Plastic adjustments of physiological tolerance to a particular stressor can result in fitness benefits for resistance that might manifest not only in that same environment but also be advantageous when faced with alternative environmental stressors, a phenomenon termed 'cross-tolerance'. The nature and magnitude of cross-tolerance responses can provide important insights into the underlying genetic architecture, potential constraints on or versatility of an organism's stress responses. In this study, we tested for cross-tolerance to a suite of abiotic factors that likely contribute to setting insect population dynamics and geographic range limits: heat, cold, desiccation and starvation resistance in adult Ceratitis rosa following acclimation to all these isolated individual conditions prior to stress assays. Traits of stress resistance scored included critical thermal (activity) limits, chill coma recovery time (CCRT), heat knockdown time (HKDT), desiccation and starvation resistance. In agreement with other studies, we found that acclimation to one stress typically increased resistance for that same stress experienced later in life. A more novel outcome, however, is that here we also found substantial evidence for cross-tolerance. For example, we found an improvement in heat tolerance (critical thermal maxima, CT max ) following starvation or desiccation hardening and improved desiccation resistance following cold acclimation, indicating pronounced cross-tolerance to these environmental stressors for the traits examined. We also found that two different traits of the same stress resistance differed in their responsiveness to the same stress conditions (e.g. HKDT was less cross-resistant than CT max ). The results of this study have two major implications that are of broader importance: (i) that these traits likely co-evolved to cope with diverse or simultaneous stressors, and (ii) that a set of common underlying physiological mechanisms might exist between apparently divergent stress responses in this species. This species may prove to be a valuable model for future work on the evolutionary and mechanistic basis of cross-tolerance.

Although reports have documented loss of species diversity and ecological services caused by stressful temperature changes that result from climate change, some species cope through behavioral compensation. As temperatures and magnitudes of temperature extremes increase, animals should compensate to maintain fitness (such as through temporary behavioral shifts in activity times). Appropriate timing of activity helps avoid competition across species. Although coprophagic dung beetles exhibit species-specific temporal activity times, it is unknown whether temperature drives evolution of these species-specific temporal activity times. Using nine dung beetle species (three each of diurnal, crepuscular, and nocturnal species), we explored differences in heat stress tolerance measured as critical thermal maxima (CT max ; the highest temperature allowing activity) and heat knockdown time (HKDT; survival time under acute heat stress) across these species, and examined the results using a phylogenetically informed approach. Our results showed that day-active species had significantly higher CT max (diurnal > crepuscular = nocturnal species), whereas crepuscular species had higher HKDT (crepuscular > nocturnal > diurnal species). There was no correlation between heat tolerance and body size across species with distinct temporal activity, and no significant phylogenetic constraint for activity. Species with higher CT max did not necessarily have higher HKDT, which indicates that species may respond differently to diverse heat tolerance metrics. Acute heat tolerance for diurnal beetles indicates that this trait may constrain activity time and, under high acute temperatures with climate change, species may shift activity times in more benign environments. These results contribute to elucidate the evolution of foraging behavior and management of coprophagic beetle ecosystem services under changing environments.

Since the first detection of Bactrocera dorsalis in Botswana in 2010, the establishment, spread, and response to prevailing Botswana microclimates under rapidly changing environments remain unknown. This study investigated the presence, seasonal population abundance, and thermal biology of B. dorsalis in Botswana. We measured B. dorsalis thermal tolerance vis critical thermal limits (CTLs) and lethal temperature assays (LTAs) to understand how temperature largely impacts on fitness and hence invasive potential. Seasonal monitoring results indicated B. dorsalis establishment in the Chobe district (its first area of detection). Trap catches showed continuous adult flies’ presence all year round and high average monthly trap catches as compared with other districts. Furthermore, B. dorsalis was detected south of Botswana, including Kgatleng, Kweneng, South-east, and Southern districts. Critical thermal maxima (CTmax) to activity for adults and larvae were 46.16°C and 45.23°C, whereas critical thermal minima (CTmin) to activity for adults and larvae were 9.1°C and 7.3°C, respectively. Moreover, we found an improved CTmin for larvae at a slower ramping rate, indicating potential rapid cold hardening. The lower lethal temperature (LLT) and upper lethal temperature (ULT) assays revealed a reduction in survival at all the developmental stages as severity and duration of both temperature extremes increased. Microclimatic temperatures recorded in Botswana showed that environmental temperatures fall within the thermal breath of B. dorsalis activity measured here, indicating a potential conducive climate niche for the insect pest across the country, albeit other factors, e.g., host availability, play a significant role. These results therefore suggest that Botswana microclimatic temperatures aided B. dorsalis activity and invasion pathway are thus significant in mapping invasions and pest risk analysis, and may also aid in designing pest management strategies.

1. Low temperatures affect insect functioning and population dynamics. Although temperate species cope with low temperatures better than their tropical counterparts, increasing temperature variability due to climate change exposes tropical species to frequent cold stress. For keystone insect species providing important ecosystem services, low-temperature tolerances, and behavioural responses remain unknown, hampering predictions under climate change.2. The present study examined low-temperature physiology [critical thermal minima (CT min ) and chill coma recovery time (CCRT)] of six dung beetle species across three activity times: diurnal Allogymnopleurus indigaceous (Reiche) and Euoniticellus intermedius (Reiche); crepuscular Onthophagus alexis (Klug) and Onthophagus gazella (Fabricius), and; nocturnal Copris elephenor (Klug) and Scarabaeus zambezianus (Peringuey). Further, ecological service delivery (dung removal) was examined between diurnal and nocturnal species across the temperature regimes.3. Nocturnal species had significantly greater cold tolerance than both crepuscular and diurnal species, while CCRT was significantly shortest in diurnal than both crepuscular and nocturnal species. Dung ball production between diurnal and nocturnal species interacted with temperature, with diurnal species producing significantly fewer balls at low temperatures, while nocturnal beetles were not significantly affected. In turn, nocturnal species produced significantly larger balls than the diurnal species across temperatures. Effects of temperature regime shifts were intertwined with the foraging ecology of individual species.4. Future research should quantify species' functional responses toward different amounts of dung masses as stressful temperatures increase.5. Results are significant for determination of species thermal ranges and predicting costs of low-temperature stress through reduced ecological services under shifting thermal environments.

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