£2^- 3^2-
Environmental Pollution by Fluorides
in FLATHEAD NATIONAL FOREST and GLACIER NATIONAL PARK
By
Clinton E. Carlson, Plant Pathologist
and
Jerald E. Dewey, Entomologist
^55. 1.6AAVS.
mow***
U«tA*T
U. S. DEPARTMENT OF AGRICULTURE
FOREST SERVICE
Division of State and Private Forestry
Forest Insect and Disease Branch
Missoula, Montana
Cover Photographs
Top — Plume created by the Anaconda Aluminum Company Plant at Colum-
bia Falls, Montana. Teakettle Mountain is in background.
Bottom — Fluoride injury on lodgepole pine caused by emissions from the
Anaconda Aluminum Company Plant.
October, 1971
AFPS / OGDEN, UTAH / 72-203
/\//C-P5 # s~a/
PROPER'
DEPARTMENT CP
STATE OF
LAN
u:
A A
ik
Environmental Pollution
by Fluorides
in FLATHEAD NATIONAL FOREST
and GLACIER NATIONAL PARK
By
Clinton E. Carlson, Plant Pathologist
and
Jerald E. Dewey, Entomologist
U. S. DEPARTMENT OF AGRICULTURE - FOREST SERVICE
Northern Region Headquarters
Division of State and Private Forestry
Forest Insect and Disease Branch
Missoula, Montana
Digitized by the Internet Archive
in 2016
https://archive.org/details/environmentalpol1971carl
Table of
Contents
Page
Summary i
Introduction 1
Literature Review 2
Origin of fluorides 2
Effects on vegetation 2
Accumulation and symptoms on plants 3
Entomological effects 3
Environmental effects 3
Methods, Pathological Phase 4
Description of the area 4
The aluminum plant 4
Field study design 4
Laboratory study design 6
Histological analyses 6
Aerial photography 8
Methods, Entolomological Phase 8
Accumulation of fluoride by insects 8
Insect population sampling 8
Results, Pathological Phase 10
Parameters 10
Control plots 10
Radial system 10
Page
Special samples 18
Relation between injury index and fluoride content 20
Rates of accumulation 20
Histological results 20
Aerial photography 23
Results, Entomological Phase 26
Fluoride accumulation by insects 26
Insect population sampling 26
Discussion and Conclusions 28
General 28
Rates of accumulation : 28
Susceptibility of species 28
Ecological Implications 29
Pollution in Glacier National Park 29
Pollution in Coram Experimental Forest 29
Insects and fluoride 29
Economic and esthetic damage 30
Future plans 30
Acknowledgements 31
Literature cited 32
Appendixes 34
LIST OF FIGURES
1. Fluoride study area 5
2. Anaconda Aluminum Reduction Plant 7
3. Location of special sample areas 9
4. Schematic of fluoride gradients 13
5. Profile of radius 4 14
6. Profile of radius 5 15
7. Profile of radius 6 16
Page
8. Isopols of fluoride pollution ' .... 17
9. Insect and fluoride injury 19
10. Fluoride burn on lodgepole pine 21
11. Fluoride burn on lodgepole pine 21
12. Terminal dieback of Douglas-fir 22
13. Hypertrophied phloem and transfusion parenchyma 23
14. Hypertrophied nuclei of mesophyll cells 24
15. Hypertrophied epithelial cells 25
16. Regression of scale counts on fluoride 27
LIST OF TABLES
I-A Analysis of variance of control data 11
I- B Means for factors, control data 11
II Classification of visual injury 18
III Rates of fluoride accumulation 20
LIST OF APPENDIXES
I Common and scientific names of plants and animals 34
II- A Tabulation of radial and control data, first sampling 37
II- B Tabulation of radial and control data, second sampling 40
III- A Area polluted by fluorides, all lands studied 43
III-B Area polluted by fluorides, Glacier National Park 44
IV Fluoride content and injury index values for special samples 45
V Regression analysis of injury index on fluoride content 50
VI Fluoride accumulation levels in insects 51
VII Larch casebearer per 100 spurs sampled 53
VIII Pine needle scales per 600 lodgepole needles 54
IX Pine needle scales per 600 ponderosa needles 55
X Regression analysis of pine needle scales on fluoride content 56
Summary
The U. S. Forest Service initiated a study in
1969 to determine: (1) the major cause of vege-
tational injury and damage on forested lands
proximal to the Anaconda Aluminum Com-
pany, (2) the source of the cause, (3) the area
affected, (4) whether insects were accumu-
lating fluorides, and (5) if insect populations
were being affected by fluorides.
Fluorides emitted from the Anaconda
Aluminum Company were determined to be
the primary cause of the injury and damage to
vegetation in the surrounding area. Isopols,
lines of equal pollution, were established for
the area. Highest fluoride concentrations, up to
1000 ppm1 , in foliar tissue were found near the
Anaconda aluminum plant. Data indicated the
fluorides were carried by air movement from
the aluminum plant through a saddle in Tea-
kettle Mountain to Glacier National Park, fol-
lowing the pattern of the prevailing winds in
the area. Elevated fluorides (greater than 10
ppm) were found in vegetation on Columbia
Mountain and Teakettle Mountain, in vegeta-
tion near the towns of Columbia Falls, Hungry
' ppm — parts per million
Horse, and Coram, Montana, and in the south-
west portion of Glacier National Park. Varying
degrees of visible fluoride injury were found on
vegetation over more than 69,120 acres. Ele-
vated fluorides were found in vegetation on
nearly 214,000 acres of forested lands of mixed
ownerships.
Although fluoride emissions were reduced
during the summer of 1970, fir and spruce trees
continued to accumulate fluorides at the same
rate as in 1969.
Definite histological reactions to elevated
fluorides occur in conifer needle tissue, in-
cluding hypertrophy of parenchymatous cells.
Fluorides also were found to accumulate in
insect tissue. All groups of insects studied con-
tained high fluoride levels. Pollinators pos-
sessed the highest, up to 406 ppm. Cambium
feeders contained in excess of 52 ppm, indi-
cating that fluoride must be translocated in the
cambium of trees. Predatory insects had fluo-
ride counts over 53 ppm, showing fluoride is
passed along the food chain. Insect population
samples indicated that elevated fluoride levels
in pine needles leads to a buildup of the pine
needle scale.
Introduction
On August 15, 1955, the Anaconda Com-
pany formally dedicated a new aluminum re-
duction plant on their lands at Columbia Falls,
Montana adjacent to the Glacier View Ranger
District, Flathead National Forest. Partial oper-
ation of the plant had already begun using the
Vertical Soderberg anode pot system. Ana-
conda Company officials insisted that injury
caused to vegetation and animals by emitted
fluorides would be negligible. F. J. Nietzling,
Supervisor of the Flathead National Forest,
wrote a letter to Glacier View District Ranger
Mel Yuhas on June 27, 1957, and indicated
ponderosa pine1 trees in the vicinity of the re-
duction plant were dying. Subsequently, in
July of 1957, Ranger Mel Yuhas, Bert Morris,
Forester on the Glacier View District, and Don
Leaphart2 , pathologist, Forest Service Inland
Empire Research Center, inspected suspected
fume damage near the aluminum plant. In a
Forest Service memorandum Leaphart ex-
pressed his opinion that the injury was caused
by fluoride fumes escaping from the reduction
works. Little in the way of evaluation was done
subsequently until 1969. In the meantime, the
Anaconda Company expanded the plant in
1 Scientific names of all plant and animal species
mentioned in this report are listed in Appendix I.
2 Now at Intermountain Research Station,
Moscow, Idaho.
1964-1965 and again in 1967-1968. Following
the 1968 expansion and increased production,
dead and dying trees and foliage necrosis were
observed over the entire west face of Teakettle
Mountain immediately east of the reduction
works.
In preliminary evaluations in June and
November 1969, we found tissue necrosis and
elevated fluoride levels in 26 of 35 vegetation
samples consisting of ponderosa pine, lodge-
pole pine, western white pine, and Douglas-fir.
It became obvious that a detailed evaluation
was needed to accurately assess the problem. In
January of 1970 a study plan, designed to
analyze the fluoride problem, was finalized.
Our hypothesis was that fluorides from the
aluminum plant were causing ecological dam-
age to flora and fauna. To test this hypothesis,
the following objectives were outlined:
1. Identify the major cause of vegetational
injury and damage on forested lands near the
aluminum plant.
2. Identify the source of the cause.
3. Determine the area affected.
4. Determine if insects accumulate
fluorides.
5. Determine if insect populations were
fluctuating relative to the injury.
This report is divided into two phases: Path-
ological, dealing with objectives 1-3, and
entomological, dealing with objectives 4 and 5.
1
Literature
Review
Origin of Fluorides
Electrolytic reduction of alumina (AI2O3)
produces pure aluminum. The electrolysis is
done within a reduction cell or “pot” and is
accomplished in the presence of the electrolyte
cryolite (3 NaF-AlF3). Sodium fluoride (NaF)
and aluminum fluoride (AIF3) are released in
particulate form as waste during the high tem-
perature electrolysis (965° to 975° C.), and
hydrogen fluoride (HF) and small quantities of
carbon tetrafluoride (CF4) are released as gases
(Hickey, 1968). Hydrocarbons in considerable
amounts are released. NaF, AIF3, and HF are
accumulated by and cause injury to plants. Al-
though no highly reliable figures are available,
it has been estimated that about half of the
emissions are gaseous and half particulate
(Semrau, 1957).
Fluoride emissions can be contolled to vari-
ous extents by a process known as scrubbing.
This involves the injection of a high-pressure
spray of water or lime solution into the effluent
stacks or the application of a low pressure
scrubbing system, resulting in absorption of the
fluorides (Hickey, 1968).
Effects on Vegetation
General. During the past 20 years, effects of
fluorides on vegetation have been studied quite
extensively in laboratory-controlled experi-
ments and in field experiments proximal to
aluminum reduction plants. Shaw, et. al.
(1951) reported foliar necrosis and retarded
diameter growth in ponderosa pine near the
Kaiser Aluminum Company aluminum reduc-
tion plant at Mead, Washington. The injury
could not be attributed to insects, fungi, nor
climate, but was highly correlated with exces-
sive foliar fluoride concentrations ranging to
600 ppm dry weight basis. Lynch (1951) found
nearly a sixfold decrease in diameter growth
rate in ponderosa pine near the same reduction
plant and attributed the effect to fluorides.
Adams, et. al. (1956) tested the sensitivity of
2
ponderosa pine as an indicator of fluoride pol-
lution and found it readily express visual
symptoms (foliar necrosis).
A study made near the Harvey Aluminum
Company reduction plant at The Dalles,
Oregon (Compton, et. al. 1961), showed foliar
necrosis of ponderosa pine to be related to ele-
vated fluoride levels and not to fungal, climatic,
nor insect agents. They also found abnormally
large concentrations of black pine leaf scale
in the affected area.
Treshow, et. al. (1967), reported mortality
and growth decline of Douglas-fir near a phos-
phate reduction plant in Idaho. They found up
to 100 percent reduced diameter growth when
the foliar fluoride concentrations exceeded 50
ppm. Interestingly, they found increased shoot
and needle elongation under insidious levels of
fluoride pollution, but concluded the increased
length was due to abnormal cell elongation and
not excessive division.
Accumulation and Symptoms on Plants
Fluorides enter needles and leaves mainly
through stomata. Once in the foliar tissue, they
are in a soluble state, free-flowing and tend to
accumulate at conifer needle tips or broadleaf
margins, causing tip or margin necrosis. Be-
cause particulate fluorides are readily adsorbed
to dust particles, dust on the leaf surface may
aid in accumulating fluorides (Jacobson, et. al.
1966).
Hindawi (1970), through the use of colored
pictures, vividly portrayed symptoms of fluo-
ride injury. Browning of leaf margins and
needle tips associated with a distinct demarca-
tion line between healthy and injured tissue
was a constant indicator of fluoride pollution.
Reductions in photosynthesis have been
shown to occur in fluoride fumigated plants.
Thomas (1961) reported a decrease in photo-
synthesis of up to 45 percent on Gladiolus
plants, resulting in decreased plant vigor and
growth.
Entomological Aspects
The literature pertaining to the effects of
fluorides on insect populations is limited. In a
study of blighted ponderosa pines near an
aluminum reduction facility, Johnson (1950)
found a significant increase of the black pine
leaf scale as tree damage caused by fluorides
increased. Lezovic (1969) indicated that in a
study conducted near an aluminum factory “all
colonies of bees, a total of 70, died off.” Other
authors reporting on fluoride injury to bees in-
clude Caparrini (1957), Guilhon et. al. (1962),
Marier (1968), and Maurizio and Staub (1956).
Outram (1970) concluded sulphuryl fluo-
ride caused a reduction in oxygen uptake and
changes of respiratory quotient in the eggs of
the desert locust, and the yellow meal worm.
He said, “it is suggested that sulphuryl fluoride
is nonspecific in respect to sites of attack in the
insect egg and inhibits several metabolic
processes.”
Pollution by chemicals other than fluorides
has been reported to indirectly affect insect
populations. Stark et. al. ( 1968) in a study deal-
ing with oxidants of photochemical air pollu-
tion (particularly ozone) stated that “air pollu-
tion injury predisposed ponderosa pine to bark
beetle infestations.”
Environmental Effects
Maclean et. al. ( 1969) showed that livestock
forage accumulated enough fluorides to be a
potential hazard to livestock. Little fluoride is
taken in by breathing; most is ingested through
foods, forage, etc. Marier et. al. (1969) pointed
out that excessive inorganic fluorides in ani-
mals tend to be either excreted through the
kidneys or accumulated in the teeth and skele-
tal tissues. In acute cases, excessive fluorides
have caused skeletal fracture and disintegration
of teeth, associated with severe pain. Normally,
in animals feeding on foliage not contaminated
by fluorides, fluorides in bones do not exceed
1000 ppm. However, ingestion by animals of
fluoride-contaminated forage can lead to fluo-
ride accumulations of 5000 ppm or more, at
which levels severe fluorosis can occur (Marier,
1969).
Gordon ( 1969) in a study near the Cominco
American phosphate fertilizer plant in western
Montana found large concentrations of fluo-
rides in femur bones of Columbian ground
squirrel and concluded the fluorides were in-
gested with the contaminated forage. Available
forage in the area was found to have excessive
fluorides. No fluorosis in the animals was
indicated.
3
Methods
Pathological Phase
Description of the Area
The Anaconda Aluminum Company reduc-
tion plant is located about 2 miles east of
Columbia Falls, Montana, (fig. 1) at 3,100 feet
m.s.l. (mean sea level). Teakettle Mountain
rises abruptly to 5,936 feet m.s.l. immediately
east of the plant. Columbia Mountain is 2 miles
south and Glacier National Park 6 miles north-
east of the plant. Topography west and south-
west of the reduction plant is quite flat for 10
to 1 5 miles, but mountainous with deep valleys
to the northwest, north, northeast, and south-
east. The higher peaks in the general area attain
an elevation of 8,000 to 9,000 feet m.s.l. The
prevailing wind is southwesterly.
Because of the variable topography, a num-
ber of different habitat types are represented.
The more common are: Pseudotsuga
menziesii — Symphoricarpos albus h.t., Abies
lasiocarpa — Xerophyllum tenax h.t.; and
Pinus albicaulis — Abies lasiocarpa h.t.
(Daubenmire and Daubenmire, 1968). A large
variety of fauna, from grizzly bear and elk to
small rodents, proliferate in the area.
The Aluminum Plant
The reduction plant is owned by the Ana-
conda Company. The physical plant is com-
posed of five pot lines, each line containing 120
individual reduction pots, for a total of 600
pots(fig. 2). The Vertical Stud Soderberg Pot
system is used for reducing the alumina to pure
aluminum, a process shown to be one of the
most problematical in terms of controlling
effluents.
During 1969 and early 1970 the Anaconda
Company reported fluorides were emitted at a
rate of nearly 7,600 pounds per day but were
reduced to about 5,000 pounds by September
of 1970. By early May, 1971, company of-
ficials reported emissions were reduced to
2,500 pounds per day. Although the fluoride
component of the effluent plume is nearly in-
visible, the hydrocarbon portion readily indi-
cates the general direction of atmospheric F
transport of the pollutants.
Field Study Design
Control Plots. Two areas, one 30 miles south
of Columbia Falls near Big Fork, Montana, and
the other 30 miles west of Columbia Falls,
about 15 miles west of Kalispell, Montana,
were selected for control sampling. The loca-
tions were upwind of the aluminum plant in
terms of the general prevailing southwesterly
winds. Three plots, each one-hundredth acre in
size (6.6 feet wide by 66 feet long), were in-
stalled in each area. All conifers and shrubs on
the plots were sampled. Also, representative
herbaceous plants and at least one grass species
were sampled. We collected control samples in
June-July and again in September-October,
1970.
Radial System. Ten radii, numbered con-
secutively from 1 to 10, were established ex-
tending from the aluminum plant into adjacent
forested lands (figure 1). The direction of each
radius was based on two criteria: (1) it must
transect National Forest land, and (2) it should
follow suspected wind channels. On each
radius, basic plots one-hundredth acre in size
(6.6 feet wide by 66 feet long, oriented longi-
tudinally) were established at one-fourth, one-
half, 1, 2, 4, 6, and 8 miles from the plant. Be-
4
5
cause radii 4, 5, and 6 intercepted Glacier Na-
tional Park, additional plots were established at
10, 12, and 14 miles on radii 4 and 5 and at 14
miles on radius 6 to sample vegetation in the
Park. Each plot was permanently established as
witnessed by driving a wooden stake at the plot
location with plot information written on it.
Collection of Vegetation on Control and
Radial Plots. Plots were sampled twice, once
during June-July 1970, and again in October-
November 1970. For convenience, we termed
the June-July collection the “first sampling”
and the October-November collection the
“second sampling.” About 3 pounds of foliage
on each plot were collected and maintained
separately from one to several representatives
of each conifer species, one representative of
each of two shrub species, and one repre-
sentative of each of one herbaceous and one
grass species. Foliage collected from each grass,
broadleaf plant, and deciduous conifer was
considered a separate sample. Foliage collected
from other conifers was separated by year of
origin, and foliage of each year was considered
a separate sample. Generally only 1969 and
1970 needles were sampled. For conifers, the
sample was always collected from dominant
and codominant trees and always in the upper
one-third of the crown facing the aluminum
plant. Samples from other types of vegetation
were collected as foliage was available.
Special sampling. In addition to the sys-
tematic field design, a supplemental series of
“special samples” were collected in areas
deemed most likely to sustain high fluoride
levels. Because fluorides are transported in at-
mosphere, vegetation on ridges and prominent
topography downwind from the prevailing
winds over the aluminum plant may be more
likely to intercept fluorides than vegetation in
valleys or other areas. The general locations of
special sampling are shown in figure 3. The lo-
cations were: 1) near Columbia Falls, 2)
Columbia Mountain, 3) Teakettle Mountain,
4) Southwest Glacier National Park, 5) Coram
Experimental Forest, near Desert Mountain,
and 6) northeast edge of Hungry Horse Reser-
voir. Samples were not collected on a plot
basis as described for the radial collections;
rather, vegetation representative of the area,
with emphasis on coniferous species, was col-
lected in June and again in October 1970. A
sample was defined as stated in the section on
Collection of Vegetation.
Laboratory Study Design
Visual Burn. All vegetation samples were
brought to the laboratory for analysis of visu-
al burn. For each conifer sample, needles were
sorted according to year of origin, 1969 or
1970. The proportion of different needles
showing evidence of foliar burn was recorded
(Carlson and Dewey, 1970). Also the average
proportion of length of burn on affected
needles was estimated. For shrubs, the pro-
portion of different leaves showing bum
symptoms was estimated, and burned on leaves,
the actual proportion of area affected was es-
timated. Symptoms on grasses could not be
measured. Extreme care was exercised to
avoid confusing insect or disease injury with
fluoride burn.
Chemical Analysis. After estimation of
foliar burn, separate subsamples of 30 to 40
grams of foliar tissue from samples of 1969
and 1970 needles of each conifer species and
from one sample of each of two shmb species
from each plot were prepared for chemical
analysis of available fluorine (i.e., gaseous and
particulate). A subsample of grass and herba-
ceous tissue from each plot was similarly pre-
pared. All samples were sent to WARF Insti-
tute, Inc., Madison, Wisconsin, for analysis.
The semi-sutomated method as outlined by
Health Laboratory Science (1969) was used
for determination of total fluorine. Results
were given in ppm (parts per million) dry
weight basis. For the purposes of this report,
the terms “fluorine” and “fluoride” will be
used interchangeably.
Histological Analyses
Solberg and Adams (1956) and Gordon
(1970) in controlled studies described histo-
logical responses of conifers to fumigations by
fluorides. Protoplasmic and nuclear hyper-
trophy of parenchyma cells resulting in death
of foliar phloem tissue were regarded as
symptomatic of fluorosis in conifer tissue.
Therefore, we arbitrarily selected subsamples
from burned conifer needles for histological
analysis of tissue showing fluoride bum. Ap-
proximately 2 mm. sections of tissue were ex-
tracted from the “transition zone” (that por-
tion between the green and burned tissue on
6
Figure 2. — Anaconda Aluminum Reduction plant at Columbia Falls , Montana. Note effluent
from the five pot lines. View is southerly, Columbia Mountain is in background.
7
the needles). The sections included green,
chlorotic, and necrotic tissue. The specimens
were killed and fixed in formalin-
aceto-alcohol, dehydrated through a tertiary
butyl alcohol series, embedded in paraplast,
sectioned at 9 micra thickness on a rotary
microtome, and examined and photographed
through a Leitz Ortholux phase contrast
microscope equipped with an Aristophot
photographic system.
Aerial Photography
The entire area suspected to be affected by
fluorides was photographed in July of 1970
with Aero Ektachrome, 9x9 format, at a scale
of 1:12000. In addition, stereo pairs were
taken of all the radial plots at a scale of
1:4000.
Entomological Phase
Accumulation of Fluoride by Insects
A broad spectrum of insects including fo-
liage feeders, cambium feeders, pollinators,
and predators were sampled and analyzed for
fluoride accumulation (Appendix VI). At
least 5 grams of each species were oven dried
and sent to WARF for analysis of available
fluoride (5 grams = from 100-500 individual
insects, depending on the species.) Insects
were collected in the spring (June 1), summer
(August 12), and fall (October 9), 1970, on
the basis of their availability. All collections
were made within one-half mile of the alumi-
num plant except for eight control samples
that were taken at least 50 miles from the
plant. The less common insects were sent to
the U. S. National Museum for identification;
the remainder were identified by Jerald E.
Dewey.
Insect Population Sampling
Controls. Two forest insects, larch case-
bearer and pine needle scale, were sampled in
an attempt to relate population numbers to
fluoride accumulations. Control samples were
taken 30 miles to the north, south, east, and
west of the plant. Larch casebearer popula-
tions were measured using the system de-
scribed by Bousfield (1969) in which case-
bearers per 100 larch spurs were measured.
Pine needle scale populations were measured
modifying the method reported by Fischer
(1950) in which scales per linear inch of
“new” and “old” foliage were counted. Val-
ues of scales per 600 needles were obtained.
Radial Sampling. To determine if insect
populations were increasing, decreasing, or re-
maining static in relation to distance from the
suspected fluoride source and to foliar fluo-
ride content, sampling was conducted in mid-
April 1970, for populations of larch case-
bearer and pine needle scale, along the estab-
lished radii. The same procedures were used as
described above. Sample intervals were one-
fourth, one-half, 1, 2, 4, and 8 miles from the
aluminum plant.
8
FIGURE 3
Location of areas in which
special sampling was done.
SCAU
2 3
Mile
N
Teakettle Mtn.«
A
GLACIER
NATIONAL
PARK
% m'
4
Park
i Hdqrs
West
lacier
Lake Five
aacQ
Falls
nHungry
Horse
umbia
'Mtn.
O
FLATHEAD rL
NATIONAL ^
FOREST
6
V
9
Results
Pathological Phase
Parameters
The following parameters were used in the
evaluation of the pollution problem:
1 . Fluoride content — Available fluoride
content of whole leaves and whole needles of
plants, dry weight basis, in ppm.
2. Injury index — The concept of injury
index (I. I.) was developed after the field data
were collected. Let P equal proportion of dif-
ferent needles showing fluoride burn symp-
toms for a given sample and let R equal the
Ratio of length of burn on burned needles of
the same sample, as described previously.
Then the product PR would be an estimate of
the gross amount burned for foliage of a given
year. A similar value can be computed for
broadleaf plants. We have termed this value
the “injury index” for a given sample. Estima-
tions of foliar burn for determining injury in-
dex were done on all samples (except grasses)
collected the first sampling period, but only
on conifers the second. An early freeze caused
premature death of broadleaf foliage, making
estimation of burn nearly impossible.
Control Plots
Fluorine Content. One hundred and nine
control samples, including collections of both
sampling periods, were analyzed chemically.
Data for fluoride accumulation in vegetation
were classified and grouped as shrub, 1969
conifer, 1970 conifer, herbaceous, and grass
(Appendixes II-A and II-B) and were sub-
jected to a four-factor analysis of variance
shown in table I-A. The means for factors are
shown in table I-B.
Only means in vegetation type showed sig-
nificance: the other factors were insignificant.
The significance in vegetation type was vested
between 1970 conifer tissue at 6.17 ppm and
the grass tissue at 10.73. All factors, with the
exception of grass species, had average fluo-
ride content of less than 10 ppm. Therefore,
we selected 10 ppm fluoride as a conservative
control or “background” level for all plant tis-
sue sampled in the study.
Injury Index. For all control samples in the
first sampling the average injury index (I. I.)
was 0.001; for the second sampling was 0.000.
Thus we arbitrarily established a higher
value of 0.006 as a conservative control level
for injury index; i.e., only samples having an
1. 1. greater than 0.006 would be considered
visually injured by fluorides. To further sub-
stantiate 1. 1. as a parameter for evaluating
foliar fluorosis we made a nonparametric anal-
ysis over all the samples, control and other-
wise, including both sampling periods and
found that of 237 samples having an 1. 1. ex-
ceeding 0.006, 227 had fluorine concentra-
tions greater than 10 ppm and 10 had less
than 10 ppm. Thus, 96 percent of the time an
1. 1. exceeding 0.006 was highly indicative
of elevated (abnormal) fluoride levels. How-
ever, many samples having high fluoride
levels did not show injury. Therefore, 1. 1., at
best, is a useful but very conservative param-
eter for estimating fluoride pollution.
Radial System
Fluoride Content. For the purpose of dem-
onstrating general pollution levels, fluoride
10
Table I-A. — Analysis of variance of control data, fluoride content
Source of
variation
Degrees of
freedom
Sum squares
Mean squares
F ratio
Significance
Collection period
1
27.2431
27.2431
2.75
NS1
Area
1
27.4862
27.4862
2.78
NS
Plots
2
23.0648
11.5324
1.17
NS
Vegetation type
4
158.2020
39.5504
4.00
*2
Residual
51
504.3950
9.8900
Total
59
704.3950
1 NS = Nonsignificant
2 * = Significant at the 95 percent level
Table I-B. — Means for factors, control data
Factor
Level
Mean
Collection period
June
7.6713
October
9.018
Area
I
7.668
II
9.021
Plot
1
9.136
2
7.622
3
8.276
Vegetation type
Shrub
8.324
Conifer, 1969
7.076
Conifer, 1970
6.171
Herbaceous
9.423
Grass
10.729
Grand mean
8.344
3 Fluoride content, ppm
11
content values were averaged separately on a
plot-by-plot basis, irrespective of the general
vegetation type. This procedure was consid-
ered quite valid because very nearly the same
amount and type of vegetation was collected
from all plots sampled and would be readily
comparable to the plot-by-plot analysis of
control data mentioned previously. (Control
plot averages did not show significance and
were less than 10 ppm). However, on all 11 of
the plots located very close to the reduction
plant, conifers had been killed, apparently
from fluorides, and samples could not be ob-
tained. Results are tabulated in Appendix II- A
(first sampling) and Appendix II-B (second
sampling). Blanks in data indicate the vegeta-
tion type was not found on the plot. A total
of 1,254 samples obtained during both sam-
pling periods were chemically analyzed.
For every radius there exists a general
trend of very high fluoride content near the
aluminum plant, decreasing to control levels
at the furthest plots. One can easily see from
the tables the same general trend exists for
separate vegetational types as exists for the
plot averages, thus supporting our decision to
use plot averages. In figure 4, the fluoride gra-
dients from the grand average column, Appen-
dix II-B, are schematically portrayed. On all
the radii the lines of increasing concentration
converge at the aluminum reduction plant, in-
dicating the source of the fluorides. In figures
5, 6, and 7, we have graphed for radii 4, 5,
and 6 respectively, the fluoride concentration
data from the grand average column, Appen-
dix II-B (second sampling period) against dis-
tance from the aluminum plant. We termed
these graphs “Radial Profiles.” These specific
radii were selected for discussion because: 1)
they are representative of all radii, and 2)
they extend into Glacier National Park. The
right ordinate depicts fluoride concentration
from 10 to 10,000 ppm, (10 ppm is the con-
trol level) and the abscissa represents distance
from the plant in miles. The data was plotted
on logarithmic paper to accentuate smaller
fluoride values. Plots located in Glacier Na-
tional Park are designated by G.N.P.
The general shape of the fluoride curve is
similar on all three radii, and similar on the
other seven radii sampled, and shows abnor-
mally high fluoride concentrations occurred
(above 10 ppm) up to 12 and 14 miles from
the reduction plant, including lands within
Glacier National Park.
To simplify interpretation of the fluoride
data, a single diagram was prepared that de-
picts virtually the entire extent of the pollu-
tion (figure 8). From the graphs of all the
radial profiles, second sampling, we inter-
preted the distance at which average plot fluo-
ride concentrations equalled the arbitrarily es-
tablished levels of 10, 15, 20, 30, 60, 100,
300, and 600 ppm. Those distances were
plotted on the radii, and then equal pollution
(fluoride concentration) levels were con-
nected by lines. These lines of equal pollution
are termed “isopols.” Data from the first
sampling gave a similar figure, as did data for
the separate vegetational categories. One can
easily see the area of fluoride “fallout” and
the various levels of average concentration.
The distribution of fluorides generally cor-
responds with the prevailing southwesterly
winds.1 The areas included within (total area
within a given isopol, including all area sus-
taining fluoride levels equal to or greater than
the given isopol) and between (the area be-
tween two given isopols, such as the area be-
tween the 30 and 60 isopols) isopols are
tabulated in Appendix III-A. Vegetation on
approximately 214,000 acres had accumu-
lated more than 10 ppm fluoride, on 69,120
acres had accumulated 30 ppm or more, and
on 7,040 had accumulated 100 ppm or more.
(The isopols southwest of Columbia Falls
were constructed from special sample data
and may not be as reliable as those estimated
from radial data. They are, however, indica-
tive of the general pattern in a southwesterly
direction.) Much vegetation in the area within
the 30 ppm isopol has been affected to vari-
ous degrees by fluorides from the aluminum
plant.
Injury Index. Injury index values were
averaged separately on a plot by plot basis for
fluoride content, irrespective of vegetation
type (Appendix II-A and II-B). However, plot
xThe Environmental Protection Agency collected
detailed information on meteorological conditions in
the area and will publish the findings soon.
12
FIGURE 4
Schematic diagram showing increasing concentration of fluorides in
vegetation in the direction of and converging at the Anaconda Aluminum.
The arrows represent the direction of increasing concentration.
13
Injury Index
14
Fluoride, PPM
Injury Index
15
Fluor i de, PPM
Injury Index
1 .000
.800
.600
. WO
.200
. 100
.080
.060
.040
.020
.010
.008
.006
.004
.002
.001
,/4,,, 12 4 6 8 10 12 14
Distance From Plant, Miles
16
Fluoride, PPM
FIGURE 8
Isopols of fluoride pollution at
Columbia Falls, Montana. 69,120
acres are included within the 30
isopol. See append i xes III A and III B
for acreage data.
10
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17
averages were determined by considering only
those samples that had an I.I. of 0.001 or
greater. Radial profiles of I.I. values were
made for all radii separately for each sampling
period. Only radii 4, 5, and 6 - figures 5, 6,
and 7, respectively were selected for inclusion
in this report, for the same reasons as outlined
in the previous section on fluoride content.
The left ordinate depicts I.I. values from
0.001 to 1.00. The abscissa represents dis-
tance in miles from the aluminum factory.
The graphs indicate a decreasing amount of
visual injury at increasing distances from the
aluminum plant. Visual injury was found up
to 8.5 miles from the factory on radius 4, up
to 12 miles on radius 5, and up to 4 miles on
radius 6. Generally, visual injury was found
on sensitive species (Western white pine,
lodgepole pine, and ponderosa pine) within
the 30 isopol.
High injury indices were nearly always as-
sociated with values of fluoride concentration
above 100 ppm. From data collected the
second sampling period, we found the average
injury index for plots 1-4, radii 3-8, was
0.142. As mentioned previously, of vegetation
collected during the second sampling period,
only conifers were analyzed for I.I. Radii 3-8
all transected a part of Teakettle Mountain,
and plots 1-3 occurred on the west face of
Teakettle Mountain. Plots No. 4 were on the
east side of Teakettle, just over the crest of
the ridge. All these plots had average fluoride
values more than 100 ppm, as indicated in
Appendixes II-A and II-B. Because the great-
est and most obvious amount of visual injury
occurred on the west face of the mountain,
we used this area as a basis for establishing the
classes of injury as shown in Table II.
Table II. — Classification of Visual Injury of
Conifers
Class
Average injury index
Non-injured
< 0.006
Light
0.007 - 0.050
Moderate
0.051 - 0.099
Severe
> 0.100
In general, conifers on most of the west
face of Teakettle Mountain have been severely
injured by fluorides; on the north face of
Columbia Mountain have sustained moderate
injury; and on the east face of Teakettle have
showed moderate injury. Vegetation,
especially ponderosa pine, within the city of
Columbia Falls has been injured moderately
to severely by fluorides.
Visual injury to vegetation between the 30
and 100 isopols was restricted primarily to
the conifers — lodgepole pine, western white
pine, whitebark pine, ponderosa pine, and
Douglas-fir. However, the forb lily of the val-
ley proved to be very sensitive to fluorides
and showed typical symptoms within the 30
isopol.
The most serious visible injury to vegeta-
tion occurred in the 19,840 acres included
within the 60 ppm isopol. In 12,800 acres be-
tween the 60 and 100 isopols, 100 percent of
the foliage of lodgepole pine showed partial
necrosis, of which 50 percent was necrotic
due to fluorides. The remaining 50 percent
had been infested by four different insect
species: sugar pine tortrix, pine needle scale,
needle sheath miner, and a needle miner (fig-
ure 9). A causal relationship was not estab-
lished between elevated fluorides and insect
infestation; however, it would seem more
than coincidental that the infestation was as-
sociated so closely with the high fluorides.
In the 5,760 acres between the 100 and
300 isopols, insects subsided to endemic
levels. However, foliage of nearly all vegeta-
tion, including shrubs, forbs, and conifers,
showed moderate fluoride burn. In 1,280
acres within the 300 and 600 isopols, foliage
of all vegetation except grasses was severely
burned (figures 10 and 11) and conifers ex-
hibited terminal dieback (figure 12).
Special Samples
Fluoride Content and I.I. Data concerning
fluoride content and injury index collected on
a total of 175 special samples were very simi-
lar to radial data collected in the same areas.
Data is shown in Appendix IV. High levels of
fluorides, up to 290 ppm, were found in the
Columbia Falls area. Moderate levels up to
86.5 ppm along with moderate foliar injury
were found on Columbia Mountain, and up to
1163 ppm were found in 1969 Douglas-fir
needles on Teakettle Mountain. Injury was
18
Figure 9. — Fluoride and insect injury on lodgepole pine from the east side of Teakettle Moun-
tain. About 50% of the needles show typical fluoride burn (1 ); the rest are infested separate-
ly by sugar pine tortrix (2); pine needle scale (3); a needle sheath miner (4); and a needle
miner (5).
19
severe on Teakettle Mountain. Fluoride levels
between 20-30 ppm in 1969 conifer tissue
were common in southwest Glacier Park.
Light to moderate foliar injury also was
found. Light fluoride accumulations between
15-20 ppm and little injury was found on the
Coram Experimental Forest, and little fluo-
ride or injury was found along the northeast
edge of Hungry Horse Reservoir.
Much of the special data was used in the
verification of isopols and the extension of
isopols southwest from the aluminum plant.
Relation Between Injury Index and Fluoride
Content
As explained previously, each sample col-
lected was subjected to both a fluoride
analysis and estimation of 1. 1. Because exces-
sive fluorides can cause injury to plant tissue,
one can hypothesize a positive correlation be-
tween fluoride level and I.I. We tested this
hypothesis by regression analysis separately
on 1969 and 1970 conifer needles and shrub
foliage. Data obtained from radial plots and
special samples were used, combining data for
both sampling periods. Results of the analysis
are shown in Appendix V. The correlation
was positive and significant at the 99 percent
level of confidence for 1969 conifer needle
tissue. The “F” ratio for slope was also highly
significant. For 1970 conifer needles and for
shrubs, the correlation was nonsignificant.
This analysis readily substantiated that for
1970 conifer tissue and for all broadleaf tissue
tested, high fluoride levels existed without
corresponding visible necrosis or burn.
Rates of Accumulation
To obtain a comparison of the relative
rates of fluoride accumulation for 1969 and
1970 coniferous tissue, accumulations in
1969 tissue were paired with accumulations in
1970 tissue sampled from the same tree. Data
collected from the radial plots and special
samples, second sampling period, were used.
The data was stratified by isopol and species
type as shown in Table III. Values given in the
table are average monthly fluoride accumula-
tions in excess of the normal 10 ppm back-
ground level. The rate for 1969 tissue was
found by dividing the total excess fluoride by
17 (total length of exposure in months) and
by 5 for 1970 tissue.
The data indicates for pines that the rate of
accumulation was about the same in 1970 as
in 1969 between the 60-600 isopols but slowed
down between the 10-60 isopols. The firs and
spruces maintained about the same rate in
1970 as in 1969 for all the isopols.
Histological Results
Definite histological reactions were found
in internal tissue of necrotic conifer needles.
As described previously a 2mm piece of needle
was taken from the “transition zone” be-
tween healthy and necrotic tissue and sec-
TABLE III
Rates of Fluoride Accumulation
Species Type 1
Pines
Firs and spruces
Isopol
1969
1970
1969
1970
300 - 600
12.69
16.26
30.16
32.26
100 - 300
16.73
8.27
24.11
15.76
60-100
4.56
7.22
30- 60
1.69
0.54
1.54
1.22
10- 30
0.67
0.45
0.94
1.58
1 "Pines” includes ponderosa, western white, whitebark, and lodgepole pines. Firs and Spruces ” includes
Douglas, grand, and subalpine firs and Engelmann spruce.
20
Figure 10. — (top) Severe foliar fluoride burn on lodgepole pine. This sample was collected in
the 300 isopol zone on U. S. Forest Service land. XO.5
Figure 11. — (bottom) Closeup of fluoride burn on lodgepole pine collected from within the
300 isopol zone on U. S. Forest Service land. X2
21
Figure 12. — Terminal dieback of Doublas-fir, caused by repeated fluoride fumigations. This
tree is within the 300 isopol zone on Forest Service land. XO.5
Figure 13. — Hypertrophied transfusion parenchyma cells and associated collapse of transfusion
tracheids (arrow). Lodgepole pine. X350.
tioned at 9 micra thickness. Microscopic ex-
amination of conifer tissue in the early stage
of necrosis (green-yellow part of transition
zone) revealed that phloem and transfusion
parenchyma and albuminous cells hyper-
trophied extensively, crushing and causing
collapse of transfusion tracheids and phloem
elements (figure 13). Enlarged nuclei were al-
ways associated with the hypertrophied cells
and expanded nuclei often occurred in meso-
phyll cells (figure 14). Often the mesophyll
cell immediately interior to the stomatal
opening had been killed before fixation and
sectioning. Epithelial tissue and nuclei hyper-
trophied extensively, often occluding resin
canals (figure 15).
In the later stage of fluorosis (necrotic por-
tion of transition zone), many of the hyper-
trophied cells had collapsed, leaving a void in
the tissue. Granulosis of the chloroplasts in
mesophyll cells was obvious.
This disease syndrome is unlike any caused
by fungi or adverse weather conditions, and is
very distinctive for fluorosis of conifer tissue.
This type of internal injury caused by fluo-
rides occurred generally within the isopols 30
ppm and greater, including vegetation in Gla-
cier National Park, but varied depending on
the species.
Aerial Photography
The aerial photography was scheduled to
be completed by June 15, 1970. However, be-
cause of adverse weather, it was not done
until mid-July, and much of the injury pres-
ent on vegetation was masked by the new
flush of growth. Even so, injury was detec-
table generally within the 60 ppm isopol.
Mortality of conifers was readily identifiable
within the 300 ppm isopol. Ektachrome Aero
film was satisfactory for delineating general
areas sustaining visual pollution injury.
23
Figure 14. — Hypertrophied nuclei in mesophyll parenchyma cells (arrows). Lodgepole pine.
X950
24
Figure 15. — Hypertrophied epithelial cells in ponderosa pine resin canal (arrow). X950.
Entomological Phase
Fluoride accumulation by Insects
Control Samples. Fluoride content data of
control insects are given in Appendix VI.
Foliage feeders were represented by larch
casebearer at 16.5 ppm and grasshoppers at
7.5 ppm. Highest control for cambial feeders
was 11.5 ppm found in Ips sp. Red turpentine
beetle, also a cambial feeder, had 4.8 ppm
fluoride. Bumblebees, which are pollinating
insects, had 7.5 ppm and damselflies, which
are predaceous, had 9.2 ppm fluoride.
Test Samples. Generally at least twice as
much fluoride was found in test samples as in
corresponding control samples. Foliage
feeders collected within the areas sustaining
fluoride pollution had from 21.3 to 48.6 ppm
fluoride, with weevils containing the highest.
From 8.5 to 52.5 ppm fluoride was found in
the cambial feeding group, with engraver
beetles sustaining the largest amount. The
highest readings in the pollinating groups were
found in bumblebees at 406 ppm and the low-
est in the wood nymph butterfly at 58.0 ppm.
Predaceous insects ranged from 6.1 to 170.0
ppm fluoride, with ants accumulating the
largest amount.
Insect Population Sampling
Controls. Larch casebearers ranged from
0 - 27.6 per 100 spur shoots (Appendix VII).
Scale counts on lodgepole pine averaged
0.3 insects per 600 needles (Appendix VIII);
on ponderosa pine they averaged 5 per 600
needles (Appendix IX).
Radial Collections. Of the possible sam-
pling locations, only 30 plots had sufficient
larch to sample larch casebearer populations;
34 plots had sufficient lodgepole pine to sam-
ple for scale insects; and 16 plots had suffi-
cient ponderosa pine to sample for scales.
Because extensive sampling of vegetation
for foliar fluoride analysis was done in the
pathological phase, we did not feel it neces-
sary to repeat vegetation collections on indi-
vidual plots during this phase. Therefore,
counts of casebearer and scale were compared
to the fluoride readings from the respective
plots in the pathological phase.
No discernible pattern existed from the
larch casebearer samples (Appendix VII). Rel-
atively high casebearer counts were found at
all distances from the aluminum plant with
the exception of one-fourth mile where the
only larch sample taken had no casebearer.
Generally, scale counts on lodgepole pine
decreased with increasing distance from the
aluminum plant, with the exception of the
8-mile samples (Appendix VIII).
Scale counts on lodgepole pine were com-
pared to foliar fluoride content of conifers on
the same plot (Appendix X). Linear regression
analysis showed no significant correlation (r =
0.201, 30 degrees of freedom) existed.
The regression line is shown in Figure 16.
A constant increase in scale numbers with in-
creasing fluoride concentrations is indicated.
Although the correlation is insignificant, the
graph does indicate a trend and more exten-
sive sampling likely would confirm the
relationship.
Lodgepole pine that had scale counts ex-
ceeding 50 per 600 needles contained 23 to
401 ppm fluoride (average 133 ppm) in all
vegetation, compared to a range of 6 to 160
ppm fluoride (average 36 ppm) for pines with
less than 50 scales per 600 needles.
The same pattern existed for the ponder-
osa pine samples (Appendix VIII) even
though the number of samples was smaller.
26
o
sa lPaaN 009/sa LB3S ^O'ON
27
Fluoride, PPM
Discussion
and
Conclusions
General
The original objectives of the evaluation
were satisfied. The chemical and histological
analyses showed definitely that fluorides were
the major factor contributing to injury and
damage on vegetation peripheral to the alumi-
num reduction plant. That the source of the
fluorides was the Anaconda Company’s alumi-
num reduction plant is confirmed by the con-
vergence of lines of increasing concentration
at the reduction plant. Through systematic
and special sampling systems, we were able to
map the area affected by fluorides.
The 32 insect tissue samples analyzed
showed definitely that fluorides accumulate
in insects. Generally, scale insects increased
with increasing concentrations of fluoride in
lodgepole and ponderosa pine needle tissue;
however, data was not complete. Larch case-
bearer populations showed no trends.
Rates of Accumulation
Previously we mentioned that the alumi-
num plant had reduced fluoride emissions
from 7,600 to 5,000 pounds per day. One can
hypothesize that a corresponding decrease in
fluroide content of vegetation should occur.
However, our data shows this is not uni-
versally true. In fact, only for the pine species
under insidious levels of fumigation (10-60
ppm isopols) did the rate drop substantially.
The rate of accumulation in firs did not
change even at the insidious levels of fumiga-
tion. We interpret this as indicating the exist-
ence of a threshold concentration of atmos-
pheric fluoride as measured by emission at the
aluminum plant, below which a decreasing
level of atmospheric fluoride results in a cor-
responding decrease in accumulation by
plants and which, when exceeded, contributes
little to the total accumulation by plants. This
threshold effect could be realized either by
short exposures to high concentrations of at-
mospheric fluorides or prolonged exposure to
lower levels. The threshold level may be much
lower than 5,000 pounds per day. Even at
“low” levels of 500 to 1,000 pounds per day,
injury to vegetation could be expected up to
3 or 4 miles from the aluminum plant, and
even farther under stable inversion periods.
Possibly the threshold for pine species was
reached somewhere between the 10-60
isopols, but was never reached for the firs and
spruces. A possible explanation for this dif-
ferential response between pines and firs is
that pines are more sensitive to fluorides than
are firs and spruces. Gordon (personal com-
munication) has indicated that the physi-
ological activity of a tree is directly related to
its ability to accumulate fluorides. Thus pine
trees sensitive to fluorides may accumulate
fluorides rapidly up to a point, at which time
phytotoxic effects result in a decrease in
physiological activity and a corresponding de-
crease in fluoride accumulation rate. Because
the fluoride concentration at which phyto-
toxicity occurs in firs and spruces may be
higher than pines, their physiological activity
would be greater and their ability to accumu-
late fluorides would continue beyond that of
pines.
Susceptibility of Species
We noted apparent differences in fluoride
susceptibility in terms of expression of visual
burn symptoms by the plant. Of the conifers,
white pines were most susceptible followed
by ponderosa pine, lodgepole pine, and
Douglas-fir, respectively. Spruces, western red
cedar, and subalpine fir were most tolerant.
Of the shrubs, chokecherry and serviceberry
showed symptoms of fluorosis quite readily,
with buffalo berry the most tolerant. Lily of
the valley and disporum were highly sensitive
compared to other forbs. These classifications
are, however, based only on field data and ob-
servations.
28
Ecological Implications
Ecologically, western white pine is re-
garded as a serai or temporary species in the
trend towards a climax community. This
species occurs on the east side of Teakettle
Mountain as an integral part of the forest
community. However, it has been severely af-
fected by fluorides, and in many cases is dy-
ing or dead. This unnatural selection most cer-
tainly is hastening the trend towards climax.
The same sort of rational could also be made
for lodgepole pine, for it too is affected by
fluorides much more severely than subalpine
fir and western red cedar. Certainly unnatural
ecological changes are occurring in response
to the fluoride pollution, are resulting in re-
duced biological diversity, and should receive
considerable study in the future.
Pollution in Glacier National Park
Vegetation within 71,670 acres of Glacier
National Park has accumulated, in quantities
greater than 10 ppm, fluorides emitted from
the reduction plant (Appendix III-B). On
9,600 acres, plants have accumulated 30 ppm
or more, and some have been lightly injured.
Plants on 371 acres showed average accumu-
lations up to 60 ppm with some moderate in-
jury on lodgepole, white, and ponderosa pines
and Douglas-fir. As indicated by figure 8,
most of the injury and high accumulation
levels occurred on the southwest face of the
Apgar Mountains and the southwest face of
the Belton Hills. No samples were collected
from the upper reaches of McDonald Creek in
Glacier National Park. However, the isopol
map does indicate the possibility of pollution
damage near Logan Pass, and future sampling
should include these areas.
Pollution in Coram Experimental Forest
All the special samples collected near
Desert Mountain (Figure 3) were located
within Coram Experimental Forest. Many
studies important to management of western
larch currently are in progress on the exper-
imental forests. Generally, average fluoride ac-
cumulations in western white pine and west-
ern larch ranged from 10-25 ppm. Little foliar
injury was found. We do not know what af-
fect these insidious fluoride accumulations
may have on reproductive potential, growth,
and other factors of the species being studied.
However, the presence of elevated fluorides
may contribute to unexplained error in sta-
tistical analyses of the data.
Study Replicated
Data for construction of isopols and radial
profiles displayed in this report were obtained
from the second sampling period as these
were more current. A similar pattern existed
for data of the first sampling period but was
not of the magnitude as that of the second.
Because data of both sampling periods was
collected in the same manner, each sampling
period could be considered a replicate of the
same experiment. As both sampling periods
yielded data showing similar trends, the tech-
niques used (i.e., radial sampling) are con-
sidered valid.
Insects and Fluoride
The damsel flies and ostomids are 100 per-
cent predatory in both larval and adult stages.
Fluoride accumulated in these insects must
have come from the insects upon which they
fed, indicating that fluoride is passed along
the food chain to some predators.
In two instances where both larvae and
adults of the same species (flatheaded beetles
and ostomids) were analyzed, accumulation
was much higher in the adults. Bumblebees
collected in the summer had over twice the
fluoride levels as those collected in the spring.
Both cases suggest that accumulation occurs
throughout the life of the insects.
Many plants are dependent upon insect
pollinators for seed production. By altering
the pollinator complex, i.e., bumblebees,
honeybees, sphinx moths, and others, it is
possible to alter vegetational types, and subse-
quently much of ecology of an area. Studies
have shown fluorides to be devastating to
honeybees. If this applies to pollinators in
general it could have a detrimental effect on
fruit trees, legumes, and many other insect-
pollinated flowering plants in the polluted
area.
Current research shows that several chemi-
cals and pesticides (DDT, etc.) are adversely
affecting organisms farther up the food chain.
Eagles lay soft-shelled nonviable eggs due to
feeding on fish containing high levels of DDT.
Insects are one of the most important ele-
ments of the food chain. They are the only
29
watershed through loss of ground cover likely
is minimal.
Previous research has shown that livestock
will develop fluorosis if feeding is done on
vegetation containing more than 35 ppm fluo-
ride. The area within the 30 isopol contains
several thousand acres of grazing lands that
should not be utilized, indicating a dollar
value which can be fixed.
Research also has shown that diameter
growth rates of conifers will decrease from"
1-6 fold in fluoride polluted areas. We have
not collected at Columbia Falls any data con-
cerning growth decline of conifers. However,
the decrease mentioned above could be ap-
plied to commercial species in the area.
Environmental damage is continuing and
can be stopped only by (1) installation of effi-
cient pollution abatement equipment at the
reduction plant to limit fluoride emission to
0.0 pounds per day, which likely is impossi-
ble, or (2) closure of the plant. The latter is
an unrealistic position because the aluminum
plant does provide jobs to hundreds of people
at a payroll exceeding $9 million per year.
Therefore, it would seem appropriate to sup-
port the fluoride emission standard of 864
pounds per day set by the State of Montana.
If emissions are not reduced to the State
standard, extensive pollution can be expected
to continue. As a result, it would be unwise to
raise livestock within the area included by the
30 ppm isopol. Leafy vegetables and fruits
grown or collected within the 30 ppm isopol
should be thoroughly washed before they are
eaten.
Forest vegetation would continue to de-
cline, and the southwestern portion of Glacier
National Park would continue to sustain a
chronic level of injury caused by excessive
fluorides.
food of some birds, fish, amphibians, reptiles,
mammals, and arthropods including other in-
sects and arachnids. If fluorides accumulated
by insects are injurious to insectivorous ani-
mals, then additional damage may be
occurring.
It should be remembered that while there
are many undesirable insects we would like to
control, only about one in 100 is considered
to cause significant crop loss. Much research is
needed before the effect of different levels of
atmospheric fluoride upon insect populations
is clearly understood.
Fluroide has not been reported to be trans-
located in conifers, it is said to accumulate in
the foliage by absorption. The bark beetle
species examined feed solely as larvae and
adults on the cambium of conifers. The high
fluoride readings in some bark beetle samples
indicate that fluorides are translocated in the
xylem or phloem of the tree and are accessi-
ble to bark beetles.
Scale insects are known to build up on
weakened or disturbed trees. Excessive dust
alone can trigger scale outbreaks. There ap-
pears to be a relationship to scale populations
and fluoride accumulated by the vegetation,
but more extensive sampling is needed.
Economic and Esthetic Damage
The Forest Service is charged with the re-
sponsibility of wise use of all National Forest
lands. We are also responsible for technical ad-
vise and service to National Parks, State and
private concerns. The responsibilities are ad-
ministered in five general use categories: 1)
wildlife, 2) water, 3) forage, 4) recreation,
and 5) timber. Therefore, an economic analy-
sis of fluoride pollution would have to con-
sider values in all these categories.
We have not yet made a thorough eco-
nomic analysis of the fluoride pollution prob-
lem at Columbia Falls. Recreation and wild-
life values are difficult to establish. Gordon1
has shown that wildlife in the area is accumu-
lating fluorides, but no economic loss has
been established. Excessive fluoride concen-
trations in water have not yet been reported
in the Columbia Falls area, and damage to the
1 Personal communication with Dr. C. C. Gordon,
University of Montana.
Future Plans
We are establishing a permanent system to
monitor for fluoride pollution in the Colum-
bia Falls area. The precise methods have not
yet been outlined.
During the summer of 1971 we will evalu-
ate possible timber growth losses due to fluo-
ride. It is anticipated that a series of variable
plots would provide the data, but definite
procedures have not yet been established.
30
Acknowledgements
Special appreciation is extended to person-
nel of the Flathead National Forest, especially
Mr. John Ulrich, for assistance in organization
of the field part of this study; to Mrs. Carma
Gilligan for her excellent histological work; to
Mr. Ralph E. Williams for valuable assistance
in organizing the manuscript, and to many
other close associates who aided in the field
work and reviewed the manuscript. We also
wish to extend our gratitude to Mrs. Karen
Brown, who typed the manuscript.
31
Literature
Cited
Adams, Donald F., C. Gardner Shaw, Richard
M. Gnagy and others.
1956. Relationship of atmospheric fluo-
ride levels and injury indexes on Gladiolus
and ponderosa pine. Agricultural and Food
Chemistry 4(1): 64-66.
Anonymous.
1969. Tentative Method of analysis for
Fluoride content of the atmosphere and
plant tissue. Health Laboratory Science, 6:
84-101.
Bousfield, W. E.
1969. Sampling plan for larch casebearer.
USDA For. Serv., Div. State & Pri. For-
estry, Missoula, MT. Unpub. rept.
Caparrini, W.
1957. Fluorine poisoning in domestic ani-
mals (cattle) and bees. Zooprofilass 12:
249-250.
Carlson, C. E. and J. E. Dewey.
1970. Study plan for the evaluation of flu-
oride damage to ecosystem segments on
National Forest land in the vicinity of Co-
lumbia Falls, MT. USDA For. Serv., Div.
State & Private Forestry, Missoula, MT.
Compton, O. C., L. F. Remmert, J. A.
Rudinsky and others.
1961. Needle scorch and condition of
ponderosa pine trees in The Dalles area.
Misc. paper 120, Agri. Exp. Sta., Oregon
State Univ., Corvallis, OR.
Daubenmire, R., and J. B. Daubenmire.
1968. Forest Vegetation of Eastern
Washington and Northern Idaho. Wash-
ington Agr. Exp. Sta. Tech. Bull. 60.
Fischer, G. W.
1950. Second progress report Spokane
County ponderosa pine blight investi-
gation. USDA For. Serv., Unpub. rept.
Gordon, C. C.
1970. Damage to Christmas trees near
Oakland, Maryland, and Mountain Storm,
West Virginia. Univ. of Montana, Missoula,
MT., special report.
1969. Cominco American Report II. Univ.
of Montana, Missoula, MT.
Guilhon, J., R. Truhaut, and J. Bernuchon.
1962. Studies on the variations in fluorine
levels in bees with respect to industrial at-
mospheric air pollution in a Pyrenean vil-
lage. Acad. d’Agr. de France, Compt.
Rendt. 48: 607-615.
Hickey, H. R.
1968. Controlling aluminum effluent re-
duction. System Services Resources Re-
search, Inc. Sub. of Hazelton Laboratories,
Inc. TRW Life Sciences Center.
Hindawi, I. J.
1970. Air pollution injury to vegetation.
U. S. Dept. HEW, Natl. Air Pollution Con-
trol Adminis., Raleigh, NC., pp. 26-29.
32
Jacobson, Jay S., Leonard H. Weinstein, D. C.
McCune, and A. E. Hitchcock.
1966. The accumulation of fluorine by
plants. J. Air Poll. Cont. Assoc. 16 (8):
412-417.
Johnson, P. C.
1950. Entomological aspects of the pon-
derosa pine blight study, Spokane, WN.
USDA For. Serv. Unpubl. Rept.
Lezovic, J.
1969. The influence of fluorine com-
pounds on the biological life near an alumi-
num factory. Fluoride Quarterly Rept.,
vol. 2, No. 1.
Lynch, Donald W.
1951. Diameter growth of ponderosa pine
in relation to the Spokane pine-blight
problem. Northwest Science 25: 157-163.
MacLean, D. C., R. E. Schneider, and L. H.
Weinstein.
1969. Accumulation of fluoride by forage
crops. Contrib. Boyce Thompson Inst. 24
(7): 165-166.
Marier, J. R.
1968. Fluoride research. Science 159:
1494-1495.
Marier, J. R., Dyson Rose, and J. S. Hart.
1969. Environmental fluoride. Pollution
Task Force Rept. Div. of Biology, N.R.C.,
Ottawa.
Maurizio, A., and M. Staub.
1956. Poisoning of bees with industrial
gasses containing fluorine in Switzerland.
Schweiz. Bieren Ztg. 79: 476-486.
Outram, I.
1970. Some effects of fumigant sulphryl
fluoride on the gross metabolism of insect
eggs. Fluoride Quarterly Rept. vol. 3,
No. 2.
Semrau, Konrad T.
1957. Emission of fluorides from indus-
trial processes — a review. J. of Air Poll.
Cont. Assoc., 7: 92-108.
Shaw, Charles Gardner, George W. Fischer,
Donald F. Adams, and Mark F. Adams.
1951. Fluorine injury to ponderosa pine.
Phytopath. 4a: 10, p. 943, abs.
Solberg, R. A. and D. F. Adams.
1956. Histological responses of some plant
leaves to hydrogen fluoride and sulfur
dioxide. Amer. J. Bot. 43: 755-760.
Stark, R. W., P. R. Miller, R. W. Cobb, Jr.,
and others.
1968. Photochemical oxidant injury and
bark beetle (Coleoptera: Scolytidae) infes-
tation of ponderosa pine. Hilgardia, 39 (6).
Thomas, M. D.
1961. Effects of air pollution on plants.
World Health Organization Monograph Se-
ries 46.
Treshow, M., Franklin K. Anderson, and
Frances Harner.
1967. Responses of Douglas fir to elevated
atmospheric fluorides. For. Science 13(2):
114-120.
33
Appendix I
COMMON AND SCIENTIFIC NAMES OF PLANTS AND
ANIMALS STUDIED OR REFERRED TO IN THIS REPORT
TREES
Common Name
Western Larch
Western White Pine
Whitebark Pine
Ponderosa Pine
Douglas-fir
Lodgepole Pine
Engelmann spruce
Grand fir
Western Red Cedar
Subalpine fir
Yew
Juniper
SHRUBS
Service berry
Oregon grape
Ribes
Snowberry
Ocean Spray
Buffalo Berry
Spiraea
Paper Birch
Rose
Mountain maple
Willow
Dogwood
Cottonwood
Huckleberry
Scientific Name
Larix occidentalis Nutt.
Pinus monticola Dough ex. D.
Pinus albicaulis Engelm.
Pinus ponderosa Laws.
Pseudotsuga menziesii (Mirbel) Franco
Pinus contorta var. latifolia Engelm.
Picea engelmannii Parry ex Engelm.
Abies grandis (Dough) Lindl.
Thuja plicata Donn. Hort.
Abies lasiocarpa (Hook.) Nutt.
Taxus brevifolia Nutt.
Juniperus occidentalis Hook.
Amelanchier alni folia Nutt.
Berberis repens Lindl.
Ribes sp. L.
Symphoricarpos albus (L). Blake
Holodiscus discolor (Pursh) Maxim.
Shepherdia argentea (Pursh) Nutt.
Spiraea betulifolia Pall.
Betula papyrifera Marsh.
Rosa woodsii Lindl.
Acer glabrum Torr.
Salix sp. L.
Cornus canadensis L.
Populus trichocarpa T. and G. ex Hook
Vaccinium sp. L.
34
Common Name
Scientific Name
Mountain ash
Ninebark
Aspen
Alder
Chokecherry
Red stem ceanothus
Evergreen Ceanothus
Pachistima
Hawthorne
Honeysuckle
Elderberry
Kinnikinnick
Syringa
FORBS
Lily of the Valley
Lupine
Mullein
Heart Leaf Arnica
Strawberry
Thimbleberry
Fern
Wild Snapdragon
Hawkweed
Fireweed
Yarrow
Mint
Larkspur
Arrow Leaf Balsam Root
Wild Pea
Devils Club
Aster
Meadow Rue
False Azalea
Bedstraw
Goldenrod
Wild Onion
Lousewort
Canadian Thistle
Disporum
Absinthium
Raspberry
Pussytoes
Michaux sagebrush
Hounds Tongue
Alum Root
Dogbane
Sorbus scopulina Greene
Physocarpus malvaceus (Greene) Kuntze
Populus tremuloides Michx.
Alnus incana (L.) Moench
Prunus virginiana L.
Ceanothus sanguineus Pursh
Ceanothus uelutinus Dougl. ex Hook.
Pachistima myrsinites (Pursh) Raf.
Crataegus douglasii Lindl.
Lonicera ciliosa (Pursh) DC.
Sambucus cerulea Raf.
Arctostaphylos uua-ursi (L.) Spreng.
Philadelphus lewisii Pursh
Smilacina stellata (L.) Desf.
Lupinus Sp. L.
Verbascum thapsus L.
Arnica cordi folia Hook.
Fragaria virginiana Duchesne
Rubus parviflorus Nutt.
Pteridium equilinum (L.) Kuhn
Antirrhinum sp. L.
Hieracium sp. L.
Epilobium angustifolium L.
Anchillea millefolium L.
Mentha sp. L.
Delphinium sp. L.
Balsamorhiza sagittata (Pursh) Nutt.
Vicia sativa L.
Oplopanax horridum (J. E. Smith) Miq.
Aster sp. L.
Thalictrum occidentale Gray
Rhododendron sp. L.
Galium sp. L.
Solidago sp. L.
Allium sp. L.
Pedicularis sp. L.
Cirsium arvense L. (Scop.)
Disporum hookeri (Torr.) Nicholson
Artemisia absinthium L.
Rubus idaeus L.
Antennaria sp. Gaertn.
Artemesia michauxiana Bess.
Cynoglossum officinale L.
Heuchera sp. L.
Apocynum androsaemifolium L.
35
GRASSES
Common Name
Scientific Name
Pine Grass
Bear Grass
Timothy Grass
Cheat Grass
Blue Grass
Calamgrostis rubescens Buckl.
Xerophyllum tenax (Pursh) Nutt.
Phleum sp. L.
Bromus tectorum L.
Poa sp. L.
INSECTS
Black pine leaf scale
Desert Locust
Yellow Meal Worm
Larch case bearer
Pine Needle Scale
Sugar pine tortrix
Needle Sheath Miner
Needle Miner
Bumblebee
Sphinx moth
Honey bee
Skipper butterfly
Wood nymph
Weevils
Grasshoppers
Cicadas
Engraver beetles
Buprestid larvae
Buprestid adults
Red Turpentine Beetle
Douglas-fir Beetle
Ants
Ostomids
Damsel Flies
Longlegged fly
Cerambycids
Elaterids
Nuculaspis californica (Coleman)
Schistocera gregaria (Forsk.)
Tenebrio molitor (L.)
Coleophora laricella (Hbn.)
Phenacaspis pinifoliae (Fitch)
Choristoneura lambertiana (Busck)
Zellaria hambachi Busck
Recurvaria sp.
Bombus sp.
Hemaris sp.
Apis me lli f era Linn.
Erynnis sp.
Cercyonis sp.
Magdalis sp.
Melanoplus sp.
Family Cicadidae
Ips sp. DeGeer
Melanophila sp.
Melanophila sp.
Dendroctonus valens LeConte
Dendroctonus pseudotsugae Hopk.
Family Formicidae
Temnochila sp.
Argia sp.
Medeterus sp.
Family Cerambycidae
Family E later idae
MAMMALS
Columbian-ground squirrel
Grizzly Bear
Elk
Spermophilus columbianus columbianus Ord
Ursus horribilis Merriam
Cervus canadensis Nelsoni Bailey
36
Appendix IIA
TABULATION OF RADIAL AND CONTROL DATA
First Sampling
Average Fluoride Content I. I.
Plot#
Shrubs
Conifers
1969 1970
Herbs
Grasses
Grand
Ave
Ave
I. I.
High
I. I.
Control #1
5.651
6.25
9.25
6.67
-
6.92
.003
.006
Control #2
5.0
3.5
7.5
5.0
1.3
4.79
0.0
0.0
Control #3
11.4
7.58
6.28
10.0
9.8
8.02
0.0
0.0
Control #4
7.5
10.0
11.0
8.5
8.5
10.36
0.0
0.0
Control #5
7.17
4.75
6.77
12.0
-
7.03
.007
.014
Control #6
4.77
6.33
3.00
5.50
16.0
5.80
.005
.006
Rl-Pl2
108.5
300
40.8
188
70.0
122.36
.138
.235
R1-P2
106.5
107.8
18.3
-
45.0
70.72
.305
.442
R1-P3
48.8
42.2
11.4
-
18.8
31.94
.044
.090
R1-P4
19.8
18.3
14.7
12.5
2.5
15.46
.132
.301
R1-P5
17.0
--
-
16.0
8.0
12.88
0.0
0.0
R1-P6
3.0
12.5
9.0
-
4.0
8.94
0.0
0.0
R1-P7
6.3
5.8
9.3
-
4.0
6.80
0.0
0.0
R2-P1
42.4
143.5
17.5
93.8
66.3
91.21
.075
.313
R2-P2
112.7
127.5
20.0
90.0
83.3
89.59
.196
.528
R2-P3
44.3
77.9
17.8
50.0
49.0
50.21
.163
.313
R2-P4
13.2
20.7
8.83
-
13.0
14.71
.079
.200
R2-P5
13.0
9.5
17.3
9.0
32.0
15.86
.012
.019
R2-P6
3.6
5.5
2.3
5.5
2.5
3.70
0.0
0.0
R2-P7
7.1
8.9
9.2
7.3
6.0
8.13
.004
.008
1 Fluoride content, ppm, dry weight basis
2R = Radius No., P = Plot No.
37
APPENDIX II-A, Con’t
Average Fluoride Content I. I.
Plot#
Shrubs
Conifers
1969 1970
Herbs
Grasses
Grand
Ave
Ave
I. I.
High
I. I.
R3-P1
1166.6
-
-
875.5
775
1004.3
.020
.027
R3-P2
488
637
229
315
344
411.3
.107
.271
R3-P3
149.0
-
-
115
3.0
118.6
.009
.021
R3-P4
100.0
96.0
16.0
-
82.5
78.90
.136
.136
R3-P5
37.2
31.5
11.5
--
22.5
26.31
.066
.334
R3-P6
10.0
10.8
10.9
--
2.1
9.23
0.0
0.0
R3-P7
14.5
7.0
8.0
3.3
8.20
0.0
0.0
R4-P1
704.2
—
--
628.0
156
604.14
.025
.076
R4-P2
778.0
-
-
450.5
231
537.60
.010
.063
R4-P3
425.5
681.5
116.5
525
206
397.25
.072
.500
R4-P4
120.0
198.4
65.1
96.5
234
130.23
.150
.470
R4-P5
21.2
57.2
15.3
34.5
49.0
38.16
.066
.215
*R4-P6
14.0
9.77
7.50
10.0
13.0
10.13
.003
.007
*R4-P7
13.7
17.8
6.83
17.8
-
13.25
.038
.051
*R4-P8
15.4
18.0
7.15
9.9
103
19.68
.003
.003
*R4-P9
8.0
11.2
6.0
15.5
71.5
16.98
0.0
0.0
*R4-P10
9.27
8.93
4.0
5.7
5.8
6.88
.008
.008
R5-P1
1719
—
-
1038
250
1181.5
.288
.580
R5-P2
653
--
--
375
600
597.8
.029
.029
R5-P3
173.7
341.0
45.0
281
444
224.2
.197
.343
R5-P4
137.5
243.7
68.6
70.0
87.5
130.7
.086
.392
R5-P5
25.0
45.9
9.60
22.5
6.0
27.80
.151
.344
R5-P6
20.0
30.2
12.7
-
21.0
19.93
.007
.023
R5-P7
16.3
30.5
-
11.5
23.5
19.60
.003
.006
*R5-P8
20.50
19.15
10.2
21.0
26.0
17.43
.006
.011
*R5-P9
20.25
29.75
11.0
13.5
72.5
24.33
.115
.115
* R5-P10
11.05
10.1
4.10
8.28
5.5
7.46
0.0
0.0
R6-P1
—
1950
-
363
313
875.3
.202
.442
R6-P2
1125.3
-
-
431
581
877.6
.019
.089
R6-P3
115.3
292
29.8
163
68.8
138.2
.019
.083
R6-P4
57.0
85.0
33.0
63.3
36.0
51.17
.106
.209
R6-P5
33.8
20.6
7.5
29.2
24.5
23.0
.073
.146
R6-P6
17.1
37.5
8.5
20.8
37.0
21.4
0.0
0.0
R6-P7
7.5
19.0
10.5
11.0
15.0
11.75
0.0
0.0
*R6-P1Q
14.65
13.5
6.0
18.5
51.5
17.83
0.0
0.0
R7-P1
1073
-
--
600
338
871.7
.065
.299
R7-P2
881.3
--
--
103
233
596.0
.118
.230
38
APPENDIX II-A, Con’t
Average Fluoride Content I. I.
Plot#
Shrubs
Conifers
1969 1970
Herbs
Grasses
Grand
Ave
Ave
I. I.
High
I. I.
R7-P3
65.3
168
22.3
62.5
75.0
68.67
.091
.225
R7-P4
55.0
111.0
18.9
44.0
44.0
63.20
.058
.111
R7-P5
25.3
-
-
25.5
42.0
29.50
0.0
0.0
R7-P6
4.8
16.2
5.3
14.0
20.5
10.87
.016
.029
R7-P7
17.3
10.0
4.5
7.0
21.0
12.43
0.0
0.0
R8-P1
399.8
975
175
-
110
409.8
.052
.115
R8-P2
129
245
136.5
235
65.0
152.3
.016
.046
R8-P3
83.3
119.8
22.5
150
-
85.9
.176
.400
R8-P4
25.3
49.0
12.7
41.5
14.3
29.4
.087
.152
R8-P5
20.0
31.8
9.8
14.0
8.0
17.2
.018
.049
R8-P6
21.5
14.9
16.0
18.3
-
17.8
0.0
0.0
R8-P7
11.8
14.2
9.2
13.3
22.5
12.6
.016
.018
R9-P1
108.7
110
39.5
51.5
41.0
70.97
.026
.026
R9-P3
26.1
--
10.0
15.0
13.5
20.40
0.0
0.0
R9-P4
43.4
68.7
24.0
-
23.5
45.31
.005
.005
R9-P5
12.5
7.8
11.0
--
6.0
9.80
0.0
0.0
R9-P6
11.4
9.3
5.37
6.5
9.5
7.72
0.0
0.0
R9-P7
5.6
9.0
10.3
25.0
5.0
9.98
0.0
0.0
R10-P1
76.5
133
42.5
31.0
38.5
66.3
.032
.097
R10-P2
43.3
61.0
14.5
45.0
22.5
38.2
•’.070
.091
R10-P3
23.3
28.8
6.3
20.8
8.5
18.9
.013
.022
R10-P4
22.8
20.8
9.3
-
16.0
16.82
.054
.054
R10-P5
15.0
23.9
7.8
10.0
7.5
15.0
0.0
0.0
R10-P6
11.4
11.5
10.8
-
10.0
10.8
.003
.003
R10-P7
6.8
9.2
3 5
11.0
6.5
7.54
0.0
0.0
* — Located on Glacier National Park lands.
39
Appendix II-B
TABULATION OF RADIAL AND CONTROL DATA
Second Sampling
Average Fluoride Content I.I.
Plot#
Shrubs
Conifers
1969 1970
Herbs
Grasses
Grand
Ave
Ave
I. I.
High
I. I.
Control #1
8.7
8.5
4.5
10.0
11.5
8.67
0.0
0.0
Control #2
6.8
7.0
5.8
10.5
5.5
6.88
0.0
0.0
Control #3
15.8
11.3
4.75
6.5
7.5
7.91
0.0
0.0
Control #4
10.9
5.9
5.2
17.0
17.0
9.74
0.0
0.0
Control #5
10.5
7.8
5.2
-
16.0
8.50
0.0
0.0
Control #6
5.7
6.0
4.8
10.0
12.5
6.46
0.0
0.0
Rl-Pl
323
338
115
310
139
258
.079
.086
R1-P2
140.5
131.7
38.9
115
102
95.3
.052
.143
R1-P3
65.5
40.7
19.3
32.0
20.0
40.9
.003
.003
R1-P4
43.3
18.5
12.8
43.5
20.5
23.4
.024
.024
R1-P5
11.5
9.0
6.0
-
5.0
8.60
0.0
0.0
R1-P6
13.8
9.10
6.2
-
-
9.06
0.0
0.0
R1-P7
9.0
4.5
5.5
--
5.0
5.90
0.0
0.0
R2-P1
136
189
64.7
61.5
93.5
111.0
.063
.093
R2-P2
147.5
100.8
26.8
146
44.5
92.6
.211
.279
R2-P3
110.0
124.7
32.8
104
32.0
85.3
.093
.104
R2-P4
29.1
17.3
8.5
-
18.5
22.2
0.0
0.0
R2-P5
16.0
16.0
9.5
14.5
-
13.6
.018
.032
R2-P6
9.0
9.3
8.5
16.0
8.8
9.48
0.0
0.0
R2-P7
9.8
8.5
5.5
8.8
4.5
7.84
0.0
0.0
40
APPENDIX II-B, Con’t
Average Fluoride Content 1. 1.
Plot#
Shrubs
Conifers
1969 1970
Herbs
Grasses
Grand
Ave
Ave
I. I.
High
I. I.
R3-P1
1194
488
258
794
600
754.7
.281
.348
R3-P2
475
496.5
367.8
463
101
401.2
.313
.628
R3-P3
281.5
294.5
70.0
137
168
199.6
.156
.313
R3-P4
130
85.5
23
107
68
90.6
.034
.043
R3-P5
49.8
42.8
17.5
36.5
31.5
33.9
.014
.025
R3-P6
15.0
11.8
7.5
5.5
12.5
11.0
.008
.015
R3-P7
7.3
12.5
10.0
7.5
4.5
8.2
0.0
0.0
R4-P1
925
-
--
1250
469
903.2
-
--
R4-P2
1244
-
--
638
205
832.8
-
--
R4-P3
900.5
390.3
87.5
363
385
432.8
.208
.495
R4-P4
211.5
286.3
123.2
375
153
215.8
.119
.301
R4-P5
47.5
53.3
22.2
11.5
20.0
35.3
.075
.211
*R4-P6
32.5
11.7
9.3
15.5
--
17.5
0.0
0.0
*R4-P7
21.3
11.0
9.7
23.5
14.5
15.3
.007
.007
*R4-P8
37.8
22.3
8.0
13.5
--
20.0
.003
.003
*R4-P9
14.3
9.8
6.3
10.5
51.5
15.3
0.0
0.0
*R4-P10
10.5
6.2
6.1
5.5
4.3
6.3
.005
.005
R5-P2
1300
--
--
875
200
918.7
--
--
R5-P3
294.5
537.5
80.3
--
508
332.2
.132
.250
R5-P4
202.5
228.7
55
111
128
160.0
.063
.114
R5-P5
59.5
56.5
23.3
270
51.0
66.91
.014
.014
R5-P6
38.0
35.0
11.7
59.5
32.0
30.3
.003
.003
R5-P7
39.0
28.5
10.0
34.0
19.5
28.3
0.0
0.0
*R5-P8
73.0
18.0
13.0
-
23.5
24.5
0.0
0.0
*R5-P9
69.0
24.8
14.2
32.5
22.0
26.9
.014
.019
*R5-P10
12.8
11.9
10.2
9.0
15.5
11.6
0.0
0.0
R6-P1
1433
1728
775
2100
469
1339
.150
.150
R6-P2
1889
-
--
3000
488
1831
--
-
R6-P3
169.5
239.6
44.7
171
117
148
.114
.144
R6-P4
64.2
140
76.3
113
53.0
83.8
.182
.291
R6-P5
67.3
27.0
10.3
47.0
27.5
36.7
.006
.006
R6-P6
54.0
32.5
13.8
14.0
21.0
32.2
0.0
0.0
R6-P7
14.8
18.8
9.8
23.5
27.5
17.2
0.0
0.0
*R6-P10
20.5
18.5
9.3
30.5
154
30.9
0.0
0.0
R7-P1
1509
-
-
700
375
1120
-
-
R7-P2
969
1825
413
56.0
293
754.2
.289
.567
* — Located on Glacier National Park lands.
41
APPENDIX II-B, Con’t
Average Fluoride Content I. I.
Plot#
Shrubs
Conifers
1969 1970
Herbs
Grasses
Grand
Ave
Ave
I. I.
High
1. 1.
R7-P3
154.5
142.5
31.3
143
160
120.0
.105
.154
R7-P4
100.5
104.7
17.5
—
63.5
76.7
.064
.064
R7-P5
47.3
51.5
20.5
28.5
16.5
25.3
.042
.042
R7-P6
35.0
37.8
18.9
25.0
13.0
26.2
.004
.005
R7-P7
23.0
14.0
10.2
17.2
7.5
14.3
.002
.002
R8-P1
812.5
906
306
750
131
619.7
0.0
0.0
R8-P2
475.5
313
209.5
325
70.0
269.9 •
0.0
0.0
R8-P3
199.0
167.0
41.3
250
97.5
145.2
.042
.067
R8-P4
48.5
56.0
55.3
32.5
—
49.3
0.0
0.0
R8-P5
33.5
28.1
14.5
31.5
14.5
24.1
0.0
0.0
R8-P6
26.3
15.5
8.8
14.5
42.5
19.5
0.0
0.0
R8-P7
16.2
14.0
8.50
—
12.5
12.7
0.0
0.0
R9-P1
251.5
168
76
198
85
171.7
0.0
0.0
R9-P2
134.7
—
—
113
132
129.8
—
—
R9-P3
45.0
19.3
12.3
52.5
35.0
30.1
0.0
0.0
R9-P4
68.0
41.5
14.0
35.8
33.0
39.0
0.0
0.0
R9-P5
9.0
4.5
4.75
8.5
6.0
5.79
0.0
0.0
R9-P6
17.3
4.7
4.27
14.0
—
9.48
0.0
0.0
R9-P7
10.5
4.0
6.03
—
5.5
6.29
0.0
0.0
R10-P1
185.5
140
62.0
200
76.0
141.5
.030
.030
R10-P2
107.7
51.5
23.5
77.5
72.5
78.3
0.0
0.0
R10-P3
30.7
23.0
8.8
26.0
28.5
24.6
0.0
0.0
R10-P4
41.8
16.5
15.5
31.0
24.0
26.6
0.0
0.0
R10-P5
9.5
20.8
10.5
33.8
12.5
17.41
.004
.004
R10-P6
—
12.3
5.0
—
11.0
10.1
0.0
0.0
R10-P7
—
4.7
4.4
7.0
8.0
5.74
0.0
0.0
42
AREA POLLUTED BY FLUORIDES, ALL LANDS STUDIED
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43
The area Southwest of Columbia Falls.
Total area sustaining greater than a given level of fluoride, p.p.m.
Area between established Isopols, i.e., the area between the 10 and 15 Isopols, etc.
Appendix III-B
AREA POLLUTED BY FLUORIDES
GLACIER NATIONAL PARK1
Area
Isopol Area Greater Between Isopols
Sq.
Sq.
Miles
Acres
Miles
Acres
10
112
71,670
40
25,600
15
72
46,080
40
25,600
20
32
20,480
17
10,880
30
15
9,600
14.42
9,229
60
.58
371
1 All lands studied in Glacier National Park were within the radial system.
44
FLUORIDE CONTENT AND INJURY INDEX VALUES
FOR SPECIAL SAMPLES
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Hungry Horse 13a* Lodgepole Pine 70 2.0
Reservoir 13b* Lodgepole Pine 69 12.0
APPENDIX IV, Con’t
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49
Appendix V
REGRESSION ANALYSES OF FLUORIDE
ON INJURY INDEX'
Shrubs
Conifers
1969
1970
n
60
130
67
Slope
-.002318
.0001297
.0001038
Y - Intercept
2.461
.122416
.0692
F - Ratio for Slope
.5136
10.9345
.970
Significance of F - ratio
N.S.2
H.S.3
N.S.
Correlation
-.094
.2805
.1213
Significance of Correlation
N.S.
H.S.
N.S.
1 Data from first sampling period only
2 N.S. — Non significant , 95 percent level.
2 H.S. — Highly significant, 99 percent level.
50
Appendix VI
FLUORIDE ACCUMULATION LEVELS IN INSECTS
Insect
Date Collected
PPM* Fluoride
Pollinators:
Bumblebee — Bombus sp.
August 12, 1970
406.0
Bumblebee — Bombus sp.
June 1, 1970
194.0
Sphinx moth — Hemaris sp.
June 1, 1970
394.0
Honey bee — Apis mellifera
June 1, 1970
221.0
Skipper butterfly — Erynnis
August 12, 1970
146.0
Wood nymph butterfly — Cercyonis sp.
August 12, 1970
58.0
Foliage feeders:
Weevils — Mixed curculionids
June 1, 1970
48.6
Grasshoppers — Melanoplus sp.
August 12, 1970
31.0
Larch Casebearer — Coleophora laricella
June 1, 1970
25.5
Cicadas — Cicadidae
June 1, 1970
21.3
Cambium Feeders:
Engraver beetles — Ips sp.
Flathead beetle
October 9, 1970
52.5
Mixed buprestids
Red turpentine beetle —
June 1, 1970
20.0
Dendroctonus valens LeConte
June 1, 1970
11.5
Douglas-fir beetle —
Dendroctonus pseudotsugae Hopk.
Flatheaded beetle larvae —
October 9, 1970
9.4
Mixed buprestids
October 9, 1970
8.5
Predators:
Ants
June 1, 1970
170.0
Ostomids — Temnochila sp.
June 1, 1970
53.4
Damsel flies — Argia sp.
June 1, 1970
21.7
Longlegged fly — Medeterus sp.
October 9, 1970
10.2
Ostomid larvae
October 9, 1970
6.1
Miscellaneous Insects:
Long horned beetles
Mixed Cerambycids
August 12, 1970
47.5
Click beetles
Mixed elaterids
June 1, 1970
36.0
Black Scavanger
Cerambycid
June 1, 1970
18.8
*PPM = parts per million by dry weight
51
APPENDIX VI, Con’t
CONTROL INSECT SAMPLES
Insect
Date Collected
PPM* Fluoride
Larch casebearer
June 1, 1970
16.5
Bark beetle — Ips sp.
October 9, 1970
11.5
Honey bees
June 1, 1970
10.5
Damselflies
June 1, 1970
9.2
Grasshoppers
August 12, 1970
7.5
Bumblebees
June 1, 1970
7.5
Barkbeetles — Dendroctonus ualens
June 1, 1970
4.8
Flathead beetles
June 1, 1970
3.5
52
Appendix VII
LARCH CASEBEARER PER 100 SPURS SAMPLED
Miles
Radii
plant
1
2
3
4
5
6
7
8
9
10
Ave.
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0
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Checks: No. 1 - 8.6; No. 2 = 0; No. 3 = 0; No. 4 = 27.6
53
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55
*70 = 1970 Foliage
Appendix X
“REGRESSION ANALYSIS OF PINE NEEDLE SCALES ON FLUORIDE CONTENT”
Y X
Radius
Plot Number
Number of Scales
Fluoride Content
1
3
1
40.7
4
55
18.5
5
0
9.0
7
26
4.5
2
2
1085
100.8
3
4
124.7
4
10
17.3
5
0
16.0
7
2
8.5
3
2
140
496.5
3
220
294.5
4
28
85.5
5
0
42.8
4
4
99
286.3
5
0
53.3
7
0
11.0
5
4
0
228.7
5
138
56.5
7
272
28.5
6
4
10
140
5
0
27.0
7
9
18.8
7
5
57
51.5
7
0
14.0
56
APPENDIX X, Con’t
Radius
Plot Number
Y
X
Number of Scales
Fluoride Content
8
4
0
56.0
5
2
28.1
7
0
14.0
9
4
0
41.5
7
0
4.0
10
5
1
20.8
7
0
4.7
Linear Regression Analysis
Y = A+BX
A = 42.036
B = 0.365
Correlation Coefficient = .201 N.S.1
1 Nonsignificant
57
The Forest Service of the U.S. Department of
Agriculture is dedicated to the principle of
multiple use management of the Nation's forest
resources for sustained yields of wood, water,
forage, wildlife and recreation. Through forestry
research, cooperation with the States and private
forest owners, and management of the National
Forests and National Grasslands, it strives —
as directed by Congress — to provide increasingly
greater service to a growing Nation.