OFR 151.pdf - CRC LEME
OFR 151.pdf - CRC LEME
OFR 151.pdf - CRC LEME
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(Morgan 1977, McMinn 1981a, Martin 1988, 1991b, 1997b, Macphail 1996c, 1997a). The<br />
age determinations are based on floristically impoverished Nothofagidites assemblages that<br />
lack index species found in younger (Late Miocene-Pliocene) or older (Eocene) microfloras.<br />
None of the zone index species used to subdivide Oligocene-Middle Miocene time in<br />
southern Australia have been recorded to date in central Australia and the age determinations<br />
remain provisional.<br />
1. Callabonna Sub-basin<br />
The one known assemblage from the Namba Formation is moderately diverse, with<br />
dominance shared between Cyathea (10%), gymnosperms (total 21%) and Restionaceae<br />
(39%). Frequent to common types are Podocarpus-Prumnopitys (9%), Dacrydium (5%),<br />
Lagarostrobos (3%), Phyllocladus (3%), Nothofagus (Brassospora) spp. (4%), Sparganiaceae<br />
(5%) and Cyperaceae (2%). Rare taxa include Araucariaceae (Agathis/Wollemia),<br />
Anacardiaceae, Caesalpinaceae and Eucalyptus. Proteaceae are absent.<br />
2. Alice Springs District<br />
Pollen dominance is shared between Gleicheniaceae, Podocarpaceae (Podocarpus-<br />
Prumnopitys), Casuarinaceae and Nothofagidites (Brassospora) spp. For example the<br />
Borehole RN 16861 is wholly dominated by Nothofagus (Brassospora) spp. (59%) with lesser<br />
amounts of Casuarinaceae (27%), Podocarpus-Prumnopitys (7%) and Dacrydium (4%). Low<br />
numbers of Botryococcus cysts imply the depositional environment was an ephemeral,<br />
brackishwater lake.<br />
Correlative Nothofagus (Brassospora) microfloras from the Burt Plain Basin occasionally<br />
include frequent to common numbers of Blechnaceae, Araucariaceae (Araucaria), Malvaceae<br />
(Malvacearumpollis) and unidentified tricolporate types. Rare taxa include Pteris,<br />
Araucariaceae (Agathis/Wollemia-type), early records of Sprengelia-type (Epacridaceae) and<br />
Grevillea-Hakea (Proteaceae), Menyanthaceae (cf. Villarsia), Onagraceae (cf. Epilobium) and<br />
an unidentified Sparganiaceae. Cyperaceae, Myrtaceae (including Eucalyptus) and<br />
Restionaceae are very rare or absent.<br />
Assuming that the Namba and Alice Springs sequences are broadly contemporary, relative<br />
abundances appear to have been shaped by the depositional environment and regional<br />
topography. For example, the prominence of Nothofagus (Brassospora) spp. in the Alice<br />
Springs district compared to the Lake Eyre Basin almost certainly is due to the proximity of<br />
uplands such as the McDonnell Ranges. Conversely sedges and other swamp taxa are better<br />
represented in the low-lying Lake Eyre Basin. Apart from Casuarinaceae, which may include<br />
the dry sclerophyll genera Allocasuarina/Casuarina as well as Gymnostoma, it is unclear<br />
which taxa occupied dry interfluve sites. Halophyte taxa such as Chenopodiaceae-<br />
Amaranthaceae (Chenopodipollis chenopodiaceoides) or Wilsonia (Tricolpites trioblatus)<br />
appear to be absent although both occur in saline-influenced deposits in the Murray Basin by<br />
this time.<br />
Inferred climate<br />
The floristically and ecologically heterogeneous composition of the microfloras in central<br />
Australia point to relatively cool (lower mesotherm) and seasonally wet (humid) conditions in<br />
which mean summer rainfall was inadequate to support rainforest trees away from stream<br />
banks or sheltered gullies. The ephemeral nature of depositional environments also point to<br />
dry summers during which rivers fragmented into brackishwater swamps.<br />
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