Reference health

Wait or escape? Contrasting submergence tolerance strategies of Rorippa amphibia, Rorippa sylvestris and their hybrid

https://doi.org/10.1093/aob/mcs059
CiteStamped reference-health badge
59/59 checkable references clean · checked 2026-07-22

Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.

5 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.

The 59 checked references that resolve
resolves10.1007/s00606-006-0415-z
Systematics and phylogeny of the Brassicaceae (Cruciferae): an overview
resolves10.1146/annurev.arplant.59.032607.092752
Flooding Stress: Acclimations and Genetic Diversity
resolves10.1016/j.pbi.2010.08.002
Life in the balance: a signaling network controlling survival of flooding
resolves10.1111/j.1469-8137.1988.tb00283.x
On the relative importance of convective and diffusive gas flows in plant aeration
resolves10.1111/j.1365-313X.2005.02563.x
Contrasting interactions between ethylene and abscisic acid in <i>Rumex</i> species differing in submergence tolerance
resolves10.1007/s00606-004-0131-5
Genetic variation and self-incompatibility within and outside a Rorippa hybrid zone (Brassicaceae)
resolves10.1017/S1477200007002411
Interspecific hybridization in <i>Rorippa</i> (Brassicaceae): Patterns and processes
resolves10.1046/j.1365-294X.2001.01341.x
Introgressive hybridization in<i>Rorippa</i>(Brassicaceae): gene flow and its consequences in natural and anthropogenic habitats
resolves10.1111/j.1438-8677.1999.tb00252.x
Adaptations to Flooding Stress: From Plant Community to Molecule
resolves10.1016/S1369-5266(02)00255-8
Enhancement of tolerance of abiotic stress by metabolic engineering of betaines and other compatible solutes
resolves10.1093/aob/mcp198
Intraspecific variation in the magnitude and pattern of flooding-induced shoot elongation in Rumex palustris
resolves10.1111/j.1469-8137.2010.03639.x
Fitness consequences of natural variation in flooding‐induced shoot elongation in <i>Rumex palustris</i>
resolves10.1105/tpc.106.043000
A Variable Cluster of Ethylene Response Factor–Like Genes Regulates Metabolic and Developmental Acclimation Responses to Submergence in Rice
resolves10.1073/pnas.252637799
Trehalose accumulation in rice plants confers high tolerance levels to different abiotic stresses
resolves10.1023/A:1024511232626
Submergence-induced petiole elongation in Rumex palustris is controlled by developmental stage and storage compounds
resolves10.1104/pp.108.2.735
Effect of Anoxia on Carbohydrate Metabolism in Rice Seedlings
resolves10.1270/jsbbs.57.305
A Major QTL Confers Rapid Internode Elongation in Response to Water Rise in Deepwater Rice
resolves10.1270/jsbbs.58.39
Mapping of three QTLs that regulate internode elongation in deepwater rice
resolves10.1038/nature08258
The ethylene response factors SNORKEL1 and SNORKEL2 allow rice to adapt to deep water
resolves10.1146/annurev.pp.36.060185.001045
Ethylene and Responses of Plants to Soil Waterlogging and Submergence
resolves10.1093/aob/mcf242
Physiological and Molecular Basis of Susceptibility and Tolerance of Rice Plants to Complete Submergence
resolves10.2307/2259532
Plant Zonation on Lakeshores in Nova Scotia: A Test of the Resource Specialization Hypothesis
resolves10.1104/pp.118.4.1105
Deepwater Rice: A Model Plant to Study Stem Elongation
resolves10.1016/j.ppees.2006.10.002
Bud banks and their role in vegetative regeneration – A literature review and proposal for simple classification and assessment
resolves10.1111/j.1365-3180.2007.00608.x
Weeds that can do both tricks: vegetative versus generative regeneration of the short‐lived root‐sprouting herbs <i>Rorippa palustris</i> and <i>Barbarea vulgaris</i>
resolves10.1111/j.1438-8677.2010.00415.x
Regulatory interplay of the Sub1A and CIPK15 pathways in the regulation of α‐amylase production in flooded rice plants
resolves10.1111/j.1365-2745.2004.00957.x
Abiotic constraints at the upper boundaries of two <i>Rumex</i> species on a freshwater flooding gradient
resolves10.1104/pp.104.057299
A Genome-Wide Analysis of the Effects of Sucrose on Gene Expression in Arabidopsis Seedlings under Anoxia
resolves10.1038/415514a
Increasing risk of great floods in a changing climate
resolves10.1016/S0169-5347(01)02291-1
Arabidopsis thaliana and its wild relatives: a model system for ecology and evolution
resolves10.1093/aob/mci212
Underwater Photosynthesis in Flooded Terrestrial Plants: A Matter of Leaf Plasticity
resolves10.1111/j.1365-2745.2006.01175.x
Ecophysiological determinants of plant performance under flooding: a comparative study of seven plant families
resolves10.1093/jxb/erj015
Photosynthetic consequences of phenotypic plasticity in response to submergence: Rumex palustris as a case study
resolves10.1126/science.321.5887.330
Reinventing Rice to Feed the World
resolves10.1016/0168-9452(93)90029-Y
Plant responses to anaerobiosis
resolves10.1093/jxb/47.8.999
Anaerobic carbohydrate metabolism in wheat and barley, two anoxia-intolerant cereal seeds
resolves10.1093/aob/mcn143
Is elongation-induced leaf emergence beneficial for submerged Rumex species?
resolves10.1016/S0378-4290(02)00035-7
Submergence tolerance in rainfed lowland rice: physiological basis and prospects for cultivar improvement through marker-aided breeding
resolves10.21273/HORTSCI.18.5.698
A Method for Measuring Leaf Volume, Density, Thickness, and Internal Gas Volume
resolves10.1007/BF00399922
Effect of submergence on translocation, starch content and amylolytic activity in deep-water rice
resolves10.1007/s001140050725
Rice in deep water: "How to take heed against a sea of troubles"
resolves10.1016/j.pbi.2007.01.014
Comparative genomics in the Brassicaceae: a family-wide perspective
resolves10.1093/jxb/47.10.1551
The beneficial effect of reduced elongation growth on submergence tolerance of rice
resolves10.1038/21877
Hydrologically defined niches reveal a basis for species richness in plant communities
resolves10.1016/j.fcr.2009.04.003
Responses of SUB1 rice introgression lines to submergence in the field: Yield and grain quality
resolves10.1038/nprot.2006.232
Quantification of starch in plant tissues
resolves10.1016/j.aquabot.2009.09.005
Distribution of clonal growth forms in wetlands
resolves10.1111/j.1469-8137.2008.02547.x
Different flooding responses in<i>Rorippa amphibia</i>and<i>Rorippa sylvestris</i>, and their modes of expression in F<sub>1</sub>hybrids
resolves10.3732/ajb.1000048
Other tetraploid species and conspecific diploids as sources of genetic variation for an autotetraploid
resolves10.1111/j.1365-3040.1990.tb02144.x
Aerenchyma formation and associated oxygen movement in seminal and nodal roots of wheat
resolves10.1111/j.0030-1299.2004.13083.x
Is tolerance to summer flooding correlated with distribution patterns in river floodplains? A comparative study of 20 terrestrial grassland species
resolves10.1111/j.1570-7458.2008.00722.x
Reciprocal interactions between the cabbage root fly (<i>Delia radicum</i>) and two glucosinolate phenotypes of <i>Barbarea vulgaris</i>
resolves10.1111/j.1469-8137.2010.03552.x
Natural variation of submergence tolerance among <i>Arabidopsis thaliana</i> accessions
resolves10.1046/j.1365-2745.2003.00749.x
Extreme flooding events on the Rhine and the survival and distribution of riparian plant species
resolves10.1007/BF02803993
Hormone sensitivity and plant adaptations to flooding
resolves10.1093/aob/mcf116
Interactions Between Plant Hormones Regulate Submergence-induced Shoot Elongation in the Flooding-tolerant Dicot Rumex palustris
resolves10.1111/j.1469-8137.2006.01692.x
How plants cope with complete submergence
resolves10.1111/j.1365-313X.2005.02477.x
Ethylene regulates fast apoplastic acidification and expansin A transcription during submergence‐induced petiole elongation in <i>Rumex palustris</i>
resolves10.1038/nature04920
Sub1A is an ethylene-response-factor-like gene that confers submergence tolerance to rice
The 5 references without a DOI — listed, not checked
no DOI — not checkedStudies in the North-West European species of Rorippa s. str
no DOI — not checkedAnalysis of relative gene expression data using real-time quantitative PCR and the 2-DDCT method
no DOI — not checkedMolecular cloning: a laboratory manual
no DOI — not checkedThe extraction of total RNA by the detergent and phenol method
no DOI — not checkedEthylene and flooding resistance: an integration of plant hormone physiology and plant ecology
What this badge says. CiteStamped means the CHECKABLE references of this work were clean at the dated check: each resolved to a known work in a public registry, and none carried a retraction notice at that time. It says nothing about the quality, findings, or importance of the work itself, and nothing about references deposited without a DOI.

checked 2026-07-22 — re-checked daily as this page is visited; titles and statuses come from Crossref and DataCite and are not part of the signed record

Embed this badge

Both snippets point at the live badge image and link back to this page. The badge re-renders from the daily check, so an embed never goes stale by more than a day of visits.

<a href="https://citestamp.com/citestamped/10.1093/aob/mcs059"><img src="https://citestamp.com/citestamped/10.1093/aob/mcs059/badge.svg" alt="CiteStamped reference-health badge" width="460" height="64"></a>
[![CiteStamped reference-health badge](https://citestamp.com/citestamped/10.1093/aob/mcs059/badge.svg)](https://citestamp.com/citestamped/10.1093/aob/mcs059)