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OFR 151.pdf - CRC LEME

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several taxa, which first appear in the Middle N. asperus Zone in the Gippsland Basin, are<br />

recorded in early Eocene (Malvacipollis diversus Zone Equivalent) and Middle Eocene<br />

(Lower N. asperus Zone Equivalent) microfloras in basins in south-west and central Australia,<br />

e.g. Anacolosidites luteoides and Tricolpites thomasii.<br />

In general terms, angiosperms are more prevalent than gymnosperms (av. 60-75% versus 15-<br />

30%) throughout the Middle-Late Eocene, with the most common types being Nothofagus<br />

(Brassospora) spp. and Podocarpaceae (Dacrydium, Lagarostrobos, Podocarpus-<br />

Prumnopitys), respectively. Values of Nothofagus (Brassospora) increase from ~25% in the<br />

early Middle Eocene to >50% in the late Late Eocene whilst Casuarinaceae and Proteaceae<br />

decline from ~20% to less than 1-10% over the same interval (Partridge 1999). Coal<br />

microfloras are often dominated by Lagarostrobos whilst Araucariaceae (Araucaria,<br />

Agathis/Wollemia) tend to be more abundant in marine facies (Neves Effect). Proteacidites<br />

asperopolus is often common in Lower N. asperus Zone assemblages whilst high values of P.<br />

pachypolus are confined to the Middle N. asperus Zone.<br />

Unlike other Australian basins, the Gippsland Basin database is sufficiently comprehensive to<br />

use both quantitative data and the first and last appearances of rare taxa as reliable proxy<br />

evidence for bioclimatic change within the Middle-Late Eocene. For example geological and<br />

sequence stratigraphic evidence support palynostratigraphic evidence that Nothofagus<br />

(Brassospora) spp., including one newly evolved canopy species (Nothofagidites falcatus),<br />

expanded very rapidly across the basin during the early Middle Eocene. Late Eocene<br />

rainforest appears to have been more diverse than Middle Eocene rainforest, due to the<br />

immigration of herbaceous and woody taxa, e.g. Sparganiaceae (Aglaoreidia qualumis),<br />

Anacolosa (Anacolosidites sectus), Loranthaceae (Tricolpites thomasii) and a range of extinct<br />

and extant Proteaceae. The latter includes Isopogon (Proteacidites truncatus); the former<br />

include Proteacidites confragosus, P. reticulatus and Triorites magnificus. The same<br />

diversification is reflected in the greater proportion of pollen taxa with complex<br />

ornamentation.<br />

Inferred Climate<br />

Conditions in the Gippsland Basin cooled markedly (to lower mesotherm values) during the<br />

Early-Middle Eocene transition although conditions remained wet to very wet (perhumid).<br />

Temporary warming, indicated by the appearance of Triorites magnificus during the Late<br />

Eocene, may correlate with transient warming of sea surface temperatures recorded elsewhere<br />

along the southern margin (B. McGowran pers. comm.).<br />

3.2.7 Tasmania<br />

Middle-Late Eocene facies (upper Eastern View Group) are intersected in the majority of<br />

wells drilled in the Bass Basin and onshore sub-basins in northern Tasmania but few data are<br />

available in well completion reports. It is unclear whether the plants producing Middle N.<br />

asperus Zone index species e.g. Anacolosidites sectus, Tricolpites thomasii and Triorites<br />

magnificus ever extended southwards into northeastern, central or southeastern Tasmania.<br />

1. Bass Basin<br />

Morgan (1986b) indicates Lower and Middle Nothofagidites asperus Zone Equivalent<br />

microfloras are dominated by Nothofagus (Brassospora) with lesser amounts of<br />

Casuarinaceae. The same dominance is observed in Squid-1, where two extinct Proteaceae<br />

(Proteacidites asperopolus, P. leightonii) are abundant in Lower Nothofagidites asperus Zone<br />

Equivalent (Martin 1985).<br />

2. South-east Tasmania<br />

241

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