Plant Cell Development publishes research on plant cell growth, differentiation, organelle biogenesis, and cellular signaling. Manuscripts should connect mechanistic evidence to developmental outcomes.

Submissions may include original research, applied studies, methodological innovations, or evidence syntheses that advance plant cell development.

Provide a clear developmental analysis plan, including staging and validation steps.

Include validation steps for hormone or signaling assays.

Explain how statistical thresholds were chosen for omics results.

Provide notes on tissue dissection and handling procedures.

Document growth conditions and photoperiods to contextualize cellular responses.

Report software versions and pipelines for bioinformatics analyses.

Clarify whether findings generalize across species or cultivars.

Report how anatomical sections were prepared and stained.

Report time to analysis for high throughput workflows.

Report normalization steps for transcriptomics or proteomics data.

Provide guidance on reuse of imaging datasets.

Prepare manuscripts with structured abstract, introduction, methods, results, and discussion. Clearly connect cellular methods to developmental outcomes.

Provide concise titles and keywords that reflect the plant cell focus.

• Structured abstract with objectives and conclusions
• Clear methods with staging and analysis details
• Results with effect sizes and uncertainty
• Discussion of implications and limitations

For microscopy studies, report imaging settings, calibration, and quantification methods.

Describe how sampling bias was minimized across tissues.

Document any corrections for batch effects or plate effects.

Clarify how image segmentation and quantification were validated.

Explain how imaging parameters were calibrated for microscopy assays.

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

Explain how missing data were handled in longitudinal growth studies.

Explain how data quality checks were performed.

Summarize implications for breeding or biotechnology.

Clarify how replicates were balanced across treatments.

Include notes on reference genomes and annotation versions.

Report growth conditions, developmental staging, and analytical validation clearly. Provide enough detail for replication and cross-lab comparison.

Include code availability statements when feasible and specify software versions used in analysis.

Describe growth conditions, light cycles, and nutrient regimes in sufficient detail.

Document batch effects or seasonal variability when applicable.

Describe how developmental gradients were quantified.

Describe how growth measurements were standardized across replicates.

Summaries connecting cellular mechanisms to crop outcomes strengthen impact.

Clarify temperature and light regimes for growth experiments.

Report effect sizes relative to developmental benchmarks.

Describe any deviations from standard protocols and their impact.

Explain how statistical power was assessed.

Include brief notes on growth chamber calibration.

Describe how cytological staining was standardized.

We encourage sharing analytic code and documentation to support reproducibility and secondary analysis.

If data are restricted, describe the access request process and expected timelines.

Include data availability statements or access routes for restricted datasets.

Clarify how phenotyping data were scored and audited.

Clarify how multi-omics integration was performed.

Explain how cell fate decisions were quantified or inferred.

Report statistical thresholds used for gene expression or omics analysis.

Include references to standards or plant nomenclature guidance.

Include details on controls for stress or nutrient treatments.

Summarize implications for plant development and resilience research.

State limits of detection for imaging or molecular assays.

Describe any biosafety approvals for transgenic lines.

Report how stress treatments were staged and applied.

Use tables and figures to summarize developmental outcomes, lineage tracking, and imaging results. Provide high resolution visuals with descriptive captions.

Supplementary files may include protocols, extended results, or model scripts.

• Include units, developmental stages, and reference ranges
• Label tissues and sampling points clearly
• Ensure tables are interpretable without the main text

Define key developmental terms and abbreviations on first use.

Explain any deviations from standard protocols and their impact.

Provide guidance on data reuse and licensing where applicable.

Provide notes on sample preservation and fixation methods.

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

Describe quality assurance steps for phenotyping workflows.

Document imaging time points and resolution settings.

Include key assumptions in developmental models.

Describe how cross lab variability was minimized.

Explain how tissue specificity was validated.

Describe ethics approvals for sensitive data or field trials. For transgenic or edited lines, report approvals and stewardship practices.

Explain how regulatory standards informed the study design and interpretation.

Explain how gene expression or reporter assays were validated.

Summarize how findings inform plant development or crop improvement.

Report how phylogenetic comparisons were conducted if relevant.

Clarify how technical replicates were handled in analyses.

Clarify how developmental stages were defined and verified.

Explain how sample sizes were determined for developmental assays.

Explain how phenotype scoring was validated.

Report calibration routines for imaging devices.

Clarify how hormone pathway interactions were interpreted.

Report how phenotypic scoring was blinded or verified.

Report effect sizes, confidence intervals, and model diagnostics to support interpretation of developmental outcomes. Explain missing data handling and sensitivity analyses for key assumptions.

For multivariate models, describe feature selection, validation steps, and limitations that affect interpretation.

Summarize limitations related to cell type specificity or developmental timing.

Provide notes on imaging metadata and storage formats.

Summarize how findings align with existing plant development models.

Summarize how developmental phenotypes were scored consistently.

Describe controls for hormone treatments and concentration gradients.

Report statistical corrections for multiple testing in omics data.

Provide context for translational relevance to crop improvement.

Document any external datasets used in the analysis.

Document how cell wall composition was quantified.

Summarize key limitations and mitigation strategies.

Submit through ManuscriptZone or the Simple Submission Form. Both routes follow the same peer review workflow.

Include a cover letter summarizing scope alignment, cellular methods, and key findings.

• ManuscriptZone submission: https://oap.manuscriptzone.net/
• Simple submission form: https://openaccesspub.org/manuscript-submission-form

Report how model assumptions align with plant developmental biology.

Report how cell cycle markers were validated across tissues.

Describe how cell identity annotations were verified.

Describe how image annotations were audited for accuracy.

Provide uncertainty measures for key developmental outcomes.

Provide a rationale for selected markers or reporter lines.

Describe replicate structure and experimental randomization.

Clarify how pathway annotations were validated.

Explain the choice of plant model and developmental stage.

Describe how developmental timing was synchronized.

Accepted manuscripts undergo copyediting, layout, and proof review. Authors confirm accuracy before publication.

APC invoices are issued after acceptance. Publication proceeds after payment confirmation or approved waivers.

Provide details on lineage tracing or cell fate tracking methods.

Include details on reporter line construction or sources.

Explain how environmental variation was controlled.

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

Explain how confounders were handled in observational plant studies.

Discuss limitations related to tissue specificity or developmental stage.

Clarify cell cycle staging methods and validation.

Describe how data deposition supports future reuse.

Describe how fluorescence thresholds were selected for imaging.

Explain how data were curated for public repositories.