SummaryChina is the origin and evolutionary centre of Oriental pears. Pyrus betuleafolia is a wild species native to China and distributed in the northern region, and it is widely used as rootstock. Here, we report the de novo assembly of the genome of P. betuleafolia‐Shanxi Duli using an integrated strategy that combines PacBio sequencing, BioNano mapping and chromosome conformation capture (Hi‐C) sequencing. The genome assembly size was 532.7 Mb, with a contig N50 of 1.57 Mb. A total of 59 552 protein‐coding genes and 247.4 Mb of repetitive sequences were annotated for this genome. The expansion genes in P. betuleafolia were significantly enriched in secondary metabolism, which may account for the organism's considerable environmental adaptability. An alignment analysis of orthologous genes showed that fruit size, sugar metabolism and transport, and photosynthetic efficiency were positively selected in Oriental pear during domestication. A total of 573 nucleotide‐binding site (NBS)‐type resistance gene analogues (RGAs) were identified in the P. betuleafolia genome, 150 of which are TIR‐NBS‐LRR (TNL)‐type genes, which represented the greatest number of TNL‐type genes among the published Rosaceae genomes and explained the strong disease resistance of this wild species. The study of flavour metabolism‐related genes showed that the anthocyanidin reductase (ANR) metabolic pathway affected the astringency of pear fruit and that sorbitol transporter (SOT) transmembrane transport may be the main factor affecting the accumulation of soluble organic matter. This high‐quality P. betuleafolia genome provides a valuable resource for the utilization of wild pear in fundamental pear studies and breeding.

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Due to high volatility and water solubility, 2,4-dichlorophenoxyacetic acid (2,4-D) can easily enter into the atmosphere and water bodies by volatilization, drift, leaching, or runoff, which results in potential threats to the environment and human health. The physicochemical properties of pesticides can be regulated by preparing their ionic liquids. In this work, a series of dicationic ionic liquids (DILs) of 2,4-D were prepared to reduce its environmental risk and enhance herbicidal activity. The solubility, octanol-water partition coefficient, surface tension, and volatilization rate results of DILs showed that these properties could be optimized by choosing appropriate countercations. Compared to 2,4-D ammonium salt, DILs have lower volatility, water solubility, and surface tension as well as higher lipophilicity. Benefiting from optimized physicochemical properties, DILs HIL8-12 exhibited better herbicidal activity against three typical broadleaf weeds than 2,4-D ammonium salt, and their fresh weight inhibition rates increased by 2.74-46.84%. The safety assessment experiment indicated that DILs were safer to wheat than commercialized forms of 2,4-D. The DILs could reduce the environmental risk of 2,4-D caused by high volatility and water solubility and would be potential alternatives to its commercialized formulations.

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