© The Authors, 2009. Journal compilation © Australian Museum, Sydney, 2009 Records of the Australian Museum (2009) Vol. 61: 39–48. ISSN 0067-1975 doi:10.3853/j.0067-1975.61.2009.1518 New Records of Plio-Pleistocene Koalas from Australia: Palaeoecological and Taxonomic Implications Gilbert J. Price1*, Jian-xin Zhao1, Yue-xinG FenG1 and Scott a. hocknull2 1 Radiogenic Isotope Facility, Centre for Microscopy and Microanalysis, The University of Queensland, St. Lucia 4072 Queensland, Australia [email protected] 2 Geosciences, Queensland Museum, 122 Gerler Road, Hendra 4011 Queensland, Australia abStract. Koalas (Phascolarctidae, Marsupialia) are generally rare components of the Australian fossil record. However, new specimens of fossil koalas were recovered during recent systematic excavations from several eastern Plio-Pleistocene deposits of Queensland, eastern Australia, including the regions of Chinchilla, Marmor and Mt. Etna. The new records are significant in that they extend the temporal and geographic range of Plio-Pleistocene koalas from southern and southeastern Australia, to northeastern central Queensland. We provide the first unambiguous evidence of koalas in the Pliocene Chinchilla Local Fauna (phascolarctid indet. and Ph. ?stirtoni): important additions to an increasingly diverse arboreal mammalian assemblage that also includes tree kangaroos. The persistence of koalas and local extinction of tree kangaroos in the Chinchilla region today suggests that significant habitat and faunal reorganization occurred between the Pliocene and Recent, presumably reflecting the expansion of open woodlands and grasslands. Other koala records from the newly U/Th-dated Middle Pleistocene Marmor and Mt. Etna fossil deposits (Phascolarctos sp. and Ph. ?stirtoni), along with independent palaeohabitat proxies, indicate the former presence of heterogeneous habitats comprised of rainforests, open woodlands and grasslands. The lack of such habitat mosaics in those regions today is likely the product of significant Middle Pleistocene climate change. Price, Gilbert J., Jian-xin Zhao, Yue-xinG FenG and Scott a. hocknull, 2009. New records of Plio-Pleistocene koalas from Australia: palaeoecological and taxonomic implications. Records of the Australian Museum 61(1): 39–48. Koalas (Phascolarctidae, Marsupialia) are Australian separated from all other vombatiformes (i.e., wombats, endemic, relatively large-sized (c. 10 kg), arboreal marsupials marsupial “lions”, illarids, wynyardiids, maradids, and that occupy a similar ecological niche to placental lemuroids diprotodontoids) on the basis of their selenodont dental or sloths (Murray, 1984). The modern Koala, Phascolarctos morphology and occupy a position near the base of the cinereus, is the only surviving member of an ancient and diprotodontian ordinal tree (Archer, 1976; Archer & diverse family of marsupials, with the oldest members Hand, 1987). A recent molecular phylogeny supermatrix, known from the Late Oligocene (Black, 1999). Six to temporally-constrained using dated occurrences of fossil seven genera and 18 species (several undescribed) are taxa, suggested that koalas diverged from vombatoids currently recognized (Black, 1999). Phascolarctids are during the Middle Eocene (Beck, 2008). * author for correspondence 40 Records of the Australian Museum (2009) Vol. 61 Koalas are generally rare components of the Australian the true age of initial calcite crystallization. However, in fossil record, presumably reflecting their arboreal habits this dating study, the calcite precipitated within long bone (Murray, 1991), and fossil koala material is commonly hollows at some stage after deposition, thus, the calculated fragmentary and/or poorly preserved. Thus, determination U/Th ages will represent minimum ages for the associated of intra- and interfamilial phascolarctid relationships has faunal assemblages. proven difficult. Pre-Holocene koalas are known from Oligo- Fresh bone and teeth contains little or no U. However, Miocene deposits of Riversleigh, Frome Basin, and Tirari after burial, U is taken up from the environment by bone Desert (Stirton et al., 1967; Woodburne et al., 1987; Black apatites that scavenge U, but exclude Th, during diagenesis. & Archer, 1997; Myers et al., 2001; Louys et al., 2007); Late Unlike speleothem, bones and teeth are open systems for Miocene-Pliocene deposits of Corra Lynn Cave and Waikerie U (Grün et al., 2008), therefore, the U/Th dates commonly (Pledge, 1987); and Pleistocene deposits of Koala Cave, represent the mean age of U-uptake history. Thus, a Mammoth Cave, Devil’s Lair, Tight Entrance Cave, Lake calculated age most likely represents a minimum age for the Eyre region, Madura Cave, Lake Menindee, Lake Victoria, dated bone or tooth. This has previously been demonstrated Nelson Bay, Naracoorte region, Wellington Caves, and Gore for eastern Australian cave deposits where U/Th dating (Bartholomai, 1968; Merrilees, 1968; Archer, 1972; Balme of deposit-capping speleothem (thus, also representing et al., 1978; Lundelius & Turnbull, 1982; Tedford & Wells, minimum ages) return dates that are always older than U/ 1990; Archer et al., 1997; Dawson & Augee, 1997; Moriarty Th dated bone and teeth recovered from within the deposit et al., 2000; Reed & Bourne, 2000; Piper, 2005; Ayliffe et itself (Hocknull et al., 2007). al., 2008; Price, 2008a) (Fig. 1). The koala fossil record Unfortunately, U/Th datable material that could from the central to north eastern margin of the Australian potentially produce maximum ages of deposition was not continent is particularly depauperate, with only one specimen recovered from the Marmor and Mt. Etna koala deposits. known (type specimen of Phascolarctos stirtoni from Gore, No dateable samples were obtained from the Chinchilla southeast Queensland). Koobor, a koala-like vombatiform fossil deposits. marsupial is also known from isolated specimens from the Bluff Downs (central eastern Queensland) and Chinchilla Terminology. Dental nomenclature follows Luckett (1993) Local Faunas (southeastern Queensland (Archer & Wade, where the adult unreduced cheek tooth formula of marsupials 1976; Archer, 1977a). Although originally considered to be is P1–3 and M1–4 in both upper and lower dentitions. Dental a koala, more recent morphology-based phylogenic analyses cusp terminology follows Archer (1978) except for what suggest that Koobor sits outside the Phascolarctidae (Black was then interpreted to be the hypocone, is now regarded & Archer, 1997) and may actually be a primitive sister-group to be the metaconule, based on its linkage through the of wynyardiids and ilariids (Myers & Archer, 1997). postprotocrista with the protocone and metacone (Tedford Here we report new specimens of fossil koalas that were & Woodburne, 1987; Tedford & Woodburne, 1998). Higher- recovered during recent systematic excavations from several level systematic nomenclature follows Aplin & Archer Plio-Pleistocene deposits of eastern Queensland, including (1987). All measurements were made using callipers and the regions of Chinchilla, Marmor and Mt. Etna (Fig. 1). are given in millimetres (mm). Although the new specimens are fragmentary, the paucity of information about koalas in the Plio-Pleistocene makes Institutional abbreviations. QMF, Queensland Museum the new eastern Australian material particularly noteworthy. Fossil specimen, Queensland Museum, Brisbane, Australia; Thus, the aim of this paper is to describe the new material QMJ, Queensland Museum modern specimen, Queensland and discuss the taxonomic and palaeoecological implications Museum, Brisbane, Australia; QML, Queensland Museum within a reliable geochronological framework. fossil Locality, Queensland Museum, Brisbane, Australia; SAMP, South Australian Museum Palaeontological Materials and methods specimen, South Australian Museum, Adelaide, Australia. Dating. Samples of bone and post-depositional calcite Geographic and geological settings growth within long-bone hollows from the Marmor and Mt. Etna cave fossil deposits were targeted for thermal ionization Chinchilla. Site QML7 is located in Chinchilla, south- mass spectrometry (TIMS) U/Th dating. Each sample eastern Queensland (Fig. 1). Vertebrate fossils, constituting was pre-treated and processed at the Radiogenic Isotope the Chinchilla Local Fauna, are predominantly derived Facility, The University of Queensland, following techniques from the Chinchilla Sand, a lithostratigraphic sequence described in Zhao et al. (2001) and Yu et al. (2006). of fluviatile sediments exposed in the Condamine River Speleothem calcites and aragonites are secondary between Nangram Lagoon and Warra (Woods, 1960). mineral deposits that form in cave environments. Uranium The Chinchilla Sand includes well-lithified calcareous is commonly leached from downward percolating meteoric sandstones grading into siltstone and conglomerate (quartz waters and becomes co-precipitated within speleothem and ferruginous sandstone), and weakly consolidated calcite (or aragonite) during genesis. At the time of sands that grade into silt and sandy clay. Such sediments speleothem formation, some U, but little or no Th, is were derived from erosion of the Orallo Formation and its incorporated into the calcite (or aragonite) lattices, and lateritized profiles (Bartholomai & Woods, 1976). There disequilibrium in the U-series decay chain occurs. The U/ are no analytical dates associated with the Chinchilla Sand. Th age is calculated by determining the amount of 230Th However, biochronological correlation based on fossil that was produced by the decay of 238U (via intermediate vertebrates to other important radiometrically-dated faunas isotope 234U). Thus, dating of speleothem material provides from elsewhere in Australia (e.g., Kanunka Local Fauna, Price et al.: koala palaeoecology 41 Systematic Palaeontology Super cohort Marsupialia Cuvier, 1817 Order Diprotodontia Owen, 1866 Suborder Vombatiformes Woodburne, 1984 Infraorder Phascolarctomorphia Aplin & Archer, 1987 Family Phascolarctidae Owen, 1839 Phascolarctidae gen. et sp. indet. Figs 2, 3A Referred material. QMF52287, left dentary fragment, QML7, Chinchilla, southeast Queensland, Australia (Pliocene). Description. Dentary fragment with horizontal ramus broken Fig. 1. Oligocene-Pleistocene fossil localities where koalas have anterior to P alveolus and posterior to M alveolus; surface been recovered, including present study sites (Chinchilla, Marmor 3 3 and Mt. Etna). Shaded area indicates historic (i.e., post-European bone slightly root-etched; cheek teeth crowns missing, roots settlement in Australia) geographic range of the modern Koala, present, alveolar border broken buccally; ventral border Phascolarctos cinereus. slightly in-turned lingually; mental foramen anteroventral to P anterior alveolus; posterior mental foramen well 3 developed, ventral to position between posterior root of M 1 and anterior root of M ; symphysis strongly fused, very deep, 2 Bluff Downs Local Fauna, and Hamilton Local Fauna), extended posteriorly to below posterior root of M , kinked 1 suggests a Middle Pliocene age (Whitelaw, 1991; Tedford such that posteroventral border extends below ventral border et al., 1992; Mackness et al., 2000). of horizontal ramus, inclined posteriorly at posteroventral margin, inclined anteriorly at a low angle (35°); genial pit, Marmor. Site QML1420 is located in Marmor, central c. 3 mm largest diameter, present at posterior ventral portion eastern Queensland (Fig. 1). QML1420 is a brecciated of symphysis, similar symmetrical but broken pit present on limestone cave deposit, with sediments dominated by grey opposing dentary. to brown clays and limestone clasts (Hocknull, 2005). The deposit contains typical Pleistocene megafauna including Remarks. The dentary fragment is considered to be adult Diprotodon optatum, Thylacoleo carnifex and Macropus based on the presence of well-developed P and M alveoli, 3 3 giganteus titan (Longman, 1925) (D. optatum and M. g. and a strongly fused symphysis. The dentary resembles titan taxonomy up-dated following Price (2008b) and phascolarctids in general morphology. However, QMF52287 Dawson & Flannery (1985), respectively). Direct U/Th does not appear to be referable to any phascolarctid where dating based on teeth from such taxa returned minimum ages the dentary is known. It differs from Nimiokoala, Perikoala, of 122–154 ka (Table 1) suggesting that the assemblage is Madakoala, and Phascolarctos cinereus by: (a) being Middle Pleistocene or older. The assemblage lacks faunal significantly more robust in terms of depth and width (Fig. elements typical of Pliocene assemblages and on the basis of 3A); (b) possessing a more anteriorly positioned posterior biocorrelation to nearby well-dated deposits of the Mt. Etna mental foramen; (c) having a straighter ventral border; region (Hocknull et al., 2007), site QML1420 is unlikely to and (d) by possessing a relatively deeper symphysis that be older than Middle Pleistocene. has a lower anterior ascending angle. QMF52287 is more gracile in comparison to Cundokoala yorkensis (a genus Mount Etna. Site QML1384 (Unit “L.U.”; Elephant Hole that is questionably distinct from Phascolarctos; see Black, Cave) is located at Mt. Etna, central eastern Queensland 1999) (Fig. 3A), but like Ph. cinereus, also differs from (Fig. 1). It is a brecciated limestone cave deposit, with the former taxon in having a more anteriorly positioned sediments dominated by red/yellow/grey clays with posterior mental foramen, straighter ventral border, and occasional gravel and cobbles (Hocknull, 2005). Direct U/ deeper symphysis. The dentary of Litokoala is unknown, but Th dating based on a macropod bone provided an age of on the basis of alveoli dimensions, is probably significantly 267±5.2 ka (Table 1). However, due to unknown rates of U smaller than QMF52287. QMF52287 differs from Perikoala uptake, the date should be regarded as a minimum age only. and Madakoala in that the symphysis is more strongly This interpretation is supported by U/Th dating of calcite fused, and the diastema is relatively longer. Well-developed recovered from the hollow of long bone, which returned symmetrical genial pits are present at the posteroventral an age of 331.6±14 ka (Table 1). This age is likely to be base of the symphysis of QMF52287, but are not expressed closer to, but still younger than, the true age of the fossil as strongly in other koala genera. Well-developed genial assemblage. A maximum age has not been determined for pits occur in wombats such as Vombatus, but such pits are QML1384 “L.U.”, but based on faunal similarities to other relatively larger, positioned relatively higher from the ventral dated sequences in the region, the deposit is unlikely to be border, and the pits commonly converge on each other on older than 500 ka (Hocknull et al., 2007). the left and right side of the symphyseal fusion forming a 42 Records of the Australian Museum (2009) Vol. 61 Fig. 2. Phascolarctid gen et sp. indet. dentary (QMF52287) from site QML7, Chinchilla, eastern Australia. (A) External view, (B) Internal view, and (C) Occlusal view. Price et al.: koala palaeoecology 43 Fig. 3. Morphometrics of fossil koala specimens. (A) Depth versus width of dentaries of modern Phascolarctos cinereus from eastern Queensland (Appendix), fossil Cundokoala (?Ph.) yorkensis (SAMP24904) from Corra Lynn Cave (South Australia), and phascolarctid gen et. sp. indet (QMF52287) from Chinchilla, eastern Australia. Note that the depth of the Chinchilla koala dentary is a minimum measurement because the specimen is broken along the alveolar border (Fig. 2). (B) Anterior versus posterior width of Phascolarctos spp. M2 (See Appendix for list of modern Ph. cinereus specimens examined). Phascolarctos sp. Figs 3B, 4A single large pit. Comparison of QMF52287 to other large- Referred material. QMF52288, isolated LM2, QML1384 sized phascolarctids such as Ph. maris, or unusual koala-like (Unit “L.U.”; Elephant Hole Cave), Mt. Etna, central eastern marsupials such as Koobor, is not possible because dentaries Queensland, Australia (Middle Pleistocene; Table 1) of those taxa are unknown. Description. LM2 with anterior portion missing; tooth trapezoidal in occlusal outline, tapering posteriorly; Genus Phascolarctos Blainville (1816) protocone and paracone sub-equal in height, slightly taller than metacone and metaconule, neometaconule shortest Diagnosis. Upper molars of Phascolarctos differ from all cusp; protocone most anterior cusp forming anterolingual other phasco larctids (excepting Cundokoala (?Ph.) york­ corner of tooth; paracone transverse, slightly posterior to ensis) and the koala-like Koobor by: (a) being larger; (b) being protocone, forming anterobuccal margin of tooth; metacone relativel y higher crowned; (c) by possessing well-developed directly posterior to paracone forming posterobuccal corner molar crenulations; and (d) possessing well-developed ribs of tooth; metaconule posterobuccal to protocone, transverse on lingual portion of paracone and metacone. to metacone, forming posterolingual corner of tooth; Phascolarctos differs from Madakoala, Nimiokoala postprotocrista well developed, descends posterobuccally and Koobor by possessing a lingual cingulum or pocket on from apex of protocone to meet with premetaconulecrista; upper molars at the crown base between the protocone and cristae on paracone missing; rib descends posteriorly metaconule. from apex of paracone to mid-crown basin; premetacrista Phascolarctos differs from Litokoala and Nimiokoala well developed, descends anterobuccally from apex of by possessing relatively smaller neometaconules and metacone, terminating at stylar cusp D; postmetacrista well paraconules. defined, descends posterobuccally from apex of metacone; Phascolaractos differs from Madakoala, Perikoala, posterolingual crista weakly-expressed descending from Cundokoala and Koobor by possessing relatively smaller metacone apex to posterolingual base of metacone; or weakly expressed stylar cusps, and in the case of neometaconule small, distinct at anterolingual base of Cundokoala, by possessing a relatively less-developed metacone; premetaconulecrista well developed, descends associated stylar shelf. anterobuccally from apex of metaconule terminating at Phascolarctos differs from Cundokoala in being smaller midcrown basin; postmetaconulecrista well developed, and by possessing lesser-developed molar crenulations. descends posterobuccally from apex of metaconule, Phascolarctos differs from Koobor by: (a) having a with inflexion at posterior cingulum; lingual cingulum square- to trapezoidal-shaped, rather than rectangular- moderately developed at base of crown between protocone shaped, occlusal outline; (b) possessing relatively longer and metaconule; posterior cingulum well defined, descends anterior and posterior cingula; and (c) lacking a buccal from inflexion with postmetaconulecrista, terminating at ectoloph on the paracone. posterobuccal corner of tooth near stylar cusp E; metacone 44 Records of the Australian Museum (2009) Vol. 61 buccal ridge small, descends posteriorly from stylar cusp D, well developed, extending along lingual margin at base of terminating at posterobuccal corner of tooth; molar enamel protocone, ascending and terminating at lingual corner of heavily crenulated. tooth; molar enamel crenulated on all sides of protocone. Remarks. QMF52288 is regarded as an M2 due to its Remarks. The wear pattern on the posterior margin of the trapezoidal occlusal outline that tapers posteriorly and by metacone molar fragment (QMF52289) is consistent with its possession of a relatively small neometaconule, identical wear from abrasion with a succeeding tooth whilst still in to that of M2 in other species of Phascolarctos. QMF52288 the maxilla. This suggests that the specimen represents either is significantly larger than corresponding teeth of Koobor, an M1, 2 or M3, rather than an M4 (the most posterior tooth in Madakoala, Perikoala, Nimiokoala and Litokoala, and Ph. phascolarctids). On the basis of molar morphology, the teeth cinereus. However, the tooth is morphologically similar to are referable to Phascolarctos due to: (a) their well-developed other species of Phascolarctos. In comparison to Ph. stirtoni, molar crenulations; (b) minor degree of development of stylar the posterior cingula is relatively smaller, molar enamel is cusps and associated stylar shelf (QMF52289); (c) well- less crenulated (although that feature may be slightly variable developed lingual cingulum (QMF52290); and (d) being judging from variation expressed in large samples of modern higher-crowned than all other phascolarctids (excepting Ph. cinereus), and the tooth is smaller overall (Fig. 3B). Cundokoala (?Ph.) yorkensis). Morphometrically, both teeth However, judging by the range of morphometrical variation are larger than corresponding teeth of Ph. cinereus, but are exhibited in modern Ph. cinereus (Fig. 3B), QMF52288 smaller than corresponding teeth of C. (?Ph.) yorkensis. could easily fall within the lower size range of Ph. stirtoni. The protocone fragment (QMF52290) is morphologically QMF52288 is somewhat similar in morphology to extant similar to the corresponding M2 of Ph. stirtoni, particularly Ph. cinereus. However, it is larger and falls outside the in the development of the anterior fossette at the base of the morphometrical range of variation of modern populations protocone, and the anterolingual extension of the lingual (Fig. 3B). Pledge (1987) suggested that Ph. maris (a species cingulum. The metacone fragment (QMF52289) lacks a well- questionable distinct from Ph. stirtoni; see Black, 1999) is developed stylar shelf as exhibited in C. (?Ph.) yorkensis, intermediate in size between the smaller Ph. cinereus and and in that respect, closely resembles the condition exhibited larger Ph. stirtoni. Thus, QMF52288 potentially represents in Ph. stirtoni. Corresponding teeth of Ph. maris and C. (?Ph.) Ph. maris. However, it is not possible to compare QMF52288 yorkensis are either not known or are poorly represented, thus, to Ph. maris (nor to the significantly larger Cundokoala preventing further comparison to the material described here. (?Ph.) yorkensis) as corresponding teeth are unknown in However, the molar fragments described here are similar those species. in size to Ph. stirtoni, a species that is intermediate in size between Ph. maris and C. (?Ph.) yorkensis (Pledge, 1987, Phascolarctos stirtoni Bartholomai, 1968 1992). Thus, QMF52289 and QMF52290 are unlikely to be referable to those poorly known taxa. The fragmentary Holotype. QMF5707, right maxillary fragment with P3, nature of the material precludes additional comparison to M1–2, Cement Mills, Gore, southeastern Queensland (Late Ph. stirtoni. Pleistocene; Price et al., 2009). Discussion Diagnosis. See Bartholomai (1968). New koala material described here significantly extends the temporal and spatial distribution of Plio-Pleistocene koalas Phascolarctos ?stirtoni in Australia. Previously, Pliocene records of koalas were Figs 4B, C restricted to southern Australian deposits (i.e., Corra Lynn Cave and Waikerie). Thus, the new records from the Chinchilla Referred material. QMF52289, isolated RM1, 2 or 3 fragment, Local Fauna (phascolarctid indet. and Phascolarctos ?stirtoni) QML7, Chinchilla, southeast Queensland, Australia (Middle represent a significant north-eastern geographic extension for Pliocene); QMF52290 isolated RM2 fragment, QML1420 Pliocene koalas, and provide the first unambiguous evidence Marmor Quarry, central eastern Queensland, Australia for the presence of koalas in the assemblage. Similarly, new (Middle Pleistocene; Table 1). records of Phascolarctos from the Marmor and Mt. Etna Description. RM1, 2 or 3, description based on QMF52289: deposits extend the northern geographic distribution of Pleisto- Metacone only major cusp preserved, very large, worn; cene koalas from central eastern Australia (e.g., Price, 2008a) postmetacrista moderately developed, descends apex of to northeastern central Queensland. Thus, the new koala metacone posterobuccally to small stylar cusp E; buccal crest records are important because they show that Phascolarctos small but distinct, directed anteriorly from stylar cusp E, has been closely associated with eastern Australian habitats slightly ascending buccal margin of tooth; posterior cingulum since the Middle Pliocene. large, worn; molar enamel crenulated at posterolingual base of metacone. Palaeoecology. The modern Koala, Phascolarctos cinereus, RM2, description based on QMF52290: Protocone is mostly restricted to open forests and woodlands of eastern only major cusp preserved; preprotocrista well developed, Australia (Moore & Foley, 2000), but has been recorded, descends anterobuccally to lingual portion of anterior albeit as a rare component, in rainforest communities cingulum; postprotocrista descends posterobuccally to base (Williams et al., 1996). Koalas are folivores and feed almost of protocone; rib descends protocone between pre- and exclusively on the leaves of certain species of Eucalyptus postprotocristae, well developed; anterior fossette well (Moore & Foley, 2000). Thus, because fossil species of developed at anterior base of protocone; lingual cingulum Phascolarctos such as Ph. stirtoni, have morphologically Price et al.: koala palaeoecology 45 Fig. 4. Photographs of fossil koala teeth from eastern Australia. (A) QMF52288, LM2 of Phascolarctos sp., site QML1384, Mt. Etna. (B) QMF52289, RM1, 2 or 3 metacone fragment of Ph. ?stirtoni, Chinchilla. (C) QMF52290, RM2 protocone fragment of Ph. ?stirtoni, Marmor. similar dentitions to Ph. cinereus (Bartholomai, 1968), (Price & Sobbe, 2005). Therefore, those observations suggest the underlying assumption is that they had broadly similar that significant regional habitat changes have been underway habitat and dietary preferences (Archer et al., 1991). since at least the Middle Pliocene. The Chinchilla Local Fauna represents a rich and diverse The Middle Pleistocene Marmor (Site QML1420) assemblage of fossil taxa, many of which are considered to faunal assemblage includes dasyurids, thylacinids, be restricted solely to Pliocene deposits (e.g., Euryzygoma) possums, marsupial lions, wombats, diprotodontoids, (Archer, 1977b). The fauna includes molluscs, fish, lungfish, macropodoids, and rodents (Longman, 1925; Hocknull, crocodiles, turtles, squamates, birds, rodents, dasyurids, 2005). The palaeohabitat is interpreted as representing a bandicoots, diprotodontoids, wombats, marsupial lions, mosaic vegetation complex comprised of sclerophyll forest kangaroos, wallabies, and rodents (Bartholomai & Woods, and grasslands based on the presence of closed forest taxa 1976; Hutchinson & Mackness, 2002). The Pliocene (e.g., tree kangaroos and pademelons) and open woodland palaeohabitat of the region was interpreted as consisting of taxa (e.g., grazing kangaroos and wombats) (Hocknull, a seasonal wetland component, with grasslands interspersed 2005). The presence of Phascolarctos ?stirtoni supports an with complex and mature woodlands (Hutchinson & open woodland component of the Pleistocene habitat. The Mackness, 2002). The interpreted Pliocene habitat differs interpreted palaeohabitat differs from the modern habitat significantly from the habitats of the region today, which of the region, which is dominated by open woodlands and are dominated by open Acacia and Eucalyptus populena grasslands, with refugial forest and vine thickets restricted woodlands and grasslands (Fensham & Fairfax, 1997). to the hillsides. Although some arboreal taxa such as tree Dawson (2004) recently described the first record of a kangaroos are now locally extinct, extant Koala populations potentially arboreal tree kangaroo from the assemblage. persist in the region. Thus, the identification of Phascolarctidae gen. et sp. indet. Site QML1384 (Mt. Etna, Unit “L.U.”) contains a diverse and Phascolarctos ?stirtoni significantly increase the known faunal assemblage including squamates, turtles, dasyurids, diversity of arboreal forms within the Chinchilla Local bandicoots, possums, kangaroos, bats, and rodents. Hocknull Fauna. Although the presence of such taxa provides support (2005) suggested that the palaeohabitat was an angiosperm- for the former existence of large-scale complex woodlands, dominated rainforest based on the presence of “specialist” they do not necessarily indicate Pliocene closed-forest in the extant rainforest taxa such as cuscuses (Strigocuscus), striped region (Dawson, 2004). The modern Koala, Ph. cinereus, is possums (Dactylopsila), tree kangaroos (Dendrolagus), extant in the region, whilst tree kangaroos are now restricted and giant white-tailed rats (Uromys). The new record of to rainforest communities in northeastern Queensland and Phascolarctos sp. in the assemblage suggests the possibility New Guinea. Tree kangaroos are also absent from nearby that a more sclerophyllous open-forest habitat type was intensively-sampled Late Pleistocene deposits of the eastern also sampled in the deposit. That interpretation does not Dar ling Downs and Gore (Bartholomai, 1977; Price & Sobbe, necessarily refute the hypothesis that the palaeohabitat was 2005; Price & Webb, 2006; Price et al., 2009). Generally, predominantly rainforest, but it does suggest that Eucalyptus both the Late Pleistocene Darling Downs and Gore fossil may have formed a minor vegetative component of the faunas are dominated by terrestrial, non-arboreal, open palaeohabitat. Thus, the Middle Pleistocene vegetation wood land and grassland taxa (Bartholomai, 1977; Price, surrounding the QML1384 “L.U.” deposit may have 2002, 2005; Price & Sobbe, 2005; Price et al., 2005, 2009; consisted of a mosaic of habitat types. Such mosaic habitat Price & Webb, 2006) with very few species that also occur types appear to be characteristic of many pre-Holocene in Pliocene deposits (a possible exception being a species of Australian fossil deposits (Lundelius, 1983, 1989; Price, marsupial “tapir”, Palorchestes (Price & Hocknull, 2005)). 2005). Alternatively, the deposit represents a significantly Thus, those data suggest that significant habitat and faunal temporally-mixed assemblage. U/Th dating of the deposit reorganization occurred in the Chinchilla region between (Table 1) provides only minimum ages of deposition the Pliocene and Pleistocene, presumably reflecting the and thus, the precise duration of accumulation cannot be contraction of dense woodlands and expansion of open determined. The provenance of fossil material is unclear. It woodlands and grasslands. A local reduction in habitat is possible that different habitats occurred, and were sampled heterogeneity (associated with an expansion of open habitats) proximal to the cave over the period of deposition. However, is also evident between the Late Pleistocene and Recent this hypothesis cannot be tested on the basis of the data 46 Records of the Australian Museum (2009) Vol. 61 uncorrected corrected initial230230234238Th Age (ka) Th Age (ka) (U/ U) 333±13 332±14 1.466±0.016 267±5 267±5 1.851±0.011 153.8±1.3 153.8±1.3 3.226±0.008 152.3±5.7 147.8±10.9 2.461±0.055 122.9±0.7 122.9±0.7 1.4735±0.023 et alwing the method of Ludwig . (1992). Errors are at 2 σ-6-1 230 = 9.195×10 yr(for Th), respectively. 2 errors in λσ230g the non-radiogenic U-Th component with average upper carlcsehtaUMifcnioaaeoxunhikcnmtig vuutredavenkiarhensrin v lafennlp ertyldoeygslniartuo egtr ar eetl tmssawPel httch siyarisa(lhtt) elentt issyrH ai as emgtb of tvr udtsohfo)nooehaadcr.Gacsrfsr ioeteon . emlukiR nmatTclkavClnhaetb etelesup ue nre lbdg cocelaeicrlt oahnrlant frfSf ortna etoido.haedusnns ror rsW itvarl fdtl g sesabsohobo aiinssieaDlgreisntslus liete ty.ticifioM,inas,hs t o)eQ ryctttna tiea2n tahs acnMt.enmso0 hn neekrEcW.f0se td aLe tG.il 7 mr nMin1oMHaiAl)rank 3sem.ieis l niisg8adenadfiiT afon4txtdsdeooehlhrod lls(ylr fedeeGn ee,e a Mr , E.M sn. acgPPJl ta.odaoan.- Cllni,nWrela ecd dldmcopeisiae ds saotesaclszNottvlob kltuooekiraeebco orcc i ex r (i evsnPee((aeQotltiQQ,nn gitlrv eueneSaeaeuuicadeiocsat ,eeolsi ecn tn eegfltwfinlodouonnsoarisse,famssgrcun l llltwpieanlaaah tac hhnnnnnoaaeataydedddeessfsrl Table 1. U-series isotopic data for eastern Australian fossil localities. 232230232234238230238sample site material age U (ppm) Th (ppb) (Th/ Th) (U/ U) (Th/U) name interpretation ROK27 QML1384 calcite filling min. age 0.0822±0.0001 7.61 38.6 1.1777±0.0024 1.1795±0.0073 cal Lower Unit in bone ROK27 QML1384 macropod min. age 4.6035±0.0048 15.14 1278 1.3991±0.0027 1.3856±0.0069 bone Lower Unit bone ROK12 QML1420 tooth min. age 13.6008±0.0291 7.32 11583.8 2.4393±0.0037 2.0554±0.0085 Lower Unit ROK12 QML1420 calcite within min. age 0.0918±0.0001 33.16 13.4 1.8701±0.0053 1.5338±0.0299 Lower Unit tooth ROK13 QML1420 tooth from min. age 1.8465±0.0010 1.37 3835.6 1.3342±0.0018 0.9391±0.0029 Lower Unit breccia Note: Ratios in parentheses are activity ratios calculated from the atomic ratios, but normalized to measured values of secular-equilibrium HU-1 standard follo230-10-1238-6-1234level. Th ages are calculated using Isoplot EX 2.3 (Ludwig, 1999) with decay constants = 1.551×10 yr (for U, = 2.835×10 yr(for U) and λλ238234230238234238230the uncorrected ages were propagated directly from the uncertainties in the (Th/U) and (U/U). The corrected (corr.) Th age was calculated assumin232238230234238crustal Th/U atomic ratio of 3.8±1.9 (Th, U and U are assumed to be in secular equilibrium). Such corrections have little impact on the ages. AAAAAAAAAAMmcfDtUapSIonunraorrrrrrpnirrr iatundrsccccccccctcHelisOSSaAsMfMDQmSN(ltK7SRePttisc hdihhhhhivhahhrhernMyectsxey9tneuolaoopoeehpuu.rieeeeeeeeaeoresleuieeistmSpu–p,nrcuveeorairsmrrrrrryeooser rdra mtrrrsr,aL,,,,,met1e.,rsdnsdet,metc,l sKp ey,esce riW M hoQr aMil utdom0iM,,rod eMMMsns RtyoiuMitMaa.)B n M s.yth:apyioiu6nu nWda suP.A slmto.C raotn.Bt Wek,.iii...o flem.e pio,.. i.eAtse o,dG,,,taa.v ace u,,1 re, oai h) opeiR1, Pine dA1 .lvfconkuseaK nc o1m&1 m9ale nra &ak&9n fSatl :8eheeHe1 hQdnssnnadff9l79 rtit sCs.7sr, vs .r eteio:etomo an9 l i e S w27t7,.Jert layutSe.S8yMmBdonghM(res mMc3maets 7t.a.67l,d e,Doo .. siP u lntreei&pnb b1 Pla J7lBtt.apuu ce.ipHeKl .acWd. nP ithoa.d r–eilyta lA.Qb hTtntrasr atPci opah sierA S iioscWfa 3oroee Hea.aes’.tKkMtoPt thoareu e ue inaos lae5tnvCue lssrJioi nfanubyy rOaaksoauea nl c1ndnn c. .iml&ouitRha1 l.ftsnEen b neidsadodhc oBo os .rl ranrscswiiI0.nd t aA,dte eybee n&aoeil Anmfdu1en e ao heTKta: g(s, Rd,g, lor dZnfE chuc onn 8N r plesi(l, ru4rCiTQpt hir1a.gehc aah1Demyhdan:vc noHhoha ee9 s1r ehrai9,ieaniei9N toun ai3cnamsnaweo cnftPlrtfo–. 9.vderi8id7olhlecc sr Cr7 a nntoAnev,ersi5uW 0a 8ofia o7i caa eerG 6eKlnSK–itpt ktodeMre 9t 8(ee7laodm n.lnantsSl D.gio3upMoR dz nlloetieoR ,.n8s.olaabsdeaEi oiu uK 9at.oaRa et dado1nlcnnn eianaiM,nMR rarts2ttn.arivvlo llt y 2oaega,)hhlcisicoaedcrcia1cn0h o eeHsgnn ssasularia7 heutlre, .9oR–dWeecl oalaC uime if au ltrrb 9odouMmPandoQ(9oe hl2 l nfsssnpslZpUewaap d)pf.mcts osrntr7fseu8usd iAi ,auevassleo k,me) o1aiM odtrnui.p.Bpe m am epdfieea s s nolncu7aneiZp1gsioFiGVienat aehniecvle n.luans:aaor sapip9Qinaf doodon rr1 a entiel,lid Alealir3 trAo.9rs cctvaioig lt,srVr7doory u aton ,aa6a i)trktmnh1slsar chliT7iof Rroah(,eehlt)attolcc7t in n ot . ci oLeo. 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