Search

Water use and depth of water extraction of leucaena (Leucaena leucocephala) and Rhodes grass (Chloris gayana) pasture, irrigated with desalinated coal seam water (a by-product of the coal seam gas industry), were monitored to provide background information on root activity, spatial and temporal water use and deep drainage over a 757-day period from August 2011 to August 2013. Methodology comprised measurement of soil water from surface to 4 m depth using 8 EnviroSCAN probes connected to dataloggers positioned within leucaena twin rows and within the Rhodes grass inter-row. Just over 581,000 individual moisture measurements were collated and are reported here. Water extraction (and by inference root activity) of leucaena and Rhodes grass showed marked seasonal fluctuation with deepest and highest water extraction occurring during the first growing season; water extraction was greatly diminished during the following drier and cooler seasons due to the negative influences of lower soil moisture contents, lower temperatures and increased defoliation on pasture growth. The highest values of deep drainage below 4 m depth occurred when high rainfall events corresponded with high soil water storage in the entire profile (0–4 m depth). Given that water usage by both leucaena and Rhodes grass was greatest in the upper layers of soil (Keywords: Active rooting depth, agroforestry, Chloris gayana, Leucaena leucocephala, water extraction.DOI: 10.17138/TGFT(4)129-138

Soil nitrification (microbial oxidation of ammonium to nitrate) can lead to nitrogen leaching and environmental pollution. A number of plant species are able to suppress soil nitrifiers by exuding inhibitors from roots, a process called biological nitrification inhibition (BNI). However, the BNI activity of perennial grasses in the nutrient-poor soils of Australia and the effects of BNI activity on nitrifying microbes in the rhizosphere microbiome have not been well studied. Here we evaluated the BNI capacity of bermudagrass (Cynodon dactylon L.), St. Augustinegrass (Stenotaphrum secundatum (Walt.) Kuntze), saltwater couch (Sporobolus virginicus), seashore paspalum (Paspalum vaginatum Swartz.), and kikuyu grass (Pennisetum clandestinum) compared with the known positive control, koronivia grass (Brachiaria humidicola). The microbial communities were analysed by sequencing 16S rRNA genes. St. Augustinegrass and bermudagrass showed high BNI activity, about 80 to 90% of koronivia grass. All the three grasses with stronger BNI capacities suppressed the populations of Nitrospira in the rhizosphere, a bacteria genus with a nitrite-oxidizing function, but not all of the potential ammonia-oxidizing archaea. The rhizosphere of saltwater couch and seashore paspalum exerted a weak recruitment effect on the soil microbiome. Our results demonstrate that BNI activity of perennial grasses played a vital role in modulating nitrification-associated microbial populations.