Environment
April/May 1975
Fluoride Pollution
by Edward Groth III
EDWARD GROTH III is a staff officer, Environmental Studies Board,
Commission on Natural Resources, National Research Council, Washington,
D.C ENVIRONMENTAL CONTAMINATION by fluorides exposes many
organisms to potentially toxic effects and may exert some stress
on the ecological interrelationships among plant and animal populations
in natural biological communities. Research to date has focused
on human beings and species important to humans; (1) relatively
little is known of the potential ecological consequences of fluoride
pollution. This article presents a literature review of what is
known about the ecological effects.
In brief, the available data fall short of providing conclusive
proof that any major, significant, or irreversible ecological changes
have occurred, or are likeIy to occur, as a result of existing levels
of fluoride pollution. (In this context, ecological effects means
changes in the balance of natural ecosystems, not the very severe
damage to commercial timber crops and livestock that has occurred
because of fluoride pollution. See, for example, "Fluorides in the Air,"
Environment, April 1973.) Nevertheless, the available evidence does
support the view that fluorides are pollutants with considerable
potential for producing ecological damage. The compounds are potentially
serious contaminants not only when present in highly localized,
massive concentrations, but also when distributed in low-level amounts
over a long period of time. As future research begins to bring potential
ecological impacts of fluoride into better focus, it seems very
likely that proof will develop that the ecosystem does suffer damage
when fluoride levels of the magnitude discussed here are present.
The evidence which supports concern over potential ecological impacts
of low-level fluoride pollution can be summarized as follows:
* Levels of fluoride air pollution capable of leading to significant
accumulation in vegetation and consequent injury to some sensitive
plants have occurred several miles or more from sources of fluoride
emissions, despite air pollution controls.
* Significant fluoride accumulation has been demonstrated in insects
and in birds and mammals that feed on plants in the vicinity of
pollution sources. The accumulated levels have been high enough,
in some cases, to be potentially toxic, and such buildup represents
a major increase of fluoride in food chains.
* Water pollution from both industrial sources and municipal sewage
seems capable of producing downstream concentrations of 0.5 to 3
parts per million (ppm). Concentrations are highest during summer
months, when biological activity is also at its peak. Some reports
of toxic effects in algae and freshwater vertebrates at 1 to 2 ppm
fluoride have been published. Most invertebrate species studied
can accumulate significant bodily burdens of fluoride at this level
of pollution, and there are indications that aquatic vegetation
may also concentrate the element. It seems very likely that fluoride
is accumulating, and probably being magnified, along aquatic food
chains.
* Substantial amounts of fluoride are transferred to the soil each
year. The degree to which this fluoride is available for uptake
by soil organisms, and the extent to which soil life may be affected
by fluoride in the environment, remain unknown.
* Possible conversion of fluoride into fluoroacetate (more toxic
than fluoride itself and related organic forms), and the likelihood
that fluoride may enter into synergistic actions with other contaminants,
greatly expand the potential for ecological damage by low-level
fluoride contamination.
Fluoride Air Pollution
Estimates by the National Research Council and the Environmental
Protection Agency (3) suggest that between 120,000 and 155,000 tons
of fluoride (calculated as hydrogen fluoride) are emitted into the
atmosphere each year in the U.S. Fluoride is released from a variety
of sources including aluminum smelting and phosphate processing
operations; the combustion of coal; and the manufacture of steel,
brick, tile, clay, and glass products. Reductions in fluoride emissions
with increasing application of control regulations may be offset
by the rapid growth of some fluoride sources, particularly phosphate
fertilizer and aluminum production.
Most major fluoride sources use wet scrubbers to remove the pollutant
from exhaust streams. Such controls are essential because concentrations
as low as one part per billion (ppb) in ambient air are capable
of causing serious damage to vegetation and may threaten livestock.(2)
Concentrations of 10 ppb or higher have been measured in the immediate
vicinity of a source, (4) and fluoride levels in the 1 ppb range
may occur for several miles downwind of an emission point. In general,
however, except downwind of a source, or in urban areas where many
sources are present, the air rarely contains measurable fluorides.
Environmental Effects
According to a review by the US Department of Agriculture, fluorides
have done more damage to livestock, worldwide, than any other air
pollutant. (6) Some plants, including several important timber varieties
of coniferous trees, are sensitive to fluoride damage. (2) Concentrations
of 1.0 ppb or less can lead to long-term environmental damage because
of biological magnification (the significant increases in pollutant
concentrations which occur at each successively higher level in
a food chain).(7) Some forage grasses can accumulate 200,000 times
the level of fluoride present in the surrounding air. (2) Prolonged
ingestion of contaminated forage by livestock can lead to excessive
accumulation of fluoride in the bones which may, in turn, produce
skeletal deformities and other damage to the animals' health. (6)
Several studies in the past five years have begun to explore potential
effects of fluoride on natural vegetation and wildlife species not
previously investigated. For example, when samples of lichens and
mosses were exposed to pollution from an aluminum smelter in Quebec
in four- or twelve-month studies at distances of from about one-half
to nine miles downwind of the source, the lichens showed severe
fluoride injury symptoms, especially near the source, and both lichens
and mosses accumulated the pollutant. Lichens, exposed for four
months about one-half mile from the source had 990 ppm, mosses,
570 ppm Even samples nine miles from the source showed 190 ppm (lichens,
at four months) and 78 ppm (mosses, at twelve months). (8) Similar
accounts of the effects of fluorides on lichens in Pennsylvania
and Scotland have been published. (9)
Several scientific groups in Montana recently investigated the effects
of fluoride on a wide range of plants and animals exposed to the
contaminant. The polluted areas studied were near the Anaconda Aluminum
Company smelter in Columbia Falls and the Rocky Mountain Phosphate
Company plant in Garrison. Despite pollution control measures employed
by both companies (reported to be 99 percent efficient in controlling
fluoride emissions), fluoride contaminated the environment and accumulated
in a large number of organisms.
Vegetation in a 400-square-mile area downwind of the Columbia Falls
aluminum smelter accumulated significantly elevated levels of fluoride
(more than 10 ppm); on more than one-quarter of that area, foliage
levels exceeded 30 ppm (10) Several species of pines, firs, grasses,
hay, and a large number of of shrubs and herbs were sampled, and
many were found to contain significant amounts of fluoride, even
at distances of more than twenty miles from the source. Insects
of several dozen species were captured in the polluted area, and
almost all samples had high levels of fluoride. Control samples,
taken from a nonpolluted area, showed fluoride levels of 3.5 to
16.5 ppm in their tissues while insects from the study area had
6.1 to 585 ppm. Insects from the pollinator group (such as bees)
generally had the highest fluoride levels. Some species that are
predatory throughout their life cycles had an elevated fluoride
content, suggesting the transfer of the pollutant through the food
chain. (11)
University of Montana investigators analyzed the thigh bones of
more than 300 animals taken from different parts of the study area.
They found that skeletal fluoride accumulation was 10 to 40 times
higher than that in animals taken from nonpolluted areas. Many of
the chipmunks, ground squirrels, and other mammals and birds in
the sample had bone fluoride levels in excess of 1,000 ppm, and
several individual animals had concentrations of from 5,000 to 13,333
ppm (12)
The investigation of the area around the Garrison phosphate operation
revealed a similar, although geographically more limited, pattern.
The fluoride levels of many samples of vegetation exceeded the 35
ppm state standard, some samples contained more than 100 ppm. Animal
specimens had above normal accumulations which correlated well with
the concentrations in plants at the sites where the animals were
trapped. (13)
A similar study showed significantly elevated fluoride levels in
grass, and in bones of sparrows and frogs near an aluminum smelter
in Czechoslovakia. (14) In general, however, few other data have
been gathered on the potential impact of fluoride pollution on wildlife
species.
Although the data available to date are few, they fit a pattern.
The ability to accumulate fluoride from very low ambient air concentrations,
and to build up levels of 10 to 100 ppm or more appears to be very
widespread among different kinds of vegetation. A broad range of
herbivorous (plant-eating) animals in polluted regions, sometimes
many miles from the source of pollution, seem to be accumulating
substantial fluoride, primarily through their diet. Levels in animals
are generally higher relative to control sample levels than levels
in plants, reflecting the magnified effects which occur as a pollutant
moves up the food chain. Since very few samples of predatory animals
have been analyzed, no solid conclusions can be drawn about the
potential hazards to animals higher in food chains. However, experience
with other food chain pollutants (for example, DDT) indicates that
predators are often hardest hit by cumulative contaminants. It seems
urgent, therefore, to obtain further data on fluoride accumulation
in predatory species.
Fluoride Toxicity
The potential biological and ecological significance of fluoride
accumulation, as reported in these studies, is not easy to evaluate.
In general, there is little information available on the toxicity
of fluoride to most wildlife species. Data on domestic plants and
livestock indicate wide differences in the sensitivity, of various
species to fluoride injury. (5) Some conifers are among the most
sensitive plant varieties. Investigators in Montana reported that
pines, especially the western white pine, were dying out over hundreds
of acres near the aluminum plant in their study. They concluded
that loss of the pine trees was altering the normal ecological succession
of the forest community at those sites and could lead to major changes
in the vegetation patterns of the area. (16) It is not known whether
fluoride may be having injurious effects on other important members
of the plant community in the polluted areas, but should such effects
occur, they would alter not only the balance of vegetative types,
but of animals as well.
Extensive studies on domestic animals indicate that 30 to 40 ppm
fluoride in forage can be seriously toxic to cattle when ingested
on a prolonged basis, and that sheep, swine, and other species seem
to be able to tolerate higher amounts of fluoride in their feed.(6)
Data on herbivorous wildlife species are not available, but it should
be assumed, in the absence of contrary information, that fluoride
levels of 30 ppm or more found in large areas in Montana may represent
a hazard to animals which habitually feed on the contaminated vegetation.
In domestic cattle, skeletal concentrations ranging from 1,450 to
over 8,000 ppm have been associated with fluorosis (fluoride poisoning),
and bones from a horse injured by fluoride pollution had 1,060 to
1,500 ppm (6) Although no direct relationship was established between
skeletal fluoride accumulation and health effects in the animals
in Montana, it seems logical that at least those animals in which
skeletal fluoride exceeded 5,000 ppm could have suffered some adverse
health impact.
Some information on fluoride toxicity to insects is available. Mulberry
leaves containing 10 to 15 ppm fluoride were lethal to silkworm
larvae, while leaves containing lower fluoride levels led to reduced
growth of the insects. (17) In other studies, (18) sodium fluoride
added to flour affected the survival and reproduction of the flour
beetle, Tribolium confusum; some concentrations appeared
to inhibit, and others to enhance, egg production. Considerable
evidence is available to indicate that honeybees are highly sensitive
to fluoride. Bee colonies in the vicinity of fluoride sources have
frequently been heavily damaged. Two of the Montana investigators
commented that the highest accumulation of fluoride among insects
in their study was in members of the pollinator group. (16) They
speculated that if other pollinators should prove as susceptible
to fluoride injury as the honeybee, patterns of pollination in a
polluted region could be substantially altered; and, as a consequence,
the abundance of many insect-pollinated plants could shift, with
attendant major changes in the ecology of an entire community.
It must be emphasized that research to date has not probed for such
ecological effects, and we cannot say that they are occurring in
the vicinity of fluoride air pollution sources. Nevertheless, the
potential for such effects seems real enough, making this an area
in which more research would be desirable.
Water Pollution Sources
While fluoride air pollution primarily occurs in the vicinity industrial
sources, fluoride is released into the aquatic environment by a
far wider range of sources, and it seems very likely that most bodies
of water are contaminated by fluoride to some extent. Some fluoride
is present in waters from natural sources. Many minerals contain
soluble fluoride, and when ground water passes through such fluoride-bearing
rock formations, the water may become contaminated. A few sources,
primarily deep wells, contain 1 ppm fluoride or more. Most surface
waters contain less than 0.2 ppm fluoride, and the majority are
below 0.1 ppm (19) The oceans, as the result of eons of leaching
of mineral salts from the land, contain from 1.2 to 1.4 ppm fluoride,
about half in the form of fluoride ion and half in the relatively
insoluble, magnesium fluoride complex ion. (20) Although natural,
or "background," fluoride levels in most fresh-water streams
are in the 0 to 0.2 ppm range, available data indicate that concentrations
above 0.5 ppm, and occasionally as high as 2 or 3 ppm, may be fairly
common in watercourses contaminated by human activities.
Several human activities result in substantial fluoride input to
the aquatic environment. Many of the industries which have fluoride
air pollution problems are also sources of fluoride water pollution.
Air pollution control equipment often produces a fluoride laden
liquid waste which requires disposal. (Fluoride can be removed from
wastewater by treatment with lime in settling ponds, a form of treatment
which can reduce the fluoride content of an effluent stream from
more than 5,000 ppm to about 5 to 50 ppm) (21) Aggregate figures
for all fluoride sources are not available, but the phosphate industry
may discharge from 6,000 to 30,000 tons of fluoride into waterways
in the US annually.(22) The Environmental Protection Agency has
proposed standards for the primary aluminum industry which, starting
in 1977, would restrict fluoride in wastewater discharge to an average
of two pounds per ton of aluminum produced. If all aluminum smelters
were currently meeting that standard, fluoride discharges would
be 4,000 to 5,000 tons per year from this industry. However, only
about one-third of the plants now in operation are presently in
compliance, so actual fluoride pollution from the aluminum industry
is probably substantially larger. (23) Fluoride discharges from
other industries are not negligible, but are probably smaller than
from phosphate and aluminum operations.
Another significant source of fluoride water pollution is domestic
sewage. Approximately one-half of the communities in the US which
have centralized water distribution systems now add fluoride to
their water supplies for the partial control of tooth decay. (24)
Provision of fluoridated water for 100 million people requires the
addition of approximately 20,000 tons of fluoride to domestic water
supplies each year. Most of the water used in urban areas, and thus
most of the fluoride added to water supplies, is returned through
sewage systems to the aquatic environment.
A study of fluoride levels in sewage in 56 California cities demonstrated
that domestic sewage already contains fluoride, over and above that
naturally present in water or added for dental health. (26) Fluoride
in human wastes, originating with fluoride in foods, was tentatively
identified as the source of the excess. The investigator concluded
that fluoride from toothpastes and other sources would make a negligible
contribution, and that no industrial sources were contributing fluoride
to the sewage samples studied. The findings suggest that the total
input of fluoride into the environment from domestic sewage is probably
more than the 20,000 tons estimated to be added to water supplies
in communities where fluoridation of drinking water takes place.
Thus, even communities not fluoridating water may release significant
fluoride into receiving streams in their sewage.
The same study showed that secondary sewage treatment (biological
digestion of wastes) reduced fluoride in the final effluent by an
average of 57 percent, while primary treatment had no appreciable
effect on fluoride levels. Even with secondary sewage treatment,
however, it was concluded that significant amounts of fluoride persisted
in effluents.
Fluoride is present in phosphate fertilizers, and some fluoride
may be carried into surface waters in runoff from agricultural lands.
It is also likey that some portion of fluorides emitted into the
air is eventually carried by precipitation into surface waters.
(27) While these sources may be significant, good quantitative estimates
of the magnitude of fluoride input to the aquatic environment by
these routes are not available.
Environmental Concentrations
Although fluoride air pollution leads to significant environmental
concentrations only in the vicinity of sources, low-level fluoride
water pollution appears to be more widespread.
The US Geological Survey monitors water quality at several thousand
sites around the country, but fluoride data are not routinely included
in chemical analyses. Fluoride readings for some streams are available,
however. Many rivers have fluoride contents ranging from 0 to 0.2
ppm, but some have much higher levels. For example, 1967 data for
the Santa Ana River in California showed fluoride levels of 0.9
to 3.6 ppm (average, 1.1 ppm), and single readings in the Pit River
(also in California) reached 1.8 and 2.1 ppm (28) (Earlier monitoring
at the same sites on the Pit River recorded levels of 0.1 to 0.2
ppm) (29)
A number of published studies relate environmental fluoride concentrations
to specific sources of the contaminant. Tributaries of the East
Gallatin River above the town of Bozeman, Montana, contain 0.1 ppm
fluoride or less, while the river below the city's sewage outfall
(the only fluoride source in the area) has been found to have concentrations
of 0.3 to 0.8 ppm (30)
Fluoride concentrations of from 0.17 to 2.06 ppm were measured in
a study of the Illinois River. (31) The highest concentrations occurred
during the summer months, when stream volume was lowest. Fluoride
sources upstream from the monitoring site included several communities
with fluoridated water supplies and several major fertilizer manufacturing
plants. A study of fluoride input to Narragansett Bay, in Rhode
Island, showed that 36 percent of the fluoride entering the bay
was due to fluoridation of water supplies in five communities on
rivers feeding into the estuary. (32) In midsummer, pollution from
these sources was enough to double the fluoride content of the rivers.
A similar study in Japan showed fluoride concentrations of 0.15
to 1.07 ppm in rivers feeding into Tokyo Bay. (33)
Pollution near industrial sources, especially where only limited
wastewater treatment to remove fluoride is employed, can be much
more serious. Concentrations of 20 ppm or more were reported for
the Pamlico River (in North Carolina) near a phosphate plant. (34)
In most states where industrial fluoride discharge is a problem,
relevant water quality standards have been adopted. Standards for
drinking water sources generally are based on the US Public Health
Service Drinking Water Standards and prohibit concentrations in
excess of 1.5 to 2.0 ppm Some states permit levels of 5 to 10 ppm
for bodies of water which are not sources of public water supplies
in order to prevent toxic effects to wildlife. (35)
Ecological Effects
The critical question for biologists is whether chronic exposure
to these fluoride concentrations, which may be from two to ten or
more times higher than the background level, poses any significant
physiological or ecological hazard to aquatic life. It seems reasonable
to conclude that fluoride at these levels poses no major risk to
marine organisms. (32) Both the dilution factor, and the fact that
most oceanic forms evolved in an environment that contains from
0.6 to 0.7 ppm fluoride ion, suggest that potential effects on marine
life should be minimal if fluoride in rivers rarely exceeds 2 ppm
However, freshwater organisms evolved in an environment that was
almost fluoride-free, and thus might be expected to be less well-equipped
to tolerate fluoride concentrations encountered in polluted streams.
Relatively little is known about the potential impact of fluoride
on either freshwater or marine organisms. A number of investigators
have measured the short-term toxicity of various fluoride compounds
for a good number of species, but systematic inquiries on the more
general effects of long-term, low-level pollution, analagous to
the Montana air pollution studies discussed above, have rarely been
published. Thus, we may know the lethal concentrations for many
organisms, but we have very little knowledge of the sublethal effects
of fluoride on behavior or reproductive processes, or of potential
accumulation of the pollutant in aquatic food chains. Yet such effects,
should they occur, would probably be more important ecologically
than the mortality which might result from very high, but short-lived,
pollution episodes. (36)
Several investigators have exposed a variety of bacteria and microscopic
animal species that live in freshwater to a range of fluoride concentrations
extending well above those likely to be encountered in streams,
without any demonstrable toxic effects. (37) Not many species have
yet been tested, however, and the criteria for evaluating toxicity
were not sophisticated. The finding that bacterial digestion of
sewage removes much of the fluoride content of the effluent (26)
suggests that some bacteria may accumulate fluoride from water.
The importance of bacteria as a basic element in food chains makes
it important to learn more about the capacity of microorganisms
to bioconcentrate this contaminant.
The single-celled green alga Chlorella showed a 37 percent
reduction in growth over 48 hours when exposed to a 2 ppm fluoride
solution; (38) 43 ppm was reported lethal to another alga, Scenedesmus.
(39) Few other data on toxicity of fluoride to aquatic plants are
available, but several studies suggest that water plants can accumulate
the element. Five-day exposures to 100 ppm led to a 50-told concentration
of fluoride by aquatic plants, and fourteen days at 20 ppm produced
a 38 fold increase. (27) Water hyacinths absorb fluoride efficiently
at concentrations above 10 ppm, and to a much lesser extent at lower
Ievels. (40) Several species of marine algae (exposed to 0.5 to
0.7 ppm) contained 2 to 22 ppm fluoride. Eel grass and the alga
Cladophora, however, showed no significant fluoride buildup
after seventy-two days in sea water with 52 ppm fluoride. (42) One
Russian study found an average fluoride content of 40.5 ppm in samples
of several freshwater plants, (43) and other studies strongly suggest
that aquatic vegetation accumulates fluoride. (44) However, the
evidence as a whole is still too fragmentary to provide a clear
or systematic picture of the capacity for fluoride buildup in aquatic
plants.
Effects on Aquatic Animals
Short-term fluoride toxicity data are available for a number of
invertebrate species, the majority of them marine varieties. Water
fleas are killed or immobilized by concentrations of various fluoride
compounds ranging from 5 to 500 ppm (45) Lobsters are not harmed
by 5 ppm fluoride. (46) Mussels may be killed by 1.4 to 7.2 ppm,
(42) and concentrations of 20 ppm or higher for extended periods
have been shown to be toxic or lethal to oysters, two species of
crabs, and a sand shrimp, but not to two types of prawns. (47) More
significant than the lethal effects of high concentrations, however,
is the marked ability demonstrated by almost all species studied
in these investigations to accumulate substantial bodily burdens
of fluoride. Even animals kept in sea water containing only 1 ppm
fluoride had bodily concentrations of from 100 to 300 ppm (48) The
entry of fluoride into food chains through bioconcentration in aquatic
invertebrates is a subject in need of much more careful research.
Studies of the effects of fluoride on fish are far more numerous
than for any other form of aquatic life . (49)
Short-term lethal effects may occur at concentrations as low as
3 ppm in sensitive species (for example, rainbow trout), while other
fish are not damaged until fluoride levels reach 100 ppm Water temperature,
hardness, chlorinity, and other environmental factors, as well as
the age and physiological state of the fish, can influence the toxicity
of a given concentration of fluoride. (50)
Sublethal concentrations may have adverse effects on fish behavior
or reproduction, which could be ecologically significant. Research
findings are few and not confirmed, but trout eggs seem to be delayed
in development and hatching by 1.5 ppm fluoride. (51)
Fish are important food-chain organisms, and the ability of many
fish, like many other vertebrates, to accumulate elevated fluoride
levels in their skeletons (52) can introduce the contaminant into
the diet of fish-eating predators. Levels of 550 to 6,800 ppm have
been reported in bones of ocean fish, and 400 to 1,600 ppm in trout
from a naturally high-fluoride stream in Yellowstone National Park.
Such accumulation might pose a hazard to animals that eat whole
fish.
Data on other aquatic vertebrates which may be exposed to fluoride
are sparse. Frogs were killed in one week by 900 ppm fluoride, (53)
and decreased red and white blood cell counts were observed in frogs
kept in fluoride concentrations of 5 to 300 ppm (54) There have
also been indications that sublethal fluoride concentrations may
adversely affect amphibian reproductive cycles. (55) Frog eggs were
retarded in development but hatched prematurely in 1 ppm fluoride
in well water, higher concentrations (13 to 450 ppm) had the same
effects on toad eggs, and metamorphosis in tadpoles was significantly
delayed by fluoride at 0 5 and 4.5ppm. (56)
Most research on the effects of fluoride on aquatic organisms dates
back to the early 1960s or before, and more definitive studies are
required on the potential hazards suggested here. There is also
a pressing need to examine the potential impact of chronic, low-level
bioaccumulation of fluoride on predatory animals higher in aquatic-based
food chains. As is the case with fluoride air pollution, the logic
of ecosystem energy and nutrient flow patterns suggests that species
at the highest levels of a food chain are likely to bear the greatest
risk of harm, but virtually no effort has been made to look for
such damage. If fluoride has had such adverse effects on aquatic
wildlife, they have thus far been too subtle to attract attention.
In the absence of any substantive research data, it would be unwise
to assume that no risks exist.
Soil Pollution Sources
Because fluoride is a common constituent of several relatively abundant
minerals, most soils contain this element. The range for most normal
soils is 100 to 300 ppm, but levels of up to 8,300 ppm have been
found in heavy clay soil. (2) Additional sources of fluoride input
to the soil may be present in many localities. Air pollution can
lead to a substantial increase in soil fluoride content, both through
fallout of particulate fluorides and through the absorption of gaseous
fluorides in rain and snow. (57) Phosphate fertilizers may contain
0.5 to 4.0 percent fluoride by weight as an impurity. One investigator
calculated that fertilizer applications in Germany were adding from
7.0 to 17.6 pounds of fluoride each year per acre of land fertilized.
(58) This compared to 1.8 pounds per acre of fluoride added to the
soils in his study area by air pollution, and to values of 6.1 to
19.2 pounds for each acre input from air pollution in similar studies.
In the US, 5 million tons of phosphate fertilizers were applied
to soils in 1973. (59) If it is assumed that the average fluoride
content of that fertilizer was 2 percent by weight, this represents
an input of 100,000 tons of fluoride to US soils.
Additional fluoride input to soils may occur when fluoride-containing
waters are used in irrigation. No quantitative estimates are available
for the magnitude of such contributions to fluoride contamination
of the soil, however.
Fate of Fluoride in Soils
More than 90 percent of the natural fluoride content of soils is
insoluble, or tightly bound to soil particles. (27) Most soil samples
show lower fluoride content near the surface than at depths of a
few feet, indicating that the soluble fraction of fluoride may be
removed from the surface by water seeping into the ground. It appears,
therefore, that under normal conditions very little fluoride is
available for uptake by plants, even in soils that may be relatively
rich in fluoride.
Research findings differ on the degree to which fluoride added by
pollution or fertilization is available for uptake in the plant
roots. When soluble fluoride compounds (for example, sodium fluoride)
were added to soils in concentrations of 150 ppm or more during
one experiment, significant uptake by plants occurred. (60) Other
experiments showed that a substantial amount of fluoride was removed
from polluted soils by water. (61) On the other hand, it has been
found that as much as 90 percent of fluoride from fertilizers and
air pollution may remain in the soil; (58) another report showed
that some soils, especially those with relatively high calcium content,
were very effective in fixing fluoride, with the result that little
was available for plants to incorporate. (62)
It seems very likely that a number of soil characteristics, as well
as other environmental factors, can have a marked influence on the
availability of fluoride to plants. For example, fluoride is more
readily available in sand or acid soils than in high-clay soils.
(63) Also, a relationship exists between the type of nitrogen fertilizer
applied and the toxicity of fluoride to crops. (64) The use of certain
boron-containing fertilizers leads to a dramatic increase in the
accumulation of fluoride in the leaves of fruit trees. (65)
Biological Effects
The only research on the biological impacts of soils contaminated
by fluoride has dealt with uptake of the chemical by plants. Data
from one study showed that grasses grown in soils containing 1,350
ppm fluoride could contain as much as 1,330 ppm (14) In many similar
reports, it has been observed that when fluoride is present as both
an air pollutant and a soil pollutant, plant uptake from air (through
the tiny openings in leaves where gases are exchanged) is far more
significant than from soil. Several investigators have shown, however.
that substantial uptake can occur from soil alone under some conditions.
(66)
A number of investigators have shown that the uptake of fluoride
pollution from soil can have toxic effects on some plants. For example,
1,000 to 1,500 ppm fluoride added to soil in one experiment reduced
the yield of winter wheat by 40 to 65 percent and 400 ppm reduced
growth of Tradescantia, a flowering plant by 28 to 34 percent;
(60) a strong correlation has been demonstrated between inhibition
of pea seedling growth and increased fluoride content of the soil,
(67) and fluoride concentrations of 1.9 to 190 ppm in soil reduced
the growth of loblolly pine and red maple trees. (68)
The most obvious ecological concerns arising from fluoride pollution
of the soil center around uptake of the contaminant by plants, not
only because of potential toxic effects to the plants themselves,
but also because the process may introduce additional fluoride into
the diets of animals.
But uptake by plants is just a small part of the possible impact
soil fluoride might have on living things. The soil is anything
but a sterile medium; it is, in fact, a very rich, and highly diverse,
ecosystem which includes thousands of species of microbes, fungus,
worms, and insects. (69) Many of these soil organisms are essential
to the fertility of the land - for example, they convert nitrogen
to a form useful to plants, help break down organic matter and by
turning the soil, help aerate it. Disruptions by soil ecology by
toxic pollutants could potentially reduce the land's ability to
support plant life, and thus, all life.
Whether the fluoride now being added to soils in fertilizers and
as fallout from air pollution poses any real threat to the ecological
balance of the soil community cannot be determined yet. There are
virtually no published data on the toxicity of fluoride to soil
organisms, or the potential for accumulation of fluoride in soil
food chains. Until research has been conducted on this subject,
we will have no way of knowing, but the possibility must be considered
that fluoride may be potentially as dangerous to some soil organisms
as it is known to be to some terrestrial and aquatic varieties.
Biosynthesis of Organofluorides
Many environmental contaminants may be altered chemically by the
action of living things, and in this way be transformed into substances
more toxic than the pollutants in their original form. The methylation
of mercury by bacteria is one example of such biotransformation.
(See "Mercury in the Environment," and "Mercury in
Man," Environment, May 1971.) Another is the synthesis of highly
toxic azo compounds from aniline-based herbicides which has been
reported to occur in soil microorganisms. (See "The Soil Transforms,"
Environment, May 1971.) There is convincing evidence now that some
plants can synthesize organic fluoride compounds, primarily fluoroacetate
and fluorocitrate, from inorganic fluorides. Although inorganic
fluorides are themselves quite toxic, fluorocitrate and fluoroacetate
are much more toxic. According to one expert in the field, "Fluoroacetates
and their related compounds...are among the most poisonous substances
known." (70)
The biosynthesis of organofluorides was initially demonstrated in
certain tropical plants noted for their extreme toxicity to livestock.
It has been observed that these plants may contain several hundred
ppm of fluoro-organic compounds in their leaves, but the plants
usually grow in soils which are low in fluoride (11 and 216 ppm).
(71) Fluoroacetate levels of up to 1,100 ppm have been measured
in the leaves of one tropical plant growing in an area where soils
contained 1 to 6 ppm fluoride, and the water only 0.05 ppm No other
plants in the vicinity contained more than 2 ppm fluoride. Some
of the plants that synthesize fluoro-organic compounds, therefore,
appear to have an exceptional ability to extract fluoride from an
environment in which the element is present only in extremely small
traces. (72)
More than two dozen toxic plants are known to be able to synthesize
fluoroacetate, (73) but much interest has been generated by recent
findings, which could be of great ecological importance, that suggest
that the ability to make organic fluoride toxins may be much more
widespread than was previously suspected. Fluoro-organic residues
have been detected in several salad and forage crops.(74) Measurements
have shown 179 ppm fluoroacetate and 896 ppm fluorocitrate in forage
crops grown in fields near a phosphate plant. (75) Soybean plants
exposed to hydrogen fluoride in the laboratory had concentrations
of 40 and 140 ppm of the same two compounds. (76) Other workers
have reported that single-cell cultures of soybeans possess the
ability to synthesize fluoro-organic compounds; (77) lettuce can
convert fluoroacetate to fluorocitrate. (78) At least one attempt
to detect organic fluoride compounds in crop plants exposed to fluoride
was not successful (79) although others have repeatedly confirmed
these findings. (73)
Compared to the amounts of fluoro-organic toxins found in some of
the poisonous tropical plants mentioned above, the quantities detected
in most of the more common plants tested are quite small and may
not be a toxic threat. However, organofluorides have also been reported
in tea and in oatmeal (80) and may be very widespread in both the
human and natural food chains. Recent reports that fluoro-organic
residues are present in the bones of cattle and horses (81) are
suggestive of food-chain transfer. Sodium fluoroacetate, sold commercially
under the name "Compound 1080" is a widely employed rodenticide,
(92) and unintended transfer of the poison through the food chain
has had adverse effects on some predators which feed on rodents.
If increasing fluoride pollution of the environment should lead
to a general buildup of fluoro-organic compounds in natural food
webs, it is possible that the ecological damage which might occur
could be severe.
A great deal of research is needed to determine whether biosynthesis
of organic fluorides does in fact add a serious new dimension to
the potential ecological consequences of fluoride pollution. We
need to know which organisms possess the ability to synthesize these
toxins, and in particular whether such abilities exist in members
of aquatic and soil communities. There is evidence that some soil
microorganisms may synthesize fluoroacetate; (83) the existence
of this capacity in microbes, as well as higher plants, needs to
be explored. Some plants have also been shown to break down organic
fluoride compounds.(84) Some bacteria may also be able to defluorinate
these substances. (71) A great deal of work is still needed to track
the environmental fate of fluoro-organic toxins in natural biological
systems, and to determine the magnitude of any threat arising from
the biosynthesis of such compounds that may occur in a fluoride-contaminated
environment.
Potential Synergisms
It seems likely that fluoride may interact synergistically with
other environmental pollutants to produce greater effects than either
pollutant could cause were it acting alone. One study shows a pronounced
synergistic effect between fluoride and copper which resulted in
the inhibition of cellular respiration in Chlorella. (85)
The influence of boron, contained in certain fertilizers, on fluoride
uptake by plants has been noted above. (65) Other evidence suggests
that there are synergistic effects between hydrogen fluoride and
sulfur dioxide in the air.
Other factors in the environment may also modify, and in some cases
offer protection against, the toxic effects of fluoride. The presence
of some mineral elements, especially calcium, in soil and water
seems to reduce potential fluoride availability and, therefore,
the potential damage. Many other geochemical, physical, and biological
parameters may well influence the effects of a given level of fluoride
on any organism or ecosystem. This complexity, combined with the
lack of solid experimental data, make evaluation of existing toxicological
information all the more difficult.
Conclusions
Although based on still fragmentary research data, the conclusions
summarized at the start of this paper comprise a fairly compelling
case for treating fluorides as pollutants with a great capacity
to do ecological harm. Research to provide a more definitive assessment
of the environmental risks of low-level fluoride pollution is urgently
needed. Priority areas for study should include the following: the
effects of fluoride in food chains, particularly on predators at
the higher levels of trophic webs; the physiological impact of chronic
exposure to fluoride, at concentrations now present in the environment,
on many of the most important species in land, aquatic, and soil
ecosystems; the sublethal toxic effects, such as interference with
reproduction, alteration of behavior, or increased susceptibility
to diseases, predation, or parasitic attack. Data are needed as
well on the effects of fluoride on soil organisms, an area in which
we are virtually completely without information, and better understanding
is needed of the synthesis and transfer of organic fluoride poisons
in ecosystems. In addition, much more complete monitoring to record
levels of fluoride actually present in ecosystems, especially freshwater
streams, would be very useful.
To date, except for instances of gross spillage of fluoride into
the air or water, fluoride has received relatively little attention
as a contaminant of the ecosystem. In the case of water pollution
especially, there have been many other pollutants which have been
present in massive amounts, and which have had a very significant
impact. It is easy to understand how a pollutant like fluoride,
which is usually present at fairly low levels, and which has more
subtle, insidious effects, when it has effects at all, has been
given relatively low priority, both in terms of research attention
and regulatory control. It is possible that fluoride may have had
some adverse effects on aquatic life, but that such damage has been
masked by the far more severe effects of untreated sewage, industrial
effluents, pesticides, and other major pollutants. As controls on
these more easily recognized pollution problems are becoming more
effective and widespread, attention can turn to less prominent pollutants
such as fluoride, whose impacts may be more easily detected as water
quality improves in respect to other parameters.
To learn more about fluoride pollution, click
here.
NOTES 1. National Research Council, Fluorides,
Committee on Biological Effects of Atmospheric Pollutants, National
Academy of Sciences, Washington, DC, 1971. World Health Organization,
Fluorides and Human Health, WHO Monograph No. 59, Geneva, 1970.
2. National Research Council, ibid.
3. US Environmental Protection Agency, Engineering and Cost Effectiveness
Study of Fluoride Emissions Control, Washington, DC, Jan. 1972.
4. Prival, M.J., and F. Fisher, "Fluorides in the Air,"
Environment, 15(3):25-32, 1973. Cross, F.L., and R.W. Ross, "Fluoride
Emissions from Phosphate Processing Plants," Fluoride Quarterly
Reports, 2(2):97-105, 1969.
5. Yunghans, R.S., and T.B. McMullen, "Fluoride Concentrations
Found in NASN Samples of Suspended Particles," Fluoride, 3(3):143-152,
1970.
6. Lillie, R.J., Air Pollutants Affecting the Performance of Domestic
Animals, A Literature Review, Agricultural Handbook No. 380, Agricultural
Research Service, USDA, Washington, DC, 1970.
7. Hill, A.C., "Air Quality Standards for Fluoride Vegetation
Effects," J. Air Poll. Cont. Assoc. , 19(5):331-336, 1969.
8. LeBlanc, F., G. Comeau, and D.N. Rao, "Fluoride Injury
Symptoms in Epiphytic Lichens and Mosses," Can. J. Bot., 49:1691-1698,
1971.
9. Gilbert, O.L., "The Effect of Airborne Fluoride on Lichens,"
Lichenologist, 5:26-32, 1971. Nash, T.H. III, "Lichen Sensitivity
to Hydrogen Fluoride," Bulletin Torrey Botanical Club, 98:103-106,
1971.
10. Carlsson, C.E., and J.E. Dewey, "Environmental Pollution
by Fluorides in Flathead National Forest and Glacier National Park,"
USDA, U.S. Forest Service, Missoula, Montana, 1971.
11. Dewey, J.E., "Accumulation of Fluorides in Insects Near
an Emission Source in Western Montana," Environ. Entom., 2:179-182,
1973.
12. U.S. Environmental Protection Agency, Environmental Effects
of Fluoride: Glacier National Park and Vicinity, Report No. EPA-908/1-74-001,
Air and Water Programs Division, Region VIII, Denver, Colo., Feb
1974.
13. Kay, E., "An Inquiry into The Distribution of Fluoride
in the Environment of Garrison, Montana," Fluoride, 7(1):7-31m
1974.
14. Macuch, P., E. Hiuchan, J. Mayer, and E. Abel, "Air Pollution
by Fluoride Compounds near an Aluminum Factory," Fluoride Quarterly
Reports, 2(1): 28-32, 1969.
15. Hindawi, I.L. Air Pollution Injury to Vegetation, Nat. Air
Poll. Cont Admin, Pub. No. AP-71, Raleigh, N.C., 1970. Lillie, loc.
cit.
16. Carlson and Dewey, loc. cit
17, Fujii, M., and S. Honda, "The Relative Oral Toxicity of
Some Fluorine Compounds for Silkworm Larvae," J. Sericul. Scl.
Japan,, 41(2):104-110, 1972 (Abstract in EngIlsh).
18. Johansson, T.S.K., and M.P. Johansson, "Sublethal Doses
of Sodium Fluoride Affecting Fecundity of Confused Flour Beetles."
J. Econ. Entom.. 65(2):356-357, 1972.
19. Dobbs, G., "Fluoride and the Environment," Fluoride,
7(3).1123-134, 1974. Marler, J.R., and D. Rose, Environmental Fluoride,
Pub. No. 12,226, National Research Council of Canada, Ottawa, 1971.
20. Riley, J.P., and G. Skirrow, Chemical Oceanography, vol. 2,
Academic Press, New York, 1965.
21. U.S. Environmental Protection Agency, Development Document for
Proposed' Effluent Limitations Guidelines and New Source Performance
Standards for the BASIC FEW TILIZER CHEMICALS Segment of the Fertilizer
Manufacturing Point Source Category, Report No. EPA 440/1-73-011,
Washington, D.C., Nov. 1973; Development Document for Proposed Effluent
Limitations Guidelines and New Source Performance Standards for
the PRIMARY ALUMINUM SMELTING Subcategory of the Aluminum Segment
of the Nonferrous Metals Manufacturing Point Source Category, Report
No. EPA 440/1-73-019a, Dec. 1973.
22. The estimated tonnage of fluoride discharged as water pollution
by the phosphate industry was calculated as follows: Some 40 million
tons of phosphate rock are mined annually in the U.S.. which may
contain 2.5 to 4.5 percent fluoride by weight (USEPA, Rep. No. EPA
440/1-73-011, ibid.). From 30 to 90 percent of the fluoride may
be evolved in gaseous or particulate form in the processing of the
rock into various phosphate products (USEPA, ibid.; Marier and Rose,
loc. cit.). If it is assumed that the average fluoride content of
rock processed is 3 percent and that 50 percent of this is evolved
in processing, some 600,000 tons of potential fluoride air pollutants
will be generated. Air pollution control devices range up to 99
percent, plus. in efficiency; thus up to 594,000 tons of fluoride
(or more) Is likely to be retained in scrubber liquors. Lime treatment
and settling in gypsum ponds can remove 95 to 99 percent of the
fluoride from wastewaters. Lacking exact data on the efficiency
of control measures currently employed throughout the industry,
I have simply assumed that between 1 percent and 5 percent of the
fluoride in waste streams eventually reaches the environment In
effluent discharges, that is 5,940 to 29,700 tons per year. If the
actual state of controls in the industry averages less than 95 percent
efficient, the figure would of course be higher.
23. U.S. EPA, Rep. No. EPA 440/1-73-011, loc. cit.
24. U.S. Public Health Service, Fluoridation Census, National Institutes
of Health, Bethesda, Md., 1970.
25. The estimate for the amount of fluoride added to community water
supplies for dental caries prevention is based on the following
data and assumptions: The average optimal level is assumed to be
1.0 ppm, for simplicity. The average per capita water consumption
from public water supplies Is about 160 gallons per day, all of
which must of course be fluoridated at I ppm, even though per capita
ingestion of water averages only about one quart or so. (Consumption
data from Todd, D.K., The Water Encyclopedia, Water Information
Center. Part Wasington, N.Y., 1970). With approximately 100,000.000
Americans. living in communities which now fluoridate their water,
23,800 metric tons per year of fluoride are put into the water.
Since most water supplies contain some fluoride already (average
0.1 to 0.2 ppm), the figure was rounded off to 20,000 tons.
26. Masuda, T.T., "Persistence of Fluoride from Organic Origins
In Waste Waters," Developments in Industrial Microbiology,
5:53-70, 1964.
27. Marier and Rose, loc. cit.
28. U.S. Geological Survey, Water Quality Data, 1967, Part 11, USGS
Water Supply Paper No. 2015, Dept. of the Int., Washington, D.C.,
1972.
29. US. Geological Survey, Water Quality Data, 1962, Parts 9-14,
USGS Water Supply Paper No. 1945, Dept. of the Interior, Washington,
D.C., 1964.
30. BahiS, L.L., "Diatom Response to Primary Wastewater Effluent,"
J. Water Poll. Cant. Fed. 45:134-144, 1973. Soitero, R.A., "Chemical
and Physical Findings from Pollution Studies on the East Gallatin
River and its Tributaries," Water Research, 3:687-706, 1969.
31. Wang, W.C., and R.L. Evans, "Dynamics of Nutrient Concentration
in the Illinois River,". J. Water Poll. Cant. Fad.. 42: 2 117'3123,
19M.
32. Miller. G.R., Jr., K. Woolsey, and D.R. Kester, "Fluoride
Chlorinity Ratios In Narragansett Bay." Graduate School of
Oceanography, University of R.I, Kingston, R.I., ref. no. 72-1,
1972.
33. Kitime, Y., and V. Furukawa, "Distribution of Fluoride
in Waters of Tokyo Bay," J. Oceanographic Sac. Japan, 28(3):121-125,
1972.
34. Moore, O.J.. "The Uptake and Concentration of Fluoride
by the Blue Crab, Callinectes sapidus," Chesapeake Science,
12:1-13, 1971.
35. McKee, J.E., and H.W. Wolf, Water Quality Criteria, California
State Water Quality Control Board, Pub. No. 3a, Sacramento, Calif.,
1963. Federal Water Pollution Control Administration, Water Quality
Criteria, report of the National Technical Advisory Committee on
Water Quality Criteria, to the Secretary of the Interior, USGPO,
Washington, D.C., 1968. U.S. Environmental Protection Agency, Inorganic
Fertilizer and Phosphate Mining Industries: Water Pollution and
Control, Rep. No. EPA 12020 FPD 09/71, Washington, D.C., Sept. 1971.
36. Sprague, J.B., "Measurement of Pollutant Toxicity to Fish,
III. Sublethal Effects and 'Safe' Concentrations," Water Research.
5-245-266, 1971.
37.Wantland, W.W., "Effects of Various Concentrations of Sodium
Fluoride on Parasitic and Free-living Protozoa and Rotifera,"
J. Dental Res., 35:763-772, 1956. Grune, W.N., and R.Q. Sload, "Effect
of Fluoride Concentration on Sludge Digestion," Sewage &
Industrial Wastes. 27:1-7, 1955. Vajdic, A.H., "The Effect
of Sodium Fluoride on the Growth and Survival of Some Bacterial
Species Important in Water Quality Measurement," Ontario Water
Resources Commis. sion, Division Research Paper No. 21006, 1966.
38. Smith, A.O., and B.R. Woodson, "The Effects of Fluoride
an the Growth of Chlorella pyrenoidosa," Virg. J. Sci., 16:1-8,
1965.
39. McKee and Wolf, loc. cit.
40. Rao, K.V., A.K. Khandekar, and D. Vaidyanadham. "Uptake
of Fluoride by Water Hyacinth, Eichhornia crassipes," Indian
J. Exper. Bio., 11:68-69, 1973.
41. Young, G.E., and W.M. Langille. "The Occurrence of Inorganic
Elements in Marine Algae of the Atlantic Provinces of Canada,"
Can. J. Bot., 36:301-310, 1958.
42. Hemens, J., and R.J. Warwick, "The Effects of Fluoride
on Estuarine Organisms," Water Research. 6:1301-1308, 1972.
43. Danilova, V.V., "The Geochemistry of Dispersed Fluorine.
11. Determination of Fluorine in Plants," Trav. Lab. Biogeochim.
Acad. Sci. URSS, 7:83-85, 1944 (English Abstract. Chemical Abstracts,
1947).
44. Mun, A.I., Z.A. Bazilevich, and K.P. Budeyeva, "Geochemical
Behavior of Fluorine in the Bottom Sediments of Continental Basins,"
Geochem. Internat., 3:698-703, 1966. Windom, H.L., "Fluoride
Concentration in Coastal and Estuarine Waters of Georgia,"
Limnology and Oceanography, 16:806-810, 1971. Kilham, P., and R.E.
Hecky. "Fluoride: Geochemical and Ecological Significance in
East African Waters and Sediments," Limnology and Oceanography,
18(6):932-945, 1973.
45. Sanders, H.O., and O.B. Cope. "Toxicities of Several Pesticides
to Two Species of Cladocerans." Trans. Am. Fish. Soc., 95:165-169,
1966. Anderson, B.G., "The Toxicity Thresholds of Various Sodium
Salts Determined-by the Use of Daphnia Magna " Sewage, Works
J., 18:82-97, 1946. Bringmann, G., and R. Kuhn, "The Toxic
Effects of Waste Water on Aquatic Bacteria, Algae, and Small Crustaceans,"
Gesund-heits-ing., 80-115-123, 1959. FWPCA, loc, cit.
46. Stewart, J.E., and J.W. Cornick, "Lobster (Homarus americanus)
Tolerance for TRIS Buffer. Sodium Fluoride, and Seawater Extracts
of Various Woods," J. Fish. Res. Board Can., 21:1549-1556,
1964.
47. Moore, D.J., "A Field and Laboratory Study of Fluoride
Uptake by Oysters," Report No. 20, Water Resources Research
Institute, University of N.C., Raleigh, N.C.
1969. Moore, 1971, loc. cit. Hemens and Warwick, loc. cit.
48. Moore, 1971, loc. cit. Hemens and Warwick, loc. cit.
49. Neuhold, J.M., and W.F. Sigler, "Effects of Sodium Fluoride
on Carp and Rainbow Trout," Trans. Am. Fish. Soc.. 89:358-370,
1960. Angelovic, J.W., W.F. Sigler. and J.M. Neuhold, "Temperature
and Fluorosis in Rainbow Trout," J. Water Poll. Cont. Fed.,
33:371-381. 1961. Neuhold, J.M. and W.F. Sigler, "Chlorides
Affect the Toxicity of Fluorides in Rainbow Trout," Science,
135:732-733, 1962. Herbert. D.W.M., and D.S. Shurben, "The
Toxicity of Fluoride to Rainbow Trout," Water & Waste Treatment.
10:141-142, 1964. Vallin, S., "The Toxicity of Fluoride to
Fish," Vatten, 24:51-57, 1968. Sigler, W.F., and J.M. Neuhold,
"Fluoride Intoxication in Fish: A Review," J. Wildlife
Diseases, 8:252-254, 1972. DeRoos, C.D., "The Effects of Sodium
Fluoride on the Weight Gain and Gills of the Common Goldfish,"
Thesis, Utah State University, Logan, Utah, 1957. Ellis. M.M., B.A.
Westfall, and M.D. Ellis, "Determination of Water Quality,"
Research Report No. 9. U.S. Fish and Wildlife Service, U.S. Dept.
of the Int., Washington. D.C., 1948. Wallen, I.E., N.C. Greer. and
R. Lasater, "Toxicity to Gambusia affinis of Certain Pure Chemicals
in Turbid Waters." Sewage and Industrial Wastes, 29:695-711,
1957. Simonin, P., and A. Plerron, "Toxicite Brute des Derivis
Fluores," Comptes Rendus, 124:133-136, 1937. Hemens and Warwick,
loc. cit.
50. Sigler and Neuhold, ibid.
51. Ellis et al., loc. cit.
52. Fisher, F., and M.J. Prival, Total Fluoride Intake, Center for
Science in the Public Interest, Washington, D.C., 1973. Neuhold
and Sigler, loc. cit. Ke, P.J., H.E. Power, and L.W. Regier, "Fluoride
Content of Fish Protein Concentrate and Raw Fish," J. Sci.
Food Agric., 2 1 : 108-109. 1970.
53. Simonin and Pierron, loc. cit.
54. Kaplan, H.M., N. Yee, and S. Glaczenski. "Toxicity of Fluorides
for Frogs," Laboratory Animal Care, 14:185-189, 1964.
55. Cameron, J.A., "The Effect of Fluoride on the Hatching
Time and Hatching Stage in Rana pipiens." Ecology, 21:288-292,
1940. Kuusisto, A.N., and A. Telkka, "The Effect of Sodium
Fluoride on the Metamorphosis of Tadpoles," Acta Odontologica
Scandanavica, 19:121-127, 1961. Kawahara, H., and K. Kawahara, "Pretiminay
Report on the Influence of NaF Solution Upon the Early Development
of Toad Embryos." Tokushima J. Exper. Mod.. 1:98-104, 1954.
(Extended abstract appeared in Fluoride, 4(4):167-171, Oct. 1971.)
56. Kuusisto and Telkka, ibid.
57. Hiuchan, E., J. Mayer, and E. Abel, "The Influence of Aluminum
Works Exhalations on the Content of Fluorides in Soil and Grass,"
Pol'nohospodarstvo, 10(4): 257-262, 1964. (in Slovak. English Abstract
in U.S. Environmental Protection Agency, Air Pollution Aspects of
Emission Sources: PRIMARY ALUMINUM PRODUCTION - A Bibliography With
Abstracts, Pub. No. AP-119, Air Pollution Technical Information
Center, Research Triangle Park, N.C., June 1973.)
58. Oelschlager. W., "Fluoride Uptake in Soil and its Depletion,"
Fluoride, 4(2):80-84, 1971.
59. Chemical and Engineering News, June 3, 1974.
60. Garber, PC. "Fluoride Uptake in Plants," Fluoride
Quarterly Reports, 1(1):27-33, 1968.
61. Gisiger, L., "The Solubility of Various Fluorine Compounds
in Soil," Fluoride Quarterly Reports, 1(1):21-26, 1968. Macuch
et al., loc. cit.
62. Macintire, W.H., "Air Versus Soil as Channels for Fluoric
Contamination of Vegetation in Two Tennessee Locates," In McCabe,
L.C., ed., Proceedings, U.S. Technical Conference. on Air Pollution,
Interdepartmental Committee on Air Pollution, Washington, D.C.,
1950, pp. 53-58.
63. Gisiger. loc. cit.
64. Jurkowska, H., "Toxicity of Fluorine to Crop Plants as
Depending on the Form of Nitrogen Fertilizer," Acta Agrar..
Silvestria Ser. Agrar., 11:19-37, 1971. (in Polish. English summary.)
65. Bovay, E. "Fluoride Accumulation in Leaves due to Boron-Containing
Fertilizers," Fluoride Quarterly Reports, 2(4):222-223, 1969.
Bolay, A., E. Bovay, J.P. Quinche, and R. Zuber, "Amounts of
Fluorine and Boron in the Leaves and Fruits of Fruit trees and Vinyards,
Fertilized by Certain Boron- and Fluorine-Containing Fertilizers,"
Revue Suisse de Viticulture et Arboricultural, (Laussane), 3(3):54-61,
1971.
66. Gardner, loc. cit. Bovay, ibid.
67. Hadjuk, J., "Extension Growth in Seedlings as a Biological
Test of Soils Contaminated with Fluorine Exhalates," Biologia,
24(10):728-737, 1969. (In German; English abstract in U.S. EPA Pub
No. AP-119, loc. cit.)
68. Davis, J.B., and R.L. Barnes, "Effects of Soil-Applied
Fluoride and Lead on Growth of Loblolly Pine and Red Maple,"
Environmental Pollution, 5(1):34-44, 1973.
69. Smith, R.L., Ecology and Field Biology, Harper and Row, N.Y.,
1966.
70. Hall, R.J., "The Analytical Partition of the Fluorine
Compounds in Some Tropical Plants and Soils," Fluoride Quarterly
Reports, 1(1):9-14, 1968.
71. Hall, R.J., "The Distribution of Organic Fluoride in Some
Toxic Tropical Plants," New Physiology, 71:855-871, 1972.
72. Vickery, B., and M.L. Vickery, "Fluorine Metabolism in
Dichapetalum toxicarium," Phytochemistry, 11:1905-1909, 1972.
73. Miller, G.W., M.H. Yu, and M. Psenak, "Presence of Fluoro-organic
Compounds in Higher Plants," Fluoride, 6(4):203-215, 1973.
74. Wade, R.H., J.M. Ross, and H.M. Benedict, "A Method for
the Detection and Isolation of Traces of Organic Fluorine Compounds
in Plants," J. Chromatography, 14:37-45, 1964.
75. Lovelace, C.J., G.W. Miller, and G.W. Welkie, "The Accumulation
of Fluoroacetate and Fluorocitrate in Forage Crops Collected Near
a Phosphate Plant," Atmospheric Environment, 2:187-190, 1968.
76. Cheng, J.Y., M.H. Yu, G.W. Miller, and G.W. Welkie, "Fluoro-organic
Acids in Soybean Leaves Exposed to Fluoride," Environ. Sci.
and Tech., 2:367-370, 1968.
77. Peters, R.A., and M. Shorthouse, "Formation of Monofluorocarbon
Compounds by Single Cell Cultures of Glycine max Growing on Inorganic
Fluoride," Phytochemistry, 11:1139, 1972.
78. Ward, P.V.V., and N.S. Huskisson, "The Metabolism of Fluoroacetate
by Plants," Biochem. J., 113:9-18, 1969.
79. Weinstein, L.H., D.C. McCurie, F. Mancini, L.J. Colavito, D.H.
Silberman, and P. van Leuken, "Studies on Fluoro-organic Compounds
in Plants, III. Comparison of the Biosynthesis of Fluoro-organic
Acids to Acacia georginae with Other Species," Environ. Res.,
5:393-408, 1972.
80. Peters, R.A., and M. Shorthouse, "Fluorocitrate in Plants
and Foodstuffs," Phytochemistry, 11:1337-1338, 1972.
81. Peters, R.A., "Organic Fluorides in Plants," Fluoride,
6(3):189-194, 1973.
82. Peters, J.A., and K.J. Baxter, "Analytical Determination
of Compound 1080 (Sodium Fluoroacetate) Residues in Biological Materials,"
Bull of Environ. Contamination and Toxic., 11(2):177-183, 1974.
83. Hall, R.J. and R.B. Cain, "Organic Fluorine in Tropical
Soils," New Phytology, 71:831-853, 1972.
84. Preuss, P.W., A.G. Lemmens, and L.H. Weinstein, "Studies
on Fluoro-organic Compounds in Plants, I. Metabolism of 2-14 C-Fluoroacetate,"
Contrib. Boyce Thompson Institute, 24:25-31, 1968. Preuss, P.W.,
and L.H. Weinstein, "Studies on Fluoro-organic Compounds in
Plants, II. Defluorination of Fluoroacetate," Contrib. Boyce
Thompson Institute, 24:151-155, 1969.
85. Sargent, D.F., and C.P.S. Taylor, "The Effect of Cupric
and Fluorie Ions on the Respiration of Chlorella," Canadian
J. Botany 50:905-907, 1972.
86. Marier, J.R., "The Ecological Aspect of Fluoride,"
Fluoride 5(2):92-97, 1972.
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