dcsimg

Description

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A small toad of the family Pelobatidae, the genus is characteristically short-legged and squat, having vertical "cat-eye" pupils, and a black, keratinized spade (used for burrowing) on the underside of each hind foot.Their skin is relatively smooth compared to the rough, warty epidermis of truetoads (genus Bufo). Females are slighty larger than males. Distinguishing features include a slightly upturned, "pug-nose", a raised callus, or boss, between the eyes, and a dark brown or orange spot on each upper eyelid. Dorsal coloration is similar to that of other Spea and Scaphiopus species: Usually a brown, gray, or olive background, mottled with darker spots posessing light-colored centers. The ground color is variable and often matches the substrate. The venter is light gray, white, or creamy. Tadpoles have large, globular or ovoid bodies, reaching 70 mm in total length. Their dorsal coloration is black, brown, or dark gray and flecked with metallic golds and rusts, while the abdomen displays an overall golden irridescence. The spiracle is located low on the abdomen, and to the left side.
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Distribution and Habitat

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This species lives in western North America, in the United States and Canada. In Calfornia, they occur east of the Sierra Nevada, and north of San Bernardino Co. They occur throughout Nevada and Utah east of the Colorado River, push just south into northwest Arizona, and north into northwest Colorado and southwest Wyoming. In Canada, Washington and Oregon, they are sandwiched between the Cascade and Rocky Mtn. ranges, but occur throughout lower Idaho. They are found in arid regions, often associated with high desert scrub and sagebrush, but also reach past the pinion-juniper woodland, and into the spruce-fir belt at about 2800 m (9200 ft). Little is known about abundance due, in part, to its explosive breeding habits, but it is often heard in temporary pools and flooded ditches immediately after winter and spring rains. Activity varies with local conditions, but it is most active during and after winter, spring, and sometimes summer rains, when it may emerge to breed or forage on wet nights.
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Life History, Abundance, Activity, and Special Behaviors

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Officially unthreatened, but recent studies have detected possible declines (Orchard 1992) and a repeat survey of historic collecting sites in the Sierra Nevada (Drost and Fellers 1996) found no specimens of Spea intermontana.
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Life History, Abundance, Activity, and Special Behaviors

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An explosive, opportunistic breeder, Spea intermontana is well adapted to the unpredictable and usually harsh seasons typical of the high desert areas it inhabits. Males have loud calls which attract females and probably other males to temporary or vernal pools where breeding takes place. Males are non-territorial, clumping and calling to females from partially submerged positions near the shore of pools. They appear to engage in a mad scramble for mates as they arrive. After breeding, adults disappear underground by using the spades on their hindfeet to burrow backward into the soil, thereby avoiding evaporative water loss to the dry desert air. Eggs are laid underwater in groups of 10-40, and depending on the type of vegetation and substrate available, are arranged in either flat sheets, short strings, or golfball sized clusters. Tadpoles may be either herbivorous or carnivorous, depending on local environmental conditions. The carnivorous morph has an enormous head, large jaw adductor muscles, and a sharp keratinous beak for tearing and cutting flesh. Tadpoles develop quickly to avoid dessication in their rapidly drying temporary pools.
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Lifespan, longevity, and ageing

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Maximum longevity: 20 years (wild) Observations: While the average longevity of this animal is certainly much shorter, it has been suggested that dormant animals may have survived over 20 years in the arid Imperial Valley (http://www.fs.fed.us/database/feis/).
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Conservation Status

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Total adult population size is not knows but exceeds 10,000. The species has no special conservation status and populations seem to be stable. Natural habitats have mostly not been subject to threat, though agriculture has reduced and threatened some populations. Irrigation, however, could be creating new habitats, as it creates standing water sources necessary for breeding in areas previously inhospitable to the toads. Man-made reservoirs also account for a sizable number of breeding sites. The fact that the toads are generalized in their feeding habits is also good news for the survival of the species; the elimination or reduction of a particular species of prey will not significantly impact the availability of food. In general, Great Basin spadefoot toads have a good chance of survival wherever standing water is available and wherever soil allows for burrowing.

US Federal List: no special status

CITES: no special status

IUCN Red List of Threatened Species: least concern

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Kadi, B. 2012. "Spea intermontana" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Spea_intermontana.html
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Bassel Kadi, University of Michigan-Ann Arbor
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Phil Myers, University of Michigan-Ann Arbor
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Rachelle Sterling, Special Projects
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Catherine Kent, Special Projects
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Associations

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Adult Great Basin spadefoot toads are preyed upon by western rattlesnakes, coyotes, and burrowing owls. Tadpoles are mainly preyed upon by western terrestrial garter snakes and American crows. When water levels rise high enough to flood breeding pools, tadpoles are also preyed upon by rainbow trout and brown trout.

When threatened, adult Great Basin spadefoot toads can produce noxious skin secretions, which are reported to smell like popcorn or roasted peanuts. The skin secretions are probably poisonous or at least distasteful to predators. They may even cause minor allergic reactions in humans, symptoms of which may include sneezing and a runny nose, and may also cause a burning sensation upon contact with the eyes and nose. Burrowing and camouflaged coloration may also help adult spadefoots escape predation. By contrast, tadpoles are comparatively helpless and have few defenses against predation other than cryptic coloration.

Known Predators:

  • western rattlesnakes (Crotalus viridis)
  • coyotes (Canis latrans)
  • burrowing owls (Athene cunicularia)
  • western terrestrial garter snakes (Thamnophis elegans)
  • American crows (Corvus brachyrhynchos)
  • rainbow trout (Oncorhynchus mykiss)
  • brown trout (Salmo trutta)

Anti-predator Adaptations: cryptic

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Kadi, B. 2012. "Spea intermontana" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Spea_intermontana.html
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Bassel Kadi, University of Michigan-Ann Arbor
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Phil Myers, University of Michigan-Ann Arbor
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Rachelle Sterling, Special Projects
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Catherine Kent, Special Projects
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Morphology

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Great Basin spadefoot toads usually have a gray, olive, or brown colored dorsal coloration mottled with darker spots with light-colored centers. Gray streaks outline an hourglass shaped marking on the back. The coloration is similar to that of other species of the genera Spea and Scaphiopus. Ventral coloration is light gray, white, or creamy and without markings. The skin is relatively smooth compared to the rough, warty nature of true toads (genus Bufo), but still contains small bumps. Parotoid glands seem to be absent. There is a dark brown or orange spot present on each upper eyelid. Pupils are vertical, and the eyes are large, catlike, golden yellow, and located on the side of the head. The nose is slightly upturned and there is a raised callus between the eyes. The body is short and fat with stubby limbs. Spadefoot toads get their name from the presence of a black, keratinized spade, or tubercle, on the underside of each hind foot, which is used for burrowing behavior. Adult body lengths vary from 32 to 67 mm and females tend to be only slightly larger than males. Tadpoles have large globular bodies and can reach 70 mm in length. They are colored black, brown, and gaey with scattered golden specks. When threatened, adult Great Basin spadefoot toads can produce noxious skin secretions, which are probably poisonous or at least distasteful to predators.

Range length: 32 to 67 mm.

Other Physical Features: ectothermic ; heterothermic ; bilateral symmetry ; poisonous

Sexual Dimorphism: sexes alike; female larger

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Kadi, B. 2012. "Spea intermontana" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Spea_intermontana.html
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Bassel Kadi, University of Michigan-Ann Arbor
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Phil Myers, University of Michigan-Ann Arbor
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Rachelle Sterling, Special Projects
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Catherine Kent, Special Projects
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Life Expectancy

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The lifespan of Great Basin spadefoot toads is unknown. It is assumed to be similar to other spadefoot toad species and is therefore estimated to be about 13 years for females and 11 years for males in the wild.

Typical lifespan
Status: wild:
11 to 13 years.

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Kadi, B. 2012. "Spea intermontana" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Spea_intermontana.html
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Bassel Kadi, University of Michigan-Ann Arbor
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Phil Myers, University of Michigan-Ann Arbor
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Rachelle Sterling, Special Projects
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Catherine Kent, Special Projects
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Habitat

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Great Basin spadefoot toads are found in arid regions, semi-desert shrubland, or sagebrush flats, but can also be found in alkali flats, pinion-juniper woodland, ponderosa pine, and high elevation spruce-fir forests at about 2800 m (9200 ft). Great Basin spadefoot toads require temporary or permanent water sources for breeding, such as slow-flowing springs, seasonal pools, irrigation ditches, and ponds. They are able to survive in arid habitats by remaining buried underground, thus their survival requires soils that permit burrowing.

Range elevation: 2800 (high) m.

Habitat Regions: temperate ; terrestrial

Terrestrial Biomes: desert or dune ; chaparral ; forest ; scrub forest ; mountains

Aquatic Biomes: temporary pools

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Kadi, B. 2012. "Spea intermontana" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Spea_intermontana.html
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Bassel Kadi, University of Michigan-Ann Arbor
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Phil Myers, University of Michigan-Ann Arbor
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Rachelle Sterling, Special Projects
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Catherine Kent, Special Projects
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Distribution

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Great Basin spadefoot toads are found in the United States and Canada. The species occurs in northwest Arizona, in California east of the Sierra Nevada mountain range, northwestern Colorado, lower Idaho, southwestern Wyoming, throughout Nevada and Utah, and between the Cascade and Rocky Mountain ranges in Oregon, Washington, and British Columbia.

Biogeographic Regions: nearctic (Native )

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Kadi, B. 2012. "Spea intermontana" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Spea_intermontana.html
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Bassel Kadi, University of Michigan-Ann Arbor
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Phil Myers, University of Michigan-Ann Arbor
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Rachelle Sterling, Special Projects
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Catherine Kent, Special Projects
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Trophic Strategy

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Adult Great Basin spadefoot toads are insectivores and carnivores who feed primarily at night. They are generalists, feeding on easily captured terrestrial insects and other arthropods. One study found that adult toads consumed at least 56 different arthropod taxa from the orders Coleoptera, Diptera, Hemiptera, Hymenoptera, Lepidoptera, Neuroptera, Orthoptera, Trichoptera, Collembola, and Araneae. Due to their abundance in the native habitats of Great Basin spadefoot toads, ants and darkling beetles are the most common sources of prey. Great Basin spadefoots do not have any particular preference, however, for one prey type over another. Toads are limited to eating species small enough for them to swallow whole, and tend not to eat species that produce noxious secretions, such as certain types of ground beetles. While plant matter has been found in the stomach contents of the toads, vegetation is not a primary source of food for adults of the species.

Little information is available regarding the feeding habits of Great Basin spadefoot toad larva. Tadpoles of spadefoot toads are omnivorous; they feed on water-born plant material such as algae, organic detritus, and small plants, as well as insects and other amphibian larvae. Tadpoles also feed on carrion and may even become cannibalistic, especially in breeding pools. Carnivorous larvae are able to grow and metamorphose faster due to the higher level of protein in their diet.

Animal Foods: amphibians; carrion ; insects; terrestrial non-insect arthropods

Plant Foods: algae; phytoplankton

Other Foods: detritus

Primary Diet: carnivore (Insectivore )

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Kadi, B. 2012. "Spea intermontana" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Spea_intermontana.html
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Bassel Kadi, University of Michigan-Ann Arbor
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Phil Myers, University of Michigan-Ann Arbor
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Rachelle Sterling, Special Projects
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Catherine Kent, Special Projects
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Associations

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Great Basin spadefoot toads affect populations of the arthropods they prey on. Due to the relative stability of their populations, the species also helps maintain the populations of its predators, as the toads are a relatively consistent source of food. They have no symbiotic or mutualistic interactions with any other species. Parasites that infect the species include Polystoma nearcticum in the lung and bladder, Distoichometra bufonis in the small intestine, Aplectana incerta in the small and large intestine, species of the genera Physaloptera (larvae) in the stomach, and Acuariidea (larvae) in cysts on the stomach wall.

Commensal/Parasitic Species:

  • lung and bladder parasites Polystoma nearcticum
  • intestinal parasites Distoichometra bufonis
  • intestinal parasites Aplectana incerta
  • stomach parasites Physaloptera (larvae)
  • stomach parasites Acuariidea (larvae)
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Kadi, B. 2012. "Spea intermontana" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Spea_intermontana.html
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Bassel Kadi, University of Michigan-Ann Arbor
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Phil Myers, University of Michigan-Ann Arbor
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Rachelle Sterling, Special Projects
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Catherine Kent, Special Projects
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Benefits

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There are no known positive impacts of Great Basin spadefoot toads on humans.

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Kadi, B. 2012. "Spea intermontana" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Spea_intermontana.html
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Bassel Kadi, University of Michigan-Ann Arbor
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Phil Myers, University of Michigan-Ann Arbor
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Rachelle Sterling, Special Projects
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Catherine Kent, Special Projects
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Benefits

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When threatened, adult Great Basin spadefoot toads can produce noxious skin secretions which may cause minor allergic reactions in humans, symptoms of which may include sneezing and a runny nose, and may also cause a burning sensation upon contact with the eyes and nose.

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Kadi, B. 2012. "Spea intermontana" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Spea_intermontana.html
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Bassel Kadi, University of Michigan-Ann Arbor
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Phil Myers, University of Michigan-Ann Arbor
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Rachelle Sterling, Special Projects
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Catherine Kent, Special Projects
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Life Cycle

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Eggs usually hatch within 2 to 4 days. Tadpoles transform in about 30 to 40 days, but the rate of metamorphosis can increase if the temporary pools in which the larvae are developing begin to dry out. Growth and differentiation rates are also influenced by temperature, which affects thyroid hormone activity (thyroid hormone is involved in metamorphosis). It is critical that larvae develop rapidly in species that breed in temporary pools, such as Spea intermontana, because metamorphosis must occur before the water evaporates, as the tadpoles cannot survive outside of water. Transformed juveniles still have a tail which disappears soon after they leave the breeding pools, and they may remain at the breeding location for a period of several days to several weeks before they leave the site. Transformed juveniles develop into sexually mature adults in 1 to 2 years for males, and in about 2 years for females.

Development - Life Cycle: metamorphosis

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Kadi, B. 2012. "Spea intermontana" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Spea_intermontana.html
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Bassel Kadi, University of Michigan-Ann Arbor
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Phil Myers, University of Michigan-Ann Arbor
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Rachelle Sterling, Special Projects
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Catherine Kent, Special Projects
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Behavior

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Males attract females to temporary breeding pools with loud calls while they are partially submerged in the water. These calls may also attract other males who will compete for the females. The calls are short, between 1 and 3 notes long, and duck-like. Because Spea intermontana is nocturnal, it has large eyes probably adapted to seeing at night. Great Basin spadefoot toads likely perceive their environment through a minimum of audio, visual, tactile and chemical stimuli.

Communication Channels: tactile ; acoustic ; chemical

Perception Channels: visual ; tactile ; acoustic ; chemical

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Kadi, B. 2012. "Spea intermontana" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Spea_intermontana.html
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Bassel Kadi, University of Michigan-Ann Arbor
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Phil Myers, University of Michigan-Ann Arbor
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Rachelle Sterling, Special Projects
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Catherine Kent, Special Projects
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Untitled

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Spea intermontana may sometimes be referred to as Spea intermontana.

Some studies place Spea intermontana as a sister group to to Spea bombifrons and suggest that S. intermontana is in fact paraphyletic.

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Kadi, B. 2012. "Spea intermontana" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Spea_intermontana.html
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Bassel Kadi, University of Michigan-Ann Arbor
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Phil Myers, University of Michigan-Ann Arbor
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Rachelle Sterling, Special Projects
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Catherine Kent, Special Projects
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Reproduction

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Great Basin spadefoot toads are explosive breeders, with all breeding completed in a few days. There is no specific or definite breeding season, but all breeding takes place from May through August, when temperature and water availability is favorable. There is much variation in the timing of mating each year due to the nature of mating locations. Adults are terrestrial, but breeding sites are located around water sources. As a result, adults of the species must migrate to the breeding sites. These journeys typically occur at night in order to limit exposure to dangers such as evaporative water loss and predation. The factors that stimulate mating are not very well understood. Rainfall may be one of them, but is not necessary for it as is the case with other spadefoot toad species. Adults migrate anywhere from 1 to 5 km to reach breeding sites.

The breeding pools may be permanent or temporary sources of water, such as rain-water pools, snowmelt, ponds, irrigation ditches, and streams. Breeding is more common in ephemeral water sources in areas where it rains enough to create temporary pools, and more common in permanent water sources in areas where it does not rain enough to create temporary pools. The water must be still or slow-moving to allow breeding. In order to support metamorphosis, breeding pools must remain filled for at least 40 days to allow enough time for eggs to hatch and for larval transformation.

Males migrate to breeding sites, partially submerge near the shore, and attempt to attract females using loud calls 1 to 3 notes in length. The calls, or choruses, are reported to be monotonous duck-like snoring sounds, and may be heard over great distances. The choruses attract females, and probably other males, to the breeding pools. As females arrive, males scramble and compete to find mates. Reproduction involves amplexus, where males embrace females from behind using their forelimbs. This position allows males to externally fertilize the female eggs as they emerge from the females' cloacae. When mating is completed, the adults quickly burrow underground to avoid evaporative water loss.

Mating System: polygynandrous (promiscuous)

After mating, females lay anywhere from 300 to 1000 eggs in small clusters of 10 to 40 eggs. They attach the egg clusters to floating sticks, submerged rocks, and underwater vegetation. Eggs usually hatch within 2 to 4 days, but may take longer if water temperatures are too cold. Their size at sexual maturity is unknown. Males mature sexually in the first 1 to 2 years after metamorphosis, while females do not sexually mature until at least the second year after metamorphosis.

Breeding interval: Great Basin spadefoot toads breed an average of once yearly if conditions are favorable.

Breeding season: Great Basin spadefoot toads will breed from May through August when conditions are favorable.

Range number of offspring: 300 to 1000.

Range time to hatching: 2 to 4 days.

Average age at sexual or reproductive maturity (female): 2 years.

Range age at sexual or reproductive maturity (male): 1 to 2 years.

Key Reproductive Features: iteroparous ; seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate); sexual ; fertilization (External ); oviparous

There is no parental involvement in the care for young once the eggs are laid. Females lay and attach their eggs to vegetation in bodies of water, and subsequently migrate back to feeding habitats, along with males, to replenish their energy reserves.

Parental Investment: no parental involvement; pre-fertilization (Provisioning, Protecting: Female)

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Kadi, B. 2012. "Spea intermontana" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Spea_intermontana.html
author
Bassel Kadi, University of Michigan-Ann Arbor
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Phil Myers, University of Michigan-Ann Arbor
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Rachelle Sterling, Special Projects
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Catherine Kent, Special Projects
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Associated Plant Communities

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More info for the term: shrub

Great Basin spadefoots occur in sagebrush (Artemisia spp.), shadscale
(Atriplex spp.), and other desert shrub types, plains grasslands, and
pinyon-juniper (Pinus-Juniperus spp.) woodlands [1,10]. In Utah and
northern Arizona, Great Basin spadefoots occur from low desert shrub
habitats up into spruce-fir (Picea-Abies spp.) forests [1].


A breeding pool in a desert wash community in Inyo County, California, that resulted from recent rains. Great Basin spadefoots were calling from the water and moving around the desert floor.
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Howard, Janet L. 1996. Spea intermontana. 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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Great Basin spadefoot
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Howard, Janet L. 1996. Spea intermontana. 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, natural, shrubs

Morphs and adult Great Basin spadefoots normally venture from their
burrows at night, when it is rainy or the night air is humid enough for
dew to collect [15]. Captive spadefoots (Scaphiopus spp.) have been
observed to dig shallow burrows in moist soil, then dig deeper (2 to 3
feet [0.7-1.2 m]) as soil dries at the surface. Spadefoots have been
found 15 feet (4.6 m) underground in natural conditions. An individual
spadefoot digs and occupies only one burrow, which it usually returns to
after foraging or mating. Darkness provides hiding security during
feeding; spadefoots do not use shrubs or other vegetation for cover
while foraging. Mating occurs in generally open water [3].
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Howard, Janet L. 1996. Spea intermontana. 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

provided by Fire Effects Information System Animals
The Great Basin spadefoot is distributed from south-central British
Columbia south to the eastern slope of the Sierra Nevada in California;
east to southern Nevada and northwestern Arizona; and northeast to
western Colorado and central Wyoming [7,18].
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Howard, Janet L. 1996. Spea intermontana. 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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More info for the term: cohort

Adult spadefoots are opportunistic carnivores. Adults hunt in spring
and summer, but only at night or during light rains. A variety of
species of insects, arachnids, and snails have been found in the
stomachs of adult spadefoots. Tadpoles feed on nearly every type of
water-borne organic matter: algae, rotting vegetation, bacteria- or
other humus-rich mud, insects, and the bodies of dead tadpoles.
Spadefoot tadpoles are dimorphic. Within a cohort, some tadpoles have
large mouthparts, while others have much smaller mouthparts. As well as
consuming other types of food, large-mouthed individuals are
cannibalistic, swallowing other tadpoles whole [3,20].
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bibliographic citation
Howard, Janet L. 1996. Spea intermontana. 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

provided by Fire Effects Information System Animals
More info for the term: cover

Research on the effects of fire on Great Basin spadefoots is lacking.
Habitat alteration by fire probably has no great impact on Great Basin
spadefoots, however. Great Basin spadefoots are not dependent upon
vegetation for cover. Fire would alter species composition of their
primarily arthropod prey base, but overall numbers of arthropod prey
would probably not change. Since Great Basin spadefoots are not
dependent upon any particular arthropod species as prey, they are
probably able to find food in the postfire environment.

Due to runoff, nutrient levels of breeding pools may increase after
fire, which could benefit tadpoles by encouraging growth of bacteria,
algae, and other tadpole foods. However, high levels of sediment, which
may wash into breeding pools as a result of postfire erosion, may
adversely impact tadpoles by reducing oxygen levels. Even if fire does
render breeding pools in a given basin inhospitable to tadpoles,
however, fire proabably has no serious impact on the Great Basin
spadefoot population of that basin. A large number of a tadpoles and
morphs in a Great Basin spadefoot population succumb to desiccation in
most breeding years, with population levels increasing greatly during
wet years [3,10]. Since most adults are probably unaffected by fire,
Great Basin spadefoot populations probably survive fire by the same
reproductive adaptations that enable them to survive drought.
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Howard, Janet L. 1996. Spea intermontana. 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):

206 Engelmann spruce-subalpine fir
208 Whitebark pine
216 Blue spruce
219 Limber pine
239 Pinyon-juniper
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Howard, Janet L. 1996. Spea intermontana. 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

FRES23 Fir-spruce
FRES26 Lodgepole pine
FRES29 Sagebrush
FRES30 Desert shrub
FRES35 Pinyon-juniper
FRES38 Plains grasslands
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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

K020 Spruce-fir-Douglas-fir forest
K022 Great Basin pine forest
K023 Juniper-pinyon woodland
K024 Juniper steppe woodland
K038 Great Basin sagebrush
K040 Saltbush-greasewood
K055 Sagebrush steppe
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Howard, Janet L. 1996. Spea intermontana. 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: Rangeland Cover Types

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This species is known to occur in association with the following Rangeland Cover Types (as classified by the Society for Range Management, SRM):

More info for the term: woodland

104 Antelope bitterbrush-bluebunch wheatgrass
105 Antelope bitterbrush-Idaho fescue
107 Western juniper/big sagebrush/bluebunch wheatgrass
210 Bitterbrush
314 Big sagebrush-bluebunch wheatgrass
315 Big sagebrush-Idaho fescue
316 Big sagebrush-rough fescue
317 Bitterbrush-bluebunch wheatgrass
318 Bitterbrush-Idaho fescue
319 Bitterbrush-rough fescue
320 Black sagebrush-bluebunch wheatgrass
321 Black sagebrush-Idaho fescue
324 Threetip sagebrush-Idaho fescue
401 Basin big sagebrush
402 Mountain big sagebrush
403 Wyoming big sagebrush
404 Threetip sagebrush
405 Black sagebrush
406 Low sagebrush
407 Stiff sagebrush
408 Other sagebrush types
412 Juniper-pinyon woodland
501 Saltbush-greasewood
504 Juniper-pinyon pine woodland
612 Sagebrush-grass
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Howard, Janet L. 1996. Spea intermontana. 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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Increased irrigation and range improvements in the Great Basin have
benefitted the Great Basin spadefoot [15]. Hovingh and others [10]
noted that on their Bonneville Basin study area, only 8 percent of
breeding waters utilized by Great Basin spadefoots were entirely
natural. Populations have declined where water has been diverted,
however.
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Howard, Janet L. 1996. Spea intermontana. 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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AZ
CA
CO
ID
NV
OR
UT
WA
WY

BC

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Howard, Janet L. 1996. Spea intermontana. 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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Mud turtles (Kinosternon flavescens), spotted skunks (Spilogale
putarius) [13], raccoons (Procyon lotor) [5], common crows (Corvus
brachyrhynchos), and other tadpoles [9] have been noted to prey upon
spadefoot tadpoles. Many other animal species probably prey on both
tadpole and morph Great Basin spadefoots. Predators of adult Great
Basin spadefoots have not been described in current literature, although
predation of adults is thought to occur [10]. Predation is probably
reduced by the primarily nocturnal habit of adults [3]. In addition,
adult Great Basin spadefoots secrete an odorous, skin-burning mucous
from the paratoid glands when bitten or handled; they may also
regurgitate when bitten or handled. Many predators are probably
deterred by these traits [19].
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Howard, Janet L. 1996. Spea intermontana. 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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More info for the terms: cover, grassland

Great Basin spadefoots occupy cold desert and arid grassland habitats at
low to high elevations. Great Basin spadefoots have been found at 8,500
feet (2,600 m) elevation in Wyoming [3]. Morph and adult Great Basin
spadefoots live in burrows. They dig the burrows with their
spade-shaped hindfeet, then cover the burrow entrance with soil. The
only time they normally emerge from their burrows is when air is moist
[3].

Breeding occurs in spring runoff pools, reservoirs, permanent and
temporary springs, irrigation ditches, and basin lakes [10]. During
their short tadpole life stage, Great Basin spadefoots live in these
breeding waters [3,4]. Great Basin spadefoots usually do not utilize
strongly alkaline water: Hovingh and others [10] found that most
breeding waters contained less than 1,000 mg/L of dissolved solids.
Breeding sites often have greatly fluctuating volumes of water that
evaporate by autumn. In the Bonneville Basin, breeding pools with
adundant vegetation showed less tadpole recruitment than pools with
sparse vegetative growth. The most successful breeding sites were
streambeds scoured by flash floods, reservoirs that had large draw-downs
of water (and thus lacked a littoral zone of vegetation), and temporary
waters that dried by autumn [10].
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Howard, Janet L. 1996. Spea intermontana. 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):

5 Columbia Plateau
6 Upper Basin and Range
7 Lower Basin and Range
10 Wyoming Basin
12 Colorado Plateau
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Howard, Janet L. 1996. Spea intermontana. 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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Scaphiopus intermontanus Cope [2,7,18]
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Howard, Janet L. 1996. Spea intermontana. 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 scientific name of Great Basin spadefoot is Spea intermontana
(Cope) (Pelobatidae) [21,22].
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Howard, Janet L. 1996. Spea intermontana. 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 term: cover

Breeding: Great Basin spadefoots breed in spring and early summer.
Hovingh and others [10] reported that in the Bonneville Basin of Utah,
breeding occurred from April to mid-June. Breeding after early summer
is probably uncommon. Spring rains usually provide the stimulus for
males to emerge from their burrows for breeding, although unlike other
spadefoots (Scaphiopus spp.), Great Basin spadefoots do breed during
periods of no rainfall. The stimulus for emergence for breeding in the
absence of rain is unknown. Males move to breeding waters first and
begin vocalizing. Female Great Basin spadefoots move to breeding waters
after only a few males are vocalizing [10].

Each female produces several hundred eggs contained in a sticky gel.
The female deposits her fertilized eggs in several different locations
within the breeding water: on vegetation, rocks, or anything else that
anchors the eggs. After mating, females return to their burrows.
Males stay at the breeding pool and continue vocalizing until females
stop arriving (presumably because all females in the vicinity have
mated); then the males also return to their burrows [3].

 

Mature egg and tadpole stages of development. Photos by Gary Nafis.

Development: Developing rapidly helps Great Basin spadefoots avoid
desiccation and consequent death in their arid environment. Great Basin
spadefoot eggs probably hatch within 2 to 3 days of deposition [15].
Tadpole development and metamorphosis is complete within 4 to 8 weeks,
depending upon temperature, food quality, and food quantity. Brown [4]
found that recently fertilized Great Basin spadefoot egg masses,
collected on 20 May from a temporary pond in eastern Washington and
placed in an aquarium, hatched a day later. Hindlegs of tadpoles in the
aquarium developed by 18 days of age, and forelimbs developed by 31
days. Tadpole body mass was greatest at 33 days, when complete head
reorganization (eyes, ears, jaws, muscles, and gill absorption) was
complete. Tail length was greatest 30 days after hatching; the tail was
reabsorped 40 days after hatching [4]. In the wild, temporary waters
frequently dry out and tadpoles die before larval development is
complete [3,4]. Rate of tadpole development may vary with breeding pool
type. In Texas, tadpoles of a related species, Couch's spadefoot
(Scaphiopus couchii), were found to develop more slowly in permanent
waters than in temporary ponds [14].

Young morphs (metamorphosed preadults) are small; Nussbaum and others
[15] reported that recently metamorphosed Great Basin spadefoots in
north-central Oregon averaged 0.8 inch (19 mm) in length [16]. (Adults
are from 1.5 to 2.5 inches [3.7-6.4 cm] long [18].) Great Basin
spadefoots have high surface-to-volume ratios as morphs. Consequently,
they are highly susceptible to desiccation and seek shade cover
immediately after emerging from breeding pools. Young spadefoots grow
rapidly. Under laboratory conditions, Couch's spadefoot morphs showed a
110 percent increase in length and over a 1,100 percent increase in mass
in a 3-month period [16].

Hibernation: Spadefoots accumulate fat rapidly in summer. They are
dormant in fall and winter, with dormancy and apparently triggered by
photoperiod [16]. Spring emergence may be triggered by increased
moisture in the burrow [3].

Spadefoots extend their dormancy period during drought, and can
apparently remain dormant or mostly dormant for long periods of time.
Fat reserves are metabolized slowly during dormancy, and females may
reabsorb their eggs if spring rains do not occur. Mayhew [12]
speculated that Couch's spadefoots in the extremely arid Imperial Valley,
California, survived a 20-year local drought by remaining dormant except
during rare summer thunderstorms.
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Howard, Janet L. 1996. Spea intermontana. 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 term: fire regime

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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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Howard, Janet L. 1996. Spea intermontana. 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/

Great Basin spadefoot

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The Great Basin spadefoot (Spea intermontana) is an amphibian in the family Scaphiopodidae. It is 3.8 to 6.3 centimetres (1.5 to 2.5 in) long and is usually colored gray, olive or brown. Great Basin spadefoot toads have adapted to life in dry habitats. They use the hard, keratinized spade on each foot to dig a burrow, where they spend long periods during cold and dry weather. They are opportunistic hunters and will eat anything they can subdue. While their tadpoles have numerous predators, adults are able to produce skin secretions that deter enemies.

Identification

The Great Basin spadefoot ranges from 3.8 to 6.3 centimetres (1.5 to 2.5 in) long.[3] It is usually gray, olive or brown colored. Gray streaks outline an hourglass-shaped marking on the back. The skin is smooth compared with the bumpy skin of the true toads in the genus Bufo. There is a spade present on the inside of each hind foot; it has sharp edges and is wedge-shaped. A glandular boss is present between the eyes. Eyes are catlike; pupils are vertical in bright light and round at night. Dark brown spots are present on each upper eyelid.

Habitat and distribution

The natural habitats of the Great Basin spadefoot include pinyon-juniper, ponderosa pine, and high elevation (up to 2,600 metres or 8,500 feet[4]) spruce-fir forests, semidesert shrubland, sagebrush flats, temperate grasslands, and deserts. They are present in agricultural areas as well. The Great Basin Spadefoot can be found from southern British Columbia through the eastern portions of Washington and Oregon and in southern Idaho. Their range extends throughout all of Nevada and into most of Utah; they are also present in small areas in California, Arizona, Colorado, and Wyoming.[3][5]

Reproduction

Breeding

Breeding is explosive, meaning that large congregations of individuals assemble and mate with each other. Adults are terrestrial and must migrate to breeding sites. Breeding may take place in permanent or temporary water sources such as springs, sluggish streams, and manmade reservoirs during the months of April through July. Spring rains usually provide the stimulus for males to emerge from their burrows for breeding, although unlike other spadefoots (Scaphiopus spp.), Great Basin spadefoots do breed during periods of no rainfall. The stimulus for breeding in the absence of rain is unknown. Males move to breeding waters first and begin vocalizing.[6] Once females arrive, there is a race to mate with as many others as possible, and physical contests between males are common.

Females usually lay 300–500 eggs contained in a sticky gel, but have been reported lay as many as 1000 eggs in captivity. The female deposits her fertilized eggs in several different locations within the breeding water: on vegetation, rocks, bottom of the pool, or anything else that anchors the eggs. After mating, females return to their burrows. Males stay at the breeding pool and continue vocalizing until females stop arriving (presumably because all females in the vicinity have mated); then the males also return to their burrows.[4]

Development

Eggs hatch in 2 to 4 days,[7] and the tadpole development and metamorphosis is complete within 4 to 8 weeks, depending upon temperature, food quality, and food quantity. Developing rapidly helps Great Basin spadefoots avoid desiccation and consequent death in their arid environment.[4]

Young morphs (metamorphosed preadults) are small, about 0.8 inch (19 mm) in length on average.[7][8] They have high surface-to-volume ratios; therefore, they are highly susceptible to desiccation and seek shade cover immediately after emerging from breeding pools. They grow, by about 110% in length and 1,100% in mass over 3 months under laboratory conditions.[8] Tadpoles may be carnivorous or herbivorous, depending on environmental conditions. Different larval diets are associated with different morphological characteristics.[9]

Behavior

Diet

Adult spadefoots are opportunistic carnivores. Adults have been shown to eat arthropods from the taxa Coleoptera, Diptera, Hemiptera, Hymenoptera, Lepidoptera, Neuroptera, Orthoptera, Trichoptera, Collembola, and Araneae. Ants and beetles are their most common prey. Feeding seems to be generalized and opportunistic; the toads will eat anything they can subdue.[4]

Adults hunt in spring and summer, but only at night or during light rains. Spadefoot tadpoles are dimorphic. Within a cohort, some tadpoles have large mouthparts, while others have much smaller mouthparts. As well as consuming other types of food, large-mouthed individuals are cannibalistic, swallowing other tadpoles whole.[4][10]

Defense mechanisms

Reported predators of adult Great Basin spadefoot toads include rattlesnakes, coyotes, and owls. Predators of larva include mud turtles (Kinosternon flavescens), spotted skunks (Spilogale putarius),[11] raccoons (Procyon lotor),[12] common crows (Corvus brachyrhynchos) and snakes. Adults are able to produce skin secretions that cause allergic reactions in some humans, including a burning sensation if the secretion gets in the eyes or nose. The skin secretions also deter predators.[13]

Burrowing behavior

Great Basin spadefoot toads have adapted to life in dry habitats. Desiccation is avoided by this terrestrial amphibian through burrowing into the ground. The toad use the hard, keratinized spade on each foot to dig a burrow, where it spends long periods during cold and dry weather. The toad is able to absorb water from the surrounding soil; even as the soil becomes increasingly dry in spring and early summer months, increased concentrations of urea in the toad's body allow it to continue to suck water out of the soil through osmosis. When the summer rains arrive the Great Basin spadefoot emerges from its burrow.[4]

Morphs and adult Great Basin spadefoots normally venture from their burrows at night, when it is rainy or the night air is humid enough for dew to collect.[7] Captive spadefoots have been observed to dig shallow burrows in moist soil, then dig deeper (2 to 3 feet [0.7–1.2 m]) as soil dries at the surface. Spadefoots have been found 15 feet (4.6 m) underground in natural conditions. An individual spadefoot digs and occupies only one burrow, which it usually returns to after foraging or mating. Spadefoots do not use shrubs or other vegetation for cover while foraging.[4]

Spadefoots accumulate fat rapidly in summer. They are dormant in fall and winter, with dormancy apparently triggered by photoperiod.[8] Spring emergence may be triggered by increased moisture in the burrow.[4] Spadefoots extend their dormancy period during drought, and can apparently remain dormant or mostly dormant for long periods of time. Fat reserves are metabolized slowly during dormancy, and females may reabsorb their eggs if spring rains do not occur.[9]

References

Public Domain This article incorporates public domain material from Scaphiopus intermontanus. United States Forest Service.

  1. ^ IUCN SSC Amphibian Specialist Group (2022). "Spea intermontana". IUCN Red List of Threatened Species. 2022: e.T59046A196337412. doi:10.2305/IUCN.UK.2022-1.RLTS.T59046A196337412.en. Retrieved 12 May 2023.
  2. ^ "Spea intermontana (Cope, 1883)". Integrated Taxonomic Information System. Retrieved 12 May 2023.
  3. ^ a b Stebbins, Robert C. 1985. Western reptiles and amphibians. 2nd ed. Peterson Field Guides No. 16. Boston: Houghton Mifflin Company.
  4. ^ a b c d e f g h Bragg, Arthur N. (1965). Gnomes of the night. Philadelphia: University of Pennsylvania Press
  5. ^ Frost, Darrel R. (ed.) 1985. Amphibian species of the world: a taxonomic and geographic reference. Lawrence, KS: Allen Press, Inc. ISBN 0942924118
  6. ^ Hovingh, Peter; Benton, Bob; Bornholdt, Dave (1985). "Aquatic parameters and life history observations of the Great Basin spadefoot toad in Utah". Great Basin Naturalist. 45 (1): 22–30. doi:10.5962/bhl.part.4431.
  7. ^ a b c Nussbaum, Ronald A.; Brodie, Edmund D., Jr.; Storm, Robert M. (1983). Amphibians and reptiles of the Pacific Northwest. Northwest Naturalist Books. Moscow, ID: University of Idaho Press ISBN 0893010863
  8. ^ a b c Seymour, Roger S. (1973). "Energy metabolism of dormant spadefoot toads (Scaphiopus)". Copeia. 3 (3): 435–445. doi:10.2307/1443107. JSTOR 1443107.
  9. ^ a b Scaphiopus intermontanus. United States Forest Service. fs.fed.us
  10. ^ Whitaker, John O., Jr.; Rubin, David; Munsee, Jack R. (1977). "Observations on food habits of four species of spadefoot toads, genus Scaphiopus". Herpetologica. 33 (4): 468–475. JSTOR 3891718.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  11. ^ Newman, R. A. (1987). "Effects of density and predation on Scaphiopus couchi tadpoles in desert ponds". Oecologia. 71 (2): 301–307. Bibcode:1987Oecol..71..301N. doi:10.1007/BF00377299. PMID 28312260. S2CID 19861570.
  12. ^ Childs, Henry E., Jr. (1953). "Selection by predation on albino and normal spadefoot toads". Evolution. 7 (3): 228–233. doi:10.2307/2405733. JSTOR 2405733.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  13. ^ Waye, Heather L.; Shewchuk, Christopher H. (1995). "Scaphiopus intermontanus (Great Basin spadefoot). Production of odor". Herpetological Review. 26 (2): 98–99.
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Great Basin spadefoot: Brief Summary

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The Great Basin spadefoot (Spea intermontana) is an amphibian in the family Scaphiopodidae. It is 3.8 to 6.3 centimetres (1.5 to 2.5 in) long and is usually colored gray, olive or brown. Great Basin spadefoot toads have adapted to life in dry habitats. They use the hard, keratinized spade on each foot to dig a burrow, where they spend long periods during cold and dry weather. They are opportunistic hunters and will eat anything they can subdue. While their tadpoles have numerous predators, adults are able to produce skin secretions that deter enemies.

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