Boreal chorus frog

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Boreal chorus frog
Pseudacris maculata.jpg
Scientific classification Red Pencil Icon.png
Kingdom: Animalia
Phylum: Chordata
Class: Amphibia
Order: Anura
Family: Hylidae
Genus: Pseudacris
Species:
P. maculata
Binomial name
Pseudacris maculata
Agassiz, 1850
Pseudacris maculata map.svg
Range of P. maculata

The boreal chorus frog (Pseudacris maculata) is a species of chorus frog native to Canada from central Quebec to eastern British Columbia and north to the Northwest Territories and the southern portion of the Yukon. [2] It occurs in the USA throughout Montana, northwestern Wisconsin, northeastern Arizona, northern New Mexico, and southwestern Utah.

Contents

Description

This small species of frog reaches about 30 mm in length. It is highly variable, but is normally brown, and can be green on the dorsal surface, with three broken dorsal stripes; these stripes can be very distinct to quite faint. A dark band is present from the snout, across the eye, and continuing down the side. It has slightly enlarged toe pads to help in climbing small grasses and vegetation. This species is very similar to the western chorus frog (Pseudacris triseriata). It can be distinguished from this species by having shorter legs.

Ecology and behaviour

This species can be found around permanent water bodies in cleared land and forest. Males make a "reeeek" call from grasses, vegetation, or ground around the water body from April through to September. This call is characteristic of the trilling frog clade that is present in the genus Pseudacris. This clade is so named because the call of each individual is different, each having its own series of pulses. [2] Within the trilling frog clade, they are further divided into "dynamic" and "static" groups, and recent studies have placed P. maculata into the static grouping. The static grouping is distinguished by a lack of variability in one's call and the ability to somewhat control the direction of their calls. [2] Amphibians' songs or calls to one another are commonly used for sexual selection, but in Bee, et al. 2010, the researchers found no correlation that linked directly to sexual selection. They found a link between the lowest note in the song and body size, but insufficient evidence to draw any conclusions from it. Every call was different in the study, but the differences were subtle and required complex technology to pick up. The similarity in the calls results in the frogs not being able to distinguish individuals from each other. It was hypothesized that the calls were simply to broadcast their position to other calling males telling them to stay away and also to alert females to the presence of a male that is ready to mate. [2] This is normally one of the first species of amphibian to emerge in spring. It comes out so early that it is often found while snow and ice are still present. This timing directly correlates with snow-melt and the water level of the water body that the populations calls home. [3]

Pseudacris maculata is categorized as an annual breeder. [4] Breeding takes place once the weather begins to warm, typically from late February to around April. [4] After mating, a single female can lay anywhere from 500-1500 eggs, with a highly variable hatching rate of anywhere from 37% to 87%.The life cycle continues with tadpoles metamorphosing around June or July. [4] The metamorphosis survival rate also has a massive range of 10-100% in the wild. [4]

Threats

Amphibians are widely known as very important species in their ecosystems, but declines are occurring worldwide in amphibian populations. There are multiple reasons that amphibians decline, with the most common being disease, habitat loss, over harvesting for food, pet trade, and competition with invasive species. Climate change has also been one of the proposed mechanisms for why this species is struggling . [5] Climate change is causing the weather to become increasingly dry, which affects most amphibians (including Pseudacris maculata). This change leads them to modify their behavior based on the environmental conditions and sometimes exposing them to conditions that are not optimal. [5] This dry weather has another effect on this species, it results in lower water levels, which exposes the amphibians and their eggs (which are laid in the water) to more extreme temperatures. This, coupled with the decrease in ozone layers, also exposes the amphibians and the eggs to heightened levels of UV radiation when compared to environments with deeper waters. [3]

The boreal chorus frog has an interesting defense to invasive species. This species of frog has been found to have cultural learning on how to behave towards predators. Cultural learning is learning that takes place by an individual observing and imitating behaviors of other individuals in close proximity. The example brought up by Ferrari and Chivers 2008, is how P. maculata tadpoles learn to avoid salamanders from tadpoles that have experience with the predator. The paper discusses how if a new predator is added to the environment, there is a learning curve at how long it takes the tadpoles to learn to avoid the new predator. [6] The addition of an invasive species will be very successful until the tadpoles learn to avoid it, which could cause even more pressure on this species.

Amphibians worldwide are being infected with the fungus Batrachochytrium dendrobatidis (Bd) and the boreal chorus frog is no exception. Bd infects the keratinized skin of its host, which results in an inability to properly osmoregulate through the skin. The symptoms to this disease vary between species, ranging from seemingly unaffected to death. [4] This species of frog has been found to be infected at higher frequencies than other amphibians in the same environments. [7] There have been many studies examining how this species copes with an infection of Bd. Some studies claim that Pseudacris maculata is struggling (8), [8] while others show that populations are maintaining themselves. [4] This is especially intriguing when one considers that the boreal chorus frog can have mortality up to 80% when infected with Bd. [4] No definitive conclusions can be drawn with how Pseudacris maculata copes with the disease within a population.

Bd is an especially interesting and dangerous pathogen given the fact that it can persist in an environment even in the absence of amphibians. [9] It can survive in water for an extended amount of time, as well as attach to feathers. [9] These facts, on top of the fact that Bd can also infect salamanders and frogs in all stages of life result in the pathogen persisting in an environment long enough to continually infect new frogs (9,11). [10] Tadpoles can be infected on their mouth parts (which is the only location of keratinized skin) and frogs post-metamorphosis can be infected almost anywhere (but primarily on the toes). [4] The significance that salamanders (specifically tiger salamanders from the paper) can be infected is because they can perpetuate the presence of Bd in the environment which can then increase the odds that a frog will be infected by this disease. Salamanders can also overwinter in the water itself, while frogs live terrestrially during the winter. This is significant because without the living hosts keeping Bd alive in the water, it would have a high chance to die off over the winter in the water with no hosts. [4] Boreal chorus frogs in areas that contain salamanders capable of surviving with Bd cannot escape this disease, which could be why some populations are declining.

Related Research Articles

Amphibian Class of ectothermic tetrapods

Amphibians are ectothermic, tetrapod vertebrates of the class Amphibia. All living amphibians belong to the group Lissamphibia. They inhabit a wide variety of habitats, with most species living within terrestrial, fossorial, arboreal or freshwater aquatic ecosystems. Thus amphibians typically start out as larvae living in water, but some species have developed behavioural adaptations to bypass this.

Tiger salamander Species of amphibian

The tiger salamander is a species of mole salamander and one of the largest terrestrial salamanders in North America.

Decline in amphibian populations Ongoing mass extinction of amphibian species worldwide

Since the 1980s, decreases in amphibian populations, including population decline and localized mass extinctions, have been observed in locations all over the world. These declines are known as one of the most critical threats to global biodiversity.

Chytridiomycosis

Chytridiomycosis(chy·​trid·​i·​o·​my·​co·​sis | \ kī-ˌtri-dē-ō-mī-ˈkō-səs) is an infectious disease in amphibians, caused by the chytrid fungi Batrachochytrium dendrobatidis and Batrachochytrium salamandrivorans, a non-hyphal zoosporic fungus. Chytridiomycosis has been linked to dramatic population declines or extinctions of amphibian species in western North America, Central America, South America, eastern Australia, East Africa (Tanzania), and Dominica and Montserrat in the Caribbean. Much of the New World is also at risk of the disease arriving within the coming years. The fungus is capable of causing sporadic deaths in some amphibian populations and 100% mortality in others. No effective measure is known for control of the disease in wild populations. Various clinical signs are seen by individuals affected by the disease. A number of options are possible for controlling this disease-causing fungus, though none has proved to be feasible on a large scale. The disease has been proposed as a contributing factor to a global decline in amphibian populations that apparently has affected about 30% of the amphibian species of the world. Some research found evidence insufficient for linking chytrid fungi and chytridiomycosis to global amphibian declines, but more recent research establishes a connection and attributes the spread of the disease to its transmission through international trade routes into native ecosystems.

Pacific tree frog Species of amphibian

The Pacific tree frog, also known as the Pacific chorus frog, has a range spanning the Pacific Northwest, from Northern California, Oregon, and Washington to British Columbia in Canada and extreme southern Alaska. They live from sea level to more than 10,000 feet in many types of habitats, reproducing in aquatic settings. They occur in shades of greens or browns and can change colors over periods of hours and weeks.

Mountain yellow-legged frog Species of amphibian

The mountain yellow-legged frog, also known as the southern mountain yellow-legged frog, is a species of true frog endemic to California in the United States. It occurs in the San Jacinto Mountains, San Bernardino Mountains, and San Gabriel Mountains in Southern California and the Southern Sierra Nevada. It is a federally listed endangered species.

Boreal toad Subspecies of amphibian

The boreal toad is the nominate subspecies of the western toad. They are commonly found in the Southern Rocky Mountains, and their population has recently been on the decline due to an emerging amphibian disease, chytrid fungus. The boreal toad is currently listed as an endangered species by Colorado and New Mexico. It is known in Colorado as the only alpine species of toad.

<i>Batrachochytrium dendrobatidis</i> Species of fungus

Batrachochytrium dendrobatidis, also known as Bd or the amphibian chytrid fungus, is a fungus that causes the disease chytridiomycosis in amphibians.

Western chorus frog Species of amphibian

The western chorus frog, also known as striped chorus frog, or midland chorus frog is a species of frog found in Canada and the United States.

Panamanian golden frog Species of amphibian

The Panamanian golden frog, also known as Cerro Campana stubfoot toad and other names, is a species of toad endemic to Panama. Panamanian golden frogs inhabit the streams along the mountainous slopes of the Cordilleran cloud forests of west-central Panama. While the IUCN lists it as critically endangered, it may in fact have been extinct in the wild since 2007. Individuals have been collected for breeding in captivity in a bid to preserve the species. The alternative common name, Zetek's golden frog, and the epithet zeteki both commemorate the entomologist James Zetek.

The Copan brook frog is a species of frog in the family Hylidae found in northeastern Guatemala and northwestern Honduras, specifically in the Sierra del Merendón, Sierra de Omoa, Sierra de Caral, and Sierra Espíritu Santo ranges. The colouring of this species is very distinctive and the specific name soralia comes from the resemblance of its markings to the vegetative structures on some crustose lichens.

<i>Agalychnis lemur</i> Species of amphibian

Agalychnis lemur, also known as the lemur leaf frog or lemur frog, is a species of frog in the family Phyllomedusidae, also treated as the subfamily Phyllomedusinae in the Hylidae. It is found in Costa Rica, Panama, and adjacent northwestern Colombia. It is classed as Critically Endangered and threatened by the fungal disease chytridiomycosis.

Green-eyed treefrog Species of amphibian

The green-eyed treefrog is a species of Australasian treefrog in the family Pelodryadidae that occurs in the Wet Tropics of Australia.

Chile Darwins frog Species of amphibian

The Chile Darwin's frog, also called the northern Darwin's frog, is one of only two members of the family Rhinodermatidae. It is endemic to central Chile, although it might well be extinct.

<i>Janthinobacterium lividum</i> Species of bacterium

Janthinobacterium lividum is an aerobic, Gram-negative, soil-dwelling bacterium that has a distinctive dark-violet color, due to a compound called violacein, which is produced when glycerol is metabolized as a carbon source. Violacein has antibacterial, antiviral, and antifungal properties. Its antifungal properties are of particular interest, since J. lividum is found on the skin of certain amphibians, including the red-backed salamander, where it prevents infection by the devastating chytrid fungus.

Golden toad Extinct species of toad that was endemic to Costa Rica

The golden toad is an extinct species of true toad that was once abundant in a small, high-altitude region of about 4 square kilometres (1.5 sq mi) in an area north of the city of Monteverde, Costa Rica. It was endemic to elfin cloud forest. Also called the Monte Verde toad, Alajuela toad and orange toad, it is commonly considered the "poster child" for the amphibian decline crisis. This toad was first described in 1966 by herpetologist Jay Savage. The last sighting of a single male golden toad was on 15 May 1989, and it has since been classified as extinct by the International Union for Conservation of Nature (IUCN).

<i>Ecnomiohyla rabborum</i> Species of frog in the family Hylidae

Ecnomiohyla rabborum, commonly known as Rabbs' fringe-limbed treefrog, is a possibly extinct species of frog in the family Hylidae. They were relatively large frogs that inhabited the forest canopies of central Panama. Like other members of the genus Ecnomiohyla, they were capable of gliding by spreading their enormous and fully webbed hands and feet during descent. The males of the species were highly territorial and would guard water-filled tree holes used for breeding. They were also the ones responsible for guarding and caring for the young, including providing food. They were the only known species of frog where the tadpoles derived nutrition by feeding on the skin cells of their fathers.

<i>Batrachochytrium salamandrivorans</i> Species of pathogenic chytrid fungus that infects amphibian species

Batrachochytrium salamandrivorans (Bsal) is a pathogenic chytrid fungus that infects amphibian species. Although salamanders and newts seem to be the most susceptible, some anuran species are also affected. Bsal has emerged recently and poses a major threat to species in Europe and North America.

<i>Telmatobius ventriflavum</i> Species of amphibian

Telmatobius ventriflavum, the Andean Water Frog, is a species of water frogs from the western Andes in Peru.

Karen Lips US herpetologist

Karen R. Lips is a Professor of Biology at University of Maryland, College Park. Lips' work in the 1990s eventually contributed to the identification of the chytrid fungus as the primary cause of frog decline worldwide.

References

  1. IUCN SSC Amphibian Specialist Group (2015). "Pseudacris maculata". IUCN Red List of Threatened Species . 2015: e.T136004A78906835. doi: 10.2305/IUCN.UK.2015-4.RLTS.T136004A78906835.en . Retrieved November 12, 2021.
  2. 1 2 3 4 Bee, M. A., Cook, J. M., Love, E. K., O'Bryan, L. R., Pettitt, B. A., Schrode, K. and Vélez, A. (2010). "Assessing Acoustic Signal Variability and the Potential for Sexual Selection and Social Recognition in Boreal Chorus Frogs (Pseudacris maculata)." Ethology 116: 564–576. doi:10.1111/j.1439-0310.2010.01773.x
  3. 1 2 Corn, Paul Stephen, and Erin Muths (2002). "Variable breeding phenology affects the exposure of amphibian embryos to ultraviolet radiation." Ecology 83(11): 2958-2963.
  4. 1 2 3 4 5 6 7 8 9 Hyman, Oliver (2012). Ecology of Chytridiomycosis in Boreal Chorus Frogs (Pseudacris maculata). Diss. Arizona State University.
  5. 1 2 Amburgey, Staci, et al. (2012). "Effects of hydroperiod duration on survival, developmental rate, and size at metamorphosis in boreal chorus frog tadpoles (Pseudacris maculata)." Herpetologica 68(4): 456-467.
  6. Ferrari, Maud CO, and Douglas P. Chivers (2008). "Cultural learning of predator recognition in mixed-species assemblages of frogs: the effect of tutor-to-observer ratio." Animal Behaviour 75(6): 1921-1925.
  7. 7. Rodriguez, Edmarie Martinez et al. (2009). "Presence of Batrachochytrium Dendrobatidis at the Headwaters of the Mississippi River, Itasca State Park, Minnesota, USA." Herpetological Review 40(1): 48–50. Print.
  8. Seburn, David C., Kari Gunson, and Frederick W. Schueler (2014). "Apparent widespread decline of the Boreal Chorus Frog (Pseudacris maculata) in eastern Ottawa." The Canadian Field-Naturalist 128(2): 151-157.
  9. 1 2 Wixson, Joel G., and Kevin B. Rogers (2009). "Detecting Batrachochytrium dendrobatidis in the wild when amphibians are absent." Herpetological Review 40(3): 313.
  10. Davidson, Elizabeth W., et al. (2003). "Pathogenicity and transmission of chytridiomycosis in tiger salamanders (Ambystoma tigrinum)." Copeia 2003(3): 601-607.