Procoptodon: Difference between revisions
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=== Habitat === |
=== Habitat === |
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''Procoptodon goliah'' was mainly known for living in semiarid areas of [[South Australia]] and [[New South Wales]]. These environments were harsh, characterized by vast areas of treeless, wind-blown sand dunes. However, around [[Lake Menindee]], in western New South Wales, had a cooler, wetter climate at the time ''Procoptodon'' existed. The surrounding area was a mosaic of sclerophyll forest, woodland, savannah and plains, but sand dunes would have also formed along the edges of the Menindee.<ref name=AustrlianMuseum/ |
''Procoptodon goliah'' was mainly known for living in semiarid areas of [[South Australia]] and [[New South Wales]]. These environments were harsh, characterized by vast areas of treeless, wind-blown sand dunes. However, around [[Lake Menindee]], in western New South Wales, had a cooler, wetter climate at the time ''Procoptodon'' existed. The surrounding area was a mosaic of sclerophyll forest, woodland, savannah and plains, but sand dunes would have also formed along the edges of the Menindee.<ref name=AustrlianMuseum/> |
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=== Physiology === |
=== Physiology === |
Revision as of 22:09, 6 May 2016
Procoptodon Temporal range:
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Procoptodon goliah | |
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Genus: | †Procoptodon Owen, 1873
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Procoptodon[1] was a genus of giant short-faced kangaroo living in Australia during the Pleistocene epoch. P. goliah, the largest known kangaroo that ever existed, stood approximately 2 m (6.6 ft).[2] They weighed about 232 kg (511 lb).[3] Other members of the genus are smaller, however, and Procoptodon gilli is the smallest of all of the sthenurine kangaroos, standing ~1m tall.
Procoptodon goliah
Habitat
Procoptodon goliah was mainly known for living in semiarid areas of South Australia and New South Wales. These environments were harsh, characterized by vast areas of treeless, wind-blown sand dunes. However, around Lake Menindee, in western New South Wales, had a cooler, wetter climate at the time Procoptodon existed. The surrounding area was a mosaic of sclerophyll forest, woodland, savannah and plains, but sand dunes would have also formed along the edges of the Menindee.[2]
Physiology
Appearance
Procoptodon physiology was likely similar to that of the contemporary kangaroo, however Procoptodon goliah were characterized by their large size. These sthenurines, or short-faced kangaroos, included species that were more than three times the size of the largest kangaroos today. The largest, Procoptodon goliah, was 2.7m tall and weighed up to 240 kg.[4] These animals lived alongside modern species of kangaroo, but specialised on a diet of leaves from trees and shrubs. P. goliah were giant, short-faced kangaroos that were distinguishable by their flat faces and forward-pointing eyes. On each foot they had a single large toe or claw somewhat similar in appearance to a horse's hoof. On these unusual feet they moved quickly through the open forests and plains, where they sought grass and leaves to eat. Their front paws were equally strange: each front paw had two extra-long fingers with large claws. It is possible that they were used to grab branches, bringing leaves within eating distance.[5]
Mobility
Procoptodon goliah were unable to hop as a mode of transportation, and would have been un-able to accelerate sufficiently due to their mass.[6] Broad hips and ankle joints adapted to resist torsion or twisting, point to an upright posture where weight is supported by one leg at a time, Their broad hips also allowed for another important modification: large buttocks - a feature shared with other walking species.[4] However, there is some ambiguity surrounding the possible locomotion of the P. goliah. Some research suggests that this species was perhaps the largest hopping mammal to have ever existed.[3] Research suggests that the most optimal weight for a large hopping marsupial is approximately 50–60 kg. Larger animals, especially the massive P. goliah, would be substantially more at risk of tendon breakage while hopping[3] If P. goliah were to have travelled by hopping, the highest possible balance between size and speed would have been peaked because their bodies would surely have been the largest possible to be carried by this method of locomotion [7] A more likely suggestion, based on the apparent anatomy allowed by the bone structure of P. goliah, is that unlike modern kangaroos, which are plantigrade hoppers at high speeds and use their tails in pentapedal locomotion at slower speeds, Procoptodon was an unguligrade biped, walking in a fashion similar to hominids.[6] Locomotion mechanics and physiology have been investigated through the examination of muscleoskeleton scaling patterns. The largest, Procoptodon goliah, was 2.7m tall and weighed up to 240 kg.[4] For Procoptodon goliah, tendon stress was identified, which indicates limited locomotor capabilities, exposing a correlation between body mass and locomotion abilities.[8] Ruptures in tendons demonstrate strain in elasticity of muscles in the limbs which provides evidence that perhaps the hypothesized ability for the Procoptodon goliah to hop may have been unlikely.[8] Due to their locomotive performance, the species may have been vulnerable to human predation.[8] Fossils of giant short-faced kangaroos have been found at the Naracoorte World Heritage fossil deposits in South Australia, Lake Menindee in New South Wales, Darling Downs in Queensland, and at many other sites. A full-size, lifelike replica is on permanent display with other ancient native Australian animals at the Australian Museum.[2]
The genus is paraphyletic, derived from Simosthenurus.[9]
Diet and Molar Patterns
These animals lived alongside modern species of kangaroo, but specialised on a diet of leaves from trees and shrubs.[4] Their robust skull architecture and shortened face has been thought to be related to increased masseter muscles used to chew foods. Dental microwear of P. goliah supports a browsing diet. Large bicuspids, crenulated dental crowns, and a massive bony jaw present in the fossil evidence of P. goliah would have been required to process and digest a substantial amount of leafy fodder [7] Stable isotopic data suggested its diet consisted of plants utilising a C4 photosynthetic pathway, typically associated with grasses. In this case, however, chenopod saltbushes found throughout semi-arid Australia were considered a more likely source of the C4 signature. [An intensification in aridity during the second half of the Pleistocene propagated the evolutionary progression of the P. goliah to adapt to an abundance of dry vegetation. Evidence that P. goliah was the most widely distributed species among the Pleistocene macropodids throughout the continent shows that this species was adapted to a tougher diet than any other extinct Pleistocene sthenurine (Systematics and Evolution of the Sthenurine Kangaroos). Similar to Macropus giganteus, Procoptodon has molar patterns that indicate they had a similar, grassy, herbivorous diet. What exactly Procoptodon ate is unknown, as its preference to either natural or artificial tasting foods cannot be learned from an extinct genus. [1] Through the study of isotopic composition of Procoptodon goliah tooth enamel, in addition to biomechanical bone features, dietary clues and feeding behavior have been deduced [10] The osteological features provide evidence of Procoptdon goliah's ability to handle fibrous vegetables and salt consumption. This in turn leads to the belief that the species needed to be close to a water source to deal with salt intake, however, at the same time some theories are beginning to arise that limb-remains indicate the ability to travel distances to and from water sources [10]
Possible Factors for Extinction
Human Interaction
The genus was present until at least about 50,000 years ago before going extinct, although there is some evidence they may have survived to as recently as 18,000 years ago. Its extinction may have been due to climate shifts during the Pleistocene,[2] or to human hunting.[5] Those who support the hypothesis of a human-mediated extinction process cite the fact that the arrival of humans to continental Australia occurred at approximately the same time as the disappearance of this species.[11] More evidence that this extinction was facilitated by human interaction is present in the fact that the time period in which the extinction occurred was characterized by a relatively stable climate.[11] However, there is no evidence of predation on or consumption of P. goliah by humans in the fossil record.[11]
Fossils of giant short-faced kangaroos have been found at the Naracoorte World Heritage fossil deposits in South Australia, Lake Menindee in New South Wales, Darling Downs in Queensland, and at many other sites. A full-size, lifelike replica is on permanent display with other ancient native Australian animals at the Australian Museum.[11]
Some researchers have speculated that the replacement of nutritious, fire-sensitive plants with less flammable, less nutritious flora brought about by human, fire-based deforestation in Australia played a large role in P. goliah and other Australian mega-fauna extinctions about 50kya. However, the diet of P. goliah , primarily chenopods and Atriplex in particular, were less flammable and remained largely unaffected by fire. These diet patterns disprove theories that the P. goliah’s extinction was due in large part to a reduction in food supply from fire.[5] At the same time, it is important to note that because of the kangaroos elongated breeding cycles, their ability to increase population numbers after human predation was highly limited [10]
Environmental Factors
Kangaroos living in dry, arid environments have been shown to exhibit higher densities of tooth enamel, caused by indirect hydration through consuming herb-enriched plants. Lower levels of this enamel in P. goliah teeth found in areas with similar environmental parameters compared to the modern grazing kangaroo suggests that it relied far more heavily on free standing water sources such as lakes and streams.[5]
Given the larger size of P. goliah and its tendency to favor larger, freestanding water sources, episodic droughts accumulating 55kya in the southern interior region of Australia would have certainly affected Goliath populations. Yet records show that such droughts had characterized this region for the previous 7 million years, with P. goliah surviving multiple intensely dry episodes during this period. Any period of significant decreases in rainfall did not occur until 5,000-10,000 years after the appromimate extinction of the P. goliah 45-50kya, 20ky before the last glacial maximum of high aridity. These factors disprove speculations that such droughts could have played a significant role in the extinction of P. goliah.[5]
Dental microwear of P. goliah supports a browse diet; however, stable isotopic data suggested its diet consisted of plants utilising a C4 photosynthetic pathway, typically associated with grasses. In this case, however, chenopod saltbushes found throughout semi-arid Australia were considered a more likely source of the C4 signature. Due to the saltbushes being their main food source, Procoptodon goliah was heavily dependent on free-standing water to help promote the processing of its salt-laten diet.[5][12]
There is evidence that supports both of the claims that the extinction of P. goliah may have been due to climate shifts during the Pleistocene[2] or to human hunting.[5] P. goliah, depending heavily on free-standing water, was more vulnerable to drought. This can explain why the red kangaroo survived the increasing aridity and Procoptodon goliah did not. However, there is also evidence that suggests that humans could have a significant influence in the extinction of P. goliah. Due to the fact of P. goliah needing a constant free-standing source of water, plus its height and its common habitat in open shrub lands made the P. goliah more noticeable to the human hunters, thus making it vulnerable to humans who were also water bound like the Procoptodon.[12]
References
- ^ Haaramo, M. (2004-12-20). "Mikko's Phylogeny Archive: Macropodidae - kenguroos". Retrieved 2007-03-15.
- ^ a b c d e "Procoptodon goliah". Australian Museum. Retrieved 2012-03-22.
- ^ a b c Helgen, K.M., Wells, R.T., Kear, B.P., Gerdtz, W.R., and Flannery, T.F. (2006). "Ecological and evolutionary significance of sizes of giant extinct kangaroos". Australian Journal of Zoology. 54 (4): 293–303. doi:10.1071/ZO05077.
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: CS1 maint: multiple names: authors list (link) - ^ a b c d Australian Geographic (2014). "Giant prehistoric kangaroos walked, not hopped".
{{cite journal}}
: Cite journal requires|journal=
(help) - ^ a b c d e f g Prideaux, G. J.; Ayliffe, L. K.; Desantis, L. R. G.; Schubert, B. W.; Murray, P. F.; Gagan, M. K.; Cerling, T. E. (2009-07-14). "Extinction implications of a chenopod browse diet for a giant Pleistocene kangaroo". Proceedings of the National Academy of Sciences. 106 (28): 11646–11650. doi:10.1073/pnas.0900956106.
- ^ a b Janis, CM; Buttrill, K; Figueirido, B (2014). "Locomotion in Extinct Giant Kangaroos: Were Sthenurines Hop-Less Monsters?". PLoS ONE. 9 (10): e109888. doi:10.1371/journal.pone.0109888. Retrieved October 15, 2014.
{{cite journal}}
: CS1 maint: unflagged free DOI (link) - ^ a b Webb, Steve. Corridors to Extinction and the Australian Megafauna. Burlington: Elsevier Science, 2013. Print.
- ^ a b c McGowan, C.P.; Skinner, J.; Biewener, A.A. (Feb 2008). "Kangaroos and human Aborigines". Journal of Anatomy. 212: 153–163. doi:10.1111/j.1469-7580.2007.00841.x. PMC 2408984. PMID 18086129.
- ^ Prideaux G (2004). "Systematics and Evolution of the Sthenurine Kangaroos". University of California Publications in Geological Sciences. 146: 1–642. doi:10.1525/california/9780520098459.001.0001. Retrieved 2012-03-22.
- ^ a b c Dawson, Terrence (2012). Kangaroos (2 ed.). Collingwood, Vic.: CRISO. pp. 169–170. Retrieved 20 October 2014.
- ^ a b c d Cite error: The named reference
Wroe2013
was invoked but never defined (see the help page). - ^ a b Field, Judith and Wroe, Stephen. Aridity, faunal adaptations and Australian Late Pleistocene extinctions. World Archaeology. Mar 2012, Vol. 44 Issue 1, p56-74. 19p.