The long-nosed echidna is endemic to New Guinea (Gregory, 1997).
Long-nosed echidnas primarily inhabitate mountain forests, although some live on highly elevated alpine meadows. The species does not live along the coastal plains (Augee, 1993; Walker, 1991).
As monotremes, the long-nosed echidnas possess one body cavity for the external openings of their urinary, digestive, and reproductive organs. The species has a very short tail relative to its average body length of 450-775 mm. The core body is covered in course brown or black hair that often hides the spines covering the back. Zaglossus has a pronounced downcurved snout, which accounts for two-thirds of the length of its head. Lack of teeth in the species is compensated by rows of spikes/horny teeth-like projections on the enormous tongues of the animals. Long-nosed echidnas generally have clawed feet, the front ones important in digging for food. Within the species there is variation in the number of clawed digits on each foot. Many have claws only on the middle three of the five digits present; others have claws on each digit. The males of the species can be distinguished from the females by the presence of a spur on the inner surface of each hind leg near the foot. (Augee, 1993; Gregory, 1997; Griffiths, 1968; Walker, 1991).
Little is known about reproduction in Zaglossus, although they are believed to be similar in reproductive pattern to their sister species, the short-nosed echidna (Tachyglossus aculeatus). Frequency of breeding, courtship rituals, and possible male parental care are unknown for both echidna species. It is thought that the breeding season for the long-nosed echidna is in July. A captivespecimen lived for a record 30 years and 8 months.
(Gregory, 1997; Walker, 1991).
As with reproductive aspects of the biology of long-nosed echidnas, their behavior and social systems are largely unknown. They are believed to be solitary. Research on their sister species has shown that the echidna's behavior is characteristically simpler than that of most mammals. The short-nosed echidnas display no evidence of grooming, aggression, courting, or maternal behaviors (Walker, 1991).
The diet ofconsists almost exclusively of earthworms. When earthworms are eaten, they are positioned by the echidna to go front first into the snout. The powerful tongue of the long-nosed echidna protrudes a small distance and wraps around the front of the worm. While the worm is pulled into the mouth, the echidna's tongue holds the worm in place with its spikes. Termites and other insect larvae are also eaten, they may eat ants.
(Augee, 1993; Walker, 1991)
The meat of Zaglossus is a popular food source in New Guinea (Augee, 1993; Walker, 1991).
Long-nosed echidnas can destroy gardens with their burrowing. In fact, this is seldom a problem. (Gregory, 1997)
Listed in appendix II of CITES,is categorized as vulnerable by IUCN. Hunting with trained dogs by the New Guinean people as well as loss of natural forest habitat due to farming are the primary causes for the species' endangerment. Data tabulated in 1982 indicated that only 1.6 Zaglossus existed per square kilometer of suitable habitat. If the data were accurate, about 300,000 long-nosed echidnas were in existence then, and the number has dropped since that time (Walker, 1991).
The long-nosed echidna is reported to have sweat glands spread over its entire body surface.
Pleistocene fossils of Zaglossus have been found throughout Australia and Tasmania. No other member of the genus currently occurs outside of New Guinea. It is thought that the disappearance of long-nosed echidnas in Australia was due to climate changes that led to decreased presence of earthworms.
In the past, taxonomists recognized up to four species of Zaglossus. At present all long-nosed echidnas are considered to be one species,(Augee, 1993; Walker, 1991).
Danielle Cross (author), University of Michigan-Ann Arbor.
Living in Australia, New Zealand, Tasmania, New Guinea and associated islands.
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.
uses smells or other chemicals to communicate
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.
having the capacity to move from one place to another.
This terrestrial biome includes summits of high mountains, either without vegetation or covered by low, tundra-like vegetation.
the area in which the animal is naturally found, the region in which it is endemic.
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.
reproduction that includes combining the genetic contribution of two individuals, a male and a female
uses touch to communicate
Augee, M. L. 1993. Echidnas of Australia and New Guinea. New South Wales University Press, Australia.
Gregory, Cal. 1997. http://www.omen.com.au/-echidna/index.htm
Griffiths, Mervyn. 1968. Echidnas. Pergamon Press, New York.
Nowak, R. M. 1991. Walker's Mammals of the World. Fifth Edition. Johns Hopkins University Press, Baltimore.