; the FDA thereafter requires three phases of human clinical trials before a drug can be approved for the market.

1962 to 1966, a total of 33 pharmaceutical companies tested 153 experimental drugs at Holmesburg prison (PA) alone.

1962-1980 Pharmaceutical companies conduct phase I safety testing of drugs almost exclusively on prisoners for small cash payments.

1962: Injection of live cancer cells into 22 elderly patients at Jewish Chronic Disease Hospital in Brooklyn. Administration covered up, NYS licensing board placed the principal investigator on probation for one year. Two years later, American Cancer Society elected him Vice President.

1962: Stanley Milgram conducts obedience research at Yale University.

1963: NIH supported researcher transplants chimpanzee kidney into human in failed experiment.

1963-1973: Dr. Carl Heller, a leading endocrinologist, conducts testicular irradiation experiments on prisoners in Oregon and Washington giving them $5 a month and $100 when they receive a vasectomy at the end of the trial.

1964: World Medical Association adopts Helsinki Declaration, asserting "The interests of science and society should never take precedence over the well being of the subject."

 1965-1966: University of Pennsylvania under contract with Dow Chemical conducts dioxin experiments on prisoners at Holmesburg.

 1966: Henry Beecher's article "Ethics and Clinical Research" in New England Journal of Medicine.

 1966: U.S. Army introduces bacillus globigii into New York subway tunnels in field study.

 1966: NIH Office for Protection of Research Subjects ("OPRR") created and issues Policies for the Protection of Human Subjects calling for establishment of independent review bodies later known as Institutional Review Boards.

1967: British physician M.H. Pappworth publishes "Human Guinea Pigs," advising "No doctor has the right to choose martyrs for science or for the general good."

1969: Judge Sam Steinfield's eloquent dissent in Strunk v. Strunk, 445 S.W.2d 145, the first judicial suggestion that the Nuremberg Code should influence American jurisprudence.

1969. Milledgeville Georgia, investigational drugs tested on mentally disabled children. No institutional approval.

1969: San Antonio Contraceptive Study conducted on 70 poor Mexican-American women. Half received oral contraceptives the other placebo. No informed consent.

1973 Ad Hoc Advisory Panel issues Final Report of Tuskegee Syphilis Study, concluding "Society can no longer afford to leave the balancing of individual rights against scientific progress to the scientific community."

1974: National Research Act establishes National Commission for the Protection of Human Subjects and requires Public Health Service to promulgate regulations for the protection of human subjects.  [[The NRA also mandated that then-Secretary of DHHS Casper Weinburger appoint a committee to determine the 'ethical principles the US government should use in dealing with the use of human subjects in research.  Thus the National Commission was established in 1975, consisting of 11 appointed members, only one (Art Caplan) with a Ph.D. in philosophy (ethics is a subfield of philosophy). (Caplan is now on the Board of Trustees of the transhumanist Institute for Ethics and Emerging Technologies (IEET)). In 1978/9 the National Commission submitted its Belmont Report -- the formal 'birth of bioethics' -- denoting three ethical principles:  respect for persons (which was rapidly replaced by autonomy), justice and beneficence (all oddly defined).  The NRA also mandated that the Belmont Report be incorporated on the first page of the revised OPRR federal regulations (now OHRP), done in 1981.  In those OPRR federal regulations, the 'human embryo' is nowhere defined as a 'subject of research' or otherwise -- thus legally does not exist.  Two false scientific definitions are incorporated into those OPRR regulations:  both 'pregnancy and fetus' are mis-defined as 'beginning at implantation'.  Real natural normal pregnancy begins at fertilization in the woman's fallopian tube (not in her uterus), and the 'fetal period' doesn't really begin until the beginning of 9 weeks post-fertilization. Thus theoretically,  according to these federal regulations (still operative as the OHRP regulations), abortions, the use of abortifacients, human embryo flushing, research on all human embryos in vitro in IVF/ART facilities can be 'legally' performed through 8 weeks post-fertilization. The USCCB official who inserted these two false scientific definitions was Richard Doerflinger. Of course, these federal regulations would also allow for all the genetic engineering (including synthetic biology and nanotechnology) of human embryos -- in vivo or in vitro -- so popular today.  -- DNI]]

1975: The Department of Health, Education and Welfare (DHEW) raised NIH's 1966 Policies for the Protection of Human subjects to regulatory status. Title 45 of the Code of Federal Regulations, known as "The Common Rule," requires the appointment and utilization of institutional review boards (IRBs).

1976: National Urban League holds National Conference on Human Experimentation, announcing "We don't want to kill science but we don't want science to kill, mangle and abuse us."

1978: Experimental Hepatitis B vaccine trials, conducted by the CDC, begin in New York, Los Angeles and San Francisco. Ads for research subjects specifically ask for promiscuous homosexual men.

1979: National Commission issues Belmont Report setting forth three basic ethical principles: respect for persons, beneficence, and justice.

1980: The FDA promulgates 21 CFR 50.44 prohibiting use of prisoners as subjects in clinical trials shifting phase I testing by pharmaceutical companies to non-prison population.

1981: Leonard Whitlock suffers permanent brain damage after deep diving experiment at Duke University.

1986: Congressional subcommittee holds one-day hearing in Washington, called by Rep. Pat Williams of Montana, aimed at determining whether U.S. prisoners of war in Manchuria were victims of germ-warfare experimentation. Hearing is inconclusive.

1981-1996: Protocol 126 at Fred Hutchinson Cancer Center in Seattle.

1987: Supreme Court decision in United States v. Stanley, 483 U.S. 669, holding soldier given LSD without his consent could not sue U.S. Army for damages.

1987:" L-dopa challenge and relapse" experiment conducted on 28 U.S. veterans who were subjected to psychotic relapse for study purposes at the Bronx VA.

1990: The FDA grants Department of Defense waiver of Nuremberg Code for use of unapproved drugs and vaccines in Desert Shield.

1991: World Health Organization announces CIOMS Guidelines which set forth four ethical principles: respect for persons, beneficence, nonmaleficence and justice.

1991: Tony LaMadrid commits suicide after participating in study on relapse of schizophrenics withdrawn from medication at UCLA.

1993: Kathryn Hamilton dies 44 days after participating in breast cancer experiment at Fred Hutchinson Cancer Center in Seattle.

1994. The Albuquerque Tribune publicizes 1940s experiments involving plutonium injection of human research subjects and secret radiation experiments. Indigent patients and mentally retarded children were deceived about the nature of their treatment.

1994. President Clinton appoints the Advisory Commission on Human Radiation Experiments (ACHRE) The ACHRE Report http://tis.eh.doe.gov/ohre/roadmap/achre/index.html

1995. U.S. Department of Energy (DOE) published Human Radiation Experiments, listing 150 plus an additional 275 radiation experiments conducted by DOE and the Atomic Energy Commission, during the 1940s - 1970s. http://tis.eh.doe.gov/ohre/roadmap/experiments/0491doca.html#0491_List

1995: 19-year-old University of Rochester student Nicole Wan dies after being paid $150 to participate in MIT-sponsored experiment to test airborne pollutant chemicals.

1995. President Clinton appoints the National Bioethics Advisory Commission.

1995: NYS Supreme Court rules (TD v NYS Office of Mental Health) against the state's policy of conducting nontherapeutic experiments on mentally incapacitated persons - including children - without informed consent. Justice Edward Greenfield ruled that parents have no authority to volunteer their children: "Parents may be free to make martyrs of themselves, but it does not follow that they may make martyrs of their children."

1995: Thirty-four healthy, previously non-aggressive New York City minority children, boys aged 6 to 11 years old, were exposed to fenfluramine in a nontherapeutic experiment at the New York State Psychiatric Institute. The children were exposed to this neurotoxic drug to record their neurochemical response in an effort to prove a speculative theory linking aggression to a biological marker.

1996. Cleveland Plain Dealer investigative report series, 'Drug Trials: Do People Know the Truth About Experiments,' December 15 to 18, 1996. The Plain-Dealer found: of the "4,154 FDA inspections of researchers testing new drugs on people [since 1977] . . . more than half the researchers were cited by FDA inspectors for failing to clearly disclose the experimental nature of their work."

1996: Yale University researchers publish findings of experiment that subjected 18 stable schizophrenia patients to psychotic relapse in an amphetamine provocation experiment at West Haven VA.

1997. President Clinton issues a formal apology to the subjects of the Tuskegee syphilis experiments. NBAC continues investigation into genetics, consent, privacy, and research on persons with mental disorders.

1997. Researchers at the University of Cincinnati publish findings of experiment attempting to create a "psychosis model" on human beings at the Cincinnati VA. Sixteen patients, experiencing a first episode schizophrenia, were subjected to repeated provocation with amphetamine. The stated purpose was to produce "behavioral sensitization. This process serves as a model for the development of psychosis, but has been little studied in humans. Symptoms, such as severity of psychosis and eye-blink rates, were measured hourly for 5 hours."

1997. U.S. government sponsored placebo-controlled experiment withholds treatment from HIV infected, pregnant African women. NY Times, Sept. 18.

1997. Victims of unethical research at major U.S. medical centers - including the NIMH - testify before the National Bioethics Advisory Commission, Sept. 18.

1997. FDA Modernization Act gives pharmaceutical companies a huge financial incentive - a 6 month patent exclusivity extension - if they conduct drug tests on children. The incentive can yield $900 million.

1998. National Bioethics Advisory Commission (NBAC) Report. Research Involving Subjects with Mental Disorders That May Affect Decisionmaking Capacity. November 12,

1998 http://bioethics.georgetown.edu/nbac/capacity/TOC.htm

1998: The Japanese government has never formally apologized for Unit 731's activities, and did not even admit to its existence until August 1998, when the Supreme Court ruled that the existence of the unit was accepted in academic circles.

1998. Complaint filed with OPRR about experiments that exposed non-violent children in New York City to fenfluramine to find a predisposition to violence.

1998: Boston Globe (four part) series, "Doing Harm: Research on the Mentally Ill" shed light on the mistreatment and exploitation of schizophrenia patients who have been subjected to relapse producing procedures in unethical experiments.

1999: Nine month-old Gage Stevens dies at Children's Hospital in Pittsburgh during participation in Propulsid clinical trial for infant acid reflux.

1999: 18-year-old Jesse Gelsinger dies after being injected with 37 trillion particles of adenovirus in gene therapy experiment at University of Pennsylvania.

1999: Director of National Institute of Mental Health suspends 29 clinical trials that failed to meet either ethical or scientific standards.

2000: University of Oklahoma melanoma trial halted for failure to follow government regulations and protocol.

2000: OPRR becomes Office of Human Research Protection ("OHRP") and made part of the Department of Health and Human Services.

2000: President Clinton implements the Energy Employees Occupational Illness Compensation Act of 2000, which authorized compensation for thousands of Department of Energy workers who sacrificed their health in building the nation's nuclear defenses.

2000: The Washington Post (6 part) series, "Body Hunters" exposes unethical exploitation in experiments conducted by U.S. investigators in underdeveloped countries. Part 4 dealt with U.S. government funded, genetic experiments conducted by Harvard University in rural China.
http://www.washingtonpost.com/wp-dyn/articles/A26797-2000Dec19.html

2001: A biotech company in Pennsylvania asks the FDA for permission to conduct placebo trials on infants in Latin America born with serious lung disease though such tests would be illegal in U.S.

2001: Ellen Roche, a healthy 27-year old volunteer, dies in challenge study at Johns Hopkins University in Baltimore, Maryland.

2001: April 4, Elaine Holden-Able, a healthy retired nurse, consumed a glass of orange juice that had been mixed with a dietary supplement for the sake of medical research. This Case Western University Alzheimer's experiment, financed by the tobacco industry, wound up killing her in what was called a ''tragic human error.'' Federal Office of Human Research Protections did not interview hospital staff, mostly accepted hospital's internal report, imposed no penalty, and closed the case and did not mention the death in its letter of determination. http://ohrp.osophs.dhhs.gov/detrm_letrs/nov01f.pdf

2001: Maryland Court of Appeals renders a landmark decision affirming "best interest of the individual child" as a standard for medical research involving children. The Court unequivocally prohibited nontherapeutic experimentation on children. (Higgins and Grimes v. Kennedy Krieger Institute).The case involved exposure of babies and small children to lead poisoning in EPA funded experiment. (http://www.courts.state.md.us/opinions/coa/2001/128a00.pdf)

 

 


Note:  A very sobering chronology of unethical human research -- at least such that was reported -- well worth contemplating -- especially now that even our federal agencies are pushing to do away with the 'informed consent' requirement as the only way to get 'data';  see, e.g.: 

**Medical Research Stakeholders Seek to Overturn Informed Consent Protections;  Part 3 of 4, at:  http://www.ahrp.org/cms/content/view/928/9/

**Medical Research Stakeholders Seek to Overturn Informed Consent Protections;  Part 2 of 4, at:  http://www.ahrp.org/cms/content/view/927/81/

**Another View Academics for Informed Consent, at:  http://www.ahrp.org/cms/content/view/926/99/

**Medical Research Stakeholders Seek to Overturn Informed Consent Protection;  Part 1 of 4, at:  http://www.ahrp.org/cms/content/view/925/81/

**OHRP Caves Under SUPPORT Pressure Re: oxygen experiment tiny premature babies, at:  http://www.ahrp.org/cms/content/view/924/81/

Note especially the unethical research pre-World War II through 2001 -- all performed supposedly for 'beneficent, altruistic or 'national security' reasons, mostly by government agencies, esteemed academic medical facilities, prominent investigators, pharmaceutical companies -- mostly without 'informed consent' or the victims' knowledge, on vulnerable children, prisoners, the elderly, mentally ill and retarded, political and ethnic opponents, Third World populace, etc.  Given the current explosion of especially genetic and genetic engineering research -- and the concomitant explosion of scientific fraud and unethical experiments -- all need to be aware of these very disturbing precedents.  'Data' at any cost.  'Bioethics' would approve most of this as being 'for the greater good'.  However, there are other 'ethics' insisting that 'the ends never justify the means'.  See especially 1974, above.  Please read carefully, all the way through to the end.  I bet you won't be able to.  Note:  'VA' used above usually refers to 'Veterans Administration'.  . -- DNI]