KAR(1) responses are more complex than simply stating whether a species is responsive or non-responsive; light and temperature conditions, dormancy state and seed lot all influence the sensitivity of seeds to KAR(1), and a response to KAR(1) can be induced. Three response types for generalizing KAR(1) responses are proposed, namely inherent, inducible and undetected. Given that responses to KAR(1) were either inherent or inducible in all 15 seed lots included in this study, the Brassicaceae may be an ideal target for future application of KAR(1) in weed management.

The smoke-derived chemical karrikinolide commonly triggers seeds in the Brassicaceae, Solanaceae and Asteraceae families to germinate, yet species in the Poaceae – another major understorey and weed family – have responded to the chemical with mixed results. This study aimed to understand why some grass species respond to karrikinolide while others do not. Using a field-based seed-burial trial, dose-response experiment, and stratification experiment, we investigated whether karrikinolide could alleviate dormancy and trigger seeds to germinate for seven global agronomic weeds: Avena fatua L., Lolium rigidum Gaudin, Eragrostis curvula (Schrad.) Nees, Phalaris minor Retz., Hordeum glaucum Steud., Ehrharta calycina Sm. and Bromus diandrus Roth. Seeds of A. fatua were consistently stimulated to germinate with karrikinolide in all experiments, whether seeds were freshly collected or dormancy had been partially alleviated. In contrast, seeds of L. rigidum failed to respond to karrikinolide when the seeds were fresh, after-ripened in the laboratory, and even during natural dormancy loss in the field. Interestingly, although karrikinolide did not stimulate freshly collected E. curvula seeds to germinate, it hastened dormancy loss when applied during stratification. These findings are helpful for understanding the responses of grass species following fire. They also contribute to a growing body of research aimed at using karrikinolide as a tool for triggering uniform germination of seeds for enhancing restoration efforts and depleting the weed seed bank.

Seed water content and history of imbibition were found to significantly influence whether seeds germinate in response to KAR(1). To optimize the germination response of seeds, KAR(1) should be applied to dry seeds, when sensitivity to ABA is minimized.

Limited success of restoring framework banksia-woodland species has been attributed to the failure of seedlings to establish deep root systems before the onset of the summer drought. The present glasshouse study investigated how optimising nutrient application during nursery production may increase new-root production after outplanting. Two experimental streams were established to (1) optimise nutrient application rates during nursery production and (2) utilise nutrient-loading techniques to improve root production of Banksia menziesii R.Br., Banksia attenuata R.Br. and Eucalyptus todtiana F.Muell after outplanting. Optimal nutrient-application rates were determined by measuring plant growth and internal nutrient responses to eight application levels of slow-release fertiliser (0–18 kg m–3, nitrogen (N) : phosphorus (P) : potassium (K) = 17 : 1.6 : 8.7). Nutrient-loading treatments utilised seedlings that had been grown under common industry fertiliser conditions (3 kg m–3 native Osmocote, N : P : K = 17 : 1.6 : 8.7) supplied with ‘low’ or ‘high’ loading doses of liquid Thrive continuously over 6 weeks, immediately before outplanting. Seedlings from both experiments were then outplanted to 1-m-deep poly-pipe tubes containing habitat soil. After 12 weeks, plants were harvested and new-root production and shoot growth were measured. Optimal concentrations of slow-release fertiliser for maximum outplanting success as indicated by increased root investment (root : shoot ratio and new-root production) were 8–12 kg m–3 for all species. Nutrient loading increased N and P concentrations of plants by up to 80% and 127%, respectively, by luxury nutrient consumption, and after planting, nutrient-loaded seedlings produced 1.5-fold the biomass of conventionally fertilised seedlings, this being the result of greater root productivity. In conclusion, optimising nursery nutrient regimes for framework species may increase root-growth potential, assisting in improving plant establishment in restoration programs.