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OFR 151.pdf - CRC LEME

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Dacrydium and its extinct relation Lygistepollenites balmei) and Ephedra. Uncommon to rare<br />

angiosperms include: Anacolosa (Anacolosidites cf. A. acutullus), Beauprea (Beaupreaidites<br />

elegansiformis, B. verrucosus), Callitrichaceae, Chloranthaceae (Clavatipollenites hughesii),<br />

Ericaceae-Epacridaceae, Gambierina, Integricorpus, Liliaceae, Trimeniaceae<br />

(Periporopollenites demarcatus), tricolporates including Neoscortechinia-type (Tricolporites<br />

lilliei, Tricolporites cf. T. lilliei), and Winteraceae (Pseudowinterapollis). Four probable<br />

palm genera are present (Arecipites, Longapertites, Nupharipollis, Spinizonocolpites).<br />

Inferred climate<br />

These assemblages are difficult to interpret ecologically since palms, which imply very warm<br />

to hot, upper mesotherm temperatures, were growing in the Ayers Rock Basin, at<br />

approximately the same time as Sphagnum bog, which imply microtherm range conditions<br />

surrounded the Huckitta Basin. The most likely explanation is that microclimates in the two<br />

basins were different. For example the Ayers Rock microflora includes a dinoflagellate that<br />

is usually found in marine sediments (Ceratopsis obliquipes) and discharge of warm saline<br />

groundwater may explain the presence of a possible mangrove palm (Spinizonocolpites), even<br />

if mean air temperatures were cool (lower mesotherm). The presence of podocarp-dominated<br />

Austral Conifer Forest is evidence regional climates were seasonally humid-perhumid in both<br />

basins.<br />

6.2.4 South-West Australia<br />

1. Carnarvon Basin<br />

Microfloras preserved in marine sediments in Alpha North-1 provide a record of the Late<br />

Campanian to Maastrichtian plant communities growing on the margins of the Carnarvon<br />

Basin (M.K. Macphail unpubl. results). Fossil spores and pollen are uncommon relative to<br />

dinoflagellates but the sequence has the advantage that the individual microfloras have been<br />

precisely dated using nannofossils (Rexilius 1989).<br />

Samples yielding statistically significant (>150) numbers of miospores range in age from the<br />

latest Late Campanian to basal Middle Maastrichtian. Dominant taxa are Proteaceae and<br />

cryptogams. The angiosperm component lacks many of the distinctively ornamented<br />

Proteacidites spp. found in the northern and southern margin basins and, apart from<br />

Proteaceae, only unidentified tricolpate and tricolporate types occur in above-trace numbers.<br />

Rare taxa include Beauprea, Chloranthaceae (Clavatipollenites hughesii, C. sp. cf. C.<br />

glarius), Gambierina, Ilex and Liliaceae. Uncommon to rare cryptograms include Lophosoria,<br />

Anemia and Lycopodiaceae. Palms and temperate rainforest taxa such as Nothofagus are<br />

absent. The only frequent to common gymnosperms are podocarps (Podocarpus-<br />

Prumnopitys, Podosporites microsaccatus) and possible pteridosperms (Alisporites).<br />

Uncommon to rare gymnosperms include cheirolepidiacean conifers, Ephedra, podocarps<br />

(Dacrydium including Lygistepollenites balmei, Lagarostrobos, Microcachrys) and<br />

araucarians (chiefly Agathis/Wollemia). Common cryptogams include Cyatheaceae,<br />

Gleicheniaceae (Clavifera, Gleicheniidites) and Sphagnum.<br />

The palaeovegetation appear to have been a floristically impoverished variant of the fern<br />

heath and Austral Conifer Forest communities recorded further to the north in the Browse and<br />

Bonaparte Basins.<br />

196

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