Geographic Range
Chelodina longicollis
is endemic to Australia, and its geographic range extends from the Wilton River in
eastern Queensland to the Murray River, along the south western border of New South
Wales. Its geographic range includes the entire Murray-Darling Basin.
- Biogeographic Regions
- australian
- Other Geographic Terms
- island endemic
Habitat
Common snake-necked turtles are semi-aquatic. Although they prefer the slow moving
waters of swamps or wetlands, they can also be found in streams and rivers. In aquatic
environments, they are primarily bottom dwelling, but occasionally leave the water
to bask in the sun. If conditions are dry, they seek out new habitat. Some individuals
seek extended refuge and may estivate until flood waters return. Estivation usually
occurs under trees in forested habitats where they can burrow into fallen foliage
on the forest floor near shrubs and logs. Common snake-necked turtles are usually
the only
turtle
species in their immediate environment.
- Habitat Regions
- temperate
- terrestrial
- freshwater
- Terrestrial Biomes
- forest
- Aquatic Biomes
- lakes and ponds
- rivers and streams
- temporary pools
- Wetlands
- swamp
Physical Description
Common snake-necked turtles are medium-sized
turtles
, with an average length of 25 cm. They have a black to light brown oval carapace
that contains a shallow central groove. The plastron is cream colored with dark seams.
Their necks are long and narrow, with a brown to gray dorsal surface and a yellow
ventral surface. On average, the neck is approximately 60% of the plastron length
and is covered with short tubercles. The head is small and pointed and the limbs are
dark grey to brown. Sexual dimorphism in this species is subtle. When compared to
males, females are larger, have deeper shells and have a shorter, fatter tail that
is hidden. Males have longer, thicker tails than females and a concave plastron. These
distinctions are subtle which makes gender determination difficult. Juveniles tend
to be black to dark gray with an orange stripe down either side of the neck and jaw.
They also have orange spots on the plastron.
- Other Physical Features
- ectothermic
- heterothermic
- bilateral symmetry
- Sexual Dimorphism
- female larger
- sexes shaped differently
Development
There is little information about the development of
Chelodina longicollis
. Adult females lay their eggs near water's edge, and embryo estivation occurs as
the eggs develop. Sex determination is not based on incubation temperatures, which
is unlike that of most
chelonian
turtles.
Reproduction
Chelodina longicollis
is polygynandrous, and during breeding season, males become more active and travel
longer distances, which increases their their potential number of matings. Females
increase movement during nesting periods to find optimal nesting sites. Males engage
in head bobbing and cloacal touching during the mating sequence and attempt to align
barbels with those of females. In preparation for copulation, which occurs in the
water, males mount females from the rear and align their plastron over the females
carapace. Occasionally, females struggle free of their mate but males rarely retreat.
Copulation occurs while the male and female plastrons are directly adjacent from one
another.
Chelodina longicollis
lacks many of the complex mating behaviors present in other species and freely mates
with
Chelodina canni
; however these two species are rarely sympatric and thus, hybridization rarely occurs.
- Mating System
- polygynandrous (promiscuous)
Common snake-necked turtles breed once annually, from September to October. Nesting
occurs during late spring and early summer, from October to December. Females lay
8 to 24 hard-shelled, ellipsoid eggs in nests close to water. Eggs are approximately
20 mm wide and 30 mm long and weigh between 6 and 7 g. Typically, females lay three
clutches per year are all eggs are laid. Embryo estivation occurs during development,
with incubation lasting between 120 to 150 days. Young emerge during autumn, from
January to late April. Common snake-necked turtles are slow to mature, and most males
reach sexual maturity between 7 and 8 years of age. Females reach sexual maturity
between 10 and 12 years of age. Male-female birth ratio is approximately 1 to 1. Reproductive
success is greater for swamp populations than for residents of permanent lakes, as
their is significantly less competition for resources in wetland habitats
- Key Reproductive Features
- iteroparous
- seasonal breeding
- gonochoric/gonochoristic/dioecious (sexes separate)
- sexual
- oviparous
Prior to laying their eggs,
Chelodina longicollis
females search for optimal nesting sites and may travel more than 500 m from water
to find nesting sites on elevated landscape structures (e.g., crests or ridges). Nesting
can occur in a variety of substrates, from soft sand to hard clay, and has even been
documented on gravel roads. Prior to excavating the nest, which is simply a large
hole for which females to lay their eggs in, females eject large volumes of cloacal
fluid on the nest site, which helps soften the ground. Females excavate the nest with
their hind claws and may return to the nearest source of water multiple times to take
on more water to soften the earth for excavation. Once eggs have been laid, excavated
substrate is placed back into the hole with her rear claws. The female then compacts
the loose soil by raising her body and suddenly collapsing on top of the nest. There
is no information available on paternal care in this species.
- Parental Investment
- no parental involvement
Lifespan/Longevity
The average life span of
Chelodina longicollis
ranges from 31 to 37 years. The lifespan of wild and captive individuals appears
to be approximately equal; however, very few have been held in captivity. During dry
periods,
C. longicollis
moves to more permanent bodies of water (e.g. lakes), where resource competition
is high. As a result, many individuals die and thus, longevity tends to be higher
in wetland habitats than in permanent lake. Females are able to withstand these pressures
better than males because of their larger size.
Behavior
Common snake-necked turtles frequently change habitats. During breeding seasons, males
and females are known to increase movements and environmental conditions (e.g., rainfall
and moisture levels) can have an impact on local densities of common snake-necked
turtles. They are known to move great distances to find a suitable habitat. Although
many individuals can live in the same wetland, they are generally thought of as solitary
and move independently of one another. Common snake-necked turtles have good water
storage capabilities, which allows them to lie dormant or estivate for extended periods
of time.
Home Range
Chelodina longicollis
has a large home range, which increases as distance between wetlands increases. Evidence
suggests that movement depends on rainfall amounts. As annual rainfall decreases,
movement tends to increase, and some individuals have been recorded to move up to
5.2 km. Distances between wetlands or permanent waters vary, and many individuals
associate with more than one wetland over the course of several years. High rates
of movement were recorded when wetland distances were no more than 1.2 km. On average,
adult males move the greatest distance, while juveniles move the least.
Communication and Perception
Chelodina longicollis
is primarily solitary; however, communication between conspecifics usually occurs
via touching or the release of pheromones. Individuals emit a pungent musk to deter
predators. During mating, males perform head bobbing and fast swimming in an attempt
to gain the attention of females.
Chelodina longicollis
perceives the immediate environment through visual, haptic, and olfactory stimulation.
- Other Communication Modes
- scent marks
Food Habits
Chelodina longicollis
is carnivorous and is an ambush predator. Primary prey includes aquatic invertebrates,
fish,
tadpoles
,
crustaceans
, plankton and carrion. Occasionally, they prey upon terrestrial insects. Intraspecific
competition has been known force movements between habitats. Prey are caught by the
use of a strike and gape action, and are sucked into the turtle’s mouth by a vacuum
that is created by the sudden lowering of the hyoid bone. When food resources are
limited,
C. longicollis
preys upon a large variety of small organisms.
- Primary Diet
-
carnivore
- piscivore
- insectivore
- eats non-insect arthropods
- scavenger
- Animal Foods
- fish
- carrion
- insects
- terrestrial non-insect arthropods
- other marine invertebrates
- zooplankton
Predation
Predators of common snake-necked turtles include
red foxes
,
water rats
,
goannas
,
Australian ravens
,
white-breasted sea eagles
and
dingos
. When fox predation is high, populations tend to be dominated by adults, as foxes
primarily prey upon juveniles and eggs. To deter predators, common snake-necked turtles
emit a foul-smelling musk, or yellow fluid from their musk glands. When threatened,
individuals tuck their head into their shell and lean into the threatening organism
with their shell. The also perform defensive snapping when threatened.
Ecosystem Roles
Chelodina longicollis
feeds on aquatic invertebrates, fish,
tadpoles
,
crustaceans
, and plankton. It is also a major prey item for
Vulpes vulpes
, which is not native to Australia. There is no information available on parasites
of this species.
Economic Importance for Humans: Positive
The common snake-necked turtle is commonly hunted by indigenous Australians for their
meat. They are also studied as biological indicators of wetland habitat quality.
- Positive Impacts
- food
- research and education
Economic Importance for Humans: Negative
There are no known adverse effects of Chelodina longicollis on humans.
Conservation Status
Chelodina longicollis
is not listed on the IUCN Red List of Threatened Species and is thought to be a species
of least concern. Important potential threats include habitat change, climate change,
and nest predation by invasive
red foxes
. This species is currently protected under state and federal legislation in Australia;
however, specific conservation measures are not high priority. Currently, they are
widespread and abundant throughout their geographic range.
Additional Links
Contributors
Monique Jarrett (author), University of Alberta, Augustana Campus, Doris Audet (editor), University of Alberta, Augustana Campus, John Berini (editor), Animal Diversity Web Staff.
- 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.
- forest
-
forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.
- swamp
-
a wetland area that may be permanently or intermittently covered in water, often dominated by woody vegetation.
- 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.
- 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.
- motile
-
having the capacity to move from one place to another.
- migratory
-
makes seasonal movements between breeding and wintering grounds
- 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
- chemical
-
uses smells or other chemicals to communicate
- carrion
-
flesh of dead animals.
- zooplankton
-
animal constituent of plankton; mainly small crustaceans and fish larvae. (Compare to phytoplankton.)
- food
-
A substance that provides both nutrients and energy to a living thing.
- carnivore
-
an animal that mainly eats meat
- piscivore
-
an animal that mainly eats fish
- insectivore
-
An animal that eats mainly insects or spiders.
- scavenger
-
an animal that mainly eats dead animals
References
Ernst, C., R. Barbour. 1989. Turtles of the World . Washington D.C.: Smithsonisn Institution Press.
Georges, A. 1988. Sex Determination Is Independent of Incubation Temperature in Another Chelid Turtle, Chelodina longicollis. Copeia , 1988: 248-254.
Kennett, R., J. Roe, K. Hodges, A. Georges. 2009. Chelodina longicollis (Shaw 1794) – Eastern Long-Necked Turtle, Common Long-Necked Turtle, Common Snake-Necked Turtle. Conservation Biology of Freshwater Turtles and Tortoises , 31: 1-8.
Kennett, R., A. Georges. 1990. HABITAT UTILIZATION AND ITS RELATIONSHIP TO GROWTH AND REPRODUCTION OF THE EASTERN LONG-NECKED TURTLE, CHELODINA LONGICOLLIS (TESTUDINATA: CHELIDAE), FROM AUSTRALIA. Herpetologica , 46/1: 22-33.
Murphy, J., W. Lamoreaux. 1978. Mating Behavior in Three Australian Chelid Turtles (Testudines: Pleurodira: Chelidae). Herpetologica , 34: 398-405.
Parker, L. Chelodina longicollis. Accessed November 12, 2010 at http://www.jcu.edu.au/school/tbiol/zoology/herp/Chelodinalongicollis.PDF .
Pearse, D., J. Avise. 2000. Turtle Mating Systems: Behavior, Sperm Storage and Genetic Paternity. Journal of Heredity , 2: 206-211.
Roe, J., A. Brinton, A. Georges. 2009. Temporal and spatial variation in landscape connectivity for a freshwater tur tle in a temporally dynamic wetland system. Ecological Applications , 19/5: 1288 –1299.
Roe, J., A. Georges. 2008. MAINTENANCE OF VARIABLE RESPONSES FOR COPING WITH WETLAND DRYING IN FRESHWATER TURTLES. Ecology , 89/2: 485-494.
Roe, J., A. Georges. 2008. Terrestrial activity, movements and spatial ecology of an Australian freshwater turtle, Chelodina longicollis, in a temporally dynamic wetland system. Austral Ecology , 33: 1045–1056.
Thompson, M. 1983. Populations of the Murray River Tortoise, Emydura (Chelodina): the Effect of Egg Predation by the Red Fox, Vulpes vulpes. Australian Wildlife Res. , 10: 363-371.
2003. Australo-American sideneck turtles. Pp. 77-83 in Grzimek's Animal Life Encyclopedia , Vol. 7, 2 Edition. Farmington Hills: Gale Group.