Western Australian growers are adopting no-tillage farming systems, which have a greater reliance on integrated weed management systems that include competitive cultivars, high seeding rates, strategic fertilizer placement, and narrow row spacing. At the same time, they are sowing more of their barley area to cultivars with a semidwarf habit. This study compared six two-row, spring malting barley cultivars with different morphological traits at two dates of planting and three crop densities, with nil-added and added rigid ryegrass at five sites. Four cultivars, ‘Buloke’, ‘Flagship’, ‘Hamelin’, and ‘Vlamingh’, had an erect early growth habit; the other two, ‘Baudin’ and ‘Gairdner’, had a prostrate, semidwarf early growth habit. Increasing the density of rigid ryegrass plants from 16 to 125 plants/m2decreased barley grain yield by reducing crop biomass production, tiller number, grain number, and harvest index. Average grain weight was also reduced at most sites. The impact of competition on grain yield varied across sites and cultivars, but did not interact with date of planting. Baudin, Flagship, and Hamelin were more competitive with rigid ryegrass than Buloke, Gairdner, and Vlamingh. Differences in competitiveness between cultivars did not appear to be strongly related to morphological traits that affect light interception such as canopy closure, plant height, and tiller number. Differences in cultivar competitiveness were cultivar-specific and not generic. Rigid ryegrass productivity (dry matter and tiller number) tended to be lower under the more competitive cultivars. Increasing barley plant density increased grain yield, and reduced both rigid ryegrass dry matter and tiller number. Barley density had a larger impact on rigid ryegrass productivity than crop cultivar. The impact of barley density on reducing rigid ryegrass tiller number was larger with the first planting date than the second, and higher in the added rigid ryegrass plots than the nil-added plots. This study highlights the importance of high barley seeding rate for the integrated management of rigid ryegrass.
The demethylase inhibitor (DMI) or group 3 fungicides are the most important class of compounds for the control both of plant and human fungal pathogens. The necrotrophic fungal pathogen Pyrenophora teres f. sp. maculata (Ptm), responsible for spot form of net blotch (SFNB), is currently the most significant disease of barley in Australia, and a disease of increasing concern worldwide. The main basis for management of SFNB is by fungicide application, and in Australia the DMIs predominate. Although reduced sensitivity to DMI fungicides has recently been described in the closely related pathogen P. teres f. sp. teres (Ptt), the mechanisms of DMI resistance have not thus far been described for Ptm. In this study, several different levels of sensitivity to DMI fungicides were identified in Western Australian strains of Ptm from 2016 onwards, and reduced sensitivity phenotypes were correlated with a number of distinct mutations in both the promoter region and coding sequence of the DMI target gene encoding cytochrome P450 sterol 14α-demethylase (Cyp51A). Five insertions elements of 134-base pairs in length were found at different positions within the upstream regulatory region of Cyp51A in both highly DMI-resistant (HR) and select moderately DMI-resistant (MR1) Ptm isolates. The five insertion elements had at least 95% sequence identity and were determined to be Solo-LTR (Long Terminal Repeat) elements, all deriving from Ty1/Copia-family LTR Retrotransposons. The 134-bp elements contained a predicted promoter sequence and several predicted transcription factor binding sites, and the presence of an insertion element was correlated with constitutive overexpression of Cyp51A. The substitution of phenylalanine by leucine at position 489 of the predicted amino acid sequence of CYP51A was found in both HR and select moderately DMI-resistant (MR2) Ptm isolates. The same F489L amino acid substitution has been previously reported in Western Australian strains of Ptt, where it has also been associated with reduced sensitivity to DMI fungicides. In Ptm, the F489L amino acid change was associated with either of three different single nucleotide polymorphisms in codon 489. This suggests that, in contrast to Ptt, in Ptm the F489L mutation has emerged as a result of three distinct mutational events. Moderately DMI-resistant isolates had one or the other of the F489L substitution or a promoter insertion mutation, whereas highly DMI-resistant isolates were found to have combinations of both mechanisms together. Therefore, multiple mechanisms acting both alone and in concert were found to contribute to the observed phenomena of DMI fungicide resistance in Ptm. Moreover, these mutations have apparently emerged repeatedly and independently in Western Australian Ptm populations, by a process of convergent or parallel evolution.
Summer crops grown during the summer fallow in a Mediterranean-type climate have the potential to produce out-of-season biomass and grain, increase water use, and reduce deep drainage. The potential effects of growing grain sorghum on components of the water balance, sorghum biomass and grain production, and yield of subsequent wheat crops were investigated by simulation using APSIM and long-term climate data from the Esperance district. Sorghum was simulated as part of 3 systems: (1) as an opportunity crop following wheat harvest, (2) as a fallow replacement after pasture removal and before entering a cropping phase, or (3) as a fallow replacement after a failed or waterlogged winter crop. Simulations were conducted for the period 1957–2003 at Myrup (mean annual rainfall 576 mm), Scaddan (408 mm), and Salmon Gums (346 mm). Sorghum was assumed to have a similar rooting depth to wheat. In order to gain confidence in using APSIM for these investigations, tests were initially conducted against field data involving summer and winter crops in sequence and measurements of soil water dynamics. Data sets also varied in summer rainfall, species (forage sorghum, grain sorghum, Japanese millet), and soil type (deep sand, and medium and shallow duplex). Overall, the simulations showed that incorporation of a sorghum crop increased transpiration by 10–30 mm/year, made the soil profile drier by a similar amount at wheat sowing, and consequently reduced deep drainage by 3–25 mm/year, depending upon cropping system and location. Long-term average drainage results were dominated by large episodes in wet years. The increased transpiration from the summer crop, although reducing drainage in wet years, could not eliminate drainage. Following wheat yields were reduced by an average of 200–400 kg/ha, corresponding to a reduction of 10% at wetter and 30% at drier locations. In the 2 fallow replacement systems, sorghum biomass was produced in nearly every simulated season. However, averaged over all seasons, sorghum grain production was much less reliable comprising only 10–20% of biomass. In the opportunity system, sorghum produced biomass in only 1 in 3 seasons at Salmon Gums and Scaddan and 1 in 2 at Myrup. Grain was produced in 1 in 5 seasons at all 3 locations, underlining the riskiness of this opportunity niche for summer crops in the Esperance district. Although summer cropping was shown to result in modest reductions in deep drainage, it also comes at a cost to wheat production. The largest effects on drainage and most reliable biomass production were seen in the systems where the summer crop was grown following pasture removal or a failed (waterlogged) winter crop. This research has also shown that recent farmer and researcher experiences of summer cropping are likely to be more favourably biased towards prospects for summer cropping than indicated by long-term simulations because of their longer-term perspective.
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