Lalith Rajapakse

The effect of summer harvesting of Phragmites australis on growth characteristics and rhizome resource storage.

The effect of harvesting the aboveground biomass on the growth of Phragmites australis in the subsequent growing season was investigated following cutting in June or July. Seasonal changes in rhizome biomass and total nonstructural carbohydrate (TNC) in seven age categories, from newly formed to six-years-old, were monitored for the two treatment stands and a control stand. The growth of the stands, as indicated by the aboveground biomass, showed a significant decline due to cutting in June but did not show a significant difference due to cutting in July, compared to that of the control stand. The timing of harvesting of aboveground biomass affected the annual rhizome resource allocation. A similar trend was observed for the pattern of resource allocation, as described by biomass variation of different rhizome-age categories for July-cut and control stands. However, the biomass of June-harvested rhizome categories tended to be smaller than the other two stands, indicating substantially reduced resource storage as a direct result of harvesting the aboveground biomass during the previous growing season. This implies that cutting of aboveground biomass in June is a better option for control of P. australis stands than cutting later in summer.

Growth dynamics and biomass allocation of Eleocharis sphacelata at different water depths: observations, modeling, and applications

Imbalanced biomass allocation patterns in emergent aquatic plants to above and below-ground structures as a response to climatic variations and water depth were investigated on the basis of observation of three stable homogeneous populations established under different water regimes and climatic environments in Goulburn and Ourimbah, New South Wales, Australia, from August 2003 to December 2004. The growth of shoots depended on water inundation-drawdown patterns and climatic variations. Shoot density was greater in shallow water but with shorter shoot length and less maximum above-ground biomass density than for plant stands in deep water. Deep-water populations attained higher below-ground biomass with higher above to below-ground biomass ratio than for the shallow-water population. Translocation of carbohydrate reserves between above and below-ground organs in deep-water populations were mostly downward throughout the year whereas the depletion–recharge pattern varied seasonally in shallow water populations. Shoots of deep-water populations grew year-round whereas in shallow water shoots died off after recession of the water level with no re-growth afterward, showing that Eleocharis sphacelata is better adapted to deep water and is stressed under shallow-water conditions. A mathematical model was formulated to describe the growth patterns of E. sphacelata and subsequently to predict the effect of water depth on production. Model simulations are in satisfactory agreement with observed patterns of growth. The model also predicts that maximum production decreases sharply with increasing water depth.

Effects of water depth and litter accumulation on morpho-ecological adaptations of Eleocharis sphacelata

The morpho-ecological adaptations of Eleocharis sphacelata in response to water depth and the sequential effects of resultant differences in deep water conditions on the long term population dynamics were investigated based on the observations carried out in three stable homogeneous populations in Goulburn and Ourimbah, New South Wales, Australia from August 2003 to May 2005. The deep water populations attained a higher harvestable shoot biomass and a lower rhizome biomass with increased growth in root structure thus significantly enhancing the nutrient uptake rates leading to a higher accumulation of shoot bound macronutrients. However, the accretion of excessive amounts of autogenous shoot litter coupled with slower decomposition rates under anaerobic conditions in the two deep water populations led to higher nutrient enrichment in sediments and overlying water column causing subsequent eutrophication with signs of growth inhibition including typical stress symptoms like stunted growth and chlorotic shoots. The shallow water population that intermittently experienced alternative inundation-drawdown pattern depicted an unaffected continuation of seasonal growth affirming that strict water regime management practices coupled with timely mowing or the removal of accumulating litter are necessary to ensure long-term survival of healthy E. sphacelata stands when it is used in applications where deep water conditions prevail.

Nutrient sources for charophytes and Najas marina in Myall Lake, Australia, indicated by carbon and nitrogen stable isotope ratios

Submerged macrophytes can assimilate mineral nutrients through both shoots and roots (MARSHNER 1995). Several studies have addressed the relative importance of roots and shoots in nutrient uptake by submerged plants (BARKO et al. 1991). The availability and form of nutrients in the surrounding water and in the interstitial water affect the plant nutrient uptake rates (CARIGNAN 1982). CEDERGREEN & MADSEN (2003) reported higher nitrate reductase activity in roots than in shoots. Stable isotope techniques have recently been used effectively to investigate the interactions of plants with their biotic and abiotic environment (DAwsoN et al. 2002). The preferential uptake of the lighter isotope by a plant and the availability of sources lead to isotope discrimination (DAwsoN et al. 2002, FRY 2006). Thus, stable isotope ratios are efficient indicators ofthe abundance of carbon and nitrogen sources for plants (FRy 2006). W e analyzed the carbon and nitrogen stable isotope ratios of benthic macrophytes from various sites in an oligohaline shallow lake to identify: (l) the nutrient sources for the plants under different conditions, (2) the preferential uptake of the lighter isotopes, and (3) the effect ofthe morphological characteristics of different plant species on nutrient uptake.