There are saltmarshes on either side of the Mandurah channel, on the eastern
side of Peel Inlet and around the southern part of Harvey Estuary. Narrow fringing
marshes also border the Serpentine River (DCE,
1980).
The sediments that build saltmarshes originate from upland runoff, marine reworking
of coastal shelf sediments, and organic production within the marsh itself.
The long-term stability of a saltmarsh is determined by the relative rates of
two processes acting on the marsh: sediment increase or accretion,
which causes the marsh to expand outward and grow upward in the intertidal zone;
and by loss, or submergence, caused by rising sea level and marsh surface subsidence
(Allen & Pye, 1992).
Although physical processes dominate sediment accretion,
the effects of plants and animals can also be significant. Algae have an important
role in the stabilisation of mudflats, which can then be colonised by flowering
plants. These plants then slow water movement, allowing sediment in the water
to accrete in the marsh, where it can be trapped by algal, bacterial and diatom
mats (Adam, 1993).
Saltmarshes act as a buffer to the intertidal zone. Erosion of the surface of the marsh and its edges protects the shore behind it from erosion by high-energy waves. Saltmarsh creeks also allow the dissipation of tidal energy, which would otherwise erode the mudflats and the shoreline behind them (Allen & Pye, 1992).
Tides influence a wide range of physical and chemical processes. These processes in turn influence the species in the marsh and their growth. The lower and upper limits of the marsh are generally set by the tidal range. In fact, the marsh is often divided into two zones, the upper (or high) marsh and the lower (or intertidal) marsh. The upper marsh is flooded irregularly and has a minimum of ten days of continuous exposure to the air, whereas the lower marsh is flooded almost daily (Allen & Pye, 1992; Adam, 1993).
A notable feature of saltmarshes, and especially the low marsh, is the development of pans and tidal creeks. The term 'pan' is used to describe shallow depressions in the marsh which are filled periodically with water (Plate 1.2). They range from half a metre to several metres in width and a few centimetres to a half a metre deep. Because of their shallow depth and occasionally submerged vegetation, pans are used extensively by migratory wading birds searching for food. Tidal creeks, another feature of saltmarshes, serve as important conduits for material and energy transfer between the marsh and the adjacent body of water (Allen & Pye, 1992).
The development and zonation of vegetation in a saltmarsh are influenced by several chemical factors. Salinity of the overlying water and soil water is a dominant factor determining the species present and their rate of growth. Salinity is affected by the frequency of tidal inundation; rainfall; soil texture; vegetation; depth of water table; fresh water inflow; and occurrence of salt deposits (Montague & Wiegert, 1991; Adam, 1993).
As the elevation of a marsh surface increases, the number of flooding tides decreases. This may be expected to result in decreased salinity, but the salinity of the interstitial soil water does not have a constant relationship with elevation. In the lower marsh, with frequent immersion, soil salinity is relatively constant and rarely exceeds that of the flooding water. At higher elevations there is a stronger interaction between flooding and climate, leading to greater variability in soil salinity (Adam, 1993).
Soils of the saltmarsh are frequently waterlogged and anaerobic. After tidal
immersion many areas of marsh drain slowly, as a result of local topography
and the low hydraulic conductivity of many saltmarsh soils (Adam,
1993).
Saltmarshes are often cited as exporting nutrients to the estuary, but this view has been challenged and refined in recent years. It is now believed that coastal marshes display a high degree of individuality. They are still able to fix carbon at very high rates, but the fate of this carbon is not readily predicted. Systems with large river flows are likely to transport large fractions of their net primary production during spring runoff; those systems with broad tidal amplitude may export organic matter year round; or marshes experiencing rapid sea-level rise may accumulate plant matter in the sediments; and finally small, semi-enclosed marshes may use the energy of photosynthesis to produce organic matter and recycle large portions of their fixed carbon. Thus, the high productivity is either exported as detritus, accumulated as peat, or released in respiration (Zedler, 1992).
In the Peel-Harvey system during winter and spring, there is the potential for organic matter and nutrients to be washed into the estuary from the marsh. At other times, there may be an import of organic matter and nutrients from the estuarine waters. Saltmarshes also convert nutrients into forms that can be easily absorbed by estuarine plants and animals (Mitsch & Gosselink, 1993).
The availability of nutrients in the saltmarsh soil, particularly nitrogen
and phosphorus, is important for the productivity of the saltmarsh ecosystem.
Several studies have shown that saltmarsh vegetation can be nitrogen limited
(Valiela & Teal, 1985; Barko
and Smart, 1981). Phosphorus, however, accumulates in plant tissue at relatively
high concentrations and apparently does not limit growth. Other nutrients which
may influence the productivity of the marsh are iron, manganese and sulphur
(Mitsch & Gosselink, 1993).
The saltmarsh flora is composed of bacteria, fungi, algae, and flowering plants. In general the diversity of the flora increases with elevation above sea level, which results from differences in the soil, and competition among plant species (Adam, 1993).
Bacteria and fungi are important components of saltmarsh microflora. They are responsible for breaking down plant and animal matter and transforming it into forms of nutrients available to other organisms. Fungi are also found in the soil and on the flowering plants in the higher marsh. Almost three-quarters of the detritus produced in a saltmarsh ecosystem is broken down by bacteria and fungi (Montague & Wiegert, 1991; Adam, 1993).
Algae are found attached to flowering plants, as free-living phytoplankton, and as macroalgae. The algae are important as food sources for aquatic and terrestrial animals. Algal mats, dominated by blue-green algae, diatoms and green algae are also present (Montague & Wiegert, 1991; Adam, 1993; Mitsch & Gosselink, 1993; Paling & McComb, 1994).
The flowering plants of the saltmarsh include herbs, grasses, sedges, dwarf shrubs and trees. They are dominated by halophytic flowering plants. The lower marsh is usually dominated by one species. With increasing elevation species diversity tends to increase and distinct communities of flowering plants can be recognised (Chapman, 1974; Montague & Wiegert, 1991; Adam, 1993).
In the Peel-Harvey the lower marsh is dominated by Sarcocornia quinqueflora
(samphire) with communities of Halosarcia species (grasswort), herbs
and grasses occurring with increased elevation inland. Further inland communities
of Juncus kraussii (shore rush), Melaleuca cuticularis (saltwater
paperbark) and Casuarina obesa (saltwater sheoak) occur (Figure
1.2).
The aerial habitat is dominated by insects such as grasshoppers, plant hoppers, wasps and beetles, and spiders that live in and on plant leaves. The stems and leaves of saltmarsh plants are also visited by snails. These animals make up the grazing portion of the saltmarsh food web (Figure 1.3). Large numbers of birds forage on the aerial invertebrate community, including egrets, little grassbirds, white-fronted chats, richard's pipits and Australian magpie-larks. The stems and leaves of saltmarsh plants are used as nesting material for resident saltmarsh birds such as the black-winged stilt, which build their nests sufficiently high to avoid all but the highest tides (Montague & Wiegert, 1991).
Less than 10 percent of the plant material produced each year in a saltmarsh is removed by animal grazing. Most plant biomass dies and decays on the marsh surface, and its energy is processed by fungi and bacteria. These organisms serve as a food source for microscopic animals in the decaying vegetation and on the sediment surface of the marsh. Most of these benthic organisms are protozoa, nematodes, harpacticoid copepods, annelids, rotifers, and the larval stages of macro-invertebrates (Montague & Wiegert, 1991).
Benthic macrofauna forage on the sediment or filter floodwater. The common macro-invertebrates present in the sediment include polychaetes, gastropod molluscs and crustaceans; these in turn become food for a variety of predators such as the blue manna crab and egret (Montague & Wiegert, 1991).
Aquatic animals in saltmarshes often overlap in distribution with those in the benthic habitat of the open water (Figure 1.3). Zooplankton in saltmarsh creeks and in pans are similar in species composition and abundance to those of the open estuarine waters of the marsh. These may include copepods, ostracods and chaetognaths. These animals are important food for small fish which shelter in the saltmarsh creeks and pans. The macro-invertebrates that inhabit the saltmarsh creeks and pans include fly and mosquito larvae. These larvae in turn are food for fish, wading birds, and ducks. Adult mosquitoes feed from the nectar of plants, and in doing so help to pollinate these plants (Montague & Wiegert, 1991).
Although the main fish habitat is the creek and associated marsh edge, fish
and shellfish venture from tidal creeks into the marsh when it becomes flooded.
When the water recedes, small fish may remain in pans in the marsh, where they
are often eaten by wading birds or eventually die of exposure (Montague
& Wiegert, 1991).
The Peel-Harvey estuary is one of the largest and most important wetlands for
birds in southwestern Australia. The wading birds often encountered in the saltmarshes
of the Peel-Harvey estuary include the great and little egret, the white-faced
heron, the yellow-billed spoonbill, the common sandpiper, and the red-necked
stint. Some of the waders are listed in the Japan-Australia Migratory Birds
Agreement. The marshes also support a variety of waterfowl such as the Australian
shelduck, pacific black duck and musk duck (Halse
et al, 1989; Chester &
Klemm, 1990; Ninox, 1990).
Several species of reptiles occur in the Peel-Harvey saltmarshes, the
most notorious being the common tiger snake which preys on frogs, fish,
lizards, small mammals and birds. The native mammals most likely to be
found on the saltmarshes are kangaroos and wallabies. Introduced species,
such as cats and foxes can also be found hunting birds of the marshes.
2) To examine the relationship between plant distribution and water
level, to predict the possible effects which construction of the Dawesville
Channel might have through establishing a new water regime.
3) To investigate the distribution of invertebrates in summer and winter
in the saltmarsh.
4) Recommend areas of management priority and process by which they
may be protected.
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