PCD maintains editorial independence to ensure decisions are based on scientific merit and developmental impact.

PCD enforces publication ethics to protect the integrity of plant science.

Authorship transparency is required for all submissions.

Policy updates are documented to keep standards current.

Summaries connecting cellular mechanisms to crop outcomes strengthen impact.

Describe controls for hormone treatments and concentration gradients.

Describe batch effects and correction methods in imaging or sequencing data.

Explain how sample sizes were determined for developmental assays.

Clarify whether findings generalize across species or cultivars.

Document imaging time points and resolution settings.

Clarify cell cycle staging methods and validation.

Summarize implications for plant development and resilience research.

Clarify how pathway annotations were validated.

Explain how statistical power was assessed.

Document how cell wall composition was quantified.

Clarify how replicates were balanced across treatments.

Report how phenotypic scoring was blinded or verified.

Provide guidance on reuse of imaging datasets.

Corrections and retractions are issued to maintain transparency.

Conflicts of interest must be declared to protect trust.

Clear reporting of cell lineage methods improves reproducibility across plant models.

Report statistical thresholds used for gene expression or omics analysis.

Provide uncertainty measures for key developmental outcomes.

Clarify temperature and light regimes for growth experiments.

Report statistical corrections for multiple testing in omics data.

Explain how missing data were handled in longitudinal growth studies.

Explain how phenotype scoring was validated.

Report how anatomical sections were prepared and stained.

Include key assumptions in developmental models.

Describe how data deposition supports future reuse.

State limits of detection for imaging or molecular assays.

Explain the choice of plant model and developmental stage.

Include brief notes on growth chamber calibration.

Summarize key limitations and mitigation strategies.

Include notes on reference genomes and annotation versions.

Data integrity and ethical handling are prioritized throughout review.

Appeals are reviewed by senior editors with documented outcomes.

Document growth conditions and photoperiods to contextualize cellular responses.

Include details on sample preparation and tissue handling to avoid bias.

Explain how confounders were handled in observational plant studies.

Include references to standards or plant nomenclature guidance.

Provide a rationale for selected markers or reporter lines.

Report effect sizes relative to developmental benchmarks.

Provide context for translational relevance to crop improvement.

Explain how data quality checks were performed.

Report calibration routines for imaging devices.

Report time to analysis for high throughput workflows.

Describe how cross lab variability was minimized.

Describe how fluorescence thresholds were selected for imaging.

Describe any biosafety approvals for transgenic lines.

Describe how developmental timing was synchronized.

Describe how cytological staining was standardized.

Corrections, retractions, or expressions of concern are issued when needed to protect the scholarly record.

Reviewer confidentiality safeguards the integrity of peer review.

Editorial decisions prioritize methodological rigor and reproducibility.

Explain how imaging parameters were calibrated for microscopy assays.

Clarify how developmental stages were defined and verified.

Report software versions and pipelines for bioinformatics analyses.

Describe quality assurance steps for phenotyping workflows.

Discuss limitations related to tissue specificity or developmental stage.

Include details on controls for stress or nutrient treatments.

Describe replicate structure and experimental randomization.

Describe any deviations from standard protocols and their impact.

Document any external datasets used in the analysis.

Summarize implications for breeding or biotechnology.

Clarify how hormone pathway interactions were interpreted.

Report normalization steps for transcriptomics or proteomics data.

Explain how tissue specificity was validated.

Explain how data were curated for public repositories.