Geographic Range
Emydura subglobosa
is found on islands and rivers in coastal Australia and New Guinea, such as Fraser
Island, the Jardine River, Daru, Cape York, Stradbroke Islands, and the islands in
Torres Strait (Legler and Georges, 1993). These turtles also occur in lowland swamps,
which cover large areas of the tropical, open plains in western Papua New Guinea (Georges
Guarino and Bito, 2006).
- Biogeographic Regions
- australian
- Other Geographic Terms
- island endemic
Habitat
Preferred habitat of red-bellied short-necked turtles are rivers, swamps, and ponds
of Papua New Guinea and Australia (Georges et al. 2008). In the lower Kikori and Omati
rivers they inhabit slow-moving waters, swamps, and seasonal wetlands (PNG Gas Project,
2005). Like other freshwater turtles, red-bellied short-necked turtles alternate periods
in the water with time basking to raise body temperature (Webb, 1978). Most of their
life is spent in water, where they forage for food. If there is a water scarcity in
hotter months, they move to flooded areas (Georges, Guarino and Bito, 2006).
- Habitat Regions
- temperate
- terrestrial
- freshwater
- Aquatic Biomes
- lakes and ponds
- rivers and streams
- temporary pools
- Other Habitat Features
- riparian
Physical Description
Red-bellied short-necked turtles have olive-colored heads with a yellow-cream stripe
running from the tip of the nose through the eye and into the iris (Georges et al.
2008). A black spot is always present in front of and behind the pupil in
Emydura victoriae
and variable in
Emydura tanybaraga
(Thomson, 2003). They have a prominent upper jaw and two yellow whiskers on the chin;
the same yellow coloration runs along the light-colored jaw line. The upper neck region
is dark gray and the lower, light gray with red streaks running along it. This same
coloration appears on the bottom jaw and belly of the turtle, although the color can
vary among bright orange, yellow, or pink (Legler and Georges, 1993; Ernst and Barbour,
1989). The limbs, tail, plastron, and abdominal regions are all marked with red (Ernst
and Barbour, 1989). Young red-bellied short-necked turtles generally have brighter
markings that fade as they grow, with their red color turning pinkish with time (Ernst
and Barbour, 1989). Females are larger in carapace length, but have shorter tails.
Male carapaces range from 13.3 to 17.3 cm, female carapaces range from 15.2 to 25.5
cm.
Red-bellied short-necked turtles are members of the family of side-necked freshwater
turtles,
Chelidae
. They can be characterized by how they extend and retract their necks. They lay their
neck and head sideways, underneath the upper edge of the shell (Werneburg et al.,
2009).
- Other Physical Features
- ectothermic
- heterothermic
- bilateral symmetry
- Sexual Dimorphism
- female larger
- sexes shaped differently
Development
In many marine, freshwater, and terrestrial turtles, the gender of the embryo is influenced
by incubation temperature. However, this is not the case with Australian
chelids
studied to date, which lack temperature dependent sex determination (Georges and
Legler, 1993).
Following pipping (breaking of the shell), hatchlings remain for a day or so in the
eggshell, where they survive on the remains of the yolk sac (Georges et al., 2007).
Research suggests that these turtles grow at a faster rate prior to maturity, when
growth rates drop abruptly to provide sufficient resources for reproduction (Georges,
1995). The estimated age at sexual maturity is 14 years for males and 9 years for
females
The greatest expected lifespan for
chelid
turtles is estimated at about 100 years for both sexes (Martins and Souza, 2008).
In
Emydura
and
Chelodina
species, females tend to grow faster, reaching larger carapace lengths than males.
The shells of females have a tendency to be deeper and more spacious than the males
to facilitate the storage of eggs (Georges and Legler, 1993).
- Development - Life Cycle
- indeterminate growth
Reproduction
Emydura
species mate year-round, with peaks in the spring and fall. Males of
Emydura
species have sperm all year in the epididymides. Females of
Emydura
species accumulate yolk in the ovaries in late summer through winter.
During the breeding season, males communicate with females with a series of signaling
postures, including a combination of simultaneous stroking, eye blinking, and head
bobbing. The female may be stationary or swimming; when she stops the encounter and
surfaces, the male quickly assumes a nose-to-nose position, performing nose squirts.
Males and females continue bobbing their heads in alternating sequence as they align
their bodies. Once this maneuver is complete the mating begins (Georges & Legler,
1993). During mating, the cloacas touch. They remain together for many hours, although
copulation may only occur for a short time. This mating process may occur more than
once for up to several days, and may involve multiple partners at any given time.
Red-bellied short-necked turtles have scent glands in their carapace that produce
odors used during competition between males during breeding season.
- Mating System
- polygynandrous (promiscuous)
In red-bellied short-necked turtles, females have a large area inside their carapace
to store eggs, whereas males have a larger tail.
Ovulation and nesting begins in early spring. Only female turtles leave the water
during the night or early morning to deposit eggs in hollow cavities constructed in
sand or soil. Females lay eggs within about an hour.
Emydura subglobosa
,
Elseya novaeguineae
, and
Carettochelys insculpta
lay their eggs in the soil of the forest floor, often near the base of trees or in
the sandy soil of freshwater swamps during the late, dry season between August and
October (Georges, 2007; Georges et al., 2006).
Emydura subglobosa
individuals lay white, calcareous, ellipsoid eggs averaging 35.0 ±0.05 mm long and
19.0 ±0.02 mm wide. Estimated mean egg weight of eggs is 7.68 ±0.20 g.
These turtles can produce two to four clutches a year, laying from four to eleven
eggs each time, with an average of 7 eggs in each clutch (Georges et al., 2006).
Eggs incubate and hatch the following dry season in July through August. Many factors
can impact the incubation and hatching period: ambient temperatures, cloud cover,
river levels and flow, tides, and the phase of the moon. High temperatures promote
early hatching and cold temperatures promote later hatching times. Hatchlings make
their journey to freshwater without parental guidance or protection (Georgeset al.,
1993). Red-bellied short-necked turtles typically mature between 7 and 12 years old
with both males and females maturing at carapace lengths of 14 to 15 cm (Georges et
al., 2006).
- Key Reproductive Features
- iteroparous
- seasonal breeding
- gonochoric/gonochoristic/dioecious (sexes separate)
- sexual
- oviparous
After digging a cavity and depositing eggs, female red-bellied short-necked turtles
immediately return to freshwater, leaving the eggs uncovered. In contrast, other turtles
painstakingly cover a cavity after depositing eggs.
Emydura macquarii
drops its shell hard onto the ground to compact the soil in the filled nest. This
tamping of the soil has been observed also in
Chelodina longicollis
,
Chelodina oblonga
,
Chelodina expansa
and
Pseudemydura umbrina
as a way of protection against predators.
Red-bellied short-necked turtles abandon their eggs once they are laid and do not
protect the hatchlings (Georges, Limpus & Parmenter, 1993).
- Parental Investment
- no parental involvement
-
pre-fertilization
- provisioning
Lifespan/Longevity
Red-bellied short-necked turtles have been reported to live 15 to 20 years in captivity.
Behavior
Red-bellied short-necked turtles swim and bask to control internal body temperatures.
During the basking process, tears run down the side of the turtle’s head and into
the mouth while the mouth opens and closes, known as gular movements. Panting and
frothing at the mouth has been observed, although it is more common in
Emydura macquarii
than in the other
Emydura
species. Wetting of the head or limbs, removing the extremities from direst exposure
to heat, and changes to breathing patterns are all mechanisms that prevent over-heating
(Webb, 1978).
Red-bellied short-necked turtles, like other short-neck turtles, snap and bite when
threatened, delivering painful wounds. They tuck in their head while tilting their
shell towards the predators to reduce damage to soft body parts (Legler and Georges,
1993).
- Key Behaviors
- natatorial
- diurnal
- motile
- sedentary
- aestivation
- solitary
Home Range
Red-bellied short-necked turtles do not actively defend a territory.
Communication and Perception
Red-bellied short-necked turtles have highly developed senses necessary for communication
and perception. These senses assist them in locating food, avoiding predators, and
finding mates during the breeding season. Studies have shown that these freshwater
turtles can communicate with each other via a wide range of vocalizations that are
too soft for humans to hear. Evidence also suggests that echolocation may be developed
for finding prey as well as used to get a three-dimensional image of the turtle’s
pond (Latta & Craig, 2009).
Red-bellied short-necked turtles, like other freshwater turtles have a nictitating
membrane (transparent third eyelid) for underwater vision. Their sense of smell is
achieved through the nose and through a specialized Jacobsen’s organ, which identifies
chemical debris floating in the air and water. Although turtles do not have an external
ear opening, they do have a tympanum (eardrum) that is covered with skin and can detect
low-frequency vibrations under water and on land.
Red-bellied short-necked turtles have four scent glands in the carapace. These glands
produce an odor as defense against predators and among competing males during breeding
season. They communicate with potential mates through extensive courtship ceremonies
that include the bobbing of their heads as they align their bodies (Legler and Georges,
1993).
- Other Communication Modes
- scent marks
- Perception Channels
- visual
- tactile
- acoustic
- echolocation
- vibrations
- chemical
Food Habits
Red-bellied short-necked turtles are omnivorous, feeding on filamentous algae, periphyton,
sponges, aquatic macrophytes, aquatic macro-invertebrates, terrestrial insects that
fall into the water, and carrion. These turtles also rely heavily on crushing mollusks,
fish, insects, worms, aquatic plants, vegetable matter and seeds as a part of daily
living (PNG Gas Project, 2005). They rely on their broad, sharp, horny jaws and front
feet to tear food, their tongue serves to direct food down the gullet. Many freshwater,
short-necked turtles, such as
Emydura subglobosa
and
Chelodina
species, ingest large quantities of water that contain their prey by gaping and sucking
in prey in the water (Legler & Georges, 2007).
The combination of an elongated digestive tract and slow passage rate ensures maximum
nutritional benefit from the large amounts of fiber ingested. Food intake is temperature
dependent; an increase in the ambient temperature will cause an increase in the heart
rate, in turn increasing the metabolism of the turtle, breaking down the food much
faster. Commensal bacteria and other microorganisms help with the task of breaking
down cellulose during its passage through the digestive tract. Fat is stored in the
abdomen so will not affect thermo-regulation.
Turtle malformations can exist due to diet restrictions, including disfigurement of
mouthparts caused by excessive keratin and megacephaly, a disorder where turtles,
eating and crushing hard food like mollusks, grow a severely enlarged head, up to
20% of the carapace length (Legler & Georges, 1993).
- Primary Diet
- omnivore
- Animal Foods
- fish
- carrion
- insects
- terrestrial non-insect arthropods
- mollusks
- terrestrial worms
- aquatic crustaceans
- Plant Foods
- leaves
- flowers
- algae
- macroalgae
- phytoplankton
Predation
Predators include introduced red foxes (
Vulpes vulpes
) and domestic cats (
Felis catus
). Water rats (
Hydromys chrysogaster
), goannas (
Varanus gouldii
),and crows (
Corvus tristis
) prey on nests of
Emydura macquarii
and may prey on
Emydura subglobosa
.
Much predation occurs in coastal areas, where predators include large marine turtles
(
Cheloniidae
), tiger sharks (
Galeocerdo cuvier
), crocodiles (
Crocodylus
species), and humans (Georges et al., 1993). Human predation includes taking of eggs
and adults as a local food source.
Emydura subglobosa
has four scent glands as a defense mechanism against predators. The odor usually
is only released when threatened. Although, the use of the musk is unknown, recent
data suggest that once the powerful odor is released, nearby predators leave the surrounding
area (Legler and Georges, 1993; Latta, 2009).
Ecosystem Roles
Red-bellied short-necked turtles feed on insects and plants. While digging in the
soil during egg-laying or while searching for food they allow for better aeration
of the soil by permitting nutrients to reinvigorate the soil, allowing for improved
water holding capacity (Georges, 2007). They serve as sustenance for local people
but also for large predators (Legler and Georges, 1993).
Commensal bacteria and other microorganisms, such as
Polystomoides australiensis
, live in bladders of
Emydura subglobosa
.
Notopronocephalus peekayi
live in the digestive tract of this species and other freshwater river turtles of
New Guinea. This species helps to break down cellulose (Alderton, 1988; Ferguson &
Smales, 2006).
- Ecosystem Impact
- creates habitat
- soil aeration
- commensal bacteria ( Polystomoides australiensis )
- commensal bacteria ( Notopronocephalus peekayi )
Economic Importance for Humans: Positive
The production of turtle meat and turtle products are important for cash economies
in New Guinea (Georges, 2007). Freshwater turtles and their eggs are an important
source of protein for some peoples (Rhoden and Genorupa, 2000).
Economic Importance for Humans: Negative
There are no known adverse effects of Emydura subglobosa on humans.
Conservation Status
Red-bellied short-necked turtles are listed as a species of least concern by the IUCN.
However, there may be isolated populations in arid regions throughout their range
and have extended times to sexual maturity. This combination leads some to believe
that a pre-emptive conservation program should be implemented (Martins and Souza,
2008; Georges 1995). Increasing anthropogenic threats also pose a threat (Rhodin and
Genorupa, 2000).
Additional Links
Contributors
Melissa Whistleman (author), Radford University, Karen Powers (editor), Radford University, Tanya Dewey (editor), University of Michigan-Ann Arbor.
- Australian
-
Living in Australia, New Zealand, Tasmania, New Guinea and associated islands.
- native range
-
the area in which the animal is naturally found, the region in which it is endemic.
- island endemic
-
animals that live only on an island or set of islands.
- temperate
-
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).
- terrestrial
-
Living on the ground.
- freshwater
-
mainly lives in water that is not salty.
- marsh
-
marshes are wetland areas often dominated by grasses and reeds.
- swamp
-
a wetland area that may be permanently or intermittently covered in water, often dominated by woody vegetation.
- riparian
-
Referring to something living or located adjacent to a waterbody (usually, but not always, a river or stream).
- ectothermic
-
animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature
- heterothermic
-
having a body temperature that fluctuates with that of the immediate environment; having no mechanism or a poorly developed mechanism for regulating internal body temperature.
- bilateral symmetry
-
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.
- indeterminate growth
-
Animals with indeterminate growth continue to grow throughout their lives.
- polygynandrous
-
the kind of polygamy in which a female pairs with several males, each of which also pairs with several different females.
- iteroparous
-
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).
- seasonal breeding
-
breeding is confined to a particular season
- sexual
-
reproduction that includes combining the genetic contribution of two individuals, a male and a female
- oviparous
-
reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.
- natatorial
-
specialized for swimming
- diurnal
-
- active during the day, 2. lasting for one day.
- motile
-
having the capacity to move from one place to another.
- sedentary
-
remains in the same area
- solitary
-
lives alone
- visual
-
uses sight to communicate
- tactile
-
uses touch to communicate
- chemical
-
uses smells or other chemicals to communicate
- scent marks
-
communicates by producing scents from special gland(s) and placing them on a surface whether others can smell or taste them
- visual
-
uses sight to communicate
- tactile
-
uses touch to communicate
- acoustic
-
uses sound to communicate
- echolocation
-
The process by which an animal locates itself with respect to other animals and objects by emitting sound waves and sensing the pattern of the reflected sound waves.
- vibrations
-
movements of a hard surface that are produced by animals as signals to others
- chemical
-
uses smells or other chemicals to communicate
- carrion
-
flesh of dead animals.
- macroalgae
-
seaweed. Algae that are large and photosynthetic.
- phytoplankton
-
photosynthetic or plant constituent of plankton; mainly unicellular algae. (Compare to zooplankton.)
- soil aeration
-
digs and breaks up soil so air and water can get in
- pet trade
-
the business of buying and selling animals for people to keep in their homes as pets.
- food
-
A substance that provides both nutrients and energy to a living thing.
- omnivore
-
an animal that mainly eats all kinds of things, including plants and animals
References
Adams, M., A. Georges. 1996. Electrophoretic Delineation of Species Boundaries Within the Short-Necked Freshwater Turtles of Australia. Zoological Journal of The Linnean Society , 118: 241-260.
Alderton, D. 1988. Turtles and Tortoises of the World . New York, N.Y: Facts on Files, Inc..
Bagatto, B., R. Henry. 1999. Aerial and Aquatic Respiration in the Snapping Turtle Chelydra Serpentina. Journal of Herpetology , 33/3: 490-492.
Burbidge, A., J. Kirsch, A. Main. 1974. Relationships Within the Chelidae (Testudines:Pleurodira of Australia and New Guinea). Copeia , 1974/2: 392-409.
Carr, A. 1952. Handbook of Turtles . Ithaca, New York: Cornell University Press.
Conant, R., J. Collins. 1998. A Field Guide to Reptiles and Amphibians- Eastern/Central North America . New York, NY: Houghton Mifflin Company.
Ellison, J. 2009. Wetlands of the Pacific Island Region. Wetlands of the Pacific Island Region , 17/3: 169-206.
Ernst, C., R. Barbour. 1989. Turtles of the World . USA: Smithsonian Institution.
Ferguson, M., L. Smales. 2006. Helminth Assemblages of the Turtle Emydura macquarii (Pleurodira: Chelidae) Queensland, Australia. Journal of Parasitology , 92(1): 186-188.
Georges, A., E. Alacs, M. Pauza, F. Kinginapi, A. Ona, C. Eisemberg. 2008. Freshwater Turtles of the Kikori Drainage, Papua New Guinea, with Special Reference to the Pig-Nosed Turtle, Caretiochelys Insculpta. Wildlife Research , 35/7: 700-711.
Georges, A., F. Guarino, B. Bito. 2006. Freshwater Turtles of the TransFly Region of Papua New Guinea-Notes on Diversity, Distribution, Reproduction, Harvest and Trade. Wildlife Research , 33/5: 373.
Georges, A., C. Limpus, J. Parmenter. 1993. Natural History of Chelonia. Fauna of Australia , 2A: 1-18.
Georges, A. 2007. Freshwater Turtles of the Kikori. Applied Ecology , 1: 1-46.
Georges, A. 1995. Setting Conservation Priorities for Australian Freshwater Turtles. Herpetology in Australia-A Diverse Discipline , 1/1: 49-58.
Iverson, J., S. Thomson, A. Georges. 2001. Validity of Taxonomic Changes for Turtles Proposed by Wells and Wellington. Journal of Herpetology , 35/3: 361-368.
Latta, C. 2009. Caring for Australian Freshwater Turtles In Captivity. Australian Freshwater Turtle Forum , 1: 1-5.
Legler, J., A. Georges. 1993. Family Chelidae. Fauna of Australia , 2/1: 142-152.
Martins, F., F. Souza. 2008. Estimates of Growth of The Atlantic Rain Forest Freshwater Turtle Hydromedusa Maximiliani (Chelidae). Journal of Herpetology , 42(1): 54-60.
Norris, J. 1996. Male Courtship in the New Guinean Turtle, Emydura Subglobosa(Pleurodia, Chelidae). Journal of herpetology , 30/1: 78-80.
Pearse, D., J. Avise. 2001. Turtle Mating Systems: Behavior, Sperm Storage, and Genetic Paternity. Journal of Heredity , 92/2: 206-211.
Rhodin, A., V. Genorupa. 2000. Conservation Status of Freshwater Turtles in Papua New Guinea. Asian Turtle Trade , 1: 130-36.
Scheyer, T., B. Brullmann, M. Sanchez-Villagra. 2008. The Ontogeny of the Shell In the Side-necked Turtles, With Emphasis On the Homologies of Costal and Neural Bones. Journal of Morphology , 269/8: 1008-1021.
Thomson, S. 2003. "Distinguishing The Yellow Face Turtle and the Diamond Head Turtle" (On-line). Accessed March 05, 2010 at http://www.chelonia.org/Articles/emydurakey.htm .
Webb, G. 1978. Observations on Basking in Some Australian Turtles (Reptilia:Testudines:Chelidae). Herpetologica , 34/1: 39-42.
Werneburg, I., J. Hugi, J. Muller, M. Sanchez-Villagra. 2009. Embryogenesis and Ossification of Emydura Subglobosa and Patterns of Turtle Development. Developmental Dynamics , 238/11: 2770-2786.
de Magalhaes, J., J. Costa. 2009. "AnAge database" (On-line). Accessed April 20, 2010 at http://genomics.senescence.info/species/query.php?search=emydura .
Enesar Consulting Pty Ltd. 2005. Environmental Impact Statement. PNG Gas Project , 1: 1-16.