Summary Harnessing plant microbiota can assist in sustainably increasing primary productivity to meet growing global demands for food and biofuel. However, development of rational microbiome‐based approaches for improving crop yield and productivity is currently hindered by a lack of understanding of the major biotic and abiotic factors shaping the crop microbiome under relevant field conditions. We examined bacterial and fungal communities associated with both aerial (leaves, stalks) and belowground (roots, soil) compartments of four commercial sugarcane varieties (Saccharum spp.) grown in several growing regions in Australia. We identified drivers of the sugarcane microbiome under field conditions and evaluated whether the plants shared a core microbiome. Sugarcane‐associated microbial assemblages were primarily determined by plant compartment, followed by growing region, crop age, variety and Yellow Canopy Syndrome (YCS). We detected a core set of microbiota and identified members of the core microbiome that were influenced by YCS incidence. Our study revealed key hub microorganisms in the core microbiome networks of sugarcane leaves, stalks, roots and rhizosphere soil despite location and time‐associated shifts in the community assemblages. Elucidating their functional roles and identification of the keystone core microbiota that sustain plant health could provide a technological breakthrough for a sustainable increase in crop productivity.

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A greenhouse hydroponic experiment was performed using salt-tolerant (cv. Suntop) and -sensitive (Sunmate) wheat cultivars and a salt-tolerant barley cv. CM72 to evaluate how cultivar and species differ in response to salinity stress. Results showed that wheat cv. Suntop performed high tolerance to salinity, being similar tolerance to salinity with CM72, compared with cv. Sunmate. Similar to CM72, Suntop recorded less salinity induced increase in malondialdehyde (MDA) accumulation and less reduction in plant height, net photosynthetic rate (Pn), chlorophyll content, and biomass than in sensitive wheat cv. Sunmate. Significant time-course and cultivar-dependent changes were observed in the activities of antioxidant enzymes such as superoxide dismutase (SOD), peroxidase (POD), catalase (CAT), ascorbate peroxidase (APX), and glutathione reductase (GR) in roots and leaves after salinity treatment. Higher activities were found in CM72 and Suntop compared to Sunmate. Furthermore, a clear modification was observed in leaf and root ultrastructure after NaCl treatment with more obvious changes in the sensitive wheat cv. Sunmate, rather than in CM72 and Suntop. Although differences were observed between CM72 and Suntop in the growth and biochemical traits assessed and modified by salt stress, the differences were negligible in comparison with the general response to the salt stress of sensitive wheat cv. Sunmate. In addition, salinity stress induced an increase in the Na+ and Na+/K+ ratio but a reduction in K+ concentrations, most prominently in Sunmate and followed by Suntop and CM72.

Diaphorina citri Kuwayama (Hemiptera: Sternorrhyncha: Psyllidae) is a vector of huanglongbing, a disease of citrus that in Asia is caused by ‘Candidatus Liberibacter asiaticus’ (α‐Proteobacteria) (Las). Acquisition of Las by D. citri appears to be variable, and this variability may be due to the suitability of the host plants and their tissues for acquisition. Therefore, this study aimed to determine the effect of symptom severity of the disease on the feeding behaviour of D. citri. Use of an electrical penetration graph showed that the pathway phase of D. citri consisted of four waveforms, A, B, C, and D; waveforms A and B have not been reported for D. citri before. The remaining waveforms, E1, E2, and G, conform to those described before for D. citri. The duration of the non‐penetration period did not differ between healthy or infected plants. However, in moderately and severely symptomatic plants, the duration of the pathway phase increased, whereas the phloem phase was shorter. In all diseased plants, the times to first and sustained salivation in the phloem were longer than those in control plants, with the times being related to symptom severity. As symptom expression increased, the percentage of time spent by psyllids salivating during the phloem phase increased; however, the percentage of time spent in phloem activities reduced gradually from ca. 74% in the control plants to ca. 8% in the severely symptomatic plants. In contrast, the percentage of time spent on xylem activities increased, as did the proportion of psyllids feeding from xylem. The differences in the durations of the E waveforms on plants showing different levels of symptom expression may account for differences in acquisition found amongst studies; therefore, future work on the acquisition and transmission of Las needs to carefully document symptom expression.

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