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Description

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Distinguishing characters include a white or cream dorsal stripe and lack of cranial crest. This species has two known subspecies, Anaxyrus boreas boreas and A. b. halophilus. A. b. boreas is dusky gray or greenish above with warts set in dark blotches, often mixed with a bit of rusty color. Males are usually less blotched with smoother skin and are smaller than females (Stebbins 1985).It has been known to occasionally hybridize with the red-spotted toad (Anaxyrus punctatus) and the Canadian toad (Anaxyrus hemiophrys) (Stebbins 1985). See other subspecies accounts at www.californiaherps.com: B. b.boreas and B.b. halophilus .

References

  • Blaustein, A. R., Hoffman, P. D., Hokit, D. G., Kiesecker, J. M., Walls, S. C., and Hays, J. B. (1994). "UV repair and resistance to solar UV-B in amphibian eggs: A link to population declines?" Proceedings of the National Academy of Sciences of the United States of America, 91(5), 1791-1795.
  • Brown, L. E. and Littlejohn, M. J. (1971). ''Male release call in the Bufo americanus group.'' Evolution in the Genus Bufo. W. F. Blair, eds., University of Texas Press, Austin, 310-323.
  • Corn, P. S. (1998). "Effects of ultraviolet radiation on boreal toads in Colorado." Ecological Applications, 8, 18-26.
  • Duellman, W. E., and Trueb, L. (1986). Biology of Amphibians. McGraw-Hill, New York.
  • Kiesecker, J. M., and Blaustein, A. R. (1995). "Synergism between UV-B radiation and a pathogen magnifies amphibian embryo mortality in nature." Proceedings of the National Academy of Sciences of the United States of America, 92(24), 11049-11052.
  • Kiesecker, J. M., and Blaustein, A. R. (1997). "Influences of egg laying behavior on pathogenic infection of amphibian eggs." Conservation Biology, 11(1), 214-220.
  • Stebbins, R. C. (1985). A Field Guide to Western Reptiles and Amphibians. Houghton Mifflin, Boston.
  • Stebbins, R. C., and Cohen, N. W. (1995). A Natural History of Amphibians. Princeton University Press, Princeton, New Jersey.
  • Trenham, P. C., and Marsh, D. M. (2001). ''Amphibian translocation programs: reply to Seigel and Dodd.'' Conservation Biology, 16(2), 555-556.
  • Vertucci, F. A., and Corn, P. S. (1996). "Evaluation of episodic acidification and amphibian declines in the Rocky Mountains." Ecological Applications, 6(2), 449-457.

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Distribution and Habitat

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Populations of A. b. halophilus are found in California, w. Nevada, and n. Baja California. Populations of A. b. boreas are found in southern Alaska, British Columbia, Alberta, Washington, Oregon, Idaho, Montana, Wyoming, Colorado, northern California, Nevada, New Mexico, and Utah. This toad frequents a wide variety of habitats such as, desert streams, grasslands, woodlands, and mountain meadows, and can be found in or near a variety of water bodies (Stebbins 1985).
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Life History, Abundance, Activity, and Special Behaviors

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UV-B radiation has been shown to cause reduced hatching success in Oregon (Blaustein et al. 1994), but not in Colorado, although more investigation is needed (Corn 1998). Synergistic effects between UV-B and an alga, Saprolegnia ferax , have also been shown to cause reduced hatching success in Oregon (Kiesecker and Blaustein 1995). Vertucci and Corn (1993) found that acid precipitation may not be a major cause of the decline of A. b. boreas in Colorado, but more investigation of this problem is needed (Stebbins and Cohen 1995). A. boreas tends to lay its eggs in communal masses, and such communal egg masses have been shown to be highly susceptible to infection with S. ferax (Kiesecker and Blaustein 1997). In the southern Rocky Mountains, translocation was tried for A. b. boreas. The translocation projects failed; A. b. boreas has been declining in that area for unknown reasons, for some time (Trenham 2001).
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Life History, Abundance, Activity, and Special Behaviors

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This species is an explosive breeder. Females deposit thousands of eggs in long strings, usually in shallow ponds. These toads are nocturnal at low elevations and diurnal at higher elevations. During the winter, A. boreas buries itself in loose soil or uses the burrow of a small mammal (Stebbins 1985). This species tends to walk rather than hop. Both males and females lack an advertisement call (Duellman and Trueb 1986) although they are known to have a release call (Brown and Littlejohn 1971).
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Associated Plant Communities

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More info for the terms: bog, forest, woodland

The boreal toad is found in the Rocky Mountains in aspen (Populus spp.)
groves and riparian forests [8]. In Colorado, the largest populations
are typically found in areas characterized by willows (Salix spp.), bog
birch (Betula glandulosa), and shrubby cinquefoil (Potentilla fruticosa)
[41]. In the Pacific Northwest, the western toad occurs in mountain
meadows and less commonly in Douglas-fir forests (Pseudotsuga menziesii) [8].

In California, optimum habitat for the western toad includes wet or dry
mountain meadows or riparian deciduous forest with available open water
for breeding. Suitable habitat includes blue oak (Quercus douglasii)
savanna, gray pine-oak forest (Pinus sabiniana-Quercus spp.), mixed
conifer forest, and alpine meadows. Marginal habitats include annual
grasslands, chaparral, ponderosa pine forests, California black oak
woodlands, Jeffrey pine forests, and red fir forests [20].

In the Sierra Nevada, the western toad occurs in mid-elevation pine
forests (including Jeffrey pine [Pinus jeffreyi] at higher elevations
and ponderosa pine [Pinus ponderosa] at lower elevations), California
black oak woodlands [Quercus kelloggii], giant sequoia groves
(Sequoiadendron giganteum), montane fir forest (which includes white fir
[Abies concolor], red fir [A. magnifica], and western white pine [P.
monticola]), and redwood forest (Sequoia sempervirens). It is also
found in riparian areas within sagebrush-pinyon communities (Artemisia
spp.-Pinus spp.), oak-pine woodland and savanna (including coast live
oak [Q. agrifolia], interior live oak [Q. wislizenii], and canyon live
oak [Q. chrysolepis]), and California coastal forest and scrub [8].

Western toads have been collected from sedge meadows near a pond
occurring in a creosotebush (Larrea tridentata) community, and from
aspen (Populus spp.)-willow groves within big sagebrush
(Artemisia tridentata)-grassland [15].
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Sullivan, Janet. 1994. Anaxyrus boreas. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Common Names

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western toad
boreal toad
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Sullivan, Janet. 1994. Anaxyrus boreas. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Conservation Status

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Information on state- and province-level protection status of animals in the
United States and Canada is available at NatureServe.
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Sullivan, Janet. 1994. Anaxyrus boreas. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Cover Requirements

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More info for the terms: cover, forest

Western toads are terrestrial. Their body temperatures are largely
controlled by basking and evaporative cooling. In order to avoid
evaporative conditions, they usually spend the daylight hours on the
forest floor in the soil under rocks, logs, stumps, or other surface
objects or in rodent burrows [8,11,15,16,24]. Individuals have been
observed to use the same retreat repeatedly. In locations where there
is little or no hiding cover, western toads may spend most of the day in
the water [15]. Under more humid conditions, western toads may become
active during the day [11].

Breeding Cover: western toads lay their eggs in water; they require
some form of surface cover near the egg-laying location. Woody debris
or submerged vegetation is used to protect egg masses [10,24].
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Sullivan, Janet. 1994. Anaxyrus boreas. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Distribution

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The range of western toad extends from western British Columbia and
southern Alaska south through Washington, Oregon, and Idaho to northern
Baja California, Mexico; east to Montana, western and central Wyoming,
Nevada, the mountains and higher plateaus of Utah, and western Colorado
[15]. Occurrences of the boreal toad from Yukon Territory, the
Northwest Territories, and northwestern and north-central British
Columbia have been reported [36]. Southern records of boreal toads in
New Mexico have been published [35].

The ranges of subspecies are as follows [13,15]:

boreal toad: western British Colombia and southern Alaska south from
Washington, Oregon, Idaho, western Montana and western Wyoming to northern
California, Nevada, western Colorado, and western Utah.

California toad: extreme western Nevada through the Central Valley of
California and coastal California south to Baja California Norte.
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Sullivan, Janet. 1994. Anaxyrus boreas. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Food Habits

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Western toads wait for their prey on the surface of the ground or in
shallow burrows dug by other animals. Their diet consists largely of
bees, beetles, ants, and arachnids. Other foods include crayfish,
sowbugs, grasshoppers, trichopterans, lepidopterans, and dipterans
[15,20].
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Sullivan, Janet. 1994. Anaxyrus boreas. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Habitat-related Fire Effects

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More info for the terms: cover, top-kill

Western toads occupy diverse habitats, some of which experience fire
relatively frequently (Douglas-fir forests in drier areas [31]), and
some of which rarely experience fire (riparian zones tend to act as fire
breaks but will burn during extended dry conditions [30]).

No specific information describing the response of western toads and
their habitat to fire was available in the literature. Western toads
are vulnerable to changes in both terrestrial and aquatic habitat. They
are, however, found in slightly higher abundance in early seres of
Douglas-fir forests [28]. Severe fires that burn surface objects such
as logs and stumps would immediately decrease available hiding cover for
western toads, but postfire sprouting of shrubby species would result in
a longer-term, overall increase in low hiding cover [30]. Most willow
species sprout after top-kill by fire [29], so the amount and thickness
of willow clumps increases after fire. Crown fires would reduce shade
and surface humidity and decrease the amount of daylight time toads
could spend active after a fire. Fires during early spring could affect
egg masses by reducing shade and increasing water temperatures. Any
substantial change in runoff rates, erosion, or water tables caused by
fire could degrade breeding sites.

It is likely that there is a change in the relative amounts of different
types of prey organisms in the postfire diet of western toads.
Immediately after fire, many insects are present but those requiring
shade do not adapt well to the more open conditions. In the longer term
there are differential responses to fire among prey organisms; ant
populations were one-third higher in burned areas than in unburned
areas, but beetles tend to decrease on burned areas [32].
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Sullivan, Janet. 1994. Anaxyrus boreas. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Habitat: Cover Types

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This species is known to occur in association with the following cover types (as classified by the Society of American Foresters):

207 Red fir
211 White fir
215 Western white pine
217 Aspen
222 Black cottonwood - willow
229 Pacific Douglas-fir
230 Douglas-fir - western hemlock
239 Pinyon - juniper
241 Western live oak
243 Sierra Nevada mixed conifer
246 California black oak
247 Jeffrey pine
250 Blue oak - Digger pine
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Sullivan, Janet. 1994. Anaxyrus boreas. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Habitat: Ecosystem

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This species is known to occur in the following ecosystem types (as named by the U.S. Forest Service in their Forest and Range Ecosystem [FRES] Type classification):

More info for the term: shrub

FRES20 Douglas-fir
FRES21 Ponderosa pine
FRES22 Western white pine
FRES23 Fir-spruce
FRES24 Hemlock-Sitka spruce
FRES25 Larch
FRES27 Redwood
FRES28 Western hardwoods
FRES29 Sagebrush
FRES30 Desert shrub
FRES34 Chaparral-mountain shrub
FRES35 Pinyon-juniper
FRES36 Mountain grasslands
FRES37 Mountain meadows
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Sullivan, Janet. 1994. Anaxyrus boreas. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Habitat: Plant Associations

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This species is known to occur in association with the following plant community types (as classified by Küchler 1964):

More info for the terms: forest, woodland

K001 Spruce - cedar - hemlock forest
K002 Cedar - hemlock - Douglas-fir forest
K003 Silver fir - Douglas-fir forest
K005 Mixed conifer forest
K006 Redwood forest
K007 Red fir forest
K011 Western ponderosa forest
K012 Douglas-fir forest
K014 Grand fir - Douglas-fir forest
K018 Pine - Douglas-fir forest
K023 Juniper - pinyon woodland
K025 Alder - ash forest
K029 California mixed evergreen forest
K030 California oakwoods
K038 Great Basin sagebrush
K041 Creosotebush
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Sullivan, Janet. 1994. Anaxyrus boreas. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Management Considerations

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More info for the term: forest

Reproductive success of western toads depends on amount of snowpack and
rate of snowmelt which determine the persistence of breeding pools used
by western toad populations [33].

Amphibians generally seem to be more sensitive to environmental changes
than other taxonomic groups. Western toads repeatedly use individual
stumps or logs, which may be an important consideration for conservation
and recovery programs. They are also vulnerable to mass predation by
common ravens during breeding periods when large numbers of toads
congregate at egg-laying sites. It was observed that such mass
predation did not occur when humans were in close proximity to the
toads. The authors speculated that human activity may play a role in
common raven activity pattern, and could contribute indirectly to mass
predation episodes. Since the entire breeding effort of a population is
concentrated in one location, mass predation on eggs can have severe
consequences to population recruitment. The eggs are also vulnerable to
catastrophic loss due to freezing, lowering of water levels, and other
disturbances. Human activities such as logging and/or prescribed
burning may have a negative effect on breeding congregations or on
massed eggs by reducing woody debris in and near the water, reducing
available shade, and pressuring predators to move from human activity
sites to sites where western toad breeding is occurring [10].

In northwestern California, however, western toads were slightly more
abundant in early brush/sapling stages of postharvest Douglas-fir forest
compared to later stages or undisturbed forest; they are therefore
classified as increasers after logging [28]. The water level of
breeding pools could also be affected by human activity at critical
times. The absence of nonbreeding adult females from breeding
congregations provides some protection (at the population level) from
population decline due to mass predation. More than half of females
skipped at least 1 year between breeding years at study sites in the
Oregon Cascade Range [10].

Mortality of western toads is greatest during the larval and juvenile
stages, but is slight thereafter. Most mortality can be attributed to
unseasonable weather and predation on juvenile toads. There is very
little predation on adult toads and mortality of adults is low [41].

Western toads are taken by humans for the pet trade [23].
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Sullivan, Janet. 1994. Anaxyrus boreas. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Occurrence in North America

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AK
CA
CO
ID
MT
NV
NM
OR
UT
WA
WY

BC

Mexico
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Sullivan, Janet. 1994. Anaxyrus boreas. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Predators

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Tadpoles are preyed upon by fish, herpetiles, birds, and mammals [11].

Toads in general tend to walk or hop rather than jump (like frogs).
Their slow movement renders them vulnerable to predators; however, the
western toad (like other toads) produces skin toxins that are avoided by
many predator species. The nocturnal habit may help reduce predation
[8]. Adult western toads are preyed upon by common ravens (Corvus
corvax) and probably by other birds, herpetiles, and mammals as well
[10,11]. A badger (Taxidea taxus) was recorded as having consumed five
adult Anaxyrus (probably western toad, as it was the only Anaxyrus species in
the area) in Wyoming [37].
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Sullivan, Janet. 1994. Anaxyrus boreas. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Preferred Habitat

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Western toads are widespread throughout the mountainous areas of
northwestern North America, ranging from sea level to elevations near or
above regional treeline, or 10,000 feet (305-3,050 m) in elevation
[15,20]. It is uncommon at the higher elevations [20]. Elevational
range in Colorado is from about 7,000 feet to 11,860 feet (2,131-3615
m). In the mountains of Colorado, the largest western toad populations
usually occur from about 9,500 feet to 11,000 feet (2,896-3,353 m)
elevation [34]. Western toads occupy desert streams and springs,
grasslands, and mountain meadows; they are less common in heavily wooded
regions. They are usually found in or near ponds, lakes (including
saline lakes), reservoirs, rivers, and streams within the above
mentioned habitats [15,16]. Under laboratory conditions western toads
were able to survive in 40 percent seawater, but died within a week when
exposed to 50 percent seawater [11].

In Colorado, individual western toads typically maintain distinct ranges
which vary greatly in size according to the condition of the habitat.
Breeding males may exhibit territoriality, especially in areas where
breeding sites are scarce [41].

Populations of western toads have very limited dispersal, particularly
in rugged terrain [10].

Breeding Habitat: Western toads require open water for breeding [20].
All breeding members of a local population tend to lay their eggs in the
same location, which is used repeatedly from year to year. For example,
at one site on a permanent lake in the Oregon Cascade Range, western
toads returned each year to the same submerged willow clumps [10]. Eggs
are usually laid in shallow water (not deeper than 12 inches [30 cm] but
usually at least 6 inches [15 cm]) [10,24]. The warmth of shallow water
increases the rate at which development occurs; shallow water and
vegetative matter may contribute to protection of eggs from predation by
fish [10]. In western Montana, breeding western toads used gravel pits
that were only filled with water during spring runoff. These gravel
pits contained cattails (Typha spp.) but no other vegetation, and were 5
feet (1.5 m) deep in the center [33].
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Sullivan, Janet. 1994. Anaxyrus boreas. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Regional Distribution in the Western United States

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This species can be found in the following regions of the western United States (according to the Bureau of Land Management classification of Physiographic Regions of the western United States):

1 Northern Pacific Border
2 Cascade Mountains
3 Southern Pacific Border
4 Sierra Mountains
5 Columbia Plateau
6 Upper Basin and Range
8 Northern Rocky Mountains
9 Middle Rocky Mountains
10 Wyoming Basin
11 Southern Rocky Mountains
12 Colorado Plateau
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Sullivan, Janet. 1994. Anaxyrus boreas. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Synonyms

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Bufo boreas Baird and Girard [13,16]

ORDER:
Anura
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Sullivan, Janet. 1994. Anaxyrus boreas. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Taxonomy

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The currently accepted scientific name for western toad is Anaxyrus boreas
(Baird and Girard) (Bufonidae). Accepted subspecies are as follows [41,42]:

Anaxyrus boreas subsp. boreas boreal toad
Anaxyrus boreas subsp. halophilus (Baird and Girard) California toad, alkali toad
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Sullivan, Janet. 1994. Anaxyrus boreas. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Timing of Major Life History Events

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More info for the terms: habitat type, hibernaculum, hibernation, natural

Seasonal Activity: Western toads are active from January to October,
depending on latitude and elevation [16]. Boreal toads in one Colorado
population used natural chambers near a small stream bed. The high
water table, constantly flowing stream, and deep winter snow served to
maintain the air temperature within the hibernaculum at a point slightly
above freezing. Emergence from hibernation followed a few days of warm
temperatures that freed the entrance and increased temperatures within
the chamber to about 39.2 degrees Fahrenheit (4 deg C) [40,41].

Diurnal Activity: At low elevations western toads are active at night;
at high elevations and in the northern parts of their range they are
diurnal [16]. Body temperature of western toads is closely correlated
with the substrate temperature. Basking and conduction from the
substrate are primary means of increasing body temperature and cooling
is achieved by evaporative cooling and conduction of heat to a cooler
medium. Diurnal and nocturnal activity are often related to seasonal
changes in temperature; most western toads are diurnal during the spring
and fall but are nocturnal during the warmer summer months [41].

Minimum Breeding Age: In central Oregon, the minimum breeding age for
male western toads is 3 years, and probably 4 or 5 years for females
[10]. California toads are reported as sexually mature at 2 years of
age [11]. Male western toads breed every year; females breed at less
regular intervals, depending on individual condition and previous years'
breeding effort [10]. Sex ratios differ according to habitat type;
males are more numerous in wet areas and females are more numerous in
dry habitats [41].

Breeding Season: Eggs are laid in open water from February to July,
with peak activity occurring in April. Timing of egg-laying activity
varies with elevation and weather conditions [20]. In Colorado,
initiation of breeding was correlated with the onset of warming weather
and initiation of snowpack melting. Eggs are usually laid in late May
or early June [41]. In western Montana, a few males were present on the
shores (of two gravel pits) by May 11, 1967, and by May 14, each pond
contained at least 30 males. Males were spaced at least 1 foot (.3 m)
apart, all facing the shore [33].

Clutch Size: Eggs are laid in gelatinous strings of 13 to 52 eggs per
inch, in masses of up to 16,500 per clutch [15,24]. Egg development
rate is partially dependent on temperature; hatching times vary [11].

Development of Young: Metamorphosis is usually completed within 3
months of egg laying. The time required for metamorphosis is given as
30 to 45 days for the boreal toad and 28 to 45 days for the California
toad [15].

Longevity: Female western toads at least 10 to 11 years of age have
been reported [10]. In Colorado, boreal toads probably attain a maximum
age of at least 9 years [41].
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Sullivan, Janet. 1994. Anaxyrus boreas. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

U.S. Federal Legal Status

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None [43]
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Sullivan, Janet. 1994. Anaxyrus boreas. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Use of Fire in Population Management

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More info for the terms: cover, fire regime, prescribed fire

Specific information concerning prescribed fire as it affects western
toads was not available in the literature. Conservation of surface
objects used for hiding cover is important in any management decision
[10].

FIRE REGIMES :
Find fire regime information for the plant communities in which this
species may occur by entering the species name in the FEIS home page under
"Find FIRE REGIMES".
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Sullivan, Janet. 1994. Anaxyrus boreas. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Western toad

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The western toad (Anaxyrus boreas) is a large toad species, between 5.6 and 13 cm (2.2 and 5.1 in) long, native to western North America.[1][3][4] A. boreas is frequently encountered during the wet season on roads, or near water at other times. It can jump a considerable distance for a toad. Breeding occurs between March and July in mountainous areas, and as early as January in lower-elevation regions. The female lays up to 17,000 eggs stuck together in strings that adhere to vegetation and other objects along water edges.[5]

Description

It has a white or cream dorsal stripe, and is dusky gray or greenish dorsally with skin glands concentrated within the dark blotches. Its parotoid glands are oval, widely separated, and larger than the upper eyelids. It has a mottled venter and horizontal pupils but lacks cranial crests. Compared to females, males have smoother skin, reduced dorsal blotching, and nuptial pads (thickened skin) on their forefeet during breeding season. In juveniles of this species, the dorsal stripe is weak or absent. Large young have prominent dorsal and ventral spotting and yellow feet.

Subspecies

There are two known subspecies of the western toad and the ranges of subspecies are as follows:[6][7]

Distribution

The range of the western toad extends from western British Columbia and southern Alaska south through Washington, Oregon, and Idaho to northern Baja California, Mexico; east to Montana, western and central Wyoming, Nevada, the mountains and higher plateaus of Utah, and western Colorado.[6] Occurrences of the boreal toad from Yukon Territory, the Northwest Territories, and northwestern and north-central British Columbia have been reported.[8] Southern records of boreal toads in New Mexico have been published, [9] but the species is considered extirpated from the state, with a reintroduction in progress.[1]

Habitat

The boreal toad is found in the Rocky Mountains in aspen (Populus spp.) groves and riparian forests.[10] In Colorado, the largest populations are typically found in areas characterized by willows (Salix spp.), bog birch (Betula glandulosa), and shrubby cinquefoil (Potentilla fruticosa).[11] In the Pacific Northwest, the western toad occurs in mountain meadows and less commonly in Douglas-fir forests (Pseudotsuga menziesii).[10]

In California, optimum habitat for the western toad includes wet or dry mountain meadows or riparian deciduous forest with available open water for breeding. Suitable habitat includes blue oak (Quercus douglasii) savanna, gray pine-oak forest (Pinus sabiniana-Quercus spp.), mixed conifer forest, and alpine meadows. Marginal habitats include annual grasslands, chaparral, ponderosa pine forests, California black oak woodlands, Jeffrey pine forests, and red fir forests.[12]

In the Sierra Nevada, the western toad occurs in mid-elevation pine forests (including Jeffrey pine (Pinus jeffreyi) at higher elevations and ponderosa pine (Pinus ponderosa) at lower elevations), California black oak woodlands (Quercus kelloggii), giant sequoia groves (Sequoiadendron giganteum), montane fir forest (which includes white fir (Abies concolor), red fir (Abies magnifica), and western white pine (Pinus monticola), and redwood forest (Sequoia sempervirens). It is also found in riparian areas within sagebrush-pinyon communities (Artemisia spp.-Pinus spp.), oak-pine woodland and savanna (including coast live oak (Quercus agrifolia), interior live oak (Quercus wislizenii), and canyon live oak (Quercus chrysolepis), and California coastal forest and scrub.[10]

Western toads have been collected from sedge meadows near a pond occurring in a creosotebush (Larrea tridentata) community, and from aspen (Populus spp.)-willow groves within big sagebrush (Artemisia tridentata)-grassland.[6]

Life cycle

Oval parotoid glands, located behind the eyes, are distinguishing features of this species.

Western toads are active from January to October, depending on latitude and elevation, and hibernate over the winter.[13] Boreal toads in one Colorado population used natural chambers near a small stream bed. The high water table, constantly flowing stream, and deep winter snow served to maintain the air temperature within the hibernaculum at a point slightly above freezing. Emergence from hibernation followed a few days of warm temperatures that freed the entrance and increased temperatures within the chamber to about 39.2 °F (4.0 °C).[11][14]

At low elevations western toads are active at night; at high elevations and in the northern parts of their range they are diurnal.[13] Body temperature of western toads is closely correlated with the substrate temperature. Basking and conduction from the substrate are primary means of increasing body temperature and cooling is achieved by evaporative cooling and conduction of heat to a cooler medium. Diurnal and nocturnal activity are often related to seasonal changes in temperature; most western toads are diurnal during the spring and fall but are nocturnal during the warmer summer months.[11]

In central Oregon, the minimum breeding age for male western toads is three years, and probably four or five years for females.[15] California toads are reported as sexually mature at 2 years of age.[16] Male western toads breed every year; females breed at less regular intervals, depending on individual condition and previous years' breeding effort.[15] Sex ratios differ according to habitat type; males are more numerous in wet areas and females are more numerous in dry habitats.[11]

Eggs are laid in open water from February to July, with peak activity occurring in April. Timing of egg-laying activity varies with elevation and weather conditions.[12] In Colorado, initiation of breeding was correlated with the onset of warming weather and initiation of snowpack melting. Eggs are usually laid in late May or early June.[11] In western Montana, a few males were present on the shores (of two gravel pits) by May 11, 1967, and by May 14, each pond contained at least 30 males. Males were spaced at least 1 foot (0.30 m) apart, all facing the shore[17] Eggs are laid in gelatinous strings of 13 to 52 eggs per inch (2.5 cm), in masses of up to 16,500 per clutch.[6][18] Egg development rate is partially dependent on temperature; hatching times vary.[16]

Metamorphosis is usually completed within three months of egg laying. The time required for metamorphosis is given as 30 to 45 days for the boreal toad and 28 to 45 days for the California toad.[6]

Female western toads at least 10 to 11 years of age have been reported.[15] In Colorado, boreal toads probably attain a maximum age of at least 9 years.[11]

Preferred habitat

Western toads are widespread throughout the mountainous areas of northwestern North America, ranging from sea level to elevations near or above regional treeline, or 10,000 feet (305–3,050 m) in elevation.[6][12] It is uncommon at the higher elevations.[12] Elevational range in Colorado is from about 7,000 to 11,860 feet (2,130 to 3,610 m). In the mountains of Colorado, the largest western toad populations usually occur from about 9,500 to 11,000 feet (2,900 to 3,400 m) elevation.[19] Western toads occupy desert streams and springs, grasslands, and mountain meadows; they are less common in heavily wooded regions. They are usually found in or near ponds, lakes (including saline lakes), reservoirs, rivers, and streams within the above-mentioned habitats.[6][13] Under laboratory conditions western toads were able to survive in 40% seawater, but died within a week when exposed to 50% seawater.[16]

In Colorado, individual western toads typically maintain distinct ranges which vary greatly in size according to the condition of the habitat. Breeding males may exhibit territoriality, especially in areas where breeding sites are scarce.[11]

Populations of western toads have very limited dispersal, particularly in rugged terrain.[15]

Western toads require open water for breeding.[12] All breeding members of a local population tend to lay their eggs in the same location, which is used repeatedly from year to year. For example, at one site on a permanent lake in the Oregon Cascade Range, western toads returned each year to the same submerged willow clumps.[15] Eggs are usually laid in shallow water, not deeper than 12 inches (300 mm) but usually at least 6 inches (150 mm).[15][18] The warmth of shallow water increases the rate at which development occurs; shallow water and vegetative matter may contribute to protection of eggs from predation by fish.[15] In western Montana, breeding western toads used gravel pits that were only filled with water during spring runoff. These gravel pits contained cattails (Typha spp.) but no other vegetation, and were 5 feet (1.5 m) deep in the center.[17]

Cover requirements

Western toads are terrestrial. Their body temperatures are largely controlled by basking and evaporative cooling. In order to avoid evaporative conditions, they usually spend the daylight hours on the forest floor in the soil under rocks, logs, stumps, or other surface objects or in rodent burrows.[6][10][13][16][18] Individuals have been observed to use the same retreat repeatedly. In locations where there is little or no hiding cover, western toads may spend most of the day in the water.[6] Under more humid conditions, western toads may become active during the day.[16]

Western toads lay their eggs in water; they require some form of surface cover near the egg-laying location. Woody debris or submerged vegetation is used to protect egg masses.[15][18]

Food habits

Western toads wait for their prey on the surface of the ground or in shallow burrows dug by other animals. Their diet consists largely of bees, beetles, ants, and arachnids. Other foods include crayfish, sow bugs, grasshoppers, trichopterans, lepidopterans, and dipterans.[6][12]

Predators

Tadpoles are preyed upon by fish, reptiles, amphibians, birds, and mammals.[16] Toads in general tend to walk or hop rather than jump (like frogs). Their slow movement renders them vulnerable to predators; however, the western toad (like other toads) produces skin toxins that are avoided by many predator species. The nocturnal habit may help reduce predation.[10] Adult western toads are preyed upon by common ravens (Corvus corax) and probably by other birds, reptiles, amphibians, and mammals as well.[15][16] A badger (Taxidea taxus) was recorded as having consumed five adult Anaxyrus (probably western toad, as it was the only Anaxyrus species in the area) in Wyoming.[20]

Conservation

The western toad occupies a variety of habitats and is presently listed as a species of least concern.[1] Nonetheless, concerns remain about the impact of disease and chemical contamination of the environment, especially chytridiomycosis. One of the chief chemical threats is the overuse of urea as fertilizer, which is often applied in high dosage to forest environments to increase biomass productivity and economic return. A. boreas is harmed by the dermal absorption of this chemical, which can lead to increased mortality.[21]

References

Public Domain This article incorporates public domain material from Bufo boreas. United States Department of Agriculture.

  1. ^ a b c d IUCN SSC Amphibian Specialist Group. 2022. Anaxyrus boreas. The IUCN Red List of Threatened Species 2022: e.T181488862A197445871. Accessed on 15 December 2022.
  2. ^ "Anaxyrus boreas. NatureServe Explorer 2.0". explorer.natureserve.org. Retrieved 15 December 2022.
  3. ^ Frost, Darrel R. (2016). "Anaxyrus boreas (Baird and Girard, 1852)". Amphibian Species of the World: an Online Reference. Version 6.0. American Museum of Natural History. Retrieved 6 February 2016.
  4. ^ "Anaxyrus boreas". AmphibiaWeb: Information on amphibian biology and conservation. [web application]. Berkeley, California: AmphibiaWeb. 2016. Retrieved 6 February 2016.
  5. ^ Grismer, L. L. (2002). Amphibians and Reptiles of Baja California. Los Angeles: University of California Press, p. 66, ISBN 0520925203.
  6. ^ a b c d e f g h i j Stebbins, R. C. (1951) Amphibians of western North America. Berkeley, CA: University of California Press
  7. ^ Schmidt, Karl P. 1953. A checklist of North American amphibians and reptiles. 6th ed. Chicago, IL: University of Chicago Press; American Society of Ichthyologists and Herpetologists
  8. ^ Long, Charles A. (1964). "The badger as a natural enemy of Ambystoma tigrinum and Anaxyrus boreas". Herpetologica. 20 (2): 144.
  9. ^ Cook, Francis R. (1977). "Records of the boreal toad from the Yukon and northern British Columbia". Canadian Field-Naturalist. 91: 185–186.
  10. ^ a b c d e Kricher, John C. (1993) A field guide to the ecology of western forests. The Peterson Field Guide Series No. 45. Boston, MA: Houghton Mifflin Company
  11. ^ a b c d e f g U.S. Department of the Interior, Fish and Wildlife Service. (1994). Endangered and threatened wildlife and plants; animal candidate review for listing as endangered or threatened species; proposed rule. 50 CFR Part 17. Tuesday, November 15, 1994. Federal Register. 59(219): 58982-59028
  12. ^ a b c d e f Verner, Jared; Boss, Allan S., tech. coords. (1980). California wildlife and their habitats: western Sierra Nevada. Gen. Tech. Rep. PSW-37. Berkeley, CA: U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station
  13. ^ a b c d Stebbins, R. C. (1985) Western reptiles and amphibians. 2nd ed. Peterson Field Guides No. 16. Boston: Houghton Mifflin Company
  14. ^ Campbell, James B. (1970). Life history of Bufo boreas boreas on the Colorado Front Range. Boulder, CO: University of Colorado, Biology Department. Dissertation. In: Dissertation Abstracts. 33: 3331B
  15. ^ a b c d e f g h i Olson, Deanna H. (1992) "Ecological susceptibility of amphibians to population declines". In: Harris, Richard R.; Erman, Don C.; Kerner, Hannah M. Proceedings of the symposium on biodiversity of northwestern California; 1991 October 28–30; Santa Rosa, CA. Report 29. Berkeley, CA: University of California, Division of Agriculture and Natural Resources, Wildland Resources Center: pp. 55–62
  16. ^ a b c d e f g Porter, Kenneth R. (1972) Herpetology. Philadelphia, PA: W. B. Sanders Company, ISBN 0721672957.
  17. ^ a b Campbell, James B. (1976) "Environmental controls on boreal toad populations in the San Juan Mountains". In: Steinhoff, Harold W.; Ives, Jack D., eds. Ecological impacts of snowpack augmentation in the San Juan Mountains, Colorado. Final report San Juan ecology project. Fort Collins, CO: Colorado State University Publication: pp. 289–295
  18. ^ a b c d Kahn, Walter C. (1960). "Observations on the effect of a burn on a population of Sceloporus occidentalis". Ecology. 41 (2): 358–359. doi:10.2307/1930227. JSTOR 1930227.
  19. ^ Campbell, James B.; Degenhardt, William G. (1971). "Bufo boreas boreas in New Mexico". The Southwestern Naturalist. 16 (2): 219. doi:10.2307/3670507. JSTOR 3670507.
  20. ^ Martin, Robert F. (1973). "Osteology of North American bufo: the americanus, cognatus, and boreas species groups". Herpetologica. 29 (4): 375–387. JSTOR 3891581.
  21. ^ Hogan, C. Michael (2008) Rough-skinned Newt (Taricha granulosa), Globaltwitcher, ed. N. Stromberg
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Western toad: Brief Summary

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The western toad (Anaxyrus boreas) is a large toad species, between 5.6 and 13 cm (2.2 and 5.1 in) long, native to western North America. A. boreas is frequently encountered during the wet season on roads, or near water at other times. It can jump a considerable distance for a toad. Breeding occurs between March and July in mountainous areas, and as early as January in lower-elevation regions. The female lays up to 17,000 eggs stuck together in strings that adhere to vegetation and other objects along water edges.

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