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The mammalian fauna consists of large browsers (wallabies,
wombats), medium-sized ground omnivores and insectivores (bandicoots,
potoroos, echidna), small ground insectivores, herbivores
and omniivores (antechinus, native
rats, native mice), small and medium-sized arboreal marsupials
(pygmy-possums, sugar gliders, possums), and bats. Most of the birds are
common woodland species, particularly those that feed near the ground (thornbills, treecreepers,
honeyeaters, scrubwrens, whistlers, rosellas, currawongs,
robins, pardalotes, cuckoos, parrots, fairy-wrens) and there are
Heathland specialists (Ground Parrot,
Bristlebird, New Holland Honeyeater).
The reptiles are mostly small ground-dwelling skinks,
legless lizards, dragons, goannas and snakes. There is a wide
range of frogs which are common in wetter areas, some of which have a
burrowing lifestyle.
Heathland is one of the oldest recognised ecosystems in the world.
The name was first applied to the the treeless vegetation of Europe
where Heather (Calluna vulgaris)
and the spiny pea, Gorse (Ulex europaeus), often make up the bulk of
the vegetation. The male and female names Heath and Heather are derived from the ecosystem and the term
Heathen
was originally coined to represent those people who lived in Heathland
away from the major townships and hence shunned mainstream Christianity.
When vegetation with a similar appearance was discovered in Victoria it
was logical that the same term would be used to describe it, even if
there were significant differences at the ecological level. It is
therefore a little ironic that while Victorian Heathlands are natural
ecosystems most of the European versions were probably created by
removing the trees from a native woodland some time during the Bronze
Age (about 3000 or more years ago) and the Heathland people maintained
the treeless landscape so they could graze their livestock.
The key ecological feature of Heathland is the extremely low nutrient
status of its soils, a feature that affects almost everything about the
way the ecosystem is inhabited. Every plant and animal that lives
within Heathland must have some adaptive mechanism for dealing with the
relative paucity of significant biological chemicals such as phosphates
and nitrates. The most obvious physical adaptation is the small
stature of most Heathland plants, which goes hand in hand with a slow
growth rate. The slow growth often overrides periodic flushes
of extra nutrients - for example, when an animal dies and decomposes or
when masses of nutrients are released after a wildfire - which are
stored in underground organs rather than utilised in increasing the size
of above-ground plant parts. The presence of large underground
woody storage organs (lignotubers) on many of the shrubs and large,
carbohydrate-rich tubers, corms and leaf bases on sedges and herbs means
that there is usually a greater mass of living tissue beneath the soil
surface than above.
Even slow growth cannot proceed unless there are mechanisms for
extracting the small amounts of nutrients from the soils and to do this
most species have adaptations associated with their root systems.
Members of the Proteaceae (Banksia,
Hakea, Grevillea) and at least one pea (Viminaria)
have the ability to generate dense clusters of fine roots, covered with
long root hairs, whenever the root system encounters pockets of
nutrients. Some sedges (Gahnia,
Lepidosperma, Schoenus) and rope rushes (Hypolaena,
Empodisma) have analogous structures designed to maximise
the root surface contact with the soil. Many other species,
especially the shrubs and small trees, utilise a symbiotic relationship
between soil fungi and roots (mycorrhizae)
to access soil nutrients. The host plant provides the fungus with
carbohydrates and in return gains access to a far-reaching network of
fine nutrient-gathering fungal threads (hyphae). Another symbiotic
relationship, this time between roots and soil bacteria, creates nodules
on the roots of some species (bush peas,
wattles, she-oaks) which can convert atmospheric nitrogen in the
soil into a form suitable for uptake into the plant. Finally, some
plants use insectivory to supplement their nitrate and phosphate intake
(Drosera, Utricularia)
while others simply resort to parasitism (Cassytha).
Fires, which are a relatively frequent event in Heathland, are an
important component of the ecosystem's ecology. They act as a means of returning nutrients to the soils
and opening the canopy for regeneration of small, ground-layer species
such as orchids, sundews, dampieras, lilies, goodenias and other herbs.
The structure of Heathland vegetation encourages these events. As
the larger shrubs age they present a greater quantity of dry branches and
fine twigs with only a relatively thin veneer of small, hard
leaves (which may themselves contain flammable oils) in the upper
canopy. After 30 to 50 years without fire the understory is
largely shaded out and is less diverse, the leaf litter (which may help
reduce the numbers of other species by releasing growth inhibitors into
the soil) becomes dense and the vegetation is extremely susceptible to
burning. Heathland fires are seldom 'hot', in the sense that the
explosive crown fires in forests can be, and they flare up and die down
very rapidly because the fuel load is never large, at least when compared to the
massive quantities of logs, dry tree trunks and oil-laden eucalypt
leaves that make up a forest.
A Heathland fire, in old vegetation during the summer, is an almost perfect
regeneration burn. The larger shrubs have most of their branches
removed but few of them die and most regenerate directly from
rootstocks and lignotubers. Those that are killed will reproduce from seed that
was held on the plant in woody capsules until after the fire (Hakea,
Banksia, Leptospermum, Allocasuarina, Melaleuca) or from
hard-cased, soil-stored seed (wattles,
bush-peas). Similarly, grass trees (Xanthorrhoea)
will sprout from their bases within days of the fire passing and the
following spring will display a uniform mass of new flowering spikes,
attracting sometimes huge flocks of parrots, lorikeets and honeyeaters.
Most sedges, coarse lilies and many herbs will regenerate in the same manner as the
grass trees providing post-fire forage for wombats and wallabies. The real excitement, however, will be the wide range
of small plants that no longer have to contend with the inhibiting
effect of a dense shrub layer and now can put up shoots, often from
semi-dormant tubers, and flower in great numbers.
Chief amongst the small plants that flourish after fires are the
ground orchids. Heathland supports a greatest proportion of
orchids of all Victorian ecosystems and many species respond quickly to
fire, indeed some are fire specialists (Pyrorchis,
Burnettia) and seldom
flower under other conditions. The first spring after a fire will
usually yield the greatest flowering events, provided there have been
adequate winter rains. In subsequent years the shrub, sedge and
rope-rush recovery will be greater and the vegetation starts to take on
a more uniform look. Nevertheless, the botanical diversity of
Heathland is greatest in the first decade after a fire and this seems to
be critical to the survival of some small mammals such as native mice (Pseudomys)
and bandicoots. These species forage on a range of seeds,
tubers, fruits, invertebrates and fungi which become fewer and more
difficult for the animals to find as the vegetation ages.
Consequently these animals will move around the ecosystem seeking out
the younger vegetation, without which local extinctions are likely.
Human use of Heathland, since European settlement, has been minimal;
in most cases the ecosystem has either been cleared or left alone.
In areas where the soils are deeper and slightly more fertile there has
been widespread clearing for marginal agriculture where application of
phosphate and nitrate fertilisers and sowing of pasture grasses has
enabled sheep grazing. In most other areas the vegetation has been
left undeveloped and, over time, many of these have been incorporated
into the park system. There are now substantial parks with
Heathland as a major component (Grampians, Croajingolong, Little Desert)
as well as many smaller reserves. Management of the vegetation has
been been a straightforward affair as weed eradication programs are
often unnecessary because of the inability of most northern hemisphere
species to invade the infertile soils. Fire management features
high on the list of priorities for Heathland reserves perhaps because
they are easy to control, due to their relatively low intensity. A
problem that has arisen from the application of fire to Heathland is
that the botanical composition of the vegetation has changed, in some
areas quite radically. Bracken (Pteridium
esculentum) often comes to dominate the understory in areas
where high-frequency burning (less than 5 years) has been applied and
especially when this has taken place during spring or autumn rather that
the, more natural, summer season. Today Bracken and Prickly
Tea-tree (Leptospermum continentale)
are the two most widespread and abundant species of Heathland, the
former because of its ability to regenerate from underground rhizomes,
the latter because of its prolific seed production and rapid germination
after fire. Both species grow in such dense thickets that much of
the understory is shaded out and the overall diversity of the ecosystem
is diminished.
The European Heather is a member of the
Ericaceae and it, along with other members of
the family, including the dry-seeded Erica (European
Heath) and the fleshy-fruited Vaccinium (Cranberry),
are small-leafed, tubular-flowered shrubs with an unusual, fine root
system that develops a mycorrhizal association peculiar to the family.
In Victorian Heathland the analogous family is the
Epacridaceae (Epacris,
Leucopogon, Astroloma, Acrotriche, Monotoca, Richea, Styphelia,
Brachyloma) which has similar tubular flowers, root systems
and mycorrhizae, and also has both dry-seeded and fleshy-fruited
species. Recently, some botanists have determined that the
similarities between the two families are so great that they should both
be merged into the older classification - that is, all should be
considered to be members of the Ericaceae. While there are
undoubtedly sound taxonomic and ecological reasons for this amalgamation
it does seem a little disappointing to lose an Australian plant family
which is characteristic of a distinctive, species-rich ecosystem.
© Paul Gullan, Viridans Biological Databases
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