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Fig. 9.4 Tree ferns (Dicksonia sp.) with resprouting of apical meristem following high-intensity
crown fire in Eucalyptus forest of Victoria, Australia. (Photo by Jon Keeley.)
occurrence in woody dicots, and its presence in Mesozoic gymnosperm lineages
such as Ephedra , Ginkgo biloba , Sequoia sempervirens and Wollemia nobilis .
Evidence for resprouting as a fire adaptation is often of the form of plant life
histories consistent with a fire origin, although not mutually exclusive of all other
factors. For example, ferns are a lineage with widespread resprouting in response
to fire, and some lower Cretaceous fern floras appear to have consistently been
associated with fire (Harris 1981 ; Scott 2000 ). The contemporary Pteridium
aquilinum is a worldwide fire-resilient species that resprouts after burning under
a wide range of tropical and temperate habitats (Gliessman 1978 ) and there is little
reason to interpret this as an exaptation to some other environmental factor.
Gleichenia is another taxon that has been associated with fire in Cretaceous
(Herendeen & Skog 1998 ), Cenozoic (Collinson 2002 ), and Holocene environ-
ments (Black &Mooney 2006 ), and resprouts vigorously (Gillison 1969 ), as well as
recruiting from spores following fires (Walker & Boneta 1995 ). Tree ferns (e.g.
Dicksonia spp.) persist today in the understory of Australian Eucalyptus forests
and survive high-intensity crown fires, with thick overlapping leaf bases protecting
the trunk and allowing postfire resprouting from the apical meristem ( Fig. 9.4 ).
The lineage is deeply rooted in the Mesozoic and the widespread existence of fire
evidence from these early forests in association with this and other fern taxa
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