Alternaria (A.) is a genus of widespread fungi capable of producing numerous, possibly health-endangering Alternaria toxins (ATs), which are usually not the focus of attention. The formation of ATs depends on the species and complex interactions of various environmental factors and is not fully understood. In this study the influence of temperature (7 °C, 25 °C), substrate (rice, wheat kernels) and incubation time (4, 7, and 14 days) on the production of thirteen ATs and three sulfoconjugated ATs by three different Alternaria isolates from the species groups A. tenuissima and A. infectoria was determined. High-performance liquid chromatography coupled with tandem mass spectrometry was used for quantification. Under nearly all conditions, tenuazonic acid was the most extensively produced toxin. At 25 °C and with increasing incubation time all toxins were formed in high amounts by the two A. tenuissima strains on both substrates with comparable mycotoxin profiles. However, for some of the toxins, stagnation or a decrease in production was observed from day 7 to 14. As opposed to the A. tenuissima strains, the A. infectoria strain only produced low amounts of ATs, but high concentrations of stemphyltoxin III. The results provide an essential insight into the quantitative in vitro AT formation under different environmental conditions, potentially transferable to different field and storage conditions.

To predict how widely distributed species will perform under future climate change, it is crucial to understand and reveal their underlying phylogenetics. However, detailed information about plant adaptation and its genetic basis and history remains scarce and especially widely distributed species receive little attention despite their putatively high adaptability.To examine the adaptation potential of a widely distributed species, we sampled the model plant Silene vulgaris across Europe. In a greenhouse experiment, we exposed the offspring of these populations to a climate change scenario for central Europe and revealed the population structure through whole‐genome sequencing. Plants were grown under two temperatures (18°C and 21°C) and three precipitation regimes (65, 75, and 90 mm) to measure their response in biomass and fecundity‐related traits. To reveal the population genetic structure, ddRAD sequencing was employed for a whole‐genome approach. We found three major genetic clusters in S. vulgaris from Europe: one cluster comprising Southern European populations, one cluster of Western European populations, and another cluster containing central European populations. Population genetic diversity decreased with increasing latitude, and a Mantel test revealed significant correlations between F_ST and geographic distances as well as between genetic and environmental distances. Our trait analysis showed that the genetic clusters significantly differed in biomass‐related traits and in the days to flowering. However, half of the traits showed parallel response patterns to the experimental climate change scenario. Due to the differentiated but parallel response patterns, we assume that phenotypic plasticity plays an important role for the adaptation of the widely distributed species S. vulgaris and its intraspecific genetic lineages.

Climate change-induced heat waves often result in reduced seed yields and quality via high-temperature effects in the gametophytic phase. Surprisingly, the ability of pollen and ovules, particularly among wild plant populations, to adapt or acclimate to heat stress remains poorly understood. To address this gap, we examined the adaptive and acclimation potential of six gametophytic traits in eleven distinct populations of wild Silene vulgaris across a temperature gradient in Europe. First, we cultivated plants in a common garden to reveal differences in gametophytic traits indicative of adaptation. Next, we assessed the acclimation potential of these traits to heat stress by subjecting flowering plants to two chronic heat stress (CHS) treatments: moderate (35/30 °C) and severe (40/35 °C), for 18 days. Findings from the common garden experiment indicated no intraspecific variation in gametophytic traits across the temperature gradient, suggesting that these traits may not influence the plant’s sexual adaptation to its local habitat. Plants originating from colder climates produced more and larger seeds than those from warmer climates. During CHS treatments, the female gametophyte was less temperature sensitive compared to the male gametophyte. Moderate CHS led to larger ovaries with more, large-sized ovules, while severe CHS reduced ovule numbers but increased their size. In contrast, both CHS treatments decreased pollen grain numbers, size, and anther length, with severe CHS causing more significant reductions. These reductions in gametophytic traits ultimately translated to lower seed yield and quality, which may threaten the sustained existence of natural plant populations over time. Under both CHS treatments, the acclimation potential did not vary among plant populations along the temperature gradient, except for pollen size under severe CHS, with larger pollen size in warmer climates than in colder regions. Our findings suggest that the lack of adaptation and acclimation mechanisms in the gametophytic traits (except for pollen size) of wild Silene vulgaris populations along the temperature gradient indicates that these plants may rely on alternative strategies, such as shifts in flowering time, to respond to thermal stress.