Abstract
As a result of global climate change, insects are increasingly being exposed to extreme temperature events; yet population-level variation in heat tolerance and its underlying mechanisms remain poorly understood. In this study, we investigated thermal adaptation in four geographically distinct populations of the invasive mealybug Dysmicoccus neobrevipes from southern China. The populations were subjected to acute heat stress across a gradient of temperatures where survival, fecundity, offspring viability, and sex ratio were quantified. We found pronounced geographic divergence in upper thermal limits: populations from warmer regions (Guangdong and Hainan) exhibited better survival, more stable reproductive output, and greater tolerance in offspring compared with populations from cooler regions (Guangxi and Yunnan). Thermal responses followed a nonlinear pattern, with moderate heat often enhancing performance, while temperatures above physiological thresholds triggered abrupt declines. Under heat stress, life-history strategies differed among populations, with some exhibiting stress-induced reproductive investment and others showing vulnerability across all traits. Importantly, acute heat exposure produced cross-generational effects, highlighting that parental thermal history can influence offspring performance. These results demonstrate that population-specific climatic adaptation, nonlinear physiological limits, and life-history trade-offs jointly shape thermal tolerance. Understanding these mechanisms provides a predictive framework for anticipating invasive pest expansion under future climatic warming and informs region-specific pest management strategy development.