Completed projects and reports

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Sugar Research Australia, Sugar Research Development Corporation and BSES reports from completed research projects and papers.

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Author: search.filters.author.Robertson, LNSubject: search.filters.subject.Crop management

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    Statewide adoption of best irrigation practices for supplementary and full irrigation districts : SRDC Final report BS183S
    (2000) Robertson, LN; Giblin-Davis, RM; Oehlschlager, AC; Gries, R
    Project BS183S has researched and identified a number of means by which on-farm water use efficiency may be improved. These include the use of irrigation scheduling devices, improved furrow irrigation design and management, and use of modelling tools by local extension staff.Field trials demonstrated that deep drainage losses associated with furrow irrigation can be reduced by the use of surge irrigation and improved furrow irrigation management. Use of the furrow irrigation simulation model SIRMOD has enabled advisory staff to measure and optimise furrow irrigation events under typical sugar growing conditions. Difficulties however remain with deep drainage losses from furrow irrigation under trash blankets. Capacitance soil moisture meters and tensiometers were demonstrated to be effective tools for scheduling sugarcane irrigation. These devices enable growers to time irrigations to minimise crop water stress. APSFront~Sugar was developed in conjunction with APRSU to enable local advisory staff to investigate a range of issues related to sugarcane production. Despite difficulties with high rainfall, field trials demonstrated that in the absence of watertables APSIM produced reasonable predictions of crop yield. APSIM was employed to determine effective rainfall, crop response to irrigation, water use efficiency and irrigation requirement for the Mackay, Bundaberg, Mareeba, Proserpine, Atherton, Childers, and Sarina districts. APSIM was also able to identify a number of improved strategies for the use of limited allocation in supplementary irrigation districts. Project BS183S provided considerable training and support to research and extension staff.
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    Key factors in control of Greyback Canegrub populations : SRDC final report BS120S
    (BSES, 1998) Robertson, LN; Dall, DJ; Lai-Fook, J; Kettle, CG; Bakker, P
    Greyback canegrub outbreaks with severe losses in sugar production have persisted for more than six years in the Burdekin district, but population densities of the pest have declined at locations in the Herbert Valley, Tully and Innisfail districts over the same period. Six species of pathogenic organism were found to cause disease and death of greyback canegrubs, with relatively high incidence in grubs collected from the Herbert Valley, Tully and Innisfail study sites, but low incidence in the Burdekin. No deaths from entomopathogenic diseases were recorded in 226 grubs examined from the Burdekin in 1998. Two microorganisms, Adelina sp (Protozoa: Coccidia), and Metarhizium anisopliae (Deuteromycetes fungi), were the most prevalent pathogens in far north Queensland grub populations. Incidence of Adelina sp. alone accounted for 55-64 % of the variance in mortality of grubs recorded from samples collected across all locations in 1994 and 1995. The initial objectives of this SRDC funded study were to study dispersion of greyback canegrubs in the soil profile and devise a sampling program to estimate population density with known precision; monitor population density of greyback adults, eggs and larvae; identify mortality factors which act on each life stage including climate, natural enemies and farming practices; determine key factors which control greyback population changes and suggest ways to suppress population growth; develop model which predicts changes in greyback populations. Following a review in April 1995 the project was expanded to encompass the following additional objectives; assess the effects of crop management strategies on frequency of occurrence of diseases in greyback canegrubs; demonstrate pathogenicity of selected microorganisms to greyback grubs; determine dose/response relationships (ie infectious dose, time to death, effects on larval feeding and growth); attempt small-scale in vitro culture of selected microorganisms which display pathogenicity to grubs.