Ctenophorus spinodomus, Sadlier & Colgan & Beatson & Cogger, 2019

Sadlier, Ross A., Colgan, Don, Beatson, Cecilie A. & Cogger, Hal G., 2019, Ctenophorus spinodomus sp. nov., a New Species of Dragon Lizard (Squamata: Agamidae) from Triodia Mallee Habitat of Southeast Australia, Records of the Australian Museum 71 (5), pp. 199-215: 207-212

publication ID

http://doi.org/ 10.3853/j.2201-4349.71.2019.1700

publication LSID

lsid:zoobank.org:pub:07502465-79E0-44F2-8A51-EC4F78DE208B

persistent identifier

http://treatment.plazi.org/id/47B3F6FF-A157-4C41-8070-FFE53FD36EDF

taxon LSID

lsid:zoobank.org:act:47B3F6FF-A157-4C41-8070-FFE53FD36EDF

treatment provided by

Felipe

scientific name

Ctenophorus spinodomus
status

sp. nov.

Ctenophorus spinodomus   sp. nov. Sadlier, Colgan, Beatson & Cogger

http://zoobank.org/NomenclaturalActs/ 47B3F6FF-A157-4C41-8070-FFE53FD36EDF

Figs 5–7 View Figure 5 View Figure 6 View Figure 7

Holotype. AMS R.156615, Yathong Nature Reserve (32.5742°S 145.3828°E) NSW, G. Swan (07 October 1999) GoogleMaps   . Paratypes. AMS R   . 154827–28, Yathong Nature Reserve (32.5742°S 145.3828°E), NSW GoogleMaps   , G. Swan (12–14 October 1999); R   .156647, R. 156711, Yathong National Park (32.5869°S 145.4975°E), NSW GoogleMaps   , G. Swan (1999); R. 156704, Yathong National Park or Yarra Property (32.58°S 145.40°E), NSW GoogleMaps   , G. Swan (1999); R. 157315, Yathong Nature Reserve , 10 km NNW of Shearers Quarters (32.5864°S 145.4972°E), NSW GoogleMaps   , P. Harlow and G. Swan (07 November 1998); R   .145176–77, R. 145179, Yathong Nature Reserve (32.72°S 145.53°E), NSW GoogleMaps   , P. Harlow; R.114208–09, R.114211, R. 114213–15, Mungo National Park , 5.0 km N of SE corner (33.77°S 143.22°E), NSW, R GoogleMaps   . Sadlier and G. Shea (02 November 1984); R   . 114456–57, Mungo National Park , 5.0 km N of SE corner (33.77°S 143.22°E), NSW, R GoogleMaps   . Sadlier and G. Shea (12 November 1984); R   .114347–48, R. 114349, Top Hut Homestead , 6.9 km S on Old Arumpo Rd. (33.73°S 142.92°E), NSW, R GoogleMaps   . Sadlier and G. Shea (17 November 1984); R   . 115216, Top Hut Station , 8 km NE Roys Tank (33.68°S 142.98°E), NSW GoogleMaps   , C. Tiedermann (25 November 1984); R   . 153214–16, Warrakoo Station (33.9858°S 141.1180°E), NSW GoogleMaps   , M. LeBreton (16 October 1998); R   . 7755–76, Murray Bridge (35.12°S 139.27°E), SA GoogleMaps   ; R GoogleMaps   . 20989, Renmark (34.17°S 140.75°E), SA GoogleMaps   ; R GoogleMaps   . 145481–82 Brookfield Conservation Park (34.32°S 139.50°E), SA GoogleMaps   ; R GoogleMaps   . 104842–43, Renmark (34.17°S 140.75°E), SA GoogleMaps   .

Etymology. The species epithet is derived from a combination of the Latin spinosus for spiny and domus for home, in reference to the species’ reliance on Triodia   grass hummocks.

The common name Mallee Dragon has been applied to “ Ctenophorus fordi   ” in its broadest sense, in keeping with this concept we recommend the common name Eastern Mallee Dragon for the species described here as Ctenophorus spinodomus   sp. nov.

Diagnosis. Ctenophorus spinodomus   sp. nov. is diagnosed from all other species in the genus, except for the taxa currently contained within C. maculatus   and C. fordi   , in having a near continuous row of femoral pores either side (15–22) in adult males arranged in a row that arches forward to an apex on the midline, and a dark chest patch (although obscure) between the forelimbs in adult males. Adult female C. spinodomus   sp. nov. can be distinguished from other regionally sympatric ( C. pictus   ) or parapatric ( C. nuchalis   ) species of Ctenophorus   by the presence (vs absence) of a fine, typically uninterrupted pale dorsolateral stripe down the body from the neck to just past the hindlimbs.

Adult male C. spinodomus   sp. nov. are diagnosed from all named subspecies of Ctenophorus maculatus   in having fewer femoral pores in total (maximum 41 vs range of 40–57 encompassed by the maculatus   subspecies—Storr, 1965), and in the dark markings on the throat being present as a series of dark spots and blotches either side of the midline of varying intensity and degree of coalescence vs a pattern of well-defined narrow to broad dark bars either side.

The following features of colouration and scalation in combination distinguish Ctenophorus spinodomus   sp. nov. from taxa assignable to the other genetic lineages under C. fordi   (see Tables 2 and 3): tail length c. 2.1–2.4 times the body length in males and c. 1.95–2.15 times in females: hindlimb length c. 82–93% SVL in males, c. 74–93% in females; upper labial scales 10–13; subdigital lamellae scales 25–31; femoral pore scales in males 16–22 either side; dark markings of the throat of adult males typically obscure and present as scattered spots and blotches, occasionally aligned either side of the midline but not coalescing to form elongate blotches; chest of adult males with a typically poorly-defined black “T” shaped patch.

Comparison with other species ( Tables 2 and 3): Adult male C. spinodomus   sp. nov. are most similar to adult male aff. Group 1 ( C. aff. spinodomus   ), but differ in having shorter limbs and fewer preanal pores. Adult male and female C. spinodomus   sp. nov. have a shorter tail length on average than adult males and females from other populations referable to the C. fordi   Group 2 ( C. fordi   s.s.), Group 3 (Strzelecki) and Group 4 (GVD) genetic lineages, but with overlap in ranges. The tail length of adult male C. spinodomus   sp. nov. is similar to adult males referable to the C. fordi   Group 5 (Eyre) genetic lineage, but adult female C. spinodomus   sp. nov. have a significantly shorter tail than Group 5 females with only minimal overlap in range. The average hindlimb length of adult male and female C. spinodomus   sp. nov. is shorter than Group 2, Group 3 and Group 4 males and females but with overlap in ranges, though minimal to negligible respectively with Group 4 males and females. In scalation adult male and female C. spinodomus   sp. nov. have on average fewer subdigital lamellae than adult Group 2, Group 3 and Group 4 males and females but with overlap in ranges, though minimal with respect to Group 3 females and negligible with respect to Group 4 males and females, and adult male C. spinodomus   sp. nov. have fewer subdigital lamellae than Group 5 adult males but with overlap in range. Adult male C. spinodomus   sp. nov. have on average more femoral pore scales than Group 3 and Group 4 males with minimal to negligible overlap respectively in range, and less than Group 5 males with minimal overlap in range.

Adult male C. spinodomus   sp. nov. have a black “T” shaped chest patch which is typically poorly defined. The black chest markings of aff. Group 1 and taxa assignable to the other genetic lineages under C. fordi   are typically bold in expression and differ markedly in shape.

Description. The species is described from 17 adult males and 15 adult females regarded as representative of populations in central-west and southwest New South Wales, and southeast South Australia.

Measurements and scalation adult males: size 41.4–48.7 mm SVL (mean = 45.2); distance from axilla to groin 44.0– 52.7% SVL (mean = 47.3); head length (HDL) 20.8–25.8% SVL (mean = 23.9); head width 75.4–93.4% HDL (mean = 83.9); hindlimb length (HLL) 82.1–92.6% SVL (mean = 87.3); tail length 207.1–241.5% SVL (mean = 224.1, n = 16); upper labial scales 10–13 (mean = 12.0, sd = 0.7); lamellae beneath fourth toe 25–30 (mean = 27.8, sd = 1.8); femoral pore scales 16–22 (mean = 18.6, sd = 1.42, n = 15).

Measurements and scalation adult females: size 43.6–54.5 mm SVL (mean = 48.6); distance from axilla to groin 43.9– 53.6% SVL (mean = 48.1); head length (HDL) 20.8–25.4% SVL (mean = 23.4); head width 80.3–92.7% HDL (mean = 85.0); hindlimb length (HLL) 74.5–91.7% SVL (mean = 82.0); tail length 193.5–216.3% SVL (mean = 205.2); upper labial scales 10–13 (mean = 11.9, sd = 0.7); lamellae beneath fourth toe 25–31 (mean = 27.5, sd = 1.5).

Significant differences between adult males and adult females were found for body size* with adult females larger on average than adult males (SVL mean = 48.6 vs 45.2), for tail length* with adult males having longer tails (TL mean = 224.1 vs 205.2% SVL), and for hindlimb length* with adult males having longer limbs (HLL mean = 87.3 vs 82.0% SVL).

Colour and pattern: adult males ( Figs 5 View Figure 5 A–D, 6A, 7A)— dorsal surface in life orange-brown and defined from the lateral surface by a narrow (2 sometimes 3 scales width), pale, dorsolateral stripe with a dark edge that extends from the nape to base of the tail ending abruptly just past the hindlimbs. Dorsal surface of the body with a series of small dark blotches adjacent to and contacting the pale dorsolateral stripe and a scattering of very fine dark flecks on the top of head and body, the extent of spotting (particularly on the head) varying from sparse to moderately dense between individuals at a location. Intrapopulation variation in definition of pattern on the lateral surface is present. Upperlateral surface with a base colour similar (orange-brown) or marginally darker (mid brown) in tone to the dorsal surface, and dominated by a series of large dark markings (blackish blotches) of varying intensity and definition between the fore and hindlimbs, usually concordant in placement with the position of opposing small dark blotches on the dorsal surface of the body. Mid-lateral surface with a variably defined pale midlateral stripe along the side of the body between the fore and hindlimbs, distinct and defined by the dark markings (blotches) of the upper-lateral surface and a line of fine dark scattered spots along the upper and lower edges of the pale stripe, less well-defined in other individuals where the line of dark makings along the upper and lower edges of this stripe are not continuous and present only as scattered flecks. Lower surface with similar colouration to upper-lateral surface, but with the base colour tending to border the lower edge of the pale midlateral stripe and the darker markings the lateroventral margin. Tail similar in colour above to the dorsal surface of the body. The pale dorsolateral stripe of the body continues a third or less of the way along the tail as a series of faint pale spots scattered along the dorsolateral edge. Side of tail uppermost dark (an extension of the dark upper lateral markings of the body) and tending to form a distinct stripe, which in turn is bordered below by a pale stripe (an extension of the pale midlateral stripe of the body) for approximately the basal third of the tail, which in turn is defined for most of its length from the underside of the tail by a series of fine dark markings along the ventrolateral margin, usually continuous along most of its length and forming a fine dark stripe.

Ventral surface pale, white in life, with dark scattered markings on the throat and chest. Dark throat markings variable in distribution and intensity, sometimes sparse and scattered but also tending to align either side of the midline, and only rarely forming narrow and elongate blotches which approach each other towards the chin. Dark chest markings also variable in distribution and intensity, sometimes presents as a few blotches medially between the forelimbs through to being aligned to form a poorly defined “T”-shaped patch with the lateral extensions typically narrow but the rearward extension varying from narrow to occasionally broad. Most individuals with a narrow alignment of dark markings along the anterior ventrolateral edge of the forelimbs, sometimes present as a continuous stripe at least on the humerus.

Adult females ( Figs 5 View Figure 5 E–F, 6B, 7B)—dorsal and lateral surface with a similar pattern to males but overall lighter in tone. Ventral surface with the dark throat markings present as greyish specks and smudges, and chest typically without areas of dark markings.

Variation. No significant difference in scalation or body proportions were detected between populations from centralwest NSW and those from southwest NSW, or with those from southeast SA west of the Murray River.

Distribution and biology. Ctenophorus spinodomus   sp. nov. occurs on the red sandplains belonging to the Mallee dunefields (as identified by Hesse, 2010) of central-west and southwest NSW and adjacent areas of inland southeast SA that lie to the north and west of the main Murray River channel, within the IBRA bioregions of the Murray-Darling Depression (with the exception of the Darling Depression subregion) and Cobar Peneplain bioregions. Here, the distribution of populations in central-west and southwest NSW is dependent on the presence of Triodia   hummock grass which grows as a groundcover in association with mallee woodlands ( Cogger, 1974; Sadlier & Shea, 1989), termed Triodia Mallee habitat   ( Fig. 8 View Figure 8 ). Extensive information on the species biology has been published by Cogger (1974, 1978) based on population studies undertaken at Round Hill Nature Reserve in centralwest NSW. We present here a summary of points relevant to its reliance upon this habitat type and vulnerability to decline. The population referred to as C. aff. spinodomus   occurs in adjacent areas of northwest Victoria to the south and east of

the major “Groups”. the main Murray River channel within the Mallee dunefields, and the extent of reliance of these populations on Triodia Mallee habitat   has yet to be established.

Ctenophorus spinodomus   sp. nov. has an essentially annual life cycle, with some individuals extending into a second, rarely a third, season. Marked mortality of adults begins in late December and extends into January, with a loss of up to 85% of the population. Densities approaching 125 individuals per hectare have been found in areas regenerated 5–10 years after fire, but climax mallee communities with well-developed Triodia   have lower densities. Males have a larger home range (mean 0.032 ha) than females (mean 0.015 ha), with juveniles a smaller range (0.007 ha) than adults, but with little shift in home range and negligible migration, and no territorial behaviour has been recorded ( Cogger, 1978).

The species diel cycle revolves around utilization of Triodia   clumps at various times of the day. During the night individuals shelter within Triodia   and undergo preemergence basking amongst the spines of the clump to attain a body temperature sufficient for activity. On emergence individuals have not been observed active more than a few metres from the nearest clump of Triodia   . During the hottest part of the day most lizards retire within the clumps of Triodia   where summer humidity levels are higher than ambient and temperature during the hottest part of the day markedly lower than ambient and more so than substrate. However, during the winter period few individuals were found residing inactive within Triodia   , rather, opportunistic observations suggest they dig into soil and shelter underground, but not in specially constructed burrows. It feeds almost exclusively on small ants but will take other insects opportunistically.

The earliest recorded egg-laying in Round Hill was mid- October and the latest in late January, with a peak period for egg deposition around mid-November. Development of a clutch of eggs takes less than 8 weeks. Females deposit 2– 3 eggs in a chamber that is constructed and sealed on the same day after laying. No female was recorded laying more than two clutches in a season, but given the clutch development period and length of laying season three clutches could be achieved. On average only 20% of hatchlings survive to reproductive age in the Round Hill population.

Comments. Wells & Wellington described Phthanodon hawkeswoodi   sp. nov. in 1985. The designated holotype is a specimen (AMS R.116983) from Glenlea central fire trail Yathong Nature Reserve, NSW (collector A. B. Rose and J. Brickhill, 14 March 1981). The diagnosis presented by Wells & Wellington amounts to an extended description of the holotype that failed to provide either a “… definition that states in words characters that are purported to differentiate the taxon” or a “… bibliographic reference to such a published statement… ”, as required under Article 13(a)(i–ii) of the Third edition of the Code of Zoological Nomenclature applicable at that time. As such, the description of Phthanodon hawkeswoodi Wells & Wellington, 1985   is unavailable for application to the species described here as C. spinodomus   sp. nov.

Houston (1978) identified three distinct races of what was then considered Amphibolurus fordi in SA. One   of these, his “eastern” race, was mapped as being from far southeast

the major “Groups”.

SA, and by implication continuous with populations of C. spinodomus   sp. nov. in southwest NSW. His “Eyre Peninsula” race corresponds   to our Group 5 fordi   genetic lineage from Eyre Peninsula, however, his “northern” race which   included all other populations in the north and west of the state, was a composite of the Group 3 fordi   genetic lineage from the Strzelecki and Tarari desert systems and the Group 4 fordi   genetic lineage from the Great Victoria Desert.

Edwards et al. (2015) figured the distribution of populations from northwest Victoria and far southeast SA (their C. fordi   clade 5) as extending west across the Murray River and bisecting the Group 1 populations in southeast SA and southwest NSW. Reference to the online supplementary data for this publication gives one specimen (listed as 40887) with the coordinates “-34.05 139.1833”, which would place it west of the Murray River. Presumably this is the South Australian Museum specimen R40887 View Materials which is listed in the museum database as from Morgan Conservation Park, and with those same coordinates. However, Morgan Conservation Park lies 50 km to the east of these coordinates and on the south and east side of the Murray River. On the assumption the coordinates used to map this specimen are in error, all populations identified by Edwards et al. as belonging to their C. fordi   clade 5 genetic lineage actually lie entirely to the south and east of the main Murray River channel, and the distribution of this lineage is parapatric to (not bisecting) the C. spinodomus   sp. nov. populations in southeast SA and southwest NSW—a result consistent with our morphological investigations.

R

Departamento de Geologia, Universidad de Chile

NSW

Royal Botanic Gardens, National Herbarium of New South Wales

SA

Museum national d'Histoire Naturelle, Laboratiore de Paleontologie