Smooth softshell turtles are native to temperate areas of North America, ranging throughout the central and south-central United States. Their range extends from Pennsylvania to New Mexico and south to the Florida panhandle. This species is thought to have been extirpated from Pennsylvania. Smooth softshell turtles are believed to have occurred in North America since the Cretaceous Period, although this is not yet supported by fossil evidence. Smooth softshell turtles have also been introduced to France. (Ernst and Lovich, 2009; Hulse, et al., 2001; Oldfield and Moriarty, 1994; Quammen, 1992)
Two subspecies of smooth softshell turtles have been identified. Midland smooth softshells, Apalone mutica mutica, are found throughout the central United States, while Gulf coast smooth softshells, Apalone mutica calvata, range from Louisiana to the panhandle of Florida. (Ernst, et al., 1994)
Smooth softshell turtles are typically found along major riverine systems such as the Ohio, Missouri, and Mississippi rivers. They prefer large rivers and streams with medium to fast currents . Within river systems, smooth softshell turtles had highest populations in the open side channels and main channels of the Mississippi and Ohio Rivers in southern Illinois. Despite their preference for riverine systems, smooth softshell turtles have also been found in lakes, bogs, ponds, and drainage ditches. They generally prefer areas of sandy or mucky bottoms with little aquatic vegetation, and they avoid aquatic systems with a rocky substrate. (Barko and Briggler, 2006; Bodie, et al., 2000; Ernst and Barbour, 1989; Ernst and Lovich, 2009; Oldfield and Moriarty, 1994)
Smooth softshell turtles have microhabitat preferences within the Kansas River in Kansas. Males were observed more frequently than subadult and adult females in shallow depths along the river. Hatchlings also preferred shallow areas along the river, most likely to avoid larger aquatic predators. (Plummer, 1977)
Of the subspecies of smooth softshell turtles, Gulf coast smooth softshells (Apalone mutica calvata), have been found only in riverine and stream systems, while midland smooth softshells, (Apalone mutica mutica), have also been observed inhabiting lakes, bogs, drainage ditches, and ponds. (Ernst and Lovich, 2009; Oldfield and Moriarty, 1994)
Smooth softshell turtles are medium to large freshwater turtles. Females have a back shell that is 16.5 to 35.6 cm long. Females are larger than males, who have a shell that is 11.5 to 26.6 cm long. Like other softshell turtles, smooth softshell turtles have a carapace that is covered by skin instead of the hard scutes commonly observed in other turtle species. The carapace is ovoid and lacks spines on the front edge. The coloring of the carapace ranges from olive to orange. Females typically have a tan or brown carapace, while males have a brown or gray carapace. Both sexes have dark markings (spots, streaks, or blotches) on their carapace, although females typically have a blotchier pattern. The plastron is light (white or gray) with no markings, and the underlying bones are visible. Dorsal coloration of an individual's head, limbs, and tail are similar to that of its carapace. A cream or orange line bordered in black extends from the back of each eye to the neck. Juvenile smooth softshell turtles do not differ in coloration from adults, but juveniles of subspecies are used to tell them apart in the field. Hatchlings have a brown or olive carapace with many markings on the carapace. (Ernst and Lovich, 2009; Minnesota Department of Natural Resources, 2011; Oldfield and Moriarty, 1994)
Smooth softshell turtles have a tubular snout with round nostrils that are usually positioned inferior, and they lack a septal ridge. Male smooth softshell turtles have thicker tails than females, a trait commonly observed in turtle species. In males, the anal vent is located near the tip of the tail, while in females, the anal vent is usually located near the edge of or under the carapace. As with other species of turtles, female smooth softshells have longer hind claws than males, which have longer foreclaws than females. (Ernst and Lovich, 2009)
Smooth softshell turtles are the most aquatic of all North American softshells. Their aquatic nature is made possible by a variety of behavioral and morphological adaptations. The skin covering the shell causes a high rate of water exchange. Water exchange in freshwater is typically 6.3 mL/100g wet BM/hour. The lining of the cloaca and pharynx enables uptake of oxygen from the water. Furthermore, the surface of their shell and skin is cutaneous, increasing the permeability of gases and water. For instance, smooth softshell turtles lose about 64% of respiration-produced carbon dioxide through their skin. Their long neck and snout contribute to the ability to remain submerged for extensive periods of time. (Ernst and Lovich, 2009; Jackson, et al., 1976; Oldfield and Moriarty, 1994; Stone and Iverson, 1999)
Smooth softshell turtles are mostly easily confused with spiny softshell turtles (Apalone spinifera). The two species, however, can be distinguished by examining the carapace. Spiny softshells have spines along the front edge of their carapace, and the carapace usually has a sandpaper texture. Smooth softshells lack these characteristics. Spiny softshells, as with most softshell turtles, also have a septal ridge in the nose. However, smooth softshells lack a septal ridge. Distinguishing features of other softshell species include heavily marked limbs and spines on the carapace. (Ernst and Lovich, 2009; Oldfield and Moriarty, 1994)
Embyonic development of smooth softshell turtles is categorized into three stages: division of cells and tissue development, organogenesis, and the growth of the embryo before the hatching stage. The timing of these three stages is related to three equal corresponding periods during incubation. Sex determination is not temperature dependent, and relatively equal proportions of hatchlings are male and female. (Ernst and Lovich, 2009; Ewert, 1985; Nagle, et al., 2003)
With time, the round shape of a hatchling smooth softshell turtle's carapace changes to an oval shape through allometric growth. There is no change, however, in plastron shape as the hatchling grows, making for little change in the straight carapace length/plastron length (SCL/PL) ratio. Once the plastron has reached a minimum length of 60 mm, individuals can be sexed using physical characteristics described above. Unlike many other species of turtles, smooth softshell turtles do not form growth annuli on their shells, making them difficult to age in the field. (Ernst and Lovich, 2009)
Growth of smooth softsell turtles typically occurs from May to September, and growth rates are usually highest from June to August. Males grow on average 1.95 mm/month when between lengths of 61 and 65 mm. At a plastron length (PL) of 66 to 75 mm, males grow at a rate of 2.1 to 2.5 mm/month. This rate decreases to 0.09 mm/month when males reach a PL of 111 to 115 mm. Females exhibit a faster growth rate than males. In females with a PL of 61 to 70 mm, growth rate is 2.8 mm/month. This decreases to 0.7 mm/month at a PL of 151 to 160 mm. Most species of turtles experience indeterminate growth, although this has not verified for this species. (Browne and Hecnar, 2007; Ernst and Lovich, 2009; Plummer, 1977)
Breeding activity of smooth softshell turtles occurs from April to June and possibly into September. Males seek out females by approaching other adults. If the approached individual is male, the response to the investigation is usually passive but can be aggressive on occasion. Non-receptive females are often aggressive; during the breeding season many males are observed with wounds inflicted by females. Receptive females, on the other hand, are passive to the advances of a male. Many males may be present near a receptive female, and all may attempt to mate with her. When there is only one male present, the female may chase the male. (Ernst and Lovich, 2009; Oldfield and Moriarty, 1994)
Copulation almost always occurs in the water, and a sexually receptive female is mounted from behind. Deep water is usually needed to successfully mount a female and a male must swim in place for upwards of 20 min to keep his position. During this time, the male needs to keep its vents aligned. (Ernst and Barbour, 1972; Ernst and Lovich, 2009)
Smooth softshell turtles nest between late May and July. In more northern locations such as Minnesota and Wisconsin, nesting typically takes place from June to early July. Any disturbance can cause early abandonment of the nest by wary females. Females dig a nest cavity 15 to 30 cm deep with their hind feet. Nests are typically located on a sand bar with little vegetation, although some nests have been found in dense vegetation. Nests are generally located within 18 m of the water and only rarely are more than 30 m away from water. Nests are usually 0.5 to 6.1 m above the water. Nest density can be quite high, and in some cases there are connecting chambers between nests. Oviposition usually occurs in the early morning. Eggs are laid in two layers in the nesting chamber. Females cover their eggs with sand using their hind feet. A female then usually burrows a tunnel and places herself on the opposite end of the nest. This tunnel can be up to 4 m in length. (Ernst and Lovich, 2009; Oldfield and Moriarty, 1994; Plummer, 1976; Vogt, 1981)
Female smooth softshell turtles lay only one clutch per year. Average clutch size is 15 to 25 eggs. The minimum observed clutch size is 1 egg while the maximum clutch size observed is 33 eggs. Clutches laid later in the season are usually smaller in size than early season clutches. The size of a clutch is proportional to the straight carapace length (SCL) of the female. Eggs are a spheroidal shape and resemble ping-pong balls. In a typical clutch, 75% of eggs are likely to survive. Predation and flooding can have large effects on egg survival. ("Smooth softshell (Apalone mutica)", 2009; Doody, 1996; Ernst and Barbour, 1972; Ernst and Lovich, 2009; Oldfield and Moriarty, 1994; Plummer, 1976)
Eggs generally hatch in 8 to 12 weeks. Hatching frequency is highest in August to September. Hatchlings use their front claws to break through the egg, relying on their claws more than their caruncle (egg tooth), which is less used in comparison to other species. Hatchlings generally emerge from the nest around sunset. At the moment of hatching, hatchlings are completely independent. Recently hatched smooth softshell turtles average 4 cm in straight carapace length and have a body mass of 3.0 to 7.5 g (mean 5.4 g). Caruncles drop off in a week, and the umbilical scar is usually 2 mm in diameter. (Ernst and Lovich, 2009; Oldfield and Moriarty, 1994)
Male smooth softshell turtles become sexually mature during their fourth year with mean plastron length (PL) ranging from 80 to 85 mm. Females become sexually mature during their ninth year with mean PL ranging from 140 to 150 mm. Mature individuals attempt to mate immediately upon emergence from hibernation. The volume of mature male testes varies with season, with testes reaching a maximum diameter immediately before hibernation. In April and May, the vas deferens of males become swollen, 2 mm in diameter. The vas deferens is no longer swollen by June but become swollen with sperm once more by October. Vitellogenesis in females begins in July in Kansas. ("Smooth softshell (Apalone mutica)", 2009; Doody, 1996; Ernst and Barbour, 1972; Ernst and Lovich, 2009; Oldfield and Moriarty, 1994; Plummer and Shirer, 1975; Plummer, 1977)
Smooth softshell turtles provide prenatal care for their offspring. Females produce high levels of non-polar lipids that provide energy for their growing embryos. They produce energy at a level much higher than what is necessary to keep the embryos alive, which is known as parental investment in embryogenesis. At birth, hatchlings have high concentrations of lipids. These act as a food source until they are mature enough to begin feeding. This allocation of energy into high storage reserves for hatchlings represents parental investment in care. This provisioning of lipids enables hatchlings to survive in areas that have low resource availability. (Ernst and Lovich, 2009; Nagle, et al., 2003)
Unlike many other species of turtles, smooth softshell turtles do not form growth annuli on their shells, which makes them very difficult to age in the field. The lifespan of this species is unrecorded. Individuals in captivity have lived over 11 years, and they are believed to be capable of living 20 years. Florida softshell turtles (Apalone ferox) and spiny softshell turtles (Apalone spinifera) can live up to 25 years in captivity. (Ernst and Lovich, 2009; Snider and Bowler, 1992)
Smooth softshell turtles are the most aquatic of all North American softshells. Behavioral and morphological adaptations permit their aquatic nature. Smooth softshell turtles are able to remain submerged for extensive periods of time, which is made possible in part by their long neck and snout. They often bury themselves in the substrate of a body of water deep enough so their snout just barely reaches the surface. To achieve this position, a smooth softshell turtle pushes itself head-first into the sediment; it pulls itself with its frontlimbs while pushing with its hindlimbs. When its body is positioned tilting downward toward the front, it stirs up the sediment. The falling material covers the turtle so only its head is visible. (Ernst and Lovich, 2009; Jackson, et al., 1976; Oldfield and Moriarty, 1994)
Smooth solfshell turtles hibernate by burying themselves in substrate underwater. They emerge from winter hibernation in March or early April in Kansas and in May in northern areas such as Minnesota and Wisconsin. Activity of smooth softshell turtles is typically observed from May through September. In more southern regions such as New Mexico, members of this species are usually active from April to October. After emerging from hibernation, smooth softshell turtles are often observed basking on sand bars or in shallow water between 0700 and 1700 hours. Sandy and muddy bars within a few meters of the water's edge are preferred basking sites, although logs and rocks near the water may also be used. When basking, smooth softshell turtles extend their neck and tuck their limbs into their shell. (Degenhardt, et al., 1996; Ernst and Lovich, 2009; Lindeman, 2000; Plummer, 1977; Vogt, 1981)
Smooth softshell turtles are wary and abandon their basking place if danger is perceived. They are highly agile, both in water and on land, which permits quick escape from predators as well as feeding on fast-moving prey. Members of this species are generally solitary. (Ernst and Lovich, 2009; Oldfield and Moriarty, 1994)
Smooth softshell turtles primarily interact through visual and tactile cues. When seeking out mates, males physically investigate females. Although little information was found regarding perception and communication by this species, a close relative, spiny softshell turtles (Apalone spinifera), perceives its environment using chemical, visual, and tactile cues, vibrations and communicates using tactile cues. (Bartholomew, 2002; Ernst and Lovich, 2009)
Smooth softshell turtles are carnivorous, eating a variety of organisms including fish, amphibians (adults and larvae), arthropods, spiders (Araneae), snails (Campeloma), mollusks, isopods (Isopoda), millipedes (Diplopoda), and worms (Annelida). Although A. mutica is a dietary generalist, it can be classified as an insectivore. Arthropods typically consumed by smooth softshell turtles are aquatic and larval forms of Coleoptera, Diptera, Calliphoridae, Chironomidae, Cyclorrhapha, Empidae, Muscidae, Ephemeroptera, Tipulidae (Tipulo bicornis), Hemiptera, Hymenoptera, Homoptera, Isoptera, Lepidoptera, Ichneumonidae, Odonata, Neuroptera, Orthoptera, Plecoptera, and Trichoptera. Fish species consumed by smooth softshell turtles include Castostomus commersoni, Cyprinella whipplei, Cyprinella spiloptera, Lepomis macrochirus, Morone chrysops, Hypentilium nigricans, Perca flavescens, and Salvelinus fontinalis. Although primarily carnivorous, smooth softshell turtles occasionally eat vegetation such as algae, potatoes, seeds, stems, mulberry (Morus), fruits, and hard nuts. (Ernst and Lovich, 2009; Oldfield and Moriarty, 1994)
Smooth softshell turtles hunt on both land and in water. They are ambush predators; while concealed in substrate, they use their long neck to grab passing prey. They have also been observed pharyngeal gulping, in which they suck in nearby small prey organisms. They also use their nose to seek food in sediment and vegetation. Females generally utilize deeper water to obtain food, while males tend to forage in shallow water near the shore. Although foraging area differs between sexes, food size does not vary with size or sex. (Ernst and Lovich, 2009; Oldfield and Moriarty, 1994; Plummer and Farrar, 1981)
Due to their high agility on land and water and these avoidance strategies, adults have few natural predators. Humans and alligators are the main predator of adults. Predators of hatchlings include fish, other turtles (common snapping turtles, alligator snapping turtles, possibly adult Apalone), water snakes, shoreline birds, bald eagles, and other mammals. Nest predation is usually from raccoons, skunks (Memphitis and Spilogale), crows, fire ants (Solenopsis invicta), fly larvae (Sarcophagidae), dogs, red foxes, moles (eastern moles, and other small mammals. (Doody, 1996; Ernst and Lovich, 2009; Fitch and Plummer, 1975; Oldfield and Moriarty, 1994; Watermolen, 2004)
Smooth softshell turtles are wary and abandon their basking place if danger is perceived. They are highly agile, both in water and on land, which permits quick escape from predators. They also use their strong diving ability to flee predators and conceal themselves in mud. When caught by predators, a smooth softshell turtle pulls itself into its shell. (Ernst and Lovich, 2009; Oldfield and Moriarty, 1994)
In some regions, adults and eggs are gathered for food. Additionally, this species is occasionally a part of the pet trade. (Ernst and Lovich, 2009)
Although smooth softshell turtles may prey upon game fish, their impact on fish populations is believed to be insignificant. There are no known adverse effects of smooth softshell turtles on humans, although they may bite when handled. (Ernst and Barbour, 1972)
Although smooth softshell turtles are listed as a speices of least concern by the IUCN, little data is available to make a confident assessment. Currently, this species is widespread and locally common, suitable habitat is present, and harvest rates do not contribute to decline. Smooth softshell turtles are listed as a species of special concern in the state of Minnesota. Their slow maturation rate increases time necessary to restore populations. (Ernst and Lovich, 2009; Minnesota Department of Natural Resources, 2011; Moll and Moll, 2000; Pappas, et al., 2001; van Dijk, 2010)
Their ability to absorb oxygen from the water has made smooth softshell turtles susceptible to water pollution. Other negative impacts include habitat degradation, harvesting for food, changes in hydrological regimes (construction of dams and locks), and an increase in human disturbances at nesting sites. Human disturbance includes boating near nest sites, with waves resulting from boat use causing erosion and egg exposure. This species is also caught as bycatch (capture of non-target species) in the commercial fishing industry. (Ernst and Lovich, 2009; Ernst, et al., 1994; Minnesota Department of Natural Resources, 2011; Moll and Moll, 2000; Pappas, et al., 2001; Trauth, et al., 2004)
Efforts to conserve smooth softshell turtle should include the protection of waterways and surrounding terrestrial land that are known to support large populations of this species. Upstream sites should also be protected. Protected areas ideally should include basking and nesting habitats with high densities of prey, hibernation areas, and be of ample size to support home ranges. (Ernst, et al., 1994; Minnesota Department of Natural Resources, 2011; Moll and Moll, 2000)
Jeana Albers (author), Minnesota State University, Mankato, Robert Sorensen (editor), Minnesota State University, Mankato, Gail McCormick (editor), Animal Diversity Web Staff, Catherine Kent (editor), Special Projects.
living in the Nearctic biogeographic province, the northern part of the New World. This includes Greenland, the Canadian Arctic islands, and all of the North American as far south as the highlands of central Mexico.
living in the northern part of the Old World. In otherwords, Europe and Asia and northern Africa.
having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.
a wetland area rich in accumulated plant material and with acidic soils surrounding a body of open water. Bogs have a flora dominated by sedges, heaths, and sphagnum.
an animal that mainly eats meat
flesh of dead animals.
uses smells or other chemicals to communicate
animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature
A substance that provides both nutrients and energy to a living thing.
mainly lives in water that is not salty.
the state that some animals enter during winter in which normal physiological processes are significantly reduced, thus lowering the animal's energy requirements. The act or condition of passing winter in a torpid or resting state, typically involving the abandonment of homoiothermy in mammals.
Animals with indeterminate growth continue to grow throughout their lives.
An animal that eats mainly insects or spiders.
referring to animal species that have been transported to and established populations in regions outside of their natural range, usually through human action.
offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).
marshes are wetland areas often dominated by grasses and reeds.
having the capacity to move from one place to another.
specialized for swimming
the area in which the animal is naturally found, the region in which it is endemic.
reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.
the business of buying and selling animals for people to keep in their homes as pets.
having more than one female as a mate at one time
Referring to something living or located adjacent to a waterbody (usually, but not always, a river or stream).
breeding is confined to a particular season
reproduction that includes combining the genetic contribution of two individuals, a male and a female
a wetland area that may be permanently or intermittently covered in water, often dominated by woody vegetation.
uses touch to communicate
that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).
movements of a hard surface that are produced by animals as signals to others
uses sight to communicate
2009. "Smooth softshell (Apalone mutica)" (On-line). Wisconsin Department of Natural Resources. Accessed April 15, 2011 at http://dnr.wi.gov/org/land/er/biodiversity/index.asp?mode=info&Grp=49&SpecCode=ARAAG01020.
Barko, V., J. Briggler. 2006. Midland smooth softshell (Apalone mutica) and spiny softshell (Apalone spinifera) turtles in the middle Mississippi River: Habitat associations, population structure, and implications for conservation. Chelonian Conservation and Biology, 5: 225-231.
Bartholomew, P. 2002. "Spiny softshell turtle" (On-line). Animal Diversity Web. Accessed April 15, 2011 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Apalone_spinifera.html.
Bodie, J., R. Semlitsch, R. Renken. 2000. Diversity and structure of turtle assemblages: Associations with wetland characters across floodplain landscape. Ecography, 23: 444-456.
Browne, C., S. Hecnar. 2007. Species loss and shifting population structure of freshwater turtles despite habitat protection. Biological Conservation, 138: 421-429.
Degenhardt, W., C. Painter, A. Price. 1996. Amphibians and reptiles of New Mexico. Albuquerque, New Mexico: University of New Mexico Press.
Doody, J. 1996. Summers with softshells. Bulletin of Chicago Herpetological Society, 31: 132-133.
Ernst, C., R. Barbour. 1972. Turtles of the United States. Lexington, Kentucky: University Press Kentucky.
Ernst, C., R. Barbour. 1989. Turtles of the World. Washington D.C.: Smithsonian Institution Press.
Ernst, C., R. Barbour, J. Lovich. 1994. Turtles of the United States and Canada. Washington D.C.: Smithsonian Institution Press.
Ernst, C., J. Lovich. 2009. Turtles of the United States and Canada. Baltimore, Maryland: The John Hopkins University Press.
Ewert, M. 1985. Embryology of turtles. Pp. 75-268 in C Gans, F Billett, P Maderson, eds. Biology of the Reptilia, Vol. 14. New York, New York: John Wiley and Sons.
Fitch, H., M. Plummer. 1975. A preliminary ecological study of the soft-shelled turtle Trionyx muticus in the Kansas River. Israel Journal of Zoology, 24: 28-32.
Hulse, A., C. McCoy, E. Censky. 2001. Amphibians and reptiles of Pennsylvania and the Northeast. Ithaca, New York: Cornell University Press.
Jackson, D., J. Allen, P. Strupp. 1976. The contribution of non-pulmonary surfaces to CO2 loss in 6 species of turtles at 20 C. Comparative Biochemistry and Physiology, 55A: 243-246.
Lindeman, P. 2000. Resource use of five sympatric turtle species: Effects of competition, phylogeny, and morphology. Canadian Journal of Zoology, 78: 992-1008.
Minnesota Department of Natural Resources, 2011. "Apalone mutica" (On-line). Minnesota Department of Natural Resources. Accessed April 03, 2011 at http://www.dnr.state.mn.us/rsg/profile.html?action=elementDetail&selectedElement=ARAAG01020.
Moll, E., D. Moll. 2000. Conservation of river turtles. Pp. 126-155 in M Klemens, ed. Turtle Conservation. Washington D.C.: Smithsonian Institution Press.
Nagle, R., M. Plummer, J. Congdon, R. Fischer. 2003. Parental investment, embryo growth, and hatchling lipid reserves in softshell turtles (Apalone mutica) from Arkansas. Herpetologica, 59: 145-154.
Oldfield, B., J. Moriarty. 1994. Amphibians & Reptiles Native to Minnesota. Minneapolis, Minnesota: University of Minnesota Press.
Pappas, M., J. Congdon, A. Pappas. 2001. Weaver Bottoms 2001 turtle survey: management and conservation concerns. Nongame Wildlife Survey, Minnesota Department of Natural Resources and U.S. Fish and Wildlife Service.
Plummer, M. 1977. Activity, habitat, and population structure in the turtle, Trionyx muticus. Copeia, 3: 431-440.
Plummer, M. 1976. Some aspects of nesting success in the turtle, Trionyx muticus. Herpetologica, 32: 353-359.
Plummer, M., D. Farrar. 1981. Sexual dietary differences in a population of Trionyx muticus. Journal of Herpetology, 15: 175-179.
Plummer, M., H. Shirer. 1975. Movement patterns in a river population of the softshell turtle Trionyx muticus. University of Kansas Museum of Natural History Occasional Papers, 43: 1-26.
Quammen, R. 1992. A latest Cretaceous (Maestrictian) lower vertebrate faunule from the Hell Creek Fromation of North Dakota. Proceedings of the North Dakota Academy of Science, 46: 41.
Snider, A., J. Bowler. 1992. Longevity of Reptiles and Amphibians in North American Collections. Pp. 1-44 in J Collins, ed. Herpetological Circular, Vol. 21. Utah: Society for the Study of Amphibians and Reptiles.
Stone, P., J. Iverson. 1999. Cutaneous surface area in freshwater turtles. Chelonian Conservation and Biology, 3: 512-515.
Trauth, S., H. Robison, M. Plummer. 2004. The amphibians and Reptiles of Arkansas. Fayetville: University of Arkansas Press.
Vogt, R. 1981. Natural History of Amphibians and Reptiles of Wisconsin. Wisconsin: Milwaukee Public Museum.
Watermolen, D. 2004. Softshell turtles (g. Apalone) as bald eagle prey. Bulletin of Chicago Herpetological Society, 39: 69-70.
van Dijk, P. 2010. "Apalone mutica" (On-line). In: IUCN 2011. IUCN Red List of Threatened Species. Version 2011.1. Accessed July 05, 2011 at http://www.iucnredlist.org/apps/redlist/details/165596/0.