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Important
Note:
Pesticide registrations change frequently. As of 2004,
Acephate is no longer registered while Dimilin is registered by EPA
for rangeland grasshopper control.
VII.10
Ongoing Environmental Concerns
L. C. McEwen
Indirect Effects
on T and E Species
New Chemicals and
Biologicals
Species of Concern
Function
of Wildlife in a GHIPM System
References
Perhaps the greatest continuing environmental concern in a Grasshopper
Integrated Pest Management (GHIPM) program is providing safeguards
and protection for threatened and endangered (T and E) plant and
animal species. These problems complicate grasshopper control programs
and make them more costly but must be dealt with in a straightforward
manner. Plenty of lead time should be allowed to identify species
and habitats and to work out solutions with agencies responsible
for T and E species' protection and management.
Recognition of the fact that individual vertebrate animals can
vary greatly in their sensitivity to a given toxic chemical should
help all workers understand that toxic exposure of the T and E species
must be kept to a minimum. Toxic hazard is minor for mature animals
lightly exposed to the current GHIPM pesticides-carbaryl, malathion,
and acephate-but is probably more of a factor for young animals
(chicks, nestlings, amphibians, and larval fish). Any toxic mortality
would be of concern because species differ in their lower threshold
of numbers of animals necessary for maintaining a viable population.
Those limits are not known precisely for each species, but land
managers should try hard not to cause unnecessary losses with toxic
chemicals.
In the larger picture, it would seem that concern for geographic
variants that have been given T and E status should not be on the
same level as for T and E species that are the sole remaining population
or individuals. Technically and legally, however, there is no distinction
at this time.
T and E species can be protected in several ways in a rangeland
grasshopper cooperative control program. Nonspray buffer zones are
one of the main tools (see chapter III.8).
Width and size of buffer zones will vary with the T and E species
and on the outcome of consultation with managing agencies. Carbaryl
bait treatments or other dry baits, including biological control
agents such as Nosema locustae and Beauveria bassiana,
can be used safely much closer to the T and E species habitat
or even with no buffer zone in some cases.
Baits and biologicals add expense and sometimes cause equipment
problems when used but should be recognized and accepted as important
and necessary components of many successful programs. The degree
of grasshopper reduction will probably be less than where liquid
insecticide spray is applied, but the higher densities of grasshoppers
remaining after the treatment often will be beneficial to the T
and E species.
Another possible option for protecting T and E species is the timing
of the grasshopper control program. This aspect can be explored
for T and E insects and pollinators of T and E plants (also see chapter III.5).
If the T and E insects are in the adult stage for a relatively brief
period, then pest managers may conduct treatments safely before
or after the adult stage.
For aquatic species, there are significant differences in toxicity
among the three chemicals. Acephate is much less toxic to fish than
carbaryl or malathion (Johnson and Finley 1980) and is referred
to in other publications as practically nontoxic to fish. Acephate
is highly effective against grasshoppers at the low application
rate of 1.5 oz/ acre (0.105 kg/ha) (U.S. Department of Agriculture
1987). Although acephate has been little used in cooperative control
programs, it could be an excellent alternative to other pesticides
where T and E fish are of concern. Another safety factor for fish
would be to use dry bait treatments because less chemical is used
per unit area and there is much less potential for drift into aquatic
habitat. The entire problem of T and E species protection in GHIPM
programs could benefit from further research.
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Indirect
Effects on T and E Species
The question of indirect effects of grasshopper control programs,
primarily reduction or loss of the food base for birds, now comes
up more frequently than potential toxic effects. Colorado State
University (CSU)-led studies have shown that when grasshopper availability
is reduced, birds generally switch to other insects or invertebrates
for food and maintain their nesting success and populations (Miller
1993, Miller and McEwen 1995, Miller et al. 1994, George et al.
1995, Fair et al. 1995). Regarding the concern for peregrine prey
effects, CSU investigators have shown that total bird population
numbers do not decline following a grasshopper control program,
even though some individual species might decrease (George et al.
1995). Since peregrines prey on such a wide variety of avian species
(DeWeese et al.1986, Hunter et al. 1988), the decline of one or
two species should have no significant effect on their prey base.
Use of dry baits, such as carbaryl bait, also could be a safeguard
since the baits are selective formulations and consequently leave
many unaffected insects for avian food (Adams et al. 1994).
Nevertheless, each T and E species must be examined individually
for potential response to GHIPM treatments. The situation is such
that T and E species and their habitats cannot be dealt with routinely
by generalized procedures. Each T and E situation must be treated
as a unique case history, although as knowledge is acquired, some
will be more standardized than others.
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New
Chemicals and Biologicals
New materials for range grasshopper control, such as Dimilin®
(diflubenzuron) and Beauveria bassiana, will require close
monitoring until their environmental safety is determined. The two
materials appear quite safe for terrestrial vertebrates, but final
determinations cannot be made until the materials are applied in
large-scale operational control programs. Aquatic effects are especially
of concern as well as Acridid (grasshopper) specificity and effects
on nontarget invertebrates. Any other candidate chemicals and biologicals
that are considered for GHIPM must also be closely examined for
environmental effects before being approved for large-scale use.
Species
of Concern
State and Federal wildlife agencies in recent years have endorsed
a philosophy of giving attention to declining species before
they reach T and E status. If a declining species can be managed
for recovery before listing, management efforts are simplified.
Declining species may be designated as species of concern. Some
examples are the long-billed curlew (Numenius americanus), the
western burrowing owl (Athene cunicularia), and the ferruginous
hawk (Buteo regalis). The curlews and burrowing owls use
grasshoppers heavily, especially as a source of protein and nutrients
important for breeding and for feeding their young. The golden eagle
(Aquila chrysaetos) is another species of concern in some
areas of the West and is a protected species. There is a need to
conduct a study of the response of nesting golden eagles to malathion
spray as was done with Sevin® 4-Oil. One or more of several
species of concern are apt to be present in GHIPM treatment areas
and should be treated as T and E species if necessary in the opinion
of the biologists and land managers involved.
Gallinaceous birds, such as prairie chickens and sharptailed grouse
(Tympanuchus spp.), sage grouse (Centrocercus urophasianus),
chukars (Alectoris chukar), and wild turkeys (Meleagris
gallopavo), also often are considered species of concern. The
effects of grasshopper control on the growth and survival of the
young chicks and poults is the primary question. More study is needed
on the effects of GHIPM programs on species of concern.
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Function
of Wildlife in a GHIPM System
Scientists and land managers have made a lot of progress in showing
the role and benefits of wildlife, especially birds, as important
contributors to regulation of grasshopper densities (Joern 1986,
Fowler et al. 1991, Bock et al. 1992). However, the overall ecology
of native wild vertebrates in preventing insect pest outbreaks is
virtually unexplored. The interrelationships of range condition,
vegetative cover types, native plants vs. introduced species
for reseeding (such as crested wheatgrass, Agropyron cristatum),
and associated wildlife populations need much more investigation.
Large expanses of crested wheatgrass become devoid of almost all
the breeding avian species (Reynolds and Trost 1980). In the northern
Great Plains, grasshopper outbreaks frequently originate in crested
wheatgrass, where grasshopper densities are usually higher than
on native grass range (Hirsch et al. 1988 unpubl., Kemp and Onsager
1994 unpubl.). This fact should not be surprising because the lack
of birds as grasshopper predators is coupled with >40 percent
bare ground (compared to <5 percent in native grassland (Dormaar
et al. 1995), which is favored by many grasshoppers for egg-laying.
Range condition criteria are currently undergoing review and revision
(Task Group on Unity in Concepts and Terminology 1995). Land managers
need to relate range wildlife habitat use and populations to condition
classes and to grasshopper population fluctuations. Improving range
condition is a long, slow process, but range in good.VII.10-3 condition
with a full complement of native wildlife can reduce grasshopper
population fluctuations in the central and northern Great Plains
(McEwen 1987). Improving the condition of degenerated sagebrush
(Artemisia spp.) range found farther west is more difficult
than improving other range types, but it should be a long-term goal
(McEwen and DeWeese 1987). New range management practices (Biondini
and Manske 1996; Onsager, in press) should be examined for wildlife
responses.
The status and function of wild vertebrates in relation to range
condition also need more investigation. Basic knowledge of range
wildlife ecology connects with the efforts to improve the vegetative
cover on western rangelands. Preventing the extinction of animal
and plant species is the goal of conservation biology and will be
a benefit of better range condition. This will also be an important
factor contributing to grasshopper management in an IPM system.
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References
Cited
Adams, J. S.; Knight, R. L.; McEwen, L. C.; George,
T. L. 1994. Survival and growth of nestling vesper sparrows exposed
to experimental food reductions. The Condor 96: 739-748.
Biondini, M. E.; Manske, L. L. 1996. Grazing frequency
and ecosystem processes in a northern mixed prairie. Ecological
Applications 6: 239-256.
Bock, C. E.; Bock, J. H.; Grant, M. C. 1992. Effects
of bird predation on grasshopper densities in an Arizona grassland.
Ecology 73: 1706-1717.
DeWeese, L. R.; McEwen, L. C.; Hensler, G. L.;
Petersen, B. E. 1986. Organochlorine contaminants in Passeriformes
and other avian prey of the peregrine falcon in the Western United
States. Environmental Toxicology and Chemistry 5: 675-693.
Dormaar, J. H.; Naeth, M. A.; Williams, W. D.;
Chanasyk, D. S. 1995. Effect of native prairie, crested wheatgrass
(Agropyron cristatum) (L.)(Gaertn.) and Russian wildrye (Elymus
junceus Fisch.) on soil chemical properties. Journal of Range
Management 48: 258-263.
Fair, J. M.; Kennedy, P. L.; McEwen, L. C. 1995.
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Fowler, A. C.; Knight, R. L.; George, T. L.; McEwen,
L. C. 1991. Effects of avian predation on grasshopper populations
in North Dakota grasslands. Ecology 72(5): 1775-1781.
George, T. L.; McEwen, L. C.; Petersen, B. E. 1995.
Effects of grasshopper control programs on bird populations in western
rangelands. Journal of Range Management 48: 336-342.
Hunter, R. E.; Crawford, J. A.; Ambrose, R. E.
1988. Prey selection by peregrine falcons during the nestling stage.
Journal of Wildlife Management 52: 730-736.
Joern, A. 1986. Experimental study of avian predation
on coexisting grasshopper populations (Orthoptera: acrididae) in
a sandhills grassland. Oikos 46: 243-249.
Johnson, W. W.; Finley, M. T. 1980. Handbook of
acute toxicity of chemicals to fish and aquatic invertebrates. Publ.
137. Washington, DC: U.S. Department of the Interior, U.S. Fish
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McEwen, L. C. 1987. Function of insectivorous birds
in a shortgrass IPM system. In: Capinera, J. L., ed. Integrated
pest management on rangeland: A shortgrass prairie perspective.
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McEwen, L. C.; DeWeese, L. R. 1987. Wildlife and
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Miller, C. K. 1993. Responses of nesting savannah
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M.S. thesis. Ft. Collins, CO: Colorado State University. 24 p.
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Responses of nesting savannah sparrows to fluctuations in grasshopper
densities in interior Alaska. Auk 111: 960-967.
Miller, C. K.; McEwen, L. C. 1995. Diet of nesting
savannah sparrows in interior Alaska. Journal of Field Ornithology
66: 152-158.
Onsager, J. A. [In press.] Suppression of grasshoppers
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Reynolds, T. D.; Trost, C. H. 1980. The response
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of Range Management 48: 271-282.
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References
Cited-Unpublished
Hirsch, D. C.; Reuter, K. C.; Foster, R. N. 1988.
Comparison of grasshopper population characteristics in relation
to grassland types in western North Dakota in 1987. In: Cooperative
Grasshopper Integrated Pest Management Project, 1988 annual report.
Boise ID, U.S. Department of Agriculture, Animal and Plant Health
Inspection Service: 244-252.
Kemp, W. P.; Onsager, J. A. 1994. Grasshopper population
response to modification of vegetation by grazing. In: Cooperative
Grasshopper Integrated Pest Management Project, 1994 annual report.
Boise, ID: U.S. Department of Agriculture, Animal and Plant Health
Inspection Service: 93-98.
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