OFR 151.pdf - CRC LEME
OFR 151.pdf - CRC LEME
OFR 151.pdf - CRC LEME
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
Similarly it is difficult to summarise bioclimates within most of the selected geographic<br />
regions due to strengthening temperature and rainfall gradients between coastal, inland and<br />
upland districts. Nonetheless changes in miospore dominance and the palaeodistribution of<br />
some cryptogams provide unequivocal evidence of the impact of cooling followed by<br />
temporary warming during the Oligocene-Early Miocene. Examples include the marked<br />
impoverishment of Nothofagus forest in the onshore Gippsland Basin during the Eocene-<br />
Oligocene transition (Upper Nothofagidites asperus Zone) and the re-establishment of<br />
Lophosoria in southeastern Australia during the Early Oligocene (Macphail et al. 1994).<br />
Fossil spores of Lophosoria (Cyatheacidites annulatus) indicate this large ground fern, which<br />
is now restricted to cool-cold climates in South America, reached Tasmania via trans-oceanic<br />
dispersal during or slightly before the Lemonthyme Glaciation (Macphail and Hill 1994). The<br />
fern then spread rapidly northwards throughout southeastern Australia during the Early<br />
Oligocene (Proteacidites tuberculatus Zone time) but is not recorded in southern Queensland<br />
until the Early Miocene (Dettmann, 1986b), due to relatively warm conditions at lower<br />
latitudes. Increasingly dry, seasonal climates explain the failure of Lophosoria to extend into<br />
central and north-west Australia.<br />
Palaeo-northern Australia<br />
Sparse pollen evidence from the Argo abyssal plain off Port Hedland hints that continental<br />
climates in north-west Western Australia were strongly seasonal (upper mesothermmegatherm,<br />
semiarid-subhumid) although Oligocene to Early Miocene microclimates in the<br />
Pilbara region were sufficiently humid during summer months to allow Nothofagus<br />
(Brassospora) spp. and podocarps to survive along palaeochannels on the Hamersley Ranges<br />
(M.K. Macphail unpubl. data). Conditions in inland northeastern Australia appear to have<br />
been warm to hot (upper mesotherm) and seasonally very wet (perhumid) based on faunal<br />
remains and leaf impressions of subtropical-tropical rainforest species preserved in karst<br />
terrain at Riversleigh, northwestern Queensland (R.S. Hill pers. comm.).<br />
Isotopic evidence from the Coral Sea indicates SSTs in the region increased from between<br />
9.5-13.0 0 C (microtherm range) in the earliest Early Oligocene to 14.5-19.5 0 C (mesotherm<br />
range) in the Early Oligocene and reached a maximum of 20.5 0 C (upper mesotherm) in the<br />
Middle Miocene (Feary et al. 1991). Floristically complex Nothofagus communities<br />
remained the dominant vegetation type on the western slopes of the Leichhardt Range inland<br />
of Mackay, into Early-Middle Miocene (Canthiumidites bellus Zone Equivalent) time<br />
(Beeston 1994). This rainforest included taxa with cool temperate NLRs, e.g. Dacrydium,<br />
Lagarostrobos, Microcachrys and Nothofagus (Lophozonia), as well as taxa with warm<br />
temperate to subtropical-tropical NLRs, e.g. Anacolosa, Archidendron-type, Cupanieae and<br />
Ilex. How representative this flora and vegetation were of areas to the west in central<br />
Queensland is unclear. Further to the south, uniformly wet and relatively cool (lower<br />
mesotherm) climates allowed Nothofagus (Brassospora) spp. to become prominent during the<br />
Late Oligocene in coastal southern Queensland. Conditions became increasingly warm<br />
(upper mesotherm) and/or seasonally dry, resulting in the replacement of Nothofagus<br />
communities by other rainforest types during the Early to Middle Miocene. The presence of<br />
Nypa in Foram Zones N5-N7 marine sediments but not in Foram Zones N8-N9 marine<br />
sediments in the Capricorn Basin implies maximum warmth in southern Queensland occurred<br />
during the Early Miocene.<br />
The combined data demonstrate that precipitation gradients across northern Australia were<br />
parallel in direction but not as strong as those of the present-day. Because warm water flow<br />
through the Indonesian archipelago was not severely constricted until the Early Pliocene<br />
(Srinivasan and Sinha 1998), it is premature to explain these gradients in terms of modern<br />
ocean current patterns or monsoonal climates associated with uplift of the Tibetan Plateau (cf.<br />
Ramstein et al. 1997).<br />
101