OFR 151.pdf - CRC LEME
OFR 151.pdf - CRC LEME
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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