2006
DOI: 10.1080/03115510608619570
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Current status of species-level representation in faunas from selected fossil localities in the Riversleigh World Heritage Area, northwestern Queensland

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Cited by 18 publications
(39 citation statements)
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“…In addition, our demonstration of profound antiquity for modern desert-living bandicoot lineages (a result unaffected by alternative constraint parameters or variation in substitution rate16: Supplementary Tables S6–S8; Supplementary Figs S21–S30), indicates that increasing aridity during the late Neogene likely did not initiate the genesis of crown Perameloidea, although it probably assisted in perameline intra-clade habitat expansion and localized speciation events. The undeniable rarity of definitive crown perameloid fossils in pre-Pliocene sediments might therefore be explained by sampling biases and/or incompletely documented collections3275859, as well as ecological underrepresentation60. Indeed, our tree-based ancestral area optimisations (Supplementary Tables S9–S12; Supplementary Figs S31–S34) infer that the seminal radiation of modern bandicoots accompanied widespread australidelphian niche dispersals into drier mosaic settings, perhaps such as mallee ( Eucalyptus ) woodlands that spread through Central Australia from the late Oligocene5061.…”
Section: Discussionmentioning
confidence: 99%
“…In addition, our demonstration of profound antiquity for modern desert-living bandicoot lineages (a result unaffected by alternative constraint parameters or variation in substitution rate16: Supplementary Tables S6–S8; Supplementary Figs S21–S30), indicates that increasing aridity during the late Neogene likely did not initiate the genesis of crown Perameloidea, although it probably assisted in perameline intra-clade habitat expansion and localized speciation events. The undeniable rarity of definitive crown perameloid fossils in pre-Pliocene sediments might therefore be explained by sampling biases and/or incompletely documented collections3275859, as well as ecological underrepresentation60. Indeed, our tree-based ancestral area optimisations (Supplementary Tables S9–S12; Supplementary Figs S31–S34) infer that the seminal radiation of modern bandicoots accompanied widespread australidelphian niche dispersals into drier mosaic settings, perhaps such as mallee ( Eucalyptus ) woodlands that spread through Central Australia from the late Oligocene5061.…”
Section: Discussionmentioning
confidence: 99%
“…from the Czech Republic [122,123]; (CN10) Physignathus – Ctenophorus , 16 Mya, based on material referable to Physignathus sp. from Australia [124-126]; (CN11) Gambelia – Anolis , 48 Mya, based on Afairiguana avius the oldest pleurodontan iguanian [117,118,127,128]; and (CN12) Shinisaurus – Elgaria , 128 Mya, based on Dalinghosaurus longidigitus which may be more closely related to Shinisaurus than to any other living squamate [114,129,130]. For the full justification of each of the fossil specimens and their age see Additional file 1.…”
Section: Methodsmentioning
confidence: 99%
“…For example, molar dimensions of Neohelos tirarensis from the Kutjamarpu LF consistently group with those of N. tirarensis from Riversleigh's FZB (Black et al 2013a). In addition, a number of other Faunal Zone B taxa also occur in the Kutjamarpu LF including the casuariid Emuarius gidju, the phascolarctid Litokoala kutjamarpensis, the vombatid Rhizophascolonus crowcrofti, the thylacoleonid Wakaleo oldfieldi, the ektopodontid Ektopodon serratus, the pseudocheirid possums Paljara tirarensae, Marlu kutjamarpensis, M. ampelos, and M. syke, and the potoroid Wakiewakie lawsoni (Godthelp et al 1989;Archer et al 2006;Gillespie 2007;Louys et al 2007;Roberts et al 2008Roberts et al , 2009Travouillon et al 2011;Black et al 2013b). Specimens of M. variae from the Kutjamarpu LF are closer in size to those from Riversleigh's FZB, supporting an early Miocene in age for this central Australian assemblage.…”
Section: Biostratigraphy and Palaeoenvironment Of Species Of Madjumentioning
confidence: 98%
“…However, until now no cases of sexual dimorphism have been reported from the fossil record. Here we suggest that the two taxa noted by Archer et al (2006) and Travouillon et al (2006Travouillon et al ( , 2009Travouillon et al ( , 2011) represent a single dimorphic species, for the following reasons.…”
Section: Sexual Dimorphism In Madju Variaementioning
confidence: 98%