OFR 151.pdf - CRC LEME
OFR 151.pdf - CRC LEME OFR 151.pdf - CRC LEME
northern New South Wales. The assemblage is dominated by monolete and trilete ferns and fern allies, associated with infrequent Casuarinaceae, Euphorbiaceae, Nothofagus and (one specimen) Tiliaceae. Inferred climate The source vegetation appears to have been fern-dominated wet scrub growing under uniformly wet (perhumid) and probably cool (lower mesotherm) conditions. Whether the cryptogam dominance reflects a recent wildfire (fire succession) or highly fertile soils (edaphic disclimax) is unknown. 2.2.3 Central Australia Tertiary basins in the Alice Springs district and Lake Eyre Basin (Eyre Formation) preserve thin carbonaceous units of probable Early Eocene age (age range latest Paleocene-late Early Eocene). Many of these preserve very diverse microfloras, some of which also include dinoflagellate species that are usually associated with saline conditions (Sluiter 1991, Macphail 1996c, 1997a, Alley 1998). The reason for this is unclear but salinity levels may have been raised due to discharge of saline groundwater, leaching of salt from outcrops of Early Cretaceous or older marine sediments, e.g. the Bitter Springs Formation, or deposition within hydrologically-closed basins. Microfloras from the Eyre Formation are similar to those recorded in the Late Paleocene and, apart from the absence of mangroves, are also similar to Early Eocene assemblages found in coastal northwestern Australia. 1. Alice Springs district Early Eocene microfloras from the Santa Teresa and Ti-tree Basins, Alice Springs district are dominated by Casuarinaceae, Proteaceae including large (mostly described) and many small (undescribed) types, and tricolporate types. These are associated with occasional high values of monolete spores, Acrostichum-type (Cyathidites splendens), Gleicheniaceae and other trilete fern spores, and Euphorbiaceae (Malvacipollis). Araucariaceae, Dacrydium, Lagarostrobos (Phyllocladidites reticulosaccatus), Cupanieae and a member of the otherwise wholly Northern Hemisphere Triprojectites group (Integricorpus) are frequent in some samples. Rare taxa include Pteris, Lygodium, Lagarostrobos, Palmae (Arecipites, Longapertites, Nupharipollis), Anacardiaceae (Striacolporites cf. cephalus), Anacolosa (Anacolosidites acutullus), Beauprea, Callitrichaceae, Gunnera, Ilex, Sapotaceae (Sapotaceoidaepollenites latizonatus) and Tiliaceae. Nothofagus is very rare and the records may be due to downhole contamination. 2. Lake Eyre Basin Microfloras dated as Paleocene in Lake Eyre Bore 8A drillhole (Alley 1983a) are more likely to be Early Eocene, based on Myrtaceidites tenuis and Proteacidites pachypolus, which first occur in the Gippsland Basin in the Lower Malvacipollis diversus Zone. The assemblages are dominated by small angiosperm pollen types (possibly Cunoniaceae, Elaeocarpaceae) associated with Gleicheniaceae, Cupressaceae, Podocarpaceae (Dacrydium, Lagarostrobos, Microcachrys, Podocarpus-Prumnopitys), Ascarina, Casuarinaceae, Euphorbiaceae, Myrtaceae, Nothofagus (Nothofagidites flemingii), and diverse Proteaceae. Pollen data from the Muloorina-2 and Poonarunna-1 wells (Sluiter 1991) hint that Myrtaceae, Proteaceae, a wholly extinct lineage of Lagarostrobos (Phyllocladidites reticulosaccatus) and Podocarpus-Prumnopitys expanded at the expense of Cunoniaceae, Cupressaceae- 217
Taxodiaceae and Araucariaceae during the Early Eocene. Cyatheaceae are rare relative to the underlying Late Paleocene microfloras. Inferred climate The high degree of variation between assemblages points to the source being a mosaic of ecologically disparate taxa whose affinities may lie anywhere from modern tropical (megatherm) to cool-cold temperate (microtherm) rainforest. The combined evidence, however, implies that conditions were very warm (upper mesotherm) and seasonally very wet (perhumid). Sluiter (1991) has interpreted ecological trends in the Lake Eyre Basin as indicating the complex angiosperm rainforest types evolved in response to an increase in the mean annual rainfall and temperature (to ~22 0 C). 2.2.4 South-West Australia 1. Carnarvon Basin Basal Early to basal Middle Eocene sediments at 1135-1257 m in Alpha North-1 preserve diverse microfloras, which are dominated by Casuarinaceae (Haloragacidites harrisii), and unidentified tricolporate types and include frequent to common Euphorbiaceae (Malvacipollis diversus) and Proteaceae (M.K. Macphail unpubl. data). The gymnosperm flora is more diverse than in Jacaranda-1 (Bonaparte Basin). Gymnosperms (Araucaria, Cupressaceae, Dacrydium, Podocarpus-Prumnopitys, Agathis/Wollemia) are much more common and Myrtaceae, Cupanieae, Nypa and Restionaceae (Milfordia homeopunctata) less common than in the Bonaparte Basin. Rare taxa include Lycopodiaceae, Selaginella, Acrostichum-type (Cyathidites splendens), Gleicheniaceae, Lygodium, Pteris, Sphagnum, Anacardiaceae (Ailanthipites, Striacolporites cf. cephalus) Anacolosa (Anacolosidites acutullus), Banksia (Banksieaeidites elongatus), Convolvulaceae (Perfotricolpites), a possible Eucalyptus (Myrtaceidites tenuis), Euphorbiaceae (Malvacipollis spp.), Gunnera, Ilex, Musgraveinae (Banksieaeidites arcuatus), Nothofagus (Brassospora, Fuscospora), Nypa, Poaceae, Polygalaceae (Polycolporopollenites esobalteus), Santalum (Santalumidites cainozoicus) and Stylidiaceae (Tricolpites stylidioides). Inferred climate The paucity of megatherm taxa such as Nypa, the relatively prominent representation of gymnosperms and cryptogams, and the presence of Nothofagus indicates that mean air temperatures within the Carnarvon Basin were slightly cooler (upper mesotherm) than in the Bonaparte Basin (possibly megatherm). Rainfall may have been similar, i.e. very wet (perhumid), with a (pronounced) dry season. The apparent poor development of coastal swamps may be due to local tidal regimes rather than the regional rainfall. 2. Perth Basin Abundant angiosperm pollen, including Proteaceae, is reported to occur in dinoflagellatedominated assemblages from the Kings Park Shale interval intersected in the Sir James Mitchell Park-2A bore, Perth (Backhouse 1981). The age of this microflora is uncertain (possible Early Eocene) but Churchill (1973) and Jarzen and Pocknall (1993) have reported Nypa and Strasburgeriaceae (Bluffopollis scabratus) pollen, respectively, from the same formation. Inferred climate Assuming that the record of Nypa is correct, then conditions within the southern Perth Basin (palaeolatitude ~60 0 S) were very warm to hot (upper mesotherm) and seasonally very wet (perhumid). 218
- Page 168 and 169: APPENDIX 1 CRETACEOUS DATA 167
- Page 170 and 171: 1. TIME SLICE K-1 Age Range: Berria
- Page 172 and 173: Australian assemblages, located on
- Page 174 and 175: 2. Officer Basin Dinoflagellates in
- Page 176 and 177: 2. TIME SLICE K-2 Age Range: Aptian
- Page 178 and 179: Inferred climate The combined data
- Page 180 and 181: Dettmann et al. (1992) have argued
- Page 182 and 183: 3. TIME SLICE K-3 Age Range: Cenoma
- Page 184 and 185: 3.2.2 North-East Australia 1. Carpe
- Page 186 and 187: 4. TIME SLICE K-4 Age Range: Turoni
- Page 188 and 189: 1. Otway Basin Limited data (Macpha
- Page 190 and 191: 5. TIME SLICE K-5 Age Range: Early
- Page 192 and 193: Inferred climate The data indicate
- Page 194 and 195: 6. TIME SLICE K-6 Age Range: Late C
- Page 196 and 197: Contrary to global cooling trends d
- Page 198 and 199: Inferred climate The relatively goo
- Page 200 and 201: Inferred climate As for regions to
- Page 202 and 203: APPENDIX 2 TERTIARY DATA 201
- Page 204 and 205: 1. TIME SLICE T-1 Age Range: Paleoc
- Page 206 and 207: also include relatively frequent No
- Page 208 and 209: Inferred climate Some differences b
- Page 210 and 211: Microfloras preserved in the Lower
- Page 212 and 213: subtropical affinities are rare, hi
- Page 214 and 215: 2. TIME SLICE T-2 Age Range: Early
- Page 216 and 217: Inferred climate Climates appear to
- Page 220 and 221: 2.2.5 Central southern Australia Ha
- Page 222 and 223: a number of distinctive Proteaceae
- Page 224 and 225: Inferred climate The Regatta Point
- Page 226 and 227: 3. TIME SLICE T-3 Age Range: Middle
- Page 228 and 229: 2. Lake Torrens Basin Abundant leaf
- Page 230 and 231: Dominance is highly variable. For e
- Page 232 and 233: types (M.K. Macphail unpubl. data).
- Page 234 and 235: Dacrycarpus), Euphorbiaceae (Austro
- Page 236 and 237: (possibly upper mesotherm) and drie
- Page 238 and 239: Basin) on the Eyre Peninsula (Alley
- Page 240 and 241: explanation is that a warm water gy
- Page 242 and 243: several taxa, which first appear in
- Page 244 and 245: 4. TIME SLICE T-4 Age Range: Oligoc
- Page 246 and 247: Inferred climate The southern limit
- Page 248 and 249: The lowest and possibly the oldest
- Page 250 and 251: Dominants include fresh to brackish
- Page 252 and 253: Based on the relative abundance of
- Page 254 and 255: (Morgan 1977, McMinn 1981a, Martin
- Page 256 and 257: common (up to 5-6%) in the middle s
- Page 258 and 259: Polypodiaceae, Palmae (Dicolpopolli
- Page 260 and 261: Strasburgeriaceae. Proprietary info
- Page 262 and 263: Rare taxa which first appear in the
- Page 264 and 265: Correlative microfloras in the onsh
- Page 266 and 267: impression of floristic impoverishm
northern New South Wales. The assemblage is dominated by monolete and trilete ferns and<br />
fern allies, associated with infrequent Casuarinaceae, Euphorbiaceae, Nothofagus and (one<br />
specimen) Tiliaceae.<br />
Inferred climate<br />
The source vegetation appears to have been fern-dominated wet scrub growing under<br />
uniformly wet (perhumid) and probably cool (lower mesotherm) conditions. Whether the<br />
cryptogam dominance reflects a recent wildfire (fire succession) or highly fertile soils<br />
(edaphic disclimax) is unknown.<br />
2.2.3 Central Australia<br />
Tertiary basins in the Alice Springs district and Lake Eyre Basin (Eyre Formation) preserve<br />
thin carbonaceous units of probable Early Eocene age (age range latest Paleocene-late Early<br />
Eocene).<br />
Many of these preserve very diverse microfloras, some of which also include dinoflagellate<br />
species that are usually associated with saline conditions (Sluiter 1991, Macphail 1996c,<br />
1997a, Alley 1998). The reason for this is unclear but salinity levels may have been raised<br />
due to discharge of saline groundwater, leaching of salt from outcrops of Early Cretaceous or<br />
older marine sediments, e.g. the Bitter Springs Formation, or deposition within<br />
hydrologically-closed basins. Microfloras from the Eyre Formation are similar to those<br />
recorded in the Late Paleocene and, apart from the absence of mangroves, are also similar to<br />
Early Eocene assemblages found in coastal northwestern Australia.<br />
1. Alice Springs district<br />
Early Eocene microfloras from the Santa Teresa and Ti-tree Basins, Alice Springs district are<br />
dominated by Casuarinaceae, Proteaceae including large (mostly described) and many small<br />
(undescribed) types, and tricolporate types. These are associated with occasional high values<br />
of monolete spores, Acrostichum-type (Cyathidites splendens), Gleicheniaceae and other<br />
trilete fern spores, and Euphorbiaceae (Malvacipollis). Araucariaceae, Dacrydium,<br />
Lagarostrobos (Phyllocladidites reticulosaccatus), Cupanieae and a member of the otherwise<br />
wholly Northern Hemisphere Triprojectites group (Integricorpus) are frequent in some<br />
samples. Rare taxa include Pteris, Lygodium, Lagarostrobos, Palmae (Arecipites,<br />
Longapertites, Nupharipollis), Anacardiaceae (Striacolporites cf. cephalus), Anacolosa<br />
(Anacolosidites acutullus), Beauprea, Callitrichaceae, Gunnera, Ilex, Sapotaceae<br />
(Sapotaceoidaepollenites latizonatus) and Tiliaceae. Nothofagus is very rare and the records<br />
may be due to downhole contamination.<br />
2. Lake Eyre Basin<br />
Microfloras dated as Paleocene in Lake Eyre Bore 8A drillhole (Alley 1983a) are more likely<br />
to be Early Eocene, based on Myrtaceidites tenuis and Proteacidites pachypolus, which first<br />
occur in the Gippsland Basin in the Lower Malvacipollis diversus Zone. The assemblages are<br />
dominated by small angiosperm pollen types (possibly Cunoniaceae, Elaeocarpaceae)<br />
associated with Gleicheniaceae, Cupressaceae, Podocarpaceae (Dacrydium, Lagarostrobos,<br />
Microcachrys, Podocarpus-Prumnopitys), Ascarina, Casuarinaceae, Euphorbiaceae,<br />
Myrtaceae, Nothofagus (Nothofagidites flemingii), and diverse Proteaceae.<br />
Pollen data from the Muloorina-2 and Poonarunna-1 wells (Sluiter 1991) hint that Myrtaceae,<br />
Proteaceae, a wholly extinct lineage of Lagarostrobos (Phyllocladidites reticulosaccatus) and<br />
Podocarpus-Prumnopitys expanded at the expense of Cunoniaceae, Cupressaceae-<br />
217