Given the rising frequency of thermal extremes (heatwaves and cold snaps) due to climate change, comprehending how a plant’s origin affects its thermal tolerance breadth becomes vital. We studied juvenile plants from three biomes: temperate coastal rainforest, desert, and alpine. In controlled settings, plants underwent hot days and cold nights in a factorial design to examine thermal tolerance acclimation. We assessed thermal thresholds (T_crit-hot and T_crit-cold) and thermal tolerance breadth (TTB). We hypothesised that: 1) desert species would show the highest heat tolerance, alpine the greatest cold tolerance, with temperate species intermediate; 2) all species would increase heat tolerance post hot days and cold tolerance after cold nights; 3) combined exposure would broaden TTB more than individual conditions, especially in desert and alpine species. We found that biome responses were minor compared to the responses to the extreme temperature treatments. All plants increased thermal tolerance in response to hot 40°C days (T_crit-hot increased by ~3.5°C) but there was minimal change in T_crit-cold in response to the cold -2°C nights. In contrast, when exposed to both hot days and cold nights, on average plants exhibited an antagonistic response in TTB, where cold tolerance decreased and heat tolerance was reduced, and so we did not see the bi-directional expansion we hypothesised. There was, however, considerable variation among species in these responses. As climate change intensifies, plant communities, especially in transitional seasons, will regularly face such temperature swings. Our results shed light on potential plant responses under these extremes, emphasizing the need for deeper species-specific thermal acclimation insights, ultimately guiding conservation efforts.

Title: Methods for Assessing Thermal Tolerance in Plants from Different Australian Biomes

Summary: This study compared the responses of plants from temperate rainforest, alpine, and desert biomes in Australia to hot days and cold nights using temperature-dependent increases in chlorophyll a fluorescence. For each biome, eight species were selected based on seed availability and family representation. Seeds were obtained from conservation seed banks, sown, and grown under common conditions in glasshouses. Some species were purchased from nurseries.

A fully factorial experimental design was used with three biomes, eight species per biome, five replicates, and four temperature treatments (control, hot days, cold nights, and a combination of hot days and cold nights). Experiments were conducted in growth chambers, and plants were exposed to the temperature regimes for five days. Leaf temperatures were monitored using thermocouples.

Thermal tolerance assays were performed on days three and five of the experiment using Maxi Pulse Amplitude Modulating (PAM) systems. Leaf discs were placed on Peltier plates and subjected to cooling (-25°C) and heating (65°C) ramps. The critical temperatures during heating (Tcrit-hot) and cooling (Tcrit-cold) were defined as the breakpoint between the slow and fast-rise phases of basal fluorescence.