The western Himalayan region in Pakistan has been shown to be the center of diversity of Puccinia striiformis; however, little is known about its genetic relations with the eastern part of the Himalayas. We studied the genetic structure of P. striiformis from Nepal (35 isolates) and Bhutan (31 isolates) in comparison with 81 Pakistani samples collected during 2015 and 2016, through microsatellite genotyping. Genetic analyses revealed a recombinant and highly diverse population structure in Pakistan, Bhutan, and Nepal. A high level of genotypic diversity (>0.90) was observed for the three countries of Pakistan (0.96), Bhutan (0.96), and Nepal (0.91) with the detection of 108 distinct multilocus genotypes (MLGs) in the overall population; 59 for Pakistan, 27 for Bhutan, and 26 for Nepal. Mean number of alleles per locus and gene diversity were higher in Nepal (3.19 and 0.458, respectively) than Bhutan (3.12 and 0.458, respectively). A nonsignificant difference between the observed and the expected heterozygosity in all populations further confirmed the recombinant structure. A clear population subdivision between the Himalayan region of Nepal, Bhutan, and Pakistan was evident, as revealed by F_ST values (ranging between 0.111 to 0.198), discriminant analysis of principal components, and resampling of MLGs. Limited gene flow could be present between Nepal and Bhutan, while the population from Pakistan was clearly distinct, and no divergence was present between two populations from Pakistan (Bajaur and Malakand). The overall high diversity and recombination signature suggested the potential role of recombination in the eastern Himalayan region (Nepal and Bhutan), which needs to be considered during host resistance deployment and in the context of aerial dispersal of the pathogen. Further surveillance should be made in the Himalayan region for disease management in the region and in the context of worldwide invasions. [ ] Copyright © 2019 The Author(s). This is an open access article distributed under the CC BY 4.0 International license .

Phosphorus (P) fertiliser is applied regularly to the nutrient-poor sandy soils in southwestern Australia to elevate and/or maintain pasture production. This study aimed to characterise differential growth, root carboxylate exudation, and mycorrhizal responses in three temperate perennial pasture grasses at variable P supply. Tall fescue (Festuca arundinacea L. cv. Prosper), veldt grass (Ehrharta calycina Sm. cv. Mission), and tall wheatgrass (Thinopyrum ponticum L. cv. Dundas) with five P rates varying from 0 to 100 mg P kg⁻¹ soil were evaluated in a controlled environment. Rhizosphere carboxylate exudation and mycorrhizal colonisation were assessed. Veldt grass produced the maximum shoot dry weight, highest agronomic phosphorus-use efficiency at low P supply, as well as the highest specific root length and shoot P content at all P rates. Across species, the maximum shoot weight was obtained at 20 and 50 mg P kg⁻¹ soil, which differed significantly from the two lowest P rates (0 and 5 mg P kg⁻¹ soil). Phosphorus application influenced carboxylate exudation, with plants exuding acetate only in the zero P treatment, and citrate and malonate in the P-supplemented treatments. In all three species, acetate and malonate were the major carboxylates exuded (37–51% of the total). Only tall wheatgrass released trans-aconitate. Citrate and malonate concentrations in the rhizosphere increased with P supply, suggesting their important role in P acquisition. Phosphorus applications reduced arbuscular mycorrhizal colonisation and increased root diameter as the P rate increased. Root carboxylate exudation in low-P soil played a role in mobilisation of P via P solubilisation, but the role of exuded carboxylate in soils well supplied with P might be diminished.