ReviewJournal of experimental botany2026
From chill to bloom: seasonal coordination of reproductive development in peach and temperate fruit trees.
Review in Journal of experimental botany, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Flowering Newsletter Editorial 2026.Journal of experimental botany · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
Abstract
Seasonal temperature is the primary environmental cue controlling reproductive development in temperate fruit trees, yet its role has largely been interpreted through dormancy-based models that view winter cold as a passive prerequisite for growth resumption. This review reassesses this framework by examining cold and warmth as sequential developmental signals acting during late flower development, after inflorescence meristem identity has been established. Integrating anatomical, cytological, and transcriptomic evidence, we show that reproductive development follows a biphasic thermal organization. Microsporogenesis can progress during winter under chilling temperatures in a species-dependent manner, with peach representing a clear case of cold-driven meiotic progression. In contrast, pollen maturation and female gametophyte development remain dependent on rising spring temperatures and occur within a narrow pre-bloom window across major Rosaceae fruit crops. We further discuss how this sequential thermal control is coordinated by multiple regulatory layers involving transcriptional regulation, hormonal balance, carbohydrate metabolism, and chromatin dynamics. Disruption of the sequence of cold and warm periods under recent climate variability uncouples male and female gametophyte development, leading to recurrent failure modes that compromise fertility. We conclude that winter represents an active developmental phase and that reproductive vulnerability arises primarily from altered thermal sequencing rather than cumulative temperature deficits.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.