OFR 151.pdf - CRC LEME
OFR 151.pdf - CRC LEME
OFR 151.pdf - CRC LEME
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Microfloras preserved in the Lower Lygistepollenites balmei Zone interval (Pebble Point Fm.)<br />
are dominated by Podocarpaceae (Podocarpus-Prumnopitys, Lagarostrobos) with lesser<br />
amounts (3-8%) of Araucariaceae (Agathis/Wollemia), Dacrydium, Microcachrys,<br />
Phyllocladus, Blechnaceae-type, Gleicheniaceae and Sphagnum. Nothofagus (Brassospora,<br />
Fuscospora) increases from ~1% to 4% up-section. Other angiosperms are uncommon except<br />
for Proteaceae (up to 8%) and Callitrichaceae (3-4%) but rare types include Casuarinaceae,<br />
Austrobuxus-type, Gambierina, and Xylomelum occidentale-type.<br />
Microfloras from the overlying Upper L. balmei Zone (Dilwyn Clay) are dominated by<br />
gymnosperms and cryptogams but are more diverse due to the increasing angiosperm<br />
component. Species first appearing in this interval include Anacolosa (Anacolosidites<br />
acutullus) and Tiliaceae (Intratriporopollenites notabilis). Nothofagus and Callitrichaceae<br />
become rare whilst Myrtaceae (M. eugeniioides) comprises up to 17% of the total pollen<br />
count. Nothofagus is uncommon in a similar Proteaceae and Myrtaceae-dominated Late<br />
Paleocene microflora in the Latrobe-1 well in the Port Campbell Embayment.<br />
Microfloras from the onshore Torquay Sub-basin to the east of Princetown include<br />
correlatives of the Lower and Upper Lygistepollenites balmei Zones (M.K. Macphail unpubl.<br />
data). The earlier zone is dominated by ancestral Nothofagus and Proteaceae spp., with<br />
frequent Araucariaceae (Araucaria, Agathis/Wollemia) but Casuarinaceae and Gambierina<br />
are rare. The younger zone is dominated by Araucariaceae (Araucaria, Agathis/Wollemia),<br />
Podocarpaceae (Podocarpus-Prumnopitys) and Gleicheniaceae, associated with Cyatheaceae,<br />
Matoniaceae, Dicksoniaceae, Dacrycarpus, Dacrydium, Halocarpus, Lagarostrobos,<br />
Anacolosa (Anacolosidites acutullus, A. sp. nov.) and an undescribed member of the Northern<br />
Hemisphere Triprojectites group (Integricorpus).<br />
Inferred climate<br />
The Lower Lygistepollenites balmei Zone assemblages represent a form of Austral Conifer<br />
Forest growing under relatively cool (lower mesotherm) and uniform to weakly seasonal and<br />
wet (humid) conditions. The expansion of angiosperms during Upper L. balmei Zone time is<br />
consistent with warming temperatures although the absence of palms indicates mean values<br />
remained within the mesotherm range.<br />
5. Gippsland Basin<br />
Paleocene sediments reach thicknesses of up to 950 m in the offshore Gippsland Basin and<br />
have been intersected in some 650 wells. A review of the well data (Macphail et al. 1994,<br />
A.D. Partridge pers. comm.) indicates that Lygistepollenites balmei Zone microfloras<br />
primarily are dominated by podocarps (Podocarpus-Prumnopitys, Lagarostrobos) and<br />
Proteaceae, with lower, but still high, relative abundances of Dacrydium (including L.<br />
balmei), ancestral Nothofagus (Nothofagidites endurus) and Callitrichaceae. Araucariaceae<br />
(predominantly Dilwynites) are most abundant in distal marine facies, due to the Neves<br />
Effect.<br />
Comparisons of Lower and Upper L. balmei Zone sequences, for example in the Tuna Field<br />
wells (I.R. Sluiter and M.K. Macphail unpubl. data), indicate that angiosperms such as<br />
Gambierina, Peninsulapollis gillii and Tetracolporites verrucosus are more common in the<br />
Early Danian than in younger (Late Danian-Early Thanetian) assemblages. The reverse is<br />
true of ancestral Nothofagus, Callitrichaceae and several extinct Proteaceae. By Late<br />
Thanetian, Gleicheniaceae, Cyatheaceae, Proteaceae and ancestral Nothofagus had replaced<br />
Lagarostrobos, Dacrydium and Callitrichaceae as the most common taxa.<br />
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