The authors used a bottom‑up thermodynamic modelling framework to investigate how plants decode calcium signals, starting from Ca2+ binding to EF‑hand proteins and extending to higher‑order decoding modules. They identified six universal Ca2+-decoding modules that can explain variations in calcium sensitivity among kinases and provide a theoretical basis for interpreting calcium signal amplitude and frequency in plant cells.

Four barley genotypes were examined under simultaneous Fusarium culmorum infection and drought, revealing genotype-dependent Fusarium Head Blight severity and largely additive transcriptomic responses dominated by drought. Co‑expression and hormone profiling linked ABA and auxin to stress‑specific gene modules, and a multiple linear regression model accurately predicted combined‑stress gene expression from single‑stress data, suggesting modular regulation.

The study used ft1 knock‑out mutants in barley to demonstrate that the florigen homolog FT1 links vegetative and reproductive meristem development with plant metabolism, influencing source‑sink dynamics, longevity, and fertility. Loss of FT1 caused altered leaf and inflorescence determinacy, increased organ size but reduced fertility, and a transcriptional shift toward photosynthetic and carbon‑catabolism genes, while soluble sugar and starch accumulated in inflorescences, indicating diminished sink strength.

The study examined nitrogen use strategies in the model alga Chlamydomonas reinhardtii by comparing growth on ammonium, nitrate, and urea, finding similar molar nitrogen utilization efficiency under saturating conditions. Rapid nitrogen uptake and storage were demonstrated through pulse experiments, and source‑specific transcriptome analysis revealed distinct regulation of assimilation pathways and transporters, supporting a model of flexible nitrogen acquisition and storage.

The study benchmarked several sampling approaches for simultaneous profiling of root exudates and rhizosphere microbiota in soil-grown barley, revealing consistent exudate chemistry across methods but variation in root morphology and nitrogen exudation. High‑throughput amplicon sequencing and quantitative PCR showed protocol‑specific impacts on microbial composition, yet most rhizosphere-enriched microbes were captured by all approaches. The authors conclude that different protocols provide comparable integrated data, though methodological differences must be aligned with experimental objectives.

The study investigates how maternal environmental conditions, specifically temperature and light intensity, influence seed longevity in eight Arabidopsis thaliana natural accessions. Seeds developed under higher temperature (27 °C) and high light showed increased longevity, with transcriptome analysis of the Bor-4 accession revealing dynamic changes in stored mRNAs, including upregulation of antioxidant defenses and raffinose family oligosaccharides. These findings highlight the genotype‑dependent modulation of seed traits by the maternal environment.

The study investigates the evolutionary shift from archegonial to embryo‑sac reproduction by analyzing transcriptomes of Ginkgo reproductive organs and related species. It reveals that the angiosperm pollen‑tube guidance module MYB98‑CRP‑ECS is active in mature Ginkgo archegonia and that, while egg cell transcription is conserved, changes in the fate of other female gametophyte cells drove the transition, providing a molecular framework for this major reproductive evolution.

Two EMS‑induced recessive maize mutants (o1‑2995 and o1‑tan62) were identified as novel missense alleles of opaque1 that produce O1 protein yet cause more severe morphological defects, including reduced internode elongation and altered leaf and inflorescence patterning. These alleles also partially suppress the excessive tassel and ear branching of ramosa mutants, highlighting O1’s role in regulating plant stature and architecture.

A comparative physiological study of persimmon cultivars with flat (Hiratanenashi) and round (Koushimaru) fruit shapes revealed that differences in cell proliferation, cell shape, and size contribute to shape variation. Principal component analysis of elliptic Fourier descriptors tracked shape changes, while histology and transcriptome profiling identified candidate genes, including a WOX13 homeobox gene, potentially governing fruit shape development.

The study investigates the role of the Arabidopsis transcription factor AtMYB93 in sulfur (S) signaling and root development, revealing that AtMYB93 mutants exhibit altered expression of S transport and metabolism genes and increased shoot S levels, while tomato plants overexpressing SlMYB93 show reduced shoot S. Transcriptomic profiling, elemental analysis, and promoter activity assays indicate that AtMYB93 contributes to root responses to S deprivation, though functional redundancy masks clear phenotypic effects on lateral and adventitious root formation.