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Salt tolerance variability among stress‐selected Panicum coloratum cv. Klein plants
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/j.1537-2197.1996.tb12811.xopenalex-snapshot
Intraspecific variation in salt tolerance and morphology in the coastal grass spartina patens (poaceae)
inferredcites →https://doi.org/10.1006/anbo.1999.0912openalex-snapshot
K+Nutrition and Na+Toxicity: The Basis of Cellular K+/Na+Ratios
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Kinematic Analysis of Cell Division and Expansion
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Rapid determination of free proline for water-stress studies
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Rapid assay for determination of water soluble quaternary ammonium compounds
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Anchored simple-sequence repeats as primers to generate species-specific DNA markers in Lolium and Festuca grasses
inferredcites →https://doi.org/10.1007/s10722-013-9982-3openalex-snapshot
Collection and morphological characterization of Panicum coloratum L. in Argentina
inferredcites →https://doi.org/10.1007/s12229-015-9153-7openalex-snapshot
Salt Glands in the Poaceae Family and Their Relationship to Salinity Tolerance
inferredcites →https://doi.org/10.1016/0022-5193(65)90077-9openalex-snapshot
An analysis of irreversible plant cell elongation
inferredcites →https://doi.org/10.1016/0304-3746(78)90007-0openalex-snapshot
Tropical pasture and fodder plants
inferredcites →https://doi.org/10.1016/j.copbio.2010.03.002openalex-snapshot
More from less: plant growth under limited water
inferredcites →https://doi.org/10.1016/j.envexpbot.2012.07.009openalex-snapshot
Ecophysiology of Pennisetum clandestinum: a valuable salt tolerant grass
inferredcites →https://doi.org/10.1016/j.jplph.2009.03.015openalex-snapshot
Leaf expansion in grasses under salt stress
inferredcites →https://doi.org/10.1016/j.plantsci.2003.10.024openalex-snapshot
Potential biochemical indicators of salinity tolerance in plants
inferredcites →https://doi.org/10.1016/j.tplants.2012.02.003openalex-snapshot
Leaf size control: complex coordination of cell division and expansion
inferredcites →https://doi.org/10.1016/s0098-8472(01)00100-9openalex-snapshot
Species and population variation to salinity stress in Panicum hemitomon, Spartina patens, and Spartina alterniflora: morphological and physiological constraints
inferredcites →https://doi.org/10.1016/s0925-8574(96)00251-0openalex-snapshot
Population variation in growth response to flooding of three marsh grasses
inferredcites →https://doi.org/10.1016/s0958-1669(02)00298-7openalex-snapshot
Engineering salt tolerance in plants
inferredcites →https://doi.org/10.1023/a:1020691618797openalex-snapshot
Inter simple sequence repeat (ISSR) polymorphism and its application in plant breeding
inferredcites →https://doi.org/10.1023/a:1024553303144openalex-snapshot
Screening methods for salinity tolerance: a case study with tetraploid wheat
inferredcites →https://doi.org/10.1038/nbt.2120openalex-snapshot
Wheat grain yield on saline soils is improved by an ancestral Na+ transporter gene
inferredcites →https://doi.org/10.1046/j.1365-2494.1998.00139.xopenalex-snapshot
Salinity effects on the early development stages of Panicum coloratum: cultivar differences
inferredcites →https://doi.org/10.1046/j.1365-3040.1998.00319.xopenalex-snapshot
Is thermal time adequate for expressing the effects of temperature on sunflower leaf development?
inferredcites →https://doi.org/10.1046/j.1439-0523.2000.00504.xopenalex-snapshot
Oxidative stress indicators as selection tools for salt tolerance
inferredcites →https://doi.org/10.1071/ar01167openalex-snapshot
Physiological causes for decreased productivity under high salinity in Boma, a tetraploid Chloris gayana cultivar. II. Oxidative stress
inferredcites →https://doi.org/10.1071/bt9740057openalex-snapshot
The Cytology, Breeding System and Flowering Behaviour of Panicum coloratum
inferredcites →https://doi.org/10.1071/ea9860181openalex-snapshot
Salt tolerance of some tropical pasture legumes with potential adaptation to cracking clay soils.
inferredcites →https://doi.org/10.1071/pp9860161openalex-snapshot
Salinity Resistance in Rice ( Oryza sativa L.) And a Pyramiding Approach to Breeding Varieties for Saline Soils
inferredcites →https://doi.org/10.1086/283244openalex-snapshot
Evidence for the Existence of Three Primary Strategies in Plants and Its Relevance to Ecological and Evolutionary Theory
inferredcites →https://doi.org/10.1093/aob/mcs026openalex-snapshot
Advanced phenotyping offers opportunities for improved breeding of forage and turf species
inferredcites →https://doi.org/10.1093/jxb/42.8.1003openalex-snapshot
Stomatal and Mesophyll Limitations of Photosynthesis in Phosphate Deficient Sunflower, Maize and Wheat Plants
inferredcites →https://doi.org/10.1093/jxb/47.11.1651openalex-snapshot
Effects of soil resistance to root penetration on leaf expansion in wheat (Triticum aestivumL.): composition, number and size of epidermal cells in mature blades
inferredcites →https://doi.org/10.1093/jxb/47.3.339openalex-snapshot
An analysis of relative elemental growth rate, epidermal cell size and xyloglucan endotransglycosylase activity through the growing zone of ageing maize leaves
inferredcites →https://doi.org/10.1093/jxb/erj108openalex-snapshot
World salinization with emphasis on Australia
inferredcites →https://doi.org/10.1093/jxb/erl168openalex-snapshot
Why are Chloris gayana leaves shorter in salt-affected plants? Analyses in the elongation zone
inferredcites →https://doi.org/10.1093/jxb/ern087openalex-snapshot
Genetic variability for leaf growth rate and duration under water deficit in sunflower: analysis of responses at cell, organ, and plant level
inferredcites →https://doi.org/10.1104/pp.103.4.1107openalex-snapshot
Kinematics and Dynamics of Sorghum (Sorghum bicolor L.) Leaf Development at Various Na/Ca Salinities (I. Elongation Growth)
inferredcites →https://doi.org/10.1104/pp.105.1.191openalex-snapshot
Nitrogen Use within the Growing Leaf Blade of Tall Fescue
inferredcites →https://doi.org/10.1104/pp.106.079699openalex-snapshot
Phosphorus Deficiency Decreases Cell Division and Elongation in Grass Leaves
inferredcites →https://doi.org/10.1104/pp.106.093948openalex-snapshot
Cold Nights Impair Leaf Growth and Cell Cycle Progression in Maize through Transcriptional Changes of Cell Cycle Genes
inferredcites →https://doi.org/10.1104/pp.124.2.845openalex-snapshot
Can Meristematic Activity Determine Variation in Leaf Size and Elongation Rate among Four Poa Species? A Kinematic Study
inferredcites →https://doi.org/10.1104/pp.85.1.290openalex-snapshot
Assessment of Spatial Distribution of Growth in the Elongation Zone of Grass Leaf Blades
inferredcites →https://doi.org/10.1104/pp.88.1.233openalex-snapshot
Salinity Stress Inhibits Bean Leaf Expansion by Reducing Turgor, Not Wall Extensibility
inferredcites →https://doi.org/10.1104/pp.90.2.708openalex-snapshot
Growth Patterns Inferred from Anatomical Records
inferredcites →https://doi.org/10.1111/j.1365-2494.2010.00768.xopenalex-snapshot
Variability in salt tolerance of native populations of Elymus scabrifolius (Döll) J. H. Hunz from Argentina
inferredcites →https://doi.org/10.1111/j.1365-3040.1989.tb01957.xopenalex-snapshot
Nitrate availability and shoot area development in small willow (Salix viminalis)
inferredcites →https://doi.org/10.1111/j.1365-3040.2004.01194.xopenalex-snapshot
The decrease in growth of phosphorus‐deficient maize leaves is related to a lower cell production
inferredcites →https://doi.org/10.1111/j.1365-3040.2006.01595.xopenalex-snapshot
Plasticity to soil water deficit in Arabidopsis thaliana: dissection of leaf development into underlying growth dynamic and cellular variables reveals invisible phenotypes
inferredcites →https://doi.org/10.1111/j.1365-3040.2008.01787.xopenalex-snapshot
Nitrogen deficiency inhibits leaf blade growth in Lolium perenne by increasing cell cycle duration and decreasing mitotic and post‐mitotic growth rates
inferredcites →https://doi.org/10.1111/j.1365-3040.2008.01916.xopenalex-snapshot
Quantifying the three main components of salinity tolerance in cereals
inferredcites →https://doi.org/10.1111/j.1466-8238.2008.00403.xopenalex-snapshot
Soil salinity determines the relative abundance of C3/C4 species in Argentinean grasslands
inferredcites →https://doi.org/10.1111/j.1469-8137.1989.tb00356.xopenalex-snapshot
Ecological genetics of salt resistance in the clonal perennial, Agrostis stolonifera L.
inferredcites →https://doi.org/10.1111/j.1601-5223.2003.01800.xopenalex-snapshot
Inter simple sequence repeat (ISSR) analysis of genetic diversity in tef [Eragrostis tef (Zucc.) Trotter]
inferredcites →https://doi.org/10.1111/j.1744-7909.2007.00379.xopenalex-snapshot
Spatial and Temporal Quantitative Analysis of Cell Division and Elongation Rate in Growing Wheat Leaves under Saline Conditions
inferredcites →https://doi.org/10.1146/annurev.arplant.59.032607.092819openalex-snapshot
Environmental Effects on Spatial and Temporal Patterns of Leaf and Root Growth
inferredcites →https://doi.org/10.1146/annurev.arplant.59.032607.092911openalex-snapshot
Mechanisms of Salinity Tolerance
inferredcites →https://doi.org/10.1146/annurev.cellbio.13.1.171openalex-snapshot
ASSEMBLY AND ENLARGEMENT OF THE PRIMARY CELL WALL IN PLANTS
inferredcites →https://doi.org/10.1186/1746-4811-8-7openalex-snapshot
Identifying biological landmarks using a novel cell measuring image analysis tool: Cell-o-Tape
inferredcites →https://doi.org/10.2135/cropsci1981.0011183x002100030007xopenalex-snapshot
Cell Dynamics in Leaf Meristems of Contrasting Tall Fescue Genotypes1
inferredcites →https://doi.org/10.2136/sssaj2000.641359xopenalex-snapshot
Salinity–Grain Yield Response Functions of Barley Cultivars Assessed with a Drip‐Injection Irrigation System
inferredcites →https://doi.org/10.2307/2260647openalex-snapshot
The Physiology of Plants Under Stress.
inferredcites →https://doi.org/10.2307/3899429openalex-snapshot
Forages: The Science of Grassland Agriculture
inferredcites →https://doi.org/10.3732/ajb.93.12.1784openalex-snapshot
Salt tolerance and osmotic adjustment of Spartina alterniflora (Poaceae) and the invasive M haplotype of Phragmites australis (Poaceae) along a salinity gradient
inferredcites →https://doi.org/10.3923/pjbs.2008.1161.1164openalex-snapshot
Ultrastructural Changes in Shoot Apical Meristem of Canola (Brassica napus cv. Symbol) Treated with Sodium Chloride
inferredcites →https://doi.org/10.4067/s0365-28072006000400006openalex-snapshot
Dinámica de Acumulación de Láminas Foliares y Estructura del Forraje Diferido de Panicum coloratum L.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2017.04.016zenodo-depositor-declared
Evaluation of proline functions in saline conditions
inferred← citeshttps://doi.org/10.1007/978-3-030-52592-7_19openalex-snapshot
Plant Tolerance Mechanisms to Soil Salinity Contribute to the Expansion of Agriculture and Livestock Production in Argentina
inferred← citeshttps://doi.org/10.1007/s10722-022-01530-3openalex-snapshot
Intraspecific differentiation in genetic structure in Panicum coloratum L.: importance for germplasm conservation and breeding
inferred← citeshttps://doi.org/10.1007/s10722-026-02879-5openalex-snapshot
Intraspecific variation in tolerance to salinity, hypoxia and their combination in a Panicum coloratum var. coloratum germplasm collection
inferred← citeshttps://doi.org/10.1007/s11738-017-2357-1openalex-snapshot
Glycinebetaine in saline conditions: an assessment of the current state of knowledge
inferred← citeshttps://doi.org/10.1016/bs.agron.2021.03.001openalex-snapshot
Critical knowledge gaps and research priorities in global soil salinity
inferred← citeshttps://doi.org/10.1016/j.aoas.2022.12.005openalex-snapshot
Salinity tolerance determination in four sunflower (Helianthus annuus L.) hybrids using yield parameters and principal components analysis model
inferred← citeshttps://doi.org/10.1039/d2gc04796aopenalex-snapshot
Natural multi-osmolyte cocktails form deep eutectic systems of unprecedented complexity: discovery, affordances and perspectives
inferred← citeshttps://doi.org/10.1111/aab.12733openalex-snapshot
Combined effect of salinity and hypoxia in seedlings of two varieties of Panicum coloratum : Morphology, root system architecture, oxidative damage and antioxidant response
inferred← citeshttps://doi.org/10.1111/gfs.12263openalex-snapshot
Nutrient deficiency and hypoxia as constraints to Panicum coloratum growth in alkaline soils
inferred← citeshttps://doi.org/10.1111/pbr.13293openalex-snapshot
Differences Between Phenotypic Selection Methods in Two Botanical Varieties of Panicum coloratum L. (Kleingrass) to Increase Forage Production Under Saline‐Hypoxic Conditions
inferred← citeshttps://doi.org/10.17138/tgft(11)233-239openalex-snapshot
Nitrogen fertilization effects on forage production and nutritive value of 4 tropical grasses on alkaline soils in Argentina
inferred← citeshttps://doi.org/10.17138/tgft(6)117-176openalex-snapshot
Tropical Grasslands-Forrajes Tropicales Vol.6 No.3 [September 2018]
inferred← citeshttps://doi.org/10.17138/tgft(6)134-147openalex-snapshot
Variability for salt tolerance in a collection of Panicum coloratum var. makarikariense during early growth stages
inferred← citeshttps://doi.org/10.17138/tgft(9)144-248openalex-snapshot
Tropical Grasslands-Forrajes Tropicales Vol.9 No.2
inferred← citeshttps://doi.org/10.17138/tgft(9)171-181openalex-snapshot
Prospective genetic gain to improve salinity tolerance in a population of Panicum coloratum var. coloratum with two different selection methods
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1945485/v1openalex-snapshot
Physiological and biochemical contrasting responses associated with growth performances in sunflower seedlings after a cold stress
inferred← citeshttps://doi.org/10.3389/fpls.2022.1019169openalex-snapshot
Natural variation in growth and leaf ion homeostasis in response to salinity stress in Panicum hallii
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