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OFR 151.pdf - CRC LEME

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3.2 Microfloras<br />

Many of the macrofossil deposits preserve diverse microfloras, leading to parallel, albeit often<br />

different palaeoclimatic interpretations. Regions for which only microfossil data are available<br />

are the Bight region (Eucla Basin) and Alice Springs district (Ayers Rock, Hale, Huckitta,<br />

Santa Teresa, Ti-tree Basins) (Milne 1988, Macphail 1996c, 1997a, Clarke 2000).<br />

Of particular importance are Middle (Lower N. asperus Zone) and Late (Middle N. asperus<br />

Zone) Eocene sequences preserved in the offshore Gippsland and Bass Basins. Reasons<br />

include the high exposure of the basins to events occurring in the Southern Ocean, the<br />

unequalled density of drilling and sampling (up to 120 conventional and sidewall core<br />

samples per well) and concomitant highly detailed lithostratigraphic and geophysical database<br />

(cf. Glenie 1986, Macphail et al. 1994). Unlike basins in central, western and northern<br />

Australia, sufficient assemblages have been analysed over the past three decades to be certain<br />

that a number of fossil species found in central Australia and the Murray Basin during the<br />

Middle-Late Eocene had not migrated as far south as the Gippsland and Bass Basins.<br />

Elsewhere, much potentially fossiliferous material recovered in western New South Wales,<br />

Victoria and South Australia in the 1970s-1980s, was discarded before being pollen-analysed.<br />

Nevertheless the existing microfossil database for the Murray-Darling Basin is second only to<br />

the Gippsland Basin in terms of sample numbers. The basin covers a greater geographic area<br />

(~300,000 km 2 ) than any other Cenozoic basin in Australia (Macphail 1999). Foraminiferal<br />

data provide independent age control in the south-west of the basin (Lablack 1991) but some<br />

age determinations and species time distributions may have compromised by the nature of the<br />

material (cuttings) made available for analysis. Detailed reviews of the microfloras have been<br />

published for the western (Truswell et al. 1985, Martin 1991a), central (Macphail and<br />

Truswell 1989, 1993, Macphail 1999) and eastern (Martin 1973, 1987, 1993) sectors of the<br />

Murray Basin. Martin (1993) has summarized changes in the relative proportion of major<br />

vegetation types within five sectors of the basin via pollen groups averaged for each<br />

palynological zone.<br />

A feature common to all microfloral assemblages from southern and central Australia, is the<br />

high relative abundance and diversity of Nothofagus (Brassospora) spp., especially<br />

Nothofagidites emarcidus-heterus. Nevertheless floristic differences point to significant<br />

bioclimatic gradients between the north/west and south/east regions of the continent. For<br />

example, megathermal taxa such as Nypa are confined to northern Australia and the eastern<br />

Eucla Basin whilst Nothofagus (Lophozonia) spp. are frequent only in eastern Australia and<br />

Tasmania but are rare or absent in southwestern and northwestern Australia (Stover and<br />

Partridge 1982).<br />

3.2.1 North-West Australia<br />

Middle-Late Eocene microfloras are preserved in some bioclastic carbonate facies in the<br />

Bonaparte Basin (Cobia-1, Jacaranda-1). These are dominated by dinoflagellates, and the<br />

minor spore and pollen component almost certainly represents the more prolific pollen and<br />

spore producers in the riparian and regional dryland vegetation. Because of poor<br />

preservation, processing may have concentrated downhole contaminants. Age determinations<br />

are mostly based on marine microfossils.<br />

1. Bonaparte Basin<br />

Yields from Cobia-1 (365-380 m) are inadequate to determine relative abundance but the<br />

most frequently recorded taxa are Casuarinaceae (Gymnostoma) and unidentified tricolporate<br />

230

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