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EDITORIAL article

Front. Plant Sci., 08 January 2026

Sec. Plant Abiotic Stress

Volume 16 - 2025 | https://doi.org/10.3389/fpls.2025.1757791

This article is part of the Research TopicSurviving and Thriving: How Crops Perceive and Respond to Temperature Stress Volume IIView all 9 articles

Editorial: Surviving and thriving: how crops perceive and respond to temperature stress, volume II

  • 1State Key Laboratory of Aridland Crop Science, Gansu Agricultural University, Lanzhou, China
  • 2College of Life Science and Technology, Gansu Agricultural University, Lanzhou, China
  • 3State Key Laboratory of Efficient Production of Forest Resources, Yinchuan, China
  • 4Beijing Key Laboratory of Grape Science and Enology, Chinese Academy of Sciences (CAS) Key Laboratory of Plant Resources, Institute of Botany, Chinese Academy of Sciences, Beijing, China
  • 5School of Agriculture, Food, and Wine, Waite Research Institute, Adelaide University, Urrbrae, SA, Australia

Climate change is reshaping global agroecosystems, with extreme heat and cold events emerging as major constraints on crop productivity and food security (Zhu, 2016; Jin et al., 2024; Mittler et al., 2025). Understanding how plants perceive and adapt to temperature anomalies has never been more urgent. This second volume of Surviving and Thriving: How Crops Perceive and Respond to Temperature Stress advances that mission, exploring molecular and physiological mechanisms underpinning resilience. Building on the success of the first volume (Wang et al., 2025), which featured 12 original studies across cereals, legumes, vegetables, and fiber crops, this edition adds eight new contributions. These studies broaden the phylogenetic scope to include an alternative oilseed, a cereal, a tropical perennial, and an emerging fiber nettle crop, deepening our understanding of temperature stress adaptation across diverse plant lineages (Figure 1).

Figure 1
A botanical collage of seven diverse species labeled A to G. A: Camelina with small yellow buds. B: A green wheat spike. C: A textured foxtail millet flower head. D: An Areca palm with yellow fruits. E: A potato plant with purple flowers. F: Feathery Siberian hemp nettle foliage. G: Drooping white snowdrops. The collection showcases a wide variety of leaf shapes, flowering structures, and growth forms from different plant families.

Figure 1. An Illustration of phylogenetic breadth, highlighting major, emerging and underutilized species across global agroecosystems featured in this topic. (A) Gold-of-pleasure (Camelina sativa, Brassicaceae), (B) Wheat (Triticum aestivum, Poaceae) (C) Foxtail millet (Setaria italica, Poaceae) (D) Areca palm (Areca catechu, Arecaceae) (E) Potato (Solanum tuberosum, Solanaceae) (F) Siberian hemp nettle (Urtica cannabina, Urticaceae) (G) Snowdrop (Galanthus nivalis, Amaryllidaceae). All images were sourced and adapted from iNaturalist under the Creative Commons CCO 1.0 Universal Public Domain Dedication. No additional permissions were required.

Beginning in the Mediterranean basin, where prolonged summer heat increasingly coincides with reproduction, Camelina sativa has become a model for studying thermal stress at critical reproductive stages (Figure 1A). Alberghini et al. investigated two cultivars by imposing a five-day heat treatment at the end-of-flowering (Exp1) and end-of-silique formation (Exp2). Exp1 affected growth and yield, while Exp2 influenced oil quality and tocopherol accumulation. Both stresses reduced oil content, but late stress likely triggered an antioxidant surge implicated in membrane and photosystem stabilization. This response involved trade-offs, as oil content fell by 10–12% and fatty acid profiles shifted, suggesting diversion from storage lipids to protective mechanisms. Future breeding efforts should prioritize genotypes that withstand stage-specific heat stress common in Mediterranean climates, while maintaining high yield and robust nutritional quality.

Moving northeast into the temperate wheat belt, genomic dissection of CONSTANS-like transcription factors (COL) has become central to understanding resilience in wheat (Figure 1B). Gao et al. catalogued 51 COL genes in wheat, clustered them into three subfamilies with conserved domains, and assessed their evolutionary conservation across grasses (Poaceae). Integrated analyses spanning promoter motif landscapes, expression profiles, co-expression networks, and functional assays converge on Ta-5D-COL16, a nuclear-localized activator that ties flowering progression to environmental adaptation. As photoperiod and temperature patterns shift, COL genes offer precise targets to fine-tune flowering and stress resilience without sacrificing yield.

South and inland into semi-arid Asian drylands, foxtail millet (Setaria italica) faces episodic cold that undercuts productivity (Figure 1C). Yang et al. prioritized a cold-responsive SiCST1, a nuclear protein with a ribonuclease H-like domain, by comparative transcriptomics. Cross-species validation encompassing CRISPR/Cas9 knockout of the rice homolog severely impaired cold tolerance, an effect reversed by complementation, underscoring functional conservation. Protein interaction assays place SiCST1 alongside SiOFP1 (an OVATE family protein) within a brassinolide (BR) signaling. A mechanistic model where cold-induced SiCST1 modulates BR pathway components to rebalance growth-defense trade-offs, stabilizing cellular function when temperatures dip was put forth. For highland and steppe margins where planting windows are narrow, BR-focused modulation offers a route to cold-hardy millet.

Crossing the South China Sea to Hainan Island, the tropical palm Areca catechu reveals how a warmth-adapted species copes with rare chills (Figure 1D). Thriving at 20-25°C, occasional drops to 6.8 °C exposes A. catechu to cold damage in the region. Li et al. combined physiological and transcriptomic analyses to reveal a biphasic cold acclimation: an early ROS surge activates peroxidases, while chlorophyll levels stabilize, indicating photosystem protection rather than collapse. Thousands of cold-responsive genes were identified. Network analysis identified 25 modules and six hub genes linked to chromatin remodeling, lipid signaling, and cell-wall restructuring, offering transcriptomic insights that provide subtropical plant breeders a roadmap for marker-assisted selection and microclimate management.

Across temperate zones, the world’s staple potato (Solanum tuberosum) is increasingly exposed to rising thermal loads, threatening yield stability (Figure 1E). Two consecutive studies by Zhu et al. identified two Group II WRKY factors, StWRKY65 and StWRKY75, as central integrators of thermotolerance. Overexpression of either StWRKY65 and StWRKY75 improve vegetative growth and tuber yield, elevates chlorophyll, or enhances photosynthetic metrics (photosynthesis, transpiration, stomatal conductance), while reducing H2O2 and malondialdehyde (two key molecular signatures of oxidative damage). StWRKY75 further upregulates heat shock proteins, reinforcing proteostasis. Knockdown lines of StWRKY65 and StWRKY75 also exhibited opposite effects confirming their crucial roles. For northern latitudes facing episodic heat stress, breeding strategies targeting WRKYs offer a route to sustain canopy photosynthesis and tuber development.

East across continental interiors, winter-prone plains test the limits of Urtica cannabina. In these areas, nutrient management emerges as a critical layer of defense (Figure 1F). Liu et al. showed that nitrogen and phosphorus fertilization not only mitigates freezing injury but also enhances antioxidant enzyme activity, elevates soluble sugars and proline to maintain osmotic balance, and limits oxidative damage during prolonged low-temperature exposure. Multi-omics integration points to modulation of flavonoid and phenylpropanoid biosynthetic pathways that provide ROS-scavenging metabolites while network analysis highlights hub gene modules that can be co-targeted by breeding and nutrient regimes. In regions with otherwise occasional cold spells during otherwise mild winters, nutrient-mediated priming may help strengthen plants beyond genetic improvements.

Ultimately, validation of resilience requires testing under field conditions where crops encounter natural environmental variability. Hauser et al. presented an innovative low-cost, semi-controlled field warming platform that elevates temperatures while preserving natural variability. Validated on Arabidopsis and tomato, and notably on snowdrop (Galanthus nivalis), a threatened ornamental species on the global International Union for Conservation of Nature Red List (Figure 1G), this platform enables phenotypic assessment (e.g. flowering time) under realistic diurnal and seasonal dynamics. This innovative platform, with detailed construction plans and software code, supports climate adaptation studies in major crops like wheat, while enabling research on underutilized species in remote and resource-limited environments.

Summary

These contributions deepen our understanding of how plants respond to temperature stress across diverse agroecosystems. As climate change intensifies, failure to adapt or migrate will drive local plant extinctions, with altered flowering times disrupting pollination services and triggering cascading effects that undermine ecosystem stability and resilience (Christmas et al., 2016; Wong et al., 2023). This underscores the urgency of integrating molecular insights with field-ready innovations to build climate-resilient agroecosystems, secure food supplies, and protect biodiversity.

Author contributions

ZW: Writing – original draft, Writing – review & editing. YW: Writing – original draft, Writing – review & editing. DW: Conceptualization, Writing – original draft.

Funding

The author(s) declared that financial support was received for this work and/or its publication. This Research Program was financially supported by The Research Program Sponsored by State Key Laboratory of Aridland Crop Science, Gansu Agricultural University (No. GSCS-2023-04 and GSCS-2022-03), Young Doctoral Fund by Education Department of Gansu Province (2025QB-050), Gansu Agricultural University Science and Technology Innovation Fund (GAU-QDFC-2025-02), The Undergraduate Scientific Research Training (SIETP) Program (202510733006, S202510733053), the National Natural Science Foundation of China (32260518), and The Scientific Research Start-up Fund by Gansu Agricultural University (GAUKYQD2020-26). DW acknowledges support from Adelaide University through a Future Making Fellowship.

Conflict of interest

The authors declared that this work was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

The authors ZW, DW declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.

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References

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Keywords: agroecosystem stability, climate-smart agriculture, crop resilience, flowering time, heat and cold stresses, molecular adaptation, phenology shifts, temperature stress

Citation: Wang Z, Wang Y and Wong DCJ (2026) Editorial: Surviving and thriving: how crops perceive and respond to temperature stress, volume II. Front. Plant Sci. 16:1757791. doi: 10.3389/fpls.2025.1757791

Received: 01 December 2025; Accepted: 16 December 2025; Revised: 12 December 2025;
Published: 08 January 2026.

Edited and reviewed by:

Muthusamy Ramakrishnan, Nanjing Forestry University, China

Copyright © 2026 Wang, Wang and Wong. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Zemin Wang, d3ptNDA2NDMzMjU0QDEyNi5jb20=; Darren Chern Jan Wong, ZGFycmVuLndvbmdAYWRlbGFpZGUuZWR1LmF1; d29uZ2RjakBnbWFpbC5jb20=

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.