Macropodidae: Difference between revisions
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[[Image:Quokka cropped.jpg|thumb|[[Quokka]] with young]] |
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In addition, there is a linkage between the hopping action and breathing. As the feet leave the ground, air is expelled from the lungs by what amounts to an internal piston; bringing the feet forward ready for landing fills the lungs again, providing further energy efficiency. Studies of kangaroos and wallabies have demonstrated that, beyond the minimum energy expenditure required to hop at all, increased speed requires very little extra effort (much less than the same speed increase in, say, a horse, a dog, or a human), and also that little extra energy is required to carry extra weight — something that is of obvious importance to females carrying large pouch young |
In addition, there is a linkage between the hopping action and breathing. As the feet leave the ground, air is expelled from the lungs by what amounts to an internal piston; bringing the feet forward ready for landing fills the lungs again, providing further energy efficiency. Studies of kangaroos and wallabies have demonstrated that, beyond the minimum energy expenditure required to hop at all, increased speed requires very little extra effort (much less than the same speed increase in, say, a horse, a dog, or a human), and also that little extra energy is required to carry extra weight — something that is of obvious importance to females carrying large pouch young.<ref>Isolation of Succinivibrionaceae Implicated in Low Methane Emissions from Tammar Wallabies P. B. Pope, Science 333, 646 (2011)</ref> |
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The ability of larger macropods to survive on poor-quality, low-energy feed, and to travel long distances at high speed without great energy expenditure (to reach fresh food supplies or waterholes, and to escape predators) has been crucial to their evolutionary success on a continent that, because of soil fertility and low, unpredictable average rainfall, offers only very limited primary plant productivity. |
The ability of larger macropods to survive on poor-quality, low-energy feed, and to travel long distances at high speed without great energy expenditure (to reach fresh food supplies or waterholes, and to escape predators) has been crucial to their evolutionary success on a continent that, because of soil fertility and low, unpredictable average rainfall, offers only very limited primary plant productivity. |
Revision as of 13:37, 1 June 2012
Macropods[1] Temporal range: Oligocene to Recent Late | |
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Red-necked Wallaby | |
Scientific classification | |
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Family: | Macropodidae Gray, 1821 |
Genera | |
Macropods are marsupials belonging to the family Macropodidae, which includes kangaroos, wallabies, tree-kangaroos, pademelons, and several others. Macropods are native to Australia, New Guinea, and some nearby islands.[2] Before European settlement of Australia, there were about 53 species of Macropods. Six species have since become extinct. Another 11 species have been greatly reduced in numbers. Other species (e.g. Simosthenurus, Propleopus, Macropus titan) became extinct after the Australian Aborigines arrived and before the Europeans arrived.
Physical description
Although there were carnivorous kangaroos in the past, modern macropods are herbivorous: some are browsers, but most are grazers and are equipped with appropriately specialised teeth for cropping and grinding up fibrous plants, in particular grasses and sedges. In general, macropods have a broad, straight row of cutting teeth at the front of the mouth, no canine teeth, and a gap before the molars. The molars are large and, unusually, do not appear all at once but a pair at a time at the back of the mouth as the animal ages, eventually becoming worn down by the tough, abrasive grasses and falling out. Most species have four molars and, when the last pair is too worn to be of use, they starve to death[citation needed]. The dental formula for macropods is 3.0-1.2.41.0.2.4
Like the eutherian ruminants of the northern hemisphere (sheep, cattle, and so on), macropods have specialised digestive systems that use a high concentration of bacteria, protozoans, and fungi in the first chamber of a complex stomach to digest plant material. The details of organisation are quite different, but the end result is somewhat similar.
The particular structure-function relationship of macropodidae gut and their gut microbiota allows the degradation of lignocellulosic material with a relatively low emission of methane relative to other ruminants. The low emissions of methane are partly explained by the anatomically differences between the macropodid digestive system and that of other ruminants resulting in shorter retention times of particulate digesta within the foregut. This fact might prevent establishment of methanogenic archaea which has been found in low levels in tammar wallabies (Macropus eugenii) and eastern grey kangaroo (M. giganteus). Methagenomic analysis revealed that the foregut of tammar wallabies mainly contains bacteria belonging to the phyla Firmicutes, Bacteroides and Proteobacteria. Among proteobacteria populations of the Succinivibrionaceae family are overrepresented and may contribute to low methane emissions.[citation needed]
Macropods vary in size considerably but most have very large hind legs and a long, powerfully muscled tail. The term macropod comes from the Greek for "long foot" and is appropriate: most have a very long, narrow hind foot with a distinctive arrangement of toes: the fourth toe is very large and strong, the fifth toe moderately so, the second and third are fused and the first toe is usually missing. The short front legs have five separate digits. Some macropods have 7 carpal bones instead of the usual 8 in mammals [1]. All have relatively small heads and most have large ears, except for tree-kangaroos, which must move quickly between tight branches. The young are born very small and the pouch opens forward.
The unusual development of the hind legs is optimised for economical long distance travel at fairly high speed. The greatly elongated feet provide enormous leverage for the strong legs. But there is more to the famous kangaroo hop: kangaroos and wallabies have a unique ability to store elastic strain energy in their tendons. In consequence, most of the energy required for each hop is provided "free" by the spring action of the tendons (rather than by muscular effort). The main limitation on a macropod's ability to leap is not the strength of the muscles in the hindquarters. It is the ability of the joints and tendons to withstand the strain of hopping.
In addition, there is a linkage between the hopping action and breathing. As the feet leave the ground, air is expelled from the lungs by what amounts to an internal piston; bringing the feet forward ready for landing fills the lungs again, providing further energy efficiency. Studies of kangaroos and wallabies have demonstrated that, beyond the minimum energy expenditure required to hop at all, increased speed requires very little extra effort (much less than the same speed increase in, say, a horse, a dog, or a human), and also that little extra energy is required to carry extra weight — something that is of obvious importance to females carrying large pouch young.[3]
The ability of larger macropods to survive on poor-quality, low-energy feed, and to travel long distances at high speed without great energy expenditure (to reach fresh food supplies or waterholes, and to escape predators) has been crucial to their evolutionary success on a continent that, because of soil fertility and low, unpredictable average rainfall, offers only very limited primary plant productivity.
Gestation in macropods lasts about a month, being slightly longer in the largest species. Typically, only a single young is born, weighing less than 1 gram (0.035 oz) at birth. They soon attach themselves to one of four teats inside the mother's pouch. The young leave the pouch after 5–11 months, and are weaned after a further 2–6 months. Macropods reach sexual maturity at 1–3 years of age, depending on species.[4]
Fossil record
The earliest known fossil macropod dates back about 11.61mya to 28.4mya, either in the Miocene or Late Oligocene, and was uncovered in South Australia. Unfortunately, the fossil could not be identified any further than the family. A Queensland fossil of a species similar to Hadronomas has been dated at around 5.33mya to 11.61mya, falling in the Late Miocene or Early Pliocene. The earliest completely identifiable fossils are from around 5.33mya.[5]
Classification
There are two living subfamilies in the Macropodidae family: Lagostrophinae is represented by a single species, the Banded Hare-wallaby; the remainder, about 60 species, makes up the subfamily Macropodinae.
- FAMILY MACROPODIDAE[1][6]
- Genus †Watutia
- Genus †Dorcopsoides
- Genus †Kurrabi
- Subfamily †Potoroinae
- Tribe †Potoroini
- Genus †Propleopus Longman, 1924
- Tribe †Potoroini
- Subfamily Lagostrophinae[7]
- Genus Lagostrophus
- Banded Hare-wallaby, Lagostrophus fasciatus
- Genus †Tropsodon
- Genus Lagostrophus
- Subfamily Sthenurinae
- Genus †Sthenurus
- Genus †Procoptodon
- Genus †Hadronomas
- Genus †Eosthenurus
- Subfamily †Balbarinae
- Genus †Nambaroo
- Genus †Wururoo
- Genus †Ganawamaya
- Genus †Balbaroo
- Genus †Silvaroo
- Subfamily Macropodinae
- Genus †Prionotemnus
- Genus †Congruus
- Genus †Baringa
- Genus †Bohra
- Genus †Synaptodon
- Genus †Fissuridon
- Genus †Protemnodon
- Genus Dendrolagus: tree-kangaroos
- Grizzled Tree-kangaroo, Dendrolagus inustus
- Lumholtz's Tree-kangaroo, Dendrolagus lumholtzi
- Bennett's Tree-kangaroo, Dendrolagus bennettianus
- Ursine Tree-kangaroo, Dendrolagus ursinus
- Matschie's Tree-kangaroo, Dendrolagus matschiei
- Doria's Tree-kangaroo, Dendrolagus dorianus
- Goodfellow’s Tree-kangaroo, Dendrolagus goodfellowi
- Lowlands Tree-kangaroo, Dendrolagus spadix
- Golden-mantled Tree-kangaroo, Dendrolagus pulcherrimus
- Seri's Tree-kangaroo, Dendrolagus stellarum
- Dingiso, Dendrolagus mbaiso
- Tenkile, Dendrolagus scottae
- Genus Dorcopsis
- Brown Dorcopsis, Dorcopsis muelleri
- White-striped Dorcopsis, Dorcopsis hageni
- Black Dorcopsis, Dorcopsis atrata
- Gray Dorcopsis, Dorcopsis luctuosa
- Genus Dorcopsulus
- Small Dorcopsis, Dorcopsulus vanheurni
- Macleay's Dorcopsis, Dorcopsulus macleayi
- Genus Lagorchestes
- †Lake Mackay Hare-wallaby, †Lagorchestes asomatus
- Spectacled Hare-wallaby, Lagorchestes conspicillatus
- Rufous Hare-wallaby, Lagorchestes hirsutus
- †Eastern Hare-wallaby, †Lagorchestes leporides
- Genus Macropus
- Subgenus Notamacropus
- Agile Wallaby, Macropus agilis
- Black-striped Wallaby, Macropus dorsalis
- Tammar Wallaby, Macropus eugenii
- †Toolache Wallaby, †Macropus greyii
- Western Brush Wallaby, Macropus irma
- Parma Wallaby, Macropus parma (rediscovered, thought extinct for 100 years)
- Pretty-faced Wallaby, Macropus parryi
- Red-necked Wallaby, Macropus rufogriseus
- Subgenus Osphranter
- Antilopine Kangaroo, Macropus antilopinus
- Black Wallaroo, Macropus bernadus
- Common Wallaroo, Macropus robustus
- Red Kangaroo, Macropus rufus
- Subgenus Macropus
- Western Grey Kangaroo, Macropus fuliginosus
- Eastern Grey Kangaroo, Macropus giganteus
- Subgenus Notamacropus
- Genus Onychogalea
- Bridled Nail-tail Wallaby, Onychogalea fraenata
- †Crescent Nail-tail Wallaby, †Onychogalea lunata
- Northern Nail-tail Wallaby, Onychogalea unguifera
- Genus Petrogale
- P. brachyotis species-group
- Short-eared Rock-wallaby, Petrogale brachyotis
- Monjon, Petrogale burbidgei
- Nabarlek, Petrogale concinna
- P. xanthopus species-group
- Proserpine Rock-wallaby, Petrogale persephone
- Rothschild's Rock-wallaby, Petrogale rothschildi
- Yellow-footed Rock-wallaby, Petrogale xanthopus
- P. lateralis/penicillata species-group
- Allied Rock-wallaby, Petrogale assimilis
- Cape York Rock-wallaby, Petrogale coenensis
- Godman's Rock-wallaby, Petrogale godmani
- Herbert's Rock-wallaby, Petrogale herberti
- Unadorned Rock-wallaby, Petrogale inornata
- Black-flanked Rock-wallaby, Petrogale lateralis
- Mareeba Rock-wallaby, Petrogale mareeba
- Brush-tailed Rock-wallaby, Petrogale penicillata
- Purple-necked Rock-wallaby, Petrogale purpureicollis
- Mt. Claro Rock-wallaby, Petrogale sharmani
- P. brachyotis species-group
- Genus Setonix
- Quokka: Setonix brachyurus
- Genus Thylogale
- Tasmanian Pademelon, Thylogale billardierii
- Brown's Pademelon, Thylogale browni
- Dusky Pademelon, Thylogale brunii
- Calaby's Pademelon, Thylogale calabyi
- Mountain Pademelon, Thylogale lanatus
- Red-legged Pademelon, Thylogale stigmatica
- Red-necked Pademelon, Thylogale thetis
- Genus Wallabia
- Swamp Wallaby or Black Wallaby, Wallabia bicolor
See also
References
- ^ a b Groves, C. P. (2005). Wilson, D. E.; Reeder, D. M. (eds.). Mammal Species of the World: A Taxonomic and Geographic Reference (3rd ed.). Baltimore: Johns Hopkins University Press. pp. 58–70. ISBN 0-801-88221-4. OCLC 62265494.
- ^ Clode, D (2006). Continent of curiosities: a journey through Australian natural history. Melbourne: Cambridge University Press. pp. 25–8. ISBN 978-0-521-86620-0.
- ^ Isolation of Succinivibrionaceae Implicated in Low Methane Emissions from Tammar Wallabies P. B. Pope, Science 333, 646 (2011)
- ^ Poole, WE (1984). Macdonald, D (ed.). The Encyclopedia of Mammals. New York: Facts on File. pp. 862–71. ISBN 0-87196-871-1.
- ^ The Paleobiology Database (2011). "Macropodidae (kangaroo)". The Paleobiology Database. Majura Park, ACT, Australia: Australian Research Council. Retrieved 11 July 2011.
- ^ Haaramo, M (20 December 2004). "Macropodidae: kenguroos". Mikko's Phylogeny Archive. Retrieved 15 March 2007.
- ^ Prideaux, GJ; Warburton, NM (2010). "An osteology-based appraisal of the phylogeny and evolution of kangaroos and wallabies (Macropodidae: Marsupialia)". Zoological Journal of the Linnean Society. 159 (4): 954–87. doi:10.1111/j.1096-3642.2009.00607.x.
External links