Search

Fluctuating Thermal Regimes (FTR), where organisms are held at low temperatures with a brief, daily warm pulse, have been shown to increase longevity in adult insects and improve pupa survival while reducing sublethal effects. We used FTR to extend the longevity and thus generation time of the fly species Themira biloba (Diptera: Sepsidae). T. biloba can be maintained in continuous culture and requires an insecticide-free dung substrate for larval growth and development. Our objective was to decrease labor and consumable materials required to maintain insect species in critical scientific collections using FTR. We extended pupation time from 4 days up to 8 weeks with no increase in mortality, and mean adult longevity was increased from 12 days to 50 days. FTR is a valuable tool for reducing the investment required to maintain rare and exotic insects., (Published by Elsevier Ltd.)

The adaptability of organisms to novel environmental conditions depends on the amount of genetic variance present in the population as well as on the ability of individuals to adjust their phenotype through phenotypic plasticity. Here, we investigated the phenotypic plasticity induced by a single generation's exposure to three different temperature regimes with respect to several life-history and stress-resistance traits in a natural population of Drosophila simulans. We studied a constant as well as a predictably and an unpredictably fluctuating temperature regime. We found high levels of phenotypic plasticity among all temperature regimes, suggesting a strong influence of both temperature fluctuations and their predictability. Increased heat tolerance was observed for flies developed in both types of fluctuating thermal environments compared with flies developed in a constant environment. We suggest that this was due to beneficial hardening when developing in either fluctuating temperature environment. To our surprise, flies that developed in constant and predictably changing environments were similar to each other in most traits when compared to flies from the unpredictably fluctuating environment. The unpredictably changing thermal environment imposed the most stressful condition, resulting in the lowest performance for stress-related traits, even though the absolute temperature changes never exceeded that of the predictably fluctuating environment. The overall decreased stress resistance of flies in the unpredictably fluctuating environment may be the consequence of maladaptive phenotypic plasticity in this setting, indicating that the adaptive value of plasticity depends on the predictability of the environment., (© 2014 European Society For Evolutionary Biology. Journal of Evolutionary Biology © 2014 European Society For Evolutionary Biology.)

This study aimed to evaluate the effectiveness of A. oryzae in inhibiting aflatoxin B1 (AFB1) and ochratoxin A (OTA) production by A. flavus and A. carbonarius, respectively, under shifting temperatures. A. oryzae was tested on different agar, namely coconut cream agar (CCA) and chili-based agar to figure out the variation in the effectiveness of A. oryzae on the most appropriate medium for A. flavus and A. carbonarius to produce mycotoxin and under natural condition where they are predominantly found. On CCA, the temperatures applied were 20, 30, 35, 40, 20/30, 20/35, and 20/40 °C, while on chili-based agar, the temperatures imposed were 20, 40, and 20/40 °C, at varied water activity of 0.92 and 0.97aw. The findings indicated that A. oryzae was much more effective in inhibiting the growth of A. flavus rather than A. carbonarius, yet it was able to inhibit higher OTA concentration than AFB1 at fluctuating temperatures on CCA as the most appropriate medium for A. flavus and A. carbonarius. A. oryzae effectively inhibited AFB1 and OTA at static temperature of 20 °C and water activity of 0.97aw on chili-based agar. Under fluctuating temperatures (20/40 °C), A. oryzae was also able to control mycotoxin, particularly OTA at high water activity (0.97aw). [ABSTRACT FROM AUTHOR]

Environmental temperature is a crucial abiotic factor that influences the success of ectothermic organisms, including hosts and pathogens in disease systems. One example is the amphibian chytrid fungus, Batrachochytrium dendrobatidis (Bd), which has led to widespread amphibian population declines. Understanding its thermal ecology is essential to effectively predict outbreaks. Studies that examine the impact of temperature on hosts and pathogens often do so in controlled constant temperatures. Although varying temperature experiments are becoming increasingly common, it is unrealistic to test every temperature scenario. Thus, reliable methods that use constant temperature data to predict performance in varying temperatures are needed. In this study, we tested whether we could accurately predict Bd growth in three varying temperature regimes, using a Bayesian hierarchical model fit with constant temperature Bd growth data. We fit the Bayesian hierarchical model five times, each time changing the thermal performance curve (TPC) used to constrain the logistic growth rate to determine how TPCs influence the predictions. We then validated the model predictions using Bd growth data collected from the three tested varying temperature regimes. Although all TPCs overpredicted Bd growth in the varying temperature regimes, some functional forms performed better than others. Varying temperature impacts on disease systems are still not well understood and improving our understanding and methodologies to predict these effects could provide insights into disease systems and help conservation efforts. [ABSTRACT FROM AUTHOR]

Diurnal fluctuations in temperature are ubiquitous in terrestrial environments, and insects and other ectotherms have evolved to tolerate or acclimate to such fluctuations. Few studies have examined whether ectotherms acclimate to diurnal temperature fluctuations, or how natural and domesticated populations differ in their responses to diurnal fluctuations. We examine how diurnally fluctuating temperatures during development affect growth, acclimation, and stress responses for two populations of Manduca sexta: a field population that typically experiences wide variation in mean and fluctuations in temperature, and a laboratory population that has been domesticated in nearly constant temperatures for more than 300 generations. Laboratory experiments showed that diurnal fluctuations throughout larval development reduced pupal mass for the laboratory but not the field population. The differing effects of diurnal fluctuations were greatest at higher mean temperature (30°C): Here diurnal fluctuations reduced pupal mass and increased pupal development time for the laboratory population, but had little effect for the field population. We also evaluated how mean and fluctuations in temperature during early larval development affected growth rate during the final larval instar as a function of test temperature. At an intermediate (25°C) mean temperature, both the laboratory and field population showed a positive acclimation response to diurnal fluctuations, in which subsequent growth rate was significantly higher at most test temperatures. In contrast at higher mean temperature (30°C), diurnal fluctuations significantly reduced subsequent growth rate at most test temperatures for the laboratory population, but not for the field population. These results suggest that during domestication in constant temperatures, the laboratory population has lost the capacity to tolerate or acclimate to high and fluctuating temperatures. Population differences in acclimation capacity in response to temperature fluctuations have not been previously demonstrated, but they may be important for understanding the evolution of reaction norms and performance curves. [ABSTRACT FROM AUTHOR]

Ecotoxicological studies considerably improved realism by assessing the toxicity of pollutants at different temperatures. Nevertheless, they may miss key interaction patterns between pollutants and temperature by typically considering only part of the natural thermal gradient experienced by species and ignoring daily temperature fluctuations (DTF). We therefore tested in a common garden laboratory experiment the effects of the pesticide chlorpyrifos across a range of mean temperatures and DTF on physiological traits (related to oxidative stress and bioenergetics) in low- and high-latitude populations of Ischnura elegans damselfly larvae. As expected, the impact of chlorpyrifos varied along the wide range of mean temperatures (12–34 °C). None of the physiological traits (except the superoxide anion levels) were affected by chlorpyrifos at the intermediate mean temperatures (20–24 °C). Instead, most of them were negatively affected by chlorpyrifos (reduced activity levels of the antioxidant defense enzymes superoxide dismutase [SOD], catalase [CAT] and peroxidase [PER], and a reduced energy budget) at the very high (≥28 °C) or extreme high temperatures (≥32 °C), and to lesser extent at the lower mean temperatures (≤16 °C). Notably, at the lower mean temperatures the negative impact of chlorpyrifos was often only present or stronger under DTF. Although the chlorpyrifos effects on the physiological traits greatly depended on the experimentally imposed thermal gradient, patterns were mainly consistent across the natural latitude-associated thermal gradient, indicating the generality of our results. The thermal patterns in chlorpyrifos-induced physiological responses contributed to the observed toxicity patterns in life history (reduced survival and growth at low and high mean temperatures). Taken together, our results underscore the importance of evaluating pesticide toxicity along a temperature gradient and of taking a mechanistic approach with a focus on physiology, to improve our understanding of the combined effects of pollutants and temperature in natural populations. [Display omitted] • Chlorpyrifos effects on physiology varied along a wide range of temperatures. • Chlorpyrifos had adverse effects at low and especially at high mean temperatures. • However, at intermediate temperatures, chlorpyrifos did not affect the physiology. • Patterns in physiological traits were strongly correlated with life history traits. [ABSTRACT FROM AUTHOR]

Temperature is a key factor affecting both dormancy and germination. In non-dormant seeds, when temperature is within the thermal range permissive for germination, it just regulates germination velocity, while in seeds presenting dormancy it can also be affecting dormancy level, dormancy termination and the expression of dormancy itself. This dual effect of temperature on dormancy and germination often leads to misinterpretation of obtained germination results and confounds the analysis of temperature effects in seed populations presenting some degree of dormancy. In the present paper we discuss the effect of temperature in the regulation of dormancy level and its implications in dormancy expression, as an attempt to construct a conceptual framework that allows distinguishing between the effects of temperature on dormancy and germination. Finally, we present examples of how a better understanding of these effects could help us to interpret the mixed effects of temperature on both processes during incubation of seeds presenting dormancy. [ABSTRACT FROM AUTHOR]

An increasing intensity of stress is expected to affect the fitness traits of an organism more and more negatively, but in particular cases, extremely resistant individuals have been observed. The present study was undertaken to determine the effects of different stress intensities on fitness traits of the parasitoid wasp Aphidius ervi Haliday., We exposed 1-day-old mummies (dead aphids containing the parasitoid pupa) for 4 weeks to combinations of two low temperatures (4 and 0 °C, 0 °C being the most stressful) and two thermal regimes (constant and fluctuating, constant being the most stressful), representing four stress levels., The present results showed that resistant individuals occurred only in the most stressful treatment (0 °C, constant temperature), which induced a higher mortality rate. These resistant individuals performed almost as well as those of the control, but showed a reduction in their size. The fluctuating regimes, at both temperatures, presented a high emergence rate, but at the expense of higher lipid consumption. Unexpectedly, the fluctuating regime associated with the presumably more stressful temperature (0 °C) produced individuals without any decrease in the measured fitness traits, in contrast to the treatment expected to be less stressful (4 °C, fluctuating temperature)., This result opens a new area of research in stress ecology and could modify the practice of cold storage in biological control. [ABSTRACT FROM AUTHOR]

[Display omitted] • Temperature fluctuations affect the biology and cold tolerance of insects. • We tested the effects of temperature changes on the survival of SWD. • At mild temperatures (5 °C), increasing warm-up frequency was harmful. • At freezing temperatures (0 °C), daily warm-ups improved survival outcomes. • Fluctuating temperatures during cold acclimation similarly improved survival. • We conclude temperature fluctuations may affect overwintering survival of SWD. Among overwintering Drosophila suzukii , discrete environmental changes in temperature and photoperiod induce a suite of biochemical changes conferring cold tolerance. However, little is known regarding how temperature fluctuations, which can influence metabolic and cellular repair activity, affect survival outcomes in this species. For that reason, we designed three experiments to test the effects of intermittent warm-up periods and the degree of temperature fluctuation on winter-morphotype (WM) D. suzukii survival. We found that at 5 °C, a temperature sufficient to induce reproductive diapause, but warm enough to allow foraging, increasing warm-up frequency (warmed to 25 °C at various interval schedules) was associated with decreased survival. In contrast, when the nightly low temperature was 0 °C, daily fluctuations that warmed the environment to temperatures above freezing (5, or 15 °C) appeared beneficial and resulted in improved survival compared to flies held at 0 °C during day and night. When we next evaluated cold tolerance using a 24-hour stress test assay (-5 °C), we found that again, thermal fluctuations improved survival compared to static freezing conditions. However, we also found that WM D. suzukii exposed to freezing temperatures during acclimation were less cold tolerant, regardless of the thermal fluctuation schedule, indicating that there may be tradeoffs between adequate acclimation temperature, which is required to induce cold tolerance, and the ensuing effects of incidental chill injury. Moving forward, these data, which account for the nuanced interactions between the thermal environment and in the internal physiology of D. suzukii , may help refine seasonal populations models, which aim to forecast pest pressure based on conditions the previous winter. [ABSTRACT FROM AUTHOR]

Much interest exists in the extent to which constant versus fluctuating temperatures affect thermal performance traits and their phenotypic plasticity. Theory suggests that effects should vary with temperature, being especially pronounced at more extreme low (because of thermal respite) and high (because of Jensen's inequality) temperatures. Here we tested this idea by examining the effects of constant temperatures (10 to 30 °C in 5 °C increments) and fluctuating temperatures (means equal to the constant temperatures, but with fluctuations of ±5 °C) temperatures on the adult (F2) phenotypic plasticity of three thermal performance traits – critical thermal minimum (CT min), critical thermal maximum (CT max), and upper lethal temperature (ULT 50) in ten species of springtails (Collembola) from three families (Isotomidae 7 spp.; Entomobryidae 2 spp.; Onychiuridae 1 sp.). The lowest mean CT min value recorded here was -3.56 ± 1.0 °C for Paristoma notabilis and the highest mean CT max was 43.1 ± 0.8 °C for Hemisotoma thermophila. The Acclimation Response Ratio for CT min was on average 0.12 °C/°C (range: 0.04 to 0.21 °C/°C), but was much lower for CT max (mean: 0.017 °C/°C, range: -0.015 to 0.047 °C/°C) and lower also for ULT 50 (mean: 0.05 °C/°C, range: -0.007 to 0.14 °C/°C). Fluctuating versus constant temperatures typically had little effect on adult phenotypic plasticity, with effect sizes either no different from zero, or inconsistent in the direction of difference. Previous work assessing adult phenotypic plasticity of these thermal performance traits across a range of constant temperatures can thus be applied to a broader range of circumstances in springtails. • Adult springtails exhibit similar thermal tolerance plasticity when exposed to constant versus fluctuating temperatures. • Thermal tolerance trait values increase as acclimation temperature increases. • Previous work using constant temperatures to estimate critical thermal limits can be considered reliable. [ABSTRACT FROM AUTHOR]

Necrophagous fly species are commonly used as forensic tools to estimate the minimum postmortem interval (PMImin). Many researchers raised necrophagous flies under constant temperature regimes to collect their developmental data. However, in most forensic cases, the ambient temperature fluctuates. In order to investigate a forensically important fly developmental mode (the Isomegalen diagram, Isomorphen diagram and Thermal summation models) and make comparisons of the developmental rate between constant temperatures and fluctuating temperatures, we used Aldrichina grahami (Diptera: Calliphoridae) to investigate the life history parameters at eight constant temperatures ranging from 8 to 36 °C. We also compared developmental rate of A. grahami in three groups of constant versus fluctuating temperatures: 8 °C vs. 6–12 °C, 12 °C vs. 10–16 °C, and 16 °C vs. 14–20 °C. Our data showed that A. grahami is cold tolerant with a mean (±SE) development threshold temperature (D0) of 3.41 ± 0.48 °C and a thermal summation constant (K) of 8125.2 ± 288.4-degree hours. The three groups subjected to fluctuating temperatures took longer to develop compared to those developing in constant temperatures when simulated in a model. These results not only provide detailed developmental data for the use of A. grahami in the estimation of the PMI, but also indicate that ambient temperature fluctuation must be taken into consideration for the use of all necrophagous fly species. [ABSTRACT FROM AUTHOR]