Overview

Distribution

Lumholtz’s tree kangaroos, Dendrolagus lumholtzi, inhabit an area of approximately 5,500 sq. km in Northeast Queensland, Australia. Their range extends from the Daintree River (northern limit) to the southern end of Cardwell Range (southern limit), west to the rainforest/wet sclerophyll forest interface, and east to the coast. Their greatest concentration is in the fragmented forests of the Atherton tablelands. While possibly occurring sympatrically with Bennett’s tree kangaroos in the Mt. Carbine Tableland, the two species are generally considered allopatric. Dendrolagus lumholtzi is often found in remnant and secondary rainforests on basalt soils. It is a non-migratory species, and is only found in its native range. An estimated 12% of its distribution is within national parks; there is also considerable overlap with a World Heritage Area.

Biogeographic Regions: australian (Native )

  • Flannery, T., R. Martin, A. Szalay. 1996. Tree Kangaroos - A Curious Natural History. Melbourne: Reed Books Australia.
  • Newell, G. 1999. Australia’s tree-kangaroos: current issues in their conservation. Biological Conservation, 87/1: 1-12.
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Range Description

This species is present in the rainforests between Ingham and Mossman in north-eastern Queensland, Australia. It is now largely restricted to upland rainforests because of extensive clearing of lowland rainforests. Its area of occupancy has declined substantially in upland areas because of clearing of prime habitat on basalt soils on the Atherton Tableland (Maxwell et al. 1996). The elevational range is sea level to 1,600 m asl.
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Physical Description

Morphology

Dendrolagus lumholtzi is a small macropodid, with males averaging 8.6 kg and females averaging 7.1 kg. Adults have an average head and body length of 0.5 m, and an average tail length of 0.7 m. The hindlimbs are well developed but proportionally smaller than those of terrestrial kangaroos. The tail and forelimbs, on the other hand, are proportionally larger than those of terrestrial kangaroos. These are adaptations for arboreal locomotion. The tail is hairy, uniformly thick, non-prehensile, and may be up to 15% longer than the combined head-body length. The arms are well-developed and muscular. Ears are short and ursine. Long, curved claws are present on all five digits of the forepaws. The hind paws include a large fourth digit and medium fifth digit; the first and second digits are syndactylous, but with 2 claws. No hallux is present. Both the fore and hind paws have large, fleshy pads with numerous tuberculations (papillae), used for gripping arboreal surfaces. The entire body is covered in hair: back hair is grizzled gray with blackish tips and the underbelly is creamy or sometimes orange. The muzzle is black and there is a distinctive pale gray forehead band. The forepaws, hindpaws, and tip of the tail are also black. The adult tail is bicolored: the lower surface is black, and the upper surface is gray (same color as the back). Juveniles have an all-black tail and lack the pale forehead band. There is no evidence of significant sexual dimorphism, seasonal variation, geographic variation, or subspecies. Dendrolagus lumholtzi has long, blade-like upper premolars, similar to that of Dendrolagus inustus; this is thought to be ancestral among tree kangaroos. While the basal metabolic rate is not known precisely, it is thought to be low for a mammal of its size.

Average mass: 8.6 (males), 7.1 (females) kg.

Average length: 0.5 m.

Other Physical Features: endothermic ; homoiothermic; bilateral symmetry

Sexual Dimorphism: male larger

  • Procter-Gray, E. 1985. The Behavior and Ecology of Lumholtz's Tree-Kangaroo, Dendrolagus lumholtzi (Marsupialia: Macropodidae). Cambridge: Harvard University.
  • Procter-Gray, E., U. Ganslosser. 1986. The Individual Behaviors of Lumholtz's Tree-Kangaroo: Repertoire and Taxonomic Implications. Journal of Mammology, 67/2: 343-352.
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Ecology

Habitat

Dendrolagus lumholtzi inhabits upland rainforest and is generally restricted to higher elevations – approximately 600 to 1200 meters above sea level. It occurs at very low densities in lowland forests. Within its optimal altitudinal range, it prefers to reside in basalt soil rainforest, with densities twice as high on basaltic soil as on acid igneous or metamorphic rock substrate (possibly due to basalt soil’s higher nutrient content). It may inhabit secondary and remnant forest patches as small as 20 hectares. Preferred habitats include microphyll vine forest, notophyll vine forest (both complex and simple), sclerophyll communities, and cleared land. Dendrolagus lumholtzi is often found in edge forest communities. It is unclear if this is where it spends the majority of its time, or if this is just where it is most easily spotted by humans. It is hypothesized that D. lumholtzi may prefer drier edge communities because too much rain leeches nutrients from the soil.

Range elevation: 600 to 1200 m.

Habitat Regions: tropical ; terrestrial

Terrestrial Biomes: rainforest

  • Kanowski, J., L. Felderhof, G. Newell, T. Parker, C. Schmidt, B. Stirn, R. Wilson, J. Winter. 2001. Community survey of the distribution of Lumholtz's Tree-kangaroo on the Atherton Tablelands, north-east Queensland. Pacific Conservation Biology, 7/2: 79-86.
  • Martin, R. 2005. Tree-Kangaroos of Australia and New Guinea. Collingwood: CSIRO Publishing.
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Habitat and Ecology

Habitat and Ecology
It is found in wet rainforests, and often in secondary forests. Occasionally found in dry and fringing eucalypt forests. They are known to forage in agricultural areas. This species is nocturnal, cryptic, and territorial. Its diet consists of fruit and leaves of a variety of rainforest plants (Maxwell et al. 1996).

Systems
  • Terrestrial
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Trophic Strategy

Lumholtz’s tree kangaroos are generalist herbivores, feeding on the leaves of at least 37 species of plants, including trees, vines, shrubs, and epiphytes. While they most often consume adult leaves, individuals have been observed eating young leaves or flowers. Examples of species eaten include Cryptocarya triplinervis of the Lauraceae family, Alstonia scholaris of the Apocynaceae family, and Ripogonum album of the Vitaceae family. Interestingly, Lumholtz’s tree kangaroos have been observed feeding on several species of plant that are toxic to most mammals – these include weedy Lantana camara, shining stinging trees (Dendrocnide photinophylla), and wild tobacco plants (Solanum mauritianum). Lumholtz’s tree kangaroos have never been observed drinking water and there are no bodies of water within the home ranges of most individuals. They are thought to obtain enough water from moisture in and on their food. When feeding, they move the forelimbs simultaneously to grab leaves, bring them closer to the mouth, and then chew. Digestion includes foregut fermentation. Although foliage is abundant in the canopy, Lumholtz’s tree kangaroos cannot feed on all types of leaves; it is therefore not known whether food is a limiting resource.

Plant Foods: leaves; flowers

Primary Diet: herbivore (Folivore )

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Associations

As generalist arboreal folivores, Lumholtz’s tree kangaroos fill a broad ecological niche. They occur sympatrically with other arboreal folivores, Trichosaurus vulpecula johnstoni and Pseudocheirus archeri. However, direct ecological competition is avoided by food partitioning - the diet of Lumholtz’s tree kangaroos consists of leaves higher in fiber and lower in nitrogen than the preferred foods of the other folivores. The role of this species’ scat as a soil fertilizer or a seed dsiperser has not been well studied.  As well as a prey species to dingoes, wild dogs, humans, and probably pythons, Lumholtz’s tree kangaroos are hosts to various parasites. They host microscopic pathogens, including the zoonotic bacterium Burkholderia pseudomallei, various species of Mycobacterium, and the coccidian Toxoplasma gondi. All of these endoparasites can be fatal. Lumholtz’s tree kangaroos are hosts to the heterodoxus louse, (Heterodoxus pygidialis), a harmless ectoparasite; and they have an endosymbiotic relationship with many species of nematode and a species of cestode (Progamotaenia dendrolagi), most of which live in the gut.

Mutualist Species:

Commensal/Parasitic Species:

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The main anti-predator adaptation of Lumholtz’s tree kangaroos is crypsis. Because they are small, solitary, nocturnal, and often high in the canopy, they are hard to find. Known predators are feral dogs (Canis lupus familiaris), dingoes (Canis lupus dingo), and humans (Homo sapiens). They are also probably eaten by amethystine pythons (Morelia amethistina), which are known predators of Bennett’s tree kangaroos. It is possible that juveniles are hunted by wedge-tailed eagles (Aquila audax).

Known Predators:

Anti-predator Adaptations: cryptic

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Life History and Behavior

Behavior

Adults do not generally communicate with each other. However, they are capable of vocalization when agitated or disturbed. Vocalizations include a soft ‘pffft’ exhalation noise when mildly agitated and a louder ‘woof’ and moaning when more agitated. All of these noises are relatively soft, none audible from over 30 m away by a human. Hearing is not thought to be particularly well developed in D. lumholtzi, as the pinnae are smaller than those of terrestrial macropods. The relative importance of sight and smell are not well studied. It is thought, however, that males use olfactory cues to determine when females are in estrous.

Communication Channels: tactile ; acoustic

Other Communication Modes: pheromones

Perception Channels: visual ; tactile ; acoustic ; chemical

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Life Expectancy

There is little information about the lifespan of D. lumholtzi, but D. matschiei, a closely related tree kangaroo, has been reported to live for up to 20 years in captivity.

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Reproduction

Dendrologous lumholtzi exhibits a promiscuous, non-seasonal mating system, in which a male and a female likely form a brief consort relationship. The consort will stay together for a maximum of several days, during which copulation may occur up to three times a day. It is thought that a male will patrol his home range, approaching females whose ranges overlap with his. He will use olfactory and behavioral cues to determine whether a female is in estrous. Before copulation, a male will repeatedly sniff the female’s cloaca and pouch, probably to detect pheromones indicative of estrous. The male will then position himself behind the female, rub his head, neck, and shoulders against the cloaca, and proceed to mate. Copulation may last from 10 to 35 minutes. In captivity, copulation occurs most frequently on the ground; however, it is unknown if this occurs in the wild. A copulatory plug inhibits later fertilization by the sperm of other males. Active mate guarding and competition have not been observed.

Mating System: polygynandrous (promiscuous)

Breeding is non-seasonal. The female estrous cycle is between 47 and 64 days, with an average of 56.4 days. The length of gestation is between 42 and 48 days, with an average of 44.8 days. The young uses the mother’s pouch for approximately a year after birth; a joey will begin to look outside the pouch at approximately 250 days, and will make its first foray from the pouch at approximately 300 days. The young will continue to suckle the mother for about a month or two after it has permanently left the pouch. A juvenile may remain in its mother’s home range up to 650 days after birth. A mother will usually come into estrous about two months after its young has permanently left the pouch; the average inter-birth interval is 1.4 years and 1 offspring is produced per birth. There is no evidence that females exhibit postpartum estrous or embryonic diapause. Females reach sexual maturity at approximately 2.04 years, whereas males reach sexual maturity at approximately 4.6 years.

Breeding interval: Average inter-birth interval is 1.4 years.

Breeding season: Mating occurs year-round.

Average number of offspring: 1.

Range gestation period: 42 to 48 days.

Average gestation period: 44.8 days.

Average weaning age: 13-14 months.

Average time to independence: 13-14 months.

Average age at sexual or reproductive maturity (female): 2.04 years.

Average age at sexual or reproductive maturity (male): 4.6 years.

Key Reproductive Features: iteroparous ; year-round breeding ; gonochoric/gonochoristic/dioecious (sexes separate); sexual ; viviparous

Aside from providing sperm for fertilization, adult males put forth no parental investment. An adult female, on the other hand, invests very much in her young. A mother allows her young to stay in the pouch for about 1 year and continues to suckle for 1 or 2 months afterwards. As the young begins to leave the pouch, the mother is protective, sometimes grabbing it and encouraging it to return. Mothers invest a large amount in teaching their offspring which leaves to eat and how to maneuver safely high in the canopy. Mother-young behavioral interactions involve frequent physical contact, often initiated by the young. The young disperses from the mother’s home range by 650 days after birth.

Parental Investment: altricial ; female parental care ; pre-fertilization (Provisioning, Protecting: Female); pre-hatching/birth (Provisioning: Female, Protecting: Female); pre-weaning/fledging (Provisioning: Female, Protecting: Female); pre-independence (Provisioning: Female, Protecting: Female); extended period of juvenile learning

  • Johnson, P., S. Delean. 2003. Reproduction of Lumholtz's tree-kangaroo, <<Dendrolagus lumholtzi>> (Marsupialia : Macropodidae) in captivity, with age estimation and development of the pouch young. Widlife Research, 30/5: 505-512.
  • Martin, R. 2005. Tree-Kangaroos of Australia and New Guinea. Collingwood: CSIRO Publishing.
  • Procter-Gray, E. 1985. The Behavior and Ecology of Lumholtz's Tree-Kangaroo, Dendrolagus lumholtzi (Marsupialia: Macropodidae). Cambridge: Harvard University.
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Molecular Biology and Genetics

Molecular Biology

Barcode data: Dendrolagus lumholtzi

The following is a representative barcode sequence, the centroid of all available sequences for this species.


No available public DNA sequences.

Download FASTA File
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Statistics of barcoding coverage: Dendrolagus lumholtzi

Barcode of Life Data Systems (BOLDS) Stats
Public Records: 1
Specimens with Barcodes: 1
Species With Barcodes: 1
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Conservation

Conservation Status

Lumholtz’s tree kangaroos are a species of least concern on the IUCN Red List and are not listed on the CITES appendices. However, relatively little of their range is protected, and habitat loss is the biggest potential threat to their well-being. Given their low birthrate and preference for small patches of isolated forest, they are quite vulnerable to habitat loss.

US Federal List: no special status

CITES: no special status

State of Michigan List: no special status

  • 2012. "Appendices I, II, and III. Convention on International Trade in Endangered Species of Wild Fauna and Flora" (On-line). CITES. Accessed April 13, 2012 at http://www.cites.org/eng/app/index.php.
  • Winter, J., S. Burnett, R. Martin. 2011. "Dendrolagus lumholtzi" (On-line). IUCN Red List of Threatened Species. Accessed April 13, 2012 at www.iucnredlist.org.
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IUCN Red List Assessment


Red List Category
LC
Least Concern

Red List Criteria

Version
3.1

Year Assessed
2008

Assessor/s
Winter, J., Burnett, S. & Martin, R.

Reviewer/s
Lamoreux, J. & Hilton-Taylor, C. (Global Mammal Assessment Team)

Contributor/s

Justification
Listed as Least Concern because, although its extent of occurrence is less than 20,000 km2 and there have been significant historical declines: it is common in suitable habitat, tolerant of some degree of habitat degradation, much of its range is contained within a protected area, there are presently no major threats, no evidence of a current decline in extent or quality of habitat, and the populations are generally thought to be secure.

History
  • 1996
    Lower Risk/near threatened
    (Baillie and Groombridge 1996)
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Population

Population
This species is common in suitable habitat.

Population Trend
Stable
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Threats

Major Threats
Historically, the main threat has been reduction of habitat, but this has ceased with the declaration of the Wet Tropics World Heritage Area, and the species appears to have been able to persist in the mosaic of fragmented habitat (particularly where there are available habitat corridors). On the Atherton Tableland, increased fragmentation makes them more vulnerable to predation by dogs, although strategic reforestation on the Atherton Tableland opens the possibility of some recovery of its original area of occupancy in the future (Maxwell et al. 1996). In agricultural areas where it occurs, predation by dogs and road kills represent threats.
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Management

Conservation Actions

Conservation Actions
This species is present in the Wet Tropics World Heritage Area. The species has been promoted as a flagship species, and it has a very high profile in the region where it occurs. Recommended conservation actions for this species from Maxwell et al. (1996), include: monitor distribution and abundance; study habitat utilisation and population dynamics in fragmented and regenerating rainforest habitats.
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Relevance to Humans and Ecosystems

Benefits

There are no known adverse effects of D. lumholtzi on humans.

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Lumholtz’s tree kangaroos have been hunted by indigenous Australian populations for thousands of years (Dendrolagus means “tree hare”), but the practice has essentially stopped. The species may be of slight economic importance as a source of ecotourism in Northeast Queensland.

Positive Impacts: ecotourism

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Wikipedia

Lumholtz's tree-kangaroo

Lithograph of Dendrolagus lumholtzi by Joseph Smit, from Proceedings of the general meetings for scientific business of the Zoological Society of London, 1884

Lumholtz's tree-kangaroo (Dendrolagus lumholtzi) is a heavy-bodied tree-kangaroo found in rain forests of the Atherton Tableland Region of Queensland. Its status is classified as least concern[2] by the IUCN, although local authorities classify it as rare.[3] It is named after the Norwegian explorer Carl Sofus Lumholtz (1851–1922).[4]

Description[edit]

It is the smallest of all tree-kangaroos, with males weighing an average of 7.2 kg (16 lbs) and females 5.9 kg (13 lbs).[5] Its head and body length ranges from 480–650 mm, and its tail, 600–740 mm.[6] It has powerful limbs and has short, grizzled grey fur. Its muzzle, toes and tip of tail are black.

Social behaviour[edit]

Lumholtz's tree-kangaroo lives in small, loose-knit groups of three to five, consisting of a male and female mates. Each kangaroo maintains a "home range" and will be hostile towards a member of the same gender that enters it (the one exception seems to be non-hostile encounters between adult males and their male offspring). Thus, the male will protect his own range, and visit the ranges of the females in his group. Mating takes place in episodes of about twenty minutes, and is often quite aggressive.

References[edit]

  1. ^ Groves, C. P. (2005). Wilson, D. E.; Reeder, D. M, eds. Mammal Species of the World (3rd ed.). Baltimore: Johns Hopkins University Press. p. 60. OCLC 62265494. ISBN 0-801-88221-4. 
  2. ^ a b Winter, J., Burnett, S. & Martin, R. (2008). Dendrolagus lumholtzi. In: IUCN 2008. IUCN Red List of Threatened Species. Retrieved 12 Oct 2008. Database entry includes justification for why this species is of Least Concern
  3. ^ "Lumholtz's tree-kangaroo". Queensland Government. 2005-08-30. Retrieved 2006-10-09. 
  4. ^ "Carl Sofus Lumholtz - biography". Biography. Australian National Herbarium. 17 December 2009. Retrieved 3 November 2010. "citing: J.W. Cribb, The Queensland Naturalist, Vol.44, Nos.1-3, 2006" 
  5. ^ Flannery, Timothy F, Martin, Roger, Szalay, Alexandria (1996). Tree Kangaroos: A Curious Natural History. Australia: Reed Books. ISBN 0-7301-0492-3. Retrieved 2006-11-25. 
  6. ^ Cronin, Leonard (2000). Australian Mammals: Key Guide (Revised Edition). Annandale, Sydney, Australia: Envirobooks. ISBN 0-85881-172-3. 
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