Propylea japonica (Coleoptera: Coccinellidae) is a natural enemy insect with a wide range of predation in Chinese mainland and is commonly used in pest management.  However, its genetic pattern (i.e., genetic variation, genetic structure, and historical population dynamics) is still unclear, impeding the development of biological control of insect pests.  Population genetic research has the potential to optimize strategies at different stages of the biological control processes.  This study used 23 nuclear microsatellite sites and mitochondrial COI genes to investigate the population genetics of Propylea japonica based on 462 specimens collected from 30 sampling sites in China.  The microsatellite dataset showed a moderate level of genetic diversity, but the mitochondrial genes showed a high level of genetic diversity.  Populations from the Yellow River basin were more genetically diverse than those in the Yangtze River basin.  Propylea japonica has not yet formed a significant genealogical structure in China, but there was a population structure signal to some extent, which may be caused by frequent gene flow between populations.  The species has experienced population expansion after a bottleneck, potentially thanks to the tri-trophic plant–insect–natural enemy relationship.  Knowledge of population genetics is of importance in using predators to control pests.  Our study complements existing knowledge of an important natural predator in agroecosystems through estimating its genetic diversity and population differentiation and speculating about historical dynamics.

Plastic film mulch in agricultural production becomes essential to maintaining crop yields in arid and semiarid areas. However, the presence of residual film in farmland soil has also drawn much attention. In this study, three experiments were conducted. The first two experimental designs included 0, 450, 1 350, and 2 700 kg ha–1 of residual film pieces of approximately 5 cm side length added to field soil (0–20 cm soil depth) for seven years and added to pots for four years. In the third experiment, 1 350 kg ha^–1 of the residual film with different side lengths (2–5, 5–10, 10–15, and 15–20 cm) was added to field soil for six years to explore the effect of residual film fragment size on soil nutrients, soil microorganisms, crop growth and yields. The residual film had little effect on the soil moisture at a field depth of 0–2 (or 0–1.8) m. There were no significant effects on organic carbon, total nitrogen, inorganic nitrogen, total phosphorus or available phosphorus in the 0–20 cm soil layer. The presence of residual film decreased the richness and diversity of the bacterial community of the surface soil of the residual film, but it had no significant effect on the microbial community of the non-surface soil. The emergence rates of wheat and lentils occasionally decreased significantly with different amounts of residue fragments added to the field. At 450–2 700 kg ha^–1, the residual film reduced the plant height and stem diameter of maize and significantly reduced the shoot biomass of harvested maize by 11–19%. The average yields of maize and potato over the seven years decreased, but there were almost no significant statistical differences among the treatments. These results provide important data for a comprehensive scientific understanding of the effects of residual film on soil and crops in dryland farming systems.

Chemicals that modify pest behavior are developed to reduce crop damage by altering pest behavior, using specific genes within the olfactory system as molecular targets. The identification of these molecular targets in Bactrocera dorsalis, also known as the functional study of key olfactory genes, relies on CRISPR/Cas9-mediated gene knockout techniques. However, these techniques face limitations when applied to lethal genes. Transgenic technology offers a solution since it enables precise manipulation of gene expression in specific tissues or during certain developmental stages. Consequently, this study developed a piggyBac-mediated transgenic system in B. dorsalis to investigate reporter gene expression in olfactory organs, and assessed the olfactory behavior and antennal electrophysiological responses in transgenic lines. The goal was to assess the potential of this approach for future research on olfactory gene function. A universally expressed housekeeping gene from the BdorActin family was identified using the developmental transcriptome dataset. Its candidate promoter region (BdorActinA3a-1^P-2k) was then cloned into the piggyBac plasmid. We subsequently established two stable transgenic lines with specific TTAA insertion sites on chromosomes 4 and 5, consistent with the characteristics of piggyBac transposition. The transgenic strains exhibited essentially normal survival, with hatchability and adult lifespan unaffected, although there were slight reductions in the emergence rate and oviposition capacity. The fluorescent reporter has been successfully expressed in olfactory-related organs, such as the antennae, proboscis, maxillary palp, legs, external genitalia, and brain. The antennal electrophysiological responses to representative chemicals in the transgenic lines were consistent with those of the wild type. However, some olfactory-related behaviors, such as pheromone response and mating, were significantly affected in the transgenic lines. These findings suggest that our system could potentially be applied in future olfactory research, such as driving the expression of exogenous elements that are effective in olfactory organs. However, caution is advised regarding its impact when applied to some olfactory-related behavioral phenotypes.