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Cope's gray treefrog

Cope's gray treefrog (Dryophytes chrysoscelis) is a medium-sized arboreal hylid frog native to the eastern United States and parts of southeastern Canada, distinguished from its close relative the gray treefrog (D. versicolor) primarily by its diploid chromosome number and faster mating call trill.^[1]^[2] Adults typically measure 3.2–5.1 cm (1.25–2 inches) in snout-vent length, with granular skin, large adhesive toe pads for climbing, and variable coloration ranging from mottled gray to light green, often featuring a bright yellow to orange flash on the inner thighs and a pale spot beneath the eye.^[3]^[4] This nocturnal species inhabits mature deciduous forests and woodland edges, where it forages on small invertebrates like insects and spiders, hiding in tree cavities or under bark during the day.^[3]^[5] Breeding occurs from late April to August in fishless temporary wetlands such as vernal pools, roadside ditches, and woodland ponds, with males producing a rapid, buzz-like trill to attract females; eggs are laid in surface films on vegetation, hatching into tadpoles that develop over about two months.^[2]^[3] The range of D. chrysoscelis spans much of the eastern United States, from central Texas and northern Florida northward to southeastern Canada, including states like Illinois, Kansas, Kentucky, and Georgia, though it is absent from peninsular Florida and less common in some northern areas where it coexists with D. versicolor.^[6]^[3]^[7] It thrives in forested habitats but shows tolerance for human-modified edges, such as oak savannas and areas near houses where it may be attracted to lights for prey.^[8]^[5] A notable adaptation is its freeze tolerance, allowing survival of extracellular freezing of up to 65% of body water during winter hibernation, facilitated by a cryoprotectant system involving rapid mobilization of glycerol (increasing 370-fold in plasma during freezing), glucose from hepatic glycogen, and elevated urea levels.^[9] This species produces mild skin toxins that can irritate mucous membranes, providing defense against predators, and its cryptic similarity to D. versicolor often requires genetic or acoustic analysis for identification.^[3]^[2] Overall, D. chrysoscelis plays a key role in forest ecosystems as both predator and prey, with populations generally stable but potentially vulnerable to habitat loss and climate shifts affecting breeding sites.^[6]^[3]

Taxonomy

Classification

Cope's gray treefrog is classified in the order Anura, family Hylidae, genus Dryophytes, and species D. chrysoscelis (formerly Hyla chrysoscelis).^[10] The species was first described as Hyla chrysoscelis by American herpetologist Edward Drinker Cope in 1880, based on specimens from the southeastern United States.^[11] The specific epithet chrysoscelis originates from the Greek words chrysos (gold) and skelos (leg), referring to the conspicuous yellow-orange flash colors on the hidden surfaces of the hind legs.^[4] Phylogenetic studies in 2016 led to a taxonomic revision of Hylidae, resurrecting the genus Dryophytes Fitzinger, 1843, for North American and East Asian treefrogs previously in Hyla, including D. chrysoscelis, to better reflect evolutionary relationships.^[12] This classification is accepted by authorities such as AmphibiaWeb and Amphibian Species of the World but remains controversial and is not followed by the Society for the Study of Amphibians and Reptiles (SSAR) as of 2025.^[13] This species forms a cryptic complex with the gray treefrog (Dryophytes versicolor), differing mainly in chromosome number and advertisement calls.^[10]

Genetic distinction

Cope's gray treefrog (Dryophytes chrysoscelis) is genetically distinguished from the morphologically similar northern gray treefrog (Dryophytes versicolor) primarily by its diploid chromosome number of 2n=24, in contrast to the tetraploid 4n=48 chromosomes of D. versicolor.^[14]^[15] This ploidy difference arose through whole-genome duplication in the lineage leading to D. versicolor, which recent genomic analyses suggest occurred approximately 100,000 years ago from an extinct northeastern population of D. chrysoscelis, marking a key speciation event via autopolyploidy.^[16]^[17] Although the two species exhibit high genetic similarity, with subgenomes of D. versicolor showing less than 0.5% pairwise distance from D. chrysoscelis, rare hybridization occurs in zones of sympatry, resulting in triploid offspring (3n) that typically exhibit reduced fertility or sterility due to the ploidy mismatch.^[16]^[18] This reproductive barrier reinforces genetic isolation, with gene flow primarily unidirectional from the diploid D. chrysoscelis to the tetraploid D. versicolor.^[19]^[20] Confirmation of species identity beyond advertisement calls relies on cytogenetic and molecular methods, including direct chromosome counts to verify ploidy and DNA sequencing of nuclear loci or mitochondrial genomes to detect lineage-specific markers.^[14]^[17] Tools such as anchored hybrid enrichment, which targets hundreds of loci, or software like nQuire for ploidy estimation, provide robust discrimination in research settings.^[16]^[15]

Physical description

Morphology

Cope's gray treefrog (Dryophytes chrysoscelis) is a medium-sized arboreal anuran with adults typically measuring 32–60 mm in snout-vent length (SVL), though most individuals fall within 32–51 mm. The overall build is sturdy and robust, adapted for life in trees and shrubs, distinguishing it from more slender congeners like the squirrel treefrog.^[21]^[3] The skin exhibits a granular, warty texture dorsally, providing a rough surface that aids in camouflage and moisture retention, while the ventral surface is smoother.^[21]^[3] Prominent adhesive toe pads, expanded and equipped with mucous secretions, cover the tips of the digits on both fore- and hind limbs, enabling strong adhesion to vertical surfaces such as bark and leaves.^[21] The hind limbs are long and powerful, facilitating jumps of several body lengths, a key adaptation for escaping predators and navigating arboreal environments; concealed within the inner thighs are bright yellow-orange flash colors that become visible during leaps.^[3] Forelimbs are shorter but similarly equipped with adhesive pads for climbing. The head is broad with a rounded snout, featuring large eyes positioned dorsolaterally and horizontal pupils typical of anurans, enhancing nocturnal vision, and a pale spot beneath each eye.^[21]^[3] A distinct round tympanum lies posterior to each eye, but lacks unique patterning that differentiates it from the morphologically similar gray treefrog (D. versicolor).^[3]

Coloration and camouflage

Cope's gray treefrog displays a variable dorsal coloration ranging from mottled gray to gray-green, typically accented by irregular dark blotches that enhance its cryptic appearance against tree bark. This base hue can shift to include shades of brown or pearl-gray, with greener tones more common in juveniles and during the breeding season.^[21] These variations are influenced by environmental conditions, including substrate color, temperature, and humidity, allowing the frog to better match its surroundings.^[21] The ability to alter coloration is facilitated by dermal chromatophores, specialized pigment cells that redistribute granules in response to physiological cues, enabling physiological color change over periods of hours.^[22] This process supports camouflage by mimicking the mottled patterns of bark on trees and shrubs, thereby reducing predation risk through crypsis. Unlike some other hylid frogs that change color more rapidly, Cope's gray treefrog exhibits a relatively slower adjustment, often taking several hours to fully adapt to new backgrounds.^[23] Sexual dimorphism in coloration is evident during the breeding season, when males develop a distinctive black or dark gray throat, serving as a visual signal to females and conspecifics, while female throats remain pale or whitish.^[24] Additionally, both sexes possess bright yellow to orange patches with black speckling on the inner thighs and groin, which are hidden when at rest but abruptly exposed during leaps.^[21] This flash pattern functions as a deimatic display, potentially startling predators and providing an escape opportunity.^[24]

Distribution and habitat

Geographic range

Cope's gray treefrog (Dryophytes chrysoscelis) is native to the southeastern quadrant of North America, with its range extending from central Texas eastward across Louisiana, Mississippi, Alabama, Georgia, South Carolina, North Carolina, and Virginia, and northward through the Midwest to southern Ontario and Manitoba in Canada. The species reaches its eastern limits along the Atlantic coast, including the Florida panhandle but excluding peninsular Florida. This distribution spans a variety of states including Arkansas, Kentucky, Tennessee, Illinois, Indiana, Ohio, Pennsylvania, and others, reflecting a broad occupancy in lowland and midland regions.^[10]^[25]^[3] In the northern parts of its range, particularly in the Great Lakes region and surrounding areas such as southern Quebec and New England, Cope's gray treefrog occurs sympatrically with the closely related northern gray treefrog (Dryophytes versicolor), where the two species can hybridize but maintain distinction through differences in call and chromosome number.^[10]^[21] The species was originally described in 1880 by Edward Drinker Cope based on specimens collected near Dallas, Texas, establishing its type locality in the southwestern extent of the range. Subsequent 20th-century surveys, including comprehensive herpetological atlases and field guides, have refined the understanding of its range limits, confirming its absence in certain peripheral areas like the Rocky Mountains and peninsular Florida. Currently, the distribution remains stable, with no recorded introduced populations, though anthropogenic factors and climate change may facilitate potential northward expansions, as hypothesized in studies of recent range dynamics in the Midwest.^[2]^[10]^[26]

Habitat preferences

Cope's gray treefrog (Dryophytes chrysoscelis) primarily inhabits wooded areas adjacent to temporary wetlands, favoring deciduous hardwood forests, swamps, bottomland forests, and suburban woodlots that provide proximity to breeding sites such as vernal ponds, marshes, and roadside ditches.^[27] These environments offer a mix of moist, vegetated uplands and seasonal water bodies essential for survival and reproduction.^[28] In terms of microhabitat use, adults are highly arboreal, perching on tree trunks, branches, or bark crevices during the non-breeding season, and occasionally on man-made structures like rain gutters or fences in disturbed areas.^[10] During breeding, individuals shift to ground-level positions near water edges for chorusing, though they remain closely associated with nearby vegetation for refuge.^[29] Studies indicate a strong preference for terrestrial microhabitats within 2 meters of trees, with most individuals captured 1.6–2.0 m from tree bases, highlighting their reliance on arboreal cover adjacent to aquatic zones. Seasonally, non-breeding adults occupy upland forests, often retreating 12–21 m into terrestrial habitats for foraging and shelter, while during the breeding season (typically spring to summer), they migrate to floodplains, ponds, or other low-lying areas for mating aggregations.^[29] This shift underscores their dependence on connected landscapes that link forested uplands with ephemeral wetlands.^[2] The species demonstrates tolerance for disturbed habitats, including urban edges, farmlands, and fragmented woodlands, where it utilizes artificial water sources and suburban greenery.^[28] However, it exhibits a clear preference for mature woodlands with greater than 50% canopy cover, as evidenced by higher oviposition rates in large, closed-canopy patches that reduce desiccation risk and provide structural complexity.^[30] Such preferences suggest that while adaptable, optimal conditions involve intact forest canopies supporting arboreal lifestyles and site fidelity, with individuals showing high return rates to specific perches over multiple seasons.

Reproduction and life cycle

Breeding behavior

Cope's gray treefrogs breed during late spring and summer, typically from late April to August, with activity triggered by warm rains and air temperatures exceeding 15°C. This prolonged breeding period allows multiple reproductive opportunities, as males may call on several nights within a season.^[31]^[6] Males aggregate in choruses at fishless ponds, ditches, or temporary wetlands, perching on vegetation near or above the water to produce advertisement calls that attract females.^[21] These choruses form ensembles where males defend small territories through aggressive calls, often resembling a hen turkey's alarm, to deter rivals and maintain spacing.^[27] The lek-like system emphasizes vocal competition over physical confrontations. During courtship, females approach chorusing males and select mates primarily based on call quality, such as duration and rate, before initiating amplexus.^[32] In axillary amplexus, the pair moves to vegetation over the water surface, where the female deposits eggs in small gelatinous packets while the male fertilizes them externally. Each female produces a single clutch of 1,000–2,000 eggs, divided into 10–40 egg packets attached to submerged or floating vegetation.

Development stages

The development of Cope's gray treefrog (Dryophytes chrysoscelis) begins with the egg stage, where females deposit eggs in small surface films or clusters of 20–40 translucent ova, loosely attached to vegetation in shallow water. These eggs typically hatch in 3–7 days, with the duration influenced by water temperature (e.g., 3–5 days at 20–25°C), rendering them highly vulnerable to predation by insects, fish, and other amphibians during this brief embryonic phase.^[6]^[21] Upon hatching, tadpoles enter the larval stage as primarily herbivorous filter-feeders, consuming algae, organic detritus, and periphyton scraped from substrates, though they can opportunistically ingest higher-protein items for accelerated growth. Over 4–6 weeks, they grow to 20–30 mm in total length, developing in temporary ponds where water quality and food availability shape their survival and size at this stage.^[33]^[6] Metamorphosis follows, typically 45–65 days after egg deposition, as tadpoles undergo rapid physiological changes including tail resorption and lung development, emerging as froglets around 16–25 mm in snout-vent length. These juveniles closely resemble miniature adults in form but initially exhibit subdued coloration and patterns, gradually acquiring full camouflage abilities as they transition to terrestrial life.^[15]^[33] Overall growth rates from egg to maturity are modulated by environmental factors such as temperature, which accelerates development in warmer conditions, and food resources, which influence larval size and metamorphic timing; sexual maturity is attained in 1–2 years, often after the first breeding season.^[6]^[34]

Behavior and ecology

Vocalizations

Cope's gray treefrog (Dryophytes chrysoscelis) produces an advertisement call characterized as a rapid, harsh trill composed of a series of short pulses. The call typically lasts 0.5–1 second, with durations averaging 0.68–0.84 seconds across populations. It features a pulse rate of 34–60 pulses per second, often around 45–50 pulses per second at 20°C, which is notably faster than that of the closely related eastern gray treefrog (D. versicolor). The call exhibits a bimodal frequency spectrum with dominant frequencies around 1,250 Hz and 2,500 Hz, and sound pressure levels averaging 92–93 dB SPL at 1 m in natural conditions.^[35]^[36]^[37] This vocalization primarily functions to attract females during breeding choruses and to repel rival males through species recognition. Female D. chrysoscelis exhibit a strong preference for advertisement calls with higher pulse rates and longer durations, which signal male quality and correlate with increased mating success. The pulse rate is temperature-dependent, increasing with warmer conditions (e.g., from approximately 35 pulses per second at lower temperatures to over 50 at higher ones), allowing females to adjust their preferences accordingly to account for environmental variation in male signaling.^[35]^[36]^[36] Acoustic properties show geographic variation across the species' range, with dialects evident in differences such as call duration and pulse rate between eastern and southwestern Virginia populations, where southwestern calls are shorter and faster on average. These variations aid in local adaptation but maintain sufficient consistency for species-level identification. In field studies, recordings of advertisement calls are essential for distinguishing D. chrysoscelis from morphologically similar species like D. versicolor without relying on genetic testing, as the higher pulse rate provides a reliable acoustic marker even when adjusted for temperature.^[36]^[35]^[36]

Diet and foraging

Cope's gray treefrogs (Dryophytes chrysoscelis) are primarily nocturnal insectivores as adults, feeding on a variety of arthropods including moths, beetles, flies, spiders, plant lice, harvestmen, and mites, as well as occasional non-arthropod prey such as snails and smaller frogs.^[21] They opportunistically consume terrestrial invertebrates that fit within their mouth, swallowing prey whole.^[38] This diet supports their energetic needs during the active season, with feeding often occurring near artificial lights where insects congregate.^[2] Adults employ a sit-and-wait foraging strategy, perching on vegetation or structures in the wooded understory and ambushing passing prey with rapid tongue projection, which can extend up to approximately 1.5 times their body length.^[38] This ambush tactic minimizes energy expenditure while relying on keen vision and camouflage for prey detection and predator avoidance.^[21] Foraging is most active at dusk and night, aligning with peak insect availability. Juveniles, shortly after metamorphosis, consume smaller insects similar to adults but in reduced sizes, supplemented initially by remnants of algae from their tadpole stage.^[21] Feeding intensity varies seasonally, with higher intake during summer months when individuals emerge from daytime refuges to forage, and complete fasting during winter hibernation on land.^[21]

Physiology and adaptations

Freeze tolerance

Cope's gray treefrog (Dryophytes chrysoscelis, formerly Hyla chrysoscelis) exhibits remarkable freeze tolerance, enabling it to survive subzero temperatures during winter hibernation by allowing up to 65% of its body water to freeze extracellularly at temperatures down to -4°C.^[9]^[15] This adaptation is crucial for its survival in temperate regions where it hibernates under leaf litter or bark. During freezing, the frog's heart rate slows dramatically and eventually stops as ice formation halts circulation and respiration; however, these functions spontaneously revive upon thawing without permanent damage.^[9] To mitigate cellular damage from ice crystals, the frog mobilizes cryoprotectants such as glycerol (accumulating up to 200 mM in muscle tissue), glucose (reaching approximately 59 mM in plasma), and urea (around 100 mM in tissues).^[9] These compounds are synthesized in response to cooling and freezing, primarily in the liver, and distributed throughout the body to lower the freezing point of intracellular fluids, prevent excessive dehydration, and stabilize proteins and membranes.^[9] Unlike freeze-avoiding species, Cope's gray treefrog limits supercooling to a moderate range, avoiding the risks of deep supercooling that could lead to rapid, injurious ice formation internally.^[9] Freezing is instead initiated externally through skin contact with ice nuclei, such as frost on surrounding surfaces, promoting controlled extracellular ice growth.^[9] Recovery from freezing occurs over approximately 24 hours at warmer temperatures around 5°C, during which cryoprotectant levels gradually decline as the frog metabolizes them.^[9] Individuals can endure multiple freeze-thaw cycles—up to at least three—without significant harm, though repeated episodes may delay locomotor recovery and deplete hepatic glycogen stores by up to 84%.^[39] This resilience underscores the frog's physiological preparedness for fluctuating winter conditions.

Defensive mechanisms

Cope's gray treefrog employs a combination of chemical and behavioral defenses to deter predators. Its skin produces noxious secretions that render the frog unpalatable, particularly to mammalian predators such as shrews (Blarina brevicauda), causing a burning sensation and inflammation in the mouth upon attack.^[40] These secretions consist of bioactive compounds with antimicrobial properties that provide antipredator protection. Tadpoles lack significant chemical defenses and are considered palatable to many aquatic predators.^[40] Behavioral strategies further enhance survival. During escape jumps, the frog flashes bright yellow or orange coloration on the inner thighs and groin, an aposematic signal that startles or confuses predators, allowing time for evasion; this hidden pattern is typically concealed at rest to maintain crypsis.^[3] Nocturnal activity patterns reduce encounters with diurnal predators like birds, with adults becoming active primarily at dusk or night.^[21] Death feigning, or thanatosis, occurs rarely, particularly in response to handling or capture, where the frog remains motionless to feign death.^[40] Primary predators of adults include snakes, birds such as herons (Ardeidae), and mammals like raccoons (Procyon lotor) and skunks (Mephitis mephitis), which target calling males at breeding sites.^[40] Tadpoles face threats from aquatic insects like diving beetles and odonate naiads, fish such as bluegill sunfish (Lepomis macrochirus), and larger amphibian larvae including tiger salamanders (Ambystoma tigrinum).^[21] These defenses collectively minimize predation risk, though calling males remain vulnerable due to acoustic attraction.^[40]

Conservation

Status

Cope's gray treefrog (Dryophytes chrysoscelis) is classified as Least Concern on the IUCN Red List, with the assessment conducted in 2017.^[41] This status reflects its extensive distribution across the eastern United States and parts of south-central Canada, where it occupies a wide range of habitats without evidence of severe fragmentation or rapid decline.^[41] The species' tolerance to moderate habitat alterations, such as those in forested and suburban woodlands, further supports this classification, as it does not meet the criteria for higher threat categories under IUCN guidelines.^[41] Global population estimates indicate between 100,000 and 1,000,000 individuals, predominantly adults, across its range.^[25] Overall trends are relatively stable, with short-term changes at or below 10% and long-term declines not exceeding 50%, though no significant population crashes have been documented.^[25] Monitoring is particularly recommended at northern range edges, where localized vulnerabilities may occur due to climatic sensitivities.^[25] Regionally, the species holds a global conservation rank of G5 (secure) from NatureServe, indicating it is demonstrably secure across much of its range, including most southern states where it is ranked S5 (secure) in areas like Alabama, Georgia, and Louisiana.^[25] In contrast, it is state-threatened in New Jersey, a status established in 1979 as endangered due to limited distribution and habitat constraints and reclassified to threatened effective January 6, 2025, following a recommendation by the New Jersey Endangered and Nongame Advisory Committee in 2016.^[25]^[42] Similar peripheral concerns exist in other northern states, such as Pennsylvania (S1, critically imperiled), underscoring the need for targeted regional assessments.^[25]

Threats and protection

Cope's gray treefrog (Dryophytes chrysoscelis) faces several primary threats across its range, primarily driven by human activities. Habitat loss and fragmentation due to urbanization, agricultural expansion, and development pose significant risks, particularly the destruction of forested areas and ephemeral woodland ponds essential for breeding.^[43] Road mortality is another key concern during seasonal migrations to breeding sites, where adults and juveniles crossing roadways experience high vehicular collision rates, exacerbating population declines in fragmented landscapes.^[44] Pollutants in breeding ponds, such as pesticides like malathion, adversely affect tadpole survival and development, with sublethal exposures reducing growth and increasing vulnerability to predators.^[45] Climate change further compounds these pressures by potentially shifting the species' range northward and altering breeding phenology through warmer temperatures and changing precipitation patterns. Earlier onset of spring conditions may disrupt synchronized reproduction, affecting larval development timing relative to food availability and predator cycles.^[46] Conservation efforts for Cope's gray treefrog include habitat protections within national forests and wetlands, where federal lands safeguard key breeding sites from development. In sensitive regions like New Jersey, the species is state-listed as threatened, with regulations prohibiting take and mandating habitat preservation.^[44]^[42] Ongoing monitoring by the U.S. Geological Survey's Amphibian Research and Monitoring Initiative (ARMI) tracks population trends and threats, while the IUCN assesses it as Least Concern globally, emphasizing regional vulnerabilities.^[10] Mitigation strategies focus on wetland restoration through programs like the USDA's Wetland Reserve Program, which recreates ephemeral ponds to support breeding. Additionally, avoiding fish stocking in potential breeding sites prevents predation on tadpoles, as the species preferentially oviposits in fish-free waters to enhance offspring survival.^[47]^[48]

References

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Hyla femoralis chrysoscelis Cope, 1880 ; Hyla versicolor sandersi Smith and Brown, 1947 ; Common Name(s):, Cope's Gray Treefrog [English] ; Taxonomic Status:.
[2]
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Cope's Gray Treefrog (Hyla chrysoscelis)
Family: Hylidae. Adult Description: The Cope's Gray Treefrog medium-sized frog with adults usually ranging from 1–2 inches (2.5–5 cm) in length.
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Also known as Cope's gray treefrog, this species has a robust body, stubby limbs, and a short rounded head with large eyes.
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Species: chrysoscelis is derived from the Greek words chryso which means 'gold' and kelis which means "a spot".
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[40]
Hidden black and yellow thigh color acts as an aposematic signal in ...
Sep 5, 2023 · We investigated whether the conspicuous black and yellow spotted pattern on the thighs of Eastern Gray Treefrogs (Hyla versicolor) serve as an aposematic ...Missing: inflation | Show results with:inflation
[41]
[PDF] Antipredator Mechanisms of Post-Metamorphic Anurans
May 1, 2019 · ... (Brodie. 702 and Formanowicz 1981; Toledo et al. 2015). 703. Distress calls may be emitted during expiration, when disinflation of the lungs ...
[42]
The IUCN Red List of Threatened Species
Insufficient relevant content. The provided URL (https://www.iucnredlist.org/species/55448/196334128) does not contain the requested information (IUCN status, assessment year, population estimate, trends, reasons for classification). The page content is limited to a feedback form for Google Translate and does not provide species-specific data.
[43]
Cope's Gray Treefrog | Nebraskaland Magazine
Apr 3, 2024 · Cope's gray treefrog is a small, gray/green amphibian with markings, a dark mask, and adhesive toe pads for climbing. It is nocturnal and has a ...Missing: facts | Show results with:facts
[44]
Cope's gray treefrog - Upper Midwest Environmental Sciences Center
Amphibian Research and Monitoring Initiative, Midwest Region. Cope's gray treefrog (Hyla chrysoscelis). Species per monitoring area. Cope's gray treefrog ...
[45]
Single and interactive effects of malathion, overwintered green frog ...
We examined the effects of the insecticide malathion, larger tadpole ... on tadpoles of Cope's gray treefrog (Hyla chrysoscelis) reared from hatching through ...Missing: pollutants | Show results with:pollutants
[46]
[PDF] Community-Level Response to Climate Change: Shifts in Anuran ...
Sep 10, 2012 · We sought to explore how climate change affects reproductive phenology within a community of spring and summer breeding amphibians. In ...
[47]
[PDF] WRP Contributes to Amphibian Conservation in Missouri
Hyla chrysoscelis- Hyla versicolor complex. Grey treefrogs, Eastern and ... Wetland restoration efforts on. WRP sites in the Lower Grand River. Basin.
[48]
Mosquitofish dominate amphibian and invertebrate community ...
Jul 25, 2013 · Implementing these recommendations will improve the conservation potential of restored wetlands. ... Grey treefrogs Hyla versicolor/chrysoscelis ...