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OFR 151.pdf - CRC LEME

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and, for Tertiary continental sequences, by the lack of a ‘local’ pollen-spore based<br />

palynostratigraphy. For example in Queensland, Sajjadi and Playford’s important (2002a,<br />

2002b) reviews of Early Cretaceous microfloras in the Eromanga Basin cites numerous<br />

species described by J. McKellar (Geological Survey of Queensland in press) in an as yet<br />

(2006) unpublished analysis of correlative microfloras in the Surat Basin. Areas for which<br />

some additional palaeobotanical evidence have been published are (1) the Bundaberg Trough<br />

in coastal southeastern Queensland (Dettmann and Clifford 2003) and The St. George Basin<br />

(Lower Balonne district) in inland southeastern Queensland (Macphail 2004b). At the former<br />

site, an Early Miocene assemblage includes what appears to be the first record of the late<br />

Early to early Late Miocene zone index species Canthiumidites bellus in Queensland. Like its<br />

probable correlative at Mt. Coolon in central Queensland (Beeston 1994), the microflora is<br />

dominated by Nothofagus (Brassospora) spp., Casuarinaceae, Euphorbiaceae and Myrtaceae<br />

but also includes rare taxa whose Nearest Living Relatives (NLRs) occur in cool temperate<br />

rainforest as well as taxa whose NLRs occur in subtropical ‘dry’ rainforest. The probable<br />

Pliocene sequences in the St. George Basin indicates climates were too dry to support<br />

temperate rainforest angiosperms such as Nothofagus although temperate rainforest<br />

gymnosperms survived along rivers and/or the adjacent uplands.<br />

Central Australia<br />

A recently recognised glacial diamicton confirms glaciers had developed some time during<br />

the Berriasian to Valanginian in the Eromanga Basin (Alley and Frakes 2003). A recent PhD<br />

study uses changes in Barremian to Aptian dinoflagellate populations to infer mid Cretaceous<br />

palaeoclimates (Oosting 2004, Oosting et al. 2006). Otherwise, there have been few additions<br />

to the palaeobotanical database although Late Eocene macrofloras at Nelly Creek in northern<br />

South Australia continue to be a focus for macrofossil research (Hill and Cristophel 2001,<br />

Conran et al. 2003). Palaeontological studies have added to knowledge of Oligo-Miocene<br />

climates, e.g. Megirian et al. (2004), but the resolution provided by the land mammal<br />

biostratigraphy remains poor. Age control based on lithostratigraphy may or may not be<br />

reliable. For example, an organic interval within the Late Oligocene Etadunna Formation at<br />

Lake Palankarinna in northern South Australia yielded an Early Eocene microflora (M.K.<br />

Macphail unpubl. data). A possible Tertiary organic sequence intersected in a recent<br />

Northern Territory Geological Survey drillhole was discarded, despite being ear-marked for<br />

palynostratigraphic dating.<br />

South-West Australia<br />

Recent additions to the palaeobotanical database include detailed analyses of (1) Late<br />

Jurassic-Early Cretaceous sequences in the offshore Vlaming Sub-basin of the Perth Basin<br />

(Backhouse 2006, Macphail 2006c), (2) Late Jurassic-Cretaceous dredge samples from the<br />

offshore Bremer and Denmark Sub-basins in the western Bight Basin (Macphail and Monteil<br />

2004, Exon et al. 2005), (3) Late Eocene lignites preserved in palaeochannels in southern<br />

south-west Western Australia (de Broekert 2003, Itzstein-Davey 2004, M.K. Macphail<br />

unpubl. data), (4) Early Oligocene to possibly Early Miocene carbonaceous clays underlying a<br />

highly important channel iron deposit (CID) at Yandi in the Pilbara region, northern southwest<br />

Western Australia (Macphail and Stone 2004), and (5) mid Pliocene lake sediments<br />

infilling a probable Early Cretaceous meteor impact crater at Yallalie, north of Perth (Atahan<br />

et al. 2004, Dodson and Macphail 2004).<br />

The offshore data provide a detailed record of Austral Conifer Forest communities before and<br />

during the onset of rifting between Australia and Antarctica, and confirm (climate-forced)<br />

provincialism of the araucarian and cryptogam floras had developed as early as the<br />

Valanginian to Early Barremian. Microfloras preserved at Yandi demonstrate that climates at<br />

higher elevations on the Hamersley Ranges were cooler (mesotherm range) and wetter (humid<br />

4

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