Ctenophorus decresii - Misplaced Pages

Species of lizard

Ctenophorus decresii

Photograph of a tawny dragon
Conservation status
Least Concern (IUCN 3.1)
Scientific classification
Domain:	Eukaryota
Kingdom:	Animalia
Phylum:	Chordata
Class:	Reptilia
Order:	Squamata
Suborder:	Iguania
Family:	Agamidae
Genus:	Ctenophorus
Species:	C. decresii
Binomial name
*Ctenophorus decresii* (A.M.C. Duméril & Bibron, 1837)
Synonyms
Grammatophora decresii A.M.C. Duméril & Bibron, 1837 Agama decresiensis Fitzinger, 1843 Ctenophorus decresii — Fitzinger, 1843 Amphibolurus decresii — Boulenger, 1885 Ctenophorus decresii — Manthey & Schuster, 1999

Ctenophorus decresii, also known commonly as the tawny dragon, tawny crevice-dragon, or tawny rock dragon, is a species of lizard in the family Agamidae. The species is endemic to Australia.

C. decresii is known for its variations in throat colours which change based on environmental conditions. Its primary food sources consist of both vegetation and invertebrates, and it prefers to live in rocky habitats. The average snout-to-vent length (SVL) of the species is 80.76 mm (3.180 in), with larger individuals being around 89 mm (3.5 in) and smaller individuals around 72 mm (2.8 in). The optimal time for mating in this species is two to three weeks after the females emerge from hibernation. Eggs are typically laid from September to October with most of them being laid earlier in the period.

Etymology and taxonomy

C. decresii is a member of the genus Ctenophorus, which is a very diverse group of lizards found throughout Australia. The specific name, decresii, refers to L'Île de Decrès, which was the French name for Kangaroo Island in 1837. The usual common names for the species are tawny dragon, tawny crevice-dragon, and tawny rock dragon.

The entire genus of lizards is sexually dimorphic, in which males and females exhibit different characteristics. Neck and overall colouration distinguishes male lizards from female and juvenile lizards.

Description

C. decresii are often characterised by the colour of their throats. Variations of colour in these lizards were previously attributed to different levels in sexual maturity. However, these variations are most likely due to environmental conditions such as "maternal effects, incubation conditions or post-hatching conditions". There is also a possibility that genetics are primarily responsible for the variations. The colours of male lizards can vary, but they are usually orange only, yellow only, orange surrounded by yellow, or grey only throats. The colours can also vary in degree of intensity and are due to different lineages, northern and southern. Males with orange throats tend to be more aggressive when it comes to defending their territory. It is still unclear how the lineages of females impact the expression of their colours especially since females from wither lineage tend to have the same colouration. From this, it can be concluded that throat colour in these lizards is polymorphic, specifically in determining whether the phenotype is yellow or orange. Although both colours are polymorphic, the yellow colour is also greatly influenced by environment and levels of testosterone present. Polymorphism and environmental factors play major roles in colour expression, but it is impossible to say which one is more significant without genomic analysis and linkage mapping.

The average snout-to-vent length (SVL) of the species is 80.76 mm (3.180 in) with larger individuals being around 89 mm (3.5 in) and smaller individuals around 72 mm (2.8 in).

Magnetic resonance imaging (MRI) has been used on the tawny dragon lizards to examine their brains. A study found that the brain had 224 structures that could be seen. The left hemisphere in the brain is associated with the optic system. This research was fundamental in the study of evolutionary neuroscience in lizards. By having the neuroanatomy of lizards, scientists are able to see how behaviour and cognitive function are related to structures of the brain.

Polymorphism

Ctenophorus decresii is known to display polymorphisms in throat colouration. Within the species C. decresii, morphs can range from grey and white to a bright red. Some of the variants include multi-coloured, grey, yellow, orange, blue, and red-throated lizards. This variation comes from the diverse geographic locations in which C. decresii can be found, such as South Australia, New South Wales, and other areas throughout Australia. One geographic location may favor a certain throat colour for C. decresii, while a different location may favor a different colour.

Although there is a lot of diversity in throat colours, the colour variants in the throats are discrete, meaning the morphologies of individual lizards could be placed into specific categories After using objective methods to identify the colour morphs, statistical tests were run. The tests analyzed variation based on granularity, segmentation, and comparison with visual background. One group of lizards had similar granularity, segmentation, and colouration. Another group also had similar granularity, segmentation, and colouration that differed from the first group. There were very few lizards with in-between phenotypes. However, within the categories, there still is slight variation in the shades of colours of the lizards. Because throat colouration is a discrete trait, it is highly heritable. This is a key reason that the discrete colour variation has been maintained over multiple generations. The offspring will have similar or the same colouration as the parents, therefore making the colouration carry out over generations.

C. decresii's diversity in discrete throat colour may be caused by a combination of sexual selection and natural selection.

The C. decresii throat colours can be classified into two main, discrete categories—dull and bright-coloured. The dull-coloured throats give lizards a fitness advantage because the lizards are harder for predators, like birds, to see. The dull throats allow the lizards to avoid predators and survive longer; therefore, this trait became more prevalent in that population of lizards.

However, bright-coloured throats also give the lizards a fitness advantage because the bright-coloured throats attract more females, and therefore those males are more likely to reproduce. Although the bright-coloured throats increase the likelihood of being eaten by predators, they also increase sexual success. Therefore, the prevalence of bright-coloured throats is maintained in this population of lizards. Based on the conflicting benefits of dull and bright-coloured throats, it is understandable that both morphs have been maintained in this species. Each trait gives a lizard a different evolutionary advantage.

Diet

C. decresii consume a wide variety of foods and are omnivores. Their main diet consists of invertebrates and vegetation. Invertebrates include crickets, moths, fly maggots, and locusts.

Habitat and geographic range

C. decresii is endemic to Australia. While the species is most commonly found in rocky areas throughout Australia, its exact habitat varies as it is found in a few distinct locations throughout Australia.

Scientists have identified the different populations of lizards as separate lineages due to geographic isolation. The three lineages of C. decresii are the northern, southern, and New South Wales lineages. In New South Wales, they are found in the far west of the state, in the Barrier Ranges, near Silverton, among other locations. The entire genus Ctenophorus maintains a generally constant body shape, adapted for the Australian climate.

Behaviour

Reproduction

C. decresii are characterized by their ability to produce multiple clutches in a year but a short lifespan. Eggs are typically laid from September to October, with most of them being laid earlier in the period.

Incubation temperature affects the hatchling tail length and sex. At intermediate incubation temperatures, the proportion of males to females was much higher compared to extreme incubation temperatures (very high or very low) where females were the only sex seen. This shows that the season in which the females lay the eggs is good indicator of which sex will be seen in the hatchlings and body size, also known as temperature-dependent sex determination. Very low incubation temperatures are often associated with slower, less developed hatchlings. If incubated at a suitable temperature, hatchlings will have a higher body mass. These individuals will also have a higher probability of reproductive success especially in terms of clutch size and offspring body mass. Studies suggest that body mass is also influenced by the length of incubation. Eggs laid closer to the beginning of the season have more time to develop thus giving them more of an opportunity to gain more body mass. On the other hand, those laid later in the season do not have the same opportunity. Larger body sizes provide an advantage to males and females. Males are better able to defend their territories, and females have higher fecundity. Males with more territory also had larger body masses.

Mating

As mentioned in the description section, the colouration of the male tawny dragon lizards can vary, especially by region (northern and southern). For mating, southern females are more likely to mate with southern males however, they are much less selective in their mate preferences than northern females. Both southern and northern males are more likely to be rejected by northern females. Southern males also prefer to mate with southern females because they share the same lineage. This suggests that preferences by either sex are driven by behavioural differences regionally. These lizards primarily prefer to mate with partners that are in the same region geographically. Overall, it appears that speciation is primarily driven by sexual selection with neither sex being more selective than the other.

Male-male interactions

In these lizards, northern males are considered more aggressive than southern males. Orange, northern males are the most aggressive, and southern males are the least aggressive. But, regardless of lineage, males can differentiate their aggression. Aggression occurs at a higher rate when two males have not interacted with one another. When encountering a male that he had encountered before aggression was significantly lower. Repeated interactions were shown to more effective in limiting aggression between males. If there has already been a previous encounter, it is less likely that the individual will be a threat to the livelihood or territory of that male. Being able to recognize which lizards they have already encountered gives lizards the opportunity to limit costly interactions. They are able to tell which individuals they have already won or lost to. To distinguish between individuals, the lizards use physical characteristics as opposed to chemical or behavioural cues. This species uses colouration of the throats to distinguish between lizards, similar to how scientist do in experiments. When researchers controlled for throat colouration, it was more difficult for lizards to determine if they had already encountered the lizard. There were similar levels of aggression for familiar and unfamiliar males.

Another indicator of aggression is the presence of black chest patches. Males with these patches are not only more aggressive but also more likely to initiate and win fights. Size and residency status also seem to be deciding factors in the winner of territories with size being a bit more important. Regardless of size, residents are more effective at defending their territories against non-residents. In these cases, larger males do not have the advantage. However, when both lizards are residents (or non-residents), the larger lizard has more success at defending their territory.

A higher level of aggression is also associated greater number of encounters with other lizards, specifically those where they are the initiator of the fight. If a male is initiating more fights, it can be assumed that they are the more dominant individual. This also means these males reside in territories that are rich with resources that must be defended in order for them to maintain their dominance. High aggression is associated with a greater degree of territorialism.

Conservation

Habitat loss

The effects of climate change, specifically rising temperatures, have caused significant declines in many species, and the tawny dragon lizard is not an exception. In high temperatures, the tawny dragon lizard has adapted effectively regulate their body temperature through a process called behavioural thermoregulation, but there is a cost. Because of this, water loss occurs at a much higher rate leading to desiccation, or drying, more quickly. The combination of high temperatures and decreased rainfall has had a severe impact on the not only survival of these lizards but also fecundity and growth rate. As these conditions continue to become more extreme, these problems will become increasingly more severe.

C. decresii are also threatened by habitat fragmentation and bush rock removal. These lizards already have specific habitat requirements, so any habitat loss can increase the risk of decline. The population size is trending downwards, because their habitat range is becoming so small in some areas. Although many of these problems are driven by humans, grazing animals impact the population as well. Constant grazing from animals like sheep, cattle, and feral goats reduce the areas where the lizards can hide and live. With fewer hiding places, they are more susceptible to predation. This, in conjunction with human land clearing, causes much less genetic variation within the species.

Protective colourism and behaviour

Cryptic behaviour

The intensity of colours in these lizards indicates the amount predation they are susceptible to. As expected, individuals with more brightly coloured bodies are at a higher risk of predation, because they are more easily spotted. In these habitats, the rocks in which the lizards bask are darker, so the bright oranges and yellows contrast greatly Individuals that are not as bright, or duller, are attacked significantly less than their brightly coloured counterparts. The main predator of the tawny dragon lizard is birds. C. decresii are a species that use crypsis as a defense mechanism, however females use this mechanism more than males. Although more prevalent in females, both sexes use the colouration to blend it with their surroundings. The exact colours depend on the environment, but the colourations are usually localized to the exposed body regions, so individuals can avoid predation.

Depending on the environmental conditions, C. decresii can be more or less conspicuous. Typically, the most abundant rock colours are grey or orange. The colours differ in the region where the lizards reside. Dorsal and lateral colouration are vital in ensuring individuals in either region are not as susceptible to predators. The lizards are least conspicuous when their colour matches the abundant rock colour of their region. When individuals are placed in the opposite region, they are at a much more conspicuous/noticeable. However, individuals can still use behavioural tactics to protect themselves from predators even though they stand out more.

References

^ Melville, J.; Hutchinson, M.; Clemann, N.; Robertson, P. (2018). "Ctenophorus decresii ". IUCN Red List of Threatened Species. 2018: e.T83410125A83453693. doi:10.2305/IUCN.UK.2018-1.RLTS.T83410125A83453693.en. Retrieved 20 November 2021.
^ Ctenophorus decresii at the Reptarium.cz Reptile Database. Accessed 11 February 2021.
Beolens, Bo; Watkins, Michael; Grayson, Michael (2011). The Eponym Dictionary of Reptiles. Baltimore: Johns Hopkins University Press. xiii + 296 pp. ISBN 978-1-4214-0135-5. (Ctenophorus decresii, p. 67).
^ New South Wales Archaeology Pty Ltd (October 2008). "3. Tawny Rock Dragon Report: Status and distribution of the Tawny Rock Dragon and their habitat" (PDF). Proposed development of Stage 1b and 1c, Silverton Wind Farm, far western New South Wales. Retrieved 23 December 2024.
Teasdale, L. C.; Stevens, M.; Stuart-Fox, D. (2013). "Discrete colour polymorphism in the tawny dragon lizard (Ctenophorus decresii) and differences in signal conspicuousness among morphs". Journal of Evolutionary Biology. 26 (5): 1035–1046. doi:10.1111/jeb.12115. ISSN 1420-9101. PMID 23495663. S2CID 33168207.
^ McLean, Claire A.; Bartle, Richard A.; Dong, Caroline M.; Rankin, Katrina J.; Stuart-Fox, Devi (1 October 2020). "Divergent male and female mate preferences do not explain incipient speciation between lizard lineages". Current Zoology. 66 (5): 485–492. doi:10.1093/cz/zoaa010. ISSN 2396-9814. PMC 7705505. PMID 33293929.
Rankin, Katrina J.; McLean, Claire A.; Kemp, Darrell J.; Stuart-Fox, Devi (6 September 2016). "The genetic basis of discrete and quantitative colour variation in the polymorphic lizard, Ctenophorus decresii ". BMC Evolutionary Biology. 16 (1): 179. doi:10.1186/s12862-016-0757-2. ISSN 1471-2148. PMC 5012029. PMID 27600682.
Umbers, Kate D. L.; Osborne, Louise; Keogh, J. Scott (15 October 2012). "The Effects of Residency and Body Size on Contest Initiation and Outcome in the Territorial Dragon, Ctenophorus decresii ". PLOS ONE. 7 (10): e47143. Bibcode:2012PLoSO...747143U. doi:10.1371/journal.pone.0047143. ISSN 1932-6203. PMC 3471935. PMID 23077558.
Hoops, Daniel; Weng, Hanyi; Shahid, Ayesha; Skorzewski, Philip; Janke, Andrew L.; Lerch, Jason P.; Sled, John G. (1 July 2021). "A fully segmented 3D anatomical atlas of a lizard brain". Brain Structure and Function. 226 (6): 1727–1741. doi:10.1007/s00429-021-02282-z. ISSN 1863-2661. PMID 33929568. S2CID 233459159.
^ Stuart-Fox, Devi M.; Moussalli, Adnan; Johnston, Gregory R.; Owens, Ian P. F. (2004). "Evolution of color variation in dragon lizards: quantitative tests of the role of crypsis and local adaptation". Evolution. 58 (7): 1549–1559. doi:10.1554/03-448. PMID 15341157. S2CID 9060145.
^ McClean, Claire Alice (2014). Geographic variation and speciation in the colour polymorphic tawny dragon lizard (PhD thesis). University of Melbourne. hdl:11343/39946.
^ Teasdale, T.C.; Stevens, M (2013). "Discrete color polymorphism in the tawny dragon lizard Ctenophorous descresii and differences in signal conspicuousness among morphs". Journal of Evolutionary Biology. 26 (5): 1035–1046. doi:10.1111/jeb.12115. PMID 23495663. S2CID 33168207.
^ Stuart-Fox, D.M.; Moussali, A. (2003). "Conspicuous males suffer higher predation risk". Animal Behaviour. 66 (3): 541–550. doi:10.1006/anbe.2003.2235. S2CID 11691062.
^ McFadden, Michael, and Peter S. Harlow. "Captive reproduction and longevity in Tawny Crevice (Ctenophorus decresii) and Central Netted Dragons (C. nuchalis)". HERPETOFAUNA-SYDNEY- 37.1 (2007): 22.
^ McLean, Claire A.; Moussalli, Adnan; Sass, Steve; Stuart-Fox, Devi (2013). "Taxonomic assessment of the Ctenophorus decresii complex (Reptilia: Agamidae) reveals a new species of dragon lizard from western New South Wales". Records of the Australian Museum. 65 (3): 51–63. doi:10.3853/j.2201-4349.65.2013.1600.
McFadden, Michael; Harlow, Peter (1 January 2007). "Captive reproduction and longevity in Tawny Crevice (Ctenophorus decresii) and Central Netted Dragons (C. nuchalis)". Herpetofauna. 37: 23–27.
Harlow, Peter S. (December 2000). "Incubation Temperature Determines Hatchling Sex in Australian Rock Dragons (Agamidae: Genus Ctenophorus)". Copeia. 2000 (4): 958–964. doi:10.1643/0045-8511(2000)000[0958:ITDHSI]2.0.CO;2. ISSN 0045-8511. S2CID 86330405.
Osborne, Louise (1 June 2005). "Rival recognition in the territorial tawny dragon (Ctenophorus decresii)". Acta Ethologica. 8 (1): 45–50. doi:10.1007/s10211-005-0108-6. ISSN 1437-9546. S2CID 13308856.
^ Osborne, Louise (2004). Male contest behaviour and information content of signals used by the Australian tawny dragon, Ctenophorus decresii (PhD thesis). The Australian National University. pp. xiii, 104 leaves. doi:10.25911/5D627063DA3FE.
Osborne, Louise (1 July 2005). "Information content of male agonistic displays in the territorial tawny dragon (Ctenophorus decresii)". Journal of Ethology. 23 (2): 189–197. doi:10.1007/s10164-005-0151-9. ISSN 1439-5444. S2CID 44042127.
Umbers, Kate D. L.; Osborne, Louise; Keogh, J. Scott (15 October 2012). "The effects of residency and body size on contest initiation and outcome in the territorial dragon, Ctenophorus decresii". PLOS ONE. 7 (10): e47143. Bibcode:2012PLoSO...747143U. doi:10.1371/journal.pone.0047143. PMC 3471935. PMID 23077558.
Walker, Samantha; Stuart-Fox, Devi; Kearney, Michael R. (December 2015). "Has contemporary climate change played a role in population declines of the lizard Ctenophorus decresii from semi-arid Australia?". Journal of Thermal Biology. 54: 66–77. doi:10.1016/j.jtherbio.2014.12.001. PMID 26615728.
Dong, Caroline M.; Johnston, Greg R.; Stuart-Fox, Devi; Moussalli, Adnan; Rankin, Katrina J.; McLean, Claire A. (March 2021). "Elevation of Divergent Color Polymorphic and Monomorphic Lizard Lineages (Squamata: Agamidae) to Species Level". Ichthyology & Herpetology. 109 (1): 43–54. doi:10.1643/h2020064. hdl:11343/281122. ISSN 2766-1512. S2CID 233839612.
McLean, C. A.; Moussalli, A.; Stuart-Fox, D. (2014). "Local adaptation and divergence in colour signal conspicuousness between monomorphic and polymorphic lineages in a lizard". Journal of Evolutionary Biology. 27 (12): 2654–2664. doi:10.1111/jeb.12521. ISSN 1420-9101. PMID 25330209. S2CID 31746815.