The frequency and amplitude of heat waves are predicted to increase under future climate change conditions. We still lack a detailed understanding of how changes in the frequency and amplitude of heat waves are linked to the life history traits and biocontrol efficiency of host-feeding parasitoids. In the present study, we simulated a series of heat waves as a function of amplitude and frequency to investigate the effects on the life history traits of the host-feeding parasitoid Eretmocerus hayati. We found that both the amplitude and frequency of heat waves significantly affected the adult phenotypes. In the low-amplitude heat wave group, the frequency of heat waves did not change the life history traits of the parasitoid; however, when the heat amplitude reached 42 °C, medium (four times/week) and high frequencies (seven times/week) of heat waves detrimentally affected these parameters. Hence, these findings suggest that to obtain optimal biological control with this parasitoid, we need to carefully monitor heat wave pattern (especially the amplitude and frequency) over the short term (usually 7–10 days) before releasing a host-feeding parasitoid.

Tuta absoluta is one of the most significant invasive pests affecting tomato plants worldwide. RT-qPCR has emerged as one of the most sensitive and accurate methods for detecting gene expression data. The screening of stable internal reference genes is the most critical step for studying the molecular mechanisms of environmental adaptability. The stable reference genes expressed in T. absoluta under specific experimental conditions have not yet been clarified. In this study, seven candidate reference genes (RPL27, RPS13, RPS15, EF1-α, TUB, TBP, and β-actin) and their optimal numbers were evaluated under biotic (developmental stages and adult tissues) and abiotic (insecticide, temperature, and plant VOC) conditions using four software programs. Our results identified the following reference genes and numbers as optimal: three genes (EF1-α, RPS13, and RPL27) for different developmental stages (egg, larva, pupa, unmated adult), two genes (RPS13 and TBP) for adult tissues (antenna, head, thorax, abdomen, leg), two genes (TBP and RPS13) for insecticides (Bacillus thuringiensis, chlorpyrifos, abamectin-aminomethyl, and chlorantraniliprole), two genes (RPL27 and TUB) for temperature-induced stresses (0, 25, and 40 °C), and two genes (RPS13 and TUB) for VOC-induced stresses (nonanal, α-phellandrene, and tomato leaves). Our results provide a reference for selecting appropriate reference genes for further study of the functional genes of T. absoluta under different experimental conditions.

Anastomosis groups (AGs) or subgroups of 244 Rhizoctonia isolates recovered from sugar beet roots with symptoms of root and crown rot were characterized to be AG-A, AG-K, AG-2-2IIIB, AG-2-2IV, AG-3 PT, AG-4HGI, AG-4HGII, and AG-4HGIII, with AG-4HGI (108 isolates, 44.26%) and AG-2-2IIIB (107 isolates, 43.85%) being predominate. Four unclassified mycoviruses and one hundred and one putative mycoviruses belonging to six families, namely Mitoviridae (60.00%), Narnaviridae (18.10%), Partitiviridae (7.62%), Benyviridae (4.76%), Hypoviridae (3.81%), and Botourmiaviridae (1.90%), were found to be present in these 244 Rhizoctonia isolates, most of which (88.57%) contained positive single-stranded RNA genome. The 244 Rhizoctonia isolates were all sensitive to flutolanil and thifluzamide, with average median effective concentration (EC₅₀) value of 0.3199 ± 0.0149 μg·mL⁻¹ and 0.1081 ± 0.0044 μg·mL⁻¹, respectively. Among the 244 isolates, except for 20 Rhizoctonia isolates (seven isolates of AG-A and AG-K, one isolate of AG-4HGI, and 12 isolates of AG-4HGII), 117 isolates of AG-2-2IIIB, AG-2-2IV, AG-3 PT, and AG-4HGIII, 107 isolates of AG-4HGI, and six isolates of AG-4HGII were sensitive to pencycuron, with average EC₅₀ value of 0.0339 ± 0.0012 μg·mL⁻¹. Correlation index (ρ) of cross-resistance level between flutolanil and thifluzamide, flutolanil and pencycuron, and thifluzamide and pencycuron was 0.398, 0.315, and 0.125, respectively. This is the first detailed study on AG identification, mycovirome analysis, and sensitivity to flutolanil, thifluzamide, and pencycuron of Rhizoctonia isolates associated with sugar beet root and crown rot.

The clover cutworm, Scotogramma trifolii Rottemberg (Lepidoptera: Noctuidae), is a globally distributed polyphagous pest causing significant economic losses to agricultural crops. RT-qPCR is a gold-standard technique for gene expression analysis, yet its accuracy depends critically on stable reference genes for data normalization. To address the lack of validated reference genes in S. trifolii, we evaluated six candidate genes (β-actin, RPL9, GAPDH, RPL10, EF1-α, and TUB) across four developmental stages (egg, larva, pupa, and adult) and six adult tissues (head, thorax, abdomen, wings, legs, and antennae) using geNorm, NormFinder, BestKeeper, and RefFinder algorithms. Stability analysis identified β-actin, RPL9, and GAPDH as the most reliable reference genes for developmental stage normalization, while RPL10, GAPDH, and TUB were validated for adult tissues. Functional validation using the odorant receptor gene StriOR20 revealed significant discrepancies in relative expression levels when normalized with unstable reference genes (TUB and RPL9), emphasizing the necessity of rigorous reference gene selection. This study establishes the first comprehensive reference gene panel for S. trifolii, providing a robust foundation for gene expression studies in this agriculturally important pest.

Rhizoctonia solani anastomosis group (AG)-2-2IIIB and AG-4HGI are the main pathogens causing sugar beet seedling damping-off and crown and root rot disease. In this study, 1232 loci of simple sequence repeats (SSRs) were obtained via transcriptome sequencing, with 592 from AG-2-2IIIB and 640 from AG-4HGI. Fourteen and twenty loci of SSRs were selected for studying the genetic structure of the AG-2-2IIIB and AG-4HGI populations, respectively. A population of 134 strains of AG-2-2IIIB and 145 strains of AG-4HGI, sampled from three geographic regions in China, indicated that both AG-2-2IIIB and AG-4HGI had a high level of genetic diversity, and that the selected SSR markers could reliably capture the genetic variation. Genetic analysis indicated that the individual strains of AG-2-2IIIB and AG-4HGI randomly mated within their respective population, and that a considerable degree of inbreeding was present among the populations. High to moderate gene flow and low to moderate population subdivision were detected among the populations of AG-2-2IIIB and AG-4HGI, which indicated that weak differentiation existed in these two subgroups. In addition, a founder effect (genetic drift) or a bottleneck effect was inferred to have occurred in the AG-4HGI population. This study provides the first analysis of the population genetic structure of AG-2-2IIIB and AG-4HGI associated with sugar beet seedling damping-off and crown and root rot disease, and the present results offer useful guidance for developing effective integrated disease management.