Geographic Range
Macropus dorsalis
(black-striped wallaby) is a marsupial that makes its home in Australia. Historically,
M. dorsalis
was widespread throughout New South Wales and Queensland. Due to the destruction
of their habitat, the current range for
M. dorsalis
is now confined to a small part of northern New South Wales and areas of Queensland.
- Biogeographic Regions
- australian
Habitat
Macropus dorsalis
prefers warm, wet summers and dry winters. These wallabies can usually be found
in dense areas of vegetation. These areas include dense rainforests, forests with
a substantial under story, and areas of regrown brigalow scrub, which provide shelter
during the day. Many times, they will be found on the edge of these dense vegetation
areas, where they can migrate out into the pastures at night to feed.
- Habitat Regions
- temperate
- tropical
- terrestrial
- Terrestrial Biomes
- forest
- rainforest
- scrub forest
- Other Habitat Features
- agricultural
Physical Description
Macropus dorsalis
gets its common name, black-striped wallaby, from the black stripe that runs along
the middle of its back. The head and body stand from 100 cm to 159 cm in height,
with the tail being 54 to 83 cm in length. Like other members of the
Macropodidae
, the length of the tail is an adaptation that allows them to balance both when moving
and sitting still. The hind legs also tend to be larger and stronger than the front
legs, allowing these animals to use a jumping motion for movement. Adult males tend
to be three times larger than adult females.
- Other Physical Features
- endothermic
- bilateral symmetry
- Sexual Dimorphism
- male larger
Reproduction
Details on the mating habits of
M. dorsalis
are not available in the literature. However, other species in the genus
Macropus
are polygynous. Males compete for access to females. This competition can become
very intense, with injuries occuring to the competitors in the interaction. There
have been accounts of females also being injured when males are overly aggressive
in pursuing them. Generally, the dominant male in a social group will be the one
to mate with the females. Because of the extreme sexual dimorphism in
M. dorsalis
, it is likely that the mating system of this species is similar.
- Mating System
- polygynous
The general reproductive behavior of the genus
Macropus
is interesting in several respects. Like all members of the order Diprododontia,
these animals lack a placenta, and so are unable to efficiently provide nutrients
and oxygen to a large fetus. They therefore give birth to very altricial young, which
are then nursed in a pouch, where they complete their development.
Females in
Macropus
are reported to be polyestrus. The estrus cycle of most members of the genus is
between 28 and 45 days in length. Females may be receptive to males only for a breif
time during this cycle. Females of species which have been studied undergo a postpartum
estrus, within two days of parturition, and typically conceive at that time.
The breeding season of this species has not been reported. In captivity, births of
M. dorsalis
have been recorded as occuring in March, September, and October. When a female is
not nursing a joey, gestation is short in the genus, ranging from 33 to 35 days. However,
the embryo undergoes a diapause if the mother is nursing another offspring when conception
occurs. Embryonic dispause happens after the egg is fertilized and the embryo begins
to develop, but the development is arrested at around the 70 to 100 cell stage. Because
of the short gestation and the need for an empty pouch in which to nurse and incubate
a newborn joey, this diapause is highly adaptive. After the first joey leaves the
mother's pouch for good, then the embryo in the mother resumes the process of development.
Because of embryonic diapause, a mother can rapidly produce a new offspring, should
her first joey fail to survive the harsh Australian environment.
Although details are not available for
M. dorsalis
, other members of the genus weigh less than one gram at birth (
Macropus rufus
weighs 0.75 g). and it is likely that
M. dorsalis
neonates are comparably small. The newborn makes its way by squirming from the birth
canal to the opening of the pouch, which it enters. Once in the pouch, the young
attaches to a nipple. In
M. rufus
, the young does not let go of the nipple until it is 70 days old, and does not stick
its head out of the pouch until it is 150 days old. It may begin to leave the pouch
for short intervals by the age of 190 days, and may permanently leave the pouch by
about 235 days of age. Within
Macropus
development seems to take about the same amount of time, despite differences in final
adult size, so it is likely that these events are similarly timed in
M. dorsalis
. Weaning occurs in
M. dorsalis
between 10 and 12 months of age, and the young become more or less independent at
that time. The average age of independence is reported to be 300 days of age.
Males are sexually mature at the age of 20 months, whereas females are sexually mature
as young as 14 months.
- Key Reproductive Features
- iteroparous
- gonochoric/gonochoristic/dioecious (sexes separate)
- sexual
- fertilization
- viviparous
- embryonic diapause
- post-partum estrous
Parentla investment in this species has not been documented. However, in
Macropus
, a great deal is known. After the gestation period, the joey soon finds its way into
the mother's pouch where it begins the development process. The mother feeds the
joey with her milk while the joey is still confined to the mother's pouch. After
5 to 6 months the joey may begin to leave the pouch for short periods of time, always
returning to the mothers pouch. A joey will then begin to spend 1-2 hours a day out
of the mother's pouch, and begin feeding on grass four times a day at the age of around
7 months. The joey becomes increasingly independent and spends more time out of the
pouch, relies less on the mother for milk, and finally becomes independent by about
a year of age. Males have no role in parental care.
- Parental Investment
- altricial
-
pre-fertilization
-
protecting
- female
-
protecting
-
pre-hatching/birth
-
provisioning
- female
-
protecting
- female
-
provisioning
-
pre-weaning/fledging
-
provisioning
- female
-
protecting
- female
-
provisioning
-
pre-independence
-
provisioning
- female
-
protecting
- female
-
provisioning
Lifespan/Longevity
The lifespan of
M. dorsalis
has not been reported, but information on the genus
Macropus
reveals that they can live to be 20 years of age in captivity, but may only survive
to be 10 years of age in the wild. It is likely that this species is similar to other
members of the genus.
Behavior
Black-striped wallabies generally live in groups of from 2 to 20 animals. Most of
the feeding is done in groups. Animals typically remain within 30 meters of each
other during feeding times. This closeness allows for communication in the dense
vegetation, where sounds would be hard to hear from a distance farther than 30 meters.
Black-striped wallabies stay withing closer proximity of other group members than
do other macropods, which live in open areas and do not have vegetation to block the
sound.
Macropus dorsalis
has open-membership groups. This means that group membership changes over time,
and individuals do not always maintain the same associations. Groups size also varies
over time.
Macropus dorsalis sleeps during the day and feeds during the night, making them primarily nocturnal.
Locomotion in macropods is unique among mammals. When moving rapidly, these animals
hop using only their hind legs, keeping their tails extended behind them for balance.
However, when moving slowly, macropods use all four feet and their tails in locomotion.
Young joeys are known to box playfully, but the same behavior in adult males is serious
business. Adult males box to determine who dominance ranking within the group. Dominance
rank influences mating prospects.
- Key Behaviors
- terricolous
- saltatorial
- nocturnal
- motile
- social
- dominance hierarchies
Home Range
The size of the home range in this species has not been reported.
Communication and Perception
Information on communication in this species is scant.
M. dorsalis
uses vocal communication to maintain contact between individuals when groups are
in thick underbrush. Some members of the genus
Macropus
will growl to alarm predators.
Other forms of communication also play some role in this species. Tactile communication
is used in the boxing play of young joeys, as well as in the sparring of adults.
It probably also occurs during mating, and it definitely happens between a mother
wallaby and her joey. Visual signals such as body postures are probably also important
in aggressive encounters, although because of the dense vegetation in the habitat
of this species, it can be assumed that visual signals are not used over long distances.
Food Habits
Black-striped wallabies feed mainly on monocot grasses, but also browse on forbs
and other shrubs. They have the ability to change diet to eat more shrubs when there
is less grass available in the winter. They prefer the soft, leafy part of the plant.
M. dorsalis
generally feeds during the night in either pastures or open fields.
- Plant Foods
- leaves
- wood, bark, or stems
- seeds, grains, and nuts
Predation
Humans are one of the main predators of
M. dorsalis
. Ranchers receive permits to hunt them on their land. The goal of the ranchers is
to elimate
M. dorsalis
from their land, beause these wallabies damage crops and pastures. It is also likely
that dingos prey upon this species.
Ecosystem Roles
Macropus dorsalis
is an important disperser of seeds. Seeds of monocots upon which
M. dorsalis
feeds have a higher chance of germination if they have gone through the digestive
system of
M. dorsalis
. Wallabies also help replenish nutrients to the area through their feces. To the
extent that this species serves as prey, they affect predator populations.
- Ecosystem Impact
- disperses seeds
Economic Importance for Humans: Positive
Macropus dorsalis
has not been reported to have any particular positive impact on human economies.
However, the genus
Macropus
is an important animal in zoos across the world. Also, there may be some ecotourism
related to these animals, as foreign visitors to Australia like to see macropods in
their natural habitat.
- Positive Impacts
- ecotourism
Economic Importance for Humans: Negative
Macropus dorsalis
is considered to be a pest. Ranchers have long believed that
M. dorsalis
has caused the depletion of grass in their pastures. Even though studies have shown
that cattle are the main cause of the depletion of grasses in the pastures, the Queensland
Parks and Wildlife Service allows ranchers to hunt wallabies on their land. Ranchers
have also cleared areas of brush, destroying areas for the wallabies to take shelter
during the day.
- Negative Impacts
- crop pest
Conservation Status
The loss of
M. dorsalis
has been of some concern in Australia. Much of the land that used to be covered
in dense forest has now been cleared for agricultural fields and pastures. This has
caused a decline in both the range and population size of
M. dorsalis
. Management is the key to the survival of black-striped wallabies. Dense forested
areas need to be maintained and restored to ensure their survival. Also, allowing
the ranchers to hunt them during the dry season when grass is not as abundant would
have a smaller impact on the populations than the current hunting regime.
Other Comments
Macropus dorsalis
is a species that has been studied very little, and more biological studies need
to be done on the species to get a better understanding of how these animals fit into
the ecosystem. This would allow biologists to better manage the population of back-striped
wallabies in the future.
Additional Links
Contributors
Nancy Shefferly (editor), Animal Diversity Web.
Todd Jewell (author), University of Wisconsin-Stevens Point, Chris Yahnke (editor, instructor), University of Wisconsin-Stevens Point.
- 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.
- 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).
- tropical
-
the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.
- terrestrial
-
Living on the ground.
- forest
-
forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.
- rainforest
-
rainforests, both temperate and tropical, are dominated by trees often forming a closed canopy with little light reaching the ground. Epiphytes and climbing plants are also abundant. Precipitation is typically not limiting, but may be somewhat seasonal.
- scrub forest
-
scrub forests develop in areas that experience dry seasons.
- agricultural
-
living in landscapes dominated by human agriculture.
- polygynous
-
having more than one female as a mate at one time
- 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).
- sexual
-
reproduction that includes combining the genetic contribution of two individuals, a male and a female
- fertilization
-
union of egg and spermatozoan
- viviparous
-
reproduction in which fertilization and development take place within the female body and the developing embryo derives nourishment from the female.
- embryonic diapause
-
At about the time a female gives birth (e.g. in most kangaroo species), she also becomes receptive and mates. Embryos produced at this mating develop only as far as a hollow ball of cells (the blastocyst) and then become quiescent, entering a state of suspended animation or embryonic diapause. The hormonal signal (prolactin) which blocks further development of the blastocyst is produced in response to the sucking stimulus from the young in the pouch. When sucking decreases as the young begins to eat other food and to leave the pouch, or if the young is lost from the pouch, the quiescent blastocyst resumes development, the embryo is born, and the cycle begins again. (Macdonald 1984)
- altricial
-
young are born in a relatively underdeveloped state; they are unable to feed or care for themselves or locomote independently for a period of time after birth/hatching. In birds, naked and helpless after hatching.
- saltatorial
-
specialized for leaping or bounding locomotion; jumps or hops.
- nocturnal
-
active during the night
- motile
-
having the capacity to move from one place to another.
- social
-
associates with others of its species; forms social groups.
- dominance hierarchies
-
ranking system or pecking order among members of a long-term social group, where dominance status affects access to resources or mates
- visual
-
uses sight to communicate
- tactile
-
uses touch to communicate
- acoustic
-
uses sound to communicate
- visual
-
uses sight to communicate
- tactile
-
uses touch to communicate
- acoustic
-
uses sound to communicate
- chemical
-
uses smells or other chemicals to communicate
- ecotourism
-
humans benefit economically by promoting tourism that focuses on the appreciation of natural areas or animals. Ecotourism implies that there are existing programs that profit from the appreciation of natural areas or animals.
- herbivore
-
An animal that eats mainly plants or parts of plants.
- folivore
-
an animal that mainly eats leaves.
- endothermic
-
animals that use metabolically generated heat to regulate body temperature independently of ambient temperature. Endothermy is a synapomorphy of the Mammalia, although it may have arisen in a (now extinct) synapsid ancestor; the fossil record does not distinguish these possibilities. Convergent in birds.
- 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.
References
Baxter, G., E. Moll, A. Lisle. 2001. Pasture grazing by black-striped wallabies (*Macropus dorsalis*) in central Queensland. Wildlife Research , 28: 269-276.
Evans, M., P. Jarman. 1999. Diets and feeding selectivities of bridled nailtail wallabies and black-striped wallabies. Wildlife Research , 26: 1-19.
Feldhamer, G., L. Drickamer, S. Vessey, J. Merritt. 1999. Mammalogy: Adaptatation, Diversity, and Ecology . USA: McGraw Hill.
Hand, S. 1989. Care and Handling of Australian Native Animals . Australia: Surrey Beatty & Sons Pty Limited.
Hoolihan, D., A. Goldizen. 1998. The grouping dynamics of the black-striped wallaby. Wildlife Research , 25: 467-473.
Jarman, P. 1994. The eating of seedheads by species of Macropodidae. Australian Mammalogy , 17: 51-63.
Nowak, R. 1999. Walker's Mammals of the World, Sixth Edition . Baltimore and London: The Johns Hopkins University Press.
Noah's Ark Wildlife Coalition, Inc. 2002. "Guide To Caring For Australian Animals" (On-line). Noah's Ark Wildlife Coalition. Accessed June 22, 2004 at http://www.noahsark.org.au/?act=wildlife&file=macropodsinfo#can5 .
Kangaroo Conservation Center. 2002. "Western Grey Roos" (On-line ). Kangaroo Conservation Center. Accessed 12-03-02 at http://www.kangaroocenter.com/westerngrey.html .