OFR 151.pdf - CRC LEME
OFR 151.pdf - CRC LEME
OFR 151.pdf - CRC LEME
You also want an ePaper? Increase the reach of your titles
YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.
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 />
111