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Genetic basis and adaptive implications of temperature-dependent and temperature-independent effects of drought on chickpea phenology

https://doi.org/10.1101/2022.01.26.477940

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Mapping quantitative trait loci in chickpea associated with time to flowering and resistance to Didymella rabiei the causal agent of Ascochyta blight

inferredcites →https://doi.org/10.1007/s10681-014-1261-7openalex-snapshot

Allelic relationships of flowering time genes in chickpea

inferredcites →https://doi.org/10.1016/0378-4290(91)90070-copenalex-snapshot

Influence of water-deficits on phenology, growth and dry-matter allocation in chickpea (Cicer arietinum)

inferredcites →https://doi.org/10.1016/0378-4290(94)90038-8openalex-snapshot

Genotypic variation in moisture response of chickpea grown under line-source sprinklers in a semi-arid tropical environment

inferredcites →https://doi.org/10.1016/b978-0-12-417104-6.00013-3openalex-snapshot

Characterizing the crop environment – nature, significance and applications

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Maize

inferredcites →https://doi.org/10.1016/j.agrformet.2012.09.012openalex-snapshot

Climate change, phenology, and phenological control of vegetation feedbacks to the climate system

inferredcites →https://doi.org/10.1016/j.agrformet.2020.108289openalex-snapshot

Multi-model evaluation of phenology prediction for wheat in Australia

inferredcites →https://doi.org/10.1016/j.compag.2011.04.003openalex-snapshot

PhenologyMMS: A program to simulate crop phenological responses to water stress

inferredcites →https://doi.org/10.1016/j.eja.2020.126154openalex-snapshot

Modelling phenology to probe for trade-offs between frost and heat risk in lentil and faba bean

inferredcites →https://doi.org/10.1016/j.envsoft.2014.07.009openalex-snapshot

APSIM – Evolution towards a new generation of agricultural systems simulation

inferredcites →https://doi.org/10.1016/j.fcr.2006.02.007openalex-snapshot

Genotype by environment studies demonstrate the critical role of phenology in adaptation of chickpea (Cicer arietinum L.) to high and low yielding environments of India

inferredcites →https://doi.org/10.1016/j.fcr.2009.06.005openalex-snapshot

Physiology of flowering and grain filling in faba bean

inferredcites →https://doi.org/10.1016/j.fcr.2011.09.020openalex-snapshot

Temperature-stratified screening of chickpea (Cicer arietinum L.) genetic resource collections reveals very limited reproductive chilling tolerance compared to its annual wild relatives

inferredcites →https://doi.org/10.1016/j.fcr.2014.08.003openalex-snapshot

The critical period for yield determination in chickpea (Cicer arietinum L.)

inferredcites →https://doi.org/10.1016/j.fcr.2017.01.008openalex-snapshot

Characterisation of chickpea cropping systems in Australia for major abiotic production constraints

inferredcites →https://doi.org/10.1016/j.flora.2015.05.007openalex-snapshot

Phenology, leaf gas exchange, growth and seed yield in Medicago polymorpha L. populations affected by water deficit and subsequent recovery

inferredcites →https://doi.org/10.1016/j.jas.2008.07.004openalex-snapshot

Wild lentil and chickpea harvest in Israel: bearing on the origins of Near Eastern farming

inferredcites →https://doi.org/10.1016/s0065-2113(01)72012-3openalex-snapshot

Genetics of flowering time in chickpea and its bearing on productivity in semiarid environments

inferredcites →https://doi.org/10.1016/s0378-4290(03)00120-5openalex-snapshot

The effect of timing and severity of water deficit on growth, development, yield accumulation and nitrogen fixation of mungbean

inferredcites →https://doi.org/10.1016/s1161-0301(02)00108-9openalex-snapshot

An overview of APSIM, a model designed for farming systems simulation

inferredcites →https://doi.org/10.1038/166247a0openalex-snapshot

Genetical Structure of Populations

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Resequencing 50 accessions of cultivated and wild rice yields markers for identifying agronomically important genes

inferredcites →https://doi.org/10.1038/ni1410openalex-snapshot

Plant NBS-LRR proteins in pathogen sensing and host defense

inferredcites →https://doi.org/10.1038/nrg2611openalex-snapshot

Genetics in geographically structured populations: defining, estimating and interpreting FST

inferredcites →https://doi.org/10.1038/s41558-019-0417-9openalex-snapshot

Early sowing systems can boost Australian wheat yields despite recent climate change

inferredcites →https://doi.org/10.1038/s41598-019-43848-6openalex-snapshot

Accounting for soil moisture improves prediction of flowering time in chickpea and wheat

inferredcites →https://doi.org/10.1046/j.1365-2745.2001.00576.xopenalex-snapshot

Water use trade‐offs and optimal adaptations to pulse‐driven arid ecosystems

inferredcites →https://doi.org/10.1046/j.1469-8137.2002.00405.xopenalex-snapshot

Vernalization response of wild chickpea

inferredcites →https://doi.org/10.1071/ar04104openalex-snapshot

Genotype by environment studies across Australia reveal the importance of phenology for chickpea (Cicer arietinum L.) improvement

inferredcites →https://doi.org/10.1071/ar05089openalex-snapshot

Evolution in the genus Cicer—vernalisation response and low temperature pod set in chickpea (C. arietinum L.) and its annual wild relatives

inferredcites →https://doi.org/10.1071/ar07380openalex-snapshot

Identifying chickpea homoclimes using the APSIM chickpea model

inferredcites →https://doi.org/10.1071/ar9770177openalex-snapshot

Water stress and phenology in wheat

inferredcites →https://doi.org/10.1071/cp10349openalex-snapshot

An early transient water deficit reduces flower number and pod production but increases seed size in chickpea (Cicer arietinum L.)

inferredcites →https://doi.org/10.1071/cp11218openalex-snapshot

High temperature tolerance in chickpea and its implications for plant improvement

inferredcites →https://doi.org/10.1071/cp15253openalex-snapshot

Patterns of water stress and temperature for Australian chickpea production

inferredcites →https://doi.org/10.1071/cp17406openalex-snapshot

Responses to phosphorus among barley genotypes

inferredcites →https://doi.org/10.1071/fp13177openalex-snapshot

Plot size matters: interference from intergenotypic competition in plant phenotyping studies

inferredcites →https://doi.org/10.1071/fp14115openalex-snapshot

Changes in timing of water uptake and phenology favours yield gain in terminal water stressed chickpea AtDREB1A transgenics

inferredcites →https://doi.org/10.1073/pnas.1734110100openalex-snapshot

A calmodulin-binding protein from Arabidopsis has an essential role in pollen germination

inferredcites →https://doi.org/10.1080/00031305.2019.1583913openalex-snapshot

Moving to a World Beyond “ p < 0.05”

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Influence of Daylength and Night Temperature on Flowering of Gossypium

inferredcites →https://doi.org/10.1086/378927openalex-snapshot

The Chickpea, Summer Cropping, and a New Model for Pulse Domestication in the Ancient Near East

inferredcites →https://doi.org/10.1093/ae/48.2.94openalex-snapshot

Adaptation of the Western Corn Rootworm to Crop Rotation: Evolution of a New Strain in Response to a Management Practice

inferredcites →https://doi.org/10.1093/bioinformatics/btu041openalex-snapshot

ngsTools: methods for population genetics analyses from next-generation sequencing data

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AINTEGUMENTA and AINTEGUMENTA-LIKE6 directly regulate floral homeotic, growth, and vascular development genes in young Arabidopsis flowers

inferredcites →https://doi.org/10.1093/jxb/erab537openalex-snapshot

Explaining pre-emptive acclimation by linking information to plant phenotype

inferredcites →https://doi.org/10.1093/jxb/erq459openalex-snapshot

Environment characterization as an aid to wheat improvement: interpreting genotype–environment interactions by modelling water-deficit patterns in North-Eastern Australia

inferredcites →https://doi.org/10.1093/jxb/err269openalex-snapshot

Any trait or trait-related allele can confer drought tolerance: just design the right drought scenario

inferredcites →https://doi.org/10.1093/jxb/ers079openalex-snapshot

The rice ERF transcription factor OsERF922 negatively regulates resistance to Magnaporthe oryzae and salt tolerance

inferredcites →https://doi.org/10.1093/jxb/ert209openalex-snapshot

Quantification of the effects of VRN1 and Ppd-D1 to predict spring wheat (Triticum aestivum) heading time across diverse environments

inferredcites →https://doi.org/10.1093/jxb/erw221openalex-snapshot

Phenotypic plasticity and its genetic regulation for yield, nitrogen fixation and δ13C in chickpea crops under varying water regimes

inferredcites →https://doi.org/10.1093/mp/sss070openalex-snapshot

BR Signal Influences Arabidopsis Ovule and Seed Number through Regulating Related Genes Expression by BZR1

inferredcites →https://doi.org/10.1098/rspb.2017.1494openalex-snapshot

Hierarchical structure of ecological and non-ecological processes of differentiation shaped ongoing gastropod radiation in the Malawi Basin

inferredcites →https://doi.org/10.1101/gr.4252305openalex-snapshot

Genomic scans for selective sweeps using SNP data

inferredcites →https://doi.org/10.1104/pp.109.141119openalex-snapshot

AINTEGUMENTA and AINTEGUMENTA-LIKE6 Act Redundantly to Regulate Arabidopsis Floral Growth and Patterning

inferredcites →https://doi.org/10.1104/pp.109.143495openalex-snapshot

Epigenetic Regulation of Gene Programs by EMF1 and EMF2 in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.113.221911openalex-snapshot

The Arabidopsis ETHYLENE RESPONSE FACTOR1 Regulates Abiotic Stress-Responsive Gene Expression by Binding to Different cis-Acting Elements in Response to Different Stress Signals

inferredcites →https://doi.org/10.1104/pp.15.00677openalex-snapshot

Ethylene Response Factors: A Key Regulatory Hub in Hormone and Stress Signaling

inferredcites →https://doi.org/10.1105/tpc.010227openalex-snapshot

EMBRYONIC FLOWER2, a Novel Polycomb Group Protein Homolog, Mediates Shoot Development and Flowering in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.105.036871openalex-snapshot

The BAM1/BAM2 Receptor-Like Kinases Are Important Regulators ofArabidopsisEarly Anther Development

inferredcites →https://doi.org/10.1105/tpc.106.049957openalex-snapshot

EMBRYONIC FLOWER1 Participates in Polycomb Group–MediatedAGGene Silencing inArabidopsis

inferredcites →https://doi.org/10.1105/tpc.112.109090openalex-snapshot

BRANCHED1 Interacts with FLOWERING LOCUS T to Repress the Floral Transition of the Axillary Meristems in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.13.8.1865openalex-snapshot

EMF1, A Novel Protein Involved in the Control of Shoot Architecture and Flowering in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.8.2.155openalex-snapshot

AINTEGUMENTA, an APETALA2-like gene of Arabidopsis with pleiotropic roles in ovule development and floral organ growth.

inferredcites →https://doi.org/10.1111/eva.13147openalex-snapshot

Persistent panmixia despite extreme habitat loss and population decline in the threatened tricolored blackbird (Agelaius tricolor)

inferredcites →https://doi.org/10.1111/gcb.15297openalex-snapshot

Parasitoids indicate major climate‐induced shifts in arctic communities

inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02592.xopenalex-snapshot

The CLAVATA1‐related BAM1, BAM2 and BAM3 receptor kinase‐like proteins are required for meristem function in Arabidopsis

inferredcites →https://doi.org/10.1111/j.1439-0523.2003.00895.xopenalex-snapshot

Major flowering time gene and polygene effects on chickpea seed weight

inferredcites →https://doi.org/10.1111/jac.12200openalex-snapshot

Progress towards flowering of faba bean ( V icia faba L .) is more than photothermal

inferredcites →https://doi.org/10.1111/jipb.13144openalex-snapshot

ERF1 delays flowering through direct inhibition of FLOWERING LOCUS T expression in Arabidopsis

inferredcites →https://doi.org/10.1111/mec.15501openalex-snapshot

Variation in recombination rate affects detection of outliers in genome scans under neutrality

inferredcites →https://doi.org/10.1111/nph.12291openalex-snapshot

APETALA 2/Ethylene Responsive Factor ( AP 2/ ERF ) transcription factors: mediators of stress responses and developmental programs

inferredcites →https://doi.org/10.1111/pbr.12325openalex-snapshot

Vernalization response of domesticated × wild chickpea progeny is subject to strong genotype by environment interaction

inferredcites →https://doi.org/10.1139/gen-2016-0036openalex-snapshot

QTL mapping of early flowering and resistance to ascochyta blight in chickpea

inferredcites →https://doi.org/10.1146/annurev.ecolsys.37.091305.110100openalex-snapshot

Ecological and Evolutionary Responses to Recent Climate Change

inferredcites →https://doi.org/10.1186/s12859-014-0356-4openalex-snapshot

ANGSD: Analysis of Next Generation Sequencing Data

inferredcites →https://doi.org/10.1186/s13059-015-0606-4openalex-snapshot

A haplotype map of allohexaploid wheat reveals distinct patterns of selection on homoeologous genomes

inferredcites →https://doi.org/10.1198/108571106x154443openalex-snapshot

On the design of early generation variety trials with correlated data

inferredcites →https://doi.org/10.1371/journal.pone.0035995openalex-snapshot

ERF5 and ERF6 Play Redundant Roles as Positive Regulators of JA/Et-Mediated Defense against Botrytis cinerea in Arabidopsis

inferredcites →https://doi.org/10.1534/genetics.113.154740openalex-snapshot

Quantifying Population Genetic Differentiation from Next-Generation Sequencing Data

inferredcites →https://doi.org/10.20935/al102openalex-snapshot

Climates Multiple: Three Baselines, Two Tolerances, One Normal

inferredcites →https://doi.org/10.2135/cropsci2002.0122openalex-snapshot

Improving Intrinsic Water-Use Efficiency and Crop Yield

inferredcites →https://doi.org/10.3389/fgene.2018.00547openalex-snapshot

Dynamical Modeling of the Core Gene Network Controlling Flowering Suggests Cumulative Activation From the FLOWERING LOCUS T Gene Homologs in Chickpea

inferredcites →https://doi.org/10.3389/fpls.2016.00478openalex-snapshot

Determination of Photoperiod-Sensitive Phase in Chickpea (Cicer arietinum L.)

inferredcites →https://doi.org/10.3389/fpls.2017.00359openalex-snapshot

Genome Analysis Identified Novel Candidate Genes for Ascochyta Blight Resistance in Chickpea Using Whole Genome Re-sequencing Data

inferredcites →https://doi.org/10.3389/fpls.2021.635397openalex-snapshot

The WtmsDW Locus on Wheat Chromosome 2B Controls Major Natural Variation for Floret Sterility Responses to Heat Stress at Booting Stage

inferredcites →https://doi.org/10.4161/psb.29115openalex-snapshot

HAESA and HAESA-LIKE2 activate organ abscission downstream of NEVERSHED and EVERSHED inArabidopsisflowers

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1007/s11032-026-01701-5openalex-snapshot

Genetic interactions among flowering loci influence phenology, vigour, and yield in chickpea

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