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OFR 151.pdf - CRC LEME

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producing cicatrose to canaliculate trilete spores (Cicatricosisporites, Contignisporites,<br />

Ruffordiaspora) had a cosmopolitan distribution that extended into very high latitudes whilst<br />

their NLRs (Anemia, Mohria, Ruffordia) are confined to tropical America, Africa and<br />

southern India (Dettmann and Clifford 1991, 1992). The same is true for the Araucariaceae,<br />

which are mostly confined to seasonally wet and warm to hot (mesotherm-megatherm)<br />

climates. Nevertheless, most of the plants that first appear during the Early Cretaceous<br />

survived into latest Cretaceous or early Palaeogene time. Consequently presence/absence<br />

data give the misleading impression that the Early Cretaceous vegetation was homogeneous<br />

across the continent.<br />

Contributing to this impression of apparent uniformity is the mixing of palynofloras within<br />

the larger basins, most of which received water-transported miospores via rivers draining vast<br />

tracts of the continent. Examples are the Canning-Officer and Carpentaria-Eromanga<br />

Seaways and the Australo-Antarctic Rift System. In contrast, microfloras derived from coals<br />

or lignites mostly represent local mire communities. Climatically-forced provincialism of the<br />

flora had developed as early as the Valanginian [135 Ma]. For example, one clade of<br />

brachyphyll araucarians (Balmeiopsis) is restricted to the drier, palaeo-northern side of the<br />

continent (present-day northwestern to southwestern Australia) whilst the liverwort<br />

(Foraminisporis wonthaggiensis) was restricted to the wetter, palaeo-southern side of the<br />

continent (present-day northeastern to southeastern Australia).<br />

Pollen data from northern and central Australia show that the primitive angiosperms<br />

(angiospermids sensu Vasanthy et al. 1990) expanded over the continent during the mid<br />

Cretaceous. Examples in the Eromanga Basin (times of first appearance in parentheses) are:<br />

Clavatipollenites hughesii (Barremian/Early Aptian), Asteropollis asteroides (basal Albian),<br />

Phimopollenites and Tricolpites (mid Albian) and tricolporate pollen types (Late Albian).<br />

Angiospermid pollen first occur in significant numbers in the Surat Basin at the<br />

Aptian/Albian boundary and show a marked increase in relative abundance during the Albian.<br />

Since the highest relative abundance values follow regressive movements of the<br />

palaeoshoreline, the earliest angiosperm communities are likely to have been riparian and/or<br />

colonisers of newly exposed seafloor sediments.<br />

5.3.2 Gymnosperms and cryptogams<br />

Mesozoic forests and woodlands growing at polar latitudes in Australia were dominated by<br />

gymnosperms and cryptogams. This woody biome has no living counterpart in the Southern<br />

Hemisphere but a general resemblance to the boreal conifer forests and taiga of the Northern<br />

Hemisphere is likely for bioclimatic and ecophysiological reasons. The name Austral Conifer<br />

Forest is coined here to emphasise the presumed eco-physiognomic relationship. Some<br />

Cretaceous plants were deciduous, e.g. the pteridosperm/pentoxylalean genus Taeniopteris,<br />

but it is unlikely that the deciduous habit per se was advantageous at polar latitudes in the<br />

Southern Hemisphere (cf. Wolfe 1987, Hill et al. 1999). Empirical evidence for this includes<br />

the prominence of evergreen gymnosperms in coastal palaeo-southern Australia and their<br />

relative rarity in coastal palaeo-northern Australia during the Late Cretaceous.<br />

Creber and Chaloner (1985) note that the amount of light energy available at polar latitudes<br />

during summer months is not dissimilar to that received annually in the middle latitudes.<br />

Hence the light available within polar communities of widely spaced trees with tall conical<br />

crowns may not have been substantially less than light availability within more dense plant<br />

communities growing at lower latitudes. Similarly, a study of the response of selected<br />

Southern Hemisphere tree species to prolonged darkness (Read and Francis 1992) suggests<br />

that survival rates are higher under colder (>4 0 C) than under warmer temperature regimes.<br />

Some species were able to survive 10 weeks of continuous darkness and Bond et al. (1999)<br />

have shown that the foliage of one Northern Hemisphere pine (Tsuga) can survive under less<br />

than 1% of full sun light in humid temperate climates.<br />

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