Glyphosate-tolerant and glyphosate-resistant weeds are becoming increasingly problematic in cotton fields in Australia, necessitating a return from a glyphosate dominated system to a more integrated approach to weed management. The development of an integrated weed management system can be facilitated by identifying the critical period for weed control (CPWC), a model that enables cotton growers to optimize the timing of their weed control inputs. Using data from field studies conducted from 2003 to 2015, CPWC models using extended functions, including weed biomass in the relationships, were developed for the mimic weeds, common sunflower and Japanese millet, in high-yielding, fully irrigated cotton. A multispecies CPWC model was developed after combining these data sets with data for mungbean in irrigated cotton, using weed height and weed biomass as descriptors in the models. Comparison of observed and predicted relative cotton-lint yields from the multispecies CPWC model demonstrated that the model reasonably described the competition from these three very different mimic weeds, opening the possibility for cotton growers to use a multispecies CPWC model in their production systems.

Research using the critical period for weed control (CPWC) has shown that high-yielding cotton crops are very sensitive to competition from grasses and large broadleaf weeds, but the CPWC has not been defined for smaller broadleaf weeds in Australian cotton. Field studies were conducted over five seasons from 2003 to 2015 to determine the CPWC for smaller broadleaf weeds, using mungbean as a mimic weed. Mungbean was planted at densities of 1, 3, 6, 15, 30, and 60 plants m−2 with or after cotton emergence and added and removed at approximately 0, 150, 300, 450, 600, 750, and 900 degree days of crop growth (GDD). Mungbean competed strongly with cotton, with season-long interference; 60 mungbean plants m−2 resulted in an 84% reduction in cotton yield. A dynamic CPWC function was developed for densities of 1 to 60 mungbean plants m−2 using extended Gompertz and exponential curves including weed density as a covariate. Using a 1% yield-loss threshold, the CPWC defined by these curves extended for the full growing season of the crop at all weed densities. The minimum yield loss from a single weed control input was 35% at the highest weed density of 60 mungbean plants m−2. The relationship for the critical time of weed removal was further improved by substituting weed biomass for weed density in the relationship.

Field studies were conducted over five seasons from 2004 to 2015 to determine the critical period for weed control (CPWC) in high-yielding, irrigated cotton using a competitive mimic grass weed, Japanese millet. Japanese millet was planted with or after cotton emergence at densities of 10, 20, 50, 100, and 200 plants m−2. Japanese millet was added and removed at approximately 0, 150, 300, 450, 600, 750, and 900 degree days of crop growth (GDD). Data were combined over years. Japanese millet competed strongly with cotton, with season-long interference resulting in an 84% reduction in cotton yield with 200 Japanese millet plants m−2. The data were fit to extended Gompertz and logistic curves including weed density as a covariate, allowing a dynamic CPWC to be estimated for densities of 10 to 200 Japanese millet plants m−2. Using a 1% yield-loss threshold, the CPWC commenced at 65 GDD, corresponding to 0 to 7 d after crop emergence (DAE), and ended at 803 GDD, 76 to 98 DAE with 10 Japanese millet plants m−2, and 975 GDD, 90 to 115 DAE with 200 Japanese millet plants m−2. These results highlight the high level of weed control required throughout the cropping season in high-yielding cotton to ensure crop losses do not exceed the cost of weed control.

Field studies were conducted over six seasons to determine the critical period for weed control (CPWC) in high-yielding cotton, using common sunflower as a mimic weed. Common sunflower was planted with or after cotton emergence at densities of 1, 2, 5, 10, 20, and 50 plants m−2. Common sunflower was added and removed at approximately 0, 150, 300, 450, 600, 750, and 900 growing degree days (GDD) after planting. Season-long interference resulted in no harvestable cotton at densities of five or more common sunflower plants m−2. High levels of intraspecific and interspecific competition occurred at the highest weed densities, with increases in weed biomass and reductions in crop yield not proportional to the changes in weed density. Using a 5% yield-loss threshold, the CPWC extended from 43 to 615 GDD, and 20 to 1,512 GDD for one and 50 common sunflower plants m−2, respectively. These results highlight the high level of weed control required in high-yielding cotton to ensure crop losses do not exceed the cost of control.

Crop plants have been used as mimic weeds to substitute for real weeds in competition studies. These mimic weeds have the advantages of availability of seed, uniform germination and growth, and the potential to confer better experimental controllability and repeatability. However, the underlying assumption that the competitive effects of mimic weeds are similar to real weeds has not been tested. We compared a range of morphological traits (plant height, node and leaf number, leaf area, leaf size, and dry weight) between the mimic weeds and real weeds: Japanese millet vs. junglerice, mungbean vs. bladder ketmia, and common sunflower vs. fierce thornapple. The impact of these mimic and real weeds on cotton was also assessed. There were similarities and differences between the mimic and real weeds, but impact on cotton lint yield was most closely associated with weed height and dry weight at mid-season. Mimic weeds may be satisfactorily substituted for real weeds in competition experiments where seasonal and environmental conditions are not limiting, such as with fully irrigated cotton, provided the plants have similar dry weight and height at mid-season. Alternatively, one can account for the differences in dry weight and height. We define here a generalized relationship estimating the yield loss of high-yielding, irrigated cotton from weed competition over a range of weed dry weights and heights, allowing extrapolation from the results with mimic weeds to the competitive effects of a range of weeds.

Coolatai grass is an invasive, perennial grass from Africa and the Middle East that has infested large areas of northern New South Wales, Australia, and also occurs in other Australian states. An understanding of the seed germination ecology of Coolatai grass can assist in predicting its potential distribution and developing effective management strategies. The effects of various environmental factors on Coolatai grass seed germination were investigated in a series of laboratory experiments. The effect of diurnal alternating temperatures (5–45 C) with a 12-h photoperiod were examined on a thermogradient plate. Seed germination occurred at almost all temperature combinations from 5 to 45 C. At moderate temperatures the speed of seed germination was very high; at 30/20 C more than 80% of seeds were germinated within 12 h. Germination was slightly enhanced by the presence of light, but length of photoperiod did not affect germination. Germination at neutral pH was over 90%, and declined to 65% at acidic (pH 4) and alkaline (pH 10) pH levels. Germination was completely inhibited at an osmotic stress of −0.55 MPa or greater and was reduced by 50% at −0.37 MPa. Greater germination in relatively dry soil conditions compared with native species may contribute to the establishment of this species in the field. Results indicate that Coolatai grass seeds can germinate over a wide range of diurnal temperatures, light regimes, pH levels, and under marginal water stress. These characteristics help explain the successful invasion of Coolatai grass and provide evidence that this species is capable of establishing in many parts of Australia.