Paul Weston

Dr. Paul Weston

School of Agricultural and Wine Sciences and Graham Centre for Agricultural Innovation, Charles Sturt University, Wagga, NSW 2678, Australia
orcid

Research Focus & Metrics

Academic Career Length

42Years (1985-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 April 2000 in Journal of Economic Entomology
Verified
Journal Article
Closed access
PDF file
Paul WestonPaul Weston
Paul Weston
PRPatti L. Rattlingourd
Patti L. Rattlingourd
A laboratory experiment was conducted to quantify the effects of infestation of maize by Sitotroga cerealella (Olivier) on progeny production by two common seco

18 May 2016 in Journal of Experimental Botany
Verified
Journal Article
Open access
PDF file
XZXiaocheng Zhu
Xiaocheng Zhu
DSDominik Skoneczny
Dominik Skoneczny
JWJeffrey D. Weidenhamer
Jeffrey D. Weidenhamer
James M MwendwaJames M Mwendwa
James M Mwendwa
Paul WestonPaul Weston
Paul Weston
Leslie Ann WestonLeslie Ann Weston
Leslie Ann Weston
Bioactive plant secondary products are frequently the drivers of complex rhizosphere interactions, including those with other plants, herbivores and microbiota. These chemically diverse molecules typically accumulate in a highly regulated manner in specialized plant tissues and organelles. We studied the production and localization of bioactive naphthoquinones (NQs) in the roots of Echium plantagineum, an invasive endemic weed in Australia. Roots of E. plantagineum produced red-coloured NQs in the periderm of primary and secondary roots, while seedling root hairs exuded NQs in copious quantities. Confocal imaging and microspectrofluorimetry confirmed that bioactive NQs were deposited in the outer layer of periderm cells in mature roots, resulting in red colouration. Intracellular examination revealed that periderm cells contained numerous small red vesicles for storage and intracellular transport of shikonins, followed by subsequent extracellular deposition. Periderm and root hair extracts of field- and phytotron-grown plants were analysed by UHPLC/Q-ToF MS (ultra high pressure liquid chromatography coupled to quadrupole time of flight mass spectrometry) and contained more than nine individual NQs, with dimethylacrylshikonin, and phytotoxic shikonin, deoxyshikonin and acetylshikonin predominating. In seedlings, shikonins were first found 48h following germination in the root-hypocotyl junction, as well as in root hair exudates. In contrast, the root cortices of both seedling and mature root tissues were devoid of NQs. SPRE (solid phase root zone extraction) microprobes strategically placed in soil surrounding living E. plantagineum plants successfully extracted significant levels of bioactive shikonins from living roots, rhizosphere and bulk soil surrounding roots. These findings suggest important roles for accumulation of shikonins in the root periderm and subsequent rhizodeposition in plant defence, interference, and invasion success.

1 January 2015
Verified
Book
Closed access
JMJames R. Miller
James R. Miller
CAChristopher G. Adams
Christopher G. Adams
Paul WestonPaul Weston
Paul Weston
JSJeffrey H. Schenker
Jeffrey H. Schenker

1 March 1997 in Aquaculture
Verified
Journal Article
Closed access
JTJames H Tidwell
James H Tidwell
SCShawn D Coyle
Shawn D Coyle
CWCarl D Webster
Carl D Webster
JSJohn D Sedlacek
John D Sedlacek
Paul WestonPaul Weston
Paul Weston
MFMarty J Fuller
Marty J Fuller

6 May 2011 in Ecological Entomology
Verified
Journal Article
Closed access
PDF file
GDGaylord A. Desurmont
Gaylord A. Desurmont
Paul WestonPaul Weston
Paul Weston

9 July 2020 in Agronomy
Verified
Journal Article
Open access
PDF file
James M MwendwaJames M Mwendwa
James M Mwendwa
WBWilliam B. Brown
William B. Brown
Jeffrey WeidenhamerJeffrey Weidenhamer
Jeffrey Weidenhamer
Paul WestonPaul Weston
Paul Weston
JQJane Quinn
Jane Quinn
Leslie Ann WestonLeslie Ann Weston
Leslie Ann Weston
Herbicide resistance in weeds restricts control options, thereby escalating economic loss and threatening agricultural sustainability in cereal production. Field evaluation of the crop performance, competitive traits, and consequent weed suppressive potential of 13 commercial winter wheat (Triticum aestivum L.) cultivars was performed in central NSW Australia with a focus on the evaluation and modelling of above-ground interactions. In 2015 and 2016, replicated field trials were established with genetically diverse commercial wheat genotypes under moderate to low rainfall conditions in Wagga Wagga (572 mm) and Condobolin (437 mm) New South Wales, respectively. The heritage cultivar Federation and a commercial cultivar of winter cereal rye (Secale cereale L.) were included as known weed-suppressive controls. Crop and weed growth, as well as early vigour, leaf area index, and photosynthetically active radiation, were monitored at various crop phenological stages including early growth, vegetative, flowering, grain fill, and harvest. Significant differences between wheat cultivar and location were observed for crop biomass, early vigour, leaf area index, weed number, weed biomass, canopy architecture, and yield in both 2015 and 2016. Differences in weed establishment were largely impacted first by rainfall and season and secondly by crop architecture (i.e., height, size, canopy) and phenology (i.e., growth stages). Early vigour and early canopy closure were instrumental in suppressing weed establishment and growth. Cultivar performance and competition with weeds were also clearly influenced by both environmental factors and genotype, as evidenced by differences in early cultivar performance, yield, and weed suppression by season and location. Specifically, Federation, Condo, and Janz wheat cultivars were superior performers in terms of weed suppression in both locations and years; however, Federation produced up to 55% lower yield than recently introduced cultivars. Partial least squares (PLS) regression was performed to develop a predictive linear model for weed competition in commercial wheat cultivars based on weed dry biomass as the response variable and selected aboveground crop canopy traits as predictors. In 2015, the model differed in accordance with crop growth stage, but the impact of predictors on weed biomass at both locations was not significant. In 2016, under local above average rainfall conditions, the model showed a significant negative correlation (p < 0.001) of most predictors on weed biomass (r2 = 0.51 at Condobolin, r2 = 0.62 at Wagga Wagga), suggesting the most influential factors in reducing weed numbers and establishment as crop vigour, biomass, and height. Our results indicate the establishment of competitive wheat cultivars in the absence of post-emergent herbicides resulted in a two to five-fold increased weed suppression over less suppressive genotypes, without significant yield penalties. Therefore, cultivar choice constitutes a cost-effective and sustainable weed management tool, particularly when weed pressure is significant.