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OFR 151.pdf - CRC LEME

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5. TIME SLICE K-5<br />

Age Range: Early Campanian [83- ~70 Ma]<br />

Zones: Nothofagidites senectus Zone<br />

Upper Nelsoniella aceras to Xenikoon australis Zones<br />

5.1 Macrofloras<br />

Douglas (1994) has noted that leaf cuticle is often a major component in microfossil<br />

preparations.<br />

5.2 Microfloras<br />

Marine and non-marine sediments, which preserve Early Campanian palynofloras, occur in<br />

offshore basins along the southern, western and northern margins. The first appearance of<br />

Nothofagidites is widely used as a marker for the basal Campanian and this may conceal<br />

diachronous or time-transgressive trends in the first occurrence of other botanically important<br />

species along the southern margin.<br />

Like Lagarostrobos and Dacrydium, the first appearance of Nothofagus is of potentially<br />

major palaeoclimatic significance, as three of the four living subgenera (Fuscospora,<br />

Lophozonia, Nothofagus) are confined to relatively cool to cold (microtherm range) and<br />

uniformly wet climates in Australia, New Zealand and southern South America. The fourth<br />

subgenus (Brassospora), which is endemic to New Caledonia, New Guinea, is also confined<br />

to uniformly wet climates but is tolerant of a wider temperature range (upper microthermlower<br />

mesotherm).<br />

The clade represented by Campanian Nothofagidites was ancestral to the four extant<br />

subgenera (Dettmann et al. 1990) and its palaeo-distribution makes it probable that the genus<br />

was adapted to extended periods of winter darkness (possibly deciduous) and high levels of<br />

environmental disturbance. The latter characteristic is retained by many living Nothofagus<br />

species whilst the deciduous trait occurs in several Nothofagus species that are confined to<br />

upper subalpine and alpine habitats, e.g. N. gunnii in Tasmania.<br />

Accordingly, the spectrum of responses to modern drought and temperature extremes makes it<br />

unwise to rely too closely on modern bioclimatic data when interpreting Late Cretaceous<br />

palaeoclimates. For example, the possibility exists that ancestral Nothofagus species were (or<br />

included) shrubs occupying exposed and/or disturbed sites such as along rivers and therefore<br />

that the relative abundance of its pollen may reflect edaphic factors rather than climate per se.<br />

Conversely, there is weak evidence that some ancestral Nothofagus were growing in the<br />

Eastern Highlands, implying some ecotypes were adapted to more stable environments. An<br />

example is the high relative abundance of Nothofagidites senectus in the Wild Dog-1 well,<br />

located on the southwestern margin of the Gippsland Basin adjacent to the South Gippsland<br />

Range (Macphail 1993). Systematic analysis of Campanian microfloras across the Gippsland<br />

Basin would help resolve this point.<br />

189

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