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OFR 151.pdf - CRC LEME

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SECTION 8 (CONCLUSIONS)<br />

Climatic inferences for each of the eleven Cretaceous and Tertiary time slices and seven<br />

geographic regions are summarised in Tables 8a and 8b, respectively. These inferences<br />

represent highly simplified versions of the data presented in Appendices 1-3 and summarised<br />

in Sections 3-8 and must be treated as working hypotheses for reasons given in the<br />

Introduction and re-iterated below:<br />

• Each of the seven geographic regions almost certainly encompassed a wide range of<br />

bioclimates at any particular period within the Cretaceous and Tertiary.<br />

• Each of the eleven time slices almost certainly encompassed a number of shorter-term<br />

climatic excursions imposed upon the longer term climatic trends.<br />

• Many of the sedimentary sequences and spot samples represent very short intervals of<br />

geological time.<br />

• The fossil floras are strongly biased towards species living in mesic (environmentally<br />

complacent) habitats, in particular plants living on coastal plains (fluvio-deltaic<br />

environments) and along the shorelines of lakes or riverbanks. Plants living in<br />

interfluve habitats are less likely to be represented in the fossil record. The relative<br />

representation of plants that produce and widely disperse miospores in very large<br />

numbers is exaggerated in large/deepwater lakes and analogous marine environments<br />

(Neves Effect).<br />

• The distribution of living plants (NLRs) provides only a general guide to the ecology<br />

of fossil taxa, due to the climatically forced extinction of many genera, species and<br />

ecotypes (most gymnosperms, ferns and fern allies) or adaptive radiation into novel<br />

environments (many woody angiosperms and herbs). It is emphasised that none of<br />

the NLRs of plants forming the Cretaceous to Paleocene vegetation in high to polar<br />

latitudes are adapted to prolonged winter darkness under mild (upper microthermlower<br />

mesotherm) conditions. Accordingly it is reasonable to assume that the<br />

ecophysiological adaptations of these taxa to thermal and water stresses were<br />

different from the presumed living relatives.<br />

• Shorter-term trends in community composition and structure almost certainly reflect<br />

forcing factors other than rainfall and temperature. The more important of these are<br />

low light intensities during the Cretaceous and strongly leached, infertile soils during<br />

the Tertiary. The role of volcanism and wildfires is less clear although both were part<br />

of the Cretaceous and Tertiary environments.<br />

Irrespective of the mostly low taxonomic and ecological resolution, the palaeobotanical (and<br />

related) evidence is adequate to infer qualitative long-term trends in the Early Cretaceous,<br />

Late Cretaceous and/or Tertiary climate for many regions of Australia with moderate<br />

confidence.<br />

8.1 Results in retrospect<br />

8.1.1 Palaeoclimatic records<br />

• Long-term trends correspond well with changes in global climate documented<br />

elsewhere. Anomalies such as the persistence of very warm to hot conditions at high<br />

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