Q. Isn't chloracne the only evidence of dioxin exposure?
A: Public concern about effects of dioxin on human health was heightened in 1976
following an accident at Seveso in Italy, when an explosion at a chemical factory caused
the release of high levels of TCDD (dioxin). The most commonly reported effects on humans
following this accident and other incidents of high dioxin exposure was a skin rash called
chloracne.
Since then numerous animal experiments and several epidemiological studies in humans
have shown that dioxin causes a wide range of health effects. New data from Seveso found
increased deaths from digestive cancer among women in Seveso who lived closest to the area
that was highly contaminated with dioxin. In a 15-year follow-up study reported in the
November 1997 issue of the journal Epidemiology, Pier Alberto Bertazzi, University of
Milan, and co-authors found that men in the most highly contaminated site had increased
mortality from rectal cancer.
In February 1997 the International Agency for Research on Cancer, a part of the World
Health Organisation, classified TCDD as a Class 1 Human Carcinogen.
It is now recognised that exposure to even minute doses poses damage to health other
than cancer. The United States Environmental Protection Agency (EPA) has conducted a
reassessment of the environmental and human health risks from exposure to dioxin. It is
expected to conclude that exposure to dioxin poses a large scale, long term threat to
public health and the environment -- due not only to increased cancers but also because of
possible birth defects, reproductive problems, nervous and brain disorders and damage to
immune systems.
Q. Are Dioxins produced naturally in the environment?
A. After an extremely extensive review, the U.S. Environmental Protection Agency
(EPA) estimates that 98 percent of dioxins in the environment arise from human
activities.(1) As shown by the historical record of lake sediment cores in the U.S.,
dioxins and furans were almost undetectable until around 1940. Over the following 30
years, their concentrations increased in parallel with increasing commercial production of
organochlorines.(2) Likewise, in archived British soils, concentrations of dioxins and
furans were extremely low during the mid-1880s, then began a steady increase around the
turn of the century, (3) when mass production of elemental chlorine began in the U.K.(4)
The increased use of coal during the industrial revolution was also not responsible:
Studies of atmospheric emission from coal-burning power plants did not detect any PCDD/Fs
(5)
Analyses of ancient human tissues also show that, if dioxins are produced in nature,
the quantity produced is minuscule in comparison to that produced through human
activities. Mummified remains of nine Chilean Indians dating from some 2800 years ago were
found to carry no detectable concentrations of dioxins, with the exception of
octachlorodibenzo-p-dioxin, which was present at concentrations more than 20 times lower
than the lowest values found in people from modern industrialized countries.(6) Similar
results were obtained from the tissues of Eskimos who died and were frozen years ago.(7,8)
| References |
| (1) U.S. Environmental Protection Agency.
"Estimating Exposure to Dioxin-Like Compounds. Volume II: Properties, Sources,
Occurrence and Background Exposures." Review Draft. EPA/600/6-88/005Cb. Washington,
D.C. June 1994. (2) Czuczwa, J.M., McVeety, and B.D., Hites, R.A. Polchlorinated
dibenzo-p-dioxins and dibenzofurans in sediments from Siskiwit Lake, Isle Royale. Science
226 (1984); Czuczwa, J.M., and Hites, R.A. Airborne dioxins and dibenzofurans: Sources and
fates. Environ. Sci. Technol. 20: 195-200 (1986).
(3) Kjeller, L.-O., Jones, K.C., Johnston, A.E., and Rappe, C. Increases in the
polychlorinated dibenzo-p-dioxin and -furan content of soils and vegetation since the
1840s. Environ. Sci. Technol. 25(9): 1619-1627 (1991)
(4) Salzberg, Hugh W., "From Caveman to Chemist: Circumstances and
Achievements," Washington, D.C.: American Chemical Society, 1991.
(5) USEPA (1987). National Dioxin Study Tier 4: combustion Sources: Engineering
Analysis Report. Washington: U.S. EPA Office of Air Quality Planning and Standards,
EPA/450-84-014h; and Fiedler, H., Hutzinger, O & Timms, C.W. (1990). Dioxins: sources
of environmental load and human exposure. Toxicol. & Environ. Chem. 29:157-234.
(6) Ligon, W.F., Dorn, S., and May R. Chlorodibenzofuran and Chlorodibenzo-p-dioxin
levels in Chilean mummies dated to about 2800 years before the present. Environ. Sci.
Technol. 23(10): 1286-1290 (1989).
(7) Schecter, A., Dekin A., Weerashinghe, N., Arghestani, S., and Gross, M. Sources of
dioxins in the environment: a study of PCDDs and PCDFs in ancient, frozen Eskimo tissue.
Chemosphere 17(4): 627-6323 (1988)
(8) Tong, H., Gross, M., Schecter, A., Monson, S., Dekin, A. Sources of dioxins in the
environment: second stage study of PCDD/Fs in ancient human tissue and environmental
samples. Chemosphere 20(7-9): 987-992 (1990). |
Q. Aren't there many different sources of dioxin? Why blame the
chlorine industry?
A. The production of dioxin is inherently linked to chlorine chemistry which is why
the chlorine industry attempts to divert responsibility away from its products and
processes.
In 1980 the Dow Chemical Corporation published a theory called the "Trace
Chemistries of Fire." This was predicated because in the late 1970's, attention
turned to dioxin pollution because of the spraying of chlorinated herbicides and the
effects of dioxin on Vietnam veterans exposed to it as a contaminant in the herbicide
Agent Orange. Producers of chlorinated herbicides faced the possibility of restrictions on
their products and massive class-action claims for health effects among exposed veterans.
At the height of this activity, Dow Chemical, who had been the largest producer of Agent
Orange, published a novel theory in the prominent scientific magazine Science. Dioxin, Dow
said, is a natural chemical, occurring in any and all combustion processes, including
forest fires, volcanoes, and household stoves.[1] Dow's conclusion: dioxin is not a
pollutant uniquely associated with the modern chemical industry but has in fact been with
us "since the advent of fire."[2]
In support of this "Trace Chemistries of Fire" theory, Dow's scientists cited
data that dioxins are ubiquitous in soils, sediments and the residues from many types of
incinerators, including those at its own chemical plants. Perhaps, Dow suggested, dioxin
is formed from the presence of salt -- which is everywhere -- in any type of fire. Dow's
implication was that "natural sources" were and always had been more important
dioxin sources than the chemical industry.
To this day, Dow and its allies repeat the claim of "natural dioxin."
Responding to concern raised by EPA's 1995 dioxin reassessment, for instance, the Chlorine
Chemistry Council emphasized the importance of volcanoes and forest fires as dioxin
sources. A lengthy technical report prepared for the Chlorine Chemistry Council (CCC) by
the American Society of Mechanical Engineers, purported to find that dioxin is formed in
any and all combustion devices irrespective of the presence of chlorinated chemical
products.[3]
A study by Dow in Europe argued that there was no relationship between dioxin emissions
from a German trash incinerator and the feed of chlorinated wastes to the facility. [4]
CCC submitted both documents to EPA as continuing proof of the "trace chemistries
of fire" theory.
This was repeated again in a 1994 Chlorine Chemistry Council and Chemical
Manufacturers Association report "Dioxin Reassessment Briefing Packet"
dioxins are produced naturally and therefore found everywhere in the environment. They
state: "Among the natural sources of dioxin are forest fires, Volcanoes, and compost
piles. Man-made sources of dioxin include municipal, hospital and hazardous waste
incinerators, motor vehicles, residential wood burning and a variety of chemical
manufacturing processes. With so many sources, it is not surprising that scientists have
detected dioxins virtually everywhere they have looked. "
Dioxin synthesis requires four things:
- A source of chlorine (or bromine);
- Organic matter;
- A thermally or chemically reactive environment in which these materials can combine;
- A source of oxygen.
The production of dioxin is inherently linked to chlorine chemistry. Because organic
matter is ubiquitous and reactive environments (such as fires and industrial processes)
are common, it is the presence of available chlorine that is the unique and preventable
factor in dioxin generation. It is only because chlorine chemistry and its products have
become so widespread that dioxin formation appears to be ubiquitous.
The major dioxin sources are those central to chlorine chemistry. For instance, pulp
and paper mills form and release dioxin when they use chlorine gas and other chlorinated
chemicals to bleach wood pulp white. Dioxin is formed in chemical plants when a wide range
of chlorinated organic chemicals are manufactured -- including pesticides, solvents,
chemical intermediates, and feedstocks for the plastic polyvinyl chloride (PVC). Dioxin
has even been identified at the root of chlorine chemistry: in the sludges and residues
from the chlor-alkali process, in which chlorine gas is produced by passing a powerful
electric current through salt-water.[5,6]
Even for those sources not obviously related to the chlorine industry, the presence of
available chlorine turns otherwise dioxin-free processes into dioxin sources.
For instance:
- Automobiles are sources of dioxin because chlorinated chemicals are deliberately added
to fuels; vehicles burning chlorine-free fuels do not emit dioxins.[7]
- Steel mills emit dioxin because chlorinated solvents, cutting oils and plastics are
introduced into these high-temperature furnaces.[8]
- Recycling smelters for copper, lead, and steel are major dioxin sources because the
products recycled in them contain significant quantities of PVC (cable coatings, battery
casings, automobile components, and so on)[9].
- Dioxin is found at sawmills because of the use pentachlorophenol as a wood
preservative[10]
Dioxin is ubiquitous, but only because chlorine chemistry itself has become ubiquitous
in the last 50 years.
What about the largest dioxin sources, incinerators? Incinerators are a major dioxin
source because they burn huge quantities of chlorine-containing wastes.
- Hospital waste incinerators burn huge quantities of PVC plastic -- which accounts for
almost 10 percent of all medical waste.[11]
- Trash incinerators generate dioxin because of the presence of disposable PVC plastic
products, which accounts for about 80 percent or more of the organically-bound chlorine in
the waste stream; chlorine-bleached paper and chlorine-containing household chemicals like
paints, pesticides, and cleaners provide the remainder.[12]
- Hazardous waste incinerators emit dioxin because they burn chlorinated solvents or
copious wastes from the manufacture of chlorinated plastics, pesticides, and other
chemicals.
A host of studies indicate a clear relationship between the burning of chlorinated
organic chemical products and wastes, especially PVC, and dioxin emissions from combustion
facilities.[13,14,15,16,17,18,19,20]
Similarly, dioxin released from forest fires and wood burning are probably due to
contamination of the wood by phenoxyherbicides[16]) or from resuspended material from
aerial deposits[18]
| References |
| (1) Bumb R.R. et al. Trace chemistries of fire: a source of chlorinated
dioxins. Science 210 (4468):385-390, 1980. CCC Executive Newsline. April 3, 1995. 3:12,
page 1. Available from the CCC, 202-887-5412 (2)Crummett W.B. quoted in Chemical
Engineering News 57(7):23-29, 1979
(3) Rigo H., Chandler A., and Lanier W. The Relationship between Chlorine in Waste
Streams and Dioxin Emissions from Combustors Washington: American Society of Mechanical
Engineers for the Chlorine Chemistry Council, 1995
(4) Mark F. Energy recovery through co-combustion of mixed plastics waste and municipal
solid waste. Hamburg: Association of Plastics Manufacturers in Europe, 1994
(5) Rappe, C., et al. Levels, profile and pattern of PCDDs and PCDFs in samples related
to the production and use of chlorine. Chemosphere 23:1629-1636, 1991.
(6) Andersson, P., et al. Analys av Polyklorerade Dibensofuraner och Polyklorerade
Dibensodioxiner i Processprover fran Hydro Plast AB. University of Umea, Sweden, 1993.
(7) Marklund S., et al. Emissions of PCDDs and PCDFs in gasoline and diesel fueled
cars. Chemosphere 20:553-561, 1990.
(8) Lahl U. Sintering plants of steel industry: the most important thermal PCDD/F
source in industrial regions? 13th International Symposium on Chlorinated Dioxins and
Related Compounds. Organohalogens 11:311-314, 1993
(9) Aittola, J et al., (1993) Measurements of Organochloro Compounds at a Metal
Reclamation Plant, Chemosphere 27, 1993, pages 65-72.
(10) Fiedler, H., Hutzinger, O & Timms, C.W. (1990). Dioxins: sources of
environmental load and human exposure. Toxicol. & Environ. Chem. 29:157-234.
(11) Marrack D. "Hospital Red Bag Waste: An Assessment and Management
Recommendations," JAPCA 38: 1309-1311, 1988.
(12) (Danish EPA 1993) Miljoministeriet Miljostyrelsen (Danish EPA), PVC and
Alternative Materials, (English translation) Copenhagen, 1993.
(13) Liberti A., et al. PCDD and PCDF formation in the combustion of vegetable wastes.
Chemosphere 12: 661-663, 1983.
(14) Mahle N. and Whiting L. Formation of chlorodibenzodioxins by air oxidation and
chlorination of bituminous coal. Chemosphere 9:693-699, 1980.
(15) Wagner, J. and Green, A. Correlation of chlorinated organic compound emissions
from incineration with chlorinated organic input. Chemosphere 26(11): 2039-2054, 1993.
(16) Thiesen, J., et al. Untersuchung der Moglichen Umweltgefahrdung Beim Brand Von
Kunststoffen (Investigation of Possible Environmental Dangers Caused by Burning Plastics).
Berlin: Society for Workplace Analysis for German Umweltbundesamt 104-09222, 1991.
(17) Danish EPA 1993, op.cit.
(18) Kanters J. and Louw R. Final report of the RUL-VROM project: GFT, PVC,
Afvalverbranding en 'Dioxine' (Green Waste Fraction, PVC, Waste Incineration and
'Dioxins'). Leiden: Centre for Chemistry and the Environment. Department of Chemistry,
University of Leiden, report number CCESRS 93-09, 1993.
(19) Kopponen P., et al. Comparison of cytochrome P4501A1 induction with the chemical
composition of fly ash from combustion of chlorine containing material. Chemosphere
24:391-401, 1992.
(20) Christmann, W. Combustion of polyvinyl chloride - an important source for the
formation of PCDD/PCDF. Chemosphere 19:387-392, 1989.
(21) Schaum, J., Cleverly, D., Lorber, M., Phillips, L. and Schwarz,G.(1993). Sources
of Dioxin-Like Compounds and Background exposure levels. 13th International Symposium on
Chlorinated Dioxins and Related Compounds. Organohalogens 14: 319-326 |
Q. In some countries, dioxin levels are falling in the environment and
in human breast milk which shows we now have better control over emissions. Why still call
for a phase out of chlorine production?
A. The decrease in dioxin levels in some countries probably reflects the reduction
of some organochlorine pesticides and the shutting down of the worst incinerators. Such
effects are notably seen in Germany and the UK. However such decreases do not pertain
globally. The chlorine industry is expanding in other areas of the world thus increasing
the amount of chlorinated wastes and products which eventually have to be disposed of. It
is now known that dioxins and other persistent organic pollutants (POPS) are carried on
global air currents and distill out in colder latitudes. An increase in production
elsewhere affects us all.
There is no safe dose of dioxin exposure and children are at most risk. End of pipe
pollution control cannot solve the problem of eventual release into the environment.
Better incinerator design, for example, simply reduces atmospheric emissions and diverts
the dioxins generated in the combustion process into contaminated ash residues or aqueous
discharges. In effect, the total quantity of dioxins and furans generated by these
incinerators is more than six times greater than the amount they release into the air.
Currently defined best available techniques such as modern carbon injection systems do not
prevent the formation of dioxins.
These residues are then landfilled or, in some countries, like the Netherlands are used
in road construction. Dioxin is highly persistent, however, and will eventually leak into
the environment where it presents itself for ingestion by animals and thereby intensifies
up the food chain.
Even if the chlorine industry could achieve better efficiency in their production
processes, such as cleaner PVC manufacturing plants, it is impossible to achieve zero
emissions of dioxins and dioxin-like compounds. For instance, highly chlorinated wastes
are always produced during PVC plastic manufacturing presenting risks to workers and
communities. All products of the chlorine industry, particularly PVC plastic, can be a
major dioxin source if accidentally burned in building fires or in smoldering landfills.
Eventually chlorinated products come to the end of their lifecycle and have to be
disposed of. For this reason the chlorine industry avidly supports incineration which
brings us full-circle to the fact that incineration cannot destroy dioxins and other
dioxin-like compounds. It is wiser to simply substitute non-chlorinated processes and
products and move to safer materials.
Q. Can I lower my exposure to dioxin?
A. All industrialized populations carry body burdens of dioxins even vegetarians
and vegans who eat lowest on the food chain. Consumption of organic and less contaminated
food sources, will of course, lessen body burden levels. However this is not a solution.
Dioxins are persistent with a half life in the human body of approximately 7 years. This
means that 50% of dioxin levels will remain after seven years assuming no new inputs
whatsoever an impossibility concerning the global nature and movement of persistent
organic compounds. All evidence now suggests there is no safe dose of dioxin exposure and
that timing of exposure particularly to the developing fetus may be more
important than the quantity of dose. Furthermore, many indigenous human populations, such
as the Arctic Inuit, rely on wild food that continues to be seriously contaminated via
long-range transport of persistent organic pollutants. Other species and their young,
particularly wildlife high on the food web such as marine mammals, have no protection from
environmental contaminants. We have always been an integral part of our global
environment. The continued expansion of toxic industries affects us all.
Q. How are natural estrogens in our food different from synthetic
estrogens?
A. There are major differences between phytoestrogens and man-made
endocrine-disrupting chemicals. Phytoestrogens are readily broken down and excreted from
the body. Consequently they spend very little time inside the body. The situation with
man-made chemicals is different. Humans and animals have not evolved alongside vast
quantities of man-made endocrine-disrupting chemicals in the environment. Unlike
phytoestrogens, many are persistent and cannot be broken down or detoxified. These may
bioaccumulate in body fat, remaining in the body for long periods of time
About 300 different plants are known to produce and contain a number of natural
chemicals called phytoestrogens. These are thought to serve a variety of functions, acting
as natural fungicides, regulating plant hormones, deterring herbivores from eating them
and as a protection against ultraviolet radiation from the sun. Plants that contain
phytoestrogens include many in our diet, such as whole cereal grains, seeds, soy, cabbage,
beet, broccoli and peas. When some phytoestrogens are eaten, they are broken down in the
gut to form estrogen-like compounds, which are able to bind to estrogen receptors.
Phytoestrogens spend relatively little time in the body before being excreted.
Eating a variety of plants in a normal diet does not seem to affect human fertility and
may in fact be beneficial. The most likely explanation is that, as humans and animals have
evolved alongside plants, any harmful effects on fertility that a normal diet may cause,
may have been selectively bred out of the populations long ago. |