Dalmatian
toadflax (Linaria dalmatica)
From
the Nature Conservancy, Wildland Invasive Species Team
Send questions or comments about this page to Alan Carpenter &
Thomas Murray, Land Stewardship Consulting, 2941 20th Street, Boulder,
CO 80304
Linaria
genistifolia ssp. dalmatica and Linaria vulgaris are perennial herbs
of the figwort family (Scrophulariaceae). Both species are classified
as weeds in Europe, Russia, Canada, and the United States, and are
common throughout North America. The name "toadflax" will
be used when referring to both species in this ESA.
A toadflax
plant contains from 1-25 vertical, floral stems. These floral stems
have thick- walled, woody xylem and supporting fibers. Flowers are
bright yellow and resemble snapdragons. The tap root may penetrate
one meter into the soil. Horizontal roots may grow to be several
meters long, and can develop adventitious buds that may form independent
plants.
Linaria
genistifolia ssp. dalmatica
Linaria
genistifolia ssp. dalmatica is most common in the western United
States and has a tolerance to low temperatures and coarse soils.
The worst-infested states are California, Idaho, Montana, Oregon,
Washington, and Wyoming. Dalmatian toadflax is listed as a noxious
weed in Colorado, Arizona, and New Mexico.
Mature
dalmatian toadflax plants grow to be between 0.8 to 1.5 m tall.
Leaves are broad, 2-5 cm long, ovate to ovate-lanceolate, 1-2.5
cm long and are alternate, generally clasping but crowded.
Flowers
are born in loose, elongate, terminal racemes. The pedicels are
2-4 mm long when the flowers are mature and releasing pollen. The
calyx is 5-7.5 mm long, the segments subequal, broadly lanceolate
to ovate, sharply acute, and rigid. The corolla is strongly two-lipped
and 14-24 mm long, excluding the 9-17 mm spur. The upper lip is
10-15 mm long. The lower lip is 5-11 mm long with a well-developed
palate closing off the throat. The palate is densely white to orange
bearded. Flowers are bright yellow. Linaria genistifolia ssp. dalmatica
typically flowers from May to August.
Linaria
genistifolia ssp. dalmatica produces egg-shaped to nearly round
capsulate fruits 4-10 mm long by 4-8 mm wide. Seeds are sharply
angular, slightly winged, and 1-2 mm long. A mature plant can produce
up to 500,000 seeds annually, and they can remain dormant for up
to ten years. Dalmatian toadflax produces seed from July to October.
Linaria
vulgaris
Linaria
vulgaris is common in eastern North America but can be found in
many areas of the west. The worst-infested western states are Idaho,
Montana, Oregon, and Washington. Linaria vulgaris is listed as a
noxious weed in Arizona and New Mexico.
Yellow
toadflax is smaller than dalmatian toadflax and grows to be 0.2
to 0.8 meters tall. Yellow toadflax leaves are soft, linear or linear
lanceolate, sessile, and pale green. They are generally 2.5 cm long
by 2-4 mm wide (Morishita 1991).
The
flowers of Linaria vulgaris are similar to those of Linaria genistifolia
ssp. dalmatica. Yellow toadflax flowers from May to August.
Yellow
toadflax seeds are flattened, winged and 1-2 mm long. A mature plant
can produce up to 30,000 seeds annually. A single stem has been
reported to contain over 5,000 seeds (Saner et al. 1995). Linaria
vulgaris produces seed from July to October.
Stewardship
Summary
Both
Linaria genistifolia ssp. dalmatica and Linaria vulgaris rapidly
colonize open sites. They are most commonly found along roadsides,
fences, range lands, croplands, clear cuts, and pastures. Disturbed
or cultivated ground is a prime candidate for colonization. Toadflax
can significantly reduce crop yields and stress native communities.
In one study, toadflax-free plots produced 2.5 times more grass
than plots where toadflax was present (Robocker 1974). In Alberta,
yellow toadflax densities of over 180 stems/m2 reduced the seed
yields of some forage crops by 33% (Saner et al. 1995).
The seedlings of toadflax are considered ineffective competitors
for soil moisture with established perennials and winter annuals
(Morishita 1991). However, once established both species of toadflax
suppress other vegetation mainly by intense competition for limited
soil water. Mature plants are particularly competitive with winter
annuals and shallow-rooted perennials (Robocker 1974).
Successful
control can be obtained by pulling, or killing the plants with herbicide,
before toadflax seed production begins. Since the plant also spreads
through vegetative propagation, and the seeds can remain dormant
for up to ten years, this process must be repeated every year for
at least ten years to completely remove a stand. Competitive perennial
grasses and forbs should be planted to utilize water and nutrients
that would otherwise be readily available to toadflax.
Impacts
(Threats Posed by this Species)
Both
species are persistent, aggressive invaders and capable of forming
colonies through adventitious buds from creeping root systems. These
colonies can push out native grasses and other perennials, thereby
altering the species composition of natural communities. In North
America, both species of toadflax are considered strong competitors.
They are quick to colonize open sites, and are capable of adapting
growth to a wide range of environmental conditions (4). Linaria
genistifolia ssp. dalmatica and Linaria vulgaris are listed as weeds
in North America, and are on noxious weed lists of several states
and Canadian provinces.
Low-till cultivation practices have contributed to the resurgence
of toadflax populations on agricultural lands (McClay 1992). By
not tilling the soil, and subsequently damaging the root system
of toadflax plants, toadflax colonies have been able to flourish.
Intensive clean cultivation techniques are recommended for successful
toadflax control on agricultural land. This requires at least two
years with 8-10 cultivations in the first year and 4-5 cultivations
in the second year (Morishita 1991).
Global
Range
Linaria
genistifolia ssp. dalmatica
Dalmatian
toadflax is a native of the Mediterranean region from the coast
of Croatia northeastward to Transylvania and Moldavia in northern
Romania, southward and eastward around the Black Sea in the countries
of Bulgaria, Albania, Greece, Crete, Turkey, Syria, Iran, and Iraq
(Alex 1962). It generally grows in open, sunny places, from sea
level up to 2,800 meters (roughly 9,200 feet). Linaria genistifolia
ssp. dalmatica was first reported in North America in 1894 by T.
D. Hatfield. He was a gardener in Massachusetts who was growing
it as a perennial herbaceous ornamental (Alex 1962).
Linaria
vulgaris
Yellow
toadflax is a native of southeastern Europe and southwestern Asia.
The present world distribution includes most of Europe and Asia,
and it has been introduced to Japan, Australia, New Zealand, South
Africa, Jamaica, Chile and North America. In North America, yellow
toadflax is found throughout the continental United States and in
every Canadian province and territory (Saner et al. 1995).
Linaria
vulgaris is recorded as first being introduced to America from Wales
as a garden ornamental by a Welsh Quaker who came to Delaware with
William Penn. It flourished and was cultivated at other colonial
gardens where it spread into the wild (Mitich 1993).
Habitat
In
North America, Linaria genistifolia ssp. dalmatica and Linaria vulgaris
primarily occur on sandy or gravely soil on roadsides, railroads,
pastures, cultivated fields, range lands, and clear cuts (Saner
et al. 1995). Both species of toadflax can adapt their growth to
fit a range of habitats, and have a tolerance for low temperatures
and coarse textured soils. They have a northern limit of 55º
to 65º latitude.
Linaria
genistifolia ssp. dalmatica is most common in the western United
States while Linaria vulgaris is common throughout eastern North
America, but is also found in areas of the west. In northeastern
Washington, Linaria genistifolia ssp. dalmatica is spread throughout
open, low-elevation, coniferous forests and adjacent shrub-steppe.
In the province of Alberta, a 1987 survey estimated an infestation
of Linaria vulgaris of 28,000 hectares (Saner et al. 1995). In Colorado,
Linaria genistifolia ssp. dalmatica is commonly found between 1,524
to 1,981 meters (5,000 to 6,500 feet) in oak, aspen, sagebrush,
mountain brush, and riparian communities. Linaria vulgaris is typically
found from 1,829 to 2,591 meters (6,000 to 8,500 feet) on the western
slope, but can also be found on the eastern slope of the state (4).
In New England, Linaria vulgaris is occasionally a serious weed
problem that leads to the premature abandonment of fields (Saner
et al. 1995).
Biology-Ecology
Both
Linaria genistifolia ssp. dalmatica and Linaria vulgaris are considered
strong competitors in North America. Both species reproduce by seed
and vegetative propagation. Once established, high seed production
and the ability for vegetative reproduction allow for rapid spread
and high persistence (Saner et al. 1995).
Both
Linaria genistifolia ssp. dalmatica and Linaria vulgaris are self-incompatible,
and rely upon insects for pollination. The two most important pollinators
are bumble bees and halictid bees (Zimmerman 1996). Spring emergence
occurs about mid-April and depends primarily on temperature. The
stems of seedling plants seldom exceed 40 cm. First leaves are 1
cm long. Prostrate stems emerge in September and produce leaves
that are ovate, 3.8 cm by 2.2 cm in size. Prostrate stems are tolerant
to freezing and are associated with floral stem production the following
year (Robocker 1974).
The
strong upright floral stems that characterize mature toadflax plants
develop after a winter’s dormancy, and emerge about the same
time as new seedlings in mid-April. A single plant will produce
from 1-25 floral stems. The ultimate survival of the stand, and
probability of re-establishment, depends heavily on the number of
floral stems and their seed production (Robocker 1974). Flowering
occurs from May-August and seeds mature from July-September. A mature
dalmatian toadflax can produce up to 500,000 seeds annually (Morishita
1991). A large yellow toadflax can produce up to 30,000 seeds annually
(Saner et al. 1995).
Both
species can reproduce vegetatively. Stems develop from adventitious
buds on primary and lateral roots. Vegetative reproduction from
root buds can occur as early as 2-3 weeks after germination, and
is possible from root fragments as short as 1 cm in length (Zimmerman
1996). These buds can grow their own root and shoot systems, and
become independent plants the next year. Vegetative propagation
can allow a stand of toadflax to spread rapidly. In one study, a
stand of L. vulgaris increased by 418% in a single season, and a
patch that was originally one acre in size expanded to cover 85
acres in a five-year period (Zimmerman 1996).
In
addition to promoting growth, the large, deep, root systems of Linaria
genistifolia ssp. dalmatica and Linaria vulgaris exploit water efficiently.
The tap root may penetrate 1 meter into the soil and lateral roots
may be several meters long. The deep root system prevents grazing
and shallow cultivation methods from dislodging or destroying plants
(Saner et al. 1995).
Yellow
toadflax contains a poisonous glucoside that is reported to be mildly
poisonous to livestock (Morishita 1991). However, both species are
considered unpalatable and reports of livestock poisonings are rare.
Linaria
genistifolia ssp. dalmatica and Linaria vulgaris have relatively
short lifespans. Individual plants live up to five years with an
average lifespan of 3.8 years (Robocker 1974). The life span of
toadflax stands is dependent on environmental conditions and the
reproductive success of individual plants. The relatively short
lifespan of toadflax plants bodes well for controlling these species.
Recovery
Potential
The
recovery potential of areas that have been cleared of toadflax is
very high. The Magnusson Butte Preserve in Washington experienced
increases in native and non-native annual grasses, forbs, and residual
native perennial forbs following the removal of toadflax stands
(Cornelius 1995). Communities that are in good condition may recover
without replanting of desirable species as long as follow-up control
visits are conducted annually. However, replanting competitive native
grasses and forbs can help accelerate recovery of the area.
Monitoring
Requirements and Procedures
Monitoring
should be conducted in early June when toadflax plants have formed
buds and are beginning to flower. Any management program should
also be conducted during the month of June. This is when root carbohydrate
reserves are at their lowest, which makes it more difficult for
the root system to recover. Follow-up work in late June or early
July is recommended to locate and remove any late-flowering plants.
Management
Programs
The
key to managing Linaria genistifolia ssp. dalmatica and Linaria
vulgaris is to: 1) eliminate or greatly reduce seed production from
established individuals (by cutting or pulling seed stalks prior
to seed set, or by using insects to destroy flowers, seeds, or damage
plants sufficiently so that no or few seeds are produced); and 2)
destroy toadflax seedlings that arise from the soil seed bank before
these plants become established (as above, plus herbicide).
Several
insect species have been introduced as biological control agents
for both toadflax species but none of them completely eliminate
infestations. Also, the diverse geographic range of toadflax throughout
North America makes it unlikely any one species of insect will be
effective everywhere. Herbicide treatment, if applied at the right
time, can significantly reduce toadflax seed production. Cutting,
mowing, and discing of toadflax plants can be effective on agricultural
lands if repeated annually.
A decade-long
hand pulling experiment at the Magnusson Butte Preserve, in Washington,
demonstrated how effective pulling could be. The experiment was
first conducted in a 5 by 5 meter test plot, but was soon expanded
over the whole 28 acre preserve. During the first week of June,
a team of about 30 volunteers walked the preserve pulling all toadflax
plants they found. The first week of June was an ideal time as the
flowers were just beginning to appear, making the plants easier
to locate. Also, the soil was still damp, which allowed for easy
pulling without significant soil disturbance. At first, the stems
were removed in bags to avoid a mulching effect on desirable native
plants, but in later years when there were fewer plants they were
simply dropped in place with no ill effect. A follow-up visit was
conducted during the last week in June to remove any late-flowering
plants that might have been missed. Teams were able to reduce the
number of flowering stems each year by an estimated 90-95% preserve-wide.
In the third year, it was noticed that flowering stems were not
only reduced in number, but were significantly smaller in size and
lower in vigor. The test plot also experienced an increase in native
and non-native grasses and perennial forbs (Cornelius 1995).
This
experiment in non-chemical control had some unforeseen benefits.
The pulling program turned into a great community outreach program
in that area. It allowed for new volunteers to become familiar with,
and take an interest in, the Magnusson Butte Preserve.
Biological
Control
Five
insects species have been approved by the USDA-APHIS-PPQ for release
as biological control agents for Linaria genistifolia ssp. dalmatica
and Linaria vulgaris. Anecdotal evidence to date suggests these
insects have not been highly effective in controlling toadflax.
A permit must be obtained from the USDA, Animal and Plant Health
Inspection Service (APHIS) before you can transport these agents
between states. Information on how to obtain a permit can be found
at the bottom of this section under Obtaining permits for field
releases. Additionally, authorities that can be contacted for more
information about each species are listed at the end of each section.
Brachypterolus
pulicarius
Brachypterolus
pulicarius is a shoot and flower-feeding beetle that was accidentally
introduced from Europe. B. pulicarius is considered a biological
agent for both Linaria vulgaris and Linaria genistifolia ssp. dalmatica.
Adults emerge in May and feed on young toadflax stems and shoot
tips. They mate in early June and the females lay eggs in the flower
buds. The young larvae feed primarily on the anthers and ovaries
in the buds and flowers, and the older larvae feed on maturing seeds
(Harris 1961). An experiment using B. pulicarius indicated the beetle
has no effect on root or shoot biomass of attacked plants. However,
it delayed the onset of flowering of Linaria vulgaris for 27 days.
The most significant effect was that total seed production was reduced
by 74% on attacked plants (McClay 1992). B. pulicarius is currently
found in most toadflax stands in Alberta and southern Saskatchewan.
It contributed to a decline in the spread of Linaria vulgaris in
Canada in the 1960’s (McClay 1992).
Authorities
for B. pulicarius
Eric
M. Coombs, Oregon Department of Agriculture, 635 Capitol St. NE,
Salem, OR 97310
Robert
M. Nowierski, Department of Entomology, 413 Leon Johnson Hall, Montana
State University, Bozeman, MT 59717
Gary
L. Piper, Department of Entomology, Washington State University,
Pullman, WA 99164-6382
Calophasia
lunula
Calophasia
lunula is a defoliating moth that is native of Eurasia and was introduced
into the United States in 1968 to control both species of toadflax.
In Canada, the moth defoliated up to 20% of the toadflax stems where
it was established. Multiple releases of C. lunula were made in
Colorado, Arizona, Montana, Oregon, Washington, and Wyoming, but
no establishment of the moth was recorded on either toadflax species
until 1989 (McDermott 1990). In 1989, C. lunula larvae were found
on dalmatian toadflax plants just outside of Missoula, Montana.
Since 1989, C. lunula has been established in three other sites
in Montana, two sites in Idaho, and has become widely distributed
throughout northeastern Washington (Rees et al. 1996). Studies show
C. lunula is adversely affected by cold-temperatures, and this might
be linked to its failure to establish in other states, and at higher
altitudes (McClay and Hughes 1995). However, recent establishment
success has renewed hopes that Calophasia lunula may become a significant
biological control of toadflax in the United States.
Authorities
for C. lunula
Robert
M. Nowierski, Department of Entomology, 413 Leon Johnson Hall, Montana
State University, Bozeman, MT 59717
Gary
L. Piper, Department of Entomology, Washington State University,
Pullman, WA 99164-6382
Jim
S. Story, Western Agricultural Research Center, 580 NE Quest Lane,
Corvallis, MT 59828
Eteobalea
serratella and Eteobalea intermediella
E.
serratella and E. intermediella are small root-boring moths native
to the Mediterranean region and central Europe. Eggs are deposited
in the leaf axils, or at the base of the stem. Larval mining occurs
in the root crown area and causes substantial damage to the root
system (Rees et al. 1996). Attacked plants had a shorter flowering
season and produced seeds of lower weight. However, reduced seed
weight of Linaria vulgaris has not been correlated with lower germination
rates and root mining had no effect on plant survival (Saner and
Muller-Scharer 1994). Continued root mining in the winter resulted
in a doubling of stem production the following spring, but the total
plant biomass remained the same (Saner and Muller-Scharer 1994).
Authority
for E. serratella and E. intermediella
Robert
M. Nowierski, Department of Entomology, 413 Leon Johnson Hall, Montana
State University, Bozeman, MT 59717
Gymnaetron antirrhini
Gymnaetron
antirrhini is a seed-eating weevil native to Eurasia. It was accidentally
introduced into the United States and is now established in Idaho,
Montana, Oregon, Washington, and Wyoming. G. antirrhini attacks
yellow toadflax and one strain has adapted to dalmatian toadflax
(Rees et al. 1996). Adults emerge in May to feed on young toadflax
stems. They mate in June and the females lay eggs in the ovaries
of the flowers. The larvae feed on immature seeds in the seed capsules.
The mature larvae construct oval cells within the seed capsules
where pupation occurs. G. antirrhini can reduce seed production
in yellow toadflax by 85-90% (Rees et al. 1996).
Authorities
for G. antirrhini
Eric
M. Coombs, Oregon Department of Agriculture, 635 Capitol St. NE,
Salem, OR 97310
Robert
M. Nowierski, Department of Entomology, 413 Leon Johnson Hall, Montana
State University, Bozeman, MT 59717
Gary
L. Piper, Department of Entomology, Washington State University,
Pullman, WA 99164-6382
Obtaining
permits for field releases
To
introduce one of the biological control agents described above into
your state, you must first obtain a permit from the USDA-APHIS-PPQ.
To obtain a permit you must complete a form PPQ-526, "Application
and Permit to Move Live Plant Pests or Noxious Weeds", and
send the application to the Department of Agriculture in the state
where the release is to be made. The form must be signed and sent
for processing to the USDA-APHIS-PPQ office, Biological Assessment
and Taxonomic Support (BATS), 4700 River Road, Unit 113, Riverdale,
MD 20737. When this is signed by PPQ, a copy will be returned to
the applicant as an approval record.
To
find the phone number and address of the APHIS-PPQ State Plant Health
Office in your state check on-line at: (http://www.aphis.usda.gov/oa/ppqoffice.html).
For more information about the permit process, to download forms,
check the status of your permit, or to search the Code of Federal
Regulations, you can browse the APHIS-PPQ home page at: (http://www.aphis.usda.gov/ppq/bats/permits/).
Finally, an expedite list of all insects, mites, and nematodes that
require APHIS permits can be found on-line at: (http://www.aphis.usda.gov/ppq/bats/weedagen.htm).
TNC
policy as of Spring 1998 requires that you receive prior authorization
from the Home Office Director of Conservation Science for intentional
release of any non-native biological control agents on a TNC preserve
(see TNC Policies and Procedures manuals for details).
Burning
Burning
is not a recommended control method for Linaria genistifolia ssp.
dalmatica and Linaria vulgaris (Saner et al. 1995). The large, deep,
root systems of both species protect them from burning. In fact,
areas that have been recently disturbed by fire are susceptible
to increased toadflax infestation.
Chemical
Permanent,
long-term control cannot be achieved with herbicide treatment alone
(Saner et al. 1995). Herbicides should be applied during flowering
when carbohydrate reserves in the root of the plants are at their
lowest. At the latest, herbicide treatment should be applied before
seed dispersal, if it is to be effective.
The
herbicides glyphosate, dicamba and picloram are considered effective
for controlling toadflax. A six-year study found that phenoxypropionic
herbicides such as diclorprop were more effective at controlling
toadflax than phenoxyacetic herbicides such as 2,4-D (Robocker 1968).
2,4-D, MCPA, MCPB, and mecoprop do not control toadflax.
Picloram
Trade
name(s): Tordon
Picloram
applied at the rate of 2.25 kg/ha was considered an effective control
of toadflax during a two-year test (Morishita 1991). Bending and
twisting of leaves and stems is evident almost immediately after
application.
Picloram
is an auxin-type herbicide that causes disorganized plant growth
when applied. Auxin-type herbicides are used for control of annual,
perennial, and creeping perennial broad-leaved plants. All auxin-type
herbicides are organic acids which take on a negative charge after
ionization of acids and salts (Ross and Childs 1998). Picloram does
not bind to soil and may leach to groundwater. Its average half-life
in soil is 90 days, with a range of 20 - 330 days (Ahrens 1994).
Its half-life in water is 2.3 - 41.3 days (6). Dissipation is relatively
slow under the cool, dry conditions prevalent in much of the northwestern
U. S. Picloram is not expected to bio-concentrate in aquatic organisms.
In
humans, the EPA found that acute exposures to picloram could cause
weakness, diarrhea, weight loss, and central nervous system damage.
Long-term exposure above safe drinking water levels has the potential
to cause liver damage (6).
Although picloram is effective at managing toadflax, it is a relatively
non-selective compound, and has been observed to have a residual
effect on other perennial broad-leaved plants. Damage to non-target
vegetation is a major problem associated with all auxin-type herbicides
(Ross and Childs 1998).
Dicamba
Trade
name(s): Banvel, Clarity, Vanquish, Veteran
Dicamba
applied at concentrations of 2.25 kg/ha was considered effective
at controlling toadflax (Morishita 1991). Dicamba controls annual
and perennial broad-leaved weeds in grain crops, grasslands, pastures,
and range land.
Like
picloram, dicamba is also an auxin-type herbicide, and has the same
side effects. It is a relatively non-selective compound and can
have a residual effect on non-target broad-leaved plants.
Dicamba
does not bind to soil and may leach into groundwater. Its half-life
in soil can vary from 4-555 days (2). Its potential to persist for
long periods limits its use in natural areas. In water, dicamba
does not bio-concentrate in organisms, and is broken down mainly
by microbial degradation. When used according to instructions, dicamba
poses little threat to wildlife (2). Dicamba is considered only
slightly toxic to birds, and is of low toxicity to fish and aquatic
organisms. Dicamba is not toxic to bees.
In
humans, acute exposure to dicamba is moderately toxic by ingestion
and slightly toxic by inhalation or dermal exposure. Symptoms of
poisoning with dicamba include loss of appetite, vomiting, muscle
weakness, slowed heart rate, shortness of breath, central nervous
system effects, and exhaustion following repeated muscle spasms
(2).
Glyphosate
Trade
name(s): Roundup, Rodeo, Accord
Glyphosate
has been used in Canada to control toadflax in crops, and is also
recommended for spot treatments. Glyphosate applied at early bloom
at 1, 2, and 4 kg per hectare provided 40, 70, and 90% control that
season (Saner et al. 1995). However, abundant regrowth from the
root systems occurred the following year.
Glyphosate
inhibits production of the aromatic acids tryptophan, tyrosine and
phenylalanine which are all needed for protein synthesis and other
biosynthetic pathways. It is a relatively non-selective compound
used to control broad-leaved weeds and grasses. Glyphosate will
kill or damage non-target plants but this can be minimized by applying
it directly to the leaves of toadflax or other targeted plants.
Uses are limited to foliar applications since it is rapidly inactivated
in the soil (Ross and Childs 1998).
Glyphosate
biodegrades in soil and has a half-life of 47 days, according to
Ahrens (1994). It has been stated that because glyphosate strongly
adsorbs to clay particles, crops can be planted immediately after
it has been applied. Greenhouse studies by Ahearn-Myerson et al.
(1997), however, showed glyphosate may persist in an active form
in soils for as long as 79 days. This contrasts with technical information
on glyphosate which indicates it degrades rapidly due to normal
soil microbial activity, and that it is not active once it contacts
the soil or muddy water because it complexes with clay particles.
Ahearn-Myerson et al have not yet duplicated their study in the
field but based on their greenhouse studies, they recommend that
restorationists and others who use glyphosate should not re-plant
treated areas until several weeks past the interval suggested by
the manufacturer. Glyphosate’s half-life in water is a few
days, and it is not expected to bio-concentrate in aquatic organisms
(5).
In
humans, acute exposure to glyphosate can cause lung congestion and
an increased breathing rate. Long-term exposure to glyphosate above
safe levels has the potential to cause kidney damage, and effects
on the reproductive system (5).
Additional
information on herbicides
More
information on chemical control of toadflax can be obtained from
the Weed Management Library at 1-800 554-WEED, or from your State
Weed Specialist.
Arizona:
Everett Hall, Arizona Department of Agriculture, (602) 542-3309
California:
Nate Dechoretz or Ross O’Connell, California Department of
Agriculture Integrative Pest Management, (916) 654-0768
Colorado:
Dr. George Beck, Colorado State University, (970) 491-7568
Idaho:
Dr. Bob Callahan, University of Idaho, (208) 885-6617
Montana:
Roger Sheley, Montana Department of Agriculture Extension Services,
(406) 994-5686
New
Mexico: Dr. Richard Lee, New Mexico State University, (505) 646-2888
Oregon:
Tim Butler, Oregon Department of Agriculture Noxious Weed Control
Program, (503) 986-4625
Utah:
Dr. Steve Dewey, Utah State University, (801) 750-2256
Washington:
Greg Haubrich, Washington Department of Agriculture, (509) 576-3039
Wyoming:
Dr. Tom Whitson, University of Wyoming, (307) 766-3113
Cutting,
Mowing and Discing
Cutting
or removal of the above ground portion of toadflax plants reduces
the current year growth, but it will not kill them. Cutting toadflax
stands in spring or early summer is an effective way to eliminate
plant reproduction through seed production and dispersal. However,
the long dormancy of toadflax seeds requires that the process be
repeated annually for up to ten years.
Mowing
might be even less effective on toadflax compared to cutting since
it cuts the plants several cm above the soil surface which may allow
them to resprout more rapidly. For example bull thistle plants (Cirsium
vulgare) cut at the soil surface did not recover but a high percentage
of plants cut 5-10 cm above the soil surface resprouted (Randall
pers. comm.). In addition, damage to surrounding plants and species
should be evaluated before mowing is used.
Discing
can be an effective method of toadflax control on agricultural lands.
Successful control can be obtained by using intensive clean cultivation.
This method requires at least two years with eight to ten cultivations
in the first year, and four to five cultivations the second year
(Morishita 1991).
Grazing
Grazing
does not control either species of toadflax. Toadflax is considered
unpalatable, and yellow toadflax contains a glucoside that is mildly
poisonous to livestock. Additionally, ground disturbance created
by intensive grazing actually creates ideal habitat for toadflax
infestation. Effective grazing management is necessary to reduce
toadflax in pastures and range lands.
Manipulation
of Water Level and Salinity
No
studies were found indicating that manipulating water levels or
soil salinity to control toadflax have been tested.
Pulling
Hand
pulling toadflax before seed set each year can be an effective control
method. The hand pulling experiment on the Magnusson Butte Preserve
in Washington showed that toadflax can be significantly reduced
by pulling once a year as long as new seed is eliminated. Once again,
this method must be repeated annually for up to ten years to completely
remove a stand.
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