Conservation Advice and Transferred This Species from the Endangered to Vulnerable Category, Effective from 04/07/2019

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Conservation Advice and Transferred This Species from the Endangered to Vulnerable Category, Effective from 04/07/2019 THREATENED SPECIES SCIENTIFIC COMMITTEE Established under the Environment Protection and Biodiversity Conservation Act 1999 The Minister approved this conservation advice and transferred this species from the Endangered to Vulnerable category, effective from 04/07/2019 Conservation Advice Litoria dayi (Lace-eyed Tree Frog) Taxonomy Conventionally accepted as Litoria dayi (Gunther 1897). Litoria dayi (Lace-eyed Tree Frog) was recently transferred to the genus Litoria from the genus Nyctimystes after Kraus (2013) showed that it did not meet the morphological characteristics for assignment to that genus (Cogger 2014). Summary of assessment Conservation status Vulnerable: Criterion 2 B1 and B2 (a),(b)(i,ii) The highest category for which Litoria dayi is eligible to be listed is Vulnerable. Litoria dayi has been found to be eligible for listing under the following categories: Criterion 2: B1 and B2 (a),(b)(i,ii): Vulnerable Litoria dayi has been found to be eligible for listing under the Vulnerable category. The species was eligible for listing under the Environmental Protection and Biodiversity Conservation Act (1999) (EPBC Act) as on 16 July 2000 it was listed as Endangered under Schedule 1 of the preceding Act, the Endangered Species Protection Act 1992 (Cwlth). Following a formal review of the listing status of the Lace-eyed Tree Frog, the Threatened Species Scientific Committee (the Committee) has determined that there is evidence that the species has stabilised but has not undergone any demonstrable recovery since being listed; and that there is sufficient evidence to support a change of status of the species to Vulnerable under the EPBC Act but not to delist the species. Therefore, the Committee concluded that the listing status of the Lace-eyed Tree Frog should be changed to Vulnerable under the EPBC Act. Species can be listed as threatened under state and territory legislation. For information on the listing status of this species under relevant state or territory legislation, see http://www.environment.gov.au/cgi-bin/sprat/public/sprat.pl Reason for conservation assessment by the Threatened Species Scientific Committee This advice follows assessment of new information provided to the Committee to reassess the listing status of Litoria dayi for potential delisting and the subsequent finding that the listing status of the species should be changed from Endangered to Vulnerable. The information contained in this Conservation Advice was sourced from the ‘Recovery plan for the wet tropics biogeographic region of north-east Queensland 2000 - 2004 (Northern Queensland Threatened Frogs Recovery Team 2001) and various scientific papers and reports. Litoria dayi (Lace-eyed Tree Frog) Conservation Advice Page 1 of 13 Relevant part of the EPBC Act for amending the list of threatened native species Section 186 of the EPBC Act states that: “(2A) The Minister must not delete (whether as a result of a transfer or otherwise) a native species from a particular category unless satisfied that: (a) the native species is no longer eligible to be included in that category; or (b) the inclusion of the native species in that category is not contributing, or will not contribute, to the survival of the native species.” Public consultation Notice of the proposed amendment and a consultation document was made available for public comment for 31 business days between 17 January 2018 and 2 March 2018. Any comments received that were relevant to the survival of the species were considered by the Committee as part of the assessment process. Species Information Description This species is a small to medium sized frog growing to 50 mm in snout-to-vent length. The dorsal surface is rich-brown to orange-brown with or without scattered cream or lichen like spots and blotches, sometimes with black centers, covering it, the head or the limbs. The skin is smooth or finely granular above, coarsely granular on the lower flanks and ventral surfaces. The limbs often have faint banding or marbling and a slight fringe along the outer edges. The belly is cream-white or yellowish, with the throat and under surface of the thighs being blackish. The eyes are large and prominent with a dark brown iris. The lower eyelid is patterned with lines, veins and dots which give the frog its name. Fingers are almost completely webbed. Toe discs are usually smaller than finger discs. The tympanum is indistinct or hidden, although the tympanic annulus is usually distinct (Czechura et al. 1987; Cogger 2014). In chorus, the mating call is a drawn out "eeeeeeeee" that inflects downwards at the end, repeated three or four times in succession, producing a harsh growl-like sound. Solitary males can produce a short, sharp "ee" every five to six seconds, sometimes over long periods (Czechura et al. 1987; McDonald 1992). Females may lay over a 100 large (2.3-2.6 mm diameter) unpigmented eggs with discrete egg capsules in a cohesive clump on or under rocks in water or just above the water-line (Czechura et al. 1987; Davies & Richards 1990). The tadpole has a body form that is adapted for living in fast flowing streams. The head and body are flattened, dark brown above, a sandy colour ventrally. The tail is very muscular, with distinct dark and light patches. The tail fins are arched and rounded terminally, transparent with irregular pigmentation. They feature a suctorial oral- disc, larger than those found in tadpoles of the L. nannotis group. Distribution The Lace-eyed Tree Frog is endemic to the Wet Tropics Bioregion from Paluma to Cooktown, northern Queensland, at altitudes between sea level and 1200 m above sea level (asl) (Williams & Hero 1998; 2001). Before its decline, the extent of occurrence of this species was approximately 9000 km² (McDonald 1992). The Lace-eyed Tree Frog has disappeared from upland sites throughout the Wet Tropics and was last recorded from Mount Spec State Forest in 1990 and the Kirrama Range in 1989 (Richards et al. 1993). Following a survey over the summer of 1991-1992 Richards et al. (1993) noted that the species was still common at most foothill and lowland sites and recorded adults and larvae from upland sites north of the Daintree River. These populations subsequently disappeared in 1992 and 1993 (M. Cunningham pers. comm.). At one monitoring site at O’Keefe Creek, Big Tableland, this species had been known to occasionally reappear near a site at an Litoria dayi (Lace-eyed Tree Frog) Conservation Advice Page 2 of 13 altitude of 400 m asl, but it did not establish resident populations and was absent from a monitoring site at 680 m asl (McDonald & Alford 1999). However, populations have been persisted in the lowlands and foothills (McDonald & Alford 1999; Northern Queensland Threatened Frogs Recovery Team 2001; Hodgkinson & Hero 2003; Phillott & Young 2009; Phillott et al. 2010). Survey results from 1991 found the species was occurring in the Wet Tropics World Heritage Area (where there is no logging or clearing of its habitat), in Cedar Bay National Park, Crater Lakes National Park, Daintree National Park, Lumholtz National Park, Millstream National Park, Paluma Range National Park and Wooroonooran National Park, Crystal Cascades National Park, Wallaman Falls (Seaview), and Palmerston National Park, and Daintree Timber Reserve (165 Monkhouse) as well as Lamb Range, Mt Lewis, Mt Spec and Windsor Tableland State Forests (SF 768 Alcock) (Tyler 1997; M.Cunningham 2001, pers. comm). However, more recent surveys indicate that they are completely extirpated from the southern extent of their range and are no longer found at Paluma Range National Park (Bower et al. 2018; McKnight et al. 2017). In the field, stable populations of several species susceptible to the amphibian chytrid fungus (including the Lace-eyed Tree Frog) persist at lower altitudes where temperatures are higher compared to highland sites (McDonald & Alford 1999). Recent surveys on Lace-eyed Tree Frog (2015–2017) found that although populations persist, and were even found to be abundant at some lowland sites at altitudes where temperatures are higher compared to highland sites (McDonald & Alford 1999; McKnight et al. 2017), the species has not recovered or formed any new populations in the survey area (Bower et al. 2018). The existing populations are relatively small compared to pre-chytridiomycosis numbers and vulnerable to any changes in environment because they lack a diversity of habitat that would allow the species to respond to other threats. Further, it is possible that they lack the genetic diversity necessary to respond to threats, such as new or emerging pathogens. Relevant Biology/Ecology This species is a rainforest specialist. In montane areas the species prefers fast-flowing rocky streams although they also frequent slower watercourses where ample vegetation exists along the margins (Czechura et al. 1987). At low elevations, the species favours rock soaks, narrow ephemeral streams and rock outcrops in larger watercourses, and it may also be found on rocks, boulders and vegetation in or adjacent to streams (Czechura et al. 1987). They are dependent on rainforest vegetation, inhabiting complex, densely vegetated habitats. Females move considerable distances (up to 50 m) from streams (Rowley & Alford 2009). Adults feed on both aquatic and terrestrial invertebrates (Hodgkinson & Hero 2003). Their principal diet includes Coleoptera, Aranea, Odonate larvae, Blattodea and Diptera (Hodgkinson & Hero 2003). The Lace-eyed Tree Frog is a spring/summer breeder (Davies & Richards 1990) with peak breeding activity from October to April. Tadpoles from eggs laid in early summer complete development in 3-4 months, whereas tadpoles from eggs laid in late summer may over-winter and metamorphose the following summer. During the early stages of development, tadpoles from a single clutch aggregate together under a single rock. This behaviour persists until the gut is fully formed, after which they disperse and commence grazing on algal-covered rocks.
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