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OFR 151.pdf - CRC LEME

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Polypodiaceae, Palmae (Dicolpopollis), Casuarinaceae, Cupanieae, Ericales, Ilex,<br />

Loranthaceae, Myrtaceae (including Eucalyptus), Proteaceae (Banksia/Dryandra, Beauprea,<br />

Embothrium, Xylomelum occidentale-type), Quintinia, Trimeniaceae and Winteraceae.<br />

b. Late Early to early Late Miocene<br />

Canthiumidites bellus Zone Equivalent microfloras are more widespread on the Southeastern<br />

Highlands. Sites for which detailed microfloral information is available are Elands (M.K.<br />

Macphail unpubl. results), Kiandra at about 1400 m elevation (Owen 1988), and Palaeolake<br />

Bunyan, at about 780 m elevation near Cooma (Tulip et al. 1982). Dating of the last site is<br />

insecure due to lack of age-diagnostic taxa.<br />

The Elands microflora is dominated by Casuarinaceae (29%), Araucaria (14%), Dacrycarpus<br />

(13%), with lesser amounts of Nothofagus (Lophozonia) spp. (5%) spp., Podocarpus-<br />

Prumnopitys (4%), Blechnaceae (8%) and Cyathea (7%). Nothofagus (Brassospora) spp. are<br />

uncommon (2%). The diversity is moderately high, with some 17 cryptogam, 6 gymnosperm<br />

and 40 angiosperm species being recorded. Modern affinities range from cool temperate, e.g.<br />

Dicksonia, Lophosoria and Winteraceae, to warm temperate-subtropical, e.g. Pteris, Palmae<br />

(Dicolpopollis), Caesalpinaceae, Cupanieae, Euphorbiaceae (Mallotus-type), Malpighiaceae,<br />

Mimosaceae (Acaciapollenites miocenicus) and Rubiaceae (Guettarda, Randia).<br />

Microfloras preserved some 4 degrees to the south, at Palaeolake Bunyan and Kiandra, are<br />

dominated by Nothofagus (Brassospora) spp. (maximum values 65% and 80%, respectively).<br />

Sporadically common to abundant taxa are (maximum values in parentheses): Sparganiaceae<br />

(29%), Nothofagus (Fuscospora) spp. (17%), Nothofagus (Lophozonia) spp. (15%), Ericales<br />

(23%), Podocarpus-Prumnopitys (16%), an extinct form of Microcachrys (Podosporites<br />

microsaccatus) (55%), Blechnaceae (31%) and an unidentified inaperturate type (42%).<br />

Araucariaceae (Araucaria, Wollemi-type), Phyllocladus and Casuarinaceae are relatively<br />

uncommon (1-9%). Sporadically common taxa are Kiandra are Gleicheniaceae (47%), trilete<br />

types (16%), Dicksonia (7%) and non-eucalypt Myrtaceae (9%). Whilst the cryptogam and<br />

gymnosperm components are moderately diverse, ‘thermophilous’ taxa only occur in trace<br />

numbers and then only in one to few occasional sample, e.g. Ilex and (Kiandra) Cupanieae,<br />

Mallotus-type, Randia and Sapotaceae.<br />

The data imply rainforest communities at high elevations remained dominated by Nothofagus<br />

(Brassospora) spp. throughout the Oligo-Miocene but it is uncertain whether these were<br />

forest or wet scrub.<br />

Inferred climate<br />

Climates at lower elevations in the north of the area (Elands) are likely to have been weakly<br />

seasonal whilst mean air temperatures were adequate (upper mesotherm range) to support a<br />

form of araucarian (dry) rainforest which included palms. Climates at higher elevations in the<br />

south of the area were relatively cool (lower mesotherm range) and uniformly wet to very wet<br />

(perhumid). Despite its lower elevation, the Palaeolake Bunyan microfloras are distinctly less<br />

temperate than those recovered at Kiandra. Possible reasons are that vegetation around the<br />

former (a very large deep lake) was shaped by cold air drainage or that the microfloras postdate<br />

the mid Miocene thermal maximum.<br />

5. South-west slopes of New South Wales<br />

Microfossil evidence from the Southeastern Highlands is complemented by analyses of<br />

correlative sediments in broad river valleys draining the south-west slopes, e.g. the Lachlan<br />

Valley (Martin 1973, 1987, 1991b). Nothofagus (Brassospora) spp., which are abundant<br />

during P. tuberculatus Zone Equivalent time, are replaced by Myrtaceae as the dominant<br />

257

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